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rs199794307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199794307(A;A)
Make rs199794307(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position5045060
GeneKCNA5
is asnp
is mentioned by
dbSNPrs199794307
ClinGenrs199794307
ebirs199794307
HLIrs199794307
Exacrs199794307
Varsomers199794307
Maprs199794307
PheGenIrs199794307
hapmaprs199794307
1000 genomesrs199794307
hgdprs199794307
ensemblrs199794307
gopubmedrs199794307
geneviewrs199794307
scholarrs199794307
googlers199794307
pharmgkbrs199794307
gwascentralrs199794307
openSNPrs199794307
23andMers199794307
23andMe allrs199794307
SNP Nexus

SNPshotrs199794307
SNPdbers199794307
MSV3drs199794307
GWAS Ctlgrs199794307
Max Magnitude0
ClinVar
Risk rs199794307(A;A)
Alt rs199794307(A;A)
Reference Rs199794307(G;G)
Significance Pathogenic
Disease Atrial fibrillation not provided
Variation info
Gene KCNA5
CLNDBN Atrial fibrillation, familial, 7 not provided
Reversed 0
HGVS NC_000012.11:g.5154226G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114990.3, RCV000171655.1,