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rs796052199

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052199(A;A)
Make rs796052199(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position92002212
GeneAKAP9
is asnp
is mentioned by
dbSNPrs796052199
ebirs796052199
HLIrs796052199
Exacrs796052199
Varsomers796052199
Maprs796052199
PheGenIrs796052199
hapmaprs796052199
1000 genomesrs796052199
hgdprs796052199
ensemblrs796052199
gopubmedrs796052199
geneviewrs796052199
scholarrs796052199
googlers796052199
pharmgkbrs796052199
gwascentralrs796052199
openSNPrs796052199
23andMers796052199
23andMe allrs796052199
SNP Nexus

SNPshotrs796052199
SNPdbers796052199
MSV3drs796052199
GWAS Ctlgrs796052199
Max Magnitude0
ClinVar
Risk rs796052199(A;A)
Alt rs796052199(A;A)
Reference rs796052199(T;T)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene AKAP9
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000007.13:g.91631526T>A
CLNSRC
CLNACC RCV000190222.1,