| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs137952652 | snp | A/C | 0.286825 | 0.247273 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210398 | GTTCTGGAAGTCATG[A/C]TGTGGGCTGTGTCTG | 100287144 |
| rs139813323 | snp | C/T | 8.97304e-05 | 0.00669755 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210939 | TACGTGAACGCTTCC[C/T]TGCAGTGCCTGACAT | 100287144 |
| rs142481985 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210496 | TTGGCTAATCGCGCA[C/T]CTGATGAGTGGGTGG | 100287144 |
| rs143756616 | snp | A/T | 0.191461 | 0.24305 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210259 | ACACACACGGTTTCC[A/T]AGGTAAAGATTTCTT | 100287144 |
| rs144060648 | snp | A/C | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212567 | ATTCAGTGTGTATTT[A/C]TGAATATGACCTACC | 100287144 |
| rs149415298 | snp | A/C | 0.411578 | 0.190768 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210229 | ACACACACAAACACA[A/C]TCACACACACACACA | 100287144 |
| rs149938208 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212548 | TGTGTTCATGATAGG[C/T]GACATTCAGTGTGTA | 100287144 |
| rs180979030 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209374 | CCCACTGAAACAAGG[A/G]CCAGTATTAAAAATG | 100287144 |
| rs181084641 | snp | C/T | 0.00304976 | 0.0389304 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210859 | CTCCCAGGGAGAAGC[C/T]TCCTCTGAGTAGCAG | 100287144 |
| rs181179919 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209334 | AGCGAGAATCCAGGA[G/T]ACACACGGCTTATTT | 100287144 |
| rs181304027 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212688 | ACGAGAAGGTGAAAT[G/T]TGGCTCATGTGGGAC | 100287144 |
| rs181412811 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208858 | TGCTTTCTCCCTGTG[G/T]AGCATCTTTCTAAGC | 100287144 |
| rs181632685 | snp | A/G | 0.00478085 | 0.0486577 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212418 | CAAGTTTCTGTCTGT[A/G]CAACAGGGACAACTG | 100287144 |
| rs181643214 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208800 | AAGCCACGGCATCTG[C/G]ATTGCTCATGCTTCT | 100287144 |
| rs181820493 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208908 | AGGAAACTTTACATC[A/C]GGCACAGGAAGCTTT | 100287144 |
| rs181833188 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209937 | AACACTTGTCTTGTT[C/G]TCCACTGGCAAGTAA | 100287144 |
| rs181950327 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209438 | AACGTCTCCGATGTT[G/T]CTTCTTGAGACAGGG | 100287144 |
| rs182083040 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209964 | GTAATTCAACACGGA[C/T]AGAGAATCAATAGGC | 100287144 |
| rs182169107 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210540 | GGTGTGGGTGAGTTA[C/T]AGAAGGGCTGATGCG | 100287144 |
| rs182339908 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209512 | GTTTGCTTTTGTCAA[A/C]CTTAGAACATTTTAT | 100287144 |
| rs182541833 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210069 | ACGCTGTGCTAAATA[C/T]TATACTTCATTGACT | 100287144 |
| rs182607432 | snp | C/G | 0.000697107 | 0.0186566 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212030 | AAGAGTCGAAGGTAC[C/G]GTGCCTCCCGACGTA | 100287144 |
| rs182819472 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209453 | TCTTCTTGAGACAGG[A/G]CCTCACTGCCGTCCG | 100287144 |
| rs183042461 | snp | C/T | 0.0010771 | 0.0231817 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210985 | CCAACTACATGCTGT[C/T]CCGGGAGCACTCTCA | 100287144 |
| rs183192822 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208994 | TCACACTCCTCTCAT[C/T]CCATCATACTCCTTA | 100287144 |
| rs183285001 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209024 | AAAATCATCCTAATT[C/T]CATGGGTCCTGAAGC | 100287144 |
| rs183368930 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209621 | TATTTTCATCACTTC[A/C]AGAAAAAAAAGGGTA | 100287144 |
| rs183631483 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209884 | CATATGATGCTTTAT[C/T]ATTTGGCAATCTAGC | 100287144 |
| rs183806930 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210103 | CTCAGGTCAGAAAGC[A/G]CACTTCCGAATTCTT | 100287144 |
| rs183818171 | snp | A/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210130 | TCTTGTCCTTCGGTC[A/G]CTGAGAGGATGATGG | 100287144 |
| rs183887405 | snp | A/G | 0.00140305 | 0.0264492 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211174 | CTGTGGATGCCATGA[A/G]AAAGGCATGCCTTCC | 100287144 |
| rs183981664 | snp | A/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212439 | GGGACAACTGGATAG[A/T]GATGGCTACATCTCA | 100287144 |
| rs183983725 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208826 | CTTCTGGGGATCATT[C/T]TCCTGAAAATCGTGG | 100287144 |
| rs184205409 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209197 | ATTCTGTCCCTCTTA[A/C]TTCAGGGAACGTGTC | 100287144 |
| rs184255491 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210378 | AGGAGTAATCTGATT[C/G]AGGTGTTCTGGAAGT | 100287144 |
| rs184637313 | snp | A/C/G | 0.00631449 | 0.0558334 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212190 | TCCCTACGAGGGAGG[A/C/G]CCAGGAGATCCAAAG | 100287144 |
| rs184639008 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209129 | TGTTGGGAAAGTCCC[A/T]AGAGCCAGGATCTTC | 100287144 |
| rs184665396 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209825 | TCCTACACAGTCTAC[A/T]TTGTGCACTGAGTAT | 100287144 |
| rs184768925 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208713 | GCTCCCCTCAAAAGC[G/T]GTTATGAGCATTAAA | 100287144 |
| rs184946946 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209336 | CGAGAATCCAGGAGA[A/C]ACACGGCTTATTTTG | 100287144 |
| rs184981556 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210095 | TGACTATTCTCAGGT[A/C]AGAAAGCACACTTCC | 100287144 |
| rs185462842 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210529 | TGTTCGCGGTTGGTG[G/T]GGGTGAGTTATAGAA | 100287144 |
| rs185609693 | snp | A/C | 0.000536241 | 0.0163656 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210958 | AGTGCCTGACATACA[A/C]ACCGCCACTTGCCAA | 100287144 |
| rs185624630 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212412 | GGAGCCCAAGTTTCT[A/G]TCTGTACAACAGGGA | 100287144 |
| rs185777226 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208881 | TTCTAAGCAGTGCTC[C/T]TTTCTTCCCACAGGA | 100287144 |
| rs186330055 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210056 | TAGGGAAGAAAATAC[A/G]CTGTGCTAAATATTA | 100287144 |
| rs186426447 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209391 | CAGTATTAAAAATGG[C/T]ATGCTATACTCTGTT | 100287144 |
| rs186545087 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209441 | GTCTCCGATGTTTCT[C/T]CTTGAGACAGGGCCT | 100287144 |
| rs186548755 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208921 | TCAGGCACAGGAAGC[C/T]TTCTGATGGAGCACA | 100287144 |
| rs186691912 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209538 | TTTATTTCGTCTCTA[G/T]GAAATGTTGATCCAT | 100287144 |
| rs186786338 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210566 | ATGCGGCCAGAGAGC[C/T]CGTCATTTGAAGACT | 100287144 |
| rs187120998 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209002 | CTCTCATTCCATCAT[A/C]CTCCTTAAAATCATC | 100287144 |
| rs187156447 | snp | A/T | 0.000470655 | 0.0153332 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211069 | CAAGGGCCCTCCACA[A/T]TCCTGGCCATGTCAT | 100287144 |
| rs187262693 | snp | C/G/T | 0.0312266 | 0.12106 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212076 | TCAAAATACAAGTGT[C/G/T]GGATGAAGAACCATC | 100287144 |
| rs187420227 | snp | C/T | 0.00575911 | 0.0533516 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211663 | ACAACGGACATTACT[C/T]CTCTTATGTCAAAGC | 100287144 |
| rs187455159 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209948 | TGTTGTCCACTGGCA[A/G]GTAATTCAACACGGA | 100287144 |
| rs187500889 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209031 | TCCTAATTTCATGGG[C/T]CCTGAAGCCAGGGCT | 100287144 |
| rs187608883 | snp | A/C | 0.00517822 | 0.0506191 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212192 | CCTACGAGGGAGGAC[A/C]AGGAGATCCAAAGGG | 100287144 |
| rs187857232 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209152 | GGATCTTCATTCCTG[C/G]TAAGGCAGACAGAAT | 100287144 |
| rs188143133 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210405 | AAGTCATGATGTGGG[A/C]TGTGTCTGTTGAATT | 100287144 |
| rs188241677 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209660 | ATACCTTCTGATTTC[A/T]CAAGATTTTTCTTTC | 100287144 |
| rs188297990 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209924 | AGCATTTCATGCAAA[C/G]ACTTGTCTTGTTGTC | 100287144 |
| rs188392761 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209461 | AGACAGGGCCTCACT[G/T]CCGTCCGCCGGGCTA | 100287144 |
| rs188408246 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210202 | AACACACATACACAC[A/G]CGCCCCCCCCCACAC | 100287144 |
| rs188713313 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212674 | AGTTGTTGGTCGGCA[C/T]GAGAAGGTGAAATTT | 100287144 |
| rs188798303 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208790 | ACCCTGTGGGAAGCC[A/T]CGGCATCTGGATTGC | 100287144 |
| rs188888630 | snp | C/G | 0.0322114 | 0.122752 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212416 | CCCAAGTTTCTGTCT[C/G]TACAACAGGGACAAC | 100287144 |
| rs189033959 | snp | A/G/T | 0.00349783 | 0.0416793 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210757 | TTGCTGAAATCCAGC[A/G/T]TACTTCTCTCCCTGA | 100287144 |
| rs189115338 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209373 | TCCCACTGAAACAAG[A/G]ACCAGTATTAAAAAT | 100287144 |
| rs189174316 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210109 | TCAGAAAGCACACTT[C/T]CGAATTCTTGTCCTT | 100287144 |
| rs189629846 | snp | A/C | 0.000357814 | 0.0133708 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210965 | GACATACAAACCGCC[A/C]CTTGCCAACTACATG | 100287144 |
| rs189762637 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208844 | CTGAAAATCGTGGCT[C/G]CTTTCTCCCTGTGTA | 100287144 |
| rs189775958 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210101 | TTCTCAGGTCAGAAA[A/G]CACACTTCCGAATTC | 100287144 |
| rs189915097 | snp | A/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209959 | GGCAAGTAATTCAAC[A/T]CGGATAGAGAATCAA | 100287144 |
| rs189956136 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210068 | TACGCTGTGCTAAAT[A/G]TTATACTTCATTGAC | 100287144 |
| rs190035450 | snp | C/G | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209861 | CAAACTTCAGTGCTT[C/G]TTTCTACCATATGAT | 100287144 |
| rs190263201 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209257 | CAAATGTGCTAACTG[C/G]AATTCCACCATACAA | 100287144 |
| rs190554546 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208984 | GGGCCAAAGGTCACA[C/G]TCCTCTCATTCCATC | 100287144 |
| rs190685821 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209467 | GGCCTCACTGCCGTC[A/C]GCCGGGCTATCTAGA | 100287144 |
| rs190696563 | snp | C/T | 0.0124255 | 0.0778353 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211843 | CAAGAGCCCTTGGCG[C/T]AGAAGACACAGACAG | 100287144 |
| rs190813900 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210536 | GGTTGGTGTGGGTGA[C/G]TTATAGAAGGGCTGA | 100287144 |
| rs191017496 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209005 | TCATTCCATCATACT[A/C]CTTAAAATCATCCTA | 100287144 |
| rs191118388 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208888 | CAGTGCTCCTTTCTT[C/G]CCACAGGAAACTTTA | 100287144 |
| rs191192619 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209393 | GTATTAAAAATGGTA[C/T]GCTATACTCTGTTTC | 100287144 |
| rs191387875 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209872 | GCTTCTTTCTACCAT[A/T]TGATGCTTTATCATT | 100287144 |
| rs191405498 | snp | A/G | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212164 | AGTCCATGAACACTG[A/G]CACACTCGCTTCCCT | 100287144 |
| rs191550242 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210487 | GATATTTGATTGGCT[A/T]ATCGCGCACCTGATG | 100287144 |
| rs191624460 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210246 | CACACACACACACAC[A/T]CACACGGTTTCCAAG | 100287144 |
| rs191956788 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209443 | CTCCGATGTTTCTTC[C/T]TGAGACAGGGCCTCA | 100287144 |
| rs192066609 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209179 | GAATGAAGACACACC[A/C]AAATTCTGTCCCTCT | 100287144 |
| rs192119522 | snp | C/T | 0.000191957 | 0.00979498 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211079 | CCACATTCCTGGCCA[C/T]GTCATCCAGCCCTCA | 100287144 |
| rs192321728 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209543 | TTCGTCTCTATGAAA[C/T]GTTGATCCATTATCA | 100287144 |
| rs192740929 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209124 | AGACATGTTGGGAAA[A/G]TCCCAAGAGCCAGGA | 100287144 |
| rs192898468 | snp | A/C | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210113 | AAAGCACACTTCCGA[A/C]TTCTTGTCCTTCGGT | 100287144 |
| rs193189159 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209788 | TCAAATAGTCTCCCG[A/C]TGATTGCATGATTCC | 100287144 |
| rs193227739 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212283 | CCCACACGTAGGGGT[G/T]CATACACACACACAC | 100287144 |
| rs200096337 | in-del | -/ACAT | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212313 | CACACACACACACAC[-/ACAT]AACTACACCCAGAAG | 100287144 |
| rs200661664 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208900 | CTTCCCACAGGAAAC[-/TT]TACATCAGGCACAGG | 100287144 |
| rs201780477 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210352 | TCCTATTATATGTGC[-/T]TATCATCCTGAGGAG | 100287144 |
| rs367633941 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212740 | CCTTGAATAGTGGAA[A/G]CTGGAATGCATTTGG | 100287144 |