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rs797046047

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797046047(G;T)
Make rs797046047(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position154170441
GeneTPM3
is asnp
is mentioned by
dbSNPrs797046047
ebirs797046047
HLIrs797046047
Exacrs797046047
Varsomers797046047
Maprs797046047
PheGenIrs797046047
hapmaprs797046047
1000 genomesrs797046047
hgdprs797046047
ensemblrs797046047
gopubmedrs797046047
geneviewrs797046047
scholarrs797046047
googlers797046047
pharmgkbrs797046047
gwascentralrs797046047
openSNPrs797046047
23andMers797046047
23andMe allrs797046047
SNP Nexus

SNPshotrs797046047
SNPdbers797046047
MSV3drs797046047
GWAS Ctlgrs797046047
Max Magnitude0
ClinVar
Risk rs797046047(T;T)
Alt rs797046047(T;T)
Reference rs797046047(G;G)
Significance Probable-Pathogenic
Disease Myopathy
Variation info
Gene TPM3
CLNDBN Myopathy
Reversed 1
HGVS NC_000001.10:g.154142917C>A
CLNSRC
CLNACC RCV000193345.1,