rs966321
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs966321(A;A) |
Make rs966321(A;C) |
Make rs966321(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 4255144 |
is a | snp |
is | mentioned by |
dbSNP | rs966321 |
dbSNP (classic) | rs966321 |
ClinGen | rs966321 |
ebi | rs966321 |
HLI | rs966321 |
Exac | rs966321 |
Gnomad | rs966321 |
Varsome | rs966321 |
LitVar | rs966321 |
Map | rs966321 |
PheGenI | rs966321 |
Biobank | rs966321 |
1000 genomes | rs966321 |
hgdp | rs966321 |
ensembl | rs966321 |
geneview | rs966321 |
scholar | rs966321 |
rs966321 | |
pharmgkb | rs966321 |
gwascentral | rs966321 |
openSNP | rs966321 |
23andMe | rs966321 |
SNPshot | rs966321 |
SNPdbe | rs966321 |
MSV3d | rs966321 |
GWAS Ctlg | rs966321 |
GMAF | 0.4022 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs966321 |
PubMedID | [PMID 17903294] |
Condition | Factor VII |
Gene | Intergenic |
Risk Allele | |
pValue | 8.00E-006 |
OR | NA |
95% CI |
[PMID 19340012] Genome-wide association study of tanning phenotype in a population of European ancestry.