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rs730881985

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs730881985(-;-)
Make rs730881985(-;TG)
Make rs730881985(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1219351
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881985
ebirs730881985
HLIrs730881985
Exacrs730881985
Varsomers730881985
Maprs730881985
PheGenIrs730881985
hapmaprs730881985
1000 genomesrs730881985
hgdprs730881985
ensemblrs730881985
gopubmedrs730881985
geneviewrs730881985
scholarrs730881985
googlers730881985
pharmgkbrs730881985
gwascentralrs730881985
openSNPrs730881985
23andMers730881985
23andMe allrs730881985
SNP Nexus

SNPshotrs730881985
SNPdbers730881985
MSV3drs730881985
GWAS Ctlgrs730881985
Max Magnitude0
ClinVar
Risk rs730881985(;)
Alt rs730881985(;)
Reference rs730881985(GT;GT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1219350_1219351delTG
CLNSRC
CLNACC RCV000161008.2,