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rs730880703

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880703(C;G)
Make rs730880703(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350109
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880703
ebirs730880703
HLIrs730880703
Exacrs730880703
Varsomers730880703
Maprs730880703
PheGenIrs730880703
hapmaprs730880703
1000 genomesrs730880703
hgdprs730880703
ensemblrs730880703
gopubmedrs730880703
geneviewrs730880703
scholarrs730880703
googlers730880703
pharmgkbrs730880703
gwascentralrs730880703
openSNPrs730880703
23andMers730880703
23andMe allrs730880703
SNP Nexus

SNPshotrs730880703
SNPdbers730880703
MSV3drs730880703
GWAS Ctlgrs730880703
Max Magnitude0
ClinVar
Risk rs730880703(G;G)
Alt rs730880703(G;G)
Reference rs730880703(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47371660G>C
CLNSRC
CLNACC RCV000158462.1,