SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15834 | snp | G/T | 0.282632 | 0.247861 | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53462504 | TATATAAACAAAATA[G/T]CCATATCTGATTTTT | 84708 |
rs366074 | snp | C/G | 0.305685 | 0.24372 | intron-variant | LNX1 | GRCh38.p7 | 4:53565967 | AGAATAAAAAGAAAC[C/G]AGCAAAGCCTCCAAG | 84708 |
rs716251 | snp | A/T | 0.265727 | 0.249505 | intron-variant | LNX1 | GRCh38.p7 | 4:53555893 | GTAGAAGAGAAAATT[A/T]TTAAGTGGTATAAGG | 84708 |
rs727943 | snp | A/C | 0.248784 | 0.253684 | intron-variant | LNX1 | GRCh38.p7 | 4:53556272 | AGGAACACCTGCAGC[A/C]CCCCCCTCCACAAAA | 84708 |
rs750695 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | LNX1 | GRCh38.p7 | 4:53637601 | TTGTTTCATTACTAC[A/G]GAATTTCATCACTTC | 84708 |
rs769072 | snp | A/C | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53530816 | CAAATTACATAGTGT[A/C]TAGAATTTGCTTTAA | 84708 |
rs907505 | snp | A/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53637616 | ccctttggcatctta[A/G]aagtgatgaaatTCT | 84708 |
rs907506 | snp | G/T | 0.0825414 | 0.185628 | intron-variant | LNX1 | GRCh38.p7 | 4:53531376 | TTTTCCAGAGCCACA[G/T]TCCTCTCATCTATAA | 84708 |
rs907509 | snp | A/C | 0.418007 | 0.185132 | intron-variant | LNX1 | GRCh38.p7 | 4:53587231 | CTTTCTGTGTTTACC[A/C]TTTCCTCCATTTTGT | 84708 |
rs907510 | snp | G/T | 0.28052 | 0.24813 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53603251 | GACTCCTCACTGCAT[G/T]TGAGGACCTACTCAT | 84708 |
rs907511 | snp | G/T | 0.38286 | 0.211774 | intron-variant | LNX1 | GRCh38.p7 | 4:53572599 | GAAATTTGGAAGATG[G/T]TGTTTATCCTGGTTC | 84708 |
rs925477 | snp | C/T | 0.38286 | 0.211774 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53596501 | TGTTTATAATGGTCA[C/T]GAGACCTATATCTTA | 84708 |
rs925664 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53519046 | ATGAGGCATGCAGCA[A/C]TGATAAATGGCCCTG | 84708 |
rs932038 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | LNX1 | GRCh38.p7 | 4:53585079 | TTCACTTCCAGGTAC[A/G]GGTTTTCAAAGGGAC | 84708 |
rs932039 | snp | A/G | 0.220843 | 0.248294 | intron-variant | LNX1 | GRCh38.p7 | 4:53585008 | CCATCTGGACTACCC[A/G]GGAAGACAATTGGAA | 84708 |
rs932040 | snp | A/T | 0.35574 | 0.226537 | intron-variant | LNX1 | GRCh38.p7 | 4:53582727 | GCATCATCAACAATT[A/T]AAAAAAAAACAAAAA | 84708 |
rs959094 | snp | C/T | 0.460813 | 0.134379 | intron-variant | LNX1 | GRCh38.p7 | 4:53617402 | TCCCAAAGTAAATTT[C/T]CTTTTCTGGATATTA | 84708 |
rs967018 | snp | A/G | 0.128632 | 0.218563 | intron-variant | LNX1 | GRCh38.p7 | 4:53478244 | TCTAAGTGGTTCTTT[A/G]GTGGGTTGATCCGGT | 84708 |
rs979006 | snp | A/G | 0.247905 | 0.249991 | intron-variant | LNX1 | GRCh38.p7 | 4:53586711 | AAGAAGGGCAAAGGC[A/G]AAGAGAACAAGAGTA | 84708 |
rs1002824 | snp | A/C | 0.391769 | 0.205917 | intron-variant | LNX1 | GRCh38.p7 | 4:53579813 | AGTTGCCAGAATAAA[A/C]CACATACTCCACTAG | 84708 |
rs1013928 | snp | A/C | 0.499784 | 0.0103811 | intron-variant | LNX1 | GRCh38.p7 | 4:53649344 | GTCAATCCCACAAGG[A/C]GACTACTATTACAAT | 84708 |
rs1014056 | snp | C/T | 0.337841 | 0.23406 | intron-variant, utr-variant-3-prime, downstream-variant-500B | LNX1, FIP1L1 | GRCh38.p7 | 4:53459823 | TCTTAAGAGGCTGCA[C/T]CACAAAAGGCAACAA | 84708 |
rs1015801 | snp | A/G | 0.240478 | 0.249819 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53595381 | AGTCAACAGGCATGT[A/G]AGGACATGAAGCAGT | 84708 |
rs1022187 | snp | C/G | 0.306431 | 0.243548 | intron-variant | LNX1 | GRCh38.p7 | 4:53651408 | TGGGCATTGAATTCA[C/G]TTCAACAAATGTCGA | 84708 |
rs1028000 | snp | C/T | 0.354665 | 0.227036 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594364 | GGTCATTTTTCTCTG[C/T]AACTTCTGCGGCCTA | 84708 |
rs1036379 | snp | A/G | 0.117188 | 0.211804 | intron-variant | LNX1 | GRCh38.p7 | 4:53553659 | CATGGAGGTCTGCGG[A/G]TGAGGGCATGTGGGG | 84708 |
rs1040084 | snp | A/G | 0.361684 | 0.223667 | intron-variant | LNX1 | GRCh38.p7 | 4:53544057 | GTCTTCTTCACCTTC[A/G]CTGTCCTATTTTTGA | 84708 |
rs1077966 | snp | C/T | 0.251296 | 0.249997 | intron-variant | LNX1 | GRCh38.p7 | 4:53651174 | TGGACTTGGTGTAAG[C/T]AAATGTTCACTCAAC | 84708 |
rs1125349 | snp | A/G | 0.499776 | 0.0105807 | intron-variant | LNX1 | GRCh38.p7 | 4:53649343 | TGTCAATCCCACAAG[A/G]CGACTACTATTACAA | 84708 |
rs1126328 | snp | C/T | 0.268452 | 0.249318 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53595556 | TTAGGAGCAAGCCTC[C/T]TTTGCAGTCAACATA | 84708 |
rs1212751 | snp | A/G | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510973 | AGATTATGCCATTAA[A/G]AAACCATTGCACTTT | 84708 |
rs1347406 | snp | A/G | 0.402277 | 0.198272 | intron-variant | LNX1 | GRCh38.p7 | 4:53586320 | CACGTGACTGTCAAA[A/G]GCAGTCATAAGCAAG | 84708 |
rs1369351 | snp | C/T | 0.269267 | 0.249256 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53596785 | CATCCCTGACTTCCC[C/T]CTATTATAATGACAA | 84708 |
rs1369352 | snp | C/G | 0.370772 | 0.218893 | intron-variant | LNX1 | GRCh38.p7 | 4:53530885 | TGAGTCACTATGCCT[C/G]GCCTCATTTTACAAT | 84708 |
rs1369353 | snp | A/G | 0.447032 | 0.153878 | intron-variant | LNX1 | GRCh38.p7 | 4:53530794 | TGTAATTTGACCCTG[A/G]AATACTTAAACAAAA | 84708 |
rs1369354 | snp | A/C | 0.403334 | 0.197456 | intron-variant | LNX1 | GRCh38.p7 | 4:53581807 | ATCAAAAACAAGATG[A/C]GTGATATGGTTTGGC | 84708 |
rs1369355 | snp | C/T | 0.402806 | 0.197864 | intron-variant | LNX1 | GRCh38.p7 | 4:53580693 | CACCTAATGCCACTA[C/T]ATATTTTTGCATTTT | 84708 |
rs1398157 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | LNX1 | GRCh38.p7 | 4:53524716 | TTTAGGGGAAATAAA[A/C]ATAGTTGAGCCATTT | 84708 |
rs1398158 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | LNX1 | GRCh38.p7 | 4:53526202 | AAACCCCATCACTGG[A/G]CACGGCACACTGCTC | 84708 |
rs1399241 | snp | C/T | 0.455977 | 0.141681 | intron-variant | LNX1 | GRCh38.p7 | 4:53483140 | ATCTCGAGAACAGCA[C/T]GGGAAAGACCCACCC | 84708 |
rs1435210 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513277 | ATGTATTATGCTTTA[C/T]GGATGTGGTCTCATT | 84708 |
rs1435211 | snp | A/G | 0.275464 | 0.2487 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513278 | TGTATTATGCTTTAT[A/G]GATGTGGTCTCATTT | 84708 |
rs1435212 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513353 | ATGAAGATATGGACA[C/G]TAGAAGGGAGAAATG | 84708 |
rs1435213 | snp | A/C | 0.0955749 | 0.196603 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514905 | GAACATTTAACTGAC[A/C]AATTAGGCTAAACAT | 84708 |
rs1435214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LNX1 | GRCh38.p7 | 4:53590733 | TGTAACCAAAGGTCA[A/G]CAGGCAGCCAGTCCA | 84708 |
rs1435215 | snp | C/T | 0.334871 | 0.235153 | intron-variant | LNX1 | GRCh38.p7 | 4:53545367 | TTCACACCTTTATAA[C/T]TCAGTAGGGCCAGGT | 84708 |
rs1435216 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | LNX1 | GRCh38.p7 | 4:53545221 | TCCTAGTTTGTATAA[C/T]TATTTTCCCATTGAA | 84708 |
rs1435217 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | LNX1 | GRCh38.p7 | 4:53545210 | ATAACTATTTTCCCA[C/T]TGAAGTAGGCATAAG | 84708 |
rs1435218 | snp | A/G | 0.159951 | 0.233219 | intron-variant | LNX1 | GRCh38.p7 | 4:53535732 | GCAGGGAATAGACTA[A/G]GAAGTACATGGCATA | 84708 |
rs1435219 | snp | C/T | 0.45692 | 0.1403 | intron-variant | LNX1 | GRCh38.p7 | 4:53535682 | AGCCAAGAAACTCAA[C/T]TCATTTCCCTGGCTC | 84708 |
rs1435220 | snp | A/G | 0.333952 | 0.235483 | intron-variant | LNX1 | GRCh38.p7 | 4:53535586 | ACATTTACCTCTGAG[A/G]ACATTAATGCAGAGT | 84708 |
rs1435221 | snp | C/T | 0.44651 | 0.154543 | intron-variant | LNX1 | GRCh38.p7 | 4:53532609 | GAGGAGAATTTCCTA[C/T]GGGGACTATCAAAAT | 84708 |
rs1435222 | snp | A/G | 0.489492 | 0.0717183 | intron-variant | LNX1 | GRCh38.p7 | 4:53530223 | TGTATATTTTAAAAC[A/G]TTACTTAAAAATAAT | 84708 |
rs1435223 | snp | A/T | 0.31503 | 0.241394 | intron-variant | LNX1 | GRCh38.p7 | 4:53530046 | TAATTTTTACTTGAT[A/T]AAACATATCAAACTT | 84708 |
rs1435224 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510076 | GACAAGCAAATGTTT[C/T]ATCTGCTTAGAAAGA | 84708 |
rs1435225 | snp | C/T | 0.380333 | 0.213338 | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53577610 | CTGGTCAACATAGCA[C/T]GACCCCATCTTTAAA | 84708 |
rs1464028 | snp | A/C | 0.406814 | 0.194704 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594657 | TAGCAGTTGGTTTTA[A/C]CCCCCAAGATCAAAC | 84708 |
rs1467156 | snp | G/T | 0.497121 | 0.0378299 | intron-variant | LNX1 | GRCh38.p7 | 4:53472685 | gtttttttttttttt[G/T]ttgttgttgttgttg | 84708 |
rs1477873 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | LNX1 | GRCh38.p7 | 4:53644659 | AGTCACCTGACATGG[A/C]ATCCCGCTCCCTCCT | 84708 |
rs1477875 | snp | A/G | 0.302435 | 0.244439 | intron-variant | LNX1 | GRCh38.p7 | 4:53626338 | GGTTGCATAACCCTC[A/G]TATAATAAATATACT | 84708 |
rs1477876 | snp | C/T | 0.279195 | 0.248289 | intron-variant | LNX1 | GRCh38.p7 | 4:53616053 | AGAGTCTTGGAAGGA[C/T]GGGGGTGGTGAGGAG | 84708 |
rs1514387 | snp | A/C | 0.126909 | 0.217598 | intron-variant | LNX1 | GRCh38.p7 | 4:53483865 | ATAGCAGGCAGGAAG[A/C]AAATATCTCCACCAC | 84708 |
rs1514388 | snp | A/C | 0.126909 | 0.217598 | intron-variant | LNX1 | GRCh38.p7 | 4:53483851 | GAAAATATCTCCACC[A/C]CCATTGTCTGAGTCA | 84708 |
rs1514389 | snp | C/G | 0.128288 | 0.218372 | intron-variant | LNX1 | GRCh38.p7 | 4:53483832 | TTGTCTGAGTCAATG[C/G]AAAAGAGCATGGAAT | 84708 |
rs1541967 | snp | G/T | 0.468949 | 0.12067 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515952 | ATTTACCATGAGGTT[G/T]AAAGATTCGCACAAA | 84708 |
rs1546526 | snp | A/G | 0.293551 | 0.246177 | intron-variant | LNX1 | GRCh38.p7 | 4:53633084 | GATTTAAGCAGCTAA[A/G]AAGTGATGATGTTGG | 84708 |
rs1546527 | snp | C/G | 0.445855 | 0.155373 | intron-variant | LNX1 | GRCh38.p7 | 4:53631120 | CTTAACTCCATGGGC[C/G]ACTTCCTCCTCCTCT | 84708 |
rs1567654 | snp | A/G | 0.421209 | 0.182174 | intron-variant | LNX1 | GRCh38.p7 | 4:53582010 | AAAATTTAAGGTGCA[A/G]AAAAATTCAGTAATC | 84708 |
rs1812717 | snp | C/T | 0.474634 | 0.109726 | intron-variant | LNX1 | GRCh38.p7 | 4:53526887 | AAACATCGTGAGCCT[C/T]CTGTGGAGCCAGCTG | 84708 |
rs1858389 | snp | A/C | 0.0908922 | 0.192833 | intron-variant | LNX1 | GRCh38.p7 | 4:53524782 | CAGTAGCTGGATGTT[A/C]AATTCCTCAGTTCCT | 84708 |
rs1865509 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512976 | CCAACTCCATCTCCA[C/T]GGCCAAACCCTGGAG | 84708 |
rs1865510 | snp | A/G | 0.208779 | 0.246578 | intron-variant | LNX1 | GRCh38.p7 | 4:53488659 | TCCAAAAACTCAATC[A/G]ATTCCTGTCTTTACC | 84708 |
rs1903827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LNX1 | GRCh38.p7 | 4:53634600 | TTTCCTCTGGGAGTA[C/T]CATCTCTACTGGTGG | 84708 |
rs1913484 | snp | A/G | 0.43978 | 0.162738 | intron-variant | LNX1 | GRCh38.p7 | 4:53544157 | TTGAGAGCAGTACAT[A/G]GAAATTAGTAAGCAC | 84708 |
rs1913485 | snp | A/G | 0.43655 | 0.16643 | intron-variant | LNX1 | GRCh38.p7 | 4:53544264 | CAGTGGTGCCATCTC[A/G]GCTCACTGCAGCCTC | 84708 |
rs1913486 | snp | A/C | 0.327445 | 0.237702 | intron-variant | LNX1 | GRCh38.p7 | 4:53544426 | TCTCAAACTACTGAA[A/C]TCAGGTGATCCACCC | 84708 |
rs1965112 | snp | A/G | 0.349452 | 0.229367 | intron-variant | LNX1 | GRCh38.p7 | 4:53620628 | GAAATCCGGGACTTC[A/G]GTGCATCCATCAGTG | 84708 |
rs1972815 | snp | A/G | 0.324382 | 0.238678 | intron-variant | LNX1 | GRCh38.p7 | 4:53620367 | gatcccactcccagc[A/G]tttgtaattctttac | 84708 |
rs1978767 | snp | A/G | 0.334182 | 0.235401 | intron-variant | LNX1 | GRCh38.p7 | 4:53534601 | agactagagtacagt[A/G]gtgtgaccatagctc | 84708 |
rs1991972 | snp | A/C | 0.487113 | 0.0792303 | intron-variant | LNX1 | GRCh38.p7 | 4:53636286 | ACAAAACTTCATTGT[A/C]TTGAAAAAATTAGCA | 84708 |
rs1991973 | snp | A/G | 0.499295 | 0.0187567 | intron-variant | LNX1 | GRCh38.p7 | 4:53636319 | CACCTCCTTCCACAC[A/G]TCACTGTGGTAAGAA | 84708 |
rs1996005 | snp | A/T | 0.294576 | 0.245994 | intron-variant | LNX1 | GRCh38.p7 | 4:53640828 | AACCTCTTGTGAGAA[A/T]TAGTCAATGCACAAT | 84708 |
rs2033618 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53602631 | TTACACGTGGTGACT[A/G]AACTAATGAAGTAGC | 84708 |
rs2048511 | snp | C/T | 0.283684 | 0.24772 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53595776 | GATCCCCCCATGAAG[C/T]TTGGCGTTCTCAAGG | 84708 |
rs2048709 | snp | C/T | 0.338363 | 0.233863 | intron-variant, downstream-variant-500B, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53460228 | GCATGAGTTTTTATA[C/T]AGTTACTAACGATTG | 84708 |
rs2048710 | snp | A/G | 0.363985 | 0.222503 | intron-variant | LNX1 | GRCh38.p7 | 4:53540466 | CTTGTAAGAAAGCTT[A/G]TTAAAAATAAGTGTT | 84708 |
rs2082768 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | LNX1 | GRCh38.p7 | 4:53564544 | aataattattcccca[A/G]agatgtccagctcct | 84708 |
rs2082769 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | LNX1 | GRCh38.p7 | 4:53564548 | attattccccagaga[C/T]gtccagctcctaatc | 84708 |
rs2099452 | snp | C/T | 0.227959 | 0.249026 | upstream-variant-2KB, intron-variant | LNX1, LNX1-AS2 | GRCh38.p7 | 4:53592914 | GCCGGCTCTGGTGCT[C/T]GACCTCAGGGGAGCT | 84708 |
rs2099453 | snp | C/T | 0.494855 | 0.0504572 | intron-variant | LNX1 | GRCh38.p7 | 4:53564319 | ACAGAGTTCCAACAG[C/T]CACCTGCTAGCCCTT | 84708 |
rs2117596 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511450 | ACTAAGTACTCTCAG[A/G]TGGTGATGGGTGATG | 84708 |
rs2117597 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511521 | CCCTTTTCAACCAAA[A/G]CACAAGCTTTGGAGG | 84708 |
rs2117598 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511808 | TTCTGATAGGGTATC[A/C]TCTGCAAAGGTCACC | 84708 |
rs2117599 | snp | A/G | 0.478271 | 0.101943 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599120 | TGGCATGTGAACCAG[A/G]GCAATTCATCTTGAA | 84708 |
rs2117600 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | LNX1 | GRCh38.p7 | 4:53551507 | GTATATGAATCCTCA[A/G]CTGATAAGGAGAAAA | 84708 |
rs2117601 | snp | A/G | 0.43309 | 0.17023 | intron-variant | LNX1 | GRCh38.p7 | 4:53551705 | aaggtcaaaccaccc[A/G]gctgatctcaagtca | 84708 |
rs2137896 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | LNX1 | GRCh38.p7 | 4:53482600 | tgattttccattcct[C/G]tgttacttcacttaa | 84708 |
rs2164265 | snp | A/G | 0.275464 | 0.2487 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511373 | AGGACAAGAACATAC[A/G]GTAAACCCTGGGTTG | 84708 |
rs2164266 | snp | G/T | 0.288646 | 0.246995 | intron-variant | LNX1 | GRCh38.p7 | 4:53630096 | ATTAAAAAAAGGTGG[G/T]GGGGGCATGCGGGTG | 84708 |
rs2164267 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53636590 | GTGTCAAAACAGTTA[C/T]ACAAAATGACCAGCA | 84708 |
rs2175552 | snp | C/G | 0.478685 | 0.10101 | intron-variant | LNX1 | GRCh38.p7 | 4:53610190 | CATTACTCTGAATTT[C/G]CTCAAGTTTTCTTTG | 84708 |
rs2253608 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LNX1 | GRCh38.p7 | 4:53620099 | CCTCACTTGCTGCTG[A/G]CACAGACAGGATAAA | 84708 |
rs2257185 | snp | A/G | 0.325091 | 0.238456 | intron-variant | LNX1 | GRCh38.p7 | 4:53610408 | CTGTGAAAACTATAT[A/G]TGAAAAATTTTGTAG | 84708 |
rs2271556 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502138 | ATAGTAAACTCTCAG[G/T]TAATAATTATTATTA | 84708 |
rs2271557 | snp | A/G | 0.251014 | 0.249998 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502063 | TTTCTTTCCAGACCA[A/G]TACAGAAGATGAGGT | 84708 |
rs2271558 | snp | C/T | 0.499958 | 0.00459246 | intron-variant | LNX1 | GRCh38.p7 | 4:53496666 | AACAGAAATGAAGGC[C/T]AGGATTCTGGGAATA | 84708 |
rs2271559 | snp | C/T | 0.499965 | 0.00419314 | intron-variant | LNX1 | GRCh38.p7 | 4:53496509 | GGACACAGGATGAGG[C/T]GGGAGAGCAGAGCAG | 84708 |
rs2271560 | snp | C/T | 0.181978 | 0.240568 | intron-variant, downstream-variant-500B | LNX1, FIP1L1 | GRCh38.p7 | 4:53462978 | TGGGAATGTAATGCT[C/T]TGGTATTTACAGAAT | 84708 |
rs2280119 | snp | C/T | 0.359787 | 0.224604 | intron-variant | LNX1 | GRCh38.p7 | 4:53549271 | TCATAGACTTCAATG[C/T]TCAATGTTTTGGACC | 84708 |
rs2280120 | snp | A/G | 0.385359 | 0.210185 | intron-variant | LNX1 | GRCh38.p7 | 4:53549502 | GCAACTAATTGCAAC[A/G]TGTAGATTGTATTTA | 84708 |
rs2280121 | snp | G/T | 0.312837 | 0.241974 | intron-variant | LNX1 | GRCh38.p7 | 4:53549572 | ATTATGGTTGTTTTT[G/T]GTGTGATATTAGTAT | 84708 |
rs2292578 | snp | A/G | 0.186737 | 0.241863 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53498506 | ACTTTCTATCATTTT[A/G]TGACTCTCTGAGATT | 84708 |
rs2292579 | snp | A/G | 0.250732 | 0.249999 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53498350 | CTTCTAGCTTTTTCA[A/G]TCTTCCTCTTCATTC | 84708 |
rs2292580 | snp | A/G | 0.219648 | 0.248151 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53498227 | TTAGAGTAGATTAAT[A/G]GAACATTTTGTATTT | 84708 |
rs2412472 | snp | G/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53531179 | GGGGGAAACCTCTCA[G/T]CTGAGTTTAACTTAC | 84708 |
rs2412483 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510103 | ACACCACTTTTAATT[A/C]CCTTGGGTGCATCTT | 84708 |
rs2412484 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510102 | CACCACTTTTAATTC[C/T]CTTGGGTGCATCTTT | 84708 |
rs2412485 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509167 | TACCCTCCCCACAGT[A/G]GAGTGAGATAGTTAA | 84708 |
rs2412486 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509166 | ACCCTCCCCACAGTA[C/G]AGTGAGATAGTTAAA | 84708 |
rs2412488 | snp | A/G | 0.432651 | 0.170701 | intron-variant | LNX1 | GRCh38.p7 | 4:53464700 | AGAGGATAAGGGATA[A/G]CTAAACCATTTTCTA | 84708 |
rs2412489 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | LNX1 | GRCh38.p7 | 4:53485107 | TGGAAGAGTATTTTG[C/T]AATAGCTGTGTCTTT | 84708 |
rs2412490 | snp | A/G | 0.476746 | 0.10529 | intron-variant | LNX1 | GRCh38.p7 | 4:53606345 | TAGAGGAAATGGCTA[A/G]ATCCCTGGAAACATA | 84708 |
rs2572283 | snp | A/G | 0.267364 | 0.249396 | | | GRCh38.p7 | 4:53615056 | TAATTCATTTGAAGC[A/G]TCATGACAAAACTAG | 84708 |
rs2572284 | snp | A/G | 0.483418 | 0.0895317 | | | GRCh38.p7 | 4:53610640 | GTGAACCCGGGAGGC[A/G]GAGCCTGCAGTGAGC | 84708 |
rs2572285 | snp | G/T | 0.483491 | 0.0893421 | | | GRCh38.p7 | 4:53611077 | TCTATTTTTGCAAAT[G/T]ATATGATTGTAAACC | 84708 |
rs2572286 | snp | G/T | 0.483491 | 0.0893421 | | | GRCh38.p7 | 4:53611488 | GTAATTGGATAAAGT[G/T]ATCTTAAAGTTTCTA | 84708 |
rs2572287 | snp | A/G | 0.477937 | 0.102688 | | | GRCh38.p7 | 4:53617638 | AGAAAAATGTGTAGA[A/G]ACATGCCCACCCACA | 84708 |
rs2572288 | snp | A/G | 0.474 | 0.111014 | | | GRCh38.p7 | 4:53618292 | TGAGCCTTGGGAAAA[A/G]AGTATTCTAAAGAGG | 84708 |
rs2572289 | snp | A/C | 0.437824 | 0.164991 | | | GRCh38.p7 | 4:53626214 | gatagaaaatatgtt[A/C]gttttcaaggactga | 84708 |
rs2572290 | snp | C/T | 0.433673 | 0.1696 | | | GRCh38.p7 | 4:53626864 | AAAAACCACACCATG[C/T]ACCCATCTGTGCCAA | 84708 |
rs2572291 | snp | A/G | 0.312104 | 0.242163 | | | GRCh38.p7 | 4:53627216 | TCTTCCCTAGATTGT[A/G]TGATGGGAACAGAGT | 84708 |
rs2572292 | snp | A/G | 0.322721 | 0.23919 | | | GRCh38.p7 | 4:53629585 | TGCCCAAAGCTGCTC[A/G]AAACCAGTGGCAAAG | 84708 |
rs2572293 | snp | A/T | 0.437965 | 0.164831 | | | GRCh38.p7 | 4:53625413 | ttggattaatatcta[A/T]tcaaatcctttgctt | 84708 |
rs2572294 | snp | G/T | 0.0376037 | 0.131863 | | | GRCh38.p7 | 4:53625285 | tctcacattccatgg[G/T]ttgtctttttatttt | 84708 |
rs2572295 | snp | C/G | 0.447938 | 0.152711 | | | GRCh38.p7 | 4:53625033 | AAGTTTTAAAAATAT[C/G]TATCACAAATATATA | 84708 |
rs2572296 | snp | C/T | 0.438105 | 0.164671 | | | GRCh38.p7 | 4:53624980 | TTATTCTTTACTCTG[C/T]AAAAGAGGATTATTG | 84708 |
rs2572297 | snp | C/T | 0.452473 | 0.146644 | | | GRCh38.p7 | 4:53623949 | CTTATACAGATCTTT[C/T]GATGCAAGTTTGTAT | 84708 |
rs2572298 | snp | C/T | 0 | 0 | | | GRCh38.p7 | 4:53605119 | cgtggtcaaaggagt[C/T]acaaggcccacccag | 84708 |
rs2572299 | snp | G/T | 0.302686 | 0.244385 | | | GRCh38.p7 | 4:53623192 | AGAATTGCTCTCAAC[G/T]CAAACGCTCTCATCC | 84708 |
rs2572300 | snp | C/T | 0.258565 | 0.249853 | | | GRCh38.p7 | 4:53632181 | TGAGGCTGGCCGCTG[C/T]GGTGGCCAGGTCTTT | 84708 |
rs2572301 | snp | A/T | | | | | GRCh38.p7 | 4:53636173 | GAGACTGCACATCTA[A/T]TACTCCttttttttt | 84708 |
rs2572302 | snp | C/T | | | | | GRCh38.p7 | 4:53636180 | CACATCTATTACTCC[C/T]ttttttttttttttt | 84708 |
rs2590768 | snp | A/G | 0.0528381 | 0.153711 | | | GRCh38.p7 | 4:53642051 | CATAGTGGAGAACTC[A/G]TCTCTACAAAAAATA | 84708 |
rs2590769 | snp | C/T | | | | | GRCh38.p7 | 4:53642221 | agagcaaaatcctat[C/T]ttaaaaaaaaaaaaa | 84708 |
rs2590770 | snp | A/G | 0.26308 | 0.250594 | | | GRCh38.p7 | 4:53644875 | GAGAGATGTGGTAAC[A/G]GGGAGGAGGAAGTCT | 84708 |
rs2590771 | snp | C/G | 0.259397 | 0.249823 | | | GRCh38.p7 | 4:53645036 | CAGGAAATCTCCAGA[C/G]AGCCAAAAGATGATC | 84708 |
rs2590772 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 4:53646092 | ATCTGATGCCCAACT[A/G]TACCAGTCATGAAGG | 84708 |
rs2590773 | snp | A/G | 0.259397 | 0.249823 | | | GRCh38.p7 | 4:53646585 | AAATATAGGACCAAC[A/G]TGGCCAGAGTTTCCT | 84708 |
rs2590774 | snp | A/G | | | | | GRCh38.p7 | 4:53628855 | gagttactttactta[A/G]aaaaatggcctcctg | 84708 |
rs2590778 | snp | A/T | 0.259397 | 0.249823 | | | GRCh38.p7 | 4:53649901 | TAGCCAAGCACCTGG[A/T]ACCTCGTAAGCGCTT | 84708 |
rs2590793 | snp | C/T | 0.321053 | 0.23969 | | | GRCh38.p7 | 4:53611956 | TTTCTTCAAATCTAC[C/T]ATGGTCTACTGCATT | 84708 |
rs2590794 | snp | C/T | 0.290718 | 0.246662 | | | GRCh38.p7 | 4:53611739 | TTCATATATTTGTAG[C/T]GTATCCTTGAGTGTG | 84708 |
rs2590795 | snp | G/T | 0.313326 | 0.241847 | | | GRCh38.p7 | 4:53611276 | TGCATTTTCTTTTTT[G/T]GTTATCCTAAGTATT | 84708 |
rs2590796 | snp | A/G | 0.483418 | 0.0895317 | | | GRCh38.p7 | 4:53611038 | CCTCTTTTTTCCCCA[A/G]TGTTTATTCCAGTTT | 84708 |
rs2590797 | snp | A/T | 0.312104 | 0.242163 | | | GRCh38.p7 | 4:53609772 | TAATATATTATATAT[A/T]ATATATAATAGTATA | 84708 |
rs2590798 | snp | G/T | 0.483272 | 0.0899109 | | | GRCh38.p7 | 4:53608788 | AGAACATGATCTCAT[G/T]CTTTTTATGGCTGCA | 84708 |
rs2590799 | snp | G/T | 0.483272 | 0.0899109 | | | GRCh38.p7 | 4:53608134 | CTGTGTAGATGCTCA[G/T]TAGTTTAACTAGGTC | 84708 |
rs2590800 | snp | C/T | 0.483199 | 0.0901004 | | | GRCh38.p7 | 4:53607964 | TTAATTCATCTTGAG[C/T]TGATTTTTGTATATG | 84708 |
rs2590801 | snp | C/T | 0.482979 | 0.0906686 | | | GRCh38.p7 | 4:53607466 | TTTTCCATTTGTTTG[C/T]GTCATCTCTGATTTC | 84708 |
rs2590802 | snp | C/T | 0.483199 | 0.0901004 | | | GRCh38.p7 | 4:53607411 | ATTGTAGAGATTGTT[C/T]CCCTCCCTGGTTAGC | 84708 |
rs2590803 | snp | C/T | 0.483199 | 0.0901004 | | | GRCh38.p7 | 4:53607325 | AATTTGGCTCTCAGC[C/T]TGGATGTCATTGGTG | 84708 |
rs2590804 | snp | C/T | 0.483199 | 0.0901004 | | | GRCh38.p7 | 4:53606941 | agtatgttccttcaa[C/T]gcccagtttgttgag | 84708 |
rs2590816 | snp | A/G | 0.318415 | 0.240457 | | | GRCh38.p7 | 4:53619160 | AAAAAAATTAAGGCC[A/G]TCTAATGTTATTTGG | 84708 |
rs2590817 | snp | C/T | 0.476574 | 0.105661 | | | GRCh38.p7 | 4:53618916 | AAAATAAAAAATATG[C/T]ATACATATAAAAAAA | 84708 |
rs2590818 | snp | A/G | 0.47666 | 0.105476 | | | GRCh38.p7 | 4:53618895 | TATAAAAAAAACAAA[A/G]GGAGCTGTGCTGTGC | 84708 |
rs2590819 | snp | C/T | 0.471483 | 0.115954 | | | GRCh38.p7 | 4:53618289 | CTTTAGAATACTCTT[C/T]TCCCAAGGCTCAAGT | 84708 |
rs2590820 | snp | A/G | 0.475525 | 0.107882 | | | GRCh38.p7 | 4:53615347 | CCCCAAAGCCAGCCC[A/G]GGTAGATTCACGGGA | 84708 |
rs2590821 | snp | A/T | 0.478768 | 0.100824 | | | GRCh38.p7 | 4:53614449 | TGGGGGTCACTTCAC[A/T]AAAGGAAGTATGGAT | 84708 |
rs2590824 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 4:53635986 | ttagcaaaggggcca[A/G]aagtggagcctaATG | 84708 |
rs2590825 | snp | C/T | 0.45198 | 0.147323 | | | GRCh38.p7 | 4:53623555 | GTGAAGAACTTATGG[C/T]TTGCATCAGAATTGT | 84708 |
rs2590826 | snp | C/T | 0.437965 | 0.164831 | | | GRCh38.p7 | 4:53622785 | TGGGTCAGCCTCCCT[C/T]TCTTATTCTCATCTT | 84708 |
rs2616387 | snp | C/T | 0.326506 | 0.238006 | intron-variant | LNX1 | GRCh38.p7 | 4:53650752 | CATGAGGGTGGAATC[C/T]TTTAAGTCTGTGTGA | 84708 |
rs2616388 | snp | C/T | 0.326506 | 0.238006 | intron-variant | LNX1 | GRCh38.p7 | 4:53650502 | AGTTTTCTCCCTTTC[C/T]ACATTTGTAACTCCC | 84708 |
rs2616389 | snp | C/T | 0.309648 | 0.24278 | intron-variant | LNX1 | GRCh38.p7 | 4:53645079 | CTTTTTTGGCGTGGA[C/T]ACTGCCTGGCTGTGC | 84708 |
rs2616392 | snp | C/T | 0.477004 | 0.104734 | intron-variant | LNX1 | GRCh38.p7 | 4:53606518 | AAGACAGATTCACAG[C/T]CAAATTCTACTGGAT | 84708 |
rs2616396 | snp | A/T | 0.483199 | 0.0901004 | intron-variant | LNX1 | GRCh38.p7 | 4:53607132 | GCAAGAGAAAGAAAG[A/T]AAGGAAAGGCATCCA | 84708 |
rs2616400 | snp | C/T | 0.47726 | 0.104176 | intron-variant | LNX1 | GRCh38.p7 | 4:53607911 | GGATAACTGGCTAGC[C/T]AGATGCGGAAGATTG | 84708 |
rs2616401 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | LNX1 | GRCh38.p7 | 4:53608018 | CTTTAAAAACCCTGG[A/G]AGAAAACCTAGGAAA | 84708 |
rs2616404 | snp | A/G | 0.483345 | 0.0897213 | intron-variant | LNX1 | GRCh38.p7 | 4:53608077 | GATTTCATTAAGAAG[A/G]TGCCATAAGCAATTG | 84708 |
rs2616409 | snp | G/T | 0.324145 | 0.238752 | intron-variant | LNX1 | GRCh38.p7 | 4:53608609 | CAACAATCCCATTTT[G/T]GGGTATATACCAGAA | 84708 |
rs2616410 | snp | G/T | 0.39979 | 0.200158 | nc-transcript-variant, intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53605300 | TTTTAGTGTGTTATC[G/T]TCTTTAAACATTGTA | 84708 |
rs2616415 | snp | C/T | 0.478932 | 0.10045 | intron-variant | LNX1 | GRCh38.p7 | 4:53614961 | CAAATTTCGGAATAG[C/T]TCCAAAAGTCAACTT | 84708 |
rs2616416 | snp | A/G | 0.478768 | 0.100824 | intron-variant | LNX1 | GRCh38.p7 | 4:53614542 | CCTTCTGGCTTTTCT[A/G]GTGTGGGTGCAGAGG | 84708 |
rs2616417 | snp | A/G | 0.402806 | 0.197864 | intron-variant | LNX1 | GRCh38.p7 | 4:53621998 | ACAATTCTCATATAC[A/G]TTGGTGCAGAGGCCC | 84708 |
rs2616418 | snp | A/G | 0.451732 | 0.147663 | intron-variant | LNX1 | GRCh38.p7 | 4:53624320 | AATTGGATCATGGGG[A/G]CAATTTCCCCCATAC | 84708 |
rs2616419 | snp | G/T | 0.451359 | 0.148171 | intron-variant | LNX1 | GRCh38.p7 | 4:53624917 | TCATACATTTTAAAA[G/T]AATTCATTAGAAAAT | 84708 |
rs2616420 | snp | C/G | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53625843 | cccagcaattccacc[C/G]cgtgtgtgtgtgtgt | 84708 |
rs2616421 | snp | C/T | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53625844 | ccagcaattccaccc[C/T]gtgtgtgtgtgtgtg | 84708 |
rs2616422 | snp | C/T | 0.438105 | 0.164671 | intron-variant | LNX1 | GRCh38.p7 | 4:53627768 | TCAGCACCTGCTAAC[C/T]CTCTATTGACTTTAC | 84708 |
rs2616423 | snp | C/T | 0.265727 | 0.249505 | intron-variant | LNX1 | GRCh38.p7 | 4:53610645 | CCCGGGAGGCAGAGC[C/T]TGCAGTGAGCCGAGA | 84708 |
rs2616424 | snp | A/G | 0.437824 | 0.164991 | intron-variant | LNX1 | GRCh38.p7 | 4:53629134 | GCTATTGAAATAAAT[A/G]TGAAAAACAGACCAC | 84708 |
rs2616425 | snp | C/G | 0.306927 | 0.243432 | intron-variant | LNX1 | GRCh38.p7 | 4:53631935 | GTTTGAAAATTTTAA[C/G]TAAAATCTGCTGAAG | 84708 |
rs2616435 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53605675 | atataagtgaaatca[C/T]gcagtatttttcttg | 84708 |
rs2668515 | snp | C/T | 0.485049 | 0.0851591 | intron-variant | LNX1 | GRCh38.p7 | 4:53608914 | GCTAAATATTGAGTA[C/T]GTGTGTACACAAAGA | 84708 |
rs2668516 | snp | A/G | 0.31357 | 0.241783 | intron-variant | LNX1 | GRCh38.p7 | 4:53609089 | AGAACAGAATAGAGA[A/G]CCAGAAATAATGCTT | 84708 |
rs2668517 | snp | G/T | 0.483272 | 0.0899109 | intron-variant | LNX1 | GRCh38.p7 | 4:53609169 | GGGGAAAGGACTCCC[G/T]ATGTTTATTACCTGG | 84708 |
rs2668518 | snp | A/G | 0.437965 | 0.164831 | intron-variant | LNX1 | GRCh38.p7 | 4:53627114 | AGCTTGAAATGTTCT[A/G]TGAAAACCCAGTAAG | 84708 |
rs2668519 | snp | A/C | 0.438946 | 0.163706 | intron-variant | LNX1 | GRCh38.p7 | 4:53626348 | ATTGTTTTGTAGTAT[A/C]TTTATTATATGAGGG | 84708 |
rs2668520 | snp | A/G | 0.4661 | 0.125701 | intron-variant | LNX1 | GRCh38.p7 | 4:53625059 | TTAATCTGTATGTAC[A/G]ATGTGCCTACAAGTT | 84708 |
rs2668521 | snp | A/G | 0.312104 | 0.242163 | intron-variant | LNX1 | GRCh38.p7 | 4:53623760 | AGACCTACCTAATCA[A/G]GTTGCTAGTGTGAGG | 84708 |
rs2668522 | snp | C/T | 0.3512 | 0.228601 | intron-variant | LNX1 | GRCh38.p7 | 4:53623530 | AATTGTTCTTGAGTC[C/T]AGGCATGGTGGCTCA | 84708 |
rs2668523 | snp | A/G | 0.308414 | 0.24308 | intron-variant | LNX1 | GRCh38.p7 | 4:53643441 | GGTTTCTTgaccggg[A/G]tggtgtctcagccct | 84708 |
rs2668524 | snp | A/G | 0.273049 | 0.248935 | intron-variant | LNX1 | GRCh38.p7 | 4:53639683 | TCATGAGATATGAAC[A/G]GCTGGTAAGTGGGCG | 84708 |
rs2668525 | snp | C/T | 0.261884 | 0.249717 | intron-variant | LNX1 | GRCh38.p7 | 4:53638589 | AAAAATGAGGAAAAA[C/T]GGGGCACTAAGTAGT | 84708 |
rs2668526 | snp | G/T | 0.307423 | 0.243316 | intron-variant | LNX1 | GRCh38.p7 | 4:53636932 | GGGAGGGAACCTGCG[G/T]TCTGCATACAAGATA | 84708 |
rs2668527 | snp | A/C | 0.258565 | 0.249853 | intron-variant | LNX1 | GRCh38.p7 | 4:53636905 | GATAAGTGTATAACA[A/C]CTTCACTCCAAACAG | 84708 |
rs2668528 | snp | A/G | 0.306679 | 0.24349 | intron-variant | LNX1 | GRCh38.p7 | 4:53636262 | GTTTTGTTTTTGCTC[A/G]ACCGAGGCAAGCATG | 84708 |
rs2668529 | snp | A/G | 0.273856 | 0.248859 | intron-variant | LNX1 | GRCh38.p7 | 4:53631392 | TTTCAGGAATCATTT[A/G]TTTCTTCAGGTCTTC | 84708 |
rs2668541 | snp | C/T | 0.314057 | 0.241654 | intron-variant | LNX1 | GRCh38.p7 | 4:53612491 | TTTATTCAGCTATCC[C/T]CCATTACAGAAAACA | 84708 |
rs2668542 | snp | A/C | 0.479014 | 0.100263 | intron-variant | LNX1 | GRCh38.p7 | 4:53612465 | AAACACTTAGCTTTT[A/C]TAATTTGCAAAAACA | 84708 |
rs2668543 | snp | A/T | 0.479014 | 0.100263 | intron-variant | LNX1 | GRCh38.p7 | 4:53612246 | CTCCCTTACCTACTA[A/T]CCTGCCAGCAATAAG | 84708 |
rs2668544 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | LNX1 | GRCh38.p7 | 4:53611400 | CCACACACATAATCA[A/G]TTTGTAGAATTTAAT | 84708 |
rs2668545 | snp | A/G | 0.483491 | 0.0893421 | intron-variant | LNX1 | GRCh38.p7 | 4:53611201 | CCTTTTCTTATTCCT[A/G]GAGTACAAAAAAGCT | 84708 |
rs2668546 | snp | A/G | 0.265453 | 0.249522 | intron-variant | LNX1 | GRCh38.p7 | 4:53611169 | ATGGTATTTTTGCCT[A/G]TTTGTAGATCCACCT | 84708 |
rs2668549 | snp | A/T | 0.32627 | 0.238082 | intron-variant | LNX1 | GRCh38.p7 | 4:53648186 | atacagctattgtgt[A/T]acatggtatggtggt | 84708 |
rs2668550 | snp | A/G | 0.260227 | 0.249791 | intron-variant | LNX1 | GRCh38.p7 | 4:53646939 | TCCACTTCTAAACAC[A/G]CAGGTTCATTTCAAC | 84708 |
rs2668551 | snp | A/G | 0.309401 | 0.24284 | intron-variant | LNX1 | GRCh38.p7 | 4:53645544 | ACAGTTCTTTGCAAC[A/G]TGCCTCAATGTCTGC | 84708 |
rs2668552 | snp | A/C | 0.308908 | 0.242961 | intron-variant | LNX1 | GRCh38.p7 | 4:53644260 | GAGCATGCCACCATA[A/C]CCATCTAATTTTTGT | 84708 |
rs2668553 | snp | A/C | 0.477768 | 0.103061 | intron-variant | LNX1 | GRCh38.p7 | 4:53618228 | GTATTTCTAGATATC[A/C]GTGAAAGCTGATCAT | 84708 |
rs2668554 | snp | A/G | 0.477515 | 0.103619 | intron-variant | LNX1 | GRCh38.p7 | 4:53616965 | AAAGCTTTGACGATT[A/G]TAGCTTATGGGTGAT | 84708 |
rs2668555 | snp | A/G | 0.47802 | 0.102502 | intron-variant | LNX1 | GRCh38.p7 | 4:53616481 | CATTCATTCTGTGAC[A/G]AATCCAAGTACTAAG | 84708 |
rs2668556 | snp | A/G | 0.477937 | 0.102688 | intron-variant | LNX1 | GRCh38.p7 | 4:53615817 | TGCCTGTATCAAAAC[A/G]TCTCATGTACCCCAT | 84708 |
rs2668557 | snp | C/T | 0.285119 | 0.256277 | intron-variant | LNX1 | GRCh38.p7 | 4:53614821 | AAGGAAATTGCTCCA[C/T]GACCAGGAGGCTGAA | 84708 |
rs2668558 | snp | C/G | 0.327445 | 0.237702 | intron-variant | LNX1 | GRCh38.p7 | 4:53614820 | AGGAAATTGCTCCAT[C/G]ACCAGGAGGCTGAAG | 84708 |
rs2668568 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53605505 | atatttgtaactata[A/G]tctgcatgctgtact | 84708 |
rs2859547 | snp | C/T | 0.479177 | 0.0998894 | intron-variant | LNX1 | GRCh38.p7 | 4:53611642 | TTGCAATTTTAGTGG[C/T]AAAAACCACAATTAC | 84708 |
rs2859819 | snp | C/G | 0.164219 | 0.234823 | intron-variant | LNX1 | GRCh38.p7 | 4:53633769 | TGGCCCAGAAGAGAG[C/G]TGATTGCCACAGTCA | 84708 |
rs2898981 | snp | C/T | 0.319856 | 0.240042 | intron-variant | LNX1 | GRCh38.p7 | 4:53545760 | AGTACAAATCCTGGC[C/T]CATCACTGACTAGCT | 84708 |
rs2898982 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53531040 | gtagctgagaccata[G/T]gcacacaccaccaca | 84708 |
rs3067031 | in-del | -/TATA | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594144 | atatacatatatata[-/TATA]TATTATACACACACT | 84708 |
rs3067033 | in-del | -/CTC | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594030 | TACAGGTTTCTACTT[-/CTC]CTTCTGAATAATGGG | 84708 |
rs3067036 | in-del | -/TG/TTT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53554851 | ttttttttttttttt[-/TG/TTT]gagacagagtctcgc | 84708 |
rs3067038 | in-del | -/AA | 0.345037 | 0.231231 | intron-variant | LNX1 | GRCh38.p7 | 4:53534420 | GGATCTCCTAGGCTC[-/AA]GAGACCCTCCTGCCT | 84708 |
rs3067039 | in-del | -/TT | 0.093417 | 0.194889 | intron-variant | LNX1 | GRCh38.p7 | 4:53526109 | TTTTTAATATTTTTT[-/TT]CTTTTCTAGAAAGTG | 84708 |
rs3067118 | in-del | -/GAA | | | intron-variant | LNX1 | GRCh38.p7 | 4:53464767 | ATGTTCAGGAGAACA[-/GAA]GATTTTAAAGCAATT | 84708 |
rs3113662 | snp | C/T | 0.412416 | 0.190055 | intron-variant | LNX1 | GRCh38.p7 | 4:53621251 | GGAATTGCAGTTCTC[C/T]AAGTCAAATTATATT | 84708 |
rs3210225 | snp | C/G | 0 | 0 | utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53460638 | TCAATCATTTTAGTT[C/G]TTTTAGGGCTTTTTA | 84708 |
rs3215224 | in-del | -/G | 0.217851 | 0.247924 | intron-variant | LNX1 | GRCh38.p7 | 4:53496640 | GAATAAATATGTGGG[-/G]CTTGGGTAAGAACAA | 84708 |
rs3215225 | in-del | -/C | 0.399432 | 0.200425 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53518792 | TTACAGTTGCCCCCC[-/C]AAATAATCAGCCACC | 84708 |
rs3765158 | snp | C/T | 0.419245 | 0.184 | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461417 | AATAATAATGACTAA[C/T]CAAAAATACTTGTAT | 84708 |
rs3811785 | snp | C/T | 0.480951 | 0.0957495 | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461068 | AAACAAAACAAGATA[C/T]GATTAGTATTTTAAT | 84708 |
rs3841111 | in-del | -/ATTTGCCTG | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53508345 | TGAACTTGGAATTTG[-/ATTTGCCTG]CCGCTATATCCTCTC | 84708 |
rs3842589 | in-del | -/T | 0.479583 | 0.0989539 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53508431 | ATTCATAATTTGAGA[-/T]TTTTTTAAAGACGCC | 84708 |
rs3942650 | snp | A/G | 0.496649 | 0.0407971 | intron-variant | LNX1 | GRCh38.p7 | 4:53635264 | TCCTTCTCTCTCCAC[A/G]TCTGGCCTCTGCACT | 84708 |
rs3946758 | snp | A/T | 0.338523 | 0.233803 | intron-variant | LNX1 | GRCh38.p7 | 4:53477740 | TTCTGTATAAGAAAG[A/T]TAAGCAAAAGGGGAC | 84708 |
rs4241974 | snp | A/T | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502425 | CAATAGCATGTTTTT[A/T]AAAATGTACATATCT | 84708 |
rs4241975 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512787 | CAGCTGGGTTTTAGG[C/T]ATTAGCTGCTCTACT | 84708 |
rs4256278 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | LNX1 | GRCh38.p7 | 4:53565018 | acggagtctcgctga[C/T]tgctagcacagcagt | 84708 |
rs4256279 | snp | C/T | 0.499575 | 0.0145705 | intron-variant | LNX1 | GRCh38.p7 | 4:53565080 | tgggggaggggcgcc[C/T]accattgcccaggct | 84708 |
rs4256280 | snp | G/T | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53565115 | taggtaaacaaagca[G/T]cctggaagctcgaac | 84708 |
rs4276343 | snp | A/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53565240 | cctctgcagacttaa[A/G]tgtccctgtctgaca | 84708 |
rs4334807 | snp | A/G | 0.159292 | 0.232964 | intron-variant | LNX1 | GRCh38.p7 | 4:53535477 | AAATCAATCTAACAA[A/G]ACAAATTGGCTCATT | 84708 |
rs4418038 | snp | A/G | 0.421526 | 0.181876 | intron-variant | LNX1 | GRCh38.p7 | 4:53580135 | AAAATAGATGATTCT[A/G]CCTTTGGATAGCTTT | 84708 |
rs4501281 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502999 | gcagtggtgcgatct[C/T]ggctcactgcaagct | 84708 |
rs4864463 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512687 | TGAGAAAGGGAGACA[C/T]TCAGTCCTAATTTAT | 84708 |
rs4864464 | snp | C/T | 0.089084 | 0.191327 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514598 | TCATGGATCTCCAAC[C/T]GGGTCCCTCCCACAA | 84708 |
rs4864465 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514809 | CATCTCTGTACTCAG[A/G]CTTTTCAAGCTAAGG | 84708 |
rs4864466 | snp | A/G | 0.333491 | 0.235646 | intron-variant | LNX1 | GRCh38.p7 | 4:53537809 | GTCACTGACAACAAA[A/G]GAACAGCTTTCAGTG | 84708 |
rs4864467 | snp | C/T | 0.36021 | 0.224397 | intron-variant | LNX1 | GRCh38.p7 | 4:53538203 | TGAAGGATGGGCATG[C/T]GGATTGCTCCTGTGG | 84708 |
rs4864469 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | LNX1 | GRCh38.p7 | 4:53547137 | atgtctattgtgagg[C/T]gcaccattattttta | 84708 |
rs4864470 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | LNX1 | GRCh38.p7 | 4:53554638 | gtgggtggatcacaa[A/G]gtcaggagttcaaga | 84708 |
rs4864471 | snp | G/T | 0.267636 | 0.249377 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53560017 | CTTGGAAGCTTAACA[G/T]CTATCTCCAAGAGGT | 84708 |
rs4864472 | snp | C/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53567822 | aggggatatcaccac[C/T]gatcccacagaaata | 84708 |
rs4864473 | snp | C/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53567915 | aatggataaattcct[C/T]gacacatacactctc | 84708 |
rs4864474 | snp | A/G | 0.410737 | 0.191478 | intron-variant | LNX1 | GRCh38.p7 | 4:53584213 | GGAAGGACAAGATGA[A/G]GAAAGATATTTGAAT | 84708 |
rs4864476 | snp | C/T | 0.47885 | 0.100637 | intron-variant | LNX1 | GRCh38.p7 | 4:53613914 | ggttgaactaattta[C/T]attcccaccaatggg | 84708 |
rs4864478 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | LNX1 | GRCh38.p7 | 4:53620051 | CTGGTCTGTTTGTAA[C/T]GAAACACATTGTGGC | 84708 |
rs4864763 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | LNX1 | GRCh38.p7 | 4:53475179 | CAAAAAGCACCTCAC[A/G]TTGTCCTCTCTTACA | 84708 |
rs4864764 | snp | A/C | 0.0482946 | 0.147699 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53500042 | CAGTGATAGTCAAAC[A/C]CTACAAGTGAGGAGG | 84708 |
rs4864766 | snp | G/T | 0.464629 | 0.128197 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53500804 | TTATATTAAGTAGGC[G/T]ATACCACAGGCAATT | 84708 |
rs4864767 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53500969 | TACAAAAACCACACT[A/G]CCAAACCTAAACCGC | 84708 |
rs4864768 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510339 | TGTTATATGAACATA[C/T]CTCTCATAGTCAGTG | 84708 |
rs4864769 | snp | G/T | 0.089084 | 0.191327 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510542 | GTACCGATTAGCTGC[G/T]TTGGCTTGGAATCAT | 84708 |
rs4864770 | snp | A/G | 0.089084 | 0.191327 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510653 | AACTTGCATTTGAGC[A/G]GCTCCAACGTAACAA | 84708 |
rs4864771 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510661 | TTTGAGCGGCTCCAA[A/C]GTAACAAATACTTGA | 84708 |
rs4864772 | snp | A/T | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512258 | GTAAAATCTCTTGAT[A/T]TTTTAGATGGTAGCA | 84708 |
rs4864773 | snp | A/G | 0.353803 | 0.227431 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512355 | TCTAGCTCCAGAGAT[A/G]GCACATTCTAATCTC | 84708 |
rs4864774 | snp | A/G | 0.489796 | 0.070696 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512508 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGCATGC | 84708 |
rs4864775 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512724 | TTTCTTTCAGGCAGC[A/G]AGAATCAAGATTAGG | 84708 |
rs4864777 | snp | A/G | 0.498547 | 0.0269177 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53516058 | GAGTTAGAGACCCGT[A/G]GCAGGACCCATATTC | 84708 |
rs4864779 | snp | A/G | 0.157311 | 0.232183 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53516907 | GACAACAGAGGGCTC[A/G]CAGTCAGCTCCTTGC | 84708 |
rs4864780 | snp | C/T | 0.496245 | 0.0431677 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53517573 | CTGTAAAGAACTTTC[C/T]GAGTTCAGTTTGGAT | 84708 |
rs4864782 | snp | C/T | 0.108755 | 0.206276 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521931 | cagcctcctgagtag[C/T]taggactacaggtgt | 84708 |
rs4864783 | snp | A/C | 0.0905309 | 0.192535 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521958 | GTGTATACCACCACA[A/C]CTGGCTAACTTTTTC | 84708 |
rs4864784 | snp | C/T | 0.357877 | 0.225527 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53522046 | GCAATCCTTCCATCT[C/T]GATCTCCCAACTAGC | 84708 |
rs4864785 | snp | C/T | 0.316726 | 0.240931 | intron-variant | LNX1 | GRCh38.p7 | 4:53528243 | AAATACATAGTCCTC[C/T]CTTATCCATAGTTTT | 84708 |
rs4864786 | snp | A/C | 0.461148 | 0.133852 | intron-variant | LNX1 | GRCh38.p7 | 4:53532974 | ATCCCGTCAGGGGAG[A/C]CCATATATTGTTTTC | 84708 |
rs4864787 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | LNX1 | GRCh38.p7 | 4:53533113 | GTGTTTATTTGGTTA[A/G]TTAATTGCCTTCTGG | 84708 |
rs4864788 | snp | C/T | 0.136847 | 0.222927 | intron-variant | LNX1 | GRCh38.p7 | 4:53536696 | ATGCTTTAAATGCCT[C/T]TAAAGAGACTTTGAT | 84708 |
rs4864789 | snp | A/T | 0.136847 | 0.222927 | intron-variant | LNX1 | GRCh38.p7 | 4:53536757 | AACCACTCCTTTGTT[A/T]TTCTATAATTAGTTG | 84708 |
rs4864791 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LNX1 | GRCh38.p7 | 4:53543791 | CCTGTCAACCATGCC[A/G]AGAAAGAAGAGAGCA | 84708 |
rs4864792 | snp | A/G | 0.117537 | 0.212022 | intron-variant | LNX1 | GRCh38.p7 | 4:53546869 | GATGTGGTAAAGACC[A/G]AGCCACTTGTGGAGG | 84708 |
rs4864793 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | LNX1 | GRCh38.p7 | 4:53557528 | TAGAGGCAGCAGATC[C/T]ATGCATACAAATTCT | 84708 |
rs4864794 | snp | A/G | 0.267091 | 0.249415 | intron-variant | LNX1 | GRCh38.p7 | 4:53557659 | AAAAAAAAATGCCTT[A/G]TTGAGAAAGTACTGC | 84708 |
rs4864795 | snp | C/T | 0.26326 | 0.249648 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559017 | CCATATTCAAGAAGA[C/T]TAAATTCCATTTTGC | 84708 |
rs4864797 | snp | A/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53568022 | gcttaccaaccaaaa[A/G]gagtccaggaccaga | 84708 |
rs4864798 | snp | A/C | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53568133 | aagagggaatcctcc[A/C]taactcattttatga | 84708 |
rs4864799 | snp | A/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53568156 | ttttatgaggccagc[A/T]tcattctgataccaa | 84708 |
rs4864800 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | LNX1 | GRCh38.p7 | 4:53572866 | AACAAATTGCTTGGA[A/G]GACAAAAGTTTCCTA | 84708 |
rs4864801 | snp | C/T | 0.398354 | 0.201224 | intron-variant, synonymous-codon | LNX1, LOC101928879 | GRCh38.p7 | 4:53576015 | CCTCCATCTTCCCCC[C/T]ACCAGCCTGAAGCCC | 84708 |
rs4864802 | snp | C/T | 0.403684 | 0.197183 | intron-variant | LNX1 | GRCh38.p7 | 4:53584164 | TTTCTGTTGTTGTTG[C/T]TTTTTTTAAAACAGA | 84708 |
rs4864803 | snp | C/T | 0.462472 | 0.13174 | intron-variant | LNX1 | GRCh38.p7 | 4:53613770 | actgcactgaatata[C/T]gggtgtatgtgtctt | 84708 |
rs4864806 | snp | A/G | 0.17332 | 0.23795 | intron-variant | LNX1 | GRCh38.p7 | 4:53634371 | gcctcagtctcccga[A/G]tagctgggactacag | 84708 |
rs4864809 | snp | A/G | 0.499776 | 0.0105807 | intron-variant | LNX1 | GRCh38.p7 | 4:53645746 | CTGAGTTTAGTTTAG[A/G]TGAAGTATGCCACTA | 84708 |
rs5022400 | snp | G/T | 0.46875 | 0.121031 | intron-variant | LNX1 | GRCh38.p7 | 4:53652037 | AGAGAGAGAGAGAGA[G/T]AGAGAGAGAGAGAGA | 84708 |
rs5858213 | in-del | -/ATTA | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53460065 | GAAATAAATTAATTA[-/ATTA]CCCATAGTGTAGTTT | 84708 |
rs5858214 | in-del | -/AGA | 0.306679 | 0.24349 | intron-variant | LNX1 | GRCh38.p7 | 4:53464766 | AATGTTCAGGAGAAC[-/AGA]AGATTTTAAAGCAAT | 84708 |
rs5858215 | in-del | -/A | 0.126564 | 0.217402 | intron-variant | LNX1 | GRCh38.p7 | 4:53490139 | TTGATTCATATAAGG[-/A]AAAAAACAATTACAC | 84708 |
rs5858216 | in-del | -/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53507702 | TGAATACAATACCAC[-/T]TTTCTTGAGCAGCAT | 84708 |
rs5858217 | in-del | -/A | 0.109461 | 0.206758 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53508940 | TGCTATAAAAAAAAA[-/A]TCCAGAAAACTCCAC | 84708 |
rs5858218 | in-del | -/T | 0.126909 | 0.217598 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513105 | TAACCATACCAACAA[-/T]TTTTTTTTTTAACTC | 84708 |
rs5858219 | in-del | -/T | 0.45235 | 0.146814 | intron-variant | LNX1 | GRCh38.p7 | 4:53526450 | TATCAGAATGCCTAC[-/T]TTTTTGGAAGAAATT | 84708 |
rs5858221 | in-del | -/C | 0.0755793 | 0.179102 | intron-variant | LNX1 | GRCh38.p7 | 4:53532892 | TGCTGCCAGCATCAT[-/C]TGTTCCAAATATTTC | 84708 |
rs5858222 | in-del | -/ATTTT | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53535548 | AGATTTTATCATTCT[-/ATTTT]GTTAGTGAATACTTT | 84708 |
rs5858223 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53543909 | AAAACAAAAACAAAC[-/A]AAAAAACAAAACAAT | 84708 |
rs5858225 | in-del | -/AGG | 0.400682 | 0.199487 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594028 | TACCCATTATTCAGA[-/AGG]AGAAGTAGAAACCTG | 84708 |
rs5858226 | in-del | -/ACCTAGT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53617192 | AAAATAAGACCTAGT[-/ACCTAGT]CTAATAATAATAATT | 84708 |
rs5858228 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53649584 | GCCCTGCACTAGCCA[-/C]CCCTGAGGTAGCTCC | 84708 |
rs6148435 | in-del | -/AAGAACTAT/AAGAACTATAAAAACTACGCATTGTTCATTT | 0.432797 | 0.170544 | intron-variant | LNX1 | GRCh38.p7 | 4:53464488 | ATAATCAACATGAAA[lengthTooLong]AAGATGTTTATGGGA | 84708 |
rs6148436 | snp | A/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53529136 | ACACACACACACACA[A/C]ACACATGCACACACA | 84708 |
rs6148437 | in-del | -/AGTAGGGAGAGT | 0.429238 | 0.174281 | intron-variant | LNX1 | GRCh38.p7 | 4:53582096 | AATTTTAGAAACCTA[-/AGTAGGGAGAGT]AAGAATATCAAAACT | 84708 |
rs6148438 | in-del | -/TAGGGAGAGTAG | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53582098 | TTTTAGAAACCTAAG[-/TAGGGAGAGTAG]AATATCAAAACTGTG | 84708 |
rs6554108 | snp | A/G | 0.338976 | 0.23363 | intron-variant | LNX1 | GRCh38.p7 | 4:53474555 | CACCTTTATTGAATG[A/G]ATCTGAAGGGAGGGA | 84708 |
rs6554109 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | LNX1 | GRCh38.p7 | 4:53485868 | TTTATTTCACACCTA[C/T]GTGATATGTACCAAG | 84708 |
rs6554110 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | LNX1 | GRCh38.p7 | 4:53547434 | AGTAACCTGCCCAAG[G/T]TTGCCCAGCTAGAGG | 84708 |
rs6554111 | snp | A/G | 0.440746 | 0.161604 | intron-variant | LNX1 | GRCh38.p7 | 4:53552401 | CTAAAAGTTTTTAAA[A/G]TGGGAAGGAGATGAA | 84708 |
rs6554112 | snp | A/G | 0.441158 | 0.161117 | intron-variant | LNX1 | GRCh38.p7 | 4:53552468 | TGGTGTGTGGAGAAC[A/G]AAATGCACCACCAGT | 84708 |
rs6554113 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | LNX1 | GRCh38.p7 | 4:53560783 | CTGGGCTTCCTACCC[C/T]TAGACTTTGTATTAC | 84708 |
rs6554114 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LNX1 | GRCh38.p7 | 4:53560841 | TAAACCAATATAACA[C/T]AATTTTCCATTACCT | 84708 |
rs6554120 | snp | A/C | 0.489201 | 0.0726845 | intron-variant | LNX1 | GRCh38.p7 | 4:53637955 | GCAAGAGAGAAGGCT[A/C]CCACTGTGTATTCTT | 84708 |
rs6554121 | snp | A/C | 0.486398 | 0.0813386 | intron-variant | LNX1 | GRCh38.p7 | 4:53642849 | CAGATCCCTCCCAGC[A/C]ATGGCATGGAAGCTC | 84708 |
rs6810557 | snp | A/G | 0.481242 | 0.0950111 | intron-variant | LNX1 | GRCh38.p7 | 4:53485520 | GGTATTAAGTTGTTG[A/G]CAGGAATAACACTAC | 84708 |
rs6812114 | snp | C/T | 0.370162 | 0.219229 | intron-variant | LNX1 | GRCh38.p7 | 4:53529910 | GACATGTACAGAGAA[C/T]ACATTAACATGGGGC | 84708 |
rs6812927 | snp | A/G | 0.38934 | 0.207568 | intron-variant | LNX1 | GRCh38.p7 | 4:53547862 | GATGATGACTGTAAG[A/G]CTGATGAATATGGTT | 84708 |
rs6813835 | snp | A/T | 0.251296 | 0.249997 | intron-variant | LNX1 | GRCh38.p7 | 4:53650562 | GAATTTATGGTTTTC[A/T]ATACATATAGATTAA | 84708 |
rs6815418 | snp | C/T | 0.38555 | 0.210062 | intron-variant | LNX1 | GRCh38.p7 | 4:53550329 | GTTCCTGTTGGAATA[C/T]GATTTCTCCAACATA | 84708 |
rs6816209 | snp | A/G | 0.499759 | 0.0109798 | intron-variant | LNX1 | GRCh38.p7 | 4:53644707 | TGGGTAGGTTACCCC[A/G]GCACCAGCAGGGCCT | 84708 |
rs6817878 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LNX1 | GRCh38.p7 | 4:53530413 | AAGAAAATTGTTTAT[C/T]CTCATTTATAATTAA | 84708 |
rs6818788 | snp | C/T | 0.497984 | 0.0316851 | intron-variant | LNX1 | GRCh38.p7 | 4:53490006 | TTTTTGCAGGTATGG[C/T]AATGCAAATAGTCCA | 84708 |
rs6818959 | snp | C/G | 0.499722 | 0.0117779 | intron-variant | LNX1 | GRCh38.p7 | 4:53643592 | GTAACAAAATTCAGG[C/G]GACTGAAGAACTAGC | 84708 |
rs6819831 | snp | C/T | 0.108402 | 0.206034 | intron-variant | LNX1 | GRCh38.p7 | 4:53651248 | ATCCAAGTCCACACT[C/T]TATGTTGAGCTCGTT | 84708 |
rs6820391 | snp | A/C | 0.35894 | 0.225016 | intron-variant | LNX1 | GRCh38.p7 | 4:53548529 | TGTGGAGATATTTCT[A/C]CAGTCTCTTAAAGTT | 84708 |
rs6820658 | snp | A/G | 0.19646 | 0.2442 | intron-variant | LNX1 | GRCh38.p7 | 4:53478406 | GTGGAACCTGGTCTA[A/G]TATCTATACTCAAAC | 84708 |
rs6822201 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | LNX1 | GRCh38.p7 | 4:53493576 | GGACAGTGCAGAGAG[C/T]TGCCAGCACCTACCT | 84708 |
rs6822208 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | LNX1 | GRCh38.p7 | 4:53527440 | CATGAATTCCCCCAC[A/G]CCCATAATTAGTCTC | 84708 |
rs6823039 | snp | C/T | 0.499104 | 0.0211472 | intron-variant | LNX1 | GRCh38.p7 | 4:53544487 | ATGTGAGCCACCATG[C/T]CCGGCCTGAGAGGTG | 84708 |
rs6824775 | snp | G/T | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509319 | ACTCAAAACCCTATA[G/T]GATTGAGCTATTTTA | 84708 |
rs6825364 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | LNX1 | GRCh38.p7 | 4:53474714 | GTCTATGCCGGGATA[C/T]CATGCTTCCTTACCA | 84708 |
rs6826933 | snp | C/T | 0.391954 | 0.205789 | intron-variant | LNX1 | GRCh38.p7 | 4:53579548 | GAACTTCCTGGATGA[C/T]AATAAAGACACATAC | 84708 |
rs6827976 | snp | A/G | 0.340559 | 0.233022 | intron-variant | LNX1 | GRCh38.p7 | 4:53537418 | CATGGATGGAGAAGG[A/G]AGGAAGGCTGTGGGT | 84708 |
rs6831173 | snp | A/C | 0.249038 | 0.249998 | intron-variant | LNX1 | GRCh38.p7 | 4:53524984 | GAGGGAGTCTTAGAG[A/C]GTAAAGATGGGGATT | 84708 |
rs6831363 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | LNX1 | GRCh38.p7 | 4:53580017 | GTCACATGGCGGTGT[A/G]TCCTGCATTGGCACT | 84708 |
rs6832626 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | LNX1 | GRCh38.p7 | 4:53495628 | GCTCACTGCAACCTC[C/T]GCCTCCCAGTTTCAA | 84708 |
rs6834099 | snp | A/G | 0.43978 | 0.162738 | intron-variant | LNX1 | GRCh38.p7 | 4:53480264 | AATAATTACAATTCC[A/G]ACTAAGTCAGTTTGC | 84708 |
rs6834288 | snp | A/G | 0.49334 | 0.057322 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53504510 | ctccatatcagcaat[A/G]aggctgtttcgcttt | 84708 |
rs6835629 | snp | C/T | 0.453697 | 0.14494 | intron-variant | LNX1 | GRCh38.p7 | 4:53480316 | TATGACAGAGGGTTG[C/T]AGCAGAAATGTGACC | 84708 |
rs6836604 | snp | A/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53556081 | aacaagggtcttgta[A/G]atgcaattaaggatc | 84708 |
rs6836800 | snp | A/G | 0.494585 | 0.051751 | intron-variant | LNX1 | GRCh38.p7 | 4:53495983 | TTCTTGCTCATGTCC[A/G]GGGTTTCTGACTGGG | 84708 |
rs6837934 | snp | A/T | 0.445064 | 0.156365 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510988 | GAAACCATTGCACTT[A/T]CAAATTCTTGGGGTT | 84708 |
rs6838260 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | LNX1 | GRCh38.p7 | 4:53489657 | GTAGCTGCACATAAT[A/G]TTCACTCATGAAATT | 84708 |
rs6839922 | snp | C/G | 0.499464 | 0.016365 | intron-variant | LNX1 | GRCh38.p7 | 4:53493301 | TCTGGTTTTGTTCCC[C/G]ACCTGCTCTACTTGG | 84708 |
rs6840343 | snp | C/T | 0.499984 | 0.00279548 | intron-variant | LNX1 | GRCh38.p7 | 4:53493513 | CAATGACAGTAATAC[C/T]ATCCAACACTTGGTC | 84708 |
rs6840442 | snp | A/G | 0.382279 | 0.212137 | intron-variant | LNX1 | GRCh38.p7 | 4:53542495 | AGTGTCCTAACAATC[A/G]CCATCACATTGATCT | 84708 |
rs6840530 | snp | C/T | 0.499989 | 0.00239614 | intron-variant | LNX1 | GRCh38.p7 | 4:53493559 | GGATAAGCTACTGTA[C/T]AGGACAGTGCAGAGA | 84708 |
rs6841529 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509247 | TCACGAGCCCCTTTA[A/G]GAAGTGTCCATTTGC | 84708 |
rs6841853 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LNX1 | GRCh38.p7 | 4:53474450 | tgccacagagactgc[A/G]tggccctcaaagcct | 84708 |
rs6843031 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | LNX1 | GRCh38.p7 | 4:53590694 | AAGTCACATTCTTGC[A/G]GCAATGAGGGAATTA | 84708 |
rs6843281 | snp | C/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53587095 | CTCAGTATCCCAAAA[C/G]GCAACCTACTACATT | 84708 |
rs6843291 | snp | A/G | 0.251014 | 0.249998 | intron-variant | LNX1 | GRCh38.p7 | 4:53652055 | AGAGAGAGAGAGAGA[A/G]AGAGAGACAGAGAAA | 84708 |
rs6843484 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LNX1 | GRCh38.p7 | 4:53652156 | CCTGGTGGAGGAACC[A/G]GGCCATCTTACCTTT | 84708 |
rs6843529 | snp | C/T | 0.498034 | 0.0312882 | intron-variant | LNX1 | GRCh38.p7 | 4:53489687 | TCTAAGTTGAAAAGC[C/T]GTACAGTTTACCAAG | 84708 |
rs6843631 | snp | A/G | 0.040671 | 0.13668 | intron-variant | LNX1 | GRCh38.p7 | 4:53530788 | TATAATTTTTGTTTA[A/G]GTATTTCAGGGTCAA | 84708 |
rs6844977 | snp | C/T | 0.304688 | 0.243945 | intron-variant | LNX1 | GRCh38.p7 | 4:53557056 | CTTTTCATATGATTG[C/T]TAGAAGTCATTCACA | 84708 |
rs6850277 | snp | A/G | 0.469445 | 0.119766 | intron-variant | LNX1 | GRCh38.p7 | 4:53561758 | TTTCATTCACAGCTC[A/G]TTTCAAATTATTGAA | 84708 |
rs6851386 | snp | C/G | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510894 | TCCTAGTAAAAGAAA[C/G]TGGCACCTTTCTCTG | 84708 |
rs6852422 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | LNX1 | GRCh38.p7 | 4:53488070 | GTCACAGACACACAA[A/G]AAATGTCAGACATCA | 84708 |
rs6853185 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | LNX1 | GRCh38.p7 | 4:53546243 | GGAAGAGCATATTCA[A/G]ACATAAAGCCTTATT | 84708 |
rs6853336 | snp | A/G | 0.461037 | 0.134028 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53516157 | GGAGGCAGGAGGACT[A/G]CTTGAGCCCAGAAGT | 84708 |
rs6853466 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513792 | tccatacttgtgttg[C/T]ctgcccatctattct | 84708 |
rs6853943 | snp | A/G | 0.332568 | 0.235971 | intron-variant | LNX1 | GRCh38.p7 | 4:53537058 | CATGCCATTAGGTGA[A/G]AAGACTCACCTCTAG | 84708 |
rs6854868 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LNX1 | GRCh38.p7 | 4:53561521 | TTGAGCCACTGTGCC[C/T]GGCCCTCCGTGTATT | 84708 |
rs6855607 | snp | G/T | 0.182614 | 0.240747 | intron-variant | LNX1 | GRCh38.p7 | 4:53476491 | TGAACAACCTACACA[G/T]CTGTACATGGCAGTC | 84708 |
rs6856301 | snp | C/T | 0.195837 | 0.244062 | intron-variant | LNX1 | GRCh38.p7 | 4:53476133 | GAATCCCCGTCTCTA[C/T]TAGAAATACAAAAAT | 84708 |
rs6856534 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511140 | AAGTATTCAGACTCA[C/T]GTGCTTTGTGTAATA | 84708 |
rs6858782 | snp | C/G | 0.490343 | 0.0688145 | intron-variant | LNX1 | GRCh38.p7 | 4:53647652 | cttaacaatttttaa[C/G]agtacagttcagtag | 84708 |
rs7436831 | snp | C/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53619358 | ccattccctcattcc[C/T]ttcttttcccagccc | 84708 |
rs7437435 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53595432 | ACAGCTTAAGAAAAA[A/G/T]AAACTCAGTATCTTG | 84708 |
rs7655442 | snp | G/T | 0.414905 | 0.187899 | upstream-variant-2KB, intron-variant | LNX1, LNX1-AS2 | GRCh38.p7 | 4:53591998 | AATGACAAATTTAAG[G/T]TGACATTTCCAATTC | 84708 |
rs7658854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LNX1 | GRCh38.p7 | 4:53542486 | GTTTCAAAGAGTGTC[C/T]TAACAATCACCATCA | 84708 |
rs7659449 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53520573 | GTTTTCTGTTATCTG[C/T]CCATGCATTCAAGTG | 84708 |
rs7660884 | snp | C/T | 0.267636 | 0.249377 | intron-variant | LNX1 | GRCh38.p7 | 4:53560441 | CTATCAAATATTTAA[C/T]CTCCCCTTCTTCCTT | 84708 |
rs7660956 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | LNX1 | GRCh38.p7 | 4:53618165 | CCTACCAAATAAATC[C/G]TTATCTTTGGTTTAT | 84708 |
rs7661420 | snp | A/C | 0.475702 | 0.107512 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521816 | GCTTACTCTTTGGTT[A/C]CTGCTCTGCTGGATT | 84708 |
rs7661658 | snp | C/T | 0.268452 | 0.249318 | intron-variant | LNX1 | GRCh38.p7 | 4:53560849 | TATAACACAATTTTC[C/T]ATTACCTGCCATCTG | 84708 |
rs7661802 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53636217 | ttccttttCAGGGGA[A/G]AAGGAGTGGTGGTGA | 84708 |
rs7661823 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53636235 | GGAGTGGTGGTGAAA[A/G]AGGGATGGATGCATG | 84708 |
rs7662597 | snp | C/T | 0.268452 | 0.249318 | intron-variant | LNX1 | GRCh38.p7 | 4:53563162 | AGTGAGCTGAGATCG[C/T]GCCAGCCTGGGCGAC | 84708 |
rs7664897 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53520953 | GGCAATGGTTCGAGA[C/T]TGTCTCAAAAACAAA | 84708 |
rs7665290 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521168 | GAACTGACTGCCTAG[C/T]GAGGTTTTCTGATCA | 84708 |
rs7665900 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | LNX1 | GRCh38.p7 | 4:53649146 | AGTTTCTTTTACAAT[A/G]CCAAAATCTATTTGT | 84708 |
rs7666978 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501645 | agcaacccagccagg[A/G]tcacacagttgataa | 84708 |
rs7668052 | snp | C/T | 0.250732 | 0.249999 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53597217 | TTGGCAAACTATCAA[C/T]TGATATTCCTGATCA | 84708 |
rs7669162 | snp | A/C | 0.394171 | 0.204242 | intron-variant | LNX1 | GRCh38.p7 | 4:53548980 | GTAAGAACTTCTGAA[A/C]ACACAGAAGGAAATG | 84708 |
rs7672484 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502071 | TTCTGTATTGGTCTG[G/T]AAAGAAAATGATTTG | 84708 |
rs7672575 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | LNX1, LOC101928879 | GRCh38.p7 | 4:53575456 | GCTAGGTCATGAGTT[G/T]GATATGCAGACCTTT | 84708 |
rs7672747 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LNX1 | GRCh38.p7 | 4:53625447 | aagtgcacaaagggt[C/T]aataagcacatgaaa | 84708 |
rs7673040 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LNX1 | GRCh38.p7 | 4:53650357 | CAGGGCCTAAGCAGG[G/T]TGCGGAGGGCATCTG | 84708 |
rs7673122 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | LNX1 | GRCh38.p7 | 4:53553071 | ATATGAGGCAAATTC[A/G]TTCAATTTGGTTTAA | 84708 |
rs7675771 | snp | C/G | 0.391954 | 0.205789 | intron-variant | LNX1 | GRCh38.p7 | 4:53580835 | TATTTGTTTGTAAAC[C/G]TTCCTTTACTTTGAT | 84708 |
rs7676184 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53520839 | tggtggtgagtgcct[A/G]taatcccagctactt | 84708 |
rs7679214 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | LNX1, LNX1-AS2 | GRCh38.p7 | 4:53593453 | GGTTTCACTTGCCAT[A/G]TTCACATACACACAG | 84708 |
rs7679302 | snp | C/T | 0.0693013 | 0.172766 | nc-transcript-variant, intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53603555 | gtaaaggatgatgcc[C/T]ggcatctgctcagct | 84708 |
rs7679341 | snp | C/T | 0.221737 | 0.248397 | intron-variant | LNX1 | GRCh38.p7 | 4:53633719 | AGTGTTTGACATGAG[C/T]GCCCTCATCCATCTT | 84708 |
rs7680439 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | LNX1, LNX1-AS2 | GRCh38.p7 | 4:53593433 | GAACAGCCTGGAGAT[C/T]GTGAGGTTTCACTTG | 84708 |
rs7680687 | snp | A/G | 0.324145 | 0.238752 | intron-variant | LNX1 | GRCh38.p7 | 4:53547404 | TTTATAGGTGAGAAA[A/G]GCTCAGAGAAGGTAA | 84708 |
rs7680855 | snp | A/G | 0.391583 | 0.206044 | intron-variant | LNX1 | GRCh38.p7 | 4:53581081 | AGCTCCAGGTGCTCC[A/G]TGTCCCCACCCCACC | 84708 |
rs7681457 | snp | A/G | 0.021333 | 0.101051 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521216 | GGTTTTCAGCTGCCT[A/G]TGATGAGCTCTTTTT | 84708 |
rs7681869 | snp | A/G | 0.389152 | 0.207694 | intron-variant | LNX1 | GRCh38.p7 | 4:53581606 | AACATGGTGGCAGGC[A/G]AGAGAACATGTGCAG | 84708 |
rs7682199 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | LNX1 | GRCh38.p7 | 4:53477196 | GGGGTTTTCTAAAGC[A/G]CAGCTATCGGTGTTT | 84708 |
rs7682325 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | LNX1 | GRCh38.p7 | 4:53565081 | gggggaggggcgcct[A/G]ccattgcccaggctt | 84708 |
rs7682908 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53529142 | acacacacaaacaca[C/T]gcacacacaGAAAAC | 84708 |
rs7683461 | snp | C/T | 0.391583 | 0.206044 | intron-variant | LNX1 | GRCh38.p7 | 4:53581696 | AGCATGGGAAAAACC[C/T]GCCCCCATGATTCAA | 84708 |
rs7685317 | snp | A/G | 0.263535 | 0.249633 | intron-variant | LNX1 | GRCh38.p7 | 4:53560614 | TGTCTCCATTGGCAC[A/G]TTGTATTTTTCCCTG | 84708 |
rs7687290 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | LNX1 | GRCh38.p7 | 4:53497670 | TTGTTATGCAACCCT[C/G]CCAGGCAGCATAGTT | 84708 |
rs7687977 | snp | A/G | 0.0663309 | 0.169604 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53575127 | GCTGGGATTACAGGC[A/G]CGCGCCACCATGCCT | 84708 |
rs7688605 | snp | C/T | 0.484632 | 0.086302 | intron-variant | LNX1 | GRCh38.p7 | 4:53630744 | CAGCTTATGTATTGA[C/T]TGGCTGATAAAAATG | 84708 |
rs7688641 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | LNX1 | GRCh38.p7 | 4:53477922 | AAACTTCACAGTTTA[A/T]CTCTTGAACCTGGAC | 84708 |
rs7688853 | snp | C/T | 0.499693 | 0.0123764 | intron-variant | LNX1 | GRCh38.p7 | 4:53487048 | GTGTTCAGCCTGCAA[C/T]TGACTCTTTCTCTTC | 84708 |
rs7689262 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | LNX1 | GRCh38.p7 | 4:53543409 | CCTGATATGTCATAC[A/G]CATTTGATAAGTATT | 84708 |
rs7690908 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | LNX1 | GRCh38.p7 | 4:53473256 | ACACAAAAGTGGAAG[A/G]GAAAAATAAAAACAC | 84708 |
rs7691696 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | LNX1 | GRCh38.p7 | 4:53490385 | GTCATGATTGGGAAA[C/T]TGACTTGAGAAATTG | 84708 |
rs7691817 | snp | A/G | 0.234982 | 0.249549 | upstream-variant-2KB, intron-variant | LNX1, LNX1-AS2 | GRCh38.p7 | 4:53591694 | TCTTTGTGGACAAAT[A/G]AATCAGTTAGAGCAA | 84708 |
rs7691892 | snp | A/G | 0.499563 | 0.0147699 | intron-variant | LNX1 | GRCh38.p7 | 4:53494214 | AGTCTCACAAGATCC[A/G]ATGGTTTTATAAAGG | 84708 |
rs7695583 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | LNX1 | GRCh38.p7 | 4:53561031 | TCAGATATCACTGAT[C/T]ATCTCCTATTTTCTT | 84708 |
rs7697542 | snp | C/T | 0.382666 | 0.211895 | intron-variant | LNX1 | GRCh38.p7 | 4:53546902 | GAGCTGTGTGGAAGG[C/T]GAGGCCTCAGCCACT | 84708 |
rs7697807 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | LNX1 | GRCh38.p7 | 4:53494730 | CATCTAACCCAGGGG[C/T]ACATAAGCAGCAGAA | 84708 |
rs7698929 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53529143 | cacacacaaacacat[A/G]cacacacaGAAAACA | 84708 |
rs7699951 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599894 | ATATGGTCTCAGTTT[C/T]GTGCCCACAGTCAGG | 84708 |
rs9312642 | snp | A/G | 0.419296 | 0.183954 | intron-variant | LNX1 | GRCh38.p7 | 4:53589884 | AGCTTTGTTCCTTTA[A/G]TACTCAGACATGCTG | 84708 |
rs9312643 | snp | A/T | 0.0807149 | 0.183963 | intron-variant | LNX1 | GRCh38.p7 | 4:53652020 | TTTGATGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 84708 |
rs9654328 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | LNX1 | GRCh38.p7 | 4:53565012 | taccccacggagtct[C/T]gctgattgctagcac | 84708 |
rs9715657 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53652035 | Tgagagagagagaga[G/T]agagagagagagaga | 84708 |
rs9784410 | snp | A/G | 0.461813 | 0.132798 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53601384 | CTGAGTCTGCCCAGG[A/G]GGTGGACAGGAAATG | 84708 |
rs9784552 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53603327 | TTCATTAAATAAACA[C/T]ACAAATGGACAAAAT | 84708 |
rs9992650 | snp | C/T | 0.204803 | 0.245881 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512184 | ACAGTGGCTGCTCCA[C/T]CCTTCCCTGTTAAAA | 84708 |
rs9995952 | snp | A/C | 0.287606 | 0.247155 | intron-variant | LNX1 | GRCh38.p7 | 4:53469642 | aaatagatgcaataa[A/C]aaatgacaaagggga | 84708 |
rs9996049 | snp | C/G | 0.338296 | 0.233889 | intron-variant | LNX1 | GRCh38.p7 | 4:53466009 | tcaaaaaattatttt[C/G]gctttTTGTTTGTAA | 84708 |
rs9996659 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | LNX1 | GRCh38.p7 | 4:53545018 | GGGAGTGGTACCCAG[A/G]TGCTTTTTTCTATTA | 84708 |
rs9996883 | snp | A/G | 0.499354 | 0.0179596 | intron-variant | LNX1 | GRCh38.p7 | 4:53491010 | CCAGTGTTAGGCAAG[A/G]TTTTATTCCATAAAT | 84708 |
rs9997623 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | LNX1 | GRCh38.p7 | 4:53491809 | TTTTTTTGTTTGTTT[G/T]TTTTTTGAGAAAAGT | 84708 |
rs9997844 | snp | A/G | 0.338069 | 0.233974 | intron-variant | LNX1 | GRCh38.p7 | 4:53475258 | CACAAAAAACAAAAT[A/G]ATTTTAATAGATCCT | 84708 |
rs9998954 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | LNX1 | GRCh38.p7 | 4:53470413 | aaactggaagcattc[A/C]ctttgaaaactggca | 84708 |
rs9999406 | snp | C/T | 0.495963 | 0.0447464 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515178 | ATGGCTTCCTCACAT[C/T]AGTGCCAGAGAAGTG | 84708 |
rs10000315 | snp | C/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53570427 | gaacaaaaaaccaaa[C/T]accgcatattctgac | 84708 |
rs10000457 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | LNX1 | GRCh38.p7 | 4:53555372 | TTCTGCCTCATTCCT[C/T]TAAGCACTTCAAGAT | 84708 |
rs10001337 | snp | C/T | 0.203267 | 0.245593 | intron-variant | LNX1 | GRCh38.p7 | 4:53485362 | ATGATCTAAGCACCT[C/T]ATAAGAACTGAGAAA | 84708 |
rs10002285 | snp | C/T | 0.106633 | 0.204807 | intron-variant, synonymous-codon | LNX1, LOC101928879 | GRCh38.p7 | 4:53576165 | GGCCTGGCTGCCCCA[C/T]GTTGCTGACTTTCAG | 84708 |
rs10003158 | snp | C/G | 0.496382 | 0.0423778 | intron-variant | LNX1 | GRCh38.p7 | 4:53468850 | taaagcaagtcctta[C/G]tgacctacaaagaga | 84708 |
rs10005424 | snp | A/G | 0.497749 | 0.0334707 | intron-variant | LNX1 | GRCh38.p7 | 4:53474830 | GGAGTGCAGTGGCGC[A/G]ATCTCAGCTCACTGC | 84708 |
rs10005578 | snp | C/T | 0.498503 | 0.0273153 | intron-variant | LNX1 | GRCh38.p7 | 4:53627063 | CTTCTGCAGGAGTTC[C/T]TCTTGTCCTCTGCAG | 84708 |
rs10005885 | snp | C/T | 0.433673 | 0.1696 | intron-variant | LNX1 | GRCh38.p7 | 4:53627394 | GTTGGTAAACTGATT[C/T]TAACAGGGTTGAGCA | 84708 |
rs10006267 | snp | C/T | 0.49533 | 0.0480965 | intron-variant | LNX1 | GRCh38.p7 | 4:53627797 | ACTGCTCCTAAAAGA[C/T]GGTCTAGAAGTGCTT | 84708 |
rs10006662 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512157 | GTGAGCAGTGCTGCT[C/T]GACTTAAGGACACAG | 84708 |
rs10007397 | snp | A/C | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53573407 | tttatgttacatttt[A/C]ttagaattttaaaaa | 84708 |
rs10007903 | snp | A/G | 0.497855 | 0.0326773 | intron-variant | LNX1 | GRCh38.p7 | 4:53475146 | GGAAGAAAGACATTC[A/G]CTTGGTTGTATTTGG | 84708 |
rs10008212 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53570525 | gttgtggggtggggg[A/G]aggggggagggatag | 84708 |
rs10008334 | snp | A/C | 0.450483 | 0.149354 | intron-variant | LNX1 | GRCh38.p7 | 4:53482051 | CCTTTATCCTTAAAC[A/C]AGGTAGTAAATGTTG | 84708 |
rs10009930 | snp | C/T | 0.3748 | 0.216622 | intron-variant | LNX1 | GRCh38.p7 | 4:53588397 | GATAACCCTATTACA[C/T]AGCTGATGAGAGCAG | 84708 |
rs10010205 | snp | C/G | 0.495368 | 0.0478996 | intron-variant | LNX1 | GRCh38.p7 | 4:53623570 | ACCATAAGTTCTTCA[C/G]AGATTTTTGTTAAGA | 84708 |
rs10011394 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | LNX1 | GRCh38.p7 | 4:53488900 | GGTTTGGAAACAGAA[C/T]CCTTCCCCTTCCCTT | 84708 |
rs10016844 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | LNX1 | GRCh38.p7 | 4:53560896 | tacaATCCCTTGGGG[C/T]TAAAACCCAACCTCA | 84708 |
rs10016971 | snp | C/G | 0.392511 | 0.205404 | intron-variant | LNX1 | GRCh38.p7 | 4:53578625 | CCTTGATTTCACTGA[C/G]TGCTGAGGCAGAATG | 84708 |
rs10017896 | snp | A/T | 0.18325 | 0.240924 | intron-variant | LNX1 | GRCh38.p7 | 4:53652022 | TGATGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 84708 |
rs10019672 | snp | C/T | 0.212425 | 0.24716 | intron-variant | LNX1 | GRCh38.p7 | 4:53466519 | gcagcacaccgagca[C/T]gagccaaagcagggc | 84708 |
rs10021678 | snp | A/G | 0.49706 | 0.0382258 | intron-variant | LNX1 | GRCh38.p7 | 4:53623561 | CTGATGCAAACCATA[A/G]GTTCTTCACAGATTT | 84708 |
rs10021772 | snp | C/T | 0.480384 | 0.0970728 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53507297 | CCATGTCCATCCAGC[C/T]TTATGGGGAGTTCAT | 84708 |
rs10021838 | snp | C/T | 0.430285 | 0.173197 | intron-variant | LNX1 | GRCh38.p7 | 4:53582666 | ATATCAGATTATTTC[C/T]GAGGTTACTTTTAGC | 84708 |
rs10022794 | snp | A/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53488782 | CCATACAGACCTTAC[A/C]TGACAATACAGACAA | 84708 |
rs10024066 | snp | C/T | 0.108402 | 0.206034 | upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53653740 | GAAACTTCTGCCTGG[C/T]GAGATGAAGTCAGCA | 84708 |
rs10024162 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | LNX1 | GRCh38.p7 | 4:53534821 | TTTCTATTCAGCCAT[A/G]TACATTGTCCAGACT | 84708 |
rs10026005 | snp | A/C | 0.33875 | 0.233717 | intron-variant | LNX1 | GRCh38.p7 | 4:53468497 | acacataacaatatt[A/C]accttaaatgtaaat | 84708 |
rs10027185 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | LNX1 | GRCh38.p7 | 4:53639497 | TAAAaatgttaatat[C/T]ccagaaaaaataagg | 84708 |
rs10027377 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | LNX1 | GRCh38.p7 | 4:53639737 | AGTCAGAGGCATAAT[C/G]AAGAGTTATTTAggt | 84708 |
rs10027453 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | LNX1 | GRCh38.p7 | 4:53639802 | tttgggaggccgagg[C/T]gggtggatcacttga | 84708 |
rs10027544 | snp | A/C | 0.488905 | 0.0736498 | intron-variant | LNX1 | GRCh38.p7 | 4:53639920 | TGCCTATAATCCCAG[A/C]TACTTGGGAGGCTGA | 84708 |
rs10028142 | snp | A/G | 0.496382 | 0.0423778 | intron-variant | LNX1 | GRCh38.p7 | 4:53465700 | ACATGTTTAAATTGT[A/G]CATACACTAAAAAGA | 84708 |
rs10028214 | snp | A/G | 0.337614 | 0.234145 | intron-variant | LNX1 | GRCh38.p7 | 4:53465756 | GAAAAATATGTTGCT[A/G]GCTTTTTTTGAAGTT | 84708 |
rs10031491 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53558270 | CCTCCTGCAGGATGC[A/G]GACTGGTTCTTGGGA | 84708 |
rs10031525 | snp | G/T | 0.49614 | 0.0437598 | upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53653412 | TAATTAGTGAATTAA[G/T]TAGTCTCTTTCCAGA | 84708 |
rs10031866 | snp | G/T | 0.496905 | 0.0392151 | intron-variant | LNX1 | GRCh38.p7 | 4:53623671 | ATTTGAAGTTATATG[G/T]CTATGTTTTATTTTT | 84708 |
rs10032903 | snp | G/T | 0.499703 | 0.0121769 | intron-variant | LNX1 | GRCh38.p7 | 4:53488856 | GTCATCAGTCATTCC[G/T]GTTGATATGTCAGTG | 84708 |
rs10033726 | snp | A/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53611849 | GTAGGACAAACCCTC[A/C]CAATAAAAACTGAGA | 84708 |
rs10212730 | snp | A/C | 0.472803 | 0.113397 | intron-variant | LNX1 | GRCh38.p7 | 4:53539657 | ATATTCAGTTGCAGA[A/C]AATGTTTTTGTTCTA | 84708 |
rs10213560 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LNX1 | GRCh38.p7 | 4:53570069 | acactgttggtggga[C/T]tgtaaactagttcaa | 84708 |
rs10213561 | snp | C/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53570106 | tggaagtcagtgtgg[C/T]gattcctcagggatc | 84708 |
rs10517300 | snp | C/T | 0.173965 | 0.238157 | intron-variant | LNX1 | GRCh38.p7 | 4:53529573 | CCACCCAGTAAAACA[C/T]GAAGCTCTGTTGGCA | 84708 |
rs10517301 | snp | C/T | 0.166506 | 0.235645 | intron-variant | LNX1 | GRCh38.p7 | 4:53530757 | CCAAAGACAAGACTA[C/T]GCAGCCAGTTAAAAC | 84708 |
rs10517304 | snp | C/T | 0.235564 | 0.249583 | intron-variant | LNX1 | GRCh38.p7 | 4:53586548 | TAAGTCCACATATTC[C/T]AAGTCACAAATTAGT | 84708 |
rs10517305 | snp | A/G | 0.184521 | 0.241273 | intron-variant | LNX1 | GRCh38.p7 | 4:53590607 | CAGAACAACTTCCTC[A/G]GTATATTTGCTATTA | 84708 |
rs10553873 | in-del | -/AA | 0.363776 | 0.222609 | intron-variant | LNX1 | GRCh38.p7 | 4:53610716 | CCCGTCTCAAAGAGG[-/AA]AAAAAAAAAAAAAAA | 84708 |
rs10641778 | in-del | -/TTC | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53536335 | TCACTCCACATCTTC[-/TTC]AAGAGGGGACTTTTA | 84708 |
rs10658913 | in-del | -/GTCT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53614983 | GAAATTTGTTCATCT[-/GTCT]TTGAACACCGAGAAT | 84708 |
rs10665279 | in-del | -/AC/CA | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514662 | ATTTGGGTGAGGACA[-/AC/CA]GTCAAACCATATCAG | 84708 |
rs10670420 | in-del | -/TT | 0.25801 | 0.249872 | intron-variant | LNX1 | GRCh38.p7 | 4:53463406 | TTTTGAGTATTTAAC[-/TT]TTTATTGCCGCAGCG | 84708 |
rs10683892 | in-del | -/TCTG | 0.31503 | 0.241394 | intron-variant | LNX1 | GRCh38.p7 | 4:53614980 | TCCGAAATTTGTTCA[-/TCTG]ATCTTTGAACACCGA | 84708 |
rs10711730 | snp | A/T | 0.355647 | 0.22658 | intron-variant | LNX1 | GRCh38.p7 | 4:53541746 | CTCAGTCTGAGTCAT[A/T]AAAAAAAAGTAGGCC | 84708 |
rs10719074 | in-del | -/A | 0.0901694 | 0.192235 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512379 | TAATCTCTGGTAATT[-/A]AAAAAAACTGCCAAC | 84708 |
rs10735529 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | LNX1 | GRCh38.p7 | 4:53589314 | CTGCCCACCTTGTTT[A/G]ATGACATTGTTTAAG | 84708 |
rs11133275 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | LNX1 | GRCh38.p7 | 4:53493030 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 84708 |
rs11133276 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502873 | tttatttgctcatcc[A/G]taagaaatgcctcta | 84708 |
rs11133278 | snp | A/G | 0.494815 | 0.0506538 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53575059 | TGATCTCTGCTCACT[A/G]CAACTGCCACCTCCC | 84708 |
rs11133279 | snp | C/T | 0.496279 | 0.0429702 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53575106 | CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA | 84708 |
rs11133280 | snp | A/G | 0.361053 | 0.22398 | intron-variant | LNX1 | GRCh38.p7 | 4:53581076 | CCTGCAGCTCCAGGT[A/G]CTCCGTGTCCCCACC | 84708 |
rs11133282 | snp | A/G | 0.191147 | 0.242974 | nc-transcript-variant, intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53604950 | CACTCCTCACAACCC[A/G]GGTGATTTGCAAAGT | 84708 |
rs11285844 | in-del | -/A | 0.0759472 | 0.179459 | intron-variant | LNX1 | GRCh38.p7 | 4:53466157 | ACTTTTTGTTTTAAG[-/A]AAAAAAAAATCACAT | 84708 |
rs11296034 | in-del | -/C | 0.499477 | 0.0161657 | intron-variant | LNX1 | GRCh38.p7 | 4:53486302 | CAGAGCGCACTACAG[-/C]CCCAGAGCTCCTGAG | 84708 |
rs11301662 | in-del | -/A | 0.381308 | 0.21274 | intron-variant | LNX1 | GRCh38.p7 | 4:53543529 | AGCTTGGAAAAGAAG[-/A]AAAAAAAATCACACT | 84708 |
rs11305648 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53491274 | AGTTTTCAAAGTGAG[-/A]AAAAAAAAAAAAATC | 84708 |
rs11345850 | in-del | -/G | 0.4944 | 0.0526182 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502314 | CCTCTGAGATATTGT[-/G]GGTTTGGTTCCAGAC | 84708 |
rs11375920 | in-del | -/A/AA | 0.487241 | 0.0788465 | intron-variant | LNX1 | GRCh38.p7 | 4:53552828 | GCAAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA | 84708 |
rs11377097 | in-del | -/A/AA | 0.497151 | 0.037632 | intron-variant | LNX1 | GRCh38.p7 | 4:53548121 | TGAAAAAAAAAAAAA[-/A/AA]GTCGGGGGAAATATG | 84708 |
rs11386482 | in-del | -/T | 0.400504 | 0.199621 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521978 | TAACTTTTTCATTAA[-/T]TTTTTTTGTAGAGAC | 84708 |
rs11395102 | in-del | -/T | 0.365646 | 0.221644 | intron-variant | LNX1 | GRCh38.p7 | 4:53474774 | TCTTCTTTTTTTTTT[-/T]GAGACAGAGTCTCTC | 84708 |
rs11401056 | in-del | -/T/TT | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501282 | AGATGATAATAATCT[-/T/TT]TTTTTTTTTTTTTTT | 84708 |
rs11404981 | in-del | -/AA | | | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53576652 | AAATTAAAAAAAAAA[-/AA]GAATCCTGCCTCTTC | 84708 |
rs11415751 | in-del | -/A/AA | | | intron-variant | LNX1 | GRCh38.p7 | 4:53527072 | AAAAAAAAAAAAAAA[-/A/AA]CTAGAAGAACAAAAC | 84708 |
rs11440722 | in-del | -/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53636203 | TTTTTTTTTTTTTTT[-/T]CCTTTTCAGGGGAGA | 84708 |
rs11451720 | in-del | -/T | 0.375 | 0.216506 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53505266 | ACTTTTTTTTTTTTT[-/T]GAGATGGAGTCACCC | 84708 |
rs11451893 | in-del | -/A | 0.446771 | 0.154211 | intron-variant | LNX1 | GRCh38.p7 | 4:53529953 | TGCTACAGAGACTAG[-/A]AAAAAATGTAGGCGA | 84708 |
rs11721994 | snp | C/T | 0.432651 | 0.170701 | intron-variant | LNX1 | GRCh38.p7 | 4:53467809 | aagaataaaaagaaa[C/T]gaacaaagtctccaa | 84708 |
rs11723168 | snp | A/G | 0.460589 | 0.13473 | intron-variant | LNX1 | GRCh38.p7 | 4:53536204 | CAATGCTCTCCATCT[A/G]TGAATACACTTCCCA | 84708 |
rs11723567 | snp | C/T | 0.349233 | 0.229462 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513885 | ttacaacgatctata[C/T]ggccctatattttct | 84708 |
rs11723672 | snp | A/G | 0.219947 | 0.248187 | intron-variant | LNX1 | GRCh38.p7 | 4:53466763 | gcagtaaagtgcaag[A/G]tggcagcaaggctgg | 84708 |
rs11724704 | snp | C/T | 0.317451 | 0.240729 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515470 | CTCCTAGCAAGCTCA[C/T]GAGTTCCCTTTCCAT | 84708 |
rs11726075 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53540957 | gcctggccaacatgg[G/T]gaaaccctgtctctt | 84708 |
rs11726353 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514164 | CCCTGCTTATTTTCT[C/G]TCTATGGAATGCAAG | 84708 |
rs11727318 | snp | A/G | 0.303187 | 0.244277 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53574982 | TCCATTAGATATTTC[A/G]TTTTTTTTTTTTCTT | 84708 |
rs11727886 | snp | A/G | 0.135484 | 0.22223 | intron-variant | LNX1 | GRCh38.p7 | 4:53583972 | AACAACAACAACAAC[A/G]ACGACAAATGAAGGC | 84708 |
rs11728424 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | LNX1 | GRCh38.p7 | 4:53573365 | taccactgaactgta[C/T]actcatagtggttaa | 84708 |
rs11728872 | snp | C/G | 0.283421 | 0.247756 | intron-variant | LNX1 | GRCh38.p7 | 4:53488630 | CATAGGGGATTGTCT[C/G]TATGCTCTATGAATC | 84708 |
rs11731437 | snp | C/T | 0.279461 | 0.248258 | intron-variant | LNX1 | GRCh38.p7 | 4:53586917 | AATCTAAAATAATCC[C/T]ATGAGATCATTAAGG | 84708 |
rs11732409 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53479110 | ttgctttgttgctca[A/G]gctggtctggaactc | 84708 |
rs11733754 | snp | A/G | 0.332799 | 0.23589 | intron-variant | LNX1 | GRCh38.p7 | 4:53534834 | ATATACATTGTCCAG[A/G]CTGCTATGTCTGGGG | 84708 |
rs11734681 | snp | A/G | 0.495891 | 0.0451408 | intron-variant | LNX1 | GRCh38.p7 | 4:53486925 | AAACATAGTCCAGAA[A/G]CCTCATTTATATGTA | 84708 |
rs11736112 | snp | A/C | 0.307671 | 0.243257 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515462 | TCTCCTTTCTCCTAG[A/C]AAGCTCATGAGTTCC | 84708 |
rs11737139 | snp | C/G | 0.495291 | 0.0482933 | intron-variant | LNX1 | GRCh38.p7 | 4:53483170 | TAGTAAGTCTCACGA[C/G]ATCTGATGATTTTAT | 84708 |
rs11843528 | snp | C/G/T | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53470278 | AGAAAAGGCCTTTGA[C/G/T]AAAATTCAACAGCCC | 84708 |
rs11930043 | snp | C/G | 0 | 0 | nc-transcript-variant, intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53605211 | gagcatgtggaatgg[C/G]aattgtgttgtatgg | 84708 |
rs11931649 | snp | C/T | 0.170408 | 0.236992 | intron-variant | LNX1 | GRCh38.p7 | 4:53613697 | ccacattttctttat[C/T]cagtctatgattgat | 84708 |
rs11934069 | snp | C/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53525906 | TGAGGTCAGTCACAT[C/G]TTTAGGAAATACCAT | 84708 |
rs11934631 | snp | A/G | 0.299916 | 0.244966 | intron-variant | LNX1 | GRCh38.p7 | 4:53538930 | GGAACAAGCCAAATG[A/G]CCGATTAACAGTCAT | 84708 |
rs11934906 | snp | A/G | 0.278664 | 0.248351 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53503551 | aggcctcaacagtgg[A/G]cttaaaatattgagt | 84708 |
rs11935144 | snp | C/T | 0.278664 | 0.248351 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511430 | TCCTTTCAGTTACTC[C/T]GAGCACTAAGTACTC | 84708 |
rs11936085 | snp | A/G | 0.496279 | 0.0429702 | intron-variant | LNX1 | GRCh38.p7 | 4:53469472 | aaaagctagcagaag[A/G]caagaaataactaag | 84708 |
rs11936494 | snp | C/G | 0.330482 | 0.236691 | intron-variant | LNX1 | GRCh38.p7 | 4:53545163 | ACTAATCACTTTAAA[C/G]AATGACTTTGAGAAC | 84708 |
rs11936500 | snp | A/C | 0.229136 | 0.249128 | intron-variant | LNX1 | GRCh38.p7 | 4:53587843 | CAGAAGCCCACTCCC[A/C]ACAGGTTTATGAAAG | 84708 |
rs11938583 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599380 | ggtttataaatgcca[C/T]ggcaacatcaggaag | 84708 |
rs11939219 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | LNX1 | GRCh38.p7 | 4:53547670 | ATTCTTGGCTCATGG[A/G]GCAACCAGGAAGACA | 84708 |
rs11941712 | snp | C/T | 0.415235 | 0.18761 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53597657 | TCTCTCCAGGGCAGA[C/T]TTCTGTCTAGGAGGC | 84708 |
rs11942048 | snp | A/T | 0.228842 | 0.249103 | intron-variant | LNX1 | GRCh38.p7 | 4:53588009 | CGTACTACCGTTTCC[A/T]TCATTATTACATCCA | 84708 |
rs11944047 | snp | A/T | 0.45574 | 0.142025 | intron-variant | LNX1 | GRCh38.p7 | 4:53483484 | CAGAGCTGCAGGTCA[A/T]TCAGACTAAATCTTA | 84708 |
rs11944299 | snp | C/T | 0.451856 | 0.147493 | intron-variant | LNX1 | GRCh38.p7 | 4:53493055 | GCTCACTGAAACCTC[C/T]GCCTCCCGAGTTCAA | 84708 |
rs11945338 | snp | A/G | 0.231189 | 0.249291 | intron-variant | LNX1 | GRCh38.p7 | 4:53587811 | GCTCCAGGAAGACCC[A/G]CTGTTTACTCACATC | 84708 |
rs11945428 | snp | G/T | 0.338523 | 0.233803 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599983 | AGTAACATCTGTAGC[G/T]GTTTAGATGAATTTA | 84708 |
rs12186283 | snp | A/G | 0.399968 | 0.200024 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53596739 | GACTTCATCCTGAAG[A/G]CTTCCACATTCTTGT | 84708 |
rs12331079 | snp | A/C | 0.449218 | 0.151037 | intron-variant | LNX1 | GRCh38.p7 | 4:53543394 | ACAGCCTAGAACATG[A/C]CTGATATGTCATACA | 84708 |
rs12499401 | snp | C/T | 0.338296 | 0.233889 | intron-variant | LNX1 | GRCh38.p7 | 4:53472927 | GTAAGAAGAGAATAA[C/T]TGAGTTTGCTAGTTT | 84708 |
rs12501431 | snp | G/T | 0.25214 | 0.249991 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510053 | aattctgtgttttct[G/T]gcaaagggacaagca | 84708 |
rs12503229 | snp | A/C | 0.233818 | 0.249476 | intron-variant | LNX1 | GRCh38.p7 | 4:53472688 | CAACAACAACAACAA[A/C]AAAAAAAAAAACAAA | 84708 |
rs12505040 | snp | C/T | 0.181022 | 0.240296 | intron-variant | LNX1 | GRCh38.p7 | 4:53473311 | GGAACAGAAATAATA[C/T]TGAAAACACAGTGAG | 84708 |
rs12507563 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | LNX1 | GRCh38.p7 | 4:53497027 | AAGGTTTTTTTGCCC[A/G]TGTTCTCAGCAAAAG | 84708 |
rs12507598 | snp | A/G | 0.145305 | 0.227022 | intron-variant | LNX1 | GRCh38.p7 | 4:53473042 | TTGACTATGAAATAC[A/G]GAAGGTGATTTCTTA | 84708 |
rs12507739 | snp | C/T | 0.49621 | 0.0433651 | intron-variant | LNX1 | GRCh38.p7 | 4:53486601 | CAGATGGGAGTGCCA[C/T]GAAAGAGAAATGGGG | 84708 |
rs12508701 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | LNX1 | GRCh38.p7 | 4:53487076 | TTCCAAAATCCACTA[C/T]GGCTGATGAAAACTG | 84708 |
rs12510820 | snp | A/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53639932 | cagctacttgggagg[A/C]tgaggcacaaaaatt | 84708 |
rs12511088 | snp | A/G | 0.498437 | 0.0279115 | intron-variant | LNX1 | GRCh38.p7 | 4:53497095 | AAAGGAAGTTTCCAG[A/G]CTCTTTTATTGAAAG | 84708 |
rs12511253 | snp | A/G | 0.498437 | 0.0279115 | intron-variant | LNX1 | GRCh38.p7 | 4:53497634 | TAAGCTCCAGTTGAA[A/G]GCCACAAGAATCAAA | 84708 |
rs12512586 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53631898 | GAATCCTTGACTCGG[G/T]GTAATTCTATAGTTG | 84708 |
rs12641312 | snp | C/T | 0.298905 | 0.24517 | intron-variant | LNX1 | GRCh38.p7 | 4:53583974 | CAACAACAACAACAA[C/T]GACAAATGAAGGCAG | 84708 |
rs12641948 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53574994 | TTCGTTTTTTTTTTT[C/T]CTTTTTAGACGGAGT | 84708 |
rs12642403 | snp | C/T | 0.499839 | 0.00898417 | intron-variant | LNX1 | GRCh38.p7 | 4:53495473 | GTTTCCAAGTGCTTT[C/T]GAAGTCACCTGGACT | 84708 |
rs12642437 | snp | C/T | 0.464947 | 0.127663 | intron-variant | LNX1 | GRCh38.p7 | 4:53495625 | TCAGCTCACTGCAAC[C/T]TCCGCCTCCCAGTTT | 84708 |
rs12643324 | snp | G/T | 0.449473 | 0.150701 | intron-variant | LNX1 | GRCh38.p7 | 4:53471041 | ttgccaagtcaatcc[G/T]aagccaaaggaacaa | 84708 |
rs12645694 | snp | C/T | 0.28052 | 0.24813 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53499140 | ATTTCTCATGGCACT[C/T]AACCCATTATTGTTA | 84708 |
rs12646532 | snp | G/T | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53618771 | taatactgtatttta[G/T]ctaactaaatatatc | 84708 |
rs12647093 | snp | C/T | 0.313326 | 0.241847 | intron-variant | LNX1 | GRCh38.p7 | 4:53551184 | ACATAAGGCTGCCCA[C/T]AACTCTTACCGCTTT | 84708 |
rs12648881 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53568243 | attgatgcaaaaatc[C/T]tcaataaaatactgg | 84708 |
rs12648929 | snp | A/C | 0.49975 | 0.0111793 | intron-variant | LNX1 | GRCh38.p7 | 4:53568395 | agccaaagacaaaaa[A/C]cacatgattatctca | 84708 |
rs12650358 | snp | A/C | 0.499 | 0.0223418 | intron-variant | LNX1, LOC101928879 | GRCh38.p7 | 4:53575437 | TTTCAAGCGCCAACT[A/C]TGAGCTAGGTCATGA | 84708 |
rs12651687 | snp | C/T | 0.26271 | 0.249677 | intron-variant | LNX1 | GRCh38.p7 | 4:53471289 | aactggctagccata[C/T]gtagagagctgaaac | 84708 |
rs13106967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LNX1 | GRCh38.p7 | 4:53572647 | TGGTATGATTGTTCA[C/T]CCTTTATTAAGCACC | 84708 |
rs13109280 | snp | A/G | 0.408871 | 0.193029 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514346 | atttttacactgcca[A/G]taaagacatacccaa | 84708 |
rs13110880 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53636461 | TTGTCCCTCAGAGTA[A/G]AAAAAGGAGGGCTCT | 84708 |
rs13110894 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53636483 | GAGGGCTCTGAGGCA[A/G]AAGGGCTTGAGTGAC | 84708 |
rs13117240 | snp | A/G | 0.455977 | 0.141681 | intron-variant | LNX1 | GRCh38.p7 | 4:53484195 | gccacctaggatagt[A/G]tattttgttatagca | 84708 |
rs13118038 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | LNX1 | GRCh38.p7 | 4:53491801 | ACGATACTTTTTTTT[G/T]TTTGTTTGTTTTTTG | 84708 |
rs13119372 | snp | C/T | 0.459118 | 0.137002 | intron-variant | LNX1 | GRCh38.p7 | 4:53484511 | GAGGTTGCAGCGAAC[C/T]GAGATTGTGGCACTG | 84708 |
rs13125807 | snp | C/T | 0.278664 | 0.248351 | intron-variant | LNX1 | GRCh38.p7 | 4:53485053 | CGTGAAGAAAGCTGA[C/T]ATGAAGAACGATGGA | 84708 |
rs13127018 | snp | A/G | 0.252421 | 0.249988 | intron-variant | LNX1 | GRCh38.p7 | 4:53571924 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 84708 |
rs13127096 | snp | A/G | 0.498277 | 0.0293024 | intron-variant | LNX1 | GRCh38.p7 | 4:53564694 | CCCAGCCTGAGCGAC[A/G]CAGAAGACGGGTGAT | 84708 |
rs13127527 | snp | A/G | 0.497121 | 0.0378299 | intron-variant | LNX1 | GRCh38.p7 | 4:53564887 | aaagaaaggggtgac[A/G]gacagcaccgggaaa | 84708 |
rs13132250 | snp | C/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53493571 | GTACAGGACAGTGCA[C/G]AGAGTTGCCAGCACC | 84708 |
rs13132690 | snp | C/T | 0.49823 | 0.0296997 | intron-variant | LNX1 | GRCh38.p7 | 4:53564667 | GAATAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 84708 |
rs13139195 | snp | C/G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53565403 | actgacacctcacac[C/G/T]gcagggtactccaac | 84708 |
rs13144237 | snp | C/T | 0.299916 | 0.244966 | intron-variant | LNX1 | GRCh38.p7 | 4:53570802 | ggaggctgaggcggg[C/T]ggatcacgaggtcag | 84708 |
rs13146347 | snp | C/T | 0.484138 | 0.0876334 | intron-variant | LNX1 | GRCh38.p7 | 4:53631438 | ACATTTGATAGGAAA[C/T]GTGACCAAGTTGGCT | 84708 |
rs13146668 | snp | A/G | 0.294576 | 0.245994 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53519757 | TCATTTAATCTTCAC[A/G]ACAACCTCATGAGAT | 84708 |
rs13147284 | snp | A/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53607914 | taactggctagccag[A/T]tgcggaagattgaaa | 84708 |
rs13148245 | snp | A/G | 0.484561 | 0.0864924 | intron-variant | LNX1 | GRCh38.p7 | 4:53625165 | TTGTGACCTTGGATT[A/G]GGCAACGGTTTCTCA | 84708 |
rs13148249 | snp | A/T | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594887 | ctgctagtttttaaa[A/T]tttttctagagatga | 84708 |
rs13150384 | snp | A/T | 0.499325 | 0.0183582 | intron-variant | LNX1 | GRCh38.p7 | 4:53491290 | AAAAAAAAAAAAATC[A/T]TGCTAAGAATGCAGT | 84708 |
rs13150586 | snp | C/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53564128 | TGGTTTCTCTCCTCA[C/G]TGCTGTTTTCCAAAA | 84708 |
rs13150596 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53564139 | CTCACTGCTGTTTTC[C/T]AAAAGTGCATCTCAT | 84708 |
rs13151819 | snp | C/G | 0.4983 | 0.0291038 | intron-variant | LNX1 | GRCh38.p7 | 4:53564685 | TCTACAGCTCCCAGC[C/G]TGAGCGACACAGAAG | 84708 |
rs13353796 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | LNX1 | GRCh38.p7 | 4:53636490 | CTGAGGCAGAAGGGC[C/T]TGAGTGACCTTAAGC | 84708 |
rs13435672 | snp | A/G | 0.215144 | 0.247558 | intron-variant | LNX1 | GRCh38.p7 | 4:53465539 | gggagccagtactcc[A/G]gaaagttttacaatc | 84708 |
rs17082837 | snp | A/T | 0.257454 | 0.249889 | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461359 | TAAATACATGCCTTA[A/T]CTCAAATGGGGCCAA | 84708 |
rs17082847 | snp | C/G | 0.316485 | 0.240998 | intron-variant | LNX1 | GRCh38.p7 | 4:53465396 | TATCTAATGCACTAG[C/G]CTTTATGTAGTCACA | 84708 |
rs17082887 | snp | A/T | 0.084364 | 0.187256 | intron-variant | LNX1 | GRCh38.p7 | 4:53486710 | AAAAAGAGGGTTAAA[A/T]CTAAGTAGCGTCTGT | 84708 |
rs17082893 | snp | A/G | 0.49334 | 0.057322 | intron-variant | LNX1 | GRCh38.p7 | 4:53487108 | TCATACTGTCAGGGC[A/G]TAACATAGATTTGCA | 84708 |
rs17082910 | snp | A/G | 0.250732 | 0.249999 | intron-variant | LNX1 | GRCh38.p7 | 4:53491474 | AAGCTCTACCAGGCC[A/G]GGAACTGTACCAACC | 84708 |
rs17082923 | snp | C/T | 0.498277 | 0.0293024 | intron-variant | LNX1 | GRCh38.p7 | 4:53497314 | TGAGGAAAGAGGCCC[C/T]ATGGAGGAGAAATAA | 84708 |
rs17082936 | snp | C/T | 0.095934 | 0.196885 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501055 | ATGTTAGAGCAACAC[C/T]AATGAGATCCTAGTG | 84708 |
rs17082944 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521529 | CGTGTCATGCAAAGA[C/T]AGCTGGTTCCTCATA | 84708 |
rs17082949 | snp | A/G | 0.16028 | 0.233346 | intron-variant | LNX1 | GRCh38.p7 | 4:53526915 | TTTATAAAATTATAG[A/G]GCTAATTCTTCTTTG | 84708 |
rs17082951 | snp | A/G | 0.394904 | 0.203722 | intron-variant | LNX1 | GRCh38.p7 | 4:53526948 | AGAGACACAATCATT[A/G]TGCTAAAGCAATAGA | 84708 |
rs17082953 | snp | C/T | 0.372189 | 0.218105 | intron-variant | LNX1 | GRCh38.p7 | 4:53527926 | CCAGCAATTAGGTGA[C/T]GTTTATGGTCTAATA | 84708 |
rs17082954 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | LNX1 | GRCh38.p7 | 4:53529383 | GTCCAGAGAACTAGA[G/T]GCCATTGCAACAGAA | 84708 |
rs17082957 | snp | A/T | 0.410399 | 0.191761 | intron-variant | LNX1 | GRCh38.p7 | 4:53529845 | CCACAGGAAATGAAC[A/T]TACACCATCCAAGGG | 84708 |
rs17082962 | snp | A/G | 0.151668 | 0.229849 | intron-variant | LNX1 | GRCh38.p7 | 4:53532110 | TACAACTATGCAATG[A/G]CTTAAGTTCTTAAGA | 84708 |
rs17082966 | snp | A/G | 0.303187 | 0.244277 | intron-variant | LNX1 | GRCh38.p7 | 4:53533134 | TGCCTTCTGGACAGC[A/G]CAGTGGGCCTGGCCT | 84708 |
rs17082975 | snp | A/C/T | 0.0134912 | 0.0810629 | intron-variant | LNX1 | GRCh38.p7 | 4:53536271 | GAAATACCTAACAAT[A/C/T]TCTTCCAGTGCCCAA | 84708 |
rs17082977 | snp | C/T | 0.173965 | 0.238157 | intron-variant | LNX1 | GRCh38.p7 | 4:53537731 | CATTAGGCTGTGCCC[C/T]GAGTTCCACAGGAGC | 84708 |
rs17082994 | snp | C/G | 0.151001 | 0.229563 | intron-variant | LNX1 | GRCh38.p7 | 4:53542262 | ACAAAGGACAGTTTG[C/G]ATTTAAATGATCACA | 84708 |
rs17083013 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | LNX1 | GRCh38.p7 | 4:53549734 | CAATTGCTGAAGATG[C/G]GTATAGGCCACATGG | 84708 |
rs17083031 | snp | A/G/T | 0.0275754 | 0.114207 | intron-variant, utr-variant-5-prime | LNX1 | GRCh38.p7 | 4:53558195 | GCAAGGAGCCACCAC[A/G/T]GTTGGCGAGAGAGCT | 84708 |
rs17083033 | snp | A/T | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53558689 | CATAAAGTTCTGTCC[A/T]AACAATGTACAGGTT | 84708 |
rs17083038 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559051 | CTCAAGACCAGAATC[C/T]TAATAGAAATGGCTC | 84708 |
rs17083041 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LNX1 | GRCh38.p7 | 4:53561628 | TAAAGGTCAACAGAC[A/G]ATCCAGGTTAGACCT | 84708 |
rs17083043 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LNX1 | GRCh38.p7 | 4:53562172 | AATAAGTCTCGCTCA[A/G]GATCAAGAAGTAAAA | 84708 |
rs17083046 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | LNX1 | GRCh38.p7 | 4:53564235 | CTGCATGGGCTAAGG[G/T]TGAATGAAATTCCCA | 84708 |
rs17083051 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | LNX1 | GRCh38.p7 | 4:53572509 | TCCCAAAAGACAAAG[A/G]CTCAGATTCATGACC | 84708 |
rs17083057 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53574076 | AGTCAAGATCTAGGA[A/G]ACATCCACACACCTA | 84708 |
rs17083065 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | LNX1, LOC101928879 | GRCh38.p7 | 4:53575425 | TCAATAAATAGTTTT[C/T]AAGCGCCAACTCTGA | 84708 |
rs17083069 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53577111 | TATCTATGCAGCTGC[C/T]GATTGTCCTCAAGGC | 84708 |
rs17083076 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | LNX1 | GRCh38.p7 | 4:53579872 | GCATGTGGCAACGAT[A/T]ATTTTACGTGTTCTT | 84708 |
rs17083082 | snp | C/T | 0.25634 | 0.24992 | intron-variant | LNX1 | GRCh38.p7 | 4:53581248 | TTATTTTTTAATGGC[C/T]AATTTTTTTCAGATC | 84708 |
rs17083088 | snp | C/T | 0.413748 | 0.188909 | intron-variant | LNX1 | GRCh38.p7 | 4:53582407 | CAAAAGATCACAAAA[C/T]GACCGGATCCTGTAA | 84708 |
rs17083094 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | LNX1 | GRCh38.p7 | 4:53584406 | AAAAAATGTAAAAAC[A/G]CTGCAAGAGAATACA | 84708 |
rs17083100 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | LNX1 | GRCh38.p7 | 4:53584463 | CCAAGACAGGAGCCA[C/T]GGACAAGCTTTGGAG | 84708 |
rs17083112 | snp | C/T | 0.234692 | 0.249531 | intron-variant | LNX1 | GRCh38.p7 | 4:53587509 | TCAGTACATAAATAT[C/T]AGGAATAGTTGTATG | 84708 |
rs17083154 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594423 | AGTGGCCATAAGAAC[A/G]TGGAACTGCATACAT | 84708 |
rs17083167 | snp | C/T | 0.250732 | 0.249999 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53596053 | TACCATCATATTGGC[C/T]GTAATTACTTTTTTA | 84708 |
rs17083170 | snp | C/T | 0.251296 | 0.249997 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53597003 | CTGGTTCCTGGACTC[C/T]GGGAGGCTGCCCAAG | 84708 |
rs17083184 | snp | C/T | 0.113685 | 0.209567 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599021 | TGCAGTTACATGAGA[C/T]AGCAGGCCAGATTGT | 84708 |
rs17083188 | snp | C/G | 0.47743 | 0.103805 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53600303 | ACTCGAGGACACATG[C/G]ACACAAAAAAAAGTC | 84708 |
rs17083195 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | LNX1 | GRCh38.p7 | 4:53616304 | CCTATATACCATACA[C/T]TTAAAAGCTCATAGG | 84708 |
rs17083199 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | LNX1 | GRCh38.p7 | 4:53617057 | TCTGTGCTTGTGCCA[A/G]TTACTATAGAAAGTT | 84708 |
rs17083202 | snp | C/T | 0.029116 | 0.117091 | intron-variant | LNX1 | GRCh38.p7 | 4:53617541 | TCCATCCTTCTGCTT[C/T]ATGACATGGATACTA | 84708 |
rs17083205 | snp | A/G | 0.262159 | 0.249704 | intron-variant | LNX1 | GRCh38.p7 | 4:53617981 | TTCTCTAGTAGTGTG[A/G]TTAGGTGTTTGATTA | 84708 |
rs17083214 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | LNX1 | GRCh38.p7 | 4:53621869 | TTGGACCTTTCATTT[A/C]ACCCCCACCGGATTT | 84708 |
rs17083218 | snp | A/G | 0.495445 | 0.0475058 | intron-variant | LNX1 | GRCh38.p7 | 4:53624719 | CCCTGGGGGTCTTTC[A/G]CCTTGACCTTTCTGC | 84708 |
rs17083248 | snp | C/T | 0.324382 | 0.238678 | intron-variant | LNX1 | GRCh38.p7 | 4:53651557 | ACATTTGTCAGAATA[C/T]GTGGCCAAGAATGTA | 84708 |
rs17520800 | snp | A/C | 0.496348 | 0.0425753 | intron-variant | LNX1 | GRCh38.p7 | 4:53472554 | AAAAGTGGGAAGTGA[A/C]ATCTTACAACATGCC | 84708 |
rs17657105 | snp | A/T | 0.212122 | 0.247114 | utr-variant-3-prime, downstream-variant-500B | LNX1, FIP1L1 | GRCh38.p7 | 4:53460383 | GTATTTGAAAGAATA[A/T]ATTACTAGGATCTTT | 84708 |
rs17658423 | snp | A/T | 0.21695 | 0.247806 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53505870 | AGGAACGTGAATGCC[A/T]GCTGAAAGGAGAGTG | 84708 |
rs17660061 | snp | C/T | 0.498611 | 0.0263212 | intron-variant | LNX1 | GRCh38.p7 | 4:53544504 | CGGCCTGAGAGGTGC[C/T]GATTTCTTTTGTGAT | 84708 |
rs17660253 | snp | G/T | 0.356597 | 0.226135 | intron-variant | LNX1 | GRCh38.p7 | 4:53548198 | GCCAAGTTTTATTTG[G/T]CCTGCAGAAGTAGAC | 84708 |
rs17660502 | snp | A/G | 0.120326 | 0.21374 | intron-variant | LNX1 | GRCh38.p7 | 4:53551933 | ATGATTTAGGTTTCA[A/G]AATTGGAATTGCTCA | 84708 |
rs17661998 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53600650 | GACTTTTCTCAAATC[A/G]CGAGCATGTGAAGAC | 84708 |
rs17663341 | snp | A/C | 0.1652 | 0.235179 | intron-variant | LNX1 | GRCh38.p7 | 4:53647493 | TTCTAACCAAGAGAT[A/C]TTTTTCTGTATATAT | 84708 |
rs17663485 | snp | C/T | 0.163236 | 0.234461 | intron-variant | LNX1 | GRCh38.p7 | 4:53651333 | GCATTCCTTGGGCAC[C/T]GGACTTGCACCACGC | 84708 |
rs17716956 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | LNX1 | GRCh38.p7 | 4:53549912 | CATGGAACTAGAAAG[A/G]CAAGCACAATTTGCC | 84708 |
rs17717318 | snp | A/G | 0.0422008 | 0.138995 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53558388 | AGACCCCACGGTGTG[A/G]ATAATTAAATAATGA | 84708 |
rs17717891 | snp | A/G | 0.107694 | 0.205546 | intron-variant | LNX1 | GRCh38.p7 | 4:53583434 | GCCGCCAAGGTCGTG[A/G]TTAGCTCTGCTTCTG | 84708 |
rs17730883 | snp | C/G | 0.170408 | 0.236992 | intron-variant | LNX1 | GRCh38.p7 | 4:53645680 | GATTGAGATCAGCAG[C/G]AACAAGGGGTCTACA | 84708 |
rs17730986 | snp | C/T | 0.163236 | 0.234461 | intron-variant | LNX1 | GRCh38.p7 | 4:53650260 | TAGGGCTGAGCAAAG[C/T]AGGCACCTGTGCGGG | 84708 |
rs28367315 | snp | C/T | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594742 | TTTAGAGACAACTCT[C/T]CCTTTGTCATCCAAG | 84708 |
rs28386887 | snp | A/G | 0.268452 | 0.249318 | intron-variant | LNX1 | GRCh38.p7 | 4:53561298 | AATGGGGCGATCTTG[A/G]CTCATTGCAACCTCC | 84708 |
rs28392904 | snp | C/G | 0.500493 | 0.0223575 | intron-variant, missense | LNX1, LOC101928879 | GRCh38.p7 | 4:53575675 | TCTGCATCTGGGACC[C/G]ACCCCCTGGGCTGGC | 84708 |
rs28404076 | snp | A/C | 0.447032 | 0.153878 | intron-variant | LNX1 | GRCh38.p7 | 4:53488040 | GTGAAGGCACTGGTT[A/C]CATAAAATTAGAAAG | 84708 |
rs28414913 | snp | A/G | 0.496348 | 0.0425753 | intron-variant | LNX1 | GRCh38.p7 | 4:53472886 | GTTGTAAAGCTGGAA[A/G]AGGCTAAGGTGAAAT | 84708 |
rs28445760 | snp | G/T | 0.178785 | 0.239642 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53602225 | CATCACCATCTATTC[G/T]AGGTCCTGCAAGCAA | 84708 |
rs28452451 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53522189 | TCCCTCTTCACATCA[A/G]ACCCATCTCTACCAC | 84708 |
rs28453205 | snp | G/T | 0.046775 | 0.145601 | intron-variant | LNX1 | GRCh38.p7 | 4:53628413 | TCACTAATCATCAGA[G/T]AAATGCAAATTAAAA | 84708 |
rs28470376 | snp | C/T | 0.371177 | 0.218669 | intron-variant | LNX1 | GRCh38.p7 | 4:53611592 | GCTAGTTACTAGAAC[C/T]GTCTATAAACCCATC | 84708 |
rs28475085 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515749 | TCATGGGAGGGTCTT[C/G]TAAGAAAGATGGCAC | 84708 |
rs28477259 | snp | C/G | 0.295343 | 0.245854 | intron-variant | LNX1 | GRCh38.p7 | 4:53526936 | TTCTTCTTTGTAAGA[C/G]ACACAATCATTATGC | 84708 |
rs28502573 | snp | A/G | 0.317933 | 0.240593 | intron-variant | LNX1 | GRCh38.p7 | 4:53532684 | GAAGTTCCAACCACA[A/G]GAGACAGACTAAACA | 84708 |
rs28503674 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | LNX1 | GRCh38.p7 | 4:53630700 | ACATATATTAGATGC[A/G]GTGTATTTAAATAGG | 84708 |
rs28525154 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | LNX1 | GRCh38.p7 | 4:53535792 | TTCATAGTAATTCAA[C/T]AGATGAATTACTTCT | 84708 |
rs28532143 | snp | A/G | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594157 | TATATATATATATAT[A/G]TATATATAAATATGT | 84708 |
rs28547005 | snp | C/T | 0.310632 | 0.242536 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53523716 | ACAGTTTTTGCATCT[C/T]CAAATGAAGACAGAC | 84708 |
rs28551603 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | LNX1 | GRCh38.p7 | 4:53551260 | TTAGACAGACATGAG[A/G]CAGGGAAGGCCACCC | 84708 |
rs28571951 | snp | A/G | 0.030665 | 0.119967 | intron-variant | LNX1 | GRCh38.p7 | 4:53640144 | AATGACAGTGGTGGT[A/G]GGAGTATAGGTTTTT | 84708 |
rs28591554 | snp | A/G | 0.21695 | 0.247806 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53504787 | TGTATCAGGGAATAC[A/G]GAGGCCCAAGAAGAG | 84708 |
rs28600096 | snp | A/T | 0.029116 | 0.117091 | utr-variant-5-prime, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53652485 | TCTCTTCTGGTTTGG[A/T]TGGGGCTGAGACGCC | 84708 |
rs28608184 | snp | A/G | 0.478685 | 0.10101 | intron-variant | LNX1 | GRCh38.p7 | 4:53611012 | ATGAAACTTGATGGT[A/G]GCAAATTTTAAAACT | 84708 |
rs28634891 | snp | A/G | 0.147991 | 0.228242 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515776 | GCACAGCACGGAGGA[A/G]AAAGCACATGCTTTC | 84708 |
rs28644315 | snp | C/T | 0.21725 | 0.247846 | intron-variant | LNX1 | GRCh38.p7 | 4:53493094 | CCTACCTCAGCCTCC[C/T]AAGTAGCTGGAATTA | 84708 |
rs28683707 | snp | A/G | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594159 | TATATATATATATGT[A/G]TATATAAATATGTAT | 84708 |
rs28688817 | snp | A/C | 0.030278 | 0.119257 | intron-variant | LNX1 | GRCh38.p7 | 4:53649112 | AAGGTTCTGATTTTA[A/C]TCAAGATAACAACTT | 84708 |
rs28708557 | snp | C/T | | | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53576696 | TCAACTTTCCTCTTT[C/T]CCAAAAGTAAATTAA | 84708 |
rs28716804 | snp | G/T | 0.278664 | 0.248351 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511033 | TTGAGTCCAGGAAAG[G/T]AAAACCTCATAAGGT | 84708 |
rs28770180 | snp | C/G | 0.338296 | 0.233889 | intron-variant | LNX1 | GRCh38.p7 | 4:53467734 | TCAACTGGAAGAAAG[C/G]GTATCAGCGATGGAA | 84708 |
rs28778963 | snp | C/G | 0.338296 | 0.233889 | intron-variant | LNX1 | GRCh38.p7 | 4:53472324 | GGGGAACATCACACA[C/G]CGGGGACTGTTGTGG | 84708 |
rs28828807 | snp | C/G | 0.257454 | 0.249889 | intron-variant | LNX1 | GRCh38.p7 | 4:53468522 | GTAAATGGGCTAAAT[C/G]CTCCAATTAAAAGAC | 84708 |
rs28859306 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | LNX1 | GRCh38.p7 | 4:53467008 | TAGTGGTTCTCCCAG[C/G]AAGCAGCTTGAGATC | 84708 |
rs33917709 | in-del | -/GAA | | | intron-variant | LNX1 | GRCh38.p7 | 4:53463639 | AATTTAGGCCTATCG[-/GAA]AAGATTTGGCATAGT | 84708 |
rs33929475 | in-del | -/G | 0.442385 | 0.15965 | intron-variant | LNX1 | GRCh38.p7 | 4:53528681 | ATTCCCTGTGGATAA[-/G]GGGGGGACTACTGTA | 84708 |
rs33931174 | in-del | -/AGTAGGGAGAGT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53582097 | ATTTTAGAAACCTAA[-/AGTAGGGAGAGT]GAATATCAAAACTGT | 84708 |
rs33939700 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | LNX1 | GRCh38.p7 | 4:53652114 | TGGGCAGAGGTGAAG[-/T]TTTTTTTTAAATTGT | 84708 |
rs33945453 | in-del | -/G | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501305 | TTTTTTTTTGGGGGT[-/G]GGGGGGACAGGATCT | 84708 |
rs33962722 | in-del | -/T | 0.472147 | 0.114677 | intron-variant | LNX1 | GRCh38.p7 | 4:53535110 | GAAATAGCACCAATG[-/T]TTTTCTCTCTGCATC | 84708 |
rs33990432 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53541149 | TCAAAAAAAAAAGAA[-/G]AAAAAAAAAAAGAAA | 84708 |
rs33996308 | in-del | -/A | 0.258288 | 0.249863 | intron-variant | LNX1 | GRCh38.p7 | 4:53561928 | GTGTATCCCAGAATT[-/A]AAAAAAAAGGAAAAA | 84708 |
rs34020688 | in-del | -/AA | 0.499994 | 0.00179711 | intron-variant | LNX1 | GRCh38.p7 | 4:53491274 | AGTTTTCAAAGTGAG[-/AA]AAAAAAAAAAAATCT | 84708 |
rs34027088 | in-del | -/A | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53595443 | AAAGAAACTCAGTAT[-/A]CTTGGGCATGGGGTA | 84708 |
rs34028346 | snp | A/G | 0.24932 | 0.249999 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502527 | TTTTGCTGGTAGAGA[A/G]TCTTGCCTTGATGTT | 84708 |
rs34040981 | in-del | -/G | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509440 | TTTTTACTGCCCATA[-/G]GAATCATAGAAATGG | 84708 |
rs34042416 | in-del | -/T | 0.437965 | 0.164831 | intron-variant | LNX1 | GRCh38.p7 | 4:53626794 | GTTTCAGAAAAGAGC[-/T]TTATAATCATAAAAA | 84708 |
rs34062365 | snp | A/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53651437 | CAGGAATGGAAGTAA[A/C]CAGGAATACATGACA | 84708 |
rs34078132 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53623344 | AGTAGCTGGGACCCA[-/C]CCTCAGCTTCCCAAG | 84708 |
rs34081904 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53549795 | ATTGTTTGTAGTTTT[-/C]CCATTATAAGTTAAA | 84708 |
rs34102583 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53615461 | CTGTAGAGAAGCTTA[G/T]CCTAGCTCCCTCGTG | 84708 |
rs34130317 | in-del | -/C | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53520201 | AGCCTCTCACAGCAA[-/C]CCCTGCGGGTCCAAA | 84708 |
rs34139836 | snp | A/G | 0.420255 | 0.183066 | intron-variant | LNX1 | GRCh38.p7 | 4:53569850 | CATCAAAAAGTGGGC[A/G]AAGGACATGAACAGA | 84708 |
rs34145850 | in-del | -/A | 0.498084 | 0.0308911 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53574450 | TCAGATCAGGACAAG[-/A]AAAAAAAAACAAAAA | 84708 |
rs34173531 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53617960 | TCTATATATTAACAA[-/T]TTATTTTCTCTAGTA | 84708 |
rs34184442 | in-del | -/T | 0.489376 | 0.0721049 | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53574983 | CCATTAGATATTTCG[-/T]TTTTTTTTTTTCTTT | 84708 |
rs34190946 | snp | A/G | 0.444444 | 0.157135 | intron-variant | LNX1 | GRCh38.p7 | 4:53633638 | CTGAACTAGTGTTTA[A/G]CCAGGGAAGGCTATG | 84708 |
rs34238618 | snp | A/G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53647577 | TGCTAAGAAAAAAAA[A/G/T]CCAGGATTCATTGGC | 84708 |
rs34252813 | in-del | -/G | | | upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53653577 | CTGATTTACAAACAA[-/G]GGAAGTACACTGCAA | 84708 |
rs34273943 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53473745 | CATCTGTACAACAAA[-/C]CCCCTGTGACATGAG | 84708 |
rs34286011 | multinucleotide-polymorphism | CA/GG | | | intron-variant | LNX1 | GRCh38.p7 | 4:53614820 | CTTCAGCCTCCTGGT[CA/GG]TGGAGCAATTTCCTT | 84708 |
rs34296513 | snp | A/G | 3.32984e-05 | 0.00408021 | missense, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461474 | GGTGTTCCTTCAACA[A/G]TGGATTTGATGAAAA | 84708 |
rs34296777 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53586770 | AAATTGGTGGATCAT[-/A]CTTGTCTACCTTCTA | 84708 |
rs34314995 | snp | C/T | 0.375 | 0.216506 | intron-variant | LNX1 | GRCh38.p7 | 4:53608178 | CCATTTTGTAGGTTG[C/T]CTGTTCACTCTGATG | 84708 |
rs34332829 | snp | C/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53620427 | GGGGATTCTAATGCA[C/G]GCTAACATTTGAGAA | 84708 |
rs34352093 | in-del | -/G | 0.296619 | 0.245615 | intron-variant | LNX1 | GRCh38.p7 | 4:53547918 | TCCAAGAACCTGACA[-/G]GGGACCTACCAGTTG | 84708 |
rs34425559 | in-del | -/CTCT | 0.252983 | 0.249982 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559858 | CAGAGATGAGGGTCC[-/CTCT]ATGTTGCCCAGGCTG | 84708 |
rs34439137 | in-del | -/A | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53503579 | AGTAAACTATGCTGT[-/A]AAAAGATGTGCTGCC | 84708 |
rs34491662 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53536705 | TGCCTCTAAAGAGAC[-/T]TTTGATTACACTAAG | 84708 |
rs34521924 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53573452 | ACATACAACACAACT[-/C]CCACCAAATGCTATT | 84708 |
rs34557111 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53578609 | CTGAAGAAAAAGATT[-/C]CCTTGATTTCACTGA | 84708 |
rs34572777 | in-del | -/C | 0.497933 | 0.032082 | intron-variant | LNX1 | GRCh38.p7 | 4:53490096 | CTGTTGTCAAATGTT[-/C]TTTGATGAAATGAAT | 84708 |
rs34578891 | snp | A/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53535684 | GCCAGGGAAATGAGT[A/T]GAGTTTCTTGGCTCT | 84708 |
rs34613658 | in-del | -/A | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53504762 | AATTGGCTTAATTTC[-/A]ATACTGTTATGTATC | 84708 |
rs34638149 | in-del | -/G | 0.320335 | 0.239902 | intron-variant | LNX1 | GRCh38.p7 | 4:53551139 | GTGGCTCTGACTCCT[-/G]GGGCCTACCACATTT | 84708 |
rs34644181 | in-del | -/CTAT | 0.0441095 | 0.141807 | intron-variant | LNX1 | GRCh38.p7 | 4:53544555 | GATGAGGTTGAGCTG[-/CTAT]CTGAGTAGAACCCAA | 84708 |
rs34653341 | in-del | -/T | 0.357451 | 0.225731 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53598236 | TTTTACTGACTGTGA[-/T]TTTTTTTTTTTTTTG | 84708 |
rs34689191 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53608506 | AAACGCTTATACACT[-/G]GCTGGTGGGAAGGTA | 84708 |
rs34712660 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53625241 | CATCACAATTAAATA[-/T]TTTTTGAGCCTCCAA | 84708 |
rs34718013 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53542465 | AAGCCCAGCCATGGG[-/A]AAGGTGTTTCAAAGA | 84708 |
rs34733918 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53580067 | ACACTATAGCCACAG[-/C]ACTCTGAGTCAAAAG | 84708 |
rs34735732 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53538252 | CAGGTTTTATCTGCA[-/C]CCCTTTCCACTGGAC | 84708 |
rs34762642 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53547527 | TCACCTTCAGCAGAG[-/T]AGCTACTGGATTACA | 84708 |
rs34766553 | in-del | -/T | 0.0770498 | 0.180522 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502935 | CAATTTGGTCATATC[-/T]TTTTTTTTTTTTTTA | 84708 |
rs34784735 | in-del | -/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53518030 | AAATGTCCCTAGTCC[-/T]TTCCAACCACCACTG | 84708 |
rs34799406 | snp | C/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53647568 | GGTCCACTTTGCTAA[C/G]AAAAAAAAGCCAGGA | 84708 |
rs34811927 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | LNX1 | GRCh38.p7 | 4:53491805 | TACTTTTTTTTGTTT[G/T]TTTGTTTTTTGAGAA | 84708 |
rs34823651 | in-del | -/TA/TAT/TATT | 0.241164 | 0.262744 | utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53460865 | TTCAACTTCTTAGCC[-/TA/TAT/TATT]TATTTGTGATTTTTC | 84708 |
rs34828888 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53589055 | GAGAAGGGTGTTTAT[-/A]CTGTGAGACTGGAGG | 84708 |
rs34832930 | snp | C/T | 0.270621 | 0.249148 | intron-variant | LNX1 | GRCh38.p7 | 4:53624427 | CCTCTCTCTTGCCTG[C/T]CACCATGTAAGACAT | 84708 |
rs34836244 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53579226 | GTAAGAAAGAGTAGT[-/G]GGAGTGGATTGATTC | 84708 |
rs34868847 | in-del | -/T/TT/TTT | 0.41141 | 0.19091 | intron-variant | LNX1 | GRCh38.p7 | 4:53623206 | TTTTTTTTTTTTTTT[-/T/TT/TTT]AGGATGGAGTCTCAC | 84708 |
rs34922679 | in-del | -/A | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53606487 | AAACAAAAAACAAAC[-/A]AAAAAAAAACAGAAC | 84708 |
rs34958811 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53540975 | AACCCTGTCTCTTCT[-/A]AAAATACAAAAATTA | 84708 |
rs34961558 | in-del | -/A | | | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461163 | ATTATGTTAACTTCT[-/A]AATTGAGATATTTCT | 84708 |
rs34984795 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53646889 | TTCCAATTTAACATG[-/T]AGTAAATAAACCACT | 84708 |
rs34994831 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53635957 | GATACGGCCAGTGAT[-/G]GGGGAATTAGAAGCA | 84708 |
rs34995249 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53487900 | AATGATTTTTCAACA[-/G]TATGCTTGTGGGGAT | 84708 |
rs34997379 | snp | A/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53531064 | CAGCTACTCAGGAGG[A/C]TGAGGTGGGAGGATG | 84708 |
rs35005085 | in-del | -/G | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53518810 | GGGCAACTGTAACAT[-/G]GGGACGTAGGGAAAA | 84708 |
rs35052273 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53614822 | CAGCCTCCTGGTCAT[-/G]GGAGCAATTTCCTTC | 84708 |
rs35080915 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53626890 | CCAACAGTCTGAAAT[-/G]GGAAATTGAAGCTAG | 84708 |
rs35082655 | snp | A/G | 0.0279244 | 0.114815 | synonymous-codon, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53498823 | CACCATCTGGAATCA[A/G]GTGGTACAACCTTGG | 84708 |
rs35089532 | snp | C/T | 0.250732 | 0.249999 | intron-variant | LNX1 | GRCh38.p7 | 4:53490895 | CGTGTTTTCCATTTC[C/T]TTTTCAACTAGCTTT | 84708 |
rs35089837 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | LNX1 | GRCh38.p7 | 4:53488174 | CATGCTTCAGTACCC[C/T]CAATGACAGGGAGCT | 84708 |
rs35099227 | in-del | -/AT | 0.241053 | 0.24984 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53506427 | TATATTGGGGAAAAC[-/AT]ATGGGATCTAAGACT | 84708 |
rs35102649 | snp | C/G | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53626708 | CATAAATAGGCAAAC[C/G]AAAAAAAAGAAGGAA | 84708 |
rs35134987 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53619641 | TTGGGTTCTCTCCAA[-/T]TTTTGGCTACTATGA | 84708 |
rs35137755 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53631043 | TGCAGTAAGTGCTCC[-/T]TGGGCCAAAAGTACA | 84708 |
rs35139768 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53549219 | GGGCAACAAGGTCAT[-/A]AAAAGACACTCATCT | 84708 |
rs35155425 | snp | G/T | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53598233 | TTATTTTACTGACTG[G/T]GATTTTTTTTTTTTT | 84708 |
rs35157056 | in-del | -/G | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502230 | CCATCCAAGTCACAT[-/G]GGATTACACTGTCCC | 84708 |
rs35194743 | in-del | -/C | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53503693 | TAAATGAGCACTGGA[-/C]CCCCACCTTAAAATC | 84708 |
rs35208091 | in-del | -/G | | | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53574743 | TCACATCTGTAAAAT[-/G]GGGGATAATCACAGG | 84708 |
rs35227618 | in-del | -/T | 0.381697 | 0.212499 | intron-variant | LNX1 | GRCh38.p7 | 4:53541745 | GCTCAGTCTGAGTCA[-/T]TAAAAAAAAGTAGGC | 84708 |
rs35257705 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53525555 | CTCAGCAGAGCTTAG[-/C]AAATATTTCTGTGCC | 84708 |
rs35270697 | multinucleotide-polymorphism | CT/GC | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509166 | TTTAACTATCTCACT[CT/GC]ACTGTGGGGAGGGTA | 84708 |
rs35290546 | in-del | -/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521139 | TCATGGTGGTGAGGG[-/T]TTTCTAGAAGTCAGA | 84708 |
rs35296509 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53550924 | GGAGGCAAGCAACCT[-/C]CCCCACTTGAAAGCC | 84708 |
rs35307198 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53590182 | TTAGCAACAAGAACT[-/G]GGGCAGATTCTTAGT | 84708 |
rs35313782 | snp | A/G | 0.250732 | 0.249999 | intron-variant | LNX1 | GRCh38.p7 | 4:53495189 | GTATTATTTCTTACA[A/G]TTACATATTAATTGA | 84708 |
rs35313858 | snp | A/T | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53597752 | TCTCCAATTTAGCCA[A/T]TGTCATTTCAAAGGT | 84708 |
rs35325403 | in-del | -/G | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53509785 | GCATGTGTGATTGAT[-/G]GGGGTTGTGAAGTTT | 84708 |
rs35335159 | in-del | -/C | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53605474 | GTTCCCAGTAAATTT[-/C]CCAGTATACAATACA | 84708 |
rs35346829 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53533812 | GCCCCCACAACCAAG[-/T]AATTATCTGGTCCAA | 84708 |
rs35369872 | in-del | -/C | | | intron-variant | LNX1 | GRCh38.p7 | 4:53578998 | GATGTATCACGTTTT[-/C]CAGACATATCAGAGC | 84708 |
rs35388102 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559812 | CCGCCATGCCTGGCT[-/A]AAAAAAAAAAAAAAA | 84708 |
rs35394599 | in-del | -/ATAT | 0.427228 | 0.176324 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594141 | GAAAGTGTGTGTATA[-/ATAT]ATATATATATATGTA | 84708 |
rs35412444 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53617548 | TCTGCTTCATGACAT[-/G]GGATACTACACCACA | 84708 |
rs35416324 | in-del | -/TCTG | | | intron-variant | LNX1 | GRCh38.p7 | 4:53614981 | CCGAAATTTGTTCAT[-/TCTG]CTTTGAACACCGAGA | 84708 |
rs35419549 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53586494 | ATGCGTCAAACACAA[-/G]GAAGCAAATAAGAGT | 84708 |
rs35428205 | snp | A/G | 0.446118 | 0.155041 | intron-variant | LNX1 | GRCh38.p7 | 4:53528686 | CTGTGGATAAGGGGG[A/G]GACTACTGTATAGCC | 84708 |
rs35434372 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53479323 | AAACTTTTCTATGTT[-/A]AAAAAAAGTAACCAT | 84708 |
rs35451950 | in-del | -/T | 0.490287 | 0.0690083 | intron-variant | LNX1 | GRCh38.p7 | 4:53634252 | TCTGTCCAGCTTGGC[-/T]TTTTTTTTTTTTTGA | 84708 |
rs35465297 | in-del | -/G | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53598365 | GCCTCCCAAGTACCT[-/G]GGGACTACAGGCATG | 84708 |
rs35473992 | in-del | -/ATT | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53601493 | CAGTCCTTCTAAGTG[-/ATT]ATTAGGCTGCACCTG | 84708 |
rs35512254 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LNX1, LOC101928879 | GRCh38.p7 | 4:53573418 | TTTTATTAGAATTTT[-/A]AAAAATCCCATAAAC | 84708 |
rs35518541 | snp | G/T | 0.39009 | 0.207062 | intron-variant | LNX1 | GRCh38.p7 | 4:53546008 | GACAGGGTTTCACCA[G/T]GTTGGCCAGGCTGGT | 84708 |
rs35551450 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53560843 | ACCAATATAACATAA[-/T]TTTTCCATTACCTGC | 84708 |
rs35564489 | in-del | -/A | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53518821 | ACATGGGACGTAGGG[-/A]AAAAGCATGGAAAAT | 84708 |
rs35602377 | in-del | -/AAGAACTATAAAAACTACGCATTGTTCATTT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53464489 | TAATCAACATGAAAA[lengthTooLong]AGATGTTTATGGGAG | 84708 |
rs35609145 | in-del | -/G | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511863 | CCATGAAGAGCTCCT[-/G]TTCTGATGCTGAACT | 84708 |
rs35612744 | in-del | -/CAGT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53616722 | CCTTATCAATATGCC[-/CAGT]ATTCACTTTAATTAA | 84708 |
rs35652147 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53638218 | GGCTTCTCTGCTGGG[-/T]TTTGCAGTCATGAGA | 84708 |
rs35655756 | snp | C/T | 0.303438 | 0.244222 | intron-variant | LNX1 | GRCh38.p7 | 4:53572124 | TTGCCCAGTGTGGCT[C/T]CCACTCTCAAACCTG | 84708 |
rs35666872 | in-del | -/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53508796 | TTCTCTGGGCTGGTC[-/T]GGGAGGGCCTCCCTG | 84708 |
rs35678519 | in-del | -/CTAG | 0.0898077 | 0.191933 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512234 | GAGAAATTTGGAAGT[-/CTAG]TTTTCAATGTAAAAT | 84708 |
rs35714937 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53465807 | TGAAACATAGTACCC[-/T]TTTTTACCACAGATT | 84708 |
rs35720384 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53474548 | TGGTGATCACCTTTA[-/T]TGAATGAATCTGAAG | 84708 |
rs35743691 | in-del | -/G | 0.0869089 | 0.189476 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514497 | CAAGAGGGCTTGTGT[-/G]GGGGAACTCTCCTTT | 84708 |
rs35760581 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53526216 | GCACGGCACACTGCT[-/A]CCCTGAACACATTCC | 84708 |
rs35767390 | in-del | -/TGTT | 0.284733 | 0.247575 | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53462355 | TACAGGCCAAGTGTT[-/TGTT]AACTATGTTATAATT | 84708 |
rs35809680 | snp | C/T | 0.314057 | 0.241654 | intron-variant | LNX1 | GRCh38.p7 | 4:53612769 | GCTAGTCTGTACTCC[C/T]AGCTACTCAGGAGGC | 84708 |
rs35840622 | in-del | -/A | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599459 | TTAGCATATATCAAG[-/A]AAATAACCATAAAAA | 84708 |
rs35852395 | in-del | -/AATC/ATCA | | | utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53460625 | GGGGTATACAAATCA[-/AATC/ATCA]TTTTAGTTGTTTTAG | 84708 |
rs35873206 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53529875 | GCAAACACAGTTCTC[-/A]AAAAGCTTCTCTATT | 84708 |
rs35884858 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53514507 | TTGTGTGGGGAACTC[C/T]CCTTTATAAAACCAT | 84708 |
rs35922375 | in-del | -/A | 0.284701 | 0.24758 | intron-variant | LNX1 | GRCh38.p7 | 4:53583553 | CACCCAAAAATACAG[-/A]AAAAAAAAACCCTTT | 84708 |
rs35956527 | snp | A/C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53589164 | TGACAACTGGACATT[A/C/T]CCCCCGAAAGGCCCA | 84708 |
rs35962636 | in-del | -/TCT | 0.350345 | 0.239979 | intron-variant | LNX1 | GRCh38.p7 | 4:53536330 | GATTCTCACTCCACA[-/TCT]TCTTCAAGAGGGGAC | 84708 |
rs35978987 | snp | A/G | 0.49941 | 0.0171624 | intron-variant | LNX1 | GRCh38.p7 | 4:53492652 | CAGCAAAGAGGCTCC[A/G]GCCGTCACTCAGACC | 84708 |
rs35990885 | in-del | -/G | 0.250732 | 0.249999 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53595975 | TCATCTCTACAAAAA[-/G]CCTCTTTGGCTATCT | 84708 |
rs36008958 | in-del | -/G | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594873 | GTGCCACCATGCCCT[-/G]GCTAGTTTTTAAATT | 84708 |
rs36011216 | snp | A/T | 0.495291 | 0.0482933 | intron-variant | LNX1 | GRCh38.p7 | 4:53484559 | GAAAGCAAGACTCCA[A/T]CTCAAAAAAAGAAAA | 84708 |
rs36023492 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53578265 | GTGTTGCTTAATGAT[-/G]GGGGATATGTTCTGA | 84708 |
rs36031525 | snp | A/G | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53602320 | GGGGATGGAGGCTGA[A/G]AAAGGCTGGGAGAGC | 84708 |
rs36087782 | in-del | -/A | | | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53596462 | TTCTTTAGTAGGGAG[-/A]AAAAAAGAACTTCAT | 84708 |
rs36090882 | snp | A/C | 0.249886 | 0.25 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53513225 | AGCCCAGAAGGCAGT[A/C]TGGCAGAAGACAGCT | 84708 |
rs36113346 | snp | G/T | 0.444444 | 0.157135 | intron-variant | LNX1 | GRCh38.p7 | 4:53633631 | GCTTTTCCTGAACTA[G/T]TGTTTAGCCAGGGAA | 84708 |
rs36120084 | in-del | -/T | 0.44768 | 0.153045 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53519439 | CAGTTTTGTTCAGTG[-/T]TTTTTTTTTTTTTTT | 84708 |
rs36120398 | in-del | -/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53580263 | TAGAATATGCCTAAC[-/T]TTTTTAAGTCCTTTA | 84708 |
rs36122073 | in-del | -/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53474392 | ATTCATTCATGTATT[-/G]GCCTGTGGCTGCTCT | 84708 |
rs36125516 | in-del | -/G | | | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53577092 | TTGTTTCAAGGAAAT[-/G]CTGTATCTATGCAGC | 84708 |
rs36213275 | in-del | -/ACCTAGT | 0.477768 | 0.103061 | intron-variant | LNX1 | GRCh38.p7 | 4:53617185 | TGACCAAAAAATAAG[-/ACCTAGT]ACCTAGTCTAATAAT | 84708 |
rs41359948 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53499666 | AGAGGGCAAAGTGGC[A/G]AATTGGTTCTGTTTT | 84708 |
rs55641224 | in-del | -/GGCCCT | 0.478768 | 0.100824 | intron-variant | LNX1 | GRCh38.p7 | 4:53613985 | CTGTTATTTTTTGAC[-/GGCCCT]TTTTTGATAATAGCC | 84708 |
rs55707202 | snp | C/T | 0.163236 | 0.234461 | intron-variant | LNX1 | GRCh38.p7 | 4:53650463 | AAGGATAATGGGAGC[C/T]GGCTTCTGATGAATG | 84708 |
rs55731250 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594689 | CTTTTCTTTTACTTT[C/G]TTACTTTCTTTTCTT | 84708 |
rs55732414 | snp | C/T | 0.110519 | 0.207473 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53599206 | TGGCATTCTAAGTCA[C/T]AGGATGAGATAAAAG | 84708 |
rs55799407 | in-del | -/A | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515513 | CAATTTAAGGCCCCC[-/A]CCCCACCAAAAAAAA | 84708 |
rs55820499 | in-del | -/A | | | intron-variant | LNX1 | GRCh38.p7 | 4:53528151 | ATTTTCCCTTTGAAA[-/A]CTGCTCTTTTGCCAG | 84708 |
rs55823057 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53516704 | CAGACCTGAAGTGAG[A/G]TCCAAGAGGAGCAAC | 84708 |
rs55849518 | snp | C/T | 0.147656 | 0.228091 | nc-transcript-variant, intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53604186 | TTTTGTTCTACCCTT[C/T]GTAGAAGACAATTTG | 84708 |
rs55922219 | snp | A/G | 0.163892 | 0.234703 | intron-variant | LNX1 | GRCh38.p7 | 4:53642725 | AATCAGCAAGCCTGC[A/G]GGGTCTGAGGTTTCC | 84708 |
rs55945634 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LNX1 | GRCh38.p7 | 4:53582312 | AGACACACAGGTGAA[C/T]AGTTTGCTGAAGGGT | 84708 |
rs55949796 | snp | A/G | 0.163236 | 0.234461 | upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53653431 | TCTCTTTCCAGAGAT[A/G]TGAGTCGGGTGCTGG | 84708 |
rs55966837 | snp | C/G | 0.175254 | 0.238565 | intron-variant | LNX1 | GRCh38.p7 | 4:53627226 | ATTGTATGATGGGAA[C/G]AGAGTTTAGAGTTTT | 84708 |
rs55973551 | snp | A/G | 0.487933 | 0.0767327 | intron-variant | LNX1 | GRCh38.p7 | 4:53541147 | AACTCAAAAAAAAAA[A/G]AAAAAAAAAAAAGAA | 84708 |
rs56014502 | snp | G/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501305 | TTTTTTTTTTGGGGG[G/T]GGGGGGACAGGATCT | 84708 |
rs56089202 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | LNX1 | GRCh38.p7 | 4:53590917 | AACAGGTTTTCAGGG[G/T]GAAAGAAAAAAAAAC | 84708 |
rs56148907 | snp | C/T | 0.000399281 | 0.0141238 | missense | LNX1 | GRCh38.p7 | 4:53496024 | GACCTCTGACTCACC[C/T]GAATCAGATGAGCCG | 84708 |
rs56165716 | in-del | -/T/TGG/TGGG | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501299 | TTTTTTTTTTTTTTT[-/T/TGG/TGGG]GGGGGTGGGGGGACA | 84708 |
rs56183605 | snp | A/G | 0.106987 | 0.205054 | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53577071 | GAGGGTGCAGGAGGG[A/G]GTAAAGTTGTTTCAA | 84708 |
rs56201249 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LNX1 | GRCh38.p7 | 4:53561331 | CTCCCAGGTTCAAAC[A/G]ATTCTCCTGCCTCAG | 84708 |
rs56303907 | in-del | -/ACAGAAGTAG | 0.279195 | 0.248289 | intron-variant | LNX1 | GRCh38.p7 | 4:53590515 | ATTGGGCTGTCAAGA[-/ACAGAAGTAG]ATACAGGCTGTGTGA | 84708 |
rs56314005 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | LNX1 | GRCh38.p7 | 4:53640920 | TGTTTTTCTCAGTCT[C/T]GTCGGCAGTCCTTCC | 84708 |
rs56331163 | snp | A/G | 0.294832 | 0.245947 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53508774 | AGCTTGGTGGCTTCC[A/G]TTCTCTTTCTCTGGG | 84708 |
rs56357115 | snp | A/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53502424 | ACAATAGCATGTTTT[A/T]TAAAATGTACATATC | 84708 |
rs56380651 | snp | A/G | 0.151001 | 0.229563 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53517567 | GACCTCCTGTAAAGA[A/G]CTTTCCGAGTTCAGT | 84708 |
rs56388080 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LNX1 | GRCh38.p7 | 4:53538147 | CAATCACAAACTCAC[C/T]CCCAAGCACAGAATC | 84708 |
rs56402228 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | LNX1 | GRCh38.p7 | 4:53614091 | AGCTTCTTTTCATAC[A/G]ATTGTTGGCTGCATG | 84708 |
rs56708336 | snp | C/T | 0.170882 | 0.237579 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53510900 | TAAAAGAAACTGGCA[C/T]CTTTCTCTGCTGCCC | 84708 |
rs56762579 | in-del | -/CAAAAA | 0.0898077 | 0.191933 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512233 | GGAGAAATTTGGAAG[-/CAAAAA]TTTTTCAATGTAAAA | 84708 |
rs56807203 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | LNX1 | GRCh38.p7 | 4:53532873 | TGCAGGCTGCCCAGG[A/G]AGTTGCTGCCAGCAT | 84708 |
rs56852804 | in-del | -/AGA | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53463643 | TAGGCCTATCGAAGA[-/AGA]TTTGGCATAGTATAA | 84708 |
rs56921221 | snp | A/G | 0.168785 | 0.236441 | intron-variant | LNX1 | GRCh38.p7 | 4:53485997 | CAATTTGGGCAAAAG[A/G]ATGGTTTAACAATGG | 84708 |
rs57155745 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LNX1 | GRCh38.p7 | 4:53547015 | CTCTTCAGTGAGAGG[A/G]AGGAAGAGACTGTAT | 84708 |
rs57164667 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53627238 | GAACAGAGTTTAGAG[G/T]TTTTGATGACCTTGG | 84708 |
rs57222437 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53549407 | ATTCCTCAGAATTTA[C/T]TTCAAGAGCTCCTTT | 84708 |
rs57272023 | in-del | -/AACAAC | 0.444799 | 0.156695 | intron-variant | LNX1 | GRCh38.p7 | 4:53583933 | AACTGACCCCCTGCA[-/AACAAC]AACAACAACAACAAC | 84708 |
rs57276714 | snp | A/T | 0.0399052 | 0.1355 | intron-variant, nc-transcript-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53523138 | GATCTCCAACTAGAT[A/T]GAAGAACAGGACCCT | 84708 |
rs57287210 | snp | C/G | 0.166506 | 0.235645 | intron-variant | LNX1 | GRCh38.p7 | 4:53468934 | TAGACAGATCAACGA[C/G]ACAGAAAGTTAACAA | 84708 |
rs57297394 | snp | A/G | 0.499464 | 0.016365 | intron-variant | LNX1 | GRCh38.p7 | 4:53492963 | GCATACACCTCAGAA[A/G]GAAAATGTCTCTTTG | 84708 |
rs57334807 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | LNX1 | GRCh38.p7 | 4:53570888 | AAAAATTAGCTGTGC[A/G]TGGTGGTGGGCACCT | 84708 |
rs57366823 | in-del | -/ATT/TAT | 0.5 | 0 | utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53460866 | ACTTCTTAGCCTATT[-/ATT/TAT]TGTGATTTTTCTGTT | 84708 |
rs57521062 | in-del | -/C | 0.0256215 | 0.110247 | intron-variant | LNX1 | GRCh38.p7 | 4:53584163 | TTTCTGTTGTTGTTG[-/C]TTTTTTTTAAAACAG | 84708 |
rs57587034 | snp | A/T | 0.316726 | 0.240931 | intron-variant | LNX1 | GRCh38.p7 | 4:53475802 | TAATTAAGTGAGACA[A/T]GTAATTACGTCACTG | 84708 |
rs57685463 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53522546 | GTTGCATGGATGTTG[A/G]TTGAGCCTGTTTTAC | 84708 |
rs57853960 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53652957 | GTGGCTGATACTATT[C/T]AAGACTCTTAACTCT | 84708 |
rs57866682 | snp | A/G | 0.340333 | 0.233109 | intron-variant | LNX1 | GRCh38.p7 | 4:53471070 | AAAGCTGGAGGCATC[A/G]CACTACCTGACTTCA | 84708 |
rs57902014 | snp | A/G | | | intron-variant, utr-variant-3-prime | LNX1, LOC101928879 | GRCh38.p7 | 4:53577165 | CAGGAAATACTTTAA[A/G]TGACATCAGAAACAG | 84708 |
rs57911627 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | LNX1 | GRCh38.p7 | 4:53618974 | GCAGGGTGGTCTCTA[A/T]CTCCTGGGCTCAAGT | 84708 |
rs57991612 | snp | A/G/T | 0.0279526 | 0.114869 | intron-variant | LNX1 | GRCh38.p7 | 4:53562572 | GTTTACAAATGAAAC[A/G/T]CATTCTGGAGAAAAC | 84708 |
rs58057416 | in-del | -/ACTA | | | intron-variant | LNX1 | GRCh38.p7 | 4:53616008 | TACTAATTCTTTCTA[-/ACTA]TTTTTTGTATTCATT | 84708 |
rs58208481 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | LNX1 | GRCh38.p7 | 4:53535920 | TCACACCCATTTTAC[C/T]GATGGGGAAGCTCAA | 84708 |
rs58276332 | snp | G/T | 0.341909 | 0.232492 | intron-variant | LNX1 | GRCh38.p7 | 4:53539390 | TTAATTTTTGAGACC[G/T]GTCTCACTCTGTCGC | 84708 |
rs58298942 | snp | A/G | 0.307176 | 0.243374 | intron-variant | LNX1 | GRCh38.p7 | 4:53561807 | TACTAGTAAATACTT[A/G]AGGAGGGTCAGTTTT | 84708 |
rs58497446 | in-del | -/CCGT | | | intron-variant | LNX1 | GRCh38.p7 | 4:53625843 | CCCAGCAATTCCACC[-/CCGT]GTGTGTGTGTGTGTG | 84708 |
rs58611539 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53627135 | ATTTCAAGCTTTGTA[A/G]CCAGCCTTGGTCTCA | 84708 |
rs58628142 | snp | G/T | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501299 | TTTTTTTTTTTTTTT[G/T]GGGGGTGGGGGGACA | 84708 |
rs58686690 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594565 | CCCATACCATTCTCA[C/T]TGTCATTGCTAAAGA | 84708 |
rs58697948 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | LNX1 | GRCh38.p7 | 4:53551371 | TGAAGCCAGGGCCAG[G/T]CAGTTTCCCAATAAA | 84708 |
rs58715153 | in-del | -/AG/AGAGAGAG/AGAGAGAGAG/AGAGAGAGAGAGAG | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53492543 | GAGAGAGAGAGAGAG[lengthTooLong]TGGCATCCTGACTGG | 84708 |
rs58810347 | in-del | -/ATGTGT | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512513 | TGTGTGTGTGTGTGT[-/ATGTGT]GTGTGCATGCAGAGG | 84708 |
rs58886448 | snp | C/T | 0.108048 | 0.20579 | intron-variant | LNX1 | GRCh38.p7 | 4:53628840 | ATGACTTGGACGAAG[C/T]AGGAGGCCATTTTTC | 84708 |
rs58887272 | snp | A/G | 0.166832 | 0.235761 | intron-variant | LNX1 | GRCh38.p7 | 4:53533457 | AGGCTGGAGTGCAGC[A/G]GTGCGTTCTCAGCTC | 84708 |
rs59011653 | in-del | -/A | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53609277 | ACCTAAACTAAAAGT[-/A]AAAAAAAAAGGAAAT | 84708 |
rs59215529 | snp | A/G | 0.487933 | 0.0767327 | intron-variant | LNX1 | GRCh38.p7 | 4:53541148 | ACTCAAAAAAAAAAG[A/G]AAAAAAAAAAAGAAA | 84708 |
rs59227137 | in-del | -/ACTATAAAAACTACGCAT/ACTATAAAAACTACGCATTGTTCATTTAAGA | | | intron-variant | LNX1 | GRCh38.p7 | 4:53464492 | TCAACATGAAAAAGA[lengthTooLong]TGTTTATGGGAGATT | 84708 |
rs59232300 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53520578 | CTGTTATCTGTCCAT[A/G]CATTCAAGTGTGTAT | 84708 |
rs59254887 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | LNX1 | GRCh38.p7 | 4:53606654 | CAGACATACAATAAA[A/C]AAAGAAAACTTCAGG | 84708 |
rs59260730 | in-del | -/A/AAAAAAA/AAAAAAAAA/AAAAAAAAAAAAAAA | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53506875 | AAAAAAAAAAAAAAA[lengthTooLong]GAGGAATAATAGTAG | 84708 |
rs59307089 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | LNX1 | GRCh38.p7 | 4:53636716 | CCTCCACATTTTCCT[A/G]TCAGGGAGCAAACCC | 84708 |
rs59311047 | snp | A/G | 0.338296 | 0.233889 | intron-variant | LNX1 | GRCh38.p7 | 4:53471409 | GAAAACCTAGGCATT[A/G]CCATTCAGGACATAG | 84708 |
rs59366709 | in-del | -/GT/GTGTGT | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53625882 | TGTGTGTGTGTGTGT[-/GT/GTGTGT]ATCCAAGAAAACTGA | 84708 |
rs59440111 | snp | A/T | | | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461344 | CCCCACAAAGTATAA[A/T]AAATACATGCCTTAT | 84708 |
rs59538345 | snp | C/G | 0.271972 | 0.249033 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515510 | CTTCAATTTAAGGCC[C/G]CCACCCCACCAAAAA | 84708 |
rs59585683 | snp | A/G | 0.465052 | 0.127485 | intron-variant | LNX1 | GRCh38.p7 | 4:53495677 | CCTCTTGAGTAGCTA[A/G]GATTACAGGCACCTG | 84708 |
rs59651495 | snp | C/T | 0.181659 | 0.240478 | intron-variant | LNX1 | GRCh38.p7 | 4:53471144 | GTACCAAAACAGAGA[C/T]ATAGACCAATGGAAC | 84708 |
rs59746479 | in-del | -/A/AA | | | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559829 | AAAAAAAAAAAAAAA[-/A/AA]TTAAAATCTTTTTCA | 84708 |
rs59761197 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | LNX1 | GRCh38.p7 | 4:53535878 | TACATTTGATATGAC[C/T]CCTGATAACTGTTGA | 84708 |
rs59780089 | snp | A/C/G | 0.345704 | 0.230956 | intron-variant | LNX1 | GRCh38.p7 | 4:53539389 | TTTAATTTTTGAGAC[A/C/G]TGTCTCACTCTGTCG | 84708 |
rs59822487 | snp | C/T | 0.211516 | 0.24702 | intron-variant | LNX1 | GRCh38.p7 | 4:53525270 | GCGGATCATTTGAGG[C/T]CAGGAGTTTGAGACC | 84708 |
rs59900244 | in-del | -/TTCCTCT | 0.267091 | 0.249415 | intron-variant | LNX1 | GRCh38.p7 | 4:53557781 | TATGTGTGGAATTTA[-/TTCCTCT]AAAATGGATATATCA | 84708 |
rs59935554 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53654140 | ACAAAGAGAAAAAAG[C/T]CTAGGCTTTTACTTA | 84708 |
rs59961961 | snp | C/G | 0.021333 | 0.101051 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521935 | CTCCTGAGTAGCTAG[C/G]ACTACAGGTGTATAC | 84708 |
rs59986222 | snp | G/T | | | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461288 | TATGTGTAATTATTT[G/T]GGATTTCTCAGAAGT | 84708 |
rs60178188 | in-del | -/AAC | | | intron-variant | LNX1 | GRCh38.p7 | 4:53583972 | AACAACAACAACAAC[-/AAC]GACAAATGAAGGCAG | 84708 |
rs60255253 | snp | A/C | 0.258843 | 0.249844 | intron-variant | LNX1 | GRCh38.p7 | 4:53609210 | CATCTGTATACAAAA[A/C]CCCTGTGACATGCAA | 84708 |
rs60271606 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53506213 | TGGGCTAGTTACCTA[A/T]TCCCTCTGGGTCTCC | 84708 |
rs60273663 | in-del | -/ATGTGTGT | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512515 | TGTGTGTGTGTGTGT[-/ATGTGTGT]GTGCATGCAGAGGGG | 84708 |
rs60288851 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | LNX1, LNX1-AS2 | GRCh38.p7 | 4:53592739 | AGGTTTTGGGGTTTG[G/T]TTTGGGGGAGGGTGG | 84708 |
rs60458406 | in-del | -/T | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53519456 | TTTTTTTTTTTTTTT[-/T]AATCACAAGGCATGG | 84708 |
rs60475646 | snp | A/C | 0.488846 | 0.0738428 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53515513 | CAATTTAAGGCCCCC[A/C]CCCCACCAAAAAAAA | 84708 |
rs60495392 | in-del | -/AT/TA | | | intron-variant | LNX1 | GRCh38.p7 | 4:53652036 | AGAGAGAGAGAGAGA[-/AT/TA]GAGAGAGAGAGAGAG | 84708 |
rs60502260 | snp | C/G | 0.039522 | 0.134904 | intron-variant | LNX1 | GRCh38.p7 | 4:53619759 | GGTTACATGGTAATT[C/G]TATGTTTAATTTTTC | 84708 |
rs60566426 | in-del | -/A | 0.441705 | 0.160466 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53517780 | AGAAACTGCACATGG[-/A]AAAAAAGTTATGAGC | 84708 |
rs60601837 | snp | C/T | 0.297382 | 0.245469 | intron-variant | LNX1 | GRCh38.p7 | 4:53585311 | TGAAGGTAGTGATGA[C/T]GGCTGCCAATTCTGA | 84708 |
rs60609514 | snp | C/T | 0.255503 | 0.249939 | intron-variant | LNX1 | GRCh38.p7 | 4:53528490 | TTTTGAGATAGACCA[C/T]GTATGCACAATTATT | 84708 |
rs60680696 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | LNX1 | GRCh38.p7 | 4:53608751 | TAAAAAAAATGTGGT[A/G]CATATTCACCACAGA | 84708 |
rs60708527 | snp | A/G | 0.283421 | 0.247756 | intron-variant | LNX1 | GRCh38.p7 | 4:53497014 | GGTGGTCCCCTGCAA[A/G]GTTTTTTTGCCCATG | 84708 |
rs60776785 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LNX1 | GRCh38.p7 | 4:53649657 | CCACTCCCTTTACTC[A/C]CCTTCTAGTCAGTCT | 84708 |
rs60802297 | in-del | -/TCTG/TCTGACACAC | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53519666 | AGGTATCTGACACAC[-/TCTG/TCTGACACAC]ACACACATGCGCGCA | 84708 |
rs60814046 | snp | A/T | 0 | 0 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501286 | TGATAATAATCTTTT[A/T]TTTTTTTTTTTTTGG | 84708 |
rs60831969 | snp | C/T | 0.215446 | 0.2476 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53499332 | CCTGGCAAATTTTTA[C/T]ATTTTTTGTGGAGAC | 84708 |
rs60909872 | in-del | -/A | 0.288448 | 0.25203 | intron-variant, utr-variant-3-prime | LNX1, FIP1L1 | GRCh38.p7 | 4:53461045 | ATCTAAAAAAAAAAA[-/A]CAAAACAAGATATGA | 84708 |
rs60957722 | snp | A/T | | | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559830 | AAAAAAAAAAAAAAA[A/T]TAAAATCTTTTTCAG | 84708 |
rs60960129 | in-del | -/GC/GGC/GGGC | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501304 | TTTTTTTTTTGGGGG[-/GC/GGC/GGGC]TGGGGGGACAGGATC | 84708 |
rs61052522 | snp | G/T | 0.217551 | 0.247885 | intron-variant | LNX1 | GRCh38.p7 | 4:53489370 | ATCTTTAGATGCAAA[G/T]ACATTAATGATAATA | 84708 |
rs61240802 | snp | A/C | 0.316726 | 0.240931 | intron-variant | LNX1 | GRCh38.p7 | 4:53475801 | GTAATTAAGTGAGAC[A/C]AGTAATTACGTCACT | 84708 |
rs61359128 | snp | A/T | 0.040671 | 0.13668 | intron-variant | LNX1 | GRCh38.p7 | 4:53529745 | GAACTTATTACACAG[A/T]GCAGGTAAGGCTGGG | 84708 |
rs61435460 | snp | C/T | 0.16911 | 0.236552 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53506837 | GCACTCCAGCCTGGG[C/T]GACAAGCAAAACTCT | 84708 |
rs61476881 | in-del | -/G | 0 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53541148 | CTCAAAAAAAAAAGA[-/G]AAAAAAAAAAAGAAA | 84708 |
rs61486411 | in-del | -/CT | 0.338296 | 0.233889 | intron-variant | LNX1 | GRCh38.p7 | 4:53475071 | CACACCCAGCCCAGA[-/CT]CTACTTCCAGCAAAA | 84708 |
rs61739992 | snp | C/T | 0.0920916 | 0.193817 | intron-variant, missense | LNX1, LOC101928879 | GRCh38.p7 | 4:53576014 | CCCTCCATCTTCCCC[C/T]CACCAGCCTGAAGCC | 84708 |
rs62323564 | snp | C/T | 0.166832 | 0.235761 | intron-variant | LNX1 | GRCh38.p7 | 4:53474832 | AGTGCAGTGGCGCGA[C/T]CTCAGCTCACTGCAA | 84708 |
rs62323567 | snp | C/T | 0.167158 | 0.235875 | intron-variant | LNX1 | GRCh38.p7 | 4:53483150 | TTCCCATGCTGTTCT[C/T]GAGATAGTAAGTCTC | 84708 |
rs62323568 | snp | C/T | 0.167809 | 0.236103 | intron-variant | LNX1 | GRCh38.p7 | 4:53483427 | TTCACATGTGTCAGG[C/T]AGTATGGGCCATTAT | 84708 |
rs62323569 | snp | A/G | 0.166832 | 0.235761 | intron-variant | LNX1 | GRCh38.p7 | 4:53484112 | CCCAGACACCAAACC[A/G]GCTAGTGTCTTGATC | 84708 |
rs62323570 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | LNX1 | GRCh38.p7 | 4:53485778 | CTTTCCACTAGTATC[A/T]ATGTGGTGTGAGTGT | 84708 |
rs62323573 | snp | A/T | 0.185155 | 0.241444 | intron-variant | LNX1 | GRCh38.p7 | 4:53489037 | AGTTGATATTCCCTA[A/T]AAAATGAGTTTGGTC | 84708 |
rs62323589 | snp | A/G | 0.185472 | 0.241529 | intron-variant | LNX1 | GRCh38.p7 | 4:53492334 | GCAGAAATGCTTGAA[A/G]AGCACCAAGAAGGCA | 84708 |
rs62323593 | snp | A/G | 0.185472 | 0.241529 | intron-variant | LNX1 | GRCh38.p7 | 4:53497582 | GTCAGGGGAGTCAGG[A/G]TTGCCTGCTAAATAG | 84708 |
rs62323595 | snp | A/G | 0.186105 | 0.241697 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53499631 | AATTGCAGTTTTATC[A/G]CTTGCTTATTGAGAG | 84708 |
rs62323596 | snp | C/T | 0.186105 | 0.241697 | intron-variant, upstream-variant-2KB | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53499723 | AAAGACTCTGCTTTT[C/T]AGGCTTGGGGGAACA | 84708 |
rs62323597 | snp | C/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53500751 | GGTACTAACAGTACT[C/T]GGGTGATTGAGTTCA | 84708 |
rs62323598 | snp | C/T | 0.186421 | 0.24178 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501102 | GGAATTTTTAAACTG[C/T]CAAACTTGTGTTGGT | 84708 |
rs62323599 | snp | A/G | 0.186105 | 0.241697 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53501168 | TACTCAAGGACTAAA[A/G]GATATAATCTTATTA | 84708 |
rs62323601 | snp | A/C | 0.188 | 0.24219 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53511824 | TCTGCAAAGGTCACC[A/C]AACAGGGCAGCGTGA | 84708 |
rs62323602 | snp | C/G | 0.188 | 0.24219 | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512053 | GGGTTCATTAATTGT[C/G]CAGTCTGATCTGACT | 84708 |
rs62323618 | snp | G/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53512486 | CTCCCTACCCAGTGT[G/T]TGTGTGTGTGTGTGT | 84708 |
rs62323620 | snp | C/T | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53519434 | TTGTTCAGTTTTGTT[C/T]AGTGTTTTTTTTTTT | 84708 |
rs62323621 | snp | A/C | | | intron-variant | LNX1, LNX1-AS1 | GRCh38.p7 | 4:53521878 | CATCATAGCTTACCA[A/C]AGCCTCAAACTCCTG | 84708 |
rs62323622 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | LNX1 | GRCh38.p7 | 4:53527437 | TTGCATGAATTCCCC[C/G]ACACCCATAATTAGT | 84708 |
rs62323625 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LNX1 | GRCh38.p7 | 4:53538960 | TGCACAGACAGTCTT[C/T]CATGGCCAAGTCCAG | 84708 |
rs62323644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LNX1 | GRCh38.p7 | 4:53544106 | GCCTAGCTGTCATTG[A/G]GCTTTTAAATTCTCT | 84708 |
rs62323645 | snp | A/G | | | intron-variant | LNX1 | GRCh38.p7 | 4:53544978 | ACCTCAGACCTATGT[A/G]GAGTTTGCATTGCAC | 84708 |
rs62323647 | snp | C/T | 0.252983 | 0.249982 | intron-variant, upstream-variant-2KB | LNX1 | GRCh38.p7 | 4:53559956 | GCAAGCCACTGCACC[C/T]GGGTCTACTGTTACT | 84708 |
rs62323648 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LNX1 | GRCh38.p7 | 4:53562041 | GTCATTTCCTTAGAG[A/G]CAGAAATCACAACTT | 84708 |
rs62323653 | snp | C/T | 0.305685 | 0.24372 | intron-variant | LNX1 | GRCh38.p7 | 4:53569245 | GCTGGAGGCATCACA[C/T]TACCTGACTTCAAAC | 84708 |
rs62323655 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53570232 | ATGTTTATTGCGGCA[C/T]TATTCACAATAGCAA | 84708 |
rs62323656 | snp | C/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53570329 | CCATGGAATACTATG[C/T]AGCCATAAAAAATGA | 84708 |
rs62323658 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | LNX1 | GRCh38.p7 | 4:53572417 | ACTGACATAATGAGC[A/G]TGGAAAACATGTGCT | 84708 |
rs62323659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LNX1 | GRCh38.p7 | 4:53581080 | CAGCTCCAGGTGCTC[C/T]GTGTCCCCACCCCAC | 84708 |
rs62325480 | snp | G/T | 0 | 0 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53594731 | TAATTTTTTTTTTTA[G/T]AGACAACTCTCCCTT | 84708 |
rs62325481 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53597498 | TAAGCACATTCTGGC[C/T]ATGTTCCACCCTTCA | 84708 |
rs62325482 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53598254 | TTTTTTTTTTTTGAG[A/G]CAGGGTCTTGCTTTG | 84708 |
rs62325483 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | LNX1-AS2, LNX1 | GRCh38.p7 | 4:53598694 | GTAAGTCAAGGGAAG[A/G]AATGGAGGAAGGGAG | 84708 |
rs62325484 | snp | A/T | 0.5 | 0 | intron-variant | LNX1 | GRCh38.p7 | 4:53609549 | TCATAAATTTATAAT[A/T]TATGTATAAATAATA | 84708 |
rs62325485 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LNX1 | GRCh38.p7 | 4:53610138 | GTTTTTCATATGTCC[A/G/T]CAGAACATTTATAGA | 84708 |
rs62325486 | snp | C/T | 0.479014 | 0.100263 | intron-variant | LNX1 | GRCh38.p7 | 4:53613048 | GTGTATGTCTACCTA[C/T]GATTATATAGCCATG | 84708 |
rs62325487 | snp | A/G | 0.478932 | 0.10045 | intron-variant | LNX1 | GRCh38.p7 | 4:53613252 | CCCATGCATGCATTT[A/G]TGAAAATATATGAAT | 84708 |
rs62325488 | snp | A/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53613345 | CTCCTGCTTTCCAGG[A/T]ATTTTTTTTTTTTAA | 84708 |
rs62325489 | snp | C/T | 0.47885 | 0.100637 | intron-variant | LNX1 | GRCh38.p7 | 4:53613497 | GTTATTTTTCCTGAT[C/T]CTCTCCGTCCTCCAC | 84708 |
rs62325509 | snp | G/T | | | intron-variant | LNX1 | GRCh38.p7 | 4:53621085 | TACTCAGAGTGTGGT[G/T]CACAGGGCACGGTGA | 84708 |
rs62325510 | snp | C/G | 0.0858192 | 0.188533 | intron-variant | LNX1 | GRCh38.p7 | 4:53640617 | CCAGTTGCAGGAGAA[C/G]CACAATACATCCATA | 84708 |