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rs730880631

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880631(C;T)
Make rs730880631(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346282
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880631
ebirs730880631
HLIrs730880631
Exacrs730880631
Varsomers730880631
Maprs730880631
PheGenIrs730880631
hapmaprs730880631
1000 genomesrs730880631
hgdprs730880631
ensemblrs730880631
gopubmedrs730880631
geneviewrs730880631
scholarrs730880631
googlers730880631
pharmgkbrs730880631
gwascentralrs730880631
openSNPrs730880631
23andMers730880631
23andMe allrs730880631
SNP Nexus

SNPshotrs730880631
SNPdbers730880631
MSV3drs730880631
GWAS Ctlgrs730880631
Max Magnitude0
ClinVar
Risk rs730880631(T;T)
Alt rs730880631(T;T)
Reference rs730880631(C;C)
Significance Other
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47367833G>A
CLNSRC
CLNACC RCV000158327.2,