Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880701

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880701(A;A)
Make rs730880701(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333726
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880701
ebirs730880701
HLIrs730880701
Exacrs730880701
Varsomers730880701
Maprs730880701
PheGenIrs730880701
hapmaprs730880701
1000 genomesrs730880701
hgdprs730880701
ensemblrs730880701
gopubmedrs730880701
geneviewrs730880701
scholarrs730880701
googlers730880701
pharmgkbrs730880701
gwascentralrs730880701
openSNPrs730880701
23andMers730880701
23andMe allrs730880701
SNP Nexus

SNPshotrs730880701
SNPdbers730880701
MSV3drs730880701
GWAS Ctlgrs730880701
Max Magnitude0
ClinVar
Risk rs730880701(A;A)
Alt rs730880701(A;A)
Reference rs730880701(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47355277C>T
CLNSRC
CLNACC RCV000158455.1,