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

rs730880571

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880571(A;A)
Make rs730880571(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337442
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880571
ebirs730880571
HLIrs730880571
Exacrs730880571
Varsomers730880571
Maprs730880571
PheGenIrs730880571
hapmaprs730880571
1000 genomesrs730880571
hgdprs730880571
ensemblrs730880571
gopubmedrs730880571
geneviewrs730880571
scholarrs730880571
googlers730880571
pharmgkbrs730880571
gwascentralrs730880571
openSNPrs730880571
23andMers730880571
23andMe allrs730880571
SNP Nexus

SNPshotrs730880571
SNPdbers730880571
MSV3drs730880571
GWAS Ctlgrs730880571
Max Magnitude0
ClinVar
Risk rs730880571(A;A)
Alt rs730880571(A;A)
Reference rs730880571(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47358993C>T
CLNSRC
CLNACC RCV000158171.2,