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rs876657706

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657706(-;-)
Make rs876657706(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47332681
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs876657706
ebirs876657706
HLIrs876657706
Exacrs876657706
Varsomers876657706
Maprs876657706
PheGenIrs876657706
hapmaprs876657706
1000 genomesrs876657706
hgdprs876657706
ensemblrs876657706
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geneviewrs876657706
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openSNPrs876657706
23andMers876657706
23andMe allrs876657706
SNP Nexus

SNPshotrs876657706
SNPdbers876657706
MSV3drs876657706
GWAS Ctlgrs876657706
Max Magnitude0
ClinVar
Risk rs876657706(;)
Alt rs876657706(;)
Reference rs876657706(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354232delT
CLNSRC
CLNACC RCV000215999.1,