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rs727504305

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504305(A;A)
Make rs727504305(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332974
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504305
ebirs727504305
HLIrs727504305
Exacrs727504305
Varsomers727504305
Maprs727504305
PheGenIrs727504305
hapmaprs727504305
1000 genomesrs727504305
hgdprs727504305
ensemblrs727504305
gopubmedrs727504305
geneviewrs727504305
scholarrs727504305
googlers727504305
pharmgkbrs727504305
gwascentralrs727504305
openSNPrs727504305
23andMers727504305
23andMe allrs727504305
SNP Nexus

SNPshotrs727504305
SNPdbers727504305
MSV3drs727504305
GWAS Ctlgrs727504305
Max Magnitude0
ClinVar
Risk rs727504305(A;A)
Alt rs727504305(A;A)
Reference rs727504305(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.47354525C>T
CLNSRC
CLNACC RCV000154354.1,