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rs397516266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516266(-;-)
Make rs397516266(-;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431584
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516266
ebirs397516266
HLIrs397516266
Exacrs397516266
Varsomers397516266
Maprs397516266
PheGenIrs397516266
hapmaprs397516266
1000 genomesrs397516266
hgdprs397516266
ensemblrs397516266
gopubmedrs397516266
geneviewrs397516266
scholarrs397516266
googlers397516266
pharmgkbrs397516266
gwascentralrs397516266
openSNPrs397516266
23andMers397516266
23andMe allrs397516266
SNP Nexus

SNPshotrs397516266
SNPdbers397516266
MSV3drs397516266
GWAS Ctlgrs397516266
Max Magnitude0
ClinVar
Risk rs397516266(;)
Alt rs397516266(;)
Reference rs397516266(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23900793delC
CLNSRC ClinVar
CLNACC RCV000035997.4,