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: rs587783309
rs587783309
ATP7B
1 1.000 0.160 13 51944164 missense variant G/A snv 7.0E-06 0.800 1.000 23 1995 2017
dbSNP: rs587783315
rs587783315
ATP7B
1 1.000 0.160 13 51941089 missense variant G/A;C snv 0.700 1.000 23 1995 2017
dbSNP: rs751798708
rs751798708
ATP7B
1 1.000 0.160 13 51958331 missense variant A/C snv 7.0E-06 0.800 1.000 23 1995 2017
dbSNP: rs780811477
rs780811477
ATP7B
1 1.000 0.160 13 51935599 missense variant A/C;G snv 0.700 1.000 23 1995 2017
dbSNP: rs786204643
rs786204643
ATP7B
1 1.000 0.160 13 51974966 missense variant C/A snv 7.0E-06 0.810 1.000 23 1995 2017
dbSNP: rs1169959260
rs1169959260
ATP7B
1 1.000 0.160 13 51949681 missense variant A/C snv 7.0E-06 0.700 1.000 20 1995 2015
dbSNP: rs1397083296
rs1397083296
ATP7B
1 1.000 0.160 13 51942518 missense variant A/G snv 7.0E-06 0.700 1.000 20 1995 2015
dbSNP: rs1414727042
rs1414727042
ATP7B
1 1.000 0.160 13 51946316 missense variant T/C snv 0.700 1.000 20 1995 2015
dbSNP: rs377144951
rs377144951
ATP7B
1 1.000 0.160 13 51937383 missense variant A/G snv 1.4E-05 0.700 1.000 20 1995 2015
dbSNP: rs768671894
rs768671894
ATP7B
1 1.000 0.160 13 51950328 missense variant G/A snv 7.0E-06 0.800 1.000 20 1995 2019
dbSNP: rs1057517310
rs1057517310
ATP7B
1 1.000 0.160 13 51949710 missense variant C/A snv 0.800 1.000 3 2007 2017
dbSNP: rs1365425480
rs1365425480
ATP7B
1 1.000 0.160 13 51935593 missense variant C/G snv 0.700 1.000 3 2008 2017
dbSNP: rs199623434
rs199623434
ATP7B
1 1.000 0.160 13 51946382 missense variant C/G snv 0.800 1.000 3 2005 2017
dbSNP: rs755851188
rs755851188
ATP7B
1 1.000 0.160 13 51946293 missense variant C/T snv 7.0E-06 0.700 1.000 3 2008 2017
dbSNP: rs1131691741
rs1131691741
ATP7B
1 1.000 0.160 13 51937305 missense variant T/G snv 7.0E-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: 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: rs193922107
rs193922107
ATP7B
1 1.000 0.160 13 51939091 missense variant G/A snv 4.0E-06 0.800 1.000 0 1996 2015
dbSNP: rs770533110
rs770533110
ATP7B
1 1.000 0.160 13 51958444 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs1387431334
rs1387431334
ATP7B
1 1.000 0.160 13 51941105 missense variant T/C snv 4.0E-06 7.0E-06 0.700 1.000 20 1995 2015
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: rs749380700
rs749380700
ATP7B
1 1.000 0.160 13 51937367 missense variant G/C snv 4.0E-06 0.700 0