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rs74315379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315379(C;T)
Make rs74315379(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201364336
GeneTNNT2
is asnp
is mentioned by
dbSNPrs74315379
ebirs74315379
HLIrs74315379
Exacrs74315379
Varsomers74315379
Maprs74315379
PheGenIrs74315379
hapmaprs74315379
1000 genomesrs74315379
hgdprs74315379
ensemblrs74315379
gopubmedrs74315379
geneviewrs74315379
scholarrs74315379
googlers74315379
pharmgkbrs74315379
gwascentralrs74315379
openSNPrs74315379
23andMers74315379
23andMe allrs74315379
SNP Nexus

SNPshotrs74315379
SNPdbers74315379
MSV3drs74315379
GWAS Ctlgrs74315379
Max Magnitude0
OMIM191045
Desc
Variant0007
Relatedalso
OMIM191045
Desc
Variant0008
Relatedalso
ClinVar
Risk rs74315379(A,T;A,T)
Alt rs74315379(A,T;A,T)
Reference rs74315379(C;C)
Significance Other
Disease Left ventricular noncompaction 6 Primary dilated cardiomyopathy not provided Familial hypertrophic cardiomyopathy 2 Cardiomyopathy not specified
Variation info
Gene TNNT2
CLNDBN Left ventricular noncompaction 6 Primary dilated cardiomyopathy not provided Familial hypertrophic cardiomyopathy 2 Cardiomyopathy not specified
Reversed 1
HGVS NC_000001.10:g.201333464G>A; NC_000001.10:g.201333464G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013225.24, RCV000157537.1, RCV000159296.1, RCV000168968.2, RCV000211866.1, RCV000036591.2,