rs372000848
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs372000848(A;A) |
Make rs372000848(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 94470575 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs372000848 |
dbSNP (classic) | rs372000848 |
ClinGen | rs372000848 |
ebi | rs372000848 |
HLI | rs372000848 |
Exac | rs372000848 |
Gnomad | rs372000848 |
Varsome | rs372000848 |
LitVar | rs372000848 |
Map | rs372000848 |
PheGenI | rs372000848 |
Biobank | rs372000848 |
1000 genomes | rs372000848 |
hgdp | rs372000848 |
ensembl | rs372000848 |
geneview | rs372000848 |
scholar | rs372000848 |
rs372000848 | |
pharmgkb | rs372000848 |
gwascentral | rs372000848 |
openSNP | rs372000848 |
23andMe | rs372000848 |
SNPshot | rs372000848 |
SNPdbe | rs372000848 |
MSV3d | rs372000848 |
GWAS Ctlg | rs372000848 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs372000848(A;A) |
Alt | rs372000848(A;A) |
Reference | Rs372000848(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.94203741G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000115925.10, RCV000212563.1, |