FAM53B
family with sequence similarity 53 member B
Summary
Involved in positive regulation of canonical Wnt signaling pathway. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs769051630 | 10:126,311,848 | T/A | — | uncertain significance |
| rs760767354 | 10:126,311,876 | C/A | — | uncertain significance |
| rs148677670 | 10:126,311,881 | C/T | — | uncertain significance |
| rs745387817 | 10:126,311,888 | G/A | — | uncertain significance |
| rs373224205 | 10:126,311,893 | G/C | — | uncertain significance |
| rs976202424 | 10:126,312,068 | C/T | — | uncertain significance |
| rs753417235 | 10:126,312,107 | G/C | — | uncertain significance |
| rs781622801 | 10:126,312,170 | A/G | — | uncertain significance |
| rs897297 | 10:126,319,487 | A/G | intron variant | — |
| rs12571573 | 10:126,323,011 | G/A | intron variant | — |
| rs10901793 | 10:126,324,209 | G/A | intron variant | — |
| rs78708879 | 10:126,334,723 | G/A | regulatory region variant | — |
| rs139984976 | 10:126,351,017 | A/C | intron variant | — |
| rs34410705 | 10:126,352,680 | C/T | intron variant | — |
| rs10901802 | 10:126,354,554 | G/T | — | — |
| rs4962681 | 10:126,359,575 | G/A | intron variant | — |
| rs7093768 | 10:126,370,067 | C/T | intron variant | — |
| rs779220632 | 10:126,370,307 | G/A | — | uncertain significance |
| rs572365285 | 10:126,370,312 | G/A | — | uncertain significance |
| rs2495552882 | 10:126,370,376 | A/C | — | uncertain significance |
| rs754765742 | 10:126,370,410 | G/C | — | uncertain significance |
| rs141630750 | 10:126,370,430 | C/T | — | likely benign |
| rs370552494 | 10:126,370,516 | C/A | — | uncertain significance |
| rs748353565 | 10:126,370,622 | G/A | — | uncertain significance |
| rs775274264 | 10:126,370,636 | C/A | — | uncertain significance |
| rs763763733 | 10:126,370,648 | C/T | — | uncertain significance |
| rs1429776106 | 10:126,370,673 | C/T | — | uncertain significance |
| rs953554433 | 10:126,370,739 | G/A | — | uncertain significance |
| rs367682100 | 10:126,370,820 | C/T | — | uncertain significance |
| rs372875771 | 10:126,370,838 | C/T | — | uncertain significance |
| rs1044885132 | 10:126,370,915 | C/G | — | uncertain significance |
| rs2885521 | 10:126,373,313 | C/T | intron variant | — |
| rs11245331 | 10:126,382,353 | G/A | regulatory region variant | — |
| rs552700585 | 10:126,383,059 | T/A | — | — |
| rs10901807 | 10:126,384,610 | G/A | intron variant | — |
| rs3781449 | 10:126,390,424 | T/G | — | — |
| rs760911476 | 10:126,395,248 | C/T | — | likely benign |
| rs766552006 | 10:126,395,249 | G/A | — | uncertain significance |
| rs2272005 | 10:126,402,100 | C/T | coding sequence variant | — |
| rs10794177 | 10:126,407,409 | G/C | downstream gene variant | — |
| rs7097890 | 10:126,411,015 | T/C | intron variant | — |
| rs11245343 | 10:126,415,795 | T/C | intron variant | — |
| rs11245344 | 10:126,418,782 | C/T | intron variant | — |
| rs4962691 | 10:126,424,137 | C/T | intron variant | — |
| rs2629540 | 10:126,426,148 | G/C | intron variant | — |
| rs10901813 | 10:126,429,875 | G/A | regulatory region variant | — |
| rs34884690 | 10:126,431,711 | G/A | intron variant | — |
| rs3824765 | 10:126,433,570 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.