Source: GWASDB ×
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: rs10968576
rs10968576
3 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.810 1.000 1 2012 2013
dbSNP: rs1412239
rs1412239
1 0.925 0.120 9 28425517 intron variant C/G snv 0.26 0.810 1.000 1 2013 2019
dbSNP: rs374068319
rs374068319
1 1.000 0.080 9 28425518 intron variant G/- del 0.700 1.000 1 2013 2013