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rs730880652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;ATGCG) 6.2 Familial Hypertrophic Cardiomyopathy
(ATGCG;ATGCG) 0 common in clinvar


Make rs730880652(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337534
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880652
dbSNP (classic)rs730880652
ClinGenrs730880652
ebirs730880652
HLIrs730880652
Exacrs730880652
Gnomadrs730880652
Varsomers730880652
LitVarrs730880652
Maprs730880652
PheGenIrs730880652
Biobankrs730880652
1000 genomesrs730880652
hgdprs730880652
ensemblrs730880652
geneviewrs730880652
scholarrs730880652
googlers730880652
pharmgkbrs730880652
gwascentralrs730880652
openSNPrs730880652
23andMers730880652
SNPshotrs730880652
SNPdbers730880652
MSV3drs730880652
GWAS Ctlgrs730880652
Max Magnitude6.2
ClinVar
Risk rs730880652(-;-)
Alt rs730880652(-;-)
Reference Rs730880652(ATGCG;ATGCG)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359085_47359089delCGCAT
CLNSRC
CLNACC RCV000158364.3,