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rs397516038

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516038(-;-)
Make rs397516038(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position47332151
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516038
ebirs397516038
HLIrs397516038
Exacrs397516038
Varsomers397516038
Maprs397516038
PheGenIrs397516038
hapmaprs397516038
1000 genomesrs397516038
hgdprs397516038
ensemblrs397516038
gopubmedrs397516038
geneviewrs397516038
scholarrs397516038
googlers397516038
pharmgkbrs397516038
gwascentralrs397516038
openSNPrs397516038
23andMers397516038
23andMe allrs397516038
SNP Nexus

SNPshotrs397516038
SNPdbers397516038
MSV3drs397516038
GWAS Ctlgrs397516038
Max Magnitude0
ClinVar
Risk rs397516038(;)
Alt rs397516038(;)
Reference rs397516038(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353702delG
CLNSRC ClinVar
CLNACC RCV000035612.3,