rs876660485
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6 | Breast cancer associated mutation |
Make rs876660485(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 108250861 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs876660485 |
dbSNP (classic) | rs876660485 |
ClinGen | rs876660485 |
ebi | rs876660485 |
HLI | rs876660485 |
Exac | rs876660485 |
Gnomad | rs876660485 |
Varsome | rs876660485 |
LitVar | rs876660485 |
Map | rs876660485 |
PheGenI | rs876660485 |
Biobank | rs876660485 |
1000 genomes | rs876660485 |
hgdp | rs876660485 |
ensembl | rs876660485 |
geneview | rs876660485 |
scholar | rs876660485 |
rs876660485 | |
pharmgkb | rs876660485 |
gwascentral | rs876660485 |
openSNP | rs876660485 |
23andMe | rs876660485 |
SNPshot | rs876660485 |
SNPdbe | rs876660485 |
MSV3d | rs876660485 |
GWAS Ctlg | rs876660485 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs876660485(T;T) |
Alt | rs876660485(T;T) |
Reference | Rs876660485(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | ATM |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108121588C>T |
CLNSRC | |
CLNACC | RCV000221369.1, RCV000486468.1, |