RBM6
RNA binding motif protein 6
Summary
Enables RNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants86 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7635002 | 3:49,989,155 | T/G | intron variant | — |
| rs11130226 | 3:49,993,191 | T/A | — | — |
| rs12636669 | 3:50,003,323 | C/T | intron variant | — |
| rs2352969 | 3:50,003,632 | G/C | intron variant | — |
| rs368376344 | 3:50,005,081 | T/C | — | uncertain significance |
| rs138262796 | 3:50,005,082 | A/G | — | uncertain significance |
| rs775742397 | 3:50,005,096 | G/A | — | uncertain significance |
| rs374876120 | 3:50,005,100 | C/T | — | uncertain significance |
| rs202185790 | 3:50,005,146 | G/C | — | uncertain significance |
| rs368052154 | 3:50,005,151 | G/C | — | uncertain significance |
| rs777118077 | 3:50,005,160 | C/T | — | uncertain significance |
| rs147134668 | 3:50,005,331 | G/A | — | uncertain significance |
| rs147790577 | 3:50,005,339 | C/T | — | uncertain significance |
| rs2545515496 | 3:50,005,353 | C/G | — | uncertain significance |
| rs775469883 | 3:50,005,391 | G/A | — | uncertain significance |
| rs201237350 | 3:50,005,463 | A/G | — | uncertain significance |
| rs958730517 | 3:50,005,480 | A/G | — | uncertain significance |
| rs1249861526 | 3:50,005,493 | G/A | — | uncertain significance |
| rs138846313 | 3:50,005,513 | G/C | — | uncertain significance |
| rs2084591506 | 3:50,005,560 | C/G | — | uncertain significance |
| rs369268393 | 3:50,005,613 | C/T | — | uncertain significance |
| rs1269876401 | 3:50,005,637 | G/C | — | uncertain significance |
| rs529537939 | 3:50,005,657 | C/G | — | uncertain significance |
| rs199587862 | 3:50,005,680 | G/A | — | uncertain significance |
| rs552334748 | 3:50,005,717 | C/T | — | likely benign |
| rs1028110367 | 3:50,005,820 | C/T | — | uncertain significance |
| rs2084611645 | 3:50,005,887 | A/C | — | uncertain significance |
| rs766781283 | 3:50,005,981 | C/T | — | uncertain significance |
| rs200325933 | 3:50,005,991 | A/G | — | uncertain significance |
| rs148635727 | 3:50,006,026 | G/A | — | benign |
| rs768216335 | 3:50,006,039 | T/A | — | uncertain significance |
| rs771389774 | 3:50,006,045 | G/A | — | uncertain significance |
| rs746347509 | 3:50,006,126 | A/G | — | uncertain significance |
| rs775685235 | 3:50,006,144 | A/G | — | uncertain significance |
| rs750436785 | 3:50,006,171 | G/A | — | uncertain significance |
| rs777371769 | 3:50,009,561 | G/A | — | uncertain significance |
| rs11130229 | 3:50,011,540 | T/C | intron variant | — |
| rs2545545827 | 3:50,012,774 | A/G | — | uncertain significance |
| rs11916261 | 3:50,014,496 | G/A | intron variant | — |
| rs62262139 | 3:50,022,049 | G/C | — | — |
| rs62262140 | 3:50,022,054 | G/A | — | — |
| rs139738301 | 3:50,022,064 | G/A | — | — |
| rs377609499 | 3:50,022,069 | G/A | — | — |
| rs149445151 | 3:50,022,079 | G/A | — | — |
| rs199956414 | 3:50,022,089 | G/A | — | — |
| rs111439884 | 3:50,024,038 | A/T | — | — |
| rs146958887 | 3:50,025,158 | G/A | intron variant | — |
| rs11925088 | 3:50,029,386 | T/G | intron variant | — |
| rs35012435 | 3:50,031,840 | C/G | — | — |
| rs571930760 | 3:50,035,015 | T/C | — | — |
| rs11925192 | 3:50,038,664 | G/A | intron variant | — |
| rs7634917 | 3:50,049,299 | T/G | intron variant | — |
| rs6800913 | 3:50,052,867 | T/C | — | — |
| rs6800916 | 3:50,052,873 | T/A | intron variant | — |
| rs2624818 | 3:50,056,265 | G/T | — | — |
| rs35849525 | 3:50,067,350 | T/C | intron variant | — |
| rs138014720 | 3:50,070,843 | A/T | intron variant | — |
| rs143050036 | 3:50,071,965 | C/A | — | — |
| rs66851636 | 3:50,073,046 | C/T | intron variant | — |
| rs112634398 | 3:50,075,494 | A/G | intron variant | — |
| rs12631248 | 3:50,080,174 | C/G | intron variant | — |
| rs148920216 | 3:50,085,708 | A/G | — | uncertain significance |
| rs540281247 | 3:50,086,305 | C/T | — | — |
| rs62263580 | 3:50,087,725 | G/A | regulatory region variant | — |
| rs6762477 | 3:50,093,209 | G/A | intron variant | — |
| rs147018443 | 3:50,095,213 | C/T | — | likely benign |
| rs754544321 | 3:50,095,429 | G/C | — | uncertain significance |
| rs779354599 | 3:50,095,850 | G/A | — | uncertain significance |
| rs2089858799 | 3:50,097,092 | G/A | — | uncertain significance |
| rs34707170 | 3:50,097,113 | A/G | — | benign |
| rs190912901 | 3:50,097,958 | A/G | intron variant | — |
| rs759986993 | 3:50,098,424 | A/C | — | uncertain significance |
| rs772615456 | 3:50,098,640 | G/T | — | uncertain significance |
| rs2545871582 | 3:50,098,922 | C/G | — | uncertain significance |
| rs1475008267 | 3:50,098,951 | G/T | — | uncertain significance |
| rs2089960907 | 3:50,099,447 | A/C | — | uncertain significance |
| rs6793528 | 3:50,100,188 | C/T | — | — |
| rs765899020 | 3:50,102,480 | G/C | — | uncertain significance |
| rs147895205 | 3:50,103,758 | G/A | — | benign |
| rs1417066514 | 3:50,103,778 | G/A | — | uncertain significance |
| rs747519611 | 3:50,103,789 | C/T | — | uncertain significance |
| rs370878069 | 3:50,112,639 | G/A | — | uncertain significance |
| rs755798395 | 3:50,112,659 | G/C | — | uncertain significance |
| rs199633632 | 3:50,112,663 | T/C | — | likely benign |
| rs1454210341 | 3:50,112,719 | A/G | — | likely benign |
| rs562534362 | 3:50,112,732 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.