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rs2276465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2276465(A;A)
Make rs2276465(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position13949157
GeneERCC4
is asnp
is mentioned by
dbSNPrs2276465
dbSNP (old)rs2276465
ClinGenrs2276465
ebirs2276465
HLIrs2276465
Exacrs2276465
Varsomers2276465
Maprs2276465
PheGenIrs2276465
Biobankrs2276465
1000 genomesrs2276465
hgdprs2276465
ensemblrs2276465
gopubmedrs2276465
geneviewrs2276465
scholarrs2276465
googlers2276465
pharmgkbrs2276465
gwascentralrs2276465
openSNPrs2276465
23andMers2276465
23andMe allrs2276465
SNP Nexus

SNPshotrs2276465
SNPdbers2276465
MSV3drs2276465
GWAS Ctlgrs2276465
GMAF0.2649
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 23909490OA-icon.png] Polymorphisms in the ERCC1 and XPF Genes and Risk of Breast Cancer in a Chinese Population


[PMID 22848636OA-icon.png] Association between single nucleotide polymorphisms in ERCC4 and risk of squamous cell carcinoma of the head and neck.


ClinVar
Risk rs2276465(A;A)
Alt rs2276465(A;A)
Reference Rs2276465(G;G)
Significance Non-pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene ERCC4
CLNDBN Xeroderma pigmentosum
Reversed 0
HGVS NC_000016.9:g.14043014G>A
CLNSRC
CLNACC RCV000269593.1,