rs17339677
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs17339677(A;A) |
Make rs17339677(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 3072433 |
Gene | LOC101929098, OXT |
is a | snp |
is | mentioned by |
dbSNP | rs17339677 |
dbSNP (classic) | rs17339677 |
ClinGen | rs17339677 |
ebi | rs17339677 |
HLI | rs17339677 |
Exac | rs17339677 |
Gnomad | rs17339677 |
Varsome | rs17339677 |
LitVar | rs17339677 |
Map | rs17339677 |
PheGenI | rs17339677 |
Biobank | rs17339677 |
1000 genomes | rs17339677 |
hgdp | rs17339677 |
ensembl | rs17339677 |
geneview | rs17339677 |
scholar | rs17339677 |
rs17339677 | |
pharmgkb | rs17339677 |
gwascentral | rs17339677 |
openSNP | rs17339677 |
23andMe | rs17339677 |
SNPshot | rs17339677 |
SNPdbe | rs17339677 |
MSV3d | rs17339677 |
GWAS Ctlg | rs17339677 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19473710] Mutation analysis of oxytocin gene in individuals with adult separation anxiety
[PMID 18566739] Variation of the oxytocin/neurophysin I (OXT) gene in four human populations.