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rs397516390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516390(A;G)
Make rs397516390(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position63064081
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516390
ebirs397516390
HLIrs397516390
Exacrs397516390
Varsomers397516390
Maprs397516390
PheGenIrs397516390
hapmaprs397516390
1000 genomesrs397516390
hgdprs397516390
ensemblrs397516390
gopubmedrs397516390
geneviewrs397516390
scholarrs397516390
googlers397516390
pharmgkbrs397516390
gwascentralrs397516390
openSNPrs397516390
23andMers397516390
23andMe allrs397516390
SNP Nexus

SNPshotrs397516390
SNPdbers397516390
MSV3drs397516390
GWAS Ctlgrs397516390
Max Magnitude0
ClinVar
Risk rs397516390(G;G)
Alt rs397516390(G;G)
Reference rs397516390(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene TPM1
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63356280A>G
CLNSRC ClinVar
CLNACC RCV000036361.2,