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rs281865070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281865070(C;C)
Make rs281865070(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position154571746
GeneCHRNB2
is asnp
is mentioned by
dbSNPrs281865070
ebirs281865070
HLIrs281865070
Exacrs281865070
Varsomers281865070
Maprs281865070
PheGenIrs281865070
hapmaprs281865070
1000 genomesrs281865070
hgdprs281865070
ensemblrs281865070
gopubmedrs281865070
geneviewrs281865070
scholarrs281865070
googlers281865070
pharmgkbrs281865070
gwascentralrs281865070
openSNPrs281865070
23andMers281865070
23andMe allrs281865070
SNP Nexus

SNPshotrs281865070
SNPdbers281865070
MSV3drs281865070
GWAS Ctlgrs281865070
Max Magnitude0
ClinVar
Risk rs281865070(C;C)
Alt rs281865070(C;C)
Reference rs281865070(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene CHRNB2
CLNDBN Epilepsy, nocturnal frontal lobe, type 3
Reversed 0
HGVS NC_000001.10:g.154544222T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000033932.2,