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rs730880662

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880662(-;-)
Make rs730880662(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351359
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880662
ebirs730880662
HLIrs730880662
Exacrs730880662
Varsomers730880662
Maprs730880662
PheGenIrs730880662
hapmaprs730880662
1000 genomesrs730880662
hgdprs730880662
ensemblrs730880662
gopubmedrs730880662
geneviewrs730880662
scholarrs730880662
googlers730880662
pharmgkbrs730880662
gwascentralrs730880662
openSNPrs730880662
23andMers730880662
23andMe allrs730880662
SNP Nexus

SNPshotrs730880662
SNPdbers730880662
MSV3drs730880662
GWAS Ctlgrs730880662
Max Magnitude0
ClinVar
Risk rs730880662(;)
Alt rs730880662(;)
Reference rs730880662(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372910delC
CLNSRC
CLNACC RCV000158383.2,