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rs1799801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1799801(C;C)
Make rs1799801(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position13948101
GeneERCC4
is asnp
is mentioned by
dbSNPrs1799801
ebirs1799801
HLIrs1799801
Exacrs1799801
Varsomers1799801
Maprs1799801
PheGenIrs1799801
hapmaprs1799801
1000 genomesrs1799801
hgdprs1799801
ensemblrs1799801
gopubmedrs1799801
geneviewrs1799801
scholarrs1799801
googlers1799801
pharmgkbrs1799801
gwascentralrs1799801
openSNPrs1799801
23andMers1799801
23andMe allrs1799801
SNP Nexus

SNPshotrs1799801
SNPdbers1799801
MSV3drs1799801
GWAS Ctlgrs1799801
GMAF0.2264
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21622940OA-icon.png] Single Nucleotide Polymorphisms in DNA Repair Genes and Association with Breast Cancer Risk in the WEB Study


[PMID 22768293OA-icon.png] Association between XPF Polymorphisms and Cancer Risk: A Meta-Analysis

[PMID 17299578OA-icon.png] Genetic polymorphisms in the nucleotide excision repair pathway and lung cancer risk: a meta-analysis.

[PMID 19706757OA-icon.png] Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer.


[PMID 24353636OA-icon.png] Effect of Xeroderma pigmentosum complementation group F polymorphisms and H.pylori infection on the risk of gastric cancer


ClinVar
Risk rs1799801(C;C)
Alt rs1799801(C;C)
Reference rs1799801(T;T)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene ERCC4
CLNDBN not specified
Reversed 0
HGVS NC_000016.9:g.14041958T>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000116988.2,