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rs397516166

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516166(C;C)
Make rs397516166(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424085
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516166
ebirs397516166
HLIrs397516166
Exacrs397516166
Varsomers397516166
Maprs397516166
PheGenIrs397516166
hapmaprs397516166
1000 genomesrs397516166
hgdprs397516166
ensemblrs397516166
gopubmedrs397516166
geneviewrs397516166
scholarrs397516166
googlers397516166
pharmgkbrs397516166
gwascentralrs397516166
openSNPrs397516166
23andMers397516166
23andMe allrs397516166
SNP Nexus

SNPshotrs397516166
SNPdbers397516166
MSV3drs397516166
GWAS Ctlgrs397516166
Max Magnitude0
ClinVar
Risk rs397516166(C;C)
Alt rs397516166(C;C)
Reference rs397516166(T;T)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23893294A>G
CLNSRC ClinVar
CLNACC RCV000035818.3,