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Related documents:
| Haplotype counts inferred by Phase*. |
| Gene = LBP, Minimum allele freq. in ANY population= 0.000, 5 SNP, 1114 Subjects
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| Note that the haplotypes shown below comprise alleles at |
| the following SNP locations in the order show. The first column |
| is the allele position in the haplotype. The SNP column is the |
| SNP position in the reference sequence (1=first base). The RelativeOffset column |
| is the SNP offset relative to the Gene transcription start codon. |
| # | SNP | RelativeOffset |
| 1 | 1605 | -921 |
| 2 | 17119 | 14349 |
| 3 | 20294 | 17471 |
| 4 | 23297 | 20420 |
| 5 | 25627 | 22712 |
| Haplotype Frequency Sort Order | | Haplotype | All | Controls | Cases |
| ACGCT | | 904 | 40.6% | 483 | 40.6% | 421 | 40.6% |
| ATATC | | 699 | 31.4% | 367 | 30.8% | 332 | 32.0% |
| TCATC | | 147 | 6.6% | 90 | 7.6% | 57 | 5.5% |
| ACATC | | 146 | 6.6% | 75 | 6.3% | 71 | 6.8% |
| ACGCC | | 76 | 3.4% | 33 | 2.8% | 43 | 4.1% |
| TTATC | | 70 | 3.1% | 35 | 2.9% | 35 | 3.4% |
| ATGCT | | 26 | 1.2% | 14 | 1.2% | 12 | 1.2% |
| ATATT | | 26 | 1.2% | 10 | 0.8% | 16 | 1.5% |
| TCGCT | | 24 | 1.1% | 16 | 1.3% | 08 | 0.8% |
| ACACT | | 24 | 1.1% | 12 | 1.0% | 12 | 1.2% |
| ACGTC | | 23 | 1.0% | 11 | 0.9% | 12 | 1.2% |
| ACATT | | 17 | 0.8% | 14 | 1.2% | 03 | 0.3% |
| ACACC | | 14 | 0.6% | 10 | 0.8% | 04 | 0.4% |
| TCATT | | 13 | 0.6% | 06 | 0.5% | 07 | 0.7% |
| TCGCC | | 10 | 0.4% | 08 | 0.7% | 02 | 0.2% |
| ATGTC | | 03 | 0.1% | 03 | 0.3% | 00 | 0.0% |
| ATACT | | 03 | 0.1% | 03 | 0.3% | 00 | 0.0% |
| TTGTC | | 02 | 0.1% | 00 | 0.0% | 02 | 0.2% |
| TCACT | | 01 | 0.0% | 00 | 0.0% | 01 | 0.1% |
| Totals | | 2228 | | 1190 | | 1038 | |
| Haplotype Alphabetic Sort Order |
| ACACC | | 14 | 0.6% | 10 | 0.8% | 04 | 0.4% |
| ACACT | | 24 | 1.1% | 12 | 1.0% | 12 | 1.2% |
| ACATC | | 146 | 6.6% | 75 | 6.3% | 71 | 6.8% |
| ACATT | | 17 | 0.8% | 14 | 1.2% | 03 | 0.3% |
| ACGCC | | 76 | 3.4% | 33 | 2.8% | 43 | 4.1% |
| ACGCT | | 904 | 40.6% | 483 | 40.6% | 421 | 40.6% |
| ACGTC | | 23 | 1.0% | 11 | 0.9% | 12 | 1.2% |
| ATACT | | 03 | 0.1% | 03 | 0.3% | 00 | 0.0% |
| ATATC | | 699 | 31.4% | 367 | 30.8% | 332 | 32.0% |
| ATATT | | 26 | 1.2% | 10 | 0.8% | 16 | 1.5% |
| ATGCT | | 26 | 1.2% | 14 | 1.2% | 12 | 1.2% |
| ATGTC | | 03 | 0.1% | 03 | 0.3% | 00 | 0.0% |
| TCACT | | 01 | 0.0% | 00 | 0.0% | 01 | 0.1% |
| TCATC | | 147 | 6.6% | 90 | 7.6% | 57 | 5.5% |
| TCATT | | 13 | 0.6% | 06 | 0.5% | 07 | 0.7% |
| TCGCC | | 10 | 0.4% | 08 | 0.7% | 02 | 0.2% |
| TCGCT | | 24 | 1.1% | 16 | 1.3% | 08 | 0.8% |
| TTATC | | 70 | 3.1% | 35 | 2.9% | 35 | 3.4% |
| TTGTC | | 02 | 0.1% | 00 | 0.0% | 02 | 0.2% |
| Totals | | 2228 | | 1190 | | 1038 | |
Minimal SNP (shown in red italics) needed to unambiguously distinguish haplotypes seen more than once, by population group Please note that this an experimental resource which is still under test.Please email Ross Lazarus if you have comments or find any errors or anomalies Group=Cases (blocklist=[[1, 6]], snplist=[[1, 2, 3, 4, 5]]) Haplotype heterozygosity: Observed = 0.7218751, Expected = 0.9598219 Effective # Haplotypes = 3.596, Minimum #SNP to distinguish haplotypes seen more than once: 5| -921: | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | A | T | T | T | T | T | T | T | T | T | T | T | T | T | T | T | A | A | A | A | A | A | A | T | T | T | T | T |
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