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rs730880684

From SNPedia

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


Make rs730880684(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47347447
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880684
dbSNP (classic)rs730880684
ClinGenrs730880684
ebirs730880684
HLIrs730880684
Exacrs730880684
Gnomadrs730880684
Varsomers730880684
LitVarrs730880684
Maprs730880684
PheGenIrs730880684
Biobankrs730880684
1000 genomesrs730880684
hgdprs730880684
ensemblrs730880684
geneviewrs730880684
scholarrs730880684
googlers730880684
pharmgkbrs730880684
gwascentralrs730880684
openSNPrs730880684
23andMers730880684
SNPshotrs730880684
SNPdbers730880684
MSV3drs730880684
GWAS Ctlgrs730880684
Max Magnitude6.2
ClinVar
Risk rs730880684(-;-)
Alt rs730880684(-;-)
Reference Rs730880684(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47368998delA
CLNSRC
CLNACC RCV000158420.2,