CCDC150
coiled-coil domain containing 150
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1692093522 | 2:197,504,495 | A/T | — | uncertain significance |
| rs753502575 | 2:197,511,093 | C/T | — | uncertain significance |
| rs372552459 | 2:197,511,095 | G/A | — | uncertain significance |
| rs200183130 | 2:197,511,096 | T/C | — | uncertain significance |
| rs890864456 | 2:197,521,358 | G/T | — | uncertain significance |
| rs202212006 | 2:197,521,415 | C/T | — | uncertain significance |
| rs370426343 | 2:197,521,437 | G/A | — | uncertain significance |
| rs554218636 | 2:197,521,468 | C/A | — | uncertain significance |
| rs758763208 | 2:197,521,550 | G/A | — | uncertain significance |
| rs368606812 | 2:197,521,551 | A/G | — | uncertain significance |
| rs769775155 | 2:197,521,799 | A/G | — | uncertain significance |
| rs561326085 | 2:197,521,817 | T/G | — | uncertain significance |
| rs371236615 | 2:197,521,831 | G/T | — | uncertain significance |
| rs750855228 | 2:197,521,834 | A/G | — | uncertain significance |
| rs1412291794 | 2:197,523,528 | A/G | — | uncertain significance |
| rs34638305 | 2:197,523,550 | C/G | — | uncertain significance |
| rs568066863 | 2:197,530,402 | A/C | — | uncertain significance |
| rs753442017 | 2:197,531,477 | G/A | — | likely benign |
| rs745935158 | 2:197,531,521 | A/C | — | likely benign |
| rs1400127156 | 2:197,531,542 | A/C | — | uncertain significance |
| rs866322960 | 2:197,531,561 | A/C | — | uncertain significance |
| rs539785078 | 2:197,537,153 | A/G | — | uncertain significance |
| rs1694367651 | 2:197,539,007 | T/G | — | uncertain significance |
| rs747685162 | 2:197,539,010 | A/G | — | uncertain significance |
| rs568201168 | 2:197,539,046 | A/G | — | uncertain significance |
| rs2468735091 | 2:197,540,979 | T/C | — | uncertain significance |
| rs375520178 | 2:197,540,985 | C/A | — | uncertain significance |
| rs754768005 | 2:197,541,298 | A/G | — | uncertain significance |
| rs1033214898 | 2:197,541,342 | G/A | — | uncertain significance |
| rs2468737201 | 2:197,541,375 | G/C | — | uncertain significance |
| rs374012147 | 2:197,542,021 | A/C | — | uncertain significance |
| rs1248340811 | 2:197,559,804 | C/T | — | uncertain significance |
| rs199761560 | 2:197,559,839 | A/C | — | uncertain significance |
| rs1695740532 | 2:197,559,851 | G/C | — | uncertain significance |
| rs1363291112 | 2:197,565,885 | A/G | — | uncertain significance |
| rs184775562 | 2:197,569,112 | T/C | intron variant | — |
| rs777382954 | 2:197,576,893 | C/A | — | uncertain significance |
| rs781005190 | 2:197,576,927 | A/G | — | uncertain significance |
| rs774671380 | 2:197,576,938 | C/T | — | uncertain significance |
| rs112081371 | 2:197,577,455 | C/G | — | uncertain significance |
| rs138410566 | 2:197,583,281 | C/T | — | uncertain significance |
| rs771970184 | 2:197,584,331 | G/C | — | uncertain significance |
| rs753108186 | 2:197,584,354 | G/A | — | uncertain significance |
| rs945609225 | 2:197,586,343 | A/G | — | uncertain significance |
| rs1484622951 | 2:197,586,355 | A/T | — | uncertain significance |
| rs1395972631 | 2:197,590,809 | C/T | — | uncertain significance |
| rs773160673 | 2:197,590,810 | G/A | — | uncertain significance |
| rs2468947407 | 2:197,593,946 | C/A | — | uncertain significance |
| rs201155897 | 2:197,593,965 | C/T | — | uncertain significance |
| rs767812568 | 2:197,593,996 | C/T | — | uncertain significance |
| rs369618402 | 2:197,594,538 | C/A | — | uncertain significance |
| rs756721613 | 2:197,594,569 | A/G | — | uncertain significance |
| rs1395245506 | 2:197,594,577 | T/C | — | uncertain significance |
| rs777158804 | 2:197,594,704 | G/A | — | likely benign |
| rs373923133 | 2:197,594,772 | G/A | — | uncertain significance |
| rs376127384 | 2:197,594,775 | A/G | — | uncertain significance |
| rs374003366 | 2:197,594,807 | C/T | — | uncertain significance |
| rs201604646 | 2:197,594,834 | C/T | — | uncertain significance |
| rs781411346 | 2:197,595,617 | G/A | — | uncertain significance |
| rs1172934313 | 2:197,597,195 | T/C | — | uncertain significance |
| rs2468963286 | 2:197,597,204 | A/G | — | uncertain significance |
| rs556018318 | 2:197,597,237 | A/G | — | uncertain significance |
| rs879650586 | 2:197,597,251 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.