SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3212 | snp | C/T | 0.364817 | 0.222075 | intron-variant, utr-variant-3-prime, downstream-variant-500B | USP19 | GRCh38.p7 | 3:49108308 | CCCCTCAGCTTCCCA[C/T]TGACAGAGCCAGTGT | 10869 |
rs14644 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | USP19 | GRCh38.p7 | 3:49108181 | AGAATTGAAGGTACA[A/T]CAGAATCAAATCACG | 10869 |
rs2301373 | snp | A/T | 0.000263622 | 0.0114779 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49122657 | TTGTCCCCTTTGGCA[A/T]CTCCCGGTGTCTGTA | 10869 |
rs3192123 | snp | A/G | 0 | 0 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49121475 | CGGGATGAGGCTCGG[A/G]ACCTGTTGCAAGCCG | 10869 |
rs3209614 | snp | C/T | 1.66192e-05 | 0.00288259 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49122273 | CCAGCACCTGGCGGG[C/T]GCGATTGCAGAGCGA | 10869 |
rs4279134 | snp | C/T | 0.371987 | 0.218218 | utr-variant-5-prime | USP19 | GRCh38.p7 | 3:49119243 | TTTGGCCACAAAGAG[C/T]TGCCAAGATAGCTGG | 10869 |
rs4292260 | snp | A/G | 0.293415 | 0.246201 | intron-variant | USP19 | GRCh38.p7 | 3:49111457 | CTGGGGAGGAGGATA[A/G]GGGAGGATGGAGGGG | 10869 |
rs4292261 | snp | A/G/T | 0.000198822 | 0.00996888 | missense | USP19 | GRCh38.p7 | 3:49111330 | CATCCAAGTGAAGCT[A/G/T]TGAATGCCCACACAC | 10869 |
rs4355315 | snp | C/T | 3.31625e-05 | 0.00407188 | intron-variant | USP19 | GRCh38.p7 | 3:49111184 | AGCTGCATGACCTCT[C/T]TCCCTGCGAATCTCC | 10869 |
rs4364202 | snp | C/T | 0.347032 | 0.230401 | intron-variant | USP19 | GRCh38.p7 | 3:49113568 | aAATAGggccaggcg[C/T]ggtggctcatgcctg | 10869 |
rs4955411 | snp | C/T | 0.272241 | 0.249009 | downstream-variant-500B | USP19 | GRCh38.p7 | 3:49107871 | CCAGTGCTATCAGCT[C/T]TTTGGAGCCTACCTG | 10869 |
rs6779394 | snp | A/G | 0.350109 | 0.229081 | intron-variant | USP19 | GRCh38.p7 | 3:49120338 | TGACACCTGCCACCG[A/G]CGCCTCCTTCTTGCA | 10869 |
rs6780307 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP19 | GRCh38.p7 | 3:49110040 | CCTCTGGCTAAAGCT[C/T]TGATGTTAAGAGAAC | 10869 |
rs6782515 | snp | C/T | 0 | 0 | intron-variant | USP19 | GRCh38.p7 | 3:49112722 | GGCCCTGCCTTGGGT[C/T]TATGTGGGCAGTGGT | 10869 |
rs6782540 | snp | C/T | 0 | 0 | intron-variant | USP19 | GRCh38.p7 | 3:49112783 | TCTGCTGGCACCTGT[C/T]TCAGTGCCCAATGCC | 10869 |
rs7430082 | snp | A/T | | | intron-variant | USP19 | GRCh38.p7 | 3:49112405 | GCACCTGGGGGCGCT[A/T]GGGTGGGTCGTCTGG | 10869 |
rs11550620 | snp | A/C/G | 0.000231296 | 0.0107516 | upstream-variant-2KB, missense, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49121244 | CTGGCAGGTGTTGTA[A/C/G]ATCTGCACCTGCAAG | 10869 |
rs11552724 | snp | C/G | 0.152186 | 0.230071 | missense | USP19 | GRCh38.p7 | 3:49119040 | AACCAGGAGAGCAAG[C/G]ATGGAGATCCTAGGA | 10869 |
rs12054123 | snp | C/T | 0 | 0 | intron-variant | USP19 | GRCh38.p7 | 3:49119884 | TCAAGAGAAAGTCCT[C/T]TCCCCAGCTGCTGTC | 10869 |
rs13078900 | snp | C/T | 0.5 | 0 | intron-variant | USP19 | GRCh38.p7 | 3:49118539 | cgcagtgagccaaga[C/T]gccactacactctag | 10869 |
rs13321689 | snp | C/T | 0.0138472 | 0.082048 | missense | USP19 | GRCh38.p7 | 3:49111587 | AAGAAATTCCACTGG[C/T]GCTGGGCACAGGACC | 10869 |
rs28612476 | snp | A/C/G | 6.62168e-05 | 0.00575366 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49121578 | GTACTGATCACCCAG[A/C/G]GGACCGCGTAGCAGC | 10869 |
rs34011323 | in-del | -/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | USP19 | GRCh38.p7 | 3:49108369 | AGCTGGCCCTCTGTG[-/T]TGGGTGTCCCAAACC | 10869 |
rs34250378 | in-del | -/C | | | frameshift-variant | USP19 | GRCh38.p7 | 3:49114873 | CTTCCTCAGCTACCA[-/C]CTGAGAGGCAGAGTG | 10869 |
rs34490577 | in-del | -/G | | | frameshift-variant | USP19 | GRCh38.p7 | 3:49115299 | CACGGCAAAGCCAAT[-/G]GGCCAGACGCCCACC | 10869 |
rs34513302 | in-del | -/A | | | frameshift-variant, intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49117323 | TTCTCCTGGCACCGC[-/A]AGCCCCGGCACCAGC | 10869 |
rs34867484 | in-del | -/AT | 0.0116431 | 0.0754054 | intron-variant | USP19 | GRCh38.p7 | 3:49113962 | CACACACATCCACAC[-/AT]GTGATAGCCCAAGGA | 10869 |
rs34991120 | snp | G/T | 0 | 0 | intron-variant | USP19 | GRCh38.p7 | 3:49113935 | ACTGTACACACGTCT[G/T]TGGTGAGTACACACA | 10869 |
rs35088758 | snp | G/T | | | intron-variant | USP19 | GRCh38.p7 | 3:49113907 | CCCATGTGTATGTCT[G/T]TAGATGCCAATGACT | 10869 |
rs35267591 | in-del | -/A | | | intron-variant | USP19 | GRCh38.p7 | 3:49114100 | ACCAGGAACTGTGGC[-/A]AAAAAGGGCAGTCAG | 10869 |
rs35451733 | snp | C/G | | | intron-variant | USP19 | GRCh38.p7 | 3:49113905 | AGCCCATGTGTATGT[C/G]TGTAGATGCCAATGA | 10869 |
rs35565298 | in-del | -/C | | | intron-variant | USP19 | GRCh38.p7 | 3:49113011 | GCTAAAGGCTAGGAA[-/C]CCCTGGGGAGAGCTA | 10869 |
rs35806761 | snp | G/T | 0.0163923 | 0.0890362 | intron-variant | USP19 | GRCh38.p7 | 3:49113938 | GTACACACGTCTGTG[G/T]TGAGTACACACACAC | 10869 |
rs35826923 | in-del | -/G | | | frameshift-variant | USP19 | GRCh38.p7 | 3:49110716 | ACTGCTTACCTAACA[-/G]GGGAACTCCACCAAG | 10869 |
rs58998762 | snp | C/T | 0.0312184 | 0.120974 | synonymous-codon | USP19 | GRCh38.p7 | 3:49113995 | GGACAAAGATACCTC[C/T]GCCAAACGCAGGTTC | 10869 |
rs61729458 | snp | A/G | 0.00762541 | 0.0612745 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49122170 | GGTCAGACCTTGCCC[A/G]CCGTGCATCCTGCAG | 10869 |
rs61734389 | snp | G/T | 0.197531 | 0.244432 | synonymous-codon, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49116543 | CACGTGCACCACCAC[G/T]GAATCCGGGCCCTTC | 10869 |
rs61744082 | snp | A/G | 0.033672 | 0.125308 | synonymous-codon, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49116893 | CTCTGAGCCCAGGAG[A/G]CAGGTTTGGGAGTTC | 10869 |
rs61760207 | snp | A/G/T | 0.00155202 | 0.027814 | synonymous-codon | USP19 | GRCh38.p7 | 3:49111522 | TCGGGACACCCTCTC[A/G/T]CCAGCTGGCAAGGAG | 10869 |
rs61910720 | snp | A/G | 0.00189576 | 0.0307293 | synonymous-codon | USP19 | GRCh38.p7 | 3:49111991 | CAGGAAGGGGTAGCC[A/G]ATGTTCTCAGGTCGG | 10869 |
rs62262518 | snp | C/T | | | stop-gained, utr-variant-5-prime | USP19 | GRCh38.p7 | 3:49116295 | CTGAGCTTCACCTGC[C/T]AACGGAAGGTGGTGT | 10869 |
rs71324937 | snp | C/T | 0.5 | 0 | missense | USP19 | GRCh38.p7 | 3:49114861 | GCCGCTGCCATGCTT[C/T]CTCAGCTACCACCTG | 10869 |
rs71627364 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49122477 | GGGATAGGGGTTTGT[-/T]ACCAGGCATAAGGAT | 10869 |
rs72936820 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant | USP19 | GRCh38.p7 | 3:49108825 | TGCCCCTGCAGGGGC[C/G]ACAACCTCCCCACCC | 10869 |
rs72936885 | snp | C/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121895 | GGTTACACAGATCTA[C/T]GGTTCATGCCCATAA | 10869 |
rs73833525 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | USP19 | GRCh38.p7 | 3:49113156 | ATCCACCACCACAAA[A/G]GGGAATAAACCCTGA | 10869 |
rs74283331 | snp | A/G | | | utr-variant-3-prime | USP19 | GRCh38.p7 | 3:49108158 | TAATGTTTATAATGC[A/G]GGTCAGAAGAATTGA | 10869 |
rs74528938 | snp | C/T | 0.00405406 | 0.0448397 | intron-variant | USP19 | GRCh38.p7 | 3:49111477 | CTCCTCCCCAGCTTC[C/T]AGAGCCTTTCACTGG | 10869 |
rs74951356 | snp | C/T | 0.0422864 | 0.139122 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49121330 | CCTTACTCTCCAGTG[C/T]CCGCTCATTTTCCTC | 10869 |
rs76647653 | snp | A/C/G | 4.97115e-05 | 0.00498535 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121606 | AGCTGCAGATGTAGA[A/C/G]GGTTAGGTTAGCGTG | 10869 |
rs76885631 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49118245 | TGCACTCCAATCTGT[A/G]CAAGAGTGAGACCCT | 10869 |
rs77227194 | snp | C/T | 1.66971e-05 | 0.00288934 | missense | USP19 | GRCh38.p7 | 3:49112393 | TGGGGACGCTGGGCA[C/T]CTGGGGGCGCTAGGG | 10869 |
rs77923560 | snp | A/C/G | 0.000415661 | 0.014411 | intron-variant | USP19 | GRCh38.p7 | 3:49112658 | ACACACAGATCCCAC[A/C/G]TGAGGATAAGCCCTT | 10869 |
rs79274631 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | USP19 | GRCh38.p7 | 3:49112750 | GGTGAGGTCTGTAGG[C/T]CCAAATAGGCTTATG | 10869 |
rs79965514 | snp | A/G | 0.000228702 | 0.0106911 | missense, intron-variant | USP19 | GRCh38.p7 | 3:49109179 | GCTCCTGCCAAATCC[A/G]GGAAGCCTAGGGTAT | 10869 |
rs80060990 | snp | C/G | 0.0320079 | 0.12239 | intron-variant | USP19 | GRCh38.p7 | 3:49112258 | AGGTGGAAAGAAAGG[C/G]TAGGGGAGACCATGG | 10869 |
rs80242485 | snp | A/G | 4.99172e-05 | 0.00499561 | synonymous-codon, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49116779 | CTCCTCCTTGGCACA[A/G]TCATCTTTCCCAGGG | 10869 |
rs80351379 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49118391 | TGGCCAACATGGTGA[A/C]ACCCCGTCTCTACTA | 10869 |
rs111339760 | snp | A/G | 3.31647e-05 | 0.00407201 | synonymous-codon | USP19 | GRCh38.p7 | 3:49110961 | TCACCAGGCCTCCTC[A/G]GGTGCCAGCACCTCA | 10869 |
rs111615620 | snp | C/G | | | upstream-variant-2KB, splice-donor-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121683 | CTCTGCCTCAACCCA[C/G]CTGCTCAGCCTCCTG | 10869 |
rs111935297 | snp | C/T | 1.64749e-05 | 0.00287005 | upstream-variant-2KB, splice-acceptor-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121364 | GGTGCCTTCCAATTC[C/T]AGGAAGGGCAGGTGT | 10869 |
rs112258365 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121647 | GGAGGCCCATCTTCC[A/G]CCCCTACCTTCTCCA | 10869 |
rs112557056 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49122088 | CTCAGCCCAGCTCCT[G/T]GGGAGAAGGGGGAAT | 10869 |
rs112615532 | snp | A/C/T | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime | USP19, LAMB2 | GRCh38.p7 | 3:49121114 | GTCCAGACAACACAG[A/C/T]GGGGGTTCACACTGG | 10869 |
rs112826662 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49121849 | CTCTGCACCTGCCAT[C/T]CTCTCCTGTACCTGC | 10869 |
rs112981471 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49121789 | CAGAGCCTCCAGGAG[A/G]GCATCCAACTGCCGA | 10869 |
rs113123918 | snp | C/T | 0.0599851 | 0.162463 | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49118396 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 10869 |
rs113262645 | snp | A/T | 0.000844867 | 0.0205358 | missense, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49117515 | CTTGCGGGTTTGCAC[A/T]TTAGCACAAGAGCTT | 10869 |
rs113433596 | snp | A/G | 1.68801e-05 | 0.00290512 | synonymous-codon | USP19 | GRCh38.p7 | 3:49111533 | TCTCGCCAGCTGGCA[A/G]GGAGCCAACCTCAAT | 10869 |
rs113592495 | snp | G/T | 0.160642 | 0.233485 | intron-variant | USP19 | GRCh38.p7 | 3:49109223 | TCAGCACCCCGGGGG[G/T]GGGGAGGACCCAGTG | 10869 |
rs114371735 | snp | A/G | 1.66846e-05 | 0.00288826 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49122346 | GTGGCCACCATTTCA[A/G]TGCTATCAGGATCAG | 10869 |
rs114485284 | snp | C/T | 0.00110498 | 0.0234791 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49121527 | TGCAGCCAGCACACC[C/T]TGGGCCTTGCGCTCA | 10869 |
rs114570156 | snp | A/G | 0.0128765 | 0.0791987 | intron-variant | USP19 | GRCh38.p7 | 3:49114756 | TTTCCAGGGGAGCCC[A/G]TCACACCTTGGCACA | 10869 |
rs115838211 | snp | C/T | 0.00260018 | 0.0359629 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121399 | TTAGGGGGGGTTTCC[C/T]GCAGTCTTGTGTCTC | 10869 |
rs116027765 | snp | A/G | 0.00153697 | 0.0276789 | intron-variant | USP19 | GRCh38.p7 | 3:49110650 | AGACAGGCAACAGGC[A/G]CTCAGGATGCCCATC | 10869 |
rs116418928 | snp | C/G | 0.00513281 | 0.050399 | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49116968 | GCAAGATTGTGGAAA[C/G]AATCAGCCCTGGGTC | 10869 |
rs116646690 | snp | C/T | 0.00406852 | 0.0449189 | intron-variant | USP19 | GRCh38.p7 | 3:49115413 | AGGCACTCTCTCTGC[C/T]CATAACCCAGGCTCC | 10869 |
rs116836607 | snp | C/T | 0.0339261 | 0.125746 | upstream-variant-2KB, intron-variant | USP19, LAMB2 | GRCh38.p7 | 3:49121927 | CTTGTCCCACTGATG[C/T]CCTAGGAAGACCTCA | 10869 |
rs117294099 | snp | C/G/T | 0.00402107 | 0.0446583 | synonymous-codon | USP19 | GRCh38.p7 | 3:49114264 | CGGCAGATAAAGAAA[C/G/T]GGGTCAAAAGTGATG | 10869 |
rs138015912 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP19 | GRCh38.p7 | 3:49113391 | AAGCGATTCTCCTGC[C/T]TCAGCCTCCTGAGCA | 10869 |
rs138056152 | snp | C/T | 0.0114369 | 0.0747506 | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49117411 | ACACTGGTATCCCTA[C/T]CCAACCCTGTACTAC | 10869 |
rs138226154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49118160 | GTCAAGCATGGTGAG[A/G]AGGCTGAGGTAGGAG | 10869 |
rs138650227 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP19 | GRCh38.p7 | 3:49112180 | TGGTAAAGTAGGGTG[C/G]CAAGTAGAAAGCTTA | 10869 |
rs138816491 | snp | A/G | 1.65023e-05 | 0.00287244 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49121764 | GACTATTTCCTGCCC[A/G]TTTCAATTTCAGAGC | 10869 |
rs139156815 | snp | A/G | 0.000148369 | 0.00861177 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49121480 | TGCAACAGGTCCCGA[A/G]CCTCATCCCGCAGTT | 10869 |
rs139490252 | snp | A/G | 1.64958e-05 | 0.00287187 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49122836 | CGCTTGCCTGCCGAC[A/G]AGTCTCAGCCACTCT | 10869 |
rs139500325 | snp | A/G | 0.000251604 | 0.0112133 | intron-variant | USP19 | GRCh38.p7 | 3:49109191 | TCCGGGAAGCCTAGG[A/G]TATGTGGAAACGGCC | 10869 |
rs139511264 | snp | C/T | 0.000413083 | 0.0143656 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49121551 | GCGCTCAGCTAGGGC[C/T]TTCACCGTCTGGTAC | 10869 |
rs140057720 | snp | A/G | 0.0107719 | 0.0725942 | intron-variant | USP19 | GRCh38.p7 | 3:49116267 | CACAGTGGTGGGGCC[A/G]GGCACCACCCACCTG | 10869 |
rs140079507 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B | USP19 | GRCh38.p7 | 3:49107960 | CACTTTCAGGGTCTC[C/T]CATATATAAACACAC | 10869 |
rs140142444 | snp | A/G | 6.6024e-05 | 0.00574523 | upstream-variant-2KB, synonymous-codon | USP19, LAMB2 | GRCh38.p7 | 3:49122852 | AGTCTCAGCCACTCT[A/G]CTGAGGATGCTACCA | 10869 |
rs140153123 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP19 | GRCh38.p7 | 3:49120398 | CCCCCATGCCCCAGG[A/G]ACGTCGAGGCGGGTA | 10869 |
rs140729927 | snp | C/T | 4.99172e-05 | 0.00499561 | missense | USP19 | GRCh38.p7 | 3:49111963 | AAGTGAGGCGTGAGG[C/T]AGGTACACTGACCAG | 10869 |
rs141035415 | snp | A/G | 0.00322518 | 0.0400274 | intron-variant, upstream-variant-2KB | USP19 | GRCh38.p7 | 3:49117605 | CATGAGGTAGGATAG[A/G]AGATATCAGAAGATT | 10869 |
rs141267319 | snp | A/G | 0.00433483 | 0.0463533 | intron-variant | USP19 | GRCh38.p7 | 3:49110647 | GTGAGACAGGCAACA[A/G]GCGCTCAGGATGCCC | 10869 |
rs141473691 | snp | A/G | 0.000972947 | 0.0220347 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49121745 | TCTGCTGTAGAGGCT[A/G]CCAGACTATTTCCTG | 10869 |
rs141849414 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP19 | GRCh38.p7 | 3:49114418 | AAACTCTCAGGCTTC[A/C]GGACACTAGACAGGG | 10869 |
rs142037382 | snp | C/G | 0.00227548 | 0.0336536 | synonymous-codon, intron-variant | USP19 | GRCh38.p7 | 3:49109036 | CGCCACGGTGCCCAG[C/G]ACAAAGTACCGGAGG | 10869 |
rs142041381 | snp | C/T | 0.000477937 | 0.0154512 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49121460 | GCAGCTTGTCCTGAG[C/T]GGCTTGCAACAGGTC | 10869 |
rs142857248 | snp | A/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense | USP19, LAMB2 | GRCh38.p7 | 3:49122709 | GGAGGCTCACGGTTG[A/T]GGAAGTCCTTCACAC | 10869 |