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rs397515925

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGAGGGCACAC;AGAGGGCACAC) 0 common in clinvar
Make rs397515925(-;-)
Make rs397515925(-;AGAGGGCACAC)
ReferenceGRCh38 38.1/141
Chromosome11
Position47351344
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515925
ebirs397515925
HLIrs397515925
Exacrs397515925
Varsomers397515925
Maprs397515925
PheGenIrs397515925
hapmaprs397515925
1000 genomesrs397515925
hgdprs397515925
ensemblrs397515925
gopubmedrs397515925
geneviewrs397515925
scholarrs397515925
googlers397515925
pharmgkbrs397515925
gwascentralrs397515925
openSNPrs397515925
23andMers397515925
23andMe allrs397515925
SNP Nexus

SNPshotrs397515925
SNPdbers397515925
MSV3drs397515925
GWAS Ctlgrs397515925
Max Magnitude0
ClinVar
Risk rs397515925(;)
Alt rs397515925(;)
Reference rs397515925(AGAGGGCACAC;AGAGGGCACAC)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 4 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47372895_47372905delGTGTGCCCTCT
CLNSRC ClinVar
CLNACC RCV000035432.4, RCV000158384.2, RCV000211800.1,