rs12410279
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12410279(A;A) |
Make rs12410279(A;G) |
Make rs12410279(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 220678178 |
is a | snp |
is | mentioned by |
dbSNP | rs12410279 |
dbSNP (classic) | rs12410279 |
ClinGen | rs12410279 |
ebi | rs12410279 |
HLI | rs12410279 |
Exac | rs12410279 |
Gnomad | rs12410279 |
Varsome | rs12410279 |
LitVar | rs12410279 |
Map | rs12410279 |
PheGenI | rs12410279 |
Biobank | rs12410279 |
1000 genomes | rs12410279 |
hgdp | rs12410279 |
ensembl | rs12410279 |
geneview | rs12410279 |
scholar | rs12410279 |
rs12410279 | |
pharmgkb | rs12410279 |
gwascentral | rs12410279 |
openSNP | rs12410279 |
23andMe | rs12410279 |
SNPshot | rs12410279 |
SNPdbe | rs12410279 |
MSV3d | rs12410279 |
GWAS Ctlg | rs12410279 |
GMAF | 0.2112 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18492799] Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a relative risk for autism of 1.8 in homozygous carriers