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rs397516086

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516086(A;A)
Make rs397516086(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346303
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516086
ebirs397516086
HLIrs397516086
Exacrs397516086
Varsomers397516086
Maprs397516086
PheGenIrs397516086
hapmaprs397516086
1000 genomesrs397516086
hgdprs397516086
ensemblrs397516086
gopubmedrs397516086
geneviewrs397516086
scholarrs397516086
googlers397516086
pharmgkbrs397516086
gwascentralrs397516086
openSNPrs397516086
23andMers397516086
23andMe allrs397516086
SNP Nexus

SNPshotrs397516086
SNPdbers397516086
MSV3drs397516086
GWAS Ctlgrs397516086
Max Magnitude0
ClinVar
Risk rs397516086(A;A)
Alt rs397516086(A;A)
Reference rs397516086(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000011.9:g.47367854C>T
CLNSRC
CLNACC RCV000035691.2, RCV000158324.1,