rs398123406
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;G) | 5.8 | STK11 gene mutation associated with Peutz-Jeghers syndrome |
(G;G) | 0 | common in clinvar |
(G;T) | 5.8 | STK11 gene mutation associated with Peutz-Jeghers syndrome |
Make rs398123406(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 1222984 |
Gene | STK11 |
is a | snp |
is | mentioned by |
dbSNP | rs398123406 |
dbSNP (classic) | rs398123406 |
ClinGen | rs398123406 |
ebi | rs398123406 |
HLI | rs398123406 |
Exac | rs398123406 |
Gnomad | rs398123406 |
Varsome | rs398123406 |
LitVar | rs398123406 |
Map | rs398123406 |
PheGenI | rs398123406 |
Biobank | rs398123406 |
1000 genomes | rs398123406 |
hgdp | rs398123406 |
ensembl | rs398123406 |
geneview | rs398123406 |
scholar | rs398123406 |
rs398123406 | |
pharmgkb | rs398123406 |
gwascentral | rs398123406 |
openSNP | rs398123406 |
23andMe | rs398123406 |
SNPshot | rs398123406 |
SNPdbe | rs398123406 |
MSV3d | rs398123406 |
GWAS Ctlg | rs398123406 |
Max Magnitude | 5.8 |
rs398123406, also known as c.921-1G>T, represents a rare variant in the STK11 gene on chromosome 19.
In ClinVar, there is one group reporting the rs398123406(T) variant to be a pathogenic mutation associated with Peutz-Jeghers syndrome, presumably inherited in a dominant manner.
ClinVar | |
---|---|
Risk | rs398123406(C;C) rs398123406(T;T) |
Alt | rs398123406(C;C) rs398123406(T;T) |
Reference | Rs398123406(G;G) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome Peutz-Jeghers syndrome |
Variation | info |
Gene | STK11 |
CLNDBN | not provided Hereditary cancer-predisposing syndrome Peutz-Jeghers syndrome |
Reversed | 0 |
HGVS | NC_000019.9:g.1222983G>C; NC_000019.9:g.1222983G>T |
CLNSRC | ClinVar |
CLNACC | RCV000414694.1, RCV000492537.1, RCV000078915.4, |