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: rs3131296
rs3131296
6 0.807 0.320 6 32205216 intron variant C/T snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs3134942
rs3134942
6 0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 0.700 1.000 1 2010 2010