| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs558056175 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741158 | ATGAGCTCTCTGGGG[A/G]CCTTCCAGGGCGTAG | 7805 |
| rs558058802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734547 | TTTGGCTGCTAAGTT[C/T]TGTGAGCTAGTAAAT | 7805 |
| rs558208626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749631 | AGGGACCCAGCACAC[A/G]GGGCTCTGGGTCAAC | 7805 |
| rs558549571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750809 | CAGCTGCCATTTTTC[C/T]GGTGCCACAAATGGT | 7805 |
| rs558621317 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756790 | AAACTGTTAACCACA[A/G]GCCCTGAGTCACCCC | 7805 |
| rs558802659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741533 | GAACGCAGGTGGGAC[C/T]GCCTAACATACCCGC | 7805 |
| rs558849041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752241 | AGCTCCTGCCCCATC[C/T]CTCCATGTGTCCTGG | 7805 |
| rs558998360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749220 | GCTCCCAAACATAAC[A/G]TTGGGAGAAAGAAGT | 7805 |
| rs559034017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745822 | GTGCTCAGACCTGCA[C/T]GCACAGGCTTGCACT | 7805 |
| rs559050595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744360 | AGTTTCACCTTGAAC[A/G]AGAGAAAGAGAAAGG | 7805 |
| rs559122885 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738417 | GAGCCCACGCCCTGT[G/T]AGTGAGCCACCAGGA | 7805 |
| rs559189667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755370 | AAAATATCAATGGTG[C/T]ACTGCAGAGAAGATC | 7805 |
| rs559236215 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740111 | GGGAGTGGATAAGAC[C/T]CAGGCCCTGAATGAG | 7805 |
| rs559250160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751502 | CCAGCACTTTGGGAG[G/T]CTGAGGCTGGTGGAT | 7805 |
| rs559280358 | snp | G/T | 0.000630273 | 0.0177409 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757781 | TGAGACACTGAAGGG[G/T]AAAGAGCCTGGTGCC | 7805 |
| rs559483278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754527 | GGTGACAGAGCAAGA[C/T]CCCATCTCTTAAAAA | 7805 |
| rs559484008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746428 | CGACCTACAGAGTAT[A/G]CAGACAGTCAACATT | 7805 |
| rs559495431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749464 | TAAGATAGCTGTGCT[A/T]TTCTATAGGTAAATT | 7805 |
| rs559639160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739627 | GTGATTGCAGGTACA[G/T]TCCACAGAGGAAGAA | 7805 |
| rs559722940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756351 | CTCCAAGGATGCTGA[C/T]AGCAGGTGCCATGTC | 7805 |
| rs559768912 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742083 | GTGGGGTGGAGAATC[A/G]CAGGGAGATGCTGTC | 7805 |
| rs559846436 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743664 | CCCCTCCCCTCTAGT[C/T]GGTGCCCTATCTCTA | 7805 |
| rs559846654 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735463 | TTGCCCTTTTCATTG[C/G]CCCACAGATACCACA | 7805 |
| rs560027044 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741254 | TTCTTCGGCTCCTCT[C/G]ATCCATTACAAAATC | 7805 |
| rs560090938 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748688 | CCATTCCTGGGGCCA[C/T]GCACTCCGCAGCAGC | 7805 |
| rs560116897 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758078 | GAAGAACACTACCAA[C/T]TTTGGAAGCCAGGAC | 7805 |
| rs560482303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741969 | ACTTCAGCCAGGGTG[A/G]GGCTGAGGAAGGCAT | 7805 |
| rs560569555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747524 | TCTTCTGCCCATCTT[C/T]GGTTTCAGTTCTTAT | 7805 |
| rs560636943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752439 | CCCTCCTAACCCAGC[C/T]TGACAAACCTGCTAG | 7805 |
| rs560804640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742639 | TGTACAGCAGGGAAG[C/T]CAGTAGTGGGGATCC | 7805 |
| rs561014265 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740380 | CATGAGTGAAGGCCC[A/G]GAGGCAGCAGAGAGC | 7805 |
| rs561106487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736471 | GAGATTCTCACTCTG[C/T]CGCCTAGGCTGGAGT | 7805 |
| rs561203417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735412 | TCTCATTCTGGTTGG[A/G]GGTTCCTCACCAGCC | 7805 |
| rs561236549 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751596 | ATACAAAACTTAGCC[A/G]GGCATGATGGCACAC | 7805 |
| rs561394776 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750970 | TTGTGCCACTTCCCT[C/T]GGCAGGGTGGGGTCC | 7805 |
| rs561407415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747416 | GTCAAAATCAGCTCT[A/G]TCCTCCTGCCTCCAA | 7805 |
| rs561472971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741899 | AGCAGAACATCACAC[A/G]TAGCACAGGAGGATG | 7805 |
| rs561493018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742173 | TGAGCAGCCACTGAC[A/G]GCTTTAAGCAGAAGA | 7805 |
| rs561512156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748669 | CAGATACCACCAGAC[A/G]CCCCCATTCCTGGGG | 7805 |
| rs561560173 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758906 | CCAAGCTTCTAGTGC[A/T]GAGCAGACAGGAACT | 7805 |
| rs561856596 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755976 | CTGTCACTCACATGG[A/C]CTGCCCAGACCCTAG | 7805 |
| rs561938251 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739692 | TCAAGACACCAGCCA[A/G]GAAGAGGGCTCCTAC | 7805 |
| rs562009437 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759605 | TATGGTGATAAATTC[A/T]TTTTAATGTGCATTA | 7805 |
| rs562011246 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750750 | GCAGAGTCACTTGCC[C/T]TCCTGAGCCTGTTTC | 7805 |
| rs562020010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742819 | CCCATCTGCAAGATG[A/G]GGATAATACTAGTAA | 7805 |
| rs562081310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737800 | CCTCCACACACACAC[A/G]AGCACAGCGTGGCAC | 7805 |
| rs562275884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736301 | GGAAGCAGGAGCTGG[A/G]GTCTGCAGATGCCCA | 7805 |
| rs562293104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734089 | GAGATAGGTGCAGTT[C/T]CCAGCCCTGTAGTGG | 7805 |
| rs562437815 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758307 | ATCCTTTGAGAGAGG[C/T]ACTATTATGATCCCC | 7805 |
| rs562453877 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758879 | ATTCCACAGCTGAGC[C/T]CCTTTGCAATGCCAA | 7805 |
| rs562516583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752506 | CTGTGTCATGCTACT[A/C]CCCCCGCCCAGCGTG | 7805 |
| rs562722751 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746179 | CTGGCCTCAGCTTTC[A/G]ATTCTGGTCAATGAG | 7805 |
| rs562828629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748138 | ATCTGAGATTTTCAG[A/G]GAGGTAAAGGTTATA | 7805 |
| rs562987539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753177 | ACAGTAAAGATCCCT[A/G]GGTCCCTGTAATATA | 7805 |
| rs563014133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742317 | ACAGCTGAGGCCCCA[A/G]GAAAGGAAGACACTT | 7805 |
| rs563162559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739557 | TGCTGACCATGGGCT[A/G]CACCCCCAATGTGTG | 7805 |
| rs563320463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745464 | AGCCCCAGCACCAGG[C/T]ACCAGAGGTATTTCT | 7805 |
| rs563367621 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742765 | TCTCCAGCTATGTGA[A/C]CCTGGGCAAGCTACT | 7805 |
| rs563510879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750296 | ACCATCACTTCTCCC[A/T]TTATCTTCAGAGCAA | 7805 |
| rs563634726 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755721 | GCCTCTGGGCCCACA[A/C/G]AACCTGCAAATGGAT | 7805 |
| rs563648332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756306 | GAGTTCCTCCTCCCA[A/G]AACTAGAGTCCTTGA | 7805 |
| rs563681615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737299 | CTGAAGACCAACCAC[A/G]CAGCTAGTGACAGTG | 7805 |
| rs563905941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743361 | TCAGATGACCCTTGC[C/T]AAGAATGATGTGGAA | 7805 |
| rs564040288 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759803 | CTGGAGGTGGAGTAG[C/G]TGGCATCCGTTTGGG | 7805 |
| rs564089907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749299 | CAGATGTATGTATTA[C/T]AGAACTACATAGACA | 7805 |
| rs564192091 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736938 | TCAGGTCCCCCTTGA[A/G]TCCTCTATTTTCCAT | 7805 |
| rs564325253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745324 | TTGGCCAATTCCCTC[A/C]GCTGCCCGGCATCTT | 7805 |
| rs564396004 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753852 | AGAGGAACTAGGCAT[G/T]GGGGACGCAAGAACT | 7805 |
| rs564402868 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738322 | CTCTTACATCACTCC[C/T]GCAGGGGAAGCCAGC | 7805 |
| rs564413556 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742218 | TTTACCAGCTGGTGG[A/G]GATTTGCAAAGTGCC | 7805 |
| rs564458693 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732469 | CACATCAGCCAGACA[A/G]AAGCTTGTTGCTGCT | 7805 |
| rs564483751 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758585 | TGTGCGCCAGGCCCT[A/G]GGCTAGGCTTCTCTT | 7805 |
| rs564645442 | snp | A/G | 0.000201066 | 0.0100246 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739156 | CTCACTTGAGAGACC[A/G]TCTCAGCTACAGACA | 7805 |
| rs564675345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755478 | GAAGCCGAACACATA[C/T]GCCATTGCTCACCTG | 7805 |
| rs564832263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750176 | CTTTAGGAGCAGCCA[A/G]TGGGGGGCTCAGAGT | 7805 |
| rs564977538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749811 | AGGAAACGGCAAGAC[A/G]TTCCTCTTAGTAAAC | 7805 |
| rs565032134 | snp | A/C | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750641 | GATGGCAGAGCTGAC[A/C]CCCTCCCCCATCCCA | 7805 |
| rs565096754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741392 | TCTCACCAAAGTGTC[A/G]GTGACCAGCATAGCC | 7805 |
| rs565156702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735628 | GCTGATGGTGGGACA[C/T]GTTTTCTTCAAAATT | 7805 |
| rs565219870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740676 | TGACTGATCTCAGAG[C/T]CTTCAGGGACCACCT | 7805 |
| rs565226363 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734141 | CAGCATCAAGTCCCC[C/G]TTATTTTGAAAACAG | 7805 |
| rs565256971 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750619 | CTTCTCAGAACAAGG[C/T]TCTGGGGATGGCAGA | 7805 |
| rs565437686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747365 | CCAGAGAGAGACAGC[A/G]ACCAGCCCAAGGTCA | 7805 |
| rs565487111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746816 | GGATAATCACTGACC[G/T]GCCTCACAGGATTGC | 7805 |
| rs565631511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742995 | CTGCATCCCCTTCTG[C/T]AACAACAAGCTCTGG | 7805 |
| rs565678419 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732754 | GGGTTGCCTGCTTTG[A/C]CTGAACTAACCTGTG | 7805 |
| rs565762513 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749951 | GGGTTAGAGAGAAAG[C/G]GGAAAGAGCATGCAG | 7805 |
| rs565767851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743608 | GACATACATACAGTT[C/G]TCCAGGTAACCTCTG | 7805 |
| rs565851256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749608 | CCAGGCCAGAGGGCA[C/T]GACTCCCAGGGACCC | 7805 |
| rs566025200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745412 | CAGAGAGGCGCCCCC[A/G]TCCCCTCTCCCTCTG | 7805 |
| rs566108352 | snp | C/G | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740426 | CCCACTCCCCACCAC[C/G]CCCCGCATACAATTG | 7805 |
| rs566117625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755055 | GGTGCAGGAAGATAA[C/T]CCCCCACTGGAGTCA | 7805 |
| rs566380280 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740852 | TGAGGCAGGGTGGAC[A/G]CATTCCAAACCAGCA | 7805 |
| rs566423741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734431 | CAAGGGATGGGCTTC[C/T]GGAAAATGAAGCCAA | 7805 |
| rs566602268 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757221 | CCCAGGGGAAGAATC[A/C/G]GGGCTGTGTCTGCGG | 7805 |
| rs566720319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752420 | CGACACACCTCGTGG[C/T]CACCCCTCCTAACCC | 7805 |
| rs566787565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750789 | TAAAATGGAGGCCCC[C/T]GTGGCAGCTGCCATT | 7805 |
| rs566948751 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741004 | TGGGGACCCAGGGAC[C/T]GCGGGTTCCTCTTCT | 7805 |
| rs566960554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746877 | AGCCGGGCACACAGC[A/G]GGTGCACCATAAACA | 7805 |
| rs566961116 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737889 | CCATCCCACTGACGG[A/G]CAAACCAAGAAAAGC | 7805 |
| rs566974745 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747403 | AACTGTCGCAGGGTC[-/A]AAAATCAGCTCTGTC | 7805 |
| rs566974989 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741521 | TGAAGATCTCCAGAA[C/T]GCAGGTGGGACCGCC | 7805 |
| rs566980978 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750640 | GGATGGCAGAGCTGA[-/C]CCCCTCCCCCATCCC | 7805 |
| rs567135176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736506 | TGGCATGATTATGGC[C/T]CACTGCAGCCTCAAC | 7805 |
| rs567353248 | snp | A/G | 8.51419e-05 | 0.00652409 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739794 | TCCGGTGAGAGGTGG[A/G]GGCTGGGTACTCACA | 7805 |
| rs567418398 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733669 | TGAGCAGCTCACAGG[C/T]CCTGCAGGAGGAGCA | 7805 |
| rs567498489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757202 | GCCCAGGCTCCCTCC[A/G]GGCCCCAGGGGAAGA | 7805 |
| rs567498524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750463 | ACGATGTGGAACCTG[A/C]GGATAGGGAGGGCCG | 7805 |
| rs567517510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740892 | CGCCCCACTCCTCCG[A/G]CCCTGCAAGGGCCAG | 7805 |
| rs567581564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756582 | AGCCAGGATTTGCAT[A/G]CAGGAGTCTGCATCC | 7805 |
| rs567656729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746554 | TGTGACCTTGGGACC[C/T]GAGCCATCCCATGAC | 7805 |
| rs567738027 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745987 | GGGTCAGGGCTCCCC[A/C]CAAGGTTGAACTTGC | 7805 |
| rs567749480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751984 | TCACAAATCACTGCC[C/T]CCAAAGTGGAGCAGA | 7805 |
| rs567755300 | in-del | -/CT | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746938 | CTGGGCATTCACTGA[-/CT]CTCAGTAAACACTCT | 7805 |
| rs567832014 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751293 | CACCCCTCCGTGAAG[C/T]GCACAGAGCTGCAGT | 7805 |
| rs567933898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741450 | TGTTACCAGGGAACT[A/G]AGGTCACCTGCCCAG | 7805 |
| rs567958639 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749333 | AGAAGTCAGTGGGGG[C/T]GGGGCAGTGGCGAGG | 7805 |
| rs568007034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747705 | GGGGCTGGAGGATGG[A/T]AATCAGGGAAGATGG | 7805 |
| rs568019266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748164 | TTATAGAGAAAGGAC[A/C]CAGCCGTCAGTGAGC | 7805 |
| rs568112260 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753778 | TTTAATAACAGCCCA[C/T]GAATATTCATTCACC | 7805 |
| rs568152899 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751696 | GTGAGCCAGGATCAC[A/G]CCACTGCACTCCAGC | 7805 |
| rs568163584 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758355 | ACTGAGGCACAGAGA[A/G]GGGGAATGATTCGTG | 7805 |
| rs568224630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736761 | TTTTAAATTTCTACT[A/G]TGACCTATGTTACTT | 7805 |
| rs568265227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742066 | TGTGGCTGGAGCAAG[A/G]TGTGGGGTGGAGAAT | 7805 |
| rs568349882 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734561 | TCTGTGAGCTAGTAA[A/G]TTCCTGAAGTCAGAT | 7805 |
| rs568375383 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737380 | AATTAGACATCTGAA[C/T]GCAGGTGGCCTTTAC | 7805 |
| rs568695524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748725 | TGGCTGCCTGCAGCT[A/C]CCCAGAGCCTGGCTT | 7805 |
| rs568699764 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754049 | ACTGTTGAAATCATA[C/G]CAGGTGTTAAGTTTT | 7805 |
| rs569002943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747590 | AACACAGCTTCCCCA[A/G]GCTGGCCAGTTGGGG | 7805 |
| rs569063068 | snp | A/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759137 | TGCAAGCTTTGGGCT[A/C]CTGGGAGGCCTGGCC | 7805 |
| rs569064660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746907 | AAGCACAATTGGGTG[A/G]TGGTTTTTGCTACCT | 7805 |
| rs569140065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751838 | AGGGTCTCCTCCAAA[C/T]GATCACTTTTGAGGC | 7805 |
| rs569232144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737330 | GGGCTTGGATTCAAA[C/T]GCAGGCCAGTCCAAA | 7805 |
| rs569318896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757521 | GCCCAGAGCAGGACA[A/G]GGATTTGCCCAGGGT | 7805 |
| rs569419145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736596 | ACGCCACCACATCCA[A/G]CTTTTTTTTTTTTAT | 7805 |
| rs569589935 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759159 | GGCCTGGCCTATCCC[C/T]TCCCAACTTCATTTT | 7805 |
| rs569602866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737887 | CCCCATCCCACTGAC[A/G]GGCAAACCAAGAAAA | 7805 |
| rs569630883 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738172 | ACACATTCTTTGAGA[C/T]GCCTCCCTTCTAAAG | 7805 |
| rs569837980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743512 | GCCATGCAGCCTCTA[A/C]TTAAGTGCTTCCAGC | 7805 |
| rs570086094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748334 | ATGCAGTTTGCCATA[C/T]GGGTCCCAAGTGCCA | 7805 |
| rs570236882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739457 | AACTTGGTTCCAAAG[A/T]AGAAATAATACTGGG | 7805 |
| rs570261150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749866 | TGAATACGCAGCAGG[C/T]CTCAGTAAATGGCAG | 7805 |
| rs570325013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749516 | AAAAATCAAATAGAG[A/G]TTGGCTGGCACCTCC | 7805 |
| rs570337442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744546 | CAAAGTCTCAAGATT[C/T]CAGGATTATCTGAGA | 7805 |
| rs570639698 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740099 | ACTCTGGGGACAGGG[A/G]GTGGATAAGACCCAG | 7805 |
| rs570660561 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737416 | CACATGCCCTAAATG[G/T]GCTGTCTCGGAGGAT | 7805 |
| rs570794562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753650 | GAAACCATCATACCA[A/T]GAGGAACCTAAGGAA | 7805 |
| rs571068840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754655 | TGGGTTCCCAAAGTG[C/T]GCAAGTTTGGGTGAC | 7805 |
| rs571135263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749219 | AGCTCCCAAACATAA[C/T]GTTGGGAGAAAGAAG | 7805 |
| rs571174890 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733532 | GCTTGACAAACTCAC[C/T]AACTTTAGAATGGCC | 7805 |
| rs571277878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745823 | TGCTCAGACCTGCAC[A/G]CACAGGCTTGCACTG | 7805 |
| rs571413903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739433 | AATCATCCTTCTCTT[C/T]CTTTCTTCAACTTGG | 7805 |
| rs571455813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756038 | CAACATCACCTTACC[C/T]CTGACTTTATAAAAG | 7805 |
| rs571498255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751507 | ACTTTGGGAGGCTGA[A/G]GCTGGTGGATCACTT | 7805 |
| rs571561981 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753470 | ACCTTTTCTTAGTAC[A/G]ATGTTCTGAGACTGG | 7805 |
| rs571590567 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740447 | CATACAATTGGACCT[C/T]CCTCCACCAGCCACT | 7805 |
| rs571649969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756409 | ACCTGTGCGTCAGGC[A/G]TGGTTCTGCATGCTT | 7805 |
| rs571652899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740807 | TCCAAGACAGAGTGA[A/G]TGTTAGCAAGGGGAG | 7805 |
| rs571708777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735064 | TTTCTTCTGTTCCAA[A/C]CCTCATCTTACAAAT | 7805 |
| rs571852619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744013 | TGGAAAATTGCAATC[A/G]CTGGATTTAGTGAAG | 7805 |
| rs571954062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734550 | GGCTGCTAAGTTCTG[C/T]GAGCTAGTAAATTCC | 7805 |
| rs572099767 | snp | C/T | 0.000286072 | 0.0119564 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737562 | TGGGCCCAGCACAGC[C/T]TCACCACCCCTCCCA | 7805 |
| rs572294555 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736765 | AAATTTCTACTATGA[C/T]CTATGTTACTTTTAT | 7805 |
| rs572408203 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738471 | GCCCTCAGTTGTCCA[C/G]AGCCCCAGGTACCAT | 7805 |
| rs572431943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739124 | AGTCCCAGTTACTGA[A/G]CGGCACATAGTAGGC | 7805 |
| rs572653556 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733028 | TTCAGCAGAACAATT[C/G]TGTGTTTGAAGGGAC | 7805 |
| rs572691171 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751980 | TCAATCACAAATCAC[C/T]GCCCCCAAAGTGGAG | 7805 |
| rs572855382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755422 | AAAACCTTTATCACC[G/T]CCTCCCCAAACTCCA | 7805 |
| rs573126558 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750498 | ACCATACACTCTCTC[A/G]TGTCAACCTCGCGCC | 7805 |
| rs573132949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746710 | AAGAGCTCGGGTGCT[A/G]GGGTCAGATGGCCCC | 7805 |
| rs573171310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745599 | TTGCCGGATGGCTCA[C/T]GAGACTCATAGAGGG | 7805 |
| rs573249830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734773 | ATTGACCCTCCAAGA[C/G]CAGTTAACTGTCACC | 7805 |
| rs573418465 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757406 | TCGGAGTGAACGTCA[G/T]TTACATTTGCCTGGA | 7805 |
| rs573483338 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750897 | TCCCAAGCAGCCCCT[A/G]TGCAGGGCTGAGGCA | 7805 |
| rs573489966 | in-del | -/A | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749112 | ATGTTATTTTGCAGG[-/A]AAAACAGGCAAATGC | 7805 |
| rs573767490 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732863 | CGCCTATGACTGAAT[C/G]GACTGAATGGATGGC | 7805 |
| rs573805798 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750194 | GGGGGCTCAGAGTTG[A/G]CCTCCAGGTATGACA | 7805 |
| rs573871544 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756994 | AGGAGGAACCAGTGA[C/G]AGCCGTGACTTCACA | 7805 |
| rs573893220 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744937 | AACAGCTACTAAAAA[A/G]TTTCCAGAAATTAAA | 7805 |
| rs573933392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750531 | TCTTGAGAGACAGGT[C/T]CTAACATGAGTCCCA | 7805 |
| rs573938672 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756149 | TGCTACCTGTGAGGC[A/G]CCCCTGCATGCCACA | 7805 |
| rs574002065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750026 | CGGCTCAGATGGCGC[C/T]GGAGGAGGTTGTCAC | 7805 |
| rs574082726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740470 | CAGCCACTCCCAGGG[A/G]TCCAAAGTCACAGTA | 7805 |
| rs574211635 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744156 | AGGAGCACGGTGCAT[C/G]CTCTAACTGCCCCCT | 7805 |
| rs574405174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746971 | TGAGCACCTACCGCC[C/T]CCAAACTCTGTCTAG | 7805 |
| rs574417972 | in-del | -/CACA | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738156 | ATTTGCAAATATTAC[-/CACA]CATTCTTTGAGACGC | 7805 |
| rs574467527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746675 | GTCCCTTCATTCTAT[A/G]CTGGTGAGATCATGA | 7805 |
| rs574751309 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758584 | CTGTGCGCCAGGCCC[C/T]GGGCTAGGCTTCTCT | 7805 |
| rs574774147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735415 | CATTCTGGTTGGGGG[C/T]TCCTCACCAGCCAGT | 7805 |
| rs574782767 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740431 | TCCCCACCACGCCCC[A/G]CATACAATTGGACCT | 7805 |
| rs574784700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736151 | CTTCCCCCATGAGGC[C/T]TTCAGGGGTGTTCTC | 7805 |
| rs574793418 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759226 | GCCTGACATCATAGA[A/G]AGGTGACACAGTGCA | 7805 |
| rs574952752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756817 | CCCCAGGAGGAAGTC[A/G]CTTGGGTCTAGGGGA | 7805 |
| rs575007559 | snp | A/G | 0.000108249 | 0.00735612 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742600 | GCATCACGGCCCCCC[A/G]ACCAGCCCCTCCCAC | 7805 |
| rs575049144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742180 | CCACTGACGGCTTTA[A/C]GCAGAAGAGTGAGGC | 7805 |
| rs575135797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752932 | CTGCCTCAGCCTCCC[A/G]CGTAGCTTGGACTAC | 7805 |
| rs575166768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746150 | TGTGGCCCTGGCCAG[A/G]TTCTGGCTTCTCCCT | 7805 |
| rs575225247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748388 | TCAGGGCTGCTCCAC[C/G]CTGACCCTGTGTCCT | 7805 |
| rs575318890 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752774 | CTGCACGAGGTCAGG[A/G]CAATAGAGACTCCTT | 7805 |
| rs575482265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735406 | CGGACCTCTCATTCT[C/G]GTTGGGGGTTCCTCA | 7805 |
| rs575492907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746647 | CCCCAATTACAGCAT[C/T]TTTTCACCCACTGTC | 7805 |
| rs575605013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737439 | CGGAGGATCCCAAGT[A/C]AAGTCAGAGGAGCTG | 7805 |
| rs575721330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738682 | GCCAAAGCCCTCTCT[A/G]GGATCATGCAGGGCT | 7805 |
| rs575730628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742159 | TTATTCTAGTGTGAT[A/G]AGCAGCCACTGACGG | 7805 |
| rs575750460 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757804 | CTGGTGCCTGGAGCA[A/G]GGCAGAGAAGGGGAA | 7805 |
| rs575828941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747843 | GTGACCATGTGAGGC[A/G]GGGAGTGGCTGTTGG | 7805 |
| rs575914376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752365 | AAAAGCAAAGGACTC[A/G]GGCAGGTCCCACCCC | 7805 |
| rs576067510 | snp | A/G | 1.84964e-05 | 0.00304103 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742552 | AGACGCTCATGATCT[A/G]GAGGCAAAGCAAAGC | 7805 |
| rs576388664 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752099 | AGAAATGAATGGTGG[A/G]AGGCTGGATGAGGGC | 7805 |
| rs576402247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742109 | CTGTCAGAGAGGTGG[A/G]CAGAGGCTGGATCCT | 7805 |
| rs576497511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748791 | CACCCGCCGCCTCCA[C/T]CTCATCCCCTCCTCC | 7805 |
| rs576674055 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732198 | GCGTGTGTGGAGGGG[C/T]GTGGGGGGTGTGAGT | 7805 |
| rs576810725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738882 | CACAGAGACGTGAAG[C/T]AACCTGTTCAAGGCC | 7805 |
| rs577017654 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735855 | CCCCCTGAGTAAGAG[A/G]AGAGGGTCCTGTACT | 7805 |
| rs577051122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736854 | GCTTCAGGCCACAGG[A/C]CCCCATTGTGGCCTC | 7805 |
| rs577291113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753141 | CAAAGTAAAGTACCA[C/T]TGGATTATAACCCAA | 7805 |
| rs577347799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748553 | ACCATCAAGAGGAAG[C/T]TCCCCTTCCCCACCC | 7805 |
| rs577451591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744125 | GGGCAAGCTTACGTG[A/G]TTCGGCAGTAGTACC | 7805 |
| rs577619649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743073 | AGGCCCAGGAGGGCC[C/T]TGGAGAGCATCTAAC | 7805 |
| rs577708112 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732086 | GATCAGACAGCATTG[G/T]GTCAGGACCACCCCT | 7805 |
| rs577880671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745331 | ATTCCCTCCGCTGCC[C/T]GGCATCTTCCAGCCA | 7805 |
| rs577942657 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733178 | CGCCAGAGTTGGCAT[A/C]CAGTTGATGGGTTCA | 7805 |
| rs745573395 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756825 | GGAAGTCGCTTGGGT[C/G]TAGGGGAGATGAGTG | 7805 |
| rs745667466 | snp | C/T | 2.04171e-05 | 0.00319502 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757637 | GCACGCACGCACACA[C/T]ACCCGGGGCCCGCAC | 7805 |
| rs745856514 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733574 | CAAGTGTCAGAGCTG[A/G]TTGAAATAAACCAAG | 7805 |
| rs745863820 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741802 | ACTTGGGGAACCACT[G/T]GTTTGGGGACATGAG | 7805 |
| rs745872473 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750993 | TGGGGTCCCCTGGGA[A/G]ACCAACGCTCGCCTC | 7805 |
| rs745951239 | snp | A/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757844 | TGCCCTCCTCACTTC[A/C]TTCCTGCCCCTTAGA | 7805 |
| rs745956158 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746030 | CCAGGATCTCTCTAG[C/T]CATCTGCCCACCCTT | 7805 |
| rs746019936 | snp | A/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759543 | AAACACACTGACAGC[A/C]TGTGGAATAATTGTA | 7805 |
| rs746140587 | snp | A/G | 1.65072e-05 | 0.00287286 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735143 | AGGGAGTTAGTGACA[A/G]GGCTGGCACCCACCT | 7805 |
| rs746167830 | in-del | -/G | 7.18881e-05 | 0.00599491 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742437 | CCCCGCCACTCCACC[-/G]GGCGTCCCCTGGACC | 7805 |
| rs746191196 | snp | C/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740747 | CTGCACAAGCACCCA[C/G]AGCCACCCTGCACAA | 7805 |
| rs746220804 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739275 | AGGTCTCCAGACTCC[C/T]GGGCCAGGGCCCTTC | 7805 |
| rs746263342 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30735229 | TCATGCACTTGATCA[A/G]TCTGTAGCACCGCCA | 7805 |
| rs746437333 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753422 | GCCGGGGGCTCAAAG[C/T]CACCAGCAACAGTGG | 7805 |
| rs746510319 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748858 | AACCCCAGTGCAGCC[A/G]CTGATCCCCTGTGGG | 7805 |
| rs746538562 | snp | C/T | 2.05341e-05 | 0.00320416 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733800 | CAGCTCCACCCCTCC[C/T]AGCACTGGGGCTGGG | 7805 |
| rs746538740 | snp | C/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733791 | ATTATGAGGCAGCTC[C/T]ACCCCTCCCAGCACT | 7805 |
| rs746540217 | snp | C/T | 2.57968e-05 | 0.00359134 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741690 | TGAAGAGCATGGTGA[C/T]GAGCAGGAAGCTGGA | 7805 |
| rs746591610 | snp | C/G | 1.71767e-05 | 0.00293054 | missense | LAPTM5 | GRCh38.p7 | 1:30733868 | GCTGGGCCCCCCTCT[C/G]GGGTCTTCGATGGCA | 7805 |
| rs746705065 | snp | C/T | 1.68912e-05 | 0.00290608 | missense | LAPTM5 | GRCh38.p7 | 1:30757699 | GTTGCGATGCGGACA[C/T]TGAAGCAGCAGCAGG | 7805 |
| rs746771600 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752172 | GAAGGAACTCATTTG[C/T]CCACTTTCTGGATCA | 7805 |
| rs746801722 | snp | A/C | 3.47457e-05 | 0.00416793 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738928 | GGGCATGGTTCCCTG[A/C]CCCAGACTCACCATG | 7805 |
| rs746831429 | snp | C/G | 7.0619e-05 | 0.00594176 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757765 | CTGCCGTCCCCTCCT[C/G]TGAGACACTGAAGGG | 7805 |
| rs746983240 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30731982 | TTGAGGTCTTCCCCA[A/G]TGTCCAGAGCAGGAC | 7805 |
| rs747061899 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755924 | GGTGGGCCAAGCAAG[A/G]GCTCCCGGGGTCACC | 7805 |
| rs747062918 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747667 | AGGAGCAAGCAACAG[G/T]TTGAGCTAAAAGAAT | 7805 |
| rs747071350 | snp | A/G | 1.78592e-05 | 0.00298819 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742541 | GATGAACAACAAGAC[A/G]CTCATGATCTGGAGG | 7805 |
| rs747250644 | snp | C/T | 2.14286e-05 | 0.0032732 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757625 | ACACTCACACAAGCA[C/T]GCACGCACACACACC | 7805 |
| rs747349412 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742719 | GCCTTTACACACAGA[A/G]AGCCCATGTTCAGAA | 7805 |
| rs747515424 | snp | A/G | 3.38375e-05 | 0.0041131 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739911 | GATTTGCAGGGACAG[A/G]AAGGGCAGCAGGTAC | 7805 |
| rs747607677 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746866 | GTGGTGCGCGGAGCC[G/T]GGCACACAGCAGGTG | 7805 |
| rs747685590 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749343 | GGGGGCGGGGCAGTG[A/G]CGAGGCGGGGGCTCT | 7805 |
| rs747707641 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749667 | GAGCTCAGGGTCCAA[A/C]CGTAGGGGTCAGGGC | 7805 |
| rs747720009 | snp | C/T | 5.5746e-05 | 0.0052792 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733949 | GATGAGGGCTGAGTA[C/T]GGTCAAGAATGACCT | 7805 |
| rs747821156 | snp | C/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740781 | AAACGGCCTCCCCAG[C/G]CAGCATGGGTTCCAA | 7805 |
| rs747836782 | snp | C/G | 2.53155e-05 | 0.00355768 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739148 | AGTAGGCCCTCACTT[C/G]AGAGACCGTCTCAGC | 7805 |
| rs747902976 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745487 | GTATTTCTACTTTTG[C/T]GAAAACCACCTGCAT | 7805 |
| rs747913395 | in-del | -/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746584 | CAGGTACAAGGCTTC[-/T]CTCCCCCAACAATGC | 7805 |
| rs747955844 | snp | A/G | 1.68664e-05 | 0.00290395 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739814 | GGGTACTCACAGCAC[A/G]GCTCCGGGAGGCCAA | 7805 |
| rs747961072 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744302 | GAGAGAAAAAAACTC[A/C]TTCCTCAGCCCCTAA | 7805 |
| rs748101324 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749039 | TGTGGACACCCAGCA[C/T]GGAGCCTGGTGGCCA | 7805 |
| rs748138740 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734744 | CCTTCTGCTTTCCCA[G/T]CTATCTCATATCCAT | 7805 |
| rs748243923 | in-del | -/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732001 | CCAGAGCAGGACCCA[-/G]CCCCAGGGGAGTGGA | 7805 |
| rs748257104 | snp | A/G/T | 8.36415e-05 | 0.00646645 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737583 | ACCCCTCCCAGAGCC[A/G/T]CAGGGCAGGGATCCA | 7805 |
| rs748500779 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747935 | GTGACAGTGATGGGG[A/G]TGACGGCAATGGGGA | 7805 |
| rs748547372 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755534 | ACAACCAAACTCTCC[C/T]TCCTGCCAATGGCAC | 7805 |
| rs748558406 | snp | C/G | 4.19032e-05 | 0.0045771 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741635 | CGGGGCTCCTGAGCC[C/G]TCACCTTGACTACGC | 7805 |
| rs748594187 | snp | A/G | 3.33172e-05 | 0.00408136 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741738 | GGCAAGGAGAGCAGG[A/G]AGGTGCTCAGGGGTG | 7805 |
| rs748747039 | snp | A/C | | | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741694 | GAGCATGGTGATGAG[A/C]AGGAAGCTGGAGATC | 7805 |
| rs748754711 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737119 | TGGACCCTATCCTCT[A/G]GGCCTGACCACCCCA | 7805 |
| rs748884714 | snp | A/C | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754564 | CAAAACAAAACAAAT[A/C]AAACCACAAAAGATG | 7805 |
| rs748945466 | snp | A/G | 1.6713e-05 | 0.00289072 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739874 | AGCCCAGCAGGGTGA[A/G]CAGGCACAGGAGATA | 7805 |
| rs749000897 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735682 | AGCAGATTACAAAAC[A/C]GCATGTGCAGTATTG | 7805 |
| rs749275573 | snp | A/G | 4.25541e-05 | 0.00461251 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757630 | CACACAAGCACGCAC[A/G]CACACACACCCGGGG | 7805 |
| rs749305657 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744392 | AGGCAGATGACAGCT[C/G]CGTCCAGCACAGAAC | 7805 |
| rs749337967 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740818 | GTGAGTGTTAGCAAG[A/G]GGAGTGGGTGCTGGC | 7805 |
| rs749427424 | in-del | -/C | 2.8475e-05 | 0.00377316 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742409 | CCTGGCCAGGGCCCT[-/C]CCTGTCCTCCTCCCC | 7805 |
| rs749593940 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745649 | CACAGAGCGAGGCAA[C/T]CTCAGAGCCTGACTT | 7805 |
| rs749676076 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748783 | CTCGTCCTCACCCGC[C/T]GCCTCCACCTCATCC | 7805 |
| rs749689314 | snp | A/G | 5.16676e-05 | 0.00508243 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733900 | AGACAGGGCTTCCTC[A/G]TAGGACGGCAGGACC | 7805 |
| rs749694580 | snp | C/T | 1.99762e-05 | 0.00316033 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733962 | TATGGTCAAGAATGA[C/T]CTGCAATTCCAACCT | 7805 |
| rs749943141 | in-del | -/GGGAGGGGC | 0.00015727 | 0.00886624 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733720 | CAGATTGTCCTGCCA[-/GGGAGGGGC]GGGAGGGGCGGGAGG | 7805 |
| rs749953789 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752064 | GAGGAGGAAGCTTCC[C/T]GTAAACTGGACCATA | 7805 |
| rs750073164 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734474 | TAGAGTCAAGAGTTG[A/G]AGAGGACGAGATCAT | 7805 |
| rs750114612 | snp | C/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733722 | AGATTGTCCTGCCAG[C/G]GAGGGGCGGGAGGGC | 7805 |
| rs750126151 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745028 | CCTTGGACATTACCC[A/G]ACTTTAGAGACCTCT | 7805 |
| rs750160139 | snp | A/G | 0.000107837 | 0.00734213 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741670 | CAGTAGGCTCAGGCT[A/G]ATGATGAAGAGCATG | 7805 |
| rs750201690 | snp | A/G | 1.74512e-05 | 0.00295386 | missense | LAPTM5 | GRCh38.p7 | 1:30733847 | ACCTCTGAGTATGGG[A/G]GTGGTGCTGGGCCCC | 7805 |
| rs750269795 | snp | A/G | 1.76157e-05 | 0.00296775 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733921 | CGGCAGGACCACCTG[A/G]GAGAGACAGAGAGAT | 7805 |
| rs750272905 | snp | C/T | 0.000700307 | 0.0186993 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742426 | CTGTCCTCCTCCCCC[C/T]GCCACTCCACCGGCG | 7805 |
| rs750377752 | snp | C/G | 3.48056e-05 | 0.00417152 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757754 | GGTCCATGGTGCTGC[C/G]GTCCCCTCCTCTGAG | 7805 |
| rs750430417 | in-del | -/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755504 | ACCTGTTTCTCCTCA[-/C]CTTCCATACTGCCCA | 7805 |
| rs750488840 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755175 | GTCTCATCACTCATA[A/G]GCATTGGTTCTCAAC | 7805 |
| rs750546368 | snp | C/T | 1.67231e-05 | 0.00289159 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739853 | AGGCGGGCAGCTCAA[C/T]GTAGGAGCCCAGCAG | 7805 |
| rs750675040 | snp | G/T | 3.40617e-05 | 0.0041267 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733662 | CCAGTTGTGAGCAGC[G/T]CACAGGCCCTGCAGG | 7805 |
| rs750701613 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750131 | CCAGCAGCAGAGATA[C/T]TCTGGCTGGTGGTAG | 7805 |
| rs750706620 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747496 | CCACTCTCCTTTCCC[G/T]CTTTTCACCTCTTCT | 7805 |
| rs750773128 | snp | C/T | 2.19652e-05 | 0.00331393 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757614 | CGCAGACATTCACAC[C/T]CACACAAGCACGCAC | 7805 |
| rs750987530 | snp | A/C | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732683 | GCTGTTGGGGCCAAA[A/C]CTCCCCAGCTGCCAC | 7805 |
| rs751068509 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755244 | TTATCACAAGTGGCA[G/T]GGTAGGGAGATGGGC | 7805 |
| rs751072665 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746605 | CCAACAATGCGCAGG[C/T]AGACAGCATGCCCTC | 7805 |
| rs751119579 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753819 | AACGCACCACACTAA[C/T]GTTGAGACGTTAGCA | 7805 |
| rs751127426 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745325 | TGGCCAATTCCCTCC[A/G]CTGCCCGGCATCTTC | 7805 |
| rs751189204 | snp | A/C | 9.98752e-05 | 0.00706595 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742430 | CCTCCTCCCCCCGCC[A/C]CTCCACCGGCGTCCC | 7805 |
| rs751230201 | in-del | -/C | 4.99332e-05 | 0.00499641 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742593 | GAGCCTGCATCACGG[-/C]CCCCCCGACCAGCCC | 7805 |
| rs751273668 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735380 | GAAGCCAGCATCCAG[A/C]TGCTCCTGCTCGGAC | 7805 |
| rs751279906 | snp | A/G | 1.72389e-05 | 0.00293584 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742506 | GACGCCTTGCCATGG[A/G]CCACCTCTACTGAGT | 7805 |
| rs751283633 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759071 | CCACAAAACTTGATT[A/G]GTGGACTTGATCAAT | 7805 |
| rs751303305 | snp | A/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735524 | ACCCTCCAATTTCCC[A/T]GGCAATAGTCCCACA | 7805 |
| rs751311751 | snp | A/G | 1.78637e-05 | 0.00298857 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733930 | CACCTGGGAGAGACA[A/G]AGAGATGAGGGCTGA | 7805 |
| rs751354799 | in-del | -/CTC | 6.59065e-05 | 0.00574012 | cds-indel | LAPTM5 | GRCh38.p7 | 1:30735200 | CTTGGAGTTTCTCTT[-/CTC]CTCCACCGAGTTCAT | 7805 |
| rs751366621 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | LAPTM5 | GRCh38.p7 | 1:30735184 | TCACCTTCTGGAGCA[C/T]CTTGGAGTTTCTCTT | 7805 |
| rs751499012 | snp | G/T | 1.70136e-05 | 0.00291659 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739796 | CGGTGAGAGGTGGGG[G/T]CTGGGTACTCACAGC | 7805 |
| rs751606649 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752869 | TAGAGCGCAGTGGCG[A/C]GATCTCGGCTCACTG | 7805 |
| rs751735631 | snp | A/G | 1.83263e-05 | 0.00302701 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733824 | GGCTGGGGCCTGGCG[A/G]GGGTCACACCTCTGA | 7805 |
| rs751766368 | snp | C/T | | | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738664 | CTGTGTTGCAATTCA[C/T]ATGCCAAAGCCCTCT | 7805 |
| rs751830962 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742279 | GGGTGGGGTCAGGTG[A/G]AACATCCCCATTTGC | 7805 |
| rs751925799 | snp | G/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750781 | CTCATCTGTAAAATG[G/T]AGGCCCCCGTGGCAG | 7805 |
| rs752042414 | snp | C/T | 6.61485e-05 | 0.00575064 | synonymous-codon, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739036 | GTCCAGCAGCTGCAG[C/T]GTCATCAGGGGGAAC | 7805 |
| rs752103634 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733358 | TATTTATATATAGGG[A/G]GTAACTAATTAATGA | 7805 |
| rs752110174 | snp | C/T | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743686 | CTATCTCTATTAATA[C/T]GGCCCTAAGTTTACA | 7805 |
| rs752182650 | snp | A/G | 3.43666e-05 | 0.00414513 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742518 | TGGGCCACCTCTACT[A/G]AGTGCTCGATGAACA | 7805 |
| rs752412840 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750254 | TATCTGGGGAAGCAC[C/T]CTCCACTCCCCAAAC | 7805 |
| rs752448690 | snp | G/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752956 | GGACTACAGGCTCCC[G/T]CCATCATGCCCAGCT | 7805 |
| rs752463551 | snp | A/G | 1.64931e-05 | 0.00287163 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735290 | GGCCCAGGTCAGGCT[A/G]TGCTTTGCTGAGCGT | 7805 |
| rs752561925 | snp | A/G | 1.67147e-05 | 0.00289086 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739859 | GCAGCTCAATGTAGG[A/G]GCCCAGCAGGGTGAG | 7805 |
| rs752565312 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747142 | TTAGGGAGAATTTCA[C/T]CAACAGGAAACCCAT | 7805 |
| rs752676339 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741915 | TAGCACAGGAGGATG[C/T]GACAGAGGGTGCTGG | 7805 |
| rs752698551 | in-del | -/G | 0.000114587 | 0.00756838 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741612 | TAACAGGAAGGGGCA[-/G]GGGGCAGCGGGGCTC | 7805 |
| rs752782257 | snp | A/C | 5.33248e-05 | 0.00516329 | missense, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738977 | TTGAGATAGGTGGGC[A/C]CTTCCATGTAGGAGC | 7805 |
| rs752828139 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758754 | AGCCACAACTCTTAG[A/G]CAAGCTACCCTGGAA | 7805 |
| rs752914718 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740150 | TGGTGTCCCAGGAGA[C/T]GTAAGGGAACCATCC | 7805 |
| rs752997168 | snp | C/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733563 | AATCGTCTAAACAAG[C/T]GTCAGAGCTGATTGA | 7805 |
| rs753079584 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756749 | ATCTAGGCTAATTTT[C/G]AGGAAGCCCTTCCAG | 7805 |
| rs753228367 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734359 | CTTCTTTTTCTGTTG[A/G]GATTTCTGAGAGGGT | 7805 |
| rs753245704 | snp | C/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750869 | AAATTGAGGCTGGGG[C/G]ACGGGTGCCTTGTCC | 7805 |
| rs753293212 | snp | A/G | 0.000141466 | 0.0084091 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742438 | CCCCGCCACTCCACC[A/G]GCGTCCCCTGGACCT | 7805 |
| rs753478282 | snp | A/G | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743752 | GCTCAGCTGACAGGC[A/G]ACCAGCCACCCACCA | 7805 |
| rs753574128 | snp | G/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751864 | GAGGCAGGGACCACT[G/T]GCCCCATTTACAGAT | 7805 |
| rs753591777 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746814 | GGGGATAATCACTGA[C/T]CTGCCTCACAGGATT | 7805 |
| rs753632054 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755038 | AGAGAGGACTCTTTC[A/G]GGGTGCAGGAAGATA | 7805 |
| rs753633367 | snp | A/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747212 | AGAAGAGAAGAAAGC[A/T]TTCCAAAAGAGCAGA | 7805 |
| rs753702211 | snp | G/T | 6.35708e-05 | 0.00563749 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741591 | CCCACCACCAGTGGG[G/T]GTGAATAACAGGAAG | 7805 |
| rs753772587 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748424 | CTCACACTTCTGCCA[C/T]CATCATTATTATTAT | 7805 |
| rs753823055 | snp | G/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759086 | GGTGGACTTGATCAA[G/T]CCATTCTCCATGTGC | 7805 |
| rs753841515 | snp | C/G/T | 8.77795e-05 | 0.00662446 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733843 | TCACACCTCTGAGTA[C/G/T]GGGGGTGGTGCTGGG | 7805 |
| rs753862296 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738070 | GAGGTTACATTCCCT[C/T]CCCTAGGGGCAGCTT | 7805 |
| rs753866362 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736536 | CCTCCCAGGCTCAAG[C/T]GATCCTCCCGCTTCA | 7805 |
| rs753976433 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750062 | GCACAGGAAGTGCTG[C/T]GACTGGGCGCTAGCA | 7805 |
| rs754054231 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744557 | GATTCCAGGATTATC[G/T]GAGATCTGGAACAAA | 7805 |
| rs754076563 | snp | A/G | 1.67447e-05 | 0.00289345 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739844 | ACTTGAGGTAGGCGG[A/G]CAGCTCAATGTAGGA | 7805 |
| rs754280208 | snp | A/G | 5.1971e-05 | 0.00509733 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742526 | CTCTACTGAGTGCTC[A/G]ATGAACAACAAGACG | 7805 |
| rs754385997 | snp | A/C | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740639 | TCGTCTAAAATCACT[A/C]AGGAGGCAACCAGAA | 7805 |
| rs754429654 | snp | C/T | 3.29527e-05 | 0.00405898 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30735209 | TCTCTTCTCCTCCAC[C/T]GAGTTCATGCACTTG | 7805 |
| rs754504521 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735450 | AATATTCCAGGTATT[G/T]CCCTTTTCATTGCCC | 7805 |
| rs754537548 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734671 | ACCAGGAATTTAAAC[C/T]GTCACTTTCCAATAA | 7805 |
| rs754544676 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749722 | TGAAGAAGATTCCCC[A/G]AAAGAGCAATGGAAA | 7805 |
| rs754580360 | snp | C/T | 4.94132e-05 | 0.00497033 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742432 | TCCTCCCCCCGCCAC[C/T]CCACCGGCGTCCCCT | 7805 |
| rs754632215 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759081 | TGATTGGTGGACTTG[A/G]TCAATCCATTCTCCA | 7805 |
| rs754777044 | in-del | -/ATCA | 1.69072e-05 | 0.00290746 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737721 | AGATTTGGGGGCCAC[-/ATCA]ATCAATGTCTCTGGA | 7805 |
| rs754807949 | in-del | -/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757389 | CAGAAACGGAGCCAG[-/C]CTCGGAGTGAACGTC | 7805 |
| rs754872054 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752228 | GGGACCTGAAGCAAG[C/G]TCCTGCCCCATCTCT | 7805 |
| rs754879200 | snp | C/G | 1.6974e-05 | 0.0029132 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739801 | AGAGGTGGGGGCTGG[C/G]TACTCACAGCACGGC | 7805 |
| rs755015211 | snp | C/G | 2.24374e-05 | 0.00334936 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733695 | GAGCAGGCCAGCGAG[C/G]GAGACACAAGCAGAT | 7805 |
| rs755082105 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749218 | AAGCTCCCAAACATA[A/G]CGTTGGGAGAAAGAA | 7805 |
| rs755095880 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744589 | CCTAGAATCAGATCA[C/T]CTCAACCTCCCCTTG | 7805 |
| rs755149045 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742251 | TCCATCTGCTCTCAC[C/G]ACCTGCAGATGTGGG | 7805 |
| rs755163339 | snp | A/G | 2.15431e-05 | 0.00328194 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757626 | CACTCACACAAGCAC[A/G]CACGCACACACACCC | 7805 |
| rs755172056 | snp | A/C | | | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738763 | AACCTGCCTTCCTCA[A/C]TCCTGACAAGTTTCT | 7805 |
| rs755216643 | snp | C/T | 3.41799e-05 | 0.00413385 | missense | LAPTM5 | GRCh38.p7 | 1:30757679 | GGTAGATGGCCAGGG[C/T]GGTGGTTGCGATGCG | 7805 |
| rs755358657 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742309 | CGGATGAAACAGCTG[A/C]GGCCCCAAGAAAGGA | 7805 |
| rs755548836 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755426 | CCTTTATCACCTCCT[C/T]CCCAAACTCCAGGTT | 7805 |
| rs755574951 | snp | A/G | 1.72356e-05 | 0.00293556 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742522 | CCACCTCTACTGAGT[A/G]CTCGATGAACAACAA | 7805 |
| rs755607701 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750270 | CTCCACTCCCCAAAC[A/G]ATTCCCTAAAACCAT | 7805 |
| rs755659020 | snp | A/G | 3.29527e-05 | 0.00405898 | missense | LAPTM5 | GRCh38.p7 | 1:30735207 | TTTCTCTTCTCCTCC[A/G]CCGAGTTCATGCACT | 7805 |
| rs755855783 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755644 | CATTTACAGGTGAGG[A/G]CATCGGATGGCACGA | 7805 |
| rs755858176 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746696 | GAGATCATGAAGATA[A/C]GAGCTCGGGTGCTGG | 7805 |
| rs755982816 | snp | A/C | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753590 | CAAAATGCCTGACAA[A/C]TACTCCTCGAACTGT | 7805 |
| rs756057209 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736224 | AGAAGATGCTAAAAG[G/T]GGCAAGGTTCTGTTT | 7805 |
| rs756059217 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735604 | CAGCCCTGCCCATCT[C/T]GAAACAGAGCTGATG | 7805 |
| rs756171596 | snp | G/T | | | missense, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738991 | CACTTCCATGTAGGA[G/T]CTGCAGAGGGTCAGG | 7805 |
| rs756191709 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740169 | AGGGAACCATCCCCA[C/T]CTATCAGGGCTCAAA | 7805 |
| rs756218747 | snp | C/G | 1.72606e-05 | 0.00293768 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757746 | CAAGCGGGGGTCCAT[C/G]GTGCTGCCGTCCCCT | 7805 |
| rs756310339 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753211 | AAATCATTTATTTAT[A/G]TAATAAACTGGGAGT | 7805 |
| rs756332410 | snp | A/C | 1.70017e-05 | 0.00291558 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737730 | GGGCCACATCAATGT[A/C]TCTGGACATAAGGAA | 7805 |
| rs756356075 | in-del | -/TTTT/TTTTT | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743795 | TGCTGACTGTGTGGG[-/TTTT/TTTTT]TTTTTTTTTTTTTTT | 7805 |
| rs756385276 | snp | C/T | 1.64999e-05 | 0.00287222 | synonymous-codon, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739051 | CGTCATCAGGGGGAA[C/T]TTGGAGGAGCTCTGG | 7805 |
| rs756505338 | snp | C/T | 0.000169823 | 0.00921317 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733691 | GGAGGAGCAGGCCAG[C/T]GAGGGAGACACAAGC | 7805 |
| rs756534535 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748763 | CTCTTCACTCTTCCG[C/T]AGTTCTCGTCCTCAC | 7805 |
| rs756550018 | snp | A/G/T | 4.65476e-05 | 0.00482411 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742439 | CCCGCCACTCCACCG[A/G/T]CGTCCCCTGGACCTA | 7805 |
| rs756595715 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756805 | GGCCCTGAGTCACCC[A/C]AGGAGGAAGTCGCTT | 7805 |
| rs756812417 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735929 | GGCAAGGAGACATAT[A/G]GAGGTACGGAGTGAC | 7805 |
| rs756863556 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755287 | ATCTAGTAGGTAGAG[A/C]CCATGGATGCTGCTG | 7805 |
| rs757009420 | snp | C/T | 0.000301614 | 0.0122766 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733729 | CCTGCCAGGGAGGGG[C/T]GGGAGGGCCCACCCA | 7805 |
| rs757406014 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746815 | GGGATAATCACTGAC[C/T]TGCCTCACAGGATTG | 7805 |
| rs757413921 | snp | A/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738449 | TTCATCCTTCAGATC[A/T]AATCAAGCCCTCAGT | 7805 |
| rs757432928 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741424 | ACCATGCCCGGCCCC[A/G]TGGAGGCTCATGTTA | 7805 |
| rs757605563 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745126 | CTCCAATCACCCCAG[G/T]GGAAGAAGGGGACAT | 7805 |
| rs757624388 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749668 | AGCTCAGGGTCCAAC[C/T]GTAGGGGTCAGGGCG | 7805 |
| rs757632662 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747664 | CTGAGGAGCAAGCAA[C/G]AGGTTGAGCTAAAAG | 7805 |
| rs757677495 | snp | G/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758990 | GCAGCCCATCATTTC[G/T]GCCCCAGGAGAGGTT | 7805 |
| rs757686195 | snp | A/G | 0.000400498 | 0.0141453 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742529 | TACTGAGTGCTCGAT[A/G]AACAACAAGACGCTC | 7805 |
| rs757838842 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745193 | ACTACCCAGAAAAGG[A/G]ACTATTCTTAATACT | 7805 |
| rs757918780 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733730 | CTGCCAGGGAGGGGC[A/G]GGAGGGCCCACCCAG | 7805 |
| rs757924682 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732464 | AGAAACACATCAGCC[A/G]GACAGAAGCTTGTTG | 7805 |
| rs757926557 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734528 | GGCCCAAGCCAGACC[C/T]ACATTTGGCTGCTAA | 7805 |
| rs757971833 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744101 | GCAAACAGAATCTGC[G/T]TTTGGCTGGGGCAAG | 7805 |
| rs758050735 | snp | A/G | 5.89779e-05 | 0.00543005 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741608 | TGAATAACAGGAAGG[A/G]GCAGGGGGCAGCGGG | 7805 |
| rs758079710 | snp | C/T | 1.73078e-05 | 0.0029417 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733855 | GTATGGGGGTGGTGC[C/T]GGGCCCCCCTCTGGG | 7805 |
| rs758091551 | snp | A/T | 2.6294e-05 | 0.00362578 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741675 | GGCTCAGGCTGATGA[A/T]GAAGAGCATGGTGAT | 7805 |
| rs758096986 | snp | A/G | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732328 | TGGGTGTTTGGGTGT[A/G]TTTGTGGGTGTGTGG | 7805 |
| rs758207717 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737815 | GAGCACAGCGTGGCA[C/T]AGCCGTCACCTTGGT | 7805 |
| rs758325705 | snp | A/G | 1.74303e-05 | 0.00295209 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757755 | GTCCATGGTGCTGCC[A/G]TCCCCTCCTCTGAGA | 7805 |
| rs758365612 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752065 | AGGAGGAAGCTTCCC[A/G]TAAACTGGACCATAA | 7805 |
| rs758422746 | snp | A/T | 1.67206e-05 | 0.00289137 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739856 | CGGGCAGCTCAATGT[A/T]GGAGCCCAGCAGGGT | 7805 |
| rs758457320 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747544 | TCAGTTCTTATTCCC[A/G]TCTGCACGCAGCCTT | 7805 |
| rs758460536 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755181 | TCACTCATAGGCATT[G/T]GTTCTCAACTGGGAG | 7805 |
| rs758503863 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756259 | GCTTCTCTCAGCTCT[C/T]GCATTGGCAGGAGCT | 7805 |
| rs758545350 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736757 | TAGTTTTTAAATTTC[C/T]ACTATGACCTATGTT | 7805 |
| rs758731121 | snp | A/G | 2.16242e-05 | 0.0032881 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757620 | CATTCACACTCACAC[A/G]AGCACGCACGCACAC | 7805 |
| rs758807421 | snp | G/T | 1.6501e-05 | 0.00287232 | missense | LAPTM5 | GRCh38.p7 | 1:30737664 | CATCTTGATGAACTG[G/T]TTATGAGGCATATCC | 7805 |
| rs758917378 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744893 | TTACACGCATGTGTT[A/G]CTGTCCTAGTTTATC | 7805 |
| rs758999171 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754656 | GGGTTCCCAAAGTGT[A/G]CAAGTTTGGGTGACC | 7805 |
| rs759057891 | snp | A/C | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743458 | TGCAGTTTTAAAGAA[A/C]CTTGGAGGTCACCTT | 7805 |
| rs759085137 | snp | C/T | 1.71661e-05 | 0.00292963 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742516 | CATGGGCCACCTCTA[C/T]TGAGTGCTCGATGAA | 7805 |
| rs759087419 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747059 | ATGGTGTGCTCAGAG[C/T]CATGACAGAGGACAC | 7805 |
| rs759314826 | snp | G/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759144 | TTTGGGCTCCTGGGA[G/T]GCCTGGCCTATCCCT | 7805 |
| rs759332423 | snp | C/T | 2.4268e-05 | 0.00348331 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742591 | GCTGAGCCTGCATCA[C/T]GGCCCCCCGACCAGC | 7805 |
| rs759360466 | snp | G/T | 1.64817e-05 | 0.00287064 | missense | LAPTM5 | GRCh38.p7 | 1:30735187 | CCTTCTGGAGCATCT[G/T]GGAGTTTCTCTTCTC | 7805 |
| rs759421669 | snp | G/T | 1.64933e-05 | 0.00287165 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735287 | AAAGGCCCAGGTCAG[G/T]CTGTGCTTTGCTGAG | 7805 |
| rs759460856 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753838 | GAGACGTTAGCAATA[A/G]AGGAACTAGGCATGG | 7805 |
| rs759488183 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735026 | GAATGAATCTTAGAC[C/T]ACCAGAACTGAAAGA | 7805 |
| rs759546359 | snp | A/G | 3.32867e-05 | 0.00407949 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737593 | GAGCCGCAGGGCAGG[A/G]ATCCACTCACCTTGA | 7805 |
| rs759669634 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734305 | GTTTGGGGATAGGCA[C/T]GTGGCCCAAGTTGGT | 7805 |
| rs759675185 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758577 | CCATCAACTGTGCGC[C/T]AGGCCCTGGGCTAGG | 7805 |
| rs759679492 | snp | C/T | 2.83322e-05 | 0.00376368 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742410 | CTGGCCAGGGCCCTC[C/T]CTGTCCTCCTCCCCC | 7805 |
| rs759729310 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757411 | GTGAACGTCAGTTAC[A/G]TTTGCCTGGAAAGTG | 7805 |
| rs759798403 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754291 | AATCCCAGCGCGTTG[A/G]GAGGCCAAGGCAGGA | 7805 |
| rs759977615 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752764 | GTGAACTTACCTGCA[C/T]GAGGTCAGGGCAATA | 7805 |
| rs760019670 | snp | C/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733449 | TGTTTGACCAAATTA[C/T]TTTACTGAACTGACA | 7805 |
| rs760077746 | snp | A/C | 0.000457561 | 0.0151186 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739189 | AGTGACTCTCGTCCC[A/C]TGTGCACAGAGAGAC | 7805 |
| rs760137927 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748355 | CCAAGTGCCAGAGCC[C/T]TCCCTTGCCCCTCCC | 7805 |
| rs760302369 | snp | A/C | 1.6708e-05 | 0.00289028 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737706 | GAGGTAATTCTGCAA[A/C]AGATTTGGGGGCCAC | 7805 |
| rs760503123 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754998 | CCTATGGGAAAGCCC[C/T]CAGGCCCTGCCCTTT | 7805 |
| rs760605055 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747160 | ACAGGAAACCCATGA[A/G]CGTGGCTTTGAGGGG | 7805 |
| rs760820990 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735161 | CTGGCACCCACCTGC[A/G]GCCACACTCACCTTC | 7805 |
| rs760863054 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749606 | ATCCAGGCCAGAGGG[C/T]ACGACTCCCAGGGAC | 7805 |
| rs760913545 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746214 | GACCCTCATTTTCCC[C/G]TGGGGCCATTGGGAT | 7805 |
| rs761039284 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741350 | GCTTCCACCTGCCGT[C/T]TAAAAGGATGTGAGT | 7805 |
| rs761082351 | snp | C/G | 6.90679e-05 | 0.00587615 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739766 | TCTCCCATGCCAGAC[C/G]TGGGCTCTGCTGTCC | 7805 |
| rs761135343 | snp | A/C/G | 5.02604e-05 | 0.00501279 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739842 | CAACTTGAGGTAGGC[A/C/G]GGCAGCTCAATGTAG | 7805 |
| rs761216056 | in-del | -/GAGGC | 1.80637e-05 | 0.00300525 | frameshift-variant, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742545 | ACAACAAGACGCTCA[-/GAGGC]TGATCTGGAGGCAAA | 7805 |
| rs761225896 | snp | A/G | 6.59022e-05 | 0.00573993 | missense | LAPTM5 | GRCh38.p7 | 1:30735210 | CTCTTCTCCTCCACC[A/G]AGTTCATGCACTTGA | 7805 |
| rs761257463 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738337 | CGCAGGGGAAGCCAG[C/G]AGCCATGTCAGGAGA | 7805 |
| rs761275022 | snp | A/C | 3.80981e-05 | 0.00436436 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757648 | CACACACCCGGGGCC[A/C]GCACACTCACCACAT | 7805 |
| rs761313568 | snp | A/C | 0.00146924 | 0.027064 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733616 | TGAATTATGGAGAGA[A/C]CCGAGGAGTGACTCA | 7805 |
| rs761391129 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757184 | TTCTCATCCCCTCGA[C/G]TGGCCCAGGCTCCCT | 7805 |
| rs761442016 | snp | C/T | 3.17043e-05 | 0.00398135 | splice-donor-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738939 | CCTGCCCCAGACTCA[C/T]CATGTGGTTCATGGA | 7805 |
| rs761645838 | snp | A/C | 2.67133e-05 | 0.00365458 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742421 | CCTCCCTGTCCTCCT[A/C]CCCCCGCCACTCCAC | 7805 |
| rs761704013 | snp | C/T | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732593 | GACAGTCCCCAGAGA[C/T]CCTGCCTCCGTGGCC | 7805 |
| rs761949202 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742175 | AGCAGCCACTGACGG[C/T]TTTAAGCAGAAGAGT | 7805 |
| rs761986852 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750594 | CAGCTCTTTACACAT[A/G]GGCTCTGTGCTTCTC | 7805 |
| rs762072505 | snp | C/T | 1.67276e-05 | 0.00289197 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739850 | GGTAGGCGGGCAGCT[C/T]AATGTAGGAGCCCAG | 7805 |
| rs762156936 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750070 | AGTGCTGTGACTGGG[C/T]GCTAGCAGCTAACTT | 7805 |
| rs762182190 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30743232 | TCCATTATCCCCATT[C/T]GACTGTAGGTTCCAG | 7805 |
| rs762280276 | snp | C/G | 0.000183201 | 0.00956905 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733619 | ATTATGGAGAGACCC[C/G]AGGAGTGACTCAGCC | 7805 |
| rs762378064 | snp | A/C | 0.000220775 | 0.0105042 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739161 | TTGAGAGACCGTCTC[A/C]GCTACAGACATCAGT | 7805 |
| rs762482837 | snp | A/G | 8.08636e-05 | 0.00635809 | synonymous-codon, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738994 | TTCCATGTAGGAGCT[A/G]CAGAGGGTCAGGATG | 7805 |
| rs762518553 | in-del | -/GGTGA | 1.84194e-05 | 0.0030347 | splice-acceptor-variant, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742551 | AGACGCTCATGATCT[-/GGTGA]GGAGGCAAAGCAAAG | 7805 |
| rs762572720 | in-del | -/C | 0.000294737 | 0.012136 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733793 | TATGAGGCAGCTCCA[-/C]CCCTCCCAGCACTGG | 7805 |
| rs762758413 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749119 | TTTTGCAGGAAAACA[C/G]GCAAATGCATTGTGG | 7805 |
| rs762777420 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749408 | TGGGTGGAGGTCACA[C/T]GGGTGTGTTCACCTT | 7805 |
| rs762807355 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743888 | CGTGGAAAGGGACTG[A/G]ACGGAAGAGTGATGA | 7805 |
| rs762845113 | snp | A/G | 1.74327e-05 | 0.00295229 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742494 | GAGAGCTTGCAGGAC[A/G]CCTTGCCATGGGCCA | 7805 |
| rs762969146 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | LAPTM5 | GRCh38.p7 | 1:30735181 | CACTCACCTTCTGGA[A/G]CATCTTGGAGTTTCT | 7805 |
| rs763068236 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733212 | GAATTAAATGGTTTG[A/G]AGGCTAACGTGATTT | 7805 |
| rs763199829 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737188 | CCAAACCTCTATTAA[C/T]ATAATCTCAGGTACA | 7805 |
| rs763221228 | snp | G/T | 0.000172667 | 0.00928997 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733677 | TCACAGGCCCTGCAG[G/T]AGGAGCAGGCCAGCG | 7805 |
| rs763293517 | snp | C/T | 3.68813e-05 | 0.0042941 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757652 | CACCCGGGGCCCGCA[C/T]ACTCACCACATGGTA | 7805 |
| rs763415925 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737269 | TGCCCCTGAGGCCCA[C/G]AGAGAAGTGACTTGC | 7805 |
| rs763429841 | in-del | -/A | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757969 | TCTGCCATTCCCAGG[-/A]GGGGGTTCCAGAGAG | 7805 |
| rs763470804 | snp | C/T | 2.12267e-05 | 0.00325774 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742446 | CTCCACCGGCGTCCC[C/T]TGGACCTACCGATCC | 7805 |
| rs763620673 | snp | A/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751863 | TGAGGCAGGGACCAC[A/T]GGCCCCATTTACAGA | 7805 |
| rs763644118 | snp | G/T | 0.000155485 | 0.00881579 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757645 | GCACACACACCCGGG[G/T]CCCGCACACTCACCA | 7805 |
| rs763687921 | snp | G/T | 1.65627e-05 | 0.00287769 | missense | LAPTM5 | GRCh38.p7 | 1:30737605 | AGGGATCCACTCACC[G/T]TGAAGATAAGGACAG | 7805 |
| rs763767193 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753281 | AGCTACTCTGCCCTC[A/G]AGGAGGTGGGGCGGA | 7805 |
| rs763837840 | snp | C/T | 1.8102e-05 | 0.00300843 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739970 | CACCGTCAAGTGTCC[C/T]CTGCATGCAGCCAAC | 7805 |
| rs763855729 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755159 | GCTCCTGCTCTAGAA[C/T]GTCTCATCACTCATA | 7805 |
| rs763940416 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742041 | ACAGGGACAGGGTTG[A/G]TGAGGTCAGTGTGGC | 7805 |
| rs763940660 | snp | A/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755011 | CCCCAGGCCCTGCCC[A/T]TTCTGGGAAGGAGAG | 7805 |
| rs764028265 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744106 | CAGAATCTGCTTTTG[G/T]CTGGGGCAAGCTTAC | 7805 |
| rs764028281 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755940 | GCTCCCGGGGTCACC[A/G]CAGGCCCCATCTGCC | 7805 |
| rs764117825 | snp | A/C | 6.61288e-05 | 0.00574979 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741651 | TCACCTTGACTACGC[A/C]GATCAGTAGGCTCAG | 7805 |
| rs764434051 | snp | C/T | 0.000103056 | 0.00717755 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739781 | CTGGGCTCTGCTGTC[C/T]GGTGAGAGGTGGGGG | 7805 |
| rs764594879 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | LAPTM5 | GRCh38.p7 | 1:30735258 | CACACGCACTTGAAC[A/G]TGTAGACCTGGAAAA | 7805 |
| rs764679300 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749637 | CCAGCACACAGGGCT[C/G]TGGGTCAACACCCAG | 7805 |
| rs764721370 | snp | G/T | 1.64977e-05 | 0.00287203 | missense | LAPTM5 | GRCh38.p7 | 1:30737642 | AGGCGATGGAAAAGA[G/T]GATCATCATCTTGAT | 7805 |
| rs764774321 | snp | C/T | 2.93414e-05 | 0.00383012 | missense, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738951 | TCACCATGTGGTTCA[C/T]GGACTTGAAGTTGAG | 7805 |
| rs764833877 | in-del | -/G | 0.000239894 | 0.0109494 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733597 | AAACCAAGCATTGTT[-/G]GGCTGAATTATGGAG | 7805 |
| rs764939312 | snp | A/G | 5.56143e-05 | 0.00527295 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741666 | CGATCAGTAGGCTCA[A/G]GCTGATGATGAAGAG | 7805 |
| rs765070466 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748595 | TCAGAGCTTATGAGG[G/T]CTCAGTGGGGGCCAG | 7805 |
| rs765123400 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741547 | CCGCCTAACATACCC[A/G]CCTCCCACCCTCTCA | 7805 |
| rs765162080 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749099 | TGGAATCAATCCAAA[C/T]GTTATTTTGCAGGAA | 7805 |
| rs765174104 | snp | C/T | 2.60068e-05 | 0.00360593 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742424 | CCCTGTCCTCCTCCC[C/T]CCGCCACTCCACCGG | 7805 |
| rs765271074 | snp | A/G | 1.67206e-05 | 0.00289137 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739852 | TAGGCGGGCAGCTCA[A/G]TGTAGGAGCCCAGCA | 7805 |
| rs765427872 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756169 | TGCATGCCACACTGT[C/T]CTTCTAAGAATGTGC | 7805 |
| rs765518717 | snp | A/G | 5.22981e-05 | 0.00511335 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739934 | GCAGGTACTTCTCCC[A/G]GTTCTGAAAGGTAGG | 7805 |
| rs765673504 | snp | A/C/G | 0.000680928 | 0.0184396 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757649 | ACACACCCGGGGCCC[A/C/G]CACACTCACCACATG | 7805 |
| rs765676667 | snp | C/T | 2.17796e-05 | 0.0032999 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757613 | CCGCAGACATTCACA[C/T]TCACACAAGCACGCA | 7805 |
| rs765693131 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754406 | CTGGCCATGGTGGCA[C/T]GCGCCTGTGATCCTA | 7805 |
| rs765898053 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735330 | GCTCCAGCAGGCCTA[A/G]GACATATGCCAGGCA | 7805 |
| rs765954048 | in-del | -/GCAAA | 1.86733e-05 | 0.00305553 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742555 | GCTCATGATCTGGAG[-/GCAAA]GCAAAGCAAAGCATC | 7805 |
| rs766042472 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745228 | TTCCCATTTCACAGA[C/T]GAAGAAAGTGCAGCT | 7805 |
| rs766081076 | in-del | -/C | 1.65072e-05 | 0.00287286 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735146 | GAGTTAGTGACAGGG[-/C]TGGCACCCACCTGCA | 7805 |
| rs766132496 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746481 | TTCCCCTCATGTCCC[C/T]GGTTTCCACCTGGAC | 7805 |
| rs766226804 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738575 | GAAGCTGTGTGAAAT[A/C]ATAAATGTTTATTGC | 7805 |
| rs766268584 | snp | A/C | 1.74108e-05 | 0.00295044 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742495 | AGAGCTTGCAGGACG[A/C]CTTGCCATGGGCCAC | 7805 |
| rs766270579 | snp | C/T | 1.77846e-05 | 0.00298194 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733928 | ACCACCTGGGAGAGA[C/T]AGAGAGATGAGGGCT | 7805 |
| rs766304668 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756309 | TTCCTCCTCCCAAAA[C/T]TAGAGTCCTTGAATC | 7805 |
| rs766309830 | snp | C/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758899 | TGCAATGCCAAGCTT[C/G]TAGTGCAGAGCAGAC | 7805 |
| rs766316469 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739566 | TGGGCTGCACCCCCA[A/G]TGTGTGTGTTCCTCA | 7805 |
| rs766323570 | snp | C/T | 1.64841e-05 | 0.00287085 | missense | LAPTM5 | GRCh38.p7 | 1:30735182 | ACTCACCTTCTGGAG[C/T]ATCTTGGAGTTTCTC | 7805 |
| rs766399521 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752863 | TCAGGCTAGAGCGCA[A/G]TGGCGCGATCTCGGC | 7805 |
| rs766591809 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744359 | CAGTTTCACCTTGAA[C/T]GAGAGAAAGAGAAAG | 7805 |
| rs766623674 | snp | A/G | 1.84752e-05 | 0.00303929 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733823 | GGGCTGGGGCCTGGC[A/G]AGGGTCACACCTCTG | 7805 |
| rs766748661 | snp | A/G | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743665 | CCCTCCCCTCTAGTC[A/G]GTGCCCTATCTCTAT | 7805 |
| rs766751707 | snp | A/G | 5.26561e-05 | 0.00513081 | missense | LAPTM5 | GRCh38.p7 | 1:30757664 | GCACACTCACCACAT[A/G]GTAGATGGCCAGGGC | 7805 |
| rs766797272 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750774 | CTGTTTCCTCATCTG[C/T]AAAATGGAGGCCCCC | 7805 |
| rs766815312 | snp | C/T | 6.19233e-05 | 0.00556398 | synonymous-codon, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739027 | CAGGCAGAAGTCCAG[C/T]AGCTGCAGCGTCATC | 7805 |
| rs766873943 | in-del | -/G | | | frameshift-variant | LAPTM5 | GRCh38.p7 | 1:30737669 | TGATGAACTGGTTAT[-/G]AGGCATATCCTCCTG | 7805 |
| rs767047113 | in-del | -/ACCA | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733529 | TTGCTTGACAAACTC[-/ACCA]ACCAACTTTAGAATG | 7805 |
| rs767204500 | snp | A/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747125 | ATTGCTGTCTAAAAA[A/T]CTTAGGGAGAATTTC | 7805 |
| rs767204897 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735579 | CCTGGAAGCTCACTA[A/C]CTCCTGAGACAGCCC | 7805 |
| rs767217599 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30735188 | CTTCTGGAGCATCTT[A/G]GAGTTTCTCTTCTCC | 7805 |
| rs767288360 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737588 | TCCCAGAGCCGCAGG[C/G]CAGGGATCCACTCAC | 7805 |
| rs767456297 | in-del | -/GTGA | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732285 | GGGTGTGGGGAGGGT[-/GTGA]GTGTGTGGGTATGTG | 7805 |
| rs767458489 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754732 | CCGAGCCCAAAGCTA[C/T]GGACCAGGCTTCCCT | 7805 |
| rs767520995 | snp | C/T | 1.78481e-05 | 0.00298726 | missense | LAPTM5 | GRCh38.p7 | 1:30733833 | CTGGCGAGGGTCACA[C/T]CTCTGAGTATGGGGG | 7805 |
| rs767625544 | in-del | -/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758673 | GCCTCAAGACCCAAT[-/C]CCCATACTCACACAA | 7805 |
| rs767643820 | snp | G/T | 3.4665e-05 | 0.00416309 | missense | LAPTM5 | GRCh38.p7 | 1:30733908 | CTTCCTCGTAGGACG[G/T]CAGGACCACCTGGGA | 7805 |
| rs767770902 | snp | A/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758688 | CCCCATACTCACACA[A/C]AATCAGGGATTGCTT | 7805 |
| rs767785850 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749546 | CTGTGCCAGGTTCCA[C/T]GGGATCATGAAGATG | 7805 |
| rs768030377 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733481 | GTGGGTTTTTGATTT[A/G]TCAGTTGCTTGGCTG | 7805 |
| rs768047470 | snp | C/G/T | 3.45502e-05 | 0.00415622 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739765 | ATCTCCCATGCCAGA[C/G/T]CTGGGCTCTGCTGTC | 7805 |
| rs768113766 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749027 | CAGGTGCCTGTGTGT[A/G]GACACCCAGCACGGA | 7805 |
| rs768216676 | snp | C/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758015 | GGTCATCATGCCCTT[C/G]TCTGCACCAGGGCCA | 7805 |
| rs768222910 | snp | C/G | 0.000259297 | 0.0113834 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733807 | ACCCCTCCCAGCACT[C/G]GGGCTGGGGCCTGGC | 7805 |
| rs768364671 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749330 | GGCAGAAGTCAGTGG[A/G]GGCGGGGCAGTGGCG | 7805 |
| rs768410389 | snp | C/G | 1.74931e-05 | 0.0029574 | missense | LAPTM5 | GRCh38.p7 | 1:30733845 | ACACCTCTGAGTATG[C/G]GGGTGGTGCTGGGCC | 7805 |
| rs768440483 | snp | A/G | 0.000167406 | 0.0091474 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738932 | ATGGTTCCCTGCCCC[A/G]GACTCACCATGTGGT | 7805 |
| rs768481058 | snp | A/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30732519 | GTCGCACACAAAGCA[A/G]TTACACAAGGGGGTA | 7805 |
| rs768716899 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751364 | GACATAAAGGTGGCA[A/G]GTTCTAACAGATTCT | 7805 |
| rs768726812 | snp | C/T | 1.68052e-05 | 0.00289867 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737570 | GCACAGCCTCACCAC[C/T]CCTCCCAGAGCCGCA | 7805 |
| rs768788733 | snp | A/T | 1.81251e-05 | 0.00301036 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742546 | ACAACAAGACGCTCA[A/T]GATCTGGAGGCAAAG | 7805 |
| rs768836998 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30735248 | GTAGCACCGCCACAC[A/G]CACTTGAACATGTAG | 7805 |
| rs768949774 | snp | A/G | 8.4679e-05 | 0.00650633 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739912 | ATTTGCAGGGACAGG[A/G]AGGGCAGCAGGTACT | 7805 |
| rs768962621 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751270 | CACCCTGCCCCCACC[A/G]GCCTCCTCACCCCTC | 7805 |
| rs769030764 | in-del | -/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759584 | GGTAAACATTTCTCA[-/T]TTTTTTATGGTGATA | 7805 |
| rs769043815 | snp | A/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739423 | CACTGGCATGAATCA[A/T]CCTTCTCTTCCTTTC | 7805 |
| rs769093065 | in-del | -/G | 1.81251e-05 | 0.00301036 | frameshift-variant, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742546 | CAACAAGACGCTCAT[-/G]GATCTGGAGGCAAAG | 7805 |
| rs769108048 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30736158 | CATGAGGCCTTCAGG[A/G]GTGTTCTCACTGTAC | 7805 |
| rs769318025 | snp | C/T | 0.000183638 | 0.00958046 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733617 | GAATTATGGAGAGAC[C/T]CGAGGAGTGACTCAG | 7805 |
| rs769341761 | snp | A/G | 1.6955e-05 | 0.00291157 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30757722 | GCAGCAGGTCTGGCG[A/G]ACAGTGGACAAGCGG | 7805 |
| rs769466101 | snp | C/T | 0.000197258 | 0.00992926 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739155 | CCTCACTTGAGAGAC[C/T]GTCTCAGCTACAGAC | 7805 |
| rs769516896 | snp | C/T | 3.36887e-05 | 0.00410405 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739817 | TACTCACAGCACGGC[C/T]CCGGGAGGCCAACTT | 7805 |
| rs769709162 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734817 | CTTCCCTGATACCTG[A/G]GAAGAGGCCAGGTCC | 7805 |
| rs769873607 | snp | A/G | 1.87106e-05 | 0.00305859 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742465 | ACCTACCGATCCTGA[A/G]GTAGCCCATCTGGGA | 7805 |
| rs769976242 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751381 | TTCTAACAGATTCTC[A/G]CCCAGGGTTTTCCCC | 7805 |
| rs769983309 | snp | C/T | 8.12909e-05 | 0.00637486 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741637 | GGGCTCCTGAGCCCT[C/T]ACCTTGACTACGCCG | 7805 |
| rs770066352 | snp | A/G | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743311 | TTGTTGAATGAATGA[A/G]TGAATGAATGAATGA | 7805 |
| rs770248460 | snp | C/T | 3.70048e-05 | 0.00430128 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741745 | AGAGCAGGGAGGTGC[C/T]CAGGGGTGCCCCTGG | 7805 |
| rs770290975 | snp | A/C | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30757944 | CCTGCCTCAGAGCAC[A/C]CCACTGCCCTCTGCC | 7805 |
| rs770301183 | snp | C/T | 1.71605e-05 | 0.00292915 | missense | LAPTM5 | GRCh38.p7 | 1:30733895 | GGCAAAGACAGGGCT[C/T]CCTCGTAGGACGGCA | 7805 |
| rs770403585 | snp | A/G | 3.19066e-05 | 0.00399403 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739167 | GACCGTCTCAGCTAC[A/G]GACATCAGTGACTCT | 7805 |
| rs770409083 | snp | A/G | 1.67812e-05 | 0.0028966 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739828 | CGGCTCCGGGAGGCC[A/G]ACTTGAGGTAGGCGG | 7805 |
| rs770421312 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739653 | AAGAAACTTGGGGCA[A/G]TGTGGAGGGACTCAG | 7805 |
| rs770473268 | in-del | -/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747275 | CAGGTGTGTTTCAGT[-/C]CCTTCAGGGAAACTC | 7805 |
| rs770591376 | snp | C/T | 1.67158e-05 | 0.00289096 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739881 | CAGGGTGAGCAGGCA[C/T]AGGAGATAGTCCATG | 7805 |
| rs770659339 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747033 | CAGTCTCCAGGGAAC[C/T]CGATACATGAATGGT | 7805 |
| rs770697644 | snp | A/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749414 | GAGGTCACATGGGTG[A/T]GTTCACCTTGTAGAA | 7805 |
| rs770817535 | snp | C/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741012 | CAGGGACCGCGGGTT[C/G]CTCTTCTGCAGGGGA | 7805 |
| rs770995931 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734972 | TGAGACTAGCAAAGA[A/G]TGAGAGGCAGTAAAT | 7805 |
| rs771019420 | snp | A/G | 3.29799e-05 | 0.00406065 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735280 | CCTGGAAAAAGGCCC[A/G]GGTCAGGCTGTGCTT | 7805 |
| rs771048652 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734720 | TCATCCTCTCTTCCC[A/G]GAAAGCCTCCTTCTG | 7805 |
| rs771086027 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744447 | TCCCTGTTCCTGGGA[A/G]TATGTAAGCAGATCA | 7805 |
| rs771177022 | snp | A/C | 1.6498e-05 | 0.00287206 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742405 | TATCCCTGGCCAGGG[A/C]CCTCCCTGTCCTCCT | 7805 |
| rs771232239 | snp | A/G | 1.7274e-05 | 0.00293883 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733903 | CAGGGCTTCCTCGTA[A/G]GACGGCAGGACCACC | 7805 |
| rs771262736 | in-del | -/C | 3.05885e-05 | 0.00391067 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742420 | CCTCCCTGTCCTCCT[-/C]CCCCCCGCCACTCCA | 7805 |
| rs771355171 | snp | C/T | 2.04175e-05 | 0.00319505 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733966 | GTCAAGAATGACCTG[C/T]AATTCCAACCTGGGG | 7805 |
| rs771385855 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752447 | ACCCAGCTTGACAAA[C/T]CTGCTAGGTCTCTGA | 7805 |
| rs771650879 | snp | A/G | 1.67363e-05 | 0.00289272 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739887 | GAGCAGGCACAGGAG[A/G]TAGTCCATGATTTGC | 7805 |
| rs771717894 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748784 | TCGTCCTCACCCGCC[A/G]CCTCCACCTCATCCC | 7805 |
| rs771756857 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756861 | AGGAGTTTGGGAGTA[A/G]GGTGGGTCTAGGCAG | 7805 |
| rs771810554 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737276 | GAGGCCCAGAGAGAA[C/G]TGACTTGCTGAAGAC | 7805 |
| rs771836666 | snp | A/C | 2.01558e-05 | 0.00317451 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757640 | CGCACGCACACACAC[A/C]CGGGGCCCGCACACT | 7805 |
| rs771841953 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742752 | CTGGGTCTTCCTCTC[G/T]CCAGCTATGTGACCC | 7805 |
| rs771865800 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748249 | CTCCTCCTACCAAAT[A/G]TGCGAGCCCAGGACA | 7805 |
| rs771874650 | snp | A/G | 3.81294e-05 | 0.00436615 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738915 | ACAGCCAGCAAATGG[A/G]CATGGTTCCCTGCCC | 7805 |
| rs771889622 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741833 | GATGCACAGGAAAGC[C/T]CAGGCCCTGCCCTCT | 7805 |
| rs771979191 | snp | C/T | 1.64925e-05 | 0.00287158 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742415 | CAGGGCCCTCCCTGT[C/T]CTCCTCCCCCCGCCA | 7805 |
| rs772036993 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750496 | TGACCATACACTCTC[C/T]CGTGTCAACCTCGCG | 7805 |
| rs772123627 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735897 | TTTGATGGATTCCCT[C/G]ATGGGCACATAGGTG | 7805 |
| rs772176565 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746859 | GAATCGTGTGGTGCG[C/T]GGAGCCGGGCACACA | 7805 |
| rs772252143 | snp | C/G | 1.65067e-05 | 0.00287282 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735144 | GGGAGTTAGTGACAG[C/G]GCTGGCACCCACCTG | 7805 |
| rs772253448 | snp | A/G | 2.08753e-05 | 0.00323067 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742448 | CCACCGGCGTCCCCT[A/G]GACCTACCGATCCTG | 7805 |
| rs772374354 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749977 | TGCAGGAGATGTGAC[A/G]GCTCATGCAAAACCT | 7805 |
| rs772379976 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | LAPTM5 | GRCh38.p7 | 1:30735234 | CACTTGATCAATCTG[C/T]AGCACCGCCACACGC | 7805 |
| rs772432930 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759694 | AAAGTCTCATTTTAA[A/G]AGAAATGCATTTAAA | 7805 |
| rs772510247 | in-del | -/ACCT | 4.14276e-05 | 0.00455105 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742450 | ACCGGCGTCCCCTGG[-/ACCT]ACCGATCCTGAGGTA | 7805 |
| rs772542944 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752524 | CCCGCCCAGCGTGAC[C/T]TCTTTTCCAAGGTGC | 7805 |
| rs772561163 | snp | C/T | 1.7315e-05 | 0.00294231 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742525 | CCTCTACTGAGTGCT[C/T]GATGAACAACAAGAC | 7805 |
| rs772612127 | snp | G/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741072 | CCAGATTTGCCTCGG[G/T]CCCAGGAGCCCCTCG | 7805 |
| rs772649930 | snp | G/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740977 | TGGTGAGGCCCTGGC[G/T]TCCTGCCTTTCTGGG | 7805 |
| rs772728976 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758766 | TAGGCAAGCTACCCT[A/G]GAATCTCTACTCCCT | 7805 |
| rs772743501 | snp | A/C | 1.82994e-05 | 0.00302479 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757789 | TGAAGGGGAAAGAGC[A/C]TGGTGCCTGGAGCAG | 7805 |
| rs772768097 | in-del | -/CCA | 1.83555e-05 | 0.00302943 | splice-acceptor-variant, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742550 | AAGACGCTCATGATC[-/CCA]TGGAGGCAAAGCAAA | 7805 |
| rs772801469 | snp | C/T | 4.94923e-05 | 0.0049743 | missense | LAPTM5 | GRCh38.p7 | 1:30737649 | GGAAAAGATGATCAT[C/T]ATCTTGATGAACTGG | 7805 |
| rs772949461 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749109 | CCAAATGTTATTTTG[C/T]AGGAAAACAGGCAAA | 7805 |
| rs772996891 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754554 | AAAACAAAAACAAAA[C/T]AAAACAAATCAAACC | 7805 |
| rs773050225 | snp | C/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753585 | TTTGACAAAATGCCT[C/G]ACAAATACTCCTCGA | 7805 |
| rs773065499 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757273 | ACAATCCCAGCCCAC[A/G]TTCCTCCCAAGATCC | 7805 |
| rs773084843 | snp | A/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749091 | CCCCAAGCTGGAATC[A/T]ATCCAAATGTTATTT | 7805 |
| rs773129175 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739492 | GGGGGCTAAAAAGCG[C/T]ACATGTCCTTTCCTC | 7805 |
| rs773246740 | snp | G/T | 3.51432e-05 | 0.0041917 | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739945 | TCCCGGTTCTGAAAG[G/T]TAGGCCCAGCACCGT | 7805 |
| rs773264858 | snp | A/C | 1.64846e-05 | 0.0028709 | missense | LAPTM5 | GRCh38.p7 | 1:30735176 | AGCCACACTCACCTT[A/C]TGGAGCATCTTGGAG | 7805 |
| rs773485623 | snp | A/G | 3.72488e-05 | 0.00431544 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741643 | CTGAGCCCTCACCTT[A/G]ACTACGCCGATCAGT | 7805 |
| rs773507207 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744385 | GAAAGGGAGGCAGAT[A/G]ACAGCTCCGTCCAGC | 7805 |
| rs773588688 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751408 | CCCCACCTGGCAGTT[C/T]GGACCCATTTTTCAA | 7805 |
| rs773601185 | snp | A/G | 5.64477e-05 | 0.00531231 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733820 | CTGGGGCTGGGGCCT[A/G]GCGAGGGTCACACCT | 7805 |
| rs773649946 | snp | G/T | 1.64749e-05 | 0.00287005 | missense | LAPTM5 | GRCh38.p7 | 1:30757729 | GTCTGGCGGACAGTG[G/T]ACAAGCGGGGGTCCA | 7805 |
| rs773820075 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750608 | TGGGCTCTGTGCTTC[C/T]CAGAACAAGGCTCTG | 7805 |
| rs773891848 | snp | A/T | 3.35368e-05 | 0.00409479 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739834 | CGGGAGGCCAACTTG[A/T]GGTAGGCGGGCAGCT | 7805 |
| rs773952313 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749975 | CATGCAGGAGATGTG[A/G]CGGCTCATGCAAAAC | 7805 |
| rs773983150 | snp | C/T | 2.27663e-05 | 0.00337382 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742588 | TCAGCTGAGCCTGCA[C/T]CACGGCCCCCCGACC | 7805 |
| rs774236842 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734214 | TCAGAAGAACTGGTC[C/G]CATCCCTCAGATCCA | 7805 |
| rs774242758 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750309 | CCTTTATCTTCAGAG[C/T]AAAGACCCACAATAG | 7805 |
| rs774359674 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745975 | GCCTCTCTCCTGGGG[C/T]CAGGGCTCCCCACAA | 7805 |
| rs774378981 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735284 | GAAAAAGGCCCAGGT[C/T]AGGCTGTGCTTTGCT | 7805 |
| rs774512442 | snp | C/T | 2.83595e-05 | 0.0037655 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742409 | CCTGGCCAGGGCCCT[C/T]CCTGTCCTCCTCCCC | 7805 |
| rs774563716 | snp | C/T | 5.18829e-05 | 0.00509301 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733906 | GGCTTCCTCGTAGGA[C/T]GGCAGGACCACCTGG | 7805 |
| rs774668460 | snp | A/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735018 | GAGTGAGTGAATGAA[A/T]CTTAGACTACCAGAA | 7805 |
| rs774686280 | snp | C/T | 1.65203e-05 | 0.002874 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735127 | TTGACCCAAATGGCA[C/T]AGGGAGTTAGTGACA | 7805 |
| rs774791340 | snp | C/T | 0.000261063 | 0.011422 | intron-variant, nc-transcript-variant | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739170 | CGTCTCAGCTACAGA[C/T]ATCAGTGACTCTCGT | 7805 |
| rs774795880 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739453 | CTTCAACTTGGTTCC[A/G]AAGAAGAAATAATAC | 7805 |
| rs774835687 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744476 | CACAGATGAGTCACA[A/G]CTGGGCTTAGAGAAG | 7805 |
| rs775001353 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748330 | GACAATGCAGTTTGC[C/T]ATATGGGTCCCAAGT | 7805 |
| rs775075793 | snp | C/T | 6.01425e-05 | 0.0054834 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757641 | GCACGCACACACACC[C/T]GGGGCCCGCACACTC | 7805 |
| rs775127366 | snp | A/C | 6.60917e-05 | 0.00574817 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733615 | CTGAATTATGGAGAG[A/C]CCCGAGGAGTGACTC | 7805 |
| rs775154709 | snp | C/G | 2.49672e-05 | 0.00353313 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742593 | TGAGCCTGCATCACG[C/G]CCCCCCGACCAGCCC | 7805 |
| rs775255797 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738033 | TTGGCTGACAGGGAC[A/C]ACCTAATCCACTAAT | 7805 |
| rs775337739 | snp | A/C | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30754964 | TCAAGGTCCTATCAG[A/C]ACACCTGTTGCCAGC | 7805 |
| rs775459865 | snp | A/G | 7.02198e-05 | 0.00592494 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738927 | TGGGCATGGTTCCCT[A/G]CCCCAGACTCACCAT | 7805 |
| rs775490583 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755866 | CCACCAGGGCCCACA[A/G]TCCTTCGTGGCAACA | 7805 |
| rs775619291 | snp | A/G | 1.74406e-05 | 0.00295296 | synonymous-codon | LAPTM5 | GRCh38.p7 | 1:30733911 | CCTCGTAGGACGGCA[A/G]GACCACCTGGGAGAG | 7805 |
| rs775659406 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759724 | ATAAAAAAGGCAGTA[A/G]GTCAATTTAAAGAAC | 7805 |
| rs775768286 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744853 | ACCTTTTGCACACAC[A/G]CCTCTATTTTTCTTT | 7805 |
| rs775780861 | snp | A/C | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30741219 | GCATGGATAGAGCTG[A/C]ATGCATCCTACTTTC | 7805 |
| rs775820379 | in-del | -/AGAGAGGTGGG | 1.79754e-05 | 0.0029979 | frameshift-variant, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742543 | GAACAACAAGACGCT[-/AGAGAGGTGGG]CATGATCTGGAGGCA | 7805 |
| rs775833462 | in-del | -/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30748916 | TGTAACATTTCCTCA[-/T]CTGTAGAAGGGAGAG | 7805 |
| rs775906591 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750007 | TAGAGAACCTAGACT[C/T]GGACGGCTCAGATGG | 7805 |
| rs775962375 | in-del | -/AG | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755894 | ACAACAAGCAAAAAC[-/AG]AGAACAGCTGCAGGG | 7805 |
| rs776021699 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746212 | GAGACCCTCATTTTC[A/C]CCTGGGGCCATTGGG | 7805 |
| rs776089130 | snp | C/T | 1.9328e-05 | 0.00310863 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757646 | CACACACACCCGGGG[C/T]CCGCACACTCACCAC | 7805 |
| rs776147713 | snp | G/T | 1.681e-05 | 0.00289909 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739901 | GATAGTCCATGATTT[G/T]CAGGGACAGGAAGGG | 7805 |
| rs776148998 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741502 | GTTCTCCAAAAGGTA[C/T]GTGTGAAGATCTCCA | 7805 |
| rs776216936 | snp | A/G | 9.92507e-05 | 0.00704383 | missense | LAPTM5 | GRCh38.p7 | 1:30737611 | CCACTCACCTTGAAG[A/G]TAAGGACAGTGATGA | 7805 |
| rs776331276 | snp | A/T | 3.24428e-05 | 0.00402745 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30738936 | TTCCCTGCCCCAGAC[A/T]CACCATGTGGTTCAT | 7805 |
| rs776358189 | snp | C/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30755961 | CCCATCTGCCCCCTG[C/G]TGTCACTCACATGGC | 7805 |
| rs776388748 | snp | C/T | 4.58096e-05 | 0.00478568 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739140 | CGGCACATAGTAGGC[C/T]CTCACTTGAGAGACC | 7805 |
| rs776530391 | snp | C/T | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750586 | ATTGAAATCAGCTCT[C/T]TACACATGGGCTCTG | 7805 |
| rs776698879 | snp | C/T | 2.72699e-05 | 0.00369245 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742419 | GCCCTCCCTGTCCTC[C/T]TCCCCCCGCCACTCC | 7805 |
| rs776789935 | snp | A/G | 3.30011e-05 | 0.00406195 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735304 | TGTGCTTTGCTGAGC[A/G]TCCTTCTCACGCTCC | 7805 |
| rs776812524 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752605 | ATTCCAGAATCCCAA[C/T]CTCCAGCCCTACATC | 7805 |
| rs776827367 | in-del | -/TGAA | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743303 | GTTGTATTTGTTGAA[-/TGAA]TGAATGAATGAATGA | 7805 |
| rs776954978 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751294 | ACCCCTCCGTGAAGC[A/G]CACAGAGCTGCAGTG | 7805 |
| rs776985936 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30746890 | GCAGGTGCACCATAA[A/G]CAAGCACAATTGGGT | 7805 |
| rs777020746 | snp | A/G | 0.000593426 | 0.0172151 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739914 | TTGCAGGGACAGGAA[A/G]GGCAGCAGGTACTTC | 7805 |
| rs777207183 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750393 | TCTTCTGAACTTATA[C/T]AGTCGGCCCTCTGTA | 7805 |
| rs777235335 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754287 | CTGTAATCCCAGCGC[A/G]TTGGGAGGCCAAGGC | 7805 |
| rs777279768 | snp | A/G/T | 5.76877e-05 | 0.00537039 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733815 | CAGCACTGGGGCTGG[A/G/T]GCCTGGCGAGGGTCA | 7805 |
| rs777435891 | snp | A/G | 0.000106039 | 0.00728067 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741647 | GCCCTCACCTTGACT[A/G]CGCCGATCAGTAGGC | 7805 |
| rs777614266 | snp | C/T | 1.67186e-05 | 0.0028912 | synonymous-codon, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739866 | AATGTAGGAGCCCAG[C/T]AGGGTGAGCAGGCAC | 7805 |
| rs777682745 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749803 | ACGCATTCAGGAAAC[A/G]GCAAGACGTTCCTCT | 7805 |
| rs777684392 | in-del | -/G | | | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733142 | ATTAACAATTATACA[-/G]CCACTCAGAGGTCCT | 7805 |
| rs777713534 | snp | A/T | 2.16551e-05 | 0.00329045 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733699 | AGGCCAGCGAGGGAG[A/T]CACAAGCAGATTGTC | 7805 |
| rs777771599 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735650 | TTCAAAATTGCTTCC[A/G]ATATGTTGTTTTCTG | 7805 |
| rs777806605 | snp | C/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759288 | GGCCTGGGATCTTCT[C/G]GCTGGGTAGGCAGAA | 7805 |
| rs777826611 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30745630 | CAGGGGACCAGCCCA[C/T]AGTCACAGAGCGAGG | 7805 |
| rs777833323 | snp | A/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751004 | GGGAAACCAACGCTC[A/G]CCTCACAGTGAGCTC | 7805 |
| rs777848573 | in-del | -/ACTG | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739532 | TTCACTCCCAGCAGC[-/ACTG]ACTGAGTGCTGACCA | 7805 |
| rs777888487 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753237 | GGAGTACAGACAAAT[C/T]TCCTTGAGAAATTCC | 7805 |
| rs777890604 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749686 | AGGGGTCAGGGCGGG[C/T]TTCTCAGAGGAGGTG | 7805 |
| rs777899514 | snp | G/T | 1.73483e-05 | 0.00294514 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757751 | GGGGGTCCATGGTGC[G/T]GCCGTCCCCTCCTCT | 7805 |
| rs777950944 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757402 | AGCCTCGGAGTGAAC[A/G]TCAGTTACATTTGCC | 7805 |
| rs777988961 | snp | A/G | 1.72202e-05 | 0.00293424 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737742 | TGTCTCTGGACATAA[A/G]GAATTCCAACAGCAC | 7805 |
| rs778042983 | snp | A/G | 6.46391e-05 | 0.00568466 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739083 | GAGGACAAATACAAG[A/G]AGGAGGAATGAGGAG | 7805 |
| rs778086367 | snp | A/T | 3.7924e-05 | 0.00435437 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741747 | AGCAGGGAGGTGCTC[A/T]GGGGTGCCCCTGGGA | 7805 |
| rs778166809 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744894 | TACACGCATGTGTTG[A/C]TGTCCTAGTTTATCA | 7805 |
| rs778361255 | snp | G/T | 1.96918e-05 | 0.00313776 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733960 | AGTATGGTCAAGAAT[G/T]ACCTGCAATTCCAAC | 7805 |
| rs778393608 | snp | G/T | 1.67178e-05 | 0.00289113 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739883 | GGGTGAGCAGGCACA[G/T]GAGATAGTCCATGAT | 7805 |
| rs778456064 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737982 | AGGTGTCAGCTGCCC[A/G]TGGGCCACACCTATG | 7805 |
| rs778491128 | snp | A/G | 0.000168848 | 0.00918669 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733692 | GAGGAGCAGGCCAGC[A/G]AGGGAGACACAAGCA | 7805 |
| rs778612735 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756816 | ACCCCAGGAGGAAGT[C/T]GCTTGGGTCTAGGGG | 7805 |
| rs778635417 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743891 | GGAAAGGGACTGAAC[A/G]GAAGAGTGATGAAGA | 7805 |
| rs778641610 | snp | A/G | 0.0002414 | 0.0109837 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741605 | GTGTGAATAACAGGA[A/G]GGGGCAGGGGGCAGC | 7805 |
| rs778724561 | snp | A/G | 1.69444e-05 | 0.00291066 | | | GRCh38.p7 | 1:30757689 | CAGGGCGGTGGTTGC[A/G]ATGCGGACATTGAAG | 7805 |
| rs778766278 | snp | A/G | 2.28574e-05 | 0.00338056 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733782 | AAAAAGCAGATTATG[A/G]GGCAGCTCCACCCCT | 7805 |
| rs778893813 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754182 | CCACTTTCTACCATC[A/G]ACTTAGAACGTGCTT | 7805 |
| rs778984144 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735781 | GGCAGAAGCTTTCCA[A/G]AGTGGGGCATACAAT | 7805 |
| rs778986551 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30753616 | ACTGTCAAGATTATC[A/G]AAAACAAGAAAAATC | 7805 |
| rs779112565 | snp | C/G | 2.18129e-05 | 0.00330242 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742443 | CCACTCCACCGGCGT[C/G]CCCTGGACCTACCGA | 7805 |
| rs779235942 | snp | A/G | 1.75511e-05 | 0.0029623 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742534 | AGTGCTCGATGAACA[A/G]CAAGACGCTCATGAT | 7805 |
| rs779344962 | in-del | -/C | 3.05885e-05 | 0.00391067 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742421 | CCTCCCTGTCCTCCT[-/C]CCCCCGCCACTCCAC | 7805 |
| rs779371071 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756999 | GAACCAGTGACAGCC[A/G]TGACTTCACAAGTTG | 7805 |
| rs779400861 | snp | G/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732334 | TTTGGGTGTATTTGT[G/T]GGTGTGTGGGGGTGG | 7805 |
| rs779593526 | snp | C/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740907 | GCCCTGCAAGGGCCA[C/G]GCCCCTGTCTGCACA | 7805 |
| rs779644407 | snp | C/T | | | missense | LAPTM5 | GRCh38.p7 | 1:30733893 | ATGGCAAAGACAGGG[C/T]TTCCTCGTAGGACGG | 7805 |
| rs779656872 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749406 | TTTGGGTGGAGGTCA[A/C]ATGGGTGTGTTCACC | 7805 |
| rs779751267 | snp | C/T | 4.19762e-05 | 0.00458109 | utr-variant-3-prime | LAPTM5 | GRCh38.p7 | 1:30733794 | ATGAGGCAGCTCCAC[C/T]CCTCCCAGCACTGGG | 7805 |
| rs779757770 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734653 | AGGTGAGGAAAGTAA[A/G]TTACCAGGAATTTAA | 7805 |
| rs779810690 | snp | A/G | 2.60196e-05 | 0.00360682 | synonymous-codon, intron-variant | LAPTM5 | GRCh38.p7 | 1:30741679 | CAGGCTGATGATGAA[A/G]AGCATGGTGATGAGC | 7805 |
| rs779865690 | snp | A/C | 3.44477e-05 | 0.00415002 | missense | LAPTM5 | GRCh38.p7 | 1:30733863 | GTGGTGCTGGGCCCC[A/C]CTCTGGGGTCTTCGA | 7805 |
| rs779869048 | snp | C/G/T | 0.000484988 | 0.0155657 | intron-variant, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739125 | GTCCCAGTTACTGAG[C/G/T]GGCACATAGTAGGCC | 7805 |
| rs779928513 | snp | C/T | 1.74934e-05 | 0.00295743 | utr-variant-5-prime | LAPTM5 | GRCh38.p7 | 1:30757758 | CATGGTGCTGCCGTC[C/T]CCTCCTCTGAGACAC | 7805 |
| rs780120735 | snp | C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747551 | TTATTCCCGTCTGCA[C/T]GCAGCCTTTCTTTCT | 7805 |
| rs780143652 | snp | A/C | 4.27981e-05 | 0.00462571 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757624 | CACACTCACACAAGC[A/C]CGCACGCACACACAC | 7805 |
| rs780174981 | snp | A/C | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752137 | CCCAGACAGACACAC[A/C]ACCCCAGCCATGGGG | 7805 |
| rs780226089 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737819 | ACAGCGTGGCACAGC[C/T]GTCACCTTGGTCGAC | 7805 |
| rs780267330 | snp | C/T | 1.65201e-05 | 0.00287398 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30735317 | GCGTCCTTCTCACGC[C/T]CCAGCAGGCCTAGGA | 7805 |
| rs780272057 | snp | C/T | 1.78436e-05 | 0.00298688 | missense, intron-variant | LAPTM5 | GRCh38.p7 | 1:30742540 | CGATGAACAACAAGA[C/T]GCTCATGATCTGGAG | 7805 |
| rs780340871 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30741556 | ATACCCGCCTCCCAC[C/T]CTCTCAGCACCCAGC | 7805 |
| rs780469705 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30754376 | GTCTCTACAAAAAAA[A/G/T]ATATTTAAAATTAGC | 7805 |
| rs780551299 | snp | A/C | 4.84602e-05 | 0.00492217 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30742435 | TCCCCCCGCCACTCC[A/C]CCGGCGTCCCCTGGA | 7805 |
| rs780626134 | snp | A/G | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759106 | TCTCCATGTGCCAAT[A/G]AGACCAAGGGGACTC | 7805 |
| rs780789867 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30750143 | ATATTCTGGCTGGTG[A/G]TAGCTTATCAAATCT | 7805 |
| rs780833255 | snp | A/G | 5.13211e-05 | 0.00506536 | missense | LAPTM5 | GRCh38.p7 | 1:30733877 | CCCTCTGGGGTCTTC[A/G]ATGGCAAAGACAGGG | 7805 |
| rs780842930 | snp | A/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30749731 | TTCCCCGAAAGAGCA[A/G]TGGAAAAAGTGTTCC | 7805 |
| rs780864966 | snp | A/G | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740762 | CAGCCACCCTGCACA[A/G]GGCAAACGGCCTCCC | 7805 |
| rs780886092 | snp | A/G | 0.000162738 | 0.00901902 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30733939 | GAGACAGAGAGATGA[A/G]GGCTGAGTATGGTCA | 7805 |
| rs780937685 | in-del | -/CAGGGGGAA | 3.39818e-05 | 0.00412186 | cds-indel, downstream-variant-500B | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739042 | CAGCTGCAGCGTCAT[-/CAGGGGGAA]CTTGGAGGAGCTCTG | 7805 |
| rs780975087 | snp | C/T | | | intron-variant, upstream-variant-2KB | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752954 | TTGGACTACAGGCTC[C/T]CGCCATCATGCCCAG | 7805 |
| rs781067463 | snp | C/T | 6.75117e-05 | 0.00580959 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739813 | TGGGTACTCACAGCA[C/T]GGCTCCGGGAGGCCA | 7805 |
| rs781072167 | snp | C/G | | | intron-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30751299 | TCCGTGAAGCGCACA[C/G]AGCTGCAGTGGCAGA | 7805 |
| rs781074378 | snp | C/G | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744284 | CTCACAGGAAACAGC[C/G]CTGAGAGAAAAAAAC | 7805 |
| rs781106228 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30758153 | GGTCAAGGCACTTGC[C/T]CCAAATCACACAGTA | 7805 |
| rs781116816 | snp | A/G | 5.01576e-05 | 0.00500762 | missense, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30739858 | GGCAGCTCAATGTAG[A/G]AGCCCAGCAGGGTGA | 7805 |
| rs781259206 | snp | A/C/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30752289 | GCTGGACCTGTTTTC[A/C/T]CATCTGCAAAATGAG | 7805 |
| rs781309185 | snp | A/C/T | 1.70959e-05 | 0.00292364 | missense | LAPTM5 | GRCh38.p7 | 1:30733878 | CCTCTGGGGTCTTCG[A/C/T]TGGCAAAGACAGGGC | 7805 |
| rs781329365 | in-del | -/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738234 | GCTGGACTTAGCAAC[-/T]GCACTTCTAACTAAC | 7805 |
| rs781391842 | snp | C/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737935 | TCCAGATCTGCTTCC[C/T]AGGCTGGCGCACCGG | 7805 |
| rs781395344 | snp | C/T | 2.11218e-05 | 0.00324968 | intron-variant | LAPTM5 | GRCh38.p7 | 1:30757629 | TCACACAAGCACGCA[C/T]GCACACACACCCGGG | 7805 |
| rs781572257 | snp | G/T | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30747918 | TGCTGTTGGTGATGT[G/T]GGTGACAGTGATGGG | 7805 |
| rs781756477 | in-del | -/A | | | intron-variant, upstream-variant-2KB | LAPTM5, MIR4420 | GRCh38.p7 | 1:30740333 | GAGTGAACAGGAGGG[-/A]AGGGGCGGGGCACTG | 7805 |
| rs781772593 | snp | A/G | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30756723 | TTGCAGCAACCCACC[A/G]CAGCATGTGGATCTA | 7805 |
| rs796195284 | in-del | -/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30738016 | TTCTCTACAAGATCA[-/T]TTTGGCTGACAGGGA | 7805 |
| rs796266647 | snp | C/T | | | downstream-variant-500B | LAPTM5 | GRCh38.p7 | 1:30732248 | GTGTGGGTGTGTAGG[C/T]GGTGGGAGTGAGTGT | 7805 |
| rs796313659 | snp | G/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30734421 | TTTGCCACCACAAGG[G/T]ATGGGCTTCCGGAAA | 7805 |
| rs796436952 | snp | A/C | | | intron-variant, nc-transcript-variant | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30744271 | GCTGTGGCTGACACT[A/C]ACAGGAAACAGCCCT | 7805 |
| rs796482509 | snp | A/T | | | intron-variant | LAPTM5 | GRCh38.p7 | 1:30737200 | TAACATAATCTCAGG[A/T]ACATTTTGATGCCTG | 7805 |
| rs796804735 | snp | C/T | | | upstream-variant-2KB | LAPTM5 | GRCh38.p7 | 1:30759536 | AGGGATGAAACACAC[C/T]GACAGCATGTGGAAT | 7805 |
| rs796856437 | in-del | -/C | | | intron-variant, downstream-variant-500B | LAPTM5, LOC105378620 | GRCh38.p7 | 1:30743775 | ACCCACCATCTGTTT[-/C]CCCCTTGCTGACTGT | 7805 |