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: rs185638763
rs185638763
4 0.882 0.120 3 38599001 missense variant G/A;T snv 1.2E-05 0.700 1.000 21 1998 2016
dbSNP: rs193922726
rs193922726
1 1.000 0.080 3 38551188 missense variant G/A;C snv 6.0E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473050
rs199473050
1 1.000 0.080 3 38633098 missense variant A/C snv 4.4E-05 1.4E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473051
rs199473051
2 0.925 0.120 3 38633058 missense variant C/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473052
rs199473052
1 1.000 0.080 3 38630425 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473053
rs199473053
1 1.000 0.080 3 38630422 missense variant A/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473054
rs199473054
1 1.000 0.080 3 38630420 missense variant C/G;T snv 2.0E-05; 2.8E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473055
rs199473055
3 0.882 0.120 3 38630393 missense variant G/A;C snv 4.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473056
rs199473056
1 1.000 0.080 3 38630376 missense variant G/A;T snv 3.6E-05; 4.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473058
rs199473058
2 0.925 0.080 3 38630341 missense variant C/T snv 4.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473062
rs199473062
5 0.827 0.120 3 38622401 stop gained C/A;G;T snv 4.1E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473063
rs199473063
1 1.000 0.080 3 38620929 missense variant C/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473065
rs199473065
1 1.000 0.080 3 38620921 missense variant G/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473066
rs199473066
1 1.000 0.080 3 38620910 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473067
rs199473067
1 1.000 0.080 3 38620900 missense variant G/A;T snv 1.6E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473070
rs199473070
2 0.925 0.120 3 38613811 missense variant A/G;T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473074
rs199473074
1 1.000 0.080 3 38613758 missense variant T/C snv 4.2E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473076
rs199473076
3 0.925 0.120 3 38609950 missense variant C/T snv 8.0E-06 2.8E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473079
rs199473079
2 1.000 0.080 3 38609860 missense variant G/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473081
rs199473081
1 1.000 0.080 3 38609841 missense variant A/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473088
rs199473088
1 1.000 0.080 3 38609770 missense variant C/T snv 4.0E-06 1.4E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473090
rs199473090
1 1.000 0.080 3 38608194 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.8E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473091
rs199473091
1 1.000 0.080 3 38608190 missense variant G/T snv 8.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473092
rs199473092
3 0.925 0.080 3 38608175 missense variant A/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473093
rs199473093
2 0.925 0.080 3 38606802 missense variant G/A snv 0.700 1.000 21 1998 2016