SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9441 | snp | C/T | 0.423413 | 0.180077 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661722 | TCCTTAGGCACCAGT[C/T]TTTGTTAAACAAAAC | 9870 |
rs16661 | snp | A/C | 0.46137 | 0.133501 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661613 | AGGATTAGAAAAAAA[A/C]AAAACAAAACAGTAA | 9870 |
rs752857 | snp | C/T | 0.439085 | 0.163545 | intron-variant | AREL1 | GRCh38.p7 | 14:74664241 | GAATTTACACTGTCA[C/T]ATGATTAGGAGGGTA | 9870 |
rs1045430 | snp | A/C | 0.449726 | 0.150364 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663532 | TCCCTGCCCATATCT[A/C]CCACAGGCCACTTTG | 9870 |
rs1045436 | snp | C/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662114 | GTCCGGGATCCAGCA[C/T]CAGGGTCTCTATACC | 9870 |
rs1045437 | snp | G/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662111 | CGGGATCCAGCATCA[G/T]GGTCTCTATACCCCA | 9870 |
rs1045578 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661442 | GGGCCAGCTACCCTT[C/T]TGGCCTTTTAGCGTC | 9870 |
rs1045621 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74661375 | AGTGTCAGCATGTTT[C/T]TGGAAAATTGGCAGA | 9870 |
rs2080669 | snp | A/G | 1.67508e-05 | 0.00289398 | intron-variant, downstream-variant-500B | AREL1 | GRCh38.p7 | 14:74669627 | AGAACATAGGACCCA[A/G]AGGCTTTGTCCTCTT | 9870 |
rs2270424 | snp | A/G | 0.397744 | 0.201673 | utr-variant-5-prime, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74692304 | GTGCAGGGTGCAATC[A/G]ACTGCCAAAGGACGC | 9870 |
rs2270425 | snp | C/G | 0.481084 | 0.0953954 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713031 | CCACTCTCCCACCAA[C/G]AGACCCCAGAGTTGG | 9870 |
rs2287399 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | AREL1 | GRCh38.p7 | 14:74670297 | GTAATTCAAAGTGAC[C/T]AGAAGATAAAGGGCA | 9870 |
rs2302832 | snp | C/T | 0.450357 | 0.149522 | intron-variant | AREL1 | GRCh38.p7 | 14:74670961 | TTTATACTCTCCACA[C/T]TCCCTCTATTGTACT | 9870 |
rs2359142 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74689592 | TCTTATAGCACTTTT[C/T]TTTTTTTTTTTTTTT | 9870 |
rs2359143 | snp | A/G | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74701982 | ccaggtcacgctgac[A/G]caagaggtgggttcc | 9870 |
rs2884642 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664449 | TCTTCTTTTCCtttc[C/T]ttttttttttttttt | 9870 |
rs3080652 | in-del | -/TAAA | | | intron-variant | AREL1 | GRCh38.p7 | 14:74694199 | aaataaataaataaa[-/TAAA]taatGCCAACAGACT | 9870 |
rs3214407 | in-del | -/T | | | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713640 | ATTATTTTGTTTTTT[-/T]GCTTATTATCGTGTC | 9870 |
rs3759742 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | AREL1 | GRCh38.p7 | 14:74709121 | CTTTAGCTATTAACT[A/G]ACTTGGGTTTAAATT | 9870 |
rs3813557 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662286 | AGGACTTTGGCAATG[C/G]CTTGGCCTCCTGGAA | 9870 |
rs3813559 | snp | G/T | 0.0240643 | 0.107019 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661716 | GGCACCAGTCTTTGT[G/T]AAACAAAACCCTTTG | 9870 |
rs3834533 | in-del | -/C | 0.0287284 | 0.116357 | intron-variant | AREL1 | GRCh38.p7 | 14:74708662 | GCCAATAGTTAACAT[-/C]TGTTAATTGATTTTC | 9870 |
rs4899529 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74689215 | GTTCTGTAAGCATTT[C/T]CTGTAAGCATGTTCC | 9870 |
rs4899530 | snp | A/G | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74699122 | tactgaatgatctta[A/G]acaagttacagcagg | 9870 |
rs4899531 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74699378 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 9870 |
rs4899532 | snp | A/G | 0.375797 | 0.216044 | intron-variant | AREL1 | GRCh38.p7 | 14:74707429 | gcactttgggaggcc[A/G]aggtgggcggattac | 9870 |
rs5809676 | in-del | -/A | 0.375 | 0.216506 | intron-variant | AREL1 | GRCh38.p7 | 14:74690285 | AAAAAAAAAAAAAAA[-/A]GCTCCAAAGAAACCA | 9870 |
rs6574189 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74699790 | aggacttgctgTAAA[C/T]TTCTCTTCAGTTGCC | 9870 |
rs6574190 | snp | A/G | 0.397271 | 0.202018 | intron-variant | AREL1 | GRCh38.p7 | 14:74700312 | ACAGAAAGCTAAAAT[A/G]ACTTGCCTATAGCCA | 9870 |
rs7143215 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | AREL1 | GRCh38.p7 | 14:74683987 | TAATGCTACAGTGGA[A/G]AAGTCAATGcaggag | 9870 |
rs7144650 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | AREL1 | GRCh38.p7 | 14:74708403 | TTTGCACAGCCCACC[C/T]GGGATTTCTTCTTTA | 9870 |
rs7145575 | snp | A/T | 0.444133 | 0.157519 | intron-variant | AREL1 | GRCh38.p7 | 14:74678825 | agaacatcttcagga[A/T]ctgagaccaaagatt | 9870 |
rs7148840 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AREL1 | GRCh38.p7 | 14:74684784 | AAAGGAGGTCAGGAT[A/G]AGACTGTAAGACTGC | 9870 |
rs7149057 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74691647 | ACTTGCTTACGAAGG[A/T]TCCTGGTCTGGTTGC | 9870 |
rs7152804 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74697305 | AAAGAAAGACGTTTG[C/T]TTTGTAAGATGCAAT | 9870 |
rs7153812 | snp | A/G | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74706787 | CGTAGTTATACTTCC[A/G]TGTAGTAAAATCTAT | 9870 |
rs7155338 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AREL1 | GRCh38.p7 | 14:74701812 | gttactttctagata[C/T]aatgggagtacaggc | 9870 |
rs7156373 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74703431 | caatgggaattatgg[A/G]agctaaaattcaagg | 9870 |
rs7157439 | snp | A/G | 0.0599851 | 0.162463 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711231 | agcgaaactaactcc[A/G]tctcaaaaaaaaaaa | 9870 |
rs7160996 | snp | C/T | 0.459118 | 0.137002 | intron-variant | AREL1 | GRCh38.p7 | 14:74695281 | ggcagggtttcacca[C/T]gttggccaggctggt | 9870 |
rs7493409 | snp | A/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74670335 | ACATAATTAAGAATC[A/T]TATATTAAGTTTGTG | 9870 |
rs8004430 | snp | C/T | 0.393987 | 0.204372 | intron-variant | AREL1 | GRCh38.p7 | 14:74704980 | TTAAGTTTTATTCCC[C/T]TTGTTTCTTTCAAAT | 9870 |
rs8004432 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74704290 | ccaaggttgaagaca[C/T]acgcccaggacacgg | 9870 |
rs8005525 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | AREL1 | GRCh38.p7 | 14:74699687 | acttaattcttgttt[A/C]tatcaattagcctat | 9870 |
rs8005569 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74704927 | ATTTTTTAACAAGAA[C/T]TTTTTAAAACTCCTG | 9870 |
rs8007113 | snp | A/T | 0.41141 | 0.19091 | intron-variant | AREL1 | GRCh38.p7 | 14:74678953 | TGGAGTGTAGTGGCA[A/T]GATCACAGCTCACTG | 9870 |
rs8007335 | snp | A/C | 0.0744748 | 0.178019 | intron-variant | AREL1 | GRCh38.p7 | 14:74687396 | AACTGTGTGACCTAT[A/C]TAGGCTTCAGAATCT | 9870 |
rs8007734 | snp | A/G | 0.141258 | 0.225111 | intron-variant | AREL1 | GRCh38.p7 | 14:74687754 | agttctcaaagtttt[A/G]atgattattACAATT | 9870 |
rs8016694 | snp | C/T | 0 | 0 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662880 | GTCAGTGGCCCAAGC[C/T]GGCCATACTTCAGTG | 9870 |
rs8017229 | snp | C/T | 0.404035 | 0.196909 | intron-variant | AREL1 | GRCh38.p7 | 14:74676897 | TGCCTTCCGGGCTCA[C/T]GCCATTCTCCTGCCT | 9870 |
rs8018237 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | AREL1 | GRCh38.p7 | 14:74672252 | AGGCCAGTAAGTAAA[A/C]TGCTCTTCCCTCGAT | 9870 |
rs8019690 | snp | A/T | 0.416545 | 0.186448 | intron-variant | AREL1 | GRCh38.p7 | 14:74668439 | CTAAAAATGTAAAAC[A/T]TTTTTTCTGTTGGTA | 9870 |
rs9323600 | snp | G/T | 0.443464 | 0.15834 | intron-variant | AREL1 | GRCh38.p7 | 14:74676990 | ATTTTTAGTGGAGAC[G/T]GGGTTTCACTGTGTT | 9870 |
rs9671386 | snp | A/G | 0.39121 | 0.2063 | intron-variant | AREL1 | GRCh38.p7 | 14:74684344 | TCACTAGTTCCTGGA[A/G]GGAGTTGAAAAACAA | 9870 |
rs10133086 | snp | A/G | 0.374 | 0.217081 | intron-variant | AREL1 | GRCh38.p7 | 14:74691264 | GGTCAAGGCTGCAGT[A/G]AGCCATGATTGTGCT | 9870 |
rs10136897 | snp | G/T | 0.372391 | 0.217992 | intron-variant | AREL1 | GRCh38.p7 | 14:74706689 | CAATATGTTGGACCC[G/T]AAAGATTCCAGAATG | 9870 |
rs10137269 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AREL1 | GRCh38.p7 | 14:74677000 | gagacggggtttcac[C/T]gtgttagccaggata | 9870 |
rs10137800 | snp | C/T | 0.372189 | 0.218105 | intron-variant | AREL1 | GRCh38.p7 | 14:74703583 | tacATTTGTATCAca[C/T]gcaaaatgtagtcct | 9870 |
rs10138739 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | AREL1 | GRCh38.p7 | 14:74698614 | CCATGGGAGAAGGAC[A/G]ATGCAATGTTGCAAG | 9870 |
rs10145366 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | AREL1 | GRCh38.p7 | 14:74700505 | AAATTTTagccgggc[A/G]cagtggctcacacct | 9870 |
rs10151249 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | AREL1 | GRCh38.p7 | 14:74677693 | tttttagtagagaca[A/G]cgtttcaccatattg | 9870 |
rs10151838 | snp | A/G | 0.279991 | 0.248195 | intron-variant | AREL1 | GRCh38.p7 | 14:74665452 | TTTTTAAATGAAACA[A/G]AGGACAAAACACACA | 9870 |
rs10162454 | snp | C/T | 0.396909 | 0.202282 | intron-variant | AREL1 | GRCh38.p7 | 14:74677915 | ACTGCAAACCCTAAG[C/T]AAAATGAAAAAAACT | 9870 |
rs10220473 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | AREL1 | GRCh38.p7 | 14:74668300 | CTTAAAACCATCATC[A/C]AGGAATATTTGTGTA | 9870 |
rs10438165 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74715051 | AGTAAGTCTAGCACA[A/T]CTATGTAGATGAAAG | 9870 |
rs10873272 | snp | C/T | 0.388021 | 0.208447 | intron-variant | AREL1 | GRCh38.p7 | 14:74679797 | tgtgccattgcactc[C/T]agcttgggcgtcaga | 9870 |
rs11407786 | in-del | -/A | | | intron-variant | AREL1 | GRCh38.p7 | 14:74691324 | ACCCTGTCTCCATTT[-/A]AAAAAAAAAAAAAAA | 9870 |
rs11537957 | snp | C/T | | | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74662962 | CCTAGGCATGCCCCA[C/T]TCTGGAGGCTACAGC | 9870 |
rs11537958 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74661736 | AGACTGGTGCCTAAG[A/G]ACCACCACAGGGATG | 9870 |
rs11621536 | snp | A/T | 0.00472811 | 0.0483911 | intron-variant | AREL1 | GRCh38.p7 | 14:74669848 | CTGCTTAGAACCACT[A/T]ATCCCTTCAACCTTA | 9870 |
rs11624308 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74695190 | gttcaagcgattctc[G/T]tgcctcagcctccct | 9870 |
rs11627017 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74693896 | AAATACAGCAACATg[A/G]ccgggcacagtagtt | 9870 |
rs11629369 | snp | A/G | 0.450609 | 0.149185 | intron-variant | AREL1 | GRCh38.p7 | 14:74695318 | CTCCTGACCACAGGT[A/G]ATTCGCCCGCCTCAG | 9870 |
rs11629377 | snp | C/G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74665379 | cggcctcctgagtag[C/G/T]tgggattacaggcgA | 9870 |
rs11844127 | snp | C/G | 0.402406 | 0.198172 | intron-variant | AREL1 | GRCh38.p7 | 14:74673233 | ACTGGTAAAGAAAAA[C/G]AAAGAAATTAATCTA | 9870 |
rs12323361 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74705003 | TTTCAAATTCAATGC[C/T]GCACATTACCATGCA | 9870 |
rs12323528 | snp | G/T | 0.440884 | 0.161442 | intron-variant | AREL1 | GRCh38.p7 | 14:74685365 | TACTCCTTGAAGGCA[G/T]ATTTTTGTCTTATTC | 9870 |
rs12323883 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | AREL1 | GRCh38.p7 | 14:74680339 | tttaagaaatgcaaa[C/T]taaaagcacaatgag | 9870 |
rs12433518 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | AREL1, FCF1 | GRCh38.p7 | 14:74713391 | TCTGGGTTATTTGAG[C/G]CAAGAAGGGAAGGCA | 9870 |
rs12434646 | snp | C/T | 0.44546 | 0.155869 | intron-variant, upstream-variant-2KB | AREL1, FCF1 | GRCh38.p7 | 14:74711990 | TATGACAGAGGTACC[C/T]ATTCCGTTCCCAGCT | 9870 |
rs12434824 | snp | C/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699383 | tgtgtgtgtgagaga[C/G]agagagagagagcaa | 9870 |
rs12587457 | snp | C/T | 0.461259 | 0.133677 | intron-variant | AREL1 | GRCh38.p7 | 14:74697438 | TAACTAAGGAGGTTC[C/T]AAGAATATATCAGAC | 9870 |
rs12589339 | snp | C/T | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74705627 | CCTTACTGAGTCACT[C/T]TAACCTGTGATGAGA | 9870 |
rs12879930 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699388 | gtgtgagagagagag[A/C]gagagagcaagagca | 9870 |
rs12879939 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74699403 | agagagagcaagagc[A/G]agagagagagagaga | 9870 |
rs12883800 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696944 | actccatcctgggtg[A/C]caaagcaagacttcg | 9870 |
rs12883923 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696936 | gccactgcactccat[C/T]ctgggtgacaaagca | 9870 |
rs12883924 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696984 | ataaaataaaataat[A/G]aaataaaataaatta | 9870 |
rs12883928 | snp | A/C | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696945 | ctccatcctgggtga[A/C]aaagcaagacttcgt | 9870 |
rs12883931 | snp | A/G | | | intron-variant | AREL1 | GRCh38.p7 | 14:74696990 | taaaataataaaata[A/G]aataaattagctggg | 9870 |
rs12884249 | snp | C/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74697123 | ccactgtactctagc[C/T]tgggtaacagagaga | 9870 |
rs12889955 | snp | A/G | 0.44858 | 0.151875 | intron-variant | AREL1 | GRCh38.p7 | 14:74706296 | TATTCCATTAACTGC[A/G]CCTGAAGTGGCAGGC | 9870 |
rs12892795 | snp | A/G | 0 | 0 | intron-variant | AREL1 | GRCh38.p7 | 14:74664645 | tttgtattgttagta[A/G]agtcgggctttcacc | 9870 |
rs12892937 | snp | C/T | 0.463881 | 0.12944 | intron-variant | AREL1 | GRCh38.p7 | 14:74702224 | aaccccacatttccc[C/T]ccaacattgccctag | 9870 |
rs12893245 | snp | A/G | 0.372189 | 0.218105 | intron-variant | AREL1 | GRCh38.p7 | 14:74702233 | tttccccccaacatt[A/G]ccctagcagaggttc | 9870 |
rs12893742 | snp | G/T | | | intron-variant | AREL1 | GRCh38.p7 | 14:74664639 | tttttttttgtattg[G/T]tagtagagtcgggct | 9870 |
rs12894665 | snp | A/G | 0.3748 | 0.216622 | intron-variant | AREL1 | GRCh38.p7 | 14:74689839 | AACCTGAGGTGATCC[A/G]CCTGCCTCAGCCTCC | 9870 |
rs12896320 | snp | A/G | 0.41023 | 0.191902 | intron-variant | AREL1 | GRCh38.p7 | 14:74677597 | ctgcaacctctgcct[A/G]tcgggttcaagcgat | 9870 |
rs17101802 | snp | A/G | 0.0763149 | 0.179815 | utr-variant-3-prime | AREL1 | GRCh38.p7 | 14:74663161 | CCTTAGAGGCAGTCC[A/G]GTGCCATGGCCTATG | 9870 |
rs17101845 | snp | C/T | 0.00783052 | 0.0620802 | synonymous-codon, intron-variant, nc-transcript-variant | AREL1 | GRCh38.p7 | 14:74670070 | GCCCACGAGCCGTCC[C/T]GCAAACTCATACATT | 9870 |