Have questions? Visit https://www.reddit.com/r/SNPedia

rs2020955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2020955(C;C)
Make rs2020955(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position13944802
GeneERCC4
is asnp
is mentioned by
dbSNPrs2020955
ebirs2020955
HLIrs2020955
Exacrs2020955
Varsomers2020955
Maprs2020955
PheGenIrs2020955
hapmaprs2020955
1000 genomesrs2020955
hgdprs2020955
ensemblrs2020955
gopubmedrs2020955
geneviewrs2020955
scholarrs2020955
googlers2020955
pharmgkbrs2020955
gwascentralrs2020955
openSNPrs2020955
23andMers2020955
23andMe allrs2020955
SNP Nexus

SNPshotrs2020955
SNPdbers2020955
MSV3drs2020955
GWAS Ctlgrs2020955
GMAF0.04867
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22768293OA-icon.png] Association between XPF Polymorphisms and Cancer Risk: A Meta-Analysis

[PMID 16465622OA-icon.png] Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes.

[PMID 18544627OA-icon.png] Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk.

[PMID 18711149OA-icon.png] Case-control analysis of nucleotide excision repair pathway and the risk of renal cell carcinoma.

[PMID 19270000OA-icon.png] Genetic susceptibility to esophageal cancer: the role of the nucleotide excision repair pathway.


GET Evidence
ERCC4-S662P
aa_change Ser662Pro
aa_change_short S662P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0677635
summary



ClinVar
Risk rs2020955(C;C)
Alt rs2020955(C;C)
Reference rs2020955(T;T)
Significance Untested
Disease not specified
Variation info
Gene ERCC4
CLNDBN not specified
Reversed 0
HGVS NC_000016.9:g.14038659T>C
CLNSRC ClinVar
CLNACC RCV000120806.1,