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rs730881971

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881971(G;T)
Make rs730881971(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1219414
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881971
ebirs730881971
HLIrs730881971
Exacrs730881971
Varsomers730881971
Maprs730881971
PheGenIrs730881971
hapmaprs730881971
1000 genomesrs730881971
hgdprs730881971
ensemblrs730881971
gopubmedrs730881971
geneviewrs730881971
scholarrs730881971
googlers730881971
pharmgkbrs730881971
gwascentralrs730881971
openSNPrs730881971
23andMers730881971
23andMe allrs730881971
SNP Nexus

SNPshotrs730881971
SNPdbers730881971
MSV3drs730881971
GWAS Ctlgrs730881971
Max Magnitude0
ClinVar
Risk rs730881971(T;T)
Alt rs730881971(T;T)
Reference rs730881971(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1219413G>T
CLNSRC
CLNACC RCV000160990.1,