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rs371061770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371061770(A;A)
Make rs371061770(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position47333610
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs371061770
ebirs371061770
HLIrs371061770
Exacrs371061770
Varsomers371061770
Maprs371061770
PheGenIrs371061770
hapmaprs371061770
1000 genomesrs371061770
hgdprs371061770
ensemblrs371061770
gopubmedrs371061770
geneviewrs371061770
scholarrs371061770
googlers371061770
pharmgkbrs371061770
gwascentralrs371061770
openSNPrs371061770
23andMers371061770
23andMe allrs371061770
SNP Nexus

SNPshotrs371061770
SNPdbers371061770
MSV3drs371061770
GWAS Ctlgrs371061770
Max Magnitude0
ClinVar
Risk rs371061770(A;A)
Alt rs371061770(A;A)
Reference rs371061770(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47355161G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000148658.1, RCV000158217.2, RCV000168305.1,