rs2617170
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | Normal |
Make rs2617170(C;T) |
Make rs2617170(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 10408358 |
Gene | KLRC4, KLRC4-KLRK1 |
is a | snp |
is | mentioned by |
dbSNP | rs2617170 |
dbSNP (classic) | rs2617170 |
ClinGen | rs2617170 |
ebi | rs2617170 |
HLI | rs2617170 |
Exac | rs2617170 |
Gnomad | rs2617170 |
Varsome | rs2617170 |
LitVar | rs2617170 |
Map | rs2617170 |
PheGenI | rs2617170 |
Biobank | rs2617170 |
1000 genomes | rs2617170 |
hgdp | rs2617170 |
ensembl | rs2617170 |
geneview | rs2617170 |
scholar | rs2617170 |
rs2617170 | |
pharmgkb | rs2617170 |
gwascentral | rs2617170 |
openSNP | rs2617170 |
23andMe | rs2617170 |
SNPshot | rs2617170 |
SNPdbe | rs2617170 |
MSV3d | rs2617170 |
GWAS Ctlg | rs2617170 |
GMAF | 0.4017 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
This SNP is part of a haplotype reported for the KLRK1 gene, potentially associated with risk for colorectal cancer; see details at rs1049174.
[PMID 20648603] Association of NKG2D genetic polymorphism with susceptibility to chronic hepatitis B in a Han Chinese population
GWAS snp | |
---|---|
PMID | [PMID 23291587] |
Trait | Behcet's disease |
Title | Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. |
Risk Allele | T |
P-val | 1E-9 |
Odds Ratio | 1.28 [1.18-1.39] |