rs1805386

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs1805386(C;C)

Make rs1805386(C;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

108209565

Gene

LIG4

is a	snp
is	mentioned by
dbSNP	rs1805386
dbSNP (classic)	rs1805386
ClinGen	rs1805386
ebi	rs1805386
HLI	rs1805386
Exac	rs1805386
Gnomad	rs1805386
Varsome	rs1805386
LitVar	rs1805386
Map	rs1805386
PheGenI	rs1805386
Biobank	rs1805386
1000 genomes	rs1805386
hgdp	rs1805386
ensembl	rs1805386
geneview	rs1805386
scholar	rs1805386
google	rs1805386
pharmgkb	rs1805386
gwascentral	rs1805386
openSNP	rs1805386
23andMe	rs1805386
SNPshot	rs1805386
SNPdbe	rs1805386
MSV3d	rs1805386
GWAS Ctlg	rs1805386

GMAF

0.09366

Max Magnitude

0

?

(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 23936089 ] 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 19127255 ] Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.

[PMID 20386703 ] 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	Other
Disease	not specified Severe combined immunodeficiency with sensitivity to ionizing radiation Lig4 syndrome
Variation	info
Gene	LIG4
CLNDBN	not specified Severe combined immunodeficiency with sensitivity to ionizing radiation Lig4 syndrome
Reversed	1
HGVS	NC_000013.10:g.108861913A>G
CLNSRC	ClinVar University of Chicago
CLNACC	RCV000117489.2, RCV000270912.1, RCV000363160.1,