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: rs1555574303
rs1555574303
7 0.790 0.240 17 50196172 missense variant C/G 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: rs66555264
rs66555264
7 0.790 0.240 17 50192993 splice donor 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: rs72645357
rs72645357
8 0.776 0.240 17 50196163 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: rs72656354
rs72656354
1 1.000 0.160 7 94395818 intron variant A/G snv 0.700 0
dbSNP: rs72667019
rs72667019
1 1.000 0.160 17 50198506 splice acceptor variant T/A;C snv 0.700 0
dbSNP: rs72667020
rs72667020
1 1.000 0.160 17 50198505 splice acceptor variant C/A;G;T snv 0.700 0
dbSNP: rs72667022
rs72667022
1 1.000 0.160 17 50198433 missense variant C/T snv 0.700 0
dbSNP: rs797044459
rs797044459
1 1.000 0.160 7 94404567 frameshift variant -/C delins 0.700 0
dbSNP: rs74821926
rs74821926
ALB
1 1.000 0.160 4 73404398 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 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: rs67162110
rs67162110
1 1.000 0.160 7 94412122 splice donor variant G/A;C snv 1.2E-05 0.700 0
dbSNP: rs72659343
rs72659343
1 1.000 0.160 7 94428367 stop gained G/A;T snv 2.0E-05 0.700 0