CLEC16A
C-type lectin domain containing 16A
Summary
This gene encodes a member of the C-type lectin domain containing family. Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
Known Variants125 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs756014800 | 16:11,038,620 | A/G | — | uncertain significance |
| rs199548274 | 16:11,051,651 | C/T | — | likely benign |
| rs1252394661 | 16:11,051,691 | A/C | — | uncertain significance |
| rs200973931 | 16:11,056,326 | A/G | — | uncertain significance |
| rs7188928 | 16:11,058,753 | C/A | regulatory region variant | — |
| rs201136444 | 16:11,066,802 | C/A | — | uncertain significance |
| rs2506170500 | 16:11,066,803 | C/G | — | uncertain significance |
| rs1434028977 | 16:11,066,804 | A/C | — | uncertain significance |
| rs2506379070 | 16:11,071,110 | C/G | — | uncertain significance |
| rs200900880 | 16:11,071,147 | A/G | — | uncertain significance |
| rs200877970 | 16:11,071,164 | A/C | — | uncertain significance |
| rs2506385343 | 16:11,071,188 | C/T | — | uncertain significance |
| rs1036186905 | 16:11,073,190 | G/A | — | uncertain significance |
| rs74163607 | 16:11,073,195 | C/T | — | uncertain significance |
| rs2506755594 | 16:11,076,738 | T/G | — | uncertain significance |
| rs1172084881 | 16:11,076,759 | C/A | — | uncertain significance |
| rs200192513 | 16:11,076,828 | C/G | — | uncertain significance |
| rs6498142 | 16:11,081,249 | C/G | intron variant | — |
| rs370740805 | 16:11,096,932 | C/T | — | uncertain significance |
| rs775920891 | 16:11,096,947 | G/A | — | uncertain significance |
| rs2507534780 | 16:11,096,971 | C/T | — | uncertain significance |
| rs74163611 | 16:11,096,980 | G/A | — | uncertain significance |
| rs201074148 | 16:11,097,016 | G/A | — | uncertain significance |
| rs200082818 | 16:11,097,146 | G/A | — | likely benign |
| rs45464291 | 16:11,097,155 | G/A | — | likely benign |
| rs9925481 | 16:11,097,479 | C/G | — | — |
| rs17804470 | 16:11,099,968 | G/A | — | — |
| rs1262017214 | 16:11,114,067 | A/G | — | uncertain significance |
| rs2508413288 | 16:11,114,076 | A/G | — | uncertain significance |
| rs200731011 | 16:11,114,098 | C/G | — | uncertain significance |
| rs201325973 | 16:11,114,114 | G/C | — | uncertain significance |
| rs74163614 | 16:11,114,170 | C/T | — | likely benign |
| rs2286974 | 16:11,114,512 | A/C | — | — |
| rs1459928423 | 16:11,118,706 | C/A | — | uncertain significance |
| rs769941408 | 16:11,118,731 | A/G | — | uncertain significance |
| rs202155030 | 16:11,118,742 | G/A | — | uncertain significance |
| rs764829700 | 16:11,118,758 | A/G | — | uncertain significance |
| rs749832710 | 16:11,118,767 | C/G | — | uncertain significance |
| rs71381188 | 16:11,129,243 | G/T | intron variant | — |
| rs374390774 | 16:11,133,629 | T/C | — | uncertain significance |
| rs199576357 | 16:11,133,686 | C/T | — | likely benign |
| rs780206082 | 16:11,133,721 | G/A | — | uncertain significance |
| rs2047225767 | 16:11,133,731 | C/A | — | uncertain significance |
| rs866629699 | 16:11,136,129 | C/T | — | uncertain significance |
| rs763777406 | 16:11,136,132 | C/T | — | uncertain significance |
| rs201983240 | 16:11,136,149 | C/G | — | uncertain significance |
| rs759379466 | 16:11,136,175 | G/A | — | uncertain significance |
| rs750171153 | 16:11,137,916 | G/A | — | uncertain significance |
| rs780853392 | 16:11,141,186 | A/G | — | uncertain significance |
| rs372722698 | 16:11,145,442 | A/T | — | uncertain significance |
| rs200827060 | 16:11,145,457 | G/A | — | uncertain significance |
| rs201963363 | 16:11,154,762 | A/G | — | uncertain significance |
| rs192909138 | 16:11,154,816 | G/A | — | uncertain significance |
| rs781571686 | 16:11,154,829 | C/T | — | uncertain significance |
| rs1175413524 | 16:11,154,836 | T/G | — | likely benign |
| rs887864 | 16:11,158,885 | G/C | — | — |
| rs11865121 | 16:11,166,688 | C/T | — | — |
| rs725613 | 16:11,169,683 | T/G | upstream gene variant | — |
| rs2041670 | 16:11,174,652 | G/C | — | — |
| rs11648679 | 16:11,175,984 | A/G | intron variant | — |
| rs7200786 | 16:11,177,801 | A/T | — | — |
| rs12708715 | 16:11,177,824 | C/T | intron variant | — |
| rs12708716 | 16:11,179,873 | A/G | intron variant | — |
| rs12926153 | 16:11,180,762 | C/G | intron variant | — |
| rs12924729 | 16:11,187,783 | G/A | intron variant | — |
| rs12917716 | 16:11,189,148 | G/A | — | — |
| rs7205916 | 16:11,189,256 | C/A | intron variant | — |
| rs12599402 | 16:11,189,888 | T/C | intron variant | — |
| rs17806056 | 16:11,192,499 | T/A | intron variant | — |
| rs34972832 | 16:11,198,938 | G/T | — | — |
| rs998592 | 16:11,199,678 | C/T | regulatory region variant | — |
| rs12923054 | 16:11,202,738 | C/G | — | — |
| rs12924985 | 16:11,208,322 | G/C | intron variant | — |
| rs9923856 | 16:11,210,415 | T/C | intron variant | — |
| rs2080272 | 16:11,211,553 | A/C | — | — |
| rs1460716883 | 16:11,214,583 | G/T | — | uncertain significance |
| rs34306440 | 16:11,215,035 | A/C | — | — |
| rs2510674494 | 16:11,217,621 | A/T | — | uncertain significance |
| rs377523777 | 16:11,217,626 | G/A | — | uncertain significance |
| rs1465122889 | 16:11,217,641 | A/C | — | uncertain significance |
| rs201484643 | 16:11,217,650 | A/G | — | uncertain significance |
| rs765317406 | 16:11,217,780 | G/T | — | uncertain significance |
| rs8064154 | 16:11,219,419 | A/G | intron variant | — |
| rs200280529 | 16:11,219,888 | C/T | — | likely benign |
| rs201467931 | 16:11,219,889 | G/A | — | uncertain significance |
| rs761303559 | 16:11,219,922 | C/T | — | uncertain significance |
| rs2510708241 | 16:11,219,936 | G/T | — | uncertain significance |
| rs375812913 | 16:11,219,944 | G/A | — | uncertain significance |
| rs749475348 | 16:11,219,949 | A/G | — | uncertain significance |
| rs2510708904 | 16:11,219,956 | A/T | — | uncertain significance |
| rs200156002 | 16:11,219,976 | G/A | — | uncertain significance |
| rs2510709534 | 16:11,219,993 | C/G | — | uncertain significance |
| rs78394940 | 16:11,222,238 | C/T | intron variant | — |
| rs556852922 | 16:11,224,643 | C/G | — | — |
| rs2241099 | 16:11,225,064 | C/G | regulatory region variant | — |
| rs62026376 | 16:11,228,712 | C/T | intron variant | — |
| rs2041733 | 16:11,229,589 | T/G | — | — |
| rs7203459 | 16:11,230,703 | T/C | regulatory region variant | — |
| rs2903692 | 16:11,238,783 | G/A | intron variant | — |
| rs17673553 | 16:11,241,906 | A/G | intron variant | — |
Showing 100 of 125 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.