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rs786205420

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205420(C;T)
Make rs786205420(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position113293537
GeneANK2
is asnp
is mentioned by
dbSNPrs786205420
dbSNP (classic)rs786205420
ClinGenrs786205420
ebirs786205420
HLIrs786205420
Exacrs786205420
Gnomadrs786205420
Varsomers786205420
LitVarrs786205420
Maprs786205420
PheGenIrs786205420
Biobankrs786205420
1000 genomesrs786205420
hgdprs786205420
ensemblrs786205420
geneviewrs786205420
scholarrs786205420
googlers786205420
pharmgkbrs786205420
gwascentralrs786205420
openSNPrs786205420
23andMers786205420
SNPshotrs786205420
SNPdbers786205420
MSV3drs786205420
GWAS Ctlgrs786205420
Max Magnitude0
ClinVar
Risk rs786205420(T;T)
Alt rs786205420(T;T)
Reference Rs786205420(C;C)
Significance Probable-Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene ANK2
CLNDBN not provided Long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114214693C>T
CLNSRC
CLNACC RCV000171593.1, RCV000190218.1,