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rs397516097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516097(A;A)
Make rs397516097(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23429089
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516097
ebirs397516097
HLIrs397516097
Exacrs397516097
Varsomers397516097
Maprs397516097
PheGenIrs397516097
hapmaprs397516097
1000 genomesrs397516097
hgdprs397516097
ensemblrs397516097
gopubmedrs397516097
geneviewrs397516097
scholarrs397516097
googlers397516097
pharmgkbrs397516097
gwascentralrs397516097
openSNPrs397516097
23andMers397516097
23andMe allrs397516097
SNP Nexus

SNPshotrs397516097
SNPdbers397516097
MSV3drs397516097
GWAS Ctlgrs397516097
Max Magnitude0
ClinVar
Risk rs397516097(A;A)
Alt rs397516097(A;A)
Reference rs397516097(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 1
HGVS NC_000014.8:g.23898298C>T
CLNSRC ClinVar
CLNACC RCV000035712.2, RCV000158792.2,