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rs281865067

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs281865067(-;-)
Make rs281865067(-;GCT)
Make rs281865067(GCT;GCT)
ReferenceGRCh38 38.1/141
Chromosome20
Position63350538
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs281865067
ebirs281865067
HLIrs281865067
Exacrs281865067
Varsomers281865067
Maprs281865067
PheGenIrs281865067
hapmaprs281865067
1000 genomesrs281865067
hgdprs281865067
ensemblrs281865067
gopubmedrs281865067
geneviewrs281865067
scholarrs281865067
googlers281865067
pharmgkbrs281865067
gwascentralrs281865067
openSNPrs281865067
23andMers281865067
23andMe allrs281865067
SNP Nexus

SNPshotrs281865067
SNPdbers281865067
MSV3drs281865067
GWAS Ctlgrs281865067
Max Magnitude0
ClinVar
Risk rs281865067(GCT;GCT)
Alt rs281865067(GCT;GCT)
Reference rs281865067(;)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene CHRNA4
CLNDBN Epilepsy, nocturnal frontal lobe, type 1
Reversed 1
HGVS NC_000020.10:g.61981891_61981893dupAGC
CLNSRC ClinVar GeneReviews
CLNACC RCV000033927.2,