SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13640 | snp | A/G | 0.178144 | 0.239451 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33837948 | TGAAGTTTTATTCCA[A/G]TTACTTTTCATGGAA | 6453 |
rs729960 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ITSN1 | GRCh38.p7 | 21:33824663 | GAGCTGCTCTGGGAG[C/T]GAGGCTGGGCCTGGT | 6453 |
rs730312 | snp | C/T | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33823929 | TCAGTATTAAGCTCT[C/T]TTCCTGCCTGTAACT | 6453 |
rs732687 | snp | A/G | 0.482979 | 0.0906686 | intron-variant | ITSN1 | GRCh38.p7 | 21:33879703 | CTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTCTT | 6453 |
rs743314 | snp | C/T | 0.108402 | 0.206034 | intron-variant | ITSN1 | GRCh38.p7 | 21:33855751 | GGCACAAGACCATCA[C/T]GGAGGCCAAGGCTGC | 6453 |
rs743315 | snp | A/G | 0.279726 | 0.248226 | intron-variant | ITSN1 | GRCh38.p7 | 21:33865539 | GGAGAGGAGGGGTGA[A/G]CCCTGGGCTTGGAAG | 6453 |
rs743316 | snp | A/G | 0.411914 | 0.190483 | intron-variant | ITSN1 | GRCh38.p7 | 21:33880392 | CCTGCTTGCCAAGAC[A/G]GGGTTCAAGCCACGT | 6453 |
rs762185 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | ITSN1 | GRCh38.p7 | 21:33854799 | CCTGTGCAAAAGTGC[A/G]AGCTCACCTTGCAGC | 6453 |
rs762186 | snp | A/T | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33870089 | CTTACATGTGACAAA[A/T]CTCCCTCCCACATAA | 6453 |
rs762187 | snp | A/G | 0.468047 | 0.122292 | intron-variant | ITSN1 | GRCh38.p7 | 21:33870186 | ATACTTAGTTTTGAA[A/G]TAAGTTTTCAACTTA | 6453 |
rs762240 | snp | A/G | 0.31014 | 0.242659 | intron-variant | ITSN1 | GRCh38.p7 | 21:33675372 | ACCGAGACCGTCCTA[A/G]CCAACACGGTGAAAC | 6453 |
rs879261 | snp | C/T | 0.499961 | 0.0043928 | intron-variant | ITSN1 | GRCh38.p7 | 21:33828460 | ACCGCCAGGTGCTTC[C/T]ATCCTGGTGGCCGAC | 6453 |
rs879262 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ITSN1 | GRCh38.p7 | 21:33828574 | GGAAATCTCGTCAGA[A/G]CATGAGAcctttttg | 6453 |
rs882363 | snp | C/T | 0.450231 | 0.149691 | intron-variant | ITSN1 | GRCh38.p7 | 21:33858114 | GGTGAGTGCTGCCCT[C/T]CTCCTGGGCTCTGGA | 6453 |
rs882364 | snp | A/C | 0.378765 | 0.214288 | intron-variant | ITSN1 | GRCh38.p7 | 21:33858029 | AGATCTCAGTGGAAC[A/C]CCGTGTTCCACTTGC | 6453 |
rs882365 | snp | A/G | 0.378568 | 0.214407 | intron-variant | ITSN1 | GRCh38.p7 | 21:33858026 | TCTCAGTGGAACCCC[A/G]TGTTCCACTTGCAAG | 6453 |
rs915537 | snp | C/G | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33771870 | ACAGTGTTTGGCGTG[C/G]AGGAGAAGATATAAA | 6453 |
rs915538 | snp | C/T | 0.344147 | 0.231595 | intron-variant | ITSN1 | GRCh38.p7 | 21:33783779 | TAAATATTAAGCTCT[C/T]TTCTGAACCCAGGCA | 6453 |
rs933130 | snp | C/G | 0.496637 | 0.0412629 | intron-variant | ITSN1 | GRCh38.p7 | 21:33875569 | CCCGGCAGAGCCTCG[C/G]CTGCCAGCCTGGAGG | 6453 |
rs964999 | snp | A/G | 0.318415 | 0.240457 | intron-variant | ITSN1 | GRCh38.p7 | 21:33698136 | GTAAGGATGATTTAG[A/G]AGAACTGAGGTTAAA | 6453 |
rs985926 | snp | C/T | 0.130008 | 0.219321 | intron-variant | ITSN1 | GRCh38.p7 | 21:33644959 | ccagagtatctggga[C/T]cacagatgcacgcca | 6453 |
rs1007429 | snp | C/T | 0.137527 | 0.223271 | intron-variant | ITSN1 | GRCh38.p7 | 21:33662347 | TCTGATTTAAAGTTC[C/T]GAATTTACAAATCCC | 6453 |
rs1007430 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | ITSN1 | GRCh38.p7 | 21:33664229 | gtcctcaggttgCTT[C/T]CACTCAGTGTGGACT | 6453 |
rs1048672 | snp | C/T | 0.252421 | 0.249988 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33837880 | CAGTAGACAACACCA[C/T]TGAGGTCGTTACGAT | 6453 |
rs1108000 | snp | A/G | 0.220272 | 0.248226 | synonymous-codon, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33829643 | GGTGGCGGTGTATGA[A/G]GCAATAACCTGGGCA | 6453 |
rs1109847 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | ITSN1 | GRCh38.p7 | 21:33857264 | GGGGGGCCATCTGGC[C/T]GCTGTCTCGAGTCAT | 6453 |
rs1109848 | snp | C/T | 0.3752 | 0.216391 | intron-variant | ITSN1 | GRCh38.p7 | 21:33857327 | CACTGAGAATGGCAA[C/T]GTTTCCTCCCAGGCC | 6453 |
rs1109849 | snp | C/G | 0.382279 | 0.212137 | intron-variant | ITSN1 | GRCh38.p7 | 21:33857371 | CTGACCTGAGTGATG[C/G]CTCCTCATCTTGTCA | 6453 |
rs1109850 | snp | A/C | 0.364609 | 0.222182 | intron-variant | ITSN1 | GRCh38.p7 | 21:33857589 | CGGGTGTGAAACCAT[A/C]TTGTCTGATAGTCTT | 6453 |
rs1125036 | snp | C/T | 0.45762 | 0.139261 | intron-variant | ITSN1 | GRCh38.p7 | 21:33658920 | cttattcataatgag[C/T]CCTTTTGGATCTTAT | 6453 |
rs1473800 | snp | A/C | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33706508 | CACTGGATATATTGA[A/C]CTTAAAATGAGTAAT | 6453 |
rs1475848 | snp | C/G | 0.279726 | 0.248226 | intron-variant | ITSN1 | GRCh38.p7 | 21:33861213 | ATTGTGCTGTATTTG[C/G]GTGGCTGCATAGACA | 6453 |
rs1537097 | snp | C/T | 0.332337 | 0.236052 | intron-variant | ITSN1 | GRCh38.p7 | 21:33790607 | AAAAAAATCACTTAA[C/T]TTTAGGAAGAACCGA | 6453 |
rs1537098 | snp | A/G | 0.40595 | 0.195396 | intron-variant | ITSN1 | GRCh38.p7 | 21:33852066 | GTACTGGGATTACAG[A/G]CATAAGCCACCAAGC | 6453 |
rs1547236 | snp | G/T | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33783909 | TTTGATAAATGTCTA[G/T]AAGATTAAATAATTT | 6453 |
rs1802358 | snp | C/T | 0.0402882 | 0.136092 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33838277 | CCCCTCGCGTTCTCC[C/T]GGCGCTGTCGGGAGG | 6453 |
rs1802359 | snp | C/T | 0.0414363 | 0.137845 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33838178 | TCTCAATAAAAATGC[C/T]TGCTGCTCACAGCAC | 6453 |
rs1802360 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33837770 | TGTAGCCACATGAGA[A/C]AGCACTCTGTGTTTT | 6453 |
rs1888449 | snp | A/G | 0.442791 | 0.15916 | | | GRCh38.p7 | 21:33858960 | CCCTTTTGTGCCTTC[A/G]TGCTTTCTGGAAACG | 6453 |
rs1892587 | snp | A/C | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 21:33732123 | GCTGGAATCAATAGA[A/C]GGGAATGTGTGGGTT | 6453 |
rs1892588 | snp | A/G | 0.4776 | 0.103433 | | | GRCh38.p7 | 21:33788837 | CTGGTACAGTGACAT[A/G]TATCTCAGGAGGCTG | 6453 |
rs1892589 | snp | A/T | 0.314301 | 0.241589 | | | GRCh38.p7 | 21:33793719 | TACTTTTAACCTGAT[A/T]GCTGGTTTAGTTTGG | 6453 |
rs1892700 | snp | A/G | 0.288906 | 0.246954 | | | GRCh38.p7 | 21:33643831 | CAAGGCCAATGAAGA[A/G]GGTAGATAATAACAG | 6453 |
rs2000461 | snp | A/G | 0.430136 | 0.173352 | intron-variant | ITSN1 | GRCh38.p7 | 21:33647071 | CTAGACTAAACATTG[A/G]AAGTATTTAATAAGC | 6453 |
rs2007477 | snp | A/G | 0.314787 | 0.241459 | intron-variant | ITSN1 | GRCh38.p7 | 21:33824264 | CCTAAAAATTTGATC[A/G]CATAAACTGTGGTCT | 6453 |
rs2040121 | snp | G/T | 0.460252 | 0.135255 | intron-variant | ITSN1 | GRCh38.p7 | 21:33774273 | TGAATGATTAGGAAG[G/T]GGGGAGTCGCAGACT | 6453 |
rs2070391 | snp | C/T | 0.261056 | 0.249755 | intron-variant | ITSN1 | GRCh38.p7 | 21:33654836 | GAGAACACTACCTGA[C/T]TCTCTGACAGCATTA | 6453 |
rs2070392 | snp | A/G | 0.209693 | 0.246729 | intron-variant | ITSN1 | GRCh38.p7 | 21:33655384 | CTGTATAGGGGGTGA[A/G]TCTGAATTCTGTTCA | 6453 |
rs2070393 | snp | A/G | 0.457737 | 0.139088 | intron-variant | ITSN1 | GRCh38.p7 | 21:33866783 | CCCAGAGGCACGTGC[A/G]GGCTCCACTCAAAAC | 6453 |
rs2070394 | snp | A/T | 0.443195 | 0.158668 | intron-variant | ITSN1 | GRCh38.p7 | 21:33867101 | AGTCAGGCCCTTCCA[A/T]CCCCAGGTCTCTCAG | 6453 |
rs2073366 | snp | C/G | 0.378174 | 0.214642 | intron-variant | ITSN1 | GRCh38.p7 | 21:33858617 | TCCCTGCTCTCAGCG[C/G]ATCGGCGTGTGAGTG | 6453 |
rs2073367 | snp | C/T | 0.133926 | 0.22142 | intron-variant | ITSN1 | GRCh38.p7 | 21:33858683 | CGTTTTCTGCATCTG[C/T]AGATTTTTCAAAAAC | 6453 |
rs2073368 | snp | G/T | 0.235411 | 0.249574 | intron-variant | ITSN1 | GRCh38.p7 | 21:33794499 | ATTGTGGACTCATCT[G/T]GAAGGAACTTTGAGG | 6453 |
rs2073369 | snp | A/G | 0.329317 | 0.237084 | intron-variant | ITSN1 | GRCh38.p7 | 21:33794641 | ATCTTTGCATGTATC[A/G]GTACCCTCTGAAGTT | 6453 |
rs2073370 | snp | C/T | 0.488246 | 0.0757536 | synonymous-codon, nc-transcript-variant | ITSN1 | GRCh38.p7 | 21:33888177 | TCGGACGGAGATCCG[C/T]GTGGCGGACATCAAG | 6453 |
rs2096465 | snp | G/T | 0.483995 | 0.0880135 | intron-variant | ITSN1 | GRCh38.p7 | 21:33878312 | TGCTGGGATTACAGG[G/T]GTGAGCCACCACGCC | 6453 |
rs2154432 | snp | A/G | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33687523 | TGTTTCTAATCTGTA[A/G]AACTTGAAGGCCTAA | 6453 |
rs2154433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ITSN1 | GRCh38.p7 | 21:33729989 | TGTTTTTAAACAGAG[A/G]ACATATAAAGTACTA | 6453 |
rs2154434 | snp | A/C | 0.499964 | 0.00422623 | intron-variant | ITSN1 | GRCh38.p7 | 21:33755430 | TTAGTGAAATATGAT[A/C]TTTGTTTTCAATGTA | 6453 |
rs2156398 | snp | A/C | | | intron-variant | ITSN1 | GRCh38.p7 | 21:33844898 | TAGGGGGCAGAAGCA[A/C]ATCTGCCCGTCCTGT | 6453 |
rs2186281 | snp | A/C | 0.345704 | 0.230956 | intron-variant | ITSN1 | GRCh38.p7 | 21:33792857 | TCTGCTAGGTTCCCT[A/C]CTGAAGCCCCTTCTT | 6453 |
rs2211689 | snp | C/T | 0.317692 | 0.240661 | intron-variant | ITSN1 | GRCh38.p7 | 21:33677768 | tgtctttgattccgc[C/T]cttccaccactttat | 6453 |
rs2211690 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ITSN1 | GRCh38.p7 | 21:33741749 | TACAAAAAAAAATTA[A/G]CCAAGCATGGTGGCG | 6453 |
rs2236613 | snp | C/T | 0.230116 | 0.249208 | intron-variant, downstream-variant-500B | ITSN1 | GRCh38.p7 | 21:33818498 | ATTTATCTGCTTGTA[C/T]TTGATGAAAACAATA | 6453 |
rs2243871 | snp | C/G | 0.401037 | 0.199218 | intron-variant | ITSN1 | GRCh38.p7 | 21:33878422 | CCATTTTTTCTCTCT[C/G]TTTCTGTATACACAT | 6453 |
rs2244151 | snp | G/T | 0.499997 | 0.00119808 | intron-variant | ITSN1 | GRCh38.p7 | 21:33821091 | TGCTACTTTTATGTC[G/T]TTTTTGCTTCATTCC | 6453 |
rs2244270 | snp | G/T | 0.286303 | 0.24735 | intron-variant | ITSN1 | GRCh38.p7 | 21:33822534 | CCTGTACCTAGAACC[G/T]CCATCCAGGATTTTG | 6453 |
rs2244966 | snp | A/G | 0.465473 | 0.126772 | intron-variant | ITSN1 | GRCh38.p7 | 21:33755055 | TTGAAACAGCCTCTC[A/G]GTCTATTGTGTTTAT | 6453 |
rs2245099 | snp | A/G | 0.219615 | 0.248147 | intron-variant | ITSN1 | GRCh38.p7 | 21:33828977 | CTCCAGGTCCCTCCT[A/G]TAACGTGAAATAAAA | 6453 |
rs2246299 | snp | C/T | 0.371987 | 0.218218 | intron-variant | ITSN1 | GRCh38.p7 | 21:33792445 | TTAAGTATAGTCTTT[C/T]GCTGTAAATTATTTT | 6453 |
rs2246647 | snp | C/T | 0.473359 | 0.112298 | intron-variant | ITSN1 | GRCh38.p7 | 21:33795725 | TTTATAAAATGCTTT[C/T]ATTATTCACACTATA | 6453 |
rs2248321 | snp | A/G | 0.499984 | 0.00279548 | intron-variant | ITSN1 | GRCh38.p7 | 21:33834576 | CCCAACTAATGTGAT[A/G]TGGAATATGTCTTTC | 6453 |
rs2248815 | snp | A/G | 0.262677 | 0.249678 | intron-variant | ITSN1 | GRCh38.p7 | 21:33766022 | TTTTAGGTAAGGAAC[A/G]TGGGCTCTGATCAGG | 6453 |
rs2249221 | snp | G/T | 0.489722 | 0.0709447 | intron-variant | ITSN1 | GRCh38.p7 | 21:33853831 | TGGAGTGGGATGCAG[G/T]GCAAACCTCAGCCTT | 6453 |
rs2250452 | snp | G/T | 0.359972 | 0.247671 | intron-variant | ITSN1 | GRCh38.p7 | 21:33804593 | CTAAGGCTTAGATGC[G/T]TAGAAAATACATGGC | 6453 |
rs2251854 | snp | A/G | 0.475081 | 0.108804 | intron-variant | ITSN1 | GRCh38.p7 | 21:33683942 | GCTTGTTTGCTATTG[A/G]AGCCGATGCCCCTAA | 6453 |
rs2254480 | snp | A/G | 0.435263 | 0.167862 | intron-variant | ITSN1 | GRCh38.p7 | 21:33814439 | ATGTATTTAAGGAAA[A/G]TCACATACCCCTCCA | 6453 |
rs2256797 | snp | C/T | 0.288646 | 0.246995 | intron-variant | ITSN1 | GRCh38.p7 | 21:33785207 | AGTTGATCAGGATAC[C/T]AAATCTATATTAAGT | 6453 |
rs2268243 | snp | A/G | | | intron-variant | ITSN1 | GRCh38.p7 | 21:33792507 | GAAAATGAAATTTTC[A/G]TTCATATTATTACTG | 6453 |
rs2268244 | snp | A/G | | | intron-variant | ITSN1 | GRCh38.p7 | 21:33792519 | TTCATTCATATTATT[A/G]CTGATTATTTATTCT | 6453 |
rs2268245 | snp | A/G | | | intron-variant | ITSN1 | GRCh38.p7 | 21:33792523 | TTCATATTATTACTG[A/G]TTATTTATTCTTGAT | 6453 |
rs2268246 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ITSN1 | GRCh38.p7 | 21:33804112 | TAGGTTGAAAAATCC[A/G]GGGTTCACTTATACT | 6453 |
rs2268247 | snp | C/T | 0.323671 | 0.238899 | intron-variant | ITSN1 | GRCh38.p7 | 21:33804666 | ATCAAATTTGACATC[C/T]GTAACATGTTAGTAG | 6453 |
rs2268248 | snp | A/G | 0.285519 | 0.247464 | intron-variant | ITSN1 | GRCh38.p7 | 21:33814796 | TGCCACCAGTCAGGG[A/G]GCTGTTGGTGTCACC | 6453 |
rs2268249 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | ITSN1 | GRCh38.p7 | 21:33816377 | TACTAAACTTCCTTC[C/T]CCCTCCCCACCTACA | 6453 |
rs2268250 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ITSN1 | GRCh38.p7 | 21:33822691 | AAGACACAAAGGAAC[A/G]TTAGTTCTTATCCTT | 6453 |
rs2268251 | snp | G/T | 0.307176 | 0.243374 | intron-variant | ITSN1 | GRCh38.p7 | 21:33846580 | AAACCAGAGGGCAGG[G/T]CCTACCTCCCACACG | 6453 |
rs2268252 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ITSN1 | GRCh38.p7 | 21:33846761 | CATTCTCCCTGCTGC[A/G]TGTAGCCTGGAACCC | 6453 |
rs2268253 | snp | A/G | 0.394904 | 0.203722 | intron-variant | ITSN1 | GRCh38.p7 | 21:33846811 | AGTTTCCCTCCCCAG[A/G]AGGAAAGGAAATTGT | 6453 |
rs2268254 | snp | C/T | 0.308414 | 0.24308 | intron-variant | ITSN1 | GRCh38.p7 | 21:33853890 | CATGGTGGGGAAGAG[C/T]ACCACCTTCAGCGGA | 6453 |
rs2268255 | snp | A/C | 0.434253 | 0.168969 | intron-variant | ITSN1 | GRCh38.p7 | 21:33853957 | GTCCCCCAGGTTCTT[A/C]GCTATGCCCTGGAGG | 6453 |
rs2268256 | snp | A/G | 0.41507 | 0.187755 | intron-variant | ITSN1 | GRCh38.p7 | 21:33860656 | TACGGCTGAAGCAGC[A/G]AAGCTCAGAGAGGCT | 6453 |
rs2268257 | snp | A/G | 0.400325 | 0.199756 | intron-variant | ITSN1 | GRCh38.p7 | 21:33864163 | TCAAAGGCTTCTCCA[A/G]CATGACCATGAAAGC | 6453 |
rs2276227 | snp | A/G | 0.330016 | 0.236849 | intron-variant | ITSN1 | GRCh38.p7 | 21:33750420 | TCTGATTATGTTTAA[A/G]TGATATTTTAGTCCA | 6453 |
rs2282468 | snp | A/G | 0.373799 | 0.217195 | intron-variant | ITSN1 | GRCh38.p7 | 21:33856255 | AGGAGTGTGCCGCCT[A/G]TATCAGTTTCTAGGG | 6453 |
rs2282469 | snp | C/T | 0.40853 | 0.193309 | intron-variant | ITSN1 | GRCh38.p7 | 21:33857115 | TCCCTGAGCAGTTGA[C/T]GGATGGAGTCATGTG | 6453 |
rs2282470 | snp | A/G | 0.115438 | 0.210697 | intron-variant | ITSN1 | GRCh38.p7 | 21:33857215 | GGAGCCAGCCACGCC[A/G]CCCTCCTGGCCCGCA | 6453 |
rs2284561 | snp | A/G | 0.28052 | 0.24813 | intron-variant | ITSN1 | GRCh38.p7 | 21:33698724 | TCTGTGTTTTAAAAG[A/G]GCTTTGTGTACCTCT | 6453 |
rs2284562 | snp | A/G | 0.268724 | 0.249298 | intron-variant | ITSN1 | GRCh38.p7 | 21:33727395 | ATGGAGAGAAAAGAG[A/G]GAGTGAGGGAGCACT | 6453 |
rs2284563 | snp | A/G | 0 | 0 | intron-variant | ITSN1 | GRCh38.p7 | 21:33771504 | GGATAGAACTGAGTA[A/G]TCATTCTAAATTTAT | 6453 |