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: rs9468925
rs9468925
1 0.851 0.040 6 31291060 intron variant G/A snv 0.44 0.820 1.000 1 2010 2012
dbSNP: rs10484554
rs10484554
8 0.807 0.200 6 31306778 intron variant C/T snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs2524123
rs2524123
5 0.925 0.040 6 31297537 intron variant T/C snv 0.34 0.700 1.000 1 2010 2010