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rs74315380

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315380(C;T)
Make rs74315380(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201364366
GeneTNNT2
is asnp
is mentioned by
dbSNPrs74315380
ebirs74315380
HLIrs74315380
Exacrs74315380
Varsomers74315380
Maprs74315380
PheGenIrs74315380
hapmaprs74315380
1000 genomesrs74315380
hgdprs74315380
ensemblrs74315380
gopubmedrs74315380
geneviewrs74315380
scholarrs74315380
googlers74315380
pharmgkbrs74315380
gwascentralrs74315380
openSNPrs74315380
23andMers74315380
23andMe allrs74315380
SNP Nexus

SNPshotrs74315380
SNPdbers74315380
MSV3drs74315380
GWAS Ctlgrs74315380
Max Magnitude0
OMIM191045
Desc
Variant0007
Relatedalso
OMIM191045
Desc
Variant0008
Relatedalso
ClinVar
Risk rs74315380(T;T)
Alt rs74315380(T;T)
Reference rs74315380(C;C)
Significance Other
Disease Left ventricular noncompaction 6 Primary dilated cardiomyopathy not provided
Variation info
Gene TNNT2
CLNDBN Left ventricular noncompaction 6 Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000001.10:g.201333494G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013226.27, RCV000030567.1, RCV000159291.1,