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rs397516089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516089(A;A)
Make rs397516089(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23429807
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516089
ebirs397516089
HLIrs397516089
Exacrs397516089
Varsomers397516089
Maprs397516089
PheGenIrs397516089
hapmaprs397516089
1000 genomesrs397516089
hgdprs397516089
ensemblrs397516089
gopubmedrs397516089
geneviewrs397516089
scholarrs397516089
googlers397516089
pharmgkbrs397516089
gwascentralrs397516089
openSNPrs397516089
23andMers397516089
23andMe allrs397516089
SNP Nexus

SNPshotrs397516089
SNPdbers397516089
MSV3drs397516089
GWAS Ctlgrs397516089
Max Magnitude0
ClinVar
Risk rs397516089(A,C;A,C)
Alt rs397516089(A,C;A,C)
Reference rs397516089(G;G)
Significance Pathogenic
Disease not specified Cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN not specified Cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23899016C>G; NC_000014.8:g.23899016C>T
CLNSRC ClinVar
CLNACC RCV000151297.2, RCV000157353.1, RCV000035698.3, RCV000158784.1, RCV000223685.1,