Source: ALL
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: rs786204547
rs786204547
ATP7B
1 1.000 0.160 13 51941081 missense variant C/G;T snv 8.0E-06 0.800 1.000 34 1995 2017
dbSNP: rs121907998
rs121907998
ATP7B
1 1.000 0.160 13 51961849 missense variant A/C snv 5.2E-04 4.0E-04 0.800 1.000 33 1995 2017
dbSNP: rs587783309
rs587783309
ATP7B
1 1.000 0.160 13 51944164 missense variant G/A snv 7.0E-06 0.800 1.000 33 1995 2017
dbSNP: rs1286080173
rs1286080173
ATP7B
2 0.925 0.160 13 51942551 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.800 1.000 32 1995 2017
dbSNP: rs1555286628
rs1555286628
ATP7B
1 1.000 0.160 13 51944266 missense variant G/A snv 0.800 1.000 32 1995 2017
dbSNP: rs768671894
rs768671894
ATP7B
1 1.000 0.160 13 51950328 missense variant G/A snv 7.0E-06 0.800 1.000 32 1995 2019
dbSNP: rs1555291147
rs1555291147
ATP7B
1 1.000 0.160 13 51958372 missense variant T/C snv 0.800 1.000 31 1995 2017
dbSNP: rs374094065
rs374094065
ATP7B
1 1.000 0.160 13 51944161 missense variant T/G snv 1.5E-04 9.1E-05 0.800 1.000 31 1995 2017
dbSNP: rs72552285
rs72552285
ATP7B
1 1.000 0.160 13 51961859 missense variant C/A;G;T snv 8.0E-06; 1.2E-05; 4.0E-06 0.800 1.000 30 1994 2017
dbSNP: rs778749563
rs778749563
ATP7B
1 1.000 0.160 13 51941211 missense variant C/A;G snv 1.6E-05 0.800 1.000 30 1995 2017
dbSNP: rs786204483
rs786204483
ATP7B
1 1.000 0.160 13 51942497 missense variant C/T snv 4.0E-06 0.800 1.000 30 1995 2017
dbSNP: rs1038582488
rs1038582488
ATP7B
1 1.000 0.160 13 51946405 missense variant C/T snv 4.0E-06 0.800 1.000 29 1995 2017
dbSNP: rs1555283916
rs1555283916
ATP7B
1 1.000 0.160 13 51937579 missense variant T/G snv 0.800 1.000 29 1995 2017
dbSNP: rs371840514
rs371840514
ATP7B
1 1.000 0.160 13 51946291 missense variant G/A;T snv 5.8E-05 0.800 1.000 29 1995 2017
dbSNP: rs568009639
rs568009639
ATP7B
1 1.000 0.160 13 51939056 missense variant T/G snv 4.0E-06 2.1E-05 0.800 1.000 29 1995 2017
dbSNP: rs1057520235
rs1057520235
ATP7B
1 1.000 0.160 13 51950277 missense variant A/G snv 0.800 1.000 28 1995 2017
dbSNP: rs1213481140
rs1213481140
ATP7B
1 1.000 0.160 13 51941201 missense variant C/T snv 8.0E-06 0.800 1.000 28 1995 2017
dbSNP: rs121907996
rs121907996
ATP7B
1 1.000 0.160 13 51946438 missense variant C/T snv 3.6E-05 5.6E-05 0.800 1.000 28 1995 2017
dbSNP: rs121907997
rs121907997
ATP7B
1 1.000 0.160 13 51958369 missense variant G/A;C snv 3.6E-05; 4.0E-06 0.800 1.000 28 1995 2017
dbSNP: rs28942075
rs28942075
ATP7B
1 1.000 0.160 13 51958373 missense variant C/G;T snv 4.0E-06 0.800 1.000 28 1995 2017
dbSNP: rs540935874
rs540935874
ATP7B
1 1.000 0.160 13 51949775 missense variant C/G;T snv 0.800 1.000 28 1995 2017
dbSNP: rs587783299
rs587783299
ATP7B
1 1.000 0.160 13 51961906 missense variant C/G snv 8.8E-05 6.3E-05 0.800 1.000 28 1995 2016
dbSNP: rs755554442
rs755554442
ATP7B
1 1.000 0.160 13 51941186 missense variant G/A;C snv 5.6E-05 3.5E-05 0.800 1.000 28 1995 2017
dbSNP: rs786204718
rs786204718
ATP7B
1 1.000 0.160 13 51950069 missense variant C/T snv 1.6E-05 2.8E-05 0.800 1.000 28 1995 2017
dbSNP: rs121907992
rs121907992
ATP7B
1 1.000 0.160 13 51937583 missense variant C/T snv 2.8E-05 5.6E-05 0.800 1.000 27 1995 2017