Gene: ERCC6 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202080674
rs202080674
ERCC6
A 0.800 CausalMutation CLINVAR

dbSNP: rs368728467
rs368728467
ERCC6
G 0.800 CausalMutation CLINVAR

dbSNP: rs368728467
rs368728467
ERCC6
T 0.800 CausalMutation CLINVAR

dbSNP: rs751292948
rs751292948
ERCC6
T 0.800 CausalMutation CLINVAR

dbSNP: rs1198472093
rs1198472093
ERCC6
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1198472093
rs1198472093
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121917900
rs121917900
ERCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs121917901
rs121917901
ERCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs121917903
rs121917903
ERCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs1228919836
rs1228919836
ERCC6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1254008304
rs1254008304
ERCC6 ; PGBD3
TGG 0.700 GeneticVariation CLINVAR

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: 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