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rs397516015

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516015(A;C)
Make rs397516015(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333201
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516015
ebirs397516015
HLIrs397516015
Exacrs397516015
Varsomers397516015
Maprs397516015
PheGenIrs397516015
hapmaprs397516015
1000 genomesrs397516015
hgdprs397516015
ensemblrs397516015
gopubmedrs397516015
geneviewrs397516015
scholarrs397516015
googlers397516015
pharmgkbrs397516015
gwascentralrs397516015
openSNPrs397516015
23andMers397516015
23andMe allrs397516015
SNP Nexus

SNPshotrs397516015
SNPdbers397516015
MSV3drs397516015
GWAS Ctlgrs397516015
Max Magnitude0
ClinVar
Risk rs397516015(C;C)
Alt rs397516015(C;C)
Reference rs397516015(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000011.9:g.47354752T>G
CLNSRC
CLNACC RCV000035578.3, RCV000158227.1,