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rs730880663

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880663(-;-)
Make rs730880663(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351349
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880663
ebirs730880663
HLIrs730880663
Exacrs730880663
Varsomers730880663
Maprs730880663
PheGenIrs730880663
hapmaprs730880663
1000 genomesrs730880663
hgdprs730880663
ensemblrs730880663
gopubmedrs730880663
geneviewrs730880663
scholarrs730880663
googlers730880663
pharmgkbrs730880663
gwascentralrs730880663
openSNPrs730880663
23andMers730880663
23andMe allrs730880663
SNP Nexus

SNPshotrs730880663
SNPdbers730880663
MSV3drs730880663
GWAS Ctlgrs730880663
Max Magnitude0
ClinVar
Risk rs730880663(;)
Alt rs730880663(;)
Reference rs730880663(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372900delC
CLNSRC
CLNACC RCV000158385.1,