rs56142442
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs56142442(C;T) |
Make rs56142442(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 85021350 |
Gene | NTRK2 |
is a | snp |
is | mentioned by |
dbSNP | rs56142442 |
dbSNP (classic) | rs56142442 |
ClinGen | rs56142442 |
ebi | rs56142442 |
HLI | rs56142442 |
Exac | rs56142442 |
Gnomad | rs56142442 |
Varsome | rs56142442 |
LitVar | rs56142442 |
Map | rs56142442 |
PheGenI | rs56142442 |
Biobank | rs56142442 |
1000 genomes | rs56142442 |
hgdp | rs56142442 |
ensembl | rs56142442 |
geneview | rs56142442 |
scholar | rs56142442 |
rs56142442 | |
pharmgkb | rs56142442 |
gwascentral | rs56142442 |
openSNP | rs56142442 |
23andMe | rs56142442 |
SNPshot | rs56142442 |
SNPdbe | rs56142442 |
MSV3d | rs56142442 |
GWAS Ctlg | rs56142442 |
GMAF | 0.00551 |
Max Magnitude | 0 |
[PMID 19844206] Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans
ClinVar | |
---|---|
Risk | rs56142442(T;T) |
Alt | rs56142442(T;T) |
Reference | Rs56142442(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | NTRK2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000009.11:g.87636265C>T |
CLNSRC | |
CLNACC | RCV000273344.1, |
[PMID 30308049] The TRKB rs2289656 genetic polymorphism is associated with acute suicide attempts in depressed patients: A transversal case control study.