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rs730880629

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880629(A;T)
Make rs730880629(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47347430
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880629
ebirs730880629
HLIrs730880629
Exacrs730880629
Varsomers730880629
Maprs730880629
PheGenIrs730880629
hapmaprs730880629
1000 genomesrs730880629
hgdprs730880629
ensemblrs730880629
gopubmedrs730880629
geneviewrs730880629
scholarrs730880629
googlers730880629
pharmgkbrs730880629
gwascentralrs730880629
openSNPrs730880629
23andMers730880629
23andMe allrs730880629
SNP Nexus

SNPshotrs730880629
SNPdbers730880629
MSV3drs730880629
GWAS Ctlgrs730880629
Max Magnitude0
ClinVar
Risk rs730880629(T;T)
Alt rs730880629(T;T)
Reference rs730880629(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47368981T>A
CLNSRC
CLNACC RCV000158318.2,