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rs397516110

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516110(C;C)
Make rs397516110(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23428546
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516110
ebirs397516110
HLIrs397516110
Exacrs397516110
Varsomers397516110
Maprs397516110
PheGenIrs397516110
hapmaprs397516110
1000 genomesrs397516110
hgdprs397516110
ensemblrs397516110
gopubmedrs397516110
geneviewrs397516110
scholarrs397516110
googlers397516110
pharmgkbrs397516110
gwascentralrs397516110
openSNPrs397516110
23andMers397516110
23andMe allrs397516110
SNP Nexus

SNPshotrs397516110
SNPdbers397516110
MSV3drs397516110
GWAS Ctlgrs397516110
Max Magnitude0
ClinVar
Risk rs397516110(C;C)
Alt rs397516110(C;C)
Reference rs397516110(T;T)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23897755A>G
CLNSRC ClinVar
CLNACC RCV000035729.4, RCV000201470.1,