rs797045584
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs797045584(C;T) |
Make rs797045584(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 70976964 |
Gene | FOXP1 |
is a | snp |
is | mentioned by |
dbSNP | rs797045584 |
dbSNP (classic) | rs797045584 |
ClinGen | rs797045584 |
ebi | rs797045584 |
HLI | rs797045584 |
Exac | rs797045584 |
Gnomad | rs797045584 |
Varsome | rs797045584 |
LitVar | rs797045584 |
Map | rs797045584 |
PheGenI | rs797045584 |
Biobank | rs797045584 |
1000 genomes | rs797045584 |
hgdp | rs797045584 |
ensembl | rs797045584 |
geneview | rs797045584 |
scholar | rs797045584 |
rs797045584 | |
pharmgkb | rs797045584 |
gwascentral | rs797045584 |
openSNP | rs797045584 |
23andMe | rs797045584 |
SNPshot | rs797045584 |
SNPdbe | rs797045584 |
MSV3d | rs797045584 |
GWAS Ctlg | rs797045584 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045584(T;T) |
Alt | rs797045584(T;T) |
Reference | Rs797045584(C;C) |
Significance | Pathogenic |
Disease | Mental retardation with language impairment and with or without autistic features not provided |
Variation | info |
Gene | FOXP1 |
CLNDBN | Mental retardation with language impairment and with or without autistic features not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.71026115G>A |
CLNSRC | |
CLNACC | RCV000195136.1, RCV000423150.1, |