Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880707

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880707(A;G)
Make rs730880707(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349775
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880707
ebirs730880707
HLIrs730880707
Exacrs730880707
Varsomers730880707
Maprs730880707
PheGenIrs730880707
hapmaprs730880707
1000 genomesrs730880707
hgdprs730880707
ensemblrs730880707
gopubmedrs730880707
geneviewrs730880707
scholarrs730880707
googlers730880707
pharmgkbrs730880707
gwascentralrs730880707
openSNPrs730880707
23andMers730880707
23andMe allrs730880707
SNP Nexus

SNPshotrs730880707
SNPdbers730880707
MSV3drs730880707
GWAS Ctlgrs730880707
Max Magnitude0
ClinVar
Risk rs730880707(G;G)
Alt rs730880707(G;G)
Reference rs730880707(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47371326T>C
CLNSRC
CLNACC RCV000158468.2,