rs587776670
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;C) | 6.3 | Bannayan-Riley-Ruvalcaba syndrome |
(C;C) | 0 | common in clinvar |
Make rs587776670(-;-) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 87952211 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs587776670 |
dbSNP (classic) | rs587776670 |
ClinGen | rs587776670 |
ebi | rs587776670 |
HLI | rs587776670 |
Exac | rs587776670 |
Gnomad | rs587776670 |
Varsome | rs587776670 |
LitVar | rs587776670 |
Map | rs587776670 |
PheGenI | rs587776670 |
Biobank | rs587776670 |
1000 genomes | rs587776670 |
hgdp | rs587776670 |
ensembl | rs587776670 |
geneview | rs587776670 |
scholar | rs587776670 |
rs587776670 | |
pharmgkb | rs587776670 |
gwascentral | rs587776670 |
openSNP | rs587776670 |
23andMe | rs587776670 |
SNPshot | rs587776670 |
SNPdbe | rs587776670 |
MSV3d | rs587776670 |
GWAS Ctlg | rs587776670 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs587776670(-;-) |
Alt | rs587776670(-;-) |
Reference | Rs587776670(C;C) |
Significance | Pathogenic |
Disease | Bannayan-Riley-Ruvalcaba syndrome |
Variation | info |
Gene | PTEN |
CLNDBN | Bannayan-Riley-Ruvalcaba syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.89711968delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008269.3, |