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rs397515482

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515482(G;G)
Make rs397515482(G;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23430949
GeneMYH7
is asnp
is mentioned by
dbSNPrs397515482
ebirs397515482
HLIrs397515482
Exacrs397515482
Varsomers397515482
Maprs397515482
PheGenIrs397515482
hapmaprs397515482
1000 genomesrs397515482
hgdprs397515482
ensemblrs397515482
gopubmedrs397515482
geneviewrs397515482
scholarrs397515482
googlers397515482
pharmgkbrs397515482
gwascentralrs397515482
openSNPrs397515482
23andMers397515482
23andMe allrs397515482
SNP Nexus

SNPshotrs397515482
SNPdbers397515482
MSV3drs397515482
GWAS Ctlgrs397515482
Max Magnitude0
ClinVar
Risk rs397515482(G;G)
Alt rs397515482(G;G)
Reference rs397515482(T;T)
Significance Pathogenic
Disease Left ventricular noncompaction 5
Variation info
Gene MYH7
CLNDBN Left ventricular noncompaction 5
Reversed 1
HGVS NC_000014.8:g.23900158A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000056316.25,