rs773516672
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Breast cancer associated mutation |
(G;G) | 0 | common in clinvar |
Make rs773516672(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 108330355 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs773516672 |
dbSNP (classic) | rs773516672 |
ClinGen | rs773516672 |
ebi | rs773516672 |
HLI | rs773516672 |
Exac | rs773516672 |
Gnomad | rs773516672 |
Varsome | rs773516672 |
LitVar | rs773516672 |
Map | rs773516672 |
PheGenI | rs773516672 |
Biobank | rs773516672 |
1000 genomes | rs773516672 |
hgdp | rs773516672 |
ensembl | rs773516672 |
geneview | rs773516672 |
scholar | rs773516672 |
rs773516672 | |
pharmgkb | rs773516672 |
gwascentral | rs773516672 |
openSNP | rs773516672 |
23andMe | rs773516672 |
SNPshot | rs773516672 |
SNPdbe | rs773516672 |
MSV3d | rs773516672 |
GWAS Ctlg | rs773516672 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs773516672(A;A) |
Alt | rs773516672(A;A) |
Reference | Rs773516672(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | C11orf65 ATM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108201082G>A |
CLNSRC | |
CLNACC | RCV000236176.1, |