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

rs786205470

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205470(C;C)
Make rs786205470(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47332582
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs786205470
ebirs786205470
HLIrs786205470
Exacrs786205470
Varsomers786205470
Maprs786205470
PheGenIrs786205470
hapmaprs786205470
1000 genomesrs786205470
hgdprs786205470
ensemblrs786205470
gopubmedrs786205470
geneviewrs786205470
scholarrs786205470
googlers786205470
pharmgkbrs786205470
gwascentralrs786205470
openSNPrs786205470
23andMers786205470
23andMe allrs786205470
SNP Nexus

SNPshotrs786205470
SNPdbers786205470
MSV3drs786205470
GWAS Ctlgrs786205470
Max Magnitude0
ClinVar
Risk rs786205470(C;C)
Alt rs786205470(C;C)
Reference rs786205470(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354133A>G
CLNSRC
CLNACC RCV000171195.1,