rs121909228
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 6.3 | Bannayan-Riley-Ruvalcaba syndrome |
Make rs121909228(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 87957984 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs121909228 |
dbSNP (classic) | rs121909228 |
ClinGen | rs121909228 |
ebi | rs121909228 |
HLI | rs121909228 |
Exac | rs121909228 |
Gnomad | rs121909228 |
Varsome | rs121909228 |
LitVar | rs121909228 |
Map | rs121909228 |
PheGenI | rs121909228 |
Biobank | rs121909228 |
1000 genomes | rs121909228 |
hgdp | rs121909228 |
ensembl | rs121909228 |
geneview | rs121909228 |
scholar | rs121909228 |
rs121909228 | |
pharmgkb | rs121909228 |
gwascentral | rs121909228 |
openSNP | rs121909228 |
23andMe | rs121909228 |
SNPshot | rs121909228 |
SNPdbe | rs121909228 |
MSV3d | rs121909228 |
GWAS Ctlg | rs121909228 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs121909228(T;T) |
Alt | rs121909228(T;T) |
Reference | Rs121909228(G;G) |
Significance | Pathogenic |
Disease | Bannayan-Riley-Ruvalcaba syndrome |
Variation | info |
Gene | PTEN |
CLNDBN | Bannayan-Riley-Ruvalcaba syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.89717741G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008274.2, |