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rs727504334

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504334(A;A)
Make rs727504334(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47338680
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504334
ebirs727504334
HLIrs727504334
Exacrs727504334
Varsomers727504334
Maprs727504334
PheGenIrs727504334
hapmaprs727504334
1000 genomesrs727504334
hgdprs727504334
ensemblrs727504334
gopubmedrs727504334
geneviewrs727504334
scholarrs727504334
googlers727504334
pharmgkbrs727504334
gwascentralrs727504334
openSNPrs727504334
23andMers727504334
23andMe allrs727504334
SNP Nexus

SNPshotrs727504334
SNPdbers727504334
MSV3drs727504334
GWAS Ctlgrs727504334
Max Magnitude0
ClinVar
Risk rs727504334(A;A)
Alt rs727504334(A;A)
Reference rs727504334(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47360231C>T
CLNSRC
CLNACC RCV000154446.2,