rs144902457
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs144902457(C;C) |
Make rs144902457(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 123253500 |
Gene | GRIA3 |
is a | snp |
is | mentioned by |
dbSNP | rs144902457 |
dbSNP (classic) | rs144902457 |
ClinGen | rs144902457 |
ebi | rs144902457 |
HLI | rs144902457 |
Exac | rs144902457 |
Gnomad | rs144902457 |
Varsome | rs144902457 |
LitVar | rs144902457 |
Map | rs144902457 |
PheGenI | rs144902457 |
Biobank | rs144902457 |
1000 genomes | rs144902457 |
hgdp | rs144902457 |
ensembl | rs144902457 |
geneview | rs144902457 |
scholar | rs144902457 |
rs144902457 | |
pharmgkb | rs144902457 |
gwascentral | rs144902457 |
openSNP | rs144902457 |
23andMe | rs144902457 |
SNPshot | rs144902457 |
SNPdbe | rs144902457 |
MSV3d | rs144902457 |
GWAS Ctlg | rs144902457 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs144902457(C;C) |
Alt | rs144902457(C;C) |
Reference | Rs144902457(T;T) |
Significance | Probable-non-pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | GRIA3 |
CLNDBN | Mental retardation, X-linked, syndromic, wu type |
Reversed | 0 |
HGVS | NC_000023.10:g.122387351T>C |
CLNSRC | |
CLNACC | RCV000209928.2, |