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rs786204332

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204332(-;-)
Make rs786204332(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47347899
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs786204332
ebirs786204332
HLIrs786204332
Exacrs786204332
Varsomers786204332
Maprs786204332
PheGenIrs786204332
hapmaprs786204332
1000 genomesrs786204332
hgdprs786204332
ensemblrs786204332
gopubmedrs786204332
geneviewrs786204332
scholarrs786204332
googlers786204332
pharmgkbrs786204332
gwascentralrs786204332
openSNPrs786204332
23andMers786204332
23andMe allrs786204332
SNP Nexus

SNPshotrs786204332
SNPdbers786204332
MSV3drs786204332
GWAS Ctlgrs786204332
Max Magnitude0
ClinVar
Risk rs786204332(;)
Alt rs786204332(;)
Reference rs786204332(T;T)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47369450delA
CLNSRC
CLNACC RCV000168756.1,