rs989638
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs989638(A;A) |
Make rs989638(A;G) |
Make rs989638(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 123239256 |
Gene | GRIA3 |
is a | snp |
is | mentioned by |
dbSNP | rs989638 |
dbSNP (classic) | rs989638 |
ClinGen | rs989638 |
ebi | rs989638 |
HLI | rs989638 |
Exac | rs989638 |
Gnomad | rs989638 |
Varsome | rs989638 |
LitVar | rs989638 |
Map | rs989638 |
PheGenI | rs989638 |
Biobank | rs989638 |
1000 genomes | rs989638 |
hgdp | rs989638 |
ensembl | rs989638 |
geneview | rs989638 |
scholar | rs989638 |
rs989638 | |
pharmgkb | rs989638 |
gwascentral | rs989638 |
openSNP | rs989638 |
23andMe | rs989638 |
SNPshot | rs989638 |
SNPdbe | rs989638 |
MSV3d | rs989638 |
GWAS Ctlg | rs989638 |
GMAF | 0.1892 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
This SNP is part of a specific haplotype, rs989638-rs1034428-rs2227098 G-T-G (as oriented with respect to dbSNP) with an overall ~2x higher risk in females for schizophrenia (p=0.0008). [PMID 18163426]