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rs199476315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199476315(A;A)
Make rs199476315(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position63061723
GeneTPM1
is asnp
is mentioned by
dbSNPrs199476315
ebirs199476315
HLIrs199476315
Exacrs199476315
Varsomers199476315
Maprs199476315
PheGenIrs199476315
hapmaprs199476315
1000 genomesrs199476315
hgdprs199476315
ensemblrs199476315
gopubmedrs199476315
geneviewrs199476315
scholarrs199476315
googlers199476315
pharmgkbrs199476315
gwascentralrs199476315
openSNPrs199476315
23andMers199476315
23andMe allrs199476315
SNP Nexus

SNPshotrs199476315
SNPdbers199476315
MSV3drs199476315
GWAS Ctlgrs199476315
Max Magnitude0
ClinVar
Risk rs199476315(A;A)
Alt rs199476315(A;A)
Reference rs199476315(G;G)
Significance Other
Disease not provided Familial hypertrophic cardiomyopathy 3 Left ventricular noncompaction 9 Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene TPM1
CLNDBN not provided Familial hypertrophic cardiomyopathy 3 Left ventricular noncompaction 9 Primary familial hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000015.9:g.63353922G>A
CLNSRC Leiden Muscular Dystrophy pages (TPM1) OMIM Allelic Variant
CLNACC RCV000024578.2, RCV000036627.4, RCV000054795.24, RCV000208146.1, RCV000223758.1,


[PMID 12858563] Molecular epidemiology of hypertrophic cardiomyopathy.


[PMID 21551322] Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.