SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs749213 | snp | A/T | 0.371582 | 0.218444 | intron-variant | TINCR | GRCh38.p7 | 19:5564229 | GACGGTACCCTAGGG[A/T]GAGAGAAGCTGCGTG | 257000 |
rs1806964 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TINCR | GRCh38.p7 | 19:5563732 | ccagcctggccaaca[A/T]ggtgaaacggtctct | 257000 |
rs2288946 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562073 | TTCTCAACTACTACA[A/G]TTACTTACCTGGAGT | 257000 |
rs2288947 | snp | A/G | 0.497641 | 0.0342639 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562104 | GAGATCTAGGCTCCC[A/G]GGAGGCAGGAGAAGT | 257000 |
rs7246801 | snp | C/T | 0.2768 | 0.248559 | intron-variant | TINCR | GRCh38.p7 | 19:5564522 | GTGTGTGGTCAGGGA[C/T]GGGCAAGGGGCAGGG | 257000 |
rs7249815 | snp | C/T | 0 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569907 | atggcacaatctcgg[C/T]tcaccgcaacctccg | 257000 |
rs7250122 | snp | C/T | 0.381503 | 0.21262 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559427 | GCAACCTCTGCCTCC[C/T]GGGTTCCCGCCATTC | 257000 |
rs8105637 | snp | A/G | 0.476487 | 0.105846 | intron-variant | TINCR | GRCh38.p7 | 19:5566221 | aaatgcagagacacc[A/G]gagagataaagagac | 257000 |
rs8113645 | snp | A/G | 0.377187 | 0.215229 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561065 | AAGGTGTGGCTGGGA[A/G]AATGTCCTGGGCAAG | 257000 |
rs10451477 | snp | C/G | 0.298398 | 0.245271 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560801 | CACAGTTGGAGGCCT[C/G]AGAAGGAGCTAGGAT | 257000 |
rs11085142 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557938 | CCCTGGCGGGGAGCG[A/G]GCAGGATTCCCTGAG | 257000 |
rs11670013 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TINCR | GRCh38.p7 | 19:5561893 | ACGGCTCTGGTCCAC[A/G]TGTTAGTCCAAAAAG | 257000 |
rs11880534 | snp | C/T | 0.243633 | 0.249919 | intron-variant | TINCR | GRCh38.p7 | 19:5563331 | ggcTGCGGACCTTGG[C/T]GGGGGGCAACTGGGC | 257000 |
rs12610531 | snp | A/G | 0.342582 | 0.232225 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559819 | AGGCTCTAGATACAC[A/G]CATGTGGCCCAGCTG | 257000 |
rs12610866 | snp | A/C/G | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5563520 | GGGAGAAGGTTTAGT[A/C/G]ATGAAGGGCGTGGCT | 257000 |
rs12980823 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5567627 | AGGGGTccccggccg[C/T]cgcccccgccccacc | 257000 |
rs12983488 | snp | C/T | 0.259397 | 0.249823 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559105 | GTGGTGATTTGCATG[C/T]GATTTGCATGTGATT | 257000 |
rs28594941 | snp | A/C | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568603 | GCCTGGAATCCCAGC[A/C]CTTTGGGAGACTGAG | 257000 |
rs28607963 | snp | A/C | 0.278399 | 0.248382 | intron-variant | TINCR | GRCh38.p7 | 19:5565073 | TCCCACCTCCCTCGG[A/C]GTCAAGGCCCAAGTC | 257000 |
rs34152404 | in-del | -/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559056 | ACATTATTATTTCAG[-/G]AACATGCCAGCGCTG | 257000 |
rs34278246 | in-del | -/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559151 | AATGTCAAAACACCC[-/C]TGAAAATGCTTTCTC | 257000 |
rs34526855 | in-del | -/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557804 | AGGTGGGCGGCCAAG[-/T]ACGGGAGGTGGCCCC | 257000 |
rs34657688 | in-del | -/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558786 | GCTGTGGGACCTTAG[-/G]CCCATGCCTCAGTTT | 257000 |
rs35571988 | in-del | -/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564237 | TTCTCTCTCCCTAGG[-/G]TACCGTCTGCGCTGA | 257000 |
rs35825675 | in-del | -/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559767 | GACGAGGCATGTCCC[-/C]TGAATATGCACAGGG | 257000 |
rs35974274 | in-del | -/T | 0.392696 | 0.205275 | intron-variant | TINCR | GRCh38.p7 | 19:5564515 | CAGCTGTGTGTGTGG[-/T]CAGGGATGGGCAAGG | 257000 |
rs45500293 | snp | C/T | 0.0119091 | 0.0762411 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560569 | CCGGAATTCCCACAA[C/T]GCACTCCCTGCAATG | 257000 |
rs45575840 | snp | C/G | 0.49703 | 0.0384237 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559889 | CTGCCTCCCCCTGCT[C/G]TGTGTCCCTGACAAC | 257000 |
rs56917160 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | TINCR | GRCh38.p7 | 19:5564894 | AAACTGTCTCCTCTG[A/C]AGGCTTCTGTTCTCT | 257000 |
rs58473504 | snp | A/G | 0.0310518 | 0.120672 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560783 | TTGGGGGTGGAAATG[A/G]GGCACAGTTGGAGGC | 257000 |
rs60466689 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | TINCR | GRCh38.p7 | 19:5567080 | AATGGAGAGAGAGAC[A/G]GAGACAAAGACAAAA | 257000 |
rs60513056 | in-del | -/AAGA | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569203 | AGAAAGAAAGAAAGA[-/AAGA]GGGAGAGAGAGAGAA | 257000 |
rs62637989 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TINCR | GRCh38.p7 | 19:5566367 | AGAGAAACAGAGAGA[C/T]AAAAGAGACACACAG | 257000 |
rs72977062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5563426 | GCTGAAGGACAGATA[A/G]AGGGGCTTGGGAGGA | 257000 |
rs73920015 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TINCR | GRCh38.p7 | 19:5561531 | GTGATCTGCAGTCAT[C/T]CCCTCCTGTGGATGT | 257000 |
rs73920016 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | TINCR | GRCh38.p7 | 19:5562298 | CTATTCTGCCCACTG[G/T]CTGGCTGGTGCCTCT | 257000 |
rs73920017 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TINCR | GRCh38.p7 | 19:5564305 | AGCTGAGGCCTCCCC[A/G]GCTGCTGCTGCACCA | 257000 |
rs74173058 | in-del | -/AAA | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568877 | AAAAAAAAAAAAAAA[-/AAA]TGGCCGGGTGTGGTG | 257000 |
rs74174330 | snp | C/T | 0.282105 | 0.24793 | intron-variant | TINCR | GRCh38.p7 | 19:5567590 | AGGCCGCCTTGGGCG[C/T]CCGCCTCCCCCGCCG | 257000 |
rs74411837 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558263 | CGGCCCCAAAGGTAG[C/T]GATGACTCTGCTGGG | 257000 |
rs74795022 | snp | G/T | 0.485187 | 0.0847778 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568593 | GGTGGCTCATGCCTG[G/T]AATCCCAGCACTTTG | 257000 |
rs74896816 | snp | A/G | 0.0349115 | 0.127424 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557888 | AACTCCTCATAGCCC[A/G]GACTTGCTCAGGGTG | 257000 |
rs75239626 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5565045 | CCCTCCTCTGCCCAC[A/C]GCCCTCTATGGCTCC | 257000 |
rs76001042 | snp | C/G/T | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569831 | TTACACAAACATCAC[C/G/T]TTTTTTTTTTTTTTT | 257000 |
rs77608060 | snp | A/C | 0.00119737 | 0.0244387 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5567764 | TTGTAGTAGAAGGCG[A/C]GCTTCCAGGAGCTCA | 257000 |
rs78647018 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | TINCR | GRCh38.p7 | 19:5562430 | CCTCTGCTCACGATT[A/G]TGTTAGTGAGACAAT | 257000 |
rs79094586 | snp | G/T | 0.0146672 | 0.084371 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561370 | AGCTGGTCAGGCCAG[G/T]GTTTCATGGTCCACC | 257000 |
rs79327432 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565738 | CCAGACTCCTGCAAC[A/C/G]GGGTGGCATCTGAGG | 257000 |
rs79820213 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569849 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTTT | 257000 |
rs111235842 | snp | A/G | 0.5 | 0 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560907 | ACAAAGGGCCTGTGG[A/G]GGCCCCAAAGAAGGC | 257000 |
rs111322013 | snp | G/T | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5564514 | CCAGCTGTGTGTGTG[G/T]TCAGGGATGGGCAAG | 257000 |
rs111526643 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569185 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 257000 |
rs111573120 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566820 | GACACACACACAGAG[A/G]AAAAAAGCAGAGACC | 257000 |
rs111780351 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5564273 | CCCAAGTGTTTTTCT[C/T]ATTTCTCACATGGGG | 257000 |
rs112021269 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565034 | TCAGGTCCCGTCCCT[C/T]CTCTGCCCACAGCCC | 257000 |
rs112098968 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TINCR | GRCh38.p7 | 19:5563802 | CGCCTGTAATCCCAG[C/T]TACTCAGGAGACTGA | 257000 |
rs112164487 | snp | G/T | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5564515 | CAGCTGTGTGTGTGG[G/T]CAGGGATGGGCAAGG | 257000 |
rs112451690 | snp | A/G | 0.5 | 0 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559106 | TGGTGATTTGCATGC[A/G]ATTTGCATGTGATTT | 257000 |
rs114008877 | snp | A/G | 0.0379877 | 0.132479 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559635 | CCACCGCGCCTGGCC[A/G]GCTGTCAATCAAGTG | 257000 |
rs115018845 | snp | A/T | 0.0185938 | 0.0946107 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559653 | TGTCAATCAAGTGAG[A/T]CAGGGCTCCAAAAAG | 257000 |
rs115757604 | snp | A/G | 0.0150606 | 0.0854603 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559226 | CCTCCACCAGCTCCC[A/G]GCATGGGTTGGGGAC | 257000 |
rs115816841 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562115 | TCCCGGGAGGCAGGA[G/T]AAGTGCCTTCCAAAA | 257000 |
rs117012071 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TINCR | GRCh38.p7 | 19:5564196 | AGAGAGGGCCTGGCA[C/G]GTTTGTCCCGAGCAG | 257000 |
rs117030331 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TINCR | GRCh38.p7 | 19:5565594 | AGAAGGTACGCTGCC[A/G]AGAACACCCTCTCCT | 257000 |
rs117305966 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TINCR | GRCh38.p7 | 19:5565516 | GGCACACAATAAATG[C/T]TGACTCTGTACTGCA | 257000 |
rs117655447 | snp | A/G | 0.0217236 | 0.101931 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557998 | GCCTGGGGTCAACTG[A/G]AGTAACAGTGTCACC | 257000 |
rs137918324 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559358 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 257000 |
rs137971419 | in-del | -/AGAG | 0.0479149 | 0.147179 | intron-variant | TINCR | GRCh38.p7 | 19:5567095 | AGAGACAAAGACAAA[-/AGAG]AGAGAGGTGAGGAGA | 257000 |
rs138458164 | snp | C/T | 0.00119737 | 0.0244387 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559909 | TCCCTGACAACCTCC[C/T]TGGGCCTCAGGCTAC | 257000 |
rs138492500 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TINCR | GRCh38.p7 | 19:5565445 | TGAAGGCGAAATCTG[G/T]TCTCTCTGGGTCACT | 257000 |
rs138533582 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | TINCR | GRCh38.p7 | 19:5564450 | ACAGCAAAGGCAGAT[-/A]GGGGCCCCTGTCTGT | 257000 |
rs138897422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567059 | AGAGGAAAAAACAGA[G/T]ACCAAAATGGAGAGA | 257000 |
rs139157509 | snp | C/T | 0.0341408 | 0.126114 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568844 | ACAGAGCGAGACTTA[C/T]CGCAAAAAAAAAAAA | 257000 |
rs139265480 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TINCR | GRCh38.p7 | 19:5562629 | GGGAAAGAGAGAAAG[C/T]AGGGATGGCGTGAAA | 257000 |
rs139853105 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569743 | TTTCCCAGAGGAAAC[A/C]GAGAGAAAAGTGGCA | 257000 |
rs139980198 | in-del | -/TT | 0.384401 | 0.210799 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559335 | GTGAGGCTGTCAATC[-/TT]TTTTTTTTTTTTTTT | 257000 |
rs140195060 | snp | A/G | 0.00318978 | 0.0398085 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558634 | GTTCCCCTTGGCCCT[A/G]TCAAGCCTATCAGGC | 257000 |
rs141422868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566380 | GACAAAAGAGACACA[C/G]AGAGAGAAAAAGAGC | 257000 |
rs142186312 | snp | A/G | 0.0138799 | 0.0821421 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558250 | CTGGGTGATCCTGCG[A/G]CCCCAAAGGTAGTGA | 257000 |
rs142563466 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TINCR | GRCh38.p7 | 19:5564760 | TGTTTGTATTTTTAG[C/T]AGAGACAGCGTTTCG | 257000 |
rs142848587 | in-del | -/AGAC | 0.00716266 | 0.059414 | intron-variant | TINCR | GRCh38.p7 | 19:5566636 | GACAAATGGACAAAG[-/AGAC]AGAGAGACAGGGAGA | 257000 |
rs142989275 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560073 | GGCACACCCAGGGGC[C/T]AGCAAGACCCAAGTC | 257000 |
rs143214372 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569913 | CAATCTCGGCTCACC[A/G]CAACCTCCGCCTCCC | 257000 |
rs144530222 | snp | A/C | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568817 | TTGTGCCACTGCACT[A/C]CAGCCTGAGCCACAG | 257000 |
rs144595015 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TINCR | GRCh38.p7 | 19:5565014 | GGTTGCCTGTGAGCA[C/T]TGAGTCAGGTCCCGT | 257000 |
rs144964531 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569332 | AATCCCAACACTTTG[A/G]GAGGCCGAGGTGGGC | 257000 |
rs144974663 | in-del | -/A | | | intron-variant | TINCR | GRCh38.p7 | 19:5562246 | AGACACAGGTTGCAG[-/A]AAAAACATAGCCCTT | 257000 |
rs145298912 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557923 | CCAGAGTCTGAGAGG[C/T]CCTGGCGGGGAGCGA | 257000 |
rs145448639 | in-del | -/AG | 0.0260105 | 0.111035 | intron-variant | TINCR | GRCh38.p7 | 19:5566596 | GAGACACAGAGAGAC[-/AG]AGAGAGAAAAACAGC | 257000 |
rs145561914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564242 | TCTCCCTAGGGTACC[A/G]TCTGCGCTGACAGGT | 257000 |
rs145905786 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559802 | GAGGACAGAGGGGAC[C/T]CAGGCTCTAGATACA | 257000 |
rs146114884 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561240 | AACCTCAAAGTCACA[C/T]AGCAGAGCTGAAAGG | 257000 |
rs147245240 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568604 | CCTGGAATCCCAGCA[C/T]TTTGGGAGACTGAGG | 257000 |
rs147633982 | snp | A/G | 0.0123036 | 0.0774623 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5558026 | ACCTGGAGTAACAGC[A/G]TCACCTGGAGTAACA | 257000 |
rs148109864 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568138 | GCCCCAGAGTGCGCC[C/T]GGGGGTCTAGAGGCG | 257000 |
rs148336825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561620 | TTTCTTTCTTTTTTT[C/T]GAGACAGAGTCCTGC | 257000 |
rs148492276 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557833 | CCTCCCCAGAACGCC[A/G]CGGGCCTTAGCGAGA | 257000 |
rs148951692 | in-del | -/A | 0.031825 | 0.122064 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559124 | TTGCATGTGATTTGC[-/A]TACTGTTTGTTAAAT | 257000 |
rs149921261 | snp | C/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569261 | AGAAAGAAAGAGAGA[C/G]AGAGAGGAAGAGAAG | 257000 |
rs150255652 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5566943 | AGTGGGCAGAGACAC[A/T]GAGTGACAGAGAAAA | 257000 |