rs2302763
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs2302763(C;C) |
Make rs2302763(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 7455958 |
Gene | CHRNB1 |
is a | snp |
is | mentioned by |
dbSNP | rs2302763 |
dbSNP (classic) | rs2302763 |
ClinGen | rs2302763 |
ebi | rs2302763 |
HLI | rs2302763 |
Exac | rs2302763 |
Gnomad | rs2302763 |
Varsome | rs2302763 |
LitVar | rs2302763 |
Map | rs2302763 |
PheGenI | rs2302763 |
Biobank | rs2302763 |
1000 genomes | rs2302763 |
hgdp | rs2302763 |
ensembl | rs2302763 |
geneview | rs2302763 |
scholar | rs2302763 |
rs2302763 | |
pharmgkb | rs2302763 |
gwascentral | rs2302763 |
openSNP | rs2302763 |
23andMe | rs2302763 |
SNPshot | rs2302763 |
SNPdbe | rs2302763 |
MSV3d | rs2302763 |
GWAS Ctlg | rs2302763 |
GMAF | 0.1717 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Variations in this snp have been linked to nicotine dependence [PMID 16874522]
[PMID 19259974] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.
ClinVar | |
---|---|
Risk | rs2302763(C;C) |
Alt | rs2302763(C;C) |
Reference | Rs2302763(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CHRNB1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000017.10:g.7359277T>C |
CLNSRC | |
CLNACC | RCV000242294.2, |