Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052198

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052198(C;C)
Make rs796052198(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position113356741
GeneANK2
is asnp
is mentioned by
dbSNPrs796052198
ebirs796052198
HLIrs796052198
Exacrs796052198
Varsomers796052198
Maprs796052198
PheGenIrs796052198
hapmaprs796052198
1000 genomesrs796052198
hgdprs796052198
ensemblrs796052198
gopubmedrs796052198
geneviewrs796052198
scholarrs796052198
googlers796052198
pharmgkbrs796052198
gwascentralrs796052198
openSNPrs796052198
23andMers796052198
23andMe allrs796052198
SNP Nexus

SNPshotrs796052198
SNPdbers796052198
MSV3drs796052198
GWAS Ctlgrs796052198
Max Magnitude0
ClinVar
Risk rs796052198(C;C)
Alt rs796052198(C;C)
Reference rs796052198(T;T)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene ANK2
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114277897T>C
CLNSRC
CLNACC RCV000190221.1,