Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs62026376
rs62026376
2 0.925 0.120 16 11134855 intron variant C/T snv 0.18 0.710 1.000 1 2014 2014
dbSNP: rs35441874
rs35441874
3 0.882 0.120 16 11119164 intron variant T/A snv 0.19 0.700 1.000 2 2019 2019
dbSNP: rs7203459
rs7203459
2 1.000 0.080 16 11136846 intron variant T/C snv 0.23 0.700 1.000 2 2016 2019
dbSNP: rs11645657
rs11645657
2 1.000 0.080 16 11129597 intron variant C/A;G snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs12935657
rs12935657
2 0.925 0.080 16 11125184 intron variant G/A snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs17806299
rs17806299
1 1.000 0.080 16 11106123 intron variant G/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs36045143
rs36045143
3 1.000 0.080 16 11131109 intron variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs9923856
rs9923856
1 1.000 0.080 16 11116558 intron variant T/C snv 0.41 0.700 1.000 1 2017 2017