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rs730881958

From SNPedia

Orientationplus
Geno Mag Summary
(TCATCGGCAAGT;TCATCGGCAAGT) 0 common in clinvar
Make rs730881958(-;-)
Make rs730881958(-;TCATCGGCAAGT)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1207047
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881958
ebirs730881958
HLIrs730881958
Exacrs730881958
Varsomers730881958
Maprs730881958
PheGenIrs730881958
hapmaprs730881958
1000 genomesrs730881958
hgdprs730881958
ensemblrs730881958
gopubmedrs730881958
geneviewrs730881958
scholarrs730881958
googlers730881958
pharmgkbrs730881958
gwascentralrs730881958
openSNPrs730881958
23andMers730881958
23andMe allrs730881958
SNP Nexus

SNPshotrs730881958
SNPdbers730881958
MSV3drs730881958
GWAS Ctlgrs730881958
Max Magnitude0
ClinVar
Risk rs730881958(;)
Alt rs730881958(;)
Reference rs730881958(TCATCGGCAAGT;TCATCGGCAAGT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1207046_1207057delTCATCGGCAAGT
CLNSRC
CLNACC RCV000160967.1,