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rs730881151

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881151(G;T)
Make rs730881151(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position63042891
GeneTPM1
is asnp
is mentioned by
dbSNPrs730881151
ebirs730881151
HLIrs730881151
Exacrs730881151
Varsomers730881151
Maprs730881151
PheGenIrs730881151
hapmaprs730881151
1000 genomesrs730881151
hgdprs730881151
ensemblrs730881151
gopubmedrs730881151
geneviewrs730881151
scholarrs730881151
googlers730881151
pharmgkbrs730881151
gwascentralrs730881151
openSNPrs730881151
23andMers730881151
23andMe allrs730881151
SNP Nexus

SNPshotrs730881151
SNPdbers730881151
MSV3drs730881151
GWAS Ctlgrs730881151
Max Magnitude0
ClinVar
Risk rs730881151(T;T)
Alt rs730881151(T;T)
Reference rs730881151(G;G)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 3
Variation info
Gene TPM1
CLNDBN not specified Familial hypertrophic cardiomyopathy 3
Reversed 0
HGVS NC_000015.9:g.63335090G>T
CLNSRC
CLNACC RCV000168980.2, RCV000201492.1,