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rs730880609

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880609(A;A)
Make rs730880609(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332072
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880609
ebirs730880609
HLIrs730880609
Exacrs730880609
Varsomers730880609
Maprs730880609
PheGenIrs730880609
hapmaprs730880609
1000 genomesrs730880609
hgdprs730880609
ensemblrs730880609
gopubmedrs730880609
geneviewrs730880609
scholarrs730880609
googlers730880609
pharmgkbrs730880609
gwascentralrs730880609
openSNPrs730880609
23andMers730880609
23andMe allrs730880609
SNP Nexus

SNPshotrs730880609
SNPdbers730880609
MSV3drs730880609
GWAS Ctlgrs730880609
Max Magnitude0
ClinVar
Risk rs730880609(A;A)
Alt rs730880609(A;A)
Reference rs730880609(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47353623C>T
CLNSRC
CLNACC RCV000158272.1,