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: rs104886003
rs104886003
52 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs104894229
rs104894229
31 0.634 0.500 11 534289 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs104894230
rs104894230
42 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519862
rs1057519862
6 0.846 0.143 17 39723405 missense variant G/A snp 0.700 1 2016 2016
dbSNP: rs1057519883
rs1057519883
11 0.744 0.250 9 21971120 missense variant C/G,T snp 3.2E-05 0.700 1 2016 2016
dbSNP: rs1057519886
rs1057519886
11 0.744 0.250 3 41224609 missense variant T/A,C,G snp 0.700 1 2016 2016
dbSNP: rs1057519909
rs1057519909
6 0.801 0.250 15 66435116 missense variant A/C snp 0.700 1 2016 2016
dbSNP: rs1057519912
rs1057519912
5 0.846 0.179 X 71129408 missense variant C/G,T snp 0.700 1 2016 2016
dbSNP: rs1057519927
rs1057519927
16 0.724 0.179 3 179218295 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519932
rs1057519932
21 0.679 0.286 3 179234298 missense variant T/G snp 0.700 1 2016 2016
dbSNP: rs1057519938
rs1057519938
10 0.769 0.179 3 179203764 missense variant A/C,T snp 0.700 1 2016 2016
dbSNP: rs1057519939
rs1057519939
10 0.769 0.179 3 179203763 missense variant A/C snp 0.700 1 2016 2016
dbSNP: rs1057519940
rs1057519940
12 0.756 0.179 3 179218308 missense variant G/T snp 0.700 1 2016 2016
dbSNP: rs1057519946
rs1057519946
9 0.784 0.179 19 52212729 missense variant C/G,T snp 0.700 1 2016 2016
dbSNP: rs1057519947
rs1057519947
9 0.784 0.179 19 52212730 missense variant G/A snp 0.700 1 2016 2016
dbSNP: rs1057519956
rs1057519956
5 0.821 0.179 2 218583025 missense variant T/C snp 0.700 1 2016 2016
dbSNP: rs1057519957
rs1057519957
5 0.821 0.179 2 218583026 missense variant C/G snp 0.700 1 2016 2016
dbSNP: rs1057519962
rs1057519962
6 0.821 0.179 18 51067035 missense variant G/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519964
rs1057519964
1 1.000 0.071 17 49619282 missense variant A/C snp 0.700 1 2016 2016
dbSNP: rs1057519965
rs1057519965
1 1.000 0.071 17 49619280 missense variant G/A,C snp 8.0E-06 0.700 1 2016 2016
dbSNP: rs1057519966
rs1057519966
1 1.000 0.071 17 49619064 missense variant A/C,T snp 0.700 1 2016 2016
dbSNP: rs1057519967
rs1057519967
1 1.000 0.071 17 49619063 missense variant A/C,G snp 0.700 1 2016 2016
dbSNP: rs1057519968
rs1057519968
2 0.923 0.107 17 49619070 missense variant A/C,T snp 0.700 1 2016 2016
dbSNP: rs1057519969
rs1057519969
2 0.923 0.107 17 49619069 missense variant C/G snp 0.700 1 2016 2016
dbSNP: rs1057519970
rs1057519970
2 0.923 0.107 17 49619068 missense variant C/A snp 0.700 1 2016 2016