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rs730880534

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880534(A;A)
Make rs730880534(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343084
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880534
ebirs730880534
HLIrs730880534
Exacrs730880534
Varsomers730880534
Maprs730880534
PheGenIrs730880534
hapmaprs730880534
1000 genomesrs730880534
hgdprs730880534
ensemblrs730880534
gopubmedrs730880534
geneviewrs730880534
scholarrs730880534
googlers730880534
pharmgkbrs730880534
gwascentralrs730880534
openSNPrs730880534
23andMers730880534
23andMe allrs730880534
SNP Nexus

SNPshotrs730880534
SNPdbers730880534
MSV3drs730880534
GWAS Ctlgrs730880534
Max Magnitude0
ClinVar
Risk rs730880534(A;A)
Alt rs730880534(A;A)
Reference rs730880534(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364635C>T
CLNSRC
CLNACC RCV000158074.1,