rs1805363
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1805363(A;A) |
Make rs1805363(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 94493786 |
Gene | ANKRD49, MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs1805363 |
dbSNP (classic) | rs1805363 |
ClinGen | rs1805363 |
ebi | rs1805363 |
HLI | rs1805363 |
Exac | rs1805363 |
Gnomad | rs1805363 |
Varsome | rs1805363 |
LitVar | rs1805363 |
Map | rs1805363 |
PheGenI | rs1805363 |
Biobank | rs1805363 |
1000 genomes | rs1805363 |
hgdp | rs1805363 |
ensembl | rs1805363 |
geneview | rs1805363 |
scholar | rs1805363 |
rs1805363 | |
pharmgkb | rs1805363 |
gwascentral | rs1805363 |
openSNP | rs1805363 |
23andMe | rs1805363 |
SNPshot | rs1805363 |
SNPdbe | rs1805363 |
MSV3d | rs1805363 |
GWAS Ctlg | rs1805363 |
GMAF | 0.03903 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24623370] Next-generation sequencing identifies germline MRE11A variants as markers of radiotherapy outcomes in muscle-invasive bladder cancer
ClinVar | |
---|---|
Risk | rs1805363(A;A) |
Alt | rs1805363(A;A) |
Reference | Rs1805363(G;G) |
Significance | Probable-non-pathogenic |
Disease | Ataxia-telangiectasia-like disorder 1 |
Variation | info |
Gene | ANKRD49 MRE11A |
CLNDBN | Ataxia-telangiectasia-like disorder 1 |
Reversed | 1 |
HGVS | NC_000011.9:g.94226952C>T |
CLNSRC | |
CLNACC | RCV000319622.1, |