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rs121908566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908566(C;T)
Make rs121908566(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position92040690
GeneAKAP9
is asnp
is mentioned by
dbSNPrs121908566
ebirs121908566
HLIrs121908566
Exacrs121908566
Varsomers121908566
Maprs121908566
PheGenIrs121908566
hapmaprs121908566
1000 genomesrs121908566
hgdprs121908566
ensemblrs121908566
gopubmedrs121908566
geneviewrs121908566
scholarrs121908566
googlers121908566
pharmgkbrs121908566
gwascentralrs121908566
openSNPrs121908566
23andMers121908566
23andMe allrs121908566
SNP Nexus

SNPshotrs121908566
SNPdbers121908566
MSV3drs121908566
GWAS Ctlgrs121908566
Max Magnitude0
OMIM604001
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908566(T;T)
Alt rs121908566(T;T)
Reference rs121908566(C;C)
Significance Pathogenic
Disease Long QT syndrome 11
Variation info
Gene AKAP9
CLNDBN Long QT syndrome 11
Reversed 0
HGVS NC_000007.13:g.91670004C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006241.3,