BAP1, BRCA1 associated protein 1, 8314

N. diseases: 299; N. variants: 72
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060503726
rs1060503726
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060503727
rs1060503727
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060503731
rs1060503731
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060503732
rs1060503732
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1060503735
rs1060503735
Entrez Id: 8314;51533
Gene Symbol: BAP1;PHF7
BAP1;PHF7
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 CausalMutation CLINVAR
dbSNP: rs1060503743
rs1060503743
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs1060503744
rs1060503744
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060503750
rs1060503750
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1060503750
rs1060503750
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1064795638
rs1064795638
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1351986946
rs1351986946
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs143901408
rs143901408
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553644634
rs1553644634
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553644815
rs1553644815
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1553644815
rs1553644815
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1553644922
rs1553644922
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553644949
rs1553644949
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553645117
rs1553645117
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553645126
rs1553645126
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1553645136
rs1553645136
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
CT 0.700 CausalMutation CLINVAR
dbSNP: rs1553645146
rs1553645146
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553645164
rs1553645164
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553645329
rs1553645329
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553645492
rs1553645492
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
GT 0.700 CausalMutation CLINVAR
dbSNP: rs1553645497
rs1553645497
Entrez Id: 8314
Gene Symbol: BAP1
BAP1
CUI: C3280492
Disease:
TUMOR PREDISPOSITION SYNDROME
CT 0.700 CausalMutation CLINVAR