rs2020934
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2020934(C;C) |
Make rs2020934(C;T) |
Make rs2020934(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 30234442 |
Gene | SLC6A4 |
is a | snp |
is | mentioned by |
dbSNP | rs2020934 |
dbSNP (classic) | rs2020934 |
ClinGen | rs2020934 |
ebi | rs2020934 |
HLI | rs2020934 |
Exac | rs2020934 |
Gnomad | rs2020934 |
Varsome | rs2020934 |
LitVar | rs2020934 |
Map | rs2020934 |
PheGenI | rs2020934 |
Biobank | rs2020934 |
1000 genomes | rs2020934 |
hgdp | rs2020934 |
ensembl | rs2020934 |
geneview | rs2020934 |
scholar | rs2020934 |
rs2020934 | |
pharmgkb | rs2020934 |
gwascentral | rs2020934 |
openSNP | rs2020934 |
23andMe | rs2020934 |
SNPshot | rs2020934 |
SNPdbe | rs2020934 |
MSV3d | rs2020934 |
GWAS Ctlg | rs2020934 |
GMAF | 0.4995 |
Max Magnitude | 0 |
[PMID 15995945] Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.