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rs755287627

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs755287627(A;G)
Make rs755287627(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position113353494
GeneANK2
is asnp
is mentioned by
dbSNPrs755287627
ebirs755287627
HLIrs755287627
Exacrs755287627
Varsomers755287627
Maprs755287627
PheGenIrs755287627
hapmaprs755287627
1000 genomesrs755287627
hgdprs755287627
ensemblrs755287627
gopubmedrs755287627
geneviewrs755287627
scholarrs755287627
googlers755287627
pharmgkbrs755287627
gwascentralrs755287627
openSNPrs755287627
23andMers755287627
23andMe allrs755287627
SNP Nexus

SNPshotrs755287627
SNPdbers755287627
MSV3drs755287627
GWAS Ctlgrs755287627
Max Magnitude0
ClinVar
Risk rs755287627(G;G)
Alt rs755287627(G;G)
Reference rs755287627(A;A)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene ANK2
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114274650A>G
CLNSRC
CLNACC RCV000190219.1,