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rs876661368

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661368(A;A)
Make rs876661368(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47347650
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs876661368
ebirs876661368
HLIrs876661368
Exacrs876661368
Varsomers876661368
Maprs876661368
PheGenIrs876661368
hapmaprs876661368
1000 genomesrs876661368
hgdprs876661368
ensemblrs876661368
gopubmedrs876661368
geneviewrs876661368
scholarrs876661368
googlers876661368
pharmgkbrs876661368
gwascentralrs876661368
openSNPrs876661368
23andMers876661368
23andMe allrs876661368
SNP Nexus

SNPshotrs876661368
SNPdbers876661368
MSV3drs876661368
GWAS Ctlgrs876661368
Max Magnitude0
ClinVar
Risk rs876661368(A;A)
Alt rs876661368(A;A)
Reference rs876661368(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47369201C>T
CLNSRC
CLNACC RCV000223732.1,