rs7142002
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs7142002(C;C) |
Make rs7142002(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 101894408 |
Gene | PPP2R5C |
is a | snp |
is | mentioned by |
dbSNP | rs7142002 |
dbSNP (classic) | rs7142002 |
ClinGen | rs7142002 |
ebi | rs7142002 |
HLI | rs7142002 |
Exac | rs7142002 |
Gnomad | rs7142002 |
Varsome | rs7142002 |
LitVar | rs7142002 |
Map | rs7142002 |
PheGenI | rs7142002 |
Biobank | rs7142002 |
1000 genomes | rs7142002 |
hgdp | rs7142002 |
ensembl | rs7142002 |
geneview | rs7142002 |
scholar | rs7142002 |
rs7142002 | |
pharmgkb | rs7142002 |
gwascentral | rs7142002 |
openSNP | rs7142002 |
23andMe | rs7142002 |
SNPshot | rs7142002 |
SNPdbe | rs7142002 |
MSV3d | rs7142002 |
GWAS Ctlg | rs7142002 |
GMAF | 0.1152 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20663923] |
Trait | Autism |
Title | A genomewide scan for common alleles affecting risk for autism |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | 1.56 [1.28-1.89] |