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: rs10974438
rs10974438
3 0.925 0.120 9 4291928 intron variant A/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1983753
rs1983753
1 9 4160364 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6415788
rs6415788
4 9 4118111 missense variant G/T snv 0.67 0.62 0.700 1.000 1 2017 2017