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: rs1190356035
rs1190356035
4 0.882 0.360 2 170853979 missense variant G/A snv 7.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs1309408215
rs1309408215
1 1.000 0.320 4 6301423 missense variant T/G snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs145639028
rs145639028
2 0.925 0.320 4 6289047 missense variant G/A snv 2.2E-05 1.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs1801208
rs1801208
4 0.882 0.360 4 6301162 missense variant G/A snv 5.7E-02 5.0E-02 0.010 1.000 1 2000 2000
dbSNP: rs1801275
rs1801275
58 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 0.010 1.000 1 2012 2012
dbSNP: rs199946797
rs199946797
3 0.882 0.360 4 6301467 missense variant C/A;T snv 6.7E-04 0.010 1.000 1 2012 2012
dbSNP: rs886044563
rs886044563
1 1.000 0.320 4 6300732 missense variant C/T snv 0.010 1.000 1 2005 2005