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rs1060501480

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501480(-;-)
Make rs1060501480(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47332221
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs1060501480
dbSNP (old)rs1060501480
ClinGenrs1060501480
ebirs1060501480
HLIrs1060501480
Exacrs1060501480
Gnomadrs1060501480
Varsomers1060501480
Maprs1060501480
PheGenIrs1060501480
Biobankrs1060501480
1000 genomesrs1060501480
hgdprs1060501480
ensemblrs1060501480
gopubmedrs1060501480
geneviewrs1060501480
scholarrs1060501480
googlers1060501480
pharmgkbrs1060501480
gwascentralrs1060501480
openSNPrs1060501480
23andMers1060501480
23andMe allrs1060501480
SNPshotrs1060501480
SNPdbers1060501480
MSV3drs1060501480
GWAS Ctlgrs1060501480
Max Magnitude0
ClinVar
Risk rs1060501480(-;-)
Alt rs1060501480(-;-)
Reference Rs1060501480(G;G)
Significance Pathogenic
Disease Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353772delC
CLNSRC
CLNACC RCV000460163.1,