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rs398123279

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs398123279(-;-)
Make rs398123279(-;GT)
ReferenceGRCh38 38.1/141
Chromosome11
Position47342139
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs398123279
ebirs398123279
HLIrs398123279
Exacrs398123279
Varsomers398123279
Maprs398123279
PheGenIrs398123279
hapmaprs398123279
1000 genomesrs398123279
hgdprs398123279
ensemblrs398123279
gopubmedrs398123279
geneviewrs398123279
scholarrs398123279
googlers398123279
pharmgkbrs398123279
gwascentralrs398123279
openSNPrs398123279
23andMers398123279
23andMe allrs398123279
SNP Nexus

SNPshotrs398123279
SNPdbers398123279
MSV3drs398123279
GWAS Ctlgrs398123279
Max Magnitude0
ClinVar
Risk rs398123279(;)
Alt rs398123279(;)
Reference rs398123279(GT;GT)
Significance Other
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47363690_47363691delAC
CLNSRC HGMD
CLNACC RCV000078449.5, RCV000208043.2,