PSORS1C1
psoriasis susceptibility 1 candidate 1
Summary
This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1265044 | 6:31,090,318 | C/T | upstream gene variant | — |
| rs3130998 | 6:31,090,945 | C/G | — | — |
| rs3130999 | 6:31,091,197 | A/G | upstream gene variant | — |
| rs3778630 | 6:31,091,328 | G/A | upstream gene variant | — |
| rs9263688 | 6:31,091,967 | A/G | upstream gene variant | — |
| rs3094204 | 6:31,091,992 | A/G | upstream gene variant | — |
| rs3095307 | 6:31,092,049 | G/C | upstream gene variant | — |
| rs3094200 | 6:31,093,132 | A/G | regulatory region variant | — |
| rs3815087 | 6:31,093,587 | G/A | regulatory region variant | — |
| rs112588188 | 6:31,094,069 | G/A | regulatory region variant | — |
| rs3130556 | 6:31,094,636 | C/T | intron variant | — |
| rs9263715 | 6:31,095,801 | G/T | — | — |
| rs3130559 | 6:31,097,301 | C/T | intron variant | — |
| rs374244467 | 6:31,097,432 | C/G | — | likely benign |
| rs13196568 | 6:31,098,400 | G/A | — | — |
| rs4959053 | 6:31,099,577 | G/A | intron variant | — |
| rs3130561 | 6:31,100,768 | T/C | downstream gene variant | — |
| rs3823417 | 6:31,100,869 | G/C | — | — |
| rs3823418 | 6:31,100,942 | G/A | downstream gene variant | — |
| rs3130562 | 6:31,100,974 | T/C | downstream gene variant | — |
| rs3823419 | 6:31,101,001 | G/A | downstream gene variant | — |
| rs3130563 | 6:31,101,250 | T/C | downstream gene variant | — |
| rs4084091 | 6:31,101,401 | C/T | downstream gene variant | — |
| rs3132569 | 6:31,101,426 | G/T | — | — |
| rs3130565 | 6:31,101,778 | T/C | downstream gene variant | — |
| rs9468873 | 6:31,101,880 | T/C | downstream gene variant | — |
| rs10947140 | 6:31,102,143 | G/C | — | — |
| rs75881311 | 6:31,102,273 | T/A | downstream gene variant | — |
| rs3130566 | 6:31,102,618 | C/T | — | — |
| rs3132565 | 6:31,102,964 | A/T | — | — |
| rs3094669 | 6:31,103,195 | C/G | downstream gene variant | — |
| rs1265101 | 6:31,104,061 | G/A | downstream gene variant | — |
| rs558745444 | 6:31,104,693 | C/T | — | — |
| rs3094665 | 6:31,104,855 | G/C | downstream gene variant | — |
| rs9263724 | 6:31,104,956 | G/C | — | — |
| rs74762922 | 6:31,105,011 | A/G | downstream gene variant | — |
| rs3131010 | 6:31,105,147 | C/T | downstream gene variant | — |
| rs3130573 | 6:31,106,268 | A/G | downstream gene variant | — |
| rs73397071 | 6:31,106,423 | T/C | — | benign |
| rs1265097 | 6:31,106,459 | A/C | — | benign |
| rs1265096 | 6:31,106,489 | G/A | — | benign |
| rs540640358 | 6:31,106,498 | C/T | — | uncertain significance |
| rs9263726 | 6:31,106,499 | G/A | missense variant | benign |
| rs9501057 | 6:31,106,516 | C/T | — | benign |
| rs111892391 | 6:31,106,523 | G/T | — | likely benign |
| rs1265093 | 6:31,107,187 | G/A | downstream gene variant | — |
| rs2285803 | 6:31,107,258 | T/C | downstream gene variant | — |
| rs2233945 | 6:31,107,361 | C/A | downstream gene variant | — |
| rs2233944 | 6:31,107,422 | G/T | — | benign |
| rs2233943 | 6:31,107,447 | C/G | — | benign |
| rs1051311395 | 6:31,107,486 | G/C | — | uncertain significance |
| rs1211942992 | 6:31,107,594 | A/G | — | uncertain significance |
| rs1063646 | 6:31,107,648 | C/T | — | benign |
| rs992398829 | 6:31,107,686 | T/A | — | uncertain significance |
| rs1265091 | 6:31,108,129 | C/T | downstream gene variant | — |
| rs7771067 | 6:31,108,306 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.