SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1866444 | snp | C/T | 0.286303 | 0.24735 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506388 | AGCTAGACCTGTCTT[C/T]ACAATATCAGAAATA | 93082 |
rs2118836 | snp | A/G | 0.474453 | 0.110094 | downstream-variant-500B | NEURL3 | GRCh38.p7 | 2:96497235 | GGAGAGGGCTATGTG[A/G]AGGGAATCCGAACCT | 93082 |
rs2279049 | snp | C/T | 0.0441095 | 0.141807 | downstream-variant-500B | NEURL3 | GRCh38.p7 | 2:96497432 | TCCTTAAGTCCCAAC[C/T]AGACTTTTTGCCCTT | 93082 |
rs2579504 | snp | A/G | 0.00636936 | 0.0560724 | | | GRCh38.p7 | 2:96506548 | CAGGGCACTCACAAG[A/G]CTCCAAACCCACCAG | 93082 |
rs2579505 | snp | A/G | 0.392881 | 0.205147 | | | GRCh38.p7 | 2:96502225 | CCTGCTGGGATTCGC[A/G]GGAAGGGATGAGTGC | 93082 |
rs3731937 | snp | C/T | 0.177492 | 0.239254 | missense, utr-variant-5-prime, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96500559 | GTGGACCGCCGCGGC[C/T]GCCTCTTCGCCAAGG | 93082 |
rs3731938 | snp | C/T | 0.417954 | 0.185179 | synonymous-codon, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96500467 | CGTGATGGACGTGTA[C/T]GGGACCACTAAGGCC | 93082 |
rs3731939 | snp | A/G | 0.26326 | 0.249648 | intron-variant, missense | NEURL3 | GRCh38.p7 | 2:96499206 | CATCTCTGCCTTCGA[A/G]AGCATTTGCCTACTC | 93082 |
rs4440007 | snp | C/T | 0.0486741 | 0.148216 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506873 | TGCATCAGTGGGACC[C/T]TGGGCCATGAGGCAG | 93082 |
rs11440689 | in-del | -/G | 0.000399281 | 0.0141238 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504280 | TCCTCATCCCGCCTC[-/G]GGGGAAGCCCTCAGA | 93082 |
rs13025635 | snp | A/T | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96503893 | CACAGGGTTCAGATC[A/T]TCCTGGTGCCCAAGC | 93082 |
rs28603323 | snp | C/T | 0.228547 | 0.249078 | intron-variant | NEURL3 | GRCh38.p7 | 2:96501006 | CCCAGTATCCCAGAG[C/T]CCCTCACACCTGGGA | 93082 |
rs33928971 | in-del | -/T | 0.394904 | 0.203722 | intron-variant | NEURL3 | GRCh38.p7 | 2:96498751 | AGAGGTAATGGGTGC[-/T]TTTTTTTTAACTTTC | 93082 |
rs34146287 | in-del | -/C | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96499034 | CTCCTGCCTCGGCCT[-/C]CCCAAAGTATAGGGA | 93082 |
rs35060415 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506668 | TACGTCTCCACCTTA[-/G]TGCAGGCTGCCTTGG | 93082 |
rs35500772 | in-del | -/C | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96501038 | ACCTTGACCTTCCCC[-/C]TAGGGACCATTTCCA | 93082 |
rs35970487 | in-del | -/T | | | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96509644 | AAACGCTCCGCCAGG[-/T]ACTGCACCTGTGTCC | 93082 |
rs71427082 | snp | C/T | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503721 | GTGTGATCACCACCT[C/T]CACTCCACCTGCCTC | 93082 |
rs71427083 | snp | C/T | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503736 | CCACTCCACCTGCCT[C/T]CTCCCACGAGGCCTG | 93082 |
rs71427084 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96509036 | CCCCGGGTCTGCCGC[C/T]TAAGCAGCCCTGTCC | 93082 |
rs74856235 | snp | C/T | 0.216649 | 0.247765 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503649 | CAGGACCGTGTCCAC[C/T]GACTTCATACAGGGC | 93082 |
rs74936363 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96507156 | TGAAGACACAGGGAC[A/G]GAGAGAAGAATCTGA | 93082 |
rs76037051 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96505990 | GACAGTCACTGCAAA[C/G]GTCTAGCTCCCAATG | 93082 |
rs77860518 | snp | C/T | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504876 | GAGCGAGACTCCGTC[C/T]CAAAAAAAAAAAAAA | 93082 |
rs78179615 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96510053 | GTCAAGGGAAAGGTG[A/T]GCCCTCTCTTCTTTT | 93082 |
rs78697743 | snp | A/C | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504882 | GACTCCGTCTCAAAA[A/C]AAAAAAAAAAAAAAA | 93082 |
rs78987811 | snp | A/G/T | 0.0150278 | 0.0853725 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499482 | ACTCAGGTCCAGGAC[A/G/T]GCAAGCCCAGGTGCC | 93082 |
rs79559370 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506225 | CCCGACTTTTTTTTT[G/T]GAGACAGGGTCTCAC | 93082 |
rs80299835 | snp | C/G | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96504280 | CTCCTCATCCCGCCT[C/G]GGGGAAGCCCTCAGA | 93082 |
rs111510035 | snp | C/G | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504351 | AGAAAGTGGGGGATC[C/G]CAGCGCTGCTCCTGG | 93082 |
rs112487044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504435 | CCATTACTGTGACAG[C/T]AGCAGTGGCTCTTGG | 93082 |
rs112886119 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96507261 | TCATGAAACCAACGC[A/G]TAAAAATACATGTCC | 93082 |
rs113752553 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | NEURL3 | GRCh38.p7 | 2:96505507 | CTGCTGGAGCTGGCC[A/G]GCCTAAGAGAAGGAA | 93082 |
rs113842413 | snp | A/G | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504064 | GTGGACTGCCTGCGG[A/G]CTAAGCAGGGCCTCT | 93082 |
rs113967430 | snp | A/G | 0.5 | 0 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499899 | AGGAGGCGGGGAGTG[A/G]ACCACCACCCGGCCC | 93082 |
rs114059069 | snp | A/G | 0.0252325 | 0.109451 | nc-transcript-variant, utr-variant-5-prime | NEURL3 | GRCh38.p7 | 2:96507834 | AAAAAGGTCCTGTTT[A/G]TTGTAATCATTTCCA | 93082 |
rs114077132 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96505764 | ACTGCAGCAGACCCT[A/G]GCACACAGAAGGAAC | 93082 |
rs114238232 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499822 | TCCAGACCCAGCAAA[A/T]CAGGTGCTTCAGGTG | 93082 |
rs114330485 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96510006 | AGCTTCCAGGCCTGG[A/C]GTGGCTGCTCATGCC | 93082 |
rs114436195 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506014 | CCCAATGTGTTAGCA[C/G]TGGAAAAGAAGCCAA | 93082 |
rs114588931 | snp | C/T | 0.0197687 | 0.0974348 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96508394 | CCCCTCTGTTGCAGT[C/T]GGCCTCTCTTGCCCA | 93082 |
rs114659497 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96497737 | ATGTTTTAAATCATC[C/T]TCAGATGCATGGTCT | 93082 |
rs115561660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, missense | NEURL3 | GRCh38.p7 | 2:96499241 | GTTGCTTTTAGGTTT[C/T]CAGTAGGCAGAGCCA | 93082 |
rs115700792 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | NEURL3 | GRCh38.p7 | 2:96507595 | TCAGCCTCCCAAGTA[A/G]CTGGGACTGTGGCGC | 93082 |
rs115747136 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503222 | GGAATGGCCTTGAGG[A/G]TGCATGAGGCCCTGG | 93082 |
rs116087310 | snp | C/T | 0.013341 | 0.0805763 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499345 | CAGGTGCTGGATTCC[C/T]GGGGAGTCCCTGATT | 93082 |
rs116097873 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NEURL3 | GRCh38.p7 | 2:96501606 | AAGTCCCAGGTTAGC[C/T]CCTCAGAATCCTGGG | 93082 |
rs116116323 | snp | A/G | 0.00579415 | 0.0535117 | missense, utr-variant-5-prime, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96500526 | CCTCACGCAGCAGGA[A/G]CCGGCAGCCGGCGTT | 93082 |
rs116592375 | snp | A/G | 0.0539704 | 0.155153 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506363 | GGTGCATTCCACCAT[A/G]CTCAGCTAATATTTC | 93082 |
rs116766998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEURL3 | GRCh38.p7 | 2:96502053 | TTGCGGTGACAGTGA[C/T]TCTGTCCCTGACTTC | 93082 |
rs117082015 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506629 | AATCAGTGACTGCTC[A/G]GCTAAGGGATGGCTA | 93082 |
rs117373593 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96508619 | GCCCAGGGACGCCTA[C/G]CTATGACACTTGCCA | 93082 |
rs138288352 | snp | C/T | | | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506105 | GTGGCTTACTCTAAC[C/T]TAGTGCTCCTCACTC | 93082 |
rs138355687 | snp | C/T | 0.00558742 | 0.0525594 | synonymous-codon, missense, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96498283 | AGCAGGAGGGCCCTG[C/T]GCAGGGGCTACCGCC | 93082 |
rs138420615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499910 | AGTGGACCACCACCC[A/G]GCCCAGGAATGCCAA | 93082 |
rs138836829 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499001 | CAGGCTGGTCTCAAA[C/T]TCCTGGGCCCAAGCG | 93082 |
rs139538295 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NEURL3 | GRCh38.p7 | 2:96501925 | AGGCCACTCCCCTCC[A/C]AGATCAGGTCACACT | 93082 |
rs139545015 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96508481 | CTCCGGGAAGAGCCT[A/G]GCACACGAGGAAGCC | 93082 |
rs139688340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEURL3 | GRCh38.p7 | 2:96502898 | GATGAGGAGTTCTCC[C/T]AGCCTCACCCAGTGC | 93082 |
rs140423057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504967 | GTGGCCTCAGGTGAG[A/G]CTTGCAGAGAACCTT | 93082 |
rs140945375 | snp | C/T | 0.000514224 | 0.0160265 | missense, synonymous-codon, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96498305 | GCTACCGCCTCTATC[C/T]GCCAGCGGCACACAG | 93082 |
rs141291888 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NEURL3 | GRCh38.p7 | 2:96497220 | CATTTGGGGCACAAT[A/G]GGTTCGGATTCCCTT | 93082 |
rs141647788 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NEURL3 | GRCh38.p7 | 2:96501004 | CCCCCAGTATCCCAG[A/G]GTCCCTCACACCTGG | 93082 |
rs142682766 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NEURL3 | GRCh38.p7 | 2:96507514 | CTGTGGCCCAGACTG[C/G]AGTGCAGTGGCACGA | 93082 |
rs142905774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NEURL3 | GRCh38.p7 | 2:96500011 | GGGATGGCTCTCTTT[C/T]CCCCCCCACTGACTG | 93082 |
rs142972175 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506316 | GCTCAATTGATCCTC[C/T]CACCTCAGCCTCCTG | 93082 |
rs143263279 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503704 | TCGGGGTGGCCTGAC[A/G]GGTGTGATCACCACC | 93082 |
rs144315911 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NEURL3 | GRCh38.p7 | 2:96502018 | CAGGAGGCTCCATCT[G/T]GTCAGGCACCAGGAC | 93082 |
rs144818237 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96507182 | TCTGAACAGGCTGGC[C/T]GACTCTCCCCGGTTT | 93082 |
rs145100574 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506373 | ACCATGCTCAGCTAA[A/T]ATTTCTGATATTGTG | 93082 |
rs145130630 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503409 | GGTCATTCCGCAGCC[A/G]GGGCATCTAAGCAGC | 93082 |
rs145202138 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503310 | CCGATCCCTGCTTCA[C/G]GAGCCTTCTCAGCAG | 93082 |
rs145261873 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96508624 | GGGACGCCTACCTAT[A/G]ACACTTGCCAGCCCT | 93082 |
rs145692940 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506053 | TAGCCCGTCAATATT[C/T]ATTTCGGTTAGGAAA | 93082 |
rs145836227 | snp | C/T | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96499713 | GCCCTCCAGCCGCTG[C/T]CTGAGTGGAGACCCT | 93082 |
rs146159708 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NEURL3 | GRCh38.p7 | 2:96500018 | CTCTCTTTTCCCCCC[A/C/T]ACTGACTGAGAGGCT | 93082 |
rs147011146 | snp | A/G | 0.00438332 | 0.0466095 | downstream-variant-500B | NEURL3 | GRCh38.p7 | 2:96497498 | TCCATGGGCCCGAGC[A/G]CCCAGAGGCCCACCC | 93082 |
rs147383173 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96508373 | TGGGTGGTAGCCTCA[C/T]TGGGACCCCTCTGTT | 93082 |
rs147634459 | snp | C/T | 0.0119091 | 0.0762411 | downstream-variant-500B | NEURL3 | GRCh38.p7 | 2:96497568 | GCATGTCTCCAAATG[C/T]TGCATCATCCCGAAC | 93082 |
rs147785749 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NEURL3 | GRCh38.p7 | 2:96502420 | GCCATGGCTAACACC[C/G/T]CCATTCCAGGCCTGC | 93082 |
rs148612879 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEURL3 | GRCh38.p7 | 2:96507388 | TTATAGGTGTCCTAG[C/T]CATGAACCGAGCAAT | 93082 |
rs148787671 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96500763 | CCTCCCGCAGCACTC[G/T]CAGCGCCACACGCTC | 93082 |
rs149106733 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503637 | GGCAAGGGCCCACAG[A/G]ACCGTGTCCACCGAC | 93082 |
rs149375652 | snp | A/C/T | 0.000545642 | 0.0165085 | intron-variant | NEURL3 | GRCh38.p7 | 2:96499481 | AACTCAGGTCCAGGA[A/C/T]GGCAAGCCCAGGTGC | 93082 |
rs150189833 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96498348 | TATCGCTGAAGACCC[A/G]CCAGGCACAGTATCT | 93082 |
rs150503646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NEURL3 | GRCh38.p7 | 2:96501015 | CCAGAGTCCCTCACA[A/C]CTGGGAGCACCTTGA | 93082 |
rs180770931 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506322 | TTGATCCTCCCACCT[C/T]AGCCTCCTGAGTAGC | 93082 |
rs181134507 | snp | C/T | 0.000152847 | 0.00874071 | utr-variant-5-prime, intron-variant | NEURL3 | GRCh38.p7 | 2:96505313 | CCTCGGGCACAGGTC[C/T]CCAGGTCTAGAAGGA | 93082 |
rs181653330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NEURL3 | GRCh38.p7 | 2:96501170 | GAAAGAGTAGGGTTA[C/G]TCAGGCATAAATATC | 93082 |
rs181796849 | snp | C/G | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96500967 | TGCTAACCGGGTCTG[C/G]ACCCACCAGCTCCCC | 93082 |
rs182513643 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NEURL3 | GRCh38.p7 | 2:96497285 | GCAGCCACAGAGCAG[A/G]GGACAACAGCAAAGT | 93082 |
rs182561217 | snp | A/G | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96504971 | CCTCAGGTGAGGCTT[A/G]CAGAGAACCTTTGTG | 93082 |
rs182567739 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant, utr-variant-5-prime | NEURL3 | GRCh38.p7 | 2:96507917 | CACTAGGCATGACGT[A/G]ACAGGCTGGGATTGG | 93082 |
rs183130356 | snp | C/G | | | intron-variant | NEURL3 | GRCh38.p7 | 2:96502370 | TGTGCCCATGGTTGA[C/G]GCTGCTCCATGGAGG | 93082 |
rs183264030 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | NEURL3 | GRCh38.p7 | 2:96498109 | CTCCCTGCCTTCCTC[C/T]CTCTGCCGCACCTCT | 93082 |
rs183378905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEURL3 | GRCh38.p7 | 2:96503206 | GGAGGGGAACTCCCC[C/T]GGAATGGCCTTGAGG | 93082 |
rs183456454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NEURL3 | GRCh38.p7 | 2:96502027 | CCATCTGGTCAGGCA[C/T]CAGGACACGTTTGCG | 93082 |
rs183748994 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | NEURL3 | GRCh38.p7 | 2:96509015 | ACCCAGTCCAGGCCT[A/G]TGCTTCCCCGGGTCT | 93082 |
rs183892346 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NEURL3 | GRCh38.p7 | 2:96504942 | ATGGCTCTTCCACTA[C/T]GGGACACCTGTGGCC | 93082 |
rs184056618 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NEURL3 | GRCh38.p7 | 2:96506938 | AAAACCTGCCTAAAG[C/T]CTCCCGTCCAGGGTA | 93082 |