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rs587782958

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782958(A;A)
Make rs587782958(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333552
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs587782958
ebirs587782958
HLIrs587782958
Exacrs587782958
Varsomers587782958
Maprs587782958
PheGenIrs587782958
hapmaprs587782958
1000 genomesrs587782958
hgdprs587782958
ensemblrs587782958
gopubmedrs587782958
geneviewrs587782958
scholarrs587782958
googlers587782958
pharmgkbrs587782958
gwascentralrs587782958
openSNPrs587782958
23andMers587782958
23andMe allrs587782958
SNP Nexus

SNPshotrs587782958
SNPdbers587782958
MSV3drs587782958
GWAS Ctlgrs587782958
Max Magnitude0
ClinVar
Risk rs587782958(A;A)
Alt rs587782958(A;A)
Reference rs587782958(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355103C>T
CLNSRC
CLNACC RCV000143916.3, RCV000154317.4, RCV000158222.2, RCV000227910.1,