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rs786204352

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204352(-;-)
Make rs786204352(-;T)
Make rs786204352(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47335100
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs786204352
ebirs786204352
HLIrs786204352
Exacrs786204352
Varsomers786204352
Maprs786204352
PheGenIrs786204352
hapmaprs786204352
1000 genomesrs786204352
hgdprs786204352
ensemblrs786204352
gopubmedrs786204352
geneviewrs786204352
scholarrs786204352
googlers786204352
pharmgkbrs786204352
gwascentralrs786204352
openSNPrs786204352
23andMers786204352
23andMe allrs786204352
SNP Nexus

SNPshotrs786204352
SNPdbers786204352
MSV3drs786204352
GWAS Ctlgrs786204352
Max Magnitude0
ClinVar
Risk rs786204352(T;T)
Alt rs786204352(T;T)
Reference rs786204352(;)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47356652dupA
CLNSRC
CLNACC RCV000168805.1,