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rs730880337

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880337(-;-)
Make rs730880337(-;AGTG)
Make rs730880337(AGTG;AGTG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332968
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880337
ebirs730880337
HLIrs730880337
Exacrs730880337
Varsomers730880337
Maprs730880337
PheGenIrs730880337
hapmaprs730880337
1000 genomesrs730880337
hgdprs730880337
ensemblrs730880337
gopubmedrs730880337
geneviewrs730880337
scholarrs730880337
googlers730880337
pharmgkbrs730880337
gwascentralrs730880337
openSNPrs730880337
23andMers730880337
23andMe allrs730880337
SNP Nexus

SNPshotrs730880337
SNPdbers730880337
MSV3drs730880337
GWAS Ctlgrs730880337
Max Magnitude0
ClinVar
Risk rs730880337(AGTG;AGTG)
Alt rs730880337(AGTG;AGTG)
Reference rs730880337(;)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354520_47354523dupCACT
CLNSRC
CLNACC RCV000154325.2,