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rs201278114

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201278114(C;G)
Make rs201278114(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47352635
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs201278114
ebirs201278114
HLIrs201278114
Exacrs201278114
Varsomers201278114
Maprs201278114
PheGenIrs201278114
hapmaprs201278114
1000 genomesrs201278114
hgdprs201278114
ensemblrs201278114
gopubmedrs201278114
geneviewrs201278114
scholarrs201278114
googlers201278114
pharmgkbrs201278114
gwascentralrs201278114
openSNPrs201278114
23andMers201278114
23andMe allrs201278114
SNP Nexus

SNPshotrs201278114
SNPdbers201278114
MSV3drs201278114
GWAS Ctlgrs201278114
Max Magnitude0
ClinVar
Risk rs201278114(G;G)
Alt rs201278114(G;G)
Reference rs201278114(C;C)
Significance Other
Disease Familial hypertrophic cardiomyopathy 1 Primary familial hypertrophic cardiomyopathy not specified Left ventricular hypertrophy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 1 Primary familial hypertrophic cardiomyopathy not specified Left ventricular hypertrophy
Reversed 0
HGVS NC_000011.9:g.47374186C>A; NC_000011.9:g.47374186C>G
CLNSRC
CLNACC RCV000201920.1, RCV000148668.2, RCV000151176.4, RCV000234987.1,