Research Article
A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity
Table 5
Chromosome 20 SNPs tested for evidence of null alleles.
| SNP | Null allele | rs# | Position (bp)1 | Gene | MAF2 | Frequency | value | | BMI |
| rs6062302 | 62320968 | RTEL1 | 0.235 | 0.00775 | 0.002222 | 6 | 33.9 | rs2257440 | 62328267 | TNFRSF6B | 0.226 | 0.00724 | 0.008077 | 2 | 32.8 | rs6062498 | 62339059 | ZGPAT | 0.328 | 0.01377 | 0.005117 | 0 | ā | rs6062510 | 62372148 | SLC2A4RG | 0.308 | 0.00000 | 1.000000 | 0 | ā | rs932824 | 62380315 | ZBTB46 | 0.209 | 0.01274 | 0.000181 | 3 | 30.2 |
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Build GRCh37. Minor allele frequency estimated from our sample. Number of deletion carriers with genotype probability > 90%.
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