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rs730880700

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880700(A;A)
Make rs730880700(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351293
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880700
ebirs730880700
HLIrs730880700
Exacrs730880700
Varsomers730880700
Maprs730880700
PheGenIrs730880700
hapmaprs730880700
1000 genomesrs730880700
hgdprs730880700
ensemblrs730880700
gopubmedrs730880700
geneviewrs730880700
scholarrs730880700
googlers730880700
pharmgkbrs730880700
gwascentralrs730880700
openSNPrs730880700
23andMers730880700
23andMe allrs730880700
SNP Nexus

SNPshotrs730880700
SNPdbers730880700
MSV3drs730880700
GWAS Ctlgrs730880700
Max Magnitude0
ClinVar
Risk rs730880700(A;A)
Alt rs730880700(A;A)
Reference rs730880700(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47372844C>T
CLNSRC
CLNACC RCV000158454.2,