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rs876661365

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661365(-;-)
Make rs876661365(-;A)
Make rs876661365(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47335077
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs876661365
ebirs876661365
HLIrs876661365
Exacrs876661365
Varsomers876661365
Maprs876661365
PheGenIrs876661365
hapmaprs876661365
1000 genomesrs876661365
hgdprs876661365
ensemblrs876661365
gopubmedrs876661365
geneviewrs876661365
scholarrs876661365
googlers876661365
pharmgkbrs876661365
gwascentralrs876661365
openSNPrs876661365
23andMers876661365
23andMe allrs876661365
SNP Nexus

SNPshotrs876661365
SNPdbers876661365
MSV3drs876661365
GWAS Ctlgrs876661365
Max Magnitude0
ClinVar
Risk rs876661365(A;A)
Alt rs876661365(A;A)
Reference rs876661365(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47356629dupT
CLNSRC
CLNACC RCV000223915.1,