rs183211
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs183211(A;A) |
Make rs183211(A;G) |
Make rs183211(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 46710944 |
Gene | NSF |
is a | snp |
is | mentioned by |
dbSNP | rs183211 |
dbSNP (classic) | rs183211 |
ClinGen | rs183211 |
ebi | rs183211 |
HLI | rs183211 |
Exac | rs183211 |
Gnomad | rs183211 |
Varsome | rs183211 |
LitVar | rs183211 |
Map | rs183211 |
PheGenI | rs183211 |
Biobank | rs183211 |
1000 genomes | rs183211 |
hgdp | rs183211 |
ensembl | rs183211 |
geneview | rs183211 |
scholar | rs183211 |
rs183211 | |
pharmgkb | rs183211 |
gwascentral | rs183211 |
openSNP | rs183211 |
23andMe | rs183211 |
SNPshot | rs183211 |
SNPdbe | rs183211 |
MSV3d | rs183211 |
GWAS Ctlg | rs183211 |
GMAF | 0.4146 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21812969] |
Trait | |
Title | Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. |
Risk Allele | T |
P-val | 3E-7 |
Odds Ratio | None None |
GWAS snp | |
---|---|
PMID | [PMID 23544013] |
Trait | Ovarian cancer in BRCA1 mutation carriers |
Title | Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. |
Risk Allele | A |
P-val | 3E-8 |
Odds Ratio | 1.25 [1.16-1.35] |