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rs730881106

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881106(C;T)
Make rs730881106(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201362016
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881106
ebirs730881106
HLIrs730881106
Exacrs730881106
Varsomers730881106
Maprs730881106
PheGenIrs730881106
hapmaprs730881106
1000 genomesrs730881106
hgdprs730881106
ensemblrs730881106
gopubmedrs730881106
geneviewrs730881106
scholarrs730881106
googlers730881106
pharmgkbrs730881106
gwascentralrs730881106
openSNPrs730881106
23andMers730881106
23andMe allrs730881106
SNP Nexus

SNPshotrs730881106
SNPdbers730881106
MSV3drs730881106
GWAS Ctlgrs730881106
Max Magnitude0
ClinVar
Risk rs730881106(T;T)
Alt rs730881106(T;T)
Reference rs730881106(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201331144G>A
CLNSRC
CLNACC RCV000159307.1,