rs780441716
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs780441716(C;T) |
Make rs780441716(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 37490201 |
Gene | DYRK1A, LOC105372797 |
is a | snp |
is | mentioned by |
dbSNP | rs780441716 |
dbSNP (classic) | rs780441716 |
ClinGen | rs780441716 |
ebi | rs780441716 |
HLI | rs780441716 |
Exac | rs780441716 |
Gnomad | rs780441716 |
Varsome | rs780441716 |
LitVar | rs780441716 |
Map | rs780441716 |
PheGenI | rs780441716 |
Biobank | rs780441716 |
1000 genomes | rs780441716 |
hgdp | rs780441716 |
ensembl | rs780441716 |
geneview | rs780441716 |
scholar | rs780441716 |
rs780441716 | |
pharmgkb | rs780441716 |
gwascentral | rs780441716 |
openSNP | rs780441716 |
23andMe | rs780441716 |
SNPshot | rs780441716 |
SNPdbe | rs780441716 |
MSV3d | rs780441716 |
GWAS Ctlg | rs780441716 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs780441716(T;T) |
Alt | rs780441716(T;T) |
Reference | Rs780441716(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYRK1A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.38862503C>T |
CLNSRC | |
CLNACC | RCV000481862.1, |