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rs193922410

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922410(A;G)
Make rs193922410(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position63062248
GeneTPM1
is asnp
is mentioned by
dbSNPrs193922410
ebirs193922410
HLIrs193922410
Exacrs193922410
Varsomers193922410
Maprs193922410
PheGenIrs193922410
hapmaprs193922410
1000 genomesrs193922410
hgdprs193922410
ensemblrs193922410
gopubmedrs193922410
geneviewrs193922410
scholarrs193922410
googlers193922410
pharmgkbrs193922410
gwascentralrs193922410
openSNPrs193922410
23andMers193922410
23andMe allrs193922410
SNP Nexus

SNPshotrs193922410
SNPdbers193922410
MSV3drs193922410
GWAS Ctlgrs193922410
Max Magnitude0
ClinVar
Risk rs193922410(G;G)
Alt rs193922410(G;G)
Reference rs193922410(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene TPM1
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000015.9:g.63354447A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030569.1, RCV000159379.1,