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: rs7641603
rs7641603
1 1.000 0.080 3 21756848 intron variant C/A;T snv 0.700 1.000 1 2009 2009