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rs1805386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1805386(C;C)
Make rs1805386(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108209565
GeneLIG4
is asnp
is mentioned by
dbSNPrs1805386
ebirs1805386
HLIrs1805386
Exacrs1805386
Varsomers1805386
Maprs1805386
PheGenIrs1805386
hapmaprs1805386
1000 genomesrs1805386
hgdprs1805386
ensemblrs1805386
gopubmedrs1805386
geneviewrs1805386
scholarrs1805386
googlers1805386
pharmgkbrs1805386
gwascentralrs1805386
openSNPrs1805386
23andMers1805386
23andMe allrs1805386
SNP Nexus

SNPshotrs1805386
SNPdbers1805386
MSV3drs1805386
GWAS Ctlgrs1805386
GMAF0.09366
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 23075580] Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients


[PMID 23936089OA-icon.png] Polymorphisms in DNA-Repair Genes in a Cohort of Prostate Cancer Patients from Different Areas in Spain: Heterogeneity between Populations as a Confounding Factor in Association Studies


[PMID 19127255OA-icon.png] Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.


[PMID 20386703OA-icon.png] Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.


[PMID 21974800] DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome.


ClinVar
Risk rs1805386(C;C)
Alt rs1805386(C;C)
Reference rs1805386(T;T)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene LIG4
CLNDBN not specified
Reversed 1
HGVS NC_000013.10:g.108861913A>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000117489.2,