rs6509940
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6509940(C;C) |
Make rs6509940(C;T) |
Make rs6509940(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 55372511 |
is a | snp |
is | mentioned by |
dbSNP | rs6509940 |
dbSNP (classic) | rs6509940 |
ClinGen | rs6509940 |
ebi | rs6509940 |
HLI | rs6509940 |
Exac | rs6509940 |
Gnomad | rs6509940 |
Varsome | rs6509940 |
LitVar | rs6509940 |
Map | rs6509940 |
PheGenI | rs6509940 |
Biobank | rs6509940 |
1000 genomes | rs6509940 |
hgdp | rs6509940 |
ensembl | rs6509940 |
geneview | rs6509940 |
scholar | rs6509940 |
rs6509940 | |
pharmgkb | rs6509940 |
gwascentral | rs6509940 |
openSNP | rs6509940 |
23andMe | rs6509940 |
SNPshot | rs6509940 |
SNPdbe | rs6509940 |
MSV3d | rs6509940 |
GWAS Ctlg | rs6509940 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26172388] Genetic variants of IL-11 associated with risk of Hirschsprung disease