NCAN
neurocan
Summary
Neurocan is a chondroitin sulfate proteoglycan thought to be involved in the modulation of cell adhesion and migration.[supplied by OMIM, Jul 2002]
Known Variants97 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150057262 | 19:19,320,825 | C/G | upstream gene variant | — |
| rs1226557075 | 19:19,329,726 | A/G | — | uncertain significance |
| rs201014766 | 19:19,329,739 | C/A | — | uncertain significance |
| rs142344903 | 19:19,329,741 | G/A | — | uncertain significance |
| rs775167754 | 19:19,329,767 | G/A | — | uncertain significance |
| rs752908137 | 19:19,329,895 | G/A | — | uncertain significance |
| rs200876851 | 19:19,329,901 | C/T | — | uncertain significance |
| rs371203816 | 19:19,329,913 | G/A | — | uncertain significance |
| rs2228603 | 19:19,329,924 | C/A | missense variant | — |
| rs758661303 | 19:19,329,972 | C/A | — | uncertain significance |
| rs772797830 | 19:19,330,009 | G/A | — | uncertain significance |
| rs73537469 | 19:19,330,022 | G/A | — | benign |
| rs750535585 | 19:19,330,110 | C/G | — | uncertain significance |
| rs781045812 | 19:19,334,856 | C/T | — | uncertain significance |
| rs370349783 | 19:19,334,907 | A/G | — | uncertain significance |
| rs755850580 | 19:19,334,989 | C/T | — | uncertain significance |
| rs748873332 | 19:19,334,994 | C/T | — | uncertain significance |
| rs2512889407 | 19:19,335,125 | A/G | — | uncertain significance |
| rs760694042 | 19:19,335,240 | G/T | — | uncertain significance |
| rs774013427 | 19:19,335,849 | G/T | — | uncertain significance |
| rs762347973 | 19:19,335,975 | G/T | — | uncertain significance |
| rs1048789582 | 19:19,336,016 | C/T | — | uncertain significance |
| rs373616614 | 19:19,337,309 | T/C | — | likely benign |
| rs760043368 | 19:19,337,351 | G/T | — | uncertain significance |
| rs756020805 | 19:19,337,391 | T/C | — | uncertain significance |
| rs2060838050 | 19:19,337,424 | C/T | — | uncertain significance |
| rs763430819 | 19:19,337,568 | G/T | — | uncertain significance |
| rs758282635 | 19:19,337,607 | C/A | — | uncertain significance |
| rs368050420 | 19:19,337,732 | A/T | — | likely benign |
| rs767423304 | 19:19,337,756 | A/G | — | uncertain significance |
| rs760345363 | 19:19,337,835 | G/A | — | likely benign |
| rs541204872 | 19:19,337,872 | G/A | — | uncertain significance |
| rs757496531 | 19:19,338,155 | A/G | — | uncertain significance |
| rs137981080 | 19:19,338,212 | G/A | — | uncertain significance |
| rs145802020 | 19:19,338,242 | T/C | — | uncertain significance |
| rs748897933 | 19:19,338,417 | C/A | — | uncertain significance |
| rs1488052583 | 19:19,338,530 | C/T | — | uncertain significance |
| rs763105892 | 19:19,338,554 | G/A | — | uncertain significance |
| rs764118796 | 19:19,338,560 | A/G | — | uncertain significance |
| rs751676507 | 19:19,338,564 | G/A | — | uncertain significance |
| rs758158777 | 19:19,338,632 | G/A | — | uncertain significance |
| rs368061805 | 19:19,338,684 | G/T | — | uncertain significance |
| rs773199885 | 19:19,338,779 | T/C | — | uncertain significance |
| rs1433331786 | 19:19,338,803 | G/C | — | likely benign |
| rs2512894242 | 19:19,338,855 | A/G | — | uncertain significance |
| rs147095049 | 19:19,338,933 | C/T | — | likely benign |
| rs772683080 | 19:19,338,992 | G/A | — | uncertain significance |
| rs145824706 | 19:19,339,041 | C/T | — | uncertain significance |
| rs1284582050 | 19:19,339,043 | C/G | — | uncertain significance |
| rs148196919 | 19:19,339,050 | C/T | — | uncertain significance |
| rs1397789036 | 19:19,339,127 | G/A | — | uncertain significance |
| rs1349729567 | 19:19,339,161 | C/T | — | likely benign |
| rs373226707 | 19:19,339,179 | C/T | — | uncertain significance |
| rs372731221 | 19:19,339,269 | G/A | — | uncertain significance |
| rs138103127 | 19:19,339,284 | C/T | — | uncertain significance |
| rs139628713 | 19:19,339,330 | G/T | — | uncertain significance |
| rs748635441 | 19:19,339,440 | C/T | — | uncertain significance |
| rs746076521 | 19:19,344,616 | A/G | — | uncertain significance |
| rs773084164 | 19:19,344,655 | A/G | — | uncertain significance |
| rs199741597 | 19:19,344,692 | C/T | — | benign |
| rs146011974 | 19:19,344,693 | G/A | — | uncertain significance |
| rs201057751 | 19:19,344,696 | G/A | — | uncertain significance |
| rs746282362 | 19:19,344,712 | T/C | — | uncertain significance |
| rs374113750 | 19:19,345,806 | C/T | — | uncertain significance |
| rs1344343159 | 19:19,345,888 | G/A | — | uncertain significance |
| rs200250416 | 19:19,349,079 | C/T | — | uncertain significance |
| rs372133867 | 19:19,349,113 | G/A | — | uncertain significance |
| rs2060889691 | 19:19,349,148 | G/A | — | uncertain significance |
| rs1198462359 | 19:19,349,161 | G/A | — | uncertain significance |
| rs777170009 | 19:19,349,166 | C/T | — | uncertain significance |
| rs766345779 | 19:19,351,429 | A/T | — | uncertain significance |
| rs755692070 | 19:19,351,466 | A/C | — | uncertain significance |
| rs748590275 | 19:19,351,489 | G/A | — | uncertain significance |
| rs4353576 | 19:19,351,656 | C/T | intron variant | — |
| rs56352336 | 19:19,352,155 | T/G | — | — |
| rs182235102 | 19:19,353,270 | G/A | intron variant | — |
| rs114674887 | 19:19,355,485 | C/T | intron variant | — |
| rs1349079774 | 19:19,356,128 | G/C | — | uncertain significance |
| rs200706867 | 19:19,356,198 | A/T | — | uncertain significance |
| rs771319202 | 19:19,356,205 | C/A | — | uncertain significance |
| rs150818380 | 19:19,356,206 | G/A | — | uncertain significance |
| rs2512913273 | 19:19,356,242 | C/T | — | uncertain significance |
| rs111444407 | 19:19,358,207 | C/T | intron variant | — |
| rs555344889 | 19:19,359,529 | G/A | — | uncertain significance |
| rs755052570 | 19:19,359,553 | G/A | — | uncertain significance |
| rs145649413 | 19:19,359,572 | A/T | — | uncertain significance |
| rs1209194408 | 19:19,359,586 | A/C | — | uncertain significance |
| rs2512917425 | 19:19,359,626 | A/T | — | uncertain significance |
| rs761129840 | 19:19,359,686 | C/T | — | uncertain significance |
| rs2512917505 | 19:19,359,689 | A/G | — | uncertain significance |
| rs763221106 | 19:19,360,580 | C/T | — | uncertain significance |
| rs764284962 | 19:19,360,581 | G/A | — | uncertain significance |
| rs74942769 | 19:19,360,582 | T/G | — | benign |
| rs375941465 | 19:19,360,595 | C/T | — | uncertain significance |
| rs112069465 | 19:19,360,618 | A/T | — | likely benign |
| rs201770310 | 19:19,360,703 | G/A | — | uncertain significance |
| rs1064395 | 19:19,361,735 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.