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rs727503167

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503167(A;A)
Make rs727503167(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332123
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503167
ebirs727503167
HLIrs727503167
Exacrs727503167
Varsomers727503167
Maprs727503167
PheGenIrs727503167
hapmaprs727503167
1000 genomesrs727503167
hgdprs727503167
ensemblrs727503167
gopubmedrs727503167
geneviewrs727503167
scholarrs727503167
googlers727503167
pharmgkbrs727503167
gwascentralrs727503167
openSNPrs727503167
23andMers727503167
23andMe allrs727503167
SNP Nexus

SNPshotrs727503167
SNPdbers727503167
MSV3drs727503167
GWAS Ctlgrs727503167
Max Magnitude0
ClinVar
Risk rs727503167(A;A)
Alt rs727503167(A;A)
Reference rs727503167(G;G)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353674C>T
CLNSRC
CLNACC RCV000151059.2, RCV000208079.1,