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rs786204340

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204340(A;T)
Make rs786204340(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47342689
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs786204340
ebirs786204340
HLIrs786204340
Exacrs786204340
Varsomers786204340
Maprs786204340
PheGenIrs786204340
hapmaprs786204340
1000 genomesrs786204340
hgdprs786204340
ensemblrs786204340
gopubmedrs786204340
geneviewrs786204340
scholarrs786204340
googlers786204340
pharmgkbrs786204340
gwascentralrs786204340
openSNPrs786204340
23andMers786204340
23andMe allrs786204340
SNP Nexus

SNPshotrs786204340
SNPdbers786204340
MSV3drs786204340
GWAS Ctlgrs786204340
Max Magnitude0
ClinVar
Risk rs786204340(T;T)
Alt rs786204340(T;T)
Reference rs786204340(A;A)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47364240T>A
CLNSRC
CLNACC RCV000168779.1,