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: rs9272346
rs9272346
6 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.810 1.000 1 2012 2019
dbSNP: rs17843604
rs17843604
2 0.925 0.120 6 32652506 intergenic variant C/T snv 0.49 0.800 1.000 1 2010 2019
dbSNP: rs2187668
rs2187668
10 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 1 2011 2011