rs398123320
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 6.3 | Hereditary cancer predisposing syndrome |
Make rs398123320(C;T) |
Make rs398123320(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 87933045 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs398123320 |
dbSNP (classic) | rs398123320 |
ClinGen | rs398123320 |
ebi | rs398123320 |
HLI | rs398123320 |
Exac | rs398123320 |
Gnomad | rs398123320 |
Varsome | rs398123320 |
LitVar | rs398123320 |
Map | rs398123320 |
PheGenI | rs398123320 |
Biobank | rs398123320 |
1000 genomes | rs398123320 |
hgdp | rs398123320 |
ensembl | rs398123320 |
geneview | rs398123320 |
scholar | rs398123320 |
rs398123320 | |
pharmgkb | rs398123320 |
gwascentral | rs398123320 |
openSNP | rs398123320 |
23andMe | rs398123320 |
SNPshot | rs398123320 |
SNPdbe | rs398123320 |
MSV3d | rs398123320 |
GWAS Ctlg | rs398123320 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs398123320(G;G) rs398123320(T;T) |
Alt | rs398123320(G;G) rs398123320(T;T) |
Reference | Rs398123320(C;C) |
Significance | Other |
Disease | not provided |
Variation | info |
Gene | PTEN |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.89692802C>G; NC_000010.10:g.89692802C>T |
CLNSRC | |
CLNACC | RCV000269234.1, RCV000078612.3, |