rs878853141
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878853141(C;C) |
Make rs878853141(C;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 53199068 |
Gene | KDM5C, MIR6894 |
is a | snp |
is | mentioned by |
dbSNP | rs878853141 |
dbSNP (classic) | rs878853141 |
ClinGen | rs878853141 |
ebi | rs878853141 |
HLI | rs878853141 |
Exac | rs878853141 |
Gnomad | rs878853141 |
Varsome | rs878853141 |
LitVar | rs878853141 |
Map | rs878853141 |
PheGenI | rs878853141 |
Biobank | rs878853141 |
1000 genomes | rs878853141 |
hgdp | rs878853141 |
ensembl | rs878853141 |
geneview | rs878853141 |
scholar | rs878853141 |
rs878853141 | |
pharmgkb | rs878853141 |
gwascentral | rs878853141 |
openSNP | rs878853141 |
23andMe | rs878853141 |
SNPshot | rs878853141 |
SNPdbe | rs878853141 |
MSV3d | rs878853141 |
GWAS Ctlg | rs878853141 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853141(C;C) |
Alt | rs878853141(C;C) |
Reference | Rs878853141(G;G) |
Significance | Pathogenic |
Disease | Intellectual disability |
Variation | info |
Gene | KDM5C MIR6894 |
CLNDBN | Intellectual disability |
Reversed | 1 |
HGVS | NC_000023.10:g.53228250C>G |
CLNSRC | |
CLNACC | RCV000224884.1, |