rs2054847
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2054847(C;C) |
Make rs2054847(C;T) |
Make rs2054847(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 30204995 |
Gene | SLC6A4 |
is a | snp |
is | mentioned by |
dbSNP | rs2054847 |
dbSNP (classic) | rs2054847 |
ClinGen | rs2054847 |
ebi | rs2054847 |
HLI | rs2054847 |
Exac | rs2054847 |
Gnomad | rs2054847 |
Varsome | rs2054847 |
LitVar | rs2054847 |
Map | rs2054847 |
PheGenI | rs2054847 |
Biobank | rs2054847 |
1000 genomes | rs2054847 |
hgdp | rs2054847 |
ensembl | rs2054847 |
geneview | rs2054847 |
scholar | rs2054847 |
rs2054847 | |
pharmgkb | rs2054847 |
gwascentral | rs2054847 |
openSNP | rs2054847 |
23andMe | rs2054847 |
SNPshot | rs2054847 |
SNPdbe | rs2054847 |
MSV3d | rs2054847 |
GWAS Ctlg | rs2054847 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26408209] Common variants of HTR1A and SLC6A4 confer the increasing risk of Schizophrenia susceptibility: A population-based association and epistasis analysis