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rs730881975

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881975(C;C)
Make rs730881975(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220699
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881975
ebirs730881975
HLIrs730881975
Exacrs730881975
Varsomers730881975
Maprs730881975
PheGenIrs730881975
hapmaprs730881975
1000 genomesrs730881975
hgdprs730881975
ensemblrs730881975
gopubmedrs730881975
geneviewrs730881975
scholarrs730881975
googlers730881975
pharmgkbrs730881975
gwascentralrs730881975
openSNPrs730881975
23andMers730881975
23andMe allrs730881975
SNP Nexus

SNPshotrs730881975
SNPdbers730881975
MSV3drs730881975
GWAS Ctlgrs730881975
Max Magnitude0
ClinVar
Risk rs730881975(C;C)
Alt rs730881975(C;C)
Reference rs730881975(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.1220698G>C
CLNSRC
CLNACC RCV000160994.1,