RB1, RB transcriptional corepressor 1, 5925

N. diseases: 339; N. variants: 239
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434309
rs121434309
Entrez Id: 5925;10161
Gene Symbol: RB1;LPAR6
RB1;LPAR6
CUI: C3279470
Disease:
HYPOTRICHOSIS 8
T 0.800 CausalMutation CLINVAR
dbSNP: rs137853292
rs137853292
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
T 0.800 CausalMutation CLINVAR
dbSNP: rs137853296
rs137853296
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
C 0.800 CausalMutation CLINVAR
dbSNP: rs879255262
rs879255262
Entrez Id: 5925;10161
Gene Symbol: RB1;LPAR6
RB1;LPAR6
CUI: C3279470
Disease:
HYPOTRICHOSIS 8
A 0.800 CausalMutation CLINVAR
dbSNP: rs137853297
rs137853297
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
A 0.710 CausalMutation CLINVAR
dbSNP: rs483352690
rs483352690
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
C 0.710 CausalMutation CLINVAR
dbSNP: rs1050717570
rs1050717570
Entrez Id: 5925;112268118
Gene Symbol: RB1;LOC112268118
RB1;LOC112268118
CUI: C0035335
Disease:
Retinoblastoma
0.700 GeneticVariation UNIPROT
dbSNP: rs1060503067
rs1060503067
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060503074
rs1060503074
Entrez Id: 5925;112268118
Gene Symbol: RB1;LOC112268118
RB1;LOC112268118
CUI: C0035335
Disease:
Retinoblastoma
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1060503075
rs1060503075
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060503077
rs1060503077
Entrez Id: 5925;112268118
Gene Symbol: RB1;LOC112268118
RB1;LOC112268118
CUI: C0035335
Disease:
Retinoblastoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs1060503079
rs1060503079
Entrez Id: 5925;112268118
Gene Symbol: RB1;LOC112268118
RB1;LOC112268118
CUI: C0035335
Disease:
Retinoblastoma
A 0.700 CausalMutation CLINVAR
dbSNP: rs1060503087
rs1060503087
Entrez Id: 5925;112268118
Gene Symbol: RB1;LOC112268118
RB1;LOC112268118
CUI: C0035335
Disease:
Retinoblastoma
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1060503088
rs1060503088
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
G 0.700 CausalMutation CLINVAR
dbSNP: rs1064792974
rs1064792974
Entrez Id: 5925;100862704
Gene Symbol: RB1;RB1-DT
RB1;RB1-DT
CUI: C0035335
Disease:
Retinoblastoma
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690842
rs1131690842
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690842
rs1131690842
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
C 0.700 CausalMutation CLINVAR
dbSNP: rs1131690843
rs1131690843
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0035335
Disease:
Retinoblastoma
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1131690843
rs1131690843
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1131690844
rs1131690844
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690845
rs1131690845
Entrez Id: 5925;100862704
Gene Symbol: RB1;RB1-DT
RB1;RB1-DT
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
GG 0.700 CausalMutation CLINVAR
dbSNP: rs1131690847
rs1131690847
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690849
rs1131690849
Entrez Id: 5925
Gene Symbol: RB1
RB1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 CausalMutation CLINVAR
dbSNP: rs1131690851
rs1131690851
Entrez Id: 5925;112268118
Gene Symbol: RB1;LOC112268118
RB1;LOC112268118
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131690852
rs1131690852
Entrez Id: 5925;100862704
Gene Symbol: RB1;RB1-DT
RB1;RB1-DT
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
AC 0.700 CausalMutation CLINVAR