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rs730881969

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881969(A;A)
Make rs730881969(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1219345
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881969
ebirs730881969
HLIrs730881969
Exacrs730881969
Varsomers730881969
Maprs730881969
PheGenIrs730881969
hapmaprs730881969
1000 genomesrs730881969
hgdprs730881969
ensemblrs730881969
gopubmedrs730881969
geneviewrs730881969
scholarrs730881969
googlers730881969
pharmgkbrs730881969
gwascentralrs730881969
openSNPrs730881969
23andMers730881969
23andMe allrs730881969
SNP Nexus

SNPshotrs730881969
SNPdbers730881969
MSV3drs730881969
GWAS Ctlgrs730881969
Max Magnitude0
ClinVar
Risk rs730881969(A,T;A,T)
Alt rs730881969(A,T;A,T)
Reference rs730881969(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1219344C>A; NC_000019.9:g.1219344C>T
CLNSRC
CLNACC RCV000160988.1, RCV000163260.1, RCV000204600.1,