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rs876661363

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661363(-;-)
Make rs876661363(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47342094
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs876661363
ebirs876661363
HLIrs876661363
Exacrs876661363
Varsomers876661363
Maprs876661363
PheGenIrs876661363
hapmaprs876661363
1000 genomesrs876661363
hgdprs876661363
ensemblrs876661363
gopubmedrs876661363
geneviewrs876661363
scholarrs876661363
googlers876661363
pharmgkbrs876661363
gwascentralrs876661363
openSNPrs876661363
23andMers876661363
23andMe allrs876661363
SNP Nexus

SNPshotrs876661363
SNPdbers876661363
MSV3drs876661363
GWAS Ctlgrs876661363
Max Magnitude0
ClinVar
Risk rs876661363(;)
Alt rs876661363(;)
Reference rs876661363(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47363645delC
CLNSRC
CLNACC RCV000223887.1,