rs767623493
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;T) | 6.3 | Hereditary cancer predisposing syndrome |
(T;T) | 0 | common in clinvar |
Make rs767623493(C;C) |
Make rs767623493(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 87957968 |
Gene | PTEN |
is a | snp |
is | mentioned by |
dbSNP | rs767623493 |
dbSNP (classic) | rs767623493 |
ClinGen | rs767623493 |
ebi | rs767623493 |
HLI | rs767623493 |
Exac | rs767623493 |
Gnomad | rs767623493 |
Varsome | rs767623493 |
LitVar | rs767623493 |
Map | rs767623493 |
PheGenI | rs767623493 |
Biobank | rs767623493 |
1000 genomes | rs767623493 |
hgdp | rs767623493 |
ensembl | rs767623493 |
geneview | rs767623493 |
scholar | rs767623493 |
rs767623493 | |
pharmgkb | rs767623493 |
gwascentral | rs767623493 |
openSNP | rs767623493 |
23andMe | rs767623493 |
SNPshot | rs767623493 |
SNPdbe | rs767623493 |
MSV3d | rs767623493 |
GWAS Ctlg | rs767623493 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs767623493(A;A) rs767623493(C;C) |
Alt | rs767623493(A;A) rs767623493(C;C) |
Reference | Rs767623493(T;T) |
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.89717725T>A; NC_000010.10:g.89717725T>C |
CLNSRC | |
CLNACC | RCV000218967.1, RCV000480028.1, RCV000164253.1, |