rs2229944
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2229944(C;T) |
Make rs2229944(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 161294312 |
Gene | GABRB2 |
is a | snp |
is | mentioned by |
dbSNP | rs2229944 |
dbSNP (classic) | rs2229944 |
ClinGen | rs2229944 |
ebi | rs2229944 |
HLI | rs2229944 |
Exac | rs2229944 |
Gnomad | rs2229944 |
Varsome | rs2229944 |
LitVar | rs2229944 |
Map | rs2229944 |
PheGenI | rs2229944 |
Biobank | rs2229944 |
1000 genomes | rs2229944 |
hgdp | rs2229944 |
ensembl | rs2229944 |
geneview | rs2229944 |
scholar | rs2229944 |
rs2229944 | |
pharmgkb | rs2229944 |
gwascentral | rs2229944 |
openSNP | rs2229944 |
23andMe | rs2229944 |
SNPshot | rs2229944 |
SNPdbe | rs2229944 |
MSV3d | rs2229944 |
GWAS Ctlg | rs2229944 |
GMAF | 0.1088 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20404824] Imprinting in the schizophrenia candidate gene GABRB2 encoding GABA(A) receptor beta(2) subunit
ClinVar | |
---|---|
Risk | rs2229944(T;T) |
Alt | rs2229944(T;T) |
Reference | Rs2229944(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | GABRB2 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000005.9:g.160721319G>A |
CLNSRC | |
CLNACC | RCV000429656.1, |