Rs121909580

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Orientationminus
is asnp
is mentioned by
dbSNPrs121909580
PheGenIrs121909580
nextbiors121909580
hapmaprs121909580
1000 genomesrs121909580
hgdprs121909580
ensemblrs121909580
gopubmedrs121909580
geneviewrs121909580
scholarrs121909580
googlers121909580
pharmgkbrs121909580
gwascentralrs121909580
openSNPrs121909580
23andMers121909580
23andMe allrs121909580
SNP Nexus

SNPshotrs121909580
SNPdbers121909580
MSV3drs121909580
GeneCHRNA4
Chromosome20
Orientationminus
Position61981924
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909580(C;T)
Make rs121909580(T;T)
OMIM118504
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909580(T;T)
Alt rs121909580(T;T)
Reference rs121909580(C;C)
Significance 5
Disease Epilepsy
ClinVar info
Gene CHRNA4
CLNDBN Epilepsy, nocturnal frontal lobe, type 1
Reversed 1
CLNHGVS NC_000020.10:g.61981924G>A
CLNSRC GeneReviews, OMIM Allelic Variant
CLNACC RCV000019050.23