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rs730880544

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6.2 Familial Hypertrophic Cardiomyopathy
Make rs730880544(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342680
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880544
dbSNP (classic)rs730880544
ClinGenrs730880544
ebirs730880544
HLIrs730880544
Exacrs730880544
Gnomadrs730880544
Varsomers730880544
LitVarrs730880544
Maprs730880544
PheGenIrs730880544
Biobankrs730880544
1000 genomesrs730880544
hgdprs730880544
ensemblrs730880544
geneviewrs730880544
scholarrs730880544
googlers730880544
pharmgkbrs730880544
gwascentralrs730880544
openSNPrs730880544
23andMers730880544
SNPshotrs730880544
SNPdbers730880544
MSV3drs730880544
GWAS Ctlgrs730880544
Max Magnitude6.2
ClinVar
Risk rs730880544(T;T)
Alt rs730880544(T;T)
Reference Rs730880544(C;C)
Significance Other
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364231G>A
CLNSRC
CLNACC RCV000158098.2,