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rs199476311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199476311(A;A)
Make rs199476311(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position63059667
GeneTPM1
is asnp
is mentioned by
dbSNPrs199476311
ebirs199476311
HLIrs199476311
Exacrs199476311
Varsomers199476311
Maprs199476311
PheGenIrs199476311
hapmaprs199476311
1000 genomesrs199476311
hgdprs199476311
ensemblrs199476311
gopubmedrs199476311
geneviewrs199476311
scholarrs199476311
googlers199476311
pharmgkbrs199476311
gwascentralrs199476311
openSNPrs199476311
23andMers199476311
23andMe allrs199476311
SNP Nexus

SNPshotrs199476311
SNPdbers199476311
MSV3drs199476311
GWAS Ctlgrs199476311
Max Magnitude0
ClinVar
Risk rs199476311(A;A)
Alt rs199476311(A;A)
Reference rs199476311(G;G)
Significance Probable-Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene TPM1
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63351866G>A
CLNSRC Leiden Muscular Dystrophy pages (TPM1)
CLNACC RCV000024595.1, RCV000036336.2,


[PMID 20530761] The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.