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rs730880579

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880579(A;T)
Make rs730880579(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335050
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880579
ebirs730880579
HLIrs730880579
Exacrs730880579
Varsomers730880579
Maprs730880579
PheGenIrs730880579
hapmaprs730880579
1000 genomesrs730880579
hgdprs730880579
ensemblrs730880579
gopubmedrs730880579
geneviewrs730880579
scholarrs730880579
googlers730880579
pharmgkbrs730880579
gwascentralrs730880579
openSNPrs730880579
23andMers730880579
23andMe allrs730880579
SNP Nexus

SNPshotrs730880579
SNPdbers730880579
MSV3drs730880579
GWAS Ctlgrs730880579
Max Magnitude0
ClinVar
Risk rs730880579(T;T)
Alt rs730880579(T;T)
Reference rs730880579(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47356601T>A
CLNSRC
CLNACC RCV000158194.2,