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rs281865072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281865072(G;G)
Make rs281865072(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position154571833
GeneCHRNB2
is asnp
is mentioned by
dbSNPrs281865072
ebirs281865072
HLIrs281865072
Exacrs281865072
Varsomers281865072
Maprs281865072
PheGenIrs281865072
hapmaprs281865072
1000 genomesrs281865072
hgdprs281865072
ensemblrs281865072
gopubmedrs281865072
geneviewrs281865072
scholarrs281865072
googlers281865072
pharmgkbrs281865072
gwascentralrs281865072
openSNPrs281865072
23andMers281865072
23andMe allrs281865072
SNP Nexus

SNPshotrs281865072
SNPdbers281865072
MSV3drs281865072
GWAS Ctlgrs281865072
Max Magnitude0
ClinVar
Risk rs281865072(A,G;A,G)
Alt rs281865072(A,G;A,G)
Reference rs281865072(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene CHRNB2
CLNDBN Epilepsy, nocturnal frontal lobe, type 3
Reversed 0
HGVS NC_000001.10:g.154544309T>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000033929.2,