rs1943950
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1943950(C;C) |
Make rs1943950(C;T) |
Make rs1943950(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 30107534 |
is a | snp |
is | mentioned by |
dbSNP | rs1943950 |
dbSNP (classic) | rs1943950 |
ClinGen | rs1943950 |
ebi | rs1943950 |
HLI | rs1943950 |
Exac | rs1943950 |
Gnomad | rs1943950 |
Varsome | rs1943950 |
LitVar | rs1943950 |
Map | rs1943950 |
PheGenI | rs1943950 |
Biobank | rs1943950 |
1000 genomes | rs1943950 |
hgdp | rs1943950 |
ensembl | rs1943950 |
geneview | rs1943950 |
scholar | rs1943950 |
rs1943950 | |
pharmgkb | rs1943950 |
gwascentral | rs1943950 |
openSNP | rs1943950 |
23andMe | rs1943950 |
SNPshot | rs1943950 |
SNPdbe | rs1943950 |
MSV3d | rs1943950 |
GWAS Ctlg | rs1943950 |
GMAF | 0.1919 |
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