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rs397516154

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516154(A;A)
Make rs397516154(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424923
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516154
ebirs397516154
HLIrs397516154
Exacrs397516154
Varsomers397516154
Maprs397516154
PheGenIrs397516154
hapmaprs397516154
1000 genomesrs397516154
hgdprs397516154
ensemblrs397516154
gopubmedrs397516154
geneviewrs397516154
scholarrs397516154
googlers397516154
pharmgkbrs397516154
gwascentralrs397516154
openSNPrs397516154
23andMers397516154
23andMe allrs397516154
SNP Nexus

SNPshotrs397516154
SNPdbers397516154
MSV3drs397516154
GWAS Ctlgrs397516154
Max Magnitude0
ClinVar
Risk rs397516154(A;A)
Alt rs397516154(A;A)
Reference rs397516154(G;G)
Significance Probable-Pathogenic
Disease not specified Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Familial cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894132C>T
CLNSRC ClinVar
CLNACC RCV000035801.4, RCV000148956.1,