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rs397515900

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515900(C;C)
Make rs397515900(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342869
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515900
ebirs397515900
HLIrs397515900
Exacrs397515900
Varsomers397515900
Maprs397515900
PheGenIrs397515900
hapmaprs397515900
1000 genomesrs397515900
hgdprs397515900
ensemblrs397515900
gopubmedrs397515900
geneviewrs397515900
scholarrs397515900
googlers397515900
pharmgkbrs397515900
gwascentralrs397515900
openSNPrs397515900
23andMers397515900
23andMe allrs397515900
SNP Nexus

SNPshotrs397515900
SNPdbers397515900
MSV3drs397515900
GWAS Ctlgrs397515900
Max Magnitude0
ClinVar
Risk rs397515900(C;C)
Alt rs397515900(C;C)
Reference rs397515900(T;T)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000011.9:g.47364420A>G
CLNSRC
CLNACC RCV000035395.2, RCV000158083.2,