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rs730880568

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880568(A;A)
Make rs730880568(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337459
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880568
ebirs730880568
HLIrs730880568
Exacrs730880568
Varsomers730880568
Maprs730880568
PheGenIrs730880568
hapmaprs730880568
1000 genomesrs730880568
hgdprs730880568
ensemblrs730880568
gopubmedrs730880568
geneviewrs730880568
scholarrs730880568
googlers730880568
pharmgkbrs730880568
gwascentralrs730880568
openSNPrs730880568
23andMers730880568
23andMe allrs730880568
SNP Nexus

SNPshotrs730880568
SNPdbers730880568
MSV3drs730880568
GWAS Ctlgrs730880568
Max Magnitude0
ClinVar
Risk rs730880568(A,C;A,C)
Alt rs730880568(A,C;A,C)
Reference rs730880568(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000011.9:g.47359010C>G; NC_000011.9:g.47359010C>T
CLNSRC
CLNACC RCV000158445.2, RCV000158166.2,