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: rs13045986
rs13045986
1 1.000 0.080 21 31474270 intron variant G/A;C snv 0.700 1.000 1 2009 2009