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: rs12682865
rs12682865
1 1.000 0.080 9 113979934 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4979311
rs4979311
1 1.000 0.080 9 113987250 intron variant G/C snv 0.27 0.700 1.000 1 2012 2012