| IMS-JST007093 | |
| JSNP ID | IMS-JST007093 |
| Chromosome | 17 |
| Location | 17q21.2 |
| Evidence of Location | EntrezGene ID 3882 |
| In Gene | CDS*3 |
| Type | SNP |
| Frequencies | 0.00 0.00 0.149 0.178 0.196 0.217 0.333 0.352 0.383 0.4152 0.416 0.422 0.435 0.438 0.467 0.467 0.494 0.500 0.500 0.500 0.500 |
| allele | C/A |
| dbSNP ss# | 2985222 |
| dbSNP rs# | 2071561 |
| HGVBase-ID | SNP000572190 |
| 5' assay | TGCGCAGGATCCTGGATGATCTCACTCTGTGCAAGGCTGACCTGGAGGCCCAGGTTGAGT |
| 3' assay | CCTGAAGGAGGAGCTGATGTGCCTCAAAAAGAACCATGAGGAGGTGAGGCTGGAAGTCCC |
| Mapping Accession | NT_010783.15 |
| Mapping Position | 4896220 |
| Mapping Symbol | KRT32 |
| Mapping OMIM-ID | 602760 |
| Screened Accession | X90761.1 |
| Screened Position | 6090 |
| Screened Symbol | hHa2 |
| Screened OMIM-ID | - |