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rs730880580

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880580(A;A)
Make rs730880580(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351301
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880580
ebirs730880580
HLIrs730880580
Exacrs730880580
Varsomers730880580
Maprs730880580
PheGenIrs730880580
hapmaprs730880580
1000 genomesrs730880580
hgdprs730880580
ensemblrs730880580
gopubmedrs730880580
geneviewrs730880580
scholarrs730880580
googlers730880580
pharmgkbrs730880580
gwascentralrs730880580
openSNPrs730880580
23andMers730880580
23andMe allrs730880580
SNP Nexus

SNPshotrs730880580
SNPdbers730880580
MSV3drs730880580
GWAS Ctlgrs730880580
Max Magnitude0
ClinVar
Risk rs730880580(A;A)
Alt rs730880580(A;A)
Reference rs730880580(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372852C>T
CLNSRC
CLNACC RCV000158199.1,