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rs397516101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516101(A;A)
Make rs397516101(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23429004
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516101
ebirs397516101
HLIrs397516101
Exacrs397516101
Varsomers397516101
Maprs397516101
PheGenIrs397516101
hapmaprs397516101
1000 genomesrs397516101
hgdprs397516101
ensemblrs397516101
gopubmedrs397516101
geneviewrs397516101
scholarrs397516101
googlers397516101
pharmgkbrs397516101
gwascentralrs397516101
openSNPrs397516101
23andMers397516101
23andMe allrs397516101
SNP Nexus

SNPshotrs397516101
SNPdbers397516101
MSV3drs397516101
GWAS Ctlgrs397516101
Max Magnitude0
ClinVar
Risk rs397516101(A;A)
Alt rs397516101(A;A)
Reference rs397516101(G;G)
Significance Other
Disease not specified Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN not specified Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23898213C>A; NC_000014.8:g.23898213C>T
CLNSRC ClinVar
CLNACC RCV000223878.1, RCV000035718.2, RCV000158800.1, RCV000195545.1, RCV000201462.1,