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rs730880645

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs730880645(-;-)
Make rs730880645(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342080
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880645
ebirs730880645
HLIrs730880645
Exacrs730880645
Varsomers730880645
Maprs730880645
PheGenIrs730880645
hapmaprs730880645
1000 genomesrs730880645
hgdprs730880645
ensemblrs730880645
gopubmedrs730880645
geneviewrs730880645
scholarrs730880645
googlers730880645
pharmgkbrs730880645
gwascentralrs730880645
openSNPrs730880645
23andMers730880645
23andMe allrs730880645
SNP Nexus

SNPshotrs730880645
SNPdbers730880645
MSV3drs730880645
GWAS Ctlgrs730880645
Max Magnitude0
ClinVar
Risk rs730880645(;)
Alt rs730880645(;)
Reference rs730880645(AG;AG)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47363631_47363632delCT
CLNSRC
CLNACC RCV000151117.2, RCV000158350.2,