SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs869884 | snp | C/T | 0.431029 | 0.17242 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999257 | GTCCATCTCCCTTCC[C/T]GAACCCATTTTTTAC | 9051 |
rs1022197 | snp | A/G | 0.472989 | 0.113031 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997700 | TCTTTTGGCTTCGGG[A/G]TAAGATAAGAGGTAA | 9051 |
rs1022198 | snp | C/T | 0.484138 | 0.0876334 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997820 | AGAAAAGGCACACTA[C/T]TCTGGCCACAGGTGT | 9051 |
rs1141038 | snp | C/G | 0 | 0 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018463 | GAGGCAGAGGGCCCA[C/G]GCGGAGGAGCGGTAC | 9051 |
rs1141039 | snp | A/G | 0 | 0 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025566 | GAGCTGCGGAGTCTC[A/G]AGGAGTTTCGTGAGA | 9051 |
rs1141040 | snp | A/T | 0.000118299 | 0.00768996 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028565 | CCAGTCCAAGAAGAC[A/T]TACGAGCAGAAGTGC | 9051 |
rs1141041 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028574 | GAAGACATACGAGCA[G/T]AAGTGCCGGGACGCG | 9051 |
rs1141042 | snp | A/G/T | 0.000161987 | 0.00899818 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028582 | ACGAGCAGAAGTGCC[A/G/T]GGACGCGGACGACGC | 9051 |
rs1141043 | snp | A/G/T | 3.79643e-05 | 0.00435669 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028587 | CAGAAGTGCCGGGAC[A/G/T]CGGACGACGCGGAGC | 9051 |
rs1141044 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028601 | CGCGGACGACGCGGA[G/T]CAGGCCTTCGAGCGC | 9051 |
rs1141045 | snp | C/G | 0 | 0 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028604 | GGACGACGCGGAGCA[C/G]GCCTTCGAGCGCATT | 9051 |
rs2254441 | snp | A/G | 0.475348 | 0.108251 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995677 | TGAAATCTCCATGCA[A/G]GTGATGGGATGCGGC | 9051 |
rs2458249 | snp | A/C | 0.18 | 0.24 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000460 | TATATATATATATAT[A/C]TCTCTTTAAATGCCC | 9051 |
rs2458253 | snp | A/C/T | 0.001245 | 0.0249246 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995448 | CTTCCCGGCCGGCGC[A/C/T]GTCTGCAACACTCAG | 9051 |
rs2458254 | snp | G/T | 0.476918 | 0.104919 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994528 | CTCAGTGAATGGGAA[G/T]GGATGGAGAGAGAAA | 9051 |
rs2469198 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020169 | ATGTTGCGTACCTCC[C/T]GCTTCCTGAGGCCCA | 9051 |
rs2469203 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003793 | CAGGATGTCAGGGTC[A/G]TCATCACTTAAGATA | 9051 |
rs2469207 | snp | A/G | 0.046775 | 0.145601 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011659 | ATAAATATGGGATGA[A/G]GATGACTTACAGCTG | 9051 |
rs2469229 | snp | A/C | 0.476052 | 0.106772 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994352 | TTCTCGACACCGTCT[A/C]CTTTCCAAAGACTGG | 9051 |
rs2469230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998891 | CACAGAGGGAGGGAA[A/G]GGATAATGTGATTTC | 9051 |
rs2469231 | snp | A/T | 0.154661 | 0.231107 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006350 | aggagttctttatat[A/T]ttctagatactcatc | 9051 |
rs2469232 | snp | G/T | 0.484701 | 0.0861117 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006593 | ggtcttacatctagg[G/T]gttcacttcatcttg | 9051 |
rs2469235 | snp | A/G | 0.148326 | 0.228391 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013151 | GCACCATGCAGCTCC[A/G]TGCAGCTACCTTCCA | 9051 |
rs2469236 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030195 | GCTGCCTTCTCTGAA[A/C]CTCAGTTTCCCCTCT | 9051 |
rs2469237 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030668 | TTAAAGGGGCCCAAG[C/T]GAGGCAGTTGGGGAA | 9051 |
rs3812911 | snp | C/G | 0.37685 | 0.215428 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018295 | GGCAGGAAGCAGGTG[C/G]CTTCCGCTCGGCTCC | 9051 |
rs3812912 | snp | A/G | 0.105214 | 0.203807 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018305 | AGGTGGCTTCCGCTC[A/G]GCTCCTGGGACAGTG | 9051 |
rs3812913 | snp | A/T | 0.0391387 | 0.134304 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018374 | GCCCTGCTTTAAAAA[A/T]CTCTTCTGTGTTCCC | 9051 |
rs3812914 | snp | C/T | 0.0149638 | 0.0851937 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77018543 | TCAAGTAAGATCTCC[C/T]GGGCCCTGGGGCTCA | 9051 |
rs3812915 | snp | C/G | 0.109461 | 0.206758 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028146 | GGGCTCGTGAATGAA[C/G]GGCAGATGAAGTCAG | 9051 |
rs3812916 | snp | A/C/T | 0.0541834 | 0.155422 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031319 | GGTAAGGTAGGGCAG[A/C/T]CTCTAGGCAGCAAAG | 9051 |
rs3841234 | in-del | -/TT | 0.0836354 | 0.186609 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028121 | GATGGTCCCGGGCCC[-/TT]CCCTTGTGGGGCTCG | 9051 |
rs3935339 | snp | A/G | 0.40386 | 0.197046 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029688 | GAATGAGAGCGCCGC[A/G]CCCATGATTGTGCAG | 9051 |
rs3936040 | snp | A/G | 0.254385 | 0.249962 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022791 | AGGTCCCCTGTCCCC[A/G]TTGCTGGAACCATCA | 9051 |
rs4075475 | snp | A/G | 0.0998734 | 0.199905 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017078 | GGCCTGCCTTGGTGC[A/G]GTTGGTGACAAAAAT | 9051 |
rs4078354 | snp | C/T | 0.439661 | 0.162877 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032539 | GGCCTGGGACCCAAC[C/T]CCCCACAACCCCTGC | 9051 |
rs4420499 | snp | G/T | 0.212728 | 0.247206 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022633 | AGATCAGAGCTCAAG[G/T]CTGTTCACTTTGGGG | 9051 |
rs4886508 | snp | C/T | 0.418974 | 0.184249 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015569 | CAACTAGGGTAGGTC[C/T]CCTGGGGGTGATGCT | 9051 |
rs5021805 | snp | A/G | 0.217851 | 0.247924 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997959 | GACTGGTTTTTAGGC[A/G]GGGTGCAGTGGTTCA | 9051 |
rs6495232 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035080 | CCCCACCCCTACCCA[C/T]GGGGGAAGCTGCTAG | 9051 |
rs7167993 | snp | A/T | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000716 | CTTTTACAAATTTTT[A/T]Atttttgcagagatg | 9051 |
rs7173067 | snp | A/G | 0.475702 | 0.107512 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016046 | CCTCCATAAGGACAG[A/G]AGAAGGGTTCCCTTG | 9051 |
rs7175783 | snp | G/T | 0.491263 | 0.0655142 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010924 | GTGCTGGGATTTCAG[G/T]TGTGAGCCACCACGT | 9051 |
rs7176360 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998519 | CCACAATTTTAATGA[G/T]CTTGGTCATGGGGTC | 9051 |
rs8029854 | snp | C/T | 0.478271 | 0.101943 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021690 | TCTTAAAAAAAAAGA[C/T]AGTGTTAGTATTTGC | 9051 |
rs8030698 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011398 | CAGCCCAGGCATCTC[C/T]GGGACTCGGCCAGCT | 9051 |
rs9707978 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035236 | CTAGGATCCTCCCAA[A/G]GGCCCTGCAGGGAGC | 9051 |
rs9806416 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035230 | GGGGTTCTAGGATCC[C/T]CCCAAGGGCCCTGCA | 9051 |
rs10152353 | snp | A/G | 0.103082 | 0.202275 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030420 | CTCCCAGTGGGAGGA[A/G]GCATCCAGGATGGGA | 9051 |
rs10400889 | snp | G/T | 0 | 0 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037627 | CTTGGGGGCGGAGGG[G/T]TGAGCAGGTCCATGG | 9051 |
rs10681693 | in-del | -/TA | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000477 | ATATATATATATATA[-/TA]CACACACACACACAC | 9051 |
rs11072639 | snp | A/C | 0.228547 | 0.249078 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015060 | GGCTGTTCATGGGTT[A/C]CCCAGAGCCGCACTC | 9051 |
rs11072640 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034269 | CTGGCCGCTTCCTCC[A/T]CCTGTCCCCAGCCCC | 9051 |
rs11373069 | in-del | -/A | 1.81299e-05 | 0.00301075 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035767 | GGCCAGTGTCCCCAG[-/A]AAGGGGAGGGGTCTA | 9051 |
rs11633011 | snp | A/C | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028658 | GGTGGAGAAGGTGCG[A/C]TGGGCTGCTGGGCCG | 9051 |
rs11633907 | snp | A/C | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013977 | CCAGCCTGGCCCCAG[A/C]TGAGGGAAGGTGTTT | 9051 |
rs11636266 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025789 | GGGCAGAGGCCTGGC[C/T]GCTGGCACTAAGGCC | 9051 |
rs11637049 | snp | A/C | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003724 | cctcacccacacttg[A/C]taggtggccttggag | 9051 |
rs11639459 | snp | C/T | 0.217851 | 0.247924 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010628 | TGCTCCTTGCCTCCT[C/T]TCTCACTTTTCTTCT | 9051 |
rs11854745 | snp | C/G | 0.154661 | 0.231107 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036244 | CAGCACACACGTGGA[C/G]CACATGTACCTATGC | 9051 |
rs11855392 | snp | G/T | 0.106278 | 0.204558 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033286 | GCAGTGGCAACGCTG[G/T]CTGGCTGGAGCAGGA | 9051 |
rs11858480 | snp | C/T | 0.0941849 | 0.195504 | intron-variant, synonymous-codon, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032938 | CATACAGCCGTCCTG[C/T]GGCATGATAAAGAGG | 9051 |
rs11858973 | snp | A/T | 0.11963 | 0.213316 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036339 | CTGCAGGTCATAGCT[A/T]GAGGGCCAGGCTCTG | 9051 |
rs12050669 | snp | A/G | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023728 | atgtgcaggccctga[A/G]ctctgggaggggtct | 9051 |
rs12148413 | snp | A/G | 0.441705 | 0.160466 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023792 | GAGGGTGGTGTGCGT[A/G]AGGGCTGGGTTGGGG | 9051 |
rs12438566 | snp | A/G | 0.430285 | 0.173197 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034405 | CCTGCGCATGTGTGT[A/G]CACTCCTGGGGCCTT | 9051 |
rs12900395 | snp | C/G | 0.44651 | 0.154543 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018004 | TGTGTAAAGCCAGGT[C/G]TGGAGTCCCAAGAGC | 9051 |
rs12903227 | snp | A/C | 0.430732 | 0.172731 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030688 | CAGTTGGGGAAGGTA[A/C]CTGTTACTCACTCGT | 9051 |
rs12905311 | snp | C/T | 0.49949 | 0.0159663 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011969 | AGTGCTCCCTCTGCT[C/T]CTGATGGCCCCACAG | 9051 |
rs12906071 | snp | A/T | 0.0129783 | 0.0795028 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025643 | GGAGCTGCTCCCCCA[A/T]TGCCAGCCTCTCAGT | 9051 |
rs12908255 | snp | C/T | 0.499575 | 0.0145705 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009016 | TACACTCATGGGTGG[C/T]CCTGGGGAGCCCCTC | 9051 |
rs12912465 | snp | C/T | 0.208169 | 0.246476 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017118 | CCAGCACCTCTCAAG[C/T]TCCCCTGGAGTAAGC | 9051 |
rs12913937 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023790 | TGGAGGGTGGTGTGC[A/G]TAAGGGCTGGGTTGG | 9051 |
rs12915411 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014166 | ccagctgcacccggc[A/C]ggtccctgggcagat | 9051 |
rs12916725 | snp | C/G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014169 | gctgcacccggcagg[C/G/T]ccctgggcagattgg | 9051 |
rs16968616 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015387 | CCCATCTTCGCCTCC[C/T]GAGATCTGTGTTGTG | 9051 |
rs16968623 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019700 | CTCCAGCGAGCTGCC[A/G]TGCAAATCAACAAGA | 9051 |
rs16968625 | snp | A/G | 0.304688 | 0.243945 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020110 | ATTTACAGCAGGGAA[A/G]GAGAAGCTACCCACA | 9051 |
rs16968627 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020485 | ATGAAGTACTGTTGA[C/T]GAGGCCATGCAGCTG | 9051 |
rs17380886 | snp | C/G | 0.43088 | 0.172575 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998939 | ATAAAGAGCATCACA[C/G]CTTGGCAGGAAGTTT | 9051 |
rs17465692 | snp | A/G | 0.41441 | 0.188333 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014919 | CACACCATGGACGGC[A/G]AGGGCTGGGTCCCAC | 9051 |
rs17465755 | snp | G/T | 0.21725 | 0.247846 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015411 | TGTTGTGGTCAGGAA[G/T]ATAACGCTATGATAC | 9051 |
rs28863174 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006053 | TTAACTTTTTGAGTA[A/C]CCGCCAAACAGTTTT | 9051 |
rs28939089 | snp | A/C/G | | | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032304 | CTGCCCCAGCTCTAC[A/C/G]AGGAAGTGCGGCTGA | 9051 |
rs34022353 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023072 | TGGGGGCTGGGAAAA[-/A]GGGCCAGCAGCTCCC | 9051 |
rs34066759 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034695 | TTCTCTCCTAGTAAA[-/A]GCTTCACTCATCTTT | 9051 |
rs34087066 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005039 | TTCCCCAGTGCCTCC[-/C]ATGTGGAACTTTAGC | 9051 |
rs34107915 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029627 | GGCCTGGGCGGTACT[C/T]CCCACACACACCTCC | 9051 |
rs34127110 | snp | A/G | 0.427119 | 0.176434 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021230 | CAGGCCTGGAGGCTC[A/G]GGCCACTGAAATTAA | 9051 |
rs34192860 | snp | A/G | 0.499598 | 0.0141716 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019664 | TCGCCTAGCCTCTCC[A/G]AGTTTGTTTCTCACC | 9051 |
rs34220530 | snp | C/T | 0.404209 | 0.196773 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003978 | TCAGAATGCCTCCTC[C/T]AATCATGTTCACCAT | 9051 |
rs34224655 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001703 | AGACCTGGTGTTCCC[-/C]TGTAAAAAGCAGAGA | 9051 |
rs34240327 | snp | C/G | 0.0155682 | 0.0868433 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032329 | GCGTCTATGCTGCAG[C/G]CTTCCAGCGTCAGCC | 9051 |
rs34316721 | in-del | -/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037569 | AGGATGTGGCAGGGG[-/G]CAAGAAGGGGCTCAG | 9051 |
rs34370173 | snp | A/G | 0.408359 | 0.193449 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999436 | GACGTGCGCCGCCAC[A/G]TCTGTCTAATTTTTG | 9051 |
rs34413462 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020989 | CCTGGCCTCCCTGAG[-/G]CCCACAGCTGCCCCC | 9051 |
rs34470467 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018879 | CCCCTGCAGCACTGG[-/G]CTCAGCATGGGCTTC | 9051 |
rs34500166 | snp | A/C | 0.431177 | 0.172264 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016583 | CAGCTGAGCCTGGAC[A/C]AGGCCCTCCTCAGGA | 9051 |
rs34504488 | in-del | -/A/GGA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027636 | GGTCTGCAGCAAGGA[-/A/GGA]CCTCACGGCACACCC | 9051 |
rs34612811 | snp | C/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034201 | TGGGGAAAAGAGGTG[C/T]GGGGCACGCAGCACA | 9051 |
rs34618738 | snp | C/T | 0.00886803 | 0.0659952 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018466 | CCCGTACCGCTCCTC[C/T]GCCTGGGCCCTGCAA | 9051 |
rs34659729 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016278 | GCATTCTGACATGAA[-/A]TGCTGGTGTCCCTCC | 9051 |
rs34678088 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028047 | TCCTCGGACCTCGGC[-/C]TTGGGCGCACCAGCC | 9051 |
rs34820830 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019554 | GTGTGAGGCCAGAAA[-/A]GTTGCACACAGCCCT | 9051 |
rs34827781 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014530 | AGGGCCCGAAAGGGG[-/G]TTAGCCTCCTGCCCC | 9051 |
rs34890345 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014657 | GGGCGTGAAAAGGGG[-/G]AAGTGGCGGTAGTTA | 9051 |
rs34908107 | snp | A/G | 0.00301491 | 0.0387087 | missense, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035928 | GGCCTCACCTGCGCT[A/G]TATAATCGTAGAGCG | 9051 |
rs34936469 | in-del | -/C/G | 1.7288e-05 | 0.00294002 | frameshift-variant, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032393 | GGCACAGAGCCCCCC[-/C/G]GGTGAGGTCCGGCTT | 9051 |
rs34955550 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002107 | CTGAGTGCCTGTTCC[-/C]ATGCCAGGCATGCTG | 9051 |
rs35018118 | snp | A/G | 0.408188 | 0.193589 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998856 | CACGCTGCTGTAGGA[A/G]TGAGGCAGGGCGGAC | 9051 |
rs35075154 | snp | C/T | 0.499575 | 0.0145705 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019722 | TCAACAAGAACATGG[C/T]CTGAGGGCCTCCCAA | 9051 |
rs35103653 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006366 | TCTAGATACTCATCC[-/C]TTTATCAGATATATG | 9051 |
rs35104087 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004152 | GGAAGGAATGTGGGC[-/C]TGGGGGATGCCACAC | 9051 |
rs35130368 | snp | A/C | 0.490782 | 0.0672626 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019646 | TGTGGGACTGTGGGC[A/C]AGTCGCCTAGCCTCT | 9051 |
rs35134156 | snp | A/G | 0.438526 | 0.164189 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023091 | CCAGCAGCTCCCAGA[A/G]CCTGCGATTCCTTAC | 9051 |
rs35210749 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016134 | GGAATGACAGGTCCC[-/C]TGAGAGTCCGGATTC | 9051 |
rs35274013 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999296 | CTTTTTTTTTTTTTT[-/T]GAGAAAGAATCTTAC | 9051 |
rs35336070 | snp | A/C | 0.440057 | 0.162414 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021519 | CCCCGTCTCTATCAA[A/C]AATATAAAAATTAGT | 9051 |
rs35346102 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016055 | GACAGGAGAAGGGTT[-/T]CCCTTGGCGTCAGGG | 9051 |
rs35369251 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020950 | GGCCCACCCTCCAGG[-/G]CCCATCCCTGAGTAG | 9051 |
rs35388063 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020936 | CATCGGGGCTGGTGG[-/G]CCCACCCTCCAGGGC | 9051 |
rs35393077 | snp | A/C | 0.491783 | 0.0635686 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034239 | CAGCAAGCCCTGCAC[A/C]CCTTTCCCCCTGCCC | 9051 |
rs35396658 | snp | A/G | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009877 | TCCCTGGCAGGCGTA[A/G]GTGGTGTGGGAGGGC | 9051 |
rs35480677 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003662 | TCAAAAAAAAAAAAA[-/A]GAAGAAGAAGGAAGC | 9051 |
rs35538044 | snp | C/T | 0.00861834 | 0.0650761 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035914 | TGTATAATCGTAGAG[C/T]GCCCGGTACTCCTGG | 9051 |
rs35565530 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997690 | TATCACTGGATCTTT[C/T]GGCTTCGGGATAAGA | 9051 |
rs35643710 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016224 | AGTGAGGGAAGCCGC[-/C]ACAAGGTGGTTCCCA | 9051 |
rs35677716 | snp | A/G | 0.00168963 | 0.0290165 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031189 | GGTCAAACTCTTGCA[A/G]CTGAAAGGCCTGGGG | 9051 |
rs35860563 | snp | A/G | 0.00152783 | 0.0275968 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77032342 | ACTGTCGATGTCGGC[A/G]TCTATGCTGCAGCCT | 9051 |
rs35863239 | snp | A/G | 0.492918 | 0.0590819 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019115 | GGCAGGCCGTCAGGG[A/G]AGTGGCTCTGATGAA | 9051 |
rs35900895 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034094 | TGGCTGCTGGAGGGG[-/G]CTGGTCAGGCCTCTG | 9051 |
rs35913965 | in-del | -/A | 0.487329 | 0.0839424 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033820 | CCGTGCTTAGAGAGG[-/A]GCACACACACACCCT | 9051 |
rs35984139 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007097 | TAGAGGGCCCCTGGG[-/G]TTGTGGGCTCCTCCC | 9051 |
rs35988555 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015864 | CTCGGCCACAGCCCC[-/C]TGCCAGCAGCCCAAA | 9051 |
rs36044191 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025423 | GGGCTGGGCTGGCCC[-/C]ACACGGGTGAGTTGT | 9051 |
rs36186258 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024678 | ATGTGTTCATTCTGG[-/G]CAGCCCCCGCCCATC | 9051 |
rs55775608 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025432 | CTGGCCCACACGGGT[A/G]AGTTGTGGGTGGCTG | 9051 |
rs55859202 | in-del | -/TCCACCCA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012156 | CCATCCATCCATCCA[-/TCCACCCA]CCCACCCACCCACCC | 9051 |
rs55909412 | in-del | -/CCTC/CCTG/CCTGCCTGCCTG/CCTGCCTGCCTT | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995172 | CTGCCTGCCTGCCTG[lengthTooLong]GCCCGGCCCGAGCTC | 9051 |
rs55986457 | in-del | -/G | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034202 | GGGGAAAAGAGGTGT[-/G]GGGGCACGCAGCACA | 9051 |
rs56036788 | snp | C/T | 0.375 | 0.216506 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000504 | ACACACACACACACA[C/T]ACACACACACACTTT | 9051 |
rs56103874 | snp | A/G | 0.347694 | 0.230122 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028829 | AGAGAACCTCAGGCC[A/G]TGGACAGGCAGGTCA | 9051 |
rs56175244 | snp | C/T | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000478 | ATATATATATATATA[C/T]ACACACACACACACA | 9051 |
rs56193954 | in-del | -/GATATATATA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000460 | GGGCATTTAAAGAGA[-/GATATATATA]TATATATACACACAC | 9051 |
rs56266471 | snp | A/G | 0.00323726 | 0.0401017 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032476 | AGCCTCAAGTGCCAG[A/G]ACCGGGCTGGGGTAG | 9051 |
rs56274115 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033736 | CCCTTCCCAAGGACC[A/C]GCTCATTCCAGGGCC | 9051 |
rs56293302 | snp | C/T | 0.212728 | 0.247206 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994605 | TCTAATCTGGAGACT[C/T]GCGGTGGTGGCGGTG | 9051 |
rs57036819 | snp | C/T | 0.106278 | 0.204558 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012494 | ATCCACCCATCCATC[C/T]ACCCACCCATCCATC | 9051 |
rs58564704 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032488 | AGGACCGGGCTGGGG[-/G]TAGCTCACAGCTCCC | 9051 |
rs59350137 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004879 | AAACAAACAAACAAA[A/C]AAAAAAAACAAAGAA | 9051 |
rs59777395 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029503 | TGGGGCAGGGGCTTA[G/T]CGCTGCTTCCCCTCT | 9051 |
rs59976517 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020881 | TGTGGGGGGGGGGGG[-/T]GTGTGTGTTGGCCCT | 9051 |
rs62007170 | snp | C/T | 0.21695 | 0.247806 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013796 | GGACCAAAACCCAGG[C/T]GTCCCCCTCCAAGGT | 9051 |
rs62007171 | snp | C/T | 0.3752 | 0.216391 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013944 | CGAGAGGGGAGGTGA[C/T]GAGGTGACTCATTTC | 9051 |
rs62007172 | snp | A/G | 0.21845 | 0.248001 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014400 | CCAGGGTCACGGGAG[A/G]TGTGAACCCACATCT | 9051 |
rs62007173 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015006 | CCCCTAATCCAGGAC[A/G]GGTTATCCTGGGTGC | 9051 |
rs62007205 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015614 | GGTGGCAGACCCACA[C/T]GACTGATTAAGTTAC | 9051 |
rs62007206 | snp | A/G | 0.089084 | 0.191327 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015718 | CCATGCCCTCGAGGA[A/G]GTGGCAGGGGTGGGG | 9051 |
rs62007207 | snp | G/T | 0.089084 | 0.191327 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016301 | GTCCCTCCGGGCAGG[G/T]GCAGGAGGCTGAGGC | 9051 |
rs62007209 | snp | A/G | 0.349013 | 0.229557 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019298 | CAGAGCCAGGCCAAG[A/G]GGCAGACAGACCACC | 9051 |
rs62007212 | snp | A/G | 0.297128 | 0.245518 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021051 | TGCAGAACGGGCAGG[A/G]GACTGGGGGATGGGA | 9051 |
rs62007213 | snp | G/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023906 | ATTGGAGGTGCCACT[G/T]CTGGTGAGGAGTCAG | 9051 |
rs62007214 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027512 | CAGAGTGTACACACA[C/T]GTGTGAGCGACTGTG | 9051 |
rs62027301 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997284 | GGCATATAGTTTCCC[C/T]AGGGAAGGCCAGAGC | 9051 |
rs62027302 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999846 | ATGTCTATCCAATGG[C/T]CTTTGCAAAGATGTC | 9051 |
rs62027304 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003451 | CTGAGGTCAGGGGTT[C/T]GAGACCAGCCTGGCC | 9051 |
rs62027305 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006149 | CTGTTTTTTTTTTAA[A/T]TCATAGCCACCTTAG | 9051 |
rs62027306 | snp | A/G | 0.21303 | 0.247251 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009137 | TAATGGCCAAGCAAG[A/G]ATAAGGAGCCCCACG | 9051 |
rs62027307 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010767 | ATTCTCCTGCCTCAC[C/T]CTCCGAGTAGCGGGG | 9051 |
rs62027308 | snp | C/T | 0.217851 | 0.247924 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011351 | GGTCCCTGTCAGCCA[C/T]GGGCCTGTGGGCCTC | 9051 |
rs62027309 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012156 | CCATCCATCCATCCA[C/T]CCACCCACCCACCCA | 9051 |
rs66807501 | in-del | -/T | 0.489201 | 0.0726845 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034201 | TGGGGAAAAGAGGTG[-/T]TGGGGGCACGCAGCA | 9051 |
rs67239232 | in-del | -/CCCT | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024752 | CCTCCCTCCCTCCCT[-/CCCT]GGCAGACAGTGCCCA | 9051 |
rs67501538 | snp | A/G | 0.380333 | 0.213338 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022001 | CAAGGCCAGCTTCCT[A/G]TAGCCCCTCTGTGGT | 9051 |
rs67775313 | in-del | -/TA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000459 | GGGCATTTAAAGAGA[-/TA]GATATATATATATAT | 9051 |
rs67778947 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033821 | CGTGCTTAGAGAGGG[-/A]CACACACACACCCTC | 9051 |
rs71143383 | in-del | -/A/AA | 0.264906 | 0.249555 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004687 | TAAAAAAAAAAAAAA[-/A/AA]GTACAAAAATTAGCT | 9051 |
rs71447137 | in-del | -/A | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003655 | ACGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 9051 |
rs71447138 | in-del | -/C | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035062 | TTGTGTGGCAGTGCA[-/C]CCCCCCACCCCTACC | 9051 |
rs71470045 | multinucleotide-polymorphism | ATG/GTA | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023790 | TGGAGGGTGGTGTGC[ATG/GTA]AGGGCTGGGTTGGGG | 9051 |
rs71931532 | in-del | -/AG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000455 | ATCCTGGGCATTTAA[-/AG]AGAGATATATATATA | 9051 |
rs72534062 | in-del | -/A | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033819 | CCCGTGCTTAGAGAG[-/A]GGCACACACACACCC | 9051 |
rs72643467 | snp | C/G | 0.031825 | 0.122064 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027976 | CAGGTCTCAGGGTGC[C/G]ATCCTGGGCTGTGGC | 9051 |
rs72742444 | snp | C/T | 0.259674 | 0.249813 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996316 | TAAAGTGGCTTGGCC[C/T]GGGCCACGTAGCCTG | 9051 |
rs72742446 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014930 | CGGCGAGGGCTGGGT[C/T]CCACATCTGGCTCAA | 9051 |
rs72742453 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028369 | TGAGAGCAGGACTAC[C/G]AGCAGCCCCCACGCC | 9051 |
rs73459015 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002795 | TGCTTCTTGATGACC[C/T]ACTTTGTGCTCCAGT | 9051 |
rs73459020 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009713 | AGTGGGTGATGCTCT[C/T]ATCCCGATCTCACAG | 9051 |
rs74024529 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001761 | CGTTGTGAAAAGTGG[A/G]GAAATAAGCATTTAT | 9051 |
rs74024533 | snp | C/T | 0.105214 | 0.203807 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019054 | TAACGCAGCCCTCCT[C/T]AAAGGAAGAAGTGGG | 9051 |
rs74024535 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019440 | GGAACTGAATGTGCC[A/G]TACTCTGAAGGTCCC | 9051 |
rs74025047 | snp | C/G | 0.102726 | 0.202016 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030889 | ACAGGGCCTGGGGAA[C/G]AGGGCTCAGGACTCC | 9051 |
rs74394507 | snp | A/G | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002458 | GAAAATATTTAAAAA[A/G]AAAACTAAGCAATTC | 9051 |
rs74423591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021373 | AACTCCAGGGATCCC[C/T]ACCAGCGCTTTCAGT | 9051 |
rs74522465 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023747 | TGGGAGGGGTCTGGG[C/T]ATGCTGTGGTCATGA | 9051 |
rs74545169 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011257 | CCACACTCATGCACA[C/G]TGTGTCCTTGTCCAG | 9051 |
rs74569844 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995740 | TTGATTCTTGGTCTT[A/G]ATTGTCATGGAGGTG | 9051 |
rs74702623 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021730 | ACCAACATTGCTGAC[A/G]TCACATGTCCAGCCC | 9051 |
rs74928120 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002347 | GGATGCTTCCCTACA[C/T]GTTAACACTGGTGTC | 9051 |
rs75070428 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013999 | AAGGTGTTTCTGGTC[A/G]GGGAGGTGGCAGGCA | 9051 |
rs75124538 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014918 | ACACACCATGGACGG[C/T]GAGGGCTGGGTCCCA | 9051 |
rs75368251 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003360 | GGAAGGTTCCTCCCT[C/T]ACAGACTCAGTCATG | 9051 |
rs75674469 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029899 | TTGAACCCAGGCCAT[C/T]GGGCTTCAGAGCCCA | 9051 |
rs75722829 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998843 | GAGTGTTCAGATGCA[C/T]GCTGCTGTAGGAGTG | 9051 |
rs75744288 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002675 | TCATGCTTGCTTTGC[G/T]TTTGCGATGCCTGCA | 9051 |
rs75758909 | snp | A/C | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029049 | AGGAAGCAGCAGAAA[A/C]GGGACCCCCAACTCA | 9051 |
rs75847992 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014419 | GAACCCACATCTAGT[C/T]AGTCAGACCCTTCCC | 9051 |
rs75895879 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997892 | CTTCCCCCACCCCAG[C/G]CCAAGGCACTGTCAT | 9051 |
rs76009365 | snp | G/T | 0.0494327 | 0.149241 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018385 | AAAAACTCTTCTGTG[G/T]TCCCTCAAACCTGGG | 9051 |
rs76012505 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028847 | GACAGGCAGGTCAGC[C/T]GGATCCCCTTTGCCA | 9051 |
rs76174831 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997659 | GTTGTTGCAGGATCC[C/T]TCTGTCTATCTGACA | 9051 |
rs76301451 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013254 | CCAATCCAGTCCAAG[C/T]TAGTATCACAATTTC | 9051 |
rs76332753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004461 | AACGGGAAACAGCCA[C/T]ACTGGGGAGGAAGTC | 9051 |
rs76510434 | snp | C/G | 0.067446 | 0.170804 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021716 | TTTGCAGGGGGCTTA[C/G]CAACATTGCTGACAT | 9051 |
rs76586777 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019514 | AGCCAGAGATCACAG[A/G]AAGGCTTAGATGTGG | 9051 |
rs76709699 | snp | A/C/G | 0.0444908 | 0.142359 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009987 | ATTCGGCAAGGAGCC[A/C/G]TGCTCTTCCTGTGAA | 9051 |
rs76771911 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017132 | GCTCCCCTGGAGTAA[A/G]CCTGCGTGCAGTGCC | 9051 |
rs76906988 | snp | C/G | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020388 | TGTTCTGGGCAGTCA[C/G]AAGGACAAGCAGAGA | 9051 |
rs76941698 | snp | A/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002452 | TAAAAAGAAAATATT[A/T]AAAAAGAAAACTAAG | 9051 |
rs77026017 | snp | C/T | 0.00191165 | 0.0308572 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025307 | GGGCCTCCTTTGACT[C/T]CTTGAAGCAGCGTAA | 9051 |
rs77105246 | snp | A/C | 0.0240643 | 0.107019 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994358 | ACACCGTCTACTTTC[A/C]AAAGACTGGGTGTGG | 9051 |
rs77317876 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006932 | GGCTCTTTGGGGGCC[C/T]GAGTAGAGCTGCTTT | 9051 |
rs77452498 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016185 | CAAGCAAGCCATTTC[C/T]TTCTCTGGCCTCAGT | 9051 |
rs77511922 | snp | G/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020870 | TCTTAGACTCCTGTG[G/T]GGGGGGGGGGTGTGT | 9051 |
rs77589398 | snp | G/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020879 | CCTGTGGGGGGGGGG[G/T]GTGTGTGTGTTGGCC | 9051 |
rs77736772 | snp | A/C | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003656 | ACGAAACTCCGTCTC[A/C]AAAAAAAAAAAAGAA | 9051 |
rs77775234 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001832 | ACGGATGCACAGGGA[A/G]CTAATTAAAGTGGTT | 9051 |
rs77826713 | snp | G/T | 0.039522 | 0.134904 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014713 | GTGGGGGTGTGGAGG[G/T]CCCTGGCCGGCTCAC | 9051 |
rs77897640 | snp | A/C | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003655 | AACGAAACTCCGTCT[A/C]AAAAAAAAAAAAAGA | 9051 |
rs77923689 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000656 | CATAAGATTGCCTTA[C/G]ATAGGTGCAAGCATA | 9051 |
rs77968440 | snp | C/T | 0.0123238 | 0.0775244 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032434 | CAGCCTCTAGGTGCA[C/T]TGAGCCCCTGGGAAG | 9051 |
rs78003696 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028843 | CATGGACAGGCAGGT[A/C]AGCTGGATCCCCTTT | 9051 |
rs78138579 | snp | C/T | 0.21875 | 0.248039 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015914 | GCGGGATCCTGGAGC[C/T]TGCAGCCTCTGGGGA | 9051 |
rs78141855 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009217 | GCCTCAGGCTCAGCT[C/T]CGAGGCCCTGAACCT | 9051 |
rs78154879 | snp | G/T | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007612 | CTTTTTTTTTTTTTT[G/T]GAGATGGACTCTCGC | 9051 |
rs78227498 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997351 | CACTGAGTCTGGGCC[A/G]ATGCCCCGAAAGGTC | 9051 |
rs78282498 | snp | A/G | 0.0062403 | 0.0555087 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77030597 | GTGAGTGGCCCACGT[A/G]GAGCCTCGTTTTCCC | 9051 |
rs78497811 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023709 | GGTGAGGGCGGGGAA[A/G]TGGATGTGCAGGCCC | 9051 |
rs78540067 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013918 | CCTCTGGTGGAGGAA[C/G]GTGTGTAGGGCGAGA | 9051 |
rs78712904 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023032 | CTGGCAGTGCTGTAC[A/G]TTCAGGCAGGCTCCC | 9051 |
rs78797703 | in-del | -/TT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007611 | ACTTTTTTTTTTTTT[-/TT]GAGATGGACTCTCGC | 9051 |
rs78822902 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993790 | GTGGTGCCATTGGGA[C/G]GTGAGGTGCAGCCTG | 9051 |
rs78841980 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004535 | GAGAGTGACCAAGGT[A/G]GAGAGTAGTTGGAGA | 9051 |
rs78843312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021038 | ATTCCCTGCCCCTTG[C/T]AGAACGGGCAGGGGA | 9051 |
rs78869273 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007050 | CTCCTCATCATACTC[C/T]CACCCTGGGCATGTG | 9051 |
rs78947529 | snp | C/T | 0.00482417 | 0.0488755 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018104 | GGCTGTGCTCAGTGT[C/T]GCCTGGTCGTGGCCC | 9051 |
rs79040250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001630 | GCACCTGCCTGGCTG[C/T]ATCTGTCAGAAGCAG | 9051 |
rs79243436 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017946 | GTGGGGCTCACTTAT[A/G]TACCTGTCACCTCTG | 9051 |
rs79288253 | snp | A/G | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035770 | CCAGTGTCCCCAGAA[A/G]GGGAGGGGTCTATGT | 9051 |
rs79289903 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004104 | AGGTCAGTATTCTTA[C/T]TCCTGTTTTACAGAG | 9051 |
rs79338487 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009104 | TGGTTAGAGGATTGA[A/G]AGTGGAGACATGCAG | 9051 |
rs79438763 | snp | C/T | 0.0688328 | 0.172286 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018276 | GCAGGCCATGGGGAG[C/T]GCAGGCAGGAAGCAG | 9051 |
rs79637691 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022252 | TGACGCTGGCTCATC[A/G]TGGGCACAGCCTCAG | 9051 |
rs79704510 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013780 | TAGCAGGTAGGAACT[C/T]GGACCAAAACCCAGG | 9051 |
rs79732372 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031551 | CCACAGAGCACCTGC[C/T]CCCTCTGCCGGGGAT | 9051 |
rs79941195 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015499 | GCCACAGGCAGCATT[C/T]GGATGACAGAGGTTG | 9051 |
rs79947345 | in-del | -/TGCAGGCTGGG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019758 | GGGCTGAGGGCCGGG[-/TGCAGGCTGGG]CACAGAGGAGGGCTC | 9051 |
rs79947875 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037462 | CCGAGGCTTCAGCTA[C/T]AGTTGGAGAAGAGGC | 9051 |
rs79978921 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028844 | ATGGACAGGCAGGTC[A/G]GCTGGATCCCCTTTG | 9051 |
rs79985146 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030645 | ACGCCCATCCCTACT[C/T]CAGCTGCTTAAAGGG | 9051 |
rs80135348 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016399 | TGAGGGGTGGGAAGG[A/G]GAGGGCTGCTGGCTG | 9051 |
rs80152051 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028812 | TGAAATGGGTTTCCT[A/G]GAGAGAACCTCAGGC | 9051 |
rs80227391 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015287 | TGGCTTTGGGGACAG[A/G]TTGACCTGCATTCAG | 9051 |
rs80246505 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001011 | CTCCATCGGGAACAC[C/T]TGTGGGTGTGGACAT | 9051 |
rs80302493 | snp | C/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000847 | TGCACGGCCCTCCCT[C/T]CTTTTTTTTTCTAGT | 9051 |
rs104895417 | in-del | -/GT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031311 | GGTGTGGGGTAAGGT[-/GT]AGGGCAGCCTCTAGG | 9051 |
rs104895418 | snp | A/C/G | 0.000390038 | 0.0139602 | PSTPIP1 | 15 | allele_origin=G(germline)/A(unknown) | 15:77032352 | ATAGACGCCGACATC[A/C/G]ACAGTTTCATCCAGG | 9051 |
rs111227352 | snp | C/T | 0 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023791 | GGAGGGTGGTGTGCG[C/T]AAGGGCTGGGTTGGG | 9051 |
rs111394938 | snp | G/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013409 | CTGGGGTCTCCATGG[G/T]GGGGTGGTGGGGCAC | 9051 |
rs111457547 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008961 | GCCATCTTTGTCTCT[C/T]ACTCTGACCTTGGAG | 9051 |
rs111554178 | in-del | -/AGATATATAT | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000459 | TGGGCATTTAAAGAG[-/AGATATATAT]ATATATATACACACA | 9051 |
rs111644078 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997046 | GGCCTGCCTTCCCTA[C/G]GGCAGAGCTGGGCAA | 9051 |
rs111668455 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034050 | ATTAGAGAGAGAGAG[A/G]GAGATGTCCTGCAGG | 9051 |
rs111872263 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037431 | AGGAGCCTGGATGTG[A/G]AGCTCCCCAACTCAG | 9051 |
rs111963880 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997130 | GCAGGGTATGGCAGC[A/C]GCAGCAGAAGCAAGC | 9051 |
rs111997480 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026734 | GGTTCTGAGCAGACA[A/G]GGGGTCCCCAGAAGC | 9051 |
rs112000861 | snp | C/T | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999200 | GGTACTGGCTGAGGA[C/T]GTGTTCATAGAATAA | 9051 |
rs112012370 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026444 | GTCACAACTGAGCCT[C/T]GAAGGGGAAGAAGCT | 9051 |
rs112022434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031094 | GGGCTGGCCTGGTCA[A/G]CTCCGGCTGAGCTGT | 9051 |
rs112070036 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018779 | ATCCATCCTCAGTCA[C/T]TTGCAGCGCAGTCTG | 9051 |
rs112105697 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030250 | GATGCCCAGAGGCCA[A/G]TACTCTGGACTTGCA | 9051 |
rs112167439 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001532 | GGAGTGGCCCTGGTG[C/T]ACTCAGAGCTTGCAG | 9051 |
rs112173800 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013020 | CTCAGCCCTTCCTAC[C/T]TCAGGTTTTCAGTCC | 9051 |
rs112209688 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999283 | TTTACTTCATTTCAC[-/T]TTTTTTTTTTTTTGA | 9051 |
rs112256546 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029745 | TGTGTTCCCCCATTC[A/G]CCAGCCCTTCTTGGC | 9051 |
rs112266035 | snp | A/G | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999431 | TTACAGACGTGCGCC[A/G]CCACGTCTGTCTAAT | 9051 |
rs112459298 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025066 | ATTGCAGAGGGTTGA[C/T]TGCTTTAATTTGCAG | 9051 |
rs112701383 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003726 | TCACCCACACTTGCT[A/G]GGTGGCCTTGGAGAA | 9051 |
rs112719973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014480 | TGACCTGTGGCCTAC[A/G]CTAACAGGACTGTGC | 9051 |
rs112736225 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996407 | CTGCCCCTCAGCTCT[A/G]GCTGTGCCCAGGGCT | 9051 |
rs112875317 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995756 | ATTGTCATGGAGGTG[G/T]CCCAGGCCCCCACCC | 9051 |
rs112919436 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027138 | TGTGTGTGAGTGCCT[A/G]TGCCTCGCTGGTCTC | 9051 |
rs113013219 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017948 | GGGGCTCACTTATGT[A/C]CCTGTCACCTCTGCA | 9051 |
rs113031269 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996090 | CATTGGATCAGCAAG[A/G]GGATCCAAGGCACTA | 9051 |
rs113044834 | snp | G/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999240 | CAGTGAATGTCTCCA[G/T]GGTCCATCTCCCTTC | 9051 |
rs113150381 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997051 | GCCTTCCCTAGGGCA[C/G]AGCTGGGCAAGGAGC | 9051 |
rs113192593 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010113 | ACCCCCAAGGGCCCA[C/T]GGCCTCCCTTCCTCA | 9051 |
rs113262942 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034225 | GCAGCACAATGGCTC[A/G]GCAAGCCCTGCACCC | 9051 |
rs113351534 | snp | C/G | 0.084364 | 0.187256 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037730 | GGAGGACTCAGTTTG[C/G]AAACAGGAAGCTGGT | 9051 |
rs113386299 | snp | A/G | 0.00869088 | 0.0653445 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77018523 | GGCAGGTGGCCAGAC[A/G]GAGATCAAGTAAGAT | 9051 |
rs113387304 | snp | A/G | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033819 | ACCCGTGCTTAGAGA[A/G]GGCACACACACACCC | 9051 |
rs113414768 | snp | A/G | 0.5 | 0 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037719 | CAGGAATATTCGGAG[A/G]ACTCAGTTTGGAAAC | 9051 |
rs113421352 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028070 | CACCAGCCTGCGGGG[C/T]GCTTGGGCCCGTGCT | 9051 |
rs113450402 | snp | C/G | 0 | 0 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024460 | TCATGAGGCCATATG[C/G]CCGCCAGGGGGCAGC | 9051 |
rs113475295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003058 | AGGAAGGGAAGGCAC[A/G]AGCTGGATTGTGAAA | 9051 |
rs113554225 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036793 | TGCTCCAGTCACTGC[A/G]TCTCCAGAATGGGAG | 9051 |
rs113570193 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010015 | GAAGACGCCTGGACC[C/T]CTCCTGGCTGGCTAC | 9051 |
rs113599218 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030837 | CCAAAACTGGGACTT[A/G]GACTAAACCCACAGC | 9051 |
rs113687128 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000003 | CAGTGACTGTCACCC[A/C]CCCTTTGGGTGGGAA | 9051 |
rs113715427 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012763 | AGAAGTAGAGGGGAC[A/C]AGTGTGACTGGCTTC | 9051 |
rs113749761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023406 | GGCGGAGGGGCAGAG[A/G]GCAGGGCTGACAGGT | 9051 |
rs113774090 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031899 | TTGTTGTTTTTGCCC[A/G]AGTGACTCGAGCCCC | 9051 |
rs113807864 | snp | A/C | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014956 | CTCAAGTGAGCCTCC[A/C]AGAGGAAGAGACTGT | 9051 |
rs113840225 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012209 | TGTCCATCCATCCAT[C/T]CGTCCACCCATCTGT | 9051 |
rs113928004 | snp | A/G | 0 | 0 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995278 | GTGTCCTCCATCACC[A/G]CAGGGTCGGTGAGGG | 9051 |
rs113958561 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010215 | TTGGCAGGGGCGGTA[C/T]AGAGCTGTGTAACCT | 9051 |
rs113987301 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998759 | TCCTGTCCCTCAGTC[A/G]GCCTGTTTTTGCAAT | 9051 |
rs113989057 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026671 | GTAGCGTGGCTGCCC[A/G]TGCCACCTGCCCATC | 9051 |
rs114061633 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030145 | AGTTGTGACCCAAGC[C/T]TGTGGGACTCCACCC | 9051 |
rs114069352 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013573 | AGTCCCTGACCACTC[C/T]GTTCCCTACAGCCTT | 9051 |
rs114092344 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009905 | GGCAATGCCTGGGGA[C/T]GGGGATGTGCAATGA | 9051 |
rs114132480 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993162 | GTAACTGAGGTGGTC[C/T]GTGTGAAAAGCAGAA | 9051 |
rs114245955 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995810 | ACTCCGTGAATGAGC[A/G/T]TCCTCCTCTCTGCTG | 9051 |
rs114248616 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031052 | CCCCAGGGCACTCTC[C/T]CCTTTGGACTGGGCT | 9051 |
rs114328863 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010353 | GAGAGCCCCACCAGG[C/T]ACCGCACACTCAATC | 9051 |
rs114363839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027095 | GTGTCCTTGTCCAGC[C/T]CTGTGCACTTGGGTG | 9051 |
rs114366335 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035739 | AGAAACCCCATTCTA[A/G]TAGGACTTCCAGGGG | 9051 |
rs114434525 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018980 | CCCCCCAGCTGTCTG[A/C]CCATGGGCTGGCTGC | 9051 |
rs114447118 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998930 | ACACAGATGATAAAG[A/G]GCATCACACCTTGGC | 9051 |
rs114457774 | snp | C/G/T | 0.00597646 | 0.0543919 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035213 | ATGAAGCTACAGCTT[C/G/T]GGGGGTTCTAGGATC | 9051 |
rs114461255 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029373 | TGGTCCTCTGTGGGC[A/G]GAGGTTGCTTGTGGA | 9051 |
rs114657901 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020159 | GGGAGCAGGGTGGGC[A/C]TCAGGAAGCAGGAGG | 9051 |
rs114667518 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006684 | TCCAGTTTTCCCAGC[A/G]CCATTTGTTGAAGTC | 9051 |
rs114697446 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000926 | ATCTTAACCATTTTT[G/T]TGGTGTATGGTTCAG | 9051 |
rs114772418 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026279 | TGGCCTGGAGGCTGG[A/G]CTTGGGCCTGTGAGG | 9051 |
rs114778900 | snp | G/T | 0.43978 | 0.162738 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020881 | TGTGGGGGGGGGGGG[G/T]GTGTGTGTTGGCCCT | 9051 |
rs114792045 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008142 | GAGCTGCAGTGAATA[C/T]TAAACGCAGCCAGGT | 9051 |
rs114796733 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995952 | TCACAGATTTAGAGA[C/T]CAGACAAACTTGAGT | 9051 |
rs114883494 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001061 | ACACCACTGTTCATG[A/G]CTGCACAGTTCTCTA | 9051 |
rs114889865 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019528 | GGAAGGCTTAGATGT[A/G]GCATGAGCCGTGTGT | 9051 |
rs114920536 | snp | A/C | 0.0566069 | 0.158427 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993711 | TCCAGACCTAGAGGC[A/C]TCATCCCATCTGATG | 9051 |
rs115011780 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997838 | TGGCCACAGGTGTTA[C/T]ATTAGGAACAGCCCA | 9051 |
rs115282433 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998643 | AGGACGTTTCACAGG[C/T]AGCTAGCAGCCTGAT | 9051 |
rs115284761 | snp | C/T | 0.349013 | 0.229557 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034495 | CCCCCCACAGGCCCC[C/T]GAGTCATGGCTCAGC | 9051 |
rs115368425 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035630 | AGAGGTCTCCCACAT[A/G]GCACAGATGGGGCCA | 9051 |
rs115515528 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028939 | TGAGAGCAGACGCCA[A/G]CCCTCACACAACCTT | 9051 |
rs115515761 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012958 | GTAGGCACCAGGTGC[C/T]GGGATCCAGTGGGGA | 9051 |
rs115531138 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006955 | GCTGCTTTTGTTGTT[C/T]CCTTTTTATAGGTGA | 9051 |
rs115573927 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015417 | GGTCAGGAAGATAAC[A/G]CTATGATACCCTTGG | 9051 |
rs115603767 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000962 | CTAGGTTTGTTCACA[C/G]TTTGCCACCCTCCCC | 9051 |
rs115670384 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029380 | CTGTGGGCGGAGGTT[G/T]CTTGTGGATGATGGC | 9051 |
rs115730377 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016064 | AAGGGTTCCCTTGGC[A/G]TCAGGGCTGGGTGTG | 9051 |
rs115845814 | snp | A/C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994970 | CTCAAGCTCCCTTAG[A/C/T]ATATGGCCTCTGGAA | 9051 |
rs115847788 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025724 | CAGGGGTGGTGGTGG[C/G]ACAGCACTCCAGGCT | 9051 |
rs115864060 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010654 | CTTCTCTTTTCTATT[C/T]CTTTTTCTTTTGAGA | 9051 |
rs115864145 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026540 | TCAGTTTCCCTCTCA[C/T]AGGATGGGACACATA | 9051 |
rs115902547 | snp | A/C | 0.0501905 | 0.150254 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017561 | GCCCACAGAGAGCCC[A/C]GCGCAGCATCTGGCA | 9051 |
rs115915277 | snp | C/T | 0.0562307 | 0.157967 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993957 | CCTTCTGGGGGCAGT[C/T]CCATTGCTCTGCAAT | 9051 |
rs115916890 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009886 | GGCGTAGGTGGTGTG[A/G]GAGGGCAATGCCTGG | 9051 |
rs115981590 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037620 | CAGGCTTCTTGGGGG[C/T]GGAGGGTTGAGCAGG | 9051 |
rs116030720 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997478 | GAAAGATGTGCCAGG[C/T]GCTGTTCTCAAGATG | 9051 |
rs116035834 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021824 | TGCTCCCCTGCCCAG[C/T]CCCACCCATCCCTCA | 9051 |
rs116141662 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998639 | CGAAAGGACGTTTCA[C/T]AGGCAGCTAGCAGCC | 9051 |
rs116142711 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029715 | ATTCCAGATATGTGC[C/T]GTCAAAGTAAACGCT | 9051 |
rs116236275 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999661 | CTGGACCCCTGAGCT[G/T]CTTCACCCTGCAACA | 9051 |
rs116237318 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036370 | TGCCTTTGGGTCAGG[A/G]CCCTGTCCTTCGTGG | 9051 |
rs116398198 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009874 | ACATCCCTGGCAGGC[A/G]TAGGTGGTGTGGGAG | 9051 |
rs116634004 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001470 | TGGAAGGCCTTGCAG[C/T]CCAGCAAACTGCTGT | 9051 |
rs116638927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030090 | ACTCAGCTACTCCCT[C/T]GGCTGGGGGACAGGT | 9051 |
rs116799868 | snp | C/G/T | 0.0158469 | 0.0875917 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036973 | TGCTGGGTGGGGGAA[C/G/T]GCCAGGCCCCTCCCT | 9051 |
rs116827184 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996024 | TCTCCAAGCCTCAGT[A/C]TCTCCATCTATATAA | 9051 |
rs116828533 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027232 | CTCATAACCCAGTCG[C/T]TGTCCTGGCTGTTTT | 9051 |
rs116860971 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994236 | CCGGCAGGGCGTGGC[A/G]TCTCAGGGCTGGGGC | 9051 |
rs116894585 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032032 | GTCACTCTCCTCTGA[A/G]TTTCCTCATCTATCC | 9051 |
rs116895455 | snp | A/C/G | 0.015169 | 0.0857636 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032439 | TCTAGGTGCATTGAG[A/C/G]CCCTGGGAAGGCCCG | 9051 |
rs116992402 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015811 | CCTGGAGAGTCAGGC[A/T]CTTCCTCGGAACATC | 9051 |
rs117080115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036697 | GCTGGGGCTGGGGAC[C/T]GCAAAGGGGAGGCTT | 9051 |
rs117147776 | snp | C/T | 0.00074239 | 0.0192521 | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994845 | AATGACTTGCTAGTG[C/T]GGGGTGGGGAGTCTG | 9051 |
rs117273013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023924 | GGTGAGGAGTCAGAG[A/G]AGAGTCCTGAGCCCC | 9051 |
rs117378779 | snp | A/G | 0.0633504 | 0.166319 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037227 | AGTGGAGCCAGCAGT[A/G]CCCCCAGCACTGTCC | 9051 |
rs117481034 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016194 | CATTTCCTTCTCTGG[C/T]CTCAGTTTCCTGAGG | 9051 |
rs117490796 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016864 | CCTCACACCCCTAAG[G/T]TGGCATTTGAGGGGA | 9051 |
rs117563900 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, splice-donor-variant | PSTPIP1 | GRCh38.p7 | 15:77024532 | ATACTGGATGCCCAG[A/G]TGAACGTGAATTTCA | 9051 |
rs117578733 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004395 | ACCAGCAGCCAGTGT[A/G]GGGATGTGGTGGCCA | 9051 |
rs117606006 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022713 | CCTCCTTGAAATTTC[A/G]TCTGGGGCCAAGAAA | 9051 |
rs117656395 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033319 | GGGGCATCTGGAGAA[G/T]TCTCCAGGCTTTTCC | 9051 |
rs117745032 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029690 | GCACAATCATGGGCG[C/T]GGCGCTCTCATTCCA | 9051 |
rs117798384 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037621 | AGGCTTCTTGGGGGC[A/G]GAGGGTTGAGCAGGT | 9051 |
rs117912248 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016863 | CCCTCACACCCCTAA[G/T]GTGGCATTTGAGGGG | 9051 |
rs118055752 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037476 | ATAGTTGGAGAAGAG[A/G]CCTGGCCCCAGTTGC | 9051 |
rs118083575 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018013 | CCAGGTCTGGAGTCC[C/T]AAGAGCTTGCCCTGA | 9051 |
rs118109987 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023581 | ATAGCTGGTGGACAG[C/T]GGTGTCTTTGCCAAG | 9051 |
rs118156980 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017052 | GAAGACAGACTAGGT[A/G]CGGAATGTCAGGCCT | 9051 |
rs121908130 | snp | A/G | | | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031225 | ACCATTCTCCGCAAC[A/G]CCCTGTGGGTGCACA | 9051 |
rs137952261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033304 | GGCTGGAGCAGGACT[A/G]GGGCATCTGGAGAAT | 9051 |
rs137965147 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000291 | TTCCCAGTTCTGAGA[C/T]GCTGAGGTGCCCATT | 9051 |
rs138005112 | in-del | -/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993622 | TAGAGAGGCAGGGCA[-/G]GGGAGCCCAGCTGTA | 9051 |
rs138021447 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030285 | TGAGGCTCCACTCCA[G/T]CCCTCAGGCAGCTCA | 9051 |
rs138056015 | snp | A/G | 0.000168005 | 0.00916375 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037086 | GGGAGACATCCTGGA[A/G]GTGATCCTGGAAGGG | 9051 |
rs138060054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009992 | GCAAGGAGCCGTGCT[C/T]TTCCTGTGAAGACGC | 9051 |
rs138108416 | snp | C/G | 0.489201 | 0.0726845 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034202 | GGGGAAAAGAGGTGT[C/G]GGGGCACGCAGCACA | 9051 |
rs138190798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018416 | CCTCCCCCAGAGGTG[A/G]CAAGTCACTGATGAT | 9051 |
rs138217389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019805 | TGGTGAGGAGTGAAT[C/G]GACGTATGCAGGGAG | 9051 |
rs138285076 | in-del | -/TCCC | 0.260227 | 0.249791 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024727 | GCAGTGCTGGGCCCT[-/TCCC]TCCCTCCCTCCCTCC | 9051 |
rs138313338 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000857 | TCCCTCCTTTTTTTT[-/T]CTAGTATTTTAAATT | 9051 |
rs138332929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025856 | TGTCGAGCTGCCTCA[C/T]GCCTAGGAGGATCCT | 9051 |
rs138560535 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999698 | CAGATGAATGAAACT[A/G]TCTTGACCTGAAGGA | 9051 |
rs138576564 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006622 | TGAGTTAATTTTTGC[A/G]TATGGTATAAAGTAA | 9051 |
rs138719117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003269 | GGAAACCAAGACTGC[C/T]TCTGCTTCCAGCTAG | 9051 |
rs138849580 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025184 | GGTCTTCCCACCAAA[A/C]TAAAAGTCCTCCCCA | 9051 |
rs138895822 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010072 | GGGTCTGGGGTGGCT[C/T]AGCTCCATCCTCCCC | 9051 |
rs138933292 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014277 | AGCCCTGATCTTGAG[G/T]CCACTGTTCTCACCT | 9051 |
rs138937060 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002616 | GCCCATTCCACAGGA[C/T]GTGGCCGGCTGCTCA | 9051 |
rs138986244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020488 | AAGTACTGTTGATGA[C/G]GCCATGCAGCTGTTC | 9051 |
rs139056263 | in-del | -/AT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000503 | CACACACACACACAC[-/AT]ACACACACACACTTT | 9051 |
rs139058976 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016512 | CGCCTGCCTCTGAGG[C/T]TGGGGGGACAGCTTC | 9051 |
rs139143352 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993643 | CCCAGCTGTAAAAAT[C/T]TCTGCCAATAAGCAG | 9051 |
rs139152275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010377 | CTCAATCCCTTCCCC[G/T]GAACCTGGAACCTGG | 9051 |
rs139180217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003651 | AAAGAACGAAACTCC[A/G]TCTCAAAAAAAAAAA | 9051 |
rs139298465 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034673 | CACCTGCAGTGCCTC[A/G]CTCCCCCTTCTCTCC | 9051 |
rs139351566 | snp | C/T | 7.93871e-05 | 0.00629978 | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032862 | GCTTGCTGTCTGCAG[C/T]TCCGGTGCCCTACCA | 9051 |
rs139362350 | snp | A/C/G | 0.00148737 | 0.0272316 | missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031194 | GGCCTTTCAGCTGCA[A/C/G]GAGTTTGACCGGCTG | 9051 |
rs139372275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011299 | TCCCTTCAGTGGGAC[C/T]CCTGGGAGTCCCTGG | 9051 |
rs139457876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021666 | CCTGGGCTGCAGAGC[A/G]AGACTCCATCTTAAA | 9051 |
rs139529282 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026542 | AGTTTCCCTCTCACA[C/G]GATGGGACACATATG | 9051 |
rs139552419 | snp | C/G | 0.00148835 | 0.0272389 | PSTPIP1 | 15 | allele_origin=G(germline)/C(germline) | 15:77035569 | GCTTCTGCTGGTAAA[C/G]GGGGTCAGGAGGGGA | 9051 |
rs139563119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026835 | ACCTGCCAGGAAGGA[A/G]GGACCCCGGCCCTGC | 9051 |
rs139726858 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036109 | ACACTAGCAAGGGTA[C/T]CTGGGAGTGTGCTTG | 9051 |
rs139903276 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007884 | CAAGTGTGAGCCACC[A/G]CGCCCGACTGGCAAT | 9051 |
rs139918038 | in-del | -/AG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034038 | GCCCCAGAGAGGATT[-/AG]AGAGAGAGAGAGAGA | 9051 |
rs139957287 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997707 | GCTTCGGGGTAAGAT[A/G]AGAGGTAACCCCTCT | 9051 |
rs140166252 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012160 | CCATCCATCCATCCA[C/T]CCACCCACCCACCCA | 9051 |
rs140185335 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015893 | AAGCTCTGAGCGGGG[G/T]ACTGGGCGGGATCCT | 9051 |
rs140228501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012555 | TCCATCCATCAAGTT[G/T]TACCTGAGTGTTTGG | 9051 |
rs140418293 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014664 | AAAGGGGGAAGTGGC[-/G]GGTAGTTACAGAGGG | 9051 |
rs140453624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018709 | AGGTTCTGTGAGGGA[A/G]GAAGCCCGAGGGTCT | 9051 |
rs140481947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001019 | GGAACACCTGTGGGT[A/G]TGGACATGGGTTCCT | 9051 |
rs140508596 | in-del | -/G | 0.00810961 | 0.0631588 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029495 | CTGGCTCCTGGGGCA[-/G]GGGCTTAGCGCTGCT | 9051 |
rs140508674 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031947 | CCTTGAGGTAGAAGG[A/G]CGAGCTCTGGACCCA | 9051 |
rs140549078 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994107 | CTCATCTTATCACCC[C/T]GTCAGCTGTAAGGCA | 9051 |
rs140579815 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004580 | GAACAGTGGCCAGGC[A/G]TGGTGGCTCACACCT | 9051 |
rs140661993 | snp | C/G/T | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994619 | TTGCGGTGGTGGCGG[C/G/T]GGTGGTGGTGGGGGC | 9051 |
rs140787369 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008359 | TCCCCGTCCTCAGAT[A/G]ACTCCCAGTCCTCAA | 9051 |
rs140796422 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005792 | TAATGTCTTCAAGGC[C/T]CATCCATGTCATAGC | 9051 |
rs140835757 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009097 | ACTTTGGTGGTTAGA[G/T]GATTGAGAGTGGAGA | 9051 |
rs140840189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013674 | CTGTCAGGCTATTCT[A/C]ATGGACAGAATTACC | 9051 |
rs140930550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998448 | AAAGCTCATATACTA[C/T]ACTCCTAGGAGATGT | 9051 |
rs140933380 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023452 | TGCGGCAGGGGCTGC[A/G]GCGGTGGTGGCAGCT | 9051 |
rs141032908 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028795 | CCCAATCTCCCCATC[G/T]GTGAAATGGGTTTCC | 9051 |
rs141140239 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000245 | GTCTGCCCCTTCCCT[A/G]TGTGGCACTCAGCCA | 9051 |
rs141227274 | snp | C/T | 0.00274886 | 0.0369713 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037068 | TGAGCTGGACCTGTC[C/T]GCGGGAGACATCCTG | 9051 |
rs141236252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027103 | GTCCAGCCCTGTGCA[C/T]TTGGGTGTTTTGTGC | 9051 |
rs141282975 | in-del | -/C | 0.0310518 | 0.120672 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023969 | GTCACCACACAGCCA[-/C]CCCCTCTCCTTCTTC | 9051 |
rs141331888 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017813 | GTGAATTTCAGGCCT[A/G]GCTGTCATCAGGGGG | 9051 |
rs141519847 | snp | C/G | | | upstream-variant-2KB, intron-variant | PSTPIP1 | GRCh38.p7 | 15:76994992 | CCTCTGGAATAAAGT[C/G]AGCCCGCACCTCGGG | 9051 |
rs141616584 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033349 | CAGGGCTCCTTCCCC[A/G]GCCTGGCTGCAGTCA | 9051 |
rs141632112 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021490 | TCGAGACCAGCCTGG[C/T]CAACATGGTGAAACC | 9051 |
rs141744477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036381 | CAGGGCCCTGTCCTT[C/T]GTGGCCATGGGTGTG | 9051 |
rs141764641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007625 | TTTGAGATGGACTCT[C/T]GCTCTGCTGCCCAAG | 9051 |
rs141814002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033153 | CCCAAGGGACCCAGA[C/T]ACTAGAATAATCACA | 9051 |
rs141956863 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015488 | CAAAGGGCAGGGCCA[A/C]AGGCAGCATTCGGAT | 9051 |
rs142130132 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020717 | ATTTATGCGCCACCT[C/G]CTCCAGGAAGCCCTC | 9051 |
rs142149106 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031026 | GGGCTGGCCCGGAGT[C/T]GGGATGGGGACCCCA | 9051 |
rs142169486 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993314 | ATTGCAGAGTCTCTC[C/T]AGAGGTTCCTCACAT | 9051 |
rs142171021 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025530 | AGCTCACACATCCAG[C/T]TGGCCCTGACCCTGC | 9051 |
rs142263583 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000945 | TGTATGGTTCAGTAG[C/T]GCTAGGTTTGTTCAC | 9051 |
rs142373986 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037714 | ACACCCAGGAATATT[C/T]GGAGGACTCAGTTTG | 9051 |
rs142415251 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003030 | GCCCAGAGCATTGTG[C/T]AAGGTGACTGGTAGG | 9051 |
rs142537104 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001746 | ACCTGGTCGGCAACC[C/T]GTTGTGAAAAGTGGG | 9051 |
rs142544259 | snp | A/G | 8.4533e-05 | 0.00650072 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037108 | CTGGAAGGGGAGGAT[A/G]GCTGGTGGACTGTGG | 9051 |
rs142600282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999810 | CATCCTCTCCCAGGT[C/T]CCCCATCCCCCGCAA | 9051 |
rs142688454 | snp | C/T | 0.00092584 | 0.0214956 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026147 | GACAGAGTGACTGCA[C/T]GGAAGTGAAGTCCCC | 9051 |
rs142709708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029958 | CTCTGTCCTTCACTT[A/G]ATGCCCGAATCCTAC | 9051 |
rs142915442 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013610 | CCAACCTCTCCCGTT[-/G]CACCCAATAGTCTGC | 9051 |
rs142999123 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008916 | GGGCGATTTCCCAGA[C/T]TCCAACATAGAAGCC | 9051 |
rs143004123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036792 | ATGCTCCAGTCACTG[C/T]GTCTCCAGAATGGGA | 9051 |
rs143326445 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032740 | TGGGAGCAAGACAGG[C/T]ACCTCCTCAGGCACC | 9051 |
rs143384492 | in-del | -/CCCCCCCCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033626 | GTGCCTGTGCCCCCA[-/CCCCCCCCC]CCGCCATGCCACCAC | 9051 |
rs143431766 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002821 | CCAGTCCCCTGGAAC[C/G]CACATGCTTTTCCTG | 9051 |
rs143432050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996243 | TTCTTAAATTCAACA[C/T]GGGCTTAAATCAAGT | 9051 |
rs143476906 | in-del | -/CTC | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036024 | CTTGCGTCCTCATCT[-/CTC]CTCATGGTTTCACTC | 9051 |
rs143524873 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000645 | TGCTGTGTTTGCATA[A/G/T]GATTGCCTTACATAG | 9051 |
rs143536570 | in-del | -/GG/GGG | 0.00827 | 0.0638684 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035611 | AAACACACTGATCCT[-/GG/GGG]GGGGGGGAGGAGAGG | 9051 |
rs143603046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031470 | AGTACCACACAGGGC[C/T]ATGGCTTCTCTGCCT | 9051 |
rs143659491 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023389 | GGCACCTGGAAGCAA[C/T]GGGCGGAGGGGCAGA | 9051 |
rs143704507 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027642 | GCAGCAAGGACCTCA[C/G]GGCACACCCATGCCC | 9051 |
rs143822160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008150 | GTGAATACTAAACGC[A/G]GCCAGGTGTGAGGTC | 9051 |
rs143856596 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010100 | CCCTGCATCAGTCAC[C/T]CCCAAGGGCCCACGG | 9051 |
rs143940023 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016122 | AGGTATCAGGAAGGA[A/G]TGACAGGTCCCCTGA | 9051 |
rs143948003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996475 | GAATGTGGCTGTCCC[A/G]GGGTGCTGCCTCCAA | 9051 |
rs143948509 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030758 | GCCCTGTTGCTTGTC[A/G]CCTGGCCTTGAGTCC | 9051 |
rs144174583 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034693 | CCCTTCTCTCCTAGT[A/G]AAGCTTCACTCATCT | 9051 |
rs144204462 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997712 | GGGGTAAGATAAGAG[A/G]TAACCCCTCTTATCT | 9051 |
rs144206825 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037352 | GTGTGCTGGGGTCCC[A/G]TTCTCTTTTTCTCCT | 9051 |
rs144356705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022066 | AGTTTGAATCCTCAC[A/G]TCCCTGCCTCACCCC | 9051 |
rs144389829 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026050 | CTGAGGGGTCAGACA[C/T]AGACTGGGGTGGGAG | 9051 |
rs144421314 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017275 | TCCCCCAACTTCTCA[C/T]ACCCAGCTTCCCACA | 9051 |
rs144495395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76997070 | TGGGCAAGGAGCAGC[A/C]TCCATGGCAGGATCT | 9051 |
rs144527688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034656 | GCCCTCCCTCTCCTG[A/G]TCACCTGCAGTGCCT | 9051 |
rs144577744 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009292 | GGGTCCCTGCCTTCA[A/C]GGAAGGGCACGGGCA | 9051 |
rs144652154 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003704 | TCTTTGAAGCCTCAC[C/T]CAACCCTCACCCACA | 9051 |
rs144702485 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006200 | ATCGTAGTTTTGATT[G/T]GCATTTCTCTAATAA | 9051 |
rs144714026 | snp | C/G | 0.0107246 | 0.0724382 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037758 | GGTGATGGATCTGTT[C/G]GAGAGGCCATGGTGG | 9051 |
rs144789153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004504 | GCTGAGGCAAGAGCA[G/T]GCCTGCGTGGCTAGA | 9051 |
rs144825829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008656 | CTCAGGTAATCCACC[C/T]GCCTCGGCTTTCCAA | 9051 |
rs144836609 | in-del | -/TGTCCACC | 0.0217236 | 0.101931 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012334 | ACCCATCCCTCCATT[-/TGTCCACC]TGTCCACCAGTCCAC | 9051 |
rs144914003 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005374 | CTGGGCAACAAGAGC[A/G]AACACTCAATATCAA | 9051 |
rs144959782 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016788 | CTTCTCCTTCCAGCA[C/T]CTGACTCAAATGCCT | 9051 |
rs144960304 | snp | C/G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027224 | CCTCCTACCTCATAA[C/G/T]CCAGTCGCTGTCCTG | 9051 |
rs145048662 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020248 | GGCCCTGATTGCGCC[A/T]TGGTTATTCAAGGCC | 9051 |
rs145074031 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024326 | CTGGATCCCCAGGCT[C/T]CTGCCAGGCTACTGC | 9051 |
rs145114353 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023204 | GACAATGAGGAGGAG[A/G]GCCAGGCATTGCCCC | 9051 |
rs145198321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022190 | TGACGACATTGCTGA[A/G]GATATTGGCGGGAGA | 9051 |
rs145239831 | snp | A/G | 0.00111861 | 0.0236231 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032355 | GACGCCGACATCGAC[A/G]GTTTCATCCAGGCCA | 9051 |
rs145344175 | snp | A/G/T | 0.00249754 | 0.0352505 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037069 | GAGCTGGACCTGTCC[A/G/T]CGGGAGACATCCTGG | 9051 |
rs145555071 | snp | A/G/T | 0.00597678 | 0.0543977 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001240 | CTTTGGGCAGAGGAG[A/G/T]CTAATGGCTATTTTC | 9051 |
rs145605526 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026952 | CCCCGCAGGCAGAGC[A/G]CTGTGTTGTAGTGTG | 9051 |
rs145620539 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994148 | AGGGTGGTGATTTGC[A/G]GACAATCCCTGACTC | 9051 |
rs145748718 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998841 | CCGAGTGTTCAGATG[C/T]ACGCTGCTGTAGGAG | 9051 |
rs145750201 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025707 | GAGCCAGTGGAGGGC[A/G]GCAGGGGTGGTGGTG | 9051 |
rs145792758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008676 | CGGCTTTCCAAAGTG[C/T]TGGGATTACAGGCGT | 9051 |
rs145871454 | in-del | -/AC | 0.0158469 | 0.0875917 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037517 | CAGACTGCCAAGGAG[-/AC]ACATTCACACCTGGA | 9051 |
rs145985493 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000390 | CCCAGACCTGTCTAC[C/T]ATGGCCCAGGGGCAT | 9051 |
rs146024481 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035393 | AGGCTAGGGGCAGTC[C/G]CAGCCCTGGCAGAGC | 9051 |
rs146035424 | snp | C/T | 0.001926 | 0.0309725 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77037131 | GACTGTGGAGAGGAA[C/T]GGGCAGCGTGGCTTC | 9051 |
rs146035496 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997678 | GTCTATCTGACATAT[A/C]ACTGGATCTTTTGGC | 9051 |
rs146236077 | in-del | -/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015048 | CCGTGACCACTGGCT[-/G]GTTCATGGGTTACCC | 9051 |
rs146271206 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000671 | CATAGGTGCAAGCAT[A/G]TTGTGTACATAATTT | 9051 |
rs146511416 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993803 | GAGGTGAGGTGCAGC[A/C]TGGCTCACTCTATGG | 9051 |
rs146534895 | snp | C/T | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998074 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 9051 |
rs146584100 | snp | A/G | 0.0279526 | 0.114869 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994160 | TGCGGACAATCCCTG[A/G]CTCACCCCATTTTGC | 9051 |
rs146652446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012540 | CCATTCATCCATCCA[C/T]CCATCCATCAAGTTG | 9051 |
rs146700856 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009488 | ATTTACAGATGAAAA[A/G]ATTGAGGCCAGAGAG | 9051 |
rs146773249 | in-del | -/AGG | 0.0193772 | 0.0965046 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027632 | CCAAGGTCTGCAGCA[-/AGG]AGGACCTCACGGCAC | 9051 |
rs146799300 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031616 | CAGAAGCTGGAGGAC[C/T]GTGGCTGCTCTGCTC | 9051 |
rs146818403 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027400 | GAGTGGCATCTGTGG[G/T]TGTGCACAGGAATGC | 9051 |
rs146902648 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999843 | TGTATGTCTATCCAA[C/T]GGCCTTTGCAAAGAT | 9051 |
rs146912424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002192 | TGGGACCTAAGGCAC[A/G]GCAGGTCTAGGCCCA | 9051 |
rs147017193 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017949 | GGGCTCACTTATGTA[C/T]CTGTCACCTCTGCAG | 9051 |
rs147111015 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033281 | AGGCTGCAGTGGCAA[C/T]GCTGTCTGGCTGGAG | 9051 |
rs147120840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036382 | AGGGCCCTGTCCTTC[A/G]TGGCCATGGGTGTGG | 9051 |
rs147120980 | snp | C/T | 0.00114536 | 0.0239033 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995457 | GCAGACGGCGCCGGC[C/T]GGGAAGGGGGGCCTG | 9051 |
rs147132158 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996817 | TGCCTCAGCCCATCC[A/G]GAGGACCAGGCACCA | 9051 |
rs147238110 | in-del | -/CTC | 0.223522 | 0.248594 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant, cds-indel | PSTPIP1 | GRCh38.p7 | 15:77037330 | GGAGTGCGTTCTGTT[-/CTC]CTTGGTGTGCTGGGG | 9051 |
rs147277315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008354 | TTTCATCCCCGTCCT[C/T]AGATAACTCCCAGTC | 9051 |
rs147339976 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030006 | CTGGTGCCCCACCCA[C/T]CAGACACAGCACCCA | 9051 |
rs147382403 | snp | A/T | 0.000184519 | 0.0096034 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026196 | GCAGAGGCTGGCAGA[A/T]GCTTGTCAGGGAGGC | 9051 |
rs147688627 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004245 | TGCAGTTAATGGGAG[A/G]GTGTGTTGGTTTGCT | 9051 |
rs147730610 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001303 | GGGCCAGTTCTCCAG[C/T]CATGGGTACTAGCAG | 9051 |
rs147740780 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036419 | GTGGCCAGAATGAGT[C/T]TTGCTATCGTGCCAG | 9051 |
rs147792377 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022144 | TTTAAAATTTTTTTC[A/C]TGGTCTCTCTTCCTC | 9051 |
rs147835091 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017472 | TGTAGGGTGTGCTTG[C/T]GCATGCTCTGACCTG | 9051 |
rs147940914 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036242 | CACAGCACACACGTG[A/G]AGCACATGTACCTAT | 9051 |
rs148008550 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002948 | TGTCAGGAGGACAAA[C/T]GGCACTCAAGGTGGG | 9051 |
rs148060762 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007325 | TAAAAATCAGACTTC[C/T]GGCCCTGTGCAGTGG | 9051 |
rs148104406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015390 | ATCTTCGCCTCCCGA[A/G]ATCTGTGTTGTGGTC | 9051 |
rs148152818 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028090 | GGGCCCGTGCTGGGC[G/T]CTATGGCCCCGTGGG | 9051 |
rs148206609 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000180 | TGACAGCACCGCTGC[C/T]GAGTGGGGCAGTGAC | 9051 |
rs148361080 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon | PSTPIP1 | GRCh38.p7 | 15:76994804 | GATGAATGACAGATG[C/T]CCTAGACCTGGGTAA | 9051 |
rs148506169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004083 | AATTCCAACAATAGT[C/G]CTGTGAGGTCAGTAT | 9051 |
rs148557797 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008752 | AGGCTGAGAGTAAAA[C/T]GTTAAATAGTGAGTG | 9051 |
rs148579343 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021248 | CCACTGAAATTAACA[A/G]GAGGTTACATCTTAA | 9051 |
rs148596145 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013414 | GTCTCCATGGGGGGG[-/T]GGTGGGGCACAGGCC | 9051 |
rs148619462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026104 | CCAAAGGTACTTCTC[A/C]CCCATATGTAGGGCA | 9051 |
rs148680520 | in-del | -/AT/ATAT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000458 | TGGGCATTTAAAGAG[-/AT/ATAT]AGATATATATATATA | 9051 |
rs148714717 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037448 | GCTCCCCAACTCAGC[C/T]GAGGCTTCAGCTATA | 9051 |
rs148989519 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998868 | GGAGTGAGGCAGGGC[A/G]GACCAGCCACAGAGG | 9051 |
rs149036825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036764 | GGTATGATGAGCACC[C/T]GTGACCCCTGACATG | 9051 |
rs149046986 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017124 | CCTCTCAAGCTCCCC[G/T]GGAGTAAGCCTGCGT | 9051 |
rs149099456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023213 | GAGGAGAGCCAGGCA[C/T]TGCCCCTGTCCTCAA | 9051 |
rs149152344 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76994341 | TTCCAGAAATATTCT[C/T]GACACCGTCTACTTT | 9051 |
rs149195362 | snp | C/G/T | 0.00775368 | 0.0617804 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77032393 | GGGCACAGAGCCCCC[C/G/T]GGTGAGGTCCGGCTT | 9051 |
rs149217913 | in-del | -/GGGTGCAGGCT | 0.231775 | 0.249335 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019755 | GAAGGGCTGAGGGCC[-/GGGTGCAGGCT]GGGCACAGAGGAGGG | 9051 |
rs149299105 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034271 | GGCCGCTTCCTCCAC[C/T]TGTCCCCAGCCCCTG | 9051 |
rs149355940 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003666 | GTCTCAAAAAAAAAA[A/G]AAGAAGAAGAAGGAA | 9051 |
rs149504928 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010005 | CTCTTCCTGTGAAGA[C/T]GCCTGGACCCCTCCT | 9051 |
rs149513523 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015099 | AGCCTGGGCCCCAGG[-/T]CTAGCCTCTGTGAAT | 9051 |
rs149515994 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000374 | GCTGCCTGTCCCTAC[A/C]CCCAGACCTGTCTAC | 9051 |
rs149577219 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019937 | CTCCCAGCCTCCAGG[C/T]CAGCTGGAAGAGAAC | 9051 |
rs149651267 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025985 | ATCAGGGCTGATTGT[C/T]CTGGAAAAAGGCAGA | 9051 |
rs149668347 | in-del | -/CTGC/CTGCCTGCCTGC | 0.265001 | 0.273384 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995149 | TGCGCAGGCCTCGGG[-/CTGC/CTGCCTGCCTGC]CTGCCTGCCTGCCTG | 9051 |
rs149757299 | snp | C/G | 0.030278 | 0.119257 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026865 | CTATTTTGGGCCCTC[C/G]TGTGGCCAGAGGAGC | 9051 |
rs149810691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998633 | GGACTACGAAAGGAC[A/G]TTTCACAGGCAGCTA | 9051 |
rs149827453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036205 | CTGGTGTGCAGCAGG[C/T]CTGTGTCTGCCCGGG | 9051 |
rs149869928 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016621 | GGGATGCTTATGGAG[C/G]GGGTAGGAGCTTGGG | 9051 |
rs150133822 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013871 | CAGGCAAGGGAGCAT[C/T]TGAAAAAGGCTCTGC | 9051 |
rs150280393 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029151 | CCAGGAAACACATCA[C/T]TCATTGCACAGACAG | 9051 |
rs150299914 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004883 | AAACAAACAAACAAA[A/C]AAAACAAAGAAAGAA | 9051 |
rs150351857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009816 | GCCTGAGCCCTGTCA[C/T]GCCCCACTGCCTGGA | 9051 |
rs150395070 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019451 | TGCCATACTCTGAAG[G/T]TCCCCCAAAGACACC | 9051 |
rs150404378 | in-del | -/CATCCACC | 0.0733688 | 0.176922 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012270 | ACCTACCCATCCACT[-/CATCCACC]CATCCACCCACCCAT | 9051 |
rs150499039 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021665 | GCCTGGGCTGCAGAG[C/T]GAGACTCCATCTTAA | 9051 |
rs150544547 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033607 | GGGTCTGTGGGTTTC[A/G]CATGGTGCCTGTGCC | 9051 |
rs150588740 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007786 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGGTTA | 9051 |
rs150754542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000261 | TGTGGCACTCAGCCA[C/T]TGGTGCCTTTTCCCT | 9051 |
rs150850150 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011141 | TGGTCAAAAGCCAGA[A/C]GCCCCACAACATTAG | 9051 |
rs150953922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013385 | CCCACACTGCACTGC[C/T]AGCTGCCTCTGGGGT | 9051 |
rs151046609 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023439 | GAGGTGGAGGTGGTG[C/T]GGCAGGGGCTGCAGC | 9051 |
rs151068642 | snp | C/G/T | 0.00366511 | 0.0426524 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035968 | CAAACCCACCTGTGC[C/G/T]ACCTCCCCTGCACCT | 9051 |
rs151185753 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993547 | TGGGAAAGGTGCCTC[C/T]AGGGAGAGGGAAGAG | 9051 |
rs151240315 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012152 | CCATCCATCCATCCA[C/T]CCATCCACCCACCCA | 9051 |
rs151277980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000946 | GTATGGTTCAGTAGC[A/G]CTAGGTTTGTTCACA | 9051 |
rs151331842 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004540 | TGACCAAGGTGGAGA[A/G]TAGTTGGAGATAAGG | 9051 |
rs180730805 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017916 | AGGCCCGGCACCCCC[A/G]GCCCTGTCAGCTGGG | 9051 |
rs180738579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007829 | TCGATCTCCTGACCT[C/T]GTGATCTGCCCGTCT | 9051 |
rs180743125 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997657 | GTGTTGTTGCAGGAT[C/T]CCTCTGTCTATCTGA | 9051 |
rs180767024 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037351 | GGTGTGCTGGGGTCC[C/T]GTTCTCTTTTTCTCC | 9051 |
rs180769125 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026660 | CTGGCAGAAATGTAG[C/T]GTGGCTGCCCGTGCC | 9051 |
rs180896148 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012148 | CCATCCATCCATCCA[C/T]CCATCCATCCACCCA | 9051 |
rs180897374 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022880 | TGCCTGCCCAGGTAC[A/C]CCAGACAGAGGTAGC | 9051 |
rs180899167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002394 | GGATTCTCTCCATCC[C/T]CCATCTAATTTTCTG | 9051 |
rs180899627 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031655 | GTGCTTGCAGGAGCC[A/G]AGGCGCAGTCCTTCC | 9051 |
rs181307808 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022240 | TCAGATGTCCCCTGA[C/T]GCTGGCTCATCGTGG | 9051 |
rs181312648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001948 | TGTTTGATTTTTGAA[C/T]CATATGAATGTATTA | 9051 |
rs181432186 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033060 | GCACCTACTATGTGT[C/G]TGTATCTGGTGCCCA | 9051 |
rs181531465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023096 | AGCTCCCAGAACCTG[C/T]GATTCCTTACAGCAC | 9051 |
rs181568154 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996652 | GGGGCCTGTGGCCAG[C/T]GTGTGAGTGTTCTGC | 9051 |
rs181573901 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013319 | ACTTTCACTGGAAGC[A/C]TCTGATGGGGAAAAG | 9051 |
rs181621668 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028830 | GAGAACCTCAGGCCA[C/T]GGACAGGCAGGTCAG | 9051 |
rs181622780 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012860 | CCTCAGGAAGCAGCC[A/G]TCATAAGGCCTTGTC | 9051 |
rs181726778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017337 | TGCACAGTGAGAAAG[G/T]AGAATTGGGTTGGCC | 9051 |
rs181929438 | snp | A/G | 8.42566e-05 | 0.00649009 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037101 | GGTGATCCTGGAAGG[A/G]GAGGATGGCTGGTGG | 9051 |
rs182012485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009009 | ATCCTACTACACTCA[C/T]GGGTGGTCCTGGGGA | 9051 |
rs182024699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008349 | AGAAATTTCATCCCC[A/G]TCCTCAGATAACTCC | 9051 |
rs182062969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027591 | TGTGTTGGGGTGGGA[A/G]CTCCCCAGCTGGAGA | 9051 |
rs182182930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998948 | ATCACACCTTGGCAG[G/T]AAGTTTGTAAATGAG | 9051 |
rs182225563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013422 | GGGGGGGTGGTGGGG[C/T]ACAGGCCGTGACTGT | 9051 |
rs182230357 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033629 | GCCTGTGCCCCCACC[A/G]CCATGCCACCACTCT | 9051 |
rs182248599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021476 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 9051 |
rs182495316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009795 | TGGCCAGAACCAGAA[A/C]CCAGTGCCTGAGCCC | 9051 |
rs182512082 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015748 | GGTGAAGGAGGAGGG[A/C]GCGGGCTGGGGGAAG | 9051 |
rs182625581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025085 | TTTAATTTGCAGAGA[G/T]CTTTGTCTTCCAGAA | 9051 |
rs182733577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029372 | GTGGTCCTCTGTGGG[C/T]GGAGGTTGCTTGTGG | 9051 |
rs182793342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035718 | AAGAGGCAGGGCCCA[C/G]CATGGAGAAACCCCA | 9051 |
rs182837178 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993369 | CCCGTCACCAGCATG[A/G]CCCTCCATCCGGGGC | 9051 |
rs182848045 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023780 | GAGGCGGGGCTGGAG[C/G]GTGGTGTGCGTAAGG | 9051 |
rs182926356 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006002 | TTTAGATTATACCTA[G/T]GAGTGGAATTGCTGG | 9051 |
rs182933082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002969 | TCAAGGTGGGAGGTA[C/T]GGCATGGGCAAAGGT | 9051 |
rs183066761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998487 | TTTTACTCAGGTCCT[A/G]TGAACTCTAATTTCA | 9051 |
rs183090210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020509 | GCAGCTGTTCCTTTC[A/G]GTGTAGGCCAAGCAT | 9051 |
rs183219503 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003791 | TGCAGGATGTCAGGG[G/T]CGTCATCACTTAAGA | 9051 |
rs183334369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014536 | CGAAAGGGGGTTAGC[C/T]TCCTGCCCCCACTTT | 9051 |
rs183439834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010340 | GGGGATCATGCGTGA[A/G]AGCCCCACCAGGCAC | 9051 |
rs183441330 | snp | A/G | 0.00173129 | 0.0293709 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77030494 | CCTGAGGCTGCCTGC[A/G]CTTTCAGAGCGGGTA | 9051 |
rs183602344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034340 | CACGTGTGTCTGCCC[A/G]CCTGTGTTGGTGTCA | 9051 |
rs183842796 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995257 | CCCTGCCCTGGGTCC[C/T]AGACTGTGTCCTCCA | 9051 |
rs183867383 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036624 | GATGAGGCCAGGGCT[C/T]GGGGAGGCAGGGAAG | 9051 |
rs183875014 | snp | A/C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016251 | CCCAGTTCTCAGGGC[A/C/G]GGGGGGTCTGTGGCA | 9051 |
rs184052999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997753 | TAAGAAAATCAGACA[A/C]GGTGGCTAGAACAAT | 9051 |
rs184097005 | snp | C/T | 0.0166325 | 0.0896639 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037593 | GGCTCAGCAGGGCTG[C/T]AATGGGGAGAGCAGG | 9051 |
rs184207978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018882 | CCTGCAGCACTGGCT[C/T]AGCATGGGCTTCAAG | 9051 |
rs184256158 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011806 | GACTGTAGTGATGGG[C/T]GCTCCTCACCTGTCA | 9051 |
rs184279306 | snp | C/T | 0.0116906 | 0.0755554 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77025624 | GGCAGGTGCAGGGGG[C/T]GGGGGAGCTGCTCCC | 9051 |
rs184286558 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006853 | TTACTGTAGCTTTGT[A/G]GTAAGCTTTGAAATC | 9051 |
rs184404010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021975 | GTTTGGGAAACAAAG[A/G]AAAACCAAGGCAAGG | 9051 |
rs184420207 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001368 | CAGGAGCTTTTTCAC[A/G]CAGGAAGGAGGGACC | 9051 |
rs184445497 | snp | A/G | 0.0159887 | 0.08797 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031132 | GCCCAGCCTGGCCGG[A/G]CCCTGCAGCCGCCTC | 9051 |
rs184466494 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026803 | GAGCTGGGACGTGCC[C/T]GCAGAGCCTGCAGAG | 9051 |
rs184554198 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007653 | AAGCTGGAGTGCAGT[A/G]GCACAATCTCAGCTC | 9051 |
rs184566526 | snp | A/G | 0.00699525 | 0.0587256 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008089 | AGCTGGGGGTGGAGG[A/G]CGGGAGATCAGCACA | 9051 |
rs184690364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025972 | CTTGAGTCCAAGGAT[C/T]AGGGCTGATTGTCCT | 9051 |
rs184762700 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031790 | CTGTGGATGGATGCA[A/G]CCCAGCACACGGCTC | 9051 |
rs185038806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022505 | CAACATGCGATGGAG[A/G]CACAGTAGAGGTGCT | 9051 |
rs185059685 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013361 | AGTTTCCTCCCTTGC[A/C]ATGGGGTACCCACAC | 9051 |
rs185140987 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017166 | GAGAGCTCAGGGGGT[A/T]GTGGCGGGGATCCTG | 9051 |
rs185243245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036887 | ATGGGAGGCCCGGTC[C/T]GTTGGGTTACCCCCA | 9051 |
rs185254155 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996372 | CTCAGCACTTTTCCA[C/G]CTGTCCTTCAACTAC | 9051 |
rs185263091 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030909 | CTCAGGACTCCCGTC[C/T]GAGGTCCCTCTCACT | 9051 |
rs185298667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017688 | GTTCAAGGCCAGGCC[A/C]GCCACTTTCCAGCTG | 9051 |
rs185302675 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037293 | GCCCCGAGAGGGAGC[C/T]TGTCGTCTCCCAGGG | 9051 |
rs185306283 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996991 | CAGGACCCCTTGACT[A/G]TTTTATCACTGAGAC | 9051 |
rs185334795 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010772 | CCTGCCTCACCCTCC[A/G]AGTAGCGGGGATTAC | 9051 |
rs185380772 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76999644 | CTACTAGGTGGTCCA[C/T]GCTGGACCCCTGAGC | 9051 |
rs185489191 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021572 | CAGTCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 9051 |
rs186039929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002198 | CTAAGGCACGGCAGG[C/T]CTAGGCCCAGACGAG | 9051 |
rs186070824 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033111 | GTGGAGACAAGATAG[G/T]CTCAGTTCAGCCTAT | 9051 |
rs186086597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008475 | AGTGCAGTGGCACCG[A/T]GTCGGCTCACTGCAA | 9051 |
rs186088669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027680 | CTCTGTGGCCTTCCA[C/T]TGTGAGGGTCACTGT | 9051 |
rs186109649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013574 | GTCCCTGACCACTCC[A/G]TTCCCTACAGCCTTC | 9051 |
rs186150576 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033756 | ATTCCAGGGCCTCAG[A/G]AGCCCCTGGAACTTC | 9051 |
rs186197236 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003557 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCGC | 9051 |
rs186215971 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009040 | GCCCCTCAACTCTCT[C/G]AGCCTTGGTTCCTTG | 9051 |
rs186237762 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023178 | GAGAAAATTTAGATT[A/T]TGAGCCTGGGGACAA | 9051 |
rs186359802 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029091 | GCCCATGCTCCTGAT[G/T]CTGTGGCCCCTAGGC | 9051 |
rs186738692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019779 | CTGGGCACAGAGGAG[A/G]GCTCAGGACATGGTG | 9051 |
rs186781354 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009873 | GACATCCCTGGCAGG[C/T]GTAGGTGGTGTGGGA | 9051 |
rs186871734 | snp | A/G | 0.0045539 | 0.0474996 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032518 | CTTCAGGGCAGAGAA[A/G]CCCTAGCAGGGGTTG | 9051 |
rs186945348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997912 | GGCACTGTCATTAAA[C/G]CCTTCAGCCTGCCAG | 9051 |
rs187002966 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002548 | TTTCCACATGCTCGG[G/T]GCATATTTTGTGGTA | 9051 |
rs187039996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998669 | CTGATTGCAAGGAAG[A/G]AGACAGAAACAGTCT | 9051 |
rs187063186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020710 | AGGGCCCATTTATGC[A/G]CCACCTCCTCCAGGA | 9051 |
rs187096653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013012 | CCATGGAGCTCAGCC[C/T]TTCCTACCTCAGGTT | 9051 |
rs187185878 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993546 | GTGGGAAAGGTGCCT[C/G]CAGGGAGAGGGAAGA | 9051 |
rs187207524 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015910 | CTGGGCGGGATCCTG[A/G]AGCCTGCAGCCTCTG | 9051 |
rs187211142 | snp | A/G | 0.000232627 | 0.0107824 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035861 | GTCTACACAGCCATC[A/G]CAGTGCAGGAGATAC | 9051 |
rs187247495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022952 | GGACAAATGGGAGTT[C/G]AAGGTGAGCACAGAC | 9051 |
rs187435273 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012959 | TAGGCACCAGGTGCC[A/G]GGATCCAGTGGGGAA | 9051 |
rs187507143 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007155 | AAGAAGGTCCATCTA[C/T]GACATCTCGGCTTCC | 9051 |
rs187712861 | snp | A/G | 0.00435818 | 0.0464768 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029621 | GGCGGAGGCCTGGGC[A/G]GTACTCCCCACACAC | 9051 |
rs187746870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998977 | AGCCTCAGAGTGGGA[C/T]CTGTCAGTGAGACAA | 9051 |
rs187760158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010421 | GACCTCCTGGGAAGG[C/T]CCTGCCCTTTGCTGT | 9051 |
rs187765023 | snp | C/T | 7.47957e-05 | 0.00611492 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030604 | GCCCACGTGGAGCCT[C/T]GTTTTCCCCAGCTGG | 9051 |
rs187870253 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010931 | GATTTCAGTTGTGAG[C/T]CACCACGTCCAGCCC | 9051 |
rs188001980 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023805 | GTAAGGGCTGGGTTG[C/G]GGGTGCGGGGACCAC | 9051 |
rs188036356 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021501 | CTGGCCAACATGGTG[A/C]AACCCCGTCTCTATC | 9051 |
rs188176145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030926 | AGGTCCCTCTCACTA[C/T]CCTTCTGCCTCGGTG | 9051 |
rs188278080 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004579 | AGAACAGTGGCCAGG[C/T]GTGGTGGCTCACACC | 9051 |
rs188458466 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022141 | ATTTTTAAAATTTTT[G/T]TCATGGTCTCTCTTC | 9051 |
rs188467602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001747 | CCTGGTCGGCAACCC[A/G]TTGTGAAAAGTGGGG | 9051 |
rs188472490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012060 | CTTCCCTCCCTATCA[C/T]CTCCTCCCAAATACT | 9051 |
rs188478499 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031650 | GCCTGGTGCTTGCAG[A/G]AGCCGAGGCGCAGTC | 9051 |
rs188548246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035351 | CTCCTGCCTGAGGGG[C/T]ACCTCATAAATGACA | 9051 |
rs188597511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017915 | CAGGCCCGGCACCCC[C/T]GGCCCTGTCAGCTGG | 9051 |
rs188609490 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997479 | AAAGATGTGCCAGGC[A/G]CTGTTCTCAAGATGT | 9051 |
rs188633961 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037322 | GGAATAAAGGAGTGC[A/G]TTCTGTTCTCCTTGG | 9051 |
rs188673763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006234 | ATGATGTTGAGCATC[C/T]TTTCATGTGTTTATT | 9051 |
rs188791228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014985 | GTGCCCGCTCCCCAC[A/C]TGGCACCCCTAATCC | 9051 |
rs188931087 | snp | A/G | 0.00216209 | 0.0328081 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77025338 | GTCCCCTACCCTGGG[A/G]CAATGGGATCTTTTG | 9051 |
rs189351725 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002391 | GTAGGATTCTCTCCA[C/T]CCCCCATCTAATTTT | 9051 |
rs189368761 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036640 | GGGGAGGCAGGGAAG[C/T]CAGGCCAGGAGAGTG | 9051 |
rs189377003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008320 | GGTCAGAGCAGGAGC[C/T]GCTCTGAAGCTGCAG | 9051 |
rs189414712 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027030 | CAAGGACATGTGCTT[A/T]CAGGATGGTGCACAC | 9051 |
rs189523620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013400 | CAGCTGCCTCTGGGG[A/T]CTCCATGGGGGGGTG | 9051 |
rs189527619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033360 | CCCCGGCCTGGCTGC[A/C]GTCAAGTGCCAAGGT | 9051 |
rs189528452 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012362 | ACCAGTCCACCCATC[C/T]ACCCACCCACCTATC | 9051 |
rs189640841 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022718 | TTGAAATTTCATCTG[A/G]GGCCAAGAAAGGGAG | 9051 |
rs189647591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77026136 | GGCTGTCCCGAGACA[C/G]AGTGACTGCATGGAA | 9051 |
rs189773500 | snp | C/T | 0.00240465 | 0.034591 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77032931 | GCCCTGGCATACAGC[C/T]GTCCTGCGGCATGAT | 9051 |
rs189869922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007785 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGGTT | 9051 |
rs190173070 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036974 | GCTGGGTGGGGGAAC[A/G]CCAGGCCCCTCCCTG | 9051 |
rs190185032 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996482 | GCTGTCCCGGGGTGC[C/T]GCCTCCAACCCCGAA | 9051 |
rs190215098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003718 | CCCAACCCTCACCCA[C/T]ACTTGCTAGGTGGCC | 9051 |
rs190219575 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023513 | AAAATAGAAGGTGGC[A/G]GCAAGGAAGGGAGAG | 9051 |
rs190309944 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016482 | CAGTGATGTCAACCT[A/G]GACATGGGGGTGGGC | 9051 |
rs190417422 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021843 | ACCCATCCCTCAAGG[C/G]CTGCCTGAAATGTCA | 9051 |
rs190429308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017199 | CCCGGGACCCACTCC[C/T]CAAGCCTGGGAATGT | 9051 |
rs190444505 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998327 | TACAGAACACGGGGC[A/G]GAGGAGGGGAGCCAG | 9051 |
rs190458949 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008896 | TGGCTGTGTTGGGCA[C/G]AGCAGGGCGATTTCC | 9051 |
rs190463341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028724 | CAAGGAAGGGGTGCC[A/G]TAGACACCCCCAGGC | 9051 |
rs190623486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005623 | CTGAACAGAAATTGT[A/G]CCCATCAAACAATAA | 9051 |
rs190672871 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000987 | CTCCCCTTTTTTTAG[C/G]GTAACTCACTCCATC | 9051 |
rs190854302 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030280 | ATATATGAGGCTCCA[C/T]TCCAGCCCTCAGGCA | 9051 |
rs190862146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010051 | CAGTGCCTCCTCCAG[A/G]GCTTGGGGTCTGGGG | 9051 |
rs191094301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002949 | GTCAGGAGGACAAAC[A/G]GCACTCAAGGTGGGA | 9051 |
rs191126700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013098 | CAGCCACACTGGCTG[C/T]AGATGTCACTGCTGG | 9051 |
rs191252796 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993637 | AGGGAGCCCAGCTGT[A/G]AAAATTTCTGCCAAT | 9051 |
rs191260518 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029173 | CACAGACAGGAAGGC[C/T]GAGGCCCAGAGAGGG | 9051 |
rs191280635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036051 | TCACTCATCTTCGAG[C/T]ATCCTCTCCTCCTCA | 9051 |
rs191291154 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015935 | CCTCTGGGGACTTGA[A/C/G]CACGGCGGTCACAGC | 9051 |
rs191521329 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009442 | CTCATATCAGCCCTA[G/T]AAGGGCTTAGGAGTC | 9051 |
rs191658871 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007374 | GCACTCTGGAAAGCT[A/G]AGGCAGGTGGATTGC | 9051 |
rs191661373 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025822 | CTCTTAGTCCCAGAG[A/C]CCCATGGAAGGTCCT | 9051 |
rs191670863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020489 | AGTACTGTTGATGAG[A/G]CCATGCAGCTGTTCC | 9051 |
rs191849553 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998850 | CAGATGCACGCTGCT[A/G]TAGGAGTGAGGCAGG | 9051 |
rs191880351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021312 | ACTCAGCAAACATCC[A/G]TGGGGCAGTGGCAAT | 9051 |
rs191912799 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018637 | GAGGCTGGGCAGAAC[C/G]AGGGTAGGTCTGGAT | 9051 |
rs191933101 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021935 | TGGGGGTGCTGCATG[C/T]CCCCAGAAGCTGCAC | 9051 |
rs191948287 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030750 | GGGCCCTGGCCCTGT[G/T]GCTTGTCGCCTGGCC | 9051 |
rs191956210 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001195 | TGGGTAGATCTTTGA[C/T]TATAAAGGTTTTTCA | 9051 |
rs192034642 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022993 | AAGACTGTCCCAGGG[G/T]TGGGACAGAGGCTGA | 9051 |
rs192217206 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997735 | TCTTATCTCCCAGAG[A/G]GGTAAGAAAATCAGA | 9051 |
rs192240509 | snp | A/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018010 | AAGCCAGGTCTGGAG[A/T]CCCAAGAGCTTGCCC | 9051 |
rs192256066 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037536 | ATTCACACCTGGACA[A/G]AGGACACAGGGGTGC | 9051 |
rs192383615 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013614 | CCTCTCCCGTTGCAC[C/T]CAATAGTCTGCTCCA | 9051 |
rs192608119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025396 | GGGGACAGAAGATGA[A/G]GTGTTGGGGCTGGGG | 9051 |
rs192626203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006426 | TGTCTTTTCACTGTT[C/T]TGATATACAAAAGTT | 9051 |
rs192673278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015436 | TGATACCCTTGGTGC[A/C]GTGTGTGCCAGGTAG | 9051 |
rs192774024 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030946 | CTGCCTCGGTGTGGT[A/G]CAGCCTGAAGGGAGG | 9051 |
rs192817830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010761 | AAAGTGATTCTCCTG[C/T]CTCACCCTCCGAGTA | 9051 |
rs192912170 | snp | G/T | 0.00281945 | 0.0374403 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035582 | AAGGGGGTCAGGAGG[G/T]GACCCCCAAACACAC | 9051 |
rs192967258 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011399 | AGCCCAGGCATCTCT[A/G]GGACTCGGCCAGCTG | 9051 |
rs193095562 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021508 | ACATGGTGAAACCCC[A/G]TCTCTATCAACAATA | 9051 |
rs193136723 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995772 | CCCAGGCCCCCACCC[A/C/G]TTCTGGACTGGAACG | 9051 |
rs193251337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:76999569 | CAGGCGTGAGCCGCC[A/G]CGCCCAGCACTACAT | 9051 |
rs193290011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016498 | GACATGGGGGTGGGC[A/G]CCTGCCTCTGAGGCT | 9051 |
rs199551920 | snp | A/G | 2.07855e-05 | 0.00322371 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032253 | CAGGCCCACAGAGGG[A/G]CAGAGTGGGCATCGG | 9051 |
rs199557447 | snp | A/C | 5.86872e-05 | 0.00541665 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037210 | TTCGGACCTGCCCTG[A/C]CAGTGGAGCCAGCAG | 9051 |
rs199749243 | in-del | -/CC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027333 | CCAGTGGCCACTGTG[-/CC]TGCATGTGGCCTGTG | 9051 |
rs199800583 | snp | A/G | 1.65831e-05 | 0.00287945 | missense, utr-variant-5-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995595 | CCCCAGCTGCAGTTC[A/G]AAGATGCCTTTTGGG | 9051 |
rs199804922 | snp | C/T | 0.000101396 | 0.00711953 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77037107 | CCTGGAAGGGGAGGA[C/T]GGCTGGTGGACTGTG | 9051 |
rs199891584 | snp | C/G/T | 1.6834e-05 | 0.00290116 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032965 | GAGGTGAGGCCCCGA[C/G/T]AGACGGAGGGAGGGC | 9051 |
rs199952167 | in-del | -/A | 0.00589129 | 0.0539531 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018268 | GCTGCTGGGCAGGCC[-/A]TGGGGAGCGCAGGCA | 9051 |
rs199993948 | in-del | -/ATCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012459 | CCCATCCACCCATCC[-/ATCC]ACCCACCCATCTACC | 9051 |
rs200011707 | in-del | -/CTC/TC | | | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037329 | GGAGTGCGTTCTGTT[-/CTC/TC]CTCCTTGGTGTGCTG | 9051 |
rs200018722 | snp | A/C | 0.00163912 | 0.028581 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028548 | CACGCCCCTCCACAC[A/C]CCCAGTCCAAGAAGA | 9051 |
rs200086068 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027248 | TGTCCTGGCTGTTTT[G/T]CCTTCTCTATCAGAA | 9051 |
rs200188483 | snp | C/T | 0.000219829 | 0.0104817 | missense, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035931 | TCTACGATTATACAG[C/T]GCAGGTGAGGCCTCT | 9051 |
rs200214727 | in-del | -/AAAG | 0.00993419 | 0.0697739 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004889 | ACAAACAAAAAAAAC[-/AAAG]AAAGAAAAGAGAAGC | 9051 |
rs200256020 | snp | A/G | 0.000117872 | 0.00767607 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037025 | CTTCCAACGTCATGC[A/G]CTTTCAATCTCTTGG | 9051 |
rs200348711 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000480 | ATATATATATATACA[C/T]ACACACACACACACA | 9051 |
rs200363654 | snp | A/C/T | 0.00163879 | 0.0285815 | missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037146 | CGGGCAGCGTGGCTT[A/C/T]GTCCCTGGTTCCTAC | 9051 |
rs200459219 | snp | A/C | 0.00011787 | 0.00767601 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031167 | CTGCTCACCTCCCTC[A/C]CACTGCCCCCAGGCC | 9051 |
rs200475800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77028531 | CTGTGCAGCCCCCAA[C/G]TCACGCCCCTCCACA | 9051 |
rs200614315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035971 | ACCCACCTGTGCCAC[C/T]TCCCCTGCACCTGAG | 9051 |
rs200698786 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997700 | CTTTTGGCTTCGGGG[-/A]TAAGATAAGAGGTAA | 9051 |
rs200752088 | snp | A/G | 0.00574999 | 0.0533098 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031143 | CCGGGCCCTGCAGCC[A/G]CCTCCTCACTGCTCA | 9051 |
rs200771233 | snp | A/G | 0.00238095 | 0.034421 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037076 | ACCTGTCCGCGGGAG[A/G]CATCCTGGAGGTGAT | 9051 |
rs200778419 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020878 | TCCTGTGGGGGGGGG[C/G/T]GGTGTGTGTGTTGGC | 9051 |
rs200796501 | snp | A/G | 0.0010153 | 0.0225082 | intron-variant, synonymous-codon, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032905 | TCGGGAGGTCACCCC[A/G]CTGACCAGCAGCCCT | 9051 |
rs200876675 | snp | C/T | 0.000541712 | 0.0164488 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035494 | CACTCACCCTCTTTC[C/T]TCCCTGTTCCCAGGT | 9051 |
rs200998074 | snp | C/T | 0.00012228 | 0.00781826 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030567 | TGGGAGCAGGAGCAC[C/T]GGACCACCTGTGAGG | 9051 |
rs201013929 | in-del | -/AG | 0.0448719 | 0.142907 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037544 | CTGGACAGAGGACAC[-/AG]GGGTGCAGGAGGATG | 9051 |
rs201093185 | in-del | -/CACAGCTGT | 0.0126979 | 0.078662 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031582 | GGGAGGGGAGGTGGA[-/CACAGCTGT]CAGAGGTTGGCAGAA | 9051 |
rs201186216 | snp | A/G | 0.0008062 | 0.0200612 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035870 | GCCATCGCAGTGCAG[A/G]AGATACAGGGAAACC | 9051 |
rs201221498 | snp | A/G | 0.000272996 | 0.01168 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037005 | CAGGCCCTTCCCTGC[A/G]GGCCCTTCCAACGTC | 9051 |
rs201253322 | snp | C/T | 0.000938993 | 0.0216475 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037138 | GAGAGGAACGGGCAG[C/T]GTGGCTTCGTCCCTG | 9051 |
rs201466172 | snp | A/G | 0.000528691 | 0.0162501 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032418 | CGGCTTGCGGACAGC[A/G]CAGCCTCTAGGTGCA | 9051 |
rs201535027 | snp | C/T | 0.00679149 | 0.0578759 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037214 | GACCTGCCCTGCCAG[C/T]GGAGCCAGCAGTGCC | 9051 |
rs201572812 | snp | A/G | 0.000477694 | 0.0154473 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037133 | CTGTGGAGAGGAACG[A/G]GCAGCGTGGCTTCGT | 9051 |
rs201582038 | snp | C/T | 0.00460067 | 0.0477406 | synonymous-codon, nc-transcript-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77035518 | CCCAGGTTCTCTGGA[C/T]TGCTGCACGGAAGTC | 9051 |
rs201587396 | snp | C/T | 0.226484 | 0.248892 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000476 | ATATATATATATATA[C/T]ACACACACACACACA | 9051 |
rs201636286 | snp | A/C | 2.21334e-05 | 0.00332659 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032440 | CTAGGTGCATTGAGC[A/C]CCTGGGAAGGCCCGG | 9051 |
rs201638707 | snp | C/T | 1.86353e-05 | 0.00305243 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030601 | GTGGCCCACGTGGAG[C/T]CTCGTTTTCCCCAGC | 9051 |
rs201738448 | snp | A/C | 1.6646e-05 | 0.00288491 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025267 | CTCCTCCTGACCTGG[A/C]CCCATCTGTTTTGCA | 9051 |
rs201770311 | snp | C/T | 1.69781e-05 | 0.00291355 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032345 | CTGCAGCATAGACGC[C/T]GACATCGACAGTTTC | 9051 |
rs201788590 | in-del | -/TCCCTGCAGGCCCT | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036984 | GGAACGCCAGGCCCC[-/TCCCTGCAGGCCCT]TCCCTGCAGGCCCTT | 9051 |
rs201795289 | snp | A/G | 0.000102109 | 0.0071445 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031130 | GGGCCCAGCCTGGCC[A/G]GGCCCTGCAGCCGCC | 9051 |
rs201816551 | snp | C/T | 0.000488656 | 0.0156233 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037024 | CCTTCCAACGTCATG[C/T]GCTTTCAATCTCTTG | 9051 |
rs201833364 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77016976 | GTAATGTGTGTGGTC[-/A]GGGGAGCTGGGACTT | 9051 |
rs201872851 | snp | C/T | 0.008118 | 0.063191 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77018522 | AGGCAGGTGGCCAGA[C/T]GGAGATCAAGTAAGA | 9051 |
rs201889539 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009460 | GGGCTTAGGAGTCCA[C/T]GTATTCTCCCCAATT | 9051 |
rs202014477 | in-del | -/CATCCATG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012298 | ACCCACCCATCTACC[-/CATCCATG]CATCCACCCACTCAC | 9051 |
rs202205180 | snp | C/T | 0.000436271 | 0.014763 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037070 | AGCTGGACCTGTCCG[C/T]GGGAGACATCCTGGA | 9051 |
rs202234078 | snp | C/T | 9.87898e-05 | 0.00702746 | synonymous-codon, nc-transcript-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77035532 | ACTGCTGCACGGAAG[C/T]CCCAAGACCACTTCG | 9051 |
rs367556424 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77027306 | TTTGGCCCCAGACCT[C/T]GGCACAGGGGCCCAG | 9051 |
rs367566326 | in-del | -/CATC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012549 | ATCCATCCATCCATC[-/CATC]AAGTTGTACCTGAGT | 9051 |
rs367643394 | snp | A/G | 9.70751e-05 | 0.00696621 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035887 | GATACAGGGAAACCC[A/G]GCCTCACCAGCCCAG | 9051 |
rs367755998 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77008644 | CGCACTCCTGACCTC[A/C]GGTAATCCACCCGCC | 9051 |
rs367777204 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016230 | GGGAAGCCGCACAAG[A/G]TGGTTCCCAGTTCTC | 9051 |
rs367791620 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033536 | CTATAGCCAGCTTAG[A/G]GAGCCCTCGTAGCCA | 9051 |
rs367828460 | snp | A/G | 0.000117007 | 0.00764786 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035474 | CCCTGAGTGTGGGGC[A/G]GGGACACTCACCCTC | 9051 |
rs367859628 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026950 | GGCCCCGCAGGCAGA[A/G]CGCTGTGTTGTAGTG | 9051 |
rs367860544 | snp | A/C | 9.85367e-05 | 0.00701845 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018539 | GAGATCAAGTAAGAT[A/C]TCCCGGGCCCTGGGG | 9051 |
rs367861858 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999419 | GAGTAGCTGGGATTA[C/G]AGACGTGCGCCGCCA | 9051 |
rs367882218 | snp | A/G | 5.04443e-05 | 0.00502191 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037032 | CGTCATGCGCTTTCA[A/G]TCTCTTGGCCAGAAC | 9051 |
rs367975984 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031429 | GCAGCTCAGCCTTTG[C/T]CCCCAGAACCCCAAG | 9051 |
rs368099765 | snp | A/G | 0.304688 | 0.243945 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035766 | GGGGCCAGTGTCCCC[A/G]GAAGGGGAGGGGTCT | 9051 |
rs368114895 | snp | A/C | 0.000161987 | 0.00899818 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027908 | GCTCTACAAGAAGGC[A/C]ATGGAGGTGAGCGCC | 9051 |
rs368144245 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022402 | GAGCTTCCTGAGAGC[C/T]GAGTCAAAAAGGGCA | 9051 |
rs368153325 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001330 | CAGTCACTTTGGGAT[-/T]CCCCCATAGTCCTCT | 9051 |
rs368186167 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034489 | GGGCTGCCCCCCACA[G/T]GCCCCTGAGTCATGG | 9051 |
rs368186634 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007308 | GCCTCAGCTTGCCTG[C/G]ATAAAAATCAGACTT | 9051 |
rs368237156 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012101 | AACCGCCTTGTTTAC[G/T]GAGGGCTCTGGCCAT | 9051 |
rs368315332 | snp | A/G | 7.36187e-05 | 0.00606663 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030595 | AGGTGAGTGGCCCAC[A/G]TGGAGCCTCGTTTTC | 9051 |
rs368373680 | snp | C/T | 0.000145875 | 0.00853911 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035920 | GTACCGGGCGCTCTA[C/T]GATTATACAGCGCAG | 9051 |
rs368431498 | snp | G/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999104 | CCCTGCCCCCAGTTT[G/T]TCGTGGCTCCACTCC | 9051 |
rs368477308 | snp | A/G | 0.000182711 | 0.00955625 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995573 | CGGCAGACGCCTGAG[A/G]ATGATGCCCCAGCTG | 9051 |
rs368482922 | snp | A/G | 1.79897e-05 | 0.00299908 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035864 | TACACAGCCATCGCA[A/G]TGCAGGAGATACAGG | 9051 |
rs368503235 | snp | C/G | 1.72659e-05 | 0.00293814 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995525 | CCTGGCCCTCCATCA[C/G]GCCAGCCTGTGGCAG | 9051 |
rs368508569 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034332 | GGAGCTGGCACGTGT[A/G]TCTGCCCGCCTGTGT | 9051 |
rs368528834 | snp | C/T | 0.000101779 | 0.00713298 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032351 | CATAGACGCCGACAT[C/T]GACAGTTTCATCCAG | 9051 |
rs368568162 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011863 | ACAGCCATTCAGGCT[C/T]CTGGGAAGCCTTTCC | 9051 |
rs368603281 | snp | C/G | 5.66396e-05 | 0.00532133 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76995399 | TGAGCTTTTTCCTCC[C/G]CTCAGAAGCTCCTCT | 9051 |
rs368613198 | in-del | -/G | 0.000547495 | 0.0165363 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77007971 | CCTGAACAATTGCCC[-/G]ATTGACCTGGACCAG | 9051 |
rs368685017 | snp | A/G | 6.86118e-05 | 0.00585672 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032321 | GGAAGTGCGGCTGAC[A/G]CTGGAAGGCTGCAGC | 9051 |
rs368769763 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037578 | GCAGGGGCAAGAAGG[A/G]GCTCAGCAGGGCTGC | 9051 |
rs368787271 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998848 | TTCAGATGCACGCTG[C/T]TGTAGGAGTGAGGCA | 9051 |
rs368838637 | snp | C/T | 0.00014043 | 0.00837825 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035830 | CCTGACCCCCACCCC[C/T]GAGCGGAATGAGGGT | 9051 |
rs368903832 | snp | A/G | 0.000277559 | 0.0117772 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018105 | GCTGTGCTCAGTGTC[A/G]CCTGGTCGTGGCCCT | 9051 |
rs368938689 | snp | A/G | 4.47477e-05 | 0.00472989 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028612 | CGGAGCAGGCCTTCG[A/G]GCGCATTAGCGCCAA | 9051 |
rs368974160 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77024915 | CCATTTGGTACCTGC[C/T]GAGGAGAGAGGGCTG | 9051 |
rs369016766 | snp | C/T | 1.66452e-05 | 0.00288484 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025327 | AAGCAGCGTAAGTCC[C/T]CTACCCTGGGGCAAT | 9051 |
rs369033286 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035325 | CCACCAGGACTACTT[A/T]CTGGGGAGCCCTCCT | 9051 |
rs369049458 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996189 | CAGACCTTAGGGGTC[C/T]TTCAAGGAGGCAGCC | 9051 |
rs369113632 | snp | A/C/G | 0.000635642 | 0.0178169 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037132 | ACTGTGGAGAGGAAC[A/C/G]GGCAGCGTGGCTTCG | 9051 |
rs369123276 | snp | A/G | 8.36785e-05 | 0.00646779 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037179 | GGAGAAGCTTTGAGG[A/G]AGGGCCAGGAGCCCC | 9051 |
rs369205216 | snp | A/G | 0.000103525 | 0.00719387 | synonymous-codon, nc-transcript-variant, missense | PSTPIP1 | GRCh38.p7 | 15:77035547 | TCCCAAGACCACTTC[A/G]TTGGCAGCTTCTGCT | 9051 |
rs369232421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014301 | CTCACCTATGCGCAC[A/G]ATTTCACTTGCTTCT | 9051 |
rs369291950 | snp | C/T | 0.000148998 | 0.00862999 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030631 | CTGGGAAGTGTGAGA[C/T]GCCCATCCCTACTCC | 9051 |
rs369296575 | snp | C/T | | | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024375 | TCCCCAGGTGTCTAC[C/T]GAGAGGAGAAGCCCC | 9051 |
rs369320360 | snp | A/G | 0.000110932 | 0.00744674 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77018553 | TCTCCCGGGCCCTGG[A/G]GCTCACTCCTCTCCT | 9051 |
rs369324680 | snp | C/T | 5.95717e-05 | 0.00545732 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035462 | CTCCTGGTGGGTCCC[C/T]GAGTGTGGGGCGGGG | 9051 |
rs369333365 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034634 | ATGCCTCCTCCCCTG[C/T]ACCTGAGCCCTCCCT | 9051 |
rs369498554 | snp | C/T | 0.000303493 | 0.0123148 | missense, nc-transcript-variant, intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035802 | TCACCCTGCTCTTAG[C/T]GTCCACAGAGACCCT | 9051 |
rs369508601 | snp | A/C/T | 4.99374e-05 | 0.00499666 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025268 | TCCTCCTGACCTGGA[A/C/T]CCATCTGTTTTGCAG | 9051 |
rs369568537 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030045 | CCTTCCCCTGGGAAG[A/G]CCTCTCCCTTCTGCT | 9051 |
rs369584394 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029785 | GTTCAGTCCTCACAG[C/G]TGCCCTCCGAGGTGG | 9051 |
rs369809954 | snp | C/T | 9.34187e-05 | 0.00683378 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032417 | CCGGCTTGCGGACAG[C/T]GCAGCCTCTAGGTGC | 9051 |
rs369835681 | snp | A/G | 0.000477374 | 0.0154421 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77035932 | CTACGATTATACAGC[A/G]CAGGTGAGGCCTCTA | 9051 |
rs369892385 | snp | C/T | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036247 | CACACACGTGGAGCA[C/T]ATGTACCTATGCCGT | 9051 |
rs369895864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023135 | CTGAGACCATGAACC[A/G]GGGTGGCCCACAGGT | 9051 |
rs369905474 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76996894 | GATGTGAGTCACCAC[C/T]TAGCTGCCCTGCCTT | 9051 |
rs369943879 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77009768 | TTGTGACTCATGCAG[A/G]CTGTGTGGAACTGGC | 9051 |
rs369985315 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023204 | GACAATGAGGAGGAG[-/A]GCCAGGCATTGCCCC | 9051 |
rs370003508 | snp | C/T | 3.90739e-05 | 0.00441989 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77028568 | GTCCAAGAAGACATA[C/T]GAGCAGAAGTGCCGG | 9051 |
rs370077811 | snp | A/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003434 | CGAGGCGGGTGGATC[A/T]TCTGAGGTCAGGGGT | 9051 |
rs370127747 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033868 | AAGCAGTGACCCCAG[A/G]AGGCAGCACACCCGC | 9051 |
rs370178664 | snp | A/G | 2.34877e-05 | 0.00342685 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030470 | GGAGGAGCTCGTGTC[A/G]GGGCCCTCCCTGAGG | 9051 |
rs370184738 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011285 | CAGTGCCTGTGTTGT[C/T]CCTTCAGTGGGACCC | 9051 |
rs370227630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998342 | GGAGGAGGGGAGCCA[G/T]CCCTGCTGTTTCTGG | 9051 |
rs370227919 | in-del | -/GA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034053 | AGAGAGAGAGAGAGA[-/GA]TGTCCTGCAGGGCCG | 9051 |
rs370302620 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77000122 | CTAGAAACCCCTGTG[A/C]CACACTGGGAGGAGC | 9051 |
rs370307155 | snp | A/C/G | 5.00482e-05 | 0.0050022 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031290 | TGAGGTGGGGGCTGA[A/C/G]GGCCTTGGTGTGGGG | 9051 |
rs370404621 | snp | A/G | 8.75971e-05 | 0.00661747 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035843 | CCCGAGCGGAATGAG[A/G]GTGTCTACACAGCCA | 9051 |
rs370427607 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010775 | GCCTCACCCTCCGAG[C/T]AGCGGGGATTACATG | 9051 |
rs370436334 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77026927 | GCATTCTTTCTCCAA[A/G]TGGCCAGGGCCCCGC | 9051 |
rs370462764 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018024 | GTCCCAAGAGCTTGC[C/T]CTGAGCAGGGGAGAT | 9051 |
rs370493795 | in-del | -/CTTGTGG | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037798 | AAGACAGGCTTGTGG[-/CTTGTGG]GTGCAAGTGGGGCCT | 9051 |
rs370601019 | snp | C/T | | | intron-variant, missense, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032943 | AGCCGTCCTGCGGCA[C/T]GATAAAGAGGTGAGG | 9051 |
rs370723493 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012159 | TCCATCCATCCATCC[A/G]CCCACCCACCCACCC | 9051 |
rs370740664 | snp | C/T | 1.78583e-05 | 0.00298811 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035860 | TGTCTACACAGCCAT[C/T]GCAGTGCAGGAGATA | 9051 |
rs370745407 | snp | A/G | 0.000297959 | 0.0122021 | PSTPIP1 | 15 | allele_origin=G(germline)/A(germline) | 15:77025614 | AAGAAGGTGAGGCAG[A/G]TGCAGGGGGCGGGGG | 9051 |
rs370752949 | snp | C/T | 1.68912e-05 | 0.00290608 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037010 | CCTTCCCTGCAGGCC[C/T]TTCCAACGTCATGCG | 9051 |
rs370756727 | snp | A/G/T | 0.000118275 | 0.00768933 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77032274 | TGGGCATCGGGCTGC[A/G/T]GCCTCTGCTCTTTCC | 9051 |
rs370766237 | in-del | -/AGAA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003668 | CTCAAAAAAAAAAAA[-/AGAA]GAAGAAGGAAGCGGG | 9051 |
rs370782742 | snp | C/T | 0.00099326 | 0.022263 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77029567 | CAAGGACTCGGCCAC[C/T]GAGGCAGGTATGTGG | 9051 |
rs370802825 | snp | C/G/T | 0.000243923 | 0.0110413 | missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018499 | GGAGCTGGTGCAGAT[C/G/T]GCACGGAAGGCAGGT | 9051 |
rs370886691 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012325 | CACCCACTCACCCAT[C/T]CCTCCATTTGTCCAC | 9051 |
rs370900344 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036854 | TTGGGGGAGAACTAT[C/G]ATGACAAACTGAGGG | 9051 |
rs370915799 | snp | C/G | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036216 | CAGGCCTGTGTCTGC[C/G]CGGGCCTGTACACAG | 9051 |
rs370965231 | snp | A/C/T | 0.000263634 | 0.0114783 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030526 | ACAGGCAGAGCATTG[A/C/T]GCAGCTGGAGAAGGT | 9051 |
rs370991369 | snp | C/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018412 | TGGGCCTCCCCCAGA[C/G]GTGGCAAGTCACTGA | 9051 |
rs371065077 | snp | C/G/T | 2.73319e-05 | 0.00369667 | missense, nc-transcript-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77025546 | TGGCCCTGACCCTGC[C/G/T]TGAGGAGCTGCGGAG | 9051 |
rs371102834 | in-del | -/CCT | | | utr-variant-3-prime, nc-transcript-variant, cds-indel | PSTPIP1 | GRCh38.p7 | 15:77037332 | AGTGCGTTCTGTTCT[-/CCT]TGGTGTGCTGGGGTC | 9051 |
rs371118536 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021774 | CCTGACTCTCCTTTC[C/T]AGCCTCTGGGCCTTT | 9051 |
rs371380285 | snp | C/T | 0.000303954 | 0.0123242 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:76995661 | GGGGGCAGAGCTAGG[C/T]TGAAATCTCCATGCA | 9051 |
rs371414090 | snp | A/G | 0.00010451 | 0.00722799 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77027826 | GAGGCCGCGGCCCTC[A/G]GCTCAGAACCTCGTG | 9051 |
rs371497170 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022833 | GCCTGCAGCCCAGGG[G/T]ACAGGAAGAGGGGCC | 9051 |
rs371548078 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022146 | TAAAATTTTTTTCAT[C/G]GTCTCTCTTCCTCTG | 9051 |
rs371568191 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034400 | TCCACCCTGCGCATG[C/T]GTGTGCACTCCTGGG | 9051 |
rs371644004 | snp | C/T | 4.72445e-05 | 0.00486004 | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995496 | CTGCCAGGACTGGGA[C/T]GCTGCTGCTGGCGCC | 9051 |
rs371698549 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77033759 | CCAGGGCCTCAGGAG[A/C]CCCTGGAACTTCCTA | 9051 |
rs371713485 | snp | A/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993562 | CAGGGAGAGGGAAGA[A/G]GCCTGGCTGGAGCAG | 9051 |
rs371715620 | snp | A/G | 1.83051e-05 | 0.00302527 | synonymous-codon, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032411 | TGAGGTCCGGCTTGC[A/G]GACAGCGCAGCCTCT | 9051 |
rs371781444 | snp | A/G | 6.71103e-05 | 0.00579229 | missense, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035910 | CAGCCCAGGAGTACC[A/G]GGCGCTCTACGATTA | 9051 |
rs371808472 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77030171 | CACCCCTCCTCCAGC[A/G]CCCTCTCAGCTGCCT | 9051 |
rs371810097 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013929 | GGAAGGTGTGTAGGG[C/T]GAGAGGGGAGGTGAT | 9051 |
rs371836861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76999428 | GGATTACAGACGTGC[A/G]CCGCCACGTCTGTCT | 9051 |
rs372008774 | snp | A/G | 0.000165961 | 0.00910786 | intron-variant, splice-donor-variant | PSTPIP1 | GRCh38.p7 | 15:77008066 | CTGAGGATGGTTCAG[A/G]CAAGCAGAGCTGGGG | 9051 |
rs372009472 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035767 | GGGCCAGTGTCCCCA[A/G]AAGGGGAGGGGTCTA | 9051 |
rs372035242 | in-del | -/TCCACCCA | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77012280 | CCACTCATCCACCCA[-/TCCACCCA]CCCATCTACCCATCC | 9051 |
rs372064325 | snp | A/G/T | 3.32919e-05 | 0.00407983 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025235 | CAGCCTGGACTGTAG[A/G/T]TTCCCGCTGTGCTCT | 9051 |
rs372074951 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77016063 | GAAGGGTTCCCTTGG[C/T]GTCAGGGCTGGGTGT | 9051 |
rs372097351 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77002545 | CCTTTTCCACATGCT[C/T]GGTGCATATTTTGTG | 9051 |
rs372261106 | snp | A/G | 0.000122927 | 0.00783891 | missense, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035921 | TACCGGGCGCTCTAC[A/G]ATTATACAGCGCAGG | 9051 |
rs372335370 | snp | C/T | 0.000332565 | 0.0128908 | PSTPIP1 | 15 | allele_origin=T(germline)/C(germline) | 15:77032969 | TGAGGCCCCGACAGA[C/T]GGAGGGAGGGCCTAA | 9051 |
rs372352159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023359 | GTGCAAAGGCCCTGA[A/G]GCAAGATGGAGCCTG | 9051 |
rs372384486 | snp | A/G | 0.000159987 | 0.00894249 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037128 | GTGGACTGTGGAGAG[A/G]AACGGGCAGCGTGGC | 9051 |
rs372385493 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77025380 | CTGGTGGAGGGTTTG[C/G]GGGGACAGAAGATGA | 9051 |
rs372407300 | snp | C/T | 0.000317219 | 0.01259 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995558 | GAGTGAGCTTTGCCG[C/T]GGCAGACGCCTGAGG | 9051 |
rs372461120 | snp | A/G | 0.000173506 | 0.0093125 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77030544 | AGCTGGAGAAGGTCC[A/G]GGCTGAGTGGGAGCA | 9051 |
rs372468528 | snp | A/G | 3.51068e-05 | 0.00418953 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035831 | CTGACCCCCACCCCC[A/G]AGCGGAATGAGGGTG | 9051 |
rs372481689 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017856 | CTCTTCCCATCTGCT[A/C/G]TCTCATGCTGATGTG | 9051 |
rs372534330 | in-del | -/CTGCAGGCCCTTCC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037001 | CCTGCAGGCCCTTCC[-/CTGCAGGCCCTTCC]AACGTCATGCGCTTT | 9051 |
rs372585630 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017872 | TCTCATGCTGATGTG[C/T]GTCCTGTCCTGTGAG | 9051 |
rs372638683 | snp | G/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004158 | AATGTGGGCCTGGGG[G/T]ATGCCACACAGATGG | 9051 |
rs372733304 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013426 | GGGTGGTGGGGCACA[A/G]GCCGTGACTGTAAAG | 9051 |
rs372738066 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77010414 | TTCCTATGACCTCCT[A/G]GGAAGGTCCTGCCCT | 9051 |
rs372789100 | snp | C/T | 4.28587e-05 | 0.00462898 | utr-variant-3-prime, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77037193 | GAAGGGCCAGGAGCC[C/T]CTTCGGACCTGCCCT | 9051 |
rs372796597 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035106 | GCTAGGGCAAGCTAG[A/C]GCAGGGGCCTGGAGG | 9051 |
rs372906701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PSTPIP1 | GRCh38.p7 | 15:77024373 | CTTCCCCAGGTGTCT[A/G]CTGAGAGGAGAAGCC | 9051 |
rs372953175 | snp | A/G | 0.000157988 | 0.00888644 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018110 | GCTCAGTGTCGCCTG[A/G]TCGTGGCCCTCATGT | 9051 |
rs372955697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036013 | CCATCCAGTGCCTTG[C/T]GTCCTCATCTCTCCT | 9051 |
rs372977437 | in-del | A/TC | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77007561 | TTGCAGTGAGCTGTA[A/TC]TCATGCCACTGCACT | 9051 |
rs372983486 | snp | A/G | 0.00151783 | 0.0275066 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029505 | GGGCAGGGGCTTAGC[A/G]CTGCTTCCCCTCTGT | 9051 |
rs372999755 | snp | C/T | 0.0090467 | 0.0666447 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036997 | CCTCCCTGCAGGCCC[C/T]TCCCTGCAGGCCCTT | 9051 |
rs373013073 | snp | A/G | | | utr-variant-5-prime, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:76995467 | CCGGCCGGGAAGGGG[A/G]GCCTGGGCCAGCCCT | 9051 |
rs373047005 | snp | C/T | 0.000202602 | 0.0100628 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77037017 | TGCAGGCCCTTCCAA[C/T]GTCATGCGCTTTCAA | 9051 |
rs373085195 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037357 | CTGGGGTCCCGTTCT[-/CT]TTTTCTCCTGCTCCA | 9051 |
rs373179590 | snp | A/G | 0.000202874 | 0.0100696 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031154 | AGCCGCCTCCTCACT[A/G]CTCACCTCCCTCCCA | 9051 |
rs373447022 | in-del | -/GGCTTGT | 0.0209421 | 0.100162 | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037789 | GAGCCCAGGAAGACA[-/GGCTTGT]GGCTTGTGGGTGCAA | 9051 |
rs373477497 | snp | A/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031455 | CCAAGACAGGAGCTC[A/G]GTACCACACAGGGCC | 9051 |
rs373483342 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77017053 | AAGACAGACTAGGTG[C/T]GGAATGTCAGGCCTG | 9051 |
rs373511603 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77003710 | AAGCCTCACCCAACC[C/T]TCACCCACACTTGCT | 9051 |
rs373516507 | snp | C/T | 0.000240544 | 0.0109642 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018177 | AGCCCACACGGGCTA[C/T]GAGGTGCTGCTGCAG | 9051 |
rs373587153 | snp | C/T | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998611 | ATGGATAAATGCTGA[C/T]GGACCTGGACTACGA | 9051 |
rs373692809 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019469 | CCCCAAAGACACCAG[C/G]CACCCTGGCGGCTCC | 9051 |
rs373751128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77023230 | GCCCCTGTCCTCAAG[A/G]GCTCATGGTTCAGCT | 9051 |
rs373839045 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77034210 | GAGGTGTGGGGGCAC[A/G]CAGCACAATGGCTCA | 9051 |
rs373872744 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77011839 | GCCCCCCACCCTCTT[C/T]CCATACCTACAGCCA | 9051 |
rs374042149 | in-del | -/CTATGCCGTCC | | | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77036254 | GTGGAGCACATGTAC[-/CTATGCCGTCC]ACACAGGCTGGGCGC | 9051 |
rs374045846 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76997884 | GTCTGGGCCTTCCCC[A/C/G]ACCCCAGCCCAAGGC | 9051 |
rs374055726 | snp | A/G | 8.33451e-05 | 0.00645489 | synonymous-codon, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77031230 | TCTCCGCAACGCCCT[A/G]TGGGTGCACAGCAAC | 9051 |
rs374056644 | snp | A/G | | | intron-variant, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76998322 | ACCCATACAGAACAC[A/G]GGGCGGAGGAGGGGA | 9051 |
rs374114250 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77014124 | GTTAACAGCCAAGAT[C/T]GTGGCTTGGGATATC | 9051 |
rs374131649 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013781 | AGCAGGTAGGAACTC[A/G]GACCAAAACCCAGGT | 9051 |
rs374204996 | snp | A/C/G/T | 0.000281123 | 0.011853 | intron-variant, missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032939 | ATACAGCCGTCCTGC[A/C/G/T]GCATGATAAAGAGGT | 9051 |
rs374212404 | snp | C/T | 8.71194e-05 | 0.0065994 | missense, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77027897 | AGCAAGCTGTCGCTC[C/T]ACAAGAAGGCCATGG | 9051 |
rs374264816 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77022278 | CTCAGCACAGGGAGC[C/T]GAGAGGGCTACTCCT | 9051 |
rs374319691 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77013339 | ATGGGGAAAAGAGAA[C/G]AGGGTCAGTTTCCTC | 9051 |
rs374322830 | snp | A/G | | | downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77037556 | CACAGGGGTGCAGGA[A/G]GATGTGGCAGGGGCA | 9051 |
rs374365958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77019314 | GGCAGACAGACCACC[A/G]GCCTCCAACTTCTTG | 9051 |
rs374371227 | snp | C/G | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77036471 | AGGGTGAGGATGAAC[C/G]AAGGCAGCCACAGGG | 9051 |
rs374381141 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77001457 | TGCACTGACTTTGTG[A/G]AAGGCCTTGCAGCCC | 9051 |
rs374459144 | snp | C/G | | | upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:76993283 | GAGGGGAGGAGGAAG[C/G]CCTCTCTAGTAGAGA | 9051 |
rs374490916 | snp | C/T | 0.000118575 | 0.00769892 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035473 | TCCCTGAGTGTGGGG[C/T]GGGGACACTCACCCT | 9051 |
rs374537305 | snp | A/G | 9.66044e-05 | 0.00694931 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77029609 | CCGTCCGACCAGGGC[A/G]GAGGCCTGGGCGGTA | 9051 |
rs374569576 | snp | A/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77021718 | TGCAGGGGGCTTACC[A/C]ACATTGCTGACATCA | 9051 |
rs374569732 | snp | C/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005469 | TGACCTCATTTGACT[C/T]ACCTGAGTGAGCAGA | 9051 |
rs374629699 | in-del | -/T | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77006146 | TTTCTGTTTTTTTTT[-/T]AAATCATAGCCACCT | 9051 |
rs374639723 | in-del | -/C | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77004454 | AACAGGAACGGGAAA[-/C]CAGCCACACTGGGGA | 9051 |
rs374682350 | snp | C/T | 1.77436e-05 | 0.0029785 | missense, nc-transcript-variant, utr-variant-3-prime | PSTPIP1 | GRCh38.p7 | 15:77035856 | AGGGTGTCTACACAG[C/T]CATCGCAGTGCAGGA | 9051 |
rs374739752 | in-del | -/GG | | | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77020879 | CCTGTGGGGGGGGGG[-/GG]TGTGTGTGTTGGCCC | 9051 |
rs374768418 | snp | A/C/T | 0.5 | 0 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77035765 | AGGGGCCAGTGTCCC[A/C/T]AGAAGGGGAGGGGTC | 9051 |
rs374876117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77015511 | ATTCGGATGACAGAG[G/T]TTGGACAGGATGAGG | 9051 |
rs374959699 | snp | A/G | 1.69738e-05 | 0.00291317 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77031139 | CTGGCCGGGCCCTGC[A/G]GCCGCCTCCTCACTG | 9051 |
rs375057169 | snp | A/C | 0.00115733 | 0.0240276 | intron-variant, downstream-variant-500B | PSTPIP1 | GRCh38.p7 | 15:77035987 | TCCCCTGCACCTGAG[A/C]GCTCCCTCTCCCATC | 9051 |
rs375063664 | snp | C/T | 0.000123122 | 0.00784513 | missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | PSTPIP1 | GRCh38.p7 | 15:77018503 | CTGGTGCAGATCGCA[C/T]GGAAGGCAGGTGGCC | 9051 |
rs375139167 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PSTPIP1 | GRCh38.p7 | 15:77005655 | TCCCCACCCCTTCAC[C/G]GCATACCTTGTTCTA | 9051 |
rs375155007 | snp | C/T | 1.73045e-05 | 0.00294142 | missense, intron-variant, nc-transcript-variant | PSTPIP1 | GRCh38.p7 | 15:77032313 | CTCTACGAGGAAGTG[C/T]GGCTGACGCTGGAAG | 9051 |