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rs193922637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922637(A;A)
Make rs193922637(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position113356784
GeneANK2
is asnp
is mentioned by
dbSNPrs193922637
dbSNP (classic)rs193922637
ClinGenrs193922637
ebirs193922637
HLIrs193922637
Exacrs193922637
Gnomadrs193922637
Varsomers193922637
LitVarrs193922637
Maprs193922637
PheGenIrs193922637
Biobankrs193922637
1000 genomesrs193922637
hgdprs193922637
ensemblrs193922637
geneviewrs193922637
scholarrs193922637
googlers193922637
pharmgkbrs193922637
gwascentralrs193922637
openSNPrs193922637
23andMers193922637
SNPshotrs193922637
SNPdbers193922637
MSV3drs193922637
GWAS Ctlgrs193922637
Max Magnitude0
ClinVar
Risk rs193922637(A;A)
Alt rs193922637(A;A)
Reference Rs193922637(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene ANK2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000004.11:g.114277940G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029339.1,