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rs398123406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123406(G;T)
Make rs398123406(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position1222984
GeneSTK11
is asnp
is mentioned by
dbSNPrs398123406
ebirs398123406
HLIrs398123406
Exacrs398123406
Varsomers398123406
Maprs398123406
PheGenIrs398123406
hapmaprs398123406
1000 genomesrs398123406
hgdprs398123406
ensemblrs398123406
gopubmedrs398123406
geneviewrs398123406
scholarrs398123406
googlers398123406
pharmgkbrs398123406
gwascentralrs398123406
openSNPrs398123406
23andMers398123406
23andMe allrs398123406
SNP Nexus

SNPshotrs398123406
SNPdbers398123406
MSV3drs398123406
GWAS Ctlgrs398123406
Max Magnitude0
ClinVar
Risk rs398123406(T;T)
Alt rs398123406(T;T)
Reference rs398123406(G;G)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1222983G>T
CLNSRC ClinVar
CLNACC RCV000078915.4,