Gene: ERCC6 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1198241866
rs1198241866
ERCC6 ; PGBD3
A 0.700 GeneticVariation CLINVAR Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells. 11809892

2002
dbSNP: rs1198241866
rs1198241866
ERCC6 ; PGBD3
A 0.700 GeneticVariation CLINVAR Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. 19894250

2010
dbSNP: rs1198472093
rs1198472093
ERCC6
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1198472093
rs1198472093
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1228919836
rs1228919836
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1254008304
rs1254008304
ERCC6 ; PGBD3
TGG 0.700 GeneticVariation CLINVAR

dbSNP: rs1287286877
rs1287286877
ERCC6
TTC 0.700 GeneticVariation CLINVAR Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. 19894250

2010
dbSNP: rs1317145066
rs1317145066
ERCC6
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1362935450
rs1362935450
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1386369933
rs1386369933
ERCC6
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs1441655600
rs1441655600
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554787554
rs1554787554
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554789393
rs1554789393
ERCC6
TT 0.700 GeneticVariation CLINVAR

dbSNP: rs1554793174
rs1554793174
ERCC6 ; PGBD3
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554793270
rs1554793270
ERCC6 ; PGBD3
A 0.700 GeneticVariation CLINVAR Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome. 19894250

2010
dbSNP: rs1554794073
rs1554794073
ERCC6
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554794360
rs1554794360
ERCC6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554794620
rs1554794620
ERCC6
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554794640
rs1554794640
ERCC6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554794641
rs1554794641
ERCC6
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1554873950
rs1554873950
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554873973
rs1554873973
ERCC6
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554874073
rs1554874073
ERCC6
T 0.700 GeneticVariation CLINVAR The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair. 26620705

2016
dbSNP: rs1554875114
rs1554875114
ERCC6
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554875154
rs1554875154
ERCC6
TA 0.700 GeneticVariation CLINVAR