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rs786204338

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204338(G;T)
Make rs786204338(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47343021
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs786204338
ebirs786204338
HLIrs786204338
Exacrs786204338
Varsomers786204338
Maprs786204338
PheGenIrs786204338
hapmaprs786204338
1000 genomesrs786204338
hgdprs786204338
ensemblrs786204338
gopubmedrs786204338
geneviewrs786204338
scholarrs786204338
googlers786204338
pharmgkbrs786204338
gwascentralrs786204338
openSNPrs786204338
23andMers786204338
23andMe allrs786204338
SNP Nexus

SNPshotrs786204338
SNPdbers786204338
MSV3drs786204338
GWAS Ctlgrs786204338
Max Magnitude0
ClinVar
Risk rs786204338(T;T)
Alt rs786204338(T;T)
Reference rs786204338(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47364572C>A
CLNSRC
CLNACC RCV000168773.1,