SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs951058 | snp | C/T | 0.494733 | 0.0510469 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401154 | TGTATTCTTAAACCT[C/T]AAAAAATACAGAATT | 81550 |
rs952805 | snp | A/G | 0.24932 | 0.249999 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405371 | TACATATTCAAACAT[A/G]CTGCATCTATAAAGA | 81550 |
rs1033854 | snp | A/G | 0.463666 | 0.129795 | downstream-variant-500B | TDRD3 | GRCh38.p7 | 13:60573986 | TATTCTGTAATTGTA[A/G]GGGGAGGCTTCAGTA | 81550 |
rs1341840 | snp | A/G | 0.464203 | 0.128908 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411058 | TGTTGTTAGTGCAAA[A/G]TGGCCACCCAAAATA | 81550 |
rs1341841 | snp | A/G | 0.24932 | 0.249999 | intron-variant | TDRD3 | GRCh38.p7 | 13:60411174 | AAGACTTAGTTAGCT[A/G]TGATAGTTCACAATT | 81550 |
rs1341842 | snp | A/G | 0.564238 | 0.17936 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414318 | GCTACCAGTTTTTGT[A/G]AATAACATTTTAGTA | 81550 |
rs1390155 | snp | A/C | 0.42666 | 0.176893 | intron-variant | TDRD3 | GRCh38.p7 | 13:60481351 | TACAAAAAAAAAAAA[A/C]ACACAAAGAGGGAAG | 81550 |
rs1418059 | snp | C/G | 0.486332 | 0.08153 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405290 | AATAATTCTTAAACA[C/G]CATATTGTGGCAGGC | 81550 |
rs1495275 | snp | A/G | 0.216048 | 0.247684 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397912 | AAGGGGTAAGAAGAG[A/G]CGGCTCCGGCCGCAG | 81550 |
rs1495276 | snp | C/T | 0.486855 | 0.0799975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60397787 | GCCTCCCGATCCCGC[C/T]GCAGAAACACCCCCT | 81550 |
rs1603204 | snp | C/G | 0.212122 | 0.247114 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488046 | GAGACACCCAGTCTA[C/G]ATCCTGCTGCTCACT | 81550 |
rs1603205 | snp | A/C | 0.482831 | 0.0910472 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488252 | ggtaaggaagcaatt[A/C]tgatgaatgaggggt | 81550 |
rs1845644 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | TDRD3 | GRCh38.p7 | 13:60474353 | GTCACTACCGGTCTC[C/T]GCGCCTTGGTGGTAG | 81550 |
rs1994971 | snp | A/C | 0.2462 | 0.249971 | intron-variant | TDRD3 | GRCh38.p7 | 13:60485100 | TGGTGTCAATATGAT[A/C]TGTTTATATTACTGA | 81550 |
rs2009015 | snp | A/G | 0.254944 | 0.249951 | intron-variant | TDRD3 | GRCh38.p7 | 13:60405019 | agatggcaaagaggg[A/G]caagccacatcttat | 81550 |
rs2038629 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TDRD3 | GRCh38.p7 | 13:60549857 | ATCGTATTTTTTTTC[A/G]TGACAAAGTGTTGTC | 81550 |
rs2047224 | snp | A/T | 0.479258 | 0.0997024 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427447 | atggagctgctgcat[A/T]agaaacgaaactgca | 81550 |
rs2047225 | snp | A/T | 0.246485 | 0.249975 | intron-variant | TDRD3 | GRCh38.p7 | 13:60486304 | TTTTTTGGGGATAAT[A/T]TCCCCTTATTAATAG | 81550 |
rs2077961 | snp | A/C | 0.482534 | 0.0918038 | intron-variant | TDRD3 | GRCh38.p7 | 13:60559451 | CTATTTAATCTTTAG[A/C]AATGGGTTTCAGAGA | 81550 |
rs2146356 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496014 | gagattaacatttga[A/G]tcagtgacttgggaa | 81550 |
rs2181294 | snp | A/G | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60546077 | ATCATTTAAAGTTTA[A/G]AAAGCCTCTAAAAGC | 81550 |
rs2181295 | snp | A/G | 0.4661 | 0.125701 | intron-variant | TDRD3 | GRCh38.p7 | 13:60568115 | CCTAGAATGTGATAT[A/G]TCTTTATCTTCCCCA | 81550 |
rs2181296 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TDRD3 | GRCh38.p7 | 13:60537997 | ATCATGCTTTCTATT[C/T]AATGATTTATGCTTA | 81550 |
rs2181297 | snp | A/C | 0.444444 | 0.157135 | intron-variant | TDRD3 | GRCh38.p7 | 13:60496343 | tatatatatatatat[A/C]tcctctaaagttttg | 81550 |
rs2273885 | snp | C/T | 0.228253 | 0.249052 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565588 | TCTCAGCAAATACAG[C/T]GTCCTATCTCTGTGT | 81550 |
rs2322909 | snp | C/T | 0.194278 | 0.243711 | intron-variant | TDRD3 | GRCh38.p7 | 13:60440922 | AATGTATAAATCTAA[C/T]GTTAAAAAAGTTACT | 81550 |
rs3081884 | in-del | -/CTTT | 0.24932 | 0.249999 | intron-variant | TDRD3 | GRCh38.p7 | 13:60422755 | TCTCTGACATTTCTT[-/CTTT]ATTTAAATTCTCATA | 81550 |
rs3081885 | in-del | -/GTT | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60427358 | GATTTTTGTTCTGTT[-/GTT]TTACACTGATGAATA | 81550 |
rs3081887 | in-del | -/GTT/TTG | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60437016 | TTTTGTCTGTGTGAG[-/GTT/TTG]CTGAAGTATCTAGCT | 81550 |
rs3081890 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438961 | GTTGAGTTTATCAAA[-/AA]GAGTTTCAAAATGTC | 81550 |
rs3813902 | snp | C/T | 0.495174 | 0.0488838 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396407 | CGCCCAATCGCGCGG[C/T]AGCGTCCGCCGTGCC | 81550 |
rs3832887 | in-del | -/T | 0.466412 | 0.125164 | intron-variant | TDRD3 | GRCh38.p7 | 13:60572820 | GTTGAAATTTTTTTT[-/T]GACAATCTGGTCCAG | 81550 |
rs3841371 | in-del | -/TACTACTGCA | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395855 | GACTTAAACACTGCA[-/TACTACTGCA]CATTGCAGCGAACAG | 81550 |
rs4054854 | in-del | -/GTA | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60445913 | CATAGAATAGTAGTA[-/GTA]NNCAGAGATTCTTGT | 81550 |
rs4243017 | snp | C/T | 0.361684 | 0.223667 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564303 | TATACTTTAGGGAGA[C/T]GTGAGACTTCAATCA | 81550 |
rs4259933 | snp | C/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500204 | aagtcaccatgcaac[C/T]tgaactgcctatcat | 81550 |
rs4297583 | snp | A/G | 0.363776 | 0.222609 | intron-variant | TDRD3 | GRCh38.p7 | 13:60564352 | ATTGGTTTGGTCAAG[A/G]CGGGACAACTTGAAG | 81550 |
rs4441150 | snp | C/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60500529 | gtggacagctacagc[C/T]tacagcccctttcta | 81550 |
rs4886223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399013 | GCTTTCCAACATGAC[C/T]CCCCCTCCTTTGGAA | 81550 |
rs4886224 | snp | C/G | 0.249886 | 0.25 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399016 | TTCCAACATGACCCC[C/G]CCTCCTTTGGAAAGA | 81550 |
rs4886225 | snp | G/T | 0.268452 | 0.249318 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416092 | GGCTCAAAAATTGTG[G/T]TTTGGAAGTTGATAA | 81550 |
rs4886226 | snp | G/T | 0.287085 | 0.247234 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416226 | GTAAAGTGTAAAGAT[G/T]TTTAGAGGAAGATGT | 81550 |
rs4886227 | snp | A/G | 0.286825 | 0.247273 | intron-variant | TDRD3 | GRCh38.p7 | 13:60416372 | GCTCTTACCTTTCCC[A/G]TGATCAGTTGAGCTG | 81550 |
rs4886229 | snp | C/T | 0.492775 | 0.059668 | intron-variant | TDRD3 | GRCh38.p7 | 13:60429729 | CTAGAAATATGTAGT[C/T]AGGCTTACCAGTAAG | 81550 |
rs4886230 | snp | A/G | 0.24932 | 0.249999 | intron-variant | TDRD3 | GRCh38.p7 | 13:60444429 | GAGAAGAGTTAGTAA[A/G]TAAAAAGGTTACCTA | 81550 |
rs4886231 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | TDRD3 | GRCh38.p7 | 13:60450975 | TACACACACAGATCA[C/T]GCATACACACACACT | 81550 |
rs4886234 | snp | C/G | 0.397452 | 0.201886 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488620 | gctctgttgcccagg[C/G]tggagtgcagtggcg | 81550 |
rs4886235 | snp | A/G | 0.48692 | 0.0798058 | intron-variant | TDRD3 | GRCh38.p7 | 13:60501472 | CCTTTTGGGATAAGT[A/G]GCATTGGATTTGGAT | 81550 |
rs4886236 | snp | A/G | 0.489434 | 0.0719116 | intron-variant | TDRD3 | GRCh38.p7 | 13:60511716 | CTTACAGGCTCACCC[A/G]TTCTAGCAGAATTCA | 81550 |
rs4886237 | snp | G/T | 0.483636 | 0.0889627 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539225 | TAGTACATCTCTTAG[G/T]TGTCGGGCACTGTTC | 81550 |
rs4886238 | snp | A/G | 0.379942 | 0.213577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60539605 | TATTTTCATGTTAGC[A/G]TACTTTAAAATGAAG | 81550 |
rs4886239 | snp | A/G | 0.487558 | 0.0778863 | intron-variant | TDRD3 | GRCh38.p7 | 13:60545328 | AATATAGACTTTTCA[A/G]AAACTTCTATTTAAC | 81550 |
rs5804002 | in-del | -/C | | | intron-variant | TDRD3 | GRCh38.p7 | 13:60432377 | TTACTAGCATTTTTA[-/C]CCTTACTAATCTTGT | 81550 |
rs5804003 | in-del | -/A | 0.193966 | 0.243639 | intron-variant, upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60438884 | GTTGATACTGATTAT[-/A]AAAAATGTGAGATAT | 81550 |
rs6562107 | snp | C/T | 0.26326 | 0.249648 | intron-variant | TDRD3 | GRCh38.p7 | 13:60403457 | GAAAGGTCTAGGATA[C/T]AGAAGTAGCCGAAGA | 81550 |
rs6562108 | snp | G/T | 0.486725 | 0.0803809 | intron-variant | TDRD3 | GRCh38.p7 | 13:60523234 | GCAGGTACAACTGCT[G/T]CTGGAGAATATTCTG | 81550 |
rs6650405 | snp | C/G | 0.21845 | 0.248001 | intron-variant | TDRD3 | GRCh38.p7 | 13:60521267 | GGTGTTAAACAGATA[C/G]CAATTTTGAACTTGG | 81550 |
rs7318738 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | TDRD3 | GRCh38.p7 | 13:60398388 | AGGGAGAGTTACTTT[C/G]CTAAAGTGGACTTGG | 81550 |
rs7319237 | snp | C/T | 0.497718 | 0.0614849 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419619 | gggaacatcacacac[C/T]gaggcctgttgtggg | 81550 |
rs7319865 | snp | C/G/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60516968 | AGGATAAAATTCAGA[C/G/T]TACATTATTTATATT | 81550 |
rs7322036 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TDRD3 | GRCh38.p7 | 13:60520518 | ccatttctccacaga[C/T]gttttccctctacat | 81550 |
rs7322160 | snp | C/T | 0.378174 | 0.214642 | intron-variant | TDRD3 | GRCh38.p7 | 13:60487322 | tctccactaaaatta[C/T]aaaattagctgggta | 81550 |
rs7322888 | snp | C/T | 0.481932 | 0.0933148 | intron-variant | TDRD3 | GRCh38.p7 | 13:60483644 | TGGTTTGAAATACTT[C/T]ATGGAAGGCCTTTTT | 81550 |
rs7323171 | snp | A/G | 0.0622301 | 0.165053 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395989 | ACTATGACTTTTGGG[A/G]AGACCAAACGGAATA | 81550 |
rs7323536 | snp | C/T | 0.188316 | 0.242271 | intron-variant | TDRD3 | GRCh38.p7 | 13:60425502 | acctagcaatcccta[C/T]tctgagtatatatcc | 81550 |
rs7325486 | snp | A/G | 0.175254 | 0.238565 | intron-variant | TDRD3 | GRCh38.p7 | 13:60399407 | AGTAGTAATCTGCGG[A/G]GCTAAAAACACTATC | 81550 |
rs7329723 | snp | A/G | 0.486133 | 0.082104 | intron-variant | TDRD3 | GRCh38.p7 | 13:60484590 | ACTGTCACCCTCTCT[A/G]AAAGCCTTTTGTAAG | 81550 |
rs7330768 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TDRD3 | GRCh38.p7 | 13:60435867 | tccgtagtggttgta[C/G]caatttacatttctg | 81550 |
rs7333390 | snp | A/C | 0.194902 | 0.243853 | intron-variant | TDRD3 | GRCh38.p7 | 13:60401199 | tctgtgggttctgca[A/C]ccttggattcaacca | 81550 |
rs7333682 | snp | A/G | 0.163564 | 0.234582 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432766 | TTTAAATTATCTTTT[A/G]TGTTTTTTCCCTCTC | 81550 |
rs7339393 | snp | C/T | 0.17461 | 0.238362 | intron-variant | TDRD3 | GRCh38.p7 | 13:60459643 | gttgttgtgttgaga[C/T]ggagtctcgctctgt | 81550 |
rs7981035 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | TDRD3 | GRCh38.p7 | 13:60550127 | GAGAGAGCTTAGAAA[A/G]ATAGTCTGTTTCAAA | 81550 |
rs7982963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TDRD3 | GRCh38.p7 | 13:60557274 | AGTGAAGGATGCAAA[C/G]CAATGGAGTTGGCTG | 81550 |
rs7986933 | snp | A/C | 0.213635 | 0.247341 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60395887 | GCGAACAGGATGGAG[A/C]TACTTGTGATCTAAA | 81550 |
rs7987793 | snp | C/G | 0 | 0 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60396227 | CAGTCTTCTTCCCCT[C/G]ACCTGGCAGATGGGG | 81550 |
rs7988525 | snp | A/T | 0.482609 | 0.0916147 | intron-variant | TDRD3 | GRCh38.p7 | 13:60544112 | AAATTCCTTTTTTTT[A/T]AAATTTTTTTCTGTC | 81550 |
rs7988922 | snp | A/G | 0.174288 | 0.23826 | intron-variant | TDRD3 | GRCh38.p7 | 13:60462974 | atccacatacttata[A/G]ccaactcactttcaa | 81550 |
rs7990171 | snp | A/G | 0.163564 | 0.234582 | intron-variant | TDRD3 | GRCh38.p7 | 13:60431481 | ATTTTTTAAATTTCC[A/G]TCTCaatttttaaaa | 81550 |
rs7990175 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558260 | ATTATGATATAATCA[C/T]TGCTCTCAGAGAAAG | 81550 |
rs7990196 | snp | A/G | 0.163892 | 0.234703 | intron-variant | TDRD3 | GRCh38.p7 | 13:60466392 | ATTTTTATTCTATTT[A/G]TCATGTCTTTATCAC | 81550 |
rs7993464 | snp | C/T | 0.364401 | 0.222289 | intron-variant | TDRD3 | GRCh38.p7 | 13:60563672 | CTCACTTGAGAACTC[C/T]TTCCTTAAAGGACTG | 81550 |
rs7994037 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TDRD3 | GRCh38.p7 | 13:60509413 | CTAGTATGGAGAAGT[A/G]TCAAAAAATTTCCAT | 81550 |
rs7994166 | snp | C/T | 0.463343 | 0.130326 | intron-variant | TDRD3 | GRCh38.p7 | 13:60558680 | ACTCAGACTTTATAG[C/T]GTGTCTGTAACTTTT | 81550 |
rs7994220 | snp | A/T | 0 | 0 | intron-variant | TDRD3 | GRCh38.p7 | 13:60414445 | aagcctgcaatattt[A/T]ctatctggttcttta | 81550 |
rs7995497 | snp | A/C | 0.189576 | 0.242588 | intron-variant | TDRD3 | GRCh38.p7 | 13:60479981 | tccttttaagtgtgt[A/C]atttaaccagtttac | 81550 |
rs7995827 | snp | A/C | 0.21875 | 0.248039 | intron-variant | TDRD3 | GRCh38.p7 | 13:60488614 | agtcttgctctgttg[A/C]ccagggtggagtgca | 81550 |
rs7996718 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TDRD3 | GRCh38.p7 | 13:60503292 | aaagttgtatagctt[C/G]attgtaacccatctt | 81550 |
rs7998592 | snp | C/T | 0.174288 | 0.23826 | intron-variant | TDRD3 | GRCh38.p7 | 13:60427565 | agagtttggtgatcc[C/T]ctctctacgtctttc | 81550 |
rs7999859 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | TDRD3 | GRCh38.p7 | 13:60455687 | CCTTTTGGGTGTATG[A/G]TTTGTTTCTAGGGTT | 81550 |
rs8002239 | snp | C/G | 0.248755 | 0.249997 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394606 | cttgaaccgggaggc[C/G]gaggttgcagtgagc | 81550 |
rs9317121 | snp | A/G | 0.121022 | 0.21416 | intron-variant | TDRD3 | GRCh38.p7 | 13:60565944 | CTTCTAACCATTTTG[A/G]GATTGATTGTTAATG | 81550 |
rs9528127 | snp | C/T | | | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394866 | ttctttggagttcag[C/T]gatgtcctgtgcttt | 81550 |
rs9528128 | snp | C/T | 0.494442 | 0.0524218 | upstream-variant-2KB | TDRD3 | GRCh38.p7 | 13:60394960 | cagattgtgacaacc[C/T]agacattgctaaatg | 81550 |
rs9528129 | snp | C/T | 0.489837 | 0.0705577 | intron-variant | TDRD3 | GRCh38.p7 | 13:60400692 | GCAGTGAGTCGAGAT[C/T]GCACCATTGCACTCC | 81550 |
rs9528130 | snp | C/T | 0.244205 | 0.249933 | intron-variant | TDRD3 | GRCh38.p7 | 13:60404411 | cgcctcccgggttca[C/T]gccattctcctgcct | 81550 |
rs9528131 | snp | C/T | 0.244205 | 0.249933 | intron-variant | TDRD3 | GRCh38.p7 | 13:60406127 | TCATCTAAAATAAGA[C/T]GTTAGGCATTAGGAA | 81550 |
rs9528132 | snp | G/T | 0.249886 | 0.25 | intron-variant | TDRD3 | GRCh38.p7 | 13:60410078 | ttctgcttttgcttc[G/T]tcctcatttttctct | 81550 |
rs9528133 | snp | A/G | 0.244205 | 0.249933 | intron-variant | TDRD3 | GRCh38.p7 | 13:60419209 | tccacttcctcacca[A/G]tattctattttcagt | 81550 |
rs9528134 | snp | A/G | 0.48679 | 0.0801892 | intron-variant | TDRD3 | GRCh38.p7 | 13:60430610 | TTTTAAATTTATGTG[A/G]AGTCATGGTTTACAA | 81550 |
rs9528135 | snp | C/T | 0.244205 | 0.249933 | intron-variant | TDRD3 | GRCh38.p7 | 13:60432764 | TTTTTAAATTATCTT[C/T]TATGTTTTTTCCCTC | 81550 |