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rs397516152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516152(C;G)
Make rs397516152(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424946
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516152
ebirs397516152
HLIrs397516152
Exacrs397516152
Varsomers397516152
Maprs397516152
PheGenIrs397516152
hapmaprs397516152
1000 genomesrs397516152
hgdprs397516152
ensemblrs397516152
gopubmedrs397516152
geneviewrs397516152
scholarrs397516152
googlers397516152
pharmgkbrs397516152
gwascentralrs397516152
openSNPrs397516152
23andMers397516152
23andMe allrs397516152
SNP Nexus

SNPshotrs397516152
SNPdbers397516152
MSV3drs397516152
GWAS Ctlgrs397516152
Max Magnitude0
ClinVar
Risk rs397516152(G;G)
Alt rs397516152(G;G)
Reference rs397516152(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894155G>C
CLNSRC ClinVar
CLNACC RCV000035798.3,