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rs397515995

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GACCA;GACCA) 0 common in clinvar
Make rs397515995(-;-)
Make rs397515995(-;GACCA)
ReferenceGRCh38 38.1/141
Chromosome11
Position47333969
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515995
ebirs397515995
HLIrs397515995
Exacrs397515995
Varsomers397515995
Maprs397515995
PheGenIrs397515995
hapmaprs397515995
1000 genomesrs397515995
hgdprs397515995
ensemblrs397515995
gopubmedrs397515995
geneviewrs397515995
scholarrs397515995
googlers397515995
pharmgkbrs397515995
gwascentralrs397515995
openSNPrs397515995
23andMers397515995
23andMe allrs397515995
SNP Nexus

SNPshotrs397515995
SNPdbers397515995
MSV3drs397515995
GWAS Ctlgrs397515995
Max Magnitude0
ClinVar
Risk rs397515995(;)
Alt rs397515995(;)
Reference rs397515995(GACCA;GACCA)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355520_47355524delTGGTC
CLNSRC ClinVar
CLNACC RCV000035544.2,