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rs1057524439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(T;T) 0 common in clinvar


Make rs1057524439(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1221955
GeneSTK11
is asnp
is mentioned by
dbSNPrs1057524439
dbSNP (old)rs1057524439
ClinGenrs1057524439
ebirs1057524439
HLIrs1057524439
Exacrs1057524439
Gnomadrs1057524439
Varsomers1057524439
LitVarrs1057524439
Maprs1057524439
PheGenIrs1057524439
Biobankrs1057524439
1000 genomesrs1057524439
hgdprs1057524439
ensemblrs1057524439
gopubmedrs1057524439
geneviewrs1057524439
scholarrs1057524439
googlers1057524439
pharmgkbrs1057524439
gwascentralrs1057524439
openSNPrs1057524439
23andMers1057524439
23andMe allrs1057524439
SNPshotrs1057524439
SNPdbers1057524439
MSV3drs1057524439
GWAS Ctlgrs1057524439
Max Magnitude5.8
ClinVar
Risk rs1057524439(C;C)
Alt rs1057524439(C;C)
Reference Rs1057524439(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STK11
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1221954T>C
CLNSRC
CLNACC RCV000434265.1,