| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs749660204 | snp | C/T | 0.000467998 | 0.0152899 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446181 | CGCCCCCAGCCGCTC[C/T]CGAGCGTAGAAAGTG | 80700 |
| rs749786337 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452066 | AGGCACGAGAATCGT[C/T]TGAATCCAGGAGGCG | 80700 |
| rs749822999 | snp | C/T | 5.07129e-05 | 0.00503527 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446690 | GGGCCAAGGTGGTCT[C/T]GCTCAGCACGTAGAA | 80700 |
| rs749831001 | snp | A/G | 3.99505e-05 | 0.00446919 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452501 | CAGATACCTGGGGCG[A/G]TGAAAGCGTCCAAGT | 80700 |
| rs749832706 | snp | A/G | 3.07442e-05 | 0.0039206 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446203 | TAGAAAGTGCCTGGG[A/G]AGTGGGGGAGTCAGA | 80700 |
| rs749988682 | snp | C/T | 1.65105e-05 | 0.00287315 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445566 | GCTCGGCCCCCGCGG[C/T]CTTGATGTCCTCCAG | 80700 |
| rs750006304 | snp | A/G | 0.000166987 | 0.00913594 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457713 | GGTGGCGGCTGGCCC[A/G]GCGGCGGGGGGCCGC | 80700 |
| rs750066226 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454970 | CGCCACCCTCGTGGC[A/G]GGACCCTGGGGAGAG | 80700 |
| rs750103807 | snp | C/G | 3.66804e-05 | 0.00428239 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457617 | GTTCCTCACGCACCC[C/G]ACGGACTCTTTGAGC | 80700 |
| rs750257971 | in-del | -/GAGG | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454107 | CCCTGGGAACAGACC[-/GAGG]GAGAGTGAGTGTATC | 80700 |
| rs750303262 | snp | C/T | 1.66186e-05 | 0.00288254 | missense | UBXN6 | GRCh38.p7 | 19:4453987 | GGGACTGCTTCTGCT[C/T]CAGCCGGGCTAGGGC | 80700 |
| rs750312884 | snp | A/G | 1.69458e-05 | 0.00291078 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446713 | ACGTAGAACTCCTCG[A/G]GGTCCTCTACAGCGT | 80700 |
| rs750315970 | snp | C/G | 1.69527e-05 | 0.00291137 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446112 | CCCTCCCGAGGCCAG[C/G]AGCTCAAAAGGCAGC | 80700 |
| rs750345798 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452552 | ACCCCGACCCTCGCC[A/G]AGCACCACAGTCCTG | 80700 |
| rs750560368 | snp | A/G | 1.97424e-05 | 0.00314178 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445963 | CTCTGAGAACAAGGA[A/G]GCTCCCTCCTGGGGG | 80700 |
| rs750611562 | snp | A/T | 1.74108e-05 | 0.00295044 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446548 | GTGAGGTTGAAGAAG[A/T]CCCCAGGCAGTTCGA | 80700 |
| rs750616649 | snp | A/G/T | 0.000114343 | 0.00756042 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446483 | GCCCCACTCTGCTCC[A/G/T]CGGACGTCAGGCCCA | 80700 |
| rs750716593 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4448885 | GAGAGGCCCATCGTC[C/G]AGGGTCACAGGGATG | 80700 |
| rs750846488 | snp | C/T | 6.84943e-05 | 0.00585171 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446914 | CTTCCAGGCAGTTAA[C/T]GCGCTCCTGGGGGTG | 80700 |
| rs750985869 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447965 | AGCAGGGGGCTCCTG[C/T]GGGGTGCTCCCTCGG | 80700 |
| rs751064913 | snp | C/T | 4.32255e-05 | 0.00464875 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446169 | GAACCCGTACACCGC[C/T]CCCAGCCGCTCCCGA | 80700 |
| rs751130975 | snp | G/T | 1.79162e-05 | 0.00299295 | missense | UBXN6 | GRCh38.p7 | 19:4452488 | TCCTCTCTGGGCTCA[G/T]ATACCTGGGGCGGTG | 80700 |
| rs751237087 | snp | C/T | 1.67167e-05 | 0.00289103 | missense | UBXN6 | GRCh38.p7 | 19:4452414 | GGTCCTTCCTCAGGG[C/T]GGCCCCAGTGAGCGG | 80700 |
| rs751514282 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452765 | ACACGCAGGAAACAC[C/T]CAGCAGATGGCAGCT | 80700 |
| rs751578130 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454380 | TCATCTGTAAAATGG[A/G]GTGACAGCACCCCTC | 80700 |
| rs751909205 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445541 | AGCTCGGGTTTCAGG[A/G]TGGAGTCCGGCTCGG | 80700 |
| rs751965942 | snp | A/G | 0.000262378 | 0.0114508 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446367 | GCTCCTCCTTCTCCC[A/G]CATGGCCTTGGTCCG | 80700 |
| rs751997809 | snp | C/T | 0.000496222 | 0.0157437 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446409 | GCCGCTCCACCGCCT[C/T]GGACCTGCACACGCG | 80700 |
| rs752016310 | snp | A/G | 1.65002e-05 | 0.00287225 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447613 | GGGGTGCAGGTGGAT[A/G]TTGTCCAGGTACCTG | 80700 |
| rs752026101 | snp | A/G | 0.000176134 | 0.00938275 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457721 | CTGGCCCGGCGGCGG[A/G]GGGCCGCGGGGGCGG | 80700 |
| rs752034454 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449053 | TCATAGCTGGAACTC[G/T]GGGGGTTTCCCAGAA | 80700 |
| rs752062516 | in-del | -/CGGCGGCGGGGGGCCG | 5.48938e-05 | 0.00523869 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457712 | TGGTGGCGGCTGGCC[-/CGGCGGCGGGGGGCCG]CGGGGGCGGGGGGGC | 80700 |
| rs752066367 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449674 | TCAGGAGCTGGGTAC[A/G]TGCACAGACAAGGGA | 80700 |
| rs752067512 | snp | A/C | 1.65048e-05 | 0.00287265 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447553 | AGGCACGCCCACCTG[A/C]AACACCTTGTTCTGC | 80700 |
| rs752069457 | in-del | -/GCTGGGATGAGCTGGAGGGGC | 1.66244e-05 | 0.00288304 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448267 | CCCAGTGGGAGGGGT[-/GCTGGGATGAGCTGGAGGGGC]GCTGGGATGAGCTGG | 80700 |
| rs752239845 | snp | A/C/T | 3.31781e-05 | 0.00407286 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446811 | TCGTCCCCATTCCCT[A/C/T]CTCAGCCAGGCCCTG | 80700 |
| rs752388535 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450474 | CTAATATGTAAAGAG[C/T]GCTGCCGGGCACGGT | 80700 |
| rs752398883 | snp | G/T | 4.302e-05 | 0.00463769 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453424 | CTGTCCCCACCCCTT[G/T]GCATGGGACAGTGCC | 80700 |
| rs752403909 | snp | A/G | 1.69965e-05 | 0.00291513 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446743 | TGGCAGGACATGGGT[A/G]TCACTGTGCAATGGA | 80700 |
| rs752423204 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445084 | GGCCAGCATCCCCTC[C/T]TGCCGTTGTCACCCA | 80700 |
| rs752479381 | snp | A/G | 0.000417779 | 0.014447 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448457 | ACTCACTGAGAGCCC[A/G]GGCCGCACGGCCCTC | 80700 |
| rs752539913 | snp | G/T | 1.94945e-05 | 0.003122 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445970 | AACAAGGAGGCTCCC[G/T]CCTGGGGGTGTCTGT | 80700 |
| rs752655201 | in-del | -/CTCTGGGGA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452258 | ACTACTAGCAGTGGC[-/CTCTGGGGA]CTCTGGGAGGGATCT | 80700 |
| rs752661398 | in-del | -/C | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459089 | CAGCACTTTGGGAGG[-/C]CGAGGCCGGCGGATC | 80700 |
| rs752690839 | snp | A/G | 0.000235988 | 0.0108599 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444614 | AGGACACTGGGTCCC[A/G]GACCACCCAGGATCA | 80700 |
| rs752766527 | snp | A/C/G/T | 0.000128999 | 0.00803038 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446422 | CTCGGACCTGCACAC[A/C/G/T]CGGGCCAGGTCACGA | 80700 |
| rs752782451 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449891 | TCCAGCTGGATCAAA[A/G]CTTCAACCATGGAAA | 80700 |
| rs752843116 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454636 | AGCTCAGGCTGGTCT[C/T]GAACTTTTGCCTCAA | 80700 |
| rs752879886 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449190 | ATCACACACGGCCAC[A/G]CCCAGAGAGCCACCC | 80700 |
| rs752880749 | snp | C/G | 1.65015e-05 | 0.00287237 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447559 | GCCCACCTGAAACAC[C/G]TTGTTCTGCAGCTTG | 80700 |
| rs752927530 | snp | G/T | 1.66004e-05 | 0.00288096 | missense | UBXN6 | GRCh38.p7 | 19:4453977 | CCCCAGGCCCGGGAC[G/T]GCTTCTGCTCCAGCC | 80700 |
| rs752959433 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455996 | CCCTGGGACAGCAGA[A/G]GCCTTCTCCTGTCCA | 80700 |
| rs753101384 | snp | C/T | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446797 | TGCCCCGAGGCCCCT[C/T]GTCCCCATTCCCTAC | 80700 |
| rs753111928 | in-del | -/G | 1.93806e-05 | 0.00311286 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446945 | GAGATGGGCGTCACT[-/G]GGGGCCCCTGGCTTC | 80700 |
| rs753140624 | snp | C/T | 6.25176e-05 | 0.00559061 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446462 | GGGGTTCTTCCACCC[C/T]GCCCCGCCCCACTCT | 80700 |
| rs753164736 | in-del | -/T | 4.78297e-05 | 0.00489005 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446257 | CCAACCCGAGCCGCC[-/T]CTCCACGGGCATCGT | 80700 |
| rs753193487 | in-del | -/A | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445446 | GGCGGGGAGAGGAAC[-/A]AGGGAGAGCATGAGA | 80700 |
| rs753247555 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454857 | GGAGCTGGTCGGCTC[A/G]CTTGGTTTACTCCTC | 80700 |
| rs753345669 | in-del | -/G | 0.000246093 | 0.0110899 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457734 | GGGGGCCGCGGGGGC[-/G]GGGGGGGCACGGGGC | 80700 |
| rs753406687 | snp | A/C | 1.93112e-05 | 0.00310728 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457601 | GGCCTCAAGCCCCTG[A/C]GTTCCTCACGCACCC | 80700 |
| rs753495583 | in-del | -/TCT | 2.37982e-05 | 0.00344942 | cds-indel, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448376 | TGTTGAACGTGTAGA[-/TCT]TCATGATGGAGGCGG | 80700 |
| rs753575374 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457249 | CGTTCCACTGACCCC[-/C]AACTGCCTACAGCCC | 80700 |
| rs753606203 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450600 | CGTCTCTACTAAAAA[C/T]ACAAAGAATCAGCTG | 80700 |
| rs753612345 | snp | C/T | 0.000101598 | 0.00712663 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446661 | TTCCTTGTGCCTCTC[C/T]AGGCTCTGGGGCTGG | 80700 |
| rs753672836 | snp | A/C | 1.64762e-05 | 0.00287016 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446103 | CAGCTTCTGCCCTCC[A/C]GAGGCCAGCAGCTCA | 80700 |
| rs753848499 | snp | C/T | 3.53632e-05 | 0.0042048 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446523 | CTGCTCCCGCTTGAT[C/T]TCCTCTGCTGTGAGG | 80700 |
| rs753990757 | snp | C/T | 5.7374e-05 | 0.00535572 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446467 | TCTTCCACCCCGCCC[C/T]GCCCCACTCTGCTCC | 80700 |
| rs754011124 | in-del | -/TCC | 1.69218e-05 | 0.00290871 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446080 | AAGGCCAGGTTCTCG[-/TCC]TCGGACAGCTTCTGC | 80700 |
| rs754025089 | in-del | -/CTC | 0.000123939 | 0.00787109 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446523 | CTGCTCCCGCTTGAT[-/CTC]CTCTGCTGTGAGGTT | 80700 |
| rs754119894 | snp | C/T | 1.70203e-05 | 0.00291716 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454028 | GCCATCTGTGCCTCA[C/T]TGGTGGGTCCCTGGC | 80700 |
| rs754169051 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451284 | CTGGTCTTGGAACTT[C/G]TGACCTCAGGTGATC | 80700 |
| rs754188647 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459566 | AAAAAGGCCAGGCAC[A/G]GTGGCTCATGCCTGT | 80700 |
| rs754221360 | snp | A/G | 4.17388e-05 | 0.00456812 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446234 | GCGGGTGGGGCCCAG[A/G]GCCCCCTACCAACCC | 80700 |
| rs754248747 | snp | A/G | 1.66521e-05 | 0.00288544 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446893 | CCTCAAAAAACTCGT[A/G]GGTCCCTTCCAGGCA | 80700 |
| rs754262417 | snp | A/G | 2.08067e-05 | 0.00322535 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453434 | CCCTTGGCATGGGAC[A/G]GTGCCACCAGTGGCT | 80700 |
| rs754300067 | snp | C/T | 3.31252e-05 | 0.00406958 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446825 | TACTCAGCCAGGCCC[C/T]GTCCACTTACCCTGA | 80700 |
| rs754364213 | snp | A/C | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448664 | CCTTCTCAAGGCTAG[A/C]TCCATGGGACTTGGA | 80700 |
| rs754423009 | snp | C/T | 2.25071e-05 | 0.00335455 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446172 | CCCGTACACCGCCCC[C/T]AGCCGCTCCCGAGCG | 80700 |
| rs754611823 | snp | A/C/T | 0.00015524 | 0.00880903 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446132 | CAAAAGGCAGCCAGT[A/C/T]GCTCTGCAGGGCCTC | 80700 |
| rs754632715 | in-del | -/A | 1.66599e-05 | 0.00288611 | splice-donor-variant | UBXN6 | GRCh38.p7 | 19:4452362 | CACAGGGTGCCACTC[-/A]CCAAGAGAATGGCCT | 80700 |
| rs754649740 | snp | A/G | 3.3961e-05 | 0.0041206 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446727 | GGGGTCCTCTACAGC[A/G]TGGCAGGACATGGGT | 80700 |
| rs754674686 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454152 | GCCGGCAAAGCTGAC[A/G]TGCAGTCACACAGAG | 80700 |
| rs754696965 | snp | A/T | 1.79094e-05 | 0.00299239 | missense | UBXN6 | GRCh38.p7 | 19:4452489 | CCTCTCTGGGCTCAG[A/T]TACCTGGGGCGGTGA | 80700 |
| rs754760001 | snp | C/T | 2.42222e-05 | 0.00348001 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448352 | CCAGCTTCACCCGGT[C/T]CTGGTCTTTGTTGAA | 80700 |
| rs754920309 | snp | G/T | 1.71199e-05 | 0.00292569 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454034 | TGTGCCTCATTGGTG[G/T]GTCCCTGGCGGGGCG | 80700 |
| rs754963132 | snp | A/G | 8.28912e-05 | 0.00643729 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448300 | GGGCCAGGCAGGGCA[A/G]AGGGGCCACACGCTC | 80700 |
| rs754996768 | snp | C/T | 1.65037e-05 | 0.00287256 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447556 | CACGCCCACCTGAAA[C/T]ACCTTGTTCTGCAGC | 80700 |
| rs755186878 | snp | C/G | 1.70615e-05 | 0.00292069 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453889 | CAGGGCCGAGAACCT[C/G]AAACAGCCCCAACCT | 80700 |
| rs755247775 | snp | C/G | | | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448215 | CTCCTTCCCAACCCA[C/G]CTCAGCAGGTAATGA | 80700 |
| rs755248614 | snp | A/G | 1.67539e-05 | 0.00289425 | missense | UBXN6 | GRCh38.p7 | 19:4452416 | TCCTTCCTCAGGGTG[A/G]CCCCAGTGAGCGGAC | 80700 |
| rs755271636 | snp | C/G | 3.69549e-05 | 0.00429838 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446017 | CCTGCAGAGGCATCG[C/G]GTCAGCGGTGCTCCT | 80700 |
| rs755312992 | in-del | -/T | 0.000122005 | 0.00780947 | frameshift-variant, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446136 | GGCAGCCAGTCGCTC[-/T]TGCAGGGCCTCCCGG | 80700 |
| rs755420633 | snp | A/G | 4.47618e-05 | 0.00473063 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446410 | CCGCTCCACCGCCTC[A/G]GACCTGCACACGCGG | 80700 |
| rs755527431 | snp | C/G | 0.000253867 | 0.0112636 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454109 | CTGGGAACAGACCGA[C/G]GGAGAGTGAGTGTAT | 80700 |
| rs755544978 | snp | A/G | 0.000151649 | 0.00870641 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446372 | TCCTTCTCCCGCATG[A/G]CCTTGGTCCGCAGCA | 80700 |
| rs755597683 | in-del | -/GG | 5.00513e-05 | 0.00500231 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448283 | CTGGGATGAGCTGGA[-/GG]GGGGCCAGGCAGGGC | 80700 |
| rs755598447 | snp | C/G | 3.54296e-05 | 0.00420875 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457641 | TTTGAGCTTCTGACC[C/G]GGTCCCGCGCTCTTG | 80700 |
| rs755604057 | snp | A/C/T | 0.000319692 | 0.0126393 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448311 | GGCAAAGGGGCCACA[A/C/T]GCTCACTTGGCAATG | 80700 |
| rs755651112 | snp | A/T | 1.71997e-05 | 0.0029325 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454040 | TCATTGGTGGGTCCC[A/T]GGCGGGGCGGCCTGG | 80700 |
| rs755721228 | in-del | -/CG | 4.31202e-05 | 0.00464308 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446421 | CCTCGGACCTGCACA[-/CG]CGGGCCAGGTCACGA | 80700 |
| rs755883529 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450529 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 80700 |
| rs755908283 | snp | C/T | 1.94725e-05 | 0.00312023 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445971 | ACAAGGAGGCTCCCT[C/T]CTGGGGGTGTCTGTG | 80700 |
| rs755988167 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444618 | CACTGGGTCCCGGAC[C/G]ACCCAGGATCATCTC | 80700 |
| rs756042421 | snp | A/G | 0.000189372 | 0.00972882 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448369 | TGGTCTTTGTTGAAC[A/G]TGTAGATCTTCATGA | 80700 |
| rs756076182 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445120 | ACAGAGCAGCCCTAG[C/T]GCCAGGTGCAGCCAC | 80700 |
| rs756245428 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456688 | CCTCCCTAGACAATC[C/G]GGAAGCCTGCCCGGC | 80700 |
| rs756273898 | snp | C/G | 1.65072e-05 | 0.00287286 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447628 | GTTGTCCAGGTACCT[C/G]GGGTAGGTGGAGAAG | 80700 |
| rs756313078 | snp | A/G | 4.87936e-05 | 0.00493907 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446384 | ATGGCCTTGGTCCGC[A/G]GCACGCTCAGCCGCT | 80700 |
| rs756335250 | snp | C/G | | | missense | UBXN6 | GRCh38.p7 | 19:4453978 | CCCAGGCCCGGGACT[C/G]CTTCTGCTCCAGCCG | 80700 |
| rs756394194 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447563 | ACCTGAAACACCTTG[C/T]TCTGCAGCTTGATCT | 80700 |
| rs756402198 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454665 | AAATGATCCTCCCAC[C/T]GTGGCCTCCCAAACT | 80700 |
| rs756428025 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449916 | TGGAAACAAGCAAGC[A/G]GTCAAGGAGAAGCCA | 80700 |
| rs756483729 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456092 | TCCACAAGGGACCTC[C/T]GCACCGCTTCCTTTC | 80700 |
| rs756493441 | snp | A/C | 0.000106411 | 0.00729344 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453427 | TCCCCACCCCTTGGC[A/C]TGGGACAGTGCCACC | 80700 |
| rs756578803 | snp | G/T | 1.67192e-05 | 0.00289125 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445658 | TCACTCTGAGACCGA[G/T]AGTCGGCCCTTGCCG | 80700 |
| rs756616365 | snp | A/G | 4.81661e-05 | 0.00490721 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446288 | TGGTGCCCACCCTGC[A/G]GGAGGCAGCCATCGG | 80700 |
| rs756679868 | snp | C/T | 3.66233e-05 | 0.00427906 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452499 | CTCAGATACCTGGGG[C/T]GGTGAAAGCGTCCAA | 80700 |
| rs756701594 | snp | C/T | 4.99863e-05 | 0.00499906 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448463 | TGAGAGCCCGGGCCG[C/T]ACGGCCCTCCGCTGC | 80700 |
| rs756954733 | snp | A/G | 5.46314e-05 | 0.00522616 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454121 | CGAGGGAGAGTGAGT[A/G]TATCCTCCCGAGGTG | 80700 |
| rs756956934 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454859 | AGCTGGTCGGCTCGC[G/T]TGGTTTACTCCTCCT | 80700 |
| rs756990453 | snp | A/G | 4.82265e-05 | 0.00491029 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446289 | GGTGCCCACCCTGCA[A/G]GAGGCAGCCATCGGG | 80700 |
| rs757032577 | snp | C/T | 1.70153e-05 | 0.00291674 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453902 | CTCAAACAGCCCCAA[C/T]CTGGGCCCGAGGAGG | 80700 |
| rs757115612 | snp | G/T | 1.82061e-05 | 0.00301708 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446029 | TCGGGTCAGCGGTGC[G/T]CCTGCGGGCCGACAC | 80700 |
| rs757141712 | snp | A/G | 0.000118486 | 0.00769605 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446104 | AGCTTCTGCCCTCCC[A/G]AGGCCAGCAGCTCAA | 80700 |
| rs757170282 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450630 | GGGCGTGGTGGCGGT[G/T]CGCCTGTGGTCCCAG | 80700 |
| rs757170638 | snp | C/T | 1.71705e-05 | 0.00293001 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446601 | CTGGAAGACGCGGCG[C/T]TGCCTGTCCAGCTTG | 80700 |
| rs757238267 | snp | A/G | 0.000160659 | 0.00896122 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452503 | GATACCTGGGGCGGT[A/G]AAAGCGTCCAAGTCT | 80700 |
| rs757396756 | snp | C/G | 2.73459e-05 | 0.0036976 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446469 | TTCCACCCCGCCCCG[C/G]CCCACTCTGCTCCGC | 80700 |
| rs757451645 | snp | A/G | 4.93815e-05 | 0.00496873 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448285 | TGGGATGAGCTGGAG[A/G]GGCCAGGCAGGGCAA | 80700 |
| rs757496193 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451294 | AACTTCTGACCTCAG[A/G]TGATCCACCTGCCTC | 80700 |
| rs757601709 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447792 | TCCGGGTGGAAGGCA[C/T]ACCTCGGACACCCCA | 80700 |
| rs757627514 | snp | A/G | 1.6884e-05 | 0.00290547 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446906 | GTGGGTCCCTTCCAG[A/G]CAGTTAATGCGCTCC | 80700 |
| rs757629381 | snp | C/T | 4.35246e-05 | 0.00466481 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446240 | GGGGCCCAGGGCCCC[C/T]TACCAACCCGAGCCG | 80700 |
| rs757721646 | in-del | -/AG | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444918 | TGGTCCCACCTTGAC[-/AG]GGAGCCACACCCAGC | 80700 |
| rs757823932 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446826 | ACTCAGCCAGGCCCT[A/G]TCCACTTACCCTGAT | 80700 |
| rs757824689 | snp | A/T | 2.06703e-05 | 0.00321477 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453436 | CTTGGCATGGGACAG[A/T]GCCACCAGTGGCTGT | 80700 |
| rs757835676 | snp | C/T | 1.69229e-05 | 0.00290881 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446665 | TTGTGCCTCTCCAGG[C/T]TCTGGGGCTGGGCCA | 80700 |
| rs758062700 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445501 | CCTGCTTTTATTTCA[C/T]AAGAGCTTCTCGATG | 80700 |
| rs758087151 | snp | C/T | 3.37496e-05 | 0.00410775 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452313 | CGATGGAGGGTGGCT[C/T]AGGCACAGGAAGCTA | 80700 |
| rs758111104 | snp | G/T | 0.000165659 | 0.00909956 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457714 | GTGGCGGCTGGCCCG[G/T]CGGCGGGGGGCCGCG | 80700 |
| rs758150645 | snp | A/G | 3.27038e-05 | 0.00404361 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446209 | GTGCCTGGGGAGTGG[A/G]GGAGTCAGAGCGGGT | 80700 |
| rs758153656 | snp | A/G | 1.65111e-05 | 0.0028732 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447635 | AGGTACCTGGGGTAG[A/G]TGGAGAAGGTGAGTG | 80700 |
| rs758210155 | snp | A/G | 1.70694e-05 | 0.00292137 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454031 | ATCTGTGCCTCATTG[A/G]TGGGTCCCTGGCGGG | 80700 |
| rs758250064 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452693 | ATGTCAAATGTCCCT[A/G]TGGGGCCTGCTCAGA | 80700 |
| rs758286321 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451544 | TTTTTGGCAGAGACA[C/G]GGTTTTGCCATGTTG | 80700 |
| rs758300696 | snp | A/G | 1.69706e-05 | 0.0029129 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446114 | CTCCCGAGGCCAGCA[A/G]CTCAAAAGGCAGCCA | 80700 |
| rs758407048 | snp | C/T | 1.66197e-05 | 0.00288263 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453988 | GGACTGCTTCTGCTC[C/T]AGCCGGGCTAGGGCG | 80700 |
| rs758461961 | snp | A/C | 1.66729e-05 | 0.00288724 | missense | UBXN6 | GRCh38.p7 | 19:4453930 | AGGGCCATATCTCAC[A/C]CTGGTTTCGGATGGT | 80700 |
| rs758531878 | snp | C/G | 1.96663e-05 | 0.00313572 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445965 | CTGAGAACAAGGAGG[C/G]TCCCTCCTGGGGGTG | 80700 |
| rs758546218 | snp | A/C/G | 7.76433e-05 | 0.00623029 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453450 | GTGCCACCAGTGGCT[A/C/G]TTCTTACCACGTTGG | 80700 |
| rs758623562 | snp | C/T | 5.20359e-05 | 0.00510051 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446363 | CGCTGCTCCTCCTTC[C/T]CCCGCATGGCCTTGG | 80700 |
| rs758643772 | snp | G/T | 1.81618e-05 | 0.0030134 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457621 | CTCACGCACCCCACG[G/T]ACTCTTTGAGCTTCT | 80700 |
| rs758771869 | snp | A/G | 1.65658e-05 | 0.00287795 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445449 | CGGGGAGAGGAACAG[A/G]GAGAGCATGAGACAG | 80700 |
| rs758946725 | in-del | -/CTC | 5.42255e-05 | 0.00520671 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446353 | GCGCAGCCCCCGCTG[-/CTC]CTCCTTCTCCCGCAT | 80700 |
| rs758962723 | snp | A/G | 4.95724e-05 | 0.00497833 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446302 | CAGGAGGCAGCCATC[A/G]GGGAGGCGCACGCGC | 80700 |
| rs758984301 | snp | A/G | 3.4632e-05 | 0.00416111 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446917 | CCAGGCAGTTAATGC[A/G]CTCCTGGGGGTGGAG | 80700 |
| rs759070495 | snp | C/T | 4.19182e-05 | 0.00457792 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445942 | GGGACCTGCCCAGGC[C/T]CCCTGCTCTGAGAAC | 80700 |
| rs759095056 | snp | A/G | 2.17059e-05 | 0.00329431 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453417 | AGTCAAGCTGTCCCC[A/G]CCCCTTGGCATGGGA | 80700 |
| rs759293083 | snp | A/G | 3.3134e-05 | 0.00407012 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447675 | CCAGGCTGCCCACCC[A/G]GCCCCTCTGTGCCTC | 80700 |
| rs759353137 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458815 | AGCTTGCAGTGAGCC[A/G]AGATCTCACCACTGC | 80700 |
| rs759367896 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454535 | TCAAGGAATCCTCCC[A/G]CCTCAGCCTCCCAAG | 80700 |
| rs759382212 | snp | A/G | 5.14708e-05 | 0.00507274 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446328 | CGCGCAGCAGCGTGT[A/G]GTTGTACTTGCGCAG | 80700 |
| rs759512258 | snp | A/C | 1.81148e-05 | 0.0030095 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454106 | TCCCTGGGAACAGAC[A/C]GAGGGAGAGTGAGTG | 80700 |
| rs759544723 | snp | A/G | 1.65963e-05 | 0.0028806 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446883 | AACCCAATGGCCTCA[A/G]AAAACTCGTGGGTCC | 80700 |
| rs759550086 | snp | C/T | 1.66051e-05 | 0.00288137 | missense | UBXN6 | GRCh38.p7 | 19:4453971 | GTGGGGCCCCAGGCC[C/T]GGGACTGCTTCTGCT | 80700 |
| rs759618421 | in-del | -/TCTC | | | intron-variant, upstream-variant-2KB, frameshift-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444564 | CGCAGCCTCTTCCAG[-/TCTC]TCTCTGATTCACCCT | 80700 |
| rs759653428 | in-del | -/GCTACT | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450645 | TCGCCTGTGGTCCCA[-/GCTACT]CGGGAGGCTGAGGCA | 80700 |
| rs759710735 | in-del | -/A | 1.65496e-05 | 0.00287655 | frameshift-variant, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446855 | TCCTGGGCGGGAAGC[-/A]AACACCTTCTGGAAC | 80700 |
| rs759783627 | in-del | -/AA | 1.88542e-05 | 0.0030703 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453540 | GGAAGGCAGCCCAAG[-/AA]AGAGAGGCAGAGACG | 80700 |
| rs759798589 | snp | C/T | 3.37838e-05 | 0.00410984 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446094 | GTCCTCGGACAGCTT[C/T]TGCCCTCCCGAGGCC | 80700 |
| rs759855616 | snp | C/G | 1.69585e-05 | 0.00291187 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446652 | CAGCAGCTGTTCCTT[C/G]TGCCTCTCCAGGCTC | 80700 |
| rs760009900 | snp | C/T | 1.65556e-05 | 0.00287707 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447672 | AGCCCAGGCTGCCCA[C/T]CCGGCCCCTCTGTGC | 80700 |
| rs760010141 | snp | C/G | 0.000278697 | 0.0118013 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446449 | ACGAGGGCTGGCCGG[C/G]GTTCTTCCACCCCGC | 80700 |
| rs760034843 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449750 | TACTTTGTGAGAAAG[A/G]TGGGATTTCACAGCT | 80700 |
| rs760071185 | snp | G/T | 4.94996e-05 | 0.00497467 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447615 | GGTGCAGGTGGATGT[G/T]GTCCAGGTACCTGGG | 80700 |
| rs760164843 | snp | A/G | 0.000192938 | 0.00981998 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446274 | TCCACGGGCATCGTT[A/G]GTGCCCACCCTGCAG | 80700 |
| rs760246216 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449491 | GATGATGTGGGGAGC[A/G]GGACAGAGCACGTGG | 80700 |
| rs760322736 | snp | A/G | 1.91716e-05 | 0.00309603 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445984 | CTCCTGGGGGTGTCT[A/G]TGCCGGTCCCAGGAG | 80700 |
| rs760327455 | snp | A/C | 1.65787e-05 | 0.00287907 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447515 | AGCTGCCCCCACCCC[A/C]AGCCTGGGCCCCGGG | 80700 |
| rs760364352 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451789 | ATTACAGGCATGTGC[C/T]ACCATGCCTGGCTAA | 80700 |
| rs760378707 | snp | C/T | 1.66324e-05 | 0.00288374 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446890 | TGGCCTCAAAAAACT[C/T]GTGGGTCCCTTCCAG | 80700 |
| rs760432660 | snp | C/T | 6.60327e-05 | 0.00574561 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445561 | GTCCGGCTCGGCCCC[C/T]GCGGCCTTGATGTCC | 80700 |
| rs760437963 | snp | C/T | 3.59479e-05 | 0.00423942 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453485 | TGGGGCCTCGGGGCT[C/T]CCGCTGACGGTGGCT | 80700 |
| rs760510578 | snp | A/G | | | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445998 | TGTGCCGGTCCCAGG[A/G]GAACCTGCAGAGGCA | 80700 |
| rs760596247 | snp | C/T | 1.67013e-05 | 0.0028897 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457693 | TCCTGAAAGAATTTC[C/T]TCATGGTGGCGGCTG | 80700 |
| rs760617326 | snp | A/C | 1.65045e-05 | 0.00287263 | stop-lost, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445499 | ACCCTGCTTTTATTT[A/C]ACAAGAGCTTCTCGA | 80700 |
| rs760652207 | snp | A/G | 4.73967e-05 | 0.00486787 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448459 | TCACTGAGAGCCCGG[A/G]CCGCACGGCCCTCCG | 80700 |
| rs760674587 | snp | C/T | 0.000108897 | 0.00737811 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446345 | TTGTACTTGCGCAGC[C/T]CCCGCTGCTCCTCCT | 80700 |
| rs760695831 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455782 | TGGAAAGGGCTAGAG[C/T]TGCCGCAGGGAGAGA | 80700 |
| rs760703814 | snp | A/G | 1.99962e-05 | 0.00316191 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457593 | CCCCGCAGGGCCTCA[A/G]GCCCCTGCGTTCCTC | 80700 |
| rs760741166 | in-del | -/GAA | 1.74637e-05 | 0.00295492 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446541 | CTCTGCTGTGAGGTT[-/GAA]GAAGTCCCCAGGCAG | 80700 |
| rs760941369 | snp | C/T | 1.69421e-05 | 0.00291046 | utr-variant-5-prime, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454018 | GGCAGCGGCTGCCAT[C/T]TGTGCCTCATTGGTG | 80700 |
| rs760953914 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449712 | ACAGCAGCCAGGAAG[A/G]GGTCCAAATCCATAC | 80700 |
| rs760964032 | snp | A/G | 1.66454e-05 | 0.00288486 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446788 | GGGCCCTCCTGCCCC[A/G]AGGCCCCTCGTCCCC | 80700 |
| rs761082765 | snp | C/T | 2.05975e-05 | 0.0032091 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445948 | TGCCCAGGCCCCCTG[C/T]TCTGAGAACAAGGAG | 80700 |
| rs761106610 | snp | C/T | 2.63328e-05 | 0.00362846 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448337 | CAATGGTGTCCACAC[C/T]CAGCTTCACCCGGTC | 80700 |
| rs761189258 | snp | A/C/G | 0.000460886 | 0.0151737 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446463 | GGGTTCTTCCACCCC[A/C/G]CCCCGCCCCACTCTG | 80700 |
| rs761256542 | snp | C/T | 5.20874e-05 | 0.00510304 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457710 | CATGGTGGCGGCTGG[C/T]CCGGCGGCGGGGGGC | 80700 |
| rs761265766 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455825 | TTTCCCCACAGCTGA[A/G]TCTCACTGTGTCCTG | 80700 |
| rs761284406 | snp | C/G | 9.8987e-05 | 0.00703447 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445517 | AAGAGCTTCTCGATG[C/G]CTGACAGGAGCTCGG | 80700 |
| rs761524177 | snp | C/G | 0.000369891 | 0.0135944 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446355 | GCAGCCCCCGCTGCT[C/G]CTCCTTCTCCCGCAT | 80700 |
| rs761580414 | snp | A/C/G | 0.000101711 | 0.00713066 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446712 | CACGTAGAACTCCTC[A/C/G]GGGTCCTCTACAGCG | 80700 |
| rs761640078 | snp | C/G | | | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446134 | AAAGGCAGCCAGTCG[C/G]TCTGCAGGGCCTCCC | 80700 |
| rs761716762 | snp | A/G | 3.46981e-05 | 0.00416508 | missense | UBXN6 | GRCh38.p7 | 19:4452462 | CAGGCACAGCCAGGT[A/G]GGCAGAGCCTTCCTC | 80700 |
| rs761810994 | snp | A/C/T | 6.76418e-05 | 0.00581518 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446678 | GGCTCTGGGGCTGGG[A/C/T]CAAGGTGGTCTCGCT | 80700 |
| rs761826290 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457198 | TCTCCCTCACCACCC[A/G]GCTCAGGACTCATGA | 80700 |
| rs762081150 | snp | G/T | 2.56815e-05 | 0.00358331 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448340 | TGGTGTCCACACCCA[G/T]CTTCACCCGGTCCTG | 80700 |
| rs762216104 | snp | G/T | 1.64754e-05 | 0.00287009 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453491 | CTCGGGGCTCCCGCT[G/T]ACGGTGGCTTCGGCT | 80700 |
| rs762251151 | snp | C/T | 6.89014e-05 | 0.00586907 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446594 | GCGAGGGCTGGAAGA[C/T]GCGGCGCTGCCTGTC | 80700 |
| rs762263493 | in-del | -/G | 0.000175793 | 0.00937367 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457718 | GGCTGGCCCGGCGGC[-/G]GGGGGGCCGCGGGGG | 80700 |
| rs762277377 | snp | A/G | 1.90612e-05 | 0.00308711 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445989 | GGGGGTGTCTGTGCC[A/G]GTCCCAGGAGAACCT | 80700 |
| rs762296904 | snp | C/T | 1.70348e-05 | 0.00291841 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446069 | CGCACTCGTTCAAGG[C/T]CAGGTTCTCGTCCTC | 80700 |
| rs762310505 | snp | C/T | 1.75526e-05 | 0.00296243 | missense | UBXN6 | GRCh38.p7 | 19:4452473 | AGGTGGGCAGAGCCT[C/T]CCTCTCTGGGCTCAG | 80700 |
| rs762486253 | snp | A/G | 7.36988e-05 | 0.00606992 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446444 | AGGTCACGAGGGCTG[A/G]CCGGGGTTCTTCCAC | 80700 |
| rs762539164 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447666 | GGGCACAGCCCAGGC[C/T]GCCCACCCGGCCCCT | 80700 |
| rs762610877 | snp | C/T | 3.32773e-05 | 0.00407892 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445641 | GCGGTAGGGGTAGGC[C/T]GTCACTCTGAGACCG | 80700 |
| rs762663986 | snp | C/T | 3.30262e-05 | 0.0040635 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445572 | CCCCCGCGGCCTTGA[C/T]GTCCTCCAGCACAGC | 80700 |
| rs762693408 | snp | C/T | 0.000599479 | 0.0173026 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446404 | GCTCAGCCGCTCCAC[C/T]GCCTCGGACCTGCAC | 80700 |
| rs762910074 | snp | A/G | 1.69438e-05 | 0.00291061 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446714 | CGTAGAACTCCTCGG[A/G]GTCCTCTACAGCGTG | 80700 |
| rs763030325 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453425 | TGTCCCCACCCCTTG[A/G]CATGGGACAGTGCCA | 80700 |
| rs763163672 | snp | A/G | 1.8592e-05 | 0.00304888 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446013 | AGAACCTGCAGAGGC[A/G]TCGGGTCAGCGGTGC | 80700 |
| rs763164461 | snp | C/T | 1.65419e-05 | 0.00287588 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445476 | ACAGACCCACAGGGC[C/T]GAGGCCAACCCTGCT | 80700 |
| rs763240896 | in-del | -/C | 1.76565e-05 | 0.00297118 | utr-variant-5-prime, frameshift-variant | UBXN6 | GRCh38.p7 | 19:4454072 | GGCTGGCTGGTTGGG[-/C]TTCTCTTTGTGGGCC | 80700 |
| rs763270697 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454279 | GGTTCTACTGCAGGC[A/G]GAAGAGCCCCTGGAG | 80700 |
| rs763296686 | snp | C/G | 3.99194e-05 | 0.00446745 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448449 | GGAAAGCCACTCACT[C/G]AGAGCCCGGGCCGCA | 80700 |
| rs763312462 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447610 | CTCGGGGTGCAGGTG[A/G]ATGTTGTCCAGGTAC | 80700 |
| rs763354592 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449602 | CCAGCCAAGGGAAGC[A/G]TGTCAGCTCCAAAAG | 80700 |
| rs763386494 | snp | C/T | 3.38719e-05 | 0.00411519 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446078 | TCAAGGCCAGGTTCT[C/T]GTCCTCGGACAGCTT | 80700 |
| rs763440281 | in-del | -/G | 1.65448e-05 | 0.00287613 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447527 | CCCAGCCTGGGCCCC[-/G]GGGGGCCAGAAGGCA | 80700 |
| rs763463983 | snp | C/T | 5.40001e-05 | 0.00519587 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446348 | TACTTGCGCAGCCCC[C/T]GCTGCTCCTCCTTCT | 80700 |
| rs763489258 | snp | A/G | 8.75427e-05 | 0.00661541 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453573 | GATAGTGAGCACGCC[A/G]CTGTCCTGGCCCAAG | 80700 |
| rs763606831 | snp | C/T | 0.000447327 | 0.0149487 | intron-variant, upstream-variant-2KB, synonymous-codon, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444584 | CTCTGATTCACCCTC[C/T]TGCCACCTCTTGTGA | 80700 |
| rs763660126 | snp | A/G | 1.66449e-05 | 0.00288482 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446275 | CCACGGGCATCGTTG[A/G]TGCCCACCCTGCAGG | 80700 |
| rs763663955 | snp | A/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454851 | CTGCTGGGAGCTGGT[A/C]GGCTCGCTTGGTTTA | 80700 |
| rs763677691 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452064 | TGAGGCACGAGAATC[A/G]TTTGAATCCAGGAGG | 80700 |
| rs763701564 | snp | A/G | 3.31087e-05 | 0.00406857 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447523 | CCACCCCCAGCCTGG[A/G]CCCCGGGGGCCAGAA | 80700 |
| rs763844334 | snp | C/T | 7.14937e-05 | 0.00597844 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446039 | GGTGCTCCTGCGGGC[C/T]GACACTCACCAGCCC | 80700 |
| rs763888668 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455819 | GGCAGATTTCCCCAC[A/G]GCTGAGTCTCACTGT | 80700 |
| rs763965653 | snp | C/T | 1.66078e-05 | 0.00288161 | missense | UBXN6 | GRCh38.p7 | 19:4452386 | ATGGCCTCCTTGATG[C/T]AGGCGTCCCGCTGGT | 80700 |
| rs763970890 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445158 | CACGGCACACGGGAA[C/T]AGGACCCATGCTGCA | 80700 |
| rs763974738 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445512 | TTCACAAGAGCTTCT[C/T]GATGGCTGACAGGAG | 80700 |
| rs764009181 | snp | C/T | 4.78183e-05 | 0.00488946 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448461 | ACTGAGAGCCCGGGC[C/T]GCACGGCCCTCCGCT | 80700 |
| rs764089706 | snp | C/G | 2.24384e-05 | 0.00334943 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457695 | CTGAAAGAATTTCTT[C/G]ATGGTGGCGGCTGGC | 80700 |
| rs764193289 | snp | A/C | 7.82707e-05 | 0.00625534 | synonymous-codon, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448338 | AATGGTGTCCACACC[A/C]AGCTTCACCCGGTCC | 80700 |
| rs764239745 | in-del | -/C | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459779 | ACCCAGGAGGCAGAG[-/C]TTACAGTGAGCCGAG | 80700 |
| rs764273610 | snp | C/T | 5.28975e-05 | 0.00514256 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446188 | AGCCGCTCCCGAGCG[C/T]AGAAAGTGCCTGGGG | 80700 |
| rs764280812 | snp | A/G | 5.14337e-05 | 0.00507092 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452445 | ACAGGTGAAGTACAC[A/G]CCAGGCACAGCCAGG | 80700 |
| rs764291815 | snp | C/T | 3.40194e-05 | 0.00412414 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454026 | CTGCCATCTGTGCCT[C/T]ATTGGTGGGTCCCTG | 80700 |
| rs764371927 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459404 | ATGGGTTGGACGGGT[A/G]GCTCAGGCCTGCAGT | 80700 |
| rs764460254 | in-del | -/TT | 3.60477e-05 | 0.0042453 | frameshift-variant, intron-variant | UBXN6 | GRCh38.p7 | 19:4457626 | GCACCCCACGGACTC[-/TT]TGAGCTTCTGACCGG | 80700 |
| rs764515567 | snp | G/T | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448663 | GCCTTCTCAAGGCTA[G/T]ATCCATGGGACTTGG | 80700 |
| rs764519921 | snp | A/G | 0.000248548 | 0.0111451 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446821 | TCCCTACTCAGCCAG[A/G]CCCTGTCCACTTACC | 80700 |
| rs764525926 | snp | C/T | 8.979e-05 | 0.00669977 | missense | UBXN6 | GRCh38.p7 | 19:4453487 | GGGCCTCGGGGCTCC[C/T]GCTGACGGTGGCTTC | 80700 |
| rs764578977 | snp | A/G | 4.22788e-05 | 0.00459757 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453430 | CCACCCCTTGGCATG[A/G]GACAGTGCCACCAGT | 80700 |
| rs764632030 | snp | A/G | 3.55499e-05 | 0.00421588 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446520 | CCTCTGCTCCCGCTT[A/G]ATCTCCTCTGCTGTG | 80700 |
| rs764656169 | in-del | -/CTC | 6.59881e-05 | 0.00574367 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447589 | GATCTTCCGGTACTT[-/CTC]CTCCTCGGGGTGCAG | 80700 |
| rs764696826 | snp | A/C/G | 6.64975e-05 | 0.00576584 | missense | UBXN6 | GRCh38.p7 | 19:4452396 | TGATGCAGGCGTCCC[A/C/G]CTGGTCCTTCCTCAG | 80700 |
| rs764749887 | snp | C/G | | | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457711 | ATGGTGGCGGCTGGC[C/G]CGGCGGCGGGGGGCC | 80700 |
| rs764795659 | snp | G/T | 1.65102e-05 | 0.00287312 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445565 | GGCTCGGCCCCCGCG[G/T]CCTTGATGTCCTCCA | 80700 |
| rs764813172 | snp | C/T | 7.49578e-05 | 0.00612154 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446182 | GCCCCCAGCCGCTCC[C/T]GAGCGTAGAAAGTGC | 80700 |
| rs764832523 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455841 | TCTCACTGTGTCCTG[A/G]GAGAGGCCTTCCCAA | 80700 |
| rs764844860 | snp | C/T | 9.29109e-05 | 0.00681519 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446400 | GCACGCTCAGCCGCT[C/T]CACCGCCTCGGACCT | 80700 |
| rs764846893 | snp | C/G | 1.6498e-05 | 0.00287206 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445525 | CTCGATGGCTGACAG[C/G]AGCTCGGGTTTCAGG | 80700 |
| rs764917177 | snp | C/T | | | utr-variant-5-prime, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454093 | TTTGTGGGCCTTTTC[C/T]CTGGGAACAGACCGA | 80700 |
| rs764945457 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451295 | ACTTCTGACCTCAGG[G/T]GATCCACCTGCCTCA | 80700 |
| rs765041268 | snp | C/T | | | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446358 | GCCCCCGCTGCTCCT[C/T]CTTCTCCCGCATGGC | 80700 |
| rs765042064 | snp | A/G | | | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446680 | CTCTGGGGCTGGGCC[A/G]AGGTGGTCTCGCTCA | 80700 |
| rs765195277 | snp | C/G | 2.00624e-05 | 0.00316714 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445957 | CCCCTGCTCTGAGAA[C/G]AAGGAGGCTCCCTCC | 80700 |
| rs765248393 | snp | G/T | 1.74583e-05 | 0.00295446 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446541 | CTCTGCTGTGAGGTT[G/T]AAGAAGTCCCCAGGC | 80700 |
| rs765447025 | snp | A/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452615 | CCCATGCTGTCCCTT[A/C]CACCTGGTGGCCGTG | 80700 |
| rs765543803 | in-del | -/C | 2.26742e-05 | 0.00336698 | frameshift-variant, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446167 | CGAACCCGTACACCG[-/C]CCCCCAGCCGCTCCC | 80700 |
| rs765602196 | in-del | ACTCTGTCTC/GGGAGAAAAAAAACCTCTGTCA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450212 | CCTGGTGACAGCAAG[lengthTooLong]AAAAAAAAAAAAAAA | 80700 |
| rs765606534 | in-del | -/A | 1.65908e-05 | 0.00288012 | frameshift-variant, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446881 | GAACCCAATGGCCTC[-/A]AAAAAACTCGTGGGT | 80700 |
| rs765627908 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447841 | CCAGCAGGAGCCCCA[C/T]GGAACCCCTCACCGT | 80700 |
| rs765663855 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459528 | GGGCAACAGAGCCAG[A/G]CCCTGTCTTATTAAA | 80700 |
| rs765691457 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450200 | ACTGCACTCCAGCCT[A/G]GTGACAGCAAGACTC | 80700 |
| rs765781910 | snp | A/C | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459700 | TTAAAAAAATTAGCC[A/C]GCCTTGGTGGCGGGC | 80700 |
| rs765840168 | snp | C/T | 0.000161431 | 0.00898272 | missense | UBXN6 | GRCh38.p7 | 19:4453493 | CGGGGCTCCCGCTGA[C/T]GGTGGCTTCGGCTTG | 80700 |
| rs765845706 | snp | C/T | 1.69928e-05 | 0.00291481 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446723 | CCTCGGGGTCCTCTA[C/T]AGCGTGGCAGGACAT | 80700 |
| rs765887592 | in-del | -/GGGGCCGCGGGGGCGGGGGGGCAC | 0.000354108 | 0.0133014 | cds-indel, intron-variant | UBXN6 | GRCh38.p7 | 19:4457721 | CTGGCCCGGCGGCGG[-/GGGGCCGCGGGGGCGGGGGGGCAC]GGGGCCCAGTCGGGG | 80700 |
| rs765934867 | snp | C/T | 1.78105e-05 | 0.00298412 | missense | UBXN6 | GRCh38.p7 | 19:4452485 | CCTTCCTCTCTGGGC[C/T]CAGATACCTGGGGCG | 80700 |
| rs766077813 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452754 | AGCAGCTTCTGACAC[A/G]CAGGAAACACCCAGC | 80700 |
| rs766184728 | snp | A/G | 8.25621e-05 | 0.0064245 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445573 | CCCCGCGGCCTTGAT[A/G]TCCTCCAGCACAGCC | 80700 |
| rs766203776 | snp | C/T | | | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453467 | TCTTACCACGTTGGT[C/T]CCTGGGGCCTCGGGG | 80700 |
| rs766246007 | snp | A/G/T | 9.77672e-05 | 0.00699113 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448286 | GGGATGAGCTGGAGG[A/G/T]GCCAGGCAGGGCAAA | 80700 |
| rs766341604 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444990 | GTCCCACGGTTTCAA[C/T]GGAGAACCAAGAAAC | 80700 |
| rs766574310 | snp | A/C | 1.70266e-05 | 0.00291771 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446636 | GCACGGGCTCCGCAG[A/C]CAGCAGCTGTTCCTT | 80700 |
| rs766651489 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445032 | AACCTGTTTATTTGG[A/G]CTTATGATTTACTAA | 80700 |
| rs766669347 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447612 | CGGGGTGCAGGTGGA[C/T]GTTGTCCAGGTACCT | 80700 |
| rs766689960 | in-del | -/A | 4.95905e-05 | 0.00497923 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445482 | CACAGGGCTGAGGCC[-/A]AACCCTGCTTTTATT | 80700 |
| rs766893069 | snp | A/G | 1.66098e-05 | 0.00288177 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446885 | CCCAATGGCCTCAAA[A/G]AACTCGTGGGTCCCT | 80700 |
| rs766936200 | snp | C/G | 1.66103e-05 | 0.00288182 | missense | UBXN6 | GRCh38.p7 | 19:4453959 | GTGTCCTGCGATGTG[C/G]GGCCCCAGGCCCGGG | 80700 |
| rs767015341 | snp | A/G | 3.36819e-05 | 0.00410364 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446211 | GCCTGGGGAGTGGGG[A/G]AGTCAGAGCGGGTGG | 80700 |
| rs767239791 | snp | C/G/T | 4.16027e-05 | 0.0045607 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445945 | ACCTGCCCAGGCCCC[C/G/T]TGCTCTGAGAACAAG | 80700 |
| rs767296357 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454645 | TGGTCTCGAACTTTT[A/G]CCTCAAATGATCCTC | 80700 |
| rs767341765 | snp | C/T | 2.1696e-05 | 0.00329356 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453418 | GTCAAGCTGTCCCCA[C/T]CCCTTGGCATGGGAC | 80700 |
| rs767492359 | snp | A/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453534 | CTCACTGGAAGGCAG[A/C]CCAAGAAAGAGAGGC | 80700 |
| rs767543995 | in-del | AGCCTGGGCGACAGAGCGAGACTCTGTCTC/CCCCCGCCGGGGAAAAAAGAGGAAACTTTTTAA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450729 | GCGCCACTGCACTCC[lengthTooLong]AAAAAAAAAAAAAAA | 80700 |
| rs767549651 | snp | C/T | 3.30022e-05 | 0.00406202 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447618 | GCAGGTGGATGTTGT[C/T]CAGGTACCTGGGGTA | 80700 |
| rs767607803 | snp | C/G/T | 0.000254842 | 0.0112853 | missense | UBXN6 | GRCh38.p7 | 19:4454014 | GGGCGGCAGCGGCTG[C/G/T]CATCTGTGCCTCATT | 80700 |
| rs767747500 | snp | A/C/T | 3.59074e-05 | 0.00423706 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452490 | CTCTCTGGGCTCAGA[A/C/T]ACCTGGGGCGGTGAA | 80700 |
| rs767847248 | snp | A/G | 9.64795e-05 | 0.00694481 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446154 | CAGGGCCTCCCGGAC[A/G]AACCCGTACACCGCC | 80700 |
| rs767870865 | snp | A/C | 3.33028e-05 | 0.00408048 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446457 | TGGCCGGGGTTCTTC[A/C]ACCCCGCCCCGCCCC | 80700 |
| rs767897891 | snp | G/T | 0.000152213 | 0.00872259 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446100 | GGACAGCTTCTGCCC[G/T]CCCGAGGCCAGCAGC | 80700 |
| rs768019361 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451117 | GCTGGAGCTCAATGG[C/T]GTGATCTGGGCTCAC | 80700 |
| rs768028773 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455940 | GCGCTCATCCAAGGT[C/G]TGTTGGTTTATTTGT | 80700 |
| rs768067182 | snp | C/T | 1.65578e-05 | 0.00287726 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447673 | GCCCAGGCTGCCCAC[C/T]CGGCCCCTCTGTGCC | 80700 |
| rs768128760 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450454 | TAGGCAAAAGCCTAA[A/G]TTGCCTAATATGTAA | 80700 |
| rs768286506 | snp | A/G | 3.32801e-05 | 0.00407908 | stop-gained | UBXN6 | GRCh38.p7 | 19:4453939 | TCTCACCCTGGTTTC[A/G]GATGGTGTCCTGCGA | 80700 |
| rs768454692 | in-del | -/CCACC | 3.36095e-05 | 0.00409922 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446455 | CTGGCCGGGGTTCTT[-/CCACC]CCACCCCGCCCCGCC | 80700 |
| rs768462696 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456822 | GCGTCTGTCTCACCC[A/G]TCTTCTCCTCTCAGG | 80700 |
| rs768690108 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447411 | CTACCTTCTACTGGC[C/T]GAACCCTTCACTGCT | 80700 |
| rs768797793 | snp | C/T | 1.75752e-05 | 0.00296433 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454064 | GGCCTGGGGGCTGGC[C/T]GGTTGGGCTTCTCTT | 80700 |
| rs768800563 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451159 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 80700 |
| rs768817535 | snp | C/G | 1.82091e-05 | 0.00301732 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454138 | ATCCTCCCGAGGTGG[C/G]CGGCAAAGCTGACGT | 80700 |
| rs768918852 | snp | A/C | 1.67094e-05 | 0.0028904 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446253 | CCCTACCAACCCGAG[A/C]CGCCCTCCACGGGCA | 80700 |
| rs768962882 | snp | A/T | 1.65625e-05 | 0.00287766 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445985 | TCCTGGGGGTGTCTG[A/T]GCCGGTCCCAGGAGA | 80700 |
| rs769037800 | snp | A/C | 1.72282e-05 | 0.00293492 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446586 | GGCCAGGGGCGAGGG[A/C]TGGAAGACGCGGCGC | 80700 |
| rs769069644 | snp | A/T | 3.36814e-05 | 0.0041036 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452324 | GGCTCAGGCACAGGA[A/T]GCTACAGGTTGGGGC | 80700 |
| rs769074676 | snp | A/G | 1.6563e-05 | 0.00287771 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445459 | AACAGGGAGAGCATG[A/G]GACAGACCCACAGGG | 80700 |
| rs769092781 | snp | C/G | 0.000289402 | 0.0120257 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448423 | GAGAAGTGCTGGGAG[C/G]AGGGAAGCAGGGAAA | 80700 |
| rs769207843 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444826 | ACAGCCTCCCCTAGC[A/G]CACGGGACTTCCTCC | 80700 |
| rs769400511 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451694 | CCAGGTTGGAGTGCA[A/G]TGGCGCTATCTCGGC | 80700 |
| rs769467769 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455556 | GCGTCAGCATCACTC[C/G]ACTGCACAACGCCCT | 80700 |
| rs769537202 | snp | C/T | 1.89288e-05 | 0.00307637 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453458 | AGTGGCTGTTCTTAC[C/T]ACGTTGGTCCCTGGG | 80700 |
| rs769538645 | snp | C/G | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448562 | ACAGAAAGGAAAAGA[C/G]AGACCCTCCAAGACC | 80700 |
| rs769769112 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458224 | GGCAACATGGCAAAA[-/C]CTCGTCTCTATAAAA | 80700 |
| rs769802228 | snp | A/G | | | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447554 | GGCACGCCCACCTGA[A/G]ACACCTTGTTCTGCA | 80700 |
| rs769896307 | snp | C/T | 6.63669e-05 | 0.00576013 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445627 | GGCAGAGGGCACCTG[C/T]GGTAGGGGTAGGCCG | 80700 |
| rs769933433 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454165 | ACGTGCAGTCACACA[C/G]AGGAGCTTCTGCCCC | 80700 |
| rs770045495 | snp | G/T | 1.65482e-05 | 0.00287643 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445472 | TGAGACAGACCCACA[G/T]GGCTGAGGCCAACCC | 80700 |
| rs770045889 | snp | C/G | 1.66643e-05 | 0.0028865 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446322 | GGCGCACGCGCAGCA[C/G]CGTGTAGTTGTACTT | 80700 |
| rs770061432 | in-del | -/AG | 5.67306e-05 | 0.00532561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453542 | AAGGCAGCCCAAGAA[-/AG]AGAGGCAGAGACGGG | 80700 |
| rs770141698 | snp | A/C/T | 3.76877e-05 | 0.00434082 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446149 | CTCTGCAGGGCCTCC[A/C/T]GGACGAACCCGTACA | 80700 |
| rs770163788 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4455153 | CCTCGCAGAGAAGCC[C/G]TTTCTCCCAACCTGC | 80700 |
| rs770164345 | snp | C/G | 1.66189e-05 | 0.00288256 | missense | UBXN6 | GRCh38.p7 | 19:4453951 | TTCGGATGGTGTCCT[C/G]CGATGTGGGGCCCCA | 80700 |
| rs770255930 | snp | C/T | 0.000204757 | 0.0101162 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446630 | TGGCGCGCACGGGCT[C/T]CGCAGCCAGCAGCTG | 80700 |
| rs770274831 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451555 | GACAGGGTTTTGCCA[C/T]GTTGCCCAGGCTAAA | 80700 |
| rs770469568 | snp | A/G | 3.36978e-05 | 0.0041046 | missense | UBXN6 | GRCh38.p7 | 19:4452428 | GTGGCCCCAGTGAGC[A/G]GACAGGTGAAGTACA | 80700 |
| rs770506195 | snp | A/C | 2.11312e-05 | 0.0032504 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445936 | AACCCAGGGACCTGC[A/C]CAGGCCCCCTGCTCT | 80700 |
| rs770615062 | snp | A/G/T | 6.62784e-05 | 0.00575635 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448314 | AAAGGGGCCACACGC[A/G/T]CACTTGGCAATGGTG | 80700 |
| rs770632078 | snp | A/G/T | 3.67608e-05 | 0.00428711 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453526 | GTTCCTTTCTCACTG[A/G/T]AAGGCAGCCCAAGAA | 80700 |
| rs770668194 | snp | A/G | 1.66724e-05 | 0.0028872 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446264 | CGAGCCGCCCTCCAC[A/G]GGCATCGTTGGTGCC | 80700 |
| rs770668271 | snp | A/G | 1.95854e-05 | 0.00312927 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446949 | TGGGCGTCACTGGGG[A/G]CCCCTGGCTTCCTCC | 80700 |
| rs770829188 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449354 | CACCCCCCACCCTCA[A/G]CTGCACAGCAGGGTC | 80700 |
| rs770930389 | in-del | -/CAAT | 0.000136022 | 0.00824576 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446752 | ATGGGTGTCACTGTG[-/CAAT]GGAGAGACCCCCAAG | 80700 |
| rs770966797 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455409 | GATGACTCATGAAGA[C/T]CCACCCCGGCCTCAT | 80700 |
| rs771004329 | in-del | -/T | 0.000194479 | 0.00985909 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453422 | AGCTGTCCCCACCCC[-/T]TGGCATGGGACAGTG | 80700 |
| rs771033377 | snp | C/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447869 | CGTCCCACCAGCCCT[C/G]GAAGGGCACAATTAA | 80700 |
| rs771051443 | snp | G/T | 1.69304e-05 | 0.00290945 | missense | UBXN6 | GRCh38.p7 | 19:4452435 | CAGTGAGCGGACAGG[G/T]GAAGTACACGCCAGG | 80700 |
| rs771112261 | snp | G/T | 3.34219e-05 | 0.00408777 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452353 | GCAGGAGCACACAGG[G/T]TGCCACTCACCAAGA | 80700 |
| rs771290724 | snp | A/G | 3.31049e-05 | 0.00406834 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447667 | GGCACAGCCCAGGCT[A/G]CCCACCCGGCCCCTC | 80700 |
| rs771539681 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449418 | ACCTACACACTGAGC[C/T]GGGGCTCATGCCAAC | 80700 |
| rs771603858 | snp | A/G | 8.50796e-05 | 0.0065217 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446758 | GTCACTGTGCAATGG[A/G]GAGACCCCCAAGCCG | 80700 |
| rs771671346 | snp | A/G | 1.86548e-05 | 0.00305402 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453532 | TTCTCACTGGAAGGC[A/G]GCCCAAGAAAGAGAG | 80700 |
| rs771703000 | snp | A/G | 9.68242e-05 | 0.00695721 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446389 | CTTGGTCCGCAGCAC[A/G]CTCAGCCGCTCCACC | 80700 |
| rs771729797 | snp | G/T | 3.63478e-05 | 0.00426293 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457668 | CTTGAACTTGATGTC[G/T]GCCTTGAACTCCTGA | 80700 |
| rs771796401 | snp | A/G | 1.65405e-05 | 0.00287576 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445477 | CAGACCCACAGGGCT[A/G]AGGCCAACCCTGCTT | 80700 |
| rs771805982 | in-del | -/TGCCA | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445333 | AAGGGATGGGGGCTC[-/TGCCA]CGGGGCCCAATTCCA | 80700 |
| rs771869942 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455541 | AACCTCAGCCAGGGA[C/G]CGTCAGCATCACTCC | 80700 |
| rs771897085 | snp | A/G | 1.64982e-05 | 0.00287208 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447582 | GCAGCTTGATCTTCC[A/G]GTACTTCTCCTCCTC | 80700 |
| rs771996432 | in-del | -/CCTC | 3.32978e-05 | 0.00408017 | frameshift-variant | UBXN6 | GRCh38.p7 | 19:4452406 | GTCCCGCTGGTCCTT[-/CCTC]AGGGTGGCCCCAGTG | 80700 |
| rs772092117 | snp | C/T | 0.000116099 | 0.00761813 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447513 | CCAGCTGCCCCCACC[C/T]CCAGCCTGGGCCCCG | 80700 |
| rs772192657 | in-del | -/CCTCTGCTCCCGCTTGATCT | 1.87023e-05 | 0.0030579 | frameshift-variant, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446504 | TCAGGCCCACCTGAG[-/CCTCTGCTCCCGCTTGATCT]CCTCTGCTCCCGCTT | 80700 |
| rs772230469 | snp | C/T | 1.68975e-05 | 0.00290662 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446701 | GTCTCGCTCAGCACG[C/T]AGAACTCCTCGGGGT | 80700 |
| rs772240209 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456638 | CCCCGGCCCTCCCAG[C/T]TGGCTCAGCCCTGCT | 80700 |
| rs772242326 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445864 | GGAAACTGAGGCGTG[A/G]AGTAGTTATGAACTT | 80700 |
| rs772295747 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451848 | GCAAATAATACTTAA[C/T]CTTTTATGAAAAACA | 80700 |
| rs772332941 | snp | C/G | 1.6638e-05 | 0.00288422 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446785 | GCCGGGCCCTCCTGC[C/G]CCGAGGCCCCTCGTC | 80700 |
| rs772380278 | snp | A/C/G | 5.18581e-05 | 0.00509185 | synonymous-codon, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448404 | GGCGGCCACTGGGTC[A/C/G]GTGGAGAAGTGCTGG | 80700 |
| rs772387266 | snp | C/G/T | 4.12916e-05 | 0.00454358 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452512 | GGCGGTGAAAGCGTC[C/G/T]AAGTCTGGACCGTGG | 80700 |
| rs772543313 | snp | A/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453172 | CCGGTTCTCTTTTTG[A/C]ATAGTGGAAACTGTA | 80700 |
| rs772734967 | snp | C/G | 9.22126e-05 | 0.00678954 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446248 | GGGCCCCCTACCAAC[C/G]CGAGCCGCCCTCCAC | 80700 |
| rs772866029 | snp | A/G | 1.65381e-05 | 0.00287555 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447663 | GTGGGGCACAGCCCA[A/G]GCTGCCCACCCGGCC | 80700 |
| rs772883974 | snp | C/T | 3.75594e-05 | 0.00433339 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446441 | GCCAGGTCACGAGGG[C/T]TGGCCGGGGTTCTTC | 80700 |
| rs772943511 | snp | A/G | 4.65755e-05 | 0.00482552 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446402 | ACGCTCAGCCGCTCC[A/G]CCGCCTCGGACCTGC | 80700 |
| rs773031256 | snp | C/T | 1.66167e-05 | 0.00288237 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446794 | TCCTGCCCCGAGGCC[C/T]CTCGTCCCCATTCCC | 80700 |
| rs773084247 | snp | A/C | 9.25069e-05 | 0.00680036 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452537 | CCGTGGACAGAGGCC[A/C]CCCCGACCCTCGCCG | 80700 |
| rs773351095 | snp | G/T | 2.11867e-05 | 0.00325467 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445933 | TCAAACCCAGGGACC[G/T]GCCCAGGCCCCCTGC | 80700 |
| rs773452969 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444948 | GCCCCCAAGCCATCC[A/G]CTCTTCAGCAGGTGG | 80700 |
| rs773471756 | snp | A/G | 6.60677e-05 | 0.00574713 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447646 | GTAGGTGGAGAAGGT[A/G]AGTGGGGCACAGCCC | 80700 |
| rs773496682 | snp | C/T | 4.98509e-05 | 0.00499229 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453952 | TCGGATGGTGTCCTG[C/T]GATGTGGGGCCCCAG | 80700 |
| rs773698248 | in-del | C/TGAGATTGCACCA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450173 | GAGGTTGCAGTGAGC[C/TGAGATTGCACCA]CTGCACTCCAGCCTG | 80700 |
| rs773705654 | snp | C/T | 3.38782e-05 | 0.00411557 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446077 | TTCAAGGCCAGGTTC[C/T]CGTCCTCGGACAGCT | 80700 |
| rs773725600 | snp | G/T | 3.73434e-05 | 0.00432091 | missense | UBXN6 | GRCh38.p7 | 19:4453462 | GCTGTTCTTACCACG[G/T]TGGTCCCTGGGGCCT | 80700 |
| rs773811236 | snp | C/G/T | 5.01461e-05 | 0.00500709 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445655 | CCGTCACTCTGAGAC[C/G/T]GAGAGTCGGCCCTTG | 80700 |
| rs773932661 | snp | A/G | 2.10813e-05 | 0.00324657 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445940 | CAGGGACCTGCCCAG[A/G]CCCCCTGCTCTGAGA | 80700 |
| rs773959023 | snp | C/T | 2.19986e-05 | 0.00331644 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453409 | CGTGACACAGTCAAG[C/T]TGTCCCCACCCCTTG | 80700 |
| rs774101724 | snp | A/G | 1.65754e-05 | 0.00287879 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446877 | TTCTGGAACCCAATG[A/G]CCTCAAAAAACTCGT | 80700 |
| rs774106518 | snp | C/T | 0.000154206 | 0.00877948 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446323 | GCGCACGCGCAGCAG[C/T]GTGTAGTTGTACTTG | 80700 |
| rs774165477 | snp | C/T | 0.000145904 | 0.00853994 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446270 | GCCCTCCACGGGCAT[C/T]GTTGGTGCCCACCCT | 80700 |
| rs774229362 | snp | C/T | 2.08041e-05 | 0.00322515 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446960 | GGGGGCCCCTGGCTT[C/T]CTCCATGGCCTGGCC | 80700 |
| rs774325900 | in-del | -/CCCCG | 0.000102196 | 0.00714754 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446458 | GCCGGGGTTCTTCCA[-/CCCCG]CCCCGCCCCGCCCCA | 80700 |
| rs774347058 | snp | G/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447958 | CAGTGCCAGCAGGGG[G/T]CTCCTGCGGGGTGCT | 80700 |
| rs774381742 | snp | A/G | 1.69479e-05 | 0.00291095 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452436 | AGTGAGCGGACAGGT[A/G]AAGTACACGCCAGGC | 80700 |
| rs774534985 | snp | A/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454496 | GGCACGATCATGGCT[A/T]ACTGCAATCCTGAGC | 80700 |
| rs774546745 | snp | A/G | 1.92417e-05 | 0.00310169 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446152 | TGCAGGGCCTCCCGG[A/G]CGAACCCGTACACCG | 80700 |
| rs774623043 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455420 | AAGACCCACCCCGGC[A/C]TCATCCGATATCTGG | 80700 |
| rs774653205 | snp | C/T | 1.69674e-05 | 0.00291263 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446649 | AGCCAGCAGCTGTTC[C/T]TTGTGCCTCTCCAGG | 80700 |
| rs774703108 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444991 | TCCCACGGTTTCAAC[A/G]GAGAACCAAGAAACT | 80700 |
| rs774741632 | snp | C/T | 1.65559e-05 | 0.00287709 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447670 | ACAGCCCAGGCTGCC[C/T]ACCCGGCCCCTCTGT | 80700 |
| rs774841586 | snp | C/G | 3.32049e-05 | 0.00407448 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453970 | TGTGGGGCCCCAGGC[C/G]CGGGACTGCTTCTGC | 80700 |
| rs774846820 | snp | C/G | 1.6582e-05 | 0.00287936 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447514 | CAGCTGCCCCCACCC[C/G]CAGCCTGGGCCCCGG | 80700 |
| rs775101855 | snp | C/T | 1.66247e-05 | 0.00288307 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446888 | AATGGCCTCAAAAAA[C/T]TCGTGGGTCCCTTCC | 80700 |
| rs775189130 | snp | C/T | 1.92022e-05 | 0.0030985 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445983 | CCTCCTGGGGGTGTC[C/T]GTGCCGGTCCCAGGA | 80700 |
| rs775197295 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455745 | GAATGTTCTCCGGGG[C/G]AGTGGGAGGAGGATG | 80700 |
| rs775220787 | snp | C/T | 5.42373e-05 | 0.00520727 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446344 | GTTGTACTTGCGCAG[C/T]CCCCGCTGCTCCTCC | 80700 |
| rs775280456 | in-del | -/AA | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458867 | CGAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 80700 |
| rs775285745 | snp | A/C | 1.65072e-05 | 0.00287286 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445495 | GCCAACCCTGCTTTT[A/C]TTTCACAAGAGCTTC | 80700 |
| rs775376208 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456657 | CTCAGCCCTGCTCAG[A/G]CCCTTCTCTCCAAGT | 80700 |
| rs775376246 | snp | C/T | 0.000143106 | 0.00845769 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446392 | GGTCCGCAGCACGCT[C/T]AGCCGCTCCACCGCC | 80700 |
| rs775540964 | snp | C/T | 1.65699e-05 | 0.00287831 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447674 | CCCAGGCTGCCCACC[C/T]GGCCCCTCTGTGCCT | 80700 |
| rs775635838 | snp | A/G | 3.48997e-05 | 0.00417716 | utr-variant-5-prime, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454057 | GCGGGGCGGCCTGGG[A/G]GCTGGCTGGTTGGGC | 80700 |
| rs775656886 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453224 | TTAAGGGGAGGGAGC[A/G]ATGGGCTCGTGTACC | 80700 |
| rs775713602 | snp | A/C/T | 0.000305327 | 0.0123523 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446159 | CCTCCCGGACGAACC[A/C/T]GTACACCGCCCCCAG | 80700 |
| rs775807120 | snp | A/G | 3.45101e-05 | 0.00415378 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446581 | TGCGAGGCCAGGGGC[A/G]AGGGCTGGAAGACGC | 80700 |
| rs775831354 | in-del | -/CTT | 4.98074e-05 | 0.00499011 | cds-indel | UBXN6 | GRCh38.p7 | 19:4453979 | CCAGGCCCGGGACTG[-/CTT]CTGCTCCAGCCGGGC | 80700 |
| rs776229378 | snp | A/C/G/T | 0.000152332 | 0.00872624 | missense, synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446664 | CTTGTGCCTCTCCAG[A/C/G/T]CTCTGGGGCTGGGCC | 80700 |
| rs776252821 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455426 | CACCCCGGCCTCATC[C/T]GATATCTGGGTCTTT | 80700 |
| rs776268944 | snp | A/G | 9.42285e-05 | 0.00686334 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446397 | GCAGCACGCTCAGCC[A/G]CTCCACCGCCTCGGA | 80700 |
| rs776335321 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450652 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 80700 |
| rs776364037 | snp | C/T | 1.65448e-05 | 0.00287613 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447527 | CCCCAGCCTGGGCCC[C/T]GGGGGCCAGAAGGCA | 80700 |
| rs776367673 | snp | C/T | 1.65089e-05 | 0.00287301 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445563 | CCGGCTCGGCCCCCG[C/T]GGCCTTGATGTCCTC | 80700 |
| rs776470883 | snp | C/T | 1.69344e-05 | 0.00290979 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446706 | GCTCAGCACGTAGAA[C/T]TCCTCGGGGTCCTCT | 80700 |
| rs776516740 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447436 | ACTGCTTGTGGCTCA[A/G]CTCTCGCTAGCTCCT | 80700 |
| rs776558429 | snp | C/G | 1.69052e-05 | 0.00290728 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457699 | AAGAATTTCTTCATG[C/G]TGGCGGCTGGCCCGG | 80700 |
| rs776608642 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455824 | ATTTCCCCACAGCTG[A/C]GTCTCACTGTGTCCT | 80700 |
| rs776614212 | snp | A/G | 5.15637e-05 | 0.00507732 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448339 | ATGGTGTCCACACCC[A/G]GCTTCACCCGGTCCT | 80700 |
| rs776616233 | in-del | -/C | 1.80592e-05 | 0.00300487 | frameshift-variant | UBXN6 | GRCh38.p7 | 19:4453514 | CTTCGGCTTGAAGTT[-/C]CTTTCTCACTGGAAG | 80700 |
| rs776651024 | snp | A/G | 9.63159e-05 | 0.00693893 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446255 | CTACCAACCCGAGCC[A/G]CCCTCCACGGGCATC | 80700 |
| rs776766795 | snp | A/G | 2.99927e-05 | 0.00387239 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448425 | GAAGTGCTGGGAGGA[A/G]GGAAGCAGGGAAAGC | 80700 |
| rs776855886 | snp | A/G | 1.95804e-05 | 0.00312887 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453557 | AGAGAGGCAGAGACG[A/G]GATAGTGAGCACGCC | 80700 |
| rs776865157 | in-del | -/GA | 3.40159e-05 | 0.00412393 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446757 | TGTCACTGTGCAATG[-/GA]GAGACCCCCAAGCCG | 80700 |
| rs777010232 | in-del | -/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451314 | CACCTGCCTCAGCCT[-/C]CCCAAAGCACTGGAA | 80700 |
| rs777012898 | snp | C/T | 1.91086e-05 | 0.00309094 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445988 | TGGGGGTGTCTGTGC[C/T]GGTCCCAGGAGAACC | 80700 |
| rs777127794 | snp | C/T | 0.000147525 | 0.00858725 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446488 | ACTCTGCTCCGCGGA[C/T]GTCAGGCCCACCTGA | 80700 |
| rs777136034 | snp | A/G | 1.66269e-05 | 0.00288326 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453943 | ACCCTGGTTTCGGAT[A/G]GTGTCCTGCGATGTG | 80700 |
| rs777138995 | snp | A/G | 1.72181e-05 | 0.00293407 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446589 | CAGGGGCGAGGGCTG[A/G]AAGACGCGGCGCTGC | 80700 |
| rs777270364 | snp | A/G | 0.000227661 | 0.0106667 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444629 | GGACCACCCAGGATC[A/G]TCTCCCAGCTCAAGA | 80700 |
| rs777292954 | snp | A/G/T | 3.634e-05 | 0.0042625 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454119 | ACCGAGGGAGAGTGA[A/G/T]TGTATCCTCCCGAGG | 80700 |
| rs777310844 | snp | A/C | 2.38912e-05 | 0.00345615 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448377 | GTTGAACGTGTAGAT[A/C]TTCATGATGGAGGCG | 80700 |
| rs777524168 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453079 | GGACAGGCTCTGAAA[C/T]CACAGACTGGCTCTG | 80700 |
| rs777527497 | snp | C/T | 1.79958e-05 | 0.0029996 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453506 | GACGGTGGCTTCGGC[C/T]TGAAGTTCCTTTCTC | 80700 |
| rs777582814 | snp | C/T | 7.52092e-05 | 0.0061318 | missense | UBXN6 | GRCh38.p7 | 19:4453460 | TGGCTGTTCTTACCA[C/T]GTTGGTCCCTGGGGC | 80700 |
| rs777597792 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450574 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 80700 |
| rs777668045 | snp | C/T | 5.51405e-05 | 0.00525045 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446023 | GAGGCATCGGGTCAG[C/T]GGTGCTCCTGCGGGC | 80700 |
| rs777727034 | snp | A/G | 3.88086e-05 | 0.00440486 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445974 | AGGAGGCTCCCTCCT[A/G]GGGGTGTCTGTGCCG | 80700 |
| rs777741750 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449271 | GAGGGCGGGTGAACA[G/T]AAGGGCAGCCCAGGG | 80700 |
| rs777794811 | in-del | -/G | 1.77084e-05 | 0.00297554 | frameshift-variant | UBXN6 | GRCh38.p7 | 19:4452481 | AGAGCCTTCCTCTCT[-/G]GGCTCAGATACCTGG | 80700 |
| rs777860200 | in-del | -/GGAA | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447784 | AGACCATCTCCGGGT[-/GGAA]GGCACACCTCGGACA | 80700 |
| rs777934244 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4455171 | TCTCCCAACCTGCTC[A/G]GACGCGTCTGTCTCA | 80700 |
| rs777946490 | snp | A/G | 0.000404514 | 0.014216 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457737 | GGGCCGCGGGGGCGG[A/G]GGGGCACGGGGCCCA | 80700 |
| rs777982873 | snp | C/T | 1.68675e-05 | 0.00290405 | missense | UBXN6 | GRCh38.p7 | 19:4452431 | GCCCCAGTGAGCGGA[C/T]AGGTGAAGTACACGC | 80700 |
| rs778155355 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456770 | GACGTGGCAGAGAAG[C/G]CTCGCAGAGAAGCTC | 80700 |
| rs778183237 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456098 | AGGGACCTCCGCACC[A/G]CTTCCTTTCCCAACC | 80700 |
| rs778247312 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454730 | CCGCATCCTCAGGAA[C/T]TGAGGAGACTCAAGG | 80700 |
| rs778305826 | snp | C/G | 1.72803e-05 | 0.00293936 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446578 | AACTGCGAGGCCAGG[C/G]GCGAGGGCTGGAAGA | 80700 |
| rs778453571 | snp | C/T | 1.71664e-05 | 0.00292966 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446602 | TGGAAGACGCGGCGC[C/T]GCCTGTCCAGCTTGG | 80700 |
| rs778473018 | snp | A/G | 2.5162e-05 | 0.00354688 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448396 | ATGATGGAGGCGGCC[A/G]CTGGGTCGGTGGAGA | 80700 |
| rs778477290 | snp | C/T | 0.000222544 | 0.0105462 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444640 | GATCATCTCCCAGCT[C/T]AAGACCTTTCATCAT | 80700 |
| rs778670419 | in-del | -/TA | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445006 | GGAGAACCAAGAAAC[-/TA]TATTCAAACAACCTG | 80700 |
| rs778836046 | in-del | -/CCTCCTTGATGCAGGCGTCCCGCTGGT/GC | 1.6609e-05 | 0.0028817 | cds-indel, frameshift-variant | UBXN6 | GRCh38.p7 | 19:4452374 | TCACCAAGAGAATGG[lengthTooLong]CCTCCTTGATGCAGG | 80700 |
| rs778836072 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450144 | GCAGGTGAATTGCTT[C/G]AACCCGGGAAGCAGA | 80700 |
| rs778837233 | snp | G/T | 2.0595e-05 | 0.0032089 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453437 | TTGGCATGGGACAGT[G/T]CCACCAGTGGCTGTT | 80700 |
| rs778966561 | snp | C/T | 1.81069e-05 | 0.00300884 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446034 | TCAGCGGTGCTCCTG[C/T]GGGCCGACACTCACC | 80700 |
| rs779032404 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449387 | TCAGCAGCCCCCTGC[A/G]TCACACGGACCAATG | 80700 |
| rs779057180 | in-del | -/A | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458453 | GTCTCCCCAGAGCTT[-/A]ACGTGATAAAATCCC | 80700 |
| rs779059765 | snp | C/T | 1.65266e-05 | 0.00287455 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445590 | CCTCCAGCACAGCCA[C/T]GTCCCACGAGAAGGT | 80700 |
| rs779083165 | snp | C/T | 2.03511e-05 | 0.00318985 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452508 | CTGGGGCGGTGAAAG[C/T]GTCCAAGTCTGGACC | 80700 |
| rs779110246 | snp | A/G | 0.000102112 | 0.00714462 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446761 | ACTGTGCAATGGAGA[A/G]ACCCCCAAGCCGGGC | 80700 |
| rs779239919 | snp | C/T | 1.82777e-05 | 0.003023 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454128 | GAGTGAGTGTATCCT[C/T]CCGAGGTGGCCGGCA | 80700 |
| rs779379763 | snp | C/G | 4.8308e-05 | 0.00491444 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446290 | GTGCCCACCCTGCAG[C/G]AGGCAGCCATCGGGG | 80700 |
| rs779457601 | in-del | -/CCACACGCTCACTTGGCAATGGTGT | 3.87499e-05 | 0.00440153 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448306 | GGCAGGGCAAAGGGG[-/CCACACGCTCACTTGGCAATGGTGT]CCACACCCAGCTTCA | 80700 |
| rs779480872 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457224 | CATGATCCCGTTTTT[C/T]CCCAAAGGTCGTTCC | 80700 |
| rs779496451 | snp | C/T | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447070 | TGCCTCAGTGCTGGA[C/T]GCAAACCTGCTTTTC | 80700 |
| rs779506389 | snp | A/G | 1.6713e-05 | 0.00289072 | missense | UBXN6 | GRCh38.p7 | 19:4452413 | TGGTCCTTCCTCAGG[A/G]TGGCCCCAGTGAGCG | 80700 |
| rs779509236 | snp | C/T | 1.69683e-05 | 0.00291271 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446115 | TCCCGAGGCCAGCAG[C/T]TCAAAAGGCAGCCAG | 80700 |
| rs779694784 | in-del | -/AAGA | 3.68507e-05 | 0.00429232 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446444 | GGTCACGAGGGCTGG[-/AAGA]CCGGGGTTCTTCCAC | 80700 |
| rs780077096 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452989 | GCCCACCTCCTAGAG[A/G]AAGGCCTCCCTGATT | 80700 |
| rs780110004 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447995 | GCGTTGGCGGGCAGC[A/G]TGGACCTCCAGGCCT | 80700 |
| rs780138602 | snp | C/G | 5.37225e-05 | 0.00518251 | missense | UBXN6 | GRCh38.p7 | 19:4453495 | GGGCTCCCGCTGACG[C/G]TGGCTTCGGCTTGAA | 80700 |
| rs780161784 | snp | C/T | 0.000185675 | 0.00963344 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446249 | GGCCCCCTACCAACC[C/T]GAGCCGCCCTCCACG | 80700 |
| rs780330722 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451184 | GCCTCAGTCTCCTGA[A/G]TAGCTGGGATTACAG | 80700 |
| rs780367624 | snp | A/G | 1.82247e-05 | 0.00301861 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454133 | AGTGTATCCTCCCGA[A/G]GTGGCCGGCAAAGCT | 80700 |
| rs780382263 | snp | C/T | 1.95835e-05 | 0.00312911 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445967 | GAGAACAAGGAGGCT[C/T]CCTCCTGGGGGTGTC | 80700 |
| rs780500807 | snp | C/G | 1.78535e-05 | 0.00298771 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457629 | CCCCACGGACTCTTT[C/G]AGCTTCTGACCGGGT | 80700 |
| rs780583507 | snp | A/G | 1.65658e-05 | 0.00287795 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445452 | GGAGAGGAACAGGGA[A/G]AGCATGAGACAGACC | 80700 |
| rs780595977 | snp | A/G | 0.000209574 | 0.0102344 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454058 | CGGGGCGGCCTGGGG[A/G]CTGGCTGGTTGGGCT | 80700 |
| rs780606829 | snp | A/G | 1.66418e-05 | 0.00288455 | missense | UBXN6 | GRCh38.p7 | 19:4453993 | GCTTCTGCTCCAGCC[A/G]GGCTAGGGCGGCAGC | 80700 |
| rs780660876 | in-del | -/CTT | 0.000315217 | 0.0125503 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446359 | CCCCCGCTGCTCCTC[-/CTT]CTCCCGCATGGCCTT | 80700 |
| rs780697668 | snp | A/G | 2.24853e-05 | 0.00335293 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446173 | CCGTACACCGCCCCC[A/G]GCCGCTCCCGAGCGT | 80700 |
| rs780738119 | snp | G/T | 3.42436e-05 | 0.00413771 | utr-variant-5-prime, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454036 | TGCCTCATTGGTGGG[G/T]CCCTGGCGGGGCGGC | 80700 |
| rs780823252 | snp | A/C/G/T | 0.000118216 | 0.00768747 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445675 | GTCGGCCCTTGCCGC[A/C/G/T]GCAGGGAACTCAGCG | 80700 |
| rs780979396 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458966 | CCAGTTAATAGTGGC[A/G]TACTTTGGTCTGTGC | 80700 |
| rs781063726 | in-del | -/CTC | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456827 | TGTCTCACCCGTCTT[-/CTC]CTCTCAGGCCCCTCC | 80700 |
| rs781209925 | snp | A/G | | | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448305 | AGGCAGGGCAAAGGG[A/G]CCACACGCTCACTTG | 80700 |
| rs781219649 | snp | A/C | 1.66849e-05 | 0.00288828 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446381 | CGCATGGCCTTGGTC[A/C]GCAGCACGCTCAGCC | 80700 |
| rs781312851 | snp | C/T | 0.000123703 | 0.00786359 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448348 | ACACCCAGCTTCACC[C/T]GGTCCTGGTCTTTGT | 80700 |
| rs781397696 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454457 | AGACAGGGTCTTGCT[C/G]TCTCACCAAGGCTGG | 80700 |
| rs781404101 | snp | A/C/T | 3.41054e-05 | 0.00412938 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453896 | GAGAACCTCAAACAG[A/C/T]CCCAACCTGGGCCCG | 80700 |
| rs781417516 | snp | C/T | 8.8476e-05 | 0.00665058 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457645 | AGCTTCTGACCGGGT[C/T]CCGCGCTCTTGAACT | 80700 |
| rs781601968 | snp | A/C | 1.68997e-05 | 0.00290682 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446681 | TCTGGGGCTGGGCCA[A/C]GGTGGTCTCGCTCAG | 80700 |
| rs781621616 | snp | A/C/G | 3.304e-05 | 0.00406437 | missense, synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445581 | CCTTGATGTCCTCCA[A/C/G]CACAGCCATGTCCCA | 80700 |
| rs781642785 | snp | C/T | 1.67581e-05 | 0.00289461 | missense | UBXN6 | GRCh38.p7 | 19:4452417 | CCTTCCTCAGGGTGG[C/T]CCCAGTGAGCGGACA | 80700 |
| rs781741467 | snp | A/G | 0.000202286 | 0.0100549 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457730 | CGGCGGGGGGCCGCG[A/G]GGGCGGGGGGGCACG | 80700 |
| rs796229496 | snp | A/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452677 | GAGTCTTTTCCCTGG[A/T]ATGTCAAATGTCCCT | 80700 |
| rs796466618 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456804 | CTCCCAGCCTGCTAA[G/T]ACGCGTCTGTCTCAC | 80700 |
| rs796777221 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455807 | GAGAGAAGGAGGGGC[A/G]GATTTCCCCACAGCT | 80700 |
| rs796834823 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456475 | TACAGACCCGTGTCC[A/T]GGCTGCCTGGCTGAC | 80700 |
| rs796996547 | in-del | -/GC | | | frameshift-variant | UBXN6 | GRCh38.p7 | 19:4452374 | CTCACCAAGAGAATG[-/GC]CTCCTTGATGCAGGC | 80700 |