{{Rsnum
|rsid=9469003
|Gene=MICA
|Chromosome=6
|position=31440051
|Orientation=plus
|GMAF=0.2406
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LINC01149
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 23.0 | 75.2
| HCB | 4.4 | 27.0 | 68.6
| JPT | 3.5 | 20.4 | 76.1
| YRI | 15.0 | 42.2 | 42.9
| ASW | 12.3 | 49.1 | 38.6
| CHB | 4.4 | 27.0 | 68.6
| CHD | 0.9 | 27.5 | 71.6
| GIH | 8.9 | 48.5 | 42.6
| LWK | 15.5 | 43.6 | 40.9
| MEX | 8.8 | 31.6 | 59.6
| MKK | 7.1 | 36.5 | 56.4
| TSI | 2.0 | 33.3 | 64.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21801394
|Trait=None
|Title=Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
|RiskAllele=C
|Pval=2E-9
|OR=1.7300
|ORtxt=[1.44-2.08]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}