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rs397516098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516098(A;A)
Make rs397516098(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23429044
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516098
ebirs397516098
HLIrs397516098
Exacrs397516098
Varsomers397516098
Maprs397516098
PheGenIrs397516098
hapmaprs397516098
1000 genomesrs397516098
hgdprs397516098
ensemblrs397516098
gopubmedrs397516098
geneviewrs397516098
scholarrs397516098
googlers397516098
pharmgkbrs397516098
gwascentralrs397516098
openSNPrs397516098
23andMers397516098
23andMe allrs397516098
SNP Nexus

SNPshotrs397516098
SNPdbers397516098
MSV3drs397516098
GWAS Ctlgrs397516098
Max Magnitude0
ClinVar
Risk rs397516098(A;A)
Alt rs397516098(A;A)
Reference rs397516098(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23898253C>T
CLNSRC ClinVar
CLNACC RCV000035713.2,