Gene: ATP7B ×
Source: UNIPROT ×
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: rs1052485948
rs1052485948
ATP7B
1 1.000 0.160 13 51949764 missense variant A/C;G;T snv 4.0E-06; 8.0E-06 0.700 0
dbSNP: rs1131691741
rs1131691741
ATP7B
1 1.000 0.160 13 51937305 missense variant T/G snv 7.0E-06 0.700 0
dbSNP: rs1160679283
rs1160679283
ATP7B
1 1.000 0.160 13 51935660 missense variant A/G snv 4.1E-06 0.700 0
dbSNP: rs1173050016
rs1173050016
ATP7B
1 1.000 0.160 13 51964924 missense variant A/C snv 0.700 0
dbSNP: rs1230241288
rs1230241288
ATP7B
1 1.000 0.160 13 51949765 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs1314712150
rs1314712150
ATP7B
1 1.000 0.160 13 51937577 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1318758433
rs1318758433
ATP7B
1 1.000 0.160 13 51941110 missense variant C/T snv 8.0E-06 0.700 0
dbSNP: rs1330620114
rs1330620114
ATP7B
1 1.000 0.160 13 51941178 missense variant C/A snv 0.700 0
dbSNP: rs1333619338
rs1333619338
ATP7B
1 1.000 0.160 13 51937315 missense variant C/T snv 0.700 0
dbSNP: rs1340942427
rs1340942427
ATP7B
1 1.000 0.160 13 51937495 missense variant G/T snv 0.700 0
dbSNP: rs1362773192
rs1362773192
ATP7B
1 1.000 0.160 13 51958432 missense variant A/G snv 4.0E-06 0.700 0
dbSNP: rs182659444
rs182659444
ATP7B
1 1.000 0.160 13 51942466 missense variant C/T snv 1.8E-04 4.9E-05 0.700 0
dbSNP: rs374172791
rs374172791
ATP7B
1 1.000 0.160 13 51964895 missense variant G/A snv 1.6E-05 1.4E-05 0.700 0
dbSNP: rs375692175
rs375692175
ATP7B
1 1.000 0.160 13 51934859 missense variant G/A snv 1.2E-05 1.4E-05 0.700 0
dbSNP: rs377297166
rs377297166
ATP7B
1 1.000 0.160 13 51941185 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.700 0
dbSNP: rs41292782
rs41292782
ATP7B
1 1.000 0.160 13 51946372 missense variant G/A snv 1.2E-03 1.5E-03 0.800 0
dbSNP: rs551275663
rs551275663
ATP7B
1 1.000 0.160 13 51974750 missense variant C/A snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs59959366
rs59959366
ATP7B
1 1.000 0.160 13 51944239 missense variant C/G;T snv 8.0E-06 0.700 0
dbSNP: rs60003608
rs60003608
ATP7B
1 1.000 0.160 13 51946445 stop lost T/A;C snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs60986317
rs60986317
ATP7B
1 1.000 0.160 13 51934853 missense variant G/A snv 2.0E-03 2.8E-03 0.700 0
dbSNP: rs749171049
rs749171049
ATP7B
1 1.000 0.160 13 51935614 missense variant A/G snv 8.1E-06 0.700 0
dbSNP: rs749380700
rs749380700
ATP7B
1 1.000 0.160 13 51937367 missense variant G/C snv 4.0E-06 0.700 0
dbSNP: rs753330854
rs753330854
ATP7B
1 1.000 0.160 13 51937332 missense variant C/G;T snv 4.0E-06; 1.2E-04 0.700 0
dbSNP: rs765667658
rs765667658
ATP7B
1 1.000 0.160 13 51958505 missense variant A/G snv 4.0E-06 0.700 0
dbSNP: rs770340441
rs770340441
ATP7B
1 1.000 0.160 13 51946432 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.700 0