rs1088967
From SNPedia
Merged into | rs204340 |
Orientation | minus |
Stabilized | minus |
Make rs1088967(A;A) |
Make rs1088967(A;G) |
Make rs1088967(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | X |
Position | 127010099 |
is a | snp |
is | mentioned by |
dbSNP | rs1088967 |
dbSNP (classic) | rs1088967 |
ClinGen | rs1088967 |
ebi | rs1088967 |
HLI | rs1088967 |
Exac | rs1088967 |
Gnomad | rs1088967 |
Varsome | rs1088967 |
LitVar | rs1088967 |
Map | rs1088967 |
PheGenI | rs1088967 |
Biobank | rs1088967 |
1000 genomes | rs1088967 |
hgdp | rs1088967 |
ensembl | rs1088967 |
geneview | rs1088967 |
scholar | rs1088967 |
rs1088967 | |
pharmgkb | rs1088967 |
gwascentral | rs1088967 |
openSNP | rs1088967 |
23andMe | rs1088967 |
SNPshot | rs1088967 |
SNPdbe | rs1088967 |
MSV3d | rs1088967 |
GWAS Ctlg | rs1088967 |
Status | Merged into rs204340 |
Max Magnitude | 0 |
[PMID 25680555] Interleukin-17FT7488 allele is associated with a decreased risk of colorectal cancer and tumor progression