rs387906703
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs387906703(A;T) |
Make rs387906703(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 20195128 |
Gene | RPS6KA3 |
is a | snp |
is | mentioned by |
dbSNP | rs387906703 |
dbSNP (classic) | rs387906703 |
ClinGen | rs387906703 |
ebi | rs387906703 |
HLI | rs387906703 |
Exac | rs387906703 |
Gnomad | rs387906703 |
Varsome | rs387906703 |
LitVar | rs387906703 |
Map | rs387906703 |
PheGenI | rs387906703 |
Biobank | rs387906703 |
1000 genomes | rs387906703 |
hgdp | rs387906703 |
ensembl | rs387906703 |
geneview | rs387906703 |
scholar | rs387906703 |
rs387906703 | |
pharmgkb | rs387906703 |
gwascentral | rs387906703 |
openSNP | rs387906703 |
23andMe | rs387906703 |
SNPshot | rs387906703 |
SNPdbe | rs387906703 |
MSV3d | rs387906703 |
GWAS Ctlg | rs387906703 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906703(T;T) |
Alt | rs387906703(T;T) |
Reference | Rs387906703(A;A) |
Significance | Pathogenic |
Disease | Mental retardation |
Variation | info |
Gene | RPS6KA3 |
CLNDBN | Mental retardation, X-linked 19 |
Reversed | 1 |
HGVS | NC_000023.10:g.20213246T>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000022823.27, |