rs876661177
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs876661177(G;G) |
Make rs876661177(G;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 87931078 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs876661177 |
dbSNP (classic) | rs876661177 |
ClinGen | rs876661177 |
ebi | rs876661177 |
HLI | rs876661177 |
Exac | rs876661177 |
Gnomad | rs876661177 |
Varsome | rs876661177 |
LitVar | rs876661177 |
Map | rs876661177 |
PheGenI | rs876661177 |
Biobank | rs876661177 |
1000 genomes | rs876661177 |
hgdp | rs876661177 |
ensembl | rs876661177 |
geneview | rs876661177 |
scholar | rs876661177 |
rs876661177 | |
pharmgkb | rs876661177 |
gwascentral | rs876661177 |
openSNP | rs876661177 |
23andMe | rs876661177 |
SNPshot | rs876661177 |
SNPdbe | rs876661177 |
MSV3d | rs876661177 |
GWAS Ctlg | rs876661177 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661177(G;G) |
Alt | rs876661177(G;G) |
Reference | Rs876661177(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PTEN |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.89690835T>G |
CLNSRC | |
CLNACC | RCV000221920.1, |