rs10131
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | ||
(A;G) | ||
(G;G) | 0 | common in clinvar |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 108207498 |
Gene | LIG4 |
is a | snp |
is | mentioned by |
dbSNP | rs10131 |
dbSNP (classic) | rs10131 |
ClinGen | rs10131 |
ebi | rs10131 |
HLI | rs10131 |
Exac | rs10131 |
Gnomad | rs10131 |
Varsome | rs10131 |
LitVar | rs10131 |
Map | rs10131 |
PheGenI | rs10131 |
Biobank | rs10131 |
1000 genomes | rs10131 |
hgdp | rs10131 |
ensembl | rs10131 |
geneview | rs10131 |
scholar | rs10131 |
rs10131 | |
pharmgkb | rs10131 |
gwascentral | rs10131 |
openSNP | rs10131 |
23andMe | rs10131 |
SNPshot | rs10131 |
SNPdbe | rs10131 |
MSV3d | rs10131 |
GWAS Ctlg | rs10131 |
GMAF | 0.1143 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20386703]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, |