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rs876657705

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657705(-;-)
Make rs876657705(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47335158
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs876657705
ebirs876657705
HLIrs876657705
Exacrs876657705
Varsomers876657705
Maprs876657705
PheGenIrs876657705
hapmaprs876657705
1000 genomesrs876657705
hgdprs876657705
ensemblrs876657705
gopubmedrs876657705
geneviewrs876657705
scholarrs876657705
googlers876657705
pharmgkbrs876657705
gwascentralrs876657705
openSNPrs876657705
23andMers876657705
23andMe allrs876657705
SNP Nexus

SNPshotrs876657705
SNPdbers876657705
MSV3drs876657705
GWAS Ctlgrs876657705
Max Magnitude0
ClinVar
Risk rs876657705(;)
Alt rs876657705(;)
Reference rs876657705(T;T)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47356709delA
CLNSRC
CLNACC RCV000217959.1,