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rs397516242

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGC;CAGC) 0 common in clinvar
Make rs397516242(-;-)
Make rs397516242(-;CAGC)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431869
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516242
ebirs397516242
HLIrs397516242
Exacrs397516242
Varsomers397516242
Maprs397516242
PheGenIrs397516242
hapmaprs397516242
1000 genomesrs397516242
hgdprs397516242
ensemblrs397516242
gopubmedrs397516242
geneviewrs397516242
scholarrs397516242
googlers397516242
pharmgkbrs397516242
gwascentralrs397516242
openSNPrs397516242
23andMers397516242
23andMe allrs397516242
SNP Nexus

SNPshotrs397516242
SNPdbers397516242
MSV3drs397516242
GWAS Ctlgrs397516242
Max Magnitude0
ClinVar
Risk rs397516242(;)
Alt rs397516242(;)
Reference rs397516242(CAGC;CAGC)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23901078_23901081delGCTG
CLNSRC ClinVar
CLNACC RCV000035955.4, RCV000158835.1,