rs1861050
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs1861050(C;T) |
Make rs1861050(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 15480736 |
Gene | CC2D2A |
is a | snp |
is | mentioned by |
dbSNP | rs1861050 |
dbSNP (classic) | rs1861050 |
ClinGen | rs1861050 |
ebi | rs1861050 |
HLI | rs1861050 |
Exac | rs1861050 |
Gnomad | rs1861050 |
Varsome | rs1861050 |
LitVar | rs1861050 |
Map | rs1861050 |
PheGenI | rs1861050 |
Biobank | rs1861050 |
1000 genomes | rs1861050 |
hgdp | rs1861050 |
ensembl | rs1861050 |
geneview | rs1861050 |
scholar | rs1861050 |
rs1861050 | |
pharmgkb | rs1861050 |
gwascentral | rs1861050 |
openSNP | rs1861050 |
23andMe | rs1861050 |
SNPshot | rs1861050 |
SNPdbe | rs1861050 |
MSV3d | rs1861050 |
GWAS Ctlg | rs1861050 |
GMAF | 0.1107 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324] |
Trait | Conduct disorder (case status) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | 1.63 [1.31-2.01] |
ClinVar | |
---|---|
Risk | rs1861050(T;T) |
Alt | rs1861050(T;T) |
Reference | Rs1861050(C;C) |
Significance | Other |
Disease | not specified Joubert syndrome Meckel-Gruber syndrome |
Variation | info |
Gene | CC2D2A |
CLNDBN | not specified Joubert syndrome Meckel-Gruber syndrome |
Reversed | 0 |
HGVS | NC_000004.11:g.15482360C>T |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000114165.3, RCV000269461.1, RCV000329244.1, |