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: rs871657
rs871657
2 1.000 0.080 2 102154881 intron variant C/T snv 0.22 0.700 1.000 1 2011 2011