rs1015657
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1015657(C;C) |
Make rs1015657(C;T) |
Make rs1015657(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 70882346 |
is a | snp |
is | mentioned by |
dbSNP | rs1015657 |
dbSNP (classic) | rs1015657 |
ClinGen | rs1015657 |
ebi | rs1015657 |
HLI | rs1015657 |
Exac | rs1015657 |
Gnomad | rs1015657 |
Varsome | rs1015657 |
LitVar | rs1015657 |
Map | rs1015657 |
PheGenI | rs1015657 |
Biobank | rs1015657 |
1000 genomes | rs1015657 |
hgdp | rs1015657 |
ensembl | rs1015657 |
geneview | rs1015657 |
scholar | rs1015657 |
rs1015657 | |
pharmgkb | rs1015657 |
gwascentral | rs1015657 |
openSNP | rs1015657 |
23andMe | rs1015657 |
SNPshot | rs1015657 |
SNPdbe | rs1015657 |
MSV3d | rs1015657 |
GWAS Ctlg | rs1015657 |
GMAF | 0.3659 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22648509] |
Trait | |
Title | PKNOX2 is Associated with Formal Thought Disorder in Schizophrenia: a Meta-Analysis of Two Genome-wide Association Studies. |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | 1.3200 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 17
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d