rs199422235
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199422235(C;C) |
Make rs199422235(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 53211867 |
Gene | KDM5C |
is a | snp |
is | mentioned by |
dbSNP | rs199422235 |
dbSNP (classic) | rs199422235 |
ClinGen | rs199422235 |
ebi | rs199422235 |
HLI | rs199422235 |
Exac | rs199422235 |
Gnomad | rs199422235 |
Varsome | rs199422235 |
LitVar | rs199422235 |
Map | rs199422235 |
PheGenI | rs199422235 |
Biobank | rs199422235 |
1000 genomes | rs199422235 |
hgdp | rs199422235 |
ensembl | rs199422235 |
geneview | rs199422235 |
scholar | rs199422235 |
rs199422235 | |
pharmgkb | rs199422235 |
gwascentral | rs199422235 |
openSNP | rs199422235 |
23andMe | rs199422235 |
SNPshot | rs199422235 |
SNPdbe | rs199422235 |
MSV3d | rs199422235 |
GWAS Ctlg | rs199422235 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199422235(C;C) |
Alt | rs199422235(C;C) |
Reference | Rs199422235(G;G) |
Significance | Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | KDM5C |
CLNDBN | Mental retardation, syndromic, Claes-Jensen type, X-linked |
Reversed | 1 |
HGVS | NC_000023.10:g.53241049C>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000010428.4, |