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rs587776699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776699(C;T)
Make rs587776699(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position47343281
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs587776699
ebirs587776699
HLIrs587776699
Exacrs587776699
Varsomers587776699
Maprs587776699
PheGenIrs587776699
hapmaprs587776699
1000 genomesrs587776699
hgdprs587776699
ensemblrs587776699
gopubmedrs587776699
geneviewrs587776699
scholarrs587776699
googlers587776699
pharmgkbrs587776699
gwascentralrs587776699
openSNPrs587776699
23andMers587776699
23andMe allrs587776699
SNP Nexus

SNPshotrs587776699
SNPdbers587776699
MSV3drs587776699
GWAS Ctlgrs587776699
Max Magnitude0
ClinVar
Risk rs587776699(T;T)
Alt rs587776699(T;T)
Reference rs587776699(C;C)
Significance Other
Disease Familial hypertrophic cardiomyopathy 4 not specified
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 not specified
Reversed 0
HGVS NC_000011.9:g.47364832C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009149.4, RCV000168768.2,