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rs730880693

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880693(A;A)
Make rs730880693(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342112
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880693
ebirs730880693
HLIrs730880693
Exacrs730880693
Varsomers730880693
Maprs730880693
PheGenIrs730880693
hapmaprs730880693
1000 genomesrs730880693
hgdprs730880693
ensemblrs730880693
gopubmedrs730880693
geneviewrs730880693
scholarrs730880693
googlers730880693
pharmgkbrs730880693
gwascentralrs730880693
openSNPrs730880693
23andMers730880693
23andMe allrs730880693
SNP Nexus

SNPshotrs730880693
SNPdbers730880693
MSV3drs730880693
GWAS Ctlgrs730880693
Max Magnitude0
ClinVar
Risk rs730880693(A;A)
Alt rs730880693(A;A)
Reference rs730880693(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47363663C>T
CLNSRC
CLNACC RCV000158435.1,