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rs1057520042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520042(C;C)
Make rs1057520042(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1222988
GeneSTK11
is asnp
is mentioned by
dbSNPrs1057520042
dbSNP (old)rs1057520042
ClinGenrs1057520042
ebirs1057520042
HLIrs1057520042
Exacrs1057520042
Gnomadrs1057520042
Varsomers1057520042
Maprs1057520042
PheGenIrs1057520042
Biobankrs1057520042
1000 genomesrs1057520042
hgdprs1057520042
ensemblrs1057520042
gopubmedrs1057520042
geneviewrs1057520042
scholarrs1057520042
googlers1057520042
pharmgkbrs1057520042
gwascentralrs1057520042
openSNPrs1057520042
23andMers1057520042
23andMe allrs1057520042
SNPshotrs1057520042
SNPdbers1057520042
MSV3drs1057520042
GWAS Ctlgrs1057520042
Max Magnitude0
ClinVar
Risk rs1057520042(C;C)
Alt rs1057520042(C;C)
Reference Rs1057520042(G;G)
Significance Probable-Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1222987G>C
CLNSRC
CLNACC RCV000435765.1,