rs779269083
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs779269083(A;A) |
Make rs779269083(A;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 94486009 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs779269083 |
dbSNP (classic) | rs779269083 |
ClinGen | rs779269083 |
ebi | rs779269083 |
HLI | rs779269083 |
Exac | rs779269083 |
Gnomad | rs779269083 |
Varsome | rs779269083 |
LitVar | rs779269083 |
Map | rs779269083 |
PheGenI | rs779269083 |
Biobank | rs779269083 |
1000 genomes | rs779269083 |
hgdp | rs779269083 |
ensembl | rs779269083 |
geneview | rs779269083 |
scholar | rs779269083 |
rs779269083 | |
pharmgkb | rs779269083 |
gwascentral | rs779269083 |
openSNP | rs779269083 |
23andMe | rs779269083 |
SNPshot | rs779269083 |
SNPdbe | rs779269083 |
MSV3d | rs779269083 |
GWAS Ctlg | rs779269083 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs779269083(A;A) rs779269083(T;T) |
Alt | rs779269083(A;A) rs779269083(T;T) |
Reference | Rs779269083(C;C) |
Significance | Other |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.94219175C>A |
CLNSRC | |
CLNACC | RCV000210166.1, |