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rs876657703

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657703(-;-)
Make rs876657703(-;G)
Make rs876657703(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47342842
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs876657703
ebirs876657703
HLIrs876657703
Exacrs876657703
Varsomers876657703
Maprs876657703
PheGenIrs876657703
hapmaprs876657703
1000 genomesrs876657703
hgdprs876657703
ensemblrs876657703
gopubmedrs876657703
geneviewrs876657703
scholarrs876657703
googlers876657703
pharmgkbrs876657703
gwascentralrs876657703
openSNPrs876657703
23andMers876657703
23andMe allrs876657703
SNP Nexus

SNPshotrs876657703
SNPdbers876657703
MSV3drs876657703
GWAS Ctlgrs876657703
Max Magnitude0
ClinVar
Risk rs876657703(G;G)
Alt rs876657703(G;G)
Reference rs876657703(;)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364394dupC
CLNSRC
CLNACC RCV000222228.1,