rs6537825
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6537825(A;A) |
Make rs6537825(A;G) |
Make rs6537825(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 114405659 |
Gene | TRIM33 |
is a | snp |
is | mentioned by |
dbSNP | rs6537825 |
dbSNP (classic) | rs6537825 |
ClinGen | rs6537825 |
ebi | rs6537825 |
HLI | rs6537825 |
Exac | rs6537825 |
Gnomad | rs6537825 |
Varsome | rs6537825 |
LitVar | rs6537825 |
Map | rs6537825 |
PheGenI | rs6537825 |
Biobank | rs6537825 |
1000 genomes | rs6537825 |
hgdp | rs6537825 |
ensembl | rs6537825 |
geneview | rs6537825 |
scholar | rs6537825 |
rs6537825 | |
pharmgkb | rs6537825 |
gwascentral | rs6537825 |
openSNP | rs6537825 |
23andMe | rs6537825 |
SNPshot | rs6537825 |
SNPdbe | rs6537825 |
MSV3d | rs6537825 |
GWAS Ctlg | rs6537825 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24189344] |
Trait | Autism |
Title | Common genetic variants on 1p13.2 associate with risk of autism. |
Risk Allele | A |
P-val | 3E-8 |
Odds Ratio | 1.40 [NR] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d