rs786204893
From SNPedia
Merged into | rs587782304 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAAT;AAAT) | 0 | common in clinvar |
Make rs786204893(-;-) |
Make rs786204893(-;TAAA) |
Make rs786204893(TAAA;TAAA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 87961079 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs786204893 |
dbSNP (classic) | rs786204893 |
ClinGen | rs786204893 |
ebi | rs786204893 |
HLI | rs786204893 |
Exac | rs786204893 |
Gnomad | rs786204893 |
Varsome | rs786204893 |
LitVar | rs786204893 |
Map | rs786204893 |
PheGenI | rs786204893 |
Biobank | rs786204893 |
1000 genomes | rs786204893 |
hgdp | rs786204893 |
ensembl | rs786204893 |
geneview | rs786204893 |
scholar | rs786204893 |
rs786204893 | |
pharmgkb | rs786204893 |
gwascentral | rs786204893 |
openSNP | rs786204893 |
23andMe | rs786204893 |
SNPshot | rs786204893 |
SNPdbe | rs786204893 |
MSV3d | rs786204893 |
GWAS Ctlg | rs786204893 |
Status | Merged into rs587782304 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs786204893(AAAT;AAAT) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | PTEN |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.89720836_89720839delTAAA |
CLNSRC | |
CLNACC | RCV000169834.3, RCV000212887.1, |