SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9441 | snp | C/T | 0.423413 | 0.180077 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661722 | TCCTTAGGCACCAGT[C/T]TTTGTTAAACAAAAC | 9870 |
rs16661 | snp | A/C | 0.46137 | 0.133501 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661613 | AGGATTAGAAAAAAA[A/C]AAAACAAAACAGTAA | 9870 |
rs752857 | snp | C/T | 0.439085 | 0.163545 | intron-variant | AREL1 | GRCh38.p7 | 14:74664241 | GAATTTACACTGTCA[C/T]ATGATTAGGAGGGTA | 9870 |
rs1045430 | snp | A/C | 0.449726 | 0.150364 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663532 | TCCCTGCCCATATCT[A/C]CCACAGGCCACTTTG | 9870 |
rs1045436 | snp | C/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662114 | GTCCGGGATCCAGCA[C/T]CAGGGTCTCTATACC | 9870 |
rs1045437 | snp | G/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662111 | CGGGATCCAGCATCA[G/T]GGTCTCTATACCCCA | 9870 |
rs1045578 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661442 | GGGCCAGCTACCCTT[C/T]TGGCCTTTTAGCGTC | 9870 |
rs1045621 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661375 | AGTGTCAGCATGTTT[C/T]TGGAAAATTGGCAGA | 9870 |
rs2080669 | snp | A/G | 1.67508e-05 | 0.00289398 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669627 | AGAACATAGGACCCA[A/G]AGGCTTTGTCCTCTT | 9870 |
rs2270424 | snp | A/G | 0.397744 | 0.201673 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692304 | GTGCAGGGTGCAATC[A/G]ACTGCCAAAGGACGC | 9870 |
rs2270425 | snp | C/G | 0.481084 | 0.0953954 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713031 | CCACTCTCCCACCAA[C/G]AGACCCCAGAGTTGG | 9870 |
rs2287399 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | AREL1 | GRCh38.p7 | 14:74670297 | GTAATTCAAAGTGAC[C/T]AGAAGATAAAGGGCA | 9870 |
rs2302832 | snp | C/T | 0.450357 | 0.149522 | intron-variant | AREL1 | GRCh38.p7 | 14:74670961 | TTTATACTCTCCACA[C/T]TCCCTCTATTGTACT | 9870 |
rs2359142 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74689592 | TCTTATAGCACTTTT[C/T]TTTTTTTTTTTTTTT | 9870 |
rs2359143 | snp | A/G | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74701982 | ccaggtcacgctgac[A/G]caagaggtgggttcc | 9870 |
rs2884642 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664449 | TCTTCTTTTCCtttc[C/T]ttttttttttttttt | 9870 |
rs3080652 | in-del | -/TAAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694199 | aaataaataaataaa[-/TAAA]taatGCCAACAGACT | 9870 |
rs3214407 | in-del | -/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713640 | ATTATTTTGTTTTTT[-/T]GCTTATTATCGTGTC | 9870 |
rs3759742 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | AREL1 | GRCh38.p7 | 14:74709121 | CTTTAGCTATTAACT[A/G]ACTTGGGTTTAAATT | 9870 |
rs3813557 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662286 | AGGACTTTGGCAATG[C/G]CTTGGCCTCCTGGAA | 9870 |
rs3813559 | snp | G/T | 0.0240643 | 0.107019 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661716 | GGCACCAGTCTTTGT[G/T]AAACAAAACCCTTTG | 9870 |
rs3834533 | in-del | -/C | 0.0287284 | 0.116357 | intron-variant | AREL1 | GRCh38.p7 | 14:74708662 | GCCAATAGTTAACAT[-/C]TGTTAATTGATTTTC | 9870 |
rs4899529 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74689215 | GTTCTGTAAGCATTT[C/T]CTGTAAGCATGTTCC | 9870 |
rs4899530 | snp | A/G | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74699122 | tactgaatgatctta[A/G]acaagttacagcagg | 9870 |
rs4899531 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74699378 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 9870 |
rs4899532 | snp | A/G | 0.375797 | 0.216044 | intron-variant | AREL1 | GRCh38.p7 | 14:74707429 | gcactttgggaggcc[A/G]aggtgggcggattac | 9870 |
rs5809676 | in-del | -/A | 0.375 | 0.216506 | intron-variant | AREL1 | GRCh38.p7 | 14:74690285 | AAAAAAAAAAAAAAA[-/A]GCTCCAAAGAAACCA | 9870 |
rs6574189 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74699790 | aggacttgctgTAAA[C/T]TTCTCTTCAGTTGCC | 9870 |
rs6574190 | snp | A/G | 0.397271 | 0.202018 | intron-variant | AREL1 | GRCh38.p7 | 14:74700312 | ACAGAAAGCTAAAAT[A/G]ACTTGCCTATAGCCA | 9870 |
rs7143215 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74683987 | TAATGCTACAGTGGA[A/G]AAGTCAATGcaggag | 9870 |
rs7144650 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | AREL1 | GRCh38.p7 | 14:74708403 | TTTGCACAGCCCACC[C/T]GGGATTTCTTCTTTA | 9870 |
rs7145575 | snp | A/T | 0.444133 | 0.157519 | intron-variant | AREL1 | GRCh38.p7 | 14:74678825 | agaacatcttcagga[A/T]ctgagaccaaagatt | 9870 |
rs7148840 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AREL1 | GRCh38.p7 | 14:74684784 | AAAGGAGGTCAGGAT[A/G]AGACTGTAAGACTGC | 9870 |
rs7149057 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74691647 | ACTTGCTTACGAAGG[A/T]TCCTGGTCTGGTTGC | 9870 |
rs7152804 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74697305 | AAAGAAAGACGTTTG[C/T]TTTGTAAGATGCAAT | 9870 |
rs7153812 | snp | A/G | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74706787 | CGTAGTTATACTTCC[A/G]TGTAGTAAAATCTAT | 9870 |
rs7155338 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AREL1 | GRCh38.p7 | 14:74701812 | gttactttctagata[C/T]aatgggagtacaggc | 9870 |
rs7156373 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703431 | caatgggaattatgg[A/G]agctaaaattcaagg | 9870 |
rs7157439 | snp | A/G | 0.0599851 | 0.162463 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711231 | agcgaaactaactcc[A/G]tctcaaaaaaaaaaa | 9870 |
rs7160996 | snp | C/T | 0.459118 | 0.137002 | intron-variant | AREL1 | GRCh38.p7 | 14:74695281 | ggcagggtttcacca[C/T]gttggccaggctggt | 9870 |
rs7493409 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74670335 | ACATAATTAAGAATC[A/T]TATATTAAGTTTGTG | 9870 |
rs8004430 | snp | C/T | 0.393987 | 0.204372 | intron-variant | AREL1 | GRCh38.p7 | 14:74704980 | TTAAGTTTTATTCCC[C/T]TTGTTTCTTTCAAAT | 9870 |
rs8004432 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74704290 | ccaaggttgaagaca[C/T]acgcccaggacacgg | 9870 |
rs8005525 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | AREL1 | GRCh38.p7 | 14:74699687 | acttaattcttgttt[A/C]tatcaattagcctat | 9870 |
rs8005569 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74704927 | ATTTTTTAACAAGAA[C/T]TTTTTAAAACTCCTG | 9870 |
rs8007113 | snp | A/T | 0.41141 | 0.19091 | intron-variant | AREL1 | GRCh38.p7 | 14:74678953 | TGGAGTGTAGTGGCA[A/T]GATCACAGCTCACTG | 9870 |
rs8007335 | snp | A/C | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74687396 | AACTGTGTGACCTAT[A/C]TAGGCTTCAGAATCT | 9870 |
rs8007734 | snp | A/G | 0.141258 | 0.225111 | intron-variant | AREL1 | GRCh38.p7 | 14:74687754 | agttctcaaagtttt[A/G]atgattattACAATT | 9870 |
rs8016694 | snp | C/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662880 | GTCAGTGGCCCAAGC[C/T]GGCCATACTTCAGTG | 9870 |
rs8017229 | snp | C/T | 0.404035 | 0.196909 | intron-variant | AREL1 | GRCh38.p7 | 14:74676897 | TGCCTTCCGGGCTCA[C/T]GCCATTCTCCTGCCT | 9870 |
rs8018237 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | AREL1 | GRCh38.p7 | 14:74672252 | AGGCCAGTAAGTAAA[A/C]TGCTCTTCCCTCGAT | 9870 |
rs8019690 | snp | A/T | 0.416545 | 0.186448 | intron-variant | AREL1 | GRCh38.p7 | 14:74668439 | CTAAAAATGTAAAAC[A/T]TTTTTTCTGTTGGTA | 9870 |
rs9323600 | snp | G/T | 0.443464 | 0.15834 | intron-variant | AREL1 | GRCh38.p7 | 14:74676990 | ATTTTTAGTGGAGAC[G/T]GGGTTTCACTGTGTT | 9870 |
rs9671386 | snp | A/G | 0.39121 | 0.2063 | intron-variant | AREL1 | GRCh38.p7 | 14:74684344 | TCACTAGTTCCTGGA[A/G]GGAGTTGAAAAACAA | 9870 |
rs10133086 | snp | A/G | 0.374 | 0.217081 | intron-variant | AREL1 | GRCh38.p7 | 14:74691264 | GGTCAAGGCTGCAGT[A/G]AGCCATGATTGTGCT | 9870 |
rs10136897 | snp | G/T | 0.372391 | 0.217992 | intron-variant | AREL1 | GRCh38.p7 | 14:74706689 | CAATATGTTGGACCC[G/T]AAAGATTCCAGAATG | 9870 |
rs10137269 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AREL1 | GRCh38.p7 | 14:74677000 | gagacggggtttcac[C/T]gtgttagccaggata | 9870 |
rs10137800 | snp | C/T | 0.372189 | 0.218105 | intron-variant | AREL1 | GRCh38.p7 | 14:74703583 | tacATTTGTATCAca[C/T]gcaaaatgtagtcct | 9870 |
rs10138739 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AREL1 | GRCh38.p7 | 14:74698614 | CCATGGGAGAAGGAC[A/G]ATGCAATGTTGCAAG | 9870 |
rs10145366 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | AREL1 | GRCh38.p7 | 14:74700505 | AAATTTTagccgggc[A/G]cagtggctcacacct | 9870 |
rs10151249 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | AREL1 | GRCh38.p7 | 14:74677693 | tttttagtagagaca[A/G]cgtttcaccatattg | 9870 |
rs10151838 | snp | A/G | 0.279991 | 0.248195 | intron-variant | AREL1 | GRCh38.p7 | 14:74665452 | TTTTTAAATGAAACA[A/G]AGGACAAAACACACA | 9870 |
rs10162454 | snp | C/T | 0.396909 | 0.202282 | intron-variant | AREL1 | GRCh38.p7 | 14:74677915 | ACTGCAAACCCTAAG[C/T]AAAATGAAAAAAACT | 9870 |
rs10220473 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74668300 | CTTAAAACCATCATC[A/C]AGGAATATTTGTGTA | 9870 |
rs10438165 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74715051 | AGTAAGTCTAGCACA[A/T]CTATGTAGATGAAAG | 9870 |
rs10873272 | snp | C/T | 0.388021 | 0.208447 | intron-variant | AREL1 | GRCh38.p7 | 14:74679797 | tgtgccattgcactc[C/T]agcttgggcgtcaga | 9870 |
rs11407786 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691324 | ACCCTGTCTCCATTT[-/A]AAAAAAAAAAAAAAA | 9870 |
rs11537957 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662962 | CCTAGGCATGCCCCA[C/T]TCTGGAGGCTACAGC | 9870 |
rs11537958 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661736 | AGACTGGTGCCTAAG[A/G]ACCACCACAGGGATG | 9870 |
rs11621536 | snp | A/T | 0.00472811 | 0.0483911 | intron-variant | AREL1 | GRCh38.p7 | 14:74669848 | CTGCTTAGAACCACT[A/T]ATCCCTTCAACCTTA | 9870 |
rs11624308 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695190 | gttcaagcgattctc[G/T]tgcctcagcctccct | 9870 |
rs11627017 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693896 | AAATACAGCAACATg[A/G]ccgggcacagtagtt | 9870 |
rs11629369 | snp | A/G | 0.450609 | 0.149185 | intron-variant | AREL1 | GRCh38.p7 | 14:74695318 | CTCCTGACCACAGGT[A/G]ATTCGCCCGCCTCAG | 9870 |
rs11629377 | snp | C/G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665379 | cggcctcctgagtag[C/G/T]tgggattacaggcgA | 9870 |
rs11844127 | snp | C/G | 0.402406 | 0.198172 | intron-variant | AREL1 | GRCh38.p7 | 14:74673233 | ACTGGTAAAGAAAAA[C/G]AAAGAAATTAATCTA | 9870 |
rs12323361 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74705003 | TTTCAAATTCAATGC[C/T]GCACATTACCATGCA | 9870 |
rs12323528 | snp | G/T | 0.440884 | 0.161442 | intron-variant | AREL1 | GRCh38.p7 | 14:74685365 | TACTCCTTGAAGGCA[G/T]ATTTTTGTCTTATTC | 9870 |
rs12323883 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | AREL1 | GRCh38.p7 | 14:74680339 | tttaagaaatgcaaa[C/T]taaaagcacaatgag | 9870 |
rs12433518 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713391 | TCTGGGTTATTTGAG[C/G]CAAGAAGGGAAGGCA | 9870 |
rs12434646 | snp | C/T | 0.44546 | 0.155869 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711990 | TATGACAGAGGTACC[C/T]ATTCCGTTCCCAGCT | 9870 |
rs12434824 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699383 | tgtgtgtgtgagaga[C/G]agagagagagagcaa | 9870 |
rs12587457 | snp | C/T | 0.461259 | 0.133677 | intron-variant | AREL1 | GRCh38.p7 | 14:74697438 | TAACTAAGGAGGTTC[C/T]AAGAATATATCAGAC | 9870 |
rs12589339 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74705627 | CCTTACTGAGTCACT[C/T]TAACCTGTGATGAGA | 9870 |
rs12879930 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699388 | gtgtgagagagagag[A/C]gagagagcaagagca | 9870 |
rs12879939 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699403 | agagagagcaagagc[A/G]agagagagagagaga | 9870 |
rs12883800 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696944 | actccatcctgggtg[A/C]caaagcaagacttcg | 9870 |
rs12883923 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696936 | gccactgcactccat[C/T]ctgggtgacaaagca | 9870 |
rs12883924 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696984 | ataaaataaaataat[A/G]aaataaaataaatta | 9870 |
rs12883928 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696945 | ctccatcctgggtga[A/C]aaagcaagacttcgt | 9870 |
rs12883931 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696990 | taaaataataaaata[A/G]aataaattagctggg | 9870 |
rs12884249 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697123 | ccactgtactctagc[C/T]tgggtaacagagaga | 9870 |
rs12889955 | snp | A/G | 0.44858 | 0.151875 | intron-variant | AREL1 | GRCh38.p7 | 14:74706296 | TATTCCATTAACTGC[A/G]CCTGAAGTGGCAGGC | 9870 |
rs12892795 | snp | A/G | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74664645 | tttgtattgttagta[A/G]agtcgggctttcacc | 9870 |
rs12892937 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74702224 | aaccccacatttccc[C/T]ccaacattgccctag | 9870 |
rs12893245 | snp | A/G | 0.372189 | 0.218105 | intron-variant | AREL1 | GRCh38.p7 | 14:74702233 | tttccccccaacatt[A/G]ccctagcagaggttc | 9870 |
rs12893742 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664639 | tttttttttgtattg[G/T]tagtagagtcgggct | 9870 |
rs12894665 | snp | A/G | 0.3748 | 0.216622 | intron-variant | AREL1 | GRCh38.p7 | 14:74689839 | AACCTGAGGTGATCC[A/G]CCTGCCTCAGCCTCC | 9870 |
rs12896320 | snp | A/G | 0.41023 | 0.191902 | intron-variant | AREL1 | GRCh38.p7 | 14:74677597 | ctgcaacctctgcct[A/G]tcgggttcaagcgat | 9870 |
rs17101802 | snp | A/G | 0.0763149 | 0.179815 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663161 | CCTTAGAGGCAGTCC[A/G]GTGCCATGGCCTATG | 9870 |
rs17101845 | snp | C/T | 0.00783052 | 0.0620802 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670070 | GCCCACGAGCCGTCC[C/T]GCAAACTCATACATT | 9870 |
rs17101852 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | AREL1 | GRCh38.p7 | 14:74671934 | ATGCCACACGGAGAA[C/T]ATGGCTGAGAAAACG | 9870 |
rs17101879 | snp | G/T | 0.221439 | 0.248363 | intron-variant | AREL1 | GRCh38.p7 | 14:74674628 | TAAATAAAAAAAATA[G/T]GACTGACAATGCAGT | 9870 |
rs17101961 | snp | C/T | 0.141934 | 0.225437 | intron-variant | AREL1 | GRCh38.p7 | 14:74686172 | ATGAACTCTGGGTCA[C/T]CCCAATAATAAGCAG | 9870 |
rs17101964 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | AREL1 | GRCh38.p7 | 14:74686901 | ACAGACAATATAAAG[A/G]GCCAAAATTTGGGAT | 9870 |
rs17102009 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | AREL1 | GRCh38.p7 | 14:74693420 | TCTCGAAGATATTCA[G/T]GAACCAAAAATGTAG | 9870 |
rs17102124 | snp | C/T | 0.0139853 | 0.0824443 | intron-variant | AREL1 | GRCh38.p7 | 14:74710723 | TACAGTATCTGTAGC[C/T]ACCATTTCTACATCA | 9870 |
rs17102125 | snp | G/T | 0.155987 | 0.23165 | intron-variant | AREL1 | GRCh38.p7 | 14:74710730 | TCTGTAGCTACCATT[G/T]CTACATCAAAAATTC | 9870 |
rs17102128 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | AREL1 | GRCh38.p7 | 14:74710874 | TGAGCATCCCAGGAC[A/C]TGAAAACTTAATGTT | 9870 |
rs17183132 | snp | A/C | 0.372391 | 0.217992 | intron-variant | AREL1 | GRCh38.p7 | 14:74687115 | TAGGTACTTCCTCAG[A/C]GGGATGCCATTCGAT | 9870 |
rs17183139 | snp | A/G | 0.374 | 0.217081 | intron-variant | AREL1 | GRCh38.p7 | 14:74687247 | AGGAATAAAAGCAGT[A/G]CCAAATGTATGGCTT | 9870 |
rs17782671 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AREL1 | GRCh38.p7 | 14:74670560 | TCAAATATTCAGCTG[C/T]CTGCATTTTTGCTTA | 9870 |
rs17782683 | snp | A/G | 0.444799 | 0.156695 | intron-variant | AREL1 | GRCh38.p7 | 14:74701003 | ATGGAGTAGCTATAC[A/G]CTGGCCACAATATAG | 9870 |
rs17782707 | snp | A/T | 0.372391 | 0.217992 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712399 | TGGCTTTCCACAAAC[A/T]TTCAAGAAATAAGTT | 9870 |
rs17853115 | snp | A/G/T | 3.31587e-05 | 0.00407164 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670807 | GAAGAGCTGATTGGT[A/G/T]GTATCAAATAGTGCT | 9870 |
rs17853116 | snp | G/T | | | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674074 | GTGTAAAGGCGCCAG[G/T]GGATGATCTTCAGGT | 9870 |
rs17853117 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683436 | TGAAGGACTTCCTGG[G/T]TCACTGGAATTTCCA | 9870 |
rs17853118 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684676 | CACAGACACTGTGAT[C/T]CCACCTATGCAAAAG | 9870 |
rs28464554 | snp | A/C | 0.372391 | 0.217992 | intron-variant | AREL1 | GRCh38.p7 | 14:74707891 | GAACCCGGGAGGCGG[A/C]GCTTGCAGTGAGCCG | 9870 |
rs28565226 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696874 | GAGACTGAGGCAGGA[C/G]AATCACTTGAACTTG | 9870 |
rs28578498 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74708664 | AAATCAATTAACAGA[A/T]GTTAACTATTGGCAT | 9870 |
rs34192596 | in-del | -/AA | 0.465788 | 0.126237 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661606 | TGAAAGCAGGATTAG[-/AA]AAAAAAAAAACAAAA | 9870 |
rs34261059 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680921 | ACATAGTGGCTCATG[-/C]CCTGTAATCCCAGCA | 9870 |
rs34300637 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679848 | AAAGAAAATAATAAT[-/A]AATAAATAAATAAAT | 9870 |
rs34302121 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709746 | TATCATGTAAGTCAG[-/A]AAAATAAATGTAAAA | 9870 |
rs34340758 | in-del | -/TT | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74671344 | GGAGGTAAGAGTTGC[-/TT]TTTTTTTTTTTTTTT | 9870 |
rs34372609 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679720 | TAATCCCAGCTACTT[-/G]GGGAGGCTGAGGCAG | 9870 |
rs34372758 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678470 | CCACTGCACTCAGCC[-/T]TGGGTGACAGAGTGA | 9870 |
rs34442026 | in-del | -/A | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662480 | AATCAAACAGTAATG[-/A]AAAAGGATGTTGTCA | 9870 |
rs34514467 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699240 | GAGTTCACACATTCT[-/G]CTGTGTGGGTTTTCT | 9870 |
rs34523027 | snp | A/T | 0.000364444 | 0.013494 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676614 | GTGTAATTGTGCTCA[A/T]CTCTCAAGGACATGG | 9870 |
rs34581505 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685366 | CTCCTTGAAGGCAGA[-/T]TTTTTGTCTTATTCA | 9870 |
rs34713411 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708911 | AAAAGAGCCACCAGG[-/A]AAAACATCACTATGG | 9870 |
rs34834243 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686165 | ATTAAAATGAACTCT[-/G]GGGTCATCCCAATAA | 9870 |
rs34976163 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | AREL1 | GRCh38.p7 | 14:74698792 | ACTTTGGGAGGCTGA[A/G]GTGGGAGGATGGCTT | 9870 |
rs35110207 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685398 | TTTAGACTCCACAGT[-/A]AAACAGTGTCTGGCA | 9870 |
rs35148185 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692151 | CACATGAAAGAAAAA[-/C]CGCCACAAGGTCAAC | 9870 |
rs35181427 | in-del | -/A | 0.489024 | 0.0732638 | intron-variant | AREL1 | GRCh38.p7 | 14:74707792 | AGTGAGATTCGTCTC[-/A]AAAAAAAAAAAAAAA | 9870 |
rs35296214 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683586 | AGGAAAAAAACATTT[-/T]CCTGTGTAGAGTGAG | 9870 |
rs35356315 | in-del | -/A | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714598 | TGAGAGATTCTGACT[-/A]AAAAATAAATATAGT | 9870 |
rs35400612 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668841 | AGAAGCACATGCATC[-/G]GGAAATATCTCTGGG | 9870 |
rs35537432 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709720 | AATGTTTGTTGGGAG[-/A]AAAAAAGTCCTATCA | 9870 |
rs35591392 | snp | G/T | 0.452719 | 0.146304 | intron-variant | AREL1 | GRCh38.p7 | 14:74691010 | GTAAGTGACAGAGTT[G/T]AGATTCAAGCCGGGC | 9870 |
rs35606546 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674919 | TATGTTGGTGGTATA[-/G]GGGGAAGGTCCTCAC | 9870 |
rs35652312 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712834 | CTACTGGGCAAACCA[-/G]GGAGTCTGAACCCCC | 9870 |
rs35713526 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709222 | GGGAGGATGGCTTGA[-/G]GGCCAGGAGTTCAAG | 9870 |
rs35768674 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710915 | GAACACGTTCAAGTT[-/T]CCAGTGCAACTATGT | 9870 |
rs35803151 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | AREL1 | GRCh38.p7 | 14:74677585 | GATCTCGGCTCACTG[C/T]AACCTCTGCCTATCG | 9870 |
rs35842570 | in-del | -/A | | | upstream-variant-2KB, frameshift-variant, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714897 | GATAGATTAAAACCT[-/A]AAAAGAAAGAAAAGA | 9870 |
rs35864766 | snp | A/G | 0.0297486 | 0.118276 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675903 | AAAGTAAATGCTCAC[A/G]CCTGAAGTGGACACA | 9870 |
rs35874855 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665386 | TGAGTAGCTGGGATT[-/C]ACAGGCGAGGTATTT | 9870 |
rs35892587 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692377 | AGGTTTTTATTTCTG[-/A]AAAGGATTCCCCAGA | 9870 |
rs35901005 | in-del | -/A | 0.499767 | 0.0107802 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714779 | TTTCTTCAGTAGACC[-/A]AAAAAAAAAAAAAAT | 9870 |
rs35945510 | snp | C/T | 0.00034776 | 0.0131818 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672910 | ACCTGCCGAAGCTCT[C/T]GCTGGAAAAAGTTCA | 9870 |
rs35986988 | in-del | -/A | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74691348 | AAAAAAAAAAAAAAA[-/A]GCCTACGTCTAACTC | 9870 |
rs36052941 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677564 | CAAGCTGGAATGCAG[G/T]GGCACGATCTCGGCT | 9870 |
rs45559240 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74685758 | CGTGAGCCAAACAAC[C/T]CTCTCTAGTCCAGAG | 9870 |
rs45569736 | snp | A/C/T | 0.0072114 | 0.0596137 | intron-variant | AREL1 | GRCh38.p7 | 14:74684419 | CAAGTTACTCAGAAA[A/C/T]CCCAATGGGTATGGA | 9870 |
rs55638691 | snp | C/G | 0.450734 | 0.149016 | intron-variant | AREL1 | GRCh38.p7 | 14:74699385 | TGTGTGTGAGAGAGA[C/G]AGAGAGAGAGCAAGA | 9870 |
rs56253619 | snp | C/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74666083 | AGAGTTCATTTTGTT[C/T]GGATTTCACATCTGA | 9870 |
rs56728679 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664471 | TTTTTTTTTTTTTTT[-/T]GAGAAAGAGTCTCGC | 9870 |
rs57270744 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694350 | AGGAATTTTTAAATG[A/C]CACTTTTAAGGAATA | 9870 |
rs57373009 | in-del | -/AG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699394 | GAGAGAGAGAGAGAG[-/AG]CAAGAGCAAGAGAGA | 9870 |
rs57414095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74691087 | ACTTTGGAAGCCAAG[A/G]CAGGAGGATCACTTG | 9870 |
rs57614901 | snp | A/T | 0.35445 | 0.227135 | intron-variant | AREL1 | GRCh38.p7 | 14:74699380 | GTGTGTGTGTGTGAG[A/T]GAGAGAGAGAGAGAG | 9870 |
rs57846981 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664280 | CTGTTGGTTCTCTTT[C/T]TTCGCCATCTCCAAT | 9870 |
rs58148649 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684108 | GTGAAAACAGCCATA[A/G]TCAATACATGATGAA | 9870 |
rs58161849 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705044 | TGTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCGC | 9870 |
rs58383006 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677524 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCACGC | 9870 |
rs59222572 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | AREL1 | GRCh38.p7 | 14:74694764 | GGAGGCTGAAGCGGG[A/C]GGATCATGAGGTCAG | 9870 |
rs59741016 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | AREL1 | GRCh38.p7 | 14:74692772 | GCAGTGGCATGATTA[C/T]AGCTCACTGCAGCCT | 9870 |
rs60032703 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664632 | TTTTTTTTTTTTTTT[-/T]GTATTGTTAGTAGAG | 9870 |
rs61412932 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671454 | CTTGCTCCAATCTGA[A/G]ATGGAGAAATTCCGA | 9870 |
rs61532288 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | AREL1 | GRCh38.p7 | 14:74706971 | AGTATTACTTATTCT[A/C]AGGGTCAATGACTCT | 9870 |
rs61569648 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690261 | AGAGCAAGACCCTGT[C/T]TCCAAAAAAAAAAAA | 9870 |
rs61978883 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74687867 | CAAAGAGAAATGCAT[C/G]TGAATTTCAAAAGGC | 9870 |
rs61978885 | snp | A/G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694921 | GTGAACCCGGGAGGC[A/G/T]GAGTTTGCCGTGAGC | 9870 |
rs61978886 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74696499 | CCGGGTTGCTAAAAT[G/T]ACTATAACACATACT | 9870 |
rs61978899 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714622 | ATATAGTATAATCAG[A/C]TTTTATTTACTCATT | 9870 |
rs71119311 | in-del | -/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74678715 | TGGGTCAAGGTCCTC[-/T]TTTTTTTTTTTTTTT | 9870 |
rs71119314 | in-del | -/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74707807 | ACCATACCCGTCTAA[-/T]TTTTTTTTTTTTTTT | 9870 |
rs71426990 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74696969 | ACTTCGTCTCAAAAA[A/T]TGAAATAAAATAATG | 9870 |
rs71429057 | snp | A/C | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74691153 | CAAAACCCTGTCTCT[A/C]CAAAAAATACAAAGA | 9870 |
rs71449202 | in-del | -/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74666737 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTAC | 9870 |
rs72732166 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74670992 | ACTCTGGTGTTTCTC[C/G]GTTGCGACTCATCTA | 9870 |
rs72732168 | snp | C/T | 0.021333 | 0.101051 | intron-variant | AREL1 | GRCh38.p7 | 14:74682483 | CAATTCGACCACCAA[C/T]TGATGAAAGGATAAA | 9870 |
rs72732169 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74697729 | GATCTGGTAATGAGG[C/T]GCCTCCAAATGACTG | 9870 |
rs73301903 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662230 | CAGCTCAGGAGGGCT[C/T]GTTCCTCATGATCCC | 9870 |
rs73301904 | snp | A/G | 0.0364509 | 0.129988 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662671 | CCCTAGTGTCCTGAC[A/G]CCAAGGACCTGTGAT | 9870 |
rs73301905 | snp | C/T | 0.00195393 | 0.0311953 | intron-variant | AREL1 | GRCh38.p7 | 14:74672822 | TGACAGAGATGAAAT[C/T]TTACCTACCGATTCC | 9870 |
rs73301907 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | AREL1 | GRCh38.p7 | 14:74673414 | AATTATTTTAGTCAC[A/C]GAGACTGCCTTTAGT | 9870 |
rs73301909 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AREL1 | GRCh38.p7 | 14:74673478 | ATAAAATATAAGAAG[A/G]GTGATATGTTAAATA | 9870 |
rs73301911 | snp | A/T | 0.0368353 | 0.130617 | intron-variant | AREL1 | GRCh38.p7 | 14:74674617 | AAAAAATAAAATAAA[A/T]AAAAAAAATATGACT | 9870 |
rs73301914 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | AREL1 | GRCh38.p7 | 14:74681248 | CAAAACCACACATCT[C/G]GTCCCAAGCATTTTG | 9870 |
rs73301915 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | AREL1 | GRCh38.p7 | 14:74682436 | ACACAAATGTTCACA[A/G]TAGTGTTGCTTACAG | 9870 |
rs73301919 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74686781 | GTCAAAAGTTTCATA[A/C]AAATCCTACTTAGAG | 9870 |
rs73301921 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AREL1 | GRCh38.p7 | 14:74690112 | ACAAATTAGCTGGGC[A/G]TGCTGGCACACACCT | 9870 |
rs73301930 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | AREL1 | GRCh38.p7 | 14:74708502 | TATATACCGGGGGTA[C/T]CTTGAATTTGAACTT | 9870 |
rs73301933 | snp | A/G | 0.00225434 | 0.0334976 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713155 | TGACGTAGAAGTATT[A/G]CGCCGTTGGTGATTA | 9870 |
rs74248174 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712086 | AAAAAAAGAAAGAAA[A/G]AAAGAAAGAAAAAGA | 9870 |
rs74328362 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AREL1 | GRCh38.p7 | 14:74685765 | CAAACAACTCTCTCT[A/G]GTCCAGAGCCTTACT | 9870 |
rs74354930 | snp | G/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74665288 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT | 9870 |
rs74357502 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74665983 | TGCTTCAAAATGTAA[C/T]AAAATTTACCAGTAG | 9870 |
rs74444150 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AREL1 | GRCh38.p7 | 14:74688680 | CAAAATGTCCCACTG[C/T]TCTACAACAGCTCTC | 9870 |
rs74468206 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711792 | AGATAGATTAACTCA[C/T]CCAATGTCATGGCGA | 9870 |
rs74553577 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AREL1 | GRCh38.p7 | 14:74700148 | GTTCTCTGAAGGATG[A/G]TGATAACAAGAATCA | 9870 |
rs74690289 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | AREL1 | GRCh38.p7 | 14:74665430 | TAAGAACTGCTACTA[C/T]GGATTATTTTTAAAT | 9870 |
rs74694089 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | AREL1 | GRCh38.p7 | 14:74698414 | GGAGGCATGAAATGG[G/T]GTTACAGTCTAATTC | 9870 |
rs74703768 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74664615 | CCACACCCAGCTAAT[A/T]TTTTTTTTTTTTTTT | 9870 |
rs74718095 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | AREL1 | GRCh38.p7 | 14:74675409 | AAATTCACCTTCTTT[C/T]CTCTGCCAAAATTTC | 9870 |
rs74752190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680428 | TAGCAAGGATGTGAA[C/G]AAACTGGATTATTCA | 9870 |
rs74932001 | snp | C/T | 0.0240643 | 0.107019 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661576 | TATTGTACCTTTTCC[C/T]CACACTGGCTAGTAT | 9870 |
rs74947053 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | AREL1 | GRCh38.p7 | 14:74693475 | ATACACAAACAGCCA[C/T]CATAAGACAAATGAG | 9870 |
rs74959318 | snp | A/C | 0.00597247 | 0.0543191 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662356 | ATAAAGATGGCTTGT[A/C]ATATTCTCAGAGTTG | 9870 |
rs74965221 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692044 | CTGTTACCTTACCTT[A/T]AAACGAGGGCCCATG | 9870 |
rs75046505 | snp | A/C | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74678698 | GACATGTATAAGCAA[A/C]AAAAAAAAAAAAAAA | 9870 |
rs75121602 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | AREL1 | GRCh38.p7 | 14:74687643 | TTAATCTTTGTAAAG[A/G]AGTGCCAGTTTCCTT | 9870 |
rs75122083 | snp | A/C | 0.0248432 | 0.108648 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714398 | ATTTTTAGGAATGAC[A/C]CTCCATTAATAATAA | 9870 |
rs75140279 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AREL1 | GRCh38.p7 | 14:74704539 | CTATCTCGGTAGGCA[A/G]GGGATGACTCTGAAC | 9870 |
rs75193965 | snp | G/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74671346 | TTTTTTTTTTTTTTT[G/T]TGGAGAAGGTGCGAG | 9870 |
rs75417895 | snp | C/G | 0.0333238 | 0.124705 | intron-variant | AREL1 | GRCh38.p7 | 14:74698717 | GCAGAGACAACAGAG[C/G]TGATTACTTAAGAAT | 9870 |
rs75525848 | snp | G/T | 0.0752113 | 0.178743 | intron-variant | AREL1 | GRCh38.p7 | 14:74675570 | TAACAGTTGAAAGTG[G/T]CTTTCTATACAACTA | 9870 |
rs75583572 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74694305 | CTATATACGTAAGCT[A/G]TAAGAGAGCACTATG | 9870 |
rs75770584 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707977 | AAAAAAAAAAAAAAA[A/G]AAATTACACATGATC | 9870 |
rs75801078 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | AREL1 | GRCh38.p7 | 14:74675090 | GACAAAGAAGTATAA[C/T]GAAACTATCAGCTGC | 9870 |
rs75844788 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690748 | TCTTTAGTGTCCTTG[A/T]CCTTTATAAATATGG | 9870 |
rs75868746 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | AREL1 | GRCh38.p7 | 14:74690310 | AAACCAACATAATTG[C/T]ATATAGTAACTTCAA | 9870 |
rs75962251 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663656 | GATCAGTGGTTATGA[C/T]GTCTGTAACTTGCGC | 9870 |
rs76067794 | snp | A/G | 0.00489019 | 0.0492055 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683458 | GAATTTCCACTGCTA[A/G]CTCGACATGAGAGAT | 9870 |
rs76119092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74670220 | CCCATGCCAAAGGAA[C/T]AAGATGTCACTGTGA | 9870 |
rs76131377 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74705989 | GTAACCTCATGGGGA[C/G]AAAAACAAAAGAGAA | 9870 |
rs76235211 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | AREL1 | GRCh38.p7 | 14:74680450 | GATTATTCATACATT[A/G]CTGGTGGGAATGTAA | 9870 |
rs76310139 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AREL1 | GRCh38.p7 | 14:74685446 | ATAAACCCAAATGAA[C/T]GAATTCCAATGCCAA | 9870 |
rs76670721 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74698678 | GCAGAGGAAGGAGAA[G/T]TAACTGTATGTGCAA | 9870 |
rs77043880 | snp | C/T | 0.00359567 | 0.0422482 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670102 | TCAGGCGCAGATGAG[C/T]GGGGCGATTAGGGTT | 9870 |
rs77280012 | snp | A/C | 0.031825 | 0.122064 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663235 | TCTGTCCCCCTCTCT[A/C]CTGGCTCCTGATGAG | 9870 |
rs77287217 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74692600 | CAGAGCTTCCTTCAG[G/T]TCACTGTCCCCAAAT | 9870 |
rs77297305 | snp | A/C | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74707792 | GAGTGAGATTCGTCT[A/C]AAAAAAAAAAAAAAA | 9870 |
rs77357597 | snp | A/C | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74707795 | TGAGATTCGTCTCAA[A/C]AAAAAAAAAAAATTA | 9870 |
rs77675957 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | AREL1 | GRCh38.p7 | 14:74691320 | GAAAGACCCTGTCTC[C/T]ATTTAAAAAAAAAAA | 9870 |
rs77862665 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74665808 | AAAGAATAATACATT[C/T]TAACCAGAGACAAGA | 9870 |
rs78031907 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74687018 | TCAAAAATCTGCTAC[C/G]ATCTCTCAAAAAGCA | 9870 |
rs78051718 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | AREL1 | GRCh38.p7 | 14:74699521 | TCAACCGTGGACTGG[A/G]ATAATTGGGTAAATG | 9870 |
rs78267589 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | AREL1 | GRCh38.p7 | 14:74706626 | TTTTACCAAAGAAAG[A/G]TCTATTAATTTCTTC | 9870 |
rs78316712 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | AREL1 | GRCh38.p7 | 14:74697873 | CCGTATTAGACTGTA[C/T]CTCATTCTATAACTC | 9870 |
rs78333727 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | AREL1 | GRCh38.p7 | 14:74668876 | CATTTTCTAATAAAA[A/G]GTTTTGGTTTTATTA | 9870 |
rs78399573 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669473 | GCCAAGTGTAGTTAT[A/C/G]TAAGTATACATTAAC | 9870 |
rs78780006 | in-del | -/AAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677829 | TATTAAAAAAAAAAA[-/AAA]GAGGAAAAAACAGAA | 9870 |
rs78806505 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74671835 | AAGCTGTAGGCAAAA[A/G]AACCAAGGAATCCTG | 9870 |
rs78890521 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | AREL1 | GRCh38.p7 | 14:74687816 | CTTTACTTCAAAGCT[A/G]ATAGGAAACTCCTCT | 9870 |
rs79070663 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | AREL1 | GRCh38.p7 | 14:74665473 | AAAACACACACACAC[A/G]AACTGTTTCCTGACA | 9870 |
rs79150314 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711975 | ATGCAATAAGAAAAG[C/T]ATGACAGAGGTACCC | 9870 |
rs79197559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680920 | AGACATAGTGGCTCA[G/T]GCCTGTAATCCCAGC | 9870 |
rs79420292 | snp | A/C | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74699489 | TTCCCAACTTGCACC[A/C]TAAGCCCTGGCCACC | 9870 |
rs79591500 | snp | A/G | 0.030278 | 0.119257 | intron-variant | AREL1 | GRCh38.p7 | 14:74708020 | GGTATTCTAGATTCA[A/G]TTTGGGTATAGAAAA | 9870 |
rs80043099 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662212 | GTCAGGCAGGAACTG[C/T]AGCAGCTCAGGAGGG | 9870 |
rs80086627 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | AREL1 | GRCh38.p7 | 14:74681229 | TTTGGAGAGAAAAAA[A/C]CCACAAAACCACACA | 9870 |
rs80194463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697219 | ATTTCAAAATTTTGG[G/T]GCATACAGAGCTAGT | 9870 |
rs80220122 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693721 | ACAACCTGGACCCAG[A/T]ATCCCTGCTTTTAAT | 9870 |
rs80238036 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704399 | CATCAATCAAGATGT[A/G]TACTGGCTCAGTCCA | 9870 |
rs80323667 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74696462 | TTCCTAAAACTAGTA[C/T]CTCGGGGACCAAATA | 9870 |
rs80335637 | in-del | -/TT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689026 | TATTTTTTTTTTTTT[-/TT]AGTAGAGACAGGGTT | 9870 |
rs80343550 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709316 | AGTCCATTAAGGTCA[A/T]AAAATCTGATCTATT | 9870 |
rs111417364 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | AREL1 | GRCh38.p7 | 14:74689844 | GAGGTGATCCGCCTG[C/T]CTCAGCCTCCCAAAG | 9870 |
rs111545934 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712118 | AAAAAGAAATACAAG[C/T]ACAGACTTTGGAATC | 9870 |
rs111717227 | snp | A/G | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74674832 | CAACCCATACACACT[A/G]CTTTATACCTATTTG | 9870 |
rs111759757 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74682614 | GTACCCTCCAAATCG[C/T]ATGTTGAAATGTGAT | 9870 |
rs111779038 | snp | A/G | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74696486 | CCAAATACTGTATCC[A/G]GGTTGCTAAAATTAC | 9870 |
rs111795461 | snp | C/T | 0.5 | 0 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692184 | AAAGGGTCTATCCAT[C/T]AGACTTTGTCACAGT | 9870 |
rs111844385 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74689261 | TCTCTCTGTCCTGTA[A/T]CTACTGCTACCCCTA | 9870 |
rs111888275 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74689825 | GATCTCAAACTCCCA[A/G]CCTGAGGTGATCCGC | 9870 |
rs111971760 | snp | A/G | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74682838 | TCCTGCTCCCGCTTC[A/G]CCTTCCACCATGAGT | 9870 |
rs112030110 | snp | C/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74704292 | AAGGTTGAAGACATA[C/T]GCCCAGGACACGGCC | 9870 |
rs112083260 | snp | A/G | 0.00011591 | 0.00761195 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663937 | GCTATGGGTCGGAGC[A/G]GCAATAATCTGAAAT | 9870 |
rs112288215 | snp | C/T | 0.284209 | 0.247648 | intron-variant | AREL1 | GRCh38.p7 | 14:74688182 | AGGTGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 9870 |
rs112328689 | snp | A/G | 8.2918e-05 | 0.00643833 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684583 | GTCCCCTCGGCGCTC[A/G]CGGTCCTCATTCTGG | 9870 |
rs112381920 | in-del | -/CT | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712865 | CTACCCTTTTCCTCC[-/CT]CTCTCTCTGGAACTC | 9870 |
rs112702281 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74702614 | CCCTGGAGACATTTT[C/G]CCCATTGTCTTGGTG | 9870 |
rs112799223 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | AREL1 | GRCh38.p7 | 14:74695381 | CACCACACCCAGCCT[C/G]AACTTTTATTTCTAT | 9870 |
rs112834498 | in-del | -/A | 0.172028 | 0.23753 | intron-variant | AREL1 | GRCh38.p7 | 14:74678496 | GTGAGACCCTGCCTC[-/A]AAAAAAAAAAAAGAA | 9870 |
rs112910974 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711569 | AAAATAAAATAAAAT[A/G]AAATTGGCATAAAAT | 9870 |
rs112931375 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688032 | TACTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTGA | 9870 |
rs112954165 | snp | A/G | 8.42666e-05 | 0.00649047 | intron-variant | AREL1 | GRCh38.p7 | 14:74673252 | GAAATTAATCTATAA[A/G]ACCCTCAAGGCCAGT | 9870 |
rs112999456 | in-del | -/ACACACAC | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74697156 | GATCCTGTCACACAT[-/ACACACAC]ACACACACACACAGC | 9870 |
rs113016558 | snp | A/G | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74683981 | CAAGCTTAATGCTAC[A/G]GTGGAGAAGTCAATG | 9870 |
rs113093756 | in-del | -/AGTATATCTGTCTTTTATA | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74672359 | AGGTTTCAGAAATTT[-/AGTATATCTGTCTTTTATA]AGTATATCTGTCTTT | 9870 |
rs113125830 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | AREL1 | GRCh38.p7 | 14:74702365 | ACTTCTGTGCACCCA[A/C]AGGCTCAACATCACG | 9870 |
rs113140862 | snp | C/T | 8.29304e-05 | 0.00643882 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670830 | ATAGTGCTTTGCAGA[C/T]TAGCTCAAACCATTC | 9870 |
rs113145644 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713189 | AAGAACCAGGAGTTT[A/G]GCGTGACCATGGTGA | 9870 |
rs113166865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688961 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 9870 |
rs113173712 | snp | C/T | 0 | 0 | intron-variant, splice-acceptor-variant | AREL1 | GRCh38.p7 | 14:74698857 | AGTGAGATCCCATCT[C/T]TAAAAAAAAAAAAAA | 9870 |
rs113183297 | snp | A/G | 0.371177 | 0.218669 | intron-variant | AREL1 | GRCh38.p7 | 14:74694954 | AGATTGCGCCACTGC[A/G]CTCCAGCCTGGGCGA | 9870 |
rs113290657 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74675513 | ATTGTTTTGACACAG[C/T]ACAAGAAGCCAACAG | 9870 |
rs113322549 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665286 | TTTTTTTTTTTTTTT[C/T]TGAGACGGAGTCTCA | 9870 |
rs113375976 | snp | C/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74710829 | AGAAAAAGTTTACAC[C/T]CAAATCAACAGAAGA | 9870 |
rs113469543 | snp | G/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74687374 | GGAGAACAATCCCAG[G/T]ACTGCAAACTGTGTG | 9870 |
rs113560779 | snp | C/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663461 | GGACCAAATAAATGA[C/T]AGCAGCATGGTCCTC | 9870 |
rs113561263 | snp | A/G | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692291 | GGACTTCTCTCTAGT[A/G]CAGGGTGCAATCGAC | 9870 |
rs113608381 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74693246 | TATCAGCCTATGCAG[C/T]CTGCTCCCTTCGTGC | 9870 |
rs113669825 | snp | G/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74665158 | GGCTTTTAAAATATA[G/T]ATTTATACAAGTGTT | 9870 |
rs113695585 | snp | C/T | 8.32106e-05 | 0.00644968 | intron-variant | AREL1 | GRCh38.p7 | 14:74669815 | AGAACATGAATACTC[C/T]TGCCCTGAAAGGTGT | 9870 |
rs113696449 | snp | C/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74698632 | GCAATGTTGCAAGTG[C/T]CATAAAAGAGGAATA | 9870 |
rs113831113 | snp | C/T | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74678261 | CAACACTTTGGAAGG[C/T]CAAAGCAGGAAGATT | 9870 |
rs113886223 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74691192 | GGATGTCATAGTGCA[C/T]GCCTGCAGTCCCAGT | 9870 |
rs113892770 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688031 | TTACTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 9870 |
rs113892944 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74709578 | AATGACCAAGCGGCA[A/G]TAATCTATCTCTGAG | 9870 |
rs114071492 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74666562 | TTCATTAGAATGTAG[C/T]CCATGAGGGCTGGAA | 9870 |
rs114089356 | snp | C/G | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714716 | CACTAGAGTTATTTG[C/G]TCAGAAAGAGTATGC | 9870 |
rs114161660 | snp | C/G | 0.0437281 | 0.141251 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714329 | GAATAAGAGAATAGT[C/G]GTTAAAACCTTCAGA | 9870 |
rs114217044 | snp | A/T | 0.0256215 | 0.110247 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660758 | AAACTTCTTAGGAGC[A/T]GTATTTTTGTTTGCC | 9870 |
rs114370888 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663411 | ACAGGGCTGAGCCCC[A/G]TGTGCCATCTCCCTC | 9870 |
rs114401289 | snp | C/T | 0.00239838 | 0.0345461 | intron-variant | AREL1 | GRCh38.p7 | 14:74663851 | GGAGAAGTGATTAAC[C/T]CATACCACCAAAAAC | 9870 |
rs114570969 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | AREL1 | GRCh38.p7 | 14:74701022 | GCCACAATATAGACA[C/G]GGTCCAACATAGACC | 9870 |
rs114602349 | snp | A/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713428 | AAGAGAAAAGAAGAG[A/T]CTTTAAAAGATGCCG | 9870 |
rs114719078 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AREL1 | GRCh38.p7 | 14:74688774 | ATTTGCCTTCGTTCT[A/G]CAAATTCCCCCTTTC | 9870 |
rs114787957 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74697118 | CCACACCACTGTACT[C/T]TAGCCTGGGTAACAG | 9870 |
rs115131528 | snp | A/G | 0.0256215 | 0.110247 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661008 | CTTCTTCAGAAACTG[A/G]GCATAAACACTTGTC | 9870 |
rs115139249 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | AREL1 | GRCh38.p7 | 14:74698142 | TTGGGCCTCTGCTCC[C/T]GGCACCAAGGAGTTA | 9870 |
rs115224556 | snp | C/G | 0.0119091 | 0.0762411 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661788 | AATGGTGCCTAAGAT[C/G]CTCTGAAAAAGTGCT | 9870 |
rs115302452 | snp | C/T | 0.031825 | 0.122064 | intron-variant | AREL1 | GRCh38.p7 | 14:74672716 | CCCCAGCCTGGGCAA[C/T]AGAGTGAGACCCTAT | 9870 |
rs115323530 | snp | A/G | 0.00487395 | 0.0491245 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672864 | TCTGCTGACCTTCAG[A/G]GTGACTTTGGAATGT | 9870 |
rs115494409 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | AREL1 | GRCh38.p7 | 14:74703712 | TCCATTAAATGGACA[C/T]ACTGCAATCTGTTTA | 9870 |
rs115498311 | snp | A/G | 1.65592e-05 | 0.00287738 | missense | AREL1 | GRCh38.p7 | 14:74663790 | TGCACCTCTTCATAG[A/G]AGTCATATGTAGGGA | 9870 |
rs115536512 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | AREL1 | GRCh38.p7 | 14:74696352 | ACTATGACTTGATGG[C/T]TTTATTCTTCCCATA | 9870 |
rs115688018 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74706854 | CAAGATCAGCTCTTA[A/G]CTTCTCAGGAAAGTT | 9870 |
rs116037900 | snp | A/T | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74696012 | AGTCAGCAAGCCAAA[A/T]CCTAACAGCCGCCTG | 9870 |
rs116056495 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | AREL1 | GRCh38.p7 | 14:74664650 | ATTGTTAGTAGAGTC[C/G]GGCTTTCACCATGTG | 9870 |
rs116234991 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | AREL1 | GRCh38.p7 | 14:74684058 | TTGGCTTTGTGGACC[A/G]TACACAACTACTCAA | 9870 |
rs116296013 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | AREL1 | GRCh38.p7 | 14:74702432 | AGCGATGGCCCAAGC[C/T]GTACCTTGGCTCCTT | 9870 |
rs116394701 | snp | A/G | 0.00698366 | 0.0586776 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712894 | CTCTGGTAAAGGCAG[A/G]TCTTCTGGGCTCTGC | 9870 |
rs116451601 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AREL1 | GRCh38.p7 | 14:74683790 | TTACCACTAAATCAA[A/G]AAAATGTCCATTTTA | 9870 |
rs116607112 | snp | G/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714683 | GTTAATTCTGATACT[G/T]CCAGGTACTGTGCTT | 9870 |
rs116711204 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | AREL1 | GRCh38.p7 | 14:74690934 | TGAATACTATTATTC[A/T]CGTTTTATGGATTTT | 9870 |
rs116712648 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74681756 | GCCTGGCGACAGGGC[A/G]AGACGCCATCAAAAA | 9870 |
rs116878672 | snp | C/T | 0.000201501 | 0.0100354 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669618 | GGAAACTGGAGAACA[C/T]AGGACCCAGAGGCTT | 9870 |
rs116898252 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AREL1 | GRCh38.p7 | 14:74681755 | AGCCTGGCGACAGGG[C/T]GAGACGCCATCAAAA | 9870 |
rs117070072 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | AREL1 | GRCh38.p7 | 14:74694699 | TCAAATAAGAAAATG[A/G]TATAAAGAGGCTGGG | 9870 |
rs117110221 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712587 | TTGGGTAAGTAGTAA[C/T]ATATGCAAGCTTATG | 9870 |
rs117214661 | snp | A/G | 0.0116103 | 0.0753019 | intron-variant | AREL1 | GRCh38.p7 | 14:74684708 | GAGAACACACAAACC[A/G]CCTGCCAGTTACACA | 9870 |
rs117416960 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | AREL1 | GRCh38.p7 | 14:74695546 | TACTGAGCTTCAAAA[C/T]TCAACTCAAGCACTC | 9870 |
rs117525408 | snp | C/T | 0.000132589 | 0.00814105 | intron-variant | AREL1 | GRCh38.p7 | 14:74667389 | AGGCCTGAAACAAAG[C/T]AGGCAAGTTAAAGTC | 9870 |
rs117813953 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | AREL1 | GRCh38.p7 | 14:74709322 | TTAAGGTCATAAAAT[C/T]TGATCTATTACATGG | 9870 |
rs117851364 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74695653 | GTGGTGCTCCTCTGC[C/T]GAAGATACCTCCGTT | 9870 |
rs118188765 | snp | A/G | 0.0202468 | 0.0985569 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685644 | TGCCAACAGACAGCC[A/G]AGGATCACAGCTGCA | 9870 |
rs137859185 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AREL1 | GRCh38.p7 | 14:74704322 | CTCATGAGGTCCTGA[C/T]GACATGTGCCCAAGG | 9870 |
rs137951045 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74675222 | ATGAAGAATGGTACA[C/T]AGCAAAGTGTTCTGA | 9870 |
rs137991501 | in-del | -/AG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699404 | GAGAGAGCAAGAGCA[-/AG]AGAGAGAGAGAGAGA | 9870 |
rs137992972 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712204 | AAATAAAAGAATTTA[A/T]GTTATTGAGAAGGTC | 9870 |
rs138013338 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680640 | CAAATGGAAACAACC[C/T]AGATGACCTTTAACA | 9870 |
rs138028889 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74709048 | TATGAAAGAACATTA[C/G]TGAAGGCTAAGCATT | 9870 |
rs138200336 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684099 | ACTCAGGTGTGAAAA[-/C]CAGCCATAGTCAATA | 9870 |
rs138360752 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712647 | TCAAACACTGCTTCA[C/T]TTCTCTCTTCACCGA | 9870 |
rs138398700 | in-del | -/AAACAAAAACAA | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74672737 | GAGACCCTATCTCCC[-/AAACAAAAACAA]AAACAAAAACAGTAA | 9870 |
rs138410635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688776 | TTGCCTTCGTTCTAC[A/T]AATTCCCCCTTTCTG | 9870 |
rs138467492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74696959 | ACAAAGCAAGACTTC[A/G]TCTCAAAAAATAAAA | 9870 |
rs138712666 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AREL1 | GRCh38.p7 | 14:74674458 | TACAAAAAAATTAGC[C/T]GGGTGCGGTAGCTCA | 9870 |
rs138747098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671712 | TTTACATCATCACTT[C/T]GTTGGAAAGCTGAAG | 9870 |
rs138747563 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AREL1 | GRCh38.p7 | 14:74679554 | AAAATGGGCCGGGCA[C/T]GGTGGTTCATGCCTG | 9870 |
rs138770074 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | AREL1 | GRCh38.p7 | 14:74675643 | TTCTGCTACCAAATA[A/C]CAATTACACACAGGT | 9870 |
rs138782412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686068 | CCTTTTGGGAGTAAT[G/T]CAGCTAAGTAGAAAT | 9870 |
rs138924074 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74697892 | ATTCTATAACTCCCA[A/G]ATTTGGACACTGGGG | 9870 |
rs139120644 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74710750 | ATCAAAAATTCAGTG[A/C]CCACAGATATGTAAA | 9870 |
rs139207671 | snp | C/T | 5.01609e-05 | 0.00500779 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667547 | ATAGAAGATTTTATT[C/T]GCATTGGTGACTGGA | 9870 |
rs139238897 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74690750 | TTTAGTGTCCTTGAC[C/T]TTTATAAATATGGCA | 9870 |
rs139275819 | in-del | -/AAAG | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711761 | CTCCATTTTACAGAT[-/AAAG]AAACTGAGATGCAGA | 9870 |
rs139288796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74670912 | ATGACTCTGCCCTCC[C/T]TCCTCTTACCACTTT | 9870 |
rs139511611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686850 | GGGAACATTAGAATT[A/G]TCACGTGGATGAAGG | 9870 |
rs139619016 | snp | C/T | 0.00395161 | 0.044274 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676206 | TATGAAATGCAAGCA[C/T]GGAAGCAGCCTCGAG | 9870 |
rs139643401 | snp | C/T | 3.31851e-05 | 0.00407326 | intron-variant | AREL1 | GRCh38.p7 | 14:74672796 | TTCAATTGGAAAACT[C/T]TGGTATCTGCTGACA | 9870 |
rs139653930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74689934 | CGTTTTTTCATTTTA[A/G]AGTGGTAATGAGTAG | 9870 |
rs139669171 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676669 | CATCTCGGGGTACTA[C/T]TTGAAGGGTGTGCGG | 9870 |
rs139825023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74686391 | AAGACTTCAATCTTA[A/G]TTACTCATTTGATCA | 9870 |
rs139832284 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74683077 | AAAAGTGACTACTAA[C/T]ATGTATGGGGTTTCT | 9870 |
rs139896692 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AREL1 | GRCh38.p7 | 14:74672659 | GGAGGATCACAGCCC[A/G]GGAAGATCGAGGCTG | 9870 |
rs140074364 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668680 | GCTGGGAATCCCATA[A/C]TTTCCAGAAAGGATA | 9870 |
rs140075290 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713719 | TAGCTGCTGAGCGAT[A/C]ACACTGGGAAAGGCG | 9870 |
rs140095297 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | AREL1 | GRCh38.p7 | 14:74711007 | GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCG | 9870 |
rs140183986 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | AREL1 | GRCh38.p7 | 14:74681545 | TTTGGGAGGCTGAGG[C/T]GAGCGGATCATGAGG | 9870 |
rs140221276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687628 | CCCTGGACAAGTCAT[C/T]TAATCTTTGTAAAGG | 9870 |
rs140221756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74675064 | GAAAATTTCAAACAC[A/G]TACTAAAGAAGACAA | 9870 |
rs140225904 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | AREL1 | GRCh38.p7 | 14:74677015 | TGTGTTAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 9870 |
rs140239552 | snp | C/T | 0.00774305 | 0.0617379 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684549 | GGTAATTTCCCCGCA[C/T]GTAGTCATAAATAGT | 9870 |
rs140245216 | in-del | -/AAAT | 0.462582 | 0.131564 | intron-variant | AREL1 | GRCh38.p7 | 14:74694176 | CCAGACCCAGTCTCA[-/AAAT]AAATAAATAAATAAA | 9870 |
rs140256693 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667101 | CTTTCATTTATTTAT[C/G]CCTTAAGCTAATATC | 9870 |
rs140514959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700988 | GGGGCTACTGGTCCA[A/G]TGGAGTAGCTATACA | 9870 |
rs140608744 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662951 | CCAGCCATATGCCTA[A/G]GCATGCCCCACTCTG | 9870 |
rs140710636 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74665325 | GCTCACTGCAACCTC[C/T]ACCTCTCCACCTTGC | 9870 |
rs140759201 | in-del | -/C | 0.0755793 | 0.179102 | intron-variant | AREL1 | GRCh38.p7 | 14:74670581 | TTTTTGCTTATTTTA[-/C]AGATGAAATAATAAA | 9870 |
rs140877130 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74691021 | AGTTGAGATTCAAGC[C/T]GGGCTGGGAAAGCCT | 9870 |
rs141027612 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681806 | AGAAAGAAACAGGTT[-/G]GGGGGGGATAGGTGT | 9870 |
rs141113334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670671 | GGACACAGGTTGTCA[G/T]GTTCCCAGATCAGTT | 9870 |
rs141186944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706802 | GTGTAGTAAAATCTA[G/T]GAGGTGAGCATAGAG | 9870 |
rs141206776 | in-del | -/AATA | 0.410568 | 0.191619 | intron-variant | AREL1 | GRCh38.p7 | 14:74679845 | AAAAAAGAAAATAAT[-/AATA]AATAAATAAATAAAT | 9870 |
rs141224961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74701641 | CATATCATTCCACCC[C/T]GGCCCCTCCCAAATC | 9870 |
rs141228941 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74703877 | GATTGCTGGGTCATA[A/T]GGTAAGTATCTACTT | 9870 |
rs141303903 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | AREL1 | GRCh38.p7 | 14:74691355 | AAAAAAAAAGCCTAC[A/G]TCTAACTCCGAAGCT | 9870 |
rs141315233 | snp | A/T | 0.000150164 | 0.00866368 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664015 | TGTTGTGAACTGAAG[A/T]AGCCGAGCCAACTCC | 9870 |
rs141340264 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AREL1 | GRCh38.p7 | 14:74688300 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 9870 |
rs141384418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710539 | GAATAACTGACCATG[C/T]TATTTTAGCTTTTAG | 9870 |
rs141405253 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | AREL1 | GRCh38.p7 | 14:74680949 | GCACCTTGGGAGGCC[A/G]AGGCAGGAGGATTGC | 9870 |
rs141416427 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74692409 | AAAAATCAAAGAGAA[C/G]GTAGAACAGGCAGTG | 9870 |
rs141452535 | in-del | -/AT | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74698022 | TGTTAAATCAAACTC[-/AT]AGATAATAAAACAGA | 9870 |
rs141521914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698342 | TTGCTGCAGGAACAC[A/G]TGTCATTTATCTTCT | 9870 |
rs141598829 | snp | C/T | 1.67108e-05 | 0.00289052 | upstream-variant-2KB, utr-variant-5-prime, missense | AREL1, FCF1 | GRCh38.p7 | 14:74713513 | AAACAAGGAAGTATG[C/T]GACCATGAAGCGAAT | 9870 |
rs141718687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74685749 | AGTGTATGGCGTGAG[C/T]CAAACAACTCTCTCT | 9870 |
rs141724241 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74674226 | TAACCTTTCCTCTCC[A/G]TGGACAAAAGTAATA | 9870 |
rs141764128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671597 | ACTACGACTGCCTGA[A/G]GGAGATATGTTACTC | 9870 |
rs141811112 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74672254 | GCCAGTAAGTAAACT[G/T]CTCTTCCCTCGATAA | 9870 |
rs141912310 | in-del | -/GA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699377 | TGTGTGTGTGTGTGT[-/GA]GAGAGAGAGAGAGAG | 9870 |
rs142080322 | snp | A/G | 0.0329836 | 0.124112 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714268 | AAACCAGCCTGGCCA[A/G]CACGGTGAAACCCTG | 9870 |
rs142116724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712296 | GTTTACAGACACCCA[A/G]AGGGTCCACGGATGG | 9870 |
rs142395224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686787 | AGTTTCATACAAATC[C/T]TACTTAGAGTGATTA | 9870 |
rs142437297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673891 | TTAGTGAGGAGATAA[C/T]GATGCTTTATTTGGC | 9870 |
rs142462448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74691674 | TTGCTTAATACTACA[A/G]CATTTTGGCTCACAT | 9870 |
rs142504541 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711850 | CCCATCAGTCAGACT[C/G]CAAAGTTCGTGTTAA | 9870 |
rs142541926 | snp | C/G/T | 0.00159649 | 0.0282165 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713352 | AAGCGGTGACTGTTA[C/G/T]GCTTTACAGAGTGGG | 9870 |
rs142627701 | snp | A/C/G | 0.000281503 | 0.0118607 | intron-variant | AREL1 | GRCh38.p7 | 14:74663842 | AAGGGCAAGGGAGAA[A/C/G]TGATTAACTCATACC | 9870 |
rs142677726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74671880 | ATGATCTATCCACTA[A/G]ACATATTTATCCACA | 9870 |
rs142700204 | snp | A/G | 0.000299053 | 0.0122244 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667328 | ACTTACCTCAAGCTC[A/G]TTCTCATCAAAAATA | 9870 |
rs142774254 | in-del | -/A | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711236 | AACTAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9870 |
rs142892455 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74676503 | GAAGGAAAGAGAGAT[A/C/T]GAAGTGAATTAGGTG | 9870 |
rs142943556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693258 | CAGTCTGCTCCCTTC[A/G]TGCCCACATATGCAT | 9870 |
rs143128954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74688180 | ACAGGTGCCTGCCAC[C/T]ATGCCCAGCTAATTT | 9870 |
rs143133360 | in-del | -/GAGA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700876 | AGATGTTTTTTAACC[-/GAGA]GAGAAAAAGGATCAC | 9870 |
rs143155880 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AREL1 | GRCh38.p7 | 14:74686223 | TTTATGCTGTTACCA[A/G]TCAGACAAACTAATG | 9870 |
rs143227780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686868 | ACGTGGATGAAGGTG[C/T]TCCCAAAAGGGTCTA | 9870 |
rs143233375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692006 | CCATGTTGTACATCC[C/T]AATAACTAAAGCTTA | 9870 |
rs143377610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74672689 | GCAGTGAGCCATGAT[C/T]GCACCTCTGCACCCC | 9870 |
rs143396384 | in-del | -/AC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697156 | GATCCTGTCACACAT[-/AC]ACACACACACACACA | 9870 |
rs143404443 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74709573 | GAATGAATGACCAAG[C/T]GGCAGTAATCTATCT | 9870 |
rs143563102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711357 | CCAGCCTTGCCAACA[C/T]GGTGAAACCCATCTC | 9870 |
rs143578044 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | AREL1 | GRCh38.p7 | 14:74666683 | ATAGGATTTTATAGA[C/T]GGTACATGATATTAA | 9870 |
rs143587417 | snp | A/G | 0.000757563 | 0.0194476 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713135 | TGCCGGAAGCAGTAT[A/G]TGAATGACGTAGAAG | 9870 |
rs143604781 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74707089 | TATACACGATCTGGT[C/T]GGGCACAGTGACTCA | 9870 |
rs143676539 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74696847 | CACACACCTGTAATC[A/C]CAGCTACTCAGGAGA | 9870 |
rs143736847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74668693 | TAATTTCCAGAAAGG[A/G]TATCTGATTATCAGT | 9870 |
rs143783088 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74702539 | GCCTTCAAAACCATT[G/T]TTTCCTCCTAGGCCT | 9870 |
rs143798222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689065 | GTCAGCCAGGCTGCT[A/C]TTGAACTCCTGACCT | 9870 |
rs143836502 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686567 | AGGCTGTCAATGTTA[C/T]CTTGACCCAACACCT | 9870 |
rs143955856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74693764 | GCCTCTCCACTATGG[G/T]AAACCAAGGAAGAAA | 9870 |
rs143978572 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | AREL1 | GRCh38.p7 | 14:74690797 | GCTAGAAGAAAAATA[C/T]GACAGTAGTAAATTA | 9870 |
rs144108108 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74710925 | CAAGTTCCAGTGCAA[C/T]TATGTTAAAATAAAA | 9870 |
rs144247751 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74706577 | CTCAACACTTACCTA[C/T]TCAAAACAAAATTTC | 9870 |
rs144272891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680838 | CCTAGGGTGCTGAAG[C/T]GGTAAGTAAGTATAT | 9870 |
rs144375329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686595 | CCTTTTATCAGCACT[A/G]GAATATTACGTAGAG | 9870 |
rs144426845 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AREL1 | GRCh38.p7 | 14:74690111 | AACAAATTAGCTGGG[C/T]GTGCTGGCACACACC | 9870 |
rs144560323 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663088 | ATTTCCAGAAATGCC[C/T]GAAGGGAAAGTGCTT | 9870 |
rs144574176 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706363 | GAATGGTCACACGTA[C/T]ACTTAAAAGCTAACT | 9870 |
rs144603744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683835 | AACCACCAATGCTGC[C/T]TCCTTGGTCTTACCA | 9870 |
rs144844777 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | AREL1 | GRCh38.p7 | 14:74689892 | TGAGCCACCATGCCC[A/G]GCCTAGCACTTTTAT | 9870 |
rs144965485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74664181 | TGTGCCCCAGTTACC[A/G]TTCTATGAGGACACA | 9870 |
rs145017232 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74668043 | ACATTCTTTTATCTC[A/T]AATGTGAGTCAACAG | 9870 |
rs145077704 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | AREL1 | GRCh38.p7 | 14:74688094 | GCAGTGGTGTGATCT[C/T]GGCTCACTGAAAGCT | 9870 |
rs145102880 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74697855 | CAGAAATCTACTGTG[C/T]TGCCGTATTAGACTG | 9870 |
rs145219935 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AREL1 | GRCh38.p7 | 14:74673706 | TGGTGCTTCTAAAAG[A/G]AGTTAGCTTCAGCAC | 9870 |
rs145275793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699587 | TATACATACTGCTCT[A/C]ATTTATTTTAATATG | 9870 |
rs145513228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684888 | GTCCTCAGGCCAAAG[C/T]CCACCCACTGCCTAT | 9870 |
rs145528466 | snp | A/C/G | 0.0221141 | 0.102801 | intron-variant | AREL1 | GRCh38.p7 | 14:74677079 | GCTGGGATTACAGGC[A/C/G]TGAGCCACCACGCCC | 9870 |
rs145636056 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663229 | CTCCTATCTGTCCCC[C/G]TCTCTCCTGGCTCCT | 9870 |
rs145637746 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74701513 | ACCACAAGAACAGTA[C/T]GTGGGAAACTGCCTC | 9870 |
rs145702059 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | AREL1 | GRCh38.p7 | 14:74681739 | GGCACCACTACACTC[C/T]AGCCTGGCGACAGGG | 9870 |
rs145715354 | in-del | -/ATAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694202 | TAAATAAATAAATAA[-/ATAA]TGCCAACAGACTTGC | 9870 |
rs145773146 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74695715 | TGTTTATATAGCAGT[A/C]TCTCCTAATAGATTG | 9870 |
rs145824577 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74671627 | CATAAACAAGCTTTA[A/G]TGATACCACCTGACA | 9870 |
rs145855072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74665628 | ATTGAACTTTTACTA[C/T]CTTCCCTTCAGCTTC | 9870 |
rs146007853 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713698 | AGCCAGTGTTTAACA[G/T]TAATTTAGCTGCTGA | 9870 |
rs146016002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74675511 | AAATTGTTTTGACAC[A/G]GCACAAGAAGCCAAC | 9870 |
rs146080487 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74710974 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 9870 |
rs146203316 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74690428 | GATAGAGTTTGAAAG[A/G]ATTTCTCTAACAGTA | 9870 |
rs146251659 | snp | C/T | 0.000119308 | 0.00772269 | intron-variant | AREL1 | GRCh38.p7 | 14:74676101 | CAGGCAAAGAAACGG[C/T]TGAAGAACAGCACTA | 9870 |
rs146314656 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667631 | GACAAGGGAGAGGCT[-/G]GTGGATGGAAATTTA | 9870 |
rs146323884 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74672714 | CACCCCAGCCTGGGC[A/G]ATAGAGTGAGACCCT | 9870 |
rs146559865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74701627 | GGACACAGCCAAACC[A/G]TATCATTCCACCCCG | 9870 |
rs146577625 | snp | A/G/T | 0.00597534 | 0.0543715 | intron-variant | AREL1 | GRCh38.p7 | 14:74706773 | CAAATAAATAATTAC[A/G/T]TAGTTATACTTCCGT | 9870 |
rs146677684 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74683868 | CCTTTATATTATCAA[C/T]GCTAACCCAAATTTA | 9870 |
rs146800657 | snp | A/G | 0.00126105 | 0.0250786 | intron-variant | AREL1 | GRCh38.p7 | 14:74664931 | ACATCAGCAGCTGGA[A/G]AAAGATGGTAAGGTG | 9870 |
rs146818855 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669363 | TCGGTGGGATAGATG[C/G]AGATATGTGTCTTTT | 9870 |
rs146950260 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74708903 | ACAGTCTTCAAAAGA[C/G]CCACCAGGAAAACAT | 9870 |
rs146987698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74691629 | CTCTAGTGCAGAAAT[A/G]TCACTTGCTTACGAA | 9870 |
rs147050051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688685 | TGTCCCACTGCTCTA[C/T]AACAGCTCTCAAACC | 9870 |
rs147067928 | snp | A/G | 0.00233556 | 0.0340929 | upstream-variant-2KB, missense, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714924 | AAGAAGGATCCCAGC[A/G]CATTAAAGGAAAGAG | 9870 |
rs147091821 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74674239 | CCATGGACAAAAGTA[A/G]TAATTTAGTGAGTAC | 9870 |
rs147137836 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74666760 | AGTCTTACTCTGTTG[C/T]CCAGGCTGGAATGCA | 9870 |
rs147148245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709692 | GTTAATTGAAAAATA[A/C]TTAACAGCGACTAAT | 9870 |
rs147148297 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662455 | GATTTTGAATCTTGA[A/C]ATTATTTTCAATCAA | 9870 |
rs147210043 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | AREL1 | GRCh38.p7 | 14:74705186 | CTGGGATTATAGGCA[C/T]GCGTCACCACGCCCA | 9870 |
rs147381282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703887 | TCATATGGTAAGTAT[C/T]TACTTAACTTACAAG | 9870 |
rs147454210 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74686280 | AAAGACCAAGGAGAG[A/G]AACAAAAGGAGACTG | 9870 |
rs147464033 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | AREL1 | GRCh38.p7 | 14:74681047 | AAAAATTAACCGAGC[A/G]TGGTGGTGCACACTT | 9870 |
rs147626024 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | AREL1 | GRCh38.p7 | 14:74695238 | GTGCGTACTACTATG[C/T]CCAGCTAGTTTTTGT | 9870 |
rs147642533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74699947 | GCCTTGGGGGACAAG[A/G]CTGTATGCACAGACC | 9870 |
rs147747724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74682597 | ATCTGGTTTAGATAT[C/T]TGTACCCTCCAAATC | 9870 |
rs147958378 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74673910 | GCTTTATTTGGCAAC[A/G]AATCCTGTGTACACT | 9870 |
rs148002517 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74666340 | TGTGAGCAACAGGCC[A/C]CAACAAATTGATGTT | 9870 |
rs148064092 | snp | C/T | 0.00143216 | 0.0267213 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713171 | CGCCGTTGGTGATTA[C/T]GGAAGAACCAGGAGT | 9870 |
rs148150414 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660884 | ATTACCTCTGGATAG[C/T]AACTTACCTATTTCC | 9870 |
rs148214108 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | AREL1 | GRCh38.p7 | 14:74703477 | GACACAGCCAAACCA[C/T]ATCAAAAGATAATGA | 9870 |
rs148272946 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710187 | CCACTTTCATTTCAC[A/G/T]CTATAAGAACCTCAG | 9870 |
rs148288777 | snp | C/T | 0.00445618 | 0.0469918 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692287 | TCCTGGACTTCTCTC[C/T]AGTGCAGGGTGCAAT | 9870 |
rs148328252 | in-del | -/AA | 0.00755907 | 0.0610114 | intron-variant | AREL1 | GRCh38.p7 | 14:74697532 | CCAAAATCCCACCAT[-/AA]AAGATTGCCCTCCTC | 9870 |
rs148443518 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663301 | GTACCAGTCTGGTCA[A/C]GTAGTGAGGGCCAAA | 9870 |
rs148532274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706569 | AGGAGAAACTCAACA[C/T]TTACCTATTCAAAAC | 9870 |
rs148657091 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74700501 | TTTGAAATTTTAGCC[A/G]GGCGCAGTGGCTCAC | 9870 |
rs148801184 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AREL1 | GRCh38.p7 | 14:74686779 | CCGTCAAAAGTTTCA[C/T]ACAAATCCTACTTAG | 9870 |
rs148847269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677223 | AGAGAGGCCAGGTGC[A/G]GTGGCTCACACGTGT | 9870 |
rs148915647 | in-del | -/TAAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679851 | GAAAATAATAATAAA[-/TAAA]TAAATAAATAATAAT | 9870 |
rs148920767 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74695947 | CACAGGTAATGCTGA[C/T]GCTGCTGGTCTCCTA | 9870 |
rs149067099 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74683728 | TCTAAAGAAAACCAT[C/G/T]AAGTCATGAGCAAAT | 9870 |
rs149118782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688119 | AAAGCTCTGCCTCCC[A/G]GGTTCGCGCCATTCT | 9870 |
rs149192723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74708716 | TGAAATAAATGCCTT[C/T]GCTCTGAAAAACATG | 9870 |
rs149215911 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74673851 | GGCATGCGTCCTTCC[A/C]GAATTTATATATTCT | 9870 |
rs149240919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | AREL1 | GRCh38.p7 | 14:74698809 | TGGGAGGATGGCTTG[C/T]GCCCAGGAGTTCAAG | 9870 |
rs149245207 | snp | A/C/G | 3.64378e-05 | 0.00426821 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713077 | GGAACCGGCTCGGGG[A/C/G]ATTGCCCTTTCCCCA | 9870 |
rs149405811 | in-del | -/GTG | 0.0344721 | 0.12668 | intron-variant | AREL1 | GRCh38.p7 | 14:74698885 | AAAAAAAAGCTGGGT[-/GTG]GTGGTATGCACCTAT | 9870 |
rs149459971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74675439 | CTTTACTCCAATCCT[A/G]TAGCCTAATAGTGAC | 9870 |
rs149494130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74693710 | GTCAAACTCAGACAA[C/T]CTGGACCCAGAATCC | 9870 |
rs149511723 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74680779 | TACCTACATGATACT[C/T]AAAGGAAATGCTCAC | 9870 |
rs149606203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74666092 | TTTGTTTGGATTTCA[C/T]ATCTGAAGATATAAA | 9870 |
rs149714260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706100 | CTTGATGTGTTTTCT[A/G]TATACAAAACTGACT | 9870 |
rs149830672 | snp | C/G | 0.00238189 | 0.0344278 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683422 | TGGAATTGGGCTCCT[C/G]AAGGACTTCCTGGGT | 9870 |
rs149926757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667785 | CAGGGTTCCTACCAC[C/T]ATTGCTGTATACTAG | 9870 |
rs149977977 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673300 | CTATCCTGTGTACCA[A/G]CCAACAACAATAAGT | 9870 |
rs150086102 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712388 | AGAATTGTTCCTGGC[C/T]TTCCACAAACTTTCA | 9870 |
rs150093719 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | AREL1 | GRCh38.p7 | 14:74672311 | TTTAGTAGAATCAAA[-/T]AGAAGAACAGACATA | 9870 |
rs150207026 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | AREL1 | GRCh38.p7 | 14:74695610 | AGGACTCTTCCCACA[C/G]CAGATAGAATCAGCC | 9870 |
rs150244457 | snp | C/T | 5.31769e-05 | 0.00515612 | intron-variant | AREL1 | GRCh38.p7 | 14:74670712 | GAATCCTTGTTAGTC[C/T]ACCCATGATAACATA | 9870 |
rs150295596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74675215 | TTTTTAAATGAAGAA[C/T]GGTACACAGCAAAGT | 9870 |
rs150527989 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74698597 | TCAATGAACTTGGTC[C/T]GCCATGGGAGAAGGA | 9870 |
rs150559854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672406 | TTTATAAGTATATCT[A/G]TATCTTTACTTAAAC | 9870 |
rs150623747 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74689493 | TAGGAAAAATCCTAT[C/T]CACTCTCTCCAAAAT | 9870 |
rs150644312 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74676504 | AAGGAAAGAGAGATC[A/G]AAGTGAATTAGGTGT | 9870 |
rs150738091 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661504 | AAAGAACTGGCCAAA[A/C/G]TAAGAAACACTAATA | 9870 |
rs150790238 | snp | A/G | 1.66092e-05 | 0.00288172 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667334 | CTCAAGCTCATTCTC[A/G]TCAAAAATAGCCAAA | 9870 |
rs150801167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710665 | TGCTCCAGAAAGATT[A/T]GGAACTTCTAGTGAC | 9870 |
rs150844876 | in-del | -/AAG | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74710519 | ATGAGTCAAATGTTT[-/AAG]AAGAATAACTGACCA | 9870 |
rs150853572 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74715100 | ATCAATTCTAGTGGT[C/T]TGAAGGTTTTGGGAT | 9870 |
rs150890898 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74686842 | TCCACACTGGGAACA[A/T]TAGAATTGTCACGTG | 9870 |
rs150897334 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74692711 | GTTTTTTTGTTTTTG[C/T]TTTTGTTTTTGAGAC | 9870 |
rs150943077 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74690846 | ATTGAGTCACTTATC[A/G]CAGGCCAAACACTGC | 9870 |
rs150960765 | in-del | -/C | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74666201 | CTAAAATTACTTTTT[-/C]CCCCCATTTTAAAAG | 9870 |
rs151053775 | snp | A/G/T | 3.31188e-05 | 0.00406921 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663955 | AATAATCTGAAATGA[A/G/T]GGACAGAGGGCGGCA | 9870 |
rs151112577 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74670459 | AAGATCTAGTACAGG[A/G]ATCATTTGCTTCAGG | 9870 |
rs151122439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711785 | GAGATGCAGATAGAT[C/T]AACTCACCCAATGTC | 9870 |
rs151203845 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664818 | CAAATCCAACTGAAA[A/G]AAGTTTGGTCCATTT | 9870 |
rs151270899 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | AREL1 | GRCh38.p7 | 14:74700655 | CATGGTGGCACACGC[C/T]TGTATTCCCAGCTAC | 9870 |
rs151321943 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74707126 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGCGGG | 9870 |
rs180758095 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74675596 | AACTAGTTAACAATC[A/T]TGCCCTGATTCTCAG | 9870 |
rs180762080 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74696809 | ATCACTACTAAAATA[C/T]GAAAATTAGCCACGC | 9870 |
rs180788880 | snp | C/G/T | 0.00239401 | 0.0345304 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714361 | TTATTATTCTCAGCC[C/G/T]TTAGTGTGGATGTAT | 9870 |
rs180828610 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705196 | AGGCATGCGTCACCA[A/C/T]GCCCAGCTAATTTTG | 9870 |
rs181124001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696207 | TTAAAGCTACACAAC[C/T]ACCTTATATAAACAA | 9870 |
rs181129391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704952 | CTCCTGCATTCCATT[G/T]ATCTCATAGTCATTA | 9870 |
rs181130814 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74674930 | GTATAGGGGAAGGTC[C/G]TCACACAAAAAAGTT | 9870 |
rs181151268 | snp | G/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713843 | GTCCGTATAGTTCTC[G/T]TTATGTTTTTACCAT | 9870 |
rs181152619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686749 | CCCACAGAGAGTAGG[A/T]AATTTGAGGAATGAC | 9870 |
rs181156639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74665742 | TGTCCTAATTTGGTT[C/G]AGGATCCAGCATGTT | 9870 |
rs181289245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708691 | GCATCTCAACAGTAA[C/T]AAGCTGCACTGAAAT | 9870 |
rs181521751 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660761 | CTTCTTAGGAGCAGT[A/C]TTTTTGTTTGCCACT | 9870 |
rs181528132 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AREL1 | GRCh38.p7 | 14:74707863 | TTGGGAGGCTGAGGC[A/G]GGAGAATGGCGTGAA | 9870 |
rs181537175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689974 | TCCTCCAGGCTGGGC[A/T]TGGTGGCTCATGTCT | 9870 |
rs181547606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74681941 | GGAAAATGTTACCAT[C/T]GCAGGAAACTGGGAA | 9870 |
rs181588494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74690595 | CAGCATGCTCTACTT[C/T]TTGCTATTCATAATT | 9870 |
rs181738705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668745 | ATTTTTCAATCATTC[C/T]TATTCTGCTTTTAAC | 9870 |
rs181766238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671180 | TCTCCAAGTCCCTGT[A/G]TGTCTGTGTACCACA | 9870 |
rs181768164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74691746 | AGGGACTGTTAGAAA[A/G]TTGATTAACATACAT | 9870 |
rs181782371 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74701529 | GTGGGAAACTGCCTC[C/T]GTGATTCAATTATCT | 9870 |
rs181796612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74709814 | TATAACTTTCTAACA[C/T]TGAAATACAAGATGT | 9870 |
rs181973466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700766 | GTCTGGGCGACAGAG[C/T]GAGAGTCCCTCTCAA | 9870 |
rs182052265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664304 | CTCCAATTTACTACT[C/T]CTGTGGCAGTCAGCA | 9870 |
rs182063758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704691 | CATTTTGCAAATATT[A/T]TCTGTGGCTTGCCTC | 9870 |
rs182085092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74686301 | AAGGAGACTGTACTT[C/T]TCATCCTCAGTCATG | 9870 |
rs182226375 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | AREL1 | GRCh38.p7 | 14:74680488 | CAGCCACTCTGGAAA[A/C]GAATTTGGCAATTTA | 9870 |
rs182252510 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698179 | CCTTTACCACTAGAG[A/G]TACTTGAGCCAAAAC | 9870 |
rs182265124 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74678015 | ATAGTACAGATGTCA[A/C]TTTTCCCCAAATTGA | 9870 |
rs182324664 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AREL1 | GRCh38.p7 | 14:74677001 | AGACGGGGTTTCACT[A/G]TGTTAGCCAGGATAG | 9870 |
rs182413174 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697361 | CCAGCCATGAGTCCA[A/G]GGACATGAACTTAAA | 9870 |
rs182498431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686840 | AATCCACACTGGGAA[C/T]ATTAGAATTGTCACG | 9870 |
rs182575970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677087 | TACAGGCGTGAGCCA[C/T]CACGCCCGGCTGGAA | 9870 |
rs182682564 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74702218 | AGCTTCAACCCCACA[C/T]TTCCCCCCAACATTG | 9870 |
rs182696443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682499 | TGATGAAAGGATAAA[A/T]AAAATACGGCATGTA | 9870 |
rs182772416 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666200 | ACCTAAAATTACTTT[C/T]TCCCCCATTTTAAAA | 9870 |
rs182847429 | snp | C/T | 0.00201866 | 0.0317058 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683483 | AGAGATGTGAACTCT[C/T]AGTCCCACAGGCCGA | 9870 |
rs182847903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74668177 | AATTATTTGGCCTGA[A/G]CTTTCCTCTCTGCAA | 9870 |
rs182865178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710124 | CTACCTCCCAGCTTC[A/G]CATCCCCCACTTTCC | 9870 |
rs182865908 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662344 | CTGGTTTTGGCAATA[A/C]AGATGGCTTGTAATA | 9870 |
rs182866762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697669 | CTCCAGTCTCTTAAT[C/T]ATTCCTGTGGGTCTT | 9870 |
rs182877030 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74702820 | CCACAGATTTCTAGG[C/G]CAGGAGCAAAATGAT | 9870 |
rs182990187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706987 | AGGGTCAATGACTCT[C/G]TTCAACACTCGTCAG | 9870 |
rs183007297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672746 | TCTCCCAAACAAAAA[C/T]AAAAACAAAAACAGT | 9870 |
rs183034015 | snp | A/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711318 | GCCGAGGTGGGCAGA[A/T]CACCTGAGGTCAGGA | 9870 |
rs183158279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687984 | GGTTAAAAACTCATC[C/T]TAAAATAATTCGTCC | 9870 |
rs183242690 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687671 | CTTATATGTACCTCA[C/T]GGGGTGCTGTGAGGA | 9870 |
rs183262583 | snp | C/T | 1.66004e-05 | 0.00288096 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667346 | CTCATCAAAAATAGC[C/T]AAAAGGTTCTCAGGG | 9870 |
rs183277317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705887 | TCATTCTCAGCACAG[C/T]TTAGAGAAAGCAGGA | 9870 |
rs183399575 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692133 | CACCTTGTCTTCCAA[C/T]TTCCACATGAAAGAA | 9870 |
rs183467001 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74700014 | GCCAGGCCACAATAG[C/G]CCAACCCACAGCAAG | 9870 |
rs183590496 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74672113 | AAAGTGACAACAAAA[A/G]TCATTTCCTTTTAAT | 9870 |
rs183609996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680278 | TCACCAAAGGATACA[C/T]AGATGACAGACAGGC | 9870 |
rs183733248 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74702734 | GGCTGCAAATTTTCC[A/C]AACTTTTATGCTCTG | 9870 |
rs183738445 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662153 | TGAGTGAGGTCAGCA[C/G]CCATGTGCCAAGAAA | 9870 |
rs183890311 | snp | A/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712246 | TATGAATAAAGTGAC[A/T]AGTACAGTATACAGG | 9870 |
rs183901695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693645 | GAAACTGGGACACAG[A/G]AAGGTTAAAGTACTT | 9870 |
rs183928194 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | AREL1 | GRCh38.p7 | 14:74678493 | CAGAGTGAGACCCTG[A/C]CTCAAAAAAAAAAAA | 9870 |
rs183949162 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74682780 | AAAGCCCAGCACCTC[C/T]TCCCTCTCTCTCTCT | 9870 |
rs184018467 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74685063 | AAAAGTTTGCAAACT[C/G]TTGCTCTATATGAGC | 9870 |
rs184053982 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74703298 | CAATGAGAGCCAAGC[A/G]AAAGGGGAAATCCCT | 9870 |
rs184057030 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74674947 | CACACAAAAAAGTTC[A/T]TACAAAAGAGGAAAA | 9870 |
rs184077830 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699350 | AGTGACAGTGAGGGG[G/T]GTGTGTGTGTGTGTG | 9870 |
rs184342653 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688729 | ATAGTATTTACTGAC[C/T]TCCCAGTTTCACCCA | 9870 |
rs184422612 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679252 | ACATGGCAAAGCCCC[A/T]TCTCTACAAAAAATA | 9870 |
rs184431815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668491 | TTTAATGTAAGCATT[A/T]CTATCTAGGAGACTG | 9870 |
rs184434096 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AREL1 | GRCh38.p7 | 14:74699842 | ACTGAGAAAAGAAAC[A/G]AATCCGCTGCTCTTG | 9870 |
rs184449455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74707241 | GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 9870 |
rs184450822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74663885 | GGGCATGCATCAGGC[A/G]GGCAGATACCTACCA | 9870 |
rs184499514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74703658 | ATACATGTTGTTACA[C/T]ATTTCGGTAGTTCAC | 9870 |
rs184618339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685890 | TGACCACTCTAGGAA[C/T]ACCACAAACAGCCAC | 9870 |
rs184868056 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713888 | CCCCTGGGGTGGGGC[C/G]AGGGGAGTGTTTCTT | 9870 |
rs184914086 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662797 | ACTGTTCTAATCTTT[C/T]GCTACAAAATTTTCT | 9870 |
rs184941159 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74696466 | TAAAACTAGTATCTC[A/G]GGGACCAAATACTGT | 9870 |
rs184967530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74707668 | GTGTGGTGGTGGGCG[C/T]CTGTAGTCCCAGCTA | 9870 |
rs184976761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74668638 | CTCAGGAAGTTGGGT[C/T]TAATCCCATGTGTAC | 9870 |
rs184980494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689450 | CCTTTTATTCTCTAT[A/G]CATGGAAAATCTCCT | 9870 |
rs185144315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74702304 | ATTCAGGAGTTTCCA[C/T]ACATCCTCTGAAATC | 9870 |
rs185149186 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74695455 | TGATTATTAAATCAA[A/G]TAACTCCTAGTTGTA | 9870 |
rs185195487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676868 | GTGGCGCAATCTCGG[C/T]TCACTGCAAGCTCTG | 9870 |
rs185233962 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74697081 | GCCCAGAAGTTTGAG[A/G]CTACAGTGAGCTGTG | 9870 |
rs185242089 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714724 | TTATTTGCTCAGAAA[C/G]AGTATGCTGATATTA | 9870 |
rs185271026 | snp | A/G | 0.000131783 | 0.00811628 | upstream-variant-2KB, utr-variant-5-prime, missense | AREL1, FCF1 | GRCh38.p7 | 14:74713198 | GAGTTTGGCGTGACC[A/G]TGGTGAGAGAAGACG | 9870 |
rs185283912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74674292 | CTCTCTATTTAAAAA[G/T]GCAAATTAAAAATAT | 9870 |
rs185303547 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707935 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACCT | 9870 |
rs185307617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669540 | TTGGGTGTTTAATAG[A/T]CAACACAAATATGGA | 9870 |
rs185412594 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74690478 | TTGTAAGTTCCTCAA[C/T]CTAAAAGTTGCCAAT | 9870 |
rs185630105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697687 | TCCTGTGGGTCTTCT[A/G]TGAACTCTCTCCAGC | 9870 |
rs185757925 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690799 | TAGAAGAAAAATATG[A/G]CAGTAGTAAATTAAC | 9870 |
rs185779862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74704978 | CATTAAGTTTTATTC[C/T]CCTTGTTTCTTTCAA | 9870 |
rs185795264 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661858 | CAACTCAATCTCCAG[A/G]ATCAGTCTCTGGAAG | 9870 |
rs185898529 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74704806 | GTTTGTGGTTTTTGT[G/T]TTCTATTTTTTAAAA | 9870 |
rs185917693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686340 | GGTAGGAGTCTGAGG[A/G]AAGACTTTCACTGTT | 9870 |
rs185926284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708908 | CTTCAAAAGAGCCAC[A/C]AGGAAAACATCACTA | 9870 |
rs185929840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682654 | TGGAGGTGGGGCCTG[C/G]TGGGAGGTGATGGGG | 9870 |
rs186076243 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664396 | ATCATTTTTTTTTCC[C/G]AGAAAACATATCAAC | 9870 |
rs186114939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705591 | TGGCTTTAACGAGAG[A/T]CTTTTATAAGATCAT | 9870 |
rs186125230 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74667015 | GTGAGCCACCATGCC[C/T]GGCCTCAGTGATACT | 9870 |
rs186178232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709918 | ACCAATTAGTGAATG[A/G]AATGAAGTCCAAGCC | 9870 |
rs186225412 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661006 | TCCTTCTTCAGAAAC[C/T]GAGCATAAACACTTG | 9870 |
rs186240272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74687293 | GAAAAATTCCCACCT[A/G]CTATCTCTGACAACT | 9870 |
rs186241814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702095 | CCTGAGGCTTTTCCA[C/G]GCACATGGTACAAAC | 9870 |
rs186257680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681960 | GGAAACTGGGAAAAG[C/G]GTACACCAGATCTCT | 9870 |
rs186347749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671738 | TGAAGTTGTTTTTTT[A/C]TTTTCCTTTTGTTTT | 9870 |
rs186355613 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AREL1 | GRCh38.p7 | 14:74691784 | AATCCTCTGCTTTTT[C/T]GGAGTATAAAGATTT | 9870 |
rs186468147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686766 | ATTTGAGGAATGACC[A/G]TCAAAAGTTTCATAC | 9870 |
rs186582336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697426 | GTTAGGGTGGTCTAA[C/T]TAAGGAGGTTCCAAG | 9870 |
rs186631279 | snp | A/C/T | 6.63884e-05 | 0.00576113 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673097 | TTCTTATGCAGGGAG[A/C/T]GGATAAAAGTGGCTG | 9870 |
rs186655772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74665770 | GTTACTTAGCAGACT[G/T]CAAGTACTCATCCAA | 9870 |
rs186664449 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74693408 | TCAGTTTATAACTCT[C/T]GAAGATATTCATGAA | 9870 |
rs186778475 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74677005 | GGGGTTTCACTGTGT[C/T]AGCCAGGATAGTCTC | 9870 |
rs186807416 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | AREL1 | GRCh38.p7 | 14:74689034 | TTTTTTTTTAGTAGA[A/G]ACAGGGTTTCACCAT | 9870 |
rs186959889 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74698286 | TGCTATGTTTCCCCA[C/T]CCTAGATATCTATAT | 9870 |
rs186971772 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74668514 | GGAGACTGAGAAATA[A/T]ATTATTAAGATTTAG | 9870 |
rs186979954 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678018 | GTACAGATGTCAATT[C/T]TCCCCAAATTGATAT | 9870 |
rs187087908 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677234 | GTGCGGTGGCTCACA[C/T]GTGTAATCCCAGCAC | 9870 |
rs187228949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74687892 | AAAGGCATGGCTTCT[A/G]TTACTGTCCCTGAAC | 9870 |
rs187243367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667956 | TCTAAGCAACTAAGA[A/G]TAAAATCAGATAAGC | 9870 |
rs187251646 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74681213 | ACATTCCTATACCAC[A/G/T]TTTGGAGAGAAAAAA | 9870 |
rs187260197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706039 | CTGTCCCATTCTTAA[C/T]CCTAAATCTAGAAAA | 9870 |
rs187392909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703001 | TTCAAACTTTCCCAC[A/T]TTTTCCTGTCTTCCT | 9870 |
rs187522875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683656 | AATCCCAGTACCTAC[C/T]CTGTTCCTCACAGTC | 9870 |
rs187535242 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662749 | AGAACACCAAGCAGA[A/G]AGAGAATCAGGGATT | 9870 |
rs187569668 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AREL1 | GRCh38.p7 | 14:74700853 | TTTAAGCAACAACAA[C/T]AACAAAAAGATGTTT | 9870 |
rs187596086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707261 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCCGG | 9870 |
rs187732892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711780 | AAACTGAGATGCAGA[C/T]AGATTAACTCACCCA | 9870 |
rs187823576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693744 | CTTTTAATGACTACT[C/T]TACTGCCTCTCCACT | 9870 |
rs187829817 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712816 | GAGAATGTGTTCCCC[C/T]AAACTACTGGGCAAA | 9870 |
rs187834007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673670 | AACAACAAACAAACA[A/G]TGTATTTTAATATAT | 9870 |
rs187921820 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74688269 | TGACCTCGTGATCCA[C/T]CCGCCTCAGCCTCCC | 9870 |
rs188033138 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74675547 | TTTTTATGCTAGCAA[G/T]AAATTTTTAACAGTT | 9870 |
rs188211493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706988 | GGGTCAATGACTCTC[C/T]TCAACACTCGTCAGA | 9870 |
rs188235475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699407 | AGAGCAAGAGCAAGA[C/G]AGAGAGAGAGAGACA | 9870 |
rs188477779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679931 | CCTGTAATCCCAGCA[A/C]TTTTTGGGGCCAAGG | 9870 |
rs188482172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699900 | AGGAGAATTGCTTGA[A/G]ACTGAAACTTTACAC | 9870 |
rs188532810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679064 | GCCACCACACCCAGC[A/T]AATTTATAAATTTTT | 9870 |
rs188534339 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74672458 | AAAAGATAACCAGAT[C/G]AGGCATGGTAGCTCA | 9870 |
rs188577024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710591 | AATCACCAAGAGATA[C/T]ATCAAAAAACTGGTT | 9870 |
rs188661007 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713976 | TCAAATATTTTTGTC[A/G]GAGAAAATGGGAAAA | 9870 |
rs188677282 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74683027 | TCCACAGAGGCAGCA[A/G]ATGAGTGGCTGCCTA | 9870 |
rs188849890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692897 | TGTTTTTTGTAGAGA[C/T]GGGGTTTTGCCATGT | 9870 |
rs188956520 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707743 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 9870 |
rs188965821 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74702764 | GCTTCCCTTTTAAAT[C/G]TAAGTTCCAATTTCA | 9870 |
rs188966721 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74668666 | TACAAAGGCAGACAG[C/T]TGGGAATCCCATAAT | 9870 |
rs188969970 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662156 | GTGAGGTCAGCACCC[A/G]TGTGCCAAGAAAGGA | 9870 |
rs188971710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689834 | CTCCCAACCTGAGGT[G/T]ATCCGCCTGCCTCAG | 9870 |
rs189030078 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662943 | TCTCCAAGCCAGCCA[C/T]ATGCCTAGGCATGCC | 9870 |
rs189067051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74703367 | ATGAGAACAGTATGA[A/G]GGAAACCACCCCATG | 9870 |
rs189079961 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665412 | TATTTCTGATGAACA[C/T]CCTAAGAACTGCTAC | 9870 |
rs189101685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704871 | TGGTTTTTTTCTAGA[A/G]GGTTATCTAAACGTT | 9870 |
rs189116817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686564 | CTAAGGCTGTCAATG[C/T]TATCTTGACCCAACA | 9870 |
rs189180152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74680314 | AAAAGATGTTCAATA[A/G]CATTAACTATTTAAG | 9870 |
rs189318106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685468 | CAATGCCAACTCTGT[C/G]AAGGTACATTCTGGC | 9870 |
rs189323401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714820 | ATTTTTGAGATTTTA[A/G]TTGCTGTGGTTTTTC | 9870 |
rs189402492 | snp | C/T | 1.67357e-05 | 0.00289268 | missense | AREL1 | GRCh38.p7 | 14:74664019 | GTGAACTGAAGTAGC[C/T]GAGCCAACTCCTCCT | 9870 |
rs189497274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700303 | AACAGAAGCACAGAA[A/G]GCTAAAATGACTTGC | 9870 |
rs189522646 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74690587 | AGTTTCTACAGCATG[A/C]TCTACTTTTTGCTAT | 9870 |
rs189758500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670993 | CTCTGGTGTTTCTCC[A/G]TTGCGACTCATCTAA | 9870 |
rs189778139 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709535 | TTGCCCAGGACAGAA[G/T]GGGCCCTCAATAAAT | 9870 |
rs189808145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708046 | GAAAAAGGAAATTAG[C/T]GGAGAAACTTGTGAA | 9870 |
rs189817804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669544 | GTGTTTAATAGACAA[A/C]ACAAATATGGAACAT | 9870 |
rs190011424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74674330 | ATGGCCAAGTGTGGA[C/T]GGCTCACATCTATAA | 9870 |
rs190025683 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713610 | GTCTAGAGAGGATAA[A/G]TAGTAAAAATGTTTG | 9870 |
rs190203219 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661479 | TACCTGGGTCACAAG[A/G]ACATAAATAAAAGAA | 9870 |
rs190223531 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74702149 | GGTCTGGAGGACGGT[A/G]GCCCTCTTCTCACAG | 9870 |
rs190237062 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682092 | CACTGGTGGCAAAGA[C/G]GTGGGTGATGATAAT | 9870 |
rs190242950 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74695761 | ACACTGACCAGGTCA[C/T]AACATTGCCTCCCCA | 9870 |
rs190353475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74685960 | TCATCTTCTTAGATC[C/T]ATAGTTCCCAAGACA | 9870 |
rs190381352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677729 | GCTGGTCTCAAACTC[C/T]CCACCTTGTAATTTG | 9870 |
rs190392028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74697982 | TCACTAGAGGATGAG[C/T]GACTGGGGAGAAAAA | 9870 |
rs190508785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701387 | AGGCCTCACAAATCA[C/T]GGTGGAAGGTGAAAG | 9870 |
rs190561529 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74687980 | AAAGGGTTAAAAACT[A/C]ATCCTAAAATAATTC | 9870 |
rs190593019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706953 | ACAAAACACTACCTA[C/T]GAAGTATTACTTATT | 9870 |
rs190612165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703843 | ATTTCATTTCTCTTG[A/G]GTAAATATCTAAGAA | 9870 |
rs190751123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74681643 | CTGGGCGTGGTGGCA[C/T]GTGCCTGTAATCCCA | 9870 |
rs190852739 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74682779 | AAAAGCCCAGCACCT[A/C]CTCCCTCTCTCTCTC | 9870 |
rs190871855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687482 | TATGATATGACTTCA[A/G]TGCAACTCCCCATGG | 9870 |
rs190879481 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697214 | AGTCCATTTCAAAAT[G/T]TTGGTGCATACAGAG | 9870 |
rs190890840 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667242 | CTGCATCTCATAAGA[A/G]AAGGTACACCAAGCT | 9870 |
rs190997219 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74693098 | CAGCACAGGGTCTGG[A/T]GCAACCACAAAGACA | 9870 |
rs190997529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692025 | AACTAAAGCTTAACT[C/G]AGTCTGTTACCTTAC | 9870 |
rs191032233 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74709971 | GTCCAATGCCTTGGG[C/T]GATTTTTTCTCTTCA | 9870 |
rs191097372 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662137 | TCCCGGACCCCAAGG[A/T]TGAGTGAGGTCAGCA | 9870 |
rs191228269 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74711105 | GCGTGTTGGCGCACG[C/G]CTGTAATCCCAGCTA | 9870 |
rs191293330 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74705156 | GCGATTCTCCTGCCT[C/T]GGCCTCCCAAGTAGC | 9870 |
rs191297073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666075 | AGCTGTGGAGAGTTC[A/T]TTTTGTTTGGATTTC | 9870 |
rs191408837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672545 | AGTTCGAGACCAGCC[A/G]GAGCAATATGGCAAA | 9870 |
rs191486683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684960 | ATTTATAAATTGTCT[A/G]TGGCTACTTTTGCAC | 9870 |
rs191500853 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662773 | AGGGATTGCTGGCAT[A/C]CTATTCTTACTGTTC | 9870 |
rs191507417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711905 | GGGTTATACAATGGT[C/T]ACCTTCTTTTTTAAA | 9870 |
rs191517797 | snp | A/G | 0.000165992 | 0.00910869 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673108 | GGAGCGGATAAAAGT[A/G]GCTGCTAGAATGTTC | 9870 |
rs191519521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703089 | ATATTTTCAGGTATC[C/T]TTACAGCACCGCCTC | 9870 |
rs191524221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693477 | ACACAAACAGCCACC[A/C]TAAGACAAATGAGAA | 9870 |
rs191613524 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | AREL1 | GRCh38.p7 | 14:74677006 | GGGTTTCACTGTGTT[A/G]GCCAGGATAGTCTCG | 9870 |
rs191841452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680234 | AAAAGAAAAGAAAAG[A/G]AAATGGACAAAAGAC | 9870 |
rs191871368 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699948 | CCTTGGGGGACAAGG[A/C]TGTATGCACAGACCA | 9870 |
rs191950557 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74697536 | AATCCCACCATAAAA[G/T]ATTGCCCTCCTCCAT | 9870 |
rs192044215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74671920 | TCAGACAGCGAGCCA[C/T]GCCACACGGAGAATA | 9870 |
rs192099572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74705802 | AGAGTTCTTCAGACC[C/T]GTATTTCTTTTTGTA | 9870 |
rs192149459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74667987 | AGTAAGGAAGTCTTT[C/T]TATGTCTCAGAAATT | 9870 |
rs192354062 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74668622 | TGCCTTACCATGCCA[G/T]CTCAGGAAGTTGGGT | 9870 |
rs192374527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707484 | TGGCTAAAATGGTGA[A/C]ATCCCATCTCTACTA | 9870 |
rs192391291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689092 | ACCTCAAGTGAACCA[C/G]CTGCCTTGGCTTCCC | 9870 |
rs192402867 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74685709 | CAACTCTGCCTCATA[A/G]CTATCTCAGAGTAAG | 9870 |
rs192631249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683071 | TGGGGGAAAAGTGAC[C/T]ACTAACATGTATGGG | 9870 |
rs192650656 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662232 | GCTCAGGAGGGCTTG[C/T]TCCTCATGATCCCTG | 9870 |
rs192651479 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74703469 | TGGGTGGGGACACAG[A/C]CAAACCATATCAAAA | 9870 |
rs192654896 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712849 | AGGAGTCTGAACCCC[C/T]CTACCCTTTTCCTCC | 9870 |
rs192753900 | snp | A/G | 0.0103295 | 0.0711199 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663089 | TTTCCAGAAATGCCC[A/G]AAGGGAAAGTGCTTT | 9870 |
rs192768069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74668461 | CTGTTGGTATGCACA[A/G]TCCTGGATTTTTTTT | 9870 |
rs192791439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706998 | CTCTCTTCAACACTC[A/G]TCAGAGGGGATTCTT | 9870 |
rs192942073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679162 | ACCTCAGAAAGTGGA[C/T]TTCATCAAAATTGAA | 9870 |
rs192992935 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688584 | AATTACTACTTTTTC[C/T]CCAAACAACTGTCTT | 9870 |
rs193005238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74698529 | CTATATACTGGGCTA[C/T]GTGATAAAAGCTAAA | 9870 |
rs193134957 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74702776 | AATGTAAGTTCCAAT[A/T]TCAGATCATCTCTCT | 9870 |
rs193141954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673842 | GTTTCTGTAGGCATG[C/T]GTCCTTCCAGAATTT | 9870 |
rs193175157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699811 | TTCAGTTGCCTCATA[A/T]GTAAAATGGAGATGC | 9870 |
rs193209998 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74678465 | ATCGCACCACTGCAC[A/T]CAGCCTGGGTGACAG | 9870 |
rs193290682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694945 | CGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 9870 |
rs199570201 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712056 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAAAAGAAA | 9870 |
rs199603594 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705057 | TGTTTTTTTTTTTTT[G/T]AGACGGAGTTTCGCT | 9870 |
rs199642728 | snp | C/G | 6.63504e-05 | 0.00575941 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676598 | CTCATGAATGGACAA[C/G]GTGTAATTGTGCTCA | 9870 |
rs199748740 | snp | C/T | 1.65927e-05 | 0.00288029 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670786 | GTTGTTGTCACTGAA[C/T]CGGGTGAAGAGCTGA | 9870 |
rs199819118 | snp | C/T | 0.000132518 | 0.0081389 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675846 | GGGTGGCAGGTGCCA[C/T]GGAGTGCTGCTACAG | 9870 |
rs199831228 | snp | C/T | 0.000232918 | 0.0107891 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670065 | CACTTGCCCACGAGC[C/T]GTCCCGCAAACTCAT | 9870 |
rs199854300 | snp | C/T | 0.000168751 | 0.00918406 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675902 | CAAAGTAAATGCTCA[C/T]GCCTGAAGTGGACAC | 9870 |
rs199862616 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668469 | ATGCACAATCCTGGA[-/T]TTTTTTTTTAATGTA | 9870 |
rs199970347 | snp | C/G | 0.00678911 | 0.0578659 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713040 | CACCAACAGACCCCA[C/G]AGTTGGTCTCCACCC | 9870 |
rs199980615 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74668784 | TACTGCAACTTTAGC[A/C/G]TCATCATTATCATTT | 9870 |
rs199980632 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714923 | AAAGAAGGATCCCAG[C/T]GCATTAAAGGAAAGA | 9870 |
rs200009478 | snp | A/G | 0.00216118 | 0.0328012 | intron-variant | AREL1 | GRCh38.p7 | 14:74671367 | AAGGTGCGAGTGGGG[A/G]GGAGAGTTCAAAAAG | 9870 |
rs200026472 | snp | C/T | 0.00299544 | 0.0385843 | intron-variant | AREL1 | GRCh38.p7 | 14:74673025 | GCCTCTCCACCCTCA[C/T]GGATGTGGCTGGGCT | 9870 |
rs200030575 | snp | A/T | 0.000100185 | 0.00707691 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714853 | CTCCCTTGGATTTAA[A/T]TTACCTTTTTCTTCC | 9870 |
rs200106908 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692265 | ATACAGCCCAAGAAT[A/G]TATCATTCCTGGACT | 9870 |
rs200179317 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712068 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAGAAAGA | 9870 |
rs200202003 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676700 | CTGCCCACAGGTCAA[C/T]ACAAGAGTAGAAAAG | 9870 |
rs200250433 | snp | A/G | 0.000819062 | 0.0202203 | intron-variant | AREL1 | GRCh38.p7 | 14:74676324 | CTTGAGGGCCGAGCT[A/G]TAGGAAGGCAACAGA | 9870 |
rs200368606 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678696 | AAGACATGTATAAGC[-/AA]AAAAAAAAAAAAAAA | 9870 |
rs200442820 | in-del | -/ATAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694205 | TAAATAAATAAATAA[-/ATAA]TGCCAACAGACTTGC | 9870 |
rs200571905 | snp | A/G | 4.97632e-05 | 0.0049879 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676597 | CCTCATGAATGGACA[A/G]GGTGTAATTGTGCTC | 9870 |
rs200612760 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712085 | AAAAAAAAGAAAGAA[-/AG]AAAGAAAGAAAAAGA | 9870 |
rs200776635 | snp | C/G/T | 3.95963e-05 | 0.00444937 | missense | AREL1 | GRCh38.p7 | 14:74664071 | TCCAAAACCACCTCA[C/G/T]GACCTGGCAGGGAGA | 9870 |
rs200778168 | snp | C/T | 0.000347754 | 0.0131817 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675768 | GTGGCACTCAGAGGG[C/T]GAGTCTTCATCTTCC | 9870 |
rs200783128 | snp | A/G | 9.94398e-05 | 0.00705053 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684517 | ATCCCAGGAGACTTT[A/G]CAAGACCGGGGATCC | 9870 |
rs200841641 | snp | A/G | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675769 | TGGCACTCAGAGGGC[A/G]AGTCTTCATCTTCCT | 9870 |
rs200860271 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74695029 | GAAAGAAAATGGTAT[A/G]AAGAAATTAAGATAA | 9870 |
rs200875941 | snp | A/G | 0.000729178 | 0.0190803 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713599 | TTCTAATAAGAGTCT[A/G]GAGAGGATAAGTAGT | 9870 |
rs201017145 | snp | C/T | 0.000217023 | 0.0104146 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676318 | CTTCTTCTTGAGGGC[C/T]GAGCTATAGGAAGGC | 9870 |
rs201169650 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | AREL1 | GRCh38.p7 | 14:74671268 | CCCTTTTCCTTGGGG[-/A]AAAAAAAAACCTAGG | 9870 |
rs201302274 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712078 | AAAAAGAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 9870 |
rs201313458 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682663 | GGCCTGGTGGGAGGT[A/G]ATGGGGTCATAGGGG | 9870 |
rs201366093 | snp | C/T | 6.6313e-05 | 0.00575779 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684488 | CTGTGGCCCACCTCA[C/T]AGGGGTCCTTCCAAT | 9870 |
rs201431051 | snp | A/G | 1.67318e-05 | 0.00289234 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713095 | TGCCCTTTCCCCAAG[A/G]AGTTTCCGCTTCCGG | 9870 |
rs201433610 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | AREL1 | GRCh38.p7 | 14:74667150 | ATTTTCACATTCTAA[-/T]TTTTTTAAAGGCTGA | 9870 |
rs201493223 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674601 | AGTGAGACCCTGTCT[C/T]AAAAAATAAAATAAA | 9870 |
rs201493689 | snp | A/G | 0.000132527 | 0.00813916 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676190 | GATTGGCTGATTTTG[A/G]TATGAAATGCAAGCA | 9870 |
rs201520700 | snp | A/C | 0.000473838 | 0.0153849 | intron-variant | AREL1 | GRCh38.p7 | 14:74676777 | AGACAATGGAATCTA[A/C]CATTTATTTATTTTA | 9870 |
rs201597260 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678057 | AACACAATTCTTATC[A/G]AAGTTCCAGCAAGAT | 9870 |
rs201603970 | snp | A/C | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714777 | GATTTCTTCAGTAGA[A/C]CAAAAAAAAAAAAAA | 9870 |
rs201605025 | snp | C/G | 5.01115e-05 | 0.00500532 | missense | AREL1 | GRCh38.p7 | 14:74664017 | TTGTGAACTGAAGTA[C/G]CCGAGCCAACTCCTC | 9870 |
rs201650386 | snp | A/G | 9.95421e-05 | 0.00705416 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670788 | TGTTGTCACTGAACC[A/G]GGTGAAGAGCTGATT | 9870 |
rs201728233 | snp | A/G | | | upstream-variant-2KB, splice-acceptor-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713483 | AAAATTTCTGTTTCA[A/G]GGGGAAGCAAAAGAA | 9870 |
rs201735885 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688020 | ATACTGAGTACTTAC[A/T]TTTTTTTTTTTTTTT | 9870 |
rs201739319 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698625 | GGACAATGCAATGTT[G/T]CAAGTGCCATAAAAG | 9870 |
rs201741583 | snp | C/G | 0.000629077 | 0.0177241 | missense | AREL1 | GRCh38.p7 | 14:74663740 | GCATGCCAAAGCCCT[C/G]GCAACCCTCGCTGAT | 9870 |
rs201806783 | in-del | -/AGAAAAGAAAAG | 0.0154538 | 0.0865337 | intron-variant | AREL1 | GRCh38.p7 | 14:74680205 | AAAGAAAGAAAGAAA[-/AGAAAAGAAAAG]AGAAAAGAAAAGAAA | 9870 |
rs201903994 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671284 | AAAAAAAAACCTAGG[-/T]TTTTTTTTTTAGGGA | 9870 |
rs201916897 | snp | A/G | 1.73051e-05 | 0.00294147 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670118 | GGGGCGATTAGGGTT[A/G]GGATGCACCTGTCCA | 9870 |
rs201922193 | in-del | -/GGA | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74694749 | AATCCCAGCACTTTG[-/GGA]GGCTGAAGCGGGCGG | 9870 |
rs201925398 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690265 | AAGACCCTGTCTCCA[-/C]AAAAAAAAAAAAAAA | 9870 |
rs201992401 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712082 | AGAAAAAAAAAGAAA[A/G]AAAGAAAGAAAGAAA | 9870 |
rs202043372 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667636 | AGGGAGAGGCTGTGG[C/T]TGGAAATTTATGAGA | 9870 |
rs202068887 | snp | C/T | 0.000984459 | 0.0221644 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692152 | CACATGAAAGAAAAA[C/T]GCCACAAGGTCAACA | 9870 |
rs202071581 | snp | A/G | 0.00301643 | 0.0387185 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673098 | TCTTATGCAGGGAGC[A/G]GATAAAAGTGGCTGC | 9870 |
rs202100309 | snp | A/C/T | 0.00152668 | 0.0275867 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673171 | AATGCCATCATCCAC[A/C/T]ACCAGTGTGAGCAGC | 9870 |
rs202106130 | snp | A/C/G | 0.000264959 | 0.0115073 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676683 | ATTTGAAGGGTGTGC[A/C/G]GCTGCCCACAGGTCA | 9870 |
rs202176590 | snp | A/C/T | 0.000381391 | 0.0138047 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684584 | TCCCCTCGGCGCTCG[A/C/T]GGTCCTCATTCTGGA | 9870 |
rs202185306 | in-del | -/ATAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679862 | TAAATAAATAAATAA[-/ATAA]TAATAATCCCATTAG | 9870 |
rs202185961 | snp | C/T | 3.31658e-05 | 0.00407208 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675862 | GGAGTGCTGCTACAG[C/T]TGGTAGCATTATAAA | 9870 |
rs367584983 | snp | C/T | 1.66109e-05 | 0.00288187 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670013 | GCGAGCTCGGACCAA[C/T]TGCTTGTAGGCTCCT | 9870 |
rs367606325 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674488 | ATGCCTGTAATCCCA[A/G]GTACTCGGGAGGCTG | 9870 |
rs367612242 | snp | G/T | 5.00113e-05 | 0.00500031 | intron-variant | AREL1 | GRCh38.p7 | 14:74685560 | GGACCCAAGCAACCT[G/T]TACAAAAATATAATA | 9870 |
rs367654486 | in-del | -/GAAAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680237 | GAAAAGAAAAGAAAA[-/GAAAA]TGGACAAAAGACACG | 9870 |
rs367694143 | snp | A/C | 1.67987e-05 | 0.00289811 | intron-variant | AREL1 | GRCh38.p7 | 14:74667270 | GCTGGTTCCTGTAAG[A/C]TACAAAAATGCCAAG | 9870 |
rs367709243 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691723 | AATACTTCAAAATAT[C/T]TGTCTCAAGGGACTG | 9870 |
rs367719185 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672863 | GTCTGCTGACCTTCA[A/G]GGTGACTTTGGAATG | 9870 |
rs367728211 | snp | A/C | 0.000375868 | 0.0137042 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714954 | GAAGTGTGAGTAATC[A/C]AACGTTTGAAGTTTT | 9870 |
rs367820129 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680472 | GGAATGTAAAATGCT[A/C]CAGCCACTCTGGAAA | 9870 |
rs367950623 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681760 | GGCGACAGGGCGAGA[C/T]GCCATCAAAAAAAAA | 9870 |
rs367955244 | snp | A/G | 1.73552e-05 | 0.00294573 | intron-variant | AREL1 | GRCh38.p7 | 14:74674115 | CACTGAGAATTGCTG[A/G]AGGACCAACAGACAG | 9870 |
rs367961105 | snp | C/T | 0.00177766 | 0.0297602 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685623 | TAAAACATCAGGTCC[C/T]GTCAATGCCAACAGA | 9870 |
rs367967810 | snp | G/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712379 | ATTTTTTAAAGAATT[G/T]TTCCTGGCTTTCCAC | 9870 |
rs367984367 | snp | A/G | 0.000545832 | 0.0165112 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713056 | AGTTGGTCTCCACCC[A/G]GCCTGGGAACCGGCT | 9870 |
rs368045409 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74702552 | TTTTTTCCTCCTAGG[A/C/T]CTCCAGGTCTGTGAT | 9870 |
rs368083512 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686992 | TAGCTGGGGACCCAA[A/C]AGCTATCATCTCAAA | 9870 |
rs368172762 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695282 | GCAGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 9870 |
rs368190321 | snp | A/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662544 | CATCATTCAACAGTG[A/T]ACCTAATAAGCTTCC | 9870 |
rs368224278 | snp | A/C | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714231 | GGCTGAGGCGGGTGG[A/C]TCACCTGAGGTGAGG | 9870 |
rs368285382 | snp | C/T | 4.97963e-05 | 0.00498955 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683526 | GGCTGCCCGTTCTTA[C/T]AGAATAACTGCCATG | 9870 |
rs368320038 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683078 | AAAGTGACTACTAAC[A/G]TGTATGGGGTTTCTT | 9870 |
rs368409592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74672667 | ACAGCCCGGGAAGAT[C/T]GAGGCTGCAGTGAGC | 9870 |
rs368573336 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668828 | ACCACAATGTAAATA[A/G]AAGCACATGCATCGG | 9870 |
rs368595105 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710213 | CTCAGATTGCAATAA[A/T]ATTACAATGCAACAA | 9870 |
rs368595833 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673771 | ATCTTCTCTATTAAC[A/T]TAGTCTTGAAGGCAA | 9870 |
rs368604464 | snp | C/T | 3.31538e-05 | 0.00407134 | missense | AREL1 | GRCh38.p7 | 14:74664917 | GTCTCCAGTCCCACA[C/T]ATCAGCAGCTGGAAA | 9870 |
rs368788722 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690395 | ATCAGGAATTTTCCA[G/T]ATGGGATCTTCCTTG | 9870 |
rs368788804 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670253 | ATCAGAGCCCATCCA[A/G]ATGTTAGTTTTTTGG | 9870 |
rs368818205 | snp | A/C | 1.65765e-05 | 0.00287888 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676742 | TTTGGTCTTAGAAGG[A/C]ACCACCATTCCTGGA | 9870 |
rs368858691 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74711099 | AGCCAGGCGTGTTGG[C/T]GCACGCCTGTAATCC | 9870 |
rs368920387 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664515 | CTGCAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 9870 |
rs368969437 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712078 | AAAAAGAAAAAAAAA[-/G]AAAGAAAGAAAGAAA | 9870 |
rs368988876 | snp | C/G | 0.000167986 | 0.00916322 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669635 | GGACCCAGAGGCTTT[C/G]TCCTCTTTCTCACCT | 9870 |
rs369011085 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683766 | TTGTTCAGAGGACAA[A/G]GGTAGAATTTACCAC | 9870 |
rs369094495 | snp | C/T | 0.000437904 | 0.0147905 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713270 | AGGAGGTAGTCAGAC[C/T]GTGGCCAAATTTCCT | 9870 |
rs369147178 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702047 | CAGGGTACAGCCTCC[A/T]CCCCAGCTGCTTTCG | 9870 |
rs369153110 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684628 | ACGTGCGGCAAGCTC[A/C]AAGAGGAACTTAATT | 9870 |
rs369161965 | snp | A/G | 6.62361e-05 | 0.00575445 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663741 | CATGCCAAAGCCCTC[A/G]CAACCCTCGCTGATG | 9870 |
rs369175156 | snp | C/T | 1.66087e-05 | 0.00288168 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673183 | CACCACCAGTGTGAG[C/T]AGCTTATGGACAGGG | 9870 |
rs369218469 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671346 | TTTTTTTTTTTTTTT[-/G]TGGAGAAGGTGCGAG | 9870 |
rs369285766 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703855 | TTGGGTAAATATCTA[A/G]GAATGGGATTGCTGG | 9870 |
rs369300359 | snp | A/G | 0.000163987 | 0.00905353 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683484 | GAGATGTGAACTCTT[A/G]GTCCCACAGGCCGAT | 9870 |
rs369305151 | snp | A/T | 0.000165986 | 0.00910854 | missense | AREL1 | GRCh38.p7 | 14:74667367 | GTTCTCAGGGACCAA[A/T]TCATTCAGGCCTGAA | 9870 |
rs369310377 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681488 | AAGAACAGGTTGGGG[A/G]TGGGGGGCAGGTACG | 9870 |
rs369397490 | snp | A/C/G | 0.000151417 | 0.00869975 | intron-variant | AREL1 | GRCh38.p7 | 14:74673248 | CAAAGAAATTAATCT[A/C/G]TAAAACCCTCAAGGC | 9870 |
rs369413261 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688139 | CGCGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 9870 |
rs369448420 | snp | A/C | 1.79274e-05 | 0.00299389 | intron-variant | AREL1 | GRCh38.p7 | 14:74675956 | CATCCTCTGAAGTAT[A/C]ATAAGGAATAAGGTT | 9870 |
rs369473016 | snp | A/G | 5.52003e-05 | 0.0052533 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713443 | ACTTTAAAAGATGCC[A/G]TGTGTTTCCAACTTT | 9870 |
rs369496666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74703297 | ACAATGAGAGCCAAG[C/T]GAAAGGGGAAATCCC | 9870 |
rs369603208 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | AREL1 | GRCh38.p7 | 14:74663884 | TGGGCATGCATCAGG[A/C]GGGCAGATACCTACC | 9870 |
rs369612371 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712094 | AAAGAAAGAAAGAAA[A/G]AAAAAGAAAAAAAGA | 9870 |
rs369623547 | snp | A/G | 3.33611e-05 | 0.00408405 | intron-variant | AREL1 | GRCh38.p7 | 14:74685663 | ATCACAGCTGCAGCT[A/G]TTAAAAGAAAACTTG | 9870 |
rs369632012 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664448 | TTCTTCTTTTCCTTT[-/C]TTTTTTTTTTTTTTT | 9870 |
rs369636473 | snp | A/C/T | 8.28238e-05 | 0.00643474 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676218 | GCATGGAAGCAGCCT[A/C/T]GAGAATGCAGGGTGA | 9870 |
rs369652037 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711953 | CTTCCAACTCTAGGA[C/T]AGCATCATGCAATAA | 9870 |
rs369659712 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669875 | CTTAAAAATTATTTA[C/T]AAGCCCAGGAGGAGA | 9870 |
rs369736973 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689114 | TGGCTTCCCAAAGTG[C/T]TGGGATTACAAGCGT | 9870 |
rs369787790 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705745 | GCATTTCTTAATTCA[A/G]TTTGGATTCTCTCTA | 9870 |
rs369794633 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697860 | ATCTACTGTGCTGCC[A/G]TATTAGACTGTACCT | 9870 |
rs369895804 | snp | A/T | 0.000149354 | 0.0086403 | intron-variant | AREL1 | GRCh38.p7 | 14:74667451 | TTCAAGGCCAAGAAC[A/T]GACAGGATCCCACCT | 9870 |
rs369928782 | snp | A/G | 0.000100978 | 0.00710484 | intron-variant | AREL1 | GRCh38.p7 | 14:74670749 | ATTTTCCACCCACCC[A/G]TCACCAACTCACTAA | 9870 |
rs369946804 | snp | A/G | 3.33684e-05 | 0.00408449 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713546 | TTAGTCTCAGAGATC[A/G]GAGGCTGTGAGTGTC | 9870 |
rs370042147 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692441 | AAACCCTGGGACACT[A/G]AAAATAACCAAAAAT | 9870 |
rs370044149 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74715095 | CATATATCAATTCTA[A/G]TGGTTTGAAGGTTTT | 9870 |
rs370153266 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690491 | AACCTAAAAGTTGCC[A/C]ATTTAATTCAGTTCA | 9870 |
rs370203528 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700890 | CGAGAGAGAAAAAGG[A/G]TCACACATTTTAAAT | 9870 |
rs370307461 | snp | C/T | 1.67228e-05 | 0.00289156 | intron-variant | AREL1 | GRCh38.p7 | 14:74676325 | TTGAGGGCCGAGCTA[C/T]AGGAAGGCAACAGAG | 9870 |
rs370313422 | snp | C/T | 0.000298058 | 0.0122041 | missense | AREL1 | GRCh38.p7 | 14:74663966 | ATGAGGGACAGAGGG[C/T]GGCAAAGCCTCCAGG | 9870 |
rs370317425 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666181 | ATAAGAATTGGGCAA[A/G]ACCACCTAAAATTAC | 9870 |
rs370424019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74674516 | CTGAGGCACAAGAAT[C/T]GCTTGAACCCGGGAG | 9870 |
rs370443453 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671303 | TTTTTTTAGGGAGTG[A/G]GTAGGAGGTAAGAGT | 9870 |
rs370460576 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670998 | GTGTTTCTCCGTTGC[A/G]ACTCATCTAAACTGT | 9870 |
rs370475152 | snp | A/G | 8.41404e-05 | 0.00648561 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674069 | GGAAGGTGTAAAGGC[A/G]CCAGGGGATGATCTT | 9870 |
rs370493289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702985 | CAAGTCTCCAGGAAG[C/T]TTCAAACTTTCCCAC | 9870 |
rs370542506 | snp | C/T | 3.31669e-05 | 0.00407215 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684575 | ATAGTCCGGTCCCCT[C/T]GGCGCTCGCGGTCCT | 9870 |
rs370553304 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698263 | CATTTTAAATGATAT[A/T]ATTTTTCTGCTATGT | 9870 |
rs370567839 | snp | C/G/T | 5.07467e-05 | 0.00503698 | intron-variant | AREL1 | GRCh38.p7 | 14:74675686 | ATTTTATGTCGAGAA[C/G/T]GGAAGGTCCAACCTT | 9870 |
rs370581767 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689799 | CGGGGTTTCTCCATG[A/T]TGGTCAGGCTGATCT | 9870 |
rs370604316 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706084 | TCCTCTTCCCTCCTA[C/T]CTTGATGTGTTTTCT | 9870 |
rs370810374 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694967 | GCACTCCAGCCTGGG[C/T]GATAGAGTGAGACTC | 9870 |
rs370811935 | snp | A/G | 1.6566e-05 | 0.00287797 | missense | AREL1 | GRCh38.p7 | 14:74664879 | ACAACTACTGCATGG[A/G]CTTTGAAGTCAGACA | 9870 |
rs370850441 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708043 | ATAGAAAAAGGAAAT[C/T]AGTGGAGAAACTTGT | 9870 |
rs370877926 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700899 | AAAAGGATCACACAT[G/T]TTAAATGAAGTAACT | 9870 |
rs370923446 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680764 | CCAAAACATTTTGGG[C/T]ACCTACATGATACTC | 9870 |
rs370930472 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699175 | TTCAACACTGTTTTC[C/G/T]TATGATTTTGAGGAG | 9870 |
rs370935586 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691144 | GCAACATGGCAAAAC[C/T]CTGTCTCTACAAAAA | 9870 |
rs370956665 | snp | C/T | 1.68088e-05 | 0.00289899 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669975 | CGCAGTCCTATGATT[C/T]GGGCCAGGAAAGAGC | 9870 |
rs371025102 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662248 | TCCTCATGATCCCTG[C/T]GAACAGGAGGGCTCA | 9870 |
rs371068311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74701561 | CCACTGGATCCCTCC[C/T]ATAACACATGAGAAT | 9870 |
rs371078319 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678558 | GTGGTACTGGAGGAG[A/G]GATAGGTACACAGAT | 9870 |
rs371104320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694808 | TCCTGGCTAACACGG[C/T]GAAATCCCGTCTCTA | 9870 |
rs371128985 | snp | C/T | 1.77669e-05 | 0.00298046 | intron-variant | AREL1 | GRCh38.p7 | 14:74674002 | AGAGATGAAGCATGC[C/T]TGATGTGAACCAGAT | 9870 |
rs371163318 | snp | C/T | 2.73101e-05 | 0.00369517 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714959 | GTGAGTAATCAAACG[C/T]TTGAAGTTTTCCTTT | 9870 |
rs371199914 | snp | C/T | 1.65943e-05 | 0.00288043 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676280 | GGATGTTACTGATTT[C/T]TCAAATGAGACACCA | 9870 |
rs371243401 | snp | A/C | 1.66513e-05 | 0.00288537 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671415 | AAACTGACCTTCTTC[A/C]TCCTGGAAAACAACC | 9870 |
rs371289378 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671131 | AATGGACATTTCTCT[C/T]AAGGTAACCACGGTT | 9870 |
rs371296659 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713682 | TTATATAGCATGAGA[C/T]AGCCAGTGTTTAACA | 9870 |
rs371297358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74690990 | GCTGAACATCTCACA[C/T]TGGGGTAAGTGACAG | 9870 |
rs371301448 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711714 | ACATAAGTCCTGATA[A/G]CATCCCAATAAAAGA | 9870 |
rs371303553 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666466 | GAATGAATTTACTAT[A/G]TAAATAAAAATATAT | 9870 |
rs371310034 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691937 | ATTCTCACTGCAACT[A/G]TATACTTTAACAGCT | 9870 |
rs371335066 | snp | A/G | 0.000529898 | 0.0162686 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663688 | CAGAAGCTCCAGAGA[A/G]CATGGGAGCCAACTG | 9870 |
rs371337532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74664130 | CAAGCTAGGATTAGA[C/T]CCCTGGGGAAGGAAC | 9870 |
rs371350129 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701642 | ATATCATTCCACCCC[A/G]GCCCCTCCCAAATCT | 9870 |
rs371380466 | in-del | -/AAC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705508 | GGTTCTTAAAACAAC[-/AAC]TAAATTCCACAACCC | 9870 |
rs371385716 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689935 | GTTTTTTCATTTTAG[A/T]GTGGTAATGAGTAGT | 9870 |
rs371393954 | snp | C/T | 5.07464e-05 | 0.00503693 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684672 | CAACCACAGACACTG[C/T]GATTCCACCTATGCA | 9870 |
rs371419779 | snp | C/T | 3.39253e-05 | 0.00411844 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674043 | GCTTACTTTTGTTCC[C/T]GGACACACTCGGAAG | 9870 |
rs371425828 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695942 | AGGTTCACAGGTAAT[A/G]CTGATGCTGCTGGTC | 9870 |
rs371479808 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687941 | TTATACTATTCTAAT[A/T]TTATGCCTAAAAAAT | 9870 |
rs371512437 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681489 | AGAACAGGTTGGGGA[G/T]GGGGGGCAGGTACGG | 9870 |
rs371561437 | snp | A/G | 1.6604e-05 | 0.00288127 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670035 | TAGGCTCCTCCTAGA[A/G]AGGACTCATAGAGAC | 9870 |
rs371592546 | in-del | -/CAAAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700803 | CAAAACAAAACAAAA[-/CAAAA]AGGAATGTTAAAGGA | 9870 |
rs371594982 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661478 | GTACCTGGGTCACAA[A/G]GACATAAATAAAAGA | 9870 |
rs371610162 | snp | A/G | 0.000155988 | 0.00883005 | missense | AREL1 | GRCh38.p7 | 14:74663932 | AGCGTGCTATGGGTC[A/G]GAGCGGCAATAATCT | 9870 |
rs371624600 | snp | A/C | 3.29473e-05 | 0.00405864 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713191 | GAACCAGGAGTTTGG[A/C]GTGACCATGGTGAGA | 9870 |
rs371659563 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679344 | GGAGATCACCTAAGC[C/T]GGGAGAGGTCAAGGC | 9870 |
rs371725347 | snp | A/G | 3.46374e-05 | 0.00416143 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675927 | GGACACATTGCGTTC[A/G]ACGATATTCTTCTCA | 9870 |
rs371747758 | in-del | -/TTTTA | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74672371 | TTTAGTATATCTGTC[-/TTTTA]TAAGTATATCTGTCT | 9870 |
rs371749669 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683693 | ACAAAAACACAGAGA[G/T]AAACAAATCCCCTCA | 9870 |
rs371839334 | snp | A/C | 1.66239e-05 | 0.00288299 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685633 | GGTCCCGTCAATGCC[A/C]ACAGACAGCCGAGGA | 9870 |
rs371878455 | snp | C/T | 6.66678e-05 | 0.00577317 | intron-variant | AREL1 | GRCh38.p7 | 14:74667305 | GAATGGGAGTCTGAA[C/T]TGCAATCACTTACCT | 9870 |
rs371889400 | in-del | -/GT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686677 | TTTTTTTCAGGGTGT[-/GT]TTTTACATCTGATTG | 9870 |
rs371956338 | snp | C/T | 0.000165986 | 0.00910854 | missense | AREL1 | GRCh38.p7 | 14:74667371 | TCAGGGACCAATTCA[C/T]TCAGGCCTGAAACAA | 9870 |
rs371970631 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708960 | ACAGCTCAGGCATGC[A/G]TGTGTGTACACACAC | 9870 |
rs372055280 | in-del | -/C/TC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689591 | TCTTATAGCACTTTT[-/C/TC]CTTTTTTTTTTTTTT | 9870 |
rs372098960 | snp | A/G | 1.65993e-05 | 0.00288086 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675867 | GCTGCTACAGTTGGT[A/G]GCATTATAAAGATAA | 9870 |
rs372127621 | snp | A/G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669188 | GCCATGAGCCACTGC[A/G/T]CCCAGCCAAAAAGTT | 9870 |
rs372132290 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687104 | TTTAACTGCCTTAGG[C/T]ACTTCCTCAGCGGGA | 9870 |
rs372136508 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707405 | CAGTGGATCACACCG[A/G]TAATCCCAGCACTTT | 9870 |
rs372158022 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682658 | GGTGGGGCCTGGTGG[A/G]AGGTGATGGGGTCAT | 9870 |
rs372169069 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671971 | CAGTCACACCTACCA[C/G]AGCCAAACATCACAA | 9870 |
rs372180737 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683168 | TTAAACTGTATACTT[G/T]AAAAGGATGAATTTT | 9870 |
rs372197341 | snp | C/T | 3.65457e-05 | 0.00427452 | intron-variant | AREL1 | GRCh38.p7 | 14:74670167 | CCTGGGCCATTTTTC[C/T]TCAAGCCCAGTTCTG | 9870 |
rs372197748 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712082 | AGAAAAAAAAAGAAA[-/G]AAAGAAAGAAAGAAA | 9870 |
rs372272809 | snp | A/G | 1.66305e-05 | 0.00288357 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670063 | GACACTTGCCCACGA[A/G]CCGTCCCGCAAACTC | 9870 |
rs372327067 | in-del | -/AAAGAAAGAAAG | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712075 | AAAAAAAAGAAAAAA[-/AAAGAAAGAAAG]AAAGAAAGAAAAAGA | 9870 |
rs372352217 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AREL1 | GRCh38.p7 | 14:74682913 | CTTTTTGTACAACTT[A/G]CAGAACCATGAGCCA | 9870 |
rs372363536 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677703 | AGACAGCGTTTCACC[A/G]TATTGGCCAGGCTGG | 9870 |
rs372395020 | snp | A/G | 0.000299461 | 0.0122328 | intron-variant | AREL1 | GRCh38.p7 | 14:74683550 | TGCCATGGGGAGAAG[A/G]AGGACACCTGTTAGC | 9870 |
rs372405367 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686925 | TTGGGATCACAACTA[C/T]TGAACCTCCTTCCCA | 9870 |
rs372477648 | snp | C/T | 9.97904e-05 | 0.00706295 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670767 | ACCAACTCACTAATG[C/T]TTGGTTGTTGTCACT | 9870 |
rs372478964 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702740 | AAATTTTCCAAACTT[C/T]TATGCTCTGCTTCCC | 9870 |
rs372550458 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689592 | TCTTATAGCACTTTT[-/C]TTTTTTTTTTTTTTT | 9870 |
rs372574151 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700687 | GGGGAAGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 9870 |
rs372593008 | snp | C/T | 4.96767e-05 | 0.00498356 | missense | AREL1 | GRCh38.p7 | 14:74663936 | TGCTATGGGTCGGAG[C/T]GGCAATAATCTGAAA | 9870 |
rs372713200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679113 | CTATGTTGCCCAGGC[C/T]GGTCTTGAACTCCTG | 9870 |
rs372732998 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | AREL1 | GRCh38.p7 | 14:74710479 | ATGATATGCAATTTT[-/C]CCTCTGAACCTATAT | 9870 |
rs372755646 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant | AREL1 | GRCh38.p7 | 14:74669799 | CAGAAAGACACAGAA[C/T]AGAACATGAATACTC | 9870 |
rs372763423 | snp | A/C | 1.66145e-05 | 0.00288218 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673195 | GAGCAGCTTATGGAC[A/C]GGGTCAGGACCAAGG | 9870 |
rs372836699 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691637 | CAGAAATATCACTTG[C/T]TTACGAAGGTTCCTG | 9870 |
rs372865893 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704320 | GCCTCATGAGGTCCT[C/G]ACGACATGTGCCCAA | 9870 |
rs372880152 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684318 | TTTGTGACTCTTCAG[A/C]TAGTAGCAATTCACT | 9870 |
rs372896480 | snp | A/G | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661143 | ACTCTACCCCGAGCC[A/G]ACCACTTCAGGAGGA | 9870 |
rs373071991 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683963 | GGGTTCAGACTCTCA[A/G]GCCAAGCTTAATGCT | 9870 |
rs373079504 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712100 | AGAAAGAAAGAAAAA[A/G]AAAAAAAGAAATACA | 9870 |
rs373092010 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665444 | ATGGATTATTTTTAA[A/T]TGAAACAAAGGACAA | 9870 |
rs373105626 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705294 | TTCGCCCACCTCAGC[C/T]TCCCTAAGTGCTGGG | 9870 |
rs373173647 | snp | A/G | 1.7864e-05 | 0.00298859 | intron-variant | AREL1 | GRCh38.p7 | 14:74673995 | ATAGTCCAGAGATGA[A/G]GCATGCTTGATGTGA | 9870 |
rs373195544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671040 | AATCCCACCCCTTTT[G/T]GTAGGATTAATGGTA | 9870 |
rs373204125 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74705485 | AAGACCTCTGCACCC[-/CT]GATACTGGTTCTTAA | 9870 |
rs373223701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74692590 | TGAGAAGTGCCAGAG[C/T]TTCCTTCAGTTCACT | 9870 |
rs373383568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74699938 | ATATGGAGTGCCTTG[A/G]GGGACAAGGCTGTAT | 9870 |
rs373397978 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675009 | TCCCTTTTATCTGAA[C/T]GTGCAGGTCAGTTGT | 9870 |
rs373426524 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707271 | TACTCGGGAGGCTGA[G/T]GCCGGAGAATAGTTT | 9870 |
rs373435283 | snp | C/T | 4.9807e-05 | 0.00499009 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684461 | TCCCTTACATGCACT[C/T]GGAAGGCCATGCTGT | 9870 |
rs373484218 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713549 | GTCTCAGAGATCAGA[A/G]GCTGTGAGTGTCTGG | 9870 |
rs373607019 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702473 | CTGGAGCAACTGGGG[C/T]ACAGGGCACCAAGTC | 9870 |
rs373653295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694946 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 9870 |
rs373731594 | snp | C/T | 0.000167986 | 0.00916323 | intron-variant | AREL1 | GRCh38.p7 | 14:74685588 | ATAGAGAGAGCTCTT[C/T]CCATAACGTACCAAT | 9870 |
rs373767882 | snp | A/G | 1.68323e-05 | 0.00290101 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674079 | AAGGCGCCAGGGGAT[A/G]ATCTTCAGGTAGAAC | 9870 |
rs373768648 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702390 | ATCACGTGTAAGCTG[C/G]CAAGGCTTGGGGCTT | 9870 |
rs373790817 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant | AREL1 | GRCh38.p7 | 14:74676098 | AAACAGGCAAAGAAA[C/T]GGCTGAAGAACAGCA | 9870 |
rs373837829 | snp | C/T | 1.65578e-05 | 0.00287726 | missense | AREL1 | GRCh38.p7 | 14:74663905 | GATACCTACCATGTG[C/T]GTGCAGTAGGCAGCG | 9870 |
rs373853577 | in-del | -/GAAA | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711764 | CATTTTACAGATAAA[-/GAAA]CTGAGATGCAGATAG | 9870 |
rs373868674 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74695204 | CTTGCCTCAGCCTCC[A/C]TAGTGGCTGGGACTA | 9870 |
rs373923208 | snp | A/G/T | 0.000200701 | 0.0100156 | missense | AREL1 | GRCh38.p7 | 14:74667548 | TAGAAGATTTTATTC[A/G/T]CATTGGTGACTGGAG | 9870 |