rs12931267
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs12931267(C;G) |
Make rs12931267(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 89752324 |
Gene | FANCA |
is a | snp |
is | mentioned by |
dbSNP | rs12931267 |
dbSNP (classic) | rs12931267 |
ClinGen | rs12931267 |
ebi | rs12931267 |
HLI | rs12931267 |
Exac | rs12931267 |
Gnomad | rs12931267 |
Varsome | rs12931267 |
LitVar | rs12931267 |
Map | rs12931267 |
PheGenI | rs12931267 |
Biobank | rs12931267 |
1000 genomes | rs12931267 |
hgdp | rs12931267 |
ensembl | rs12931267 |
geneview | rs12931267 |
scholar | rs12931267 |
rs12931267 | |
pharmgkb | rs12931267 |
gwascentral | rs12931267 |
openSNP | rs12931267 |
23andMe | rs12931267 |
SNPshot | rs12931267 |
SNPdbe | rs12931267 |
MSV3d | rs12931267 |
GWAS Ctlg | rs12931267 |
GMAF | 0.03627 |
Max Magnitude | 0 |
10.1371/journal.pgen.1000993 hair color
GWAS snp | |
---|---|
PMID | [PMID 20585627] |
Trait | Freckling |
Title | Web-based, participant-driven studies yield novel genetic associations for common traits |
Risk Allele | G |
P-val | 8E-62 |
Odds Ratio | 1.88 [NR] unit increase |