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

rs10131

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A)
(A;G)
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome13
Position108207498
GeneLIG4
is asnp
is mentioned by
dbSNPrs10131
dbSNP (old)rs10131
ClinGenrs10131
ebirs10131
HLIrs10131
Exacrs10131
Gnomadrs10131
Varsomers10131
Maprs10131
PheGenIrs10131
Biobankrs10131
1000 genomesrs10131
hgdprs10131
ensemblrs10131
gopubmedrs10131
geneviewrs10131
scholarrs10131
googlers10131
pharmgkbrs10131
gwascentralrs10131
openSNPrs10131
23andMers10131
23andMe allrs10131
SNP Nexus

SNPshotrs10131
SNPdbers10131
MSV3drs10131
GWAS Ctlgrs10131
GMAF0.1143
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20386703OA-icon.png]Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer PMC2851649


[PMID 27508978] Genetic effects of XRCC4 and ligase IV genes on human glioma.


ClinVar
Risk Rs10131(A;A)
Alt Rs10131(A;A)
Reference Rs10131(G;G)
Significance Probable-non-pathogenic
Disease Lig4 syndrome Severe combined immunodeficiency with sensitivity to ionizing radiation
Variation info
Gene LIG4
CLNDBN Lig4 syndrome Severe combined immunodeficiency with sensitivity to ionizing radiation
Reversed 1
HGVS NC_000013.10:g.108859846C>T
CLNSRC
CLNACC RCV000299250.1, RCV000393586.1,