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rs730880633

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880633(A;G)
Make rs730880633(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346213
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880633
ebirs730880633
HLIrs730880633
Exacrs730880633
Varsomers730880633
Maprs730880633
PheGenIrs730880633
hapmaprs730880633
1000 genomesrs730880633
hgdprs730880633
ensemblrs730880633
gopubmedrs730880633
geneviewrs730880633
scholarrs730880633
googlers730880633
pharmgkbrs730880633
gwascentralrs730880633
openSNPrs730880633
23andMers730880633
23andMe allrs730880633
SNP Nexus

SNPshotrs730880633
SNPdbers730880633
MSV3drs730880633
GWAS Ctlgrs730880633
Max Magnitude0
ClinVar
Risk rs730880633(G;G)
Alt rs730880633(G;G)
Reference rs730880633(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47367764T>C
CLNSRC
CLNACC RCV000158330.1,