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rs730880592

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880592(A;A)
Make rs730880592(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332705
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880592
ebirs730880592
HLIrs730880592
Exacrs730880592
Varsomers730880592
Maprs730880592
PheGenIrs730880592
hapmaprs730880592
1000 genomesrs730880592
hgdprs730880592
ensemblrs730880592
gopubmedrs730880592
geneviewrs730880592
scholarrs730880592
googlers730880592
pharmgkbrs730880592
gwascentralrs730880592
openSNPrs730880592
23andMers730880592
23andMe allrs730880592
SNP Nexus

SNPshotrs730880592
SNPdbers730880592
MSV3drs730880592
GWAS Ctlgrs730880592
Max Magnitude0
ClinVar
Risk rs730880592(A,G;A,G)
Alt rs730880592(A,G;A,G)
Reference rs730880592(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354256G>C; NC_000011.9:g.47354256G>T
CLNSRC
CLNACC RCV000158240.2, RCV000158239.1,