Gene: BIVM-ERCC5 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
C 0.800 CausalMutation CLINVAR

dbSNP: rs267607280
rs267607280
ERCC5 ; BIVM-ERCC5
C 0.800 CausalMutation CLINVAR

dbSNP: rs267607281
rs267607281
ERCC5 ; BIVM-ERCC5
A 0.800 CausalMutation CLINVAR

dbSNP: rs121434570
rs121434570
ERCC5 ; BIVM-ERCC5
T 0.700 CausalMutation CLINVAR

dbSNP: rs121434577
rs121434577
ERCC5 ; BIVM-ERCC5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1244074570
rs1244074570
ERCC5 ; BIVM-ERCC5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1244074570
rs1244074570
ERCC5 ; BIVM-ERCC5
T 0.700 GeneticVariation CLINVAR

dbSNP: rs752661599
rs752661599
ERCC5 ; BIVM-ERCC5
G 0.700 CausalMutation CLINVAR

dbSNP: rs786200919
rs786200919
ERCC5 ; BIVM-ERCC5
G 0.700 CausalMutation CLINVAR

dbSNP: rs786200920
rs786200920
ERCC5 ; BIVM-ERCC5
G 0.700 CausalMutation CLINVAR

dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. 7951246

1994
dbSNP: rs267607280
rs267607280
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. 7951246

1994
dbSNP: rs267607281
rs267607281
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. 7951246

1994
dbSNP: rs121434576
rs121434576
ERCC5 ; BIVM-ERCC5
0.710 GeneticVariation UNIPROT Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. 7951246

1994
dbSNP: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. 7951246

1994
dbSNP: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. 7951246

1994
dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. 9096355

1997
dbSNP: rs267607280
rs267607280
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. 9096355

1997
dbSNP: rs267607281
rs267607281
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. 9096355

1997
dbSNP: rs121434576
rs121434576
ERCC5 ; BIVM-ERCC5
0.710 GeneticVariation UNIPROT A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. 9096355

1997
dbSNP: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. 9096355

1997
dbSNP: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. 9096355

1997
dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. 10447254

1999
dbSNP: rs267607280
rs267607280
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. 10447254

1999
dbSNP: rs267607281
rs267607281
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. 10447254

1999