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rs202139499

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202139499(C;G)
Make rs202139499(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349804
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs202139499
ebirs202139499
HLIrs202139499
Exacrs202139499
Varsomers202139499
Maprs202139499
PheGenIrs202139499
hapmaprs202139499
1000 genomesrs202139499
hgdprs202139499
ensemblrs202139499
gopubmedrs202139499
geneviewrs202139499
scholarrs202139499
googlers202139499
pharmgkbrs202139499
gwascentralrs202139499
openSNPrs202139499
23andMers202139499
23andMe allrs202139499
SNP Nexus

SNPshotrs202139499
SNPdbers202139499
MSV3drs202139499
GWAS Ctlgrs202139499
Max Magnitude0
ClinVar
Risk rs202139499(G;G)
Alt rs202139499(G;G)
Reference rs202139499(C;C)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47371355C>G
CLNSRC
CLNACC RCV000035651.4, RCV000148684.1, RCV000172014.1, RCV000234354.1,