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rs397516258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516258(C;C)
Make rs397516258(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431798
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516258
ebirs397516258
HLIrs397516258
Exacrs397516258
Varsomers397516258
Maprs397516258
PheGenIrs397516258
hapmaprs397516258
1000 genomesrs397516258
hgdprs397516258
ensemblrs397516258
gopubmedrs397516258
geneviewrs397516258
scholarrs397516258
googlers397516258
pharmgkbrs397516258
gwascentralrs397516258
openSNPrs397516258
23andMers397516258
23andMe allrs397516258
SNP Nexus

SNPshotrs397516258
SNPdbers397516258
MSV3drs397516258
GWAS Ctlgrs397516258
Max Magnitude0
ClinVar
Risk rs397516258(C;C)
Alt rs397516258(C;C)
Reference rs397516258(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 1
HGVS NC_000014.8:g.23901007A>G
CLNSRC ClinVar
CLNACC RCV000035988.3, RCV000158747.2,