DCC
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | DCC netrin 1 receptor |
| EntrezGene | 1630 |
| PheGenI | 1630 |
| VariationViewer | 1630 |
| ClinVar | DCC |
| GeneCards | DCC |
| dbSNP | 1630 |
| Diseases | DCC |
| SADR | 1630 |
| HugeNav | 1630 |
| wikipedia | DCC |
| DCC | |
| gopubmed | DCC |
| EVS | DCC |
| HEFalMp | DCC |
| MyGene2 | DCC |
| 23andMe | DCC |
| UniProt | P43146 |
| Ensembl | ENSG00000187323 |
| OMIM | 120470 |
| # SNPs | 32 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs10502974 | 0 | 53,411,491 | |
| rs1057519053 | 0 | 52,925,310 | |
| rs1057519054 | 0 | 53,386,061 | |
| rs1057519055 | 0 | 53,386,097 | |
| rs1057519056 | 0 | 53,207,746 | |
| rs1057519057 | 0 | 53,391,876 | |
| rs1057519058 | 0 | 53,467,923 | |
| rs1085307773 | 0 | 53,207,745 | |
| rs11876941 | 0 | 53,379,661 | |
| rs121912967 | 0 | 52,906,134 | |
| rs1460196 | 0 | 52,689,042 | |
| rs17468382 | 0 | 52,734,641 | |
| rs199651452 | 0 | 53,339,775 | |
| rs2229080 | 0 | 52,906,232 | |
| rs2270954 | 2 | 53,530,928 | |
| rs387906555 | 0 | 53,526,629 | |
| rs4078288 | 0 | 53,020,881 | |
| rs4940203 | 0 | 52,666,026 | |
| rs714 | 0 | 52,992,904 | |
| rs748112308 | 0 | 53,486,808 | |
| rs7504990 | 0 | 52,991,406 | |
| rs754914260 | 0 | 52,923,832 | |
| rs768048 | 0 | 52,759,028 | |
| rs775565634 | 0 | 53,339,808 | |
| rs797044551 | 0 | 52,752,339 | |
| rs797044552 | 0 | 52,906,202 | |
| rs797044553 | 0 | 53,063,460 | |
| rs797044554 | 0 | 53,157,430 | |
| rs797044555 | 0 | 53,402,833 | |
| rs797044556 | 0 | 53,486,895 | |
| rs9944880 | 0 | 53,125,996 | |
| rs9951523 | 0 | 52,340,854 |
[PMID 25607358] Common genetic variants influence human subcortical brain structures.
[PMID 28250456] Biallelic mutations in human DCC cause developmental split-brain syndrome
