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rs36211715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs36211715(A;A)
Make rs36211715(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424839
GeneMYH7
is asnp
is mentioned by
dbSNPrs36211715
ebirs36211715
HLIrs36211715
Exacrs36211715
Varsomers36211715
Maprs36211715
PheGenIrs36211715
hapmaprs36211715
1000 genomesrs36211715
hgdprs36211715
ensemblrs36211715
gopubmedrs36211715
geneviewrs36211715
scholarrs36211715
googlers36211715
pharmgkbrs36211715
gwascentralrs36211715
openSNPrs36211715
23andMers36211715
23andMe allrs36211715
SNP Nexus

SNPshotrs36211715
SNPdbers36211715
MSV3drs36211715
GWAS Ctlgrs36211715
Max Magnitude0
OMIM160760
Desc
Variant0034
Relatedalso
ClinVar
Risk rs36211715(A;A)
Alt rs36211715(A;A)
Reference rs36211715(G;G)
Significance Other
Disease not specified Familial hypertrophic cardiomyopathy 1 Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1 Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894048C>A; NC_000014.8:g.23894048C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000223870.1, RCV000015177.28, RCV000157361.4, RCV000158555.2, RCV000233703.1,