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rs397516267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516267(A;A)
Make rs397516267(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431480
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516267
ebirs397516267
HLIrs397516267
Exacrs397516267
Varsomers397516267
Maprs397516267
PheGenIrs397516267
hapmaprs397516267
1000 genomesrs397516267
hgdprs397516267
ensemblrs397516267
gopubmedrs397516267
geneviewrs397516267
scholarrs397516267
googlers397516267
pharmgkbrs397516267
gwascentralrs397516267
openSNPrs397516267
23andMers397516267
23andMe allrs397516267
SNP Nexus

SNPshotrs397516267
SNPdbers397516267
MSV3drs397516267
GWAS Ctlgrs397516267
Max Magnitude0
ClinVar
Risk rs397516267(A;A)
Alt rs397516267(A;A)
Reference rs397516267(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23900689C>T
CLNSRC ClinVar
CLNACC RCV000035999.3,