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rs375471260

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs375471260(C;T)
Make rs375471260(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47351308
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs375471260
ebirs375471260
HLIrs375471260
Exacrs375471260
Varsomers375471260
Maprs375471260
PheGenIrs375471260
hapmaprs375471260
1000 genomesrs375471260
hgdprs375471260
ensemblrs375471260
gopubmedrs375471260
geneviewrs375471260
scholarrs375471260
googlers375471260
pharmgkbrs375471260
gwascentralrs375471260
openSNPrs375471260
23andMers375471260
23andMe allrs375471260
SNP Nexus

SNPshotrs375471260
SNPdbers375471260
MSV3drs375471260
GWAS Ctlgrs375471260
Max Magnitude0
ClinVar
Risk rs375471260(T;T)
Alt rs375471260(T;T)
Reference rs375471260(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified Familial hypertrophic cardiomyopathy 4
Reversed 0
HGVS NC_000011.9:g.47372859C>T
CLNSRC
CLNACC RCV000148688.1, RCV000154385.2, RCV000201432.1,