HS3ST6
heparan sulfate-glucosamine 3-sulfotransferase 6
Summary
Predicted to enable [heparan sulfate]-glucosamine 3-sulfotransferase activity. Predicted to be involved in heparan sulfate proteoglycan biosynthetic process. Predicted to act upstream of or within blastocyst hatching. Predicted to be located in Golgi membrane. Implicated in hereditary angioedema. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs337285 | 16:1,961,674 | C/G | — | uncertain significance |
| rs1355674585 | 16:1,961,677 | C/A | — | uncertain significance |
| rs760978161 | 16:1,961,688 | C/T | — | uncertain significance |
| rs372823212 | 16:1,961,724 | C/T | — | uncertain significance |
| rs2548220158 | 16:1,961,751 | T/C | — | uncertain significance |
| rs1418131078 | 16:1,961,758 | A/G | — | uncertain significance |
| rs556124596 | 16:1,961,776 | C/T | — | uncertain significance |
| rs199919782 | 16:1,961,852 | C/T | — | likely benign |
| rs77148094 | 16:1,961,863 | C/T | — | uncertain significance |
| rs200057891 | 16:1,961,868 | C/T | — | uncertain significance |
| rs368226042 | 16:1,961,869 | G/A | — | uncertain significance |
| rs2548220535 | 16:1,961,870 | C/A | — | uncertain significance |
| rs922758380 | 16:1,961,922 | T/G | — | uncertain significance |
| rs373858942 | 16:1,961,953 | C/T | — | uncertain significance |
| rs762751833 | 16:1,962,003 | G/T | — | uncertain significance |
| rs199988789 | 16:1,962,004 | C/T | — | uncertain significance |
| rs201954014 | 16:1,962,007 | G/A | — | uncertain significance |
| rs780923344 | 16:1,962,036 | A/G | — | uncertain significance |
| rs761161730 | 16:1,962,052 | C/T | — | uncertain significance |
| rs199582508 | 16:1,962,104 | C/T | — | likely benign |
| rs569242276 | 16:1,962,111 | A/G | — | uncertain significance |
| rs202049960 | 16:1,962,123 | C/T | — | uncertain significance |
| rs373745703 | 16:1,962,124 | G/A | — | uncertain significance |
| rs367587631 | 16:1,962,126 | C/T | — | uncertain significance |
| rs764581907 | 16:1,962,134 | C/A | — | uncertain significance |
| rs746467957 | 16:1,962,190 | T/A | — | pathogenic |
| rs201534989 | 16:1,967,915 | T/A | — | uncertain significance |
| rs202178909 | 16:1,967,918 | C/A | — | uncertain significance |
| rs1376604338 | 16:1,968,062 | C/T | — | uncertain significance |
| rs771232072 | 16:1,968,071 | G/T | — | uncertain significance |
| rs775482169 | 16:1,968,095 | G/C | — | uncertain significance |
| rs1567300028 | 16:1,968,116 | G/C | — | uncertain significance |
| rs2548224861 | 16:1,968,144 | C/T | — | uncertain significance |
| rs1432816996 | 16:1,968,210 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.