SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs148233816 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810345 | TTCCTGTATCCTAGG[C/T]GTTGGTTTGTTCCAT | 115677 |
rs148257202 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850661 | CTCATGCCTGTAATC[C/G]TAGCACTTTGGGAGG | 115677 |
rs148321070 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795755 | AGCTTATTTTGTGCA[A/G]TTTTTACAACCACAA | 115677 |
rs148347432 | in-del | -/TTTTAAAAGCCATC | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846715 | TACTCAAGGAATTAT[-/TTTTAAAAGCCATC]TGCAATATGTGTCAA | 115677 |
rs148372424 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864565 | GCTGGGATTACAGGC[A/G]TCACCCACCACGCCC | 115677 |
rs148395158 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805829 | CCGGTGCCATGGTCC[A/G]TAGCTCCTAGGAGAA | 115677 |
rs148455749 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825317 | AGATCATGAGTTGCA[C/T]AGCTGGATTCTTCCT | 115677 |
rs148510746 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821982 | TCTTTAAGTAGGTCA[C/T]GTAACTTCTTTTTAA | 115677 |
rs148551397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847860 | TTATTTCCTCCTCTT[A/C]TTATGAGCAAACATA | 115677 |
rs148602348 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841790 | ATTTGATCATAGTTT[C/T]ATGTGACATGGGAGC | 115677 |
rs148667190 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789816 | TCAGACCGAGAAACA[A/G]AGGGCCTTCAAGAAG | 115677 |
rs148684222 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800453 | TAATTCTCAGTCTGG[A/G]TTCAGCTGGGATGCC | 115677 |
rs148689961 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829518 | TAGAGACCAGGGATC[A/G]CTATGTTGGTCAGGC | 115677 |
rs148719196 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786275 | GGTGGTTGTTACACT[A/G]TTACAATCATTATTT | 115677 |
rs148719799 | snp | A/G | 0.00281452 | 0.0374077 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856699 | TTTCAGGCCTGGAAC[A/G]AATGCTTAAAACGTA | 115677 |
rs148763502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811756 | TTTCCAGAATGTGGT[A/G]TTATATTTTGGTACT | 115677 |
rs148773753 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851759 | TGTGCAACAAATTAC[C/T]GCTCCCCACCCCCAC | 115677 |
rs148810667 | in-del | -/TTATCT | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792443 | ATGTATAATATAAAA[-/TTATCT]TTATTTTATTTTATT | 115677 |
rs148830586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859097 | ATTCAATTTCATTTG[C/G]GTCTATTGATGTTAA | 115677 |
rs148849521 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797551 | TGGGCCAACATAAAG[C/G]TATAAGGACTTCCCA | 115677 |
rs148964342 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815327 | TAGCAGCTCCTAGAA[G/T]GCCTAATGCCAAAGT | 115677 |
rs149038541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823458 | AAATTTGTTCTGTGC[C/T]TCTGTCCTGGCTCCT | 115677 |
rs149059148 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835208 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGTGTGC | 115677 |
rs149172019 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850193 | GCTGGGATTATAGGC[A/G]TGAGCCACTGTGCCC | 115677 |
rs149218312 | snp | C/T | 0.00302602 | 0.0387795 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802597 | CCTTGATTACAGTGT[C/T]CAGAATGCTGGAGCG | 115677 |
rs149284256 | snp | A/G | 0.000152103 | 0.00871942 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851395 | TGAGTTCCTGTTAAC[A/G]GATTACTTTGTGAGT | 115677 |
rs149375166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799705 | ATTTCTCTTCCTAAC[A/G]CCAGTCTGCTGAGGT | 115677 |
rs149410502 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826709 | ATGTGCCTGACTTCA[C/T]TTTTTAAAAATCAGC | 115677 |
rs149443591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821727 | CAAAGGAGAATACCA[C/T]GTGGTTATGTAGCAG | 115677 |
rs149495811 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817301 | TTGCAGAGTCTTAGG[A/G]TCCTCTATGGAAAGG | 115677 |
rs149505968 | in-del | -/GCGCGC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834491 | AATCATTACTGGCGT[-/GCGCGC]GCGCGCGCGCGCACA | 115677 |
rs149567517 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825035 | AAGTTCTGGGATTAC[A/T]TGTGTGAGCCACCAC | 115677 |
rs149568681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795242 | CCCTGGAGACTAAAA[C/T]GACTCTATACTAGAC | 115677 |
rs149578176 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836207 | CGAAGAGGCGAACCC[A/G]GTCTGTTAAAATACT | 115677 |
rs149590043 | in-del | -/TATATATATGTGTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839914 | AAATATATATATATA[-/TATATATATGTGTG]TGTGTGTGTGTGTAT | 115677 |
rs149619829 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791066 | TTACCTATGTATACA[C/T]GTGCCATGTTGGTGT | 115677 |
rs149661704 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797235 | GCTGGGACTACAGGT[A/G]CGTACCACCATGCCT | 115677 |
rs149684643 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837519 | TTTCACCGAGTTAGC[C/T]AGGATAGTCTCGATC | 115677 |
rs149800806 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853928 | GCTGGAGTGTAGTGG[C/T]ACAATGTCAGCTCAC | 115677 |
rs149839787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808241 | CCCATTCCACGCTTG[A/T]TGTCCAGGGTCCCTT | 115677 |
rs149863316 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849203 | CGTGTTACCCACCAA[C/T]TTCTCCAAAGCCTTG | 115677 |
rs149926882 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829092 | CAAAGATGCTTTCTA[C/T]GCTTATTAGCTTGGT | 115677 |
rs150020594 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818414 | TCCTACCTCGGCCTC[C/T]GGAGTAGATGGGATT | 115677 |
rs150125341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790669 | GTTCCAGAGTGGAAA[A/C]TAAAGAAACATAGTG | 115677 |
rs150149198 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844950 | GGGAGAGCAAAGGCT[A/G]TATGGCAGGCGGAAA | 115677 |
rs150167180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858816 | GGGATAATGGTGAGG[A/T]GGGGGCTGGATAAGC | 115677 |
rs150177332 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787309 | TCCTCATCCCTCCCC[A/T]TGGGCACTGTCTCAG | 115677 |
rs150187568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799655 | GAGAGAACAGCCCTT[A/T]TCCGTCTAGAGTCTT | 115677 |
rs150210615 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839253 | ACCAACTCCTACTTT[C/G]ATTTTAGTTTTATTC | 115677 |
rs150309363 | in-del | -/T | 0.0482946 | 0.147699 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784663 | AAATTCTCCATTGGC[-/T]TTTTTTTTTTAATCT | 115677 |
rs150325271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855005 | TGGGCCATTAAAGGA[C/T]TCTAACTTGAACAAA | 115677 |
rs150351649 | in-del | -/CT | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820265 | TAGTGACTGACCCAA[-/CT]CTCTGTGCCTTGGTG | 115677 |
rs150367449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810525 | GTGAATGTGCCTGCT[G/T]CAATAGGAGGCACTC | 115677 |
rs150378259 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823217 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 115677 |
rs150401870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835837 | CTGTGTTTTCAGGCA[A/G]AATGAACACGAATAA | 115677 |
rs150427137 | in-del | -/T | 0.097727 | 0.198275 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835241 | ACCATGCTCGGCTAA[-/T]TTTTTTTTTGCATTT | 115677 |
rs150450833 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830909 | ATTGCACATGTTTAC[A/G]TGCTTTTTACATTCT | 115677 |
rs150498106 | snp | C/T | 0.226188 | 0.248863 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837378 | GCAGTGGCGCGATCT[C/T]GGCTTACTGCAAGCT | 115677 |
rs150534189 | in-del | -/CA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837119 | CATTCATGAGGGTTC[-/CA]CCCTCATGGCCTAAT | 115677 |
rs150536717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820416 | GTGTTGGATGTTCCT[A/G]TTTCTTGCCTAGGGA | 115677 |
rs150560054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833402 | TTTGATTCCCAAGCT[A/G]AAAAGCCAAGGAAGA | 115677 |
rs150588790 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832009 | TAAACACCACCTGGG[-/T]TTTGTTTTTTTCATT | 115677 |
rs150692267 | in-del | -/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840530 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 115677 |
rs150693172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789351 | ACATGGATGGGGAGA[A/C]CTCATAACCATGGCC | 115677 |
rs150696963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861411 | AGCACACACACACGT[A/G]TCACTGTACCTGCAT | 115677 |
rs150716432 | snp | A/T | 0.0115144 | 0.0749975 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168801194 | CCCTCCTCTCCACTC[A/T]TGTTGCAAGGCAAGT | 115677 |
rs150727232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816588 | CATTGCCTGGCTCCA[C/T]TCAACACATTCTTTA | 115677 |
rs150771614 | snp | A/C/G | 0.00478244 | 0.0486902 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796255 | CCAGGACTCAGAACC[A/C/G]GGAGTTGGCCTTCGG | 115677 |
rs150823417 | snp | A/C | 0.0379877 | 0.132479 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865521 | GCCAATATCATACTG[A/C]ATGGACAAAAACTGG | 115677 |
rs150885067 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812118 | ACCATTTTCAGCATC[A/G]TCTTCTTAGTACTAG | 115677 |
rs150906247 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824888 | CTCAGGTGATCCTCC[C/T]ACCCAGCCTCCCATA | 115677 |
rs150991063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786938 | TTCACCATGTTGTTC[A/G]GGCTGGTCTCGAATG | 115677 |
rs151013863 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825745 | AAGATTCTTGACTAA[C/T]GCATGCAGACGTGCC | 115677 |
rs151024220 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838880 | GCAACCTCTGCCTCC[C/G]AAGTTCAACAATTCT | 115677 |
rs151172773 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793602 | AGTGACAGAGTGAGA[A/C]CCTGTCTCAAAAAAG | 115677 |
rs151217103 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863576 | TCATTGCTTTAAAAA[A/C]TATTGTCTCCAAATT | 115677 |
rs151227881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789906 | GGTCTCATAAAAGAG[C/G]TTATGAGAGCAGAAC | 115677 |
rs151230649 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797677 | AGTGTTAACCTTAAA[A/T]TTTTTTTTTTTTTAA | 115677 |
rs151237874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803144 | GAGGAAGGATAGACT[C/T]CCCACTCTGCCTGGC | 115677 |
rs151255556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818247 | CAGCCTCAGACTCCT[A/G]TGCTCGCGAACTCCT | 115677 |
rs151279892 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857173 | TTTAGTTTTCTCATC[C/T]GCAAAATGGGGATAT | 115677 |
rs180852737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811418 | TATTTTAAGAACTCA[C/T]CCAAAAGGTATAAAT | 115677 |
rs180856889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850208 | ATGAGCCACTGTGCC[C/T]GGCCTCTAAAATGTT | 115677 |
rs180867585 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832841 | TGCCCAGGCTGATCC[C/T]GAACTCCTGGGCACA | 115677 |
rs180891878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791947 | TTGCCTGTTCACTCT[A/G]ATGGTAGTTTCTTTT | 115677 |
rs180935712 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824915 | CATATAGAGTAGCTG[A/G]GACCATGCCCTAAAT | 115677 |
rs180965597 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846373 | AATTCATTTTAGGGT[C/T]CTACGAAGTGTTCTC | 115677 |
rs180975673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788327 | CTTCTCTTCCTGAAC[G/T]GTTCAGTCCCTAAAC | 115677 |
rs180988112 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806219 | GTTCATTGTGTTAAA[A/T]TTAAGGGGAATATCA | 115677 |
rs180994832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837604 | GTGAGCCACCGCGCC[C/T]GGTCACAATATATCT | 115677 |
rs181023674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795762 | TTTGTGCAATTTTTA[C/T]AACCACAAAGTAATT | 115677 |
rs181035603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816083 | GTGCTGCCTTATAGC[C/T]GTGGAGTTTGTATGC | 115677 |
rs181083864 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820276 | CCAACTCTCTGTGCC[A/T]TGGTGTTCCGTTCCA | 115677 |
rs181085951 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849607 | GTAGTTCACCCGTCT[C/T]GGCCTCCCAAAATGC | 115677 |
rs181094322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832441 | ACTTGTTCTCTAAGT[A/G]TTGAAATCCTTTTTC | 115677 |
rs181101547 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802861 | GCTTTTTCTAGGAAA[C/G/T]GACAGGGCAGGTAAT | 115677 |
rs181123881 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863042 | AAGACAGACATACTT[A/C]CCAGATGCCACCTAG | 115677 |
rs181129495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842613 | AAGTGCAGGAGCCCA[A/G]AAGATTTACCAGATA | 115677 |
rs181142139 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790892 | GGAGCATTAGATTGG[C/T]AACTTATTCAGGACA | 115677 |
rs181154118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810587 | CTCAATATGGTGCCC[A/G]ACTGAATGCTGGCGA | 115677 |
rs181464255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856432 | ATACGAAAATTAGCC[C/G]GACATGGTGGCATAC | 115677 |
rs181506917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796765 | TCAGAGCCTCCCAAG[G/T]GCATTGGAGCCATTT | 115677 |
rs181542012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838374 | CCTCCCAAGTAGCTG[A/G]GAGTACAGGCGTGCG | 115677 |
rs181545342 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817957 | TCAAAAGACATACCA[A/G]TGAAGTTTGGATAGA | 115677 |
rs181594539 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861239 | TCTGTCTCCATAGCC[C/T]CCTCCAAACTCCCAT | 115677 |
rs181597971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841883 | AATACGGACATCCAT[A/G]TACAAATATTATGTA | 115677 |
rs181645559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820110 | GTTCCACTTCTCCCA[C/T]AATTCTCCATCTGCA | 115677 |
rs181653132 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801544 | TAGGGACTTTGAATG[C/G]AGCCTGCACACCAGG | 115677 |
rs181691417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805814 | CTAACTCAGATGGTG[C/T]CGGTGCCATGGTCCG | 115677 |
rs181713528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846142 | CCAGAAGGTCATTGA[A/C]TCACATATTACTCTA | 115677 |
rs181784828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834485 | ATTCCAAATCATTAC[G/T]GGCGTGCGCGCGCGC | 115677 |
rs181785224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168846816 | AGAAAATGATTCGAG[C/T]GGCTGCTTTCTCAGT | 115677 |
rs181800084 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825713 | CAAAGATAGTTCATT[C/T]GTGGTAATTTGCTAC | 115677 |
rs181851619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792376 | GTTTGGTGTAGTCAT[A/G]TGAGTTTTGTAAGTT | 115677 |
rs181853503 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865113 | ACAGCACTTTGCATT[C/T]ATGATTATTAGCTTG | 115677 |
rs181879592 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824287 | TGGTTTGCTTGATTT[A/C]CAGCCAGCATAATCA | 115677 |
rs181928173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817045 | TATTCAGTACAACCC[A/G]TAGACCAGCCACTGT | 115677 |
rs181957371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855882 | AATTAAATTCTGTAC[A/G]TAGAAGTTAGGCATG | 115677 |
rs182046475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812134 | TCTTCTTAGTACTAG[A/G]TATGATCATGTGTAA | 115677 |
rs182073385 | snp | C/G/T | 0.000231867 | 0.0107649 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851123 | AGAATTCAACTTTTA[C/G/T]GCAATAACTTAAACC | 115677 |
rs182153677 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853301 | TTTTATCCAGTGTTA[C/T]GAAATTTACATGGAC | 115677 |
rs182199461 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837962 | TATATTGCAGTTTCT[C/G]AAGATTTCTCTTCTG | 115677 |
rs182200466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820943 | AGGAAGAGGCTGTGA[C/T]TGACAGTGTTACCTT | 115677 |
rs182218899 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796237 | CCAAGGACTAGGCGT[C/T]GTCCAGGACTCAGAA | 115677 |
rs182222901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847906 | TTCCCTGAAATGTAA[C/T]TAAAATCTGTTAAGC | 115677 |
rs182245416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789888 | CCAGTACTTGGAAAA[A/G]CTGGTCTCATAAAAG | 115677 |
rs182260548 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784542 | GATTTGACCCCAGAC[C/T]GGAGTGATTCCAAAA | 115677 |
rs182266094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827960 | ATAACTGGGAAAAAA[A/G]CAGTATATATAATGA | 115677 |
rs182268801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858173 | ATTACCAGCATACAT[A/G]TATTAGGATCATCTG | 115677 |
rs182273198 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808235 | CATGCCCCCATTCCA[C/T]GCTTGATGTCCAGGG | 115677 |
rs182280921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803394 | AGTGTTTTATCCCAA[C/T]ACATGGGGCTGAAAA | 115677 |
rs182369397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793333 | AAATATTGGCCAGGC[A/G]CCATGGCTCACACCT | 115677 |
rs182385898 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835011 | TCAGGAAAAATGTAT[A/T]CTTGGAGCAAGGTTC | 115677 |
rs182392605 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813185 | GTATGACTCCTATGA[A/C]TTCAACTCATTACCC | 115677 |
rs182475854 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813985 | TCGTCTTGAGCTTTC[A/C]AGTTTCCTCCCCTTG | 115677 |
rs182488285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843339 | GCCAGAGTTTCTGCT[C/T]CTAATTCTTAGTGGA | 115677 |
rs182656084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797157 | GTGGTGGCATGAACA[C/T]GGCTTATTGCAGCCT | 115677 |
rs182664069 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839569 | AAGGAAAAGAAGTCA[A/G]TCTTTGACAAATTTT | 115677 |
rs182686272 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851539 | CCCATATAAATTTAA[A/G]AAACCCAGCATTCTA | 115677 |
rs182731595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863368 | AGTTAATAATTTCCT[G/T]TGTCTTAGAAAGAAA | 115677 |
rs182767741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793608 | AGAGTGAGACCCTGT[C/T]TCAAAAAAGAAAACA | 115677 |
rs182781345 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835458 | TTTCATGTGGGTAGT[A/G]ACAAACTCACAACCA | 115677 |
rs182793369 | snp | A/C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785246 | GGCCAAAGTTCCTGA[A/C/T]CCAGAGTGCTAGTTA | 115677 |
rs182902456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818600 | TACATTTTAATTAGC[A/G]CTTTATCTAAAATAT | 115677 |
rs182974045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860151 | TCGAAAACAATCTCA[A/G]TCATTTACAGGGTTG | 115677 |
rs182979417 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840432 | CTACTCAGGAGGCTG[A/G]GGCAGGAGAATGGCG | 115677 |
rs182986005 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819356 | TTAGACCGGAAGCAT[G/T]GAAGAGCCGTGGAAG | 115677 |
rs183055026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863774 | TTATAGCAGCCAACA[C/T]GCCAAACAATCAAAA | 115677 |
rs183077871 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803776 | TTATATATAGATTTT[G/T]AAGAGTGAAACTTCC | 115677 |
rs183105262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843510 | TTAGGCACTGGAGAT[A/C]CAGAGCATTGAATAA | 115677 |
rs183112497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821943 | GACTTGGGCTCTCAA[C/T]ACATTTTAATTTTCA | 115677 |
rs183172555 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822491 | GGTATTAGACTAGTT[A/G]TTAGAGAGCTCTGCC | 115677 |
rs183222240 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797296 | GAGATGGGGTTTTAC[C/G]ATGTTGCCCAGGCTG | 115677 |
rs183224483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863923 | TCTTTTTTTATTTTT[A/T]TTTTTGAGGCAGAGT | 115677 |
rs183256101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806739 | TATGGAGATGTAGAA[G/T]CAATAGTAGATTATT | 115677 |
rs183330488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847414 | CCTGGGAGCCTCTGA[A/G]TCAATCAGAGCCTCT | 115677 |
rs183344696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807232 | CCCACAAAGCAGGTA[A/G]GTTCCAAGATTTTCT | 115677 |
rs183424107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844531 | TGTTTTGTATTAATC[A/G]TGACATTATGAGAAC | 115677 |
rs183436136 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804441 | ATTTATTTGCAATTG[C/T]TTCATCTTAATCAAG | 115677 |
rs183513634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844733 | AAATTAGCCGCGCGT[A/G]GTGGCGGGCGCCTGT | 115677 |
rs183577433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826959 | TTTCTGGAATCTCCT[A/G]TAATTGTAAGTATAT | 115677 |
rs183579560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804527 | GTGAAGATGAATCTG[C/T]GGTTTGGGAACAAAA | 115677 |
rs183583988 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785907 | AGGTGCATGCCACCA[A/C]ACCCAGCTAATTTTT | 115677 |
rs183640232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789150 | TCTTTTTGGGCCAGA[A/G]AGCAAAGTAGTACTT | 115677 |
rs183678804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788672 | GGATTGATCAAAGGC[A/G]TAAATATATTAACAA | 115677 |
rs183760365 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785096 | AGGGGTGGGTAGTAG[A/G]TGAGGGATGAAATGC | 115677 |
rs183826942 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849748 | GCCCAAAGTCCCCTG[A/G]GCACATACCCAGCAG | 115677 |
rs183833256 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791352 | GCTGCATAGTATTCC[A/G]TGGTGTATATGTGCC | 115677 |
rs183833544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832531 | ATAACTAGAGACAGA[C/T]GCACTCAGAGACAGG | 115677 |
rs183840388 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810918 | TAAATCAAATGACAA[A/C]AACTTTTACTGGAAA | 115677 |
rs184063284 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858510 | GTCATAAGAAAAATT[A/G]TTGAGAAAACTGGAG | 115677 |
rs184074292 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818783 | TTAGAATGTAAAGGG[A/T]TTAAAAGTCAGTGCA | 115677 |
rs184171070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816184 | TTTACTCTGACAGAG[C/T]TGTGCCCCTTTAGAA | 115677 |
rs184207443 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855574 | GGTCTTCTCATTTAA[A/G]GAACCATATATCAAA | 115677 |
rs184217342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840258 | TATGTCAGCTGGGCG[C/T]GGTGGCTCACGCCTG | 115677 |
rs184304356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837605 | TGAGCCACCGCGCCC[A/G]GTCACAATATATCTT | 115677 |
rs184311803 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864687 | TATACACAGGTGTTC[A/G]ATACATTTGGCTTCA | 115677 |
rs184328104 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854393 | AGTCATTAGTTTCCC[A/G]TCTTTCTCCATGGGT | 115677 |
rs184335060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824021 | TGGAGGTTACAGTGA[A/G]CCAAGATTGTGCCAT | 115677 |
rs184338873 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837340 | TTTGAGATGGAGTCT[A/T]GCTGTGTCGCCCAGG | 115677 |
rs184341888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794921 | TTTTAACAGGTATTG[A/C]AGGCACAGCATATAA | 115677 |
rs184345340 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815236 | TGCAATTCATGGTCA[A/T]GCTTAGCTTCTTTTA | 115677 |
rs184351653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840651 | GTGAATGGTATTAAC[A/G]TTCAACATTTTGGAT | 115677 |
rs184365209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864743 | CTACCAAGTAAATCC[C/T]TGAAGCAGAACCTCC | 115677 |
rs184374201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798962 | CTTGCTCTGCCTCCT[G/T]GAACCCACACCTAGA | 115677 |
rs184377613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845370 | CATCTTCCAGGCACC[C/T]ACCCTTCAAGGGCTA | 115677 |
rs184393781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795946 | CTGTGGGCAAAGGCC[G/T]AAACCCTTAAAAAAT | 115677 |
rs184483220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798081 | CTAATGCTATGTAAA[C/T]GTTATATAAATAGTC | 115677 |
rs184492359 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819677 | GTTCCCAAAATGGTC[A/T]TTAGGATTTAAAATG | 115677 |
rs184520729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860516 | TCTCTACTAAGAATA[C/T]AAAAATTAGCCAGGC | 115677 |
rs184599166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794141 | CTCCTTGGATCTCTC[A/G]TTAATGCCTGGAACA | 115677 |
rs184661066 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856586 | TCTTAAAAAAAAAAA[A/T]CTCACTGGTATCACT | 115677 |
rs184836372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830110 | CCTTCTGCCTTTGCA[A/G]GCCAACTTAATAAAA | 115677 |
rs184866040 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819884 | CCCATCCTTCCCACT[C/T]TGCCAGACCCTCAAC | 115677 |
rs184868836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848089 | AAAACAGAAGAGCTG[A/C]TTTCTAGATCTTTTT | 115677 |
rs184875234 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800894 | CTCAGTCTATATCCT[G/T]TCTCTAAATTTCTTT | 115677 |
rs184878852 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865153 | GAAAAAAGATGGATG[G/T]GTGGAGACAGACAAG | 115677 |
rs185001180 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846191 | TATGTTTATGGCACT[C/G]AAGTGTCAAATGTTA | 115677 |
rs185034028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848865 | AGAGATGAATTATGG[C/T]GGTGTTTGCATAATA | 115677 |
rs185099973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810333 | ATGGTAAGACTGTTC[C/G]TGTATCCTAGGCGTT | 115677 |
rs185150972 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832018 | CCTGGGTTTTGTTTT[A/T]TTCATTTGTAGAAAG | 115677 |
rs185166033 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806414 | TAATCTTTACAAGTC[A/C/G]CCTGTCTAAACATTT | 115677 |
rs185181994 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805687 | CCCTCCCCGCATGTC[A/G]TCGGCCATTGAAATG | 115677 |
rs185186170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836716 | AAGTCAGCACAGCCA[A/C]CTGCCTACTGAAGTA | 115677 |
rs185196372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790768 | GAACTCAGGGTTAGA[C/T]AGTAGTGATGAATCC | 115677 |
rs185203685 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846486 | ATACTGTGAGAAATA[C/T]TGTAAAGCCTCAAAT | 115677 |
rs185205435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788370 | AGAGCAGAGCAGATA[C/T]CTCTGCTAGGTGAGG | 115677 |
rs185207284 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824916 | ATATAGAGTAGCTGG[C/G]ACCATGCCCTAAATT | 115677 |
rs185296070 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853719 | TGGGGGTGTGATGTC[A/C]GCTTGCGCCTCAGCT | 115677 |
rs185314523 | snp | A/T | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786629 | AAAAGGGATGCAAGA[A/T]CCCAGAGGTATGCCA | 115677 |
rs185361778 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814302 | TGTTAAACCATATCA[A/T]CAAGGATGGATGGTC | 115677 |
rs185577967 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818405 | TAATGATTCTCCTAC[C/T]TCGGCCTCTGGAGTA | 115677 |
rs185604652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796768 | GAGCCTCCCAAGTGC[A/G]TTGGAGCCATTTCCC | 115677 |
rs185611802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856471 | TCCCAGCTACTCAAG[A/G]GGCTGAGGGAGGAGA | 115677 |
rs185617235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838868 | TCTGGGCCGACTGCA[A/G]CCTCTGCCTCCCAAG | 115677 |
rs185667857 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860652 | CTCCAGCCTGGGTGA[C/T]AGGGCAAGACTCTGT | 115677 |
rs185718731 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792526 | GCGATCTTGACTCAC[C/T]GCAACCTCTGTCTCC | 115677 |
rs185723968 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820258 | CTCAGGCTAGTGACT[A/G]ACCCAACTCTCTGTG | 115677 |
rs185732059 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801802 | CAATAGAACTCAAGC[C/T]GTGGTTGAGTTCTTG | 115677 |
rs185736695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790592 | AGGACGTTACATAAA[A/G]TAATTAACTGGTCAT | 115677 |
rs185759635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861599 | AGCTAGGGATGATGA[C/T]AACATGCACATGCCC | 115677 |
rs185760501 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858425 | GAAACTTTTATTTAC[A/T]TTCTTCCTTATTTCA | 115677 |
rs185763332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842513 | AAGTAAAATAATATC[A/G]CTAGATAGGACAGTA | 115677 |
rs185844863 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809591 | AACAAAGAGGTTAAA[A/C]AAGTTTCTTTACTGC | 115677 |
rs185863057 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841617 | AATAATTACACTCGC[C/T]AAATTTTGAGTGCTA | 115677 |
rs185870746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796295 | TAAGGTGTGTCAAGA[C/T]GTGTCACCCATGTCA | 115677 |
rs185903901 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817344 | CATGAAGCCCAGTGG[A/C]TTTCAAACCTTATAG | 115677 |
rs185907330 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839680 | GCACTTCGGGAGGCT[G/T]AGGTGGGCAGATTAC | 115677 |
rs185989448 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802904 | TTCTCATATTCTTGG[A/G]AAAAGTTTTGAGAGA | 115677 |
rs186110121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820778 | CCTTTTTCATACCAC[A/C]AAAGCCCAACTTTTT | 115677 |
rs186320622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842643 | AAGACTATGGGATTC[A/G]TTGGCCAATTGCAAT | 115677 |
rs186400102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168846850 | CCCAAGGATGGCACT[G/T]GAGTAGTCCCACTCT | 115677 |
rs186462378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829182 | ATTAAACAATCCTTT[C/G]AGGGGCACCTGGTCC | 115677 |
rs186469874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808492 | GCAGAAGAATTTACT[C/T]CGTAAACATGCATCC | 115677 |
rs186482531 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790292 | TATGATAAAATTAAT[A/G]TATAATAAACTGAAA | 115677 |
rs186487139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863107 | ACAATAAATTGATTA[A/T]CTTGTTTTCAGTTCT | 115677 |
rs186487435 | snp | C/T | 0.000714232 | 0.018884 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824725 | AGAAAAAGGTAAGTA[C/T]TGTGGCAGAGGTAAG | 115677 |
rs186510622 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788079 | AAAAAAATGATGTAA[A/G]TAGTAACGATGACAG | 115677 |
rs186515932 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848021 | TGCCCACTAGGGATG[C/T]AATATGTTCTAAAAC | 115677 |
rs186519449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803481 | ACACAAACTGTGGGG[C/T]GGCAGATAAATGGGC | 115677 |
rs186521101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850471 | GGCCTGTCATTCTCT[C/T]CCCTGCAGACTAGCA | 115677 |
rs186538810 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843401 | CTGTCAAAGTGAAGC[A/G]TAAATTAAGGCTTAA | 115677 |
rs186539726 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784671 | CCATTGGCTTTTTTT[G/T]TTAATCTACCTCCGT | 115677 |
rs186550719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821085 | TATTAGAAGAATTAA[C/T]ATTTATTAAGGATGA | 115677 |
rs186551341 | snp | A/G | 0.000895968 | 0.0211467 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851246 | CAGAAACCTTTCTTC[A/G]ACAACCTTATTCTGT | 115677 |
rs186639299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812799 | GAAAGGCAGAGAGAG[G/T]GGCAGAGTGTGTCCC | 115677 |
rs186746398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806075 | GGATTCCAAATACTA[C/T]GCAGATGGTGAACAA | 115677 |
rs186787978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838043 | CTCTTGATATCAGGT[A/G]CTCGATAAATAATAC | 115677 |
rs186850103 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834811 | CAGCTAATACCCCAA[A/T]TAAGTAAAAATAAAT | 115677 |
rs186965123 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835235 | GTGCACCACCATGCT[C/T]GGCTAATTTTTTTTT | 115677 |
rs186971650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813361 | ATAGAAGACAGGCAA[C/T]AGATGATGCCTGCTG | 115677 |
rs186989123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788679 | TCAAAGGCGTAAATA[C/T]ATTAACAATAAGGGG | 115677 |
rs187003984 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793335 | ATATTGGCCAGGCGC[C/T]ATGGCTCACACCTGT | 115677 |
rs187009426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851880 | CTCCCAAGGCTGCAA[C/T]CAAGGTATCAGGTTG | 115677 |
rs187157922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789366 | CCTCATAACCATGGC[C/T]GAAGGCAAAAGGCAT | 115677 |
rs187159956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806763 | GATTATTCCCTGGAA[C/T]GAATATTTGATAGGG | 115677 |
rs187226539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860271 | GAATTGGAAACACAG[A/G]CTATAAAGTATAGTA | 115677 |
rs187228015 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840462 | GTGAACCCCGGAGGC[A/G]GAGCTTGCAGTGAGC | 115677 |
rs187236890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819548 | CCGTTCAGCGCTAGA[A/G]GCCTGGGAGAGGTTT | 115677 |
rs187322039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832948 | TTGTTTTTAAAAATC[A/C]ATTTTCTTTTAATAT | 115677 |
rs187348928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814654 | GGTTATGACAGACAA[C/T]GATGAAGGCAAATCT | 115677 |
rs187350099 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863472 | GATCCTGACGGGGGC[A/C]GATGATCCTGAAGGG | 115677 |
rs187355016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843848 | TTTTTAGGCATATAT[C/T]CTACAGAAAAATGTA | 115677 |
rs187356834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826474 | TCCCTTGCTTCCTTC[A/G]TTCCTTCTCTTTCCA | 115677 |
rs187363326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856194 | CACTTCTCAAATTTC[A/C]TTAAGTGAAGAGAAA | 115677 |
rs187367586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822043 | AGAGATCTCCTGGGG[C/T]TCCAGAGCATCTGAG | 115677 |
rs187386875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794642 | AGGCGTGAGCTACCA[C/T]GCCCAGCCCAGCGGA | 115677 |
rs187388180 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863858 | AATCCATCAGCTACA[C/G/T]AGAAATAGAAAGTGA | 115677 |
rs187500888 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818752 | ATATTGACCAGCCTT[C/G]CATGCTGAGAGAAAA | 115677 |
rs187593195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811447 | ATGCCTGTAGCTGCA[C/T]GATCCTTTATAATGA | 115677 |
rs187739244 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797232 | ATAGCTGGGACTACA[A/G]GTACGTACCACCATG | 115677 |
rs187845028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864699 | TTCGATACATTTGGC[C/T]TCATCTGAATCAAGT | 115677 |
rs187883160 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840337 | AGATCGAGACCATCC[A/G]GGCTAACATGGTGAA | 115677 |
rs187888431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797360 | CTACAGCCTCCCAAA[A/G]TATTGAGATAACAGG | 115677 |
rs187892448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818796 | GGATTAAAAGTCAGT[A/G]CATGTCACTTCCTTG | 115677 |
rs187956659 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844641 | TTTGGGAGGCAGAGG[C/T]GGGCGGATCAAGAGG | 115677 |
rs187974486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804466 | ATCAAGTGTTCAAGT[C/T]GATTTCCTGGCACAT | 115677 |
rs188102820 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798568 | CAGAGAGGCCATACC[A/G]GGAAGGCACATGCTG | 115677 |
rs188107531 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791889 | TGGATATTAGCCCTT[C/T]GTCAGATGAGTAGGT | 115677 |
rs188110460 | snp | C/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827280 | ACTCCCTAATCCTCC[C/T]GCTATGCCATGAGGG | 115677 |
rs188178671 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864116 | GGGACTACAGGCGTG[C/T]GCCACCATGCCTGGC | 115677 |
rs188211197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853921 | GGCCCAGGCTGGAGT[A/G]TAGTGGCACAATGTC | 115677 |
rs188241754 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785167 | ATAAAAGAGCAGTTC[C/G]CAGCCCTCCTCTTTT | 115677 |
rs188251837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822867 | GTTGGCTACCACTGC[C/T]GATTCCCATTAGAAA | 115677 |
rs188260037 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785500 | TTATAAAATAGTTTG[C/T]ACTATGCTAACCAGT | 115677 |
rs188332980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847562 | ACTTCTTCCTGTAGT[A/T]CCAGCCCAAAGGCTA | 115677 |
rs188404863 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807742 | GAGGTACGAGGCAAA[A/G]CCATGGGCCAGTTCC | 115677 |
rs188431645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849984 | GCAGTAGCATGATCT[C/T]GGCTCACTGCAAACT | 115677 |
rs188445132 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832532 | TAACTAGAGACAGAC[A/G]CACTCAGAGACAGGC | 115677 |
rs188453356 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811182 | CCAGAAATATTATTT[G/T]GAAGTTTATATGTGC | 115677 |
rs188487086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803792 | AAGAGTGAAACTTCC[C/G]CCTTTAATTACTTCA | 115677 |
rs188505325 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836734 | GCCTACTGAAGTAAT[A/T]GCATTTACATATCTG | 115677 |
rs188555437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862702 | AAGGTATTACGTAGT[A/G]GCTTTATAATGTAAA | 115677 |
rs188567112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842570 | TAAAAATTGTATGAT[C/T]CCACAAGTCTCTACC | 115677 |
rs188584661 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854468 | CTCTACCATCCTATT[C/T]TTTTTTATTCAATCC | 115677 |
rs188588452 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837371 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTTACT | 115677 |
rs188599224 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815304 | AAACAGATTTAGCCA[C/G]AGAAACATAGCAGCT | 115677 |
rs188615381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788131 | TGTAATTCAAGCACA[C/T]TGGGAGGCCAAGGCA | 115677 |
rs188648749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795002 | TCCCACACCCATCCA[C/T]CAGCCTCTCAGTTGC | 115677 |
rs188693674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848152 | TGTCACATAGGAGAT[C/G]CAAACAACTGAGCAG | 115677 |
rs188729187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810527 | GAATGTGCCTGCTGC[A/C]ATAGGAGGCACTCAG | 115677 |
rs188757000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810194 | CTTTAGAAATTAGCA[A/G]TTTCCTCATTAAAGC | 115677 |
rs188764127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790888 | TGAAGGAGCATTAGA[C/T]TGGCAACTTATTCAG | 115677 |
rs188844322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836198 | GGCAGCTTCCGAAGA[A/G]GCGAACCCAGTCTGT | 115677 |
rs188888041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793773 | ATCTTCCAAGCCTCA[C/T]GAACTATAAGGTCCC | 115677 |
rs188977496 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830397 | TTTATTTTCTAAAGT[G/T]ACCTTGTTCCACATT | 115677 |
rs189012850 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819786 | TGCAGGCAGAGAAAG[G/T]GTACAATCGTGCTGT | 115677 |
rs189033498 | snp | C/T | 0.000530003 | 0.0162702 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859540 | TAGACCTTTTGGAAG[C/T]GAACTCCTACAAACT | 115677 |
rs189085537 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838250 | TGTGTCTTTGAATAT[A/C]ATCACCCACCTATCC | 115677 |
rs189095191 | snp | A/G | 0.000729116 | 0.0190795 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864836 | TGTATTTTCACAGGT[A/G]ACATTGTGATTATAC | 115677 |
rs189097367 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845580 | ATCTCAGTTTCCTTT[C/T]CTCCTGTTAAGATCC | 115677 |
rs189120220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853341 | CAAAGAGACCAATCT[A/G]AGTGCAAAACTTGGA | 115677 |
rs189121958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856431 | AATACGAAAATTAGC[C/T]GGACATGGTGGCATA | 115677 |
rs189186804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813989 | CTTGAGCTTTCAAGT[C/T]TCCTCCCCTTGCTCA | 115677 |
rs189236725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819894 | CCACTTTGCCAGACC[C/T]TCAACATCCCCACTC | 115677 |
rs189244800 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801233 | TTAATTGTCCCCTGA[C/T]TCTTCTACGTTGTTT | 115677 |
rs189260997 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799257 | TAAATGCTCTACTTA[A/T]ATTAAGTTGGCCTCA | 115677 |
rs189263940 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861221 | CGTGAGGAGCTTTGT[C/T]GCTCTGTCTCCATAG | 115677 |
rs189273280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841798 | ATAGTTTTATGTGAC[A/G]TGGGAGCCTTCAGAA | 115677 |
rs189287947 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840704 | GTTAGTCAAAATGCC[A/C]TTAAATAGAGAGAGT | 115677 |
rs189347657 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860539 | AGCCAGGCATGGTGG[C/T]GGGCACCTGTAATCC | 115677 |
rs189386607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805142 | AAAGGGCTCATGGTA[C/T]GAAAAAATTTAAAAA | 115677 |
rs189401104 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786152 | GTAATTGCCAGAAAA[C/G]TTCAGAGGAGAGAGA | 115677 |
rs189417419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844920 | CTGCATTATGCTCCT[A/G]CCCCATTGAAAACTG | 115677 |
rs189475579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806138 | TTTGAAACATCACCC[C/T]CAGTGAATCAGAACT | 115677 |
rs189510801 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846343 | CACCATTCTTCTGTA[A/C]AAATTGAATATAAAA | 115677 |
rs189669203 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802189 | AGGAATTAGCTAACC[C/T]TCAGAGAGGCAGTCT | 115677 |
rs189677398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832392 | GGACTAGCAGTAAAT[C/G]TACTAACAAGATTCA | 115677 |
rs189773052 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865196 | TGGTTCCTAGAGGAG[G/T]TTCCAAATTCTAGGA | 115677 |
rs189791566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824908 | AGCCTCCCATATAGA[A/G]TAGCTGGGACCATGC | 115677 |
rs189798571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787550 | GAACACTTATCACAC[A/G]GCCTTCCCCACTGGA | 115677 |
rs189818860 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824085 | CATCTCAAAACAAAA[A/G]ACAAAAAAACAAAAA | 115677 |
rs189825778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852223 | GCATGGGTTCTAGGA[A/G]GTGGGAGTCACTATC | 115677 |
rs189835891 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835396 | CCTTCTCGATAATGT[A/G]ATTTGTTCATCAAAT | 115677 |
rs189896344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813484 | TCCCCACCTTGCCAC[C/T]GACATCTACTTTCTT | 115677 |
rs189924489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820260 | CAGGCTAGTGACTGA[A/C]CCAACTCTCTGTGCC | 115677 |
rs189926585 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849054 | AATACCATACTGAAT[A/C]AGGCCAATGGGCTCC | 115677 |
rs189966666 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827713 | GCTAGGACTATGGGC[A/G]TGCATCACCACACCT | 115677 |
rs189975226 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858149 | CTTGCACAGAATTTT[G/T]TCATTGTCATTACCA | 115677 |
rs189983518 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839048 | ACTTGGCCTCCCAAA[G/T]TGCTGGGATTACGGG | 115677 |
rs190037068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818407 | ATGATTCTCCTACCT[C/T]GGCCTCTGGAGTAGA | 115677 |
rs190077853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805794 | ATATCAGACAATGAC[C/T]GTCACTAACTCAGAT | 115677 |
rs190111513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834858 | TTGTTACATATAGTA[C/G]TTTATGTATTATGTT | 115677 |
rs190119650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812943 | ATGGGGCCAAAGAAA[A/G]ATATGAGCGAGCTGA | 115677 |
rs190132524 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792958 | TCCCAAAGTTAGCAT[A/C]CTAATTTGTAGTGTG | 115677 |
rs190438596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796099 | ATCAGAATGAGATTG[C/T]TTCTACACTTCCATC | 115677 |
rs190470395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837662 | TTTCCACTTCCTCAT[C/T]TTCTGTTCACTCTTC | 115677 |
rs190594611 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790644 | GAAAGCCAAGGAGGA[A/G]CTAAGAACTGTTCCA | 115677 |
rs190654971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855800 | GTCAACCAACTGTGC[A/G]TGAGAGTTTTGGATG | 115677 |
rs190657214 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817813 | CAGAATTAAGACAAT[A/C]GATAATGCTGCAGTG | 115677 |
rs190678151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796566 | TTCTAGACTCCAGCT[C/G]TCCCAAACTTATTCT | 115677 |
rs190724947 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816327 | CAAAGACTCCTATGA[A/C]CTTTAGGATAAAATT | 115677 |
rs190887604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863485 | GCAGATGATCCTGAA[A/G]GGGGCAGATCTTTCT | 115677 |
rs190895863 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843426 | GCTTAAGTGTTAGGT[C/G]CTTCAAAATTAGTTT | 115677 |
rs190904114 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821451 | TCATTCATTCATTTG[G/T]GACATACATACTGAG | 115677 |
rs190939428 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793566 | CAGTGAGCCAAGATC[A/G]TGTCACTGCACTCCA | 115677 |
rs190947833 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784978 | AATTCAGTCATTCAA[A/T]ACATTGCAGACTGAA | 115677 |
rs190953725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863271 | TGTCAATTTACTGAC[A/G]AGGGAGAACTTAGAG | 115677 |
rs190959228 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803747 | TAATGTAGAAACAAA[A/T]TCCAATGATATGGTT | 115677 |
rs190978737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820835 | ACATAAAGGAAAGCA[A/G]CACTTCTTTTTGGTG | 115677 |
rs191047108 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846700 | TGGTACTGAAGTACT[G/T]ACTCAAGGAATTATT | 115677 |
rs191052521 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825213 | ATACTCCCATTTAAT[A/C]CTCATAAGAACCCTT | 115677 |
rs191075241 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847710 | TGTTCATATATACTA[C/T]TGTGGAACCTCAAGA | 115677 |
rs191100285 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788546 | GGAAGCATGAAGAAT[C/G]AAAGCCCAAGCAGGG | 115677 |
rs191108543 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806531 | ATTTTCCTAATGGCC[A/G]AATGGGAAATGTCTG | 115677 |
rs191183623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803239 | TTGGAGCACTACCAA[A/G]AATATAAGTTTGGTC | 115677 |
rs191215265 | snp | A/C/T | 0.000137324 | 0.0082852 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843137 | GTTATATATTCACAT[A/C/T]TTTTTCTTCTTCTGT | 115677 |
rs191247386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848061 | ATTTTCTCTTCTCTC[C/T]TGCTCATAGGCTAAA | 115677 |
rs191261736 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800887 | TATTAACCTCAGTCT[A/G]TATCCTGTCTCTAAA | 115677 |
rs191334322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796817 | AGAAGGTCACACTTA[C/T]CTTCTGTCTCAGTGT | 115677 |
rs191397388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804486 | TCCTGGCACATTCTT[A/C]GCTTGTACTTGGGGA | 115677 |
rs191452271 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785685 | CAGGGGCAAAGCTGC[C/T]GCATTGAAGGGGGTC | 115677 |
rs191542826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807757 | GCCATGGGCCAGTTC[C/T]CTCTTCCTGGAACAA | 115677 |
rs191553167 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854874 | AAACCCATTCTGGAA[A/G]GAGCATATGTGTTTT | 115677 |
rs191553757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789506 | TGCCCCAATAACTCA[A/G]TTAACTCCCACTGGG | 115677 |
rs191632205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860281 | CACAGGCTATAAAGT[A/G]TAGTAATTGTGTAAT | 115677 |
rs191772218 | snp | C/G | | | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826921 | ACTGACCTGCTTCCT[C/G]TCAATAGAGATTCAT | 115677 |
rs191784375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788870 | CTGTGAGTATGTGTG[C/T]GTATACACACACACA | 115677 |
rs191797359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794655 | CACGCCCAGCCCAGC[A/G]GATGATTTTTAACAA | 115677 |
rs191906284 | snp | A/C | 0.00112627 | 0.0237038 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851086 | TCATTCTTTTCAGAG[A/C]ATTCTGGAGCTGGAG | 115677 |
rs191918822 | snp | C/G/T | 8.79592e-05 | 0.00663121 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811665 | AAGGTACAAAATGCA[C/G/T]GTTTGCAATAAATGG | 115677 |
rs191996198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797281 | TTTTTATTTTTGGTA[G/T]AGATGGGGTTTTACC | 115677 |
rs191997611 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840245 | GTACAAAACCAGATA[C/T]GTCAGCTGGGCGCGG | 115677 |
rs192068664 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847280 | TGTTAATAGCAGTCA[A/C]TTCTGGGTGGAAGAA | 115677 |
rs192083016 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806909 | GCCAGCTGTATTGCA[C/T]ATAACACTTAAAGGC | 115677 |
rs192120730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837097 | TCTTCTATAAGGGCA[A/G]TAATCCCATTCATGA | 115677 |
rs192131003 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863903 | GGATATATGATCCAA[C/T]GTGATCTTTTTTTAT | 115677 |
rs192217287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833532 | ACTTAAACCAAATTC[C/T]GTTTGCATAATTTAT | 115677 |
rs192234449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792371 | AAATTGTTTGGTGTA[A/G]TCATGTGAGTTTTGT | 115677 |
rs192261080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859823 | GCTAGACAAAACCGA[A/G]TACATTCTGTGTACA | 115677 |
rs192267919 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841032 | CTGAGGTAGACAGAT[C/T]GCTTGAGCCCAGGAG | 115677 |
rs192270916 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840387 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC | 115677 |
rs192280199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819008 | GCTTGGAGAAGGCAT[C/T]TTAAGTTGTATTAGC | 115677 |
rs192292939 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818767 | GCATGCTGAGAGAAA[A/C]TTAGAATGTAAAGGG | 115677 |
rs192307257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864710 | TGGCTTCATCTGAAT[C/T]AAGTGCAGAAAATGA | 115677 |
rs192321777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845261 | TGCCTCACCTCACCT[C/T]ATCACTTCCTGATGA | 115677 |
rs192323018 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797764 | AGATGAATCGCTGGA[C/G]TTCAGGAGTTTGAGA | 115677 |
rs192331122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858455 | ATTATATCTTGGTCC[C/T]TGAAGTGCCATGTTT | 115677 |
rs192352302 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786439 | CACTATGAGGCAAAA[G/T]GGGGGAGTTTAACTG | 115677 |
rs192377900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823590 | TTATGTCCAAATTTT[A/C]TCTTTATATGGGACA | 115677 |
rs192384751 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805609 | TTTTTGCTTTTTACA[C/T]ACTCATACAGTATCC | 115677 |
rs192427878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822913 | TCCAATCATAATTTA[C/T]TTTATTGCCAACGAT | 115677 |
rs192459913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864435 | GTATTACAGGCGTGC[A/G]CCACCACACCCAGCT | 115677 |
rs192497819 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790497 | GCAATAAAGATCACA[A/G]CATCACTTCTGTGAT | 115677 |
rs192523403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829517 | GTAGAGACCAGGGAT[C/T]GCTATGTTGGTCAGG | 115677 |
rs192532878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808889 | ATGCCTCAGAATAGC[C/T]AAATAAATTATGAAA | 115677 |
rs192615318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819671 | GCTCAGGTTCCCAAA[A/G]TGGTCATTAGGATTT | 115677 |
rs192688192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819879 | GAGTCCCCATCCTTC[C/T]CACTTTGCCAGACCC | 115677 |
rs192713544 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860632 | GCCAAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 115677 |
rs192727003 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844091 | AGGAAAAGAAATATA[A/C]CACTTACACAATCTG | 115677 |
rs192731616 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804375 | AGTCATGGGGAGGGC[A/G]GATATCCCTTCAGCC | 115677 |
rs192766537 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844728 | AGAAAAAATTAGCCG[C/G/T]GCGTGGTGGCGGGCG | 115677 |
rs192786752 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812233 | TGAGAAAACCCAAGG[A/G]GTGAATTTGGTTATA | 115677 |
rs192854957 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840466 | ACCCCGGAGGCGGAG[C/T]TTGCAGTGAGCTGAG | 115677 |
rs192863732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798631 | GGATAGGAGAGGTCA[A/G]ACAGTAAATCTAACC | 115677 |
rs192933209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822393 | GATCAATAGCCCATC[A/G]TCTCTGAATTTCATT | 115677 |
rs192933641 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785241 | GCTCTGGCCAAAGTT[C/T]CTGACCCAGAGTGCT | 115677 |
rs192970527 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790652 | AGGAGGAGCTAAGAA[C/T]TGTTCCAGAGTGGAA | 115677 |
rs192976883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831169 | CAAGAGCAAGGCACC[C/T]ACACATTAGCTGTGT | 115677 |
rs193029348 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814108 | ATATTCTATTAATCT[A/G]TGAATTTGTGGCACA | 115677 |
rs193043730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853674 | TAATGGTTTTAGTTA[C/G]GTGTCTTAGCAGTTT | 115677 |
rs193180985 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810306 | TAAACTACTGCATAA[C/G]GGTAAATGGATATGG | 115677 |
rs193189875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848659 | ATGAACCTTGCAGAC[A/T]TTATGCTAAGTGAAA | 115677 |
rs193225954 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793860 | AGAATAGTTTCTGTT[A/G]CGTAAACACAGCTGA | 115677 |
rs193227737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836530 | CATCTCACATAGAAG[A/C]GCTCATGATCACCTG | 115677 |
rs199524046 | snp | A/G | 0.00189004 | 0.0306831 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864975 | CAAAGGCATAAAACA[A/G]GACTCTGAACATACT | 115677 |
rs199524376 | in-del | -/AC | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807250 | TCCAAGATTTTCTGA[-/AC]ACACACACACACATA | 115677 |
rs199638021 | in-del | -/T | 0.040671 | 0.13668 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849365 | CTCTTTCTTCTTTTC[-/T]TTTTTTTTGAGATGG | 115677 |
rs199640388 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806642 | GACTGAAATCCCTTT[A/T]TCAGGGGAGAAAAAC | 115677 |
rs199650377 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844404 | AGTTTAAAAAAAAAA[A/T]GTTTAAAGCAGATAC | 115677 |
rs199669789 | snp | C/G | 5.13985e-05 | 0.00506918 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834322 | TGAGAAGGAGAAGCG[C/G]AAGGTAAGCTGTCAT | 115677 |
rs199677615 | snp | A/C | 0.000546788 | 0.0165256 | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168824689 | CTGGCAAGCAAGCTG[A/C]GCAAAGCATTACAGA | 115677 |
rs199693471 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834513 | CGCGCGCGCGCACAC[A/G]CACACACACACACAC | 115677 |
rs199709186 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832625 | CATTAATAAAAAGTG[-/T]TTGATGTAAGTGAAT | 115677 |
rs199715961 | in-del | -/GAAGGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790908 | AACTTATTCAGGACA[-/GAAGGA]AAAAAATCCTTGTAA | 115677 |
rs199728507 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849668 | GCCAGGCCTTGTTTT[A/T]ACAAAAAAAAAAAAA | 115677 |
rs199770470 | in-del | -/A/AAAAAAAAA/AAAAAAAACT | 0.0504744 | 0.152001 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838778 | GACTTCAGAATAAAT[-/A/AAAAAAAAA/AAAAAAAACT]AAAAAAAACTCTTTT | 115677 |
rs199794856 | in-del | -/CTT/CTTC | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845789 | TTAGTTTTTTTCTTC[-/CTT/CTTC]CTTTTTTTTTTTTTT | 115677 |
rs199810330 | snp | A/G | | | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786442 | TATGAGGCAAAATGG[A/G]GGAGTTTAACTGGTA | 115677 |
rs199840029 | in-del | -/AAACAAACA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860686 | AAAAAAAAAAAGAAA[-/AAACAAACA]GAAAAAACAACTTGA | 115677 |
rs199884925 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837298 | ATACACTTTTTTAAC[A/G]TCTTTTTTTTTTTTT | 115677 |
rs199903328 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813015 | AGTCAAAAAGAGAAA[A/C]ATTTTAAATATGAAG | 115677 |
rs199925489 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835000 | AGTAATGTTTTCAGG[-/A]AAAAATGTATACTTG | 115677 |
rs199984335 | snp | A/G | 0.000258164 | 0.0113585 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818266 | TCGCGAACTCCTCTC[A/G]CCTCAGCCTCTCAAG | 115677 |
rs199990125 | in-del | -/G | 0.0333695 | 0.124785 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850025 | GGTTCAGGCAATTCT[-/G]CCTCAACCTCCTGAG | 115677 |
rs200029447 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791749 | GATGGCCAGTGACGG[G/T]TTTTTTCATGTGTTT | 115677 |
rs200036644 | in-del | -/CGCGCGCGCGCGCGCACACACACA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834494 | CATTACTGGCGTGCG[-/CGCGCGCGCGCGCGCACACACACA]CACACACACACACAC | 115677 |
rs200081205 | snp | C/G | 0.000298181 | 0.0122066 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856757 | AAAGAGCCAGAAAGA[C/G]ACAGCAGCGTTAATG | 115677 |
rs200100891 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824768 | CTTTTTTTATTTGTT[G/T]TTTGTTTGTTTGTTT | 115677 |
rs200128824 | snp | A/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785766 | ATTTTTTTTTTTTTT[A/T]AAGACAGAGTCTCAC | 115677 |
rs200134156 | in-del | -/C | 0.406468 | 0.194981 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800921 | CTTTTAAAAAAAAAA[-/C]AAAAAAAGAGATGGG | 115677 |
rs200159581 | snp | G/T | 4.9938e-05 | 0.00499665 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831558 | CCACAAATACCATTT[G/T]TGTAAACTCAGTTTT | 115677 |
rs200171416 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818841 | TTAGCATATTAAAAA[A/T]TTTTTTTAATTTTTA | 115677 |
rs200235860 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826237 | GGGGTGTAGGGGTGT[A/G]TGTATTGTGTTACAG | 115677 |
rs200249700 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845615 | CATGTTTCCCCTACA[G/T]CCACCACTCCCCCTT | 115677 |
rs200260642 | snp | A/T | 0.000713403 | 0.0188731 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831511 | GCAAATCTTGTCATT[A/T]GCAACTGGAATCAGC | 115677 |
rs200361405 | snp | A/G | 0.000382979 | 0.0138327 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831560 | ACAAATACCATTTGT[A/G]TAAACTCAGTTTTTA | 115677 |
rs200383747 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849670 | CAGGCCTTGTTTTTA[A/C]AAAAAAAAAAAAAAA | 115677 |
rs200505904 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859660 | TTAAGGAGACTGGTT[-/G]TAATTTCTTGATTGG | 115677 |
rs200524713 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794425 | GGCACGATCTCAGCT[C/G]ACTGCAAGCTCCGCC | 115677 |
rs200533762 | snp | A/C | 0.294064 | 0.246086 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840541 | TCTCAAAAAAAAAAA[A/C]AAAAAAAAAACAAAA | 115677 |
rs200540361 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785329 | CTATGTCACCAAAGA[C/T]GAGTTCAAAAGGGTC | 115677 |
rs200551292 | in-del | -/A/AA | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820731 | CCAAAAAAAAAAAAA[-/A/AA]GCCCCAAATCACCTC | 115677 |
rs200698517 | snp | C/T | 0.000200304 | 0.0100056 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851367 | CTGCAATTTTATCTA[C/T]AGAAAACAAATCTGA | 115677 |
rs200809988 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855607 | CAGTTGTGTGAACAA[-/C]AAAAAAAAAAAGTAG | 115677 |
rs200813283 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834515 | CGCGCGCGCACACAC[A/G]CACACACACACACAC | 115677 |
rs200894101 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839902 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 115677 |
rs200907979 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824792 | TTTGTTTGTTTGTTT[G/T]TTGAGACAGGGTCTT | 115677 |
rs200937658 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818849 | TTAAAAAATTTTTTT[A/T]ATTTTTAATTTTTGT | 115677 |
rs201003240 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791499 | TATAATCCTTTGGGT[A/G]TATACCCAGTAATGG | 115677 |
rs201057155 | in-del | -/TGTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839922 | ATATATATATATATA[-/TGTG]TGTGTGTGTGTGTGT | 115677 |
rs201111309 | in-del | -/AGATAGAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788893 | CACACACAGATAAAA[-/AGATAGAT]AGATAGATAGATAGA | 115677 |
rs201160599 | in-del | -/AGAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863032 | ATGTGAATAAAAGAC[-/AGAC]ATACTTCCCAGATGC | 115677 |
rs201260653 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826219 | TTGCCTCCTAAGGAA[G/T]GAGGGGTGTAGGGGT | 115677 |
rs201300807 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834517 | CGCGCGCACACACAC[A/G]CACACACACACACAC | 115677 |
rs201313356 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860844 | CTTTTTTAATGAAGA[C/G]ATTAGAGAATATTGT | 115677 |
rs201323452 | snp | C/G/T | 0.000545026 | 0.0164992 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824752 | TAAGGCAAAATCAAC[C/G/T]CTTTTTTTATTTGTT | 115677 |
rs201324325 | in-del | -/AC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840546 | AAAAAAAAAAAAAAA[-/AC]AAAAACAAAAAAACA | 115677 |
rs201349358 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817558 | TGCCTTTCTTGTCCA[C/T]TTTACCTGAATTCCC | 115677 |
rs201358088 | snp | C/G | 9.93739e-05 | 0.0070482 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859588 | AACTTGAGCAAAGAC[C/G]TCAACCCAGCCATCC | 115677 |
rs201371617 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848242 | TTTGATAGGCTATTC[C/T]GTGTCTTTAATCCTT | 115677 |
rs201453794 | snp | A/C | 0.000182565 | 0.00955244 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843052 | GATGAAAATTACTAC[A/C]AAAAAAACATGGCGG | 115677 |
rs201471370 | snp | A/C/G | 4.97041e-05 | 0.00498498 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828239 | AGTTCTCCCACCCTG[A/C/G]CCTTTCTCCAACTCC | 115677 |
rs201492914 | snp | C/T | 0.000364389 | 0.013493 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828228 | CTGCATCAGTGAGTT[C/T]TCCCACCCTGGCCTT | 115677 |
rs201496382 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840563 | AAAACAAAAAAACAG[A/G]TATGTCCTGTGTAGG | 115677 |
rs201534706 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800907 | CTGTCTCTAAATTTC[-/T]TTTAAAAAAAAAACA | 115677 |
rs201594811 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848559 | TCAAATGACTATATA[-/C]CAAAAAACAAAATGT | 115677 |
rs201638736 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791747 | CTGATGGCCAGTGAC[C/G]GTTTTTTTCATGTGT | 115677 |
rs201648614 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839927 | TATATATATATGTGT[A/G]TGTGTGTGTGTGTAT | 115677 |
rs201656312 | in-del | -/C/CTC/CTTA/CTTT | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845792 | GTTTTTTTCTTCCTT[-/C/CTC/CTTA/CTTT]TTTTTTTTTTTTTTT | 115677 |
rs201670059 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837269 | TTTTTACAATACATC[-/T]TTTTTTTTTTATAAT | 115677 |
rs201763908 | snp | C/T | 0.000116251 | 0.00762312 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851286 | CATTGCAGTGCCACA[C/T]GCAGATTCACTGTGC | 115677 |
rs201804188 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791807 | CAAGTGTCTGTTCAT[A/G]TCCTTCACCCACTTT | 115677 |
rs201961674 | snp | C/T | 3.33106e-05 | 0.00408095 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824606 | GCCCAGCCCAGTACA[C/T]CCTATTTAACTAGTC | 115677 |
rs201979691 | snp | G/T | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863676 | TGCAAAGCTGTGAGT[G/T]AGTTAAACTTTTGGC | 115677 |
rs202063536 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862765 | CTCAACCTTCTTTAT[G/T]TGTCCAGTTAGAAAC | 115677 |
rs202072618 | snp | A/G | 0.00023269 | 0.0107838 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864789 | ATCGGGCTGAGGCAT[A/G]TGTTCACATCACAGA | 115677 |
rs202089194 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819046 | GCAGTAGAATGGAAA[A/G]AAAAAAATGCAAAAG | 115677 |
rs202103055 | in-del | -/ATTCTCTGGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850764 | CTGAAATTCTCTGGA[-/ATTCTCTGGA]ATCCATGATTGTGTC | 115677 |
rs202140560 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802800 | TTTAGATATTGGCTG[G/T]GGTGCAAAAGTTTGT | 115677 |
rs202204045 | snp | A/C/T | 0.00327975 | 0.0403691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802704 | TGGTTTGTGTGCCTG[A/C/T]GTGTGAGGAGGGTGG | 115677 |
rs202206148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813960 | GTAAATGTACATTTG[C/T]GGTGTCTCCTCGTCT | 115677 |
rs202229307 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834490 | AAATCATTACTGGCG[C/T]GCGCGCGCGCGCGCG | 115677 |
rs202232652 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826220 | TGCCTCCTAAGGAAT[G/T]AGGGGTGTAGGGGTG | 115677 |
rs207462645 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848177 | GAGCAGAATTTGTTT[C/T]ACGTATTTGTTATGA | 115677 |
rs207462646 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864176 | TTTCACCATGTTGGC[C/G]AGGCTGGTCTCAACC | 115677 |
rs367593396 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819466 | TGCCACTTGGAACAT[A/G]GCTTCTTATAAAGGA | 115677 |
rs367735701 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840147 | TATAACCATGACTCT[C/T]TTTGAGTCCTTGCAT | 115677 |
rs367745481 | snp | A/C | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856743 | TCCTTCTCTGATGCA[A/C]AGAGCCAGAAAGACA | 115677 |
rs367811933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859876 | AAAACACTTTTGATT[C/T]CTTCTTTCTCATCAT | 115677 |
rs367829611 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834408 | AACACAAGAGAACGG[G/T]TTGATTCCTCCTTCT | 115677 |
rs367852480 | snp | A/C | 1.6646e-05 | 0.00288491 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828394 | GCTGATATTATGCTT[A/C]TGTGTCTTTTATGTT | 115677 |
rs367977255 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804538 | TCTGCGGTTTGGGAA[C/T]AAAATAAGACAAGGA | 115677 |
rs367978473 | snp | A/G | 4.97162e-05 | 0.00498554 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856770 | GACACAGCAGCGTTA[A/G]TGGATGAGGTAAATG | 115677 |
rs367980231 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796259 | GACTCAGAACCGGGA[C/G]TTGGCCTTCGGAAGA | 115677 |
rs367985736 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838683 | TTCCTATCTATTCCC[C/T]ATGTACAAGCCAAGC | 115677 |
rs367986666 | snp | C/T | 8.31414e-05 | 0.006447 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865002 | TACTACCTTCACACT[C/T]GGTAATCAACAATAC | 115677 |
rs368016424 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802222 | CTCCAAGTCCATGAG[A/G]TCCCCAAAGGTCAAA | 115677 |
rs368021443 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837125 | TGAGGGTTCCACCCT[C/T]ATGGCCTAATCTGGT | 115677 |
rs368038198 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792498 | TCTGTCACCCAGGCT[C/G]GAGTGCAGTGGTGCG | 115677 |
rs368075219 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859195 | TCTACAATCAACACT[C/T]ATCCCCTTTCTTGTC | 115677 |
rs368106312 | snp | C/T | 4.67869e-05 | 0.00483645 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811579 | CAGTATAATAAAGTA[C/T]ACAAGAACCTAAAGG | 115677 |
rs368133789 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820918 | ATTCTGAAAGTAGAA[C/T]TGAATTCTGAGGAAG | 115677 |
rs368214644 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816979 | GGCATAATATGTAGC[A/T]TATTATTTTGAAGAA | 115677 |
rs368227954 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855268 | AGTTAAAATTAAATG[C/T]AGCCAGTGGAAGTAT | 115677 |
rs368231865 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789893 | ACTTGGAAAAACTGG[C/T]CTCATAAAAGAGCTT | 115677 |
rs368268340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830681 | TTTGGCTGTTTAAAA[A/G]CAAGGGAAAAAGTTA | 115677 |
rs368306515 | snp | C/G/T | 0.000135201 | 0.00822099 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862093 | GCCTTCCCATATTGA[C/G/T]ATTCTTAGCATGAAT | 115677 |
rs368417582 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820718 | AGGAGAAAAGCTGGC[A/C]AAAAAAAAAAAAAGC | 115677 |
rs368583308 | snp | A/G | 6.65624e-05 | 0.0057686 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811520 | TCTTCGGAGTTGCTC[A/G]TAATCTTCCTGTTCA | 115677 |
rs368599310 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858417 | AGGATGAGGAAACTT[G/T]TATTTACATTCTTCC | 115677 |
rs368622214 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812021 | AAGGGCAGAGGCAGT[C/T]TTACTCATCATTGTA | 115677 |
rs368625262 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804966 | CCCTGACTTCAAAAT[G/T]TTGGTAATACTTAAG | 115677 |
rs368625849 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849361 | TCTTTCTCTTTCTTC[C/T]TTTCTTTTTTTTGAG | 115677 |
rs368633166 | snp | C/G | 1.65792e-05 | 0.00287912 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851210 | GATCTCTCCATTTCT[C/G]GTATGCCTGGTAAGA | 115677 |
rs368633215 | snp | C/T | 5.92669e-05 | 0.00544334 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802638 | GACAAAAGCCAGACA[C/T]ATTTCAACATGAGGG | 115677 |
rs368641623 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823404 | TCTCACAGTTCTGCA[A/G]GCTGGCAGTCAGAGG | 115677 |
rs368650307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820070 | GGTGAAGTGAGAGGC[C/G]GTATCAATTTTTGAA | 115677 |
rs368664575 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837989 | TCTGGGCCTCACTCT[A/G]TTCTCTTCACCATTG | 115677 |
rs368674024 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807585 | ATCTCTTATCTGATC[A/G]CTAAATTAACAACAA | 115677 |
rs368761525 | snp | A/G | 1.67784e-05 | 0.00289636 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856657 | CCACTGAGACAGTGT[A/G]AAAGGTGACTGAGAA | 115677 |
rs368809705 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834883 | TATGTTAATATGTTA[A/T]GAACATTATAAAGCA | 115677 |
rs368861114 | snp | C/T | 0.000116004 | 0.00761504 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864853 | CATTGTGATTATACA[C/T]GAGAAAAAAGAAGGA | 115677 |
rs368976491 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847639 | TGCTTGGGCCCCAGA[C/T]AGGCTCTAAATCTGC | 115677 |
rs368978425 | snp | A/T | 3.33317e-05 | 0.00408224 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831572 | TGTGTAAACTCAGTT[A/T]TTAGAATTGAAGTGT | 115677 |
rs369097197 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849373 | TCTTTTCTTTTTTTT[-/T]GAGATGGAATCTCAC | 115677 |
rs369112517 | snp | C/T | | | intron-variant, synonymous-codon | NOSTRIN | GRCh38.p7 | 2:168846891 | AATGACAACTCATTA[C/T]ATAAAATGGACGCCT | 115677 |
rs369169893 | snp | C/G | 3.31279e-05 | 0.00406975 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859554 | GCGAACTCCTACAAA[C/G]TGTCATCAATGTTAG | 115677 |
rs369236373 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787410 | TCTTCTTCTTCATGT[C/T]GCTAACTCTTACTTG | 115677 |
rs369243630 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803459 | AGTCATCCTTCATGT[A/G]TTGATAACACAAACT | 115677 |
rs369248367 | in-del | -/GTTCCATACA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861573 | ATTGTTTGAGAAACA[-/GTTCCATACA]CAGCTAGGGATGATG | 115677 |
rs369273012 | snp | C/G | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865672 | TTAGGAAAAGAGGAA[C/G]TCAAATTGTCCCTGT | 115677 |
rs369296324 | snp | C/T | 1.6638e-05 | 0.00288422 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851329 | TGACATTGAAAAAGA[C/T]ATCCAGGCTGTAATG | 115677 |
rs369419051 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808512 | AACATGCATCCAGGT[C/T]TTTCTCTCTTGCACA | 115677 |
rs369421257 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856897 | TGACATAGAACAATC[C/T]AGTGGGGGAGCTTAT | 115677 |
rs369504304 | snp | A/T | 1.72642e-05 | 0.00293799 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834329 | GAGAAGCGGAAGGTA[A/T]GCTGTCATGGCTGGC | 115677 |
rs369509673 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860654 | CCAGCCTGGGTGACA[A/G]GGCAAGACTCTGTCT | 115677 |
rs369613152 | snp | A/G | 1.65658e-05 | 0.00287795 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828209 | AATGAAATCCACAGC[A/G]GACCTGCATCAGTGA | 115677 |
rs369643844 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797607 | CCTAGAGATACAAAA[A/C]TAACATGTCATCATC | 115677 |
rs369677808 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824950 | TTTGTGTTGGGACAG[A/G]GTCTTACTATGTTGC | 115677 |
rs369686824 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810631 | GAATAGGCTGGCTCA[C/T]TGTATGAGCAAAGAA | 115677 |
rs369690535 | snp | A/C | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864035 | CCTGCCTCAGTCTCC[A/C]AAGCTCACTGCAACC | 115677 |
rs369711462 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855638 | AAGAAAAAAGAAAGC[A/C]AAAAAAAAAAAAAAA | 115677 |
rs369729432 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839842 | AGTGAGCTGAGATCG[C/T]ACCACTGTACTCCAG | 115677 |
rs369756784 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852111 | TCTCTTGTAAGCTAA[C/T]CTCAGAAGTGACATC | 115677 |
rs369783260 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791753 | GCCAGTGACGGTTTT[A/T]TTCATGTGTTTTTTG | 115677 |
rs369788324 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822050 | TCCTGGGGTTCCAGA[A/G]CATCTGAGTTCATCA | 115677 |
rs369809650 | snp | A/G | 6.64352e-05 | 0.00576309 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851287 | ATTGCAGTGCCACAC[A/G]CAGATTCACTGTGCC | 115677 |
rs369879274 | snp | C/T | 1.6585e-05 | 0.00287962 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864826 | TTTGTCTAACTGTAT[C/T]TTCACAGGTGACATT | 115677 |
rs369890406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788086 | TGATGTAAATAGTAA[C/T]GATGACAGCCAGGCT | 115677 |
rs369890707 | snp | C/G | 6.72653e-05 | 0.00579898 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828528 | CCTTTCTTTACTCTT[C/G]CTGTTTAAAGCAAGA | 115677 |
rs369931311 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790392 | AAGGTTAAAGTAGTG[A/T]CTCTACAGCGAAGCA | 115677 |
rs369997627 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809645 | ACTCCCTTAAACTTT[C/G]CCAGTGTGCTGTAAG | 115677 |
rs370013792 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824569 | CTCCCAAAGTGCTGG[G/T]ATTATAGGTGTGAGC | 115677 |
rs370018048 | snp | A/G | 0.000201521 | 0.0100359 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856824 | GTAGTGATGAAAAGG[A/G]TTATTTTTAGAATAC | 115677 |
rs370076071 | snp | C/G | 0.00322566 | 0.0400303 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824740 | TTGTGGCAGAGGTAA[C/G]GCAAAATCAACCCTT | 115677 |
rs370103221 | snp | A/G | 1.66793e-05 | 0.0028878 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855393 | TAAAGAGAGACGAAA[A/G]TCTTTACTAAAACCA | 115677 |
rs370137089 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833249 | AAGCCTTAAAGGACC[A/T]AATATTCATGCGTCA | 115677 |
rs370163673 | snp | C/G | 1.66001e-05 | 0.00288094 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864982 | ATAAAACAAGACTCT[C/G]AACATACTACCTTCA | 115677 |
rs370167691 | snp | A/G | 0.00086723 | 0.0208054 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828379 | AAAGTAGATGTAAAC[A/G]CTGATATTATGCTTA | 115677 |
rs370236806 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815443 | CCTGCATCCTCAGAG[C/G]TAATGTTTAAACAGG | 115677 |
rs370309180 | snp | C/T | 0.00111244 | 0.023558 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850812 | TTCCTTTTCTTCTTT[C/T]CTCCCCCTTCCTCAT | 115677 |
rs370361334 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825281 | GAGACAGAAAGTTCA[A/G]GATACTTCCCCCAAT | 115677 |
rs370395080 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849501 | GCTGGGACGACAGGC[A/G]CCCGCCACCAGGCCT | 115677 |
rs370465249 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831826 | CATTGCCCCATTTTA[C/T]AGATTGGGCAATGGA | 115677 |
rs370492927 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818418 | ACCTCGGCCTCTGGA[G/T]TAGATGGGATTAGAG | 115677 |
rs370537033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823294 | ATGCTAGGATTACAG[A/G]CGTGAGCCACCGCGC | 115677 |
rs370549954 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788400 | GGAATCACTGTGGCC[C/T]GGAGTGGAATGATGG | 115677 |
rs370554122 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865347 | GTCTTTTTCCTCTGG[A/G]TTTGGGTGGCAACAG | 115677 |
rs370560850 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789117 | TGGGCAGGGAAAGCA[A/G]AGGCTGGGTGTGGAA | 115677 |
rs370562834 | snp | A/G | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860845 | TTTTTTAATGAAGAG[A/G]TTAGAGAATATTGTG | 115677 |
rs370567089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823207 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 115677 |
rs370572321 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796937 | AGTCACTCTCTCAGT[A/G]TTTAATTCAATCAAA | 115677 |
rs370574354 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819176 | CTCTACTCCCCTTGC[A/T]TGTGGTACTTTTTCA | 115677 |
rs370638504 | snp | C/T | 0.000601504 | 0.0173318 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860784 | TATGACTTTTTATGT[C/T]ATTTGAACAGGAGCA | 115677 |
rs370703225 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822695 | ATTTTAGCTATAGAT[A/G]GGTCTGTAAATAGGA | 115677 |
rs370817862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863921 | GATCTTTTTTTATTT[C/T]TTTTTTTGAGGCAGA | 115677 |
rs370885856 | snp | C/G | 1.74491e-05 | 0.00295368 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855486 | ATCTCTTTGAATGGC[C/G]AGAAAAGGGACCATA | 115677 |
rs370919293 | in-del | -/GCC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855636 | AGAAGAAAAAAGAAA[-/GCC]AAAAAAAAAAAAAAA | 115677 |
rs370929690 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796238 | CAAGGACTAGGCGTC[A/G]TCCAGGACTCAGAAC | 115677 |
rs370932753 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803470 | ATGTATTGATAACAC[A/G]AACTGTGGGGCGGCA | 115677 |
rs370966644 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830571 | ACGGCTGATCTGCTG[C/G]GTCTGTGTTCCAGGG | 115677 |
rs370967745 | snp | A/G | 0.000267348 | 0.0115587 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856664 | GACAGTGTGAAAGGT[A/G]ACTGAGAACATGATT | 115677 |
rs370978402 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795858 | TTAGTGTTTGTCCCC[A/G]CTGCTTCTGCCACAG | 115677 |
rs371030787 | snp | A/G | 0.000182004 | 0.00953776 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802608 | GTGTCCAGAATGCTG[A/G]AGCGTAGGTGAAAGG | 115677 |
rs371041874 | snp | A/T | 1.65701e-05 | 0.00287833 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864930 | CCGCTTATGTGGAGG[A/T]GTTACCTTCAAATGC | 115677 |
rs371052920 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785730 | GAGGTAGGCCACAGG[C/T]AGAAGTTATTAGCTC | 115677 |
rs371070523 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811861 | CAGGAAGTAATTCAG[C/T]TTAGGAAGGCTCAGT | 115677 |
rs371072683 | in-del | -/AAAAAGCCAAGGAAGAGAGACCT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833424 | AAGGAAGAGAGACCT[-/AAAAAGCCAAGGAAGAGAGACCT]CTCCTTTACTATCTG | 115677 |
rs371148327 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841406 | TCAGCTACCCTGGCC[-/C]AGGGAGTTTTATATT | 115677 |
rs371170589 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785091 | GTCCCAGGGGTGGGT[A/G]GTAGGTGAGGGATGA | 115677 |
rs371282752 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854545 | TAGCCTATGTGATAA[A/C]ATTCCTACATCAGCC | 115677 |
rs371338649 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848796 | CAGAGCGTAGGAAAT[A/G]AGAAGTCGTTGTTTC | 115677 |
rs371349945 | snp | A/G | | | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786444 | TGAGGCAAAATGGGG[A/G]AGTTTAACTGGTATA | 115677 |
rs371390747 | in-del | -/A | | | intron-variant, frameshift-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863419 | AGGAAGACTGAAAAA[-/A]TCACCTCAGAATGAT | 115677 |
rs371405283 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817249 | GGCACTGCCCTGGGT[A/G]ACCCAACATGCTCAG | 115677 |
rs371444854 | snp | G/T | 0.000248762 | 0.0111499 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851220 | TTTCTGGTATGCCTG[G/T]TAAGAAGGGGCAGAA | 115677 |
rs371452210 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851979 | AGGCCTCCAGTCCTC[A/G]CTGCTGTTGGTTGGA | 115677 |
rs371521336 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821248 | CTCAGAAGGGTTTAT[G/T]TGTCTAGGTATTTCA | 115677 |
rs371546572 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793517 | TTGGAAGGCTGAGGC[A/G]GGAAGATTGCTTGAG | 115677 |
rs371624174 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803984 | AGGGATGGGGTAAGT[A/G]GCAGCAAAATCTTGG | 115677 |
rs371635347 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859933 | TTTTACAGTAAAATT[C/T]CTATTAAATTGAAAT | 115677 |
rs371640994 | snp | A/G | 1.76089e-05 | 0.00296718 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855495 | AATGGCCAGAAAAGG[A/G]ACCATATGATGCTCA | 115677 |
rs371648230 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788070 | GATAAGAAAAAAAAA[-/A]TGATGTAAATAGTAA | 115677 |
rs371668130 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799673 | CGTCTAGAGTCTTTT[A/G]TGATTTAGGTCCTCT | 115677 |
rs371677313 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846035 | AGCCACAACGTGAGA[C/T]GACTTCTGTCCAGTC | 115677 |
rs371679027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839274 | AGTTTTATTCATATG[A/G]AGATCGATTTTTGAG | 115677 |
rs371723519 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834450 | CTGCAGAGATGTAGC[C/T]TGACAGAGCATAAAA | 115677 |
rs371757498 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802483 | TCTCGGGACACAAAC[A/G]GGATGAAAGTCCAGG | 115677 |
rs371793113 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794872 | GTAGCTGGGATTGCA[G/T]GTGTGCCACTGCACC | 115677 |
rs371819948 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832106 | ATGTAAAAGGGGATG[C/T]GTATATCAATTTCAT | 115677 |
rs371830801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824417 | GATTCTCGCACCTCA[A/G]CCTCCCAAGTAGCTG | 115677 |
rs371854181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824168 | TAAGGACAAAAGGAT[C/G]CTTGTAGTAAACAAA | 115677 |
rs371895459 | snp | A/G | 0.000165986 | 0.00910854 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864834 | ACTGTATTTTCACAG[A/G]TGACATTGTGATTAT | 115677 |
rs371914285 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833093 | TTTTTTTAAATAAAA[G/T]ATTTCATTTTTTTAA | 115677 |
rs371946952 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820088 | ATCAATTTTTGAAAG[C/T]CCTTTTGTTCCACTT | 115677 |
rs371977853 | snp | G/T | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862004 | CTTTGCAAGGCCTTG[G/T]ATTCTTTTCAAGCCA | 115677 |
rs371981545 | snp | C/G | 0.000165986 | 0.00910853 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811679 | ACGTTTGCAATAAAT[C/G]GTTCTTCCTCTTTAG | 115677 |
rs371996289 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865650 | GAAGGAAATAAAGGG[C/T]ATTCAATTAGGAAAA | 115677 |
rs371997626 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813067 | AATTGCTCTGGTTCC[A/G]TGACAGAGAAAGCGG | 115677 |
rs372015131 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787675 | CCTGTAGAATGAATA[C/T]GCATTTACAGAAAGA | 115677 |
rs372020042 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841267 | AAAAAAAAAAGAAAA[A/G]AAAAAGAAAGATATT | 115677 |
rs372128529 | snp | A/G | 4.97525e-05 | 0.00498736 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828459 | GGAAGCAATAAAACC[A/G]ACTTATCAAGTCCTA | 115677 |
rs372176120 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819042 | GGTGGCAGTAGAATG[A/G]AAAGAAAAAAATGCA | 115677 |
rs372189055 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832771 | TTATGAGTTTTCTTT[A/G]AAAGGAATTGTTTTG | 115677 |
rs372207684 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797440 | AAACAAAGTAAAAGA[A/G]GTGTGTGCAATGGAT | 115677 |
rs372362613 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855625 | AAAAAAAAAGTAGAA[A/G]AAAAAAGAAAGCCAA | 115677 |
rs372440183 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864075 | TGGATTCAAGTGATT[C/G]TCCTGCCTCAGTCTC | 115677 |
rs372489232 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814137 | CATTGTATACTTTTA[A/G]ACAGCATTTCTGTGT | 115677 |
rs372494457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830108 | AACCTTCTGCCTTTG[A/C]AAGCCAACTTAATAA | 115677 |
rs372497615 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844795 | GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC | 115677 |
rs372520912 | snp | A/G | 1.66269e-05 | 0.00288326 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856798 | ATGTTTGCCGAGTGC[A/G]TTTCCTAGATGTAGT | 115677 |
rs372531497 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818007 | CCCAAACTGGAAGCT[A/G]GTGCTGGTCCTAAGT | 115677 |
rs372553827 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800805 | CTGGAATGGTGGCTC[C/T]GGACAAGTTTATCTA | 115677 |
rs372577955 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864576 | AGGCGTCACCCACCA[C/T]GCCCAGCCAATCCTG | 115677 |
rs372605906 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790556 | CTGATCATGAGCAAA[C/T]ATCAGATAAGTCCAA | 115677 |
rs372606941 | snp | C/G | 0.000165986 | 0.00910854 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859556 | GAACTCCTACAAACT[C/G]TCATCAATGTTAGCA | 115677 |
rs372620014 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840552 | AAAAAAAAAAAAAAA[-/C]AAAAAAACAGATATG | 115677 |
rs372627590 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784857 | TTTCAAGTTCACTGT[A/G]TCAGTCTAATTCACA | 115677 |
rs372736892 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814984 | ATTATGAGAAGAAGG[A/C]CTTTATTGTCCTTGG | 115677 |
rs372756951 | snp | C/T | 0.000132534 | 0.00813937 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859529 | CAATTTGAAACTAGA[C/T]CTTTTGGAAGCGAAC | 115677 |
rs372804098 | in-del | -/TCTCTGGAAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850775 | GGAATTCTCTGGAAT[-/TCTCTGGAAT]CCATGATTGTGTCTC | 115677 |
rs372816885 | snp | A/T | 1.65927e-05 | 0.00288029 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859485 | TTACTAGAAATTTGC[A/T]CACATGGCCAAATGA | 115677 |
rs372867936 | snp | C/T | 1.6601e-05 | 0.00288101 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831523 | ATTAGCAACTGGAAT[C/T]AGCAAATTAAGGCAA | 115677 |
rs372892123 | snp | G/T | 0.000335944 | 0.012956 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864856 | TGTGATTATACACGA[G/T]AAAAAAGAAGGAGGA | 115677 |
rs372892417 | snp | G/T | 1.65869e-05 | 0.00287979 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828130 | AAAATGACACTCACC[G/T]TTGTTCCCCACTTTT | 115677 |
rs372928972 | in-del | -/AGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859767 | TGCAGTTAGTTAAGA[-/AGA]TAAATGTTTTTATTT | 115677 |
rs373060065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804408 | GGTTTCCAAACCCTC[C/T]AAACTCACAGAACAT | 115677 |
rs373071461 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798318 | TTCTTTGCACGCTTT[G/T]GCTACTAAAGAAACT | 115677 |
rs373115038 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812451 | TCTGTCGCTTTTCAA[A/G]TTCTTAGTTGAGATA | 115677 |
rs373128594 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825370 | CACATTCATAATAGG[C/T]CTTGGTAATGATATT | 115677 |
rs373131496 | snp | G/T | 1.65669e-05 | 0.00287805 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864895 | TGGATCTTTGAATGG[G/T]AAAAAAGGCCATTTT | 115677 |
rs373136919 | in-del | -/CCCATCTTGCA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837173 | CTATTGCATCTTCCT[-/CCCATCTTGCA]AGAGTAAAGAAAGTT | 115677 |
rs373143032 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845095 | ACAAATGAGAAAAAA[-/A]TTCCTTAATTTACAC | 115677 |
rs373158963 | multinucleotide-polymorphism | GG/TA | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845128 | TTGAACATAAGCTCC[GG/TA]GTACTCTCTTGGTTT | 115677 |
rs373174581 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814592 | AAACCCAATAAGACA[A/G]GTAAAATGGTAGTCT | 115677 |
rs373298411 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841373 | AAATTACTTGTCTGG[-/G]CATTTTGAGAGTCAG | 115677 |
rs373332938 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168801128 | GTAACCTCCAGTGAT[C/T]AAGTTCTTTGGATAA | 115677 |
rs373385556 | snp | C/T | 1.66891e-05 | 0.00288864 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855424 | AAATTATTGAGACTG[C/T]AGAGAGACATTGAAA | 115677 |
rs373388453 | snp | A/C | 8.7697e-05 | 0.00662124 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851437 | AAAAAAAGTTACATT[A/C]ATGGAGAATCTTAGG | 115677 |
rs373491717 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837383 | GGCGCGATCTCGGCT[C/T]ACTGCAAGCTCCGCC | 115677 |
rs373502252 | snp | A/C/T | 4.97165e-05 | 0.0049856 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864851 | GACATTGTGATTATA[A/C/T]ACGAGAAAAAAGAAG | 115677 |
rs373522070 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833260 | GACCAAATATTCATG[C/T]GTCACACTCTCATTT | 115677 |
rs373602118 | in-del | -/TCAA | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865447 | GAGACAGGCAATCAA[-/TCAA]GACACCAATGAGATC | 115677 |
rs373633327 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810644 | CATTGTATGAGCAAA[C/G]AACAGCACAGCCCTC | 115677 |
rs373698988 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789315 | GTATAAAGGAAAGAG[A/G]TTTAATAGGCTCACA | 115677 |
rs373747188 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786285 | ACACTGTTACAATCA[C/T]TATTTCTCTAAAACA | 115677 |
rs374098000 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858820 | TAATGGTGAGGAGGG[A/G]GCTGGATAAGCAAGA | 115677 |
rs374123020 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863060 | AGATGCCACCTAGAA[A/C]CCATGGATGCAGCAT | 115677 |
rs374159005 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837056 | TCTCACGTGGTGGAA[A/G]GAGAGCAAGGAAGCT | 115677 |
rs374191766 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834501 | GGCGTGCGCGCGCGC[A/G]CGCGCGCACACACAC | 115677 |
rs374205635 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852165 | GCAAGTCAGTAAGTG[C/T]AGCCCATACTCAAAG | 115677 |
rs374255143 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789654 | GCCCAGATTCAAAAA[A/G]AGGGTATGAAGTGGA | 115677 |
rs374315449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807128 | TTGCAAACTGTGCTC[C/T]ATGGAACCCTTTCAG | 115677 |
rs374331592 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809722 | GATAATAATAAATAT[A/G]TTATTATATTATTTT | 115677 |
rs374339670 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790880 | TTAGAAGGTGAAGGA[A/G]CATTAGATTGGCAAC | 115677 |
rs374345539 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807733 | GCTGGGAGCGAGGTA[C/T]GAGGCAAAGCCATGG | 115677 |
rs374357251 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794370 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 115677 |
rs374461718 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802482 | TTCTCGGGACACAAA[C/T]GGGATGAAAGTCCAG | 115677 |
rs374464764 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824919 | TAGAGTAGCTGGGAC[C/T]ATGCCCTAAATTTGT | 115677 |
rs374523048 | snp | A/G | 3.35576e-05 | 0.00409606 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842980 | ATGTGTGACATTGAT[A/G]TTTTACATTAGCTCC | 115677 |
rs374587949 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826354 | CATTAGAGAATTTTT[A/T]TCCATACCGAAATCT | 115677 |
rs374594222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840650 | AGTGAATGGTATTAA[C/T]GTTCAACATTTTGGA | 115677 |
rs374596064 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819647 | TCCTTCTGTCTTGCA[-/G]AGTAATTTGCTCAGG | 115677 |
rs374610147 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811967 | CATTATTGTACTTTT[C/G]ACACCGACAGCAATT | 115677 |
rs374610331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791813 | TCTGTTCATATCCTT[C/T]ACCCACTTTTTGATG | 115677 |
rs374610428 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831939 | GGGTCACTGCTCTTA[A/G]TCATTCCATTATACT | 115677 |
rs374631257 | snp | C/T | 3.94104e-05 | 0.00443888 | utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802640 | CAAAAGCCAGACACA[C/T]TTCAACATGAGGGAC | 115677 |
rs374692977 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802485 | TCGGGACACAAACGG[G/T]ATGAAAGTCCAGGGC | 115677 |
rs374706495 | snp | A/C | 0.000327946 | 0.012801 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828112 | CACATCCTATTTCCT[A/C]GGAAAATGACACTCA | 115677 |
rs374713685 | snp | A/C | 0.000163987 | 0.00905353 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851231 | CCTGGTAAGAAGGGG[A/C]AGAAACCTTTCTTCG | 115677 |
rs374763841 | snp | A/C | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865496 | GTAGGATATCTCTGA[A/C]AAACCCACAGCCAAT | 115677 |
rs374784197 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824559 | CTGCCTTGGCCTCCC[A/T]AAGTGCTGGGATTAT | 115677 |
rs374847931 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816534 | GTCCCTGCATTTGCA[C/T]AGGCTGTATTGCCTG | 115677 |
rs374849871 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848566 | ACTATATACCAAAAA[-/A]CAAAATGTGGTATAT | 115677 |
rs374879161 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795812 | TTACCTTAGATGCTA[C/T]AAATTAGGCTGGCTA | 115677 |
rs374896189 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791107 | TTAACTCATCATTTA[A/T]CATTAGGTATATCTC | 115677 |
rs374903790 | snp | C/G/T | 8.92553e-05 | 0.00667987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834349 | TCATGGCTGGCTGGG[C/G/T]GCATGTGCCATAGAG | 115677 |
rs374918545 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, missense | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865394 | GAGGGGGTCAAGCAG[A/G]GCCTGGGAGATGAGG | 115677 |
rs374949234 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828276 | AATCAAATATTTAAA[A/G]TGGGTTTGCTACAAA | 115677 |
rs375002882 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787732 | TTGGAAAGGAAAAAT[G/T]GGTTGATTTTTACAT | 115677 |
rs375028864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812693 | GAAAATGTGGGAAGG[C/T]AAATATACGGGAAGA | 115677 |
rs375029345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817645 | AATGAATGCACACTT[C/T]AGGCTCTGAAGTTCT | 115677 |
rs375030171 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854701 | TTTTCCTGCCTGGAG[C/T]GCCCTTTGCCATCTT | 115677 |
rs375031439 | snp | A/G | 0.00144342 | 0.0268259 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864986 | AACAAGACTCTGAAC[A/G]TACTACCTTCACACT | 115677 |
rs375035599 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846643 | ACCTATATTTTTCAC[A/G]ATAATAACCATACTA | 115677 |
rs375049223 | snp | C/T | 1.82115e-05 | 0.00301751 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834182 | GTTTTCTCTTGGCAT[C/T]AGCCTCTGCTCCTTT | 115677 |
rs375053776 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799182 | GCTGCTAACCAGAGC[A/G]TATACTCAGGGCCAC | 115677 |
rs375057007 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834603 | CTCACTGTGCTGCCC[-/C]AGGCTGGCATCAAAG | 115677 |
rs375067686 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787219 | GGGCATAGCGTGAAG[C/T]AGTGAGGCAGCCTCC | 115677 |
rs375102535 | snp | C/T | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865657 | ATAAAGGGCATTCAA[C/T]TAGGAAAAGAGGAAG | 115677 |
rs375116015 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809821 | AGTAAAAATTAGAAA[C/G]CTTGATTGCCAAATA | 115677 |
rs375126825 | snp | C/T | 0.000185929 | 0.00964001 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831428 | ATTACAGCAACTAAA[C/T]AAGAAGAAAGCAAAG | 115677 |
rs375129505 | snp | A/T | 0.000167986 | 0.00916323 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862070 | AATCATTCTCAAATA[A/T]TTTAATTGCCTTCCC | 115677 |
rs375158121 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808814 | ATACAATTCCAATTA[C/G]GATCCCAACGGGGAT | 115677 |
rs375159218 | snp | C/T | 0.000163987 | 0.00905353 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851281 | CTTGGCATTGCAGTG[C/T]CACACGCAGATTCAC | 115677 |
rs375213819 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842776 | CATGTGTAAAATTGG[A/G]GGAATCATACTGGAA | 115677 |
rs375265162 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830653 | TCATTTTCATCATTA[C/T]TATTACTGTCTCTTT | 115677 |
rs375288149 | snp | A/G | 6.63978e-05 | 0.00576146 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864983 | TAAAACAAGACTCTG[A/G]ACATACTACCTTCAC | 115677 |
rs375296558 | snp | C/T | 0.000416358 | 0.0144224 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828389 | TAAACGCTGATATTA[C/T]GCTTATGTGTCTTTT | 115677 |
rs375341907 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837484 | CAGCTAATTTTTTAT[A/G]TTTTTTAGTAGAGAT | 115677 |
rs375345872 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796254 | TCCAGGACTCAGAAC[C/T]GGGAGTTGGCCTTCG | 115677 |
rs375352199 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852606 | CTCCGATATGGAGAA[A/C]AAGCCCACTGGTCAT | 115677 |
rs375398443 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808414 | CCACTCTAAATCCCT[C/T]GAATCCATCTCTCTG | 115677 |
rs375423358 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794438 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCGCA | 115677 |
rs375426895 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855632 | AAGTAGAAGAAAAAA[A/G]AAAGCCAAAAAAAAA | 115677 |
rs375463497 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828785 | CAATAGAATAATTTG[C/T]AATGATTCAAAATCT | 115677 |
rs375465210 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830228 | ACCATAAATGAGGCA[-/A]CAGTGCTGTGACAGT | 115677 |
rs375476833 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860458 | GGCGGATCACCTGAG[C/G]TCAGGAGTTCGAGAG | 115677 |
rs375485596 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847830 | GATATGGATCTCTCC[C/T]TTGCACAGTGGAATT | 115677 |
rs375549537 | snp | C/T | 1.66051e-05 | 0.00288137 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860803 | TGAACAGGAGCATAC[C/T]CATAGCTATGTGAAA | 115677 |
rs375569185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854350 | TCCTTCCTTATCAGC[A/G]AAGCCTGCATCCTCC | 115677 |
rs375578090 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812419 | TAGGTTGTAGGGGAG[-/A]AAAACATAATTTCTT | 115677 |
rs375619207 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864591 | CGCCCAGCCAATCCT[C/G]TCTTTAAGCAATTAT | 115677 |
rs375619516 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825572 | TATTAAATGAGATCA[C/T]GTGTGTGGAGAGCTT | 115677 |
rs375621894 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802135 | TTTGTTGGTTTGCAT[A/G]TTAAAGGAGTGCTCA | 115677 |
rs375630877 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834113 | TTTGGAGGATTCTAG[G/T]ATACATAATTGTTAA | 115677 |
rs375637427 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847072 | TTAAAGGGATGACTA[A/G]GTGAATAAACACGCC | 115677 |
rs375726230 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807679 | TTACAGGTGTACCTT[A/G]GACACAAATCCTCTG | 115677 |
rs375743309 | snp | A/G | 0.000115958 | 0.00761352 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859541 | AGACCTTTTGGAAGC[A/G]AACTCCTACAAACTG | 115677 |
rs375862477 | snp | A/T | 3.31307e-05 | 0.00406992 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828196 | GGGCCTCAGAGGGAA[A/T]GAAATCCACAGCGGA | 115677 |
rs375895688 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804203 | TTCTTTCAGCAGCCC[A/C]CAAGGCAACCCATAA | 115677 |
rs375905098 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829793 | CAGGTGCAGGTAAGA[C/T]GTTTGTAAGCTGTGG | 115677 |
rs375931168 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794402 | TGTTGCCCAGGCTGG[A/G]GTGCAGTGGCACGAT | 115677 |
rs376026171 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800868 | GGGAATTTGAGTTAC[A/G]TGTTATTAACCTCAG | 115677 |
rs376065024 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859821 | GAGCTAGACAAAACC[A/G]AATACATTCTGTGTA | 115677 |
rs376133966 | in-del | -/TGTGTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839922 | ATATATATATATATA[-/TGTGTG]TGTGTGTGTGTGTAT | 115677 |
rs376138797 | snp | C/G/T | 3.31347e-05 | 0.00407019 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856759 | AGAGCCAGAAAGACA[C/G/T]AGCAGCGTTAATGGA | 115677 |
rs376160330 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810341 | ACTGTTCCTGTATCC[C/T]AGGCGTTGGTTTGTT | 115677 |
rs376189832 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860940 | CAATCATTTTGGCCT[G/T]GGTCCTACTGGCAGG | 115677 |
rs376219164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860279 | AACACAGGCTATAAA[G/T]TATAGTAATTGTGTA | 115677 |
rs376270061 | snp | C/T | 1.6955e-05 | 0.00291157 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860764 | ATGATAATCGTGTTA[C/T]AAAATATGACTTTTT | 115677 |
rs376271595 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858189 | TATTAGGATCATCTG[C/G]GTCCTCTCACCTGAA | 115677 |
rs376281511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824199 | TCATCTCTTCTTTAC[A/G]TAGGCATTACATTTT | 115677 |
rs376321777 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814639 | GGCATTTCCATTGAG[A/G]GTTATGACAGACAAT | 115677 |
rs376351435 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830136 | TAAAAACCAATTACT[A/G]GTCTATATTTCGTTG | 115677 |
rs376356996 | snp | A/G | 0.000116931 | 0.00764537 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855433 | AGACTGCAGAGAGAC[A/G]TTGAAAAAGCCTCAA | 115677 |
rs376366953 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844166 | TTTATATGTGTGTGT[C/T]TGTAAACTTATACAT | 115677 |
rs376369132 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809235 | CTCTTTCCACTCTGT[G/T]ATCTTAATGCATTAT | 115677 |
rs376436936 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862211 | AAAGCTCGCATAATG[A/C]TAATAGCTAACGCTT | 115677 |
rs376450347 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830293 | CACCCCCGAAATGCT[C/T]GTCCTGTTTTTCTTC | 115677 |
rs376535739 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840404 | GCGTGGTGGCAGGCA[C/T]CTGTAGTCCCAGCTA | 115677 |
rs376539345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814432 | AGCTATCTAGAAATG[C/T]GCCTTGCCCTTATTT | 115677 |
rs376539686 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833819 | TTAAAACAATCTCAA[-/A]TCGTGGCCTAGGTTG | 115677 |
rs376580017 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808896 | AGAATAGCCAAATAA[A/G]TTATGAAAAGGAAAA | 115677 |
rs376612531 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796072 | TCCCAGACTGAAAAT[A/G]AGAGTAACTTAATCA | 115677 |
rs376620564 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827751 | TTTAAAAAGTTTTTC[A/G]TAGAGAAAAGGTCTC | 115677 |
rs376798030 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820732 | CCAAAAAAAAAAAAA[A/G]CCCCAAATCACCTCA | 115677 |
rs376814691 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862919 | TCAAGATACATTTTG[C/T]AGCCAAACGACAGGG | 115677 |
rs376834816 | in-del | -/TTTT/TTTTG/TTTTGT | 0.359787 | 0.224604 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849918 | AGTAACATTTTCTCA[-/TTTT/TTTTG/TTTTGT]TTTTTTTTTTTTTTT | 115677 |
rs376851617 | snp | C/G | 0.000165986 | 0.00910854 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864809 | CACATCACAGAGACC[C/G]ATTTGTCTAACTGTA | 115677 |
rs376870472 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784997 | TTGCAGACTGAAGAA[C/T]GGAAGCGATCTAGGT | 115677 |
rs376885516 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819045 | GGCAGTAGAATGGAA[A/G]GAAAAAAATGCAAAA | 115677 |
rs376901101 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840490 | AGCTGAGATCGTGCC[A/G]CTGCACTCCAGCCTG | 115677 |
rs376913143 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818116 | AGGACTCTGTCACCT[A/G]CTTCTTTCAAGCATG | 115677 |
rs376924869 | snp | C/T | 0.000158299 | 0.00889519 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851439 | AAAAAGTTACATTAA[C/T]GGAGAATCTTAGGTA | 115677 |
rs376970244 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850616 | TTTTTTTTTTTTTTT[-/G]TAAAAACAAGGCCTG | 115677 |
rs377037962 | snp | G/T | 1.67565e-05 | 0.00289447 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856823 | TGTAGTGATGAAAAG[G/T]GTTATTTTTAGAATA | 115677 |
rs377051699 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822965 | TTAGTGCTAATATCC[C/T]GAGATCAGTAGGACA | 115677 |
rs377061765 | in-del | -/AAAG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842097 | ACAGTTTTTACACAG[-/AAAG]GCAGGGGAAAGTGAG | 115677 |
rs377062832 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837023 | TTCAGGTTGCAGACC[A/G]GCTACTTCTCATTGC | 115677 |
rs377109673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840985 | CGGCTGGGTGCGATG[A/G]CCCACACTCATGATC | 115677 |
rs377149181 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865407 | AGAGCCTGGGAGATG[A/G]GGAACACAGATCAAT | 115677 |
rs377191064 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856916 | GGGGGAGCTTATAGG[G/T]TCAGCTTCATAAGTC | 115677 |
rs377199664 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827142 | ATGCAGATCCACCCC[C/T]TTCCTCTTCATCAAA | 115677 |
rs377203260 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856132 | CGACTGAAAGAATTT[A/C]AAAATCTCATCTGGA | 115677 |
rs377241752 | snp | C/T | 1.66593e-05 | 0.00288607 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862063 | GGGTAAGAATCATTC[C/T]CAAATATTTTAATTG | 115677 |
rs377246627 | snp | A/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859572 | TCATCAATGTTAGCA[A/G]AACTTGAGCAAAGAC | 115677 |
rs377305592 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859963 | TTTTAATATTCGTTC[A/C]GACCTAAATTATAAG | 115677 |
rs377363805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815603 | ATCCATGATTCATTG[C/T]GGACACTGTCAACAA | 115677 |
rs377429537 | snp | C/T | 0.000163986 | 0.00905352 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864980 | GCATAAAACAAGACT[C/T]TGAACATACTACCTT | 115677 |
rs377429871 | snp | C/T | 0.000383746 | 0.0138465 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828378 | GAAAGTAGATGTAAA[C/T]GCTGATATTATGCTT | 115677 |
rs377498693 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857080 | CCAGTTAAGAAAAGC[A/G]ACAGGAAACAAAGGA | 115677 |
rs377560186 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821960 | CATTTTAATTTTCAT[A/G]AAACCCTCTTTAAGT | 115677 |
rs377563077 | snp | A/G | 1.65688e-05 | 0.00287821 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864917 | GGCCATTTTCCTGCC[A/G]CTTATGTGGAGGAGT | 115677 |
rs377575031 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818305 | ACTGCAGGTGTGTGC[C/T]ACTGCTCTGGGCTAA | 115677 |
rs377604945 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853312 | GTTATGAAATTTACA[G/T]GGACCAGGGACAACA | 115677 |
rs377610432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788393 | AGGTGAGGGAATCAC[G/T]GTGGCCCGGAGTGGA | 115677 |
rs377618466 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837370 | GCTGGAGTGCAGTGG[A/C]GCGATCTCGGCTTAC | 115677 |
rs377715018 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824878 | ATCCCCCAGGCTCAG[A/G]TGATCCTCCCACCCA | 115677 |
rs377765680 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788054 | GATAAGAAAGGTAAG[A/T]GATAAGAAAAAAAAA | 115677 |
rs386391757 | in-del | -/AGAGGTAT/GAGGTAT/GGGGTGTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826221 | CCTCCTAAGGAATGA[-/AGAGGTAT/GAGGTAT/GGGGTGTG]GGGGTGTAGGGGTGT | 115677 |
rs386652532 | multinucleotide-polymorphism | AG/GA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843665 | GAAATCAAAATCATC[AG/GA]TAAGCCTATGAAACA | 115677 |
rs386652533 | multinucleotide-polymorphism | ATC/GTT | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856084 | GAGGAAGAAGCCAAC[ATC/GTT]GGGTAACTGTTAGCA | 115677 |
rs397800431 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819053 | ATGGAAAGAAAAAAA[-/A]TGCAAAAGGGCTAGA | 115677 |
rs397808755 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788257 | AAAAAAAAAAAAAAA[-/A]GATGATGATATTGAT | 115677 |
rs397824376 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818848 | TTAAAAAATTTTTTT[-/T]AATTTTTAATTTTTG | 115677 |
rs397986598 | in-del | -/T | 0 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785766 | ATTTTTTTTTTTTTT[-/T]AAGACAGAGTCTCAC | 115677 |
rs527429193 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824977 | TTGCCCAGGCTGGTC[C/T]TGAACTCCTGGGCTC | 115677 |
rs527429863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791028 | TTTAAGTTTTAGGGT[A/G]CATGTCACAATGTGC | 115677 |
rs527447805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845379 | GGCACCCACCCTTCA[A/C]GGGCTATGAGAAAAA | 115677 |
rs527542948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812846 | TTAAACTCAACAACC[C/T]GCAGCATTTTTGAGA | 115677 |
rs527581333 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820766 | TGAACAAGGACCCCT[A/T]TTTCATACCACCAAA | 115677 |
rs527602617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812288 | ACTTCTAGATAGCTC[C/T]GTAATAAGCAACTCT | 115677 |
rs527617915 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845588 | TTCCTTTCCTCCTGT[C/T]AAGATCCTCTACATG | 115677 |
rs527632746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833423 | CCAAGGAAGAGAGAC[C/T]TCTCCTTTACTATCT | 115677 |
rs527699234 | snp | G/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863924 | CTTTTTTTATTTTTT[G/T]TTTTGAGGCAGAGTC | 115677 |
rs527758063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798621 | AGGAAGATTAGGATA[A/G]GAGAGGTCAGACAGT | 115677 |
rs527758680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838415 | TGGCTAATTTTTGTA[G/T]TTTTAGTAGAGATGG | 115677 |
rs527769047 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840506 | CTGCACTCCAGCCTG[A/G]GGGACAGGGCGAGAC | 115677 |
rs527770795 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814800 | GCTGGGTGCAGTGGC[C/T]CATGCCTGTAATCCT | 115677 |
rs527812643 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865014 | ACTCGGTAATCAACA[A/G]TACAGTGTGGTTCAA | 115677 |
rs527823049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797932 | AGTATCCATGGGGCA[C/T]TGGTTTCAGGATACC | 115677 |
rs527872724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820591 | AAGATTTCTAAGGTA[C/T]TTGTCTGTAAAGAGA | 115677 |
rs527909205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826703 | CCAGAAATGTGCCTG[A/C]CTTCATTTTTTAAAA | 115677 |
rs527993858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834035 | AGCTGCTCTGATGTT[G/T]TAGGTACATTTTGAA | 115677 |
rs528036445 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787011 | TGGGATTACAGGCGT[G/T]AGCCACCACACCCGG | 115677 |
rs528047499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847727 | GTGGAACCTCAAGAG[A/G]ACAGTTTGAGGTCCT | 115677 |
rs528084154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799715 | CTAACGCCAGTCTGC[C/T]GAGGTTCAAAACGTG | 115677 |
rs528085285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854875 | AACCCATTCTGGAAA[G/T]AGCATATGTGTTTTA | 115677 |
rs528088866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807629 | CTCAACTTGCATGTG[A/C]CTGGGCATACTGGCG | 115677 |
rs528100434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847125 | TAATTAAAGTGGTAT[C/T]TTCAGAGACTAATGG | 115677 |
rs528152611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806899 | ACATCAAGAAGCCAG[C/G]TGTATTGCACATAAC | 115677 |
rs528168154 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802441 | TATCTCACACTGGCC[G/T]TCTTGACCCAGAGCA | 115677 |
rs528170940 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830272 | TTAGTTAATGGATGT[C/T]ATGAGCACCCCCGAA | 115677 |
rs528187737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854317 | AAGGTAATCTCTCAG[C/T]CGGGATCCTAATTTT | 115677 |
rs528208686 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826776 | CCATTTTAAGCATAT[A/G/T]ATTTGATCAGTTTTG | 115677 |
rs528208929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861102 | AGAAGAGTAGAGGGT[G/T]GGGAAAGTATCCTAT | 115677 |
rs528249392 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835381 | ACCGCCCCTGGCCAG[A/C]CTTCTCGATAATGTA | 115677 |
rs528279236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804493 | ACATTCTTAGCTTGT[A/C]CTTGGGGAACAATGC | 115677 |
rs528283328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788424 | ATGATGGGAGCCAAA[A/T]TGGGCATGGAGATGT | 115677 |
rs528287333 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803419 | TGAAAAGCTAAGATT[A/G]GTGACATCATAAGCA | 115677 |
rs528300610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794466 | GCACCATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 115677 |
rs528344287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794026 | CATATCTTCATAATC[C/T]GTCTATCATATCTAT | 115677 |
rs528378763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840446 | GAGGCAGGAGAATGG[C/T]GTGAACCCCGGAGGC | 115677 |
rs528478760 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822572 | ACAGACTGAAAAATG[A/C]AATGAAAACTCTTAG | 115677 |
rs528485809 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794654 | CCACGCCCAGCCCAG[C/T]GGATGATTTTTAACA | 115677 |
rs528503945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823847 | TTTGGGAGGCCTAGA[C/T]GGGTGGGTCACCTGA | 115677 |
rs528507280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822089 | GGTCTCTCCCAGCTG[A/G]CTGTTAACCAGCACT | 115677 |
rs528518912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862924 | ATACATTTTGTAGCC[A/G]AACGACAGGGACACC | 115677 |
rs528606674 | snp | C/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788941 | GATAGATAGATGATA[C/G]ATATTTCATAACTGT | 115677 |
rs528614413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800216 | GTAGATGACCTGCTT[C/T]TACATGAGTGAGGTC | 115677 |
rs528717294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809750 | TTTATTAAAATATTT[A/G]TATATTAAATATAAA | 115677 |
rs528778887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808510 | TAAACATGCATCCAG[A/G]TCTTTCTCTCTTGCA | 115677 |
rs528780537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816821 | TGGGCTTGGCACTGA[A/G]TAGGCATTCAATAGA | 115677 |
rs528794074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856570 | ACAGAGCAAGACTCC[A/G]TCTTAAAAAAAAAAA | 115677 |
rs528865824 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787201 | AAAGGCATTTGAGAC[A/C]AAGGGCATAGCGTGA | 115677 |
rs528901558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836814 | GCCTCCCAGAGGCCC[A/T]CTCTTGATTATCCCA | 115677 |
rs528938030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836287 | TTTATTGATGTCATG[C/T]AATAATAAAGAAAAA | 115677 |
rs529013104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795444 | CCATAGATCACAGCT[A/G]TAGGATGACTTGACT | 115677 |
rs529105898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864487 | GAAGGGGTTTCACCA[A/T]GTTGGTCAGGCTGGT | 115677 |
rs529112226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864112 | AGCTGGGACTACAGG[A/C]GTGTGCCACCATGCC | 115677 |
rs529117762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824011 | ACCTGGGAGGTGGAG[G/T]TTACAGTGAGCCAAG | 115677 |
rs529119106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817663 | GCTCTGAAGTTCTAG[A/T]GCTGCCATTGCTTAC | 115677 |
rs529134920 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865250 | ACCCCTGGTGTCACA[A/G]AAACAGACGGAGTCC | 115677 |
rs529193291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823352 | TGTCATAACAAAGTA[C/T]CACAGAATGAGTGGC | 115677 |
rs529261547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851767 | AAATTACCGCTCCCC[A/G]CCCCCACCAAAATAA | 115677 |
rs529300514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804357 | CCACCAAAAGTATCC[A/G]GGAGTCATGGGGAGG | 115677 |
rs529325470 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837516 | GGATTTCACCGAGTT[A/T]GCTAGGATAGTCTCG | 115677 |
rs529360820 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803779 | TATATAGATTTTTAA[A/G]AGTGAAACTTCCCCC | 115677 |
rs529424492 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811605 | AAAGGAGTTTTCTCA[A/G]AATGGAGAGAATTTC | 115677 |
rs529468127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832842 | GCCCAGGCTGATCCC[A/G]AACTCCTGGGCACAA | 115677 |
rs529468205 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824829 | TTACCTGGGTTAGAG[C/T]GCAGTGGCACAATCA | 115677 |
rs529486541 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860992 | TTAGTTTCAGAGCCA[C/T]TTTGACCTGTATCTG | 115677 |
rs529574158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837720 | CTTTCCACTAAGAGT[A/G]TTCTTGCCATCGAAA | 115677 |
rs529612117 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810903 | GACATTGTGGAGTTC[C/T]AAATCAAATGACAAA | 115677 |
rs529626261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797277 | TTATTTTTTATTTTT[A/G]GTAGAGATGGGGTTT | 115677 |
rs529671690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813044 | AGTAACTTCTATCCT[A/G]ACAGCCAAATTGCTC | 115677 |
rs529696808 | in-del | -/AAAAAAAAAAAAA | 0.175254 | 0.238565 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841236 | CCAGACCCTGTCTCC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAGA | 115677 |
rs529736256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819479 | ATGGCTTCTTATAAA[C/G]GAGCGATTCTCTCAG | 115677 |
rs529752483 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865619 | TAGAAGTTCTGGCCA[C/G]GGCAATCAGGCAGGA | 115677 |
rs529801961 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832107 | TGTAAAAGGGGATGC[A/G]TATATCAATTTCATG | 115677 |
rs529821015 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786756 | CTGCCCTAAAACCTT[C/T]TAGTAAACTTTCACT | 115677 |
rs529830716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798654 | ATCTAACCGGAAGCC[A/T]GGCTGGAAAGCAGCC | 115677 |
rs529894966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805869 | CTGCAAAAATACAGA[A/C]GGAGGCTGCATATGG | 115677 |
rs529906137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846232 | GACATATAACAAAAA[C/T]AGCCTGAATTGACTC | 115677 |
rs529931722 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798000 | TATAAAATAGTGTCA[C/T]ATTTGCATATAACCT | 115677 |
rs529940962 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826418 | TACTTCTAATTCTTT[C/T]TCTCTTTCTTTCTTT | 115677 |
rs529956082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805214 | GCTGGGCCTTTCAAC[C/T]TCAAAGAGCAAGGTC | 115677 |
rs529963010 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813692 | CATCCTTATAGAGAA[G/T]AATTTAGAATTTGAA | 115677 |
rs530010681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853416 | GCCATGTTCAAAAGA[C/T]TGTTATCTGTAATTT | 115677 |
rs530036179 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824131 | TTTTAGGATCCTCTT[A/G]GATACCCTTCAGGAT | 115677 |
rs530050141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852512 | CAAAACCTGCAGAAA[G/T]AATTCTGATAGCGTT | 115677 |
rs530050184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860468 | CTGAGGTCAGGAGTT[C/T]GAGAGCAGCCTGGCT | 115677 |
rs530066203 | in-del | -/A/AA | 0.471388 | 0.116136 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844875 | CTCCGTCTCAAAAAG[-/A/AA]AAAAAAAAAAAAAGA | 115677 |
rs530085079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834119 | GGATTCTAGGATACA[G/T]AATTGTTAAAGCTAG | 115677 |
rs530104386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793246 | AGCCTCCCCACTCTT[A/C]CTAATCCTTATCTCA | 115677 |
rs530163442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799593 | GAGAGGTGCTTTTTG[C/T]TGTGCTCCTTAGCAG | 115677 |
rs530165160 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817257 | CCTGGGTGACCCAAC[A/G]TGCTCAGGGAGTCCT | 115677 |
rs530175551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787212 | AGACAAAGGGCATAG[C/G]GTGAAGCAGTGAGGC | 115677 |
rs530200902 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794437 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCGC | 115677 |
rs530238846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792663 | TTTTGTATTTTTAGT[A/G]GAGACACAGTTTTCG | 115677 |
rs530243233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792217 | TTCAGATCTCTAGAT[A/G]CAAAATGTTTATTCT | 115677 |
rs530244899 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842528 | GCTAGATAGGACAGT[A/C]GCCAGACTCATTCTA | 115677 |
rs530250530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861818 | TCAAGGAATGAACAT[C/T]ATATAAAATTACAAA | 115677 |
rs530264793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821263 | GTGTCTAGGTATTTC[A/G]AGTGCTTGACAGCAG | 115677 |
rs530276676 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824894 | TGATCCTCCCACCCA[G/T]CCTCCCATATAGAGT | 115677 |
rs530406710 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847366 | AAAGCGCCTGGGGTG[C/T]TTAAAAGTCAGATTC | 115677 |
rs530472440 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793666 | CGTAAGTTCCTATGT[A/G]GAGAGAAAAAAGACC | 115677 |
rs530511691 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801220 | CAAGTTCTTTTCCTT[A/G]ATTGTCCCCTGACTC | 115677 |
rs530516738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856062 | TTAGTGATGTGAATA[A/C]CATAACGAGGAAGAA | 115677 |
rs530517649 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807327 | AGTCTGCTGTAGCAT[A/T]TAAGTGGGTCTGCTT | 115677 |
rs530574775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808185 | TCAACTGGTTCTACT[C/T]ATTTCTACATTGGTT | 115677 |
rs530576624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800588 | AATGGCACACATGAG[A/G]AGTTTGGGGATAGGA | 115677 |
rs530605811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815670 | ATCTACTCTACCATC[A/T]TCCTGGGTGACCTTA | 115677 |
rs530679277 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788999 | CCTCAGTAGCTCCTC[C/T]TGAGCACACCTAGCA | 115677 |
rs530685622 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822156 | TAGAGCAGAGAAATC[A/T]ATTTTTAAGTGCGAT | 115677 |
rs530775558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828568 | TTAGCCCAGAAAAGG[A/G]AAAGGTGATCTGAAA | 115677 |
rs530790248 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810050 | GGCTTTCCTGGGCCA[C/G]ATTCCAGGTGGCAGT | 115677 |
rs530901856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857147 | TGCTGTTTACAGGGA[C/T]CTGGGTCAACTTTAG | 115677 |
rs530929593 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848819 | GTTGTTTCATGGGTA[C/T]GGTTTACTTTTGCAA | 115677 |
rs530931921 | snp | C/G/T | 0.000256134 | 0.0113139 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856625 | CCCTTTGAGAGCGAC[C/G/T]GACTCCTGGCTGTGT | 115677 |
rs530940078 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802049 | CCCTGTGGGATTTAG[A/G]GGGTGGGGGAATATG | 115677 |
rs530996611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796142 | GTGGAAGTGATGTCA[C/T]GTATGGTAAACACTG | 115677 |
rs531002302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803402 | ATCCCAACACATGGG[G/T]CTGAAAAGCTAAGAT | 115677 |
rs531050478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822713 | TCTGTAAATAGGACA[C/T]GGTAAAATAGGTTTA | 115677 |
rs531099527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843894 | AGTGATGCACAAGAA[C/T]GTTTATGGGAGAATT | 115677 |
rs531250507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810668 | AGCCCTCAATCCATA[C/T]TGAATTTGGGTCCTC | 115677 |
rs531275665 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784574 | TTACACGTACTCATT[C/T]TGGTTCATTACACAG | 115677 |
rs531291552 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785614 | AAGTCAATAAATGTA[A/T]TGAGCACCAATCGTT | 115677 |
rs531318567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830547 | GCTAGATCTCAGAGT[G/T]GTTGAATAACGGCTG | 115677 |
rs531336188 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796391 | GACCCCTTAACCGCT[A/G]GACCCCAGCAGCTTG | 115677 |
rs531368238 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860731 | AGCTACAGAAGAGTT[-/AA]AATTTTCATGAATGT | 115677 |
rs531371258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851809 | AAACATGTATTATCT[A/C]ATAGTTTATGTGGGT | 115677 |
rs531399234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790581 | GTCCAAATTGAAGGA[C/T]GTTACATAAAATAAT | 115677 |
rs531421499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837397 | TTACTGCAAGCTCCG[C/G]CTTCTGGGTTCATGA | 115677 |
rs531444274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811726 | GACTGGAGGAGTGAT[C/T]ACAAGCTGTCCTACT | 115677 |
rs531510243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812156 | CATGTGTAAAGCTTT[C/T]CACTGTGCTGAAATG | 115677 |
rs531525219 | snp | A/T | 3.32657e-05 | 0.0040782 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824620 | ATCCTATTTAACTAG[A/T]CCTTTTCTAACAGGG | 115677 |
rs531538429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864493 | GTTTCACCATGTTGG[G/T]CAGGCTGGTCTCGAA | 115677 |
rs531539604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858791 | CCATGCTGGAGGTGT[A/G]GGGGAGAGAGGGATA | 115677 |
rs531545591 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785681 | AAGTCAGGGGCAAAG[C/G]TGCTGCATTGAAGGG | 115677 |
rs531626284 | snp | A/G | 1.65677e-05 | 0.00287812 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864866 | CACGAGAAAAAAGAA[A/G]GAGGATGGTGGTTTG | 115677 |
rs531648102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837826 | CATTGTTTATTTCCC[A/G]TTTCTAGAAACATTC | 115677 |
rs531658393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805081 | TTTTAACCCTACGCT[A/T]CTTAAAAATGTTATT | 115677 |
rs531664811 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852524 | AAAGAATTCTGATAG[C/T]GTTTCCCTGGGTCCT | 115677 |
rs531683279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838388 | GGGAGTACAGGCGTG[C/T]GCCATCACATCTGGC | 115677 |
rs531728046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812775 | AAGTGTTGGACTGTC[C/T]TTAGGTGGGAAAGGC | 115677 |
rs531807640 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845603 | TAAGATCCTCTACAT[C/G]TTTCCCCTACAACCA | 115677 |
rs531807698 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815309 | GATTTAGCCAGAGAA[A/G]CATAGCAGCTCCTAG | 115677 |
rs531817134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786867 | AGAGTAGCTGGGACT[A/G]CAGGCGCCCGCCATC | 115677 |
rs531824447 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837048 | CATTGCATTCTCACG[-/T]GGTGGAAAGAGAGCA | 115677 |
rs531886038 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793814 | TGTGCTCAAAGCATT[-/C]TTGAGAGATTTATAA | 115677 |
rs531927775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838673 | GTGTTGCCTGTTCCT[A/G]TCTATTCCCCATGTA | 115677 |
rs531929612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825939 | TATTTTTAGGACAGT[A/G]TTTTAGTAGACTACA | 115677 |
rs531980036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854255 | TTTATAGAGGCTATT[A/C]CCTTTGCTCTAAATC | 115677 |
rs532019614 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787624 | CTGATCCTTATCAGC[-/CA]CAGTGTCCACTACAC | 115677 |
rs532047301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832958 | AAATCCATTTTCTTT[C/T]AATATTCAGCTTTCA | 115677 |
rs532074181 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791866 | TTGTTTGAGTTCATT[A/G]TAGATTCTGGATATT | 115677 |
rs532109497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805916 | CCCACAGCCTCCCCA[G/T]TGTGCATCAGTGAGA | 115677 |
rs532138654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853616 | AGCCTTGGACTGGTA[C/T]GGGAGCTATGTTATG | 115677 |
rs532181907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820463 | TCAGCATGTCACAAA[A/G]GTAAGGCAACACCTT | 115677 |
rs532193915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813894 | TTTACAATTAAATTA[C/T]TTCCCCTTAGCCAAG | 115677 |
rs532209999 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852922 | GCTTTTTTTCTTTCA[A/C]ATAATGTAGGCAGGG | 115677 |
rs532226675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799657 | GAGAACAGCCCTTAT[C/G]CGTCTAGAGTCTTTT | 115677 |
rs532246064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819943 | TGCAACTGCACAGAT[A/G]CCTTTGGAACAGGCC | 115677 |
rs532280653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804348 | GGCTCATTGCCACCA[A/G]AAGTATCCGGGAGTC | 115677 |
rs532303898 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802319 | CACTGTCAGACCAAG[C/T]GCAAGAATTGTTGGA | 115677 |
rs532324519 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856430 | AAATACGAAAATTAG[C/T]CGGACATGGTGGCAT | 115677 |
rs532361715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821459 | TCATTTGTGACATAC[A/G]TACTGAGTGCCTGTT | 115677 |
rs532385465 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839448 | GAGGGAGCCTGTCTT[C/G]TTCCATTTTCTATTC | 115677 |
rs532408559 | snp | C/G/T | 0.000226014 | 0.0106281 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818252 | TCAGACTCCTGTGCT[C/G/T]GCGAACTCCTCTCGC | 115677 |
rs532495880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793863 | ATAGTTTCTGTTACG[G/T]AAACACAGCTGATAC | 115677 |
rs532614777 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794532 | AATTTTTTGTGTTTT[C/T]ACTAGAGACGGGGTT | 115677 |
rs532627678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816270 | TGTGCCTGTCTTTAA[C/T]GCGCCTTTCACTCTG | 115677 |
rs532672968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796156 | ATGTATGGTAAACAC[C/T]GCCATGGCACTCATG | 115677 |
rs532703360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856519 | GGCAGAGGTTGCAGT[A/G]AGCCGAGATCGCGCC | 115677 |
rs532755720 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810080 | TGATGGGCCAGAATG[A/G/T]TTCTAGCAGCTGCCT | 115677 |
rs532838784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849165 | GGCCTTGAGACATAC[C/T]CATCTTTCTTCTTCC | 115677 |
rs532855393 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820153 | AAACTTCAGAGGTAG[A/G]AAAGAGGTGTGGTTA | 115677 |
rs532899508 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822155 | TAGAGCAGAGAAATC[-/A]TATTTTTAAGTGCGA | 115677 |
rs532920825 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801377 | AGGCACATACCACCA[A/C]ATCCTAATTAAAAAA | 115677 |
rs532942534 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807644 | CCTGGGCATACTGGC[A/G]TTTGAGGTTTGAGGG | 115677 |
rs532951483 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860662 | GGTGACAGGGCAAGA[-/CT]CTGTCTAAAAAAAAA | 115677 |
rs533031737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794643 | GGCGTGAGCTACCAC[A/G]CCCAGCCCAGCGGAT | 115677 |
rs533071533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836699 | CCTCACAGAGTAAAT[A/G]GAAGTCAGCACAGCC | 115677 |
rs533090956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829564 | GACCTCAGGTGATCC[A/G]CCCATCTTGGCCTCC | 115677 |
rs533152164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823297 | CTAGGATTACAGGCG[C/T]GAGCCACCGCGCCCG | 115677 |
rs533174874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850699 | AGGTGGACCATCTGA[A/G]GTCAGGAGTTCAAGG | 115677 |
rs533178629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830283 | ATGTCATGAGCACCC[C/T]CGAAATGCTTGTCCT | 115677 |
rs533229897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789947 | GGGCACCCACAGGCC[A/G]TGGGAAATATGATGC | 115677 |
rs533258530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857248 | TAGTAAATACCAGCA[C/T]AATGCTCACAGGAGG | 115677 |
rs533293517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789640 | AAGTCATGAGCCCAG[C/T]CCAGATTCAAAAAGA | 115677 |
rs533318362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831381 | GGAATAGGTTTCAAT[C/T]GATACATTTTAGGGG | 115677 |
rs533357272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790619 | TCATCTTCAAGTCTG[C/T]CAATGGCAGGAAAGC | 115677 |
rs533364604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857829 | CTTGATAATTGTACC[C/G]AGATTGGCAATTTCA | 115677 |
rs533418688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796443 | GGTCTTCAATACCAG[C/T]GGGCCAGCTGCCCCA | 115677 |
rs533485306 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840346 | CCATCCGGGCTAACA[A/T]GGTGAAACCCCGTCT | 115677 |
rs533529015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811794 | TTGCTTGAAGAGTGA[G/T]TCTCCCCTATTGCAC | 115677 |
rs533539605 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864434 | GGTATTACAGGCGTG[C/T]GCCACCACACCCAGC | 115677 |
rs533581049 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855192 | TCAGGTCTCGAACAG[G/T]TAGAACAATGTGTGT | 115677 |
rs533610093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837466 | AGGCCCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 115677 |
rs533615136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857637 | ATAAAAATGAACAGA[C/T]ATATAGCACCAGTGT | 115677 |
rs533648721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817746 | CCTCAAGAAGGGCAT[C/T]ATTCAGGTCTTATCC | 115677 |
rs533667387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824186 | TGTAGTAAACAAATC[A/G]TCTCTTCTTTACGTA | 115677 |
rs533693307 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857935 | GGTGCTGTTGCAGAA[A/G]CAAGCCTAACACTTC | 115677 |
rs533709882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837933 | ATGGGCTCCCTTTTT[C/T]GGCCTGATCTTTATA | 115677 |
rs533747619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837556 | CTTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 115677 |
rs533831098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844420 | GTTTAAAGCAGATAC[A/T]ATTGGAGAAAGCCAT | 115677 |
rs533842156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851859 | TAGCCAGGTGTCTCT[A/G]AACCCCTCCCAAGGC | 115677 |
rs533875353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791123 | CATTAGGTATATCTC[C/T]TAATGCTATCCCTCC | 115677 |
rs533878805 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816323 | GCTTCAAAGACTCCT[A/G]TGACCTTTAGGATAA | 115677 |
rs533916382 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865217 | AATTCTAGGAGACCC[G/T]AGAGATGATCCAGTA | 115677 |
rs533922615 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839640 | AGTCTACAGCCGGGC[A/G]CAGTGGCTCAGGCCT | 115677 |
rs533955374 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808735 | CAAAAACTTACTATG[A/T]CCTTGGATAGAAAGT | 115677 |
rs533973448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833032 | GAGGCTGCAATTGCT[C/T]CCAAGAAAAAACATC | 115677 |
rs533975486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790853 | TGTTTGAAGGAAATG[A/C]ACACTAAAATATTAG | 115677 |
rs533975571 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844071 | CCTCGAAAAACATGA[C/T]GTTGAGGAAAAGAAA | 115677 |
rs534062344 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812401 | TGGTTGCATCCTGAA[-/T]TAGTAGGTTGTAGGG | 115677 |
rs534089641 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793262 | CTAATCCTTATCTCA[A/G]TTCTCTTTAGAGTTT | 115677 |
rs534132161 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851497 | AAGCAAATATCATGT[G/T]TTATCAATGAAAATG | 115677 |
rs534152218 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819173 | TCTCTCTACTCCCCT[G/T]GCATGTGGTACTTTT | 115677 |
rs534192460 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786589 | TGGGCATGCAGACAG[C/T]CCACCAGAAGGGAAG | 115677 |
rs534259741 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785994 | CTGGCCTCAAGTGAT[A/C]CACCTGCCTCGGCCT | 115677 |
rs534268698 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865817 | CACAAGCATTCTTAT[A/G]TACACCAATAACAGA | 115677 |
rs534283087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832511 | TAAACAGCCACTGAT[A/G]CCAAATAACTAGAGA | 115677 |
rs534300440 | in-del | -/GGAGTCTCGCTCTGT | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853891 | TTATTTATTTGAGAC[-/GGAGTCTCGCTCTGT]GGCCCAGGCTGGAGT | 115677 |
rs534313897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792745 | TCGGCCTCCGAAAGT[G/T]CTGGGATTATAGCCA | 115677 |
rs534326156 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791242 | GTGAGAACATGCGGT[A/G]TTTGGTTTTTTGTCC | 115677 |
rs534373757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813961 | TAAATGTACATTTGC[A/G]GTGTCTCCTCGTCTT | 115677 |
rs534379360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799050 | GTCCTGGAATTTGTG[A/T]TTCACAGAACAGTGT | 115677 |
rs534387345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805559 | TATCAAACAATCACA[A/T]AGAAATCAAGGACAA | 115677 |
rs534427866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852907 | TTACATGGGGAAAGC[A/G]CTTTTTTTCTTTCAA | 115677 |
rs534439553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813249 | GAAGAATCTATGCAT[A/G]TATCAGCCAGGCATG | 115677 |
rs534443264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799392 | TGGGAACTCAGTCTC[C/T]TCCTCCCAAAGTCCC | 115677 |
rs534502854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819591 | GCAGAAAGAGTGCAC[A/G]GTGACACTGTCCCAC | 115677 |
rs534698788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796296 | AAGGTGTGTCAAGAC[A/G]TGTCACCCATGTCAT | 115677 |
rs534709917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832796 | GTTTTGTATTTTTTT[A/T]AAAGAAATAGAGACA | 115677 |
rs534737085 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168798220 | AATGGTGCCTGACAC[A/G]TGGTATGTCCTTTAA | 115677 |
rs534738987 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807281 | ACATACACACACACA[C/G]AGAGAGAGAGAGAAC | 115677 |
rs534756600 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850641 | GGCCTGGCTAGGCGC[A/G]GTGGCTCATGCCTGT | 115677 |
rs534798139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815122 | GCCAGGCCAGAGAAT[A/G]TTTCCTTTCCAAACT | 115677 |
rs534858745 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835623 | CTGGAGCCAGAAAAT[A/G/T]TCTGTAAAATCACAT | 115677 |
rs534928332 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834952 | ATAATATTTTAAATG[A/T]TTAGCAAACCATGAT | 115677 |
rs534950093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793473 | TAAATTAGCTGGGCC[C/T]GGTGGCACACACCTT | 115677 |
rs534959423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794173 | AGATGGTGCTTCATA[A/G]GACATCCCGGAATGA | 115677 |
rs534967545 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848675 | TTATGCTAAGTGAAA[C/T]AGCCAGATGCAAAAG | 115677 |
rs535072871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816437 | ATGATCCCTGCCTCT[C/T]TCCTTACTGGGCCAC | 115677 |
rs535077015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854642 | GTCTTTATTGTTCCT[C/G]ACACATTTCCCACAG | 115677 |
rs535079753 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806043 | CATATCCCGTAATCT[A/C]TGACAGTCTGCCACA | 115677 |
rs535124985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829655 | TTCCTTTTTCTTTTT[C/T]GTTGTGTATTATTCA | 115677 |
rs535152148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822392 | AGATCAATAGCCCAT[A/C]ATCTCTGAATTTCAT | 115677 |
rs535161667 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828809 | AAAATCTTATTGTAG[A/C]AGAATTTAATCACAT | 115677 |
rs535170474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861514 | GAACTTCAGTAAAAC[C/T]AGGACATTATGGTTC | 115677 |
rs535216426 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794721 | AGTGGACAGGGTGCC[C/T]TCAGTCTCAGGGGTG | 115677 |
rs535227165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841425 | GAGTTTTATATTACT[G/T]TACACTGATTTTCCA | 115677 |
rs535227677 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788721 | CACTGCTGGAAAAGG[A/G]AGGTGTAAATATGGA | 115677 |
rs535285892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857265 | ATGCTCACAGGAGGA[C/G]CTCAAAAACTAGTAA | 115677 |
rs535327052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848785 | GCCAGGGGATGCAGA[A/G]CGTAGGAAATGAGAA | 115677 |
rs535363103 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829653 | TGTTCCTTTTTCTTT[C/T]TCGTTGTGTATTATT | 115677 |
rs535370247 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852546 | TGGGTCCTCTGCCAT[-/A]ATTTTATTCAGGATT | 115677 |
rs535373168 | snp | G/T | | | intron-variant, missense | NOSTRIN | GRCh38.p7 | 2:168846926 | ACAGTAGGGCTTCAT[G/T]CTTTCCTAGGACTCT | 115677 |
rs535387104 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822972 | TAATATCCCGAGATC[A/C]GTAGGACAGTTTTCT | 115677 |
rs535427023 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837631 | ATCTTAGTGAAAGGG[G/T]TATCTATCTGCTCTG | 115677 |
rs535504724 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859357 | GAGTTTATTCCTCCA[-/T]TTTTTTTTTCCTTCG | 115677 |
rs535611283 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842783 | AAAATTGGGGGAATC[A/T]TACTGGAAGGCCCTT | 115677 |
rs535623604 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802537 | TTTGACAAGGACTGA[C/T]GTACTCTAGGCCCTT | 115677 |
rs535717724 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859814 | ATAACAAGAGCTAGA[C/T]AAAACCGAATACATT | 115677 |
rs535758089 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823728 | AGGACTTCAACTTCT[G/T]CTTGGGAGACACAAT | 115677 |
rs535772743 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784876 | GTCTAATTCACAAAG[C/G]GCACATCTCCTTCCT | 115677 |
rs535785453 | snp | A/C | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864165 | TAGAGACGGGGTTTC[A/C]CCATGTTGGCCAGGC | 115677 |
rs535799996 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790668 | TGTTCCAGAGTGGAA[A/C]CTAAAGAAACATAGT | 115677 |
rs535821432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830778 | ACAGTAAAACTGGCA[G/T]TTAGGACTGTTACCA | 115677 |
rs535823743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837499 | ATTTTTTAGTAGAGA[C/T]GGGATTTCACCGAGT | 115677 |
rs535825059 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853079 | AGTGTAAGGAGGCAG[-/C]CCATGATGACTTCTC | 115677 |
rs535886976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812479 | ATACTCTTCTGAAAA[C/T]GAGTTAGATTAACAA | 115677 |
rs535999310 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829086 | TTTTTACAAAGATGC[C/T]TTCTACGCTTATTAG | 115677 |
rs536047679 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791973 | CTTTTGCTGTGCAGA[A/G]GCTCTTGAGTTTAAT | 115677 |
rs536054609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832555 | AGACAGGCAAACTTG[A/G]TGTTACTTCCAAAGC | 115677 |
rs536067674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838482 | AAACATCAAGTGATC[C/T]GCCCGCCTTGGCCTC | 115677 |
rs536079662 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821292 | AGTGTGCTCTAACAT[C/T]GGGGCTGAGCACCCA | 115677 |
rs536080256 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805866 | TCGCTGCAAAAATAC[A/G]GAAGGAGGCTGCATA | 115677 |
rs536141711 | snp | A/C | 9.95966e-05 | 0.00705609 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831497 | AAGTTGAAAAGACAG[A/C]AAATCTTGTCATTAG | 115677 |
rs536179433 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796717 | GCGGAATCCTACTTC[A/G]TTTCCTGCTTGTCAA | 115677 |
rs536187054 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835220 | GCTGGGACTACAGGT[G/T]TGCACCACCATGCTC | 115677 |
rs536323339 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858544 | CTTAGATTAAATACT[A/G]TCTTTAGAGACCAGA | 115677 |
rs536332235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825540 | ATAATATGTGCTCTA[C/T]TGTGTGTGTGTGGGC | 115677 |
rs536397952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858276 | TATGATCTGGTGAAG[A/G]AGCAACTATGAACCT | 115677 |
rs536437646 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786090 | AAATAAAATCTATAG[A/T]TATAAGACATTGGTA | 115677 |
rs536452320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854354 | TCCTTATCAGCGAAG[C/G]CTGCATCCTCCCCTC | 115677 |
rs536472508 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793474 | AAATTAGCTGGGCCC[A/G]GTGGCACACACCTTT | 115677 |
rs536539886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853807 | ATCTGTGTCACAGGT[A/G]AAATGAGGAAAATAA | 115677 |
rs536564261 | in-del | -/AATA | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862212 | AGCTCGCATAATGAT[-/AATA]AATAGCTAACGCTTA | 115677 |
rs536585563 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795814 | ACCTTAGATGCTACA[A/G]ATTAGGCTGGCTATT | 115677 |
rs536658341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834474 | CATAAAAGGGGATTC[C/T]AAATCATTACTGGCG | 115677 |
rs536703378 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793593 | TCCAGCCTGAGTGAC[A/C]GAGTGAGACCCTGTC | 115677 |
rs536757818 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798450 | ATGCGTACTCATGTT[G/T]TTAACTCCCCTTAGA | 115677 |
rs536809902 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816037 | TCTTCCACTGTTCTG[G/T]CAAAACTCTCTTAAA | 115677 |
rs536818654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807103 | AATAAGGGAATTAGA[C/G]TTTGGTGGCTTGCAA | 115677 |
rs536868356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862222 | AATGATAATAGCTAA[C/T]GCTTATTCTGTTTAC | 115677 |
rs537015353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841551 | CCATCTTATCAAGCT[C/G]TCCATAACTTGCAGT | 115677 |
rs537089713 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802888 | TAATTGTCATCTTTC[C/T]TTCTCATATTCTTGG | 115677 |
rs537127093 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829781 | TTGTTTCATGACCAG[A/G]TGCAGGTAAGATGTT | 115677 |
rs537149914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807855 | AGAAAGTACTGGTCT[A/G]TGAAATGACAGAAAA | 115677 |
rs537156992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799930 | TAAGTTCCTCCTATT[A/G]TGAAGTGGAAGCTCT | 115677 |
rs537162782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792861 | TATTAAACAGTCGTT[A/G]TGTATACTCTGCTGT | 115677 |
rs537298444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795753 | AAAGCTTATTTTGTG[C/T]AATTTTTACAACCAC | 115677 |
rs537330204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827920 | TATACAGATATGAAA[C/T]AGGAAATGAAAATCT | 115677 |
rs537337926 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799922 | TGGGACACTAAGTTC[C/T]TCCTATTATGAAGTG | 115677 |
rs537362375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794843 | CAAGGGATCCTCCTG[A/C]CTCAGCCTCCTGAGT | 115677 |
rs537445975 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848855 | AAAAAGTTTTAGAGA[G/T]GAATTATGGTGGTGT | 115677 |
rs537494050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808657 | AATCAAATAAGAAAG[C/T]CACAGGACCTATAAA | 115677 |
rs537495698 | snp | G/T | 0.0376037 | 0.131863 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863660 | GGGAGTTACATTTCT[G/T]TGCAAAGCTGTGAGT | 115677 |
rs537496958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823466 | TCTGTGCCTCTGTCC[C/T]GGCTCCTGATGATTT | 115677 |
rs537534026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856218 | AGAGAAAGGTAAACA[A/G]TTCATTTATCATTCA | 115677 |
rs537607648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837270 | TTTTTACAATACATC[G/T]TTTTTTTTTATAATA | 115677 |
rs537612868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844236 | TGGTGGGAATACAAC[A/G]GAACTGCCAGAAACA | 115677 |
rs537650222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843534 | TGAATAAAGTAACAT[C/T]TCAATGCTTGAGATG | 115677 |
rs537668023 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828910 | TATAAAATGAATATG[-/TA]TATATATGTATAGAA | 115677 |
rs537669742 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849244 | ATGATTGCTGGTGCT[C/G]TTTGTGGGATGCAGG | 115677 |
rs537690244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836436 | ACTCTGTCATACACC[C/T]ATGCCATCTTCACTG | 115677 |
rs537770580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852470 | ATATTCTTAATTGTA[A/G]TGTTCTAGGAACTGA | 115677 |
rs537777169 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815791 | TCACAGTATATTGGA[C/T]ATCTCCACCTGGAAG | 115677 |
rs537864213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864156 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 115677 |
rs537864942 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858808 | GGGAGAGAGGGATAA[C/T]GGTGAGGAGGGGGCT | 115677 |
rs537892451 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864240 | TCGCGGCCTCCCAAC[A/G]TGCTGGGATTACAGC | 115677 |
rs537946380 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808412 | TCCCACTCTAAATCC[C/T]TCGAATCCATCTCTC | 115677 |
rs537980140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863168 | TATTCTAAGCAGTTT[C/T]TTTAAATGAAACACG | 115677 |
rs537985872 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833855 | AAGAATGATGCAGGC[A/C]GTCTTCTGTGTTTGC | 115677 |
rs538016513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803865 | GAAGTCTTTTATCAT[A/T]TATTTTTCTCTCCTT | 115677 |
rs538169952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857476 | GGGGAGATGGTAGAA[A/G]AGGCAGGGAGGTGGG | 115677 |
rs538195145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824408 | TGCTCAAGCGATTCT[C/T]GCACCTCAGCCTCCC | 115677 |
rs538229072 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785399 | AGCTGAGGGTACTAG[A/G]TGGTACATAGAACTG | 115677 |
rs538244846 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168798169 | GATGCAGAACCCAGG[G/T]ATATGGAGAGCCAAT | 115677 |
rs538259499 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846539 | ATTCCACAAACCACA[A/T]GTCAAAATTAGTCTT | 115677 |
rs538269980 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819185 | CCTTGCATGTGGTAC[-/T]TTTTCAGCTTGAACC | 115677 |
rs538291124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790746 | AACTTAGGCAGGACA[A/G]TTGGTGGAACTCAGG | 115677 |
rs538313231 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837525 | CGAGTTAGCTAGGAT[A/G]GTCTCGATCTCCTGA | 115677 |
rs538315200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805513 | CTAAGGGAAAGAATC[C/T]AATCATAAGAAAGTA | 115677 |
rs538343773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852599 | CACTCTTCTCCGATA[C/T]GGAGAACAAGCCCAC | 115677 |
rs538356854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796703 | CCCTTGGGATTCTTG[C/T]GGAATCCTACTTCGT | 115677 |
rs538378419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813118 | ATTTCTTCTGTAAGA[A/C]AATATTGTTATCAGT | 115677 |
rs538421251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812522 | CAGAAACTTATTAAT[A/G]CATGCTATACCCATC | 115677 |
rs538437766 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811511 | GGTGCTCTATCTTCG[C/G]AGTTGCTCGTAATCT | 115677 |
rs538444026 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826382 | TCTGTGTTAGGTACT[A/G]CAGATATCCTGTTAC | 115677 |
rs538460739 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798772 | CAGAAAGTGTGAATG[A/G]CATACCTTCTTGGAG | 115677 |
rs538487599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825688 | GGAGAGAAGAAAGAT[A/G]TTGGTATACCAAAGA | 115677 |
rs538489286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819058 | AAAGAAAAAAATGCA[A/G]AAGGGCTAGAGAATT | 115677 |
rs538495071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833653 | AGGGTAGGGAGACTC[C/T]TGAGTGCTCCTTCCT | 115677 |
rs538498136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792727 | TCAGGTGATCCACCT[A/G]CCTCGGCCTCCGAAA | 115677 |
rs538549069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818434 | TAGATGGGATTAGAG[C/G]TGCAAGTCACTGCTC | 115677 |
rs538561595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798802 | GGAGATGCTTCGATC[A/G]ATCGATCGATCGATA | 115677 |
rs538581224 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792052 | TTTAGACATGAAGTC[C/T]TTGCCCATGCCTATG | 115677 |
rs538596711 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838520 | ACTGGGATTACAGGC[A/G]CGAGCCACCGTGCCC | 115677 |
rs538669587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861318 | CAGGGCTTGGACTCA[C/T]GGCCTACAAACTCCT | 115677 |
rs538677989 | in-del | -/AAGT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862738 | CATTATTAAAGAAGA[-/AAGT]AAGTCTCCAGCCTCA | 115677 |
rs538816167 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840487 | GTGAGCTGAGATCGT[A/G]CCACTGCACTCCAGC | 115677 |
rs538850707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839796 | GAGGCTGAGGCAGGC[A/G]AATCGCTTGAACCTG | 115677 |
rs538898640 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844418 | ATGTTTAAAGCAGAT[A/C]CAATTGGAGAAAGCC | 115677 |
rs538904374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833212 | CAGTAATGAAGTAGT[A/C]TATTTGGGAGACTCT | 115677 |
rs538935913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847308 | GAATTATGATTTTAA[A/G]ATGTATTTTTTGTGG | 115677 |
rs539048200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811773 | TATATTTTGGTACTC[A/G]AGAGATTGCTTGAAG | 115677 |
rs539102416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827966 | GGGAAAAAAGCAGTA[C/T]ATATAATGAGTATAG | 115677 |
rs539139090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826781 | TTAAGCATATGATTT[C/G]ATCAGTTTTGACATA | 115677 |
rs539220840 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800612 | GATAGGAGTGCCCTA[C/T]CAATCTATAATTCGT | 115677 |
rs539263155 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863451 | CCAAATAAAAAGTAG[C/G]TCTTGGATCCTGACG | 115677 |
rs539279107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856404 | ACATGATGAAACTGT[C/G]TCTCTACTAAAAATA | 115677 |
rs539308090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855253 | TGTTTTATTTTATAA[A/C]GTTAAAATTAAATGC | 115677 |
rs539309365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863081 | GATGCAGCATTTAAG[C/T]TACATCATTCACAAT | 115677 |
rs539317913 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841114 | AAAAACTAGTCCCAG[C/T]TACTTGGGAGGCTGA | 115677 |
rs539400791 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859157 | ATGGCTCACCTTCTT[C/T]GCAGACCACCAAAAA | 115677 |
rs539446523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795778 | AACCACAAAGTAATT[A/G]GTACAAACAGCATAA | 115677 |
rs539449445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789144 | GGAACATCTTTTTGG[G/T]CCAGAAAGCAAAGTA | 115677 |
rs539461831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835522 | TGTGGATTCTTTGTG[A/G]TTAAATTGTTGGTAG | 115677 |
rs539569042 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801762 | ATCTAATGATTGGCA[A/C]CTGGGACCACAGGTA | 115677 |
rs539714113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790124 | ATCGCTCTTTGCCTC[A/G]TGTGTTGAACCATCA | 115677 |
rs539735723 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805306 | AATCTTGAGAGTGTC[A/C]GAACTTATTTGAAAA | 115677 |
rs539760198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822195 | TATTGACTGGCTTCA[C/T]TGTCTCAAAATACTT | 115677 |
rs539779150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796180 | ACTCATGTGCATGCA[C/G]TGACAACAGGGAACG | 115677 |
rs539809938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843400 | GCTGTCAAAGTGAAG[C/T]GTAAATTAAGGCTTA | 115677 |
rs539847259 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847313 | TGATTTTAAAATGTA[-/T]TTTTTTGTGGGCCTC | 115677 |
rs539862212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842965 | AAAATGTGTTAGTAA[A/G]TGTGTGACATTGATG | 115677 |
rs539884138 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802427 | GAAGTCATTCTCACT[A/G]TCTCACACTGGCCGT | 115677 |
rs539905279 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787040 | GCCCCAAATTCTTTC[-/T]TTCTAAGGAGCTAAG | 115677 |
rs539945816 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810106 | TGCCTCACCAGTTCA[C/T]GGTCCTCACCCTCCT | 115677 |
rs539948314 | snp | C/T | 3.31362e-05 | 0.00407026 | stop-gained, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856749 | TCTGATGCAAAGAGC[C/T]AGAAAGACACAGCAG | 115677 |
rs540022800 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831670 | AATGTTTCCTTACCT[G/T]GTTGTTACACAGATA | 115677 |
rs540031696 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784743 | ATCTCTATCTTCCCT[A/C]TTTTTGGCGTCATAT | 115677 |
rs540166230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804543 | GGTTTGGGAACAAAA[G/T]AAGACAAGGAAATGG | 115677 |
rs540218632 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846285 | GTGAGAGATGGAAAT[A/G]GGACAGTTAGGGTCT | 115677 |
rs540283572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850452 | CCTTAAACAGAGAAT[G/T]TGTGGCCTGTCATTC | 115677 |
rs540300190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864722 | AATCAAGTGCAGAAA[A/C]TGACACTACCAAGTA | 115677 |
rs540338828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864430 | AGCTGGTATTACAGG[C/T]GTGCGCCACCACACC | 115677 |
rs540393462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823932 | AATACAAAATTAGCC[A/G]GGCATTGTGGTACGT | 115677 |
rs540421787 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812808 | AGAGAGGGGCAGAGT[A/G]TGTCCCTTTGTTTTA | 115677 |
rs540428160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831000 | TGGCTAATATGTCCA[C/T]TGTAAGATCTTGAAA | 115677 |
rs540438827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841513 | TAAGGGAGCAGATCA[C/T]TGGGGAGCAGGATGA | 115677 |
rs540442055 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789674 | TATGAAGTGGAGGTG[C/T]GGTTAATTGGGAGGC | 115677 |
rs540453586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797726 | TTCACTTCTGTAATC[C/T]CAGCACTTTGGGAGG | 115677 |
rs540494611 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845066 | GAGAGATGAAAACTT[A/C/G]GGTCAAAGAGGGGAA | 115677 |
rs540494823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790406 | GACTCTACAGCGAAG[C/T]AGCCTGGCAGACACC | 115677 |
rs540516629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804755 | AGTGGGTTGCATGAA[C/T]TTCAGTGAAAAAAAA | 115677 |
rs540532978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852174 | TAAGTGCAGCCCATA[C/T]TCAAAGGTGGGTGTG | 115677 |
rs540556214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789957 | AGGCCGTGGGAAATA[C/T]GATGCTTTCTTAATG | 115677 |
rs540661449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818551 | TTTTACAAAAGCAGG[A/G]TAGTCTAATATTGAT | 115677 |
rs540686267 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792086 | TGAATGGTATTGCCT[A/G]GGTTTTCTTCTAGGG | 115677 |
rs540686368 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786390 | AGCGTCCCAATAAGA[G/T]CTCAGGTGTTAGGTA | 115677 |
rs540702093 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839521 | GTGAATAAATGAATG[C/T]GATGTTTGTTCCAAG | 115677 |
rs540767350 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785467 | TAGTTGTATCACTTA[G/T]AAGTCATTTCTGAGG | 115677 |
rs540795440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814274 | CTGAGTCAACAATTA[C/T]GTTGGTTATGGTTGT | 115677 |
rs540899875 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836298 | CATGCAATAATAAAG[A/C]AAAAAGCATGGCAGC | 115677 |
rs540925305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804314 | GTCCTTGTCTAAAAC[G/T]TTGAAGGTCATCTGT | 115677 |
rs540932957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812562 | AGGCCTTAGTTCAAA[A/G]GTATTTCTCTCTCAA | 115677 |
rs540942137 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809440 | CTTATTTCAGGAGTA[C/T]GTACCCCACTAAACA | 115677 |
rs540965914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851716 | TGTATATCACGTGGT[A/G]CTTAAATTGGTTGTC | 115677 |
rs541005755 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784664 | AAATTCTCCATTGGC[-/T]TTTTTTTTTAATCTA | 115677 |
rs541029602 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825129 | AAACATGGCAAGTAC[A/G]TAACATCAAGCATGG | 115677 |
rs541060772 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865059 | CTCTTACCTTTACAT[A/G]TTTTTCTTTTGAAAT | 115677 |
rs541107639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799562 | CTGCTGCTGCCTCCT[C/T]ACAACCCATATCCAG | 115677 |
rs541204967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853395 | ATTTGTAAGGTTACC[A/G]TAAATGCCATGTTCA | 115677 |
rs541210994 | snp | C/T | 1.65996e-05 | 0.00288089 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860923 | AGGTAATCCCATGCC[C/T]ACAATCATTTTGGCC | 115677 |
rs541292559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831811 | TCATATGTCATTGTG[C/G]ATTGCCCCATTTTAC | 115677 |
rs541325119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834494 | CATTACTGGCGTGCG[C/T]GCGCGCGCGCGCGCA | 115677 |
rs541363330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834082 | AGAACTAAAAGTACA[C/T]ATTTTTGTTTCAGCC | 115677 |
rs541369631 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819393 | CGGAAAAGCATGGAA[A/G]TGTTTGTTTCCATTT | 115677 |
rs541408530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855883 | ATTAAATTCTGTACG[G/T]AGAAGTTAGGCATGT | 115677 |
rs541415377 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830354 | CACCACCCCACTCCA[-/CT]CTCTCACAAAATATA | 115677 |
rs541435427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847407 | CCCTAGACCTGGGAG[A/C]CTCTGAATCAATCAG | 115677 |
rs541484668 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842241 | TGGGAGTGAGAGACA[C/G]GAGGGCAGAAGAAGG | 115677 |
rs541494348 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862650 | TCTAAAGAGTGAGAT[A/C]CCCTTCTTTGTGTCA | 115677 |
rs541526185 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788205 | TGATGGTGCCACTTG[C/T]ACTCCAGCCAGAGTG | 115677 |
rs541566617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861776 | CAGTCCATACATATA[A/G]AAAGTGCATCATAAG | 115677 |
rs541655088 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854735 | TTGACTAGACAGTTA[C/T]GTCTTCTTGCCTCCT | 115677 |
rs541701404 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794509 | GGTGCCCGCCACCGC[A/G]CCTGGCTAATTTTTT | 115677 |
rs541701528 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863089 | ATTTAAGTTACATCA[G/T]TCACAATAAATTGAT | 115677 |
rs541717813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840970 | GTAAAGTTGGAGAAT[C/T]GGCTGGGTGCGATGG | 115677 |
rs541764459 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168801137 | AGTGATCAAGTTCTT[G/T]GGATAAGCAAAGAGG | 115677 |
rs541769168 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809147 | TTTTCTTACACATAA[A/T]ATAAATCCAAAAGTA | 115677 |
rs541805492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848407 | AGGCAACTAAGAAGA[C/T]TGCCATGGGGGCGTG | 115677 |
rs541869193 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822588 | AATGAAAACTCTTAG[C/G]ATCTATATTAAAAAG | 115677 |
rs541876436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816173 | CCCTTAAGCCTTTTA[C/T]TCTGACAGAGCTGTG | 115677 |
rs541892623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821876 | GCCGGAGTCAGATCA[C/T]GCAGAGCTTTGCAGG | 115677 |
rs541910047 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789842 | AGAAGCTTTCTGAAC[A/C]ATTCTGCCAGCTCTG | 115677 |
rs541913015 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812768 | GATAAGCAAGTGTTG[A/G]ACTGTCTTTAGGTGG | 115677 |
rs541934728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789468 | GACTTATTCACTGTC[A/G]TGAGAACAGCACAAG | 115677 |
rs541935960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815483 | GAAAATCAATTGTTC[A/C]TCTGTAAGGGAGTTT | 115677 |
rs541982077 | snp | A/G | 0.000106493 | 0.00729624 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802723 | TGAGGAGGGTGGAGG[A/G]TGGATTTGTATATTA | 115677 |
rs542079020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837073 | AGAGCAAGGAAGCTC[C/T]CTGGGGCCTCTTCTA | 115677 |
rs542089152 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801954 | AAGTGGTTAATGTAC[A/G]CTTTGCTCCTGATAG | 115677 |
rs542112371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864266 | ACAGCTGTCAGCCAC[C/T]GTGCCTGGCTGTGAT | 115677 |
rs542227592 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826190 | GTGAATGTCCATTAC[A/G]TTTTTGATTCGAATT | 115677 |
rs542239342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796961 | AATCAAATGAAAGCA[A/G]TTATTTATTGAACAC | 115677 |
rs542305153 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803285 | TTGTGAGGTCTCCGG[C/T]GGCAATAGCAGAGAT | 115677 |
rs542315934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803335 | GCAACTAAAATAAAG[C/G]GGGGGATATGTTTAC | 115677 |
rs542342369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829450 | CTCAGCCTCTCGAGT[A/C]GCTGACATTACAGGT | 115677 |
rs542450593 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830328 | CTGCATTGCCCCTCT[C/T]CACTGCACCCCACCA | 115677 |
rs542458708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857714 | GGTTAATCTGAGAAT[C/T]ATTTAAGGAGATAAA | 115677 |
rs542553527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863860 | TCCATCAGCTACATA[C/G]AAATAGAAAGTGAGC | 115677 |
rs542588992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790529 | TTCCTGCCAAAGATA[C/T]GAAACCTGAATCTGA | 115677 |
rs542591451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837589 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 115677 |
rs542631134 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852283 | ACCTTGGACCAGATT[A/C]TCGGAGGCTTATTTT | 115677 |
rs542666057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859365 | TTCCTCCATTTTTTT[G/T]TCCTTCGGCATTTTC | 115677 |
rs542686292 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852221 | AGGCATGGGTTCTAG[A/G]AAGTGGGAGTCACTA | 115677 |
rs542697324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843761 | ACAAGAATTATTGTA[A/C]CCCTGTAGGGGGAAT | 115677 |
rs542743020 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819248 | GAAATCATTCTAAGT[C/G]GGGTGTGCCTTGCTG | 115677 |
rs542755934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858694 | AGTGGATTCCTCCAA[C/T]GATTAGAGACTTTCT | 115677 |
rs542758453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818599 | TTACATTTTAATTAG[C/T]GCTTTATCTAAAATA | 115677 |
rs542771699 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789843 | GAAGCTTTCTGAACC[A/G]TTCTGCCAGCTCTGA | 115677 |
rs542832538 | snp | A/G | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863606 | TGATGTTGTATTAAA[A/G]TTGTCTAAGTTGTTG | 115677 |
rs542832879 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792334 | GAAAAAAATGCATTA[A/C]ATAAAACTTCTTGAG | 115677 |
rs542943261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845914 | CTACCTCTATGCTGG[A/C]GGCCACCAGTGTTTC | 115677 |
rs543002147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820385 | TGACGCCTGGCACGT[C/T]GTAAGTGCCCAGTAA | 115677 |
rs543008974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804962 | TTCACCCTGACTTCA[A/G]AATGTTGGTAATACT | 115677 |
rs543177135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807440 | TGGGATAATGAAAAT[A/G]TTCTTAGCAAATCTT | 115677 |
rs543199371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799649 | TCAGAGGAGAGAACA[A/G]CCCTTATCCGTCTAG | 115677 |
rs543260232 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840215 | TCTACAGACACATGT[A/G]GTTCATTAAACTTGG | 115677 |
rs543261170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806665 | AGAAAAACCTCATCG[C/T]GTTTTTTTCCCCAAT | 115677 |
rs543293856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838365 | CTTCCTCAGCCTCCC[A/G]AGTAGCTGGGAGTAC | 115677 |
rs543298349 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813909 | TTTCCCCTTAGCCAA[G/T]AAGCCATTTTTAAAG | 115677 |
rs543334749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845141 | CCGGGTACTCTCTTG[C/G]TTTATGCTAGATAGA | 115677 |
rs543345329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797816 | GACCCTGTCTCTACC[C/T]TGTGCCTCTGTTGCC | 115677 |
rs543350527 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853513 | AGTTAAATGATGGCA[A/G]TATACCCCATCCTGA | 115677 |
rs543364193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814403 | ATACATTGGATAGAA[A/G]GCAGATTCCCACCAG | 115677 |
rs543390884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861005 | CACTTTGACCTGTAT[C/T]TGTTTAAGGAAATTT | 115677 |
rs543431370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788323 | TTCCCTTCTCTTCCT[G/T]AACTGTTCAGTCCCT | 115677 |
rs543443462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819900 | TGCCAGACCCTCAAC[A/G]TCCCCACTCCCTATC | 115677 |
rs543461619 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787661 | GTGCCCAATAAATTC[C/T]TGTAGAATGAATATG | 115677 |
rs543508515 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847114 | GCTTATGAAATAATT[-/A]AAAGTGGTATTTTCA | 115677 |
rs543513100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800308 | TCATTTGAAGCCACT[C/G]GGTTTCTGTTTGTTA | 115677 |
rs543518177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825846 | AGAAGGCTTCTGGAG[C/T]TCAAATTTCCACTCT | 115677 |
rs543520166 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833912 | TATGCTCACTAGAAC[A/G]TTATTTTGGAGGCTT | 115677 |
rs543539424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840313 | AAACGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 115677 |
rs543560861 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822453 | AGTCTATGCCACGGA[C/G]TTAATTTGTGTGAAA | 115677 |
rs543630663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862759 | TCCAGCCTCAACCTT[A/C]TTTATGTGTCCAGTT | 115677 |
rs543648233 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821966 | AATTTTCATAAAACC[C/G]TCTTTAAGTAGGTCA | 115677 |
rs543655685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | NOSTRIN | GRCh38.p7 | 2:168846872 | TCCCACTCTAGATGA[A/G]ACGAATGACAACTCA | 115677 |
rs543732970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796235 | GGCCAAGGACTAGGC[A/G]TCGTCCAGGACTCAG | 115677 |
rs543776674 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794265 | CAAAATGAAAGAACT[C/G]GTGTTTTTCAGTAGA | 115677 |
rs543818140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849084 | CTGTAGGAATTTCAA[C/G]AGGTGAGCAAGGAGA | 115677 |
rs543838741 | in-del | -/TGTT | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862230 | AGCTAACGCTTATTC[-/TGTT]TGTTTACTGTGTGTC | 115677 |
rs543894247 | in-del | -/TAAA | 0.00795532 | 0.062565 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792332 | AAGAAAAAAATGCAT[-/TAAA]TAAAACTTCTTGAGA | 115677 |
rs543923426 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809612 | TCTTTACTGCAGGTC[G/T]TCTCACAATTTGAAA | 115677 |
rs543982290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808203 | TTCTACATTGGTTAT[A/G]AGCAGAGTTTTCTCT | 115677 |
rs544024405 | in-del | -/TTTGTTTGTTTGTTTG/TTTGTTTGTTTGTTTGTTTGT | 0.0407526 | 0.137242 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824788 | TTGTTTGTTTGTTTG[lengthTooLong]TTTTTTGAGACAGGG | 115677 |
rs544112157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788765 | GAATGAACTTAGTAG[C/T]ATTGGATTAAAATTG | 115677 |
rs544125555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850210 | GAGCCACTGTGCCCG[A/G]CCTCTAAAATGTTAA | 115677 |
rs544202768 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860024 | TAAGATGGTGCCTAA[C/T]GCAGATAATGCATCA | 115677 |
rs544245078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809407 | TAGATCAAAGGGGGA[A/G]GGAGGCTGAGAAATG | 115677 |
rs544246927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856472 | CCCAGCTACTCAAGA[A/G]GCTGAGGGAGGAGAA | 115677 |
rs544297977 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804057 | TGCAATGGACAGAAG[A/G]CAGGGAAATGGTGGG | 115677 |
rs544356946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830881 | CAGCTCATGCAAGGG[C/T]CTGTTACACATGATT | 115677 |
rs544362101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830242 | CACAGTGCTGTGACA[C/G]TTAATCACAGTGCTT | 115677 |
rs544388445 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796401 | CCGCTGGACCCCAGC[A/G]GCTTGGCTAAGTACT | 115677 |
rs544409561 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813037 | AATATGAAGTAACTT[A/C]TATCCTAACAGCCAA | 115677 |
rs544466041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804178 | AAGTCTTCAGACGTG[C/G]AGAAATGTTTTCTTT | 115677 |
rs544540552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795146 | CTTATAAAGTGTAGA[C/G]GGGACCAAGGTGGAA | 115677 |
rs544570747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864379 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGGATTCT | 115677 |
rs544645579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832745 | TTTGCTTTTTAGTTT[A/T]GCCATGGATTTTATG | 115677 |
rs544658772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823863 | GGGTGGGTCACCTGA[A/G]GTCAGGCGTTTGAGA | 115677 |
rs544684574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838060 | TCGATAAATAATACA[C/T]ACTCAATAAGTATAT | 115677 |
rs544695977 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823284 | GCCTCCCAAAATGCT[A/G]GGATTACAGGCGTGA | 115677 |
rs544727148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797045 | CAGACCATTGAACTC[A/G]TACTTTTCTTTTCTT | 115677 |
rs544758069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819848 | CAGAGGGCTAGCTCG[A/G]TGACATTTGCTGTCA | 115677 |
rs544834251 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851682 | GGCAGACATGTTTCA[A/C]TGACCTATAATTAAT | 115677 |
rs544836294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843919 | AGAATTGTTTATAAT[C/T]GCATGTGAGAAAAAA | 115677 |
rs544883313 | snp | C/G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857884 | GATGCAGTGAGGTAT[C/G/T]GCTGACCTAGTTTTT | 115677 |
rs544928505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857810 | TTTCTTGTGAAGGTA[A/G]GTACTTGATAATTGT | 115677 |
rs544995661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832077 | GAGTGGCCCAGTGAG[A/G]GGTGGGTAGTGATAT | 115677 |
rs545022954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846027 | AGCCCATTAGCCACA[A/G]CGTGAGACGACTTCT | 115677 |
rs545133070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853298 | GGTTTTTATCCAGTG[A/T]TATGAAATTTACATG | 115677 |
rs545153404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844608 | TCAGCCTGGGCGGCA[C/T]GCCTGTAATCCCAGC | 115677 |
rs545174739 | snp | C/T | 3.31235e-05 | 0.00406948 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859599 | AGACCTCAACCCAGC[C/T]ATCCTTGTAGTAATT | 115677 |
rs545180284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813456 | GTTTTTCTTTTTTCT[A/T]GATCACTCCATATCC | 115677 |
rs545239760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826665 | ACCCAGCTCCTCCAA[A/G]GGGCAAATGTCAGAT | 115677 |
rs545266036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787731 | TTTGGAAAGGAAAAA[C/T]GGGTTGATTTTTACA | 115677 |
rs545402554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798534 | CCTGGAAGGGAATCC[A/G]TTGCAGGTTTTCTTT | 115677 |
rs545423681 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844796 | AATGGCGTGAACCCG[A/G]GAGGCAGAGCTTGCA | 115677 |
rs545491369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805121 | ATAGGTTTCATGAGA[C/G]TACAAAAAGGGCTCA | 115677 |
rs545548811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834488 | CCAAATCATTACTGG[C/T]GTGCGCGCGCGCGCG | 115677 |
rs545576262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794013 | ACCTCTTCTATATCA[C/T]ATCTTCATAATCTGT | 115677 |
rs545578310 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857010 | ATTGTGTCTAAAATA[A/G]TATTCTCCAAACAGA | 115677 |
rs545724744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800412 | TTCAAACATTCCTCC[A/G]AGAAGCTCAACAAAT | 115677 |
rs545734336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792386 | GTCATGTGAGTTTTG[A/T]AAGTTTTTGAATTAG | 115677 |
rs545741674 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832330 | CATATGCACAGAAGA[C/T]TATTCTAGAACAATG | 115677 |
rs545792774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789367 | CTCATAACCATGGCC[A/G]AAGGCAAAAGGCATA | 115677 |
rs545826947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854830 | TGCTAGTTTCTTTAA[C/T]GTTATGCTTCAAGGC | 115677 |
rs545841770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816272 | TGCCTGTCTTTAACG[C/T]GCCTTTCACTCTGTA | 115677 |
rs545855438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861050 | ACCGATTAATTTGTT[A/T]GACTCTGTAGCTTTA | 115677 |
rs545863663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827107 | GGCAAAACCTCTGTA[C/T]CATTCTGATTAAGGC | 115677 |
rs545878992 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841614 | GGCAATAATTACACT[C/T]GCTAAATTTTGAGTG | 115677 |
rs545895123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820478 | GGTAAGGCAACACCT[C/T]TGTCAGGAGACCACT | 115677 |
rs545912102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794450 | TCCGCCTCCCAGGTT[C/T]GCACCATTCTCCTGC | 115677 |
rs545960844 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800964 | TGACCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 115677 |
rs545994609 | in-del | -/AAAG | 0.00835141 | 0.0640778 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843580 | CAAAAGTAGACACAT[-/AAAG]AAGGAATTGTGGCAA | 115677 |
rs546001961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848324 | AATTTTGTGAAAGCC[A/T]CAGGGGACTGCCAGC | 115677 |
rs546018942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816732 | ACCCTGCACTGTAAT[C/T]CTCTGTTCACTTGCC | 115677 |
rs546042092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840396 | TTAGCCGGGCGTGGT[A/G]GCAGGCACCTGTAGT | 115677 |
rs546066942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856537 | CCGAGATCGCGCCAC[G/T]GCACTCCAGCCTGGG | 115677 |
rs546101799 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800835 | AAAATCTCTGAGGGC[A/G]GAGAAGCCCCCTCAA | 115677 |
rs546124065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823185 | CCACACCTGGCTAAT[A/T]TTTTGTATTTTTAGT | 115677 |
rs546124319 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804437 | ATTTATTTATTTGCA[A/G]TTGTTTCATCTTAAT | 115677 |
rs546127579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816100 | TGGAGTTTGTATGCT[A/G]TACAAAGGCACATGG | 115677 |
rs546227391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835958 | AACCTTTGAAATAGT[C/T]GATATCTTCTACAAA | 115677 |
rs546280261 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825673 | ATTCCTTTATTAGGG[G/T]GAGAGAAGAAAGATA | 115677 |
rs546339028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841281 | AGAAAAAGAAAGATA[C/T]TGAATGCTTTAAATA | 115677 |
rs546384061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864014 | CTCCTGGATTCAAGT[A/G]ATTCTCCTGCCTCAG | 115677 |
rs546386976 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802182 | TCTCTCTAGGAATTA[C/G]CTAACCCTCAGAGAG | 115677 |
rs546457333 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822535 | ATAATAAATAATTCT[A/C]AAATATAATAAAAAT | 115677 |
rs546473216 | snp | A/C/G | 4.9818e-05 | 0.00499069 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856792 | AGGTAAATGTTTGCC[A/C/G]AGTGCATTTCCTAGA | 115677 |
rs546492989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863241 | TTATTTGTTTGAATT[C/G]TTGTTAATAGATTAT | 115677 |
rs546538793 | in-del | -/TCAG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861351 | AGCAGCCATCTGACT[-/TCAG]TCAGTCATTCATGCA | 115677 |
rs546603443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789704 | CTACTACTATCACAA[A/C]CAATGCCATGGAAAA | 115677 |
rs546660904 | snp | A/G | 1.66106e-05 | 0.00288184 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851303 | CAGATTCACTGTGCC[A/G]TCAGCAAGATTGACA | 115677 |
rs546724847 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784679 | TTTTTTTTTTAATCT[A/G]CCTCCGTTAATTTTT | 115677 |
rs546749506 | in-del | -/TTT | 0.00371516 | 0.0429392 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850597 | GGAATTCTTCCCAAT[-/TTT]TTTTTTTTTTTTTTT | 115677 |
rs546768062 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785359 | CCCTAGAGTTTTTAA[A/G]AGCAAAGAGTATTGT | 115677 |
rs546833621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817082 | TGTGTCTTATACTTG[A/G]TCTCTTTAATTATCT | 115677 |
rs546869284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822951 | TAGAGCTAATCTGAT[C/T]AGTGCTAATATCCCG | 115677 |
rs546907684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829617 | TGAGCCACTGCCCTC[A/G]GCCTAGAACAGTTTC | 115677 |
rs546912471 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855553 | CTGCTTTTGCTATTT[A/G]GCAGGGGTCTTCTCA | 115677 |
rs546940685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796233 | CAGGCCAAGGACTAG[G/T]CGTCGTCCAGGACTC | 115677 |
rs546941594 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812314 | ACTCTAAAGAGACCT[C/T]CAGAAGACTGTTAAA | 115677 |
rs546965010 | snp | A/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856201 | CAAATTTCATTAAGT[A/G]AAGAGAAAGGTAAAC | 115677 |
rs546982165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796480 | GGGGCTGTCCCTTTA[C/T]GGTCATCTTGCTGTG | 115677 |
rs547027128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844060 | ACATGAATTAACCTC[A/G]AAAAACATGATGTTG | 115677 |
rs547041737 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803806 | CCCCTTTAATTACTT[C/T]AATCTCAGTGTTCTC | 115677 |
rs547041992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850782 | CTCTGGAATCCATGA[G/T]TGTGTCTCAAATGCT | 115677 |
rs547047003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811475 | TGACAGTCATAGTTA[C/T]AGTAGTTTTCTGAAT | 115677 |
rs547080563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857250 | GTAAATACCAGCACA[A/G]TGCTCACAGGAGGAG | 115677 |
rs547092524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818800 | TAAAAGTCAGTGCAT[C/G]TCACTTCCTTGGTCC | 115677 |
rs547168499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858379 | GATACTGGTAGATTT[C/T]GTGTCACCCACGGAA | 115677 |
rs547211864 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831703 | TTTTTCACCAAACCA[A/G]TGGAAGTGCATGGCT | 115677 |
rs547220410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805189 | CTCTAATGGGCAAAA[C/T]AGACTGACAGCTGGG | 115677 |
rs547244166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797954 | CAGGATACCCCCTCA[C/T]ATCAAAATCCAAAGA | 115677 |
rs547254542 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845934 | ACCAGTGTTTCAGTC[C/T]GTGTCCTTTTTAGTT | 115677 |
rs547258630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845487 | GTGTAGCTGATAACT[A/G]GCTTGCCTTCTTCAA | 115677 |
rs547277321 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837470 | CCCGCCACCACACCC[A/G]GCTAATTTTTTATAT | 115677 |
rs547322921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819357 | TAGACCGGAAGCATG[A/G]AAGAGCCGTGGAAGT | 115677 |
rs547383057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838810 | TTTTTTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT | 115677 |
rs547396334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858923 | TTCTAGTTCAAGGTC[A/G]TATCAAGAACAGACA | 115677 |
rs547446086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833047 | CCCAAGAAAAAACAT[C/T]TTTTATCATTTCCCA | 115677 |
rs547446139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838729 | TCGAATCTGAGCATA[C/T]CATTCCTTTTGAAAG | 115677 |
rs547456459 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817159 | GGGGATATGGAAAAG[A/G]TGATACATTTGGATT | 115677 |
rs547483781 | snp | C/T | 4.96931e-05 | 0.00498439 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864880 | AGGAGGATGGTGGTT[C/T]GGATCTTTGAATGGG | 115677 |
rs547494871 | in-del | -/AGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814975 | TATATCTACATTATG[-/AGA]AGAAGGCCTTTATTG | 115677 |
rs547533139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838448 | TTTTGCCATGTTGGC[A/C]AGGCTGGTCTCGAAC | 115677 |
rs547546568 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788066 | AAGTGATAAGAAAAA[A/C]AAAATGATGTAAATA | 115677 |
rs547551183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832280 | TAGAGCATATCTGTA[C/T]GAGTTCTTAAGCAGA | 115677 |
rs547566052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861108 | GTAGAGGGTTGGGAA[A/G]GTATCCTATGAGAAG | 115677 |
rs547651293 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860599 | TCACTTGAACCCGGG[A/C]GGTGGAGGTTGTAGT | 115677 |
rs547731051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822675 | AGTGATATGAAGATG[C/T]CCTCATTTTAGCTAT | 115677 |
rs547755932 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820949 | AGGCTGTGACTGACA[A/G]TGTTACCTTTCCTGT | 115677 |
rs547787953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787071 | AATTGAGTTCGCTGC[A/G]GACCCATAAGGATTC | 115677 |
rs547803472 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864054 | CTCACTGCAACCTCC[A/G]TCTCCTGGATTCAAG | 115677 |
rs547834658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804680 | AGCACAGTTCATAAA[A/G]TATTAGCTTAGCTAC | 115677 |
rs547835104 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854945 | TCAAAATGTCTTCCA[C/T]TCCTGAGGCAGTCAT | 115677 |
rs547840779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793558 | AGAGGTTGCAGTGAG[C/T]CAAGATCGTGTCACT | 115677 |
rs547850334 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786600 | ACAGCCCACCAGAAG[A/G]GAAGAATCAGGAGAA | 115677 |
rs547892265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839612 | TGAGAAGTTCCTTAA[C/G]TAAGAATACAGGAGT | 115677 |
rs547902305 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799765 | GGAGAGGGAAAGAAA[G/T]ACATATACCAGCCAC | 115677 |
rs547920312 | snp | C/T | 1.96605e-05 | 0.00313526 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802696 | GCTCAGTGTGGTTTG[C/T]GTGCCTGCGTGTGAG | 115677 |
rs547922380 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854349 | CTCCTTCCTTATCAG[C/T]GAAGCCTGCATCCTC | 115677 |
rs547930971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847143 | CAGAGACTAATGGCA[C/T]GGGAAACTGTTCACA | 115677 |
rs547955190 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790324 | TGTGATGAGGAGAAA[G/T]GTGTTTGCCTAGTTT | 115677 |
rs547980423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820683 | TGCTCAAGAGAAAGC[C/T]GGCAGAAACACTGGG | 115677 |
rs547990918 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797017 | TGAGGAGCTCACTGA[A/G]TACTGTGGGAGGCAG | 115677 |
rs548022072 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832135 | ATGAGTATGTGGGGT[C/T]CACTTTTTGTGCACA | 115677 |
rs548024108 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788471 | TGCAGCTGGCAGAAT[C/G/T]GTAGCCCAAGGTGGG | 115677 |
rs548024258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813964 | ATGTACATTTGCGGT[A/G]TCTCCTCGTCTTGAG | 115677 |
rs548131972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800474 | CTGGGATGCCCTGCT[A/G]CCCTTACAACGGCCC | 115677 |
rs548183973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847777 | TACCACCTATTTTAT[A/G]TAAAAAGAACAAGAT | 115677 |
rs548233389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860413 | CAGTGGCTCATGCCT[A/G]TAATCCCAGAACTTT | 115677 |
rs548234200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807643 | GCCTGGGCATACTGG[C/T]GTTTGAGGTTTGAGG | 115677 |
rs548240078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816888 | GACTCTGCCTTGAAG[A/G]CACTCATAACGTTAA | 115677 |
rs548293099 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857461 | GGTGGGAATTGGGGT[A/G]GGGAGATGGTAGAAG | 115677 |
rs548308350 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830482 | GTCTGTTACAATGAA[A/C]CATATACTCTAAATT | 115677 |
rs548361894 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824985 | GCTGGTCTTGAACTC[C/G]TGGGCTCAAGTAATC | 115677 |
rs548403322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847600 | AAGAACTGGAAGGAA[C/T]GAATGAAGAACAAAT | 115677 |
rs548405672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827895 | CCACACCTGGCCATT[C/T]CCTCTATTTTATACA | 115677 |
rs548428030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835390 | GGCCAGCCTTCTCGA[G/T]AATGTAATTTGTTCA | 115677 |
rs548461631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809980 | ACCATTAAAAAAAAA[C/T]CATGTTTCGGATGCA | 115677 |
rs548463834 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801487 | CTCGGCCTCCCAAAG[G/T]GCTTGGATTACATGC | 115677 |
rs548569142 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851999 | TGTTGGTTGGAGATA[C/T]CATTTTCTTGCCATG | 115677 |
rs548570203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830512 | TTAACCAACTGGAAA[A/G]AAATGAAAGTGTAGC | 115677 |
rs548576494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816274 | CCTGTCTTTAACGCG[C/G]CTTTCACTCTGTAGC | 115677 |
rs548656851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829663 | TCTTTTTCGTTGTGT[A/G]TTATTCAGTAGTTAA | 115677 |
rs548659014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836892 | CAGCCTTCTATAACT[C/T]CCCCTGTCTTATAGT | 115677 |
rs548661832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822118 | CTCTTTTTCTCTCCT[C/T]TCCATCAACTGGGAC | 115677 |
rs548668919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862928 | ATTTTGTAGCCAAAC[A/G]ACAGGGACACCACAC | 115677 |
rs548696061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836339 | ATTTCCTCTTCCTAC[A/C]CCCATCAGCAGCTTC | 115677 |
rs548727689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795542 | TGTTTTATGCAAACT[A/G]ATCTATTTGGTTTCC | 115677 |
rs548744360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857966 | TTGTAAAAGAAAATA[A/G]CCTGCATTGTGTGCA | 115677 |
rs548746818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790034 | GGCCCCCAGCCAGAT[A/C]GAGTTAGCTCATTCT | 115677 |
rs548832779 | snp | A/G | 8.40626e-05 | 0.00648261 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843117 | AGAGAACTGCTACCA[A/G]GTAAGTTATATATTC | 115677 |
rs548926380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823423 | GGCAGTCAGAGGTGC[A/G]TTCTGAGGGCTGTGA | 115677 |
rs548943275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818210 | TCAGGCTGGAGTGCA[A/G]TGGTGCAATTATAGC | 115677 |
rs548971705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864491 | GGGTTTCACCATGTT[C/G]GTCAGGCTGGTCTCG | 115677 |
rs549041758 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821936 | CCTAGTAGACTTGGG[C/T]TCTCAACACATTTTA | 115677 |
rs549109679 | snp | A/G | 0.000116446 | 0.00762952 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851324 | AAGATTGACATTGAA[A/G]AAGATATCCAGGCTG | 115677 |
rs549189165 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864204 | ACCTCTTGACCTCAA[C/G]TAATCTGCCTAATCT | 115677 |
rs549205961 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785900 | GAATTACAGGTGCAT[A/G]CCACCACACCCAGCT | 115677 |
rs549210713 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858624 | GTGAAGGTCTAATGG[C/T]AGAAAGCATGGGGGA | 115677 |
rs549223182 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840727 | GAGAGAGTCCATTTT[A/G]ACAGCCTTTGTCTCT | 115677 |
rs549301377 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865258 | TGTCACAGAAACAGA[C/T]GGAGTCCAAGGTGGG | 115677 |
rs549338600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805343 | CTGTAAGATATCTTT[A/G]AAGTTCTGTTTTTGA | 115677 |
rs549357760 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810651 | TGAGCAAAGAACAGC[A/T]CAGCCCTCAATCCAT | 115677 |
rs549372277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837503 | TTTAGTAGAGATGGG[A/G]TTTCACCGAGTTAGC | 115677 |
rs549386635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796681 | CCAAGAAAGTTCTCT[A/T]AGTGGCCCCTTGGGA | 115677 |
rs549426443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804363 | AAAGTATCCGGGAGT[C/T]ATGGGGAGGGCGGAT | 115677 |
rs549430396 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848281 | AGACAGAAGGGCAGA[C/T]GGCCACATTCAAATG | 115677 |
rs549515624 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819026 | AAGTTGTATTAGCTA[C/T]GGTGGCAGTAGAATG | 115677 |
rs549533924 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786463 | TTAACTGGTATATGA[A/C]CTTCCTCTAGGAACG | 115677 |
rs549537993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814912 | TCTATTTTCATAAAC[A/G]AATTTTTTTAAATAA | 115677 |
rs549601127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832918 | TGAGCCACTACACCT[C/G]GCCTTTAAAAGGATT | 115677 |
rs549608735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819484 | TTCTTATAAAGGAGC[A/G]ATTCTCTCAGGGGAA | 115677 |
rs549612769 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865637 | CAATCAGGCAGGAGA[A/G]GGAAATAAAGGGCAT | 115677 |
rs549613928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798682 | GCCAGAGTATGAGTG[C/T]GGGTCAGAAATGTAG | 115677 |
rs549641682 | in-del | -/TTG/TTGG/TTGTTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849920 | TAACATTTTCTCATT[-/TTG/TTGG/TTGTTG]TTTTTTTTTTTTTTG | 115677 |
rs549675298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798086 | GCTATGTAAACGTTA[C/T]ATAAATAGTCATAAA | 115677 |
rs549675664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805892 | GCATATGGCATGGGT[A/G]TCACGTGGCCCACAG | 115677 |
rs549727848 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838861 | GGTGCAATCTGGGCC[A/G]ACTGCAACCTCTGCC | 115677 |
rs549730612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820759 | CTCAAAGTGAACAAG[A/G]ACCCCTTTTTCATAC | 115677 |
rs549779562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852563 | TTTTATTCAGGATTT[C/T]AAGCTCCAGATTAGG | 115677 |
rs549819103 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792333 | AGAAAAAAATGCATT[A/G]AATAAAACTTCTTGA | 115677 |
rs549973570 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849795 | CATGGCCTTGGAGTC[C/T]CCCTGAATACTCTGC | 115677 |
rs549980271 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795867 | GTCCCCACTGCTTCT[C/G]CCACAGTTTAAAGTA | 115677 |
rs550039285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821434 | GAAGTCCATTCACTT[A/T]TTCATTCATTCATTT | 115677 |
rs550051052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846245 | AACAGCCTGAATTGA[C/T]TCAAAGAGGAATTTT | 115677 |
rs550053055 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825245 | AGAGGTCTTGTTATC[C/G]CTGTTTACAGATAAG | 115677 |
rs550138347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845532 | GGCTATGATTATCTT[A/C]ATTATCAGAAGCTCT | 115677 |
rs550189302 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787907 | GTCCTTGGTCTTACA[G/T]CCAGAAAGTGGTGAT | 115677 |
rs550190633 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791490 | AGCATGATTTATAAT[-/C]CTTTGGGTATATACC | 115677 |
rs550208529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861224 | GAGGAGCTTTGTCGC[C/T]CTGTCTCCATAGCCT | 115677 |
rs550237984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834172 | AAAGAGGAGAGTTTT[C/T]TCTTGGCATCAGCCT | 115677 |
rs550279109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839279 | TATTCATATGGAGAT[C/T]GATTTTTGAGCACTT | 115677 |
rs550285420 | in-del | -/ATAAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804907 | ATCAGAAATTTTATG[-/ATAAC]ATTACAGTTGTTGCA | 115677 |
rs550289554 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788571 | GCAGGGTGATGAGGC[A/C]ATCCCTGCAGAGGGG | 115677 |
rs550321084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807718 | AATTGGCAGAGTATG[G/T]CTGGGAGCGAGGTAC | 115677 |
rs550359269 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840485 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 115677 |
rs550412854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861850 | TTTCCTTTTGAGAAA[A/T]ATTTAATATATTGAA | 115677 |
rs550532201 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802335 | GCAAGAATTGTTGGA[A/G]ACATGTTACAGCTTC | 115677 |
rs550580677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794633 | TAGGCTTACAGGCGT[A/G]AGCTACCACGCCCAG | 115677 |
rs550642545 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801310 | TGCCCAGCTTTGAAC[C/G]CCTAGACCCAAGAAA | 115677 |
rs550707225 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800599 | TGAGGAGTTTGGGGA[C/T]AGGAGTGCCCTACCA | 115677 |
rs550760599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822819 | GCCTTGTGCTGCAAA[G/T]AAAGTAATAGAAATT | 115677 |
rs550873791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802822 | AAAGTTTGTGGTTTT[A/T]CTTTGGTTCAGTTTA | 115677 |
rs550884752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828666 | GAATAATAAAAAACA[C/T]AAATCCAAGATTTAT | 115677 |
rs550918930 | snp | C/T | 0.000253068 | 0.0112459 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818265 | CTCGCGAACTCCTCT[C/T]GCCTCAGCCTCTCAA | 115677 |
rs550987060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810070 | CAGGTGGCAGTGATG[A/G]GCCAGAATGGTTCTA | 115677 |
rs551050457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817025 | AAATCACAGGAGAGA[A/C]CACTTATTCAGTACA | 115677 |
rs551136244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790097 | TCTACTTTAAGTGCT[A/T]TCTCCAAAGACATCG | 115677 |
rs551146947 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785289 | CCATCAAGCAATCCT[A/G]TGTTAGATTTCAGAC | 115677 |
rs551182202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831262 | AGGGGCTAGGCAGCT[C/G]TTGGGGTCTCTTTTA | 115677 |
rs551255738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804413 | CCAAACCCTCTAAAC[C/T]CACAGAACATTTATT | 115677 |
rs551336646 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850646 | GGCTAGGCGCGGTGG[C/G]TCATGCCTGTAATCC | 115677 |
rs551354152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864506 | GGTCAGGCTGGTCTC[A/G]AAACTCCTGACCTTG | 115677 |
rs551403402 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846354 | TGTACAAATTGAATA[C/T]AAAAATTCATTTTAG | 115677 |
rs551422082 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845336 | TTAGGAGATGGGAGA[C/G]ACATTTCTGCTCCCA | 115677 |
rs551484738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830557 | AGAGTGGTTGAATAA[C/T]GGCTGATCTGCTGGG | 115677 |
rs551506207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844763 | TTGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 115677 |
rs551557124 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811538 | TCTTCCTGTTCATTG[-/T]TTTTTTTGTTATTGT | 115677 |
rs551586288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803912 | TAAACTGTTAAATCC[A/T]CTCCTGTCTCAACAC | 115677 |
rs551595595 | in-del | -/TG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795459 | ATAGGATGACTTGAC[-/TG]TTAATTAGTTGTCCA | 115677 |
rs551601383 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840980 | AGAATCGGCTGGGTG[C/T]GATGGCCCACACTCA | 115677 |
rs551638556 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865450 | GACAGGCAATCAAGA[C/T]ACCAATGAGATCAAC | 115677 |
rs551712271 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843168 | GGAGCTTTGTGTGAC[A/C]TTGAAGATGGAGGTC | 115677 |
rs551739824 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785925 | CCAGCTAATTTTTTT[G/T]TATTTTTAGTAGAGA | 115677 |
rs551740690 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790080 | GTAAAATTTGCTAAT[A/G]TTCTACTTTAAGTGC | 115677 |
rs551801224 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851472 | GAGGGACTTACATTG[-/A]AAAAATTGAAAGCAA | 115677 |
rs551820315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833000 | TACAATGAATCAAAA[A/G]CCAGAAATAATGCTG | 115677 |
rs551849083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791226 | CAATTCCCACCTGTG[A/T]GTGAGAACATGCGGT | 115677 |
rs551862210 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824465 | CACCACGCCTGGCTA[A/C]TTTTTGTATTTTTAG | 115677 |
rs551917959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805991 | TGTGTAAAGTAAAAG[A/G]AGGAAAGGATGGAGT | 115677 |
rs551939151 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788013 | GGGGGATGAGAAGAA[A/G]AAGATAAATCAGCAA | 115677 |
rs551946878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860067 | AATGCTTGTAGCTAT[G/T]TTTATTACTGATCAG | 115677 |
rs551997324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860555 | GGGCACCTGTAATCC[C/G]AGCTACGGGGGAGGC | 115677 |
rs551998643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793404 | TTGAGCCCAGGAGCT[C/T]TGAAACCAGCCTGGG | 115677 |
rs552076658 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809887 | TTTCCTTCATGAGAG[A/G]GGCTACAAATTGGAA | 115677 |
rs552105887 | snp | A/G | 1.69347e-05 | 0.00290982 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834311 | CAATCTATGACTGAG[A/G]AGGAGAAGCGGAAGG | 115677 |
rs552137670 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854281 | AAATCCTCACACTTC[G/T]TGTTTGTGAAGCTCC | 115677 |
rs552161322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821462 | TTTGTGACATACATA[A/C]TGAGTGCCTGTTATG | 115677 |
rs552191371 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795323 | TTAATGGAAGTAATG[A/G/T]CACATAAATATTAAC | 115677 |
rs552212739 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849764 | GCACATACCCAGCAG[C/T]CTTACACTGCCCCCA | 115677 |
rs552249170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820788 | ACCACCAAAGCCCAA[C/T]TTTTTTTTCCTCAAG | 115677 |
rs552424642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826848 | CATAGACATTTTCAT[C/T]ATGCCAAAAGATTTA | 115677 |
rs552436780 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794565 | ACTGTGTTAGCCAGG[A/G]TGGTCTTGATCTCCT | 115677 |
rs552445993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816271 | GTGCCTGTCTTTAAC[A/G]CGCCTTTCACTCTGT | 115677 |
rs552457572 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839529 | ATGAATGCGATGTTT[G/T]TTCCAAGAGCAAAAA | 115677 |
rs552525305 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800818 | TCCGGACAAGTTTAT[A/C]TAAAATCTCTGAGGG | 115677 |
rs552548913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838890 | CCTCCCAAGTTCAAC[A/G]ATTCTGCCTTAGCCT | 115677 |
rs552578825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836039 | CAAAGGAAGAGAAAA[C/T]TGTCATCACCAGTAG | 115677 |
rs552588591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807734 | CTGGGAGCGAGGTAC[A/G]AGGCAAAGCCATGGG | 115677 |
rs552601152 | snp | C/G | 0.000100455 | 0.00708644 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855443 | GAGACATTGAAAAAG[C/G]CTCAAAAGACAAGGA | 115677 |
rs552601841 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862066 | TAAGAATCATTCTCA[A/G]ATATTTTAATTGCCT | 115677 |
rs552700032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835043 | GCCTTAACTATAGTA[A/C]ATTTAAATGCATATT | 115677 |
rs552701449 | in-del | -/ATAT | 0.024491 | 0.107915 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841297 | GAATGCTTTAAATAT[-/ATAT]ATATATATAAAGTTG | 115677 |
rs552705569 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801415 | TATAGAGATAGGAAT[C/T]TCCTGCTATATTGCC | 115677 |
rs552720030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848743 | AGAGTAGTTAAATTT[C/G]TAGAGACAGAAAGTA | 115677 |
rs552814210 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808741 | CTTACTATGTCCTTG[G/T]ATAGAAAGTCTAAAC | 115677 |
rs552852714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862964 | CTATTTATTGGGTGT[C/T]TCCTTTGCAGCATTT | 115677 |
rs552911828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862877 | ATTATCCACGACAAG[A/G]ACATGGCTCCCAGAG | 115677 |
rs552914915 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835685 | CAGATGCTGGAAGGG[-/A]AAACACAGTGAGGGC | 115677 |
rs552923317 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857024 | AGTATTCTCCAAACA[A/G]AGTCGTTCTTTAAGG | 115677 |
rs552946073 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836502 | ACACCCAAGCGGGGG[G/T]CATTCATTTTCTCAT | 115677 |
rs552955166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821864 | ATCGGAGAGGCTGCC[A/G]GAGTCAGATCATGCA | 115677 |
rs552970297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807953 | GCAGCCCCTTACTTT[A/T]AGAGGTTGAATGTGA | 115677 |
rs552985986 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805775 | TCTTGGTGGCTTAGC[C/T]TGGATATCAGACAAT | 115677 |
rs552996984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855854 | ACTTTTGAAACAATG[C/T]AAAAACCTTTCAAAT | 115677 |
rs553128837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848985 | ATAAAGAAATTTAAA[A/T]TAATTTTAATCACCA | 115677 |
rs553149159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812141 | AGTACTAGGTATGAT[C/T]ATGTGTAAAGCTTTT | 115677 |
rs553190733 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784752 | TTCCCTCTTTTTGGC[A/G]TCATATTGTATAGTC | 115677 |
rs553201256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850166 | GATCCTCCCACCCTG[G/T]CCTCCCAACGTGCTG | 115677 |
rs553209979 | in-del | -/GTT | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848804 | AGGAAATGAGAAGTC[-/GTT]GTTTCATGGGTACGG | 115677 |
rs553283427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816378 | AAGGGCCTTCGAGAG[C/T]TGAACTCTGCCTTCC | 115677 |
rs553289233 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803208 | TTTGTTCCATGTTTG[C/T]TCGTTTTGGTAATGT | 115677 |
rs553360912 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850594 | CTCTGGAATTCTTCC[C/T]AATTTTTTTTTTTTT | 115677 |
rs553366399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811892 | CAAGTCTCTTCTGAT[G/T]CCTCAGACTGGGTTT | 115677 |
rs553425393 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794930 | GTATTGCAGGCACAG[A/C]ATATAAAATTTCAAA | 115677 |
rs553427972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818308 | GCAGGTGTGTGCCAC[G/T]GCTCTGGGCTAATTT | 115677 |
rs553428020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811200 | AGTTTATATGTGCAG[A/G]AGGGGCATAAAATAG | 115677 |
rs553440973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803978 | CAGGACAGGGATGGG[A/G]TAAGTGGCAGCAAAA | 115677 |
rs553477223 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835959 | ACCTTTGAAATAGTC[G/T]ATATCTTCTACAAAA | 115677 |
rs553477268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842743 | AAATCACTTCCTATT[C/T]AAGGGTCTCAATCTC | 115677 |
rs553514018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841649 | GCCAGGTGTTGGGCA[A/G]TGTGCCATTTGCCTT | 115677 |
rs553524554 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825801 | GGTCTCTTTTGATGA[C/T]GAAAGAGATAAGAAG | 115677 |
rs553601714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837560 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 115677 |
rs553631637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863817 | GAAACCCTCAAAGTA[C/T]GGACACCAAGAAAGA | 115677 |
rs553637696 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828654 | TTTAAAATAAATGAA[A/T]AATAAAAAACACAAA | 115677 |
rs553704972 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843758 | GAAACAAGAATTATT[C/G]TACCCCTGTAGGGGG | 115677 |
rs553741241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859261 | CATAAAATACTAATA[C/T]ATTACCAAGGTTTCC | 115677 |
rs553771012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796811 | CTGCCCAGAAGGTCA[C/G]ACTTATCTTCTGTCT | 115677 |
rs553822022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844474 | AGTACTTGGTGCTCA[A/G]TGCTCCTCTTTTAGG | 115677 |
rs553869999 | snp | C/T | 4.98948e-05 | 0.00499449 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851058 | TAACAACTGGCTGAT[C/T]TTACCCCAATTTTCA | 115677 |
rs553879662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819182 | TCCCCTTGCATGTGG[C/T]ACTTTTTCAGCTTGA | 115677 |
rs553907795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857679 | GTTTCTGCTGTGATT[A/G]GAGATCATGAGTGGA | 115677 |
rs553909814 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816447 | CCTCTCTCCTTACTG[A/G]GCCACTTGCAATCCC | 115677 |
rs553963351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797460 | GTGCAATGGATAGCA[A/G]TAGTACAAAGGCAAG | 115677 |
rs553985915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844890 | GAAAAAAAAAAAAAG[A/G]TTCAGCCTGGACCTC | 115677 |
rs554025594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798225 | TGCCTGACACGTGGT[A/G]TGTCCTTTAAATGTG | 115677 |
rs554052365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845767 | CTAAAAATATTTAAG[A/G]CCTAGTTTTAGTTTT | 115677 |
rs554112353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787600 | GGGCAAAGGCCTTAC[A/C]TTTTATAGCTGATCC | 115677 |
rs554120582 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799395 | GAACTCAGTCTCCTC[C/T]TCCCAAAGTCCCCTT | 115677 |
rs554129197 | snp | A/G/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865825 | TTCTTATATACACCA[A/G/T]TAACAGACAAACAGA | 115677 |
rs554162156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825377 | ATAATAGGCCTTGGT[A/G]ATGATATTTAACTTG | 115677 |
rs554266466 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824457 | GCGCCTGCCACCACG[A/C/T]CTGGCTAATTTTTGT | 115677 |
rs554307960 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786001 | CAAGTGATCCACCTG[C/T]CTCGGCCTCCCAAAG | 115677 |
rs554360702 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806101 | AACAAGTACATGGAA[C/T]CCCTTCAGAGAGGGG | 115677 |
rs554367667 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858725 | CCATCAATTGGATGT[C/T]TTCTGTCCATGGCTG | 115677 |
rs554422083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805563 | AAACAATCACATAGA[A/G]ATCAAGGACAAGTAA | 115677 |
rs554452390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852183 | CCCATACTCAAAGGT[A/G]GGTGTGAGGGAAGAT | 115677 |
rs554544647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812682 | CCAAAAGGCAGGAAA[A/T]TGTGGGAAGGTAAAT | 115677 |
rs554557964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807839 | TTTTGGGACAAAAGT[G/T]AGAAAGTACTGGTCT | 115677 |
rs554570194 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823934 | TACAAAATTAGCCGG[G/T]CATTGTGGTACGTGC | 115677 |
rs554576765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792841 | CAGTAATAATAGTAA[A/G]TGTTTATTAAACAGT | 115677 |
rs554594944 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800230 | TTTACATGAGTGAGG[G/T]CAGGGGACACCTGAA | 115677 |
rs554601568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839023 | CTCCTGACCACAGGT[C/G]ATCTGCCCGACTTGG | 115677 |
rs554638119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799111 | TGGAAATTCTTGGCA[A/G]ACAACTCAGGAGCTT | 115677 |
rs554638582 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862318 | TATTGGTATTCCCAT[G/T]TCATAGCAGAGGAGA | 115677 |
rs554691477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846386 | GTCCTACGAAGTGTT[C/G]TCTTATTCCTTTTTA | 115677 |
rs554701997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800259 | AAGATCCATCCAGCT[A/G]AACTACAGATTTGTG | 115677 |
rs554711834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815127 | GCCAGAGAATGTTTC[C/T]TTTCCAAACTCAGCT | 115677 |
rs554741163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815851 | AAAACAGGGTTTATC[C/T]ACTCTTCTCCAAAGC | 115677 |
rs554743682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838572 | ATCTTTGCTTTTGTC[C/T]ATCTCCACTGCTGAC | 115677 |
rs554750515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820863 | GTGTCCTTTTTAGGT[C/T]TGCTTAGCCTCAGAG | 115677 |
rs554756195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835768 | AGAATCCACAACTGT[A/C]CATGTGTGAGCACCA | 115677 |
rs554793242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835212 | CCCAAGTAGCTGGGA[C/T]TACAGGTGTGCACCA | 115677 |
rs554794551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861590 | TCCATACACAGCTAG[C/G]GATGATGATAACATG | 115677 |
rs554831195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789304 | GACTGGGTAATGTAT[A/G]AAGGAAAGAGGTTTA | 115677 |
rs554831929 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851504 | TATCATGTTTTATCA[A/G]TGAAAATGATTTCTC | 115677 |
rs554846391 | in-del | -/A | 0.0991586 | 0.199366 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801386 | CACCACATCCTAATT[-/A]AAAAAAAAAAAATTA | 115677 |
rs554848369 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822573 | CAGACTGAAAAATGC[A/G]ATGAAAACTCTTAGG | 115677 |
rs554892100 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794749 | GTGTAAAATGGCTTA[A/G]AAAAATTAACATATA | 115677 |
rs554930515 | snp | A/G/T | 3.59028e-05 | 0.00423676 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834350 | CATGGCTGGCTGGGC[A/G/T]CATGTGCCATAGAGA | 115677 |
rs554934076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856436 | GAAAATTAGCCGGAC[A/G]TGGTGGCATACACCT | 115677 |
rs555069936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823017 | GTATTACTTTTGTTT[C/T]TGTTTTTGTTTTTGT | 115677 |
rs555071505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828881 | AAAAAGTCTAATTTA[C/T]ACAATCTCAACTTTA | 115677 |
rs555101923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854673 | TCCTCCCCCAGCCCT[C/T]TGCTCCCGCCATTTT | 115677 |
rs555163352 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828829 | TTAATCACATGGGGA[-/T]TTTTTTTCACAGTAT | 115677 |
rs555172940 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788722 | ACTGCTGGAAAAGGG[A/T]GGTGTAAATATGGAG | 115677 |
rs555234243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794182 | TTCATAAGACATCCC[A/G]GAATGAATGAGTGAA | 115677 |
rs555361451 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808993 | ATAATGTGTATTATT[A/G]TTTTCTGTATCATTA | 115677 |
rs555364819 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816501 | CTCCTGCATCACCAC[A/C]ACCACCACCACACGT | 115677 |
rs555465959 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829107 | CGCTTATTAGCTTGG[C/T]ATTATGTAAAGGTAA | 115677 |
rs555511539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795909 | TTCTAAGTTGGATAG[G/T]TTTTTTTCTTCCATC | 115677 |
rs555517990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842806 | AGGCCCTTGGGTTTC[C/T]TTTAGGTTTGGCCAT | 115677 |
rs555525230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790304 | AATATATAATAAACT[A/G]AAAATGTGATGAGGA | 115677 |
rs555528154 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837732 | AGTGTTCTTGCCATC[G/T]AAAACAATGTCTTCT | 115677 |
rs555533589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837242 | ATTCCTCTCCAGATA[C/T]TGTCATGTCTCCTTT | 115677 |
rs555573613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803010 | TCATGTGTGGTGTGG[A/T]TACAAAAACACACAG | 115677 |
rs555635004 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802538 | TTGACAAGGACTGAC[A/G]TACTCTAGGCCCTTT | 115677 |
rs555641911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811977 | CTTTTCACACCGACA[A/G]CAATTATTTACATTT | 115677 |
rs555643725 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785395 | TCTCAGCTGAGGGTA[C/T]TAGATGGTACATAGA | 115677 |
rs555653413 | snp | A/G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818066 | ACAGAAGAATTTGAG[A/G/T]TTATTAAAATTCCTT | 115677 |
rs555704971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818408 | TGATTCTCCTACCTC[A/G]GCCTCTGGAGTAGAT | 115677 |
rs555713593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797547 | CAGCTGGGCCAACAT[A/G]AAGCTATAAGGACTT | 115677 |
rs555720707 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856334 | ATAATCCTAACACTT[C/T]GGGAAGCCAAGGCGG | 115677 |
rs555776979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797025 | TCACTGAGTACTGTG[A/G]GAGGCAGACCATTGA | 115677 |
rs555830889 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832080 | TGGCCCAGTGAGGGG[G/T]GGGTAGTGATATGTA | 115677 |
rs555840084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804076 | GGAAATGGTGGGCAG[C/T]TTTAATTAAGTTTAA | 115677 |
rs555865422 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806079 | TCCAAATACTACGCA[A/G]ATGGTGAACAAGTAC | 115677 |
rs555872640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836606 | TCAGCAGTCTTGATT[A/C]CCACCAGAAGCTGAT | 115677 |
rs555875838 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844269 | CACGCAGCTTATGCA[C/T]GGCCCCTGGTGAAGC | 115677 |
rs555889991 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841542 | GAGAGGAAACCATCT[C/T]ATCAAGCTGTCCATA | 115677 |
rs555958549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824999 | CCTGGGCTCAAGTAA[G/T]CCTCCTGCCTTGGCC | 115677 |
rs555985968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858331 | ACATGATTTCATTAC[A/G]CATGCTCTGCATCTG | 115677 |
rs555995726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832561 | GCAAACTTGGTGTTA[C/T]TTCCAAAGCTTCTGC | 115677 |
rs556048859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864304 | TTTTTTTTCTGAGAC[A/G]GAGTCTTGCCCTGTT | 115677 |
rs556119533 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788714 | AGTTTCTCACTGCTG[A/G]AAAAGGGAGGTGTAA | 115677 |
rs556122087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817585 | TCCCTCACCACAATA[C/T]TCCCTGTCCTCCCCT | 115677 |
rs556122748 | snp | A/T | 4.97863e-05 | 0.00498906 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831501 | TGAAAAGACAGCAAA[A/T]CTTGTCATTAGCAAC | 115677 |
rs556124782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823815 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 115677 |
rs556136004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853184 | GTTGTCTAAGAGAAA[C/G]GACTGTGTCTCAAAA | 115677 |
rs556192636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791407 | TTGTTGGACATTTGG[C/G]TTGGTTCCAAGTCTT | 115677 |
rs556220571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812506 | ACAAAAGAAAAACAA[A/G]CAGAAACTTATTAAT | 115677 |
rs556225553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838000 | CTCTATTCTCTTCAC[C/T]ATTGTCTCTCCAGTG | 115677 |
rs556259104 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852042 | TGTCTCAGCCTACTC[A/C]CCGCAAAATGAGTGA | 115677 |
rs556267047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825571 | ATATTAAATGAGATC[A/G]TGTGTGTGGAGAGCT | 115677 |
rs556301402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864708 | TTTGGCTTCATCTGA[A/G]TCAAGTGCAGAAAAT | 115677 |
rs556305132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813391 | GCTAAACAGACTCAA[C/T]AGTGAACTGAAAAAC | 115677 |
rs556306972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786689 | CCAGCCACTTGATCC[C/T]TCAAGTGGCCAGCTT | 115677 |
rs556317741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847273 | ATCAATATGTTAATA[G/T]CAGTCACTTCTGGGT | 115677 |
rs556374618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819803 | TACAATCGTGCTGTT[C/G]AGAGAGGCAACATCC | 115677 |
rs556449411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792947 | TAAGAAATTTCTCCC[A/G]AAGTTAGCATACTAA | 115677 |
rs556450185 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853867 | GTAATAAATAATATA[A/C]AGAAATATTTATTTA | 115677 |
rs556519474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860702 | AACAAACAGAAAAAA[C/G]AACTTGAGGAAAACA | 115677 |
rs556565039 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806370 | CAAGCAGAAAGAGCA[A/G]GTGGGCCAAGCTTGA | 115677 |
rs556632409 | in-del | -/GAAA | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792315 | AAGGAAAAATTTAGT[-/GAAA]GAAAAAAATGCATTA | 115677 |
rs556641765 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844672 | TCAGGAGATCGAGAC[A/C]ATCCTGGCTAACACG | 115677 |
rs556769178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800065 | CTCTTCCACTCACTC[C/T]TGTGGCTCCTCTGCC | 115677 |
rs556775882 | in-del | -/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863918 | CGTGATCTTTTTTTA[-/T]TTTTTTTTTTGAGGC | 115677 |
rs556792095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787678 | GTAGAATGAATATGC[A/T]TTTACAGAAAGAGGA | 115677 |
rs556824774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833966 | AATTCAAAATCCTCT[G/T]GAGGGTACCCGATAT | 115677 |
rs556828422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799230 | GGTTGCAGCCCTCAA[G/T]CTTGGCCCAAGTAAA | 115677 |
rs556907033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794890 | GTGCCACTGCACCTG[A/G]CTCTTAGTAAATACT | 115677 |
rs556957681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815253 | CTTAGCTTCTTTTAT[C/G]CAATTAGCTACCTCA | 115677 |
rs556960888 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788115 | CTTGGTGGTTTATAC[A/C]TGTAATTCAAGCACA | 115677 |
rs556968249 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801550 | CTTTGAATGGAGCCT[A/G]CACACCAGGGGCAGG | 115677 |
rs556968643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794359 | AAAGGGATGATTTTT[C/T]TTTTTTTTTTGAGAT | 115677 |
rs556971149 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834479 | AAGGGGATTCCAAAT[A/C]ATTACTGGCGTGCGC | 115677 |
rs556998426 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861674 | TTTCCAAAACATGCA[A/T]GCAATTACTATTATT | 115677 |
rs557031818 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800945 | AGATGGGGTGTTGCT[A/C]TGTTGACCAGGCTGG | 115677 |
rs557076094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807899 | TCTAGACCTGGTAGC[C/T]CATGGGTCAATGGAA | 115677 |
rs557119081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855674 | AATCACATTTTGGTC[C/T]ATTTATGAAACCTAT | 115677 |
rs557139585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816060 | CTCTTAAACTATTCT[G/T]CCTAGAAGTGCTGCC | 115677 |
rs557152307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822517 | CTGCCCAAATGAAAT[A/G]ACATAATAAATAATT | 115677 |
rs557169473 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838221 | CCAAAGATAATCTTT[A/C]TTCCTGTGTTCTCTG | 115677 |
rs557171716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808772 | ACCATTAAAAAGTCA[A/G]TTTTCCCAAATTGAT | 115677 |
rs557184327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856340 | CTAACACTTTGGGAA[A/G]CCAAGGCGGGTGGAT | 115677 |
rs557208315 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862367 | AGGTGCTTTGGCTAA[C/T]GTCACAGGCTGTGGC | 115677 |
rs557271784 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825323 | TGAGTTGCATAGCTG[A/G]ATTCTTCCTCAGTGT | 115677 |
rs557285758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821796 | GAGGCAGGATGGCAG[G/T]TGGCCACTGAATAGG | 115677 |
rs557321428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789794 | AGTAGCTGGTACAAA[C/T]TGAAAGTCAGACCGA | 115677 |
rs557330442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850317 | AAACTTCTGTCATCT[C/T]ACACAAAATAAAGAG | 115677 |
rs557350804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817704 | GGCCAGAGTGAGCCG[A/G]GGCTCAGTGAGACTC | 115677 |
rs557427195 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811140 | CAAGAAAGGCTCACT[C/T]TAATGGCTCATGGTT | 115677 |
rs557461762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823173 | AGGCGTGAGCCACCA[C/T]ACCTGGCTAATTTTT | 115677 |
rs557468012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857498 | GGAGGTGGGCCTCCT[A/G]GCCTTTGTGCTGAGT | 115677 |
rs557501983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848179 | GCAGAATTTGTTTTA[C/T]GTATTTGTTATGAGG | 115677 |
rs557588939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829144 | GTACAATCCTCAAAT[A/G]TCCTAAAAATTACAG | 115677 |
rs557765505 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858819 | ATAATGGTGAGGAGG[C/G]GGCTGGATAAGCAAG | 115677 |
rs557860944 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806526 | GAAACATTTTCCTAA[C/T]GGCCGAATGGGAAAT | 115677 |
rs557915876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837279 | TACATCTTTTTTTTT[A/T]ATAATACACTTTTTT | 115677 |
rs557926688 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816166 | CTCTTACCCCTTAAG[C/G]CTTTTACTCTGACAG | 115677 |
rs557931096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831633 | CTAGCATTAGTACTT[C/T]TAAGTGCTAACTGAA | 115677 |
rs557955312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796729 | TTCGTTTCCTGCTTG[G/T]CAAGGCCATTTTAAT | 115677 |
rs557957296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790362 | TACGTCACCACAAAA[C/T]ATTTACTAACTTCAA | 115677 |
rs558017298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796269 | CGGGAGTTGGCCTTC[A/G]GAAGACATGTTAAGG | 115677 |
rs558022400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804724 | GCCCACACCAATGTA[C/G]CCATGTATGGAACTC | 115677 |
rs558045035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789101 | TAGCTGAACCAAGAG[G/T]TGGGCAGGGAAAGCA | 115677 |
rs558052697 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785861 | GTTCAAGTGATTCTC[A/G]TGCCTCAGCCTCCTG | 115677 |
rs558062943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852118 | TAAGCTAATCTCAGA[A/C]GTGACATCTCATCAT | 115677 |
rs558095394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792065 | TCCTTGCCCATGCCT[A/G]TGTCCTGAATGGTAT | 115677 |
rs558101957 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859178 | CCACCAAAAATCTAC[A/C]TTCTACAATCAACAC | 115677 |
rs558125775 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822113 | CAGCACTCTTTTTCT[C/T]TCCTCTCCATCAACT | 115677 |
rs558162895 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819249 | AAATCATTCTAAGTG[G/T]GGTGTGCCTTGCTGC | 115677 |
rs558204905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824412 | CAAGCGATTCTCGCA[C/T]CTCAGCCTCCCAAGT | 115677 |
rs558221785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797656 | TTTAAAATTAAAGTT[A/G]GCATAAGTGTTAACC | 115677 |
rs558241461 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784983 | AGTCATTCAATACAT[G/T]GCAGACTGAAGAATG | 115677 |
rs558243407 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808601 | TCAATAAGACAATAC[A/G]TAAAAATCCATAGCT | 115677 |
rs558278069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830905 | CATGATTGCACATGT[G/T]TACATGCTTTTTACA | 115677 |
rs558352601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819860 | TCGGTGACATTTGCT[G/T]TCAGAGTCCCCATCC | 115677 |
rs558381219 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795941 | TGAGGCTGTGGGCAA[A/G]GGCCGAAACCCTTAA | 115677 |
rs558411361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812050 | TATGCTGACCTCTTA[C/G]AGCCTGGCCTTTTGA | 115677 |
rs558513266 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792259 | GATGCCATCTATGAC[C/T]TTCAAGAGTCATAAA | 115677 |
rs558515138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805477 | CATGTGCAAGAAAGG[C/T]GAAGTAAGATCCAAT | 115677 |
rs558531406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818480 | TTTTAATTAATTCCT[C/T]ATAGACACAGGGGGC | 115677 |
rs558552778 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833360 | GCAGAGGCTTCCCAC[A/G]TTTAGAGGGAGGCAG | 115677 |
rs558583495 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835672 | TGGCCACATGTCCCA[C/G]ATGCTGGAAGGGAAA | 115677 |
rs558627076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852653 | GAAGTACAGCCAAAG[C/T]TGACCTCCCTGGACC | 115677 |
rs558635785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799421 | CCCTTGGGCCATTTT[G/T]GGGGACTGGAGGAAT | 115677 |
rs558658999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838193 | CCAAAATCCAACCAT[A/C]ACTTTTTTTCTACCA | 115677 |
rs558713378 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840503 | CCACTGCACTCCAGC[C/T]TGGGGGACAGGGCGA | 115677 |
rs558737136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826450 | CTTTCTTTCTCTTCC[C/G]TCCCTTCCTCCCTTG | 115677 |
rs558844444 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844535 | TTGTATTAATCATGA[C/T]ATTATGAGAACATTG | 115677 |
rs558865719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807217 | TCAAGTGATTTCACC[C/T]CCACAAAGCAGGTAA | 115677 |
rs558872737 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834489 | CAAATCATTACTGGC[A/G]TGCGCGCGCGCGCGC | 115677 |
rs558954780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861755 | TTTTTGGTTATATAA[C/T]ATATGCAGTCCATAC | 115677 |
rs558957665 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829597 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCACTGC | 115677 |
rs559076472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788401 | GAATCACTGTGGCCC[A/G]GAGTGGAATGATGGG | 115677 |
rs559113299 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832523 | GATGCCAAATAACTA[A/G]AGACAGACGCACTCA | 115677 |
rs559115917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854296 | TTGTTTGTGAAGCTC[C/T]ATCTAAAGGTAATCT | 115677 |
rs559152023 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830172 | AAAATATTTTTCACA[-/C]TGCATAATAATATGA | 115677 |
rs559160011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788174 | GAGCCCAGGAGTTCA[A/G]GGCTGCAGTGAGCTA | 115677 |
rs559161971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794170 | CAAAGATGGTGCTTC[A/C]TAAGACATCCCGGAA | 115677 |
rs559194904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800189 | CAGATGCATGGCTCT[A/G]CCAAGCCCTGTGTAG | 115677 |
rs559211151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847381 | CTTAAAAGTCAGATT[C/G]CTGATCACCTCCCTA | 115677 |
rs559224561 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807122 | GGTGGCTTGCAAACT[A/G]TGCTCCATGGAACCC | 115677 |
rs559224921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793695 | CCCTTTTGTGACTCT[A/G]TTTACCTTTTGGTTA | 115677 |
rs559329375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797924 | CATCCCGCAGTATCC[A/G]TGGGGCATTGGTTTC | 115677 |
rs559438565 | in-del | -/AATT | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865468 | AATGAGATCAACCCA[-/AATT]AATTAGGGGATGGTA | 115677 |
rs559474314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829312 | TCTCTTTCTTTTTTT[C/T]TCTCTCTCTCCCTTT | 115677 |
rs559511019 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788242 | TAAGATCCTACCTCA[-/A]AAAAAAAAAAAAAAA | 115677 |
rs559538487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820507 | CTGTCTGGACAGTCT[C/G]TTTAGGTGCAATATA | 115677 |
rs559582020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816765 | TCTCTTTCCCTAGAG[A/G]CTGAACTCCTTGAGG | 115677 |
rs559595387 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796644 | TTACCTCATCTGTTT[A/G]TATCTTTTAACCAAC | 115677 |
rs559603015 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847638 | ATGCTTGGGCCCCAG[A/G]CAGGCTCTAAATCTG | 115677 |
rs559710326 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822073 | GTTCATCAAGGGTGA[A/T]GGTCTCTCCCAGCTG | 115677 |
rs559736582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862892 | GACATGGCTCCCAGA[A/G]CCAATGGAAAATCAA | 115677 |
rs559758482 | in-del | -/TATA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841303 | CTTTAAATATATATA[-/TATA]AAGTTGGAGAATAAT | 115677 |
rs559816633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842242 | GGGAGTGAGAGACAG[G/T]AGGGCAGAAGAAGGT | 115677 |
rs559834496 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846726 | TTATTTTTAAAAGCC[A/G]TCTGCAATATGTGTC | 115677 |
rs559891737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849372 | CTTCTTTTCTTTTTT[C/T]TGAGATGGAATCTCA | 115677 |
rs559907390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795968 | TTAAAAAATTTTTTT[A/T]AAAATATGTGCATTA | 115677 |
rs559926019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835368 | ATAGGCATGAGCCAC[C/T]GCCCCTGGCCAGCCT | 115677 |
rs559926752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856569 | GACAGAGCAAGACTC[C/T]GTCTTAAAAAAAAAA | 115677 |
rs559956305 | snp | A/G | 1.6607e-05 | 0.00288153 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843015 | TAAACTGACAAAATC[A/G]ACTGAAAAGTTGGAA | 115677 |
rs559966128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831031 | TTCCCATGAATTGTA[A/G]TAGTGATTGATAAGC | 115677 |
rs559970545 | snp | A/G | 7.78528e-05 | 0.00623862 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802673 | ACTGACAGATTGTCC[A/G]GTGAGTAGCTCAGTG | 115677 |
rs559979531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857015 | GTCTAAAATAGTATT[C/T]TCCAAACAGAGTCGT | 115677 |
rs560104284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823981 | TTGAGAGGCTAAGGC[A/T]AAAGAATCACTTGAA | 115677 |
rs560105733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863258 | TGTTAATAGATTATG[A/T]CAATTTACTGACGAG | 115677 |
rs560139949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858521 | AATTGTTGAGAAAAC[C/T]GGAGGCACTTAGATT | 115677 |
rs560183362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813599 | TGAAACCCTCCATTC[A/G]CTTATTCTAGAGTGA | 115677 |
rs560194277 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787111 | AACAGCTGCTTCTGG[C/G]ATCAGGTAAGAAAAG | 115677 |
rs560215879 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810321 | GGGTAAATGGATATG[G/T]TAAGACTGTTCCTGT | 115677 |
rs560221797 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838484 | ACATCAAGTGATCCG[C/G]CCGCCTTGGCCTCCC | 115677 |
rs560226936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857848 | TTGGCAATTTCAATA[A/G]TTCTTTGGTGAAAGA | 115677 |
rs560253695 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789764 | TAGTAACCTTGGGAA[A/G]CTGAAACTGCTTAAA | 115677 |
rs560268312 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785812 | GGAGTGCAGTGGCAC[A/G]GGATCTCAGCTCACT | 115677 |
rs560294743 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852070 | TGATCAAGACAGACA[A/C/G]AGCCAGAGTGCCCAA | 115677 |
rs560346882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823347 | AGGGCTGTCATAACA[A/C]AGTACCACAGAATGA | 115677 |
rs560438450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830320 | CTTCTTTTCTGCATT[G/T]CCCCTCTCCACTGCA | 115677 |
rs560463883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790442 | AATCAGGTGAACACC[A/T]TCAGTAATGGGGCAA | 115677 |
rs560496825 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812120 | CATTTTCAGCATCGT[C/G]TTCTTAGTACTAGGT | 115677 |
rs560556758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791119 | TTAACATTAGGTATA[G/T]CTCCTAATGCTATCC | 115677 |
rs560622599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818570 | TCTAATATTGATTAC[A/G]TGGTCACATATTCTT | 115677 |
rs560642479 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786428 | TCAAGCATGCGCACT[A/G]TGAGGCAAAATGGGG | 115677 |
rs560646011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838287 | TTCTAACTCAAACCA[A/G]ATCCTTCAGTGGCAC | 115677 |
rs560646083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832317 | AACAGATGGGATCCA[C/T]ATGCACAGAAGATTA | 115677 |
rs560690042 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791756 | AGTGACGGTTTTTTT[A/C]ATGTGTTTTTTGGCT | 115677 |
rs560711960 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806578 | TCTATTTGAGAAGGG[G/T]TTATTATTTTTTTAG | 115677 |
rs560732036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819377 | GCCGTGGAAGTGTGC[A/G]CGGAAAAGCATGGAA | 115677 |
rs560735594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837714 | CCCCATCTTTCCACT[A/G]AGAGTGTTCTTGCCA | 115677 |
rs560775721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825132 | CATGGCAAGTACATA[A/C]CATCAAGCATGGCTT | 115677 |
rs560780628 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836632 | CTGATCTAAACCTCC[A/G]TTCTCCTCACACCTC | 115677 |
rs560809875 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789984 | AATGCCGCTGGTTTT[C/T]AGTCAGGCCACAGTG | 115677 |
rs560835082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813679 | CCTCATAGCTTTACA[A/T]CCTTATAGAGAAGAA | 115677 |
rs560872304 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848172 | CAACTGAGCAGAATT[C/T]GTTTTACGTATTTGT | 115677 |
rs560880522 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798647 | ACAGTAAATCTAACC[A/G]GAAGCCAGGCTGGAA | 115677 |
rs561025331 | in-del | -/TAAT | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864449 | GCCACCACACCCAGC[-/TAAT]TAATTTTTGTATTTT | 115677 |
rs561051364 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854024 | AGGTGCACACCACCA[A/C]GCCCGGCTAATTTTT | 115677 |
rs561093014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853396 | TTTGTAAGGTTACCA[A/T]AAATGCCATGTTCAA | 115677 |
rs561093015 | snp | C/T | 3.3222e-05 | 0.00407553 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860939 | ACAATCATTTTGGCC[C/T]GGGTCCTACTGGCAG | 115677 |
rs561139115 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792144 | AGTCTTTAATCCATC[C/T]TGAATTAATTTTTGT | 115677 |
rs561142564 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852458 | GCTCCCCTCTTGATA[G/T]TCTTAATTGTAGTGT | 115677 |
rs561179201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860446 | GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCA | 115677 |
rs561200621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827388 | ACCCAGCAGGGAACA[A/G]GAACTGGACTCCAAC | 115677 |
rs561230902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838760 | CCTTCAAAGGCTTCC[A/C]AATGACTTCAGAATA | 115677 |
rs561235807 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819253 | CATTCTAAGTGGGGT[A/G]TGCCTTGCTGCCTCT | 115677 |
rs561238454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787846 | GTGATTTTCATTTTT[G/T]TTAATTTTTTTCAGA | 115677 |
rs561238818 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842296 | GGCTGCTTCTGAGGC[C/T]TTGATTTTGTGGTAT | 115677 |
rs561288877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826757 | TACATGCAATAATAA[A/G]CACCCATTTTAAGCA | 115677 |
rs561288991 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834497 | TACTGGCGTGCGCGC[A/G]CGCGCGCGCGCACAC | 115677 |
rs561369274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793235 | TTCCTGGCAACAGCC[A/T]CCCCACTCTTCCTAA | 115677 |
rs561430670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799569 | TGCCTCCTCACAACC[C/T]ATATCCAGGAGAGGT | 115677 |
rs561434671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168846835 | TGCTTTCTCAGTTCT[C/T]CCAAGGATGGCACTT | 115677 |
rs561461554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854983 | AACACATACATGATA[C/T]TACATTTGGGCCATT | 115677 |
rs561536587 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809426 | GGCTGAGAAATGACC[G/T]TATTTCAGGAGTATG | 115677 |
rs561547091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821247 | ACTCAGAAGGGTTTA[C/T]GTGTCTAGGTATTTC | 115677 |
rs561580911 | in-del | -/AG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807281 | CATACACACACACAC[-/AG]AGAGAGAGAGAGAAC | 115677 |
rs561612613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816181 | CCTTTTACTCTGACA[A/G]AGCTGTGCCCCTTTA | 115677 |
rs561643016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862696 | CATGGAAAGGTATTA[C/T]GTAGTGGCTTTATAA | 115677 |
rs561658244 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821933 | ACCCCTAGTAGACTT[C/G]GGCTCTCAACACATT | 115677 |
rs561687364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857359 | AGGGGAAAGGAAAGA[C/T]GTGGTTGCAGAGGGA | 115677 |
rs561711590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836041 | AAGGAAGAGAAAATT[A/G]TCATCACCAGTAGCT | 115677 |
rs561843124 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833099 | AAATAAAAGATTTCA[-/T]TTTTTTTAAATAAAG | 115677 |
rs561868161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815600 | TCAATCCATGATTCA[C/T]TGCGGACACTGTCAA | 115677 |
rs561950845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788975 | CCTCAGAGCCTAGAG[G/T]CAATGCCTCCTCAGT | 115677 |
rs561962661 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802008 | ATAGTTCTATAGGTG[C/T]AGGTTCCTAGTTGTT | 115677 |
rs561965379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802738 | GTGGATTTGTATATT[A/G]ATGGATTTTAACTTA | 115677 |
rs562015460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794602 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 115677 |
rs562042657 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803974 | AGGCCAGGACAGGGA[C/T]GGGGTAAGTGGCAGC | 115677 |
rs562124778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831176 | AAGGCACCCACACAT[C/T]AGCTGTGTGATGAGG | 115677 |
rs562243552 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796367 | GCTGACAGCTAGCTG[A/C]TCCCACCTGACCCCT | 115677 |
rs562302997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850638 | CAAGGCCTGGCTAGG[C/T]GCGGTGGCTCATGCC | 115677 |
rs562304863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857717 | TAATCTGAGAATCAT[G/T]TAAGGAGATAAATTT | 115677 |
rs562327893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811330 | GCATTTGGCCAAGGG[A/G]AGAAATAGATCAGCT | 115677 |
rs562361716 | in-del | -/A | 0.000814001 | 0.0201578 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855890 | CTGTACGTAGAAGTT[-/A]AGGCATGTCAGACTG | 115677 |
rs562375477 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790560 | TCATGAGCAAACATC[A/C]GATAAGTCCAAATTG | 115677 |
rs562389943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857143 | GCTCTGCTGTTTACA[C/G]GGACCTGGGTCAACT | 115677 |
rs562410204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837394 | GGCTTACTGCAAGCT[C/T]CGCCTTCTGGGTTCA | 115677 |
rs562440969 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848362 | AATCCATTTGACTCC[A/C]ATTGACATATGAAAA | 115677 |
rs562485028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837598 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGTCACAAT | 115677 |
rs562501942 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787379 | ACTGCTTACACTGCC[A/G]CAGAGACCTCTTTCC | 115677 |
rs562506550 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858753 | CTGTGACACCCTGGC[A/C]GGGATATTAGGGTTG | 115677 |
rs562578551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852292 | CAGATTATCGGAGGC[C/T]TATTTTGAGGGTACT | 115677 |
rs562663510 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865427 | CACAGATCAATTCCA[A/G]GAAGAGAGACAGGCA | 115677 |
rs562666206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851805 | AAACAAACATGTATT[A/G]TCTCATAGTTTATGT | 115677 |
rs562777862 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841662 | CAGTGTGCCATTTGC[C/T]TTATCTGTGTTACCT | 115677 |
rs562809550 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785659 | AGGCTTTGTGAGGAG[A/T]ATGAGGAAGTCAGGG | 115677 |
rs562827804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797865 | TCAAAATAATACATA[C/T]CTACCTCAAATGATA | 115677 |
rs562885260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812154 | ATCATGTGTAAAGCT[C/T]TTCACTGTGCTGAAA | 115677 |
rs562888673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805052 | CATTCTAAAAAATAT[A/G]TAATTCATTTCCTTT | 115677 |
rs562955212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804405 | CTGGGTTTCCAAACC[C/T]TCTAAACTCACAGAA | 115677 |
rs562983565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812763 | GAGCAGATAAGCAAG[G/T]GTTGGACTGTCTTTA | 115677 |
rs563038754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791861 | TAAATTTGTTTGAGT[C/T]CATTATAGATTCTGG | 115677 |
rs563058256 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838565 | CTTGAATATCTTTGC[G/T]TTTGTCTATCTCCAC | 115677 |
rs563062425 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840269 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 115677 |
rs563072320 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786863 | CTCCAGAGTAGCTGG[G/T]ACTACAGGCGCCCGC | 115677 |
rs563081987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833359 | TGCAGAGGCTTCCCA[C/T]GTTTAGAGGGAGGCA | 115677 |
rs563143458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813778 | AGTATAGTATGAGTA[C/T]AAAGAACAGATCTAA | 115677 |
rs563284279 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790811 | TGCTTTTGATGGTTG[C/T]ATTTTGGTTTTGTTG | 115677 |
rs563329488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819941 | CTTGCAACTGCACAG[A/G]TGCCTTTGGAACAGG | 115677 |
rs563332565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839301 | TGAGCACTTACTATG[A/C]GCCAAATTATAGCTT | 115677 |
rs563357053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807495 | TCAATCTGGATCAAG[G/T]TTTGTTGGGGGAATT | 115677 |
rs563422187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813080 | CCATGACAGAGAAAG[C/T]GGGAGGTGCCATCTG | 115677 |
rs563471218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847490 | CCTGCTCTAGAAAGA[A/G]CATATTTCTTTTATC | 115677 |
rs563514876 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848431 | GGGCGTGGCTCCAGG[C/G]TTCCAATCCAAATGT | 115677 |
rs563517075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835241 | CACCATGCTCGGCTA[A/T]TTTTTTTTTGCATTT | 115677 |
rs563625137 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829893 | CACATCCTCAGTGGC[-/A]AGTCAGAAGGATGAG | 115677 |
rs563642872 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860442 | TTGGGAGGCCAAGGC[A/G]GGCGGATCACCTGAG | 115677 |
rs563683019 | snp | C/T | 3.31356e-05 | 0.00407022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828231 | CATCAGTGAGTTCTC[C/T]CACCCTGGCCTTTCT | 115677 |
rs563690010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863182 | TCTTTAAATGAAACA[C/T]GACGTTGGAGCCTTA | 115677 |
rs563770836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849086 | GTAGGAATTTCAAGA[G/T]GTGAGCAAGGAGAAC | 115677 |
rs563858272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848620 | CCAAAAAGGAAGGGA[A/G]TTCTGGCACATGCTA | 115677 |
rs563859498 | in-del | -/AC | 0.0185938 | 0.0946107 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807269 | CACACACACATACAT[-/AC]ACACACACACACAGA | 115677 |
rs563902153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796284 | GGAAGACATGTTAAG[A/G]TGTGTCAAGACGTGT | 115677 |
rs563912435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816252 | GTGGGCCAGCTGAGG[C/T]CCTGTGCCTGTCTTT | 115677 |
rs564041935 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817242 | AGTTTTGGGCACTGC[C/T]CTGGGTGACCCAACA | 115677 |
rs564045570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842866 | TTGTCAACTATAGTC[A/G]CTGTTTATGACTCTA | 115677 |
rs564046291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856510 | AACTTGGGAGGCAGA[C/G]GTTGCAGTGAGCCGA | 115677 |
rs564088608 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802160 | TGCTCACAGGCCAGT[C/T]GTTTGCTCTCTCTAG | 115677 |
rs564110021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830269 | GCTTTAGTTAATGGA[C/T]GTCATGAGCACCCCC | 115677 |
rs564115856 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841873 | GGTTTAACAAAATAC[A/G]GACATCCATGTACAA | 115677 |
rs564184216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864380 | CAACCTCTGCCTCCC[A/G]GGTTCAAGGATTCTC | 115677 |
rs564195481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836667 | CACACACTCCTGGCA[C/T]AGTATCTTGCCTCCT | 115677 |
rs564223619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863934 | TTTTTTTTTTGAGGC[A/G]GAGTCTTGCTCTGTC | 115677 |
rs564226460 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809986 | AAAAAAAAATCATGT[G/T]TCGGATGCAAATCCT | 115677 |
rs564282090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857816 | GTGAAGGTAGGTACT[C/T]GATAATTGTACCCAG | 115677 |
rs564369585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795951 | GGCAAAGGCCGAAAC[C/T]CTTAAAAAATTTTTT | 115677 |
rs564396038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789603 | ACCGTATCAGCTGGA[A/G]TGTGCCTCCTATTGA | 115677 |
rs564416408 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836155 | GTCTTCACAGTTGGA[A/T]ATGATCATAACAAGT | 115677 |
rs564476492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817969 | CCAATGAAGTTTGGA[C/T]AGAAAATATCAGCAC | 115677 |
rs564510334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810826 | TCAATTGACATTTAG[C/T]TTCTCTGTTTGGGCA | 115677 |
rs564535924 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804099 | AAGTTTAAAAAGAGA[A/T]GAAGAAATAAATCCA | 115677 |
rs564550346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857218 | ATGGGGCTTTTGTGA[G/T]GGTGAAATATTATTT | 115677 |
rs564605051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803686 | ACAACATAGTAGCCA[A/G]TTCTGCCTAATTTTC | 115677 |
rs564646197 | snp | A/G | 0.000381892 | 0.013813 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851280 | CCTTGGCATTGCAGT[A/G]CCACACGCAGATTCA | 115677 |
rs564666831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837465 | CAGGCCCCGCCACCA[C/T]ACCCAGCTAATTTTT | 115677 |
rs564667707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811437 | AAAGGTATAAATGCC[A/T]GTAGCTGCACGATCC | 115677 |
rs564668703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844655 | GCGGGCGGATCAAGA[A/G]GTCAGGAGATCGAGA | 115677 |
rs564739361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812821 | GTGTGTCCCTTTGTT[G/T]TAACCTTTTTTAAAC | 115677 |
rs564752365 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857911 | TTTTAGATAGGCTTT[C/G]TTGAGTAAGGTGCTG | 115677 |
rs564756099 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785709 | GGGGGTCTCAATACA[A/G]TTAGGGAGGTAGGCC | 115677 |
rs564802734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819348 | CTGCCTCATTAGACC[A/G]GAAGCATGGAAGAGC | 115677 |
rs564825094 | snp | A/C | 1.65666e-05 | 0.00287802 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864868 | CGAGAAAAAAGAAGG[A/C]GGATGGTGGTTTGGA | 115677 |
rs564890736 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863904 | GATATATGATCCAAC[A/G]TGATCTTTTTTTATT | 115677 |
rs564927332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831247 | ACCTCAGATGGCAGA[A/C]GGGGCTAGGCAGCTC | 115677 |
rs564934422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838702 | TACAAGCCAAGCTGA[C/T]TTTTCTTAAACTCGA | 115677 |
rs565048502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860296 | ATAGTAATTGTGTAA[C/T]TGTGAAAATATTAAG | 115677 |
rs565195346 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845553 | CAGAAGCTCTTGCTA[C/T]GCCTCTCCTTCATCT | 115677 |
rs565197399 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865479 | ACCCAAATTAGGGGA[A/T]GGTAGGATATCTCTG | 115677 |
rs565210719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797930 | GCAGTATCCATGGGG[C/T]ATTGGTTTCAGGATA | 115677 |
rs565230469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825067 | CCCAGCAAAATCATT[C/T]TTAAAAATAGTAAAA | 115677 |
rs565412888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826034 | CCACTTAACAGGTGA[A/G]TGACCTAGGAAAATT | 115677 |
rs565457009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826760 | ATGCAATAATAAGCA[C/T]CCATTTTAAGCATAT | 115677 |
rs565566686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787007 | GTTCTGGGATTACAG[A/G]CGTGAGCCACCACAC | 115677 |
rs565615164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793454 | CTCTACAAAAAATAA[A/C]AAATAAATTAGCTGG | 115677 |
rs565664334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805519 | GAAAGAATCCAATCA[C/T]AAGAAAGTATTAATA | 115677 |
rs565669125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839004 | TGGCCAGGCTGTTCT[C/T]GAACTCCTGACCACA | 115677 |
rs565676664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792739 | CCTGCCTCGGCCTCC[G/T]AAAGTGCTGGGATTA | 115677 |
rs565732125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806036 | AATGTTCCATATCCC[A/G]TAATCTATGACAGTC | 115677 |
rs565747697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815794 | CAGTATATTGGACAT[A/C]TCCACCTGGAAGTCC | 115677 |
rs565786329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853657 | CTTCAACAGGGAAGG[A/T]CTAATGGTTTTAGTT | 115677 |
rs565835462 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828819 | TGTAGAAGAATTTAA[C/T]CACATGGGGATTTTT | 115677 |
rs565923613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841346 | CCAACTTCTTTGTTT[C/T]TCAGAAACATGAAAT | 115677 |
rs565966642 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792886 | TGCTGTGAAATATAT[A/G]GTATTACTTCCATTT | 115677 |
rs565971561 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790868 | CACACTAAAATATTA[A/G]AAGGTGAAGGAGCAT | 115677 |
rs565980050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833741 | CAGACAAATGCCCAA[C/G]TCTCAGGCTTGGCCA | 115677 |
rs565980196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839540 | GTTTGTTCCAAGAGC[A/G]AAAAAAGGGACGAAA | 115677 |
rs566015490 | snp | C/T | 3.41904e-05 | 0.00413449 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855470 | AGGAAGGTGTGTAAC[C/T]ATCTCTTTGAATGGC | 115677 |
rs566104211 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797605 | ATCCTAGAGATACAA[A/G]AATAACATGTCATCA | 115677 |
rs566143704 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801435 | GCTATATTGCCCAGG[A/C]TGCTCTCAAACTCCT | 115677 |
rs566172353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848773 | AGAATGGTGGTTGCC[A/G]GGGGATGCAGAGCGT | 115677 |
rs566193926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836278 | AAGCTATTCTTTATT[A/G]ATGTCATGCAATAAT | 115677 |
rs566203282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820822 | AATAAACTTAACAAC[A/G]TAAAGGAAAGCAGCA | 115677 |
rs566230920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835587 | CTAAGATATTTGTGC[A/C]TTTTGTGTATGTTAA | 115677 |
rs566257064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856115 | CAATTGCTAGAATGG[A/G]TCGACTGAAAGAATT | 115677 |
rs566263541 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824062 | CCTGGGCAACAAGAG[A/G]GAAACTCCATCTCAA | 115677 |
rs566280516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857254 | ATACCAGCACAATGC[C/T]CACAGGAGGAGCTCA | 115677 |
rs566285483 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794171 | AAAGATGGTGCTTCA[A/T]AAGACATCCCGGAAT | 115677 |
rs566348954 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800867 | TGGGAATTTGAGTTA[C/T]ATGTTATTAACCTCA | 115677 |
rs566369798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856809 | GTGCATTTCCTAGAT[A/G]TAGTGATGAAAAGGG | 115677 |
rs566369799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864059 | TGCAACCTCCGTCTC[C/T]TGGATTCAAGTGATT | 115677 |
rs566375685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848029 | AGGGATGCAATATGT[C/T]CTAAAACCTGGCTTT | 115677 |
rs566441017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822288 | GCCTTAGCATACATC[C/T]TGCAATGACTTTCTT | 115677 |
rs566486752 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794677 | TTTTAACAAGTACTC[A/G]GAGGGCTGTTTGACT | 115677 |
rs566490703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789714 | CACAACCAATGCCAT[A/G]GAAAATCAAATATAT | 115677 |
rs566682568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810125 | CCTCACCCTCCTCCT[C/T]ACTCATTCAGGTGCC | 115677 |
rs566746363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817092 | ACTTGATCTCTTTAA[A/T]TATCTCACAACCCAC | 115677 |
rs566775453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796234 | AGGCCAAGGACTAGG[C/T]GTCGTCCAGGACTCA | 115677 |
rs566782344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843424 | AGGCTTAAGTGTTAG[A/G]TGCTTCAAAATTAGT | 115677 |
rs566821406 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784854 | ATTTTTCAAGTTCAC[A/T]GTATCAGTCTAATTC | 115677 |
rs566930405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824210 | TTACGTAGGCATTAC[A/C]TTTTCAGCCTGATCT | 115677 |
rs566994201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811932 | TCCTGGGGCCCACTG[A/T]TGGATCTGATGCATA | 115677 |
rs567019951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810939 | TTACTGGAAATTCTC[A/G]TGTCCGCAGGATAAA | 115677 |
rs567020085 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833527 | ATCCAACTTAAACCA[A/G]ATTCTGTTTGCATAA | 115677 |
rs567021556 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805368 | TTTTGACAAGGAAAA[A/G]AATTGGCTCTGGGCC | 115677 |
rs567025905 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805853 | AGGAGAATCTGACTC[A/G]CTGCAAAAATACAGA | 115677 |
rs567044420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864598 | CCAATCCTGTCTTTA[A/G]GCAATTATTTTATGA | 115677 |
rs567109129 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831768 | AGTGCTATATATTTA[C/T]GTATTTAATCATCAC | 115677 |
rs567136077 | snp | A/G | 0.000591051 | 0.0171807 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831430 | TACAGCAACTAAACA[A/G]GAAGAAAGCAAAGCT | 115677 |
rs567175846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837494 | TTTATATTTTTTAGT[A/G]GAGATGGGATTTCAC | 115677 |
rs567184122 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807794 | CCATTTACCACACTC[C/T]ACCAGTACAAATATT | 115677 |
rs567210041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805197 | GGCAAAATAGACTGA[C/T]AGCTGGGCCTTTCAA | 115677 |
rs567275228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815032 | CCCCTTACTTAAGAG[C/T]TCCTGGAATGTGGTT | 115677 |
rs567301734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826165 | GTACCTGGCAGGGAA[C/T]GAAAGCTCTGTGAAT | 115677 |
rs567390495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833501 | ATCAGCCTACTTCCT[C/G]AACAGGCTAAATCCA | 115677 |
rs567411885 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791969 | GTTTCTTTTGCTGTG[C/T]AGAAGCTCTTGAGTT | 115677 |
rs567422309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821112 | ATGATTTTTGTGCCT[A/G]GCACTGAGCTGAACA | 115677 |
rs567425057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833083 | TATCAAGTCATTTTT[G/T]TAAATAAAAGATTTC | 115677 |
rs567428549 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793374 | CACTTTGGAAGGCTG[A/G]GGTGGGTGGATTGCT | 115677 |
rs567435374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817215 | TGCCAGGGTATCCCC[A/C]AGTGGATAGGCAGTT | 115677 |
rs567437552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788103 | ATGACAGCCAGGCTT[G/T]GTGGTTTATACCTGT | 115677 |
rs567446598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838451 | TGCCATGTTGGCCAG[C/G]CTGGTCTCGAACTCC | 115677 |
rs567476800 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798031 | ACACACATCCTCCCA[G/T]GTACTTTAAATCATC | 115677 |
rs567514960 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818841 | TAGCATATTAAAAAA[-/T]TTTTTTTAATTTTTA | 115677 |
rs567548077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819754 | TAGTTCTAAACCCTT[C/T]GGGGTCATCAATAAG | 115677 |
rs567549506 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790446 | AGGTGAACACCATCA[A/G]TAATGGGGCAAATGA | 115677 |
rs567581541 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795730 | TTCAATGAAGTGTTA[C/T]GAGGCAAAAAGCTTA | 115677 |
rs567594053 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838953 | CATGCCCAGCTAATT[G/T]TTTGTATTTTTAGTA | 115677 |
rs567691037 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838537 | GAGCCACCGTGCCCA[A/G]CCCCAAATACTTCTT | 115677 |
rs567697711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787094 | AAGGATTCGCTGCTC[C/G]TAACAGCTGCTTCTG | 115677 |
rs567772218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814905 | ACCCATCTCTATTTT[C/T]ATAAACAAATTTTTT | 115677 |
rs567836031 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804721 | CGGGCCCACACCAAT[A/G]TACCCATGTATGGAA | 115677 |
rs567946940 | in-del | -/TCTTC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850416 | GTCAGACTTTGGGAT[-/TCTTC]TCTTGTCAAATAACC | 115677 |
rs568009913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788095 | TAGTAACGATGACAG[C/T]CAGGCTTGGTGGTTT | 115677 |
rs568058276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834406 | CGAACACAAGAGAAC[A/G]GGTTGATTCCTCCTT | 115677 |
rs568082049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839622 | CTTAAGTAAGAATAC[A/G]GGAGTCTACAGCCGG | 115677 |
rs568096335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827883 | GAGGCAGTGCCACCA[C/T]ACCTGGCCATTTCCT | 115677 |
rs568107536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799113 | GAAATTCTTGGCAAA[C/T]AACTCAGGAGCTTCC | 115677 |
rs568206489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807017 | TAATTGATTTTCATA[A/C]CTAACATTTCTAATC | 115677 |
rs568219519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862213 | AGCTCGCATAATGAT[A/G]ATAGCTAACGCTTAT | 115677 |
rs568226043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821702 | CGAGCAGCTCCTGTT[A/G]GGGATGACACAAAGG | 115677 |
rs568291657 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857540 | AGCCCCATAGACATT[C/T]GTGGGGATTGATGGA | 115677 |
rs568329177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827918 | TTTATACAGATATGA[A/T]ATAGGAAATGAAAAT | 115677 |
rs568423709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856622 | GCTCCCTTTGAGAGC[A/G]ACCGACTCCTGGCTG | 115677 |
rs568446951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862962 | TGCTATTTATTGGGT[A/G]TTTCCTTTGCAGCAT | 115677 |
rs568454627 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841725 | CCCTGAAGTTTGGCT[-/G]AAAATCACTGACAAG | 115677 |
rs568503889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822126 | CTCTCCTCTCCATCA[A/G]CTGGGACATATTCCT | 115677 |
rs568522202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789759 | GTTGCTAGTAACCTT[A/G]GGAAGCTGAAACTGC | 115677 |
rs568536299 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849222 | TCCAAAGCCTTGTTC[A/G]TGAAAGATGATTGCT | 115677 |
rs568572204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816022 | TTTTATTTTATGGCC[C/T]CTTCCACTGTTCTGG | 115677 |
rs568581632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823068 | GTCGCCCAGGCTAGC[A/G]TGCAGTGGCGCAATC | 115677 |
rs568617799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829707 | TACTTCCAGGCAACA[G/T]AATTGGGTGTTTAAT | 115677 |
rs568637527 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796656 | TTTATATCTTTTAAC[C/T]AACAAACCTCCAAGA | 115677 |
rs568720698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852146 | CATATTCTATTTGCT[A/G]GAAGCAAGTCAGTAA | 115677 |
rs568729590 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843556 | CTTGAGATGTGTACA[C/T]CTCAGTGGCAAAAGT | 115677 |
rs568729913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864147 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 115677 |
rs568755840 | snp | A/G | 0 | 0 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850929 | GACACATTCCTTCCT[A/G]GAAATCTCCCTCCAC | 115677 |
rs568793055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849598 | TGACCTCAGGTAGTT[C/T]ACCCGTCTCGGCCTC | 115677 |
rs568811211 | snp | C/T | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863465 | GCTCTTGGATCCTGA[C/T]GGGGGCAGATGATCC | 115677 |
rs568884572 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858655 | GCTTTTAGTTTTGTC[G/T]TAGGTAAGCCTGCCC | 115677 |
rs568933445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790035 | GCCCCCAGCCAGATC[A/G]AGTTAGCTCATTCTT | 115677 |
rs569002933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839060 | AAAGTGCTGGGATTA[C/T]GGGCGTGAACCACCA | 115677 |
rs569024258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810984 | AATTTATAAAGGGTA[A/C]TTAATAAATTTATAA | 115677 |
rs569044786 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865269 | CAGACGGAGTCCAAG[G/T]TGGGTTCAGCTGCTT | 115677 |
rs569082174 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864227 | CCTAATCTGCCCATC[A/G]CGGCCTCCCAACGTG | 115677 |
rs569118037 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785398 | CAGCTGAGGGTACTA[C/G]ATGGTACATAGAACT | 115677 |
rs569119365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864492 | GGTTTCACCATGTTG[C/G]TCAGGCTGGTCTCGA | 115677 |
rs569181180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790680 | GAAACTAAAGAAACA[C/T]AGTGACTGAATGCCA | 115677 |
rs569192300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791211 | TGTGTTCTCATTGTT[C/G]AATTCCCACCTGTGA | 115677 |
rs569229367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837799 | CTTAGTTAACTTCTC[A/G]GAAGTATTAAGCATT | 115677 |
rs569294779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797297 | AGATGGGGTTTTACC[A/C]TGTTGCCCAGGCTGG | 115677 |
rs569322197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859169 | CTTCGCAGACCACCA[A/G]AAATCTACCTTCTAC | 115677 |
rs569358640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796697 | AGTGGCCCCTTGGGA[C/T]TCTTGCGGAATCCTA | 115677 |
rs569404142 | snp | G/T | 0.00993419 | 0.0697739 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865639 | ATCAGGCAGGAGAAG[G/T]AAATAAAGGGCATTC | 115677 |
rs569483625 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808159 | TGTAACCCAAGCACA[C/T]AGAAAAATTCTCAAC | 115677 |
rs569530759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792689 | TTTCGCCATGTTGCT[C/T]AGGCTAGTCTGAACT | 115677 |
rs569542684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824843 | GTGCAGTGGCACAAT[C/T]ACAGCTCACTGCACC | 115677 |
rs569543514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832413 | ACAAGATTCAATGAA[A/C]CCCTCTGAGAAGACT | 115677 |
rs569583508 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800841 | TCTGAGGGCAGAGAA[C/G]CCCCCTCAAGTGGGA | 115677 |
rs569594152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798707 | ATGTAGGACCAGAGA[C/T]GAATCTGAGAACAGA | 115677 |
rs569628432 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853577 | CATGTTTAAACAATA[A/G/T]ATGTCCCCAGACAAA | 115677 |
rs569656732 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168798168 | AGATGCAGAACCCAG[A/G]GATATGGAGAGCCAA | 115677 |
rs569699897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820775 | ACCCCTTTTTCATAC[C/T]ACCAAAGCCCAACTT | 115677 |
rs569716491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859984 | AAATTATAAGATTTT[C/G]TGGTATGTATTAGTC | 115677 |
rs569718440 | snp | A/C | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864207 | TCTTGACCTCAAGTA[A/C]TCTGCCTAATCTGCC | 115677 |
rs569794077 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798633 | ATAGGAGAGGTCAGA[C/G]AGTAAATCTAACCGG | 115677 |
rs569799136 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795872 | CACTGCTTCTGCCAC[A/C]GTTTAAAGTACTCAT | 115677 |
rs569809890 | snp | A/C | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802263 | ATACAGAAAATAAAA[A/C]GCATGATTAATACTG | 115677 |
rs569827889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792033 | TTGCCATTGCTTTTG[C/G]TGTTTTAGACATGAA | 115677 |
rs569831056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833628 | CCCACTCCAAAGGGT[C/T]AGCATGAACAGGGTA | 115677 |
rs569834513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792636 | TTGTTTGTTTGTTTG[G/T]TTTGTTTTGTTTTTT | 115677 |
rs569851018 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828787 | ATAGAATAATTTGCA[A/G]TGATTCAAAATCTTA | 115677 |
rs569874537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838512 | CCCAAAATACTGGGA[A/T]TACAGGCGCGAGCCA | 115677 |
rs569877674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824401 | CTTCCCATGCTCAAG[C/T]GATTCTCGCACCTCA | 115677 |
rs569894647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805915 | GCCCACAGCCTCCCC[A/G]GTGTGCATCAGTGAG | 115677 |
rs570003478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861229 | GCTTTGTCGCTCTGT[C/T]TCCATAGCCTCCTCC | 115677 |
rs570048784 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787996 | GAGAAATACCCATGT[A/T]TGGGGGATGAGAAGA | 115677 |
rs570067601 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864340 | TGCCCAGGCTAGAGT[A/G]CAGTGGCATGATCTC | 115677 |
rs570158695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807727 | AGTATGGCTGGGAGC[A/G]AGGTACGAGGCAAAG | 115677 |
rs570199980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855247 | AAATTTTGTTTTATT[A/T]TATAAAGTTAAAATT | 115677 |
rs570220256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815633 | AAGCAATAAAAAATT[A/G]AAATTAAATATTTGA | 115677 |
rs570234646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861906 | CAAAGAGCTTCAGCT[C/T]ATATTCATTTGCCTG | 115677 |
rs570235634 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840486 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 115677 |
rs570270149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800111 | CCTGGTTAGACTACC[A/G]GCTGATGAAATACGG | 115677 |
rs570297223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807137 | GTGCTCCATGGAACC[C/T]TTTCAGAGTCCTCTC | 115677 |
rs570356455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814987 | ATGAGAAGAAGGCCT[A/T]TATTGTCCTTGGAGG | 115677 |
rs570391825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858970 | CTTTAGCTTGACTTA[C/T]TATGTTTATACTCAA | 115677 |
rs570441810 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788611 | ATGAGAAGCCAGAGC[A/G]TGGAAAGTCAGAGTG | 115677 |
rs570474816 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805161 | AAAATTTAAAAATCT[C/T]TTTTAGATCAAGCTC | 115677 |
rs570580190 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856342 | AACACTTTGGGAAGC[C/T]AAGGCGGGTGGATCA | 115677 |
rs570621385 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796256 | CAGGACTCAGAACCG[A/G]GAGTTGGCCTTCGGA | 115677 |
rs570664819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828751 | TGAAGCATTCAAAAT[A/C]AATTGTGATAAATTC | 115677 |
rs570725130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834007 | TATGCAGGAGTTCTC[C/T]GGACAAAGTGTTAGC | 115677 |
rs570828330 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849985 | CAGTAGCATGATCTC[G/T]GCTCACTGCAAACTT | 115677 |
rs570874136 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856712 | ACGAATGCTTAAAAC[A/G]TACTCCAGCACCTCC | 115677 |
rs570898584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818274 | TCCTCTCGCCTCAGC[A/C]TCTCAAGTAGCTAGG | 115677 |
rs570956018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830561 | TGGTTGAATAACGGC[G/T]GATCTGCTGGGTCTG | 115677 |
rs570961623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817717 | CGGGGCTCAGTGAGA[C/T]TCCCAAACTAGACCC | 115677 |
rs570984181 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824173 | ACAAAAGGATCCTTG[G/T]AGTAAACAAATCATC | 115677 |
rs570992882 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837057 | CTCACGTGGTGGAAA[C/G]AGAGCAAGGAAGCTC | 115677 |
rs571011623 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828105 | TAGCCAGCACATCCT[A/G/T]TTTCCTAGGAAAATG | 115677 |
rs571099459 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852567 | ATTCAGGATTTCAAG[C/T]TCCAGATTAGGGGTG | 115677 |
rs571107825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861037 | TATTTCCATTGGGAC[C/T]GATTAATTTGTTAGA | 115677 |
rs571135072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844342 | ACTATCAATTCTGGA[C/G]AGTAAGAACATGAAT | 115677 |
rs571147042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836512 | GGGGGGCATTCATTT[C/T]CTCATCTCACATAGA | 115677 |
rs571162484 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861485 | ATTAGAAATTGGTTT[-/A]AAAAAAAAAAAAAGA | 115677 |
rs571165301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802832 | GTTTTTCTTTGGTTC[A/G]GTTTAAAAACAGAGC | 115677 |
rs571173839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812210 | AGTTATGAAAGCCCT[C/G]CTTGAAATGAGAAAA | 115677 |
rs571189186 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864329 | CCTGTTGCTGTTGCC[C/G]AGGCTAGAGTGCAGT | 115677 |
rs571233301 | snp | C/T | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865490 | GGGATGGTAGGATAT[C/T]TCTGACAAACCCACA | 115677 |
rs571288210 | in-del | -/GAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788937 | GATAGATAGATAGAT[-/GAT]AGATATTTCATAACT | 115677 |
rs571308494 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785320 | TAATTGGAGCTATGT[C/T]ACCAAAGATGAGTTC | 115677 |
rs571330880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831291 | TATAAGGGCACTAAT[C/G]TCATTCATGGGGGCT | 115677 |
rs571372177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838396 | AGGCGTGCGCCATCA[C/T]ATCTGGCTAATTTTT | 115677 |
rs571413663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803955 | GTTTTTGTATAGGGG[C/T]GGCAGGCCAGGACAG | 115677 |
rs571449597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851826 | TAGTTTATGTGGGTC[A/G]GGAATTCAGTTGTGT | 115677 |
rs571461565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860593 | GGAGAATCACTTGAA[A/C]CCGGGAGGTGGAGGT | 115677 |
rs571468451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851491 | AATTGAAAGCAAATA[C/T]CATGTTTTATCAATG | 115677 |
rs571550029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860133 | TTTCTAAGGCTCAAG[A/G]GCTCGAAAACAATCT | 115677 |
rs571586830 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865814 | CATCACAAGCATTCT[C/T]ATATACACCAATAAC | 115677 |
rs571613439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832457 | TTGAAATCCTTTTTC[A/G]TCTCCAAAGCGTTAG | 115677 |
rs571686465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791913 | AGTAGGTGGCAAAAA[A/T]TTTCTCCCATTGTGT | 115677 |
rs571716555 | in-del | -/AGAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788933 | GATAGATAGATAGAT[-/AGAT]GATAGATATTTCATA | 115677 |
rs571751001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791235 | CCTGTGAGTGAGAAC[A/G]TGCGGTGTTTGGTTT | 115677 |
rs571792532 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791684 | TTAATGATCACCATT[C/G]TAACTGGTGTGAGAT | 115677 |
rs571808460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797378 | TTGAGATAACAGGCA[C/T]GAGCTGCCACACCCA | 115677 |
rs571839362 | snp | G/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785895 | AGCTGGAATTACAGG[G/T]GCATGCCACCACACC | 115677 |
rs571920202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819575 | GTTTCGTTATAACTG[C/T]GCAGAAAGAGTGCAC | 115677 |
rs571989309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794072 | CTGTCATAGAGTAAT[A/G]TAACCTTCCTTCATC | 115677 |
rs571996811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833241 | CTAATGAAAAGCCTT[A/G]AAGGACCAAATATTC | 115677 |
rs572003971 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795578 | TTTCTCCATTAACAC[C/G/T]TGGAGTTTTAAAATT | 115677 |
rs572049833 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786720 | GGCCCTCCTCGAAGT[C/G]TACTTTACTTCCTTT | 115677 |
rs572062108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839173 | TCCCCATTCTCCGTC[A/G]TAAGCTGTGTGATCC | 115677 |
rs572153754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797720 | TGGTGGTTCACTTCT[C/G]TAATCCCAGCACTTT | 115677 |
rs572190122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845714 | GTAACAAGGTATACA[C/T]TCATTTACATTTCAA | 115677 |
rs572298452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835130 | CCCAGGCTGGAGGGC[A/G]GTGGTGCAATCTTGG | 115677 |
rs572306381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825715 | AAGATAGTTCATTCG[C/T]GGTAATTTGCTACAA | 115677 |
rs572308495 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842227 | GCCTCAGGGGAGAAT[G/T]GGAGTGAGAGACAGG | 115677 |
rs572335432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834493 | TCATTACTGGCGTGC[A/G]CGCGCGCGCGCGCGC | 115677 |
rs572517012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862626 | CTCAGAAAAGCTTTT[C/T]ACAGCCAGTCTAAAG | 115677 |
rs572604352 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790993 | TTGTTTTCTTTTTTT[-/A]AATTTTATTATTATT | 115677 |
rs572616195 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792327 | AGTGAAAGAAAAAAA[-/T]GCATTAAATAAAACT | 115677 |
rs572699701 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844739 | GCCGCGCGTGGTGGC[A/G]GGCGCCTGTTGTCCC | 115677 |
rs572699898 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788178 | CCAGGAGTTCAAGGC[C/T]GCAGTGAGCTATGAT | 115677 |
rs572762469 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793758 | ATCTGGCCTCTGAGT[A/G]TCTTCCAAGCCTCAT | 115677 |
rs572785587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808823 | CAATTAGGATCCCAA[C/T]GGGGATTTAAAAAGA | 115677 |
rs572817090 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821870 | GAGGCTGCCGGAGTC[A/G]GATCATGCAGAGCTT | 115677 |
rs572855940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828018 | AATGTAATCTCATAG[A/T]GAAATTGAAATAAGG | 115677 |
rs572881985 | snp | A/G | 1.81023e-05 | 0.00300846 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851420 | GTGAGTATGAAATGG[A/G]AAAAAAAAGTTACAT | 115677 |
rs572894199 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857079 | CCCAGTTAAGAAAAG[C/T]GACAGGAAACAAAGG | 115677 |
rs572904748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841682 | CTGTGTTACCTATGT[C/T]AGGGCCAAGGGAAAT | 115677 |
rs572922193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789820 | ACCGAGAAACAAAGG[A/G]CCTTCAAGAAGCTTT | 115677 |
rs572964648 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801908 | TCTTGATCCTGTTGG[A/G]GCTGGAGCGAGTGTG | 115677 |
rs572983191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789449 | AAACCATCAGATCTC[A/G]TGAGACTTATTCACT | 115677 |
rs572994025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849028 | GAATTAACAACACAG[A/G]GATATAGAGGAATAC | 115677 |
rs573092331 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812805 | CAGAGAGAGGGGCAG[A/G]GTGTGTCCCTTTGTT | 115677 |
rs573120655 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852982 | AATCTATTTTCTTAC[A/G]AAGAATAATAAAAAT | 115677 |
rs573193036 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850639 | AAGGCCTGGCTAGGC[A/G]CGGTGGCTCATGCCT | 115677 |
rs573208029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808009 | TGCCACTGAAGGCAA[C/T]TGAGTTTTCAATCAC | 115677 |
rs573240584 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825940 | ATTTTTAGGACAGTA[C/T]TTTAGTAGACTACAG | 115677 |
rs573304269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829343 | CTTTCTTTTTTTGAC[A/G]GAGTTTTGCTCTTGT | 115677 |
rs573306565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794955 | TTCAAAAGTGCAAAA[A/G]GAAATCCAGTAAAGA | 115677 |
rs573370781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803247 | CTACCAAAAATATAA[C/G]TTTGGTCAGAAGTCC | 115677 |
rs573391188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836017 | CAGCACCACTGCAAA[C/T]CCCTTACAAAGGAAG | 115677 |
rs573435600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811257 | TTTTTGTCCTTCCTG[A/G]GAACAATAGGGGTGA | 115677 |
rs573448147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857686 | CTGTGATTAGAGATC[A/C]TGAGTGGACTGGGGT | 115677 |
rs573450736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823687 | CCTATTCCCATATGA[C/G]GTCACATTCACAGGC | 115677 |
rs573486540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857016 | TCTAAAATAGTATTC[G/T]CCAAACAGAGTCGTT | 115677 |
rs573488730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864245 | GCCTCCCAACGTGCT[A/G]GGATTACAGCTGTCA | 115677 |
rs573519754 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803254 | AAATATAAGTTTGGT[C/T]AGAAGTCCAAAGACA | 115677 |
rs573567902 | snp | C/G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840182 | CTGTTGCCAGGTTAA[C/G/T]GTTCACAAGCTTGAG | 115677 |
rs573601818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843760 | AACAAGAATTATTGT[A/G]CCCCTGTAGGGGGAA | 115677 |
rs573619859 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837586 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACCGCG | 115677 |
rs573629089 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851536 | TACCCCATATAAATT[A/T]AAAAAACCCAGCATT | 115677 |
rs573708241 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859361 | TTTATTCCTCCATTT[G/T]TTTTTCCTTCGGCAT | 115677 |
rs573748540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824597 | AGCCACTGTGCCCAG[A/C]CCAGTACATCCTATT | 115677 |
rs573838912 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786004 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 115677 |
rs573866774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790891 | AGGAGCATTAGATTG[A/G]CAACTTATTCAGGAC | 115677 |
rs573928406 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791238 | GTGAGTGAGAACATG[C/T]GGTGTTTGGTTTTTT | 115677 |
rs573981293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852972 | CAATAAAATAAATCT[A/C]TTTTCTTACAAAGAA | 115677 |
rs574035940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819227 | CCTCCCTTTGAGAGA[G/T]GAGAAGAAATCATTC | 115677 |
rs574118658 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787609 | CCTTACCTTTTATAG[C/G]TGATCCTTATCAGCC | 115677 |
rs574139826 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799677 | TAGAGTCTTTTATGA[A/T]TTAGGTCCTCTTATT | 115677 |
rs574186041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798312 | TGCCAATTCTTTGCA[C/T]GCTTTGGCTACTAAA | 115677 |
rs574223022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845830 | TCCAAGTCACATGGA[A/G]TATCTACTCATCATA | 115677 |
rs574285781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806591 | GGGTTATTATTTTTT[C/T]AGGGGCTCAGGAAGA | 115677 |
rs574418048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813330 | CAAAATTAGTGCCTG[A/G]TAGAGAGCTGTGAAG | 115677 |
rs574479005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826500 | TTCCATTTTTACCCT[C/G]TCTTTTCACAGGTGT | 115677 |
rs574506653 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812702 | GGAAGGTAAATATAC[C/G]GGAAGAGTAAAGTCT | 115677 |
rs574517559 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825831 | GGGGAAAGGAAAAAA[A/G]GAAGGCTTCTGGAGC | 115677 |
rs574519572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833818 | CTTAAAACAATCTCA[A/G]ATCGTGGCCTAGGTT | 115677 |
rs574539365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815194 | AAAGTACAGTTGTTA[C/T]TAAAACACTCTTTTG | 115677 |
rs574605890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833288 | TTTCCCAGCAGGCAT[G/T]TGGCTGACGGGAGGT | 115677 |
rs574614665 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820897 | CCTTGTACAGTCTGC[A/C]AGAACATTCTGAAAG | 115677 |
rs574625458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807411 | AATGATTGATTCTAA[A/G]TAAGGGTTTATGCTG | 115677 |
rs574630898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814389 | TTCCTCCTCTAGATA[C/T]ACATTGGATAGAAGG | 115677 |
rs574654845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854681 | CAGCCCTTTGCTCCC[A/G]CCATTTTTCCTGCCT | 115677 |
rs574670148 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853408 | CCATAAATGCCATGT[G/T]CAAAAGATTGTTATC | 115677 |
rs574674069 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836966 | TCAACAGCAGACATT[C/T]TGGAAGTGTGGGATC | 115677 |
rs574682532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820382 | GAATGACGCCTGGCA[C/T]GTTGTAAGTGCCCAG | 115677 |
rs574688903 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829020 | TTTATACTTTTTTGC[A/G]TTTTTAAAATAATTT | 115677 |
rs574725385 | snp | A/C | 6.63306e-05 | 0.00575855 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828136 | ACACTCACCTTTGTT[A/C]CCCACTTTTTTTTGC | 115677 |
rs574774638 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796190 | ATGCAGTGACAACAG[A/G]GAACGCTGCTGCTCC | 115677 |
rs574780369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860962 | ACTGGCAGGGCACAT[C/T]GCTACATTTAAATTT | 115677 |
rs574785882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793777 | TCCAAGCCTCATGAA[C/G]TATAAGGTCCCATGC | 115677 |
rs574862423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856842 | ATTTTTAGAATACTT[A/G]TTTCTGGTCCACTTG | 115677 |
rs574862903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847458 | GAGGGGTCTAGATAT[C/T]CTAAAGTTTGAGAGT | 115677 |
rs574864099 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811510 | AGGTGCTCTATCTTC[A/G]GAGTTGCTCGTAATC | 115677 |
rs574936573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848116 | TTTTCTATAGGGTAA[A/G]GACTTCTTCTTTTTG | 115677 |
rs574945704 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819795 | AGAAAGGGTACAATC[A/G]TGCTGTTCAGAGAGG | 115677 |
rs574950317 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823140 | TCCTGCCTCAGCCTC[C/T]TGAATAGCTGGGACT | 115677 |
rs575004507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822418 | TTCATTTTATAGAAG[A/G]GGGCTGTCTTTCTTT | 115677 |
rs575009199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835773 | CCACAACTGTCCATG[A/T]GTGAGCACCAGTGTA | 115677 |
rs575035675 | in-del | -/AAAGGGCATTCAATTAGG | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865643 | GCAGGAGAAGGAAAT[-/AAAGGGCATTCAATTAGG]AAAGGGCATTCAATT | 115677 |
rs575077615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794245 | TGTAAAATGCTACAG[A/G]GAGGCAAAATGAAAG | 115677 |
rs575124420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788302 | CCTTTTTCTTTTTCC[A/G]TTCCTTTCCCTTCTC | 115677 |
rs575125615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809360 | AAAACCTTCCCTCAC[A/G]TCTCCTTGGATAGCT | 115677 |
rs575245246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863157 | CTTATACTTTATATT[C/T]TAAGCAGTTTCTTTA | 115677 |
rs575294506 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835250 | CGGCTAATTTTTTTT[C/T]GCATTTTTAGTAGAG | 115677 |
rs575308041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836628 | GAAGCTGATCTAAAC[A/C]TCCGTTCTCCTCACA | 115677 |
rs575404005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809556 | AAATCTAGTGGAAAT[A/G]TTTAGGTAACATAGG | 115677 |
rs575433316 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841559 | TCAAGCTGTCCATAA[A/C]TTGCAGTGAACATTG | 115677 |
rs575514088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795925 | TTTTTTTCTTCCATC[C/T]TGAGGCTGTGGGCAA | 115677 |
rs575519334 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832144 | TGGGGTCCACTTTTT[A/G]TGCACAACACTATTC | 115677 |
rs575577396 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802568 | TGAATCCCGGAAGTC[C/T]AGGACACACCCAACC | 115677 |
rs575674093 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842959 | CTTTCAAAAATGTGT[G/T]AGTAAATGTGTGACA | 115677 |
rs575683884 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803956 | TTTTTGTATAGGGGC[A/G]GCAGGCCAGGACAGG | 115677 |
rs575742769 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823279 | CCTCGGCCTCCCAAA[A/G]TGCTAGGATTACAGG | 115677 |
rs575785399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812004 | ATTTTTCTCTCCCCT[C/T]GAAGGGCAGAGGCAG | 115677 |
rs575801914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811370 | AAAAGTTCTCCTGGG[A/T]CTTTCATATCCAGGT | 115677 |
rs575809196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819336 | AGGATACATATACTG[C/T]CTCATTAGACCGGAA | 115677 |
rs575831807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830197 | ATATGATAGTCATTA[A/G]CATTTCTTTAGTATT | 115677 |
rs575863379 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817951 | GGTCTTTCAAAAGAC[A/G/T]TACCAATGAAGTTTG | 115677 |
rs575878372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851643 | CAGAATCTTCATATT[C/T]GGTCTTCTATAAAAG | 115677 |
rs575879829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864312 | CTGAGACAGAGTCTT[A/G]CCCTGTTGCTGTTGC | 115677 |
rs575888257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864686 | TTATACACAGGTGTT[C/T]GATACATTTGGCTTC | 115677 |
rs575918005 | snp | C/T | 8.30034e-05 | 0.00644165 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851254 | TTTCTTCGACAACCT[C/T]ATTCTGTTCCCCTTG | 115677 |
rs575982324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845971 | GCTTCTCCTACCCCA[A/C]CTTCCTCTGAGTTCT | 115677 |
rs576001325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837600 | AGGCGTGAGCCACCG[C/T]GCCCGGTCACAATAT | 115677 |
rs576004039 | snp | G/T | | | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826565 | AGTGAGGGCCAGAGA[G/T]TCTTCCAAGGTCATG | 115677 |
rs576171471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786702 | CCCTCAAGTGGCCAG[C/T]TTGGCCCTCCTCGAA | 115677 |
rs576188879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852045 | CTCAGCCTACTCCCC[A/G]CAAAATGAGTGATCA | 115677 |
rs576190861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844604 | AGATTCAGCCTGGGC[A/G]GCACGCCTGTAATCC | 115677 |
rs576191111 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839743 | AGATGGTGAAATCCT[C/G]GGCGTGGTGGCACAT | 115677 |
rs576193929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833202 | TTCAGCATGTCAGTA[A/G]TGAAGTAGTCTATTT | 115677 |
rs576308222 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832733 | AGTATCCAGTCATTT[C/G]CTTTTTAGTTTTGCC | 115677 |
rs576324745 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791421 | GGTTGGTTCCAAGTC[G/T]TTGCTATTGTGAATA | 115677 |
rs576324945 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841692 | TATGTCAGGGCCAAG[A/G]GAAATCTTCCCTTTT | 115677 |
rs576350216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814101 | GACACAAATATTCTA[C/T]TAATCTATGAATTTG | 115677 |
rs576366639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860708 | CAGAAAAAACAACTT[A/G]AGGAAAACAGCTACA | 115677 |
rs576540514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833976 | CCTCTTGAGGGTACC[C/T]GATATAATGAAAAAG | 115677 |
rs576596568 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856586 | TCTTAAAAAAAAAAA[-/T]CTCACTGGTATCACT | 115677 |
rs576596663 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829948 | GGAGAAATGATTTTT[A/G]AAAATTTTATTCAAA | 115677 |
rs576624902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839113 | TCATGTGGCCTGTAA[A/G]ACCCTTCCTGACTTG | 115677 |
rs576632332 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853947 | ATGTCAGCTCACTGC[A/C]ACCTCTGCCTCCCGG | 115677 |
rs576706031 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832247 | TTCTAGGAGGAATTA[C/T]GATCTGGCGTGGGAA | 115677 |
rs576729470 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821406 | GTAAGAATTCCAACC[-/A]AAGACCTGGTGGGAA | 115677 |
rs576739876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861684 | ATGCATGCAATTACT[A/T]TTATTATACAATGAT | 115677 |
rs576827163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794895 | ACTGCACCTGGCTCT[C/T]AGTAAATACTTTTTA | 115677 |
rs576834487 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798458 | TCATGTTGTTAACTC[C/T]CCTTAGAGGCAGCAC | 115677 |
rs576905923 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820972 | TTTCCTGTTAAAAAC[C/T]ATTCAGGATTGTTCT | 115677 |
rs576908366 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835703 | ACACAGTGAGGGCCT[A/C]GGGCAGCTTTTCAGG | 115677 |
rs576914793 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797621 | AATAACATGTCATCA[C/T]CTCAACTGTCAGTTC | 115677 |
rs576950782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827046 | GGCATCTTTTGGTCT[A/G]GTTCTCTTATTCTTA | 115677 |
rs576954269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807945 | TTGGTCCAGCAGCCC[C/T]TTACTTTAAGAGGTT | 115677 |
rs577005702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855699 | ACCTATATAAGTATT[A/G]TACTACTATTTTCAG | 115677 |
rs577018416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807516 | TGGGGGAATTTTTGG[C/T]GTATAGTATATAGGA | 115677 |
rs577081805 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815257 | GCTTCTTTTATCCAA[G/T]TAGCTACCTCAGCTT | 115677 |
rs577085074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822520 | CCCAAATGAAATAAC[A/G]TAATAAATAATTCTA | 115677 |
rs577099400 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806530 | CATTTTCCTAATGGC[C/T]GAATGGGAAATGTCT | 115677 |
rs577100874 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789131 | AAAGGCTGGGTGTGG[A/G]ACATCTTTTTGGGCC | 115677 |
rs577169228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842928 | CATATAATTATTACT[A/G]TGGAATTACAAAGGG | 115677 |
rs577173136 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788804 | CATGTATGGTTTTTA[A/T]TAAGTAGATATCAAA | 115677 |
rs577245524 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823322 | CGCCCGGCCAGTTGC[A/T]TTAGTTTTTAGGGCT | 115677 |
rs577405044 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837552 | CTGACTTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 115677 |
rs577480826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863767 | GACATACTTATAGCA[A/G]CCAACACGCCAAACA | 115677 |
rs577509592 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829012 | ATTTCATTTTTATAC[-/TT]TTTTGCATTTTTAAA | 115677 |
rs577530078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843638 | TATGTCAGCAAGCAC[A/C]TCACAAAAGGAGAAA | 115677 |
rs577553696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811172 | GTCATGAGCCCCAGA[A/T]ATATTATTTTGAAGT | 115677 |
rs577556073 | snp | A/G | 0.000100928 | 0.00710307 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802612 | CCAGAATGCTGGAGC[A/G]TAGGTGAAAGGACAA | 115677 |
rs577581210 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865168 | GGTGGAGACAGACAA[C/G]GAAGAGGCTCCTTGG | 115677 |
rs577610179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850334 | CACAAAATAAAGAGG[A/C]TATGTGTCTACCTGC | 115677 |
rs577610671 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857518 | TTGTGCTGAGTGTGT[C/G]AACTCTAGCCCCATA | 115677 |
rs577616557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810386 | AGGGACCTGGATTAC[C/T]TCATTTCTTTAGGTC | 115677 |
rs577676570 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838204 | CCATCACTTTTTTTC[C/T]ACCAAAGATAATCTT | 115677 |
rs577714159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789245 | TAAAATTAATAAGCT[C/G]GTGTATTAGTTTGTT | 115677 |
rs577792413 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839619 | TTCCTTAAGTAAGAA[C/T]ACAGGAGTCTACAGC | 115677 |
rs578019793 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795960 | CGAAACCCTTAAAAA[A/T]TTTTTTTTAAAATAT | 115677 |
rs578169798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851711 | ATCACTGTATATCAC[A/G]TGGTGCTTAAATTGG | 115677 |
rs578185282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845053 | GGGGAAATTAAAGGA[A/G]AGATGAAAACTTGGG | 115677 |
rs578202519 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857707 | GGACTGGGGTTAATC[-/TG]AGAATCATTTAAGGA | 115677 |
rs578243418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812534 | AATACATGCTATACC[C/T]ATCACATGGGAGAGG | 115677 |
rs578247582 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860596 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGT | 115677 |
rs745319752 | snp | G/T | 1.65685e-05 | 0.00287819 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864914 | AAAGGCCATTTTCCT[G/T]CCGCTTATGTGGAGG | 115677 |
rs745322516 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811169 | TTTGTCATGAGCCCC[A/C]GAAATATTATTTTGA | 115677 |
rs745342387 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809301 | CATTTTCAAGTCCAG[A/G]AGGAAGAAAAGAGGG | 115677 |
rs745351179 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854011 | TAGCTGTGATTACAG[A/G]TGCACACCACCACGC | 115677 |
rs745387501 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820589 | TGAAGATTTCTAAGG[A/T]ACTTGTCTGTAAAGA | 115677 |
rs745398413 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864419 | GCCTCCTGAGTAGCT[A/G]GTATTACAGGCGTGC | 115677 |
rs745407796 | snp | A/C | 3.32105e-05 | 0.00407482 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864988 | CAAGACTCTGAACAT[A/C]CTACCTTCACACTCG | 115677 |
rs745485642 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790376 | ATATTTACTAACTTC[A/G]AAGGTTAAAGTAGTG | 115677 |
rs745490998 | snp | C/G | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851099 | AGCATTCTGGAGCTG[C/G]AGAAGGAAAGAATTC | 115677 |
rs745560419 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859283 | AAGGTTTCCTGTTCA[-/C]CCCCAGAGTACAGAA | 115677 |
rs745579185 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819775 | CATCAATAAGTTGCA[A/G]GCAGAGAAAGGGTAC | 115677 |
rs745599019 | snp | A/G | 1.6674e-05 | 0.00288734 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859688 | TGGGCCTGCTGGGTG[A/G]AGTGGCTTAAAGTAG | 115677 |
rs745616507 | in-del | -/AAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843580 | CAAAAGTAGACACAT[-/AAA]GAAGGAATTGTGGCA | 115677 |
rs745658730 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831546 | TAAGGCAAGTATCCA[C/G]AAATACCATTTGTGT | 115677 |
rs745672578 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827803 | AGTTTTGAACCTGTG[A/G]CCTCAAGTGATCATC | 115677 |
rs745688904 | snp | G/T | 1.65704e-05 | 0.00287836 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860833 | AATATCTCGGCCTTT[G/T]TTAATGAAGAGATTA | 115677 |
rs745815222 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798267 | CCATAAAGTATTTAA[C/T]TAGGTCTCAATTGAT | 115677 |
rs745827532 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852242 | GGAGTCACTATCAGT[A/G]TTTTTCATGGTCCCT | 115677 |
rs745843475 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796940 | CACTCTCTCAGTATT[C/T]AATTCAATCAAATGA | 115677 |
rs745874215 | snp | G/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862016 | TTGTATTCTTTTCAA[G/T]CCAGGCAAGATGATG | 115677 |
rs745898721 | in-del | -/AAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840531 | GAGACTCCATCTCAA[-/AAAAAA]AAAAAAAAAAAAAAA | 115677 |
rs745907975 | in-del | -/AC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807270 | CACACACACATACAT[-/AC]ACACACACACAGAGA | 115677 |
rs745932380 | snp | C/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856608 | GGTATCACTTCTAGG[C/G]TCCCTTTGAGAGCGA | 115677 |
rs745987625 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790389 | TCAAAGGTTAAAGTA[A/G]TGACTCTACAGCGAA | 115677 |
rs746040286 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861443 | TTCAAGTATAATTAC[C/T]ATAATCTTGACTATC | 115677 |
rs746073791 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794666 | CAGCGGATGATTTTT[A/C]ACAAGTACTCAGAGG | 115677 |
rs746077981 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840636 | AATTGGAATAATAAA[C/G]TGAATGGTATTAACG | 115677 |
rs746094861 | snp | A/T | 1.65781e-05 | 0.00287902 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861936 | GCTAACACAGCATAC[A/T]AATTACAGCTTTATC | 115677 |
rs746143240 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806430 | CCTGTCTAAACATTT[A/C]ATGTGCTGACTGGCT | 115677 |
rs746157279 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837460 | GACTACAGGCCCCGC[C/T]ACCACACCCAGCTAA | 115677 |
rs746157523 | in-del | -/A | 0.0001628 | 0.00902073 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855895 | ACGTAGAAGTTAGGC[-/A]TGTCAGACTGTGAAG | 115677 |
rs746181287 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168801149 | CTTTGGATAAGCAAA[C/G]AGGGAGGGCATTAAG | 115677 |
rs746215701 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168846968 | TAATTTCCTTTCTAT[A/G]AAAGTGTCTTGAGGA | 115677 |
rs746246784 | snp | A/G | 1.79197e-05 | 0.00299325 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834352 | TGGCTGGCTGGGCGC[A/G]TGTGCCATAGAGAGG | 115677 |
rs746366520 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801508 | GATTACATGCATGAG[C/T]CACTGCAACTGGCTT | 115677 |
rs746390416 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797741 | CCAGCACTTTGGGAG[A/G]CCAAGACAGATGAAT | 115677 |
rs746405418 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827953 | TGAAAAATAACTGGG[-/A]AAAAAAGCAGTATAT | 115677 |
rs746415410 | snp | C/G | 1.66671e-05 | 0.00288674 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834223 | TGTATGTTTTTTACT[C/G]TAGGCCAAGAAGAAA | 115677 |
rs746420870 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825636 | TTCTTTTCAATATAT[C/T]GCAGCACTAAGAATG | 115677 |
rs746428245 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814282 | ACAATTATGTTGGTT[A/G]TGGTTGTTAAACCAT | 115677 |
rs746453400 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798438 | AATACTTCATAAATG[C/T]GTACTCATGTTGTTA | 115677 |
rs746463912 | snp | A/G | 3.31713e-05 | 0.00407242 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856695 | TCATTTTCAGGCCTG[A/G]AACGAATGCTTAAAA | 115677 |
rs746501938 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798082 | TAATGCTATGTAAAC[A/G]TTATATAAATAGTCA | 115677 |
rs746541239 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854950 | ATGTCTTCCACTCCT[A/G]AGGCAGTCATAGCCT | 115677 |
rs746553338 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841489 | GATGGGCAAGAGGGG[G/T]GCTCTTTGTAAGGGA | 115677 |
rs746642408 | snp | C/G | 1.65932e-05 | 0.00288034 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828126 | TAGGAAAATGACACT[C/G]ACCTTTGTTCCCCAC | 115677 |
rs746663353 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811105 | TACCAGGTTATTTAC[C/T]GACAGTTTCATATCT | 115677 |
rs746720868 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822273 | GTTTTCTGCAGCTAG[A/G]CCTTAGCATACATCC | 115677 |
rs746763481 | snp | G/T | 4.96899e-05 | 0.00498422 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851109 | AGCTGGAGAAGGAAA[G/T]AATTCAACTTTTATG | 115677 |
rs746770610 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835878 | CAGGAACAAAATGAA[A/C]ATTTTCTGCTTACAC | 115677 |
rs746781843 | snp | C/G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805543 | ATTAATAGCACCTTC[C/G/T]TATCAAACAATCACA | 115677 |
rs746786783 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849849 | GCTTAGTTGCTAAAG[C/G]TTTCTGCCCCCTGTA | 115677 |
rs746855695 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861150 | ATCAGATGACTGGCA[A/T]CCACCTTATTCAAAT | 115677 |
rs746891951 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813609 | CATTCACTTATTCTA[-/G]AGTGACAAACATATC | 115677 |
rs746913119 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854752 | TCTTCTTGCCTCCTC[A/G]AAGCTGTCAGCTGCC | 115677 |
rs746926239 | snp | A/C/G | 5.10776e-05 | 0.00505338 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856626 | CCTTTGAGAGCGACC[A/C/G]ACTCCTGGCTGTGTC | 115677 |
rs747076897 | in-del | -/CTC | 3.31351e-05 | 0.00407019 | cds-indel, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856733 | CAGCACCTCCTCCTT[-/CTC]TGATGCAAAGAGCCA | 115677 |
rs747087083 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858779 | GGTTGGGAATTCCCA[C/T]GCTGGAGGTGTGGGG | 115677 |
rs747093002 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825791 | CCATTGTAGAGGTCT[C/T]TTTTGATGATGAAAG | 115677 |
rs747094695 | snp | C/T | 1.65963e-05 | 0.0028806 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828479 | ATCAAGTCCTAAATG[C/T]ACAAGAGAAGAAGAG | 115677 |
rs747169222 | snp | C/T | 3.31631e-05 | 0.00407191 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864831 | CTAACTGTATTTTCA[C/T]AGGTGACATTGTGAT | 115677 |
rs747249185 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839289 | GAGATCGATTTTTGA[C/G]CACTTACTATGAGCC | 115677 |
rs747253072 | snp | C/T | 3.45083e-05 | 0.00415367 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855347 | ATCCTTCTTTTTTCC[C/T]AAAGGAAGAAGATCC | 115677 |
rs747288799 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824443 | AGCTGGGATTATAGG[C/T]GCCTGCCACCACGCC | 115677 |
rs747380889 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801257 | GTTGTTTCTGGAAGC[-/T]TTTTTTTTTTTTTTT | 115677 |
rs747422147 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862042 | TGATGAGTTGAATTT[C/G]GAAAAGGGTAAGAAT | 115677 |
rs747445138 | snp | G/T | 1.83061e-05 | 0.00302535 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834364 | CGCATGTGCCATAGA[G/T]AGGGATGGACTTGCT | 115677 |
rs747469836 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804058 | GCAATGGACAGAAGA[C/T]AGGGAAATGGTGGGC | 115677 |
rs747499463 | snp | A/T | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860837 | TCTCGGCCTTTTTTA[A/T]TGAAGAGATTAGAGA | 115677 |
rs747531141 | snp | A/G | 1.98014e-05 | 0.00314647 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802634 | AAAGGACAAAAGCCA[A/G]ACACATTTCAACATG | 115677 |
rs747567579 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816668 | TCTCAAAAAAATGTT[C/G]CTCAGTTCTATGTGT | 115677 |
rs747569817 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830900 | TTACACATGATTGCA[C/T]ATGTTTACATGCTTT | 115677 |
rs747573858 | snp | C/G | 1.65927e-05 | 0.00288029 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843034 | GAAAAGTTGGAAAAG[C/G]AAGATGAAAATTACT | 115677 |
rs747600062 | snp | C/T | 1.89874e-05 | 0.00308113 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834375 | TAGAGAGGGATGGAC[C/T]TGCTGCCCTTAGCTA | 115677 |
rs747605613 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802647 | CAGACACATTTCAAC[A/T]TGAGGGACCCACTGA | 115677 |
rs747689924 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827551 | ATTTTATTTTATTTT[-/C]ATTACTTATTTTTTT | 115677 |
rs747862188 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856216 | GAAGAGAAAGGTAAA[C/G]AGTTCATTTATCATT | 115677 |
rs747871103 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812577 | AGTATTTCTCTCTCA[A/G]GGCAGTGGCTTAGGG | 115677 |
rs748081126 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818381 | AGGCTGGTCTCAAAC[C/T]CTTGGTCTTAATGAT | 115677 |
rs748092188 | snp | A/G/T | 3.31836e-05 | 0.00407319 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851230 | GCCTGGTAAGAAGGG[A/G/T]CAGAAACCTTTCTTC | 115677 |
rs748182518 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804316 | CCTTGTCTAAAACTT[C/T]GAAGGTCATCTGTAT | 115677 |
rs748227147 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848090 | AAACAGAAGAGCTGA[A/T]TTCTAGATCTTTTTC | 115677 |
rs748291910 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836723 | CACAGCCACCTGCCT[A/G]CTGAAGTAATAGCAT | 115677 |
rs748351263 | snp | C/G | 1.67573e-05 | 0.00289454 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855446 | ACATTGAAAAAGCCT[C/G]AAAAGACAAGGAAGG | 115677 |
rs748372159 | snp | A/G | 1.66233e-05 | 0.00288295 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828491 | ATGTACAAGAGAAGA[A/G]GAGAAAATCAGTGAG | 115677 |
rs748381424 | snp | A/G | 3.32082e-05 | 0.00407468 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831488 | TTGACAATGAAGTTG[A/G]AAAGACAGCAAATCT | 115677 |
rs748396475 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855037 | GTAAATAAGGAAGCA[A/G]TAAGTATACAACAAA | 115677 |
rs748426244 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811379 | CCTGGGTCTTTCATA[C/T]CCAGGTAGAAGAGAC | 115677 |
rs748432096 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816151 | CAGAAATCTAATCCA[C/T]TCTTACCCCTTAAGC | 115677 |
rs748499806 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819201 | TTTTCAGCTTGAACC[A/G]AGATAAAGCACCTCC | 115677 |
rs748524890 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822592 | AAAACTCTTAGGATC[G/T]ATATTAAAAAGGAAA | 115677 |
rs748543503 | snp | A/T | 1.65658e-05 | 0.00287795 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864884 | GGATGGTGGTTTGGA[A/T]CTTTGAATGGGAAAA | 115677 |
rs748547642 | snp | A/C | 1.68218e-05 | 0.00290011 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855362 | TAAAGGAAGAAGATC[A/C]TAACAGTGCAATGGA | 115677 |
rs748557500 | in-del | -/TGAGGA | | | intron-variant, cds-indel | NOSTRIN | GRCh38.p7 | 2:168863388 | TAGAAAGAAAGTTGC[-/TGAGGA]TGAGGAAAAGAGTGA | 115677 |
rs748608260 | snp | A/C/T | 6.63695e-05 | 0.00576029 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843065 | ACCAAAAAAACATGG[A/C/T]GGGTTATTCTACCAG | 115677 |
rs748633996 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864745 | ACCAAGTAAATCCTT[C/G]AAGCAGAACCTCCTT | 115677 |
rs748656871 | in-del | -/G | 1.65729e-05 | 0.00287857 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828150 | TCCCCACTTTTTTTT[-/G]CCTTTAGTTGTGTTA | 115677 |
rs748686146 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789403 | CGTGGCTGCAGGCAA[A/G]AGGGCTTGTATAGGG | 115677 |
rs748722343 | snp | C/G | 1.95716e-05 | 0.00312816 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811637 | GCAAACAGGTCACAT[C/G]TGTTCTTCAGCAAAG | 115677 |
rs748759171 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819675 | AGGTTCCCAAAATGG[C/T]CATTAGGATTTAAAA | 115677 |
rs748774826 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804577 | GCAAATGAGTGCCTC[A/G]TGAAACATTTAGGTA | 115677 |
rs748784808 | snp | A/G | | | intron-variant, missense, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863407 | GGAAAAGAGTGAAAG[A/G]AAGACTGAAAAATCA | 115677 |
rs748799918 | snp | A/C | 2.10773e-05 | 0.00324626 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811657 | CTTCAGCAAAGGTAC[A/C]AAATGCACGTTTGCA | 115677 |
rs748814356 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832248 | TCTAGGAGGAATTAC[A/G]ATCTGGCGTGGGAAG | 115677 |
rs748857963 | snp | C/T | 1.66131e-05 | 0.00288206 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843069 | AAAAAACATGGCGGG[C/T]TATTCTACCAGACTG | 115677 |
rs748875287 | snp | A/G | 1.65732e-05 | 0.00287859 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864848 | GGTGACATTGTGATT[A/G]TACACGAGAAAAAAG | 115677 |
rs748915384 | snp | G/T | 8.31e-05 | 0.00644539 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859670 | TGGTTGTAATTTCTT[G/T]ATTGGGCCTGCTGGG | 115677 |
rs748943907 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802371 | CTTCTCTCAATGTTA[C/G]GCTGTTCAGGACTCA | 115677 |
rs748995380 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801486 | GCTCGGCCTCCCAAA[C/G]TGCTTGGATTACATG | 115677 |
rs749024505 | snp | G/T | 2.15366e-05 | 0.00328144 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850914 | GATTTAAGATACCAA[G/T]ACACATTCCTTCCTG | 115677 |
rs749064043 | snp | A/G | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859551 | GAAGCGAACTCCTAC[A/G]AACTGTCATCAATGT | 115677 |
rs749133522 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839494 | TGACACACGGAAGGC[C/T]CTCAATGTCTGGTGA | 115677 |
rs749201436 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828268 | CCAAAGGGAATCAAA[C/T]ATTTAAAGTGGGTTT | 115677 |
rs749235162 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809005 | ATTATTTTCTGTATC[A/G]TTATGTTATGAAACA | 115677 |
rs749269514 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817382 | GGTTTGTGGGGAGCC[C/T]ACAGGGGCTACCTCA | 115677 |
rs749275104 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820349 | GGATTAAATGAGGAA[A/C]TATACCTATAACACC | 115677 |
rs749280116 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787411 | CTTCTTCTTCATGTC[A/G]CTAACTCTTACTTGG | 115677 |
rs749289733 | snp | A/C | 1.65894e-05 | 0.00288 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828471 | ACCGACTTATCAAGT[A/C]CTAAATGTACAAGAG | 115677 |
rs749301829 | snp | C/G | 1.65685e-05 | 0.00287819 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860867 | AATATTGTGAGCAAG[C/G]CATCTTCTGGTGGGC | 115677 |
rs749323390 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806204 | AAGGCAGTCAGCAAA[A/G]TTCATTGTGTTAAAT | 115677 |
rs749353439 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835822 | GAGTAAGCTTGACAA[C/G]TGTGTTTTCAGGCAA | 115677 |
rs749361016 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837206 | AGAAAGTTACAGGAA[C/G]ACTTATTTATGGGGT | 115677 |
rs749372445 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838450 | TTGCCATGTTGGCCA[C/G]GCTGGTCTCGAACTC | 115677 |
rs749393282 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849390 | AGATGGAATCTCACT[C/G]TTTTGCACAGGCTGG | 115677 |
rs749395436 | snp | A/G | 6.63196e-05 | 0.00575807 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861930 | TTGCCTGCTAACACA[A/G]CATACTAATTACAGC | 115677 |
rs749448235 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861047 | GGGACCGATTAATTT[C/G]TTAGACTCTGTAGCT | 115677 |
rs749457679 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805488 | AAGGCGAAGTAAGAT[A/C]CAATTATCTCTAAGG | 115677 |
rs749497034 | snp | G/T | 7.23353e-05 | 0.00601352 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834187 | CTCTTGGCATCAGCC[G/T]CTGCTCCTTTTTTTC | 115677 |
rs749616522 | snp | G/T | 1.70087e-05 | 0.00291617 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855466 | GACAAGGAAGGTGTG[G/T]AACCATCTCTTTGAA | 115677 |
rs749621593 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824124 | TCTGTCTTTTTAGGA[A/T]CCTCTTGGATACCCT | 115677 |
rs749641687 | in-del | -/TTA | 3.32331e-05 | 0.0040762 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828410 | TGTGTCTTTTATGTT[-/TTA]TTTCCAGAAAACTTG | 115677 |
rs749704321 | snp | A/C | 3.31895e-05 | 0.00407353 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831507 | GACAGCAAATCTTGT[A/C]ATTAGCAACTGGAAT | 115677 |
rs749709026 | in-del | -/A | 1.75437e-05 | 0.00296168 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851437 | AAAAAAAGTTACATT[-/A]ATGGAGAATCTTAGG | 115677 |
rs749772037 | in-del | -/TATATGTGTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839918 | ATATATATATATATA[-/TATATGTGTG]TGTGTGTGTGTGTAT | 115677 |
rs749819304 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794541 | TGTTTTTACTAGAGA[C/G]GGGGTTTCACTGTGT | 115677 |
rs749825107 | in-del | -/GTGT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857387 | GAATAGGGCAGTCTG[-/GTGT]GTGTGTGAGGCAAAA | 115677 |
rs749866364 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823393 | GAAGTGTGTTGTCTC[A/G]CAGTTCTGCAGGCTG | 115677 |
rs749899068 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836580 | TCAGCAAATTCTTCC[G/T]GGTTTCCTGCTCAGC | 115677 |
rs749916041 | in-del | -/GTCCCGAGATCT | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802481 | TTCTCGGGACACAAA[-/GTCCCGAGATCT]CGGGATGAAAGTCCA | 115677 |
rs749923661 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865056 | GTGCTCTTACCTTTA[A/C]ATGTTTTTCTTTTGA | 115677 |
rs749960006 | snp | A/T | 6.64275e-05 | 0.00576276 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851293 | GTGCCACACGCAGAT[A/T]CACTGTGCCATCAGC | 115677 |
rs749998025 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814381 | GTCAGAAATTCCTCC[C/T]CTAGATATACATTGG | 115677 |
rs750015182 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792250 | TAAAATGAGGATGCC[A/G]TCTATGACTTTCAAG | 115677 |
rs750104420 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835591 | GATATTTGTGCATTT[G/T]GTGTATGTTAACCTA | 115677 |
rs750111672 | in-del | -/AT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856585 | TCTTAAAAAAAAAAA[-/AT]TCTCACTGGTATCAC | 115677 |
rs750115963 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803953 | ATGTTTTTGTATAGG[C/G]GCGGCAGGCCAGGAC | 115677 |
rs750147107 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817557 | TGCCTTTCTTGTCCA[-/C]CTTTACCTGAATTCC | 115677 |
rs750158413 | snp | A/G | 0.000165629 | 0.00909873 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861971 | TCAGCCCCTGGTGCA[A/G]CCCAGCTCAGCAGCA | 115677 |
rs750163703 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813432 | TCTCTGCTTGAAGCC[C/T]GTCTCACTGTTTTTC | 115677 |
rs750281419 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856347 | TTTGGGAAGCCAAGG[C/T]GGGTGGATCACAAGG | 115677 |
rs750312423 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823631 | AGGGTTTGGGCCCAC[C/G]CTGATGACCTCATCT | 115677 |
rs750339804 | snp | A/G | 1.66457e-05 | 0.00288489 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831468 | CTTTTTCCTTTTTCA[A/G]TAGCTTGACAATGAA | 115677 |
rs750353478 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820895 | CACCTTGTACAGTCT[G/T]CAAGAACATTCTGAA | 115677 |
rs750358110 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812174 | CTGTGCTGAAATGAG[C/T]ACATTTAACTCAGTC | 115677 |
rs750393305 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793972 | GTTGGATACCTCTTT[A/G]TAATTCCCATTACAT | 115677 |
rs750445151 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854871 | CATAAACCCATTCTG[G/T]AAAGAGCATATGTGT | 115677 |
rs750480935 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852529 | ATTCTGATAGCGTTT[-/C]CCTGGGTCCTCTGCC | 115677 |
rs750488244 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864455 | CACACCCAGCTAATT[C/T]TTGTATTTTTAGCAG | 115677 |
rs750499275 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842518 | AAATAATATCGCTAG[A/G]TAGGACAGTAGCCAG | 115677 |
rs750527777 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852136 | GACATCTCATCATAT[C/T]CTATTTGCTAGAAGC | 115677 |
rs750550170 | snp | A/C | 1.66158e-05 | 0.0028823 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864802 | ATGTGTTCACATCAC[A/C]GAGACCCATTTGTCT | 115677 |
rs750626575 | in-del | -/CACACGCG/CACACGCGCG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834513 | GCGCGCGCGCACACA[-/CACACGCG/CACACGCGCG]CACACACACACACAC | 115677 |
rs750636280 | snp | C/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859587 | GAACTTGAGCAAAGA[C/G]CTCAACCCAGCCATC | 115677 |
rs750671532 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807601 | CTAAATTAACAACAA[A/G]TATGAAGATCTTCTC | 115677 |
rs750695017 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833224 | AGTCTATTTGGGAGA[C/T]TCTAATGAAAAGCCT | 115677 |
rs750710394 | snp | A/G | 1.65946e-05 | 0.00288046 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802699 | CAGTGTGGTTTGTGT[A/G]CCTGCGTGTGAGGAG | 115677 |
rs750725565 | snp | A/T | 1.74509e-05 | 0.00295384 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843150 | ATTTTTTTCTTCTTC[A/T]GTGGAGCTTTGTGTG | 115677 |
rs750735538 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816454 | CCTTACTGGGCCACT[A/T]GCAATCCCACCCCAT | 115677 |
rs750742668 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807938 | CTGTGCTTTGGTCCA[A/G]CAGCCCCTTACTTTA | 115677 |
rs750758442 | snp | A/G | 1.65811e-05 | 0.00287929 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859497 | TGCTCACATGGCCAA[A/G]TGATGTATCCACAGA | 115677 |
rs750761302 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829544 | CAGGCTTGTCTCCAA[C/T]TCCTGACCTCAGGTG | 115677 |
rs750781712 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859883 | TTTTGATTTCTTCTT[C/T]CTCATCATACCTGAA | 115677 |
rs750791844 | in-del | -/AGTT | 1.65704e-05 | 0.00287836 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864929 | CCGCTTATGTGGAGG[-/AGTT]AGTTACCTTCAAATG | 115677 |
rs750856347 | snp | G/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785010 | AATGGAAGCGATCTA[G/T]GTAGTAACGCTAGTT | 115677 |
rs750889779 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832722 | GTCCCAGAAACAGTA[C/T]CCAGTCATTTGCTTT | 115677 |
rs750897079 | snp | A/G | 1.65655e-05 | 0.00287793 | splice-donor-variant | NOSTRIN | GRCh38.p7 | 2:168828221 | AGCGGACCTGCATCA[A/G]TGAGTTCTCCCACCC | 115677 |
rs750909217 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797388 | AGGCATGAGCTGCCA[C/T]ACCCAGCCTAAACTA | 115677 |
rs750923479 | snp | C/T | | | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826911 | CCAAGCAACCACTGA[C/T]CTGCTTCCTGTCAAT | 115677 |
rs750928254 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796526 | CTCTTAGATGTTCTT[C/G]GCAAACTTGTCAGAA | 115677 |
rs750994789 | snp | A/T | 1.65671e-05 | 0.00287807 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856756 | CAAAGAGCCAGAAAG[A/T]CACAGCAGCGTTAAT | 115677 |
rs751008033 | in-del | -/AGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788925 | GATAGATAGATAGAT[-/AGA]TAGATAGATGATAGA | 115677 |
rs751021167 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823871 | CACCTGAGGTCAGGC[A/G]TTTGAGACCAGCTGA | 115677 |
rs751036077 | snp | A/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856118 | TTGCTAGAATGGGTC[A/G]ACTGAAAGAATTTCA | 115677 |
rs751125938 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789265 | ATTAGTTTGTTCTCA[C/T]GCTGCTAATGAAGAC | 115677 |
rs751131579 | snp | A/G | 1.65847e-05 | 0.0028796 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828447 | AGCAATTGAATTGGA[A/G]GCAATAAAACCGACT | 115677 |
rs751137357 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794111 | GTCCTTGAAAGAAGG[G/T]ATTGGCACTTGTTCC | 115677 |
rs751162272 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849645 | ATAGGCATGAGCCAC[A/C]GCACCTAGCCAGGCC | 115677 |
rs751164118 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823288 | CCCAAAATGCTAGGA[A/T]TACAGGCGTGAGCCA | 115677 |
rs751190702 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805896 | ATGGCATGGGTGTCA[C/T]GTGGCCCACAGCCTC | 115677 |
rs751206157 | snp | G/T | 3.32353e-05 | 0.00407634 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851307 | TTCACTGTGCCATCA[G/T]CAAGATTGACATTGA | 115677 |
rs751228530 | in-del | -/TTC | 1.71796e-05 | 0.00293079 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843141 | TATATTCACATTTTT[-/TTC]TTCTTCTGTGGAGCT | 115677 |
rs751239579 | snp | A/C | 6.93109e-05 | 0.00588648 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851425 | TATGAAATGGAAAAA[A/C]AAAGTTACATTAATG | 115677 |
rs751256103 | snp | G/T | 1.65869e-05 | 0.00287979 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861910 | GAGCTTCAGCTCATA[G/T]TCATTTGCCTGCTAA | 115677 |
rs751259993 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831846 | TGGGCAATGGAGACA[A/C]AGAGAGTTTCAGTAA | 115677 |
rs751275335 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841236 | CCAGACCCTGTCTCC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAGAA | 115677 |
rs751295551 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802195 | TAGCTAACCCTCAGA[A/G]AGGCAGTCTGTCTCC | 115677 |
rs751295732 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787956 | GCTTTGATCTGTTCT[G/T]CACTGCCTGCCAAAG | 115677 |
rs751379384 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845673 | GCATCATGGAAATTA[-/TC]TCTTTTCTTACAGTC | 115677 |
rs751404443 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861978 | CTGGTGCAGCCCAGC[C/T]CAGCAGCAGACTTTG | 115677 |
rs751419865 | in-del | -/GTC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797614 | ATACAAAAATAACAT[-/GTC]ATCATCTCAACTGTC | 115677 |
rs751440564 | in-del | -/CAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860689 | AAAAAAAAGAAAAAA[-/CAAA]CAGAAAAAACAACTT | 115677 |
rs751443864 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814875 | GTTTGAGACCAGCCT[A/G]TTCAACAAAGCACAA | 115677 |
rs751471330 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801017 | CCCAAAGTGCTAAGA[C/T]TACAGGTGTGTGCCA | 115677 |
rs751538896 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818222 | GCAGTGGTGCAATTA[-/T]AGCTTGCTGCAGCCT | 115677 |
rs751555129 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857065 | CATGTGCACTTTAAC[C/G]CAGTTAAGAAAAGCG | 115677 |
rs751556129 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842309 | GCCTTGATTTTGTGG[A/T]ATTGTTTTCTGAGTC | 115677 |
rs751569041 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844321 | TAAATATGACCAAAT[A/T]AAATAACTATCAATT | 115677 |
rs751584598 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB, cds-indel | NOSTRIN | GRCh38.p7 | 2:168846851 | CCAAGGATGGCACTT[-/GAG]TAGTCCCACTCTAGA | 115677 |
rs751627099 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797758 | CAAGACAGATGAATC[A/G]CTGGAGTTCAGGAGT | 115677 |
rs751693122 | snp | A/C | 1.67304e-05 | 0.00289222 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855437 | TGCAGAGAGACATTG[A/C]AAAAGCCTCAAAAGA | 115677 |
rs751705231 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823990 | TAAGGCAAAAGAATC[A/C]CTTGAACCTGGGAGG | 115677 |
rs751718907 | snp | A/G | 1.65756e-05 | 0.00287881 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864948 | TACCTTCAAATGCTG[A/G]CAACACAGCTACAAA | 115677 |
rs751735676 | snp | C/G/T | 3.52956e-05 | 0.00420081 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851041 | GTGACTTCCATTTTG[C/G/T]ATAACAACTGGCTGA | 115677 |
rs751807553 | in-del | -/CATTAGC | 3.31868e-05 | 0.00407336 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831507 | GACAGCAAATCTTGT[-/CATTAGC]AACTGGAATCAGCAA | 115677 |
rs751823320 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810369 | GTTCCATCCCCAAAG[A/G]TAGGGACCTGGATTA | 115677 |
rs751866656 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817967 | TACCAATGAAGTTTG[G/T]ATAGAAAATATCAGC | 115677 |
rs751881126 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804928 | TTACAGTTGTTGCAC[A/C]TATCTAGAAATATTT | 115677 |
rs751927623 | snp | C/G | 0.000309981 | 0.0124457 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850815 | CTTTTCTTCTTTTCT[C/G]CCCCTTCCTCATAAA | 115677 |
rs751962464 | in-del | -/AC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807271 | CACACACATACATAC[-/AC]ACACACACACAGAGA | 115677 |
rs752003865 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834400 | TAGCTACGAACACAA[G/T]AGAACGGGTTGATTC | 115677 |
rs752029071 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809988 | AAAAAAATCATGTTT[C/T]GGATGCAAATCCTGA | 115677 |
rs752061213 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817402 | GGGCTACCTCAGGGG[G/T]TGAGGAGGAGGTTAA | 115677 |
rs752086504 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786384 | ATCAGCAGCGTCCCA[A/G]TAAGATCTCAGGTGT | 115677 |
rs752143458 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799152 | TTCTTTTCCTTTGAA[A/G]ACCTACTTGTACCTG | 115677 |
rs752171697 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858119 | TTGGGTTATACATCT[A/G]TTCCTTTGGCTGTCC | 115677 |
rs752183055 | snp | A/G | 1.65652e-05 | 0.0028779 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859617 | CCTTGTAGTAATTCC[A/G]TCTTCAGGTGGAGGG | 115677 |
rs752186264 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815288 | CTTTTTTTGCAGTAG[C/G]AAACAGATTTAGCCA | 115677 |
rs752189148 | in-del | -/A | 1.65712e-05 | 0.00287843 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864857 | GTGATTATACACGAG[-/A]AAAAAGAAGGAGGAT | 115677 |
rs752216389 | snp | G/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857093 | GCGACAGGAAACAAA[G/T]GATCTGCATTCAGAA | 115677 |
rs752240367 | in-del | -/T | 1.65941e-05 | 0.00288041 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851239 | GAAGGGGCAGAAACC[-/T]TTCTTCGACAACCTT | 115677 |
rs752294445 | snp | C/T | 1.66738e-05 | 0.00288732 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855406 | AAGTCTTTACTAAAA[C/T]CAAAATTATTGAGAC | 115677 |
rs752328173 | snp | C/G | 1.6859e-05 | 0.00290331 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831439 | TAAACAAGAAGAAAG[C/G]AAAGCTTTGTTTCCT | 115677 |
rs752342728 | snp | A/C | 1.65864e-05 | 0.00287974 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828464 | CAATAAAACCGACTT[A/C]TCAAGTCCTAAATGT | 115677 |
rs752354162 | in-del | -/CT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817558 | TGCCTTTCTTGTCCA[-/CT]TTACCTGAATTCCCT | 115677 |
rs752376010 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795613 | GAAATTTGGACATGC[A/G]TAATAAAAATTAAAC | 115677 |
rs752448285 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823945 | CCGGGCATTGTGGTA[C/T]GTGCCTGTAATCCCA | 115677 |
rs752484714 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839280 | ATTCATATGGAGATC[A/G]ATTTTTGAGCACTTA | 115677 |
rs752546485 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803214 | CCATGTTTGTTCGTT[C/T]TGGTAATGTTTGGAG | 115677 |
rs752560609 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863314 | GTCCTTTAAGAATAG[G/T]GATTTATGACTAAGA | 115677 |
rs752604497 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817128 | ACATACTTCTCTCCA[C/T]TTCTGATTTACAGAT | 115677 |
rs752642063 | snp | A/G | 3.89446e-05 | 0.00441257 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802677 | ACAGATTGTCCGGTG[A/G]GTAGCTCAGTGTGGT | 115677 |
rs752697906 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861019 | TCTGTTTAAGGAAAT[C/T]TATATTTCCATTGGG | 115677 |
rs752702282 | snp | G/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802318 | GCACTGTCAGACCAA[G/T]CGCAAGAATTGTTGG | 115677 |
rs752715731 | snp | A/G | 6.62932e-05 | 0.00575693 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860826 | ATGTGAAAATATCTC[A/G]GCCTTTTTTAATGAA | 115677 |
rs752750053 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826220 | TGCCTCCTAAGGAAT[-/G]AGGGGTGTAGGGGTG | 115677 |
rs752831079 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829382 | CTGGAGTGCAATGGC[A/G]TCATCTTGGCTCACT | 115677 |
rs752831161 | snp | A/G | 1.66813e-05 | 0.00288797 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831578 | AACTCAGTTTTTAGA[A/G]TTGAAGTGTTTTGCT | 115677 |
rs752877246 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858954 | GAGACTAGGAGTGTA[A/T]CTTTAGCTTGACTTA | 115677 |
rs752883888 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797971 | TCAAAATCCAAAGAT[A/G]TTCAAGTCCCTTATA | 115677 |
rs752932696 | snp | A/T | 1.65941e-05 | 0.00288041 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864974 | ACAAAGGCATAAAAC[A/T]AGACTCTGAACATAC | 115677 |
rs753001501 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807222 | TGATTTCACCCCCAC[A/G]AAGCAGGTAAGTTCC | 115677 |
rs753026536 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842451 | GGACCAGGACTCTTA[C/T]CCTGGAAGTTTGATT | 115677 |
rs753028694 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855802 | CAACCAACTGTGCAT[A/G]AGAGTTTTGGATGAG | 115677 |
rs753068629 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838062 | GATAAATAATACATA[C/G]TCAATAAGTATATTC | 115677 |
rs753183264 | snp | A/C/T | 8.84867e-05 | 0.00665108 | intron-variant, missense, stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850911 | AGTGATTTAAGATAC[A/C/T]AAGACACATTCCTTC | 115677 |
rs753185153 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803261 | AGTTTGGTCAGAAGT[C/T]CAAAGACATTGTGAG | 115677 |
rs753229873 | snp | G/T | 1.65913e-05 | 0.00288017 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860808 | AGGAGCATACTCATA[G/T]CTATGTGAAAATATC | 115677 |
rs753263723 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787205 | GCATTTGAGACAAAG[A/G]GCATAGCGTGAAGCA | 115677 |
rs753271123 | snp | A/G | | | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862044 | ATGAGTTGAATTTGG[A/G]AAAGGGTAAGAATCA | 115677 |
rs753305215 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846743 | CTGCAATATGTGTCA[A/G]GAGCCTTAAAAATAT | 115677 |
rs753342851 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803400 | TTATCCCAACACATG[G/T]GGCTGAAAAGCTAAG | 115677 |
rs753405451 | snp | G/T | | | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859566 | AAACTGTCATCAATG[G/T]TAGCAGAACTTGAGC | 115677 |
rs753447477 | snp | A/C | 1.66344e-05 | 0.0028839 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831552 | AAGTATCCACAAATA[A/C]CATTTGTGTAAACTC | 115677 |
rs753537026 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816373 | TATAAAAGGGCCTTC[A/G]AGAGCTGAACTCTGC | 115677 |
rs753572865 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822988 | GTAGGACAGTTTTCT[A/G]TTCCTTACTAGTTGT | 115677 |
rs753594046 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815413 | TCTCAGAAACACTTT[A/G]TGAATGTTTGGCTTC | 115677 |
rs753600226 | snp | C/T | 1.65756e-05 | 0.00287881 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860822 | AGCTATGTGAAAATA[C/T]CTCGGCCTTTTTTAA | 115677 |
rs753642432 | snp | C/G | 1.66852e-05 | 0.0028883 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831460 | TTTGTTTCCTTTTTC[C/G]TTTTTCAATAGCTTG | 115677 |
rs753734990 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791562 | GATCCCTGAGGAATT[A/G]CCACACTGTCTTCCA | 115677 |
rs753751695 | snp | C/G | 1.85115e-05 | 0.00304227 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855320 | ACTCTTACTTCTTCC[C/G]CCTTGTTAGACATCC | 115677 |
rs753801845 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819198 | ACTTTTTCAGCTTGA[A/T]CCGAGATAAAGCACC | 115677 |
rs753837467 | snp | A/G | 1.6698e-05 | 0.00288941 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855426 | ATTATTGAGACTGCA[A/G]AGAGACATTGAAAAA | 115677 |
rs753841280 | in-del | -/G | 9.427e-05 | 0.00686484 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824767 | CTTTTTTTATTTGTT[-/G]TTTTGTTTGTTTGTT | 115677 |
rs753859502 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804596 | AACATTTAGGTAGTT[G/T]TATAAAAGAACCCAA | 115677 |
rs753884391 | in-del | -/TT | 0.000117886 | 0.00767652 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860775 | GTTACAAAATATGAC[-/TT]TTTATGTCATTTGAA | 115677 |
rs753939675 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862207 | AACAAAAGCTCGCAT[A/G]ATGATAATAGCTAAC | 115677 |
rs753944995 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861038 | ATTTCCATTGGGACC[A/G]ATTAATTTGTTAGAC | 115677 |
rs753965174 | snp | C/T | 2.02587e-05 | 0.0031826 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802603 | TTACAGTGTCCAGAA[C/T]GCTGGAGCGTAGGTG | 115677 |
rs753976439 | snp | A/G | 1.6727e-05 | 0.00289193 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842987 | ACATTGATGTTTTAC[A/G]TTAGCTCCTCAATAA | 115677 |
rs753982193 | snp | A/G | 6.62712e-05 | 0.00575597 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856751 | TGATGCAAAGAGCCA[A/G]AAAGACACAGCAGCG | 115677 |
rs754042093 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786551 | ACTGCGCATGCAGCC[C/T]TTCCCAAGCACTGGT | 115677 |
rs754069753 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787685 | GAATATGCATTTACA[A/G]AAAGAGGAGCTGTGA | 115677 |
rs754093960 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800580 | CCACTGGGAATGGCA[A/C]ACATGAGGAGTTTGG | 115677 |
rs754100994 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839801 | TGAGGCAGGCGAATC[A/G]CTTGAACCTGAGAGG | 115677 |
rs754105978 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831710 | CCAAACCAATGGAAG[G/T]GCATGGCTCTAACTA | 115677 |
rs754160959 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830760 | CAGGGGTAATGGAGA[C/T]ACACAGTAAAACTGG | 115677 |
rs754234432 | in-del | -/ATCCTCTAAG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835566 | AGGTTCTTGGCAGAA[-/ATCCTCTAAG]ATCCTCTAAGATATT | 115677 |
rs754242488 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849188 | CTTCTTCCCTATGGT[C/T]GTGTTACCCACCAAC | 115677 |
rs754321337 | snp | A/G | 3.314e-05 | 0.00407049 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851191 | GACCACAGTGAGTAG[A/G]GATGATCTCTCCATT | 115677 |
rs754340029 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808286 | GTAACTTCTATGTGC[A/G]GACTATCCTGTGGTG | 115677 |
rs754372560 | in-del | -/TGAA | 3.31307e-05 | 0.00406992 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864888 | GGTGGTTTGGATCTT[-/TGAA]TGGGAAAAAAGGCCA | 115677 |
rs754410024 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813752 | TACAAAGCACATTCC[C/T]GCACAAAAACAGTAT | 115677 |
rs754473721 | snp | C/T | 1.6585e-05 | 0.00287962 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828458 | TGGAAGCAATAAAAC[C/T]GACTTATCAAGTCCT | 115677 |
rs754502890 | in-del | -/T | 0.000488092 | 0.0156143 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828141 | ACCTTTGTTCCCCAC[-/T]TTTTTTTTGCCTTTA | 115677 |
rs754528029 | snp | A/C | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856150 | AATCTCATCTGGAAA[A/C]ATAACAATCAAGATG | 115677 |
rs754551962 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812508 | AAAAGAAAAACAAGC[A/G]GAAACTTATTAATAC | 115677 |
rs754560643 | in-del | -/T | 0.000170809 | 0.00923987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850797 | TTGTGTCTCAAATGC[-/T]TCCTTTTCTTCTTTT | 115677 |
rs754588507 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823295 | TGCTAGGATTACAGG[C/T]GTGAGCCACCGCGCC | 115677 |
rs754619424 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839214 | AAAAATATCTTTCTG[C/T]ATCCTGCCATACTAT | 115677 |
rs754642185 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865159 | AGATGGATGGGTGGA[G/T]ACAGACAAGGAAGAG | 115677 |
rs754665591 | snp | A/C | 1.65682e-05 | 0.00287817 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828234 | CAGTGAGTTCTCCCA[A/C]CCTGGCCTTTCTCCA | 115677 |
rs754683622 | snp | C/G | 6.62526e-05 | 0.00575516 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861985 | AGCCCAGCTCAGCAG[C/G]AGACTTTGCAAGGCC | 115677 |
rs754754333 | snp | A/G | 1.65866e-05 | 0.00287976 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851223 | CTGGTATGCCTGGTA[A/G]GAAGGGGCAGAAACC | 115677 |
rs754773687 | snp | A/G | 1.66203e-05 | 0.00288268 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851312 | TGTGCCATCAGCAAG[A/G]TTGACATTGAAAAAG | 115677 |
rs754794731 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819325 | GGAATCCTGAAAGGA[C/T]ACATATACTGCCTCA | 115677 |
rs754803046 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802244 | AAGGTCAAAGCATCA[C/T]ACAATACAGAAAATA | 115677 |
rs754886847 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845232 | ATCTGGCTCTGCAAC[C/G]TGGGCTCTGATCTTG | 115677 |
rs754897108 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796798 | CATTTTAGAGTTCCT[G/T]CCCAGAAGGTCACAC | 115677 |
rs754907067 | snp | A/T | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856654 | GTCCCACTGAGACAG[A/T]GTGAAAGGTGACTGA | 115677 |
rs754937173 | snp | A/T | 2.03056e-05 | 0.00318628 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802599 | TTGATTACAGTGTCC[A/T]GAATGCTGGAGCGTA | 115677 |
rs754949541 | snp | A/C | 1.65913e-05 | 0.00288017 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861918 | GCTCATATTCATTTG[A/C]CTGCTAACACAGCAT | 115677 |
rs754964579 | snp | A/C | 1.67326e-05 | 0.00289241 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855440 | AGAGAGACATTGAAA[A/C]AGCCTCAAAAGACAA | 115677 |
rs755040473 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827056 | GGTCTAGTTCTCTTA[C/T]TCTTAGACTGCAGGA | 115677 |
rs755041883 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816720 | TGTAGCTCTTACACC[C/G]TGCACTGTAATTCTC | 115677 |
rs755054570 | snp | C/T | 1.6643e-05 | 0.00288465 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831469 | TTTTTCCTTTTTCAA[C/T]AGCTTGACAATGAAG | 115677 |
rs755064363 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822073 | TTCATCAAGGGTGAT[-/G]GGTCTCTCCCAGCTG | 115677 |
rs755074279 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829222 | CGATCCTCTACTCTT[C/T]CTCTGTGCCTTTCCT | 115677 |
rs755127257 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842346 | TGTGCCTGAATTCTC[A/G]AAGCAACCCGGTATG | 115677 |
rs755211949 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810408 | CTTTAGGTCTTTCCT[C/T]CTCTGTCACCCTATG | 115677 |
rs755252390 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821660 | GATCCTTTTTTAGAC[A/G]GGGCAAACCTCTGAG | 115677 |
rs755254556 | snp | C/T | | | intron-variant, missense | NOSTRIN | GRCh38.p7 | 2:168846884 | TGAGACGAATGACAA[C/T]TCATTACATAAAATG | 115677 |
rs755255348 | snp | C/T | 1.65652e-05 | 0.0028779 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864875 | AAAGAAGGAGGATGG[C/T]GGTTTGGATCTTTGA | 115677 |
rs755306415 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796661 | ATCTTTTAACCAACA[A/G]ACCTCCAAGAAAGTT | 115677 |
rs755311455 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805964 | CACATTTCTTGGACC[A/T]CTGTTTCCTTGTGTG | 115677 |
rs755378135 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836848 | TTCCCATATCTTGGA[C/G]AGCCCACTCCCTAAT | 115677 |
rs755390021 | snp | C/T | | | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860863 | AGAGAATATTGTGAG[C/T]AAGGCATCTTCTGGT | 115677 |
rs755414046 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817433 | GTGGGCAGGGCTCTG[C/T]TTCCTCCTCATTCCT | 115677 |
rs755419665 | snp | A/C | 1.92143e-05 | 0.00309948 | stop-gained, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811623 | TGGAGAGAATTTCTG[A/C]AAACAGGTCACATCT | 115677 |
rs755428776 | in-del | -/AA/ACACACAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834514 | CGCGCGCGCACACAC[-/AA/ACACACAT]ACACACACACACACA | 115677 |
rs755431463 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848925 | GATGCCTAAGGTGGA[C/T]AAAATGGCATGTCAT | 115677 |
rs755489701 | snp | G/T | 1.65902e-05 | 0.00288008 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843046 | AAGGAAGATGAAAAT[G/T]ACTACCAAAAAAACA | 115677 |
rs755494417 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847982 | ATGCTAGTGGTTCAG[C/T]ACTTGTCAAAGTAAA | 115677 |
rs755510709 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860045 | TAATGCATCAGTACA[C/G]CTCTGAAATGCTTGT | 115677 |
rs755579448 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786420 | AAGTGGGCTCAAGCA[C/T]GCGCACTATGAGGCA | 115677 |
rs755605972 | snp | A/G | 1.65729e-05 | 0.00287857 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859628 | TTCCATCTTCAGGTG[A/G]AGGGAAAAGGTAACA | 115677 |
rs755615339 | snp | A/C | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860811 | AGCATACTCATAGCT[A/C]TGTGAAAATATCTCG | 115677 |
rs755628463 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830352 | CCCACCACCCCACTC[C/T]ACTCTCTCACAAAAT | 115677 |
rs755630891 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858330 | CACATGATTTCATTA[C/T]GCATGCTCTGCATCT | 115677 |
rs755672615 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790636 | AATGGCAGGAAAGCC[A/G]AGGAGGAGCTAAGAA | 115677 |
rs755672811 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845362 | TCCCACTCCATCTTC[A/C]AGGCACCCACCCTTC | 115677 |
rs755688570 | in-del | -/TG | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864821 | ACCCATTTGTCTAAC[-/TG]TATTTTCACAGGTGA | 115677 |
rs755715302 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815318 | AGAGAAACATAGCAG[C/G]TCCTAGAATGCCTAA | 115677 |
rs755726893 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856251 | CAAATTTATTAAGAA[C/G]TACCTGCAGAGACTC | 115677 |
rs755753145 | snp | A/C | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857101 | AAACAAAGGATCTGC[A/C]TTCAGAAAGGCCTGT | 115677 |
rs755762558 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825102 | ACATGTTCCATTCCA[G/T]CTTCCTCTTCTAAAC | 115677 |
rs755782007 | snp | C/T | 1.68168e-05 | 0.00289967 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831444 | AAGAAGAAAGCAAAG[C/T]TTTGTTTCCTTTTTC | 115677 |
rs755806164 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791316 | GTCCCTATAAAGGAC[A/G]TGAACTCATCCCTTT | 115677 |
rs755861431 | snp | A/G | 3.53163e-05 | 0.00420201 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851445 | TTACATTAATGGAGA[A/G]TCTTAGGTACTGAGG | 115677 |
rs755870165 | in-del | -/AGT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848694 | AGATGCAAAAGAACA[-/AGT]AGTAGTGTATGATTC | 115677 |
rs755891339 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844390 | CCCACCTGTTTTAAG[-/T]TTTAAAAAAAAAATG | 115677 |
rs755904856 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808899 | ATAGCCAAATAAATT[A/T]TGAAAAGGAAAAAAA | 115677 |
rs755907660 | snp | A/C/T | 4.97585e-05 | 0.00498771 | stop-gained, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828465 | AATAAAACCGACTTA[A/C/T]CAAGTCCTAAATGTA | 115677 |
rs755950598 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819447 | TAACAGCTTTCTTCA[C/T]GCTTGCCACTTGGAA | 115677 |
rs755972226 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820251 | ATGTGCCCTCAGGCT[A/G]GTGACTGACCCAACT | 115677 |
rs755984556 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852284 | CCTTGGACCAGATTA[C/T]CGGAGGCTTATTTTG | 115677 |
rs756051303 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861007 | CTTTGACCTGTATCT[C/G]TTTAAGGAAATTTAT | 115677 |
rs756055765 | snp | C/T | 3.32546e-05 | 0.00407752 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851319 | TCAGCAAGATTGACA[C/T]TGAAAAAGATATCCA | 115677 |
rs756061995 | snp | C/T | 1.66283e-05 | 0.00288338 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864796 | TGAGGCATGTGTTCA[C/T]ATCACAGAGACCCAT | 115677 |
rs756075395 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863351 | AGAAAAGATAGAAAA[C/G]GAGTTAATAATTTCC | 115677 |
rs756110490 | snp | A/T | 1.67044e-05 | 0.00288997 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831579 | ACTCAGTTTTTAGAA[A/T]TGAAGTGTTTTGCTT | 115677 |
rs756153854 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805322 | GAACTTATTTGAAAA[A/G]GATATCTGTAAGATA | 115677 |
rs756153856 | snp | A/C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800502 | CCCAGTGGCAGACAG[A/C/G]AGCAAGATGGAAGGA | 115677 |
rs756220687 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848820 | TTGTTTCATGGGTAC[A/G]GTTTACTTTTGCAAG | 115677 |
rs756226003 | snp | C/G | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856748 | CTCTGATGCAAAGAG[C/G]CAGAAAGACACAGCA | 115677 |
rs756250973 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830591 | GTGTTCCAGGGAAAA[A/C]CATTCTGCTGTAACT | 115677 |
rs756381301 | in-del | -/CACACACA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834507 | GCGCGCGCGCGCGCG[-/CACACACA]CACACACACACACAC | 115677 |
rs756384953 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797288 | TTTTGGTAGAGATGG[C/G]GTTTTACCATGTTGC | 115677 |
rs756422134 | snp | G/T | 1.69415e-05 | 0.00291041 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856639 | CCGACTCCTGGCTGT[G/T]TCCCACTGAGACAGT | 115677 |
rs756423667 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795644 | CCTATTACACTGACT[A/G]TAAGACAGTTTTGCA | 115677 |
rs756469011 | snp | A/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785483 | AAGTCATTTCTGAGG[A/T]GTTATAAAATAGTTT | 115677 |
rs756474487 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794501 | GGACTACAGGTGCCC[A/G]CCACCGCGCCTGGCT | 115677 |
rs756480148 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838113 | TCTATGCTGGCAATA[C/T]CCAAATTTATATCTC | 115677 |
rs756522311 | snp | A/C | 1.65658e-05 | 0.00287795 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864885 | GATGGTGGTTTGGAT[A/C]TTTGAATGGGAAAAA | 115677 |
rs756536592 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824017 | GAGGTGGAGGTTACA[C/G]TGAGCCAAGATTGTG | 115677 |
rs756577475 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856348 | TTGGGAAGCCAAGGC[-/G]GGTGGATCACAAGGT | 115677 |
rs756601575 | snp | A/G | 1.96709e-05 | 0.00313609 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811639 | AAACAGGTCACATCT[A/G]TTCTTCAGCAAAGGT | 115677 |
rs756619913 | snp | C/G | | | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862049 | TTGAATTTGGAAAAG[C/G]GTAAGAATCATTCTC | 115677 |
rs756629447 | in-del | -/A | 0.0017355 | 0.0294064 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851420 | GTGAGTATGAAATGG[-/A]AAAAAAAAGTTACAT | 115677 |
rs756639069 | in-del | -/ACTATACTCATTATATATACTG | 1.65723e-05 | 0.00287852 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828151 | CCCACTTTTTTTTGC[-/ACTATACTCATTATATATACTG]CTTTAGTTGTGTTAG | 115677 |
rs756749916 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834755 | CAATGATGCCCACAT[G/T]TTTTTAAAGGAAACT | 115677 |
rs756759916 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847780 | CACCTATTTTATATA[A/G]AAAGAACAAGATAAT | 115677 |
rs756766126 | snp | A/G | 1.65701e-05 | 0.00287833 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851193 | CCACAGTGAGTAGAG[A/G]TGATCTCTCCATTTC | 115677 |
rs756769024 | in-del | -/ACAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807261 | TGAACACACACACAC[-/ACAT]ACATACATACACACA | 115677 |
rs756782007 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790240 | ATACTAGTAATAAAT[A/T]ATAATGCATTGAATA | 115677 |
rs756797937 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789591 | ACAGAGATCCAAACC[A/G]TATCAGCTGGAGTGT | 115677 |
rs756801182 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833513 | CCTGAACAGGCTAAA[C/T]CCAACTTAAACCAAA | 115677 |
rs756836616 | snp | A/G | 1.66827e-05 | 0.00288809 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824596 | GAGCCACTGTGCCCA[A/G]CCCAGTACATCCTAT | 115677 |
rs756940502 | in-del | -/GATA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847204 | AAATTTGAATAATTT[-/GATA]GATAACTAGAAGATA | 115677 |
rs756940886 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858412 | TTTCTAGGATGAGGA[A/C]ACTTTTATTTACATT | 115677 |
rs756978842 | snp | C/T | 1.66599e-05 | 0.00288611 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831465 | TTCCTTTTTCCTTTT[C/T]CAATAGCTTGACAAT | 115677 |
rs757052530 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798024 | ATAACCTACACACAT[C/T]CTCCCATGTACTTTA | 115677 |
rs757118471 | snp | A/C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842458 | GACTCTTATCCTGGA[A/C/G]GTTTGATTCCAAAGC | 115677 |
rs757154280 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864338 | GTTGCCCAGGCTAGA[A/G]TGCAGTGGCATGATC | 115677 |
rs757170668 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822823 | TGTGCTGCAAAGAAA[A/G]TAATAGAAATTCATT | 115677 |
rs757173135 | snp | C/G/T | 4.97767e-05 | 0.00498862 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828477 | TTATCAAGTCCTAAA[C/G/T]GTACAAGAGAAGAAG | 115677 |
rs757176411 | snp | A/G | 9.97821e-05 | 0.00706266 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865003 | ACTACCTTCACACTC[A/G]GTAATCAACAATACA | 115677 |
rs757182084 | snp | C/T | 3.32458e-05 | 0.00407698 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859672 | GTTGTAATTTCTTGA[C/T]TGGGCCTGCTGGGTG | 115677 |
rs757328072 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852095 | GCCCAAGAAATTATA[A/G]TCTCTTGTAAGCTAA | 115677 |
rs757339062 | snp | C/T | 1.6661e-05 | 0.00288621 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168842996 | TTTTACATTAGCTCC[C/T]CAATAAACTGACAAA | 115677 |
rs757378391 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829478 | GGTGCCTGCCACCAC[A/G]CCTGGCTAATTTTTG | 115677 |
rs757379188 | snp | C/T | 0.000182604 | 0.00955347 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851245 | GCAGAAACCTTTCTT[C/T]GACAACCTTATTCTG | 115677 |
rs757384448 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862264 | CATTGTTGCAGGCCT[A/G]TTGTCCAATTTAATA | 115677 |
rs757389670 | snp | C/T | 3.31263e-05 | 0.00406965 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862000 | CAGACTTTGCAAGGC[C/T]TTGTATTCTTTTCAA | 115677 |
rs757431028 | snp | C/T | 1.95337e-05 | 0.00312514 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802684 | GTCCGGTGAGTAGCT[C/T]AGTGTGGTTTGTGTG | 115677 |
rs757434671 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819214 | CCGAGATAAAGCACC[C/T]CCCTTTGAGAGATGA | 115677 |
rs757458217 | in-del | -/AAAA | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800921 | TTTTAAAAAAAAAAC[-/AAAA]AAAAAAAGAGATGGG | 115677 |
rs757487976 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831727 | CATGGCTCTAACTAT[G/T]ATTATTTAGCACTTA | 115677 |
rs757511120 | snp | A/C/G | 5.01897e-05 | 0.00500927 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856662 | GAGACAGTGTGAAAG[A/C/G]TGACTGAGAACATGA | 115677 |
rs757531792 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815541 | TGCTGCTCTGGACAT[G/T]AAAAAGAAAAGAATA | 115677 |
rs757580816 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796491 | TTTACGGTCATCTTG[A/C]TGTGAATATAGCAAA | 115677 |
rs757652552 | snp | A/T | | | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786519 | CAAGTGAGCATGCGT[A/T]TAACTCCCGTAAACA | 115677 |
rs757653084 | in-del | -/GAGACATTG | 1.66955e-05 | 0.0028892 | cds-indel, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855427 | TATTGAGACTGCAGA[-/GAGACATTG]GAGACATTGAAAAAG | 115677 |
rs757656049 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864352 | AGTGCAGTGGCATGA[-/T]CTCAGCTCACTGCAA | 115677 |
rs757677595 | snp | C/G/T | 3.31352e-05 | 0.00407022 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856755 | GCAAAGAGCCAGAAA[C/G/T]ACACAGCAGCGTTAA | 115677 |
rs757724813 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824137 | GATCCTCTTGGATAC[C/T]CTTCAGGATTATGCT | 115677 |
rs757776747 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847144 | AGAGACTAATGGCAC[A/G]GGAAACTGTTCACAT | 115677 |
rs757832201 | in-del | -/A | 6.62641e-05 | 0.00575566 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864895 | GGATCTTTGAATGGG[-/A]AAAAAAGGCCATTTT | 115677 |
rs757849484 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795765 | GTGCAATTTTTACAA[C/G]CACAAAGTAATTAGT | 115677 |
rs757876477 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814382 | TCAGAAATTCCTCCT[C/G]TAGATATACATTGGA | 115677 |
rs757905504 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849457 | ACCTCCCAGGTCCAA[C/G]CGATTCTCCTGCCTC | 115677 |
rs757942271 | snp | C/T | 1.66101e-05 | 0.0028818 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851296 | CCACACGCAGATTCA[C/T]TGTGCCATCAGCAAG | 115677 |
rs757955571 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822181 | TGCGATGAGATATTT[A/G]TTGACTGGCTTCATT | 115677 |
rs757976518 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835846 | CAGGCAAAATGAACA[C/T]GAATAATATTGGGGT | 115677 |
rs758034520 | snp | C/T | 3.31307e-05 | 0.00406992 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828226 | ACCTGCATCAGTGAG[C/T]TCTCCCACCCTGGCC | 115677 |
rs758141391 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804876 | TATAGTGTCTGTGAC[G/T]TTGTAACCAATAAAA | 115677 |
rs758144295 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800682 | TATGGAAACTGGCAA[C/G]GGAGGCCAATTTCCT | 115677 |
rs758191822 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790536 | CAAAGATACGAAACC[C/T]GAATCTGATCATGAG | 115677 |
rs758194371 | snp | G/T | 8.30668e-05 | 0.00644411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860941 | AATCATTTTGGCCTG[G/T]GTCCTACTGGCAGGG | 115677 |
rs758197408 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799734 | GTTCAAAACGTGTCA[C/T]CCCAGGCTGGATTGG | 115677 |
rs758222774 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842757 | TTAAGGGTCTCAATC[G/T]CCTCATGTGTAAAAT | 115677 |
rs758252923 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830782 | TAAAACTGGCAGTTA[A/G]GACTGTTACCAGTTT | 115677 |
rs758276188 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854879 | CATTCTGGAAAGAGC[A/G]TATGTGTTTTAGCTC | 115677 |
rs758319579 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820997 | TGTTCTGGAGCCAAC[A/G]GACAAGAAAACGGGA | 115677 |
rs758343736 | snp | C/T | 1.66521e-05 | 0.00288544 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831561 | CAAATACCATTTGTG[C/T]AAACTCAGTTTTTAG | 115677 |
rs758345758 | snp | A/G | 8.27797e-05 | 0.00643296 | synonymous-codon, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811593 | ATACAAGAACCTAAA[A/G]GAGTTTTCTCAAAAT | 115677 |
rs758363661 | snp | C/T | 1.66103e-05 | 0.00288182 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864807 | TTCACATCACAGAGA[C/T]CCATTTGTCTAACTG | 115677 |
rs758390210 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812381 | AGACCAAAGATGCCA[C/T]GGATTGGTTGCATCC | 115677 |
rs758396678 | in-del | -/G | 1.7648e-05 | 0.00297047 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851041 | TGACTTCCATTTTGC[-/G]ATAACAACTGGCTGA | 115677 |
rs758401522 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854480 | ATTCTTTTTTATTCA[A/G]TCCTTGAAATAATGC | 115677 |
rs758512368 | snp | C/G | 1.84626e-05 | 0.00303825 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855321 | CTCTTACTTCTTCCC[C/G]CTTGTTAGACATCCT | 115677 |
rs758535700 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829556 | CAACTCCTGACCTCA[A/G]GTGATCCGCCCATCT | 115677 |
rs758557330 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863183 | CTTTAAATGAAACAC[C/G]ACGTTGGAGCCTTAG | 115677 |
rs758605419 | in-del | -/TT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822106 | TGTTAACCAGCACTC[-/TT]TTTCTCTCCTCTCCA | 115677 |
rs758637043 | snp | C/T | 1.96988e-05 | 0.00313831 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802701 | GTGTGGTTTGTGTGC[C/T]TGCGTGTGAGGAGGG | 115677 |
rs758648239 | snp | A/G | 3.63379e-05 | 0.00426235 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834359 | CTGGGCGCATGTGCC[A/G]TAGAGAGGGATGGAC | 115677 |
rs758722037 | snp | C/T | 1.65773e-05 | 0.00287895 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859503 | CATGGCCAAATGATG[C/T]ATCCACAGAACAATT | 115677 |
rs758730682 | in-del | -/ACTC | 1.65954e-05 | 0.00288053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864976 | AAGGCATAAAACAAG[-/ACTC]ACTCTGAACATACTA | 115677 |
rs758808252 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803420 | GAAAAGCTAAGATTG[A/G]TGACATCATAAGCAG | 115677 |
rs758828414 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847884 | AAACATAGATCATTT[C/T]AATGATTTCCCTGAA | 115677 |
rs758832682 | snp | A/G/T | | | intron-variant, splice-donor-variant | NOSTRIN | GRCh38.p7 | 2:168826965 | GAATCTCCTGTAATT[A/G/T]TAAGTATATAGCAGG | 115677 |
rs758843975 | snp | G/T | 1.66092e-05 | 0.00288172 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843018 | ACTGACAAAATCAAC[G/T]GAAAAGTTGGAAAAG | 115677 |
rs758980756 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795396 | GCATTTGTAAAATGT[C/T]CTTGTTCTCATGCTT | 115677 |
rs759036307 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829563 | TGACCTCAGGTGATC[C/G]GCCCATCTTGGCCTC | 115677 |
rs759054475 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851862 | CCAGGTGTCTCTGAA[C/T]CCCTCCCAAGGCTGC | 115677 |
rs759088552 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840928 | ATTTGTAATTTTTAC[-/A]AGCATTTCAGGTCAT | 115677 |
rs759099624 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839625 | AAGTAAGAATACAGG[A/C]GTCTACAGCCGGGCG | 115677 |
rs759125770 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841130 | TACTTGGGAGGCTGA[A/G]ATGGGAGCATTGCTT | 115677 |
rs759151008 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838924 | AAGTAGCTGGGATTA[C/T]AGGCACTCACCACCA | 115677 |
rs759199861 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803116 | TTGGAGTCAAGGATC[A/G]CAAGTCCTGCAGGAG | 115677 |
rs759217666 | snp | A/C | 1.7396e-05 | 0.00294919 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851428 | GAAATGGAAAAAAAA[A/C]GTTACATTAATGGAG | 115677 |
rs759226481 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833256 | AAAGGACCAAATATT[C/T]ATGCGTCACACTCTC | 115677 |
rs759229295 | in-del | -/ACTT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862603 | CTTAGTGCTGGTCTC[-/ACTT]ACTTCTCAGAAAAGC | 115677 |
rs759245491 | in-del | -/AAGA | 1.65992e-05 | 0.00288085 | splice-donor-variant | NOSTRIN | GRCh38.p7 | 2:168862051 | AATTTGGAAAAGGGT[-/AAGA]AAGAATCATTCTCAA | 115677 |
rs759250084 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807087 | TTGGGTCTTAACTGT[A/G]AATAAGGGAATTAGA | 115677 |
rs759279446 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846497 | AATATTGTAAAGCCT[C/T]AAATGTGACTATAAG | 115677 |
rs759406033 | snp | G/T | 3.42097e-05 | 0.00413566 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811546 | GTTCATTGTTTTTTT[G/T]TTATTGTTCTTGTTT | 115677 |
rs759411961 | snp | A/G | 1.66363e-05 | 0.00288407 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864783 | TTATCAATCGGGCTG[A/G]GGCATGTGTTCACAT | 115677 |
rs759421348 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826059 | AAAATTTATCTTACC[G/T]CTCAAGATCTCTTTA | 115677 |
rs759485863 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813112 | GAGGGAATTTCTTCT[A/G]TAAGAAAATATTGTT | 115677 |
rs759522677 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843584 | AGTAGACACATAAAG[A/C]AGGAATTGTGGCAAA | 115677 |
rs759538371 | snp | A/G | 1.68069e-05 | 0.00289882 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842977 | TAAATGTGTGACATT[A/G]ATGTTTTACATTAGC | 115677 |
rs759540087 | snp | A/G | 1.65644e-05 | 0.00287783 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859559 | CTCCTACAAACTGTC[A/G]TCAATGTTAGCAGAA | 115677 |
rs759549332 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823509 | TGGCATTCTTTGGCT[C/T]GTAGATGCACCACTC | 115677 |
rs759565505 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803657 | CTCATAAATGACTAG[C/T]AATTTTAATAATGAC | 115677 |
rs759605927 | snp | C/T | 8.29304e-05 | 0.00643882 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168824708 | AAGCATTACAGAACA[C/T]GAGAAAAAGGTAAGT | 115677 |
rs759617707 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826491 | TCCTTCTCTTTCCAT[G/T]TTTACCCTGTCTTTT | 115677 |
rs759627330 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813548 | TTCTTGAAGTCTCTT[C/T]CTAGGGCTGCCATCT | 115677 |
rs759638259 | snp | A/C | 1.65831e-05 | 0.00287945 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864962 | GGCAACACAGCTACA[A/C]AGGCATAAAACAAGA | 115677 |
rs759641941 | snp | G/T | 1.65743e-05 | 0.00287869 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828145 | TTTGTTCCCCACTTT[G/T]TTTTGCCTTTAGTTG | 115677 |
rs759663629 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811973 | TGTACTTTTCACACC[C/G]ACAGCAATTATTTAC | 115677 |
rs759720280 | in-del | -/T | 0.000520249 | 0.01612 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824754 | AGGCAAAATCAACCC[-/T]TTTTTTATTTGTTTT | 115677 |
rs759752542 | snp | C/T | 1.65638e-05 | 0.00287778 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851164 | ACATATTTCTCTTTT[C/T]GGCCAAACCCTGACC | 115677 |
rs759784306 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854629 | TCATGCAACAGGTGT[C/G]TTTATTGTTCCTGAC | 115677 |
rs759864780 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818857 | TTTTTTTAATTTTTA[A/G]TTTTTGTGGGTATAT | 115677 |
rs759871336 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822983 | GATCAGTAGGACAGT[G/T]TTCTGTTCCTTACTA | 115677 |
rs759897152 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830371 | CTCTCACAAAATATA[A/G]AAGATTAGATTTTAT | 115677 |
rs759946594 | snp | A/G | 0.000115987 | 0.00761447 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860880 | AGGCATCTTCTGGTG[A/G]GCAGAGCAATCCAGG | 115677 |
rs759969300 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831353 | CTCCACCTCCAAATA[C/G]CATCACATTGAGGGA | 115677 |
rs760045899 | snp | A/G | 1.66065e-05 | 0.00288149 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831534 | GAATCAGCAAATTAA[A/G]GCAAGTATCCACAAA | 115677 |
rs760053391 | snp | A/G | 1.65974e-05 | 0.0028807 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831515 | ATCTTGTCATTAGCA[A/G]CTGGAATCAGCAAAT | 115677 |
rs760104803 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787149 | GCAGAAAGCTAGGAA[G/T]AATGAATAGTATTTG | 115677 |
rs760145301 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834871 | TACTTTATGTATTAT[C/G]TTAATATGTTATGAA | 115677 |
rs760229297 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859410 | TGAGTTAAATGCGTA[C/T]TTTTCTAACCTTTGT | 115677 |
rs760229804 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827927 | ATATGAAATAGGAAA[A/T]GAAAATCTAAATGAA | 115677 |
rs760239753 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816293 | TCACTCTGTAGCCAT[A/G]ACCCTGTTTAAGACG | 115677 |
rs760254100 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823154 | CCTGAATAGCTGGGA[C/T]TACAGGCGTGAGCCA | 115677 |
rs760255428 | in-del | -/AGG | 4.97038e-05 | 0.00498492 | cds-indel, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864865 | ACACGAGAAAAAAGA[-/AGG]AGGATGGTGGTTTGG | 115677 |
rs760261891 | snp | A/G | 1.66324e-05 | 0.00288374 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834266 | ACCAAGAAACATGAA[A/G]CACTTTTCCAGCTTG | 115677 |
rs760287071 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809523 | AGTATTATAGAAGAA[A/C]ACAAAAGGCTTAGGG | 115677 |
rs760308065 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797233 | TAGCTGGGACTACAG[A/G]TACGTACCACCATGC | 115677 |
rs760314391 | snp | A/C/G | 3.51935e-05 | 0.00419473 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855493 | TGAATGGCCAGAAAA[A/C/G]GGACCATATGATGCT | 115677 |
rs760350502 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791091 | TGGTGTGCTGCACCC[A/G]TTAACTCATCATTTA | 115677 |
rs760362545 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844047 | AAACTATATTTAAAC[A/G]TGAATTAACCTCGAA | 115677 |
rs760424889 | snp | A/C | 3.31378e-05 | 0.00407036 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864861 | TTATACACGAGAAAA[A/C]AGAAGGAGGATGGTG | 115677 |
rs760475607 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832087 | GTGAGGGGTGGGTAG[C/T]GATATGTAAAAGGGG | 115677 |
rs760491214 | snp | G/T | 2.26324e-05 | 0.00336388 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811670 | ACAAAATGCACGTTT[G/T]CAATAAATGGTTCTT | 115677 |
rs760492618 | in-del | -/ATAAGGATAT | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863884 | AGTGAGCCAGGCAGC[-/ATAAGGATAT]ATGATCCAACGTGAT | 115677 |
rs760508695 | snp | C/T | 1.66799e-05 | 0.00288785 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855415 | CTAAAACCAAAATTA[C/T]TGAGACTGCAGAGAG | 115677 |
rs760514633 | snp | C/T | 3.31373e-05 | 0.00407032 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864919 | CCATTTTCCTGCCGC[C/T]TATGTGGAGGAGTTA | 115677 |
rs760522030 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841201 | GATTCTGTCACTGAA[A/C]TCCAGCCTGGGTGAC | 115677 |
rs760549328 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847453 | ATAAAGAGGGGTCTA[A/G]ATATTCTAAAGTTTG | 115677 |
rs760638982 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852721 | TTAGATCAGGCACTG[A/C]AGTAAACCCTGATTG | 115677 |
rs760656772 | snp | C/G | 5.73049e-05 | 0.00535249 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850974 | GACATAGTCAAGAGG[C/G]TAATCATGAGACTTT | 115677 |
rs760730850 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803215 | CATGTTTGTTCGTTT[G/T]GGTAATGTTTGGAGC | 115677 |
rs760759953 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814387 | AATTCCTCCTCTAGA[C/T]ATACATTGGATAGAA | 115677 |
rs760851816 | snp | A/C | 1.65652e-05 | 0.0028779 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828200 | CTCAGAGGGAATGAA[A/C]TCCACAGCGGACCTG | 115677 |
rs760869354 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790529 | TTCCTGCCAAAGATA[-/C]GAAACCTGAATCTGA | 115677 |
rs760879165 | snp | C/T | 1.65696e-05 | 0.00287828 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861950 | CTAATTACAGCTTTA[C/T]CTATTTCAGCCCCTG | 115677 |
rs760881804 | snp | C/G | 1.67405e-05 | 0.00289309 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856822 | ATGTAGTGATGAAAA[C/G]GGTTATTTTTAGAAT | 115677 |
rs760936455 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853049 | ATTCTTGAAAATTTG[A/T]CTAGGGTTCTACCAA | 115677 |
rs760968849 | snp | A/G | 3.32105e-05 | 0.00407482 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851270 | ATTCTGTTCCCCTTG[A/G]CATTGCAGTGCCACA | 115677 |
rs761030156 | snp | A/G | 1.65699e-05 | 0.00287831 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851189 | CTGACCACAGTGAGT[A/G]GAGATGATCTCTCCA | 115677 |
rs761031757 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807242 | AGGTAAGTTCCAAGA[C/T]TTTCTGAACACACAC | 115677 |
rs761050068 | snp | A/G | 8.31594e-05 | 0.0064477 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824729 | AAAGGTAAGTATTGT[A/G]GCAGAGGTAAGGCAA | 115677 |
rs761070863 | snp | C/T | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863762 | GGTGAGACATACTTA[C/T]AGCAGCCAACACGCC | 115677 |
rs761113983 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819842 | CCAGCCCAGAGGGCT[A/G]GCTCGGTGACATTTG | 115677 |
rs761123987 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862944 | ACAGGGACACCACAC[A/G]TTTGCTATTTATTGG | 115677 |
rs761144969 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851917 | AGACATCTCCAGGCT[C/G]TTCCTCCAGAAGACT | 115677 |
rs761177643 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817070 | CACTGTGTTAAGTGT[-/G]TCTTATACTTGATCT | 115677 |
rs761228389 | snp | C/T | 3.31851e-05 | 0.00407326 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860919 | CTCCAGGTAATCCCA[C/T]GCCCACAATCATTTT | 115677 |
rs761285139 | in-del | -/GA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847514 | TTTTATCAGTTCTAT[-/GA]GAGTCATTTAAATGA | 115677 |
rs761309524 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837300 | CACTTTTTTAACATC[-/T]TTTTTTTTTTTTTTT | 115677 |
rs761366396 | snp | A/G | 1.66023e-05 | 0.00288113 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860930 | CCCATGCCCACAATC[A/G]TTTTGGCCTGGGTCC | 115677 |
rs761369726 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848690 | TAGCCAGATGCAAAA[G/T]AACAAGTAGTGTATG | 115677 |
rs761396233 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829849 | GCAGTGGTTAAGGGG[G/T]AGTTTCAAGGGAATA | 115677 |
rs761399505 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798102 | TAAATAGTCATAAAT[-/A]ACTTATTTGTATTTT | 115677 |
rs761423516 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798691 | TGAGTGCGGGTCAGA[A/T]ATGTAGGACCAGAGA | 115677 |
rs761444745 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860551 | TGGTGGGCACCTGTA[A/C]TCCCAGCTACGGGGG | 115677 |
rs761452344 | snp | A/C | 1.67784e-05 | 0.00289636 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834298 | AGAAAGCTCCAAGCA[A/C]TCTATGACTGAGAAG | 115677 |
rs761457159 | snp | C/G | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861962 | TTATCTATTTCAGCC[C/G]CTGGTGCAGCCCAGC | 115677 |
rs761504130 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784850 | CTCAATTTTTCAAGT[C/T]CACTGTATCAGTCTA | 115677 |
rs761505481 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823375 | GAGTGGCTTAAACAA[-/T]CAGAAGTGTGTTGTC | 115677 |
rs761563256 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823601 | TTTTCTCTTTATATG[A/G]GACACATCCACTATA | 115677 |
rs761586678 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850188 | AACGTGCTGGGATTA[C/T]AGGCATGAGCCACTG | 115677 |
rs761586813 | snp | A/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864107 | CAAATAGCTGGGACT[A/T]CAGGCGTGTGCCACC | 115677 |
rs761612290 | in-del | -/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863910 | TGATCCAACGTGATC[-/T]TTTTTTATTTTTTTT | 115677 |
rs761618255 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823067 | TGTCGCCCAGGCTAG[C/T]GTGCAGTGGCGCAAT | 115677 |
rs761628998 | snp | A/T | 1.66757e-05 | 0.00288749 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865020 | TAATCAACAATACAG[A/T]GTGGTTCAAATAAGA | 115677 |
rs761717143 | snp | C/T | 1.65745e-05 | 0.00287871 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856702 | CAGGCCTGGAACGAA[C/T]GCTTAAAACGTACTC | 115677 |
rs761717633 | in-del | -/T | 1.70023e-05 | 0.00291563 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842945 | GGAATTACAAAGGGC[-/T]TTCAAAAATGTGTTA | 115677 |
rs761832585 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793701 | TGTGACTCTATTTAC[C/G]TTTTGGTTAAAGTTA | 115677 |
rs761850181 | in-del | -/TTTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863228 | AATTTGAAATCATTA[-/TTTG]TTTGTTTGAATTCTT | 115677 |
rs761884817 | snp | A/G | 3.31257e-05 | 0.00406962 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859571 | GTCATCAATGTTAGC[A/G]GAACTTGAGCAAAGA | 115677 |
rs761926170 | snp | C/T | 1.66045e-05 | 0.00288132 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859465 | CCTATCCAGTTGTGC[C/T]TCATTTACTAGAAAT | 115677 |
rs761952243 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806055 | TCTATGACAGTCTGC[C/T]ACAGGGATTCCAAAT | 115677 |
rs762083099 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789189 | ATGGGAAAATGTTAT[A/G]AGGACATAGAACCAA | 115677 |
rs762139969 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841838 | AAATATACAGGGGAA[C/G]TTGTCTATGTTTATG | 115677 |
rs762181044 | in-del | -/AAAAAAAAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841238 | AGACCCTGTCTCCAA[-/AAAAAAAAAAAA]AAAAAAAAAAAAGAA | 115677 |
rs762193469 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854227 | AAATAAAATATTTTT[A/G]TCTGTATATGTTTTT | 115677 |
rs762203605 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792585 | CTCCTGAGTAGCTGG[G/T]ACTACAGGTGCTTAA | 115677 |
rs762245308 | snp | C/G | | | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851140 | CAATAACTTAAACCA[C/G]TACAGCCAACATATT | 115677 |
rs762256128 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809933 | GTTTTGTTTACACTG[C/T]AGAGAGGTTTTTAAT | 115677 |
rs762297924 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808415 | CACTCTAAATCCCTC[A/G]AATCCATCTCTCTGC | 115677 |
rs762328528 | snp | A/G | 1.68032e-05 | 0.0028985 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862086 | TTTAATTGCCTTCCC[A/G]TATTGAGATTCTTAG | 115677 |
rs762358991 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807738 | GAGCGAGGTACGAGG[-/C]AAAGCCATGGGCCAG | 115677 |
rs762371456 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805839 | GGTCCGTAGCTCCTA[C/G]GAGAATCTGACTCGC | 115677 |
rs762396593 | snp | A/T | 1.65992e-05 | 0.00288085 | splice-donor-variant | NOSTRIN | GRCh38.p7 | 2:168862051 | GAATTTGGAAAAGGG[A/T]AAGAATCATTCTCAA | 115677 |
rs762460999 | in-del | -/AAAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860686 | AAAAAAAAAAAGAAA[-/AAAC]AAACAGAAAAAACAA | 115677 |
rs762499387 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837791 | AGTCTTACCTTAGTT[A/T]ACTTCTCGGAAGTAT | 115677 |
rs762545552 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802169 | GCCAGTTGTTTGCTC[C/T]CTCTAGGAATTAGCT | 115677 |
rs762557779 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786952 | CAGGCTGGTCTCGAA[A/T]GCCTGACCTCAAGTG | 115677 |
rs762565095 | snp | A/C | 1.93951e-05 | 0.00311403 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802664 | GAGGGACCCACTGAC[A/C]GATTGTCCGGTGAGT | 115677 |
rs762591970 | snp | C/T | 1.7093e-05 | 0.00292339 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834320 | ACTGAGAAGGAGAAG[C/T]GGAAGGTAAGCTGTC | 115677 |
rs762602565 | snp | G/T | 1.69841e-05 | 0.00291407 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851403 | TGTTAACGGATTACT[G/T]TGTGAGTATGAAATG | 115677 |
rs762635208 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861652 | GAATGGCAAAACTGG[C/T]GAATGTTTTCCAAAA | 115677 |
rs762639030 | snp | C/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845077 | ACTTGGGTCAAAGAG[C/G]GGAACAAATGAGAAA | 115677 |
rs762681375 | snp | A/C | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861972 | CAGCCCCTGGTGCAG[A/C]CCAGCTCAGCAGCAG | 115677 |
rs762832904 | snp | G/T | 1.6949e-05 | 0.00291105 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842954 | AAGGGCTTTCAAAAA[G/T]GTGTTAGTAAATGTG | 115677 |
rs762841454 | in-del | -/AGTTCTATATAA | 1.67713e-05 | 0.00289575 | cds-indel, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843114 | CTAGAGAACTGCTAC[-/AGTTCTATATAA]CAGGTAAGTTATATA | 115677 |
rs762857614 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798646 | GACAGTAAATCTAAC[C/T]GGAAGCCAGGCTGGA | 115677 |
rs762891827 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848473 | ATACAAAAGCTAAAG[C/T]TGCATGTGATTGGCA | 115677 |
rs762913254 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822696 | TTTTAGCTATAGATG[A/G]GTCTGTAAATAGGAC | 115677 |
rs762968427 | snp | A/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851126 | ATTCAACTTTTATGC[A/G]ATAACTTAAACCAGT | 115677 |
rs763011157 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823699 | TGAGGTCACATTCAC[A/G]GGCACTGGGGAGTAG | 115677 |
rs763021614 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795249 | GACTAAAACGACTCT[A/G]TACTAGACATTCTAG | 115677 |
rs763023201 | snp | G/T | 2.22725e-05 | 0.00333702 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851020 | AGGTGTGTCAGTGTT[G/T]GATGAGTGACTTCCA | 115677 |
rs763069222 | in-del | -/CAAA | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863776 | TAGCAGCCAACACGC[-/CAAA]CAAACAATCAAAAAC | 115677 |
rs763075185 | snp | A/G | 1.77219e-05 | 0.00297668 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843165 | TGTGGAGCTTTGTGT[A/G]ACCTTGAAGATGGAG | 115677 |
rs763099144 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810199 | GAAATTAGCAATTTC[C/T]TCATTAAAGCTTTGC | 115677 |
rs763111687 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813115 | GGAATTTCTTCTGTA[A/G]GAAAATATTGTTATC | 115677 |
rs763118925 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821363 | TTCTCAAAAGTGGTG[A/G]GGTGAGAACAAACCT | 115677 |
rs763149916 | snp | A/G | 1.66363e-05 | 0.00288407 | splice-acceptor-variant | NOSTRIN | GRCh38.p7 | 2:168860793 | TTATGTCATTTGAAC[A/G]GGAGCATACTCATAG | 115677 |
rs763150815 | in-del | -/T | 3.63749e-05 | 0.00426452 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811539 | TCTTCCTGTTCATTG[-/T]TTTTTTGTTATTGTT | 115677 |
rs763171932 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834140 | TTAAAGCTAGCACAT[A/G]AATGTGCTTTGTTCC | 115677 |
rs763188252 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864053 | GCTCACTGCAACCTC[C/T]GTCTCCTGGATTCAA | 115677 |
rs763198825 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789974 | ATGCTTTCTTAATGC[C/T]GCTGGTTTTTAGTCA | 115677 |
rs763199972 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855750 | GTTTCTGAAATTGGC[A/T]AGAATGAGAGATAAT | 115677 |
rs763219001 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834593 | ATAGAAGGGATCTCA[C/T]TGTGCTGCCCAGGCT | 115677 |
rs763259292 | in-del | -/CAGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788931 | AGATAGATAGATAGA[-/CAGA]TAGATGATAGATATT | 115677 |
rs763269549 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830086 | AGGAATTGCTAGCAA[A/G]CAATATAACCTTCTG | 115677 |
rs763276451 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804376 | GTCATGGGGAGGGCG[G/T]ATATCCCTTCAGCCT | 115677 |
rs763382841 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832788 | AGGAATTGTTTTGTA[-/T]TTTTTTTTAAAGAAA | 115677 |
rs763420039 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799097 | TTGTGTTATTTTCAT[A/G]GAAATTCTTGGCAAA | 115677 |
rs763448025 | snp | A/C/G | 3.31268e-05 | 0.00406968 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859563 | TACAAACTGTCATCA[A/C/G]TGTTAGCAGAACTTG | 115677 |
rs763449464 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855308 | CAGGGAATAGCAACT[C/G]TTACTTCTTCCCCCT | 115677 |
rs763454012 | in-del | -/A | 0.000121721 | 0.00780037 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864868 | CGAGAAAAAAGAAGG[-/A]GGATGGTGGTTTGGA | 115677 |
rs763456300 | in-del | -/CTCCCCA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793234 | GTTCCTGGCAACAGC[-/CTCCCCA]CTCTTCCTAATCCTT | 115677 |
rs763549273 | snp | A/G | 1.6588e-05 | 0.00287988 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828433 | AGAAAACTTGGCAAA[A/G]CAATTGAATTGGAAG | 115677 |
rs763552979 | snp | C/T | 1.6717e-05 | 0.00289106 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855374 | ATCCTAACAGTGCAA[C/T]GGATAAAGAGAGACG | 115677 |
rs763605323 | snp | C/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856023 | CAATGGAATACTAGA[C/G]AGCAAATTCAAGATA | 115677 |
rs763618110 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811618 | CAAAATGGAGAGAAT[A/T]TCTGCAAACAGGTCA | 115677 |
rs763625808 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784727 | TCCTCCTGTAGTTTT[C/T]ATCTCTATCTTCCCT | 115677 |
rs763651810 | snp | A/G | 8.28851e-05 | 0.00643705 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860819 | CATAGCTATGTGAAA[A/G]TATCTCGGCCTTTTT | 115677 |
rs763852206 | snp | C/G | 1.67466e-05 | 0.00289362 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831453 | GCAAAGCTTTGTTTC[C/G]TTTTTCCTTTTTCAA | 115677 |
rs763872718 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790123 | CATCGCTCTTTGCCT[C/T]GTGTGTTGAACCATC | 115677 |
rs763947594 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842452 | GACCAGGACTCTTAT[A/C]CTGGAAGTTTGATTC | 115677 |
rs763956548 | snp | G/T | 1.66189e-05 | 0.00288256 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864798 | AGGCATGTGTTCACA[G/T]CACAGAGACCCATTT | 115677 |
rs763975552 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791109 | AACTCATCATTTAAC[A/G]TTAGGTATATCTCCT | 115677 |
rs764058109 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804567 | GAAATGGATTGCAAA[C/T]GAGTGCCTCATGAAA | 115677 |
rs764107544 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787377 | ATACTGCTTACACTG[C/T]CACAGAGACCTCTTT | 115677 |
rs764115930 | snp | A/G | 1.65693e-05 | 0.00287826 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864865 | ACACGAGAAAAAAGA[A/G]GGAGGATGGTGGTTT | 115677 |
rs764135471 | snp | C/G | 2.36231e-05 | 0.00343671 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811680 | CGTTTGCAATAAATG[C/G]TTCTTCCTCTTTAGT | 115677 |
rs764203732 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789049 | AATCCATCCTAAACC[C/G]ATTCTCCACTAAAGG | 115677 |
rs764235648 | snp | C/G | 1.77688e-05 | 0.00298062 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834347 | TGTCATGGCTGGCTG[C/G]GCGCATGTGCCATAG | 115677 |
rs764295592 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850334 | ACAAAATAAAGAGGC[-/T]TATGTGTCTACCTGC | 115677 |
rs764381153 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830750 | ATATTCACTTCAGGG[G/T]TAATGGAGACACACA | 115677 |
rs764492923 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795658 | TATAAGACAGTTTTG[C/T]ATGTATATAATAAGT | 115677 |
rs764496139 | snp | A/G | 1.66021e-05 | 0.0028811 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851272 | TCTGTTCCCCTTGGC[A/G]TTGCAGTGCCACACG | 115677 |
rs764505235 | snp | A/T | 1.65658e-05 | 0.00287795 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828201 | TCAGAGGGAATGAAA[A/T]CCACAGCGGACCTGC | 115677 |
rs764528657 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849045 | ATATAGAGGAATACC[A/G]TACTGAATCAGGCCA | 115677 |
rs764537179 | snp | C/G | 8.2848e-05 | 0.00643561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851190 | TGACCACAGTGAGTA[C/G]AGATGATCTCTCCAT | 115677 |
rs764551859 | snp | A/C | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786299 | ATTATTTCTCTAAAA[A/C]AATAATTAGTCACAG | 115677 |
rs764566541 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851943 | AGACTCACTTCCAAG[A/C]TGACTCACAGGGCTG | 115677 |
rs764652484 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841237 | CAGACCCTGTCTCCA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAGAA | 115677 |
rs764667471 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819115 | TCTGACTATTTTAAT[A/G]AGGGAATGAAAATTT | 115677 |
rs764718648 | snp | A/C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848786 | CCAGGGGATGCAGAG[A/C/T]GTAGGAAATGAGAAG | 115677 |
rs764754575 | in-del | -/AC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858024 | CAATGACCCGTGGCT[-/AC]AGTTTTTATGAAATT | 115677 |
rs764807896 | snp | C/T | 1.65701e-05 | 0.00287833 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851194 | CACAGTGAGTAGAGA[C/T]GATCTCTCCATTTCT | 115677 |
rs764836494 | snp | A/G | 3.31301e-05 | 0.00406989 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861966 | CTATTTCAGCCCCTG[A/G]TGCAGCCCAGCTCAG | 115677 |
rs764838224 | snp | A/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856136 | TGAAAGAATTTCAAA[A/G]TCTCATCTGGAAAAA | 115677 |
rs764892002 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804706 | GCTACTGTTCTTAAC[C/T]GGGCCCACACCAATG | 115677 |
rs764912679 | snp | C/T | 4.97121e-05 | 0.00498534 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856711 | AACGAATGCTTAAAA[C/T]GTACTCCAGCACCTC | 115677 |
rs764928814 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796277 | GGCCTTCGGAAGACA[C/T]GTTAAGGTGTGTCAA | 115677 |
rs764943962 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828076 | GTGGTGAATCAGATG[C/T]GATGCTGTATTTCTA | 115677 |
rs764988261 | snp | C/T | 1.66477e-05 | 0.00288506 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831559 | CACAAATACCATTTG[C/T]GTAAACTCAGTTTTT | 115677 |
rs765002530 | snp | G/T | 3.32132e-05 | 0.00407499 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860935 | GCCCACAATCATTTT[G/T]GCCTGGGTCCTACTG | 115677 |
rs765016791 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859682 | CTTGATTGGGCCTGC[C/T]GGGTGGAGTGGCTTA | 115677 |
rs765057360 | in-del | -/TT | | | intron-variant, frameshift-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850987 | GGCTAATCATGAGAC[-/TT]TGTTCAGTCTGTCTT | 115677 |
rs765076217 | snp | A/G | 1.69178e-05 | 0.00290837 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834308 | AAGCAATCTATGACT[A/G]AGAAGGAGAAGCGGA | 115677 |
rs765099219 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836388 | ACAGTGCTCTCTCCT[C/T]TCCTCCAGCTGGTAA | 115677 |
rs765119231 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823131 | AAGAGATTCTCCTGC[C/T]TCAGCCTCCTGAATA | 115677 |
rs765124040 | snp | A/G | 3.32751e-05 | 0.00407878 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865013 | CACTCGGTAATCAAC[A/G]ATACAGTGTGGTTCA | 115677 |
rs765154950 | snp | C/G | 1.65767e-05 | 0.00287891 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864947 | TTACCTTCAAATGCT[C/G]GCAACACAGCTACAA | 115677 |
rs765202216 | in-del | -/A | 1.69911e-05 | 0.00291466 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842948 | TTACAAAGGGCTTTC[-/A]AAAAATGTGTTAGTA | 115677 |
rs765214146 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844314 | CTCTACATAAATATG[A/G]CCAAATTAAATAACT | 115677 |
rs765231722 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852099 | AAGAAATTATAATCT[C/T]TTGTAAGCTAATCTC | 115677 |
rs765242985 | snp | C/T | 1.83337e-05 | 0.00302762 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855509 | GGACCATATGATGCT[C/T]AGAGGTTTCATTCAG | 115677 |
rs765260399 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863074 | ACCCATGGATGCAGC[A/G]TTTAAGTTACATCAT | 115677 |
rs765265334 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820697 | CCGGCAGAAACACTG[C/G]GGCACAGGAGAAAAG | 115677 |
rs765291833 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863996 | GCTCACTGCAACCTC[C/T]GTCTCCTGGATTCAA | 115677 |
rs765349195 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808542 | AAGGCCCCATGGCTT[C/T]TTGTTGAGTCTTTGT | 115677 |
rs765400693 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821155 | TTATCCTATTTAATG[C/T]TCTTTGTGCTGCTTC | 115677 |
rs765421343 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806116 | TCCCTTCAGAGAGGG[A/G]CAGTGCTTTGAAACA | 115677 |
rs765453560 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820038 | GAGCTGTGCTGATTC[A/G]GAACACTGCAATTAA | 115677 |
rs765477107 | snp | C/T | 0.000206164 | 0.0101508 | synonymous-codon, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811581 | GTATAATAAAGTATA[C/T]AAGAACCTAAAGGAG | 115677 |
rs765527089 | snp | A/G | 1.66335e-05 | 0.00288383 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843003 | TTAGCTCCTCAATAA[A/G]CTGACAAAATCAACT | 115677 |
rs765545817 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797387 | CAGGCATGAGCTGCC[A/G]CACCCAGCCTAAACT | 115677 |
rs765546290 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832467 | TTTTCATCTCCAAAG[C/T]GTTAGTGCCCACAGA | 115677 |
rs765576714 | snp | C/G | | | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826896 | CCTTCCCACCCAACT[C/G]CAAGCAACCACTGAC | 115677 |
rs765599299 | in-del | -/CAGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788927 | AGATAGATAGATAGA[-/CAGA]TAGATAGATGATAGA | 115677 |
rs765615683 | snp | A/T | 1.66283e-05 | 0.00288338 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828405 | GCTTATGTGTCTTTT[A/T]TGTTTTATTTCCAGA | 115677 |
rs765711805 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796521 | AAATTCTCTTAGATG[A/T]TCTTGGCAAACTTGT | 115677 |
rs765853212 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806844 | CTTCCACCTGACTGC[A/C]CTTCTTCTCAGCAAG | 115677 |
rs765858551 | in-del | -/TCTC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808515 | ATGCATCCAGGTCTT[-/TCTC]TCTTGCACAAGGCCC | 115677 |
rs765881323 | in-del | -/GTAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862547 | CTCAACTTAGTGTAA[-/GTAA]GTAAGTGCAAATTCT | 115677 |
rs765881952 | snp | C/G | 1.6563e-05 | 0.00287771 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861976 | CCCTGGTGCAGCCCA[C/G]CTCAGCAGCAGACTT | 115677 |
rs766044969 | snp | C/T | 1.6585e-05 | 0.00287962 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828442 | GGCAAAGCAATTGAA[C/T]TGGAAGCAATAAAAC | 115677 |
rs766067866 | snp | C/T | 1.69057e-05 | 0.00290733 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842966 | AAATGTGTTAGTAAA[C/T]GTGTGACATTGATGT | 115677 |
rs766096074 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850901 | AAAGTGTGTGAGTGA[C/T]TTAAGATACCAAGAC | 115677 |
rs766117643 | in-del | -/A | 0.000169537 | 0.00920543 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843126 | TACCAGGTAAGTTAT[-/A]ATATTCACATTTTTT | 115677 |
rs766155651 | snp | C/G | 7.77711e-05 | 0.00623534 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802671 | CCACTGACAGATTGT[C/G]CGGTGAGTAGCTCAG | 115677 |
rs766168624 | in-del | -/AACA | 0.000132659 | 0.00814321 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861923 | ATTCATTTGCCTGCT[-/AACA]AACACAGCATACTAA | 115677 |
rs766176868 | snp | C/T | 4.06298e-05 | 0.00450702 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802596 | ACCTTGATTACAGTG[C/T]CCAGAATGCTGGAGC | 115677 |
rs766214149 | snp | A/C | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800685 | GGAAACTGGCAAGGG[A/C]GGCCAATTTCCTCAG | 115677 |
rs766227276 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823804 | CCTTTGGGCTGGGCA[C/T]AGTGGCTCACGCCTG | 115677 |
rs766271431 | in-del | -/CT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829689 | GTTAAGCACTTTATA[-/CT]CTACTTCCAGGCAAC | 115677 |
rs766314242 | snp | A/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857053 | GGGCCTAGAAACCAT[A/G]TGCACTTTAACCCAG | 115677 |
rs766330470 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823976 | GCTACTTGAGAGGCT[A/G]AGGCAAAAGAATCAC | 115677 |
rs766364348 | snp | C/G | 1.65641e-05 | 0.00287781 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864870 | AGAAAAAAGAAGGAG[C/G]ATGGTGGTTTGGATC | 115677 |
rs766364452 | snp | G/T | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856739 | CTCCTCCTTCTCTGA[G/T]GCAAAGAGCCAGAAA | 115677 |
rs766431787 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840739 | TTTAACAGCCTTTGT[C/G]TCTGTCCTTGAAACT | 115677 |
rs766451592 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846635 | TAGAAATAACCTATA[C/T]TTTTCACAATAATAA | 115677 |
rs766473505 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821624 | AAGACATAAATAAAA[C/T]TGTAAGGGGAGAGTG | 115677 |
rs766487446 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853612 | GGGAAGCCTTGGACT[C/G]GTATGGGAGCTATGT | 115677 |
rs766526101 | snp | C/T | 1.7821e-05 | 0.00298499 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834197 | CAGCCTCTGCTCCTT[C/T]TTTTCTTGTTTGTAT | 115677 |
rs766531949 | snp | A/T | 1.66263e-05 | 0.00288321 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860796 | TGTCATTTGAACAGG[A/T]GCATACTCATAGCTA | 115677 |
rs766542322 | snp | C/T | 1.80788e-05 | 0.0030065 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851037 | ATGAGTGACTTCCAT[C/T]TTGCATAACAACTGG | 115677 |
rs766551545 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811678 | CACGTTTGCAATAAA[C/T]GGTTCTTCCTCTTTA | 115677 |
rs766583525 | snp | C/T | 4.97888e-05 | 0.00498918 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860806 | ACAGGAGCATACTCA[C/T]AGCTATGTGAAAATA | 115677 |
rs766651650 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808846 | TAAAAAGAAATGTAA[C/T]TAGACAAATGTTCAT | 115677 |
rs766659292 | snp | G/T | 1.93894e-05 | 0.00311357 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811610 | AGTTTTCTCAAAATG[G/T]AGAGAATTTCTGCAA | 115677 |
rs766678589 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784560 | GTGATTCCAAAACTT[-/A]ACACGTACTCATTCT | 115677 |
rs766727820 | snp | G/T | 1.65625e-05 | 0.00287766 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859589 | ACTTGAGCAAAGACC[G/T]CAACCCAGCCATCCT | 115677 |
rs766791099 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830277 | TAATGGATGTCATGA[A/G]CACCCCCGAAATGCT | 115677 |
rs766795932 | in-del | -/AAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853865 | TGTAATAAATAATAT[-/AAAAA]AAAGAAATATTTATT | 115677 |
rs766962193 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855881 | AAATTAAATTCTGTA[C/T]GTAGAAGTTAGGCAT | 115677 |
rs766966628 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819861 | CGGTGACATTTGCTG[A/T]CAGAGTCCCCATCCT | 115677 |
rs767000466 | snp | C/T | 1.68989e-05 | 0.00290674 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828546 | GTTTAAAGCAAGATT[C/T]CTGTGTTTAGCCCAG | 115677 |
rs767029193 | snp | A/G | 1.68732e-05 | 0.00290454 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831435 | CAACTAAACAAGAAG[A/G]AAGCAAAGCTTTGTT | 115677 |
rs767102256 | snp | G/T | 3.31433e-05 | 0.0040707 | stop-gained, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864854 | ATTGTGATTATACAC[G/T]AGAAAAAAGAAGGAG | 115677 |
rs767129603 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795440 | AAAGCCATAGATCAC[A/G]GCTATAGGATGACTT | 115677 |
rs767134914 | in-del | -/CTAA | 1.65993e-05 | 0.00288086 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864815 | CAGAGACCCATTTGT[-/CTAA]CTAACTGTATTTTCA | 115677 |
rs767164672 | snp | G/T | 9.49713e-05 | 0.00689033 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811553 | GTTTTTTTGTTATTG[G/T]TCTTGTTTTTCAGTA | 115677 |
rs767181789 | in-del | -/TG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848229 | AAGAAGCAAAACATT[-/TG]ATAGGCTATTCTGTG | 115677 |
rs767225819 | snp | C/T | 1.66751e-05 | 0.00288744 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855397 | GAGAGACGAAAGTCT[C/T]TACTAAAACCAAAAT | 115677 |
rs767267903 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841140 | GCTGAGATGGGAGCA[C/T]TGCTTGAACCCGGGA | 115677 |
rs767291870 | snp | A/T | 1.66239e-05 | 0.00288299 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864787 | CAATCGGGCTGAGGC[A/T]TGTGTTCACATCACA | 115677 |
rs767349295 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789286 | TAATGAAGACATACC[G/T]GAGACTGGGTAATGT | 115677 |
rs767369530 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847427 | GAATCAATCAGAGCC[C/T]CTGAATGATTATAAA | 115677 |
rs767427077 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828882 | AAAAGTCTAATTTAT[A/G]CAATCTCAACTTTAT | 115677 |
rs767427453 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862688 | TTACTTAACATGGAA[A/C]GGTATTACGTAGTGG | 115677 |
rs767429044 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800236 | TGAGTGAGGTCAGGG[A/G]ACACCTGAAGATCCA | 115677 |
rs767444754 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848674 | ATTATGCTAAGTGAA[A/C]TAGCCAGATGCAAAA | 115677 |
rs767460271 | in-del | -/CACGCG/CACGCGCACACC/CACGCGCG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834515 | GCGCGCGCACACACA[-/CACGCG/CACGCGCACACC/CACGCGCG]CACACACACACACAC | 115677 |
rs767541197 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799362 | CTACAAGATTCTTTG[A/C]TCCTCTTACTCACAT | 115677 |
rs767566434 | snp | A/G | 1.68781e-05 | 0.00290495 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843122 | ACTGCTACCAGGTAA[A/G]TTATATATTCACATT | 115677 |
rs767588283 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826363 | ATTTTTATCCATACC[A/G]AAATCTGTGTTAGGT | 115677 |
rs767612629 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842372 | GTATGTATTAATTAC[C/T]TATCCCCATCACAGA | 115677 |
rs767656679 | in-del | -/TTT | 2.5256e-05 | 0.0035535 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824765 | CCCTTTTTTTATTTG[-/TTT]TTTTTTGTTTGTTTG | 115677 |
rs767703840 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843610 | GCAAATTATCTGATA[A/C]TAATGGGCAAAATAT | 115677 |
rs767729458 | snp | A/G | 4.97616e-05 | 0.00498782 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168824709 | AGCATTACAGAACAC[A/G]AGAAAAAGGTAAGTA | 115677 |
rs767731516 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822985 | TCAGTAGGACAGTTT[C/T]CTGTTCCTTACTAGT | 115677 |
rs767791820 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810458 | CTAAGCACCACATAC[C/T]AAGTGCTTTGTTGAC | 115677 |
rs767793201 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786099 | CTATAGATATAAGAC[A/G]TTGGTATCATCGTTA | 115677 |
rs767888315 | snp | C/T | 0.000314833 | 0.0125426 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860887 | TTCTGGTGGGCAGAG[C/T]AATCCAGGTTCTTCA | 115677 |
rs767897252 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861807 | TGGTTATTGAATCAA[G/T]GAATGAACATTATAT | 115677 |
rs767898158 | snp | A/G | 3.31746e-05 | 0.00407262 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864967 | CACAGCTACAAAGGC[A/G]TAAAACAAGACTCTG | 115677 |
rs767905152 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835188 | CAAGCAATTATCCCA[C/T]CCCAGCCTCCCAAGT | 115677 |
rs767907928 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805998 | AGTAAAAGGAGGAAA[A/G]GATGGAGTAGACTAT | 115677 |
rs767920005 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819032 | TATTAGCTATGGTGG[C/T]AGTAGAATGGAAAGA | 115677 |
rs767924256 | snp | C/T | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851178 | TTGGCCAAACCCTGA[C/T]CACAGTGAGTAGAGA | 115677 |
rs767973435 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818086 | TAAAATTCCTTCTTA[A/G]TTTATAATGAAGGGA | 115677 |
rs768004839 | snp | G/T | 0.000264975 | 0.0115073 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859605 | CAACCCAGCCATCCT[G/T]GTAGTAATTCCATCT | 115677 |
rs768082064 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787168 | GAATAGTATTTGAAT[A/G]AGTCAAGTGGAAAGA | 115677 |
rs768082845 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830408 | AAGTGACCTTGTTCC[A/G]CATTCCAGACACATA | 115677 |
rs768104011 | snp | C/G | 1.66554e-05 | 0.00288573 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834277 | TGAAGCACTTTTCCA[C/G]CTTGTAGAAAGCTCC | 115677 |
rs768132604 | snp | G/T | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856761 | AGCCAGAAAGACACA[G/T]CAGCGTTAATGGATG | 115677 |
rs768138414 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811131 | TATCTCAGACAAGAA[A/G]GGCTCACTCTAATGG | 115677 |
rs768222859 | snp | C/G | 1.8396e-05 | 0.00303277 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834366 | CATGTGCCATAGAGA[C/G]GGATGGACTTGCTGC | 115677 |
rs768235576 | in-del | -/TCTC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826417 | TTACTTCTAATTCTT[-/TCTC]TCTTTCTTTCTTTCC | 115677 |
rs768243315 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797248 | GTACGTACCACCATG[C/T]CTGACTAGTTTTTTT | 115677 |
rs768258322 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843130 | CAGGTAAGTTATATA[C/T]TCACATTTTTTTCTT | 115677 |
rs768302112 | snp | C/T | 1.65809e-05 | 0.00287926 | stop-gained, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856698 | TTTTCAGGCCTGGAA[C/T]GAATGCTTAAAACGT | 115677 |
rs768305746 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793603 | GTGACAGAGTGAGAC[C/T]CTGTCTCAAAAAAGA | 115677 |
rs768306615 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854124 | TCCACCCACCTTGGC[A/C]TCCCAAAGTGCTGGG | 115677 |
rs768391757 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854494 | AATCCTTGAAATAAT[A/G]CATGTGAAAGCTCAG | 115677 |
rs768396075 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850051 | CTGAGTAGCTGGGAT[C/T]ACAGGCGTGTGCCAC | 115677 |
rs768457219 | in-del | -/AGTC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789985 | ATGCCGCTGGTTTTT[-/AGTC]AGGCCACAGTGAGAA | 115677 |
rs768501454 | snp | A/G | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865633 | AGGGCAATCAGGCAG[A/G]AGAAGGAAATAAAGG | 115677 |
rs768525322 | snp | C/T | 0.000282681 | 0.0118853 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824621 | TCCTATTTAACTAGT[C/T]CTTTTCTAACAGGGC | 115677 |
rs768583694 | in-del | -/A | 1.65641e-05 | 0.00287781 | frameshift-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859550 | GAAGCGAACTCCTAC[-/A]AAACTGTCATCAATG | 115677 |
rs768612829 | snp | A/G | 3.31791e-05 | 0.00407289 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828127 | AGGAAAATGACACTC[A/G]CCTTTGTTCCCCACT | 115677 |
rs768673589 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858938 | ATATCAAGAACAGAC[A/C]GAGACTAGGAGTGTA | 115677 |
rs768690261 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790805 | ATTTCCTGCTTTTGA[C/T]GGTTGTATTTTGGTT | 115677 |
rs768734661 | snp | A/G | 0.000132776 | 0.00814679 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828480 | TCAAGTCCTAAATGT[A/G]CAAGAGAAGAAGAGA | 115677 |
rs768750258 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815868 | CTCTTCTCCAAAGCT[C/G]GTCCTCCTTCTGGGA | 115677 |
rs768801822 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819161 | GATTAGCTCTGCTCT[C/G]TCTACTCCCCTTGCA | 115677 |
rs768803484 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814416 | AAGGCAGATTCCCAC[C/T]AGCTATCTAGAAATG | 115677 |
rs768865969 | snp | A/G | 1.97771e-05 | 0.00314455 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802705 | GGTTTGTGTGCCTGC[A/G]TGTGAGGAGGGTGGA | 115677 |
rs768886542 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822433 | AGGGCTGTCTTTCTT[A/T]GCTCAGTCTATGCCA | 115677 |
rs768904070 | in-del | -/AGC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815313 | TAGCCAGAGAAACAT[-/AGC]AGCTCCTAGAATGCC | 115677 |
rs768928716 | snp | G/T | 3.40507e-05 | 0.00412604 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855352 | TCTTTTTTCCTAAAG[G/T]AAGAAGATCCTAACA | 115677 |
rs768966290 | snp | C/T | 6.65569e-05 | 0.00576836 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851331 | ACATTGAAAAAGATA[C/T]CCAGGCTGTAATGGA | 115677 |
rs768969901 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853003 | TAATAAAAATGCCCC[-/T]ATCAAATAACTTGTC | 115677 |
rs768972340 | in-del | -/AAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807593 | TCTGATCGCTAAATT[-/AAC]AACAAGTATGAAGAT | 115677 |
rs769034623 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842842 | TTTTTCTTATAAAGA[C/T]CTTTCATTTTGTCAA | 115677 |
rs769063671 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809630 | TCACAATTTGAAAAT[A/G]CTCCCTTAAACTTTC | 115677 |
rs769094358 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790686 | AAAGAAACATAGTGA[C/T]TGAATGCCAGGCACA | 115677 |
rs769102726 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820784 | TCATACCACCAAAGC[C/G]CAACTTTTTTTTCCT | 115677 |
rs769119808 | snp | A/C | 8.29236e-05 | 0.00643855 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862046 | GAGTTGAATTTGGAA[A/C]AGGGTAAGAATCATT | 115677 |
rs769132910 | snp | C/T | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863793 | AAACAATCAAAAACA[C/T]CAGCATGTGAAACCC | 115677 |
rs769194084 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840931 | TGTAATTTTTACAAG[C/T]ATTTCAGGTCATTTC | 115677 |
rs769236392 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833884 | GCTGTGATATCTTCT[C/G]TGGTAAAGCCATTAT | 115677 |
rs769245307 | snp | A/G | 1.95364e-05 | 0.00312535 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802649 | GACACATTTCAACAT[A/G]AGGGACCCACTGACA | 115677 |
rs769272771 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850291 | ACCTAAAAGTCATAA[A/G]TCTAATAATGAAACT | 115677 |
rs769277032 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830038 | CAGAATGGATGCTCT[A/T]TTCAGAGTTTCGGGT | 115677 |
rs769287327 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847120 | TGAAATAATTAAAGT[A/G]GTATTTTCAGAGACT | 115677 |
rs769316240 | snp | G/T | 0.00021538 | 0.0103751 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861956 | ACAGCTTTATCTATT[G/T]CAGCCCCTGGTGCAG | 115677 |
rs769329503 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818514 | TACAGTTTGTTTTTT[A/G]AACTACTTTTCATTA | 115677 |
rs769331049 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831060 | GCTAGTACTGTGACT[A/G]TCTTAGTTCAGGCTG | 115677 |
rs769335251 | snp | G/T | 2.16701e-05 | 0.00329159 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802725 | AGGAGGGTGGAGGGT[G/T]GATTTGTATATTAAT | 115677 |
rs769433893 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825460 | TATATTTTCTCTACT[C/T]TATGGCTTTTGACAA | 115677 |
rs769439459 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843282 | ATTGTTTCAGTTTCT[C/T]CATGGATACAATTAC | 115677 |
rs769445435 | snp | A/G | 1.95071e-05 | 0.003123 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834377 | GAGAGGGATGGACTT[A/G]CTGCCCTTAGCTACG | 115677 |
rs769492044 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861604 | GGGATGATGATAACA[G/T]GCACATGCCCCAAAT | 115677 |
rs769623767 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839400 | ACTCTATCAGCACAC[A/G]AGATGGTAATGGTCT | 115677 |
rs769641432 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798254 | TGGGCTCATATTACC[A/G]TAAAGTATTTAACTA | 115677 |
rs769647934 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800929 | AAAAAAACAAAAAAA[A/G]AGATGGGGTGTTGCT | 115677 |
rs769691288 | snp | A/G | 1.65855e-05 | 0.00287967 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856783 | TAATGGATGAGGTAA[A/G]TGTTTGCCGAGTGCA | 115677 |
rs769716897 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806720 | GCATATTAATATGAA[C/T]TCATATGGAGATGTA | 115677 |
rs769744946 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794876 | CTGGGATTGCAGGTG[A/T]GCCACTGCACCTGGC | 115677 |
rs769780100 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850295 | AAAAGTCATAAGTCT[A/G]ATAATGAAACTTCTG | 115677 |
rs769823691 | snp | C/T | 1.65671e-05 | 0.00287807 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860854 | GAAGAGATTAGAGAA[C/T]ATTGTGAGCAAGGCA | 115677 |
rs769829052 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815404 | AAGGTACATTCTCAG[A/C]AACACTTTGTGAATG | 115677 |
rs769865034 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862479 | ATTAGAGATGTACCC[C/T]ACCTTTTTATTTTTT | 115677 |
rs769976247 | snp | G/T | 5.09178e-05 | 0.00504542 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850981 | TCAAGAGGCTAATCA[G/T]GAGACTTTGTTCAGT | 115677 |
rs769988812 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816962 | TGTCAAAAACATTTA[A/C]TGGCATAATATGTAG | 115677 |
rs770015820 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859140 | CACAATATTTAGCAC[C/T]GATGGCTCACCTTCT | 115677 |
rs770123142 | snp | A/G | 1.66574e-05 | 0.0028859 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828501 | GAAGAAGAGAAAATC[A/G]GTGAGTCCAAACCTT | 115677 |
rs770185386 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834205 | GCTCCTTTTTTTCTT[A/G]TTTGTATGTTTTTTA | 115677 |
rs770209054 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835614 | TTAACCTAACTGGAG[C/T]CAGAAAATGTCTGTA | 115677 |
rs770250235 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855295 | GTATCAGAATGGACA[A/G]GGAATAGCAACTCTT | 115677 |
rs770262888 | snp | C/T | 1.67699e-05 | 0.00289563 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855366 | GGAAGAAGATCCTAA[C/T]AGTGCAATGGATAAA | 115677 |
rs770275356 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812595 | CAGTGGCTTAGGGGT[C/T]ATGCTTAAATAGTAT | 115677 |
rs770306756 | snp | A/C/T | 4.35088e-05 | 0.00466399 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811663 | CAAAGGTACAAAATG[A/C/T]ACGTTTGCAATAAAT | 115677 |
rs770324602 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823301 | GATTACAGGCGTGAG[C/T]CACCGCGCCCGGCCA | 115677 |
rs770343249 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793154 | ATCACCCAGTCTTGC[C/T]GGTTCCATTTTAAAA | 115677 |
rs770352848 | snp | A/G | 1.68332e-05 | 0.00290109 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855456 | AGCCTCAAAAGACAA[A/G]GAAGGTGTGTAACCA | 115677 |
rs770378694 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841033 | TGAGGTAGACAGATC[A/G]CTTGAGCCCAGGAGT | 115677 |
rs770379512 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822594 | AACTCTTAGGATCTA[C/T]ATTAAAAAGGAAAAC | 115677 |
rs770409424 | snp | C/T | 5.00513e-05 | 0.00500231 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855388 | ATGGATAAAGAGAGA[C/T]GAAAGTCTTTACTAA | 115677 |
rs770453222 | snp | A/T | 4.97228e-05 | 0.00498587 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864840 | TTTTCACAGGTGACA[A/T]TGTGATTATACACGA | 115677 |
rs770457250 | snp | C/T | 1.6884e-05 | 0.00290547 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851394 | CTGAGTTCCTGTTAA[C/T]GGATTACTTTGTGAG | 115677 |
rs770494944 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845475 | GGGTCCTACCTGGTG[C/T]AGCTGATAACTAGCT | 115677 |
rs770525105 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818713 | TTGACTTATCAATTG[A/G]CCTTCATTATTACTA | 115677 |
rs770525304 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832349 | TCTAGAACAATGTAG[C/T]ATAGGAGGAATTCAT | 115677 |
rs770528233 | snp | C/T | 3.31334e-05 | 0.00407009 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864904 | GAATGGGAAAAAAGG[C/T]CATTTTCCTGCCGCT | 115677 |
rs770538418 | in-del | -/CTT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859151 | GCACTGATGGCTCAC[-/CTT]CTTCGCAGACCACCA | 115677 |
rs770556256 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804578 | CAAATGAGTGCCTCA[G/T]GAAACATTTAGGTAG | 115677 |
rs770580135 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831281 | GGGTCTCTTTTATAA[A/G]GGCACTAATCTCATT | 115677 |
rs770628575 | snp | G/T | 3.75749e-05 | 0.00433429 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811531 | GCTCGTAATCTTCCT[G/T]TTCATTGTTTTTTTG | 115677 |
rs770660793 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796801 | TTTAGAGTTCCTGCC[A/C]AGAAGGTCACACTTA | 115677 |
rs770664111 | in-del | -/CGCGCGCACACA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834502 | GCGTGCGCGCGCGCG[-/CGCGCGCACACA]CACACACACACACAC | 115677 |
rs770713910 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809021 | TTATGTTATGAAACA[C/T]AAAAGTGTTTCATAA | 115677 |
rs770741701 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851836 | GGGTCAGGAATTCAG[C/T]TGTGTCTTAGCCAGG | 115677 |
rs770824488 | snp | C/G | 1.66407e-05 | 0.00288446 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843100 | AAATGGGAAAACACA[C/G]TAGAGAACTGCTACC | 115677 |
rs770913882 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823422 | TGGCAGTCAGAGGTG[C/T]GTTCTGAGGGCTGTG | 115677 |
rs770955731 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839545 | TTCCAAGAGCAAAAA[A/G]AGGGACGAAAGGAAA | 115677 |
rs770979192 | snp | A/G | 9.94514e-05 | 0.00705094 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861932 | GCCTGCTAACACAGC[A/G]TACTAATTACAGCTT | 115677 |
rs771024963 | snp | A/C | 4.96866e-05 | 0.00498406 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851129 | CAACTTTTATGCAAT[A/C]ACTTAAACCAGTACA | 115677 |
rs771094519 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822929 | TTTATTGCCAACGAT[G/T]ATAATCTAGAGCTAA | 115677 |
rs771156726 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848391 | AATTGGGCAGCTTCA[C/G]AGGCAACTAAGAAGA | 115677 |
rs771159389 | in-del | -/TTTTGT | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823008 | TACTAGTTGTATTAC[-/TTTTGT]TTTTGTTTTTGTTTT | 115677 |
rs771161171 | in-del | -/AAAGCAATTGAATTG | 1.65921e-05 | 0.00288024 | cds-indel, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828430 | TCCAGAAAACTTGGC[-/AAAGCAATTGAATTG]GAAGCAATAAAACCG | 115677 |
rs771170222 | in-del | -/TT | 3.11881e-05 | 0.00394881 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811556 | TTTTTGTTATTGTTC[-/TT]GTTTTTCAGTATAAT | 115677 |
rs771175678 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797428 | ACACAATAAGATAAA[A/C]AAAGTAAAAGAGGTG | 115677 |
rs771217628 | in-del | -/ACACACACACACAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834502 | CGTGCGCGCGCGCGC[-/ACACACACACACAC]GCGCGCACACACACA | 115677 |
rs771234726 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857212 | TACCTCATGGGGCTT[C/T]TGTGAGGGTGAAATA | 115677 |
rs771238952 | in-del | -/CACACACACACC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834541 | ACACACACACACACA[-/CACACACACACC]CCACATACATTTTAA | 115677 |
rs771292680 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787010 | CTGGGATTACAGGCG[A/T]GAGCCACCACACCCG | 115677 |
rs771320607 | snp | A/G | 4.97946e-05 | 0.00498947 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860926 | TAATCCCATGCCCAC[A/G]ATCATTTTGGCCTGG | 115677 |
rs771365543 | snp | A/G | | | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855402 | ACGAAAGTCTTTACT[A/G]AAACCAAAATTATTG | 115677 |
rs771389433 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801498 | AAAGTGCTTGGATTA[C/T]ATGCATGAGCCACTG | 115677 |
rs771411241 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822752 | ATGATTCAATCTATC[C/T]AAAAGAACCAAGGGG | 115677 |
rs771439890 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856500 | GAATTGTTTGAACTT[A/G]GGAGGCAGAGGTTGC | 115677 |
rs771444178 | in-del | -/A/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820717 | AGGAGAAAAGCTGGC[-/A/AA]CAAAAAAAAAAAAAG | 115677 |
rs771444306 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814182 | ATACAGGCCACTTCA[C/T]TTCTCAGGGCTGGAT | 115677 |
rs771444416 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800322 | TGGGTTTCTGTTTGT[A/T]ACACAGCATTATTGT | 115677 |
rs771457799 | snp | A/G | 0.000308578 | 0.0124175 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855471 | GGAAGGTGTGTAACC[A/G]TCTCTTTGAATGGCC | 115677 |
rs771476789 | snp | A/C | 1.70266e-05 | 0.00291771 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855468 | CAAGGAAGGTGTGTA[A/C]CCATCTCTTTGAATG | 115677 |
rs771497524 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812947 | GGCCAAAGAAAGATA[C/T]GAGCGAGCTGAAACA | 115677 |
rs771533891 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795932 | CTTCCATCCTGAGGC[G/T]GTGGGCAAAGGCCGA | 115677 |
rs771540997 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797188 | CGATTTCCCCAAGCT[A/C]AGGTGATCCTCCCAC | 115677 |
rs771545498 | snp | C/T | 4.97929e-05 | 0.00498939 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831517 | CTTGTCATTAGCAAC[C/T]GGAATCAGCAAATTA | 115677 |
rs771551042 | snp | A/C | 1.66112e-05 | 0.00288189 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864993 | CTCTGAACATACTAC[A/C]TTCACACTCGGTAAT | 115677 |
rs771566258 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820627 | CCCAACACAAGAAGT[A/G]CTGTGTGGTAGTTGA | 115677 |
rs771587466 | in-del | -/T/TT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838789 | AAATAAAAAAAACTC[-/T/TT]TTTTTTTTTTTTTTT | 115677 |
rs771594120 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809325 | AAGAGGGCAAACAAG[C/G]CTTTACTGAAACCTC | 115677 |
rs771596668 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852969 | GTACAATAAAATAAA[C/T]CTATTTTCTTACAAA | 115677 |
rs771647803 | snp | A/T | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863556 | TGGAATTCTCTTTAT[A/T]TGAATCATTGCTTTA | 115677 |
rs771678163 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864431 | GCTGGTATTACAGGC[A/G]TGCGCCACCACACCC | 115677 |
rs771678871 | snp | C/T | 1.66034e-05 | 0.00288122 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856687 | ACATGATTTCATTTT[C/T]AGGCCTGGAACGAAT | 115677 |
rs771745688 | snp | C/T | 0.000281608 | 0.0118628 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864916 | AGGCCATTTTCCTGC[C/T]GCTTATGTGGAGGAG | 115677 |
rs771758100 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804401 | CAGCCTGGGTTTCCA[A/G]ACCCTCTAAACTCAC | 115677 |
rs771765578 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839639 | GAGTCTACAGCCGGG[A/C]GCAGTGGCTCAGGCC | 115677 |
rs771834900 | snp | A/G | 1.66418e-05 | 0.00288455 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824614 | CAGTACATCCTATTT[A/G]ACTAGTCCTTTTCTA | 115677 |
rs771843065 | in-del | -/ATCA | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863847 | GTTTGGTGACAATCC[-/ATCA]ATCAGCTACATAGAA | 115677 |
rs771874331 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804899 | AATAAAAATCAGAAA[-/T]TTTTATGATAACATT | 115677 |
rs771976349 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859354 | TAAAGAGTTTATTCC[G/T]CCATTTTTTTTTCCT | 115677 |
rs771979938 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817649 | AATGCACACTTTAGG[C/G]TCTGAAGTTCTAGAG | 115677 |
rs772031272 | snp | C/G | 4.96923e-05 | 0.00498434 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851101 | CATTCTGGAGCTGGA[C/G]AAGGAAAGAATTCAA | 115677 |
rs772034983 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829539 | TTGGTCAGGCTTGTC[C/T]CCAACTCCTGACCTC | 115677 |
rs772056188 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798276 | ATTTAACTAGGTCTC[A/C]ATTGATGATGTTCAT | 115677 |
rs772086932 | snp | G/T | 1.66391e-05 | 0.00288431 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851327 | ATTGACATTGAAAAA[G/T]ATATCCAGGCTGTAA | 115677 |
rs772088308 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827813 | CTGTGGCCTCAAGTG[A/C]TCATCCCACCTCAGC | 115677 |
rs772098813 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791938 | TTGTGTAGGTTGCCT[A/G]TTCACTCTGATGGTA | 115677 |
rs772108172 | snp | A/C | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784643 | CCAAGATTTCTACTG[A/C]ATTTCAAATTCTCCA | 115677 |
rs772139232 | snp | C/T | 3.40686e-05 | 0.00412713 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860757 | AATGTTTATGATAAT[C/T]GTGTTACAAAATATG | 115677 |
rs772178978 | snp | A/G | 3.337e-05 | 0.00408459 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828373 | ATTTGGAAAGTAGAT[A/G]TAAACGCTGATATTA | 115677 |
rs772231940 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838519 | TACTGGGATTACAGG[C/T]GCGAGCCACCGTGCC | 115677 |
rs772260062 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790475 | GAAATGAGTCACGTG[A/G]ATGAATGCAATAAAG | 115677 |
rs772284642 | in-del | -/T | 1.67279e-05 | 0.002892 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831587 | TTTAGAATTGAAGTG[-/T]TTTGCTTTCATACAA | 115677 |
rs772318247 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833678 | CTTCCTTCCCTACTT[C/G]TTTCTACTTCTCCAA | 115677 |
rs772341182 | snp | C/T | 1.65638e-05 | 0.00287778 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862018 | GTATTCTTTTCAAGC[C/T]AGGCAAGATGATGAG | 115677 |
rs772350886 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838575 | TTTGCTTTTGTCTAT[C/G]TCCACTGCTGACATC | 115677 |
rs772376383 | snp | C/T | 1.65756e-05 | 0.00287881 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861939 | AACACAGCATACTAA[C/T]TACAGCTTTATCTAT | 115677 |
rs772380239 | in-del | -/TGAG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816868 | GAAGGCACTCATGTT[-/TGAG]TGACTCTGCCTTGAA | 115677 |
rs772400477 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794809 | CATGTTGCCTAGGCA[C/G]GTCTCAAACTCCTGG | 115677 |
rs772407989 | in-del | -/A | 1.65688e-05 | 0.00287821 | frameshift-variant, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856722 | AAAACGTACTCCAGC[-/A]CCTCCTCCTTCTCTG | 115677 |
rs772479989 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819794 | GAGAAAGGGTACAAT[C/T]GTGCTGTTCAGAGAG | 115677 |
rs772537124 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832746 | TTGCTTTTTAGTTTT[C/G]CCATGGATTTTATGA | 115677 |
rs772546809 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789702 | GGCTACTACTATCAC[A/C]ACCAATGCCATGGAA | 115677 |
rs772551514 | in-del | -/CACACACGCG/CACACACGCGCG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834511 | GCGCGCGCGCGCACA[-/CACACACGCG/CACACACGCGCG]CACACACACACACAC | 115677 |
rs772612020 | snp | C/T | 2.01428e-05 | 0.00317348 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802613 | CAGAATGCTGGAGCG[C/T]AGGTGAAAGGACAAA | 115677 |
rs772624623 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840543 | TCAAAAAAAAAAAAA[A/C]AAAAAAAACAAAAAA | 115677 |
rs772669585 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845748 | GCATCTTTCAACTTC[A/C]GCTCTAAAAATATTT | 115677 |
rs772703692 | snp | A/G | 1.69815e-05 | 0.00291384 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842942 | TATGGAATTACAAAG[A/G]GCTTTCAAAAATGTG | 115677 |
rs772705309 | snp | C/T | 3.93229e-05 | 0.00443395 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811519 | ATCTTCGGAGTTGCT[C/T]GTAATCTTCCTGTTC | 115677 |
rs772724370 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857741 | TAAATTTTTTAGCAA[A/T]GTTTTGAAGGTACAG | 115677 |
rs772744309 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786204 | CAGACATCAGCAGGC[C/G]AGGAGAGGGCTGCAC | 115677 |
rs772841902 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831069 | GTGACTGTCTTAGTT[A/C]AGGCTGCTCTAACAA | 115677 |
rs772851114 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861636 | TCCCGTATTTATACC[C/T]GAATGGCAAAACTGG | 115677 |
rs772871201 | in-del | -/GTATACT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828841 | GGGATTTTTTTCACA[-/GTATACT]GCTAAATAAAGCAGA | 115677 |
rs772890682 | snp | A/C/T | 3.31314e-05 | 0.00406999 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828208 | GAATGAAATCCACAG[A/C/T]GGACCTGCATCAGTG | 115677 |
rs772894740 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817948 | GATGGTCTTTCAAAA[C/G]ACATACCAATGAAGT | 115677 |
rs772901299 | snp | C/T | 1.94426e-05 | 0.00311784 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802657 | TCAACATGAGGGACC[C/T]ACTGACAGATTGTCC | 115677 |
rs772918355 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800232 | TACATGAGTGAGGTC[A/G]GGGGACACCTGAAGA | 115677 |
rs772925643 | in-del | -/TATATAG | 1.67545e-05 | 0.0028943 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843113 | ACTAGAGAACTGCTA[-/TATATAG]CCAGGTAAGTTATAT | 115677 |
rs772969460 | snp | A/G | 4.97863e-05 | 0.00498906 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843066 | CCAAAAAAACATGGC[A/G]GGTTATTCTACCAGA | 115677 |
rs772970522 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798262 | TATTACCATAAAGTA[A/T]TTAACTAGGTCTCAA | 115677 |
rs773071213 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787347 | CATGCCTGTGACAGC[C/T]CCAGGACTCTGGCCA | 115677 |
rs773088398 | in-del | -/A | | | intron-variant, frameshift-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863414 | GTGAAAGGAAGACTG[-/A]AAAAATCACCTCAGA | 115677 |
rs773132927 | snp | A/T | 1.66579e-05 | 0.00288595 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828143 | CCTTTGTTCCCCACT[A/T]TTTTTTGCCTTTAGT | 115677 |
rs773196182 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785611 | ATTAAGTCAATAAAT[A/G]TATTGAGCACCAATC | 115677 |
rs773224928 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846604 | CCCACCCTCCAAGAA[G/T]AAACACTTCAGATGA | 115677 |
rs773227046 | in-del | -/GAC | 1.6869e-05 | 0.00290417 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860771 | CGTGTTACAAAATAT[-/GAC]GACTTTTTATGTCAT | 115677 |
rs773258714 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795031 | GCTGTCACAGGAAAA[A/T]ATCACAATAAATAAC | 115677 |
rs773268786 | snp | A/C/T | 0.000182225 | 0.00954365 | missense, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856728 | TACTCCAGCACCTCC[A/C/T]CCTTCTCTGATGCAA | 115677 |
rs773290300 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834025 | ACAAAGTGTTAGCTG[C/T]TCTGATGTTTTAGGT | 115677 |
rs773294973 | snp | C/G | 0.000149099 | 0.00863292 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860860 | ATTAGAGAATATTGT[C/G]AGCAAGGCATCTTCT | 115677 |
rs773303748 | snp | A/G | 1.65798e-05 | 0.00287917 | splice-acceptor-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864833 | AACTGTATTTTCACA[A/G]GTGACATTGTGATTA | 115677 |
rs773335250 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816974 | TTACTGGCATAATAT[A/G]TAGCATATTATTTTG | 115677 |
rs773345239 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847356 | ACAATGTCTCAAAGC[A/G]CCTGGGGTGCTTAAA | 115677 |
rs773371532 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821293 | GTGTGCTCTAACATC[A/G]GGGCTGAGCACCCAA | 115677 |
rs773374072 | snp | C/T | 1.66896e-05 | 0.00288869 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860786 | TGACTTTTTATGTCA[C/T]TTGAACAGGAGCATA | 115677 |
rs773399739 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804369 | TCCGGGAGTCATGGG[A/G]AGGGCGGATATCCCT | 115677 |
rs773504731 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798735 | AGAGAACTCAAAAGG[A/T]CTCTTTGTGCATTAA | 115677 |
rs773541469 | snp | C/T | 1.65726e-05 | 0.00287855 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864847 | AGGTGACATTGTGAT[C/T]ATACACGAGAAAAAA | 115677 |
rs773547063 | in-del | -/GCGTGCGCGCGCGC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834487 | TCCAAATCATTACTG[-/GCGTGCGCGCGCGC]GCGCGCGCACACACA | 115677 |
rs773553754 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855180 | TTTTCTTATTCATCA[-/G]GTCTCGAACAGGTAG | 115677 |
rs773556647 | in-del | -/GGAGGGT | 2.01019e-05 | 0.00317026 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802710 | TGTGCCTGCGTGTGA[-/GGAGGGT]GGAGGGTGGAGGGTG | 115677 |
rs773579519 | in-del | -/TCT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795558 | ATCTATTTGGTTTCC[-/TCT]TCTTTCTCCATTAAC | 115677 |
rs773588450 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855299 | CAGAATGGACAGGGA[A/C]TAGCAACTCTTACTT | 115677 |
rs773635798 | snp | A/T | 1.66183e-05 | 0.00288251 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828412 | TGTCTTTTATGTTTT[A/T]TTTCCAGAAAACTTG | 115677 |
rs773671245 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808099 | TAAAAATGTGTCTTA[-/G]GGGAGTTTTGATGGC | 115677 |
rs773693499 | in-del | -/GTAGAACAAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855192 | TCAGGTCTCGAACAG[-/GTAGAACAAT]GTGTGTAAAACTAAA | 115677 |
rs773702640 | snp | A/G | 1.66724e-05 | 0.0028872 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828505 | AAGAGAAAATCAGTG[A/G]GTCCAAACCTTTCTT | 115677 |
rs773704017 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842009 | TCCTGCTGGGAATGG[A/G]GCAGGATCCTCTCTG | 115677 |
rs773751937 | snp | C/T | 6.62723e-05 | 0.00575602 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864913 | AAAAGGCCATTTTCC[C/T]GCCGCTTATGTGGAG | 115677 |
rs773768020 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812749 | GCACCACCATCTCTG[A/G]GCAGATAAGCAAGTG | 115677 |
rs773807505 | snp | G/T | 0.000139621 | 0.0083541 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811541 | TTCCTGTTCATTGTT[G/T]TTTTGTTATTGTTCT | 115677 |
rs773816220 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854427 | TGTCCCTCTGCCACT[C/G]ATGTTTAGCAACCTC | 115677 |
rs773874293 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810107 | GCCTCACCAGTTCAC[A/G]GTCCTCACCCTCCTC | 115677 |
rs773890772 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822642 | TAATTCCCTACATTT[G/T]TATTCTCTATAGTCA | 115677 |
rs773898904 | snp | A/C | 1.67237e-05 | 0.00289164 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855372 | AGATCCTAACAGTGC[A/C]ATGGATAAAGAGAGA | 115677 |
rs773906529 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807958 | CCCTTACTTTAAGAG[A/G]TTGAATGTGAATGCC | 115677 |
rs773928664 | snp | A/G | 5.00413e-05 | 0.00500181 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855389 | TGGATAAAGAGAGAC[A/G]AAAGTCTTTACTAAA | 115677 |
rs773952070 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838910 | TGCCTTAGCCTCCCA[A/G]GTAGCTGGGATTACA | 115677 |
rs773971915 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819760 | TAAACCCTTCGGGGT[C/T]ATCAATAAGTTGCAG | 115677 |
rs773999582 | snp | A/G | 1.67973e-05 | 0.00289799 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843116 | TAGAGAACTGCTACC[A/G]GGTAAGTTATATATT | 115677 |
rs774026411 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818821 | TCCTTGGTCCAGAAC[A/C]TTTTTTAGCATATTA | 115677 |
rs774111314 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862707 | ATTACGTAGTGGCTT[C/T]ATAATGTAAACCACA | 115677 |
rs774130632 | in-del | -/T | 1.65732e-05 | 0.00287859 | frameshift-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862039 | AGATGATGAGTTGAA[-/T]TTGGAAAAGGGTAAG | 115677 |
rs774135669 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816180 | GCCTTTTACTCTGAC[A/T]GAGCTGTGCCCCTTT | 115677 |
rs774163807 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788658 | GGTTACATAGGGGAG[A/G]ATTGATCAAAGGCGT | 115677 |
rs774172383 | in-del | -/GTAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862543 | CTCTCTCAACTTAGT[-/GTAA]GTAAGTAAGTGCAAA | 115677 |
rs774234783 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811884 | GGCTCAGTCAAGTCT[C/T]TTCTGATTCCTCAGA | 115677 |
rs774253240 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850658 | TGGCTCATGCCTGTA[A/G]TCCTAGCACTTTGGG | 115677 |
rs774293047 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796849 | TTGAACTCTGCTTCC[A/T]GATAGCTGAGGATAT | 115677 |
rs774378965 | snp | G/T | 1.66585e-05 | 0.00288599 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856808 | AGTGCATTTCCTAGA[G/T]GTAGTGATGAAAAGG | 115677 |
rs774384593 | snp | C/T | 1.6825e-05 | 0.00290038 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842975 | AGTAAATGTGTGACA[C/T]TGATGTTTTACATTA | 115677 |
rs774389665 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793424 | ACCAGCCTGGGCAAT[A/G]TGGTGAAACCTCATC | 115677 |
rs774423477 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823481 | TGGCTCCTGATGATT[C/T]GCTGGCAATCTTTGG | 115677 |
rs774441157 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805539 | AAGTATTAATAGCAC[C/T]TTCCTATCAAACAAT | 115677 |
rs774466918 | snp | A/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859555 | CGAACTCCTACAAAC[A/T]GTCATCAATGTTAGC | 115677 |
rs774510682 | snp | C/G | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860874 | TGAGCAAGGCATCTT[C/G]TGGTGGGCAGAGCAA | 115677 |
rs774530571 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815857 | GGGTTTATCCACTCT[C/T]CTCCAAAGCTGGTCC | 115677 |
rs774598528 | snp | C/G | 1.65627e-05 | 0.00287769 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851143 | TAACTTAAACCAGTA[C/G]AGCCAACATATTTCT | 115677 |
rs774622286 | in-del | -/A | 1.6599e-05 | 0.00288084 | splice-donor-variant, intron-variant | NOSTRIN | GRCh38.p7 | 2:168824717 | GAACACGAGAAAAAG[-/A]GTAAGTATTGTGGCA | 115677 |
rs774645154 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831297 | GGCACTAATCTCATT[C/T]ATGGGGGCTCCACCC | 115677 |
rs774676981 | snp | C/T | 1.70624e-05 | 0.00292077 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855469 | AAGGAAGGTGTGTAA[C/T]CATCTCTTTGAATGG | 115677 |
rs774687363 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795986 | AATATGTGCATTAAG[A/G]CAAGGCTTCAGAAAT | 115677 |
rs774704823 | snp | A/G | 1.66139e-05 | 0.00288213 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860799 | CATTTGAACAGGAGC[A/G]TACTCATAGCTATGT | 115677 |
rs774716052 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844727 | TAGAAAAAATTAGCC[A/G]CGCGTGGTGGCGGGC | 115677 |
rs774728298 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801991 | CTGAACATTCTATAG[-/T]TATAGTTCTATAGGT | 115677 |
rs774737033 | in-del | -/C | 1.65996e-05 | 0.00288089 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831497 | AAGTTGAAAAGACAG[-/C]AAATCTTGTCATTAG | 115677 |
rs774741246 | in-del | -/GG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816018 | TTCTTTTTATTTTAT[-/GG]CCTCTTCCACTGTTC | 115677 |
rs774746395 | snp | C/T | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855889 | TTCTGTACGTAGAAG[C/T]TAGGCATGTCAGACT | 115677 |
rs774771395 | in-del | -/ACAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834512 | CGCGCGCGCGCACAC[-/ACAA]ACACACACACACACA | 115677 |
rs774920294 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822760 | ATCTATCCAAAAGAA[C/T]CAAGGGGTTTGCTTT | 115677 |
rs774920589 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787122 | CTGGGATCAGGTAAG[A/G]AAAGGTTTCAAGCAG | 115677 |
rs774924808 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801507 | GGATTACATGCATGA[A/G]CCACTGCAACTGGCT | 115677 |
rs774966218 | snp | A/G | 3.31939e-05 | 0.0040738 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856690 | TGATTTCATTTTCAG[A/G]CCTGGAACGAATGCT | 115677 |
rs774972955 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843571 | TCTCAGTGGCAAAAG[C/T]AGACACATAAAGAAG | 115677 |
rs774974154 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800362 | TAAACGATACCAACC[C/T]ATTTCTGACCTCCAA | 115677 |
rs775043671 | snp | C/T | 1.65979e-05 | 0.00288074 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831513 | AAATCTTGTCATTAG[C/T]AACTGGAATCAGCAA | 115677 |
rs775047793 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856523 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 115677 |
rs775069989 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845991 | CTCTGAGTTCTCTCC[G/T]GCCTCCTGAGAGCCA | 115677 |
rs775084411 | snp | C/T | | | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826605 | AAGGGGGAGCATCTC[C/T]ATTCAGACACAGACT | 115677 |
rs775103309 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809408 | AGATCAAAGGGGGAG[C/G]GAGGCTGAGAAATGA | 115677 |
rs775156179 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808067 | GCCTCCTAAAACTAG[C/T]TCCCTTGAGACAGTA | 115677 |
rs775176252 | in-del | -/TT/TTT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797079 | TCTTTTTCTTTTTTC[-/TT/TTT]TTTTTTTTTTTTTTT | 115677 |
rs775241960 | in-del | -/GT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859720 | ATCAGGGCAAAAAAG[-/GT]GTTAGGAATTCTATG | 115677 |
rs775269129 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847433 | ATCAGAGCCTCTGAA[C/T]GATTATAAAGAGGGG | 115677 |
rs775271443 | snp | A/C | 1.65701e-05 | 0.00287833 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864857 | GTGATTATACACGAG[A/C]AAAAAGAAGGAGGAT | 115677 |
rs775387025 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790571 | CATCAGATAAGTCCA[A/C]ATTGAAGGACGTTAC | 115677 |
rs775417955 | snp | C/T | 2.21334e-05 | 0.00332659 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811667 | GGTACAAAATGCACG[C/T]TTGCAATAAATGGTT | 115677 |
rs775457685 | snp | A/G | 3.40188e-05 | 0.00412411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860758 | ATGTTTATGATAATC[A/G]TGTTACAAAATATGA | 115677 |
rs775463064 | snp | A/C | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863857 | CAATCCATCAGCTAC[A/C]TAGAAATAGAAAGTG | 115677 |
rs775485165 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840531 | CGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 115677 |
rs775492907 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800468 | ATTCAGCTGGGATGC[C/T]CTGCTGCCCTTACAA | 115677 |
rs775528362 | snp | A/C | 1.70682e-05 | 0.00292127 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843133 | GTAAGTTATATATTC[A/C]CATTTTTTTCTTCTT | 115677 |
rs775539184 | snp | A/G | 1.66807e-05 | 0.00288792 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828377 | GGAAAGTAGATGTAA[A/G]CGCTGATATTATGCT | 115677 |
rs775544449 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813176 | CCATTATTTGTATGA[C/T]TCCTATGAATTCAAC | 115677 |
rs775593252 | in-del | -/AG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807282 | CATACACACACACAC[-/AG]AGAGAGAGAGAACTA | 115677 |
rs775601855 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827827 | GATCATCCCACCTCA[A/G]CCTCCTAAAGTGCTG | 115677 |
rs775614192 | snp | A/C | 2.46521e-05 | 0.00351076 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811574 | TTTTTCAGTATAATA[A/C]AGTATACAAGAACCT | 115677 |
rs775616115 | snp | A/T | 6.92065e-05 | 0.00588205 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850960 | TATGGTTTGGATATG[A/T]CATAGTCAAGAGGCT | 115677 |
rs775623768 | snp | A/T | 9.98236e-05 | 0.00706412 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851328 | TTGACATTGAAAAAG[A/T]TATCCAGGCTGTAAT | 115677 |
rs775665597 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857787 | GTTTTTCTTGCTTAT[A/G]GCCTAACTTTCTTGT | 115677 |
rs775678997 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851902 | ATCAGGTTGGGCTGC[A/T]GACATCTCCAGGCTC | 115677 |
rs775698997 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814379 | AAGTCAGAAATTCCT[C/T]CTCTAGATATACATT | 115677 |
rs775710247 | in-del | -/T | 0.000103006 | 0.00717582 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834213 | TTTCTTGTTTGTATG[-/T]TTTTTTACTCTAGGC | 115677 |
rs775721014 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823583 | TGTCTGTTTATGTCC[A/G]AATTTTCTCTTTATA | 115677 |
rs775752435 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788263 | AAAAAAAAAAGATGA[-/T]GATATTGATGACTTT | 115677 |
rs775757505 | in-del | -/CTT | 1.65669e-05 | 0.00287805 | cds-indel, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856730 | CTCCAGCACCTCCTC[-/CTT]CTCTGATGCAAAGAG | 115677 |
rs775793562 | snp | C/T | 3.32452e-05 | 0.00407695 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834250 | GAAATTAATGGTTAG[C/T]ACCAAGAAACATGAA | 115677 |
rs775843727 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851185 | AACCCTGACCACAGT[A/G]AGTAGAGATGATCTC | 115677 |
rs775847874 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862881 | TCCACGACAAGGACA[C/T]GGCTCCCAGAGCCAA | 115677 |
rs775934054 | snp | C/T | 3.31384e-05 | 0.00407039 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861948 | TACTAATTACAGCTT[C/T]ATCTATTTCAGCCCC | 115677 |
rs775999062 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860095 | CAGAAGGGGGAACTG[C/T]AATCATCTTGTGAAG | 115677 |
rs776107164 | snp | C/T | 1.86684e-05 | 0.00305513 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834370 | TGCCATAGAGAGGGA[C/T]GGACTTGCTGCCCTT | 115677 |
rs776107698 | snp | A/G | 1.66335e-05 | 0.00288383 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831551 | CAAGTATCCACAAAT[A/G]CCATTTGTGTAAACT | 115677 |
rs776154534 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858000 | GGTAACAGAGGTCTA[A/G]CATACCTGCAATGAC | 115677 |
rs776155575 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797346 | AAGCAACCCTTCTGC[C/T]ACAGCCTCCCAAAGT | 115677 |
rs776160376 | snp | C/T | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786032 | TGCTAGGATTACAGG[C/T]ATAAGCCACTGCACA | 115677 |
rs776182218 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845749 | CATCTTTCAACTTCA[C/G/T]CTCTAAAAATATTTA | 115677 |
rs776216885 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784757 | TCTTTTTGGCGTCAT[A/G]TTGTATAGTCCTTTC | 115677 |
rs776231484 | in-del | -/A | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865782 | AAAGTCTCAAGATAC[-/A]AAAATCAATGTGCAA | 115677 |
rs776247588 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843185 | TGAAGATGGAGGTCA[A/G]ATTACAGTGACAAGA | 115677 |
rs776294886 | snp | C/T | 1.66466e-05 | 0.00288496 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865015 | CTCGGTAATCAACAA[C/T]ACAGTGTGGTTCAAA | 115677 |
rs776308449 | snp | A/G | 3.34247e-05 | 0.00408794 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834288 | TCCAGCTTGTAGAAA[A/G]CTCCAAGCAATCTAT | 115677 |
rs776332943 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827963 | ACTGGGAAAAAAGCA[A/G]TATATATAATGAGTA | 115677 |
rs776354580 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811179 | GCCCCAGAAATATTA[C/T]TTTGAAGTTTATATG | 115677 |
rs776383262 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841585 | CATTGGGCATGTATC[C/T]CAGGCTTTTCACTGG | 115677 |
rs776411902 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785346 | AGTTCAAAAGGGTCC[C/G]TAGAGTTTTTAAGAG | 115677 |
rs776423986 | snp | C/G | 1.75971e-05 | 0.00296618 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855494 | GAATGGCCAGAAAAG[C/G]GACCATATGATGCTC | 115677 |
rs776548118 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836247 | GACCTGCCTAGGCAT[C/T]CTGAGTGCTCATTAG | 115677 |
rs776557281 | in-del | -/AGAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788896 | CACAGATAAAAAGAT[-/AGAT]AGATAGATAGATAGA | 115677 |
rs776585779 | snp | A/T | 1.65633e-05 | 0.00287774 | stop-gained, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859567 | AACTGTCATCAATGT[A/T]AGCAGAACTTGAGCA | 115677 |
rs776623090 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850057 | AGCTGGGATTACAGG[C/T]GTGTGCCACCATGCC | 115677 |
rs776628499 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805942 | TGAGATGTGTAACAT[A/G]CCATTCCACATTTCT | 115677 |
rs776661628 | snp | C/G | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863974 | GCAGTACAGTGGTGT[C/G]ATCTTAGCTCACTGC | 115677 |
rs776674502 | snp | A/C | 0.000288976 | 0.0120168 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818144 | ATGAGAAGGGCTTAG[A/C]TCTATTTTATTATTT | 115677 |
rs776690556 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805585 | GACAAGTAACAAGCT[G/T]TAGCCAAATTTTTGC | 115677 |
rs776698855 | snp | A/C | 1.65718e-05 | 0.00287848 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864935 | TATGTGGAGGAGTTA[A/C]CTTCAAATGCTGGCA | 115677 |
rs776708503 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846173 | TGTATGCCATATTTT[A/G]TGTATGTTTATGGCA | 115677 |
rs776729450 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817734 | CCCAAACTAGACCCT[C/T]AAGAAGGGCATCATT | 115677 |
rs776736950 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825876 | TTCTTTAGGCATCAG[C/T]CATAATAACAAATGG | 115677 |
rs776762076 | snp | A/G | 1.65957e-05 | 0.00288055 | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168824638 | TTTTCTAACAGGGCA[A/G]ACCTGGAAATTAGCT | 115677 |
rs776769372 | snp | A/G | 1.66101e-05 | 0.0028818 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828489 | AAATGTACAAGAGAA[A/G]AAGAGAAAATCAGTG | 115677 |
rs776814055 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802085 | GGTATTTGAGAACTG[A/G]GTAACAGAGATGGTG | 115677 |
rs776846242 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799519 | CTACCTGAGCCTCAG[-/T]GGCTGAAGACAACTT | 115677 |
rs776921179 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809877 | GAGGATTATTTTTCC[G/T]TCATGAGAGAGGCTA | 115677 |
rs776927142 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854188 | ATATAAAGACACTTT[A/T]GTAATGTGCAATGAA | 115677 |
rs776939975 | snp | A/T | 1.97244e-05 | 0.00314036 | utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802639 | ACAAAAGCCAGACAC[A/T]TTTCAACATGAGGGA | 115677 |
rs776953846 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790810 | CTGCTTTTGATGGTT[A/G]TATTTTGGTTTTGTT | 115677 |
rs776981963 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853223 | TAGTATTTTCTTGAC[A/G]TCTTTAAGGCAAAGC | 115677 |
rs777039070 | snp | A/G | 1.66754e-05 | 0.00288746 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851357 | ATGGAAGAAACTGCA[A/G]TTTTATCTACAGAAA | 115677 |
rs777140156 | snp | A/G | 4.33633e-05 | 0.00465615 | intron-variant, synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850913 | TGATTTAAGATACCA[A/G]GACACATTCCTTCCT | 115677 |
rs777176277 | snp | A/G | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863805 | ACACCAGCATGTGAA[A/G]CCCTCAAAGTACGGA | 115677 |
rs777210604 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789817 | CAGACCGAGAAACAA[A/C]GGGCCTTCAAGAAGC | 115677 |
rs777224752 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819999 | GGCTGCTGTGAATTG[A/G]GACTCCAGCTATTCA | 115677 |
rs777228397 | snp | C/G | 3.31356e-05 | 0.00407022 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861960 | CTTTATCTATTTCAG[C/G]CCCTGGTGCAGCCCA | 115677 |
rs777279144 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791561 | AGATCCCTGAGGAAT[C/T]GCCACACTGTCTTCC | 115677 |
rs777305972 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833979 | CTTGAGGGTACCCGA[C/T]ATAATGAAAAAGTAT | 115677 |
rs777318269 | snp | A/G | 1.65872e-05 | 0.00287981 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862048 | GTTGAATTTGGAAAA[A/G]GGTAAGAATCATTCT | 115677 |
rs777321063 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789399 | CTTACGTGGCTGCAG[C/G]CAAGAGGGCTTGTAT | 115677 |
rs777336156 | snp | A/G | 0.000116184 | 0.00762091 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859651 | AGGTAACATTTAAGG[A/G]GACTGGTTGTAATTT | 115677 |
rs777362695 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839444 | TAGAGAGGGAGCCTG[G/T]CTTGTTCCATTTTCT | 115677 |
rs777392947 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845372 | TCTTCCAGGCACCCA[C/T]CCTTCAAGGGCTATG | 115677 |
rs777428628 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817971 | ATGAAGTTTGGATAG[-/A]AAAATATCAGCACAT | 115677 |
rs777443853 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844603 | AAGATTCAGCCTGGG[C/T]GGCACGCCTGTAATC | 115677 |
rs777444835 | snp | C/T | 1.65652e-05 | 0.0028779 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859547 | TTTGGAAGCGAACTC[C/T]TACAAACTGTCATCA | 115677 |
rs777493196 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808943 | AGAAAGCAGAAGCAA[A/G]GTGTTAAAATCTCTA | 115677 |
rs777544043 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820267 | GTGACTGACCCAACT[A/C]TCTGTGCCTTGGTGT | 115677 |
rs777593240 | snp | A/C | 1.65734e-05 | 0.00287862 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828253 | GGCCTTTCTCCAACT[A/C]CAAAGGGAATCAAAT | 115677 |
rs777607057 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850474 | CTGTCATTCTCTTCC[C/G]TGCAGACTAGCAGAA | 115677 |
rs777619156 | snp | A/G | 4.9894e-05 | 0.00499445 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851322 | GCAAGATTGACATTG[A/G]AAAAGATATCCAGGC | 115677 |
rs777653810 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853688 | AGGTGTCTTAGCAGT[G/T]TAGTCAGAGTTTACT | 115677 |
rs777656773 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849209 | ACCCACCAACTTCTC[C/T]AAAGCCTTGTTCATG | 115677 |
rs777693112 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811469 | TTATAATGACAGTCA[C/T]AGTTATAGTAGTTTT | 115677 |
rs777707351 | snp | C/T | 0.000129847 | 0.00805647 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855319 | AACTCTTACTTCTTC[C/T]CCCTTGTTAGACATC | 115677 |
rs777713540 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833503 | CAGCCTACTTCCTGA[A/G]CAGGCTAAATCCAAC | 115677 |
rs777771183 | snp | A/G | 2.02612e-05 | 0.00318279 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802602 | ATTACAGTGTCCAGA[A/G]TGCTGGAGCGTAGGT | 115677 |
rs777905105 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812826 | TCCCTTTGTTTTAAC[C/T]TTTTTTAAACTCAAC | 115677 |
rs777955889 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847085 | TAAGTGAATAAACAC[A/G]CCTGCACCATGGATG | 115677 |
rs777973219 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805483 | CAAGAAAGGCGAAGT[A/G]AGATCCAATTATCTC | 115677 |
rs777982217 | snp | C/T | 1.65976e-05 | 0.00288072 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864979 | GGCATAAAACAAGAC[C/T]CTGAACATACTACCT | 115677 |
rs778014546 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838404 | GCCATCACATCTGGC[C/T]AATTTTTGTATTTTT | 115677 |
rs778056340 | in-del | -/GCCTGG | 1.65682e-05 | 0.00287817 | cds-indel, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828170 | AGTTGTGTTAGCAGT[-/GCCTGG]GCCTGGGCCTGGGCC | 115677 |
rs778077846 | snp | C/G | 3.37712e-05 | 0.00410907 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856647 | TGGCTGTGTCCCACT[C/G]AGACAGTGTGAAAGG | 115677 |
rs778107084 | in-del | -/AGT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820388 | GCCTGGCACGTTGTA[-/AGT]AGTGCCCAGTAAGTG | 115677 |
rs778163668 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829479 | GTGCCTGCCACCACG[C/G]CTGGCTAATTTTTGT | 115677 |
rs778192785 | snp | A/C | 2.03913e-05 | 0.003193 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811648 | ACATCTGTTCTTCAG[A/C]AAAGGTACAAAATGC | 115677 |
rs778271922 | snp | G/T | 1.68957e-05 | 0.00290647 | splice-donor-variant | NOSTRIN | GRCh38.p7 | 2:168855461 | CAAAAGACAAGGAAG[G/T]TGTGTAACCATCTCT | 115677 |
rs778281520 | snp | C/T | 1.66029e-05 | 0.00288117 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851065 | TGGCTGATCTTACCC[C/T]AATTTTCATTCTTTT | 115677 |
rs778283098 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833811 | AGAACATCTTAAAAC[-/A]ATCTCAAATCGTGGC | 115677 |
rs778312279 | in-del | -/A | 0.0017355 | 0.0294064 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851419 | GTGAGTATGAAATGG[-/A]AAAAAAAAAGTTACA | 115677 |
rs778318586 | snp | A/C | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845501 | TAGCTTGCCTTCTTC[A/C]ATATATGTTAGGGAA | 115677 |
rs778337072 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850596 | TGGAATTCTTCCCAA[-/T]TTTTTTTTTTTTTTT | 115677 |
rs778341885 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835494 | GGTGGCAGCATCAGC[C/T]TGGACATTTTGCTGT | 115677 |
rs778359462 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858338 | TTCATTACGCATGCT[-/C]TGCATCTGGGTAGAC | 115677 |
rs778381652 | snp | A/G | 1.65666e-05 | 0.00287802 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864893 | TTTGGATCTTTGAAT[A/G]GGAAAAAAGGCCATT | 115677 |
rs778405014 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823312 | TGAGCCACCGCGCCC[A/G]GCCAGTTGCATTAGT | 115677 |
rs778409963 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833552 | GCATAATTTATCTCT[A/G]GAGCATCATCTTCAG | 115677 |
rs778462603 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820503 | ACCACTGTCTGGACA[A/G]TCTCTTTAGGTGCAA | 115677 |
rs778464938 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168846962 | AAAAGGTAATTTCCT[A/T]TCTATAAAAGTGTCT | 115677 |
rs778505647 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833313 | GGAGGTGGAGAAAGA[A/G]GGCCATGAGCTTATT | 115677 |
rs778506174 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827709 | AGTAGCTAGGACTAT[A/G]GGCGTGCATCACCAC | 115677 |
rs778541027 | snp | C/T | 1.88891e-05 | 0.00307314 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824756 | GCAAAATCAACCCTT[C/T]TTTTATTTGTTTTTT | 115677 |
rs778557583 | snp | C/G | 1.80331e-05 | 0.00300271 | intron-variant, synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850937 | CCTTCCTGGAAATCT[C/G]CCTCCACTATGGTTT | 115677 |
rs778563071 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785664 | TTGTGAGGAGTATGA[A/G]GAAGTCAGGGGCAAA | 115677 |
rs778619401 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790268 | ATAAAATGGGAAACT[A/G]TGAGTTCATATGATA | 115677 |
rs778627556 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865115 | AGCACTTTGCATTCA[C/T]GATTATTAGCTTGAA | 115677 |
rs778657144 | snp | C/T | 5.01157e-05 | 0.00500553 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855434 | GACTGCAGAGAGACA[C/T]TGAAAAAGCCTCAAA | 115677 |
rs778668695 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803593 | ATGGTTGGAAAAAAT[A/G]GAACTATAGTTACTA | 115677 |
rs778672376 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789670 | AGGGTATGAAGTGGA[A/G]GTGCGGTTAATTGGG | 115677 |
rs778729955 | snp | A/G | 3.31406e-05 | 0.00407053 | | | GRCh38.p7 | 2:168851087 | CATTCTTTTCAGAGC[A/G]TTCTGGAGCTGGAGA | 115677 |
rs778756017 | snp | A/C | | | | | GRCh38.p7 | 2:168799708 | TCTCTTCCTAACGCC[A/C]GTCTGCTGAGGTTCA | 115677 |
rs778787172 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842508 | AGTAAAAGTAAAATA[A/G]TATCGCTAGATAGGA | 115677 |
rs778826394 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809249 | TGATCTTAATGCATT[A/G]TGTCCAATCTCAATA | 115677 |
rs778835916 | snp | A/C | 3.332e-05 | 0.00408153 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859681 | TCTTGATTGGGCCTG[A/C]TGGGTGGAGTGGCTT | 115677 |
rs778850946 | snp | A/T | 3.32978e-05 | 0.00408017 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831467 | CCTTTTTCCTTTTTC[A/T]ATAGCTTGACAATGA | 115677 |
rs778947014 | snp | C/T | 1.65638e-05 | 0.00287778 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862009 | CAAGGCCTTGTATTC[C/T]TTTCAAGCCAGGCAA | 115677 |
rs778987348 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818272 | ACTCCTCTCGCCTCA[A/G]CCTCTCAAGTAGCTA | 115677 |
rs779014023 | in-del | -/TG/TGTG/TGTTTA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849921 | AACATTTTCTCATTT[-/TG/TGTG/TGTTTA]TTTTTTTTTTTTTGA | 115677 |
rs779046467 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791842 | TGGGGTTGTTCTTTT[C/G]TTGTAAATTTGTTTG | 115677 |
rs779090989 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794653 | ACCACGCCCAGCCCA[A/G]CGGATGATTTTTAAC | 115677 |
rs779130553 | in-del | -/GA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819950 | GCACAGATGCCTTTG[-/GA]ACAGGCCTGGAAGCT | 115677 |
rs779149310 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806250 | TGGTTTCTTTAACAC[C/T]GTGAGGATCATCACT | 115677 |
rs779151642 | snp | C/T | 1.65789e-05 | 0.0028791 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861935 | TGCTAACACAGCATA[C/T]TAATTACAGCTTTAT | 115677 |
rs779207757 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859390 | ATTTTCTGTGAATAT[C/T]TGTATGAGTTAAATG | 115677 |
rs779234837 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819256 | TCTAAGTGGGGTGTG[A/C]CTTGCTGCCTCTGCC | 115677 |
rs779239409 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862348 | ACTGATACACAGGAA[A/G]GTTAGGTGCTTTGGC | 115677 |
rs779290737 | in-del | -/CAAA | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857018 | TAAAATAGTATTCTC[-/CAAA]CAGAGTCGTTCTTTA | 115677 |
rs779311720 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824240 | TCTCCTTCTTGCATA[C/T]ATGTGTGCATGTGTG | 115677 |
rs779402579 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815568 | AATAAAAGAAGGAGG[A/T]ATAGTTGACCACTTG | 115677 |
rs779444549 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825616 | CTGAAAGGTATTGGT[C/T]CACATTCTTTTCAAT | 115677 |
rs779475008 | in-del | -/TGTGGAGGAGTTACCTTCAAAT | 1.65679e-05 | 0.00287814 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864921 | TTTTCCTGCCGCTTA[-/TGTGGAGGAGTTACCTTCAAAT]TGTGGAGGAGTTACC | 115677 |
rs779508505 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792714 | TGAACTCCTGACCTC[A/C]GGTGATCCACCTGCC | 115677 |
rs779555209 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854901 | TTTTAGCTCACATCT[C/T]CCCAGTACTGAGCCA | 115677 |
rs779562546 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857495 | CAGGGAGGTGGGCCT[C/T]CTGGCCTTTGTGCTG | 115677 |
rs779594614 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835261 | TTTTTGCATTTTTAG[C/T]AGAGGCGAGGTGTCA | 115677 |
rs779607429 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811091 | GGACAAAGTTTTCTT[A/G]CCAGGTTATTTACTG | 115677 |
rs779670432 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833508 | TACTTCCTGAACAGG[C/T]TAAATCCAACTTAAA | 115677 |
rs779681317 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865104 | CTGCATGTCACAGCA[C/T]TTTGCATTCATGATT | 115677 |
rs779788109 | snp | A/G | 8.28974e-05 | 0.00643753 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851213 | CTCTCCATTTCTGGT[A/G]TGCCTGGTAAGAAGG | 115677 |
rs779788188 | snp | A/G | 1.6636e-05 | 0.00288405 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824618 | ACATCCTATTTAACT[A/G]GTCCTTTTCTAACAG | 115677 |
rs779830061 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844256 | TGCCAGAAACAGCCA[C/T]GCAGCTTATGCACGG | 115677 |
rs779878208 | snp | C/T | 3.31873e-05 | 0.0040734 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828124 | CCTAGGAAAATGACA[C/T]TCACCTTTGTTCCCC | 115677 |
rs779886702 | snp | A/G | 1.67237e-05 | 0.00289164 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860960 | CTACTGGCAGGGCAC[A/G]TTGCTACATTTAAAT | 115677 |
rs779897280 | snp | C/G | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860839 | TCGGCCTTTTTTAAT[C/G]AAGAGATTAGAGAAT | 115677 |
rs779898995 | in-del | -/TTC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849171 | GAGACATACCCATCT[-/TTC]TTCTTCCCTATGGTC | 115677 |
rs779930739 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799759 | GATTGGGGAGAGGGA[A/G]AGAAAGACATATACC | 115677 |
rs779979957 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798423 | CAATATTTGTTTGTG[A/C]ATACTTCATAAATGC | 115677 |
rs779984151 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851104 | TCTGGAGCTGGAGAA[A/G]GAAAGAATTCAACTT | 115677 |
rs780061821 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830820 | GTTGAGGTTTTTGCT[G/T]CATGGATTGACGTGG | 115677 |
rs780096877 | snp | C/T | 1.6569e-05 | 0.00287824 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168862030 | AGCCAGGCAAGATGA[C/T]GAGTTGAATTTGGAA | 115677 |
rs780177942 | snp | C/T | 1.73679e-05 | 0.0029468 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855345 | ACATCCTTCTTTTTT[C/T]CTAAAGGAAGAAGAT | 115677 |
rs780182316 | in-del | -/TTGAG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791978 | GCTGTGCAGAAGCTC[-/TTGAG]TTTAATTAGATCCCA | 115677 |
rs780271657 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804908 | TCAGAAATTTTATGA[C/T]AACATTACAGTTGTT | 115677 |
rs780279739 | snp | A/G | 1.65985e-05 | 0.00288079 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168843028 | TCAACTGAAAAGTTG[A/G]AAAAGGAAGATGAAA | 115677 |
rs780318191 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796622 | ATTCTCAGTCCCAAG[A/T]CTCTCCTTACCTCAT | 115677 |
rs780371161 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808730 | AAATGCAAAAACTTA[A/C]TATGTCCTTGGATAG | 115677 |
rs780379953 | snp | C/T | 8.08963e-05 | 0.00635937 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802611 | TCCAGAATGCTGGAG[C/T]GTAGGTGAAAGGACA | 115677 |
rs780385514 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795890 | TTAAAGTACTCATAA[A/G]TGCTTCTAAGTTGGA | 115677 |
rs780431686 | snp | A/G | 4.0286e-05 | 0.00448792 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168802614 | AGAATGCTGGAGCGT[A/G]GGTGAAAGGACAAAA | 115677 |
rs780432901 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815783 | CATATATATCACAGT[A/G]TATTGGACATCTCCA | 115677 |
rs780440631 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807628 | TCTCAACTTGCATGT[C/G]CCTGGGCATACTGGC | 115677 |
rs780450733 | in-del | -/CT | 1.65946e-05 | 0.00288046 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864977 | AGGCATAAAACAAGA[-/CT]CTCTGAACATACTAC | 115677 |
rs780452268 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840845 | CTGGGGAGCTATAGT[C/T]AAAACTCAGATTTTC | 115677 |
rs780456316 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863186 | TAAATGAAACACGAC[A/G]TTGGAGCCTTAGGGA | 115677 |
rs780495640 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847893 | TCATTTTAATGATTT[A/C]CCTGAAATGTAATTA | 115677 |
rs780529076 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849838 | TCTCTAAGAATGCTT[A/T]GTTGCTAAAGCTTTC | 115677 |
rs780550379 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827035 | GCAGAAAATCTGGCA[C/T]CTTTTGGTCTAGTTC | 115677 |
rs780555701 | snp | C/T | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859532 | TTTGAAACTAGACCT[C/T]TTGGAAGCGAACTCC | 115677 |
rs780589119 | snp | A/C/T | 4.97074e-05 | 0.00498514 | missense, synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859524 | CAGAACAATTTGAAA[A/C/T]TAGACCTTTTGGAAG | 115677 |
rs780613691 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844421 | TTTAAAGCAGATACA[A/G]TTGGAGAAAGCCATG | 115677 |
rs780618478 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808195 | CTACTCATTTCTACA[C/T]TGGTTATGAGCAGAG | 115677 |
rs780620147 | in-del | -/T | 0.000488092 | 0.0156143 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828142 | ACCTTTGTTCCCCAC[-/T]TTTTTTTGCCTTTAG | 115677 |
rs780631137 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800124 | CCAGCTGATGAAATA[C/T]GGCCTCAGCCAACAG | 115677 |
rs780631677 | snp | A/G | 1.81774e-05 | 0.00301469 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834361 | GGGCGCATGTGCCAT[A/G]GAGAGGGATGGACTT | 115677 |
rs780690121 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847040 | TTAAAGGCAGCAAAC[A/G]TCCCAAATGTCCAAC | 115677 |
rs780706209 | snp | G/T | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801356 | CTCTTGAGTAGCTGG[G/T]ACTACAGGCACATAC | 115677 |
rs780742958 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858700 | TTCCTCCAACGATTA[A/G]AGACTTTCTCCATCA | 115677 |
rs780757560 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803837 | TCCATTGTTAATTGT[C/G]AATAATTTTTAAGAA | 115677 |
rs780768592 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851686 | GACATGTTTCAATGA[C/T]CTATAATTAATCACT | 115677 |
rs780808030 | snp | C/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856159 | TGGAAAAATAACAAT[C/G]AAGATGCTTTAAGCA | 115677 |
rs780817769 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813834 | TGCTACATATTAGGT[A/C]ATTTATGTAATAAAT | 115677 |
rs780845835 | snp | C/T | 8.29552e-05 | 0.00643978 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828129 | GAAAATGACACTCAC[C/T]TTTGTTCCCCACTTT | 115677 |
rs780850965 | in-del | -/AGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788929 | GATAGATAGATAGAT[-/AGA]TAGATGATAGATATT | 115677 |
rs780859391 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855075 | ATCAAGAAAATGAAA[A/T]AGCTATAGCAAGGGT | 115677 |
rs780865187 | snp | A/G | 9.9425e-05 | 0.00705001 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856766 | GAAAGACACAGCAGC[A/G]TTAATGGATGAGGTA | 115677 |
rs780883459 | in-del | -/AG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807283 | TACACACACACACAG[-/AG]AGAGAGAGAGAACTA | 115677 |
rs780890114 | in-del | -/TTTAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862671 | TTTGTGTCACAGAGT[-/TTTAC]TTTACTTAACATGGA | 115677 |
rs780984706 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862403 | AAGATTTGAACTTGG[A/G]AACACAGTCATGCTC | 115677 |
rs781000922 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823296 | GCTAGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 115677 |
rs781010553 | in-del | -/TC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842578 | GTATGATTCCACAAG[-/TC]TCTACCTAACCTGGT | 115677 |
rs781012090 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813014 | AGTCAAAAAGAGAAA[-/C]CATTTTAAATATGAA | 115677 |
rs781116540 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849332 | TGCCCAGGCCTTGTA[-/T]TTTTTTCTTTCTTTC | 115677 |
rs781128951 | snp | A/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845273 | CCTCATCACTTCCTG[A/T]TGAAGCCGTGGTCTT | 115677 |
rs781159291 | snp | A/G/T | 3.3127e-05 | 0.00406972 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168861998 | AGCAGACTTTGCAAG[A/G/T]CCTTGTATTCTTTTC | 115677 |
rs781176220 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799568 | CTGCCTCCTCACAAC[C/T]CATATCCAGGAGAGG | 115677 |
rs781200486 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168801178 | AGTGTGTGGAAAAGA[A/C]CCCTCCTCTCCACTC | 115677 |
rs781208474 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830853 | GATGATGTGATGGGA[C/G]TAGCAACAATATCAG | 115677 |
rs781232457 | snp | C/T | 6.74047e-05 | 0.00580498 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855360 | CCTAAAGGAAGAAGA[C/T]CCTAACAGTGCAATG | 115677 |
rs781244619 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858906 | CAAGGTAATTATAAA[G/T]TTTCTAGTTCAAGGT | 115677 |
rs781282556 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797199 | AGCTCAGGTGATCCT[C/G]CCACCTCAGCCTCCT | 115677 |
rs781328237 | snp | A/C | 1.66098e-05 | 0.00288177 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168831483 | ATAGCTTGACAATGA[A/C]GTTGAAAAGACAGCA | 115677 |
rs781443343 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824265 | TGTGTGCATCTGTGT[A/G]TATGTTTGGTTTGCT | 115677 |
rs781480844 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856840 | TTATTTTTAGAATAC[C/T]TGTTTCTGGTCCACT | 115677 |
rs781500528 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842986 | GACATTGATGTTTTA[C/T]ATTAGCTCCTCAATA | 115677 |
rs781506508 | snp | C/T | 1.92591e-05 | 0.00310309 | stop-gained, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811627 | GAGAATTTCTGCAAA[C/T]AGGTCACATCTGTTC | 115677 |
rs781524476 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794542 | GTTTTTACTAGAGAC[A/G]GGGTTTCACTGTGTT | 115677 |
rs781567248 | in-del | -/AAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839884 | GAGAGACTCCGTCTC[-/AAAAA]AAAAAAAAAAAAAAA | 115677 |
rs781573628 | snp | A/C/G | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865216 | AAATTCTAGGAGACC[A/C/G]TAGAGATGATCCAGT | 115677 |
rs781575138 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855312 | GAATAGCAACTCTTA[A/C]TTCTTCCCCCTTGTT | 115677 |
rs781577319 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796688 | AGTTCTCTAAGTGGC[C/G]CCTTGGGATTCTTGC | 115677 |
rs781578798 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848023 | CCCACTAGGGATGCA[A/G]TATGTTCTAAAACCT | 115677 |
rs781626428 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805030 | TAATATCATAATTTT[A/T]AAAATACATTCTAAA | 115677 |
rs781665518 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804271 | CATGCTGAATAGTTC[C/T]TTGTGCTATGCTGGG | 115677 |
rs781683392 | snp | A/G | 3.32088e-05 | 0.00407471 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850873 | ATGCCTTTTGGGTCA[A/G]AAGAGCCTGGGGAAA | 115677 |
rs781699436 | snp | C/T | 3.31549e-05 | 0.0040714 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864835 | CTGTATTTTCACAGG[C/T]GACATTGTGATTATA | 115677 |
rs781707455 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849035 | CAACACAGGGATATA[C/G]AGGAATACCATACTG | 115677 |
rs781715247 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807131 | CAAACTGTGCTCCAT[A/G]GAACCCTTTCAGAGT | 115677 |
rs781730407 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822446 | TTTGCTCAGTCTATG[C/T]CACGGAGTTAATTTG | 115677 |
rs781734007 | snp | A/G | 2.064e-05 | 0.00321241 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802715 | CCTGCGTGTGAGGAG[A/G]GTGGAGGGTGGATTT | 115677 |
rs796124430 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849636 | GCTGGGATTATAGGC[A/G]TGAGCCACCGCACCT | 115677 |
rs796132864 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840203 | CAAGCTTGAGTTTCT[A/G]CAGACACATGTGGTT | 115677 |
rs796146044 | snp | A/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800681 | TTATGGAAACTGGCA[A/G]GGGAGGCCAATTTCC | 115677 |
rs796166866 | in-del | -/TG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850615 | TTTTTTTTTTTTTTT[-/TG]TAAAAACAAGGCCTG | 115677 |
rs796194578 | in-del | -/AAAC | | | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865128 | ATGATTATTAGCTTG[-/AAAC]AAACAGTCAGAAAAA | 115677 |
rs796224801 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855636 | AGAAGAAAAAAGAAA[A/G]CCAAAAAAAAAAAAA | 115677 |
rs796271865 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791755 | CAGTGACGGTTTTTT[-/T]CATGTGTTTTTTGGC | 115677 |
rs796343255 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792993 | ACTTTTGACTTTTCA[A/G]CACTCCAAAGCCTAT | 115677 |
rs796348221 | in-del | -/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864296 | TCCTGTTTTTTTTTT[-/T]CTGAGACAGAGTCTT | 115677 |
rs796392667 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859366 | TCCTCCATTTTTTTT[-/T]CCTTCGGCATTTTCT | 115677 |
rs796441506 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797690 | AATTTTTTTTTTTTT[-/T]AATGTTGCTTGGTGT | 115677 |
rs796448347 | in-del | -/CTTA | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864634 | TCAGTTGTTCATTAT[-/CTTA]CTTACTCTTTTTAGT | 115677 |
rs796490860 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786754 | TCCTGCCCTAAAACC[-/T]TTTAGTAAACTTTCA | 115677 |
rs796627574 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854365 | GAAGCCTGCATCCTC[C/G]CCTCCCACCTTGAGT | 115677 |
rs796661825 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860434 | CCAGAACTTTGGGAG[A/G]CCAAGGCAGGCGGAT | 115677 |
rs796674324 | snp | C/T | | | intron-variant, missense, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863401 | TGCTGAGGAAAAGAG[C/T]GAAAGGAAGACTGAA | 115677 |
rs796695688 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853898 | TTTGAGACGGAGTCT[C/T]GCTCTGTGGCCCAGG | 115677 |
rs796719812 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858073 | ACATTTTCTGTGACC[A/G]CACAAGCTGTTTAGT | 115677 |
rs796741057 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845414 | TCACCTCAGTGTCTC[C/T]ATCCTCATCACCCTT | 115677 |
rs796779568 | in-del | -/AAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855639 | AGAAAAAAGAAAGCC[-/AAAA]AAAAAAAAAAAAGGA | 115677 |
rs796841369 | in-del | AA/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840540 | TCTCAAAAAAAAAAA[AA/C]AAAAAAAAACAAAAA | 115677 |
rs796847411 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864509 | CAGGCTGGTCTCGAA[-/A]CTCCTGACCTTGTGA | 115677 |
rs796888982 | in-del | ACA/GCGCG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834503 | GTGCGCGCGCGCGCG[ACA/GCGCG]ACACACACACACACA | 115677 |
rs796954636 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836683 | AGTATCTTGCCTCCT[A/G]CCTCACAGAGTAAAT | 115677 |
rs797000709 | snp | C/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801586 | GGAGGCTGAGTCAGC[C/G]AGTCAGGTGAAAACT | 115677 |