rs876660269
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs876660269(-;A) |
Make rs876660269(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 94445850 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs876660269 |
dbSNP (classic) | rs876660269 |
ClinGen | rs876660269 |
ebi | rs876660269 |
HLI | rs876660269 |
Exac | rs876660269 |
Gnomad | rs876660269 |
Varsome | rs876660269 |
LitVar | rs876660269 |
Map | rs876660269 |
PheGenI | rs876660269 |
Biobank | rs876660269 |
1000 genomes | rs876660269 |
hgdp | rs876660269 |
ensembl | rs876660269 |
geneview | rs876660269 |
scholar | rs876660269 |
rs876660269 | |
pharmgkb | rs876660269 |
gwascentral | rs876660269 |
openSNP | rs876660269 |
23andMe | rs876660269 |
SNPshot | rs876660269 |
SNPdbe | rs876660269 |
MSV3d | rs876660269 |
GWAS Ctlg | rs876660269 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876660269(A;A) |
Alt | rs876660269(A;A) |
Reference | Rs876660269(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94179017dupT |
CLNSRC | |
CLNACC | RCV000218130.1, |