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rs375774648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs375774648(C;G)
Make rs375774648(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47347666
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs375774648
ebirs375774648
HLIrs375774648
Exacrs375774648
Varsomers375774648
Maprs375774648
PheGenIrs375774648
hapmaprs375774648
1000 genomesrs375774648
hgdprs375774648
ensemblrs375774648
gopubmedrs375774648
geneviewrs375774648
scholarrs375774648
googlers375774648
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gwascentralrs375774648
openSNPrs375774648
23andMers375774648
23andMe allrs375774648
SNP Nexus

SNPshotrs375774648
SNPdbers375774648
MSV3drs375774648
GWAS Ctlgrs375774648
Max Magnitude0
ClinVar
Risk rs375774648(G;G)
Alt rs375774648(G;G)
Reference Rs375774648(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000011.9:g.47369217C>G
CLNSRC Children's Hospital of Eastern Ontario UniProtKB (protein)
CLNACC RCV000035674.3, RCV000154166.3,