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: rs113994095
rs113994095
31 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 0.010 1.000 1 2014 2014
dbSNP: rs761649878
rs761649878
2 0.925 0.080 15 89318738 missense variant G/C snv 1.2E-05 0.010 1.000 1 2014 2014