NOS2
nitric oxide synthase 2
Summary
Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. This gene encodes a nitric oxide synthase which is expressed in liver and is inducible by a combination of lipopolysaccharide and certain cytokines. Three related pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Known Variants140 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7223110 | 17:26,084,326 | C/T | — | benign |
| rs1317211576 | 17:26,084,334 | A/G | — | uncertain significance |
| rs1567631042 | 17:26,084,339 | A/T | — | uncertain significance |
| rs11653716 | 17:26,084,532 | C/G | downstream gene variant | — |
| rs141730458 | 17:26,085,928 | C/T | — | likely benign |
| rs3729662 | 17:26,085,931 | G/A | — | benign |
| rs750641734 | 17:26,085,970 | C/T | — | likely benign |
| rs1908019475 | 17:26,085,980 | G/A | — | uncertain significance |
| rs201947529 | 17:26,085,996 | G/A | — | likely benign |
| rs113419464 | 17:26,086,005 | G/A | — | likely benign |
| rs202086662 | 17:26,086,026 | G/A | — | uncertain significance |
| rs774411653 | 17:26,086,030 | G/T | — | likely benign |
| rs139005303 | 17:26,086,063 | G/C | — | uncertain significance |
| rs375424266 | 17:26,087,075 | C/T | — | uncertain significance |
| rs377638076 | 17:26,087,081 | T/C | — | uncertain significance |
| rs1908064565 | 17:26,087,084 | G/A | — | uncertain significance |
| rs150061937 | 17:26,087,096 | G/A | — | uncertain significance |
| rs754624745 | 17:26,087,123 | T/G | — | uncertain significance |
| rs748014613 | 17:26,087,129 | A/G | — | uncertain significance |
| rs149201685 | 17:26,087,163 | G/T | — | likely benign |
| rs762167122 | 17:26,087,189 | C/T | — | uncertain significance |
| rs778756552 | 17:26,087,199 | G/A | — | uncertain significance |
| rs745804011 | 17:26,087,654 | T/A | — | uncertain significance |
| rs768716650 | 17:26,087,746 | C/G | — | uncertain significance |
| rs2255929 | 17:26,087,967 | T/C | — | — |
| rs200387756 | 17:26,088,160 | G/C | — | likely benign |
| rs140914849 | 17:26,088,203 | T/C | — | uncertain significance |
| rs753799387 | 17:26,088,231 | C/G | — | uncertain significance |
| rs3729507 | 17:26,088,432 | C/T | — | — |
| rs8068149 | 17:26,088,855 | G/A | intron variant | — |
| rs9906835 | 17:26,089,374 | A/G | intron variant | — |
| rs201282647 | 17:26,089,832 | T/A | — | uncertain significance |
| rs1060826 | 17:26,089,867 | T/C | synonymous variant | benign |
| rs200386224 | 17:26,089,883 | C/T | — | likely benign |
| rs767806769 | 17:26,089,884 | G/T | — | likely benign |
| rs1567633262 | 17:26,089,886 | G/C | — | uncertain significance |
| rs1323586844 | 17:26,089,955 | C/A | — | uncertain significance |
| rs2297510 | 17:26,090,754 | T/C | intron variant | — |
| rs528170673 | 17:26,091,090 | G/T | — | uncertain significance |
| rs202007638 | 17:26,091,178 | G/A | — | likely benign |
| rs2297511 | 17:26,091,227 | C/T | — | — |
| rs944722 | 17:26,092,037 | C/T | intron variant | — |
| rs28944178 | 17:26,092,552 | G/A | — | benign |
| rs2297512 | 17:26,092,555 | G/A | — | benign |
| rs1060822 | 17:26,092,631 | A/G | synonymous variant | benign |
| rs144057872 | 17:26,092,644 | G/A | — | likely benign |
| rs766007051 | 17:26,092,647 | G/A | — | uncertain significance |
| rs201105235 | 17:26,092,662 | C/A | — | likely benign |
| rs1597545487 | 17:26,092,667 | C/A | — | likely benign |
| rs1167154742 | 17:26,092,720 | G/C | — | uncertain significance |
| rs150704221 | 17:26,092,740 | C/T | — | uncertain significance |
| rs2297514 | 17:26,093,315 | T/C | intron variant | — |
| rs773949014 | 17:26,093,564 | G/A | — | uncertain significance |
| rs765612792 | 17:26,093,588 | C/T | — | uncertain significance |
| rs201789784 | 17:26,094,781 | G/A | — | uncertain significance |
| rs146852100 | 17:26,094,796 | T/C | — | likely benign |
| rs557447784 | 17:26,094,850 | G/A | — | uncertain significance |
| rs770773571 | 17:26,094,852 | C/T | — | likely benign |
| rs199536608 | 17:26,094,856 | C/T | — | uncertain significance |
| rs199861578 | 17:26,096,070 | A/G | — | likely benign |
| rs750027214 | 17:26,096,094 | A/T | — | uncertain significance |
| rs202098132 | 17:26,096,132 | G/A | — | likely benign |
| rs747176795 | 17:26,096,148 | A/G | — | uncertain significance |
| rs201137209 | 17:26,096,159 | G/A | — | likely benign |
| rs201500956 | 17:26,096,184 | G/A | — | likely benign |
| rs9282801 | 17:26,096,473 | C/A | intron variant | benign |
| rs2297518 | 17:26,096,597 | G/A | missense variant | benign |
| rs28999412 | 17:26,097,993 | C/G | — | likely benign |
| rs2274894 | 17:26,099,171 | T/A | — | — |
| rs3729720 | 17:26,099,324 | G/A | — | benign |
| rs1292564630 | 17:26,099,353 | C/T | — | uncertain significance |
| rs143226463 | 17:26,099,383 | G/A | — | uncertain significance |
| rs768467991 | 17:26,099,412 | G/A | — | likely benign |
| rs148070104 | 17:26,099,450 | G/C | — | uncertain significance |
| rs1567637005 | 17:26,100,205 | G/A | — | uncertain significance |
| rs201161495 | 17:26,100,237 | G/A | — | likely benign |
| rs886282449 | 17:26,100,251 | G/C | — | uncertain significance |
| rs2248814 | 17:26,100,321 | A/G | intron variant | benign |
| rs3729966 | 17:26,101,237 | A/G | — | benign |
| rs201695469 | 17:26,101,298 | A/G | — | likely benign |
| rs200787576 | 17:26,101,310 | G/A | — | likely benign |
| rs200193371 | 17:26,101,386 | G/A | — | uncertain significance |
| rs762375822 | 17:26,101,399 | G/A | — | uncertain significance |
| rs112588673 | 17:26,101,404 | C/T | — | uncertain significance |
| rs137979503 | 17:26,101,405 | G/A | — | uncertain significance |
| rs979042320 | 17:26,105,724 | T/C | — | uncertain significance |
| rs1908739723 | 17:26,105,741 | T/C | — | uncertain significance |
| rs139794069 | 17:26,105,754 | C/T | — | uncertain significance |
| rs776131561 | 17:26,105,792 | T/G | — | uncertain significance |
| rs1137933 | 17:26,105,932 | G/A | synonymous variant | benign |
| rs200391593 | 17:26,105,952 | C/T | — | uncertain significance |
| rs140983392 | 17:26,106,007 | G/A | — | likely benign |
| rs2545029573 | 17:26,106,022 | C/G | — | uncertain significance |
| rs201238156 | 17:26,106,069 | G/A | — | uncertain significance |
| rs202005766 | 17:26,106,081 | A/G | — | uncertain significance |
| rs189687047 | 17:26,106,092 | A/G | — | benign |
| rs186255750 | 17:26,106,192 | G/A | intron variant | — |
| rs4795067 | 17:26,106,675 | A/G | intron variant | — |
| rs34719207 | 17:26,107,840 | G/A | — | benign |
| rs747955388 | 17:26,107,907 | G/A | — | uncertain significance |
Showing 100 of 140 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.