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rs121964855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964855(A;A)
Make rs121964855(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201365638
GeneTNNT2
is asnp
is mentioned by
dbSNPrs121964855
ebirs121964855
HLIrs121964855
Exacrs121964855
Varsomers121964855
Maprs121964855
PheGenIrs121964855
hapmaprs121964855
1000 genomesrs121964855
hgdprs121964855
ensemblrs121964855
gopubmedrs121964855
geneviewrs121964855
scholarrs121964855
googlers121964855
pharmgkbrs121964855
gwascentralrs121964855
openSNPrs121964855
23andMers121964855
23andMe allrs121964855
SNP Nexus

SNPshotrs121964855
SNPdbers121964855
MSV3drs121964855
GWAS Ctlgrs121964855
Max Magnitude0
OMIM191045
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964855(A;A)
Alt rs121964855(A;A)
Reference rs121964855(T;T)
Significance Other
Disease Familial hypertrophic cardiomyopathy 2 Left ventricular noncompaction 6 Familial restrictive cardiomyopathy 3 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Familial hypertrophic cardiomyopathy 2 Left ventricular noncompaction 6 Familial restrictive cardiomyopathy 3 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334766A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013217.28, RCV000013218.16, RCV000013219.23, RCV000159272.2, RCV000211864.1,