rs189437004
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs189437004(A;A) |
Make rs189437004(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 123326097 |
Gene | GRIA3 |
is a | snp |
is | mentioned by |
dbSNP | rs189437004 |
dbSNP (classic) | rs189437004 |
ClinGen | rs189437004 |
ebi | rs189437004 |
HLI | rs189437004 |
Exac | rs189437004 |
Gnomad | rs189437004 |
Varsome | rs189437004 |
LitVar | rs189437004 |
Map | rs189437004 |
PheGenI | rs189437004 |
Biobank | rs189437004 |
1000 genomes | rs189437004 |
hgdp | rs189437004 |
ensembl | rs189437004 |
geneview | rs189437004 |
scholar | rs189437004 |
rs189437004 | |
pharmgkb | rs189437004 |
gwascentral | rs189437004 |
openSNP | rs189437004 |
23andMe | rs189437004 |
SNPshot | rs189437004 |
SNPdbe | rs189437004 |
MSV3d | rs189437004 |
GWAS Ctlg | rs189437004 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs189437004(A;A) |
Alt | rs189437004(A;A) |
Reference | Rs189437004(G;G) |
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.122459948G>A |
CLNSRC | |
CLNACC | RCV000209883.3, |