rs2832616
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2832616(C;C) |
Make rs2832616(C;T) |
Make rs2832616(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 30101474 |
is a | snp |
is | mentioned by |
dbSNP | rs2832616 |
dbSNP (classic) | rs2832616 |
ClinGen | rs2832616 |
ebi | rs2832616 |
HLI | rs2832616 |
Exac | rs2832616 |
Gnomad | rs2832616 |
Varsome | rs2832616 |
LitVar | rs2832616 |
Map | rs2832616 |
PheGenI | rs2832616 |
Biobank | rs2832616 |
1000 genomes | rs2832616 |
hgdp | rs2832616 |
ensembl | rs2832616 |
geneview | rs2832616 |
scholar | rs2832616 |
rs2832616 | |
pharmgkb | rs2832616 |
gwascentral | rs2832616 |
openSNP | rs2832616 |
23andMe | rs2832616 |
SNPshot | rs2832616 |
SNPdbe | rs2832616 |
MSV3d | rs2832616 |
GWAS Ctlg | rs2832616 |
GMAF | 0.1951 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23783273] The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome