C12orf42
chromosome 12 open reading frame 42
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1850956 | 12:103,453,387 | T/C | intergenic variant | — |
| rs4584635 | 12:103,475,044 | A/C | coding sequence variant | — |
| rs10745954 | 12:103,483,094 | A/C | — | — |
| rs10778213 | 12:103,495,151 | T/G | — | — |
| rs4764723 | 12:103,512,304 | C/T | upstream gene variant | — |
| rs4764724 | 12:103,512,307 | T/G | upstream gene variant | — |
| rs4764725 | 12:103,512,314 | T/G | — | — |
| rs4764726 | 12:103,512,325 | C/G | upstream gene variant | — |
| rs11525595 | 12:103,529,846 | A/T | intron variant | — |
| rs10778215 | 12:103,537,266 | T/A | intron variant | — |
| rs12300756 | 12:103,541,943 | C/T | upstream gene variant | — |
| rs10860960 | 12:103,594,062 | C/T | intergenic variant | — |
| rs10860964 | 12:103,596,455 | T/C | intergenic variant | — |
| rs184768787 | 12:103,608,322 | C/T | intergenic variant | — |
| rs190368447 | 12:103,627,723 | A/G | downstream gene variant | — |
| rs765148696 | 12:103,699,796 | G/T | — | uncertain significance |
| rs6419384 | 12:103,705,098 | T/A | — | — |
| rs6539064 | 12:103,706,754 | C/G | intron variant | — |
| rs182543447 | 12:103,711,067 | C/G | intron variant | — |
| rs202037943 | 12:103,715,281 | C/T | — | — |
| rs73185857 | 12:103,720,658 | C/A | intron variant | — |
| rs7969447 | 12:103,762,097 | A/T | — | — |
| rs112545586 | 12:103,795,426 | T/G | — | likely benign |
| rs200782771 | 12:103,795,431 | A/T | — | uncertain significance |
| rs144387465 | 12:103,893,218 | A/C | upstream gene variant | — |
| rs10861032 | 12:103,912,506 | T/G | — | — |
| rs149580590 | 12:103,929,821 | A/G | intergenic variant | — |
| rs56023569 | 12:103,937,666 | T/G | — | — |
| rs190947296 | 12:103,948,893 | G/T | intron variant | — |
| rs186824649 | 12:103,959,058 | G/A | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.