| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs375156789 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994608 | AATCTGGAGACTTGC[A/G]GTGGTGGCGGTGGTG | 9051 |
| rs375161786 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006911 | CTTCTTTTTCAAGAT[G/T]GTTTTGGCTCTTTGG | 9051 |
| rs375253913 | in-del | -/GCATCTGCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034831 | TCTGCCGCATCTGCC[-/GCATCTGCC]TCTTCTGTTTTATTT | 9051 |
| rs375294517 | snp | A/G | 5.54995e-05 | 0.00526751 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030505 | CTGCGCTTTCAGAGC[A/G]GGTATACAGGCAGAG | 9051 |
| rs375295026 | snp | A/G | 0.000165986 | 0.00910855 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018544 | CAAGTAAGATCTCCC[A/G]GGCCCTGGGGCTCAC | 9051 |
| rs375299192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999319 | AATCTTACTCTGTCA[C/T]CCAGGCTGGAGGGCA | 9051 |
| rs375469954 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015250 | TTCCTGGGCTGTCTA[C/T]TAAATGGCTGATGTA | 9051 |
| rs375519270 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995184 | CCTGGCCCGGCCCGA[A/G]CTCCAGCCTGCCTCT | 9051 |
| rs375721426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020709 | TAGGGCCCATTTATG[C/T]GCCACCTCCTCCAGG | 9051 |
| rs375865116 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013414 | GTCTCCATGGGGGGG[G/T]GGTGGGGCACAGGCC | 9051 |
| rs375873529 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024857 | GCCACCTGCTGAGAG[A/C]CCATCTGAACACTGT | 9051 |
| rs375877680 | snp | A/G | 3.33751e-05 | 0.0040849 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995559 | AGTGAGCTTTGCCGC[A/G]GCAGACGCCTGAGGA | 9051 |
| rs375904710 | in-del | -/GGTG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020879 | CCTGTGGGGGGGGGG[-/GGTG]TGTGTGTTGGCCCTC | 9051 |
| rs375910918 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030247 | AGAGATGCCCAGAGG[C/G]CAATACTCTGGACTT | 9051 |
| rs375932577 | snp | C/G | 7.51767e-05 | 0.00613047 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028590 | AAGTGCCGGGACGCG[C/G]ACGACGCGGAGCAGG | 9051 |
| rs375950478 | snp | A/G | 0.00662519 | 0.0571725 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77029555 | AGCCAGGCAGTGCAA[A/G]GACTCGGCCACCGAG | 9051 |
| rs376017101 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033504 | TGAGTGACGAAGGTG[A/G]CAGCCCATTGGGAGC | 9051 |
| rs376034586 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996516 | GACGCTCTGGCCCTC[A/G]GCTCAGCCGGCTGAG | 9051 |
| rs376044745 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015275 | ATGTAGGTATATGGC[-/T]TTTGGGGACAGGTTG | 9051 |
| rs376097505 | snp | A/G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000181 | GACAGCACCGCTGCC[A/G/T]AGTGGGGCAGTGACT | 9051 |
| rs376128040 | snp | G/T | 0.000302641 | 0.0122975 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018148 | TGTCCTGTGTCACAG[G/T]GCAGGGACTTCACAG | 9051 |
| rs376276381 | snp | C/T | 0.00121203 | 0.0245875 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037197 | GGCCAGGAGCCCCTT[C/T]GGACCTGCCCTGCCA | 9051 |
| rs376289639 | snp | C/T | 4.96339e-05 | 0.00498142 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025467 | CCATCAGATCTGACA[C/T]TGGGGACCAGTATCC | 9051 |
| rs376437386 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010058 | TCCTCCAGGGCTTGG[A/G]GTCTGGGGTGGCTCA | 9051 |
| rs376465836 | snp | A/G | 1.68516e-05 | 0.00290268 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037023 | CCCTTCCAACGTCAT[A/G]CGCTTTCAATCTCTT | 9051 |
| rs376484540 | snp | C/T | 0.000333695 | 0.0129126 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029595 | TGGGCCTGGCTGCCC[C/T]GTCCGACCAGGGCGG | 9051 |
| rs376565378 | snp | C/T | 3.32934e-05 | 0.0040799 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025332 | GCGTAAGTCCCCTAC[C/T]CTGGGGCAATGGGAT | 9051 |
| rs376650402 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034539 | TCAAGATCCCTCAGG[A/G]TCTGGTCCAGTCTCT | 9051 |
| rs376655096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008479 | CAGTGGCACCGTGTC[A/G]GCTCACTGCAACCTC | 9051 |
| rs376692150 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026197 | CAGAGGCTGGCAGAT[G/T]CTTGTCAGGGAGGCT | 9051 |
| rs376758207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002617 | CCCATTCCACAGGAC[A/G]TGGCCGGCTGCTCAG | 9051 |
| rs376761098 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993403 | CCTGGCTGGACAGGT[A/G]CAGTTGGGAAAGGAA | 9051 |
| rs376906072 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017133 | CTCCCCTGGAGTAAG[C/T]CTGCGTGCAGTGCCT | 9051 |
| rs376968033 | snp | G/T | 7.85207e-05 | 0.00626531 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018273 | TGGGCAGGCCATGGG[G/T]AGCGCAGGCAGGAAG | 9051 |
| rs377001946 | snp | C/T | 1.66463e-05 | 0.00288494 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025263 | TCTCCTCCTCCTGAC[C/T]TGGACCCATCTGTTT | 9051 |
| rs377006780 | snp | A/C/G | 3.37811e-05 | 0.0041097 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037105 | ATCCTGGAAGGGGAG[A/C/G]ATGGCTGGTGGACTG | 9051 |
| rs377073641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005675 | ACCTTGTTCTACCTC[A/G]ATTCTACTTTCTAGC | 9051 |
| rs377107761 | snp | A/G | 0.000163987 | 0.00905354 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018497 | AAGGAGCTGGTGCAG[A/G]TCGCACGGAAGGCAG | 9051 |
| rs377114025 | snp | C/T | | | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037143 | GAACGGGCAGCGTGG[C/T]TTCGTCCCTGGTTCC | 9051 |
| rs377192593 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021024 | TCTATGGGATGCTCA[C/T]TCCCTGCCCCTTGCA | 9051 |
| rs377214787 | snp | C/T | 0.000438185 | 0.0147953 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035834 | ACCCCCACCCCCGAG[C/T]GGAATGAGGGTGTCT | 9051 |
| rs377240256 | snp | C/T | 3.92611e-05 | 0.00443046 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028566 | CAGTCCAAGAAGACA[C/T]ACGAGCAGAAGTGCC | 9051 |
| rs377256004 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021259 | AACAGGAGGTTACAT[C/T]TTAAGTGATTTTTGA | 9051 |
| rs377334374 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028390 | CCCCACGCCTTCTCT[-/T]ATCTCCTTCCGGACC | 9051 |
| rs377354932 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010603 | CATCTACCTCTGGCC[A/G]CCTTGTGTTTGCTCC | 9051 |
| rs377374701 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023649 | TGCTGAGTCCGGTTT[C/T]GGACACGCTGAATTT | 9051 |
| rs377437961 | snp | A/G | 0.000699755 | 0.0186919 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032879 | CCGGTGCCCTACCAG[A/G]ACTATTACGATCGGG | 9051 |
| rs377439325 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031795 | GATGGATGCAGCCCA[G/T]CACACGGCTCTCCCG | 9051 |
| rs377441775 | snp | C/T | 0.000317949 | 0.0126045 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018406 | CAAACCTGGGCCTCC[C/T]CCAGAGGTGGCAAGT | 9051 |
| rs377473445 | in-del | -/GAAA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004896 | AAAAAAACAAAGAAA[-/GAAA]AGAGAAGCAGAGAGC | 9051 |
| rs377512417 | snp | A/C | 8.63297e-05 | 0.00656943 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018411 | CTGGGCCTCCCCCAG[A/C]GGTGGCAAGTCACTG | 9051 |
| rs377610017 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030459 | AGTACAGGGGTGGAG[A/G]AGCTCGTGTCAGGGC | 9051 |
| rs377712845 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010773 | CTGCCTCACCCTCCG[A/T]GTAGCGGGGATTACA | 9051 |
| rs377714305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026798 | TCTCTGAGCTGGGAC[A/G]TGCCCGCAGAGCCTG | 9051 |
| rs377719165 | snp | C/T | 1.6643e-05 | 0.00288465 | stop-gained, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025318 | GACTCCTTGAAGCAG[C/T]GTAAGTCCCCTACCC | 9051 |
| rs377721832 | snp | A/C | 1.75891e-05 | 0.00296551 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035824 | AGAGACCCTGACCCC[A/C]ACCCCCGAGCGGAAT | 9051 |
| rs377763211 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014665 | AAAGGGGGAAGTGGC[A/G]GTAGTTACAGAGGGT | 9051 |
| rs386383532 | in-del | -/TA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000470 | GAGAGATATATATAT[-/TA]ATATATACACACACA | 9051 |
| rs386785513 | in-del | C/TG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034201 | TGGGGAAAAGAGGTG[C/TG]GGGGCACGCAGCACA | 9051 |
| rs397687061 | in-del | -/A | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004701 | TAAAAAAAAAAAAAA[-/A]GTACAAAAATTAGCT | 9051 |
| rs397813104 | in-del | -/C | 1.82061e-05 | 0.00301708 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035769 | CCAGTGTCCCCAGAA[-/C]GGGGAGGGGTCTATG | 9051 |
| rs527354872 | snp | C/T | 0.000594732 | 0.017234 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028610 | CGCGGAGCAGGCCTT[C/T]GAGCGCATTAGCGCC | 9051 |
| rs527511934 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036715 | AAAGGGGAGGCTTGT[C/G]GTAAGCTTAGGCATG | 9051 |
| rs527578859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003525 | GCGGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 9051 |
| rs527619029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032155 | GCTGTCAGCCAGGGC[C/T]GTGACCCCTCAGGAT | 9051 |
| rs527679453 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037298 | GAGAGGGAGCCTGTC[A/G]TCTCCCAGGGAATAA | 9051 |
| rs527712041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005302 | GAGGCAGGAGAATTG[C/T]TTGAACCTGGGAGGC | 9051 |
| rs527716587 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037608 | CAATGGGGAGAGCAG[A/G]CTTCTTGGGGGCGGA | 9051 |
| rs527766714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031108 | AGCTCCGGCTGAGCT[A/G]TGAATGGGGCCCAGC | 9051 |
| rs527797602 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033718 | GGCTGATGCAGTTCC[C/T]GGCCCTTCCCAAGGA | 9051 |
| rs527997972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011407 | CATCTCTGGGACTCG[G/T]CCAGCTGGGCTGCTC | 9051 |
| rs528030214 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017000 | GGGACTTCTTCCTCC[A/G]GTCTCTGAGGCTTTA | 9051 |
| rs528079189 | snp | C/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993205 | TGCTGGGTAAGTACT[C/G]CAAAGCCGAATTGGC | 9051 |
| rs528087919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014296 | CTGTTCTCACCTATG[C/T]GCACGATTTCACTTG | 9051 |
| rs528129165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001549 | CTCAGAGCTTGCAGA[C/T]AGTGCAGGAGGTGGG | 9051 |
| rs528172677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014861 | GTTTCCTCCCAAGAG[C/T]CTCCTCCTGGAGTTC | 9051 |
| rs528187669 | snp | A/G | 0.000337645 | 0.0129888 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035902 | GGCCTCACCAGCCCA[A/G]GAGTACCGGGCGCTC | 9051 |
| rs528260508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025488 | ACCAGTATCCATGCT[C/T]TGCCCCCAGAAATGG | 9051 |
| rs528351530 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996283 | CATGAAATAAGGGCG[C/T]CCAGCCAGTGGTAGA | 9051 |
| rs528409018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007816 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 9051 |
| rs528463432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021044 | TGCCCCTTGCAGAAC[A/G]GGCAGGGGACTGGGG | 9051 |
| rs528614210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036253 | CGTGGAGCACATGTA[C/G]CTATGCCGTCCACAC | 9051 |
| rs528617154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009808 | AACCCAGTGCCTGAG[A/C]CCTGTCACGCCCCAC | 9051 |
| rs528659128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031099 | GGCCTGGTCAGCTCC[A/G]GCTGAGCTGTGAATG | 9051 |
| rs528664564 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001081 | ACAGTTCTCTAGCTT[A/G]TGAATTTGGTGACCA | 9051 |
| rs528670572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031423 | GCCTCAGCAGCTCAG[C/T]CTTTGCCCCCAGAAC | 9051 |
| rs528695291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026257 | GGAGGGCAGGCAGGA[C/T]GCAGACTGGCCTGGA | 9051 |
| rs528726788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996430 | CCAGGGCTCTGGGGA[A/G]AAACTGAGACCTCTC | 9051 |
| rs528984283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031492 | TCTCTGCCTGGAAGA[C/T]GATGACTCTGTGGTT | 9051 |
| rs528995307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997024 | CTGTCCAGTCCTAGA[A/G]CCCCTGGGCCTGCCT | 9051 |
| rs529003530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036625 | ATGAGGCCAGGGCTC[A/G]GGGAGGCAGGGAAGC | 9051 |
| rs529061462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020405 | AGGACAAGCAGAGAG[C/T]GCCAAGCCACAGGGG | 9051 |
| rs529122841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014333 | GGGTCACCTCTAGGC[G/T]GTGAGAACTATTAGG | 9051 |
| rs529144042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014810 | ACAGGGCACCCAGGC[C/G]TTGGCCACACTGCCT | 9051 |
| rs529366933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003248 | ATGATGGAGGGAACT[C/T]TGGGTGGAAACCAAG | 9051 |
| rs529402949 | snp | A/G | 0.00212917 | 0.0325585 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037059 | GAACCCAGATGAGCT[A/G]GACCTGTCCGCGGGA | 9051 |
| rs529452044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027121 | GGGTGTTTTGTGCTG[C/T]GTGTGTGTGAGTGCC | 9051 |
| rs529494138 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021188 | TTTCTGCAGTCCCCT[C/G]ACCTCAAACCAGCCG | 9051 |
| rs529653444 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031133 | CCCAGCCTGGCCGGG[A/C]CCTGCAGCCGCCTCC | 9051 |
| rs529673937 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018369 | AACACGCCCTGCTTT[A/T]AAAAACTCTTCTGTG | 9051 |
| rs529760185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012515 | CCCATCCATCCATCC[A/T]TCCATCCATCCATTC | 9051 |
| rs529770733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013181 | AAAGCTGCTGCTACG[A/T]CTTGCTTCCCCACCT | 9051 |
| rs529834707 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029439 | CCCCCCAGGGTGGCC[C/G]GGGAAGCTTGACAGT | 9051 |
| rs529846818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029714 | CATTCCAGATATGTG[C/T]CGTCAAAGTAAACGC | 9051 |
| rs529985694 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013952 | GAGGTGATGAGGTGA[C/T]TCATTTCTTCCAGCC | 9051 |
| rs530110553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030702 | ACCTGTTACTCACTC[A/G]TTTATTCAGCCTCCT | 9051 |
| rs530187326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026123 | ATATGTAGGGCATGG[C/T]TGTCCCGAGACAGAG | 9051 |
| rs530322423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000877 | TATTTTAAATTTTAT[A/T]TTAAATTGTAGCGAA | 9051 |
| rs530330406 | snp | C/T | 0.000185237 | 0.00962206 | intron-variant, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026145 | GAGACAGAGTGACTG[C/T]ATGGAAGTGAAGTCC | 9051 |
| rs530336490 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995106 | CGAGGGCCCTGTGCC[C/T]GCCCCGGGGGAGGTT | 9051 |
| rs530353750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000081 | TGTGGGTGTATCTCT[C/T]CTTTGAGGCTGGGCT | 9051 |
| rs530357633 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001937 | TGTTTTTATACTGTT[G/T]GATTTTTGAACCATA | 9051 |
| rs530403937 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004244 | TTGCAGTTAATGGGA[A/G]GGTGTGTTGGTTTGC | 9051 |
| rs530419429 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994573 | CTTCAGAAGGGGGTT[C/T]TCTGCCCCAAACAGC | 9051 |
| rs530475106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007681 | CTCACTGCAAGCTCC[G/T]CCTCCTGGGTTCACG | 9051 |
| rs530506492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013229 | TTTCCCAGTCATCTT[C/T]AGGTGTAACCCAATC | 9051 |
| rs530567099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007133 | TTGCTCTGCCTTACA[C/G]CTCCCCAAGAAGGTC | 9051 |
| rs530609484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030314 | CAGAGCACAGTTGGG[A/G]AGCAGCAGCAGCACC | 9051 |
| rs530611280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024084 | ATGGGATAATAAAGG[C/T]ACCTGTGCTGGCAGA | 9051 |
| rs530623053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024711 | TCCCTGCCTCCTATG[C/T]GCAGTGCTGGGCCCT | 9051 |
| rs531047131 | snp | A/C | 0.000230168 | 0.0107253 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035853 | ATGAGGGTGTCTACA[A/C]AGCCATCGCAGTGCA | 9051 |
| rs531094000 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026276 | ACTGGCCTGGAGGCT[-/G]GGGCTTGGGCCTGTG | 9051 |
| rs531107972 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030974 | AGGCTGGGGCAGGGA[A/C]CCCCTGGGCATCTCC | 9051 |
| rs531132774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035398 | AGGGGCAGTCCCAGC[C/T]CTGGCAGAGCGCGTG | 9051 |
| rs531137475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031066 | CTCCTTTGGACTGGG[C/T]TTCCAGCAGAGAGGG | 9051 |
| rs531150198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030807 | GCAGGCATTCTTCCA[C/T]CCTCTTTGTTGAAGC | 9051 |
| rs531154096 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003571 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 9051 |
| rs531154710 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995201 | TCCAGCCTGCCTCTT[C/T]CACTGGCCACTGCCT | 9051 |
| rs531218741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995689 | GCAGGTGATGGGATG[C/T]GGCTCCGAGAGGGGA | 9051 |
| rs531324847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028710 | GGCAGTGGGGGAGGC[A/C]AGGAAGGGGTGCCGT | 9051 |
| rs531335418 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022878 | CCTGCCTGCCCAGGT[A/G]CCCCAGACAGAGGTA | 9051 |
| rs531339175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029359 | ATGGAGCTAGCCTGT[A/G]GTCCTCTGTGGGCGG | 9051 |
| rs531428108 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030784 | AGTCCTGGGCCCCTT[C/T]GTTGCAGGCAGGCAT | 9051 |
| rs531492060 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028926 | GCCCACAGGGTGATG[A/G]GAGCAGACGCCAACC | 9051 |
| rs531555108 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008168 | CAGGTGTGAGGTCTG[C/T]ACAGCACAGGGAAGC | 9051 |
| rs531567637 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037251 | ACTGTCCCCACCTTG[C/G]TAGGGCCCAGAACCA | 9051 |
| rs531570939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004183 | AGATGGATCGGACTG[A/G]GCTGGGCCTGGATGC | 9051 |
| rs531665750 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028080 | CGGGGCGCTTGGGCC[C/T]GTGCTGGGCGCTATG | 9051 |
| rs531723873 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994347 | AAATATTCTCGACAC[C/T]GTCTACTTTCCAAAG | 9051 |
| rs531734146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034706 | GTAAAGCTTCACTCA[C/T]CTTTGAAGACTCAGC | 9051 |
| rs531755708 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035663 | GAGGCCCTCAAGAGG[A/G]AGTGTGTGTCCCCCA | 9051 |
| rs531831589 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993716 | ACCTAGAGGCATCAT[C/T]CCATCTGATGGATGG | 9051 |
| rs531836633 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005523 | GTAATTATATGTAAC[A/C]TAAAATTGACCATTT | 9051 |
| rs531863806 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012211 | TCCATCCATCCATCC[A/G]TCCACCCATCTGTCC | 9051 |
| rs531896742 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999056 | AGCACTGAGTCTAAG[A/G]CGCTGGGAAGCCCAG | 9051 |
| rs531972361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011501 | CACTCTGGAAACTCA[G/T]TTCTAATCTCAAGGT | 9051 |
| rs532014562 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014545 | GTTAGCCTCCTGCCC[C/T]CACTTTCCCAATGAG | 9051 |
| rs532055152 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037634 | GCGGAGGGTTGAGCA[A/G]GTCCATGGCTGGGCA | 9051 |
| rs532174773 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037559 | AGGGGTGCAGGAGGA[C/T]GTGGCAGGGGCAAGA | 9051 |
| rs532174837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033213 | GAGCTCTGGGGAGGC[C/T]CCTATGCTGGCTTCC | 9051 |
| rs532211487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018323 | TCCTGGGACAGTGGA[C/T]GAGGCCCCCATCCCA | 9051 |
| rs532211613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011773 | TGAGTCCTCTCTGTG[A/G]AACCAGACCTGCTTA | 9051 |
| rs532218270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028756 | AGATCTGCATCTGGG[C/G]ATGCTGCTTAGCCCT | 9051 |
| rs532474791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030665 | TGCTTAAAGGGGCCC[A/C]AGTGAGGCAGTTGGG | 9051 |
| rs532500643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034868 | ATTCAGTAAACCTTC[A/G]TGACCCCAGCTCAGT | 9051 |
| rs532549063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030347 | CGTGGGTGGCCCTGA[C/T]GGGCATTCAGATGAG | 9051 |
| rs532612802 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024892 | TCCCCTGTAGCCTCA[C/T]CCTGGGGCCATTTGG | 9051 |
| rs532651482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006926 | TGTTTTGGCTCTTTG[C/G]GGGCCCGAGTAGAGC | 9051 |
| rs532737657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018717 | TGAGGGAGGAAGCCC[A/G]AGGGTCTGAGTTCTG | 9051 |
| rs532755399 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001064 | CCACTGTTCATGGCT[G/T]CACAGTTCTCTAGCT | 9051 |
| rs532782867 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006277 | ACCTTCTTTGGAGAA[A/C]GTCTATTTAAGACCT | 9051 |
| rs532870681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034328 | CTGGGGAGCTGGCAC[C/G]TGTGTCTGCCCGCCT | 9051 |
| rs532910548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027196 | GACCCCAGGCACAAA[C/T]TGGCTCAGTTCTCCT | 9051 |
| rs532956171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036686 | GGCAGTGGCTAGCTG[A/G]GGCTGGGGACCGCAA | 9051 |
| rs533009481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002370 | CTGGTGTCTATGGAT[C/T]TGGAAGTAGGATTCT | 9051 |
| rs533071764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996515 | GGACGCTCTGGCCCT[C/T]GGCTCAGCCGGCTGA | 9051 |
| rs533131872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016894 | AGACATGGGTCAGGG[G/T]AAGGAGTACCAGGCT | 9051 |
| rs533153026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010222 | GGGCGGTACAGAGCT[A/G]TGTAACCTGGACAAG | 9051 |
| rs533171772 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026951 | GCCCCGCAGGCAGAG[A/C/T]GCTGTGTTGTAGTGT | 9051 |
| rs533264055 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037285 | GTCCCCCAGCCCCGA[G/T]AGGGAGCCTGTCGTC | 9051 |
| rs533349129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022138 | GAGATTTTTAAAATT[A/T]TTTTCATGGTCTCTC | 9051 |
| rs533410768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016146 | CCCCTGAGAGTCCGG[A/G]TTCTTGTCCTGACTC | 9051 |
| rs533419248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004306 | GAACAGGCAGGAGAG[C/T]GACAGCTCCTTCCAC | 9051 |
| rs533441947 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023855 | AACTGAATGAGTGGG[A/G]CTGAGCTGAGGGGTG | 9051 |
| rs533507893 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026591 | GGAGCTCAGCCCAAG[A/C]CATGCGCCCCTCAGT | 9051 |
| rs533558143 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029347 | CGTTCTCTTTCCATG[C/G]AGCTAGCCTGTGGTC | 9051 |
| rs533562034 | snp | G/T | 0.00159617 | 0.0282053 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027858 | CCCCTGCAGTATGAG[G/T]CCGTCATGGACCGGG | 9051 |
| rs533612498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015749 | GTGAAGGAGGAGGGC[A/G]CGGGCTGGGGGAAGG | 9051 |
| rs533671057 | in-del | -/ACTC | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030694 | GGGAAGGTACCTGTT[-/ACTC]ACTCGTTTATTCAGC | 9051 |
| rs533790009 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021842 | CACCCATCCCTCAAG[C/G/T]CCTGCCTGAAATGTC | 9051 |
| rs533876793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026923 | CAGAGCATTCTTTCT[C/G]CAAGTGGCCAGGGCC | 9051 |
| rs533890019 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032604 | TGGCACTCAGAGGAA[C/G]AGGTGGGGATGGGGA | 9051 |
| rs533951956 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033267 | CCTGGTGCCCTGTCA[C/G]GCTGCAGTGGCAACG | 9051 |
| rs533951973 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028279 | GGGGCGTGGCGAGGG[C/G]CGTGCCCTCGCCGAA | 9051 |
| rs534026182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996581 | TCCTGGGGCTGCAGC[C/T]AGGAGGATGAGAGCT | 9051 |
| rs534113157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009986 | CATTCGGCAAGGAGC[C/T]GTGCTCTTCCTGTGA | 9051 |
| rs534135918 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024305 | CCCCACCGATCTCCC[C/T]CAGGCCTGGATCCCC | 9051 |
| rs534175994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003419 | GGCTTCTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 9051 |
| rs534187469 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997515 | TATTCACTCATTCAA[G/T]CCTTCAAACACATGC | 9051 |
| rs534195842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036852 | GGTTGGGGGAGAACT[A/G]TGATGACAAACTGAG | 9051 |
| rs534309876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035132 | GGAGGGTGAGGACTG[G/T]GCATCTTCCCACGAG | 9051 |
| rs534341498 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033507 | GTGACGAAGGTGACA[A/G]CCCATTGGGAGCACT | 9051 |
| rs534349577 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011139 | CTTGGTCAAAAGCCA[G/T]ACGCCCCACAACATT | 9051 |
| rs534445257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030869 | TCTCTGGGTGCTGCC[A/G]ATGGACAGGGCCTGG | 9051 |
| rs534554940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013293 | TCAATTTAAAGCTCC[C/T]CAGTTCCCCGACTTT | 9051 |
| rs534572347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007235 | GGCCTGGAGGCTGGG[C/T]CACCAACTTCCTCAG | 9051 |
| rs534702768 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995387 | AACAAAACAGGTTGA[A/G]CTTTTTCCTCCCCTC | 9051 |
| rs534732228 | snp | C/T | 0.000185615 | 0.00963187 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994821 | CTAGACCTGGGTAAG[C/T]CCCTCCAGAATGACT | 9051 |
| rs534766367 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001897 | AGGGATGAGGCTGAG[C/T]GGCTGTGAACGTTTT | 9051 |
| rs534863841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006540 | TTAAATATCATGAAG[C/G]TTTCCCTATGTTTTC | 9051 |
| rs534878256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999745 | CGGGGCTGGAGGAAT[A/G]ACTGGGTCAGGCAAG | 9051 |
| rs535003999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014452 | CCTCTCAAACAGGCC[C/T]GAGTACCCTCTCTGA | 9051 |
| rs535038597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030904 | CAGGGCTCAGGACTC[A/C]CGTCCGAGGTCCCTC | 9051 |
| rs535062164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008558 | GGGATTACAGGTGCC[C/T]GCCACCACACCCGGC | 9051 |
| rs535138851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002399 | CTCTCCATCCCCCAT[A/C]TAATTTTCTGCAAGT | 9051 |
| rs535256490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007364 | TGTAATTCCAGCACT[C/T]TGGAAAGCTGAGGCA | 9051 |
| rs535299704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020632 | ATAAAGGGCTTTGCC[A/T]TTCCTTAGCCAGAGT | 9051 |
| rs535312648 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997508 | GTATGCATATTCACT[C/T]ATTCAATCCTTCAAA | 9051 |
| rs535394390 | snp | A/G | 0.000100015 | 0.00707089 | synonymous-codon, nc-transcript-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77035520 | CAGGTTCTCTGGACT[A/G]CTGCACGGAAGTCCC | 9051 |
| rs535408605 | snp | A/T | 0.000333167 | 0.0129024 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995436 | CGTGGCTGCCTTCTG[A/T]GTGTTGCAGACGGCG | 9051 |
| rs535531018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996653 | GGGCCTGTGGCCAGC[A/G]TGTGAGTGTTCTGCT | 9051 |
| rs535550373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036459 | TCTGATGTCCATAGG[A/G]TGAGGATGAACCAAG | 9051 |
| rs535567788 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019976 | AAAGAGAGGGTACCT[C/G]ATGGGGAGAACTCAG | 9051 |
| rs535615488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031757 | GCAGAGAGGGCCCCC[A/T]GCCAGGGTCCCTGAG | 9051 |
| rs535671830 | in-del | -/TTTAA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002311 | TGTTCTTGCTTCTAC[-/TTTAA]TTTGTGTAGGATGAA | 9051 |
| rs535675331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014506 | TGTGCCCTAGAGGGG[C/T]GGGCTGTCAGGGCCC | 9051 |
| rs535684747 | snp | C/T | | | splice-donor-variant | PSTPIP1 | GRCh38.p7 | 15:77027916 | AGAAGGCCATGGAGG[C/T]GAGCGCCAGGGCCTG | 9051 |
| rs535702994 | snp | A/G | 0.00352014 | 0.0418052 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994847 | TGACTTGCTAGTGCG[A/G]GGTGGGGAGTCTGGC | 9051 |
| rs535713285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035163 | GCCTCAGTGCGGAGG[C/T]CCTAGAACCCCCAAA | 9051 |
| rs535803282 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008842 | GACTCTAAGTAGAGT[C/T]GTGTTTCTCCACCAT | 9051 |
| rs535827686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001968 | TGAATGTATTAATTA[C/T]TCAAAAATTAAATCA | 9051 |
| rs535869161 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010818 | CGCCCAGCTAATTTT[A/G]TATTTTTAGTAGAGA | 9051 |
| rs535890888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002524 | ATTTGTGGTTTGCTA[A/G]CATGCCCTTTTCCAC | 9051 |
| rs535961552 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029476 | AGGTCTGCTGGGGTG[A/C/G]GCCCTGGCTCCTGGG | 9051 |
| rs535969237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997314 | CAGGAAGGGGAGAGA[A/G]GTAGCCAGTGGGAAC | 9051 |
| rs536111717 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015281 | GGTATATGGCTTTGG[A/G/T]GACAGGTTGACCTGC | 9051 |
| rs536121189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008570 | GCCCGCCACCACACC[C/T]GGCTAATTTTTGTAT | 9051 |
| rs536180052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036962 | GCCGCATTTACTGCT[A/G]GGTGGGGGAACGCCA | 9051 |
| rs536238421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004630 | AGGCTGAGGTGGGAA[A/G]ATCACTTGAACCCAG | 9051 |
| rs536240279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011892 | CCTTGCATTGTCCTG[A/G]AGTTGGCCTCCCTGT | 9051 |
| rs536253089 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036618 | TCCACTGATGAGGCC[A/G]GGGCTCGGGGAGGCA | 9051 |
| rs536302980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005810 | TCCATGTCATAGCAT[A/G]TGTCAGAATTTTCTT | 9051 |
| rs536360451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033871 | CAGTGACCCCAGGAG[A/G]CAGCACACCCGCAGC | 9051 |
| rs536369985 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993388 | TCCATCCGGGGCTGC[C/T]CTGGCTGGACAGGTA | 9051 |
| rs536508173 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015920 | TCCTGGAGCCTGCAG[C/T]CTCTGGGGACTTGAG | 9051 |
| rs536682385 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006137 | TCTTGTTAATTTCTG[-/T]TTTTTTTTTAAATCA | 9051 |
| rs536829888 | snp | C/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037504 | TGCTAGGAGCTCCCA[C/G]ACTGCCAAGGAGACA | 9051 |
| rs536942315 | snp | C/G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013179 | CCAAAGCTGCTGCTA[C/G/T]GTCTTGCTTCCCCAC | 9051 |
| rs536945992 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035724 | CAGGGCCCAGCATGG[A/T]GAAACCCCATTCTAG | 9051 |
| rs536948997 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037761 | GATGGATCTGTTGGA[A/G]AGGCCATGGTGGGAG | 9051 |
| rs536982840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024348 | GGCTACTGCTCCTCC[G/T]TGGCCTCTGCTTCCC | 9051 |
| rs537052049 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013817 | CCTCCAAGGTTGGAG[A/G]CTTAGCTGTCCTCTG | 9051 |
| rs537068259 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005920 | GCTGTTTCTTTGAGC[C/T]ACTGTGAATAATGCT | 9051 |
| rs537101069 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994147 | GAGGGTGGTGATTTG[A/C/T]GGACAATCCCTGACT | 9051 |
| rs537117603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007982 | TGCCCATTGACCTGG[A/G]CCAGCTCTGAGCCCA | 9051 |
| rs537123971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034437 | GCCCTCGGCGCCTCA[C/T]GTGGGAAAGGCCCCC | 9051 |
| rs537159004 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76994727 | GCACAGCTGTGTCTG[C/T]TCCCAGACTATGGGC | 9051 |
| rs537187328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030151 | GACCCAAGCCTGTGG[A/G]ACTCCACCCCTCCTC | 9051 |
| rs537436588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015875 | GCCCCTGCCAGCAGC[A/C]CAAAGCTCTGAGCGG | 9051 |
| rs537444496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009998 | AGCCGTGCTCTTCCT[G/T]TGAAGACGCCTGGAC | 9051 |
| rs537620912 | in-del | -/CACACACACCTCCTCACCCTGGGGA | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029630 | CTGGGCGGTACTCCC[-/CACACACACCTCCTCACCCTGGGGA]CACACACACTCCCCC | 9051 |
| rs537728371 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027110 | CCTGTGCACTTGGGT[A/G]TTTTGTGCTGTGTGT | 9051 |
| rs537768753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019126 | AGGGAAGTGGCTCTG[A/G]TGAAGCGGGAGTCTC | 9051 |
| rs537768857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025663 | AGCCTCTCAGTTGCT[A/G]TGGGGGTAGGGGGCT | 9051 |
| rs537848980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033737 | CCTTCCCAAGGACCA[C/G]CTCATTCCAGGGCCT | 9051 |
| rs537862586 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023177 | TGAGAAAATTTAGAT[G/T]ATGAGCCTGGGGACA | 9051 |
| rs537877574 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993229 | AATTGGCTGTCTGGT[C/G]GCCCAGCCTGGGGAC | 9051 |
| rs537961682 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006825 | TCCTTATGACACTAC[C/T]GCACTACTTCAATTA | 9051 |
| rs537975756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023512 | TAAAATAGAAGGTGG[C/T]GGCAAGGAAGGGAGA | 9051 |
| rs537981558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017527 | CCTCCCTGGATCTCC[A/G]TGAGGGGGGGTTTCC | 9051 |
| rs538025146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003838 | GGGGCGGCTCAGGGC[A/C]GTGCTAAGGGACCAC | 9051 |
| rs538032246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011087 | TCATCATTGAGAAGG[A/C]CTATTTAAAAGAACA | 9051 |
| rs538042433 | snp | C/T | 0.000424259 | 0.0145585 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037158 | CTTCGTCCCTGGTTC[C/T]TACCTGGAGAAGCTT | 9051 |
| rs538055251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027463 | GGCCTGTGTGCCTCC[A/G]AGTTAATGTGGAACT | 9051 |
| rs538074631 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031388 | CCTCTGTGATCCAAG[C/G]CTGGCCCCAGGGGTC | 9051 |
| rs538089306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004529 | GCTAGAGAGAGTGAC[A/C]AAGGTGGAGAGTAGT | 9051 |
| rs538133422 | snp | G/T | 0.000121264 | 0.0077857 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032817 | TGGCAGGGCCAGAAT[G/T]GGGTGTTGGGGGCCG | 9051 |
| rs538137417 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029177 | GACAGGAAGGCTGAG[G/T]CCCAGAGAGGGAAGT | 9051 |
| rs538172329 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021890 | GTCACCTCCACTCCC[C/G]TATTGCTCATCCTGC | 9051 |
| rs538233460 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010616 | CCGCCTTGTGTTTGC[C/T]CCTTGCCTCCTCTCT | 9051 |
| rs538239361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010435 | GTCCTGCCCTTTGCT[A/G]TGTGTGACTTGGCTC | 9051 |
| rs538335440 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010970 | TTTTCTGCATGTTTT[G/T]GTTTCATGACACAGG | 9051 |
| rs538367365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998758 | GTCCTGTCCCTCAGT[C/T]GGCCTGTTTTTGCAA | 9051 |
| rs538504370 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037341 | TGTTCTCCTTGGTGT[G/T]CTGGGGTCCCGTTCT | 9051 |
| rs538664638 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024190 | AGGAGGTCGGGGAGG[A/C]GCCTGAGAATCTGTA | 9051 |
| rs538667821 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035150 | ATCTTCCCACGAGGC[C/T]TCAGTGCGGAGGTCC | 9051 |
| rs538673788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011216 | GACAGTAGCTGCCTC[A/G]TGGTCAGTATTGCTG | 9051 |
| rs538685948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004550 | GGAGAGTAGTTGGAG[A/G]TAAGGTAAGAAATAG | 9051 |
| rs538742934 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037397 | GTGCTCAGTTCAGAG[A/G]AGGCAAAGGAACAAG | 9051 |
| rs538826875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028212 | TGAGCTTGATCCTGC[A/G]AGACGCTGGACAGGA | 9051 |
| rs538846070 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022277 | CCTCAGCACAGGGAG[C/T]CGAGAGGGCTACTCC | 9051 |
| rs539021956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023620 | CCTGGAAGAGGAGAG[C/G]TTTGCAGGGCAGGTG | 9051 |
| rs539056549 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020877 | CTCCTGTGGGGGGGG[A/G/T]GGGTGTGTGTGTTGG | 9051 |
| rs539225380 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037700 | GTGAGGTTGGGGGTA[C/T]ACCCAGGAATATTCG | 9051 |
| rs539263059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033765 | CCTCAGGAGCCCCTG[C/G]AACTTCCTACTCCTG | 9051 |
| rs539290976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001762 | GTTGTGAAAAGTGGG[G/T]AAATAAGCATTTATA | 9051 |
| rs539299945 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016701 | GGAGTTTGTGGGGAG[C/G]GGGGGCACTGTTGGG | 9051 |
| rs539635591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015355 | GGCAGTCTCTTTCCC[G/T]GTTTGGGCCTCCTGT | 9051 |
| rs539647104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015702 | GAGCACGGAGTCAGA[C/T]CCATGCCCTCGAGGA | 9051 |
| rs539670123 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035996 | CCTGAGAGCTCCCTC[G/T]CCCATCCAGTGCCTT | 9051 |
| rs539796536 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003037 | GCATTGTGCAAGGTG[A/G]CTGGTAGGAAGGGAA | 9051 |
| rs539799949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003274 | CCAAGACTGCCTCTG[C/T]TTCCAGCTAGAGAGC | 9051 |
| rs539837909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014720 | TGTGGAGGGCCCTGG[A/C]CGGCTCACAGGCCTG | 9051 |
| rs539885253 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997462 | AACATTTGCTGAGCA[C/G/T]GAAAGATGTGCCAGG | 9051 |
| rs539895526 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997828 | CACACTACTCTGGCC[A/G]CAGGTGTTATATTAG | 9051 |
| rs539914837 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009434 | GCAGGCACCTCATAT[A/C]AGCCCTATAAGGGCT | 9051 |
| rs539921783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002214 | CTAGGCCCAGACGAG[G/T]GTCACCTGTGCAGGG | 9051 |
| rs539930606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025656 | CATTGCCAGCCTCTC[A/G]GTTGCTGTGGGGGTA | 9051 |
| rs539958477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032509 | CACAGCTCCCTTCAG[A/G]GCAGAGAAGCCCTAG | 9051 |
| rs540075313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020336 | GTCTCTGAGTCCAGG[G/T]TCTGTACCTATGGAA | 9051 |
| rs540092791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009918 | GACGGGGATGTGCAA[A/T]GACAGTGCCTGGACC | 9051 |
| rs540169857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014306 | CTATGCGCACGATTT[C/T]ACTTGCTTCTCGGGT | 9051 |
| rs540442170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026596 | TCAGCCCAAGCCATG[A/C]GCCCCTCAGTCTCCA | 9051 |
| rs540457513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996448 | ACTGAGACCTCTCTG[G/T]TTGGAGCTGGGGAAT | 9051 |
| rs540497544 | snp | A/C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021989 | GGAAAACCAAGGCAA[A/C/G]GCCAGCTTCCTGTAG | 9051 |
| rs540568190 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009151 | GGATAAGGAGCCCCA[C/T]GTGCCATCCCCTGCA | 9051 |
| rs540606788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028713 | AGTGGGGGAGGCAAG[A/G]AAGGGGTGCCGTAGA | 9051 |
| rs540628243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030222 | CTCTGGAAAGTGAGG[C/T]GGGGCGCCCAGAGAT | 9051 |
| rs540639859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022039 | GGGCAGGTACAGCCC[C/T]CAAGGGGTGCAAGTT | 9051 |
| rs540658514 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006683 | ATCCAGTTTTCCCAG[C/T]GCCATTTGTTGAAGT | 9051 |
| rs540691726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024504 | AGAGAGGCTGCAGGG[A/C]GAGCCAGATAAAATA | 9051 |
| rs540749497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015965 | CCTGCAGGGCCTCTC[A/G]CTGCTTTCTGACTCC | 9051 |
| rs540801570 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034260 | CCCCCTGCCCTGGCC[A/G]CTTCCTCCACCTGTC | 9051 |
| rs540838368 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002293 | CCTGAATTCTAGAGA[A/G]TTTGTTCTTGCTTCT | 9051 |
| rs540849970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006029 | CTGGATCATATGGTA[A/G]TCCTATGTTTAACTT | 9051 |
| rs540869864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996845 | CCAGGATGCTCAGGG[C/T]CCAGGCTGGCAGCTG | 9051 |
| rs540915310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999339 | GCTGGAGGGCAGTGG[C/T]ACAATCTCAGCTCAC | 9051 |
| rs540932134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034588 | ACACACCCAAATTGG[C/T]CCACTCCACTCCACA | 9051 |
| rs540938380 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032747 | AAGACAGGCACCTCC[C/T]CAGGCACCAGGATGG | 9051 |
| rs541064827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022788 | GCCTGATGGTTCCAG[C/T]AACGGGGACAGGGGA | 9051 |
| rs541075209 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995077 | GGGAGCACAGCAACT[C/T]CACTTCCTGTGGGCG | 9051 |
| rs541085532 | snp | C/T | 0.000597729 | 0.0172774 | missense, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995578 | GACGCCTGAGGATGA[C/T]GCCCCAGCTGCAGTT | 9051 |
| rs541159589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018760 | GCAGGGGAGACAGGA[G/T]GCCATCCATCCTCAG | 9051 |
| rs541337933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007580 | TGCCACTGCACTCCA[A/G]CCTGGGCAACAGAAC | 9051 |
| rs541356824 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994169 | TCCCTGACTCACCCC[A/T]TTTTGCCAGCCTGCC | 9051 |
| rs541460280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001260 | TGGCTATTTTCCAGG[A/G]AAGGAGGCATTTCTG | 9051 |
| rs541478908 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019322 | GACCACCGGCCTCCA[A/G/T]CTTCTTGAAAGGGCT | 9051 |
| rs541510245 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012699 | CTGTGCCTCTGTTTC[C/T]GTATCTATACAATGG | 9051 |
| rs541583620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030958 | GGTGCAGCCTGAAGG[A/G]AGGCTGGGGCAGGGA | 9051 |
| rs541591360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013523 | TTTCTCTCCCTGGCA[C/T]CTGGGCAGGTTTTTT | 9051 |
| rs541638561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013134 | GGGAGGAGAGCACCC[C/T]AGCACCATGCAGCTC | 9051 |
| rs541638695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019278 | ACTGTCCCCCTGGGT[A/G]AGGACAGAGCCAGGC | 9051 |
| rs541689842 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007470 | AAAATTAGCTGGGGC[A/G]TGGTGGTGCACACCT | 9051 |
| rs541697144 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994259 | GCTGGGGCTGGGGCT[C/G]TAGTCCAGGGCTCTT | 9051 |
| rs541754865 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002623 | CCACAGGACGTGGCC[A/G]GCTGCTCAGGTGTTA | 9051 |
| rs541761213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024625 | CTCAAAAAGTGCTCG[C/T]TCATCTGAGATTCAC | 9051 |
| rs541765483 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018934 | AGGGGTCCAGGAGGG[G/T]ACACACCTGGGTTCC | 9051 |
| rs541984448 | snp | C/T | 0 | 0 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993684 | TCTGTTAACAGAGGG[C/T]CTCTAGTCTGCTCCA | 9051 |
| rs541990222 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025845 | AAGGTCCTTCCTGTC[A/G]AGCTGCCTCACGCCT | 9051 |
| rs542018257 | snp | C/T | 3.7165e-05 | 0.00431059 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030504 | CCTGCGCTTTCAGAG[C/T]GGGTATACAGGCAGA | 9051 |
| rs542049942 | in-del | -/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994348 | ATATTCTCGACACCG[-/T]TCTACTTTCCAAAGA | 9051 |
| rs542126867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023455 | GGCAGGGGCTGCAGC[A/G]GTGGTGGCAGCTAGC | 9051 |
| rs542140044 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998568 | GCAATTAGTGGCAGT[A/C]TGCACAGTACCTGAT | 9051 |
| rs542209542 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031035 | CGGAGTCGGGATGGG[A/G]ACCCCAGGGCACTCT | 9051 |
| rs542286074 | snp | C/G/T | 0.000866847 | 0.020801 | missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031224 | GACCATTCTCCGCAA[C/G/T]GCCCTGTGGGTGCAC | 9051 |
| rs542414752 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013271 | AGTATCACAATTTCA[C/T]TCTCATTCAATTTAA | 9051 |
| rs542454041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016612 | GAATTTCTAGGGATG[C/T]TTATGGAGGGGGTAG | 9051 |
| rs542610612 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033006 | GCCAGGAAGTGGGTC[A/G]AGCCCCTCCTCTGCA | 9051 |
| rs542615022 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006147 | TTCTGTTTTTTTTTT[A/T]AATCATAGCCACCTT | 9051 |
| rs542724631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033393 | TAGTGCTGGGCCTCA[A/G]TGTGTGACCTGGGCA | 9051 |
| rs542724680 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028643 | CGGCCACCAGAAGCA[A/G]GTGGAGAAGGTGCGC | 9051 |
| rs542786002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029290 | CCTGTGGGTTGTGGT[C/T]TCACTCTTCACAGGC | 9051 |
| rs542833410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010102 | CTGCATCAGTCACCC[C/G]CAAGGGCCCACGGCC | 9051 |
| rs542853723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010651 | TTTCTTCTCTTTTCT[A/G]TTTCTTTTTCTTTTG | 9051 |
| rs542916916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004176 | GCCACACAGATGGAT[C/T]GGACTGGGCTGGGCC | 9051 |
| rs542940166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011414 | GGGACTCGGCCAGCT[A/G]GGCTGCTCAGGTGAG | 9051 |
| rs543015039 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009629 | GCCCTTCCAGGAGCC[C/T]GGTGAGCGTCAAATG | 9051 |
| rs543075797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029628 | GCCTGGGCGGTACTC[C/T]CCACACACACCTCCT | 9051 |
| rs543079840 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034485 | TGCAGGGCTGCCCCC[A/C]ACAGGCCCCTGAGTC | 9051 |
| rs543092226 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993429 | AGGAAGGCCTCATGT[A/G]TGGGAGCCTTGAGGT | 9051 |
| rs543223682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017770 | CTTAGCTGAGATAGG[A/G]ATATTGGAAGGGTGG | 9051 |
| rs543245476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011352 | GTCCCTGTCAGCCAC[A/G]GGCCTGTGGGCCTCC | 9051 |
| rs543415753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999937 | TCCTATTCCTTTTAG[A/G]GTAGTTAAAAGGAAA | 9051 |
| rs543422331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999286 | ACTTCATTTCACTTT[G/T]TTTTTTTTTTGAGAA | 9051 |
| rs543525649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021001 | GAGGCCCACAGCTGC[C/T]CCCCAGGTCTATGGG | 9051 |
| rs543545110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999730 | GCCATAGTTCAGTGC[C/T]GGGGCTGGAGGAATA | 9051 |
| rs543645716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998444 | CCTTAAAGCTCATAT[A/G]CTACACTCCTAGGAG | 9051 |
| rs543647921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004908 | AAAGAAAAGAGAAGC[A/G]GAGAGCCAGATCTTG | 9051 |
| rs543693641 | snp | A/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036301 | GTGCACACGTGCGGG[A/G]AGCTGGCAGAGCCTG | 9051 |
| rs543749761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033619 | TTCACATGGTGCCTG[G/T]GCCCCCACCGCCATG | 9051 |
| rs543786435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013032 | TACCTCAGGTTTTCA[A/G]TCCACAGAAGACAAG | 9051 |
| rs543809861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002867 | TACACAGAACTAGGG[C/G]AGCCCCTGGGATGGA | 9051 |
| rs543867889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003424 | CTTGGGAGGCCGAGG[C/T]GGGTGGATCATCTGA | 9051 |
| rs543890947 | in-del | -/GTG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020880 | CTGTGGGGGGGGGGG[-/GTG]TGTGTGTTGGCCCTC | 9051 |
| rs543937260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997038 | AGCCCCTGGGCCTGC[C/T]TTCCCTAGGGCAGAG | 9051 |
| rs543943354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030332 | CAGCAGCAGCACCAG[C/T]GTGGGTGGCCCTGAC | 9051 |
| rs543972298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031949 | TTGAGGTAGAAGGGC[A/G]AGCTCTGGACCCACT | 9051 |
| rs543985330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024430 | CCCCCTCCACCCAGG[G/T]CTGTCCGGTGGGCGT | 9051 |
| rs544009727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012241 | CATCCATCCATCCAC[C/T]CACTCATCCATCTAC | 9051 |
| rs544124364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006217 | CATTTCTCTAATAAT[G/T]AATGATGTTGAGCAT | 9051 |
| rs544131546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008921 | ATTTCCCAGACTCCA[A/G]CATAGAAGCCTTTAC | 9051 |
| rs544153950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022532 | TGCTCAGGGAGATCT[C/T]GACAGTTTCCCTGCA | 9051 |
| rs544189322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009550 | CTAGGATCAAACCCA[A/G]TTCTCCTTGTAAACG | 9051 |
| rs544288227 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020308 | CTTTGTGTGGCCCTG[A/G]ATGGTCCTCCCTGTC | 9051 |
| rs544344574 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036925 | TCCCCAAGGGGCTGC[C/T]CCTGCCCACCCTGGG | 9051 |
| rs544435223 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006397 | ATTTGTAAATATTTT[A/C]TCCCACTCTGGAGTG | 9051 |
| rs544479424 | snp | C/T | 0.000120504 | 0.00776127 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027784 | ATCCCAGGGACACTC[C/T]GTCCTCTTGGCCTAG | 9051 |
| rs544542897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028427 | TCCCTGTCCCTGGTG[A/G]GGATGCCCCCACTCC | 9051 |
| rs544544908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022073 | ATCCTCACGTCCCTG[C/G]CTCACCCCCAGTTGT | 9051 |
| rs544661666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998096 | TACAAAAATTAGCCA[A/G]GCGTGATGGCATGCT | 9051 |
| rs544721948 | snp | A/G | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010679 | TTGAGACAGGGTCTT[A/G]CTCTGTCACCCAGGC | 9051 |
| rs544883712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009726 | CTCATCCCGATCTCA[C/T]AGAGGAGGAATCTGG | 9051 |
| rs544973217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003469 | GACCAGCCTGGCCAC[A/C]ATGGTGAAACCCTGT | 9051 |
| rs545068883 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012164 | CCATCCATCCACCCA[C/T]CCACCCACCCACCCA | 9051 |
| rs545108125 | snp | C/G | 0.000310704 | 0.0124601 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032425 | CGGACAGCGCAGCCT[C/G]TAGGTGCATTGAGCC | 9051 |
| rs545209789 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016700 | TGGAGTTTGTGGGGA[-/G]GGGGGGCACTGTTGG | 9051 |
| rs545222701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015500 | CCACAGGCAGCATTC[A/G]GATGACAGAGGTTGG | 9051 |
| rs545414114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023207 | AATGAGGAGGAGAGC[C/T]AGGCATTGCCCCTGT | 9051 |
| rs545454932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005173 | CAGATCACCTGAGGT[C/T]GGGAGTTCAAGACCA | 9051 |
| rs545464910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014664 | AAAAGGGGGAAGTGG[C/T]GGTAGTTACAGAGGG | 9051 |
| rs545542379 | snp | A/G | 0.000546747 | 0.016525 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028534 | TGCAGCCCCCAAGTC[A/G]CGCCCCTCCACACCC | 9051 |
| rs545694054 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998326 | ATACAGAACACGGGG[C/T]GGAGGAGGGGAGCCA | 9051 |
| rs545727451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019453 | CCATACTCTGAAGGT[A/C]CCCCAAAGACACCAG | 9051 |
| rs545780966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036441 | TCGTGCCAGGATTGA[C/T]TTTCTGATGTCCATA | 9051 |
| rs545839288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026678 | GGCTGCCCGTGCCAC[A/C]TGCCCATCTGCCAGC | 9051 |
| rs545839960 | snp | A/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037706 | TTGGGGGTACACCCA[A/G]GAATATTCGGAGGAC | 9051 |
| rs546090571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036508 | TGAGAGTCCTTTCTG[C/T]TCCCTGCTTGAGGGG | 9051 |
| rs546185050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008376 | CTCCCAGTCCTCAAG[A/G]GAAGGAGCTTGCACT | 9051 |
| rs546198880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996711 | AAGGACCCCACGTGG[A/G]GAGGGCACCTTGTGC | 9051 |
| rs546225825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031362 | TCTGAGCCGGTCAAC[A/G]AGCACCTGGTCCTCT | 9051 |
| rs546291000 | snp | A/T | 0.00141543 | 0.0265652 | utr-variant-5-prime, splice-acceptor-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995403 | CTTTTTCCTCCCCTC[A/T]GAAGCTCCTCTCTGG | 9051 |
| rs546356100 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021507 | AACATGGTGAAACCC[A/C/T]GTCTCTATCAACAAT | 9051 |
| rs546403078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001520 | GCCAGTGGCTGAGGA[A/G]TGGCCCTGGTGCACT | 9051 |
| rs546404749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013617 | CTCCCGTTGCACCCA[A/G]TAGTCTGCTCCACTC | 9051 |
| rs546651075 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004011 | CATGTTATACTCCAC[A/C]ATTAGAGAATCATTC | 9051 |
| rs546729048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019538 | GATGTGGCATGAGCC[A/G]TGTGTGAGGCCAGAA | 9051 |
| rs546757722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031440 | TTTGCCCCCAGAACC[A/C]CAAGACAGGAGCTCA | 9051 |
| rs546806361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002420 | TTCTGCAAGTCAATA[C/T]AGAGTACCTTTGTCA | 9051 |
| rs546866313 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024100 | ACCTGTGCTGGCAGA[A/G]TTGTGAGCAGTTCTG | 9051 |
| rs546970289 | in-del | -/CTGTGGTCCT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029354 | TTCCATGGAGCTAGC[-/CTGTGGTCCT]CTGTGGTCCTCTGTG | 9051 |
| rs547032830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015585 | CCTGGGGGTGATGCT[A/G]ATGCTGGGTCTTGGG | 9051 |
| rs547034292 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030968 | GAAGGGAGGCTGGGG[C/T]AGGGACCCCCTGGGC | 9051 |
| rs547082941 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002056 | TGAATCCCAGCTACT[A/T]ACATCATCCCCTGAG | 9051 |
| rs547088375 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036050 | TTCACTCATCTTCGA[A/G]CATCCTCTCCTCCTC | 9051 |
| rs547169709 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033714 | GAGAGGCTGATGCAG[C/T]TCCCGGCCCTTCCCA | 9051 |
| rs547251614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026747 | CAGGGGGTCCCCAGA[A/G]GCCAGCCCAGGCTTG | 9051 |
| rs547357649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029390 | AGGTTGCTTGTGGAT[A/G]ATGGCATCTGCCCAT | 9051 |
| rs547371069 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994545 | TCCCATTCACTGAGC[C/T]GGAAGCCTCCATCTT | 9051 |
| rs547376518 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017929 | CCGGCCCTGTCAGCT[G/T]GGTGGGGCTCACTTA | 9051 |
| rs547437295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018356 | CAAACTCTGTCAGAA[A/C]ACGCCCTGCTTTAAA | 9051 |
| rs547439197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011807 | ACTGTAGTGATGGGC[C/G]CTCCTCACCTGTCAA | 9051 |
| rs547547442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012402 | ATCCATCCACCCACC[C/T]ACCCATCTACCCATC | 9051 |
| rs547554152 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024934 | GAGAGAGGGCTGTGA[A/G]TGTGGGAGAGGAGTT | 9051 |
| rs547616901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019089 | TGGGCTTAGCTGAGG[C/T]CTGGTTAGAGGGCAG | 9051 |
| rs547653746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023029 | CACCTGGCAGTGCTG[C/T]ACGTTCAGGCAGGCT | 9051 |
| rs547672287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006288 | AGAAAGTCTATTTAA[A/G]ACCTTTGCCCACTTT | 9051 |
| rs547704597 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998698 | CTGAAAAGCAGCTGT[A/C]GTGGCACAGAAGTAG | 9051 |
| rs547779768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030348 | GTGGGTGGCCCTGAC[A/G]GGCATTCAGATGAGG | 9051 |
| rs548043559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000045 | GTATGGGGACAATAG[A/G]CCTGAACTTTCCCCT | 9051 |
| rs548056531 | snp | A/G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014912 | ATGGCCACACACCAT[A/G/T]GACGGCGAGGGCTGG | 9051 |
| rs548058165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023971 | TCACCACACAGCCAC[C/T]CCTCTCCTTCTTCCT | 9051 |
| rs548068922 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001065 | CACTGTTCATGGCTG[C/T]ACAGTTCTCTAGCTT | 9051 |
| rs548114960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029962 | GTCCTTCACTTGATG[C/T]CCGAATCCTACCAAC | 9051 |
| rs548143783 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993221 | CAAAGCCGAATTGGC[C/T]GTCTGGTCGCCCAGC | 9051 |
| rs548144725 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019120 | GCCGTCAGGGAAGTG[A/G]CTCTGATGAAGCGGG | 9051 |
| rs548153404 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034928 | GTAAAGTAGCCCAGC[A/C/G]CTGTCCCGGAACTCC | 9051 |
| rs548186174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013186 | TGCTGCTACGTCTTG[C/T]TTCCCCACCTGTGGC | 9051 |
| rs548225976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006360 | TATATTTTCTAGATA[C/T]TCATCCTTTATCAGA | 9051 |
| rs548296238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999645 | TACTAGGTGGTCCAC[A/G]CTGGACCCCTGAGCT | 9051 |
| rs548506694 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002312 | GTTCTTGCTTCTACT[C/T]TAATTTGTGTAGGAT | 9051 |
| rs548524554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035059 | GGCTTTGTGTGGCAG[C/T]GCACCCCCCACCCCT | 9051 |
| rs548824408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035380 | CATCCATGCCTGGAG[A/G]CTAGGGGCAGTCCCA | 9051 |
| rs548828496 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995138 | CACAAACCTTCCTGC[A/G]CAGGCCTCGGGCTGC | 9051 |
| rs548834548 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027312 | CCCAGACCTCGGCAC[A/G]GGGGCCCAGTGGCCA | 9051 |
| rs548847316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022818 | ACCTGGGGCAGGAAG[G/T]CCTGCAGCCCAGGGG | 9051 |
| rs548871461 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027045 | ACAGGATGGTGCACA[C/T]GTGCCTACGCTCCCC | 9051 |
| rs548887263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030433 | GAGGCATCCAGGATG[C/G]GACCTGCTGGAGTAC | 9051 |
| rs548900780 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030712 | CACTCGTTTATTCAG[C/T]CTCCTGCTCACAGGC | 9051 |
| rs548956282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005330 | GGCAGAGGTTGCAGT[A/G]AGCCAAGATTGTGCC | 9051 |
| rs549042799 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022151 | TTTTTTTCATGGTCT[C/G]TCTTCCTCTGAACTC | 9051 |
| rs549104722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016243 | AGGTGGTTCCCAGTT[C/T]TCAGGGCGGGGGGGT | 9051 |
| rs549108440 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999023 | TACCAGCTGTCTGAG[C/T]GGAGAGGGCACTGGC | 9051 |
| rs549161966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997145 | CGCAGCAGAAGCAAG[A/C]AGCCAGCCCCTGTGG | 9051 |
| rs549169658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033730 | TCCCGGCCCTTCCCA[A/G]GGACCAGCTCATTCC | 9051 |
| rs549182466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036749 | GTGCCCTGGGCTTGG[A/G]GTATGATGAGCACCC | 9051 |
| rs549289076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032186 | CAAAGACCCCGAGCC[A/G]CGCACAATGGCCTGT | 9051 |
| rs549291709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004462 | ACGGGAAACAGCCAC[A/G]CTGGGGAGGAAGTCA | 9051 |
| rs549395580 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012398 | ATCCATCCATCCACC[C/T]ACCCACCCATCTACC | 9051 |
| rs549687188 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037307 | CCTGTCGTCTCCCAG[A/G]GAATAAAGGAGTGCG | 9051 |
| rs549689881 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029249 | CCCAAGTCCCAGCCA[-/G]GGGGCTCAGCAGTAG | 9051 |
| rs549757339 | snp | A/C | 0 | 0 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76999521 | TGACCTCAGATGATC[A/C]ACCCGCCTCAGCCTT | 9051 |
| rs549757695 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022892 | TACCCCAGACAGAGG[G/T]AGCACCAGTATCTAT | 9051 |
| rs549865461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007007 | CCTGAGTTTGCCCAG[C/T]CTGGACTGGCCACGA | 9051 |
| rs549910854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024110 | GCAGAGTTGTGAGCA[A/G]TTCTGACGTCTGGAT | 9051 |
| rs549920488 | snp | C/T | 8.34237e-05 | 0.00645793 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032479 | CTCAAGTGCCAGGAC[C/T]GGGCTGGGGTAGCTC | 9051 |
| rs549927125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032191 | ACCCCGAGCCGCGCA[C/T]AATGGCCTGTGAGGA | 9051 |
| rs549937061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017878 | GCTGATGTGTGTCCT[A/G]TCCTGTGAGCTCTCC | 9051 |
| rs549993934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997787 | CTGAAGCTTCATTTG[C/T]AGACAAATCTGTAAA | 9051 |
| rs550031268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999080 | AGCCCAGAGAAGGAA[A/G]GGTCCTCCCCCTGCC | 9051 |
| rs550076425 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026749 | GGGGGTCCCCAGAAG[A/C]CAGCCCAGGCTTGAG | 9051 |
| rs550130032 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993249 | AGCCTGGGGACCTGC[A/C]ACAGGTAAGGGTGGA | 9051 |
| rs550138072 | in-del | -/G | 0.00597604 | 0.0543351 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017531 | CCTGGATCTCCGTGA[-/G]GGGGGGTTTCCTGAG | 9051 |
| rs550153725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002334 | GTGTAGGATGAAAGG[A/G]TGCTTCCCTACATGT | 9051 |
| rs550297746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995823 | GCGTCCTCCTCTCTG[C/T]TGCCCCGTGTGTTTT | 9051 |
| rs550315228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007889 | GTGAGCCACCGCGCC[C/T]GACTGGCAATAGAAC | 9051 |
| rs550378746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008478 | GCAGTGGCACCGTGT[C/T]GGCTCACTGCAACCT | 9051 |
| rs550428234 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993855 | TTTACACTATTAATT[A/G]TCTTCAGCTGCAAGT | 9051 |
| rs550432786 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017810 | TGAGTGAATTTCAGG[C/G]CTGGCTGTCATCAGG | 9051 |
| rs550450801 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037674 | AGGCCAGGGCAAGTG[C/T]GTGGGCAAAGGTGAG | 9051 |
| rs550465892 | in-del | -/GCCCCCCACATGCCACCTTGAATTGCAGGGCT | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034446 | CCTCATGTGGGAAAG[lengthTooLong]GCCCCCCACATGCCA | 9051 |
| rs550537172 | in-del | -/CAGGCCCCTCCCTG | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036976 | TGGGTGGGGGAACGC[-/CAGGCCCCTCCCTG]CAGGCCCTTCCCTGC | 9051 |
| rs550554582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996503 | CAACCCCGAAGAGGA[C/T]GCTCTGGCCCTCGGC | 9051 |
| rs550702537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014382 | GAAACAGGCTGAGAA[A/G]GGCCAGGGTCACGGG | 9051 |
| rs550715756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010157 | TCGGCCTCCTTCCTC[A/G]CCCACTGCTGGATCC | 9051 |
| rs550722673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021202 | TGACCTCAAACCAGC[C/T]GGGAGCCACCCTCAG | 9051 |
| rs550724294 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001502 | GCTTTGAGGGCCAAG[A/G]AGGCCAGTGGCTGAG | 9051 |
| rs550724823 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027128 | TTGTGCTGTGTGTGT[C/G]TGAGTGCCTGTGCCT | 9051 |
| rs550750763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036785 | CCCTGACATGCTCCA[G/T]TCACTGCGTCTCCAG | 9051 |
| rs551011442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003262 | TTTGGGTGGAAACCA[A/G]GACTGCCTCTGCTTC | 9051 |
| rs551056611 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021527 | CTATCAACAATATAA[A/G]AATTAGTTGGGCATG | 9051 |
| rs551123591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003664 | CCGTCTCAAAAAAAA[A/G]AAAAGAAGAAGAAGG | 9051 |
| rs551158769 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999300 | TTTTTTTTTTTTGAG[-/A]AAGAATCTTACTCTG | 9051 |
| rs551234855 | snp | C/G | 9.94283e-05 | 0.00705012 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027947 | GGGCCGCGGCCTTCC[C/G]TCGAGGAGCAGCGCA | 9051 |
| rs551251523 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008197 | GCACAGGGTGTGGGT[A/G]GGGTGTTTGGGGATA | 9051 |
| rs551296934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015620 | AGACCCACATGACTG[A/G]TTAAGTTACAGGATG | 9051 |
| rs551327464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032033 | TCACTCTCCTCTGAG[A/T]TTCCTCATCTATCCA | 9051 |
| rs551355790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002958 | ACAAACGGCACTCAA[A/G]GTGGGAGGTACGGCA | 9051 |
| rs551392704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031617 | AGAAGCTGGAGGACC[A/G]TGGCTGCTCTGCTCT | 9051 |
| rs551395257 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027149 | GCCTGTGCCTCGCTG[C/G]TCTCCCAGCTGGCAC | 9051 |
| rs551466220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033217 | TCTGGGGAGGCCCCT[A/G]TGCTGGCTTCCTTGT | 9051 |
| rs551496571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004331 | TTCCACTGGTGTTGA[C/T]AGGCCACCCACCATT | 9051 |
| rs551624273 | in-del | -/G | 0.00120096 | 0.0244753 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017531 | CTGGATCTCCGTGAG[-/G]GGGGGGTTTCCTGAG | 9051 |
| rs551658974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036389 | TGTCCTTCGTGGCCA[A/T]GGGTGTGGAAAACTG | 9051 |
| rs551693712 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001329 | GCAGTCACTTTGGGA[-/T]TCCCCCATAGTCCTC | 9051 |
| rs551742974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036690 | GTGGCTAGCTGGGGC[C/T]GGGGACCGCAAAGGG | 9051 |
| rs551810833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035098 | GGGAAGCTGCTAGGG[C/T]AAGCTAGAGCAGGGG | 9051 |
| rs551878618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998527 | TTAATGAGCTTGGTC[A/T]TGGGGTCTTTTAGCC | 9051 |
| rs551894330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035410 | AGCCCTGGCAGAGCG[C/T]GTGCAGCTCTGAGAC | 9051 |
| rs551912798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024781 | GCCCACCTCTCAACT[C/G]CTGCGCCCTGCCCTG | 9051 |
| rs551977996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019015 | ACACTCTGTGGCTCC[A/G]TTTCCTCATCAGTGA | 9051 |
| rs551995481 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012700 | TGTGCCTCTGTTTCC[A/G]TATCTATACAATGGG | 9051 |
| rs552088349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010295 | AGTAACAGCACAGTA[C/G]TAACTTGACGGGGTT | 9051 |
| rs552123256 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014601 | GGCTTGCTTCAGGCC[C/T]TGGTGTCTGTGGTCT | 9051 |
| rs552207727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000267 | ACTCAGCCACTGGTG[C/T]CTTTTCCCTTCCCAG | 9051 |
| rs552224543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013234 | CAGTCATCTTCAGGT[A/G]TAACCCAATCCAGTC | 9051 |
| rs552273004 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76994766 | GGCAGGACCTGGTTT[C/G]GGTCCCAGAGCAGCC | 9051 |
| rs552311493 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034964 | ACAGGGTGGCTGAGC[C/T]GGCCTGATCACCGTG | 9051 |
| rs552324989 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020760 | CCTTGCCTTACTGTC[A/C]GAGTCTTGGCTTAGA | 9051 |
| rs552373075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012662 | GGAAGGAGCCTGGTT[A/G]CTACCCATTGACTTA | 9051 |
| rs552426974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008506 | CCTCCGTCTCCTGGG[C/T]TCAAGCAATTATCCT | 9051 |
| rs552576989 | snp | A/G | 0.000399281 | 0.0141238 | splice-donor-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030582 | CGGACCACCTGTGAG[A/G]TGAGTGGCCCACGTG | 9051 |
| rs552732765 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007192 | CCCCACCTGCTCTCA[A/C]TCTTCTTCAAGGAGG | 9051 |
| rs552764913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007291 | AATTAATGTCTGTCC[C/T]GGCCTCAGCTTGCCT | 9051 |
| rs552786735 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995315 | CTGGACACCAGGGCC[C/T]GCCCTCCCATCACTG | 9051 |
| rs552843898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006581 | TTTGTAGCTTTAGGT[C/T]TTACATCTAGGTGTT | 9051 |
| rs552845129 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018985 | CAGCTGTCTGACCAT[-/G]GGCTGGCTGCTGACA | 9051 |
| rs552848520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995691 | AGGTGATGGGATGCG[A/G]CTCCGAGAGGGGAGC | 9051 |
| rs552879338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026157 | CTGCATGGAAGTGAA[C/G]TCCCCATCATGGGAG | 9051 |
| rs552884144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035157 | CACGAGGCCTCAGTG[C/T]GGAGGTCCTAGAACC | 9051 |
| rs552907066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999756 | GAATAACTGGGTCAG[A/G]CAAGGAGTGCTCTGA | 9051 |
| rs552948484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019776 | AGGCTGGGCACAGAG[A/G]AGGGCTCAGGACATG | 9051 |
| rs553036923 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025743 | GCACTCCAGGCTTTG[C/G]GGCTTGAGGGTGATC | 9051 |
| rs553043890 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001268 | TTCCAGGGAAGGAGG[A/C]ATTTCTGGGTGAAAG | 9051 |
| rs553114549 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998331 | GAACACGGGGCGGAG[A/G]AGGGGAGCCAGCCCT | 9051 |
| rs553226091 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036429 | TGAGTCTTGCTATCG[G/T]GCCAGGATTGATTTT | 9051 |
| rs553328754 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994231 | CTGAGCCGGCAGGGC[A/G]TGGCGTCTCAGGGCT | 9051 |
| rs553345339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001898 | GGGATGAGGCTGAGC[A/G]GCTGTGAACGTTTTC | 9051 |
| rs553354723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008559 | GGATTACAGGTGCCC[A/G]CCACCACACCCGGCT | 9051 |
| rs553397057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008495 | GCTCACTGCAACCTC[C/T]GTCTCCTGGGCTCAA | 9051 |
| rs553410132 | in-del | -/C | 0.0422008 | 0.138995 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012983 | GGGGAACCTGAAAGA[-/C]CCCCCCTCTGCCTCC | 9051 |
| rs553431399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036076 | TCCTCAGGAGGGCAC[A/G]TGTGCCCGAGTGTGT | 9051 |
| rs553459885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996161 | TTCCCCTCACCCAGC[C/G]CCTTGTCCCTTGCAG | 9051 |
| rs553471765 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005552 | TTTAACAATTTTTAA[C/G]TATATGATTCAGAGG | 9051 |
| rs553472557 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027690 | TTCCATTGTGAGGGT[A/C]ACTGTGAAGCAGCAG | 9051 |
| rs553498924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019809 | GAGGAGTGAATGGAC[A/G]TATGCAGGGAGGTGT | 9051 |
| rs553621132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998827 | GATTTTAGCTGCAGC[C/T]GAGTGTTCAGATGCA | 9051 |
| rs553652664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022390 | GAATTTCAGACTGAG[C/G]TTCCTGAGAGCCGAG | 9051 |
| rs553718554 | snp | A/C/T | 0.000504778 | 0.0158794 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018170 | ACTTCACAGCCCACA[A/C/T]GGGCTACGAGGTGCT | 9051 |
| rs553746004 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014468 | GAGTACCCTCTCTGA[A/C]CTGTGGCCTACACTA | 9051 |
| rs553762507 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011243 | GCTGAGGGCAGGTAC[C/G]ACACTCATGCACAGT | 9051 |
| rs553825046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012169 | CATCCACCCACCCAC[A/C]CACCCACCCATTCAC | 9051 |
| rs553889803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012851 | CATGGGGCACCTCAG[A/G]AAGCAGCCGTCATAA | 9051 |
| rs553944152 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037702 | GAGGTTGGGGGTACA[A/C]CCAGGAATATTCGGA | 9051 |
| rs553957498 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993356 | CCAGTTGCTCCAGCC[C/T]GTCACCAGCATGGCC | 9051 |
| rs554080461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012628 | GAGTCCCACTGTGGG[A/G]TACTGACTGTAGGGC | 9051 |
| rs554104920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024243 | CTGATGCCGCTGGTC[C/T]GTGGACCTCACTTTG | 9051 |
| rs554148349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010576 | GGCAGCTGAGTCTGA[A/G]GGGCGTGTCTCCATC | 9051 |
| rs554154559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017283 | CTTCTCACACCCAGC[C/T]TCCCACACCAGCAGC | 9051 |
| rs554161203 | snp | A/G | 0.000633023 | 0.0177795 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77029561 | GCAGTGCAAGGACTC[A/G]GCCACCGAGGCAGGT | 9051 |
| rs554173226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023656 | TCCGGTTTTGGACAC[A/G]CTGAATTTGAGGTAT | 9051 |
| rs554179125 | in-del | -/CAGGCACCTCCT | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032736 | CTCATGGGAGCAAGA[-/CAGGCACCTCCT]CAGGCACCAGGATGG | 9051 |
| rs554250364 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031851 | GTGTTTCCTGCCTGA[C/T]GCTCCTGTCCGGGGC | 9051 |
| rs554283921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999244 | GAATGTCTCCATGGT[C/T]CATCTCCCTTCCTGA | 9051 |
| rs554318659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033920 | TTGTGAGACAGGCTT[C/T]CCTGTGCCTGGTGAG | 9051 |
| rs554343807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999201 | GTACTGGCTGAGGAC[A/G]TGTTCATAGAATAAA | 9051 |
| rs554349409 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016946 | GACCCTGGAGTGTGC[A/G]TGACCTTGGAGACTG | 9051 |
| rs554408944 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037269 | GGGCCCAGAACCAAG[C/T]GTCCCCCAGCCCCGA | 9051 |
| rs554428114 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033832 | GAGGGCACACACACA[A/C]CCTCTTTGAGAATCT | 9051 |
| rs554509151 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995147 | TCCTGCGCAGGCCTC[A/G]GGCTGCCTGCCTGCC | 9051 |
| rs554509883 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011166 | CATTAGAGAGAGTCA[C/T]CTCTCTTGTCTTCAC | 9051 |
| rs554510662 | in-del | -/GTT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037463 | GAGGCTTCAGCTATA[-/GTT]GTTGGAGAAGAGGCC | 9051 |
| rs554526347 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033609 | GTCTGTGGGTTTCAC[A/G]TGGTGCCTGTGCCCC | 9051 |
| rs554561176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005858 | ACTATTCCATTCTAC[A/G]TATATACTTTATTTT | 9051 |
| rs554623274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006661 | CTTAATTCTTTTGCA[C/T]GTGGATATCCAGTTT | 9051 |
| rs554657577 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999688 | AACATCTAATCAGAT[C/G]AATGAAACTGTCTTG | 9051 |
| rs554687342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034411 | CATGTGTGTGCACTC[C/T]TGGGGCCTTGGCCCT | 9051 |
| rs554716820 | snp | C/T | 0.000176694 | 0.00939765 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029599 | CCTGGCTGCCCCGTC[C/T]GACCAGGGCGGAGGC | 9051 |
| rs554882846 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011323 | TCCCTGGAAGCTCAC[A/G]GGGCTCTGATGGGGT | 9051 |
| rs554913901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019119 | GGCCGTCAGGGAAGT[C/G]GCTCTGATGAAGCGG | 9051 |
| rs555010436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018641 | CTGGGCAGAACCAGG[A/G]TAGGTCTGGATTGCT | 9051 |
| rs555136135 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993960 | TCTGGGGGCAGTCCC[A/C]TTGCTCTGCAATCCT | 9051 |
| rs555145672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015805 | GCAGCCCCTGGAGAG[G/T]CAGGCACTTCCTCGG | 9051 |
| rs555175503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030096 | CTACTCCCTCGGCTG[A/G]GGGACAGGTGACCTC | 9051 |
| rs555260265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996646 | CCACTTGGGGCCTGT[G/T]GCCAGCGTGTGAGTG | 9051 |
| rs555335734 | in-del | -/AAAG | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003666 | GTCTCAAAAAAAAAA[-/AAAG]AAGAAGAAGGAAGCG | 9051 |
| rs555368425 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028287 | GCGAGGGGCGTGCCC[C/T]CGCCGAAGAGCACAG | 9051 |
| rs555404648 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017670 | CCAGCCAGACAGCCT[-/G]GGGTTCAAGGCCAGG | 9051 |
| rs555495834 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003422 | TTCTTGGGAGGCCGA[A/G]GCGGGTGGATCATCT | 9051 |
| rs555626407 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026597 | CAGCCCAAGCCATGC[G/T]CCCCTCAGTCTCCAC | 9051 |
| rs555636185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021378 | CAGGGATCCCCACCA[A/G]CGCTTTCAGTGCATT | 9051 |
| rs555653648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032712 | TTGATGGTACCTACG[C/G]TGGGGTCTCTCATGG | 9051 |
| rs555658119 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027975 | GCAGGTCTCAGGGTG[C/T]GATCCTGGGCTGTGG | 9051 |
| rs555691324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026940 | AAGTGGCCAGGGCCC[C/T]GCAGGCAGAGCGCTG | 9051 |
| rs555705592 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000632 | ACTGCTAATATTATG[C/T]TGTGTTTGCATAAGA | 9051 |
| rs555820675 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022520 | ACACAGTAGAGGTGC[C/T]CAGGGAGATCTTGAC | 9051 |
| rs555847538 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016459 | TGGAAGCCTGGTCCA[A/T]GCTAACCCAGTGATG | 9051 |
| rs555874735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003865 | CCACCTCCTGCTCAC[C/T]ACAGTGGAGTAGCAG | 9051 |
| rs555940090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036863 | AACTATGATGACAAA[C/T]TGAGGGGGATGGGAG | 9051 |
| rs555944050 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997561 | TATTCAGATGAGGAA[A/T]TTGAGGCACGGAGAT | 9051 |
| rs556220122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017536 | ATCTCCGTGAGGGGG[A/G]GTTTCCTGAGCCCAC | 9051 |
| rs556287550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018006 | TGTAAAGCCAGGTCT[G/T]GAGTCCCAAGAGCTT | 9051 |
| rs556322755 | snp | C/T | 4.95712e-05 | 0.00497827 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037173 | CTACCTGGAGAAGCT[C/T]TGAGGAAGGGCCAGG | 9051 |
| rs556332485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998005 | CACTCTGGGAGGCCA[A/C]GGTGGATGGATCACT | 9051 |
| rs556346366 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998699 | TGAAAAGCAGCTGTA[C/G]TGGCACAGAAGTAGT | 9051 |
| rs556397189 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032177 | CCTCAGGATCAAAGA[A/C]CCCGAGCCGCGCACA | 9051 |
| rs556470201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015888 | GCCCAAAGCTCTGAG[C/T]GGGGGACTGGGCGGG | 9051 |
| rs556483638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021906 | TATTGCTCATCCTGC[A/G]TCAGGTAAGGTGCTG | 9051 |
| rs556511522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025835 | AGCCCCATGGAAGGT[C/T]CTTCCTGTCGAGCTG | 9051 |
| rs556579932 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014975 | GGAAGAGACTGTGCC[C/T]GCTCCCCACCTGGCA | 9051 |
| rs556586494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029016 | CACAGTAAGTGACTT[A/G]TCTAAGGTCTCAGAG | 9051 |
| rs556625090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026515 | CCATACCACTTCCCA[G/T]CTCTGTGCCTCAGTT | 9051 |
| rs556668291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011369 | GCCTGTGGGCCTCCC[A/C]GCACAGTGGAGCCCA | 9051 |
| rs556684604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020756 | CTTGCCTTGCCTTAC[C/T]GTCAGAGTCTTGGCT | 9051 |
| rs556692485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000570 | AAGGAAAGTGGGGAA[A/G]TGGAGAAAAATAGGA | 9051 |
| rs556753775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001099 | AATTTGGTGACCATG[A/C]TGTGATTTTTTTTGC | 9051 |
| rs556765694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020033 | CCCCAGCAGGGCACA[A/G]TGGGAGCCAGGCTGG | 9051 |
| rs556776982 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996624 | CTTCCTTCCCTTCCG[A/G]CCGGCTCCACTTGGG | 9051 |
| rs556778255 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995800 | ACGCAAGTGGACTCC[A/G]TGAATGAGCGTCCTC | 9051 |
| rs556813421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028466 | CCCTCGCCAGGGAAA[A/T]AGGGAGGCTGGGCTA | 9051 |
| rs556826963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014158 | GTTATATCCCAGCTG[C/T]ACCCGGCAGGTCCCT | 9051 |
| rs556840256 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029188 | TGAGGCCCAGAGAGG[G/T]AAGTGGCCTGAGGGT | 9051 |
| rs556892268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035188 | CCCAAAGGGCCATGG[G/T]AGTCTTCCAATGAAG | 9051 |
| rs556896344 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994903 | GCTGGACTGGCTGGC[A/G]GGTGACACACCTGGG | 9051 |
| rs556929070 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011512 | CTCATTTCTAATCTC[A/G]AGGTCCTGTCAGCCC | 9051 |
| rs557073616 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996360 | ACCCCTGGTCATCTC[A/C]GCACTTTTCCAGCTG | 9051 |
| rs557081126 | in-del | -/CCTCCAGCGC | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030163 | TGGGACTCCACCCCT[-/CCTCCAGCGC]CCTCTCAGCTGCCTT | 9051 |
| rs557096525 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017836 | TCAGGGGGACTTAAG[C/G]GTGGCTCTTCCCATC | 9051 |
| rs557172402 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, synonymous-codon | PSTPIP1 | GRCh38.p7 | 15:77035527 | TCTGGACTGCTGCAC[A/G]GAAGTCCCAAGACCA | 9051 |
| rs557184216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032211 | GCCTGTGAGGAGGCC[A/G]GTGGGTGGGGGCCGC | 9051 |
| rs557231824 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030905 | AGGGCTCAGGACTCC[C/G]GTCCGAGGTCCCTCT | 9051 |
| rs557253922 | snp | C/T | 0.000112822 | 0.00750989 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995447 | TCTGAGTGTTGCAGA[C/T]GGCGCCGGCCGGGAA | 9051 |
| rs557341423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036467 | CCATAGGGTGAGGAT[A/G]AACCAAGGCAGCCAC | 9051 |
| rs557388010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002590 | GGGGACCAAGAACTT[C/T]GTTCATCTGTGCCCA | 9051 |
| rs557398563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036218 | GGCCTGTGTCTGCCC[A/G]GGCCTGTACACAGCA | 9051 |
| rs557399618 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996670 | GTGAGTGTTCTGCTT[C/T]CTCTGCTCTGACTGT | 9051 |
| rs557402982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009145 | AAGCAAGGATAAGGA[C/G]CCCCACGTGCCATCC | 9051 |
| rs557414835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021311 | AACTCAGCAAACATC[A/C]GTGGGGCAGTGGCAA | 9051 |
| rs557416491 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014700 | CTCCACTCAAGCCGT[G/T]GGGGTGTGGAGGGCC | 9051 |
| rs557425646 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031762 | GAGGGCCCCCAGCCA[A/G]GGTCCCTGAGCTCTG | 9051 |
| rs557501782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026961 | CAGAGCGCTGTGTTG[C/T]AGTGTGTGCCATGTG | 9051 |
| rs557515423 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002982 | TACGGCATGGGCAAA[G/T]GTGTGGAAGGGGGTT | 9051 |
| rs557528832 | snp | C/G/T | 0.000828821 | 0.0203409 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995464 | GCGCCGGCCGGGAAG[C/G/T]GGGGCCTGGGCCAGC | 9051 |
| rs557539109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996034 | TCAGTCTCTCCATCT[A/G]TATAATGGTGATAAA | 9051 |
| rs557614898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008740 | CTACCTCTGTGTAGG[C/G]TGAGAGTAAAACGTT | 9051 |
| rs557663802 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001783 | AGCATTTATACTGGC[G/T]CAGGCTTGTAGTATT | 9051 |
| rs557720122 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002082 | CTGAGGAGCAGCAAT[G/T]CTGCCATTTGCTGAG | 9051 |
| rs557759616 | snp | C/T | 7.01434e-05 | 0.00592172 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77032303 | CCTGCCCCAGCTCTA[C/T]GAGGAAGTGCGGCTG | 9051 |
| rs557975957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028248 | GAGGGGCTCCTAAGA[C/G]GGCGCGGCGTGGCGA | 9051 |
| rs558025594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036522 | GCTCCCTGCTTGAGG[A/G]GAAGAATGCATAGCC | 9051 |
| rs558026848 | snp | A/T | 0.000490474 | 0.0156524 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031151 | TGCAGCCGCCTCCTC[A/T]CTGCTCACCTCCCTC | 9051 |
| rs558046398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031809 | AGCACACGGCTCTCC[C/T]GGGCAGCCCTGGCCC | 9051 |
| rs558062415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036809 | TCTCCAGAATGGGAG[A/G]GGGGAGGTGAGGCTG | 9051 |
| rs558091886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009945 | GACCACTGGTGCCCC[C/T]GGCTGGTCACTCACA | 9051 |
| rs558204033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003327 | GCCCACACCAGGACT[C/G]TCCTCTGGGTTGGCT | 9051 |
| rs558290697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009302 | CTTCAAGGAAGGGCA[C/T]GGGCATAGGAGTGGA | 9051 |
| rs558315961 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037388 | AGTGTCCGAGTGCTC[A/G]GTTCAGAGGAGGCAA | 9051 |
| rs558352326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002640 | CTGCTCAGGTGTTAG[A/G]AGATTGCAGAGGTTT | 9051 |
| rs558365336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030167 | ACTCCACCCCTCCTC[C/T]AGCGCCCTCTCAGCT | 9051 |
| rs558378599 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011032 | AGAGTGAAGGAGGGG[A/T]AGCAGGCGGGGAACT | 9051 |
| rs558421403 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037778 | GGCCATGGTGGGAGC[C/T]CAGGAAGACAGGCTT | 9051 |
| rs558424208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012089 | CTCTGGGTAAGCAAC[C/T]GCCTTGTTTACTGAG | 9051 |
| rs558493092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006014 | CTAGGAGTGGAATTG[C/T]TGGATCATATGGTAA | 9051 |
| rs558525924 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996790 | GCCCAGAGAAGCCAA[A/T]GGAGGCAGAGCTGCC | 9051 |
| rs558583629 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993474 | GGAGGATTTGCCCAG[A/G]TAAGGAAGATCAAGG | 9051 |
| rs558627384 | snp | A/G | 3.51043e-05 | 0.00418938 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030527 | CAGGCAGAGCATTGC[A/G]CAGCTGGAGAAGGTC | 9051 |
| rs558641819 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007488 | GTGGTGCACACCTGT[A/G]GTCCCAGCTACCTGG | 9051 |
| rs558691808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024431 | CCCCTCCACCCAGGG[A/C]TGTCCGGTGGGCGTC | 9051 |
| rs558803478 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013618 | TCCCGTTGCACCCAA[C/T]AGTCTGCTCCACTCA | 9051 |
| rs558843916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034069 | ATGTCCTGCAGGGCC[A/G]AGGGAGGCCTGGCTG | 9051 |
| rs558844019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006469 | GAATTCAATGTGTCT[A/G]CTCTTTGTTTTGTTG | 9051 |
| rs558898543 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015277 | TGTAGGTATATGGCT[C/T]TGGGGACAGGTTGAC | 9051 |
| rs558935247 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007998 | CCAGCTCTGAGCCCA[C/T]TCTCCTAGGCATCAG | 9051 |
| rs558948357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013840 | GTCCTCTGATAGATG[C/T]TGTATTCTGGAGTGC | 9051 |
| rs559079843 | snp | C/T | 1.66402e-05 | 0.00288441 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025296 | CAGCTCCCTGAGGGC[C/T]TCCTTTGACTCCTTG | 9051 |
| rs559096623 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033716 | GAGGCTGATGCAGTT[C/G]CCGGCCCTTCCCAAG | 9051 |
| rs559111574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018364 | GTCAGAACACGCCCT[G/T]CTTTAAAAAACTCTT | 9051 |
| rs559126311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035619 | TGGGGGGGAGGAGAG[A/G]TCTCCCACATGGCAC | 9051 |
| rs559133968 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034209 | AGAGGTGTGGGGGCA[C/T]GCAGCACAATGGCTC | 9051 |
| rs559160570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029438 | TCCCCCCAGGGTGGC[C/T]GGGGAAGCTTGACAG | 9051 |
| rs559174929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029712 | CTCATTCCAGATATG[C/T]GCCGTCAAAGTAAAC | 9051 |
| rs559236782 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030239 | GGGCGCCCAGAGATG[A/C]CCAGAGGCCAATACT | 9051 |
| rs559276121 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019163 | CACAGGTCTCTGCAC[A/G/T]CAGACTGCTGGGGTG | 9051 |
| rs559297012 | snp | C/T | 0.000162061 | 0.00900025 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015959 | TCACAGCCTGCAGGG[C/T]CTCTCGCTGCTTTCT | 9051 |
| rs559327368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77024531 | AATACTGGATGCCCA[A/G]GTGAACGTGAATTTC | 9051 |
| rs559408829 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996262 | CTTAAATCAAGTCAT[C/T]TCCCCCATGAAATAA | 9051 |
| rs559452754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999388 | GGGTCAGGTGATTCT[C/T]CTGTCTCAGCCTCCC | 9051 |
| rs559460861 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035004 | GGAGGAGGGCTGGCT[C/T]GGCCCAGGCAGTGGA | 9051 |
| rs559516820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023208 | ATGAGGAGGAGAGCC[A/T]GGCATTGCCCCTGTC | 9051 |
| rs559523988 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036520 | CTGCTCCCTGCTTGA[A/G]GGGAAGAATGCATAG | 9051 |
| rs559651377 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995090 | CTCCACTTCCTGTGG[A/G]CGAGGGCCCTGTGCC | 9051 |
| rs559657451 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023344 | AATGGAGATGGGCAC[A/G]TGCAAAGGCCCTGAG | 9051 |
| rs559758018 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035243 | CCTCCCAAGGGCCCT[A/G]CAGGGAGCAGGTGCT | 9051 |
| rs559775810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000836 | GTGAGCCACCATGCA[C/T]GGCCCTCCCTCCTTT | 9051 |
| rs559775969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000047 | ATGGGGACAATAGGC[C/T]TGAACTTTCCCCTTG | 9051 |
| rs559835773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031021 | CCTCAGGGCTGGCCC[A/G]GAGTCGGGATGGGGA | 9051 |
| rs559948810 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013464 | ACATCTCATTGCCCT[C/G]GTACTGTTGTAACTG | 9051 |
| rs560033500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000873 | CTAGTATTTTAAATT[G/T]TATTTTAAATTGTAG | 9051 |
| rs560054238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997128 | GAGCAGGGTATGGCA[C/G]CCGCAGCAGAAGCAA | 9051 |
| rs560078872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011405 | GGCATCTCTGGGACT[C/T]GGCCAGCTGGGCTGC | 9051 |
| rs560094760 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034935 | AGCCCAGCGCTGTCC[C/T]GGAACTCCTGTGAAC | 9051 |
| rs560108029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998099 | AAAAATTAGCCAGGC[A/G]TGATGGCATGCTCCT | 9051 |
| rs560140065 | snp | G/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993888 | CAAAAAACCTGACTG[G/T]GGCGCCTTACAGATT | 9051 |
| rs560145649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027966 | AGGAGCAGCGCAGGT[C/G]TCAGGGTGCGATCCT | 9051 |
| rs560214227 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003076 | CTGGATTGTGAAAGG[C/T]CTCTGCCCTAAGTGG | 9051 |
| rs560227782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003487 | GGTGAAACCCTGTCT[C/T]TACTAAAACTACAAA | 9051 |
| rs560296742 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026316 | GCTGAGCCTCTCAGG[A/G]CCTTAGTGATGAGGG | 9051 |
| rs560360445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005174 | AGATCACCTGAGGTC[A/G]GGAGTTCAAGACCAG | 9051 |
| rs560418994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017639 | CTGCACAGTGCTGAG[A/G]TGAAGGGCAGGGACC | 9051 |
| rs560485131 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006830 | ATGACACTACCGCAC[C/T]ACTTCAATTACTGTA | 9051 |
| rs560584334 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028739 | GTAGACACCCCCAGG[C/T]AAGATCTGCATCTGG | 9051 |
| rs560673758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006030 | TGGATCATATGGTAA[G/T]CCTATGTTTAACTTT | 9051 |
| rs560901290 | snp | G/T | 0.000153175 | 0.00875007 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028691 | TGGGTCGCCCAGGGC[G/T]GGGGGCAGTGGGGGA | 9051 |
| rs560905267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006168 | TAGCCACCTTAGGAG[G/T]CATGAAGTAATATCT | 9051 |
| rs560964934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029320 | CATCCTCCTGGGCTC[A/G]GTTCCTGTCTTCGTT | 9051 |
| rs560975220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023261 | GCGTGACAGACATCC[A/G]CTGGGCCAGCCCAAA | 9051 |
| rs560975548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033531 | GAGCACTATAGCCAG[C/T]TTAGGGAGCCCTCGT | 9051 |
| rs561014883 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037248 | AGCACTGTCCCCACC[G/T]TGCTAGGGCCCAGAA | 9051 |
| rs561031769 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003635 | CACTCCAGCCTGGGC[A/C]AAAGAACGAAACTCC | 9051 |
| rs561068208 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029744 | CTGTGTTCCCCCATT[C/T]GCCAGCCCTTCTTGG | 9051 |
| rs561088167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999834 | CCCGCAACCTGTATG[C/T]CTATCCAATGGCCTT | 9051 |
| rs561144576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004179 | ACACAGATGGATCGG[A/T]CTGGGCTGGGCCTGG | 9051 |
| rs561216697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997751 | GGTAAGAAAATCAGA[A/C]AAGGTGGCTAGAACA | 9051 |
| rs561315173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008904 | TTGGGCAGAGCAGGG[C/T]GATTTCCCAGACTCC | 9051 |
| rs561405744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011446 | GGCCCTGTAAGGCCC[A/G]GCAGAGGCCATCAGA | 9051 |
| rs561478916 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007980 | ATTGCCCATTGACCT[-/G]GACCAGCTCTGAGCC | 9051 |
| rs561490190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002802 | TGATGACCCACTTTG[C/T]GCTCCAGTCCCCTGG | 9051 |
| rs561523366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036763 | GGGTATGATGAGCAC[C/T]CGTGACCCCTGACAT | 9051 |
| rs561612836 | snp | A/G/T | 0.000406072 | 0.014244 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018277 | CAGGCCATGGGGAGC[A/G/T]CAGGCAGGAAGCAGG | 9051 |
| rs561638035 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014318 | TTTCACTTGCTTCTC[C/G]GGTCACCTCTAGGCG | 9051 |
| rs561650104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014721 | GTGGAGGGCCCTGGC[C/T]GGCTCACAGGCCTGG | 9051 |
| rs561652533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008443 | GAGACAGAGTCCCAC[C/T]CTGTTGACCAGGCTG | 9051 |
| rs561673184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012210 | GTCCATCCATCCATC[C/T]GTCCACCCATCTGTC | 9051 |
| rs561802269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002223 | GACGAGGGTCACCTG[G/T]GCAGGGTAGAGCAGG | 9051 |
| rs561810243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036277 | TCCACACAGGCTGGG[C/T]GCTGAGTGGTGCACA | 9051 |
| rs561824255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020974 | TGAGTAGGGGAAGCC[C/T]CTGGCCTCCCTGAGG | 9051 |
| rs561947187 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020346 | CCAGGGTCTGTACCT[A/T]TGGAAGGGGATGGTC | 9051 |
| rs561981911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031938 | TCCTCGCCTCCTTGA[A/G]GTAGAAGGGCGAGCT | 9051 |
| rs562055559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027764 | CAGGAGAGGTGCTGC[A/G]CCTCATCCCAGGGAC | 9051 |
| rs562086519 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015586 | CTGGGGGTGATGCTG[A/C]TGCTGGGTCTTGGGT | 9051 |
| rs562166955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010109 | AGTCACCCCCAAGGG[C/T]CCACGGCCTCCCTTC | 9051 |
| rs562415753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021615 | ACCTGGGAGACGGAG[G/T]TTGCAGTGAGCCCAG | 9051 |
| rs562511130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036646 | GCAGGGAAGCCAGGC[C/T]AGGAGAGTGATGGGG | 9051 |
| rs562560105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031999 | GCTGTGCTGCATTCT[C/T]GCTGTGACCTTGGGC | 9051 |
| rs562562986 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036949 | CCCTGGGAGACATGC[C/T]GCATTTACTGCTGGG | 9051 |
| rs562684818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009564 | AGTTCTCCTTGTAAA[C/T]GCCCCTTCCCTGGGC | 9051 |
| rs562711438 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026750 | GGGGTCCCCAGAAGC[A/C]AGCCCAGGCTTGAGG | 9051 |
| rs562828458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010716 | GCAATGGCTCAATCT[C/T]GGCTCACTGCAGCCT | 9051 |
| rs562839316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022133 | TCAGAGAGATTTTTA[A/T]AATTTTTTTCATGGT | 9051 |
| rs562847523 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011535 | GTCAGCCCAGGTGAA[A/C]AAAGAGTCGCTCATC | 9051 |
| rs562849866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022601 | AATGACTTTATGTGG[C/T]CCCCAGATCCTCCCC | 9051 |
| rs562890795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004262 | TGTGTTGGTTTGCTG[A/G]GGCCTGGCACACTGA | 9051 |
| rs563112630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013205 | CCCACCTGTGGCCCA[C/T]GCTGGAGCTTTCCCA | 9051 |
| rs563204466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016144 | GTCCCCTGAGAGTCC[A/G]GATTCTTGTCCTGAC | 9051 |
| rs563241284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024687 | ATTCTGGCAGCCCCC[A/G]CCCATCATTCCCTGC | 9051 |
| rs563251799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025427 | CTGGGCTGGCCCACA[C/T]GGGTGAGTTGTGGGT | 9051 |
| rs563383866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013553 | TGGTGACCCTGCCCC[C/G]CTGGAGTCCCTGACC | 9051 |
| rs563446112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018970 | CAGCTCCTCACCCCC[A/C]AGCTGTCTGACCATG | 9051 |
| rs563458003 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015710 | AGTCAGACCCATGCC[C/G]TCGAGGAAGTGGCAG | 9051 |
| rs563559411 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014428 | TCTAGTCAGTCAGAC[A/C]CTTCCCAGCCTCTCA | 9051 |
| rs563768176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026661 | TGGCAGAAATGTAGC[A/G]TGGCTGCCCGTGCCA | 9051 |
| rs563780956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021022 | GGTCTATGGGATGCT[C/T]ATTCCCTGCCCCTTG | 9051 |
| rs563888309 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029253 | AGTCCCAGCCAGGGG[A/G]CTCAGCAGTAGTTGC | 9051 |
| rs563906441 | snp | C/T | 0.000363548 | 0.0134775 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018478 | GGCGGAGGAGCGGTA[C/T]GGGAAGGAGCTGGTG | 9051 |
| rs564040947 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995681 | ATCTCCATGCAGGTG[A/T]TGGGATGCGGCTCCG | 9051 |
| rs564043381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020283 | GGGGCAGGGTCTGCC[C/T]TGACTTATCCTTTGT | 9051 |
| rs564043400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013582 | CCACTCCGTTCCCTA[A/C]AGCCTTCCACTTCCA | 9051 |
| rs564336596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025445 | GTGAGTTGTGGGTGG[C/T]TGAGGCCCATCAGAT | 9051 |
| rs564351665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027031 | AAGGACATGTGCTTA[C/T]AGGATGGTGCACACG | 9051 |
| rs564503175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021043 | CTGCCCCTTGCAGAA[C/T]GGGCAGGGGACTGGG | 9051 |
| rs564565151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031098 | TGGCCTGGTCAGCTC[C/T]GGCTGAGCTGTGAAT | 9051 |
| rs564586190 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003886 | GGAGTAGCAGACCAG[A/G]AACAGTTCCCAGGGG | 9051 |
| rs564622092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995695 | GATGGGATGCGGCTC[C/T]GAGAGGGGAGCTTTC | 9051 |
| rs564693267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996416 | AGCTCTGGCTGTGCC[C/T]AGGGCTCTGGGGAAA | 9051 |
| rs564708944 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037283 | GCGTCCCCCAGCCCC[A/G]AGAGGGAGCCTGTCG | 9051 |
| rs564755163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031405 | TGGCCCCAGGGGTCT[C/T]AGGCCTCAGCAGCTC | 9051 |
| rs564763278 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028210 | CCTGAGCTTGATCCT[C/G]CGAGACGCTGGACAG | 9051 |
| rs564818445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026724 | CTAAATGTGGGGTTC[A/T]GAGCAGACAGGGGGT | 9051 |
| rs564867887 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030916 | CTCCCGTCCGAGGTC[C/T]CTCTCACTACCCTTC | 9051 |
| rs564896429 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999989 | GGTCACATGCACTGC[A/T]GTGACTGTCACCCAC | 9051 |
| rs564903733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023394 | CTGGAAGCAACGGGC[A/G]GAGGGGCAGAGAGCA | 9051 |
| rs564916565 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999822 | GGTCCCCCATCCCCC[A/G]CAACCTGTATGTCTA | 9051 |
| rs564927254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029631 | TGGGCGGTACTCCCC[A/C]CACACACCTCCTCAC | 9051 |
| rs564967672 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023789 | CTGGAGGGTGGTGTG[A/C]GTAAGGGCTGGGTTG | 9051 |
| rs564988714 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033628 | TGCCTGTGCCCCCAC[C/T]GCCATGCCACCACTC | 9051 |
| rs565024179 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022356 | AACACACTGGAAATC[A/T]GGACTGTATTTGAGC | 9051 |
| rs565052503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004917 | AGAAGCAGAGAGCCA[A/G]ATCTTGTAGGACTGT | 9051 |
| rs565073285 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995004 | AGTGAGCCCGCACCT[C/T]GGGAGGGGGCAAGCA | 9051 |
| rs565180192 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008992 | CCCAGTGGCCCGCTT[C/T]GATCCTACTACACTC | 9051 |
| rs565188429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030343 | CCAGCGTGGGTGGCC[C/G]TGACGGGCATTCAGA | 9051 |
| rs565251211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024785 | ACCTCTCAACTCCTG[C/T]GCCCTGCCCTGCTAG | 9051 |
| rs565286492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76999558 | TGCTGGGATTACAGG[C/T]GTGAGCCGCCGCGCC | 9051 |
| rs565287616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034823 | CCCCCAGCATCTGCC[A/G]CATCTGCCTCTTCTG | 9051 |
| rs565337910 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012144 | CCATCCATCCATCCA[C/T]CCATCCATCCATCCA | 9051 |
| rs565387317 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003739 | CTAGGTGGCCTTGGA[G/T]AATCATTTTCCCTTT | 9051 |
| rs565395583 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030654 | CCTACTCCAGCTGCT[C/T]AAAGGGGCCCAAGTG | 9051 |
| rs565617481 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037703 | AGGTTGGGGGTACAC[A/C]CAGGAATATTCGGAG | 9051 |
| rs565626365 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036427 | AATGAGTCTTGCTAT[C/T]GTGCCAGGATTGATT | 9051 |
| rs565629482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005805 | GCTCATCCATGTCAT[A/G]GCATATGTCAGAATT | 9051 |
| rs565643919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999237 | GGACAGTGAATGTCT[C/T]CATGGTCCATCTCCC | 9051 |
| rs565671788 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014621 | GTCTGTGGTCTCGCC[C/T]CTGCAGCCACCAAGA | 9051 |
| rs565708262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011890 | TTCCTTGCATTGTCC[C/T]GGAGTTGGCCTCCCT | 9051 |
| rs565722138 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012842 | GGTCCCCTCCATGGG[A/G]CACCTCAGGAAGCAG | 9051 |
| rs565785437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006342 | TGAGTTGAAGGAGTT[A/C]TTTATATTTTCTAGA | 9051 |
| rs565918390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023440 | AGGTGGAGGTGGTGC[A/G]GCAGGGGCTGCAGCG | 9051 |
| rs565933998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017308 | AGCAGCTCAGACACA[C/T]ACCTGGAATCCACTG | 9051 |
| rs565974851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018572 | CACTCCTCTCCTCTG[C/T]TGGCAGTTTCTGGGC | 9051 |
| rs566055264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019617 | GCTCTGGTCCCGGCT[C/T]GGCCAATCTGAGCTG | 9051 |
| rs566088503 | in-del | -/TCCA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012156 | CCATCCATCCATCCA[-/TCCA]CCCACCCACCCACCC | 9051 |
| rs566101272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025013 | TGCAGCTAGGAGCAC[A/G]GATGGTGGGGGCCTT | 9051 |
| rs566162502 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019108 | GTTAGAGGGCAGGCC[A/G]TCAGGGAAGTGGCTC | 9051 |
| rs566232143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76999575 | TGAGCCGCCGCGCCC[A/G]GCACTACATTTCACT | 9051 |
| rs566241921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033833 | AGGGCACACACACAC[C/T]CTCTTTGAGAATCTT | 9051 |
| rs566243222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015736 | GGCAGGGGTGGGGGT[A/G]AAGGAGGAGGGCGCG | 9051 |
| rs566277115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034394 | CGCATGTCCACCCTG[C/T]GCATGTGTGTGCACT | 9051 |
| rs566286119 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994546 | CCCATTCACTGAGCC[A/G]GAAGCCTCCATCTTC | 9051 |
| rs566342772 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993948 | AGGTGAGGGCCTTCT[A/G]GGGGCAGTCCCATTG | 9051 |
| rs566364717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034931 | AAGTAGCCCAGCGCT[A/G]TCCCGGAACTCCTGT | 9051 |
| rs566384698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027316 | GACCTCGGCACAGGG[G/T]CCCAGTGGCCACTGT | 9051 |
| rs566401416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030367 | ATTCAGATGAGGCCC[C/T]GCCATCTGCTAGGGC | 9051 |
| rs566406881 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996532 | GCTCAGCCGGCTGAG[C/T]CCCAGCCAACAGCCC | 9051 |
| rs566438873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026897 | GCACTGGCTGCAAAG[C/G]CTGTTTTGGACAGAG | 9051 |
| rs566452622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032118 | AGGGCCTTGCACACA[C/G]AAGGTGTTCAGGAAA | 9051 |
| rs566589576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033237 | GGCTTCCTTGTCCCT[A/G]GGGCCTCATGTGAGC | 9051 |
| rs566664567 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025035 | GGGGGCCTTCGGTAC[C/T]TCCTCCTTCTGCCAC | 9051 |
| rs566721845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036393 | CTTCGTGGCCATGGG[C/T]GTGGAAAACTGTGGC | 9051 |
| rs566736298 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031643 | GCTCTAGGCCTGGTG[C/T]TTGCAGGAGCCGAGG | 9051 |
| rs566754205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009946 | ACCACTGGTGCCCCT[G/T]GCTGGTCACTCACAG | 9051 |
| rs566808654 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002156 | CCCAAACGCATTGTC[A/T]GTGTCTTCCTGACTC | 9051 |
| rs566817359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010305 | CAGTACTAACTTGAC[A/G]GGGTTCCCTGAGGAC | 9051 |
| rs566906535 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037297 | CGAGAGGGAGCCTGT[C/T]GTCTCCCAGGGAATA | 9051 |
| rs566911498 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008583 | CCCGGCTAATTTTTG[G/T]ATTTTTAGTAGAGAT | 9051 |
| rs566918670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028261 | GAGGGCGCGGCGTGG[C/T]GAGGGGCGTGGCGAG | 9051 |
| rs566934838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998632 | TGGACTACGAAAGGA[C/T]GTTTCACAGGCAGCT | 9051 |
| rs566989031 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004016 | TATACTCCACCATTA[C/G]AGAATCATTCCTTTG | 9051 |
| rs567028705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010374 | ACACTCAATCCCTTC[C/T]CCTGAACCTGGAACC | 9051 |
| rs567047605 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029465 | ACAGTCACTTCAGGT[C/T]TGCTGGGGTGGGCCC | 9051 |
| rs567173307 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010803 | ATGTGCCCGCCACTA[C/T]GCCCAGCTAATTTTG | 9051 |
| rs567279467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999024 | ACCAGCTGTCTGAGC[A/G]GAGAGGGCACTGGCC | 9051 |
| rs567368032 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028921 | CTGAGGCCCACAGGG[G/T]GATGAGAGCAGACGC | 9051 |
| rs567380193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029474 | TCAGGTCTGCTGGGG[C/T]GGGCCCTGGCTCCTG | 9051 |
| rs567441250 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023460 | GGGCTGCAGCGGTGG[G/T]GGCAGCTAGCGTAGG | 9051 |
| rs567489344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003827 | GCTTTGAGGTTGGGG[C/T]GGCTCAGGGCAGTGC | 9051 |
| rs567489599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011015 | ATTGGGCTGGCCCCA[G/T]GAGAGTGAAGGAGGG | 9051 |
| rs567491747 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996160 | GTTCCCCTCACCCAG[C/G/T]CCCTTGTCCCTTGCA | 9051 |
| rs567513132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032188 | AAGACCCCGAGCCGC[A/G]CACAATGGCCTGTGA | 9051 |
| rs567515563 | in-del | -/CATC/CATCCATC | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012529 | TTCCATCCATCCATT[-/CATC/CATCCATC]CATCCATCCATCCAT | 9051 |
| rs567525325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027421 | ACAGGAATGCCTGTG[A/G]TCATGCGTGTGGGCA | 9051 |
| rs567527279 | snp | A/G | 0.000438657 | 0.0148032 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032454 | CCCCTGGGAAGGCCC[A/G]GCCCTGAGCCTCAAG | 9051 |
| rs567557614 | in-del | -/GT | 0.0069072 | 0.05836 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031309 | TTGGTGTGGGGTAAG[-/GT]GTAGGGCAGCCTCTA | 9051 |
| rs567571287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021869 | TGTCACCTCCCTCAG[A/G]AAGCTGTCACCTCCA | 9051 |
| rs567589529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028078 | TGCGGGGCGCTTGGG[C/T]CCGTGCTGGGCGCTA | 9051 |
| rs567671329 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993181 | TGAAAAGCAGAATGA[C/T]GTACCCGGTGCTGGG | 9051 |
| rs567764739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030892 | GGGCCTGGGGAACAG[A/G]GCTCAGGACTCCCGT | 9051 |
| rs567776617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031121 | CTGTGAATGGGGCCC[A/C]GCCTGGCCGGGCCCT | 9051 |
| rs567837783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026386 | GCTTCTTGCCTGGGG[A/T]GGAAGGATCGTTGTG | 9051 |
| rs567893030 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035677 | GAAGTGTGTGTCCCC[C/T]AACAGCAAGTGTGGA | 9051 |
| rs567914058 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033698 | GGTAGTGGACTGTGG[A/G]GAGAGGCTGATGCAG | 9051 |
| rs567930727 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001642 | CTGCATCTGTCAGAA[A/G]CAGTGAGGACGGAGG | 9051 |
| rs568005094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007840 | ACCTCGTGATCTGCC[C/T]GTCTAGGCCTCCCAA | 9051 |
| rs568015790 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995417 | CAGAAGCTCCTCTCT[A/G]GCTCGTGGCTGCCTT | 9051 |
| rs568102417 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021420 | ATTAGGGCCAGGCGC[C/T]GTGCCTCACGCCTAT | 9051 |
| rs568241900 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019228 | ACACAGCCACCCTAA[C/G]AGTGGAGTGGAGGGG | 9051 |
| rs568347687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001058 | GCAACACCACTGTTC[A/G]TGGCTGCACAGTTCT | 9051 |
| rs568352947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026770 | CAGGCTTGAGGTGCC[A/G]GAGCAGGCACCCTCT | 9051 |
| rs568366864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76999571 | GGCGTGAGCCGCCGC[A/G]CCCAGCACTACATTT | 9051 |
| rs568435633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009119 | GAGTGGAGACATGCA[A/G]GTTAATGGCCAAGCA | 9051 |
| rs568475057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996504 | AACCCCGAAGAGGAC[A/G]CTCTGGCCCTCGGCT | 9051 |
| rs568503340 | snp | A/G | | | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018500 | GAGCTGGTGCAGATC[A/G]CACGGAAGGCAGGTG | 9051 |
| rs568550396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002500 | AATGAGTTGGTGTTT[C/T]TAGGCCAAATTTGTG | 9051 |
| rs568555393 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026532 | TCTGTGCCTCAGTTT[C/T]CCTCTCACAGGATGG | 9051 |
| rs568569800 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026833 | GAACCTGCCAGGAAG[A/G]AGGGACCCCGGCCCT | 9051 |
| rs568616238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003094 | CTGCCCTAAGTGGTG[G/T]CAGAGATACTTTCTT | 9051 |
| rs568632534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021217 | CGGGAGCCACCCTCA[C/G]GCCTGGAGGCTCGGG | 9051 |
| rs568657995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021089 | GAACAGGGTGCAGAA[C/T]GAGGACAAAAGCCAG | 9051 |
| rs568670467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015090 | CCTCTGACCCAGCCT[A/G]GGCCCCAGGCTAGCC | 9051 |
| rs568686190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001179 | CTGGACAGTGACACC[A/G]TGGGTAGATCTTTGA | 9051 |
| rs568804023 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031606 | CAGAGGTTGGCAGAA[C/G]CTGGAGGACCGTGGC | 9051 |
| rs568816115 | snp | C/T | 1.69634e-05 | 0.00291229 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031142 | GCCGGGCCCTGCAGC[C/T]GCCTCCTCACTGCTC | 9051 |
| rs569030059 | snp | C/T | 1.89572e-05 | 0.00307867 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025575 | AGTCTCGAGGAGTTT[C/T]GTGAGAGGCAGAAGG | 9051 |
| rs569168126 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027079 | ATATGCCTGTGAGCA[A/T]GTGTCCTTGTCCAGC | 9051 |
| rs569300580 | snp | A/G | 4.15119e-05 | 0.00455568 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032248 | GAGTTCAGGCCCACA[A/G]AGGGGCAGAGTGGGC | 9051 |
| rs569360804 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997358 | TCTGGGCCGATGCCC[C/T]GAAAGGTCACTGTAG | 9051 |
| rs569467801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015327 | TCTGCCCTTTACCCA[C/T]TGAGTGGCTTTGGGC | 9051 |
| rs569547433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024024 | GCAGGGTGGCCACGG[A/G]CGCAGCTCCTTCACT | 9051 |
| rs569548271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012400 | CCATCCATCCACCCA[C/T]CCACCCATCTACCCA | 9051 |
| rs569549438 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037449 | CTCCCCAACTCAGCC[G/T]AGGCTTCAGCTATAG | 9051 |
| rs569632059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034428 | GGGGCCTTGGCCCTC[A/G]GCGCCTCATGTGGGA | 9051 |
| rs569644776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006405 | ATATTTTCTCCCACT[A/C]TGGAGTGTCTTTTCA | 9051 |
| rs569667992 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001379 | TCACACAGGAAGGAG[A/G]GACCCCAGAATGGCC | 9051 |
| rs569685600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033186 | CCAATTATTCACTAG[A/G]GGAGGTGCTCCGAGC | 9051 |
| rs569750076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007089 | CACTTGCTTTAGAGG[G/T]CCCCTGGGTTGTGGG | 9051 |
| rs569767739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010938 | GTTGTGAGCCACCAC[A/G]TCCAGCCCTCTCTCT | 9051 |
| rs569782964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017962 | TACCTGTCACCTCTG[A/C]AGATGTGAGGGGACC | 9051 |
| rs569851704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012048 | TTGGAACTCTCCCTT[C/G]CCTCCCTATCACCTC | 9051 |
| rs570058927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014388 | GGCTGAGAAGGGCCA[A/G]GGTCACGGGAGGTGT | 9051 |
| rs570146102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007904 | CGACTGGCAATAGAA[C/T]ACTTTGAGGACTGCA | 9051 |
| rs570161322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035120 | GAGCAGGGGCCTGGA[A/G]GGTGAGGACTGGGCA | 9051 |
| rs570198100 | snp | C/T | 0.000238336 | 0.0109138 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035459 | TCCCTCCTGGTGGGT[C/T]CCTGAGTGTGGGGCG | 9051 |
| rs570199468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035063 | TTGTGTGGCAGTGCA[A/C]CCCCCACCCCTACCC | 9051 |
| rs570215401 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006103 | AAAAGGGATCCAATT[A/G]CTCCATATCTTTGCC | 9051 |
| rs570320785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025144 | CCATCTGGCTAAAGG[G/T]TCCCTTGGTTCTAGA | 9051 |
| rs570341727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019031 | TTTCCTCATCAGTGA[C/T]GGGAAAGTAACGCAG | 9051 |
| rs570383972 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019123 | GTCAGGGAAGTGGCT[C/G]TGATGAAGCGGGAGT | 9051 |
| rs570416817 | snp | A/G/T | 3.46802e-05 | 0.00416403 | synonymous-codon, missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030557 | CCGGGCTGAGTGGGA[A/G/T]CAGGAGCACCGGACC | 9051 |
| rs570524239 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997011 | ATCACTGAGACCTCT[A/G]TCCAGTCCTAGAGCC | 9051 |
| rs570538447 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76994777 | GTTTGGGTCCCAGAG[C/T]AGCCAGGGTTTGATG | 9051 |
| rs570584882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012689 | CTTAGCATCCCTGTG[C/T]CTCTGTTTCCGTATC | 9051 |
| rs570599592 | snp | A/G | 0.000883002 | 0.0209934 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995373 | TGATTCTAGCCCCAA[A/G]CAAAACAGGTTGAGC | 9051 |
| rs570644424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006481 | TCTACTCTTTGTTTT[A/G]TTGCCTATGATTTTA | 9051 |
| rs570726391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007163 | CCATCTATGACATCT[C/T]GGCTTCCTTGAGGCC | 9051 |
| rs570820056 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001729 | AGAGAGCCTGGCAGT[G/T]CACCTGGTCGGCAAC | 9051 |
| rs570888731 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000173 | TAACAGGTGACAGCA[C/T]CGCTGCCGAGTGGGG | 9051 |
| rs570911860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008556 | CTGGGATTACAGGTG[C/T]CCGCCACCACACCCG | 9051 |
| rs571003466 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030848 | ACTTGGACTAAACCC[A/C]CAGCCTCTCTGGGTG | 9051 |
| rs571065383 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025721 | CGGCAGGGGTGGTGG[G/T]GGGACAGCACTCCAG | 9051 |
| rs571162751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027347 | GCCTGCATGTGGCCT[A/G]TGGTTGTGTGTGGGT | 9051 |
| rs571178503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020585 | GTGCCATGCCCTGGA[C/T]GGGTCAGGAGGATTC | 9051 |
| rs571245169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011142 | GGTCAAAAGCCAGAC[A/G]CCCCACAACATTAGA | 9051 |
| rs571267527 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993800 | TGGGAGGTGAGGTGC[A/T]GCCTGGCTCACTCTA | 9051 |
| rs571291012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017230 | CCTGGGAGACCTCTG[C/T]TCCTTCATAGTCCTT | 9051 |
| rs571295008 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007670 | CACAATCTCAGCTCA[C/G]TGCAAGCTCCGCCTC | 9051 |
| rs571322405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011721 | GTCAGGGGACCCCTA[A/G]ACACCAAGTCCCTAG | 9051 |
| rs571334172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032487 | CCAGGACCGGGCTGG[A/G]GTAGCTCACAGCTCC | 9051 |
| rs571360599 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034730 | ACTCAGCCCCACCCC[A/C]CTAAGAAGCCCTCTT | 9051 |
| rs571471617 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998700 | GAAAAGCAGCTGTAG[A/T]GGCACAGAAGTAGTG | 9051 |
| rs571520748 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022259 | GGCTCATCGTGGGCA[A/C]AGCCTCAGCACAGGG | 9051 |
| rs571529866 | snp | C/T | 0.000460158 | 0.0151614 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029525 | TTCCCCTCTGTTTCC[C/T]CAGAGTCAGAACAAA | 9051 |
| rs571594818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999138 | CAGGTGGCCAAATTA[C/T]TGCAAGAAATGTCTG | 9051 |
| rs571656765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029900 | TGAACCCAGGCCATC[A/G]GGCTTCAGAGCCCAG | 9051 |
| rs571657181 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993270 | TAAGGGTGGAAGGGA[A/G]GGGAGGAGGAAGGCC | 9051 |
| rs571668906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024188 | TCAGGAGGTCGGGGA[A/G]GAGCCTGAGAATCTG | 9051 |
| rs571916098 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037675 | GGCCAGGGCAAGTGC[A/G]TGGGCAAAGGTGAGG | 9051 |
| rs571976850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998190 | TTGCAGTGAGCTGAG[A/G]TTGTGCCACTGTACT | 9051 |
| rs572048062 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037442 | TGTGGAGCTCCCCAA[C/T]TCAGCCGAGGCTTCA | 9051 |
| rs572080370 | snp | A/G | 0.000144571 | 0.00850087 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033001 | GCTGGGCCAGGAAGT[A/G]GGTCGAGCCCCTCCT | 9051 |
| rs572140564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012199 | CCCATCCACCTGTCC[A/G]TCCATCCATCCGTCC | 9051 |
| rs572143373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033372 | TGCAGTCAAGTGCCA[A/G]GGTCCTAGTGCTGGG | 9051 |
| rs572175357 | snp | C/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036212 | GCAGCAGGCCTGTGT[C/G]TGCCCGGGCCTGTAC | 9051 |
| rs572203976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006055 | AACTTTTTGAGTAAC[C/T]GCCAAACAGTTTTAC | 9051 |
| rs572242536 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015692 | TCCCAGCTCAGAGCA[C/T]GGAGTCAGACCCATG | 9051 |
| rs572266965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004142 | TGAGCCTCTTGGAAG[A/G]AATGTGGGCCTGGGG | 9051 |
| rs572454830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999427 | GGGATTACAGACGTG[C/T]GCCGCCACGTCTGTC | 9051 |
| rs572620087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009413 | ACAGCAAATCACAGC[C/T]GCAAAGCAGGCACCT | 9051 |
| rs572658415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023701 | ACCCAAAAGGTGAGG[G/T]CGGGGAAGTGGATGT | 9051 |
| rs572721166 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018171 | CTTCACAGCCCACAC[G/T]GGCTACGAGGTGCTG | 9051 |
| rs572726029 | snp | C/T | 8.32813e-05 | 0.00645242 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029592 | ATGTGGGCCTGGCTG[C/T]CCCGTCCGACCAGGG | 9051 |
| rs572726889 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020880 | CTGTGGGGGGGGGGG[G/T]TGTGTGTGTTGGCCC | 9051 |
| rs572766839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020292 | TCTGCCCTGACTTAT[A/C]CTTTGTGTGGCCCTG | 9051 |
| rs572911084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002211 | GGTCTAGGCCCAGAC[A/G]AGGGTCACCTGTGCA | 9051 |
| rs572995547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026030 | CCCCACAGGACTGCC[C/G]AAGGCTGAGGGGTCA | 9051 |
| rs573018307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026557 | GGATGGGACACATAT[A/G]TCTACCTCCCAAGTG | 9051 |
| rs573079957 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998370 | TGGCTTTAGCTCACA[A/G]TAAGGGAGGAAGCAA | 9051 |
| rs573105212 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025824 | CTTAGTCCCAGAGCC[C/G]CATGGAAGGTCCTTC | 9051 |
| rs573106329 | in-del | -/GA | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036084 | AGGGCACGTGTGCCC[-/GA]GTGTGTCCACACTAG | 9051 |
| rs573139638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036617 | CTCCACTGATGAGGC[C/T]AGGGCTCGGGGAGGC | 9051 |
| rs573176123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036842 | AAGAAACCCAGGTTG[C/G]GGGAGAACTATGATG | 9051 |
| rs573177137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027046 | CAGGATGGTGCACAC[A/G]TGCCTACGCTCCCCT | 9051 |
| rs573217224 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022005 | GCCAGCTTCCTGTAG[A/C]CCCTCTGTGGTTACC | 9051 |
| rs573309941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022421 | TCAAAAAGGGCAATG[A/G]GATGAGTTACACATG | 9051 |
| rs573338044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009512 | CAGAGAGTGGGAGCC[A/G]CTAGTCTAGAGAAGT | 9051 |
| rs573364556 | snp | A/G | 0.000141014 | 0.00839566 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027705 | CACTGTGAAGCAGCA[A/G]GCTCTGGGGGAGGGA | 9051 |
| rs573366367 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003152 | GGCTGTTTCCTCTCA[C/T]GCAAAAGAGGACAGA | 9051 |
| rs573408926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003423 | TCTTGGGAGGCCGAG[A/G]CGGGTGGATCATCTG | 9051 |
| rs573540691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022065 | AAGTTTGAATCCTCA[C/T]GTCCCTGCCTCACCC | 9051 |
| rs573591710 | in-del | -/CACCAACACC | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014748 | CTGGGCCGTGGCTCA[-/CACCAACACC]CACCAGAGAATGAAG | 9051 |
| rs573679707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028422 | CCAGATCCCTGTCCC[C/T]GGTGAGGATGCCCCC | 9051 |
| rs573743335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022525 | GTAGAGGTGCTCAGG[A/G]AGATCTTGACAGTTT | 9051 |
| rs573784011 | snp | A/G | 0.000432598 | 0.0147007 | splice-donor-variant | PSTPIP1 | GRCh38.p7 | 15:77025319 | ACTCCTTGAAGCAGC[A/G]TAAGTCCCCTACCCT | 9051 |
| rs573811462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021418 | GCATTAGGGCCAGGC[A/G]CCGTGCCTCACGCCT | 9051 |
| rs573823522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020992 | GGCCTCCCTGAGGCC[C/T]ACAGCTGCCCCCCAG | 9051 |
| rs573863833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031701 | TCCAGGGTGTCCTGG[C/T]TCCCCTTACTGAGCC | 9051 |
| rs573863923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026616 | CTCAGTCTCCACAGA[C/T]AGGGCTCCAGCTCTG | 9051 |
| rs573872239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015427 | ATAACGCTATGATAC[A/C]CTTGGTGCAGTGTGT | 9051 |
| rs573951876 | in-del | -/AGG | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035302 | GGGCGTAGCTGGGGA[-/AGG]AGGAGCCACCAGGAC | 9051 |
| rs573965425 | snp | C/T | 0.00312051 | 0.0393766 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027768 | AGAGGTGCTGCGCCT[C/T]ATCCCAGGGACACTC | 9051 |
| rs574074119 | snp | G/T | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010674 | TTCTTTTGAGACAGG[G/T]TCTTACTCTGTCACC | 9051 |
| rs574093502 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009610 | TGCATGAATCCCCTC[A/G]GCTGCCCTTCCAGGA | 9051 |
| rs574099259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017475 | AGGGTGTGCTTGCGC[A/G]TGCTCTGACCTGGAC | 9051 |
| rs574421832 | snp | A/C/T | 0.000633328 | 0.017784 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025366 | TTGGGACTGCGAGGC[A/C/T]GGTGGAGGGTTTGGG | 9051 |
| rs574546705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999807 | TGCCATCCTCTCCCA[A/G]GTCCCCCATCCCCCG | 9051 |
| rs574609703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013520 | CCCTTTCTCTCCCTG[A/G]CACCTGGGCAGGTTT | 9051 |
| rs574623147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035158 | ACGAGGCCTCAGTGC[A/G]GAGGTCCTAGAACCC | 9051 |
| rs574627310 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000462 | GCATTTAAAGAGAGA[G/T]ATATATATATATATA | 9051 |
| rs574627519 | snp | C/G/T | 1.94805e-05 | 0.00312087 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995394 | CAGGTTGAGCTTTTT[C/G/T]CTCCCCTCAGAAGCT | 9051 |
| rs574687880 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994846 | ATGACTTGCTAGTGC[C/G]GGGTGGGGAGTCTGG | 9051 |
| rs574690094 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036260 | CACATGTACCTATGC[C/T]GTCCACACAGGCTGG | 9051 |
| rs574731012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035733 | GCATGGAGAAACCCC[A/G]TTCTAGTAGGACTTC | 9051 |
| rs574747436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995668 | GAGCTAGGCTGAAAT[A/C]TCCATGCAGGTGATG | 9051 |
| rs574797740 | in-del | -/GT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020888 | GGGGGGGGTGTGTGT[-/GT]TGGCCCTCAGGAAAG | 9051 |
| rs574948601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020853 | GTGGACCTGTTTCCT[C/T]ATCTTAGACTCCTGT | 9051 |
| rs574957138 | snp | A/C/T | 3.34126e-05 | 0.00408722 | synonymous-codon, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031204 | CTGCAAGAGTTTGAC[A/C/T]GGCTGACCATTCTCC | 9051 |
| rs574970063 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013996 | GGGAAGGTGTTTCTG[G/T]TCGGGGAGGTGGCAG | 9051 |
| rs575117315 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007626 | TTGAGATGGACTCTC[C/G]CTCTGCTGCCCAAGC | 9051 |
| rs575161638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025431 | GCTGGCCCACACGGG[C/T]GAGTTGTGGGTGGCT | 9051 |
| rs575195512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036507 | ATGAGAGTCCTTTCT[A/G]CTCCCTGCTTGAGGG | 9051 |
| rs575217513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008568 | GTGCCCGCCACCACA[A/C]CCGGCTAATTTTTGT | 9051 |
| rs575253270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014172 | GCACCCGGCAGGTCC[C/G]TGGGCAGATTGGGTA | 9051 |
| rs575259407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014542 | GGGGTTAGCCTCCTG[A/C]CCCCACTTTCCCAAT | 9051 |
| rs575312731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008348 | CAGAAATTTCATCCC[C/T]GTCCTCAGATAACTC | 9051 |
| rs575354672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035207 | CTTCCAATGAAGCTA[C/T]AGCTTCGGGGGTTCT | 9051 |
| rs575371049 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994933 | GGTTCCTGGGCCCCT[C/G]CTGGCCACACTGTCA | 9051 |
| rs575399821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030605 | CCCACGTGGAGCCTC[A/G]TTTTCCCCAGCTGGG | 9051 |
| rs575417439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030907 | GGCTCAGGACTCCCG[A/T]CCGAGGTCCCTCTCA | 9051 |
| rs575505468 | in-del | -/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037706 | TTGGGGGTACACCCA[-/G]GAATATTCGGAGGAC | 9051 |
| rs575553522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031769 | CCCAGCCAGGGTCCC[C/T]GAGCTCTGTGGATGG | 9051 |
| rs575555911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036239 | GTACACAGCACACAC[A/G]TGGAGCACATGTACC | 9051 |
| rs575585236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031354 | CAGGTCCATCTGAGC[C/T]GGTCAACAAGCACCT | 9051 |
| rs575616847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027006 | TGTGTATGTGCGTGT[C/G]CCACAGAGCAAGGAC | 9051 |
| rs575645219 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002668 | TTTGTGGTCATGCTT[C/G]CTTTGCTTTTGCGAT | 9051 |
| rs575683835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996703 | AGTAGGCAAAGGACC[C/G]CACGTGGGGAGGGCA | 9051 |
| rs575770055 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016344 | TTTCTTCCCAGCCGC[C/G]AGGAGCTCTGACCTG | 9051 |
| rs575776396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008657 | TCAGGTAATCCACCC[A/G]CCTCGGCTTTCCAAA | 9051 |
| rs575807101 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017360 | GGTTGGCCAGGAACA[A/G]CAGCCAGGGCAAGCA | 9051 |
| rs575997673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002191 | ATGGGACCTAAGGCA[C/T]GGCAGGTCTAGGCCC | 9051 |
| rs576033153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034047 | AGGATTAGAGAGAGA[A/G]AGAGAGATGTCCTGC | 9051 |
| rs576072252 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993410 | GGACAGGTACAGTTG[G/T]GAAAGGAAGGCCTCA | 9051 |
| rs576126794 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007437 | GCATGGCAAAACCCA[A/G]TCTCTACAAAAAATA | 9051 |
| rs576317993 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008934 | CAACATAGAAGCCTT[C/T]ACTTGGCAGGCGCCA | 9051 |
| rs576366654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013431 | GTGGGGCACAGGCCG[G/T]GACTGTAAAGGGGAG | 9051 |
| rs576413796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998865 | GTAGGAGTGAGGCAG[A/G]GCGGACCAGCCACAG | 9051 |
| rs576415591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005909 | ATGACCACTGGGCTG[C/T]TTCTTTGAGCTACTG | 9051 |
| rs576504941 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033859 | ATCTTGTGCAAGCAG[G/T]GACCCCAGGAGGCAG | 9051 |
| rs576525828 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011695 | TATACATGGATCGCA[A/G]CAGTACTTGAGTCAG | 9051 |
| rs576601123 | snp | A/G | 8.32882e-05 | 0.00645269 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018281 | CCATGGGGAGCGCAG[A/G]CAGGAAGCAGGTGGC | 9051 |
| rs576634766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018682 | TGGTTATTGGGCATT[C/G]AGGGTGAGGCCAGGT | 9051 |
| rs576690483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023757 | CTGGGTATGCTGTGG[C/T]CATGAAGGAGGCGGG | 9051 |
| rs576751406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034103 | GAGGGGGCTGGTCAG[A/G]CCTCTGGATGGGGCA | 9051 |
| rs576755793 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024381 | GGTGTCTACTGAGAG[A/G]AGAAGCCCCCTGAGA | 9051 |
| rs576834348 | snp | G/T | 0 | 0 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024498 | CTCCACAGAGAGGCT[G/T]CAGGGAGAGCCAGAT | 9051 |
| rs576855562 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022772 | GAGCTGAACTAGGGT[A/G]GCCTGATGGTTCCAG | 9051 |
| rs576919287 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995005 | GTGAGCCCGCACCTC[A/G]GGAGGGGGCAAGCAG | 9051 |
| rs576994176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006025 | ATTGCTGGATCATAT[G/T]GTAATCCTATGTTTA | 9051 |
| rs576996199 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999958 | TAAAAGGAAAAGTAA[A/G]GACCTGGGGAGGCTG | 9051 |
| rs577191525 | snp | A/C/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037635 | CGGAGGGTTGAGCAG[A/C/G]TCCATGGCTGGGCAG | 9051 |
| rs577198611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77008042 | AGGTGGTAGGAAGAC[A/C]CAGAACAGCTGAGGA | 9051 |
| rs577199005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000737 | TGCAGAGATGAGGTC[C/T]CCCTGTGTTGCCCAG | 9051 |
| rs577199534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999327 | TCTGTCACCCAGGCT[A/G]GAGGGCAGTGGCACA | 9051 |
| rs577209855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999731 | CCATAGTTCAGTGCC[A/G]GGGCTGGAGGAATAA | 9051 |
| rs577349507 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035215 | GAAGCTACAGCTTCG[C/G]GGGTTCTAGGATCCT | 9051 |
| rs577482804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007543 | GAGCCCAGGAGGTCG[A/T]GGTTGCAGTGAGCTG | 9051 |
| rs577491691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018749 | AAAGGGTCTGGGCAG[A/G]GGAGACAGGAGGCCA | 9051 |
| rs577551104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019197 | GGCCAGGTGAGGAGA[A/T]GAAGGTGAGTTCAGG | 9051 |
| rs577552921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013115 | GATGTCACTGCTGGT[A/G]TGAGGGAGGAGAGCA | 9051 |
| rs577563539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013428 | GTGGTGGGGCACAGG[C/T]CGTGACTGTAAAGGG | 9051 |
| rs577591958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003452 | TGAGGTCAGGGGTTC[A/G]AGACCAGCCTGGCCA | 9051 |
| rs577592685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010426 | CCTGGGAAGGTCCTG[C/T]CCTTTGCTGTGTGTG | 9051 |
| rs577653369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017551 | GGTTTCCTGAGCCCA[C/T]AGAGAGCCCAGCGCA | 9051 |
| rs577668796 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029299 | TGTGGTCTCACTCTT[C/G]ACAGGCATCCTCCTG | 9051 |
| rs577693562 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000889 | TATTTTAAATTGTAG[C/T]GAAATACACATAAAA | 9051 |
| rs577696314 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025652 | CCCCCATTGCCAGCC[C/T]CTCAGTTGCTGTGGG | 9051 |
| rs577746056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027513 | AGAGTGTACACACAC[C/G]TGTGAGCGACTGTGA | 9051 |
| rs577835318 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037186 | CTTTGAGGAAGGGCC[A/G]GGAGCCCCTTCGGAC | 9051 |
| rs578047059 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005021 | ACATCAGTATTTTTC[A/G]AAGTTCCCCAGTGCC | 9051 |
| rs578058660 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012131 | TCCATCCATCCATCC[A/G]TCCATCCATCCATCC | 9051 |
| rs578074157 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028376 | AGGACTACCAGCAGC[C/T]CCCACGCCTTCTCTA | 9051 |
| rs578103911 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011071 | GGGGTGCTTTCCTGC[C/T]TCATCATTGAGAAGG | 9051 |
| rs578125746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033323 | CATCTGGAGAATTCT[A/C]CAGGCTTTTCCAGGG | 9051 |
| rs578170522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029078 | CAGGTGGTCTAGAGC[C/T]CATGCTCCTGATGCT | 9051 |
| rs745313790 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008954 | GGCAGGCGCCATCTT[C/T]GTCTCTCACTCTGAC | 9051 |
| rs745343304 | in-del | -/AG | 7.63038e-05 | 0.00617625 | splice-acceptor-variant | PSTPIP1 | GRCh38.p7 | 15:77029527 | CCCCTCTGTTTCCTC[-/AG]AGTCAGAACAAAGCC | 9051 |
| rs745356789 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999125 | GCTCCACTCCCAGCA[-/G]GTGGCCAAATTATTG | 9051 |
| rs745393110 | snp | C/G | 5.17719e-05 | 0.00508756 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025470 | TCAGATCTGACACTG[C/G]GGACCAGTATCCATG | 9051 |
| rs745431027 | snp | A/C/G | 9.62429e-05 | 0.00693642 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037198 | GCCAGGAGCCCCTTC[A/C/G]GACCTGCCCTGCCAG | 9051 |
| rs745476563 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018897 | CAGCATGGGCTTCAA[C/G]GATGGAGATGTAGCC | 9051 |
| rs745486341 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029972 | TGATGCCCGAATCCT[A/T]CCAACACTCTTGTCC | 9051 |
| rs745534526 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003723 | CCCTCACCCACACTT[G/T]CTAGGTGGCCTTGGA | 9051 |
| rs745709150 | snp | C/T | 0.00249955 | 0.0352637 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007826 | GTCTCGATCTCCTGA[C/T]CTCGTGATCTGCCCG | 9051 |
| rs745721337 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002427 | AGTCAATACAGAGTA[A/C]CTTTGTCATTAAAAA | 9051 |
| rs745724652 | snp | A/C | 1.67061e-05 | 0.00289011 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031308 | CCTTGGTGTGGGGTA[A/C]GGTAGGGCAGCCTCT | 9051 |
| rs745809837 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023209 | TGAGGAGGAGAGCCA[A/G]GCATTGCCCCTGTCC | 9051 |
| rs745993601 | snp | A/G | 0.000171292 | 0.00925291 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032480 | TCAAGTGCCAGGACC[A/G]GGCTGGGGTAGCTCA | 9051 |
| rs746024823 | snp | A/G | 3.6245e-05 | 0.0042569 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035773 | GTGTCCCCAGAAGGG[A/G]AGGGGTCTATGTCTC | 9051 |
| rs746073019 | snp | C/G | | | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994945 | CCTCCTGGCCACACT[C/G]TCAGTGGGCCTCAAG | 9051 |
| rs746076648 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032065 | TGGGAAAAGTGGGGT[A/C]TACCTTAGAGGACAG | 9051 |
| rs746091084 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006337 | ATTGTTGAGTTGAAG[G/T]AGTTCTTTATATTTT | 9051 |
| rs746168558 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016778 | TGGAGAATACCTTCT[C/T]CTTCCAGCACCTGAC | 9051 |
| rs746251229 | snp | A/T | 3.57865e-05 | 0.00422989 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018279 | GGCCATGGGGAGCGC[A/T]GGCAGGAAGCAGGTG | 9051 |
| rs746414249 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999812 | TCCTCTCCCAGGTCC[C/T]CCATCCCCCGCAACC | 9051 |
| rs746472992 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018050 | GAGATGGAGGCAGGA[A/G]GGAGGCTGTTCCCAG | 9051 |
| rs746474817 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023438 | GGAGGTGGAGGTGGT[A/G]CGGCAGGGGCTGCAG | 9051 |
| rs746483433 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028940 | GAGAGCAGACGCCAA[C/G]CCTCACACAACCTTG | 9051 |
| rs746522552 | snp | C/G/T | 4.99316e-05 | 0.00499637 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025274 | TGACCTGGACCCATC[C/G/T]GTTTTGCAGCTCCCT | 9051 |
| rs746533923 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001075 | GGCTGCACAGTTCTC[C/T]AGCTTGTGAATTTGG | 9051 |
| rs746564664 | snp | A/G | 1.66944e-05 | 0.0028891 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031209 | AGAGTTTGACCGGCT[A/G]ACCATTCTCCGCAAC | 9051 |
| rs746613021 | snp | G/T | 3.40217e-05 | 0.00412428 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037190 | GAGGAAGGGCCAGGA[G/T]CCCCTTCGGACCTGC | 9051 |
| rs746635172 | snp | C/G | 1.73126e-05 | 0.00294211 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032503 | GTAGCTCACAGCTCC[C/G]TTCAGGGCAGAGAAG | 9051 |
| rs746666218 | snp | A/G | 1.70618e-05 | 0.00292072 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037120 | GATGGCTGGTGGACT[A/G]TGGAGAGGAACGGGC | 9051 |
| rs746725364 | in-del | -/AA | 1.67489e-05 | 0.00289381 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035972 | CCACCTGTGCCACCT[-/AA]CCCCTGCACCTGAGA | 9051 |
| rs746771536 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017526 | ACCTCCCTGGATCTC[C/T]GTGAGGGGGGGTTTC | 9051 |
| rs746774380 | snp | A/G | 9.98386e-05 | 0.00706465 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995566 | TTTGCCGCGGCAGAC[A/G]CCTGAGGATGATGCC | 9051 |
| rs746791665 | snp | A/C | 0.375 | 0.216506 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035764 | CAGGGGCCAGTGTCC[A/C]CAGAAGGGGAGGGGT | 9051 |
| rs746815327 | in-del | -/C | 3.36383e-05 | 0.00410098 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031172 | ACCTCCCTCCCACTG[-/C]CCCCCAGGCCTTTCA | 9051 |
| rs746827426 | snp | C/T | 7.80153e-05 | 0.00624512 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995508 | GGACGCTGCTGCTGG[C/T]GCCTGGCCCTCCATC | 9051 |
| rs746828604 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015942 | GGACTTGAGCACGGC[A/G]GTCACAGCCTGCAGG | 9051 |
| rs746898326 | snp | A/C | 1.76646e-05 | 0.00297186 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035813 | TTAGCGTCCACAGAG[A/C]CCCTGACCCCCACCC | 9051 |
| rs746948909 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994607 | TAATCTGGAGACTTG[C/T]GGTGGTGGCGGTGGT | 9051 |
| rs746961231 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032000 | CTGTGCTGCATTCTC[A/G]CTGTGACCTTGGGCA | 9051 |
| rs746964576 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022178 | ACTCAGAGAGAATGA[C/T]GACATTGCTGAGGAT | 9051 |
| rs747042572 | snp | A/G | 1.76783e-05 | 0.00297302 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032404 | CCCCCGGTGAGGTCC[A/G]GCTTGCGGACAGCGC | 9051 |
| rs747049225 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031119 | AGCTGTGAATGGGGC[C/G]CAGCCTGGCCGGGCC | 9051 |
| rs747060067 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030915 | ACTCCCGTCCGAGGT[A/C]CCTCTCACTACCCTT | 9051 |
| rs747130710 | snp | C/T | 0.00010072 | 0.00709577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027949 | GCCGCGGCCTTCCCT[C/T]GAGGAGCAGCGCAGG | 9051 |
| rs747139033 | snp | C/G | 3.36089e-05 | 0.00409919 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037036 | ATGCGCTTTCAATCT[C/G]TTGGCCAGAACCCAG | 9051 |
| rs747162582 | snp | C/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993983 | GCAATCCTCCCCAAA[C/G]TGTTTCCTCTTGGGT | 9051 |
| rs747225781 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004959 | ATCCCAATGCCCAGG[A/C]CACACCCCAGGTCAA | 9051 |
| rs747292223 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025956 | GTCACTGGAAACTGG[G/T]CTTGAGTCCAAGGAT | 9051 |
| rs747329040 | snp | C/T | 8.29153e-05 | 0.00643823 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018136 | CATGTGTCCTTCTGT[C/T]CTGTGTCACAGTGCA | 9051 |
| rs747418008 | snp | A/G | 2.32129e-05 | 0.00340674 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030473 | GGAGCTCGTGTCAGG[A/G]CCCTCCCTGAGGCTG | 9051 |
| rs747487700 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025111 | CAGAAATCAGTCTGG[A/G]GCCCCAGTGGATGGT | 9051 |
| rs747497361 | snp | A/G | 1.67618e-05 | 0.00289493 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035984 | ACCTCCCCTGCACCT[A/G]AGAGCTCCCTCTCCC | 9051 |
| rs747547040 | in-del | -/ACAT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000501 | CACACACACACACAC[-/ACAT]ACACACACACACTTT | 9051 |
| rs747711304 | snp | C/G | 0.000152172 | 0.00872141 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035607 | ACACACTGATCCTGG[C/G]GGGGAGGAGAGGTCT | 9051 |
| rs747743285 | snp | C/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036086 | GGCACGTGTGCCCGA[C/G]TGTGTCCACACTAGC | 9051 |
| rs747785719 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012644 | TACTGACTGTAGGGC[A/G]GTGGAAGGAGCCTGG | 9051 |
| rs747789532 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999990 | GTCACATGCACTGCA[A/G]TGACTGTCACCCACC | 9051 |
| rs747874076 | in-del | -/GAGCCAGCA | 6.02246e-05 | 0.00548714 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037215 | CCTGCCCTGCCAGTG[-/GAGCCAGCA]GAGCCAGCAGTGCCC | 9051 |
| rs747910381 | snp | C/T | 9.24684e-05 | 0.00679895 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027923 | CATGGAGGTGAGCGC[C/T]AGGGCCTGGGGCCGC | 9051 |
| rs747927835 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021421 | TTAGGGCCAGGCGCC[A/G]TGCCTCACGCCTATA | 9051 |
| rs747930077 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020268 | TATTCAAGGCCAGGT[C/G]GGGCAGGGTCTGCCC | 9051 |
| rs747963818 | snp | G/T | 0.00014038 | 0.00837678 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027714 | GCAGCAGGCTCTGGG[G/T]GAGGGAGGGCAGCCT | 9051 |
| rs748007237 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020290 | GGTCTGCCCTGACTT[A/G]TCCTTTGTGTGGCCC | 9051 |
| rs748010336 | snp | A/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994495 | CCAAACACCCCACTC[A/T]GTGCCTTGATAATCC | 9051 |
| rs748059282 | snp | C/T | 5.24893e-05 | 0.00512268 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035503 | TCTTTCCTCCCTGTT[C/T]CCAGGTTCTCTGGAC | 9051 |
| rs748088383 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031027 | GGCTGGCCCGGAGTC[A/G]GGATGGGGACCCCAG | 9051 |
| rs748095087 | snp | G/T | 2.30715e-05 | 0.00339635 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995497 | TGCCAGGACTGGGAC[G/T]CTGCTGCTGGCGCCT | 9051 |
| rs748199136 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009599 | CTCAGTTAACATGCA[C/T]GAATCCCCTCGGCTG | 9051 |
| rs748205341 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008157 | CTAAACGCAGCCAGG[C/T]GTGAGGTCTGCACAG | 9051 |
| rs748215230 | snp | A/C/T | 6.15509e-05 | 0.00554728 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032266 | GGGCAGAGTGGGCAT[A/C/T]GGGCTGCGGCCTCTG | 9051 |
| rs748271655 | snp | C/T | 9.24086e-05 | 0.00679675 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018106 | CTGTGCTCAGTGTCG[C/T]CTGGTCGTGGCCCTC | 9051 |
| rs748306987 | snp | C/T | 0.000110733 | 0.00744006 | missense, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035909 | CCAGCCCAGGAGTAC[C/T]GGGCGCTCTACGATT | 9051 |
| rs748312884 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003945 | ATAGGGTGAGCCTTA[A/T]ACATAGATCTTGCTG | 9051 |
| rs748368596 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025790 | GGCAGAGGCCTGGCC[A/G]CTGGCACTAAGGCCA | 9051 |
| rs748502079 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997754 | AAGAAAATCAGACAA[A/G]GTGGCTAGAACAATA | 9051 |
| rs748508648 | in-del | -/CTC | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036057 | ATCTTCGAGCATCCT[-/CTC]CTCCTCAGGAGGGCA | 9051 |
| rs748514164 | snp | C/T | 3.47826e-05 | 0.00417014 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032841 | GGGGCCGCCCTGGGG[C/T]TCACGGCTTGCTGTC | 9051 |
| rs748609098 | snp | C/T | 0.000182932 | 0.00956205 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007970 | CTCCTGAACAATTGC[C/T]CATTGACCTGGACCA | 9051 |
| rs748633983 | snp | C/G | 4.76644e-05 | 0.00488159 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030465 | GGGGTGGAGGAGCTC[C/G]TGTCAGGGCCCTCCC | 9051 |
| rs748640369 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033299 | TGTCTGGCTGGAGCA[C/G]GACTGGGGCATCTGG | 9051 |
| rs748670329 | snp | A/G | 0.000716931 | 0.0189196 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007854 | CCGTCTAGGCCTCCC[A/G]AAGTGCTGGGATTAC | 9051 |
| rs748672214 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018788 | CAGTCATTTGCAGCG[A/C]AGTCTGCACCAGCCT | 9051 |
| rs748770246 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035033 | GAGGCCTCAGCAGGG[C/T]ACGTGAGCCAGGCTT | 9051 |
| rs748783442 | snp | A/G | 6.51247e-05 | 0.00570597 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030484 | CAGGGCCCTCCCTGA[A/G]GCTGCCTGCGCTTTC | 9051 |
| rs748788047 | snp | A/T | 3.67006e-05 | 0.00428357 | intron-variant, synonymous-codon, stop-gained, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032947 | GTCCTGCGGCATGAT[A/T]AAGAGGTGAGGCCCC | 9051 |
| rs748817883 | snp | C/T | 5.55386e-05 | 0.00526936 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035486 | GGCGGGGACACTCAC[C/T]CTCTTTCCTCCCTGT | 9051 |
| rs748852205 | in-del | -/CA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036783 | ACCCCTGACATGCTC[-/CA]GTCACTGCGTCTCCA | 9051 |
| rs748886169 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009889 | GTAGGTGGTGTGGGA[A/G]GGCAATGCCTGGGGA | 9051 |
| rs749041160 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030245 | CCAGAGATGCCCAGA[A/G]GCCAATACTCTGGAC | 9051 |
| rs749074627 | in-del | -/GGG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020869 | ATCTTAGACTCCTGT[-/GGG]GGGGGGGGGTGTGTG | 9051 |
| rs749077664 | snp | A/G | 1.70165e-05 | 0.00291684 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032335 | CGCTGGAAGGCTGCA[A/G]CATAGACGCCGACAT | 9051 |
| rs749139426 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004582 | ACAGTGGCCAGGCGT[C/G]GTGGCTCACACCTGT | 9051 |
| rs749158155 | snp | C/G | 5.0176e-05 | 0.00500854 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031327 | AGGGCAGCCTCTAGG[C/G]AGCAAAGCACCCAGG | 9051 |
| rs749199585 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029351 | CTCTTTCCATGGAGC[C/T]AGCCTGTGGTCCTCT | 9051 |
| rs749226896 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003773 | AACCTCAGTTTCCTC[A/C]TCTGCAGGATGTCAG | 9051 |
| rs749278933 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024593 | TCCGTTTTAAATACT[A/G]CAAGGGGCATACTAT | 9051 |
| rs749330840 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013986 | CCCCAGCTGAGGGAA[A/G]GTGTTTCTGGTCGGG | 9051 |
| rs749404844 | snp | A/G | 1.65899e-05 | 0.00288005 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995588 | GATGATGCCCCAGCT[A/G]CAGTTCAAAGATGCC | 9051 |
| rs749462900 | snp | C/G | 1.95181e-05 | 0.00312389 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035888 | ATACAGGGAAACCCG[C/G]CCTCACCAGCCCAGG | 9051 |
| rs749494132 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023390 | GCACCTGGAAGCAAC[A/G]GGCGGAGGGGCAGAG | 9051 |
| rs749506717 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996495 | GCTGCCTCCAACCCC[A/G]AAGAGGACGCTCTGG | 9051 |
| rs749507706 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033882 | GGAGGCAGCACACCC[A/G]CAGCCTCACATGCTA | 9051 |
| rs749666299 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007200 | GCTCTCACTCTTCTT[C/T]AAGGAGGGTCTGGAG | 9051 |
| rs749738192 | snp | A/C | 0.000117199 | 0.00765413 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032830 | ATGGGGTGTTGGGGG[A/C]CGCCCTGGGGCTCAC | 9051 |
| rs749747350 | snp | A/G | 0.000181332 | 0.00952014 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028615 | AGCAGGCCTTCGAGC[A/G]CATTAGCGCCAACGG | 9051 |
| rs749862420 | in-del | -/CC | 4.69517e-05 | 0.00484496 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028547 | TCACGCCCCTCCACA[-/CC]CCCAGTCCAAGAAGA | 9051 |
| rs749871374 | snp | A/G | 1.69859e-05 | 0.00291421 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032374 | TCATCCAGGCCAAGA[A/G]CACGGGCACAGAGCC | 9051 |
| rs749881993 | snp | A/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994342 | TCCAGAAATATTCTC[A/G]ACACCGTCTACTTTC | 9051 |
| rs749932813 | snp | A/G | 1.6888e-05 | 0.00290581 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037015 | CCTGCAGGCCCTTCC[A/G]ACGTCATGCGCTTTC | 9051 |
| rs749971627 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005613 | CTTCATCATCCTGAA[C/G]AGAAATTGTACCCAT | 9051 |
| rs750011080 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996955 | CTGGAAACCCAGGCC[-/A]CTCTGTAGCCCAGGG | 9051 |
| rs750011720 | snp | A/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993402 | CCCTGGCTGGACAGG[A/T]ACAGTTGGGAAAGGA | 9051 |
| rs750156022 | snp | A/G | 4.25071e-05 | 0.00460996 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995382 | CCCCAAACAAAACAG[A/G]TTGAGCTTTTTCCTC | 9051 |
| rs750160336 | snp | A/C | 0.000172414 | 0.00928317 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027870 | GAGGCCGTCATGGAC[A/C]GGGTCCAGAAGAGCA | 9051 |
| rs750181910 | snp | A/C | 1.92369e-05 | 0.0031013 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035885 | GAGATACAGGGAAAC[A/C]CGGCCTCACCAGCCC | 9051 |
| rs750291257 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014663 | GAAAAGGGGGAAGTG[G/T]CGGTAGTTACAGAGG | 9051 |
| rs750318154 | snp | A/G | 2.99702e-05 | 0.00387094 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035939 | TATACAGCGCAGGTG[A/G]GGCCTCTATACCCCA | 9051 |
| rs750445188 | snp | A/G | 3.33422e-05 | 0.00408289 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018194 | AGGTGCTGCTGCAGC[A/G]GCTTCTGGATGGCAG | 9051 |
| rs750510893 | snp | C/T | 1.6649e-05 | 0.00288518 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025339 | TCCCCTACCCTGGGG[C/T]AATGGGATCTTTTGG | 9051 |
| rs750516188 | snp | A/G | 6.0098e-05 | 0.00548137 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037216 | CCTGCCCTGCCAGTG[A/G]AGCCAGCAGTGCCCC | 9051 |
| rs750526205 | snp | C/T | 3.76187e-05 | 0.00433681 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032592 | CTAAGGGCATGATGG[C/T]ACTCAGAGGAAGAGG | 9051 |
| rs750545421 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008629 | TGACCAGGCTTGTCT[C/T]GCACTCCTGACCTCA | 9051 |
| rs750572947 | snp | A/G | 0.000233859 | 0.0108109 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037147 | GGGCAGCGTGGCTTC[A/G]TCCCTGGTTCCTACC | 9051 |
| rs750598433 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018408 | AACCTGGGCCTCCCC[C/G]AGAGGTGGCAAGTCA | 9051 |
| rs750599218 | snp | A/G | 1.9025e-05 | 0.00308417 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028701 | AGGGCTGGGGGCAGT[A/G]GGGGAGGCAAGGAAG | 9051 |
| rs750616270 | snp | G/T | 3.66858e-05 | 0.0042827 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032896 | CTATTACGATCGGGA[G/T]GTCACCCCGCTGACC | 9051 |
| rs750667964 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008247 | ACCCTGAAACCAAAG[-/A]AACAGGTGTGGCTGG | 9051 |
| rs750810720 | snp | A/G | 3.97757e-05 | 0.0044594 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030620 | GTTTTCCCCAGCTGG[A/G]AAGTGTGAGACGCCC | 9051 |
| rs750823506 | snp | A/G | 0.00012472 | 0.00789587 | synonymous-codon, nc-transcript-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035803 | CACCCTGCTCTTAGC[A/G]TCCACAGAGACCCTG | 9051 |
| rs750827455 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030713 | ACTCGTTTATTCAGC[C/T]TCCTGCTCACAGGCC | 9051 |
| rs750868747 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001739 | GCAGTGCACCTGGTC[A/G]GCAACCCGTTGTGAA | 9051 |
| rs750921765 | in-del | -/TCCCTCCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024727 | GCAGTGCTGGGCCCT[-/TCCCTCCC]TCCCTCCCTCCCTCC | 9051 |
| rs750960050 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023010 | GGGACAGAGGCTGAA[C/T]GTCCACCTGGCAGTG | 9051 |
| rs750976455 | in-del | -/CTATGGAGCCAGGC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996595 | CCAGGAGGATGAGAG[-/CTATGGAGCCAGGC]CTTCCTTCCCTTCCG | 9051 |
| rs750990216 | snp | C/G | 1.66468e-05 | 0.00288498 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025251 | TTCCCGCTGTGCTCT[C/G]CTCCTCCTGACCTGG | 9051 |
| rs751070867 | snp | C/T | 0.000162061 | 0.00900025 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015938 | CTGGGGACTTGAGCA[C/T]GGCGGTCACAGCCTG | 9051 |
| rs751107350 | snp | G/T | 1.66935e-05 | 0.00288903 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031302 | TGAGGGCCTTGGTGT[G/T]GGGTAAGGTAGGGCA | 9051 |
| rs751120496 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003425 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATCTGAG | 9051 |
| rs751147841 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028379 | ACTACCAGCAGCCCC[A/C]ACGCCTTCTCTATCT | 9051 |
| rs751218366 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037260 | ACCTTGCTAGGGCCC[A/G]GAACCAAGCGTCCCC | 9051 |
| rs751258634 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024208 | CTGAGAATCTGTATT[A/T]CTAACAGGCTCCGCG | 9051 |
| rs751280536 | snp | C/T | 1.84123e-05 | 0.00303411 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028680 | GCTGGGCCGTGTGGG[C/T]CGCCCAGGGCTGGGG | 9051 |
| rs751331706 | snp | C/G | 4.25867e-05 | 0.00461428 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032544 | GGTTGTGGGGAGTTG[C/G]GTCCCAGGCCTGCTG | 9051 |
| rs751343112 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998282 | CATGTTTGATATCAC[A/C]GCCCCTCAGTTATTG | 9051 |
| rs751348240 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023141 | CCATGAACCGGGGTG[A/G]CCCACAGGTGGGTTT | 9051 |
| rs751419563 | in-del | -/GT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020882 | GTGGGGGGGGGGGGT[-/GT]GTGTGTTGGCCCTCA | 9051 |
| rs751436702 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008425 | TTGTTTTGTTTGTTT[G/T]TTGAGACAGAGTCCC | 9051 |
| rs751453867 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996250 | ATTCAACACGGGCTT[A/C]AATCAAGTCATTTCC | 9051 |
| rs751519484 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005983 | AAACCCTGCTTTCAA[C/T]TCTTTTAGATTATAC | 9051 |
| rs751519871 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998160 | GGAGAACAGCTTGAA[-/C]CCAAGAGGCAGAGGT | 9051 |
| rs751528698 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006880 | AATCAAGAAGTGTGA[G/T]TCCTCCAAACTTATT | 9051 |
| rs751528894 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018359 | ACTCTGTCAGAACAC[A/G]CCCTGCTTTAAAAAA | 9051 |
| rs751553131 | snp | A/G | 6.62888e-05 | 0.00575674 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995649 | TGAACAAGTGGAGGG[A/G]GCAGAGCTAGGCTGA | 9051 |
| rs751570626 | snp | A/C | 3.43802e-05 | 0.00414595 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029594 | GTGGGCCTGGCTGCC[A/C]CGTCCGACCAGGGCG | 9051 |
| rs751587689 | in-del | -/TGA | 3.42924e-05 | 0.00414065 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018425 | GAGGTGGCAAGTCAC[-/TGA]TGATCTTTCAAATGC | 9051 |
| rs751601401 | in-del | -/GATG | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037746 | AAACAGGAAGCTGGT[-/GATG]GATCTGTTGGAGAGG | 9051 |
| rs751618284 | snp | A/G | 6.13779e-05 | 0.00553942 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018474 | CCCAGGCGGAGGAGC[A/G]GTACGGGAAGGAGCT | 9051 |
| rs751643479 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998178 | AAGAGGCAGAGGTTG[C/T]AGTGAGCTGAGATTG | 9051 |
| rs751668240 | snp | C/T | 3.34627e-05 | 0.00409026 | stop-gained, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031192 | CAGGCCTTTCAGCTG[C/T]AAGAGTTTGACCGGC | 9051 |
| rs751682755 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017454 | CCCCAGTCCAGAGGT[A/G]AATGTAGGGTGTGCT | 9051 |
| rs751688277 | snp | A/G | 1.68069e-05 | 0.00289882 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037089 | AGACATCCTGGAGGT[A/G]ATCCTGGAAGGGGAG | 9051 |
| rs751722651 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027430 | CCTGTGATCATGCGT[A/G]TGGGCAGCTAGGGAT | 9051 |
| rs751754970 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036411 | GGAAAACTGTGGCCA[A/G]AATGAGTCTTGCTAT | 9051 |
| rs751761730 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001556 | CTTGCAGACAGTGCA[A/G]GAGGTGGGAGAGAGA | 9051 |
| rs751854381 | in-del | -/CACAGGGTGGCAGGGCAGCA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026342 | GAGGGTGGTGCCCTG[-/CACAGGGTGGCAGGGCAGCA]CACAGATCCGCTTCT | 9051 |
| rs751889307 | snp | A/G/T | 1.77068e-05 | 0.00297541 | missense, stop-gained, nc-transcript-variant, splice-acceptor-variant | PSTPIP1 | GRCh38.p7 | 15:77035810 | CTCTTAGCGTCCACA[A/G/T]AGACCCTGACCCCCA | 9051 |
| rs751889923 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019666 | GCCTAGCCTCTCCAA[G/T]TTTGTTTCTCACCTC | 9051 |
| rs751915664 | snp | A/G | 6.08106e-05 | 0.00551376 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035577 | TGGTAAAGGGGGTCA[A/G]GAGGGGACCCCCAAA | 9051 |
| rs751927068 | snp | A/G | 1.6838e-05 | 0.0029015 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995544 | AGCCTGTGGCAGGAG[A/G]GTGAGCTTTGCCGCG | 9051 |
| rs751980031 | snp | A/G | 4.85543e-05 | 0.00492695 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995466 | GCCGGCCGGGAAGGG[A/G]GGCCTGGGCCAGCCC | 9051 |
| rs751991713 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011818 | GGGCGCTCCTCACCT[A/G]TCAAAGCCCCCCACC | 9051 |
| rs752005551 | snp | C/G | 1.85424e-05 | 0.00304481 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030600 | AGTGGCCCACGTGGA[C/G]CCTCGTTTTCCCCAG | 9051 |
| rs752065101 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031583 | GGAGGGGAGGTGGAC[A/G]CAGCTGTCAGAGGTT | 9051 |
| rs752123803 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995624 | GGTGAGTGAGGATGG[C/T]TGGGGGCACTGAACA | 9051 |
| rs752204736 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008633 | CAGGCTTGTCTCGCA[C/T]TCCTGACCTCAGGTA | 9051 |
| rs752232834 | snp | A/C | 8.45773e-05 | 0.00650242 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028656 | CAGGTGGAGAAGGTG[A/C]GCTGGGCTGCTGGGC | 9051 |
| rs752253878 | snp | C/T | 1.77413e-05 | 0.00297831 | missense, nc-transcript-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035808 | TGCTCTTAGCGTCCA[C/T]AGAGACCCTGACCCC | 9051 |
| rs752256108 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031799 | GATGCAGCCCAGCAC[A/T]CGGCTCTCCCGGGCA | 9051 |
| rs752373915 | in-del | -/GG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020870 | TCTTAGACTCCTGTG[-/GG]GGGGGGGGGTGTGTG | 9051 |
| rs752385734 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023073 | TGGGGGCTGGGAAAA[A/G]GGCCAGCAGCTCCCA | 9051 |
| rs752402033 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032717 | GGTACCTACGGTGGG[C/G]TCTCTCATGGGAGCA | 9051 |
| rs752420721 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034145 | GCAGGACTGGGAAGA[-/G]GGCGGGGGTCAGTGA | 9051 |
| rs752461869 | snp | C/T | 2.72216e-05 | 0.00368918 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032453 | GCCCCTGGGAAGGCC[C/T]GGCCCTGAGCCTCAA | 9051 |
| rs752462668 | snp | A/G | 5.03833e-05 | 0.00501888 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037083 | CGCGGGAGACATCCT[A/G]GAGGTGATCCTGGAA | 9051 |
| rs752518482 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022461 | GTGACAGATGGCAGT[A/G]GGCAGAGGCCTGTGC | 9051 |
| rs752558971 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017196 | GGCCCCGGGACCCAC[-/T]CCCCAAGCCTGGGAA | 9051 |
| rs752570265 | snp | G/T | 7.57088e-05 | 0.00615213 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028578 | ACATACGAGCAGAAG[G/T]GCCGGGACGCGGACG | 9051 |
| rs752592083 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006147 | TTCTGTTTTTTTTTT[-/A]AATCATAGCCACCTT | 9051 |
| rs752624664 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005962 | TGGTGTACAAGTACC[C/T]GTTTGAAACCCTGCT | 9051 |
| rs752689698 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034860 | TTTCCTTTATTCAGT[A/G]AACCTTCATGACCCC | 9051 |
| rs752714806 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016316 | TGCAGGAGGCTGAGG[C/T]CCCAGATTTGTTTTT | 9051 |
| rs752786501 | snp | C/T | 1.84116e-05 | 0.00303405 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030594 | GAGGTGAGTGGCCCA[C/T]GTGGAGCCTCGTTTT | 9051 |
| rs752804181 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999445 | CGCCACGTCTGTCTA[A/C]TTTTTGTATTTTTAG | 9051 |
| rs752827809 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026627 | CAGACAGGGCTCCAG[C/G]TCTGGTTAGCAGCTC | 9051 |
| rs752909805 | in-del | -/GTC | 7.28146e-05 | 0.00603341 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033003 | TGGGCCAGGAAGTGG[-/GTC]GAGCCCCTCCTCTGC | 9051 |
| rs752936181 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034704 | TAGTAAAGCTTCACT[C/G]ATCTTTGAAGACTCA | 9051 |
| rs752997807 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010335 | CTGGAGGGGATCATG[A/C]GTGAGAGCCCCACCA | 9051 |
| rs753015326 | in-del | -/AGAG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034037 | GCCCCAGAGAGGATT[-/AGAG]AGAGAGAGAGAGAGA | 9051 |
| rs753026268 | snp | A/G | 3.35576e-05 | 0.00409606 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018464 | TTTTGCAGGGCCCAG[A/G]CGGAGGAGCGGTACG | 9051 |
| rs753081335 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032963 | AAGAGGTGAGGCCCC[C/G]ACAGACGGAGGGAGG | 9051 |
| rs753082701 | snp | C/T | 4.72088e-05 | 0.00485821 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995368 | GCTGCTGATTCTAGC[C/T]CCAAACAAAACAGGT | 9051 |
| rs753139065 | snp | C/T | 0.000117062 | 0.00764965 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025644 | GAGCTGCTCCCCCAT[C/T]GCCAGCCTCTCAGTT | 9051 |
| rs753143073 | in-del | -/CAG | 6.65818e-05 | 0.00576944 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025263 | CTCCTCCTCCTGACC[-/CAG]TGGACCCATCTGTTT | 9051 |
| rs753152247 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020739 | GAAGCCCTCCCAGAC[A/G]CCTTGCCTTGCCTTA | 9051 |
| rs753207002 | snp | A/G | 0.000192697 | 0.00981383 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995458 | CAGACGGCGCCGGCC[A/G]GGAAGGGGGGCCTGG | 9051 |
| rs753366207 | snp | C/T | 6.59e-05 | 0.00573983 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035589 | TCAGGAGGGGACCCC[C/T]AAACACACTGATCCT | 9051 |
| rs753370729 | snp | C/T | 3.04419e-05 | 0.00390128 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995482 | GGCCTGGGCCAGCCC[C/T]GCCAGGACTGGGACG | 9051 |
| rs753419917 | snp | A/G | 1.70307e-05 | 0.00291806 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027880 | TGGACCGGGTCCAGA[A/G]GAGCAAGCTGTCGCT | 9051 |
| rs753457528 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995702 | TGCGGCTCCGAGAGG[A/G]GAGCTTTCTCATAAA | 9051 |
| rs753473855 | snp | A/C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006699 | GCCATTTGTTGAAGT[A/C/T]TGTCCTTTTCTCATA | 9051 |
| rs753475851 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994467 | AACAAAAACTGGGCC[C/T]CAGACTGGGTTTCCA | 9051 |
| rs753501213 | snp | A/G | 1.6784e-05 | 0.00289685 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995547 | CTGTGGCAGGAGAGT[A/G]AGCTTTGCCGCGGCA | 9051 |
| rs753672012 | snp | G/T | 3.03845e-05 | 0.00389761 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035941 | TACAGCGCAGGTGAG[G/T]CCTCTATACCCCAAA | 9051 |
| rs753691479 | snp | A/G | 1.6953e-05 | 0.0029114 | splice-donor-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018249 | GCTACTGAGGCAGAG[A/G]TGAGCTGCTGGGCAG | 9051 |
| rs753802611 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035409 | CAGCCCTGGCAGAGC[A/G]CGTGCAGCTCTGAGA | 9051 |
| rs753855992 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034639 | TCCTCCCCTGCACCT[A/G]AGCCCTCCCTCTCCT | 9051 |
| rs753889391 | snp | A/G | 9.74073e-05 | 0.00697812 | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032913 | TCACCCCGCTGACCA[A/G]CAGCCCTGGCATACA | 9051 |
| rs753925976 | snp | A/C/G | 6.17608e-05 | 0.00555667 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032986 | GAGGGAGGGCCTAAG[A/C/G]CTGGGCCAGGAAGTG | 9051 |
| rs753932071 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999424 | GCTGGGATTACAGAC[A/G]TGCGCCGCCACGTCT | 9051 |
| rs753934590 | snp | A/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998577 | GGCAGTCTGCACAGT[A/T]CCTGATATACAGTTG | 9051 |
| rs753941356 | snp | A/G | 0.000103194 | 0.00718236 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029619 | AGGGCGGAGGCCTGG[A/G]CGGTACTCCCCACAC | 9051 |
| rs754018655 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010144 | CTTGCCCTCACTGTC[A/G]GCCTCCTTCCTCGCC | 9051 |
| rs754171160 | snp | A/T | 0.00017301 | 0.00929921 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016033 | TCCACTCTGGGGGCC[A/T]CCATAAGGACAGGAG | 9051 |
| rs754175237 | snp | A/G | 1.78733e-05 | 0.00298937 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030517 | AGCGGGTATACAGGC[A/G]GAGCATTGCGCAGCT | 9051 |
| rs754211064 | snp | C/T | 1.6659e-05 | 0.00288604 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025357 | TGGGATCTTTTGGGA[C/T]TGCGAGGCTGGTGGA | 9051 |
| rs754304151 | snp | A/G | 6.20367e-05 | 0.00556906 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018504 | TGGTGCAGATCGCAC[A/G]GAAGGCAGGTGGCCA | 9051 |
| rs754306026 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029691 | CACAATCATGGGCGC[A/G]GCGCTCTCATTCCAG | 9051 |
| rs754321842 | snp | A/G | 3.68521e-05 | 0.0042924 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037139 | AGAGGAACGGGCAGC[A/G]TGGCTTCGTCCCTGG | 9051 |
| rs754358552 | snp | A/G | 0.000211954 | 0.0102923 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025625 | GCAGGTGCAGGGGGC[A/G]GGGGAGCTGCTCCCC | 9051 |
| rs754365662 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001786 | ATTTATACTGGCGCA[G/T]GCTTGTAGTATTAAC | 9051 |
| rs754421229 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012506 | ATCCACCCACCCATC[A/C]ATCCATCCTTCCATC | 9051 |
| rs754487450 | snp | A/G | 2.73004e-05 | 0.00369452 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995486 | TGGGCCAGCCCTGCC[A/G]GGACTGGGACGCTGC | 9051 |
| rs754491298 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003634 | GCACTCCAGCCTGGG[C/T]AAAAGAACGAAACTC | 9051 |
| rs754499321 | snp | C/T | 6.68505e-05 | 0.00578107 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995556 | GAGAGTGAGCTTTGC[C/T]GCGGCAGACGCCTGA | 9051 |
| rs754506783 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021905 | CTATTGCTCATCCTG[C/T]GTCAGGTAAGGTGCT | 9051 |
| rs754508419 | snp | C/T | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036047 | GGTTTCACTCATCTT[C/T]GAGCATCCTCTCCTC | 9051 |
| rs754566975 | snp | C/G | 1.77925e-05 | 0.0029826 | missense, nc-transcript-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035805 | CCCTGCTCTTAGCGT[C/G]CACAGAGACCCTGAC | 9051 |
| rs754666881 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021264 | GAGGTTACATCTTAA[G/T]TGATTTTTGACATGT | 9051 |
| rs754691023 | snp | C/G | 1.73039e-05 | 0.00294137 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035603 | CCAAACACACTGATC[C/G]TGGGGGGGAGGAGAG | 9051 |
| rs754872550 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017786 | ATATTGGAAGGGTGG[C/T]ACTGTGAGTGAGTGA | 9051 |
| rs754924944 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016294 | TGCTGGTGTCCCTCC[A/G]GGCAGGTGCAGGAGG | 9051 |
| rs754947098 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004597 | GGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG | 9051 |
| rs754956530 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025712 | AGTGGAGGGCGGCAG[G/T]GGTGGTGGTGGGACA | 9051 |
| rs755053996 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034667 | CCTGGTCACCTGCAG[C/T]GCCTCGCTCCCCCTT | 9051 |
| rs755116964 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024810 | TGCTAGCCTCTCCCA[C/T]GGCCATCCAACCTCC | 9051 |
| rs755159236 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998503 | TGAACTCTAATTTCA[C/T]CCACAATTTTAATGA | 9051 |
| rs755168700 | snp | C/T | 9.81178e-05 | 0.00700352 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035950 | GGTGAGGCCTCTATA[C/T]CCCAAACCCACCTGT | 9051 |
| rs755179880 | snp | C/T | 0.000104652 | 0.00723291 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029620 | GGGCGGAGGCCTGGG[C/T]GGTACTCCCCACACA | 9051 |
| rs755212769 | snp | A/G | 6.74787e-05 | 0.00580816 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018251 | TACTGAGGCAGAGGT[A/G]AGCTGCTGGGCAGGC | 9051 |
| rs755230675 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008753 | GGCTGAGAGTAAAAC[A/G]TTAAATAGTGAGTGG | 9051 |
| rs755250484 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034001 | CACCTGAAGCAGTAT[C/T]AGGAAGGGGCAGAAA | 9051 |
| rs755267763 | snp | A/G | 1.77659e-05 | 0.00298038 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030520 | GGGTATACAGGCAGA[A/G]CATTGCGCAGCTGGA | 9051 |
| rs755268431 | in-del | -/T | 0.00789624 | 0.0623359 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018445 | ATCTTTCAAATGCCC[-/T]TTTTTTTGCAGGGCC | 9051 |
| rs755286625 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009218 | CCTCAGGCTCAGCTC[C/T]GAGGCCCTGAACCTG | 9051 |
| rs755363123 | snp | C/T | 1.66671e-05 | 0.00288674 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025360 | GATCTTTTGGGACTG[C/T]GAGGCTGGTGGAGGG | 9051 |
| rs755491182 | snp | C/T | 6.41869e-05 | 0.00566474 | intron-variant, synonymous-codon, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032920 | GCTGACCAGCAGCCC[C/T]GGCATACAGCCGTCC | 9051 |
| rs755585435 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028865 | ATCCCCTTTGCCACC[A/G]TCAGGCGGCACTCAG | 9051 |
| rs755790871 | snp | C/G | 4.6435e-05 | 0.00481823 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995468 | CGGCCGGGAAGGGGG[C/G]CCTGGGCCAGCCCTG | 9051 |
| rs755802079 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030479 | CGTGTCAGGGCCCTC[C/T]CTGAGGCTGCCTGCG | 9051 |
| rs755806301 | snp | A/G | 3.40512e-05 | 0.00412607 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027871 | AGGCCGTCATGGACC[A/G]GGTCCAGAAGAGCAA | 9051 |
| rs755840747 | snp | C/T | 3.85564e-05 | 0.00439053 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035886 | AGATACAGGGAAACC[C/T]GGCCTCACCAGCCCA | 9051 |
| rs755846915 | snp | C/G | 4.07456e-05 | 0.00451344 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995388 | ACAAAACAGGTTGAG[C/G]TTTTTCCTCCCCTCA | 9051 |
| rs755903781 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003752 | GAGAATCATTTTCCC[C/T]TTCTGAACCTCAGTT | 9051 |
| rs755980692 | snp | A/G | 0.000161852 | 0.00899442 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015985 | TTTCTGACTCCTCCC[A/G]AATGGCCAGCGTAGG | 9051 |
| rs756046377 | snp | C/T | | | intron-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77024528 | TAAAATACTGGATGC[C/T]CAGGTGAACGTGAAT | 9051 |
| rs756061977 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998437 | GAGCTTTCCTTAAAG[C/T]TCATATACTACACTC | 9051 |
| rs756068066 | snp | A/C/G | 0.000120252 | 0.00775334 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035940 | ATACAGCGCAGGTGA[A/C/G]GCCTCTATACCCCAA | 9051 |
| rs756098756 | in-del | -/AC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024593 | TCCGTTTTAAATACT[-/AC]AAGGGGCATACTATA | 9051 |
| rs756107966 | snp | C/G | 0.00233526 | 0.0340907 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031315 | GTGGGGTAAGGTAGG[C/G]CAGCCTCTAGGCAGC | 9051 |
| rs756126717 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033854 | TGAGAATCTTGTGCA[A/G]GCAGTGACCCCAGGA | 9051 |
| rs756243465 | snp | C/G | 0.000847817 | 0.0205716 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007843 | TCGTGATCTGCCCGT[C/G]TAGGCCTCCCAAAGT | 9051 |
| rs756250919 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033136 | GCCTATGGAACCCTC[A/G]GCCCAAGGGACCCAG | 9051 |
| rs756287775 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034911 | CTGGTGCAGGGGCAG[A/G]GGTAAAGTAGCCCAG | 9051 |
| rs756288702 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033036 | ACCTGGCCCTTCCTC[A/G]TTCACTGAGCACCTA | 9051 |
| rs756355568 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007149 | CTCCCCAAGAAGGTC[A/C]ATCTATGACATCTCG | 9051 |
| rs756356579 | snp | A/G | 8.97868e-05 | 0.00669965 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029600 | CTGGCTGCCCCGTCC[A/G]ACCAGGGCGGAGGCC | 9051 |
| rs756389413 | in-del | -/CT | 5.36495e-05 | 0.00517898 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035498 | CACCCTCTTTCCTCC[-/CT]GTTCCCAGGTTCTCT | 9051 |
| rs756411737 | snp | C/T | 6.8451e-05 | 0.00584985 | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032904 | ATCGGGAGGTCACCC[C/T]GCTGACCAGCAGCCC | 9051 |
| rs756411858 | snp | A/G | 8.75695e-05 | 0.00661643 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029490 | GGGCCCTGGCTCCTG[A/G]GGCAGGGGCTTAGCG | 9051 |
| rs756426938 | snp | C/T | 6.43232e-05 | 0.00567075 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018465 | TTTGCAGGGCCCAGG[C/T]GGAGGAGCGGTACGG | 9051 |
| rs756479369 | in-del | -/A | 4.93644e-05 | 0.00496787 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025465 | CCCATCAGATCTGAC[-/A]ACTGGGGACCAGTAT | 9051 |
| rs756502979 | snp | A/G | 1.67195e-05 | 0.00289127 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031196 | CCTTTCAGCTGCAAG[A/G]GTTTGACCGGCTGAC | 9051 |
| rs756577454 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027644 | AGCAAGGACCTCACG[G/T]CACACCCATGCCCTG | 9051 |
| rs756621016 | snp | C/G | 1.99031e-05 | 0.00315454 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037150 | CAGCGTGGCTTCGTC[C/G]CTGGTTCCTACCTGG | 9051 |
| rs756631956 | snp | G/T | 1.66466e-05 | 0.00288496 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025256 | GCTGTGCTCTCCTCC[G/T]CCTGACCTGGACCCA | 9051 |
| rs756705059 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000890 | ATTTTAAATTGTAGC[A/G]AAATACACATAAAAT | 9051 |
| rs756742999 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036583 | GCACCCCCACATAGC[C/T]AGGCAGGCTGGGTGT | 9051 |
| rs756746823 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004519 | TGCCTGCGTGGCTAG[A/G]GAGAGTGACCAAGGT | 9051 |
| rs756882164 | snp | A/G | 1.66983e-05 | 0.00288944 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031304 | AGGGCCTTGGTGTGG[A/G]GTAAGGTAGGGCAGC | 9051 |
| rs756920835 | snp | C/G | 0.00018558 | 0.00963098 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026101 | CATCCAAAGGTACTT[C/G]TCACCCATATGTAGG | 9051 |
| rs756923227 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014618 | GGTGTCTGTGGTCTC[A/G]CCCCTGCAGCCACCA | 9051 |
| rs756956715 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037265 | GCTAGGGCCCAGAAC[A/C]AAGCGTCCCCCAGCC | 9051 |
| rs757057358 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024262 | GACCTCACTTTGGGA[C/T]CCACGAGTTTAGGGC | 9051 |
| rs757123504 | snp | C/T | 5.53062e-05 | 0.00525833 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035874 | TCGCAGTGCAGGAGA[C/T]ACAGGGAAACCCGGC | 9051 |
| rs757141756 | snp | C/T | 1.84599e-05 | 0.00303803 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028681 | CTGGGCCGTGTGGGT[C/T]GCCCAGGGCTGGGGG | 9051 |
| rs757146479 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999071 | GCGCTGGGAAGCCCA[G/T]AGAAGGAAGGGTCCT | 9051 |
| rs757147257 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023175 | GTTGAGAAAATTTAG[A/G]TTATGAGCCTGGGGA | 9051 |
| rs757184398 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997344 | CCTCTCACACTGAGT[C/T]TGGGCCGATGCCCCG | 9051 |
| rs757195808 | snp | A/G | 4.9717e-05 | 0.00498558 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995655 | AGTGGAGGGGGCAGA[A/G]CTAGGCTGAAATCTC | 9051 |
| rs757195838 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022904 | AGGTAGCACCAGTAT[C/T]TATGCAGTACCCAAG | 9051 |
| rs757237581 | snp | A/C | 1.76602e-05 | 0.0029715 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035814 | TAGCGTCCACAGAGA[A/C]CCTGACCCCCACCCC | 9051 |
| rs757257145 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007026 | GACTGGCCACGAGTC[C/T]GTGACAAACTCCTCA | 9051 |
| rs757324764 | snp | C/T | | | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032925 | CCAGCAGCCCTGGCA[C/T]ACAGCCGTCCTGCGG | 9051 |
| rs757398558 | snp | C/T | 7.57088e-05 | 0.00615213 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028592 | GTGCCGGGACGCGGA[C/T]GACGCGGAGCAGGCC | 9051 |
| rs757428324 | in-del | -/TTG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031884 | TGGGGGTTGATTTTC[-/TTG]TTGTTTTTGCCCAAG | 9051 |
| rs757449886 | snp | A/C | 4.05655e-05 | 0.00450345 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032478 | CCTCAAGTGCCAGGA[A/C]CGGGCTGGGGTAGCT | 9051 |
| rs757476968 | snp | C/T | 5.19359e-05 | 0.00509561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032564 | CAGGCCTGCTGCCTC[C/T]TCTCAGGCAAAGCTA | 9051 |
| rs757507821 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016587 | TGAGCCTGGACCAGG[A/C]CCTCCTCAGGAATTT | 9051 |
| rs757597315 | snp | A/G | | | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035878 | AGTGCAGGAGATACA[A/G]GGAAACCCGGCCTCA | 9051 |
| rs757681032 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011889 | TTTCCTTGCATTGTC[A/C]TGGAGTTGGCCTCCC | 9051 |
| rs757828114 | snp | A/C | 1.67947e-05 | 0.00289777 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037045 | CAATCTCTTGGCCAG[A/C]ACCCAGATGAGCTGG | 9051 |
| rs757841655 | in-del | -/ACCCCC | 1.76216e-05 | 0.00296825 | cds-indel, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035818 | TCCACAGAGACCCTG[-/ACCCCC]ACCCCCACCCCCGAG | 9051 |
| rs757943820 | snp | G/T | 1.65759e-05 | 0.00287883 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995630 | TGAGGATGGTTGGGG[G/T]CACTGAACAAGTGGA | 9051 |
| rs757967257 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013642 | CCACTCAGCTTCTCC[C/T]AGGGGCTCCTCTCTC | 9051 |
| rs758079120 | snp | A/G | 1.66857e-05 | 0.00288835 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031292 | AGGTGGGGGCTGAGG[A/G]CCTTGGTGTGGGGTA | 9051 |
| rs758113705 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012704 | CCTCTGTTTCCGTAT[A/C]TATACAATGGGGATG | 9051 |
| rs758132547 | snp | A/T | 1.79838e-05 | 0.0029986 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035863 | CTACACAGCCATCGC[A/T]GTGCAGGAGATACAG | 9051 |
| rs758138012 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020871 | CTTAGACTCCTGTGG[-/G]GGGGGGGGGTGTGTG | 9051 |
| rs758158079 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022131 | TGTCAGAGAGATTTT[A/T]AAAATTTTTTTCATG | 9051 |
| rs758245509 | snp | A/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994594 | CCCAAACAGCGTCTA[A/G]TCTGGAGACTTGCGG | 9051 |
| rs758258744 | snp | A/G | 0.00018558 | 0.00963098 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027924 | ATGGAGGTGAGCGCC[A/G]GGGCCTGGGGCCGCG | 9051 |
| rs758281034 | snp | C/G/T | 4.99408e-05 | 0.00499683 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995565 | CTTTGCCGCGGCAGA[C/G/T]GCCTGAGGATGATGC | 9051 |
| rs758333224 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006056 | ACTTTTTGAGTAACC[A/G]CCAAACAGTTTTACA | 9051 |
| rs758334058 | snp | C/T | 7.61702e-05 | 0.00617084 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028586 | GCAGAAGTGCCGGGA[C/T]GCGGACGACGCGGAG | 9051 |
| rs758334641 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037379 | TCCTGCTCCAGTGTC[C/T]GAGTGCTCAGTTCAG | 9051 |
| rs758372338 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028188 | AGGGGTGGAGGGAGG[A/C]GGGACCCCTGAGCTT | 9051 |
| rs758382119 | snp | A/G | 7.73425e-05 | 0.00621814 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035609 | ACACTGATCCTGGGG[A/G]GGAGGAGAGGTCTCC | 9051 |
| rs758390838 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035584 | GGGGTCAGGAGGGGA[-/C]CCCCCAAACACACTG | 9051 |
| rs758401072 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996789 | AGCCCAGAGAAGCCA[A/G]TGGAGGCAGAGCTGC | 9051 |
| rs758570337 | snp | A/G | 7.99968e-05 | 0.00632392 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018275 | GGCAGGCCATGGGGA[A/G]CGCAGGCAGGAAGCA | 9051 |
| rs758664536 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034752 | AGCCCTCTTGCCTTG[A/G]AGGCAGTGTCAGCCT | 9051 |
| rs758699821 | snp | A/G | 0.000167232 | 0.00914266 | intron-variant, synonymous-codon, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032932 | CCCTGGCATACAGCC[A/G]TCCTGCGGCATGATA | 9051 |
| rs758707523 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020741 | AGCCCTCCCAGACAC[C/T]TTGCCTTGCCTTACT | 9051 |
| rs758725770 | snp | A/G | 4.60119e-05 | 0.00479623 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995372 | CTGATTCTAGCCCCA[A/G]ACAAAACAGGTTGAG | 9051 |
| rs758855335 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009452 | CCCTATAAGGGCTTA[A/G]GAGTCCACGTATTCT | 9051 |
| rs758856672 | snp | C/T | 2.37459e-05 | 0.00344563 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030466 | GGGTGGAGGAGCTCG[C/T]GTCAGGGCCCTCCCT | 9051 |
| rs758911910 | snp | A/G | 5.27969e-05 | 0.00513767 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030525 | TACAGGCAGAGCATT[A/G]CGCAGCTGGAGAAGG | 9051 |
| rs758916413 | snp | A/C | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993332 | AGGTTCCTCACATTA[A/C]TTCCTTCCCCAGTTG | 9051 |
| rs758926726 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033348 | CCAGGGCTCCTTCCC[C/T]GGCCTGGCTGCAGTC | 9051 |
| rs758952070 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014057 | TTGCTGAACTGCCCC[-/T]GGGTGACAGGCCCTG | 9051 |
| rs758958264 | snp | C/T | 8.39102e-05 | 0.00647673 | splice-donor-variant | PSTPIP1 | GRCh38.p7 | 15:77028654 | AGCAGGTGGAGAAGG[C/T]GCGCTGGGCTGCTGG | 9051 |
| rs758981494 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023016 | GAGGCTGAATGTCCA[C/T]CTGGCAGTGCTGTAC | 9051 |
| rs758981982 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019678 | CAAGTTTGTTTCTCA[C/T]CTCCCACTCCAGCGA | 9051 |
| rs759045973 | snp | C/G/T | 4.97346e-05 | 0.00498651 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995619 | TTTTGGGTGAGTGAG[C/G/T]ATGGTTGGGGGCACT | 9051 |
| rs759214403 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017138 | CTGGAGTAAGCCTGC[A/G]TGCAGTGCCTGGGAG | 9051 |
| rs759326761 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008173 | GTGAGGTCTGCACAG[C/T]ACAGGGAAGCACAGG | 9051 |
| rs759394059 | in-del | -/GCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036947 | CACCCTGGGAGACAT[-/GCC]GCATTTACTGCTGGG | 9051 |
| rs759442242 | snp | A/T | 3.3745e-05 | 0.00410748 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018448 | TTTCAAATGCCCTTT[A/T]TTTTGCAGGGCCCAG | 9051 |
| rs759507050 | snp | A/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036299 | TGGTGCACACGTGCG[A/G]GGAGCTGGCAGAGCC | 9051 |
| rs759520167 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005177 | TCACCTGAGGTCGGG[-/A]GTTCAAGACCAGCCT | 9051 |
| rs759530659 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000271 | AGCCACTGGTGCCTT[C/T]TCCCTTCCCAGTTCT | 9051 |
| rs759583926 | snp | A/G | 3.3761e-05 | 0.00410845 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995454 | GTTGCAGACGGCGCC[A/G]GCCGGGAAGGGGGGC | 9051 |
| rs759587916 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026506 | GTGTCCTGGCCATAC[C/T]ACTTCCCATCTCTGT | 9051 |
| rs759640462 | in-del | -/T | 0.00158181 | 0.0280785 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032848 | CCTGGGGCTCACGGC[-/T]TTGCTGTCTGCAGCT | 9051 |
| rs759648309 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011406 | GCATCTCTGGGACTC[A/G]GCCAGCTGGGCTGCT | 9051 |
| rs759653276 | snp | A/G | 8.74011e-05 | 0.00661006 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995521 | GGCGCCTGGCCCTCC[A/G]TCAGGCCAGCCTGTG | 9051 |
| rs759802964 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010264 | CTCACTTCCTTGTCT[G/T]CCTGTAAGATGGAAC | 9051 |
| rs759806972 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021610 | CTTGAACCTGGGAGA[C/T]GGAGGTTGCAGTGAG | 9051 |
| rs759844248 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005140 | TATAATCCCAGCAGT[C/T]TGGGAGGCCAAGGTG | 9051 |
| rs759881816 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030602 | TGGCCCACGTGGAGC[C/G]TCGTTTTCCCCAGCT | 9051 |
| rs759885135 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015154 | AAATACAGCTTTGAT[A/T]TGAGGTGGAGATAAT | 9051 |
| rs759917096 | snp | A/G | 0.000112682 | 0.00750523 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027814 | GGGGAGCCTCCCGAG[A/G]CCGCGGCCCTCGGCT | 9051 |
| rs759934388 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036622 | CTGATGAGGCCAGGG[C/T]TCGGGGAGGCAGGGA | 9051 |
| rs760005610 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004128 | TACAGAGAGGAAACT[A/G]AGCCTCTTGGAAGGA | 9051 |
| rs760039352 | snp | C/T | 1.69158e-05 | 0.00290819 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037000 | CCCTGCAGGCCCTTC[C/T]CTGCAGGCCCTTCCA | 9051 |
| rs760041282 | snp | C/T | 1.89881e-05 | 0.00308119 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032280 | TCGGGCTGCGGCCTC[C/T]GCTCTTTCCTGCCCC | 9051 |
| rs760064045 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001571 | GGAGGTGGGAGAGAG[A/T]GGCCCTGGCCATCCT | 9051 |
| rs760098436 | snp | A/C | 2.49268e-05 | 0.00353026 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025640 | GGGGGAGCTGCTCCC[A/C]CATTGCCAGCCTCTC | 9051 |
| rs760205701 | snp | A/G | 0.000119772 | 0.00773769 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028562 | CCCCCAGTCCAAGAA[A/G]ACATACGAGCAGAAG | 9051 |
| rs760217354 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006630 | TTTTTGCATATGGTA[C/T]AAAGTAAGGGTCCAG | 9051 |
| rs760234757 | snp | A/C/G | 0.000201379 | 0.0100326 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037071 | GCTGGACCTGTCCGC[A/C/G]GGAGACATCCTGGAG | 9051 |
| rs760300353 | snp | A/C/G | 6.80034e-05 | 0.00583075 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032378 | CCAGGCCAAGAGCAC[A/C/G]GGCACAGAGCCCCCC | 9051 |
| rs760320253 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026350 | TGCCCTGCACAGGGT[A/G]GCAGGGCAGCACACA | 9051 |
| rs760375102 | snp | G/T | 0.000116306 | 0.00762493 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018213 | TCTGGATGGCAGGAA[G/T]ATGTGCAAAGACATG | 9051 |
| rs760399670 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035278 | TGGCCTGCAGAGGGC[A/G]CCAGTGGAGGGCGTA | 9051 |
| rs760447293 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025021 | GGAGCACAGATGGTG[A/G]GGGCCTTCGGTACCT | 9051 |
| rs760512666 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000174 | AACAGGTGACAGCAC[C/T]GCTGCCGAGTGGGGC | 9051 |
| rs760526421 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011313 | CCCCTGGGAGTCCCT[C/G]GAAGCTCACAGGGCT | 9051 |
| rs760537996 | snp | A/C | 1.74467e-05 | 0.00295348 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030566 | GTGGGAGCAGGAGCA[A/C]CGGACCACCTGTGAG | 9051 |
| rs760587319 | snp | A/G | 5.39515e-05 | 0.00519354 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030514 | CAGAGCGGGTATACA[A/G]GCAGAGCATTGCGCA | 9051 |
| rs760615179 | in-del | -/CTTGCGCATGCT | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017468 | TGAATGTAGGGTGTG[-/CTTGCGCATGCT]CTGACCTGGACTGAA | 9051 |
| rs760692190 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002398 | TCTCTCCATCCCCCA[A/T]CTAATTTTCTGCAAG | 9051 |
| rs760731803 | snp | C/G | 1.7154e-05 | 0.0029286 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037222 | CTGCCAGTGGAGCCA[C/G]CAGTGCCCCCAGCAC | 9051 |
| rs760732868 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034500 | CACAGGCCCCTGAGT[A/C]ATGGCTCAGCCCCTC | 9051 |
| rs760741524 | snp | A/G | 0.000185615 | 0.00963187 | upstream-variant-2KB, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76994779 | TTGGGTCCCAGAGCA[A/G]CCAGGGTTTGATGAA | 9051 |
| rs760796603 | snp | C/G | 2.31302e-05 | 0.00340067 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025620 | GTGAGGCAGGTGCAG[C/G]GGGCGGGGGAGCTGC | 9051 |
| rs760819203 | snp | C/T | 0.00098668 | 0.0221893 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995450 | GAGTGTTGCAGACGG[C/T]GCCGGCCGGGAAGGG | 9051 |
| rs760932713 | snp | A/G | 0.0004996 | 0.0157972 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032973 | GCCCCGACAGACGGA[A/G]GGAGGGCCTAAGGCT | 9051 |
| rs760959441 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030488 | GCCCTCCCTGAGGCT[A/G]CCTGCGCTTTCAGAG | 9051 |
| rs761045877 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029689 | TGCACAATCATGGGC[A/G]CGGCGCTCTCATTCC | 9051 |
| rs761051229 | snp | C/T | 1.9969e-05 | 0.00315977 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032273 | GTGGGCATCGGGCTG[C/T]GGCCTCTGCTCTTTC | 9051 |
| rs761070276 | snp | A/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037626 | TCTTGGGGGCGGAGG[A/G]TTGAGCAGGTCCATG | 9051 |
| rs761134192 | snp | A/G | 1.66535e-05 | 0.00288556 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025344 | TACCCTGGGGCAATG[A/G]GATCTTTTGGGACTG | 9051 |
| rs761144027 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014188 | TGGGCAGATTGGGTA[A/G]CCTCTCTGGGTTACC | 9051 |
| rs761148953 | snp | C/G | 0.000165796 | 0.00910333 | intron-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77008060 | GAACAGCTGAGGATG[C/G]TTCAGGCAAGCAGAG | 9051 |
| rs761188054 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016037 | CTCTGGGGGCCTCCA[C/T]AAGGACAGGAGAAGG | 9051 |
| rs761228902 | snp | A/G | 0.000173777 | 0.00931978 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018291 | CGCAGGCAGGAAGCA[A/G]GTGGCTTCCGCTCGG | 9051 |
| rs761261239 | snp | G/T | 1.66785e-05 | 0.00288773 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031284 | GGATGATGAGGTGGG[G/T]GCTGAGGGCCTTGGT | 9051 |
| rs761464423 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999094 | AGGGTCCTCCCCCTG[C/T]CCCCAGTTTGTCGTG | 9051 |
| rs761507749 | snp | C/T | 1.69686e-05 | 0.00291273 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032368 | ACAGTTTCATCCAGG[C/T]CAAGAGCACGGGCAC | 9051 |
| rs761509510 | in-del | -/CAT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026913 | CTGTTTTGGACAGAG[-/CAT]TCTTTCTCCAAGTGG | 9051 |
| rs761534314 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026255 | CTGGAGGGCAGGCAG[G/T]ACGCAGACTGGCCTG | 9051 |
| rs761567822 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035118 | TAGAGCAGGGGCCTG[C/G]AGGGTGAGGACTGGG | 9051 |
| rs761580488 | snp | G/T | 7.7679e-05 | 0.00623165 | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032892 | AGAACTATTACGATC[G/T]GGAGGTCACCCCGCT | 9051 |
| rs761587791 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002681 | TTGCTTTGCTTTTGC[A/G]ATGCCTGCAGATGGT | 9051 |
| rs761683156 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020382 | GAGAGGTGTTCTGGG[A/C]AGTCACAAGGACAAG | 9051 |
| rs761696190 | snp | A/G | 0.00129534 | 0.0254163 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015939 | TGGGGACTTGAGCAC[A/G]GCGGTCACAGCCTGC | 9051 |
| rs761824097 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996059 | GATAAAATAGAAATC[-/A]ACACACCAACTAAAG | 9051 |
| rs761871799 | snp | C/G | 4.9943e-05 | 0.0049969 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025336 | AAGTCCCCTACCCTG[C/G]GGCAATGGGATCTTT | 9051 |
| rs761878479 | in-del | -/C | 1.99842e-05 | 0.00316097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032272 | GTGGGCATCGGGCTG[-/C]CGGCCTCTGCTCTTT | 9051 |
| rs761921103 | snp | C/G/T | 3.33351e-05 | 0.00408248 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031256 | GCAACCAGCTCTCCA[C/G/T]GCAGTGTGTCAAGGA | 9051 |
| rs761940541 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002850 | TGGCTGCTCCTGACA[C/T]CTACACAGAACTAGG | 9051 |
| rs761954911 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014103 | AGAGAGGCAAAGTAA[G/T]GGGAAGTTAACAGCC | 9051 |
| rs762071294 | in-del | -/TAAGA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003802 | AGGGTCGTCATCACT[-/TAAGA]TAAGGGCTTTGAGGT | 9051 |
| rs762096221 | snp | A/G | 5.82835e-05 | 0.005398 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037212 | CGGACCTGCCCTGCC[A/G]GTGGAGCCAGCAGTG | 9051 |
| rs762105855 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021454 | CCCATCACTTTGGGA[G/T]GCTGACCTGAGGTCA | 9051 |
| rs762112934 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001600 | CTGCCTTTGCTGCCA[A/C]CAAGTACCTTCCCGG | 9051 |
| rs762127897 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023479 | AGCTAGCGTAGGACA[A/G]TCACGAGATTTAGGA | 9051 |
| rs762234532 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995687 | ATGCAGGTGATGGGA[A/T]GCGGCTCCGAGAGGG | 9051 |
| rs762260709 | snp | A/G | 1.67273e-05 | 0.00289195 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031193 | AGGCCTTTCAGCTGC[A/G]AGAGTTTGACCGGCT | 9051 |
| rs762264110 | snp | A/T | 1.65817e-05 | 0.00287933 | missense, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995605 | AGTTCAAAGATGCCT[A/T]TTGGGTGAGTGAGGA | 9051 |
| rs762287349 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022813 | AGGGGACCTGGGGCA[G/T]GAAGGCCTGCAGCCC | 9051 |
| rs762291063 | snp | A/G | 1.67643e-05 | 0.00289515 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028629 | CGCATTAGCGCCAAC[A/G]GCCACCAGAAGCAGG | 9051 |
| rs762321048 | snp | A/G/T | 8.42288e-05 | 0.00648908 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995546 | CCTGTGGCAGGAGAG[A/G/T]GAGCTTTGCCGCGGC | 9051 |
| rs762386952 | snp | A/G | 1.78672e-05 | 0.00298886 | splice-acceptor-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035800 | TCTCACCCTGCTCTT[A/G]GCGTCCACAGAGACC | 9051 |
| rs762489652 | snp | A/G | 1.69905e-05 | 0.00291461 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029583 | GAGGCAGGTATGTGG[A/G]CCTGGCTGCCCCGTC | 9051 |
| rs762524795 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997172 | GTGGAGCTTCCTGAG[C/T]GGCATCCTGCCCACA | 9051 |
| rs762526521 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016559 | ACACGCTGCTTGTTG[C/T]TCTGTGGACAGCTGA | 9051 |
| rs762544206 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024011 | TCCGCCTCTTACCGC[A/G]GGGTGGCCACGGGCG | 9051 |
| rs762659028 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998022 | GTGGATGGATCACTT[C/G]AGGTCAGGAGTTCAA | 9051 |
| rs762667938 | snp | A/C/T | 0.000205772 | 0.0101415 | stop-gained, synonymous-codon, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035926 | GGCGCTCTACGATTA[A/C/T]ACAGCGCAGGTGAGG | 9051 |
| rs762675447 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009022 | CATGGGTGGTCCTGG[A/G]GAGCCCCTCAACTCT | 9051 |
| rs762695285 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019042 | GTGATGGGAAAGTAA[C/T]GCAGCCCTCCTCAAA | 9051 |
| rs762710246 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005728 | GCATCTCCTGTAAGT[A/G]GAATCAGATAATATT | 9051 |
| rs762726715 | snp | C/T | 1.78118e-05 | 0.00298422 | stop-gained, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037135 | GTGGAGAGGAACGGG[C/T]AGCGTGGCTTCGTCC | 9051 |
| rs762765927 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033470 | ATTCAGAATCTAAGG[A/T]CTCTCCTGGTTCAGG | 9051 |
| rs762806600 | snp | A/G | | | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007981 | TTGCCCATTGACCTG[A/G]ACCAGCTCTGAGCCC | 9051 |
| rs762824136 | snp | A/G/T | 0.000102633 | 0.0071628 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028665 | AAGGTGCGCTGGGCT[A/G/T]CTGGGCCGTGTGGGT | 9051 |
| rs762950148 | snp | C/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036352 | CTTGAGGGCCAGGCT[C/G]TGTGCCTTTGGGTCA | 9051 |
| rs762963981 | snp | G/T | 5.7351e-05 | 0.00535464 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037203 | GAGCCCCTTCGGACC[G/T]GCCCTGCCAGTGGAG | 9051 |
| rs762984900 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002633 | TGGCCGGCTGCTCAG[C/G]TGTTAGAAGATTGCA | 9051 |
| rs763044457 | snp | A/G | 1.66671e-05 | 0.00288674 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031240 | GCCCTGTGGGTGCAC[A/G]GCAACCAGCTCTCCA | 9051 |
| rs763085932 | snp | C/G | 1.80745e-05 | 0.00300615 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035780 | CAGAAGGGGAGGGGT[C/G]TATGTCTCACCCTGC | 9051 |
| rs763113631 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021922 | TCAGGTAAGGTGCTG[G/T]GGGTGCTGCATGCCC | 9051 |
| rs763190554 | snp | C/G/T | 0.000119069 | 0.00771494 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018564 | CTGGGGCTCACTCCT[C/G/T]TCCTCTGCTGGCAGT | 9051 |
| rs763249966 | snp | C/T | 1.67607e-05 | 0.00289483 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031185 | CTGCCCCCAGGCCTT[C/T]CAGCTGCAAGAGTTT | 9051 |
| rs763304812 | snp | C/T | 6.78024e-05 | 0.00582208 | utr-variant-5-prime, stop-gained, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995538 | CAGGCCAGCCTGTGG[C/T]AGGAGAGTGAGCTTT | 9051 |
| rs763308102 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021651 | ACCACTGCACTCCAG[C/T]CTGGGCTGCAGAGCG | 9051 |
| rs763319829 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011692 | GCTTATACATGGATC[A/G]CAGCAGTACTTGAGT | 9051 |
| rs763395091 | snp | A/C | 9.46074e-05 | 0.00687712 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028545 | AGTCACGCCCCTCCA[A/C]ACCCCCAGTCCAAGA | 9051 |
| rs763396089 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031547 | AGAGCCACAGAGCAC[C/G]TGCCCCCTCTGCCGG | 9051 |
| rs763450694 | snp | A/C | 0.00010295 | 0.00717385 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027828 | GGCCGCGGCCCTCGG[A/C]TCAGAACCTCGTGTC | 9051 |
| rs763450847 | snp | C/T | 1.92213e-05 | 0.00310005 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032423 | TGCGGACAGCGCAGC[C/T]TCTAGGTGCATTGAG | 9051 |
| rs763487771 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023737 | CCCTGAGCTCTGGGA[A/G]GGGTCTGGGTATGCT | 9051 |
| rs763514785 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006515 | TCATATCAGAGAAAT[A/C]ATTGCCAAATTAAAT | 9051 |
| rs763533981 | snp | A/G | 0.000168648 | 0.00918127 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008108 | GAGATCAGCACAGAA[A/G]TCTGGATCAGTGTCC | 9051 |
| rs763588659 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003329 | CCACACCAGGACTCT[C/T]CTCTGGGTTGGCTCT | 9051 |
| rs763610165 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024026 | AGGGTGGCCACGGGC[G/T]CAGCTCCTTCACTCC | 9051 |
| rs763622460 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033864 | GTGCAAGCAGTGACC[C/T]CAGGAGGCAGCACAC | 9051 |
| rs763691940 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998103 | ATTAGCCAGGCGTGA[C/T]GGCATGCTCCTGTAA | 9051 |
| rs763750790 | in-del | -/GTGT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011257 | CCACACTCATGCACA[-/GTGT]GTCCTTGTCCAGTGC | 9051 |
| rs763860522 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009043 | CCTCAACTCTCTGAG[C/T]CTTGGTTCCTTGTTT | 9051 |
| rs763875932 | snp | C/G | 3.33712e-05 | 0.00408466 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031293 | GGTGGGGGCTGAGGG[C/G]CTTGGTGTGGGGTAA | 9051 |
| rs763933015 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997191 | ATCCTGCCCACACTC[C/T]GTGCTCGTCGCACCT | 9051 |
| rs763966994 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018314 | CCGCTCGGCTCCTGG[A/G]ACAGTGGACGAGGCC | 9051 |
| rs763986763 | snp | C/T | 8.78928e-05 | 0.00662862 | intron-variant, synonymous-codon, stop-gained, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032887 | CTACCAGAACTATTA[C/T]GATCGGGAGGTCACC | 9051 |
| rs764014004 | snp | A/T | 3.31477e-05 | 0.00407096 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995639 | TTGGGGGCACTGAAC[A/T]AGTGGAGGGGGCAGA | 9051 |
| rs764043431 | snp | A/C/T | 0.000116326 | 0.00762559 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032831 | TGGGGTGTTGGGGGC[A/C/T]GCCCTGGGGCTCACG | 9051 |
| rs764046395 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028413 | TCCGGACCCCCAGAT[A/C]CCTGTCCCTGGTGAG | 9051 |
| rs764052990 | in-del | -/G | 0.000294855 | 0.0121384 | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995422 | GCTCCTCTCTGGCTC[-/G]TGGCTGCCTTCTGAG | 9051 |
| rs764124737 | snp | A/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017383 | GGCAAGCAGGGCAAG[A/T]GCCAGGCAGCAGAGG | 9051 |
| rs764170867 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036769 | GATGAGCACCCGTGA[C/T]CCCTGACATGCTCCA | 9051 |
| rs764284079 | snp | A/G | 1.68015e-05 | 0.00289836 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037087 | GGAGACATCCTGGAG[A/G]TGATCCTGGAAGGGG | 9051 |
| rs764354810 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002605 | CGTTCATCTGTGCCC[A/T]TTCCACAGGACGTGG | 9051 |
| rs764357664 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011817 | TGGGCGCTCCTCACC[A/T]GTCAAAGCCCCCCAC | 9051 |
| rs764392248 | snp | C/T | 6.25039e-05 | 0.00559 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995481 | GGGCCTGGGCCAGCC[C/T]TGCCAGGACTGGGAC | 9051 |
| rs764497481 | snp | A/C | 0.000184179 | 0.00959456 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028547 | TCACGCCCCTCCACA[A/C]CCCCAGTCCAAGAAG | 9051 |
| rs764570494 | snp | A/G | 1.79419e-05 | 0.0029951 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035794 | TCTATGTCTCACCCT[A/G]CTCTTAGCGTCCACA | 9051 |
| rs764573662 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018956 | CTGGGTTCCGGTGTC[A/G]GCTCCTCACCCCCCA | 9051 |
| rs764585617 | in-del | -/G/GG/GGG | 0.00190612 | 0.0308263 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035604 | AAACACACTGATCCT[-/G/GG/GGG]GGGGGGGAGGAGAGG | 9051 |
| rs764623622 | snp | A/G | 0.000119546 | 0.00773037 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035572 | TCTGCTGGTAAAGGG[A/G]GTCAGGAGGGGACCC | 9051 |
| rs764658426 | snp | A/G | 0.000418918 | 0.0144666 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028655 | GCAGGTGGAGAAGGT[A/G]CGCTGGGCTGCTGGG | 9051 |
| rs764705613 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994275 | TAGTCCAGGGCTCTT[C/T]CTAAGGTGGTACCAC | 9051 |
| rs764732336 | snp | A/G | 0.00253816 | 0.0355336 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995542 | CCAGCCTGTGGCAGG[A/G]GAGTGAGCTTTGCCG | 9051 |
| rs764759485 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032648 | CTCCCACGGCCCCCA[C/T]TCCCCGCCTGTTTGG | 9051 |
| rs764970796 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011543 | AGGTGAACAAAGAGT[C/T]GCTCATCTGACATTA | 9051 |
| rs765024735 | snp | C/T | 1.77751e-05 | 0.00298115 | synonymous-codon, nc-transcript-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035806 | CCTGCTCTTAGCGTC[C/T]ACAGAGACCCTGACC | 9051 |
| rs765030211 | snp | C/T | 5.03766e-05 | 0.00501854 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037081 | TCCGCGGGAGACATC[C/T]TGGAGGTGATCCTGG | 9051 |
| rs765069251 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006711 | AGTCTGTCCTTTTCT[A/C]ATAGAATGGTCTTGG | 9051 |
| rs765072290 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002793 | TCTGCTTCTTGATGA[-/C]CCACTTTGTGCTCCA | 9051 |
| rs765113383 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027231 | CCTCATAACCCAGTC[A/G]CTGTCCTGGCTGTTT | 9051 |
| rs765142004 | snp | A/G | 3.94027e-05 | 0.00443844 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032529 | AGAAGCCCTAGCAGG[A/G]GTTGTGGGGAGTTGG | 9051 |
| rs765158033 | snp | A/G | 3.88553e-05 | 0.00440751 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028569 | TCCAAGAAGACATAC[A/G]AGCAGAAGTGCCGGG | 9051 |
| rs765187272 | snp | C/T | 0.000155131 | 0.00880576 | missense, nc-transcript-variant, synonymous-codon | PSTPIP1 | GRCh38.p7 | 15:77035546 | GTCCCAAGACCACTT[C/T]GTTGGCAGCTTCTGC | 9051 |
| rs765213101 | snp | C/G | 2.29271e-05 | 0.00338571 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032442 | AGGTGCATTGAGCCC[C/G]TGGGAAGGCCCGGCC | 9051 |
| rs765298349 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017120 | AGCACCTCTCAAGCT[C/T]CCCTGGAGTAAGCCT | 9051 |
| rs765316799 | snp | C/G | 1.77322e-05 | 0.00297755 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030521 | GGTATACAGGCAGAG[C/G]ATTGCGCAGCTGGAG | 9051 |
| rs765346318 | snp | A/G/T | 4.93766e-05 | 0.00496849 | synonymous-codon, nc-transcript-variant, missense, stop-gained | PSTPIP1 | GRCh38.p7 | 15:77035529 | TGGACTGCTGCACGG[A/G/T]AGTCCCAAGACCACT | 9051 |
| rs765410751 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011408 | ATCTCTGGGACTCGG[C/T]CAGCTGGGCTGCTCA | 9051 |
| rs765423624 | snp | A/G | 1.78153e-05 | 0.00298452 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030584 | GACCACCTGTGAGGT[A/G]AGTGGCCCACGTGGA | 9051 |
| rs765505392 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021619 | GGGAGACGGAGGTTG[C/G]AGTGAGCCCAGATTG | 9051 |
| rs765550656 | snp | C/T | 1.68496e-05 | 0.0029025 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018451 | CAAATGCCCTTTTTT[C/T]TGCAGGGCCCAGGCG | 9051 |
| rs765685334 | snp | C/T | 2.41327e-05 | 0.00347358 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995363 | ATTTTGCTGCTGATT[C/T]TAGCCCCAAACAAAA | 9051 |
| rs765738253 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029727 | TGCCGTCAAAGTAAA[C/T]GCTGTGTTCCCCCAT | 9051 |
| rs765740878 | snp | A/G | 1.70194e-05 | 0.00291709 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027872 | GGCCGTCATGGACCG[A/G]GTCCAGAAGAGCAAG | 9051 |
| rs765764833 | snp | G/T | 1.7042e-05 | 0.00291903 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032988 | GGGAGGGCCTAAGGC[G/T]GGGCCAGGAAGTGGG | 9051 |
| rs765781946 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004375 | TGCCAGCTGGAGCCC[C/T]GGAGACCAGCAGCCA | 9051 |
| rs765795513 | snp | C/G | 0.000109164 | 0.00738717 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027819 | GCCTCCCGAGGCCGC[C/G]GCCCTCGGCTCAGAA | 9051 |
| rs765840750 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994419 | GGGGGTCTATTAAGG[C/T]CCCTCAGCCCCTGAA | 9051 |
| rs765845344 | snp | G/T | 1.75188e-05 | 0.00295958 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032400 | GAGCCCCCCGGTGAG[G/T]TCCGGCTTGCGGACA | 9051 |
| rs765845480 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021829 | CCCTGCCCAGTCCCA[C/T]CCATCCCTCAAGGCC | 9051 |
| rs765860049 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995696 | ATGGGATGCGGCTCC[A/G]AGAGGGGAGCTTTCT | 9051 |
| rs766018345 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006681 | ATATCCAGTTTTCCC[A/G]GCGCCATTTGTTGAA | 9051 |
| rs766141606 | snp | A/G | 0.000122429 | 0.00782301 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018234 | CAAAGACATGGAGGA[A/G]CTACTGAGGCAGAGG | 9051 |
| rs766145397 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008073 | TGGTTCAGGCAAGCA[A/G]AGCTGGGGGTGGAGG | 9051 |
| rs766186988 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017096 | TGGTGACAAAAATCC[C/T]GTCTCCCCAGCACCT | 9051 |
| rs766188597 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005709 | ATGGATTTGCCTATT[C/G]TAGGCATCTCCTGTA | 9051 |
| rs766211878 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026351 | GCCCTGCACAGGGTG[G/T]CAGGGCAGCACACAG | 9051 |
| rs766269900 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999364 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGGTCAG | 9051 |
| rs766271155 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035290 | GGCGCCAGTGGAGGG[C/T]GTAGCTGGGGAAGGA | 9051 |
| rs766351379 | snp | A/C/G | 0.000101253 | 0.00711458 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037018 | GCAGGCCCTTCCAAC[A/C/G]TCATGCGCTTTCAAT | 9051 |
| rs766458487 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997574 | AATTGAGGCACGGAG[-/AT]ATATTAAGAGACTTG | 9051 |
| rs766483694 | snp | C/T | 1.71584e-05 | 0.00292898 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037226 | CAGTGGAGCCAGCAG[C/T]GCCCCCAGCACTGTC | 9051 |
| rs766489616 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009152 | GATAAGGAGCCCCAC[A/G]TGCCATCCCCTGCAG | 9051 |
| rs766561019 | snp | C/T | 5.57833e-05 | 0.00528096 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032980 | CAGACGGAGGGAGGG[C/T]CTAAGGCTGGGCCAG | 9051 |
| rs766576017 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020578 | CTACTATGTGCCATG[A/C]CCTGGATGGGTCAGG | 9051 |
| rs766660164 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019408 | CCCCTTCCCTTCCTG[C/T]CTTCTCCCCCGAGAG | 9051 |
| rs766707210 | snp | A/G | 1.79615e-05 | 0.00299674 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030515 | AGAGCGGGTATACAG[A/G]CAGAGCATTGCGCAG | 9051 |
| rs766715642 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004097 | TCCTGTGAGGTCAGT[A/G]TTCTTATTCCTGTTT | 9051 |
| rs766821339 | snp | G/T | 1.66579e-05 | 0.00288595 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025355 | AATGGGATCTTTTGG[G/T]ACTGCGAGGCTGGTG | 9051 |
| rs766895096 | snp | C/T | 1.71664e-05 | 0.00292966 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032320 | AGGAAGTGCGGCTGA[C/T]GCTGGAAGGCTGCAG | 9051 |
| rs767004933 | snp | C/T | 1.68932e-05 | 0.00290625 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037014 | CCCTGCAGGCCCTTC[C/T]AACGTCATGCGCTTT | 9051 |
| rs767028878 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998137 | CAGCTACTTGGGAGG[C/T]TGAGGCAGGAGAACA | 9051 |
| rs767037629 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005411 | ACAAAACAAAAATTA[A/C]CATTGCTGACAATAG | 9051 |
| rs767080141 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006323 | TTGGTTGTCTTTTTA[C/T]TGTTGAGTTGAAGGA | 9051 |
| rs767229111 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015378 | CCTCCTGTCCCCATC[C/T]TCGCCTCCCGAGATC | 9051 |
| rs767229155 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026258 | GAGGGCAGGCAGGAC[A/G]CAGACTGGCCTGGAG | 9051 |
| rs767244980 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999187 | GGCTGACAAGTGGGG[C/T]ACTGGCTGAGGACGT | 9051 |
| rs767248102 | snp | A/G | 1.69755e-05 | 0.00291332 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032371 | GTTTCATCCAGGCCA[A/G]GAGCACGGGCACAGA | 9051 |
| rs767253537 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018294 | AGGCAGGAAGCAGGT[A/G]GCTTCCGCTCGGCTC | 9051 |
| rs767272289 | snp | C/G | 0.000393275 | 0.0140172 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027836 | CCCTCGGCTCAGAAC[C/G]TCGTGTCCCCTGCAG | 9051 |
| rs767276899 | snp | A/G | 8.50232e-05 | 0.00651954 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029596 | GGGCCTGGCTGCCCC[A/G]TCCGACCAGGGCGGA | 9051 |
| rs767320107 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033755 | CATTCCAGGGCCTCA[C/G]GAGCCCCTGGAACTT | 9051 |
| rs767330325 | snp | C/T | 5.76951e-05 | 0.00537068 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018193 | GAGGTGCTGCTGCAG[C/T]GGCTTCTGGATGGCA | 9051 |
| rs767335020 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998341 | CGGAGGAGGGGAGCC[A/G]GCCCTGCTGTTTCTG | 9051 |
| rs767395396 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034430 | GGCCTTGGCCCTCGG[C/T]GCCTCATGTGGGAAA | 9051 |
| rs767515719 | snp | C/T | 0.000162061 | 0.00900025 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015941 | GGGACTTGAGCACGG[C/T]GGTCACAGCCTGCAG | 9051 |
| rs767576422 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008612 | ATGGGGTTTCATCAT[C/G]TTGACCAGGCTTGTC | 9051 |
| rs767659452 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022251 | CTGACGCTGGCTCAT[C/T]GTGGGCACAGCCTCA | 9051 |
| rs767751096 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024660 | CACTGGGTGTCCTGT[G/T]TTTATGTGTTCATTC | 9051 |
| rs767763933 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001705 | GACCTGGTGTTCCCT[C/G]TAAAAAGCAGAGAGC | 9051 |
| rs767824630 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002908 | CTTGCTTTGGGCTTT[G/T]AAGGGTGGGTGAGGA | 9051 |
| rs767826067 | in-del | -/T | 0.00789624 | 0.0623359 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018444 | ATCTTTCAAATGCCC[-/T]TTTTTTTTGCAGGGC | 9051 |
| rs767839065 | snp | G/T | 3.81425e-05 | 0.0043669 | intron-variant, synonymous-codon, stop-gained, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032893 | GAACTATTACGATCG[G/T]GAGGTCACCCCGCTG | 9051 |
| rs767855367 | in-del | -/G | 0.000196367 | 0.00990682 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032972 | GCCCCGACAGACGGA[-/G]GGGAGGGCCTAAGGC | 9051 |
| rs767891976 | snp | C/T | 5.29787e-05 | 0.00514651 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032566 | GGCCTGCTGCCTCCT[C/T]TCAGGCAAAGCTAAG | 9051 |
| rs767910971 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014125 | TTAACAGCCAAGATC[G/T]TGGCTTGGGATATCT | 9051 |
| rs767988851 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999833 | CCCCGCAACCTGTAT[C/G]TCTATCCAATGGCCT | 9051 |
| rs767993227 | snp | C/T | 1.67405e-05 | 0.00289309 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035488 | CGGGGACACTCACCC[C/T]CTTTCCTCCCTGTTC | 9051 |
| rs768010225 | snp | C/T | 0.0001831 | 0.00956642 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025240 | TGGACTGTAGGTTCC[C/T]GCTGTGCTCTCCTCC | 9051 |
| rs768053271 | snp | A/G | 1.65792e-05 | 0.00287912 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995612 | AGATGCCTTTTGGGT[A/G]AGTGAGGATGGTTGG | 9051 |
| rs768152191 | snp | A/C/T | 1.99994e-05 | 0.00316217 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030493 | CCCTGAGGCTGCCTG[A/C/T]GCTTTCAGAGCGGGT | 9051 |
| rs768226088 | snp | A/G | 1.73327e-05 | 0.00294381 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030546 | CTGGAGAAGGTCCGG[A/G]CTGAGTGGGAGCAGG | 9051 |
| rs768276150 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026213 | CTTGTCAGGGAGGCT[G/T]CAGGGCTGAAGTTGG | 9051 |
| rs768294337 | in-del | -/A | 1.68866e-05 | 0.00290569 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037017 | GCAGGCCCTTCCAAC[-/A]GTCATGCGCTTTCAA | 9051 |
| rs768384245 | in-del | -/GG | 5.00939e-05 | 0.00500444 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031301 | TGAGGGCCTTGGTGT[-/GG]GGGGTAAGGTAGGGC | 9051 |
| rs768395688 | snp | C/T | 8.65089e-05 | 0.00657624 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025557 | CTGCGTGAGGAGCTG[C/T]GGAGTCTCGAGGAGT | 9051 |
| rs768425112 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020232 | GGTGGAGGCTCTGGG[C/T]GGCCCTGATTGCGCC | 9051 |
| rs768632688 | snp | A/G | 0.000162318 | 0.00900736 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032957 | ATGATAAAGAGGTGA[A/G]GCCCCGACAGACGGA | 9051 |
| rs768644555 | snp | C/T | 0.000142096 | 0.0084278 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027700 | AGGGTCACTGTGAAG[C/T]AGCAGGCTCTGGGGG | 9051 |
| rs768651472 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013998 | GAAGGTGTTTCTGGT[C/T]GGGGAGGTGGCAGGC | 9051 |
| rs768664787 | snp | A/G | 7.01164e-05 | 0.00592058 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035835 | CCCCCACCCCCGAGC[A/G]GAATGAGGGTGTCTA | 9051 |
| rs768720816 | snp | A/G | | | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995514 | TGCTGCTGGCGCCTG[A/G]CCCTCCATCAGGCCA | 9051 |
| rs768779510 | snp | A/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037566 | CAGGAGGATGTGGCA[A/G]GGGCAAGAAGGGGCT | 9051 |
| rs768887430 | snp | C/T | 1.66671e-05 | 0.00288674 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031245 | GTGGGTGCACAGCAA[C/T]CAGCTCTCCATGCAG | 9051 |
| rs768897476 | snp | C/T | 1.99694e-05 | 0.0031598 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035895 | GAAACCCGGCCTCAC[C/T]AGCCCAGGAGTACCG | 9051 |
| rs768909794 | in-del | -/TCTC | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994515 | CTTGATAATCCTGTT[-/TCTC]TCTCCATCCATTCCC | 9051 |
| rs768925344 | in-del | -/CTCTAAGGC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033422 | CAAGTCATTCACACT[-/CTCTAAGGC]CAGGGCCCTGAGTGT | 9051 |
| rs768925525 | snp | C/T | 0.000198079 | 0.00994988 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007885 | AAGTGTGAGCCACCG[C/T]GCCCGACTGGCAATA | 9051 |
| rs769000458 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996558 | AGCCCTGCCCTCCCC[A/G]GGCCTTTTCCTGGGG | 9051 |
| rs769008649 | snp | A/G | 0.000111433 | 0.00746352 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032491 | GACCGGGCTGGGGTA[A/G]CTCACAGCTCCCTTC | 9051 |
| rs769059391 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022714 | CTCCTTGAAATTTCA[C/T]CTGGGGCCAAGAAAG | 9051 |
| rs769092173 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007203 | CTCACTCTTCTTCAA[A/G]GAGGGTCTGGAGGGA | 9051 |
| rs769151896 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034300 | TGCTGGCTTGCACCC[C/T]GTCCTTTGCTGCCTG | 9051 |
| rs769215417 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020000 | AACTCAGAGACTCAG[C/G]AGAGGTGGAGAGGGT | 9051 |
| rs769216847 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007361 | GCCTGTAATTCCAGC[A/G]CTCTGGAAAGCTGAG | 9051 |
| rs769222897 | snp | C/T | 0.000148313 | 0.00861014 | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032865 | TGCTGTCTGCAGCTC[C/T]GGTGCCCTACCAGAA | 9051 |
| rs769264931 | snp | C/T | 3.34739e-05 | 0.00409095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029523 | GCTTCCCCTCTGTTT[C/T]CTCAGAGTCAGAACA | 9051 |
| rs769318378 | snp | C/T | 4.92405e-05 | 0.00496163 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028622 | CTTCGAGCGCATTAG[C/T]GCCAACGGCCACCAG | 9051 |
| rs769328313 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018015 | AGGTCTGGAGTCCCA[A/G]GAGCTTGCCCTGAGC | 9051 |
| rs769369261 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997975 | GGGTGCAGTGGTTCA[C/T]GCCTGTAATCCCAGC | 9051 |
| rs769402326 | snp | A/C | 2.28972e-05 | 0.0033835 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030475 | AGCTCGTGTCAGGGC[A/C]CTCCCTGAGGCTGCC | 9051 |
| rs769455506 | snp | A/G | 7.10808e-05 | 0.00596115 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77029568 | AAGGACTCGGCCACC[A/G]AGGCAGGTATGTGGG | 9051 |
| rs769469133 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018289 | AGCGCAGGCAGGAAG[C/G]AGGTGGCTTCCGCTC | 9051 |
| rs769495757 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002565 | CATATTTTGTGGTAC[A/G]TGGGCCTCTGGGGAC | 9051 |
| rs769531623 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018949 | GACACACCTGGGTTC[C/T]GGTGTCAGCTCCTCA | 9051 |
| rs769587319 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028104 | CGCTATGGCCCCGTG[A/G]GGATGGTCCCGGGCC | 9051 |
| rs769601842 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037398 | TGCTCAGTTCAGAGG[A/C]GGCAAAGGAACAAGG | 9051 |
| rs769673883 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019099 | TGAGGCCTGGTTAGA[-/G]GGCAGGCCGTCAGGG | 9051 |
| rs769796913 | in-del | -/AG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034039 | CCCAGAGAGGATTAG[-/AG]AGAGAGAGAGAGAGA | 9051 |
| rs769856427 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032083 | CCTTAGAGGACAGGT[A/G]TGAGTTAAGTCCCTT | 9051 |
| rs769888202 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013919 | CTCTGGTGGAGGAAG[A/G]TGTGTAGGGCGAGAG | 9051 |
| rs769979854 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023237 | TCCTCAAGGGCTCAT[C/G]GTTCAGCTGCGTGAC | 9051 |
| rs769994487 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022284 | ACAGGGAGCCGAGAG[C/G]GCTACTCCTGTCAGC | 9051 |
| rs770015686 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029589 | GGTATGTGGGCCTGG[C/T]TGCCCCGTCCGACCA | 9051 |
| rs770056297 | snp | G/T | 1.66056e-05 | 0.00288141 | missense, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995579 | ACGCCTGAGGATGAT[G/T]CCCCAGCTGCAGTTC | 9051 |
| rs770101069 | snp | A/G | 1.81955e-05 | 0.0030162 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035775 | GTCCCCAGAAGGGGA[A/G]GGGTCTATGTCTCAC | 9051 |
| rs770139775 | snp | C/T | 1.67832e-05 | 0.00289677 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037062 | CCCAGATGAGCTGGA[C/T]CTGTCCGCGGGAGAC | 9051 |
| rs770168257 | snp | C/T | 1.66718e-05 | 0.00288715 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028540 | CCCCAAGTCACGCCC[C/T]TCCACACCCCCAGTC | 9051 |
| rs770171631 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005249 | AATGTAGCCAGGTAT[A/G]GTGGTGCATGCCTGT | 9051 |
| rs770215969 | snp | A/T | 1.69588e-05 | 0.00291189 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032362 | ACATCGACAGTTTCA[A/T]CCAGGCCAAGAGCAC | 9051 |
| rs770223833 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016783 | AATACCTTCTCCTTC[C/T]AGCACCTGACTCAAA | 9051 |
| rs770292686 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018846 | GCAGGTGACAGGCGT[C/T]TCCACTGGTGGCTCA | 9051 |
| rs770392024 | snp | A/G | 9.26655e-05 | 0.00680619 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032482 | AAGTGCCAGGACCGG[A/G]CTGGGGTAGCTCACA | 9051 |
| rs770400128 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021466 | GGAGGCTGACCTGAG[A/G]TCAGGAGTTCGAGAC | 9051 |
| rs770462479 | snp | A/G | 0.000121183 | 0.0077831 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028639 | CCAACGGCCACCAGA[A/G]GCAGGTGGAGAAGGT | 9051 |
| rs770508341 | snp | A/G | | | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007876 | TGGGATTACAAGTGT[A/G]AGCCACCGCGCCCGA | 9051 |
| rs770515255 | snp | A/C | 0.000249553 | 0.0111675 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032506 | GCTCACAGCTCCCTT[A/C]AGGGCAGAGAAGCCC | 9051 |
| rs770543515 | snp | A/C | 0.000527454 | 0.0162311 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032845 | CCGCCCTGGGGCTCA[A/C]GGCTTGCTGTCTGCA | 9051 |
| rs770551607 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018348 | ATCCCAGCCAAACTC[C/T]GTCAGAACACGCCCT | 9051 |
| rs770630112 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027118 | CTTGGGTGTTTTGTG[C/T]TGTGTGTGTGTGAGT | 9051 |
| rs770669179 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028054 | ACCTCGGCCTTGGGC[A/G]CACCAGCCTGCGGGG | 9051 |
| rs770678587 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036888 | TGGGAGGCCCGGTCC[A/G]TTGGGTTACCCCCAT | 9051 |
| rs770734649 | in-del | -/GGT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020879 | CCTGTGGGGGGGGGG[-/GGT]GTGTGTGTTGGCCCT | 9051 |
| rs770854984 | snp | A/G | 0.000117433 | 0.00766177 | intron-variant, splice-acceptor-variant | PSTPIP1 | GRCh38.p7 | 15:77027798 | CCGTCCTCTTGGCCT[A/G]GGGGAGCCTCCCGAG | 9051 |
| rs770866575 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997498 | TTCTCAAGATGTATG[C/T]ATATTCACTCATTCA | 9051 |
| rs770936704 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994092 | TCATCTGCAGCAGCT[C/T]TCATCTTATCACCCC | 9051 |
| rs770958110 | snp | C/T | 1.66896e-05 | 0.00288869 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031212 | GTTTGACCGGCTGAC[C/T]ATTCTCCGCAACGCC | 9051 |
| rs770983844 | snp | G/T | 1.81618e-05 | 0.0030134 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032409 | GGTGAGGTCCGGCTT[G/T]CGGACAGCGCAGCCT | 9051 |
| rs771016278 | in-del | -/CCAGAAATA | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994328 | ACCAAACTGGAAATT[-/CCAGAAATA]TTCTCGACACCGTCT | 9051 |
| rs771019913 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006233 | AATGATGTTGAGCAT[A/C]TTTTCATGTGTTTAT | 9051 |
| rs771119941 | snp | G/T | 1.91323e-05 | 0.00309286 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995509 | GACGCTGCTGCTGGC[G/T]CCTGGCCCTCCATCA | 9051 |
| rs771172891 | snp | A/G | 0.000631455 | 0.0177575 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995451 | AGTGTTGCAGACGGC[A/G]CCGGCCGGGAAGGGG | 9051 |
| rs771181172 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004962 | CCAATGCCCAGGCCA[C/T]ACCCCAGGTCAATTA | 9051 |
| rs771184167 | snp | C/G | 4.99488e-05 | 0.00499719 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77035521 | AGGTTCTCTGGACTG[C/G]TGCACGGAAGTCCCA | 9051 |
| rs771190487 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010143 | ACTTGCCCTCACTGT[C/T]GGCCTCCTTCCTCGC | 9051 |
| rs771212940 | snp | G/T | 0.000100649 | 0.00709327 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027950 | CCGCGGCCTTCCCTC[G/T]AGGAGCAGCGCAGGT | 9051 |
| rs771232034 | snp | C/T | 0.000158883 | 0.00891158 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030523 | TATACAGGCAGAGCA[C/T]TGCGCAGCTGGAGAA | 9051 |
| rs771269246 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015751 | GAAGGAGGAGGGCGC[A/G]GGCTGGGGGAAGGGG | 9051 |
| rs771327426 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025974 | TGAGTCCAAGGATCA[A/G]GGCTGATTGTCCTGG | 9051 |
| rs771394337 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025241 | GGACTGTAGGTTCCC[A/G]CTGTGCTCTCCTCCT | 9051 |
| rs771543664 | snp | C/T | 1.69856e-05 | 0.00291419 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031136 | AGCCTGGCCGGGCCC[C/T]GCAGCCGCCTCCTCA | 9051 |
| rs771546492 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026729 | TGTGGGGTTCTGAGC[A/G]GACAGGGGGTCCCCA | 9051 |
| rs771610063 | snp | C/T | 1.72829e-05 | 0.00293959 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036995 | CCCCTCCCTGCAGGC[C/T]CTTCCCTGCAGGCCC | 9051 |
| rs771629261 | snp | A/C | 6.7579e-05 | 0.00581248 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77018519 | GGAAGGCAGGTGGCC[A/C]GACGGAGATCAAGTA | 9051 |
| rs771630326 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998935 | GATGATAAAGAGCAT[C/G]ACACCTTGGCAGGAA | 9051 |
| rs771696051 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016931 | GAGTCATGTGTGTGC[A/G]ACCCTGGAGTGTGCG | 9051 |
| rs771697508 | snp | C/T | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036111 | ACTAGCAAGGGTACC[C/T]GGGAGTGTGCTTGGA | 9051 |
| rs771697755 | snp | C/G | 0.00131527 | 0.0256106 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027749 | CCCTCTCTCCAGAGC[C/G]AGGAGAGGTGCTGCG | 9051 |
| rs771731148 | in-del | -/C | 8.16493e-05 | 0.0063889 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029592 | ATGTGGGCCTGGCTG[-/C]CCCGTCCGACCAGGG | 9051 |
| rs771740478 | snp | A/G | 1.70015e-05 | 0.00291555 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037117 | GAGGATGGCTGGTGG[A/G]CTGTGGAGAGGAACG | 9051 |
| rs771760145 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035159 | CGAGGCCTCAGTGCG[A/G]AGGTCCTAGAACCCC | 9051 |
| rs771780234 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999998 | CACTGCAGTGACTGT[C/G]ACCCACCCTTTGGGT | 9051 |
| rs771795157 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021430 | GGCGCCGTGCCTCAC[A/G]CCTATAATCCCATCA | 9051 |
| rs771800739 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011207 | TTCATGACAGACAGT[A/G]GCTGCCTCGTGGTCA | 9051 |
| rs772012977 | snp | A/C | 9.05777e-05 | 0.00672909 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995498 | GCCAGGACTGGGACG[A/C]TGCTGCTGGCGCCTG | 9051 |
| rs772016173 | snp | A/C | 1.73592e-05 | 0.00294606 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030558 | CGGGCTGAGTGGGAG[A/C]AGGAGCACCGGACCA | 9051 |
| rs772059561 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014104 | GAGAGGCAAAGTAAT[A/G]GGAAGTTAACAGCCA | 9051 |
| rs772096060 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020315 | TGGCCCTGGATGGTC[C/T]TCCCTGTCTCTGAGT | 9051 |
| rs772106169 | snp | C/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993946 | GGAGGTGAGGGCCTT[C/G]TGGGGGCAGTCCCAT | 9051 |
| rs772159881 | snp | A/C | 5.03791e-05 | 0.00501867 | synonymous-codon, nc-transcript-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77035517 | TCCCAGGTTCTCTGG[A/C]CTGCTGCACGGAAGT | 9051 |
| rs772164207 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033757 | TTCCAGGGCCTCAGG[A/C]GCCCCTGGAACTTCC | 9051 |
| rs772189813 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030401 | TCCCATGGGGGAGGC[A/G]GGGCTCCCAGTGGGA | 9051 |
| rs772313911 | snp | A/G | 1.69758e-05 | 0.00291335 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032346 | TGCAGCATAGACGCC[A/G]ACATCGACAGTTTCA | 9051 |
| rs772315853 | snp | A/G | 8.94414e-05 | 0.00668676 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025576 | GTCTCGAGGAGTTTC[A/G]TGAGAGGCAGAAGGA | 9051 |
| rs772415441 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024916 | CATTTGGTACCTGCC[A/G]AGGAGAGAGGGCTGT | 9051 |
| rs772432781 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015777 | AGGGGTGCAGGGCTG[A/G]GAGGCATCGTGAGCA | 9051 |
| rs772434207 | snp | A/G | 0.000368596 | 0.0135706 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018109 | TGCTCAGTGTCGCCT[A/G]GTCGTGGCCCTCATG | 9051 |
| rs772549153 | snp | C/T | 0.000280151 | 0.011832 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77029560 | GGCAGTGCAAGGACT[C/T]GGCCACCGAGGCAGG | 9051 |
| rs772635009 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029039 | TCTCAGAGCCAGGAA[A/G]CAGCAGAAAAGGGAC | 9051 |
| rs772637686 | in-del | -/CCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031972 | GACCCACTCTCCTAG[-/CCC]CAAGGCCTGGCTGTG | 9051 |
| rs772639391 | snp | A/G | 0.000545603 | 0.0165077 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007972 | CCTGAACAATTGCCC[A/G]TTGACCTGGACCAGC | 9051 |
| rs772683394 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027054 | TGCACACGTGCCTAC[A/G]CTCCCCTGCATATGC | 9051 |
| rs772773568 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996831 | CGGAGGACCAGGCAC[C/T]AGGATGCTCAGGGCC | 9051 |
| rs772826713 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018048 | GGGAGATGGAGGCAG[C/G]AGGGAGGCTGTTCCC | 9051 |
| rs772834374 | snp | A/T | | | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031235 | GCAACGCCCTGTGGG[A/T]GCACAGCAACCAGCT | 9051 |
| rs772912791 | snp | C/T | 1.70359e-05 | 0.0029185 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037119 | GGATGGCTGGTGGAC[C/T]GTGGAGAGGAACGGG | 9051 |
| rs772925275 | snp | A/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017031 | GGGGTCCTCAGGGAT[A/T]GAAAGGAAGACAGAC | 9051 |
| rs772961805 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000136 | GCCACACTGGGAGGA[A/G]CTGAGCCTCCCCAAG | 9051 |
| rs772968186 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036649 | GGAAGCCAGGCCAGG[-/A]AGAGTGATGGGGTAC | 9051 |
| rs772975585 | snp | A/G | 2.02624e-05 | 0.00318289 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032431 | GCGCAGCCTCTAGGT[A/G]CATTGAGCCCCTGGG | 9051 |
| rs773118317 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011308 | TGGGACCCCTGGGAG[C/T]CCCTGGAAGCTCACA | 9051 |
| rs773121842 | snp | A/C | 3.39461e-05 | 0.00411969 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032347 | GCAGCATAGACGCCG[A/C]CATCGACAGTTTCAT | 9051 |
| rs773172907 | snp | A/G | 4.81452e-05 | 0.00490615 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032970 | GAGGCCCCGACAGAC[A/G]GAGGGAGGGCCTAAG | 9051 |
| rs773348199 | snp | A/G | 0.000182262 | 0.00954451 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032268 | GCAGAGTGGGCATCG[A/G]GCTGCGGCCTCTGCT | 9051 |
| rs773353170 | snp | A/G | 1.74215e-05 | 0.00295134 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030563 | TGAGTGGGAGCAGGA[A/G]CACCGGACCACCTGT | 9051 |
| rs773398515 | snp | A/G | 0.000165769 | 0.00910258 | intron-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77008057 | CCAGAACAGCTGAGG[A/G]TGGTTCAGGCAAGCA | 9051 |
| rs773425108 | snp | A/G | 1.77187e-05 | 0.00297641 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035854 | TGAGGGTGTCTACAC[A/G]GCCATCGCAGTGCAG | 9051 |
| rs773446029 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004000 | GTTCACCATTGCATG[G/T]TATACTCCACCATTA | 9051 |
| rs773447995 | in-del | -/TCT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034832 | TCTGCCGCATCTGCC[-/TCT]TCTGTTTTATTTTCC | 9051 |
| rs773463039 | snp | C/G | 0.000185753 | 0.00963545 | upstream-variant-2KB, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76994758 | TCCTTGAGGGCAGGA[C/G]CTGGTTTGGGTCCCA | 9051 |
| rs773465943 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997832 | CTACTCTGGCCACAG[G/T]TGTTATATTAGGAAC | 9051 |
| rs773600159 | snp | A/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037625 | TTCTTGGGGGCGGAG[A/G]GTTGAGCAGGTCCAT | 9051 |
| rs773634876 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025081 | TTGCTTTAATTTGCA[A/G]AGAGCTTTGTCTTCC | 9051 |
| rs773636914 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014156 | GGGTTATATCCCAGC[A/T]GCACCCGGCAGGTCC | 9051 |
| rs773642122 | snp | A/G | 1.65787e-05 | 0.00287907 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995614 | ATGCCTTTTGGGTGA[A/G]TGAGGATGGTTGGGG | 9051 |
| rs773651879 | snp | A/G | 3.33356e-05 | 0.00408248 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031257 | CAACCAGCTCTCCAT[A/G]CAGTGTGTCAAGGAT | 9051 |
| rs773727005 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023568 | GTTTCTGGTGTGTAT[A/C]GCTGGTGGACAGTGG | 9051 |
| rs773771259 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033324 | ATCTGGAGAATTCTC[C/T]AGGCTTTTCCAGGGC | 9051 |
| rs773783878 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997502 | CAAGATGTATGCATA[C/T]TCACTCATTCAATCC | 9051 |
| rs773814876 | snp | A/C | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997855 | TTAGGAACAGCCCAG[A/C]CAGCTTGGCCCATGT | 9051 |
| rs773832598 | snp | C/T | 2.2904e-05 | 0.003384 | missense, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035913 | CCCAGGAGTACCGGG[C/T]GCTCTACGATTATAC | 9051 |
| rs773839829 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999090 | AGGAAGGGTCCTCCC[C/T]CTGCCCCCAGTTTGT | 9051 |
| rs773868993 | in-del | -/GA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036806 | GCGTCTCCAGAATGG[-/GA]GAGGGGAGGTGAGGC | 9051 |
| rs773930299 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999895 | AGGGAAAATCTAGTT[A/C]TGGACCAGATTCTAT | 9051 |
| rs773979058 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010336 | TGGAGGGGATCATGC[A/G]TGAGAGCCCCACCAG | 9051 |
| rs773989632 | snp | C/G | 1.69994e-05 | 0.00291538 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037008 | GCCCTTCCCTGCAGG[C/G]CCTTCCAACGTCATG | 9051 |
| rs774006820 | in-del | -/GGA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013120 | CACTGCTGGTGTGAG[-/GGA]GGAGAGCACCCCAGC | 9051 |
| rs774034892 | snp | C/G | 8.32882e-05 | 0.00645269 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018282 | CATGGGGAGCGCAGG[C/G]AGGAAGCAGGTGGCT | 9051 |
| rs774043213 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026227 | TGCAGGGCTGAAGTT[C/G]GATATAGGTTCCCTG | 9051 |
| rs774125430 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035084 | ACCCCTACCCATGGG[A/G]GAAGCTGCTAGGGCA | 9051 |
| rs774164456 | snp | A/G | 0.000127137 | 0.00797199 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032888 | TACCAGAACTATTAC[A/G]ATCGGGAGGTCACCC | 9051 |
| rs774180413 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034407 | TGCGCATGTGTGTGC[A/C]CTCCTGGGGCCTTGG | 9051 |
| rs774185594 | snp | A/G | | | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77029544 | AGTCAGAACAAAGCC[A/G]GGCAGTGCAAGGACT | 9051 |
| rs774196031 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009049 | CTCTCTGAGCCTTGG[G/T]TCCTTGTTTGTAAAT | 9051 |
| rs774200277 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020266 | GTTATTCAAGGCCAG[A/G]TGGGGCAGGGTCTGC | 9051 |
| rs774209733 | snp | A/G | 8.79546e-05 | 0.00663096 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025567 | AGCTGCGGAGTCTCG[A/G]GGAGTTTCGTGAGAG | 9051 |
| rs774212289 | snp | C/T | 0.000129146 | 0.0080347 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032962 | AAAGAGGTGAGGCCC[C/T]GACAGACGGAGGGAG | 9051 |
| rs774250534 | in-del | -/GTGT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020880 | CTGTGGGGGGGGGGG[-/GTGT]GTGTGTTGGCCCTCA | 9051 |
| rs774320125 | snp | A/C | 5.85394e-05 | 0.00540983 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037211 | TCGGACCTGCCCTGC[A/C]AGTGGAGCCAGCAGT | 9051 |
| rs774394333 | snp | C/T | 1.66668e-05 | 0.00288672 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031249 | GTGCACAGCAACCAG[C/T]TCTCCATGCAGTGTG | 9051 |
| rs774437204 | snp | A/G | 1.7505e-05 | 0.00295841 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035840 | ACCCCCGAGCGGAAT[A/G]AGGGTGTCTACACAG | 9051 |
| rs774457119 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013376 | CATGGGGTACCCACA[C/T]TGCACTGCCAGCTGC | 9051 |
| rs774530073 | snp | C/T | 0.000206505 | 0.0101592 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028624 | TCGAGCGCATTAGCG[C/T]CAACGGCCACCAGAA | 9051 |
| rs774537400 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028490 | TGGGCTAAGGGAGCC[C/T]CACTCCCGGGGACCA | 9051 |
| rs774539506 | in-del | -/G | 0.000111241 | 0.00745708 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032837 | GTTGGGGGCCGCCCT[-/G]GGGCTCACGGCTTGC | 9051 |
| rs774568065 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014008 | CTGGTCGGGGAGGTG[A/G]CAGGCAGGCGGGGAG | 9051 |
| rs774585049 | snp | C/T | 0.000134544 | 0.00820085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032496 | GGCTGGGGTAGCTCA[C/T]AGCTCCCTTCAGGGC | 9051 |
| rs774595063 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996816 | CTGCCTCAGCCCATC[C/T]GGAGGACCAGGCACC | 9051 |
| rs774782175 | snp | C/T | 1.78934e-05 | 0.00299105 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035797 | ATGTCTCACCCTGCT[C/T]TTAGCGTCCACAGAG | 9051 |
| rs774825441 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032363 | CATCGACAGTTTCAT[C/T]CAGGCCAAGAGCACG | 9051 |
| rs774879827 | snp | C/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993187 | GCAGAATGATGTACC[C/T]GGTGCTGGGTAAGTA | 9051 |
| rs774891463 | snp | C/T | 0.000245399 | 0.0110743 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032870 | TCTGCAGCTCCGGTG[C/T]CCTACCAGAACTATT | 9051 |
| rs774920106 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997992 | CCTGTAATCCCAGCA[C/G]TCTGGGAGGCCAAGG | 9051 |
| rs774955960 | snp | A/T | 7.53949e-05 | 0.00613936 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029580 | ACCGAGGCAGGTATG[A/T]GGGCCTGGCTGCCCC | 9051 |
| rs774963534 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007410 | CCCAGGAGTTCAAGA[C/T]TAGCCTAGGAAGCAT | 9051 |
| rs774979589 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033464 | GGTCAGATTCAGAAT[C/T]TAAGGACTCTCCTGG | 9051 |
| rs774986109 | snp | C/T | 0.000388954 | 0.0139401 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007896 | ACCGCGCCCGACTGG[C/T]AATAGAACACTTTGA | 9051 |
| rs774988146 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001570 | AGGAGGTGGGAGAGA[G/T]AGGCCCTGGCCATCC | 9051 |
| rs775039223 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999840 | ACCTGTATGTCTATC[C/T]AATGGCCTTTGCAAA | 9051 |
| rs775041579 | snp | C/T | 3.31631e-05 | 0.00407191 | missense, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995602 | TGCAGTTCAAAGATG[C/T]CTTTTGGGTGAGTGA | 9051 |
| rs775087018 | in-del | -/CT | 9.00597e-05 | 0.00670982 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030480 | GTGTCAGGGCCCTCC[-/CT]GAGGCTGCCTGCGCT | 9051 |
| rs775128176 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034341 | ACGTGTGTCTGCCCG[C/T]CTGTGTTGGTGTCAG | 9051 |
| rs775142183 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018991 | TCTGACCATGGGCTG[G/T]CTGCTGACACACTCT | 9051 |
| rs775147429 | snp | A/C | 0.000116802 | 0.00764116 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018561 | GCCCTGGGGCTCACT[A/C]CTCTCCTCTGCTGGC | 9051 |
| rs775189141 | snp | A/G | 6.60131e-05 | 0.00574476 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030482 | GTCAGGGCCCTCCCT[A/G]AGGCTGCCTGCGCTT | 9051 |
| rs775226824 | snp | C/T | 1.73766e-05 | 0.00294755 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037202 | GGAGCCCCTTCGGAC[C/T]TGCCCTGCCAGTGGA | 9051 |
| rs775253052 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997696 | TGGATCTTTTGGCTT[C/T]GGGGTAAGATAAGAG | 9051 |
| rs775279893 | snp | A/G | 0.000166931 | 0.00913442 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008084 | AGCAGAGCTGGGGGT[A/G]GAGGGCGGGAGATCA | 9051 |
| rs775344858 | snp | A/G | 2.0114e-05 | 0.00317122 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032535 | CCTAGCAGGGGTTGT[A/G]GGGAGTTGGGTCCCA | 9051 |
| rs775345543 | snp | A/G | 1.77059e-05 | 0.00297533 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037134 | TGTGGAGAGGAACGG[A/G]CAGCGTGGCTTCGTC | 9051 |
| rs775395200 | snp | A/C | 1.6601e-05 | 0.00288101 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995582 | CCTGAGGATGATGCC[A/C]CAGCTGCAGTTCAAA | 9051 |
| rs775494272 | snp | A/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036342 | CAGGTCATAGCTTGA[A/G]GGCCAGGCTCTGTGC | 9051 |
| rs775514550 | snp | G/T | 3.62325e-05 | 0.00425617 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035776 | TCCCCAGAAGGGGAG[G/T]GGTCTATGTCTCACC | 9051 |
| rs775550898 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014155 | TGGGTTATATCCCAG[C/T]TGCACCCGGCAGGTC | 9051 |
| rs775598661 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001852 | TTAAAGTGGTTGCCT[A/G]TTGGGAGAATGAGAG | 9051 |
| rs775601632 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021640 | GCCCAGATTGCACCA[C/T]TGCACTCCAGCCTGG | 9051 |
| rs775632005 | snp | A/G | 1.67863e-05 | 0.00289704 | splice-acceptor-variant | PSTPIP1 | GRCh38.p7 | 15:77031178 | CCTCCCACTGCCCCC[A/G]GGCCTTTCAGCTGCA | 9051 |
| rs775649978 | snp | G/T | 3.44857e-05 | 0.00415231 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995526 | CTGGCCCTCCATCAG[G/T]CCAGCCTGTGGCAGG | 9051 |
| rs775685983 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001344 | ATCCCCCATAGTCCT[C/T]TGGTTGGGCAGGAGC | 9051 |
| rs775764738 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031361 | ATCTGAGCCGGTCAA[C/T]AAGCACCTGGTCCTC | 9051 |
| rs775772984 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006460 | CATTTTGATGAATTC[A/G]ATGTGTCTACTCTTT | 9051 |
| rs775791697 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016831 | AGCTCTCCTGGATTT[C/T]GACTCCATCCCTGTT | 9051 |
| rs775796638 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995267 | GGTCCCAGACTGTGT[C/T]CTCCATCACCGCAGG | 9051 |
| rs775811275 | snp | A/G | 1.7277e-05 | 0.00293908 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032314 | TCTACGAGGAAGTGC[A/G]GCTGACGCTGGAAGG | 9051 |
| rs775866529 | in-del | C/TCCATCCATCCATCCATCCAT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012136 | CCATCCATCCATCCA[C/TCCATCCATCCATCCATCCAT]CCACCCACCCACCCA | 9051 |
| rs775888406 | snp | A/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994153 | GGTGATTTGCGGACA[A/G]TCCCTGACTCACCCC | 9051 |
| rs776027050 | snp | C/G | 1.69663e-05 | 0.00291253 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032366 | CGACAGTTTCATCCA[C/G]GCCAAGAGCACGGGC | 9051 |
| rs776085567 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016029 | TCTTTCCACTCTGGG[G/T]GCCTCCATAAGGACA | 9051 |
| rs776205276 | snp | C/T | 0.000296311 | 0.0121683 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028541 | CCCAAGTCACGCCCC[C/T]CCACACCCCCAGTCC | 9051 |
| rs776250362 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996982 | AGGGCAGGCCAGGAC[C/T]CCTTGACTATTTTAT | 9051 |
| rs776256698 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008945 | CCTTTACTTGGCAGG[C/T]GCCATCTTTGTCTCT | 9051 |
| rs776293497 | snp | C/T | 1.6643e-05 | 0.00288465 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025278 | CTGGACCCATCTGTT[C/T]TGCAGCTCCCTGAGG | 9051 |
| rs776337082 | snp | A/G | 0.000102359 | 0.00715327 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032846 | CGCCCTGGGGCTCAC[A/G]GCTTGCTGTCTGCAG | 9051 |
| rs776340305 | snp | C/T | 0.00318471 | 0.039777 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007883 | ACAAGTGTGAGCCAC[C/T]GCGCCCGACTGGCAA | 9051 |
| rs776344540 | snp | G/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993827 | TCTATGGCCTACAAA[G/T]TTCAAGGGGATTTTT | 9051 |
| rs776473297 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036931 | AGGGGCTGCCCCTGC[C/T]CACCCTGGGAGACAT | 9051 |
| rs776482457 | snp | A/G | 1.6786e-05 | 0.00289702 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037074 | GGACCTGTCCGCGGG[A/G]GACATCCTGGAGGTG | 9051 |
| rs776520305 | snp | A/C | 0.000182476 | 0.00955012 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028506 | CACTCCCGGGGACCA[A/C]AGAACAGGGCTGTGC | 9051 |
| rs776521124 | snp | C/T | 8.19303e-05 | 0.00639988 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018435 | GTCACTGATGATCTT[C/T]CAAATGCCCTTTTTT | 9051 |
| rs776525737 | snp | A/C | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036266 | TACCTATGCCGTCCA[A/C]ACAGGCTGGGCGCTG | 9051 |
| rs776531155 | in-del | -/GCCAGGAGCCCCTTCGGACCT | 2.89147e-05 | 0.00380217 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037182 | AAGCTTTGAGGAAGG[-/GCCAGGAGCCCCTTCGGACCT]GCCAGGAGCCCCTTC | 9051 |
| rs776563737 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013078 | TGCTAGCAAACCCAC[A/T]GTGTCAGCCACACTG | 9051 |
| rs776567812 | in-del | -/GGGC | 3.31521e-05 | 0.00407123 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995627 | AGTGAGGATGGTTGG[-/GGGC]GGGCACTGAACAAGT | 9051 |
| rs776576205 | snp | A/C/G | 0.000104907 | 0.00724179 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030568 | GGGAGCAGGAGCACC[A/C/G]GACCACCTGTGAGGT | 9051 |
| rs776622175 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007561 | TTGCAGTGAGCTGTA[A/G]TCATGCCACTGCACT | 9051 |
| rs776642556 | snp | C/T | 0.000161394 | 0.00898171 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995453 | TGTTGCAGACGGCGC[C/T]GGCCGGGAAGGGGGG | 9051 |
| rs776772924 | snp | C/T | 4.0919e-05 | 0.00452304 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027810 | CCTAGGGGAGCCTCC[C/T]GAGGCCGCGGCCCTC | 9051 |
| rs776871338 | snp | A/C | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994129 | TGTAAGGCAGACATC[A/C]GTGAGGGTGGTGATT | 9051 |
| rs776877938 | snp | C/T | 1.76319e-05 | 0.00296911 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995519 | CTGGCGCCTGGCCCT[C/T]CATCAGGCCAGCCTG | 9051 |
| rs776911839 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022596 | AGAGAATGACTTTAT[-/G]GTGGCCCCCAGATCC | 9051 |
| rs776921685 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021550 | TGGGCATGGTGACGC[A/G]AGCCTGCAGTCCCAG | 9051 |
| rs776923558 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015889 | CCCAAAGCTCTGAGC[A/G]GGGGACTGGGCGGGA | 9051 |
| rs776943674 | snp | A/G | | | intron-variant, splice-acceptor-variant | PSTPIP1 | GRCh38.p7 | 15:77026115 | TCTCACCCATATGTA[A/G]GGCATGGCTGTCCCG | 9051 |
| rs776957732 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004981 | CCAGGTCAATTACAC[C/T]CCGATTTCTGAGGGT | 9051 |
| rs776988502 | snp | C/T | 3.3389e-05 | 0.00408575 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018159 | ACAGTGCAGGGACTT[C/T]ACAGCCCACACGGGC | 9051 |
| rs777014246 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021423 | GGGCCAGGCGCCGTG[-/C]CCTCACGCCTATAAT | 9051 |
| rs777062015 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015230 | TGTTCCAAAATAGAA[A/G]ATGGTTCCTGGGCTG | 9051 |
| rs777117901 | snp | C/T | 1.69166e-05 | 0.00290827 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036999 | TCCCTGCAGGCCCTT[C/T]CCTGCAGGCCCTTCC | 9051 |
| rs777128054 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028870 | CTTTGCCACCGTCAG[A/G]CGGCACTCAGGGACC | 9051 |
| rs777278328 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002160 | AACGCATTGTCAGTG[G/T]CTTCCTGACTCTGTG | 9051 |
| rs777380464 | snp | A/G | 3.34063e-05 | 0.00408681 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031205 | TGCAAGAGTTTGACC[A/G]GCTGACCATTCTCCG | 9051 |
| rs777400289 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012872 | GCCGTCATAAGGCCT[C/T]GTCCTCTTGAAGGCC | 9051 |
| rs777409558 | snp | C/G/T | | | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027892 | AGAAGAGCAAGCTGT[C/G/T]GCTCTACAAGAAGGC | 9051 |
| rs777433076 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996100 | GCAAGGGGATCCAAG[A/G]CACTAAAGCCCCCAG | 9051 |
| rs777438227 | snp | A/G | 6.14137e-05 | 0.00554104 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032462 | AAGGCCCGGCCCTGA[A/G]CCTCAAGTGCCAGGA | 9051 |
| rs777443039 | snp | G/T | 1.76789e-05 | 0.00297307 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035812 | CTTAGCGTCCACAGA[G/T]ACCCTGACCCCCACC | 9051 |
| rs777465250 | snp | A/G | 5.00046e-05 | 0.00499998 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025361 | ATCTTTTGGGACTGC[A/G]AGGCTGGTGGAGGGT | 9051 |
| rs777502941 | snp | C/T | 2.14516e-05 | 0.00327496 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995501 | AGGACTGGGACGCTG[C/T]TGCTGGCGCCTGGCC | 9051 |
| rs777522061 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006854 | TACTGTAGCTTTGTA[A/G]TAAGCTTTGAAATCA | 9051 |
| rs777648542 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013785 | GGTAGGAACTCGGAC[C/T]AAAACCCAGGTGTCC | 9051 |
| rs777730101 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004939 | TAGGACTGTCATTCT[A/G]AAAAATCCCAATGCC | 9051 |
| rs777790427 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031981 | TCCTAGCCCCAAGGC[C/G]TGGCTGTGCTGCATT | 9051 |
| rs777876040 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006167 | ATAGCCACCTTAGGA[G/T]GCATGAAGTAATATC | 9051 |
| rs777878418 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031085 | CAGCAGAGAGGGCTG[C/G]CCTGGTCAGCTCCGG | 9051 |
| rs777882130 | snp | C/T | 1.68103e-05 | 0.00289911 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037034 | TCATGCGCTTTCAAT[C/T]TCTTGGCCAGAACCC | 9051 |
| rs777886488 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016547 | CTTCCAGGCTAGACA[C/T]GCTGCTTGTTGCTCT | 9051 |
| rs777904557 | in-del | -/ATA | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994048 | AAACCCTGGGCATGC[-/ATA]ATAATGGGCACTTGG | 9051 |
| rs777927575 | snp | C/T | 0.0455778 | 0.143915 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035762 | TCCAGGGGCCAGTGT[C/T]CCCAGAAGGGGAGGG | 9051 |
| rs777934681 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015730 | GGAAGTGGCAGGGGT[G/T]GGGGTGAAGGAGGAG | 9051 |
| rs778120164 | snp | C/T | 3.53301e-05 | 0.00420283 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032403 | CCCCCCGGTGAGGTC[C/T]GGCTTGCGGACAGCG | 9051 |
| rs778236551 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034790 | TTGAGCCCTCACTAC[C/T]GCCCACTTCAGGGGG | 9051 |
| rs778238424 | snp | A/G | 1.73294e-05 | 0.00294353 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035605 | AAACACACTGATCCT[A/G]GGGGGGAGGAGAGGT | 9051 |
| rs778294308 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998867 | AGGAGTGAGGCAGGG[C/T]GGACCAGCCACAGAG | 9051 |
| rs778369356 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015558 | GGAGTGGGGGACAAC[C/T]AGGGTAGGTCCCCTG | 9051 |
| rs778382070 | snp | A/G | 0.000183016 | 0.00956423 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018113 | CAGTGTCGCCTGGTC[A/G]TGGCCCTCATGTGTC | 9051 |
| rs778384243 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009453 | CCTATAAGGGCTTAG[A/G]AGTCCACGTATTCTC | 9051 |
| rs778411593 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012640 | GGGGTACTGACTGTA[A/G]GGCGGTGGAAGGAGC | 9051 |
| rs778437281 | in-del | -/AG | 0.00018534 | 0.00962473 | intron-variant, frameshift-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026135 | TGGCTGTCCCGAGAC[-/AG]AGTGACTGCATGGAA | 9051 |
| rs778519998 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020854 | TGGACCTGTTTCCTC[A/G]TCTTAGACTCCTGTG | 9051 |
| rs778522775 | in-del | -/CT | 8.10668e-05 | 0.00636607 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029515 | TTAGCGCTGCTTCCC[-/CT]CTGTTTCCTCAGAGT | 9051 |
| rs778618707 | snp | C/T | 5.01433e-05 | 0.00500691 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031199 | TTCAGCTGCAAGAGT[C/T]TGACCGGCTGACCAT | 9051 |
| rs778633833 | snp | C/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036068 | TCCTCTCCTCCTCAG[C/G]AGGGCACGTGTGCCC | 9051 |
| rs778642250 | snp | A/G/T | 5.1675e-05 | 0.00508284 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032394 | GGCACAGAGCCCCCC[A/G/T]GTGAGGTCCGGCTTG | 9051 |
| rs778658906 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021320 | AACATCCGTGGGGCA[A/G]TGGCAATGGAGGATG | 9051 |
| rs778695339 | snp | C/T | 1.69801e-05 | 0.00291372 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032344 | GCTGCAGCATAGACG[C/T]CGACATCGACAGTTT | 9051 |
| rs778842895 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999101 | TCCCCCTGCCCCCAG[C/T]TTGTCGTGGCTCCAC | 9051 |
| rs778856736 | snp | A/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993835 | CTACAAAGTTCAAGG[A/G]GATTTTTACACTATT | 9051 |
| rs778862175 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004801 | GGAGTTGGAAACTGT[A/G]GTGACTGTATGATCG | 9051 |
| rs778875283 | snp | A/T | 8.99078e-05 | 0.00670417 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027909 | CTCTACAAGAAGGCC[A/T]TGGAGGTGAGCGCCA | 9051 |
| rs778918807 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014915 | GCCACACACCATGGA[C/T]GGCGAGGGCTGGGTC | 9051 |
| rs778979854 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031910 | GCCCAAGTGACTCGA[-/G]CCCCCTGCTGCCTCC | 9051 |
| rs779002668 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000382 | CCCTACCCCCAGACC[-/A]TGTCTACCATGGCCC | 9051 |
| rs779042881 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024839 | CCTCCAAACATCCCC[C/T]GGGCCACCTGCTGAG | 9051 |
| rs779120528 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034023 | GGGCAGAAAGGAGTG[C/G]CCCCAGAGAGGATTA | 9051 |
| rs779243313 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013877 | AGGGAGCATTTGAAA[A/G]AGGCTCTGCTCCCCT | 9051 |
| rs779251444 | snp | C/T | 3.64864e-05 | 0.00427105 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035959 | TCTATACCCCAAACC[C/T]ACCTGTGCCACCTCC | 9051 |
| rs779260117 | snp | C/T | 0.000122854 | 0.00783657 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037184 | AGCTTTGAGGAAGGG[C/T]CAGGAGCCCCTTCGG | 9051 |
| rs779290323 | snp | A/G | 7.00906e-05 | 0.00591949 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032832 | GGGGTGTTGGGGGCC[A/G]CCCTGGGGCTCACGG | 9051 |
| rs779324739 | snp | A/G | 3.51494e-05 | 0.00419207 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018270 | TGCTGGGCAGGCCAT[A/G]GGGAGCGCAGGCAGG | 9051 |
| rs779332305 | snp | A/C | 3.22118e-05 | 0.00401309 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032924 | ACCAGCAGCCCTGGC[A/C]TACAGCCGTCCTGCG | 9051 |
| rs779352987 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004108 | CAGTATTCTTATTCC[C/T]GTTTTACAGAGAGGA | 9051 |
| rs779397550 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011022 | TGGCCCCATGAGAGT[A/G]AAGGAGGGGAAGCAG | 9051 |
| rs779415805 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009423 | ACAGCCGCAAAGCAG[C/G]CACCTCATATCAGCC | 9051 |
| rs779434097 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008843 | ACTCTAAGTAGAGTC[A/G]TGTTTCTCCACCATG | 9051 |
| rs779552936 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001002 | CGTAACTCACTCCAT[C/T]GGGAACACCTGTGGG | 9051 |
| rs779595119 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021090 | AACAGGGTGCAGAAC[A/G]AGGACAAAAGCCAGG | 9051 |
| rs779613545 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030871 | TCTGGGTGCTGCCGA[G/T]GGACAGGGCCTGGGG | 9051 |
| rs779639304 | snp | C/G | 5.75093e-05 | 0.00536203 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035476 | CTGAGTGTGGGGCGG[C/G]GACACTCACCCTCTT | 9051 |
| rs779697620 | in-del | -/CCT | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035970 | AACCCACCTGTGCCA[-/CCT]CCCCTGCACCTGAGA | 9051 |
| rs780004889 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003768 | TTCTGAACCTCAGTT[C/T]CCTCATCTGCAGGAT | 9051 |
| rs780029805 | snp | A/C | 0.000184792 | 0.0096105 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026183 | GGGAGGTGTGTAAGC[A/C]GAGGCTGGCAGATGC | 9051 |
| rs780062879 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023281 | GCCAGCCCAAAGTGA[C/T]ATCAGTGCTCAGAAA | 9051 |
| rs780080026 | snp | A/G | 1.70226e-05 | 0.00291736 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032334 | ACGCTGGAAGGCTGC[A/G]GCATAGACGCCGACA | 9051 |
| rs780092404 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033155 | CAAGGGACCCAGACA[C/T]TAGAATAATCACACC | 9051 |
| rs780094550 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008720 | CAGCATTCTTGATCT[C/G]AGTCCTACCTCTGTG | 9051 |
| rs780097396 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014872 | AGAGCCTCCTCCTGG[A/G]GTTCTGGGATGCCGC | 9051 |
| rs780114159 | in-del | -/ATT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011077 | CTTTCCTGCCTCATC[-/ATT]GAGAAGGCCTATTTA | 9051 |
| rs780115979 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997595 | AAGAGACTTGCGCAA[C/G]GTCACACTGCTGGGA | 9051 |
| rs780139580 | snp | A/G | 0.00016193 | 0.0089966 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016005 | GCCAGCGTAGGTTCG[A/G]TTTGCTTCTCTTTCC | 9051 |
| rs780159547 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024589 | AAAGTCCGTTTTAAA[C/T]ACTACAAGGGGCATA | 9051 |
| rs780203700 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996487 | CCCGGGGTGCTGCCT[C/T]CAACCCCGAAGAGGA | 9051 |
| rs780242570 | snp | C/T | 8.50376e-05 | 0.00652009 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029504 | GGGGCAGGGGCTTAG[C/T]GCTGCTTCCCCTCTG | 9051 |
| rs780297337 | snp | A/G | 4.47758e-05 | 0.00473137 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028613 | GGAGCAGGCCTTCGA[A/G]CGCATTAGCGCCAAC | 9051 |
| rs780439410 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007165 | ATCTATGACATCTCG[G/T]CTTCCTTGAGGCCCC | 9051 |
| rs780442836 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017224 | GAATGTCCTGGGAGA[C/T]CTCTGTTCCTTCATA | 9051 |
| rs780532289 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032678 | GTTCCACTGGATCAC[A/G]GGTCCAGAATATTAG | 9051 |
| rs780551403 | snp | A/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993357 | CAGTTGCTCCAGCCC[A/G]TCACCAGCATGGCCC | 9051 |
| rs780589319 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001782 | AAGCATTTATACTGG[C/T]GCAGGCTTGTAGTAT | 9051 |
| rs780602931 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007099 | AGAGGGCCCCTGGGT[C/T]GTGGGCTCCTCCCTG | 9051 |
| rs780629410 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029965 | CTTCACTTGATGCCC[A/G]AATCCTACCAACACT | 9051 |
| rs780685211 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017823 | GGCCTGGCTGTCATC[-/A]GGGGGACTTAAGGGT | 9051 |
| rs780766539 | snp | G/T | 1.67019e-05 | 0.00288975 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031305 | GGGCCTTGGTGTGGG[G/T]TAAGGTAGGGCAGCC | 9051 |
| rs780773859 | snp | C/G/T | 9.335e-05 | 0.00683139 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032483 | AGTGCCAGGACCGGG[C/G/T]TGGGGTAGCTCACAG | 9051 |
| rs780782245 | snp | C/T | 0.000125683 | 0.00792628 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007815 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9051 |
| rs780817214 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002353 | TTCCCTACATGTTAA[C/T]ACTGGTGTCTATGGA | 9051 |
| rs780817999 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018891 | CTGGCTCAGCATGGG[C/T]TTCAAGGATGGAGAT | 9051 |
| rs780825166 | snp | A/C | 7.04473e-05 | 0.00593454 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035820 | CCACAGAGACCCTGA[A/C]CCCCACCCCCGAGCG | 9051 |
| rs780836028 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029098 | CTCCTGATGCTGTGG[A/C]CCCTAGGCCAGAGTG | 9051 |
| rs780907089 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013834 | TTAGCTGTCCTCTGA[C/T]AGATGCTGTATTCTG | 9051 |
| rs781039621 | snp | A/G | 0.000185305 | 0.00962384 | intron-variant, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026130 | GGGCATGGCTGTCCC[A/G]AGACAGAGTGACTGC | 9051 |
| rs781045469 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028697 | GCCCAGGGCTGGGGG[A/C]AGTGGGGGAGGCAAG | 9051 |
| rs781069265 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998738 | TCAGCATGGGAGCAG[-/AC]ACAGTCCTGTCCCTC | 9051 |
| rs781102926 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014619 | GTGTCTGTGGTCTCG[C/T]CCCTGCAGCCACCAA | 9051 |
| rs781119554 | in-del | -/TCCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024731 | TGCTGGGCCCTTCCC[-/TCCC]TCCCTCCCTCCCTCC | 9051 |
| rs781153246 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997408 | TCTGGATTCTAATAC[C/G]TCTTCCTGATGCTCA | 9051 |
| rs781189399 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024353 | CTGCTCCTCCTTGGC[C/T]TCTGCTTCCCCAGGT | 9051 |
| rs781230646 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017707 | ACTTTCCAGCTGGGC[C/T]GCTCTGGATACGATC | 9051 |
| rs781251437 | snp | C/G | 1.92106e-05 | 0.00309919 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035884 | GGAGATACAGGGAAA[C/G]CCGGCCTCACCAGCC | 9051 |
| rs781258335 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007027 | ACTGGCCACGAGTCC[A/G]TGACAAACTCCTCAT | 9051 |
| rs781341816 | snp | C/T | 5.0043e-05 | 0.0050019 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031219 | CGGCTGACCATTCTC[C/T]GCAACGCCCTGTGGG | 9051 |
| rs781348955 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006252 | TCATGTGTTTATTGG[C/T]CATTTGTGTACCTTC | 9051 |
| rs781377793 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030986 | GGACCCCCTGGGCAT[C/T]TCCACCTCCCTCCCT | 9051 |
| rs781386591 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027574 | ACGACTGTGTGCGCA[C/T]GTGTGTTGGGGTGGG | 9051 |
| rs781423711 | snp | C/T | 0.000381794 | 0.0138113 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032410 | GTGAGGTCCGGCTTG[C/T]GGACAGCGCAGCCTC | 9051 |
| rs781437901 | snp | A/G | 1.68658e-05 | 0.0029039 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037102 | GTGATCCTGGAAGGG[A/G]AGGATGGCTGGTGGA | 9051 |
| rs781458430 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032060 | TCCAATGGGAAAAGT[C/G]GGGTCTACCTTAGAG | 9051 |
| rs781458957 | snp | A/G | 1.66098e-05 | 0.00288177 | missense, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995574 | GGCAGACGCCTGAGG[A/G]TGATGCCCCAGCTGC | 9051 |
| rs781498825 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999763 | TGGGTCAGGCAAGGA[A/G]TGCTCTGAGAGGAGC | 9051 |
| rs781516273 | snp | G/T | 3.83914e-05 | 0.00438112 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028596 | CGGGACGCGGACGAC[G/T]CGGAGCAGGCCTTCG | 9051 |
| rs781549267 | snp | C/T | 3.47132e-05 | 0.00416598 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030543 | CAGCTGGAGAAGGTC[C/T]GGGCTGAGTGGGAGC | 9051 |
| rs781626138 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000781 | TCTTGGGCTCAAGCA[A/G]TCCTCCTGCCTTGGC | 9051 |
| rs781630548 | snp | A/C | 6.43853e-05 | 0.00567349 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035585 | GGGGTCAGGAGGGGA[A/C]CCCCAAACACACTGA | 9051 |
| rs781666219 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026842 | AGGAAGGAGGGACCC[C/T]GGCCCTGCTATTTTG | 9051 |
| rs781698763 | snp | A/G/T | 6.04394e-05 | 0.00549691 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018479 | GCGGAGGAGCGGTAC[A/G/T]GGAAGGAGCTGGTGC | 9051 |
| rs781747543 | snp | A/G | | | synonymous-codon, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035905 | CTCACCAGCCCAGGA[A/G]TACCGGGCGCTCTAC | 9051 |
| rs781781950 | snp | C/G | 1.67925e-05 | 0.00289758 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037048 | TCTCTTGGCCAGAAC[C/G]CAGATGAGCTGGACC | 9051 |
| rs796077160 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032525 | GCAGAGAAGCCCTAG[A/C]AGGGGTTGTGGGGAG | 9051 |
| rs796082999 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024835 | ACCTCCTCCAAACAT[C/T]CCCCGGGCCACCTGC | 9051 |
| rs796089670 | in-del | -/GG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020869 | ATCTTAGACTCCTGT[-/GG]GGGGGGGGGGTGTGT | 9051 |
| rs796210927 | in-del | -/TC | | | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037329 | AGGAGTGCGTTCTGT[-/TC]TCCTTGGTGTGCTGG | 9051 |
| rs796274791 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015863 | CACTCGGCCACAGCC[C/T]CTGCCAGCAGCCCAA | 9051 |
| rs796282432 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011587 | CTCTAAAAACTAAAA[G/T]TCTGTCTTTGCCTTC | 9051 |
| rs796314460 | in-del | -/GGGT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020878 | TCCTGTGGGGGGGGG[-/GGGT]GTGTGTGTTGGCCCT | 9051 |
| rs796398939 | in-del | GGG/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020878 | CTCCTGTGGGGGGGG[GGG/T]GTGTGTGTGTTGGCC | 9051 |
| rs796493063 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034206 | AAAAGAGGTGTGGGG[-/G]CACGCAGCACAATGG | 9051 |
| rs796574336 | in-del | ACCTTGAATTGCAGGGCTGCCCCCCACAGGCCCCC/CCT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034493 | GCCCCCCACAGGCCC[lengthTooLong]AGTCATGGCTCAGCC | 9051 |
| rs796612296 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003994 | AATCATGTTCACCAT[C/T]GCATGTTATACTCCA | 9051 |
| rs796716295 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000474 | AGATATATATATATA[C/T]ATACACACACACACA | 9051 |
| rs796741604 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014091 | GTGGGGCTTTGCAGA[C/G]AGGCAAAGTAATGGG | 9051 |
| rs796852412 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015901 | AGCGGGGGACTGGGC[A/G]GGATCCTGGAGCCTG | 9051 |
| rs796945203 | in-del | -/TGGGGC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025400 | CAGAAGATGAGGTGT[-/TGGGGC]TGGGGCTGGGGCTGG | 9051 |
| rs797004642 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024793 | ACTCCTGCGCCCTGC[C/G]CTGCTAGCCTCTCCC | 9051 |
| rs797015678 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020869 | ATCTTAGACTCCTGT[-/G]GGGGGGGGGGGTGTG | 9051 |