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rs786205864

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205864(-;-)
Make rs786205864(-;C)
Make rs786205864(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1221322
GeneSTK11
is asnp
is mentioned by
dbSNPrs786205864
ebirs786205864
HLIrs786205864
Exacrs786205864
Varsomers786205864
Maprs786205864
PheGenIrs786205864
hapmaprs786205864
1000 genomesrs786205864
hgdprs786205864
ensemblrs786205864
gopubmedrs786205864
geneviewrs786205864
scholarrs786205864
googlers786205864
pharmgkbrs786205864
gwascentralrs786205864
openSNPrs786205864
23andMers786205864
23andMe allrs786205864
SNP Nexus

SNPshotrs786205864
SNPdbers786205864
MSV3drs786205864
GWAS Ctlgrs786205864
Max Magnitude0
ClinVar
Risk rs786205864(C;C)
Alt rs786205864(C;C)
Reference rs786205864(;)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1221321dupC
CLNSRC
CLNACC RCV000172824.1,