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rs796052200

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052200(A;A)
Make rs796052200(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position92045186
GeneAKAP9
is asnp
is mentioned by
dbSNPrs796052200
ebirs796052200
HLIrs796052200
Exacrs796052200
Varsomers796052200
Maprs796052200
PheGenIrs796052200
hapmaprs796052200
1000 genomesrs796052200
hgdprs796052200
ensemblrs796052200
gopubmedrs796052200
geneviewrs796052200
scholarrs796052200
googlers796052200
pharmgkbrs796052200
gwascentralrs796052200
openSNPrs796052200
23andMers796052200
23andMe allrs796052200
SNP Nexus

SNPshotrs796052200
SNPdbers796052200
MSV3drs796052200
GWAS Ctlgrs796052200
Max Magnitude0
ClinVar
Risk rs796052200(A;A)
Alt rs796052200(A;A)
Reference rs796052200(T;T)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene AKAP9
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000007.13:g.91674500T>A
CLNSRC
CLNACC RCV000190223.1,