rs17159614
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs17159614(C;T) |
Make rs17159614(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 85096186 |
Gene | SEMA3D |
is a | snp |
is | mentioned by |
dbSNP | rs17159614 |
dbSNP (classic) | rs17159614 |
ClinGen | rs17159614 |
ebi | rs17159614 |
HLI | rs17159614 |
Exac | rs17159614 |
Gnomad | rs17159614 |
Varsome | rs17159614 |
LitVar | rs17159614 |
Map | rs17159614 |
PheGenI | rs17159614 |
Biobank | rs17159614 |
1000 genomes | rs17159614 |
hgdp | rs17159614 |
ensembl | rs17159614 |
geneview | rs17159614 |
scholar | rs17159614 |
rs17159614 | |
pharmgkb | rs17159614 |
gwascentral | rs17159614 |
openSNP | rs17159614 |
23andMe | rs17159614 |
SNPshot | rs17159614 |
SNPdbe | rs17159614 |
MSV3d | rs17159614 |
GWAS Ctlg | rs17159614 |
GMAF | 0.07484 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20684831] Possible association of the semaphorin 3D gene (SEMA3D) with schizophrenia