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rs397516237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516237(A;A)
Make rs397516237(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23432503
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516237
ebirs397516237
HLIrs397516237
Exacrs397516237
Varsomers397516237
Maprs397516237
PheGenIrs397516237
hapmaprs397516237
1000 genomesrs397516237
hgdprs397516237
ensemblrs397516237
gopubmedrs397516237
geneviewrs397516237
scholarrs397516237
googlers397516237
pharmgkbrs397516237
gwascentralrs397516237
openSNPrs397516237
23andMers397516237
23andMe allrs397516237
SNP Nexus

SNPshotrs397516237
SNPdbers397516237
MSV3drs397516237
GWAS Ctlgrs397516237
Max Magnitude0
ClinVar
Risk rs397516237(A;A)
Alt rs397516237(A;A)
Reference rs397516237(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901712C>T
CLNSRC ClinVar
CLNACC RCV000035948.4,