rs786204885
From SNPedia
Merged into | rs587781340 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GCAAAAGCCGCA;GCAAAAGCCGCA) | 0 | common in clinvar |
Make rs786204885(-;-) |
Make rs786204885(-;AAGCCGCAGCAA) |
Make rs786204885(AAGCCGCAGCAA;AAGCCGCAGCAA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 87863274 |
Gene | KLLN, PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs786204885 |
dbSNP (classic) | rs786204885 |
ClinGen | rs786204885 |
ebi | rs786204885 |
HLI | rs786204885 |
Exac | rs786204885 |
Gnomad | rs786204885 |
Varsome | rs786204885 |
LitVar | rs786204885 |
Map | rs786204885 |
PheGenI | rs786204885 |
Biobank | rs786204885 |
1000 genomes | rs786204885 |
hgdp | rs786204885 |
ensembl | rs786204885 |
geneview | rs786204885 |
scholar | rs786204885 |
rs786204885 | |
pharmgkb | rs786204885 |
gwascentral | rs786204885 |
openSNP | rs786204885 |
23andMe | rs786204885 |
SNPshot | rs786204885 |
SNPdbe | rs786204885 |
MSV3d | rs786204885 |
GWAS Ctlg | rs786204885 |
Status | Merged into rs587781340 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs786204885(GCAAAAGCCGCA;GCAAAAGCCGCA) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not specified |
Variation | info |
Gene | PTEN LOC101929706 KLLN |
CLNDBN | Hereditary cancer-predisposing syndrome not specified |
Reversed | 0 |
HGVS | NC_000010.10:g.89623031_89623042delAAGCCGCAGCAA |
CLNSRC | GeneDx |
CLNACC | RCV000129113.4, RCV000169826.2, |