Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434221
rs121434221
ATM ; C11orf65
CUI: C0334634
Disease: Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse 		0.800 GeneticVariation UNIPROT

dbSNP: rs879254065
rs879254065
ATM ; C11orf65
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 GeneticVariation UNIPROT

dbSNP: rs879254046
rs879254046
ATM
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 GeneticVariation UNIPROT

dbSNP: rs876658517
rs876658517
ATM ; C11orf65
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs866290641
rs866290641
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.700 GeneticVariation UNIPROT

dbSNP: rs745775382
rs745775382
ATM ; C11orf65
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 GeneticVariation UNIPROT

dbSNP: rs730881315
rs730881315
ATM ; C11orf65
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 GeneticVariation UNIPROT

dbSNP: rs587782310
rs587782310
ATM ; C11orf65
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 GeneticVariation UNIPROT

dbSNP: rs587782274
rs587782274
ATM ; C11orf65
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs587781894
rs587781894
ATM ; C11orf65
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 GeneticVariation UNIPROT

dbSNP: rs587779858
rs587779858
ATM
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 GeneticVariation UNIPROT

dbSNP: rs567060474
rs567060474
ATM ; C11orf65
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 GeneticVariation UNIPROT

dbSNP: rs371713984
rs371713984
ATM
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 GeneticVariation UNIPROT

dbSNP: rs369203092
rs369203092
ATM
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 GeneticVariation UNIPROT

dbSNP: rs202160435
rs202160435
ATM
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 GeneticVariation UNIPROT

dbSNP: rs138398778
rs138398778
ATM
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 GeneticVariation UNIPROT

dbSNP: rs1137889
rs1137889
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.700 GeneticVariation UNIPROT

dbSNP: rs11212587
rs11212587
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.700 GeneticVariation UNIPROT

dbSNP: rs1064795467
rs1064795467
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.700 GeneticVariation UNIPROT

dbSNP: rs587782292
rs587782292
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.810 GeneticVariation UNIPROT A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. 9521587

1998
dbSNP: rs876659365
rs876659365
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.800 GeneticVariation UNIPROT A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. 9521587

1998
dbSNP: rs786203054
rs786203054
ATM
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.800 GeneticVariation UNIPROT A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. 9521587

1998
dbSNP: rs786202826
rs786202826
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.800 GeneticVariation UNIPROT A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. 9521587

1998
dbSNP: rs587782202
rs587782202
ATM ; C11orf65
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.800 GeneticVariation UNIPROT A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. 9521587

1998
dbSNP: rs587781511
rs587781511
ATM
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		0.800 GeneticVariation UNIPROT A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. 9521587

1998