rs555895
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs555895(G;G) |
Make rs555895(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 87961150 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs555895 |
dbSNP (classic) | rs555895 |
ClinGen | rs555895 |
ebi | rs555895 |
HLI | rs555895 |
Exac | rs555895 |
Gnomad | rs555895 |
Varsome | rs555895 |
LitVar | rs555895 |
Map | rs555895 |
PheGenI | rs555895 |
Biobank | rs555895 |
1000 genomes | rs555895 |
hgdp | rs555895 |
ensembl | rs555895 |
geneview | rs555895 |
scholar | rs555895 |
rs555895 | |
pharmgkb | rs555895 |
gwascentral | rs555895 |
openSNP | rs555895 |
23andMe | rs555895 |
SNPshot | rs555895 |
SNPdbe | rs555895 |
MSV3d | rs555895 |
GWAS Ctlg | rs555895 |
GMAF | 0.4339 |
Max Magnitude | 0 |
[PMID 23068025] Association of PTEN genetic polymorphisms with atherosclerotic cerebral infarction in the Han Chinese population [PMID 17033968] Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
ClinVar | |
---|---|
Risk | rs555895(G;G) |
Alt | rs555895(G;G) |
Reference | Rs555895(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | PTEN |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000010.10:g.89720907T>G |
CLNSRC | ClinVar |
CLNACC | RCV000078603.4, |
[PMID 26541596] Association of genetic polymorphisms in PTEN and additional gene-gene interaction with risk of esophageal squamous cell carcinoma in Chinese Han population