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: rs35874116
rs35874116
3 1.000 0.040 1 18854899 missense variant T/C snv 0.29 0.31 0.010 1.000 1 2015 2015
dbSNP: rs9701796
rs9701796
1 1.000 0.040 1 18859635 missense variant G/C snv 0.78 0.79 0.010 1.000 1 2015 2015