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rs281865066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865066(C;T)
Make rs281865066(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position63350533
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs281865066
ebirs281865066
HLIrs281865066
Exacrs281865066
Varsomers281865066
Maprs281865066
PheGenIrs281865066
hapmaprs281865066
1000 genomesrs281865066
hgdprs281865066
ensemblrs281865066
gopubmedrs281865066
geneviewrs281865066
scholarrs281865066
googlers281865066
pharmgkbrs281865066
gwascentralrs281865066
openSNPrs281865066
23andMers281865066
23andMe allrs281865066
SNP Nexus

SNPshotrs281865066
SNPdbers281865066
MSV3drs281865066
GWAS Ctlgrs281865066
Max Magnitude0
ClinVar
Risk rs281865066(T;T)
Alt rs281865066(T;T)
Reference rs281865066(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene CHRNA4
CLNDBN Epilepsy, nocturnal frontal lobe, type 1
Reversed 1
HGVS NC_000020.10:g.61981885G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000033928.2,