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: rs8052139
rs8052139
1 1.000 0.080 16 31375541 intron variant C/A snv 0.28 0.700 1.000 1 2012 2012