| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs8048 | snp | C/T | 0.462691 | 0.131387 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732949 | TCATGGAATCCACTG[C/T]TATGCAGCCACACTG | 7805 |
| rs8056 | snp | A/C | 0.0349115 | 0.127424 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732942 | GCTGCATAACAGTGG[A/C]TTCCATGAAAGGAGT | 7805 |
| rs9146 | snp | A/G | 0.11963 | 0.213316 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732548 | GAGAAGGCTCTGCAA[A/G]AGCTCCCTGGCAATA | 7805 |
| rs1050663 | snp | A/G | 0.494598 | 0.051691 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742517 | GTTCATCGAGCACTC[A/G]GTAGAGGTGGCCCAT | 7805 |
| rs1050731 | snp | A/G | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732616 | CAGGGAGCTGACCCA[A/G]AGGTGGAGGCCACGG | 7805 |
| rs1050732 | snp | A/C | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732604 | CCAGAGGTGGAGGCC[A/C]CGGAGGCAGGGTCTC | 7805 |
| rs1050733 | snp | C/T | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732589 | ACGGAGGCAGGGTCT[C/T]TGGGGACTGTCGGGG | 7805 |
| rs1050739 | snp | A/G | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732567 | CTGTCGGGGGGTACA[A/G]AGGGAGAAGGCTCTG | 7805 |
| rs1050746 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732561 | GGGGGTACAGAGGGA[A/G]AAGGCTCTGCAAGAG | 7805 |
| rs1050748 | snp | C/T | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732554 | CAGAGGGAGAAGGCT[C/T]TGCAAGAGCTCCCTG | 7805 |
| rs1050752 | snp | A/T | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732534 | AGAGCTCCCTGGCAA[A/T]ACCCCCTTGTGTAAT | 7805 |
| rs1078609 | snp | A/G | 0.207864 | 0.246424 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740727 | TAGCTGAACCCTTTG[A/G]GTTTCTGCACAAGCA | 7805 |
| rs1078610 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740761 | ACAGCCACCCTGCAC[A/C]AGGCAAACGGCCTCC | 7805 |
| rs1188346 | snp | A/T | 0.470811 | 0.117228 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753528 | ttttctcatgattag[A/T]ctgggaatgtgcttt | 7805 |
| rs1188347 | snp | A/G | 0.470715 | 0.117409 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753493 | aggaagaccacagag[A/G]tgatgtgccagtctc | 7805 |
| rs1188348 | snp | A/G | 0.452103 | 0.147154 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751153 | CCCATGGCCCATCCC[A/G]CCCAGAGAGTGGCTG | 7805 |
| rs1188349 | snp | C/T | 0.325327 | 0.238382 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750810 | TACCATTTGTGGCAC[C/T]GGAAAAATGGCAGCT | 7805 |
| rs1188350 | snp | C/T | 0.490673 | 0.0676508 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749469 | tgtataatttaccta[C/T]agaaaagcacagcta | 7805 |
| rs1188351 | snp | C/T | 0.279461 | 0.248258 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749071 | ccagcttggggctgt[C/T]acaaataaggcagcc | 7805 |
| rs1188352 | snp | A/G | 0.200492 | 0.245049 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746442 | CTTGGAGGCTTGGAA[A/G]TGTTGACTGTCTGCA | 7805 |
| rs1188353 | snp | G/T | 0.189576 | 0.242588 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745432 | AGGGGAGGGAGGGGG[G/T]ACTGCAGAGGGAGAG | 7805 |
| rs1188355 | snp | A/G | 0.283421 | 0.247756 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737820 | CAGCGTGGCACAGCC[A/G]TCACCTTGGTCGACC | 7805 |
| rs1188356 | snp | G/T | 0.306927 | 0.243432 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738235 | gctggacttagcaac[G/T]cacttctaactaaca | 7805 |
| rs1188357 | snp | G/T | 0.435119 | 0.16802 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738435 | tgagccaccaggagt[G/T]catccttcagatcta | 7805 |
| rs1188358 | snp | A/C | 0.304438 | 0.244001 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739394 | AGCCCTCAAGCCACC[A/C]CACAGTGGGCGCTCA | 7805 |
| rs1188359 | snp | A/C | 0.309154 | 0.242901 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739467 | CAAAGAAGAAATAAT[A/C]CTGGGGGCTGGGGGC | 7805 |
| rs1188360 | snp | A/G | 0.496649 | 0.0407971 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739529 | CAATTCACTCCCAGC[A/G]GCACTGACTGAGTGC | 7805 |
| rs1323444 | snp | A/C | 0.0240643 | 0.107019 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759229 | CACTGCACTGTGTCA[A/C]CTTTCTATGATGTCA | 7805 |
| rs1323445 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747442 | GGCTGGGACCGCAGC[C/T]TGAGCCTGGCTTGGA | 7805 |
| rs1407881 | snp | C/T | 0.152001 | 0.229992 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759429 | TAGGAAATCGTCAAA[C/T]GGCTTCTGTGCACAA | 7805 |
| rs1407882 | snp | A/G | 0.423413 | 0.180077 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757348 | ATGGGGCACAGCAGC[A/G]GCCGGAAGGTTATTT | 7805 |
| rs1407883 | snp | A/G | 0.425894 | 0.177655 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757279 | AGGCAGGGATCTTGG[A/G]AGGAACGTGGGCTGG | 7805 |
| rs1407884 | snp | C/T | 0.285519 | 0.247464 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757252 | CTGGGATTGTTTGAC[C/T]GGGATGTGAGGTCGG | 7805 |
| rs1407885 | snp | C/T | 0.398174 | 0.201356 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757036 | CATTAGGGTAACTTG[C/T]CCGGCCCAAGCTCTT | 7805 |
| rs1407886 | snp | A/C | 0 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754963 | CTGGCAACAGGTGTG[A/C]TGATAGGACCTTGAG | 7805 |
| rs1535637 | snp | A/G | 0.144969 | 0.226867 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735055 | ATGAGGGTTGGAACA[A/G]AAGAAATGTGTTCTC | 7805 |
| rs1590340 | snp | C/G | 0.43598 | 0.167067 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738008 | agccaaaatgatctt[C/G]tagagaagagcatag | 7805 |
| rs1614931 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753835 | ggcctagttcctcta[G/T]tgctaacgtctcaac | 7805 |
| rs1623695 | snp | C/T | 0.306679 | 0.24349 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738005 | CACCTATGCTCTTCT[C/T]TACAAGATCATTTTG | 7805 |
| rs1746056 | snp | A/G | 0.497829 | 0.0328757 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752875 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 7805 |
| rs1804623 | snp | G/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733071 | AACAATTAGCTCCAG[G/T]AAATAACAGTTATTT | 7805 |
| rs1853449 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743824 | AGTTGAGACCTGTGT[C/T]TGAGCTAAAAAAAAA | 7805 |
| rs1882024 | snp | C/T | 0.439224 | 0.163383 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746868 | TGCACCTGCTGTGTG[C/T]CCGGCTCCGCGCACC | 7805 |
| rs1920420 | snp | G/T | 0.420255 | 0.183066 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749644 | CTGAGCTCTGGGTGT[G/T]GACCCAGAGCCCTGT | 7805 |
| rs1951782 | snp | A/G | 0.475789 | 0.107327 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754594 | ATTCTTTTTTTCAAA[A/G]TTCAGTAACTTGCCC | 7805 |
| rs2178424 | snp | A/C/G | 0.163236 | 0.234461 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736537 | CTCCCAGGCTCAAGC[A/C/G]ATCCTCCCGCTTCAG | 7805 |
| rs2273979 | snp | A/G | 0.384017 | 0.211044 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757821 | GGAGGGCAGCCAGCA[A/G]CTTCCCCTTCTCTGC | 7805 |
| rs2377488 | snp | C/G | 0.28578 | 0.247426 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757160 | GAGGCACAAAGGGGA[C/G]ATCCCCACTTCTCAT | 7805 |
| rs3748602 | snp | G/T | 0.141258 | 0.225111 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741522 | GAAGATCTCCAGAAC[G/T]CAGGTGGGACCGCCT | 7805 |
| rs3748603 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742124 | GCAGAGGCTGGATCC[C/T]ATGGTGAGGAGTTTC | 7805 |
| rs3762295 | snp | C/T | 0.0648419 | 0.167978 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758538 | GGCTCCAGACAAGGA[C/T]GGAAGAATAACCAGG | 7805 |
| rs3762296 | snp | A/G | 0.497613 | 0.0344622 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758539 | GCTCCAGACAAGGAC[A/G]GAAGAATAACCAGGA | 7805 |
| rs3762297 | snp | C/T | 0.384209 | 0.210922 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758833 | AGGGAATAGGAAGTA[C/T]ATGCAACATTTCTGG | 7805 |
| rs3790495 | snp | C/T | 0.0916144 | 0.193427 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748668 | CCAGATACCACCAGA[C/T]GCCCCCATTCCTGGG | 7805 |
| rs3790496 | snp | A/T | 0.432063 | 0.171327 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749144 | TTGTGGTAGATTCAT[A/T]CAATGGAGTATACAC | 7805 |
| rs3790497 | snp | G/T | 0.255224 | 0.249945 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749323 | ATAGACAGGCAGAAG[G/T]CAGTGGGGGCGGGGC | 7805 |
| rs3790500 | snp | A/C | 0.130694 | 0.219696 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749682 | CCGTAGGGGTCAGGG[A/C]GGGCTTCTCAGAGGA | 7805 |
| rs3790501 | snp | C/T | 0.125528 | 0.21681 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749782 | GCAGAGGCCAGTGTG[C/T]ATGAGACGCATTCAG | 7805 |
| rs3790502 | snp | G/T | 0.155656 | 0.231515 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755931 | CAAGCAAGGGCTCCC[G/T]GGGTCACCGCAGGCC | 7805 |
| rs3790503 | snp | A/G | 0.372189 | 0.218105 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756228 | ACAGGGTACAGGGAC[A/G]CTCAAAGAGTGATTT | 7805 |
| rs3795437 | snp | A/G | 0.433655 | 0.16962 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733959 | TTGGAATTGCAGGTC[A/G]TTCTTGACCATACTC | 7805 |
| rs3795438 | snp | A/G | 0.345418 | 0.231074 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733790 | GTGCTGGGAGGGGTG[A/G]AGCTGCCTCATAATC | 7805 |
| rs3795439 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732843 | AGTCATAGGCGAATC[G/T]GTTCTGCCCGAGGCT | 7805 |
| rs3828053 | snp | A/T | 0.348574 | 0.229746 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750504 | CACTCTCTCGTGTCA[A/T]CCTCGCGCCAGTCTT | 7805 |
| rs3833525 | in-del | -/AG | 0.0142054 | 0.0830717 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741767 | TGCCCCTGGGACCCC[-/AG]CCAGGCTCCCAGGAC | 7805 |
| rs3833526 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742216 | CCTTTACCAGCTGGT[-/G]GGGATTTGCAAAGTG | 7805 |
| rs4319383 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754101 | TGACAGTGGAATTCC[A/G]GGCACTCTGGGGAAG | 7805 |
| rs4409706 | snp | A/G | 0.436976 | 0.165952 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751689 | GGTTGCAGTGAGCCA[A/G]GATCACGCCACTGCA | 7805 |
| rs4614309 | snp | G/T | 0.489665 | 0.0711382 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758407 | TGAAGGTGCAAGGAT[G/T]TTAACTGAGGCTGAC | 7805 |
| rs5773314 | in-del | -/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742762 | CTCTCTCCAGCTATG[-/T]GACCCTGGGCAAGCT | 7805 |
| rs6671857 | snp | G/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758964 | TCATGGAGTTAGGAT[G/T]GGACACTGCTGCAGC | 7805 |
| rs6684975 | snp | A/G | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733290 | TCTAAATGACTCATG[A/G]TTGGCTAATTGATTA | 7805 |
| rs6685063 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755091 | GGACCACAGCCTGGA[C/G]ACAACCTGGGCCGAG | 7805 |
| rs6685295 | snp | C/G | 0.286825 | 0.247273 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755351 | ATGAAGAATTATCCA[C/G]CCCAAAATATCAATG | 7805 |
| rs6702831 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752799 | CTCCTTCTTCAAATA[C/T]TATGATTTGAATGCT | 7805 |
| rs7415292 | snp | G/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732315 | tgtggggggagtgtg[G/T]gtgtttgggtgtatt | 7805 |
| rs7416874 | snp | C/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732184 | GTGTGTGGgggtggg[C/G]gtgtgtggaggggtg | 7805 |
| rs7417219 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737943 | tgcttcccaggctgg[C/T]gcaccggcccatccc | 7805 |
| rs7417251 | snp | A/C | 0 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738083 | ctcccctaggggcag[A/C]ttgaaaccaatgact | 7805 |
| rs7512767 | snp | A/G | 0.181022 | 0.240296 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750546 | TCTAACATGAGTCCC[A/G]TATTTTTCTGATTTT | 7805 |
| rs7514358 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755863 | CGGCCACCAGGGCCC[A/G]CAATCCTTCGTGGCA | 7805 |
| rs7549164 | snp | C/T | 0.424503 | 0.179021 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751346 | TCCAGCCCAGGGGCA[C/T]TGGACATAAAGGTGG | 7805 |
| rs10914189 | snp | C/T | 0.410568 | 0.191619 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734934 | TGGCATCTTAGTTTT[C/T]TCTGCGCCTCCTGGA | 7805 |
| rs10914190 | snp | C/T | 0.448195 | 0.152377 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736949 | ttgagtcctctattt[C/T]ccatgctgaataaac | 7805 |
| rs10914192 | snp | G/T | 0.0422008 | 0.138995 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750602 | TACACATGGGCTCTG[G/T]GCTTCTCAGAACAAG | 7805 |
| rs10914193 | snp | A/G | 0.497586 | 0.0346604 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758486 | CCTGAGCCGCAGGGA[A/G]AAGCTTGTTCTTCCT | 7805 |
| rs11541205 | snp | A/G | 0.0217236 | 0.101931 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733215 | TTAAATGGTTTGGAG[A/G]CTAACGTGATTTTTT | 7805 |
| rs11541206 | snp | C/G | 1.65701e-05 | 0.00287833 | missense | LAPTM5 | GRCh38.p7 | 1:30737604 | TGTCCTTATCTTCAA[C/G]GTGAGTGGATCCCTG | 7805 |
| rs11585511 | snp | A/G | 0.21845 | 0.248001 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744122 | CTGGGGCAAGCTTAC[A/G]TGGTTCGGCAGTAGT | 7805 |
| rs11586021 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745018 | CATGAGGTCACCTTG[A/G]ACATTACCCGACTTT | 7805 |
| rs11586791 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739731 | GCCTGAGCACAGGGC[C/T]CGTGTCTGGTCCCCT | 7805 |
| rs11801629 | snp | C/G | 0.398534 | 0.201091 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758279 | TGGATTCACTCCTTT[C/G]ATCCTCACCTCAATC | 7805 |
| rs11808067 | snp | A/T | 0.0232847 | 0.105357 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759023 | AGAAAGTCCCTAAGC[A/T]CCTCCCACTTGGCAG | 7805 |
| rs12032350 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732356 | tgggggtgggtgTGA[A/G]TGTGTGGAGGGGTGT | 7805 |
| rs12077548 | snp | A/G | 0.0275645 | 0.114116 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749291 | taattctacagatgt[A/G]tgtattatagaacta | 7805 |
| rs12078167 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741023 | GGTTCCTCTTCTGCA[A/G]GGGATTGAGCTACAG | 7805 |
| rs12078854 | snp | A/G | 0.231189 | 0.249291 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750010 | AGAACCTAGACTCGG[A/G]CGGCTCAGATGGCGC | 7805 |
| rs12079273 | snp | A/G | 0.216349 | 0.247725 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745004 | TGTCCTCCTGAGGCC[A/G]TGAGGTCACCTTGGA | 7805 |
| rs12083195 | snp | A/G | 0.122411 | 0.214991 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752801 | CCTTCTTCAAATACT[A/G]TGATTTGAATGCTTT | 7805 |
| rs12085079 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751225 | GAGGAGAACAACTCA[A/G]TTCTGACACTGAGGA | 7805 |
| rs12086854 | snp | A/G | 0.0543475 | 0.155628 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746858 | gGAATCGTGTGGTGC[A/G]CGGAGCCGGGCACAC | 7805 |
| rs12096207 | snp | C/G/T | 0.0555004 | 0.157171 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746641 | CTTGCTCCCCAATTA[C/G/T]AGCATCTTTTCACCC | 7805 |
| rs12117692 | snp | C/T | 0.287346 | 0.247195 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754408 | GGCCATGGTGGCATG[C/T]GCCTGTGATCCTAGC | 7805 |
| rs12137058 | snp | G/T | 0.293807 | 0.246132 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754180 | GTCCACTTTCTACCA[G/T]CGACTTAGAACGTGC | 7805 |
| rs12240197 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751232 | ACAACTCAGTTCTGA[C/T]ACTGAGGAGGGGCTA | 7805 |
| rs12404920 | snp | C/T | 0.459574 | 0.136304 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734110 | CCTGTAGTGGACATA[C/T]TTGCCTTTGCCTATT | 7805 |
| rs12405718 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737365 | ATTCCAGACAGCTGG[A/C]ATTAGACATCTGAAC | 7805 |
| rs12744988 | snp | C/T | 0.339429 | 0.233457 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757163 | GCACAAAGGGGAGAT[C/T]CCCACTTCTCATCCC | 7805 |
| rs12754344 | snp | C/T | 0.4582 | 0.138394 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741973 | CAGCCAGGGTGAGGC[C/T]GAGGAAGGCATCCCT | 7805 |
| rs13375440 | snp | A/G | 0.0663309 | 0.169604 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746222 | TTTTCCCCTGGGGCC[A/G]TTGGGATGACAGAAC | 7805 |
| rs16834046 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750740 | AACACAGGCTGCAGA[A/G]TCACTTGCCCTCCTG | 7805 |
| rs16834049 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751094 | GGAGGCCTCGGGGCC[A/G]GGTTGGCAACAGAGA | 7805 |
| rs16834054 | snp | C/G | 0.0678174 | 0.1712 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752454 | TTGACAAACCTGCTA[C/G]GTCTCTGAAGCACTG | 7805 |
| rs28362505 | in-del | -/C | 0 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733355 | TTAATTAGTTACCCC[-/C]TATATATAAATATAT | 7805 |
| rs34101571 | snp | C/T | 0.0243598 | 0.107641 | missense, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739047 | AGCTCCTCCAAGTTC[C/T]CCCTGATGACGCTGC | 7805 |
| rs34342174 | in-del | -/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748616 | GGGGGCCAGCCCCCC[-/C]AAGAGCACTATCTCC | 7805 |
| rs34359099 | in-del | -/A | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737705 | GAGGTAATTCTGCAA[-/A]CAGATTTGGGGGCCA | 7805 |
| rs34427039 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754221 | AAAAAGCCAGGACCC[-/C]AAGAGACCCAATTTA | 7805 |
| rs34854980 | snp | A/T | 0.29432 | 0.24604 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752831 | TACCTTTTTTTTTTT[A/T]AAAGAGTCTCACTCT | 7805 |
| rs34923956 | in-del | -/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735131 | CCAAATGGCACAGGG[-/G]AGTTAGTGACAGGGC | 7805 |
| rs35351292 | snp | A/G | 0.31751 | 0.240712 | missense | LAPTM5 | GRCh38.p7 | 1:30735195 | CGGTGGAGGAGAAGA[A/G]AAACTCCAAGATGCT | 7805 |
| rs35391929 | snp | C/T | 0.0441095 | 0.141807 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759512 | GGTGCAAAGCCAACT[C/T]CCAAAGAGAGGGATG | 7805 |
| rs35702385 | in-del | -/T | 0.399432 | 0.200425 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752819 | ACCTTTTTTTTTTTT[-/T]AAAGAGTCTCACTCT | 7805 |
| rs35736676 | in-del | -/T | 0.480775 | 0.0961398 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753085 | TACTTTTTTTTTTTT[-/T]CCAATTTAAAAGTAG | 7805 |
| rs35757328 | in-del | -/A | 0.403509 | 0.197319 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751738 | CAGTCTCAAAAAAAA[-/A]GGGGCGGGGGGCCTT | 7805 |
| rs35787459 | snp | A/C | 0.0317378 | 0.121908 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739877 | GACTATCTCCTGTGC[A/C]TGCTCACCCTGCTGG | 7805 |
| rs35799087 | in-del | -/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734402 | AGGGGTTTTGGCAGC[-/G]CTTTTTGCCACCACA | 7805 |
| rs35831416 | in-del | -/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749675 | GGTCCAACCGTAGGG[-/G]TCAGGGCGGGCTTCT | 7805 |
| rs35861621 | in-del | -/C | | | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757796 | GAAAGAGCCTGGTGC[-/C]TGGAGCAGGGCAGAG | 7805 |
| rs35997261 | snp | A/C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755156 | CTTGCTCCTGCTCTA[A/C/G]AACGTCTCATCACTC | 7805 |
| rs45527142 | snp | A/G | 0.00104767 | 0.0228634 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741615 | CAGGAAGGGGCAGGG[A/G]GCAGCGGGGCTCCTG | 7805 |
| rs55748171 | snp | G/T | 0.300421 | 0.244863 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734409 | TTTGGCAGCCTTTTT[G/T]CCACCACAAGGGATG | 7805 |
| rs55928433 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751770 | GGGCCTTGTGTTCTT[C/T]TTCCACAGCCCACTT | 7805 |
| rs56126824 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755799 | AGCATTGAAACATCA[A/G]AAGATGTGACACAAA | 7805 |
| rs56296001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737809 | ACACACGAGCACAGC[A/G]TGGCACAGCCGTCAC | 7805 |
| rs56341536 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743905 | CGGAAGAGTGATGAA[A/G]AGCTGGGCTCCAGAA | 7805 |
| rs59992159 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734324 | GCCCAAGTTGGTCCA[A/G]TCAGACATACTCCTG | 7805 |
| rs61767294 | snp | C/T | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743586 | AAGCCCTCCACCCTT[C/T]CCCTATGACATACAT | 7805 |
| rs61767295 | snp | C/T | 0.160609 | 0.233472 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749470 | AGCTGTGCTTTTCTA[C/T]AGGTAAATTATACAT | 7805 |
| rs72654974 | snp | A/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757191 | CCCCTCGAGTGGCCC[A/T]GGCTCCCTCCAGGCC | 7805 |
| rs72876490 | snp | A/G | 0.00112172 | 0.0236559 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735148 | GTTAGTGACAGGGCT[A/G]GCACCCACCTGCAGC | 7805 |
| rs72876496 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748219 | GGACACTTTCCTATC[C/T]GTTTACTTCATTGGC | 7805 |
| rs74063208 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739491 | TGGGGGCTAAAAAGC[A/G]CACATGTCCTTTCCT | 7805 |
| rs74063214 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753412 | AGTAACCTCAGCCGG[A/G]GGCTCAAAGTCACCA | 7805 |
| rs74063217 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755315 | CTGAACTTCCTCTAA[C/T]GCACAATTCACTCCC | 7805 |
| rs74063222 | snp | C/T | 0.0310518 | 0.120672 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758883 | CACAGCTGAGCCCCT[C/T]TGCAATGCCAAGCTT | 7805 |
| rs74063223 | snp | C/T | 0.0279526 | 0.114869 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759649 | AACTAGTCCATGAAT[C/T]CTGTGATTTTCCATT | 7805 |
| rs74842333 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747372 | GAGACAGCGACCAGC[A/C]CAAGGTCACACACCA | 7805 |
| rs74897727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743618 | CAGTTCTCCAGGTAA[A/C]CTCTGCCCATATAAA | 7805 |
| rs74977890 | snp | C/T | 0.0357611 | 0.128848 | missense | LAPTM5 | GRCh38.p7 | 1:30757685 | TGGCCAGGGCGGTGG[C/T]TGCGATGCGGACATT | 7805 |
| rs75102360 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732432 | GCTGGTCTCCACCCT[C/T]CCTACACTGTATTTC | 7805 |
| rs75149979 | snp | G/T | 0.0287284 | 0.116357 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739459 | CTTGGTTCCAAAGAA[G/T]AAATAATACTGGGGG | 7805 |
| rs75190698 | snp | A/C | 0.109861 | 0.207029 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753074 | GGCATGAGCCACCGC[A/C]CCTGGCCGTACTTTT | 7805 |
| rs75325028 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736069 | AGGGGAGCTGGGGGA[C/T]GGAGCTGTGTGCTGG | 7805 |
| rs75394921 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748070 | GCCCACTCTCTCTCA[C/G]TCCCTGAGGCCCAGG | 7805 |
| rs75713938 | snp | C/G | 0.0603597 | 0.1629 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751998 | CCCCAAAGTGGAGCA[C/G]AGAAAAGAGCCCCAG | 7805 |
| rs75819954 | snp | A/G | 0.0283406 | 0.115616 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749314 | TAGAACTACATAGAC[A/G]GGCAGAAGTCAGTGG | 7805 |
| rs75995270 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755514 | CCTCACCTTCCATAC[G/T]GCCCACAACCAAACT | 7805 |
| rs76130151 | snp | A/G/T | 0.0444908 | 0.142359 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736993 | TTGGGTTTTGTGGGG[A/G/T]TTTTTTGACTTCCTA | 7805 |
| rs76311239 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748857 | GAACCCCAGTGCAGC[C/T]GCTGATCCCCTGTGG | 7805 |
| rs76444650 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749187 | AATGAGTTAGCTACC[C/T]GCAACCACACAGACG | 7805 |
| rs76524516 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738409 | TAGGCAAAGAGCCCA[C/T]GCCCTGTGAGTGAGC | 7805 |
| rs76835809 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746865 | TGTGGTGCGCGGAGC[C/T]GGGCACACAGCAGGT | 7805 |
| rs76884088 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739404 | CCACCCCACAGTGGG[C/T]GCTCACTGGCATGAA | 7805 |
| rs76914164 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752835 | TTTTTTTTTTTTAAA[G/T]AGTCTCACTCTGTCA | 7805 |
| rs76985979 | snp | A/G | 0.0433465 | 0.140692 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743536 | TTCCAGCCATGGGGA[A/G]CTCACAACCTTATGT | 7805 |
| rs77122854 | snp | A/C | 0.194278 | 0.243711 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738542 | CCAGCTAAGCCACTC[A/C]CAAGCTCCTGATCCT | 7805 |
| rs77190466 | snp | C/T | 0.0225045 | 0.103662 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749253 | TCACAAAAGAACACG[C/T]GCTGCAGAATTTCAT | 7805 |
| rs77278616 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735580 | CTGGAAGCTCACTAC[C/T]TCCTGAGACAGCCCT | 7805 |
| rs77510939 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744495 | GGCTTAGAGAAGGAC[C/G]ATGAGCATCTGCCAG | 7805 |
| rs77548113 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748152 | GGGAGGTAAAGGTTA[C/T]AGAGAAAGGACCCAG | 7805 |
| rs77578501 | snp | C/G/T | 0.0333954 | 0.124982 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748372 | CCCTTGCCCCTCCCC[C/G/T]TCAGGGCTGCTCCAC | 7805 |
| rs77631014 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743111 | CTCTGTCTCCCATGG[C/T]CCCTCAGGGAACAAT | 7805 |
| rs77720776 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741007 | GGACCCAGGGACCGC[A/G]GGTTCCTCTTCTGCA | 7805 |
| rs77736166 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734655 | GTGAGGAAAGTAAGT[A/T]ACCAGGAATTTAAAC | 7805 |
| rs77970901 | snp | A/C | 0.0524604 | 0.153226 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752424 | ACACCTCGTGGCCAC[A/C]CCTCCTAACCCAGCT | 7805 |
| rs78423254 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737264 | ACTCCTGCCCCTGAG[A/G]CCCAGAGAGAAGTGA | 7805 |
| rs78577389 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738364 | GAGAGCACTCAAGCA[A/G]CACTACTACAAGTCC | 7805 |
| rs78602554 | snp | A/G | 0 | 0 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752834 | CTTTTTTTTTTTTAA[A/G]GAGTCTCACTCTGTC | 7805 |
| rs78665369 | snp | G/T | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742952 | CTTAAAGAGGTGGGG[G/T]GGGGGGTAGAAGCTG | 7805 |
| rs79160371 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752561 | AAAGCCCTACTCATC[C/T]TTAAGACTCAGACCT | 7805 |
| rs79191826 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749911 | AACACACGGATCCAC[C/T]GGTTTGGCAGGGGTG | 7805 |
| rs79243755 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743704 | CCCTAAGTTTACATC[A/G]GCTTTCTAGGCAGCC | 7805 |
| rs79297199 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733510 | TGAACTGATCAAGTC[A/G]ATAGTTGCTTGACAA | 7805 |
| rs79835875 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747663 | TCTGAGGAGCAAGCA[A/G]CAGGTTGAGCTAAAA | 7805 |
| rs79990487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750011 | GAACCTAGACTCGGA[C/T]GGCTCAGATGGCGCT | 7805 |
| rs80054126 | snp | G/T | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737000 | TTGTGGGGGTTTTTT[G/T]ACTTCCTAAGATGGC | 7805 |
| rs111241633 | in-del | -/GTGT | 0.5 | 0 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732374 | TGTGGAGGGGTGTGG[-/GTGT]AGGGGGTGTGGGTGA | 7805 |
| rs111341804 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752543 | TTTCCAAGGTGCCCA[A/G]GCAAAGCCCTACTCA | 7805 |
| rs111344639 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750383 | CGCCAGGTCCTCTTC[A/T]GAACTTATACAGTCG | 7805 |
| rs111347292 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732278 | TGTGGAGGGGTGTGG[A/G]GAGGGTGTGAGTGTG | 7805 |
| rs111451929 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758311 | TTTGAGAGAGGTACT[A/G]TTATGATCCCCATTT | 7805 |
| rs111455721 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739327 | CTTCAAGGACAACAG[C/T]TGGGGAGAGTGAGAA | 7805 |
| rs111495917 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751549 | TTCAAGACCAGCCTG[G/T]CCAACATGGTGAAAC | 7805 |
| rs111589481 | snp | C/T | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738035 | GGCTGACAGGGACCA[C/T]CTAATCCACTAATAC | 7805 |
| rs111672854 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732279 | GTGGAGGGGTGTGGG[A/G]AGGGTGTGAGTGTGT | 7805 |
| rs111682374 | snp | A/G | 0 | 0 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732349 | GGGTGTGTGGGGGTG[A/G]GTGTGAGTGTGTGGA | 7805 |
| rs111762806 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747808 | GTGCACCAGGTGTCA[C/G]CTGGGAGGCACTGGC | 7805 |
| rs111910857 | snp | A/G | 0 | 0 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757947 | GCCTCAGAGCACCCC[A/G]CTGCCCTCTGCCATT | 7805 |
| rs111914912 | snp | C/G | 0.0345262 | 0.126772 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753534 | CATTCCCAGACTAAT[C/G]ATGAGAAAACCACCA | 7805 |
| rs111952312 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737345 | CGCAGGCCAGTCCAA[A/G]TCTAATTCCAGACAG | 7805 |
| rs111974206 | snp | C/G/T | 0 | 0 | splice-donor-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739808 | GGGGCTGGGTACTCA[C/G/T]AGCACGGCTCCGGGA | 7805 |
| rs111985890 | snp | C/G/T | 0 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737702 | TGGGGAGGTAATTCT[C/G/T]CAACAGATTTGGGGG | 7805 |
| rs112292903 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754078 | TTTTAACCCAGACAA[C/T]GCATTTCTGACAGTG | 7805 |
| rs112374342 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739075 | GCTCTGGGGAGGACA[A/G]ATACAAGGAGGAGGA | 7805 |
| rs112626544 | snp | C/T | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735153 | TGACAGGGCTGGCAC[C/T]CACCTGCAGCCACAC | 7805 |
| rs112789896 | snp | A/G | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756371 | GGTGCCATGTCTGAT[A/G]CACAACGAATAATAA | 7805 |
| rs112803264 | snp | C/T | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741783 | GCCAGGCTCCCAGGA[C/T]CACACTTGGGGAACC | 7805 |
| rs112874896 | in-del | -/AGAGAA | 0.5 | 0 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744361 | GTTTCACCTTGAACG[-/AGAGAA]AGAGAAAGGGAGGCA | 7805 |
| rs112912738 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757460 | CCTCACTCTTGCGGC[A/G]TCTCCCCAGGGTACC | 7805 |
| rs113052491 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733655 | CGTTGACCCAGTTGT[C/G]AGCAGCTCACAGGCC | 7805 |
| rs113208828 | snp | A/C | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757250 | GGCCGACCTCACATC[A/C]CGGTCAAACAATCCC | 7805 |
| rs113304071 | snp | C/G/T | 0.000393937 | 0.01403 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739958 | AGGTAGGCCCAGCAC[C/G/T]GTCAAGTGTCCCCTG | 7805 |
| rs113336710 | snp | C/T | 0.00154139 | 0.0277185 | missense | LAPTM5 | GRCh38.p7 | 1:30733872 | GGCCCCCCTCTGGGG[C/T]CTTCGATGGCAAAGA | 7805 |
| rs113373509 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732429 | AAGGCTGGTCTCCAC[C/T]CTCCCTACACTGTAT | 7805 |
| rs113411400 | snp | A/C/T | 0.000891299 | 0.0210951 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757633 | ACAAGCACGCACGCA[A/C/T]ACACACCCGGGGCCC | 7805 |
| rs113467904 | snp | C/G | 0 | 0 | splice-donor-variant, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742455 | CGTCCCCTGGACCTA[C/G]CGATCCTGAGGTAGC | 7805 |
| rs113531450 | snp | C/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733059 | TGTTTTATGATGAAA[C/T]AACTGTTATTTCCTG | 7805 |
| rs113535532 | snp | A/G | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739307 | ATGATGTAGCCCCCC[A/G]GTCTCTTCAAGGACA | 7805 |
| rs113677939 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749741 | GAGCAATGGAAAAAG[C/T]GTTCCAGGCAGAGGA | 7805 |
| rs113728727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746860 | AATCGTGTGGTGCGC[A/G]GAGCCGGGCACACAG | 7805 |
| rs113764694 | snp | C/T | 0.5 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737955 | TGGCGCACCGGCCCA[C/T]CCCCAGCTGGCAGGT | 7805 |
| rs114057694 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742687 | CAGGTCAGTAGGGCA[A/T]CTCAGACAAAAGAGT | 7805 |
| rs114082244 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737910 | CAAGAAAAGCCAAGT[A/G]GCTACTATCTCCAGA | 7805 |
| rs114196191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752494 | TCCCCTCCAAGCCTG[C/T]GTCATGCTACTCCCC | 7805 |
| rs114463600 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735936 | AGACATATGGAGGTA[C/T]GGAGTGACAAAGAAT | 7805 |
| rs114504145 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755200 | CTCAACTGGGAGAGA[C/T]TGGGCCCCATAACTA | 7805 |
| rs114662190 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745697 | GACCTTCCACGAAGA[C/T]GCCAGGCCCTGACCC | 7805 |
| rs114678198 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750529 | AGTCTTGAGAGACAG[C/G]TTCTAACATGAGTCC | 7805 |
| rs114873698 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755657 | GGACATCGGATGGCA[C/T]GATCAACAAGAAACC | 7805 |
| rs115008385 | snp | A/G | 0.0486741 | 0.148216 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752837 | TTTTTTTTTTAAAGA[A/G]TCTCACTCTGTCAGG | 7805 |
| rs115025460 | snp | A/G | 0.0441095 | 0.141807 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749675 | GGTCCAACCGTAGGG[A/G]TCAGGGCGGGCTTCT | 7805 |
| rs115204426 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749349 | GGGGCAGTGGCGAGG[C/T]GGGGGCTCTAGGGGC | 7805 |
| rs115211698 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737353 | AGTCCAAATCTAATT[A/C]CAGACAGCTGGAATT | 7805 |
| rs115320346 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745761 | CCCATGTGGCTCTCT[A/G]GGACATAGGATGGAG | 7805 |
| rs115524147 | snp | A/G | 0.0150606 | 0.0854603 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732783 | TGGGTTTAGTCCAAC[A/G]AACAGATGTGCCTGA | 7805 |
| rs115594638 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750142 | GATATTCTGGCTGGT[A/G]GTAGCTTATCAAATC | 7805 |
| rs115707811 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752151 | CCACCCCAGCCATGG[A/G]GCAGGGAAGGAACTC | 7805 |
| rs115805953 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753409 | AGGAGTAACCTCAGC[C/T]GGGGGCTCAAAGTCA | 7805 |
| rs115865477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749927 | GGTTTGGCAGGGGTG[A/G]GGCCTCTGGGGTTAG | 7805 |
| rs116073027 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756722 | TTTGCAGCAACCCAC[C/T]GCAGCATGTGGATCT | 7805 |
| rs116077605 | snp | A/G | 0.0314385 | 0.121371 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750422 | TATCACGGGCTCTGC[A/G]TCTGAGTATTTTCAA | 7805 |
| rs116158021 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744612 | TCCCCTTGCTAGAAG[C/G]AGCCTGCATGTACTT | 7805 |
| rs116352948 | snp | A/G/T | 0.0258754 | 0.110766 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735315 | GAGCGTCCTTCTCAC[A/G/T]CTCCAGCAGGCCTAG | 7805 |
| rs116468789 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745164 | GCCTAACTCCATGCC[A/G]CATGATCTTCCCCAC | 7805 |
| rs116773819 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742037 | TGAGACAGGGACAGG[A/G]TTGGTGAGGTCAGTG | 7805 |
| rs116775265 | snp | C/T | 0.0150606 | 0.0854603 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732439 | TCCACCCTCCCTACA[C/T]TGTATTTCCAGAAAC | 7805 |
| rs116992015 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745589 | TTTGTCCCCATTGCC[A/G]GATGGCTCACGAGAC | 7805 |
| rs117174760 | snp | A/G | 0.0197687 | 0.0974348 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732715 | ACCGCCATGACCCCA[A/G]TGGCAGGGTCAGTGC | 7805 |
| rs117463791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754995 | TAGCCTATGGGAAAG[C/T]CCCCAGGCCCTGCCC | 7805 |
| rs117989491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753271 | TAATTTATGTAGCTA[C/T]TCTGCCCTCAAGGAG | 7805 |
| rs138003202 | snp | A/G | 7.06914e-05 | 0.0059448 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742537 | GCTCGATGAACAACA[A/G]GACGCTCATGATCTG | 7805 |
| rs138041243 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752887 | TCTCGGCTCACTGCA[A/G]CCTCCACCTCCCAGG | 7805 |
| rs138128274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742865 | ACTGTGAGGAGTAAA[C/T]GAGACTATCCCAGGA | 7805 |
| rs138163595 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | LAPTM5 | GRCh38.p7 | 1:30735240 | ATCAATCTGTAGCAC[C/T]GCCACACGCACTTGA | 7805 |
| rs138228753 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746522 | CTTCTCCCCAAGCTC[G/T]GAGAGCCCAGCTGGG | 7805 |
| rs138281498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750177 | TTTAGGAGCAGCCAG[C/T]GGGGGGCTCAGAGTT | 7805 |
| rs138351382 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759336 | CTTTGTCTAAGAGTA[A/G]CAAGACCAGAGGAAC | 7805 |
| rs138437828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740439 | ACGCCCCGCATACAA[C/T]TGGACCTTCCTCCAC | 7805 |
| rs138681301 | snp | A/G/T | 0.00279258 | 0.0372817 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742953 | TTAAAGAGGTGGGGT[A/G/T]GGGGGTAGAAGCTGA | 7805 |
| rs138781745 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738832 | ATCTTCCTCCCAAGC[C/T]CCAACTCCAGGGAAC | 7805 |
| rs138971241 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742201 | AGAGTGAGGCTATCA[C/T]CTTTACCAGCTGGTG | 7805 |
| rs139296332 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755864 | GGCCACCAGGGCCCA[C/T]AATCCTTCGTGGCAA | 7805 |
| rs139318803 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751747 | CAGTCTCAAAAAAAA[A/G]GGGCGGGGGGCCTTG | 7805 |
| rs139456282 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748695 | TGGGGCCACGCACTC[C/T]GCAGCAGCCCGGCCT | 7805 |
| rs139457821 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744710 | AGCAAGTTGAGGGAG[A/G]AGCCCAAGTCTCCCA | 7805 |
| rs139473840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753827 | ACACTAACGTTGAGA[C/T]GTTAGCAATAGAGGA | 7805 |
| rs139678458 | snp | C/T | 0.000552907 | 0.0166177 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739841 | CCAACTTGAGGTAGG[C/T]GGGCAGCTCAATGTA | 7805 |
| rs139680902 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741418 | TAGCCCACCATGCCC[C/G]GCCCCGTGGAGGCTC | 7805 |
| rs139827360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735392 | CAGCTGCTCCTGCTC[A/G]GACCTCTCATTCTGG | 7805 |
| rs139842545 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747582 | TAATGACAAACACAG[C/T]TTCCCCAAGCTGGCC | 7805 |
| rs139843639 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733861 | GGGTGGTGCTGGGCC[C/G]CCCTCTGGGGTCTTC | 7805 |
| rs139954312 | in-del | -/ACCA | 0.00630547 | 0.055794 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733530 | TTGCTTGACAAACTC[-/ACCA]ACTTTAGAATGGCCA | 7805 |
| rs140021791 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736325 | ATGCCCACCCACCAC[C/T]ACAGAAAGGCTGGGG | 7805 |
| rs140031902 | in-del | -/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737829 | CAGCCGTCACCTTGG[-/C]TCGACCGCCACAGCA | 7805 |
| rs140142281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744539 | AGACTTTCAAAGTCT[C/T]AAGATTCCAGGATTA | 7805 |
| rs140232148 | snp | A/C/T | 0.000182925 | 0.00956195 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737595 | GCCGCAGGGCAGGGA[A/C/T]CCACTCACCTTGAAG | 7805 |
| rs140239823 | snp | A/G | 0.000234667 | 0.0108295 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739836 | GGAGGCCAACTTGAG[A/G]TAGGCGGGCAGCTCA | 7805 |
| rs140301275 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750857 | TGACCAGGGAGGAAA[C/T]TGAGGCTGGGGGACG | 7805 |
| rs140306126 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741499 | ATGGTTCTCCAAAAG[G/T]TATGTGTGAAGATCT | 7805 |
| rs140666064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736927 | AGAAACAGCAGTCAG[A/G]TCCCCCTTGAGTCCT | 7805 |
| rs140826902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749041 | TGGACACCCAGCACG[G/T]AGCCTGGTGGCCATG | 7805 |
| rs140866028 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738187 | CGCCTCCCTTCTAAA[C/G]GTGGTGTTTATTTCC | 7805 |
| rs140866709 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732853 | AGAACAGATTCGCCT[A/G]TGACTGAATCGACTG | 7805 |
| rs141317083 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757311 | CCAAAGCACTTTCAC[A/T]TCTGCTGTTGGCTTT | 7805 |
| rs141331793 | snp | C/T | 0.000620725 | 0.0176062 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742440 | CCGCCACTCCACCGG[C/T]GTCCCCTGGACCTAC | 7805 |
| rs141401901 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746501 | TCCACCTGGACACAG[C/T]GCTGCCTTCTCCCCA | 7805 |
| rs141476532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745350 | ATCTTCCAGCCACCC[A/G]GGCTCTGCCTAAGGC | 7805 |
| rs141499795 | snp | C/T | 0.000656637 | 0.0181077 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739819 | CTCACAGCACGGCTC[C/T]GGGAGGCCAACTTGA | 7805 |
| rs141511104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750157 | GGTAGCTTATCAAAT[C/T]TCCCTTTAGGAGCAG | 7805 |
| rs141538379 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733322 | CATGTAAGCAAGCTA[G/T]TTGAAGAAATTGATT | 7805 |
| rs141561124 | in-del | -/TGTGTA | 0.478932 | 0.10045 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732368 | GAGTGTGTGGAGGGG[-/TGTGTA]TGTGGGTGTAGGGGG | 7805 |
| rs141803740 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745527 | GGCTCACCCTCCCCC[-/T]ATTTCACCTTTTCTC | 7805 |
| rs141877216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742919 | GAAGAGTGGTAACTG[C/T]TACTACTGAAGGTCA | 7805 |
| rs142053248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748535 | AAGGGAGTCAGATGT[A/G]TCACCATCAAGAGGA | 7805 |
| rs142227967 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750785 | TCTGTAAAATGGAGG[C/T]CCCCGTGGCAGCTGC | 7805 |
| rs142360434 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757457 | ACTCCTCACTCTTGC[A/G]GCATCTCCCCAGGGT | 7805 |
| rs142432128 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740769 | CCTGCACAAGGCAAA[C/T]GGCCTCCCCAGGCAG | 7805 |
| rs142512715 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759355 | GACCAGAGGAACTGG[A/C]GATCAGGAAACCAGG | 7805 |
| rs142725909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750398 | TGAACTTATACAGTC[A/G]GCCCTCTGTATCACG | 7805 |
| rs142775655 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749274 | AGAATTTCATTTCTA[C/T]GTAATTCTACAGATG | 7805 |
| rs142810679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739450 | TTTCTTCAACTTGGT[C/T]CCAAAGAAGAAATAA | 7805 |
| rs143033773 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746780 | ACCTCTCTGGGCCTC[A/G]GCTCCTCATCTGAGG | 7805 |
| rs143083490 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734953 | GCGCCTCCTGGAATC[A/G]ATATGAGACTAGCAA | 7805 |
| rs143164701 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742032 | CGGCCTGAGACAGGG[A/C]CAGGGTTGGTGAGGT | 7805 |
| rs143224849 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737303 | AGACCAACCACGCAG[C/G]TAGTGACAGTGGGGC | 7805 |
| rs143284664 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745682 | ACTCTGAGGGGCCCC[A/G]ACCTTCCACGAAGAT | 7805 |
| rs143367007 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732834 | TTGACCACAAGCCTC[A/G]GGCAGAACAGATTCG | 7805 |
| rs143402580 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753313 | CTCCCCATTCATCAA[A/G]CTTGAGTTGCTTGGA | 7805 |
| rs143459442 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738171 | CACACATTCTTTGAG[A/G]CGCCTCCCTTCTAAA | 7805 |
| rs143468732 | snp | A/C/G | 5.12872e-05 | 0.00506373 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30757737 | GACAGTGGACAAGCG[A/C/G]GGGTCCATGGTGCTG | 7805 |
| rs143486131 | snp | A/C/G | 0.000376118 | 0.0137093 | missense | LAPTM5 | GRCh38.p7 | 1:30757736 | GGACAGTGGACAAGC[A/C/G]GGGGTCCATGGTGCT | 7805 |
| rs143813905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740690 | GTCTTCAGGGACCAC[C/T]TGCTCCATTTCTCCA | 7805 |
| rs143831584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751996 | GCCCCCAAAGTGGAG[C/T]AGAGAAAAGAGCCCC | 7805 |
| rs144033203 | snp | G/T | 0.0217236 | 0.101931 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752371 | AAAGGACTCGGGCAG[G/T]TCCCACCCCTGGGGA | 7805 |
| rs144076860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734843 | GGTCCTTCCTCTGTG[C/T]TTATTGTCCCTGTGC | 7805 |
| rs144120035 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750567 | TTCTGATTTTGCAGG[A/T]AAAATTGAAATCAGC | 7805 |
| rs144121802 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741697 | CATGGTGATGAGCAG[A/G]AAGCTGGAGATCAGG | 7805 |
| rs144122342 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756276 | CATTGGCAGGAGCTC[A/G]GAAGGACAACCTCTG | 7805 |
| rs144212890 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740711 | CATTTCTCCATTTCT[C/T]TAGCTGAACCCTTTG | 7805 |
| rs144251668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750871 | ATTGAGGCTGGGGGA[C/T]GGGTGCCTTGTCCCA | 7805 |
| rs144278297 | snp | A/C/T | 0.00218374 | 0.0329716 | missense | LAPTM5 | GRCh38.p7 | 1:30757720 | CAGCAGCAGGTCTGG[A/C/T]GGACAGTGGACAAGC | 7805 |
| rs144448374 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741436 | CCCGTGGAGGCTCAT[A/G]TTACCAGGGAACTGA | 7805 |
| rs144620246 | snp | A/G | 6.60142e-05 | 0.0057448 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30737631 | GACAGTGATGAAGGC[A/G]ATGGAAAAGATGATC | 7805 |
| rs144621213 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755004 | GGAAAGCCCCCAGGC[C/T]CTGCCCTTTCTGGGA | 7805 |
| rs144680127 | in-del | -/TATT | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743293 | TTCCCCTAGCTGTTG[-/TATT]TGTTGAATGAATGAA | 7805 |
| rs144695098 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733214 | ATTAAATGGTTTGGA[A/G]GCTAACGTGATTTTT | 7805 |
| rs144849255 | snp | C/G | 5.27774e-05 | 0.00513672 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741701 | GTGATGAGCAGGAAG[C/G]TGGAGATCAGGTCAG | 7805 |
| rs144879372 | snp | A/G | 0.0219376 | 0.102409 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741621 | GGGGCAGGGGGCAGC[A/G]GGGCTCCTGAGCCCT | 7805 |
| rs145009467 | in-del | -/TGT | 0.0178098 | 0.0926698 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736159 | TGAGGCCTTCAGGGG[-/TGT]TGTTCTCACTGTACA | 7805 |
| rs145017797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751382 | TCTAACAGATTCTCA[C/T]CCAGGGTTTTCCCCA | 7805 |
| rs145073645 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750547 | CTAACATGAGTCCCA[C/T]ATTTTTCTGATTTTG | 7805 |
| rs145158983 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749778 | ATGAGCAGAGGCCAG[C/T]GTGCATGAGACGCAT | 7805 |
| rs145274770 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748730 | GCCTGCAGCTCCCCA[A/G]AGCCTGGCTTCTCTC | 7805 |
| rs145384305 | snp | C/T | 0.000688741 | 0.0185444 | missense | LAPTM5 | GRCh38.p7 | 1:30733899 | AAGACAGGGCTTCCT[C/T]GTAGGACGGCAGGAC | 7805 |
| rs145412760 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732036 | ACGCCTGATTAGGGA[A/G]ACATCAGGGTGCATC | 7805 |
| rs145547723 | snp | A/G | 0.000180099 | 0.00948773 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733641 | GACTCAGCCTAAAGC[A/G]TTGACCCAGTTGTGA | 7805 |
| rs145612606 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732022 | GGGGAGTGGAGTGCA[C/T]GCCTGATTAGGGAGA | 7805 |
| rs145636949 | snp | A/G | 0.000418806 | 0.0144647 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739840 | GCCAACTTGAGGTAG[A/G]CGGGCAGCTCAATGT | 7805 |
| rs145655716 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746502 | CCACCTGGACACAGC[A/G]CTGCCTTCTCCCCAA | 7805 |
| rs145717257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749251 | GCTCACAAAAGAACA[C/T]GCGCTGCAGAATTTC | 7805 |
| rs146112272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744152 | TACCAGGAGCACGGT[A/G]CATGCTCTAACTGCC | 7805 |
| rs146237962 | in-del | -/T | 0.0211228 | 0.100574 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741758 | GCTCAGGGGTGCCCC[-/T]GGGACCCCAGCCAGG | 7805 |
| rs146392377 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743603 | CCTATGACATACATA[C/G]AGTTCTCCAGGTAAC | 7805 |
| rs146490774 | snp | C/G/T | 6.82447e-05 | 0.00584109 | missense | LAPTM5 | GRCh38.p7 | 1:30757735 | CGGACAGTGGACAAG[C/G/T]GGGGGTCCATGGTGC | 7805 |
| rs146571415 | snp | C/G | 0.029116 | 0.117091 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756669 | CACAGCTCTGCCTGC[C/G]CTGCCTGTGACAGGA | 7805 |
| rs146589452 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751043 | GTCCTGGTTCCAGGC[C/T]GATGCTCTAGGCTCA | 7805 |
| rs146841958 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759369 | GAGATCAGGAAACCA[C/G]GGGCCAGGAGGGCCC | 7805 |
| rs146991472 | snp | C/G/T | 0.00518157 | 0.0506848 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742721 | CTTTACACACAGAGA[C/G/T]CCCATGTTCAGAATC | 7805 |
| rs147015491 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745509 | CACCTGCATTTAAAA[C/T]CCAGGCTCACCCTCC | 7805 |
| rs147094889 | snp | C/G | 6.95918e-05 | 0.0058984 | missense | LAPTM5 | GRCh38.p7 | 1:30757668 | ACTCACCACATGGTA[C/G]ATGGCCAGGGCGGTG | 7805 |
| rs147313891 | snp | A/G | 0.000511753 | 0.015988 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30757680 | GTAGATGGCCAGGGC[A/G]GTGGTTGCGATGCGG | 7805 |
| rs147380491 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750511 | TCGTGTCAACCTCGC[A/G]CCAGTCTTGAGAGAC | 7805 |
| rs147484958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735020 | GTGAGTGAATGAATC[G/T]TAGACTACCAGAACT | 7805 |
| rs147602366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745548 | ACCTTTTCTCAACAA[C/T]CCTGCGGCAGGGGAC | 7805 |
| rs147651932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748761 | TCCTCTTCACTCTTC[C/T]GCAGTTCTCGTCCTC | 7805 |
| rs147666160 | snp | A/G | 0.000173121 | 0.00930218 | missense | LAPTM5 | GRCh38.p7 | 1:30733907 | GCTTCCTCGTAGGAC[A/G]GCAGGACCACCTGGG | 7805 |
| rs147763685 | snp | A/C | 0.021333 | 0.101051 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748665 | AGCCCAGATACCACC[A/C]GACGCCCCCATTCCT | 7805 |
| rs147776668 | in-del | -/C | 0.0193772 | 0.0965046 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743779 | ACCCACCATCTGTTT[-/C]CCCCTTGCTGACTGT | 7805 |
| rs147844704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744764 | TCCCCTGACCCCCAA[A/T]ATGCCTCAGAGCCCT | 7805 |
| rs148056794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738173 | CACATTCTTTGAGAC[A/G]CCTCCCTTCTAAAGG | 7805 |
| rs148102865 | in-del | -/A | 0.0283406 | 0.115616 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746455 | CATTTCCAAGCCTCC[-/A]AGCCCTTGCCTTCCC | 7805 |
| rs148128857 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752206 | CACACACCTGTGTGC[C/T]AGCAGGGGGACCTGA | 7805 |
| rs148336435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745805 | TATTCAGCACCTACT[A/G]TGTGCTCAGACCTGC | 7805 |
| rs148522746 | in-del | -/C | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740400 | CAGCAGAGAGCCCCT[-/C]CCCCCCACCCCCCAC | 7805 |
| rs148532527 | snp | A/G/T | 0.000668606 | 0.0182717 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739884 | GGTGAGCAGGCACAG[A/G/T]AGATAGTCCATGATT | 7805 |
| rs148645642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748385 | CCCTCAGGGCTGCTC[C/T]ACCCTGACCCTGTGT | 7805 |
| rs148669049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734884 | GTTGTAATTGTATCT[A/G]TGTGTCTGAACTGTA | 7805 |
| rs148722734 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740740 | TGAGTTTCTGCACAA[G/T]CACCCACAGCCACCC | 7805 |
| rs149034623 | snp | G/T | 0.00693167 | 0.0584618 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741750 | AGGGAGGTGCTCAGG[G/T]GTGCCCCTGGGACCC | 7805 |
| rs149088114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745642 | CCACAGTCACAGAGC[A/G]AGGCAACCTCAGAGC | 7805 |
| rs149189353 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732688 | TGGGGCCAAACCTCC[C/T]CAGCTGCCACAACCG | 7805 |
| rs149360622 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743416 | GTTGGGGTGGCCCTA[G/T]AAACAACTGAAGTTC | 7805 |
| rs149415736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747782 | GTACCAGAGGGGATG[C/T]GGTGAAAACAGTGCA | 7805 |
| rs149503933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734645 | CACCTTACAGGTGAG[G/T]AAAGTAAGTTACCAG | 7805 |
| rs149678853 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744737 | CCCAGTGCTGTTCTG[A/T]TGCCTTCCCATTCCC | 7805 |
| rs149733442 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754005 | AATACATTTCCTCCT[C/T]GCCCAGTTTTGACGT | 7805 |
| rs149855768 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736372 | GTCAGCAGTGATGCT[C/G]TCTGTGTGGGGTGTG | 7805 |
| rs149909342 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741541 | GTGGGACCGCCTAAC[A/G]TACCCGCCTCCCACC | 7805 |
| rs150147226 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749179 | ATGGAAAAAATGAGT[G/T]AGCTACCCGCAACCA | 7805 |
| rs150173448 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738695 | CTGGGATCATGCAGG[G/T]CTGCTCCTACAGCCA | 7805 |
| rs150479832 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758920 | CAGAGCAGACAGGAA[C/T]TGCCATGAAGCCCTG | 7805 |
| rs150641652 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742936 | ACTACTGAAGGTCAG[G/T]CTTAAAGAGGTGGGG | 7805 |
| rs150866853 | snp | C/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751751 | CTCAAAAAAAAGGGG[C/G]GGGGGGCCTTGTGTT | 7805 |
| rs150887812 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750160 | AGCTTATCAAATCTC[C/T]CTTTAGGAGCAGCCA | 7805 |
| rs150907207 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741348 | CTGCTTCCACCTGCC[A/G]TTTAAAAGGATGTGA | 7805 |
| rs150944541 | in-del | -/TGAA | 0.0314385 | 0.121371 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743300 | AGCTGTTGTATTTGT[-/TGAA]TGAATGAATGAATGA | 7805 |
| rs150960790 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744627 | GAGCCTGCATGTACT[C/T]GTTTTATAAGCTTCC | 7805 |
| rs151116074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736057 | ATAAAAAACAGAAGG[C/G]GAGCTGGGGGACGGA | 7805 |
| rs151241209 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757891 | CGTCACAGCTGGGGC[A/G]GGGCAGCTGGGGAGG | 7805 |
| rs180697235 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750464 | CGATGTGGAACCTGC[A/G]GATAGGGAGGGCCGA | 7805 |
| rs180706459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743128 | CCTCAGGGAACAATA[A/G]CATCTTCCTCATAGG | 7805 |
| rs180914116 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747889 | GGCGTGGTGATGACA[A/G]TGATGATCAGAGATG | 7805 |
| rs180959081 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737206 | AATCTCAGGTACATT[C/T]TGATGCCTGAATTAC | 7805 |
| rs181359131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746897 | CACCATAAACAAGCA[C/G]AATTGGGTGGTGGTT | 7805 |
| rs181366382 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738668 | GTTGCAATTCACATG[C/T]CAAAGCCCTCTCTGG | 7805 |
| rs181459031 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737425 | TAAATGGGCTGTCTC[A/G]GAGGATCCCAAGTAA | 7805 |
| rs181468729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754525 | TGGGTGACAGAGCAA[A/G]ACCCCATCTCTTAAA | 7805 |
| rs181520936 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754895 | GTCCAGATGACAGCC[A/G]GCATGGGCTATTGAC | 7805 |
| rs181668383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751471 | GGGCCAGGCACTATG[A/G]CCCACGCCTATAATC | 7805 |
| rs181689840 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748092 | AGGCCCAGGACCCAC[A/C]GTCTCAGAAGCAGGC | 7805 |
| rs182044510 | snp | A/G/T | 0.000136812 | 0.00826977 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742457 | TCCCCTGGACCTACC[A/G/T]ATCCTGAGGTAGCCC | 7805 |
| rs182279028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756152 | TACCTGTGAGGCGCC[C/T]CTGCATGCCACACTG | 7805 |
| rs182282731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745271 | GGGCCTTGCCCAAGG[C/T]CTCCCAGCTGGTCAT | 7805 |
| rs182493052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750528 | CAGTCTTGAGAGACA[A/G]GTTCTAACATGAGTC | 7805 |
| rs182543066 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753028 | CTCAAGTGATCCACC[C/T]GCCTCAACCTCCCAA | 7805 |
| rs182799056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748707 | CTCCGCAGCAGCCCG[A/G]CCTGGCTGCCTGCAG | 7805 |
| rs182800279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734113 | GTAGTGGACATATTT[A/G]CCTTTGCCTATTCAG | 7805 |
| rs182863212 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749185 | AAAATGAGTTAGCTA[A/C]CCGCAACCACACAGA | 7805 |
| rs182863518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740573 | CATTCATATGCTCTC[A/G]CAGCTGGGGACAAAA | 7805 |
| rs182869382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756412 | TGTGCGTCAGGCGTG[A/G]TTCTGCATGCTTTGT | 7805 |
| rs182908551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753792 | ACGAATATTCATTCA[C/T]CCATTGCAACAAACG | 7805 |
| rs183127676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757519 | AGGCCCAGAGCAGGA[A/C]AGGGATTTGCCCAGG | 7805 |
| rs183149729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741077 | TTTGCCTCGGGCCCA[A/G]GAGCCCCTCGTTGTC | 7805 |
| rs183394200 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743433 | AACAACTGAAGTTCA[A/G]CCACAAAACTGCAGT | 7805 |
| rs183406883 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734945 | TTTTCTCTGCGCCTC[C/T]TGGAATCGATATGAG | 7805 |
| rs183563900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747337 | GAGGATGTTACCAGC[A/G]GGGAAATATGGCCCA | 7805 |
| rs183822203 | snp | C/T | 0.000140002 | 0.00836549 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741648 | CCCTCACCTTGACTA[C/T]GCCGATCAGTAGGCT | 7805 |
| rs183831808 | snp | A/C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758523 | CGAAGAGGCGTGCAG[A/C/G]GCTCCAGACAAGGAC | 7805 |
| rs183864660 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750071 | GTGCTGTGACTGGGC[A/G/T]CTAGCAGCTAACTTT | 7805 |
| rs184190711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753461 | GTTGGCAGAACCTTT[C/T]CTTAGTACGATGTTC | 7805 |
| rs184218857 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754100 | CTGACAGTGGAATTC[C/T]GGGCACTCTGGGGAA | 7805 |
| rs184456118 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758890 | GAGCCCCTTTGCAAT[A/G]CCAAGCTTCTAGTGC | 7805 |
| rs184471433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736607 | TCCAACTTTTTTTTT[C/T]TTATGTTTTGTAGAG | 7805 |
| rs184637244 | snp | A/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750503 | ACACTCTCTCGTGTC[A/T]ACCTCGCGCCAGTCT | 7805 |
| rs184789858 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737331 | GGCTTGGATTCAAAC[G/T]CAGGCCAGTCCAAAT | 7805 |
| rs184793491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754284 | TGCCTGTAATCCCAG[C/T]GCGTTGGGAGGCCAA | 7805 |
| rs185166398 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749480 | TTCTATAGGTAAATT[A/G]TACATCAAGAAAAGG | 7805 |
| rs185196442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742307 | TGCGGATGAAACAGC[C/T]GAGGCCCCAAGAAAG | 7805 |
| rs185240367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743191 | AAAGTACCTGGCAGA[C/T]AGTAAGCACTCAATC | 7805 |
| rs185326524 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746703 | TGAAGATAAGAGCTC[A/G]GGTGCTGGGGTCAGA | 7805 |
| rs185507927 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732640 | CTCCCTGGAGGACCC[C/T]GACACACAGGGAAGC | 7805 |
| rs185522668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752402 | CCTCTCCACCCTCCT[C/T]CCCGACACACCTCGT | 7805 |
| rs185898706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755193 | ATTGGTTCTCAACTG[A/G]GAGAGATTGGGCCCC | 7805 |
| rs186017150 | snp | A/C | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732110 | CACCCCTCGCTCAGC[A/C]TGGCCCATGGGAGGA | 7805 |
| rs186018333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739215 | GAGACATGAACACAC[A/G]GATGTTCATACCAAG | 7805 |
| rs186026816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751084 | CTCACTTCCTGGAGG[C/T]CTCGGGGCCAGGTTG | 7805 |
| rs186075177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739991 | TGCAGCCAACACTCC[G/T]CCACCCAGCCTGATA | 7805 |
| rs186087067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756273 | TTGCATTGGCAGGAG[C/G]TCGGAAGGACAACCT | 7805 |
| rs186241402 | snp | C/T | 0.00294455 | 0.0382586 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742599 | TGCATCACGGCCCCC[C/T]GACCAGCCCCTCCCA | 7805 |
| rs186250146 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737767 | CAGCACCCACACATC[C/T]GGGAATAATGATCCC | 7805 |
| rs186257577 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754619 | AAGAATAGATTTTTT[A/T]AAAAAAGAAAGAAAG | 7805 |
| rs186897776 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745424 | CCCATCCCCTCTCCC[C/T]CTGCAGTCCCCCCTC | 7805 |
| rs186914523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743619 | AGTTCTCCAGGTAAC[C/T]TCTGCCCATATAAAG | 7805 |
| rs186963133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753908 | CGTAAATCTAAAACC[C/G]TTCTAAGTACGTGCT | 7805 |
| rs186983406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747905 | TGATGATCAGAGATG[C/T]TGTTGGTGATGTTGG | 7805 |
| rs187152461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748445 | TTATTATTATGGCCC[C/T]TCCCTGAAGCTCAGT | 7805 |
| rs187231994 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748920 | ACATTTCCTCATCTG[C/T]AGAAGGGAGAGAAGA | 7805 |
| rs187468057 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757155 | CACTGGAGGCACAAA[G/T]GGGAGATCCCCACTT | 7805 |
| rs187478515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749745 | AATGGAAAAAGTGTT[C/G]CAGGCAGAGGAAAGG | 7805 |
| rs187766085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734719 | CTCATCCTCTCTTCC[C/T]GGAAAGCCTCCTTCT | 7805 |
| rs187814056 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744881 | TTTCTTTCTAAATTA[C/G]ACGCATGTGTTGCTG | 7805 |
| rs187822247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734979 | AGCAAAGAGTGAGAG[G/T]CAGTAAATACTGAAT | 7805 |
| rs187828604 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753739 | GTAAGAGGAAAGCTG[A/G]GGAAATAGGGGTGAA | 7805 |
| rs188056508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753152 | ACCATTGGATTATAA[C/T]CCAAAGCATACAGTA | 7805 |
| rs188066738 | snp | C/T | 0.00172419 | 0.0293108 | missense | LAPTM5 | GRCh38.p7 | 1:30757693 | GCGGTGGTTGCGATG[C/T]GGACATTGAAGCAGC | 7805 |
| rs188111001 | snp | C/G | 1.64953e-05 | 0.00287182 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735288 | AAGGCCCAGGTCAGG[C/G]TGTGCTTTGCTGAGC | 7805 |
| rs188300737 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747353 | GGGAAATATGGCCCA[C/G]AGAGAGACAGCGACC | 7805 |
| rs188338778 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741170 | GGGGCCTTCCAGGGC[A/G]TAGGTCCCCCTCAGG | 7805 |
| rs188512510 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746835 | TCACAGGATTGCTGA[A/G]GTCAAATGGAATCGT | 7805 |
| rs188547516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750413 | GGCCCTCTGTATCAC[A/G]GGCTCTGCATCTGAG | 7805 |
| rs188620443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749221 | CTCCCAAACATAACG[C/T]TGGGAGAAAGAAGTG | 7805 |
| rs189144870 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746084 | CAGCCACTCAGAGCT[C/T]AGGAGACAAGAGCTG | 7805 |
| rs189292557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736778 | GACCTATGTTACTTT[C/T]ATAATCAGAAAAGAA | 7805 |
| rs189421037 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742220 | TACCAGCTGGTGGGG[A/G]TTTGCAAAGTGCCAT | 7805 |
| rs189430683 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758591 | CCAGGCCCTGGGCTA[A/G]GCTTCTCTTCTAGGT | 7805 |
| rs189480573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754286 | CCTGTAATCCCAGCG[C/T]GTTGGGAGGCCAAGG | 7805 |
| rs189563058 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754631 | TTTAAAAAAAGAAAG[A/G]AAGTTTGCTGGGTTC | 7805 |
| rs189590269 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754260 | CTCTAGACTGGGCTC[A/G]GTGGCTCATGCCTGT | 7805 |
| rs189738640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749164 | GGAGTATACACAGCA[A/G]TGGAAAAAATGAGTT | 7805 |
| rs189831594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737806 | CACACACACGAGCAC[A/G]GCGTGGCACAGCCGT | 7805 |
| rs189861928 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742700 | CATCTCAGACAAAAG[A/C]GTGGCCTTTACACAC | 7805 |
| rs190122839 | snp | A/C/G | 0.00378957 | 0.0433671 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742427 | TGTCCTCCTCCCCCC[A/C/G]CCACTCCACCGGCGT | 7805 |
| rs190155852 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748705 | CACTCCGCAGCAGCC[C/T]GGCCTGGCTGCCTGC | 7805 |
| rs190282439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752865 | AGGCTAGAGCGCAGT[A/G]GCGCGATCTCGGCTC | 7805 |
| rs190363581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750509 | TCTCGTGTCAACCTC[A/G]CGCCAGTCTTGAGAG | 7805 |
| rs190381093 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759212 | TAAGCCTTGCTGAGG[C/T]CTGACATCATAGAAA | 7805 |
| rs190501569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751319 | GCAGTGGCAGAGAAC[A/G]TGGCCTCTCTGTCCA | 7805 |
| rs190649723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739227 | CACAGATGTTCATAC[C/T]AAGAGCTGGTGGCAG | 7805 |
| rs190886232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743200 | GGCAGATAGTAAGCA[C/T]TCAATCTGTGCTGTT | 7805 |
| rs190909258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756142 | AGGGACTTGCTACCT[A/G]TGAGGCGCCCCTGCA | 7805 |
| rs190929639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740124 | ACCCAGGCCCTGAAT[A/G]AGAGGAGTCTTGGTG | 7805 |
| rs191036028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756280 | GGCAGGAGCTCGGAA[A/G]GACAACCTCTGAGTT | 7805 |
| rs191218545 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732831 | TGCTTGACCACAAGC[C/G]TCGGGCAGAACAGAT | 7805 |
| rs191227716 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741544 | GGACCGCCTAACATA[C/T]CCGCCTCCCACCCTC | 7805 |
| rs191458225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743671 | CCTCTAGTCGGTGCC[C/T]TATCTCTATTAATAT | 7805 |
| rs191628270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750020 | CTCGGACGGCTCAGA[C/T]GGCGCTGGAGGAGGT | 7805 |
| rs191901576 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753386 | AGAAAAAAAGAGTAA[C/G]TTTACAAAGGAGTAA | 7805 |
| rs191904231 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745155 | ATTTGTACAGCCTAA[C/T]TCCATGCCACATGAT | 7805 |
| rs191970330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735034 | CTTAGACTACCAGAA[C/T]TGAAAGAGAACACAT | 7805 |
| rs191983568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753772 | ACTGACTTTAATAAC[A/T]GCCCACGAATATTCA | 7805 |
| rs192193976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734923 | TAAGGCAGAGGTGGC[A/G]TCTTAGTTTTCTCTG | 7805 |
| rs192319085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748020 | GAACCCCCGATTCTG[A/G]GGTTCAAAGACCAGT | 7805 |
| rs192378261 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754274 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCGCGTT | 7805 |
| rs192470303 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745616 | AGACTCATAGAGGGC[A/G]GGGGACCAGCCCACA | 7805 |
| rs192525086 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758323 | ACTATTATGATCCCC[A/G]TTTTACAGATGAAGA | 7805 |
| rs192653777 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757178 | CCCCACTTCTCATCC[A/C]CTCGAGTGGCCCAGG | 7805 |
| rs192682842 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742294 | GAACATCCCCATTTG[C/T]GGATGAAACAGCTGA | 7805 |
| rs192695635 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758839 | TAGGAAGTACATGCA[A/G]CATTTCTGGAAGAAG | 7805 |
| rs192791284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735639 | GACATGTTTTCTTCA[A/G]AATTGCTTCCGATAT | 7805 |
| rs192810629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746223 | TTTCCCCTGGGGCCA[C/T]TGGGATGACAGAACG | 7805 |
| rs192875266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741006 | GGGACCCAGGGACCG[C/T]GGGTTCCTCTTCTGC | 7805 |
| rs193001972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754080 | TTAACCCAGACAATG[C/T]ATTTCTGACAGTGGA | 7805 |
| rs193294653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749345 | GGGCGGGGCAGTGGC[A/G]AGGCGGGGGCTCTAG | 7805 |
| rs199569455 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740334 | GAGTGAACAGGAGGG[-/A]GGGGCGGGGCACTGG | 7805 |
| rs199707557 | snp | C/G | 1.77212e-05 | 0.00297663 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733924 | CAGGACCACCTGGGA[C/G]AGACAGAGAGATGAG | 7805 |
| rs199717377 | snp | A/G/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732330 | GGTGTTTGGGTGTAT[A/G/T]TGTGGGTGTGTGGGG | 7805 |
| rs199814092 | in-del | -/GAAGGGA | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733036 | AACAATTGTGTGTTT[-/GAAGGGA]CTGTTTTATGATGAA | 7805 |
| rs199840399 | in-del | -/AT | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732211 | GTGTGGGGGGTGTGA[-/AT]GTGTGTGGGTATATG | 7805 |
| rs199971598 | snp | A/G | 0.00379584 | 0.0433994 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741724 | CAGGTCAGCTGAAAG[A/G]CAAGGAGAGCAGGGA | 7805 |
| rs200376170 | snp | A/C | 0.00199792 | 0.0315431 | missense | LAPTM5 | GRCh38.p7 | 1:30737674 | AACTGGTTATGAGGC[A/C]TATCCTCCTGGCTGG | 7805 |
| rs200387678 | in-del | -/GTT | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732178 | CATGGGTGTGTGGGG[-/GTT]GTGGGCGTGTGTGGA | 7805 |
| rs200738089 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740304 | CACCAGGGCTAGATC[A/G]GGGAAGGAGACTAGG | 7805 |
| rs200757747 | snp | G/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732351 | GTGTGTGGGGGTGGG[G/T]GTGAGTGTGTGGAGG | 7805 |
| rs200768092 | in-del | -/TAT | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732382 | GTGTGGGTGTAGGGG[-/TAT]GTGTGGGTGAGTCCT | 7805 |
| rs200810512 | snp | A/G | 0.000100545 | 0.00708958 | missense, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739037 | TCCAGCAGCTGCAGC[A/G]TCATCAGGGGGAACT | 7805 |
| rs200884933 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734948 | CTCTGCGCCTCCTGG[-/A]AATCGATATGAGACT | 7805 |
| rs200965667 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747948 | GGGTGACGGCAATGG[A/G]GACATCAGGATAGGA | 7805 |
| rs201163248 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753098 | TACTTTTTTTTTTTT[A/G]CAATTTAAAAGTAGT | 7805 |
| rs201201887 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30737688 | CATATCCTCCTGGCT[A/G]GGGAGGTAATTCTGC | 7805 |
| rs201239677 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741711 | GGAAGCTGGAGATCA[A/G]GTCAGCTGAAAGGCA | 7805 |
| rs201359245 | in-del | -/AGTGTGGGTGT | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732309 | TGGGTATGTGGGGGG[-/AGTGTGGGTGT]TTGGGTGTATTTGTG | 7805 |
| rs201414211 | snp | C/G | | | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739066 | CTTGGAGGAGCTCTG[C/G]GGAGGACAAATACAA | 7805 |
| rs201454088 | in-del | -/CAC | | | cds-indel | LAPTM5 | GRCh38.p7 | 1:30733529 | GTTGCTTGACAAACT[-/CAC]CAACTTTAGAATGGC | 7805 |
| rs201599215 | in-del | -/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741754 | AGGTGCTCAGGGGTG[-/C]CCCTGGGACCCCAGC | 7805 |
| rs201742748 | in-del | -/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732174 | GTTTACATGGGTGTG[-/T]GGGGGTGGGCGTGTG | 7805 |
| rs201831542 | in-del | -/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736598 | GCCACCACATCCAAC[-/T]TTTTTTTTTTTATGT | 7805 |
| rs201863165 | snp | C/G | 0.00536235 | 0.0515016 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742582 | CATCAGTCAGCTGAG[C/G]CTGCATCACGGCCCC | 7805 |
| rs201964781 | snp | G/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733139 | TGAATTAACAATTAT[G/T]CAGCCACTCAGAGGT | 7805 |
| rs367632339 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735166 | ACCCACCTGCAGCCA[C/T]ACTCACCTTCTGGAG | 7805 |
| rs367648972 | snp | A/G | 6.45182e-05 | 0.00567934 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739085 | GGACAAATACAAGGA[A/G]GAGGAATGAGGAGCA | 7805 |
| rs367849875 | snp | A/G | 1.76752e-05 | 0.00297276 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739949 | GGTTCTGAAAGGTAG[A/G]CCCAGCACCGTCAAG | 7805 |
| rs367875278 | snp | A/G | 4.88556e-05 | 0.00494221 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742592 | CTGAGCCTGCATCAC[A/G]GCCCCCCGACCAGCC | 7805 |
| rs367878097 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754618 | AAGAATAGATTTTTT[-/A]AAAAAAAGAAAGAAA | 7805 |
| rs367888798 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758780 | TGGAATCTCTACTCC[C/T]TCCTCAGATGATAAA | 7805 |
| rs367914977 | snp | C/T | 5.66802e-05 | 0.00532324 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733819 | ACTGGGGCTGGGGCC[C/T]GGCGAGGGTCACACC | 7805 |
| rs368099878 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30735236 | CTTGATCAATCTGTA[A/G]CACCGCCACACGCAC | 7805 |
| rs368122353 | snp | C/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740534 | TTCTTCAATTGAAAG[C/G]AAGTGACCACCATGA | 7805 |
| rs368140512 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757092 | TGGTGGGCAGAAGGC[C/T]GTGGTTTGACTGAGC | 7805 |
| rs368151353 | snp | C/T | 1.86659e-05 | 0.00305493 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733822 | GGGGCTGGGGCCTGG[C/T]GAGGGTCACACCTCT | 7805 |
| rs368162817 | snp | C/T | 0.000261682 | 0.0114356 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742493 | GGAGAGCTTGCAGGA[C/T]GCCTTGCCATGGGCC | 7805 |
| rs368273555 | snp | A/G/T | 0.000227017 | 0.0106521 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741652 | CACCTTGACTACGCC[A/G/T]ATCAGTAGGCTCAGG | 7805 |
| rs368441175 | snp | C/T | 0.000115612 | 0.00760214 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735314 | TGAGCGTCCTTCTCA[C/T]GCTCCAGCAGGCCTA | 7805 |
| rs368516455 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739276 | GGTCTCCAGACTCCC[A/G]GGCCAGGGCCCTTCC | 7805 |
| rs368573187 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746967 | TCTCTGAGCACCTAC[C/T]GCCTCCAAACTCTGT | 7805 |
| rs368580907 | in-del | -/CAAC | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733532 | GCTTGACAAACTCAC[-/CAAC]TTTAGAATGGCCAAT | 7805 |
| rs368592373 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748115 | AAGCAGGCAGGCGGA[C/G]ACCCACCATCTGAGA | 7805 |
| rs368595498 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742350 | CAGAGGTCATCCATC[A/G]TCCATGGAGAGGTGG | 7805 |
| rs368658904 | snp | A/G | 0.000107848 | 0.00734249 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733934 | TGGGAGAGACAGAGA[A/G]ATGAGGGCTGAGTAT | 7805 |
| rs368955879 | snp | A/G | 4.13787e-05 | 0.00454837 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742579 | AAGCATCAGTCAGCT[A/G]AGCCTGCATCACGGC | 7805 |
| rs369299830 | snp | C/T | 0.000153988 | 0.00877328 | missense | LAPTM5 | GRCh38.p7 | 1:30737681 | TATGAGGCATATCCT[C/T]CTGGCTGGGGAGGTA | 7805 |
| rs369379575 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741224 | GATAGAGCTGCATGC[A/G]TCCTACTTTCCCCCT | 7805 |
| rs369470045 | snp | C/T | 1.69585e-05 | 0.00291187 | missense | LAPTM5 | GRCh38.p7 | 1:30757688 | CCAGGGCGGTGGTTG[C/T]GATGCGGACATTGAA | 7805 |
| rs369537054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740902 | CTCCGGCCCTGCAAG[A/G]GCCAGGCCCCTGTCT | 7805 |
| rs369548241 | snp | A/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759697 | GTCTCATTTTAAAAG[A/C]AATGCATTTAAATAA | 7805 |
| rs369608835 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740060 | CCTGCCCTCCTCAGT[G/T]GAGGTCACCTCCCTC | 7805 |
| rs369709523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749196 | GCTACCCGCAACCAC[A/G]CAGACGAAGCTCCCA | 7805 |
| rs369821802 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757227 | GGAAGAATCGGGGCT[A/G]TGTCTGCGGCCGACC | 7805 |
| rs370009551 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741249 | CCCCCTTCTTCGGCT[A/C]CTCTCATCCATTACA | 7805 |
| rs370223312 | snp | G/T | 3.65871e-05 | 0.00427694 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757787 | ACTGAAGGGGAAAGA[G/T]CCTGGTGCCTGGAGC | 7805 |
| rs370229354 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733299 | CTCATGGTTGGCTAA[C/T]TGATTATCATGTAAG | 7805 |
| rs370272502 | snp | A/C | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739019 | AGGATGCTCAGGCAG[A/C]AGTCCAGCAGCTGCA | 7805 |
| rs370275111 | snp | C/T | 4.94295e-05 | 0.00497115 | missense | LAPTM5 | GRCh38.p7 | 1:30735208 | TTCTCTTCTCCTCCA[C/T]CGAGTTCATGCACTT | 7805 |
| rs370375145 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739971 | ACCGTCAAGTGTCCC[C/T]TGCATGCAGCCAACA | 7805 |
| rs370701266 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754865 | ATGATGTGCAGAGTC[A/G]TCACCCATGGCTGGG | 7805 |
| rs370775118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736261 | TGGCATTAGGTGACA[A/G]CAGAGACTGCCCAGG | 7805 |
| rs370870412 | snp | A/G | 2.27384e-05 | 0.00337175 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733783 | AAAAGCAGATTATGA[A/G]GCAGCTCCACCCCTC | 7805 |
| rs370874664 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751328 | GAGAACGTGGCCTCT[C/T]TGTCCAGCCCAGGGG | 7805 |
| rs370942564 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746600 | CTCCCCCAACAATGC[A/G]CAGGCAGACAGCATG | 7805 |
| rs370947046 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741391 | TTCTCACCAAAGTGT[C/G]GGTGACCAGCATAGC | 7805 |
| rs371021746 | snp | A/T | 0.000153988 | 0.00877328 | missense | LAPTM5 | GRCh38.p7 | 1:30733842 | GTCACACCTCTGAGT[A/T]TGGGGGTGGTGCTGG | 7805 |
| rs371054508 | snp | A/T | 6.75687e-05 | 0.00581204 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737720 | ACAGATTTGGGGGCC[A/T]CATCAATGTCTCTGG | 7805 |
| rs371173092 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742275 | ATGTGGGTGGGGTCA[A/G]GTGGAACATCCCCAT | 7805 |
| rs371204720 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740104 | GGGGACAGGGAGTGG[A/G]TAAGACCCAGGCCCT | 7805 |
| rs371387674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746066 | GCAACCAAGCCCCAG[C/T]CCCAGCCACTCAGAG | 7805 |
| rs371510323 | snp | A/G | 0.00015287 | 0.00874138 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739097 | GGAGGAGGAATGAGG[A/G]GCAGCAATTAAAGTC | 7805 |
| rs371534577 | snp | A/C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746752 | GAGCTCTGCACCCTT[A/C/G]AGCCAGCCACTAACC | 7805 |
| rs371584502 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748148 | TTCAGGGAGGTAAAG[A/G]TTATAGAGAAAGGAC | 7805 |
| rs371661575 | snp | A/C | 1.76207e-05 | 0.00296817 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742535 | GTGCTCGATGAACAA[A/C]AAGACGCTCATGATC | 7805 |
| rs371742269 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757061 | CTAATGATTAGCACA[A/G]GTCTCAAGTTCTCTT | 7805 |
| rs371763856 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750178 | TTAGGAGCAGCCAGT[C/G]GGGGGCTCAGAGTTG | 7805 |
| rs371790554 | snp | C/T | 3.29565e-05 | 0.00405921 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30735251 | GCACCGCCACACGCA[C/T]TTGAACATGTAGACC | 7805 |
| rs371912748 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736644 | TCTTGCTATGTTGCC[C/T]AGGTTGGTTTTGAAC | 7805 |
| rs372136396 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751574 | TGAAACCCCATCTCT[C/T]CTAACGATACAAAAC | 7805 |
| rs372418272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748865 | GTGCAGCCGCTGATC[C/T]CCTGTGGGATCCTGG | 7805 |
| rs372441500 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741585 | GCACTGCCCACCACC[A/T]GTGGGTGTGAATAAC | 7805 |
| rs372468309 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740483 | GGGTCCAAAGTCACA[A/G]TAAGAGGCCCTGCCA | 7805 |
| rs372513002 | snp | A/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754153 | TTCTGGGCAAAAGTG[A/T]CTTCTGGGGGTGTCC | 7805 |
| rs372634338 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744218 | TGTCTCATCAGGAAA[G/T]TTGAGAACACCCCAA | 7805 |
| rs372636176 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749937 | GGGTGGGGCCTCTGG[A/G]GTTAGAGAGAAAGGG | 7805 |
| rs372643259 | in-del | -/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748635 | GCACTATCTCCCCAA[-/C]CCACCTCTCCAGCCA | 7805 |
| rs372654193 | snp | A/G | 1.65064e-05 | 0.00287279 | missense | LAPTM5 | GRCh38.p7 | 1:30737671 | ATGAACTGGTTATGA[A/G]GCATATCCTCCTGGC | 7805 |
| rs372996082 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757999 | GGACAGACCCTAACA[C/T]GGTCATCATGCCCTT | 7805 |
| rs373172801 | snp | A/G/T | 0.000186024 | 0.0096426 | missense | LAPTM5 | GRCh38.p7 | 1:30757694 | CGGTGGTTGCGATGC[A/G/T]GACATTGAAGCAGCA | 7805 |
| rs373209927 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750189 | CAGTGGGGGGCTCAG[A/C]GTTGGCCTCCAGGTA | 7805 |
| rs373279157 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748678 | CCAGACGCCCCCATT[C/T]CTGGGGCCACGCACT | 7805 |
| rs373280418 | snp | C/G | 0.000416902 | 0.0144318 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741607 | GTGAATAACAGGAAG[C/G]GGCAGGGGGCAGCGG | 7805 |
| rs373435764 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736965 | CCATGCTGAATAAAC[A/G]CTCAGGTCTTTGTTG | 7805 |
| rs373596960 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736223 | GAGAAGATGCTAAAA[C/G]GGGCAAGGTTCTGTT | 7805 |
| rs373642370 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736917 | TCAGGTATTAAGAAA[C/T]AGCAGTCAGGTCCCC | 7805 |
| rs373787269 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756981 | GAGTCACCAGGAAAG[A/G]AGGAACCAGTGACAG | 7805 |
| rs373851627 | snp | A/C/G | 0.000130513 | 0.00807728 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741633 | AGCGGGGCTCCTGAG[A/C/G]CCTCACCTTGACTAC | 7805 |
| rs373920363 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746572 | GCCATCCCATGACAG[A/G]TACAAGGCTTCTCTC | 7805 |
| rs373930174 | snp | C/T | 3.66703e-05 | 0.0042818 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757788 | CTGAAGGGGAAAGAG[C/T]CTGGTGCCTGGAGCA | 7805 |
| rs373967290 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737717 | GCAACAGATTTGGGG[A/G]CCACATCAATGTCTC | 7805 |
| rs374051098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750272 | CCACTCCCCAAACGA[C/T]TCCCTAAAACCATCA | 7805 |
| rs374086132 | snp | A/G | 0.000322558 | 0.0126955 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739959 | GGTAGGCCCAGCACC[A/G]TCAAGTGTCCCCTGC | 7805 |
| rs374167496 | snp | A/G | 0.000153988 | 0.00877328 | missense | LAPTM5 | GRCh38.p7 | 1:30733853 | GAGTATGGGGGTGGT[A/G]CTGGGCCCCCCTCTG | 7805 |
| rs374196809 | snp | C/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750584 | AAATTGAAATCAGCT[C/G]TTTACACATGGGCTC | 7805 |
| rs374364535 | snp | C/T | 1.69565e-05 | 0.00291169 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737727 | TGGGGGCCACATCAA[C/T]GTCTCTGGACATAAG | 7805 |
| rs374367156 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758662 | TCACTTTCAGGGCCT[C/T]AAGACCCAATCCCCA | 7805 |
| rs374516423 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746677 | CCCTTCATTCTATGC[C/T]GGTGAGATCATGAAG | 7805 |
| rs374608139 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | LAPTM5 | GRCh38.p7 | 1:30735216 | TCCTCCACCGAGTTC[A/G]TGCACTTGATCAATC | 7805 |
| rs374624929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743687 | TATCTCTATTAATAT[A/G]GCCCTAAGTTTACAT | 7805 |
| rs374746117 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759398 | CCTGAGGCCATGCTG[A/G]GGAGTCTGCATTTGA | 7805 |
| rs374760602 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737458 | TCAGAGGAGCTGGCA[C/T]GGGAAAGCAAGAGAA | 7805 |
| rs374774651 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746736 | GCCCCAGGCCCCAGC[C/T]GAGCTCTGCACCCTT | 7805 |
| rs374941421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749743 | GCAATGGAAAAAGTG[A/T]TCCAGGCAGAGGAAA | 7805 |
| rs374955908 | snp | A/C/T | 7.83392e-05 | 0.00625807 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738908 | AGGCCACACAGCCAG[A/C/T]AAATGGGCATGGTTC | 7805 |
| rs375164990 | snp | C/G/T | 0.000247521 | 0.0111221 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735303 | CTGTGCTTTGCTGAG[C/G/T]GTCCTTCTCACGCTC | 7805 |
| rs375249125 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750712 | CAGACACCTGGGCTC[A/G]GGTTCTTTATCTAAC | 7805 |
| rs375292625 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745816 | TACTGTGTGCTCAGA[C/T]CTGCACGCACAGGCT | 7805 |
| rs375749949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743650 | AACAAGAAAACTGTC[C/G]CCTCCCCTCTAGTCG | 7805 |
| rs375844937 | snp | C/T | 4.36091e-05 | 0.00466933 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757611 | CACCGCAGACATTCA[C/T]ACTCACACAAGCACG | 7805 |
| rs375929465 | snp | A/G | 0.000567508 | 0.0168354 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737586 | CCTCCCAGAGCCGCA[A/G]GGCAGGGATCCACTC | 7805 |
| rs375995678 | snp | G/T | 1.65083e-05 | 0.00287296 | missense | LAPTM5 | GRCh38.p7 | 1:30737672 | TGAACTGGTTATGAG[G/T]CATATCCTCCTGGCT | 7805 |
| rs376132681 | in-del | -/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737449 | AAGTAAAGTCAGAGG[-/G]AGCTGGCATGGGAAA | 7805 |
| rs376231516 | snp | G/T | 1.70653e-05 | 0.00292102 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739791 | CTGTCCGGTGAGAGG[G/T]GGGGGCTGGGTACTC | 7805 |
| rs376284297 | snp | A/G | 0.000115448 | 0.00759675 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735162 | TGGCACCCACCTGCA[A/G]CCACACTCACCTTCT | 7805 |
| rs376441273 | snp | A/G | 6.07773e-05 | 0.00551226 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741603 | GGGTGTGAATAACAG[A/G]AAGGGGCAGGGGGCA | 7805 |
| rs376494663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742606 | CGGCCCCCCGACCAG[C/T]CCCTCCCACCTTAGT | 7805 |
| rs376538877 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745122 | ACCCCTCCAATCACC[C/G]CAGGGGAAGAAGGGG | 7805 |
| rs376609258 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756672 | AGCTCTGCCTGCCCT[G/T]CCTGTGACAGGAAGC | 7805 |
| rs376613502 | snp | A/C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747162 | AGGAAACCCATGAGC[A/C/G]TGGCTTTGAGGGGCA | 7805 |
| rs376704636 | snp | G/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732331 | GTGTTTGGGTGTATT[G/T]GTGGGTGTGTGGGGG | 7805 |
| rs376947062 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733552 | TTAGAATGGCCAATC[A/G]TCTAAACAAGTGTCA | 7805 |
| rs377022962 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736231 | GCTAAAAGGGGCAAG[A/C/G]TTCTGTTTCTAGGTT | 7805 |
| rs377424747 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750227 | AGGCCCTGTCATTCT[C/T]CACTTCCTAGATATC | 7805 |
| rs377425364 | snp | G/T | 5.31665e-05 | 0.00515562 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757769 | CGTCCCCTCCTCTGA[G/T]ACACTGAAGGGGAAA | 7805 |
| rs377478565 | in-del | -/CC | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732700 | CCCCAGCTGCCACAA[-/CC]CCGCCATGACCCCAG | 7805 |
| rs377540209 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736098 | GGGGTCTGCGGAGGG[A/G]TCCTGCAGTAGAGAG | 7805 |
| rs377588590 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756676 | GTCTGCTTCCTGTCA[C/T]AGGCAGGGCAGGCAG | 7805 |
| rs377666324 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747006 | GCCACTGACCCTGGC[A/G]TGCCGGTGTCACAGT | 7805 |
| rs377713716 | in-del | -/GTG | 0.485392 | 0.0842056 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732360 | GGTGGGTGTGAGTGT[-/GTG]GAGGGGTGTGGGTGT | 7805 |
| rs386366617 | in-del | -/TTTT | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743796 | GCTGACTGTGTGGGT[-/TTTT]TTTTTTTTTTTTTTT | 7805 |
| rs386366618 | in-del | -/TTTT | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743814 | TTTTTTTTTTTTTTT[-/TTTT]TTTAGCTCAGACACA | 7805 |
| rs397724042 | in-del | -/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753097 | TACTTTTTTTTTTTT[-/T]CCAATTTAAAAGTAG | 7805 |
| rs397815167 | in-del | -/A | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751746 | CAGTCTCAAAAAAAA[-/A]GGGGCGGGGGGCCTT | 7805 |
| rs397840856 | in-del | -/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742219 | TTACCAGCTGGTGGG[-/G]ATTTGCAAAGTGCCA | 7805 |
| rs397970960 | in-del | -/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752831 | ACCTTTTTTTTTTTT[-/T]AAAGAGTCTCACTCT | 7805 |
| rs527265734 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758907 | CAAGCTTCTAGTGCA[G/T]AGCAGACAGGAACTG | 7805 |
| rs527309161 | in-del | -/TGAA | 0.0228947 | 0.104514 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743299 | AGCTGTTGTATTTGT[-/TGAA]TGAATGAATGAATGA | 7805 |
| rs527332980 | snp | G/T | 0.00120024 | 0.0244679 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752684 | TTCCTTGGCAGACTG[G/T]CCCCTCAAGGGCAGA | 7805 |
| rs527438194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737544 | GCTTGGCATGGGCAG[G/T]CCTGGGCCCAGCACA | 7805 |
| rs527515308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742826 | GCAAGATGGGGATAA[A/T]ACTAGTAACTTCCTT | 7805 |
| rs527537693 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750906 | GCCCCTGTGCAGGGC[A/T]GAGGCAGTGCAGCTC | 7805 |
| rs527543036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748191 | GAGCACACACCCGTG[C/T]CAGCCAGAGTGTGGA | 7805 |
| rs527543123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753323 | ATCAAACTTGAGTTG[C/G]TTGGAGCAGCATAGT | 7805 |
| rs527634431 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756114 | GTTAGTGGCAGGGCT[A/G]GGGTGAGGACCCAGG | 7805 |
| rs527738294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743253 | TAGGTTCCAGGCAGG[A/G]AAAGCCTGTATGTCT | 7805 |
| rs527799924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738261 | TAACAGAATGTGGCA[A/G]AAGTGATAGAAGTCT | 7805 |
| rs528034130 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746339 | GGGCCAGCACCCTGC[C/G]CCTCAGAAGGCCCTC | 7805 |
| rs528125743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745050 | GAGACCTCTACTAAT[A/C]CTCAACTCCCCCTAC | 7805 |
| rs528189679 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749257 | AAAAGAACACGCGCT[A/G]CAGAATTTCATTTCT | 7805 |
| rs528215860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744398 | ATGACAGCTCCGTCC[A/G]GCACAGAACGGGGTG | 7805 |
| rs528372790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739693 | CAAGACACCAGCCAG[A/G]AAGAGGGCTCCTACC | 7805 |
| rs528459147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756364 | GACAGCAGGTGCCAT[A/G]TCTGATGCACAACGA | 7805 |
| rs528746256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750578 | CAGGTAAAATTGAAA[C/T]CAGCTCTTTACACAT | 7805 |
| rs528874455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754482 | TCAAGGCTGCAGTGA[A/G]CTGTGATGGCACCAC | 7805 |
| rs528960253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753995 | CTAGAACCCAAATAC[A/G]TTTCCTCCTCGCCCA | 7805 |
| rs529111681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739606 | CATAAGGCAGGCTGA[A/T]GAGATGTGATTGCAG | 7805 |
| rs529126545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744157 | GGAGCACGGTGCATG[A/C]TCTAACTGCCCCCTC | 7805 |
| rs529164073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739286 | CTCCCGGGCCAGGGC[C/T]CTTCCATGATGTAGC | 7805 |
| rs529252614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755769 | GAGATTTTTTTCTAC[C/T]ATGCATCAATCACTA | 7805 |
| rs529423130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750320 | AGAGCAAAGACCCAC[A/C]ATAGTGATAATAAGT | 7805 |
| rs529507329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756327 | GAGTCCTTGAATCTG[A/G]CAACTTGACTCCAAG | 7805 |
| rs529711696 | snp | A/C | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740421 | CACCCCCCACTCCCC[A/C]CCACGCCCCGCATAC | 7805 |
| rs529830018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734416 | GCCTTTTTGCCACCA[A/C]AAGGGATGGGCTTCC | 7805 |
| rs529835726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757211 | CCCTCCAGGCCCCAG[A/G]GGAAGAATCGGGGCT | 7805 |
| rs529899983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757568 | GAGCAGGAGTTCTTT[C/G]ATTTGTGGGGCTCCG | 7805 |
| rs530079879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741494 | GAAACATGGTTCTCC[A/G]AAAGGTATGTGTGAA | 7805 |
| rs530095342 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751638 | CAGCTACTTGGGAGG[C/G]TGAGGCACAAGAATC | 7805 |
| rs530157165 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747450 | AGGCTCAGGCTGCGG[C/T]CCCAGCCATGCTCAG | 7805 |
| rs530373853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741916 | AGCACAGGAGGATGC[A/G]ACAGAGGGTGCTGGG | 7805 |
| rs530433119 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751000 | CCCTGGGAAACCAAC[A/G]CTCGCCTCACAGTGA | 7805 |
| rs530556283 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740331 | TAGGAGTGAACAGGA[A/G]GGAGGGGCGGGGCAC | 7805 |
| rs530563188 | snp | C/T | 0.000183402 | 0.00957431 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733618 | AATTATGGAGAGACC[C/T]GAGGAGTGACTCAGC | 7805 |
| rs530575564 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749313 | ATAGAACTACATAGA[C/T]AGGCAGAAGTCAGTG | 7805 |
| rs530580883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745279 | CCCAAGGCCTCCCAG[A/C]TGGTCATATGCAGGG | 7805 |
| rs530645439 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739733 | CTGAGCACAGGGCCC[A/G]TGTCTGGTCCCCTCC | 7805 |
| rs530790598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750621 | TCTCAGAACAAGGCT[C/T]TGGGGATGGCAGAGC | 7805 |
| rs530975262 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750914 | GCAGGGCTGAGGCAG[G/T]GCAGCTCATGGCTTT | 7805 |
| rs530993109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757170 | GGGGAGATCCCCACT[C/T]CTCATCCCCTCGAGT | 7805 |
| rs531062026 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740819 | TGAGTGTTAGCAAGG[A/G/T]GAGTGGGTGCTGGCA | 7805 |
| rs531189457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746825 | CTGACCTGCCTCACA[A/G]GATTGCTGAGGTCAA | 7805 |
| rs531381550 | in-del | -/GTGA | 0.00398564 | 0.0444627 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732208 | AGGGGTGTGGGGGGT[-/GTGA]GTGTGTGGGTATATG | 7805 |
| rs531383729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752511 | TCATGCTACTCCCCC[C/G]GCCCAGCGTGACCTC | 7805 |
| rs531387104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747641 | ATTTGTTTCTTTTCC[G/T]GGTGGCTCTGAGGAG | 7805 |
| rs531469337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751857 | CACTTTTGAGGCAGG[A/G]ACCACTGGCCCCATT | 7805 |
| rs531574609 | snp | A/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747044 | GAACTCGATACATGA[A/T]TGGTGTGCTCAGAGC | 7805 |
| rs531662462 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748667 | CCCAGATACCACCAG[A/C/G]CGCCCCCATTCCTGG | 7805 |
| rs531767765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737768 | AGCACCCACACATCC[A/G]GGAATAATGATCCCA | 7805 |
| rs532241712 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743890 | TGGAAAGGGACTGAA[C/T]GGAAGAGTGATGAAG | 7805 |
| rs532243663 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735497 | CAAGGGGATTTGGGG[A/G]GCTTCTAGCCCACCC | 7805 |
| rs532274952 | snp | A/G | 5.9489e-05 | 0.00545353 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757642 | CACGCACACACACCC[A/G]GGGCCCGCACACTCA | 7805 |
| rs532318394 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758247 | GAGGCATTTCCTGCC[C/T]CTTCCAGGCATGCTC | 7805 |
| rs532379792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751732 | TGATAGAGCAAGACT[C/T]AGTCTCAAAAAAAAG | 7805 |
| rs532607783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747552 | TATTCCCGTCTGCAC[G/T]CAGCCTTTCTTTCTT | 7805 |
| rs532672492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748088 | CCTGAGGCCCAGGAC[C/T]CACCGTCTCAGAAGC | 7805 |
| rs532835800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753853 | GAGGAACTAGGCATG[C/G]GGGACGCAAGAACTA | 7805 |
| rs532990176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748697 | GGGCCACGCACTCCG[A/C]AGCAGCCCGGCCTGG | 7805 |
| rs533025975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740354 | CGGGGCACTGGAGGC[A/G]GAAAGACCAACATGA | 7805 |
| rs533108108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742349 | CCAGAGGTCATCCAT[C/T]GTCCATGGAGAGGTG | 7805 |
| rs533115387 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734664 | GTAAGTTACCAGGAA[C/T]TTAAACCGTCACTTT | 7805 |
| rs533217276 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758815 | CCATATTGCAATAAA[A/G]AAAGGGAATAGGAAG | 7805 |
| rs533251102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739194 | CTCTCGTCCCCTGTG[A/C]ACAGAGAGACATGAA | 7805 |
| rs533406351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749820 | CAAGACGTTCCTCTT[A/G]GTAAACTGTGATTTG | 7805 |
| rs533427333 | in-del | -/AGAC | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749310 | ATTATAGAACTACAT[-/AGAC]AGGCAGAAGTCAGTG | 7805 |
| rs533531119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747035 | GTCTCCAGGGAACTC[A/G]ATACATGAATGGTGT | 7805 |
| rs533548771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749497 | ACATCAAGAAAAGGT[C/T]TGCAAAAATCAAATA | 7805 |
| rs533590453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747708 | GCTGGAGGATGGAAA[C/T]CAGGGAAGATGGGGA | 7805 |
| rs533643393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754846 | CCAAGTCCACAAATA[A/G]CTCATGATGTGCAGA | 7805 |
| rs533971678 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753814 | CAACAAACGCACCAC[A/G]CTAACGTTGAGACGT | 7805 |
| rs534051692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742082 | TGTGGGGTGGAGAAT[C/T]GCAGGGAGATGCTGT | 7805 |
| rs534180728 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759544 | AACACACTGACAGCA[C/T]GTGGAATAATTGTAC | 7805 |
| rs534355219 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732023 | GGGAGTGGAGTGCAC[A/G]CCTGATTAGGGAGAC | 7805 |
| rs534360773 | snp | C/T | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743358 | CTCTCAGATGACCCT[C/T]GCTAAGAATGATGTG | 7805 |
| rs534439389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743027 | GATCAGAGAGCACCA[C/T]AGAGCTTCAGGTTCC | 7805 |
| rs534673841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737949 | CCAGGCTGGCGCACC[A/G]GCCCATCCCCAGCTG | 7805 |
| rs534679732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749976 | ATGCAGGAGATGTGA[C/T]GGCTCATGCAAAACC | 7805 |
| rs534764868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749609 | CAGGCCAGAGGGCAC[A/G]ACTCCCAGGGACCCA | 7805 |
| rs534967531 | snp | C/G/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739861 | AGCTCAATGTAGGAG[C/G/T]CCAGCAGGGTGAGCA | 7805 |
| rs534967889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741132 | GAAGGCCCATCTTCC[C/T]CAATCAGATCATGAG | 7805 |
| rs535029927 | snp | C/T | 1.81e-05 | 0.00300827 | stop-lost | LAPTM5 | GRCh38.p7 | 1:30733828 | GGGGCCTGGCGAGGG[C/T]CACACCTCTGAGTAT | 7805 |
| rs535063622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737464 | GAGCTGGCATGGGAA[A/G]GCAAGAGAAAGGAGC | 7805 |
| rs535165609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748706 | ACTCCGCAGCAGCCC[A/G]GCCTGGCTGCCTGCA | 7805 |
| rs535254913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734443 | TTCCGGAAAATGAAG[C/G]CAACATCAAGGAAAG | 7805 |
| rs535377609 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30731989 | CTTCCCCAGTGTCCA[C/G]AGCAGGACCCAGCCC | 7805 |
| rs535379954 | snp | A/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741183 | GCGTAGGTCCCCCTC[A/T]GGGTGCTGGCTCCTG | 7805 |
| rs535459514 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749547 | TGTGCCAGGTTCCAC[A/G]GGATCATGAAGATGA | 7805 |
| rs535528199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754219 | GACAAAAAGCCAGGA[A/C]CCAAGAGACCCAATT | 7805 |
| rs536027010 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745348 | GCATCTTCCAGCCAC[A/C]CGGGCTCTGCCTAAG | 7805 |
| rs536104191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746050 | TGCCCACCCTTCCCT[G/T]GCAACCAAGCCCCAG | 7805 |
| rs536306838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740495 | ACAGTAAGAGGCCCT[A/G]CCAGGAAGAGGCTGA | 7805 |
| rs536309221 | snp | A/G | 0.000492409 | 0.0156832 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733705 | GCGAGGGAGACACAA[A/G]CAGATTGTCCTGCCA | 7805 |
| rs536498776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750744 | CAGGCTGCAGAGTCA[C/T]TTGCCCTCCTGAGCC | 7805 |
| rs536499412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735759 | ATGCAAGTTAATGTA[A/G]GAATTGGGCAGAAGC | 7805 |
| rs536522987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756588 | GATTTGCATGCAGGA[A/G]TCTGCATCCAGAGGC | 7805 |
| rs536688343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735642 | ATGTTTTCTTCAAAA[C/T]TGCTTCCGATATGTT | 7805 |
| rs536709963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746594 | GCTTCTCTCCCCCAA[C/T]AATGCGCAGGCAGAC | 7805 |
| rs536859245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750012 | AACCTAGACTCGGAC[A/G]GCTCAGATGGCGCTG | 7805 |
| rs536888248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746968 | CTCTGAGCACCTACC[A/G]CCTCCAAACTCTGTC | 7805 |
| rs537085418 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740450 | ACAATTGGACCTTCC[C/T]CCACCAGCCACTCCC | 7805 |
| rs537100656 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732091 | GACAGCATTGGGTCA[A/G]GACCACCCCTCGCTC | 7805 |
| rs537113444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745501 | GTGAAAACCACCTGC[A/G]TTTAAAACCCAGGCT | 7805 |
| rs537236146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756110 | GCCAGTTAGTGGCAG[A/G]GCTGGGGTGAGGACC | 7805 |
| rs537300539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734565 | TGAGCTAGTAAATTC[C/T]TGAAGTCAGATTGAG | 7805 |
| rs537360651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735107 | GTCCAGAGAGGGAAG[A/G]AAACTTGACCCAAAT | 7805 |
| rs537369191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755250 | CAAGTGGCAGGGTAG[G/T]GAGATGGGCAGTGCT | 7805 |
| rs537430688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745912 | GGAGGCTGAGAGAGA[A/C]CTCACATGTCCTGTG | 7805 |
| rs537448774 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746671 | CACTGTCCCTTCATT[C/G]TATGCTGGTGAGATC | 7805 |
| rs537520661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750425 | CACGGGCTCTGCATC[C/T]GAGTATTTTCAATCT | 7805 |
| rs537595264 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732219 | GGGTGTGAGTGTGTG[A/G]GTATATGGGGGGTGT | 7805 |
| rs537824604 | snp | A/C | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751550 | TCAAGACCAGCCTGG[A/C]CAACATGGTGAAACC | 7805 |
| rs537923550 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754477 | GGAGTTCAAGGCTGC[A/G]GTGAGCTGTGATGGC | 7805 |
| rs538080063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736070 | GGGGAGCTGGGGGAC[A/G]GAGCTGTGTGCTGGG | 7805 |
| rs538089311 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757877 | GGCAGGGACAAGGTC[A/G]TCACAGCTGGGGCGG | 7805 |
| rs538106132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746935 | CCTCTGGGCATTCAC[C/T]GACTCTCAGTAAACA | 7805 |
| rs538637399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757235 | CGGGGCTGTGTCTGC[A/G]GCCGACCTCACATCC | 7805 |
| rs538718242 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738410 | AGGCAAAGAGCCCAC[A/G]CCCTGTGAGTGAGCC | 7805 |
| rs538720201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735319 | GTCCTTCTCACGCTC[C/T]AGCAGGCCTAGGACA | 7805 |
| rs538881588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746883 | GCACACAGCAGGTGC[A/C]CCATAAACAAGCACA | 7805 |
| rs538883638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741005 | GGGGACCCAGGGACC[A/G]CGGGTTCCTCTTCTG | 7805 |
| rs538896371 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750790 | AAAATGGAGGCCCCC[A/G]TGGCAGCTGCCATTT | 7805 |
| rs539047289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748344 | CCATATGGGTCCCAA[C/G]TGCCAGAGCCCTCCC | 7805 |
| rs539145440 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756419 | CAGGCGTGGTTCTGC[A/C]TGCTTTGTATGTATC | 7805 |
| rs539147511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736012 | AGAGGCAGAATGAGG[A/G]TCAAAGAGGGAAGCC | 7805 |
| rs539227791 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758468 | TCTCTCCCACTTCCT[C/T]ACCCTGAGCCGCAGG | 7805 |
| rs539309193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737417 | ACATGCCCTAAATGG[A/G]CTGTCTCGGAGGATC | 7805 |
| rs539370764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737835 | GTCACCTTGGTCGAC[C/T]GCCACAGCAGCCTTA | 7805 |
| rs539414490 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736213 | TCAGTCCTTGGAGAA[G/T]ATGCTAAAAGGGGCA | 7805 |
| rs539596515 | in-del | -/A | 0.00914312 | 0.0669923 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733354 | CATATATTTATATAT[-/A]GGGGGTAACTAATTA | 7805 |
| rs539745250 | snp | C/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732564 | TTGCAGAGCCTTCTC[C/T]CTCTGTACCCCCCGA | 7805 |
| rs539813383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753687 | AGACTAAATGTAACG[C/T]GGCATCCTGGATGCA | 7805 |
| rs539825040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748782 | TCTCGTCCTCACCCG[C/T]CGCCTCCACCTCATC | 7805 |
| rs539887025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743120 | CCATGGCCCCTCAGG[A/G]AACAATAACATCTTC | 7805 |
| rs539910693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746700 | TCATGAAGATAAGAG[C/T]TCGGGTGCTGGGGTC | 7805 |
| rs540016063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743656 | AAAACTGTCCCCTCC[C/G]CTCTAGTCGGTGCCC | 7805 |
| rs540079705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738775 | TCACTCCTGACAAGT[G/T]TCTTCCTGAGAGGGC | 7805 |
| rs540111312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736225 | GAAGATGCTAAAAGG[A/G]GCAAGGTTCTGTTTC | 7805 |
| rs540240101 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755108 | CAACCTGGGCCGAGC[A/G]CACAGCTTCCAGGAC | 7805 |
| rs540268973 | snp | A/C | 0.133777 | 0.221342 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735421 | GGTTGGGGGTTCCTC[A/C]CCAGCCAGTCCAGAA | 7805 |
| rs540442071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757893 | TCACAGCTGGGGCGG[A/G]GCAGCTGGGGAGGGG | 7805 |
| rs540518918 | snp | C/T | 6.69568e-05 | 0.00578567 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737582 | CACCCCTCCCAGAGC[C/T]GCAGGGCAGGGATCC | 7805 |
| rs540639325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747940 | AGTGATGGGGGTGAC[A/G]GCAATGGGGACATCA | 7805 |
| rs540764941 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751674 | AACCCGGGAGGCAGA[C/G]GTTGCAGTGAGCCAG | 7805 |
| rs540808577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737215 | TACATTTTGATGCCT[A/G]AATTACATAAAACTG | 7805 |
| rs540823839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749002 | ATTCAGAAAGATCAA[A/C]TGAGCAGCACAGGTG | 7805 |
| rs540836362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743319 | TGAATGAATGAATGA[A/G]TGAATGAACAAATGA | 7805 |
| rs540922487 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752989 | TTTTTTGTATTTTTA[A/G]TAAAGACAGGGTTTT | 7805 |
| rs540976437 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759699 | CTCATTTTAAAAGAA[A/G]TGCATTTAAATAAAA | 7805 |
| rs541052252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739126 | TCCCAGTTACTGAGC[A/G]GCACATAGTAGGCCC | 7805 |
| rs541115940 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732465 | GAAACACATCAGCCA[C/G]ACAGAAGCTTGTTGC | 7805 |
| rs541197276 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738543 | CAGCTAAGCCACTCC[C/T]AAGCTCCTGATCCTC | 7805 |
| rs541280991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755468 | TGTCCCTGTAGAAGC[C/T]GAACACATACGCCAT | 7805 |
| rs541466069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739490 | CTGGGGGCTAAAAAG[C/T]GCACATGTCCTTTCC | 7805 |
| rs541490355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736977 | AACGCTCAGGTCTTT[A/G]TTGGGTTTTGTGGGG | 7805 |
| rs541621360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753293 | CTCAAGGAGGTGGGG[C/T]GGAACTCCCCATTCA | 7805 |
| rs541670654 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733137 | TTTGAATTAACAATT[A/C]TACAGCCACTCAGAG | 7805 |
| rs541759204 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759565 | ATAATTGTACATGGT[C/G]TATGGGTAAACATTT | 7805 |
| rs541912238 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755939 | GGCTCCCGGGGTCAC[C/T]GCAGGCCCCATCTGC | 7805 |
| rs542022863 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758368 | GAGGGGGAATGATTC[A/G]TGCAAGGTCACACAG | 7805 |
| rs542279692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742723 | TTACACACAGAGAGC[C/G]CATGTTCAGAATCCT | 7805 |
| rs542439805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739616 | GCTGATGAGATGTGA[C/T]TGCAGGTACATTCCA | 7805 |
| rs542527633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744968 | AAATTATATGATGGA[A/C]AAATTTAGAAATTTT | 7805 |
| rs542644936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755355 | AGAATTATCCAGCCC[A/G]AAATATCAATGGTGC | 7805 |
| rs542645064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749421 | CATGGGTGTGTTCAC[C/T]TTGTAGAAGCCCACC | 7805 |
| rs542668390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733997 | TCATGGGACCCAAAC[C/T]CCCACCTCTGGCAAA | 7805 |
| rs542771460 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751842 | TCTCCTCCAAATGAT[C/T]ACTTTTGAGGCAGGG | 7805 |
| rs542791072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745563 | CCCTGCGGCAGGGGA[A/C]GAGGGAGGACTTTGT | 7805 |
| rs542823696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750872 | TTGAGGCTGGGGGAC[A/G]GGTGCCTTGTCCCAA | 7805 |
| rs542851085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757364 | GCTGCTGTGCCCCAT[C/G]TCACAGAGGCAGAAA | 7805 |
| rs542852834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740105 | GGGACAGGGAGTGGA[C/T]AAGACCCAGGCCCTG | 7805 |
| rs543205874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744129 | AAGCTTACGTGGTTC[A/G]GCAGTAGTACCAGGA | 7805 |
| rs543329213 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748762 | CCTCTTCACTCTTCC[A/G]CAGTTCTCGTCCTCA | 7805 |
| rs543338484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757033 | AACAAGAGCTTGGGC[C/T]GGACAAGTTACCCTA | 7805 |
| rs543389078 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733188 | GGCATCCAGTTGATG[C/G]GTTCATTTGAATTAA | 7805 |
| rs543415346 | in-del | -/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737256 | AAAACAAGACTCCTG[-/C]CCCTGAGGCCCAGAG | 7805 |
| rs543450677 | snp | A/G/T | 6.97671e-05 | 0.00590588 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733912 | CTCGTAGGACGGCAG[A/G/T]ACCACCTGGGAGAGA | 7805 |
| rs543455307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754391 | AATATTTAAAATTAG[C/T]TGGCCATGGTGGCAT | 7805 |
| rs543475009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739541 | AGCAGCACTGACTGA[A/G]TGCTGACCATGGGCT | 7805 |
| rs543591963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749674 | GGGTCCAACCGTAGG[A/G]GTCAGGGCGGGCTTC | 7805 |
| rs543604139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744810 | GGAGAGGACTTAGAT[A/G]TTTTGATCATGCATC | 7805 |
| rs543621622 | snp | C/T | 0 | 0 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756870 | GGAGTAGGGTGGGTC[C/T]AGGCAGGACAGTACA | 7805 |
| rs544004036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745692 | GCCCCGACCTTCCAC[A/G]AAGATGCCAGGCCCT | 7805 |
| rs544187520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746178 | CCTGGCCTCAGCTTT[C/T]GATTCTGGTCAATGA | 7805 |
| rs544232848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740694 | TCAGGGACCACCTGC[C/T]CCATTTCTCCATTTC | 7805 |
| rs544378750 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739468 | AAAGAAGAAATAATA[C/G]TGGGGGCTGGGGGCT | 7805 |
| rs544398625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735408 | GACCTCTCATTCTGG[C/T]TGGGGGTTCCTCACC | 7805 |
| rs544469741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747867 | CTGTTGGGATGTTGT[C/T]GGAGTTGGCGTGGTG | 7805 |
| rs544484217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742172 | ATGAGCAGCCACTGA[C/T]GGCTTTAAGCAGAAG | 7805 |
| rs544615972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750961 | GGGGGTGCTTTGTGC[A/C]ACTTCCCTTGGCAGG | 7805 |
| rs544917930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747392 | GTCACACACCAAAAC[G/T]GTCGCAGGGTCAAAA | 7805 |
| rs545117502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756258 | TGCTTCTCTCAGCTC[C/T]TGCATTGGCAGGAGC | 7805 |
| rs545210161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740669 | ACAATCTTGACTGAT[A/C]TCAGAGTCTTCAGGG | 7805 |
| rs545288172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740242 | AAGGGCTTTGTGCAC[C/T]TTTTACAGAGGAGAG | 7805 |
| rs545296210 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746083 | CCAGCCACTCAGAGC[C/T]CAGGAGACAAGAGCT | 7805 |
| rs545400971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757417 | GTCAGTTACATTTGC[C/T]TGGAAAGTGGATTCC | 7805 |
| rs545456726 | snp | A/G/T | 0.000238728 | 0.010923 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741649 | CCTCACCTTGACTAC[A/G/T]CCGATCAGTAGGCTC | 7805 |
| rs545543210 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744795 | GCTAGCCTGAACCCC[A/G]GAGAGGACTTAGATA | 7805 |
| rs545610834 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759435 | ACAGAAGCCATTTGA[C/T]GATTTCCTACCATAA | 7805 |
| rs545714335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750903 | GCAGCCCCTGTGCAG[A/G]GCTGAGGCAGTGCAG | 7805 |
| rs545825544 | snp | C/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733586 | CTGATTGAAATAAAC[C/G]AAGCATTGTTGGGCT | 7805 |
| rs545870306 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748611 | CTCAGTGGGGGCCAG[C/T]CCCCCAAGAGCACTA | 7805 |
| rs546215433 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755658 | GACATCGGATGGCAC[A/G]ATCAACAAGAAACCT | 7805 |
| rs546394881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738114 | GATGCAGGGGAACTC[A/G]CCCTAGGTGAGACTG | 7805 |
| rs546436051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757600 | AGATGACGGGTCACC[A/G]CAGACATTCACACTC | 7805 |
| rs546449784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753825 | CCACACTAACGTTGA[G/T]ACGTTAGCAATAGAG | 7805 |
| rs546475626 | snp | C/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757909 | GCAGCTGGGGAGGGG[C/G]AGTGGGGACAGGGCA | 7805 |
| rs546482766 | snp | A/T | 0.000399281 | 0.0141238 | missense | LAPTM5 | GRCh38.p7 | 1:30737624 | AGATAAGGACAGTGA[A/T]GAAGGCGATGGAAAA | 7805 |
| rs546689617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741960 | CTGGGGTCCACTTCA[A/G]CCAGGGTGAGGCTGA | 7805 |
| rs546691254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734424 | GCCACCACAAGGGAT[A/G]GGCTTCCGGAAAATG | 7805 |
| rs546838064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751071 | TCAAAATAAAAGCCT[C/T]ACTTCCTGGAGGCCT | 7805 |
| rs546838155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746599 | TCTCCCCCAACAATG[C/T]GCAGGCAGACAGCAT | 7805 |
| rs546918319 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757213 | CTCCAGGCCCCAGGG[G/T]AAGAATCGGGGCTGT | 7805 |
| rs546953329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736495 | CTGGAGTGCAGTGGC[A/T]TGATTATGGCCCACT | 7805 |
| rs546983382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735867 | GAGGAGAGGGTCCTG[C/T]ACTGGAAGGTCTTGT | 7805 |
| rs546983599 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751908 | CTCAGATAACAAAGG[C/T]GCCCGCCTGCTCAAG | 7805 |
| rs547012185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747459 | CTGCGGTCCCAGCCA[C/T]GCTCAGCCACCCTTC | 7805 |
| rs547033061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752704 | TCAAGGGCAGAGGCC[A/G]TGAATGAGTCAGGGC | 7805 |
| rs547186136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742858 | GGAGGCTACTGTGAG[A/G]AGTAAATGAGACTAT | 7805 |
| rs547217817 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758914 | CTAGTGCAGAGCAGA[A/C]AGGAACTGCCATGAA | 7805 |
| rs547316261 | snp | A/G | 2.24062e-05 | 0.00334703 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742441 | CGCCACTCCACCGGC[A/G]TCCCCTGGACCTACC | 7805 |
| rs547321887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748689 | CATTCCTGGGGCCAC[A/G]CACTCCGCAGCAGCC | 7805 |
| rs547351789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751069 | GCTCAAAATAAAAGC[C/T]TCACTTCCTGGAGGC | 7805 |
| rs547385866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753370 | ATACAGCATGGAAAG[A/G]AGAAAAAAAGAGTAA | 7805 |
| rs547482715 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734284 | TCCCCCTGGCTATAG[G/T]CCTTGGTTTGGGGAT | 7805 |
| rs547744337 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758334 | CCCCATTTTACAGAT[A/G]AAGAAACTGAGGCAC | 7805 |
| rs547749928 | snp | C/T | 3.47596e-05 | 0.00416877 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739933 | AGCAGGTACTTCTCC[C/T]GGTTCTGAAAGGTAG | 7805 |
| rs547806645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751967 | GCCTGTGTTCCTTTC[A/G]ATCACAAATCACTGC | 7805 |
| rs547841577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738268 | ATGTGGCAGAAGTGA[C/T]AGAAGTCTTAAAAGA | 7805 |
| rs547930362 | snp | A/G | 1.68957e-05 | 0.00290647 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30757704 | GATGCGGACATTGAA[A/G]CAGCAGCAGGTCTGG | 7805 |
| rs548090365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742366 | TCCATGGAGAGGTGG[C/T]AGTGCCTCCAACACT | 7805 |
| rs548115833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752533 | CGTGACCTCTTTTCC[A/C]AGGTGCCCAAGCAAA | 7805 |
| rs548360430 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742045 | GGACAGGGTTGGTGA[A/G]GTCAGTGTGGCTGGA | 7805 |
| rs548397660 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749912 | ACACACGGATCCACC[A/G]GTTTGGCAGGGGTGG | 7805 |
| rs548424896 | snp | A/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753642 | AAATCTGAGAAACCA[A/T]CATACCAAGAGGAAC | 7805 |
| rs548457500 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737363 | TAATTCCAGACAGCT[A/G]GAATTAGACATCTGA | 7805 |
| rs548586906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737799 | CCCTCCACACACACA[C/G]GAGCACAGCGTGGCA | 7805 |
| rs548663069 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745776 | AGGACATAGGATGGA[G/T]AGGAACTCACATTTA | 7805 |
| rs548701905 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743112 | TCTGTCTCCCATGGC[C/T]CCTCAGGGAACAATA | 7805 |
| rs548708852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738452 | ATCCTTCAGATCTAA[C/T]CAAGCCCTCAGTTGT | 7805 |
| rs548757716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753498 | TGGCACATCATCTCT[A/G]TGGTCTTCCTCCCAA | 7805 |
| rs548812716 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733220 | TGGTTTGGAGGCTAA[C/T]GTGATTTTTTAAATT | 7805 |
| rs548835633 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30731995 | CAGTGTCCAGAGCAG[C/G]ACCCAGCCCCAGGGG | 7805 |
| rs548969498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744190 | CCTGCTAAAGAGTGA[A/G]CTGGAAAGGCTTTGT | 7805 |
| rs549111960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755024 | CCTTTCTGGGAAGGA[A/G]AGAGGACTCTTTCGG | 7805 |
| rs549128710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756337 | ATCTGACAACTTGAC[C/T]CCAAGGATGCTGACA | 7805 |
| rs549229569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739306 | CATGATGTAGCCCCC[C/T]GGTCTCTTCAAGGAC | 7805 |
| rs549299736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750375 | TTATTAGACGCCAGG[C/T]CCTCTTCTGAACTTA | 7805 |
| rs549310638 | snp | A/G | 0.000521574 | 0.0161405 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739820 | TCACAGCACGGCTCC[A/G]GGAGGCCAACTTGAG | 7805 |
| rs549381418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742931 | CTGTTACTACTGAAG[A/G]TCAGGCTTAAAGAGG | 7805 |
| rs549463429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748702 | ACGCACTCCGCAGCA[A/G]CCCGGCCTGGCTGCC | 7805 |
| rs549554188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745803 | TTTATTCAGCACCTA[A/C]TGTGTGCTCAGACCT | 7805 |
| rs549564774 | snp | A/C | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740424 | CCCCCACTCCCCACC[A/C]CGCCCCGCATACAAT | 7805 |
| rs549692090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737886 | GCCCCATCCCACTGA[C/T]GGGCAAACCAAGAAA | 7805 |
| rs549713819 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751116 | CAACAGAGAAGTCTC[A/G]GCCAGGCCAGGCTAG | 7805 |
| rs549764195 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749093 | CCAAGCTGGAATCAA[C/T]CCAAATGTTATTTTG | 7805 |
| rs549786463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754961 | TGCTCAAGGTCCTAT[C/T]AGCACACCTGTTGCC | 7805 |
| rs549838532 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740717 | TCCATTTCTCTAGCT[A/G]AACCCTTTGAGTTTC | 7805 |
| rs550104141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744543 | TTTCAAAGTCTCAAG[A/G]TTCCAGGATTATCTG | 7805 |
| rs550215498 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732565 | TGCAGAGCCTTCTCC[C/T]TCTGTACCCCCCGAC | 7805 |
| rs550242995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749514 | GCAAAAATCAAATAG[A/G]GATTGGCTGGCACCT | 7805 |
| rs550302477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749858 | CCATGTGCTGAATAC[A/G]CAGCAGGCCTCAGTA | 7805 |
| rs550526676 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750450 | CAATCTGCAATCCAC[C/G]ATGTGGAACCTGCGG | 7805 |
| rs550571146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740851 | TTGAGGCAGGGTGGA[C/T]GCATTCCAAACCAGC | 7805 |
| rs550600999 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734372 | TGGGATTTCTGAGAG[G/T]GTGGGATATCTGCCT | 7805 |
| rs550725374 | snp | A/G | 0.000325585 | 0.0127549 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739782 | TGGGCTCTGCTGTCC[A/G]GTGAGAGGTGGGGGC | 7805 |
| rs550758139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756473 | CCCTATCAGATGGGT[A/G]TGATAATTCACATCC | 7805 |
| rs551130054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750706 | CTGGAGCAGACACCT[A/G]GGCTCGGGTTCTTTA | 7805 |
| rs551358350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739707 | GGAAGAGGGCTCCTA[C/T]CCTCCCCAGCCTGAG | 7805 |
| rs551528295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744489 | CAGCTGGGCTTAGAG[A/G]AGGACCATGAGCATC | 7805 |
| rs551547847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740779 | GCAAACGGCCTCCCC[A/G]GGCAGCATGGGTTCC | 7805 |
| rs551603763 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750539 | GACAGGTTCTAACAT[-/G]AGTCCCATATTTTTC | 7805 |
| rs551683693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746490 | TGTCCCCGGTTTCCA[C/T]CTGGACACAGCGCTG | 7805 |
| rs551683759 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740443 | CCCGCATACAATTGG[A/C]CCTTCCTCCACCAGC | 7805 |
| rs551727357 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755663 | CGGATGGCACGATCA[A/G]CAAGAAACCTTAACA | 7805 |
| rs551893704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756402 | AGCACTCACCTGTGC[A/G]TCAGGCGTGGTTCTG | 7805 |
| rs552038183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751820 | CCTCCACCCGGCTTC[A/G]CTAGGGTCTCCTCCA | 7805 |
| rs552159834 | snp | A/C | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752898 | TGCAACCTCCACCTC[A/C]CAGGTTCAAGCAATT | 7805 |
| rs552418680 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757419 | CAGTTACATTTGCCT[A/G]GAAAGTGGATTCCAG | 7805 |
| rs552597813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736552 | GATCCTCCCGCTTCA[A/G]CCTCCCTAGTAGCTG | 7805 |
| rs552735758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742018 | GAGCAATGAGGAATC[A/G]GCCTGAGACAGGGAC | 7805 |
| rs552768359 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759145 | TTGGGCTCCTGGGAG[A/G]CCTGGCCTATCCCTT | 7805 |
| rs552861844 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732797 | CGAACAGATGTGCCT[A/G]ATTTCAGGGCTGAAT | 7805 |
| rs552879897 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737493 | GCTAAAAGCAGGAGA[A/G]GAGGCATGGAGGACA | 7805 |
| rs552896439 | snp | G/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751826 | CCCGGCTTCGCTAGG[G/T]TCTCCTCCAAATGAT | 7805 |
| rs552899878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756227 | TACAGGGTACAGGGA[C/T]ACTCAAAGAGTGATT | 7805 |
| rs553091100 | snp | A/G | 0.000115457 | 0.00759706 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735292 | CCCAGGTCAGGCTGT[A/G]CTTTGCTGAGCGTCC | 7805 |
| rs553118952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750891 | GCCTTGTCCCAAGCA[A/G]CCCCTGTGCAGGGCT | 7805 |
| rs553147219 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740570 | ATTCATTCATATGCT[C/G]TCACAGCTGGGGACA | 7805 |
| rs553156963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746063 | CTGGCAACCAAGCCC[C/G]AGCCCCAGCCACTCA | 7805 |
| rs553226164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740969 | TGGCTATGTGGTGAG[A/G]CCCTGGCTTCCTGCC | 7805 |
| rs553306940 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747765 | GGGCAATAAGGATGG[C/T]GGTACCAGAGGGGAT | 7805 |
| rs553345015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750487 | AGGGCCGACTGACCA[C/T]ACACTCTCTCGTGTC | 7805 |
| rs553401870 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736827 | CCTTCTGTGGTCATC[A/G]GCATCCCTGTGGCTT | 7805 |
| rs553493250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747262 | AGGCCTGGTGGTGCA[A/G]GTGTGTTTCAGTCCC | 7805 |
| rs553551071 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744668 | TTATAAACTCAGAGA[G/T]ATTAGGTGGCTTGCC | 7805 |
| rs553633213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757405 | CTCGGAGTGAACGTC[A/T]GTTACATTTGCCTGG | 7805 |
| rs553743401 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759812 | GAGTAGGTGGCATCC[A/G]TTTGGGAATCCTGGG | 7805 |
| rs553789022 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757456 | TACTCCTCACTCTTG[A/C]GGCATCTCCCCAGGG | 7805 |
| rs553809814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736814 | TTTAAAAGCCCTTCC[A/T]TCTGTGGTCATCAGC | 7805 |
| rs553844714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753130 | TACTTGAGCCACAAA[A/G]TAAAGTACCATTGGA | 7805 |
| rs553864646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735722 | TATAAAGGAGGAACA[A/G]TTAGTACATGTCCAT | 7805 |
| rs553922714 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737396 | GCAGGTGGCCTTTAC[A/G/T]GATTCACATGCCCTA | 7805 |
| rs553949414 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751678 | CGGGAGGCAGAGGTT[A/G]CAGTGAGCCAGGATC | 7805 |
| rs554040759 | in-del | -/C | 0.00478371 | 0.0486721 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752684 | TCCTTGGCAGACTGG[-/C]CCCCTCAAGGGCAGA | 7805 |
| rs554106216 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751286 | GCCTCCTCACCCCTC[A/C]GTGAAGCGCACAGAG | 7805 |
| rs554227071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757339 | TTTGCACACAAATAA[C/T]CTTCCGGCTGCTGCT | 7805 |
| rs554229518 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758793 | CCCTCCTCAGATGAT[A/T]AATTATCCATATTGC | 7805 |
| rs554288301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750861 | CAGGGAGGAAATTGA[A/G]GCTGGGGGACGGGTG | 7805 |
| rs554356945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743044 | GAGCTTCAGGTTCCC[A/G]GAATCATCAACACAG | 7805 |
| rs554425930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753537 | TCCCAGACTAATCAT[A/G]AGAAAACCACCAGAG | 7805 |
| rs554511678 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746674 | TGTCCCTTCATTCTA[C/T]GCTGGTGAGATCATG | 7805 |
| rs554548828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748741 | CCCAGAGCCTGGCTT[C/G]TCTCTCCTCTTCACT | 7805 |
| rs554573100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741080 | GCCTCGGGCCCAGGA[C/G]CCCCTCGTTGTCACA | 7805 |
| rs554598701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741566 | CCCACCCTCTCAGCA[C/T]CCAGCACTGCCCACC | 7805 |
| rs554738181 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758359 | AGGCACAGAGAGGGG[A/G]AATGATTCGTGCAAG | 7805 |
| rs554798940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736092 | TGTGCTGGGGTCTGC[A/G]GAGGGGTCCTGCAGT | 7805 |
| rs554811037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736707 | TCCCAAAGCACTGGG[A/G]TTACAGATGTGAGCC | 7805 |
| rs554876971 | snp | A/C | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740407 | GAGCCCCTCCCCCCC[A/C]CCCCCCACTCCCCAC | 7805 |
| rs554962852 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740893 | GCCCCACTCCTCCGG[C/T]CCTGCAAGGGCCAGG | 7805 |
| rs555110279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753795 | AATATTCATTCACCC[A/G]TTGCAACAAACGCAC | 7805 |
| rs555227958 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759257 | GTGGTTAAGAACTTT[C/G]GCTCCACAGGCCCAT | 7805 |
| rs555300879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749586 | GGGTCAAGACCCAAA[C/T]GAGCATCCAGGCCAG | 7805 |
| rs555487602 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749254 | CACAAAAGAACACGC[A/G]CTGCAGAATTTCATT | 7805 |
| rs555500921 | snp | A/G | 3.67897e-05 | 0.00428877 | synonymous-codon, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739048 | CAGCGTCATCAGGGG[A/G]AACTTGGAGGAGCTC | 7805 |
| rs555832912 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736473 | GATTCTCACTCTGTC[A/G/T]CCTAGGCTGGAGTGC | 7805 |
| rs555881228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742158 | TTTATTCTAGTGTGA[C/T]GAGCAGCCACTGACG | 7805 |
| rs555913564 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759450 | CGATTTCCTACCATA[A/T]TAAATGATAGCCATT | 7805 |
| rs555963874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747819 | GTCACCTGGGAGGCA[C/G]TGGCCATGGTGACCA | 7805 |
| rs556071686 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737447 | CCAAGTAAAGTCAGA[-/G]GGAGCTGGCATGGGA | 7805 |
| rs556099093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754169 | CTTCTGGGGGTGTCC[A/G]CTTTCTACCATCGAC | 7805 |
| rs556140603 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736259 | GTTGGCATTAGGTGA[C/G/T]AGCAGAGACTGCCCA | 7805 |
| rs556245774 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748788 | CCTCACCCGCCGCCT[A/C]CACCTCATCCCCTCC | 7805 |
| rs556263954 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748371 | TCCCTTGCCCCTCCC[A/C]CTCAGGGCTGCTCCA | 7805 |
| rs556429602 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753858 | ACTAGGCATGGGGGA[A/C/T]GCAAGAACTATCTGT | 7805 |
| rs556624797 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757932 | ACAGGGCAGCAGCCT[A/G]CCTCAGAGCACCCCA | 7805 |
| rs556803763 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732175 | TTTACATGGGTGTGT[G/T]GGGGTGGGCGTGTGT | 7805 |
| rs556803927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739456 | CAACTTGGTTCCAAA[A/G]AAGAAATAATACTGG | 7805 |
| rs556931939 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740453 | ATTGGACCTTCCTCC[A/C]CCAGCCACTCCCAGG | 7805 |
| rs556942167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734617 | CCAAAAGTGTCTTAG[C/T]TAATACAATCTCCAC | 7805 |
| rs557064504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739995 | GCCAACACTCCGCCA[C/T]CCAGCCTGATATCCT | 7805 |
| rs557103148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756872 | AGTAGGGTGGGTCTA[C/G]GCAGGACAGTACAAG | 7805 |
| rs557206731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745945 | ACGTGGCCCGGCTGG[C/G]GTGTGAACCCTGTTG | 7805 |
| rs557335154 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732108 | ACCACCCCTCGCTCA[A/G]CATGGCCCATGGGAG | 7805 |
| rs557747360 | snp | C/G | 3.3428e-05 | 0.00408814 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739862 | GCTCAATGTAGGAGC[C/G]CAGCAGGGTGAGCAG | 7805 |
| rs557768518 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754285 | GCCTGTAATCCCAGC[G/T]CGTTGGGAGGCCAAG | 7805 |
| rs557873787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744755 | CCTTCCCATTCCCCT[A/G]ACCCCCAAAATGCCT | 7805 |
| rs557943844 | snp | A/C | | | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738732 | TGCTTCTTTGCTTGG[A/C]TTCCTCCTTTTCTCG | 7805 |