rs1085308048
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Chromosome | 10 |
Position | 87933175 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs1085308048 |
dbSNP (classic) | rs1085308048 |
ClinGen | rs1085308048 |
ebi | rs1085308048 |
HLI | rs1085308048 |
Exac | rs1085308048 |
Gnomad | rs1085308048 |
Varsome | rs1085308048 |
LitVar | rs1085308048 |
Map | rs1085308048 |
PheGenI | rs1085308048 |
Biobank | rs1085308048 |
1000 genomes | rs1085308048 |
hgdp | rs1085308048 |
ensembl | rs1085308048 |
geneview | rs1085308048 |
scholar | rs1085308048 |
rs1085308048 | |
pharmgkb | rs1085308048 |
gwascentral | rs1085308048 |
openSNP | rs1085308048 |
23andMe | rs1085308048 |
SNPshot | rs1085308048 |
SNPdbe | rs1085308048 |
MSV3d | rs1085308048 |
GWAS Ctlg | rs1085308048 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1085308048(G;G) |
Alt | rs1085308048(G;G) |
Reference | Rs1085308048(T;T) |
Significance | Pathogenic |
Disease | PTEN hamartoma tumor syndrome |
Variation | info |
Gene | PTEN |
CLNDBN | PTEN hamartoma tumor syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.89692932T>G |
CLNSRC | |
CLNACC | RCV000490603.1, |