rs1105434
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1105434(A;A) |
Make rs1105434(A;G) |
Make rs1105434(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 56927585 |
Gene | REST |
is a | snp |
is | mentioned by |
dbSNP | rs1105434 |
dbSNP (classic) | rs1105434 |
ClinGen | rs1105434 |
ebi | rs1105434 |
HLI | rs1105434 |
Exac | rs1105434 |
Gnomad | rs1105434 |
Varsome | rs1105434 |
LitVar | rs1105434 |
Map | rs1105434 |
PheGenI | rs1105434 |
Biobank | rs1105434 |
1000 genomes | rs1105434 |
hgdp | rs1105434 |
ensembl | rs1105434 |
geneview | rs1105434 |
scholar | rs1105434 |
rs1105434 | |
pharmgkb | rs1105434 |
gwascentral | rs1105434 |
openSNP | rs1105434 |
23andMe | rs1105434 |
SNPshot | rs1105434 |
SNPdbe | rs1105434 |
MSV3d | rs1105434 |
GWAS Ctlg | rs1105434 |
GMAF | 0.3122 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18781183] An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4.