Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060501484

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501484(-;-)
Make rs1060501484(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47332576
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs1060501484
dbSNP (classic)rs1060501484
ClinGenrs1060501484
ebirs1060501484
HLIrs1060501484
Exacrs1060501484
Gnomadrs1060501484
Varsomers1060501484
LitVarrs1060501484
Maprs1060501484
PheGenIrs1060501484
Biobankrs1060501484
1000 genomesrs1060501484
hgdprs1060501484
ensemblrs1060501484
geneviewrs1060501484
scholarrs1060501484
googlers1060501484
pharmgkbrs1060501484
gwascentralrs1060501484
openSNPrs1060501484
23andMers1060501484
SNPshotrs1060501484
SNPdbers1060501484
MSV3drs1060501484
GWAS Ctlgrs1060501484
Max Magnitude0
ClinVar
Risk rs1060501484(-;-)
Alt rs1060501484(-;-)
Reference Rs1060501484(G;G)
Significance Pathogenic
Disease Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354127delC
CLNSRC
CLNACC RCV000460566.1,