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rs796052197

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052197(C;C)
Make rs796052197(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position113354767
GeneANK2
is asnp
is mentioned by
dbSNPrs796052197
ebirs796052197
HLIrs796052197
Exacrs796052197
Varsomers796052197
Maprs796052197
PheGenIrs796052197
hapmaprs796052197
1000 genomesrs796052197
hgdprs796052197
ensemblrs796052197
gopubmedrs796052197
geneviewrs796052197
scholarrs796052197
googlers796052197
pharmgkbrs796052197
gwascentralrs796052197
openSNPrs796052197
23andMers796052197
23andMe allrs796052197
SNP Nexus

SNPshotrs796052197
SNPdbers796052197
MSV3drs796052197
GWAS Ctlgrs796052197
Max Magnitude0
ClinVar
Risk rs796052197(C;C)
Alt rs796052197(C;C)
Reference rs796052197(T;T)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene ANK2
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114275923T>C
CLNSRC
CLNACC RCV000190220.1,