Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786202760
rs786202760
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		T 0.800 CausalMutation CLINVAR

dbSNP: rs786202760
rs786202760
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		G 0.800 GeneticVariation CLINVAR

dbSNP: rs137852986
rs137852986
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		A 0.710 CausalMutation CLINVAR

dbSNP: rs878855159
rs878855159
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		CA 0.700 CausalMutation CLINVAR

dbSNP: rs878855151
rs878855151
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs878855151
rs878855151
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs878855151
rs878855151
BRIP1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR

dbSNP: rs878855151
rs878855151
BRIP1
CUI: C4016951
Disease: BREAST CANCER, EARLY-ONSET
BREAST CANCER, EARLY-ONSET 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs878855145
rs878855145
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		C 0.700 CausalMutation CLINVAR

dbSNP: rs878855145
rs878855145
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		C 0.700 CausalMutation CLINVAR

dbSNP: rs878855143
rs878855143
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs878855143
rs878855143
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs878855143
rs878855143
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs878855143
rs878855143
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs878855140
rs878855140
BRIP1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		GGTTGTTGAAATATCAATTTGATATA 0.700 CausalMutation CLINVAR

dbSNP: rs878855140
rs878855140
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		GGTTGTTGAAATATCAATTTGATATA 0.700 CausalMutation CLINVAR

dbSNP: rs878855140
rs878855140
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		GGTTGTTGAAATATCAATTTGATATA 0.700 CausalMutation CLINVAR

dbSNP: rs878855134
rs878855134
BRIP1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		AAG 0.700 CausalMutation CLINVAR

dbSNP: rs878855134
rs878855134
BRIP1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		AAG 0.700 CausalMutation CLINVAR

dbSNP: rs878855134
rs878855134
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		AAG 0.700 CausalMutation CLINVAR

dbSNP: rs876660937
rs876660937
BRIP1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs876660769
rs876660769
BRIP1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR

dbSNP: rs876660769
rs876660769
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		C 0.700 CausalMutation CLINVAR

dbSNP: rs876660613
rs876660613
BRIP1
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		T 0.700 CausalMutation CLINVAR

dbSNP: rs876660613
rs876660613
BRIP1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR