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rs397516264

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516264(A;A)
Make rs397516264(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431602
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516264
ebirs397516264
HLIrs397516264
Exacrs397516264
Varsomers397516264
Maprs397516264
PheGenIrs397516264
hapmaprs397516264
1000 genomesrs397516264
hgdprs397516264
ensemblrs397516264
gopubmedrs397516264
geneviewrs397516264
scholarrs397516264
googlers397516264
pharmgkbrs397516264
gwascentralrs397516264
openSNPrs397516264
23andMers397516264
23andMe allrs397516264
SNP Nexus

SNPshotrs397516264
SNPdbers397516264
MSV3drs397516264
GWAS Ctlgrs397516264
Max Magnitude0
ClinVar
Risk rs397516264(A;A)
Alt rs397516264(A;A)
Reference rs397516264(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1 not specified
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1 not specified
Reversed 1
HGVS NC_000014.8:g.23900811C>T
CLNSRC Centenary Institute
CLNACC RCV000035995.3, RCV000162339.1, RCV000168842.1,