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: rs3936215
rs3936215
1 1.000 0.080 9 16816757 intron variant C/T snv 0.37 0.700 1.000 1 2014 2014