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: rs1057519738
rs1057519738
7 0.821 0.143 17 39725079 missense variant G/A snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs1057519757
rs1057519757
5 0.878 0.107 5 68293310 missense variant G/A,C snp 0.700 1 2016 2016
dbSNP: rs1057519891
rs1057519891
5 0.846 0.143 12 56088557 missense variant G/A,T snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs1057519892
rs1057519892
5 0.846 0.143 12 56088558 missense variant A/T snp 0.700 1 2016 2016
dbSNP: rs1057519893
rs1057519893
7 0.821 0.143 12 56085070 missense variant G/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519895
rs1057519895
13 0.734 0.214 4 152328232 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519896
rs1057519896
11 0.744 0.286 4 152326136 missense variant C/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519931
rs1057519931
5 0.846 0.143 3 179199141 missense variant G/C 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: rs1057519943
rs1057519943
5 0.878 0.143 12 132676598 missense variant G/C,T snp 0.700 1 2016 2016
dbSNP: rs1057519944
rs1057519944
5 0.878 0.143 12 132676599 missense variant G/A 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: rs1057519981
rs1057519981
17 0.715 0.321 17 7674251 stop lost A/C,G snp 0.700 1 2016 2016
dbSNP: rs1057519982
rs1057519982
12 0.734 0.321 17 7674239 missense variant A/C,T snp 0.700 1 2016 2016
dbSNP: rs1057519989
rs1057519989
15 0.724 0.214 17 7674233 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519990
rs1057519990
18 0.699 0.321 17 7673824 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs1057519991
rs1057519991
19 0.692 0.214 17 7675076 missense variant T/A,C,G snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs1057519996
rs1057519996
15 0.724 0.321 17 7675217 splice acceptor variant T/A,C,G snp 0.700 1 2016 2016