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rs730880595

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880595(G;T)
Make rs730880595(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332609
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880595
ebirs730880595
HLIrs730880595
Exacrs730880595
Varsomers730880595
Maprs730880595
PheGenIrs730880595
hapmaprs730880595
1000 genomesrs730880595
hgdprs730880595
ensemblrs730880595
gopubmedrs730880595
geneviewrs730880595
scholarrs730880595
googlers730880595
pharmgkbrs730880595
gwascentralrs730880595
openSNPrs730880595
23andMers730880595
23andMe allrs730880595
SNP Nexus

SNPshotrs730880595
SNPdbers730880595
MSV3drs730880595
GWAS Ctlgrs730880595
Max Magnitude0
ClinVar
Risk rs730880595(T;T)
Alt rs730880595(T;T)
Reference rs730880595(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47354160C>A
CLNSRC
CLNACC RCV000158245.1, RCV000223819.1,