Gene: BIVM-ERCC5 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1047768
rs1047768
ERCC5 ; BIVM-ERCC5
0.010 GeneticVariation BEFREE We evaluated the associations between six single nucleotide polymorphisms (SNPs) in XPG (rs1047768 T>C, rs2296147 T>C, rs2227869 G>C, rs2094258 C>T, rs751402 C>T, and rs873601 G>A) and cancer risk. 28416771

2017
dbSNP: rs121434570
rs121434570
ERCC5 ; BIVM-ERCC5
T 0.700 CausalMutation CLINVAR

dbSNP: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress. 23255472

2013
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: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients. 12060391

2002
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: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy. 11228268

2001
dbSNP: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity. 11841555

2002
dbSNP: rs121434571
rs121434571
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. 10447254

1999
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: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients. 12060391

2002
dbSNP: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity. 11841555

2002
dbSNP: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress. 23255472

2013
dbSNP: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy. 11228268

2001
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: rs121434574
rs121434574
ERCC5 ; BIVM-ERCC5
0.700 GeneticVariation UNIPROT A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. 10447254

1999
dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
C 0.800 CausalMutation CLINVAR

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: 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: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy. 11228268

2001
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: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress. 23255472

2013
dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients. 12060391

2002
dbSNP: rs121434575
rs121434575
ERCC5 ; BIVM-ERCC5
0.800 GeneticVariation UNIPROT The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity. 11841555

2002
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