YLPM1
YLP motif containing 1
Summary
Enables RNA binding activity. Predicted to be involved in regulation of telomere maintenance. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Located in nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants159 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778679863 | 14:75,230,215 | A/G | — | uncertain significance |
| rs2503389580 | 14:75,230,244 | C/T | — | uncertain significance |
| rs1424486451 | 14:75,230,245 | C/G | — | uncertain significance |
| rs2090870900 | 14:75,230,248 | T/C | — | uncertain significance |
| rs2503389952 | 14:75,230,302 | C/G | — | uncertain significance |
| rs1036345996 | 14:75,230,433 | C/T | — | uncertain significance |
| rs780141684 | 14:75,230,457 | C/T | — | uncertain significance |
| rs2503391015 | 14:75,230,473 | G/A | — | uncertain significance |
| rs368367178 | 14:75,230,571 | A/C | — | uncertain significance |
| rs2503391727 | 14:75,230,586 | C/G | — | uncertain significance |
| rs763896644 | 14:75,230,591 | C/G | — | uncertain significance |
| rs372131920 | 14:75,230,613 | A/G | — | uncertain significance |
| rs755193062 | 14:75,230,631 | C/G | — | uncertain significance |
| rs779112462 | 14:75,230,632 | C/G | — | uncertain significance |
| rs139231018 | 14:75,230,654 | T/A | — | benign |
| rs199939020 | 14:75,230,662 | A/G | — | uncertain significance |
| rs369288881 | 14:75,230,666 | G/A | — | uncertain significance |
| rs765397089 | 14:75,230,685 | A/C | — | uncertain significance |
| rs758686163 | 14:75,230,688 | C/G | — | uncertain significance |
| rs751717978 | 14:75,230,689 | C/T | — | uncertain significance |
| rs2090881135 | 14:75,230,709 | T/G | — | uncertain significance |
| rs2503392855 | 14:75,230,730 | T/C | — | uncertain significance |
| rs2090882809 | 14:75,230,773 | C/T | — | uncertain significance |
| rs2503393208 | 14:75,230,779 | C/T | — | uncertain significance |
| rs1204052604 | 14:75,230,809 | C/G | — | uncertain significance |
| rs376901037 | 14:75,230,890 | C/T | — | uncertain significance |
| rs2503394156 | 14:75,230,923 | T/G | — | uncertain significance |
| rs370181759 | 14:75,230,952 | C/G | — | uncertain significance |
| rs377086069 | 14:75,230,967 | A/G | — | uncertain significance |
| rs374055401 | 14:75,230,993 | T/C | — | likely benign |
| rs34752362 | 14:75,232,306 | G/A | intron variant | — |
| rs2193596 | 14:75,234,101 | T/C | — | — |
| rs142846161 | 14:75,245,215 | G/A | — | likely benign |
| rs376895690 | 14:75,245,225 | A/G | — | uncertain significance |
| rs1263164676 | 14:75,245,247 | A/T | — | uncertain significance |
| rs376584536 | 14:75,245,312 | C/T | — | uncertain significance |
| rs1381997291 | 14:75,245,370 | C/T | — | uncertain significance |
| rs376066218 | 14:75,247,192 | G/A | — | uncertain significance |
| rs2503437875 | 14:75,247,226 | C/G | — | uncertain significance |
| rs953644647 | 14:75,247,247 | A/G | — | uncertain significance |
| rs1309278238 | 14:75,247,283 | T/C | — | uncertain significance |
| rs7154845 | 14:75,247,746 | A/G | intron variant | — |
| rs2503440478 | 14:75,248,085 | C/A | — | uncertain significance |
| rs138920894 | 14:75,248,101 | A/T | — | benign |
| rs752665257 | 14:75,248,107 | A/C | — | uncertain significance |
| rs763122373 | 14:75,248,259 | A/G | — | uncertain significance |
| rs1459720650 | 14:75,248,260 | A/G | — | uncertain significance |
| rs2091092602 | 14:75,248,290 | C/T | — | uncertain significance |
| rs375571082 | 14:75,248,292 | A/G | — | uncertain significance |
| rs367613144 | 14:75,248,301 | C/T | — | uncertain significance |
| rs1243467259 | 14:75,248,320 | A/G | — | uncertain significance |
| rs769597353 | 14:75,248,343 | A/G | — | uncertain significance |
| rs201292705 | 14:75,248,388 | C/T | — | uncertain significance |
| rs375413526 | 14:75,248,433 | C/T | — | uncertain significance |
| rs1184404294 | 14:75,248,436 | G/C | — | uncertain significance |
| rs749041517 | 14:75,248,487 | T/C | — | uncertain significance |
| rs2091096967 | 14:75,248,512 | C/T | — | uncertain significance |
| rs766804031 | 14:75,248,520 | C/T | — | uncertain significance |
| rs755024480 | 14:75,248,634 | C/T | — | uncertain significance |
| rs2287401 | 14:75,248,669 | G/T | — | benign |
| rs1047917801 | 14:75,248,672 | A/G | — | uncertain significance |
| rs773929601 | 14:75,248,677 | C/T | — | uncertain significance |
| rs371270075 | 14:75,248,695 | C/T | — | uncertain significance |
| rs528287760 | 14:75,248,707 | C/T | — | uncertain significance |
| rs904304852 | 14:75,248,772 | T/C | — | uncertain significance |
| rs367692362 | 14:75,248,791 | C/T | — | uncertain significance |
| rs370377125 | 14:75,248,796 | A/G | — | uncertain significance |
| rs201815018 | 14:75,248,803 | A/G | — | uncertain significance |
| rs1446300494 | 14:75,248,806 | C/G | — | uncertain significance |
| rs776457842 | 14:75,248,835 | C/A | — | uncertain significance |
| rs1046649223 | 14:75,248,901 | G/C | — | uncertain significance |
| rs2503445209 | 14:75,248,935 | C/A | — | uncertain significance |
| rs1223085574 | 14:75,248,951 | G/T | — | uncertain significance |
| rs2503445368 | 14:75,248,970 | G/A | — | uncertain significance |
| rs34956813 | 14:75,254,167 | G/A | intron variant | — |
| rs35809608 | 14:75,254,762 | A/G | intron variant | — |
| rs35769520 | 14:75,255,115 | G/A | intron variant | — |
| rs1451310221 | 14:75,264,288 | A/T | — | uncertain significance |
| rs567074692 | 14:75,264,350 | C/T | — | uncertain significance |
| rs1566750894 | 14:75,264,369 | C/T | — | uncertain significance |
| rs201043835 | 14:75,264,404 | G/A | — | likely benign |
| rs2503478122 | 14:75,264,537 | A/G | — | uncertain significance |
| rs776350956 | 14:75,264,575 | C/T | — | uncertain significance |
| rs764652921 | 14:75,264,617 | C/G | — | uncertain significance |
| rs754592650 | 14:75,264,645 | C/G | — | uncertain significance |
| rs2091280506 | 14:75,264,656 | A/G | — | uncertain significance |
| rs2503478640 | 14:75,264,669 | T/C | — | uncertain significance |
| rs757874376 | 14:75,264,674 | G/T | — | uncertain significance |
| rs368741456 | 14:75,264,767 | A/C | — | uncertain significance |
| rs2503479474 | 14:75,264,839 | C/T | — | uncertain significance |
| rs369432574 | 14:75,264,849 | A/T | — | uncertain significance |
| rs766713884 | 14:75,264,851 | C/T | — | uncertain significance |
| rs1341751636 | 14:75,264,933 | C/T | — | uncertain significance |
| rs779035292 | 14:75,264,957 | G/C | — | uncertain significance |
| rs2503480165 | 14:75,264,971 | C/T | — | uncertain significance |
| rs376183084 | 14:75,264,992 | A/G | — | uncertain significance |
| rs1164379651 | 14:75,265,005 | G/A | — | uncertain significance |
| rs1251367389 | 14:75,265,019 | G/A | — | uncertain significance |
| rs768261571 | 14:75,265,020 | A/G | — | uncertain significance |
| rs766663389 | 14:75,265,094 | C/T | — | uncertain significance |
Showing 100 of 159 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.