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rs397516276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516276(C;C)
Make rs397516276(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23430568
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516276
ebirs397516276
HLIrs397516276
Exacrs397516276
Varsomers397516276
Maprs397516276
PheGenIrs397516276
hapmaprs397516276
1000 genomesrs397516276
hgdprs397516276
ensemblrs397516276
gopubmedrs397516276
geneviewrs397516276
scholarrs397516276
googlers397516276
pharmgkbrs397516276
gwascentralrs397516276
openSNPrs397516276
23andMers397516276
23andMe allrs397516276
SNP Nexus

SNPshotrs397516276
SNPdbers397516276
MSV3drs397516276
GWAS Ctlgrs397516276
Max Magnitude0
ClinVar
Risk rs397516276(C;C)
Alt rs397516276(C;C)
Reference rs397516276(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23899777C>G
CLNSRC ClinVar
CLNACC RCV000036016.4,