ATM, ATM serine/threonine kinase, 472

N. diseases: 684; N. variants: 974
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434221
rs121434221
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0334634
Disease:
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
G 0.800 CausalMutation CLINVAR
dbSNP: rs121434221
rs121434221
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0334634
Disease:
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
0.800 GeneticVariation UNIPROT
dbSNP: rs587781302
rs587781302
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
G 0.800 GeneticVariation CLINVAR
dbSNP: rs786202826
rs786202826
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
G 0.800 GeneticVariation CLINVAR
dbSNP: rs876659365
rs876659365
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
G 0.800 CausalMutation CLINVAR
dbSNP: rs28904921
rs28904921
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0006142
Disease:
Malignant neoplasm of breast
G 0.780 CausalMutation CLINVAR
dbSNP: rs587779852
rs587779852
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0006142
Disease:
Malignant neoplasm of breast
T 0.710 CausalMutation CLINVAR
dbSNP: rs1025339570
rs1025339570
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1049900772
rs1049900772
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057516229
rs1057516229
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516235
rs1057516235
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516238
rs1057516238
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516250
rs1057516250
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
GA 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516301
rs1057516301
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516358
rs1057516358
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
AC 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516393
rs1057516393
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
CT 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516393
rs1057516393
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
CT 0.700 CausalMutation CLINVAR
dbSNP: rs1057516446
rs1057516446
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516525
rs1057516525
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516540
rs1057516540
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516541
rs1057516541
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
TA 0.700 CausalMutation CLINVAR
dbSNP: rs1057516553
rs1057516553
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516590
rs1057516590
Entrez Id: 472
Gene Symbol: ATM
ATM
CUI: C0004135
Disease:
Ataxia Telangiectasia
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516599
rs1057516599
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057516599
rs1057516599
Entrez Id: 472;160140
Gene Symbol: ATM;C11orf65
ATM;C11orf65
CUI: C0004135
Disease:
Ataxia Telangiectasia
T 0.700 GeneticVariation CLINVAR