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rs397516372

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516372(C;G)
Make rs397516372(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position63059645
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516372
ebirs397516372
HLIrs397516372
Exacrs397516372
Varsomers397516372
Maprs397516372
PheGenIrs397516372
hapmaprs397516372
1000 genomesrs397516372
hgdprs397516372
ensemblrs397516372
gopubmedrs397516372
geneviewrs397516372
scholarrs397516372
googlers397516372
pharmgkbrs397516372
gwascentralrs397516372
openSNPrs397516372
23andMers397516372
23andMe allrs397516372
SNP Nexus

SNPshotrs397516372
SNPdbers397516372
MSV3drs397516372
GWAS Ctlgrs397516372
Max Magnitude0
ClinVar
Risk rs397516372(G;G)
Alt rs397516372(G;G)
Reference rs397516372(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene TPM1
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63351844C>G
CLNSRC ClinVar
CLNACC RCV000036333.2,