PLIN4
perilipin 4
Summary
Members of the perilipin family, such as PLIN4, coat intracellular lipid storage droplets (Wolins et al., 2003 [PubMed 12840023]).[supplied by OMIM, Feb 2010]
Known Variants168 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs528022375 | 19:4,502,785 | C/T | — | — |
| rs182777366 | 19:4,504,480 | G/A | — | likely benign |
| rs567719914 | 19:4,504,559 | C/G | — | uncertain significance |
| rs1159663200 | 19:4,504,581 | C/T | — | uncertain significance |
| rs780402327 | 19:4,504,589 | C/T | — | uncertain significance |
| rs200236765 | 19:4,504,620 | C/T | — | uncertain significance |
| rs766941356 | 19:4,504,652 | A/T | — | uncertain significance |
| rs781064414 | 19:4,504,655 | T/G | — | uncertain significance |
| rs1976032459 | 19:4,504,668 | G/A | — | uncertain significance |
| rs567197961 | 19:4,504,670 | C/T | — | uncertain significance |
| rs2512464942 | 19:4,504,674 | C/T | — | uncertain significance |
| rs761289278 | 19:4,504,677 | G/A | — | uncertain significance |
| rs202096657 | 19:4,504,701 | C/G | — | uncertain significance |
| rs778167684 | 19:4,504,709 | C/T | — | uncertain significance |
| rs2512465317 | 19:4,504,737 | A/C | — | uncertain significance |
| rs762524648 | 19:4,504,755 | G/A | — | uncertain significance |
| rs374440413 | 19:4,504,758 | G/A | — | uncertain significance |
| rs371909957 | 19:4,504,895 | G/A | — | likely benign |
| rs755865538 | 19:4,504,956 | C/T | — | uncertain significance |
| rs11879706 | 19:4,505,356 | C/G | — | — |
| rs749993229 | 19:4,508,835 | T/G | — | uncertain significance |
| rs748446959 | 19:4,508,853 | G/A | — | uncertain significance |
| rs770941980 | 19:4,508,859 | T/C | — | uncertain significance |
| rs368533613 | 19:4,508,868 | C/T | — | uncertain significance |
| rs779022748 | 19:4,508,919 | T/C | — | uncertain significance |
| rs368569854 | 19:4,508,928 | G/A | — | uncertain significance |
| rs374955660 | 19:4,508,932 | G/C | — | uncertain significance |
| rs371310725 | 19:4,508,944 | C/T | — | uncertain significance |
| rs60328144 | 19:4,509,469 | A/G | — | — |
| rs200482765 | 19:4,510,079 | A/T | — | — |
| rs2512123789 | 19:4,510,479 | G/T | — | uncertain significance |
| rs539590372 | 19:4,510,494 | C/T | — | uncertain significance |
| rs199694958 | 19:4,510,529 | C/T | — | uncertain significance |
| rs761518216 | 19:4,510,542 | C/T | — | uncertain significance |
| rs769420900 | 19:4,510,543 | G/A | — | likely benign |
| rs371086662 | 19:4,510,584 | C/T | — | uncertain significance |
| rs1329067440 | 19:4,510,709 | G/A | — | likely benign |
| rs1176234741 | 19:4,510,725 | T/C | — | uncertain significance |
| rs750031731 | 19:4,510,765 | A/T | — | uncertain significance |
| rs1328177809 | 19:4,510,776 | C/T | — | uncertain significance |
| rs781509044 | 19:4,510,791 | C/T | — | uncertain significance |
| rs144380069 | 19:4,510,792 | G/A | — | likely benign |
| rs2512126031 | 19:4,510,800 | T/C | — | likely benign |
| rs369001887 | 19:4,510,849 | C/T | — | likely benign |
| rs200831658 | 19:4,510,855 | G/C | — | uncertain significance |
| rs1381994037 | 19:4,510,883 | A/G | — | likely benign |
| rs558202117 | 19:4,510,886 | G/T | — | uncertain significance |
| rs370647633 | 19:4,510,899 | C/T | — | uncertain significance |
| rs773231775 | 19:4,510,944 | C/A | — | uncertain significance |
| rs2512127270 | 19:4,510,964 | C/T | — | uncertain significance |
| rs1976288975 | 19:4,510,968 | T/A | — | uncertain significance |
| rs745942098 | 19:4,510,971 | C/T | — | uncertain significance |
| rs369383954 | 19:4,511,037 | C/T | — | likely benign |
| rs762943924 | 19:4,511,136 | C/T | — | likely benign |
| rs150943101 | 19:4,511,157 | C/T | — | uncertain significance |
| rs199625614 | 19:4,511,197 | G/A | — | likely benign |
| rs200718202 | 19:4,511,200 | C/T | — | likely benign |
| rs752898669 | 19:4,511,202 | G/A | — | likely benign |
| rs746541245 | 19:4,511,216 | G/T | — | uncertain significance |
| rs750260863 | 19:4,511,250 | A/C | — | likely benign |
| rs1238826012 | 19:4,511,300 | A/G | — | uncertain significance |
| rs758629481 | 19:4,511,354 | G/A | — | likely benign |
| rs200538852 | 19:4,511,400 | C/T | — | uncertain significance |
| rs759846421 | 19:4,511,409 | G/T | — | likely benign |
| rs777879018 | 19:4,511,416 | T/G | — | uncertain significance |
| rs1034700124 | 19:4,511,478 | C/T | — | uncertain significance |
| rs750505528 | 19:4,511,483 | T/C | — | uncertain significance |
| rs544718313 | 19:4,511,513 | G/A | — | uncertain significance |
| rs372120790 | 19:4,511,571 | T/G | — | uncertain significance |
| rs201218860 | 19:4,511,612 | G/T | — | uncertain significance |
| rs768830418 | 19:4,511,613 | T/G | — | uncertain significance |
| rs762684785 | 19:4,511,617 | C/T | — | uncertain significance |
| rs763801844 | 19:4,511,628 | G/T | — | uncertain significance |
| rs2512133419 | 19:4,511,630 | A/G | — | uncertain significance |
| rs2512133492 | 19:4,511,636 | C/T | — | uncertain significance |
| rs2512133512 | 19:4,511,637 | C/T | — | uncertain significance |
| rs746419226 | 19:4,511,642 | G/A | — | uncertain significance |
| rs2512133570 | 19:4,511,643 | C/T | — | uncertain significance |
| rs775085816 | 19:4,511,674 | C/T | — | likely benign |
| rs759223445 | 19:4,511,680 | A/G | — | likely benign |
| rs2512133937 | 19:4,511,694 | T/C | — | uncertain significance |
| rs1255308929 | 19:4,511,713 | G/C | — | uncertain significance |
| rs778005554 | 19:4,511,720 | C/T | — | uncertain significance |
| rs545793182 | 19:4,511,721 | C/T | — | uncertain significance |
| rs62115190 | 19:4,511,730 | T/C | — | benign |
| rs201336186 | 19:4,511,789 | C/T | — | likely benign |
| rs547568062 | 19:4,511,841 | C/T | — | uncertain significance |
| rs779510597 | 19:4,511,898 | C/T | — | uncertain significance |
| rs375758336 | 19:4,511,909 | G/T | — | uncertain significance |
| rs771198537 | 19:4,511,912 | T/C | — | uncertain significance |
| rs1439818345 | 19:4,511,915 | A/G | — | uncertain significance |
| rs763855887 | 19:4,511,918 | C/A | — | uncertain significance |
| rs776376884 | 19:4,511,919 | C/T | — | uncertain significance |
| rs113818201 | 19:4,511,928 | C/A | — | conflicting classifications of pathogenicity |
| rs1976389969 | 19:4,511,988 | C/G | — | uncertain significance |
| rs111370954 | 19:4,511,992 | C/T | — | likely benign |
| rs200977488 | 19:4,512,008 | G/A | — | uncertain significance |
| rs267605474 | 19:4,512,018 | C/A | — | uncertain significance |
| rs375606798 | 19:4,512,020 | G/A | — | uncertain significance |
| rs201957398 | 19:4,512,048 | C/T | — | likely benign |
Showing 100 of 168 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.