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rs11570077

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11570077(C;C)
Make rs11570077(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343568
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs11570077
ebirs11570077
HLIrs11570077
Exacrs11570077
Varsomers11570077
Maprs11570077
PheGenIrs11570077
hapmaprs11570077
1000 genomesrs11570077
hgdprs11570077
ensemblrs11570077
gopubmedrs11570077
geneviewrs11570077
scholarrs11570077
googlers11570077
pharmgkbrs11570077
gwascentralrs11570077
openSNPrs11570077
23andMers11570077
23andMe allrs11570077
SNP Nexus

SNPshotrs11570077
SNPdbers11570077
MSV3drs11570077
GWAS Ctlgrs11570077
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs11570077(C;C)
Alt rs11570077(C;C)
Reference rs11570077(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47365119G>C
CLNSRC
CLNACC RCV000158334.2,