| IMS-JST186502 | |
| JSNP ID | IMS-JST186502 |
| Chromosome | 12 |
| Location | 12p13 |
| Evidence of Location | EntrezGene ID 3822 |
| In Gene | intron*3 |
| Type | SNP |
| Frequencies | 0.00 0.00 0.500 |
| allele | G/C |
| dbSNP ss# | 5011775 |
| dbSNP rs# | 3825294 |
| HGVBase-ID | SNP002315147 |
| 5' assay | TAATTCAAGGTGAAAAACGAGCCAAAATATAAACTATGTTTAAGGATTTCTTAGAGTATT |
| 3' assay | ACATCATTGCCGCTGGAGAATCACTCAAG |
| Mapping Accession | NT_009714.17;NT_009714.17 |
| Mapping Position | 3334808;3350232 |
| Mapping Symbol | KLRC3 NKG2-E;KLRC2 NKG2-E |
| Mapping OMIM-ID | 602892;602891 |
| Screened Accession | NT_009701.1 |
| Screened Position | 962917 |
| Screened Symbol | KLRC2 |
| Screened OMIM-ID | - |