rs398124506
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GC;GC) | 0 | common in clinvar |
Make rs398124506(-;-) |
Make rs398124506(-;GC) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 25007407 |
Gene | ARX |
is a | snp |
is | mentioned by |
dbSNP | rs398124506 |
dbSNP (classic) | rs398124506 |
ClinGen | rs398124506 |
ebi | rs398124506 |
HLI | rs398124506 |
Exac | rs398124506 |
Gnomad | rs398124506 |
Varsome | rs398124506 |
LitVar | rs398124506 |
Map | rs398124506 |
PheGenI | rs398124506 |
Biobank | rs398124506 |
1000 genomes | rs398124506 |
hgdp | rs398124506 |
ensembl | rs398124506 |
geneview | rs398124506 |
scholar | rs398124506 |
rs398124506 | |
pharmgkb | rs398124506 |
gwascentral | rs398124506 |
openSNP | rs398124506 |
23andMe | rs398124506 |
SNPshot | rs398124506 |
SNPdbe | rs398124506 |
MSV3d | rs398124506 |
GWAS Ctlg | rs398124506 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398124506(-;-) |
Alt | rs398124506(-;-) |
Reference | Rs398124506(GC;GC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ARX |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.25025524_25025525delGC |
CLNSRC | ClinVar |
CLNACC | RCV000082598.4, |