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rs730880639

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880639(A;A)
Make rs730880639(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343491
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880639
ebirs730880639
HLIrs730880639
Exacrs730880639
Varsomers730880639
Maprs730880639
PheGenIrs730880639
hapmaprs730880639
1000 genomesrs730880639
hgdprs730880639
ensemblrs730880639
gopubmedrs730880639
geneviewrs730880639
scholarrs730880639
googlers730880639
pharmgkbrs730880639
gwascentralrs730880639
openSNPrs730880639
23andMers730880639
23andMe allrs730880639
SNP Nexus

SNPshotrs730880639
SNPdbers730880639
MSV3drs730880639
GWAS Ctlgrs730880639
Max Magnitude0
ClinVar
Risk rs730880639(A;A)
Alt rs730880639(A;A)
Reference rs730880639(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47365042C>T
CLNSRC
CLNACC RCV000158340.2,