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rs727504321

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs727504321(-;-)
Make rs727504321(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332827
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504321
ebirs727504321
HLIrs727504321
Exacrs727504321
Varsomers727504321
Maprs727504321
PheGenIrs727504321
hapmaprs727504321
1000 genomesrs727504321
hgdprs727504321
ensemblrs727504321
gopubmedrs727504321
geneviewrs727504321
scholarrs727504321
googlers727504321
pharmgkbrs727504321
gwascentralrs727504321
openSNPrs727504321
23andMers727504321
23andMe allrs727504321
SNP Nexus

SNPshotrs727504321
SNPdbers727504321
MSV3drs727504321
GWAS Ctlgrs727504321
Max Magnitude0
ClinVar
Risk rs727504321(;)
Alt rs727504321(;)
Reference rs727504321(TT;TT)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354378_47354379delAA
CLNSRC
CLNACC RCV000154411.3, RCV000211823.1,