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: rs1131692320
rs1131692320
1 1.000 0.120 17 50187103 missense variant C/T snv 0.700 0
dbSNP: rs121912905
rs121912905
2 0.925 0.120 7 94408806 missense variant G/T snv 0.700 0
dbSNP: rs121912907
rs121912907
2 0.925 0.120 7 94415263 missense variant G/T snv 0.700 0
dbSNP: rs1554396283
rs1554396283
1 1.000 0.120 7 94410926 missense variant G/T snv 0.700 0
dbSNP: rs1555574303
rs1555574303
7 0.790 0.240 17 50196172 missense variant C/G snv 0.700 0
dbSNP: rs1800250
rs1800250
1 1.000 0.120 7 94427801 missense variant A/C snv 0.700 0
dbSNP: rs267606742
rs267606742
1 1.000 0.120 7 94427628 missense variant G/A snv 0.700 0
dbSNP: rs66490707
rs66490707
7 0.790 0.240 17 50195231 splice donor variant C/G;T snv 0.700 0
dbSNP: rs66523073
rs66523073
2 0.925 0.120 17 50188777 missense variant C/T snv 0.700 0
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: rs66612022
rs66612022
9 0.763 0.240 7 94409768 missense variant G/A;T snv 0.700 0
dbSNP: rs66619856
rs66619856
3 0.882 0.120 7 94410278 missense variant G/A;T snv 0.700 0
dbSNP: rs67368147
rs67368147
2 0.925 0.120 17 50191805 missense variant C/A;T snv 0.700 0
dbSNP: rs67543427
rs67543427
8 0.776 0.240 7 94410457 missense variant G/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: rs67693970
rs67693970
3 0.882 0.120 17 50190099 missense variant C/G;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: rs72645320
rs72645320
1 1.000 0.120 17 50197053 missense variant C/T snv 0.700 0
dbSNP: rs72648326
rs72648326
7 0.790 0.240 17 50195288 stop gained G/A snv 0.700 0
dbSNP: rs72651642
rs72651642
7 0.790 0.240 17 50191826 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs72653131
rs72653131
3 0.882 0.120 17 50190045 missense variant C/T snv 0.700 0
dbSNP: rs72653170
rs72653170
10 0.752 0.240 17 50188908 missense variant G/A snv 8.0E-06 0.700 0
dbSNP: rs72654795
rs72654795
2 0.925 0.120 17 50188565 missense variant C/T snv 0.700 0
dbSNP: rs72656353
rs72656353
1 1.000 0.120 17 50185506 missense variant A/G snv 0.700 0