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rs397516386

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516386(C;T)
Make rs397516386(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position63062585
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516386
ebirs397516386
HLIrs397516386
Exacrs397516386
Varsomers397516386
Maprs397516386
PheGenIrs397516386
hapmaprs397516386
1000 genomesrs397516386
hgdprs397516386
ensemblrs397516386
gopubmedrs397516386
geneviewrs397516386
scholarrs397516386
googlers397516386
pharmgkbrs397516386
gwascentralrs397516386
openSNPrs397516386
23andMers397516386
23andMe allrs397516386
SNP Nexus

SNPshotrs397516386
SNPdbers397516386
MSV3drs397516386
GWAS Ctlgrs397516386
Max Magnitude0
ClinVar
Risk rs397516386(T;T)
Alt rs397516386(T;T)
Reference rs397516386(C;C)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene TPM1
CLNDBN not specified Cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63354784C>T
CLNSRC
CLNACC RCV000036356.3, RCV000159384.1,