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rs397516116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516116(C;C)
Make rs397516116(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23427861
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516116
ebirs397516116
HLIrs397516116
Exacrs397516116
Varsomers397516116
Maprs397516116
PheGenIrs397516116
hapmaprs397516116
1000 genomesrs397516116
hgdprs397516116
ensemblrs397516116
gopubmedrs397516116
geneviewrs397516116
scholarrs397516116
googlers397516116
pharmgkbrs397516116
gwascentralrs397516116
openSNPrs397516116
23andMers397516116
23andMe allrs397516116
SNP Nexus

SNPshotrs397516116
SNPdbers397516116
MSV3drs397516116
GWAS Ctlgrs397516116
Max Magnitude0
ClinVar
Risk rs397516116(C;C)
Alt rs397516116(C;C)
Reference rs397516116(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23897070A>G
CLNSRC ClinVar
CLNACC RCV000035736.3,