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rs863225271

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;T) 6.2 Familial Hypertrophic Cardiomyopathy
(T;T) 0 common in clinvar


Make rs863225271(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47342928
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs863225271
dbSNP (classic)rs863225271
ClinGenrs863225271
ebirs863225271
HLIrs863225271
Exacrs863225271
Gnomadrs863225271
Varsomers863225271
LitVarrs863225271
Maprs863225271
PheGenIrs863225271
Biobankrs863225271
1000 genomesrs863225271
hgdprs863225271
ensemblrs863225271
geneviewrs863225271
scholarrs863225271
googlers863225271
pharmgkbrs863225271
gwascentralrs863225271
openSNPrs863225271
23andMers863225271
SNPshotrs863225271
SNPdbers863225271
MSV3drs863225271
GWAS Ctlgrs863225271
Max Magnitude6.2
ClinVar
Risk rs863225271(-;-)
Alt rs863225271(-;-)
Reference Rs863225271(T;T)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000011.9:g.47364479delA
CLNSRC
CLNACC RCV000201912.1,