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rs238417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs238417(C;G)
Make rs238417(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position45353210
GeneERCC2
is asnp
is mentioned by
dbSNPrs238417
dbSNP (old)rs238417
ClinGenrs238417
ebirs238417
HLIrs238417
Exacrs238417
Gnomadrs238417
Varsomers238417
Maprs238417
PheGenIrs238417
Biobankrs238417
1000 genomesrs238417
hgdprs238417
ensemblrs238417
gopubmedrs238417
geneviewrs238417
scholarrs238417
googlers238417
pharmgkbrs238417
gwascentralrs238417
openSNPrs238417
23andMers238417
23andMe allrs238417
SNP Nexus

SNPshotrs238417
SNPdbers238417
MSV3drs238417
GWAS Ctlgrs238417
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 26967386OA-icon.png] The association of six polymorphisms of five genes involved in three steps of nucleotide excision repair pathways with hepatocellular cancer risk.


ClinVar
Risk rs238417(A;A) rs238417(G;G)
Alt rs238417(A;A) rs238417(G;G)
Reference Rs238417(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ERCC2
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.45856468G>C
CLNSRC
CLNACC RCV000253904.1,