rs397518442
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397518442(-;-) |
Make rs397518442(-;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 1220633 |
Gene | STK11 |
is a | snp |
is | mentioned by |
dbSNP | rs397518442 |
dbSNP (classic) | rs397518442 |
ClinGen | rs397518442 |
ebi | rs397518442 |
HLI | rs397518442 |
Exac | rs397518442 |
Gnomad | rs397518442 |
Varsome | rs397518442 |
LitVar | rs397518442 |
Map | rs397518442 |
PheGenI | rs397518442 |
Biobank | rs397518442 |
1000 genomes | rs397518442 |
hgdp | rs397518442 |
ensembl | rs397518442 |
geneview | rs397518442 |
scholar | rs397518442 |
rs397518442 | |
pharmgkb | rs397518442 |
gwascentral | rs397518442 |
openSNP | rs397518442 |
23andMe | rs397518442 |
SNPshot | rs397518442 |
SNPdbe | rs397518442 |
MSV3d | rs397518442 |
GWAS Ctlg | rs397518442 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397518442(-;-) |
Alt | rs397518442(-;-) |
Reference | Rs397518442(C;C) |
Significance | Pathogenic |
Disease | Carcinoma of pancreas |
Variation | info |
Gene | STK11 |
CLNDBN | Carcinoma of pancreas |
Reversed | 0 |
HGVS | NC_000019.9:g.1220632delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000007879.9, |