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: rs114619974
rs114619974
1 1.000 0.080 4 105234376 missense variant G/A snv 5.2E-04 2.2E-03 0.700 0
dbSNP: rs116519313
rs116519313
1 1.000 0.080 4 105276128 missense variant T/C;G snv 1.3E-05 0.700 0
dbSNP: rs1283441077
rs1283441077
1 1.000 0.080 4 105276331 missense variant C/T snv 6.4E-06 0.700 0
dbSNP: rs1316795626
rs1316795626
1 1.000 0.080 4 105276287 missense variant G/A snv 6.4E-06 0.700 0
dbSNP: rs1406914931
rs1406914931
1 1.000 0.080 4 105276431 missense variant G/T snv 0.700 0
dbSNP: rs376570662
rs376570662
1 1.000 0.080 4 105235321 missense variant C/T snv 1.2E-04 1.7E-04 0.700 0
dbSNP: rs532738858
rs532738858
1 1.000 0.080 4 105236763 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs569067880
rs569067880
2 0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs749210253
rs749210253
1 1.000 0.080 4 105272630 missense variant G/A;T snv 3.8E-05; 6.4E-06 0.700 0
dbSNP: rs754215085
rs754215085
1 1.000 0.080 4 105276407 missense variant G/A snv 5.7E-05 1.4E-05 0.700 0
dbSNP: rs771761785
rs771761785
1 1.000 0.080 4 105243757 missense variant G/A;C snv 6.4E-06 0.700 0