Rs121909580

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909580(C;T)
Make rs121909580(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position63350572
GeneCHRNA4
is asnp
is mentioned by
dbSNPrs121909580
Exacrs121909580
PheGenIrs121909580
nextbiors121909580
hapmaprs121909580
1000 genomesrs121909580
hgdprs121909580
ensemblrs121909580
gopubmedrs121909580
geneviewrs121909580
scholarrs121909580
googlers121909580
pharmgkbrs121909580
gwascentralrs121909580
openSNPrs121909580
23andMers121909580
23andMe allrs121909580
SNP Nexus

SNPshotrs121909580
SNPdbers121909580
MSV3drs121909580
OMIM118504
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909580(T;T)
Alt rs121909580(T;T)
Reference rs121909580(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene CHRNA4
CLNDBN Epilepsy, nocturnal frontal lobe, type 1
Reversed 1
HGVS NC_000020.10:g.61981924G>A
CLNSRC GeneReviews OMIM Allelic Variant
CLNACC RCV000019050.23,