| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs181222792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467421 | CATGAACAACAAACT[C/T]CTATTGATCCAGAAA | 51455 |
| rs181229966 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | REV1 | GRCh38.p7 | 2:99427044 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGAGCAG | 51455 |
| rs181232686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99447780 | AGGCTGGTGCAGTGG[C/T]GCCATCTCAGCTCAC | 51455 |
| rs181243194 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99475574 | ATTCTAGAGTCTTTT[C/G]CAATTTTTTAAATGT | 51455 |
| rs181262731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482407 | TACCAAATTATCAAA[C/T]GTGAGGTGTAGTGGG | 51455 |
| rs181283490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462230 | CACAGTTTACAAGTC[C/T]TACTACCCATGTGTG | 51455 |
| rs181290241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421075 | AGTTACTGAGAGCAC[C/T]TGGAGTCAGGGTGAC | 51455 |
| rs181293876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443289 | CAACCTCTGGATTTT[A/C]AACCTAAAATATATA | 51455 |
| rs181306156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478796 | CGTTTCTGATTCAGT[A/G]AGTCTAGGGCAGGGC | 51455 |
| rs181459500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410070 | GGCAGGAGTGCACTG[A/G]CGCGATCTCAGCTCA | 51455 |
| rs181485236 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415910 | TCAAACTGTAATAGT[C/T]GTTGGGGTCAATCCT | 51455 |
| rs181489462 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99466716 | ACAAGATAATACAAA[C/T]GTTTTAGGGGCATGT | 51455 |
| rs181497673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426562 | GTTACAAACAAAAAA[C/T]GAAAACCTTTTTCCT | 51455 |
| rs181500251 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99405614 | GCCTTGCTGAATACA[G/T]TAAGTCTGCATGATG | 51455 |
| rs181501234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99446599 | TCCCAGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 51455 |
| rs181509493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481514 | CTACTACTAGTTTTA[C/G]CTGTCATAAATTGAG | 51455 |
| rs181513866 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | REV1 | GRCh38.p7 | 2:99437229 | CTCAAGCAATCCTCC[A/C/T]GCCTCGGCCTCCGAA | 51455 |
| rs181571317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474677 | GAGGCTGAGGCAGGC[C/G]AATCACATGAGATCA | 51455 |
| rs181602719 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99429346 | GTGCTAACAAGTTGA[C/T]AACACTCTTAACACT | 51455 |
| rs181705544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456866 | AGGCAAAAGAACAAA[C/T]AGAAACACAGAACTG | 51455 |
| rs181836124 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99470303 | TTAACTAATGAAATT[C/T]ATTTTGAGTGGCTTT | 51455 |
| rs181849723 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99487635 | CAGTTGGTGCTATTA[C/T]AGTAAAAAAAAACTT | 51455 |
| rs181863083 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400812 | TGGAACAAGTAGAAT[C/T]CCGGTCTGAGACCTC | 51455 |
| rs181884448 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99442145 | TAAGCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51455 |
| rs181884881 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | REV1 | GRCh38.p7 | 2:99447991 | ATGAGCCACCATGCC[C/T]GGCCAAGCATAAAGT | 51455 |
| rs181889526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407410 | ACAAAAAATTAGCTG[A/G]GCGTGGTAGCGGGTG | 51455 |
| rs181895240 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99427805 | TAAATTCATTTTCAT[A/C]ACTTTATGTATCTTC | 51455 |
| rs181906372 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99467773 | ATCGTGGGCCAGGCG[C/T]GGTGGCTCACCCCTG | 51455 |
| rs181909608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483233 | CAAAAAATCTAAGTA[A/G]TTTCAACTACATAAC | 51455 |
| rs182021795 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99460983 | GGGTGCTCTCTTGAA[C/T]TGGAGACTTCCATGA | 51455 |
| rs182143175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99455968 | ATGTACTAAAGGAAG[C/T]AGAAAATAACCTGAA | 51455 |
| rs182164092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412049 | CCAGCCTGGCCAACA[C/T]GGTGAAACCACGTCT | 51455 |
| rs182317664 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99415350 | TCAAGGAGGCTCCTG[A/G]TCAAGCAACTGGGAC | 51455 |
| rs182326230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478110 | GGTGGTGCACACCTG[C/T]AGGTAGTCCCAGCTA | 51455 |
| rs182327989 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99411014 | AAACGTGGCCAGGCG[C/T]GGTGGCTCACACCTG | 51455 |
| rs182382211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453952 | ATTCAGGGAAATTCT[A/G]TCCTCCAAATTTTTA | 51455 |
| rs182402279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471367 | TTCAACAAATGGTGA[C/T]AGGAAAACTGGATAT | 51455 |
| rs182403689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432428 | CTGATAATGACCCAG[A/G]GAAAGAAAGATCAGG | 51455 |
| rs182416916 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99489334 | GAGCGGCGGCTCGAC[A/C]GGGTCGACATTCTAC | 51455 |
| rs182417820 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99473995 | TTTATAAAAGCAATT[C/T]GTGTTTATTGCAGAA | 51455 |
| rs182433578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99402037 | GCCCAGCCCACTTCC[C/T]ATGGTTTTTTAATCA | 51455 |
| rs182555629 | snp | C/G | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99444698 | ATTTGAAGCCTAAAC[C/G]ACTATCTATCAGTTG | 51455 |
| rs182589693 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480079 | ATCTCAGCACTTTGC[A/G]GGGTTACGGCAGGAG | 51455 |
| rs182590615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99436195 | AAAAATACAAAGGTG[C/T]TGGCATACATTTAGT | 51455 |
| rs182613339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99416209 | TCCACAAGATATAAA[C/T]AGGTACTGTATATTT | 51455 |
| rs182631425 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457804 | GGCTTACCACATAGG[A/C/T]ACAGTATTTGATATA | 51455 |
| rs182634516 | snp | G/T | 5.0571e-05 | 0.00502822 | intron-variant | REV1 | GRCh38.p7 | 2:99408162 | TTAAAAAACAAAAGC[G/T]TCATTCCATATGTAT | 51455 |
| rs182656377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437645 | TCTACCAAATGCTTT[C/T]ATACAATAACAAAAT | 51455 |
| rs182682797 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99411891 | AGAGGGTAATTAACT[A/C]ATCACATTTCAAATC | 51455 |
| rs182974874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440890 | GGAAAATACATTGTT[A/T]ACATACATTCTTGCT | 51455 |
| rs182975848 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468129 | AGGTTGCGGTGAGCC[A/G]AGATTGCACCATTGG | 51455 |
| rs182980184 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99459024 | CCATACTGGCTAACA[C/T]GGTGAAACCCCGTCT | 51455 |
| rs182988738 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484043 | TGTAAAAACATCCCA[C/T]CTATGTGTTCCTCCT | 51455 |
| rs182990390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99468048 | AGCCGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 51455 |
| rs182991573 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99417979 | CATTTCTGACACTAA[C/T]ACATCGTTTTAAGTT | 51455 |
| rs183038712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425205 | TATATACAAACAGTT[A/G]CCAATTACTCATAGG | 51455 |
| rs183051415 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99453488 | TTCACACAAAACATT[A/C]AATTTTGCAATTCAT | 51455 |
| rs183062942 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99488791 | CTAAACAGGAAATGG[C/T]TTATTCTCGGAGACT | 51455 |
| rs183196477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444186 | CTGTGGTATTATGTA[C/T]ATCAAACTCACTTGC | 51455 |
| rs183207935 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490501 | CCGGGCTTCAAACCC[C/T]GGTACTGTGTGAAGA | 51455 |
| rs183209125 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | REV1 | GRCh38.p7 | 2:99403282 | TACAGGCTCTCCAAT[C/T]CTCTCTTTGCTTTGC | 51455 |
| rs183211455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99424366 | TGATATCTCCCCATG[C/T]CACTAATTTATAATT | 51455 |
| rs183228361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463664 | GGTCTTGCTGTTGTC[A/G]CCCAGGCTGGAGTGC | 51455 |
| rs183266427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484261 | AAACGAGCAGAAAAA[A/G]TAACTATTGTGTATC | 51455 |
| rs183270547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99448966 | CACCCTGTCAATCAG[A/G]AGGCAATATATTAGT | 51455 |
| rs183284895 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431900 | GGGCACATGGAGAAT[A/G]TGGAGGAACGGTTGG | 51455 |
| rs183307465 | snp | C/G/T | 0.000494253 | 0.0157134 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403756 | TTGTCTTTGATCATA[C/G/T]GCTGCTTTCAGCTCC | 51455 |
| rs183312176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99470643 | TTTCTCTACATTCCA[C/T]AAGTTACTTCCTCCT | 51455 |
| rs183327797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407824 | GGAAAAGTACAGTAA[G/T]AATCTAAGAAAATTA | 51455 |
| rs183440359 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99468348 | TAAATAGGACTTTCC[C/G]TAGAACGGAGGAGGG | 51455 |
| rs183466370 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484702 | AAATCTAAAAAAAAA[A/C]CAAAAAATTAGCCAT | 51455 |
| rs183550327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99427949 | AAATTTATATTTACC[A/G]TGGGTAAATATAAAT | 51455 |
| rs183556668 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99448530 | AACAGTAAATAATAC[C/T]GCGACTGTACTCCCT | 51455 |
| rs183570160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476412 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCACA | 51455 |
| rs183648345 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99471850 | GCAAATAGAAACCAC[A/C]ATGAGATACCACCTC | 51455 |
| rs183737771 | snp | A/G | 9.8912e-05 | 0.0070318 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435876 | CCACTGATACAAAGA[A/G]GCAATCCATATCAAC | 51455 |
| rs183748755 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99415206 | AATTAAGTAGGTGTT[G/T]ATAAGGGAAAGATGG | 51455 |
| rs183754197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473819 | ACAGGTTTTGGTACA[A/T]AAGCCTTTTCTTGAA | 51455 |
| rs183764497 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99455643 | GATGAGAGTCTCACA[A/G]GAAATGGAAGGAGAG | 51455 |
| rs183815828 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | REV1 | GRCh38.p7 | 2:99410071 | GCAGGAGTGCACTGG[C/T]GCGATCTCAGCTCAC | 51455 |
| rs183815962 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99459352 | GGGTTCACAGTATCA[C/T]TATGTGCTATGTCTT | 51455 |
| rs183819245 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99429695 | TGGGGGGTTGTGGGG[A/G]GCATAGATGAGATGA | 51455 |
| rs183821531 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99476698 | ACCTCCTGAAGGGCT[A/G]AAAACTAAAGGTCAA | 51455 |
| rs183870925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433497 | CAGAGATGTTCGCTG[C/G]CTTTCCTTTTGCCTT | 51455 |
| rs183918503 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99458989 | CAAGGTGGGCAGATC[A/G]CGAGGTCAGGAGATC | 51455 |
| rs183928054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417395 | ATGATCCATCTGCCT[C/T]GGCCTCCCACAGTGC | 51455 |
| rs183973924 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99441662 | AAAAATATAGCTGGT[A/G]CAGTTAGTTCCATTT | 51455 |
| rs184026276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99479991 | AGGGGTGACATGAAG[G/T]CAAAGATTTCAGGAA | 51455 |
| rs184030607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454368 | CAAGTCTGACCAACA[G/T]GGAGAAACCCCGTCA | 51455 |
| rs184032192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99434625 | CCATGTAAATGTCAT[C/T]TAAGTTTCTTAGCAC | 51455 |
| rs184041416 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99413137 | ATGCTAGTAGATGTA[C/T]TTCTAGACTCTACTT | 51455 |
| rs184051317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414281 | CTCTGGAACCAGTAT[A/G]TAACACAAGGTTAGG | 51455 |
| rs184108210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476217 | CCTTTCTTTTCCCCC[C/T]CTTCACATGGTCCAA | 51455 |
| rs184255385 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | REV1 | GRCh38.p7 | 2:99466717 | CAAGATAATACAAAC[A/G]TTTTAGGGGCATGTG | 51455 |
| rs184444706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481954 | GTGTCTTTGTTATCC[A/G]TGAATCCATAATGGG | 51455 |
| rs184469968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99404747 | GTTTGGGAGTTAACA[C/T]GCCACTTTAAATTTC | 51455 |
| rs184491233 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480616 | TCTCTGAACTCACAA[A/G]GTAACTGGCATAAAC | 51455 |
| rs184493708 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99445090 | CATCTATTTTGGGAA[G/T]TCTTACTCTTGCTTT | 51455 |
| rs184581653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469661 | TATCAAGAGTCTCAT[C/T]AAGGACATGCTTATT | 51455 |
| rs184588896 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99425671 | TAAATTTCAGGTAAT[A/C]ATTATGCCAGATATA | 51455 |
| rs184633427 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | REV1 | GRCh38.p7 | 2:99465832 | CTTATATATTATCCA[C/T]GTCAAATCAGCTCTG | 51455 |
| rs184682000 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99462043 | AGGTCCTTTCCTTCC[A/C/T]TGCTTGGCGACCCAA | 51455 |
| rs184682373 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485618 | AAAAGCCACTCTGGT[A/G/T]GGCGGTTGTTGAGAT | 51455 |
| rs184688326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99452050 | CCAAAAGAACATACA[C/T]GATAACTGCAGATTT | 51455 |
| rs184693371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478584 | TAGAAAAGTTCAAGG[G/T]TGCAATAAATCAGGG | 51455 |
| rs184696041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99442607 | TTATTCCTTCTTGCT[C/T]GGTTTTAGTGGTCCT | 51455 |
| rs184725752 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99466028 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACA | 51455 |
| rs184729389 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99486021 | TGCAGGCTACTCGAG[A/C]GCCTGAGGCGGGAGG | 51455 |
| rs184738405 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | REV1 | GRCh38.p7 | 2:99445635 | AATTTCAAGGTAAAA[C/T]TGTCTCAAGACAAAG | 51455 |
| rs184754511 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481251 | AATTCAAGACCAATA[C/T]CAAAATTCAGATTTT | 51455 |
| rs184835369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455098 | CCTAGCTAGATCTCT[A/G]TTGAGAAAACATTTA | 51455 |
| rs184874411 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491278 | ACAAATTGCGTAATT[A/G]CTTTCTTTTCTTTTC | 51455 |
| rs184881350 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99419037 | AGGTTATCCATCAAG[G/T]TTCTAAAAACAATGA | 51455 |
| rs184892328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405151 | TGAGAGCAGCACACT[C/G]GAAGAAAGGGTTTCT | 51455 |
| rs184900221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426226 | GTGGCACACTCCTGC[A/G]ATCCCAGCTACTCGG | 51455 |
| rs184941537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99409009 | AATAACCACTAAAAG[C/T]TGAGCACAGTGGCTC | 51455 |
| rs184946728 | snp | C/T | 0.000122244 | 0.0078171 | intron-variant | REV1 | GRCh38.p7 | 2:99405896 | TACTTATATTTAGGA[C/T]TACAAAAATGTACCT | 51455 |
| rs184961587 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | REV1 | GRCh38.p7 | 2:99446602 | CAGGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTC | 51455 |
| rs184965600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472207 | GGTATATACATACAA[C/T]GAAATACTATTCAGC | 51455 |
| rs184983362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99449979 | AAAAGGAGACTTACT[A/G]TAGGGCTTATTAGTA | 51455 |
| rs184985637 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | REV1 | GRCh38.p7 | 2:99469972 | TAAAAATACAAAAAA[G/T]TAGCCGGGCATGGTG | 51455 |
| rs184996344 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99452984 | CACATGTAAACTGGG[A/G]ATAATAATAGTGTCT | 51455 |
| rs185000737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486608 | TAATCCTGTGAGGTA[G/T]GTATTATTACAGTCA | 51455 |
| rs185236073 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407251 | TGCACCACCACACCC[A/G]GCTAATTTTTGTATT | 51455 |
| rs185274872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99409358 | ATGCACCATGTATGG[C/T]TGGCATGAGCTAATC | 51455 |
| rs185296333 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99451017 | AACTACAGCATCAGA[A/G]TGATTTAATGTGAAA | 51455 |
| rs185323730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99476012 | ATGAAAATAAACAAA[C/T]GTGTATGATTCTACA | 51455 |
| rs185425989 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99468883 | GAGTGAGACTACACA[C/G]GTGGAAACCCTTTGA | 51455 |
| rs185434622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428743 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 51455 |
| rs185489522 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99457820 | ACAGTATTTGATATA[A/G]TGTGGTACTGGTGAA | 51455 |
| rs185502591 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99437719 | TTAGAAGCATTAAGA[A/C]TTAAATAACCTTCAG | 51455 |
| rs185533242 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411955 | CAAGACATATCCAGC[C/T]GGGCGCAGTGGCTCA | 51455 |
| rs185538933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99462944 | AATACAAAAATTAGC[C/T]GGGTGCAGTGCCAAG | 51455 |
| rs185566873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478948 | AAAGGTTATATACAG[C/T]AGAGAGAATGATGCT | 51455 |
| rs185570965 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432158 | ACTGAGTACTGCTCA[A/G]GAAGCAGCCTCCAAA | 51455 |
| rs185580295 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453530 | CAAATCCTTCTCTTG[C/T]TGCCCACCCTTCAGT | 51455 |
| rs185604102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99419720 | GGCAGTGAGGTTCAC[A/G]GTGTAGGTGTGGGCA | 51455 |
| rs185649734 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459995 | CAACAAGAAGGGACA[C/T]CACAGCTTCTTTTAC | 51455 |
| rs185776830 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | REV1 | GRCh38.p7 | 2:99442122 | CCAGGCGTGGTGGCA[C/G]ACGCCTGTAAGCCTA | 51455 |
| rs185780862 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | REV1 | GRCh38.p7 | 2:99477809 | ACTACCAAAAAAAGA[C/T]GCTTGATTTAACAAA | 51455 |
| rs185784028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415960 | GATCATATTAAGAAA[C/T]GTATTTATTAGTGTA | 51455 |
| rs185811172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484076 | TTGAAGGAGATCCAG[A/G]TAAAGATCTCCTATG | 51455 |
| rs185866075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463516 | CAAGAGCAAAACTGC[A/G]TATCAAAACATAGTA | 51455 |
| rs185876012 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99423456 | AACTGAGAACTTCTG[C/T]TGAGTGACAGAAACT | 51455 |
| rs185984760 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99444109 | ACAGGTGTGAGCCAC[A/C/T]GCGCCCAGCCCTTTT | 51455 |
| rs186012499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99479474 | TATAGTTTTCAAGGT[C/G]AGTAAAATGAGAATA | 51455 |
| rs186014781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437369 | AGAAAACTAAGACTC[A/G]GAGAGGTGAACTAAC | 51455 |
| rs186020800 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99457082 | TCCCAAAGGCAATTG[G/T]TTCCTCTTCTGTGTT | 51455 |
| rs186086987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99427812 | ATTTTCATCACTTTA[C/T]GTATCTTCTTAAACA | 51455 |
| rs186097128 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99448030 | TTATACCAGGTTATA[G/T]GGATACTGAACTGCC | 51455 |
| rs186099426 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | REV1 | GRCh38.p7 | 2:99407508 | AGTGAGCCGATACAA[C/T]GCCATTGCACTCCAG | 51455 |
| rs186106843 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447854 | GCCTCCCAAGTAACC[A/G]GGATTACAGGCACAA | 51455 |
| rs186112770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416664 | GGGCACGGTGGCTCA[G/T]GCCTATAATCCCAGC | 51455 |
| rs186129754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99467918 | GGGCACGATGGCTCA[C/T]GCCTATAATCCCAGC | 51455 |
| rs186131233 | snp | A/T | 0.287606 | 0.247155 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483035 | AAAAAAAAAAAAAAA[A/T]TTTTTTTTTGTTACG | 51455 |
| rs186133239 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483780 | GGGAACAGTTTGGTG[C/T]AGCAGGGGGAAAAAA | 51455 |
| rs186154190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401639 | ATAATCCCAGCTACC[C/T]GGGAGGCTGAGGCAG | 51455 |
| rs186202460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443818 | TTCGACTATTTTTTA[C/T]TTTATTCTTCCTCAA | 51455 |
| rs186220725 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99400991 | GTAAACACTTCACTG[C/T]AAAAATCCATAAAAC | 51455 |
| rs186221048 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99420756 | GAAGATGGAGGAATA[A/G]TGGTTGAAAGTGACA | 51455 |
| rs186222105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470893 | AAATGGCCTTGCTGA[A/G]GAAATTAAATTTATG | 51455 |
| rs186253128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427167 | AGCCTGGGCAAAAGA[A/G]CAAGACTTCATCTCT | 51455 |
| rs186276448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467569 | TCCTAGAAGAGTGGC[C/T]GGGAGACTGGGCAAA | 51455 |
| rs186345798 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99421211 | CCTAGCTTTAAATAC[A/G]GTTTCCGTTCACTTT | 51455 |
| rs186349510 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430133 | GTTCGCTTCCATTAT[A/G]TTCTTCATCAGCAGA | 51455 |
| rs186366497 | snp | A/G | 0.00280918 | 0.0373724 | intron-variant | REV1 | GRCh38.p7 | 2:99410884 | TATGGAAAGACAAAC[A/G]TGGAGAAACTACCAT | 51455 |
| rs186403272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488957 | TAGTACATGGCGTGA[A/G]AAGACGTGGAGATAA | 51455 |
| rs186692049 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99459886 | AGGTATAGGGACTAC[A/G]AAATCATGAGAGGCT | 51455 |
| rs186695804 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99476817 | TCTCCATGAGTAGTG[C/T]CACACATCAGTGCCA | 51455 |
| rs186697641 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | REV1 | GRCh38.p7 | 2:99468049 | GCCGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 51455 |
| rs186723732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454079 | GTCACCCAGGCTAGA[A/C]TGCAATGGCTCTATC | 51455 |
| rs186732722 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99425796 | AATCCCAGCACTTTG[C/G]GAGGCCGAGGCAGGC | 51455 |
| rs186734874 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99471378 | GTGATAGGAAAACTG[G/T]ATATCACATGCAAAA | 51455 |
| rs186736755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432924 | CTACTCCTAAGGAAT[A/G]TGAGCTTGTCAAGGT | 51455 |
| rs186740938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404847 | CACATTTTTGGAACG[C/T]CTTGGCCTTTTGTCA | 51455 |
| rs186748703 | snp | C/G | | | upstream-variant-2KB, intron-variant | REV1 | GRCh38.p7 | 2:99490085 | TTCCGCGCGCGCTCC[C/G]CGGCCCCGCTCGCGC | 51455 |
| rs186883403 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99475001 | TAATCAGTCATATTT[C/G/T]AGTTCCTCCGTATGT | 51455 |
| rs186907816 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480222 | CAGCTACTTGGGAGA[A/G]TGGGATGGGAGAACT | 51455 |
| rs186949726 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99411279 | GGCGACAGAGGGAGA[C/G]TCCGTCTCAAAAAAG | 51455 |
| rs186965664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408442 | CTAACATATGCACAA[A/C]TAAATACATATTTTC | 51455 |
| rs186968586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487804 | TACCTGTCACCTCTT[C/G]TGATTACCTTTCCTC | 51455 |
| rs186969998 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99428632 | CTATTATGATTAGAC[A/G]ATGCTGAGCTCAAAT | 51455 |
| rs186972642 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99453294 | AACCCAGGAGGTAGA[A/G]GTTGCAATGAGCTGA | 51455 |
| rs186990518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99436443 | TAAGTCACATAGCCT[A/G]TTATTAAATGGTTGA | 51455 |
| rs187025541 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99474598 | CCATCTAGACCCCAA[C/T]TAGTCCATATTGATA | 51455 |
| rs187129113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99431194 | AGCATTTCTGGATTT[C/T]GGCAACCATATATAC | 51455 |
| rs187169227 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | REV1 | GRCh38.p7 | 2:99470405 | CAGACTCTCCTCCCC[A/G]TGTAATTAGGAATAA | 51455 |
| rs187195165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99415557 | GATGGAAATGTTCTC[A/G]TCTGCTATCCAATAC | 51455 |
| rs187225243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456489 | GGTCTCCGTAAAAAG[G/T]TAACATTTGAGCAGA | 51455 |
| rs187306637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99441018 | TGTATTAAGAAGTAA[A/C]ATCTAAAAGGTAATT | 51455 |
| rs187322557 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99418054 | AATGCCATTTCTGTC[A/G]TTTAATATTTATGGC | 51455 |
| rs187324135 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99476442 | ACGCCGGTAATCCCA[A/G]CTACTCAGGAAGCTG | 51455 |
| rs187339636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99459030 | TGGCTAACACGGTGA[A/C]ACCCCGTCTCTACTA | 51455 |
| rs187393915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99463913 | ACAGGTGTGAGCCAC[C/T]ACGCCCAACCTCAGA | 51455 |
| rs187397171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99479998 | ACATGAAGGCAAAGA[C/T]TTCAGGAAGAAGAAA | 51455 |
| rs187527365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99444285 | TTATCATAGATAGCT[A/G]TAACTAAGAGACAAG | 51455 |
| rs187533383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99403315 | CTTACTAATTTGACC[A/T]TTGGCATGTTGCTCA | 51455 |
| rs187536469 | snp | C/T | 0.00349693 | 0.0416682 | intron-variant | REV1 | GRCh38.p7 | 2:99424738 | CACAAAACAGTGCTA[C/T]GTGACAAACAGACAA | 51455 |
| rs187558629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465914 | TACCCCACACACATT[A/G]GCAGATAATTTCTTT | 51455 |
| rs187605632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484309 | GATGAAACAATCTGT[A/G]CAACAAACCCCCATG | 51455 |
| rs187610008 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99449663 | GGTAAATCACAAAGT[A/G]AGAAAGCTATGTTGC | 51455 |
| rs187751193 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99409046 | GTAATCCCAAAACGC[C/T]GGGAGGTCAAGGCAA | 51455 |
| rs187775571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412063 | ACGGTGAAACCACGT[C/G]TCTACTAAAAGTACA | 51455 |
| rs187778997 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99468712 | ACTTTAACAGGGCAG[C/G]CAATTACTGTGTTTC | 51455 |
| rs187789193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428721 | TGTAACTAGGCCAGG[C/T]ACAGTGGCTCACGCC | 51455 |
| rs187795027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450791 | ATATTTACTTTCTTT[C/T]TTCTTCTTAAATCTC | 51455 |
| rs187831613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480921 | AAGTCTTATTCAATG[A/T]AACAATTTAGCACAC | 51455 |
| rs187833546 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99445243 | TAAACACTGAATGTA[A/C]TTAGAAACCAAAGTT | 51455 |
| rs187858098 | snp | C/T | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403794 | GTTCAGCAGGAAGGG[C/T]AGCAAATACCTCAGG | 51455 |
| rs187869497 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468177 | AAGAGCGAAACTCCA[A/T]CTCAAAAAAAAAAAA | 51455 |
| rs187872408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99444750 | TTGCCCATTTATCTA[C/T]CTATAGATATATAGA | 51455 |
| rs188001280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99484856 | CCTCGGGAACTGGCC[C/T]GAAATCTTGCCTCCT | 51455 |
| rs188115358 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99425405 | GGAAAATGACAGAGT[A/T]GTAAAGAAAACAATT | 51455 |
| rs188145808 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99455887 | AAGTACTTGTCCGGG[A/C]CCCCCTCCACCTGCT | 51455 |
| rs188154122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99473915 | TTATACACTGCTTTG[C/T]AATGCTAAGTACAGT | 51455 |
| rs188161558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464424 | TCCTATTCATTAAAA[C/T]TTTGGGGTGTTGTTT | 51455 |
| rs188183122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429734 | AAAACCTCATAACAC[A/G]TCTGTAACATTTAAA | 51455 |
| rs188188556 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99452099 | TGTATTTAACACTCT[C/G]CTTTAATTCAGCAGA | 51455 |
| rs188192910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99410161 | GACTACAGGCGAATG[C/T]CACCATGTCCGGCTA | 51455 |
| rs188281629 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428165 | AGGGTAAACGGAGCT[C/T]GCATTTTACCAACTA | 51455 |
| rs188384030 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99454370 | AGTCTGACCAACATG[A/G]AGAAACCCCGTCACT | 51455 |
| rs188394303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99413861 | GTTGTGTTTCTGGTC[C/T]TCTGTAGGAACTTAT | 51455 |
| rs188404157 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490564 | ATTGATTTACAGTGA[C/T]ATCTAGTGGAGAAAG | 51455 |
| rs188424900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434782 | AGATTCAGACTTAAG[C/T]AGTGGGGAAAGAAAA | 51455 |
| rs188436393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455170 | TAATTGTTGACTGTG[A/C]TATATAAATCACAGA | 51455 |
| rs188446271 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99414302 | CAAGGTTAGGAAGTC[A/T]TCAATGTGGGTCAGA | 51455 |
| rs188580248 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99407913 | TGTATTACAAAGCAG[C/T]TAAAGACCTACATAT | 51455 |
| rs188598576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448558 | CCTCCTTTCCCCCTA[C/T]TCCTAGCATTCTAGG | 51455 |
| rs188628672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439427 | CCCCTTTAAAAACAG[A/G]AAATTCTTATATTGA | 51455 |
| rs188647945 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472338 | TGATTCTACCTATAT[G/T]AAGTATTTAAAGTAG | 51455 |
| rs188657997 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99476226 | TCCCCCCCTTCACAT[A/G]GTCCAAGATGAGACT | 51455 |
| rs188684130 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433525 | CTTAATTTCATTGGA[A/G]TCATTGTGACAAGCC | 51455 |
| rs188694361 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99471902 | ATTAAAAAAAAAAAA[A/C]AAAAAAAAACAAGTG | 51455 |
| rs188914212 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99459011 | CAGGAGATCAAGACC[A/G]TACTGGCTAACACGG | 51455 |
| rs188920692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417696 | AGAACTGTGAGACAA[C/T]GCATTTCTGTTGTTT | 51455 |
| rs189026693 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401146 | AAGAAATTTAAAATT[A/G]TAAAAACTCCGAGCA | 51455 |
| rs189051247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462188 | ACATCTAGAGATTTA[C/G]CAATGAAATGGACCT | 51455 |
| rs189061312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478738 | CATCAGAATCACTAG[C/G]ACAGGGCCTGTTAAA | 51455 |
| rs189069536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99442763 | ATCAAAATCTCATCT[A/G]TTAAGGTTTTCCAAG | 51455 |
| rs189075719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405390 | TTTAACATCTCCTTC[C/T]GCCTCCTTCCATGCA | 51455 |
| rs189103789 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99466141 | TATTTTTAGTAGAGA[C/T]GGCGTTTCACCATGT | 51455 |
| rs189114553 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | REV1 | GRCh38.p7 | 2:99426291 | GGTGGAGGTTGCAGC[A/G]AGCCAAGATCGTGCC | 51455 |
| rs189120867 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99446577 | TCGGCTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 51455 |
| rs189130931 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99436004 | TTAAAACATCAGGTC[C/T]AGTTAATTTTAGAAA | 51455 |
| rs189132321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481481 | TTTAATACAACAGAG[A/G]TAACTGGGTTACTAT | 51455 |
| rs189177802 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | REV1 | GRCh38.p7 | 2:99419400 | CTGTATTTTTACAGA[C/T]GGGGTTTCACCATGT | 51455 |
| rs189243812 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99486195 | ATACAAAATCCTAAG[G/T]GAACAAGCTAATTTC | 51455 |
| rs189258932 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483230 | GAGCAAAAAATCTAA[A/G]TAGTTTCAACTACAT | 51455 |
| rs189364480 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400773 | GAGACAAGAATAAGA[C/T]GGTTTAGAAGCTTTA | 51455 |
| rs189426049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431078 | ACGTTAATGCACCAC[C/T]AGGAAAACTGGCAAA | 51455 |
| rs189427324 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99415286 | ACCTATTAAGGAAAA[G/T]GTGAAGGAAAATATG | 51455 |
| rs189461512 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99453104 | AGTGGCTCACACCTG[C/T]AATCCCAGCACTCTG | 51455 |
| rs189463633 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | REV1 | GRCh38.p7 | 2:99486953 | TCACCTAGTAATAAA[C/T]GCTATGGAGAAAAAG | 51455 |
| rs189468322 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99442084 | TGGTGAAACCCCGTC[G/T]CTACTAAAAATACAA | 51455 |
| rs189513503 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99469761 | TATCAGTTCATTCTA[A/C]ACTTTATTCTGCTTT | 51455 |
| rs189685897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476070 | AACACATACATATTA[C/T]GCAACTTTACGTAAC | 51455 |
| rs189686201 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99447098 | GGATGTTATAGGGAC[A/G]AGCCTTTGACTTTAT | 51455 |
| rs189696740 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | REV1 | GRCh38.p7 | 2:99447987 | AGGCATGAGCCACCA[C/T]GCCCGGCCAAGCATA | 51455 |
| rs189706365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407330 | CTGAGGTGGGTGGAT[C/T]ACCTGAGGTCAGGAG | 51455 |
| rs189712270 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427261 | AAAGTAAGAAAGGTA[G/T]TGGGTCCTTACAAAA | 51455 |
| rs189906892 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99412002 | ACTTTAGGAGGCTGA[A/G]GCGGGCAGATCACAA | 51455 |
| rs189935640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432318 | ATATAAGCCAAACAT[G/T]AGAACTGATCTTTTT | 51455 |
| rs189939896 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99470911 | AATTAAATTTATGTT[C/T]AAGTGCTACTTCTTT | 51455 |
| rs189948910 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | REV1 | GRCh38.p7 | 2:99453850 | GTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 51455 |
| rs189955735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99467413 | ACTTGACTCATGAAC[A/G]ACAAACTCCTATTGA | 51455 |
| rs189957084 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99429195 | TTACAACTATTCCAA[G/T]TATTTCAAAACGGTT | 51455 |
| rs189959898 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99426897 | AACAATATTAAAAAA[C/T]TGCTGGCCGGGTGCG | 51455 |
| rs189976437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468964 | ACAACATAATGATAA[C/T]AGTAGACTAGATACG | 51455 |
| rs190011617 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99415696 | CTTCACTTGGCTACG[C/T]AGCTACTGTATTAGT | 51455 |
| rs190058110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456598 | TGGCAAGGGATTACT[A/G]TACATAAAACAGGCT | 51455 |
| rs190153464 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99489141 | ACAGTACAGAAGTGG[A/G]CAAGGGGCTCTCGGA | 51455 |
| rs190174624 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | REV1 | GRCh38.p7 | 2:99409590 | GGCTCATGCCTGTAA[C/T]CCCAACACTATGGGA | 51455 |
| rs190195679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451701 | GAAAACTGCTATTAT[C/T]ATAAACTATGATCAC | 51455 |
| rs190218205 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99485759 | ATCCACAAAATGTAT[C/T]TTTTAAAGGCGTTCC | 51455 |
| rs190303284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99436459 | TTATTAAATGGTTGA[A/G]CTGTGATTCTGTCTC | 51455 |
| rs190306494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424958 | CCACATTACCTTTGA[C/T]ATTTGGAGCATTCAC | 51455 |
| rs190308707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99474635 | AGTCGGGAGCGATGG[C/T]TCACGCCTGTAATTC | 51455 |
| rs190310528 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99444538 | ATTCTTAGGCTTACA[G/T]AAGTCAGTCCATGGA | 51455 |
| rs190317640 | snp | A/C/T | 3.29648e-05 | 0.00405974 | intron-variant | REV1 | GRCh38.p7 | 2:99403657 | GACTCCATTACTCTT[A/C/T]GTCTTCATTTTTGTT | 51455 |
| rs190345982 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464094 | ATCTAATCAATCTAT[C/G/T]TGATAGTAATATTAA | 51455 |
| rs190350016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480025 | GAAAAATTCATAATT[A/G]AAAACATAAAAGGGC | 51455 |
| rs190356788 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99416010 | TGGAGTCTCCTAAAG[C/T]AAAAACTTACTATTG | 51455 |
| rs190369687 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99457425 | ACTGGCTCACACCTG[C/T]AATCCCAGCACTCTG | 51455 |
| rs190383605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475156 | CAGTTTTGCCATGAG[A/G]GTACAAGGAACAAAG | 51455 |
| rs190385437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437588 | AACAACTCAAAATAA[C/T]GCTTTTAAACATTCA | 51455 |
| rs190498646 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99442125 | GGCGTGGTGGCACAC[A/G]CCTGTAAGCCTAGCT | 51455 |
| rs190502688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478080 | TTTATAAAAATACAA[A/C]AATTAGCCGAGCGTG | 51455 |
| rs190519545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420052 | GGATTCACATGATCA[C/T]TTATAAATGAAAATT | 51455 |
| rs190548775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99427881 | TATTCTGTCCTCATA[C/T]AGTCACCCCAATTAT | 51455 |
| rs190557397 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99448516 | TATAATCATTAAAAA[A/G]CAGTAAATAATACTG | 51455 |
| rs190594737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467946 | AGCACTTTGGGAGGC[C/T]GAGGTGGACAGATCA | 51455 |
| rs190594849 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483859 | CAGGCAAATGACTCT[C/T]GGGGTCTCACTTTCC | 51455 |
| rs190601027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467651 | AAGGATAAAGATTGC[C/T]GCAATTGCTATCAGA | 51455 |
| rs190609030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437873 | ATAACAGAAAACACC[C/T]CACATAGAGTCTCTA | 51455 |
| rs190759503 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | REV1 | GRCh38.p7 | 2:99460168 | TTCAACCTCCGCCTC[C/G]CGGGTTCAAGTGATT | 51455 |
| rs190837980 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99463225 | AAAAAGCTAAGTCAA[A/T]AATAATAATACTGGC | 51455 |
| rs190840916 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99457840 | GTACTGGTGAAGGAA[A/C]AGACACAAACATCAA | 51455 |
| rs190842243 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99421315 | TAACTTATTTATTGC[A/G]AAGATTATCAACCAT | 51455 |
| rs190852785 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | REV1 | GRCh38.p7 | 2:99416868 | CAGTGAGCCGAGATC[A/G]CACCATTGCACTCTA | 51455 |
| rs190995241 | snp | C/G/T | 3.29594e-05 | 0.00405941 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402969 | CACAGGCCCCTGGCA[C/G/T]AGTTTTTGCAGGACT | 51455 |
| rs191034139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423853 | ATCCTTCATCTATCT[G/T]GCTCCATGGGAAGAA | 51455 |
| rs191065995 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99401971 | CAGGCTGGTCTCAAA[C/T]GATCCACCCACCCCA | 51455 |
| rs191101437 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | REV1 | GRCh38.p7 | 2:99444051 | GGTCTCGATCTCCTG[A/G]CCTCGTGATCCACCC | 51455 |
| rs191111797 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | REV1 | GRCh38.p7 | 2:99479314 | CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 51455 |
| rs191227793 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99408941 | TAAATTGAATTGGAT[G/T]TTCCCATAGAAATGT | 51455 |
| rs191256796 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99468293 | CTGTAATAACATCCA[A/G]GGAAAAGTTCTCCAC | 51455 |
| rs191272973 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99449690 | TTGCTTTTAGTACAT[A/C]CCCCTTCCCTGGCTG | 51455 |
| rs191329912 | snp | A/C | 0.00115455 | 0.0239988 | intron-variant | REV1 | GRCh38.p7 | 2:99407996 | GAGATACATTACACA[A/C]AGTCAGAATTTACAA | 51455 |
| rs191350374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484205 | CAAAGAAGGGAGCAA[C/T]AGACACTGAGTCTAC | 51455 |
| rs191352138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99448923 | CAACATGAGCTTAAA[C/T]GGTAGTGTTGTTTAA | 51455 |
| rs191403295 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99470458 | AAATTTATTCAAAGA[A/C]CTGTGCTAACATTCT | 51455 |
| rs191554743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99428175 | GAGCTCGCATTTTAC[C/T]AACTAGCGAAATTCA | 51455 |
| rs191566290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99431561 | TAACCATGAGTTATG[C/T]CTTACAAGTTGGAGA | 51455 |
| rs191572878 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468105 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 51455 |
| rs191582822 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99435200 | GTTTTAACACAGCAG[A/C]TTCTGTGCCATAGTG | 51455 |
| rs191602389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414919 | GTATACCACAACAAA[G/T]TATGCACTACAGGTG | 51455 |
| rs191606678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99473232 | TATTAGCTGGGAGTG[A/G]TGGCGCATGCCTGTA | 51455 |
| rs191618468 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99455176 | TTGACTGTGCTATAT[A/C]AATCACAGAAAGAAG | 51455 |
| rs191625479 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491895 | AGTAAAATGGTATTA[A/T]CTGCAAACTAGTAGG | 51455 |
| rs191641933 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488651 | TACGCAGCACTGGTC[C/T]CTGCACGGGCAAACC | 51455 |
| rs191648338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453432 | TTTCTTACCCCAAAC[C/T]GGGAAGCAAGAAGGA | 51455 |
| rs191817329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411699 | CAGGTGTGAGCCACC[A/G]CATAGGGCCCCTTTC | 51455 |
| rs191845465 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99441063 | CACAAAGAAGATTTT[G/T]AAAAAACATATCTAT | 51455 |
| rs191855469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418112 | CGGACATACTTTTAT[C/T]AGGCTTAAAAATAGG | 51455 |
| rs191858926 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99476630 | GCTTTGAGCCACTCC[A/T]GATAGTTTTGCACTG | 51455 |
| rs191871605 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | REV1 | GRCh38.p7 | 2:99459101 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51455 |
| rs191952451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407788 | CATGTATATTAGCCC[C/G]TGGTTAATCAGGGGT | 51455 |
| rs192062903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410971 | ACATGTTGGTTACTC[A/G]CTATCACGCTCAGCA | 51455 |
| rs192067600 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | REV1 | GRCh38.p7 | 2:99444111 | AGGTGTGAGCCACCG[C/T]GCCCAGCCCTTTTCT | 51455 |
| rs192088760 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99479566 | GCATTTTTGGAGGCC[A/G]AGGTGGGAAGATCTC | 51455 |
| rs192181649 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400440 | GTCAGTGTGGGGTGT[G/T]TGTTTGAGGAAAAAG | 51455 |
| rs192188491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417845 | TATATAAAACTTCAG[C/T]AAGATTTCTTATTAA | 51455 |
| rs192191722 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99476257 | GGGAGGTAACCTCTA[A/C]GCCCTTAGAACGTCC | 51455 |
| rs192197723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476857 | ACCGTCCATAACTTC[A/G]CTGGCAGAGGATAAC | 51455 |
| rs192395397 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425514 | ACCTTGCACTTGCCT[A/G]GAAAAGGATGACCTA | 51455 |
| rs192440499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99450880 | CAAGTGCTTAACACA[C/T]GTTACTAGCAGCTAC | 51455 |
| rs192447486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99468748 | ATTAGTTTAAAAAAC[A/G]GATGAAGAGTGAATA | 51455 |
| rs192467411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99484939 | ATGGTGCCAACCTTA[C/T]ACGGTAGCTGTAGAT | 51455 |
| rs192469944 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99463612 | TACAAATTTGACAAG[C/T]GGTCTCAGAGCATAT | 51455 |
| rs192549626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99419683 | GAACTGAGGGTAGAA[C/G]AGTCCTCAAAACACA | 51455 |
| rs192589003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484318 | ATCTGTACAACAAAC[A/C]CCCATGACACTAGTT | 51455 |
| rs192597825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459940 | AAAGGAATCAAGAAC[A/G]CTTGGATTATTACAG | 51455 |
| rs192641349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405021 | AAATTAGATCCCACC[C/T]CAGGGAGGGGTGAAG | 51455 |
| rs192641571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454320 | TTTGGTAGGCCACAG[C/T]GGGTGGATCCTCTGA | 51455 |
| rs192645110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464555 | CCAGGTTGAGATATA[C/T]AAAGCTGAATAATGA | 51455 |
| rs192652019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426204 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCACAC | 51455 |
| rs192659040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471530 | CAATGACTTTTTGGG[A/G]AAAATGTAACAGAAA | 51455 |
| rs192676441 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99465990 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCGCA | 51455 |
| rs192680237 | snp | C/T | | | upstream-variant-2KB, intron-variant | REV1 | GRCh38.p7 | 2:99490095 | GCTCCCCGGCCCCGC[C/T]CGCGCTCACAGCCGC | 51455 |
| rs192698228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445613 | TTCTCATCTATTCCA[C/T]ATTTCAAATTTCAAG | 51455 |
| rs192705913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485904 | GAGGATGAGGCAGGA[C/G]ACTGTAGCCCAAGAG | 51455 |
| rs192764384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404111 | CATTGAAACAGGGAC[G/T]CAGGTTGTTACTGTC | 51455 |
| rs192794263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451889 | AGGGACCACTTTGTC[A/G]GGTCCAACAGGCTGG | 51455 |
| rs192827345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99434127 | AGCAAATCAATCATA[C/T]CTTGTAAAACATTCT | 51455 |
| rs192832342 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99471904 | TAAAAAAAAAAAAAA[A/C]AAAAAAACAAGTGTT | 51455 |
| rs192870022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445035 | AAGAGTTTACATTCT[A/C]TACAACGAATCAAAA | 51455 |
| rs192872218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480498 | TTAAGCAAGTGTAAA[C/T]TGGGTGGGAGAGTTT | 51455 |
| rs192920190 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99469499 | AGCCATGTCCAGTCC[A/C]CAGTGCTAACATGCA | 51455 |
| rs192945209 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | REV1 | GRCh38.p7 | 2:99459013 | GGAGATCAAGACCAT[A/C]CTGGCTAACACGGTG | 51455 |
| rs193027923 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99454660 | TGAGGCAGGAAGATC[A/C]GTTGAGCTCAGGAGT | 51455 |
| rs193030011 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99414008 | ATAGAAAAAAGAATT[A/C]GCTGGGTGTGGTGGT | 51455 |
| rs193046586 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490605 | GAACTGACATTTTCC[C/T]ATGTCCAGAGCAACC | 51455 |
| rs193060721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99428735 | GCACAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 51455 |
| rs193134249 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412914 | ACAAGTTTTAATTCC[C/T]AAAGATGCCAACTTA | 51455 |
| rs193149553 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481211 | CCAAATAACTAATGA[A/C]TAATTACGTACATCT | 51455 |
| rs193176147 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99409169 | ACTATTTGAGATACA[C/T]GTGTATCATAACAGG | 51455 |
| rs193295570 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433120 | GTACTTCCTTAAGCT[A/G]TTTCTTATTTTCTAG | 51455 |
| rs199525904 | snp | A/C/G | 9.59057e-05 | 0.00692423 | intron-variant | REV1 | GRCh38.p7 | 2:99449550 | GTCTTATGTGTAAGA[A/C/G]GTAGAACCCTAATGA | 51455 |
| rs199560848 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99488759 | AAGAACCAAGGTTAT[C/G]GTTGGTCCTACCCTA | 51455 |
| rs199566286 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481708 | CACACACACACACAC[-/AA]AAAAATTTAAATTAG | 51455 |
| rs199588746 | in-del | -/TTTCT | 0.0123036 | 0.0774623 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491280 | AAATTGCGTAATTGC[-/TTTCT]TTTCTTTTCTTTTCT | 51455 |
| rs199667839 | snp | A/C | | | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479799 | ATAATAATAATAATA[A/C]TAATACAAGATCCTG | 51455 |
| rs199671405 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99409861 | CAAACAACCCCCCCC[-/A]CCCCCCAAAAAAAAC | 51455 |
| rs199687154 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401222 | AGCTATCAGAGAGCA[G/T]CAGGCTCTCTGGTAA | 51455 |
| rs199701089 | snp | C/T | 0.00018591 | 0.00963952 | intron-variant | REV1 | GRCh38.p7 | 2:99429831 | TTGTAACACACAACT[C/T]CTACATACCTGGCCT | 51455 |
| rs199726562 | snp | A/G | 0.00299551 | 0.0385848 | intron-variant, missense, synonymous-codon | REV1 | GRCh38.p7 | 2:99424820 | CTGAAGTGGCTCCAC[A/G]GTGGTTGAGATGCCA | 51455 |
| rs199726622 | snp | C/T | 9.8912e-05 | 0.0070318 | intron-variant | REV1 | GRCh38.p7 | 2:99464991 | GGTGGAGCTTCTGTA[C/T]TGGGGAGGAAAAAAA | 51455 |
| rs199738055 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99445131 | CTCTGCGTTTAGGAA[A/C]AAAAAAAAAAAACAC | 51455 |
| rs199800438 | in-del | -/CT | 0.0170251 | 0.090679 | intron-variant | REV1 | GRCh38.p7 | 2:99475678 | GGTGACAAAGCAACA[-/CT]CTGTCTCAAAAAAAA | 51455 |
| rs199821990 | in-del | -/A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409862 | AAACAACCCCCCCCC[-/A/G]CCCCCAAAAAAAACA | 51455 |
| rs199850949 | snp | A/G | 0.00130444 | 0.0255052 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405944 | TCTATACTCAGGTTA[A/G]GTCTCGACTGCACAC | 51455 |
| rs199864152 | snp | A/C/G | 1.70507e-05 | 0.00291977 | intron-variant | REV1 | GRCh38.p7 | 2:99434305 | ATCCACAGGAGCACT[A/C/G]AGACTTCAAAGAGAG | 51455 |
| rs199866273 | in-del | -/AG | 0.0103295 | 0.0711199 | intron-variant | REV1 | GRCh38.p7 | 2:99408327 | GCAACCAAGGGGGAA[-/AG]AAAAATTATGGAACA | 51455 |
| rs199901052 | snp | A/G | 1.75736e-05 | 0.0029642 | intron-variant | REV1 | GRCh38.p7 | 2:99407980 | CAAGCCTCAAAAATG[A/G]GAGATACATTACACA | 51455 |
| rs199902703 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405949 | ACTCAGGTTAAGTCT[C/T]GACTGCACACTGACA | 51455 |
| rs199919186 | in-del | -/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432328 | ACATTAGAACTGATC[-/T]TTTTTTTTTTCAAAG | 51455 |
| rs199966978 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99471140 | TAGGCAAGGTTGAAA[A/C]ACAATTTGCCTTTGG | 51455 |
| rs199970240 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99405214 | AATCCACTGTTCCTT[G/T]GCCAGGGCCTACCTG | 51455 |
| rs199998707 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99416944 | AAAAAGAAATAAAGT[A/C]TTTCCAGCCAGGAAG | 51455 |
| rs200032636 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482075 | CCAACCATGTGAATA[C/G]TGGGTTGGGCTTTGA | 51455 |
| rs200037813 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434365 | TTTTATTCTGGTAAT[A/C]CTGCCACTCCAGCTG | 51455 |
| rs200143519 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438799 | AAGGTTTGGATGGCA[C/G]TGAAGGTGCTGCCTT | 51455 |
| rs200169633 | snp | A/T | 0.000332176 | 0.0128832 | intron-variant | REV1 | GRCh38.p7 | 2:99424285 | TGCCAAGTTGCCTAG[A/T]GCGAGAACAAAACAC | 51455 |
| rs200184935 | snp | G/T | 0.000428753 | 0.0146353 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435936 | AATTCAATACTGACA[G/T]ATCTCCTAGAAGGAA | 51455 |
| rs200219079 | in-del | -/A | 0.000661178 | 0.0181701 | intron-variant | REV1 | GRCh38.p7 | 2:99429958 | ATCTGCTTTAAAAAT[-/A]AAAAAAAAATTAATG | 51455 |
| rs200221469 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418188 | AACTTTCACTATAAA[-/T]GAAGATGGAAGACTT | 51455 |
| rs200256755 | snp | C/T | 6.14156e-05 | 0.00554112 | intron-variant | REV1 | GRCh38.p7 | 2:99449291 | TAAATAAAAAGTATT[C/T]TAACTTTAAAAATTT | 51455 |
| rs200265588 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99436740 | CAGAGCTTTCCTCTA[-/TT]ATCAGTCTCATCCTT | 51455 |
| rs200302906 | in-del | -/ACT | | | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402601 | TCAAATCATGAGACG[-/ACT]ACATCTCAGCCTTGG | 51455 |
| rs200429376 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99446295 | ACAAAATGAGGCCCA[C/T]AGGATATATAATCAT | 51455 |
| rs200483066 | snp | G/T | 0.000428202 | 0.0146259 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404515 | GAGGTTCTGGTATTT[G/T]CAACAAGACTGTCCC | 51455 |
| rs200522689 | snp | A/T | 0.00199798 | 0.0315436 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402899 | ATTACCAGGGGTTTC[A/T]CTGCAGGAGGTCCTT | 51455 |
| rs200533023 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99468181 | GCGAAACTCCATCTC[-/AA]AAAAAAAAAAAAGAA | 51455 |
| rs200535277 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444580 | AATTAGACAGCCAAT[A/T]TAAATACTGCAAGTC | 51455 |
| rs200575891 | in-del | -/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491794 | TTCAAACCGAAGATC[-/T]TTTTTTTTTCTTCTT | 51455 |
| rs200602854 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447717 | AGTGACTGCATAAAG[-/T]TTTTTTTTTTTTTCT | 51455 |
| rs200611207 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401055 | GCTACAGTAAAATAA[A/T]TAACACAATTATTTA | 51455 |
| rs200618683 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99452443 | AAAAAAAAAGGAAAA[A/G]AAAAAAAAAGGGGGA | 51455 |
| rs200711316 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439802 | ACAAATAACTTTCAT[-/A]AAAAATGGATTTAAA | 51455 |
| rs200713416 | snp | C/G | 2.14507e-05 | 0.00327489 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403077 | TTTCTTTCACTGCTG[C/G]CTTTAGATGAAGTAA | 51455 |
| rs200733171 | in-del | -/A | 0.0261651 | 0.111346 | intron-variant | REV1 | GRCh38.p7 | 2:99464999 | TCTGTATTGGGGAGG[-/A]AAAAAAAAAATGTCA | 51455 |
| rs200780036 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410732 | CATGGCCTCCAAATT[C/T]TGCAGTTTCTACAGG | 51455 |
| rs200821323 | snp | C/T | 0.0011262 | 0.0237029 | intron-variant | REV1 | GRCh38.p7 | 2:99424904 | CTTTGAGGGACCTAA[C/T]TGAAAATGGTAAATT | 51455 |
| rs200862651 | snp | A/C/G | 4.94681e-05 | 0.00497313 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434381 | CTGCCACTCCAGCTG[A/C/G]GGGTTAGCGCCAGGA | 51455 |
| rs200885876 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99447717 | GTGACTGCATAAAGT[-/C]TTTTTTTTTTTTTCT | 51455 |
| rs200916350 | in-del | -/CA | | | intron-variant | REV1 | GRCh38.p7 | 2:99471142 | TAGGCAAGGTTGAAA[-/CA]CAATTTGCCTTTGGT | 51455 |
| rs201028023 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440975 | AAATATCACGGGTAG[A/G]GATACATTTTTTAGG | 51455 |
| rs201134780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99406517 | AATAAAGAGTATGCT[G/T]CTAGGAAAACTAAAG | 51455 |
| rs201202038 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461024 | TAAGAAGCAATGCCT[A/G]TTTTCATTAACGTTT | 51455 |
| rs201251300 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99426348 | GCGAAATTCTATCTC[-/A]AAAAAAAAAAAAAAA | 51455 |
| rs201259509 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481661 | GAGGCCAGGAGTCTG[-/A]AAACCAGCCTGGGCA | 51455 |
| rs201279451 | snp | G/T | 0.000510561 | 0.0159693 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404576 | GCCATTTACTGGTTC[G/T]TTCTTTTTGTCGCCA | 51455 |
| rs201286407 | snp | A/C | 0.498945 | 0.022939 | intron-variant | REV1 | GRCh38.p7 | 2:99409867 | AACCCCCCCCCCCCC[A/C]AAAAAAAACAGCGTT | 51455 |
| rs201288722 | snp | A/C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99434035 | GTGATACAATAACCA[A/C/G]TAATTAACTCTCACA | 51455 |
| rs201293631 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99477081 | GAGGGTGGTCTTGGG[A/C]CCCCAACTCCACGAT | 51455 |
| rs201333281 | in-del | -/AGG | 0.0267878 | 0.112589 | intron-variant | REV1 | GRCh38.p7 | 2:99407458 | TCGGGAGGCTGAAGA[-/AGG]AGAATTGCTTGAACC | 51455 |
| rs201369748 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484036 | AAATTTATGTAAAAA[A/C]ATCCCACCTATGTGT | 51455 |
| rs201392191 | in-del | -/TCA | | | intron-variant | REV1 | GRCh38.p7 | 2:99421295 | GAATAAGTAAGAAAT[-/TCA]ATTCTAACTTATTTA | 51455 |
| rs201422040 | snp | A/T | 0.000796998 | 0.0199465 | intron-variant | REV1 | GRCh38.p7 | 2:99418811 | AATAAAAGTATTGTT[A/T]AAATATTTCTATTTA | 51455 |
| rs201449155 | in-del | -/AG | 0.0166325 | 0.0896639 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491119 | GTTTACTAGCAACAC[-/AG]AGAATACTCAAATAG | 51455 |
| rs201461170 | snp | C/G/T | 3.30383e-05 | 0.00406427 | intron-variant | REV1 | GRCh38.p7 | 2:99402833 | GATAAAATTGCTATA[C/G/T]TCACACATTATCCAG | 51455 |
| rs201470289 | snp | C/T | 4.95217e-05 | 0.00497578 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439058 | AAAGGCTGGAGAAAG[C/T]CTGCTGGCAACACTG | 51455 |
| rs201539173 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99414457 | CCGAGTTAACAATTT[-/A]AAAAAAAAAAAAAAT | 51455 |
| rs201548583 | in-del | -/CA | 0.0225915 | 0.103853 | intron-variant | REV1 | GRCh38.p7 | 2:99418980 | CATCCAAGAAATAGT[-/CA]CAATTATTTTTTAAA | 51455 |
| rs201585307 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447299 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 51455 |
| rs201595543 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99412074 | ACGTCTCTACTAAAA[A/G]TACAAAAAATTAGCC | 51455 |
| rs201604983 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99454560 | CAGCTCAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 51455 |
| rs201634760 | snp | A/C | 0.0239618 | 0.106802 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434433 | CCTCTGTTACTTGTA[A/C]CAGCCACTGGTTTTC | 51455 |
| rs201658669 | in-del | -/A | 0.485187 | 0.0847778 | intron-variant | REV1 | GRCh38.p7 | 2:99459208 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAGAA | 51455 |
| rs201673753 | in-del | -/C | 0.275999 | 0.248644 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484036 | AAATTTATGTAAAAA[-/C]ATCCCACCTATGTGT | 51455 |
| rs201709236 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99412102 | GCCGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC | 51455 |
| rs201712908 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99404911 | GAAGTGTATATATAC[C/T]ACCAGCCACTATCAC | 51455 |
| rs201747869 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99445202 | TCAACTTTTATTTAA[A/G]TGAGTTGCATAAGCA | 51455 |
| rs201758658 | snp | A/G | 0.000101411 | 0.00712007 | intron-variant | REV1 | GRCh38.p7 | 2:99434320 | AAGACTTCAAAGAGA[A/G]CTCATTTGTACCTGC | 51455 |
| rs201771253 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | REV1 | GRCh38.p7 | 2:99479298 | GCTACTGCACTCCAG[-/A]CCTGGGTGACAGAGC | 51455 |
| rs202090334 | snp | A/G | 6.85178e-05 | 0.00585271 | intron-variant | REV1 | GRCh38.p7 | 2:99410882 | GCTATGGAAAGACAA[A/G]CGTGGAGAAACTACC | 51455 |
| rs202099978 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99433965 | AAAGTTCTACTGTTT[G/T]TTATTCTACTTCCTC | 51455 |
| rs202111573 | in-del | -/AA | 0.0166325 | 0.0896639 | intron-variant | REV1 | GRCh38.p7 | 2:99427388 | TCACTGATTCCATAT[-/AA]AGTTTGCTCTCTACT | 51455 |
| rs202121589 | snp | C/G | 6.58979e-05 | 0.00573974 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421588 | GTAAGTTTGGTCTCT[C/G]CAAGGATTTCGGTAA | 51455 |
| rs202156661 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99453356 | CAAAAAAAAAAAAAA[-/A]GAATTATGTGTCAGC | 51455 |
| rs202166297 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99451834 | GACCCAAAGTTTCAA[G/T]AAAAACAGACCTGCC | 51455 |
| rs202176815 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | REV1 | GRCh38.p7 | 2:99457479 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 51455 |
| rs202200441 | snp | C/T | 1.71572e-05 | 0.00292888 | intron-variant | REV1 | GRCh38.p7 | 2:99410883 | CTATGGAAAGACAAA[C/T]GTGGAGAAACTACCA | 51455 |
| rs202202463 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99474909 | TCCGTTTCAAAAAAG[-/A]AAAAAAAAAAAGAAG | 51455 |
| rs202217893 | in-del | -/CCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99488317 | ATTTTTTAAAAATTA[-/CCC]TGTTCTACTTGAGAC | 51455 |
| rs367551198 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470576 | TTATACTGGTCCAAG[C/T]AAGCGTTAGGTCATA | 51455 |
| rs367697678 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99434525 | AAAAATTTTTCAAAG[A/G]ATTTTAAAAACATGC | 51455 |
| rs367747320 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99422437 | TTCATAATCCACTTG[A/G]TAATGTAGACTAGGA | 51455 |
| rs367768255 | snp | G/T | 3.3024e-05 | 0.00406336 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410816 | CAGTGGCTTCTAGTC[G/T]TCTTTGAATTTCTTC | 51455 |
| rs367772715 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99455621 | TTCCTCCATCTCTTA[C/T]CTACAAGATGAGAGT | 51455 |
| rs367786277 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489216 | AGCAGCAAGGAAAAA[A/C/T]AAGGGAGCAACAACC | 51455 |
| rs367794598 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439984 | AAAAAGTAAAGCCAT[A/G]TCAATGTGTGGGGGT | 51455 |
| rs367869560 | snp | A/G | 0.000131841 | 0.00811808 | intron-variant | REV1 | GRCh38.p7 | 2:99464913 | TATTTTTACTCTTTT[A/G]AAACACACCCATGTT | 51455 |
| rs367919869 | snp | G/T | 0.000157988 | 0.00888644 | intron-variant | REV1 | GRCh38.p7 | 2:99402199 | CACCCTCAGCCATTG[G/T]GACATGCCATTTTTT | 51455 |
| rs367923205 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421544 | GGTCTTTGATTTCCA[C/T]ACGAACAGCATTTGC | 51455 |
| rs367958499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405044 | GGGTGAAGGCCTGAG[A/G]CACATGTTAAAATTC | 51455 |
| rs367978690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99414374 | ATGAAGGCGTTAAGC[A/G]TGCTCGTTCACAATT | 51455 |
| rs368035045 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432623 | TCAAGTTAAAGTAAG[A/G]GTATAAAATACAAAC | 51455 |
| rs368038844 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99471662 | AATCATATCTGATAA[A/G]GGGTTCATACACTTA | 51455 |
| rs368073401 | snp | C/T | 3.29821e-05 | 0.00406078 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402782 | CTGGCACACCTGAAG[C/T]AGAAGCAGAGAGTTC | 51455 |
| rs368088419 | snp | A/G | 0.000115324 | 0.00759268 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438739 | ACATTGATATGTGAT[A/G]CAGTCTTGAATGAGA | 51455 |
| rs368309442 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460960 | TTTTCTTCCTCCTAT[G/T]TGAATAAGGGTGCTC | 51455 |
| rs368315896 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462558 | GAAGTCCCATCCTTC[C/T]GCATAGCAGCATCTG | 51455 |
| rs368322027 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428806 | CATCCTGGCTAACAC[A/G]GTGAAATCCTGCCTC | 51455 |
| rs368331697 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450217 | ACAGAAAATATCTTA[C/T]ATGTCTTAAATATTG | 51455 |
| rs368333660 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99471040 | AAAGAATATGCAATG[A/G]ATGAATGTGCACATT | 51455 |
| rs368359056 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99470952 | GGAACAAGCATTCCA[-/AA]GAGGTTTATCCTATC | 51455 |
| rs368434155 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99402837 | AAATTGCTATATTCA[C/T]ACATTATCCAGGTAT | 51455 |
| rs368478117 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409033 | GTGGCTCACACCTGT[A/G]ATCCCAAAACGCTGG | 51455 |
| rs368508902 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99413665 | AGCCCCACCTAAAGG[A/C]TACTGATTAATTCTG | 51455 |
| rs368515595 | snp | C/T | 0.00122105 | 0.0246786 | intron-variant | REV1 | GRCh38.p7 | 2:99406147 | GCCTCTTCAGATCAT[C/T]GGGCAGGGCCTTTAA | 51455 |
| rs368535770 | snp | A/G | 6.61868e-05 | 0.00575231 | intron-variant | REV1 | GRCh38.p7 | 2:99421673 | CAACACAGAGCAAAG[A/G]CAACGAATCACAGCC | 51455 |
| rs368609235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99422936 | GATGCTACCACTGAC[C/T]TCCTCCTTTCAAAGA | 51455 |
| rs368626078 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99407994 | GAGAGATACATTACA[C/G]AAAGTCAGAATTTAC | 51455 |
| rs368639067 | snp | A/G | 4.68373e-05 | 0.00483906 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402361 | TCTAGGAAGGGGGAA[A/G]AACTTCAAATGAGGA | 51455 |
| rs368644596 | in-del | -/GTATAGGATGG | | | intron-variant | REV1 | GRCh38.p7 | 2:99425453 | TTAGCGAGGTGCTGG[-/GTATAGGATGG]CAAATAAAGCAAACT | 51455 |
| rs368649373 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99402839 | ATTGCTATATTCACA[C/T]ATTATCCAGGTATAT | 51455 |
| rs368655067 | in-del | -/T | 0.279195 | 0.248289 | intron-variant | REV1 | GRCh38.p7 | 2:99443848 | ACCAACTTTTCTTCC[-/T]TTTTTTTTTTTTGAG | 51455 |
| rs368717842 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99484897 | ACCAGCCAAATAACA[A/C]CACCTCTCTAAATCT | 51455 |
| rs368718842 | snp | C/T | 8.24749e-05 | 0.00642111 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421524 | AGAGGCAGCACATTT[C/T]GTCTGGTCTTTGATT | 51455 |
| rs368737028 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99476286 | CCACCTTATGGGAGC[-/A]GTGACTCACGCCTGT | 51455 |
| rs368768627 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99446828 | GTAAATCAATTCCCC[A/C]CAGCAAGATCGCTTT | 51455 |
| rs368812454 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438821 | TGCTGCCTTGCTAAA[C/G]GTAGATACTGAAGAA | 51455 |
| rs368815341 | snp | A/G/T | 9.43608e-05 | 0.00686823 | synonymous-codon, missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406101 | GATCCACAGCAGCCC[A/G/T]AAATACTACAAAAAG | 51455 |
| rs368905322 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484563 | GAAGCACCAAGACAC[-/AT]GATTCTTTGACTTAT | 51455 |
| rs368959370 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477884 | CTAATGCTTTTCTTC[C/T]CTTCAATTACAGATT | 51455 |
| rs369014279 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472293 | TTATGGTAAGTGAAA[C/T]AAACCATTCACAAAA | 51455 |
| rs369045854 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402994 | AGGACTGTTAAGCAG[C/T]TTGTTATTCAAAGGA | 51455 |
| rs369069898 | in-del | -/TTA | | | intron-variant | REV1 | GRCh38.p7 | 2:99446005 | TATAATAAAATCTCA[-/TTA]AAACACAGCTAAGAA | 51455 |
| rs369098545 | snp | A/C/G | 3.29925e-05 | 0.00406145 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438846 | GAAGAAGTGCTTTTT[A/C/G]TGCTTGAAGGCCCCT | 51455 |
| rs369125032 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452632 | TTCCCCCCTGGAACA[C/T]ATGCTCTTTGAAGGC | 51455 |
| rs369169730 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463098 | ATCTCAAAAAAAAAT[A/T]ATAATAAATAAATAT | 51455 |
| rs369175845 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416976 | AAATGAAGGTGAATG[A/G]TAGGATTACTAGGTC | 51455 |
| rs369179765 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99442525 | GTGACAATGAGCTTC[A/G]TGAAAAATATTCAAT | 51455 |
| rs369207234 | snp | A/G | 1.71469e-05 | 0.002928 | intron-variant | REV1 | GRCh38.p7 | 2:99429825 | TAAGAATTGTAACAC[A/G]CAACTTCTACATACC | 51455 |
| rs369223586 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99409798 | CAATGAGCCGAGATC[A/G]CACCACTGCCCTCAG | 51455 |
| rs369235061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423823 | TAAAAGAGAAAAACC[A/G]GGTTAAAAAATTCCA | 51455 |
| rs369255284 | snp | A/T | 0.000131127 | 0.00809606 | intron-variant | REV1 | GRCh38.p7 | 2:99438555 | ATAAGAGCAAAATGA[A/T]CAAGCATGACTGTTT | 51455 |
| rs369257192 | in-del | -/TGTT | 0.0023933 | 0.0345097 | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400437 | GAAGTCAGTGTGGGG[-/TGTT]TGTTTGAGGAAAAAG | 51455 |
| rs369323449 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401268 | TAATGTGCTTCCATA[A/C]GTTTGTTGTAAAACC | 51455 |
| rs369345409 | snp | A/C | 9.89919e-05 | 0.00703464 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439028 | GCTCTTCTCAGCCTT[A/C]TCCTCCTCCTGGGAA | 51455 |
| rs369368558 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403702 | AGGCTCACCAGATGC[A/G]CTGGCTGACTGCTGG | 51455 |
| rs369464334 | snp | A/G | 3.41384e-05 | 0.00413135 | intron-variant | REV1 | GRCh38.p7 | 2:99434302 | GCCATCCACAGGAGC[A/G]CTAAGACTTCAAAGA | 51455 |
| rs369466561 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99405589 | ACTTCACCACTAATC[-/C]ACCAAAGCTGCCTTG | 51455 |
| rs369541955 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405985 | ATGTAGACCATTCCA[C/T]TTCCCTGAAGACTCA | 51455 |
| rs369614513 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429880 | TTTCAGCCCTTGACA[A/G]AACAGAATCAATTCC | 51455 |
| rs369615712 | snp | C/G/T | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99462673 | TTACATTTTCTCCCC[C/G/T]CTTTTTTGAAAAAAA | 51455 |
| rs369628255 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99451380 | GAAAACTAATTACTC[C/T]AGAAATTTGGAACTG | 51455 |
| rs369653882 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99437126 | CTGAGACCGCAGGTG[A/C]GTGCCACCACGCCCA | 51455 |
| rs369662260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477227 | ACGCTCCTCTCAAAA[C/T]CGGGGGTGGCCATGT | 51455 |
| rs369682349 | snp | A/G | | | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406455 | TGTGGAAGGGTTCAG[A/G]TTAGTTGGAACCAAC | 51455 |
| rs369759841 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436269 | TGCAATCTACAAACG[C/T]GCCTGGATAAAATAA | 51455 |
| rs369759935 | snp | C/T | 4.95323e-05 | 0.00497631 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439150 | CATTAAAAATGGCAG[C/T]GCTCCCTCTGGGATG | 51455 |
| rs369818371 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456072 | TCACTCCCCCTGGGC[A/G]GCTTTCACAAAAATA | 51455 |
| rs369833498 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447476 | CGCCCAGCCAATATA[C/T]TTGACTTTCTAGAGA | 51455 |
| rs369895628 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467855 | GTTGGAGACCAGTCT[A/G]GCCAACATGGTGAAA | 51455 |
| rs369927640 | in-del | -/ATAAAACAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99453922 | AAAAAAAAAATCAAA[-/ATAAAACAAAA]CTAGATTCAGGGAAA | 51455 |
| rs370065152 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99411379 | AAAGTGAAAGTAATG[A/C]GTACTTTTAAAAGAT | 51455 |
| rs370092323 | snp | C/T | 5.0358e-05 | 0.00501761 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401206 | CAAGCACTTATGGCA[C/T]AGCTATCAGAGAGCA | 51455 |
| rs370095772 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490278 | GTGACCGTCTCGCTA[C/G]CTGGGCGGAGGGGAG | 51455 |
| rs370104816 | snp | A/C | 3.3006e-05 | 0.00406226 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424254 | TTAGCATGCCCAAAA[A/C]ACATTCCGTTCTTAA | 51455 |
| rs370130836 | snp | A/G | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421525 | GAGGCAGCACATTTC[A/G]TCTGGTCTTTGATTT | 51455 |
| rs370131174 | in-del | -/CC | | | intron-variant | REV1 | GRCh38.p7 | 2:99442277 | AAAAAAAAAAAAAAA[-/CC]AACCAGCTTTGCAGT | 51455 |
| rs370145088 | snp | A/C | 0.000185391 | 0.00962607 | intron-variant | REV1 | GRCh38.p7 | 2:99403157 | GATAGTATGGATAGT[A/C]TGGATGACAGTATTG | 51455 |
| rs370200291 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406383 | TTGGAAGACATCACG[A/G]ACAGAGTATGACCCA | 51455 |
| rs370293300 | snp | G/T | 0.000155988 | 0.00883005 | intron-variant | REV1 | GRCh38.p7 | 2:99402231 | CCATTTGATAAAAGT[G/T]ATGAATTACTACCTT | 51455 |
| rs370314456 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99448187 | TGTGGAACAGTTAAT[A/G]GAGGGTGTTATAATT | 51455 |
| rs370328392 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487997 | GGAAATGGTATCTTC[A/G]TTCTACAAACGAGAA | 51455 |
| rs370407613 | in-del | -/GAG | | | intron-variant | REV1 | GRCh38.p7 | 2:99458999 | AGATCACGAGGTCAG[-/GAG]ATCAAGACCATACTG | 51455 |
| rs370410916 | snp | C/T | 0.000149488 | 0.00864417 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438628 | CAACAAGTGCAGACC[C/T]GCCTGTTTTCATTTT | 51455 |
| rs370465682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99411849 | TGCCTAAGGAAACAA[A/G]ACTCCTGAGGTCCAC | 51455 |
| rs370507683 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99409854 | TCTCAAAACAAACAA[-/C]CCCCCCCCCCCCCAA | 51455 |
| rs370514211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405478 | TCAAGGACCAGCAGT[A/G]TATCACATGTACAGC | 51455 |
| rs370525776 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428071 | TGGAGGCAGCCCTGC[A/T]CCCCAGCCAGCATTC | 51455 |
| rs370638855 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99426263 | GAGGCAGGAGAATCG[C/T]TTGAACCTGGGAGGT | 51455 |
| rs370656864 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99469703 | CAAGACTACTTATGC[A/G]TGCATTTTTCCTAAT | 51455 |
| rs370657049 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413668 | CCCACCTAAAGGATA[C/T]TGATTAATTCTGTTG | 51455 |
| rs370663666 | in-del | -/TTC | 0.0150606 | 0.0854603 | intron-variant | REV1 | GRCh38.p7 | 2:99403931 | TCTGATCTGTACGAA[-/TTC]TTAACAGTTCCCCAA | 51455 |
| rs370682495 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449470 | TTGACCTCCATGCAA[C/T]ATCATTAGTTTTCTC | 51455 |
| rs370690406 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404514 | TGAGGTTCTGGTATT[C/T]GCAACAAGACTGTCC | 51455 |
| rs370714320 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | REV1 | GRCh38.p7 | 2:99403118 | GGCACTAAGAGCAGA[C/T]GGATATAAGATCCTC | 51455 |
| rs370725674 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | REV1 | GRCh38.p7 | 2:99408625 | TACAGTACAGCCAAT[A/G]AACAATTCTTAGATC | 51455 |
| rs370747224 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99452704 | AGCAGGTGCTCAGTG[A/G]GTATTTGCTAAATTC | 51455 |
| rs370764851 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436990 | CCCAACTTTTTTTTT[-/G]TTTTTTTTTTTTTTT | 51455 |
| rs370835867 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419153 | CTCTTTGCTCTAACG[C/T]AAGTGCCACTTCAGC | 51455 |
| rs370872980 | snp | C/T | | | intron-variant, upstream-variant-2KB, synonymous-codon | REV1 | GRCh38.p7 | 2:99479876 | CATAAATCTCATGTT[C/T]GAGAAGACACCCAAG | 51455 |
| rs370897058 | snp | A/C/G | 3.30334e-05 | 0.00406397 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418830 | TATTTCTATTTACCT[A/C/G]GTAGATTGGTCACTA | 51455 |
| rs370908094 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432010 | TGTTGTTCTTTAGAA[C/T]GAAAACTGAAGTTGT | 51455 |
| rs370916770 | snp | C/T | 0.029116 | 0.117091 | intron-variant | REV1 | GRCh38.p7 | 2:99409760 | AGACAGGAGGATTGC[C/T]TGAACCCAGGAGGTA | 51455 |
| rs370926825 | snp | A/G | 3.29935e-05 | 0.00406149 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418938 | ATTCTAGCCAGGAGA[A/G]TATTAGAACCTATTA | 51455 |
| rs371046946 | snp | C/T | 4.9458e-05 | 0.00497258 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435895 | ATCCATATCAACATG[C/T]ATTATACAGCTCTGA | 51455 |
| rs371052832 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402599 | TCTCAAATCATGAGA[C/T]GACTACATCTCAGCC | 51455 |
| rs371094677 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99474962 | ACTTTGTTGCTAACC[A/G]GTTCTCTGAACTTAA | 51455 |
| rs371250786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99411149 | AAAAATTAGCCTGGC[A/G]TGGTGGCGGGTGCCT | 51455 |
| rs371252747 | in-del | -/CCCCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99421683 | AAAGGCAACGAATCA[-/CCCCC]CAGCCACAGCCACCA | 51455 |
| rs371261199 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455855 | TTCCCCCTTGTTTCA[A/T]TTTGTGAATTGTGCT | 51455 |
| rs371268487 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99476080 | TATTATGCAACTTTA[C/T]GTAACTTTTTCTATG | 51455 |
| rs371311182 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422443 | ATCCACTTGGTAATG[C/T]AGACTAGGAGGGCGG | 51455 |
| rs371321383 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99462835 | GCTCACACCTGTAAT[A/C]CCAGCACTTTGGGAA | 51455 |
| rs371360329 | in-del | -/A | 0.288646 | 0.246995 | intron-variant | REV1 | GRCh38.p7 | 2:99457687 | AGACCCTGTCTCAAG[-/A]AAAAAAAAAAAAAAG | 51455 |
| rs371395259 | snp | A/G | 1.81787e-05 | 0.0030148 | intron-variant | REV1 | GRCh38.p7 | 2:99405880 | TTAGGAGTATAAAAT[A/G]TACTTATATTTAGGA | 51455 |
| rs371442974 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99414720 | CTCTCTTTTGTCCCT[C/T]CCACTATTGCCTCAC | 51455 |
| rs371448600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459168 | AGCCGAGATCGCGCC[A/G]CTGCACTCCAGCCTG | 51455 |
| rs371461236 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481292 | TTATTAAGCTTTAAA[C/G]TATCAAGTATACAGT | 51455 |
| rs371487243 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438867 | GAAGGCCCCTGAACA[A/G]TGGAGTGGTGAGCAC | 51455 |
| rs371631883 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99479232 | ACTTGGGGGCTGAGG[A/C]AGAAGAACTGCTTGA | 51455 |
| rs371688126 | snp | A/G | 0.00011536 | 0.00759387 | intron-variant | REV1 | GRCh38.p7 | 2:99464916 | TTTTACTCTTTTAAA[A/G]CACACCCATGTTTCC | 51455 |
| rs371690018 | snp | C/T | 3.31763e-05 | 0.00407272 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405931 | AGGTGACGGGACCTC[C/T]ATACTCAGGTTAAGT | 51455 |
| rs371702778 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476299 | GCAGTGACTCACGCC[A/T]GTAATCCCAACACTT | 51455 |
| rs371730026 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99434489 | CTGTATGTGGTACAG[C/G]AATGTTAACAACATG | 51455 |
| rs371761779 | snp | A/C | 4.94564e-05 | 0.0049725 | intron-variant | REV1 | GRCh38.p7 | 2:99462638 | TCTGTGCTAGTGAC[A/C] | 51455 |
| rs371764819 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99427054 | CAGGCGTGGTGGCGG[A/G]AGCAGTAATCCCAGC | 51455 |
| rs371779609 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401225 | TATCAGAGAGCATCA[A/G]GCTCTCTGGTAATAT | 51455 |
| rs371863682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481219 | CTAATGAATAATTAC[A/G]TACATCTAAAAGTAC | 51455 |
| rs371871241 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99454383 | TGGAGAAACCCCGTC[A/G]CTACTAAAAATACAA | 51455 |
| rs371883530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99433920 | TATGGAGAATGATTA[C/T]TGGTGTTTACTTTTA | 51455 |
| rs371898747 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403027 | CTGAATCCTTTTTGG[G/T]GAACCAATGGTTTTT | 51455 |
| rs371902874 | snp | A/G | 8.65289e-05 | 0.006577 | intron-variant | REV1 | GRCh38.p7 | 2:99406154 | CAGATCATCGGGCAG[A/G]GCCTTTAATCCTCTG | 51455 |
| rs371935316 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99471816 | AAAAACGTTCAGTGT[C/T]ATTAATCACTATGGA | 51455 |
| rs372080864 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477130 | TCCAGTATTCATTCT[C/T]CTTTCTTACTTTTAG | 51455 |
| rs372122844 | snp | C/T | 4.94222e-05 | 0.00497078 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421579 | TCATCAGGAGTAAGT[C/T]TGGTCTCTGCAAGGA | 51455 |
| rs372140858 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | REV1 | GRCh38.p7 | 2:99488968 | GTGAGAAGACGTGGA[A/G]ATAAAGAGAATTAGC | 51455 |
| rs372220834 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440726 | CAAAGAAATGTACAA[A/C]ATGTACTGAATATAC | 51455 |
| rs372227377 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476028 | GTGTATGATTCTACA[C/T]ATCTAGTTTTAAAAA | 51455 |
| rs372289119 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477154 | CTTTTAGTAATGGAA[C/T]ACCTCTCCCGCCCCT | 51455 |
| rs372314401 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450320 | ACTAAAGTCATATTA[C/T]GGCCTGCATTACTAG | 51455 |
| rs372314961 | snp | A/G | 3.306e-05 | 0.00406558 | intron-variant | REV1 | GRCh38.p7 | 2:99402849 | TCACACATTATCCAG[A/G]TATATTAAGATCTCA | 51455 |
| rs372320838 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99441983 | TTGTGGCCAGGCGTG[A/G]TGGCTCATGCCTGTA | 51455 |
| rs372344352 | snp | A/G | 0.00148158 | 0.0271771 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404593 | TCTTTTTGTCGCCAT[A/G]TGACTCTGCTTGCTG | 51455 |
| rs372345793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482365 | TAATTCCAAGAACAG[C/T]ACTTTCCTGAGGTCT | 51455 |
| rs372367876 | snp | C/T | 4.95479e-05 | 0.0049771 | intron-variant | REV1 | GRCh38.p7 | 2:99402825 | AAACAAAGGATAAAA[C/T]TGCTATATTCACACA | 51455 |
| rs372380799 | snp | A/G | 4.94271e-05 | 0.00497102 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438761 | TGAATGAGAATAGAA[A/G]TTTGAAATAAAATTG | 51455 |
| rs372395154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482932 | TGAGGCAGGACAATC[A/G]CTTGAACCTGGGAGG | 51455 |
| rs372495457 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99455186 | TATATAAATCACAGA[-/AAG]AAGTGAGGTGAATGG | 51455 |
| rs372517401 | snp | A/G | 1.6582e-05 | 0.00287936 | intron-variant | REV1 | GRCh38.p7 | 2:99424130 | AAACACAGACACAAA[A/G]TGACAGTTTGATACA | 51455 |
| rs372529278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99414933 | ATTATGCACTACAGG[C/T]GCAAAGGAAAGGCTA | 51455 |
| rs372532913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423041 | ATAACTGGAAAGTTA[A/T]TTAGTGTGTTCTCTT | 51455 |
| rs372545854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445969 | TTTATTAAATAGCTA[A/T]TACATGTTAAAATTT | 51455 |
| rs372549890 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452847 | AAATTAGAGACGCCA[C/T]ATAATGTATTAAGAG | 51455 |
| rs372558007 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99424998 | ATAATTATGGAATTA[C/T]ACATAATTAGTAAAA | 51455 |
| rs372573851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99467211 | AATTCCTTAATGATG[A/G]TTTAATGAGGCTAGA | 51455 |
| rs372596093 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99465257 | ATTCCTGAGCACCAA[C/T]CCTAACATTCACTTA | 51455 |
| rs372674771 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404583 | ACTGGTTCTTTCTTT[G/T]TGTCGCCATGTGACT | 51455 |
| rs372704853 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99420517 | CTAACAAAGGCTCTG[C/G]AGCCTAGGCGCTCCG | 51455 |
| rs372736402 | snp | A/C | 0.00207576 | 0.0321492 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402362 | CTAGGAAGGGGGAAA[A/C]ACTTCAAATGAGGAC | 51455 |
| rs372793152 | in-del | -/A | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483122 | CAGGTTAAATGCTTT[-/A]AAAAAAAAGGCTTAA | 51455 |
| rs372816301 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415159 | CAGGACCAAAACCTT[C/G]AAGAGGGCTGCTAGT | 51455 |
| rs372862152 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99437076 | CCTCAACCCCTAGGG[C/G]TCAAACAATCCTCCC | 51455 |
| rs372891153 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482190 | CCCATAAAAACTCCA[C/G]ATGCTGTAGAGTAAG | 51455 |
| rs372931071 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477677 | ATATTAAACCTGAAA[A/G]TGTATAACAAACATT | 51455 |
| rs372932712 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99401364 | CAGCCTAAAGGTGGG[G/T]AGAGAAGAAATGTCA | 51455 |
| rs372997350 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486223 | TTCAAATAGTTCCTA[C/G]AAGGTTTAAAATTTC | 51455 |
| rs373000879 | snp | C/T | 8.25457e-05 | 0.00642386 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439081 | CAACACTGTTGACCA[C/T]GGGCACCAAGCAATC | 51455 |
| rs373008850 | snp | G/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403717 | GCTGGCTGACTGCTG[G/T]TGAGTGCTGTTCTCG | 51455 |
| rs373024038 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447440 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 51455 |
| rs373052815 | snp | C/G | 3.56907e-05 | 0.00422422 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406459 | GAAGGGTTCAGATTA[C/G]TTGGAACCAACTGAT | 51455 |
| rs373101258 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472944 | GTTTTGATTCAACCT[C/T]ACAGACCATCATTGT | 51455 |
| rs373132107 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99416912 | AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 51455 |
| rs373157507 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419964 | TAGTGAGTTCAGGGG[-/G]AGGGGAAAGGCACTG | 51455 |
| rs373172649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99447322 | GGACTACAGGCGCGC[A/G]CCACCACGCCCAGCT | 51455 |
| rs373197849 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436129 | TTAATTAAGTCTCTA[A/G]TTAGTCAAAAAGTGC | 51455 |
| rs373211992 | snp | A/G | 0.00158497 | 0.0281064 | intron-variant | REV1 | GRCh38.p7 | 2:99401370 | AAAGGTGGGGAGAGA[A/G]GAAATGTCATTAGGA | 51455 |
| rs373313528 | in-del | -/CTCCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99404306 | GGAGACAAGCCCACT[-/CTCCC]CTCCCCTCCCCTCCC | 51455 |
| rs373343985 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467108 | ATAAAGGAGTAAAGT[A/G]TATTTTAATACATTT | 51455 |
| rs373375723 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412921 | TTAATTCCCAAAGAT[A/G]CCAACTTAGATTCCA | 51455 |
| rs373394752 | snp | C/T | 1.68049e-05 | 0.00289865 | intron-variant | REV1 | GRCh38.p7 | 2:99429835 | AACACACAACTTCTA[C/T]ATACCTGGCCTCATA | 51455 |
| rs373464759 | snp | A/G | 0.000126025 | 0.00793704 | intron-variant | REV1 | GRCh38.p7 | 2:99403830 | CCTAGTGGAAAAGAC[A/G]AGGTCAAAGTCAAAC | 51455 |
| rs373480147 | snp | A/G/T | 3.86033e-05 | 0.0043932 | intron-variant | REV1 | GRCh38.p7 | 2:99403123 | TAAGAGCAGATGGAT[A/G/T]TAAGATCCTCAACAA | 51455 |
| rs373482406 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99443920 | CGATCTCGGCTTCAC[C/G]CCATTCTCCTGCCTC | 51455 |
| rs373484267 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99429681 | TTATCTAGCACTGGT[A/G]GGGGGTTGTGGGGGG | 51455 |
| rs373489351 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99451176 | TTAATATGGGCACCA[A/G]ATCCAATGAAATCAC | 51455 |
| rs373493694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458118 | ATCTCATCAAAATTA[A/C]AAACGTTCTGCAAAA | 51455 |
| rs373495016 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99484953 | ATACGGTAGCTGTAG[A/G]TATTAATTAAGACAC | 51455 |
| rs373499374 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472385 | AAAGCAGAATGGTGG[C/T]TGCGGGTGGAGTTAC | 51455 |
| rs373551520 | snp | A/G | 5.09022e-05 | 0.00504465 | intron-variant | REV1 | GRCh38.p7 | 2:99438589 | AAGAAGACAATTTTA[A/G]TAAGTATCTACCTGT | 51455 |
| rs373594395 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407445 | TACCCCCAGCTACTC[A/G]GGAGGCTGAAGAAGG | 51455 |
| rs373600558 | snp | C/T | 0.0113303 | 0.0744095 | intron-variant | REV1 | GRCh38.p7 | 2:99451531 | AGATCACATAAACTA[C/T]GGAATAAGACCGATC | 51455 |
| rs373644274 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99473850 | GTAAGTATGATCTTT[C/T]CATCTTTTCTTGGGA | 51455 |
| rs373645542 | snp | C/T | 5.25597e-05 | 0.00512612 | intron-variant | REV1 | GRCh38.p7 | 2:99429978 | AAAAATTAATGGTTA[C/T]ATGTTATAAACTGAT | 51455 |
| rs373651460 | snp | C/G/T | 6.6755e-05 | 0.00577699 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408046 | CTCTCATATCTGATA[C/G/T]ATTTAGTTTCATTGT | 51455 |
| rs373653063 | in-del | -/TAAAAG | | | intron-variant | REV1 | GRCh38.p7 | 2:99454872 | AAAGCACAGTAAAAG[-/TAAAAG]CCATATACAAGGACC | 51455 |
| rs373660388 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472710 | TTTTTACTTTGAATT[G/T]GCAGTAGTGGGAGGC | 51455 |
| rs373669397 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99428072 | GGAGGCAGCCCTGCT[A/C]CCCAGCCAGCATTCA | 51455 |
| rs373713332 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414824 | AAGATTAGCAAGAGA[C/G]AATCATCATCCTGGG | 51455 |
| rs373741843 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449350 | CCTTTCCACAATCCA[C/T]TCTGGTCGAATTACT | 51455 |
| rs373824185 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442358 | ATTGCTTGGACCTGG[C/T]AGAGGATCCTCAGGT | 51455 |
| rs373840536 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421536 | TTTCGTCTGGTCTTT[A/G]ATTTCCATACGAACA | 51455 |
| rs373850478 | in-del | -/AAAAAAA | 0.5 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99454551 | GTGAAACTCCAGCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs373851354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421910 | AAATAACCAACAAAA[A/G]AAATTTAAACACAAA | 51455 |
| rs373851872 | snp | A/T | 0.000241633 | 0.010989 | intron-variant | REV1 | GRCh38.p7 | 2:99406504 | ACCTAGAACCCAGAA[A/T]AAAGAGTATGCTTCT | 51455 |
| rs373913101 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464343 | ATTAAAATATTATAT[A/G]CTCACTATGAAGTTT | 51455 |
| rs373922489 | snp | A/G/T | 3.29594e-05 | 0.00405941 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402739 | GGTCTCACACAGCCA[A/G/T]CTGGGTCAGACTGCA | 51455 |
| rs373944204 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439977 | AATAGACAAAAAGTA[A/G]AGCCATGTCAATGTG | 51455 |
| rs373974745 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99479326 | AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 51455 |
| rs373976399 | snp | G/T | 4.97409e-05 | 0.00498678 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439270 | TCATGCCATTGACTT[G/T]GACTTCATTTTCCGT | 51455 |
| rs373986919 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99462274 | TTTCATTTTAAACCT[C/T]ACGTGACTTTTTGAA | 51455 |
| rs374004177 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99438541 | ATACCAATAATAGCA[C/T]AAGAGCAAAATGATC | 51455 |
| rs374073679 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99414318 | TCAATGTGGGTCAGA[A/C]AAGTTTAAACCCAGA | 51455 |
| rs374078558 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480239 | GGGATGGGAGAACTG[C/G]TTGAGCCTGGGAGGT | 51455 |
| rs374111453 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402663 | AATTGTAGTTATCCA[C/T]TCTCTGAGCAAGGTC | 51455 |
| rs374206477 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99421666 | TAGCTATCAACACAG[A/G]GCAAAGGCAACGAAT | 51455 |
| rs374255141 | snp | C/T | 8.2763e-05 | 0.00643231 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439263 | CAACTGTTCATGCCA[C/T]TGACTTTGACTTCAT | 51455 |
| rs374260652 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99431267 | ATCCTACTTGCTTCA[A/C]AACAGCAGAGTGTGT | 51455 |
| rs374263636 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419675 | AGCAGTGGGAACTGA[A/G]GGTAGAAGAGTCCTC | 51455 |
| rs374280450 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99448971 | TGTCAATCAGGAGGC[A/G]ATATATTAGTTACAA | 51455 |
| rs374281024 | snp | A/C | 4.71509e-05 | 0.00485523 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402359 | GATCTAGGAAGGGGG[A/C]AAAACTTCAAATGAG | 51455 |
| rs374320014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448243 | ATTCAGCAACTGACT[C/T]AAAAAGATAAGCAAT | 51455 |
| rs374363952 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99452442 | AAAAAAAAAGGAAAA[-/G]GAAAAAAAAAGGGGG | 51455 |
| rs374431846 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413307 | TGTCATTTAAACAAG[C/T]CTATAGTGTGACTTA | 51455 |
| rs374443198 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99441738 | TCATAAAAATCCATG[A/G]AAAAACTTATTAACA | 51455 |
| rs374445801 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99458935 | GTGTGGAGGCCGGGC[A/G]CGGTGGCTCACACCT | 51455 |
| rs374500583 | snp | A/G | 0.000401543 | 0.0141637 | intron-variant | REV1 | GRCh38.p7 | 2:99418987 | GAAATAGTCACAATT[A/G]TTTTTTAAATTTCTC | 51455 |
| rs374502768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444441 | CAGACTCTACAGGTA[C/T]TCTCTATGGTCAGCA | 51455 |
| rs374541203 | snp | A/G/T | 4.97206e-05 | 0.0049858 | intron-variant | REV1 | GRCh38.p7 | 2:99404687 | ATCCAGCTATAAAAT[A/G/T]CCAAACATATGAGTA | 51455 |
| rs374544002 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99479281 | GCAGTCAGCCGAGAT[G/T]AGGCTACTGCACTCC | 51455 |
| rs374589982 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99446863 | TCAACTCTCCTCCTG[A/T]CCACAGAAATTCCCC | 51455 |
| rs374612753 | snp | C/G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475649 | CCGAGATTGAGCCAC[C/G/T]GTACTACAGCTTGGG | 51455 |
| rs374695385 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99445449 | AATATAAAAAACCCA[C/T]GCTACAAGGTTCTCA | 51455 |
| rs374710192 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488292 | AGTGATCTTATATAT[G/T]CAAGCACATTATTTT | 51455 |
| rs374819675 | snp | A/G/T | 3.29713e-05 | 0.00406015 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438815 | TGAAGGTGCTGCCTT[A/G/T]CTAAACGTAGATACT | 51455 |
| rs374841462 | in-del | -/TA | | | intron-variant | REV1 | GRCh38.p7 | 2:99408610 | CCTTTCATTGTGTTT[-/TA]ACAGTACAGCCAATA | 51455 |
| rs374846518 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99426737 | GTGACTCATCTATTA[C/G/T]AACTAAAATCCCATA | 51455 |
| rs374888832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99459025 | CATACTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 51455 |
| rs374904598 | snp | A/C | 1.64754e-05 | 0.00287009 | splice-donor-variant | REV1 | GRCh38.p7 | 2:99403694 | CACTTCCAAGGCTCA[A/C]CAGATGCGCTGGCTG | 51455 |
| rs374958831 | snp | A/G | 0.00116995 | 0.0241579 | intron-variant | REV1 | GRCh38.p7 | 2:99464872 | ATAACAGAAGAATGA[A/G]AAATAACTAGACAGT | 51455 |
| rs375052223 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480272 | GACTGTAGTGAGCCA[-/A]TCATCACGTCACTGC | 51455 |
| rs375090189 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405935 | GACGGGACCTCTATA[C/T]TCAGGTTAAGTCTCG | 51455 |
| rs375135814 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99409887 | AAAACAGCGTTTTTA[A/C]ATGCTTTTACCAGTT | 51455 |
| rs375163084 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99455580 | GCATAAATTAATATG[C/G]TAAGTCTTCTATGTC | 51455 |
| rs375180479 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419237 | TTTTTTGGGGGATGG[A/G]GGCTCACTCTGTTGC | 51455 |
| rs375199587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489090 | AGAGCAGCGAAACAC[A/G]GCGCGGCTCGGTGCG | 51455 |
| rs375344645 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99451284 | CGGCTGTCCTTTACC[A/G]AATAAAAAGACACGT | 51455 |
| rs375371261 | snp | C/T | 7.02494e-05 | 0.00592619 | intron-variant | REV1 | GRCh38.p7 | 2:99407987 | CAAAAATGAGAGATA[C/T]ATTACACAAAGTCAG | 51455 |
| rs375414036 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99478889 | ACCTAAAAATGTATC[C/T]ATAGTGGTGATAATA | 51455 |
| rs375476190 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462507 | CAACCTGTGTATCCA[C/T]TAACATAGATGGCAA | 51455 |
| rs375499981 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414948 | TGCAAAGGAAAGGCT[A/G]TATTAAACATCACCA | 51455 |
| rs375510150 | snp | A/G | 0.000166023 | 0.00910954 | intron-variant | REV1 | GRCh38.p7 | 2:99405876 | ATATTTAGGAGTATA[A/G]AATGTACTTATATTT | 51455 |
| rs375524445 | in-del | -/GT | | | intron-variant | REV1 | GRCh38.p7 | 2:99429243 | GATATATATATATGA[-/GT]GTGTGTGTGTTTCTT | 51455 |
| rs375533394 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99455954 | CTGGTCTTTTACCCA[C/T]GTACTAAAGGAAGTA | 51455 |
| rs375545454 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432539 | GATAATCTATTCATT[G/T]TATATGTAGCAAATA | 51455 |
| rs375569840 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477197 | CAGAGTGGGCAACCA[A/G]AGACTACATTTCCCA | 51455 |
| rs375629417 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99401899 | GGGCACCACCACCCC[-/G]CCCAGATTATTTATT | 51455 |
| rs375675652 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487050 | GGCGATGACATTTGA[G/T]CAGAAACACAAGACA | 51455 |
| rs375682750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99459005 | CGAGGTCAGGAGATC[A/G]AGACCATACTGGCTA | 51455 |
| rs375724757 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422497 | ACTGTAGGTAGGTTA[C/T]AATCAGATTAAGATC | 51455 |
| rs375754743 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415539 | AACTGAACTTTCTGC[A/G]GTGATGGAAATGTTC | 51455 |
| rs375775490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99473758 | ACAGAATTCAAAGAA[C/T]TTCAATCTATCAAAG | 51455 |
| rs375778776 | snp | C/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402954 | ACTTCTGGGGACTGC[C/G]ACAGGCCCCTGGCAG | 51455 |
| rs375801011 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99435529 | CACCATAAAATTTCC[A/C]TTCATTAACAAGGAA | 51455 |
| rs375844379 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99402831 | AGGATAAAATTGCTA[C/T]ATTCACACATTATCC | 51455 |
| rs375867490 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99441754 | AAAAACTTATTAACA[A/C]TTAAGATCCACTAGT | 51455 |
| rs375878960 | snp | A/T | 4.1289e-05 | 0.00454344 | intron-variant | REV1 | GRCh38.p7 | 2:99429796 | ATATAAAAATAATTA[A/T]CCAAATTATTCATTA | 51455 |
| rs375925680 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491776 | TTTCTTTTCCACTCT[C/T]GTATTCAAACCGAAG | 51455 |
| rs376001761 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490134 | CGCGCTCTGCTCCCC[C/G]CGGCCCGGGGCGACC | 51455 |
| rs376027059 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409515 | ACGAATCTTACATGA[A/G]GTTTAATATTAAGTA | 51455 |
| rs376033112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99451916 | CTGGCATGCTAACTG[C/T]TGGCATGCATGGTCG | 51455 |
| rs376104384 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463786 | TCACCACTATGCCCA[G/T]CTAATTTTTGTATTT | 51455 |
| rs376111217 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99485949 | GGGCAAAACAGTAGG[A/C]CCCCATCTTTACAAA | 51455 |
| rs376178795 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99403667 | CTCTTTGTCTTCATT[C/T]TTGTTACATGCCACT | 51455 |
| rs376222421 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439141 | GAGTGTGTCCATTAA[A/G]AATGGCAGTGCTCCC | 51455 |
| rs376228281 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430541 | CATGTCACATTATCC[C/T]CCGCTACAGGTAATT | 51455 |
| rs376239630 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99426024 | CTGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 51455 |
| rs376240595 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429039 | TCTAAGACTCTGTTT[A/C/T]GATTTGAAATTATTG | 51455 |
| rs376244607 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453576 | AATGTCCTTGATGTA[C/T]TAGCAAAGAATAAAC | 51455 |
| rs376253392 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490352 | TCCTGCTCCGGTCAC[C/T]CCCGCGCTTCGTTGA | 51455 |
| rs376393420 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99435671 | GAGAAAGAAAAACTC[-/T]TAATTTCCCTATACC | 51455 |
| rs376414211 | snp | C/G | 4.95618e-05 | 0.00497779 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434359 | TCAGGATTTTATTCT[C/G]GTAATACTGCCACTC | 51455 |
| rs376416235 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99451137 | CAGTGAGAAGTATCA[A/C]ATTAAAGGCTACATT | 51455 |
| rs376416750 | snp | C/T | 3.31455e-05 | 0.00407083 | intron-variant | REV1 | GRCh38.p7 | 2:99401380 | AGAGAAGAAATGTCA[C/T]TAGGAATTAGGAAAG | 51455 |
| rs376484891 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411756 | GTCGAAAATTCTTTT[C/G]TAACTATGTTAATAA | 51455 |
| rs376513968 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400079 | CAGTAAGCAAGCTCT[A/G]TTAGGCTTCCATGTT | 51455 |
| rs376561527 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99443524 | GAATACAGGAAAACA[C/T]ACTAACAGATTCTAA | 51455 |
| rs376595456 | snp | C/T | 6.85659e-05 | 0.00585476 | intron-variant | REV1 | GRCh38.p7 | 2:99434293 | AATCCAGAAGCCATC[C/T]ACAGGAGCACTAAGA | 51455 |
| rs376640904 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99404327 | TCCCCTCCCCTCCCC[C/T]CCCCAGTGGATGTGG | 51455 |
| rs376663157 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482429 | TGTAGTGGGAACTCC[A/G]AAAGTTGTAGCCAGT | 51455 |
| rs376695603 | in-del | -/GTTT | | | intron-variant | REV1 | GRCh38.p7 | 2:99452596 | TTACCATGTCTGTTT[-/GTTT]ACTTGTTTACTGTCA | 51455 |
| rs376753091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425848 | TCGAGACCACCCTGA[C/T]CAGCATGGAGAAACC | 51455 |
| rs376768586 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99465973 | TTGAGACGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 51455 |
| rs376775147 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99489405 | AATGGCGCGGAACTG[A/C]ATGGCCGGCCGAGGC | 51455 |
| rs376853594 | in-del | -/AT | | | intron-variant | REV1 | GRCh38.p7 | 2:99430527 | TTTTCTTTTGTACAC[-/AT]GTCACATTATCCCCC | 51455 |
| rs376905681 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418543 | TGAAAGTCAATTTCA[A/T]CATCCTCCCTTTTAA | 51455 |
| rs376926758 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99471608 | ACAGGGCAAAAAAGG[C/G]TTAAAAGGCAATCCA | 51455 |
| rs376940286 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | REV1 | GRCh38.p7 | 2:99460756 | GTTATAATGAAATCT[G/T]AATAACAAGAGCAAA | 51455 |
| rs376998648 | in-del | -/CATTCT | | | intron-variant | REV1 | GRCh38.p7 | 2:99430871 | TAAAAAAAAAAATCA[-/CATTCT]AAAACCACAACCTCA | 51455 |
| rs377032695 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99479345 | AAAAAAAAAAAAAAA[-/C]AAAAAGATTACAGGC | 51455 |
| rs377045705 | snp | G/T | 1.92799e-05 | 0.00310477 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439319 | GTGATTTCTAAAGCA[G/T]GAAAAAATTTTTGAG | 51455 |
| rs377083132 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99446160 | CCACATGGGCCATCT[A/G]TAACAAGCTTAATTA | 51455 |
| rs377140119 | snp | C/G/T | 3.35814e-05 | 0.00409753 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401201 | CCTCACAAGCACTTA[C/G/T]GGCACAGCTATCAGA | 51455 |
| rs377145300 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99447824 | CTCCTGGGTTCACGC[A/G]ATTCTCCTGCCTCAG | 51455 |
| rs377206186 | snp | G/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424228 | CAGCTTGAAGATTAG[G/T]ACATAGTTGTTTAGC | 51455 |
| rs377331291 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99441202 | TTAAAAGCTACAGGT[A/C]ACATGAAAAATATTT | 51455 |
| rs377362740 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99458947 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51455 |
| rs377372759 | snp | C/T | 3.29723e-05 | 0.00406018 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418918 | GTTTTGCTTTTCTAG[C/T]TGCCATTCTAGCCAG | 51455 |
| rs377381654 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99410172 | AATGCCACCATGTCC[A/G]GCTAATTTTTGTACT | 51455 |
| rs377402840 | snp | A/G | 9.00455e-05 | 0.00670929 | intron-variant | REV1 | GRCh38.p7 | 2:99403127 | AGCAGATGGATATAA[A/G]ATCCTCAACAAAATG | 51455 |
| rs377407385 | snp | C/G | 9.96641e-05 | 0.00705848 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406476 | TGGAACCAACTGATT[C/G]ACGTGAATCCCAACC | 51455 |
| rs377407501 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443805 | CGAAACCCTAAAATT[C/T]GACTATTTTTTACTT | 51455 |
| rs377417310 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484787 | AAATTTAACGGCAAG[C/G]TTCCAAACAAAAACC | 51455 |
| rs377417372 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430383 | CTTTGCTGTTTCCTA[A/G]AAGAACTATCTGTAA | 51455 |
| rs377417613 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99453032 | AATTAAGAGCTAAAA[A/C]TTATAAATTACTGAG | 51455 |
| rs377450555 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453923 | AAAAAAAAATCAAAA[A/T]AAAACAAAACTAGAT | 51455 |
| rs377461337 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99443921 | GATCTCGGCTTCACG[A/C]CATTCTCCTGCCTCA | 51455 |
| rs377462259 | snp | A/G | | | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479977 | GAAGGTAGGTGGGAA[A/G]GGGTGACATGAAGGC | 51455 |
| rs377468862 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99485252 | TCAAGTTGTATTAGC[C/T]GAAAATATCTATTAT | 51455 |
| rs377537606 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404459 | CTGTGAAAATGCTGG[A/C]AGGGCTATTAAATTT | 51455 |
| rs377543918 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | REV1 | GRCh38.p7 | 2:99442502 | ACCAATTTAGAGTTC[C/T]ATACTTGGTGACAAT | 51455 |
| rs377550196 | snp | C/T | 0.000264074 | 0.0114877 | intron-variant | REV1 | GRCh38.p7 | 2:99404407 | AGGGGGGTGAGAATA[C/T]TGAAACTACAGCAGA | 51455 |
| rs377556759 | snp | A/G | 2.0269e-05 | 0.00318341 | intron-variant | REV1 | GRCh38.p7 | 2:99429800 | AAAAATAATTAACCA[A/G]ATTATTCATTAAGAA | 51455 |
| rs377595784 | snp | C/G/T | 5.2673e-05 | 0.00513169 | intron-variant | REV1 | GRCh38.p7 | 2:99407985 | CTCAAAAATGAGAGA[C/G/T]ACATTACACAAAGTC | 51455 |
| rs377655343 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411321 | CAACAAAAACTGTTT[C/G]GTATACCCTCAACTA | 51455 |
| rs377658315 | in-del | -/ACCAGTAAGCAAGCTCTGT | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400062 | AGAAAACAGACATCC[-/ACCAGTAAGCAAGCTCTGT]TAGGCTTCCATGTTA | 51455 |
| rs377674533 | in-del | -/GATTCCTGGAAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99487251 | AGCTGCCAAATCATG[-/GATTCCTGGAAT]CTATGCCCTGATGGC | 51455 |
| rs377714591 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99401775 | CCTAGAACACTCAAA[-/AA]TTTTTTTTTATTTTG | 51455 |
| rs377748825 | snp | A/G | 0.00014084 | 0.00839048 | intron-variant | REV1 | GRCh38.p7 | 2:99403822 | AGGGTCCACCTAGTG[A/G]AAAAGACGAGGTCAA | 51455 |
| rs377766515 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99478533 | TTCACTAAGGAGAAG[G/T]GGTATAATCTCACAG | 51455 |
| rs386574732 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99471432 | AAAAAAAAACTTAAA[-/A]GTGTACAAAAGACAT | 51455 |
| rs386648490 | in-del | ACA/CCCCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99409863 | AAACAACCCCCCCCC[ACA/CCCCC]AAAAAAAACAGCGTT | 51455 |
| rs386648491 | in-del | A/CCCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99409864 | AACAACCCCCCCCCC[A/CCCC]AAAAAAAACAGCGTT | 51455 |
| rs386648492 | multinucleotide-polymorphism | CTAAAGAACCTGGCTGATCTTATAG/TTAAAGAACCTGGCTGATCTTATAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99451092 | TTTCTTTCTCTAACA[lengthTooLong]AATAACAGTGAGAAG | 51455 |
| rs386648493 | multinucleotide-polymorphism | ATA/GTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99459011 | CAGGAGATCAAGACC[ATA/GTC]CTGGCTAACACGGTG | 51455 |
| rs386648494 | in-del | A/TCTTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99485296 | TCTCCATCAATTCTT[A/TCTTC]TCTTATTTCTGTATC | 51455 |
| rs397746037 | in-del | -/G | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99405216 | TCCACTGTTCCTTTG[-/G]CCAGGGCCTACCTGT | 51455 |
| rs397839515 | in-del | -/C | 0.496907 | 0.039204 | intron-variant | REV1 | GRCh38.p7 | 2:99403151 | TGTCATCCAGACTAT[-/C]CATACTATCATTTTG | 51455 |
| rs397844261 | in-del | -/C | 0.354484 | 0.227119 | intron-variant | REV1 | GRCh38.p7 | 2:99449761 | TTCATTACTTGAGGT[-/C]CCTATTTGCTCTGCT | 51455 |
| rs397844262 | in-del | -/A | 0.490547 | 0.068097 | intron-variant | REV1 | GRCh38.p7 | 2:99449682 | GAAGGGGGATGTACT[-/A]AAAGCAACATAGCTT | 51455 |
| rs397844263 | in-del | -/CAT | 0.0314056 | 0.121312 | intron-variant | REV1 | GRCh38.p7 | 2:99403534 | AGTATGAGTAAATAT[-/CAT]CATATTTCTAGTTGG | 51455 |
| rs397844264 | in-del | -/GTC | 0.0105817 | 0.0719645 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402600 | CAAGGCTGAGATGTA[-/GTC]GTCTCATGATTTGAG | 51455 |
| rs397844265 | in-del | -/G | 0.485817 | 0.0830076 | intron-variant | REV1 | GRCh38.p7 | 2:99401902 | AAAAATAAATAATCT[-/G]GGGGGGGTGGTGGTG | 51455 |
| rs397985287 | in-del | -/G | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99477085 | TGCCATCGTGGAGTT[-/G]GGGGTCCCAAGACCA | 51455 |
| rs398060386 | in-del | -/AAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99476578 | AATAATAATAATAAT[-/AAT]GTCCACCCTGTTAAG | 51455 |
| rs398080454 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99449681 | AAAGCTATGTTGCTT[-/T]TAGTACATCCCCCTT | 51455 |
| rs527265141 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | REV1 | GRCh38.p7 | 2:99486520 | GGCGACAGAGCGAGA[C/T]TCCATCTCAAAAAAA | 51455 |
| rs527265203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99478804 | ATTCAGTGAGTCTAG[A/G]GCAGGGCTGGAAATT | 51455 |
| rs527273580 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99434245 | TGCTACAACTCTGCA[C/T]TCATTTCTATTAACA | 51455 |
| rs527298909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485990 | ACTAGCCAGGCATGG[C/T]GGCACATGCCTGTAG | 51455 |
| rs527339687 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99453993 | CACTGTTTTGAAATG[G/T]CAGAGTGAGTGCTTT | 51455 |
| rs527366014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99441228 | TATTTGAATATGCTT[A/G]TGAGTACAAGTTAAA | 51455 |
| rs527404017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448795 | AACACGCTTGCTCCA[C/T]CTTCTCCCATAACTG | 51455 |
| rs527500973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99409945 | TTTTTACCAATTAAA[G/T]GTATACACCTATGTA | 51455 |
| rs527503674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99402047 | CTTCCTATGGTTTTT[A/T]AATCACATGTAAGAC | 51455 |
| rs527564285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455714 | ATTTCCAAAAAATTA[C/G]ACTTGTCAACACTAA | 51455 |
| rs527568156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463979 | ACAGAGGGCTTAAAA[C/T]GAATTATTTCAGGTA | 51455 |
| rs527606568 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99464553 | TTCCAGGTTGAGATA[C/T]ATAAAGCTGAATAAT | 51455 |
| rs527643981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404875 | TCATTGAAGCCTGAA[A/G]TACTATGTGTAGTCT | 51455 |
| rs527696718 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425627 | AAACTTTATCAGAAA[A/G]CAGAAAAAAGGTCTG | 51455 |
| rs527706510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404339 | CCCTCCCCAGTGGAT[A/G]TGGTGTCAGATACAG | 51455 |
| rs527731591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458954 | TGGCTCACACCTGTA[A/G]TCCCAGCACTTTGGG | 51455 |
| rs527752389 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99486885 | AACAGGGCTGGCAGC[A/C]AACAAGTCTAAGGGG | 51455 |
| rs527809671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99403889 | TCTCTTTTTCACAAA[A/C]CAGACTTTGTTTTCA | 51455 |
| rs527810732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465851 | AAATCAGCTCTGATA[C/T]GATCTATGAGAATTT | 51455 |
| rs527811493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457600 | TGAGGTACAAGAATC[A/G]CTTGAGCCAGGGAGG | 51455 |
| rs527838851 | snp | A/G | 1.65905e-05 | 0.0028801 | intron-variant | REV1 | GRCh38.p7 | 2:99465025 | TGTCAATTTTATAAC[A/G]TAATGTATTTCTAAA | 51455 |
| rs527847969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472535 | ATGTATCGTACCACA[A/G]TTAAGAAGAAAAGAG | 51455 |
| rs527872723 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410786 | TTTTGAGAGTTAGAC[A/G]TTTACCCTTCATGCC | 51455 |
| rs527885043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418331 | TGAGTGGAGTTAATT[G/T]AAAACACAATCCTTC | 51455 |
| rs527957223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426709 | AAGTGTCTCAAAGTG[C/T]CTCTTCATTACCGTG | 51455 |
| rs527998086 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411822 | TTACAGCCCAAACAT[C/G]ATCTATCTCCATGCC | 51455 |
| rs528011486 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | REV1 | GRCh38.p7 | 2:99479299 | GCTACTGCACTCCAG[C/G]CTGGGTGACAGAGCG | 51455 |
| rs528080287 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99412568 | TTATCTGGGGCTACA[C/G/T]CTTACCACACAGTGC | 51455 |
| rs528097590 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99404852 | TTTTGGAACGTCTTG[A/G]CCTTTTGTCATTGAA | 51455 |
| rs528141064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99420092 | TAAAAACAAAAAAAT[A/G]AAATTGTGCCTGACA | 51455 |
| rs528169896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466613 | TGTTTGTTGACATTT[A/G]TAACAATTTGAATTT | 51455 |
| rs528177765 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466522 | GCTAGGATTACAGGC[A/G]TGAGCCACCATGCCT | 51455 |
| rs528191070 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99474174 | CATTACTAGTAATAC[C/G]TTTCACTTCTGAAGT | 51455 |
| rs528268700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99436991 | CCAACTTTTTTTTTG[C/T]TTTTTTTTTTTTTTT | 51455 |
| rs528346424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435184 | CAAAAATAAAGTCCT[A/G]GTTTTAACACAGCAG | 51455 |
| rs528401661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451213 | CTAAAAAATTAATTT[A/G]CAAGTTAATCTGTAA | 51455 |
| rs528419164 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99488240 | GCTCTTATGTAGAAT[A/C]AGAGTTTTGAAGTTG | 51455 |
| rs528437800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483821 | GGGAAAACCTAGGGT[C/T]TCATCTTATTTCTCC | 51455 |
| rs528473417 | snp | A/C | 0.000166105 | 0.00911179 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429910 | CATTTGCTTGCGCAG[A/C]ATCTGGATTCTCCCA | 51455 |
| rs528500303 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99470590 | CAAGCGTTAGGTCAT[-/A]AGCCTGTTCCTCTTC | 51455 |
| rs528534652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99446437 | TATGATCTCCCTAGG[C/T]GCATCTGGCAAAAAG | 51455 |
| rs528626449 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416110 | ATTTATGGGTACAAG[A/G]GACTAAAGAGGTTGG | 51455 |
| rs528664310 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99401443 | AAAATTGACTTTGGC[-/A]AAAAAAAAAAAAAAG | 51455 |
| rs528680788 | in-del | -/CCTAC | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99488766 | AAGGTTATGGTTGGT[-/CCTAC]CCTACCTAAACAGGA | 51455 |
| rs528696206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99406551 | AAATATGAATTCAGC[C/T]AAGCAAAATCCTCAG | 51455 |
| rs528709418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453532 | AATCCTTCTCTTGTT[A/G]CCCACCCTTCAGTAT | 51455 |
| rs528720774 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99467262 | ACAAAAACAAAAATT[-/A]AAAAAAAAAAACAGC | 51455 |
| rs528742772 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99442797 | AATAAACTGAATAAG[G/T]ATGCTCAATTTCCAA | 51455 |
| rs528746137 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99452533 | CAGAACCCATCTCTG[C/G]AATGTACTGTAACAG | 51455 |
| rs528811652 | snp | G/T | 3.29603e-05 | 0.00405944 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406001 | TTCCCTGAAGACTCA[G/T]CCTTGTTAGTATCAG | 51455 |
| rs528812956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99413563 | TTTTAATCAAAAGGA[C/T]GATCTCTCTGAAGAG | 51455 |
| rs528832360 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99473420 | AAAAATTCAGACACC[A/T]AGGTGAAGGGCACAA | 51455 |
| rs528868378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428158 | CTTAGCAAGGGTAAA[C/T]GGAGCTCGCATTTTA | 51455 |
| rs528879735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420003 | AAATATAAAGTGGGA[C/T]TTTGGCATTACATAT | 51455 |
| rs528927666 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99427548 | GAAAACTCACCAGTG[C/T]ATCAAACTGAGCAGA | 51455 |
| rs528928240 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99475265 | TTCTGTATTTGTTCC[A/G]ATTGGCTAGCAACTT | 51455 |
| rs528977647 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99472774 | TTTATGAGTGACTAA[C/G]TACATAAAGTGCTAG | 51455 |
| rs529114126 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99443307 | CCTAAAATATATACC[A/G]AGGAATCATCCCTCA | 51455 |
| rs529118487 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442388 | TCTGCATACAGGATT[A/G]AAGCTGAGACCTTTC | 51455 |
| rs529147572 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99452542 | CTCTGCAATGTACTG[-/T]TAACAGTTAACTTTC | 51455 |
| rs529156079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450711 | TAAAAAGGTGAAATT[A/T]ATTTTATTTAACCCA | 51455 |
| rs529180640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99449641 | TTGCCAGTAAACAAA[A/G]CTGGGAGGTAAATCA | 51455 |
| rs529197904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99404227 | TAGCATGCCCTCCCC[C/T]GTCTCTTCCCTGCTG | 51455 |
| rs529201266 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99488746 | AGAACTCCATAGAAA[A/G]AACCAAGGTTATGGT | 51455 |
| rs529213609 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490182 | ACCGCGGCGCCCGGC[A/G]TCGGCCTCCGTGTTC | 51455 |
| rs529252379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489280 | CCGGGGACGTCGAAG[A/G]CGGGGTGCGGAAAAA | 51455 |
| rs529288038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428849 | ACAAAAAAATTAGCC[A/G]GGTGTGGTGGCGAGC | 51455 |
| rs529296408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437558 | TTTTTCAAAATATCA[C/T]ATAAACATAATGCAA | 51455 |
| rs529298944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445283 | ATGTAAGCACATGAC[A/G]AACGTATATGGTTTG | 51455 |
| rs529392997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99452391 | TTGCACCACTGCACT[C/T]CAGCCTGGTTGACAG | 51455 |
| rs529485774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99459204 | CAGAGTGAGACTCTG[C/T]CTCAAAAAAAAAAAA | 51455 |
| rs529504787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451597 | GTGACTTTGGAGAAG[C/T]TGTTTAACTTCTTTA | 51455 |
| rs529509115 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99420275 | AAATCCTGCTGGCTG[G/T]GGAGAGACTGCCCTC | 51455 |
| rs529521023 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99467263 | ACAAAAACAAAAATT[A/T]AAAAAAAAAACAGCT | 51455 |
| rs529542579 | snp | G/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491698 | GAGTTTTGTTTTGGT[G/T]GTTGTTCTTTTGCTT | 51455 |
| rs529557169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466478 | AACCTCTGACCTCAG[A/G]TGATCTGCCCGCCTA | 51455 |
| rs529762233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454277 | AGAAAAGGCTGGGCA[C/T]GGTGGGTCACACCTG | 51455 |
| rs529771322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407050 | CCCTTTACTTACATA[G/T]GCACACATAAAACTA | 51455 |
| rs529774259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414196 | TGCTAACTTCTGTTC[A/G]TAGCTCCCATCCTCC | 51455 |
| rs529811926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475809 | TCAACATGGTAAAAC[C/T]CCATCTCTACTAAAA | 51455 |
| rs529838400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99460171 | AACCTCCGCCTCCCG[A/G]GTTCAAGTGATTCTC | 51455 |
| rs529857739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468465 | CTGAATTACAATGTG[A/T]CCTCTTGACTAAACC | 51455 |
| rs529907930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421842 | GTGTGTTCTCTTTCT[C/T]CTTATTAACTACCAA | 51455 |
| rs529973364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482770 | ATTAAAAAATTTACA[C/T]TTTGGGAGGCCGAGG | 51455 |
| rs530001069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475014 | TTTAGTTCCTCCGTA[C/T]GTGGAAAGAGTTGGA | 51455 |
| rs530044218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99424977 | TGGAGCATTCACCAC[A/G]AAACTATAATTATGG | 51455 |
| rs530047249 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99417578 | CATGCATATGGGGAA[A/G]GCCATGTGAAGACAC | 51455 |
| rs530082991 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99421012 | AGCTGTGGAAACAAA[C/G]TACAAGGTTTAAAGA | 51455 |
| rs530091288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431714 | AGAGGCAGCACCATC[A/G]TGTTCCTCTCCATTG | 51455 |
| rs530104530 | snp | G/T | 0.00156731 | 0.0279499 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424259 | ATGCCCAAAAAACAT[G/T]CCGTTCTTAATGCCA | 51455 |
| rs530133930 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99477586 | ATCTGAGCATTTTAA[C/T]ATGATTTTGATTCAA | 51455 |
| rs530141031 | in-del | -/AATAATAATAAT | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99476554 | GAGCAAGAATCTGTC[-/AATAATAATAAT]AATAATAATAATAAT | 51455 |
| rs530209534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469918 | CGAGGTCAGGAGATC[A/G]AGACCATACTGGCTA | 51455 |
| rs530260808 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439764 | TACTACATGGTCAAT[A/G]AATATCTGCTGAATT | 51455 |
| rs530421063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99454766 | AAATAAAATTCCACA[A/G]TACTCCTACTATTAG | 51455 |
| rs530487255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412662 | GGGTCTAATGGTTTA[A/G]TTGTAGAGGTAGGAC | 51455 |
| rs530571221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99460146 | CAGTGGCGCAATCTC[A/G]GCTCACTTCAACCTC | 51455 |
| rs530573672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482482 | CAAGTCCTGGAGTTT[A/G]TAGCTAATATAAGAA | 51455 |
| rs530601858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468342 | CTTCTTTAAATAGGA[C/T]TTTCCCTAGAACGGA | 51455 |
| rs530614058 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462263 | AATTTCCCGTTTTTC[A/G]TTTTAAACCTCACGT | 51455 |
| rs530617808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429241 | AAGATATATATATAT[A/G]AGTGTGTGTGTGTTT | 51455 |
| rs530675593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474259 | CATAGAGTGAGTCAG[A/C]CAAGTCCTATTTATT | 51455 |
| rs530712598 | snp | G/T | 6.58924e-05 | 0.0057395 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404488 | TTATTCCTGCGTCAC[G/T]GTTCGATTCTTGAGG | 51455 |
| rs530731771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99420871 | TGGCAAGAAAAGGGG[C/T]ATCTTGCCAGAAGGT | 51455 |
| rs530747833 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437091 | CTCAAACAATCCTCC[C/T]GCCTCAGCCTCCCAA | 51455 |
| rs530765719 | snp | A/G | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99476635 | GAGCCACTCCAGATA[A/G]TTTTGCACTGTGATT | 51455 |
| rs530809809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424115 | TAGCTAAAAGAAGGA[A/G]AACACAGACACAAAA | 51455 |
| rs530898716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484294 | GCTTAATACCTGAGT[A/G]ATGAAACAATCTGTA | 51455 |
| rs530976428 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99447218 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCATT | 51455 |
| rs531013014 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444066 | ACCTCGTGATCCACC[C/T]GCCTCTGCCTCCCAA | 51455 |
| rs531060538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483993 | TACAAATTAAAAAAG[A/C]CTTGCAAGGAAATGT | 51455 |
| rs531073856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445462 | CACGCTACAAGGTTC[C/T]CAATCTACAAGGATC | 51455 |
| rs531075570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99454137 | GTTCATGCTTGTAAT[C/T]TGAAAGATTTGGGAG | 51455 |
| rs531085670 | in-del | -/AACTT | | | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400368 | TTGTTGCAGACACAA[-/AACTT]AACTTAATGATTCAT | 51455 |
| rs531102878 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99470022 | GCTACGTGGGAGGCT[A/G]AGGCAGGAGAATGGC | 51455 |
| rs531115892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461147 | AACTTCCCAATGCTG[C/T]ACCAGCATTTATTTT | 51455 |
| rs531185879 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99470046 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 51455 |
| rs531219645 | in-del | -/AAGAAAAGAAAGCTA | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99441102 | TTTATTAATGTGGGT[-/AAGAAAAGAAAGCTA]AAGCTACGTATTCTG | 51455 |
| rs531299119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99485099 | GGGTTTAGGATCCTA[C/T]TACTTGTTAAAGTTC | 51455 |
| rs531323091 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432082 | GGGTAAAAGGCCCCA[A/G]CCATGAAATTTGGAG | 51455 |
| rs531353029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401969 | GCCAGGCTGGTCTCA[A/T]ACGATCCACCCACCC | 51455 |
| rs531364170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99448722 | TTTGTTCATTGTTAT[C/T]TCCCAAGAACACAGA | 51455 |
| rs531407849 | in-del | -/ATC | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99454091 | GACTGCAATGGCTCT[-/ATC]ATCATAGCTCACTGT | 51455 |
| rs531440414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99462772 | TCATAAACATAAACC[A/G]TAAGGCAAGGCAATA | 51455 |
| rs531458958 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99484952 | TATACGGTAGCTGTA[C/G]ATATTAATTAAGACA | 51455 |
| rs531478365 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99434616 | TATCAATCACCATGT[-/A]AATGTCATTTAAGTT | 51455 |
| rs531480123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470404 | TCAGACTCTCCTCCC[C/T]GTGTAATTAGGAATA | 51455 |
| rs531509864 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99476354 | CAAGGTTAGGAGTTC[A/G]AGACCAGCCTGGCCA | 51455 |
| rs531513790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469817 | TTTACTATCTACCCC[A/G]AGAATTATGTTTATC | 51455 |
| rs531560384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408366 | TTTAAGGTAAAAACC[A/G]TAATGGACACTTAGG | 51455 |
| rs531560513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416291 | TTCTTTTCTAAAATA[A/T]TTCCCAGGACTTTCA | 51455 |
| rs531578312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99454994 | TGAAGACCACTTTCA[C/T]GTCTGTAGGCCCAGC | 51455 |
| rs531603075 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | REV1 | GRCh38.p7 | 2:99456327 | TCTGTGCCCCGTGAT[A/G]GCACTTGTATTCCAC | 51455 |
| rs531722604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459164 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 51455 |
| rs531728672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99410079 | GCACTGGCGCGATCT[C/T]AGCTCACTGCAACCT | 51455 |
| rs531808974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99417440 | TGAGTCACCATGCCC[A/G]GCCACAGTGTGACTG | 51455 |
| rs531823176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99425997 | GCCGAGATCGCGCCA[C/T]TACACTCCAGCCTGG | 51455 |
| rs531855889 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460550 | TTTTTAAATCAAAAA[C/T]AAAATAGCACCTCCT | 51455 |
| rs531865860 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99425915 | GTGGCGCATGCCTGT[A/C]ATCCCAGCTACTTGG | 51455 |
| rs531867683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418213 | AGACTTTACAAAGCT[A/G]ACAGAGGCACTTTAT | 51455 |
| rs531885342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99479201 | GGTGTGGTGGCACTC[A/C]CCTGTAGTCCCAGCT | 51455 |
| rs531908399 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99485907 | GATGAGGCAGGAGAC[G/T]GTAGCCCAAGAGTTT | 51455 |
| rs531995810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433005 | CCTACCAGAGAGACT[A/C]TGAGCACTGAAGATG | 51455 |
| rs532087189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401849 | CAATCATGGTTCACC[A/G]CAGCCTCCACCTCCC | 51455 |
| rs532151519 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411493 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 51455 |
| rs532192037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447590 | TATATATTACACCTC[C/T]ACAACATGCTAGGCA | 51455 |
| rs532194122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455523 | TTGAGTACCAACTAG[G/T]TGCAAATTTCACATC | 51455 |
| rs532214598 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477993 | ATCCCAAGACTTTGG[A/G]AGGCCAAGGCAGGTG | 51455 |
| rs532230083 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99454879 | AGTAAAAGTAAAAGC[A/C]ATATACAAGGACCAC | 51455 |
| rs532267938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99476591 | ATAATGTCCACCCTG[C/T]TAAGTGCTTTTGTTT | 51455 |
| rs532326679 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407743 | TTCCTCACAGTCATA[A/G/T]CTACTTCTAGGAAAC | 51455 |
| rs532338234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415475 | AATACAGACATAGAG[A/G]AGTAAACTTCAAAGA | 51455 |
| rs532351205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423852 | CATCCTTCATCTATC[G/T]GGCTCCATGGGAAGA | 51455 |
| rs532373032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417385 | CTGGCCTCAAATGAT[C/G]CATCTGCCTCGGCCT | 51455 |
| rs532413946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423068 | TCTTTGTGTTAATAG[A/C]ATAGCTATAATAAGT | 51455 |
| rs532442956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99464056 | GAAAGAATACAATGA[A/G]TGCTCCAGTGGCTAA | 51455 |
| rs532545172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425136 | GTTATTCTATATATA[C/T]GTTCAATAAATATTT | 51455 |
| rs532609102 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99420532 | GAGCCTAGGCGCTCC[A/G]TCTGCCACTCCTTCA | 51455 |
| rs532610295 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99473703 | TTTTCTGCTGCAATA[A/G]AACAATTTCTGTACC | 51455 |
| rs532630770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471106 | ATGCAAAGAAAGCAG[A/C]CTGTGGCCACCCCTT | 51455 |
| rs532666854 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440483 | CAAGCTGGATGATCA[A/C]CCATTTCTGGGTTAG | 51455 |
| rs532670200 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | REV1 | GRCh38.p7 | 2:99470553 | CCTAAATATTTGCCC[C/G]GGCAAGCTTATACTG | 51455 |
| rs532683218 | in-del | -/AAAC | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99486925 | TAAGTGGGAAAAAAA[-/AAAC]AGTGTATCTTCACCT | 51455 |
| rs532694624 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99485770 | GTATTTTTTAAAGGC[A/G]TTCCATAAATACAAT | 51455 |
| rs532708869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477865 | GGGCTTCCTGAAACA[A/G]CGACTAATGCTTTTC | 51455 |
| rs532726266 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99414698 | AACATCAGGGAAGAC[-/TT]TGTGTCTCTCTTTTG | 51455 |
| rs532736069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432914 | TAGCTCTCTGCTACT[C/T]CTAAGGAATGTGAGC | 51455 |
| rs532835058 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417038 | ACAAAGAAAACTACA[A/T]AAAGGGTTCGATTTA | 51455 |
| rs532838588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443207 | TTTAAAAATAACCAA[C/T]CAATATACTTATGCT | 51455 |
| rs532853191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439875 | AGGTACTATTCAACA[C/T]ATTAAATCTAATACG | 51455 |
| rs532855163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99479384 | CTCGCCTGTCCTGCC[C/T]CCCACTTCCCCTTAC | 51455 |
| rs532874161 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450275 | ACACAATGTGACTTA[C/T]GCTTCCCCCTAAGAA | 51455 |
| rs532875320 | snp | A/C/T | 0.0219587 | 0.102456 | intron-variant | REV1 | GRCh38.p7 | 2:99442277 | AAAAAAAAAAAAAAA[A/C/T]CAACCAGCTTTGCAG | 51455 |
| rs532894647 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480201 | GGTGGTGCACGCCCA[G/T]GGCCACAGCTACTTG | 51455 |
| rs532914543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486795 | ACTGACAGCCTACTA[A/T]GTACCAGGCACAGTT | 51455 |
| rs532967813 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459638 | TTGAACCTGGGATGT[G/T]GAAGCTGCAGTGAGC | 51455 |
| rs532969196 | in-del | -/TTTT | | | intron-variant | REV1 | GRCh38.p7 | 2:99401776 | CCTAGAACACTCAAA[-/TTTT]TTTTTATTTTGTTTT | 51455 |
| rs533031756 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426390 | TCCCTATAAATATCA[C/T]GTTCTTATATTTACA | 51455 |
| rs533037721 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99428608 | ATAATTAGCAAATTT[-/A]AAAAAAAACTATTAT | 51455 |
| rs533074657 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433647 | CTTTCTGGGTAATAT[A/G]TTTCTGAGAAACTAA | 51455 |
| rs533146681 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99489007 | ATTATCTGCAATTTA[A/T]CTTACGGAGGAGTAC | 51455 |
| rs533170369 | snp | C/T | 4.94205e-05 | 0.0049707 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403701 | AAGGCTCACCAGATG[C/T]GCTGGCTGACTGCTG | 51455 |
| rs533198976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99452124 | AGCAGATGTGGGGTT[A/T]ATTAGAAAAAAAATT | 51455 |
| rs533279315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464778 | TTATAAACATCATAA[A/G]GCTTTCAATACACTG | 51455 |
| rs533293778 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430019 | TTTTTCAAGAAATTT[G/T]TTTTCCATTACTTTC | 51455 |
| rs533354039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444619 | GATATCCTCAGAGAT[A/G]CTCAATAAAAAGAAT | 51455 |
| rs533384455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467502 | CAGAGATCTGCCACC[A/C]CACCTCTCTTCCCCA | 51455 |
| rs533424722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473355 | CCTGGGCGACAGAGC[A/G]AGACTGTCTCAAAAA | 51455 |
| rs533533372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99416874 | GCCGAGATCGCACCA[C/T]TGCACTCTAGCCTGG | 51455 |
| rs533539690 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472070 | TATATCCAAAGGCAC[C/T]GAAACCTGAGACACA | 51455 |
| rs533568853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419959 | TAAAAGTAGTGAGTT[A/C]AGGGGAGGGGAAAGG | 51455 |
| rs533568868 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99411274 | GCCTGGGCGACAGAG[G/T]GAGACTCCGTCTCAA | 51455 |
| rs533630390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419368 | CAGGCGCCCACCACC[A/C]TGCCCGGCTAATTTT | 51455 |
| rs533684296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99477213 | AGACTACATTTCCCA[C/T]GCTCCTCTCAAAATC | 51455 |
| rs533719705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484649 | CTATTAAAACATTTC[A/C]CTTATAATACAAGCA | 51455 |
| rs533749770 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409139 | TTAAAGTAAATAAAT[A/G]AATGACCACTATTTA | 51455 |
| rs533762644 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461036 | CCTGTTTTCATTAAC[A/G]TTTTAATTTTTCATA | 51455 |
| rs533766858 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491943 | GAAAAAAAATCACGT[G/T]GCTGTCTACATAAAA | 51455 |
| rs533770917 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99451011 | AAACTGAACTACAGC[A/G]TCAGAGTGATTTAAT | 51455 |
| rs533812211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425294 | TTACTCAGCAGTAGA[C/T]GCAAAATCACATGCA | 51455 |
| rs533827168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424513 | ACTATGTCATTAAAA[C/T]ACCAGGTTTGGCTCT | 51455 |
| rs533843496 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432289 | TGCTATTTGTCCTAA[G/T]ACTTTGTCTAGACAT | 51455 |
| rs533884093 | in-del | -/TTAATCTTGATCTGTT | 0.0170251 | 0.090679 | downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400262 | AGAGATTTTTATACA[-/TTAATCTTGATCTGTT]TTAATCTTGATCTGT | 51455 |
| rs533896746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440704 | AAGAAGTCACAGATG[A/G]GCATTTCAAAGAAAT | 51455 |
| rs533956659 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99445164 | GAATGGCAAAAAAAA[-/T]CTCATGAGAGATAAA | 51455 |
| rs533972563 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463950 | TTTAGACTGGCTTCC[A/G]CTATCTCCCACATAC | 51455 |
| rs533985510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433684 | AAATTCTCTTTGGCT[C/T]TGCAAAACAACCATG | 51455 |
| rs534001120 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415329 | CAAATCTCAACGAAG[A/G]GAGAGTCAAGGAGGC | 51455 |
| rs534055682 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448583 | TCTAGGTCCACATTA[A/T]CTTGATGTATTACCA | 51455 |
| rs534130228 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402530 | GGGTAGCTGCTTTAA[A/G]CTTATCAGAGTTAGA | 51455 |
| rs534143872 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99474826 | ACAATCACTTGAACG[C/T]GGTAGGCAGAGGTTG | 51455 |
| rs534190496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486269 | GACCAGTGGCTCACG[A/C]CTGTAATCCCAGCAC | 51455 |
| rs534193530 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99409770 | ATTGCTTGAACCCAG[A/G]AGGTAGAAGTTGCAA | 51455 |
| rs534194362 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99444732 | ACTCCTAACTACCCC[C/T]GCTTGCCCATTTATC | 51455 |
| rs534246438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99442627 | TTAGTGGTCCTAATA[C/T]AATATGATCTTAGAG | 51455 |
| rs534279903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451022 | CAGCATCAGAGTGAT[C/T]TAATGTGAAACAGTA | 51455 |
| rs534317240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405311 | CCAGGAGTAACTAAT[C/T]GTGGGTATCTGTCGC | 51455 |
| rs534351597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457042 | GCTAAACATTTCGAT[C/T]CCTTTATGAAGTATT | 51455 |
| rs534387212 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482914 | CTCAACCACTTGGGA[C/G]GCTGAGGCAGGACAA | 51455 |
| rs534410762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458711 | TGAACAATAAAAAGG[A/C]AACAATTTTGATGAC | 51455 |
| rs534489936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419482 | CCCAAAGTGCTGGGA[C/T]TACAGGAATGAGCCA | 51455 |
| rs534497976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411085 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 51455 |
| rs534525513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472264 | TGCTACAACTTGCAT[A/G]AACCTTGAAGGCATT | 51455 |
| rs534540789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471265 | TAAGGAACTGGTTAA[C/T]AAAGGGCTTAAGGTA | 51455 |
| rs534548701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427587 | ACAATCTAGTCCCCA[C/T]TCCAAACTCAGTAAC | 51455 |
| rs534548766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418749 | CTGGGCAAAAAGAGG[G/T]CTCACAGTTCTATAT | 51455 |
| rs534616400 | snp | A/G | 6.58935e-05 | 0.00573955 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404588 | TTCTTTCTTTTTGTC[A/G]CCATGTGACTCTGCT | 51455 |
| rs534743698 | in-del | -/AGAG | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400246 | TTGATCTGTTTTAGT[-/AGAG]AGAGATTTTTATACA | 51455 |
| rs534749791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466096 | ACAGGTGCCCGCCAC[A/C]ACGCCCGATTATTAT | 51455 |
| rs534817195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437150 | ACGCCCAGCTAATTT[G/T]TTTTTTCTTTTTGGT | 51455 |
| rs534822003 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99473852 | AAGTATGATCTTTCC[A/C]TCTTTTCTTGGGACA | 51455 |
| rs534852955 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99465827 | GAAGCCTTATATATT[A/G]TCCACGTCAAATCAG | 51455 |
| rs534856715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481554 | GTTCTCACTTCTTTA[G/T]CCAGCATTGTGTAAT | 51455 |
| rs534928315 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99434546 | AAAAACATGCCTTTT[G/T]TTTCTTTAGCTTTAC | 51455 |
| rs534993495 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99413063 | TAAAATAATCTTTAA[A/T]GTCTTTAGGCAACAT | 51455 |
| rs534993965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99422007 | TGAAGAGTTGAAAAC[C/T]GGTGGGTGAATTTGA | 51455 |
| rs535043962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99466027 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 51455 |
| rs535072956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99420351 | GCACACTTGTCATAT[A/G]CAACCTAACCACCTC | 51455 |
| rs535094524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99455276 | TCACAATCTTATGAA[C/T]TAGAAAAGATAACTT | 51455 |
| rs535124600 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428282 | CCACCATTCATTAAC[G/T]TAGTAGAGAAAAAGA | 51455 |
| rs535157318 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482127 | AACTTGACCTCCAGG[C/G]AGAAGGGGACTGGGG | 51455 |
| rs535228914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489068 | TACAAACTGAGAATA[A/G]GTAGGAAGAGCAGCG | 51455 |
| rs535268885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471455 | AAAGACATAAATATA[A/G]GAGCTAAAACTATCA | 51455 |
| rs535310997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444256 | ATAAAATCCTAACCT[C/T]AGCTTTCCATCCTTT | 51455 |
| rs535332897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433633 | CTAACTTCTGACTAC[C/T]TTCTGGGTAATATAT | 51455 |
| rs535336138 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99426404 | ATGTTCTTATATTTA[A/C]AATATTTTCATTTTC | 51455 |
| rs535438166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404077 | GGCAAAATGCACTAG[C/T]AGAAAATGGGAAGCA | 51455 |
| rs535575740 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99477793 | CTTCTTGTTATTCAT[-/A]ACTACCAAAAAAAGA | 51455 |
| rs535593323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489034 | GTACATTAAGGAGTG[C/T]TATGTGAGATTATTT | 51455 |
| rs535620633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426977 | GTCACGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 51455 |
| rs535638136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488637 | AAGGCAGGGAACAAT[A/C]CGCAGCACTGGTCCC | 51455 |
| rs535766779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458504 | TAAAATACTACAACC[A/G]CTTTGGGTAACAGTT | 51455 |
| rs535796852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99486121 | CAGAGCAAGACCCTG[C/T]CTCAAAAAATGTTAA | 51455 |
| rs535824650 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99420281 | TGCTGGCTGGGGAGA[A/G]ACTGCCCTCCCAGGG | 51455 |
| rs535827045 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486862 | AAGACCTCTGCTCGC[C/T]TGTTGAGAACAGGGC | 51455 |
| rs535891052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437251 | GCCTCCGAAAGTGTG[C/T]GAATTACAGGCATGA | 51455 |
| rs535907190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427916 | CAAGGCATGAAGCTT[A/G]ACCAAATTTATAAAG | 51455 |
| rs535921002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99436390 | TCACAACTATGAGGT[A/G]GGTAATCGTATCATC | 51455 |
| rs535960282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435420 | CAAAACTATCCTACA[A/T]TCAAAAAGTTGGGAT | 51455 |
| rs535989354 | in-del | -/G | 0.278664 | 0.248351 | intron-variant | REV1 | GRCh38.p7 | 2:99489734 | GCTCTGGCCGCTGCC[-/G]GGGCGGGTCTGCGGC | 51455 |
| rs536034802 | snp | A/G | 8.54737e-05 | 0.00653679 | intron-variant | REV1 | GRCh38.p7 | 2:99406148 | CCTCTTCAGATCATC[A/G]GGCAGGGCCTTTAAT | 51455 |
| rs536062255 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462825 | GGGCGCAGTGGCTCA[C/T]ACCTGTAATCCCAGC | 51455 |
| rs536067341 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412887 | TGCCATGGTCATATA[C/G]TGCAAGTCTCCACAA | 51455 |
| rs536070327 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430921 | ATTATAAACAAAAGT[A/G]CCATGAGTAAAACAA | 51455 |
| rs536091157 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99443806 | GAAACCCTAAAATTC[G/T]ACTATTTTTTACTTT | 51455 |
| rs536107131 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460158 | CTCGGCTCACTTCAA[C/T]CTCCGCCTCCCGGGT | 51455 |
| rs536130421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450933 | AGAGATTTAAAAGCA[A/T]CCTTTTAAACAAAAT | 51455 |
| rs536207918 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99462209 | AAATGGACCTACAGT[A/G]AAGCTCACAGTTTAC | 51455 |
| rs536326758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445019 | TCTGATATATACATG[A/G]AAGAGTTTACATTCT | 51455 |
| rs536340576 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99461713 | ACTTTACAGTTCAGC[A/G]AAAGATAAAACTGAA | 51455 |
| rs536373406 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99412649 | TTTCAAGCATTGAGG[A/G]TCTAATGGTTTAGTT | 51455 |
| rs536464265 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99474478 | ACCTAACACAATTCA[A/C]CAAAACAGATGCTTC | 51455 |
| rs536490288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99422591 | TTTTAAGAACAGAAG[A/G]GTATATCTGGTATGA | 51455 |
| rs536503021 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99471429 | GTTAAAAAAAAACTT[-/A]AAAGTGTACAAAAGA | 51455 |
| rs536518250 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99412137 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATCTCTTG | 51455 |
| rs536540108 | in-del | -/CC | | | intron-variant | REV1 | GRCh38.p7 | 2:99409864 | AACAACCCCCCCCCC[-/CC]CCAAAAAAAACAGCG | 51455 |
| rs536549560 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99459086 | GGTGGTGGCCACCTG[C/T]AGTCCCAGCTACTCG | 51455 |
| rs536557703 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99404963 | TACTCACAGAATGTC[C/T]TGCAATTGGGGCCAA | 51455 |
| rs536639181 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401038 | TTGTAAATAGAATCT[A/G]TGCTACAGTAAAATA | 51455 |
| rs536652090 | snp | A/C | 6.7271e-05 | 0.00579922 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406079 | CTAGAAGCAGATGAT[A/C]TTTCCAGATCCACAG | 51455 |
| rs536743786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415187 | AGTTTTAACTAAATA[C/T]GTCAATTAAGTAGGT | 51455 |
| rs536769278 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448034 | ACCAGGTTATATGGA[C/T]ACTGAACTGCCGAGT | 51455 |
| rs536819863 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440450 | GTAATGAGAGCCTGA[A/C]TACACAGAAAAGTCC | 51455 |
| rs536858492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411744 | CATCACTGACTTGTC[A/G]AAAATTCTTTTGTAA | 51455 |
| rs536858742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420257 | AGTGTTTTGAAATCT[C/T]AAAAATCCTGCTGGC | 51455 |
| rs536908299 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99460533 | GTGAAATAAAGCTTA[-/T]TTTTTTAAATCAAAA | 51455 |
| rs536921034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428567 | TTTGAACTTAATGCT[C/T]TTTAACTTAAATATA | 51455 |
| rs536979641 | in-del | -/CTT | | | intron-variant | REV1 | GRCh38.p7 | 2:99416034 | ACTATTGTGTTTTTC[-/CTT]CTTATGTAGTTATTC | 51455 |
| rs536998760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99469264 | AGATTGTTCTTGAAG[A/G]AAAAGCACGACAACT | 51455 |
| rs537065043 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99465222 | TATATTTAAAATTCA[A/G]TAGAAAAATATCTTT | 51455 |
| rs537123159 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99422256 | AAAATCATCTCATAG[C/G/T]ATCTATCCACAAAAA | 51455 |
| rs537168679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459034 | TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 51455 |
| rs537171485 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459942 | AGGAATCAAGAACAC[C/T]TGGATTATTACAGTT | 51455 |
| rs537174470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475477 | TTTTGCTTCTAAGAG[A/T]AGTTACTATTTATTT | 51455 |
| rs537179061 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427072 | CAGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 51455 |
| rs537212568 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99474704 | ATCAGAAGTTTGAGA[C/T]CAGCCTGACCAACAT | 51455 |
| rs537237800 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99429508 | AAACAAAAGATTAGA[A/G]GGAATAAATATTAAA | 51455 |
| rs537275966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437696 | ACAGAACTAATTAAT[C/T]ATAGTTCTTAGAAGC | 51455 |
| rs537368958 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472901 | TATGTAACATTTAGA[A/C/T]ATAAAAATACAGCTG | 51455 |
| rs537378948 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438989 | CTGCAACTGCTGCAG[A/G]GTGCAGTCTCTGAAA | 51455 |
| rs537441853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414895 | GTTTAAAATTTTAGA[C/G]TATCTTGAGTATACC | 51455 |
| rs537454969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484511 | TCTTAAATCTAATGT[A/G]TTATATGCAAAACCT | 51455 |
| rs537491597 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413848 | AGGAAAAGACAGCGT[C/T]GTGTTTCTGGTCTTC | 51455 |
| rs537586515 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491869 | ACCTTGGCAATACCT[C/T]TATAGAATACAGTAA | 51455 |
| rs537636774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421221 | AATACGGTTTCCGTT[C/T]ACTTTTGGGAAAAAA | 51455 |
| rs537653591 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490405 | CCATTCGGACAGCGC[G/T]CCGCTCCGTGCACAG | 51455 |
| rs537665207 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99422709 | ACTGTGGATATTTTT[A/C]CCCTAAGAATAGAAA | 51455 |
| rs537679651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99428978 | GCCTGGGTGACAGAG[C/T]GAGACTCCGTCTCAA | 51455 |
| rs537681469 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99431318 | ATATGAATAACGTAT[A/G]CTAGCTATACTATTA | 51455 |
| rs537689283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447024 | ATTTTAATCAATACT[A/G]TATCATTGATAGACA | 51455 |
| rs537791144 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | REV1 | GRCh38.p7 | 2:99489446 | GAGGAAGGAGTTTGC[C/G]GCGCGGTCTGACCGG | 51455 |
| rs537906787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99430539 | CACATGTCACATTAT[A/C]CCCCGCTACAGGTAA | 51455 |
| rs537932701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448278 | CATACACTGATTATA[A/G]TCTATCCATACATAA | 51455 |
| rs537952005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447645 | GATTTTTATTTCTCA[C/T]ATAACCACAGCAGGC | 51455 |
| rs537985367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402441 | CTGCATTTCTACAAC[G/T]ATGTCACTAACAGCT | 51455 |
| rs537994814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484155 | CACATGTTCTCACTT[C/G]CAAGTGGCAGCCAAA | 51455 |
| rs538047929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99409644 | AAGTCAGGAGTTCAA[C/G]ATCAGCCTTGCCAAC | 51455 |
| rs538056064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408841 | AAGGAAAGTTATTTC[A/G]TGTTTTGGATGATCC | 51455 |
| rs538127303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415831 | GCAGAGGGCCCTTCA[C/T]TGAAGAGTGCATGCG | 51455 |
| rs538169853 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99451311 | ACGTCAAGAACACAT[A/T]AACTTTCCATATACA | 51455 |
| rs538176647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407791 | GTATATTAGCCCCTG[A/G]TTAATCAGGGGTACC | 51455 |
| rs538263915 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491229 | AATCCAACGAATTTA[A/G]ATTGCATACTTTTCA | 51455 |
| rs538393835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463391 | GGGTGTGGTGGTGCA[C/T]GCCTGTAATCCCAGT | 51455 |
| rs538443839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416806 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51455 |
| rs538459196 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458942 | GGCCGGGCGCGGTGG[C/T]TCACACCTGTAATCC | 51455 |
| rs538460669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407172 | TTGGCTCATGCAAGC[C/T]CTGCCTCTTGGGTTC | 51455 |
| rs538495098 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486452 | GAGAATGGCGTGAAC[C/G]CAGGAGGTGGAGCTT | 51455 |
| rs538497007 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452499 | ATATGACATTAAACA[C/T]TGTGTGACACACTGC | 51455 |
| rs538501271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99469317 | GTAATGAACTAAAAA[C/T]TAAGTACAAAATTTC | 51455 |
| rs538504291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425186 | TGCCTTGTTTTAAGA[A/C]ACGTATATACAAACA | 51455 |
| rs538528812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470602 | TCATAGCCTGTTCCT[C/T]TTCCTTATTTGAAGG | 51455 |
| rs538535417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462386 | TTATTTCTTCTCATC[G/T]TACAATCATTTGTCT | 51455 |
| rs538573630 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99470016 | GTCCCAGCTACGTGG[C/G]AGGCTGAGGCAGGAG | 51455 |
| rs538579694 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483426 | CAGTAAGCAACACTT[C/T]GCTTAATAGGCTATG | 51455 |
| rs538632478 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99443730 | GCTAAATGTTTTACC[A/G]AAATTCAGGTTACAT | 51455 |
| rs538657043 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99401677 | ACTGGAACCCAGGAG[C/G]CAGAGGCTGCAGTAA | 51455 |
| rs538714321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437843 | CACATAGGAATACAT[C/G]AAACTCAGTAAAACA | 51455 |
| rs538749880 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483565 | TCTCAAAGCATCCTA[G/T]GTGGATAAGGCAGTC | 51455 |
| rs538756909 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400706 | TATGTAGATTTCTCC[A/G]CATGGAAGAAGTAGT | 51455 |
| rs538773282 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490510 | AAACCCCGGTACTGT[C/G]TGAAGATGCGCCAGA | 51455 |
| rs538775852 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405586 | CTCTACTTCACCACT[A/G]ATCACCAAAGCTGCC | 51455 |
| rs538797895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453787 | AGTCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGA | 51455 |
| rs538803011 | snp | A/C/G | 0.000586532 | 0.0171154 | intron-variant | REV1 | GRCh38.p7 | 2:99442266 | TCAAAAAAAAAAAAA[A/C/G]AAAAAAAAAACCAAC | 51455 |
| rs538819494 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468337 | ATTTGCTTCTTTAAA[G/T]AGGACTTTCCCTAGA | 51455 |
| rs538822087 | in-del | -/TGATC | 0.00478085 | 0.0486577 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400216 | TTTATACATTAATCT[-/TGATC]TGATCTGTTTTAATC | 51455 |
| rs538858395 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99406123 | TACAAAAAGAAAATA[C/T]ATAAAATAGCCTCTT | 51455 |
| rs538884333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99424353 | TTATCAAATATGTTG[A/G]TATCTCCCCATGCCA | 51455 |
| rs538899603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413959 | TCTGAGTTTGAGGAC[A/G]ACATGGGCAACTGAG | 51455 |
| rs538940405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459746 | CAAAAAGGATAGAAG[G/T]CAAAGAAGTCAATCT | 51455 |
| rs538975569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99430322 | GACTGTACAGCTCTC[A/G]GTAGTGGGGAAAAGT | 51455 |
| rs539003121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471976 | GGGAATATAAAATGG[A/T]GCAGCTGATATGAGA | 51455 |
| rs539102001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463124 | AATATAAATACATAA[A/G]ACACATAGGTCAAAG | 51455 |
| rs539122967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458930 | TTGTAGTGTGGAGGC[C/T]GGGCGCGGTGGCTCA | 51455 |
| rs539176812 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478887 | GTACCTAAAAATGTA[A/C/T]CTATAGTGGTGATAA | 51455 |
| rs539212064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478428 | CATGTCCATAAGCAG[A/G]ATCAAGCTACGAAGG | 51455 |
| rs539259691 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99485351 | TTATGAAAAGAACAG[A/G]AAGATACAGAGCACA | 51455 |
| rs539275552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99441468 | TTAAAAGCTTAAATT[A/T]AAAAAAAAAAGCAGC | 51455 |
| rs539281169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432412 | ATATTTGGTGCCATG[A/T]CTGATAATGACCCAG | 51455 |
| rs539311622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440755 | ACCCCCCAAAAAAAC[C/T]CCAGAAAACAACAAA | 51455 |
| rs539332161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476897 | CGTAAGTGGACTCTT[C/T]TGTGTGCCCCATGCA | 51455 |
| rs539334397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469480 | AATTACAGGCTGTCA[A/G]TACAGCCATGTCCAG | 51455 |
| rs539348966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484403 | AAAAAAATTGCCCCA[G/T]AGTCAGCAGGAAACA | 51455 |
| rs539350225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448151 | ATACACTATACAAAG[G/T]AACTGAGTTAATACT | 51455 |
| rs539511740 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439643 | ATAGAACATTTCTCA[C/T]GGCTGAAGAAAAACC | 51455 |
| rs539513197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434722 | TCAGCCTTCCATGGT[C/T]TTTGTTTGATTTCGT | 51455 |
| rs539532091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433326 | TCTCAAAAATCTCTG[A/G]AAAGATTTAAAGACC | 51455 |
| rs539547567 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99462092 | CTTCTACAGACAAGA[C/G]AGTAAAAGATTCTTC | 51455 |
| rs539702840 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99435001 | TGTTAAGTTACAAGA[C/T]TACTATAAATTTGTA | 51455 |
| rs539709157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99403425 | AAGGACAACTAGCTG[A/T]ACAAGTATTTAAGAC | 51455 |
| rs539756636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99457185 | CAACTGCTATCTCTT[C/T]TCAAACATAGTTCCT | 51455 |
| rs539788412 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463550 | ATATCACAAAATATT[G/T]TTCTTATGTACACAA | 51455 |
| rs539822720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99488337 | CTACTTGAGACCTCA[C/T]AGAAATTAATTTTAA | 51455 |
| rs539823384 | snp | G/T | 1.65941e-05 | 0.00288041 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401228 | CAGAGAGCATCAGGC[G/T]CTCTGGTAATATTTA | 51455 |
| rs539890889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408267 | TAAAAGTGAATGCCA[G/T]AGTCTCCCTTCAAGG | 51455 |
| rs539942764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99442709 | TGACTTTAGTATTTA[C/T]CACCCTGTCAACAGT | 51455 |
| rs539942765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450839 | TTTACATTTACAACG[C/T]ATCTCAATTTAGAAT | 51455 |
| rs539959721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99466721 | ATAATACAAACGTTT[C/T]AGGGGCATGTGCAAG | 51455 |
| rs540000108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469723 | TTTTTCCTAATGTTT[C/T]ATCTTTTGCTGGAAC | 51455 |
| rs540021224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476488 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 51455 |
| rs540025745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99404004 | ATAAGGAATTAAGAG[C/T]AAGAATAAGGAATTA | 51455 |
| rs540062896 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99403404 | TCCTTTAATGTATTC[A/T]TCTCAAAGGACAACT | 51455 |
| rs540075956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450228 | CTTATATGTCTTAAA[C/T]ATTGGAAATATTTTA | 51455 |
| rs540142956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465184 | ATAAAACACCCTCCT[A/G]CACATGTTTAAATTG | 51455 |
| rs540197346 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99462692 | TTTTGAAAAAAAAAA[A/T]TTTTAAAAACTAAAT | 51455 |
| rs540206213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454843 | CTAAAACCAGACATA[A/G]TGACAGACAATTGAA | 51455 |
| rs540206517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408935 | TTATTATAAATTGAA[C/T]TGGATTTTCCCATAG | 51455 |
| rs540242116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461984 | GAATGAGAAAATGAA[G/T]AGAGAGACTAAGTGA | 51455 |
| rs540258357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425682 | TAATAATTATGCCAG[A/C]TATATAGATTCAGCA | 51455 |
| rs540351712 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99431721 | GCACCATCGTGTTCC[G/T]CTCCATTGGGCTGGC | 51455 |
| rs540388372 | in-del | -/A | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483018 | CAAAACTCCGTTTCA[-/A]AAAAAAAAAAAAAAA | 51455 |
| rs540433297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440417 | AGCCCCTCACCCTAA[C/T]ACCAACTTGGTTTAT | 51455 |
| rs540435233 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450181 | CAATTTTGTTTCAAA[C/T]GATTTATTCTTAATA | 51455 |
| rs540451542 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452097 | TTTGTATTTAACACT[C/T]TCCTTTAATTCAGCA | 51455 |
| rs540460245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99423014 | GGATTTATTTATTTA[A/G]TTACCCAACTTATAA | 51455 |
| rs540477334 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491504 | TGGCCAGGCTGGTCT[A/G]GAAGTCCTGACCTCA | 51455 |
| rs540494976 | in-del | -/ATTAACACAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99413005 | ACTAATAACAAGTTT[-/ATTAACACAA]AATACCCACCATTTA | 51455 |
| rs540504120 | snp | A/C/T | 0.000482068 | 0.015518 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439327 | TAAAGCAGGAAAAAA[A/C/T]TTTTGAGTTAATAAT | 51455 |
| rs540529048 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | REV1 | GRCh38.p7 | 2:99407608 | TTGATGCCTCTTGCC[C/T]GTTTCAAAGGCATCT | 51455 |
| rs540568026 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99447867 | CCGGGATTACAGGCA[A/C]AAGCCACCACTCCCA | 51455 |
| rs540636318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485048 | ATGTTACACAAAGCA[A/G]CAGCCCTTTGACTTT | 51455 |
| rs540637360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478592 | TTCAAGGTTGCAATA[A/G]ATCAGGGATTCCAAA | 51455 |
| rs540737565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404132 | TGTTACTGTCCCCCA[C/T]GCAGGATTATACATC | 51455 |
| rs540743249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440867 | CAACAGAAAGCCATA[C/T]ATTGGCAGGAAAATA | 51455 |
| rs540745814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99442227 | ATTGCACTCCAGCCT[C/T]GGCAACAAGAGCAAA | 51455 |
| rs540773197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485747 | TTTGCTCTAGACATC[C/T]ACAAAATGTATTTTT | 51455 |
| rs540780803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457360 | TCAAAATCCCAGCAA[C/G]GTATTTTGTGGATAA | 51455 |
| rs540791759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448419 | AGGTTTCAGATGACA[C/T]ATTTAAACTTAGGAA | 51455 |
| rs540813721 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433393 | CACAAAGCATAAATA[C/T]GTATCTGCAATTATG | 51455 |
| rs540879119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417984 | CTGACACTAATACAT[C/T]GTTTTAAGTTATATA | 51455 |
| rs540942410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426478 | GTAAAATATAGTACA[C/T]CTACTTATGTACTCA | 51455 |
| rs540972845 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440994 | ACATTTTTTAGGCAA[C/T]GGCATAAATGTATTA | 51455 |
| rs540978603 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490748 | CGGGCAGCATTGCGC[C/G]TGAGTATTTGTAAAC | 51455 |
| rs540982779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417242 | CCTCTCGGGCTCAAG[C/T]GATTCTTGTGCCTCA | 51455 |
| rs541000628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487722 | CACACCCATACATTC[C/T]TGAAAAGCAGAAAGA | 51455 |
| rs541021622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99459156 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 51455 |
| rs541042352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405659 | CAATGGCAGTCCACA[A/G]GAGGACTGCCTTTCA | 51455 |
| rs541048576 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99407110 | TTTTTTTTTTTTTGA[G/T]ACAGAGCCTCACTGT | 51455 |
| rs541049997 | snp | A/G | | | intron-variant, upstream-variant-2KB, stop-gained | REV1 | GRCh38.p7 | 2:99479713 | GGATCGCTTGAGCCT[A/G]GAAGGTCAAGGCTGC | 51455 |
| rs541083754 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99404098 | ATGGGAAGCAAAACA[C/T]TGAAACAGGGACTCA | 51455 |
| rs541156870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467101 | AAGGTAAATAAAGGA[A/G]TAAAGTGTATTTTAA | 51455 |
| rs541195424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473260 | GTAGTCCCAGCTACT[C/G]AGGAGGCTGAGGCAG | 51455 |
| rs541229670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480909 | TCAAGACACCAGAAG[C/T]CTTATTCAATGTAAC | 51455 |
| rs541231613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472557 | AGAAAAGAGTTTTTT[A/T]AAAAAGTAGTTCTGA | 51455 |
| rs541258748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410528 | CTGAAACCAAGTGCA[A/T]TAACCTAAGCTGAAT | 51455 |
| rs541346624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471570 | AAACTGGACTACATA[A/T]AAATTTAAAACTTCT | 51455 |
| rs541347475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435705 | CCTGATAATCGAATA[C/T]AGAAAATTTGGAAGA | 51455 |
| rs541387683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99451323 | CATTAACTTTCCATA[C/T]ACATACTCATAAAGT | 51455 |
| rs541403203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488723 | CCACAGGCTGATTTG[C/T]TACATACAGAACTCC | 51455 |
| rs541454234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404880 | GAAGCCTGAAGTACT[A/T]TGTGTAGTCTGGAAA | 51455 |
| rs541503285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458960 | ACACCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 51455 |
| rs541519049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457305 | ATAGTAAAGATGTCA[A/G]TTCTCCCCGAACTGA | 51455 |
| rs541542748 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425189 | CTTGTTTTAAGAAAC[A/G]TATATACAAACAGTT | 51455 |
| rs541545253 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99466324 | CTCGGCTCACAACCA[C/T]CTCCGCCTCCCGGGT | 51455 |
| rs541551062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419880 | CATATCTTGGTTTTA[C/T]AGAAGACTTATATAA | 51455 |
| rs541558020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456417 | GAAGGTGGATAAGGG[G/T]TTAGAGAGCGACTGG | 51455 |
| rs541562105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464530 | CATTGTTTTAGTCAA[G/T]GTTATCCTTCCAGGT | 51455 |
| rs541598562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463902 | GTGCTGGGATTACAG[A/G]TGTGAGCCACCACGC | 51455 |
| rs541600895 | snp | C/T | | | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404525 | TATTTGCAACAAGAC[C/T]GTCCCAACTGGTTGT | 51455 |
| rs541672050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427946 | GGTAAATTTATATTT[A/G]CCGTGGGTAAATATA | 51455 |
| rs541672109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99419358 | GCTGGGACTACAGGC[A/G]CCCACCACCATGCCC | 51455 |
| rs541726639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432563 | GCAAATATTCTGGTG[A/G]GCTCCTAATACGTGA | 51455 |
| rs541733718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427272 | GGTAGTGGGTCCTTA[C/G]AAAAGCACAAGAAAA | 51455 |
| rs541735090 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | REV1 | GRCh38.p7 | 2:99434859 | CTCAATTTTACGCAA[C/G]AGAAACTAAATACAT | 51455 |
| rs541767922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99449179 | CTGAGATGGGAGGGC[C/T]GCTTGAGCCTGGGAG | 51455 |
| rs541777179 | snp | C/T | 0.000121278 | 0.00778617 | intron-variant, synonymous-codon, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99424860 | TACATGGTAGGACAT[C/T]ACTCTGGGCAGGAGC | 51455 |
| rs541787924 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456291 | TAGGCACTGGAGATA[G/T]GGCAATGAACAAGAC | 51455 |
| rs541866762 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99473230 | AATATTAGCTGGGAG[G/T]GGTGGCGCATGCCTG | 51455 |
| rs541901532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419719 | AGGCAGTGAGGTTCA[C/T]GGTGTAGGTGTGGGC | 51455 |
| rs541974220 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99468616 | TTCCACATAACTTGA[A/T]GACCTTGAGGAATGT | 51455 |
| rs542064195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425653 | GTCTGGTGTTGAAAA[A/G]GGTAAATTTCAGGTA | 51455 |
| rs542120995 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99406994 | ATTACGGCTGGCTTA[C/G]TGACTAATCTTTCAA | 51455 |
| rs542141157 | snp | C/T | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99442885 | AAGAGTAATAATTTA[C/T]ACTATTTTTATGTAT | 51455 |
| rs542154323 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99478505 | TAGAGGAAGGAGGAA[A/G]AAGCCACTGATCTTC | 51455 |
| rs542219299 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99466142 | ATTTTTAGTAGAGAC[A/G]GCGTTTCACCATGTG | 51455 |
| rs542219335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458177 | GACTGGGAGAAAATA[C/T]CTGCAAACCACTTTT | 51455 |
| rs542244549 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428727 | TAGGCCAGGCACAGT[G/T]GCTCACGCCTGTAAT | 51455 |
| rs542250929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411151 | AAATTAGCCTGGCGT[A/G]GTGGCGGGTGCCTGT | 51455 |
| rs542276443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475307 | AAAGAGGCAAAGGTG[C/G]AGGAGAACAAAGGAA | 51455 |
| rs542318703 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480599 | CCACACAAGTCATTA[G/T]ATCTCTGAACTCACA | 51455 |
| rs542360741 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99427189 | TTCATCTCTGGGGGA[A/G]AAAAATTGCCATCAA | 51455 |
| rs542392262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480010 | AGATTTCAGGAAGAA[A/G]AAAAATTCATAATTA | 51455 |
| rs542589137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99474122 | TTTTAGTGTTCCTTT[A/G]ATTTTTAACATTCAA | 51455 |
| rs542594413 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490693 | GATTCGTGGCCTGCT[C/T]CCGCAGGGCACAGAC | 51455 |
| rs542622706 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466313 | AGTGGCACGATCTCG[A/G]CTCACAACCACCTCC | 51455 |
| rs542665404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481777 | GGGAGGCTGAGGCAG[A/G]AGGATCACTTTGGCC | 51455 |
| rs542675820 | in-del | -/ACTT | 0.00159617 | 0.0282053 | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400369 | TGTTGCAGACACAAA[-/ACTT]ACTTAATGATTCATT | 51455 |
| rs542708763 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99464450 | TGTTTTCAAAGCTTA[C/T]TTCCATAACTCAGAG | 51455 |
| rs542830458 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475228 | TGTGTCTGGTTTCCA[C/T]TGGCTGGAACGGGAC | 51455 |
| rs542837284 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488807 | TTATTCTCGGAGACT[A/C/G]AAGTGCCAAGTCCGG | 51455 |
| rs542896016 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99413469 | CAGAAATGTTACATG[C/G]TATCACACATACCAC | 51455 |
| rs542901865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451125 | CTTATAGAATAACAG[C/T]GAGAAGTATCAAATT | 51455 |
| rs542908129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421333 | GATTATCAACCATTT[A/G]CTTATATTTCCAGCA | 51455 |
| rs542974405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458937 | GTGGAGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 51455 |
| rs542980062 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99457700 | AGAAAAAAAAAAAAA[-/G]AGAGAGAGAGAGGCG | 51455 |
| rs542982178 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468832 | CATTAACTACTGTTA[C/T]AGTAATCTACTCTGC | 51455 |
| rs542998179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474759 | AGAAAAAAATCAGCC[A/G]AGCATGGTAGCAGGA | 51455 |
| rs543047720 | snp | C/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400097 | AGGCTTCCATGTTAG[C/T]GTAGCTTCTCTCCCA | 51455 |
| rs543056409 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99435753 | AAATCATAATTTTTT[A/T]AAAAAAGATTTTGTA | 51455 |
| rs543093126 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99444011 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 51455 |
| rs543111254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407355 | CAGGAGTTTGAAACC[A/G]GCCTGGCCAACATGG | 51455 |
| rs543189263 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459194 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTCAA | 51455 |
| rs543208602 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99458895 | TGGGTGTGACTATGA[A/G]AGAGTAACATGAAAG | 51455 |
| rs543246450 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437087 | AGGGCTCAAACAATC[C/T]TCCCGCCTCAGCCTC | 51455 |
| rs543262237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412486 | TCTCAAGTTCTCTAA[A/T]AACTGGCCTCCAAAG | 51455 |
| rs543265050 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99477142 | TCTTCTTTCTTACTT[C/T]TAGTAATGGAACACC | 51455 |
| rs543278811 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488579 | CTGGAGAATGATTCC[G/T]GGAAGAGGAACTTTA | 51455 |
| rs543279441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472796 | AAGTGCTAGCACGCA[C/T]GCCCTAAAAAAAGTT | 51455 |
| rs543287184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411123 | TGAAACCTCATCTCT[A/C]CTAAAAATGCAAAAA | 51455 |
| rs543307481 | snp | C/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431781 | TGGGTCCCTCCACGA[C/G]CGGAGTGAGTTGCTT | 51455 |
| rs543309317 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478907 | AGTGGTGATAATAGA[A/G]AAAAGGACAGTTCAG | 51455 |
| rs543322130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99420616 | TGTGCCCCTCCTCTC[A/G]GGAAATGGAAGTAAC | 51455 |
| rs543418879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488773 | TGGTTGGTCCTACCC[C/T]ACCTAAACAGGAAAT | 51455 |
| rs543488469 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | REV1 | GRCh38.p7 | 2:99416723 | TGAGGTCAGGAGACC[A/G]AGACAGAGGTGAAAC | 51455 |
| rs543502520 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432265 | TAAAGTTTCAAAAAG[G/T]ACTAAGGATGCTATT | 51455 |
| rs543541589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459870 | TGTTAACTGGGTTGG[A/C]AGGTATAGGGACTAC | 51455 |
| rs543557391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450476 | ATCCCAAGCAATATA[G/T]GTCCAAGTATTTAAA | 51455 |
| rs543619705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99474004 | GCAATTCGTGTTTAT[G/T]GCAGAAAATTGGAAA | 51455 |
| rs543753078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473389 | AAAAAAGAAAAGAAA[A/C]GAAAAGAAAAAAGAA | 51455 |
| rs543766810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465671 | GGCTAAATGAAACCC[C/T]TTGTAAAGTCAAAGC | 51455 |
| rs543772653 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99425009 | ATTATACATAATTAG[C/T]AAAATTCTATTTTAT | 51455 |
| rs543815382 | in-del | -/A | 0.470715 | 0.117409 | intron-variant | REV1 | GRCh38.p7 | 2:99486528 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 51455 |
| rs543889688 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99452219 | TGCTTGAGCTCAGGA[A/C]TTCAAGACCAGCCTG | 51455 |
| rs543932479 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463274 | CCTGTGATCCCAGCA[A/T]TTTGGGAGGCTGAGG | 51455 |
| rs544023771 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | REV1 | GRCh38.p7 | 2:99475698 | TCTCAAAAAAAAAAT[A/T]AATAGGCCAGGCACA | 51455 |
| rs544051996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99419982 | GGGAAAGGCACTGAG[A/G]AGTGGAAATATAAAG | 51455 |
| rs544053594 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99490022 | CGCGGTGGCTCTCCG[C/T]CCCTCCCCCTCCGGT | 51455 |
| rs544116330 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428086 | TCCCCAGCCAGCATT[A/C]ATCTTGGTGGGGGAC | 51455 |
| rs544200436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469611 | CTACACAAGACTTCC[A/T]CTTTCCATTCTCTCA | 51455 |
| rs544200700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461208 | CAATGATGCCTAATA[A/C]AACACTTAATTACAA | 51455 |
| rs544207690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476369 | GAGACCAGCCTGGCC[A/T]ACATGGTGAAACCCC | 51455 |
| rs544211986 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413669 | CCACCTAAAGGATAC[C/T]GATTAATTCTGTTGC | 51455 |
| rs544240944 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99423574 | TTAATATGGAATATA[G/T]CTACACTTTTAAATA | 51455 |
| rs544243353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99431531 | ACAGCCACAACCAAC[C/T]GTCTTTCCAAGGTGT | 51455 |
| rs544251158 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99449843 | ATATGACCTTGATAT[-/TG]TGTTTTTAAAAATTA | 51455 |
| rs544265223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477424 | AGAACTGTGGAACCC[C/G]TAAAACACTGAGGTG | 51455 |
| rs544319765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439648 | ACATTTCTCATGGCT[A/G]AAGAAAAACCCAAAA | 51455 |
| rs544395060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401807 | TTTGAGACAAGCTGT[C/T]GATCAGGCTGGAGCC | 51455 |
| rs544419709 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482680 | TTTAAGATATAAAAC[A/G]TTGTGTTTGCTTCGG | 51455 |
| rs544437405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447354 | ATTTTGTATTTTTAG[A/C]AGAGACAGGGTTTCA | 51455 |
| rs544437810 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99429299 | ATTATGGTTTCAGAT[C/T]ACTATAAGATAAAGA | 51455 |
| rs544460999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99437907 | CTTTCTAGGACAGAA[C/T]CATGAGCTTCTCTCT | 51455 |
| rs544471707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99408197 | TAGTACTAAAGTAGT[A/G]TGGAACTGTTTAAAA | 51455 |
| rs544486301 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401150 | AATTTAAAATTATAA[A/G]AACTCCGAGCATTAC | 51455 |
| rs544499518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437428 | GCAGAGTAAGGATTT[A/T]GATTCATGCTAAACT | 51455 |
| rs544574423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99454650 | CTCAGGAGGCTGAGG[C/T]AGGAAGATCCGTTGA | 51455 |
| rs544590237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413660 | GTTTGAGCCCCACCT[A/G]AAGGATACTGATTAA | 51455 |
| rs544601925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485543 | GAAGACACGAAGCCT[A/C]CAGCAAGTCCTTTCA | 51455 |
| rs544640379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99484833 | GTCCCACAGCAGACC[A/G]GTTATGACCTCGGGA | 51455 |
| rs544681644 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476024 | AAATGTGTATGATTC[C/T]ACACATCTAGTTTTA | 51455 |
| rs544741637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429231 | AATTATGAGGAAGAT[A/G]TATATATATGAGTGT | 51455 |
| rs544750501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455254 | TCTTCATTATTTCAT[C/T]TGAGTTTCACAATCT | 51455 |
| rs544810506 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491721 | TTTTGCTTGTTTTAA[A/G]TGTCTAAATGGCAGC | 51455 |
| rs544842401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99449051 | CTTTGGGAGGCCAAG[G/T]CTGGAGGACTGTTTG | 51455 |
| rs544855103 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99472550 | TTAAGAAGAAAAGAG[-/T]TTTTTTAAAAAAGTA | 51455 |
| rs544861300 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99489895 | GGCCCCGCCGCCGCC[A/G]GTGCCCTCGCCAGGG | 51455 |
| rs544927909 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99437007 | TTTTTTTTTTTTTTT[A/G]AGATAGGGTCTCACT | 51455 |
| rs545015898 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99464313 | ATGGAAATGACTGCA[G/T]TATTTTTGCTGATTA | 51455 |
| rs545024172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474824 | CGACAATCACTTGAA[C/G]GCGGTAGGCAGAGGT | 51455 |
| rs545047751 | in-del | -/AAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99454553 | GAAACTCCAGCTCAA[-/AAAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs545058143 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491753 | TTCCTGCACGATTGT[A/G]TTTCAATTTTCTTTT | 51455 |
| rs545079691 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99452439 | AAAAAAAAAAAAAGG[A/G]AAAGAAAAAAAAAGG | 51455 |
| rs545096329 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491538 | AATCCACCAGCCTTG[C/G]CATCCTAAAGTGCTA | 51455 |
| rs545112730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439439 | CAGAAAATTCTTATA[C/T]TGAATATTGACAATG | 51455 |
| rs545113180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428755 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGCGGAT | 51455 |
| rs545124537 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99485377 | GCACAGCTGGGTTAC[C/T]TTAAGTTCCAATTAA | 51455 |
| rs545148498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454097 | CAATGGCTCTATCAT[A/G]GCTCACTGTAACCTC | 51455 |
| rs545211429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99489202 | TTAGCGAACGGACAA[A/G]CAGCAAGGAAAAACA | 51455 |
| rs545309794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99422666 | ATGAAGCTGAGATAG[C/G]ATTTCCCAAGGGTGG | 51455 |
| rs545315862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407420 | AGCTGGGCGTGGTAG[C/T]GGGTGCCTGTACCCC | 51455 |
| rs545328307 | in-del | -/TGAC | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481879 | AAAAACAAAAAAATT[-/TGAC]TGGCCATTGTCTGAT | 51455 |
| rs545461240 | snp | A/T | 3.85713e-05 | 0.00439137 | intron-variant | REV1 | GRCh38.p7 | 2:99438543 | ACCAATAATAGCATA[A/T]GAGCAAAATGATCAA | 51455 |
| rs545491997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401864 | GCAGCCTCCACCTCC[C/T]AAGTAACTGGGACCA | 51455 |
| rs545519207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470849 | TGGCAAAACTGCTGG[C/T]GAGTGTACCCTTTCT | 51455 |
| rs545561084 | snp | A/G | 6.60775e-05 | 0.00574755 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408081 | AACATGTTTAGCATC[A/G]CCTTTCCAATTATTT | 51455 |
| rs545588523 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484571 | AAGACACATGATTCT[C/T]TGACTTATTTTTAAT | 51455 |
| rs545606454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99462749 | GTGACCAGAACATAA[C/T]GATGACCTCATAAAC | 51455 |
| rs545611294 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99471983 | TAAAATGGTGCAGCT[C/G]ATATGAGAAACAGTA | 51455 |
| rs545656838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99406670 | AAACAATTTCTAAAG[C/T]AGCTAGTGAGTGGTC | 51455 |
| rs545768085 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469236 | CGTAAGTTTTAGGTT[C/T]AGGGTCTGAACAAGA | 51455 |
| rs545778396 | snp | A/C | 8.24409e-05 | 0.00641979 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418930 | TAGTTGCCATTCTAG[A/C]CAGGAGAATATTAGA | 51455 |
| rs545778730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410618 | TCAAACTCCTCCTTG[A/G]TTTTCTTCATTTTCT | 51455 |
| rs545781521 | snp | G/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402708 | TTCAACAGCTCCAGC[G/T]AGATTGGGTGCTGGA | 51455 |
| rs545818117 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99405186 | GCTGAATTTTCTCTA[A/C]CTTACAGGACAGAAT | 51455 |
| rs545823796 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | REV1 | GRCh38.p7 | 2:99409858 | AAAACAAACAACCCC[C/G]CCCCCCCCCAAAAAA | 51455 |
| rs545861680 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428860 | AGCCGGGTGTGGTGG[C/T]GAGCACCTGTAGTCC | 51455 |
| rs545899891 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487319 | TTAGAGGACACTAAG[C/T]AAGAAAGTGACAATC | 51455 |
| rs545953656 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99459065 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGGCC | 51455 |
| rs546042651 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99431489 | AGGGTGCTACTAGAC[C/G]CCAAAAAAAGGAGTG | 51455 |
| rs546056222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478714 | CAGTAATTCTCACAC[A/G]TGAGCATGCATCAGA | 51455 |
| rs546066508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415542 | TGAACTTTCTGCAGT[A/G]ATGGAAATGTTCTCG | 51455 |
| rs546105608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99485841 | TAAAATTTAGCCAGA[C/T]ACAGTGGCTCACACT | 51455 |
| rs546184447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472418 | TTTAACAGGTAGAGT[C/T]TCAGGCAAGGTGAAG | 51455 |
| rs546230055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99446675 | AATTTTTGTATTTTT[A/C]GTAGAGACAGGCTTT | 51455 |
| rs546276631 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491200 | TGCACTTCAACTTCA[C/G]TATTCTCGTCGCTAA | 51455 |
| rs546281496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433886 | CAAGGTTATTTCTCA[G/T]AACAGGTTCACTAAA | 51455 |
| rs546318051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99479189 | AAAAATTAGCCAGGT[A/G]TGGTGGCACTCCCCT | 51455 |
| rs546391131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99407077 | ACTAAACCTACAAAG[A/G]TTCTTTTTTTTTTTT | 51455 |
| rs546480818 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400542 | AAATATTTTATATAC[G/T]TTTGAAAAATCTATA | 51455 |
| rs546481211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468474 | AATGTGTCCTCTTGA[C/G]TAAACCTACTCACTA | 51455 |
| rs546505612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413872 | GGTCTTCTGTAGGAA[A/C]TTATCAAAAGAGAAC | 51455 |
| rs546620406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475136 | AGAAAAGGTACACTC[A/G]CCAGCAGTTTTGCCA | 51455 |
| rs546625042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407648 | TGTGGTTTCACTCCC[C/T]TCTAGGTCATCATAC | 51455 |
| rs546630513 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99489221 | CAAGGAAAAACAAGG[C/G]AGCAACAACCGCCTT | 51455 |
| rs546683421 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99462213 | GGACCTACAGTGAAG[A/C]TCACAGTTTACAAGT | 51455 |
| rs546687241 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440582 | GATCATGCCAGTGAT[G/T]GGGAAAAAGACAAAG | 51455 |
| rs546688897 | snp | A/G/T | 0.000116393 | 0.00762786 | intron-variant | REV1 | GRCh38.p7 | 2:99424288 | CAAGTTGCCTAGAGC[A/G/T]AGAACAAAACACAAT | 51455 |
| rs546690066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414593 | TGGGTTTGTCAAAGG[C/T]AGACACTTTGCACAG | 51455 |
| rs546706037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408578 | AGATAAATTCTCTGT[A/G]TGTTGTTTCTTGACT | 51455 |
| rs546707869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454309 | AATCCCAGCACTTTG[A/G]TAGGCCACAGCGGGT | 51455 |
| rs546745986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461288 | TACTTAACTCCAATT[A/C]AACAAATATGTCCTG | 51455 |
| rs546784554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99460222 | GCTGGGACTACAGGC[A/G]CACGTCACCACGCCC | 51455 |
| rs546822516 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99469935 | GACCATACTGGCTAA[A/C]ACGGTGAAACCCCGT | 51455 |
| rs546860068 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99414661 | CTCTTTTTGTTATTT[A/C]TTTTTTGTCATAAGA | 51455 |
| rs546919425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420993 | CAGGGTAAGTGCTGG[C/G]AGCAGCTGTGGAAAC | 51455 |
| rs546926234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439738 | AGTTCTGAAGCACAG[G/T]GCTTGGCATTTACTA | 51455 |
| rs546939879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429322 | GATAAAGACCTATAC[A/T]AAAAGTTGGTGCTAA | 51455 |
| rs546965810 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99442898 | TATACTATTTTTATG[C/T]ATACAAGAATGGTTA | 51455 |
| rs546969049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444852 | TTACTATTTCCCCTC[C/T]TGTTCTAAGCGCAAA | 51455 |
| rs546997327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99416454 | GAAATGTTCTATAAC[A/C]GTCAGGTTAAGGATT | 51455 |
| rs547003126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478813 | GTCTAGGGCAGGGCT[A/G]GAAATTTGCATTTCC | 51455 |
| rs547015208 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433520 | TTTGCCTTAATTTCA[C/T]TGGAGTCATTGTGAC | 51455 |
| rs547042349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485991 | CTAGCCAGGCATGGT[A/G]GCACATGCCTGTAGT | 51455 |
| rs547054548 | in-del | -/CAA | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99489223 | GGAAAAACAAGGGAG[-/CAA]CAACAACCGCCTTCG | 51455 |
| rs547115047 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434272 | AACAACCATGCCAAA[C/G/T]AGCAAAATCCAGAAG | 51455 |
| rs547230617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484361 | AAACATTCATATGTA[C/T]CCCAGAACCTAAGAT | 51455 |
| rs547231360 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491759 | CACGATTGTATTTCA[A/G]TTTTCTTTTCCACTC | 51455 |
| rs547263559 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99429722 | TGATTAAGGCTAAAA[-/C]CCTCATAACACGTCT | 51455 |
| rs547269947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439826 | ATTTAAAAACCTTAC[C/T]TGAATTCTTATTCCT | 51455 |
| rs547280780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448118 | CCACGCTGCTTCTCC[G/T]TGAATTTATGCGGCT | 51455 |
| rs547314769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455859 | CCCTTGTTTCATTTT[A/G]TGAATTGTGCTAAAG | 51455 |
| rs547444490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433234 | CTAAGAAACTACCTA[C/T]ACCATAATACAAGTA | 51455 |
| rs547453532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426240 | CAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51455 |
| rs547476487 | in-del | -/ATTTTA | 0.00119737 | 0.0244387 | cds-indel, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400495 | TTTTAAACTATTTTT[-/ATTTTA]AAGTTATGGCATAAC | 51455 |
| rs547483121 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99441274 | AAAAATTACAGAAGG[C/G]AGTGATACTGGATCC | 51455 |
| rs547527578 | snp | A/G | 3.30518e-05 | 0.00406507 | intron-variant | REV1 | GRCh38.p7 | 2:99404394 | CCTAAGTTGGAGCAG[A/G]GGGGTGAGAATATTG | 51455 |
| rs547548998 | snp | G/T | | | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402651 | AAGCCAACCTGAAAT[G/T]GTAGTTATCCATTCT | 51455 |
| rs547554755 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99479244 | AGGCAGAAGAACTGC[C/T]TGAACCAGGGAGTCA | 51455 |
| rs547589172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411170 | GCGGGTGCCTGTAAT[C/T]GCAGCTACTCAGGAG | 51455 |
| rs547644730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99465893 | ACACCTTAAACCATG[A/G]CACTTTACCCCACAC | 51455 |
| rs547664502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99402076 | ACCTTGAGGGCAACA[C/T]ATTTGGAACCTTATT | 51455 |
| rs547684368 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99409367 | GTATGGTTGGCATGA[A/G]CTAATCTTTAATGAA | 51455 |
| rs547722346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443543 | AACAGATTCTAAAAA[C/T]GGAACTATATATGAT | 51455 |
| rs547759028 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99488261 | TTTGAAGTTGCGAGT[C/G]GGAAGTTGGAAATGT | 51455 |
| rs547777985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485931 | AGAGTTTGAGACCAG[A/C]CTGGGCAAAACAGTA | 51455 |
| rs547899347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450819 | CTCTGGAATCCAGTG[A/G]GTATTTTACATTTAC | 51455 |
| rs547937472 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99450100 | TAATATGAAATTTCA[G/T]TAAGGCCAAAAAATA | 51455 |
| rs547973827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457612 | ATCGCTTGAGCCAGG[A/G]AGGCAGAGGGTGCGG | 51455 |
| rs547974601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465064 | TATTTCAATATCAAG[A/G]AAATGAGAAATTAAA | 51455 |
| rs547996823 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410798 | GACGTTTACCCTTCA[C/T]GCCAGTGGCTTCTAG | 51455 |
| rs548054971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447672 | AGGCAGATATTAGCC[G/T]TCTTTCACAAATGAG | 51455 |
| rs548071122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418362 | TTTACGTTTCCTTTT[C/T]CCTAATACAGCTCAC | 51455 |
| rs548094629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455019 | CCCAGCTTATAGAAA[G/T]TTTTGCTCATCTGGT | 51455 |
| rs548122155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462145 | CACACCCACACACCA[C/T]CCCACCCTAAAGGAC | 51455 |
| rs548144703 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403982 | CTTCAAAATGGTTAG[A/G]GCAAGAATAAGGAAT | 51455 |
| rs548167101 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99441185 | TAGCACATTAAAAAA[A/T]ATTAAAAGCTACAGG | 51455 |
| rs548298243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448042 | ATATGGATACTGAAC[G/T]GCCGAGTTTGGAAGT | 51455 |
| rs548301860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440585 | CATGCCAGTGATGGG[A/G]AAAAAGACAAAGTAG | 51455 |
| rs548410959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418312 | GATGGAAGGTTTTTT[C/T]CCATGAGTGGAGTTA | 51455 |
| rs548446381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99401576 | ACATGGTAAAACCCC[A/G]TCTCTACAAAAAATA | 51455 |
| rs548450710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99409170 | CTATTTGAGATACAT[A/G]TGTATCATAACAGGT | 51455 |
| rs548458813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408392 | TTAGGTCAACTAAAA[A/G]TAAGTTGAGAAATTT | 51455 |
| rs548475924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471867 | TGAGATACCACCTCA[C/T]ACCCAGCAGGATAGC | 51455 |
| rs548481478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415575 | TGCTATCCAATACAG[A/G]AGAACCTTGCTCCAT | 51455 |
| rs548590713 | in-del | -/TTAATCTTGATCTGTT | 0.0256215 | 0.110247 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400210 | AGAGATTTTTATACA[-/TTAATCTTGATCTGTT]TTAATCTTGATCTGT | 51455 |
| rs548671421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427558 | CAGTGCATCAAACTG[A/G]GCAGATCATCCCCAC | 51455 |
| rs548680555 | snp | A/G | | | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402360 | ATCTAGGAAGGGGGA[A/G]AAACTTCAAATGAGG | 51455 |
| rs548686561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466524 | TAGGATTACAGGCAT[A/G]AGCCACCATGCCTGG | 51455 |
| rs548723897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473422 | AAATTCAGACACCTA[A/G]GTGAAGGGCACAATT | 51455 |
| rs548728429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435071 | TATTCTGAGGACCAA[C/G]AAATAAAATCAACAA | 51455 |
| rs548732222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420021 | TGGCATTACATATGC[C/T]TGAACTTAAAAGAAT | 51455 |
| rs548747688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456876 | ACAAACAGAAACACA[A/G]AACTGTAAAAGTAAA | 51455 |
| rs548785589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471234 | TCAATTCTCTGCTAA[C/G]GCATTTATTGACAAC | 51455 |
| rs548820219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478780 | TGGGCCCCAACTCCA[A/G]CGTTTCTGATTCAGT | 51455 |
| rs548864016 | snp | A/G | 6.60698e-05 | 0.00574722 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434426 | TCCTGTGCCTCTGTT[A/G]CTTGTAACAGCCACT | 51455 |
| rs548946220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482778 | ATTTACACTTTGGGA[G/T]GCCGAGGCAGGCGGG | 51455 |
| rs548950996 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456103 | AACATGCCCAGAGCC[G/T]ACCTCCCAGATTACA | 51455 |
| rs548976706 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437173 | TTTTTGGTAGAGACA[C/T]GGTCTCACTGTGTTG | 51455 |
| rs548981306 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482080 | CATGTGAATAGTGGG[C/T]TGGGCTTTGAGCAAC | 51455 |
| rs548985176 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490239 | TTCTGCAGCCGCCCG[C/T]AAGGGGCAGCGCCTG | 51455 |
| rs549004742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443447 | TTTAAAAAATAATCA[C/T]TTAAGAAATGACTGA | 51455 |
| rs549053365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419417 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG | 51455 |
| rs549056186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481218 | ACTAATGAATAATTA[C/T]GTACATCTAAAAGTA | 51455 |
| rs549057010 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99429327 | AGACCTATACAAAAA[C/G]TTGGTGCTAACAAGT | 51455 |
| rs549064397 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434542 | TTTTAAAAACATGCC[-/T]TTTTTTTCTTTAGCT | 51455 |
| rs549118693 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99489494 | GGGCGCGGAGGGAAG[A/G]GCCGCTGCGCCAGGG | 51455 |
| rs549173365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459293 | CCAGTTGTGACACTG[C/T]TTGCAAGTTTATTAC | 51455 |
| rs549178966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480245 | GGAGAACTGCTTGAG[C/T]CTGGGAGGTTAAGAC | 51455 |
| rs549208613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437118 | CCAAGTAGCTGAGAC[C/T]GCAGGTGCGTGCCAC | 51455 |
| rs549275643 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99441320 | ACTCCTGGTGTTTTC[A/G]AAAAAAAATATATCC | 51455 |
| rs549277522 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470314 | AATTCATTTTGAGTG[G/T]CTTTTAATCAGTCTT | 51455 |
| rs549339876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474509 | TTCACCAGGTAATCT[A/G]GCAACAGTCTGGATC | 51455 |
| rs549352800 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476787 | AAGGCTTGGGTGAGC[A/T]TCCCTGATAGGCAAT | 51455 |
| rs549352946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465218 | CTCTTATATTTAAAA[C/T]TCAATAGAAAAATAT | 51455 |
| rs549382215 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99409313 | AAGAGCAGTCGTCTC[-/A]ACGACTTAGCAATAT | 51455 |
| rs549444541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435018 | ACTATAAATTTGTAA[A/C]GCAATAGCAGGGATA | 51455 |
| rs549535200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480217 | GGCCACAGCTACTTG[A/G]GAGAGTGGGATGGGA | 51455 |
| rs549540452 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99431431 | TTCATCTAAGCTGAA[A/G]AACTGTAAGAATTTC | 51455 |
| rs549545104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427457 | TGACCCACATATACA[C/T]ATTCTACTTTGTATT | 51455 |
| rs549571001 | in-del | -/TGTT | | | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400436 | GAAGTCAGTGTGGGG[-/TGTT]TGTTTGTTTGAGGAA | 51455 |
| rs549579289 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461669 | AATTTAGGCAGAAAA[C/T]CTGGTAACTAACAGG | 51455 |
| rs549630340 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99457866 | ATCAATGGAAGAGAA[A/C]AGAGAACCCAGAAAC | 51455 |
| rs549665171 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99484960 | AGCTGTAGATATTAA[C/T]TAAGACACTGCACCT | 51455 |
| rs549667374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454885 | AGTAAAAGCCATATA[C/T]AAGGACCACAATTTA | 51455 |
| rs549690899 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481732 | AAATTAGCCAGGTGC[A/G]GTGGTGTGTGCCTGT | 51455 |
| rs549755241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489244 | ACCGCCTTCGGACAT[G/T]CCGACCGGTTCTGGG | 51455 |
| rs549780883 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403739 | CTGTTCTCGCCCTGC[C/T]TTTGTCTTTGATCAT | 51455 |
| rs549798949 | snp | C/T | 0.000660513 | 0.018161 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449365 | TTCTGGTCGAATTAC[C/T]TTTTCCCCCTTTAAT | 51455 |
| rs549834787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418557 | ATCATCCTCCCTTTT[A/C]ACATTGTTTCTTAGA | 51455 |
| rs550013442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99422859 | CTAGGGCTTCAATAC[C/G]CAGGACACAGGAGCA | 51455 |
| rs550040221 | snp | G/T | 0.00262376 | 0.0361247 | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99451430 | ACTGGATGAAGTTAA[G/T]AGGGCTCTTTGAAGT | 51455 |
| rs550077347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99458990 | AAGGTGGGCAGATCA[C/T]GAGGTCAGGAGATCA | 51455 |
| rs550154573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99444664 | CTACAGTAATGTTAG[C/T]GAAGTAATGTCAGTT | 51455 |
| rs550156631 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99436337 | AGGTGTCAGGCACTG[C/G]TGTTAAGAGGTTTAT | 51455 |
| rs550164540 | in-del | -/AAAC | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400885 | GCCTTTTAGTATAAT[-/AAAC]AAACAGTAGTTGCTT | 51455 |
| rs550221075 | snp | C/T | 5.65179e-05 | 0.00531562 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406100 | AGATCCACAGCAGCC[C/T]GAAATACTACAAAAA | 51455 |
| rs550228816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419375 | CCACCACCATGCCCG[G/T]CTAATTTTTCTGTAT | 51455 |
| rs550330020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443577 | GAGTATGTCCTTTAT[A/G]TAATTATGTCAATAT | 51455 |
| rs550347712 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491331 | GCTCTTTTGCCCAGG[C/G]TGGAGTGCAATGGCG | 51455 |
| rs550357738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458496 | TGGGAGTATAAAATA[C/T]TACAACCACTTTGGG | 51455 |
| rs550379143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405019 | TCAAATTAGATCCCA[C/T]CCCAGGGAGGGGTGA | 51455 |
| rs550394464 | snp | C/G/T | 3.29469e-05 | 0.00405864 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404478 | GCTATTAAATTTATT[C/G/T]CTGCGTCACTGTTCG | 51455 |
| rs550442365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99411988 | TCTGTAATCCCAGCA[C/T]TTTAGGAGGCTGAGG | 51455 |
| rs550524904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474294 | ACACAATAGTTGACT[A/T]CTAGGGTAGAGAAGC | 51455 |
| rs550532536 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411411 | TTTTCCTTTCTTTCC[-/T]TTTTTTTTTTTTTTG | 51455 |
| rs550534862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420894 | CAGAAGGTAATGAGT[A/G]GGTTAAGAAAGGAAG | 51455 |
| rs550561503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482077 | AACCATGTGAATAGT[C/G]GGTTGGGCTTTGAGC | 51455 |
| rs550579651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469272 | CTTGAAGAAAAAGCA[C/T]GACAACTTGAAAAAG | 51455 |
| rs550594446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428805 | CCATCCTGGCTAACA[C/T]GGTGAAATCCTGCCT | 51455 |
| rs550642809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99430978 | CCAGACAAATCTATT[G/T]TGAGTGCACTGTAAC | 51455 |
| rs550670643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421716 | TGGTAGACCCAATGT[G/T]GCAAAATAGTCTTCT | 51455 |
| rs550718608 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438798 | GAAGGTTTGGATGGC[A/T]CTGAAGGTGCTGCCT | 51455 |
| rs550752266 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460647 | GTGGTAAAGTATTCA[C/T]TAAAACTTAATTTTT | 51455 |
| rs550789420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423158 | CATTTTCTCTCTCTC[G/T]CCTACTAAAGCAAGC | 51455 |
| rs550858353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428572 | ACTTAATGCTTTTTA[A/G]CTTAAATATACTTTA | 51455 |
| rs550889733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483997 | AATTAAAAAAGCCTT[A/G]CAAGGAAATGTCAGA | 51455 |
| rs550928106 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414972 | ATCACCAAGTTAACC[A/G]TAATCAATCTAATCT | 51455 |
| rs550983374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424118 | CTAAAAGAAGGAAAA[A/C]ACAGACACAAAATGA | 51455 |
| rs551022437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99445506 | GAACAACAAAAACAA[A/G]AACAATCTGTAGCAA | 51455 |
| rs551024929 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99420841 | GGCAGGGACAAACTG[C/G]CTCTAGTAACAGAAT | 51455 |
| rs551086210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420116 | CCTGACAATGGAATA[C/T]AGAATTCCTAAGTGA | 51455 |
| rs551140241 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99406700 | ATTCATCTCAAACTT[-/AA]CAGAGTATCCAATTC | 51455 |
| rs551159233 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459722 | AAACAAAGAAACAAA[C/T]AAAACAAACAAAAAG | 51455 |
| rs551192594 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99403231 | CACCTCCCCTCCTGC[C/T]CCAAGTGAGAGGCAG | 51455 |
| rs551225593 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400518 | GTTATGGCATAACAT[A/G]TAACATAAAAATATT | 51455 |
| rs551260588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99427659 | AGGAAAATATAACCT[A/G]TTGGATGGCCACAAA | 51455 |
| rs551263152 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490418 | GCGCCGCTCCGTGCA[C/T]AGCGAGTCCCCGCGC | 51455 |
| rs551290709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454146 | TGTAATTTGAAAGAT[C/T]TGGGAGGCTGAGGCA | 51455 |
| rs551322953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428538 | GAAAACAGTTTAAAA[C/T]ATAAGCATGCACGTT | 51455 |
| rs551338139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476030 | GTATGATTCTACACA[C/T]CTAGTTTTAAAAACG | 51455 |
| rs551363842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99436084 | AGAATTGAGTACAGA[C/T]TATTTCTATCACCTC | 51455 |
| rs551375130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475226 | GCTGTGTCTGGTTTC[C/T]ATTGGCTGGAACGGG | 51455 |
| rs551404993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405362 | GCCCTTTCCCCTAGT[C/T]TTGCAGCCAGTATTT | 51455 |
| rs551412505 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427583 | CCCCACAATCTAGTC[C/T]CCACTCCAAACTCAG | 51455 |
| rs551415575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412066 | GTGAAACCACGTCTC[C/T]ACTAAAAGTACAAAA | 51455 |
| rs551492984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466696 | GGTTAAGTCCCAACA[A/G]AGAGACAAGATAATA | 51455 |
| rs551506222 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | REV1 | GRCh38.p7 | 2:99462697 | AAAAAAAAAAATTTT[A/T]AAAACTAAATAAATA | 51455 |
| rs551562894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429471 | AGGAAGTATGGATTA[C/T]AAGATTTTTTCTTAG | 51455 |
| rs551580776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473653 | GTGTTTTTTTTACAC[C/T]TTCAGCATACTGAAA | 51455 |
| rs551652896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480543 | TAGCCTACACCATAA[C/G]GTATAAATCTTAGCA | 51455 |
| rs551659722 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99465123 | AATATTAAGTAAACT[G/T]TTTCTGAAGTTCTCC | 51455 |
| rs551688008 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99452588 | ATCTGAAATTACCAT[A/G]TCTGTTTGTTTACTT | 51455 |
| rs551696417 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433843 | TTTTGCTTATTAATA[C/T]CCAAAATTAAAAAGT | 51455 |
| rs551750665 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438615 | CCTGTGTCAGTTACA[A/C]CAAGTGCAGACCTGC | 51455 |
| rs551975691 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | REV1 | GRCh38.p7 | 2:99489410 | CGCGGAACTGAATGG[A/C]CGGCCGAGGCGCCGG | 51455 |
| rs552052919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99454339 | TGGATCCTCTGAGGT[C/T]AGGAGTTCAAGACCA | 51455 |
| rs552073136 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400718 | TCCGCATGGAAGAAG[A/T]AGTAAAGATTTTCTT | 51455 |
| rs552156415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439882 | ATTCAACACATTAAA[C/T]CTAATACGAAACCAG | 51455 |
| rs552294878 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99447609 | ACATGCTAGGCACTG[C/T]ACCAGGTTGTATGGA | 51455 |
| rs552329719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99446877 | GTCCACAGAAATTCC[C/T]CATTCCCTCCAAAGC | 51455 |
| rs552332811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99402188 | ACAACTCAGTACACC[C/T]TCAGCCATTGTGACA | 51455 |
| rs552334168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408355 | AACACTAGAACTTTA[A/C]GGTAAAAACCGTAAT | 51455 |
| rs552412486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99425905 | GCGAGAAGTGGTGGC[A/G]CATGCCTGTAATCCC | 51455 |
| rs552443680 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419667 | CCCAAAGCAGCAGTG[C/G]GAACTGAGGGTAGAA | 51455 |
| rs552450847 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99476464 | AGGAAGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 51455 |
| rs552461236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414814 | AGGGACTTCCAAGAT[C/T]AGCAAGAGACAATCA | 51455 |
| rs552490546 | in-del | -/A | 0.487746 | 0.0773096 | intron-variant | REV1 | GRCh38.p7 | 2:99479327 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51455 |
| rs552503269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429040 | CTAAGACTCTGTTTC[A/G]ATTTGAAATTATTGA | 51455 |
| rs552522815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413982 | CAACTGAGGTAGACC[A/G]TCTCTATAAAATAGA | 51455 |
| rs552545099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464080 | TGGCTAAATTCTGGA[G/T]CTAATCAATCTATTT | 51455 |
| rs552567805 | snp | A/G | 6.7706e-05 | 0.00581794 | intron-variant | REV1 | GRCh38.p7 | 2:99408170 | CAAAAGCTTCATTCC[A/G]TATGTATTCACTAGT | 51455 |
| rs552744017 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | REV1 | GRCh38.p7 | 2:99471141 | AGGCAAGGTTGAAAC[A/T]CAATTTGCCTTTGGT | 51455 |
| rs552745938 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422135 | CACAGTTAAATTCCA[C/T]TCACTGTAGCAGGCC | 51455 |
| rs552771588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425170 | ACACAGCATGGAGAC[A/G]TGCCTTGTTTTAAGA | 51455 |
| rs552789172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470564 | GCCCCGGCAAGCTTA[C/T]ACTGGTCCAAGCAAG | 51455 |
| rs552795356 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486267 | GGGACCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 51455 |
| rs552814531 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431910 | AGAATGTGGAGGAAC[C/G]GTTGGAGAAATCAGA | 51455 |
| rs552827888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477968 | CTAGGCACAGTGGCT[C/T]ACACCTGTAATCCCA | 51455 |
| rs552866630 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99476975 | TCCAACCATAAGTAA[A/C]AGCCCTTTCAGGAGT | 51455 |
| rs552885474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99437831 | TTTGACTAAAAGCAC[A/G]TAGGAATACATCAAA | 51455 |
| rs552912787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455097 | TCCTAGCTAGATCTC[C/T]ATTGAGAAAACATTT | 51455 |
| rs552921708 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440491 | ATGATCACCCATTTC[C/T]GGGTTAGCTCAGGCT | 51455 |
| rs552927086 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410215 | GGAGTTTCACCATGT[C/T]GGCCAGGCTGGTCTC | 51455 |
| rs552942867 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99485167 | TTTTACTAAGGACAA[A/G]TGAATTTAAAATAAC | 51455 |
| rs552967484 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490503 | GGGCTTCAAACCCCG[C/G]TACTGTGTGAAGATG | 51455 |
| rs552995345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483146 | GGCTTAAAATAAAAA[C/G]CTAAGGAGTCATCAA | 51455 |
| rs553030419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482444 | GAAAGTTGTAGCCAG[C/T]TGGTCAGAGTGTGGA | 51455 |
| rs553077297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489530 | CGCGGGGCGGCCCAT[A/G]GGGCTGGCGGCGGCG | 51455 |
| rs553107268 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436046 | ACATGCTTACACCCA[A/G]AATGGAGTCTTTTTA | 51455 |
| rs553110081 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99438452 | AATAAATTAGCTTTC[-/TA]TGTTATGCTTACTGT | 51455 |
| rs553155407 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447900 | TAATTGTATTTTTAG[G/T]ACAGACAGGGTTTCA | 51455 |
| rs553169033 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99453109 | CTCACACCTGTAATC[C/T]CAGCACTCTGGGAGG | 51455 |
| rs553195466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468277 | GACTCCGCCAATGCC[A/T]CTGTAATAACATCCA | 51455 |
| rs553204161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451931 | TTGGCATGCATGGTC[A/G]CTGGAAGCTACCCTA | 51455 |
| rs553208267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459675 | AGTGCCACTGCACTA[C/T]AGCCTGGGTGACAGA | 51455 |
| rs553247448 | snp | C/T | 0.000131891 | 0.00811962 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401340 | AACCGATTCCACCGA[C/T]TGCTGCATCAGCCTA | 51455 |
| rs553273953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99467856 | TTGGAGACCAGTCTG[A/G]CCAACATGGTGAAAT | 51455 |
| rs553341981 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99465937 | ATTTCTTTCTTTCTT[-/TTTA]TTTATTTATTATTTT | 51455 |
| rs553382884 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99455722 | AAAATTAGACTTGTC[A/G]ACACTAAAGAGAATC | 51455 |
| rs553384778 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419527 | CAGTCCTGATCTTCA[C/G]AGTGGGTGTCTGTAG | 51455 |
| rs553403470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478358 | TCCAAACCACATGGC[C/G]CAATTGCATTTATTA | 51455 |
| rs553432144 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401047 | GAATCTATGCTACAG[C/T]AAAATAATTAACACA | 51455 |
| rs553435532 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439379 | AATTTTTTCATTTCA[C/T]CATTTTCTTAGTGGT | 51455 |
| rs553472590 | in-del | -/A | 0.293551 | 0.246177 | intron-variant | REV1 | GRCh38.p7 | 2:99451773 | GCCCTAGACTCTACG[-/A]AAAAAAAAAATGACA | 51455 |
| rs553476167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99461795 | GAGAAAGTCATGAAA[C/T]AAACACACAGGCACC | 51455 |
| rs553539362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470276 | CATATCTGTAACTCT[A/G]AAGTCTGTTGATTAA | 51455 |
| rs553540104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485297 | CTCCATCAATTCTTT[C/T]TTCTCTTATTTCTGT | 51455 |
| rs553576911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484681 | TTAAGTATAGTAGTA[G/T]TAGTTAAATCTAAAA | 51455 |
| rs553675726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447747 | TTTTTCCTGAGACGG[A/C]GTCTTTCTCTGTTGC | 51455 |
| rs553741681 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99470720 | AAGTTGCTAGCCAAT[C/G]AGAACAAATACAGAA | 51455 |
| rs553808046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439363 | ACTTTTAGGTTAAAA[C/G]AATTTTTTCATTTCA | 51455 |
| rs553838791 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459015 | AGATCAAGACCATAC[C/T]GGCTAACACGGTGAA | 51455 |
| rs553840300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416971 | GAAGCAAATGAAGGT[A/G]AATGGTAGGATTACT | 51455 |
| rs553883281 | in-del | -/AA/AAAAA | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99401772 | AATCCTAGAACACTC[-/AA/AAAAA]AAATTTTTTTTTATT | 51455 |
| rs553884495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431385 | GTTTCTGGAGGGTTT[C/T]AAAAGGGTAAATATA | 51455 |
| rs553903197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487175 | ACCGGCAAAATGACT[A/G]TGGGACTGGGGTAGG | 51455 |
| rs553903681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99425366 | GTGCTAAGTCCCTAG[C/T]AGATAAGAAATACCT | 51455 |
| rs553909018 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487181 | AAAATGACTATGGGA[C/G]TGGGGTAGGTTGCTG | 51455 |
| rs553915626 | snp | C/T | 0.00214146 | 0.0326519 | intron-variant | REV1 | GRCh38.p7 | 2:99424735 | CTACACAAAACAGTG[C/T]TATGTGACAAACAGA | 51455 |
| rs554092839 | snp | A/C | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490329 | GCACTGCGCCGCCTG[A/C]CCGCCCGTCCTGCTC | 51455 |
| rs554123559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401640 | TAATCCCAGCTACCC[A/G]GGAGGCTGAGGCAGG | 51455 |
| rs554130507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410213 | ATGGAGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 51455 |
| rs554197357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479929 | CTGAACTAAGAACAA[C/T]CAGTAGGATTTTACA | 51455 |
| rs554200250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484610 | AATATGAGAAAAACA[A/T]TAATTACGATGCAAG | 51455 |
| rs554205974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464418 | GTATAATCCTATTCA[A/T]TAAAACTTTGGGGTG | 51455 |
| rs554213348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99486306 | AGGCTGAGGCGGGCG[A/G]ATCACGAGGTCAGGA | 51455 |
| rs554231475 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433747 | TTTCTAAGAAAACAT[A/T]TCTCAGTGAATTTAC | 51455 |
| rs554242422 | in-del | -/ATT | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99446004 | GTATAATAAAATCTC[-/ATT]AAAACACAGCTAAGA | 51455 |
| rs554244393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99479157 | ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA | 51455 |
| rs554270587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99441888 | TCAACATGTTTATTA[C/T]AAGTGAATGGCCAGG | 51455 |
| rs554337233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484177 | GCAGCCAAATGATGA[A/G]AACTCATGAACGCAA | 51455 |
| rs554374956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99449015 | ATAGAAAGGCCATGC[A/G]CAGTGGTTGTAGTCC | 51455 |
| rs554403625 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434880 | CTAAATACATATGCA[C/T]AGGAATCACAATCTG | 51455 |
| rs554405541 | snp | C/G | 3.3516e-05 | 0.00409352 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402613 | ACGACTACATCTCAG[C/G]CTTGGGCCATCTAAC | 51455 |
| rs554470597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99409792 | AAGTTGCAATGAGCC[A/G]AGATCGCACCACTGC | 51455 |
| rs554515757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424483 | ATAGTGTAAATGACA[A/C]ATGTAGATGTGCCAA | 51455 |
| rs554517286 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432663 | ATCTTTTTCTAGTGA[A/C/T]GGGACAATCTCCTTT | 51455 |
| rs554582922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477164 | TGGAACACCTCTCCC[A/G]CCCCTCTTAGCAGGA | 51455 |
| rs554584326 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400066 | AACAGACATCCACCA[A/G]TAAGCAAGCTCTGTT | 51455 |
| rs554588281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471746 | AAGAAATAAAAAAAG[A/G]ATCTGAACAGACACT | 51455 |
| rs554617036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445952 | CAGAAGAGTATGTAA[C/T]GTTTATTAAATAGCT | 51455 |
| rs554618559 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99453589 | TACTAGCAAAGAATA[A/C]ACAGAAAATAAAAAA | 51455 |
| rs554660516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402447 | TTCTACAACTATGTC[A/G]CTAACAGCTATCAAA | 51455 |
| rs554675738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448924 | AACATGAGCTTAAAC[A/G]GTAGTGTTGTTTAAG | 51455 |
| rs554702576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431283 | AACAGCAGAGTGTGT[A/G]ATGTGAGCTAGTTTC | 51455 |
| rs554739629 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99430639 | GAGAACACAACTGGA[G/T]CCTAGTGTGGCTTAC | 51455 |
| rs554741336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440102 | TAGATGCCAGGGTGG[C/T]ACAAGGCAATCTGGA | 51455 |
| rs554760902 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447034 | ATACTATATCATTGA[A/G/T]AGACAGTGGTTAGGT | 51455 |
| rs554772924 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99409702 | TACAAAAATTCGCTG[C/G]GCATGGTGGCATGCC | 51455 |
| rs554835765 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99445324 | AAGAAAAGATAAACT[C/G]AAAGTCCTACTAGTA | 51455 |
| rs554858164 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99400968 | ATACAGTTCTTTATT[A/G]AACAACTGTAAACAC | 51455 |
| rs554927963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458590 | CTCTTCTTATACTCA[C/T]ACAAAAACTCATACA | 51455 |
| rs554955790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416855 | AAGGCAGAGCTTGCA[C/G]TGAGCCGAGATCGCA | 51455 |
| rs554960406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440794 | ACGTCAGAAAGTCTT[A/C]CATCTAGTTTTGTGT | 51455 |
| rs554995487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486142 | AAAATGTTAAAAAAG[A/T]AAAAAATTCAATTAA | 51455 |
| rs555083812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465448 | AGCCTGATTCACATA[C/T]TCTGCCAAAGCCCTA | 51455 |
| rs555093023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448280 | TACACTGATTATAAT[C/G]TATCCATACATAAAA | 51455 |
| rs555112233 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415188 | GTTTTAACTAAATAC[A/G]TCAATTAAGTAGGTG | 51455 |
| rs555172254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99418705 | TTTTCATGGCACTCA[A/G]TAAGACTTAAAAATT | 51455 |
| rs555187495 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99456063 | CTGAAGCACTCACTC[C/T]CCCTGGGCAGCTTTC | 51455 |
| rs555189245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99475503 | TATTTCTAATCAGAT[A/G]GGGAGGAAAGTCTTT | 51455 |
| rs555224397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455265 | TCATTTGAGTTTCAC[A/C]ATCTTATGAATTAGA | 51455 |
| rs555261191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462435 | TAGAATTTTAAAACA[A/C]ATCATTCTCAATCCT | 51455 |
| rs555277962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433634 | TAACTTCTGACTACT[G/T]TCTGGGTAATATATT | 51455 |
| rs555307719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450330 | TATTATGGCCTGCAT[C/T]ACTAGCATCACATTA | 51455 |
| rs555318970 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490675 | GCGCCACGGCGTTTT[C/T]GGGATTCGTGGCCTG | 51455 |
| rs555378773 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99465283 | ACTTACATAAAACAC[A/C]AAATCCAACTAACAT | 51455 |
| rs555378900 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436267 | CATGCAATCTACAAA[C/T]GCGCCTGGATAAAAT | 51455 |
| rs555397017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481525 | TTTAGCTGTCATAAA[C/T]TGAGCAAGTGTCTGT | 51455 |
| rs555437754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420290 | GGGAGAGACTGCCCT[C/T]CCAGGGCTGGCTAAT | 51455 |
| rs555440626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410483 | AAGGTCAGCAATGCC[A/G]TCAAACCAACCTCCT | 51455 |
| rs555457801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467019 | GTAAAGAGTTTGGGA[C/G]TTCTGGCCATTATAC | 51455 |
| rs555472058 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403928 | TTTTCTGATCTGTAC[A/G]AATTCTTAACAGTTC | 51455 |
| rs555503430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417975 | TACACATTTCTGACA[A/C]TAATACATCGTTTTA | 51455 |
| rs555533050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480734 | TCCAGCATTCACAAA[C/T]CCCTTTTCTCACAAA | 51455 |
| rs555554335 | snp | A/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490709 | CCGCAGGGCACAGAC[A/T]CTATCTTCTGTCCTT | 51455 |
| rs555569767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488663 | GTCCCTGCACGGGCA[A/G]ACCCAAGAATATGTG | 51455 |
| rs555593140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99479071 | ACAGTTGCTCATACC[C/T]GTAATCCCAGCACTT | 51455 |
| rs555611805 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | REV1 | GRCh38.p7 | 2:99422310 | AAAAAGGAAGACAAG[-/A]AGTTGCTATGTGGCC | 51455 |
| rs555704394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466336 | CCACCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 51455 |
| rs555729859 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99451313 | GTCAAGAACACATTA[A/T]CTTTCCATATACATA | 51455 |
| rs555766608 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477690 | AAATGTATAACAAAC[A/G]TTTGTATGTCCCAGT | 51455 |
| rs555775017 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99448916 | GTATTATCAACATGA[G/T]CTTAAACGGTAGTGT | 51455 |
| rs555801409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471405 | AAAAGAAGTTGGACC[G/T]TTACACCATGTTAAA | 51455 |
| rs555827355 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448060 | CGAGTTTGGAAGTTC[C/T]GAAGCCAAGTATGTC | 51455 |
| rs555864646 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475010 | ATATTTTAGTTCCTC[C/T]GTATGTGGAAAGAGT | 51455 |
| rs555877839 | in-del | -/CGGCCCCGCCCACGCCCCCTCCG | 0.487368 | 0.0784625 | upstream-variant-2KB, intron-variant | REV1 | GRCh38.p7 | 2:99490085 | TCCGCGCGCGCTCCC[-/CGGCCCCGCCCACGCCCCCTCCG]CGGCCCCGCTCGCGC | 51455 |
| rs555932847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99436397 | TATGAGGTAGGTAAT[C/T]GTATCATCTCCATCT | 51455 |
| rs555934453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470850 | GGCAAAACTGCTGGC[A/G]AGTGTACCCTTTCTG | 51455 |
| rs555934817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427918 | AGGCATGAAGCTTGA[C/T]CAAATTTATAAAGGT | 51455 |
| rs555971557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435426 | TATCCTACAATCAAA[A/C]AGTTGGGATGTTCAT | 51455 |
| rs555992470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99426302 | CAGCGAGCCAAGATC[A/G]TGCCATTGCACCTCA | 51455 |
| rs556082616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478941 | TAACGAGAAAGGTTA[C/T]ATACAGTAGAGAGAA | 51455 |
| rs556087974 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99434917 | CACATTATCAAACAT[A/G]AGCATACAGCCCCTC | 51455 |
| rs556106002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457237 | ATATATCTGTTCAAT[A/C]AACTAAAGAAAAATA | 51455 |
| rs556114424 | snp | C/T | 9.88338e-05 | 0.00702902 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404551 | GTTGTGGCAAAATTC[C/T]TGTATTACAGCCATT | 51455 |
| rs556122142 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415911 | CAAACTGTAATAGTC[A/G]TTGGGGTCAATCCTT | 51455 |
| rs556186884 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419284 | TGGTTGTGATCTCAG[C/G]TCACTGCAAGTTCCG | 51455 |
| rs556193001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484743 | GAAGCTGCCAGTAGT[C/T]AACAACACACACTCA | 51455 |
| rs556215531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431490 | GGGTGCTACTAGACC[C/T]CAAAAAAAGGAGTGC | 51455 |
| rs556228901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410347 | TACATTGAAATTTTC[C/T]TCAGGAAAAAAGTTT | 51455 |
| rs556288079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417813 | TACATGCAACTTTAA[A/G]TATACCAGTTCCTTC | 51455 |
| rs556289774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99409859 | AAACAAACAACCCCC[A/C]CCCCCCCCAAAAAAA | 51455 |
| rs556301939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417047 | ACTACAAAAAGGGTT[C/T]GATTTAAAGATGGTG | 51455 |
| rs556354090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488363 | TTTAAAAGAGCAATT[C/T]CCATCTTTACAAAAA | 51455 |
| rs556355966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478457 | GGAACACAAAAGAAT[A/G]TTCTAGAGATGACAT | 51455 |
| rs556394665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485363 | CAGAAAGATACAGAG[A/C]ACAGCTGGGTTACTT | 51455 |
| rs556486311 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99450230 | TATATGTCTTAAATA[C/T]TGGAAATATTTTAAG | 51455 |
| rs556490473 | snp | C/T | 1.66175e-05 | 0.00288244 | intron-variant | REV1 | GRCh38.p7 | 2:99418969 | AAAAAAAAAGTCATC[C/T]AAGAAATAGTCACAA | 51455 |
| rs556509739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99436699 | GAGATTCATCAGGGT[C/G]ATTTTAACCCTAATC | 51455 |
| rs556600987 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99427186 | GACTTCATCTCTGGG[A/G]GAAAAAAATTGCCAT | 51455 |
| rs556625814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487519 | GAGCCTGCAACCTAA[C/T]TGCCTCTAAAGAGCC | 51455 |
| rs556626153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472487 | TGTGAATGTACTTAA[C/T]GTGACTGAACAGTTA | 51455 |
| rs556628782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99457700 | AAGAAAAAAAAAAAA[A/G]AGAGAGAGAGAGGCG | 51455 |
| rs556653829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99405484 | ACCAGCAGTATATCA[A/C]ATGTACAGCCCACAC | 51455 |
| rs556728276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434742 | TTTGATTTCGTACTG[C/T]AGGAAAGAGGCAACT | 51455 |
| rs556799862 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99471326 | AGAACCTCTTCATGA[C/T]CATTCAATGAGGAAA | 51455 |
| rs556804131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99442081 | AGATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 51455 |
| rs556829400 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411772 | TAACTATGTTAATAA[A/C/G]TTCTGCTAATAAAAT | 51455 |
| rs556838067 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99403426 | AGGACAACTAGCTGA[A/G]CAAGTATTTAAGACA | 51455 |
| rs556860490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99449062 | CAAGGCTGGAGGACT[A/G]TTTGAGTTTGAGACC | 51455 |
| rs556919417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99461652 | CCAAGAAAATAGAGA[A/G]AAATTTAGGCAGAAA | 51455 |
| rs556994926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468751 | AGTTTAAAAAACGGA[C/T]GAAGAGTGAATACAT | 51455 |
| rs557065488 | snp | A/C | 0.271162 | 0.249103 | intron-variant | REV1 | GRCh38.p7 | 2:99453929 | AAATCAAAATAAAAC[A/C]AAACTAGATTCAGGG | 51455 |
| rs557078882 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484051 | CATCCCACCTATGTG[G/T]TCCTCCTTATTGAAG | 51455 |
| rs557104988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99451114 | ACCTGGCTGATCTTA[C/T]AGAATAACAGTGAGA | 51455 |
| rs557175901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445083 | AAATATTCATCTATT[C/T]TGGGAAGTCTTACTC | 51455 |
| rs557178557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473744 | CTATCTTGATAAACA[C/G]AGAATTCAAAGAACT | 51455 |
| rs557220476 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468459 | AACCTCCTGAATTAC[A/G]ATGTGTCCTCTTGAC | 51455 |
| rs557239566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421242 | TGGGAAAAAAAAAAC[G/T]GTTTACAAATGTTGA | 51455 |
| rs557249106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99466125 | ATTTTTCTTTTTTTT[A/G]TATTTTTAGTAGAGA | 51455 |
| rs557299548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451724 | ATGATCACACTAGAA[C/T]TCCTTTCGAGTAATG | 51455 |
| rs557302932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474736 | GTGAAACCCTGTCTC[C/T]ATTAAAAAGAAAAAA | 51455 |
| rs557308087 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466231 | GCTGGGATTACAGGC[A/G]TAAGCCACCGTGCCC | 51455 |
| rs557334482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451038 | TAATGTGAAACAGTA[C/G]AAATTAAACAGCTAG | 51455 |
| rs557339047 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448751 | GAACACTGCCTAGTC[C/T]TTAAGAGGTGCACAC | 51455 |
| rs557366615 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99428984 | GTGACAGAGCGAGAC[G/T]CCGTCTCAAAAAAAA | 51455 |
| rs557417787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414023 | AGCTGGGTGTGGTGG[G/T]GCGCTCCTGTAGTCC | 51455 |
| rs557431914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99422353 | CGAGGACTAAGAAAT[C/T]ACAAAATAGAACTGG | 51455 |
| rs557496012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413264 | CCAAGATATGTATCT[C/T]AGTCACAAAATCAAC | 51455 |
| rs557564376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483073 | AGATATTGAAGAAGA[A/C]ATTGTTAAAACATTT | 51455 |
| rs557588203 | in-del | -/ATTTTT | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99450020 | CTAGAAAGCTTTATA[-/ATTTTT]ATTTTTATTTAAGAA | 51455 |
| rs557592405 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99411651 | TGACCTCAGGTGATC[A/G]GCCTGCCTCAGCCTC | 51455 |
| rs557640831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427106 | AGAACGGCTTCAACC[C/T]GGGAGGCAGGGGTTG | 51455 |
| rs557645450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466098 | AGGTGCCCGCCACCA[A/C]GCCCGATTATTATTT | 51455 |
| rs557718759 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463603 | TAAACCAATTACAAA[-/T]TTGACAAGTGGTCTC | 51455 |
| rs557738902 | snp | A/C | 0.000363217 | 0.0134713 | intron-variant | REV1 | GRCh38.p7 | 2:99442270 | AAAAAAAAAAAAAAA[A/C]AAAAAACCAACCAGC | 51455 |
| rs557837274 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99419960 | AAAGTAGTGAGTTCA[-/G]GGGGAGGGGAAAGGC | 51455 |
| rs557839701 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99458934 | AGTGTGGAGGCCGGG[C/T]GCGGTGGCTCACACC | 51455 |
| rs557852308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459831 | TGAACTATTAGAGGG[C/T]CTTCCCTCCAAGTTC | 51455 |
| rs557854816 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99431274 | TTGCTTCAAAACAGC[A/G]GAGTGTGTAATGTGA | 51455 |
| rs557858378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404142 | CCCCATGCAGGATTA[A/T]ACATCTCCGCTCTGT | 51455 |
| rs557913710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457898 | GATCCACCAAAATAT[C/G]CCTAACTGACTGTGT | 51455 |
| rs557948372 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99465545 | TCATTCTCCTTAAGG[A/C]AACACTTACTTAACT | 51455 |
| rs557969023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99411086 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 51455 |
| rs558035661 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472389 | CAGAATGGTGGTTGC[A/C/G]GGTGGAGTTACTGTT | 51455 |
| rs558040385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428675 | GATTAGATGCCTGAA[G/T]AGCCACAACTCTGAA | 51455 |
| rs558190547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467168 | GTGTAACGTCTGTTG[C/T]ATACCTACTGCACAA | 51455 |
| rs558247663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428964 | GCCACTGCACTCCAG[C/G]CTGGGTGACAGAGCG | 51455 |
| rs558278484 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99412181 | GAGGTTGCAGTGAGC[A/C/G]GAGACTGCGCCACTG | 51455 |
| rs558278787 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99421154 | AAGTGCAGAGAGTAA[A/C]AAGACTCAGACTTAA | 51455 |
| rs558292869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420526 | GCTCTGGAGCCTAGG[C/T]GCTCCGTCTGCCACT | 51455 |
| rs558329511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482151 | ACTGGGGACTGAGTT[C/T]AATCATACCTATGTA | 51455 |
| rs558330255 | snp | C/G | | | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404509 | ATTCTTGAGGTTCTG[C/G]TATTTGCAACAAGAC | 51455 |
| rs558361733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429747 | ACGTCTGTAACATTT[A/G]AATCCACTTCAAAAG | 51455 |
| rs558371800 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490560 | AGCAATTGATTTACA[A/G]TGACATCTAGTGGAG | 51455 |
| rs558399577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437872 | CATAACAGAAAACAC[C/T]CCACATAGAGTCTCT | 51455 |
| rs558438222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99488740 | ACATACAGAACTCCA[C/T]AGAAAGAACCAAGGT | 51455 |
| rs558460444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435723 | AAAATTTGGAAGAAC[C/G]GATTTTCCCAAGGAA | 51455 |
| rs558538081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447806 | CTCACTGGAGCCTCC[C/T]ATCTCCTGGGTTCAC | 51455 |
| rs558559098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484142 | GAACACCAAACACCA[C/T]ATGTTCTCACTTGCA | 51455 |
| rs558621917 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99475693 | CTCTGTCTCAAAAAA[A/T]AAATAAATAGGCCAG | 51455 |
| rs558699671 | in-del | -/AAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99454584 | AAAAAAAAAAAAAAA[-/AAAAAAA]ACCCAAAAATTACGT | 51455 |
| rs558720668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453825 | TTGAACCTGGGAGGC[A/G]GAGGTTACAGTGAGC | 51455 |
| rs558752701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445782 | TGAAAGGATTCCCTT[A/G]CCTCTTCAAAGTCAG | 51455 |
| rs558760471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415740 | ATGCCTACATGATCA[C/T]GGTGGTTCTCTGAAA | 51455 |
| rs558764933 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418194 | CACTATAAATGAAGA[C/T]GGAAGACTTTACAAA | 51455 |
| rs558777885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407245 | GAGGCATGCACCACC[A/G]CACCCGGCTAATTTT | 51455 |
| rs558794096 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99445169 | GGCAAAAAAAACTCA[C/T]GAGAGATAAAATTGC | 51455 |
| rs558803639 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401134 | CACTTGCTTTAAAAG[A/G]AATTTAAAATTATAA | 51455 |
| rs558818732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99415118 | CAACTCCTATTGAGT[G/T]GGGGTGGGAAAATTA | 51455 |
| rs558851748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99460758 | TATAATGAAATCTTA[A/G]TAACAAGAGCAAAAA | 51455 |
| rs558868659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454603 | AAAACCCAAAAATTA[C/T]GTGTGGTGGCACACA | 51455 |
| rs558876747 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456462 | CTGTTTTAGATAGGT[C/G]AAGTCAGGGAAGGTC | 51455 |
| rs558919507 | snp | C/T | 1.65173e-05 | 0.00287374 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408086 | GTTTAGCATCGCCTT[C/T]CCAATTATTTTTGCA | 51455 |
| rs559070129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428364 | TAAAAAGCAGTATAA[A/C]AATTCAAAACGTATT | 51455 |
| rs559111434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474172 | CACATTACTAGTAAT[A/C]CCTTTCACTTCTGAA | 51455 |
| rs559113250 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99436998 | TTTTTTTGTTTTTTT[G/T]TTTTTTTTGAGATAG | 51455 |
| rs559152072 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433440 | ACCACATAAACAGAT[G/T]ATCAAAACCAACAAA | 51455 |
| rs559155805 | snp | C/T | | | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479896 | AGACACCCAAGAAAG[C/T]ATCACTGAGAGGTAG | 51455 |
| rs559211105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423476 | TGACAGAAACTTTAT[C/T]TGGCTCCCTTCAGAA | 51455 |
| rs559224775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404862 | TCTTGGCCTTTTGTC[A/T]TTGAAGCCTGAAGTA | 51455 |
| rs559224842 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483071 | TAAGATATTGAAGAA[G/T]AAATTGTTAAAACAT | 51455 |
| rs559248570 | snp | A/C | 0.0003999 | 0.0141347 | intron-variant | REV1 | GRCh38.p7 | 2:99435978 | TCAAACCCCAAGCTA[A/C]TTTTTACTATTTAAA | 51455 |
| rs559254440 | snp | A/C | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490873 | GTAAGTACAATTCTA[A/C]TTGAGGGCCTTCTAG | 51455 |
| rs559285350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444067 | CCTCGTGATCCACCC[A/G]CCTCTGCCTCCCAAA | 51455 |
| rs559291082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474813 | GGACTGAGGCACGAC[A/C]ATCACTTGAACGCGG | 51455 |
| rs559308233 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99479275 | GAGGCTGCAGTCAGC[C/T]GAGATTAGGCTACTG | 51455 |
| rs559501606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489186 | ACGGCGCCCAGCGTA[G/T]TTAGCGAACGGACAA | 51455 |
| rs559630521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421337 | ATCAACCATTTACTT[A/G]TATTTCCAGCACTTA | 51455 |
| rs559635959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99488825 | GTGCCAAGTCCGGAA[A/T]GACCAGACAGATACA | 51455 |
| rs559665675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99438446 | TATTTTAATAAATTA[G/T]CTTTCTATGTTATGC | 51455 |
| rs559702238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99446129 | ATTTAAGATATATGC[C/T]AACACTGATCCATTT | 51455 |
| rs559723170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451182 | TGGGCACCAAATCCA[A/G]TGAAATCACAGAAAT | 51455 |
| rs559736063 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490734 | GTCCTTTGAGTGCCC[C/G]GGCAGCATTGCGCCT | 51455 |
| rs559808080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412518 | ATAATCTTTTAGTAT[A/G]TTTCCCCAAGAGCTA | 51455 |
| rs559837118 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416107 | AACATTTATGGGTAC[A/G]AGGGACTAAAGAGGT | 51455 |
| rs559849126 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99467384 | TGAAAATTTTAGCTT[C/T]GTCATTTCCAATAAC | 51455 |
| rs559933057 | in-del | -/ATC | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400138 | CCTAGGACAAGAATT[-/ATC]ATCTTACAAACTAAA | 51455 |
| rs559941544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476527 | CGCCATTGCACTCCA[A/G]GCTGGGTGACAGAGC | 51455 |
| rs559978354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484260 | GAAACGAGCAGAAAA[A/C]GTAACTATTGTGTAT | 51455 |
| rs559980162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475907 | AGAACTGCTTGAACC[G/T]AAGAGGCGGAGGTTG | 51455 |
| rs559995026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413481 | ATGCTATCACACATA[C/G]CACTGACCTGAAGAT | 51455 |
| rs560026820 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472316 | TCACAAAAAGACAAA[C/T]ACTGTATGATTCTAC | 51455 |
| rs560027919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483695 | TAATTTTACAAGAAC[A/G]TATCGTTTTATTTTC | 51455 |
| rs560063068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414619 | CACAGCTATTTGCTT[G/T]TAAGAAAGACTTTTT | 51455 |
| rs560100226 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468754 | TTAAAAAACGGATGA[A/G]GAGTGAATACATGAA | 51455 |
| rs560116634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468974 | GATAACAGTAGACTA[G/T]ATACGGACTCAAATC | 51455 |
| rs560151346 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428848 | TACAAAAAAATTAGC[C/T]GGGTGTGGTGGCGAG | 51455 |
| rs560169060 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99447494 | GACTTTCTAGAGATA[A/G]TAATGTACTTTTGAA | 51455 |
| rs560170735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455490 | AAGAAAAGTTTCAAA[C/T]GCTTAGGGAACAAAT | 51455 |
| rs560192408 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99453676 | AAGGCAGGCGGATCA[C/G]AAGGTCAGGAGTTCG | 51455 |
| rs560207691 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99454878 | CAGTAAAAGTAAAAG[A/C]CATATACAAGGACCA | 51455 |
| rs560283976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469725 | TTTCCTAATGTTTTA[C/T]CTTTTGCTGGAACAC | 51455 |
| rs560411582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432875 | TATAGTAAGATTGTA[A/G]CAGAAGAAAAGACAA | 51455 |
| rs560437156 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99401848 | GCAATCATGGTTCAC[C/T]GCAGCCTCCACCTCC | 51455 |
| rs560453441 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99407357 | GGAGTTTGAAACCAG[C/T]CTGGCCAACATGGTG | 51455 |
| rs560463125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99430794 | TTGAGAAATAAATTA[A/G]AACACAACTTCATCA | 51455 |
| rs560500168 | snp | A/G | | | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421547 | CTTTGATTTCCATAC[A/G]AACAGCATTTGCAAA | 51455 |
| rs560511157 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99407562 | TCTCAAAAAAAAAAA[A/C]CCCCACACAAAAATC | 51455 |
| rs560536239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464055 | GGAAAGAATACAATG[A/G]ATGCTCCAGTGGCTA | 51455 |
| rs560545121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478643 | TAACAGGAAGAACAG[A/T]ACTTAGCTGAAGAAT | 51455 |
| rs560653312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484423 | AGCAGGAAACACATC[A/G]CTAGTAACTTTTACT | 51455 |
| rs560699148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454192 | GCCATGAGTTTGAGA[A/C]CAACCTAGGCAACAC | 51455 |
| rs560704201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431837 | GACACACTGTCCTCA[C/T]TGGAGGGCAAAGTAG | 51455 |
| rs560716989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485007 | CACAGTAAATAATAA[A/C]TCACAATTATTAAAT | 51455 |
| rs560808418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447947 | GGTCTCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 51455 |
| rs560824201 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440318 | GCATTAATTCAATTA[C/G]AGCGCAGGCTCCAGA | 51455 |
| rs560846485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461950 | ATGACAATAGGCACA[C/G]CTGGTGGGGAGGAGG | 51455 |
| rs560857560 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99490111 | CGCGCTCACAGCCGC[A/G]CGGCGCACGCGCTCT | 51455 |
| rs560870501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421737 | ATAGTCTTCTTATCC[C/T]CTCTTTTTTCTATTT | 51455 |
| rs560883428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461253 | TCTTACTAAACCAGA[C/T]AAATGTACCAGTTAA | 51455 |
| rs560903172 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476294 | TGGGAGCAGTGACTC[A/T]CGCCTGTAATCCCAA | 51455 |
| rs560909696 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466329 | CTCACAACCACCTCC[A/G]CCTCCCGGGTTCAAG | 51455 |
| rs560992382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482693 | ACGTTGTGTTTGCTT[C/T]GGCTGCACATACACT | 51455 |
| rs561016501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99414444 | AATACCAAAGACCCC[A/G]AGTTAACAATTTAAA | 51455 |
| rs561051117 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456287 | GTTCTAGGCACTGGA[A/G]ATATGGCAATGAACA | 51455 |
| rs561056850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468396 | ACTACTTGACAGAAA[C/T]ATCCTTCAGAAATAA | 51455 |
| rs561072214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431028 | CAGCATTTCTCTTTT[C/G]TTTATTTCAGACTCA | 51455 |
| rs561073259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99438065 | CAGAAAAACAGTATG[C/T]TACTGTGTGTGCATT | 51455 |
| rs561073577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429314 | CACTATAAGATAAAG[A/T]CCTATACAAAAAGTT | 51455 |
| rs561104660 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99414454 | ACCCCGAGTTAACAA[C/T]TTAAAAAAAAAAAAA | 51455 |
| rs561104707 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99449259 | GACAAAGCGAGACCC[A/T]ATCTCAAAAAAATAA | 51455 |
| rs561116417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478566 | AAGCCAAATGATTAT[C/T]TGTAGAAAAGTTCAA | 51455 |
| rs561129652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475788 | AGGAGTTCAAGACCA[C/G]CCTGGTCAACATGGT | 51455 |
| rs561189896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99476683 | AGCCATGTATTATCA[A/G]CCTCCTGAAGGGCTG | 51455 |
| rs561216071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99437463 | AACTCCAAAGCCAGA[C/T]ACTTCCTTACTACCC | 51455 |
| rs561233948 | snp | C/T | 1.67534e-05 | 0.0028942 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401210 | CACTTATGGCACAGC[C/T]ATCAGAGAGCATCAG | 51455 |
| rs561248039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408213 | TGGAACTGTTTAAAA[A/G]AGTTATAGAAAAGTT | 51455 |
| rs561259820 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99408181 | TTCCATATGTATTCA[C/G]TAGTACTAAAGTAGT | 51455 |
| rs561328647 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99470441 | AACTTCTCTTAGAAG[C/G]AAAATTTATTCAAAG | 51455 |
| rs561358066 | in-del | -/GAT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400770 | TGGAGACAAGAATAA[-/GAT]GATGGTTTAGAAGCT | 51455 |
| rs561363268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477494 | ACAGGAGAAAGAAAA[A/T]CTTAAAAATTGTTTG | 51455 |
| rs561385235 | in-del | -/AAAT | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99485326 | GTATCTGCTAAAGAA[-/AAAT]AAATCATTATGAAAA | 51455 |
| rs561405651 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99473019 | TACAGACATGCACAT[A/C]CCACAAACTAGTCAG | 51455 |
| rs561486078 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99457308 | GTAAAGATGTCAATT[C/G]TCCCCGAACTGATCT | 51455 |
| rs561497604 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99485105 | AGGATCCTATTACTT[C/G]TTAAAGTTCAGACTG | 51455 |
| rs561502626 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99429575 | TTCACTCTTCAAAAG[A/G]CAGTAAAAACGATGA | 51455 |
| rs561530995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99449243 | GCACTCTAGCCTGGG[C/T]GACAAAGCGAGACCC | 51455 |
| rs561605251 | snp | G/T | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99462798 | CAATAAATAAAACAG[G/T]AAAGTTGGGCCGGGC | 51455 |
| rs561625051 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99461934 | CCAGATACCGGACTC[-/A]ATGACAATAGGCACA | 51455 |
| rs561686160 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432255 | ACTAAGAAACTAAAG[C/T]TTCAAAAAGGACTAA | 51455 |
| rs561696932 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99409926 | TTACAGTGATTCATT[C/T]ATCTTTTTACCAATT | 51455 |
| rs561781946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404313 | AGCCCACTCTCCCCT[C/T]CCCTCCCCTCCCCTC | 51455 |
| rs561809688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417093 | TGTCTTCCCCAAATT[A/T]ATATGCTGAAGTCCT | 51455 |
| rs561861122 | in-del | -/AAA | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99408736 | CTTCAGAGCCTTTTG[-/AAA]AGCTTCTCTGGCATG | 51455 |
| rs561866704 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432820 | TGACTAAACTGATGA[A/G]GACAAGTAACCAATG | 51455 |
| rs561940552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99409305 | TCTCTGTTTAAGAGC[A/T]GTCGTCTCACGACTT | 51455 |
| rs561999382 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99488621 | AAGTGTCCAGTACAG[A/G]AAGGCAGGGAACAAT | 51455 |
| rs562010461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487690 | TATACTCTATGATTA[C/G]TAATACGCCACATAT | 51455 |
| rs562037760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458946 | GGGCGCGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 51455 |
| rs562053760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419152 | TCTCTTTGCTCTAAC[A/G]CAAGTGCCACTTCAG | 51455 |
| rs562054289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416336 | CCACCACAGAAGGTT[C/G]CCTCTCCTATATGAA | 51455 |
| rs562130798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472520 | ATGGTAAACTTTTAT[A/G]TGTATCGTACCACAA | 51455 |
| rs562131709 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99466197 | ACCTCGTGATCCGCC[A/G]GCCTCTGCCTCCCAA | 51455 |
| rs562143600 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401099 | CAAATTTGGCACTTT[C/T]TGAAAAGAAATGTAC | 51455 |
| rs562241004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99427190 | TCATCTCTGGGGGAA[A/G]AAAATTGCCATCAAA | 51455 |
| rs562265427 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447001 | GAAGAGACACATACC[C/T]AAAAGCCATTTTAAT | 51455 |
| rs562299998 | in-del | -/A | 0.338069 | 0.233974 | intron-variant | REV1 | GRCh38.p7 | 2:99453355 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAG | 51455 |
| rs562309500 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99413832 | AAATTTTCCATCAAT[A/G]AGGAAAAGACAGCGT | 51455 |
| rs562326467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448612 | CATGCTAAAAACCTA[C/T]GTGATAGACAACATG | 51455 |
| rs562357765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434798 | AGTGGGGAAAGAAAA[A/C]CTAAATTTTTTTTTG | 51455 |
| rs562374580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470332 | TTTAATCAGTCTTTA[C/T]TAATACAGTCATATA | 51455 |
| rs562377607 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402765 | CTGCAAACTAGAAAG[C/G]CCTGGCACACCTGAA | 51455 |
| rs562379420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413846 | TGAGGAAAAGACAGC[A/G]TTGTGTTTCTGGTCT | 51455 |
| rs562393847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434213 | CATCCTTAAAACCCC[C/T]GAATGAAAAAGCTAA | 51455 |
| rs562411400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469797 | TACTATAGTTATTGG[G/T]AGATTTTACTATCTA | 51455 |
| rs562491753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448018 | AAGTTTCTAAAATTA[C/T]ACCAGGTTATATGGA | 51455 |
| rs562511927 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99410633 | GTTTTCTTCATTTTC[C/T]ATTACTTACAACAAC | 51455 |
| rs562566044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99455575 | AGGTGGCATAAATTA[A/G]TATGGTAAGTCTTCT | 51455 |
| rs562573715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462052 | CCTTCCCTGCTTGGC[A/G]ACCCAAATGCTGGCA | 51455 |
| rs562594713 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99401930 | TTTTGTATTTTTCAG[G/T]AGAGATGGGGTTATG | 51455 |
| rs562600221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99422358 | ACTAAGAAATCACAA[A/G]ATAGAACTGGACCAG | 51455 |
| rs562611419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477323 | AAGAAAGCTGTTTAC[C/T]TCTTTTTCTGGGATG | 51455 |
| rs562621668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | REV1 | GRCh38.p7 | 2:99424802 | TTGACCAATTCCATG[C/G]TCCTGAAGTGGCTCC | 51455 |
| rs562622876 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99411808 | TCCAACACTGTGCTT[-/A]ACAGCCCAAACATCA | 51455 |
| rs562640613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416266 | TAGTCTTTAACAAAG[A/T]TAAATAGGTTTCTTT | 51455 |
| rs562684488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417414 | CTCCCACAGTGCTGG[G/T]ATTACAGGTGTGAGT | 51455 |
| rs562698191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462752 | ACCAGAACATAATGA[C/T]GACCTCATAAACATA | 51455 |
| rs562752560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99415556 | TGATGGAAATGTTCT[C/T]GTCTGCTATCCAATA | 51455 |
| rs562848934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99479199 | CAGGTGTGGTGGCAC[A/T]CCCCTGTAGTCCCAG | 51455 |
| rs562941238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471830 | TCATTAATCACTATG[C/G]AAATGCAAATAGAAA | 51455 |
| rs562954019 | snp | A/G | 0.000479811 | 0.0154814 | intron-variant | REV1 | GRCh38.p7 | 2:99435819 | TTTTCTTAAAACATA[A/G]GCAAGAATACAGACC | 51455 |
| rs562979789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471152 | AAACACAATTTGCCT[C/T]TGGTGCCCTGCCATA | 51455 |
| rs562984963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99486386 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGT | 51455 |
| rs563037788 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99449058 | AGGCCAAGGCTGGAG[G/T]ACTGTTTGAGTTTGA | 51455 |
| rs563052134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425909 | GAAGTGGTGGCGCAT[C/G]CCTGTAATCCCAGCT | 51455 |
| rs563075605 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99408272 | TGAATGCCATAGTCT[-/C]CCCTTCAAGGAAGCC | 51455 |
| rs563091275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435059 | TACTTAATGCATTAT[C/T]CTGAGGACCAAGAAA | 51455 |
| rs563106043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432973 | CTGCCGATAAAAGGA[C/T]GTGTGTAACAAGACT | 51455 |
| rs563233445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99404203 | CCCCAGATCAGTGTG[C/T]TTCTGTCTTAGCATG | 51455 |
| rs563245050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411137 | TACTAAAAATGCAAA[A/C]ATTAGCCTGGCGTGG | 51455 |
| rs563310536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427516 | TTTGCTGGCCCCATT[A/C]TTAAGCTATGTATAG | 51455 |
| rs563321004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99462240 | AAGTCCTACTACCCA[C/T]GTGTGGTAATTTCCC | 51455 |
| rs563378234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99488096 | ACCTCCATGTAACTG[C/T]GAACTTCCTGTCTTT | 51455 |
| rs563387920 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | REV1 | GRCh38.p7 | 2:99489267 | GTTCTGGGATGCACC[A/G]GGGACGTCGAAGGCG | 51455 |
| rs563502521 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99472629 | AGGATCTTCAGGTGG[A/G]GTGCAAAGCTGGGAA | 51455 |
| rs563532749 | snp | A/C/T | 0.000115312 | 0.00759245 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404487 | TTTATTCCTGCGTCA[A/C/T]TGTTCGATTCTTGAG | 51455 |
| rs563556159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458991 | AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 51455 |
| rs563589211 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99469978 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGTC | 51455 |
| rs563592401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99452310 | TGTGTGCCTGCAGTC[C/G]CAGCTACTAGGGAGT | 51455 |
| rs563593159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466432 | TTTTTAGTAGAGATG[C/G]GGTTTCACCATGTTG | 51455 |
| rs563685555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445270 | AGTTTTGACTCATAT[G/T]TAAGCACATGACAAA | 51455 |
| rs563744349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99443169 | TGGCTACTCTACCTT[C/T]AAAATTATCATTTCA | 51455 |
| rs563778965 | snp | A/G | 1.66488e-05 | 0.00288515 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405925 | CTGGGAAGGTGACGG[A/G]ACCTCTATACTCAGG | 51455 |
| rs563866858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419985 | AAAGGCACTGAGGAG[C/T]GGAAATATAAAGTGG | 51455 |
| rs563878226 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480401 | CCAGATGTAGAGGTA[C/G]ACAAACTAAGGTAGG | 51455 |
| rs563880792 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99450401 | ATGCTCTAACTCACA[A/C]CTCCCCTAACAACAG | 51455 |
| rs563972955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487775 | GACTTGTTCATTTAT[G/T]TGGAGACGAGAGGTA | 51455 |
| rs563977582 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99474020 | GCAGAAAATTGGAAA[A/C]TACAGAAAACAGAAA | 51455 |
| rs563978190 | in-del | -/TCTT | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400139 | CTAGGACAAGAATTA[-/TCTT]TCTTACAAACTAAAC | 51455 |
| rs564142756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457422 | TGCACTGGCTCACAC[C/T]TGTAATCCCAGCACT | 51455 |
| rs564185825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99464761 | AGTTTAGGGGATAAA[A/G]TTTATAAACATCATA | 51455 |
| rs564193112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486709 | GGGAGCCAGAGAATT[C/G]TGACCCTAGCTGTCT | 51455 |
| rs564374328 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99473271 | TACTCAGGAGGCTGA[C/G]GCAGGAGAGTCACTT | 51455 |
| rs564382996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458984 | GAGGCCAAGGTGGGC[A/G]GATCACGAGGTCAGG | 51455 |
| rs564419220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404910 | AGAAGTGTATATATA[C/T]TACCAGCCACTATCA | 51455 |
| rs564439088 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99425791 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 51455 |
| rs564493136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99451347 | ATAAAGTACTCACCC[A/G]TCTACTAGCTGCTCT | 51455 |
| rs564528139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459157 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 51455 |
| rs564531814 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99428923 | CATGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 51455 |
| rs564572825 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460480 | AAAATATATATATAG[A/G]CATTTTACAAAATAG | 51455 |
| rs564619811 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99459140 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 51455 |
| rs564620546 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421596 | GGTCTCTGCAAGGAT[C/T]TCGGTAATGTCTACC | 51455 |
| rs564642463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99411220 | TTGAACCCAGGAGAC[A/G]GAGGTTGCAGTGAGC | 51455 |
| rs564642491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419935 | TTCTGGGAAGTCACA[A/C]CAAAATGATAAAAGT | 51455 |
| rs564726477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99460145 | GCAGTGGCGCAATCT[C/T]GGCTCACTTCAACCT | 51455 |
| rs564738598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465894 | CACCTTAAACCATGA[C/G]ACTTTACCCCACACA | 51455 |
| rs564758373 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443681 | ACATACTATACTAGT[C/T]GCAAGACATGTAACC | 51455 |
| rs564833894 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | REV1 | GRCh38.p7 | 2:99477217 | TACATTTCCCACGCT[A/C]CTCTCAAAATCGGGG | 51455 |
| rs564873291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468892 | TACACACGTGGAAAC[C/T]CTTTGAAAACTATAA | 51455 |
| rs564938975 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99436999 | TTTTTTGTTTTTTTT[G/T]TTTTTTTGAGATAGG | 51455 |
| rs564948062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99474829 | ATCACTTGAACGCGG[C/T]AGGCAGAGGTTGCAA | 51455 |
| rs565001534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482474 | ATAACCTGCAAGTCC[C/T]GGAGTTTGTAGCTAA | 51455 |
| rs565023654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429234 | TATGAGGAAGATATA[C/T]ATATATGAGTGTGTG | 51455 |
| rs565059304 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483516 | TTTTAATTCAAGCAC[-/A]AAGCCATGGGACCCG | 51455 |
| rs565083359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447265 | GCAACCTCTGCCTCC[C/T]AGGTTCAAGCGATTC | 51455 |
| rs565119764 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99446525 | TTTTTGAGACAGTCT[C/T]GCTCTACCACCCAGG | 51455 |
| rs565127683 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99489962 | CTGAGCAGCGCCGCG[A/G]TCCACGCTCCCCCAC | 51455 |
| rs565135602 | in-del | -/TGTT | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99473639 | TTTTGCCACTTTATG[-/TGTT]TTTTTTACACCTTCA | 51455 |
| rs565143481 | snp | A/T | 9.34361e-05 | 0.00683442 | intron-variant | REV1 | GRCh38.p7 | 2:99429968 | AAAAATAAAAAAAAA[A/T]TAATGGTTATATGTT | 51455 |
| rs565183404 | in-del | -/TCTTTAAAG | | | intron-variant | REV1 | GRCh38.p7 | 2:99413056 | ACTAGTTTAAAATAA[-/TCTTTAAAG]TCTTTAGGCAACATA | 51455 |
| rs565223347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444614 | AATCAGATATCCTCA[A/G]AGATACTCAATAAAA | 51455 |
| rs565231457 | in-del | -/A/AA | 0.262985 | 0.249663 | intron-variant | REV1 | GRCh38.p7 | 2:99475686 | GCAACACTCTGTCTC[-/A/AA]AAAAAAAAAATAAAT | 51455 |
| rs565243866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414380 | GCGTTAAGCGTGCTC[A/G]TTCACAATTGTGCCA | 51455 |
| rs565252976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99430881 | AATCACATTCTAAAA[C/T]CACAACCTCAGCCAC | 51455 |
| rs565253237 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490898 | TTCTAGCAGAAAACA[A/C]TCCGTCCATAAGGAC | 51455 |
| rs565286792 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99426581 | AACCTTTTTCCTTTG[A/G]TTTGCCTTAGGTTTG | 51455 |
| rs565326011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484279 | ACTATTGTGTATCAG[G/T]CTTAATACCTGAGTG | 51455 |
| rs565366100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458710 | CTGAACAATAAAAAG[A/G]CAACAATTTTGATGA | 51455 |
| rs565396324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453611 | AATAAAAAATCAAAA[C/T]AGGCCAGGTATGGCG | 51455 |
| rs565448330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99406780 | GAATACTGTATTCCA[C/T]TGATGTTCTCGTCAA | 51455 |
| rs565498083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427582 | TCCCCACAATCTAGT[A/C]CCCACTCCAAACTCA | 51455 |
| rs565534902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461144 | GTGAACTTCCCAATG[C/T]TGCACCAGCATTTAT | 51455 |
| rs565560071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99427046 | AAATTAGCCAGGCGT[A/G]GTGGCGGGAGCAGTA | 51455 |
| rs565569544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407484 | TTGAACCCAGGAGGC[A/G]GAAGTTGCAGTGAGC | 51455 |
| rs565603606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466083 | AGTAGCTGGGACTAC[A/G]GGTGCCCGCCACCAC | 51455 |
| rs565615582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456182 | ATCTGAGTGAAAATA[C/T]TTTAACATTCTGATG | 51455 |
| rs565625667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411580 | TCTGGCTAATTTTTT[C/T]GTATTTTTAGTAGAG | 51455 |
| rs565639769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472808 | GCATGCCCTAAAAAA[A/T]GTTTGGTAACAGTCT | 51455 |
| rs565644327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99412060 | AACACGGTGAAACCA[C/T]GTCTCTACTAAAAGT | 51455 |
| rs565655667 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99429753 | GTAACATTTAAATCC[A/G]CTTCAAAAGATTATA | 51455 |
| rs565678468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434503 | GGAATGTTAACAACA[G/T]GTAAGCAAAAATTTT | 51455 |
| rs565685961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419457 | CCTCATGATCCACCC[A/G]CCTCAGCCTCCCAAA | 51455 |
| rs565697158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99466543 | CACCATGCCTGGCCA[A/G]CAGATATTTTCTTAT | 51455 |
| rs565745686 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99485659 | AGCATCTTCTACAGA[A/T]TGAAAAATAAAAAAC | 51455 |
| rs565786566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474602 | CTAGACCCCAACTAG[A/T]CCATATTGATAAGCA | 51455 |
| rs565950931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99452523 | ACACTGCCTACAGAA[A/C]CCATCTCTGCAATGT | 51455 |
| rs565955824 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99488239 | TGCTCTTATGTAGAA[A/T]CAGAGTTTTGAAGTT | 51455 |
| rs565987398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451673 | AGTCTGGCATGTAGA[A/G]GTCACTCAATATGAA | 51455 |
| rs566004538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487003 | TATAAAGGAAGGGGC[C/T]GGTTCCTATTTTAGA | 51455 |
| rs566004768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443467 | GAAATGACTGAATTG[C/G]CTTACAGAATACTAA | 51455 |
| rs566038315 | snp | C/T | 0 | 0 | intron-variant | REV1 | GRCh38.p7 | 2:99421074 | CAGTTACTGAGAGCA[C/T]TTGGAGTCAGGGTGA | 51455 |
| rs566094023 | in-del | -/AA | 0.0244538 | 0.107838 | intron-variant | REV1 | GRCh38.p7 | 2:99487638 | TGGTGCTATTATAGT[-/AA]AAAAAAAAACTTTTC | 51455 |
| rs566099674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428884 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51455 |
| rs566137343 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470534 | CTTAGCTCCCACAAT[G/T]TAGCCTAAATATTTG | 51455 |
| rs566205454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437136 | AGGTGCGTGCCACCA[C/T]GCCCAGCTAATTTTT | 51455 |
| rs566228991 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400647 | ACATAATGTTCCCAG[A/G]AAAAAAATCTTCAAG | 51455 |
| rs566245526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99444780 | ACAGAAACATTATCT[A/G]AAAGCATATTTGTAT | 51455 |
| rs566301859 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99434986 | TTCCTTTTGTATGCA[C/T]GTTAAGTTACAAGAT | 51455 |
| rs566338647 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463318 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGACCA | 51455 |
| rs566387290 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99405261 | CCCTTTGGAAACATG[A/C]AATCCCATCAACTGG | 51455 |
| rs566456148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99407722 | TACAAAATTTATGTA[C/T]TCATATTCCTCACAG | 51455 |
| rs566491351 | in-del | -/CAAAGA | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99424693 | CCAGGGTTCATCCCC[-/CAAAGA]CAAAGAATATAAACA | 51455 |
| rs566492271 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99446788 | ATGAGCTATCGCACC[A/C/T]GGCCGGAAAACACCA | 51455 |
| rs566523916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99455914 | TGCTTTTTCACAAAC[G/T]TCAGCAGTGCCAAAA | 51455 |
| rs566526445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454313 | CCAGCACTTTGGTAG[A/G]CCACAGCGGGTGGAT | 51455 |
| rs566539869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461418 | AGAATTCTAAGATGC[A/G]GATTCATTCAGGGAG | 51455 |
| rs566599733 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400407 | GTAATCTGTAGCTAG[A/T]TTTAGGGTTTTGCTG | 51455 |
| rs566610257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416609 | AGCTTGGCCAGGACA[C/T]GTAACTTCACACTTG | 51455 |
| rs566626756 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99450998 | AAGGTTAAGTTAAAA[A/C]CTGAACTACAGCATC | 51455 |
| rs566663692 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99467873 | CAACATGGTGAAATC[C/G]CATGTCTATTAAAAA | 51455 |
| rs566668530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99453775 | ACACGCGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 51455 |
| rs566681280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424341 | CAACTCAAATATTTA[C/T]CAAATATGTTGATAT | 51455 |
| rs566700319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476269 | CTAAGCCCTTAGAAC[A/G]TCCACCTTATGGGAG | 51455 |
| rs566722465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99409565 | ACGAGTGTTTCAGAC[C/T]GGGCACATTGGCTCA | 51455 |
| rs566731903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99468606 | CCCAATTTAATTCCA[C/T]ATAACTTGATGACCT | 51455 |
| rs566788304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463122 | TAAATATAAATACAT[A/G]AAACACATAGGTCAA | 51455 |
| rs566819827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421944 | ACAAAAACACAGCAT[A/C]AATTATTATTTCAGT | 51455 |
| rs566828790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401648 | GCTACCCGGGAGGCT[C/G]AGGCAGGAGAGTCAC | 51455 |
| rs566874760 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99479255 | CTGCTTGAACCAGGG[A/G]GTCAGAGGCTGCAGT | 51455 |
| rs566915734 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482683 | AAGATATAAAACGTT[A/G]TGTTTGCTTCGGCTG | 51455 |
| rs566940558 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99408616 | CATTGTGTTTACAGT[A/C]CAGCCAATAAACAAT | 51455 |
| rs566946687 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462814 | AAAGTTGGGCCGGGC[A/G]CAGTGGCTCACACCT | 51455 |
| rs566988998 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418003 | TTAAGTTATATACTA[C/T]GGGGGTCAGGAAGCT | 51455 |
| rs566999878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99406897 | ACTTCTCAAAAAATA[C/T]TGGCGGGAGTGATGA | 51455 |
| rs567061749 | snp | A/G | 0.00128765 | 0.025341 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406102 | ATCCACAGCAGCCCG[A/G]AATACTACAAAAAGA | 51455 |
| rs567138862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412117 | GGGTGCCTGTAATCC[C/T]AGCTACTTGGGAGGC | 51455 |
| rs567164309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445011 | AACTATATTCTGATA[C/T]ATACATGAAAGAGTT | 51455 |
| rs567193933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484061 | ATGTGTTCCTCCTTA[C/T]TGAAGGAGATCCAGG | 51455 |
| rs567228802 | in-del | -/AACTAAACTATCA/AACTAACTAAACT | 0.0433807 | 0.14092 | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400146 | AAGAATTATCTTACA[-/AACTAAACTATCA/AACTAACTAAACT]AACTAAACTATCATC | 51455 |
| rs567231455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99445526 | ATCTGTAGCAACTTA[A/G]GACAATATTTTTAAA | 51455 |
| rs567347648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461712 | GACTTTACAGTTCAG[C/T]GAAAGATAAAACTGA | 51455 |
| rs567461394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459652 | TTGAAGCTGCAGTGA[C/G]CCGTGATAGTGCCAC | 51455 |
| rs567468341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99420954 | GAGTTCCAGAGGACA[C/T]GGCTGGAAGAATCAA | 51455 |
| rs567483877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99430159 | GCAGATAAAAACTTA[C/T]AATAAATTCAAAGTG | 51455 |
| rs567500591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467694 | ACAAGAAATTGGAAG[G/T]AGACAGACCAAACTT | 51455 |
| rs567520593 | snp | A/C/T | 0.000379137 | 0.0137633 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438823 | CTGCCTTGCTAAACG[A/C/T]AGATACTGAAGAAGT | 51455 |
| rs567544647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99430730 | CTCTGGAGAGCCTAC[C/T]GGCTGCATGCCACTT | 51455 |
| rs567547381 | snp | A/G/T | 0.00239401 | 0.0345304 | intron-variant | REV1 | GRCh38.p7 | 2:99411956 | AAGACATATCCAGCC[A/G/T]GGCGCAGTGGCTCAC | 51455 |
| rs567554902 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482078 | ACCATGTGAATAGTG[C/G]GTTGGGCTTTGAGCA | 51455 |
| rs567583868 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469893 | CTGGGGGGCCGAGGC[A/C/G]GGCAGATCACGAGGT | 51455 |
| rs567594274 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99468073 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG | 51455 |
| rs567605421 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490398 | TCGGTTGCCATTCGG[A/G]CAGCGCGCCGCTCCG | 51455 |
| rs567635612 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99444447 | CTACAGGTACTCTCT[A/C]TGGTCAGCACTGATC | 51455 |
| rs567637260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407831 | TACAGTAAGAATCTA[A/C]GAAAATTATTCTAAA | 51455 |
| rs567657439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437734 | ATTAAATAACCTTCA[A/G]GTAACAAGGCCAAGA | 51455 |
| rs567688987 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99455221 | GCTTATACCTCCTTT[C/G]CTCCTACCATGGCAA | 51455 |
| rs567714573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469300 | AAGACTGATAACTAA[A/G]AGTAATGAACTAAAA | 51455 |
| rs567719327 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99427153 | CACCACTGCACTCCA[A/G]CCTGGGCAAAAGAGC | 51455 |
| rs567780682 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99421127 | GGAATAGCTCCATGT[A/G]CCGGGAGGCTGAAGT | 51455 |
| rs567791212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485193 | ATAACTGGTATTATG[C/T]AAGTTCAATTACCAC | 51455 |
| rs567797625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423160 | TTTTCTCTCTCTCTC[C/T]TACTAAAGCAAGCTC | 51455 |
| rs567809525 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99477743 | GAAAGCGTCTATCCC[A/C]AACAATTCAATACAA | 51455 |
| rs567827752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484625 | TTAATTACGATGCAA[A/G]TCATCATCCTATTAA | 51455 |
| rs567936784 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483087 | AAATTGTTAAAACAT[C/T]TGTAAAGTTCAGAAC | 51455 |
| rs567938715 | in-del | -/CTAA | 0.00676609 | 0.0577691 | intron-variant | REV1 | GRCh38.p7 | 2:99446893 | CATTCCCTCCAAAGC[-/CTAA]CTATTGCCCCCAGAT | 51455 |
| rs567944987 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491017 | CTTTTTTCCCACTCA[G/T]TCCCTTGCCTAAAAT | 51455 |
| rs567959912 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426256 | GGAGGCTGAGGCAGG[A/T]GAATCGCTTGAACCT | 51455 |
| rs567964360 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99455037 | TTGCTCATCTGGTTA[A/C]AACAAATTCTATAAA | 51455 |
| rs568022685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433101 | AATATATGACAAGTA[C/T]TGTGTACTTCCTTAA | 51455 |
| rs568064539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432288 | ATGCTATTTGTCCTA[A/C]TACTTTGTCTAGACA | 51455 |
| rs568103565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440644 | CCTAATTTGTCACAT[A/G]CAGAGAAAGTTCAGC | 51455 |
| rs568137758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448044 | ATGGATACTGAACTG[C/T]CGAGTTTGGAAGTTC | 51455 |
| rs568246918 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99423049 | AAAGTTAATTAGTGT[A/G]TTCTCTTTGTGTTAA | 51455 |
| rs568260396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447673 | GGCAGATATTAGCCT[C/T]CTTTCACAAATGAGG | 51455 |
| rs568403306 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99408394 | AGGTCAACTAAAAAT[A/C]AGTTGAGAAATTTAG | 51455 |
| rs568523497 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99457528 | CTCTACTAAAAACAC[A/C]CAAAAAATGAGCTGG | 51455 |
| rs568568486 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491587 | ACCGTGCCTGCCCAT[A/G]ATTTTAACAGACTCA | 51455 |
| rs568593903 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491795 | TTCAAACCGAAGATC[A/T]TTTTTTTTCTTCTTT | 51455 |
| rs568623319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471242 | CTGCTAAGGCATTTA[C/T]TGACAACTAAGGAAC | 51455 |
| rs568623692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99430915 | TCTACTATTATAAAC[A/G]AAAGTACCATGAGTA | 51455 |
| rs568632371 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491272 | TTTAAAACAAATTGC[A/G]TAATTGCTTTCTTTT | 51455 |
| rs568640459 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462619 | TGGCAGCCATATACC[C/T]ACCCTAGAATTAAAG | 51455 |
| rs568646116 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99417625 | CCTACAAGCCAAGCA[A/G]AGGCTTCAGAAAGAG | 51455 |
| rs568662711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456963 | TTGAAAATGTAGGTC[A/T]GAATTAGGACTAGAA | 51455 |
| rs568819335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469226 | TTTTTTCCCCCGTAA[A/G]TTTTAGGTTTAGGGT | 51455 |
| rs568863661 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99401565 | CAGCCTGGCCAACAT[C/G]GTAAAACCCCGTCTC | 51455 |
| rs568877351 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484428 | GAAACACATCACTAG[G/T]AACTTTTACTAAATA | 51455 |
| rs568916910 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99425037 | ATCACTCTGTAAAGA[-/G]ATCAAGAAAAAAAAT | 51455 |
| rs568932206 | snp | G/T | 1.65102e-05 | 0.00287312 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439100 | CACCAAGCAATCCTG[G/T]GTCTTTAAGGCACCA | 51455 |
| rs568956537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99454894 | CATATACAAGGACCA[C/T]AATTTAGCCCACGTT | 51455 |
| rs568978072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443976 | GGCGCCTGCCACCAC[A/G]CCCGGCTAATTTTTT | 51455 |
| rs569029110 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99435053 | TATATTTACTTAATG[C/T]ATTATTCTGAGGACC | 51455 |
| rs569033790 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99408833 | TCTTTCCAAAGGAAA[C/G]TTATTTCGTGTTTTG | 51455 |
| rs569044756 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99473888 | TATTATTCCTTCATC[A/G]CTGACTTGTGTTTAT | 51455 |
| rs569047723 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99409619 | GAGGCTGCGGTGGGC[A/G]GATCATTTGAAGTCA | 51455 |
| rs569061298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99416784 | CCGGCTGTGTGGTGG[A/G]TGCCTGTAGTCCCAG | 51455 |
| rs569070077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99446880 | CACAGAAATTCCCCA[A/T]TCCCTCCAAAGCCTA | 51455 |
| rs569105010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461538 | GATAGCAGGTATCAG[C/T]CAGCTGAGAAGGGGA | 51455 |
| rs569126127 | snp | C/T | 1.84398e-05 | 0.00303637 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403058 | TTCTTCTTGTTTCTT[C/T]TCTTTTCTTTCACTG | 51455 |
| rs569192958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456715 | ATGCTATGAATTATA[C/T]ATCTCTCTATATAAA | 51455 |
| rs569214752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414849 | CCTGGGTTGTGTTAG[C/T]GTGTCCATGTGTTGG | 51455 |
| rs569218535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99407250 | ATGCACCACCACACC[C/T]GGCTAATTTTTGTAT | 51455 |
| rs569306697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456023 | CAATCTCACACCACT[A/G]AAGTGCAACCACTGT | 51455 |
| rs569340114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465273 | CCTAACATTCACTTA[C/T]ATAAAACACCAAATC | 51455 |
| rs569417491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478069 | AAAATCCCATCTTTA[A/T]AAAAATACAAAAATT | 51455 |
| rs569456360 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99485054 | CACAAAGCAGCAGCC[C/G]TTTGACTTTTAAAAA | 51455 |
| rs569496798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99431982 | AATCTATGACTAATA[C/T]GATTTTTAAAACTGT | 51455 |
| rs569501838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470581 | CTGGTCCAAGCAAGC[A/G]TTAGGTCATAGCCTG | 51455 |
| rs569538976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433544 | TTGTGACAAGCCCAA[C/T]GTTTTATAACTGACA | 51455 |
| rs569562049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99424371 | TCTCCCCATGCCACT[A/C]ATTTATAATTTCCAC | 51455 |
| rs569564860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418627 | GAAGCAAAACAAAAA[C/T]GTAACATTAAGGTCC | 51455 |
| rs569576034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99441634 | CATTGTCTTTCTATG[C/G]ATGGAACACAACAAA | 51455 |
| rs569622790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457722 | AGAGAGGCGTAGGTC[C/T]TAGAATAGCCAGAAT | 51455 |
| rs569622818 | in-del | -/AGAGCAAGAATAAGGAATTA | 0.0162398 | 0.0886349 | intron-variant | REV1 | GRCh38.p7 | 2:99403980 | ATCTTCAAAATGGTT[-/AGAGCAAGAATAAGGAATTA]AGAGCAAGAATAAGG | 51455 |
| rs569629355 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99415040 | TCCATGCAGGCTCAT[-/C]TGATGGAATGAAATG | 51455 |
| rs569655066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99479495 | AATGAGAATAAACCA[C/G]AATCCAAGGTTATCA | 51455 |
| rs569677469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99426912 | TTGCTGGCCGGGTGC[A/G]GTGGCTCACTCCTGT | 51455 |
| rs569793003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486897 | AGCAAACAAGTCTAA[C/G]GGGGGAAATAAATAA | 51455 |
| rs569799619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489032 | GAGTACATTAAGGAG[C/T]GTTATGTGAGATTAT | 51455 |
| rs569820831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99426321 | CATTGCACCTCAGCC[C/T]GGGCAACAAGAGCGA | 51455 |
| rs569830335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99488564 | AGAGAGCCTTGTATA[C/G]TGGAGAATGATTCCT | 51455 |
| rs569873712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99478944 | CGAGAAAGGTTATAT[A/G]CAGTAGAGAGAATGA | 51455 |
| rs569911331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486072 | TGAGGCTGCAGTGAG[A/C]CGTGATCACACCACT | 51455 |
| rs569993249 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481503 | GGTTACTATCACTAC[G/T]ACTAGTTTTAGCTGT | 51455 |
| rs570002333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99467553 | TGAGAACATTTGGCA[A/G]TCCTAGAAGAGTGGC | 51455 |
| rs570158885 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434809 | AAAAACTAAATTTTT[C/T]TTTGTATTTCTAGAG | 51455 |
| rs570169140 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99450889 | AACACATGTTACTAG[C/G]AGCTACCAAACTGGG | 51455 |
| rs570200942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435309 | AACCCAGAATGTATG[C/G]TTTTTAAAATACTGA | 51455 |
| rs570206036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458501 | GTATAAAATACTACA[A/G]CCACTTTGGGTAACA | 51455 |
| rs570236470 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99478227 | CTGAGACTCTGTCTC[-/A]AAAAAAATAAAAAAT | 51455 |
| rs570239041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99443618 | ATTCTACCTAAAGTA[A/C]CTTAACCTATATCAA | 51455 |
| rs570330134 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99476432 | ATGGTGGCACACGCC[A/G]GTAATCCCAGCTACT | 51455 |
| rs570333537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448884 | ACTTTTATTAGGATG[C/T]CAAATCCTAGGCTAT | 51455 |
| rs570371722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99448145 | GGCTAAATACACTAT[A/G]CAAAGGAACTGAGTT | 51455 |
| rs570400371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404072 | ACCTGGGCAAAATGC[A/T]CTAGTAGAAAATGGG | 51455 |
| rs570400453 | in-del | -/CTT | | | intron-variant, upstream-variant-2KB, cds-indel | REV1 | GRCh38.p7 | 2:99481431 | CAACAGAAGGCAATC[-/CTT]CTATCCATATTCAAA | 51455 |
| rs570418626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99426807 | AAAACAGCTTATTCC[C/T]ACATTTAAAGCACAG | 51455 |
| rs570602444 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418698 | ATTTTGTTTTTCATG[G/T]CACTCAATAAGACTT | 51455 |
| rs570608056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432381 | TCTAATTCCTAAACC[A/G]ATCCTCAATATTTTT | 51455 |
| rs570662725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99402126 | CAAAATAAAGGATAT[C/G]ACTTTCTCATTAACC | 51455 |
| rs570665359 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99454521 | CGCCATTGCACTCCA[C/G]CCTGGGCAACAAGAG | 51455 |
| rs570714798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99488275 | TGGGAAGTTGGAAAT[A/G]TAGTGATCTTATATA | 51455 |
| rs570821559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99471915 | AAAAAAAAAAAACAA[A/G]TGTTGATAAGGATAG | 51455 |
| rs570915996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450838 | TTTTACATTTACAAC[A/G]CATCTCAATTTAGAA | 51455 |
| rs570916361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99442679 | GAGCTGAACTAGTCA[A/G]TATTTTAAACCTCAT | 51455 |
| rs570931666 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458936 | TGTGGAGGCCGGGCG[C/T]GGTGGCTCACACCTG | 51455 |
| rs570932158 | snp | A/G | 0.000115612 | 0.00760214 | intron-variant | REV1 | GRCh38.p7 | 2:99404398 | AGTTGGAGCAGGGGG[A/G]TGAGAATATTGAAAC | 51455 |
| rs570947566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451772 | CTGCCCTAGACTCTA[C/T]GAAAAAAAAAATGAC | 51455 |
| rs570973698 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99409135 | GTTTTTAAAGTAAAT[-/A]AATAAATGACCACTA | 51455 |
| rs570988831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457641 | GGTAAGCTGAGATCA[C/T]ACCACTGTACTCCAG | 51455 |
| rs570990079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412657 | ATTGAGGGTCTAATG[A/G]TTTAGTTGTAGAGGT | 51455 |
| rs571019911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458334 | TAAGAAATAAACACA[C/T]GAAAGAATGTTCAAC | 51455 |
| rs571031761 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | REV1 | GRCh38.p7 | 2:99465170 | AGTGAAATTTGTCTA[A/T]AAAACACCCTCCTAC | 51455 |
| rs571032573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489189 | GCGCCCAGCGTATTT[A/T]GCGAACGGACAAGCA | 51455 |
| rs571039597 | snp | C/T | 3.39138e-05 | 0.00411774 | intron-variant | REV1 | GRCh38.p7 | 2:99410871 | TGCCTCTTTTGGCTA[C/T]GGAAAGACAAACGTG | 51455 |
| rs571050368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412089 | GTACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 51455 |
| rs571066180 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462020 | TACTTCCTAAACTGT[A/G]AGAATTCAGGTCCTT | 51455 |
| rs571157644 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99430108 | TCTAATAAAAGAAAA[-/CT]CTAAAATGGTTCGCT | 51455 |
| rs571165059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99410291 | GCTGGGATTACAGGT[A/G]TGAGCCACCACACCT | 51455 |
| rs571383281 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405230 | TGCCAGGGCCTACCT[A/G]TGCATCCACATCTGG | 51455 |
| rs571437471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99428550 | AAATATAAGCATGCA[C/T]GTTTGAACTTAATGC | 51455 |
| rs571502635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481399 | TATCAATAAAAAAAA[A/T]GTTATGTAGTAATTC | 51455 |
| rs571505349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99423119 | CTCCTACATAATGAC[A/G]CCAGGAAATAATCAG | 51455 |
| rs571526459 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99445424 | TGACCATCTAATCAC[A/G]GGATATACAAATATA | 51455 |
| rs571530300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437197 | TGTGTTGCCCAGGTT[A/G]GTCTTGCACTCCTGG | 51455 |
| rs571550809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99472841 | TCCAATGTGCTCTTA[C/T]TCTGTCCTTTAATGG | 51455 |
| rs571561813 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99436096 | AGATTATTTCTATCA[A/C]CTCAAGAGAAGCCAA | 51455 |
| rs571570184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444890 | TACTGACATTTTCTA[C/G]TATTCTTTCAAAACC | 51455 |
| rs571622239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99414671 | TATTTCTTTTTTGTC[A/G]TAAGACTTCTTAACA | 51455 |
| rs571631929 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99422221 | TATCTACACTCTCTG[A/C]ATGTGGACATACTTT | 51455 |
| rs571731915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483011 | GACAAGGGCAAAACT[A/C]CGTTTCAAAAAAAAA | 51455 |
| rs571732417 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | REV1 | GRCh38.p7 | 2:99428968 | CTGCACTCCAGCCTG[A/G]GTGACAGAGCGAGAC | 51455 |
| rs571741616 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99450342 | CATTACTAGCATCAC[A/T]TTAATCATCACTGTT | 51455 |
| rs571758529 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99429475 | AGTATGGATTACAAG[A/G]TTTTTTCTTAGCAAT | 51455 |
| rs571778448 | snp | A/C | 6.19444e-05 | 0.00556492 | intron-variant | REV1 | GRCh38.p7 | 2:99449285 | AATAAATAAATAAAA[A/C]GTATTCTAACTTTAA | 51455 |
| rs571791464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482206 | ATGCTGTAGAGTAAG[C/T]GAGGTTTCCTGGCTG | 51455 |
| rs571817158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457328 | CGAACTGATCTACAG[A/G]TTTAATGTAATTCCT | 51455 |
| rs571830207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489416 | ACTGAATGGCCGGCC[A/G]AGGCGCCGGCGCAGG | 51455 |
| rs572103113 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99410493 | ATGCCGTCAAACCAA[A/C]CTCCTGTGTGTGGGC | 51455 |
| rs572117461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99465502 | CAGAAAAGATTATCA[C/T]TGATAATAAACTATA | 51455 |
| rs572151671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411029 | CGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 51455 |
| rs572153339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404118 | ACAGGGACTCAGGTT[A/G]TTACTGTCCCCCATG | 51455 |
| rs572164183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418722 | AAGACTTAAAAATTT[C/T]TATATTCATGTCTGG | 51455 |
| rs572230488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481546 | AAGTGTCTGTTCTCA[A/C]TTCTTTAGCCAGCAT | 51455 |
| rs572252997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472257 | CAAAGCGTGCTACAA[C/T]TTGCATGAACCTTGA | 51455 |
| rs572265975 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480859 | AAAATTATATACTTT[A/T]AAAAAAACAAAAACA | 51455 |
| rs572315682 | snp | A/C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460321 | ACCTTGTGATCTGCC[A/C/T]GCCTCGGCCTCCCAA | 51455 |
| rs572326762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470984 | TTTATGTAATAGTTA[A/T]CTAAGAAATATTTAC | 51455 |
| rs572338901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417191 | GTCACCCATGCTGGA[A/G]TGCAGTGGTGCGATC | 51455 |
| rs572365741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99412162 | CTCTTGAATCTGGGA[A/G]ACGGAGGTTGCAGTG | 51455 |
| rs572395090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99479088 | TAATCCCAGCACTTT[A/G]GGAGACCGAGGTGGG | 51455 |
| rs572404077 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99488704 | GTGGACAGATAGATG[G/T]TTCCCACAGGCTGAT | 51455 |
| rs572404134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480041 | AAAACATAAAAGGGC[C/T]GAGTGCAGTGGCTCA | 51455 |
| rs572471451 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | REV1 | GRCh38.p7 | 2:99473241 | GGAGTGGTGGCGCAT[A/G]CCTGTAGTCCCAGCT | 51455 |
| rs572483096 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484569 | CCAAGACACATGATT[C/T]TTTGACTTATTTTTA | 51455 |
| rs572487383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99473848 | AAGTAAGTATGATCT[C/T]TCCATCTTTTCTTGG | 51455 |
| rs572489853 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99487198 | GGGGTAGGTTGCTGA[A/C]AGTCAGTCACCTAGT | 51455 |
| rs572492219 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99420339 | TCTTACCTGGAAGCA[C/T]ACTTGTCATATGCAA | 51455 |
| rs572498821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99421350 | TTATATTTCCAGCAC[C/T]TATCTCGTGTGTCAC | 51455 |
| rs572603264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99419870 | ATATTGAGGACATAT[A/C]TTGGTTTTATAGAAG | 51455 |
| rs572619042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99435700 | CCTTCCCTGATAATC[A/G]AATATAGAAAATTTG | 51455 |
| rs572671433 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427940 | TATAAAGGTAAATTT[A/C/G]TATTTACCGTGGGTA | 51455 |
| rs572684665 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99427231 | TGTCCATTCTACATA[A/C]TAAAATACATCCATA | 51455 |
| rs572751344 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469087 | GTTCGACTGCAGAAT[C/T]TTTGTGGGGCCATGA | 51455 |
| rs572769683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437832 | TTGACTAAAAGCACA[C/T]AGGAATACATCAAAC | 51455 |
| rs572796748 | in-del | -/ACTCCACCCTGGGCAACAAAGTGAG | 0.00835141 | 0.0640778 | intron-variant | REV1 | GRCh38.p7 | 2:99412198 | AGACTGCGCCACTGC[-/ACTCCACCCTGGGCAACAAAGTGAG]ACTCCACCCTGGGCA | 51455 |
| rs572808878 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99453766 | GGCATGGTAACACGC[A/G]CCTGTAGTCCCAGCT | 51455 |
| rs572835861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474818 | GAGGCACGACAATCA[C/T]TTGAACGCGGTAGGC | 51455 |
| rs572835935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483207 | AACTTAATGAAAACC[A/G]TTTAAAAGAGCAAAA | 51455 |
| rs572840035 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443375 | ATATGTTTCTTATTG[C/T]CTCATAAATCCAAGA | 51455 |
| rs572851543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437335 | AACATCATGGACTAT[C/T]TATCACTTCTATTCA | 51455 |
| rs572915116 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99449879 | CTATAAACCCATTTA[C/T]GAATCATTTTACAAA | 51455 |
| rs572923457 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | REV1 | GRCh38.p7 | 2:99489781 | TGTCCGATCCCGCCC[C/T]TCCCCCACCCCGCCG | 51455 |
| rs572931795 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99402064 | ATCACATGTAAGACC[C/T]TGAGGGCAACATATT | 51455 |
| rs572932848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447245 | CATTGTAACCTTTGT[C/T]TACTGCAACCTCTGC | 51455 |
| rs573036879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99406165 | GCAGGGCCTTTAATC[C/T]TCTGTCCATTACAAA | 51455 |
| rs573058333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99415088 | GGGAGGGAGGCAGGG[C/T]ATGTGGTGTACCTCC | 51455 |
| rs573088136 | snp | C/T | 8.25239e-05 | 0.00642302 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403032 | TCCTTTTTGGTGAAC[C/T]AATGGTTTTTTTCTT | 51455 |
| rs573108203 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443546 | AGATTCTAAAAACGG[A/T]ACTATATATGATACA | 51455 |
| rs573118226 | snp | A/G | 0.000164891 | 0.00907846 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412749 | AGTAAACCTTATTCC[A/G]TAGTTGATCTCAGCT | 51455 |
| rs573146600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99452006 | GGTTCTATTTCTTCA[A/G]TACTAGAACATACTC | 51455 |
| rs573148559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459687 | CTACAGCCTGGGTGA[C/T]AGAGGGAGACCCTAT | 51455 |
| rs573154933 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99445586 | TGGGCCAGTGGGGTA[C/T]GTCATAGCAGCTTCT | 51455 |
| rs573158673 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491526 | CTGACCTCAGGTAAT[A/C]CACCAGCCTTGGCAT | 51455 |
| rs573231173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99422642 | AAGCTGCCCTGAGAC[A/G]GGGAGAATATGAAGC | 51455 |
| rs573268477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461859 | GAAACTGTGCAACAG[G/T]CAAAGAAGCATTTGC | 51455 |
| rs573278831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99437241 | TCCCGCCTCGGCCTC[A/C]GAAAGTGTGCGAATT | 51455 |
| rs573302517 | snp | C/G | 1.69622e-05 | 0.00291219 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408033 | TATATACTTACCCCT[C/G]TCATATCTGATATAT | 51455 |
| rs573311229 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99468146 | GATTGCACCATTGGA[-/C]TCCAGCCTGGGCAAC | 51455 |
| rs573317338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99436719 | TAACCCTAATCCAGG[A/C]ACAAGCAGAGCTTTC | 51455 |
| rs573344599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407413 | AAAAATTAGCTGGGC[A/G]TGGTAGCGGGTGCCT | 51455 |
| rs573357957 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401052 | TATGCTACAGTAAAA[G/T]AATTAACACAATTAT | 51455 |
| rs573405632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99414366 | GAAGTGAGATGAAGG[C/T]GTTAAGCGTGCTCGT | 51455 |
| rs573406420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99469399 | TCTCCCAACCCTCGA[A/T]AGGTTCACAAGCTAA | 51455 |
| rs573421677 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400346 | TATTTGGGCTTAGTG[C/T]TTCTAAATTGTTGCA | 51455 |
| rs573434285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99461021 | ATGTAAGAAGCAATG[C/T]CTGTTTTCATTAACG | 51455 |
| rs573469182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99468880 | ATCGAGTGAGACTAC[A/G]CACGTGGAAACCCTT | 51455 |
| rs573470141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99464144 | ACCTCACAATAAATA[C/T]TAAAAAATAATTTTT | 51455 |
| rs573495113 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99406737 | AATATACCAAAAGAT[A/C]TTTAAAATCAGAAAA | 51455 |
| rs573500282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99444112 | GGTGTGAGCCACCGC[A/G]CCCAGCCCTTTTCTT | 51455 |
| rs573600834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99475635 | GAGATTGCAGTGAGC[C/T]GAGATTGAGCCACTG | 51455 |
| rs573633263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444484 | AAGGGTGTCAGGCCT[C/T]ATCCAGCTCCTAACA | 51455 |
| rs573641687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99489489 | CGGCCGGGCGCGGAG[A/G]GAAGGGCCGCTGCGC | 51455 |
| rs573650919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99406844 | GAGAGGACAGTCTAC[C/T]TGGAAACTTCACTAT | 51455 |
| rs573761380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99460934 | TTTCTTCCCTCACAC[A/G]AAGAATCTCTTTTTC | 51455 |
| rs573797815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459887 | GGTATAGGGACTACG[A/C]AATCATGAGAGGCTC | 51455 |
| rs573870874 | in-del | -/A | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490707 | TCCCGCAGGGCACAG[-/A]CACTATCTTCTGTCC | 51455 |
| rs573901718 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99484826 | TTAAGGTGTCCCACA[A/G]CAGACCGGTTATGAC | 51455 |
| rs573907033 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99459084 | GTGGTGGTGGCCACC[G/T]GTAGTCCCAGCTACT | 51455 |
| rs573937084 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99468208 | AAGAAAGAAAGAAAA[A/C]TTAGCCAGGCATGGG | 51455 |
| rs574017444 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403981 | TCTTCAAAATGGTTA[A/G]AGCAAGAATAAGGAA | 51455 |
| rs574034748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99429031 | GTAACTGATCTAAGA[C/T]TCTGTTTCGATTTGA | 51455 |
| rs574051446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408259 | GAAGATTATAAAAGT[G/T]AATGCCATAGTCTCC | 51455 |
| rs574051521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468765 | ATGAAGAGTGAATAC[A/G]TGAATGCAAAAGTAC | 51455 |
| rs574166697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99407348 | CTGAGGTCAGGAGTT[C/T]GAAACCAGCCTGGCC | 51455 |
| rs574205289 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467947 | GCACTTTGGGAGGCC[A/G]AGGTGGACAGATCAC | 51455 |
| rs574234238 | snp | A/C | 3.64924e-05 | 0.0042714 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406464 | GTTCAGATTAGTTGG[A/C]ACCAACTGATTCACG | 51455 |
| rs574253653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448774 | GTGCACACATATTTG[C/T]TGAATAACACGCTTG | 51455 |
| rs574264981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99474092 | CCTATTAACTGACAC[A/T]TTATATTTCCTTCCT | 51455 |
| rs574268709 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468361 | CCCTAGAACGGAGGA[A/G]GGCATTTAATCAGGA | 51455 |
| rs574345765 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419373 | GCCCACCACCATGCC[C/T]GGCTAATTTTTCTGT | 51455 |
| rs574359224 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415912 | AAACTGTAATAGTCG[C/T]TGGGGTCAATCCTTT | 51455 |
| rs574388613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470128 | TCCATCTCAAAAAAA[A/G]AAAAAAGATATTTCA | 51455 |
| rs574394952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99415325 | GAATCAAATCTCAAC[A/G]AAGAGAGAGTCAAGG | 51455 |
| rs574425278 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99477211 | AGAGACTACATTTCC[A/C]ACGCTCCTCTCAAAA | 51455 |
| rs574460376 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99469665 | AAGAGTCTCATCAAG[A/G]ACATGCTTATTTAAA | 51455 |
| rs574472236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433649 | TTCTGGGTAATATAT[C/T]TCTGAGAAACTAATT | 51455 |
| rs574499662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99476429 | GGCATGGTGGCACAC[A/G]CCGGTAATCCCAGCT | 51455 |
| rs574507456 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99424510 | CCAACTATGTCATTA[A/T]AATACCAGGTTTGGC | 51455 |
| rs574509332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432664 | TCTTTTTCTAGTGAC[A/G]GGACAATCTCCTTTT | 51455 |
| rs574532136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461952 | GACAATAGGCACAGC[C/T]GGTGGGGAGGAGGTA | 51455 |
| rs574561963 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439313 | AACGATGTGATTTCT[A/G]AAGCAGGAAAAAATT | 51455 |
| rs574663004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99430727 | ACACTCTGGAGAGCC[A/T]ACTGGCTGCATGCCA | 51455 |
| rs574682630 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462033 | GTGAGAATTCAGGTC[C/T]TTTCCTTCCCTGCTT | 51455 |
| rs574738186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99438075 | GTATGCTACTGTGTG[G/T]GCATTTGTTTTTGAT | 51455 |
| rs574795766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440840 | CCTTTACATGCATTA[C/T]AGCAACACATGCAAC | 51455 |
| rs574816554 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99456002 | CTCTTTCCATATGAA[A/C]TGTCCCAATCTCACA | 51455 |
| rs574851157 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99457039 | AAGCTAAACATTTCG[-/A]ATTCCTTTATGAAGT | 51455 |
| rs574925251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99448305 | ATAAAATTACTACTT[C/T]AATATTTTACTTCTT | 51455 |
| rs574970448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440407 | TTCCACCTAAAGCCC[C/T]TCACCCTAATACCAA | 51455 |
| rs574985137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99485631 | GTGGGCGGTTGTTGA[G/T]ATAATCACTCTTAGC | 51455 |
| rs575007115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99447863 | GTAACCGGGATTACA[C/G]GCACAAGCCACCACT | 51455 |
| rs575079701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408918 | AATATTCCCAGAAAA[A/G]ATTATTATAAATTGA | 51455 |
| rs575166130 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99425336 | ATAAAAATAGTAATA[C/T]TATAAATGGTCTCAG | 51455 |
| rs575197044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99422755 | GTCTCCAGCCTTCTA[C/T]TGGGACCGTGTGCAT | 51455 |
| rs575209315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431509 | AAAAAGGAGTGCTGA[A/G]GCTTGAACAGCCACA | 51455 |
| rs575230021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484153 | ACCACATGTTCTCAC[C/T]TGCAAGTGGCAGCCA | 51455 |
| rs575251160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440288 | ATTCTACTTAGGAAT[A/G]TCCAAATGTCCATAG | 51455 |
| rs575314972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483300 | CCATTCCTAGAAATA[A/G]CAAATGTAGAAATGA | 51455 |
| rs575316111 | snp | A/G | 0.00166358 | 0.0287927 | intron-variant | REV1 | GRCh38.p7 | 2:99403648 | GACAACAGTGACTCC[A/G]TTACTCTTTGTCTTC | 51455 |
| rs575353421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99468895 | ACACGTGGAAACCCT[C/T]TGAAAACTATAACAC | 51455 |
| rs575384501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99408789 | AGAATTACTAACTCA[G/T]TAACAGATTAACAAA | 51455 |
| rs575389936 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | REV1 | GRCh38.p7 | 2:99475697 | GTCTCAAAAAAAAAA[A/T]AAATAGGCCAGGCAC | 51455 |
| rs575412684 | in-del | -/ACTC | 0.00318978 | 0.0398085 | intron-variant | REV1 | GRCh38.p7 | 2:99410967 | TTAAACATGTTGGTT[-/ACTC]ACTATCACGCTCAGC | 51455 |
| rs575446088 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99490021 | CCGCGGTGGCTCTCC[A/G]CCCCTCCCCCTCCGG | 51455 |
| rs575504925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99453308 | AGGTTGCAATGAGCT[A/G]AGATTGTGCCACTGC | 51455 |
| rs575548280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99484832 | TGTCCCACAGCAGAC[C/T]GGTTATGACCTCGGG | 51455 |
| rs575583593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99445181 | TCATGAGAGATAAAA[C/T]TGCAATCAACTTTTA | 51455 |
| rs575606396 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468561 | AAAAATTGCCTTCTA[C/G]TTTTCAGAGGAACTC | 51455 |
| rs575643154 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466303 | GCTGAAGTGCAGTGG[C/G]ACGATCTCGGCTCAC | 51455 |
| rs575686625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99401733 | GCCTGGGCGACAGAG[A/T]GAGACTCCATCTCAA | 51455 |
| rs575739001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99463711 | CTCACTGCAAACTCC[A/G]CCTCCCAGGTTCAAG | 51455 |
| rs575875161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99470879 | TGCAGAAAGTATAAA[A/G]ATGGCCTTGCTGAGG | 51455 |
| rs575935844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99449145 | TGGCGCCTGCCTGTA[A/G]TCCCAGCTACTCTGG | 51455 |
| rs575974553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457295 | AAAACTCAACATAGT[A/G]AAGATGTCAATTCTC | 51455 |
| rs575976331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99461907 | CCAAGAATAAAGACT[A/G]CACTACCCCTTCCAG | 51455 |
| rs576012046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99469536 | ACTAGCCAGGTGAGG[C/T]AAGGTTAAGGCAAAT | 51455 |
| rs576042975 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99426786 | CTTCGTTAAGTGTAT[A/G]CTGCAAAAACAGCTT | 51455 |
| rs576051662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99456389 | ACCATTTTAGGTGCA[A/C]ATAAATGAAGAGGAA | 51455 |
| rs576058609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99403448 | TTTAAGACATTTGTG[C/G]TAATGTCCTATTCCA | 51455 |
| rs576158894 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | REV1 | GRCh38.p7 | 2:99425423 | AAAGAAAACAATTCT[G/T]GATGTGTCGAGGACT | 51455 |
| rs576162409 | snp | A/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490471 | AGTGGGGAAGGACAC[A/T]AGTGCAGACACTGAC | 51455 |
| rs576180712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99487527 | AACCTAATTGCCTCT[A/G]AAGAGCCTTTTTAAT | 51455 |
| rs576254691 | in-del | -/C/CAC | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481710 | CACACACACACACAA[-/C/CAC]AAATTTAAATTAGCC | 51455 |
| rs576300279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99477386 | AATAAGGACAATACC[C/G]TATGGAAGGGCTAAG | 51455 |
| rs576317071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486390 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGTGCCT | 51455 |
| rs576320817 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99471806 | AAGCACACAAAAAAA[-/C]GTTCAGTGTCATTAA | 51455 |
| rs576322594 | snp | C/G | 0.000121352 | 0.00778853 | intron-variant, missense | REV1 | GRCh38.p7 | 2:99424804 | GACCAATTCCATGCT[C/G]CTGAAGTGGCTCCAC | 51455 |
| rs576373685 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416702 | GAGGCCGAGGCGGGC[A/G]GATCATGAGGTCAGG | 51455 |
| rs576421724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99473138 | TGGGAGGCTGAGGTG[A/G]GCAGATCATTTGAGG | 51455 |
| rs576435399 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99472494 | GTACTTAATGTGACT[C/G]AACAGTTAAAATGGT | 51455 |
| rs576458636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480672 | CCTCAGAGCAACTGC[A/G]ATTCAAAAATATAGT | 51455 |
| rs576496903 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99427188 | CTTCATCTCTGGGGG[A/G]AAAAAATTGCCATCA | 51455 |
| rs576498230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99466411 | CCATGCCTGGCTATT[C/T]TTGTATTTTTAGTAG | 51455 |
| rs576512615 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | REV1 | GRCh38.p7 | 2:99470738 | AACAAATACAGAATG[A/T]GAGGTCCTGTTCCAG | 51455 |
| rs576545761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99465819 | TACCATATGAAGCCT[C/T]ATATATTATCCACGT | 51455 |
| rs576557543 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463132 | TACATAAAACACATA[C/G]GTCAAAGAAGAATTT | 51455 |
| rs576629202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450260 | GAAAATATCTTAAAG[A/T]CACAATGTGACTTAT | 51455 |
| rs576652192 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99403606 | TGCAACAGCTTAGAC[-/TT]TGCCCATTATATACT | 51455 |
| rs576658541 | in-del | -/TG | 0.00755907 | 0.0610114 | intron-variant | REV1 | GRCh38.p7 | 2:99431435 | TCTAAGCTGAAAAAC[-/TG]TAAGAATTTCAGGAC | 51455 |
| rs576723123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99442792 | AGATAAATAAACTGA[A/C]TAAGGATGCTCAATT | 51455 |
| rs576725178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99433994 | TCATACAAATCTTGA[C/G]CAAGACAAACTTTAA | 51455 |
| rs576737222 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413583 | TCTCTGAAGAGATAT[G/T]AACTCTCCTACAGCT | 51455 |
| rs576807286 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | REV1 | GRCh38.p7 | 2:99463649 | TTATTTTTTTGACAG[A/G]GTCTTGCTGTTGTCG | 51455 |
| rs576818751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99418087 | GTTAACAGAAACTTC[C/T]AAGTTAGTTCGGACA | 51455 |
| rs576831366 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99409680 | GAAACCCTATCTCTA[A/C]TGAAAATACAAAAAT | 51455 |
| rs576854242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99462706 | AATTTTAAAAACTAA[A/C]TAAATAAATGGACCT | 51455 |
| rs576893868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99458364 | CATTATTAGCCACGA[A/G]GCAAATGCAAATTAA | 51455 |
| rs576908541 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99469755 | CACTACTATCAGTTC[A/C]TTCTAAACTTTATTC | 51455 |
| rs576932678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99417004 | GTCAAGTAGCTAAAA[C/T]GTCCCTATTTCTATT | 51455 |
| rs576983970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99431475 | TCACACTTCAACAGA[A/G]GGTGCTACTAGACCC | 51455 |
| rs577022400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440198 | CCTGGCTCCTCTAGA[C/T]GTTTGTTTAGAAATG | 51455 |
| rs577026104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99430872 | AAAAAAAAAAATCAC[A/G]TTCTAAAACCACAAC | 51455 |
| rs577042626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99425379 | AGTAGATAAGAAATA[C/T]CTAAGAGGAAGGAAA | 51455 |
| rs577053197 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415670 | CTTTAATTTAACTCA[C/T]ATTGTACTAGCTTCA | 51455 |
| rs577058170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484682 | TAAGTATAGTAGTAG[A/T]AGTTAAATCTAAAAA | 51455 |
| rs577105743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99424737 | ACACAAAACAGTGCT[A/G]TGTGACAAACAGACA | 51455 |
| rs577188990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99434640 | TTAAGTTTCTTAGCA[A/C]CTCCAGAAAAGCCAA | 51455 |
| rs577217153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99444371 | GTGCAAGGAACAAAA[C/T]GCCCTATGATCATTC | 51455 |
| rs577226643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433799 | CACATGAAAATCTTA[A/G]TAAGTATTATGACTA | 51455 |
| rs577262791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99487314 | TGCTTTTAGAGGACA[C/G]TAAGCAAGAAAGTGA | 51455 |
| rs577265655 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479934 | CTAAGAACAATCAGT[A/G/T]GGATTTTACAGGATA | 51455 |
| rs577267569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99471773 | CACTTCTCTAAAGAA[C/G]ATAGACAAATGGCCA | 51455 |
| rs577293387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99451056 | ATTAAACAGCTAGCC[A/G]GTCAGGAATCTACAG | 51455 |
| rs577298496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99486315 | CGGGCGGATCACGAG[G/T]TCAGGAGACCGACAC | 51455 |
| rs577328294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99450452 | CACATGTGGCTTATC[A/G]CAAGCTTAATCCCAA | 51455 |
| rs577380648 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456524 | TGAATGATGAAGACC[C/T]GAGGAAGCAGAAGGA | 51455 |
| rs577410948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99479174 | CTCTACTAAAAATAA[A/T]AAAATTAGCCAGGTG | 51455 |
| rs577433685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99411103 | GACCAGCCTGGCCAA[C/T]GTGGTGAAACCTCAT | 51455 |
| rs577479568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99456323 | CAAGTCTGTGCCCCG[C/T]GATAGCACTTGTATT | 51455 |
| rs577530880 | in-del | -/AACT | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99450547 | TTCTAGAAGATAAAA[-/AACT]AACAGCACATACAGA | 51455 |
| rs577556355 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99441071 | AGATTTTGAAAAAAC[A/G]TATCTATTTTCTACT | 51455 |
| rs577657147 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99410226 | ATGTTGGCCAGGCTG[C/G]TCTCAAATTCCTGGC | 51455 |
| rs577678411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99458853 | ATTAGTGGTTGCCAG[C/G]AGTTAAGGAAAGGCG | 51455 |
| rs577700621 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407255 | CCACCACACCCGGCT[A/G]ATTTTTGTATTTTTA | 51455 |
| rs577708688 | snp | A/G | 1.66186e-05 | 0.00288254 | intron-variant | REV1 | GRCh38.p7 | 2:99404694 | TATAAAATGCCAAAC[A/G]TATGAGTAGGAAGTT | 51455 |
| rs577718772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99404150 | AGGATTATACATCTC[C/T]GCTCTGTTGTATTCA | 51455 |
| rs577720973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99467170 | GTAACGTCTGTTGTA[C/T]ACCTACTGCACAAGG | 51455 |
| rs577767878 | in-del | -/A | 0.49823 | 0.0296997 | intron-variant | REV1 | GRCh38.p7 | 2:99452421 | AGCCAGAGCCTGTCT[-/A]AAAAAAAAAAAAAAA | 51455 |
| rs577779284 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436998 | TTTTTTGTTTTTTTT[-/G]TTTTTTTTGAGATAG | 51455 |
| rs577808971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99457902 | CACCAAAATATGCCT[A/G]ACTGACTGTGTTGCA | 51455 |
| rs577814278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | REV1 | GRCh38.p7 | 2:99466099 | GGTGCCCGCCACCAC[A/G]CCCGATTATTATTTT | 51455 |
| rs577823085 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | REV1 | GRCh38.p7 | 2:99451844 | TTCAACAAAAACAGA[C/T]CTGCCAATAGTGCAC | 51455 |
| rs577843617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | REV1 | GRCh38.p7 | 2:99465580 | ATACTATAAAACCAC[C/T]AGGATGACCAAATGA | 51455 |
| rs577867228 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | REV1 | GRCh38.p7 | 2:99464272 | AGGTGTAGGTGGCTA[-/G]AAGTACATGATGTTT | 51455 |
| rs577924277 | snp | A/G | 1.70528e-05 | 0.00291995 | intron-variant | REV1 | GRCh38.p7 | 2:99406299 | TAAGCAGCACCTAAA[A/G]AAGAACCACATTGAT | 51455 |
| rs577970215 | snp | C/G | 1.90015e-05 | 0.00308227 | intron-variant | REV1 | GRCh38.p7 | 2:99405868 | TTGTATTTATATTTA[C/G]GAGTATAAAATGTAC | 51455 |
| rs578008550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99459162 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 51455 |
| rs578015037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99472413 | TACTGTTTAACAGGT[A/G]GAGTCTCAGGCAAGG | 51455 |
| rs578083191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99413175 | TGGACTCCACATATA[A/G]ATGAACCAGAAACTT | 51455 |
| rs578161825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | REV1 | GRCh38.p7 | 2:99427952 | TTTATATTTACCGTG[A/G]GTAAATATAAATGCA | 51455 |
| rs578162422 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | REV1 | GRCh38.p7 | 2:99412190 | GTGAGCCGAGACTGC[A/G]CCACTGCACTCCACC | 51455 |
| rs578182843 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481669 | GGAGTCTGAAACCAG[A/C]CTGGGCAACATGGGG | 51455 |
| rs578200514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481034 | AATATGCAAAAGAAT[A/G]TTAACCTCCAACACA | 51455 |
| rs578211811 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | REV1 | GRCh38.p7 | 2:99489100 | AACACAGCGCGGCTC[C/G]GTGCGCCCAGAGCGG | 51455 |
| rs578237069 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99471631 | GCAATCCACAGAATG[A/G]GAGAAAATATCTGCA | 51455 |
| rs745313025 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475485 | TAAGAGAAGTTACTA[-/T]TTTATTTCTAATCAG | 51455 |
| rs745367461 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416337 | CACCACAGAAGGTTC[C/T]CTCTCCTATATGAAA | 51455 |
| rs745379675 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403723 | TGACTGCTGGTGAGT[C/G]CTGTTCTCGCCCTGC | 51455 |
| rs745392068 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99452307 | TGGTGTGTGCCTGCA[A/G]TCCCAGCTACTAGGG | 51455 |
| rs745392791 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99441052 | TCCTAAAGTGTCACA[A/C]AGAAGATTTTGAAAA | 51455 |
| rs745397875 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477808 | AACTACCAAAAAAAG[A/G]TGCTTGATTTAACAA | 51455 |
| rs745403127 | snp | C/G | 1.64776e-05 | 0.00287028 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442366 | GACCTGGCAGAGGAT[C/G]CTCAGGTCTGCATAC | 51455 |
| rs745478315 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437349 | TCTATCACTTCTATT[C/T]ACAAAGAAAACTAAG | 51455 |
| rs745483646 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99415106 | GTGGTGTACCTCCAA[A/C]TCCTATTGAGTGGGG | 51455 |
| rs745495113 | snp | C/T | 1.65411e-05 | 0.00287581 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424273 | TTCCGTTCTTAATGC[C/T]AAGTTGCCTAGAGCG | 51455 |
| rs745571644 | snp | A/G | 1.75265e-05 | 0.00296023 | intron-variant | REV1 | GRCh38.p7 | 2:99407993 | TGAGAGATACATTAC[A/G]CAAAGTCAGAATTTA | 51455 |
| rs745583531 | snp | C/T | 2.3697e-05 | 0.00344208 | intron-variant | REV1 | GRCh38.p7 | 2:99403144 | TCCTCAACAAAATGA[C/T]AGTATGGATAGTCTG | 51455 |
| rs745633151 | snp | A/G | 3.29766e-05 | 0.00406045 | intron-variant | REV1 | GRCh38.p7 | 2:99464995 | GAGCTTCTGTATTGG[A/G]GAGGAAAAAAAAAAT | 51455 |
| rs745666361 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99424407 | TCCATTCTCATTAGG[G/T]ATTAAAGATAGGCAT | 51455 |
| rs745671872 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470284 | TAACTCTAAAGTCTG[C/T]TGATTAACTAATGAA | 51455 |
| rs745678480 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482495 | TTGTAGCTAATATAA[A/G]AAGTGAGGAGAGTCT | 51455 |
| rs745680673 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456836 | GAAGTGAGGAGGGAA[C/G]GAGTTTTTCCTCAGA | 51455 |
| rs745745968 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416701 | GGAGGCCGAGGCGGG[C/T]GGATCATGAGGTCAG | 51455 |
| rs745761519 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460162 | GCTCACTTCAACCTC[C/T]GCCTCCCGGGTTCAA | 51455 |
| rs745772943 | snp | A/C | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412855 | CCTGTTTTGGGACCA[A/C]ATTCTTTTTGGAGTT | 51455 |
| rs745784871 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469061 | TAACATTTCTTCATC[A/T]ATAAAACAAAGTTCG | 51455 |
| rs745790636 | snp | A/G | 1.65078e-05 | 0.00287291 | intron-variant | REV1 | GRCh38.p7 | 2:99435831 | ATAAGCAAGAATACA[A/G]ACCTTTGAGATCTGG | 51455 |
| rs745843170 | in-del | -/T | 1.65105e-05 | 0.00287315 | intron-variant | REV1 | GRCh38.p7 | 2:99465010 | GGAGGAAAAAAAAAA[-/T]GTCAATTTTATAACA | 51455 |
| rs745844273 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411801 | ATGTGTGTTCCAACA[C/G]TGTGCTTACAGCCCA | 51455 |
| rs745848964 | in-del | -/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481893 | TGACTGGCCATTGTC[-/T]TGATTCCTGGAAAAC | 51455 |
| rs745862904 | snp | A/C/G/T | 5.01153e-05 | 0.00500557 | intron-variant | REV1 | GRCh38.p7 | 2:99418791 | AAAGTACTTGTAATG[A/C/G/T]CTGTAATAAAAGTAT | 51455 |
| rs745874309 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481666 | CCAGGAGTCTGAAAC[C/G]AGCCTGGGCAACATG | 51455 |
| rs745879835 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99414697 | AACATCAGGGAAGAC[-/T]TTTGTGTCTCTCTTT | 51455 |
| rs745887710 | snp | C/T | 1.65141e-05 | 0.00287346 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439078 | TGGCAACACTGTTGA[C/T]CATGGGCACCAAGCA | 51455 |
| rs745887812 | snp | A/T | 1.77219e-05 | 0.00297668 | intron-variant | REV1 | GRCh38.p7 | 2:99429817 | TTATTCATTAAGAAT[A/T]GTAACACACAACTTC | 51455 |
| rs745911239 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476892 | AGTTTCGTAAGTGGA[C/T]TCTTCTGTGTGCCCC | 51455 |
| rs745958552 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432297 | GTCCTAATACTTTGT[C/T]TAGACATATAAGCCA | 51455 |
| rs745974787 | snp | C/T | 1.72934e-05 | 0.00294048 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429941 | CAATGATGAATCTGG[C/T]ATATCTGCTTTAAAA | 51455 |
| rs745994494 | snp | A/G | 1.69473e-05 | 0.0029109 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410703 | AGCTTACCTGGCAAT[A/G]TTATCACAAATTCCA | 51455 |
| rs746026594 | snp | C/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402733 | GCTGGAGGTCTCACA[C/G]AGCCAGCTGGGTCAG | 51455 |
| rs746034453 | snp | G/T | 4.27058e-05 | 0.00462072 | intron-variant | REV1 | GRCh38.p7 | 2:99406116 | GAAATACTACAAAAA[G/T]AAAATATATAAAATA | 51455 |
| rs746052291 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433764 | CTCAGTGAATTTACT[C/T]AGGGGAAAAAAGCAA | 51455 |
| rs746053416 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461611 | TCACTTCAAAAAATA[C/T]AATGAAATGATAAGA | 51455 |
| rs746060713 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452869 | TATTAAGAGGACAGA[C/T]TCCAAAGCAGGAATG | 51455 |
| rs746082931 | snp | A/G/T | 0.000395919 | 0.0140644 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439001 | CAGAGTGCAGTCTCT[A/G/T]AAATCAGTGCTGCTC | 51455 |
| rs746150036 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99455816 | AAATCCTTATTTGAA[A/G]TATAAGTCTGTTACA | 51455 |
| rs746152013 | snp | C/T | 1.67061e-05 | 0.00289011 | intron-variant | REV1 | GRCh38.p7 | 2:99435985 | CCAAGCTAATTTTTA[C/T]TATTTAAAACATCAG | 51455 |
| rs746159674 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99475053 | AAATGCTTGTTCCCC[A/G]GTGCCATAAAGAAAC | 51455 |
| rs746167963 | snp | A/G | 2.55157e-05 | 0.00357172 | intron-variant | REV1 | GRCh38.p7 | 2:99449554 | TATGTGTAAGAAGTA[A/G]AACCCTAATGAATAA | 51455 |
| rs746221037 | in-del | -/A | 0.042547 | 0.139511 | intron-variant | REV1 | GRCh38.p7 | 2:99418952 | ATATTAGAACCTATT[-/A]AAAAAAAAAAGTCAT | 51455 |
| rs746229988 | in-del | -/AGTGCAGTCTCTGAAATC | 4.94996e-05 | 0.00497467 | cds-indel, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438989 | CTGCAACTGCTGCAG[-/AGTGCAGTCTCTGAAATC]AGTGCTGCTCTTCTC | 51455 |
| rs746243207 | in-del | -/TCT | | | cds-indel, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439291 | CATTTTCCGTTTCAA[-/TCT]TCTTAACGATGTGAT | 51455 |
| rs746246100 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99473558 | CATGTATTTAAGATA[C/T]CTTTTAAAAATATAC | 51455 |
| rs746250159 | snp | A/C | 1.66949e-05 | 0.00288915 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401218 | GCACAGCTATCAGAG[A/C]GCATCAGGCTCTCTG | 51455 |
| rs746254622 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404641 | CTACTTGTTCCCGGA[G/T]ATCAGGTGGAAGTGC | 51455 |
| rs746262876 | snp | G/T | 1.65745e-05 | 0.00287871 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438644 | GCCTGTTTTCATTTT[G/T]TTTAACTTTTCCCTT | 51455 |
| rs746290228 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455696 | AATATCTGGGAGGCA[A/T]TTATTTCCAAAAAAT | 51455 |
| rs746293834 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99422965 | GAGGATTTAAAGCAC[A/G]TTCCACTTGACAATA | 51455 |
| rs746330554 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407800 | CCCCTGGTTAATCAG[C/G]GGTACCTTGGAAAAG | 51455 |
| rs746333967 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487393 | TCCCTAGGGAACAGT[C/T]AGGGAGCAAGAGAAA | 51455 |
| rs746343527 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410811 | CATGCCAGTGGCTTC[C/T]AGTCTTCTTTGAATT | 51455 |
| rs746354888 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442390 | TGCATACAGGATTAA[A/T]GCTGAGACCTTTCTG | 51455 |
| rs746356148 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99456176 | TTTAGCATCTGAGTG[-/AA]AATATTTTAACATTC | 51455 |
| rs746419280 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443766 | ATACATTCAAAATTT[C/T]AGGTTACATTCAAAT | 51455 |
| rs746428956 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427745 | AACAGAAAATCACAA[C/T]TAAGGGACAAAAATC | 51455 |
| rs746429798 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99485586 | GATCTCCAGCTGAAC[C/T]TCAAAGGGAACTCTA | 51455 |
| rs746431720 | snp | C/T | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404556 | GGCAAAATTCCTGTA[C/T]TACAGCCATTTACTG | 51455 |
| rs746496753 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99404764 | CCACTTTAAATTTCA[A/G]TTTGAATACTGTGGA | 51455 |
| rs746503015 | snp | A/C | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491885 | TATAGAATACAGTAA[A/C]ATGGTATTAACTGCA | 51455 |
| rs746527048 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491485 | AGAGGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 51455 |
| rs746534994 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475272 | TTTGTTCCGATTGGC[C/T]AGCAACTTAGAACTT | 51455 |
| rs746539246 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99455275 | TTCACAATCTTATGA[A/C]TTAGAAAAGATAACT | 51455 |
| rs746548163 | snp | A/T | 1.6607e-05 | 0.00288153 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439274 | GCCATTGACTTTGAC[A/T]TCATTTTCCGTTTCA | 51455 |
| rs746639186 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421573 | GCAAATTCATCAGGA[C/G]TAAGTTTGGTCTCTG | 51455 |
| rs746684552 | in-del | -/AAAATAAAACA | | | intron-variant | REV1 | GRCh38.p7 | 2:99453918 | AAAAAAAAAAAAATC[-/AAAATAAAACA]AAAATAAAACAAAAC | 51455 |
| rs746695009 | snp | A/C | 0.021902 | 0.102329 | intron-variant | REV1 | GRCh38.p7 | 2:99421683 | CAAAGGCAACGAATC[A/C]CAGCCACAGCCACCA | 51455 |
| rs746695759 | in-del | -/TGAATTAC | 0.000231866 | 0.0107647 | intron-variant | REV1 | GRCh38.p7 | 2:99402233 | ATTTGATAAAAGTGA[-/TGAATTAC]TACCTTTTCATGTAT | 51455 |
| rs746711913 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99442145 | TAAGCCTAGCTACTC[-/G]GGAGGCTGAGGCAGG | 51455 |
| rs746725051 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99425834 | CTGAGAGGGGGAGTT[C/T]GAGACCACCCTGACC | 51455 |
| rs746725324 | snp | C/G | 4.94776e-05 | 0.00497357 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406364 | ATTTCTTAGCTTTCT[C/G]AACTTGGAAGACATC | 51455 |
| rs746726237 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468978 | ACAGTAGACTAGATA[C/T]GGACTCAAATCCCAA | 51455 |
| rs746740911 | snp | A/C | 1.65231e-05 | 0.00287424 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434427 | CCTGTGCCTCTGTTA[A/C]TTGTAACAGCCACTG | 51455 |
| rs746755036 | snp | C/T | | | intron-variant, upstream-variant-2KB, synonymous-codon | REV1 | GRCh38.p7 | 2:99479810 | AATAATAATACAAGA[C/T]CCTGCATTATAGGCA | 51455 |
| rs746797358 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481263 | ATACCAAAATTCAGA[A/T]TTTTTACAGCCAATT | 51455 |
| rs746885996 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99413360 | AAATGTAAGGGATCT[A/G]TTATGATTTCGGTCA | 51455 |
| rs746891372 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448661 | TTACTCATTCTTTCT[C/T]TCCCAACAGAATATA | 51455 |
| rs746908123 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480429 | AGGTGGAGAAATATA[A/G]CAGAAGGCCTTGAAT | 51455 |
| rs746938944 | snp | A/G | 1.69126e-05 | 0.00290792 | intron-variant | REV1 | GRCh38.p7 | 2:99434319 | TAAGACTTCAAAGAG[A/G]GCTCATTTGTACCTG | 51455 |
| rs746983808 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99399992 | CTGCTTTTTACTGCT[C/T]GTGTAGTCACGAGTC | 51455 |
| rs746986420 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403705 | CTCACCAGATGCGCT[A/G]GCTGACTGCTGGTGA | 51455 |
| rs747100898 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99435264 | AGAAAACACTAAGTT[A/C]TCTCTTTCAGACAGA | 51455 |
| rs747113289 | snp | A/C | 3.29973e-05 | 0.00406172 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438987 | TGCTGCAACTGCTGC[A/C]GAGTGCAGTCTCTGA | 51455 |
| rs747184995 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421124 | ACAGGAATAGCTCCA[C/T]GTGCCGGGAGGCTGA | 51455 |
| rs747207892 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99406692 | TGAGTGGTCATTCAT[A/C]TCAAACTTCAGAGTA | 51455 |
| rs747208883 | snp | C/T | 1.689e-05 | 0.00290598 | intron-variant | REV1 | GRCh38.p7 | 2:99412977 | GAATATAGTTAAGTA[C/T]GCAGAATAAGCTACT | 51455 |
| rs747215539 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99464967 | CTTCCTCCATCCACC[C/T]CGCCTCATGGTGGAG | 51455 |
| rs747236922 | snp | C/T | 0.00015294 | 0.00874338 | intron-variant | REV1 | GRCh38.p7 | 2:99408177 | TTCATTCCATATGTA[C/T]TCACTAGTACTAAAG | 51455 |
| rs747240906 | in-del | -/T | 1.99954e-05 | 0.00316185 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439327 | TAAAGCAGGAAAAAA[-/T]TTTTGAGTTAATAAT | 51455 |
| rs747253549 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99409125 | ACATAAATAAGTTTT[A/T]AAAGTAAATAAATAA | 51455 |
| rs747265607 | snp | G/T | 1.68587e-05 | 0.00290329 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402371 | GGGAAAAACTTCAAA[G/T]GAGGACCAGTCTTTT | 51455 |
| rs747273654 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442404 | AAGCTGAGACCTTTC[C/T]GCACACTGGACTGCT | 51455 |
| rs747273951 | in-del | -/AAC | | | intron-variant | REV1 | GRCh38.p7 | 2:99485132 | ACTGAGAAATGAAAT[-/AAC]AATCCTACAAAGAAG | 51455 |
| rs747296504 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486986 | AATAAAGAATAAAAG[A/T]TTATAAAGGAAGGGG | 51455 |
| rs747314259 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472265 | GCTACAACTTGCATG[A/T]ACCTTGAAGGCATTA | 51455 |
| rs747385828 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99409023 | GCTGAGCACAGTGGC[A/T]CACACCTGTAATCCC | 51455 |
| rs747413106 | in-del | -/T | 1.67483e-05 | 0.00289377 | intron-variant | REV1 | GRCh38.p7 | 2:99462675 | ACATTTTCTCCCCCC[-/T]TTTTTGAAAAAAAAA | 51455 |
| rs747424620 | snp | A/C | 0.000133286 | 0.00816243 | intron-variant | REV1 | GRCh38.p7 | 2:99449321 | TATTAATTAAATTTA[A/C]TAAATTAAACTTACC | 51455 |
| rs747488756 | snp | G/T | 4.97896e-05 | 0.00498922 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408055 | CTGATATATTTAGTT[G/T]CATTGTATGAAACAT | 51455 |
| rs747523131 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430810 | AACACAACTTCATCA[C/T]AGGTCTCTTGGGATA | 51455 |
| rs747524266 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99422684 | TTCCCAAGGGTGGTA[C/G]AAGAACACTACTGTG | 51455 |
| rs747532464 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490470 | CAGTGGGGAAGGACA[C/T]AAGTGCAGACACTGA | 51455 |
| rs747551678 | snp | C/T | 1.66043e-05 | 0.00288129 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438632 | AAGTGCAGACCTGCC[C/T]GTTTTCATTTTTTTT | 51455 |
| rs747603960 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415471 | ATCCAATACAGACAT[A/G]GAGGAGTAAACTTCA | 51455 |
| rs747645691 | in-del | -/AGTC | 0.000180099 | 0.00948773 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402397 | CTTTTTGAAGGAGAA[-/AGTC]AGAGATCTGCATGGA | 51455 |
| rs747667454 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99442160 | GGGAGGCTGAGGCAG[G/T]AGAATCACTTGAACC | 51455 |
| rs747669588 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426148 | GTCAGGAGTTGAGAC[C/T]AGCCTGGCCAACATG | 51455 |
| rs747697474 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487733 | ATTCTTGAAAAGCAG[A/G]AAGACCCACAATGCT | 51455 |
| rs747717271 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419809 | GCAGAGCTCAGCTGC[C/T]AGGTGGGCTTCTCCG | 51455 |
| rs747758051 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404521 | CTGGTATTTGCAACA[A/G]GACTGTCCCAACTGG | 51455 |
| rs747758901 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427195 | TCTGGGGGAAAAAAA[C/T]TGCCATCAAACCACT | 51455 |
| rs747769273 | snp | A/G | 1.66272e-05 | 0.00288328 | intron-variant | REV1 | GRCh38.p7 | 2:99435973 | AGCATTCAAACCCCA[A/G]GCTAATTTTTACTAT | 51455 |
| rs747771522 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462237 | TACAAGTCCTACTAC[C/T]CATGTGTGGTAATTT | 51455 |
| rs747809582 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99467901 | AAATACAAAAGATTG[A/C]TGGGCACGATGGCTC | 51455 |
| rs747843772 | snp | A/C | 6.70826e-05 | 0.0057911 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401207 | AAGCACTTATGGCAC[A/C]GCTATCAGAGAGCAT | 51455 |
| rs747880703 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448851 | ACCCCTAATTCCTGG[C/T]AAACACATTAACATG | 51455 |
| rs747881478 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99413644 | TTCTGCAAGATGTAA[A/C]GTTTGAGCCCCACCT | 51455 |
| rs747908931 | snp | A/G | 2.39026e-05 | 0.00345698 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403091 | GCCTTTAGATGAAGT[A/G]AAGGATTCTTTGGCA | 51455 |
| rs747967220 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478969 | GAATGATGCTACAAC[A/G]TGTCCTAAGTAGAAT | 51455 |
| rs747971890 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400259 | AGTAGAGATTTTTAT[A/C]CATTAATCTTGATCT | 51455 |
| rs747973449 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450474 | TAATCCCAAGCAATA[C/T]AGGTCCAAGTATTTA | 51455 |
| rs747974845 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99401358 | CTGCATCAGCCTAAA[C/G]GTGGGGAGAGAAGAA | 51455 |
| rs748001453 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99435673 | AGAAAGAAAAACTCT[A/C]ATTTCCCTATACCTT | 51455 |
| rs748033793 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477240 | AATCGGGGGTGGCCA[C/T]GTGACTAAGTTCTGG | 51455 |
| rs748058035 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460114 | TCTTTTTTTCACTCT[A/G]TCGCCAGGCTGGAGT | 51455 |
| rs748094066 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439120 | TTAAGGCACCATTAG[A/G]GCTAGGAGTGTGTCC | 51455 |
| rs748096033 | snp | C/G | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406358 | CGGTGGATTTCTTAG[C/G]TTTCTGAACTTGGAA | 51455 |
| rs748172108 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99437145 | CCACCACGCCCAGCT[A/G]ATTTTTTTTTTCTTT | 51455 |
| rs748184459 | snp | A/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403000 | GTTAAGCAGCTTGTT[A/T]TTCAAAGGACTCTGA | 51455 |
| rs748192555 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462593 | AAACTGTTCCTCCAA[A/T]TTCTGGACCTTGGCA | 51455 |
| rs748204349 | in-del | -/AT | | | intron-variant | REV1 | GRCh38.p7 | 2:99465187 | AACACCCTCCTACAC[-/AT]ATGTTTAAATTGTAA | 51455 |
| rs748232021 | snp | A/G | 1.68057e-05 | 0.00289872 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405917 | AAATGTACCTGGGAA[A/G]GTGACGGGACCTCTA | 51455 |
| rs748242202 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99471987 | ATGGTGCAGCTGATA[C/T]GAGAAACAGTATGGC | 51455 |
| rs748245113 | in-del | -/AAAAAAAC | 2.9277e-05 | 0.00382592 | intron-variant | REV1 | GRCh38.p7 | 2:99442269 | AAAAAAAAAAAAAAA[-/AAAAAAAC]AAAAAAACCAACCAG | 51455 |
| rs748262177 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99422519 | ATTAAGATCTCTATT[A/C]AAGAAATAATCTATT | 51455 |
| rs748279546 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484806 | CAAACAAAAACCTTG[C/T]CATTTTAAGGTGTCC | 51455 |
| rs748282400 | snp | A/C | 1.64855e-05 | 0.00287097 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438816 | GAAGGTGCTGCCTTG[A/C]TAAACGTAGATACTG | 51455 |
| rs748295783 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432137 | TCATCAATGAGAAGT[A/G]TGACTACTGAGTACT | 51455 |
| rs748319460 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409545 | AGTTGGCCCTGACAT[A/G]AAAGACGAGTGTTTC | 51455 |
| rs748332155 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470674 | TCCTTTGTTCTCCTC[C/T]GCCTTTGCCTCTTTT | 51455 |
| rs748351575 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99444289 | CATAGATAGCTATAA[C/G]TAAGAGACAAGTAGA | 51455 |
| rs748370195 | snp | C/G | 1.64936e-05 | 0.00287168 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434412 | CGTAAAGGTGCCCTT[C/G]CTGTGCCTCTGTTAC | 51455 |
| rs748381265 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99445368 | TGGCATGAACCAGAA[C/T]AATAAATTATCATTC | 51455 |
| rs748422540 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99446919 | CCCAGATAAAAACTC[-/T]TAGCTCTAGTGACAA | 51455 |
| rs748435976 | in-del | -/GA | 4.9534e-05 | 0.0049764 | intron-variant | REV1 | GRCh38.p7 | 2:99401364 | CAGCCTAAAGGTGGG[-/GA]GAGAAGAAATGTCAT | 51455 |
| rs748453932 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483793 | TGTAGCAGGGGGAAA[A/C]AATGGCCTTGGGGGG | 51455 |
| rs748492963 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99474624 | TGATAAGCAGAAGTC[A/G]GGAGCGATGGCTCAC | 51455 |
| rs748526494 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99406983 | GAGAAATCACAATTA[C/T]GGCTGGCTTAGTGAC | 51455 |
| rs748531051 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430970 | CAGCTATTCCAGACA[A/T]ATCTATTTTGAGTGC | 51455 |
| rs748573512 | snp | A/T | 1.65042e-05 | 0.0028726 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438878 | AACAGTGGAGTGGTG[A/T]GCACCATTGATTTTA | 51455 |
| rs748618982 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416484 | TTGGGGATTTTATGA[A/G]AACCACATGAACCAC | 51455 |
| rs748637281 | snp | A/G | 4.97368e-05 | 0.00498657 | intron-variant | REV1 | GRCh38.p7 | 2:99424132 | ACACAGACACAAAAT[A/G]ACAGTTTGATACACT | 51455 |
| rs748643696 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417657 | CAACCCTGCTGACAC[C/T]TTGATCTTGAACTTC | 51455 |
| rs748695586 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402672 | TATCCATTCTCTGAG[C/G]AAGGTCTTCACATCA | 51455 |
| rs748696275 | in-del | -/AG | | | intron-variant | REV1 | GRCh38.p7 | 2:99458732 | TTTTGATGACCTGAC[-/AG]ATAATTTATGCTCAG | 51455 |
| rs748722598 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454027 | CCTCATTGTTCTTTG[C/T]CTTTTTATTTTTTAT | 51455 |
| rs748729958 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403380 | TTTGTGATGCATTTT[A/G]AACCAACATCCTTTA | 51455 |
| rs748742669 | snp | C/T | 1.6495e-05 | 0.0028718 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435844 | CAGACCTTTGAGATC[C/T]GGTCTATTTCGTATA | 51455 |
| rs748742826 | snp | C/T | 5.97961e-05 | 0.00546758 | intron-variant | REV1 | GRCh38.p7 | 2:99449298 | AAAGTATTCTAACTT[C/T]AAAAATTTATTAATT | 51455 |
| rs748782234 | snp | C/T | 1.66983e-05 | 0.00288944 | intron-variant | REV1 | GRCh38.p7 | 2:99418792 | AAGTACTTGTAATGC[C/T]TGTAATAAAAGTATT | 51455 |
| rs748828599 | snp | C/G | 1.65015e-05 | 0.00287237 | intron-variant | REV1 | GRCh38.p7 | 2:99435945 | CTGACATATCTCCTA[C/G]AAGGAAAAAGACAGC | 51455 |
| rs748870303 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99446722 | CTGGTCTTGAACTCC[C/T]GACCTCGTGATCCAC | 51455 |
| rs748887826 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415375 | TGGGACAAAGACTTG[A/G]CATCTGTCCTTGAAG | 51455 |
| rs748900953 | snp | C/T | 1.77539e-05 | 0.00297937 | intron-variant | REV1 | GRCh38.p7 | 2:99410654 | TTACAACAACCTGTA[C/T]TGAAATATAATTACC | 51455 |
| rs748920214 | snp | A/C | 0.000131789 | 0.00811648 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403735 | AGTGCTGTTCTCGCC[A/C]TGCCTTTGTCTTTGA | 51455 |
| rs748931521 | snp | C/T | 6.26625e-05 | 0.00559708 | intron-variant | REV1 | GRCh38.p7 | 2:99403865 | GCTAATTGTAGATGG[C/T]AGCTGGTTTCTCTTT | 51455 |
| rs748935126 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442381 | CCTCAGGTCTGCATA[C/T]AGGATTAAAGCTGAG | 51455 |
| rs748936746 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486122 | AGAGCAAGACCCTGT[C/T]TCAAAAAATGTTAAA | 51455 |
| rs748951586 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477863 | GGGGGCTTCCTGAAA[C/G]AACGACTAATGCTTT | 51455 |
| rs748993833 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419640 | CGCGACTGGACTGGG[A/G]AAACCAGAAAGCCCA | 51455 |
| rs749011725 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436143 | AATTAGTCAAAAAGT[A/G]CATCTTAAAATTATT | 51455 |
| rs749039223 | in-del | -/TGAGT | | | intron-variant | REV1 | GRCh38.p7 | 2:99444974 | GGTTTCCTTATACAC[-/TGAGT]TTTTTCATGTACATT | 51455 |
| rs749048695 | snp | A/G | 1.65007e-05 | 0.00287229 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439013 | TCTGAAATCAGTGCT[A/G]CTCTTCTCAGCCTTA | 51455 |
| rs749049635 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99468180 | AGCGAAACTCCATCT[-/C]AAAAAAAAAAAAAAG | 51455 |
| rs749062324 | snp | C/T | 1.65135e-05 | 0.00287341 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439088 | GTTGACCATGGGCAC[C/T]AAGCAATCCTGTGTC | 51455 |
| rs749073739 | snp | A/G | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402794 | AAGTAGAAGCAGAGA[A/G]TTCTTCCTGTTAAGA | 51455 |
| rs749108525 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99437243 | CCGCCTCGGCCTCCG[A/C]AAGTGTGCGAATTAC | 51455 |
| rs749136581 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422926 | CCCTCGTTTGGATGC[C/T]ACCACTGACTTCCTC | 51455 |
| rs749174950 | in-del | -/CC | | | intron-variant | REV1 | GRCh38.p7 | 2:99409855 | CTCAAAACAAACAAC[-/CC]CCCCCCCCCCCAAAA | 51455 |
| rs749223358 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458309 | TGTTTCACCAATGAT[G/T]ATGTAAAGATAAGAA | 51455 |
| rs749229155 | snp | A/G | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418937 | CATTCTAGCCAGGAG[A/G]ATATTAGAACCTATT | 51455 |
| rs749285677 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99470554 | CTAAATATTTGCCCC[A/G]GCAAGCTTATACTGG | 51455 |
| rs749294432 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99424066 | CAAAAGTGATCCTGA[A/C]AATCCTAAAGAAAAC | 51455 |
| rs749303812 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99473685 | TTTTCCTGTTGCTAA[-/T]TTTTTTCTGCTGCAA | 51455 |
| rs749308313 | in-del | -/CCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99409854 | TCTCAAAACAAACAA[-/CCC]CCCCCCCCCCCAAAA | 51455 |
| rs749341649 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453027 | GTGGGAATTAAGAGC[C/T]AAAAATTATAAATTA | 51455 |
| rs749370660 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404562 | ATTCCTGTATTACAG[C/T]CATTTACTGGTTCTT | 51455 |
| rs749372697 | snp | A/G | 3.30404e-05 | 0.00406437 | intron-variant | REV1 | GRCh38.p7 | 2:99412726 | ATCTGTTCAATGATC[A/G]GTACCTGAGTAAACC | 51455 |
| rs749383192 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483667 | CCAATGATAAAATCA[A/G]GACTTTAAATCGTAA | 51455 |
| rs749390741 | in-del | -/AT | | | intron-variant | REV1 | GRCh38.p7 | 2:99429229 | TAAATTATGAGGAAG[-/AT]ATATATATATGAGTG | 51455 |
| rs749400007 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400778 | AGAATAAGATGGTTT[-/A]AGAAGCTTTACCCTT | 51455 |
| rs749406001 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99445885 | CACCCCACATACTTA[A/C]AAGTGGCAGTTCCTT | 51455 |
| rs749425702 | snp | A/C | 0.000138725 | 0.00832726 | intron-variant | REV1 | GRCh38.p7 | 2:99451511 | ACCAATCTAGTTAAA[A/C]GGCAAGATCACATAA | 51455 |
| rs749437196 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447370 | AGAGACAGGGTTTCA[C/T]CAAGTTGGCCAGGAT | 51455 |
| rs749441577 | snp | A/C | 0.000644491 | 0.0179396 | splice-acceptor-variant, missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429946 | ATGAATCTGGTATAT[A/C]TGCTTTAAAAATAAA | 51455 |
| rs749468677 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481941 | CCAACTGATAGGAGT[A/G]TCTTTGTTATCCATG | 51455 |
| rs749491910 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99431185 | ACCCATACAAGCATT[A/T]CTGGATTTCGGCAAC | 51455 |
| rs749527050 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432002 | TTTAAAACTGTTGTT[C/T]TTTAGAATGAAAACT | 51455 |
| rs749567096 | snp | C/G | 3.32502e-05 | 0.00407725 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410843 | CTTCTGAAAGACTCA[C/G]AAGAAAAGCTTCTGC | 51455 |
| rs749608176 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436990 | CCAACTTTTTTTTTG[-/T]TTTTTTTTTTTTTTT | 51455 |
| rs749640860 | in-del | -/TTC | 1.89091e-05 | 0.00307477 | cds-indel, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403063 | CTTGTTTCTTTTCTT[-/TTC]TTTCACTGCTGCCTT | 51455 |
| rs749647824 | snp | C/T | 1.66048e-05 | 0.00288134 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402341 | GAATGTCTTCTTCCA[C/T]TGGATCTAGGAAGGG | 51455 |
| rs749671687 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418018 | CGGGGGTCAGGAAGC[G/T]TTAAAACTAACCTAC | 51455 |
| rs749683092 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99476152 | CTGTGCAGTAAGAAT[A/C]CTAACCCAAACAGAT | 51455 |
| rs749688402 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461729 | AAAGATAAAACTGAA[A/G]CTGGCCATATGGAAG | 51455 |
| rs749697390 | snp | A/T | 3.32105e-05 | 0.00407482 | intron-variant | REV1 | GRCh38.p7 | 2:99424123 | AGAAGGAAAACACAG[A/T]CACAAAATGACAGTT | 51455 |
| rs749720563 | in-del | -/AATT | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401141 | TTAAAAGAAATTTAA[-/AATT]AATTATAAAAACTCC | 51455 |
| rs749725328 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99475221 | ATACTGCTGTGTCTG[A/G]TTTCCATTGGCTGGA | 51455 |
| rs749745068 | snp | G/T | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404658 | TCAGGTGGAAGTGCT[G/T]CTAAAACAGACTGAT | 51455 |
| rs749761616 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99404851 | TTTTTGGAACGTCTT[A/G]GCCTTTTGTCATTGA | 51455 |
| rs749776931 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455445 | ACAATCAACTAAAAG[C/T]CACGGATACACTCAA | 51455 |
| rs749784437 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99444064 | TGACCTCGTGATCCA[C/G]CCGCCTCTGCCTCCC | 51455 |
| rs749795049 | snp | C/T | 1.65501e-05 | 0.00287659 | intron-variant | REV1 | GRCh38.p7 | 2:99401377 | GGGAGAGAAGAAATG[C/T]CATTAGGAATTAGGA | 51455 |
| rs749804815 | snp | C/T | 1.65392e-05 | 0.00287564 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438670 | CCCTTCCTGGAAAGA[C/T]ACCATTACTTTGTCT | 51455 |
| rs749903790 | in-del | -/AAAAG | | | intron-variant | REV1 | GRCh38.p7 | 2:99468191 | ATCTCAAAAAAAAAA[-/AAAAG]AAAGAAAGAAAAATT | 51455 |
| rs749914802 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469559 | AGGCAAATGGGAGAG[C/T]AGCTCTGTCTATGAG | 51455 |
| rs749943386 | snp | C/G | 3.29641e-05 | 0.00405968 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402962 | GGACTGCCACAGGCC[C/G]CTGGCAGAGTTTTTG | 51455 |
| rs749948340 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431768 | GCAGCAGAGTGCGTG[A/G]GTCCCTCCACGAGCG | 51455 |
| rs749973933 | snp | G/T | 1.66355e-05 | 0.002884 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402632 | GGGCCATCTAACACA[G/T]GCCAAGCCAACCTGA | 51455 |
| rs749977174 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430885 | ACATTCTAAAACCAC[A/G]ACCTCAGCCACATCT | 51455 |
| rs749990549 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459862 | AAGTTCAATGTTAAC[A/T]GGGTTGGAAGGTATA | 51455 |
| rs750026851 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472708 | GTTTTTTACTTTGAA[C/T]TGGCAGTAGTGGGAG | 51455 |
| rs750034201 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417419 | ACAGTGCTGGGATTA[C/T]AGGTGTGAGTCACCA | 51455 |
| rs750078586 | snp | A/C | 3.30104e-05 | 0.00406252 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438950 | GTGTGGATTCCGCAA[A/C]GCATCTGTGTTTCTG | 51455 |
| rs750102182 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99455016 | AGGCCCAGCTTATAG[A/G]AAGTTTTGCTCATCT | 51455 |
| rs750140519 | snp | C/G | 3.29897e-05 | 0.00406125 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402790 | CCTGAAGTAGAAGCA[C/G]AGAGTTCTTCCTGTT | 51455 |
| rs750164918 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99471274 | GGTTAATAAAGGGCT[G/T]AAGGTATGATCCAAC | 51455 |
| rs750182576 | in-del | -/G | 1.65733e-05 | 0.00287861 | intron-variant | REV1 | GRCh38.p7 | 2:99401383 | GAAGAAATGTCATTA[-/G]GAATTAGGAAAGGTC | 51455 |
| rs750211082 | snp | C/G | 1.68243e-05 | 0.00290032 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401195 | CAAATACCTCACAAG[C/G]ACTTATGGCACAGCT | 51455 |
| rs750252112 | snp | C/T | 4.9458e-05 | 0.00497258 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418915 | CTGGTTTTGCTTTTC[C/T]AGTTGCCATTCTAGC | 51455 |
| rs750286134 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410765 | CCCCAGGCTTTCGTA[C/T]CATGATTTTGAGAGT | 51455 |
| rs750294103 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483390 | ATTTTAGCCTTGGGT[A/G]TGATCAGGAATGACT | 51455 |
| rs750331525 | snp | C/T | 3.31494e-05 | 0.00407107 | intron-variant | REV1 | GRCh38.p7 | 2:99442507 | TTTAGAGTTCCATAC[C/T]TGGTGACAATGAGCT | 51455 |
| rs750334456 | snp | A/C | 1.87054e-05 | 0.00305816 | intron-variant | REV1 | GRCh38.p7 | 2:99403846 | AGGTCAAAGTCAAAC[A/C]TGAGCTAATTGTAGA | 51455 |
| rs750342932 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99489140 | AACAGTACAGAAGTG[C/G]GCAAGGGGCTCTCGG | 51455 |
| rs750408551 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463553 | TCACAAAATATTGTT[C/G]TTATGTACACAATTG | 51455 |
| rs750426102 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99426877 | TTGTATTTGGTGTTG[C/G]ATTCAACAATATTAA | 51455 |
| rs750448477 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99457062 | TATGAAGTATTCACT[-/C]CCACTCCCAAAGGCA | 51455 |
| rs750448494 | in-del | -/AT | 1.66134e-05 | 0.00288208 | intron-variant | REV1 | GRCh38.p7 | 2:99404694 | TATAAAATGCCAAAC[-/AT]ATGAGTAGGAAGTTA | 51455 |
| rs750515080 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456962 | GTTGAAAATGTAGGT[C/T]AGAATTAGGACTAGA | 51455 |
| rs750515923 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406405 | TATGACCCACTAGGA[A/G]AGTGGCTTGACTGAA | 51455 |
| rs750519867 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413128 | TGCAAAATCATGCTA[G/T]TAGATGTATTTCTAG | 51455 |
| rs750520254 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428551 | AATATAAGCATGCAC[A/G]TTTGAACTTAATGCT | 51455 |
| rs750539019 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99465798 | TATACATGTGTATCA[A/G]ATGGTTACCATATGA | 51455 |
| rs750544103 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462123 | TCTAGGAAATCTGAC[A/G]CTGACACACACCCAC | 51455 |
| rs750579966 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99479018 | AATGCAATTCACCAG[A/G]TGAAGGTTTTAATTA | 51455 |
| rs750584264 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401283 | AGTTTGTTGTAAAAC[C/T]ACCTGGACATTGTCA | 51455 |
| rs750606131 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414367 | AAGTGAGATGAAGGC[A/G]TTAAGCGTGCTCGTT | 51455 |
| rs750646981 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475977 | GACAGAGTGAGACTT[C/T]GTCTCAAAAAAATAA | 51455 |
| rs750654219 | snp | A/G | 1.65034e-05 | 0.00287253 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421650 | TTCAATGTTATGAGT[A/G]TAGCTATCAACACAG | 51455 |
| rs750680386 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99400967 | CATACAGTTCTTTAT[G/T]AAACAACTGTAAACA | 51455 |
| rs750694519 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99451183 | GGGCACCAAATCCAA[C/T]GAAATCACAGAAATC | 51455 |
| rs750712049 | snp | A/T | 1.671e-05 | 0.00289045 | intron-variant | REV1 | GRCh38.p7 | 2:99406316 | AGAACCACATTGATG[A/T]CCACCAACCTTCTTT | 51455 |
| rs750732918 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99457313 | GATGTCAATTCTCCC[C/T]GAACTGATCTACAGG | 51455 |
| rs750826900 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488897 | GCCCTTGTTGTGCTA[C/T]GTGCTAGTCTGCATT | 51455 |
| rs750839029 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462546 | AAAATTGTAGATGAA[C/G]TCCCATCCTTCTGCA | 51455 |
| rs750849987 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415850 | AGAGTGCATGCGCAG[A/G]TAAAAAGCCCTGCAA | 51455 |
| rs750911057 | snp | A/C | 3.35374e-05 | 0.00409482 | intron-variant | REV1 | GRCh38.p7 | 2:99429998 | TATAAACTGATTTTC[A/C]CTCACTTTTTCAAGA | 51455 |
| rs750923647 | snp | A/G | 1.94079e-05 | 0.00311505 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439320 | TGATTTCTAAAGCAG[A/G]AAAAAATTTTTGAGT | 51455 |
| rs750925641 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468835 | TAACTACTGTTATAG[C/T]AATCTACTCTGCCAG | 51455 |
| rs750932179 | in-del | -/CCT | 1.67073e-05 | 0.00289022 | intron-variant | REV1 | GRCh38.p7 | 2:99462673 | TTACATTTTCTCCCC[-/CCT]TTTTTGAAAAAAAAA | 51455 |
| rs750998200 | snp | C/T | 3.29794e-05 | 0.00406061 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434389 | CCAGCTGGGGGTTAG[C/T]GCCAGGACGTAAAGG | 51455 |
| rs751001097 | snp | A/T | 1.65395e-05 | 0.00287567 | intron-variant | REV1 | GRCh38.p7 | 2:99412720 | GGCAAAATCTGTTCA[A/T]TGATCAGTACCTGAG | 51455 |
| rs751039020 | snp | C/T | 1.65116e-05 | 0.00287324 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438944 | AGTTCTGTGTGGATT[C/T]CGCAAAGCATCTGTG | 51455 |
| rs751109340 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419483 | CCAAAGTGCTGGGAC[G/T]ACAGGAATGAGCCAC | 51455 |
| rs751128987 | snp | C/T | 1.7795e-05 | 0.00298282 | intron-variant | REV1 | GRCh38.p7 | 2:99405887 | TATAAAATGTACTTA[C/T]ATTTAGGACTACAAA | 51455 |
| rs751177230 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456296 | ACTGGAGATATGGCA[A/T]TGAACAAGACTCAAG | 51455 |
| rs751189819 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99466249 | AGCCACCGTGCCCGG[A/C]CTCTTTTTTTTGAGA | 51455 |
| rs751223945 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant | REV1 | GRCh38.p7 | 2:99464878 | GAAGAATGAAAAATA[A/G]CTAGACAGTTCGATA | 51455 |
| rs751254046 | snp | A/T | 1.64819e-05 | 0.00287066 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442352 | GGCTATATTGCTTGG[A/T]CCTGGCAGAGGATCC | 51455 |
| rs751261313 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99402020 | CAGGCGTGAGCCACT[A/G]TGCCCAGCCCACTTC | 51455 |
| rs751273706 | snp | G/T | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405953 | AGGTTAAGTCTCGAC[G/T]GCACACTGACAGGAG | 51455 |
| rs751304421 | in-del | -/ATTAA | 3.35993e-05 | 0.0040986 | intron-variant | REV1 | GRCh38.p7 | 2:99434462 | TCCTGTGAGGAAAAT[-/ATTAA]ATTATTTCTGTATGT | 51455 |
| rs751305393 | snp | C/T | 4.59021e-05 | 0.0047905 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402285 | CAGTTTTTCCAAATC[C/T]TTTTCTTCTATTAGA | 51455 |
| rs751337675 | in-del | -/A | 4.94539e-05 | 0.00497238 | frameshift-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406021 | TTAGTATCAGGACTG[-/A]GTCGGCAGATGTGCA | 51455 |
| rs751356889 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99443228 | TACTTATGCTATCAT[C/G]CAAATTTCAAAACAA | 51455 |
| rs751382418 | in-del | -/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433283 | AACAGCTACTCCACA[-/T]CTACTCATGACACAC | 51455 |
| rs751400529 | snp | A/G | 1.65449e-05 | 0.00287614 | intron-variant | REV1 | GRCh38.p7 | 2:99442491 | CAAAAAGCAACACCA[A/G]TTTAGAGTTCCATAC | 51455 |
| rs751427991 | snp | C/T | 1.67058e-05 | 0.00289009 | intron-variant | REV1 | GRCh38.p7 | 2:99435807 | ACAATATATCAGTTT[C/T]CTTAAAACATAAGCA | 51455 |
| rs751461946 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428621 | TTTAAAAAAAACTAT[C/T]ATGATTAGACGATGC | 51455 |
| rs751527936 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463304 | GTGGGCAGATCACCT[C/G]AGGTCAGGAGTTCGA | 51455 |
| rs751606478 | in-del | -/TCTTTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99451079 | ATCTACAGTTCAGTT[-/TCTTTC]TCTAACACTAAAGAA | 51455 |
| rs751671000 | snp | A/C | | | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406482 | CAACTGATTCACGTG[A/C]ATCCCAACCTAGAAC | 51455 |
| rs751677832 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401073 | ACACAATTATTTACA[C/T]GCAATACTGACAAAT | 51455 |
| rs751706685 | snp | C/T | 1.69833e-05 | 0.00291399 | intron-variant | REV1 | GRCh38.p7 | 2:99421449 | AAATTAACTGATATT[C/T]AAGAATCTCAAAGCA | 51455 |
| rs751763711 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99402240 | AAAAGTGATGAATTA[C/T]TACCTTTTCATGTAT | 51455 |
| rs751802822 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488755 | TAGAAAGAACCAAGG[C/T]TATGGTTGGTCCTAC | 51455 |
| rs751806885 | snp | C/T | 3.29739e-05 | 0.00406028 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435908 | TGCATTATACAGCTC[C/T]GATGTCTGGGAGAAT | 51455 |
| rs751860453 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468774 | GAATACATGAATGCA[A/G]AAGTACCCTTACCCT | 51455 |
| rs751869043 | in-del | -/TT | 0.000148342 | 0.00861099 | intron-variant | REV1 | GRCh38.p7 | 2:99403655 | GTGACTCCATTACTC[-/TT]TGTCTTCATTTTTGT | 51455 |
| rs751872214 | snp | A/C/T | 8.31851e-05 | 0.00644878 | intron-variant | REV1 | GRCh38.p7 | 2:99429982 | ATTAATGGTTATATG[A/C/T]TATAAACTGATTTTC | 51455 |
| rs751893942 | snp | A/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418866 | CCTCTGATAAAATCA[A/T]CTACTTCTTCTGGTT | 51455 |
| rs751915540 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99423653 | TTCTCAAGCCAACTC[A/G]TCAACCATTTTGAAA | 51455 |
| rs751929744 | in-del | -/AAGA | | | intron-variant | REV1 | GRCh38.p7 | 2:99478653 | AACAGAACTTAGCTG[-/AAGA]ATAAAGGAAATAATA | 51455 |
| rs751951931 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410254 | GGCCTCAAGTGATCC[A/T]GCTGCCTCAGCCTCC | 51455 |
| rs751961641 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99413363 | TGTAAGGGATCTATT[A/G]TGATTTCGGTCATCA | 51455 |
| rs751972559 | snp | C/G | 1.65195e-05 | 0.00287393 | intron-variant | REV1 | GRCh38.p7 | 2:99402828 | CAAAGGATAAAATTG[C/G]TATATTCACACATTA | 51455 |
| rs751994426 | in-del | -/GATGGA | | | intron-variant | REV1 | GRCh38.p7 | 2:99421034 | TTTAAAGACAGCATG[-/GATGGA]GATGGAGATGGAGGA | 51455 |
| rs752038690 | snp | A/T | | | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479782 | CCAAAAAAGTAAAAA[A/T]AATAATAATAATAAT | 51455 |
| rs752045307 | in-del | -/ACTA | | | intron-variant | REV1 | GRCh38.p7 | 2:99417974 | TTACACATTTCTGAC[-/ACTA]ATACATCGTTTTAAG | 51455 |
| rs752074020 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99445121 | GTCCTACAGCCTCTG[C/T]GTTTAGGAACAAAAA | 51455 |
| rs752074358 | in-del | -/CTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99445760 | TTTAATGTACACAGG[-/CTC]CTCATGAAAGGATTC | 51455 |
| rs752114444 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439173 | CTGGGATGCGGAATT[C/T]CATTCTGTTTCCTTC | 51455 |
| rs752125775 | snp | C/T | 4.95389e-05 | 0.00497664 | intron-variant | REV1 | GRCh38.p7 | 2:99465010 | GGAGGAAAAAAAAAA[C/T]GTCAATTTTATAACA | 51455 |
| rs752164987 | snp | C/T | 1.66355e-05 | 0.002884 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429918 | TGCGCAGAATCTGGA[C/T]TCTCCCACAATGATG | 51455 |
| rs752172812 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468932 | CATCATTATTTTAAG[A/T]CAGTTATCCATGGTC | 51455 |
| rs752187688 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469892 | TCTGGGGGGCCGAGG[C/T]GGGCAGATCACGAGG | 51455 |
| rs752190451 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447163 | TGTTATTTATTTGAC[-/T]TTTTTTTTTTTTTAG | 51455 |
| rs752195637 | in-del | -/AA | 1.75349e-05 | 0.00296094 | intron-variant | REV1 | GRCh38.p7 | 2:99407995 | AGAGATACATTACAC[-/AA]AGTCAGAATTTACAA | 51455 |
| rs752243571 | snp | A/G | 1.65045e-05 | 0.00287263 | intron-variant | REV1 | GRCh38.p7 | 2:99401359 | TGCATCAGCCTAAAG[A/G]TGGGGAGAGAAGAAA | 51455 |
| rs752243849 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421872 | AAATACAGCATATTG[G/T]ATAGGAAAATGTTTG | 51455 |
| rs752245509 | snp | A/G | 1.88379e-05 | 0.00306897 | intron-variant | REV1 | GRCh38.p7 | 2:99405871 | TATTTATATTTAGGA[A/G]TATAAAATGTACTTA | 51455 |
| rs752246168 | snp | A/G | 7.14056e-05 | 0.00597476 | intron-variant | REV1 | GRCh38.p7 | 2:99410913 | ATTCCACTTTCCTAT[A/G]TACCTAATAATTGTT | 51455 |
| rs752278319 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482491 | GAGTTTGTAGCTAAT[A/G]TAAGAAGTGAGGAGA | 51455 |
| rs752283493 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438779 | TGAAATAAAATTGCA[A/G]TCTGAAGGTTTGGAT | 51455 |
| rs752284924 | snp | G/T | 2.3491e-05 | 0.00342709 | intron-variant | REV1 | GRCh38.p7 | 2:99449544 | TTAAGAGTCTTATGT[G/T]TAAGAAGTAGAACCC | 51455 |
| rs752333762 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99408823 | CTACCAGTTCTCTTT[A/C]CAAAGGAAAGTTATT | 51455 |
| rs752360794 | in-del | -/TTC | 3.57436e-05 | 0.00422736 | intron-variant | REV1 | GRCh38.p7 | 2:99438569 | ATCAAGCATGACTGT[-/TTC]TTAAGAAGACAATTT | 51455 |
| rs752367280 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491602 | AATTTTAACAGACTC[A/G]CGACCAGTTGCCGAC | 51455 |
| rs752438764 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412778 | CTGAAACAGATTTTC[C/T]TTCCTTTTCAGTTCG | 51455 |
| rs752441967 | snp | A/C/G | 3.29512e-05 | 0.00405891 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404624 | GACAGCACAGACTTG[A/C/G]TCTACTTGTTCCCGG | 51455 |
| rs752445637 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99466144 | TTTTAGTAGAGACGG[C/T]GTTTCACCATGTGAG | 51455 |
| rs752505000 | snp | C/G | 1.64798e-05 | 0.00287047 | intron-variant | REV1 | GRCh38.p7 | 2:99407979 | GCAAGCCTCAAAAAT[C/G]AGAGATACATTACAC | 51455 |
| rs752522948 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461319 | AATGATTGTGTCCAG[A/T]CACTGTAGAGGCACT | 51455 |
| rs752550840 | snp | C/T | 9.89593e-05 | 0.00703348 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438841 | ATACTGAAGAAGTGC[C/T]TTTTGTGCTTGAAGG | 51455 |
| rs752560506 | snp | A/T | 4.79996e-05 | 0.00489872 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439352 | AATAATATCTGACTT[A/T]TAGGTTAAAACAATT | 51455 |
| rs752573642 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99442253 | GCAAAACTCCATCTC[-/AAAAAAAAAAAAAAAAAA]AAAAAACCAACCAGC | 51455 |
| rs752606911 | snp | A/C | 1.66674e-05 | 0.00288676 | intron-variant | REV1 | GRCh38.p7 | 2:99421680 | GAGCAAAGGCAACGA[A/C]TCACAGCCACAGCCA | 51455 |
| rs752617590 | snp | A/G | 6.50343e-05 | 0.00570201 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402252 | TTACTACCTTTTCAT[A/G]TATTTTATAACTAGA | 51455 |
| rs752646480 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99451505 | ATGAAAACCAATCTA[C/G]TTAAAAGGCAAGATC | 51455 |
| rs752648700 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488370 | GAGCAATTCCCATCT[G/T]TACAAAAAAAATTAA | 51455 |
| rs752695111 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424234 | GAAGATTAGGACATA[A/G]TTGTTTAGCATGCCC | 51455 |
| rs752699126 | snp | A/G | 1.67542e-05 | 0.00289427 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406435 | ACTGATGGGCGACTG[A/G]GACATGTGGAAGGGT | 51455 |
| rs752701151 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472926 | CAGCTGTTTGTGGGT[A/T]TTGTTTTGATTCAAC | 51455 |
| rs752738066 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453108 | GCTCACACCTGTAAT[C/T]CCAGCACTCTGGGAG | 51455 |
| rs752742712 | in-del | -/TA | 1.67959e-05 | 0.00289787 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401199 | TACCTCACAAGCACT[-/TA]TGGCACAGCTATCAG | 51455 |
| rs752811165 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418856 | CACTAGCTGGCCTCT[A/G]ATAAAATCATCTACT | 51455 |
| rs752812634 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99423889 | GAACCACAGACTAGA[A/G]GTAATATAAGCAAAT | 51455 |
| rs752834611 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99485288 | AGTCACTGTCTCCAT[A/C]AATTCTTTCTTCTCT | 51455 |
| rs752835496 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486796 | CTGACAGCCTACTAT[A/G]TACCAGGCACAGTTC | 51455 |
| rs752914454 | snp | C/G | 1.68326e-05 | 0.00290104 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403808 | GCAGCAAATACCTCA[C/G]GGTCCACCTAGTGGA | 51455 |
| rs752914979 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439933 | ACTGACTATATTGAT[C/T]AACCTATTAATGAGC | 51455 |
| rs752929205 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403699 | CCAAGGCTCACCAGA[C/T]GCGCTGGCTGACTGC | 51455 |
| rs752932708 | snp | A/C | 1.64819e-05 | 0.00287066 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442341 | TTGAGCTGTTTGGCT[A/C]TATTGCTTGGACCTG | 51455 |
| rs752939266 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99465658 | ATTCATAAAAAGAGG[A/C]TAAATGAAACCCCTT | 51455 |
| rs752944773 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461531 | CTGAAAGATAGCAGG[-/T]TATCAGCCAGCTGAG | 51455 |
| rs752951794 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99467159 | GATCCAGTTGTGTAA[C/T]GTCTGTTGTATACCT | 51455 |
| rs752954644 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410502 | AACCAACCTCCTGTG[C/T]GTGGGCCTCGCTGAA | 51455 |
| rs752966946 | in-del | -/GG | | | intron-variant | REV1 | GRCh38.p7 | 2:99476319 | CCCAACACTTTAGGA[-/GG]GGCTGAGGCGGGCAG | 51455 |
| rs753024395 | snp | A/C/G | 5.22037e-05 | 0.00510878 | intron-variant | REV1 | GRCh38.p7 | 2:99435797 | TATATTTATAACAAT[A/C/G]TATCAGTTTTCTTAA | 51455 |
| rs753033037 | snp | C/G | 3.30087e-05 | 0.00406242 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439053 | TGGGAAAAGGCTGGA[C/G]AAAGCCTGCTGGCAA | 51455 |
| rs753057968 | in-del | -/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491472 | TATTTTTAGTAGAGA[-/G]GGGGGTTTCACCATG | 51455 |
| rs753108954 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475931 | GAGGTTGCAGCAAGC[A/T]GAGATCATGCCACTG | 51455 |
| rs753145296 | in-del | -/AT | | | intron-variant | REV1 | GRCh38.p7 | 2:99429230 | AATTATGAGGAAGAT[-/AT]ATATATATATGAGTG | 51455 |
| rs753168709 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436843 | TCTCATAAAGGAGTT[C/T]TTCTCAGGCTTAAAA | 51455 |
| rs753172026 | snp | C/G | | | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410775 | TCGTACCATGATTTT[C/G]AGAGTTAGACGTTTA | 51455 |
| rs753197177 | snp | C/T | 4.9525e-05 | 0.00497595 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418836 | TATTTACCTGGTAGA[C/T]TGGTCACTAGCTGGC | 51455 |
| rs753217572 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477389 | AAGGACAATACCCTA[C/T]GGAAGGGCTAAGCAC | 51455 |
| rs753275542 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467681 | AACCCTATGAGTAAC[A/G]AGAAATTGGAAGTAG | 51455 |
| rs753285511 | in-del | -/A | 1.65146e-05 | 0.0028735 | intron-variant | REV1 | GRCh38.p7 | 2:99462467 | ATAAAAATACATGCC[-/A]AAATAGGGTTAAGTA | 51455 |
| rs753289072 | snp | A/C | 1.70272e-05 | 0.00291776 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406085 | GCAGATGATATTTCC[A/C]GATCCACAGCAGCCC | 51455 |
| rs753302356 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433191 | AAAAAGAAAAACCAA[A/C]CTACCACAAAAACCA | 51455 |
| rs753307508 | snp | C/T | 0.000164987 | 0.00908108 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438977 | TCTGGTGCTTTGCTG[C/T]AACTGCTGCAGAGTG | 51455 |
| rs753318319 | in-del | -/AAC | | | intron-variant | REV1 | GRCh38.p7 | 2:99465874 | GAGAATTTTTTACTT[-/AAC]AACACCTTAAACCAT | 51455 |
| rs753319945 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481001 | AAGTGACAATCTGAA[A/G]TAAGATTAGGCATAA | 51455 |
| rs753376232 | in-del | -/GAA | 0.000214343 | 0.0103501 | cds-indel, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438831 | CTAAACGTAGATACT[-/GAA]GAAGTGCTTTTTGTG | 51455 |
| rs753380213 | snp | C/T | 1.66891e-05 | 0.00288864 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449496 | TTCTCAATTCCTCAG[C/T]GGAAGGATCTGCAAA | 51455 |
| rs753389247 | in-del | -/TAAAC | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400482 | ACTAGCATAGAATTT[-/TAAAC]TAAACTATTTTTATT | 51455 |
| rs753403751 | snp | C/G | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404508 | GATTCTTGAGGTTCT[C/G]GTATTTGCAACAAGA | 51455 |
| rs753414220 | snp | C/T | 1.74836e-05 | 0.0029566 | intron-variant | REV1 | GRCh38.p7 | 2:99410902 | GAGAAACTACCATTC[C/T]ACTTTCCTATATACC | 51455 |
| rs753425330 | snp | C/T | 3.30087e-05 | 0.00406242 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402933 | GTTTTAGAAACCCAT[C/T]AATTAACTTCTGGGG | 51455 |
| rs753461178 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99473208 | TGTCTCCAAAAATCC[-/A]AAAAAAAATATTAGC | 51455 |
| rs753491251 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400205 | ACAGTAGAGATTTTT[-/A]TACATTAATCTTGAT | 51455 |
| rs753531466 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416081 | TGTGCGCAGCACGTA[C/T]GTGGTCACTAAACAT | 51455 |
| rs753566466 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99474355 | TTGTGGTACAAAATC[A/G]TACTCATCTTCTACA | 51455 |
| rs753591405 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491346 | CTGGAGTGCAATGGC[A/G]CGATCTCGGCTCACT | 51455 |
| rs753606862 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99459871 | GTTAACTGGGTTGGA[A/C]GGTATAGGGACTACG | 51455 |
| rs753612679 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410773 | TTTCGTACCATGATT[C/T]TGAGAGTTAGACGTT | 51455 |
| rs753678631 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404607 | TGTGACTCTGCTTGC[C/T]GGACAGCACAGACTT | 51455 |
| rs753681467 | snp | C/T | 0.000116396 | 0.00762788 | intron-variant | REV1 | GRCh38.p7 | 2:99421677 | ACAGAGCAAAGGCAA[C/T]GAATCACAGCCACAG | 51455 |
| rs753728083 | snp | A/G | | | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421629 | CGCTTCATCACAACT[A/G]ACAGCTTCAATGTTA | 51455 |
| rs753749814 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99471651 | AAATATCTGCAAATC[A/G]TATCTGATAAGGGGT | 51455 |
| rs753755586 | snp | A/C | 1.67823e-05 | 0.0028967 | splice-donor-variant | REV1 | GRCh38.p7 | 2:99438599 | TTTTAATAAGTATCT[A/C]CCTGTGTCAGTTACA | 51455 |
| rs753755814 | snp | A/G | 3.29761e-05 | 0.00406041 | intron-variant | REV1 | GRCh38.p7 | 2:99462484 | AATAGGGTTAAGTAA[A/G]AAGTACTCAACCTGT | 51455 |
| rs753772487 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401317 | ATAAAGTCAAATGCC[A/G]TATTCCAAACCGATT | 51455 |
| rs753785692 | snp | A/C/G | 1.6476e-05 | 0.00287014 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438742 | TTGATATGTGATGCA[A/C/G]TCTTGAATGAGAATA | 51455 |
| rs753796749 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405487 | AGCAGTATATCACAT[A/G]TACAGCCCACACACG | 51455 |
| rs753837719 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484620 | AAACATTAATTACGA[C/T]GCAAGTCATCATCCT | 51455 |
| rs753841425 | snp | C/T | 4.94271e-05 | 0.00497102 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438743 | TGATATGTGATGCAG[C/T]CTTGAATGAGAATAG | 51455 |
| rs753869271 | snp | A/C/G | 0.000131926 | 0.00812083 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434404 | CGCCAGGACGTAAAG[A/C/G]TGCCCTTCCTGTGCC | 51455 |
| rs753955948 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant | REV1 | GRCh38.p7 | 2:99403681 | TTTTGTTACATGCCA[C/T]TTCCAAGGCTCACCA | 51455 |
| rs754005416 | snp | C/T | 6.59424e-05 | 0.00574168 | intron-variant | REV1 | GRCh38.p7 | 2:99464889 | AATAACTAGACAGTT[C/T]GATATAATTATTTTT | 51455 |
| rs754043439 | snp | C/G | 3.30628e-05 | 0.00406575 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406418 | GAAAGTGGCTTGACT[C/G]AACTGATGGGCGACT | 51455 |
| rs754048000 | snp | A/G | 4.4608e-05 | 0.0047225 | intron-variant | REV1 | GRCh38.p7 | 2:99406529 | GCTTCTAGGAAAACT[A/G]AAGTGAAAATATGAA | 51455 |
| rs754058768 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426762 | CCCATACAGGATAAA[C/T]TACCAAAACTTCGTT | 51455 |
| rs754063975 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439230 | AAACTAAAATCATTA[C/T]TTTCATCTTCTTCAT | 51455 |
| rs754078568 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477355 | AGTTGTGAGGTAACC[C/T]AGCTTCAACCATGGG | 51455 |
| rs754080832 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461125 | AGTTACAAGCTTTCT[A/G]CATGTGAACTTCCCA | 51455 |
| rs754095416 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463812 | TATTTTTAATAGAGA[C/T]GGGATTTCACCATGT | 51455 |
| rs754125327 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99412694 | ATGTAAAAATATAAA[C/G]AGCAACAGATGGCAA | 51455 |
| rs754147279 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99486374 | CTCTACTAAAAATAC[-/A]AAAAATTAGCCGGGC | 51455 |
| rs754154906 | snp | C/T | 1.99035e-05 | 0.00315457 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403069 | TCTTTTCTTTTCTTT[C/T]ACTGCTGCCTTTAGA | 51455 |
| rs754158237 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99449048 | GCACTTTGGGAGGCC[A/G]AGGCTGGAGGACTGT | 51455 |
| rs754174133 | snp | A/G | 3.29728e-05 | 0.00406021 | intron-variant | REV1 | GRCh38.p7 | 2:99464890 | ATAACTAGACAGTTC[A/G]ATATAATTATTTTTA | 51455 |
| rs754233542 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433554 | CCCAACGTTTTATAA[C/T]TGACAAGGGCACTGA | 51455 |
| rs754248506 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434835 | TAGAGTTAACATCTA[C/T]ACTTATCTCTCAATT | 51455 |
| rs754289706 | snp | G/T | 3.30011e-05 | 0.00406195 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438862 | TGCTTGAAGGCCCCT[G/T]AACAGTGGAGTGGTG | 51455 |
| rs754292412 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412802 | CAGTTCGAACTGGTC[C/T]ATCATCCAAGCCACG | 51455 |
| rs754323504 | snp | C/T | 5.14126e-05 | 0.00506988 | intron-variant | REV1 | GRCh38.p7 | 2:99434498 | GTACAGGAATGTTAA[C/T]AACATGTAAGCAAAA | 51455 |
| rs754356585 | in-del | -/CTT | 0.000701995 | 0.0187218 | intron-variant | REV1 | GRCh38.p7 | 2:99462674 | TACATTTTCTCCCCC[-/CTT]TTTTGAAAAAAAAAA | 51455 |
| rs754364040 | snp | C/G | | | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406038 | TCGGCAGATGTGCAG[C/G]AAAAGGTGGCAAGAA | 51455 |
| rs754382318 | snp | G/T | 6.86742e-05 | 0.00585939 | intron-variant | REV1 | GRCh38.p7 | 2:99405905 | TTAGGACTACAAAAA[G/T]GTACCTGGGAAGGTG | 51455 |
| rs754399591 | snp | A/G | 3.3552e-05 | 0.00409571 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449497 | TCTCAATTCCTCAGC[A/G]GAAGGATCTGCAAAA | 51455 |
| rs754428066 | in-del | -/TAC | 7.42088e-05 | 0.00609088 | intron-variant | REV1 | GRCh38.p7 | 2:99402238 | ATAAAAGTGATGAAT[-/TAC]TACCTTTTCATGTAT | 51455 |
| rs754435511 | snp | C/T | 1.65965e-05 | 0.00288062 | intron-variant | REV1 | GRCh38.p7 | 2:99435968 | AAGACAGCATTCAAA[C/T]CCCAAGCTAATTTTT | 51455 |
| rs754436148 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481115 | GCAATTAAGTTACTG[A/C]AACATTTTACAACCC | 51455 |
| rs754471682 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404510 | TTCTTGAGGTTCTGG[C/T]ATTTGCAACAAGACT | 51455 |
| rs754473039 | snp | C/T | 3.35892e-05 | 0.00409798 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401204 | CACAAGCACTTATGG[C/T]ACAGCTATCAGAGAG | 51455 |
| rs754523853 | snp | A/C | 1.66189e-05 | 0.00288256 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438625 | TTACAACAAGTGCAG[A/C]CCTGCCTGTTTTCAT | 51455 |
| rs754560583 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99489430 | CGAGGCGCCGGCGCA[C/G]GAGGAAGGAGTTTGC | 51455 |
| rs754598738 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480033 | CATAATTAAAAACAT[A/C]AAAGGGCCGAGTGCA | 51455 |
| rs754602290 | in-del | -/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481399 | TATCAATAAAAAAAA[-/T]GTTATGTAGTAATTC | 51455 |
| rs754621490 | in-del | -/CCCACTAGG | 1.64863e-05 | 0.00287104 | cds-indel, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406395 | ACGGACAGAGTATGA[-/CCCACTAGG]AAAGTGGCTTGACTG | 51455 |
| rs754633938 | snp | A/C | 5.81683e-05 | 0.00539266 | intron-variant | REV1 | GRCh38.p7 | 2:99449301 | GTATTCTAACTTTAA[A/C]AATTTATTAATTAAA | 51455 |
| rs754665728 | snp | A/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410780 | CCATGATTTTGAGAG[A/T]TAGACGTTTACCCTT | 51455 |
| rs754674115 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421690 | AACGAATCACAGCCA[C/T]AGCCACCATCTGGTA | 51455 |
| rs754690399 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99479327 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 51455 |
| rs754699323 | in-del | -/CTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99446854 | GCTTTCCCCTCAACT[-/CTC]CTCCTGTCCACAGAA | 51455 |
| rs754727092 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419695 | GAAGAGTCCTCAAAA[C/T]ACAGAGACAGGCAGT | 51455 |
| rs754728085 | snp | A/G | 6.6507e-05 | 0.0057662 | intron-variant | REV1 | GRCh38.p7 | 2:99421678 | CAGAGCAAAGGCAAC[A/G]AATCACAGCCACAGC | 51455 |
| rs754728662 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99459879 | GGTTGGAAGGTATAG[A/G]GACTACGAAATCATG | 51455 |
| rs754735622 | snp | A/T | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406346 | TGTGCTCCTCTTCGG[A/T]GGATTTCTTAGCTTT | 51455 |
| rs754779533 | snp | A/G | 1.66488e-05 | 0.00288515 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406430 | ACTGAACTGATGGGC[A/G]ACTGGGACATGTGGA | 51455 |
| rs754791709 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491477 | TTTAGTAGAGAGGGG[A/G]TTTCACCATGTTGGC | 51455 |
| rs754796280 | snp | G/T | 1.65176e-05 | 0.00287376 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439252 | CTTCTTCATTCCAAC[G/T]GTTCATGCCATTGAC | 51455 |
| rs754832047 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413370 | GATCTATTATGATTT[C/T]GGTCATCACCAAATC | 51455 |
| rs754854760 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472812 | GCCCTAAAAAAAGTT[A/T]GGTAACAGTCTGCTC | 51455 |
| rs754866016 | in-del | -/TA | | | intron-variant | REV1 | GRCh38.p7 | 2:99414891 | CATAGTTTAAAATTT[-/TA]GAGTATCTTGAGTAT | 51455 |
| rs754870830 | in-del | -/ACTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99468482 | CTCTTGACTAAACCT[-/ACTC]ACTAAGAAGTGACTG | 51455 |
| rs754895961 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421541 | TCTGGTCTTTGATTT[C/G]CATACGAACAGCATT | 51455 |
| rs754921264 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438756 | AGTCTTGAATGAGAA[C/T]AGAAGTTTGAAATAA | 51455 |
| rs754941490 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486632 | ACAGTCATCCTACAG[A/G]TGAGCAGAACTGAGG | 51455 |
| rs754958373 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99435379 | TGTCCAGACGACTTA[A/G]CACATTTTAGCAATA | 51455 |
| rs755014853 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455252 | ATCTTCATTATTTCA[-/T]TTTGAGTTTCACAAT | 51455 |
| rs755029031 | snp | C/T | 1.64762e-05 | 0.00287016 | intron-variant | REV1 | GRCh38.p7 | 2:99403692 | GCCACTTCCAAGGCT[C/T]ACCAGATGCGCTGGC | 51455 |
| rs755030155 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99474370 | ATACTCATCTTCTAC[-/A]AAATTATGTTCCCAA | 51455 |
| rs755045750 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99402035 | GTGCCCAGCCCACTT[-/C]CTATGGTTTTTTAAT | 51455 |
| rs755088521 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416154 | TACCACTGAATTTCT[C/T]CTGGTTATGGTTAGA | 51455 |
| rs755095527 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459867 | CAATGTTAACTGGGT[A/T]GGAAGGTATAGGGAC | 51455 |
| rs755098985 | snp | C/T | 3.2956e-05 | 0.00405918 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412804 | GTTCGAACTGGTCTA[C/T]CATCCAAGCCACGGC | 51455 |
| rs755119274 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437134 | GCAGGTGCGTGCCAC[C/T]ACGCCCAGCTAATTT | 51455 |
| rs755120066 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99472305 | AAATAAACCATTCAC[-/A]AAAAGACAAATACTG | 51455 |
| rs755120481 | snp | C/T | | | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402426 | ATGGATAAAGGAAAA[C/T]TGCATTTCTACAACT | 51455 |
| rs755172634 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422400 | AACTTTCCCAAGAGG[C/T]CTCAGGATCAAAACT | 51455 |
| rs755184253 | in-del | -/AAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99416913 | GCAAGACTCCATCTC[-/AAAAAAA]AAAAAAAAAAAAAAG | 51455 |
| rs755188248 | in-del | -/TTC | 1.64784e-05 | 0.00287035 | cds-indel, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99464943 | TTCCCAGCCATCATT[-/TTC]AGCTCGCTTCCTCCA | 51455 |
| rs755215291 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428933 | GGAGGTGGAGCTTGC[A/G]GTGAGCCAAGATGGT | 51455 |
| rs755236723 | snp | C/G | 9.03628e-05 | 0.0067211 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402354 | CATTGGATCTAGGAA[C/G]GGGGAAAAACTTCAA | 51455 |
| rs755241916 | snp | A/G | 2.14516e-05 | 0.00327496 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439340 | AATTTTTGAGTTAAT[A/G]ATATCTGACTTTTAG | 51455 |
| rs755251673 | in-del | -/AT | | | intron-variant | REV1 | GRCh38.p7 | 2:99473962 | TGTTCCTTTTCAAAA[-/AT]AGTTTTTCTTGCTCT | 51455 |
| rs755268536 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99423713 | CTAACTTTTGGCATA[G/T]CCAATGATTTTAAGA | 51455 |
| rs755270359 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458557 | AAGATGTAACTATTA[C/T]GGGAACCAACAACTG | 51455 |
| rs755270600 | snp | C/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405975 | TGACAGGAGTATGTA[C/G]ACCATTCCATTTCCC | 51455 |
| rs755294241 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463916 | GGTGTGAGCCACCAC[A/G]CCCAACCTCAGAGCA | 51455 |
| rs755314803 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99485130 | AGACTGAGAAATGAA[A/G]TAACAATCCTACAAA | 51455 |
| rs755349559 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438864 | CTTGAAGGCCCCTGA[A/G]CAGTGGAGTGGTGAG | 51455 |
| rs755356919 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99410317 | CACCTGGCCTGTATC[A/C]TTGTTTTTAAGAACT | 51455 |
| rs755360311 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477365 | TAACCCAGCTTCAAC[C/T]ATGGGAATAAGGACA | 51455 |
| rs755394967 | snp | A/C | 3.31011e-05 | 0.0040681 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402647 | GGCCAAGCCAACCTG[A/C]AATTGTAGTTATCCA | 51455 |
| rs755435304 | snp | A/C | 1.65023e-05 | 0.00287244 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438969 | TCTGTGTTTCTGGTG[A/C]TTTGCTGCAACTGCT | 51455 |
| rs755436677 | snp | C/T | 6.61015e-05 | 0.0057486 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412934 | ATGCCAACTTAGATT[C/T]CATTGAATGTCCAAC | 51455 |
| rs755437310 | snp | A/G | 1.65452e-05 | 0.00287616 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424274 | TCCGTTCTTAATGCC[A/G]AGTTGCCTAGAGCGA | 51455 |
| rs755439063 | in-del | -/GTATTCT | | | intron-variant | REV1 | GRCh38.p7 | 2:99441123 | GAAAGCTAAAGCTAC[-/GTATTCT]GTATTCTGTGAAAAG | 51455 |
| rs755463612 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491358 | GGCGCGATCTCGGCT[C/G]ACTGCAACCTCCGCC | 51455 |
| rs755470756 | snp | A/G | 1.71319e-05 | 0.00292672 | intron-variant | REV1 | GRCh38.p7 | 2:99405906 | TAGGACTACAAAAAT[A/G]TACCTGGGAAGGTGA | 51455 |
| rs755471945 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99408441 | GCTAACATATGCACA[A/G]ATAAATACATATTTT | 51455 |
| rs755488146 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99457480 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 51455 |
| rs755568788 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99442200 | GAGGTTGCAATGAGC[C/T]GAGATCATACCATTG | 51455 |
| rs755591066 | in-del | -/T | 1.70676e-05 | 0.00292122 | intron-variant | REV1 | GRCh38.p7 | 2:99438583 | TTCTTAAGAAGACAA[-/T]TTTTAATAAGTATCT | 51455 |
| rs755601057 | snp | C/T | 7.76774e-05 | 0.00623159 | intron-variant | REV1 | GRCh38.p7 | 2:99403855 | TCAAACCTGAGCTAA[C/T]TGTAGATGGTAGCTG | 51455 |
| rs755601313 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442371 | GGCAGAGGATCCTCA[A/G]GTCTGCATACAGGAT | 51455 |
| rs755607367 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478650 | AAGAACAGAACTTAG[C/G]TGAAGAATAAAGGAA | 51455 |
| rs755617527 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443553 | AAAAACGGAACTATA[C/T]ATGATACAGAGTATG | 51455 |
| rs755639412 | in-del | -/T | 1.73833e-05 | 0.00294811 | intron-variant | REV1 | GRCh38.p7 | 2:99408012 | AGTCAGAATTTACAA[-/T]GTTACTATATACTTA | 51455 |
| rs755671617 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410766 | CCCAGGCTTTCGTAC[C/T]ATGATTTTGAGAGTT | 51455 |
| rs755709347 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99469582 | TCTATGAGGAGCCCA[A/G]GGATCCTGAATGCCT | 51455 |
| rs755747308 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99459863 | AGTTCAATGTTAACT[A/G]GGTTGGAAGGTATAG | 51455 |
| rs755781857 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99448061 | AGTTTGGAAGTTCTG[-/A]AAGCCAAGTATGTCT | 51455 |
| rs755785486 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99459207 | AGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAGA | 51455 |
| rs755793656 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99446384 | AAGATAAAATCCATT[-/A]AAGTGAATTTTAACT | 51455 |
| rs755825481 | snp | A/C | 1.69072e-05 | 0.00290746 | intron-variant | REV1 | GRCh38.p7 | 2:99438592 | AAGACAATTTTAATA[A/C]GTATCTACCTGTGTC | 51455 |
| rs755836387 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415252 | AGTAAGGGGGGCTCC[A/G]GGCCCAAAGAGTGCA | 51455 |
| rs755838583 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430564 | AGGTAATTGTATTTT[A/G]GTTTAATAATGCATG | 51455 |
| rs755853754 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99471398 | CACATGCAAAAGAAG[C/T]TGGACCTTTACACCA | 51455 |
| rs755871355 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472913 | AGATATAAAAATACA[G/T]CTGTTTGTGGGTTTT | 51455 |
| rs755915219 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99485743 | TTAATTTGCTCTAGA[C/T]ATCCACAAAATGTAT | 51455 |
| rs755945616 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419431 | TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCA | 51455 |
| rs755970680 | snp | C/T | | | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402681 | TCTGAGCAAGGTCTT[C/T]ACATCATTGAATTCA | 51455 |
| rs756020313 | snp | A/G | 4.93742e-05 | 0.00496837 | intron-variant | REV1 | GRCh38.p7 | 2:99406132 | AAAATATATAAAATA[A/G]CCTCTTCAGATCATC | 51455 |
| rs756073884 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483487 | CAACTTTTTTTGCCC[A/G]TCACTACCTAATATT | 51455 |
| rs756100486 | snp | C/T | 3.36044e-05 | 0.00409891 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401197 | AATACCTCACAAGCA[C/T]TTATGGCACAGCTAT | 51455 |
| rs756155172 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411529 | CTCCTTCCTCAGCCT[C/G]CCGAGTAGCTAGGAT | 51455 |
| rs756160847 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438652 | TCATTTTTTTTAACT[C/T]TTCCCTTCCTGGAAA | 51455 |
| rs756173127 | snp | A/G | 1.65045e-05 | 0.00287263 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439220 | CAGATCCACAAAACT[A/G]AAATCATTATTTTCA | 51455 |
| rs756231368 | snp | C/T | 3.4747e-05 | 0.00416801 | intron-variant | REV1 | GRCh38.p7 | 2:99429999 | ATAAACTGATTTTCC[C/T]TCACTTTTTCAAGAA | 51455 |
| rs756244892 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99423945 | AGCACATGAACAATT[C/T]TGGCAATACAAAACT | 51455 |
| rs756263924 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425368 | GCTAAGTCCCTAGTA[A/G]ATAAGAAATACCTAA | 51455 |
| rs756272282 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99455744 | AGAGAATCCTCTCCT[-/A]AAAACACCACATTTG | 51455 |
| rs756291487 | snp | C/T | 1.89138e-05 | 0.00307515 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403063 | CTTGTTTCTTTTCTT[C/T]TCTTTCACTGCTGCC | 51455 |
| rs756303107 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410534 | CCAAGTGCATTAACC[A/T]AAGCTGAATGCCTTG | 51455 |
| rs756353670 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99411309 | GTAAAACTACAACAA[A/C]AAAAACTGTTTGGTA | 51455 |
| rs756363620 | snp | A/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404648 | TTCCCGGAGATCAGG[A/T]GGAAGTGCTTCTAAA | 51455 |
| rs756380447 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447318 | GCTGGGACTACAGGC[A/G]CGCGCCACCACGCCC | 51455 |
| rs756399485 | snp | C/T | 3.30846e-05 | 0.00406709 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406343 | CTTTGTGCTCCTCTT[C/T]GGTGGATTTCTTAGC | 51455 |
| rs756401282 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412788 | TTTTCTTTCCTTTTC[A/G]GTTCGAACTGGTCTA | 51455 |
| rs756440705 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476044 | ATCTAGTTTTAAAAA[C/T]GCTTTCAACAAACAC | 51455 |
| rs756509539 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444421 | GACAGCATGCTGGAG[A/T]GATGCAGACTCTACA | 51455 |
| rs756520584 | snp | A/G | 1.75391e-05 | 0.00296129 | intron-variant | REV1 | GRCh38.p7 | 2:99405894 | TGTACTTATATTTAG[A/G]ACTACAAAAATGTAC | 51455 |
| rs756536479 | in-del | -/GAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99407453 | GCTACTCGGGAGGCT[-/GAA]GAAGGAGAATTGCTT | 51455 |
| rs756539041 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448129 | CTCCGTGAATTTATG[C/T]GGCTAAATACACTAT | 51455 |
| rs756597192 | snp | A/G | 1.65343e-05 | 0.00287521 | intron-variant | REV1 | GRCh38.p7 | 2:99412722 | CAAAATCTGTTCAAT[A/G]ATCAGTACCTGAGTA | 51455 |
| rs756603408 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434390 | CAGCTGGGGGTTAGC[A/G]CCAGGACGTAAAGGT | 51455 |
| rs756614476 | snp | A/G | 1.64844e-05 | 0.00287087 | intron-variant | REV1 | GRCh38.p7 | 2:99464885 | GAAAAATAACTAGAC[A/G]GTTCGATATAATTAT | 51455 |
| rs756663906 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99445041 | TTACATTCTATACAA[C/T]GAATCAAAACATAGT | 51455 |
| rs756671512 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433299 | CTACTCATGACACAC[A/G]AAATTCTAGAATCTC | 51455 |
| rs756686318 | snp | A/G | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424257 | GCATGCCCAAAAAAC[A/G]TTCCGTTCTTAATGC | 51455 |
| rs756749796 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430647 | AACTGGAGCCTAGTG[C/T]GGCTTACCAACATCT | 51455 |
| rs756817457 | in-del | -/T | 1.65173e-05 | 0.00287374 | intron-variant | REV1 | GRCh38.p7 | 2:99462662 | ATCACAAAGGTTACA[-/T]TTTTCTCCCCCCTTT | 51455 |
| rs756854550 | in-del | -/CA | | | intron-variant | REV1 | GRCh38.p7 | 2:99409345 | TCATATACATGAATG[-/CA]CACCATGTATGGTTG | 51455 |
| rs756873478 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469221 | ATGCTTTTTTTCCCC[C/T]GTAAGTTTTAGGTTT | 51455 |
| rs756885121 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99416261 | ATTACTAGTCTTTAA[A/C]AAAGATAAATAGGTT | 51455 |
| rs756912132 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99431606 | GTATCTGAAGGGCTA[A/G]TTATCTAAGATATTG | 51455 |
| rs756914997 | snp | C/G | 1.66913e-05 | 0.00288883 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402624 | TCAGCCTTGGGCCAT[C/G]TAACACAGGCCAAGC | 51455 |
| rs756942934 | snp | A/C | 1.65721e-05 | 0.0028785 | intron-variant | REV1 | GRCh38.p7 | 2:99421696 | TCACAGCCACAGCCA[A/C]CATCTGGTAGACCCA | 51455 |
| rs756951991 | snp | C/T | 4.96446e-05 | 0.00498195 | intron-variant | REV1 | GRCh38.p7 | 2:99442494 | AAAGCAACACCAATT[C/T]AGAGTTCCATACTTG | 51455 |
| rs756974786 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99417265 | GTGCCTCAGCCTCCT[C/G]AGTAGCTGGGACTAC | 51455 |
| rs756986228 | snp | C/T | 4.94898e-05 | 0.00497418 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438849 | GAAGTGCTTTTTGTG[C/T]TTGAAGGCCCCTGAA | 51455 |
| rs757010983 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99469982 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGTCACCT | 51455 |
| rs757039729 | snp | C/T | 3.29745e-05 | 0.00406031 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435911 | ATTATACAGCTCTGA[C/T]GTCTGGGAGAATTCA | 51455 |
| rs757043777 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454921 | CGTTTAGACCTAAAG[C/T]CCTACAAGTAAAATG | 51455 |
| rs757106472 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468990 | ATACGGACTCAAATC[C/T]CAATTCTACGACTGC | 51455 |
| rs757155277 | snp | A/G | 1.71502e-05 | 0.00292827 | intron-variant | REV1 | GRCh38.p7 | 2:99412994 | CAGAATAAGCTACTA[A/G]TAACAAGTTTATTAA | 51455 |
| rs757155675 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481421 | TAGTAATTCTCAACA[C/G]AAGGCAATCCTTCTA | 51455 |
| rs757176462 | in-del | -/AG | 1.67486e-05 | 0.00289379 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401214 | TATGGCACAGCTATC[-/AG]AGAGCATCAGGCTCT | 51455 |
| rs757179365 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403711 | AGATGCGCTGGCTGA[C/G]TGCTGGTGAGTGCTG | 51455 |
| rs757211236 | snp | C/T | 1.69175e-05 | 0.00290834 | intron-variant | REV1 | GRCh38.p7 | 2:99408168 | AACAAAAGCTTCATT[C/T]CATATGTATTCACTA | 51455 |
| rs757230545 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416498 | AAAACCACATGAACC[A/G]CTGTGAGCAATACAG | 51455 |
| rs757235278 | in-del | -/TTTTT | | | intron-variant | REV1 | GRCh38.p7 | 2:99473641 | TTGCCACTTTATGTG[-/TTTTT]TTTACACCTTCAGCA | 51455 |
| rs757245167 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99424097 | TTGAACTGTCTTTAC[G/T]ATTAGCTAAAAGAAG | 51455 |
| rs757249295 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440223 | GAAATGCATTCACGA[A/G]AATCATCTAAGTAAC | 51455 |
| rs757274466 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482395 | TGCGAGTCATTCTAC[C/T]AAATTATCAAACGTG | 51455 |
| rs757279027 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461527 | GAGACCTGAAAGATA[C/G]CAGGTATCAGCCAGC | 51455 |
| rs757304343 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438990 | TGCAACTGCTGCAGA[A/G]TGCAGTCTCTGAAAT | 51455 |
| rs757342869 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99425589 | CAGTTTAGACATATA[C/T]GTAGAAACATAAAAT | 51455 |
| rs757378584 | snp | A/G | 1.65179e-05 | 0.00287379 | intron-variant | REV1 | GRCh38.p7 | 2:99402830 | AAGGATAAAATTGCT[A/G]TATTCACACATTATC | 51455 |
| rs757384733 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99411746 | TCACTGACTTGTCGA[A/C]AATTCTTTTGTAACT | 51455 |
| rs757465244 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448497 | AACAGCAGAGAAACC[A/T]CAATATAATCATTAA | 51455 |
| rs757504902 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433632 | TCTAACTTCTGACTA[C/T]TTTCTGGGTAATATA | 51455 |
| rs757535517 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418869 | CTGATAAAATCATCT[A/G]CTTCTTCTGGTTTTA | 51455 |
| rs757551748 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99410998 | AGCATCTATTAAAAA[C/G]AAACGTGGCCAGGCG | 51455 |
| rs757559498 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99449081 | GAGTTTGAGACCAGT[A/C]TCGGCAACATGGTGA | 51455 |
| rs757606989 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409188 | TATCATAACAGGTAG[A/G]TAAATATAATTCAAG | 51455 |
| rs757639483 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452727 | CTAAATTCATTAACA[A/T]CCTCAATGCATCCCA | 51455 |
| rs757669614 | snp | A/C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434870 | GCAACAGAAACTAAA[A/C/T]ACATATGCATAGGAA | 51455 |
| rs757670937 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402960 | GGGGACTGCCACAGG[C/T]CCCTGGCAGAGTTTT | 51455 |
| rs757693853 | snp | C/T | 1.67942e-05 | 0.00289772 | intron-variant | REV1 | GRCh38.p7 | 2:99412690 | GACTATGTAAAAATA[C/T]AAAGAGCAACAGATG | 51455 |
| rs757694477 | in-del | -/G | 1.65031e-05 | 0.00287251 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438874 | CCTGAACAGTGGAGT[-/G]GTGAGCACCATTGAT | 51455 |
| rs757711000 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467649 | CCAAGGATAAAGATT[C/G]CCGCAATTGCTATCA | 51455 |
| rs757715955 | snp | A/C | 1.66899e-05 | 0.00288871 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429927 | TCTGGATTCTCCCAC[A/C]ATGATGAATCTGGTA | 51455 |
| rs757744497 | snp | C/T | | | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479872 | CAGCCATAAATCTCA[C/T]GTTCGAGAAGACACC | 51455 |
| rs757750092 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404545 | CAACTGGTTGTGGCA[A/C]AATTCCTGTATTACA | 51455 |
| rs757765628 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425965 | CGCTTGAACCTGGAG[A/G]GTGGAGGTTGCAGTG | 51455 |
| rs757797576 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438786 | AAATTGCAGTCTGAA[A/G]GTTTGGATGGCACTG | 51455 |
| rs757798941 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99465847 | CGTCAAATCAGCTCT[A/G]ATATGATCTATGAGA | 51455 |
| rs757871117 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417460 | CAGTGTGACTGTATT[C/T]GGACACAGAATCTTT | 51455 |
| rs757909743 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407755 | ATATCTACTTCTAGG[A/G]AACAAGAACAGGGAA | 51455 |
| rs757917888 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431779 | CGTGGGTCCCTCCAC[A/G]AGCGGAGTGAGTTGC | 51455 |
| rs757925939 | snp | A/G | 3.30202e-05 | 0.00406313 | intron-variant | REV1 | GRCh38.p7 | 2:99401362 | ATCAGCCTAAAGGTG[A/G]GGAGAGAAGAAATGT | 51455 |
| rs757941649 | snp | A/C/T | 0.000167512 | 0.00915048 | intron-variant | REV1 | GRCh38.p7 | 2:99421681 | AGCAAAGGCAACGAA[A/C/T]CACAGCCACAGCCAC | 51455 |
| rs757987656 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462517 | ATCCATTAACATAGA[C/T]GGCAACTCCACTAAA | 51455 |
| rs758011802 | snp | A/C | 5.52379e-05 | 0.00525508 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402269 | ATTTTATAACTAGAT[A/C]CAGTTTTTCCAAATC | 51455 |
| rs758012060 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422672 | CTGAGATAGGATTTC[C/T]CAAGGGTGGTAGAAG | 51455 |
| rs758045557 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419143 | ACAGAGGTTTCTCTT[C/T]GCTCTAACGCAAGTG | 51455 |
| rs758057339 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491741 | TAAATGGCAGCATTC[C/T]TGCACGATTGTATTT | 51455 |
| rs758065257 | in-del | -/AAAG | | | intron-variant | REV1 | GRCh38.p7 | 2:99423994 | ACCTGGAAATTGCCC[-/AAAG]AAAGGTCTCAAACTG | 51455 |
| rs758067838 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455088 | CAAAAGCTTTCCTAG[C/T]TAGATCTCTATTGAG | 51455 |
| rs758069148 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468947 | TCAGTTATCCATGGT[C/T]TACAACATAATGATA | 51455 |
| rs758074086 | snp | A/T | 1.65908e-05 | 0.00288012 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438636 | GCAGACCTGCCTGTT[A/T]TCATTTTTTTTAACT | 51455 |
| rs758155798 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440525 | GCTAAACATCATATG[G/T]AATGTGACAGGCAAC | 51455 |
| rs758244665 | snp | A/C | 2.61011e-05 | 0.00361246 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439359 | TCTGACTTTTAGGTT[A/C]AAACAATTTTTTCAT | 51455 |
| rs758248883 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480231 | GGGAGAGTGGGATGG[A/G]AGAACTGCTTGAGCC | 51455 |
| rs758253461 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414438 | CAAGTAAATACCAAA[A/G]ACCCCGAGTTAACAA | 51455 |
| rs758283302 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461329 | TCCAGTCACTGTAGA[A/G]GCACTAAGGATATAG | 51455 |
| rs758299966 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425725 | GTTTACAAATTAAAG[A/G]TAACACATTTTTTAA | 51455 |
| rs758315802 | snp | G/T | 1.64928e-05 | 0.00287161 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424237 | GATTAGGACATAGTT[G/T]TTTAGCATGCCCAAA | 51455 |
| rs758324395 | in-del | -/T | 8.90908e-05 | 0.00667364 | intron-variant | REV1 | GRCh38.p7 | 2:99402209 | CATTGTGACATGCCA[-/T]TTTTTCCCATTTGAT | 51455 |
| rs758334789 | snp | C/T | 1.65012e-05 | 0.00287234 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434418 | GGTGCCCTTCCTGTG[C/T]CTCTGTTACTTGTAA | 51455 |
| rs758370983 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99442604 | AGTTTATTCCTTCTT[A/G]CTCGGTTTTAGTGGT | 51455 |
| rs758395234 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472983 | ACAGTTTTCAAACAA[C/T]TGCTGAAGTTGTACG | 51455 |
| rs758401698 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99474827 | CAATCACTTGAACGC[G/T]GTAGGCAGAGGTTGC | 51455 |
| rs758424563 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448585 | TAGGTCCACATTATC[C/T]TGATGTATTACCATG | 51455 |
| rs758440640 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99434758 | GGAAAGAGGCAACTC[-/TT]AAGAGTCTAGATTCA | 51455 |
| rs758453296 | snp | C/T | 3.29565e-05 | 0.00405921 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99464956 | TTTTCAGCTCGCTTC[C/T]TCCATCCACCTCGCC | 51455 |
| rs758454346 | snp | A/C | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418851 | TTGGTCACTAGCTGG[A/C]CTCTGATAAAATCAT | 51455 |
| rs758462969 | snp | A/G | 1.66932e-05 | 0.002889 | intron-variant | REV1 | GRCh38.p7 | 2:99412961 | CAACTCCTAGGAAAG[A/G]GAATATAGTTAAGTA | 51455 |
| rs758478503 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99413187 | ATAGATGAACCAGAA[A/G]CTTTTAAAATATGTA | 51455 |
| rs758487068 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486841 | AAAGCTGTGTACAAG[A/T]CAGACAAGACCTCTG | 51455 |
| rs758495678 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488475 | TCAAAAGGTCCTACA[C/T]AGTAAGAGAAGACAG | 51455 |
| rs758514650 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99449251 | GCCTGGGCGACAAAG[C/T]GAGACCCTATCTCAA | 51455 |
| rs758555264 | snp | G/T | 6.59152e-05 | 0.00574049 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405991 | ACCATTCCATTTCCC[G/T]GAAGACTCAGCCTTG | 51455 |
| rs758562897 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412817 | TATCATCCAAGCCAC[A/G]GCAGAACCTATAAAG | 51455 |
| rs758563538 | in-del | -/AAAGG | | | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402460 | TCACTAACAGCTATC[-/AAAGG]AATGGGCTTTGTTAC | 51455 |
| rs758670044 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99484925 | TCTGTTTCTTTATAA[C/T]GGTGCCAACCTTATA | 51455 |
| rs758715230 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99407905 | CTTTTCCTTGTATTA[C/T]AAAGCAGCTAAAGAC | 51455 |
| rs758732903 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99461612 | CACTTCAAAAAATAC[A/C]ATGAAATGATAAGAA | 51455 |
| rs758754105 | in-del | -/TCT | 1.65081e-05 | 0.00287293 | cds-indel, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439236 | AAATCATTATTTTCA[-/TCT]TCTTCATTCCAACTG | 51455 |
| rs758763910 | in-del | -/CT | | | intron-variant | REV1 | GRCh38.p7 | 2:99462674 | TACATTTTCTCCCCC[-/CT]TTTTTGAAAAAAAAA | 51455 |
| rs758831927 | snp | A/C | 1.64988e-05 | 0.00287213 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438979 | TGGTGCTTTGCTGCA[A/C]CTGCTGCAGAGTGCA | 51455 |
| rs758837489 | snp | A/G | 0.000116245 | 0.00762293 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429906 | ATTCCATTTGCTTGC[A/G]CAGAATCTGGATTCT | 51455 |
| rs758874041 | snp | A/C | 1.77021e-05 | 0.00297502 | intron-variant | REV1 | GRCh38.p7 | 2:99410664 | CTGTACTGAAATATA[A/C]TTACCAATATCATTT | 51455 |
| rs758878525 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99451949 | GGAAGCTACCCTATT[C/T]TGAATTTTTTTTTTT | 51455 |
| rs758889211 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486407 | GGTGGCAGGTGCCTG[C/G]AGTCCCAGCTACTCG | 51455 |
| rs758902128 | snp | C/T | 3.2963e-05 | 0.00405961 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402688 | AAGGTCTTCACATCA[C/T]TGAATTCAACAGCTC | 51455 |
| rs758950451 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99442841 | ACTGTAAAATAAAAA[-/T]ATAGGACAAAATAAA | 51455 |
| rs758954535 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99442698 | TTTAAACCTCATGAC[-/TT]TAGTATTTACCACCC | 51455 |
| rs758967649 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476090 | CTTTACGTAACTTTT[C/T]CTATGCTTGCCAAAA | 51455 |
| rs758992098 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99453310 | TTGCAATGAGCTGAG[-/A]ATTGTGCCACTGCAC | 51455 |
| rs759106862 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436439 | AGTTTAAGTCACATA[A/G]CCTATTATTAAATGG | 51455 |
| rs759134665 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99420585 | GGTGCTTCCCCAGTA[G/T]TCCTGTGTAGCACGG | 51455 |
| rs759142592 | snp | A/G | 3.29761e-05 | 0.00406041 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412756 | CTTATTCCATAGTTG[A/G]TCTCAGCTGAAACAG | 51455 |
| rs759149913 | snp | A/G | 1.64857e-05 | 0.00287099 | intron-variant | REV1 | GRCh38.p7 | 2:99462487 | AGGGTTAAGTAAAAA[A/G]TACTCAACCTGTGTA | 51455 |
| rs759151243 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461997 | AATAGAGAGACTAAG[G/T]GAAATTTTACTTCCT | 51455 |
| rs759163700 | snp | G/T | 1.66668e-05 | 0.00288672 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403037 | TTTGGTGAACCAATG[G/T]TTTTTTTCTTCTTGT | 51455 |
| rs759164769 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99408706 | TCAAAGATGTGCTGA[A/C]CTCACCCACCATTTC | 51455 |
| rs759209603 | snp | A/C | 1.72653e-05 | 0.00293809 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439300 | TTTCAATCTTCTTAA[A/C]GATGTGATTTCTAAA | 51455 |
| rs759222702 | in-del | -/TTTCT | | | intron-variant | REV1 | GRCh38.p7 | 2:99450784 | ATCTGAGATATTTAC[-/TTTCT]TTTTTCTTCTTAAAT | 51455 |
| rs759229633 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421699 | CAGCCACAGCCACCA[C/T]CTGGTAGACCCAATG | 51455 |
| rs759235414 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99475513 | CAGATGGGGAGGAAA[A/G]TCTTTGAAGAGGTAC | 51455 |
| rs759267102 | in-del | -/TATAACAA | 1.85304e-05 | 0.00304382 | intron-variant | REV1 | GRCh38.p7 | 2:99435788 | CTTTGAATATATATT[-/TATAACAA]TATATCAGTTTTCTT | 51455 |
| rs759285317 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99461115 | TACACAGAAAAGTTA[A/C]AAGCTTTCTGCATGT | 51455 |
| rs759353893 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444660 | TGCACTACAGTAATG[C/T]TAGTGAAGTAATGTC | 51455 |
| rs759354469 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99427331 | GATCTGTGATTCTAG[C/G]ATATCTGTGTATCGT | 51455 |
| rs759373048 | in-del | -/AC | 5.37177e-05 | 0.00518227 | intron-variant | REV1 | GRCh38.p7 | 2:99442275 | AAAAAAAAAAAAAAA[-/AC]ACCAACCAGCTTTGC | 51455 |
| rs759381366 | snp | A/G | 5.83686e-05 | 0.00540193 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402390 | GACCAGTCTTTTTGA[A/G]GGAGAAAGTCAGAGA | 51455 |
| rs759402086 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | REV1 | GRCh38.p7 | 2:99462639 | TAGAATTAAAGAAAA[A/G]GTAAACCAATCACAA | 51455 |
| rs759451154 | snp | A/G | 1.7187e-05 | 0.00293142 | intron-variant | REV1 | GRCh38.p7 | 2:99402226 | TTTTCCCATTTGATA[A/G]AAGTGATGAATTACT | 51455 |
| rs759457581 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99431310 | TTTCTGACATATGAA[A/T]AACGTATGCTAGCTA | 51455 |
| rs759491510 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430242 | TCCTATAACACACAG[A/T]CCCTGGAGGTGGACA | 51455 |
| rs759543395 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416805 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51455 |
| rs759559302 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440768 | ACCCCAGAAAACAAC[-/AAA]AGTGATGTACGTCAG | 51455 |
| rs759560295 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99418285 | TCCTGCCCCTTAGGT[A/G]AGAAAGGTTAAGATG | 51455 |
| rs759569824 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403771 | CGCTGCTTTCAGCTC[C/T]CTCTGAAGTTCAGCA | 51455 |
| rs759570096 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453033 | ATTAAGAGCTAAAAA[G/T]TATAAATTACTGAGA | 51455 |
| rs759581602 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415944 | TTTCATTAGGTAACC[A/G]GATCATATTAAGAAA | 51455 |
| rs759584414 | snp | A/G | 1.85779e-05 | 0.00304772 | intron-variant | REV1 | GRCh38.p7 | 2:99435783 | AATCTCTTTGAATAT[A/G]TATTTATAACAATAT | 51455 |
| rs759607715 | snp | A/G | 1.65427e-05 | 0.00287595 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405939 | GGACCTCTATACTCA[A/G]GTTAAGTCTCGACTG | 51455 |
| rs759650770 | snp | C/T | 3.29772e-05 | 0.00406048 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442332 | ACCCTGTTGTTGAGC[C/T]GTTTGGCTATATTGC | 51455 |
| rs759661878 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99438473 | ATGCTTACTGTAACT[G/T]ACATGATTTGACATA | 51455 |
| rs759667606 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99421740 | GTCTTCTTATCCTCT[-/C]TTTTTTCTATTTCCT | 51455 |
| rs759711041 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461598 | TATTTACAGCCATTC[A/G]CTTCAAAAAATACAA | 51455 |
| rs759721311 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478167 | CTTAAACCCGGGAGG[C/G]AGAGGTTGTAGTGAA | 51455 |
| rs759727235 | snp | C/T | 3.29554e-05 | 0.00405914 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442443 | AGCTGATATGGAATG[C/T]AGGAGAGGAGTCGTC | 51455 |
| rs759747955 | snp | A/G | 5.05455e-05 | 0.00502695 | intron-variant | REV1 | GRCh38.p7 | 2:99424318 | TGGAGGTTATTCTAG[A/G]AAGTTTTCAACTCAA | 51455 |
| rs759754631 | in-del | -/CT | 8.24137e-05 | 0.00641873 | intron-variant | REV1 | GRCh38.p7 | 2:99403652 | ACAGTGACTCCATTA[-/CT]CTTTGTCTTCATTTT | 51455 |
| rs759772090 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99488717 | TGGTTCCCACAGGCT[A/G]ATTTGCTACATACAG | 51455 |
| rs759787685 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454663 | GGCAGGAAGATCCGT[A/T]GAGCTCAGGAGTTTG | 51455 |
| rs759788711 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403886 | GTTTCTCTTTTTCAC[A/G]AAACAGACTTTGTTT | 51455 |
| rs759796614 | in-del | -/AAT | | | intron-variant, upstream-variant-2KB, cds-indel | REV1 | GRCh38.p7 | 2:99479783 | CAAAAAAGTAAAAAT[-/AAT]AATAATAATAATAAT | 51455 |
| rs759801887 | snp | A/C | 5.17558e-05 | 0.00508677 | intron-variant | REV1 | GRCh38.p7 | 2:99406535 | AGGAAAACTAAAGTG[A/C]AAATATGAATTCAGC | 51455 |
| rs759839453 | snp | C/T | 1.66704e-05 | 0.00288703 | intron-variant | REV1 | GRCh38.p7 | 2:99418976 | AAGTCATCCAAGAAA[C/T]AGTCACAATTATTTT | 51455 |
| rs759839637 | snp | A/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440886 | GGCAGGAAAATACAT[A/T]GTTAACATACATTCT | 51455 |
| rs759855432 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99416919 | TCCATCTCAAAAAAA[-/AA]AAAAAAAAAAAAAAG | 51455 |
| rs759882165 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405029 | TCCCACCCCAGGGAG[A/G]GGTGAAGGCCTGAGG | 51455 |
| rs759915775 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425165 | TTACTACACAGCATG[C/G]AGACGTGCCTTGTTT | 51455 |
| rs759973400 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461399 | CAACTATGGAAAGGT[C/T]TGAAGAATTCTAAGA | 51455 |
| rs760069722 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | REV1 | GRCh38.p7 | 2:99404432 | AGCAGAGGGTTCCCA[C/T]ATTTAACTTACCTGT | 51455 |
| rs760113371 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99460922 | GCAATATTCATTTTT[A/C]TTCCCTCACACAAAG | 51455 |
| rs760137291 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436633 | TTTAAGGAGATAAAG[G/T]TGAGTGTCCTCACCT | 51455 |
| rs760172163 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99470957 | AAGCATTCCAAAGAG[C/G]TTTATCCTATCTTTA | 51455 |
| rs760190197 | snp | A/G | 3.30306e-05 | 0.00406377 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439128 | CCATTAGAGCTAGGA[A/G]TGTGTCCATTAAAAA | 51455 |
| rs760249704 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99423294 | GGCAGAGGTGAAAAC[A/C]GAGGCAAGAAGTCTA | 51455 |
| rs760279696 | in-del | -/ATTT | 0.000115032 | 0.00758305 | intron-variant | REV1 | GRCh38.p7 | 2:99449303 | ATTCTAACTTTAAAA[-/ATTT]ATTAATTAAATTTAA | 51455 |
| rs760291718 | snp | C/T | 1.71505e-05 | 0.0029283 | intron-variant | REV1 | GRCh38.p7 | 2:99406274 | ACCAACTGCCGTCTT[C/T]CCAAGGACATAAGCA | 51455 |
| rs760309392 | snp | C/T | 2.4542e-05 | 0.00350291 | intron-variant | REV1 | GRCh38.p7 | 2:99429972 | ATAAAAAAAAATTAA[C/T]GGTTATATGTTATAA | 51455 |
| rs760366670 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99410039 | TTTTTGAGACAGAAT[A/G]TTGCTCTGTTGCCCA | 51455 |
| rs760379547 | snp | A/G | 3.30202e-05 | 0.00406313 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402918 | CAGGAGGTCCTTCAT[A/G]TTTTAGAAACCCATC | 51455 |
| rs760426620 | snp | C/G/T | 3.30312e-05 | 0.00406383 | intron-variant | REV1 | GRCh38.p7 | 2:99462463 | CCTAATAAAAATACA[C/G/T]GCCAAAATAGGGTTA | 51455 |
| rs760457600 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486202 | ATCCTAAGTGAACAA[A/G]CTAATTTCAAATAGT | 51455 |
| rs760487984 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99431341 | TACTATTACAAATTA[A/C]AGACAGAATCCCAAG | 51455 |
| rs760496438 | snp | C/T | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401286 | TTGTTGTAAAACCAC[C/T]TGGACATTGTCAAGA | 51455 |
| rs760554787 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477977 | GTGGCTCACACCTGT[A/T]ATCCCAAGACTTTGG | 51455 |
| rs760568236 | snp | A/G | 4.94271e-05 | 0.00497102 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438741 | ATTGATATGTGATGC[A/G]GTCTTGAATGAGAAT | 51455 |
| rs760575924 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432473 | GAGGAACAAAAGCAC[C/T]GAAAAAAGTTCTGAG | 51455 |
| rs760577974 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417066 | TTAAAGATGGTGTTT[C/T]GGACTAAACTGTGTC | 51455 |
| rs760603275 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491243 | AGATTGCATACTTTT[C/G]AAAGACGTCATAATT | 51455 |
| rs760614282 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424169 | TGCCAATGTTTCATA[C/T]AATGTTTGTGCGACT | 51455 |
| rs760619123 | snp | C/T | 1.65315e-05 | 0.00287498 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449482 | CAACATCATTAGTTT[C/T]CTCAATTCCTCAGCG | 51455 |
| rs760631793 | snp | C/G | | | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424210 | CATGAAAATCGTATG[C/G]AACAGCTTGAAGATT | 51455 |
| rs760667914 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99418387 | GCTCACACACATTCT[A/C]TTTATACTTTTAAAA | 51455 |
| rs760677780 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99405366 | TTTCCCCTAGTTTTG[C/T]AGCCAGTATTTAACA | 51455 |
| rs760703922 | in-del | -/CA | | | intron-variant | REV1 | GRCh38.p7 | 2:99459207 | AGTGAGACTCTGTCT[-/CA]AAAAAAAAAAAAGAA | 51455 |
| rs760704298 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99431209 | CGGCAACCATATATA[A/C]ACAGCATAAATGCAA | 51455 |
| rs760713288 | snp | A/C | 1.98454e-05 | 0.00314997 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439325 | TCTAAAGCAGGAAAA[A/C]ATTTTTGAGTTAATA | 51455 |
| rs760726976 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99404210 | TCAGTGTGTTTCTGT[C/T]TTAGCATGCCCTCCC | 51455 |
| rs760746896 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464860 | TTAAACCACATTATA[A/G]CAGAAGAATGAAAAA | 51455 |
| rs760746925 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99479206 | GGTGGCACTCCCCTG[C/T]AGTCCCAGCTACTTG | 51455 |
| rs760772226 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468747 | AATTAGTTTAAAAAA[C/T]GGATGAAGAGTGAAT | 51455 |
| rs760777497 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454854 | CATAGTGACAGACAA[C/T]TGAAAGCACAGTAAA | 51455 |
| rs760779228 | snp | C/G | 8.24872e-05 | 0.00642159 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406409 | ACCCACTAGGAAAGT[C/G]GCTTGACTGAACTGA | 51455 |
| rs760802389 | in-del | -/TT | 1.6902e-05 | 0.00290701 | intron-variant | REV1 | GRCh38.p7 | 2:99421469 | ATCTCAAAGCAACTC[-/TT]TTGAGTACAAGATAA | 51455 |
| rs760834746 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478109 | TGGTGGTGCACACCT[A/G]TAGGTAGTCCCAGCT | 51455 |
| rs760867506 | snp | A/G | 1.65567e-05 | 0.00287716 | intron-variant | REV1 | GRCh38.p7 | 2:99406514 | CAGAATAAAGAGTAT[A/G]CTTCTAGGAAAACTA | 51455 |
| rs760869164 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440035 | TAGAAAAATAAGGAC[A/G]CTTGCCTTACTGAGA | 51455 |
| rs760933079 | snp | A/G | 1.77335e-05 | 0.00297765 | intron-variant | REV1 | GRCh38.p7 | 2:99402205 | CAGCCATTGTGACAT[A/G]CCATTTTTTCCCATT | 51455 |
| rs760948084 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458820 | TTGAAATGACAAAAT[A/T]ATAAAAATGGAGACC | 51455 |
| rs760949368 | snp | A/G | 1.65053e-05 | 0.0028727 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421652 | CAATGTTATGAGTGT[A/G]GCTATCAACACAGAG | 51455 |
| rs760955385 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99441124 | GAAAGCTAAAGCTAC[A/G]TATTCTGTGAAAAGG | 51455 |
| rs760956485 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470786 | TAGCAGCAGGGTGGA[C/T]GCATCAGGTTATAAA | 51455 |
| rs760964179 | snp | A/G | 1.69821e-05 | 0.00291389 | intron-variant | REV1 | GRCh38.p7 | 2:99434487 | TTCTGTATGTGGTAC[A/G]GGAATGTTAACAACA | 51455 |
| rs761035935 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99457408 | TTATATAGGTCAGGT[C/G]CACTGGCTCACACCT | 51455 |
| rs761038922 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483959 | TTGAGAAGCCAATAA[C/T]TCATAATTTAGATAT | 51455 |
| rs761051153 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413911 | GGTGTGGTGGCTCAC[A/T]CCTGTAATCCCAATA | 51455 |
| rs761052349 | snp | C/T | 4.94621e-05 | 0.00497279 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435862 | TCTATTTCGTATACC[C/T]ACTGATACAAAGAAG | 51455 |
| rs761112202 | in-del | -/AAATT | | | intron-variant | REV1 | GRCh38.p7 | 2:99417923 | TTATAAAGTATTCTC[-/AAATT]AAATGTGAAACTAAC | 51455 |
| rs761139238 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487281 | CGACTAAGATTCAAA[C/T]GTAAGTGGTTCACAG | 51455 |
| rs761239874 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | REV1 | GRCh38.p7 | 2:99403669 | CTTTGTCTTCATTTT[C/T]GTTACATGCCACTTC | 51455 |
| rs761285866 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482392 | GTCTGCGAGTCATTC[C/T]ACCAAATTATCAAAC | 51455 |
| rs761325438 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403757 | TGTCTTTGATCATAC[A/G]CTGCTTTCAGCTCCC | 51455 |
| rs761339709 | snp | A/G | 1.64936e-05 | 0.00287168 | stop-gained, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405954 | GGTTAAGTCTCGACT[A/G]CACACTGACAGGAGT | 51455 |
| rs761342838 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430743 | ACTGGCTGCATGCCA[C/G]TTTACTTCCTTTGCC | 51455 |
| rs761370730 | snp | C/T | 1.65097e-05 | 0.00287308 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438945 | GTTCTGTGTGGATTC[C/T]GCAAAGCATCTGTGT | 51455 |
| rs761389867 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402777 | AAGGCCTGGCACACC[C/T]GAAGTAGAAGCAGAG | 51455 |
| rs761392034 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411002 | TCTATTAAAAAGAAA[C/T]GTGGCCAGGCGCGGT | 51455 |
| rs761425588 | snp | C/T | 1.66255e-05 | 0.00288314 | intron-variant | REV1 | GRCh38.p7 | 2:99418807 | CTGTAATAAAAGTAT[C/T]GTTAAAATATTTCTA | 51455 |
| rs761437272 | snp | C/T | 0.000121234 | 0.00778475 | intron-variant, missense | REV1 | GRCh38.p7 | 2:99424825 | GTGGCTCCACAGTGG[C/T]TGAGATGCCAACAGC | 51455 |
| rs761498518 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405275 | GCAATCCCATCAACT[A/G]GGTGGACCAATCTTA | 51455 |
| rs761584244 | snp | A/C | 1.65064e-05 | 0.00287279 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406042 | CAGATGTGCAGGAAA[A/C]GGTGGCAAGAAAGTG | 51455 |
| rs761612908 | snp | A/T | 2.22511e-05 | 0.00333543 | intron-variant | REV1 | GRCh38.p7 | 2:99429966 | TTAAAAATAAAAAAA[A/T]ATTAATGGTTATATG | 51455 |
| rs761635955 | snp | A/G | 1.65291e-05 | 0.00287476 | intron-variant | REV1 | GRCh38.p7 | 2:99402866 | ATATTAAGATCTCAT[A/G]AAGGTCAAAGTTAAG | 51455 |
| rs761678468 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464635 | TTATTGGATATTTAT[A/G]TGTTTTCCTGTTTTT | 51455 |
| rs761684531 | snp | A/T | 0.000119304 | 0.00772256 | intron-variant | REV1 | GRCh38.p7 | 2:99434306 | TCCACAGGAGCACTA[A/T]GACTTCAAAGAGAGC | 51455 |
| rs761700172 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405759 | TATTTAGAATCCAAC[A/G]TCATGATCTACCCAA | 51455 |
| rs761707472 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447803 | CAGCTCACTGGAGCC[A/T]CCCATCTCCTGGGTT | 51455 |
| rs761736197 | snp | C/G | 1.64814e-05 | 0.00287061 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438706 | GGGTATTGACAAACT[C/G]AGTCAATTCACACTT | 51455 |
| rs761772291 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99420274 | AAAATCCTGCTGGCT[A/G]GGGAGAGACTGCCCT | 51455 |
| rs761797939 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99478042 | GTTCGAGACCAGCCT[G/T]GCCAAAATGGCAAAA | 51455 |
| rs761798657 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456101 | TAAACATGCCCAGAG[C/G]CTACCTCCCAGATTA | 51455 |
| rs761858511 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426689 | GACAATTACAAAAAA[G/T]TCCAAAGTGTCTCAA | 51455 |
| rs761890034 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476786 | CAAGGCTTGGGTGAG[C/T]TTCCCTGATAGGCAA | 51455 |
| rs761892310 | snp | A/G | 1.65943e-05 | 0.00288043 | intron-variant | REV1 | GRCh38.p7 | 2:99401389 | ATGTCATTAGGAATT[A/G]GGAAAGGTCCTTAAG | 51455 |
| rs761918245 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99441508 | TAGTCTAGATTCACT[C/T]TCAATTCTATAACCA | 51455 |
| rs761920653 | snp | A/C | 1.65814e-05 | 0.00287931 | stop-gained, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421505 | GATACTAACCAATTC[A/C]AACAGAGGCAGCACA | 51455 |
| rs761928190 | snp | C/T | 1.65452e-05 | 0.00287616 | intron-variant | REV1 | GRCh38.p7 | 2:99462448 | CAAATCATTCTCAAT[C/T]CTAATAAAAATACAT | 51455 |
| rs761975853 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491984 | AGAGAGATGGGGAAT[A/G]CATAAATAAAAATGT | 51455 |
| rs761988376 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99457225 | GCAGCATCCAAAATA[C/T]ATCTGTTCAATCAAC | 51455 |
| rs761996646 | snp | A/C | 1.68168e-05 | 0.00289967 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401190 | CTTTGCAAATACCTC[A/C]CAAGCACTTATGGCA | 51455 |
| rs762008198 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99442990 | ACAGCATATCACACA[A/C]CACCACTCAAATCCA | 51455 |
| rs762010195 | snp | C/T | 3.29571e-05 | 0.00405924 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421610 | TTTCGGTAATGTCTA[C/T]CAGCGCTTCATCACA | 51455 |
| rs762010335 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99426775 | AATTACCAAAACTTC[A/G]TTAAGTGTATGCTGC | 51455 |
| rs762078221 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469628 | TTTCCATTCTCTCAA[C/T]AGGGATGTTCAAAAC | 51455 |
| rs762086858 | snp | C/T | 8.24423e-05 | 0.00641984 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401262 | AACTTTTAATGTGCT[C/T]CCATAAGTTTGTTGT | 51455 |
| rs762087535 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482058 | TGGCCATGCTGGAAA[C/T]GCCAACCATGTGAAT | 51455 |
| rs762089403 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415679 | AACTCATATTGTACT[A/G]GCTTCACTTGGCTAC | 51455 |
| rs762123691 | snp | A/C | 1.89392e-05 | 0.00307721 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439315 | CGATGTGATTTCTAA[A/C]GCAGGAAAAAATTTT | 51455 |
| rs762166919 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468778 | ACATGAATGCAAAAG[C/T]ACCCTTACCCTTAAC | 51455 |
| rs762206227 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436471 | TGAGCTGTGATTCTG[C/T]CTCAAGCAGTCTGAT | 51455 |
| rs762230917 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415805 | CAAACCTAGCAAAGG[C/T]TGAATGAGGTGCAGA | 51455 |
| rs762241664 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400843 | TCAGGAATTTCAGAG[C/T]TTAGCAGTCTGGCCT | 51455 |
| rs762242149 | in-del | -/AG | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400195 | GCACCTGGTAACAGT[-/AG]AGATTTTTATACATT | 51455 |
| rs762267317 | in-del | -/TTTAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99447153 | ATATGTAAAATGTTA[-/TTTAT]TTGACTTTTTTTTTT | 51455 |
| rs762287320 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452800 | AGTGGTATAAATACT[G/T]AAAATCTCAAAACAC | 51455 |
| rs762296305 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99421879 | GCATATTGGATAGGA[A/G]AATGTTTGAGGAGTA | 51455 |
| rs762318027 | snp | C/G | 1.65113e-05 | 0.00287322 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439180 | GCGGAATTCCATTCT[C/G]TTTCCTTCCCGGAGA | 51455 |
| rs762327966 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480803 | AGCAGAAGTTGTCAC[G/T]GCTTCTGGAATTTTC | 51455 |
| rs762376327 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406396 | CGGACAGAGTATGAC[C/T]CACTAGGAAAGTGGC | 51455 |
| rs762444221 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461827 | TCAAAAGTGGATGTG[C/T]GGATAAATTCATCCT | 51455 |
| rs762464459 | snp | C/T | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412885 | TTTGCCATGGTCATA[C/T]ACTGCAAGTCTCCAC | 51455 |
| rs762467750 | snp | C/G | | | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400469 | AGTTCCAAATATCCA[C/G]TAGCATAGAATTTTA | 51455 |
| rs762479536 | in-del | -/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480764 | TGCTTCTATTAAATG[-/T]TAATTCCAAATAAAC | 51455 |
| rs762490812 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447877 | AGGCACAAGCCACCA[C/G]TCCCAGCTAATTGTA | 51455 |
| rs762504516 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412780 | GAAACAGATTTTCTT[C/T]CCTTTTCAGTTCGAA | 51455 |
| rs762506560 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459261 | TCTGTATATTAACTG[-/T]TATCAGTATCAATTT | 51455 |
| rs762551904 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484141 | AGAACACCAAACACC[A/G]CATGTTCTCACTTGC | 51455 |
| rs762552827 | snp | G/T | 1.651e-05 | 0.0028731 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405948 | TACTCAGGTTAAGTC[G/T]CGACTGCACACTGAC | 51455 |
| rs762577592 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99420493 | TGCCTTGCCTTTCTG[A/G]AAAAAACCCTAACAA | 51455 |
| rs762580329 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433030 | AAGATGCTACTGCAA[C/G]TATATACATGGTGGT | 51455 |
| rs762585153 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415505 | AATAAAGTTTTCACC[A/G]TCTACAGGAGTGCTG | 51455 |
| rs762592721 | snp | C/G | 1.68932e-05 | 0.00290625 | intron-variant | REV1 | GRCh38.p7 | 2:99434476 | TATTAAATTATTTCT[C/G]TATGTGGTACAGGAA | 51455 |
| rs762641340 | snp | A/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482572 | GCAGGTGCCCAAATT[A/T]CACTACAGCTATAAA | 51455 |
| rs762652123 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463130 | AATACATAAAACACA[C/T]AGGTCAAAGAAGAAT | 51455 |
| rs762660729 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428308 | AAAGAGACTAGCCTA[C/T]TGAGCACAACATAAA | 51455 |
| rs762667379 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430342 | TGGGGAAAAGTTAAC[A/G]AAAAATATAAATTTC | 51455 |
| rs762667691 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407312 | TCCCAGCACTTTGAG[A/G]GGCTGAGGTGGGTGG | 51455 |
| rs762670008 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434585 | TAATCCTTAAAGAAG[C/T]TAATACTTTAAAGAT | 51455 |
| rs762680942 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456188 | GTGAAAATATTTTAA[C/T]ATTCTGATGTACAAA | 51455 |
| rs762698289 | in-del | -/CAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99416912 | AGCAAGACTCCATCT[-/CAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs762742154 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462018 | TTTACTTCCTAAACT[C/G]TGAGAATTCAGGTCC | 51455 |
| rs762762813 | snp | C/T | 1.66247e-05 | 0.00288307 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408130 | GGTCAAGAGTTACAG[C/T]CCTGTAAGTGATAGA | 51455 |
| rs762783858 | snp | A/G | 1.65119e-05 | 0.00287327 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438937 | AAGAATTAGTTCTGT[A/G]TGGATTCCGCAAAGC | 51455 |
| rs762807822 | in-del | -/A | 3.47228e-05 | 0.00416656 | intron-variant | REV1 | GRCh38.p7 | 2:99405899 | TATATTTAGGACTAC[-/A]AAAAATGTACCTGGG | 51455 |
| rs762820662 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99421390 | AGCAATGCTAAAAAC[A/G]GTTTTACAAGTGAGA | 51455 |
| rs762850171 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99428991 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51455 |
| rs762864054 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99457011 | ATTTGGAAAATGCCT[A/G]TTTATCTAAGACCAA | 51455 |
| rs762870514 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99444463 | TGGTCAGCACTGATC[A/G]TATACAAGGGTGTCA | 51455 |
| rs762896367 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491856 | CTTGAGCCAACTGAC[C/T]TTGGCAATACCTTTA | 51455 |
| rs762906631 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99408466 | TATTTTCCAGCTAAA[A/G]CACAAGTGAATGGTA | 51455 |
| rs762914438 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469073 | ATCTATAAAACAAAG[C/T]TCGACTGCAGAATCT | 51455 |
| rs762927409 | in-del | -/GAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99405183 | AAGCTGAATTTTCTC[-/GAA]TAACTTACAGGACAG | 51455 |
| rs762929287 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443165 | TATATGGCTACTCTA[C/T]CTTTAAAATTATCAT | 51455 |
| rs762960882 | snp | A/C | | | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402596 | TGTTCTCAAATCATG[A/C]GACGACTACATCTCA | 51455 |
| rs763017016 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428564 | ACGTTTGAACTTAAT[A/G]CTTTTTAACTTAAAT | 51455 |
| rs763046340 | snp | C/T | 8.24151e-05 | 0.00641878 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402758 | GGTCAGACTGCAAAC[C/T]AGAAAGGCCTGGCAC | 51455 |
| rs763083123 | snp | G/T | 1.64863e-05 | 0.00287104 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435897 | CCATATCAACATGCA[G/T]TATACAGCTCTGATG | 51455 |
| rs763086864 | snp | C/T | 1.65416e-05 | 0.00287586 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449357 | ACAATCCATTCTGGT[C/T]GAATTACTTTTTCCC | 51455 |
| rs763127237 | snp | A/G | 1.66977e-05 | 0.00288939 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410718 | GTTATCACAAATTCC[A/G]TGGCCTCCAAATTTT | 51455 |
| rs763132684 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99467339 | GACAAATGTTTAAAA[C/T]TTTAAAAGGAAAAGG | 51455 |
| rs763151766 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99451283 | ACGGCTGTCCTTTAC[C/T]GAATAAAAAGACACG | 51455 |
| rs763192452 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468755 | TAAAAAACGGATGAA[A/G]AGTGAATACATGAAT | 51455 |
| rs763206693 | snp | A/G | 1.69092e-05 | 0.00290763 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403809 | CAGCAAATACCTCAG[A/G]GTCCACCTAGTGGAA | 51455 |
| rs763262673 | snp | A/G | 3.29663e-05 | 0.00405981 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406382 | CTTGGAAGACATCAC[A/G]GACAGAGTATGACCC | 51455 |
| rs763266927 | snp | C/T | 1.65206e-05 | 0.00287403 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439166 | GCTCCCTCTGGGATG[C/T]GGAATTCCATTCTGT | 51455 |
| rs763282091 | snp | A/G | 1.65105e-05 | 0.00287315 | intron-variant | REV1 | GRCh38.p7 | 2:99442472 | TCCAGCTTTGATGCT[A/G]AAACAAAAAGCAACA | 51455 |
| rs763297945 | snp | A/G | | | intron-variant, upstream-variant-2KB, missense | REV1 | GRCh38.p7 | 2:99479692 | AGTCAGGAGGCTGAG[A/G]TGGGAGGATCGCTTG | 51455 |
| rs763314259 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452926 | TTTGCTAGTTACTTG[G/T]ATTTCAGGCAAGTTA | 51455 |
| rs763322886 | snp | C/G | 1.71009e-05 | 0.00292406 | intron-variant | REV1 | GRCh38.p7 | 2:99406293 | AGGACATAAGCAGCA[C/G]CTAAAAAAGAACCAC | 51455 |
| rs763323821 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99402122 | ATGGCAAAATAAAGG[A/G]TATCACTTTCTCATT | 51455 |
| rs763325484 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416565 | CCCTATCTTTCAAAT[C/G]TCCCTTAGGAAATTC | 51455 |
| rs763362724 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99441488 | AAAAAAGCAGCCACA[C/T]GGAATAGTCTAGATT | 51455 |
| rs763421986 | snp | A/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439592 | TTTTTGTTTGTTTTT[A/T]ATTTTCACTTCAGAT | 51455 |
| rs763464072 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99423373 | CATCCAGTAAATGCA[C/T]TTTTACTGGAACTAC | 51455 |
| rs763467666 | snp | C/T | 1.65597e-05 | 0.00287743 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401232 | GAGCATCAGGCTCTC[C/T]GGTAATATTTATGTA | 51455 |
| rs763508671 | snp | A/C/T | 3.35189e-05 | 0.00409372 | intron-variant | REV1 | GRCh38.p7 | 2:99418993 | GTCACAATTATTTTT[A/C/T]AAATTTCTCAACAAA | 51455 |
| rs763511725 | snp | A/G | 0.000133932 | 0.00818217 | intron-variant | REV1 | GRCh38.p7 | 2:99424947 | GTCTCAGTGCCCCAC[A/G]TTACCTTTGACATTT | 51455 |
| rs763520512 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460637 | TATCTATAAAGTGGT[A/G]AAGTATTCACTAAAA | 51455 |
| rs763569915 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99473676 | TACTGAAACATTTTC[C/T]TGTTGCTAATTTTTT | 51455 |
| rs763578064 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444881 | AAGGAACTGTACTGA[C/T]ATTTTCTACTATTCT | 51455 |
| rs763610053 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99459826 | ACAGGTGAACTATTA[C/G]AGGGTCTTCCCTCCA | 51455 |
| rs763612257 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456840 | TGAGGAGGGAAGGAG[-/T]TTTTCCTCAGAGGCA | 51455 |
| rs763648453 | snp | A/G | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402282 | ATCCAGTTTTTCCAA[A/G]TCTTTTTCTTCTATT | 51455 |
| rs763650834 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99408923 | TCCCAGAAAAAATTA[C/T]TATAAATTGAATTGG | 51455 |
| rs763665746 | in-del | -/AAG | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433179 | CACAGAAAATACAAA[-/AAG]AAAAACCAACCTACC | 51455 |
| rs763708621 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428518 | AGTTTGGCATGTCAT[A/G]AATGGAAAACAGTTT | 51455 |
| rs763736642 | snp | C/T | 5.02803e-05 | 0.00501374 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402610 | GAGACGACTACATCT[C/T]AGCCTTGGGCCATCT | 51455 |
| rs763739494 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430423 | CTAACTAACGGGTAC[A/G]ACAAACATGAAATTC | 51455 |
| rs763740232 | in-del | -/T | 1.64876e-05 | 0.00287116 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449427 | CAATAATATGTGTTG[-/T]TTTAGATCTGGAATA | 51455 |
| rs763748143 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430618 | GATCAGAGTATCGAT[A/G]CTTTAGAGAACACAA | 51455 |
| rs763755012 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99469971 | CTAAAAATACAAAAA[A/G]TTAGCCGGGCATGGT | 51455 |
| rs763773662 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463133 | ACATAAAACACATAG[G/T]TCAAAGAAGAATTTT | 51455 |
| rs763838153 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99431523 | AAGCTTGAACAGCCA[C/T]AACCAACTGTCTTTC | 51455 |
| rs763847299 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482694 | CGTTGTGTTTGCTTC[A/G]GCTGCACATACACTA | 51455 |
| rs763850555 | snp | C/T | 1.67248e-05 | 0.00289173 | intron-variant | REV1 | GRCh38.p7 | 2:99408142 | CAGTCCTGTAAGTGA[C/T]AGAATTAAAAAACAA | 51455 |
| rs763860295 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476757 | GACCAAGTCCCAGTA[C/T]AAATGCTGGACACCA | 51455 |
| rs763876604 | snp | A/G | 4.9498e-05 | 0.00497459 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424250 | TTGTTTAGCATGCCC[A/G]AAAAACATTCCGTTC | 51455 |
| rs763917776 | snp | G/T | | | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405968 | TGCACACTGACAGGA[G/T]TATGTAGACCATTCC | 51455 |
| rs763928225 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99417085 | CTAAACTGTGTCTTC[A/C]CCAAATTTATATGCT | 51455 |
| rs763937824 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99404240 | CCCGTCTCTTCCCTG[C/G]TGCTTCAGCGGGAGG | 51455 |
| rs763940332 | snp | C/T | 1.66405e-05 | 0.00288443 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410722 | TCACAAATTCCATGG[C/T]CTCCAAATTTTGCAG | 51455 |
| rs763940467 | snp | A/G | 1.69444e-05 | 0.00291066 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403810 | AGCAAATACCTCAGG[A/G]TCCACCTAGTGGAAA | 51455 |
| rs763944918 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99469109 | GGGCCATGACTGGAT[A/G]AAGGGTGGATATGGT | 51455 |
| rs763963947 | snp | C/T | 0.000346069 | 0.0131497 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442344 | AGCTGTTTGGCTATA[C/T]TGCTTGGACCTGGCA | 51455 |
| rs764000189 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99454551 | GTGAAACTCCAGCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs764018095 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99418416 | AAGTACTTGTTTAAT[A/G]AACTCAGAAAACTGT | 51455 |
| rs764028215 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99445263 | AAACCAAAGTTTTGA[C/G]TCATATGTAAGCACA | 51455 |
| rs764032690 | snp | A/T | 1.651e-05 | 0.0028731 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438941 | ATTAGTTCTGTGTGG[A/T]TTCCGCAAAGCATCT | 51455 |
| rs764042344 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99474837 | AACGCGGTAGGCAGA[A/G]GTTGCAATGAGCCGA | 51455 |
| rs764068278 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99471516 | GACACTGGATTTTGC[-/A]ATGACTTTTTGGGGA | 51455 |
| rs764127786 | snp | C/T | 0.000122527 | 0.00782613 | intron-variant, stop-gained | REV1 | GRCh38.p7 | 2:99424773 | TACTCATCCTATTAC[C/T]ACCCAATTCCCAATT | 51455 |
| rs764132593 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488729 | GCTGATTTGCTACAT[A/T]CAGAACTCCATAGAA | 51455 |
| rs764149734 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99454862 | CAGACAATTGAAAGC[A/G]CAGTAAAAGTAAAAG | 51455 |
| rs764155083 | snp | A/G | 1.65419e-05 | 0.00287588 | intron-variant | REV1 | GRCh38.p7 | 2:99442490 | ACAAAAAGCAACACC[A/G]ATTTAGAGTTCCATA | 51455 |
| rs764179061 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99405454 | ATAGCTTAAGGTGCT[A/G]CCTTACTTTCAAGGA | 51455 |
| rs764185524 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99465345 | TAAGACAATCTAACA[A/G]AACATTTCCCTTCAT | 51455 |
| rs764264183 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461631 | AAATGATAAGAAGAA[G/T]AATCCCCAAGAAAAT | 51455 |
| rs764318798 | snp | A/C | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402950 | ATTAACTTCTGGGGA[A/C]TGCCACAGGCCCCTG | 51455 |
| rs764321126 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468773 | TGAATACATGAATGC[A/T]AAAGTACCCTTACCC | 51455 |
| rs764328008 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99441292 | TGATACTGGATCCTC[C/T]CAGATTAATTAGACT | 51455 |
| rs764341324 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448137 | ATTTATGCGGCTAAA[C/T]ACACTATACAAAGGA | 51455 |
| rs764374662 | in-del | -/A | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439686 | AGTTATTTTTCCCAT[-/A]AAAAAATTAATTGGA | 51455 |
| rs764423716 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463127 | ATAAATACATAAAAC[A/G]CATAGGTCAAAGAAG | 51455 |
| rs764429918 | snp | G/T | 4.94588e-05 | 0.00497262 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435898 | CATATCAACATGCAT[G/T]ATACAGCTCTGATGT | 51455 |
| rs764498977 | snp | C/T | | | intron-variant, upstream-variant-2KB, synonymous-codon | REV1 | GRCh38.p7 | 2:99479702 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGAAG | 51455 |
| rs764510396 | snp | G/T | 1.65138e-05 | 0.00287343 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439168 | TCCCTCTGGGATGCG[G/T]AATTCCATTCTGTTT | 51455 |
| rs764516976 | snp | C/G | 1.70872e-05 | 0.00292289 | intron-variant | REV1 | GRCh38.p7 | 2:99406294 | GGACATAAGCAGCAC[C/G]TAAAAAAGAACCACA | 51455 |
| rs764535843 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480850 | AATATATTTAAAATT[A/C]TATACTTTTAAAAAA | 51455 |
| rs764554128 | in-del | -/CTAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99414237 | TCAGTAGCAGAAAAA[-/CTAT]CTAGTCCAAGTTCTG | 51455 |
| rs764557108 | snp | C/T | 1.71284e-05 | 0.00292642 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403042 | TGAACCAATGGTTTT[C/T]TTCTTCTTGTTTCTT | 51455 |
| rs764557609 | snp | A/G | 3.30186e-05 | 0.00406303 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439061 | GGCTGGAGAAAGCCT[A/G]CTGGCAACACTGTTG | 51455 |
| rs764561539 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413938 | AATACTTTGGGAGGC[C/T]AACAGTCTGAGTTTG | 51455 |
| rs764568463 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400796 | AAGCTTTACCCTTTC[C/T]TGGAACAAGTAGAAT | 51455 |
| rs764584016 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99449014 | AATAGAAAGGCCATG[A/C]GCAGTGGTTGTAGTC | 51455 |
| rs764587002 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478598 | GTTGCAATAAATCAG[A/G]GATTCCAAAGGCCAC | 51455 |
| rs764602792 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99411013 | GAAACGTGGCCAGGC[A/G]CGGTGGCTCACACCT | 51455 |
| rs764612420 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454423 | GATGTGGTGGCATGC[G/T]CCTGTAACTCCAGCT | 51455 |
| rs764635157 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412771 | ATCTCAGCTGAAACA[A/G]ATTTTCTTTCCTTTT | 51455 |
| rs764637127 | in-del | -/AAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99454558 | TCCAGCTCAAAAAAA[-/AAAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs764637331 | snp | A/T | 1.64806e-05 | 0.00287054 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462497 | AAAAAGTACTCAACC[A/T]GTGTATCCATTAACA | 51455 |
| rs764674667 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434830 | ATTTCTAGAGTTAAC[A/T]TCTATACTTATCTCT | 51455 |
| rs764716464 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99431636 | GTCTTGAAAATAACA[C/G]AAAACTTATGCTTGA | 51455 |
| rs764733824 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99413328 | GTGTGACTTACAGAC[A/T]TACTAACCAACTCAC | 51455 |
| rs764800195 | snp | G/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482481 | GCAAGTCCTGGAGTT[G/T]GTAGCTAATATAAGA | 51455 |
| rs764812162 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447093 | CAGTGGGATGTTATA[C/G]GGACGAGCCTTTGAC | 51455 |
| rs764822267 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404623 | GGACAGCACAGACTT[C/G]CTCTACTTGTTCCCG | 51455 |
| rs764824876 | snp | A/G | 1.65151e-05 | 0.00287355 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434363 | GATTTTATTCTGGTA[A/G]TACTGCCACTCCAGC | 51455 |
| rs764873447 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99437700 | AACTAATTAATCATA[-/G]TTCTTAGAAGCATTA | 51455 |
| rs764877066 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426978 | TCACGAGGTCAGGAG[-/T]TCAAGACCAGCCTGG | 51455 |
| rs764882809 | snp | A/G | 2.65284e-05 | 0.00364191 | intron-variant | REV1 | GRCh38.p7 | 2:99429979 | AAAATTAATGGTTAT[A/G]TGTTATAAACTGATT | 51455 |
| rs764891967 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481140 | CAACCCTAACACAAA[C/T]AGATTATCAATGCCT | 51455 |
| rs764910142 | snp | G/T | 1.89288e-05 | 0.00307637 | intron-variant | REV1 | GRCh38.p7 | 2:99405869 | TGTATTTATATTTAG[G/T]AGTATAAAATGTACT | 51455 |
| rs765001264 | snp | A/C | 5.80501e-05 | 0.00538718 | intron-variant | REV1 | GRCh38.p7 | 2:99406540 | AACTAAAGTGAAAAT[A/C]TGAATTCAGCTAAGC | 51455 |
| rs765011251 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456154 | CCATTCCTTAAGACT[A/G]AGTTGATTTAGCATC | 51455 |
| rs765032908 | in-del | -/GACA | | | intron-variant | REV1 | GRCh38.p7 | 2:99458729 | CAATTTTGATGACCT[-/GACA]GATAATTTATGCTCA | 51455 |
| rs765034606 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99418776 | ATATTATAGATATGA[A/G]AAGTACTTGTAATGC | 51455 |
| rs765046465 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99442131 | GTGGCACACGCCTGT[-/A]AGCCTAGCTACTCGG | 51455 |
| rs765060826 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99454980 | TCAAAACAGCCATAT[A/G]AAGACCACTTTCACG | 51455 |
| rs765072342 | snp | C/T | 1.70927e-05 | 0.00292336 | intron-variant | REV1 | GRCh38.p7 | 2:99424329 | CTAGGAAGTTTTCAA[C/T]TCAAATATTTATCAA | 51455 |
| rs765082115 | snp | A/C | 3.36417e-05 | 0.00410119 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402593 | TTATGTTCTCAAATC[A/C]TGAGACGACTACATC | 51455 |
| rs765100551 | in-del | -/ACAG | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400051 | CTACCAATAAAGAAA[-/ACAG]ACAGACATCCACCAG | 51455 |
| rs765101301 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99441556 | TTCCATTTATATATT[C/T]ACATATTTAGAATGT | 51455 |
| rs765107259 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99468775 | AATACATGAATGCAA[A/G]AGTACCCTTACCCTT | 51455 |
| rs765151032 | snp | C/G | 1.6489e-05 | 0.00287128 | intron-variant | REV1 | GRCh38.p7 | 2:99462645 | TAAAGAAAAGGTAAA[C/G]CAATCACAAAGGTTA | 51455 |
| rs765154230 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99407253 | CACCACCACACCCGG[A/C]TAATTTTTGTATTTT | 51455 |
| rs765180664 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438839 | AGATACTGAAGAAGT[A/G]CTTTTTGTGCTTGAA | 51455 |
| rs765180719 | snp | A/C | 1.6669e-05 | 0.00288691 | intron-variant | REV1 | GRCh38.p7 | 2:99421679 | AGAGCAAAGGCAACG[A/C]ATCACAGCCACAGCC | 51455 |
| rs765183108 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486642 | TACAGATGAGCAGAA[C/T]TGAGGCACCACCAAG | 51455 |
| rs765224843 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488289 | TGTAGTGATCTTATA[A/T]ATTCAAGCACATTAT | 51455 |
| rs765249870 | in-del | -/A | 1.65392e-05 | 0.00287564 | intron-variant | REV1 | GRCh38.p7 | 2:99404682 | GACTGATCCAGCTAT[-/A]AAATGCCAAACATAT | 51455 |
| rs765274552 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418481 | GCTCAAAACTTTTAT[C/T]TTTAGCCCAGGAGTA | 51455 |
| rs765274982 | in-del | -/CAAC | | | intron-variant | REV1 | GRCh38.p7 | 2:99477191 | AGGAGGCAGAGTGGG[-/CAAC]CAGAGACTACATTTC | 51455 |
| rs765301518 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99466874 | TGCTCTGTTAAATAT[A/T]TCTCCTGTTTTCAAG | 51455 |
| rs765322849 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99442999 | CACACAACACCACTC[A/G]AATCCAGGGGAACAC | 51455 |
| rs765353402 | snp | A/T | 1.75207e-05 | 0.00295973 | intron-variant | REV1 | GRCh38.p7 | 2:99435796 | ATATATTTATAACAA[A/T]ATATCAGTTTTCTTA | 51455 |
| rs765390667 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99485280 | TATTACAAAGTCACT[A/G]TCTCCATCAATTCTT | 51455 |
| rs765393483 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99479586 | GGGAAGATCTCTTGC[A/G]TGAGACCAGCCTGAG | 51455 |
| rs765400663 | snp | C/G | 4.94352e-05 | 0.00497143 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442445 | CTGATATGGAATGTA[C/G]GAGAGGAGTCGTCCA | 51455 |
| rs765459821 | snp | A/G | 0.00026431 | 0.0114928 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412931 | AAGATGCCAACTTAG[A/G]TTCCATTGAATGTCC | 51455 |
| rs765461952 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | REV1 | GRCh38.p7 | 2:99400905 | AGTAGTTGCTTCCTA[C/G]AGTTGAGTTTTTAAG | 51455 |
| rs765467752 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99449208 | AGGTTGAGGCTGCAG[C/T]GAGCCATGATCATGC | 51455 |
| rs765517314 | snp | C/G | 0.000164987 | 0.00908108 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438976 | TTCTGGTGCTTTGCT[C/G]CAACTGCTGCAGAGT | 51455 |
| rs765554520 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414289 | CCAGTATATAACACA[A/G]GGTTAGGAAGTCATC | 51455 |
| rs765596759 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478205 | TCACACCACTGCACT[A/G]GCCAACACTGAGACT | 51455 |
| rs765659673 | snp | C/T | 1.71578e-05 | 0.00292893 | intron-variant | REV1 | GRCh38.p7 | 2:99406282 | CCGTCTTTCCAAGGA[C/T]ATAAGCAGCACCTAA | 51455 |
| rs765664269 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462863 | GAAGCTGAGGCAGGC[A/G]GATCACCTGAGATCA | 51455 |
| rs765666425 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99401993 | CCCACCCCAGCCTCC[C/T]GAAGTGAAGTACAGG | 51455 |
| rs765691271 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436802 | AAATCCTGGAAAAAG[A/T]ACCCTGGGCTTGTAA | 51455 |
| rs765693480 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418831 | ATTTCTATTTACCTG[A/G]TAGATTGGTCACTAG | 51455 |
| rs765707248 | snp | A/G | 1.64874e-05 | 0.00287113 | stop-gained, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410762 | GAGCCCCAGGCTTTC[A/G]TACCATGATTTTGAG | 51455 |
| rs765707597 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99459738 | AAAACAAACAAAAAG[A/G]ATAGAAGGCAAAGAA | 51455 |
| rs765719810 | in-del | -/CAAT | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483953 | GAGGTGTTGAGAAGC[-/CAAT]AACTCATAATTTAGA | 51455 |
| rs765782866 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422029 | TGAATTTGAACTGTC[A/T]AAACATTTAATCTAA | 51455 |
| rs765953652 | snp | A/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433080 | TTTAGTATTTCATAA[A/T]TGCCTAATATATGAC | 51455 |
| rs765955818 | snp | A/G/T | 5.25255e-05 | 0.0051245 | intron-variant | REV1 | GRCh38.p7 | 2:99429977 | AAAAAATTAATGGTT[A/G/T]TATGTTATAAACTGA | 51455 |
| rs765956055 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410768 | CAGGCTTTCGTACCA[C/T]GATTTTGAGAGTTAG | 51455 |
| rs765985827 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460970 | CCTATGTGAATAAGG[A/G]TGCTCTCTTGAACTG | 51455 |
| rs766000454 | snp | A/G | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439047 | TCCTCCTGGGAAAAG[A/G]CTGGAGAAAGCCTGC | 51455 |
| rs766021854 | in-del | -/AG | | | intron-variant | REV1 | GRCh38.p7 | 2:99447181 | TTTTTTTTTTTAGAC[-/AG]AGTCTCACTTTGTCG | 51455 |
| rs766039327 | snp | A/G | 3.43719e-05 | 0.00414545 | intron-variant | REV1 | GRCh38.p7 | 2:99404725 | AAAGCATGCTCAGAG[A/G]TGAGGTGTTTGGGAG | 51455 |
| rs766040882 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99434780 | CTAGATTCAGACTTA[A/C]GTAGTGGGGAAAGAA | 51455 |
| rs766046142 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456252 | AATACTTATTGAGTA[C/T]CTACAATGTGCCAGG | 51455 |
| rs766046622 | snp | A/T | 1.74449e-05 | 0.00295332 | intron-variant | REV1 | GRCh38.p7 | 2:99410900 | TGGAGAAACTACCAT[A/T]CCACTTTCCTATATA | 51455 |
| rs766053518 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472755 | ACAAGAACCAGGTAT[C/T]GCCTTTATGAGTGAC | 51455 |
| rs766072171 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99474327 | AAAAGTTCTGTAAGG[C/T]TGCACTGCTGGCTTG | 51455 |
| rs766124020 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487992 | AGGTGGGAAATGGTA[A/T]CTTCATTCTACAAAC | 51455 |
| rs766124807 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99408532 | TTCCAAGATTATGTA[C/T]GCTGAGGTATAGCAA | 51455 |
| rs766131251 | snp | A/T | 8.56274e-05 | 0.00654266 | intron-variant | REV1 | GRCh38.p7 | 2:99402218 | ATGCCATTTTTTCCC[A/T]TTTGATAAAAGTGAT | 51455 |
| rs766161358 | snp | C/T | 1.65935e-05 | 0.00288036 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429903 | TCAATTCCATTTGCT[C/T]GCGCAGAATCTGGAT | 51455 |
| rs766174901 | snp | A/C/T | 3.29588e-05 | 0.00405938 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421546 | TCTTTGATTTCCATA[A/C/T]GAACAGCATTTGCAA | 51455 |
| rs766241218 | snp | G/T | 1.65395e-05 | 0.00287567 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449484 | ACATCATTAGTTTTC[G/T]CAATTCCTCAGCGGA | 51455 |
| rs766294860 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99424467 | AGTCACAACTGTCTG[A/C]ATAGTGTAAATGACA | 51455 |
| rs766326747 | snp | C/T | 1.68789e-05 | 0.00290503 | intron-variant | REV1 | GRCh38.p7 | 2:99438594 | GACAATTTTAATAAG[C/T]ATCTACCTGTGTCAG | 51455 |
| rs766329854 | in-del | -/A | 4.9476e-05 | 0.00497348 | frameshift-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406018 | CTTGTTAGTATCAGG[-/A]CTGGTCGGCAGATGT | 51455 |
| rs766346710 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404598 | TTGTCGCCATGTGAC[A/T]CTGCTTGCTGGACAG | 51455 |
| rs766438799 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430186 | AGTGTCCTGGGAGGT[C/T]TGTTTTTTTTTTAAA | 51455 |
| rs766443724 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99418043 | ACCTACCATAAAATG[A/C]CATTTCTGTCGTTTA | 51455 |
| rs766449132 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444899 | TTTCTACTATTCTTT[C/T]AAAACCAAAAGGAGA | 51455 |
| rs766454670 | in-del | -/A | 0.000661178 | 0.0181701 | intron-variant | REV1 | GRCh38.p7 | 2:99429959 | ATCTGCTTTAAAAAT[-/A]AAAAAAAATTAATGG | 51455 |
| rs766461225 | snp | C/T | 1.66073e-05 | 0.00288156 | intron-variant | REV1 | GRCh38.p7 | 2:99406519 | TAAAGAGTATGCTTC[C/T]AGGAAAACTAAAGTG | 51455 |
| rs766513820 | snp | C/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406410 | CCCACTAGGAAAGTG[C/G]CTTGACTGAACTGAT | 51455 |
| rs766515088 | snp | C/T | 1.94392e-05 | 0.00311757 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403066 | GTTTCTTTTCTTTTC[C/T]TTCACTGCTGCCTTT | 51455 |
| rs766525326 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414423 | AGCCAGAACAAAGGG[C/G]AAGTAAATACCAAAG | 51455 |
| rs766526344 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452974 | TCAGTTTCCTCACAT[G/T]TAAACTGGGGATAAT | 51455 |
| rs766535632 | in-del | -/C | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491325 | AGTTTTGCTCTTTTG[-/C]CCAGGCTGGAGTGCA | 51455 |
| rs766615166 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401030 | CAAACATTTTGTAAA[C/T]AGAATCTATGCTACA | 51455 |
| rs766624399 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459618 | GCCTGAGGAGAGAGG[A/T]TGGCTTGAACCTGGG | 51455 |
| rs766627431 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463707 | TCAGCTCACTGCAAA[C/T]TCCGCCTCCCAGGTT | 51455 |
| rs766633103 | in-del | -/CTACAGGCG | | | intron-variant | REV1 | GRCh38.p7 | 2:99443956 | CCCGAGTAGCTGGGA[-/CTACAGGCG]CCTGCCACCACGCCC | 51455 |
| rs766635378 | snp | C/T | 0.000148306 | 0.00860993 | intron-variant | REV1 | GRCh38.p7 | 2:99403676 | TTCATTTTTGTTACA[C/T]GCCACTTCCAAGGCT | 51455 |
| rs766655273 | snp | A/G | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424181 | ATACAATGTTTGTGC[A/G]ACTTCCTTATATGCA | 51455 |
| rs766681885 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415961 | ATCATATTAAGAAAC[A/G]TATTTATTAGTGTAA | 51455 |
| rs766692043 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99457083 | CCCAAAGGCAATTGT[C/T]TCCTCTTCTGTGTTG | 51455 |
| rs766693137 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99438012 | TCTGTAAAAGGAACT[A/G]AAATTTCAAACCAGA | 51455 |
| rs766702730 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99465848 | GTCAAATCAGCTCTG[A/T]TATGATCTATGAGAA | 51455 |
| rs766709386 | snp | C/T | 1.65105e-05 | 0.00287315 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412926 | TCCCAAAGATGCCAA[C/T]TTAGATTCCATTGAA | 51455 |
| rs766715261 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477354 | CAGTTGTGAGGTAAC[C/T]CAGCTTCAACCATGG | 51455 |
| rs766724125 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99457465 | GGCAGGCAAATCACC[C/T]GAGGTCAGGAGTTCG | 51455 |
| rs766745375 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99458893 | AGTGGGTGTGACTAT[C/G]AAAGAGTAACATGAA | 51455 |
| rs766757640 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487462 | AGATAATGGAACTTA[C/G]ACTAGGATTCATGTA | 51455 |
| rs766793551 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405958 | AAGTCTCGACTGCAC[A/G]CTGACAGGAGTATGT | 51455 |
| rs766813125 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469864 | TTCATGTAAAAATGA[C/T]ATTTCCTAGCACTCT | 51455 |
| rs766827358 | snp | A/G | 1.70075e-05 | 0.00291607 | intron-variant | REV1 | GRCh38.p7 | 2:99434490 | TGTATGTGGTACAGG[A/G]ATGTTAACAACATGT | 51455 |
| rs766830184 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99436067 | AGTCTTTTTAAAAAA[A/C]CAGAATTGAGTACAG | 51455 |
| rs766835144 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470823 | GGTCTCCTTTGTTCG[G/T]TGTACTCTCATGGCA | 51455 |
| rs766874966 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425066 | ATTATAGTAAAAACA[A/G]GCAAAATAATAAAGC | 51455 |
| rs766896851 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436442 | TTAAGTCACATAGCC[C/T]ATTATTAAATGGTTG | 51455 |
| rs766909351 | snp | C/T | 0.000121219 | 0.00778428 | intron-variant, synonymous-codon, missense | REV1 | GRCh38.p7 | 2:99424845 | ATGCCAACAGCATTG[C/T]ACATGGTAGGACATC | 51455 |
| rs767089265 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99471201 | CTGTTTTCAGTGCCT[C/T]TTTATCTTACTTAGC | 51455 |
| rs767094051 | in-del | -/ATGAGGCAGGAGA | | | intron-variant | REV1 | GRCh38.p7 | 2:99485893 | GGATGAGGCAGGAGG[-/ATGAGGCAGGAGA]CTGTAGCCCAAGAGT | 51455 |
| rs767104692 | snp | G/T | 1.64985e-05 | 0.0028721 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439040 | CTTATCCTCCTCCTG[G/T]GAAAAGGCTGGAGAA | 51455 |
| rs767113494 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429885 | GCCCTTGACAAAACA[A/G]AATCAATTCCATTTG | 51455 |
| rs767141790 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99407623 | TGTTTCAAAGGCATC[C/T]TGATGTGCCTGTGGT | 51455 |
| rs767144464 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99405455 | TAGCTTAAGGTGCTA[C/T]CTTACTTTCAAGGAC | 51455 |
| rs767169436 | snp | C/G | 4.96882e-05 | 0.00498414 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406058 | GGTGGCAAGAAAGTG[C/G]AAGTTCTAGAAGCAG | 51455 |
| rs767173145 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484281 | TATTGTGTATCAGGC[C/T]TAATACCTGAGTGAT | 51455 |
| rs767175812 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99443407 | TTGACATTTTCATTT[C/T]CTTAAATGGTGTCAC | 51455 |
| rs767181996 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407675 | ATACAGCAGATGCAG[A/G]GTATGTTTCTGATTA | 51455 |
| rs767186933 | in-del | -/A | 1.6507e-05 | 0.00287284 | intron-variant | REV1 | GRCh38.p7 | 2:99435949 | ATATCTCCTAGAAGG[-/A]AAAAAGACAGCATTC | 51455 |
| rs767209154 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486091 | GATCACACCACTGCA[C/T]TCCAGCTTGGGCAAC | 51455 |
| rs767209369 | snp | G/T | 1.66765e-05 | 0.00288756 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402625 | CAGCCTTGGGCCATC[G/T]AACACAGGCCAAGCC | 51455 |
| rs767213843 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449455 | ATAATATACATGGTA[C/T]TGACCTCCATGCAAC | 51455 |
| rs767256742 | in-del | -/C | 0.000431329 | 0.0146792 | intron-variant | REV1 | GRCh38.p7 | 2:99442277 | AAAAAAAAAAAAAAA[-/C]CAACCAGCTTTGCAG | 51455 |
| rs767270258 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99408785 | AAACAGAATTACTAA[C/T]TCAGTAACAGATTAA | 51455 |
| rs767287347 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464662 | TTTTCTGTATTATTA[A/G]CAATGCTGCAATAAA | 51455 |
| rs767293680 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99421306 | GAAATATTCTAACTT[A/C]TTTATTGCGAAGATT | 51455 |
| rs767337091 | snp | C/T | 3.36661e-05 | 0.00410267 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401191 | TTTGCAAATACCTCA[C/T]AAGCACTTATGGCAC | 51455 |
| rs767356959 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415949 | TTAGGTAACCGGATC[A/G]TATTAAGAAACGTAT | 51455 |
| rs767414006 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99450520 | TATGACAATAATTAG[A/G]TGAGCTTTAGTTTCT | 51455 |
| rs767443078 | snp | A/G | | | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402457 | ATGTCACTAACAGCT[A/G]TCAAAGGAATGGGCT | 51455 |
| rs767504804 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419145 | AGAGGTTTCTCTTTG[C/T]TCTAACGCAAGTGCC | 51455 |
| rs767520708 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99487338 | AAAGTGACAATCTGA[-/TT]TACATTTTTAAAAAG | 51455 |
| rs767542367 | snp | A/T | 1.65567e-05 | 0.00287716 | intron-variant | REV1 | GRCh38.p7 | 2:99442499 | AACACCAATTTAGAG[A/T]TCCATACTTGGTGAC | 51455 |
| rs767581765 | snp | A/C | 1.73015e-05 | 0.00294116 | intron-variant | REV1 | GRCh38.p7 | 2:99438575 | CATGACTGTTTCTTA[A/C]GAAGACAATTTTAAT | 51455 |
| rs767606086 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99465778 | TAATTTTCTTCTAGT[-/A]ACTATATACATGTGT | 51455 |
| rs767670678 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99476845 | CCAGAAGTTGGCACC[A/G]TCCATAACTTCGCTG | 51455 |
| rs767671452 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403919 | AAATCTCACTTTTCT[A/G]ATCTGTACGAATTCT | 51455 |
| rs767676177 | in-del | -/CCC | 0.000100025 | 0.00707124 | intron-variant | REV1 | GRCh38.p7 | 2:99462669 | AAGGTTACATTTTCT[-/CCC]CCCTTTTTTGAAAAA | 51455 |
| rs767680746 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99453066 | AGTAACTTGCATATA[A/G]TAAAAATTATGTGGC | 51455 |
| rs767683665 | in-del | -/ACTT | 1.68243e-05 | 0.00290032 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401195 | AAATACCTCACAAGC[-/ACTT]ACTTATGGCACAGCT | 51455 |
| rs767710888 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401266 | TTTAATGTGCTTCCA[C/T]AAGTTTGTTGTAAAA | 51455 |
| rs767753945 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99457259 | AGAAAAATAAAATGG[A/G]ATATAAGGTCTGTAA | 51455 |
| rs767762920 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99475937 | GCAGCAAGCTGAGAT[A/C]ATGCCACTGCACTCC | 51455 |
| rs767769736 | in-del | -/AAT | | | intron-variant, upstream-variant-2KB, cds-indel | REV1 | GRCh38.p7 | 2:99481388 | AAATTATATTGTATC[-/AAT]AAAAAAAATGTTATG | 51455 |
| rs767770788 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454841 | AACTAAAACCAGACA[C/T]AGTGACAGACAATTG | 51455 |
| rs767808819 | in-del | -/A | | | intron-variant, upstream-variant-2KB, frameshift-variant | REV1 | GRCh38.p7 | 2:99479946 | GTAGGATTTTACAGG[-/A]ATAGAAGGTAGGATA | 51455 |
| rs767821972 | in-del | -/AACT | | | intron-variant | REV1 | GRCh38.p7 | 2:99431527 | TGAACAGCCACAACC[-/AACT]AACTGTCTTTCCAAG | 51455 |
| rs767840556 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434382 | TGCCACTCCAGCTGG[A/G]GGTTAGCGCCAGGAC | 51455 |
| rs767915794 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411282 | GACAGAGGGAGACTC[C/T]GTCTCAAAAAAGTAA | 51455 |
| rs767919665 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480843 | CACCAAGAATATATT[C/T]AAAATTATATACTTT | 51455 |
| rs767923457 | snp | G/T | 3.67148e-05 | 0.00428439 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403056 | TTTTCTTCTTGTTTC[G/T]TTTCTTTTCTTTCAC | 51455 |
| rs767932315 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99468786 | GCAAAAGTACCCTTA[A/C]CCTTAACATTTAGGG | 51455 |
| rs767978619 | snp | C/G/T | 3.29621e-05 | 0.00405958 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412787 | ATTTTCTTTCCTTTT[C/G/T]AGTTCGAACTGGTCT | 51455 |
| rs767979357 | in-del | -/AA | | | downstream-variant-500B | REV1, EIF5B | GRCh38.p7 | 2:99400449 | GGTGTTTGTTTGAGG[-/AA]AAAAAGTTCCAAATA | 51455 |
| rs768005798 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99412557 | CAGTCTCAGTCTTAT[C/T]TGGGGCTACACCTTA | 51455 |
| rs768016595 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415845 | ATTGAAGAGTGCATG[C/T]GCAGGTAAAAAGCCC | 51455 |
| rs768030649 | snp | C/T | 3.03255e-05 | 0.00389382 | intron-variant | REV1 | GRCh38.p7 | 2:99429989 | GTTATATGTTATAAA[C/T]TGATTTTCCCTCACT | 51455 |
| rs768080522 | in-del | -/TA | | | intron-variant | REV1 | GRCh38.p7 | 2:99422515 | TCAGATTAAGATCTC[-/TA]TTAAAGAAATAATCT | 51455 |
| rs768084439 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483969 | AATAACTCATAATTT[A/G]GATATTCTTACAAAT | 51455 |
| rs768110261 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439474 | AAAAAAACCCTGAAA[C/T]TTAAACCACAAACTT | 51455 |
| rs768133986 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466134 | TTTTTTGTATTTTTA[A/G]TAGAGACGGCGTTTC | 51455 |
| rs768155893 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447918 | AGACAGGGTTTCACC[A/G]TGTTGGCCAAGCTGG | 51455 |
| rs768166165 | snp | A/T | 1.66713e-05 | 0.0028871 | intron-variant | REV1 | GRCh38.p7 | 2:99418799 | TGTAATGCCTGTAAT[A/T]AAAGTATTGTTAAAA | 51455 |
| rs768183034 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99425990 | GCAGTGAGCCGAGAT[C/G]GCGCCATTACACTCC | 51455 |
| rs768220157 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478833 | TTTGCATTTCCAGCT[A/G]GACTGCGGCACACAC | 51455 |
| rs768231026 | in-del | -/GTAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99460635 | TTTATCTATAAAGTG[-/GTAAA]GTATTCACTAAAACT | 51455 |
| rs768247744 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99485622 | GCCACTCTGGTGGGC[A/G]GTTGTTGAGATAATC | 51455 |
| rs768254166 | snp | A/C | | | intron-variant, missense, stop-gained | REV1 | GRCh38.p7 | 2:99424816 | GCTCCTGAAGTGGCT[A/C]CACAGTGGTTGAGAT | 51455 |
| rs768276863 | in-del | -/CT | | | intron-variant | REV1 | GRCh38.p7 | 2:99435669 | AGGGAGAAAGAAAAA[-/CT]CTAATTTCCCTATAC | 51455 |
| rs768302521 | snp | G/T | 3.2987e-05 | 0.00406108 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435846 | GACCTTTGAGATCTG[G/T]TCTATTTCGTATACC | 51455 |
| rs768415552 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99459311 | GCAAGTTTATTACAT[A/G]TTACCATTTGGGGAA | 51455 |
| rs768475214 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477920 | AGAAAGGGAAAGAAG[G/T]AGAGACACTGTTTTA | 51455 |
| rs768488502 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432574 | GGTGAGCTCCTAATA[C/T]GTGAAAAGGCTTAGG | 51455 |
| rs768497245 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | REV1 | GRCh38.p7 | 2:99402864 | GTATATTAAGATCTC[A/G]TAAAGGTCAAAGTTA | 51455 |
| rs768510284 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439018 | AATCAGTGCTGCTCT[C/T]CTCAGCCTTATCCTC | 51455 |
| rs768512400 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99458362 | AACATTATTAGCCAC[A/G]AGGCAAATGCAAATT | 51455 |
| rs768565185 | snp | A/T | 2.16036e-05 | 0.00328654 | intron-variant | REV1 | GRCh38.p7 | 2:99429959 | ATCTGCTTTAAAAAT[A/T]AAAAAAAATTAATGG | 51455 |
| rs768592498 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402981 | GCAGAGTTTTTGCAG[C/G]ACTGTTAAGCAGCTT | 51455 |
| rs768643407 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456211 | TGTACAAATACAAAA[C/G]CTGTTATTTATTTAT | 51455 |
| rs768667488 | snp | A/G | 1.6546e-05 | 0.00287624 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401234 | GCATCAGGCTCTCTG[A/G]TAATATTTATGTAAC | 51455 |
| rs768678862 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404566 | CTGTATTACAGCCAT[G/T]TACTGGTTCTTTCTT | 51455 |
| rs768680906 | snp | G/T | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412742 | GTACCTGAGTAAACC[G/T]TATTCCATAGTTGAT | 51455 |
| rs768683447 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99437836 | CTAAAAGCACATAGG[A/G]ATACATCAAACTCAG | 51455 |
| rs768692862 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400115 | AGCTTCTCTCCCACA[A/G]GTTGTCCTCCTAGGA | 51455 |
| rs768700985 | snp | C/G | 3.29707e-05 | 0.00406008 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402764 | ACTGCAAACTAGAAA[C/G]GCCTGGCACACCTGA | 51455 |
| rs768707379 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470588 | AAGCAAGCGTTAGGT[C/T]ATAGCCTGTTCCTCT | 51455 |
| rs768725444 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491920 | AGTAGGCAGCCTCTG[C/T]AAAGGACGAAAAAAA | 51455 |
| rs768756603 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99421173 | ACTCAGACTTAACAC[A/G]CAACTCTAAACCCAT | 51455 |
| rs768756660 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99406712 | ACTTCAGAGTATCCA[A/G]TTCTCCCAAAATATA | 51455 |
| rs768765341 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99457038 | CCAAGCTAAACATTT[C/T]GATTCCTTTATGAAG | 51455 |
| rs768772858 | snp | G/T | 1.65021e-05 | 0.00287241 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404667 | AGTGCTTCTAAAACA[G/T]ACTGATCCAGCTATA | 51455 |
| rs768795656 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99469360 | TGTTTCCATGTGACT[C/G]TGTAAGACAGTCACA | 51455 |
| rs768799427 | snp | A/C | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483678 | ATCAAGACTTTAAAT[A/C]GTAATTTTACAAGAA | 51455 |
| rs768840735 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462565 | CATCCTTCTGCATAG[C/T]AGCATCTGATCGAAA | 51455 |
| rs768844587 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99408285 | TCTCCCTTCAAGGAA[A/G]CCAGAAATACCAAAT | 51455 |
| rs768852923 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401211 | ACTTATGGCACAGCT[A/C]TCAGAGAGCATCAGG | 51455 |
| rs768877273 | snp | C/T | 5.02424e-05 | 0.00501185 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410852 | GACTCAGAAGAAAAG[C/T]TTCTGCCTCTTTTGG | 51455 |
| rs768893105 | in-del | -/G | 6.63834e-05 | 0.00576084 | intron-variant | REV1 | GRCh38.p7 | 2:99421701 | CCACAGCCACCATCT[-/G]GGTAGACCCAATGTT | 51455 |
| rs768941770 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99429613 | TTTCTTTTGGTTCCT[A/C]CTACATGACCTATTG | 51455 |
| rs769005707 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99442741 | AACAGAGAATCATCA[A/G]GACTTCATCAAAATC | 51455 |
| rs769018954 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428081 | CCTGCTCCCCAGCCA[A/G]CATTCATCTTGGTGG | 51455 |
| rs769025905 | in-del | -/AC/G | 7.82434e-05 | 0.00625434 | intron-variant | REV1 | GRCh38.p7 | 2:99442266 | CAAAAAAAAAAAAAA[-/AC/G]AAAAAAAAAACCAAC | 51455 |
| rs769095560 | snp | A/G | 1.65883e-05 | 0.00287991 | intron-variant | REV1 | GRCh38.p7 | 2:99424128 | GAAAACACAGACACA[A/G]AATGACAGTTTGATA | 51455 |
| rs769224068 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461739 | CTGAAGCTGGCCATA[C/T]GGAAGCTTGGAAAGA | 51455 |
| rs769258226 | snp | C/T | 6.60055e-05 | 0.00574442 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435836 | CAAGAATACAGACCT[C/T]TGAGATCTGGTCTAT | 51455 |
| rs769279814 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464196 | TCTAGGGATTCAACT[A/G]TACTTTTCCTGAACT | 51455 |
| rs769280499 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403731 | GGTGAGTGCTGTTCT[C/T]GCCCTGCCTTTGTCT | 51455 |
| rs769289085 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482571 | AGCAGGTGCCCAAAT[C/T]ACACTACAGCTATAA | 51455 |
| rs769315424 | snp | A/C | 8.58038e-05 | 0.00654939 | intron-variant | REV1 | GRCh38.p7 | 2:99403152 | AAAATGATAGTATGG[A/C]TAGTCTGGATGACAG | 51455 |
| rs769321431 | snp | G/T | 1.68091e-05 | 0.00289901 | intron-variant | REV1 | GRCh38.p7 | 2:99434464 | CTGTGAGGAAAATAT[G/T]AAATTATTTCTGTAT | 51455 |
| rs769367884 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477818 | AAAAGATGCTTGATT[C/T]AACAAAATCAATAGT | 51455 |
| rs769371619 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463001 | GCTGAGGCAGGAGAA[C/T]TGCCTGAACCCAGGA | 51455 |
| rs769417262 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412865 | GACCAAATTCTTTTT[C/G]GAGTTTTGCCATGGT | 51455 |
| rs769429936 | snp | G/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434414 | TAAAGGTGCCCTTCC[G/T]GTGCCTCTGTTACTT | 51455 |
| rs769459854 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476512 | AGTGAGCCCAGATTG[C/T]GCCATTGCACTCCAG | 51455 |
| rs769465918 | snp | A/C | 0.0136381 | 0.0814437 | intron-variant | REV1 | GRCh38.p7 | 2:99442278 | AAAAAAAAAAAAAAC[A/C]AACCAGCTTTGCAGT | 51455 |
| rs769641015 | snp | A/G | 2.17176e-05 | 0.0032952 | intron-variant | REV1 | GRCh38.p7 | 2:99465000 | TCTGTATTGGGGAGG[A/G]AAAAAAAAATGTCAA | 51455 |
| rs769668424 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450526 | AATAATTAGGTGAGC[C/T]TTAGTTTCTAGAAGA | 51455 |
| rs769740037 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477069 | GATCTCATAAGTGAG[A/G]GTGGTCTTGGGACCC | 51455 |
| rs769765624 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99421375 | TGTCACACAATTGTA[A/G]GCAATGCTAAAAACG | 51455 |
| rs769795946 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456859 | TCCTCAGAGGCAAAA[G/T]AACAAACAGAAACAC | 51455 |
| rs769817518 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99444389 | CCTATGATCATTCTC[A/G]CTTTTCCTGCCCTAC | 51455 |
| rs769819988 | snp | C/T | 1.68264e-05 | 0.0029005 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410710 | CTGGCAATGTTATCA[C/T]AAATTCCATGGCCTC | 51455 |
| rs769820003 | snp | A/G | 3.54503e-05 | 0.00420998 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429944 | TGATGAATCTGGTAT[A/G]TCTGCTTTAAAAATA | 51455 |
| rs769840357 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99450030 | TTATAATTTTTATTT[G/T]TATTTAAGAAAATAT | 51455 |
| rs769869443 | snp | C/T | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405942 | CCTCTATACTCAGGT[C/T]AAGTCTCGACTGCAC | 51455 |
| rs769896597 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468652 | CAGTTTCTGAAACTG[A/T]GATTCACAACCTAAA | 51455 |
| rs769914687 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430250 | CACACAGTCCCTGGA[A/G]GTGGACATGGATGAG | 51455 |
| rs769967808 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477733 | TGATTAAAAGGAAAG[C/T]GTCTATCCCAAACAA | 51455 |
| rs770028430 | snp | A/T | 1.65652e-05 | 0.0028779 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438651 | TTCATTTTTTTTAAC[A/T]TTTCCCTTCCTGGAA | 51455 |
| rs770076069 | snp | A/T | 6.61233e-05 | 0.00574955 | intron-variant | REV1 | GRCh38.p7 | 2:99401372 | AGGTGGGGAGAGAAG[A/T]AATGTCATTAGGAAT | 51455 |
| rs770091141 | snp | C/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490763 | CTGAGTATTTGTAAA[C/G]GGAGGGCCGGTATCC | 51455 |
| rs770111927 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99486532 | GACTCCATCTCAAAA[-/A]AAAAAAAAAATTACC | 51455 |
| rs770127623 | snp | A/G | 1.66178e-05 | 0.00288247 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401226 | ATCAGAGAGCATCAG[A/G]CTCTCTGGTAATATT | 51455 |
| rs770132219 | snp | A/G | 0.000132172 | 0.00812827 | intron-variant | REV1 | GRCh38.p7 | 2:99402840 | TTGCTATATTCACAC[A/G]TTATCCAGGTATATT | 51455 |
| rs770138580 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99429775 | AAGATTATAGTTCAA[G/T]AAATTATATAAAAAT | 51455 |
| rs770170559 | snp | A/C | 3.41472e-05 | 0.00413188 | intron-variant | REV1 | GRCh38.p7 | 2:99418982 | TCCAAGAAATAGTCA[A/C]AATTATTTTTTAAAT | 51455 |
| rs770177404 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461621 | AAATACAATGAAATG[A/G]TAAGAAGAAGAATCC | 51455 |
| rs770188297 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99403438 | TGAACAAGTATTTAA[G/T]ACATTTGTGGTAATG | 51455 |
| rs770204183 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452806 | ATAAATACTTAAAAT[C/T]TCAAAACACTTATTC | 51455 |
| rs770228092 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415704 | GGCTACGTAGCTACT[A/G]TATTAGTGCAGACTT | 51455 |
| rs770232360 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430982 | ACAAATCTATTTTGA[A/G]TGCACTGTAACAACA | 51455 |
| rs770255467 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433122 | ACTTCCTTAAGCTAT[-/TTC]TTATTTTCTAGAACT | 51455 |
| rs770255934 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401075 | ACAATTATTTACATG[A/C]AATACTGACAAATTT | 51455 |
| rs770269067 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460365 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCTGAAAA | 51455 |
| rs770317922 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404559 | AAAATTCCTGTATTA[A/C]AGCCATTTACTGGTT | 51455 |
| rs770322086 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99416490 | ATTTTATGAAAACCA[A/C]ATGAACCACTGTGAG | 51455 |
| rs770352544 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487438 | CACTATGGAAACACT[C/T]CAACCAAGAGATAAT | 51455 |
| rs770363119 | snp | G/T | 1.70551e-05 | 0.00292015 | intron-variant | REV1 | GRCh38.p7 | 2:99449332 | TTTAATAAATTAAAC[G/T]TACCTTTCCACAATC | 51455 |
| rs770364551 | snp | C/G | 1.95494e-05 | 0.00312639 | intron-variant | REV1 | GRCh38.p7 | 2:99438529 | TATTGACCAGAAATA[C/G]CAATAATAGCATAAG | 51455 |
| rs770375648 | in-del | -/C | 0.000675425 | 0.0183645 | intron-variant | REV1 | GRCh38.p7 | 2:99403678 | CATTTTTGTTACATG[-/C]CACTTCCAAGGCTCA | 51455 |
| rs770401117 | snp | A/C | 1.6671e-05 | 0.00288708 | intron-variant | REV1 | GRCh38.p7 | 2:99442268 | AAAAAAAAAAAAAAA[A/C]AAAAAAAACCAACCA | 51455 |
| rs770404522 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438725 | CAATTCACACTTCCA[A/C]ATTGATATGTGATGC | 51455 |
| rs770445058 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472576 | AAGTAGTTCTGAAGC[C/T]GGAAACACTGTATAG | 51455 |
| rs770454967 | snp | A/C | 2.54249e-05 | 0.00356536 | intron-variant | REV1 | GRCh38.p7 | 2:99449556 | TGTGTAAGAAGTAGA[A/C]CCCTAATGAATAACT | 51455 |
| rs770461977 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415385 | ACTTGGCATCTGTCC[C/T]TGAAGGGGAACTATT | 51455 |
| rs770480152 | snp | G/T | 5.08738e-05 | 0.00504324 | intron-variant | REV1 | GRCh38.p7 | 2:99403129 | CAGATGGATATAAGA[G/T]CCTCAACAAAATGAT | 51455 |
| rs770498794 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475361 | TGAGAAGGATAAAAA[C/T]ACTTTTAAATAAGGA | 51455 |
| rs770586492 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406367 | TCTTAGCTTTCTGAA[C/T]TTGGAAGACATCACG | 51455 |
| rs770671693 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99478088 | AATACAAAAATTAGC[C/T]GAGCGTGGTGGTGCA | 51455 |
| rs770683662 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440937 | GCCTAGACAAATGGA[C/G]ATTTGCAAAGTAGCT | 51455 |
| rs770705185 | snp | A/T | 3.29658e-05 | 0.00405978 | intron-variant | REV1 | GRCh38.p7 | 2:99462627 | ATATACCCACCCTAG[A/T]ATTAAAGAAAAGGTA | 51455 |
| rs770710822 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99436273 | ATCTACAAACGCGCC[C/T]GGATAAAATAACAAC | 51455 |
| rs770741776 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99415077 | ACCGGAGGTGGGGGA[A/G]GGAGGCAGGGCATGT | 51455 |
| rs770796596 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99421441 | ACTCCATAAAATTAA[A/C]TGATATTCAAGAATC | 51455 |
| rs770800580 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99437252 | CCTCCGAAAGTGTGC[A/G]AATTACAGGCATGAG | 51455 |
| rs770802820 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412828 | CCACGGCAGAACCTA[C/T]AAAGCATCTGACCTG | 51455 |
| rs770804025 | snp | C/T | 1.65751e-05 | 0.00287876 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405933 | GTGACGGGACCTCTA[C/T]ACTCAGGTTAAGTCT | 51455 |
| rs770873135 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99445957 | GAGTATGTAACGTTT[A/C]TTAAATAGCTAATAC | 51455 |
| rs770879863 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99425329 | ATGTTTATAAAAATA[-/TT]GTAATATTATAAATG | 51455 |
| rs770884038 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409665 | CCTTGCCAACATAGT[A/G]AAACCCTATCTCTAC | 51455 |
| rs770893499 | snp | A/G | 1.66388e-05 | 0.00288429 | intron-variant | REV1 | GRCh38.p7 | 2:99424290 | AGTTGCCTAGAGCGA[A/G]AACAAAACACAATGG | 51455 |
| rs770937537 | in-del | -/AAAAAAC | 0.000700253 | 0.0186986 | intron-variant | REV1 | GRCh38.p7 | 2:99442270 | AAAAAAAAAAAAAAA[-/AAAAAAC]AAAAAACCAACCAGC | 51455 |
| rs770964496 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99450763 | ACATGTAATCAACAG[-/A]AAAAAATCTGAGATA | 51455 |
| rs770983642 | in-del | -/AAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99416914 | CAAGACTCCATCTCA[-/AAAAAA]AAAAAAAAAAAAAAG | 51455 |
| rs770985442 | snp | C/T | 1.65302e-05 | 0.00287486 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408070 | TCATTGTATGAAACA[C/T]GTTTAGCATCGCCTT | 51455 |
| rs770986238 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99479328 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 51455 |
| rs770993014 | snp | A/T | 4.9629e-05 | 0.00498117 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434431 | TGCCTCTGTTACTTG[A/T]AACAGCCACTGGTTT | 51455 |
| rs770998843 | snp | C/G/T | 8.24415e-05 | 0.00641987 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412753 | AACCTTATTCCATAG[C/G/T]TGATCTCAGCTGAAA | 51455 |
| rs771049133 | snp | C/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406004 | CCTGAAGACTCAGCC[C/T]TGTTAGTATCAGGAC | 51455 |
| rs771065374 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466091 | GGACTACAGGTGCCC[-/G]CCACCACGCCCGATT | 51455 |
| rs771081402 | snp | G/T | 1.64887e-05 | 0.00287125 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438825 | GCCTTGCTAAACGTA[G/T]ATACTGAAGAAGTGC | 51455 |
| rs771090017 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459637 | CTTGAACCTGGGATG[C/T]TGAAGCTGCAGTGAG | 51455 |
| rs771108591 | snp | A/G | 7.17039e-05 | 0.00598722 | intron-variant | REV1 | GRCh38.p7 | 2:99429815 | AATTATTCATTAAGA[A/G]TTGTAACACACAACT | 51455 |
| rs771162296 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99407346 | ACCTGAGGTCAGGAG[A/T]TTGAAACCAGCCTGG | 51455 |
| rs771165682 | snp | C/T | 2.12601e-05 | 0.00326031 | intron-variant | REV1 | GRCh38.p7 | 2:99449322 | ATTAATTAAATTTAA[C/T]AAATTAAACTTACCT | 51455 |
| rs771172085 | snp | A/G | 1.69576e-05 | 0.00291179 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402379 | CTTCAAATGAGGACC[A/G]GTCTTTTTGAAGGAG | 51455 |
| rs771172912 | snp | A/G | 3.3018e-05 | 0.00406299 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438909 | GTGTTACTGTGCAAA[A/G]GTGATAATGAGAAAG | 51455 |
| rs771180203 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432209 | ATACCCTGGTTGCAC[A/G]GGGCTAATTAAAGAG | 51455 |
| rs771199817 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447298 | CTGCCTCAGCCTCCC[A/G]GGTAGCTGGGACTAC | 51455 |
| rs771212070 | in-del | -/AAA/AAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99473365 | GAGCGAGACTGTCTC[-/AAA/AAAA]AAAAAAAAAAAAAAG | 51455 |
| rs771243962 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411581 | TGGCTAATTTTTTTG[-/T]TATTTTTAGTAGAGA | 51455 |
| rs771257262 | snp | A/C | 1.66454e-05 | 0.00288486 | intron-variant | REV1 | GRCh38.p7 | 2:99435977 | TTCAAACCCCAAGCT[A/C]ATTTTTACTATTTAA | 51455 |
| rs771265918 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418059 | CATTTCTGTCGTTTA[A/T]TATTTATGGCCTGTT | 51455 |
| rs771272876 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416576 | AAATCTCCCTTAGGA[A/G]ATTCAAGGCTGTGCC | 51455 |
| rs771290918 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454366 | ACCAAGTCTGACCAA[C/T]ATGGAGAAACCCCGT | 51455 |
| rs771300346 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462715 | AACTAAATAAATAAA[C/T]GGACCTTATTCTGTG | 51455 |
| rs771340591 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439769 | CATGGTCAATAAATA[C/T]CTGCTGAATTAATAT | 51455 |
| rs771345892 | in-del | -/TA | | | intron-variant | REV1 | GRCh38.p7 | 2:99420317 | AATTCCTAAAGACAG[-/TA]TAAACCTCTTACCTG | 51455 |
| rs771352858 | in-del | -/GC | 3.02851e-05 | 0.00389123 | intron-variant | REV1 | GRCh38.p7 | 2:99403113 | TCTTTGGCACTAAGA[-/GC]AGATGGATATAAGAT | 51455 |
| rs771383124 | snp | A/G | 1.65146e-05 | 0.0028735 | intron-variant | REV1 | GRCh38.p7 | 2:99404400 | TTGGAGCAGGGGGGT[A/G]AGAATATTGAAACTA | 51455 |
| rs771449260 | in-del | -/A | 3.34202e-05 | 0.00408766 | intron-variant | REV1 | GRCh38.p7 | 2:99412963 | ACTCCTAGGAAAGGG[-/A]ATATAGTTAAGTATG | 51455 |
| rs771457519 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99473755 | AACACAGAATTCAAA[A/G]AACTTCAATCTATCA | 51455 |
| rs771544194 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416366 | AACCCCTTTTTAAAG[A/G]AACAGCTTATAATCT | 51455 |
| rs771547730 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487760 | TGCTCTTTAGTGTAG[C/G]ACTTGTTCATTTATT | 51455 |
| rs771549807 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421759 | TTTCTATTTCCTCAC[A/T]AAGCATTTTAAATGA | 51455 |
| rs771551406 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460801 | TATCCTGCAGAAAAG[A/G]ATAGAGATAATAACA | 51455 |
| rs771570818 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99452322 | GTCCCAGCTACTAGG[G/T]AGTCTGAAGTGGATA | 51455 |
| rs771579273 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403762 | TTGATCATACGCTGC[C/T]TTCAGCTCCCTCTGA | 51455 |
| rs771612603 | snp | C/T | 1.64974e-05 | 0.00287201 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406359 | GGTGGATTTCTTAGC[C/T]TTCTGAACTTGGAAG | 51455 |
| rs771619385 | snp | C/T | 3.30175e-05 | 0.00406296 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439069 | AAAGCCTGCTGGCAA[C/T]ACTGTTGACCATGGG | 51455 |
| rs771636020 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99403257 | GGCAGTGAATGGCAA[C/T]GGCCCAAAGTACAGG | 51455 |
| rs771654498 | snp | C/T | 3.30387e-05 | 0.00406427 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402896 | GGAATTACCAGGGGT[C/T]TCTCTGCAGGAGGTC | 51455 |
| rs771655639 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99438300 | GATAGATGTTATATT[A/C]ACACAGTTCAAAACT | 51455 |
| rs771662748 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99437401 | TGCCCATAGTCCTGC[A/G]GCCTAAGAGTGGCAG | 51455 |
| rs771715757 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99405372 | TAGTTTTGCAGCCAG[-/T]TATTTAACATCTCCT | 51455 |
| rs771716845 | snp | A/C | 1.66316e-05 | 0.00288367 | intron-variant | REV1 | GRCh38.p7 | 2:99418971 | AAAAAAAGTCATCCA[A/C]GAAATAGTCACAATT | 51455 |
| rs771767406 | snp | C/G | 1.65138e-05 | 0.00287343 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439122 | AAGGCACCATTAGAG[C/G]TAGGAGTGTGTCCAT | 51455 |
| rs771768236 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99457608 | AGAATCGCTTGAGCC[-/A]AGGGAGGCAGAGGGT | 51455 |
| rs771849269 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99423102 | TTATCATTCAGCACT[C/T]ACTCCTACATAATGA | 51455 |
| rs771867465 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99463163 | TCCCTCTATCAACTC[-/AA]GTTTTAATTTTATTA | 51455 |
| rs771881505 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99466240 | ACAGGCGTAAGCCAC[C/T]GTGCCCGGCCTCTTT | 51455 |
| rs771891171 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403010 | TTGTTATTCAAAGGA[C/G]TCTGAATCCTTTTTG | 51455 |
| rs771912910 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99446771 | GTGGGGGGATTACAT[A/G]CATGAGCTATCGCAC | 51455 |
| rs771939023 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99424486 | GTGTAAATGACACAT[A/G]TAGATGTGCCAACTA | 51455 |
| rs771939229 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99409949 | TACCAATTAAATGTA[C/T]ACACCTATGTAAATG | 51455 |
| rs771945223 | snp | G/T | 1.7011e-05 | 0.00291637 | intron-variant | REV1 | GRCh38.p7 | 2:99434310 | CAGGAGCACTAAGAC[G/T]TCAAAGAGAGCTCAT | 51455 |
| rs771969836 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99479626 | AGACCTCATCTCTAC[-/A]AAAAAAAATAAAAAT | 51455 |
| rs772000952 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447577 | AACAGTAGCTTCTTA[C/T]ATATTACACCTCTAC | 51455 |
| rs772023742 | snp | A/G | 0.0001154 | 0.00759518 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438822 | GCTGCCTTGCTAAAC[A/G]TAGATACTGAAGAAG | 51455 |
| rs772026845 | snp | A/G | 1.7357e-05 | 0.00294588 | intron-variant | REV1 | GRCh38.p7 | 2:99410687 | TATCATTTCTGAGGT[A/G]AGCTTACCTGGCAAT | 51455 |
| rs772061826 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99479077 | GCTCATACCTGTAAT[C/T]CCAGCACTTTAGGAG | 51455 |
| rs772087286 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418299 | TGAGAAAGGTTAAGA[G/T]GGAAGGTTTTTTTCC | 51455 |
| rs772101351 | snp | C/T | 1.67849e-05 | 0.00289692 | intron-variant | REV1 | GRCh38.p7 | 2:99401398 | GGAATTAGGAAAGGT[C/T]CTTAAGACTAATTAT | 51455 |
| rs772101562 | in-del | -/TG | | | intron-variant | REV1 | GRCh38.p7 | 2:99465391 | GTGGCTTTTAAACTC[-/TG]TCTTTGCTATTACAT | 51455 |
| rs772141695 | snp | C/G | 1.65548e-05 | 0.002877 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439265 | ACTGTTCATGCCATT[C/G]ACTTTGACTTCATTT | 51455 |
| rs772153977 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99478057 | GGCCAAAATGGCAAA[A/C]TCCCATCTTTATAAA | 51455 |
| rs772175158 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99405108 | CTTTCAGATGAGAGA[C/T]TGCCCAAAAATACAA | 51455 |
| rs772194824 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99477629 | TTAAAAATAGACAAA[A/C]AATAAGATGTACTGT | 51455 |
| rs772214707 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99401423 | AATTATTCCTTTTTA[G/T]ATATAAAAATTGACT | 51455 |
| rs772218362 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462607 | ATTTCTGGACCTTGG[C/T]AGCCATATACCCACC | 51455 |
| rs772219558 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99458770 | AAGCCAGCCCCAAAA[C/G]GTTATATGCTGTATG | 51455 |
| rs772222209 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403642 | TAATTAGACAACAGT[A/G]ACTCCATTACTCTTT | 51455 |
| rs772279840 | snp | A/T | 1.65255e-05 | 0.00287445 | intron-variant | REV1 | GRCh38.p7 | 2:99462460 | AATCCTAATAAAAAT[A/T]CATGCCAAAATAGGG | 51455 |
| rs772295601 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483914 | CTCTGGAGTCTGTAA[C/G]ATTCTTCCTACCCCT | 51455 |
| rs772305731 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470683 | CTCCTCTGCCTTTGC[C/T]TCTTTTAAAACAAGA | 51455 |
| rs772312599 | in-del | -/CTCTATCTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99430082 | TATCTCTATTGGTAT[-/CTCTATCTC]TATCTCCTTATCTAA | 51455 |
| rs772346039 | snp | C/T | 1.65356e-05 | 0.00287533 | intron-variant | REV1 | GRCh38.p7 | 2:99424144 | AATGACAGTTTGATA[C/T]ACTGTACCTTGCCAA | 51455 |
| rs772395148 | snp | A/C | 0.000261572 | 0.0114332 | intron-variant | REV1 | GRCh38.p7 | 2:99442282 | AAAAAAAAAACCAAC[A/C]AGCTTTGCAGTAATC | 51455 |
| rs772418770 | snp | A/G | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406345 | TTGTGCTCCTCTTCG[A/G]TGGATTTCTTAGCTT | 51455 |
| rs772434917 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455864 | GTTTCATTTTGTGAA[C/T]TGTGCTAAAGTACTT | 51455 |
| rs772450662 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427802 | AGTTAAATTCATTTT[C/T]ATCACTTTATGTATC | 51455 |
| rs772484137 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442384 | CAGGTCTGCATACAG[G/T]ATTAAAGCTGAGACC | 51455 |
| rs772488229 | snp | C/T | 1.6898e-05 | 0.00290667 | intron-variant | REV1 | GRCh38.p7 | 2:99434477 | ATTAAATTATTTCTG[C/T]ATGTGGTACAGGAAT | 51455 |
| rs772510549 | in-del | -/TTAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99447150 | TTAATATGTAAAATG[-/TTAT]TTATTTGACTTTTTT | 51455 |
| rs772532776 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99426448 | ACACAAAAATTTTCC[A/G]AAGCACATTACTTAG | 51455 |
| rs772542060 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475261 | CACATTCTGTATTTG[C/T]TCCGATTGGCTAGCA | 51455 |
| rs772580288 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99472445 | AAGAGTTCTGGAGAT[-/G]GGATAGTGGTGATGG | 51455 |
| rs772587006 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462488 | GGGTTAAGTAAAAAG[C/T]ACTCAACCTGTGTAT | 51455 |
| rs772647318 | snp | C/T | 4.98832e-05 | 0.00499391 | intron-variant | REV1 | GRCh38.p7 | 2:99424287 | CCAAGTTGCCTAGAG[C/T]GAGAACAAAACACAA | 51455 |
| rs772648976 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99419885 | CTTGGTTTTATAGAA[G/T]ACTTATATAAACAGA | 51455 |
| rs772697184 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99435486 | GCTCAAGAGAAAGCA[C/T]AGTGACCCAAGTCTC | 51455 |
| rs772706921 | snp | C/T | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406362 | GGATTTCTTAGCTTT[C/T]TGAACTTGGAAGACA | 51455 |
| rs772718270 | snp | A/G | 1.65086e-05 | 0.00287298 | intron-variant | REV1 | GRCh38.p7 | 2:99406507 | TAGAACCCAGAATAA[A/G]GAGTATGCTTCTAGG | 51455 |
| rs772744691 | snp | C/T | | | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408037 | TACTTACCCCTCTCA[C/T]ATCTGATATATTTAG | 51455 |
| rs772747051 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417827 | AATATACCAGTTCCT[C/T]CTTATATAAAACTTC | 51455 |
| rs772811158 | snp | A/G | 1.66543e-05 | 0.00288563 | intron-variant | REV1 | GRCh38.p7 | 2:99418975 | AAAGTCATCCAAGAA[A/G]TAGTCACAATTATTT | 51455 |
| rs772813252 | snp | A/T | 1.6722e-05 | 0.00289149 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406074 | AAGTTCTAGAAGCAG[A/T]TGATATTTCCAGATC | 51455 |
| rs772815959 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99486131 | CCCTGTCTCAAAAAA[C/T]GTTAAAAAAGAAAAA | 51455 |
| rs772836045 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487769 | GTGTAGGACTTGTTC[A/G]TTTATTTGGAGACGA | 51455 |
| rs772849097 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447822 | ATCTCCTGGGTTCAC[A/G]CGATTCTCCTGCCTC | 51455 |
| rs772863714 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439123 | AGGCACCATTAGAGC[C/T]AGGAGTGTGTCCATT | 51455 |
| rs772870983 | snp | A/T | 3.29832e-05 | 0.00406085 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412746 | CTGAGTAAACCTTAT[A/T]CCATAGTTGATCTCA | 51455 |
| rs772902750 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | REV1 | GRCh38.p7 | 2:99406157 | ATCATCGGGCAGGGC[C/T]TTTAATCCTCTGTCC | 51455 |
| rs772937394 | in-del | -/A | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440458 | AGCCTGACTACACAG[-/A]AAAGTCCCACAAGCT | 51455 |
| rs772947679 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99448901 | AAATCCTAGGCTATA[A/G]TATTATCAACATGAG | 51455 |
| rs772954741 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421389 | AAGCAATGCTAAAAA[C/T]GGTTTTACAAGTGAG | 51455 |
| rs773037542 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99434541 | ATTTTAAAAACATGC[C/T]TTTTTTTTCTTTAGC | 51455 |
| rs773044441 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99408397 | TCAACTAAAAATAAG[C/T]TGAGAAATTTAGAAA | 51455 |
| rs773045081 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99420428 | CCCCTATAGCCCAGA[A/G]CCCACCAGAATTACT | 51455 |
| rs773058644 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99453742 | TACTAAAAATACAAA[A/C]ATCAGCTGGGCATGG | 51455 |
| rs773067128 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99443027 | CACCAGTGTTCTAAC[A/G]CTAGGTGGTACTAGC | 51455 |
| rs773086839 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477859 | TGAAGGGGGCTTCCT[A/G]AAACAACGACTAATG | 51455 |
| rs773108162 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99410252 | CTGGCCTCAAGTGAT[C/G]CAGCTGCCTCAGCCT | 51455 |
| rs773144890 | snp | G/T | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403020 | AAGGACTCTGAATCC[G/T]TTTTGGTGAACCAAT | 51455 |
| rs773185065 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99466297 | ACCCAGGCTGAAGTG[C/T]AGTGGCACGATCTCG | 51455 |
| rs773221368 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468387 | CAGGATACCACTACT[C/T]GACAGAAATATCCTT | 51455 |
| rs773244384 | snp | G/T | 2.3622e-05 | 0.00343663 | intron-variant | REV1 | GRCh38.p7 | 2:99429969 | AAAATAAAAAAAAAT[G/T]AATGGTTATATGTTA | 51455 |
| rs773258544 | in-del | -/TG | 0.000129458 | 0.0080444 | intron-variant | REV1 | GRCh38.p7 | 2:99424927 | GGTAAATTTTAAATC[-/TG]TGTGTCTCAGTGCCC | 51455 |
| rs773260337 | snp | A/C | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438740 | CATTGATATGTGATG[A/C]AGTCTTGAATGAGAA | 51455 |
| rs773271510 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99479140 | CGAGACCACACTGGC[C/T]AACATGGTGAAATCC | 51455 |
| rs773322311 | snp | A/G | 1.69686e-05 | 0.00291273 | intron-variant | REV1 | GRCh38.p7 | 2:99434314 | AGCACTAAGACTTCA[A/G]AGAGAGCTCATTTGT | 51455 |
| rs773329564 | snp | C/T | 1.64982e-05 | 0.00287208 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424160 | ACTGTACCTTGCCAA[C/T]GTTTCATACAATGTT | 51455 |
| rs773332014 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459485 | CTGAGGCAGAAGAAT[C/T]GCTTGAGCCTAGGAG | 51455 |
| rs773365275 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478089 | ATACAAAAATTAGCC[A/G]AGCGTGGTGGTGCAC | 51455 |
| rs773377315 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462613 | GGACCTTGGCAGCCA[C/T]ATACCCACCCTAGAA | 51455 |
| rs773421963 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458795 | TGTATGTTTTATTTA[C/T]ATAACATTCTTGAAA | 51455 |
| rs773448550 | snp | C/T | 9.132e-05 | 0.0067566 | intron-variant | REV1 | GRCh38.p7 | 2:99402196 | GTACACCCTCAGCCA[C/T]TGTGACATGCCATTT | 51455 |
| rs773504209 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99430050 | ATATAAAAATGTTCA[A/G]TAAATTCCAAATACA | 51455 |
| rs773515762 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444789 | TTATCTGAAAGCATA[G/T]TTGTATAAGACCTTT | 51455 |
| rs773550136 | in-del | -/CT | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482662 | AGTTAGGTAAAAGCA[-/CT]CTTTAAGATATAAAA | 51455 |
| rs773572702 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470729 | GCCAATCAGAACAAA[C/T]ACAGAATGTGAGGTC | 51455 |
| rs773583595 | snp | A/G | 1.69602e-05 | 0.00291201 | intron-variant | REV1 | GRCh38.p7 | 2:99434483 | TTATTTCTGTATGTG[A/G]TACAGGAATGTTAAC | 51455 |
| rs773609564 | in-del | -/CA | | | intron-variant | REV1 | GRCh38.p7 | 2:99426818 | TTCCTACATTTAAAG[-/CA]CAGAGGACATATTCT | 51455 |
| rs773658504 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483940 | CCCCTGACATTCTGA[A/G]GTGTTGAGAAGCCAA | 51455 |
| rs773672570 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99487651 | AGTAAAAAAAAACTT[C/T]TCATTTTTAAATGTT | 51455 |
| rs773688193 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416517 | TGAGCAATACAGAAC[C/G]TGGCTCTGAAGAAGA | 51455 |
| rs773697582 | in-del | -/AG | | | intron-variant | REV1 | GRCh38.p7 | 2:99449926 | CCTCCAGAGTATACA[-/AG]AGGAGTCAGATAAAT | 51455 |
| rs773727639 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406037 | GTCGGCAGATGTGCA[A/G]GAAAAGGTGGCAAGA | 51455 |
| rs773742845 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439534 | TTGCAAAAGTAGCAA[A/G]ATAACTAGAAAAATT | 51455 |
| rs773764735 | in-del | -/CACTT | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99400980 | TTAAACAACTGTAAA[-/CACTT]CACTTCACTGTAAAA | 51455 |
| rs773772861 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99420035 | CTTGAACTTAAAAGA[A/C]TGGATTCACATGATC | 51455 |
| rs773788414 | snp | C/T | 6.21987e-05 | 0.00557633 | intron-variant | REV1 | GRCh38.p7 | 2:99406513 | CCAGAATAAAGAGTA[C/T]GCTTCTAGGAAAACT | 51455 |
| rs773793667 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99487028 | TTTAGAATTAGAAAA[A/G]GCCTGAGGCGATGAC | 51455 |
| rs773794208 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99459323 | CATATTACCATTTGG[C/G]GAAACTGGGTAAAGG | 51455 |
| rs773814749 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400711 | AGATTTCTCCGCATG[C/G]AAGAAGTAGTAAAGA | 51455 |
| rs773918509 | in-del | -/A | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483673 | TAAAATCAAGACTTT[-/A]AAATCGTAATTTTAC | 51455 |
| rs773939517 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99472587 | AAGCTGGAAACACTG[C/T]ATAGGCACCTGCAAG | 51455 |
| rs773940606 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486007 | GCACATGCCTGTAGT[A/G]CAGGCTACTCGAGCG | 51455 |
| rs773951235 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412890 | CATGGTCATATACTG[C/T]AAGTCTCCACAAGTT | 51455 |
| rs773964797 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464499 | ATATAATCATACAAA[A/G]TATTTCTTTGTAACA | 51455 |
| rs774005480 | snp | A/C | 8.57229e-05 | 0.0065463 | intron-variant | REV1 | GRCh38.p7 | 2:99429963 | GCTTTAAAAATAAAA[A/C]AAAATTAATGGTTAT | 51455 |
| rs774040910 | snp | A/G | 1.66638e-05 | 0.00288645 | intron-variant | REV1 | GRCh38.p7 | 2:99418800 | GTAATGCCTGTAATA[A/G]AAGTATTGTTAAAAT | 51455 |
| rs774077257 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99409703 | ACAAAAATTCGCTGG[A/G]CATGGTGGCATGCCC | 51455 |
| rs774088612 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99436302 | ACAATAAAAGTGACT[A/G]CTATTATCCAGTGCT | 51455 |
| rs774097504 | snp | C/G | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402767 | GCAAACTAGAAAGGC[C/G]TGGCACACCTGAAGT | 51455 |
| rs774116457 | snp | C/T | 1.651e-05 | 0.0028731 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410741 | CAAATTTTGCAGTTT[C/T]TACAGGAGCCCCAGG | 51455 |
| rs774171195 | in-del | -/CT | | | intron-variant | REV1 | GRCh38.p7 | 2:99409834 | GGTGACAGAGCCAGA[-/CT]CTGTCTCAAAACAAA | 51455 |
| rs774176289 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437324 | CCCATGAGGCAAACA[C/T]CATGGACTATCTATC | 51455 |
| rs774179251 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99475011 | TATTTTAGTTCCTCC[A/G]TATGTGGAAAGAGTT | 51455 |
| rs774193712 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99416911 | AGCAAGACTCCATCT[-/AA]CAAAAAAAAAAAAAA | 51455 |
| rs774214194 | in-del | -/AAAAAC | 2.32561e-05 | 0.00340991 | intron-variant | REV1 | GRCh38.p7 | 2:99442271 | AAAAAAAAAAAAAAA[-/AAAAAC]AAAAACCAACCAGCT | 51455 |
| rs774222253 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99444647 | AATTAAAGCCCAATG[C/G]ACTACAGTAATGTTA | 51455 |
| rs774222333 | in-del | -/GAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99420720 | AGACAGGGAACTTTG[-/GAA]GAAGAAGGGTTTTTG | 51455 |
| rs774241488 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99463401 | GTGCATGCCTGTAAT[C/T]CCAGTTACTCAGGAG | 51455 |
| rs774254139 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99434555 | CCTTTTTTTTCTTTA[C/G]CTTTACTTAGACATT | 51455 |
| rs774262850 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99423083 | AATAGCTATAATAAG[C/T]GTCTTATCATTCAGC | 51455 |
| rs774286577 | snp | C/T | 0.000258565 | 0.0113673 | intron-variant | REV1 | GRCh38.p7 | 2:99406151 | CTTCAGATCATCGGG[C/T]AGGGCCTTTAATCCT | 51455 |
| rs774310840 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99446315 | TATATAATCATGCTG[C/T]CCAAAATCACTCTTA | 51455 |
| rs774315498 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99465000 | TCTGTATTGGGGAGG[-/AA]AAAAAAAATGTCAAT | 51455 |
| rs774331574 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99476767 | CAGTACAAATGCTGG[A/G]CACCAAGGCTTGGGT | 51455 |
| rs774374773 | snp | A/T | 1.65302e-05 | 0.00287486 | intron-variant | REV1 | GRCh38.p7 | 2:99402865 | TATATTAAGATCTCA[A/T]AAAGGTCAAAGTTAA | 51455 |
| rs774379931 | snp | A/G | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401248 | GGTAATATTTATGTA[A/G]CTTTTAATGTGCTTC | 51455 |
| rs774388913 | snp | A/T | 1.67396e-05 | 0.00289301 | splice-donor-variant | REV1 | GRCh38.p7 | 2:99429838 | ACACAACTTCTACAT[A/T]CCTGGCCTCATAACT | 51455 |
| rs774412439 | snp | C/T | 6.60229e-05 | 0.00574518 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99449375 | ATTACTTTTTCCCCC[C/T]TTAATTCTTTAATTT | 51455 |
| rs774435284 | in-del | -/AACTT | | | intron-variant | REV1 | GRCh38.p7 | 2:99464842 | TACAATTTAGAAAAC[-/AACTT]AAACCACATTATAAC | 51455 |
| rs774445926 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458486 | ACAAGGCTAGTGGGA[G/T]TATAAAATACTACAA | 51455 |
| rs774455544 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418110 | TTCGGACATACTTTT[A/T]TTAGGCTTAAAAATA | 51455 |
| rs774469433 | snp | G/T | 1.65759e-05 | 0.00287883 | intron-variant | REV1 | GRCh38.p7 | 2:99401384 | AAGAAATGTCATTAG[G/T]AATTAGGAAAGGTCC | 51455 |
| rs774470983 | snp | A/G | 3.30289e-05 | 0.00406366 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439110 | TCCTGTGTCTTTAAG[A/G]CACCATTAGAGCTAG | 51455 |
| rs774501808 | snp | A/G | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491982 | AAAGAGAGATGGGGA[A/G]TACATAAATAAAAAT | 51455 |
| rs774541693 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99456344 | CACTTGTATTCCACT[A/G]AGGAGACAAAAATAA | 51455 |
| rs774547394 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469619 | GACTTCCTCTTTCCA[C/T]TCTCTCAATAGGGAT | 51455 |
| rs774554205 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99470626 | TTGAAGGTGTTTTTA[-/C]CTTTCTCTACATTCC | 51455 |
| rs774562166 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99416581 | TCCCTTAGGAAATTC[A/C]AGGCTGTGCCTCAGC | 51455 |
| rs774570960 | snp | C/T | 3.4256e-05 | 0.00413845 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403044 | AACCAATGGTTTTTT[C/T]CTTCTTGTTTCTTTT | 51455 |
| rs774572804 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439837 | TTACTTGAATTCTTA[G/T]TCCTAGTTTTAGTTT | 51455 |
| rs774589573 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438704 | TAGGGTATTGACAAA[C/T]TCAGTCAATTCACAC | 51455 |
| rs774639364 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99481969 | ATGAATCCATAATGG[A/G]TCCTCCTTGGCCCAC | 51455 |
| rs774655222 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99426329 | CTCAGCCTGGGCAAC[-/AA]GAGCGAAATTCTATC | 51455 |
| rs774656165 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99465682 | ACCCCTTGTAAAGTC[-/AA]AGCCTTTTAACACAA | 51455 |
| rs774700413 | snp | C/T | 1.84211e-05 | 0.00303483 | splice-acceptor-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439311 | TTAACGATGTGATTT[C/T]TAAAGCAGGAAAAAA | 51455 |
| rs774703040 | snp | A/C | 0.000139053 | 0.0083371 | intron-variant | REV1 | GRCh38.p7 | 2:99451535 | CACATAAACTATGGA[A/C]TAAGACCGATCTGAG | 51455 |
| rs774720086 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99461752 | TATGGAAGCTTGGAA[A/G]GAAGCTGCTTGTTAC | 51455 |
| rs774729180 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480774 | TAAATGTAATTCCAA[A/G]TAAACATAAAGGAAG | 51455 |
| rs774732084 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99419205 | AGAAAGCAGTCCTGA[-/TT]TTTTTTTTTTTTTTT | 51455 |
| rs774734587 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99403833 | AGTGGAAAAGACGAG[A/G]TCAAAGTCAAACCTG | 51455 |
| rs774765084 | snp | C/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406395 | ACGGACAGAGTATGA[C/G]CCACTAGGAAAGTGG | 51455 |
| rs774770479 | snp | C/T | 4.32779e-05 | 0.00465157 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406485 | CTGATTCACGTGAAT[C/T]CCAACCTAGAACCCA | 51455 |
| rs774770599 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99455724 | AATTAGACTTGTCAA[A/C]ACTAAAGAGAATCCT | 51455 |
| rs774783992 | snp | A/G | 9.22382e-05 | 0.00679048 | intron-variant | REV1 | GRCh38.p7 | 2:99438559 | GAGCAAAATGATCAA[A/G]CATGACTGTTTCTTA | 51455 |
| rs774844880 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412869 | AAATTCTTTTTGGAG[C/T]TTTGCCATGGTCATA | 51455 |
| rs774862964 | in-del | -/GGA | | | intron-variant | REV1 | GRCh38.p7 | 2:99415348 | GTCAAGGAGGCTCCT[-/GGA]GGTCAAGCAACTGGG | 51455 |
| rs774870088 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99426262 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 51455 |
| rs774893695 | snp | C/T | 1.64925e-05 | 0.00287158 | intron-variant | REV1 | GRCh38.p7 | 2:99462649 | GAAAAGGTAAACCAA[C/T]CACAAAGGTTACATT | 51455 |
| rs774900209 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99441745 | AATCCATGAAAAAAC[G/T]TATTAACAATTAAGA | 51455 |
| rs775049052 | snp | A/T | 3.36395e-05 | 0.00410105 | intron-variant | REV1 | GRCh38.p7 | 2:99434466 | GTGAGGAAAATATTA[A/T]ATTATTTCTGTATGT | 51455 |
| rs775076728 | snp | A/C/T | 0.000388647 | 0.0139355 | intron-variant | REV1 | GRCh38.p7 | 2:99442281 | AAAAAAAAAAACCAA[A/C/T]CAGCTTTGCAGTAAT | 51455 |
| rs775078007 | snp | G/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484114 | TTATCCTTAGCAAAC[G/T]AACACACGAACAGAA | 51455 |
| rs775091918 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476517 | GCCCAGATTGCGCCA[C/T]TGCACTCCAGGCTGG | 51455 |
| rs775119415 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99463013 | GAATTGCCTGAACCC[A/G]GGAGGTGGAGGTTGC | 51455 |
| rs775159436 | snp | A/T | 1.64988e-05 | 0.00287213 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439007 | GCAGTCTCTGAAATC[A/T]GTGCTGCTCTTCTCA | 51455 |
| rs775187386 | in-del | -/C | 0.000431329 | 0.0146792 | intron-variant | REV1 | GRCh38.p7 | 2:99442276 | AAAAAAAAAAAAAAA[-/C]CCAACCAGCTTTGCA | 51455 |
| rs775192522 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99443944 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC | 51455 |
| rs775230441 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482624 | CTCTTCCCAGGACTC[C/T]TAAGAGAATTAAATG | 51455 |
| rs775234607 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99424682 | GCACAGTTTGGCCAG[A/G]GTTCATCCCCCAAAG | 51455 |
| rs775260640 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99446789 | TGAGCTATCGCACCC[A/G]GCCGGAAAACACCAT | 51455 |
| rs775333740 | in-del | -/TAAAG | | | intron-variant | REV1 | GRCh38.p7 | 2:99409125 | ACATAAATAAGTTTT[-/TAAAG]TAAATAAATAAATGA | 51455 |
| rs775347017 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99431331 | ATGCTAGCTATACTA[C/T]TACAAATTAAAGACA | 51455 |
| rs775370047 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99479642 | AAAAAAAATAAAAAT[A/C]ATAAAAAGAGCCAGG | 51455 |
| rs775439094 | snp | A/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432377 | AGATTCTAATTCCTA[A/T]ACCGATCCTCAATAT | 51455 |
| rs775461112 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99427455 | TGTGACCCACATATA[A/C]ACATTCTACTTTGTA | 51455 |
| rs775472576 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99468685 | AACCTGCCAATCTCT[C/T]CTTATCCAGTAACTT | 51455 |
| rs775478404 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490517 | GGTACTGTGTGAAGA[C/T]GCGCCAGACGCCCGG | 51455 |
| rs775500793 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456979 | GAATTAGGACTAGAA[C/T]GTCTTTCTCCATTTT | 51455 |
| rs775560297 | snp | G/T | 1.65113e-05 | 0.00287322 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438936 | AAAGAATTAGTTCTG[G/T]GTGGATTCCGCAAAG | 51455 |
| rs775569337 | snp | C/G/T | 1.69553e-05 | 0.00291159 | intron-variant | REV1 | GRCh38.p7 | 2:99404720 | AAGTTAAAGCATGCT[C/G/T]AGAGATGAGGTGTTT | 51455 |
| rs775570530 | in-del | -/C | 1.64798e-05 | 0.00287047 | intron-variant | REV1 | GRCh38.p7 | 2:99403674 | TCTTCATTTTTGTTA[-/C]ATGCCACTTCCAAGG | 51455 |
| rs775587875 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406018 | CTTGTTAGTATCAGG[A/G]CTGGTCGGCAGATGT | 51455 |
| rs775589635 | snp | A/G | 1.68238e-05 | 0.00290028 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402595 | ATGTTCTCAAATCAT[A/G]AGACGACTACATCTC | 51455 |
| rs775617754 | in-del | -/AA | | | downstream-variant-500B, utr-variant-3-prime | REV1, EIF5B | GRCh38.p7 | 2:99400145 | CAAGAATTATCTTAC[-/AA]AAACTAAACTATCAT | 51455 |
| rs775629911 | in-del | -/T | 1.67374e-05 | 0.00289282 | intron-variant | REV1 | GRCh38.p7 | 2:99418987 | AAATAGTCACAATTA[-/T]TTTTTTAAATTTCTC | 51455 |
| rs775632716 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432066 | CTGGAAATCCAGGAA[A/G]GGGTAAAAGGCCCCA | 51455 |
| rs775637802 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404462 | TGAAAATGCTGGAAG[A/G]GCTATTAAATTTATT | 51455 |
| rs775653616 | snp | C/T | 1.65195e-05 | 0.00287393 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408100 | TTCCAATTATTTTTG[C/T]ATTATCTGTTGCCTG | 51455 |
| rs775674160 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480670 | TCCCTCAGAGCAACT[A/G]CAATTCAAAAATATA | 51455 |
| rs775707630 | snp | A/G | 1.71372e-05 | 0.00292717 | intron-variant | REV1 | GRCh38.p7 | 2:99406283 | CGTCTTTCCAAGGAC[A/G]TAAGCAGCACCTAAA | 51455 |
| rs775714497 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99454844 | TAAAACCAGACATAG[C/T]GACAGACAATTGAAA | 51455 |
| rs775716348 | snp | C/T | 1.69654e-05 | 0.00291246 | intron-variant | REV1 | GRCh38.p7 | 2:99449333 | TTAATAAATTAAACT[C/T]ACCTTTCCACAATCC | 51455 |
| rs775741713 | snp | A/G | 5.03368e-05 | 0.00501656 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410712 | GGCAATGTTATCACA[A/G]ATTCCATGGCCTCCA | 51455 |
| rs775766207 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99479610 | GCCTGAGCAACACAG[C/T]AAGACCTCATCTCTA | 51455 |
| rs775799892 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404560 | AAATTCCTGTATTAC[A/G]GCCATTTACTGGTTC | 51455 |
| rs775804526 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99455904 | CCCCTCCACCTGCTT[C/T]TTCACAAACTTCAGC | 51455 |
| rs775831035 | snp | G/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490977 | ATAATAGTCTTTATT[G/T]TTGTAATGCACAAAC | 51455 |
| rs775907424 | snp | C/T | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421580 | CATCAGGAGTAAGTT[C/T]GGTCTCTGCAAGGAT | 51455 |
| rs775908583 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442451 | TGGAATGTAGGAGAG[A/G]AGTCGTCCAGCTTTG | 51455 |
| rs775909470 | snp | C/G/T | 4.94271e-05 | 0.00497102 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442436 | GGTGTACAGCTGATA[C/G/T]GGAATGTAGGAGAGG | 51455 |
| rs775956926 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462862 | GGAAGCTGAGGCAGG[C/T]GGATCACCTGAGATC | 51455 |
| rs775965921 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99467342 | AATGTTTAAAACTTT[-/A]AAAAGGAAAAGGAAA | 51455 |
| rs775983669 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99424936 | TAAATCTGTGTGTCT[C/G]AGTGCCCCACATTAC | 51455 |
| rs776001444 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99427898 | GTCACCCCAATTATT[C/T]TGCAAGGCATGAAGC | 51455 |
| rs776016595 | snp | C/T | 1.68052e-05 | 0.00289867 | intron-variant | REV1 | GRCh38.p7 | 2:99434326 | TCAAAGAGAGCTCAT[C/T]TGTACCTGCTTTGCC | 51455 |
| rs776021048 | in-del | -/AC | | | intron-variant | REV1 | GRCh38.p7 | 2:99445479 | AATCTACAAGGATCA[-/AC]ACAAAATCAAGAACA | 51455 |
| rs776044861 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99464710 | TATTGTGCACTAGGC[A/C]TATTTATTTCCTCAG | 51455 |
| rs776045281 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460473 | TGATACCAAAATATA[C/T]ATATAGGCATTTTAC | 51455 |
| rs776063864 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462907 | AGCTTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 51455 |
| rs776071694 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410980 | TTACTCACTATCACG[C/T]TCAGCATCTATTAAA | 51455 |
| rs776085125 | snp | C/G | 7.70683e-05 | 0.00620711 | intron-variant | REV1 | GRCh38.p7 | 2:99403136 | ATATAAGATCCTCAA[C/G]AAAATGATAGTATGG | 51455 |
| rs776088270 | snp | C/T | 3.88644e-05 | 0.00440802 | intron-variant | REV1 | GRCh38.p7 | 2:99438536 | CAGAAATACCAATAA[C/T]AGCATAAGAGCAAAA | 51455 |
| rs776122490 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99478128 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51455 |
| rs776135347 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99459747 | AAAAAGGATAGAAGG[C/T]AAAGAAGTCAATCTT | 51455 |
| rs776135554 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99473646 | ACTTTATGTGTTTTT[A/T]TTACACCTTCAGCAT | 51455 |
| rs776158578 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99476367 | TCGAGACCAGCCTGG[A/C]CAACATGGTGAAACC | 51455 |
| rs776170038 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99441163 | TATTATTTGCTATAT[A/G]CCTTGATAGCACATT | 51455 |
| rs776178333 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438653 | CATTTTTTTTAACTT[C/T]TCCCTTCCTGGAAAG | 51455 |
| rs776213195 | snp | C/T | 1.69095e-05 | 0.00290765 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439291 | CATTTTCCGTTTCAA[C/T]CTTCTTAACGATGTG | 51455 |
| rs776278763 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448805 | CTCCACCTTCTCCCA[C/T]AACTGCTTCCTGACA | 51455 |
| rs776285200 | in-del | -/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416405 | ACTTCAGGACAGGAG[-/T]TAACAATGGAGAAGG | 51455 |
| rs776285473 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406381 | ACTTGGAAGACATCA[C/T]GGACAGAGTATGACC | 51455 |
| rs776290254 | snp | A/G | 0.000481612 | 0.0155104 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403034 | CTTTTTGGTGAACCA[A/G]TGGTTTTTTTCTTCT | 51455 |
| rs776290733 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant | REV1 | GRCh38.p7 | 2:99464994 | GGAGCTTCTGTATTG[A/G]GGAGGAAAAAAAAAA | 51455 |
| rs776413764 | snp | C/G/T | 3.29768e-05 | 0.00406048 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438829 | TGCTAAACGTAGATA[C/G/T]TGAAGAAGTGCTTTT | 51455 |
| rs776434396 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99488017 | ACAAACGAGAAAAAA[A/T]CAGAGATACTAGTAA | 51455 |
| rs776477054 | snp | C/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432588 | ACGTGAAAAGGCTTA[C/G]GATATAAAAGTAAAT | 51455 |
| rs776481455 | snp | A/T | 5.18318e-05 | 0.0050905 | intron-variant | REV1 | GRCh38.p7 | 2:99402223 | ATTTTTTCCCATTTG[A/T]TAAAAGTGATGAATT | 51455 |
| rs776482735 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456067 | AGCACTCACTCCCCC[C/T]GGGCAGCTTTCACAA | 51455 |
| rs776484686 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99418541 | ACTGAAAGTCAATTT[C/T]ATCATCCTCCCTTTT | 51455 |
| rs776508370 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456603 | AGGGATTACTATACA[G/T]AAAACAGGCTTCCTA | 51455 |
| rs776548176 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99405720 | TCTTTGCAAAAGCAC[-/TT]TTTCACTCAACCCAA | 51455 |
| rs776568119 | snp | A/C | 1.65529e-05 | 0.00287683 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405937 | CGGGACCTCTATACT[A/C]AGGTTAAGTCTCGAC | 51455 |
| rs776572865 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99420239 | TTATTTTCTGTATCT[C/T]GCAGTGTTTTGAAAT | 51455 |
| rs776599838 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99469784 | TCTGCTTTCTTTTTA[A/C]TATAGTTATTGGTAG | 51455 |
| rs776605958 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99479460 | AATTTACTATAATCT[A/G]TAGTTTTCAAGGTGA | 51455 |
| rs776609944 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99446863 | CAACTCTCCTCCTGT[-/C]CCACAGAAATTCCCC | 51455 |
| rs776661188 | snp | A/C | 5.82191e-05 | 0.00539501 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402389 | GGACCAGTCTTTTTG[A/C]AGGAGAAAGTCAGAG | 51455 |
| rs776662802 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99406785 | CTGTATTCCACTGAT[A/G]TTCTCGTCAACTAAG | 51455 |
| rs776667456 | snp | C/T | 8.24246e-05 | 0.00641915 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424204 | TATATGCATGAAAAT[C/T]GTATGGAACAGCTTG | 51455 |
| rs776706983 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99468490 | TAAACCTACTCACTA[A/C]GAAGTGACTGCCCTG | 51455 |
| rs776715603 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480592 | ATTCCACCCACACAA[G/T]TCATTAGATCTCTGA | 51455 |
| rs776760606 | snp | C/T | 1.65206e-05 | 0.00287403 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99408080 | AAACATGTTTAGCAT[C/T]GCCTTTCCAATTATT | 51455 |
| rs776761880 | snp | A/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412837 | AACCTATAAAGCATC[A/T]GACCTGTTTTGGGAC | 51455 |
| rs776761927 | snp | A/C/T | 1.91628e-05 | 0.00309532 | intron-variant | REV1 | GRCh38.p7 | 2:99405861 | TGTATTTTTGTATTT[A/C/T]TATTTAGGAGTATAA | 51455 |
| rs776780659 | snp | A/C | 1.66026e-05 | 0.00288115 | intron-variant | REV1 | GRCh38.p7 | 2:99442307 | GTAATCCCCAACTAG[A/C]CAAACTTACACCCTG | 51455 |
| rs776783597 | snp | A/G | 3.3024e-05 | 0.00406336 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438912 | TTACTGTGCAAAGGT[A/G]ATAATGAGAAAGAAT | 51455 |
| rs776796453 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99466630 | AACAATTTGAATTTT[C/T]ACTGTCACCCTTAAA | 51455 |
| rs776841445 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414141 | GCCTAGGTGACAGAA[C/G]AAGACCCTGTGTTTA | 51455 |
| rs776848318 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99441360 | AGCAAGCAATTTAAT[A/G]AATAAAGAGAAGGCT | 51455 |
| rs776936205 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99442971 | AACTACCATGTACAT[C/G]CTCACAGCATATCAC | 51455 |
| rs776939529 | snp | A/T | 1.6966e-05 | 0.00291251 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410702 | GAGCTTACCTGGCAA[A/T]GTTATCACAAATTCC | 51455 |
| rs776945135 | snp | A/T | 4.94368e-05 | 0.00497152 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402730 | GGTGCTGGAGGTCTC[A/T]CACAGCCAGCTGGGT | 51455 |
| rs776950764 | snp | C/T | 3.34577e-05 | 0.00408995 | intron-variant | REV1 | GRCh38.p7 | 2:99424303 | GAGAACAAAACACAA[C/T]GGAGGTTATTCTAGG | 51455 |
| rs776990952 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99470915 | AAATTTATGTTCAAG[G/T]GCTACTTCTTTACAG | 51455 |
| rs777028137 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99444176 | AATCTTTGTTCTGTG[G/T]TATTATGTATATCAA | 51455 |
| rs777028330 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428131 | TAAAGGGAGAGACCC[C/T]GCAGAGGCAGCCTTA | 51455 |
| rs777059714 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99430160 | CAGATAAAAACTTAT[-/AA]TAAATTCAAAGTGTC | 51455 |
| rs777070534 | snp | C/G/T | 4.94575e-05 | 0.00497259 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435878 | ACTGATACAAAGAAG[C/G/T]AATCCATATCAACAT | 51455 |
| rs777096073 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99472399 | GTTGCGGGTGGAGTT[A/G]CTGTTTAACAGGTAG | 51455 |
| rs777155046 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99465658 | ATTCATAAAAAGAGG[-/C]TAAATGAAACCCCTT | 51455 |
| rs777163992 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99452484 | AACATCATGAAAGCT[A/G]TATGACATTAAACAT | 51455 |
| rs777210484 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99401939 | TTTCAGTAGAGATGG[A/G]GTTATGCCATTTTGG | 51455 |
| rs777212258 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403767 | CATACGCTGCTTTCA[A/G]CTCCCTCTGAAGTTC | 51455 |
| rs777212771 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99462765 | GATGACCTCATAAAC[A/G]TAAACCATAAGGCAA | 51455 |
| rs777250425 | snp | C/T | 1.65957e-05 | 0.00288055 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438638 | AGACCTGCCTGTTTT[C/T]ATTTTTTTTAACTTT | 51455 |
| rs777259410 | snp | A/G/T | 8.94664e-05 | 0.0066878 | intron-variant | REV1 | GRCh38.p7 | 2:99449328 | TAAATTTAATAAATT[A/G/T]AACTTACCTTTCCAC | 51455 |
| rs777306820 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99457493 | TCGAGACCAGCCTGG[C/G]CAACATGGCGAAACC | 51455 |
| rs777314954 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99443736 | TGTTTTACCAAAATT[C/G]AGGTTACATTCAAAA | 51455 |
| rs777315177 | in-del | -/ACA | 8.33521e-05 | 0.00645516 | cds-indel, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438612 | CTACCTGTGTCAGTT[-/ACA]ACAAGTGCAGACCTG | 51455 |
| rs777387504 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99401522 | GAGGCCGAGGAGGGC[A/G]GATCACCTGAGGTCA | 51455 |
| rs777413897 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415324 | AGAATCAAATCTCAA[C/T]GAAGAGAGAGTCAAG | 51455 |
| rs777449703 | snp | C/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421570 | TTTGCAAATTCATCA[C/G]GAGTAAGTTTGGTCT | 51455 |
| rs777474552 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466220 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTAAG | 51455 |
| rs777492721 | in-del | ATC/TCAAAATAAAACA | | | intron-variant | REV1 | GRCh38.p7 | 2:99453917 | AAAAAAAAAAAAAAA[ATC/TCAAAATAAAACA]AAACTAGATTCAGGG | 51455 |
| rs777510114 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99464426 | CTATTCATTAAAACT[C/T]TGGGGTGTTGTTTTC | 51455 |
| rs777525345 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403704 | GCTCACCAGATGCGC[C/T]GGCTGACTGCTGGTG | 51455 |
| rs777526632 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438789 | TTGCAGTCTGAAGGT[C/T]TGGATGGCACTGAAG | 51455 |
| rs777527018 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462529 | AGATGGCAACTCCAC[C/T]AAAAATTGTAGATGA | 51455 |
| rs777539590 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99442721 | TTACCACCCTGTCAA[A/C]AGTTAACAGAGAATC | 51455 |
| rs777569976 | snp | A/G | 1.65168e-05 | 0.00287369 | intron-variant | REV1 | GRCh38.p7 | 2:99401366 | GCCTAAAGGTGGGGA[A/G]AGAAGAAATGTCATT | 51455 |
| rs777606482 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99450582 | ATACCAGGTTTGTCT[A/G]AATTTTACAGCACAA | 51455 |
| rs777631792 | snp | C/T | 1.76235e-05 | 0.0029684 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406456 | GTGGAAGGGTTCAGA[C/T]TAGTTGGAACCAACT | 51455 |
| rs777644141 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99416356 | TCCTATATGAAACCC[C/G]TTTTTAAAGGAACAG | 51455 |
| rs777666127 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481228 | AATTACGTACATCTA[A/G]AAGTACAAATTCAAG | 51455 |
| rs777687269 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405994 | ATTCCATTTCCCTGA[A/G]GACTCAGCCTTGTTA | 51455 |
| rs777694649 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99451732 | ACTAGAACTCCTTTC[A/G]AGTAATGTATATGAC | 51455 |
| rs777701192 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99461335 | CACTGTAGAGGCACT[A/C]AGGATATAGTGATGA | 51455 |
| rs777703692 | snp | C/T | 3.30147e-05 | 0.00406279 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438895 | CACCATTGATTTTAG[C/T]GTTACTGTGCAAAGG | 51455 |
| rs777755607 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480398 | TGGCCAGATGTAGAG[A/G]TAGACAAACTAAGGT | 51455 |
| rs777771050 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410553 | CTGAATGCCTTGGGC[A/T]GATGCCTGCTTCTAC | 51455 |
| rs777791356 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99460119 | TTTTCACTCTATCGC[C/G]AGGCTGGAGTGCAGT | 51455 |
| rs777833737 | in-del | -/TGTT | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | REV1, EIF5B | GRCh38.p7 | 2:99400674 | AAGTGGGTGTGAGGG[-/TGTT]TGTTTCTAATTCAAA | 51455 |
| rs777857024 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99472221 | ACGAAATACTATTCA[A/G]CCTTAAAAGGAAGGA | 51455 |
| rs777869036 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407262 | ACCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 51455 |
| rs777875842 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99409601 | GTAATCCCAACACTA[A/T]GGGAGGCTGCGGTGG | 51455 |
| rs777877668 | snp | A/G | 1.68653e-05 | 0.00290385 | intron-variant | REV1 | GRCh38.p7 | 2:99412974 | AGGGAATATAGTTAA[A/G]TATGCAGAATAAGCT | 51455 |
| rs777891716 | snp | A/C | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402692 | TCTTCACATCATTGA[A/C]TTCAACAGCTCCAGC | 51455 |
| rs777892720 | in-del | -/TATAAC | | | intron-variant | REV1 | GRCh38.p7 | 2:99479521 | TATCAGAGATTTGCA[-/TATAAC]TATAATATGAGATCT | 51455 |
| rs777943212 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99484942 | GTGCCAACCTTATAC[A/G]GTAGCTGTAGATATT | 51455 |
| rs777987124 | snp | A/C/G | 3.29534e-05 | 0.00405904 | missense, synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412821 | ATCCAAGCCACGGCA[A/C/G]AACCTATAAAGCATC | 51455 |
| rs777991021 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432282 | CTAAGGATGCTATTT[A/G]TCCTAATACTTTGTC | 51455 |
| rs777997527 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99432590 | GTGAAAAGGCTTAGG[-/AT]ATAAAAGTAAATGAC | 51455 |
| rs778012841 | snp | C/T | 3.29571e-05 | 0.00405924 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99464965 | CGCTTCCTCCATCCA[C/T]CTCGCCTCATGGTGG | 51455 |
| rs778055009 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99486902 | ACAAGTCTAAGGGGG[C/G]AAATAAATAAGTGGG | 51455 |
| rs778066283 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433493 | TCCTCAGAGATGTTC[A/G]CTGGCTTTCCTTTTG | 51455 |
| rs778073673 | snp | C/G | 1.69663e-05 | 0.00291253 | intron-variant | REV1 | GRCh38.p7 | 2:99435801 | TTTATAACAATATAT[C/G]AGTTTTCTTAAAACA | 51455 |
| rs778085440 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447320 | TGGGACTACAGGCGC[A/G]CGCCACCACGCCCAG | 51455 |
| rs778089217 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99422683 | TTTCCCAAGGGTGGT[-/A]GAAGAACACTACTGT | 51455 |
| rs778142341 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99452001 | TCTCTGGTTCTATTT[A/C]TTCAATACTAGAACA | 51455 |
| rs778143842 | in-del | -/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99455847 | CTTGCATATTCCCCC[-/TT]GTTTCATTTTGTGAA | 51455 |
| rs778145917 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99474688 | AGGCGAATCACATGA[G/T]ATCAGAAGTTTGAGA | 51455 |
| rs778151581 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437068 | ATCTGCAACCTCAAC[C/T]CCTAGGGCTCAAACA | 51455 |
| rs778177929 | in-del | -/GTTA | | | intron-variant | REV1 | GRCh38.p7 | 2:99433964 | AAAGTTCTACTGTTT[-/GTTA]GTTATTCTACTTCCT | 51455 |
| rs778185587 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99448942 | AGTGTTGTTTAAGAC[A/G]TTATTTTTCACCCTG | 51455 |
| rs778248191 | in-del | -/TA | 6.92737e-05 | 0.0058849 | intron-variant | REV1 | GRCh38.p7 | 2:99408017 | AATTTACAATGTTAC[-/TA]TATATACTTACCCCT | 51455 |
| rs778268161 | in-del | -/TTC | 1.84517e-05 | 0.00303735 | cds-indel, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403058 | TTCTTCTTGTTTCTT[-/TTC]TTTTCTTTCACTGCT | 51455 |
| rs778278318 | snp | A/G | 0.000141006 | 0.00839544 | intron-variant | REV1 | GRCh38.p7 | 2:99410671 | GAAATATAATTACCA[A/G]TATCATTTCTGAGGT | 51455 |
| rs778288620 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99455440 | TCACCACAATCAACT[A/G]AAAGCCACGGATACA | 51455 |
| rs778301977 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438981 | GTGCTTTGCTGCAAC[C/T]GCTGCAGAGTGCAGT | 51455 |
| rs778340647 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467788 | TGGTGGCTCACCCCT[A/G]TAATCCCAGCACTTT | 51455 |
| rs778349400 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99417998 | TCGTTTTAAGTTATA[C/T]ACTACGGGGGTCAGG | 51455 |
| rs778366333 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99415470 | TATCCAATACAGACA[C/T]AGAGGAGTAAACTTC | 51455 |
| rs778378077 | in-del | -/ATT | | | intron-variant | REV1 | GRCh38.p7 | 2:99444773 | TATATAGACAGAAAC[-/ATT]ATCTGAAAGCATATT | 51455 |
| rs778391084 | snp | A/G | 4.97863e-05 | 0.00498906 | intron-variant | REV1 | GRCh38.p7 | 2:99418966 | TTAAAAAAAAAAGTC[A/G]TCCAAGAAATAGTCA | 51455 |
| rs778393907 | snp | C/G | 2.06247e-05 | 0.00321122 | intron-variant | REV1 | GRCh38.p7 | 2:99429797 | TATAAAAATAATTAA[C/G]CAAATTATTCATTAA | 51455 |
| rs778432435 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480177 | ATTTGTTTTTAATTA[G/T]CCAGTCATGGTGGTG | 51455 |
| rs778455488 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430768 | TTTGCCACCTTTAGC[C/T]TCACTAGTAATTGAG | 51455 |
| rs778461211 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99453763 | CTGGGCATGGTAACA[C/T]GCGCCTGTAGTCCCA | 51455 |
| rs778470331 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99416106 | AACATTTATGGGTAC[-/A]AAGGGACTAAAGAGG | 51455 |
| rs778547331 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416271 | TTTAACAAAGATAAA[C/T]AGGTTTCTTTTCTAA | 51455 |
| rs778569116 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99437995 | ATAAAAAAATCCTAT[A/G]ATCTGTAAAAGGAAC | 51455 |
| rs778570779 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99489452 | GGAGTTTGCGGCGCG[C/G]TCTGACCGGGCCGGC | 51455 |
| rs778587326 | snp | C/T | 3.32204e-05 | 0.00407542 | intron-variant | REV1 | GRCh38.p7 | 2:99435970 | GACAGCATTCAAACC[C/T]CAAGCTAATTTTTAC | 51455 |
| rs778652228 | snp | A/G | 0.000115629 | 0.0076027 | intron-variant | REV1 | GRCh38.p7 | 2:99404397 | AAGTTGGAGCAGGGG[A/G]GTGAGAATATTGAAA | 51455 |
| rs778652306 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410781 | CATGATTTTGAGAGT[C/T]AGACGTTTACCCTTC | 51455 |
| rs778665764 | snp | C/T | 2.02616e-05 | 0.00318283 | intron-variant | REV1 | GRCh38.p7 | 2:99449515 | AGGATCTGCAAAATT[C/T]ATATTAAAATATATT | 51455 |
| rs778719683 | snp | A/T | | | | | GRCh38.p7 | 2:99421790 | ATTGGCTGAAGTACC[A/T]TTTTAGTCACCCAAC | 51455 |
| rs778724236 | in-del | -/TAAG | | | | | GRCh38.p7 | 2:99421284 | CCAATTTTTTAAGAA[-/TAAG]TAAGAAATATTCTAA | 51455 |
| rs778739102 | snp | A/G | 6.60578e-05 | 0.0057467 | | | GRCh38.p7 | 2:99406348 | TGCTCCTCTTCGGTG[A/G]ATTTCTTAGCTTTCT | 51455 |
| rs778827019 | snp | A/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412806 | TCGAACTGGTCTATC[A/T]TCCAAGCCACGGCAG | 51455 |
| rs778827242 | snp | A/G | 2.26488e-05 | 0.0033651 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403084 | CACTGCTGCCTTTAG[A/G]TGAAGTAAAGGATTC | 51455 |
| rs778830109 | snp | A/C/T | 9.90694e-05 | 0.00703747 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438925 | GTGATAATGAGAAAG[A/C/T]ATTAGTTCTGTGTGG | 51455 |
| rs778838383 | snp | C/T | 1.65337e-05 | 0.00287517 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439258 | CATTCCAACTGTTCA[C/T]GCCATTGACTTTGAC | 51455 |
| rs778870331 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411633 | AGGCTGGTCTCCAAC[A/T]CCTGACCTCAGGTGA | 51455 |
| rs778907207 | in-del | -/AAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99476556 | CAAGAATCTGTCAAT[-/AAT]AATAATAATAATAAT | 51455 |
| rs778920143 | snp | C/T | | | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424208 | TGCATGAAAATCGTA[C/T]GGAACAGCTTGAAGA | 51455 |
| rs778927382 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99410608 | AGGTCTTTATTCAAA[C/T]TCCTCCTTGGTTTTC | 51455 |
| rs778949017 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99447397 | GGATGTTCTCGATCT[C/T]TTGACCTCGTGATCT | 51455 |
| rs779020688 | snp | A/G | 1.68244e-05 | 0.00290033 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405916 | AAAATGTACCTGGGA[A/G]GGTGACGGGACCTCT | 51455 |
| rs779027036 | snp | A/C | 1.6492e-05 | 0.00287154 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434407 | CAGGACGTAAAGGTG[A/C]CCTTCCTGTGCCTCT | 51455 |
| rs779110834 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99464039 | GTCCTCCCTACACAT[A/G]GGAAAGAATACAATG | 51455 |
| rs779145394 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431871 | ACTGCTCATCAAAAC[C/T]TGACAAACTAGACGG | 51455 |
| rs779199243 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99477379 | CCATGGGAATAAGGA[A/C]AATACCCTATGGAAG | 51455 |
| rs779205633 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99420872 | GGCAAGAAAAGGGGT[A/T]TCTTGCCAGAAGGTA | 51455 |
| rs779209050 | in-del | -/A | 0.042547 | 0.139511 | intron-variant | REV1 | GRCh38.p7 | 2:99418953 | ATATTAGAACCTATT[-/A]AAAAAAAAAGTCATC | 51455 |
| rs779212144 | snp | A/C | 2.30502e-05 | 0.00339479 | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439348 | AGTTAATAATATCTG[A/C]CTTTTAGGTTAAAAC | 51455 |
| rs779216662 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99433744 | TAATTTCTAAGAAAA[C/T]ATTTCTCAGTGAATT | 51455 |
| rs779216863 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412743 | TACCTGAGTAAACCT[C/T]ATTCCATAGTTGATC | 51455 |
| rs779228114 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456495 | CGTAAAAAGGTAACA[C/T]TTGAGCAGAGATCTG | 51455 |
| rs779279616 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460007 | ACACCACAGCTTCTT[C/T]TACAGTGAAAACTGC | 51455 |
| rs779295439 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99473891 | TATTCCTTCATCACT[A/G]ACTTGTGTTTATACA | 51455 |
| rs779302617 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99419863 | AAGACTTATATTGAG[A/G]ACATATCTTGGTTTT | 51455 |
| rs779318152 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442360 | TGCTTGGACCTGGCA[A/G]AGGATCCTCAGGTCT | 51455 |
| rs779327160 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99470490 | AAACATCTGCTAGCC[A/G]TAATAAAGAAATCAA | 51455 |
| rs779395114 | snp | G/T | 1.66974e-05 | 0.00288936 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402358 | GGATCTAGGAAGGGG[G/T]AAAAACTTCAAATGA | 51455 |
| rs779415803 | snp | C/T | 1.65787e-05 | 0.00287907 | synonymous-codon, stop-gained, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99424280 | CTTAATGCCAAGTTG[C/T]CTAGAGCGAGAACAA | 51455 |
| rs779427509 | snp | A/C | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99405976 | GACAGGAGTATGTAG[A/C]CCATTCCATTTCCCT | 51455 |
| rs779478037 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478756 | AGGGCCTGTTAAAAC[A/G]CAAGATGCTGGGCCC | 51455 |
| rs779524194 | snp | G/T | 1.6504e-05 | 0.00287258 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438875 | CTGAACAGTGGAGTG[G/T]TGAGCACCATTGATT | 51455 |
| rs779568742 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99446906 | GCCTAACTATTGCCC[C/T]CAGATAAAAACTCTA | 51455 |
| rs779570892 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99407761 | ACTTCTAGGAAACAA[A/G]AACAGGGAAGACATG | 51455 |
| rs779591880 | snp | A/G | 0.000100836 | 0.00709984 | intron-variant | REV1 | GRCh38.p7 | 2:99403861 | CTGAGCTAATTGTAG[A/G]TGGTAGCTGGTTTCT | 51455 |
| rs779600336 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440545 | TGACAGGCAACTGTG[A/G]GTAGATGCCATGCTC | 51455 |
| rs779602759 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99403732 | GTGAGTGCTGTTCTC[A/G]CCCTGCCTTTGTCTT | 51455 |
| rs779606417 | snp | G/T | 0.000610314 | 0.0174581 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435837 | AAGAATACAGACCTT[G/T]GAGATCTGGTCTATT | 51455 |
| rs779692300 | snp | A/G | 4.95511e-05 | 0.00497726 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439191 | TTCTGTTTCCTTCCC[A/G]GAGAGGTCTGCTCCA | 51455 |
| rs779722392 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442379 | ATCCTCAGGTCTGCA[C/T]ACAGGATTAAAGCTG | 51455 |
| rs779751733 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99477828 | TGATTTAACAAAATC[A/G]ATAGTTAATACAAAC | 51455 |
| rs779759581 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469648 | ATGTTCAAAACTCTA[C/T]CAAGAGTCTCATCAA | 51455 |
| rs779793005 | snp | C/T | 1.6495e-05 | 0.0028718 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435938 | TTCAATACTGACATA[C/T]CTCCTAGAAGGAAAA | 51455 |
| rs779794147 | snp | A/C | 1.74163e-05 | 0.00295091 | intron-variant | REV1 | GRCh38.p7 | 2:99408009 | CAAAGTCAGAATTTA[A/C]AATGTTACTATATAC | 51455 |
| rs779796057 | snp | C/T | 0.000134382 | 0.00819589 | intron-variant | REV1 | GRCh38.p7 | 2:99424946 | TGTCTCAGTGCCCCA[C/T]ATTACCTTTGACATT | 51455 |
| rs779810297 | in-del | -/TCCT | | | intron-variant | REV1 | GRCh38.p7 | 2:99466049 | GGGTTCACACCATTC[-/TCCT]TCCTGCCTCAGACTC | 51455 |
| rs779845069 | in-del | -/C | 8.7447e-05 | 0.0066118 | intron-variant | REV1 | GRCh38.p7 | 2:99402214 | GACATGCCATTTTTT[-/C]CCCATTTGATAAAAG | 51455 |
| rs779863432 | in-del | -/TC | | | intron-variant | REV1 | GRCh38.p7 | 2:99468177 | AAGAGCGAAACTCCA[-/TC]TCAAAAAAAAAAAAA | 51455 |
| rs779868491 | snp | C/G | 8.24355e-05 | 0.00641957 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99421529 | CAGCACATTTCGTCT[C/G]GTCTTTGATTTCCAT | 51455 |
| rs779954369 | snp | C/G | 4.95946e-05 | 0.00497944 | synonymous-codon, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406344 | TTTGTGCTCCTCTTC[C/G]GTGGATTTCTTAGCT | 51455 |
| rs779958343 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426923 | GTGCGGTGGCTCACT[C/T]CTGTAATCCCAGCAC | 51455 |
| rs779962038 | snp | C/T | 2.59239e-05 | 0.00360017 | intron-variant | REV1 | GRCh38.p7 | 2:99406137 | ATATAAAATAGCCTC[C/T]TCAGATCATCGGGCA | 51455 |
| rs779977228 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99449254 | TGGGCGACAAAGCGA[G/T]ACCCTATCTCAAAAA | 51455 |
| rs779985572 | in-del | -/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99479299 | CTACTGCACTCCAGC[-/G]CTGGGTGACAGAGCG | 51455 |
| rs780047948 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462039 | ATTCAGGTCCTTTCC[C/T]TCCCTGCTTGGCGAC | 51455 |
| rs780053996 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99411962 | TATCCAGCCGGGCGC[A/C]GTGGCTCACATCTGT | 51455 |
| rs780055423 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483600 | GCCTATATGAGAAAG[C/T]ATCATTTTCAACTGC | 51455 |
| rs780074565 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99448593 | CATTATCTTGATGTA[G/T]TACCATGCTAAAAAC | 51455 |
| rs780087290 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99434121 | ATACAAAGCAAATCA[A/G]TCATATCTTGTAAAA | 51455 |
| rs780099826 | snp | A/T | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410824 | TCTAGTCTTCTTTGA[A/T]TTTCTTCTGAAAGAC | 51455 |
| rs780105985 | snp | A/C | 1.71534e-05 | 0.00292855 | intron-variant | REV1 | GRCh38.p7 | 2:99434286 | ATAGCAAAATCCAGA[A/C]GCCATCCACAGGAGC | 51455 |
| rs780143847 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456022 | CCAATCTCACACCAC[G/T]AAAGTGCAACCACTG | 51455 |
| rs780193732 | snp | C/T | 1.6507e-05 | 0.00287284 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439228 | CAAAACTAAAATCAT[C/T]ATTTTCATCTTCTTC | 51455 |
| rs780203722 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426416 | TTACAATATTTTCAT[A/T]TTCAAAACATTAATT | 51455 |
| rs780222947 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99477104 | TCCACGATGGCAAAA[C/T]GGCACTGTCCTCCAG | 51455 |
| rs780268577 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99421091 | TGGAGTCAGGGTGAC[C/T]TCTAGAACTGAGTGA | 51455 |
| rs780277971 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99458262 | AAAAATACTAAATCC[A/C]ATTAGAAAATGAGGA | 51455 |
| rs780286109 | snp | C/T | 1.65143e-05 | 0.00287348 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439087 | TGTTGACCATGGGCA[C/T]CAAGCAATCCTGTGT | 51455 |
| rs780288168 | in-del | -/CCATTGA | 1.65348e-05 | 0.00287526 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439260 | TTCCAACTGTTCATG[-/CCATTGA]CTTTGACTTCATTTT | 51455 |
| rs780307429 | snp | C/T | 1.77228e-05 | 0.00297676 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99429945 | GATGAATCTGGTATA[C/T]CTGCTTTAAAAATAA | 51455 |
| rs780345242 | snp | A/G | 8.18967e-05 | 0.00639857 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402330 | CACAACTTGGAGAAT[A/G]TCTTCTTCCATTGGA | 51455 |
| rs780356570 | snp | C/G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99422360 | TAAGAAATCACAAAA[C/G/T]AGAACTGGACCAGAA | 51455 |
| rs780366349 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99428887 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 51455 |
| rs780427542 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99408137 | AGTTACAGTCCTGTA[A/G]GTGATAGAATTAAAA | 51455 |
| rs780432511 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99462285 | ACCTCACGTGACTTT[C/T]TGAAACTATGTACTT | 51455 |
| rs780443790 | snp | A/G | 3.30868e-05 | 0.00406723 | intron-variant | REV1 | GRCh38.p7 | 2:99401376 | GGGGAGAGAAGAAAT[A/G]TCATTAGGAATTAGG | 51455 |
| rs780449296 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99429472 | GGAAGTATGGATTAC[A/T]AGATTTTTTCTTAGC | 51455 |
| rs780463215 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99456797 | TATCTGGATCTTAAT[G/T]AATGAATATACTTCC | 51455 |
| rs780478841 | snp | C/G | 0.000115669 | 0.00760402 | intron-variant | REV1 | GRCh38.p7 | 2:99412725 | AATCTGTTCAATGAT[C/G]AGTACCTGAGTAAAC | 51455 |
| rs780522540 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99461646 | GAATCCCCAAGAAAA[C/T]AGAGAAAAATTTAGG | 51455 |
| rs780522577 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99476086 | GCAACTTTACGTAAC[C/T]TTTTCTATGCTTGCC | 51455 |
| rs780549205 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438804 | TTGGATGGCACTGAA[A/G]GTGCTGCCTTGCTAA | 51455 |
| rs780568040 | in-del | -/AAAAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99454557 | CTCCAGCTCAAAAAA[-/AAAAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs780610277 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99475175 | CAAGGAACAAAGGAG[A/T]CAGGGTCATTTATAA | 51455 |
| rs780638082 | snp | A/G | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404650 | CCCGGAGATCAGGTG[A/G]AAGTGCTTCTAAAAC | 51455 |
| rs780645801 | snp | A/G | 3.32939e-05 | 0.00407993 | intron-variant | REV1 | GRCh38.p7 | 2:99424105 | TCTTTACTATTAGCT[A/G]AAAGAAGGAAAACAC | 51455 |
| rs780651646 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99443157 | CTGAGTTATATATGG[-/C]TACTCTACCTTTAAA | 51455 |
| rs780664746 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99440598 | GGGAAAAAGACAAAG[C/T]AGATATGATTAAAAG | 51455 |
| rs780709195 | in-del | -/G | 0.000134968 | 0.00821375 | intron-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99402354 | CATTGGATCTAGGAA[-/G]GGGGAAAAACTTCAA | 51455 |
| rs780715295 | in-del | -/GTAT | 8.62751e-05 | 0.00656735 | intron-variant | REV1 | GRCh38.p7 | 2:99406509 | AACCCAGAATAAAGA[-/GTAT]GTATGCTTCTAGGAA | 51455 |
| rs780717812 | snp | A/G | 1.75434e-05 | 0.00296165 | intron-variant | REV1 | GRCh38.p7 | 2:99407988 | AAAAATGAGAGATAC[A/G]TTACACAAAGTCAGA | 51455 |
| rs780727236 | snp | G/T | 1.94426e-05 | 0.00311784 | missense, nc-transcript-variant, intron-variant | REV1 | GRCh38.p7 | 2:99406471 | TTAGTTGGAACCAAC[G/T]GATTCACGTGAATCC | 51455 |
| rs780729390 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99427166 | CAGCCTGGGCAAAAG[A/G]GCAAGACTTCATCTC | 51455 |
| rs780739141 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99467676 | ATCAGAACCCTATGA[A/G]TAACAAGAAATTGGA | 51455 |
| rs780740052 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99466383 | GAGTAGCTGGGATTA[C/G]AGGCACCTGCCACCA | 51455 |
| rs780745137 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99462554 | AGATGAAGTCCCATC[C/T]TTCTGCATAGCAGCA | 51455 |
| rs780748269 | in-del | -/AA | | | intron-variant | REV1 | GRCh38.p7 | 2:99444807 | GTATAAGACCTTTTT[-/AA]AAATCTCTCTGGGAT | 51455 |
| rs780788860 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482408 | ACCAAATTATCAAAC[A/G]TGAGGTGTAGTGGGA | 51455 |
| rs780806643 | snp | A/G | 0.000117713 | 0.00767091 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99406077 | TTCTAGAAGCAGATG[A/G]TATTTCCAGATCCAC | 51455 |
| rs780812326 | snp | C/T | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99491634 | GCAACACCAGGAGGT[C/T]ATCTGCTGAGATGCT | 51455 |
| rs780817096 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99413379 | TGATTTCGGTCATCA[A/C]CAAATCTCACAGTGG | 51455 |
| rs780828091 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99426071 | TGTTTATAGTCCAGG[C/T]GCGGTGGTACACATC | 51455 |
| rs780879310 | in-del | -/AT | | | frameshift-variant, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99412882 | AGTTTTGCCATGGTC[-/AT]ATACTGCAAGTCTCC | 51455 |
| rs780882537 | in-del | -/CATT | | | intron-variant | REV1 | GRCh38.p7 | 2:99465263 | GAGCACCAATCCTAA[-/CATT]CACTTACATAAAACA | 51455 |
| rs780928985 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438850 | AAGTGCTTTTTGTGC[C/T]TGAAGGCCCCTGAAC | 51455 |
| rs780930698 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99416692 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 51455 |
| rs780950064 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99442362 | CTTGGACCTGGCAGA[A/G]GATCCTCAGGTCTGC | 51455 |
| rs780990744 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99481471 | TGTTCCAATTTTTAA[C/T]ACAACAGAGGTAACT | 51455 |
| rs781019412 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99451449 | GCTCTTTGAAGTTCA[C/T]TTCTGAAAGCTCTTA | 51455 |
| rs781037930 | snp | A/T | 1.65097e-05 | 0.00287308 | intron-variant | REV1 | GRCh38.p7 | 2:99435830 | CATAAGCAAGAATAC[A/T]GACCTTTGAGATCTG | 51455 |
| rs781038692 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99435912 | TTATACAGCTCTGAT[A/G]TCTGGGAGAATTCAA | 51455 |
| rs781072994 | in-del | -/GGCCCTTCATT | | | intron-variant | REV1 | GRCh38.p7 | 2:99415822 | GAATGAGGTGCAGAG[-/GGCCCTTCATT]GAAGAGTGCATGCGC | 51455 |
| rs781099459 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99462055 | TCCCTGCTTGGCGAC[A/C]CAAATGCTGGCAGTT | 51455 |
| rs781105507 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439889 | ACATTAAATCTAATA[C/T]GAAACCAGATGGTTT | 51455 |
| rs781107371 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99437141 | CGTGCCACCACGCCC[A/C]GCTAATTTTTTTTTT | 51455 |
| rs781125570 | snp | C/T | 0.000150619 | 0.00867679 | intron-variant | REV1 | GRCh38.p7 | 2:99418783 | AGATATGAAAAGTAC[C/T]TGTAATGCCTGTAAT | 51455 |
| rs781142504 | snp | A/T | 1.65381e-05 | 0.00287555 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99434432 | GCCTCTGTTACTTGT[A/T]ACAGCCACTGGTTTT | 51455 |
| rs781183244 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469034 | TCAGAGTGAGTCTAA[C/T]AGCACTGAGCCTAAC | 51455 |
| rs781212915 | in-del | -/ATT | | | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401142 | TAAAAGAAATTTAAA[-/ATT]ATTATAAAAACTCCG | 51455 |
| rs781214914 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99435594 | CAGATCCTGCCTACA[C/T]TAGTCTTCGATGACA | 51455 |
| rs781219058 | snp | A/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99485349 | CATTATGAAAAGAAC[A/T]GAAAGATACAGAGCA | 51455 |
| rs781231778 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99439074 | CTGCTGGCAACACTG[C/T]TGACCATGGGCACCA | 51455 |
| rs781233458 | snp | A/T | 7.13051e-05 | 0.00597055 | intron-variant | REV1 | GRCh38.p7 | 2:99429816 | ATTATTCATTAAGAA[A/T]TGTAACACACAACTT | 51455 |
| rs781305250 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458979 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACGAGG | 51455 |
| rs781314363 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99422442 | AATCCACTTGGTAAT[A/G]TAGACTAGGAGGGCG | 51455 |
| rs781384385 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant | REV1 | GRCh38.p7 | 2:99412701 | AATATAAAGAGCAAC[A/G]GATGGCAAAATCTGT | 51455 |
| rs781399430 | in-del | -/CA | | | intron-variant | REV1 | GRCh38.p7 | 2:99468180 | AGCGAAACTCCATCT[-/CA]AAAAAAAAAAAAAGA | 51455 |
| rs781428956 | snp | C/G | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99438993 | AACTGCTGCAGAGTG[C/G]AGTCTCTGAAATCAG | 51455 |
| rs781470452 | snp | C/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99404635 | CTTGCTCTACTTGTT[C/G]CCGGAGATCAGGTGG | 51455 |
| rs781511503 | snp | C/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99418895 | TTTTAGGTGGTACTG[C/G]CCATCTGGTTTTGCT | 51455 |
| rs781578344 | in-del | -/AAT | | | intron-variant | REV1 | GRCh38.p7 | 2:99460668 | CTTAATTTTTCTAAA[-/AAT]AAAGTTATTTTACAG | 51455 |
| rs781581164 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99465000 | TCTGTATTGGGGAGG[-/A]AAAAAAAAATGTCAA | 51455 |
| rs781584237 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99452863 | ATAATGTATTAAGAG[A/G]ACAGACTCCAAAGCA | 51455 |
| rs781593266 | snp | A/G | 2.02677e-05 | 0.00318331 | intron-variant | REV1 | GRCh38.p7 | 2:99406109 | GCAGCCCGAAATACT[A/G]CAAAAAGAAAATATA | 51455 |
| rs781647286 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99473496 | TTAGCGACTGATTCT[A/C]AACCAAGCCAACAGT | 51455 |
| rs781728560 | snp | A/G | 1.67069e-05 | 0.00289019 | utr-variant-3-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99401217 | GGCACAGCTATCAGA[A/G]AGCATCAGGCTCTCT | 51455 |
| rs781734260 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99430939 | ATGAGTAAAACAAAC[C/T]CAAAATATATCACTT | 51455 |
| rs781734450 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99447276 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 51455 |
| rs781735799 | snp | A/G | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99410799 | ACGTTTACCCTTCAT[A/G]CCAGTGGCTTCTAGT | 51455 |
| rs781768646 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | REV1 | GRCh38.p7 | 2:99431850 | CACTGGAGGGCAAAG[C/T]AGAGAACTGCTCATC | 51455 |
| rs796148067 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99488010 | CATTCTACAAACGAG[-/A]AAAAAATCAGAGATA | 51455 |
| rs796148669 | in-del | -/AAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99486539 | ATCTCAAAAAAAAAA[-/AAAA]TTACCCTGTTCTAAG | 51455 |
| rs796178066 | in-del | -/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99489527 | CGGCGCGGGGCGGCC[-/C]ATGGGGCTGGCGGCG | 51455 |
| rs796192443 | in-del | -/AAAAAA | | | intron-variant | REV1 | GRCh38.p7 | 2:99454551 | GTGAAACTCCAGCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 51455 |
| rs796198556 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99428548 | TAAAATATAAGCATG[C/T]ACGTTTGAACTTAAT | 51455 |
| rs796215963 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99471798 | GGCCAATAAGCACAC[-/A]AAAAAAACGTTCAGT | 51455 |
| rs796242559 | in-del | -/AAAAAC | | | intron-variant | REV1 | GRCh38.p7 | 2:99454240 | AAAAAAAATCCACAA[-/AAAAAC]AAAAACAAAAACAAA | 51455 |
| rs796262338 | snp | A/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99454566 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 51455 |
| rs796268072 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99467876 | CATGGTGAAATCCCA[C/T]GTCTATTAAAAATAC | 51455 |
| rs796275383 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99418187 | AAACTTTCACTATAA[-/A]TGAAGATGGAAGACT | 51455 |
| rs796283766 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99457949 | AAATAAAAAAAAAAA[-/A]TTGTAAAACCTCAAA | 51455 |
| rs796329824 | in-del | -/TAATTG | | | intron-variant | REV1 | GRCh38.p7 | 2:99409246 | ATAAATTATGTTCTC[-/TAATTG]TAATTTATAATTCCT | 51455 |
| rs796333438 | multinucleotide-polymorphism | AA/CC | | | intron-variant | REV1 | GRCh38.p7 | 2:99454878 | AGTAAAAGTAAAAGC[AA/CC]TATACAAGGACCACA | 51455 |
| rs796337352 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99411597 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 51455 |
| rs796353288 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99486927 | AGTGGGAAAAAAAAA[-/A]CAGTGTATCTTCACC | 51455 |
| rs796381723 | in-del | A/CCC | | | intron-variant | REV1 | GRCh38.p7 | 2:99409865 | CAACCCCCCCCCCCC[A/CCC]AAAAAAACAGCGTTT | 51455 |
| rs796389879 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99471431 | AAAAAAAAACTTAAA[-/A]GTGTACAAAAGACAT | 51455 |
| rs796405124 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99455593 | TGGTAAGTCTTCTAT[A/G]TCAGAGGTTCAATTC | 51455 |
| rs796438420 | in-del | AAAAAAA/C | | | intron-variant | REV1 | GRCh38.p7 | 2:99454585 | AAAAAAAAAAAAAAA[AAAAAAA/C]CCAAAAATTACGTGT | 51455 |
| rs796472375 | snp | C/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99414629 | TGCTTTTAAGAAAGA[C/G]TTTTTTCTTCAATTT | 51455 |
| rs796485331 | multinucleotide-polymorphism | GG/TT | | | intron-variant | REV1 | GRCh38.p7 | 2:99419226 | TTTTTTTTTTTTTTT[GG/TT]GGGGATGGAGGCTCA | 51455 |
| rs796491610 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99468194 | TCAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAAAT | 51455 |
| rs796562518 | in-del | -/A | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99483868 | GACTCTTGGGGTCTC[-/A]CTTTCCTCCAGTAAG | 51455 |
| rs796586332 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99439971 | TGCACAAATAGACAA[A/G]AAGTAAAGCCATGTC | 51455 |
| rs796615833 | snp | G/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99437755 | AAGGCCAAGACATGA[G/T]GTAAGGATAATCTAG | 51455 |
| rs796651257 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99478527 | CTGATCTTCACTAAG[A/G]AGAAGTGGTATAATC | 51455 |
| rs796713195 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99458973 | CAGCACTTTGGGAGG[C/T]CAAGGTGGGCAGATC | 51455 |
| rs796749046 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99405560 | ACTGCAAAAACCCTT[C/T]GACATAAGGCCTCTA | 51455 |
| rs796799439 | snp | A/C | | | upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99490214 | TCCCCTCCCCGGCCC[A/C]GCCCTGTTGTTCTGC | 51455 |
| rs796817740 | snp | A/G | | | intron-variant | REV1 | GRCh38.p7 | 2:99422357 | GACTAAGAAATCACA[A/G]AATAGAACTGGACCA | 51455 |
| rs796844584 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | REV1 | GRCh38.p7 | 2:99480931 | CAATGTAACAATTTA[A/G]CACACTATAATCTCT | 51455 |
| rs796878108 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99469450 | CTCAAGTAATCAAAT[C/T]ATAAAGACCAACTGA | 51455 |
| rs796911125 | in-del | -/AAGTC | | | intron-variant | REV1 | GRCh38.p7 | 2:99465098 | AATGTCCAACTGATG[-/AAGTC]AAAGTATACAATATT | 51455 |
| rs796926771 | snp | C/T | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99482877 | CAAAACCCAGCTGGG[C/T]GTGGTGGCAGGTGCC | 51455 |
| rs796950192 | snp | A/G | | | intron-variant, upstream-variant-2KB | REV1 | GRCh38.p7 | 2:99484227 | TGAGTCTACTTAAGC[A/G]TGGAGGGTGGGAGGA | 51455 |
| rs796976106 | snp | C/T | | | intron-variant | REV1 | GRCh38.p7 | 2:99460233 | AGGCGCACGTCACCA[C/T]GCCCAGCTAATTTTT | 51455 |
| rs797014844 | in-del | -/A | | | intron-variant | REV1 | GRCh38.p7 | 2:99445143 | GAACAAAAAAAAAAA[-/A]CACAAGGAATGGCAA | 51455 |