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: rs121909350
rs121909350
1 1.000 0.080 20 35434282 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.800 1.000 3 2002 2008
dbSNP: rs121909351
rs121909351
1 1.000 0.080 20 35434109 missense variant G/T snv 0.800 1.000 3 2002 2008
dbSNP: rs28936683
rs28936683
3 0.882 0.080 20 35434093 missense variant A/G snv 7.0E-06 0.800 0
dbSNP: rs1553941890
rs1553941890
4 0.851 0.080 4 95129916 missense variant C/A snv 0.700 0