Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881158

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881158(A;G)
Make rs730881158(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position63057037
GeneTPM1
is asnp
is mentioned by
dbSNPrs730881158
ebirs730881158
HLIrs730881158
Exacrs730881158
Varsomers730881158
Maprs730881158
PheGenIrs730881158
hapmaprs730881158
1000 genomesrs730881158
hgdprs730881158
ensemblrs730881158
gopubmedrs730881158
geneviewrs730881158
scholarrs730881158
googlers730881158
pharmgkbrs730881158
gwascentralrs730881158
openSNPrs730881158
23andMers730881158
23andMe allrs730881158
SNP Nexus

SNPshotrs730881158
SNPdbers730881158
MSV3drs730881158
GWAS Ctlgrs730881158
Max Magnitude0
ClinVar
Risk rs730881158(G;G)
Alt rs730881158(G;G)
Reference rs730881158(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene TPM1
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63349236A>G
CLNSRC
CLNACC RCV000159409.1,