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rs121913317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913317(G;T)
Make rs121913317(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1220503
GeneSTK11
is asnp
is mentioned by
dbSNPrs121913317
dbSNP (old)rs121913317
ClinGenrs121913317
ebirs121913317
HLIrs121913317
Exacrs121913317
Gnomadrs121913317
Varsomers121913317
LitVarrs121913317
Maprs121913317
PheGenIrs121913317
Biobankrs121913317
1000 genomesrs121913317
hgdprs121913317
ensemblrs121913317
gopubmedrs121913317
geneviewrs121913317
scholarrs121913317
googlers121913317
pharmgkbrs121913317
gwascentralrs121913317
openSNPrs121913317
23andMers121913317
23andMe allrs121913317
SNPshotrs121913317
SNPdbers121913317
MSV3drs121913317
GWAS Ctlgrs121913317
Max Magnitude0

[PMID 27081308OA-icon.png] 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,