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rs730881131

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881131(C;C)
Make rs730881131(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position63057036
GeneTPM1
is asnp
is mentioned by
dbSNPrs730881131
ebirs730881131
HLIrs730881131
Exacrs730881131
Varsomers730881131
Maprs730881131
PheGenIrs730881131
hapmaprs730881131
1000 genomesrs730881131
hgdprs730881131
ensemblrs730881131
gopubmedrs730881131
geneviewrs730881131
scholarrs730881131
googlers730881131
pharmgkbrs730881131
gwascentralrs730881131
openSNPrs730881131
23andMers730881131
23andMe allrs730881131
SNP Nexus

SNPshotrs730881131
SNPdbers730881131
MSV3drs730881131
GWAS Ctlgrs730881131
Max Magnitude0
ClinVar
Risk rs730881131(C;C)
Alt rs730881131(C;C)
Reference rs730881131(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene TPM1
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63349235G>C
CLNSRC
CLNACC RCV000159357.1,