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rs863225269

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225269(-;C)
Make rs863225269(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23392970
GeneMYH6
is asnp
is mentioned by
dbSNPrs863225269
dbSNP (old)rs863225269
ClinGenrs863225269
ebirs863225269
HLIrs863225269
Exacrs863225269
Gnomadrs863225269
Varsomers863225269
Maprs863225269
PheGenIrs863225269
Biobankrs863225269
1000 genomesrs863225269
hgdprs863225269
ensemblrs863225269
gopubmedrs863225269
geneviewrs863225269
scholarrs863225269
googlers863225269
pharmgkbrs863225269
gwascentralrs863225269
openSNPrs863225269
23andMers863225269
23andMe allrs863225269
SNP Nexus

SNPshotrs863225269
SNPdbers863225269
MSV3drs863225269
GWAS Ctlgrs863225269
Max Magnitude0
ClinVar
Risk rs863225269(C;C)
Alt rs863225269(C;C)
Reference Rs863225269(-;-)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH6
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23862180dupG
CLNSRC
CLNACC RCV000201905.1,