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: rs3218822
rs3218822
1 1.000 0.040 6 30912559 intron variant T/C snv 1.9E-02 0.700 1.000 1 2010 2010