rs2991216
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2991216(C;C) |
Make rs2991216(C;T) |
Make rs2991216(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 90865745 |
Gene | SYK |
is a | snp |
is | mentioned by |
dbSNP | rs2991216 |
dbSNP (classic) | rs2991216 |
ClinGen | rs2991216 |
ebi | rs2991216 |
HLI | rs2991216 |
Exac | rs2991216 |
Gnomad | rs2991216 |
Varsome | rs2991216 |
LitVar | rs2991216 |
Map | rs2991216 |
PheGenI | rs2991216 |
Biobank | rs2991216 |
1000 genomes | rs2991216 |
hgdp | rs2991216 |
ensembl | rs2991216 |
geneview | rs2991216 |
scholar | rs2991216 |
rs2991216 | |
pharmgkb | rs2991216 |
gwascentral | rs2991216 |
openSNP | rs2991216 |
23andMe | rs2991216 |
SNPshot | rs2991216 |
SNPdbe | rs2991216 |
MSV3d | rs2991216 |
GWAS Ctlg | rs2991216 |
GMAF | 0.2066 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21148756] Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma