rs2153271
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2153271(A;A) |
Make rs2153271(A;G) |
Make rs2153271(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 16864523 |
Gene | BNC2 |
is a | snp |
is | mentioned by |
dbSNP | rs2153271 |
dbSNP (classic) | rs2153271 |
ClinGen | rs2153271 |
ebi | rs2153271 |
HLI | rs2153271 |
Exac | rs2153271 |
Gnomad | rs2153271 |
Varsome | rs2153271 |
LitVar | rs2153271 |
Map | rs2153271 |
PheGenI | rs2153271 |
Biobank | rs2153271 |
1000 genomes | rs2153271 |
hgdp | rs2153271 |
ensembl | rs2153271 |
geneview | rs2153271 |
scholar | rs2153271 |
rs2153271 | |
pharmgkb | rs2153271 |
gwascentral | rs2153271 |
openSNP | rs2153271 |
23andMe | rs2153271 |
SNPshot | rs2153271 |
SNPdbe | rs2153271 |
MSV3d | rs2153271 |
GWAS Ctlg | rs2153271 |
GMAF | 0.3595 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
An association between freckling and rs2153271 10.1371/journal.pgen.1000993
GWAS snp | |
---|---|
PMID | [PMID 20585627] |
Trait | Freckling |
Title | Web-based, participant-driven studies yield novel genetic associations for common traits |
Risk Allele | C |
P-val | 4E-10 |
Odds Ratio | 0.40 [NR] unit decrease |