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

rs397516224

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516224(-;-)
Make rs397516224(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23432684
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516224
ebirs397516224
HLIrs397516224
Exacrs397516224
Varsomers397516224
Maprs397516224
PheGenIrs397516224
hapmaprs397516224
1000 genomesrs397516224
hgdprs397516224
ensemblrs397516224
gopubmedrs397516224
geneviewrs397516224
scholarrs397516224
googlers397516224
pharmgkbrs397516224
gwascentralrs397516224
openSNPrs397516224
23andMers397516224
23andMe allrs397516224
SNP Nexus

SNPshotrs397516224
SNPdbers397516224
MSV3drs397516224
GWAS Ctlgrs397516224
Max Magnitude0
ClinVar
Risk rs397516224(;)
Alt rs397516224(;)
Reference rs397516224(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23901893delG
CLNSRC
CLNACC RCV000035922.3,