SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs373988836 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678340 | TATTCCTACAAAAAA[C/G]ATAAAAAATTAGCTA | 9870 |
rs374037786 | snp | A/G | 1.72439e-05 | 0.00293627 | intron-variant | AREL1 | GRCh38.p7 | 14:74676371 | AGTATTTTCCCATTT[A/G]CAAGCCACTTTACTC | 9870 |
rs374039077 | snp | A/G | 0.000157987 | 0.00888644 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663994 | AGGTGGTAGCTGAGA[A/G]GAGCCTGTTGTGAAC | 9870 |
rs374130101 | snp | C/T | 3.37655e-05 | 0.00410873 | intron-variant | AREL1 | GRCh38.p7 | 14:74673254 | AATTAATCTATAAAA[C/T]CCTCAAGGCCAGTAA | 9870 |
rs374133829 | snp | C/T | 6.62405e-05 | 0.00575464 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683404 | AGGCCACTTTTACTA[C/T]GTTGGAATTGGGCTC | 9870 |
rs374137720 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675429 | GCCAAAATTTCTTTA[C/T]TCCAATCCTGTAGCC | 9870 |
rs374234569 | snp | A/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713778 | ACTTTTTCTACCGTT[A/T]TATGCTTTGTCTGCC | 9870 |
rs374246822 | snp | C/G | 0.000431969 | 0.0146901 | intron-variant | AREL1 | GRCh38.p7 | 14:74669898 | GGAGGAGAGATTTCA[C/G]GGTTAATGGCCAGGG | 9870 |
rs374349845 | snp | C/T | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676719 | AGAGTAGAAAAGTGG[C/T]ACACAATTTTGGTCT | 9870 |
rs374367717 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681824 | GGGATAGGTGTGGCT[-/G]GTAAAAGGGCAACAT | 9870 |
rs374368566 | snp | A/T | 1.65715e-05 | 0.00287845 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676255 | AGAACACCTGGAAAG[A/T]CTGCCTGTTGGATGT | 9870 |
rs374396821 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693563 | TCAGTGCTTCATACA[C/T]ATAAACTCACAGATA | 9870 |
rs374509831 | snp | C/T | 1.70049e-05 | 0.00291585 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674039 | TTCAGCTTACTTTTG[C/T]TCCTGGACACACTCG | 9870 |
rs374511972 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693582 | AACTCACAGATACAA[G/T]TATCCCTATTTTAAC | 9870 |
rs374516304 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696810 | TCACTACTAAAATAC[A/G]AAAATTAGCCACGCA | 9870 |
rs374521541 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665985 | CTTCAAAATGTAACA[A/G]AATTTACCAGTAGTT | 9870 |
rs374539009 | snp | A/C/G | 0.000293748 | 0.0121162 | intron-variant | AREL1 | GRCh38.p7 | 14:74669912 | AGGGTTAATGGCCAG[A/C/G]GGCCTTAGTAGGAAA | 9870 |
rs374541572 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690017 | CTTTGGGAGGCTGAG[A/G]TGGGAAGATCACTTG | 9870 |
rs374822205 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704554 | GGGGATGACTCTGAA[C/T]AGAATGAGACACAGA | 9870 |
rs374828033 | snp | C/T | 0.000115922 | 0.00761233 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672877 | AGGGTGACTTTGGAA[C/T]GTGGTCTTTTCATAT | 9870 |
rs374836019 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712068 | AAAAAAAAAAAAAAA[-/G]AAAAAAAAAGAAAGA | 9870 |
rs374847908 | snp | A/C | 0.000165986 | 0.00910854 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672840 | ACCTACCGATTCCAA[A/C]AAGGCATGTCTGCTG | 9870 |
rs374862176 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711277 | TGGCACAGTGGCTCA[C/T]GTCTGTAATCCCAGA | 9870 |
rs374921018 | snp | A/C | 8.37907e-05 | 0.00647212 | intron-variant | AREL1 | GRCh38.p7 | 14:74664971 | CAGTCAGAGAGACAA[A/C]GACCCAATATAAGGT | 9870 |
rs374936613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74702380 | CAGGCTCAACATCAC[A/G]TGTAAGCTGCCAAGG | 9870 |
rs374938656 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687948 | ATTCTAATTTTATGC[C/G]TAAAAAATTTTACAA | 9870 |
rs374941116 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74665099 | ATCAATTACATACAA[C/T]AGGGCAATAGTTGCT | 9870 |
rs374979700 | snp | A/G | 4.99073e-05 | 0.00499511 | intron-variant | AREL1 | GRCh38.p7 | 14:74685596 | AGCTCTTTCCATAAC[A/G]TACCAATAACGTAAA | 9870 |
rs374986772 | snp | C/T | 1.66048e-05 | 0.00288134 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670044 | CCTAGAGAGGACTCA[C/T]AGAGACACTTGCCCA | 9870 |
rs374993164 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689410 | CTTTTGAAAACTCAT[C/T]TCCTCTGCCTAGAAT | 9870 |
rs375033104 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692168 | GCCACAAGGTCAACA[G/T]AAAGGGTCTATCCAT | 9870 |
rs375036335 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666197 | ACCACCTAAAATTAC[C/T]TTTTCCCCCATTTTA | 9870 |
rs375063375 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689827 | TCTCAAACTCCCAAC[C/T]TGAGGTGATCCGCCT | 9870 |
rs375083338 | snp | C/T | 3.50465e-05 | 0.00418593 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675939 | TTCGACGATATTCTT[C/T]TCATCCTCTGAAGTA | 9870 |
rs375206789 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712090 | AAAGAAAGAAAGAAA[A/G]AAAGAAAAAGAAAAA | 9870 |
rs375239164 | snp | A/C | 1.65693e-05 | 0.00287826 | intron-variant | AREL1 | GRCh38.p7 | 14:74672980 | AAGATCCATCATTAC[A/C]GCCTCATTACAAGCC | 9870 |
rs375279507 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714466 | TTTTACATTTTAGCC[C/T]TTTATAAGAAGCATA | 9870 |
rs375280557 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663181 | CATGGCCTATGCCTA[C/T]CATTGTGCAGCGGGA | 9870 |
rs375287680 | snp | A/G | 0.000161987 | 0.00899817 | missense | AREL1 | GRCh38.p7 | 14:74664894 | GCTTTGAAGTCAGAC[A/G]CACTGATGTCTCCAG | 9870 |
rs375288415 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690995 | ACATCTCACATTGGG[G/T]TAAGTGACAGAGTTG | 9870 |
rs375303024 | snp | C/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662508 | TCATCTTCCAAGATA[C/G]AGCAGCAGGTACTCT | 9870 |
rs375304451 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686808 | AGAGTGATTATCTAA[A/G]GTCCTACTAGAAAAG | 9870 |
rs375408533 | snp | A/G/T | 5.35895e-05 | 0.00517613 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713463 | TTTCCAACTTTTTTA[A/G/T]TTCTAAAATTTCTGT | 9870 |
rs375481183 | snp | C/T | 0.000437904 | 0.0147905 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713106 | CAAGGAGTTTCCGCT[C/T]CCGGGCTATCCTTTG | 9870 |
rs375490934 | snp | G/T | 5.30415e-05 | 0.00514956 | intron-variant | AREL1 | GRCh38.p7 | 14:74670718 | TTGTTAGTCTACCCA[G/T]GATAACATAATCCAC | 9870 |
rs375549358 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74706111 | TTCTATATACAAAAC[A/T]GACTCTGCTATGCCT | 9870 |
rs375551740 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682840 | CTGCTCCCGCTTCGC[C/T]TTCCACCATGAGTGG | 9870 |
rs375603700 | snp | A/G | 1.67981e-05 | 0.00289806 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669614 | TACAGGAAACTGGAG[A/G]ACATAGGACCCAGAG | 9870 |
rs375607001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669324 | TTCACCATCATTCAG[C/T]TATTTTTCAACTGGA | 9870 |
rs375670104 | snp | C/T | 8.32938e-05 | 0.0064529 | intron-variant | AREL1 | GRCh38.p7 | 14:74683557 | GGGAGAAGAAGGACA[C/T]CTGTTAGCAAGCAGA | 9870 |
rs375712747 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671283 | AAAAAAAAACCTAGG[-/T]TTTTTTTTTTTAGGG | 9870 |
rs375733144 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696920 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAT | 9870 |
rs375743559 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703716 | TTAAATGGACATACT[A/G]CAATCTGTTTATCCA | 9870 |
rs375792805 | snp | A/G | 4.97822e-05 | 0.00498885 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670783 | TTGGTTGTTGTCACT[A/G]AACCGGGTGAAGAGC | 9870 |
rs375828087 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688998 | CCCACCACCACGCCA[A/G]GCTAATTTTTTGTAT | 9870 |
rs375845594 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700767 | TCTGGGCGACAGAGC[A/G]AGAGTCCCTCTCAAA | 9870 |
rs375852771 | in-del | -/AAAACAAAAACA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672748 | TCCCAAACAAAAACA[-/AAAACAAAAACA]GTAACCTGCAGAATA | 9870 |
rs375900833 | snp | A/G | 0.00038129 | 0.0138022 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684567 | AGTCATAAATAGTCC[A/G]GTCCCCTCGGCGCTC | 9870 |
rs375903720 | snp | C/T | 0.000182893 | 0.00956101 | intron-variant | AREL1 | GRCh38.p7 | 14:74669806 | ACACAGAACAGAACA[C/T]GAATACTCTTGCCCT | 9870 |
rs375910311 | in-del | -/TC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664447 | TTTCTTCTTTTCCTT[-/TC]TTTTTTTTTTTTTTT | 9870 |
rs375938931 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671701 | TCTGATTTGCCTTTA[C/T]ATCATCACTTTGTTG | 9870 |
rs375993687 | snp | C/T | 4.9928e-05 | 0.00499615 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671467 | GAGATGGAGAAATTC[C/T]GAGTGGCTTTCAGAG | 9870 |
rs376015649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687432 | CTGTAAAAAGAGTTG[C/T]AATTTAATAATTTCT | 9870 |
rs376065898 | snp | C/G | 3.3657e-05 | 0.00410212 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674066 | CTCGGAAGGTGTAAA[C/G]GCGCCAGGGGATGAT | 9870 |
rs376128972 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702227 | CCCACATTTCCCCCC[A/C]ACATTGCCCTAGCAG | 9870 |
rs376144017 | snp | C/T | 1.66252e-05 | 0.00288311 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670005 | CGGGTGAAGCGAGCT[C/T]GGACCAACTGCTTGT | 9870 |
rs376167577 | in-del | -/AGG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694751 | TCCCAGCACTTTGGG[-/AGG]CTGAAGCGGGCGGAT | 9870 |
rs376182850 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | AREL1 | GRCh38.p7 | 14:74671195 | ATGTCTGTGTACCAC[-/A]AGCTCCTCAATGCCA | 9870 |
rs376234292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692705 | GACACAGTTTTTTTG[C/T]TTTTGTTTTTGTTTT | 9870 |
rs376250238 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684983 | TTTTGCACTACACTG[A/G]CAGAGTTGAGTCATT | 9870 |
rs376251237 | snp | A/G | 1.69355e-05 | 0.00290989 | intron-variant | AREL1 | GRCh38.p7 | 14:74676535 | GAGAATAACAGAGAA[A/G]GGAGCCAGCTCTCTC | 9870 |
rs376469893 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697500 | CTTAATTCCACTCTT[A/G]GTTTATACTCCCCAA | 9870 |
rs376490763 | snp | C/T | 0.00027386 | 0.0116985 | intron-variant | AREL1 | GRCh38.p7 | 14:74678309 | CGAGACCACCCTGGG[C/T]AACATAGTGAGACCC | 9870 |
rs376513930 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701315 | AGACGTATCAGAGAC[C/T]GGTTAATTTACAAAG | 9870 |
rs376594122 | snp | C/T | 1.65762e-05 | 0.00287886 | intron-variant | AREL1 | GRCh38.p7 | 14:74667415 | AAGTCATACCCACAC[C/T]ATGGATACAGGTATT | 9870 |
rs376637591 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683229 | ATTATTTTTAAAAAG[G/T]AAAGACAGGATGGAA | 9870 |
rs376649199 | snp | A/C/G | 5.33123e-05 | 0.00516273 | intron-variant | AREL1 | GRCh38.p7 | 14:74671359 | TTGTGGAGAAGGTGC[A/C/G]AGTGGGGAGGAGAGT | 9870 |
rs376715219 | snp | C/T | 8.28e-05 | 0.00643375 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683429 | GGGCTCCTGAAGGAC[C/T]TCCTGGGTCACTGGA | 9870 |
rs376804131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688320 | GTGAGCCACCACGCC[C/T]GGCCCTGAGTACTTA | 9870 |
rs376915333 | snp | C/T | 8.27917e-05 | 0.00643343 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663931 | CAGCGTGCTATGGGT[C/T]GGAGCGGCAATAATC | 9870 |
rs376922025 | in-del | -/TTTTAT | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74688824 | TCAAAAGCCCTTCTA[-/TTTTAT]TTTTATTTTTATTTT | 9870 |
rs376937368 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661430 | GTCTCCTTCAAAGAC[A/G]CTAAAAGGCCAGAAG | 9870 |
rs377041259 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689539 | ATTTAGAAATTCCTT[C/T]CCTCATGTGAATCTC | 9870 |
rs377111196 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703100 | TATCTTTACAGCACC[A/G]CCTCACTCCCAGTAC | 9870 |
rs377140484 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677753 | TAATTTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 9870 |
rs377159591 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679653 | CTAACAGGGCAAAAC[C/T]CCATCTCTACTAAAA | 9870 |
rs377222659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704774 | TGATGAAAGCCAACA[C/T]AAATTTTTTCTTCAT | 9870 |
rs377234330 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74671279 | TGGGGAAAAAAAAAC[C/G]TAGGTTTTTTTTTTT | 9870 |
rs377236156 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692399 | TTCCCCAGAAAAAAA[G/T]CAAAGAGAAGGTAGA | 9870 |
rs377260912 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692849 | GCTGGGACTACAGGC[A/G]TGCACTACCACACCT | 9870 |
rs377337106 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666140 | GATTTTGATTCTTGT[C/T]CTCAAATCTACTTCA | 9870 |
rs377368325 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676661 | ATCATACTCATCTCG[A/G]GGTACTATTTGAAGG | 9870 |
rs377369051 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705370 | TCTGAATTTGGAAAG[A/T]TTTTAATATTTTAAC | 9870 |
rs377418415 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702508 | CACTGCACACAGCAG[C/G/T]GGGGACCTGGGCCCT | 9870 |
rs377420528 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663095 | GAAATGCCCGAAGGG[A/G]AAGTGCTTTTTCCAG | 9870 |
rs377428727 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661682 | AGTTCAGACAGAGAA[C/T]AGAAAACCACAATAG | 9870 |
rs377463485 | snp | C/G/T | 0.000116006 | 0.0076151 | synonymous-codon, missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676259 | CACCTGGAAAGTCTG[C/G/T]CTGTTGGATGTTACT | 9870 |
rs377487208 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685148 | AGAAGCAGTCAAAAG[C/G]ATGTGCCTTTGGTTC | 9870 |
rs377527987 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689741 | AGCTGGGATTACAGG[A/C]ATGCACCACCACGCC | 9870 |
rs377550107 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662207 | CTGAGGTCAGGCAGG[A/C]ACTGTAGCAGCTCAG | 9870 |
rs377622795 | in-del | -/GAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710524 | TCAAATGTTTAAGAA[-/GAA]TAACTGACCATGTTA | 9870 |
rs377686006 | snp | A/G | 8.94606e-05 | 0.00668747 | intron-variant | AREL1 | GRCh38.p7 | 14:74673993 | AGATAGTCCAGAGAT[A/G]AAGCATGCTTGATGT | 9870 |
rs377691368 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693989 | CAAGACCAGCCTGGG[C/T]GACATAACAAAACCC | 9870 |
rs377707918 | in-del | -/AC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665461 | GAAACAAAGGACAAA[-/AC]ACACACACACAAACT | 9870 |
rs377716020 | snp | G/T | 3.61696e-05 | 0.00425247 | upstream-variant-2KB, missense, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714881 | TCCTAGTAAAGAAAA[G/T]GATAGATTAAAACCT | 9870 |
rs377717041 | snp | C/T | 1.7447e-05 | 0.0029535 | intron-variant | AREL1 | GRCh38.p7 | 14:74671524 | TTGTCAGAACACTGG[C/T]TGGTGTCCTCTGGAT | 9870 |
rs397718730 | in-del | -/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714793 | AAATCTAAAGTTCCA[-/T]TTTTTTTTTTTTTTG | 9870 |
rs397821426 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713645 | ATTATTTTGTTTTTT[-/T]GCTTATTATCGTGTC | 9870 |
rs397853452 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690265 | CAAGACCCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 9870 |
rs397959057 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705056 | TGTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCGC | 9870 |
rs527273441 | snp | C/T | | | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673086 | CCTCACCTATGTTCT[C/T]ATGCAGGGAGCGGAT | 9870 |
rs527331305 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668981 | CTCCTGGGCTCAAGC[A/G]ATGTTCCAGCTTCAG | 9870 |
rs527339770 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707212 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCCAGG | 9870 |
rs527457978 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74693435 | TGAACCAAAAATGTA[C/G]CAGAAAGGGGGTTTA | 9870 |
rs527546937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693980 | CCAGGAGTTCAAGAC[C/G]AGCCTGGGCGACATA | 9870 |
rs527555729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686444 | CAAGGAAAAATGCAA[C/T]GTATGCTAACGTTCA | 9870 |
rs527632578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670679 | GTTGTCAGGTTCCCA[A/G]ATCAGTTTCATAATT | 9870 |
rs527737704 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74707899 | GAGGCGGAGCTTGCA[A/G]TGAGCCGAGATGGCG | 9870 |
rs527768087 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686260 | CTGGAAGATGAGCTC[A/G]GCAGAAAGACCAAGG | 9870 |
rs527796057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707394 | GAGGCCGGGCACAGT[A/G]GATCACACCGGTAAT | 9870 |
rs527869086 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74676870 | GGCGCAATCTCGGCT[C/G]ACTGCAAGCTCTGCC | 9870 |
rs527892921 | snp | C/T | 7.22348e-05 | 0.00600934 | intron-variant | AREL1 | GRCh38.p7 | 14:74684711 | AACACACAAACCGCC[C/T]GCCAGTTACACATTA | 9870 |
rs527900294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692390 | TGAAAAGGATTCCCC[A/G]GAAAAAAATCAAAGA | 9870 |
rs527933727 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714260 | GGAGTTCAAAACCAG[C/T]CTGGCCAACACGGTG | 9870 |
rs527992490 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704077 | ATTTCCCTAAGGACT[A/G]ACAATATTGAGTATT | 9870 |
rs528014636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677173 | AAGCTAGGTTTCCTC[C/T]CAATTCCTAGGGATA | 9870 |
rs528038328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666830 | GTTCAAGTAATTCTC[A/C]TGCCTCAGCTTCCCA | 9870 |
rs528199339 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692816 | TCAAGCGATCCTCCC[A/G]CCTCAGCCTCCCAAG | 9870 |
rs528209343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704303 | CATACGCCCAGGACA[C/T]GGCCTCATGAGGTCC | 9870 |
rs528296627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689048 | AGACAGGGTTTCACC[A/G]TGTCAGCCAGGCTGC | 9870 |
rs528300265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681502 | GATGGGGGGCAGGTA[C/T]GGTGGCTCATGCCTG | 9870 |
rs528416084 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661984 | CAGCATTATGTTTCC[C/T]AGGGTGGTGATAAAC | 9870 |
rs528472868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74695689 | ATTTACTAGTCTGTA[C/T]TGAAATTATTTGTTT | 9870 |
rs528508614 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686153 | TTGGCATTATGTAAT[C/T]AAAATGAACTCTGGG | 9870 |
rs528513631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703381 | AGGGAAACCACCCCA[A/T]GATTCAATTATCTCC | 9870 |
rs528535327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695270 | TTTTTGGTAGAGGCA[C/G]GGTTTCACCACGTTG | 9870 |
rs528560465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688389 | GAGAGCCACAGTCCA[A/G]TTATCATGAAGCTGG | 9870 |
rs528692404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672161 | CCAGGGATTCAATAA[A/C]AAGAAGTTTCTTCTG | 9870 |
rs528731016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74711062 | CATGGAGAAACCCCG[C/T]CTCTACTAAAAATAT | 9870 |
rs528734378 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74702749 | AAACTTTTATGCTCT[G/T]CTTCCCTTTTAAATG | 9870 |
rs528795412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710286 | CTACACTAATTTAGC[G/T]CCCTATTAGGTATTA | 9870 |
rs528836288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664707 | TTTGTGATCCGCCTG[C/T]CTCAGCCTCCCAAAG | 9870 |
rs528874790 | snp | C/G | 1.65666e-05 | 0.00287802 | intron-variant | AREL1 | GRCh38.p7 | 14:74672961 | GAGCCTCCTGGGGAA[C/G]AGCAAGATCCATCAT | 9870 |
rs528941846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712136 | AGACTTTGGAATCAC[A/G]AGACTCAAACAGACC | 9870 |
rs528998278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74665942 | CCTTCCTTTCTACTT[A/C]CTTCTACAAATTGTT | 9870 |
rs529044340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680463 | TTGCTGGTGGGAATG[C/T]AAAATGCTACAGCCA | 9870 |
rs529073765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74688316 | AGGCGTGAGCCACCA[C/T]GCCCGGCCCTGAGTA | 9870 |
rs529177376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74672484 | GCTCATGCCTGTAAT[C/T]CCAACACTTTGGGAG | 9870 |
rs529257040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694422 | AAAGTAGGAACAAAA[C/T]TGTTTATGTAGCACA | 9870 |
rs529292074 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74702699 | AAAAAATGGGTTTTT[C/G]TTTTCTATCGCCACT | 9870 |
rs529362050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695227 | TGGGACTACAGGTGC[A/G]TACTACTATGCCCAG | 9870 |
rs529402799 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699847 | GAAAAGAAACGAATC[C/T]GCTGCTCTTGGGGAG | 9870 |
rs529423446 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662347 | GTTTTGGCAATAAAG[A/T]TGGCTTGTAATATTC | 9870 |
rs529465373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74671548 | TCTGGATGTTAAAGA[C/T]AACACAAGAGCACTG | 9870 |
rs529527505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74679061 | CACGCCACCACACCC[A/G]GCTAATTTATAAATT | 9870 |
rs529551920 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74711047 | GACCAGTCTGACCAA[C/G]ATGGAGAAACCCCGT | 9870 |
rs529572995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709133 | AGTTAGTTAATAGCT[A/G]AAGTCATTTAAAAGG | 9870 |
rs529627500 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680214 | AAGAAAAGAAAAGAA[A/C]AGAGAAAAGAAAAGA | 9870 |
rs529644190 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663097 | AATGCCCGAAGGGAA[A/G]GTGCTTTTTCCAGTT | 9870 |
rs529679567 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700011 | TGTGCCAGGCCACAA[C/T]AGCCCAACCCACAGC | 9870 |
rs529754352 | snp | C/T | 0.00328676 | 0.0404052 | intron-variant, utr-variant-5-prime | AREL1 | GRCh38.p7 | 14:74698813 | AGGATGGCTTGCGCC[C/T]AGGAGTTCAAGACCA | 9870 |
rs529788757 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74691694 | TTGGCTCACATTACC[A/T]ACCAAAGGGGAAAAA | 9870 |
rs529900613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706058 | AAATCTAGAAAATAC[C/T]AGCTTCAGTTTCCTC | 9870 |
rs529926485 | snp | A/G | 4.17519e-05 | 0.00456883 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713068 | CCCGGCCTGGGAACC[A/G]GCTCGGGGGATTGCC | 9870 |
rs529926986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74667187 | AATGAATGGAGGAGC[A/G]ACAAAAGTGAAACCA | 9870 |
rs529928890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74675654 | AATACCAATTACACA[C/T]AGGTTCAAGCAGGGG | 9870 |
rs530031581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682981 | GTATTTCTTTACAGC[A/C]AGACAAAAGCAGCCA | 9870 |
rs530051451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74690012 | CAACACTTTGGGAGG[C/T]TGAGGTGGGAAGATC | 9870 |
rs530062284 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710329 | ATCAGAACACTCTCA[A/G]TAGAGGTTACAATAG | 9870 |
rs530107339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682237 | AAATTAAGGACTAGT[C/T]AAGCAAAGATACACA | 9870 |
rs530219063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704810 | GTGGTTTTTGTGTTC[C/T]ATTTTTTAAAACTCT | 9870 |
rs530219115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696958 | GACAAAGCAAGACTT[C/T]GTCTCAAAAAATAAA | 9870 |
rs530240452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683700 | CACAGAGAGAAACAA[A/T]TCCCCTCAATACTCT | 9870 |
rs530277467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704261 | GTCTCAGTTAATTTA[C/G]AAAGTTTATTTTGCC | 9870 |
rs530353159 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664384 | TTTCCCCATGCATCA[-/T]TTTTTTTTTCCCAGA | 9870 |
rs530392619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74689492 | CTAGGAAAAATCCTA[C/T]CCACTCTCTCCAAAA | 9870 |
rs530564693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74704955 | CTGCATTCCATTTAT[C/T]TCATAGTCATTAAGT | 9870 |
rs530605502 | snp | A/G | 0.000141553 | 0.00841168 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692318 | CGACTGCCAAAGGAC[A/G]CCCCAGGATCCTGTC | 9870 |
rs530727269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74666166 | CTTCAGTTAATAGAA[A/G]TAAGAATTGGGCAAG | 9870 |
rs530732235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682853 | GCCTTCCACCATGAG[A/T]GGAAGCTTCGCGAGG | 9870 |
rs530732307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673916 | TTTGGCAACGAATCC[C/T]GTGTACACTGTGAGA | 9870 |
rs530746702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667112 | TTATCCCTTAAGCTA[A/G]TATCTCTGCACTCTT | 9870 |
rs530783578 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713049 | ACCCCAGAGTTGGTC[C/T]CCACCCGGCCTGGGA | 9870 |
rs530920401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681634 | AAAAATTAGCTGGGC[A/G]TGGTGGCACGTGCCT | 9870 |
rs530932938 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685640 | TCAATGCCAACAGAC[A/T]GCCGAGGATCACAGC | 9870 |
rs530934268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688565 | ATTTAAAACTCAACA[A/G]ACCAATTACTACTTT | 9870 |
rs531030831 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74664649 | TATTGTTAGTAGAGT[C/T]GGGCTTTCACCATGT | 9870 |
rs531055673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711119 | GCCTGTAATCCCAGC[C/T]ACTCAGGAGGCTGAG | 9870 |
rs531058533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682055 | AAAAAGGCTGGTACA[G/T]GTAAGGGTATGAGCT | 9870 |
rs531080360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703969 | GCAATGCACAAGAGG[C/T]AGGTTGCTCTATATC | 9870 |
rs531216390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685689 | ACTTGTTTAGTTTTT[A/G]TCTCCAACTCTGCCT | 9870 |
rs531346767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693357 | GGAAAATCTGTGAAC[C/T]TTCAAAATAAAGTCA | 9870 |
rs531385678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700541 | TCCAGCATTTTGGGA[C/G]GCCAAGGCAGGTGGA | 9870 |
rs531463930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678360 | AAAATTAGCTAAGCA[C/T]GGTGGTGCACGCCTG | 9870 |
rs531471372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701284 | ATATATTAGTCCAAT[A/T]TCATGCTGCTGTTAA | 9870 |
rs531563411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668998 | TGTTCCAGCTTCAGC[A/G]CCCACTTCCTCCCAC | 9870 |
rs531616123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676835 | GGAGTCTCGCTCTTT[C/T]GCCCAGGCTGGAGTG | 9870 |
rs531656449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706824 | AGCATAGAGGGTATG[C/G]ATGGATACCTTAATC | 9870 |
rs531780440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683891 | CAAATTTAAAGGTAA[G/T]TTAGCCGGCAGCACT | 9870 |
rs531814859 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662388 | CTGCCCCATTGGGAA[C/T]GGTAGCTTGCAGCAA | 9870 |
rs531819192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74691022 | GTTGAGATTCAAGCC[A/G]GGCTGGGAAAGCCTA | 9870 |
rs531857695 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704415 | TACTGGCTCAGTCCA[A/G]AAAGGCGGGACAACT | 9870 |
rs531909284 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74676390 | GCCACTTTACTCCTT[A/G]CAAAGAGCTTTCCTA | 9870 |
rs531914089 | snp | C/T | 1.65877e-05 | 0.00287986 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684590 | CGGCGCTCGCGGTCC[C/T]CATTCTGGAGGAAGC | 9870 |
rs531918675 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707459 | CGAGGTCAGGAGATC[A/G]AGACCACCCTGGCTA | 9870 |
rs531934908 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710494 | CCCTCTGAACCTATA[C/T]ATAATACTAATGAGT | 9870 |
rs531998248 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696721 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAAGTG | 9870 |
rs532124479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74692578 | TATGTCTCCGGCTGA[A/G]AAGTGCCAGAGCTTC | 9870 |
rs532177107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74700387 | TATATTCTTTCTCTA[C/T]TCTTAACTGGCAATA | 9870 |
rs532198323 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662239 | AGGGCTTGTTCCTCA[C/T]GATCCCTGCGAACAG | 9870 |
rs532211727 | snp | C/T | 0.000166212 | 0.00911474 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685625 | AAACATCAGGTCCCG[C/T]CAATGCCAACAGACA | 9870 |
rs532259304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699721 | AAAACTGGTTATCAA[C/T]ATACATCATTTTGTT | 9870 |
rs532358693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668843 | GAAGCACATGCATCG[A/G]AAATATCTCTGGGCC | 9870 |
rs532391771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707166 | TGAGGTCAGAATTTC[A/G]AGACCAGCCTGGCCA | 9870 |
rs532472268 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | AREL1 | GRCh38.p7 | 14:74666750 | TTGAGACAGAGTCTT[-/A]ACTCTGTTGCCCAGG | 9870 |
rs532637460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697807 | CCTCAGTTCCATGAC[A/G]TACTACTCTTGAGCA | 9870 |
rs532762163 | in-del | -/A | 0.030278 | 0.119257 | intron-variant | AREL1 | GRCh38.p7 | 14:74680174 | AGAGCAAGGATGTCT[-/A]AAAAAAAAAAGAAAA | 9870 |
rs532822141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710330 | TCAGAACACTCTCAA[C/T]AGAGGTTACAATAGA | 9870 |
rs532826040 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74673410 | TTAAAATTATTTTAG[-/T]CACAGAGACTGCCTT | 9870 |
rs532941513 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686960 | AGTATCTCATCTCTT[A/C/G]GGACCCTATGCTGAA | 9870 |
rs532964570 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74695026 | AAAGAAAGAAAATGG[G/T]ATAAAGAAATTAAGA | 9870 |
rs533028479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74679549 | AAGCCAAAATGGGCC[A/G]GGCACGGTGGTTCAT | 9870 |
rs533195869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74694297 | ACAACAGACTATATA[C/T]GTAAGCTATAAGAGA | 9870 |
rs533211861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691515 | GTGAGGAATCTCATA[C/G]CAAGGCTAAAATTAG | 9870 |
rs533342732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711501 | TGAGCCGAGATTGCG[C/T]CACTGCACTCCAACC | 9870 |
rs533369933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677237 | CGGTGGCTCACACGT[A/G]TAATCCCAGCACTTT | 9870 |
rs533419104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74702179 | GCTCCACTAGACAGT[A/G]CCCCAGTGGGGACTC | 9870 |
rs533421643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74680910 | ACTTCTAGGCAGACA[C/T]AGTGGCTCATGCCTG | 9870 |
rs533568282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678111 | ATTCTAAAATTTAAA[C/T]GGAAAGGCAAAGGAA | 9870 |
rs533768069 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661888 | GGCTGCCGGAGGGGA[A/G]AATTCAGAAAAGCGA | 9870 |
rs533787091 | snp | C/T | 8.23703e-05 | 0.00641704 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713132 | CTTTGCCGGAAGCAG[C/T]ATGTGAATGACGTAG | 9870 |
rs533909512 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662440 | TTGGGAAGTCAATGA[A/G]ATTTTGAATCTTGAA | 9870 |
rs533982891 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692118 | ACTTTTGGCCCCTTT[C/T]ACCTTGTCTTCCAAC | 9870 |
rs534059434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697400 | CTATTCAATTTTCAA[A/T]AAGTGCACAGGTTAG | 9870 |
rs534103630 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705082 | TTCGCTCTTGTTGCC[A/C]AGGCTGGAGTGCAAT | 9870 |
rs534107459 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661454 | CAGAAGGGTAGCTGG[-/C]CCCCCCAAGTACCTG | 9870 |
rs534109352 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700955 | AGGGGGACAGACCCA[C/T]TAATGAGCACAAGAT | 9870 |
rs534214295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706533 | GCCACAGAAATGGCA[C/G]CCTAAGATAGCTGGA | 9870 |
rs534225358 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714335 | GAGAATAGTCGTTAA[A/T]ACCTTCAGAATTATT | 9870 |
rs534241068 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664219 | AACAGTTTGACAAGC[A/C]CTTCAAGAATTTACA | 9870 |
rs534247032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669237 | GTGTTAAAATAGGAA[C/T]CACCTACATCACTAC | 9870 |
rs534499486 | snp | A/C/T | 3.17093e-05 | 0.00398166 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714982 | TTTCCTTTAAAACCA[A/C/T]AGACCTCTTAGAAAT | 9870 |
rs534527484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672508 | TTGGGAGGCTGAGGC[C/G]GGTGTATCACTTGAG | 9870 |
rs534605456 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711438 | GTCCCAGCTACTCGG[C/G]AGGCTGAGGCAGGAG | 9870 |
rs534781659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680593 | AAAACCTGTAAGTGA[A/G]TATTTATAGCAGCTT | 9870 |
rs534928619 | in-del | -/AAAC | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74709004 | AACTGCAATAAGGTT[-/AAAC]AACCTCAAAAGTTTG | 9870 |
rs534937246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709500 | TACAAGTCTTTCTGT[A/G]ATACAGGACTGTGGT | 9870 |
rs534994055 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74687995 | CATCCTAAAATAATT[C/T]GTCCAACAAATACTG | 9870 |
rs535001868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74679789 | GCTGAGATTGTGCCA[C/T]TGCACTCTAGCTTGG | 9870 |
rs535025445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702297 | CCTGAACATTCAGGA[A/G]TTTCCATACATCCTC | 9870 |
rs535059664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687248 | GGAATAAAAGCAGTG[C/T]CAAATGTATGGCTTG | 9870 |
rs535117829 | snp | A/G | 0.000364299 | 0.0134914 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663967 | TGAGGGACAGAGGGC[A/G]GCAAAGCCTCCAGGT | 9870 |
rs535130231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74695435 | CAACCCTGTGATCAG[A/C]TATTTGATTATTAAA | 9870 |
rs535189842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702959 | TCACCATTTTGTTCA[A/C]AGTCATTCAACAAGT | 9870 |
rs535239353 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678438 | AGGAGGCCAAGGCTG[C/T]AGTGAATCATGATCG | 9870 |
rs535270007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671143 | TCTCAAGGTAACCAC[A/G]GTTCAAACACTTAGA | 9870 |
rs535271333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679711 | CAGATGCCTGTAATC[C/T]CAGCTACTTGGGAGG | 9870 |
rs535277229 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661458 | AAGGGTAGCTGGCCC[C/T]CCAAGTACCTGGGTC | 9870 |
rs535297501 | snp | A/C | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712541 | CAAGGCTTCACAATA[A/C]ATGTGCATTGTATCT | 9870 |
rs535370278 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682189 | GCTTGAGAGCCACTT[C/T]GTCCAGAGCCTTACT | 9870 |
rs535389344 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74697882 | ACTGTACCTCATTCT[A/G]TAACTCCCAGATTTG | 9870 |
rs535488263 | in-del | -/AAC | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74705502 | GATACTGGTTCTTAA[-/AAC]AACAACTAAATTCCA | 9870 |
rs535520713 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74678811 | TTTGGGAAAAAAAGA[A/G]AACATCTTCAGGATC | 9870 |
rs535597556 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695732 | CTCCTAATAGATTGC[A/G]GACTCCCCAAGGAAC | 9870 |
rs535710743 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673839 | CCTGTTTCTGTAGGC[A/T]TGCGTCCTTCCAGAA | 9870 |
rs535729010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709731 | GGAGAAAAAAAGTCC[C/T]ATCATGTAAGTCAGA | 9870 |
rs535736373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692988 | TGCTGGGATTACAGG[C/T]GTGAGTCCATTCTTC | 9870 |
rs535766969 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663307 | GTCTGGTCAAGTAGT[A/G]AGGGCCAAAGAGGGT | 9870 |
rs535827049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686629 | AGACAGCTAAAAATT[C/T]CTAGGCTCAGATCTG | 9870 |
rs535892323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693640 | ATGAGGAAACTGGGA[C/T]ACAGAAAGGTTAAAG | 9870 |
rs535908001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74690486 | TCCTCAACCTAAAAG[C/T]TGCCAATTTAATTCA | 9870 |
rs536064373 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661837 | GACAGGTCTAGCCAA[A/G]ACAATCAACTCAATC | 9870 |
rs536090548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707560 | CAGCACTTTGGGAGG[C/T]CCAGGCAGGTGGGTC | 9870 |
rs536115291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701556 | ATCTCCCACTGGATC[A/C]CTCCCATAACACATG | 9870 |
rs536178565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700875 | AAGATGTTTTTTAAC[C/T]GAGAGAGAAAAAGGA | 9870 |
rs536178655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708196 | CAGGAATACTCTGTA[C/T]TATCTTTGCAACTTT | 9870 |
rs536320454 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74684021 | GGAAATTTTTTCTGT[A/T]AAGTGCCAGAGAGTA | 9870 |
rs536413575 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694082 | CTTGGAGGCTGAGGT[A/G]GGGGTTGGCTTGAGC | 9870 |
rs536476412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74704531 | ATATGCATCTATCTC[A/G]GTAGGCAGGGGATGA | 9870 |
rs536507725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681639 | TTAGCTGGGCGTGGT[A/G]GCACGTGCCTGTAAT | 9870 |
rs536533317 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705282 | GACCTCAGGTGATTC[A/G]CCCACCTCAGCCTCC | 9870 |
rs536626629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689753 | AGGCATGCACCACCA[C/T]GCCTGGCTAATTTTG | 9870 |
rs536635486 | snp | C/T | 1.97783e-05 | 0.00314464 | intron-variant | AREL1 | GRCh38.p7 | 14:74674151 | GAAGTGAATGATAAA[C/T]AAAAAGGCTCTATTT | 9870 |
rs536748212 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686682 | TTCAGGGTGTGTTTT[C/T]ACATCTGATTGTGCT | 9870 |
rs536771387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666236 | CCTTCCTCCCTAAAG[A/C]AACGTTTGCAGAAAG | 9870 |
rs536888713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688126 | TGCCTCCCGGGTTCG[C/T]GCCATTCTCCTGCCT | 9870 |
rs537014858 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683924 | CAATGAGTGAACTAA[A/C]GCGTTACCAGACAAA | 9870 |
rs537099452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74677791 | CAGGCGTAAGCCACG[A/G]TGCCCAGCTAACCCT | 9870 |
rs537119396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74690426 | TAGATAGAGTTTGAA[A/C]GGATTTCTCTAACAG | 9870 |
rs537229572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695378 | AGCCACCACACCCAG[A/C]CTGAACTTTTATTTC | 9870 |
rs537279350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711664 | GTAGTCTGGTTTACA[C/G]TCTTCTAGGGACCTC | 9870 |
rs537299245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704422 | TCAGTCCAGAAAGGC[A/G]GGACAACTTGGAGTA | 9870 |
rs537312001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696342 | TCTAGTTTCAACTAT[A/G]ACTTGATGGCTTTAT | 9870 |
rs537362781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712447 | AACCACTGGAATACA[C/T]AGCAGGTACTCAAAG | 9870 |
rs537447218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672628 | TATAGTCCCAGCTAT[C/T]TGGGAGGCTGAGTTG | 9870 |
rs537569532 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661084 | ACAGCAATCAGGGAA[C/G]GGTGAAAGGGCAAGA | 9870 |
rs537579875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664142 | AGATCCCTGGGGAAG[A/G]AACAAGATACACTAA | 9870 |
rs537624983 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74687379 | ACAATCCCAGGACTG[A/C]AAACTGTGTGACCTA | 9870 |
rs537709547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688095 | CAGTGGTGTGATCTC[A/G]GCTCACTGAAAGCTC | 9870 |
rs537826366 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698076 | TAAAGATAAAACATG[A/G]ATATGTTGAATATAT | 9870 |
rs537829132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669539 | TTTGGGTGTTTAATA[A/G]ACAACACAAATATGG | 9870 |
rs537831188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677400 | ACTCAGGAAGCTAAG[A/G]CAAGAGGATCACTTT | 9870 |
rs537968123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74670261 | CCATCCAAATGTTAG[C/T]TTTTTGGTAGCCACC | 9870 |
rs537973422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74706204 | TGGACCACTGAATCT[C/T]GGCTATAACAGGAAG | 9870 |
rs538039671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74675363 | TTAAAAAGAAACTAA[C/T]ACAAAGTGCTTCTTA | 9870 |
rs538040717 | snp | C/G | 3.35734e-05 | 0.00409702 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669978 | AGTCCTATGATTTGG[C/G]CCAGGAAAGAGCGGG | 9870 |
rs538053779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683143 | GATGATGGCTGCATT[C/T]AAAGAACCATTAAAC | 9870 |
rs538116165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684911 | CTGCCTATTTTGGTA[A/C]ATAAAGTTCCATTGG | 9870 |
rs538142897 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675640 | GGTTTCTGCTACCAA[A/C]TACCAATTACACACA | 9870 |
rs538186826 | snp | C/T | 1.66225e-05 | 0.00288287 | missense | AREL1 | GRCh38.p7 | 14:74667476 | CCACCTTTTAGGAAA[C/T]GTTCCACCTCCTCTT | 9870 |
rs538212992 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696736 | TTGGGAGGCCAAAGT[A/G]GGCAGATCACCTGAG | 9870 |
rs538240452 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707959 | GAGACCTTCGCCTCA[-/G]AAAAAAAAAAAAAAA | 9870 |
rs538270486 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714087 | CCTAGTATGAAGAGG[A/G]TCAAAGCGGTGTCCC | 9870 |
rs538470436 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665427 | CCCTAAGAACTGCTA[C/T]TATGGATTATTTTTA | 9870 |
rs538486692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698298 | CCATCCTAGATATCT[A/G]TATTTATTTTCTCTT | 9870 |
rs538618414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684852 | AGAAAGGAACTTCTA[C/T]ACCAGGGGTCAGTAA | 9870 |
rs538675488 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693505 | GAAGAGACTACTAAT[C/T]AGTAAATGAAGAGAC | 9870 |
rs538681563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684213 | TAATACTTACTCTTT[C/T]CTGTAATATTTTTCT | 9870 |
rs538748441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705145 | TCCAGGTTCAAGCGA[A/T]TCTCCTGCCTCGGCC | 9870 |
rs538765145 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706011 | AAAAGAGAAAACTGG[C/T]TCATCCATGTCACTG | 9870 |
rs538840884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682314 | GGGACCCCAGGTCCT[A/G]TTATTTCTGTGGATA | 9870 |
rs538934671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74674277 | AAATAAATACATTAA[C/T]TCTCTATTTAAAAAG | 9870 |
rs539029846 | snp | C/G | 0.000383484 | 0.0138418 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684646 | GAGGAACTTAATTGT[C/G]AAGAAGAATGCAACC | 9870 |
rs539069591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671759 | CTTTTGTTTTAAACA[A/G]TCCTTGTTTTAGCAA | 9870 |
rs539166724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74709594 | TAATCTATCTCTGAG[G/T]TATTCTTACAAACCA | 9870 |
rs539230828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678682 | ATGATGCTGGAGTAA[A/G]GACATGTATAAGCAA | 9870 |
rs539255138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677641 | CTGAGTAGCTGGGAC[C/T]ACAGGCACCCGCCAC | 9870 |
rs539266333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681685 | TGAGGCAGGAGAATC[C/T]ACTGAACCAGGGAGT | 9870 |
rs539301647 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683357 | ACCAAGCTTCACTGT[C/G]ATTTCATAACGCCCA | 9870 |
rs539426580 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662668 | CATCCCTAGTGTCCT[A/G]ACGCCAAGGACCTGT | 9870 |
rs539452057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689651 | TGCCCAGGCTGGAGT[A/G]CAATGGCGTGATCTC | 9870 |
rs539495003 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708701 | AGTAACAAGCTGCAC[C/T]GAAATAAATGCCTTC | 9870 |
rs539500767 | in-del | -/CAAAA | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74700778 | AGCGAGAGTCCCTCT[-/CAAAA]CAAAACAAAACAAAA | 9870 |
rs539588930 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687395 | AAACTGTGTGACCTA[C/T]CTAGGCTTCAGAATC | 9870 |
rs539604540 | snp | A/C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686315 | TCTCATCCTCAGTCA[A/C/T]GCCTGTCAAGGTAGG | 9870 |
rs539639638 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660987 | TAAAGACTGATTAAC[C/T]GGTTCCTTCTTCAGA | 9870 |
rs539704688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700046 | GAGGAAGATGGCTTC[A/C]ATCTACCTGAAGGAC | 9870 |
rs539708634 | snp | C/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661137 | GTGTACACTCTACCC[C/T]GAGCCGACCACTTCA | 9870 |
rs539803493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692867 | CACTACCACACCTGG[C/T]TAATTTTTTATTTGT | 9870 |
rs539867828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700760 | ACTCCAGTCTGGGCG[A/G]CAGAGCGAGAGTCCC | 9870 |
rs539887374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670943 | TGTTTATTGAGTCAT[C/G]ATTTTATACTCTCCA | 9870 |
rs539957686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707622 | AACATGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9870 |
rs540024821 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702491 | AGGGCACCAAGTCCC[C/T]ACACTGCACACAGCA | 9870 |
rs540098197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707445 | AGGTGGGCGGATTAC[A/G]AGGTCAGGAGATCGA | 9870 |
rs540135099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706740 | TTAGAAACATAAAAG[C/T]TTAGTAAAGAAGACA | 9870 |
rs540158396 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74706985 | TCAGGGTCAATGACT[C/G]TCTTCAACACTCGTC | 9870 |
rs540193324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707134 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 9870 |
rs540198939 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714628 | TATAATCAGCTTTTA[C/T]TTACTCATTAACAAT | 9870 |
rs540336949 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694441 | TTATGTAGCACAAGT[C/G]CAAATTTAGAAACAT | 9870 |
rs540343294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691390 | GCTCTTAACCTCTAC[A/G]GTGAATCATGAAAAA | 9870 |
rs540394312 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662004 | TGGTGATAAACCTTC[C/T]GGTACATATCCCATG | 9870 |
rs540441108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704822 | TTCTATTTTTTAAAA[C/T]TCTGCCTAGCTCAAG | 9870 |
rs540505319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669558 | ACACAAATATGGAAC[A/T]TTTCCACCACTGCAG | 9870 |
rs540532139 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702810 | ATTCAAAGTTCCACA[A/G]ATTTCTAGGGCAGGA | 9870 |
rs540537620 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666226 | TAAAAGAAAACCTTC[C/T]TCCCTAAAGAAACGT | 9870 |
rs540655920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695493 | CTTTACTATCCCTAC[C/T]GTGAGCTACCATGCT | 9870 |
rs540727291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681043 | ATCAAAAAATTAACC[A/G]AGCGTGGTGGTGCAC | 9870 |
rs540762551 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74666846 | TGCCTCAGCTTCCCA[A/G]GTAGCTGGGATTACA | 9870 |
rs540790044 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713301 | TCACATTATCCTAGC[A/T]TATTTTCATTCTGGT | 9870 |
rs540801612 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74686982 | TATGCTGAATTAGCT[-/G]GGGACCCAACAGCTA | 9870 |
rs540833827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709815 | ATAACTTTCTAACAT[C/T]GAAATACAAGATGTT | 9870 |
rs540838354 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663496 | CATGACAGAATGAAG[A/G]GCTCAGCTTACATAC | 9870 |
rs540920005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694970 | CTCCAGCCTGGGCGA[C/T]AGAGTGAGACTCTGT | 9870 |
rs540926978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705524 | ACTAAATTCCACAAC[C/G]CAGAACATGCACCTT | 9870 |
rs540946718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694006 | ACATAACAAAACCCC[A/G]TCTCTACAAAAAATA | 9870 |
rs541050344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671269 | CCCTTTTCCTTGGGG[A/G]AAAAAAAACCTAGGT | 9870 |
rs541095967 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662881 | TCAGTGGCCCAAGCC[A/G]GCCATACTTCAGTGC | 9870 |
rs541113667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678905 | ATTTCTTTCTTTCTT[C/T]TTTGAGACAGGGTCT | 9870 |
rs541139765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680280 | ACCAAAGGATACATA[C/G]ATGACAGACAGGCAC | 9870 |
rs541252818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702111 | GCACATGGTACAAAC[C/T]GTCAGTGAATCTACC | 9870 |
rs541449643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74693951 | GGAGGCCAAGGCAGG[C/T]GGATCACTTGAGCCC | 9870 |
rs541468157 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714427 | AATTTCTTTCTAGTT[A/G]AGGGTTAAGTTCTGT | 9870 |
rs541518693 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709262 | GGCAACATAGCAAGA[G/T]CTAATAAATAATAAA | 9870 |
rs541608320 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680662 | CCTTTAACAGATGAA[C/T]AGTTAAACAAACTGG | 9870 |
rs541653612 | snp | A/G | 1.7051e-05 | 0.0029198 | intron-variant | AREL1 | GRCh38.p7 | 14:74676099 | AACAGGCAAAGAAAC[A/G]GCTGAAGAACAGCAC | 9870 |
rs541668631 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74677953 | AATAAAACAAAAAAA[A/C]CAACAAACAACTAAA | 9870 |
rs541674286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74693125 | GACAAGTGAGATGAA[C/T]GCACAGCCAGAACCA | 9870 |
rs541712058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701858 | CTGTTCCAAATGGGA[G/T]AAATTGGCCAAAACA | 9870 |
rs541722262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74701291 | AGTCCAATTTCATGC[C/T]GCTGTTAAAGACGTA | 9870 |
rs541728592 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74678995 | CCTGGGCTTGTTATC[-/CA]CTACCACCTCACTTC | 9870 |
rs541753790 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74684349 | AGTTCCTGGAGGGAG[C/G/T]TGAAAAACAAGAGAA | 9870 |
rs541760573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708886 | AAACCCTATCTTGTA[A/G]AACAGTCTTCAAAAG | 9870 |
rs541797898 | snp | A/C | 0.000464624 | 0.0152347 | intron-variant | AREL1 | GRCh38.p7 | 14:74669934 | AGTAGGAAATGCACA[A/C]CCAAGATGTTACCTT | 9870 |
rs542337660 | snp | A/C | 0.0017206 | 0.0292804 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712972 | GAAGTTCCACCTCCG[A/C]TGTCCTGGGAAGGGG | 9870 |
rs542517449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74681825 | GGGATAGGTGTGGCT[A/G]TAAAAGGGCAACATA | 9870 |
rs542571230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74688993 | AGGTGCCCACCACCA[C/T]GCCAGGCTAATTTTT | 9870 |
rs542572462 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74707719 | GAAAGGTGTGAACCC[A/G]GGAGGCGGAGCTTGC | 9870 |
rs542618198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710995 | CCAGCACTTTGGGAG[A/G]CCAAGGTGGGCGGAT | 9870 |
rs542741475 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693782 | ACCAAGGAAGAAAGC[A/T]CAAAATGCTAAAAGA | 9870 |
rs542850145 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704104 | TATTTTTTTCATGTG[C/T]TTATTGGTTATTTGT | 9870 |
rs542902177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680238 | GAAAAGAAAAGAAAA[C/T]GGACAAAAGACACGA | 9870 |
rs543045698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664186 | CCCAGTTACCGTTCT[A/G]TGAGGACACAGGGTA | 9870 |
rs543131251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703900 | ATCTACTTAACTTAC[A/G]AGAAACTGCCAAACC | 9870 |
rs543144369 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74710816 | AGAAAGGAGAAGCAG[-/A]AAAAGTTTACACCCA | 9870 |
rs543145251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703351 | AGACTTATTCACTAC[A/C]ATGAGAACAGTATGA | 9870 |
rs543230644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74672133 | TTCCTTTTAATTCAA[C/T]AAGCGCTCTATTCCA | 9870 |
rs543445945 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663590 | GGTGACAAAATCCTC[C/T]AGACACAGGGGAGCA | 9870 |
rs543451776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688886 | CTGTTGCCTAGGATG[C/G]AGTGCAGTGGCATAA | 9870 |
rs543456111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672105 | ATCAGACCAAAGTGA[A/C]AACAAAAATCATTTC | 9870 |
rs543510076 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74693107 | GTCTGGAGCAACCAC[-/AA]AGACAAGTGAGATGA | 9870 |
rs543934233 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74702656 | CTTTATTTATGCAAA[A/T]TTCTGTAGCCAGTTT | 9870 |
rs543944590 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74709916 | AGACCAATTAGTGAA[G/T]GGAATGAAGTCCAAG | 9870 |
rs543985658 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710630 | CTCTACACATGAATG[A/G]CAGCTTGACAGAGAC | 9870 |
rs544060194 | snp | C/T | 3.41326e-05 | 0.004131 | intron-variant | AREL1 | GRCh38.p7 | 14:74671390 | TCAAAAAGATGAATA[C/T]AAAATTTCAAAACTG | 9870 |
rs544084693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74676946 | GGACTATAGGTGCCC[A/G]CCACCATGCCCAGAG | 9870 |
rs544095110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680154 | CACTGTACACCAGCC[G/T]GGGCAAGAGCAAGGA | 9870 |
rs544116989 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713267 | AGAAGGAGGTAGTCA[C/G]ACCGTGGCCAAATTT | 9870 |
rs544140501 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74668081 | CACAGTTTGATACTT[A/G]AAGATCCTGGATTCT | 9870 |
rs544159039 | snp | C/T | 1.78118e-05 | 0.00298422 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713464 | TTCCAACTTTTTTAA[C/T]TCTAAAATTTCTGTT | 9870 |
rs544160989 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714431 | TCTTTCTAGTTAAGG[G/T]TTAAGTTCTGTATAT | 9870 |
rs544316808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697588 | TTTATACAGTTGTCT[A/G]TTTCTGCTATTGTGG | 9870 |
rs544327364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706686 | AAGCAATATGTTGGA[A/C]CCTAAAGATTCCAGA | 9870 |
rs544398246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74675633 | ACTTTGTGGTTTCTG[C/T]TACCAAATACCAATT | 9870 |
rs544458557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683633 | AGCTGGCAGAGACCA[A/C]ACCAGTAAATCCCAG | 9870 |
rs544484292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74665842 | GCCCAAACTGAGCCT[A/G]AGAAGCCTTGGCTCC | 9870 |
rs544514304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712902 | AAGGCAGGTCTTCTG[A/G]GCTCTGCCTAAGGCT | 9870 |
rs544514314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704099 | TTGAGTATTTTTTTC[A/C]TGTGTTTATTGGTTA | 9870 |
rs544669092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682876 | TCGCGAGGCCTCACC[A/G]GAAGCAGATGCTGGT | 9870 |
rs544755383 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702517 | CAGCAGGGGGGACCT[C/G]GGCCCTGCCTTCAAA | 9870 |
rs544785503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74666574 | TAGCCCATGAGGGCT[A/G]GAACTTTGTCTTATT | 9870 |
rs544962591 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692038 | CTCAGTCTGTTACCT[G/T]ACCTTTAAACGAGGG | 9870 |
rs545106645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703937 | CAAAGCGGCTGGACC[A/G]CTTTGCATTTCCACC | 9870 |
rs545136856 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713372 | TACAGAGTGGGGAAG[A/G]GGGTCTGGGTTATTT | 9870 |
rs545190521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696542 | TCTACTTCTAAAGTG[C/G]TATTCTAAAAAGCTG | 9870 |
rs545204403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682806 | TCTCTCTTGCTCCCT[C/T]TCTCACCATTAGGCA | 9870 |
rs545237302 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714610 | ACTAAAAAATAAATA[C/T]AGTATAATCAGCTTT | 9870 |
rs545267672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689904 | CCCGGCCTAGCACTT[C/T]TATTCTTTTAGTCTC | 9870 |
rs545279967 | snp | A/G | 0.00220149 | 0.0331044 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683500 | GTCCCACAGGCCGAT[A/G]TGCAGGGAAAGGCTG | 9870 |
rs545375310 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667004 | GGATTACAGAAGTGA[A/G]CCACCATGCCCGGCC | 9870 |
rs545504511 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74679056 | AGGTGCACGCCACCA[C/G]ACCCAGCTAATTTAT | 9870 |
rs545505536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704649 | TTATTTTCCTTTCAC[A/G]TAAATATAAGTCCTT | 9870 |
rs545516333 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709394 | TACTCTGACCTGGAC[A/C]ACTTACAGAAAGATG | 9870 |
rs545567184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673515 | AATGGCAATACGGTG[A/T]TATATTAAATAGCAA | 9870 |
rs545600245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701763 | CAAGGCAAGTCCCTT[C/T]TGCCTATGACCCTGT | 9870 |
rs545692567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707813 | AAAAAAAAAATTAGA[C/T]GGGTATGGTGGCGGG | 9870 |
rs545718538 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672031 | CATTCCTGGGGAATG[C/T]AAGAACTATGCCAGT | 9870 |
rs545774630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685254 | AATCCCCACCAGAGT[C/T]AGCAGTTCCCTTTTC | 9870 |
rs545808632 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662103 | GAGGATCCTGGGGTA[C/T]AGAGACCCTGATGCT | 9870 |
rs545820413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701038 | GGTCCAACATAGACC[C/T]TCATTAGTCACATTG | 9870 |
rs545837241 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74678997 | CTGGGCTTGTTATCC[C/T]ACCACCTCACTTCTC | 9870 |
rs545857611 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74676827 | TTTGAGATGGAGTCT[C/G]GCTCTTTCGCCCAGG | 9870 |
rs545921243 | snp | A/G | 0.000843882 | 0.0205239 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692153 | ACATGAAAGAAAAAC[A/G]CCACAAGGTCAACAG | 9870 |
rs545985317 | snp | C/T | 1.65671e-05 | 0.00287807 | missense, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669719 | TCACTCATGTCATTG[C/T]TGAGGATAAAACAAA | 9870 |
rs546047314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691480 | AAACAAAGTATGAGA[A/G]AACACTATCCAATCT | 9870 |
rs546246580 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74677049 | CCTGATCCGCCCGCC[C/T]TGGCCTCCCAAAGTG | 9870 |
rs546432560 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668317 | GGAATATTTGTGTAG[A/C]GTGACCAAGGTTGTC | 9870 |
rs546448529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705016 | GCTGCACATTACCAT[A/G]CACTATTTAAGTTAC | 9870 |
rs546495851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699432 | GAGACAGCACACAAG[C/T]GAGAGAGCCCTGCAA | 9870 |
rs546580723 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693147 | CCAGAACCAGGTTAC[A/G]GACAGCCTTATATGC | 9870 |
rs546586831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699606 | TATTTTAATATGTAT[A/G]TTATGTTCTGGTCTT | 9870 |
rs546587187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691211 | TGCAGTCCCAGTTAC[C/T]TGGGAGGCTGAGGCG | 9870 |
rs546623379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688169 | TAGCTGGCATTACAG[A/G]TGCCTGCCACCATGC | 9870 |
rs546715992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696282 | CAGTTCTACCATCTC[C/T]TCTTAGGAAAAGAAT | 9870 |
rs546722177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691712 | CAAAGGGGAAAAATA[A/C]TTCAAAATATCTGTC | 9870 |
rs546774095 | in-del | -/CT/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665270 | TATTTCTTTCTTTTC[-/CT/T]TTTTTTTTTTTTTTT | 9870 |
rs546823171 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695304 | AGGCTGGTCTTGAAC[C/T]CCTGACCACAGGTGA | 9870 |
rs546862328 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74668239 | AACAGAATTGGTATC[A/C]CCCAATAAACTCCTA | 9870 |
rs546881406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706081 | GTTTCCTCTTCCCTC[C/T]TATCTTGATGTGTTT | 9870 |
rs546882129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74690065 | CCAGTCTGGGCAATA[C/T]AGTGGGACCTCACCT | 9870 |
rs546897032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698948 | AGGATCATTTGAGCC[A/C]AGGAGGGTGAGGCTG | 9870 |
rs546973806 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74682275 | AGGCCCCACTCAGTA[A/C]GGTTTCACTTCAAAA | 9870 |
rs547222553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693444 | AATGTAGCAGAAAGG[A/G]GGTTTATGGCAATGC | 9870 |
rs547308457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686502 | ACAGGCTGTATATGC[C/T]ATTTTACAATGCATG | 9870 |
rs547412292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671008 | GTTGCGACTCATCTA[A/C]ACTGTGGTCCTTTAG | 9870 |
rs547426675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672215 | ACATGGGAGTTCCAA[A/G]GGACCCATTCAGTAG | 9870 |
rs547473623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663196 | CCATTGTGCAGCGGG[A/G]CTGCTCCTATGGGCC | 9870 |
rs547480629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692804 | GACCTCCTGGGCTCA[A/G]GCGATCCTCCCGCCT | 9870 |
rs547570893 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74701432 | GCAGCAGGCAAGAGA[C/G]AATGAGAGCCAAGCG | 9870 |
rs547582962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74707973 | AGAAAAAAAAAAAAA[A/G]AAAGAAATTACACAT | 9870 |
rs547626011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678550 | AAGATTCTGTGGTAC[C/T]GGAGGAGGGATAGGT | 9870 |
rs547639633 | in-del | -/A | 0.247053 | 0.249983 | intron-variant | AREL1 | GRCh38.p7 | 14:74698859 | TGAGATCCCATCTCT[-/A]AAAAAAAAAAAAAAA | 9870 |
rs547645061 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660864 | TTATCAAAGTGTTAA[C/T]GGTGATTACCTCTGG | 9870 |
rs547704080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669246 | TAGGAATCACCTACA[C/T]CACTACTGCAAATGT | 9870 |
rs547740809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707404 | ACAGTGGATCACACC[A/G]GTAATCCCAGCACTT | 9870 |
rs547771867 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708002 | ATGATCTAACTGGAA[C/T]GTGGTATTCTAGATT | 9870 |
rs547794931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677215 | CAAGAGGAAGAGAGG[C/T]CAGGTGCGGTGGCTC | 9870 |
rs547846080 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709155 | TTTAAAAGGTAAAAC[A/G]GTCAGGCACAGTGGC | 9870 |
rs547878527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74700672 | GTATTCCCAGCTACT[A/G]GGGAAGCTGAGGCAG | 9870 |
rs547907618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74674465 | AAATTAGCTGGGTGC[A/G]GTAGCTCATGCCTGT | 9870 |
rs547907674 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711187 | AGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAG | 9870 |
rs547944901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700637 | CAAAAAAAATTAGCC[A/G]GGCATGGTGGCACAC | 9870 |
rs547949961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688768 | TTCTGAATTTGCCTT[C/T]GTTCTACAAATTCCC | 9870 |
rs548058350 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679677 | ACTAAAAACACAAAA[A/G]ACTAGCCAGGCATGA | 9870 |
rs548157503 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74715011 | ATCCAGGCTTTCCCT[C/G]AGCTGGTTTGCTAAC | 9870 |
rs548225532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74669019 | TTCCTCCCACACTAC[C/T]CCAGTAGCTAGGACC | 9870 |
rs548241712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677541 | AGACAGAGTCACGCT[C/G]TGTCACCCAAGCTGG | 9870 |
rs548251557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707336 | TGGTGCCATTGCACT[C/T]CAGCCTGGGTGACAA | 9870 |
rs548268009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670983 | TATTGTACTACTCTG[A/G]TGTTTCTCCGTTGCG | 9870 |
rs548357349 | snp | A/C | 0.0174175 | 0.0916809 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661618 | TAGAAAAAAAAAAAA[A/C]AAAACAGTAAAAGAA | 9870 |
rs548435897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676858 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 9870 |
rs548455173 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74685704 | GTCTCCAACTCTGCC[G/T]CATAGCTATCTCAGA | 9870 |
rs548467990 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700209 | CATTGTATAAAGTGC[G/T]ACATCTATATTATCT | 9870 |
rs548614621 | snp | C/T | 3.32403e-05 | 0.00407664 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684625 | TACACGTGCGGCAAG[C/T]TCAAAGAGGAACTTA | 9870 |
rs548617996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664747 | TACAGGCATGAGCCA[C/T]TGCGCCCGGCCTCCT | 9870 |
rs548648939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74696109 | AGCTGAGTAGTTGCA[A/G]CAGAGACATATGGCC | 9870 |
rs548655898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711335 | ACCTGAGGTCAGGAG[C/T]TTGAGACCAGCCTTG | 9870 |
rs548710026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703661 | CATGTTGTTACACAT[G/T]TCGGTAGTTCACTCC | 9870 |
rs548799859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683943 | TTACCAGACAAAGGT[A/T]GGAGGGGTTCAGACT | 9870 |
rs548819538 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681434 | TTCAAATGACAAAAT[C/T]ATAGAAATGGGGAAT | 9870 |
rs548825422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673007 | AGCCATCTGTGTAGT[C/T]CTGCCTCTCCACCCT | 9870 |
rs548884827 | in-del | -/A | 0.375 | 0.216506 | intron-variant | AREL1 | GRCh38.p7 | 14:74694991 | GAGACTCTGTCTCGG[-/A]AAAAAAAAAAAAAAA | 9870 |
rs548886377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672486 | TCATGCCTGTAATCC[C/T]AACACTTTGGGAGGC | 9870 |
rs549093180 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689681 | CAGCTCACCGCAACC[C/T]CTACCTCTGGGTTCA | 9870 |
rs549102915 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712148 | CACGAGACTCAAACA[C/G]ACCCCTGAACAAAGT | 9870 |
rs549296165 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663102 | CCGAAGGGAAAGTGC[C/T]TTTTCCAGTTCTGAC | 9870 |
rs549364583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694523 | CATCTCTTGGTATAC[A/G]GAATTATAAATAATT | 9870 |
rs549366656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702709 | TTTTTCTTTTCTATC[A/G]CCACTGTCAGGCTGC | 9870 |
rs549442596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711139 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTAAACC | 9870 |
rs549444288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702841 | GCAAAATGATTCCAG[C/T]CTCCTTGCTAAAGCA | 9870 |
rs549453379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74709167 | AACGGTCAGGCACAG[C/T]GGCTCATGCCTCTTC | 9870 |
rs549460369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687127 | CAGCGGGATGCCATT[C/T]GATCTGACCCTAGAT | 9870 |
rs549505659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74710421 | CATTACCAGAAGAGC[A/G]TTTTTCTGTCAGTGC | 9870 |
rs549509488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708343 | TTCAGGTAATGCCAG[A/C]CTAAAACTTTTTAAA | 9870 |
rs549601828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687014 | CATCTCAAAAATCTG[C/T]TACGATCTCTCAAAA | 9870 |
rs549647902 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74671560 | AGACAACACAAGAGC[A/G]CTGCCATTGTCTGCT | 9870 |
rs549678765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702238 | CCCCAACATTGCCCT[A/G]GCAGAGGTTCTCCAT | 9870 |
rs549706380 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712285 | TTTCATTTAAAGTTT[A/G]CAGACACCCAGAGGG | 9870 |
rs549998616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671770 | AACAATCCTTGTTTT[A/C]GCAATGAAAACATTC | 9870 |
rs550009071 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690001 | GTCTGTAACCCCAAC[A/G]CTTTGGGAGGCTGAG | 9870 |
rs550060744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673733 | GCACACTGGGAGACC[A/C]AGCTTGGGCCAGAGT | 9870 |
rs550121656 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74701536 | ACTGCCTCCGTGATT[A/C]AATTATCTCCCACTG | 9870 |
rs550172988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709124 | TTAAACCCAAGTTAG[C/T]TAATAGCTAAAGTCA | 9870 |
rs550294465 | in-del | -/T | 0.288646 | 0.246995 | intron-variant | AREL1 | GRCh38.p7 | 14:74705043 | TACAGTCTTCTGTTG[-/T]TTTTTTTTTTTTTGA | 9870 |
rs550325029 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661798 | AAGATGCTCTGAAAA[A/G]GTGCTATGACTAGAG | 9870 |
rs550388590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670245 | CTGTGAGGATCAGAG[C/T]CCATCCAAATGTTAG | 9870 |
rs550414006 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707674 | TGGTGGGCGCCTGTA[A/G]TCCCAGCTACTTGGG | 9870 |
rs550438409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74678295 | TGAGTCCAGGAGTTC[A/G]AGACCACCCTGGGCA | 9870 |
rs550480424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708096 | TTTAGTAATAGTATT[G/T]TACCAATGTTAATTT | 9870 |
rs550541329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74666204 | AAAATTACTTTTTCC[C/T]CCATTTTAAAAGAAA | 9870 |
rs550674432 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680584 | GTTCACATAAAAACC[C/T]GTAAGTGAATATTTA | 9870 |
rs550695604 | snp | A/G | 0.0336253 | 0.125228 | intron-variant, utr-variant-5-prime | AREL1 | GRCh38.p7 | 14:74698800 | AGGCTGAGGTGGGAG[A/G]ATGGCTTGCGCCCAG | 9870 |
rs550729132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667146 | TACTAATTTTCACAT[G/T]CTAATTTTTTAAAGG | 9870 |
rs550746017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712536 | CACACCAAGGCTTCA[C/T]AATAAATGTGCATTG | 9870 |
rs550891116 | snp | A/C/T | 7.32187e-05 | 0.0060502 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713055 | GAGTTGGTCTCCACC[A/C/T]GGCCTGGGAACCGGC | 9870 |
rs550979717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688626 | CTCATGACCAGAGAG[C/T]TAGTTCTATCAATTC | 9870 |
rs550989475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74689277 | CTACTGCTACCCCTA[C/T]CCCACGCTATTCTCC | 9870 |
rs551046061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673934 | GTACACTGTGAGATC[C/T]TGCAGAAACACTAAA | 9870 |
rs551107527 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74682090 | TCCACTGGTGGCAAA[C/G]AGGTGGGTGATGATA | 9870 |
rs551255810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696891 | ATCACTTGAACTTGG[A/G]AGGCTTAAGTTGTAG | 9870 |
rs551371386 | snp | A/C | 0.000407058 | 0.0142605 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713037 | TCCCACCAACAGACC[A/C]CAGAGTTGGTCTCCA | 9870 |
rs551437291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677600 | CAACCTCTGCCTGTC[A/G]GGTTCAAGCGATTCT | 9870 |
rs551505254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74688700 | CAACAGCTCTCAAAC[C/T]ACTCCCCACCCCCAT | 9870 |
rs551539633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681530 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCTGAGGC | 9870 |
rs551644897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681999 | TCTTACAAATGCATA[C/T]GAATATACAATTATC | 9870 |
rs551652265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710289 | CACTAATTTAGCTCC[C/T]TATTAGGTATTAACA | 9870 |
rs551832825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688049 | TTTTTTTTTTTTGAC[A/G]GAGTCTCACACTGTC | 9870 |
rs551869344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680701 | GACCACAGAATATAC[G/T]TAGAGAATCCCTAAT | 9870 |
rs551921898 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74692587 | GGCTGAGAAGTGCCA[A/G]AGCTTCCTTCAGTTC | 9870 |
rs551925246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688434 | ACCTTGTGGAGTCCT[C/T]GGCCATTTTTCCCCT | 9870 |
rs552045143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703418 | ATCCCTCCCACAACA[A/G]TGGGAATTATGGGAG | 9870 |
rs552049941 | snp | A/C/T | 1.65611e-05 | 0.00287755 | intron-variant | AREL1 | GRCh38.p7 | 14:74663856 | AGTGATTAACTCATA[A/C/T]CACCAAAAACACTGG | 9870 |
rs552238012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684854 | AAAGGAACTTCTACA[A/C]CAGGGGTCAGTAACT | 9870 |
rs552239064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74706117 | ATACAAAACTGACTC[C/T]GCTATGCCTGAGCCA | 9870 |
rs552254683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677276 | AAGGCCAGAGAATCC[C/T]TTAAGGATCCCTTAA | 9870 |
rs552298482 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713893 | GGGGTGGGGCGAGGG[C/G]AGTGTTTCTTGTTGA | 9870 |
rs552323569 | snp | G/T | 3.32447e-05 | 0.00407691 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685629 | ATCAGGTCCCGTCAA[G/T]GCCAACAGACAGCCG | 9870 |
rs552359061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668846 | GCACATGCATCGGAA[A/T]TATCTCTGGGCCATC | 9870 |
rs552408599 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74683852 | CCTTGGTCTTACCAG[A/C]CCTTTATATTATCAA | 9870 |
rs552441590 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668997 | ATGTTCCAGCTTCAG[C/T]GCCCACTTCCTCCCA | 9870 |
rs552443714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691809 | AGATTTTTAATTACA[A/G]TAGCAACTAAATTTT | 9870 |
rs552457058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699750 | TTTGAAGGAGAAGTT[C/T]CCAAGAACCTATCAA | 9870 |
rs552466815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74683079 | AAGTGACTACTAACA[C/T]GTATGGGGTTTCTTT | 9870 |
rs552524427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668301 | TTAAAACCATCATCC[A/G]GGAATATTTGTGTAG | 9870 |
rs552603712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667926 | ATCCAAAATGAAACC[A/G]CTATTGACCTCTTCT | 9870 |
rs552963472 | snp | G/T | 1.65666e-05 | 0.00287802 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683493 | ACTCTTAGTCCCACA[G/T]GCCGATGTGCAGGGA | 9870 |
rs553028113 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AREL1 | GRCh38.p7 | 14:74689990 | TGGTGGCTCATGTCT[A/G]TAACCCCAACACTTT | 9870 |
rs553173293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697404 | TCAATTTTCAAAAAG[C/T]GCACAGGTTAGGGTG | 9870 |
rs553260697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680983 | AGGCCAGGAGTTAGA[A/C]ACCAGCTTGGTTAAC | 9870 |
rs553298004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74690512 | ATTCAGTTCAACAAG[C/T]AGGTATCAAATGCCC | 9870 |
rs553310495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698176 | TATCCTTTACCACTA[G/T]AGGTACTTGAGCCAA | 9870 |
rs553478180 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712685 | ACACGGTATATACTC[C/G]AGAACAATCATCCAC | 9870 |
rs553501164 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709270 | AGCAAGATCTAATAA[A/G]TAATAAATAAAAGGT | 9870 |
rs553636100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708650 | GTACAATATATAGAA[A/G]ATCAATTAACAGATG | 9870 |
rs553720645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691393 | CTTAACCTCTACAGT[G/T]AATCATGAAAAAGAA | 9870 |
rs553738666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670509 | TTAATTATTATAATA[A/G]TTAGTAGAGTAGACA | 9870 |
rs553782787 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662444 | GAAGTCAATGAGATT[C/T]TGAATCTTGAAATTA | 9870 |
rs553845131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685016 | AATGAGCCTTCGGAA[A/C]CAAAAATATTTACTC | 9870 |
rs554068566 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701090 | GGGTGCAAGTTGGGA[A/G]CCAACCCTGGATGGG | 9870 |
rs554123901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669590 | AAGTTCTCTTAGACA[C/G]TCCTGCTCTACAGGA | 9870 |
rs554168539 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74670446 | CTTTGTCTAGACAAA[A/G/T]ATCTAGTACAGGAAT | 9870 |
rs554223818 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665896 | ACCAGGAACTAAGAG[C/T]AGGATGTGGAACAAC | 9870 |
rs554434810 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692042 | GTCTGTTACCTTACC[C/T]TTAAACGAGGGCCCA | 9870 |
rs554493297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74706557 | AGCTGGATTTGAAGG[A/G]GAAACTCAACACTTA | 9870 |
rs554496696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698424 | AATGGGGTTACAGTC[A/T]AATTCACTCGATAAT | 9870 |
rs554562136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74705197 | GGCATGCGTCACCAC[A/G]CCCAGCTAATTTTGT | 9870 |
rs554627519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691193 | GATGTCATAGTGCAC[A/G]CCTGCAGTCCCAGTT | 9870 |
rs554673196 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661429 | GGTCTCCTTCAAAGA[C/T]GCTAAAAGGCCAGAA | 9870 |
rs554762632 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694141 | GATCATGCCACTGCA[C/T]TCCACCCTGGGCAAC | 9870 |
rs554897378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702976 | GTCATTCAACAAGTC[C/T]CCAGGAAGTTTCAAA | 9870 |
rs554901223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666634 | CACTCAATATATACC[C/T]GAAAAAATAAATTCT | 9870 |
rs555017283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666487 | AAAAATATATACTAT[A/G]TACTGTTTTGGTCTA | 9870 |
rs555027065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74691365 | CCTACGTCTAACTCC[A/G]AAGCTCAATGCTCTT | 9870 |
rs555088640 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684160 | ACAAATGTATTTAAA[C/G]AAACAGAAGGTGGGC | 9870 |
rs555128676 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AREL1 | GRCh38.p7 | 14:74698979 | CAGGGAGCCCTGACT[A/G]CTCCACTACACTTCA | 9870 |
rs555149971 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74688130 | TCCCGGGTTCGCGCC[A/G]TTCTCCTGCCTCAGC | 9870 |
rs555175965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671914 | CTAGGTTCAGACAGC[A/G]AGCCATGCCACACGG | 9870 |
rs555225033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702516 | ACAGCAGGGGGGACC[C/T]GGGCCCTGCCTTCAA | 9870 |
rs555261868 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663345 | AGGAGTATCAGCAGA[A/G]GGAGTTTTGGAGCAC | 9870 |
rs555273099 | snp | A/G | 4.94222e-05 | 0.00497078 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713213 | ATGGTGAGAGAAGAC[A/G]GTCCAAGAAGGGACG | 9870 |
rs555421179 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74709779 | TATAACTTGAAAATG[G/T]ACAAAAAAGTGAATC | 9870 |
rs555443484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686642 | TTTCTAGGCTCAGAT[A/C]TGGGAGGGACCAAAA | 9870 |
rs555548178 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713196 | AGGAGTTTGGCGTGA[C/G]CATGGTGAGAGAAGA | 9870 |
rs555698869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74707591 | ACAAGGTCAGGAGAT[C/T]GAGACCTTCCTGGCT | 9870 |
rs555826932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74679760 | TTGAACATGGGAGGC[A/G]GAGGTCGCAGTGAGC | 9870 |
rs555951068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700894 | AGAGAAAAAGGATCA[C/T]ACATTTTAAATGAAG | 9870 |
rs555960572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709125 | TAAACCCAAGTTAGT[C/T]AATAGCTAAAGTCAT | 9870 |
rs555961683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694862 | GGCACGGTGGCGGGT[A/G]CCTGTAGTCCTAGCT | 9870 |
rs555965054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678807 | AACTTTTGGGAAAAA[A/G]AGAGAACATCTTCAG | 9870 |
rs556139197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693087 | TAATGGGGTTGCAGC[A/T]CAGGGTCTGGAGCAA | 9870 |
rs556164952 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663286 | ATGAGAAGGACTCAA[A/G]TACCAGTCTGGTCAA | 9870 |
rs556197135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671094 | CCTAGTATGGAAACA[C/G]CAGAGGTCGGAGATC | 9870 |
rs556229764 | snp | C/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661162 | ACTTCAGGAGGAATT[C/T]CTGGGGAAATGCAAA | 9870 |
rs556349721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670585 | TGCTTATTTTACAGA[A/T]GAAATAATAAAGGCA | 9870 |
rs556403053 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74677794 | GCGTAAGCCACGGTG[C/G]CCAGCTAACCCTGTC | 9870 |
rs556425685 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702205 | GACTCTGTGTGGGAG[C/T]TTCAACCCCACATTT | 9870 |
rs556533129 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713408 | AAGAAGGGAAGGCAA[C/T]AGACAAGAGAAAAGA | 9870 |
rs556585401 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670967 | CTCTCCACATTCCCT[C/G]TATTGTACTACTCTG | 9870 |
rs556635238 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74674343 | GATGGCTCACATCTA[G/T]AATCTCAGCACTTTG | 9870 |
rs556647703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74682567 | AAGTACAGATTCACG[C/T]TACAGCATGACTGAA | 9870 |
rs556662428 | in-del | -/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661700 | AAAACCACAATAGTG[-/C]CAAAGGGTTTTGTTT | 9870 |
rs556785064 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74706918 | CCATAGAGTTAACAA[C/T]GCTTTGGGGGTCAAG | 9870 |
rs556793104 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692185 | AAGGGTCTATCCATC[A/G]GACTTTGTCACAGTA | 9870 |
rs556953579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688908 | GTGGCATAATCTTGG[C/T]TCTCTGCAACCTCCA | 9870 |
rs557198223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74664154 | AAGGAACAAGATACA[C/T]TAAAGTGGGGCTGTG | 9870 |
rs557198862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697309 | AAAGACGTTTGTTTT[A/G]TAAGATGCAATCTCC | 9870 |
rs557206050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711772 | AGATAAAGAAACTGA[A/G]ATGCAGATAGATTAA | 9870 |
rs557331024 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74704443 | ACTTGGAGTAGGGAG[C/G]GGGGCTTCCAGGTGA | 9870 |
rs557350137 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693731 | CCCAGAATCCCTGCT[C/T]TTAATGACTACTCTA | 9870 |
rs557387087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74665396 | GGGATTACAGGCGAG[C/G]TATTTCTGATGAACA | 9870 |
rs557428846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74689658 | GCTGGAGTGCAATGG[C/T]GTGATCTCAGCTCAC | 9870 |
rs557514301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673293 | CACAGCTCTATCCTG[C/T]GTACCAACCAACAAC | 9870 |
rs557520513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710928 | GTTCCAGTGCAACTA[C/T]GTTAAAATAAAATTG | 9870 |
rs557572233 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703651 | TAGATTCATACATGT[G/T]GTTACACATTTCGGT | 9870 |
rs557573735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664108 | GGCTGGGATCACACA[C/T]AGTAAACAAGCTAGG | 9870 |
rs557608789 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679742 | CTGAGGCAGGAGAAT[C/T]GCTTGAACATGGGAG | 9870 |
rs557635703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688118 | GAAAGCTCTGCCTCC[A/C]GGGTTCGCGCCATTC | 9870 |
rs557697920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74680205 | AAAGAAAGAAAGAAA[A/G]GAAAAGAAAAGAGAA | 9870 |
rs557707654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696213 | CTACACAACTACCTT[A/T]TATAAACAAATACAT | 9870 |
rs557785177 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697121 | CACCACTGTACTCTA[A/G]CCTGGGTAACAGAGA | 9870 |
rs557986591 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671959 | AAAACGGGTTTCCAG[A/C/T]CACACCTACCAGAGC | 9870 |
rs558006264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709827 | CATTGAAATACAAGA[C/T]GTTCTTTAAGGAGTC | 9870 |
rs558020522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703745 | CATTCACCAGATGAA[A/G]GACATTTGGGTTACA | 9870 |
rs558186170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74672544 | GAGTTCGAGACCAGC[C/T]GGAGCAATATGGCAA | 9870 |
rs558320793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669460 | ACAGCAGCTGCTAGC[C/T]AAGTGTAGTTATGTA | 9870 |
rs558417756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74678937 | ACTTTGTCACCCAGG[C/T]TGGAGTGTAGTGGCA | 9870 |
rs558440523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699098 | AGTGGTTAAGAGCAT[A/G]AATCTTACTACTGAA | 9870 |
rs558483149 | snp | A/G | 6.58913e-05 | 0.00573945 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713167 | ATTGCGCCGTTGGTG[A/G]TTACGGAAGAACCAG | 9870 |
rs558496915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74694717 | TAAAGAGGCTGGGCA[C/T]GGTGGCTCACGCCTG | 9870 |
rs558549077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676405 | ACAAAGAGCTTTCCT[A/C]TCTATGATCTAATCT | 9870 |
rs558589238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691284 | ATGATTGTGCTACTG[A/C]ACTCCAGCCTGGTTG | 9870 |
rs558619382 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706281 | AGTCTAGGAAGCTAT[C/T]ATTCCATTAACTGCG | 9870 |
rs558699803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676984 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 9870 |
rs558715951 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714413 | ACTCCATTAATAATA[A/G]TTTCTTTCTAGTTAA | 9870 |
rs558760888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74690732 | TGTTTTCAAGTTCAT[C/T]TCTTTAGTGTCCTTG | 9870 |
rs558761373 | snp | A/G/T | 0.000400723 | 0.0141497 | intron-variant | AREL1 | GRCh38.p7 | 14:74664811 | CATGGCACAAATCCA[A/G/T]CTGAAAGAAGTTTGG | 9870 |
rs558791614 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708726 | GCCTTCGCTCTGAAA[A/C]ACATGATGCAAATTG | 9870 |
rs558833621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697505 | TTCCACTCTTAGTTT[A/T]TACTCCCCAACCCAA | 9870 |
rs558867625 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670959 | TTTTATACTCTCCAC[-/T]ATTCCCTCTATTGTA | 9870 |
rs558891917 | snp | A/G | 0.000636047 | 0.0178219 | intron-variant | AREL1 | GRCh38.p7 | 14:74683575 | GTTAGCAAGCAGAGG[A/G]AAAAAACATTTCCTG | 9870 |
rs558913405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673572 | AATGACTACTCCAAA[C/G]TGATCAGAAGAAAAC | 9870 |
rs558952559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666053 | GTTTATCAGAAACTT[C/T]AGGCTGAGCTGTGGA | 9870 |
rs558953050 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672420 | TATATCTTTACTTAA[A/G]CAGAGAAATTTAAGT | 9870 |
rs558999926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74665802 | AGCTATAAAGAATAA[C/T]ACATTCTAACCAGAG | 9870 |
rs559157003 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74666536 | CTCATCTTTTGGTTT[C/G]TTTCCTTCACTTCAT | 9870 |
rs559250398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681325 | ACTACTGATACACTC[A/G]GTAACCTGGATGAAT | 9870 |
rs559436402 | snp | C/T | 0.00205812 | 0.0320129 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713022 | ACGGGCTCCCCACTC[C/T]CCCACCAACAGACCC | 9870 |
rs559591141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673843 | TTTCTGTAGGCATGC[A/G]TCCTTCCAGAATTTA | 9870 |
rs559637466 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669907 | ATTTCAGGGTTAATG[A/G]CCAGGGGCCTTAGTA | 9870 |
rs559761141 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714479 | CCCTTTATAAGAAGC[A/G]TATGGGGTAATACTT | 9870 |
rs559856692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700340 | CCATCTAGTTTATAA[A/G]TGAAGGAGTCAAGCA | 9870 |
rs559864048 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672532 | ACTTGAGTCCAGGAG[C/T]TCGAGACCAGCCGGA | 9870 |
rs559868569 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AREL1 | GRCh38.p7 | 14:74688336 | GGCCCTGAGTACTTA[C/T]TCAATGTGCCAGGTA | 9870 |
rs559870394 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74696484 | GACCAAATACTGTAT[C/G]CGGGTTGCTAAAATT | 9870 |
rs559915524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707139 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG | 9870 |
rs559932333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695654 | TGGTGCTCCTCTGCT[A/G]AAGATACCTCCGTTA | 9870 |
rs560018210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672138 | TTTAATTCAACAAGC[A/G]CTCTATTCCAGGGAT | 9870 |
rs560084514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664214 | GTAGGAACAGTTTGA[A/C]AAGCACTTCAAGAAT | 9870 |
rs560272869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697783 | TAGTCAGCAGGATGA[A/G]CTCACTCTCCTCAGT | 9870 |
rs560274091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693126 | ACAAGTGAGATGAAC[A/G]CACAGCCAGAACCAG | 9870 |
rs560337400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692515 | TTTCCTTGAGGCCTC[C/T]CTCCAACTCCATAAG | 9870 |
rs560374617 | snp | A/G | 3.31219e-05 | 0.00406938 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676679 | TACTATTTGAAGGGT[A/G]TGCGGCTGCCCACAG | 9870 |
rs560388117 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703995 | ATATCCACCAACACT[C/T]GGTACTGTCTTAATG | 9870 |
rs560391293 | snp | A/G | 1.65748e-05 | 0.00287874 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684546 | CCAGGTAATTTCCCC[A/G]CACGTAGTCATAAAT | 9870 |
rs560396473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74690957 | TGGATTTTTTTTTTT[A/T]AAGCTGGGCTTAAGG | 9870 |
rs560419369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668826 | ACACCACAATGTAAA[C/T]AGAAGCACATGCATC | 9870 |
rs560496525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74690074 | GCAATATAGTGGGAC[C/T]TCACCTCTACTAAAA | 9870 |
rs560561234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668254 | CCCCAATAAACTCCT[A/G]AGGGAACTTTGAAGG | 9870 |
rs560744119 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714507 | CTTTTCCCCCAAAAG[A/T]TAAAGCATCTGAATC | 9870 |
rs560761130 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74704858 | AAAGATTTTCTCCTG[G/T]TTTTTTTCTAGAGGG | 9870 |
rs560826171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74706688 | GCAATATGTTGGACC[C/T]TAAAGATTCCAGAAT | 9870 |
rs561011793 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74699585 | CTTATACATACTGCT[A/C]TCATTTATTTTAATA | 9870 |
rs561094156 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687976 | CAATAAAGGGTTAAA[A/T]ACTCATCCTAAAATA | 9870 |
rs561137436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704222 | TTATACATTCTAAAT[A/G]TGAACCCCGAATATC | 9870 |
rs561173110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668108 | TTCTAATCTCAGCCC[A/T]GATGCTAGCTTGCTA | 9870 |
rs561217765 | in-del | -/T | 0.419135 | 0.184101 | intron-variant | AREL1 | GRCh38.p7 | 14:74666719 | TTTACTACTCATTGA[-/T]TTTTTTTTTTTTTTT | 9870 |
rs561267425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74690844 | TTATTGAGTCACTTA[C/T]CACAGGCCAAACACT | 9870 |
rs561276758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696911 | TTAAGTTGTAGTGAG[C/T]CAAGATTGCGCCACT | 9870 |
rs561350298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74674634 | AAAAAAATATGACTG[A/G]CAATGCAGTTTCACA | 9870 |
rs561502645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701316 | GACGTATCAGAGACT[A/G]GTTAATTTACAAAGA | 9870 |
rs561629968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74693952 | GAGGCCAAGGCAGGC[A/G]GATCACTTGAGCCCA | 9870 |
rs561633129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74679106 | GGTCTCACTATGTTG[C/T]CCAGGCCGGTCTTGA | 9870 |
rs561716711 | snp | A/C | 1.6628e-05 | 0.00288335 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670060 | AGAGACACTTGCCCA[A/C]GAGCCGTCCCGCAAA | 9870 |
rs561814512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74680251 | AATGGACAAAAGACA[C/G]GAAGAGACATTTCAC | 9870 |
rs561852324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74670672 | GACACAGGTTGTCAG[A/G]TTCCCAGATCAGTTT | 9870 |
rs562026639 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74677089 | CAGGCGTGAGCCACC[A/G]CGCCCGGCTGGAATC | 9870 |
rs562221012 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661706 | ACAATAGTGCCAAAG[A/G]GTTTTGTTTAACAAA | 9870 |
rs562256207 | snp | A/G | 0.00155573 | 0.0278468 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712908 | GGTCTTCTGGGCTCT[A/G]CCTAAGGCTGGAGAG | 9870 |
rs562284150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74700305 | CAGAAGCACAGAAAG[C/T]TAAAATGACTTGCCT | 9870 |
rs562287513 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703350 | GAGACTTATTCACTA[C/G]CATGAGAACAGTATG | 9870 |
rs562288491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685395 | CAACTTTAGACTCCA[C/T]AGTAAACAGTGTCTG | 9870 |
rs562290799 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677009 | TTTCACTGTGTTAGC[C/T]AGGATAGTCTCGATC | 9870 |
rs562294000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685011 | ATTGAAATGAGCCTT[C/T]GGAACCAAAAATATT | 9870 |
rs562336914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707256 | GCCTGTAATCCCAGC[A/T]ACTCGGGAGGCTGAG | 9870 |
rs562358841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701208 | AAGGCAAATTTTCTA[C/T]GGTTGGGAGCCTGGA | 9870 |
rs562468382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74707862 | CTTGGGAGGCTGAGG[C/T]GGGAGAATGGCGTGA | 9870 |
rs562505416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685326 | TTCTCCTCCTTGACC[A/G]TTCCCCTTTATGTTA | 9870 |
rs562508494 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694252 | AACCTGGGTCAACTG[A/G]CTACTGGAACCAGCT | 9870 |
rs562513225 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699996 | GTTATGAGGGTGGTT[C/T]GTGCCAGGCCACAAT | 9870 |
rs562517770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676833 | ATGGAGTCTCGCTCT[G/T]TCGCCCAGGCTGGAG | 9870 |
rs562554851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74678323 | GCAACATAGTGAGAC[C/G]CTATTCCTACAAAAA | 9870 |
rs562577664 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661592 | CACACTGGCTAGTAT[A/G]AAAGCAGGATTAGAA | 9870 |
rs562580521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686806 | TTAGAGTGATTATCT[A/G]AAGTCCTACTAGAAA | 9870 |
rs562612226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686317 | TCATCCTCAGTCATG[A/C]CTGTCAAGGTAGGAG | 9870 |
rs562643306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693767 | TCTCCACTATGGGAA[A/G]CCAAGGAAGAAAGCA | 9870 |
rs562654120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677077 | GTGCTGGGATTACAG[A/G]CGTGAGCCACCACGC | 9870 |
rs562722799 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671750 | TTTCTTTTCCTTTTG[-/T]TTTAAACAATCCTTG | 9870 |
rs562815954 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662107 | ATCCTGGGGTATAGA[A/C/G]ACCCTGATGCTGGAT | 9870 |
rs562840841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74669847 | ACTGCTTAGAACCAC[C/T]TATCCCTTCAACCTT | 9870 |
rs562893159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699433 | AGACAGCACACAAGC[A/G]AGAGAGCCCTGCAAT | 9870 |
rs562916992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681807 | GAAAGAAACAGGTTG[G/T]GGGGGATAGGTGTGG | 9870 |
rs563052222 | snp | A/C | 0.00140333 | 0.0264518 | intron-variant | AREL1 | GRCh38.p7 | 14:74675950 | TCTTCTCATCCTCTG[A/C]AGTATAATAAGGAAT | 9870 |
rs563112309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698679 | CAGAGGAAGGAGAAG[C/T]AACTGTATGTGCAAG | 9870 |
rs563138912 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707755 | GCCGAGATCGCGCCA[A/C]TGCACTCCAGCCTGG | 9870 |
rs563227082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681228 | GTTTGGAGAGAAAAA[A/C]ACCACAAAACCACAC | 9870 |
rs563246480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664694 | CAAAACTCCTGACTT[C/T]GTGATCCGCCTGCCT | 9870 |
rs563276942 | in-del | -/CACA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697176 | ACACACACACACACA[-/CACA]GCCATGAAAAACATG | 9870 |
rs563396277 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74665938 | ATGTCCTTCCTTTCT[A/C]CTTACTTCTACAAAT | 9870 |
rs563432900 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711213 | TCCAGCCTGGGTAAC[-/AA]GAGCGAAACTAACTC | 9870 |
rs563451550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695615 | TCTTCCCACACCAGA[C/T]AGAATCAGCCACTTC | 9870 |
rs563735122 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687784 | TATTATCAATAGTAG[C/T]GCCAGTATCACTACT | 9870 |
rs563803651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702672 | TTCTGTAGCCAGTTT[C/G]AATTTCTCCTCAAAA | 9870 |
rs563899425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694188 | TCAAAATAAATAAAT[A/G]AATAAATAAATAAAT | 9870 |
rs564026699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687702 | TTAAATGAGTTAACA[C/G]ATGTAAGCAGCCTAC | 9870 |
rs564090113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74686948 | CCTTCCCAAACAAGT[A/G]TCTCATCTCTTGGGA | 9870 |
rs564101423 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666864 | AGCTGGGATTACAAG[C/T]GTGCATCACCACACC | 9870 |
rs564160460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74663862 | TAACTCATACCACCA[A/G]AAACACTGGGCATGC | 9870 |
rs564169714 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688271 | ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 9870 |
rs564199021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672775 | GTAACCTGCAGAATA[C/T]AGACATTCAATTGGA | 9870 |
rs564258359 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662892 | AGCCGGCCATACTTC[A/C]GTGCCAATAACAAAC | 9870 |
rs564454697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74695006 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 9870 |
rs564605689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709080 | AGAACCCTTCAAAGA[A/T]AAAGAAACCAAAGAA | 9870 |
rs564642758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74686237 | AATCAGACAAACTAA[C/T]GGGCCCTCTGGAAGA | 9870 |
rs564655421 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707442 | CCAAGGTGGGCGGAT[C/T]ACGAGGTCAGGAGAT | 9870 |
rs564756614 | snp | C/T | 0.000315261 | 0.0125511 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676156 | CACTTAGGACAATAA[C/T]GTCAAATTCACCATT | 9870 |
rs564773384 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694924 | AACCCGGGAGGCGGA[A/G]TTTGCCGTGAGCCAA | 9870 |
rs564866968 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713413 | GGGAAGGCAATAGAC[A/G]AGAGAAAAGAAGAGA | 9870 |
rs564998275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705835 | GTATACACAAAGGCA[C/T]AGCTTAGATTCAGCT | 9870 |
rs565021288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74675574 | AGTTGAAAGTGGCTT[C/T]CTATACAACTAGTTA | 9870 |
rs565035250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682851 | TCGCCTTCCACCATG[A/C]GTGGAAGCTTCGCGA | 9870 |
rs565083834 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662104 | AGGATCCTGGGGTAT[A/G]GAGACCCTGATGCTG | 9870 |
rs565092422 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702570 | CCAGGTCTGTGATGG[C/G]AGTGGCTGCTATGAA | 9870 |
rs565149407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695749 | ACTCCCCAAGGAACA[C/G]TGACCAGGTCATAAC | 9870 |
rs565186008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74674597 | ACAAAGTGAGACCCT[C/G]TCTCAAAAAATAAAA | 9870 |
rs565295317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703941 | GCGGCTGGACCACTT[C/T]GCATTTCCACCAGCA | 9870 |
rs565365253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682050 | TTTTTAAAAAGGCTG[C/G]TACATGTAAGGGTAT | 9870 |
rs565475381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712015 | CCAGCTTGATCAGTA[A/G]CTGGAGAATGGAAGA | 9870 |
rs565475499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74696163 | TTTATTGAAAAAGTA[C/T]ACCAATTCCAGGTGT | 9870 |
rs565500521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74664589 | GTAGCTGGGACTACA[G/T]GCATGTGCCACCACA | 9870 |
rs565506124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672496 | AATCCCAACACTTTG[A/G]GAGGCTGAGGCGGGT | 9870 |
rs565529294 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682639 | TGTGATTCCCAGTGT[C/T]GGAGGTGGGGCCTGG | 9870 |
rs565668534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703695 | TTCCTGCAGAGTAGT[A/C]CTCCATTAAATGGAC | 9870 |
rs565675689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74704293 | AGGTTGAAGACATAC[A/G]CCCAGGACACGGCCT | 9870 |
rs566038052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695264 | TTTGTATTTTTGGTA[A/G]AGGCAGGGTTTCACC | 9870 |
rs566070742 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708116 | AATGTTAATTTCTTA[C/G]ATGTGACAGTATGTG | 9870 |
rs566081544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679779 | GTCGCAGTGAGCTGA[C/G]ATTGTGCCATTGCAC | 9870 |
rs566103447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694614 | AAAAGTTTCTATTTC[G/T]GGAGAACACATTTTT | 9870 |
rs566142545 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677420 | AGGATCACTTTTGCC[C/T]AGGAGGTAAAGGCTA | 9870 |
rs566143879 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AREL1 | GRCh38.p7 | 14:74680492 | CACTCTGGAAAAGAA[C/T]TTGGCAATTTAAAAG | 9870 |
rs566276730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701573 | TCCCATAACACATGA[A/G]AATTATGGGAACTAT | 9870 |
rs566305680 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663136 | ACAAAAAAATATTCT[C/T]TTTAGCAGTCCTTAG | 9870 |
rs566412020 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74702267 | ATGAGGGCCCCACCC[C/T]ATAGCAGACTTCTGC | 9870 |
rs566421379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676937 | GAGTAGCTGGGACTA[C/T]AGGTGCCCGCCACCA | 9870 |
rs566426143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684122 | AGTCAATACATGATG[A/C]ATGGGTGTGGCTGTG | 9870 |
rs566498263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691259 | TAGGAGGTCAAGGCT[A/G]CAGTGAGCCATGATT | 9870 |
rs566618913 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74684802 | ACTGTAAGACTGCCA[A/C]AGAAACACTGCACTG | 9870 |
rs566662019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705122 | TCGGCTCACCGCAAC[C/G]TCCACCTTCCAGGTT | 9870 |
rs566685055 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AREL1 | GRCh38.p7 | 14:74689620 | TTTTTTTTTTGGGAC[A/G]GAGTTTCACTCTTGT | 9870 |
rs566712594 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697531 | CCCAAAATCCCACCA[C/T]AAAAGATTGCCCTCC | 9870 |
rs566724195 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705061 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 9870 |
rs566747510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688715 | CACTCCCCACCCCCA[C/T]AGTATTTACTGACCT | 9870 |
rs566836181 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AREL1 | GRCh38.p7 | 14:74666392 | CGGACTTCAGTTCTG[C/T]ATAGAATGGTATTTA | 9870 |
rs566917437 | in-del | -/TTTGC | | | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669376 | TGGAGATATGTGTCT[-/TTTGC]TTCACTCAAATGGGC | 9870 |
rs567192788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682288 | TACGGTTTCACTTCA[A/G]AAGTTACCCAGGGAC | 9870 |
rs567290024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698091 | GATATGTTGAATATA[G/T]TCATAGATATTCTGA | 9870 |
rs567292151 | snp | A/G | 6.62394e-05 | 0.00575459 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683405 | GGCCACTTTTACTAC[A/G]TTGGAATTGGGCTCC | 9870 |
rs567440824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667186 | CAATGAATGGAGGAG[C/T]GACAAAAGTGAAACC | 9870 |
rs567463240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704509 | CCCTTCCAAAGAAGG[A/C]AATCAGATATGCATC | 9870 |
rs567506007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74682198 | CCACTTTGTCCAGAG[C/G]CTTACTCTGCTATCA | 9870 |
rs567541017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703584 | ACATTTGTATCACAC[A/G]CAAAATGTAGTCCTT | 9870 |
rs567622638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673375 | ATTATTTTTCCCTTC[A/G]GTGATTTACATTTCA | 9870 |
rs567681830 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681637 | AATTAGCTGGGCGTG[A/C/G]TGGCACGTGCCTGTA | 9870 |
rs567733496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74666225 | TTAAAAGAAAACCTT[C/T]CTCCCTAAAGAAACG | 9870 |
rs567782014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695389 | CCAGCCTGAACTTTT[A/G]TTTCTATTCACTATG | 9870 |
rs567840531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695962 | TGCTGCTGGTCTCCT[A/G]GACCATGCTTTCAGA | 9870 |
rs567933538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74700652 | GGGCATGGTGGCACA[C/T]GCCTGTATTCCCAGC | 9870 |
rs567935386 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692049 | ACCTTACCTTTAAAC[A/G]AGGGCCCATGTTCTG | 9870 |
rs567986840 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681771 | GAGACGCCATCAAAA[A/C]AAAAAAGAAAAAAAA | 9870 |
rs568244577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677575 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 9870 |
rs568327443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686414 | TTTGATCATGTGAAC[A/C]AATAAAAGTACTGCC | 9870 |
rs568356845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706912 | ACTCTTCCATAGAGT[C/T]AACAATGCTTTGGGG | 9870 |
rs568397492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74669198 | ACTGCGCCCAGCCAA[A/G]AAGTTTAAAAATACC | 9870 |
rs568418134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668481 | GGATTTTTTTTTTAA[C/T]GTAAGCATTTCTATC | 9870 |
rs568539983 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74707889 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 9870 |
rs568604453 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704625 | TTAGTGATTTGGGGG[A/C]CCCAAGACTTATTTT | 9870 |
rs568647592 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673816 | AGTATTCTGAGTTGC[C/T]GCTAATTCCTGTTTC | 9870 |
rs568738268 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686854 | ACATTAGAATTGTCA[C/T]GTGGATGAAGGTGCT | 9870 |
rs568829937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74676985 | TTTGTATTTTTAGTG[A/G]AGACGGGGTTTCACT | 9870 |
rs568845170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670246 | TGTGAGGATCAGAGC[A/C]CATCCAAATGTTAGT | 9870 |
rs568849758 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690378 | GTCCAGAATGCCTAA[C/G]GATCAGGAATTTTCC | 9870 |
rs568978076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74706144 | GCCACAGAGGACAGG[C/T]CCCCATGTTCCCATC | 9870 |
rs569020220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74677300 | CCCTTAAGAAGTTCA[A/T]GACCAGCTTGAGCAA | 9870 |
rs569039807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699114 | AATCTTACTACTGAA[C/T]GATCTTAAACAAGTT | 9870 |
rs569069446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683138 | ACTGTGATGATGGCT[G/T]CATTTAAAGAACCAT | 9870 |
rs569132349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668417 | ACAGCAGGGATTCTC[A/G]ATGGATCTAAAAATG | 9870 |
rs569193414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74675954 | CTCATCCTCTGAAGT[A/G]TAATAAGGAATAAGG | 9870 |
rs569305820 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74710457 | TTTAAATGCAAATTA[C/G]TATTTAATGATATGC | 9870 |
rs569375393 | in-del | -/AATAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696980 | AAAATAAAATAAAAT[-/AATAA]AATAAAATAAAATAA | 9870 |
rs569421575 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696841 | TGGTGGCACACACCT[A/G]TAATCCCAGCTACTC | 9870 |
rs569444759 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74702924 | AGACCACCTCAGCCT[C/G]GATTTCAATGTCCAT | 9870 |
rs569470974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74679610 | GGTGGATGGATCACC[C/T]GAGGTCAGGAGTTTG | 9870 |
rs569521078 | snp | C/T | 1.65734e-05 | 0.00287862 | intron-variant | AREL1 | GRCh38.p7 | 14:74667409 | AAGTTAAAGTCATAC[C/T]CACACCATGGATACA | 9870 |
rs569535027 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AREL1 | GRCh38.p7 | 14:74678809 | CTTTTGGGAAAAAAA[A/G]AGAACATCTTCAGGA | 9870 |
rs569568173 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693997 | GCCTGGGCGACATAA[C/G]AAAACCCCGTCTCTA | 9870 |
rs569604261 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663958 | AATCTGAAATGAGGG[A/G]CAGAGGGCGGCAAAG | 9870 |
rs569685513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711179 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCATTG | 9870 |
rs569704025 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686497 | TTAGCACAGGCTGTA[A/T]ATGCTATTTTACAAT | 9870 |
rs569758370 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689146 | AGCCACCACGCCCAG[C/T]CAGGCCTCCCTATTT | 9870 |
rs569874187 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694111 | GCCCAGGAGGCAGAC[A/G]TTGACGTGAGCCGAG | 9870 |
rs569943467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74693549 | GGCAGGAACTGTTCT[C/T]AGTGCTTCATACACA | 9870 |
rs570039144 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677730 | CTGGTCTCAAACTCC[C/T]CACCTTGTAATTTGC | 9870 |
rs570069868 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74701545 | GTGATTCAATTATCT[A/C]CCACTGGATCCCTCC | 9870 |
rs570081425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686597 | TTTTATCAGCACTAG[A/C]ATATTACGTAGAGAC | 9870 |
rs570083063 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681297 | TGTACTACTCAGCAG[C/T]AAAAAGGAACCAACT | 9870 |
rs570119835 | in-del | -/TTTTTTTTTTTT | 0.334182 | 0.235401 | intron-variant | AREL1 | GRCh38.p7 | 14:74671322 | GGAGGTAAGAGTTGC[-/TTTTTTTTTTTT]TTTTTTTTTTTTGTG | 9870 |
rs570125037 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661811 | AAAGTGCTATGACTA[A/G]AGCTTAAAATGACAG | 9870 |
rs570162623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694320 | ATAAGAGAGCACTAT[A/G]TAGAATACTATATAA | 9870 |
rs570241303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74707518 | ATACAAAAAATGGCC[A/G]GGCACAGTGGCTCAC | 9870 |
rs570261828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686543 | TTCTTTTCAAGTCAG[C/T]GTACACTAAGGCTGT | 9870 |
rs570325653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693453 | GAAAGGGGGTTTATG[A/G]CAATGCATACACAAA | 9870 |
rs570330191 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74708144 | GTGCCATGGTTATGT[A/T]AGAAGTTAACATTAG | 9870 |
rs570637087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692863 | CGTGCACTACCACAC[A/C]TGGCTAATTTTTTAT | 9870 |
rs570642305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671033 | CTTTAGAAATCCCAC[C/T]CCTTTTTGTAGGATT | 9870 |
rs570699818 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74679302 | GTGGCACATGCCACA[C/G]TCCCAGCAACTTGGG | 9870 |
rs570705292 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664514 | GCTGCAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 9870 |
rs570706603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74678604 | CCACAAATATGTCCA[A/G]CTGCTTTTTGATAAA | 9870 |
rs570747520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74700742 | CTGAGATCATGCTAC[C/T]GCACTCCAGTCTGGG | 9870 |
rs570820392 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688784 | GTTCTACAAATTCCC[C/T]CTTTCTGGTTCCTCC | 9870 |
rs570829207 | in-del | -/G | 0.359787 | 0.224604 | intron-variant | AREL1 | GRCh38.p7 | 14:74681805 | AGAAAGAAACAGGTT[-/G]GGGGGGGATAGGTGT | 9870 |
rs570842151 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669205 | CCAGCCAAAAAGTTT[-/AA]AAATACCCAGGCATT | 9870 |
rs571037310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74689678 | TCTCAGCTCACCGCA[A/G]CCTCTACCTCTGGGT | 9870 |
rs571127129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670202 | GACCCTTCCTTCCCC[A/C]ACCCCATGCCAAAGG | 9870 |
rs571148595 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693180 | TGGTAAGGAATTGAG[A/C]CAATATTCAGCTGGA | 9870 |
rs571213785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74697288 | CACCAAATGACAAGA[C/G]AAAAGAAAGACGTTT | 9870 |
rs571268352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704386 | GGGAGACTTGAGACA[A/T]CAATCAAGATGTATA | 9870 |
rs571392871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74665171 | TATATTTATACAAGT[G/T]TTGGTGGCCCTACCT | 9870 |
rs571419437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703768 | GGGTTACATCCAGTT[C/T]GGTGGTATCATAGAT | 9870 |
rs571447274 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711579 | AAAATAAAATTGGCA[A/T]AAAATTCCAACCCTG | 9870 |
rs571462414 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74666102 | TTTCACATCTGAAGA[C/T]ATAAAACATGAAAAT | 9870 |
rs571508210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74710325 | GGAAATCAGAACACT[C/G]TCAATAGAGGTTACA | 9870 |
rs571620688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688537 | CTACATTTCTGCCCC[A/C]CCTCTATTCATCATT | 9870 |
rs571706450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695463 | AAATCAAATAACTCC[C/T]AGTTGTAATATAAGC | 9870 |
rs571786568 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AREL1 | GRCh38.p7 | 14:74666782 | TGGAATGCAGTGGTG[C/T]GATCTCGGATCACTG | 9870 |
rs571818671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681535 | ATCCCAGCACTTTGG[G/T]AGGCTGAGGCGAGCG | 9870 |
rs571825354 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74676466 | TGTCAGATGAAGATA[C/T]AGACAGCACAGAAGT | 9870 |
rs571865995 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690417 | TCTTCCTTGTAGATA[C/G]AGTTTGAAAGGATTT | 9870 |
rs571892095 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74686337 | AAGGTAGGAGTCTGA[-/G]GGGAAGACTTTCACT | 9870 |
rs571951628 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701930 | CAGTCAAATCTCAAA[A/G]CTCCAAAATGATCTC | 9870 |
rs572062860 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712869 | CCTTTTCCTCCCTCT[C/T]TCTCTGGAACTCTGG | 9870 |
rs572245471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74671250 | TTTTTCTTGACTCAT[A/G]GTTCCCTTTTCCTTG | 9870 |
rs572357654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678846 | ACCAAAGATTTCTTA[C/G]ACACCAACAGTTTGA | 9870 |
rs572580622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668613 | GACTCTAGCTGCCTT[A/C]CCATGCCAGCTCAGG | 9870 |
rs572624769 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672592 | AAATACAAAAATTAG[C/G]CAGGCATGGTGACAC | 9870 |
rs572640482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74667930 | AAAATGAAACCACTA[C/T]TGACCTCTTCTCTAA | 9870 |
rs572685855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74686193 | TAATAAGCAGTGGGT[C/T]TGAAAGTGAAGTCAT | 9870 |
rs572687940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700978 | CACAAGATAAGGGGC[C/T]ACTGGTCCAATGGAG | 9870 |
rs572775619 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683497 | TTAGTCCCACAGGCC[A/G]ATGTGCAGGGAAAGG | 9870 |
rs572811411 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74693666 | TAAAGTACTTTTCCA[A/C]GAAAACACACAGTGA | 9870 |
rs572820557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74674495 | TAATCCCAAGTACTC[A/G]GGAGGCTGAGGCACA | 9870 |
rs572953321 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694206 | TAAATAAATAAATAA[A/T]GCCAACAGACTTGCC | 9870 |
rs573015618 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691219 | CAGTTACTTGGGAGG[C/T]TGAGGCGGGAAGACT | 9870 |
rs573053608 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699400 | GAGAGAGAGAGCAAG[A/G]GCAAGAGAGAGAGAG | 9870 |
rs573133377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712810 | GGTGAGGAGAATGTG[C/T]TCCCCCAAACTACTG | 9870 |
rs573168728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703928 | ACCGTTTACCAAAGC[A/G]GCTGGACCACTTTGC | 9870 |
rs573191597 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702264 | TCCATGAGGGCCCCA[C/T]CCCATAGCAGACTTC | 9870 |
rs573221570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704619 | TTTAGCTTAGTGATT[C/T]GGGGGCCCCAAGACT | 9870 |
rs573228187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711827 | TAAGGCAGAGCAAGG[A/G]TTTTAACCCCATCAG | 9870 |
rs573308513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681664 | TGTAATCCCAGCTAC[A/T]CAGCGTGAGGCAGGA | 9870 |
rs573397845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681030 | TACAAAACAAAAAAT[C/G]AAAAAATTAACCGAG | 9870 |
rs573443582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74674419 | AGCCTGGCCAACATG[A/G]CAAAACTCAGTCTCT | 9870 |
rs573495955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673511 | AATAAATGGCAATAC[A/G]GTGATATATTAAATA | 9870 |
rs573598790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681816 | AGGTTGGGGGGGATA[A/G]GTGTGGCTGTAAAAG | 9870 |
rs573658294 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711268 | TTGGGGCTTGGCACA[-/T]GTGGCTCACGTCTGT | 9870 |
rs573810466 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693585 | TCACAGATACAATTA[C/T]CCCTATTTTAACACA | 9870 |
rs573890998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695644 | TCCTCCTTTGTGGTG[C/T]TCCTCTGCTGAAGAT | 9870 |
rs574018283 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74697346 | CTCCACAGAGAAGCA[C/G]CAGCCATGAGTCCAG | 9870 |
rs574114814 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665662 | CTCTACTTGATCAGA[C/T]ACATTTAAAAGTATG | 9870 |
rs574156078 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709229 | ATGGCTTGAGGCCAG[A/G]AGTTCAAGATCAGCC | 9870 |
rs574156356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74703339 | ACAGATATTGTGAGA[C/T]TTATTCACTACCATG | 9870 |
rs574196426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74687414 | GGCTTCAGAATCTCA[C/T]TGCTGTAAAAAGAGT | 9870 |
rs574262296 | in-del | -/T | 0.372592 | 0.217879 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713639 | GTTGTTATTATTTTG[-/T]TTTTTTGCTTATTAT | 9870 |
rs574428500 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74672130 | CATTTCCTTTTAATT[A/C]AACAAGCGCTCTATT | 9870 |
rs574446416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74707621 | TAACATGTGAAACCC[C/T]GTCTCTACTAAAAAT | 9870 |
rs574490802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699349 | AAGTGACAGTGAGGG[A/G]TGTGTGTGTGTGTGT | 9870 |
rs574502842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698505 | CATTTCACATTTCTT[C/G]AGCATTTGCTATATA | 9870 |
rs574534503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74684961 | TTTATAAATTGTCTA[C/T]GGCTACTTTTGCACT | 9870 |
rs574556796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700307 | GAAGCACAGAAAGCT[A/G]AAATGACTTGCCTAT | 9870 |
rs574567955 | snp | A/G | 0.000712599 | 0.0188624 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684492 | GGCCCACCTCATAGG[A/G]GTCCTTCCAATCCCA | 9870 |
rs574591728 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661880 | CTCTGGAAGGCTGCC[A/G]GAGGGGAGAATTCAG | 9870 |
rs574658343 | snp | C/T | 1.68826e-05 | 0.00290534 | missense | AREL1 | GRCh38.p7 | 14:74667570 | TGACTGGAGTTTGAG[C/T]TCCACCTGTCATGAG | 9870 |
rs574766756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705433 | ATGCTTAAGTTTAGC[C/T]AAGGTTTTAGTCCCT | 9870 |
rs574788121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706464 | TGAAAGGAAAAACAA[C/T]GTTAATTAAATGAGC | 9870 |
rs574871819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691376 | CTCCGAAGCTCAATG[A/C]TCTTAACCTCTACAG | 9870 |
rs574883781 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702210 | TGTGTGGGAGCTTCA[A/G]CCCCACATTTCCCCC | 9870 |
rs575025222 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712957 | GGGTTGCAGCGCGAC[A/G]AAGTTCCACCTCCGC | 9870 |
rs575068426 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74678391 | TAGTCCCAGCTACTC[A/C/G]GGAGGTTGAGGCAGG | 9870 |
rs575087825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74668649 | GGGTCTAATCCCATG[G/T]GTACAAAGGCAGACA | 9870 |
rs575276957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74704744 | CACTTTTTAAAGAGT[A/G]CAAGTTTCTAACTTT | 9870 |
rs575381795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74706665 | ATTAAGAAGCGACCA[C/T]ATGCCAAGCAATATG | 9870 |
rs575504218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74683608 | TAGAGTGAGTGGGGA[A/G]AGAGGAAGTAGCTGG | 9870 |
rs575571512 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698593 | AACCTCAATGAACTT[C/G]GTCCGCCATGGGAGA | 9870 |
rs575617162 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74698406 | CAAATCTGGGAGGCA[A/T]GAAATGGGGTTACAG | 9870 |
rs575629631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74702442 | CAAGCTGTACCTTGG[C/G]TCCTTTCAGCCACAG | 9870 |
rs575638107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74701820 | CTAGATACAATGGGA[A/G]TACAGGCAATGGGTA | 9870 |
rs575640010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709699 | GAAAAATAATTAACA[A/G]CGACTAATGTTTGTT | 9870 |
rs575662746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74689945 | TTTAGAGTGGTAATG[A/G]GTAGTCTTAAAAATC | 9870 |
rs575709114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74674302 | AAAAAGGCAAATTAA[A/G]AATATTACCCTGATG | 9870 |
rs575745847 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691066 | GCTCATACCTGTAAT[A/C]CCAGCACTTTGGAAG | 9870 |
rs575788821 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AREL1 | GRCh38.p7 | 14:74671136 | ACATTTCTCTCAAGG[C/T]AACCACGGTTCAAAC | 9870 |
rs575814890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74673577 | CTACTCCAAACTGAT[C/T]AGAAGAAAACTATTT | 9870 |
rs575900677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74708766 | TCAAGATAACAAAAA[C/T]TCATAAAATCATATG | 9870 |
rs575943575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693868 | AAATAAATAAGTATA[G/T]GTATTTAGTTTAAAA | 9870 |
rs575970354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74698999 | ACTACACTTCAGACC[A/G]TGTGAAGAGCAAGAC | 9870 |
rs576046849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74685330 | CCTCCTTGACCGTTC[C/T]CCTTTATGTTATGAA | 9870 |
rs576114301 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662109 | CCTGGGGTATAGAGA[C/T]CCTGATGCTGGATCC | 9870 |
rs576119051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74694914 | GAATGGTGTGAACCC[A/G]GGAGGCGGAGTTTGC | 9870 |
rs576139637 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661351 | ACGAATCTGCAGCAG[C/G]GCTTGGTCTCTGCCA | 9870 |
rs576177513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74670654 | CAGTAAAATTAAGAA[C/T]AGGACACAGGTTGTC | 9870 |
rs576332723 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662707 | CGTAAACTCCTAGTC[C/T]CTGTTCCTTTGTCTT | 9870 |
rs576378024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74686039 | GTAATGGAGTCACTT[C/T]CCCCTTATGTTTGCC | 9870 |
rs576386068 | in-del | -/CT | 0.0126979 | 0.078662 | intron-variant | AREL1 | GRCh38.p7 | 14:74682784 | CCCAGCACCTCCTCC[-/CT]CTCTCTCTCTCTTGC | 9870 |
rs576390022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74692980 | TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAGTC | 9870 |
rs576556261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74700216 | TAAAGTGCTACATCT[A/G]TATTATCTCATTTAA | 9870 |
rs576587449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74699512 | TGGCCACCCTCAACC[A/G]TGGACTGGAATAATT | 9870 |
rs576713604 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666377 | TGCCCACACCTGATA[C/T]GGACTTCAGTTCTGC | 9870 |
rs576784802 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AREL1 | GRCh38.p7 | 14:74707361 | TGACAAGAGCGAAAC[C/T]CCATTTTAAAAAAAA | 9870 |
rs576821600 | in-del | -/TTTA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702642 | GTGATTTGGCTCCTC[-/TTTA]TTTATGCAAATTTCT | 9870 |
rs576829265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74691417 | AAAAGAATAAAGTCA[C/T]AAGGATAGTGAAGTA | 9870 |
rs576836202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AREL1 | GRCh38.p7 | 14:74701708 | CAACAGTCCTCCAAA[A/G]TCTTAACTCAAAGTT | 9870 |
rs576956105 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666684 | TAGGATTTTATAGAC[A/G]GTACATGATATTAAC | 9870 |
rs576980585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693230 | GCTTTAAAGCCCAAT[C/G]TATCAGCCTATGCAG | 9870 |
rs577118603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74670552 | GTTTTTAGTCAAATA[A/T]TCAGCTGCCTGCATT | 9870 |
rs577152645 | in-del | -/A | 0.440195 | 0.162252 | intron-variant | AREL1 | GRCh38.p7 | 14:74678696 | AAGACATGTATAAGC[-/A]AAAAAAAAAAAAAAA | 9870 |
rs577162273 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694787 | GAGGTCAGGAGATCA[A/G]GACCATCCTGGCTAA | 9870 |
rs577170780 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678955 | GAGTGTAGTGGCAAG[A/C]TCACAGCTCACTGCA | 9870 |
rs577195551 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662015 | CTTCCGGTACATATC[C/T]CATGGGAAAACATTT | 9870 |
rs577215226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74681176 | AGGTGACAGAGCAAG[A/G]CCCTGTCTCAAAAAC | 9870 |
rs577223352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74688261 | CGATCTCATGACCTC[A/G]TGATCCACCCGCCTC | 9870 |
rs577405849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74705765 | GATTCTCTCTATTGC[A/G]CCATTCTCTCTAAAA | 9870 |
rs577527242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AREL1 | GRCh38.p7 | 14:74703916 | AGAAACTGCCAAACC[A/G]TTTACCAAAGCGGCT | 9870 |
rs577614465 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667781 | GCTTCAGGGTTCCTA[A/C]CACTATTGCTGTATA | 9870 |
rs577626190 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | AREL1 | GRCh38.p7 | 14:74689380 | ATACAGCTCTGAAAT[-/G]TCCCCTCTCCATTCC | 9870 |
rs577748695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74703255 | TCAGAAGGCAAAAGG[C/G]ATGTCTTACGTGGCA | 9870 |
rs577802759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74702652 | TCCTCTTTATTTATG[C/T]AAATTTCTGTAGCCA | 9870 |
rs577834621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74695560 | ACTCAACTCAAGCAC[C/T]CCCCCTTCTCTGGTC | 9870 |
rs577930011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74672084 | CACATCAGGTGTTCC[C/T]TTTCCATCAGACCAA | 9870 |
rs577977666 | snp | A/G | 6.99117e-05 | 0.00591194 | intron-variant | AREL1 | GRCh38.p7 | 14:74671373 | CGAGTGGGGAGGAGA[A/G]TTCAAAAAGATGAAT | 9870 |
rs578085826 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663563 | GCAGGTGAGGTAAAG[A/G]CAAGGCTTGTAGGTG | 9870 |
rs578110695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74709867 | CCAGAATAATTTTAC[A/C]AAGAAATTTGATACC | 9870 |
rs578125583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AREL1 | GRCh38.p7 | 14:74693763 | TGCCTCTCCACTATG[A/G]GAAACCAAGGAAGAA | 9870 |
rs578254445 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687599 | AAATCCATGCCCCAT[C/T]ATTCATAATGTGACC | 9870 |
rs578256740 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AREL1 | GRCh38.p7 | 14:74687329 | AACCCTTCTGTGAGA[A/G]ACAGCTGACATGCAG | 9870 |
rs745351391 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668820 | TGTTTAACACCACAA[A/T]GTAAATAGAAGCACA | 9870 |
rs745362382 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705515 | AAAACAACAACTAAA[C/T]TCCACAACCCAGAAC | 9870 |
rs745435768 | snp | A/G | 1.67396e-05 | 0.00289301 | intron-variant | AREL1 | GRCh38.p7 | 14:74676570 | ACACAGATAAAGAAG[A/G]GAGACTGCTTACCTC | 9870 |
rs745443416 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672205 | CACCTGCCCTACATG[C/G]GAGTTCCAAGGGACC | 9870 |
rs745482901 | snp | C/G | 1.66829e-05 | 0.00288811 | missense | AREL1 | GRCh38.p7 | 14:74667535 | CAGCAAATTTAAATA[C/G]AAGATTTTATTCGCA | 9870 |
rs745534401 | snp | C/G | 1.65968e-05 | 0.00288065 | intron-variant | AREL1 | GRCh38.p7 | 14:74667450 | CTTCAAGGCCAAGAA[C/G]AGACAGGATCCCACC | 9870 |
rs745558326 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704779 | AAAGCCAACATAAAT[A/T]TTTTCTTCATAGTTT | 9870 |
rs745608357 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692096 | CTCCTATTCACCAAA[C/G]CAGGTAACTTTTGGC | 9870 |
rs745630286 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684093 | CATAACTACTCAGGT[A/G]TGAAAACAGCCATAG | 9870 |
rs745645128 | snp | C/T | 1.6609e-05 | 0.0028817 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670018 | CTCGGACCAACTGCT[C/T]GTAGGCTCCTCCTAG | 9870 |
rs745720205 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685485 | AGGTACATTCTGGCA[C/T]GACTAGAAATATTTT | 9870 |
rs745754956 | in-del | -/A | 1.67728e-05 | 0.00289588 | intron-variant | AREL1 | GRCh38.p7 | 14:74676567 | AGCACACAGATAAAG[-/A]AGGGAGACTGCTTAC | 9870 |
rs745767146 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697651 | TTCTTCATCAGTCAG[A/C]CTCTCCAGTCTCTTA | 9870 |
rs745778685 | snp | C/T | 1.65603e-05 | 0.00287747 | intron-variant | AREL1 | GRCh38.p7 | 14:74663873 | ACCAAAAACACTGGG[C/T]ATGCATCAGGCGGGC | 9870 |
rs745806741 | snp | A/G | 1.65594e-05 | 0.0028774 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663786 | CCTGTGCACCTCTTC[A/G]TAGGAGTCATATGTA | 9870 |
rs745831533 | snp | C/G | 5.07138e-05 | 0.00503531 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670091 | CTCATACATTTTCAG[C/G]CGCAGATGAGCGGGG | 9870 |
rs745834411 | snp | C/T | 1.66413e-05 | 0.0028845 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685652 | GACAGCCGAGGATCA[C/T]AGCTGCAGCTGTTAA | 9870 |
rs745859906 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697590 | TATACAGTTGTCTAT[A/T]TCTGCTATTGTGGTT | 9870 |
rs745888137 | in-del | -/ATA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710495 | CCTCTGAACCTATAT[-/ATA]ATACTAATGAGTCAA | 9870 |
rs745902318 | in-del | -/AAAAT | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711543 | GGAGGCTCTGTCTCA[-/AAAAT]AAAATAAAATAAAAT | 9870 |
rs745909947 | snp | A/T | 1.66891e-05 | 0.00288864 | intron-variant | AREL1 | GRCh38.p7 | 14:74667299 | AGTTAAGAATGGGAG[A/T]CTGAATTGCAATCAC | 9870 |
rs745919811 | snp | A/T | | | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675911 | TGCTCACGCCTGAAG[A/T]GGACACATTGCGTTC | 9870 |
rs745937103 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683367 | ACTGTGATTTCATAA[C/T]GCCCAGCCTTGCGCA | 9870 |
rs745949543 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710586 | TGTCTAATCACCAAG[A/T]GATACATCAAAAAAC | 9870 |
rs745951568 | snp | A/C/G | 6.58917e-05 | 0.00573952 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713156 | GACGTAGAAGTATTG[A/C/G]GCCGTTGGTGATTAC | 9870 |
rs745952028 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679266 | CATCTCTACAAAAAA[C/T]ATAAAAATTAGCCAG | 9870 |
rs745964406 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696838 | GCATGGTGGCACACA[C/T]CTGTAATCCCAGCTA | 9870 |
rs745977888 | snp | A/G | 3.3394e-05 | 0.00408606 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713096 | GCCCTTTCCCCAAGG[A/G]GTTTCCGCTTCCGGG | 9870 |
rs746043990 | snp | C/T | 1.68875e-05 | 0.00290576 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674089 | GGGATGATCTTCAGG[C/T]AGAACTCCTTCACTG | 9870 |
rs746198639 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690963 | TTTTTTTTTTAAGCT[A/G]GGCTTAAGGTTGCTG | 9870 |
rs746224272 | snp | C/T | 0.000163172 | 0.00903102 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661337 | TTTCACCTGGCCTGA[C/T]GAATCTGCAGCAGGG | 9870 |
rs746231145 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688278 | GATCCACCCGCCTCA[C/G]CCTCCCAAAGTGCTG | 9870 |
rs746267641 | snp | C/G/T | 9.96672e-05 | 0.00705871 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684618 | AGCTGACTACACGTG[C/G/T]GGCAAGCTCAAAGAG | 9870 |
rs746270046 | snp | C/T | 1.72412e-05 | 0.00293604 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675922 | GAAGTGGACACATTG[C/T]GTTCGACGATATTCT | 9870 |
rs746311058 | snp | G/T | 1.67172e-05 | 0.00289108 | intron-variant | AREL1 | GRCh38.p7 | 14:74671404 | ATAAAATTTCAAAAC[G/T]GACCTTCTTCATCCT | 9870 |
rs746322111 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668519 | CTGAGAAATAAATTA[C/T]TAAGATTTAGTATTC | 9870 |
rs746327805 | snp | A/T | 3.31307e-05 | 0.00406992 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664890 | ATGGGCTTTGAAGTC[A/T]GACACACTGATGTCT | 9870 |
rs746380778 | snp | C/G | 1.68471e-05 | 0.00290228 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670869 | GCCCTCCCCAGTCCA[C/G]AGCTGAAAAGCATAA | 9870 |
rs746386337 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669213 | AAAGTTTAAAAATAC[C/G]CAGGCATTGTGTTAA | 9870 |
rs746414858 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708199 | GAATACTCTGTACTA[C/T]CTTTGCAACTTTTTT | 9870 |
rs746430534 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701054 | TCATTAGTCACATTG[G/T]TTGAGGGTGGCCAGG | 9870 |
rs746495433 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694805 | CCATCCTGGCTAACA[C/T]GGTGAAATCCCGTCT | 9870 |
rs746549442 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713970 | TGGTACTCAAATATT[C/T]TTGTCAGAGAAAATG | 9870 |
rs746549816 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665249 | GGAAGAAAAAAAATT[A/G]CTCAGGTATTTCTTT | 9870 |
rs746569722 | snp | A/C/G/T | 0.000150056 | 0.00866075 | intron-variant | AREL1 | GRCh38.p7 | 14:74685558 | AAGGACCCAAGCAAC[A/C/G/T]TTTACAAAAATATAA | 9870 |
rs746583942 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678448 | GGCTGCAGTGAATCA[G/T]GATCGCACCACTGCA | 9870 |
rs746619206 | snp | A/G | 4.97014e-05 | 0.0049848 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672832 | GAAATTTTACCTACC[A/G]ATTCCAACAAGGCAT | 9870 |
rs746621938 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693577 | ACATAAACTCACAGA[C/T]ACAATTATCCCTATT | 9870 |
rs746622055 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707116 | CTCATGCCTATAATC[C/T]CAGCACTTTGGGAGG | 9870 |
rs746672169 | snp | A/G | 3.32984e-05 | 0.00408021 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671468 | AGATGGAGAAATTCC[A/G]AGTGGCTTTCAGAGA | 9870 |
rs746779251 | snp | A/T | 1.70272e-05 | 0.00291776 | intron-variant | AREL1 | GRCh38.p7 | 14:74673269 | CCCTCAAGGCCAGTA[A/T]AAGTCCTCCACAGCT | 9870 |
rs746786671 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672306 | CCAAATTTAGTAGAA[C/T]CAAATAGAAGAACAG | 9870 |
rs746816241 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705817 | CGTATTTCTTTTTGT[A/G]TAGTATACACAAAGG | 9870 |
rs746856228 | snp | C/T | 1.65647e-05 | 0.00287786 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683334 | GGACTATATGCCACA[C/T]TTAATCCACCAAGCT | 9870 |
rs746872766 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673510 | CAATAAATGGCAATA[C/T]GGTGATATATTAAAT | 9870 |
rs746900273 | snp | A/G | 1.65638e-05 | 0.00287778 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663687 | CCAGAAGCTCCAGAG[A/G]GCATGGGAGCCAACT | 9870 |
rs746901497 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693333 | TAAAATCTGCTACTA[C/T]GAGTCAGGGGAAAAT | 9870 |
rs746926987 | snp | C/G | 1.66131e-05 | 0.00288206 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670010 | GAAGCGAGCTCGGAC[C/G]AACTGCTTGTAGGCT | 9870 |
rs747015131 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692083 | ACCAAGTAGAGCACT[-/C]CTATTCACCAAAGCA | 9870 |
rs747037785 | in-del | -/TA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690702 | ATTTCATCAAATTGT[-/TA]TGAGTACTTTGTGTG | 9870 |
rs747055254 | snp | C/T | 1.66355e-05 | 0.002884 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670855 | CCATTCCCGGCGAGG[C/T]CCTCCCCAGTCCAGA | 9870 |
rs747062960 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707082 | TCAAAATTATACACG[A/G]TCTGGTCGGGCACAG | 9870 |
rs747063113 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699465 | GAATGGCGTCCCATC[A/C]AGCGCTGGTTCCCAA | 9870 |
rs747069956 | snp | G/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712197 | ATATGTAAAATAAAA[G/T]AATTTATGTTATTGA | 9870 |
rs747099452 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697777 | CCTCATTAGTCAGCA[A/G]GATGAACTCACTCTC | 9870 |
rs747136919 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663174 | CCAGTGCCATGGCCT[A/G]TGCCTACCATTGTGC | 9870 |
rs747264458 | snp | A/T | 8.39144e-05 | 0.0064769 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713093 | ATTGCCCTTTCCCCA[A/T]GGAGTTTCCGCTTCC | 9870 |
rs747264626 | snp | A/C/G | 0.000317139 | 0.0125886 | intron-variant | AREL1 | GRCh38.p7 | 14:74683256 | GGAAAGAGAGAGAGG[A/C/G]AAGGAGACAAAGGGA | 9870 |
rs747268645 | in-del | -/GTGTGTGTGTGTGAGAGA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699365 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGAGAGA]GAGAGAGAGAGAGCA | 9870 |
rs747281516 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664315 | TACTCCTGTGGCAGT[C/T]AGCATGACAGCCCTT | 9870 |
rs747297738 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710632 | CTACACATGAATGGC[A/G]GCTTGACAGAGACAA | 9870 |
rs747315835 | snp | G/T | 1.65663e-05 | 0.002878 | missense | AREL1 | GRCh38.p7 | 14:74664876 | CCAACAACTACTGCA[G/T]GGGCTTTGAAGTCAG | 9870 |
rs747317541 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664613 | ACCACACCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 9870 |
rs747344337 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690606 | ACTTTTTGCTATTCA[C/T]AATTTTCCTGTATGA | 9870 |
rs747373824 | snp | A/C | 1.66963e-05 | 0.00288927 | intron-variant | AREL1 | GRCh38.p7 | 14:74684424 | TACTCAGAAACCCCA[A/C]TGGGTATGGAGACAG | 9870 |
rs747387615 | snp | A/G | 4.97236e-05 | 0.00498591 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684525 | AGACTTTGCAAGACC[A/G]GGGATCCAGGTAATT | 9870 |
rs747390404 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74676027 | GCTTTTAGTCCACAG[A/G]ACAAGCCAAATGTGG | 9870 |
rs747438330 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691646 | CACTTGCTTACGAAG[A/G]TTCCTGGTCTGGTTG | 9870 |
rs747447156 | snp | C/T | 1.66668e-05 | 0.00288672 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713531 | CCATGAAGCGAATGC[C/T]TAGTCTCAGAGATCA | 9870 |
rs747523844 | snp | A/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663168 | GGCAGTCCAGTGCCA[A/T]GGCCTATGCCTACCA | 9870 |
rs747642166 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682616 | ACCCTCCAAATCGCA[C/T]GTTGAAATGTGATTC | 9870 |
rs747669740 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702419 | TTGCACCTTCTGAAG[C/T]GATGGCCCAAGCTGT | 9870 |
rs747731381 | snp | A/G | 0.000151318 | 0.00869689 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669612 | TCTACAGGAAACTGG[A/G]GAACATAGGACCCAG | 9870 |
rs747758193 | in-del | -/G | 0.000119763 | 0.00773738 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713073 | CCTGGGAACCGGCTC[-/G]GGGGATTGCCCTTTC | 9870 |
rs747808877 | snp | C/T | 6.62658e-05 | 0.00575574 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663669 | GATGTCTGTAACTTG[C/T]GCCCAGAAGCTCCAG | 9870 |
rs747824738 | snp | A/T | 1.67694e-05 | 0.00289558 | intron-variant | AREL1 | GRCh38.p7 | 14:74676126 | GCACTAAATCATACT[A/T]TTCTTTTAACTTACC | 9870 |
rs747828437 | snp | A/G | 1.82657e-05 | 0.003022 | intron-variant | AREL1 | GRCh38.p7 | 14:74684716 | ACAAACCGCCTGCCA[A/G]TTACACATTACAGCT | 9870 |
rs747851228 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694456 | CCAAATTTAGAAACA[C/T]AACATTACATAAAGA | 9870 |
rs747876203 | snp | C/T | 4.97343e-05 | 0.00498645 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664842 | TCCATTTACCTTTTC[C/T]CTGAAATGCCATGAG | 9870 |
rs747880282 | snp | C/G | 0.000133502 | 0.00816905 | intron-variant | AREL1 | GRCh38.p7 | 14:74678368 | CTAAGCACGGTGGTG[C/G]ACGCCTGTAGTCCCA | 9870 |
rs747891710 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661789 | ATGGTGCCTAAGATG[C/T]TCTGAAAAAGTGCTA | 9870 |
rs747933658 | snp | A/C | 1.64827e-05 | 0.00287073 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713051 | CCCAGAGTTGGTCTC[A/C]ACCCGGCCTGGGAAC | 9870 |
rs747961555 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707260 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCCG | 9870 |
rs747972822 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673681 | AACAATGTATTTTAA[A/T]ATATGAGAGTGGTGC | 9870 |
rs747978586 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662005 | GGTGATAAACCTTCC[A/G]GTACATATCCCATGG | 9870 |
rs748014813 | snp | C/G | 1.65712e-05 | 0.00287843 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676730 | GTGGCACACAATTTT[C/G]GTCTTAGAAGGAACC | 9870 |
rs748044925 | snp | C/T | 0.000165725 | 0.00910137 | synonymous-codon, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669676 | ACCTGATTTATTATA[C/T]TTCTCTTCTGCAAAG | 9870 |
rs748098405 | snp | C/G | 3.32088e-05 | 0.00407471 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673126 | TGCTAGAATGTTCCT[C/G]TCCTTACAGCTGAGC | 9870 |
rs748140271 | snp | A/G | | | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669586 | CAGAAAGTTCTCTTA[A/G]ACAGTCCTGCTCTAC | 9870 |
rs748164728 | in-del | -/A | 0.000207139 | 0.0101748 | intron-variant | AREL1 | GRCh38.p7 | 14:74675665 | CACACAGGTTCAAGC[-/A]GGGGGATTTTATGTC | 9870 |
rs748168958 | snp | C/T | 1.7151e-05 | 0.00292835 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670107 | CGCAGATGAGCGGGG[C/T]GATTAGGGTTGGGAT | 9870 |
rs748214335 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700754 | TACTGCACTCCAGTC[C/T]GGGCGACAGAGCGAG | 9870 |
rs748223905 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675765 | GGTGTGGCACTCAGA[A/G]GGCGAGTCTTCATCT | 9870 |
rs748231133 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685921 | TTGCTTTATTGCTAA[C/T]TTCAAAATGCAGTAA | 9870 |
rs748248260 | in-del | -/AAG | 0.00010102 | 0.00710633 | intron-variant | AREL1 | GRCh38.p7 | 14:74671489 | CTTTCAGAGACTGAA[-/AAG]AAGTGAAAGGAAGGG | 9870 |
rs748289816 | snp | C/G/T | 0.000132586 | 0.00814117 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684523 | GGAGACTTTGCAAGA[C/G/T]CGGGGATCCAGGTAA | 9870 |
rs748302597 | in-del | -/A | 1.65787e-05 | 0.00287907 | intron-variant | AREL1 | GRCh38.p7 | 14:74664116 | TCACACACAGTAAAC[-/A]AGCTAGGATTAGATC | 9870 |
rs748321330 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672527 | GTATCACTTGAGTCC[A/G]GGAGTTCGAGACCAG | 9870 |
rs748325871 | snp | A/G | 3.4965e-05 | 0.00418106 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664042 | CTCCTCCTGGGTCAG[A/G]CTGGAAACCACAGTC | 9870 |
rs748337163 | snp | C/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713417 | AGGCAATAGACAAGA[C/G]AAAAGAAGAGACTTT | 9870 |
rs748337269 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699680 | CATAGGAACTTAATT[C/T]TTGTTTATATCAATT | 9870 |
rs748419474 | snp | C/T | 1.70145e-05 | 0.00291667 | intron-variant | AREL1 | GRCh38.p7 | 14:74670744 | TCCACATTTTCCACC[C/T]ACCCGTCACCAACTC | 9870 |
rs748423429 | snp | G/T | 4.22583e-05 | 0.00459645 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712962 | GCAGCGCGACGAAGT[G/T]CCACCTCCGCTGTCC | 9870 |
rs748463029 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682551 | CAATAAAAAGAAATG[-/A]AAGTACAGATTCACG | 9870 |
rs748465722 | snp | A/G/T | 4.94241e-05 | 0.00497092 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713247 | TCAGGCCACTTTTTG[A/G/T]GTGGAGAAGGAGGTA | 9870 |
rs748501234 | in-del | -/TGAG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699376 | GTGTGTGTGTGTGTG[-/TGAG]AGAGAGAGAGAGAGA | 9870 |
rs748530692 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665197 | TACCTGGGACCTCTA[A/C]ATCTGAATCTCTCGG | 9870 |
rs748566910 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679231 | AAGAAAAGCTCAGCC[C/T]GAGCAACATGGCAAA | 9870 |
rs748694852 | snp | C/T | 1.68772e-05 | 0.00290488 | intron-variant | AREL1 | GRCh38.p7 | 14:74683584 | CAGAGGAAAAAAACA[C/T]TTCCTGTGTAGAGTG | 9870 |
rs748714324 | snp | C/T | 1.66499e-05 | 0.00288525 | missense | AREL1 | GRCh38.p7 | 14:74667509 | ACTTGACTGGCCAGC[C/T]GATATTGGGCCAGCA | 9870 |
rs748726321 | snp | A/T | 1.66832e-05 | 0.00288814 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713548 | AGTCTCAGAGATCAG[A/T]GGCTGTGAGTGTCTG | 9870 |
rs748731246 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703650 | TTAGATTCATACATG[C/T]TGTTACACATTTCGG | 9870 |
rs748782547 | snp | A/G | 4.98633e-05 | 0.00499291 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670851 | CAAACCATTCCCGGC[A/G]AGGCCCTCCCCAGTC | 9870 |
rs748847696 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683972 | CTCTCAAGCCAAGCT[C/T]AATGCTACAGTGGAG | 9870 |
rs748852378 | snp | C/T | 0.000188164 | 0.00969777 | intron-variant | AREL1 | GRCh38.p7 | 14:74678234 | GTGTGACTTGGCTCA[C/T]GCCTGTAATCCCAAC | 9870 |
rs748854360 | snp | A/G | 1.65647e-05 | 0.00287786 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672939 | CACCTTGTCCTGAAA[A/G]GTCTCAGAGCCTCCT | 9870 |
rs748904839 | snp | C/T | 1.66757e-05 | 0.00288749 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669641 | AGAGGCTTTGTCCTC[C/T]TTCTCACCTTATCCA | 9870 |
rs748964367 | in-del | -/AAAT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694179 | ACCCAGTCTCAAAAT[-/AAAT]AAATAAATAAATAAA | 9870 |
rs748974195 | snp | C/T | 0.00144733 | 0.026862 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712916 | GGGCTCTGCCTAAGG[C/T]TGGAGAGAAACGTTA | 9870 |
rs749082774 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696503 | GTTGCTAAAATTACT[A/C]TAACACATACTACTA | 9870 |
rs749096493 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701629 | ACACAGCCAAACCAT[A/G]TCATTCCACCCCGGC | 9870 |
rs749115319 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669100 | GGTCTTGCCAAAGTT[A/G]CCCAGGCTGGTCTTG | 9870 |
rs749136721 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695632 | GAATCAGCCACTTCC[C/T]CCTTTGTGGTGCTCC | 9870 |
rs749240109 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672241 | AGTAGATTTGAAGGC[A/C]AGTAAGTAAACTGCT | 9870 |
rs749265768 | snp | C/T | 3.31323e-05 | 0.00407002 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676716 | ACAAGAGTAGAAAAG[C/T]GGCACACAATTTTGG | 9870 |
rs749285374 | snp | A/G | 3.34739e-05 | 0.00409095 | missense | AREL1 | GRCh38.p7 | 14:74664020 | TGAACTGAAGTAGCC[A/G]AGCCAACTCCTCCTG | 9870 |
rs749313742 | snp | A/T | 1.74515e-05 | 0.00295389 | intron-variant | AREL1 | GRCh38.p7 | 14:74674116 | ACTGAGAATTGCTGG[A/T]GGACCAACAGACAGG | 9870 |
rs749373386 | snp | A/G | 1.67086e-05 | 0.00289033 | intron-variant | AREL1 | GRCh38.p7 | 14:74683568 | GACACCTGTTAGCAA[A/G]CAGAGGAAAAAAACA | 9870 |
rs749407850 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698859 | TGAGATCCCATCTCT[-/AA]AAAAAAAAAAAAAAA | 9870 |
rs749433591 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674902 | GGGTGAGCTGGAGTG[A/G]AATATGTTGGTGGTA | 9870 |
rs749463932 | in-del | -/AGAAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680217 | AAAAGAAAAGAAAAG[-/AGAAA]AGAAAAGAAAAGAAA | 9870 |
rs749489632 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702056 | GCCTCCTCCCCAGCT[A/G]CTTTCGTGGGCTAGC | 9870 |
rs749526459 | snp | A/G | 1.65649e-05 | 0.00287788 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675748 | TTCTTCACCTTCTCA[A/G]GGGTGTGGCACTCAG | 9870 |
rs749594942 | snp | G/T | 1.65075e-05 | 0.00287289 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713111 | AGTTTCCGCTTCCGG[G/T]CTATCCTTTGCCGGA | 9870 |
rs749620849 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674682 | TGTAATACTCAAGTC[-/T]TTCTAAATATCTGGG | 9870 |
rs749626305 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667198 | GAGCGACAAAAGTGA[A/G]ACCACCTCTTGCATA | 9870 |
rs749631696 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711806 | ACCCAATGTCATGGC[A/G]AGTTATAAGGCAGAG | 9870 |
rs749631834 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700896 | AGAAAAAGGATCACA[C/T]ATTTTAAATGAAGTA | 9870 |
rs749656235 | snp | A/T | 1.66338e-05 | 0.00288386 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671422 | CCTTCTTCATCCTGG[A/T]AAACAACCTCAAAGT | 9870 |
rs749770219 | snp | C/T | 3.31807e-05 | 0.00407299 | intron-variant | AREL1 | GRCh38.p7 | 14:74672806 | AAACTTTGGTATCTG[C/T]TGACAGAGATGAAAT | 9870 |
rs749811926 | snp | A/G | 1.66527e-05 | 0.00288549 | intron-variant | AREL1 | GRCh38.p7 | 14:74667310 | GGAGTCTGAATTGCA[A/G]TCACTTACCTCAAGC | 9870 |
rs749833084 | snp | A/G | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713166 | TATTGCGCCGTTGGT[A/G]ATTACGGAAGAACCA | 9870 |
rs749909711 | snp | C/T | 4.97376e-05 | 0.00498662 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670811 | AGCTGATTGGTGGTA[C/T]CAAATAGTGCTTTGC | 9870 |
rs749936810 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706253 | TGAACCTGACAAGCC[A/G]TCTCCCTCAATAAGT | 9870 |
rs749959757 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707080 | TATCAAAATTATACA[C/T]GATCTGGTCGGGCAC | 9870 |
rs750010199 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686460 | GTATGCTAACGTTCA[C/T]ATCTTATCACTGAGT | 9870 |
rs750045615 | snp | A/G | 1.71355e-05 | 0.00292702 | intron-variant | AREL1 | GRCh38.p7 | 14:74683276 | AGACAAAGGGAAAAA[A/G]AAAGGAAAAAAGAAC | 9870 |
rs750091490 | snp | A/T | 9.0086e-05 | 0.0067108 | intron-variant | AREL1 | GRCh38.p7 | 14:74676796 | TTATTTATTTTATTT[A/T]TTTATTTTTATTTTT | 9870 |
rs750101037 | snp | C/T | 2.03801e-05 | 0.00319212 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713070 | CGGCCTGGGAACCGG[C/T]TCGGGGGATTGCCCT | 9870 |
rs750111677 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673363 | GAAATACATTTCATT[A/T]TTTTTCCCTTCAGTG | 9870 |
rs750131819 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694737 | GCTCACGCCTGTAAT[-/C]CCAGCACTTTGGGAG | 9870 |
rs750154650 | snp | C/T | 1.6908e-05 | 0.00290753 | intron-variant | AREL1 | GRCh38.p7 | 14:74664793 | GAAACTTTTTCCTTA[C/T]AACATGGCACAAATC | 9870 |
rs750165282 | snp | C/T | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713180 | TGATTACGGAAGAAC[C/T]AGGAGTTTGGCGTGA | 9870 |
rs750198630 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699027 | GACTCTGTCTCCAAA[A/G]AAAACCAAGGTGTTT | 9870 |
rs750212930 | snp | A/G | 1.66172e-05 | 0.00288242 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675714 | CTTTGGTGACACATA[A/G]CAGTACACCTTCTTC | 9870 |
rs750224170 | snp | G/T | 0.000563558 | 0.0167768 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684485 | ATGCTGTGGCCCACC[G/T]CATAGGGGTCCTTCC | 9870 |
rs750277583 | snp | A/G | 3.38175e-05 | 0.00411189 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | AREL1, FCF1 | GRCh38.p7 | 14:74713490 | CTGTTTCAAGGGGAA[A/G]CAAAAGAAAACAAGG | 9870 |
rs750286531 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700481 | TTAAGCTCAGAAATA[C/T]TTAATTTGAAATTTT | 9870 |
rs750319173 | snp | C/T | 3.31813e-05 | 0.00407302 | intron-variant | AREL1 | GRCh38.p7 | 14:74670178 | TTTCTTCAAGCCCAG[C/T]TCTGGAAGGACCCTT | 9870 |
rs750330046 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678878 | CATAAAAGAAAAAAA[C/T]GGATGCACTGGATTT | 9870 |
rs750336391 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711810 | AATGTCATGGCGAGT[C/T]ATAAGGCAGAGCAAG | 9870 |
rs750372619 | snp | A/T | 4.96907e-05 | 0.00498426 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675834 | GGTCATGTGCATGGG[A/T]GGCAGGTGCCATGGA | 9870 |
rs750437436 | snp | C/T | 9.94019e-05 | 0.00704919 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676616 | GTAATTGTGCTCATC[C/T]CTCAAGGACATGGAA | 9870 |
rs750439095 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691597 | ATGTCAAAGAAAAGT[A/G]GAATGCAATGCCAAT | 9870 |
rs750465643 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666793 | GGTGCGATCTCGGAT[C/T]ACTGCAACTTCCGCC | 9870 |
rs750480931 | snp | A/G | 1.65963e-05 | 0.0028806 | intron-variant | AREL1 | GRCh38.p7 | 14:74672785 | GAATATAGACATTCA[A/G]TTGGAAAACTTTGGT | 9870 |
rs750572804 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692831 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 9870 |
rs750600380 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671740 | AAGTTGTTTTTTTCT[C/T]TTCCTTTTGTTTTAA | 9870 |
rs750603823 | snp | C/T | 6.6538e-05 | 0.00576755 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667487 | GAAATGTTCCACCTC[C/T]TCTTTCACTTGACTG | 9870 |
rs750637201 | snp | C/T | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713215 | GGTGAGAGAAGACGG[C/T]CCAAGAAGGGACGTT | 9870 |
rs750664861 | snp | C/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672880 | GTGACTTTGGAATGT[C/G]GTCTTTTCATATGTA | 9870 |
rs750730339 | snp | A/G | 1.65743e-05 | 0.00287869 | intron-variant | AREL1 | GRCh38.p7 | 14:74667395 | GAAACAAAGTAGGCA[A/G]GTTAAAGTCATACCC | 9870 |
rs750880643 | snp | A/G | 1.65597e-05 | 0.00287743 | intron-variant | AREL1 | GRCh38.p7 | 14:74663838 | CTGGAAGGGCAAGGG[A/G]GAAGTGATTAACTCA | 9870 |
rs750889105 | snp | A/G | 3.36819e-05 | 0.00410364 | intron-variant | AREL1 | GRCh38.p7 | 14:74676340 | TAGGAAGGCAACAGA[A/G]CATCACTTAACATAT | 9870 |
rs750895642 | snp | A/G | 1.65677e-05 | 0.00287812 | stop-gained, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676237 | AATGCAGGGTGAGTC[A/G]CAAGAACACCTGGAA | 9870 |
rs750896343 | in-del | -/AG | 1.6588e-05 | 0.00287988 | intron-variant | AREL1 | GRCh38.p7 | 14:74672811 | TTGGTATCTGCTGAC[-/AG]AGATGAAATTTTACC | 9870 |
rs750931453 | snp | A/G | 1.66294e-05 | 0.00288347 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685607 | TAACGTACCAATAAC[A/G]TAAAACATCAGGTCC | 9870 |
rs750961800 | snp | C/T | 1.65605e-05 | 0.0028775 | missense | AREL1 | GRCh38.p7 | 14:74663726 | GGAGAGTGGTCAGAG[C/T]ATGCCAAAGCCCTCG | 9870 |
rs751056919 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708578 | CTGGATAAAAGCAAG[A/G]GGACATTACAGAAAA | 9870 |
rs751061016 | snp | A/G | 0.000132481 | 0.00813775 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675809 | CAGTGGATGGCCGGC[A/G]CTGGGAAGAGGTCAT | 9870 |
rs751096628 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709657 | CTGTATGCCATGCTA[C/T]CACATTTAGGGGCAG | 9870 |
rs751120056 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662742 | CTGCCAGAGAACACC[A/C]AGCAGAGAGAGAATC | 9870 |
rs751158732 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674386 | AGGCAGATCACTTGA[G/T]GCCAGGAGTTCAAGA | 9870 |
rs751212708 | in-del | -/AAAGA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680198 | AAGAAAAAAAGAAAG[-/AAAGA]AAAGAAAAGAAAAGA | 9870 |
rs751229273 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700040 | GCAAGTGAGGAAGAT[A/G]GCTTCAATCTACCTG | 9870 |
rs751230740 | snp | A/C | 0.00101368 | 0.0224903 | intron-variant, utr-variant-5-prime | AREL1 | GRCh38.p7 | 14:74698791 | CACTTTGGGAGGCTG[A/C]GGTGGGAGGATGGCT | 9870 |
rs751244581 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661806 | CTGAAAAAGTGCTAT[A/G]ACTAGAGCTTAAAAT | 9870 |
rs751248662 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675493 | ATCACAGAACAAAAG[A/T]TCAAATTGTTTTGAC | 9870 |
rs751278350 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701809 | TTAGTTACTTTCTAG[A/G]TACAATGGGAGTACA | 9870 |
rs751294093 | snp | A/C | 1.81352e-05 | 0.00301119 | intron-variant | AREL1 | GRCh38.p7 | 14:74670158 | CTGAAAGGCCCTGGG[A/C]CATTTTTCTTCAAGC | 9870 |
rs751334545 | snp | C/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713399 | ATTTGAGGCAAGAAG[C/G]GAAGGCAATAGACAA | 9870 |
rs751345555 | snp | A/G | 1.6588e-05 | 0.00287988 | missense | AREL1 | GRCh38.p7 | 14:74667362 | AAAAGGTTCTCAGGG[A/G]CCAATTCATTCAGGC | 9870 |
rs751346044 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681473 | GGGTTGCCAGGGGTT[A/G]AGAACAGGTTGGGGA | 9870 |
rs751347586 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686713 | TGCTTAGTTCCTCTG[A/G]TAACAATATACCCAG | 9870 |
rs751354909 | snp | C/G | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713210 | ACCATGGTGAGAGAA[C/G]ACGGTCCAAGAAGGG | 9870 |
rs751380411 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687771 | TGATTATTACAATTA[C/T]TATCAATAGTAGCGC | 9870 |
rs751407938 | snp | C/T | 1.64741e-05 | 0.00286998 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713145 | AGTATGTGAATGACG[C/T]AGAAGTATTGCGCCG | 9870 |
rs751413375 | snp | C/T | 1.67767e-05 | 0.00289622 | intron-variant | AREL1 | GRCh38.p7 | 14:74675695 | CGAGAATGGAAGGTC[C/T]AACCTTTGGTGACAC | 9870 |
rs751428855 | in-del | -/CT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682785 | CAGCACCTCCTCCCT[-/CT]CTCTCTCTCTCTTGC | 9870 |
rs751455935 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684057 | TTTGGCTTTGTGGAC[C/T]GTACACAACTACTCA | 9870 |
rs751463684 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700636 | ACAAAAAAAATTAGC[C/T]GGGCATGGTGGCACA | 9870 |
rs751493440 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714512 | CCCCCAAAAGTTAAA[A/G]CATCTGAATCTTCAG | 9870 |
rs751504568 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667889 | ATACTATGGCTCCTC[A/G]CTAGCAATGTTTTAA | 9870 |
rs751643729 | snp | C/T | | | synonymous-codon, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669658 | TCTCACCTTATCCAA[C/T]TGACCTGATTTATTA | 9870 |
rs751659608 | snp | G/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661030 | ACACTTGTCCTCGTC[G/T]CCCCATGGCTGAGAC | 9870 |
rs751661737 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693439 | CCAAAAATGTAGCAG[A/G]AAGGGGGTTTATGGC | 9870 |
rs751662342 | snp | C/T | 1.65611e-05 | 0.00287755 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663717 | TGGATGACAGGAGAG[C/T]GGTCAGAGCATGCCA | 9870 |
rs751705418 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680300 | CAGACAGGCACATGA[A/G]AAGATGTTCAATAGC | 9870 |
rs751719515 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693093 | GGTTGCAGCACAGGG[C/T]CTGGAGCAACCACAA | 9870 |
rs751790388 | snp | C/T | 0.000188023 | 0.00969413 | intron-variant | AREL1 | GRCh38.p7 | 14:74671968 | TTCCAGTCACACCTA[C/T]CAGAGCCAAACATCA | 9870 |
rs751824519 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676607 | GGACAAGGTGTAATT[A/G]TGCTCATCTCTCAAG | 9870 |
rs751837144 | snp | A/G | 1.6649e-05 | 0.00288518 | intron-variant | AREL1 | GRCh38.p7 | 14:74673222 | AAGGTATGAAAACTG[A/G]TAAAGAAAAACAAAG | 9870 |
rs751868063 | in-del | -/ATTAT | 1.7725e-05 | 0.00297694 | intron-variant | AREL1 | GRCh38.p7 | 14:74684700 | CAAAAGAGAGAACAC[-/ATTAT]ACAAACCGCCTGCCA | 9870 |
rs751890026 | snp | C/T | 1.7119e-05 | 0.00292562 | intron-variant | AREL1 | GRCh38.p7 | 14:74671388 | GTTCAAAAAGATGAA[C/T]ATAAAATTTCAAAAC | 9870 |
rs751899073 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704387 | GGAGACTTGAGACAT[C/G]AATCAAGATGTATAC | 9870 |
rs751946800 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677100 | CACCACGCCCGGCTG[C/G]AATCTAACATTTAAA | 9870 |
rs752007882 | in-del | -/G | 1.66416e-05 | 0.00288453 | intron-variant | AREL1 | GRCh38.p7 | 14:74673221 | CAAGGTATGAAAACT[-/G]GTAAAGAAAAACAAA | 9870 |
rs752015115 | snp | C/T | 1.66034e-05 | 0.00288122 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684610 | CTGGAGGAAGCTGAC[C/T]ACACGTGCGGCAAGC | 9870 |
rs752036105 | snp | C/T | 1.69991e-05 | 0.00291535 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669960 | ACCTTGTAATGCATA[C/T]GCAGTCCTATGATTT | 9870 |
rs752057796 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670511 | AATTATTATAATAAT[C/T]AGTAGAGTAGACATT | 9870 |
rs752059529 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684843 | CTGTAGATAAGAAAG[A/G]AACTTCTACACCAGG | 9870 |
rs752060577 | snp | C/G | 1.77846e-05 | 0.00298194 | intron-variant | AREL1 | GRCh38.p7 | 14:74684702 | AAAAGAGAGAACACA[C/G]AAACCGCCTGCCAGT | 9870 |
rs752116517 | snp | A/C | 1.65729e-05 | 0.00287857 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669741 | TAAAACAAACTTTAG[A/C]TTTGTAGAATTCTGG | 9870 |
rs752131409 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671903 | TATCCACAAGGCTAG[A/G]TTCAGACAGCGAGCC | 9870 |
rs752196911 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662249 | CCTCATGATCCCTGC[A/G]AACAGGAGGGCTCAG | 9870 |
rs752203284 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698373 | GGCTTCTAGAACATT[C/G]TTGCCTGCCCTGATG | 9870 |
rs752216246 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697510 | CTCTTAGTTTATACT[C/T]CCCAACCCAAAATCC | 9870 |
rs752340920 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710095 | TTTCTGCTCCCATCC[A/C]TCACAAATCAACACT | 9870 |
rs752377833 | snp | G/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663568 | TGAGGTAAAGACAAG[G/T]CTTGTAGGTGACAAA | 9870 |
rs752434275 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662701 | TAAGCACGTAAACTC[C/T]TAGTCCCTGTTCCTT | 9870 |
rs752436167 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708867 | AATACCCATCTTTCT[C/G]TATAAACCCTATCTT | 9870 |
rs752457056 | snp | A/G | 5.10643e-05 | 0.00505268 | intron-variant | AREL1 | GRCh38.p7 | 14:74675681 | GGGGGATTTTATGTC[A/G]AGAATGGAAGGTCCA | 9870 |
rs752460182 | snp | A/G | 1.66776e-05 | 0.00288765 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669991 | GGGCCAGGAAAGAGC[A/G]GGTGAAGCGAGCTCG | 9870 |
rs752520106 | snp | A/C | 1.66012e-05 | 0.00288103 | missense | AREL1 | GRCh38.p7 | 14:74667345 | TCTCATCAAAAATAG[A/C]CAAAAGGTTCTCAGG | 9870 |
rs752522794 | snp | A/G | 3.51315e-05 | 0.004191 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713081 | CCGGCTCGGGGGATT[A/G]CCCTTTCCCCAAGGA | 9870 |
rs752530354 | snp | C/T | 4.96808e-05 | 0.00498377 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683406 | GCCACTTTTACTACG[C/T]TGGAATTGGGCTCCT | 9870 |
rs752599769 | in-del | -/AA/AAA | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712058 | AAAAAAAAAAAAAAA[-/AA/AAA]AAAAAAAAAGAAAAA | 9870 |
rs752619996 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678055 | TTAACACAATTCTTA[A/T]CAAAGTTCCAGCAAG | 9870 |
rs752635814 | snp | A/C | 1.64746e-05 | 0.00287002 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713138 | CGGAAGCAGTATGTG[A/C]ATGACGTAGAAGTAT | 9870 |
rs752636254 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702905 | AATTCCTCATCTCCA[A/T]CTGAGACCACCTCAG | 9870 |
rs752682337 | snp | C/G/T | 8.28362e-05 | 0.00643522 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683327 | GTAGTAGGGACTATA[C/G/T]GCCACATTTAATCCA | 9870 |
rs752685748 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687195 | GCAAAGAAATGAAGT[A/G]TATGTGGCTGGTGTT | 9870 |
rs752749369 | snp | A/G | 1.66682e-05 | 0.00288684 | intron-variant | AREL1 | GRCh38.p7 | 14:74664954 | GTAAGGTGTTACTAT[A/G]ACAGTCAGAGAGACA | 9870 |
rs752799588 | snp | A/C | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714645 | TACTCATTAACAATT[A/C]TTATGCATTATTGGC | 9870 |
rs752811143 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669044 | AGGACCACAGGCACA[C/T]GCCACCATACCCAGC | 9870 |
rs752822149 | snp | A/T | 4.97599e-05 | 0.00498773 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684587 | CCTCGGCGCTCGCGG[A/T]CCTCATTCTGGAGGA | 9870 |
rs752826616 | snp | C/T | 1.6617e-05 | 0.00288239 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670847 | AGCTCAAACCATTCC[C/T]GGCGAGGCCCTCCCC | 9870 |
rs752848018 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680700 | AGACCACAGAATATA[C/T]GTAGAGAATCCCTAA | 9870 |
rs752861745 | snp | G/T | 5.75854e-05 | 0.00536558 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714833 | TAATTGCTGTGGTTT[G/T]TCTTCTCCCTTGGAT | 9870 |
rs752874958 | in-del | -/AGAG | 1.66638e-05 | 0.00288645 | intron-variant | AREL1 | GRCh38.p7 | 14:74685575 | TTACAAAAATATAAT[-/AGAG]AGAGCTCTTTCCATA | 9870 |
rs752881821 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668253 | CCCCCAATAAACTCC[G/T]AAGGGAACTTTGAAG | 9870 |
rs752936094 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682176 | GGAAAGAGAGACGGC[C/T]TGAGAGCCACTTTGT | 9870 |
rs752977845 | snp | G/T | 2.11965e-05 | 0.00325543 | intron-variant | AREL1 | GRCh38.p7 | 14:74676785 | GAATCTAACATTTAT[G/T]TATTTTATTTTTTTA | 9870 |
rs752981671 | snp | A/C/G | 3.62939e-05 | 0.0042598 | intron-variant | AREL1 | GRCh38.p7 | 14:74675986 | TTAAAGTAGAAGTCA[A/C/G]AGAAGAAAAAAATTA | 9870 |
rs752983354 | snp | A/T | 3.36033e-05 | 0.00409884 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684664 | GAAGAATGCAACCAC[A/T]GACACTGTGATTCCA | 9870 |
rs753032344 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672898 | CTTTTCATATGTACC[C/T]GCCGAAGCTCTCGCT | 9870 |
rs753087165 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674826 | CACCAGCAACCCATA[C/G]ACACTGCTTTATACC | 9870 |
rs753108549 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705227 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 9870 |
rs753130346 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694158 | CCACCCTGGGCAACA[A/G]AGCCAGACCCAGTCT | 9870 |
rs753166070 | snp | A/G | 1.66879e-05 | 0.00288855 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713518 | AGGAAGTATGCGACC[A/G]TGAAGCGAATGCTTA | 9870 |
rs753261124 | snp | C/T | 1.65814e-05 | 0.00287931 | intron-variant | AREL1 | GRCh38.p7 | 14:74673047 | GGCTGGGCTCACTAC[C/T]TTCCCTATAGAATCC | 9870 |
rs753280566 | in-del | -/A | 2.10338e-05 | 0.00324291 | intron-variant | AREL1 | GRCh38.p7 | 14:74670923 | CTCCCTCCTCTTACC[-/A]CTTTTGTTTATTGAG | 9870 |
rs753335684 | snp | A/G | 1.86294e-05 | 0.00305195 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713075 | TGGGAACCGGCTCGG[A/G]GGATTGCCCTTTCCC | 9870 |
rs753362895 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685152 | GCAGTCAAAAGGATG[C/T]GCCTTTGGTTCCCAC | 9870 |
rs753372086 | snp | C/T | 1.66571e-05 | 0.00288587 | intron-variant | AREL1 | GRCh38.p7 | 14:74664950 | GATGGTAAGGTGTTA[C/T]TATGACAGTCAGAGA | 9870 |
rs753393793 | snp | C/G | 1.66843e-05 | 0.00288823 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683296 | GAAAAAAGAACCTAC[C/G]AGGTTGAAAAATTTT | 9870 |
rs753487458 | snp | C/G | 1.66134e-05 | 0.00288208 | intron-variant | AREL1 | GRCh38.p7 | 14:74669784 | AAAGTACTGAGGAGG[C/G]AGAAAGACACAGAAC | 9870 |
rs753498137 | snp | C/T | 1.69876e-05 | 0.00291436 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674041 | CAGCTTACTTTTGTT[C/T]CTGGACACACTCGGA | 9870 |
rs753551233 | snp | A/T | 3.34773e-05 | 0.00409115 | intron-variant | AREL1 | GRCh38.p7 | 14:74673235 | TGGTAAAGAAAAACA[A/T]AGAAATTAATCTATA | 9870 |
rs753557283 | snp | C/G | 1.65603e-05 | 0.00287747 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683395 | GCACAGTGAAGGCCA[C/G]TTTTACTACGTTGGA | 9870 |
rs753595177 | snp | G/T | 1.75792e-05 | 0.00296467 | intron-variant | AREL1 | GRCh38.p7 | 14:74670726 | CTACCCATGATAACA[G/T]AATCCACATTTTCCA | 9870 |
rs753612252 | snp | A/G | 1.65592e-05 | 0.00287738 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663732 | TGGTCAGAGCATGCC[A/G]AAGCCCTCGCAACCC | 9870 |
rs753619942 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710358 | AGAAATTACAAATGG[A/C]CTTTTTTTAAGTTGT | 9870 |
rs753638229 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697598 | TGTCTATTTCTGCTA[C/T]TGTGGTTTAGCCAAG | 9870 |
rs753638241 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711499 | TGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAA | 9870 |
rs753827398 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670826 | TCAAATAGTGCTTTG[C/T]AGATTAGCTCAAACC | 9870 |
rs753842281 | snp | G/T | 5.82004e-05 | 0.00539415 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713043 | CAACAGACCCCAGAG[G/T]TGGTCTCCACCCGGC | 9870 |
rs753844504 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant | AREL1 | GRCh38.p7 | 14:74673032 | CACCCTCATGGATGT[A/G]GCTGGGCTCACTACC | 9870 |
rs753849175 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74676849 | TCGCCCAGGCTGGAG[C/T]GCAGTGGCGCAATCT | 9870 |
rs753949432 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683175 | GTATACTTTAAAAGG[A/G]TGAATTTTATGGCAT | 9870 |
rs753952174 | snp | A/G | 6.70657e-05 | 0.00579037 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | AREL1, FCF1 | GRCh38.p7 | 14:74713502 | GAAGCAAAAGAAAAC[A/G]AGGAAGTATGCGACC | 9870 |
rs753955300 | snp | C/T | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675851 | GCAGGTGCCATGGAG[C/T]GCTGCTACAGTTGGT | 9870 |
rs754000076 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669180 | AATTACAGGCCATGA[A/G]CCACTGCGCCCAGCC | 9870 |
rs754009567 | snp | A/G | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713235 | GAAGGGACGTTATCA[A/G]GCCACTTTTTGGGTG | 9870 |
rs754078549 | snp | C/T | 1.77893e-05 | 0.00298234 | intron-variant | AREL1 | GRCh38.p7 | 14:74667644 | GCTGTGGATGGAAAT[C/T]TATGAGATGACATCT | 9870 |
rs754196201 | snp | A/T | 8.66303e-05 | 0.00658086 | intron-variant | AREL1 | GRCh38.p7 | 14:74676370 | TAGTATTTTCCCATT[A/T]ACAAGCCACTTTACT | 9870 |
rs754200711 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695914 | AAGGGGCTCAACATT[C/T]TGTATCTCTAACAGG | 9870 |
rs754222704 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699767 | CAAGAACCTATCAAC[A/G]TCAAGTGAGGACTTG | 9870 |
rs754252343 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694564 | ACCTGTACCTTTTAG[C/T]GTTTTTCAAATTCTT | 9870 |
rs754295042 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682408 | ATAAAAACATGTCAA[C/T]ACAAAAACTTGTACA | 9870 |
rs754333648 | snp | C/G/T | 4.96827e-05 | 0.0049839 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672892 | TGTGGTCTTTTCATA[C/G/T]GTACCTGCCGAAGCT | 9870 |
rs754357810 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676659 | TTATCATACTCATCT[C/T]GGGGTACTATTTGAA | 9870 |
rs754555326 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697320 | TTTTGTAAGATGCAA[C/T]CTCCAGCATTCTCCA | 9870 |
rs754567914 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682600 | TGGTTTAGATATTTG[C/T]ACCCTCCAAATCGCA | 9870 |
rs754576951 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661868 | TCCAGGATCAGTCTC[C/T]GGAAGGCTGCCGGAG | 9870 |
rs754592437 | snp | A/G | 1.65935e-05 | 0.00288036 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683314 | GTTGAAAAATTTTGT[A/G]GTAGGGACTATATGC | 9870 |
rs754605875 | snp | A/G | 1.6623e-05 | 0.00288292 | intron-variant | AREL1 | GRCh38.p7 | 14:74669798 | GCAGAAAGACACAGA[A/G]CAGAACATGAATACT | 9870 |
rs754627284 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707124 | TATAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 9870 |
rs754644826 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708679 | TGTTAACTATTGGCA[C/T]CTCAACAGTAACAAG | 9870 |
rs754668964 | snp | A/G | 2.69393e-05 | 0.00367 | upstream-variant-2KB, missense, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714907 | AACCTAAAAAGAAAG[A/G]AAAGAAGGATCCCAG | 9870 |
rs754679408 | snp | A/G | 2.80328e-05 | 0.00374374 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713046 | CAGACCCCAGAGTTG[A/G]TCTCCACCCGGCCTG | 9870 |
rs754713908 | snp | A/G | 1.67503e-05 | 0.00289393 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664021 | GAACTGAAGTAGCCG[A/G]GCCAACTCCTCCTGG | 9870 |
rs754754855 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673557 | TATTAAACAGCAATA[A/T]ATGACTACTCCAAAC | 9870 |
rs754798194 | snp | A/T | 1.79812e-05 | 0.00299838 | intron-variant | AREL1 | GRCh38.p7 | 14:74675965 | AAGTATAATAAGGAA[A/T]AAGGTTTAAAGTAGA | 9870 |
rs754864761 | snp | A/G | 1.73751e-05 | 0.00294742 | intron-variant | AREL1 | GRCh38.p7 | 14:74670734 | GATAACATAATCCAC[A/G]TTTTCCACCCACCCG | 9870 |
rs754990098 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701883 | AAAACAAAGGGGCTG[C/T]AGGGCCCATGCAAGT | 9870 |
rs755011831 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680317 | AGATGTTCAATAGCA[C/T]TAACTATTTAAGAAA | 9870 |
rs755014231 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709330 | ATAAAATCTGATCTA[C/T]TACATGGTACTAATA | 9870 |
rs755015695 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668114 | TCTCAGCCCTGATGC[C/T]AGCTTGCTACAGACC | 9870 |
rs755018830 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685037 | ATATTTACTCTCTGG[C/T]CTTTTATAGAAAAAG | 9870 |
rs755051038 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713309 | TCCTAGCATATTTTC[A/G]TTCTGGTCTTAGCTC | 9870 |
rs755056755 | snp | A/C | 3.32989e-05 | 0.00408024 | missense | AREL1 | GRCh38.p7 | 14:74667499 | CTCCTCTTTCACTTG[A/C]CTGGCCAGCCGATAT | 9870 |
rs755067432 | snp | C/T | 3.31466e-05 | 0.0040709 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684516 | AATCCCAGGAGACTT[C/T]GCAAGACCGGGGATC | 9870 |
rs755126097 | in-del | -/AAAC | 3.33303e-05 | 0.00408216 | intron-variant | AREL1 | GRCh38.p7 | 14:74673230 | AAAACTGGTAAAGAA[-/AAAC]AAAGAAATTAATCTA | 9870 |
rs755202816 | snp | C/T | 1.65809e-05 | 0.00287926 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675859 | CATGGAGTGCTGCTA[C/T]AGTTGGTAGCATTAT | 9870 |
rs755255102 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668486 | TTTTTTTTAATGTAA[A/G]CATTTCTATCTAGGA | 9870 |
rs755270716 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676670 | ATCTCGGGGTACTAT[C/T]TGAAGGGTGTGCGGC | 9870 |
rs755280699 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679114 | TATGTTGCCCAGGCC[A/G]GTCTTGAACTCCTGG | 9870 |
rs755332567 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677363 | TTAGCCAGGCATGGT[A/G]GTTCATGCCTGTGTC | 9870 |
rs755429488 | snp | A/T | 0.000328893 | 0.0128195 | intron-variant | AREL1 | GRCh38.p7 | 14:74692360 | ACAGGGTTAGTTGGA[A/T]TAGGTTTTTATTTCT | 9870 |
rs755429571 | in-del | -/ACCGCC | 1.77995e-05 | 0.00298319 | intron-variant | AREL1 | GRCh38.p7 | 14:74684705 | AGAGAGAACACACAA[-/ACCGCC]TGCCAGTTACACATT | 9870 |
rs755441462 | snp | A/C | 1.65605e-05 | 0.0028775 | intron-variant | AREL1 | GRCh38.p7 | 14:74663850 | GGGAGAAGTGATTAA[A/C]TCATACCACCAAAAA | 9870 |
rs755481163 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669154 | CTGCCTCAGCCTCCC[-/A]AAAGTGTTGCAATTA | 9870 |
rs755562273 | snp | A/G | 3.37519e-05 | 0.00410789 | intron-variant | AREL1 | GRCh38.p7 | 14:74664797 | CTTTTTCCTTATAAC[A/G]TGGCACAAATCCAAC | 9870 |
rs755570158 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683911 | CCGGCAGCACTGGCA[A/G]TGAGTGAACTAAAGC | 9870 |
rs755590003 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671913 | GCTAGGTTCAGACAG[C/T]GAGCCATGCCACACG | 9870 |
rs755643730 | snp | C/T | 4.47077e-05 | 0.00472778 | intron-variant | AREL1 | GRCh38.p7 | 14:74676797 | TATTTATTTTATTTT[C/T]TTATTTTTATTTTTT | 9870 |
rs755677403 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684989 | ACTACACTGGCAGAG[C/T]TGAGTCATTGAAATG | 9870 |
rs755695104 | snp | A/C | 2.96169e-05 | 0.00384806 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713041 | ACCAACAGACCCCAG[A/C]GTTGGTCTCCACCCG | 9870 |
rs755707418 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685402 | GACTCCACAGTAAAC[-/A]AGTGTCTGGCATTGA | 9870 |
rs755746036 | snp | C/T | 3.31235e-05 | 0.00406948 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676685 | TTGAAGGGTGTGCGG[C/T]TGCCCACAGGTCAAT | 9870 |
rs755838503 | snp | C/T | 1.69172e-05 | 0.00290832 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670092 | TCATACATTTTCAGG[C/T]GCAGATGAGCGGGGC | 9870 |
rs755846377 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662041 | CATTTGGGCAAGCAG[C/T]AGCACCTTGTCCTGG | 9870 |
rs755876719 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708882 | CTATAAACCCTATCT[A/T]GTAGAACAGTCTTCA | 9870 |
rs755892782 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690266 | AAGACCCTGTCTCCA[-/AA]AAAAAAAAAAAAAAA | 9870 |
rs755919486 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675646 | TGCTACCAAATACCA[A/G]TTACACACAGGTTCA | 9870 |
rs755959741 | snp | A/G | 1.65979e-05 | 0.00288074 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675719 | GTGACACATAGCAGT[A/G]CACCTTCTTCGGTTT | 9870 |
rs756093138 | snp | C/T | 0.000712674 | 0.0188634 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712899 | GTAAAGGCAGGTCTT[C/T]TGGGCTCTGCCTAAG | 9870 |
rs756146101 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701201 | AAGGAAAAAGGCAAA[A/T]TTTCTATGGTTGGGA | 9870 |
rs756167066 | snp | G/T | 3.29484e-05 | 0.00405871 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713228 | GGTCCAAGAAGGGAC[G/T]TTATCAGGCCACTTT | 9870 |
rs756182276 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669059 | CGCCACCATACCCAG[A/C]TAGATTTTTAAAATC | 9870 |
rs756201444 | snp | A/G | 3.31472e-05 | 0.00407093 | intron-variant | AREL1 | GRCh38.p7 | 14:74667396 | AAACAAAGTAGGCAA[A/G]TTAAAGTCATACCCA | 9870 |
rs756207714 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702030 | CCATCCCTGTGGCTT[C/T]GCAGGGTACAGCCTC | 9870 |
rs756210645 | snp | A/T | 1.65954e-05 | 0.00288053 | intron-variant | AREL1 | GRCh38.p7 | 14:74672793 | ACATTCAATTGGAAA[A/T]CTTTGGTATCTGCTG | 9870 |
rs756257332 | snp | C/T | 1.84544e-05 | 0.00303758 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713441 | AGACTTTAAAAGATG[C/T]CGTGTGTTTCCAACT | 9870 |
rs756280908 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687913 | GTCCCTGAACAGTCT[A/G]CATGGGAGTTCTTTA | 9870 |
rs756324506 | snp | C/T | 1.66649e-05 | 0.00288655 | intron-variant | AREL1 | GRCh38.p7 | 14:74683559 | GAGAAGAAGGACACC[C/T]GTTAGCAAGCAGAGG | 9870 |
rs756350230 | in-del | -/A/AA | | | intron-variant, splice-acceptor-variant | AREL1 | GRCh38.p7 | 14:74698858 | TGAGATCCCATCTCT[-/A/AA]AAAAAAAAAAAAAAA | 9870 |
rs756372757 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668269 | AAGGGAACTTTGAAG[C/G]AGCCCTGAAGCACAG | 9870 |
rs756414440 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714698 | TCCAGGTACTGTGCT[C/T]TGCACTAGAGTTATT | 9870 |
rs756432379 | snp | C/T | 1.66391e-05 | 0.00288431 | missense | AREL1 | GRCh38.p7 | 14:74667491 | TGTTCCACCTCCTCT[C/T]TCACTTGACTGGCCA | 9870 |
rs756457334 | snp | A/G | 3.31318e-05 | 0.00406999 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676240 | GCAGGGTGAGTCGCA[A/G]GAACACCTGGAAAGT | 9870 |
rs756458756 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700819 | AGGAATGTTAAAGGA[A/C]TATGACTTCATTTTA | 9870 |
rs756478557 | snp | G/T | 0.000815062 | 0.0201709 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661350 | GACGAATCTGCAGCA[G/T]GGCTTGGTCTCTGCC | 9870 |
rs756556114 | snp | C/T | 5.14999e-05 | 0.00507418 | intron-variant | AREL1 | GRCh38.p7 | 14:74676363 | TAACATATAGTATTT[C/T]CCCATTTACAAGCCA | 9870 |
rs756616564 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705358 | TTATAGTCTATTTCT[A/G]AATTTGGAAAGATTT | 9870 |
rs756626476 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673312 | CCAACCAACAACAAT[-/AA]GTTAGGCTTGTTTTC | 9870 |
rs756641435 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706897 | CTGGAAGCAAAGTCA[A/G]CTCTTCCATAGAGTT | 9870 |
rs756665816 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697463 | TCAGACACTTTGGAT[C/T]ATCAGTTTACATTTA | 9870 |
rs756705412 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693387 | ACTAAATAAAGTCCA[A/G]TAAAGTCAGTTTATA | 9870 |
rs756708610 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672167 | ATTCAATAACAAGAA[G/T]TTTCTTCTGTAATCA | 9870 |
rs756714330 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712084 | AAAAAAAAGAAAGAA[-/AG]AGAAAGAAAGAAAAA | 9870 |
rs756757042 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672573 | AAATCCCATCTTTAC[-/A]AAAAAATACAAAAAT | 9870 |
rs756807671 | snp | C/T | 1.66258e-05 | 0.00288316 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685639 | GTCAATGCCAACAGA[C/T]AGCCGAGGATCACAG | 9870 |
rs756814480 | snp | A/G | 1.65597e-05 | 0.00287743 | intron-variant | AREL1 | GRCh38.p7 | 14:74663865 | CTCATACCACCAAAA[A/G]CACTGGGCATGCATC | 9870 |
rs756841770 | snp | C/T | 3.3123e-05 | 0.00406945 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676682 | TATTTGAAGGGTGTG[C/T]GGCTGCCCACAGGTC | 9870 |
rs756890860 | snp | A/G | 1.65685e-05 | 0.00287819 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663979 | GGCGGCAAAGCCTCC[A/G]GGTGGTAGCTGAGAG | 9870 |
rs756929556 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681366 | TTATGCTGAGTGAGG[-/AA]AAGTCAACCCCAACA | 9870 |
rs756935842 | snp | G/T | 1.68667e-05 | 0.00290397 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674087 | AGGGGATGATCTTCA[G/T]GTAGAACTCCTTCAC | 9870 |
rs756956441 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671068 | GTATTCTGATCACTA[A/C]GGAAAAGCCCCCTAG | 9870 |
rs756982970 | snp | A/G | 1.66463e-05 | 0.00288494 | intron-variant | AREL1 | GRCh38.p7 | 14:74683552 | CCATGGGGAGAAGAA[A/G]GACACCTGTTAGCAA | 9870 |
rs756991389 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697610 | CTATTGTGGTTTAGC[C/G]AAGTTACATGGTTTT | 9870 |
rs756993224 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711500 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAAC | 9870 |
rs757077383 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698752 | AAGCAGGCTGAGCAT[A/G]GTGGTTCATACCTGT | 9870 |
rs757105954 | snp | A/C | 1.65603e-05 | 0.00287747 | stop-gained, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683431 | GCTCCTGAAGGACTT[A/C]CTGGGTCACTGGAAT | 9870 |
rs757129791 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684335 | AGTAGCAATTCACTA[A/G]TTCCTGGAGGGAGTT | 9870 |
rs757157348 | snp | A/G | 1.65809e-05 | 0.00287926 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667376 | GACCAATTCATTCAG[A/G]CCTGAAACAAAGTAG | 9870 |
rs757210119 | snp | A/G | 1.66674e-05 | 0.00288676 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675706 | GGTCCAACCTTTGGT[A/G]ACACATAGCAGTACA | 9870 |
rs757279794 | snp | C/G | 1.67536e-05 | 0.00289423 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713094 | TTGCCCTTTCCCCAA[C/G]GAGTTTCCGCTTCCG | 9870 |
rs757337189 | snp | G/T | 1.65658e-05 | 0.00287795 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676234 | GAGAATGCAGGGTGA[G/T]TCGCAAGAACACCTG | 9870 |
rs757373688 | in-del | -/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663130 | GACACCACAAAAAAA[-/T]ATTCTTTTTAGCAGT | 9870 |
rs757405845 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708703 | TAACAAGCTGCACTG[-/AA]ATAAATGCCTTCGCT | 9870 |
rs757436748 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691438 | TAGTGAAGTATTTGG[A/G]GAAAAAAAGATTTAT | 9870 |
rs757442593 | snp | A/G | 1.64738e-05 | 0.00286995 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713148 | ATGTGAATGACGTAG[A/G]AGTATTGCGCCGTTG | 9870 |
rs757574280 | snp | C/T | 0.000186759 | 0.0096615 | intron-variant | AREL1 | GRCh38.p7 | 14:74672040 | GGAATGTAAGAACTA[C/T]GCCAGTGTCTGTGCA | 9870 |
rs757574603 | snp | C/T | 1.68108e-05 | 0.00289916 | intron-variant | AREL1 | GRCh38.p7 | 14:74664974 | TCAGAGAGACAAAGA[C/T]CCAATATAAGGTCAA | 9870 |
rs757583463 | snp | A/G | 4.97748e-05 | 0.00498848 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669769 | TGGGTCATCTGTTTC[A/G]AAGTACTGAGGAGGC | 9870 |
rs757606025 | snp | C/G | 1.66084e-05 | 0.00288165 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684615 | GGAAGCTGACTACAC[C/G]TGCGGCAAGCTCAAA | 9870 |
rs757618989 | snp | C/G | 1.65619e-05 | 0.00287762 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714858 | TTGGATTTAATTTAC[C/G]TTTTTCTTCCTAGTA | 9870 |
rs757620943 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669187 | GGCCATGAGCCACTG[C/G]GCCCAGCCAAAAAGT | 9870 |
rs757628246 | snp | A/C | 1.67739e-05 | 0.00289597 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669624 | TGGAGAACATAGGAC[A/C]CAGAGGCTTTGTCCT | 9870 |
rs757670865 | snp | C/T | 1.78768e-05 | 0.00298966 | intron-variant | AREL1 | GRCh38.p7 | 14:74684706 | GAGAGAACACACAAA[C/T]CGCCTGCCAGTTACA | 9870 |
rs757706237 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673229 | GAAAACTGGTAAAGA[A/C]AAACAAAGAAATTAA | 9870 |
rs757763472 | snp | A/G | 1.70203e-05 | 0.00291716 | intron-variant | AREL1 | GRCh38.p7 | 14:74676103 | GGCAAAGAAACGGCT[A/G]AAGAACAGCACTAAA | 9870 |
rs757822712 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680961 | GCCAAGGCAGGAGGA[C/T]TGCTTGAGGCCAGGA | 9870 |
rs757888981 | snp | C/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661132 | TCCAGGTGTACACTC[C/T]ACCCCGAGCCGACCA | 9870 |
rs757924011 | snp | C/G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707081 | ATCAAAATTATACAC[C/G/T]ATCTGGTCGGGCACA | 9870 |
rs757926059 | snp | A/G | 1.66394e-05 | 0.00288434 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670000 | AAGAGCGGGTGAAGC[A/G]AGCTCGGACCAACTG | 9870 |
rs757955274 | snp | A/G | 1.66219e-05 | 0.00288283 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685627 | ACATCAGGTCCCGTC[A/G]ATGCCAACAGACAGC | 9870 |
rs757996581 | snp | C/T | 0.000286005 | 0.0119549 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674068 | CGGAAGGTGTAAAGG[C/T]GCCAGGGGATGATCT | 9870 |
rs758116485 | snp | A/T | 3.33444e-05 | 0.00408303 | intron-variant | AREL1 | GRCh38.p7 | 14:74664957 | AGGTGTTACTATGAC[A/T]GTCAGAGAGACAAAG | 9870 |
rs758143815 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710743 | TTTCTACATCAAAAA[G/T]TCAGTGCCCACAGAT | 9870 |
rs758145526 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700575 | CGAGTTCAGGAGATC[A/G]AGACCATTCTGGCTA | 9870 |
rs758150427 | snp | A/T | 1.64741e-05 | 0.00286998 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713142 | AGCAGTATGTGAATG[A/T]CGTAGAAGTATTGCG | 9870 |
rs758152916 | snp | A/G | 3.31192e-05 | 0.00406921 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663750 | GCCCTCGCAACCCTC[A/G]CTGATGGCCAGCTGC | 9870 |
rs758167846 | snp | A/G | 3.50478e-05 | 0.00418601 | intron-variant | AREL1 | GRCh38.p7 | 14:74671368 | AGGTGCGAGTGGGGA[A/G]GAGAGTTCAAAAAGA | 9870 |
rs758191867 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705553 | TTGAAGTTAAGCCAG[A/G]GACAATAAACTAGTT | 9870 |
rs758203356 | snp | G/T | 1.72136e-05 | 0.00293369 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713085 | CTCGGGGGATTGCCC[G/T]TTCCCCAAGGAGTTT | 9870 |
rs758249460 | snp | C/T | 3.39432e-05 | 0.00411952 | intron-variant | AREL1 | GRCh38.p7 | 14:74673263 | ATAAAACCCTCAAGG[C/T]CAGTAAAAGTCCTCC | 9870 |
rs758256015 | snp | C/T | 1.65734e-05 | 0.00287862 | missense | AREL1 | GRCh38.p7 | 14:74664849 | ACCTTTTCTCTGAAA[C/T]GCCATGAGCCACCAA | 9870 |
rs758324094 | in-del | -/AAA | 0.5 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74698859 | TGAGATCCCATCTCT[-/AAA]AAAAAAAAAAAAAAA | 9870 |
rs758334009 | snp | A/T | 1.65603e-05 | 0.00287747 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683418 | ACGTTGGAATTGGGC[A/T]CCTGAAGGACTTCCT | 9870 |
rs758339975 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678099 | TTAGTTAAGATTATT[A/C]TAAAATTTAAATGGA | 9870 |
rs758486583 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690245 | ACTCCAACTGCACAA[C/T]AGAGCAAGACCCTGT | 9870 |
rs758612265 | snp | C/G | 4.99613e-05 | 0.00499781 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675883 | GCATTATAAAGATAA[C/G]CCTCAAAGTAAATGC | 9870 |
rs758672204 | snp | A/G | 1.66175e-05 | 0.00288244 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670848 | GCTCAAACCATTCCC[A/G]GCGAGGCCCTCCCCA | 9870 |
rs758694659 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691601 | CAAAGAAAAGTGGAA[A/T]GCAATGCCAATTCTC | 9870 |
rs758705729 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703526 | TAAGTTTGGAGTGTC[C/T]ACAGGATATCCAGGT | 9870 |
rs758705914 | snp | C/T | 1.65875e-05 | 0.00287984 | intron-variant | AREL1 | GRCh38.p7 | 14:74673073 | AATCCCTGTGTAACC[C/T]CACCTATGTTCTTAT | 9870 |
rs758705986 | snp | A/G | 1.6649e-05 | 0.00288518 | missense | AREL1 | GRCh38.p7 | 14:74667510 | CTTGACTGGCCAGCC[A/G]ATATTGGGCCAGCAA | 9870 |
rs758720467 | snp | C/T | 1.65647e-05 | 0.00287786 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676217 | AGCATGGAAGCAGCC[C/T]CGAGAATGCAGGGTG | 9870 |
rs758749485 | snp | G/T | 1.66679e-05 | 0.00288681 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713529 | GACCATGAAGCGAAT[G/T]CTTAGTCTCAGAGAT | 9870 |
rs758807415 | snp | C/G/T | 0.000334834 | 0.0129354 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714836 | TTGCTGTGGTTTTTC[C/G/T]TCTCCCTTGGATTTA | 9870 |
rs758829441 | snp | A/G | 9.93674e-05 | 0.00704796 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672902 | TCATATGTACCTGCC[A/G]AAGCTCTCGCTGGAA | 9870 |
rs758866425 | snp | A/C/T | 5.79983e-05 | 0.00538483 | intron-variant | AREL1 | GRCh38.p7 | 14:74676793 | CATTTATTTATTTTA[A/C/T]TTTTTTATTTTTATT | 9870 |
rs758986950 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710960 | GCTGGTGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 9870 |
rs759009634 | in-del | -/ACCTACCGATTCC | 1.65741e-05 | 0.00287868 | intron-variant | AREL1 | GRCh38.p7 | 14:74672825 | CAGAGATGAAATTTT[-/ACCTACCGATTCC]AACAAGGCATGTCTG | 9870 |
rs759019025 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709993 | TTCTCTTCAAGACTG[A/C]AGAAAAATGCAAAAC | 9870 |
rs759021376 | snp | A/G | 5.08229e-05 | 0.00504072 | intron-variant | AREL1 | GRCh38.p7 | 14:74671500 | TGAAAAGAAGTGAAA[A/G]GAAGGGAATTGTCAG | 9870 |
rs759045104 | snp | C/T | 1.66087e-05 | 0.00288168 | missense | AREL1 | GRCh38.p7 | 14:74667335 | TCAAGCTCATTCTCA[C/T]CAAAAATAGCCAAAA | 9870 |
rs759077117 | snp | C/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712775 | CTGGACCATAGACAC[C/G]GGATACCCCAACGCT | 9870 |
rs759096480 | in-del | -/ACAC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704563 | TCTGAACAGAATGAG[-/ACAC]AGATTTGCCCTAAGC | 9870 |
rs759098450 | snp | C/T | 3.33122e-05 | 0.00408105 | intron-variant | AREL1 | GRCh38.p7 | 14:74664951 | ATGGTAAGGTGTTAC[C/T]ATGACAGTCAGAGAG | 9870 |
rs759128259 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680601 | TAAGTGAATATTTAT[A/C]GCAGCTTTATTCATC | 9870 |
rs759214091 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692440 | GAAACCCTGGGACAC[C/T]AAAAATAACCAAAAA | 9870 |
rs759242955 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702735 | GCTGCAAATTTTCCA[A/G]ACTTTTATGCTCTGC | 9870 |
rs759256664 | snp | C/T | 1.65899e-05 | 0.00288005 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683518 | CAGGGAAAGGCTGCC[C/T]GTTCTTATAGAATAA | 9870 |
rs759257348 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688649 | ATCAATTCATCATTC[A/G]CTGACATCAACTTTA | 9870 |
rs759265509 | in-del | -/AACCT | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662543 | CATCATTCAACAGTG[-/AACCT]AACCTAATAAGCTTC | 9870 |
rs759318078 | snp | C/T | 3.31296e-05 | 0.00406985 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676198 | GATTTTGGTATGAAA[C/T]GCAAGCATGGAAGCA | 9870 |
rs759342707 | snp | A/G | 1.65641e-05 | 0.00287781 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663690 | GAAGCTCCAGAGAGC[A/G]TGGGAGCCAACTGGA | 9870 |
rs759429926 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703706 | TAGTACTCCATTAAA[C/T]GGACATACTGCAATC | 9870 |
rs759466905 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668918 | GGTTTTGCTGTGTCA[C/T]CCAGGCTGGAGTGCA | 9870 |
rs759470857 | snp | A/G | 1.67472e-05 | 0.00289367 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684659 | GTGAAGAAGAATGCA[A/G]CCACAGACACTGTGA | 9870 |
rs759474118 | in-del | -/AGA | 1.66832e-05 | 0.00288814 | cds-indel | AREL1 | GRCh38.p7 | 14:74667534 | CCAGCAAATTTAAAT[-/AGA]AGATTTTATTCGCAT | 9870 |
rs759495637 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671556 | TTAAAGACAACACAA[C/G]AGCACTGCCATTGTC | 9870 |
rs759589699 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665496 | TCCTGACAGTCTGCT[C/T]TAAACTTAGCCTGGG | 9870 |
rs759611274 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695737 | AATAGATTGCGGACT[C/T]CCCAAGGAACACTGA | 9870 |
rs759613104 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682121 | ATTCATATGAAAAGG[A/C]GTATCTGAGTGAGGC | 9870 |
rs759656178 | snp | A/G | 3.31565e-05 | 0.0040715 | intron-variant | AREL1 | GRCh38.p7 | 14:74673038 | CATGGATGTGGCTGG[A/G]CTCACTACCTTCCCT | 9870 |
rs759656193 | snp | A/G | 3.5097e-05 | 0.00418894 | intron-variant | AREL1 | GRCh38.p7 | 14:74683262 | AGAGAGAGGGAAGGA[A/G]ACAAAGGGAAAAAGA | 9870 |
rs759660504 | in-del | -/AAAAT | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711548 | CTCTGTCTCAAAAAT[-/AAAAT]AAAATAAAATAAAAT | 9870 |
rs759682514 | snp | C/G | 1.65663e-05 | 0.002878 | missense, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669696 | CTTCTGCAAAGACCA[C/G]CTCCATCTCACTCAT | 9870 |
rs759716012 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714550 | CTGTCACCCTTTTAC[C/T]CATTGCTTGGAAGTG | 9870 |
rs759728664 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707461 | AGGTCAGGAGATCGA[A/G]ACCACCCTGGCTAAA | 9870 |
rs759754971 | snp | A/G | 1.72403e-05 | 0.00293596 | intron-variant | AREL1 | GRCh38.p7 | 14:74669927 | GGGCCTTAGTAGGAA[A/G]TGCACACCCAAGATG | 9870 |
rs759788465 | snp | A/C | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661215 | CCCCACCTTCCAGTC[A/C]AGCCATGAATCTCCA | 9870 |
rs759963565 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706772 | ACAAATAAATAATTA[C/T]GTAGTTATACTTCCG | 9870 |
rs759974019 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663964 | AAATGAGGGACAGAG[A/G]GCGGCAAAGCCTCCA | 9870 |
rs760029346 | snp | A/G | 7.08378e-05 | 0.00595096 | intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670140 | ACCTGTCCAAGAAAG[A/G]GACTGAAAGGCCCTG | 9870 |
rs760049840 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662293 | AGGCCAAGGCATTGC[C/T]AAAGTCCTGCCTTGT | 9870 |
rs760082642 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712038 | TGGAAGACAAAGTGC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 9870 |
rs760114364 | snp | C/G | 2.34623e-05 | 0.003425 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713057 | GTTGGTCTCCACCCG[C/G]CCTGGGAACCGGCTC | 9870 |
rs760115895 | snp | C/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712847 | CCAGGAGTCTGAACC[C/G]CCCTACCCTTTTCCT | 9870 |
rs760133498 | snp | C/G | 6.42791e-05 | 0.00566881 | intron-variant | AREL1 | GRCh38.p7 | 14:74664085 | ATGACCTGGCAGGGA[C/G]AGCACAAGGCTGGGA | 9870 |
rs760152663 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662208 | TGAGGTCAGGCAGGA[A/C]CTGTAGCAGCTCAGG | 9870 |
rs760160335 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667296 | CCAAGTTAAGAATGG[C/G]AGTCTGAATTGCAAT | 9870 |
rs760161331 | snp | A/C/T | 0.000223119 | 0.01056 | intron-variant | AREL1 | GRCh38.p7 | 14:74671358 | TTTGTGGAGAAGGTG[A/C/T]GAGTGGGGAGGAGAG | 9870 |
rs760169529 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698405 | CCAAATCTGGGAGGC[A/G]TGAAATGGGGTTACA | 9870 |
rs760197143 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663608 | ACACAGGGGAGCATG[C/T]GGCATCTTCTGGCTG | 9870 |
rs760214212 | snp | G/T | 1.65817e-05 | 0.00287933 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670816 | ATTGGTGGTATCAAA[G/T]AGTGCTTTGCAGATT | 9870 |
rs760216411 | snp | G/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676177 | ATTCACCATTATTGA[G/T]TGGCTGATTTTGGTA | 9870 |
rs760219444 | snp | C/G/T | 0.00397167 | 0.0443867 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713073 | CCTGGGAACCGGCTC[C/G/T]GGGGATTGCCCTTTC | 9870 |
rs760221707 | in-del | -/C | 1.67961e-05 | 0.00289789 | frameshift-variant, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670088 | AAACTCATACATTTT[-/C]AGGCGCAGATGAGCG | 9870 |
rs760324944 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678133 | GCAAAGGAACTAGAA[C/T]ACTAAAACAATTTTG | 9870 |
rs760376838 | snp | A/G | 1.70336e-05 | 0.00291831 | intron-variant | AREL1 | GRCh38.p7 | 14:74683279 | CAAAGGGAAAAAGAA[A/G]GGAAAAAAGAACCTA | 9870 |
rs760379024 | snp | A/G | 1.64776e-05 | 0.00287028 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713127 | CTATCCTTTGCCGGA[A/G]GCAGTATGTGAATGA | 9870 |
rs760380035 | snp | G/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711391 | TAAAAATACAAAAAT[G/T]AGCAAGGTATGGTGG | 9870 |
rs760449857 | snp | A/G | 1.65842e-05 | 0.00287955 | stop-gained, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684576 | TAGTCCGGTCCCCTC[A/G]GCGCTCGCGGTCCTC | 9870 |
rs760464486 | in-del | -/CCT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701645 | CATTCCACCCCGGCC[-/CCT]CCTCCCAAATCTCAT | 9870 |
rs760476046 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688950 | CAAGCAATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 9870 |
rs760519072 | snp | C/G | 1.65671e-05 | 0.00287807 | synonymous-codon, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669691 | TTTCTCTTCTGCAAA[C/G]ACCAGCTCCATCTCA | 9870 |
rs760530193 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691244 | AAGACTGCTTGAGCC[C/T]AGGAGGTCAAGGCTG | 9870 |
rs760551209 | snp | A/G | 1.6701e-05 | 0.00288968 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684652 | CTTAATTGTGAAGAA[A/G]AATGCAACCACAGAC | 9870 |
rs760570392 | snp | C/T | 1.66065e-05 | 0.00288149 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673164 | GAGGTTGAATGCCAT[C/T]ATCCACCACCAGTGT | 9870 |
rs760586838 | snp | A/C | 1.68391e-05 | 0.0029016 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713592 | AGGGATATTCTAATA[A/C]GAGTCTAGAGAGGAT | 9870 |
rs760599667 | snp | C/G | 1.76005e-05 | 0.00296647 | intron-variant | AREL1 | GRCh38.p7 | 14:74667628 | GACAGACAAGGGAGA[C/G]GCTGTGGATGGAAAT | 9870 |
rs760627224 | snp | C/T | 1.76493e-05 | 0.00297058 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675945 | GATATTCTTCTCATC[C/T]TCTGAAGTATAATAA | 9870 |
rs760688454 | snp | C/T | 6.63207e-05 | 0.00575812 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676745 | GGTCTTAGAAGGAAC[C/T]ACCATTCCTGGAACA | 9870 |
rs760732861 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692317 | TCGACTGCCAAAGGA[C/T]GCCCCAGGATCCTGT | 9870 |
rs760739444 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683082 | TGACTACTAACATGT[A/G]TGGGGTTTCTTTTTG | 9870 |
rs760747453 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672888 | GGAATGTGGTCTTTT[C/T]ATATGTACCTGCCGA | 9870 |
rs760747842 | in-del | -/AAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678696 | AAGACATGTATAAGC[-/AAA]AAAAAAAAAAAAAAA | 9870 |
rs760748517 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703888 | CATATGGTAAGTATC[G/T]ACTTAACTTACAAGA | 9870 |
rs760774820 | snp | A/G | 3.37001e-05 | 0.00410474 | upstream-variant-2KB, utr-variant-5-prime, missense | AREL1, FCF1 | GRCh38.p7 | 14:74713495 | TCAAGGGGAAGCAAA[A/G]GAAAACAAGGAAGTA | 9870 |
rs760810949 | snp | A/G | 0.000124185 | 0.0078789 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712985 | CGCTGTCCTGGGAAG[A/G]GGCGGCAGCACTCAG | 9870 |
rs760842003 | snp | C/G | 1.65712e-05 | 0.00287843 | intron-variant | AREL1 | GRCh38.p7 | 14:74672983 | ATCCATCATTACAGC[C/G]TCATTACAAGCCATC | 9870 |
rs760848457 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697033 | CCCCTGTTGTCCTAG[C/G]TACTCAGAAGCTAAG | 9870 |
rs760873316 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702930 | CCTCAGCCTGGATTT[C/T]AATGTCCATATCATC | 9870 |
rs760874049 | snp | A/C | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676648 | TGTTGGTGGGATTAT[A/C]ATACTCATCTCGGGG | 9870 |
rs760881491 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708673 | AACAGATGTTAACTA[C/T]TGGCATCTCAACAGT | 9870 |
rs760969205 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709350 | TGGTACTAATATGTT[C/G]ATAGTATTAAATAAA | 9870 |
rs761034413 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707552 | TGTAATCCCAGCACT[C/T]TGGGAGGCCCAGGCA | 9870 |
rs761037003 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673966 | GTGCTTCTGAGAAAA[A/G]ATAAAAGGCTGAGAT | 9870 |
rs761071199 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674987 | AAAATTTTTTAATCT[C/T]AAAAAATCCCTTTTA | 9870 |
rs761088391 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661488 | CACAAGGACATAAAT[A/C]AAAGAACTGGCCAAA | 9870 |
rs761111127 | snp | A/C | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675770 | GGCACTCAGAGGGCG[A/C]GTCTTCATCTTCCTC | 9870 |
rs761126156 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695861 | TGTATGCTGAAGTTT[G/T]AGAAACATGGTTTAG | 9870 |
rs761148217 | snp | C/T | 0.000213789 | 0.0103368 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692303 | AGTGCAGGGTGCAAT[C/T]GACTGCCAAAGGACG | 9870 |
rs761164346 | snp | A/G | 3.45346e-05 | 0.00415525 | intron-variant | AREL1 | GRCh38.p7 | 14:74675661 | ATTACACACAGGTTC[A/G]AGCAGGGGGATTTTA | 9870 |
rs761182486 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662583 | TAGTTCTCCTTCCTG[A/G]TAACTGATGGAGCAA | 9870 |
rs761252398 | snp | C/G | 0.000121675 | 0.00779888 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675930 | CACATTGCGTTCGAC[C/G]ATATTCTTCTCATCC | 9870 |
rs761371592 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686363 | TCACTGTTGTTAAAC[G/T]TGTTTCCAGAATAAG | 9870 |
rs761377307 | snp | C/T | 1.65811e-05 | 0.00287929 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684566 | TAGTCATAAATAGTC[C/T]GGTCCCCTCGGCGCT | 9870 |
rs761377462 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675813 | GGATGGCCGGCGCTG[A/G]GAAGAGGTCATGTGC | 9870 |
rs761434673 | snp | C/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712881 | TCTCTCTCTGGAACT[C/G]TGGTAAAGGCAGGTC | 9870 |
rs761463028 | in-del | -/A | 0.000734664 | 0.0191518 | intron-variant | AREL1 | GRCh38.p7 | 14:74671370 | GTGCGAGTGGGGAGG[-/A]GAGTTCAAAAAGATG | 9870 |
rs761498877 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693741 | CTGCTTTTAATGACT[A/C]CTCTACTGCCTCTCC | 9870 |
rs761504016 | snp | G/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714225 | TTGGGAGGCTGAGGC[G/T]GGTGGATCACCTGAG | 9870 |
rs761504188 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700271 | AGCATACTTTATCCA[C/T]ATTTTATAGATTAGG | 9870 |
rs761506805 | snp | A/G | 3.26376e-05 | 0.00403952 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713033 | ACTCTCCCACCAACA[A/G]ACCCCAGAGTTGGTC | 9870 |
rs761519601 | snp | A/G | | | missense | AREL1 | GRCh38.p7 | 14:74667554 | ATTTTATTCGCATTG[A/G]TGACTGGAGTTTGAG | 9870 |
rs761529429 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665979 | GCTTTGCTTCAAAAT[A/G]TAACAAAATTTACCA | 9870 |
rs761566615 | in-del | -/GG | 1.76799e-05 | 0.00297315 | intron-variant | AREL1 | GRCh38.p7 | 14:74683253 | ATGGAAAGAGAGAGA[-/GG]GGGAAGGAGACAAAG | 9870 |
rs761574617 | snp | A/C | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713212 | CATGGTGAGAGAAGA[A/C]GGTCCAAGAAGGGAC | 9870 |
rs761625046 | snp | A/C | 1.77476e-05 | 0.00297884 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713466 | CCAACTTTTTTAATT[A/C]TAAAATTTCTGTTTC | 9870 |
rs761627875 | snp | A/G | 1.67033e-05 | 0.00288987 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713559 | TCAGAGGCTGTGAGT[A/G]TCTGGAATCAACTGC | 9870 |
rs761683254 | snp | A/T | 1.65677e-05 | 0.00287812 | intron-variant | AREL1 | GRCh38.p7 | 14:74672973 | GAACAGCAAGATCCA[A/T]CATTACAGCCTCATT | 9870 |
rs761685459 | snp | A/C | 0.000150244 | 0.008666 | missense | AREL1 | GRCh38.p7 | 14:74667482 | TTTAGGAAATGTTCC[A/C]CCTCCTCTTTCACTT | 9870 |
rs761697592 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678787 | ACACATTTTCAAACT[A/G]TAAAAACTTTTGGGA | 9870 |
rs761712736 | snp | A/G | 4.9802e-05 | 0.00498984 | stop-gained, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684462 | CCCTTACATGCACTC[A/G]GAAGGCCATGCTGTG | 9870 |
rs761729718 | snp | C/T | 0.0019674 | 0.0313022 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692194 | TCCATCAGACTTTGT[C/T]ACAGTAATCAGGTCA | 9870 |
rs761734099 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703927 | AACCGTTTACCAAAG[C/T]GGCTGGACCACTTTG | 9870 |
rs761740408 | snp | C/G | 6.62427e-05 | 0.00575473 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672874 | TTCAGGGTGACTTTG[C/G]AATGTGGTCTTTTCA | 9870 |
rs761768548 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671586 | CTGCTGGACTAACTA[C/T]GACTGCCTGAAGGAG | 9870 |
rs761850036 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692718 | TGTTTTTGTTTTTGT[C/T]TTTGAGACAGGGTCT | 9870 |
rs761880187 | snp | C/T | 1.65594e-05 | 0.0028774 | missense | AREL1 | GRCh38.p7 | 14:74663800 | CATAGGAGTCATATG[C/T]AGGGAGGCACAGCTG | 9870 |
rs761882715 | snp | A/G | 1.67336e-05 | 0.00289249 | intron-variant | AREL1 | GRCh38.p7 | 14:74676327 | GAGGGCCGAGCTATA[A/G]GAAGGCAACAGAGCA | 9870 |
rs761933020 | snp | C/T | 1.65605e-05 | 0.0028775 | stop-lost | AREL1 | GRCh38.p7 | 14:74663720 | ATGACAGGAGAGTGG[C/T]CAGAGCATGCCAAAG | 9870 |
rs761958910 | snp | C/T | 1.65704e-05 | 0.00287836 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676612 | AGGTGTAATTGTGCT[C/T]ATCTCTCAAGGACAT | 9870 |
rs761962522 | snp | C/T | | | intron-variant, utr-variant-5-prime | AREL1 | GRCh38.p7 | 14:74698819 | GCTTGCGCCCAGGAG[C/T]TCAAGACCAATCTGG | 9870 |
rs761996251 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666229 | AAGAAAACCTTCCTC[C/T]CTAAAGAAACGTTTG | 9870 |
rs761997282 | snp | A/C/T | 3.32365e-05 | 0.00407644 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670056 | TCATAGAGACACTTG[A/C/T]CCACGAGCCGTCCCG | 9870 |
rs762022087 | snp | G/T | 1.72779e-05 | 0.00293916 | intron-variant | AREL1 | GRCh38.p7 | 14:74674023 | TGAACCAGATGTAAG[G/T]TTCAGCTTACTTTTG | 9870 |
rs762039755 | snp | A/G | 1.65583e-05 | 0.00287731 | missense | AREL1 | GRCh38.p7 | 14:74663920 | TGTGCAGTAGGCAGC[A/G]TGCTATGGGTCGGAG | 9870 |
rs762048025 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670116 | GCGGGGCGATTAGGG[C/T]TGGGATGCACCTGTC | 9870 |
rs762187508 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662670 | TCCCTAGTGTCCTGA[C/T]GCCAAGGACCTGTGA | 9870 |
rs762217236 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663311 | GGTCAAGTAGTGAGG[A/G]CCAAAGAGGGTGTCT | 9870 |
rs762243702 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683187 | AGGATGAATTTTATG[C/G]CATGGGAATTAAATC | 9870 |
rs762255128 | snp | A/G | 3.37291e-05 | 0.00410651 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669969 | TGCATACGCAGTCCT[A/G]TGATTTGGGCCAGGA | 9870 |
rs762333583 | snp | A/C | 1.65605e-05 | 0.0028775 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683382 | CGCCCAGCCTTGCGC[A/C]CAGTGAAGGCCACTT | 9870 |
rs762418819 | snp | A/C | 1.65987e-05 | 0.00288082 | intron-variant | AREL1 | GRCh38.p7 | 14:74667455 | AGGCCAAGAACAGAC[A/C]GGATCCCACCTTTTA | 9870 |
rs762441110 | snp | C/T | 1.6609e-05 | 0.0028817 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683531 | CCCGTTCTTATAGAA[C/T]AACTGCCATGGGGAG | 9870 |
rs762448622 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688493 | TACTGATTTTCAAGA[C/T]CAGCTAAACCTTCTC | 9870 |
rs762458035 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709474 | CAGCCACCAACCATA[C/T]TTTACCTATTTACAA | 9870 |
rs762465037 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675369 | AGAAACTAACACAAA[C/G]TGCTTCTTAGCTCAG | 9870 |
rs762471013 | snp | A/G | 1.66125e-05 | 0.00288201 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684454 | GAAACATTCCCTTAC[A/G]TGCACTCGGAAGGCC | 9870 |
rs762608064 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665793 | TCATCCAATAGCTAT[A/G]AAGAATAATACATTC | 9870 |
rs762620870 | in-del | -/TG | 1.66949e-05 | 0.00288915 | upstream-variant-2KB, splice-donor-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713552 | TCAGAGATCAGAGGC[-/TG]TGAGTGTCTGGAATC | 9870 |
rs762644132 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687648 | CTTTGTAAAGGAGTG[C/T]CAGTTTCCTTATATG | 9870 |
rs762677977 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701599 | ACTATAATTCAAGAT[A/G]AGATTTGGATGGGGA | 9870 |
rs762699515 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675788 | CTTCATCTTCCTCGT[C/T]AACAGCAGTGGATGG | 9870 |
rs762797738 | snp | G/T | 5.23638e-05 | 0.00511656 | intron-variant | AREL1 | GRCh38.p7 | 14:74671528 | CAGAACACTGGCTGG[G/T]GTCCTCTGGATGTTA | 9870 |
rs762814265 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667771 | TAGTTCCTAAGCTTC[A/C]GGGTTCCTACCACTA | 9870 |
rs762845721 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692291 | GACTTCTCTCTAGTG[-/C]CAGGGTGCAATCGAC | 9870 |
rs762885076 | snp | C/T | 1.67153e-05 | 0.00289091 | splice-acceptor-variant | AREL1 | GRCh38.p7 | 14:74676323 | TCTTGAGGGCCGAGC[C/T]ATAGGAAGGCAACAG | 9870 |
rs762935905 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692837 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGCGTGC | 9870 |
rs763006454 | snp | A/G | 1.71387e-05 | 0.00292729 | splice-donor-variant, intron-variant | AREL1 | GRCh38.p7 | 14:74669945 | CACACCCAAGATGTT[A/G]CCTTGTAATGCATAC | 9870 |
rs763012599 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706680 | CATGCCAAGCAATAT[G/T]TTGGACCCTAAAGAT | 9870 |
rs763048750 | snp | C/G | 0.000546471 | 0.0165208 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672848 | ATTCCAACAAGGCAT[C/G]TCTGCTGACCTTCAG | 9870 |
rs763059665 | snp | G/T | 1.65679e-05 | 0.00287814 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669724 | CATGTCATTGTTGAG[G/T]ATAAAACAAACTTTA | 9870 |
rs763104571 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694005 | GACATAACAAAACCC[C/T]GTCTCTACAAAAAAT | 9870 |
rs763115156 | snp | C/T | 1.65597e-05 | 0.00287743 | missense | AREL1 | GRCh38.p7 | 14:74663793 | ACCTCTTCATAGGAG[C/T]CATATGTAGGGAGGC | 9870 |
rs763149555 | snp | A/G | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661156 | CCGACCACTTCAGGA[A/G]GAATTCCTGGGGAAA | 9870 |
rs763168136 | snp | A/G | 1.65627e-05 | 0.00287769 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663703 | GCATGGGAGCCAACT[A/G]GATGACAGGAGAGTG | 9870 |
rs763173274 | snp | A/G | 1.73006e-05 | 0.00294109 | intron-variant | AREL1 | GRCh38.p7 | 14:74683271 | GAAGGAGACAAAGGG[A/G]AAAAGAAAGGAAAAA | 9870 |
rs763211090 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705143 | CTTCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCGG | 9870 |
rs763220033 | snp | A/C | 3.31664e-05 | 0.00407211 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664920 | TCCAGTCCCACACAT[A/C]AGCAGCTGGAAAAAG | 9870 |
rs763255486 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693056 | CTTCAGCACAACCAC[A/G]TACCCAGTTTGAATA | 9870 |
rs763273036 | snp | A/G | 1.72053e-05 | 0.00293298 | intron-variant | AREL1 | GRCh38.p7 | 14:74670879 | GTCCAGAGCTGAAAA[A/G]CATAATGAAAATAAA | 9870 |
rs763294687 | snp | C/G | 1.66554e-05 | 0.00288573 | intron-variant | AREL1 | GRCh38.p7 | 14:74685580 | AAAATATAATAGAGA[C/G]AGCTCTTTCCATAAC | 9870 |
rs763339168 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708715 | CTGAAATAAATGCCT[A/T]CGCTCTGAAAAACAT | 9870 |
rs763393145 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699814 | AGTTGCCTCATATGT[A/G]AAATGGAGATGCACT | 9870 |
rs763402889 | snp | C/G | 1.66172e-05 | 0.00288242 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673200 | GCTTATGGACAGGGT[C/G]AGGACCAAGGTATGA | 9870 |
rs763408152 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684776 | CAAAAATTAAAGGAG[A/G]TCAGGATGAGACTGT | 9870 |
rs763425085 | snp | C/T | 2.37617e-05 | 0.00344678 | intron-variant | AREL1 | GRCh38.p7 | 14:74664102 | GCACAAGGCTGGGAT[C/T]ACACACAGTAAACAA | 9870 |
rs763428431 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686074 | GGGAGTAATTCAGCT[A/C]AGTAGAAATAGCTAT | 9870 |
rs763464411 | snp | C/T | 4.96824e-05 | 0.00498385 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675808 | GCAGTGGATGGCCGG[C/T]GCTGGGAAGAGGTCA | 9870 |
rs763481797 | snp | A/G | 2.1488e-05 | 0.00327774 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713064 | TCCACCCGGCCTGGG[A/G]ACCGGCTCGGGGGAT | 9870 |
rs763534821 | in-del | -/GTCATAAATAGTCCGGC | 1.6577e-05 | 0.00287893 | frameshift-variant, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684552 | ATTTCCCCGCACGTA[-/GTCATAAATAGTCCGGC]GTCATAAATAGTCCG | 9870 |
rs763535458 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683376 | TCATAACGCCCAGCC[C/T]TGCGCACAGTGAAGG | 9870 |
rs763601239 | snp | A/C | 3.3206e-05 | 0.00407455 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684459 | ATTCCCTTACATGCA[A/C]TCGGAAGGCCATGCT | 9870 |
rs763612853 | snp | A/G/T | 3.32874e-05 | 0.00407956 | synonymous-codon, missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670066 | ACTTGCCCACGAGCC[A/G/T]TCCCGCAAACTCATA | 9870 |
rs763622846 | snp | A/G | 1.7978e-05 | 0.00299811 | intron-variant | AREL1 | GRCh38.p7 | 14:74670150 | GAAAGAGACTGAAAG[A/G]CCCTGGGCCATTTTT | 9870 |
rs763623215 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700058 | TTCAATCTACCTGAA[A/G]GACTCACTGGTTTTC | 9870 |
rs763718929 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665893 | CTGACCAGGAACTAA[C/G]AGCAGGATGTGGAAC | 9870 |
rs763734224 | snp | G/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711473 | GCTTGAACCTGGGAG[G/T]GGGAGGTTGCTGTGA | 9870 |
rs763816610 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678354 | AGATAAAAAATTAGC[G/T]AAGCACGGTGGTGCA | 9870 |
rs763844821 | in-del | -/A | 3.39662e-05 | 0.00412092 | intron-variant | AREL1 | GRCh38.p7 | 14:74670875 | CCCAGTCCAGAGCTG[-/A]AAAGCATAATGAAAA | 9870 |
rs763901401 | snp | C/T | 4.94222e-05 | 0.00497078 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713143 | GCAGTATGTGAATGA[C/T]GTAGAAGTATTGCGC | 9870 |
rs763908423 | snp | C/T | 1.66941e-05 | 0.00288908 | intron-variant | AREL1 | GRCh38.p7 | 14:74676768 | CTGGAACAAAGACAA[C/T]GGAATCTAACATTTA | 9870 |
rs763931110 | snp | A/C | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672868 | CTGACCTTCAGGGTG[A/C]CTTTGGAATGTGGTC | 9870 |
rs763996462 | snp | C/T | 1.76275e-05 | 0.00296874 | intron-variant | AREL1 | GRCh38.p7 | 14:74671534 | ACTGGCTGGTGTCCT[C/T]TGGATGTTAAAGACA | 9870 |
rs764009912 | snp | G/T | 1.66136e-05 | 0.00288211 | splice-acceptor-variant | AREL1 | GRCh38.p7 | 14:74683535 | TTCTTATAGAATAAC[G/T]GCCATGGGGAGAAGA | 9870 |
rs764034669 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688019 | ATACTGAGTACTTAC[-/T]TTTTTTTTTTTTTTT | 9870 |
rs764061108 | snp | A/G | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713206 | CGTGACCATGGTGAG[A/G]GAAGACGGTCCAAGA | 9870 |
rs764061373 | snp | C/T | 3.32187e-05 | 0.00407532 | intron-variant | AREL1 | GRCh38.p7 | 14:74667462 | GAACAGACAGGATCC[C/T]ACCTTTTAGGAAATG | 9870 |
rs764091072 | snp | C/T | 1.65608e-05 | 0.00287752 | intron-variant | AREL1 | GRCh38.p7 | 14:74663846 | GCAAGGGAGAAGTGA[C/T]TAACTCATACCACCA | 9870 |
rs764115143 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703915 | AAGAAACTGCCAAAC[C/T]GTTTACCAAAGCGGC | 9870 |
rs764116010 | snp | C/T | 1.71584e-05 | 0.00292898 | intron-variant | AREL1 | GRCh38.p7 | 14:74684684 | CTGTGATTCCACCTA[C/T]GCAAAAGAGAGAACA | 9870 |
rs764119516 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689225 | CATTTTCTGTAAGCA[C/T]GTTCCGACCCTGTTG | 9870 |
rs764120730 | snp | A/G | 4.96841e-05 | 0.00498393 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663707 | GGGAGCCAACTGGAT[A/G]ACAGGAGAGTGGTCA | 9870 |
rs764137903 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691246 | GACTGCTTGAGCCTA[A/G]GAGGTCAAGGCTGCA | 9870 |
rs764170036 | snp | C/T | 1.70635e-05 | 0.00292087 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669954 | GATGTTACCTTGTAA[C/T]GCATACGCAGTCCTA | 9870 |
rs764189809 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682309 | ACCCAGGGACCCCAG[A/G]TCCTATTATTTCTGT | 9870 |
rs764310654 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662606 | TGGAGCAAAGGGGAG[C/T]ACAGGGGTTGGCAGG | 9870 |
rs764311606 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703064 | GTTACCCAGTTCCAA[A/G]GTTACTTCCATATTT | 9870 |
rs764326878 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695892 | ACTCTAGAGCAATCA[A/G]TATGAGAAGGGGCTC | 9870 |
rs764356752 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697040 | TGTCCTAGCTACTCA[A/G]AAGCTAAGGCAGGAG | 9870 |
rs764357773 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669133 | CTCCTGGTCTCAAGC[C/T]ATCCTCCTGCCTCAG | 9870 |
rs764426755 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677090 | AGGCGTGAGCCACCA[C/T]GCCCGGCTGGAATCT | 9870 |
rs764430326 | snp | C/T | 3.32751e-05 | 0.00407878 | intron-variant | AREL1 | GRCh38.p7 | 14:74685592 | AGAGAGCTCTTTCCA[C/T]AACGTACCAATAACG | 9870 |
rs764434381 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683122 | AAATGCTCTAAAATC[A/G]ACTGTGATGATGGCT | 9870 |
rs764504341 | snp | C/G | 1.77546e-05 | 0.00297943 | intron-variant | AREL1 | GRCh38.p7 | 14:74674004 | AGATGAAGCATGCTT[C/G]ATGTGAACCAGATGT | 9870 |
rs764547162 | snp | A/G | 1.72065e-05 | 0.00293308 | intron-variant | AREL1 | GRCh38.p7 | 14:74683274 | GGAGACAAAGGGAAA[A/G]AGAAAGGAAAAAAGA | 9870 |
rs764580656 | snp | C/T | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669735 | TGAGGATAAAACAAA[C/T]TTTAGATTTGTAGAA | 9870 |
rs764610766 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673336 | TTGTTTTCTCCAAAT[A/G]AGGACCTACCAGAAA | 9870 |
rs764641256 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674177 | TATTTGGGTATTCTA[A/G]TTCAAATATCATAGT | 9870 |
rs764661625 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707006 | AACACTCGTCAGAGG[C/G]GATTCTTGGACCACA | 9870 |
rs764709322 | snp | G/T | 1.66454e-05 | 0.00288486 | intron-variant | AREL1 | GRCh38.p7 | 14:74673221 | CAAGGTATGAAAACT[G/T]GTAAAGAAAAACAAA | 9870 |
rs764787186 | snp | A/G | 1.6607e-05 | 0.00288153 | missense | AREL1 | GRCh38.p7 | 14:74667338 | AGCTCATTCTCATCA[A/G]AAATAGCCAAAAGGT | 9870 |
rs764804198 | in-del | -/TT | 1.65608e-05 | 0.00287752 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683358 | CAAGCTTCACTGTGA[-/TT]TTTCATAACGCCCAG | 9870 |
rs764881394 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686417 | GATCATGTGAACCAA[C/T]AAAAGTACTGCCAAG | 9870 |
rs764896385 | snp | G/T | 3.52653e-05 | 0.00419898 | intron-variant | AREL1 | GRCh38.p7 | 14:74671363 | GGAGAAGGTGCGAGT[G/T]GGGAGGAGAGTTCAA | 9870 |
rs764945793 | snp | A/G | 1.65649e-05 | 0.00287788 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676199 | ATTTTGGTATGAAAT[A/G]CAAGCATGGAAGCAG | 9870 |
rs764980029 | snp | C/T | 1.70734e-05 | 0.00292172 | intron-variant | AREL1 | GRCh38.p7 | 14:74675680 | AGGGGGATTTTATGT[C/T]GAGAATGGAAGGTCC | 9870 |
rs765007554 | snp | C/G/T | 9.93812e-05 | 0.00704853 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663691 | AAGCTCCAGAGAGCA[C/G/T]GGGAGCCAACTGGAT | 9870 |
rs765033153 | snp | C/T | 1.68952e-05 | 0.00290642 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674053 | GTTCCTGGACACACT[C/T]GGAAGGTGTAAAGGC | 9870 |
rs765059625 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680042 | TTAGCCAGGCGTGGT[A/G]GTGCCTGCCTGTAAT | 9870 |
rs765096914 | in-del | -/CCT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678972 | CACAGCTCACTGCAG[-/CCT]CAACCTCCTGGGCTT | 9870 |
rs765131440 | snp | C/T | 1.66618e-05 | 0.00288628 | intron-variant | AREL1 | GRCh38.p7 | 14:74664953 | GGTAAGGTGTTACTA[C/T]GACAGTCAGAGAGAC | 9870 |
rs765140628 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662637 | TGTTTACTGTGTAAC[A/C]TATCACCTCCATGTT | 9870 |
rs765147339 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667736 | TGTGCATTCAGCTTT[A/T]CAACACACTTGGTTT | 9870 |
rs765165149 | snp | A/G | 3.29495e-05 | 0.00405877 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713137 | CCGGAAGCAGTATGT[A/G]AATGACGTAGAAGTA | 9870 |
rs765173266 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709340 | ATCTATTACATGGTA[C/G]TAATATGTTGATAGT | 9870 |
rs765191662 | snp | A/C | 1.71684e-05 | 0.00292983 | intron-variant | AREL1 | GRCh38.p7 | 14:74671518 | AGGGAATTGTCAGAA[A/C]ACTGGCTGGTGTCCT | 9870 |
rs765262467 | snp | C/T | 3.31329e-05 | 0.00407005 | missense, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669714 | CCATCTCACTCATGT[C/T]ATTGTTGAGGATAAA | 9870 |
rs765320666 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691486 | AGTATGAGAAAACAC[C/T]ATCCAATCTTACTGT | 9870 |
rs765439001 | snp | A/G | 1.6968e-05 | 0.00291268 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713600 | TCTAATAAGAGTCTA[A/G]AGAGGATAAGTAGTA | 9870 |
rs765480574 | snp | A/G | 3.51958e-05 | 0.00419484 | intron-variant | AREL1 | GRCh38.p7 | 14:74683259 | AAGAGAGAGAGGGAA[A/G]GAGACAAAGGGAAAA | 9870 |
rs765486007 | snp | C/G | 1.80169e-05 | 0.00300135 | intron-variant | AREL1 | GRCh38.p7 | 14:74675968 | TATAATAAGGAATAA[C/G]GTTTAAAGTAGAAGT | 9870 |
rs765502562 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692724 | TGTTTTTGTTTTTGA[A/G]ACAGGGTCTTTCTCC | 9870 |
rs765510934 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704227 | CATTCTAAATGTGAA[C/T]CCCGAATATCTGAGA | 9870 |
rs765544581 | snp | C/G | 3.35677e-05 | 0.00409668 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684663 | AGAAGAATGCAACCA[C/G]AGACACTGTGATTCC | 9870 |
rs765563657 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671703 | TGATTTGCCTTTACA[A/T]CATCACTTTGTTGGA | 9870 |
rs765608575 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704977 | TCATTAAGTTTTATT[-/C]CCCTTGTTTCTTTCA | 9870 |
rs765622609 | snp | G/T | 3.31219e-05 | 0.00406938 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676677 | GGTACTATTTGAAGG[G/T]TGTGCGGCTGCCCAC | 9870 |
rs765657877 | snp | C/G | 0.000109413 | 0.00739557 | intron-variant | AREL1 | GRCh38.p7 | 14:74664088 | ACCTGGCAGGGAGAG[C/G]ACAAGGCTGGGATCA | 9870 |
rs765662798 | snp | C/G | 1.75289e-05 | 0.00296043 | intron-variant | AREL1 | GRCh38.p7 | 14:74683264 | AGAGAGGGAAGGAGA[C/G]AAAGGGAAAAAGAAA | 9870 |
rs765666716 | snp | C/T | 1.66449e-05 | 0.00288482 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713023 | CGGGCTCCCCACTCT[C/T]CCACCAACAGACCCC | 9870 |
rs765704156 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663410 | AACAGGGCTGAGCCC[C/T]GTGTGCCATCTCCCT | 9870 |
rs765729129 | snp | C/T | 1.65798e-05 | 0.00287917 | intron-variant | AREL1 | GRCh38.p7 | 14:74673044 | TGTGGCTGGGCTCAC[C/T]ACCTTCCCTATAGAA | 9870 |
rs765823716 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709635 | AAGACCTCAGAAGCA[C/G]AACATGCTGTATGCC | 9870 |
rs765825680 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696142 | CAAAACTTTACTATC[C/T]GATGCTTTATTGAAA | 9870 |
rs765839415 | snp | A/T | 1.66225e-05 | 0.00288287 | intron-variant | AREL1 | GRCh38.p7 | 14:74664940 | GCTGGAAAAAGATGG[A/T]AAGGTGTTACTATGA | 9870 |
rs765842012 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697244 | GCTAGTGGCAGCAAA[C/G]AGAAGTTCTGATATC | 9870 |
rs765883001 | snp | C/T | 1.67365e-05 | 0.00289275 | intron-variant | AREL1 | GRCh38.p7 | 14:74664808 | TAACATGGCACAAAT[C/T]CAACTGAAAGAAGTT | 9870 |
rs765936922 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662696 | TGTGATAAGCACGTA[A/C]ACTCCTAGTCCCTGT | 9870 |
rs765977535 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680241 | AAGAAAAGAAAATGG[A/T]CAAAAGACACGAAGA | 9870 |
rs765980545 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703760 | GGACATTTGGGTTAC[-/A]TCCAGTTTGGTGGTA | 9870 |
rs766049069 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709154 | ATTTAAAAGGTAAAA[C/T]GGTCAGGCACAGTGG | 9870 |
rs766078933 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674347 | GCTCACATCTATAAT[C/T]TCAGCACTTTGGGAG | 9870 |
rs766081033 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688590 | TACTTTTTCCCCAAA[A/C]AACTGTCTTCTTGAA | 9870 |
rs766116303 | snp | A/G | 3.31208e-05 | 0.00406931 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683390 | CTTGCGCACAGTGAA[A/G]GCCACTTTTACTACG | 9870 |
rs766118763 | snp | C/T | 4.97517e-05 | 0.00498732 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684578 | GTCCGGTCCCCTCGG[C/T]GCTCGCGGTCCTCAT | 9870 |
rs766143637 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668806 | TTATCATTTGATGCT[A/G]TTTAACACCACAATG | 9870 |
rs766165473 | snp | C/G | 3.34706e-05 | 0.00409074 | intron-variant | AREL1 | GRCh38.p7 | 14:74683292 | AAAGGAAAAAAGAAC[C/G]TACCAGGTTGAAAAA | 9870 |
rs766221110 | snp | A/G | 1.64746e-05 | 0.00287002 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713239 | GGACGTTATCAGGCC[A/G]CTTTTTGGGTGGAGA | 9870 |
rs766241366 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700594 | CCATTCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 9870 |
rs766250737 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689230 | TCTGTAAGCATGTTC[C/T]GACCCTGTTGGGGGC | 9870 |
rs766296374 | snp | C/T | 0.000116087 | 0.00761775 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670821 | TGGTATCAAATAGTG[C/T]TTTGCAGATTAGCTC | 9870 |
rs766317022 | snp | A/C/G | 3.32907e-05 | 0.00407976 | missense, stop-gained | AREL1 | GRCh38.p7 | 14:74667498 | CCTCCTCTTTCACTT[A/C/G]ACTGGCCAGCCGATA | 9870 |
rs766338378 | snp | G/T | 3.31351e-05 | 0.00407019 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676185 | TTATTGATTGGCTGA[G/T]TTTGGTATGAAATGC | 9870 |
rs766352833 | snp | C/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714468 | TTACATTTTAGCCCT[C/T]TATAAGAAGCATATG | 9870 |
rs766370489 | snp | A/G | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672889 | GAATGTGGTCTTTTC[A/G]TATGTACCTGCCGAA | 9870 |
rs766394170 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694043 | TTACCCAGACATGGC[A/G]GCAGGCGCCTGTGGT | 9870 |
rs766430173 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706571 | AGAAACTCAACACTT[-/A]ACCTATTCAAAACAA | 9870 |
rs766436462 | snp | C/T | 4.97203e-05 | 0.00498575 | intron-variant | AREL1 | GRCh38.p7 | 14:74672990 | ATTACAGCCTCATTA[C/T]AAGCCATCTGTGTAG | 9870 |
rs766453616 | snp | C/T | 1.65866e-05 | 0.00287976 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676750 | TAGAAGGAACCACCA[C/T]TCCTGGAACAAAGAC | 9870 |
rs766459467 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678697 | AGACATGTATAAGCA[-/AA]AAAAAAAAAAAAAAA | 9870 |
rs766494403 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667816 | CTATTATTTCTGAAA[C/T]GGGTGCCTGGGTAAG | 9870 |
rs766565239 | snp | A/G | 1.65778e-05 | 0.002879 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684491 | TGGCCCACCTCATAG[A/G]GGTCCTTCCAATCCC | 9870 |
rs766596124 | snp | C/G | 1.76434e-05 | 0.00297008 | intron-variant | AREL1 | GRCh38.p7 | 14:74667632 | GACAAGGGAGAGGCT[C/G]TGGATGGAAATTTAT | 9870 |
rs766626623 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692848 | AGCTGGGACTACAGG[C/T]GTGCACTACCACACC | 9870 |
rs766643493 | snp | A/G | 1.68525e-05 | 0.00290275 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713595 | GATATTCTAATAAGA[A/G]TCTAGAGAGGATAAG | 9870 |
rs766652518 | in-del | -/AG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699405 | GAGAGCAAGAGCAAG[-/AG]AGAGAGAGAGAGAGA | 9870 |
rs766750492 | snp | A/G | 3.32491e-05 | 0.00407719 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685624 | AAAACATCAGGTCCC[A/G]TCAATGCCAACAGAC | 9870 |
rs766769581 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668008 | CTCAGAAATTCCAAG[A/G]TGGGAACAATTGTTC | 9870 |
rs766772477 | snp | A/C | 1.67967e-05 | 0.00289794 | upstream-variant-2KB, utr-variant-5-prime, missense | AREL1, FCF1 | GRCh38.p7 | 14:74713499 | GGGGAAGCAAAAGAA[A/C]ACAAGGAAGTATGCG | 9870 |
rs766785462 | in-del | -/GTGA | 1.66935e-05 | 0.00288903 | upstream-variant-2KB, splice-donor-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713553 | CAGAGATCAGAGGCT[-/GTGA]GTGTCTGGAATCAAC | 9870 |
rs766786700 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671884 | TCTATCCACTAGACA[C/T]ATTTATCCACAAGGC | 9870 |
rs766814268 | snp | A/G | 1.73351e-05 | 0.00294402 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670119 | GGGCGATTAGGGTTG[A/G]GATGCACCTGTCCAA | 9870 |
rs766856577 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676650 | TTGGTGGGATTATCA[C/T]ACTCATCTCGGGGTA | 9870 |
rs766865552 | snp | A/G | 1.66277e-05 | 0.00288333 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670061 | GAGACACTTGCCCAC[A/G]AGCCGTCCCGCAAAC | 9870 |
rs766882443 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698143 | TGGGCCTCTGCTCCC[A/G]GCACCAAGGAGTTAA | 9870 |
rs766887113 | snp | C/T | 3.31609e-05 | 0.00407177 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670809 | AGAGCTGATTGGTGG[C/T]ATCAAATAGTGCTTT | 9870 |
rs766946503 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663552 | ATGGGCAGGGAGCAG[A/G]TGAGGTAAAGACAAG | 9870 |
rs766951711 | in-del | -/CGTG | 1.66073e-05 | 0.00288156 | frameshift-variant, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684614 | AGGAAGCTGACTACA[-/CGTG]CGGCAAGCTCAAAGA | 9870 |
rs767005007 | snp | A/G | 1.65679e-05 | 0.00287814 | missense | AREL1 | GRCh38.p7 | 14:74663981 | CGGCAAAGCCTCCAG[A/G]TGGTAGCTGAGAGGA | 9870 |
rs767042289 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691210 | CTGCAGTCCCAGTTA[C/T]TTGGGAGGCTGAGGC | 9870 |
rs767048334 | snp | C/T | 6.77886e-05 | 0.00582149 | intron-variant | AREL1 | GRCh38.p7 | 14:74664788 | CTTCTGAAACTTTTT[C/T]CTTATAACATGGCAC | 9870 |
rs767055297 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684820 | AAACACTGCACTGGG[C/T]ACTACCTCTGTAGAT | 9870 |
rs767056134 | snp | A/C | 3.6914e-05 | 0.004296 | intron-variant | AREL1 | GRCh38.p7 | 14:74670176 | TTTTTCTTCAAGCCC[A/C]GTTCTGGAAGGACCC | 9870 |
rs767087003 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710061 | TTTTCCTCACAAGTA[G/T]GTGCCCAAAAGCAAT | 9870 |
rs767130283 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74676498 | AAGGAGAAGGAAAGA[G/T]AGATCGAAGTGAATT | 9870 |
rs767164262 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675565 | ATTTTTAACAGTTGA[A/T]AGTGGCTTTCTATAC | 9870 |
rs767212604 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662790 | TATTCTTACTGTTCT[A/C]ATCTTTTGCTACAAA | 9870 |
rs767234459 | snp | A/C | 1.71196e-05 | 0.00292567 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713481 | CTAAAATTTCTGTTT[A/C]AAGGGGAAGCAAAAG | 9870 |
rs767318841 | snp | A/T | 1.66493e-05 | 0.0028852 | intron-variant | AREL1 | GRCh38.p7 | 14:74683554 | ATGGGGAGAAGAAGG[A/T]CACCTGTTAGCAAGC | 9870 |
rs767332286 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669031 | TACCCCAGTAGCTAG[A/G]ACCACAGGCACACGC | 9870 |
rs767376617 | snp | C/G | 1.73866e-05 | 0.00294839 | intron-variant | AREL1 | GRCh38.p7 | 14:74667613 | TAACAGGCAGCAAAA[C/G]ACAGACAAGGGAGAG | 9870 |
rs767412067 | in-del | -/TTTTAT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688830 | GCCCTTCTATTTTAT[-/TTTTAT]TTTTATTTTTATTTT | 9870 |
rs767427241 | snp | A/G | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675820 | CGGCGCTGGGAAGAG[A/G]TCATGTGCATGGGTG | 9870 |
rs767431537 | snp | C/T | 1.66319e-05 | 0.00288369 | missense | AREL1 | GRCh38.p7 | 14:74667486 | GGAAATGTTCCACCT[C/T]CTCTTTCACTTGACT | 9870 |
rs767480219 | snp | C/T | 1.6588e-05 | 0.00287988 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684473 | ACTCGGAAGGCCATG[C/T]TGTGGCCCACCTCAT | 9870 |
rs767522404 | snp | A/G | 3.35053e-05 | 0.00409286 | intron-variant | AREL1 | GRCh38.p7 | 14:74676329 | GGGCCGAGCTATAGG[A/G]AGGCAACAGAGCATC | 9870 |
rs767536627 | in-del | -/CA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668066 | GTCAACAGAACAAGC[-/CA]CAGTTTGATACTTGA | 9870 |
rs767543375 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682172 | ACATGGAAAGAGAGA[C/T]GGCTTGAGAGCCACT | 9870 |
rs767544212 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701975 | CTCACATCCAGGTCA[C/T]GCTGACACAAGAGGT | 9870 |
rs767555253 | snp | C/T | 3.31181e-05 | 0.00406914 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663810 | ATATGTAGGGAGGCA[C/T]AGCTGGTTAAAACTG | 9870 |
rs767562641 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702863 | GCTAAAGCATAACAA[C/G]AGTGACCTTTGCTCC | 9870 |
rs767591465 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668142 | ACCTTTGGTTAATTG[C/T]CCCTCCAGACCTTAG | 9870 |
rs767717273 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694152 | TGCACTCCACCCTGG[A/G]CAACAGAGCCAGACC | 9870 |
rs767735826 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680576 | AAATTTATGTTCACA[C/T]AAAAACCTGTAAGTG | 9870 |
rs767742266 | snp | C/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714560 | TTTACCCATTGCTTG[C/G]AAGTGGATTGTGATC | 9870 |
rs767762566 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666300 | TAGTAACTTGCACTG[C/T]ACCATTTTGTACTGA | 9870 |
rs767788047 | in-del | -/AATAT | 3.33322e-05 | 0.00408228 | intron-variant | AREL1 | GRCh38.p7 | 14:74685567 | AGCAACCTTTACAAA[-/AATAT]AATAGAGAGAGCTCT | 9870 |
rs767852029 | snp | A/T | 1.66288e-05 | 0.00288343 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685603 | TCCATAACGTACCAA[A/T]AACGTAAAACATCAG | 9870 |
rs767864634 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693939 | CCCAGCACTTTGGGA[A/G]GCCAAGGCAGGCGGA | 9870 |
rs767871926 | snp | C/T | 3.37029e-05 | 0.00410492 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669970 | GCATACGCAGTCCTA[C/T]GATTTGGGCCAGGAA | 9870 |
rs767900112 | snp | A/G | 0.000186759 | 0.0096615 | intron-variant | AREL1 | GRCh38.p7 | 14:74672041 | GAATGTAAGAACTAT[A/G]CCAGTGTCTGTGCAG | 9870 |
rs767983612 | snp | A/C | 1.65603e-05 | 0.00287747 | missense | AREL1 | GRCh38.p7 | 14:74663724 | CAGGAGAGTGGTCAG[A/C]GCATGCCAAAGCCCT | 9870 |
rs768012663 | snp | C/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661249 | AAAGCAGCCACTCAC[C/T]CCTTAGTTCTTTTAA | 9870 |
rs768035474 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686322 | CTCAGTCATGCCTGT[C/T]AAGGTAGGAGTCTGA | 9870 |
rs768107446 | snp | C/T | 3.347e-05 | 0.00409071 | missense | AREL1 | GRCh38.p7 | 14:74667551 | AAGATTTTATTCGCA[C/T]TGGTGACTGGAGTTT | 9870 |
rs768114538 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713996 | AAATGGGAAAACTCC[A/G]AGATATCTCCATTTT | 9870 |
rs768142006 | snp | A/G | 1.66023e-05 | 0.00288113 | synonymous-codon, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669657 | TTCTCACCTTATCCA[A/G]TTGACCTGATTTATT | 9870 |
rs768152171 | snp | A/G | 1.6599e-05 | 0.00288084 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667348 | CATCAAAAATAGCCA[A/G]AAGGTTCTCAGGGAC | 9870 |
rs768163481 | snp | G/T | 1.6696e-05 | 0.00288924 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713555 | GAGATCAGAGGCTGT[G/T]AGTGTCTGGAATCAA | 9870 |
rs768164715 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687946 | CTATTCTAATTTTAT[A/G]CCTAAAAAATTTTAC | 9870 |
rs768176993 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74676788 | TCTAACATTTATTTA[-/T]TTTATTTTTTTATTT | 9870 |
rs768223276 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681177 | GGTGACAGAGCAAGG[C/T]CCTGTCTCAAAAACA | 9870 |
rs768335540 | snp | C/T | 1.66007e-05 | 0.00288098 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673110 | AGCGGATAAAAGTGG[C/T]TGCTAGAATGTTCCT | 9870 |
rs768424253 | in-del | -/GAGA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699377 | TGTGTGTGTGTGTGT[-/GAGA]GAGAGAGAGAGAGAG | 9870 |
rs768427911 | in-del | -/G | 0.000161355 | 0.00898063 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712940 | AACGTTACCCGAGCC[-/G]GGGGTTGCAGCGCGA | 9870 |
rs768488831 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679664 | AAACCCCATCTCTAC[C/T]AAAAACACAAAAAAC | 9870 |
rs768499778 | snp | C/G | 0.000175948 | 0.00937779 | splice-donor-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712932 | TGGAGAGAAACGTTA[C/G]CCGAGCCGGGGGTTG | 9870 |
rs768507976 | snp | A/C/T | 3.31171e-05 | 0.00406911 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663919 | GTGTGCAGTAGGCAG[A/C/T]GTGCTATGGGTCGGA | 9870 |
rs768510714 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701893 | GGCTGCAGGGCCCAT[A/G]CAAGTCCAAAATCCA | 9870 |
rs768514896 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669921 | GGCCAGGGGCCTTAG[A/T]AGGAAATGCACACCC | 9870 |
rs768523211 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692413 | ATCAAAGAGAAGGTA[C/G]AACAGGCAGTGGAAA | 9870 |
rs768575538 | snp | G/T | 1.65641e-05 | 0.00287781 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675755 | CCTTCTCAGGGGTGT[G/T]GCACTCAGAGGGCGA | 9870 |
rs768621485 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672327 | AGAAGAACAGACATA[A/T]GTAAAGAGAGAAATT | 9870 |
rs768642851 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704935 | ACAAGAATTTTTTAA[A/C]ACTCCTGCATTCCAT | 9870 |
rs768682759 | snp | A/G | 1.65647e-05 | 0.00287786 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672945 | GTCCTGAAAGGTCTC[A/G]GAGCCTCCTGGGGAA | 9870 |
rs768722300 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699578 | AATCTTTCTTATACA[C/T]ACTGCTCTCATTTAT | 9870 |
rs768748320 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671172 | GAACTCTCTCTCCAA[A/G]TCCCTGTATGTCTGT | 9870 |
rs768794058 | snp | A/G | 1.88248e-05 | 0.0030679 | intron-variant | AREL1 | GRCh38.p7 | 14:74674141 | GACAGGAAATGAAGT[A/G]AATGATAAATAAAAA | 9870 |
rs768813013 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665014 | AGTTAACAGGCAAAA[C/T]GTAGAAGAAAACATT | 9870 |
rs768833093 | snp | A/T | 1.66402e-05 | 0.00288441 | intron-variant | AREL1 | GRCh38.p7 | 14:74667315 | CTGAATTGCAATCAC[A/T]TACCTCAAGCTCATT | 9870 |
rs768842320 | snp | A/G | 1.71129e-05 | 0.00292509 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670103 | CAGGCGCAGATGAGC[A/G]GGGCGATTAGGGTTG | 9870 |
rs768846580 | snp | C/T | 3.31186e-05 | 0.00406918 | missense | AREL1 | GRCh38.p7 | 14:74663796 | TCTTCATAGGAGTCA[C/T]ATGTAGGGAGGCACA | 9870 |
rs768933610 | in-del | -/TTTTATTTTTTTAT | 0.000169886 | 0.00921488 | intron-variant | AREL1 | GRCh38.p7 | 14:74676788 | TCTAACATTTATTTA[-/TTTTATTTTTTTAT]TTTTATTTTTTTTGA | 9870 |
rs768976645 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710641 | AATGGCAGCTTGACA[A/G]AGACAAGCTGCTCCA | 9870 |
rs769009018 | snp | A/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714753 | TAACATGAGGATATC[A/T]CAAAGTAGGATTTCT | 9870 |
rs769063450 | snp | A/G | 4.9879e-05 | 0.0049937 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671460 | CCAATCTGAGATGGA[A/G]AAATTCCGAGTGGCT | 9870 |
rs769088691 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683379 | TAACGCCCAGCCTTG[C/T]GCACAGTGAAGGCCA | 9870 |
rs769105384 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709371 | ATTAAATAAATATTA[C/T]ACAACAGTACTCTGA | 9870 |
rs769118550 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703601 | AAAATGTAGTCCTTC[A/G]TGTGTAGCATTTTTT | 9870 |
rs769119100 | snp | C/G | 1.65864e-05 | 0.00287974 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664923 | AGTCCCACACATCAG[C/G]AGCTGGAAAAAGATG | 9870 |
rs769130650 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688376 | CAAATTAGAACATGA[C/G]AGCCACAGTCCAGTT | 9870 |
rs769171072 | snp | A/C | 1.64894e-05 | 0.00287131 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713117 | CGCTTCCGGGCTATC[A/C]TTTGCCGGAAGCAGT | 9870 |
rs769188283 | in-del | -/TGTGTGTGTGTGAGAG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699366 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGAGAG]AGAGAGAGAGAGAGC | 9870 |
rs769198582 | snp | A/G | 3.31334e-05 | 0.00407009 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683492 | AACTCTTAGTCCCAC[A/G]GGCCGATGTGCAGGG | 9870 |
rs769220513 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690635 | GAAATTATTTTGGAA[C/T]TTTCCCAAGTCTAAT | 9870 |
rs769233140 | snp | A/C | 1.65737e-05 | 0.00287864 | intron-variant | AREL1 | GRCh38.p7 | 14:74667412 | TTAAAGTCATACCCA[A/C]ACCATGGATACAGGT | 9870 |
rs769248036 | snp | C/T | 4.96899e-05 | 0.00498422 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672853 | AACAAGGCATGTCTG[C/T]TGACCTTCAGGGTGA | 9870 |
rs769280632 | snp | A/G | 0.000343348 | 0.0130979 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713078 | GAACCGGCTCGGGGG[A/G]TTGCCCTTTCCCCAA | 9870 |
rs769282593 | snp | A/G | 1.65638e-05 | 0.00287778 | stop-gained, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672911 | CCTGCCGAAGCTCTC[A/G]CTGGAAAAAGTTCAC | 9870 |
rs769315614 | snp | C/G | 0.000183304 | 0.00957176 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713536 | AAGCGAATGCTTAGT[C/G]TCAGAGATCAGAGGC | 9870 |
rs769386343 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679973 | TTGAGCTCAGGATTT[C/T]GAGACCTGCCTGGCC | 9870 |
rs769418362 | snp | A/G/T | 1.68136e-05 | 0.0028994 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669613 | CTACAGGAAACTGGA[A/G/T]AACATAGGACCCAGA | 9870 |
rs769484590 | snp | A/G | 3.33533e-05 | 0.00408357 | intron-variant | AREL1 | GRCh38.p7 | 14:74684430 | GAAACCCCAATGGGT[A/G]TGGAGACAGAAACAT | 9870 |
rs769537759 | snp | A/G | 0.000145051 | 0.00851496 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713454 | TGCCGTGTGTTTCCA[A/G]CTTTTTTAATTCTAA | 9870 |
rs769566511 | snp | C/T | 3.31175e-05 | 0.00406911 | missense | AREL1 | GRCh38.p7 | 14:74663787 | CTGTGCACCTCTTCA[C/T]AGGAGTCATATGTAG | 9870 |
rs769586939 | snp | A/G | 3.34052e-05 | 0.00408674 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676319 | TTCTTCTTGAGGGCC[A/G]AGCTATAGGAAGGCA | 9870 |
rs769591946 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665519 | AGCCTGGGAATATCA[A/T]GGAGAAAAGGCAAGC | 9870 |
rs769615085 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668783 | TTACTGCAACTTTAG[C/T]GTCATCATTATCATT | 9870 |
rs769621448 | in-del | -/T | 1.64894e-05 | 0.00287131 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713117 | GCTTCCGGGCTATCC[-/T]TTTGCCGGAAGCAGT | 9870 |
rs769634579 | snp | G/T | 1.66054e-05 | 0.00288139 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670023 | ACCAACTGCTTGTAG[G/T]CTCCTCCTAGAGAGG | 9870 |
rs769643137 | snp | A/G | 1.65594e-05 | 0.0028774 | intron-variant | AREL1 | GRCh38.p7 | 14:74663887 | GCATGCATCAGGCGG[A/G]CAGATACCTACCATG | 9870 |
rs769666160 | snp | A/G | 1.66377e-05 | 0.00288419 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685653 | ACAGCCGAGGATCAC[A/G]GCTGCAGCTGTTAAA | 9870 |
rs769686196 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707275 | CGGGAGGCTGAGGCC[A/G]GAGAATAGTTTGAAC | 9870 |
rs769710771 | snp | A/C | 9.93641e-05 | 0.00704785 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683468 | TGCTAGCTCGACATG[A/C]GAGATGTGAACTCTT | 9870 |
rs769718445 | snp | A/C | 3.33489e-05 | 0.0040833 | intron-variant | AREL1 | GRCh38.p7 | 14:74685563 | CCCAAGCAACCTTTA[A/C]AAAAATATAATAGAG | 9870 |
rs769736747 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681571 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCCA | 9870 |
rs769774830 | snp | C/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660778 | TTTTGTTTGCCACTC[C/T]CAAACCCCTTGTGGG | 9870 |
rs769794302 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668974 | CCTTAACCTCCTGGG[C/T]TCAAGCGATGTTCCA | 9870 |
rs769797690 | in-del | -/T | 1.71752e-05 | 0.00293041 | intron-variant | AREL1 | GRCh38.p7 | 14:74675672 | GTTCAAGCAGGGGGA[-/T]TTTATGTCGAGAATG | 9870 |
rs769807804 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679368 | TCAAGGCTGCAGTGA[A/G]CCATGACTATGCTAC | 9870 |
rs769826629 | snp | C/T | 1.6623e-05 | 0.00288292 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676587 | AGACTGCTTACCTCA[C/T]GAATGGACAAGGTGT | 9870 |
rs769827949 | snp | A/G | 3.57207e-05 | 0.004226 | intron-variant | AREL1 | GRCh38.p7 | 14:74673994 | GATAGTCCAGAGATG[A/G]AGCATGCTTGATGTG | 9870 |
rs769835360 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693843 | TAAGTTGGCAAACTT[G/T]TATCATTAAAAATAA | 9870 |
rs769864685 | snp | C/T | | | missense, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669668 | TCCAATTGACCTGAT[C/T]TATTATATTTCTCTT | 9870 |
rs769933526 | snp | G/T | 4.968e-05 | 0.00498373 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683368 | CTGTGATTTCATAAC[G/T]CCCAGCCTTGCGCAC | 9870 |
rs769940954 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686879 | GGTGCTCCCAAAAGG[G/T]TCTATTACAGACAAT | 9870 |
rs769951710 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673683 | CAATGTATTTTAATA[A/T]ATGAGAGTGGTGCTT | 9870 |
rs769970780 | snp | A/C | 3.38553e-05 | 0.00411418 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674094 | GATCTTCAGGTAGAA[A/C]TCCTTCACTGAGAAT | 9870 |
rs769979686 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685951 | ACATGGCTTTCATCT[G/T]CTTAGATCCATAGTT | 9870 |
rs770014189 | snp | C/G | 1.69095e-05 | 0.00290765 | splice-acceptor-variant | AREL1 | GRCh38.p7 | 14:74670872 | CTCCCCAGTCCAGAG[C/G]TGAAAAGCATAATGA | 9870 |
rs770062986 | snp | A/G | 1.66718e-05 | 0.00288715 | intron-variant | AREL1 | GRCh38.p7 | 14:74667303 | AAGAATGGGAGTCTG[A/G]ATTGCAATCACTTAC | 9870 |
rs770063917 | snp | A/C | 5.07438e-05 | 0.0050368 | intron-variant | AREL1 | GRCh38.p7 | 14:74676114 | GGCTGAAGAACAGCA[A/C]TAAATCATACTTTTC | 9870 |
rs770171797 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667104 | TCATTTATTTATCCC[C/T]TAAGCTAATATCTCT | 9870 |
rs770230379 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712545 | GCTTCACAATAAATG[C/T]GCATTGTATCTCACC | 9870 |
rs770239384 | snp | A/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711574 | AAAATAAAATAAAAT[A/T]GGCATAAAATTCCAA | 9870 |
rs770255987 | snp | G/T | 2.23446e-05 | 0.00334243 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713060 | GGTCTCCACCCGGCC[G/T]GGGAACCGGCTCGGG | 9870 |
rs770286457 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704544 | TCGGTAGGCAGGGGA[C/T]GACTCTGAACAGAAT | 9870 |
rs770333923 | snp | A/G | 3.33556e-05 | 0.00408371 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713097 | CCCTTTCCCCAAGGA[A/G]TTTCCGCTTCCGGGC | 9870 |
rs770359342 | in-del | -/GT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699348 | AAGTGACAGTGAGGG[-/GT]GTGTGTGTGTGTGTG | 9870 |
rs770362067 | snp | A/C | 0.000116209 | 0.00762173 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676284 | GTTACTGATTTCTCA[A/C]ATGAGACACCAGTAC | 9870 |
rs770374557 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74692005 | TCCATGTTGTACATC[C/T]CAATAACTAAAGCTT | 9870 |
rs770390350 | snp | A/G | 1.67508e-05 | 0.00289398 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671481 | CCGAGTGGCTTTCAG[A/G]GACTGAAAAGAAGTG | 9870 |
rs770401840 | snp | C/T | 3.31417e-05 | 0.00407059 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664911 | ACTGATGTCTCCAGT[C/T]CCACACATCAGCAGC | 9870 |
rs770436027 | snp | A/T | 1.68949e-05 | 0.0029064 | intron-variant | AREL1 | GRCh38.p7 | 14:74676549 | AAGGAGCCAGCTCTC[A/T]CTAGCACACAGATAA | 9870 |
rs770453473 | snp | A/G | | | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676315 | TCTCTTCTTCTTGAG[A/G]GCCGAGCTATAGGAA | 9870 |
rs770551811 | snp | C/T | 1.6566e-05 | 0.00287797 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672837 | TTTACCTACCGATTC[C/T]AACAAGGCATGTCTG | 9870 |
rs770551853 | snp | C/T | 1.66117e-05 | 0.00288194 | missense | AREL1 | GRCh38.p7 | 14:74667333 | CCTCAAGCTCATTCT[C/T]ATCAAAAATAGCCAA | 9870 |
rs770603866 | snp | A/T | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713174 | CGTTGGTGATTACGG[A/T]AGAACCAGGAGTTTG | 9870 |
rs770604549 | snp | C/T | 1.65592e-05 | 0.00287738 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663783 | CATCCTGTGCACCTC[C/T]TCATAGGAGTCATAT | 9870 |
rs770647133 | in-del | -/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712580 | CTTGGCTTGGGTAAG[-/T]TAGTAACATATGCAA | 9870 |
rs770650622 | snp | A/T | | | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669633 | TAGGACCCAGAGGCT[A/T]TGTCCTCTTTCTCAC | 9870 |
rs770653134 | snp | A/C/T | 0.000209759 | 0.010239 | intron-variant | AREL1 | GRCh38.p7 | 14:74670885 | AGCTGAAAAGCATAA[A/C/T]GAAAATAAAAAATGA | 9870 |
rs770691364 | snp | A/C/G | 4.96992e-05 | 0.00498473 | missense, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669693 | TCTCTTCTGCAAAGA[A/C/G]CAGCTCCATCTCACT | 9870 |
rs770818302 | snp | G/T | 1.79303e-05 | 0.00299413 | intron-variant | AREL1 | GRCh38.p7 | 14:74673988 | GGCTGAGATAGTCCA[G/T]AGATGAAGCATGCTT | 9870 |
rs770819687 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695708 | AATTATTTGTTTATA[C/T]AGCAGTCTCTCCTAA | 9870 |
rs770836034 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74708937 | TATGGTGCTGTAACA[C/T]CATATCAACAGCTCA | 9870 |
rs770850438 | in-del | -/CTA | 2.89147e-05 | 0.00380217 | intron-variant | AREL1 | GRCh38.p7 | 14:74664119 | CACACAGTAAACAAG[-/CTA]GGATTAGATCCCTGG | 9870 |
rs770857054 | snp | A/G | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661166 | CAGGAGGAATTCCTG[A/G]GGAAATGCAAAATCA | 9870 |
rs770858865 | snp | A/G | 1.65663e-05 | 0.002878 | missense | AREL1 | GRCh38.p7 | 14:74664877 | CAACAACTACTGCAT[A/G]GGCTTTGAAGTCAGA | 9870 |
rs770872126 | snp | A/G | 5.36841e-05 | 0.00518065 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714955 | AAGTGTGAGTAATCA[A/G]ACGTTTGAAGTTTTC | 9870 |
rs770926001 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696638 | TCACTTGAGCCTAGG[A/G]GTTGAAACCAGACTG | 9870 |
rs770934838 | in-del | -/ACCTCC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695160 | CACTGCCTCACTACA[-/ACCTCC]ACCTCCTGGGTTCAA | 9870 |
rs770949348 | snp | A/C/G | 0.000117055 | 0.00764951 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684656 | ATTGTGAAGAAGAAT[A/C/G]CAACCACAGACACTG | 9870 |
rs771030739 | snp | C/T | 1.6607e-05 | 0.00288153 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673168 | TTGAATGCCATCATC[C/T]ACCACCAGTGTGAGC | 9870 |
rs771058472 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707202 | GTGAAATCCCATCTC[A/T]ACTAAAAATACAAAA | 9870 |
rs771072648 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674908 | GCTGGAGTGGAATAT[C/G]TTGGTGGTATAGGGG | 9870 |
rs771073965 | snp | G/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662115 | GTATAGAGACCCTGA[G/T]GCTGGATCCCGGACC | 9870 |
rs771114087 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683354 | TCCACCAAGCTTCAC[C/T]GTGATTTCATAACGC | 9870 |
rs771203415 | snp | A/C | 3.33845e-05 | 0.00408548 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670863 | GGCGAGGCCCTCCCC[A/C]GTCCAGAGCTGAAAA | 9870 |
rs771216600 | snp | A/T | 1.65734e-05 | 0.00287862 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684529 | TTTGCAAGACCGGGG[A/T]TCCAGGTAATTTCCC | 9870 |
rs771252406 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686968 | ATCTCTTGGGACCCT[A/G]TGCTGAATTAGCTGG | 9870 |
rs771331237 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712698 | TCGAGAACAATCATC[C/T]ACCTAGCTGCACAAA | 9870 |
rs771342198 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673778 | CTATTAACTTAGTCT[A/T]GAAGGCAAAGGATCA | 9870 |
rs771344102 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688176 | CATTACAGGTGCCTG[C/T]CACCATGCCCAGCTA | 9870 |
rs771383141 | snp | C/T | 1.69329e-05 | 0.00290967 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675905 | AGTAAATGCTCACGC[C/T]TGAAGTGGACACATT | 9870 |
rs771416183 | snp | A/G | 3.38438e-05 | 0.00411349 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713009 | CACTCAGCAGAAGAC[A/G]GGCTCCCCACTCTCC | 9870 |
rs771427288 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693515 | CTAATTAGTAAATGA[A/G]GAGACAGTCTTACCA | 9870 |
rs771440340 | snp | A/G | 3.31225e-05 | 0.00406941 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675777 | AGAGGGCGAGTCTTC[A/G]TCTTCCTCGTCAACA | 9870 |
rs771476721 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713678 | AGATTTATATAGCAT[A/G]AGATAGCCAGTGTTT | 9870 |
rs771502885 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679347 | GATCACCTAAGCCGG[A/G]AGAGGTCAAGGCTGC | 9870 |
rs771544577 | snp | G/T | 3.32358e-05 | 0.00407637 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670771 | ACTCACTAATGCTTG[G/T]TTGTTGTCACTGAAC | 9870 |
rs771562343 | snp | C/G | 1.66774e-05 | 0.00288763 | intron-variant | AREL1 | GRCh38.p7 | 14:74685554 | CAAAAAGGACCCAAG[C/G]AACCTTTACAAAAAT | 9870 |
rs771573679 | snp | C/T | 1.66416e-05 | 0.00288453 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684637 | AAGCTCAAAGAGGAA[C/T]TTAATTGTGAAGAAG | 9870 |
rs771619038 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661879 | TCTCTGGAAGGCTGC[C/T]GGAGGGGAGAATTCA | 9870 |
rs771646809 | snp | A/G | 3.31279e-05 | 0.00406975 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663670 | ATGTCTGTAACTTGC[A/G]CCCAGAAGCTCCAGA | 9870 |
rs771680192 | snp | C/T | 3.31543e-05 | 0.00407137 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676263 | TGGAAAGTCTGCCTG[C/T]TGGATGTTACTGATT | 9870 |
rs771694838 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74676893 | GCTCTGCCTTCCGGG[C/T]TCATGCCATTCTCCT | 9870 |
rs771705258 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671010 | TGCGACTCATCTAAA[C/T]TGTGGTCCTTTAGAA | 9870 |
rs771774541 | snp | C/T | 1.65688e-05 | 0.00287821 | intron-variant | AREL1 | GRCh38.p7 | 14:74672976 | CAGCAAGATCCATCA[C/T]TACAGCCTCATTACA | 9870 |
rs771813159 | in-del | -/TA | 1.65776e-05 | 0.00287898 | frameshift-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669672 | ATTGACCTGATTTAT[-/TA]TATTTCTCTTCTGCA | 9870 |
rs771832759 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704894 | TAAACGTTTCACAAG[A/G]GAAAATCCTCTCGTC | 9870 |
rs771858655 | snp | A/G | 1.66045e-05 | 0.00288132 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673149 | AGCTGAGCTCCACAG[A/G]AGGTTGAATGCCATC | 9870 |
rs771901257 | snp | A/G | 2.57775e-05 | 0.00359 | upstream-variant-2KB, missense, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714939 | GCATTAAAGGAAAGA[A/G]AAGTGTGAGTAATCA | 9870 |
rs771912272 | snp | C/T | 0.0003996 | 0.0141294 | intron-variant | AREL1 | GRCh38.p7 | 14:74678370 | AAGCACGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 9870 |
rs771930678 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672233 | ACCCATTCAGTAGAT[C/T]TGAAGGCCAGTAAGT | 9870 |
rs771957375 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703714 | CATTAAATGGACATA[A/C]TGCAATCTGTTTATC | 9870 |
rs771974228 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683073 | GGGGAAAAGTGACTA[C/T]TAACATGTATGGGGT | 9870 |
rs771982218 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711699 | GTTAACTATGAATAA[-/AC]ATAAGTCCTGATAAC | 9870 |
rs772033316 | in-del | -/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700429 | AAAGAACTTCCAGAA[-/G]GGGGGGAAAAAGATA | 9870 |
rs772045790 | in-del | -/TGG | 3.3123e-05 | 0.00406945 | cds-indel, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676636 | AGGACATGGAATTGT[-/TGG]TGGGATTATCATACT | 9870 |
rs772062309 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684322 | TGACTCTTCAGATAG[C/T]AGCAATTCACTAGTT | 9870 |
rs772097652 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698883 | AAAAAAAAAAGCTGG[G/T]TGTGGTGGTATGCAC | 9870 |
rs772098210 | snp | A/G | 1.67323e-05 | 0.00289239 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713570 | GAGTGTCTGGAATCA[A/G]CTGCCCAGGGATATT | 9870 |
rs772108958 | snp | C/T | 1.65732e-05 | 0.00287859 | missense, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669677 | CCTGATTTATTATAT[C/T]TCTCTTCTGCAAAGA | 9870 |
rs772114316 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669829 | CTTGCCCTGAAAGGT[A/G]TAACTGCTTAGAACC | 9870 |
rs772142931 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710601 | AGATACATCAAAAAA[C/G]TGGTTGCTATTAGCT | 9870 |
rs772177718 | in-del | -/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678161 | TGAAAAAGAAGAATA[-/C]AAGTGGAGTCAGCTT | 9870 |
rs772191654 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709237 | AGGCCAGGAGTTCAA[C/G]ATCAGCCTGGGCAAC | 9870 |
rs772203633 | snp | A/G | 1.80958e-05 | 0.00300792 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664054 | CAGACTGGAAACCAC[A/G]GTCCAAAACCACCTC | 9870 |
rs772224371 | snp | C/T | 3.47717e-05 | 0.00416949 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675929 | ACACATTGCGTTCGA[C/T]GATATTCTTCTCATC | 9870 |
rs772255519 | snp | A/G | 1.71675e-05 | 0.00292976 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670108 | GCAGATGAGCGGGGC[A/G]ATTAGGGTTGGGATG | 9870 |
rs772277015 | snp | A/C | 2.51911e-05 | 0.00354893 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713053 | CAGAGTTGGTCTCCA[A/C]CCGGCCTGGGAACCG | 9870 |
rs772327957 | snp | C/T | 0.000409361 | 0.0143008 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712966 | CGCGACGAAGTTCCA[C/T]CTCCGCTGTCCTGGG | 9870 |
rs772329088 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707487 | CTAAAATGGTGAAAT[C/T]CCATCTCTACTAAAA | 9870 |
rs772438197 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701303 | TGCTGCTGTTAAAGA[C/T]GTATCAGAGACTGGT | 9870 |
rs772461128 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662217 | GCAGGAACTGTAGCA[A/G]CTCAGGAGGGCTTGT | 9870 |
rs772494627 | snp | A/G | 3.31505e-05 | 0.00407113 | intron-variant | AREL1 | GRCh38.p7 | 14:74667422 | ACCCACACCATGGAT[A/G]CAGGTATTTTAACTT | 9870 |
rs772506494 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674942 | GTCCTCACACAAAAA[A/T]GTTCATACAAAAGAG | 9870 |
rs772511504 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687142 | CGATCTGACCCTAGA[C/T]GTGAAATTTCTGGTC | 9870 |
rs772513931 | snp | C/T | 2.10236e-05 | 0.00324213 | intron-variant | AREL1 | GRCh38.p7 | 14:74674159 | TGATAAATAAAAAGG[C/T]TCTATTTGGGTATTC | 9870 |
rs772567310 | snp | A/G | 1.65839e-05 | 0.00287953 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683510 | CCGATGTGCAGGGAA[A/G]GGCTGCCCGTTCTTA | 9870 |
rs772633684 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702347 | CTCAAACCTCAGTTC[C/T]TGACTTCTGTGCACC | 9870 |
rs772678977 | snp | A/G | 1.65971e-05 | 0.00288067 | intron-variant | AREL1 | GRCh38.p7 | 14:74664930 | CACATCAGCAGCTGG[A/G]AAAAGATGGTAAGGT | 9870 |
rs772686619 | snp | A/T | 1.65748e-05 | 0.00287874 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676172 | GTCAAATTCACCATT[A/T]TTGATTGGCTGATTT | 9870 |
rs772750295 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688396 | ACAGTCCAGTTATCA[C/T]GAAGCTGGCAGTAAT | 9870 |
rs772793038 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701579 | AACACATGAGAATTA[C/T]GGGAACTATAATTCA | 9870 |
rs772820644 | in-del | -/G | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713147 | TATGTGAATGACGTA[-/G]AAGTATTGCGCCGTT | 9870 |
rs772849447 | snp | C/T | 1.65644e-05 | 0.00287783 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663671 | TGTCTGTAACTTGCG[C/T]CCAGAAGCTCCAGAG | 9870 |
rs772871363 | snp | A/G | 1.67618e-05 | 0.00289493 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713577 | TGGAATCAACTGCCC[A/G]GGGATATTCTAATAA | 9870 |
rs772873794 | in-del | -/AGA | 1.66288e-05 | 0.00288343 | intron-variant | AREL1 | GRCh38.p7 | 14:74683545 | ATAACTGCCATGGGG[-/AGA]AGAAGGACACCTGTT | 9870 |
rs772906421 | snp | C/T | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673163 | GGAGGTTGAATGCCA[C/T]CATCCACCACCAGTG | 9870 |
rs772947961 | snp | C/G | 3.29734e-05 | 0.00406025 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713123 | CGGGCTATCCTTTGC[C/G]GGAAGCAGTATGTGA | 9870 |
rs772954430 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693859 | TATCATTAAAAATAA[A/G]TAAGTATATGTATTT | 9870 |
rs773017657 | snp | A/G | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74660950 | GAATTTCTAGGTAGT[A/G]AAACAACAATGAATT | 9870 |
rs773056488 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74680124 | GAGGTTGGTTGCAGT[C/G]AGTCAAGGTAGCACC | 9870 |
rs773063747 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707300 | TTGAACCCAGGAGGC[A/C]GAAGTGGCAGTGAGC | 9870 |
rs773092700 | snp | C/T | 5.28779e-05 | 0.00514161 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675944 | CGATATTCTTCTCAT[C/T]CTCTGAAGTATAATA | 9870 |
rs773110486 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681620 | TCTACTAAAAATACA[A/C]AAATTAGCTGGGCGT | 9870 |
rs773160175 | snp | A/C | 1.74254e-05 | 0.00295168 | intron-variant | AREL1 | GRCh38.p7 | 14:74667616 | CAGGCAGCAAAAGAC[A/C]GACAAGGGAGAGGCT | 9870 |
rs773195025 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667756 | ACACTTGGTTTAATT[C/T]AGTTCCTAAGCTTCA | 9870 |
rs773209700 | in-del | -/AAAAAAAAAAAAAAAAAAAA | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712039 | TGGAAGACAAAGTGC[-/AAAAAAAAAAAAAAAAAAAA]AAAAAAAAAGAAAAA | 9870 |
rs773242655 | snp | A/G | 3.54001e-05 | 0.00420699 | intron-variant | AREL1 | GRCh38.p7 | 14:74683249 | ACAGGATGGAAAGAG[A/G]GAGAGGGAAGGAGAC | 9870 |
rs773243525 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705127 | TCACCGCAACCTCCA[C/T]CTTCCAGGTTCAAGC | 9870 |
rs773326414 | snp | C/T | 3.31378e-05 | 0.00407036 | synonymous-codon, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669685 | ATTATATTTCTCTTC[C/T]GCAAAGACCAGCTCC | 9870 |
rs773338137 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74706649 | ATTTCTTCAAATGCA[C/T]ATTAAGAAGCGACCA | 9870 |
rs773423559 | in-del | -/GA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699379 | TGTGTGTGTGTGTGA[-/GA]GAGAGAGAGAGAGAG | 9870 |
rs773436309 | in-del | -/AAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690265 | CAAGACCCTGTCTCC[-/AAA]AAAAAAAAAAAAAAA | 9870 |
rs773529888 | snp | C/T | 7.71888e-05 | 0.00621196 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664066 | CACAGTCCAAAACCA[C/T]CTCATGACCTGGCAG | 9870 |
rs773537772 | snp | C/G | 1.724e-05 | 0.00293594 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670113 | TGAGCGGGGCGATTA[C/G]GGTTGGGATGCACCT | 9870 |
rs773540091 | snp | A/C | 3.31587e-05 | 0.00407164 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676744 | TGGTCTTAGAAGGAA[A/C]CACCATTCCTGGAAC | 9870 |
rs773619380 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712629 | TAGCGATAGTCTAGG[C/T]CCTCAAACACTGCTT | 9870 |
rs773658979 | snp | G/T | 0.000278396 | 0.0117949 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692295 | TTCTCTCTAGTGCAG[G/T]GTGCAATCGACTGCC | 9870 |
rs773691883 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677752 | GTAATTTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 9870 |
rs773692313 | snp | A/G | 3.46314e-05 | 0.00416107 | intron-variant | AREL1 | GRCh38.p7 | 14:74675653 | AAATACCAATTACAC[A/G]CAGGTTCAAGCAGGG | 9870 |
rs773706278 | snp | C/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663426 | GTGTGCCATCTCCCT[C/G]AGCTACTGAGATCTT | 9870 |
rs773816363 | snp | C/T | 1.65776e-05 | 0.00287898 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684561 | GCACGTAGTCATAAA[C/T]AGTCCGGTCCCCTCG | 9870 |
rs773838767 | snp | C/G | 1.662e-05 | 0.00288266 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670057 | CATAGAGACACTTGC[C/G]CACGAGCCGTCCCGC | 9870 |
rs773884350 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74698014 | AAATTTCATGTTAAA[C/T]CAAACTCATAGATAA | 9870 |
rs773911361 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691118 | AGCTCAAGAGCTTGG[A/G]ACCAGCCTGAGCAAC | 9870 |
rs773954344 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693606 | TTTTAACACAGATAC[-/A]ATTATCCCTATTTTA | 9870 |
rs773983593 | snp | A/T | 3.36428e-05 | 0.00410125 | intron-variant | AREL1 | GRCh38.p7 | 14:74676121 | GAACAGCACTAAATC[A/T]TACTTTTCTTTTAAC | 9870 |
rs773991226 | snp | A/G | 1.65682e-05 | 0.00287817 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676724 | AGAAAAGTGGCACAC[A/G]ATTTTGGTCTTAGAA | 9870 |
rs774000856 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688648 | TATCAATTCATCATT[C/T]GCTGACATCAACTTT | 9870 |
rs774093748 | snp | A/C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682000 | CTTACAAATGCATAT[A/C/G]AATATACAATTATCA | 9870 |
rs774183690 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668818 | GCTGTTTAACACCAC[A/G]ATGTAAATAGAAGCA | 9870 |
rs774236872 | snp | G/T | 1.66999e-05 | 0.00288958 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713558 | ATCAGAGGCTGTGAG[G/T]GTCTGGAATCAACTG | 9870 |
rs774247761 | snp | A/G | | | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669723 | TCATGTCATTGTTGA[A/G]GATAAAACAAACTTT | 9870 |
rs774264865 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672872 | CCTTCAGGGTGACTT[C/T]GGAATGTGGTCTTTT | 9870 |
rs774287552 | snp | C/T | 3.3274e-05 | 0.00407871 | intron-variant | AREL1 | GRCh38.p7 | 14:74685595 | GAGCTCTTTCCATAA[C/T]GTACCAATAACGTAA | 9870 |
rs774297527 | in-del | -/AA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687961 | CCTAAAAAATTTTAC[-/AA]AATAAAGGGTTAAAA | 9870 |
rs774314378 | snp | C/T | 1.66128e-05 | 0.00288204 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670053 | GACTCATAGAGACAC[C/T]TGCCCACGAGCCGTC | 9870 |
rs774331141 | in-del | -/T | 1.65968e-05 | 0.00288065 | intron-variant | AREL1 | GRCh38.p7 | 14:74664831 | AAGAAGTTTGGTCCA[-/T]TTACCTTTTCTCTGA | 9870 |
rs774370814 | snp | A/T | 1.67775e-05 | 0.00289629 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667559 | ATTCGCATTGGTGAC[A/T]GGAGTTTGAGCTCCA | 9870 |
rs774372645 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682894 | AGCAGATGCTGGTGC[A/T]ATGCTTTTTGTACAA | 9870 |
rs774459538 | in-del | -/TGAGCTG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666058 | TCAGAAACTTTAGGC[-/TGAGCTG]TGGAGAGTTCATTTT | 9870 |
rs774572690 | snp | G/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712024 | TCAGTAGCTGGAGAA[G/T]GGAAGACAAAGTGCA | 9870 |
rs774600179 | snp | G/T | 3.31181e-05 | 0.00406914 | missense | AREL1 | GRCh38.p7 | 14:74663799 | TCATAGGAGTCATAT[G/T]TAGGGAGGCACAGCT | 9870 |
rs774626062 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679931 | CTGTAATCCCAGCAC[-/T]TTTTTGGGGCCAAGG | 9870 |
rs774637682 | snp | C/T | | | downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661202 | AAATCTTTTCCTTCC[C/T]CACCTTCCAGTCAAG | 9870 |
rs774650439 | snp | C/T | 5.70402e-05 | 0.00534012 | intron-variant | AREL1 | GRCh38.p7 | 14:74674144 | AGGAAATGAAGTGAA[C/T]GATAAATAAAAAGGC | 9870 |
rs774670383 | snp | C/G | 1.71164e-05 | 0.00292539 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670106 | GCGCAGATGAGCGGG[C/G]CGATTAGGGTTGGGA | 9870 |
rs774671450 | snp | C/T | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676605 | ATGGACAAGGTGTAA[C/T]TGTGCTCATCTCTCA | 9870 |
rs774698076 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673783 | AACTTAGTCTTGAAG[A/G]CAAAGGATCACTGTT | 9870 |
rs774805419 | snp | C/T | 1.66217e-05 | 0.0028828 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667325 | ATCACTTACCTCAAG[C/T]TCATTCTCATCAAAA | 9870 |
rs774822585 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683381 | ACGCCCAGCCTTGCG[C/T]ACAGTGAAGGCCACT | 9870 |
rs774824544 | snp | C/T | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713168 | TTGCGCCGTTGGTGA[C/T]TACGGAAGAACCAGG | 9870 |
rs774828492 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711135 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATCGCTTA | 9870 |
rs774864454 | in-del | -/ATAT | 1.67781e-05 | 0.00289634 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713580 | ATCAACTGCCCAGGG[-/ATAT]ATATTCTAATAAGAG | 9870 |
rs774894048 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687013 | TCATCTCAAAAATCT[C/G]CTACGATCTCTCAAA | 9870 |
rs774912033 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665596 | TTTCCTTTTTCTTAG[G/T]ATGCATTCTTTTGTG | 9870 |
rs774915958 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667263 | ACACCAAGCTGGTTC[C/T]TGTAAGCTACAAAAA | 9870 |
rs774938826 | snp | A/G | 9.93591e-05 | 0.00704767 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675786 | GTCTTCATCTTCCTC[A/G]TCAACAGCAGTGGAT | 9870 |
rs774952092 | snp | C/T | 7.18056e-05 | 0.00599146 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713460 | GTGTTTCCAACTTTT[C/T]TAATTCTAAAATTTC | 9870 |
rs774980956 | snp | A/G | 1.73024e-05 | 0.00294124 | intron-variant | AREL1 | GRCh38.p7 | 14:74674022 | GTGAACCAGATGTAA[A/G]GTTCAGCTTACTTTT | 9870 |
rs775034342 | snp | A/G | 1.66081e-05 | 0.00288163 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683530 | GCCCGTTCTTATAGA[A/G]TAACTGCCATGGGGA | 9870 |
rs775043679 | in-del | -/GTGTGTGTGTGTGAGA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699365 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGAGA]GAGAGAGAGAGAGAG | 9870 |
rs775067294 | snp | C/T | 0.000150089 | 0.00866152 | intron-variant | AREL1 | GRCh38.p7 | 14:74684431 | AAACCCCAATGGGTA[C/T]GGAGACAGAAACATT | 9870 |
rs775097537 | snp | C/G | 1.65954e-05 | 0.00288053 | intron-variant | AREL1 | GRCh38.p7 | 14:74667452 | TCAAGGCCAAGAACA[C/G]ACAGGATCCCACCTT | 9870 |
rs775112089 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679382 | AGCCATGACTATGCT[A/C]CTGCACGCCATCATG | 9870 |
rs775114311 | in-del | -/ATTT | 3.51401e-05 | 0.00419152 | intron-variant | AREL1 | GRCh38.p7 | 14:74676778 | ACAATGGAATCTAAC[-/ATTT]ATTTATTTATTTTAT | 9870 |
rs775136277 | snp | C/T | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712735 | TATCGGCTAGGAAAA[C/T]CAAATAGGAACCACA | 9870 |
rs775146483 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685988 | ACAGTTTCCCTCCCT[C/T]ATGCAAAGTGGTGCT | 9870 |
rs775146556 | snp | C/G | 1.65726e-05 | 0.00287855 | stop-gained, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684535 | AGACCGGGGATCCAG[C/G]TAATTTCCCCGCACG | 9870 |
rs775359237 | snp | G/T | 1.64738e-05 | 0.00286995 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713192 | AACCAGGAGTTTGGC[G/T]TGACCATGGTGAGAG | 9870 |
rs775375955 | in-del | -/AT | 1.66054e-05 | 0.00288139 | frameshift-variant, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670043 | TCCTAGAGAGGACTC[-/AT]AGAGACACTTGCCCA | 9870 |
rs775393764 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684339 | GCAATTCACTAGTTC[C/T]TGGAGGGAGTTGAAA | 9870 |
rs775405973 | snp | C/G | 1.67077e-05 | 0.00289026 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676321 | CTTCTTGAGGGCCGA[C/G]CTATAGGAAGGCAAC | 9870 |
rs775405989 | snp | C/T | 1.66416e-05 | 0.00288453 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74685655 | AGCCGAGGATCACAG[C/T]TGCAGCTGTTAAAAG | 9870 |
rs775410116 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671084 | GGAAAAGCCCCCTAG[C/T]ATGGAAACACCAGAG | 9870 |
rs775417448 | snp | C/T | 3.20436e-05 | 0.00400259 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714986 | CTTTAAAACCATAGA[C/T]CTCTTAGAAATCCAG | 9870 |
rs775425963 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695398 | ACTTTTATTTCTATT[C/T]ACTATGATGTTAGCA | 9870 |
rs775487442 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704906 | AAGAGAAAATCCTCT[C/T]GTCAAATTTTTTAAC | 9870 |
rs775519622 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695846 | CCCAGGTGAGTCCTA[C/T]GTATGCTGAAGTTTG | 9870 |
rs775535171 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679482 | AGACCATATGTTTAA[A/C]AAAGGACTAGCATAT | 9870 |
rs775630852 | snp | C/T | 1.66056e-05 | 0.00288141 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670028 | CTGCTTGTAGGCTCC[C/T]CCTAGAGAGGACTCA | 9870 |
rs775638644 | snp | C/G | 1.65987e-05 | 0.00288082 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676593 | CTTACCTCATGAATG[C/G]ACAAGGTGTAATTGT | 9870 |
rs775755649 | snp | C/T | 1.7159e-05 | 0.00292903 | intron-variant | AREL1 | GRCh38.p7 | 14:74669941 | AATGCACACCCAAGA[C/T]GTTACCTTGTAATGC | 9870 |
rs775789295 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707551 | CTGTAATCCCAGCAC[C/T]TTGGGAGGCCCAGGC | 9870 |
rs775816732 | snp | A/T | 8.33271e-05 | 0.00645419 | intron-variant | AREL1 | GRCh38.p7 | 14:74685567 | AGCAACCTTTACAAA[A/T]ATATAATAGAGAGAG | 9870 |
rs775818013 | snp | C/T | 1.65603e-05 | 0.00287747 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683374 | TTTCATAACGCCCAG[C/T]CTTGCGCACAGTGAA | 9870 |
rs775897127 | snp | A/G | 2.1841e-05 | 0.00330454 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713062 | TCTCCACCCGGCCTG[A/G]GAACCGGCTCGGGGG | 9870 |
rs775909255 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702379 | ACAGGCTCAACATCA[C/T]GTGTAAGCTGCCAAG | 9870 |
rs775909332 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677069 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 9870 |
rs775922612 | snp | C/T | 1.65359e-05 | 0.00287536 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713107 | AAGGAGTTTCCGCTT[C/T]CGGGCTATCCTTTGC | 9870 |
rs775944511 | snp | A/G | 1.71965e-05 | 0.00293222 | intron-variant | AREL1 | GRCh38.p7 | 14:74670877 | CAGTCCAGAGCTGAA[A/G]AGCATAATGAAAATA | 9870 |
rs776001451 | snp | A/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711608 | TGCCACACATCCTCA[A/G]GTTGGAAGACACACA | 9870 |
rs776007474 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687226 | ACAGATTTGTGGTCT[C/T]CTTAGAGGAATAAAA | 9870 |
rs776020904 | snp | C/T | 2.27384e-05 | 0.00337175 | intron-variant | AREL1 | GRCh38.p7 | 14:74664095 | AGGGAGAGCACAAGG[C/T]TGGGATCACACACAG | 9870 |
rs776068006 | in-del | -/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661726 | TGTTTAACAAAGACT[-/G]GTGCCTAAGGACCAC | 9870 |
rs776089013 | snp | G/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714157 | TGATCTTCACTGAGT[G/T]TAAGAGTCTCAGAAA | 9870 |
rs776124428 | snp | A/G | 1.73987e-05 | 0.00294942 | intron-variant | AREL1 | GRCh38.p7 | 14:74683268 | AGGGAAGGAGACAAA[A/G]GGAAAAAGAAAGGAA | 9870 |
rs776145944 | snp | A/C | 1.68286e-05 | 0.0029007 | intron-variant | AREL1 | GRCh38.p7 | 14:74671487 | GGCTTTCAGAGACTG[A/C]AAAGAAGTGAAAGGA | 9870 |
rs776161528 | snp | A/G | 1.6473e-05 | 0.00286988 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713175 | GTTGGTGATTACGGA[A/G]GAACCAGGAGTTTGG | 9870 |
rs776179325 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74701388 | GGCCTCACAAATCAC[A/G]GTGGAAGGTGAAAGG | 9870 |
rs776186802 | snp | A/G | 1.6566e-05 | 0.00287797 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672838 | TTACCTACCGATTCC[A/G]ACAAGGCATGTCTGC | 9870 |
rs776199875 | snp | C/T | 1.64746e-05 | 0.00287002 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713134 | TTGCCGGAAGCAGTA[C/T]GTGAATGACGTAGAA | 9870 |
rs776253700 | snp | A/G | 1.6591e-05 | 0.00288015 | intron-variant | AREL1 | GRCh38.p7 | 14:74667446 | TTAACTTCAAGGCCA[A/G]GAACAGACAGGATCC | 9870 |
rs776285751 | in-del | -/AAG | 0.000187952 | 0.00969231 | intron-variant | AREL1 | GRCh38.p7 | 14:74678152 | AAAACAATTTTGAAA[-/AAG]AAGAATAAAGTGGAG | 9870 |
rs776323663 | snp | A/T | 3.45393e-05 | 0.00415554 | intron-variant | AREL1 | GRCh38.p7 | 14:74669918 | AATGGCCAGGGGCCT[A/T]AGTAGGAAATGCACA | 9870 |
rs776325534 | in-del | -/A | 0.000127089 | 0.00797047 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74712982 | CTCCGCTGTCCTGGG[-/A]AGGGGCGGCAGCACT | 9870 |
rs776382125 | snp | C/G | 1.6585e-05 | 0.00287962 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683512 | GATGTGCAGGGAAAG[C/G]CTGCCCGTTCTTATA | 9870 |
rs776410790 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679785 | GTGAGCTGAGATTGT[A/G]CCATTGCACTCTAGC | 9870 |
rs776480679 | snp | A/C | 1.65633e-05 | 0.00287774 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663689 | AGAAGCTCCAGAGAG[A/C]ATGGGAGCCAACTGG | 9870 |
rs776508866 | snp | C/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662450 | AATGAGATTTTGAAT[C/G]TTGAAATTATTTTCA | 9870 |
rs776546374 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672335 | AGACATATGTAAAGA[C/G]AGAAATTTAGGTTTC | 9870 |
rs776565734 | snp | C/T | 1.66527e-05 | 0.00288549 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676307 | ACCAGTACTCTCTTC[C/T]TCTTGAGGGCCGAGC | 9870 |
rs776607245 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74678371 | AGCACGGTGGTGCAC[A/G]CCTGTAGTCCCAGCT | 9870 |
rs776626350 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685917 | CCACTTGCTTTATTG[C/T]TAATTTCAAAATGCA | 9870 |
rs776777301 | snp | A/T | 7.14681e-05 | 0.00597737 | intron-variant | AREL1 | GRCh38.p7 | 14:74673992 | GAGATAGTCCAGAGA[A/T]GAAGCATGCTTGATG | 9870 |
rs776844982 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697820 | ACATACTACTCTTGA[C/G]CAGGCAATCCCCCAA | 9870 |
rs776919174 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697175 | ACACACACACACACA[A/C]AGCCATGAAAAACAT | 9870 |
rs776944706 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74684415 | AAAGCAAGTTACTCA[A/G]AAACCCCAATGGGTA | 9870 |
rs777007582 | snp | G/T | 1.68505e-05 | 0.00290258 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713596 | ATATTCTAATAAGAG[G/T]CTAGAGAGGATAAGT | 9870 |
rs777077719 | snp | A/G | 1.71596e-05 | 0.00292908 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675918 | GCCTGAAGTGGACAC[A/G]TTGCGTTCGACGATA | 9870 |
rs777084148 | snp | C/T | 1.65891e-05 | 0.00287998 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676751 | AGAAGGAACCACCAT[C/T]CCTGGAACAAAGACA | 9870 |
rs777106008 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74709451 | ATTTCAACTCCCACA[A/T]CTCTATTCAGCCACC | 9870 |
rs777125532 | snp | A/C | 1.66724e-05 | 0.0028872 | intron-variant | AREL1 | GRCh38.p7 | 14:74685557 | AAAGGACCCAAGCAA[A/C]CTTTACAAAAATATA | 9870 |
rs777159161 | snp | C/T | 1.74528e-05 | 0.00295399 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670126 | TAGGGTTGGGATGCA[C/T]CTGTCCAAGAAAGAG | 9870 |
rs777182135 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675207 | AGGCTAGATTTTTAA[A/G]TGAAGAATGGTACAC | 9870 |
rs777204298 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662617 | GGAGTACAGGGGTTG[A/G]CAGGTGTTTACTGTG | 9870 |
rs777208686 | snp | C/T | 0.000536481 | 0.0163693 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713012 | TCAGCAGAAGACGGG[C/T]TCCCCACTCTCCCAC | 9870 |
rs777255147 | in-del | -/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664449 | TCTTCTTTTCCTTTC[-/T]TTTTTTTTTTTTTTT | 9870 |
rs777263416 | snp | C/T | 4.02463e-05 | 0.0044857 | missense | AREL1 | GRCh38.p7 | 14:74664074 | AAAACCACCTCATGA[C/T]CTGGCAGGGAGAGCA | 9870 |
rs777291202 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682753 | AGTTCATGCAAGATC[C/T]GTTTGTTTAGAAAAG | 9870 |
rs777318394 | snp | C/T | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670775 | ACTAATGCTTGGTTG[C/T]TGTCACTGAACCGGG | 9870 |
rs777349727 | snp | A/C | 0.00695144 | 0.058544 | intron-variant | AREL1 | GRCh38.p7 | 14:74676372 | GTATTTTCCCATTTA[A/C]AAGCCACTTTACTCC | 9870 |
rs777354060 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665119 | CAATAGTTGCTAACC[A/G]GTGGGTAAAAAAAAG | 9870 |
rs777354130 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697402 | ATTCAATTTTCAAAA[A/G]GTGCACAGGTTAGGG | 9870 |
rs777366195 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670629 | CAATCTGATTAGCTT[A/T]TATTTTAAGCAGTAA | 9870 |
rs777367895 | snp | C/T | 3.31175e-05 | 0.00406911 | missense | AREL1 | GRCh38.p7 | 14:74663773 | CCAGCTGCAGCATCC[C/T]GTGCACCTCTTCATA | 9870 |
rs777388158 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703629 | TTTCACTTAGCATAA[A/T]GGTTCTTAGATTCAT | 9870 |
rs777391393 | snp | A/C | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662937 | CAGTAGTCTCCAAGC[A/C]AGCCATATGCCTAGG | 9870 |
rs777418689 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710868 | TGCGATTGAGCATCC[C/T]AGGACCTGAAAACTT | 9870 |
rs777468006 | snp | C/T | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676270 | TCTGCCTGTTGGATG[C/T]TACTGATTTCTCAAA | 9870 |
rs777481467 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697585 | ATATTTATACAGTTG[C/T]CTATTTCTGCTATTG | 9870 |
rs777502460 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663004 | TCATATTCTTCAGTC[C/T]ATCTGCTTTTCTCAC | 9870 |
rs777638638 | snp | G/T | 5.00889e-05 | 0.00500419 | intron-variant | AREL1 | GRCh38.p7 | 14:74664962 | TTACTATGACAGTCA[G/T]AGAGACAAAGACCCA | 9870 |
rs777647215 | snp | A/C | 3.31312e-05 | 0.00406995 | missense, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683331 | TAGGGACTATATGCC[A/C]CATTTAATCCACCAA | 9870 |
rs777759514 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674877 | TCTGCCAGGGAAGGG[A/T]GGCAAGATGGGGTGA | 9870 |
rs777778000 | snp | C/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662098 | GCATGGAGGATCCTG[C/G]GGTATAGAGACCCTG | 9870 |
rs777810408 | snp | C/T | 1.69864e-05 | 0.00291426 | intron-variant | AREL1 | GRCh38.p7 | 14:74673264 | TAAAACCCTCAAGGC[C/T]AGTAAAAGTCCTCCA | 9870 |
rs777855034 | snp | A/G | 1.65677e-05 | 0.00287812 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664863 | ATGCCATGAGCCACC[A/G]ACAACTACTGCATGG | 9870 |
rs777862454 | in-del | -/A | 1.67336e-05 | 0.00289249 | intron-variant | AREL1 | GRCh38.p7 | 14:74676327 | AGGGCCGAGCTATAG[-/A]GAAGGCAACAGAGCA | 9870 |
rs777906007 | snp | A/G | 1.68684e-05 | 0.00290412 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713092 | GATTGCCCTTTCCCC[A/G]AGGAGTTTCCGCTTC | 9870 |
rs777940769 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668296 | ACAGCTTAAAACCAT[C/T]ATCCAGGAATATTTG | 9870 |
rs777942518 | snp | A/G | 1.6715e-05 | 0.00289089 | intron-variant | AREL1 | GRCh38.p7 | 14:74670755 | CACCCACCCGTCACC[A/G]ACTCACTAATGCTTG | 9870 |
rs777967736 | snp | C/T | 1.66679e-05 | 0.00288681 | upstream-variant-2KB, missense, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713530 | ACCATGAAGCGAATG[C/T]TTAGTCTCAGAGATC | 9870 |
rs778006610 | snp | A/G | 1.65963e-05 | 0.0028806 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673096 | GTTCTTATGCAGGGA[A/G]CGGATAAAAGTGGCT | 9870 |
rs778027348 | snp | A/C | 2.4797e-05 | 0.00352106 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713054 | AGAGTTGGTCTCCAC[A/C]CGGCCTGGGAACCGG | 9870 |
rs778044975 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688124 | TCTGCCTCCCGGGTT[C/T]GCGCCATTCTCCTGC | 9870 |
rs778059748 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667141 | TTTGCTACTAATTTT[C/T]ACATTCTAATTTTTT | 9870 |
rs778063754 | snp | C/G/T | 6.71325e-05 | 0.00579331 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669623 | CTGGAGAACATAGGA[C/G/T]CCAGAGGCTTTGTCC | 9870 |
rs778115322 | snp | C/T | 3.33189e-05 | 0.00408146 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74667520 | CAGCCGATATTGGGC[C/T]AGCAAATTTAAATAG | 9870 |
rs778133017 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700864 | ACAACAACAAAAAGA[G/T]GTTTTTTAACCGAGA | 9870 |
rs778142034 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693501 | ATGAGAAGAGACTAC[G/T]AATTAGTAAATGAAG | 9870 |
rs778167707 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74702049 | GGGTACAGCCTCCTC[C/G]CCAGCTGCTTTCGTG | 9870 |
rs778247006 | snp | C/T | 0.000116845 | 0.00764256 | upstream-variant-2KB, utr-variant-5-prime, missense | AREL1, FCF1 | GRCh38.p7 | 14:74713516 | CAAGGAAGTATGCGA[C/T]CATGAAGCGAATGCT | 9870 |
rs778267085 | snp | C/T | 7.70347e-05 | 0.00620576 | upstream-variant-2KB, missense, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714918 | AAAGAAAAGAAGGAT[C/T]CCAGCGCATTAAAGG | 9870 |
rs778287897 | snp | A/G | 6.63702e-05 | 0.00576027 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684601 | GTCCTCATTCTGGAG[A/G]AAGCTGACTACACGT | 9870 |
rs778340370 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705490 | CTCTGCACCCCTGAT[A/C]CTGGTTCTTAAAACA | 9870 |
rs778359450 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694427 | AGGAACAAAACTGTT[C/T]ATGTAGCACAAGTCC | 9870 |
rs778388327 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687276 | TTGAGTCATGAGGGC[C/T]AGAAAAATTCCCACC | 9870 |
rs778437737 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690303 | TCCAAAGAAACCAAC[A/G]TAATTGCATATAGTA | 9870 |
rs778490827 | snp | C/T | 1.65745e-05 | 0.00287871 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684524 | GAGACTTTGCAAGAC[C/T]GGGGATCCAGGTAAT | 9870 |
rs778531929 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74685440 | TGCTCAATAAACCCA[A/G]ATGAATGAATTCCAA | 9870 |
rs778564273 | in-del | -/AC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697157 | TCCTGTCACACATAC[-/AC]ACACACACACACACA | 9870 |
rs778591571 | snp | A/G | 3.32265e-05 | 0.0040758 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684619 | GCTGACTACACGTGC[A/G]GCAAGCTCAAAGAGG | 9870 |
rs778594901 | snp | A/G | 1.65754e-05 | 0.00287879 | synonymous-codon, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669673 | TTGACCTGATTTATT[A/G]TATTTCTCTTCTGCA | 9870 |
rs778627218 | snp | C/T | 0.000163279 | 0.00903397 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661365 | GGGCTTGGTCTCTGC[C/T]AATTTTCCAGAAACA | 9870 |
rs778634161 | snp | C/T | 8.30186e-05 | 0.00644223 | intron-variant | AREL1 | GRCh38.p7 | 14:74664828 | TGAAAGAAGTTTGGT[C/T]CATTTACCTTTTCTC | 9870 |
rs778641332 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74672202 | TTACACCTGCCCTAC[A/G]TGGGAGTTCCAAGGG | 9870 |
rs778655379 | snp | A/G | 1.65899e-05 | 0.00288005 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683315 | TTGAAAAATTTTGTA[A/G]TAGGGACTATATGCC | 9870 |
rs778661857 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704694 | TTTGCAAATATTTTC[C/T]GTGGCTTGCCTCTTC | 9870 |
rs778679369 | snp | C/T | 1.68855e-05 | 0.00290559 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664027 | AAGTAGCCGAGCCAA[C/T]TCCTCCTGGGTCAGA | 9870 |
rs778688142 | in-del | -/AAAAT | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711544 | GGAGGCTCTGTCTCA[-/AAAAT]AAAATAAAATAAAAT | 9870 |
rs778707370 | snp | C/T | 1.66944e-05 | 0.0028891 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74669990 | TGGGCCAGGAAAGAG[C/T]GGGTGAAGCGAGCTC | 9870 |
rs778745727 | snp | C/T | 2.77058e-05 | 0.00372185 | | | GRCh38.p7 | 14:74713047 | AGACCCCAGAGTTGG[C/T]CTCCACCCGGCCTGG | 9870 |
rs778754189 | snp | A/G | 0.00013299 | 0.00815336 | | | GRCh38.p7 | 14:74669805 | GACACAGAACAGAAC[A/G]TGAATACTCTTGCCC | 9870 |
rs778760744 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710583 | TATTGTCTAATCACC[A/G]AGAGATACATCAAAA | 9870 |
rs778776223 | snp | A/G | 1.66062e-05 | 0.00288146 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670842 | AGATTAGCTCAAACC[A/G]TTCCCGGCGAGGCCC | 9870 |
rs778846797 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697648 | ACTTTCTTCATCAGT[C/T]AGCCTCTCCAGTCTC | 9870 |
rs778932290 | snp | C/G | 0.000299401 | 0.0122316 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74673113 | GGATAAAAGTGGCTG[C/G]TAGAATGTTCCTCTC | 9870 |
rs778960599 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663035 | TGGCTACAATTCAAG[A/G]AAAAGCTTACAGAGT | 9870 |
rs778976429 | snp | C/T | 0.000368664 | 0.0135719 | intron-variant | AREL1 | GRCh38.p7 | 14:74678325 | AACATAGTGAGACCC[C/T]ATTCCTACAAAAAAG | 9870 |
rs778992669 | snp | A/T | 1.72785e-05 | 0.00293921 | intron-variant | AREL1 | GRCh38.p7 | 14:74670737 | AACATAATCCACATT[A/T]TCCACCCACCCGTCA | 9870 |
rs779000733 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703412 | CACTGGATCCCTCCC[A/G]CAACAATGGGAATTA | 9870 |
rs779048821 | snp | C/T | 3.3117e-05 | 0.00406908 | synonymous-codon | AREL1 | GRCh38.p7 | 14:74663780 | CAGCATCCTGTGCAC[C/T]TCTTCATAGGAGTCA | 9870 |
rs779068832 | snp | A/G | 1.65644e-05 | 0.00287783 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675756 | CTTCTCAGGGGTGTG[A/G]CACTCAGAGGGCGAG | 9870 |
rs779113483 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74687169 | GGTCCTCAGGGAAGT[C/T]ACAGCACTCAGCAAA | 9870 |
rs779201523 | in-del | -/TTTTATTTTTAT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688824 | TCAAAAGCCCTTCTA[-/TTTTATTTTTAT]TTTTATTTTTATTTT | 9870 |
rs779280709 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712081 | AAGAAAAAAAAAGAA[-/AG]AAAGAAAGAAAGAAA | 9870 |
rs779281659 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674918 | AATATGTTGGTGGTA[C/T]AGGGGAAGGTCCTCA | 9870 |
rs779282948 | snp | A/T | 1.65737e-05 | 0.00287864 | intron-variant | AREL1 | GRCh38.p7 | 14:74672825 | CAGAGATGAAATTTT[A/T]CCTACCGATTCCAAC | 9870 |
rs779283154 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74681042 | AATCAAAAAATTAAC[C/T]GAGCGTGGTGGTGCA | 9870 |
rs779338108 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713967 | GCCTGGTACTCAAAT[A/G]TTTTTGTCAGAGAAA | 9870 |
rs779340629 | snp | A/T | 1.65748e-05 | 0.00287874 | intron-variant | AREL1 | GRCh38.p7 | 14:74667413 | TAAAGTCATACCCAC[A/T]CCATGGATACAGGTA | 9870 |
rs779449779 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672894 | TGGTCTTTTCATATG[C/T]ACCTGCCGAAGCTCT | 9870 |
rs779451406 | snp | G/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672913 | TGCCGAAGCTCTCGC[G/T]GGAAAAAGTTCACCT | 9870 |
rs779473371 | snp | C/G | 0.000567864 | 0.0168407 | missense | AREL1 | GRCh38.p7 | 14:74667503 | TCTTTCACTTGACTG[C/G]CCAGCCGATATTGGG | 9870 |
rs779477618 | in-del | -/TA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695874 | TTGAGAAACATGGTT[-/TA]GACTCTAGAGCAATC | 9870 |
rs779489499 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682484 | AATTCGACCACCAAC[C/T]GATGAAAGGATAAAT | 9870 |
rs779493399 | snp | A/T | 5.04147e-05 | 0.00502044 | intron-variant | AREL1 | GRCh38.p7 | 14:74683581 | AAGCAGAGGAAAAAA[A/T]CATTTCCTGTGTAGA | 9870 |
rs779619603 | snp | A/G | 0.000116462 | 0.00763003 | upstream-variant-2KB, missense, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714876 | TTTCTTCCTAGTAAA[A/G]AAAAGGATAGATTAA | 9870 |
rs779620091 | snp | G/T | 1.64751e-05 | 0.00287007 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713241 | ACGTTATCAGGCCAC[G/T]TTTTGGGTGGAGAAG | 9870 |
rs779652469 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673470 | CTTCTAACATAAAAT[A/G]TAAGAAGGGTGATAT | 9870 |
rs779728880 | snp | G/T | 0.000187741 | 0.00968685 | intron-variant | AREL1 | GRCh38.p7 | 14:74678229 | AGGCTGTGTGACTTG[G/T]CTCACGCCTGTAATC | 9870 |
rs779751396 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694761 | TTGGGAGGCTGAAGC[A/G]GGCGGATCATGAGGT | 9870 |
rs779777107 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74686615 | ATTACGTAGAGACAA[A/G]ACAGCTAAAAATTTC | 9870 |
rs779854887 | snp | A/C | 1.69172e-05 | 0.00290832 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670094 | ATACATTTTCAGGCG[A/C]AGATGAGCGGGGCGA | 9870 |
rs779876162 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693575 | ACACATAAACTCACA[A/G]ATACAATTATCCCTA | 9870 |
rs779925748 | snp | A/G | 3.31318e-05 | 0.00406999 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675848 | GTGGCAGGTGCCATG[A/G]AGTGCTGCTACAGTT | 9870 |
rs779981383 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74714021 | CATTTTATAAGTCTT[A/G]CTAATATAAGAATCC | 9870 |
rs780037820 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699310 | ACTTCAAAGTTAACT[A/G]GCATGTCTAAAGTGT | 9870 |
rs780067948 | snp | C/G | 5.8682e-05 | 0.00541642 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713042 | CCAACAGACCCCAGA[C/G]TTGGTCTCCACCCGG | 9870 |
rs780068047 | snp | A/C | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676714 | ATACAAGAGTAGAAA[A/C]GTGGCACACAATTTT | 9870 |
rs780090234 | snp | C/T | 1.65586e-05 | 0.00287733 | intron-variant | AREL1 | GRCh38.p7 | 14:74663892 | CATCAGGCGGGCAGA[C/T]ACCTACCATGTGTGT | 9870 |
rs780094326 | in-del | -/G | 0.000186829 | 0.0096633 | intron-variant | AREL1 | GRCh38.p7 | 14:74698873 | AAAAAAAAAAAAAAA[-/G]AAAAGCTGGGTGTGG | 9870 |
rs780125146 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691613 | GAATGCAATGCCAAT[C/T]CTCTAGTGCAGAAAT | 9870 |
rs780146613 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682095 | TGGTGGCAAAGAGGT[A/G]GGTGATGATAATTCA | 9870 |
rs780157590 | snp | A/G | 1.65616e-05 | 0.00287759 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683474 | CTCGACATGAGAGAT[A/G]TGAACTCTTAGTCCC | 9870 |
rs780172353 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74710623 | CTATTAGCTCTACAC[A/G]TGAATGGCAGCTTGA | 9870 |
rs780183895 | snp | A/T | 1.65729e-05 | 0.00287857 | intron-variant | AREL1 | GRCh38.p7 | 14:74667407 | GCAAGTTAAAGTCAT[A/T]CCCACACCATGGATA | 9870 |
rs780191794 | snp | A/G | 1.65754e-05 | 0.00287879 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675730 | CAGTACACCTTCTTC[A/G]GTTTCTTCACCTTCT | 9870 |
rs780204025 | snp | C/T | 1.66754e-05 | 0.00288746 | intron-variant | AREL1 | GRCh38.p7 | 14:74683561 | GAAGAAGGACACCTG[C/T]TAGCAAGCAGAGGAA | 9870 |
rs780256663 | snp | C/T | 1.64749e-05 | 0.00287005 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713233 | AAGAAGGGACGTTAT[C/T]AGGCCACTTTTTGGG | 9870 |
rs780320998 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74675958 | TCCTCTGAAGTATAA[C/T]AAGGAATAAGGTTTA | 9870 |
rs780436170 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704327 | GAGGTCCTGACGACA[C/T]GTGCCCAAGGTGGTT | 9870 |
rs780461726 | snp | C/T | 3.32878e-05 | 0.00407956 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74671417 | ACTGACCTTCTTCAT[C/T]CTGGAAAACAACCTC | 9870 |
rs780520218 | in-del | -/C | 1.65784e-05 | 0.00287905 | intron-variant | AREL1 | GRCh38.p7 | 14:74673041 | GGATGTGGCTGGGCT[-/C]ACTACCTTCCCTATA | 9870 |
rs780533710 | snp | C/T | | | synonymous-codon | AREL1 | GRCh38.p7 | 14:74664009 | GGAGCCTGTTGTGAA[C/T]TGAAGTAGCCGAGCC | 9870 |
rs780560694 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703562 | CATTCAAAAGGTACA[C/T]AGAAATACATTTGTA | 9870 |
rs780566531 | snp | C/T | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, utr-variant-5-prime | AREL1, FCF1 | GRCh38.p7 | 14:74713159 | GTAGAAGTATTGCGC[C/T]GTTGGTGATTACGGA | 9870 |
rs780572133 | snp | C/T | 1.656e-05 | 0.00287745 | intron-variant | AREL1 | GRCh38.p7 | 14:74663866 | TCATACCACCAAAAA[C/T]ACTGGGCATGCATCA | 9870 |
rs780578876 | snp | A/G | 5.15974e-05 | 0.00507898 | intron-variant | AREL1 | GRCh38.p7 | 14:74676367 | ATATAGTATTTTCCC[A/G]TTTACAAGCCACTTT | 9870 |
rs780594281 | snp | G/T | 1.6821e-05 | 0.00290004 | intron-variant | AREL1 | GRCh38.p7 | 14:74676560 | TCTCTCTAGCACACA[G/T]ATAAAGAAGGGAGAC | 9870 |
rs780724454 | in-del | -/TGTT | | | intron-variant | AREL1 | GRCh38.p7 | 14:74668805 | ATTATCATTTGATGC[-/TGTT]TAACACCACAATGTA | 9870 |
rs780767827 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670455 | GACAAAGATCTAGTA[C/G]AGGAATCATTTGCTT | 9870 |
rs780802289 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682613 | TGTACCCTCCAAATC[A/G]CATGTTGAAATGTGA | 9870 |
rs780812919 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674512 | GAGGCTGAGGCACAA[A/G]AATCGCTTGAACCCG | 9870 |
rs780885128 | snp | C/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74672908 | GTACCTGCCGAAGCT[C/G]TCGCTGGAAAAAGTT | 9870 |
rs780896838 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74707142 | GGAGGCCGAGGCGGG[C/T]AGATCACCTGAGGTC | 9870 |
rs780978467 | snp | A/G | 1.66646e-05 | 0.00288652 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670071 | CCCACGAGCCGTCCC[A/G]CAAACTCATACATTT | 9870 |
rs780997962 | snp | A/G | 5.0618e-05 | 0.00503055 | synonymous-codon, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74674088 | GGGGATGATCTTCAG[A/G]TAGAACTCCTTCACT | 9870 |
rs781002960 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696446 | TGATCAAGGCTAATA[C/T]TTCCTAAAACTAGTA | 9870 |
rs781111595 | in-del | -/G | 8.27965e-05 | 0.00643362 | intron-variant | AREL1 | GRCh38.p7 | 14:74663885 | GGGCATGCATCAGGC[-/G]GGCAGATACCTACCA | 9870 |
rs781145383 | snp | C/T | 1.66286e-05 | 0.0028834 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74675712 | ACCTTTGGTGACACA[C/T]AGCAGTACACCTTCT | 9870 |
rs781159476 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74705821 | TTTCTTTTTGTATAG[A/T]ATACACAAAGGCATA | 9870 |
rs781184364 | snp | C/T | 1.65594e-05 | 0.0028774 | missense | AREL1 | GRCh38.p7 | 14:74663785 | TCCTGTGCACCTCTT[C/T]ATAGGAGTCATATGT | 9870 |
rs781198013 | in-del | -/GTGAGA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699375 | TGTGTGTGTGTGTGT[-/GTGAGA]GAGAGAGAGAGAGAG | 9870 |
rs781206568 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74673603 | TATTTTTATAAAATG[A/G]CACATTCTAGCCTTT | 9870 |
rs781239421 | snp | C/T | 1.66106e-05 | 0.00288184 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670014 | CGAGCTCGGACCAAC[C/T]GCTTGTAGGCTCCTC | 9870 |
rs781290548 | snp | A/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699667 | ACCAGAAATATGCCA[A/T]AGGAACTTAATTCTT | 9870 |
rs781329354 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74666648 | CTGAAAAAATAAATT[A/C]TATTACTCCCTTAAA | 9870 |
rs781336835 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683450 | GGTCACTGGAATTTC[C/T]ACTGCTAGCTCGACA | 9870 |
rs781365393 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74679175 | GATTTCATCAAAATT[C/G]AAAACATGTGCTCTG | 9870 |
rs781378975 | in-del | -/ACAC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697155 | GATCCTGTCACACAT[-/ACAC]ACACACACACACACA | 9870 |
rs781412833 | snp | A/G | 1.66067e-05 | 0.00288151 | intron-variant | AREL1 | GRCh38.p7 | 14:74669780 | TTTCAAAGTACTGAG[A/G]AGGCAGAAAGACACA | 9870 |
rs781435728 | snp | A/G | 1.66117e-05 | 0.00288194 | missense, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74684617 | AAGCTGACTACACGT[A/G]CGGCAAGCTCAAAGA | 9870 |
rs781448737 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665073 | TAATGCCAGAATACT[A/G]CTTTAGGAAAATCAA | 9870 |
rs781450596 | snp | C/T | 1.67382e-05 | 0.00289289 | intron-variant | AREL1 | GRCh38.p7 | 14:74671403 | TATAAAATTTCAAAA[C/T]TGACCTTCTTCATCC | 9870 |
rs781458567 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74700667 | CGCCTGTATTCCCAG[A/C]TACTGGGGAAGCTGA | 9870 |
rs781463875 | snp | A/G | 3.31203e-05 | 0.00406928 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74683363 | CTTCACTGTGATTTC[A/G]TAACGCCCAGCCTTG | 9870 |
rs781482445 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74683610 | GAGTGAGTGGGGAGA[C/G]AGGAAGTAGCTGGCA | 9870 |
rs781490135 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677395 | CAGCTACTCAGGAAG[A/C]TAAGGCAAGAGGATC | 9870 |
rs781490197 | snp | A/C | 0.000164352 | 0.00906361 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661299 | ACAAAATATTTACAT[A/C]ATCAGCTGCAACTGC | 9870 |
rs781492355 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693153 | CCAGGTTACGGACAG[A/C]CTTATATGCCATGGT | 9870 |
rs781545144 | in-del | -/A | 5.74207e-05 | 0.00535789 | intron-variant | AREL1 | GRCh38.p7 | 14:74674146 | GAAATGAAGTGAATG[-/A]TAAATAAAAAGGCTC | 9870 |
rs781583288 | snp | A/G | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713390 | GTCTGGGTTATTTGA[A/G]GCAAGAAGGGAAGGC | 9870 |
rs781592753 | snp | A/C/T | 5.08706e-05 | 0.00504313 | intron-variant | AREL1 | GRCh38.p7 | 14:74676112 | ACGGCTGAAGAACAG[A/C/T]ACTAAATCATACTTT | 9870 |
rs781671171 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691772 | TACATATTCTAAAAT[C/T]CTCTGCTTTTTCGGA | 9870 |
rs781679907 | snp | C/T | 1.65663e-05 | 0.002878 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74676236 | GAATGCAGGGTGAGT[C/T]GCAAGAACACCTGGA | 9870 |
rs781753257 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74671928 | CGAGCCATGCCACAC[A/G]GAGAATATGGCTGAG | 9870 |
rs781754610 | snp | C/G/T | 3.58354e-05 | 0.00423281 | intron-variant | AREL1 | GRCh38.p7 | 14:74684707 | AGAGAACACACAAAC[C/G/T]GCCTGCCAGTTACAC | 9870 |
rs781761535 | snp | G/T | 1.67295e-05 | 0.00289214 | missense, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670864 | GCGAGGCCCTCCCCA[G/T]TCCAGAGCTGAAAAG | 9870 |
rs796078255 | snp | A/G | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662143 | ACCCCAAGGATGAGT[A/G]AGGTCAGCACCCATG | 9870 |
rs796291203 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74667285 | CTACAAAAATGCCAA[A/G]TTAAGAATGGGAGTC | 9870 |
rs796454085 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703822 | ACAAGTCTGTGTAGG[C/T]ACATGATTTCATTTC | 9870 |
rs796468869 | in-del | -/TC | | | intron-variant | AREL1 | GRCh38.p7 | 14:74689591 | ATCTTATAGCACTTT[-/TC]TTTTTTTTTTTTTTT | 9870 |
rs796480740 | in-del | -/AA | | | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661616 | ATTAGAAAAAAAAAA[-/AA]CAAAACAGTAAAAGA | 9870 |
rs796549641 | in-del | C/GAG | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699383 | GTGTGTGTGAGAGAG[C/GAG]GAGAGAGAGCAAGAG | 9870 |
rs796597875 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74670259 | GCCCATCCAAATGTT[A/G]GTTTTTTGGTAGCCA | 9870 |
rs796624194 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74682205 | GTCCAGAGCCTTACT[C/T]TGCTATCAGAGAAAG | 9870 |
rs796724634 | in-del | AA/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74674617 | AAAAAATAAAATAAA[AA/T]AAAAAAAATATGACT | 9870 |
rs796788060 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74704730 | CTTAACAGAAAATAC[A/G]CTTTTTAAAGAGTAC | 9870 |
rs796833373 | in-del | -/G | | | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74712086 | AAAAAAAGAAAGAAA[-/G]AAAGAAAGAAAAAGA | 9870 |
rs796868685 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74669844 | GTAACTGCTTAGAAC[C/T]ACTTATCCCTTCAAC | 9870 |
rs796936848 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74688437 | TTGTGGAGTCCTCGG[C/T]CATTTTTCCCCTGTC | 9870 |
rs796962770 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74677780 | TGCTGGAATTACAGG[C/T]GTAAGCCACGGTGCC | 9870 |
rs796990395 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74690399 | GGAATTTTCCAGATG[C/G]GATCTTCCTTGTAGA | 9870 |
rs796996799 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665270 | GTATTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 9870 |