{{Rsnum
|rsid=2617170
|Gene=KLRC4
|Chromosome=12
|position=10408358
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.4017
|Gene_s=KLRC4,KLRC4-KLRK1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 50.0 | 43.8 | 6.2
| HCB | 42.2 | 35.6 | 22.2
| JPT | 50.0 | 34.1 | 15.9
| YRI | 21.4 | 52.4 | 26.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 42.2 | 35.6 | 22.2
| CHD | 21.9 | 55.2 | 22.9
| GIH | 0.0 | 0.0 | 0.0
| LWK | 12.3 | 57.5 | 30.2
| MEX | 0.0 | 0.0 | 0.0
| MKK | 22.2 | 52.3 | 25.5
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}This SNP is part of a haplotype reported for the [[KLRK1]] gene, potentially associated with risk for [[colorectal cancer]]; see details at [[rs1049174]].

{{ neighbor
| rsid = 2617171
| distance = 322
}}

{{PMID Auto
|PMID=20648603
|Title=Association of NKG2D genetic polymorphism with susceptibility to chronic hepatitis B in a Han Chinese population
}}

{{GET Evidence
|gene=KLRC4
|aa_change=Asn104Ser
|aa_change_short=N104S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2617170
|overall_frequency_n=6540
|overall_frequency_d=10730
|overall_frequency=0.609506
|n_genomes=41
|n_genomes_annotated=0
|n_haplomes=63
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{PMID Auto GWAS
  |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.
  |RiskAllele=T
  |Pval=1E-9
  |OR=1.28
  |ORtxt=[1.18-1.39]
  |OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}