Have questions? Visit https://www.reddit.com/r/SNPedia

rs4845378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4845378(G;T)
Make rs4845378(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position154572175
GeneCHRNB2
is asnp
is mentioned by
dbSNPrs4845378
ebirs4845378
HLIrs4845378
Exacrs4845378
Varsomers4845378
Maprs4845378
PheGenIrs4845378
hapmaprs4845378
1000 genomesrs4845378
hgdprs4845378
ensemblrs4845378
gopubmedrs4845378
geneviewrs4845378
scholarrs4845378
googlers4845378
pharmgkbrs4845378
gwascentralrs4845378
openSNPrs4845378
23andMers4845378
23andMe allrs4845378
SNP Nexus

SNPshotrs4845378
SNPdbers4845378
MSV3drs4845378
GWAS Ctlgrs4845378
GMAF0.1061
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 19482438] Association of genes coding for the alpha-4, alpha-5, beta-2 and beta-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence

[PMID 18813964OA-icon.png] Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta.

[PMID 18830724OA-icon.png] Assessment of Alzheimer's disease case-control associations using family-based methods.

[PMID 20574532OA-icon.png] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.


ClinVar
Risk rs4845378(T;T)
Alt rs4845378(T;T)
Reference rs4845378(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene CHRNB2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.154544651G>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000145708.1,