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rs863224900

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224900(C;C)
Make rs863224900(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23428534
GeneMYH7
is asnp
is mentioned by
dbSNPrs863224900
ebirs863224900
HLIrs863224900
Exacrs863224900
Varsomers863224900
Maprs863224900
PheGenIrs863224900
hapmaprs863224900
1000 genomesrs863224900
hgdprs863224900
ensemblrs863224900
gopubmedrs863224900
geneviewrs863224900
scholarrs863224900
googlers863224900
pharmgkbrs863224900
gwascentralrs863224900
openSNPrs863224900
23andMers863224900
23andMe allrs863224900
SNP Nexus

SNPshotrs863224900
SNPdbers863224900
MSV3drs863224900
GWAS Ctlgrs863224900
Max Magnitude0
ClinVar
Risk rs863224900(C;C)
Alt rs863224900(C;C)
Reference rs863224900(T;T)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1S Familial hypertrophic cardiomyopathy 1 Myopathy Myosin storage myopathy Scapuloperoneal myopathy
Variation info
Gene MYH7
CLNDBN Dilated cardiomyopathy 1S Familial hypertrophic cardiomyopathy 1 Myopathy, distal, 1 Myosin storage myopathy Scapuloperoneal myopathy, MYH7-related
Reversed 1
HGVS NC_000014.8:g.23897743A>G
CLNSRC
CLNACC RCV000196427.1,