Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516159

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs397516159(-;-)
Make rs397516159(-;GAG)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424823
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516159
ebirs397516159
HLIrs397516159
Exacrs397516159
Varsomers397516159
Maprs397516159
PheGenIrs397516159
hapmaprs397516159
1000 genomesrs397516159
hgdprs397516159
ensemblrs397516159
gopubmedrs397516159
geneviewrs397516159
scholarrs397516159
googlers397516159
pharmgkbrs397516159
gwascentralrs397516159
openSNPrs397516159
23andMers397516159
23andMe allrs397516159
SNP Nexus

SNPshotrs397516159
SNPdbers397516159
MSV3drs397516159
GWAS Ctlgrs397516159
Max Magnitude0
ClinVar
Risk rs397516159(;)
Alt rs397516159(;)
Reference rs397516159(GAG;GAG)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23894032_23894034delCTC
CLNSRC ClinVar
CLNACC RCV000035809.4,