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rs730881098

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881098(G;G)
Make rs730881098(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365613
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881098
ebirs730881098
HLIrs730881098
Exacrs730881098
Varsomers730881098
Maprs730881098
PheGenIrs730881098
hapmaprs730881098
1000 genomesrs730881098
hgdprs730881098
ensemblrs730881098
gopubmedrs730881098
geneviewrs730881098
scholarrs730881098
googlers730881098
pharmgkbrs730881098
gwascentralrs730881098
openSNPrs730881098
23andMers730881098
23andMe allrs730881098
SNP Nexus

SNPshotrs730881098
SNPdbers730881098
MSV3drs730881098
GWAS Ctlgrs730881098
Max Magnitude0
ClinVar
Risk rs730881098(G;G)
Alt rs730881098(G;G)
Reference rs730881098(T;T)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334741A>C
CLNSRC
CLNACC RCV000159279.1,