rs121913317
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121913317(G;T) |
Make rs121913317(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 1220503 |
Gene | STK11 |
is a | snp |
is | mentioned by |
dbSNP | rs121913317 |
dbSNP (classic) | rs121913317 |
ClinGen | rs121913317 |
ebi | rs121913317 |
HLI | rs121913317 |
Exac | rs121913317 |
Gnomad | rs121913317 |
Varsome | rs121913317 |
LitVar | rs121913317 |
Map | rs121913317 |
PheGenI | rs121913317 |
Biobank | rs121913317 |
1000 genomes | rs121913317 |
hgdp | rs121913317 |
ensembl | rs121913317 |
geneview | rs121913317 |
scholar | rs121913317 |
rs121913317 | |
pharmgkb | rs121913317 |
gwascentral | rs121913317 |
openSNP | rs121913317 |
23andMe | rs121913317 |
SNPshot | rs121913317 |
SNPdbe | rs121913317 |
MSV3d | rs121913317 |
GWAS Ctlg | rs121913317 |
Max Magnitude | 0 |
[PMID 27081308] Unraveling the Deleterious Effects of Cancer-Driven STK11 Mutants Through Conformational Sampling Approach
ClinVar | |
---|---|
Risk | rs121913317(A;A) rs121913317(T;T) |
Alt | rs121913317(A;A) rs121913317(T;T) |
Reference | Rs121913317(G;G) |
Significance | Probable-Pathogenic |
Disease | Neoplasm |
Variation | info |
Gene | STK11 |
CLNDBN | Neoplasm |
Reversed | 0 |
HGVS | NC_000019.9:g.1220502G>A; NC_000019.9:g.1220502G>T |
CLNSRC | |
CLNACC | RCV000426356.1, RCV000436703.1, |