FAM178B
family with sequence similarity 178 member B
Known Variants20 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs552281954 | 2:97,543,683 | G/T | — | uncertain significance |
| rs1466604345 | 2:97,543,700 | C/T | — | likely benign |
| rs371471695 | 2:97,543,725 | G/A | — | uncertain significance |
| rs200958044 | 2:97,544,199 | A/C | — | uncertain significance |
| rs776809751 | 2:97,544,229 | G/A | — | likely benign |
| rs747403258 | 2:97,559,745 | G/C | — | uncertain significance |
| rs369630987 | 2:97,559,773 | G/A | — | uncertain significance |
| rs774250251 | 2:97,559,781 | G/A | — | likely benign |
| rs2314650 | 2:97,564,284 | G/A | intron variant | — |
| rs6728642 | 2:97,607,071 | A/G | intron variant | — |
| rs190784220 | 2:97,624,149 | G/T | upstream gene variant | — |
| rs757675684 | 2:97,636,502 | C/A | — | uncertain significance |
| rs559244924 | 2:97,637,714 | G/C | — | uncertain significance |
| rs2153375779 | 2:97,637,789 | A/C | — | uncertain significance |
| rs2467048828 | 2:97,637,792 | A/C | — | uncertain significance |
| rs2467048836 | 2:97,637,798 | A/C | — | uncertain significance |
| rs1007881524 | 2:97,637,870 | C/T | — | uncertain significance |
| rs544078503 | 2:97,637,886 | A/G | — | uncertain significance |
| rs890539276 | 2:97,638,039 | C/T | — | likely benign |
| rs775075494 | 2:97,638,292 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.