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rs730880626

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880626(A;A)
Make rs730880626(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47348419
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880626
ebirs730880626
HLIrs730880626
Exacrs730880626
Varsomers730880626
Maprs730880626
PheGenIrs730880626
hapmaprs730880626
1000 genomesrs730880626
hgdprs730880626
ensemblrs730880626
gopubmedrs730880626
geneviewrs730880626
scholarrs730880626
googlers730880626
pharmgkbrs730880626
gwascentralrs730880626
openSNPrs730880626
23andMers730880626
23andMe allrs730880626
SNP Nexus

SNPshotrs730880626
SNPdbers730880626
MSV3drs730880626
GWAS Ctlgrs730880626
Max Magnitude0
ClinVar
Risk rs730880626(A;A)
Alt rs730880626(A;A)
Reference rs730880626(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47369970C>T
CLNSRC
CLNACC RCV000168755.1,