rs879253771
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;CA) | 3 | speech and other processing issues possible |
(AC;AC) | 0 | common in clinvar |
Make rs879253771(-;-) |
Make rs879253771(CA;CA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 114652276 |
Gene | FOXP2, MIR3666 |
is a | snp |
is | mentioned by |
dbSNP | rs879253771 |
dbSNP (classic) | rs879253771 |
ClinGen | rs879253771 |
ebi | rs879253771 |
HLI | rs879253771 |
Exac | rs879253771 |
Gnomad | rs879253771 |
Varsome | rs879253771 |
LitVar | rs879253771 |
Map | rs879253771 |
PheGenI | rs879253771 |
Biobank | rs879253771 |
1000 genomes | rs879253771 |
hgdp | rs879253771 |
ensembl | rs879253771 |
geneview | rs879253771 |
scholar | rs879253771 |
rs879253771 | |
pharmgkb | rs879253771 |
gwascentral | rs879253771 |
openSNP | rs879253771 |
23andMe | rs879253771 |
SNPshot | rs879253771 |
SNPdbe | rs879253771 |
MSV3d | rs879253771 |
GWAS Ctlg | rs879253771 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs879253771(-;-) |
Alt | rs879253771(-;-) |
Reference | Rs879253771(AC;AC) |
Significance | Pathogenic |
Disease | Speech-language disorder 1 |
Variation | info |
Gene | FOXP2 MIR3666 |
CLNDBN | Speech-language disorder 1 |
Reversed | 0 |
HGVS | NC_000007.13:g.114292331_114292332delCA |
CLNSRC | |
CLNACC | RCV000234941.1, |