SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9288 | snp | A/G | 1.72982e-05 | 0.00294088 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113815 | GTAAAGGCGCATGGC[A/G]TCCTCGGCCCGCGCA | 1155 |
rs1046975 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121555 | TTTCCTGAAGCGCAG[A/C]AAGCTCGGCCGGTAC | 1155 |
rs1048259 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114755 | GAAGGCGGGCGAGGA[A/G]TGGCTCCAGGACTAA | 1155 |
rs1801989 | snp | C/T | 0.000375607 | 0.013699 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125751 | CGGTGGGGGACTTCC[C/T]GGAGGAGGACTACGG | 1155 |
rs1801990 | snp | A/C | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125502 | TCCGCTATGATGAGC[A/C]ACTGGGGAAAAATGA | 1155 |
rs1803271 | snp | A/T | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121707 | CTCGCCGGGGCACCG[A/T]CATGTATGTAGGTCT | 1155 |
rs1803272 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125795 | TGACACCTAAGGAAT[G/T]CCCCTGCTTCAGCTC | 1155 |
rs2072606 | snp | C/T | 0.4628 | 0.13121 | intron-variant | TBCB | GRCh38.p7 | 19:36121324 | GTGCAGGCGGCACCC[C/T]TTCCATTTACGATTG | 1155 |
rs2075474 | snp | A/G | 0.477098 | 0.104529 | intron-variant | TBCB | GRCh38.p7 | 19:36121494 | TTAGGCCCGGCCGAC[A/G]CCCCAACTGACCCCA | 1155 |
rs2227260 | snp | C/T | 0.452595 | 0.146476 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114745 | GTGCCAGGGGTTAGT[C/T]CTGGAGCCATTCCTC | 1155 |
rs2230684 | snp | C/T | 0.000611101 | 0.0174693 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114227 | CCAGATTATCGCCGA[C/T]GTGTCCCAGGACCCC | 1155 |
rs2231566 | snp | A/G | 0.143717 | 0.226283 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114650 | GCCGGGGAAGACCCC[A/G]GCGCTCACCGCGTAG | 1155 |
rs2231567 | snp | C/T | 0.0114531 | 0.0748023 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114680 | GAGCAGAATGCGGTT[C/T]TCCTTGTCTTCCTTG | 1155 |
rs2231568 | snp | C/T | 0.455003 | 0.143087 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114892 | GCCCTCCCAGCCTTC[C/T]GCGCTTGCTCCGCCG | 1155 |
rs2231569 | snp | G/T | 0.0490535 | 0.14873 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114973 | CGGAGCTGCGCACAC[G/T]TGCTGGCTCCCCGCC | 1155 |
rs2231570 | snp | C/T | 0.0543475 | 0.155628 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115182 | GGACAGAAGCCAAGG[C/T]GCTTGGCTTGGTTGA | 1155 |
rs2231571 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115242 | TCGCGGACTGGGCGA[A/G]CTCTTGCCACTCCTA | 1155 |
rs2231572 | snp | C/G | 0.0150606 | 0.0854603 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115386 | AGAGCCCTCTTCCTG[C/G]CGGTGGGGAAGGGAC | 1155 |
rs2231573 | snp | C/T | 0.00191612 | 0.0308932 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120727 | CATTGACCACAGTGG[C/T]GCCCGCCTTGGTGAG | 1155 |
rs2231574 | snp | G/T | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36120833 | TGGGCGTCGAGGGGT[G/T]CGTGGGGGCCAGAGG | 1155 |
rs2231575 | snp | A/G | 0.00759075 | 0.0611372 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121579 | CCGGTACAACGAGGA[A/G]GAGCGGGCTCAGCAG | 1155 |
rs2231576 | snp | A/G | 0.0152535 | 0.0859889 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121744 | CGCGGGCCCGGTCCC[A/G]GGCTCCAGGGCTCCA | 1155 |
rs2231577 | snp | A/G | 0.0038934 | 0.0439493 | intron-variant | TBCB | GRCh38.p7 | 19:36125654 | ACCACACCCACCCCT[A/G]TCCTTTCCTGCAGTG | 1155 |
rs2239509 | snp | C/T | 0.114387 | 0.210022 | intron-variant | TBCB | GRCh38.p7 | 19:36120359 | CAGCTTAGGAGAGTC[C/T]CAGAGGCCCATCGAG | 1155 |
rs2239510 | snp | A/G | 0.383824 | 0.211166 | intron-variant | TBCB | GRCh38.p7 | 19:36120382 | CCATCGAGGAGATGC[A/G]CTGTGCACAGGGCTG | 1155 |
rs4555271 | snp | A/G | 0.337841 | 0.23406 | intron-variant | TBCB | GRCh38.p7 | 19:36119288 | ACGCTTCATCCGGAG[A/G]TAAAGGCCATTCCTA | 1155 |
rs4806277 | snp | C/T | 0.279726 | 0.248226 | intron-variant | TBCB | GRCh38.p7 | 19:36124646 | cctcccgggttcaaa[C/T]ggttctcctgcctca | 1155 |
rs6510521 | snp | G/T | 0.497855 | 0.0326773 | intron-variant | TBCB | GRCh38.p7 | 19:36124781 | atctcctgacctcgt[G/T]atccaccctcctcag | 1155 |
rs7258441 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115456 | TTGGTCAGGCACGGA[G/T]CAGGAGGCGGGGCTG | 1155 |
rs8100250 | snp | A/G | 0.466824 | 0.124448 | intron-variant | TBCB | GRCh38.p7 | 19:36124851 | cccggccAgtatgtc[A/G]tcttttgagaagtgt | 1155 |
rs8103791 | snp | C/T | 0.201727 | 0.245295 | intron-variant | TBCB | GRCh38.p7 | 19:36119890 | gacagagcgagactc[C/T]gtcaaaaaaaaaaaa | 1155 |
rs8104047 | snp | A/G | 0.482757 | 0.0912364 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122012 | GGCAGTGTCAGTCGC[A/G]GTGGGGAAACGGGCG | 1155 |
rs8104053 | snp | A/G | 0.477175 | 0.104362 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122023 | TCGCGGTGGGGAAAC[A/G]GGCGGCGTGACCAAG | 1155 |
rs8106074 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126088 | TGTAGCTACCAGGAA[A/G]AAAGGGAAGGGAAGG | 1155 |
rs8106396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117234 | atttactctctgtct[C/T]cctggattcgagtgc | 1155 |
rs8110206 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36125987 | GACCCACTGGGTAAA[C/T]AGTGGCCCTTCGGTA | 1155 |
rs8113579 | snp | A/G | 0.202651 | 0.245475 | intron-variant | TBCB | GRCh38.p7 | 19:36119361 | GTGTTCCTTGGGCCC[A/G]CTCTCTCCCTCACCC | 1155 |
rs10407011 | snp | A/G | 0.383824 | 0.211166 | intron-variant | TBCB | GRCh38.p7 | 19:36119883 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCAAAAA | 1155 |
rs10410489 | snp | C/T | 0.029116 | 0.117091 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121963 | GGAGGAAGCAGAAGC[C/T]AGAGGCACGCGGCCT | 1155 |
rs10410926 | snp | A/G | 0.279726 | 0.248226 | intron-variant | TBCB | GRCh38.p7 | 19:36122874 | caaattgtgaacatc[A/G]tacccaacagataat | 1155 |
rs10417569 | snp | A/G | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36123535 | ctcccaaagtgctgg[A/G]attacaggtgtgagc | 1155 |
rs10417577 | snp | A/G | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36123545 | gctgggattacaggt[A/G]tgagccaccatgcta | 1155 |
rs10418079 | snp | C/G | 0.398714 | 0.200958 | intron-variant | TBCB | GRCh38.p7 | 19:36123073 | cttttgtaactggcg[C/G]cttccactgagcaga | 1155 |
rs10419924 | snp | A/C | 0.339203 | 0.233544 | intron-variant | TBCB | GRCh38.p7 | 19:36123560 | gtgagccaccatgct[A/C]ggcctgaacattctt | 1155 |
rs10420582 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TBCB | GRCh38.p7 | 19:36118254 | TGTTGGCTAAATGGC[C/T]AGAGGACTGAATGTG | 1155 |
rs10425477 | snp | C/T | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36123544 | tgctgggattacagg[C/T]gtgagccaccatgct | 1155 |
rs10425700 | snp | A/G | 0.338069 | 0.233974 | intron-variant | TBCB | GRCh38.p7 | 19:36118888 | GTGTGTGGGGAACAG[A/G]TGGTGGAGGACAGGA | 1155 |
rs11267762 | in-del | -/TCATGGCCAACATG | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116829 | TTTGCCATGTTGGCC[-/TCATGGCCAACATG]AGGCTGGTCTGGAAC | 1155 |
rs11310846 | in-del | -/T | 0.125874 | 0.217008 | intron-variant | TBCB | GRCh38.p7 | 19:36121200 | GGACGGATCGAGTGT[-/T]GGGGGAGACCGGGGG | 1155 |
rs11540331 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115145 | CGATGCGCATCGTAA[A/C]CCGCAAAACACTGAG | 1155 |
rs11545600 | snp | A/C/T | 6.22452e-05 | 0.00557842 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115545 | CGCGCTGCAGGCATC[A/C/T]GCAGGGCGCGGCAAG | 1155 |
rs11545601 | snp | A/G | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121623 | CCCAGCGCCTGGCCG[A/G]GGAGAAGGCCCAGGC | 1155 |
rs12971639 | snp | C/T | 0.472241 | 0.114494 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126204 | AGGGCGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 1155 |
rs12971936 | snp | C/T | 0.472241 | 0.114494 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126338 | GAGGCAGGAGAATGG[C/T]GAGAACCTGGGAGGC | 1155 |
rs12972828 | snp | A/G | 0.449979 | 0.150028 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126371 | AGCTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 1155 |
rs12981995 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36122666 | aggctgaggtgggag[A/G]atggcttgagcccgg | 1155 |
rs34390728 | in-del | -/A | 0.0954561 | 0.19651 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113834 | TGGCAGAAATGATGC[-/A]TGGTTAGGAAGGATT | 1155 |
rs34683365 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116835 | ATGTTGGCCAGGCTG[-/AG]GTCTGGAACTCCTGA | 1155 |
rs34701186 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117236 | TACTCTCTGTCTCCC[-/C]TGGATTCGAGTGCCC | 1155 |
rs35581971 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121651 | GCCAGCTCCATCCCC[-/C]GTGGGCAGCCGCTGT | 1155 |
rs35625281 | in-del | -/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36119949 | TGTCTTCCACTCTCC[-/C]TCTGGCTCGCTCCAC | 1155 |
rs35947741 | in-del | -/A | | | intron-variant | TBCB | GRCh38.p7 | 19:36122590 | AAAAAAAAAAAAAAA[-/A]TCCCACAAAACTTTT | 1155 |
rs36073528 | in-del | -/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36119387 | ACCCCCACATCCACT[-/G]CTCATCAAATCCTCT | 1155 |
rs45471297 | snp | C/G | 0.0119091 | 0.0762411 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115262 | TGCCACTCCTACCTC[C/G]GGGCTTCAGTCTTCG | 1155 |
rs55911548 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36120568 | CTCCCTTCCGCTGGG[A/C]TCAGGAGAGAAGAGA | 1155 |
rs57123860 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123274 | TTTTTTTTTTTTTTT[-/T]CTAATTTGAGACAGC | 1155 |
rs57766416 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124993 | TTCTGCTCAGTTTTT[-/T]CATTGGGATGCTGTC | 1155 |
rs58457494 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116052 | ACAGTGTAAACTGGA[A/G]TTGCTGGTGGGCAGC | 1155 |
rs60393405 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | TBCB | GRCh38.p7 | 19:36118165 | TCTCGTTGATTAACT[C/G]TTCATTCCCCATCTG | 1155 |
rs60910092 | in-del | -/G | 0.0678174 | 0.1712 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126174 | ACGCCTGTAATCCCA[-/G]CACTTTGGGAGGCCA | 1155 |
rs61736267 | snp | A/C | 0.020313 | 0.0987111 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113458 | ATCTGTGCAGGGATC[A/C]GGCCCTTCCGCTGCA | 1155 |
rs62111380 | snp | C/T | 0.118933 | 0.212888 | intron-variant | TBCB | GRCh38.p7 | 19:36117504 | TGTGCACCACCACGC[C/T]TGGCTAATTTTGTAA | 1155 |
rs62111381 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | TBCB | GRCh38.p7 | 19:36118350 | CTGATGCATCAGTGA[C/T]GTCTGGGAGGACATC | 1155 |
rs62111382 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36119912 | AAAAAAAAAAAAACC[A/C]AAAGTCTCCAGCAGT | 1155 |
rs73036138 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113076 | TGTATGTGGGGTATG[A/G]AGAATCAAGACATGA | 1155 |
rs73601689 | snp | A/G | 0.0626037 | 0.165477 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122173 | GGAGTAGCGGGTGCA[A/G]GTGAGCAGAGCGCAG | 1155 |
rs73601695 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | TBCB | GRCh38.p7 | 19:36124370 | GGATTATAGGTGAGC[A/G]CTACAACACCTGGCT | 1155 |
rs74172781 | in-del | -/G | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36118714 | AGGTTAACTGAAGAT[-/G]GGGGAAGGGGTGCCC | 1155 |
rs74572952 | snp | A/C | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36122757 | AGACCCTGTCTCCAA[A/C]AAAAAAAAAAAAAAA | 1155 |
rs74892215 | in-del | -/AAAAA | | | intron-variant | TBCB | GRCh38.p7 | 19:36118696 | AAAAAAAAAAAAAAA[-/AAAAA]GGTTAACTGAAGATG | 1155 |
rs74928101 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116495 | AAGGGTGACTTAAGA[A/G]AAAGAGGTGGAAAGG | 1155 |
rs75130259 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TBCB | GRCh38.p7 | 19:36119991 | CACCCACTCTAGAGC[A/G]TGAAGGACATTTCTA | 1155 |
rs75674576 | snp | A/G | 0.000175731 | 0.00937203 | intron-variant | TBCB | GRCh38.p7 | 19:36121491 | CTGTTAGGCCCGGCC[A/G]ACACCCCAACTGACC | 1155 |
rs75735458 | snp | A/G | 0.0325976 | 0.123435 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117192 | TAATTCTCCTCTGAC[A/G]CACTCTGGATTTCTC | 1155 |
rs75814442 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116392 | AATCCCAGGGGACTG[A/G]AGCCACCAAGAAGAG | 1155 |
rs76039766 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | TBCB | GRCh38.p7 | 19:36123108 | TTTCAAGTTTCATCC[A/G]TGGCATGCCTGTGTC | 1155 |
rs76334680 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TBCB | GRCh38.p7 | 19:36118776 | AAGGTGGGAGGGAGC[A/G]CGGTGGGGATTAAGA | 1155 |
rs76448723 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116255 | ACAGACACTTGCTGG[A/G]CTTTGCCCTCAGTCA | 1155 |
rs76559835 | snp | C/G | 0.109108 | 0.206518 | intron-variant | TBCB | GRCh38.p7 | 19:36122979 | CCATCCCCCAGTCGT[C/G]TTCAGCCACTAATTT | 1155 |
rs76615582 | in-del | -/CC | | | intron-variant | TBCB | GRCh38.p7 | 19:36122753 | AGGGAGACCCTGTCT[-/CC]AAAAAAAAAAAAAAA | 1155 |
rs76953459 | snp | C/G | 0.0130508 | 0.0797186 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114007 | TAGAAAGCCCTCGCG[C/G]CACTTACCTCGGCCC | 1155 |
rs77095979 | snp | A/C | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36122759 | ACCCTGTCTCCAAAA[A/C]AAAAAAAAAAAAAAG | 1155 |
rs77581492 | in-del | -/AGC | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115490 | CCCAGCAGCAGCAGC[-/AGC]GGCGGCGGCGGCTGC | 1155 |
rs78029023 | snp | A/G | 0.111224 | 0.207945 | intron-variant | TBCB | GRCh38.p7 | 19:36123448 | TGTGGTTTTTTTTGT[A/G]GGATGGGATTTCGCC | 1155 |
rs78464082 | in-del | -/CAACA | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116833 | CCATGTTGGCCAGGC[-/CAACA]TGGTCTGGAACTCCT | 1155 |
rs78689013 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TBCB | GRCh38.p7 | 19:36120085 | TTTTGGGAAGCCTAC[C/T]CTCCCATGCTCCTTA | 1155 |
rs78849072 | snp | A/G | 0.108048 | 0.20579 | intron-variant | TBCB | GRCh38.p7 | 19:36122209 | CCACCTGGGGAAGGG[A/G]AGCGGGAGGAGAGGG | 1155 |
rs78885567 | snp | A/G | 0.105569 | 0.204058 | intron-variant | TBCB | GRCh38.p7 | 19:36124976 | TTCTTTGAGTTCCTT[A/G]TATATTCTTCTGCTC | 1155 |
rs79608574 | snp | C/T | 0.0952156 | 0.196321 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121992 | CTGTGCGCTTCGAAG[C/T]GTGGGGCAGTGTCAG | 1155 |
rs79645164 | snp | A/G | 0.109108 | 0.206518 | intron-variant | TBCB | GRCh38.p7 | 19:36125228 | TTCACCCAGTGAATG[A/G]GGGACAGGGGTGGAA | 1155 |