rs786205208
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs786205208(C;T) |
Make rs786205208(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | X |
Position | 74742675 |
Gene | KIAA2022 |
is a | snp |
is | mentioned by |
dbSNP | rs786205208 |
dbSNP (classic) | rs786205208 |
ClinGen | rs786205208 |
ebi | rs786205208 |
HLI | rs786205208 |
Exac | rs786205208 |
Gnomad | rs786205208 |
Varsome | rs786205208 |
LitVar | rs786205208 |
Map | rs786205208 |
PheGenI | rs786205208 |
Biobank | rs786205208 |
1000 genomes | rs786205208 |
hgdp | rs786205208 |
ensembl | rs786205208 |
geneview | rs786205208 |
scholar | rs786205208 |
rs786205208 | |
pharmgkb | rs786205208 |
gwascentral | rs786205208 |
openSNP | rs786205208 |
23andMe | rs786205208 |
SNPshot | rs786205208 |
SNPdbe | rs786205208 |
MSV3d | rs786205208 |
GWAS Ctlg | rs786205208 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205208(T;T) |
Alt | rs786205208(T;T) |
Reference | Rs786205208(C;C) |
Significance | Probable-Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | KIAA2022 |
CLNDBN | Mental retardation, X-linked 98 |
Reversed | 1 |
HGVS | NC_000023.10:g.73962510G>A |
CLNSRC | |
CLNACC | RCV000170439.1, |