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: rs185077999
rs185077999
2 0.925 0.160 8 105801293 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs767216159
rs767216159
2 0.925 0.160 14 53950809 missense variant G/A;C snv 1.2E-04; 1.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs768314738
rs768314738
2 0.925 0.160 X 85265151 missense variant C/T snv 1.1E-05 9.6E-06 0.010 1.000 1 2009 2009