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rs730880690

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880690(C;C)
Make rs730880690(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342575
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880690
ebirs730880690
HLIrs730880690
Exacrs730880690
Varsomers730880690
Maprs730880690
PheGenIrs730880690
hapmaprs730880690
1000 genomesrs730880690
hgdprs730880690
ensemblrs730880690
gopubmedrs730880690
geneviewrs730880690
scholarrs730880690
googlers730880690
pharmgkbrs730880690
gwascentralrs730880690
openSNPrs730880690
23andMers730880690
23andMe allrs730880690
SNP Nexus

SNPshotrs730880690
SNPdbers730880690
MSV3drs730880690
GWAS Ctlgrs730880690
Max Magnitude0
ClinVar
Risk rs730880690(C;C)
Alt rs730880690(C;C)
Reference rs730880690(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364126C>G
CLNSRC
CLNACC RCV000158431.1,