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: rs72645365
rs72645365
2 0.925 0.120 17 50195656 missense variant C/A snv 0.700 1.000 11 1989 2007
dbSNP: rs72648353
rs72648353
1 1.000 17 50194384 missense variant C/A snv 0.700 1.000 11 1989 2007
dbSNP: rs67507747
rs67507747
5 0.827 0.160 17 50194032 missense variant C/A;G;T snv 0.700 1.000 11 1989 2007
dbSNP: rs66721653
rs66721653
1 1.000 17 50195665 missense variant C/A;T snv 0.800 1.000 12 1989 2015
dbSNP: rs72648322
rs72648322
1 1.000 17 50195330 missense variant C/A;T snv 0.800 1.000 12 1989 2015
dbSNP: rs1114167402
rs1114167402
2 0.925 0.120 17 50186507 missense variant C/A;T snv 4.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs67368147
rs67368147
2 0.925 0.120 17 50191805 missense variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs66527965
rs66527965
31 0.763 0.240 17 50193038 missense variant C/A;T snv 0.700 0
dbSNP: rs66555264
rs66555264
7 0.790 0.240 17 50192993 splice donor variant C/A;T snv 0.700 0
dbSNP: rs67182491
rs67182491
1 1.000 17 50195575 missense variant C/A;T snv 0.700 0
dbSNP: rs67682641
rs67682641
6 0.807 0.240 17 50194375 missense variant C/A;T snv 0.700 0
dbSNP: rs67879854
rs67879854
7 0.790 0.240 17 50190578 missense variant C/A;T snv 0.700 0
dbSNP: rs68114505
rs68114505
1 1.000 17 50191814 missense variant C/A;T snv 0.700 0
dbSNP: rs1555574303
rs1555574303
7 0.790 0.240 17 50196172 missense variant C/G snv 0.700 0
dbSNP: rs67693970
rs67693970
3 0.882 0.120 17 50190099 missense variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs72645328
rs72645328
3 0.882 0.120 17 50196670 missense variant C/G;T snv 0.010 1.000 1 2000 2000
dbSNP: rs66490707
rs66490707
7 0.790 0.240 17 50195231 splice donor variant C/G;T snv 0.700 0
dbSNP: rs66501246
rs66501246
2 0.925 0.120 17 50195441 missense variant C/G;T snv 0.700 0
dbSNP: rs67364703
rs67364703
1 1.000 17 50197948 splice donor variant C/G;T snv 0.700 0
dbSNP: rs72645321
rs72645321
2 0.925 0.120 17 50197045 missense variant C/T snv 0.700 1.000 11 1989 2007
dbSNP: rs72651636
rs72651636
1 1.000 17 50191868 missense variant C/T snv 0.700 1.000 11 1989 2007
dbSNP: rs72653169
rs72653169
1 1.000 17 50188920 missense variant C/T snv 0.800 1.000 11 1989 2007
dbSNP: rs121908672
rs121908672
3 0.925 0.080 11 68357802 missense variant C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs66523073
rs66523073
2 0.925 0.120 17 50188777 missense variant C/T snv 0.010 1.000 1 1994 1994
dbSNP: rs72645357
rs72645357
8 0.776 0.240 17 50196163 missense variant C/T snv 0.700 1.000 1 2015 2015