rs2279398
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2279398(A;A) |
Make rs2279398(A;G) |
Make rs2279398(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 177503768 |
Gene | DOK3 |
is a | snp |
is | mentioned by |
dbSNP | rs2279398 |
dbSNP (classic) | rs2279398 |
ClinGen | rs2279398 |
ebi | rs2279398 |
HLI | rs2279398 |
Exac | rs2279398 |
Gnomad | rs2279398 |
Varsome | rs2279398 |
LitVar | rs2279398 |
Map | rs2279398 |
PheGenI | rs2279398 |
Biobank | rs2279398 |
1000 genomes | rs2279398 |
hgdp | rs2279398 |
ensembl | rs2279398 |
geneview | rs2279398 |
scholar | rs2279398 |
rs2279398 | |
pharmgkb | rs2279398 |
gwascentral | rs2279398 |
openSNP | rs2279398 |
23andMe | rs2279398 |
SNPshot | rs2279398 |
SNPdbe | rs2279398 |
MSV3d | rs2279398 |
GWAS Ctlg | rs2279398 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 27354594] Impact of Genetic Variation in MicroRNA-binding Site on Susceptibility to Colorectal Cancer.