The document presents a table summarizing single variants significantly associated with body mass index (BMI). The table includes information on the chromosome, position, reference and alternate alleles, call rate, minor allele frequency, statistical measurement, p-value, beta value, and other details for each variant. The variants are intergenic or intronic and their nearest genes are provided. Allele frequencies from other databases are also listed.
The document presents a table summarizing single variants significantly associated with body mass index (BMI). The table includes information on the chromosome, position, reference and alternate alleles, call rate, minor allele frequency, statistical measurement, p-value, beta value, and other details for each variant. The variants are intergenic or intronic and their nearest genes are provided. Allele frequencies from other databases are also listed.
The document presents a table summarizing single variants significantly associated with body mass index (BMI). The table includes information on the chromosome, position, reference and alternate alleles, call rate, minor allele frequency, statistical measurement, p-value, beta value, and other details for each variant. The variants are intergenic or intronic and their nearest genes are provided. Allele frequencies from other databases are also listed.
The significant single variants associated with BMI
CHROM POS REF ALTCALLRATEMAF STAT P value Beta 1 92687424 A C 0.99821 0.05019 -5.5403 3.09E-08 -0.4911 1 173232447 G A 0.97176 0.01298 10.2574 1.43E-24 1.741 2 184282612 G A 0.94975 0.03605 9.6751 4.75E-22 1.033 2 184282613 C T 0.9506 0.03636 9.7808 1.70E-22 1.041 2 184282626 A G 0.95561 0.03514 11.1992 5.98E-29 1.208 3 84262560 T G 0.96713 0.02271 10.4618 1.72E-25 1.382 3 84263455 C A 0.97988 0.01282 8.2658 1.55E-16 1.395 5 28723857 G A 0.98187 0.01972 10.0834 8.38E-24 1.409 5 132122725 T C 0.98593 0.01035 8.5106 1.96E-17 1.586 6 59475537 C T 0.92633 0.01968 10.4319 2.35E-25 1.457 7 62445838 C T 0.97214 0.03546 9.6632 5.33E-22 1.01 7 145235076 C A 1 0.0375 -6.4432 1.22E-10 -0.6389 8 90392426 T C 0.97922 0.01562 9.053 1.64E-19 1.41 10 39556257 C T 0.99915 0.05582 -6.4663 1.05E-10 -0.6263 11 5181851 C A 0.96317 0.13478 -7.5439 4.94E-14 -0.4177 11 5181852 C T 0.96184 0.13428 -7.4495 1.01E-13 -0.4129 12 86587494 T C 0.99887 0.0521 -5.7157 1.12E-08 -0.4973 19 27863467 T C 0.99367 0.05418 -7.3169 2.72E-13 -0.6554 ated with BMI AF Function Nearest Gene Transcript dbSNP 0.9499 intron_variant EVI5 NM_001308248. rs4000726 0.02673 intergenic_region TNFSF4 :n.173232447G NA 0.05936 intergenic_region ZNF804A :n.184282612G NA 0.05927 intergenic_region ZNF804A :n.184282613C NA 0.05535 intergenic_region ZNF804A :n.184282626A NA 0.03839 intergenic_region CADM2 :n.84262560T> rs369036035 0.02262 intergenic_region CADM2 :n.84263455C> rs372115169 0.02843 intergenic_region CDH9 :n.28723857G> rs111534748 0.01724 intergenic_region CSF2 :n.132122725T NA 0.04521 intergenic_region PRIM2 :n.59475537C> NA 0.04449 intergenic_region ZNF727 :n.62445838C> NA 0.96251 intergenic_region TPK1 :n.145235076C rs11761202 0.02569 intergenic_region TMEM64 :n.90392426T> rs202105360 0.94414 intergenic_region ZNF37A :n.39556257C> NA 0.85186 intergenic_region OR52Z1 :n.5181851C>A rs11036137 0.85181 intergenic_region OR52Z1 :n.5181852C>T rs11036138 0.94791 intron_variant MGAT4C NM_013244.3:c rs10745426 0.94612 intergenic_region UQCRFS1 :n.27863467T> rs4805690 1000GP3_AF gnomAD_AF TOPMed_AF 0.95028 0.914138 0.918052 NA 0.000328515 NA NA 0.000588813 3.19E-05 NA 0.000588967 NA NA 0.000986388 NA NA 0.000163441 1.59E-05 NA 0.000293121 5.57E-05 0.0115815 0.0114781 0.0110777 NA 0.000130149 NA NA NA 0.496711 NA NA 0.495031 0.874401 0.857722 0.844913 NA 6.55E-05 NA NA NA 0.502317 0.699681 0.714272 0.702607 0.699681 0.714141 0.702512 0.869609 0.846502 0.846028 0.945088 0.962243 0.951938