rs1039571136
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1039571136(C;T) |
Make rs1039571136(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 37490442 |
Gene | DYRK1A, LOC105372797 |
is a | snp |
is | mentioned by |
dbSNP | rs1039571136 |
dbSNP (classic) | rs1039571136 |
ClinGen | rs1039571136 |
ebi | rs1039571136 |
HLI | rs1039571136 |
Exac | rs1039571136 |
Gnomad | rs1039571136 |
Varsome | rs1039571136 |
LitVar | rs1039571136 |
Map | rs1039571136 |
PheGenI | rs1039571136 |
Biobank | rs1039571136 |
1000 genomes | rs1039571136 |
hgdp | rs1039571136 |
ensembl | rs1039571136 |
geneview | rs1039571136 |
scholar | rs1039571136 |
rs1039571136 | |
pharmgkb | rs1039571136 |
gwascentral | rs1039571136 |
openSNP | rs1039571136 |
23andMe | rs1039571136 |
SNPshot | rs1039571136 |
SNPdbe | rs1039571136 |
MSV3d | rs1039571136 |
GWAS Ctlg | rs1039571136 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1039571136(A;A) |
Alt | rs1039571136(A;A) |
Reference | Rs1039571136(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DYRK1A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.38862744C>T |
CLNSRC | |
CLNACC | RCV000438308.1, |