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rs730880362

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880362(-;-)
Make rs730880362(-;GG)
Make rs730880362(GG;GG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351315
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880362
ebirs730880362
HLIrs730880362
Exacrs730880362
Varsomers730880362
Maprs730880362
PheGenIrs730880362
hapmaprs730880362
1000 genomesrs730880362
hgdprs730880362
ensemblrs730880362
gopubmedrs730880362
geneviewrs730880362
scholarrs730880362
googlers730880362
pharmgkbrs730880362
gwascentralrs730880362
openSNPrs730880362
23andMers730880362
23andMe allrs730880362
SNP Nexus

SNPshotrs730880362
SNPdbers730880362
MSV3drs730880362
GWAS Ctlgrs730880362
Max Magnitude0
ClinVar
Risk rs730880362(GG;GG)
Alt rs730880362(GG;GG)
Reference rs730880362(;)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47372867_47372868dupCC
CLNSRC
CLNACC RCV000156329.1,