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: 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: 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: rs181250704
rs181250704
ATP7B
1 1.000 0.160 13 51935019 missense variant G/A snv 1.1E-03 1.5E-03 0.700 1.000 23 1995 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: rs780811477
rs780811477
ATP7B
1 1.000 0.160 13 51935599 missense variant A/C;G snv 0.700 1.000 23 1995 2017
dbSNP: rs1555282678
rs1555282678
ATP7B
1 1.000 0.160 13 51935611 missense variant G/A snv 0.700 1.000 23 1995 2017
dbSNP: rs749171049
rs749171049
ATP7B
1 1.000 0.160 13 51935614 missense variant A/G snv 8.1E-06 0.700 0
dbSNP: rs776848753
rs776848753
ATP7B
1 1.000 0.160 13 51935629 missense variant G/A;C snv 4.0E-06 0.800 1.000 23 1995 2017
dbSNP: rs759551693
rs759551693
ATP7B
1 1.000 0.160 13 51935640 missense variant C/A;G snv 8.1E-06; 4.0E-06 0.700 1.000 20 1995 2015
dbSNP: rs1555282751
rs1555282751
ATP7B
1 1.000 0.160 13 51935654 missense variant C/T snv 0.700 1.000 23 1995 2017
dbSNP: rs1160679283
rs1160679283
ATP7B
1 1.000 0.160 13 51935660 missense variant A/G snv 4.1E-06 0.700 0
dbSNP: rs1388795855
rs1388795855
ATP7B
1 1.000 0.160 13 51935663 missense variant G/A snv 4.1E-06 0.700 1.000 20 1995 2015
dbSNP: rs587783318
rs587783318
ATP7B
1 1.000 0.160 13 51935678 missense variant C/T snv 1.2E-04 4.2E-05 0.800 1.000 23 1995 2017
dbSNP: rs779494870
rs779494870
ATP7B
1 1.000 0.160 13 51935695 missense variant C/T snv 1.3E-05 1.4E-05 0.700 0
dbSNP: rs587783317
rs587783317
ATP7B
1 1.000 0.160 13 51937276 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 23 1995 2017
dbSNP: rs1131691741
rs1131691741
ATP7B
1 1.000 0.160 13 51937305 missense variant T/G snv 7.0E-06 0.700 0
dbSNP: rs1333619338
rs1333619338
ATP7B
1 1.000 0.160 13 51937315 missense variant C/T snv 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: rs749380700
rs749380700
ATP7B
1 1.000 0.160 13 51937367 missense variant G/C snv 4.0E-06 0.700 0
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: rs753044473
rs753044473
ATP7B
1 1.000 0.160 13 51937487 missense variant C/T snv 2.4E-05 1.4E-05 0.700 1.000 20 1995 2015
dbSNP: rs199821556
rs199821556
ATP7B
1 1.000 0.160 13 51937493 missense variant C/T snv 2.0E-04 1.5E-04 0.800 1.000 23 1995 2017
dbSNP: rs1340942427
rs1340942427
ATP7B
1 1.000 0.160 13 51937495 missense variant G/T snv 0.700 0
dbSNP: rs776300396
rs776300396
ATP7B
1 1.000 0.160 13 51937502 missense variant C/T snv 2.0E-05 7.0E-06 0.700 1.000 23 1995 2017
dbSNP: rs373748155
rs373748155
ATP7B
1 1.000 0.160 13 51937516 missense variant G/A;C snv 8.0E-06 1.4E-05 0.700 1.000 23 1995 2017