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

rs397516246

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516246(A;A)
Make rs397516246(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23415212
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516246
ebirs397516246
HLIrs397516246
Exacrs397516246
Varsomers397516246
Maprs397516246
PheGenIrs397516246
hapmaprs397516246
1000 genomesrs397516246
hgdprs397516246
ensemblrs397516246
gopubmedrs397516246
geneviewrs397516246
scholarrs397516246
googlers397516246
pharmgkbrs397516246
gwascentralrs397516246
openSNPrs397516246
23andMers397516246
23andMe allrs397516246
SNP Nexus

SNPshotrs397516246
SNPdbers397516246
MSV3drs397516246
GWAS Ctlgrs397516246
Max Magnitude0
ClinVar
Risk rs397516246(A;A)
Alt rs397516246(A;A)
Reference rs397516246(G;G)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23884421C>T
CLNSRC ClinVar
CLNACC RCV000035959.3, RCV000234735.1,