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rs730880532

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880532(A;G)
Make rs730880532(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343134
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880532
ebirs730880532
HLIrs730880532
Exacrs730880532
Varsomers730880532
Maprs730880532
PheGenIrs730880532
hapmaprs730880532
1000 genomesrs730880532
hgdprs730880532
ensemblrs730880532
gopubmedrs730880532
geneviewrs730880532
scholarrs730880532
googlers730880532
pharmgkbrs730880532
gwascentralrs730880532
openSNPrs730880532
23andMers730880532
23andMe allrs730880532
SNP Nexus

SNPshotrs730880532
SNPdbers730880532
MSV3drs730880532
GWAS Ctlgrs730880532
Max Magnitude0
ClinVar
Risk rs730880532(G;G)
Alt rs730880532(G;G)
Reference rs730880532(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47364685T>C
CLNSRC
CLNACC RCV000158069.2, RCV000223683.1,