rs376106351
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs376106351(C;T) |
Make rs376106351(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 37506205 |
Gene | DYRK1A |
is a | snp |
is | mentioned by |
dbSNP | rs376106351 |
dbSNP (classic) | rs376106351 |
ClinGen | rs376106351 |
ebi | rs376106351 |
HLI | rs376106351 |
Exac | rs376106351 |
Gnomad | rs376106351 |
Varsome | rs376106351 |
LitVar | rs376106351 |
Map | rs376106351 |
PheGenI | rs376106351 |
Biobank | rs376106351 |
1000 genomes | rs376106351 |
hgdp | rs376106351 |
ensembl | rs376106351 |
geneview | rs376106351 |
scholar | rs376106351 |
rs376106351 | |
pharmgkb | rs376106351 |
gwascentral | rs376106351 |
openSNP | rs376106351 |
23andMe | rs376106351 |
SNPshot | rs376106351 |
SNPdbe | rs376106351 |
MSV3d | rs376106351 |
GWAS Ctlg | rs376106351 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376106351(A;A) rs376106351(T;T) |
Alt | rs376106351(A;A) rs376106351(T;T) |
Reference | Rs376106351(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYRK1A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.38878508C>A |
CLNSRC | |
CLNACC | RCV000481279.1, |