SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3931 | snp | C/T | 0.395298 | 0.203442 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864871 | AGATCCAAACCACCA[C/T]CCTCCTTCTTTTTTC | 115677 |
rs10181 | snp | A/C/T | 1.65718e-05 | 0.00287848 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864937 | GTTGCCAGCATTTGA[A/C/T]GGTAACTCCTCCACA | 115677 |
rs471087 | snp | G/T | 0.41023 | 0.191902 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845128 | TTGAACATAAGCTCC[G/T]GGTACTCTCTTGGTT | 115677 |
rs472233 | snp | C/T | 0.433818 | 0.169443 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832237 | AGATCGTAATTCCTC[C/T]TAGAATGTATTCCCT | 115677 |
rs474538 | snp | A/G | 0.440057 | 0.162414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838686 | CTATCTATTCCCCAT[A/G]TACAAGCCAAGCTGA | 115677 |
rs474751 | snp | A/G | 0.436408 | 0.16659 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845527 | GGGAAGGCTATGATT[A/G]TCTTCATTATCAGAA | 115677 |
rs475808 | snp | C/G | 0.382473 | 0.212016 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819056 | GGAAAGAAAAAAATG[C/G]AAAAGGGCTAGAGAA | 115677 |
rs479661 | snp | C/T | 0.16846 | 0.236329 | missense, downstream-variant-500B, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864867 | CCAAACCACCATCCT[C/T]CTTCTTTTTTCTCGT | 115677 |
rs481067 | snp | A/C | 0.495818 | 0.0455352 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835859 | ATTTTGTTCCTGTAC[A/C]CCAATATTATTCGTG | 115677 |
rs482435 | snp | A/G | 0.391024 | 0.206427 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819535 | GTTGAGATAAAAGCC[A/G]TTCAGCGCTAGAGGC | 115677 |
rs486153 | snp | A/G | 0.471958 | 0.115042 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826456 | AGGAAGCAAGGGAGG[A/G]AGGGAGGGAAGAGAA | 115677 |
rs486838 | snp | A/G | 0.368529 | 0.220116 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826446 | GGAGGAAGGGAGGGA[A/G]GAGAAAGAAAGGAAA | 115677 |
rs487756 | snp | C/T | 0.391024 | 0.206427 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830049 | CTCTATTCAGAGTTT[C/T]GGGTGATGGACAGAA | 115677 |
rs488621 | snp | A/G | 0.500003 | 0.00218935 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851042 | TGACTTCCATTTTGC[A/G]TAACAACTGGCTGAT | 115677 |
rs490278 | snp | A/G | 0.478603 | 0.101197 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814693 | CATAATTCAAGATAC[A/G]GTGAAGGAGGACATG | 115677 |
rs494120 | snp | A/G | 0.095934 | 0.196885 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814219 | TGACCTCAGAATCAC[A/G]TCACTGTGTGGGAGA | 115677 |
rs495074 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830831 | TGCTGCATGGATTGA[C/T]GTGGAAGATGATGTG | 115677 |
rs495135 | snp | A/G | 0.453087 | 0.145793 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830849 | GGAAGATGATGTGAT[A/G]GGACTAGCAACAATA | 115677 |
rs497808 | snp | A/C | 0.479014 | 0.100263 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848527 | CACTGCTTGCAAATG[A/C]AAGTAGTAAAAGGCT | 115677 |
rs498231 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810985 | GTTATAAATTTATTA[A/G]TTACCCTTTATAAAT | 115677 |
rs498488 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820374 | ttacaacgtgccagg[C/T]gtcattctgggtgtt | 115677 |
rs501303 | snp | C/T | 0.411242 | 0.191052 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840918 | GAATTCTGGAATTTG[C/T]AATTTTTACAAGCAT | 115677 |
rs503664 | snp | C/G | 0.479014 | 0.100263 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833166 | CTATAATAATTTTCT[C/G]CCCAGTTACAATTCA | 115677 |
rs505283 | snp | A/G | 0.496714 | 0.0404017 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846524 | TAAGTAATGAAACCA[A/G]TTCCACAAACCACAT | 115677 |
rs506362 | snp | G/T | 0.470521 | 0.117772 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864530 | tgggaggccaaggtg[G/T]gtggatcacaaggtc | 115677 |
rs508423 | snp | C/T | 0.410399 | 0.191761 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844544 | TTCCAGCCTCAATGT[C/T]CTCATAATGTCATGA | 115677 |
rs511013 | snp | C/T | 0.285257 | 0.247501 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827417 | CCTGTTCATGTCCTG[C/T]TGCTGCTCTTGGGGT | 115677 |
rs514629 | snp | C/T | 0.258288 | 0.249863 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808611 | CACAGTATTAAGCTA[C/T]GGATTTTTATGTATT | 115677 |
rs518337 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842840 | TTTTTTTCTTATAAA[A/G]ATCTTTCATTTTGTC | 115677 |
rs519345 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860346 | ACACAGTAGGGCTTA[A/G]AAATCTTTGAATTAT | 115677 |
rs519599 | snp | C/T | 0.15698 | 0.23205 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831170 | CACACAGCTAATGTG[C/T]GGGTGCCTTGCTCTT | 115677 |
rs522893 | snp | A/G | 0.489689 | 0.0710578 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834219 | TTCTTGGCCTAGAGT[A/G]AAAAACATACAAACA | 115677 |
rs526418 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838603 | ATCCTCTCTCAGGCC[A/G]CAATCATCTTTTGCT | 115677 |
rs527393 | snp | A/G | 0.497151 | 0.037632 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853247 | GCAAAGCACCCCAAT[A/G]TCTGACTTTATAGTC | 115677 |
rs529002 | snp | A/C | 0.404035 | 0.196909 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847386 | AGGTCTAGGGAGGTG[A/C]TCAGGAATCTGACTT | 115677 |
rs531328 | snp | G/T | 0.4862 | 0.0819127 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844328 | TCTCCAGAATTGATA[G/T]TTATTTAATTTGGTC | 115677 |
rs531864 | snp | C/T | 0.491104 | 0.0660973 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847150 | TAATGGCACGGGAAA[C/T]TGTTCACATGTACGG | 115677 |
rs532779 | snp | A/T | 0.483272 | 0.0899109 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847241 | TCATACATATACACA[A/T]ACCTAGACTGAAATA | 115677 |
rs533492 | snp | A/G | 0.158962 | 0.232835 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863296 | TTAGAGACCGAGAAT[A/G]ATGTCCTTTAAGAAT | 115677 |
rs534310 | snp | C/T | 0.261884 | 0.249717 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863363 | AAAGGAGTTAATAAT[C/T]TCCTTTGTCTTAGAA | 115677 |
rs534771 | snp | A/C | 0.27278 | 0.24896 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863705 | ATGTCTCTGCATTAT[A/C]CCTGATTTCACAGGC | 115677 |
rs539400 | snp | C/G | 0.270351 | 0.24917 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863193 | GCCAGCTTCCCTAAG[C/G]CTCCAACGTCGTGTT | 115677 |
rs540652 | snp | C/T | 0.499437 | 0.016763 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850918 | TAAGATACCAAGACA[C/T]ATTCCTTCCTGGAAA | 115677 |
rs543262 | snp | C/T | 0.460702 | 0.134554 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807717 | TACCTCGCTCCCAGC[C/T]ATACTCTGCCAATTC | 115677 |
rs546146 | snp | C/G | 0.494855 | 0.0504572 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852687 | GATCAGGCAACAAGA[C/G]GGTAGAAGGCAGAGG | 115677 |
rs548367 | snp | C/T | 0.489318 | 0.0722982 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812952 | AAGTCTGTTTCAGCT[C/T]GCTCATATCTTTCTT | 115677 |
rs549582 | snp | A/G | 0.136847 | 0.222927 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833579 | TTTCCTAGTCTACAT[A/G]GTTGAATTTAACTGA | 115677 |
rs550081 | snp | A/G | 0.385359 | 0.210185 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822171 | GTCAATAAATATCTC[A/G]TCGCACTTAAAAATA | 115677 |
rs551037 | snp | A/G | 0.100231 | 0.200173 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813198 | GGCTTTCTAATCTGG[A/G]TAATGAGTTGAATTC | 115677 |
rs552445 | snp | C/G | 0.434687 | 0.168495 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833261 | GAAATGAGAGTGTGA[C/G]GCATGAATATTTGGT | 115677 |
rs553827 | snp | C/G | 0.0737376 | 0.17729 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168846972 | TACTTCCTCAAGACA[C/G]TTTTATAGAAAGGAA | 115677 |
rs557002 | snp | G/T | 0.485118 | 0.0849685 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825019 | gtaatcccagaactt[G/T]ggaaggccaaggcag | 115677 |
rs558922 | snp | C/T | 0.495521 | 0.0471118 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825239 | TGTAAACAGGGATAA[C/T]AAGACCTCTCAAGGG | 115677 |
rs559113 | snp | A/T | 0.499891 | 0.00738737 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846419 | CTCTGAAGGAATTTG[A/T]ACATCCAACCTGTAG | 115677 |
rs560952 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847977 | TTTGACAAGTGCTGA[A/G]CCACTAGCATCAATC | 115677 |
rs566465 | snp | A/T | 0.499609 | 0.0139722 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848594 | TATGCATACCATGGA[A/T]TATTATTCAGCCAAA | 115677 |
rs569821 | snp | A/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812295 | TCTCTTTAGAGTTGC[A/T]TATTACGGAGCTATC | 115677 |
rs569997 | snp | C/T | 0.498673 | 0.0257246 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858383 | CTGGTAGATTTTGTG[C/T]CACCCACGGAAGGTT | 115677 |
rs572411 | snp | A/G | 0.155656 | 0.231515 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829520 | AAGCCTGACCAACAT[A/G]GCGATCCCTGGTCTC | 115677 |
rs576062 | snp | C/T | 0.498693 | 0.0255257 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859176 | GTTGATTGTAGAAGG[C/T]AGATTTTTGGTGGTC | 115677 |
rs577192 | snp | C/T | 0.162253 | 0.234095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852594 | GGTGTCACTCTTCTC[C/T]GATATGGAGAACAAG | 115677 |
rs578521 | snp | C/T | 0.40595 | 0.195396 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837951 | cctgatctttatata[C/T]tgcagtttctgaaga | 115677 |
rs578797 | snp | A/C | 0.410399 | 0.191761 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844845 | ACTGCACACTAGCCT[A/C]GGCGACAGAGCAAGA | 115677 |
rs580507 | snp | A/G | 0.322959 | 0.239117 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862392 | TGTTTCCAAGTTCAA[A/G]TCTTGTGTTGCCACA | 115677 |
rs581363 | snp | C/T | 0.270351 | 0.24917 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862471 | AAAAGGTGGGGTACA[C/T]CTCTAATCACTTTCC | 115677 |
rs696805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816123 | CTGCCTCCATTCATC[C/T]CACTCAGCCATGTGC | 115677 |
rs700547 | snp | C/T | 0.0611083 | 0.163768 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801721 | TGGCCTATTGATGTA[C/T]GACAGCCATTTGCTA | 115677 |
rs700548 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827947 | TGCTTTTTTCCCAGT[C/T]ATTTTTCATTTAGAT | 115677 |
rs829950 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797545 | GTCCTTATAGCTTTA[C/T]GTTGGCCCAGCTGAC | 115677 |
rs829951 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790908 | AGGATTTTTTTCCTT[C/T]TGTCCTgaataagtt | 115677 |
rs829952 | snp | C/G | 0.0315505 | 0.12225 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786845 | agctactctggagga[C/G]gggggaggcagggaa | 115677 |
rs829955 | snp | C/T | 0.177503 | 0.239258 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805514 | ATACTTTCTTATGAT[C/T]GGATTCTTTCCCTTA | 115677 |
rs829956 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804951 | CATTTTGAAGTCAGG[G/T]TGAATGTAAATATTT | 115677 |
rs829957 | snp | A/C | 0.252702 | 0.249985 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802324 | ATGTCTCCAACAATT[A/C]TTGCGCTTGGTCTGA | 115677 |
rs829958 | snp | C/T | 0.230017 | 0.2492 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802273 | TCTCAGCCTGCAGTA[C/T]TAATCATGCTTTTTA | 115677 |
rs829959 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801338 | agctactcaagaggt[C/T]gaggcagaaggattt | 115677 |
rs829960 | snp | C/T | 0.102014 | 0.201495 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823569 | ttggacataaacaga[C/T]atgtacacagagaaa | 115677 |
rs830020 | snp | C/T | 0.499053 | 0.0217445 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829246 | gaaagaaagaaAAAC[C/T]GTTCTAGAAGGAAAG | 115677 |
rs830021 | snp | G/T | 0.412082 | 0.190341 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828762 | TTCTATTGCTTGAAT[G/T]TATCACAATTTATTT | 115677 |
rs830022 | snp | C/T | 0.0566069 | 0.158427 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823174 | aaaaaattagccagg[C/T]gtggtggctcacgcc | 115677 |
rs830023 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820011 | GCTCCTGGAGGCTGA[A/G]TAGCTGGAGTCCCAA | 115677 |
rs830024 | snp | C/G | 0.339341 | 0.233491 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818254 | AGGCGAGAGGAGTTC[C/G]CGAGCACAGGAGTCT | 115677 |
rs830025 | snp | A/T | 0.172834 | 0.237793 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818153 | AAAAACATAAAATAA[A/T]AAAATAGAGCTAAGC | 115677 |
rs830026 | snp | A/G | 0.188501 | 0.242318 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818145 | AAAATAATAAAATAG[A/G]GCTAAGCCCTTCTCA | 115677 |
rs830027 | snp | C/T | 0.443866 | 0.157848 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817869 | AAAGACATTTTCATA[C/T]TGAAGCTCTGTCATT | 115677 |
rs830028 | snp | A/G | 0.444533 | 0.157025 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817672 | AGGGAAAACGTAAGC[A/G]ATGGCAGCTCTAGAA | 115677 |
rs830029 | snp | C/T | 0.450734 | 0.149016 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817498 | AATTTTATGCAGAAT[C/T]CCACTGTATCATATA | 115677 |
rs830030 | snp | A/T | 0.4973 | 0.0366419 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817357 | CAAACCCCTTGAGCT[A/T]TAAGGTTTGAAAGCC | 115677 |
rs830031 | snp | A/G | 0.399968 | 0.200024 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812521 | atgggtatagcatgt[A/G]ttaataagtttctgc | 115677 |
rs830194 | snp | A/G | 0.442113 | 0.159977 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836132 | GTGAAGACTGACATG[A/G]AAAGAAATAAGAGTC | 115677 |
rs853666 | snp | A/G | 0.446641 | 0.154377 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817632 | CTAAAGTGTGCATTC[A/G]TTCCTAAGCTTAGTG | 115677 |
rs862637 | snp | C/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824761 | aaacaaacaaacaaa[C/T]aaaaaaaGGGTTGAT | 115677 |
rs862638 | snp | C/T | 0.450609 | 0.149185 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817383 | CTGAGGTAGCCCCTG[C/T]GGGCTCCCCACAAAC | 115677 |
rs865520 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849540 | tttgtatttttagta[A/G]agacggggttttgcc | 115677 |
rs1402835 | snp | C/T | 0 | 0 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834268 | TACAAGCTGGAAAAG[C/T]GCTTCATGTTTCTTG | 115677 |
rs1568550 | snp | A/G | 0.331411 | 0.236373 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821687 | CAACAGGAGCTGCTC[A/G]AACATCACTGCCTCA | 115677 |
rs2010230 | snp | A/C | 0.163236 | 0.234461 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801041 | AAAAGAAATTTAGGT[A/C]Aggcacagtggcaca | 115677 |
rs2010235 | snp | G/T | 0.384401 | 0.210799 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800921 | cccatctcttttttt[G/T]ttttttttttaaaag | 115677 |
rs2140046 | snp | C/T | 0.474182 | 0.110646 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849569 | CCACGTTGGGCAGGC[C/T]GGCCTTGAACTCCTG | 115677 |
rs2177076 | snp | A/C | 0.427119 | 0.176434 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841869 | cttaggtttaacaaa[A/C]tacggacatccatgt | 115677 |
rs2276666 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803071 | ATAAAGTGAGGGAGG[A/G]GAGTTTTTGTGCCTT | 115677 |
rs2276667 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845793 | CAAAAAAAAAAAAAA[A/G]AAGGAAGAAAAAAAC | 115677 |
rs2293130 | snp | A/G | 0.0191955 | 0.0960691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828123 | TCCTAGGAAAATGAC[A/G]CTCACCTTTGTTCCC | 115677 |
rs2433679 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817108 | GAGAAGTATGTACGC[C/T]GTGGGTTGTGAGATA | 115677 |
rs2433680 | snp | C/T | 0.14665 | 0.227637 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817066 | CAAGTATAAGACACA[C/T]TTAACACAGTGGCTG | 115677 |
rs2433681 | snp | C/T | 0.145978 | 0.227331 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816899 | CTTGATCTTCATTAA[C/T]GTTATGAGTGCCTTC | 115677 |
rs2461362 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817669 | GAAAACGTAAGCAAT[A/G]GCAGCTCTAGAACTT | 115677 |
rs2461363 | snp | G/T | 0.14665 | 0.227637 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817104 | AGTATGTACGCTGTG[G/T]GTTGTGAGATAATTA | 115677 |
rs2461385 | snp | C/T | 0.137187 | 0.223099 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843953 | TACGCAATCTTCATA[C/T]CCATCAAGAGAAGAA | 115677 |
rs2461386 | snp | C/G | 0.434831 | 0.168337 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844686 | CCATCCTGGCTAACA[C/G]GGCGAAACCCCGTCT | 115677 |
rs2461388 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841262 | ccaaaaaaaaaaaaa[A/G]aaaagaaaaagaaaG | 115677 |
rs2461389 | snp | C/G | 0.421694 | 0.181717 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818296 | AGCAGTGGCACACAC[C/G]TGCAGTCCTAGCTAC | 115677 |
rs2461390 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817379 | GGTAGCCCCTGCGGG[C/T]TCCCCACAAACCCCT | 115677 |
rs2555932 | snp | C/T | 0.450734 | 0.149016 | | | GRCh38.p7 | 2:168817469 | TAAATACCAGTCAAA[C/T]TGATCTGATTAAAAG | 115677 |
rs2632372 | snp | A/G | 0.444799 | 0.156695 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861031 | AAATTAATCGGTCCC[A/G]ATGGAAATATAAATT | 115677 |
rs2632380 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857840 | CAAAGAACTATTGAA[A/G]TTGCCAATCTGGGTA | 115677 |
rs2685798 | snp | A/G | 0.411074 | 0.191194 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843665 | GAAATCAAAATCATC[A/G]ATAAGCCTATGAAAC | 115677 |
rs2685799 | snp | C/T | 0.498525 | 0.0271165 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854794 | TGTCTGTAGCATTCG[C/T]GAATGCATGTGGTCT | 115677 |
rs2685800 | snp | C/T | 0.16846 | 0.236329 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861114 | GGTTGGGAAAGTATC[C/T]TATGAGAAGTTGCCT | 115677 |
rs2685801 | snp | G/T | 0.269538 | 0.249235 | intron-variant, missense, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863441 | CAGAATGATGCCAAA[G/T]AAAAAGTAGCTCTTG | 115677 |
rs2947934 | snp | A/G | 0.446902 | 0.154045 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839020 | GAACTCCTGACCACA[A/G]GTGATCTGCCCGACT | 115677 |
rs3216710 | in-del | -/A/AAA | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845807 | GACTTGGATTCTAAC[-/A/AAA]AAAAAAAAAAAAAAA | 115677 |
rs3732030 | snp | C/T | 0.237882 | 0.249706 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785119 | TGAAATGCTACAAAG[C/T]GAGTTTATTTTCTGT | 115677 |
rs3732031 | snp | C/T | 0.133947 | 0.221435 | synonymous-codon, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168824641 | TCTAACAGGGCAAAC[C/T]TGGAAATTAGCTATG | 115677 |
rs3821115 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803126 | GGATCACAAGTCCTG[A/C]AGGAGGAAGGATAGA | 115677 |
rs3843328 | snp | C/T | 0.424503 | 0.179021 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800485 | TGTCTGCCACTGGGC[C/T]GTTGTAAGGGCAGCA | 115677 |
rs3845725 | snp | C/G | 0.0505692 | 0.150756 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787307 | gagacagtgcccatg[C/G]ggagggatgaggatg | 115677 |
rs3845726 | snp | C/G | 0.285519 | 0.247464 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790112 | ACACGAGGCAAAGAG[C/G]GATGTCTTTGGAGAA | 115677 |
rs3845727 | snp | A/G | 0.350546 | 0.22889 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793861 | ATCAGCTGTGTTTAC[A/G]TAACAGAAACTATTC | 115677 |
rs3845728 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847823 | CTGTGCAAAGGAGAG[A/T]TCCATATCTAATGAT | 115677 |
rs3856426 | snp | C/T | 0.347914 | 0.230028 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789014 | aaccaagacctgggg[C/T]gctaggtgtgctcag | 115677 |
rs3914920 | snp | G/T | 0.342134 | 0.232404 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790196 | AAGTTGCCATAGCAT[G/T]TTATTATTGCTACAA | 115677 |
rs4000833 | in-del | -/ATCT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788893 | tctatctatctnnnn[-/ATCT]nnnttttatctGTGT | 115677 |
rs4109426 | snp | C/G | 0.489318 | 0.0722982 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794396 | CCACTGCACTCCAGC[C/G]TGGGCAACAGAGCGA | 115677 |
rs5836201 | in-del | -/A | 0.497933 | 0.032082 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788241 | GTAAGATCCTACCTC[-/A]AAAAAAAAAAAAAAA | 115677 |
rs5836204 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801471 | CAAGTGACCCTCTAG[-/G]CTCGGCCTCCCAAAG | 115677 |
rs5836205 | in-del | -/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818842 | TTAAAAAATTTTTTT[-/T]AATTTTTAATTTTTG | 115677 |
rs5836206 | in-del | -/A | 0.0607341 | 0.163335 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819046 | CAGTAGAATGGAAAG[-/A]AAAAAAATGCAAAAG | 115677 |
rs5836207 | in-del | -/A | 0.400682 | 0.199487 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822348 | CAGCTGTACTAAGAG[-/A]AAAAAAAAATGAATA | 115677 |
rs5836209 | in-del | -/TCTCTGGAAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850766 | GAAATTCTCTGGAAT[-/TCTCTGGAAT]CCATGATTGTGTCTC | 115677 |
rs6433093 | snp | A/C | 0.36955 | 0.219562 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802434 | TTCTCACTATCTCAC[A/C]CTGGCCGTCTTGACC | 115677 |
rs6715293 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806508 | GCTTACAAGTGCTGG[A/G]AAGAAACATTTTCCT | 115677 |
rs6716139 | snp | A/G | 0.351635 | 0.228408 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824267 | TGTGCATCTGTGTGT[A/G]TGTTTGGTTTGCTTG | 115677 |
rs6720808 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802741 | GATTTGTATATTAAT[G/T]GATTTTAACTTAAGA | 115677 |
rs6722317 | snp | A/G | 0.451359 | 0.148171 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790974 | GTATTTTTAATCAAT[A/G]TATTTGTTTTCTTTT | 115677 |
rs6722325 | snp | A/T | 0.45946 | 0.136478 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790993 | TTGTTTTCTTTTTTT[A/T]AAttttattattatt | 115677 |
rs6724279 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833407 | TTCCCAAGCTAAAAA[A/G]CCAAGGAAGAGAGAC | 115677 |
rs6724664 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833748 | ATGCCCAACTCTCAG[G/T]CTTGGCCATCAGGGA | 115677 |
rs6742716 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849059 | CATACTGAATCAGGC[C/T]AATGGGCTCCTGTAG | 115677 |
rs6746329 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849646 | taggcatgagccacc[A/G]cacctagccAGGCCT | 115677 |
rs6749871 | snp | C/T | 0.20111 | 0.245173 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796058 | AATCACTGCAATGAT[C/T]CCAGACTGAAAATAA | 115677 |
rs7562530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826637 | AGGCCACATGCTTGG[C/T]TCCTGTCCTGAGACC | 115677 |
rs7563765 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800601 | AGGAGTTTGGGGATA[A/G]GAGTGCCCTACCAAT | 115677 |
rs7566078 | snp | G/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827425 | AGCAGCAGCAGGACA[G/T]GAACAGGGCTCTCAA | 115677 |
rs7571674 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833131 | GTGACAGCGAAATTA[A/G]AGAACATAAAATTAT | 115677 |
rs7573108 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804922 | ataacattacagttg[C/T]tgcacatatctagaa | 115677 |
rs7583629 | snp | C/T | 0.280785 | 0.248097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816369 | ATTTTATAAAAGGGC[C/T]TTCGAGAGCTGAACT | 115677 |
rs7584086 | snp | C/T | 0.430583 | 0.172886 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786712 | gccagcttggccctc[C/T]tcgaagtgtacttta | 115677 |
rs7584277 | snp | A/G | 0.152334 | 0.230133 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786715 | agcttggccctcctc[A/G]aagtgtactttactt | 115677 |
rs7585565 | snp | C/T | 0.21875 | 0.248039 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833022 | ATAATGCTGAGAGGC[C/T]GCAATTGCTCCCAAG | 115677 |
rs7585708 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812010 | CTCTCCCCTCGAAGG[A/G]CAGAGGCAGTCTTAC | 115677 |
rs7588452 | snp | A/T | 0.424348 | 0.179172 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865434 | CAATTCCAAGAAGAG[A/T]GACAGGCAATCAAGA | 115677 |
rs7591036 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848395 | GGGCAGCTTCAGAGG[C/T]AACTAAGAAGATTGC | 115677 |
rs7591268 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818547 | TTAGTTTTACAAAAG[C/G]AGGATAGTCTAATAT | 115677 |
rs7595110 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849558 | acggggttttgccac[A/G]ttgggcaggctggcc | 115677 |
rs7595826 | snp | A/G | 0.209997 | 0.246779 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789986 | TGCCGCTGGTTTTTA[A/G]TCAGGCCACAGTGAG | 115677 |
rs7604904 | snp | G/T | 0.0131334 | 0.0799639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818206 | ctgctcaggctggag[G/T]gcagtggtgcaatta | 115677 |
rs9287902 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804260 | CCACTCCCTGGCATG[C/T]TGAATAGTTCCTTGT | 115677 |
rs9287903 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823612 | tatgggacacatcca[C/T]tatagggtttgggcc | 115677 |
rs9287904 | snp | A/G | 0.316243 | 0.241064 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832837 | ATGTTGCCCAGGCTG[A/G]TCCCGAACTCCTGGG | 115677 |
rs9789605 | snp | C/T | 0.226779 | 0.248919 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794454 | CCTCCCAGGTTCGCA[C/T]CATTCTCCTGCCTCA | 115677 |
rs10176220 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814651 | GAGGGTTATGACAGA[C/G]AATGATGAAGGCAAA | 115677 |
rs10182530 | snp | A/G | 0.125874 | 0.217008 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168857068 | GTGCACTTTAACCCA[A/G]TTAAGAAAAGCGACA | 115677 |
rs10182917 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824065 | gggcaacaagaggga[A/G]actccatctcaaaac | 115677 |
rs10198235 | snp | C/T | 0.252983 | 0.249982 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826200 | ATTACGTTTTTGATT[C/T]GAATTGCCTCCTAAG | 115677 |
rs10198395 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826223 | CTCCTAAGGAATGAG[A/G]GGTGTAGGGGTGTGT | 115677 |
rs10198693 | snp | A/G | 0.235854 | 0.249599 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826551 | TAAAAGATCAGTTAA[A/G]TGAGGGCCAGAGATT | 115677 |
rs10200152 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809171 | aaaagtagagagttg[A/G]gggctcgtgtggtgt | 115677 |
rs10203580 | snp | A/G | 0.0112044 | 0.0740043 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851067 | GCTGATCTTACCCCA[A/G]TTTTCATTCTTTTCA | 115677 |
rs10205264 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828556 | AGATTCCTGTGTTTA[A/G]CCCAGAAAAGGAAAA | 115677 |
rs10490707 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810235 | TGAAACTGCTTGGGA[C/T]ACAAGGAGAGTGGTG | 115677 |
rs10497348 | snp | A/G | 0.314301 | 0.241589 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861791 | GAAAGTGCATCATAA[A/G]TGGTTATTGAATCAA | 115677 |
rs10536098 | in-del | -/ATAT | 0.434743 | 0.168434 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841294 | TATTGAATGCTTTAA[-/ATAT]ATATATATAAAGTTG | 115677 |
rs10564930 | in-del | -/AG | 0.432944 | 0.170387 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787876 | ATAAACTGAAGCACA[-/AG]AGGGTAAAAACTTTG | 115677 |
rs10569466 | in-del | -/GACA | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863033 | TGTGAATAAAAGACA[-/GACA]TACTTCCCAGATGCC | 115677 |
rs10626753 | in-del | -/AGATAGAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798824 | GATCGATAGATAGAT[-/AGATAGAC]AGACAGACAGACAGA | 115677 |
rs10636938 | in-del | -/A/AA | 0.65169 | 0.0644319 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844393 | ACCTGTTTTAAGTTT[-/A/AA]AAAAAAAAAATGTTT | 115677 |
rs10650489 | in-del | -/AA/AAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849670 | AGGCCTTGTTTTTAC[-/AA/AAA]AAAAAAAAAAAAAAA | 115677 |
rs10661869 | in-del | -/A/AA/AAAA | 0.477175 | 0.104362 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855638 | AGAAAAAAGAAAGCC[-/A/AA/AAAA]AAAAAAAAAAAAAAA | 115677 |
rs10679511 | in-del | -/GAT | 0.424968 | 0.178567 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865777 | TCAGCAAAGTCTCAA[-/GAT]GATACAAAATCAATG | 115677 |
rs10679651 | in-del | -/A | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855654 | AAAAAAAAAAAAAAA[-/A]GGAAAATCACATTTT | 115677 |
rs10930337 | snp | C/T | 0.322007 | 0.239405 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838521 | ctgggattacaggcg[C/T]gagccaccgtgccca | 115677 |
rs11284678 | in-del | -/A | 0.433673 | 0.1696 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833817 | TCTTAAAACAATCTC[-/A]AATCGTGGCCTAGGT | 115677 |
rs11296225 | in-del | -/T | 0.183568 | 0.241012 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859358 | GAGTTTATTCCTCCA[-/T]TTTTTTTTCCTTCGG | 115677 |
rs11332007 | in-del | -/T | 0.34303 | 0.232046 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791749 | GATGGCCAGTGACGG[-/T]TTTTTTCATGTGTTT | 115677 |
rs11354593 | in-del | -/A | 0.475348 | 0.108251 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848561 | AAATGACTATATACC[-/A]AAAAACAAAATGTGG | 115677 |
rs11374385 | in-del | -/TTTGTTTGTTTGTTTG | 0.657954 | 0.0807721 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824768 | TTTTTTTATTTGTTT[-/TTTGTTTGTTTGTTTG]TTTGTTTGTTTGTTT | 115677 |
rs11385898 | in-del | -/A | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856575 | TCTTAAAAAAAAAAA[-/A]TCTCACTGGTATCAC | 115677 |
rs11408440 | in-del | -/A | 0.497613 | 0.0344622 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856574 | GCAAGACTCCGTCTT[-/A]AAAAAAAAAAATCTC | 115677 |
rs11424404 | in-del | -/A | 0.410399 | 0.191761 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845089 | AGGGGAACAAATGAG[-/A]AAAAAATTCCTTAAT | 115677 |
rs11424405 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844876 | AGAAAAAAAAAAAAA[-/A]GATTCAGCCTGGACC | 115677 |
rs11435789 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845090 | ACAAATGAGAAAAAA[-/A]TTCCTTAATTTACAC | 115677 |
rs11452657 | in-del | -/A/AA/AAA | 0.493837 | 0.055168 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820718 | GGAGAAAAGCTGGCC[-/A/AA/AAA]AAAAAAAAAAAAAAG | 115677 |
rs11676084 | snp | A/G | 0.163564 | 0.234582 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847464 | TCTAGATATTCTAAA[A/G]TTTGAGAGTCCCTGC | 115677 |
rs11678685 | snp | A/G | 0.352938 | 0.227824 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854097 | TGGTCTCGAACTCCT[A/G]ACCTCAAGTGATCCA | 115677 |
rs11893114 | snp | C/T | 0.196149 | 0.244131 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858017 | ATACCTGCAATGACC[C/T]GTGGCTACAGTTTTT | 115677 |
rs11896228 | snp | A/C | 0.029116 | 0.117091 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859906 | TACCTGAATTTCATC[A/C]TTTGGATGTGCTTTT | 115677 |
rs11898531 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843620 | TGATAATAATGGGCA[A/G]AATATGTCAGCAAGC | 115677 |
rs11898734 | snp | G/T | 0.127254 | 0.217792 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857730 | ATTTAAGGAGATAAA[G/T]TTTTTAGCAATGTTT | 115677 |
rs11899247 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812160 | TGTAAAGCTTTTCAC[C/T]GTGCTGAAATGAGCA | 115677 |
rs11899519 | snp | C/G | 0.187685 | 0.242109 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791792 | aatgtcttcttttga[C/G]aagtgtctgttcata | 115677 |
rs11899690 | snp | G/T | 0.377977 | 0.21476 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791980 | tgtgcagaagctctt[G/T]agtttaattagatcc | 115677 |
rs11900587 | snp | A/G | 0.115788 | 0.21092 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855603 | AACTTCAGTTGTGTG[A/G]ACAAAAAAAAAAAAA | 115677 |
rs12386224 | snp | C/G | 0.308414 | 0.24308 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837921 | ttagatttctttatg[C/G]gctcccttttttggc | 115677 |
rs12464371 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834519 | CGCGcacacacacac[A/G]cacacacacacacac | 115677 |
rs12464372 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834521 | CGcacacacacacac[A/G]cacacacacacacac | 115677 |
rs12469901 | snp | C/T | 0.00486615 | 0.0490856 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832455 | TGTTGAAATCCTTTT[C/T]CATCTCCAAAGCGTT | 115677 |
rs12471702 | snp | A/G | 0.00943375 | 0.0680285 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858658 | TTTAGTTTTGTCTTA[A/G]GTAAGCCTGCCCCAC | 115677 |
rs12612019 | snp | C/T | 0.491104 | 0.0660973 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797218 | CCTCAGCCTCCTGAA[C/T]AGCTGGGACTACAGG | 115677 |
rs12990061 | snp | A/C | 0.00477324 | 0.0486193 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788883 | tgcgtatacacacac[A/C]cagataaaaagatag | 115677 |
rs12993143 | snp | G/T | 0.414576 | 0.188188 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862990 | CATTTGCCAGTCATA[G/T]CTCTCCAGGCAATTA | 115677 |
rs13002530 | snp | C/T | 0.342582 | 0.232225 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820241 | CTTCCTTCCTATGTG[C/T]CCTCAGGCTAGTGAC | 115677 |
rs13016739 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862852 | AGAGTAACGTTATGG[A/G]AGAAAGAATATTATC | 115677 |
rs13017628 | snp | A/T | 0.333722 | 0.235565 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785365 | AGTTTTTAAGAGCAA[A/T]GAGTATTGTTTTTCT | 115677 |
rs13024314 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823584 | gtctgtttatgtcca[A/G]attttctctttatat | 115677 |
rs13025525 | snp | A/T | 0.146314 | 0.227484 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851798 | TGGCTTAAAACAAAC[A/T]TGTATTATCTCATAG | 115677 |
rs13028271 | snp | A/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839900 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 115677 |
rs13029623 | snp | A/T | 0.132066 | 0.220435 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848244 | TGATAGGCTATTCTG[A/T]GTCTTTAATCCTTTA | 115677 |
rs13032718 | snp | G/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836419 | CCATAACCTTGGCTG[G/T]TACTCTGTCATACAC | 115677 |
rs13034606 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840551 | aaaaaaaaaaaaaaa[A/C]caaaaaaaCAGATAT | 115677 |
rs13383073 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818170 | tattttatgtttttt[A/G]gagatggggttctca | 115677 |
rs13383882 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846270 | AATTTTATTATAAGT[A/G]TGAGAGATGGAAATG | 115677 |
rs13384117 | snp | A/C | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846589 | GTATTCTAGCCACAT[A/C]CCACCCTCCAAGAAG | 115677 |
rs13384876 | snp | A/G | 0.030053 | 0.118842 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834238 | CTAGGCCAAGAAGAA[A/G]TTAATGGTTAGTACC | 115677 |
rs13391714 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848867 | agatgaattatggtg[A/G]tgtttgcataataat | 115677 |
rs13396920 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797553 | GGCCAACATAAAGCT[A/G]TAAGGACTTCCCACT | 115677 |
rs13398166 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850176 | CCCTGGCCTCCCAAC[A/G]TGCTGGGATTATAGG | 115677 |
rs13402157 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844536 | TGTATTAATCATGAC[A/T]TTATGAGAACATTGA | 115677 |
rs13402190 | snp | C/T | 0.104149 | 0.203046 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851710 | AATCACTGTATATCA[C/T]GTGGTGCTTAAattg | 115677 |
rs13402324 | snp | C/T | 0.104149 | 0.203046 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851864 | aggtgtctctgaacc[C/T]ctcccaaggctgcaa | 115677 |
rs13405077 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848876 | atggtggtgtttgca[C/T]aataatgtgaatgca | 115677 |
rs13422562 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797471 | AGCAGTAGTACAAAG[A/G]CAAGAGTTCACTCTC | 115677 |
rs13431776 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845778 | TAAGACCTAGtttta[G/T]tttttttcttccttt | 115677 |
rs13431804 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805159 | AAAAAATTTAAAAAT[C/G]TCTTTTAGATCAAGC | 115677 |
rs16823013 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859100 | CAATTTCATTTGCGT[C/T]TATTGATGTTAATTC | 115677 |
rs16855872 | snp | A/G | 0.35207 | 0.228214 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786111 | GACATTGGTATCATC[A/G]TTATATCAAATATGT | 115677 |
rs16855876 | snp | A/C | 0.0248432 | 0.108648 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787712 | GTGAGAAGATGCCTC[A/C]GTTTTTGGAAAGGAA | 115677 |
rs16855886 | snp | G/T | 0.256061 | 0.249927 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790925 | AGGAAAAAAATCCTT[G/T]TAACGAACTTGCAAT | 115677 |
rs16855888 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793774 | TCTTCCAAGCCTCAT[G/T]AACTATAAGGTCCCA | 115677 |
rs16855893 | snp | C/T | 0.27008 | 0.249192 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796137 | GATTGGTGGAAGTGA[C/T]GTCATGTATGGTAAA | 115677 |
rs16855894 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796418 | CTTGGCTAAGTACTC[C/G]TGCTCACTTGGTCTT | 115677 |
rs16855906 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806183 | AGCACAGTGCCTGGC[A/G]TAGTAAAGGCAGTCA | 115677 |
rs16855919 | snp | A/C | 0.077417 | 0.180873 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808019 | GGCAATTGAGTTTTC[A/C]ATCACTGGCTTATAA | 115677 |
rs16855923 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808020 | GCAATTGAGTTTTCA[A/G]TCACTGGCTTATAAA | 115677 |
rs16855947 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815225 | CCTGGATATTCTGCA[A/G]TTCATGGTCATGCTT | 115677 |
rs16855994 | snp | C/G | 0.0252891 | 0.109567 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828240 | GTTCTCCCACCCTGG[C/G]CTTTCTCCAACTCCA | 115677 |
rs16856022 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834762 | GCCCACATTTTTTTA[A/G]AGGAAACTCTATTAA | 115677 |
rs16856027 | snp | A/G | 0.184838 | 0.241358 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846609 | CCTCCAAGAAGAAAC[A/G]CTTCAGATGATAGAA | 115677 |
rs16856030 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851503 | ATATCATGTTTTATC[A/C]ATGAAAATGATTTCT | 115677 |
rs16856039 | snp | A/G | 0.115788 | 0.21092 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856076 | ACCATAACGAGGAAG[A/G]AGCCAACGTTGGGTA | 115677 |
rs16856043 | snp | C/T | 0.117188 | 0.211804 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856841 | TATTTTTAGAATACT[C/T]GTTTCTGGTCCACTT | 115677 |
rs16856052 | snp | C/G | 0.125874 | 0.217008 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857975 | AAAATAGCCTGCATT[C/G]TGTGCACTGGGTAAC | 115677 |
rs16856059 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858072 | GACATTTTCTGTGAC[C/T]GCACAAGCTGTTTAG | 115677 |
rs16856061 | snp | C/T | 0.182933 | 0.240836 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859371 | CATTTTTTTTTCCTT[C/T]GGCATTTTCTGTGAA | 115677 |
rs16856065 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862819 | GCAGAGATCTGGAAA[C/T]GGAAGGGTTAGTGAG | 115677 |
rs16856067 | snp | A/G | 0.0345262 | 0.126772 | intron-variant, missense, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863432 | AAATCACCTCAGAAT[A/G]ATGCCAAATAAAAAG | 115677 |
rs17200181 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810944 | GGAAATTCTCGTGTC[C/T]GCAGGATAAATTCAA | 115677 |
rs17200279 | snp | A/G | 0.187685 | 0.242109 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813269 | AGCCAGGCATGTAAC[A/G]TGGGTTGTAGTCATC | 115677 |
rs17200300 | snp | C/T | 0.337614 | 0.234145 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813451 | TCACTGTTTTTCTTT[C/T]TTCTAGATCACTCCA | 115677 |
rs17265408 | snp | A/T | 0.128632 | 0.218563 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792854 | AAATGTTTATTAAAC[A/T]GTCGTTATGTATACT | 115677 |
rs17265731 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804475 | TCAAGTTGATTTCCT[A/G]GCACATTCTTAGCTT | 115677 |
rs17265836 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806787 | GATAGGGGGTTAGGA[C/T]ATTTAAAAGCTCAAT | 115677 |
rs17265885 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807613 | CAAGTATGAAGATCT[G/T]CTCAACTTGCATGTG | 115677 |
rs17265949 | snp | A/C | 0.102726 | 0.202016 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807948 | GTCCAGCAGCCCCTT[A/C]CTTTAAGAGGTTGAA | 115677 |
rs28576793 | snp | A/C | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798813 | GATCGATCGATCGAT[A/C]GATAGATAGATAGAC | 115677 |
rs28599777 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837164 | ACAAATAGTCTATTG[A/C]ATCTTCCTCCCATCT | 115677 |
rs28620900 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794038 | ATCTGTCTATCATAT[C/T]TATCATAATCTTCAT | 115677 |
rs28649748 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837973 | TTCTGAAGATTTCTC[A/T]TCTGGGCCTCACTCT | 115677 |
rs28652913 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833267 | TATTCATGCGTCACA[C/G]TCTCATTTCCCAGCA | 115677 |
rs28652992 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797084 | TTTCTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 115677 |
rs28675349 | snp | A/T | 0.308414 | 0.24308 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841452 | TCCAGAAGATTTAGT[A/T]ATCAGAATGACAAAT | 115677 |
rs28815499 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835299 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 115677 |
rs34056935 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861385 | ACACACCACACTGCT[C/T]TTCATCTTTCAGCAC | 115677 |
rs34073293 | snp | A/G | 0.0966768 | 0.197464 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168859604 | GATGGAATTACTACA[A/G]GGATGGCTGGGTTGA | 115677 |
rs34110248 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829260 | GGTTTTTCTTTCTTT[-/T]CCTTCCCTCCCTCCC | 115677 |
rs34186005 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796468 | GCCCCAAGCCCAGGG[-/G]CTGTCCCTTTACGGT | 115677 |
rs34211085 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811190 | TTATTTTGAAGTTTA[-/A]TATGTGCAGGAGGGG | 115677 |
rs34391896 | in-del | -/A/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820730 | GAGAAAAGCTGGCCA[-/A/AA]AAAAAAAAAAAAGCC | 115677 |
rs34494128 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832459 | AAATCCTTTTTCATC[-/C]TCCAAAGCGTTAGTG | 115677 |
rs34512271 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836492 | TGAAGCTGAACACCC[-/C]AAGCGGGGGGCATTC | 115677 |
rs34543087 | in-del | -/G | | | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856072 | AATACCATAACGAGG[-/G]AAGAAGCCAACGTTG | 115677 |
rs34573857 | in-del | -/A | 0.273049 | 0.248935 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864507 | GTCAGGCTGGTCTCG[-/A]AACTCCTGACCTTGT | 115677 |
rs34577612 | in-del | -/ATG/GAT | | | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865778 | CAGCAAAGTCTCAAG[-/ATG/GAT]ATACAAAATCAATGT | 115677 |
rs34604825 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851926 | AGGCTCTTCCTCCAG[-/T]AAGACTCACTTCCAA | 115677 |
rs34606910 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844394 | GTTTTAAGTTTAAAA[-/A]AAAAAATGTTTAAAG | 115677 |
rs34614546 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809647 | CCCTTAAACTTTCCC[-/C]AGTGTGCTGTAAGGG | 115677 |
rs34617989 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845462 | TGGGAGATAAATGGG[-/G]TCCTACCTGGTGTAG | 115677 |
rs34658144 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837858 | TTCTTTTCACTTTAG[-/G]TAACAACTAATGCTT | 115677 |
rs34821297 | in-del | -/C | 0.450734 | 0.149016 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817558 | TGCCTTTCTTGTCCA[-/C]TTTACCTGAATTCCC | 115677 |
rs34893393 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816479 | CCCATTTGCACCCCA[-/A]CTCACACTCCTGCAT | 115677 |
rs34898279 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838665 | GCTTTCAGTGTTGCC[-/C]TGTTCCTATCTATTC | 115677 |
rs34934545 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785698 | GCTGCATTGAAGGGG[-/G]TCTCAATACAGTTAG | 115677 |
rs34968373 | in-del | -/A | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787878 | AAACTGAAGCACAAG[-/A]GGTAAAAACTTTGTC | 115677 |
rs35066095 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795968 | TAAAAAATTTTTTTT[-/T]AAAATATGTGCATTA | 115677 |
rs35073023 | snp | A/C | 0.116488 | 0.211364 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859192 | CCTTCTACAATCAAC[A/C]CTTATCCCCTTTCTT | 115677 |
rs35140964 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834194 | ATCAGCCTCTGCTCC[-/C]TTTTTTTCTTGTTTG | 115677 |
rs35170382 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802918 | AAAAAGTTTTGAGAG[-/T]AGTAAAGCCTCATAT | 115677 |
rs35231741 | snp | G/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825806 | CTTTTGATGATGAAA[G/T]AGATAAGAAGGGGAA | 115677 |
rs35424978 | in-del | -/C | 0.333261 | 0.235728 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813015 | AGTCAAAAAGAGAAA[-/C]ATTTTAAATATGAAG | 115677 |
rs35448318 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787881 | ACTGAAGCACAAGGG[-/G]TAAAAACTTTGTCCT | 115677 |
rs35477906 | snp | A/G | 0.00446282 | 0.0470265 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851317 | GATATCTTTTTCAAT[A/G]TCAATCTTGCTGATG | 115677 |
rs35485658 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835701 | AAACACAGTGAGGGC[-/C]TAGGGCAGCTTTTCA | 115677 |
rs35561440 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803794 | AGTGAAACTTCCCCC[-/C]TTTAATTACTTCAAT | 115677 |
rs35577511 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795050 | CAATAAATAACCATT[-/C]TGGCATGCTTTTGTT | 115677 |
rs35584142 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828517 | TGAGTCCAAACCTTT[-/T]CTTTACTCTTCCTGT | 115677 |
rs35657408 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835714 | GCCTAGGGCAGCTTT[-/T]CAGGTTGCAGAATCC | 115677 |
rs35687851 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790730 | CCTGTTGCTATGGGG[-/G]AACTTAGGCAGGACA | 115677 |
rs35720867 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827738 | CACCTGGCTAATTTT[-/T]AAAAAGTTTTTCGTA | 115677 |
rs35742173 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828641 | ACTTTTATTTATTTT[-/T]AAAATAAATGAATAA | 115677 |
rs35762680 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846125 | TGTATACTCAGTCTA[C/T]ACCAGAAGGTCATTG | 115677 |
rs35785254 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809527 | TATAGAAGAAAACAA[-/C]AAGGCTTAGGGAGAA | 115677 |
rs35805236 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830539 | AGCATTCGCTAGATC[-/C]TCAGAGTGGTTGAAT | 115677 |
rs35809413 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806824 | AAAAGAACACCAAAA[-/A]TTGCCTTCCACCTGA | 115677 |
rs35922879 | in-del | -/TGAG | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863675 | GTGCAAAGCTGTGAG[-/TGAG]TTAAACTTTTGGCCT | 115677 |
rs35937085 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787857 | TTTTTTTAATTTTTT[-/T]CAGATAAACTGAAGC | 115677 |
rs35952103 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842081 | ATAATTTCTTTATGG[-/G]ACAGTTTTTACACAG | 115677 |
rs35981771 | in-del | -/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791090 | TGGTGTGCTGCACCC[-/C]ATTAACTCATCATTT | 115677 |
rs35998889 | in-del | -/T | 0.451234 | 0.14834 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785752 | TATTAGCTCTAAAGA[-/T]TTTTTTTTTTTTTTA | 115677 |
rs36018952 | in-del | -/T | 0.4444 | 0.15719 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797677 | AGTGTTAACCTTAAA[-/T]TTTTTTTTTTTTTAA | 115677 |
rs36083800 | snp | C/T | 0.431029 | 0.17242 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836904 | ACTCCCCCTGTCTTA[C/T]AGTCTGTTCAGGCTG | 115677 |
rs36086869 | in-del | -/A/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844403 | AGTTTAAAAAAAAAA[-/A/AA]TGTTTAAAGCAGATA | 115677 |
rs36117039 | in-del | -/A | | | intron-variant, frameshift-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850888 | AAGAGCCTGGGGAAA[-/A]GTGTGTGAGTGATTT | 115677 |
rs36186706 | in-del | -/C/CTTT/TTCT/TTCTT/TTT | 0.491368 | 0.0651254 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845790 | GTTTTTTTCTTCCTT[-/C/CTTT/TTCT/TTCTT/TTT]TTTTTTTTTTTTTTT | 115677 |
rs41268681 | snp | A/C/T | 9.7392e-05 | 0.0069777 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168802672 | CACTGACAGATTGTC[A/C/T]GGTGAGTAGCTCAGT | 115677 |
rs55687035 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800928 | AAAAAAACAAAAAAA[-/AA]GAGATGGGGTGTTGC | 115677 |
rs55786003 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839902 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 115677 |
rs55799749 | snp | A/G | 0.125874 | 0.217008 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794621 | CTCCCAAAGTGCTAG[A/G]CTTACAGGCGTGAGC | 115677 |
rs55824265 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834500 | TGGCGTGCGCGCGCG[C/T]GCGCGCGCACACACA | 115677 |
rs55875048 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817589 | TCACCACAATACTCC[C/T]TGTCCTCCCCTACCC | 115677 |
rs55910802 | snp | A/C | 0.348354 | 0.22984 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791213 | TGTTCTCATTGTTCA[A/C]TTCCCACCTGTGAGT | 115677 |
rs55980831 | snp | A/G | 0.38821 | 0.208322 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791357 | ATAGTATTCCATGGT[A/G]TATATGTGCCACATT | 115677 |
rs56022950 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796597 | TAACATTAGGGCACT[C/T]TTCGATTTTATTCTC | 115677 |
rs56323647 | in-del | -/GTTG/GTTT/GTTTC/GTTTTA/GTTTTT | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849922 | ACATTTTCTCATTTT[lengthTooLong]TTTTTTTTTTTTGAG | 115677 |
rs56326034 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839925 | TATATATATATATGT[A/G]TGTGTGTGTGTGTGT | 115677 |
rs56736605 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839923 | TATATATATATATAT[A/G]TGTGTGTGTGTGTGT | 115677 |
rs56960331 | snp | A/G | 0.310878 | 0.242475 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834503 | CGTGCGCGCGCGCGC[A/G]CGCGCACACACACAC | 115677 |
rs57302360 | in-del | -/GCGCGCACAC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834518 | CGCGCACACACACAC[-/GCGCGCACAC]ACACACACACACACA | 115677 |
rs57362666 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840540 | ATCTCAAAAAAAAAA[A/C]AAAAAAAAAAACAAA | 115677 |
rs57480764 | in-del | -/AAAAAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841253 | AAAAAAAAAAAAAAA[-/AAAAAAAAA]GAAAAGAAAAAGAAA | 115677 |
rs57492979 | snp | G/T | 0.231775 | 0.249335 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786836 | GTCAAATTCTTCCCT[G/T]CCTCCCCCCTCCTCC | 115677 |
rs57495214 | in-del | -/GGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814702 | AGATACAGTGAAGGA[-/GGA]CATGGGGTTTTGAAT | 115677 |
rs57620905 | in-del | -/CGATAGATAGAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798816 | GATCGATCGATCGAT[-/CGATAGATAGAT]AGATAGATAGACAGA | 115677 |
rs57650807 | in-del | -/TAGA/TAGACAGA | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798827 | CGATAGATAGATAGA[-/TAGA/TAGACAGA]CAGACAGACAGACAG | 115677 |
rs57797409 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841249 | CCAAAAAAAAAAAAA[-/AAAAAAAAAAAAA]GAAAAGAAAAAGAAA | 115677 |
rs57966954 | snp | G/T | 0.232651 | 0.249397 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791925 | AAATTTTCTCCCATT[G/T]TGTAGGTTGCCTGTT | 115677 |
rs58019132 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846562 | TTAGTCTTATTACTT[A/C]ACAATCATACTGTAT | 115677 |
rs58111829 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798593 | ATGCTGAGCAGAGAC[C/T]GAGAAAGAAAGCAGG | 115677 |
rs58191289 | snp | C/T | 0.157642 | 0.232314 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856086 | GGAAGAAGCCAACGT[C/T]GGGTAACTGTTAGCA | 115677 |
rs58305975 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786544 | TAAACACACTGCGCA[C/T]GCAGCCCTTCCCAAG | 115677 |
rs58341006 | in-del | -/AAAAAAAA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839895 | AAAAAAAAAAAAAAA[-/AAAAAAAA]TATATATATATATAT | 115677 |
rs58390009 | snp | C/T | 0.138546 | 0.223781 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841040 | GACAGATCGCTTGAG[C/T]CCAGGAGTTGGAGAC | 115677 |
rs58702721 | in-del | -/A/ACACACAA/ACACACACACAC/ACACACACACACACACACACCC/ACACACACCA/ACACACCC | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834542 | CACACACACACACAC[lengthTooLong]CACATACATTTTAAA | 115677 |
rs58854048 | snp | C/T | 0.255782 | 0.249933 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792069 | TGCCCATGCCTATGT[C/T]CTGAATGGTATTGCC | 115677 |
rs58865377 | snp | C/G | 0.422787 | 0.180679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840455 | GAATGGCGTGAACCC[C/G]GGAGGCGGAGCTTGC | 115677 |
rs58938408 | in-del | -/A | 0.430285 | 0.173197 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855605 | ACAAAAAAAAAAAAA[-/A]GTAGAAGAAAAAAGA | 115677 |
rs59115206 | snp | C/T | 0.125528 | 0.21681 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860222 | GTAAAAGTAATGCTA[C/T]GAATATTACTATTTG | 115677 |
rs59191977 | in-del | -/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841261 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAAAAGAAA | 115677 |
rs59235003 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840551 | AAAAAAAAAAAAAAA[-/A]CAAAAAAACAGATAT | 115677 |
rs59249410 | snp | A/G | 0.310878 | 0.242475 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834505 | TGCGCGCGCGCGCGC[A/G]CGCACACACACACAC | 115677 |
rs59344321 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805938 | CAGTGAGATGTGTAA[-/A]CATGCCATTCCACAT | 115677 |
rs59512579 | snp | A/G | 0.0644693 | 0.167566 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845129 | TGAACATAAGCTCCG[A/G]GTACTCTCTTGGTTT | 115677 |
rs59521327 | in-del | -/G/GTTTGTTC/GTTTGTTT/GTTTGTTTGCTA/GTTTGTTTGTTT | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824791 | TTTGTTTGTTTGTTT[lengthTooLong]TTTGAGACAGGGTCT | 115677 |
rs59686285 | snp | A/G | 0.158302 | 0.232576 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854025 | GGTGCACACCACCAC[A/G]CCCGGCTAATTTTTT | 115677 |
rs59995368 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834677 | TGGGACTACAGGAGC[A/G]TGCTACTTTGCCTGG | 115677 |
rs60011707 | in-del | -/GAGT | 0 | 0 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863676 | TGCAAAGCTGTGAGT[-/GAGT]TAAACTTTTGGCCTG | 115677 |
rs60068017 | in-del | -/T | 0.197082 | 0.244335 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864286 | CTGGCTGTGATCCTG[-/T]TTTTTTTTTTCTGAG | 115677 |
rs60232453 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840945 | GCATTTCAGGTCATT[G/T]CTAAATAGAGTAAAG | 115677 |
rs60303657 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819109 | CTTGTTTCTGACTAT[C/T]TTAATGAGGGAATGA | 115677 |
rs60336209 | in-del | -/A | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788936 | GATAGATAGATAGAT[-/A]GATAGATATTTCATA | 115677 |
rs60615208 | snp | A/G | 0.287085 | 0.247234 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856084 | GAGGAAGAAGCCAAC[A/G]TTGGGTAACTGTTAG | 115677 |
rs60668601 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849366 | TCTTTTCTTTTTTTT[-/T]GAGATGGAATCTCAC | 115677 |
rs60870015 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814801 | CTGGGTGCAGTGGCT[C/G]ATGCCTGTAATCCTA | 115677 |
rs60880453 | snp | A/G | 0.310878 | 0.242475 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834507 | CGCGCGCGCGCGCGC[A/G]CACACACACACACAC | 115677 |
rs61011647 | snp | C/T | 0.306927 | 0.243432 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841023 | TTTGGGAGGCTGAGG[C/T]AGACAGATCGCTTGA | 115677 |
rs61135592 | in-del | -/A/AAA | 0.375 | 0.216506 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849689 | AAAAAAAAAAAAAAA[-/A/AAA]GATGGGAAGAATTTT | 115677 |
rs61395235 | in-del | -/T/TT/TTT | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794369 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GAGATGGAGTCTCGC | 115677 |
rs61730433 | snp | C/T | 0.00578852 | 0.053486 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860907 | CAGGTTCTTCAACTC[C/T]AGGTAATCCCATGCC | 115677 |
rs62175689 | snp | A/G | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785906 | CAGGTGCATGCCACC[A/G]CACCCAGCTAATTTT | 115677 |
rs62175691 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794823 | AGGTCTCAAACTCCT[C/G]GGCTCAAGGGATCCT | 115677 |
rs62175692 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795409 | GTCCTTGTTCTCATG[C/G]TTTCCTTTGGAAGTT | 115677 |
rs62175693 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803110 | CATTTTTTGGAGTCA[A/C]GGATCACAAGTCCTG | 115677 |
rs62175720 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818354 | TAGAAATGGGATCTT[C/G]ATATGTTGCCTAGGC | 115677 |
rs62175721 | snp | A/C | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829600 | TGCTGGGATTACAGG[A/C]ATGAGCCACTGCCCT | 115677 |
rs62175722 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834509 | CGCGCGCGCGCGCGC[A/G]CACACACACACACAC | 115677 |
rs62175723 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837784 | CTTTCCAAGTCTTAC[C/T]TTAGTTAACTTCTCG | 115677 |
rs62175724 | snp | A/G | 0.067446 | 0.170804 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838606 | CTCTCTCAGGCCGCA[A/G]TCATCTTTTGCTTGG | 115677 |
rs62175726 | snp | C/T | 0.238749 | 0.249747 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848806 | GAAATGAGAAGTCGT[C/T]GTTTCATGGGTACGG | 115677 |
rs62175727 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854632 | TGCAACAGGTGTCTT[A/T]ATTGTTCCTGACACA | 115677 |
rs62175728 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854779 | TGCCTGCACTCGTGG[G/T]GTCTGTAGCATTCGT | 115677 |
rs62175729 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855348 | TCCTTCTTTTTTCCT[A/T]AAGGAAGAAGATCCT | 115677 |
rs62176769 | snp | G/T | 0.210909 | 0.246925 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864640 | TGTTCATTATCTTAC[G/T]CTTTTTAGTATCCTC | 115677 |
rs62176770 | snp | A/G | 0.158632 | 0.232706 | utr-variant-3-prime, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865130 | TGATTATTAGCTTGA[A/G]ACAGTCAGAAAAAAG | 115677 |
rs66678009 | in-del | -/GTGA | 0.162909 | 0.23434 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863670 | TTTCTGTGCAAAGCT[-/GTGA]GTGAGTTAAACTTTT | 115677 |
rs67119058 | in-del | -/AGAC | 0.163564 | 0.234582 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863028 | TCCTATGTGAATAAA[-/AGAC]AGACATACTTCCCAG | 115677 |
rs67216045 | in-del | -/GTAA | 0.414576 | 0.188188 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862544 | CTCTCTCAACTTAGT[-/GTAA]GTAAGTGCAAATTCT | 115677 |
rs67578978 | in-del | -/AAGT | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862550 | CAACTTAGTGTAAGT[-/AAGT]GCAAATTCTAGAACC | 115677 |
rs67661218 | in-del | -/TTT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794367 | GACAAAAGGGATGAT[-/TTT]TTTTTTTTTTTTTTT | 115677 |
rs71003057 | in-del | -/CTTTTC/CTTTTT/CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797083 | TTTCTTTTTTCTTTT[lengthTooLong]TTTTTTTTTTTTTTT | 115677 |
rs71003058 | in-del | -/AGGTATAG | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826222 | CTCCTAAGGAATGAG[-/AGGTATAG]GGGTGTAGGGGTGTG | 115677 |
rs71003059 | in-del | -/T/TT | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838804 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGGAGTTTTGC | 115677 |
rs71003060 | in-del | -/AA | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840550 | AAAAAAAAAAAAAAA[-/AA]CAAAAAAACAGATAT | 115677 |
rs71003061 | in-del | -/A | 0.499992 | 0.00199679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860676 | TCTAAAAAAAAAAAA[-/A]GAAAAAACAAACAGA | 115677 |
rs71297455 | multinucleotide-polymorphism | AGGTA/GGGTG | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826220 | CTCCTAAGGAATGAG[AGGTA/GGGTG]TAGGGGTGTAGGGGT | 115677 |
rs71297456 | in-del | -/GTTT/TT/TTTG/TTTGTA | 0.625 | 0.125 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849919 | CATTTTCTCATTTTG[-/GTTT/TT/TTTG/TTTGTA]TTTTTTTTTTTTTTT | 115677 |
rs71397665 | in-del | -/GATA | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788894 | ACACACAGATAAAAA[-/GATA]GATAGATAGATAGAT | 115677 |
rs71397666 | in-del | -/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832868 | ACAAGGGATCTGCCC[-/G]ACCTTGGCTTCCTAA | 115677 |
rs71405947 | multinucleotide-polymorphism | ACA/GCG | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834501 | CGTGCGCGCGCGCGC[ACA/GCG]CACACACACACACAC | 115677 |
rs71405948 | multinucleotide-polymorphism | ACA/GCG | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834509 | CACACACACACACAC[ACA/GCG]CACACACACACACAC | 115677 |
rs71430647 | snp | A/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797046 | AGACCATTGAACTCA[A/T]ACTTTTCTTTTCTTT | 115677 |
rs71430648 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830326 | TTCTGCATTGCCCCT[C/T]TCCACTGCACCCCAC | 115677 |
rs71430649 | snp | C/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844724 | AAATAGAAAAAATTA[C/G]CCGCGCGTGGTGGCG | 115677 |
rs71430650 | snp | G/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849331 | AATGCCCAGGCCTTG[G/T]ATTTTTTCTTTCTTT | 115677 |
rs71997437 | in-del | -/AAAA | | | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800911 | TCTAAATTTCTTTTA[-/AAAA]AAAAAAAAACAAAAA | 115677 |
rs72362785 | in-del | -/CA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834508 | GCGCGCGCGCGCGCG[-/CA]CACACACACACACAC | 115677 |
rs72532075 | in-del | -/A/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844402 | AAGTTWAAAAAAAAA[-/A/AA]ATGTTTAAAGCAGAT | 115677 |
rs72881759 | snp | A/C | 0.203882 | 0.245709 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786354 | CCGACAGACAGAAAA[A/C]ACCTGAAACTGGTTA | 115677 |
rs72881764 | snp | C/T | 0.125528 | 0.21681 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790044 | CAGATCGAGTTAGCT[C/T]ATTCTTGTTTTAGTC | 115677 |
rs72881773 | snp | G/T | 0.127944 | 0.218179 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793331 | CTAAATATTGGCCAG[G/T]CGCCATGGCTCACAC | 115677 |
rs72881776 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793651 | AATATCACAAATATG[C/T]GTAAGTTCCTATGTG | 115677 |
rs72881788 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798828 | CGATAGATAGATAGA[C/T]AGACAGACAGACAGA | 115677 |
rs72883256 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834690 | GCATGCTACTTTGCC[C/T]GGACCACATGTATTT | 115677 |
rs72883277 | snp | G/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845808 | TTTTTTTTTTTTTTT[G/T]TTAGAATCCAAGTCA | 115677 |
rs72883287 | snp | G/T | 0.489796 | 0.070696 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849923 | ACATTTTCTCATTTT[G/T]TTTTTTTTTTTGAGA | 115677 |
rs72883292 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853648 | CTTGCATTCCTTCAA[C/T]AGGGAAGGACTAATG | 115677 |
rs73030463 | snp | A/T | 0.030665 | 0.119967 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795881 | TGCCACAGTTTAAAG[A/T]ACTCATAAGTGCTTC | 115677 |
rs73032206 | snp | A/G | 0.203575 | 0.245652 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837027 | GGTTGCAGACCGGCT[A/G]CTTCTCATTGCATTC | 115677 |
rs73032218 | snp | A/G | 0.140581 | 0.224783 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843200 | GATTACAGTGACAAG[A/G]CCTGCCCTCTGTCTT | 115677 |
rs73032233 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852503 | ATTAATTACCAAAAC[C/T]TGCAGAAAGAATTCT | 115677 |
rs73969947 | snp | C/T | 0.0391387 | 0.134304 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785432 | CCCTGATGTACTACA[C/T]TTCTAGTGCTGCCAT | 115677 |
rs73969954 | snp | C/T | 0.0209421 | 0.100162 | utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168798184 | GATATGGAGAGCCAA[C/T]TGTATTTGTAAAACA | 115677 |
rs73969955 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800910 | TCTCTAAATTTCTTT[A/T]AAAAAAAAAACAAAA | 115677 |
rs73969958 | snp | A/C | 0.0260105 | 0.111035 | upstream-variant-2KB, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168802583 | CAGGACACACCCAAC[A/C]TTGATTACAGTGTCC | 115677 |
rs73969961 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810039 | GTGGGAGATCTGGCT[C/T]TCCTGGGCCACATTC | 115677 |
rs73969963 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815829 | GAACCACAAAGTCAA[C/T]ATGTCTAAAACAGGG | 115677 |
rs73969965 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822182 | GCGATGAGATATTTA[C/T]TGACTGGCTTCATTG | 115677 |
rs73969974 | snp | A/G | 0.0194373 | 0.0966481 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168834321 | CTGAGAAGGAGAAGC[A/G]GAAGGTAAGCTGTCA | 115677 |
rs73969978 | snp | A/T | 0.26326 | 0.249648 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836980 | TCTGGAAGTGTGGGA[A/T]CAGGTGCTATCTGGT | 115677 |
rs73969979 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840716 | GCCCTTAAATAGAGA[A/G]AGTCCATTTTAACAG | 115677 |
rs73969983 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847801 | ACAAGATAATAAAAA[G/T]CAAAAAATCATTAGA | 115677 |
rs73969985 | snp | A/T | 0.0664461 | 0.169729 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850597 | TGGAATTCTTCCCAA[A/T]TTTTTTTTTTTTTTT | 115677 |
rs73969989 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858817 | GGATAATGGTGAGGA[A/G]GGGGCTGGATAAGCA | 115677 |
rs73969992 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862569 | GCAAATTCTAGAACC[C/T]AGGTCAGCTGACTCC | 115677 |
rs74171274 | snp | A/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839914 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATG | 115677 |
rs74271846 | snp | G/T | 0.144632 | 0.226711 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840572 | AAACAGATATGTCCT[G/T]TGTAGGTCATGCATC | 115677 |
rs74271848 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844393 | CACCTGTTTTAAGTT[A/T]AAAAAAAAAATGTTT | 115677 |
rs74349012 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853172 | AACCATGAATCTGTT[A/G]TCTAAGAGAAAGGAC | 115677 |
rs74417284 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831645 | CTTCTAAGTGCTAAC[C/T]GAAGAGAAAAATGTT | 115677 |
rs74552507 | snp | A/C | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855605 | CTTCAGTTGTGTGAA[A/C]AAAAAAAAAAAAAGT | 115677 |
rs74607845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814022 | TTTTAGATCATGTAG[C/T]TAACCTGAAGGATGC | 115677 |
rs74665622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796159 | TATGGTAAACACTGC[C/T]ATGGCACTCATGTGC | 115677 |
rs74699922 | snp | G/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838804 | CTTTTTTTTTTTTTT[G/T]GAGACGGAGTTTTGC | 115677 |
rs74715539 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789392 | GGCATATCTTACGTG[A/G]CTGCAGGCAAGAGGG | 115677 |
rs74717607 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845601 | GTTAAGATCCTCTAC[A/G]TGTTTCCCCTACAAC | 115677 |
rs74728457 | snp | A/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855661 | AAAAAAAAAGGAAAA[A/T]CACATTTTGGTCTAT | 115677 |
rs74809037 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816115 | GTACAAAGGCACATG[A/G]CTGAGTGAGATGAAT | 115677 |
rs74831441 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797805 | CAACATGGTGAGACC[C/T]TGTCTCTACCTTGTG | 115677 |
rs74874485 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841297 | TGAATGCTTTAAATA[A/T]ATATATATAAAGTTG | 115677 |
rs74915043 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824316 | CAATTTTTTTTTTTT[G/T]GAGATGGAGTCTCGC | 115677 |
rs74945129 | snp | A/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837280 | ACATCTTTTTTTTTT[A/T]TAATACACTTTTTTA | 115677 |
rs75041997 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813725 | TCTCAAGAGTCTACT[C/G]GTTAGCAAAATTACA | 115677 |
rs75070331 | snp | G/T | 0.030665 | 0.119967 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827041 | AATCTGGCATCTTTT[G/T]GTCTAGTTCTCTTAT | 115677 |
rs75170284 | in-del | -/TTTAGTTGGCTAGAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832191 | TCAAGTAATTTAAAA[-/TTTAGTTGGCTAGAT]GACGTGTGCAGGAAA | 115677 |
rs75192387 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837673 | TCATCTTCTGTTCAC[G/T]CTTCAAATCACCCTA | 115677 |
rs75324682 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800882 | CATGTTATTAACCTC[A/T]GTCTATATCCTGTCT | 115677 |
rs75401852 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821688 | GAGGCAGTGATGTTC[A/G]AGCAGCTCCTGTTGG | 115677 |
rs75458689 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854608 | TTTCTTCCCCTATTT[G/T]TTTGCTCATGCAACA | 115677 |
rs75498213 | snp | A/C | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855606 | TTCAGTTGTGTGAAC[A/C]AAAAAAAAAAAAGTA | 115677 |
rs75627742 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801385 | ACCACCACATCCTAA[A/T]TAAAAAAAAAAAATT | 115677 |
rs75647545 | snp | G/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838805 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTTGCT | 115677 |
rs75691008 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815607 | ATGATTCATTGCGGA[C/T]ACTGTCAACAAAGCA | 115677 |
rs75738465 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861765 | TATAACATATGCAGT[C/G]CATACATATAGAAAG | 115677 |
rs75777276 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832370 | AGGAATTCATTTCAG[A/G]TAGAAAGGACTAGCA | 115677 |
rs75798003 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835460 | TCATGTGGGTAGTAA[A/C]AAACTCACAACCAGG | 115677 |
rs75920387 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830701 | GGAAAAAGTTAATTA[C/T]GATTAAGAGTTCAAT | 115677 |
rs75924697 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860159 | AATCTCAATCATTTA[C/T]AGGGTTGTGATCATT | 115677 |
rs75952027 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790160 | TGAGTATATTTCATG[A/G]AAAATATGATTGATT | 115677 |
rs75963289 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824317 | AATTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 115677 |
rs75965166 | snp | G/T | 0.0356815 | 0.128715 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785934 | TTTTTTGTATTTTTA[G/T]TAGAGATGGGGTTTC | 115677 |
rs75984170 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851537 | ACCCCATATAAATTT[A/T]AAAAACCCAGCATTC | 115677 |
rs76036428 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839184 | CGTCGTAAGCTGTGT[G/T]ATCCAACTTCACCAA | 115677 |
rs76099518 | snp | A/T | 0.030665 | 0.119967 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785334 | TCACCAAAGATGAGT[A/T]CAAAAGGGTCCCTAG | 115677 |
rs76216695 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812339 | GTTAAAACCATTTCA[A/G]ATTTAAAATAATGAA | 115677 |
rs76233100 | snp | A/C | 0.0441095 | 0.141807 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801474 | GTGACCCTCTAGGCT[A/C]GGCCTCCCAAAGTGC | 115677 |
rs76247276 | snp | A/C | 0.26818 | 0.249338 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794025 | TCATATCTTCATAAT[A/C]TGTCTATCATATCTA | 115677 |
rs76275826 | snp | C/T | 0.030665 | 0.119967 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785146 | CTGTAACTTGAGTTA[C/T]AGGAAATAAAAGAGC | 115677 |
rs76302666 | snp | A/C | 0.103794 | 0.20279 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861061 | TGTTAGACTCTGTAG[A/C]TTTATGTAAAAATGG | 115677 |
rs76397654 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841303 | CTTTAAATAWATATA[A/T]ATAAAGTTGGAGAAT | 115677 |
rs76408579 | snp | C/T | 0.465578 | 0.126594 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798824 | CGATCGATAGATAGA[C/T]AGACAGACAGACAGA | 115677 |
rs76492875 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820730 | GGCCAAAAAAAAAAA[A/G]AGCCCCAAATCACCT | 115677 |
rs76508936 | snp | A/C | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855637 | GAAGAAAAAAGAAAG[A/C]CAAAAAAAAAAAAAA | 115677 |
rs76522686 | snp | A/T | 0.00850636 | 0.0646593 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824760 | AATCAACCCTTTTTT[A/T]ATTTGTTTTTTGTTT | 115677 |
rs76604500 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861408 | TTCAGCACACACACA[C/T]GTGTCACTGTACCTG | 115677 |
rs76606586 | snp | G/T | 0.0196642 | 0.0971875 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818180 | TTTTTAGAGATGGGG[G/T]TCTCATTCTGCTGCT | 115677 |
rs76618709 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818757 | GACCAGCCTTGCATG[A/C]TGAGAGAAAATTAGA | 115677 |
rs76668933 | snp | A/G | 0.236144 | 0.249616 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787734 | GGAAAGGAAAAATGG[A/G]TTGATTTTTACATTT | 115677 |
rs76691844 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792658 | TTGTTTTTTGTATTT[C/T]TAGTAGAGACACAGT | 115677 |
rs76702193 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784929 | AAGGGCAAACATAAC[C/T]CAGAACACAGGTTCA | 115677 |
rs76713257 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824315 | TCAATTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 115677 |
rs76773141 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825166 | GTTCTTGGGCACTTA[C/T]TGTGTGCATGCACTG | 115677 |
rs76811860 | snp | C/T | 0.046775 | 0.145601 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826915 | GCAACCACTGACCTG[C/T]TTCCTGTCAATAGAG | 115677 |
rs76812170 | snp | C/T | 0.155656 | 0.231515 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841151 | AGCATTGCTTGAACC[C/T]GGGACAAGGAGGTTG | 115677 |
rs76853319 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853782 | TTGGGGTCAACTTGG[A/G/T]CCTTCTTTTATCTGT | 115677 |
rs76898086 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853504 | AATGTTAAGAGTTAA[A/G]TGATGGCAATATACC | 115677 |
rs76946655 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835030 | GGAGCAAGGTTCAGC[C/G]TTAACTATAGTAAAT | 115677 |
rs77035808 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791345 | TTTTATGGCTGCATA[A/G]TATTCCATGGTGTAT | 115677 |
rs77101923 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811284 | GTGACAGGAAACCAG[A/T]CTCCAAATGCACCCC | 115677 |
rs77113592 | snp | A/C | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798809 | CTTCGATCGATCGAT[A/C]GATCGATAGATAGAT | 115677 |
rs77213827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805789 | CCTGGATATCAGACA[A/G]TGACTGTCACTAACT | 115677 |
rs77259705 | snp | A/C | 0.224412 | 0.248687 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834541 | CACACACACACACAC[A/C]CCACATACATTTTAA | 115677 |
rs77414191 | snp | G/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852130 | AGAAGTGACATCTCA[G/T]CATATTCTATTTGCT | 115677 |
rs77432751 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843472 | ACTCATACAGTGATC[A/G]CTTATGGAGGTCAGG | 115677 |
rs77463321 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784664 | AAATTCTCCATTGGC[C/T]TTTTTTTTTAATCTA | 115677 |
rs77501730 | snp | A/T | 0.0376037 | 0.131863 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846188 | GTGTATGTTTATGGC[A/T]CTCAAGTGTCAAATG | 115677 |
rs77532742 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800411 | ATTCAAACATTCCTC[C/T]GAGAAGCTCAACAAA | 115677 |
rs77575079 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827598 | GGGGCTCAGGGGATA[C/T]GGTCTTGCTCTGTTG | 115677 |
rs77611988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828776 | AAATTCAAGCAATAG[A/G]ATAATTTGCAATGAT | 115677 |
rs77644297 | snp | A/G | | | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863818 | AAACCCTCAAAGTAC[A/G]GACACCAAGAAAGAG | 115677 |
rs77747836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832428 | CCCCTCTGAGAAGAC[C/T]TGTTCTCTAAGTGTT | 115677 |
rs77753714 | in-del | -/TTAGTTGGCTAGAT | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832192 | CAAGTAATTTAAAAT[-/TTAGTTGGCTAGAT]GACGTGTGCAGGAAA | 115677 |
rs77795351 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168802893 | GTCATCTTTCCTTCT[C/T]ATATTCTTGGAAAAA | 115677 |
rs77824647 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856901 | ATAGAACAATCTAGT[C/G]GGGGAGCTTATAGGG | 115677 |
rs77913489 | snp | A/C | 0.0659589 | 0.169201 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814051 | GCTTGTCCACACTAA[A/C]AGAGATGGCATTTGG | 115677 |
rs77917659 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834802 | AAAACCTCTCAGCTA[A/G]TACCCCAAATAAGTA | 115677 |
rs77969969 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168798219 | GAATGGTGCCTGACA[C/T]GTGGTATGTCCTTTA | 115677 |
rs78005721 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844059 | AACATGAATTAACCT[C/T]GAAAAACATGATGTT | 115677 |
rs78051255 | snp | C/T | 0.101301 | 0.200969 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842821 | CTTTAGGTTTGGCCA[C/T]GCCTTTTTTTCTTAT | 115677 |
rs78064561 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863033 | TGTGAATAAAAGACA[G/T]ACATACTTCCCAGAT | 115677 |
rs78107156 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804177 | CAAGTCTTCAGACGT[G/T]GAGAAATGTTTTCTT | 115677 |
rs78116661 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860008 | ATTAGTCTCATCTGT[G/T]TAAGATGGTGCCTAA | 115677 |
rs78150760 | snp | A/T | 0.030665 | 0.119967 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784571 | AACTTACACGTACTC[A/T]TTCTGGTTCATTACA | 115677 |
rs78154622 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833425 | AAGGAAGAGAGACCT[C/G]TCCTTTACTATCTGG | 115677 |
rs78156587 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848336 | GCCTCAGGGGACTGC[C/T]AGCGTAAACCAATCC | 115677 |
rs78223930 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842106 | ACACAGAAAGGCAGG[A/G]GAAAGTGAGACTAAT | 115677 |
rs78309881 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816413 | TACTTTCTCTCTTTC[C/T]GTCTCCCCATGATCC | 115677 |
rs78379101 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833396 | TTTGCCTTTGATTCC[C/G]AAGCTAAAAAGCCAA | 115677 |
rs78573157 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855185 | TTATTCATCAGGTCT[C/T]GAACAGGTAGAACAA | 115677 |
rs78579629 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853505 | ATGTTAAGAGTTAAA[G/T]GATGGCAATATACCC | 115677 |
rs78629098 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794122 | AAGGGATTGGCACTT[A/G]TTCCTCCTTGGATCT | 115677 |
rs78659627 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833705 | CCAACTCCAGCAAGT[A/G]CAGGGCATTTCACAA | 115677 |
rs78754217 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852391 | TGCCCCTTTGCTATA[C/T]TGGGGCAAATTATTT | 115677 |
rs78774207 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801271 | CTTTTTTTTTTTTTT[A/T]TTAGAAGTAGAGTCT | 115677 |
rs78828757 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789789 | CTTAAAGTAGCTGGT[A/G]CAAACTGAAAGTCAG | 115677 |
rs78862548 | snp | A/T | 0.0872718 | 0.189788 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795961 | GAAACCCTTAAAAAA[A/T]TTTTTTTAAAATATG | 115677 |
rs78941697 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826971 | CCTGTAATTGTAAGT[A/G]TATAGCAGGTATGCT | 115677 |
rs78951583 | snp | C/T | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846325 | ATTTTTTCTCCATTC[C/T]TTCACCATTCTTCTG | 115677 |
rs79003803 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820698 | CGGCAGAAACACTGG[A/G]GCACAGGAGAAAAGC | 115677 |
rs79074527 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844887 | AAAGAAAAAAAAAAA[-/AA]GATTCAGCCTGGACC | 115677 |
rs79078120 | snp | C/T | 0.0368353 | 0.130617 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845641 | CCCTTCTCAGCATTC[C/T]CAGTGTTTATGTTGA | 115677 |
rs79158722 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793146 | TCCAGTCCATCACCC[A/T]GTCTTGCTGGTTCCA | 115677 |
rs79210724 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821863 | AATCGGAGAGGCTGC[C/T]GGAGTCAGATCATGC | 115677 |
rs79257472 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793092 | AGAAACTTGGGCTTC[A/G]TTCTAGATTCCTCCC | 115677 |
rs79322152 | snp | C/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810374 | ATCCCCAAAGGTAGG[C/G]ACCTGGATTACCTCA | 115677 |
rs79364616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800281 | AGATTTGTGAACCAA[A/G]TAAAGTCTCTGTCAT | 115677 |
rs79373488 | in-del | -/AA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861497 | TTTAAAAAAAAAAAA[-/AA]GAACTTCAGTAAAAC | 115677 |
rs79471692 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840826 | CCATTTGCATCAGAA[C/T]GATCTGGGGAGCTAT | 115677 |
rs79487134 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861624 | ATGCCCCAAATATCC[C/T]GTATTTATACCTGAA | 115677 |
rs79589372 | snp | C/T | 0.0333695 | 0.124785 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168855995 | GTTTTATATGGACCA[C/T]GATAACTCATTGCAA | 115677 |
rs79632576 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801272 | TTTTTTTTTTTTTTT[G/T]TAGAAGTAGAGTCTC | 115677 |
rs79698442 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801387 | CACCACATCCTAATT[A/T]AAAAAAAAAAATTAT | 115677 |
rs79836445 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787743 | AAATGGGTTGATTTT[C/T]ACATTTTGAATTTAA | 115677 |
rs79864086 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809620 | GCAGGTCTTCTCACA[A/C]TTTGAAAATACTCCC | 115677 |
rs79894654 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836599 | TTCCTGCTCAGCAGT[C/G]TTGATTCCCACCAGA | 115677 |
rs79905909 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839141 | TTGAACCTTGCCAAT[C/G]TCTTCAACATCACCT | 115677 |
rs79926792 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814862 | CTTGAGGCCAGGAGT[C/T]TGAGACCAGCCTGTT | 115677 |
rs80075099 | snp | A/G | 0.000792676 | 0.0198925 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811612 | TTTTCTCAAAATGGA[A/G]AGAATTTCTGCAAAC | 115677 |
rs80252114 | snp | C/T | 0.0554779 | 0.157039 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785811 | TGGAGTGCAGTGGCA[C/T]GGGATCTCAGCTCAC | 115677 |
rs80302539 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822348 | CAGCTGTACTAAGAG[A/G]AAAAAAAAATGAATA | 115677 |
rs80310369 | snp | A/G | 0.0263992 | 0.111815 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786619 | GAATCAGGAGAAAAG[A/G]GATGCAAGATCCCAG | 115677 |
rs80322747 | snp | A/G | 0.039522 | 0.134904 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833220 | AAGTAGTCTATTTGG[A/G]AGACTCTAATGAAAA | 115677 |
rs80351979 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804750 | AACTCAGTGGGTTGC[A/G]TGAACTTCAGTGAAA | 115677 |
rs111292306 | in-del | -/TATG | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168846156 | ACTCACATATTACTC[-/TATG]TATGCCATATTTTGT | 115677 |
rs111296427 | in-del | -/A | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817154 | CAGATGGGGATATGG[-/A]AAAGATGATACATTT | 115677 |
rs111352163 | snp | A/C | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840544 | CAAAAAAAAAAAAAA[A/C]AAAAAAACAAAAAAA | 115677 |
rs111445963 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843457 | TAGGCATGAGTGATG[A/G]CTCATACAGTGATCG | 115677 |
rs111460032 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793422 | AAACCAGCCTGGGCA[A/G]TATGGTGAAACCTCA | 115677 |
rs111460265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808650 | CTAAATAAATCAAAT[A/G]AGAAAGCCACAGGAC | 115677 |
rs111591478 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812365 | ATGAATGTGTGCCAT[A/G]AGACCAAAGATGCCA | 115677 |
rs111596685 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854390 | TTGAGTCATTAGTTT[C/T]CCGTCTTTCTCCATG | 115677 |
rs111599029 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857454 | CTTTAAGGGTGGGAA[C/T]TGGGGTGGGGAGATG | 115677 |
rs111680696 | snp | C/G | 0.039522 | 0.134904 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807283 | ATACACACACACACA[C/G]AGAGAGAGAGAACTA | 115677 |
rs111698524 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827160 | CCTCTTCATCAAAAT[C/G]TACACAGGCCTCTGT | 115677 |
rs111709283 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824303 | AGCCAGCATAATCAA[-/T]TTTTTTTTTTTTTGA | 115677 |
rs111791987 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863255 | TCTTGTTAATAGATT[A/G]TGTCAATTTACTGAC | 115677 |
rs111832413 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827767 | TAGAGAAAAGGTCTC[A/G]CTGTGTGTGTTGCAC | 115677 |
rs111845579 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787251 | CCCCACTTCCTACCA[C/G]CTGTTCTCCCCCTTA | 115677 |
rs111856325 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851095 | TCAGAGCATTCTGGA[A/G]CTGGAGAAGGAAAGA | 115677 |
rs111883175 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799129 | AACTCAGGAGCTTCC[A/T]CTTCCTCTTCTTTTC | 115677 |
rs111886175 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862381 | ATGTCACAGGCTGTG[A/G]CAACACAAGATTTGA | 115677 |
rs111901561 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796481 | GGGCTGTCCCTTTAC[A/G]GTCATCTTGCTGTGA | 115677 |
rs111906637 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791455 | CCACAATAAACATAC[A/C/G]TGTGCTTTGTGTTTA | 115677 |
rs111906828 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859150 | AGCACTGATGGCTCA[C/T]CTTCTTCGCAGACCA | 115677 |
rs111935346 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789461 | CTCATGAGACTTATT[C/T]ACTGTCATGAGAACA | 115677 |
rs111941046 | in-del | -/C | 0.0448719 | 0.142907 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841404 | TTTCAGCTACCCTGG[-/C]CCAGGGAGTTTTATA | 115677 |
rs111954799 | in-del | -/A | 0.125874 | 0.217008 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806573 | AGTTGTCTATTTGAG[-/A]AGGGGTTATTATTTT | 115677 |
rs112080349 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805815 | TAACTCAGATGGTGC[C/T]GGTGCCATGGTCCGT | 115677 |
rs112149171 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816414 | ACTTTCTCTCTTTCC[A/G]TCTCCCCATGATCCC | 115677 |
rs112164878 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796191 | TGCAGTGACAACAGG[A/G]AACGCTGCTGCTCCT | 115677 |
rs112273399 | snp | C/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818744 | ATGAAAATATATTGA[C/G]CAGCCTTGCATGCTG | 115677 |
rs112325660 | snp | G/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824964 | GGGTCTTACTATGTT[G/T]CCCAGGCTGGTCTTG | 115677 |
rs112359045 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851980 | GGCCTCCAGTCCTCG[C/T]TGCTGTTGGTTGGAG | 115677 |
rs112410588 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787848 | GATTTTCATTTTTTT[A/T]AATTTTTTTCAGATA | 115677 |
rs112438419 | snp | C/T | 0.0105982 | 0.0720194 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850996 | TGAGACTTTGTTCAG[C/T]CTGTCTTCAGGTGTG | 115677 |
rs112465105 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823263 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 115677 |
rs112472394 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789316 | TATAAAGGAAAGAGG[C/T]TTAATAGGCTCACAG | 115677 |
rs112477530 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853943 | CACAATGTCAGCTCA[A/C]TGCAACCTCTGCCTC | 115677 |
rs112576886 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835060 | TTTAAATGCATATTT[C/T]GAATAGTCTTCTTGA | 115677 |
rs112581213 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787633 | ATCAGCCACAGTGTC[C/T]ACTACACAGCAGGTG | 115677 |
rs112602633 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801398 | ATTAAAAAAAAAAAA[-/A]TTATAGAGATAGGAA | 115677 |
rs112608747 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855558 | TTTGCTATTTGGCAG[A/G]GGTCTTCTCATTTAA | 115677 |
rs112687215 | in-del | -/GT | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839939 | TGTGTGTGTGTGTGT[-/GT]ATGAGTATACATTCT | 115677 |
rs112752019 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836631 | GCTGATCTAAACCTC[C/G]GTTCTCCTCACACCT | 115677 |
rs112760430 | snp | A/C | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840378 | TACTAAAAATACAAA[A/C]AATTAGCCGGGCGTG | 115677 |
rs112764677 | snp | G/T | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799363 | TACAAGATTCTTTGC[G/T]CCTCTTACTCACATG | 115677 |
rs112824275 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816846 | AATAGATGCTCACTG[A/G]GTAAATGAAGGCACT | 115677 |
rs112874255 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811220 | GCATAAAATAGTTAC[A/G]TGGTGTCCTTCAGAA | 115677 |
rs112930632 | snp | C/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841044 | GATCGCTTGAGCCCA[C/G]GAGTTGGAGACCAGA | 115677 |
rs112975750 | snp | C/T | 0.000182278 | 0.00954492 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851198 | GTGAGTAGAGATGAT[C/T]TCTCCATTTCTGGTA | 115677 |
rs113027495 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834502 | GCGTGCGCGCGCGCG[C/T]GCGCGCACACACACA | 115677 |
rs113089158 | in-del | -/AGGGGTGT | 0.476635 | 0.25462 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826220 | GGGGTGTAGGGGTGT[-/AGGGGTGT]GTGTATTGTGTTACA | 115677 |
rs113111021 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845756 | CAACTTCAGCTCTAA[A/G]AATATTTAAGACCTA | 115677 |
rs113137969 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827471 | ACTTTTCTGAGTCTC[A/G]GTTTTTTCATATCTA | 115677 |
rs113177097 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831869 | TTCAGTAATTTTCCC[A/G]AGGATACAGAGCTGG | 115677 |
rs113210755 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796268 | CCGGGAGTTGGCCTT[A/C/T]GGAAGACATGTTAAG | 115677 |
rs113221727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854022 | ACAGGTGCACACCAC[C/T]ACGCCCGGCTAATTT | 115677 |
rs113232568 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822935 | GCCAACGATTATAAT[A/C]TAGAGCTAATCTGAT | 115677 |
rs113235305 | snp | A/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789389 | AAAGGCATATCTTAC[A/G]TGGCTGCAGGCAAGA | 115677 |
rs113268968 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843471 | GACTCATACAGTGAT[C/T]GCTTATGGAGGTCAG | 115677 |
rs113367076 | snp | C/T | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812699 | GTGGGAAGGTAAATA[C/T]ACGGGAAGAGTAAAG | 115677 |
rs113440271 | in-del | -/AAG | 0.125182 | 0.216612 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168859763 | TTCATGCAGTTAGTT[-/AAG]AAGATAAATGTTTTT | 115677 |
rs113458955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851478 | CTTACATTGAAAAAA[C/T]TGAAAGCAAATATCA | 115677 |
rs113579432 | snp | C/G | 0.5 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168809402 | GGTTATAGATCAAAG[C/G]GGGAGGGAGGCTGAG | 115677 |
rs113590063 | snp | A/G | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835394 | AGCCTTCTCGATAAT[A/G]TAATTTGTTCATCAA | 115677 |
rs113703870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819324 | AGGAATCCTGAAAGG[A/T]TACATATACTGCCTC | 115677 |
rs113729443 | snp | A/C | 0 | 0 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863031 | TATGTGAATAAAAGA[A/C]AGACATACTTCCCAG | 115677 |
rs113749088 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839170 | CTCTCCCCATTCTCC[A/G]TCGTAAGCTGTGTGA | 115677 |
rs113749579 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789595 | AGATCCAAACCGTAT[C/T]AGCTGGAGTGTGCCT | 115677 |
rs113757953 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838486 | ATCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 115677 |
rs113796303 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852954 | CTGAGATGGAAAAAT[A/G]TACAATAAAATAAAT | 115677 |
rs113925452 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833787 | GTGACCCTTGCTGCA[C/T]GTTTTAAGAGAACAT | 115677 |
rs114071543 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831845 | TTGGGCAATGGAGAC[A/G]CAGAGAGTTTCAGTA | 115677 |
rs114139854 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844961 | GGCTATATGGCAGGC[A/G]GAAACCCAACGGCTG | 115677 |
rs114197404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856170 | CAATCAAGATGCTTT[A/C]AGCACCAGCACTTCT | 115677 |
rs114207286 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792682 | ACACAGTTTTCGCCA[C/T]GTTGCTCAGGCTAGT | 115677 |
rs114259122 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825397 | TATTTAACTTGGGAA[A/G]TGGTGTTGTTAAAGT | 115677 |
rs114267915 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845503 | GCTTGCCTTCTTCAA[C/T]ATATGTTAGGGAAGG | 115677 |
rs114374633 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795378 | TGTAATTTGAACAAA[C/T]CTGCATTTGTAAAAT | 115677 |
rs114375128 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864229 | TAATCTGCCCATCGC[A/G]GCCTCCCAACGTGCT | 115677 |
rs114376065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847067 | CAACATTAAAGGGAT[A/G]ACTAAGTGAATAAAC | 115677 |
rs114390268 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788284 | TGATGACTTTTTCTT[C/G]TTCCTTTTTCTTTTT | 115677 |
rs114431721 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789201 | TATGAGGACATAGAA[C/T]CAACTAAAATCTAGG | 115677 |
rs114444109 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820948 | GAGGCTGTGACTGAC[A/T]GTGTTACCTTTCCTG | 115677 |
rs114448341 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841573 | ACTTGCAGTGAACAT[G/T]GGGCATGTATCTCAG | 115677 |
rs114473412 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814950 | ATAGTTAAGGGTTTT[A/T]AAAAATTATTATATC | 115677 |
rs114537885 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790643 | GGAAAGCCAAGGAGG[A/G]GCTAAGAACTGTTCC | 115677 |
rs114600953 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836538 | ATAGAAGCGCTCATG[A/T]TCACCTGAGCTGATG | 115677 |
rs114646233 | snp | A/C/G | 0.0123036 | 0.0774623 | utr-variant-5-prime, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788010 | TTTGGGGGATGAGAA[A/C/G]AAGAAGATAAATCAG | 115677 |
rs114655261 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824833 | CTGGGTTAGAGTGCA[G/T]TGGCACAATCACAGC | 115677 |
rs114709581 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862127 | ACCCTGTCTTAGTGT[A/G]GCAGCCTTAAGAGTT | 115677 |
rs114717993 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788526 | GGGAGTGAGGAGTTG[G/T]AGGAGGAAGCATGAA | 115677 |
rs114723444 | snp | A/G | 0.081446 | 0.184634 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849905 | GCATGGGTCCAATAA[A/G]TAACATTTTCTCATT | 115677 |
rs114749463 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834001 | AAAAAGTATGCAGGA[A/G]TTCTCCGGACAAAGT | 115677 |
rs114787764 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825867 | TTTCCACTCTTCTTT[A/G]GGCATCAGCCATAAT | 115677 |
rs114824750 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820069 | AGGTGAAGTGAGAGG[C/T]GGTATCAATTTTTGA | 115677 |
rs114915383 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861186 | GTTATTTGCCATAAA[C/T]ATAATCACACCTAAA | 115677 |
rs114928708 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800464 | CTGGATTCAGCTGGG[A/G]TGCCCTGCTGCCCTT | 115677 |
rs114930332 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821010 | ACGGACAAGAAAACG[G/T]GATTCTTCCTCCCAC | 115677 |
rs115074387 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835927 | ACCCCTCTTGTGGTA[C/T]GTGTCCCAGATTGAA | 115677 |
rs115205482 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788225 | CAGCCAGAGTGACAG[A/G]GTAAGATCCTACCTC | 115677 |
rs115228466 | snp | C/T | 0.084364 | 0.187256 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864226 | GCCTAATCTGCCCAT[C/T]GCGGCCTCCCAACGT | 115677 |
rs115244107 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837867 | ACTTTAGTAACAACT[A/G]ATGCTTTTATTTTCC | 115677 |
rs115310536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816729 | TACACCCTGCACTGT[A/C]ATTCTCTGTTCACTT | 115677 |
rs115323374 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788968 | CTGTCCACCTCAGAG[C/T]CTAGAGTCAATGCCT | 115677 |
rs115406628 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834118 | AGGATTCTAGGATAC[A/G]TAATTGTTAAAGCTA | 115677 |
rs115450265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820175 | GTGTGGTTAAGCAGG[C/T]AGTTCCCCAGCCAGA | 115677 |
rs115478693 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845320 | TCCTTGGATGGCCCT[C/G]TTAGGAGATGGGAGA | 115677 |
rs115625712 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827241 | AGACTACATGGGGCC[A/G]CTGTGGAAGAAAAAT | 115677 |
rs115635726 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812057 | ACCTCTTAGAGCCTG[A/G]CCTTTTGATTTCCTT | 115677 |
rs115660930 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831834 | CATTTTACAGATTGG[A/G]CAATGGAGACACAGA | 115677 |
rs115661673 | snp | C/T | | | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864297 | CCTGTTTTTTTTTTT[C/T]TGAGACAGAGTCTTG | 115677 |
rs115740077 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803739 | TTTGTGCTTAATGTA[A/G]AAACAAATTCCAATG | 115677 |
rs115753610 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168812532 | TTAATACATGCTATA[C/T]CCATCACATGGGAGA | 115677 |
rs115842552 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788728 | GGAAAAGGGAGGTGT[A/C]AATATGGAGGAAGAG | 115677 |
rs115843980 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818598 | CTTACATTTTAATTA[A/G]CGCTTTATCTAAAAT | 115677 |
rs115845969 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794136 | TGTTCCTCCTTGGAT[C/G]TCTCGTTAATGCCTG | 115677 |
rs115851015 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827606 | GGGGATACGGTCTTG[C/T]TCTGTTGCCCAGGCT | 115677 |
rs115927756 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823869 | GTCACCTGAGGTCAG[A/G]CGTTTGAGACCAGCT | 115677 |
rs115990336 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816291 | TTTCACTCTGTAGCC[A/G]TGACCCTGTTTAAGA | 115677 |
rs116059642 | snp | C/T | 0.00375395 | 0.0431611 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860868 | ATATTGTGAGCAAGG[C/T]ATCTTCTGGTGGGCA | 115677 |
rs116090559 | snp | C/G | 0.0126979 | 0.078662 | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786486 | TAGGAACGTTAGATT[C/G]GTAATAGAAGAACGT | 115677 |
rs116121062 | snp | C/G | 0.0103295 | 0.0711199 | downstream-variant-500B, missense | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865390 | CTATGAGGGGGTCAA[C/G]CAGAGCCTGGGAGAT | 115677 |
rs116248616 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788836 | TGAACACAGATGTTA[A/G]GTGTGTATATGCATT | 115677 |
rs116304183 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800974 | GGTCTCGAACTCCTG[A/G]CCTCAAGCAGTCTTC | 115677 |
rs116331304 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797909 | AATAAGTTAATAAGT[C/T]ATCCCGCAGTATCCA | 115677 |
rs116347880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848613 | TATTCAGCCAAAAAG[A/G]AAGGGAATTCTGGCA | 115677 |
rs116370961 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852504 | TTAATTACCAAAACC[C/T]GCAGAAAGAATTCTG | 115677 |
rs116388859 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803191 | ACTGGTTTAGCAGCA[C/T]GTTTGTTCCATGTTT | 115677 |
rs116469775 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847084 | CTAAGTGAATAAACA[C/T]GCCTGCACCATGGAT | 115677 |
rs116523616 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796332 | GTCCTAGGAAGAAAG[C/T]GCTCTTGAAGATGTG | 115677 |
rs116527261 | snp | A/C/T | 0.0558253 | 0.159067 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838529 | ACAGGCGCGAGCCAC[A/C/T]GTGCCCAGCCCCAAA | 115677 |
rs116541559 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789946 | GGGGCACCCACAGGC[C/T]GTGGGAAATATGATG | 115677 |
rs116543162 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829789 | TGACCAGGTGCAGGT[A/G]AGATGTTTGTAAGCT | 115677 |
rs116576282 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852432 | GTCAAGCCTCAAAGA[C/T]TTTGGCCTCTGCTCC | 115677 |
rs116577451 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820983 | AAACCATTCAGGATT[A/G]TTCTGGAGCCAACGG | 115677 |
rs116609322 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844116 | AATCTGTGTAAATCA[A/G]CATTCTTTTAAACTC | 115677 |
rs116649685 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798683 | CCAGAGTATGAGTGC[A/G]GGTCAGAAATGTAGG | 115677 |
rs116650257 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832760 | TGCCATGGATTTTAT[G/T]AGTTTTCTTTAAAAG | 115677 |
rs116734316 | snp | A/T | 0.0391387 | 0.134304 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863569 | ATTTGAATCATTGCT[A/T]TAAAAAATATTGTCT | 115677 |
rs116802367 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843280 | TCATTGTTTCAGTTT[C/T]TCCATGGATACAATT | 115677 |
rs116821929 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829619 | AGCCACTGCCCTCGG[C/T]CTAGAACAGTTTCAT | 115677 |
rs116841798 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860182 | TGATCATTTCACTTG[C/T]ATTAAGCCAACTAAA | 115677 |
rs116849393 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797037 | GTGGGAGGCAGACCA[C/T]TGAACTCATACTTTT | 115677 |
rs117103019 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168843491 | ATGGAGGTCAGGCAT[C/T]GTGTTAGGCACTGGA | 115677 |
rs117151377 | snp | A/G | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844875 | ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAAAAGA | 115677 |
rs117192494 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838573 | TCTTTGCTTTTGTCT[A/G]TCTCCACTGCTGACA | 115677 |
rs117384552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816206 | CCTTTAGAAGACCCC[A/G]TTTCCAATCCAAGCA | 115677 |
rs117394461 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865054 | AAGTGCTCTTACCTT[C/T]ACATGTTTTTCTTTT | 115677 |
rs117408911 | snp | A/T | 0.0368353 | 0.130617 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844940 | ATTGAAAACTGGGAG[A/T]GCAAAGGCTATATGG | 115677 |
rs117439705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798439 | ATACTTCATAAATGC[A/G]TACTCATGTTGTTAA | 115677 |
rs117507175 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806226 | GTGTTAAATTTAAGG[A/G]GAATATCATGGTTTC | 115677 |
rs117561412 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794077 | ATAGAGTAATATAAC[C/T]TTCCTTCATCAAACT | 115677 |
rs117564856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858522 | ATTGTTGAGAAAACT[G/T]GAGGCACTTAGATTA | 115677 |
rs117624361 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823307 | AGGCGTGAGCCACCG[C/T]GCCCGGCCAGTTGCA | 115677 |
rs117667685 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819347 | ACTGCCTCATTAGAC[C/T]GGAAGCATGGAAGAG | 115677 |
rs117678579 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168813552 | TGAAGTCTCTTCCTA[A/G]GGCTGCCATCTGCCC | 115677 |
rs117802235 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168856420 | TCTCTACTAAAAATA[C/T]GAAAATTAGCCGGAC | 115677 |
rs117906058 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844235 | ATGGTGGGAATACAA[C/T]AGAACTGCCAGAAAC | 115677 |
rs117945234 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839065 | GCTGGGATTACGGGC[A/G]TGAACCACCACACCC | 115677 |
rs118103537 | snp | A/C/T | 0.0226779 | 0.104054 | intron-variant, missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850945 | GAAATCTCCCTCCAC[A/C/T]ATGGTTTGGATATGA | 115677 |
rs137877657 | snp | A/G | 4.97657e-05 | 0.00498802 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851227 | TATGCCTGGTAAGAA[A/G]GGGCAGAAACCTTTC | 115677 |
rs137917467 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845969 | CAGCTTCTCCTACCC[C/T]ACCTTCCTCTGAGTT | 115677 |
rs137969911 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816917 | AATGAAGATCAAGTT[A/G]GGCTATTTTTGAGGA | 115677 |
rs137990311 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844902 | AAGATTCAGCCTGGA[C/T]CTCTGCATTATGCTC | 115677 |
rs137992015 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799784 | TATACCAGCCACCTG[C/T]TCCTTGTCCTTGCTG | 115677 |
rs138073658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840192 | GTTAATGTTCACAAG[C/G]TTGAGTTTCTACAGA | 115677 |
rs138079462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810590 | AATATGGTGCCCAAC[G/T]GAATGCTGGCGATAT | 115677 |
rs138175032 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836050 | AAAATTGTCATCACC[A/C]GTAGCTCTTTCATCT | 115677 |
rs138245800 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790807 | TTCCTGCTTTTGATG[G/T]TTGTATTTTGGTTTT | 115677 |
rs138247824 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795020 | GCCTCTCAGTTGCTG[C/T]CACAGGAAAAAATCA | 115677 |
rs138293199 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831602 | TTTTGCTTTCATACA[A/C]ATGCGATGACATGTT | 115677 |
rs138295865 | snp | C/G | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865561 | CTTTGAAAACTGGCA[C/G]AAGACAGGAATGTCC | 115677 |
rs138298295 | in-del | -/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857700 | ATGAGTGGACTGGGG[-/G]TTAATCTGAGAATCA | 115677 |
rs138388408 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168864426 | GAGTAGCTGGTATTA[C/T]AGGCGTGCGCCACCA | 115677 |
rs138391616 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820734 | AAAAAAAAAAAAAGC[C/T]CCAAATCACCTCAAA | 115677 |
rs138417157 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860613 | GAGGTGGAGGTTGTA[A/G]TGGGCCAAGATCATG | 115677 |
rs138432429 | snp | A/G | 0.00013301 | 0.00815396 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168851318 | ATCAGCAAGATTGAC[A/G]TTGAAAAAGATATCC | 115677 |
rs138498345 | in-del | -/TG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825541 | TAATATGTGCTCTAT[-/TG]TGTGTGTGTGGGCAT | 115677 |
rs138576559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823872 | ACCTGAGGTCAGGCG[C/T]TTGAGACCAGCTGAA | 115677 |
rs138607448 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816515 | CCACCACCACCACAC[A/G]TGGGTCCCTGCATTT | 115677 |
rs138612061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805657 | AGCAAGTCTTCTGGG[C/T]GCCACACAGTCAGCC | 115677 |
rs138631446 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845440 | CCCTTCTACCTACAT[C/T]GCAGCAATGGGAGAT | 115677 |
rs138649571 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836535 | CACATAGAAGCGCTC[A/C]TGATCACCTGAGCTG | 115677 |
rs138754477 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799704 | TATTTCTCTTCCTAA[C/T]GCCAGTCTGCTGAGG | 115677 |
rs138802742 | in-del | -/GA | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845999 | TCTCTCCTGCCTCCT[-/GA]GAGCCATCTCAAGCC | 115677 |
rs138859026 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839695 | GAGGTGGGCAGATTA[C/T]CTGAGGTCAGGAGTT | 115677 |
rs138862361 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826698 | TCTACCCAGAAATGT[A/G]CCTGACTTCATTTTT | 115677 |
rs138895291 | in-del | -/AGG | 0.0360663 | 0.129354 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814698 | TTCAAGATACAGTGA[-/AGG]AGGACATGGGGTTTT | 115677 |
rs138919942 | snp | G/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785392 | TTCTCTCAGCTGAGG[G/T]TACTAGATGGTACAT | 115677 |
rs138947288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819509 | GGGGAAGAATTTAAC[C/T]GTTAACATCTGTTGA | 115677 |
rs138985035 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824456 | GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTG | 115677 |
rs139128272 | snp | A/G | 8.28384e-05 | 0.00643524 | missense, utr-variant-5-prime, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168828168 | TTTAGTTGTGTTAGC[A/G]GTGCCTGGGCCTGGG | 115677 |
rs139239630 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168824971 | ACTATGTTGCCCAGG[C/T]TGGTCTTGAACTCCT | 115677 |
rs139331194 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835472 | TAACAAACTCACAAC[C/T]AGGAGAGGTGGCAGC | 115677 |
rs139350147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168796310 | CGTGTCACCCATGTC[A/G]TAGCTAGTCCTAGGA | 115677 |
rs139390221 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792467 | TTTTATTTTATTTTT[C/T]GAGATGGAGTCCCGC | 115677 |
rs139463032 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837414 | TTCTGGGTTCATGAC[A/G]TTCTCCTGCCTCAGC | 115677 |
rs139522169 | snp | G/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826238 | GGGTGTAGGGGTGTG[G/T]GTATTGTGTTACAGC | 115677 |
rs139555229 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842446 | AGCTAGGACCAGGAC[C/T]CTTATCCTGGAAGTT | 115677 |
rs139593927 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838321 | CTCAGCTCACTGCAA[C/G]CTCTGCCTTCCAGTT | 115677 |
rs139630098 | in-del | -/T/TT/TTT | 0.431621 | 0.171796 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794353 | AGACAAAAGGGATGA[-/T/TT/TTT]ATTTTTTTTTTTTTT | 115677 |
rs139676324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789483 | ATGAGAACAGCACAA[A/G]AAGCACCTGCCCCAA | 115677 |
rs139677426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861703 | TTATACAATGATGTT[C/T]TTCTCTAGACTTGCT | 115677 |
rs139704477 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817521 | ATAAAATTTTGTTTC[C/T]CTGCTGAAAAGCTTG | 115677 |
rs139707092 | in-del | -/AATTCTCTGG | 0.363359 | 0.222822 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850753 | CCCCATCTCTACTGA[-/AATTCTCTGG]AATTCTCTGGAATCC | 115677 |
rs139754316 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856068 | ATGTGAATACCATAA[C/T]GAGGAAGAAGCCAAC | 115677 |
rs139765492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853891 | TTATTTATTTGAGAC[A/G]GAGTCTCGCTCTGTG | 115677 |
rs139776859 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168852448 | TTTGGCCTCTGCTCC[C/T]CTCTTGATATTCTTA | 115677 |
rs139893948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807844 | GGACAAAAGTTAGAA[A/C]GTACTGGTCTATGAA | 115677 |
rs139967057 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862118 | ATGAATAAAACCCTG[G/T]CTTAGTGTGGCAGCC | 115677 |
rs139986455 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168849064 | TGAATCAGGCCAATG[C/G]GCTCCTGTAGGAATT | 115677 |
rs140006175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817848 | AGCAAGTGAGCCAGC[A/C]ACTCCAATGACAGAG | 115677 |
rs140008410 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857299 | TTATTAAGGTGGTAT[C/T]TTCCATTCATCCCTC | 115677 |
rs140050796 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802168 | GGCCAGTTGTTTGCT[C/G]TCTCTAGGAATTAGC | 115677 |
rs140087198 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844098 | GAAATATACCACTTA[C/T]ACAATCTGTGTAAAT | 115677 |
rs140170212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821632 | AATAAAACTGTAAGG[G/T]GAGAGTGGCGAGGAT | 115677 |
rs140216390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790028 | CTAACAGGCCCCCAG[A/C]CAGATCGAGTTAGCT | 115677 |
rs140228595 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794052 | TCTATCATAATCTTC[A/C]TAATCTGTCATAGAG | 115677 |
rs140236634 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830148 | ACTAGTCTATATTTC[A/G]TTGATTACAAAATAT | 115677 |
rs140236658 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787771 | TAAGCTGATGAGAGT[A/C]CTTTCATGTGGACAT | 115677 |
rs140283947 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826479 | TGCTTCCTTCGTTCC[C/T]TCTCTTTCCATTTTT | 115677 |
rs140340863 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810945 | GAAATTCTCGTGTCC[A/G]CAGGATAAATTCAAA | 115677 |
rs140360007 | snp | C/T | 0.000116489 | 0.00763092 | intron-variant, synonymous-codon, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168850844 | AACTTAGGTAACCCA[C/T]AGCATCTGCCTATAT | 115677 |
rs140387300 | snp | G/T | 0.0711525 | 0.174681 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823085 | GCAGTGGCGCAATCT[G/T]GGCTCACTGCAACCT | 115677 |
rs140412762 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | NOSTRIN | GRCh38.p7 | 2:168863579 | TTGCTTTAAAAAATA[C/T]TGTCTCCAAATTGAT | 115677 |
rs140448868 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803847 | ATTGTGAATAATTTT[C/T]AAGAAGTCTTTTATC | 115677 |
rs140472033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822284 | CTAGGCCTTAGCATA[C/T]ATCCTGCAATGACTT | 115677 |
rs140513240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863138 | CTGTTGGTTGCAAAG[C/T]CTACTTATACTTTAT | 115677 |
rs140740513 | in-del | -/ACAAG | 0.089084 | 0.191327 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862385 | ACAGGCTGTGGCAAC[-/ACAAG]ACAAGATTTGAACTT | 115677 |
rs140796206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830688 | GTTTAAAAGCAAGGG[A/G]AAAAGTTAATTATGA | 115677 |
rs140802500 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793080 | GAGGAAGATACCAGA[A/G]ACTTGGGCTTCGTTC | 115677 |
rs140809953 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825144 | ATAACATCAAGCATG[A/G]CTTCCAGTTCTTGGG | 115677 |
rs140837241 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844936 | CCCCATTGAAAACTG[A/G]GAGAGCAAAGGCTAT | 115677 |
rs140856417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864167 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 115677 |
rs140881096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787221 | GCATAGCGTGAAGCA[C/G]TGAGGCAGCCTCCAC | 115677 |
rs140901400 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826019 | TAAATTCTAACTCTA[A/C]CACTTAACAGGTGAG | 115677 |
rs140902897 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790582 | TCCAAATTGAAGGAC[A/G]TTACATAAAATAATT | 115677 |
rs140979969 | in-del | -/C | 0.0341408 | 0.126114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854468 | CTCTACCATCCTATT[-/C]TTTTTTATTCAATCC | 115677 |
rs141116392 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799510 | ATGCCTCACCTACCT[A/G]AGCCTCAGTGGCTGA | 115677 |
rs141141494 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168841918 | AGGGGTGTAATCTAA[A/T]GCTAATAGACTGTGT | 115677 |
rs141177220 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854751 | GTCTTCTTGCCTCCT[C/T]GAAGCTGTCAGCTGC | 115677 |
rs141199959 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785042 | TTTAGGGATCTGGGT[C/T]TTAAGAATGGGCTGA | 115677 |
rs141220802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814552 | GAAACTATCTTGTTA[C/T]TTAAGGTTACAGACA | 115677 |
rs141293121 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808842 | GATTTAAAAAGAAAT[A/G]TAATTAGACAAATGT | 115677 |
rs141295538 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786515 | GTCTCAAGTGAGCAT[A/G]CGTATAACTCCCGTA | 115677 |
rs141466190 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819843 | CAGCCCAGAGGGCTA[A/G/T]CTCGGTGACATTTGC | 115677 |
rs141484544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795827 | CAAATTAGGCTGGCT[A/G]TTAACAATAACAGCA | 115677 |
rs141554484 | snp | A/G | 0.000732308 | 0.0191211 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824610 | AGCCCAGTACATCCT[A/G]TTTAACTAGTCCTTT | 115677 |
rs141597163 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864663 | GTATCCTCTGGATTA[G/T]GCCTGCTTTATACAC | 115677 |
rs141659981 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168820071 | GTGAAGTGAGAGGCG[G/T]TATCAATTTTTGAAA | 115677 |
rs141667979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824089 | TCAAAACAAAAAACA[A/G]AAAAACAAAAACAGA | 115677 |
rs141765347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837185 | CCTCCCATCTTGCAA[A/G]AGTAAAGAAAGTTAC | 115677 |
rs141887892 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835537 | GTTAAATTGTTGGTA[G/T]TAACATCAATCCACA | 115677 |
rs141976509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789342 | CACAGTTCCACATGG[A/G]TGGGGAGACCTCATA | 115677 |
rs142024594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826994 | GGTATGCTCTTGTGC[C/T]TAAGCTTGTATCTGG | 115677 |
rs142071030 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839840 | GTAGTGAGCTGAGAT[C/T]GCACCACTGTACTCC | 115677 |
rs142098215 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168793186 | TCTACCACTGCCACC[G/T]GGGTTAGTTAAGGCC | 115677 |
rs142117431 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835265 | TGCATTTTTAGTAGA[C/G]GCGAGGTGTCACCAT | 115677 |
rs142123955 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168855566 | TTGGCAGGGGTCTTC[C/T]CATTTAAAGAACCAT | 115677 |
rs142166791 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785412 | AGATGGTACATAGAA[C/G]TGAGCCCTGATGTAC | 115677 |
rs142173926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818976 | GCATCACCAATTTCA[C/T]ACAGGCCAAGACAAT | 115677 |
rs142195031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789861 | CTGCCAGCTCTGAGC[A/G]TATTTTCTGAACCAG | 115677 |
rs142199375 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863142 | TGGTTGCAAAGCCTA[A/C]TTATACTTTATATTC | 115677 |
rs142244931 | snp | C/T | 0.0425829 | 0.139564 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800952 | GTGTTGCTATGTTGA[C/T]CAGGCTGGTCTCGAA | 115677 |
rs142262592 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844726 | ATAGAAAAAATTAGC[C/T]GCGCGTGGTGGCGGG | 115677 |
rs142264804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817894 | GTCTTTCAAGTTGCC[A/G]GTAATGAACTTTAAA | 115677 |
rs142265183 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816307 | TGACCCTGTTTAAGA[C/T]GCTTCAAAGACTCCT | 115677 |
rs142269151 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858167 | ATTGTCATTACCAGC[A/G]TACATGTATTAGGAT | 115677 |
rs142308715 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168856938 | TCATAAGTCATTTGA[A/G/T]GGATCTGGAAAAATA | 115677 |
rs142394448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168811953 | CTGATGCATAGTCTC[A/G]TTATTGTACTTTTCA | 115677 |
rs142495856 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788143 | ACATTGGGAGGCCAA[A/G]GCAGGAGAAATGCTT | 115677 |
rs142499836 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860488 | GCAGCCTGGCTGACA[C/T]GGTGAAACCCCGTCT | 115677 |
rs142557808 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168835448 | GTGTTTGCCCTTTCA[C/T]GTGGGTAGTAACAAA | 115677 |
rs142576252 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800125 | CAGCTGATGAAATAC[A/G]GCCTCAGCCAACAGC | 115677 |
rs142594302 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168831708 | CACCAAACCAATGGA[A/G]GTGCATGGCTCTAAC | 115677 |
rs142660804 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825600 | CTTAGCACATTAGGT[A/T]CTGAAAGGTATTGGT | 115677 |
rs142708032 | in-del | -/GATA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168798813 | ATCGATCGATCGATC[-/GATA]GATAGATAGATAGAC | 115677 |
rs142711497 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816563 | TGCCTGGTAGATGTT[G/T]CATCACCTTCATTGC | 115677 |
rs142713206 | snp | A/C | 0.021333 | 0.101051 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837372 | TGGAGTGCAGTGGCG[A/C]GATCTCGGCTTACTG | 115677 |
rs142731354 | snp | A/G | 2.24323e-05 | 0.00334898 | missense, intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168811583 | ATAATAAAGTATACA[A/G]GAACCTAAAGGAGTT | 115677 |
rs142847684 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822051 | CCTGGGGTTCCAGAG[C/T]ATCTGAGTTCATCAA | 115677 |
rs142878982 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804707 | CTACTGTTCTTAACC[G/T]GGCCCACACCAATGT | 115677 |
rs142915800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847862 | ATTTCCTCCTCTTCT[A/T]ATGAGCAAACATAGA | 115677 |
rs143014547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789730 | GAAAATCAAATATAT[G/T]AGGAAAAGTAGAAGT | 115677 |
rs143016667 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832822 | AGACAGGGTCTTGCT[A/G]TGTTGCCCAGGCTGA | 115677 |
rs143019304 | snp | C/T | 0.00172234 | 0.0292951 | missense, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168860825 | TATGTGAAAATATCT[C/T]GGCCTTTTTTAATGA | 115677 |
rs143057404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168827632 | AGGCTGGAGTACAGT[A/G]GCATGATCATAGCTC | 115677 |
rs143060882 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823577 | TGTACATGTCTGTTT[A/G]TGTCCAAATTTTCTC | 115677 |
rs143129299 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850557 | TTCCAAGACATGGAT[A/G]TGGGCTTTCCTGGGC | 115677 |
rs143166986 | in-del | -/TTCTTTAT | 0.470618 | 0.117591 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862756 | CTCAACCTTCTTTAT[-/TTCTTTAT]GTGTCCAGTTAGAAA | 115677 |
rs143291825 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168836381 | AAGATCCACAGTGCT[C/G]TCTCCTCTCCTCCAG | 115677 |
rs143311726 | in-del | -/TA | | | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786456 | GGGGAGTTTAACTGG[-/TA]TATGACCTTCCTCTA | 115677 |
rs143344450 | snp | C/T | 0.124144 | 0.21601 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791341 | CCCTTTTTATGGCTG[C/T]ATAGTATTCCATGGT | 115677 |
rs143356535 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864564 | TGCTGGGATTACAGG[C/T]GTCACCCACCACGCC | 115677 |
rs143374973 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168791140 | AATGCTATCCCTCCC[C/T]GCTTTCCCCACCCCA | 115677 |
rs143436068 | snp | C/T | 0.00189105 | 0.0306912 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851267 | CTTATTCTGTTCCCC[C/T]TGGCATTGCAGTGCC | 115677 |
rs143436147 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168806682 | TTTTTTTCCCCAATA[A/G]TTAATGGTCCCCAGG | 115677 |
rs143442163 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819885 | CCATCCTTCCCACTT[A/T]GCCAGACCCTCAACA | 115677 |
rs143474960 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, missense | NOSTRIN | GRCh38.p7 | 2:168846920 | CTCAGGACAGTAGGG[C/G]TTCATTCTTTCCTAG | 115677 |
rs143526517 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829748 | TGGCTCTGATAGGGG[C/T]GGGGTTATGGTCACT | 115677 |
rs143540215 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815641 | AAAAATTGAAATTAA[A/G]TATTTGAAAAATAAT | 115677 |
rs143665176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814991 | GAAGAAGGCCTTTAT[C/T]GTCCTTGGAGGTATG | 115677 |
rs143761074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810697 | TCTTATGTAAAATCT[C/T]ATTTTGAAAAATGCA | 115677 |
rs143800735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826774 | ACCCATTTTAAGCAT[A/G]TGATTTGATCAGTTT | 115677 |
rs143823706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838723 | TTAAACTCGAATCTG[A/G]GCATATCATTCCTTT | 115677 |
rs143869345 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168851812 | CATGTATTATCTCAT[A/G]GTTTATGTGGGTCAG | 115677 |
rs143890740 | snp | C/G | 0.00874735 | 0.0655527 | downstream-variant-500B, intron-variant | NOSTRIN, SPC25 | GRCh38.p7 | 2:168865587 | TGTCCTCTCACCACT[C/G]CTATTCAACATAGTG | 115677 |
rs144028436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168830521 | TGGAAAAAAATGAAA[C/G]TGTAGCATTCGCTAG | 115677 |
rs144066967 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829477 | AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 115677 |
rs144162662 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840800 | ATGTTTTTTAAAGAA[C/T]GGTTTGAAGACCATT | 115677 |
rs144175522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792645 | TGTTTGTTTTGTTTT[C/G]TTTTTTGTATTTTTA | 115677 |
rs144190001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168853484 | ATCTTTAGAAGAGAA[A/G]GACAAATGTTAAGAG | 115677 |
rs144199968 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | NOSTRIN | GRCh38.p7 | 2:168856611 | ATCACTTCTAGGCTC[A/C]CTTTGAGAGCGACCG | 115677 |
rs144268624 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795297 | ATTTGTAAGACTGAT[C/T]GCAGATGAGCTTAAT | 115677 |
rs144356484 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807517 | GGGGGAATTTTTGGC[A/G]TATAGTATATAGGAT | 115677 |
rs144384301 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168822540 | AAATAATTCTAAAAT[A/G]TAATAAAAATGGATT | 115677 |
rs144456591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817604 | CTGTCCTCCCCTACC[C/T]CACACACAAATGCAC | 115677 |
rs144549135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814209 | GGATCATTTCTCTCC[C/T]ACACAGTGACGTGAT | 115677 |
rs144591271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826122 | TGTGAGAATTAAATA[C/T]GGTAATATAAGACGT | 115677 |
rs144610736 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805826 | GTGCCGGTGCCATGG[C/T]CCGTAGCTCCTAGGA | 115677 |
rs144670744 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786374 | GAAACTGGTTATCAG[C/T]AGCGTCCCAATAAGA | 115677 |
rs144674740 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168821851 | GGCAGGAAGGGAAAT[C/T]GGAGAGGCTGCCGGA | 115677 |
rs144684462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168864228 | CTAATCTGCCCATCG[C/T]GGCCTCCCAACGTGC | 115677 |
rs144696455 | snp | C/G | 1.65875e-05 | 0.00287984 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861922 | ATATTCATTTGCCTG[C/G]TAACACAGCATACTA | 115677 |
rs144760290 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825172 | GGGCACTTACTGTGT[A/G]CATGCACTGTGTTAA | 115677 |
rs144766770 | in-del | -/TCTT | | | intron-variant, downstream-variant-500B | NOSTRIN, SPC25 | GRCh38.p7 | 2:168864591 | GCCCAGCCAATCCTG[-/TCTT]TCTTTAAGCAATTAT | 115677 |
rs144771541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168805613 | TGCTTTTTACACACT[C/T]ATACAGTATCCAGGA | 115677 |
rs144780182 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817400 | AGGGGCTACCTCAGG[A/G]GGTGAGGAGGAGGTT | 115677 |
rs144801146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168838389 | GGAGTACAGGCGTGC[A/G]CCATCACATCTGGCT | 115677 |
rs144801768 | in-del | -/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832796 | GTTTTGTATTTTTTT[-/T]AAAGAAATAGAGACA | 115677 |
rs144834041 | in-del | -/TAGA | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788900 | GATAAAAAGATAGAT[-/TAGA]AGATAGATAGATAGA | 115677 |
rs144868009 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168823238 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 115677 |
rs144909214 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834773 | TTTAAAGGAAACTCT[A/C]TTAATATCTTAAAAA | 115677 |
rs144968440 | in-del | -/AT | 0.0379877 | 0.132479 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818953 | GGGTTGCCTATCAAA[-/AT]ATATATGCATCACCA | 115677 |
rs144995206 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789808 | ACTGAAAGTCAGACC[A/G]AGAAACAAAGGGCCT | 115677 |
rs145059658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810121 | CGGTCCTCACCCTCC[C/T]CCTCACTCATTCAGG | 115677 |
rs145086610 | snp | A/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797674 | ATAAGTGTTAACCTT[A/T]AATTTTTTTTTTTTT | 115677 |
rs145107636 | snp | C/T | | | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168824297 | GATTTCCAGCCAGCA[C/T]AATCAATTTTTTTTT | 115677 |
rs145171469 | in-del | -/TATAA | 0.00517822 | 0.0506191 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168861730 | TGCTATTTCATGTAT[-/TATAA]TATAGTTTTTGGTTA | 115677 |
rs145174576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842512 | AAAGTAAAATAATAT[C/T]GCTAGATAGGACAGT | 115677 |
rs145219055 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168857881 | ACAGATGCAGTGAGG[C/T]ATCGCTGACCTAGTT | 115677 |
rs145219326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786844 | CTTCCCTGCCTCCCC[C/T]CTCCTCCAGAGTAGC | 115677 |
rs145224351 | in-del | -/GCGC | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834491 | AATCATTACTGGCGT[-/GCGC]GCGCGCGCGCGCGCA | 115677 |
rs145228042 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790349 | TAGTTTCAAGGTGTA[C/T]GTCACCACAAAATAT | 115677 |
rs145318742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168788094 | ATAGTAACGATGACA[A/G]CCAGGCTTGGTGGTT | 115677 |
rs145359122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826527 | GTGTTGACCAAGTTA[C/T]TTCTACTTTAAAAGA | 115677 |
rs145416817 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844684 | GACCATCCTGGCTAA[C/G]ACGGCGAAACCCCGT | 115677 |
rs145438037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858866 | GATTCTGTTATTTAA[C/T]TCACCCTGGCTGGAC | 115677 |
rs145439677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168787327 | GGCACTGTCTCAGAA[G/T]GTGCCATGCCTGTGA | 115677 |
rs145451379 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168840089 | TCATTCCTGGGGTGC[G/T]GAGCATTCTCAATAA | 115677 |
rs145474561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797368 | TCCCAAAGTATTGAG[A/T]TAACAGGCATGAGCT | 115677 |
rs145495723 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168862123 | TAAAACCCTGTCTTA[C/G]TGTGGCAGCCTTAAG | 115677 |
rs145497455 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789800 | TGGTACAAACTGAAA[A/G]TCAGACCGAGAAACA | 115677 |
rs145519813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837530 | TAGCTAGGATAGTCT[C/T]GATCTCCTGACTTCG | 115677 |
rs145538512 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802278 | AGCATGATTAATACT[G/T]CAGGCTGAGAGGATA | 115677 |
rs145625456 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808797 | ATTGATACATGTATG[C/T]AATACAATTCCAATT | 115677 |
rs145671985 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168804022 | AGTAACCAAAGAAGA[A/T]AATTAACACCAGGGA | 115677 |
rs145692745 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168844865 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAGAAAAA | 115677 |
rs145765664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854419 | TGGGTTTCTGTCCCT[A/C]TGCCACTCATGTTTA | 115677 |
rs145769077 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168815016 | GGTATGCATTTCCAG[A/T]CCCCTTACTTAAGAG | 115677 |
rs145776458 | snp | C/T | 0.0174175 | 0.0916809 | | | GRCh38.p7 | 2:168788704 | AAGGGGAGCCAGTTT[C/T]TCACTGCTGGAAAAG | 115677 |
rs145794421 | in-del | -/TATATATGTGTG | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168839916 | ATATATATATATATA[-/TATATATGTGTG]TGTGTGTGTGTGTAT | 115677 |
rs145794908 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860504 | GGTGAAACCCCGTCT[C/G]TACTAAGAATACAAA | 115677 |
rs145866540 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168848803 | TAGGAAATGAGAAGT[C/T]GTTGTTTCATGGGTA | 115677 |
rs145872846 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808310 | TGTGGTGATGGTGGA[C/G]TGGTAGGGCCTTTCC | 115677 |
rs146009527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168800351 | GTGACAAAGGATAAA[C/T]GATACCAACCTATTT | 115677 |
rs146046051 | in-del | -/A | 0.0236746 | 0.106192 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825669 | GTAGATTCCTTTATT[-/A]GGGGGAGAGAAGAAA | 115677 |
rs146099568 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168794748 | GGTGTAAAATGGCTT[-/A]AAAAAATTAACATAT | 115677 |
rs146104426 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819083 | AGAATTAAGCACAAT[A/G]TCTTTACAAGCTTGT | 115677 |
rs146151311 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168803315 | TGTAATTTAGGAGAT[-/AAG]AAGCAACTAAAATAA | 115677 |
rs146159964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817703 | GGGCCAGAGTGAGCC[A/G]GGGCTCAGTGAGACT | 115677 |
rs146186115 | in-del | -/C | 0.0603597 | 0.1629 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168834600 | GATCTCACTGTGCTG[-/C]CCCAGGCTGGCATCA | 115677 |
rs146189468 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816308 | GACCCTGTTTAAGAC[A/G]CTTCAAAGACTCCTA | 115677 |
rs146216361 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785120 | GAAATGCTACAAAGC[A/G]AGTTTATTTTCTGTA | 115677 |
rs146254018 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168837268 | CCTTTTTACAATACA[A/T]CTTTTTTTTTTATAA | 115677 |
rs146336228 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168799766 | GAGAGGGAAAGAAAG[A/G]CATATACCAGCCACC | 115677 |
rs146384575 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168785573 | GCCAGAACACTAATG[A/C]AAGCAGTAAAATGCA | 115677 |
rs146420817 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168792731 | GTGATCCACCTGCCT[C/T]GGCCTCCGAAAGTGC | 115677 |
rs146432602 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168790350 | AGTTTCAAGGTGTAC[A/G]TCACCACAAAATATT | 115677 |
rs146438810 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | NOSTRIN | GRCh38.p7 | 2:168863997 | CTCACTGCAACCTCC[A/G]TCTCCTGGATTCAAG | 115677 |
rs146534884 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168814433 | GCTATCTAGAAATGC[A/G]CCTTGCCCTTATTTT | 115677 |
rs146560259 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168808810 | TGTAATACAATTCCA[A/G]TTAGGATCCCAACGG | 115677 |
rs146572211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168850191 | GTGCTGGGATTATAG[A/G]CATGAGCCACTGTGC | 115677 |
rs146598531 | in-del | -/AGAA | 0.0126979 | 0.078662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842095 | GGACAGTTTTTACAC[-/AGAA]AGGCAGGGGAAAGTG | 115677 |
rs146653243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168829963 | AAAAATTTTATTCAA[A/G]CTCATTAAGCTGGGT | 115677 |
rs146679390 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168826136 | ACGGTAATATAAGAC[A/G]TGTGCTTAGCAGAGT | 115677 |
rs146802123 | snp | A/C/G | 0.0135088 | 0.0812759 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168844729 | GAAAAAATTAGCCGC[A/C/G]CGTGGTGGCGGGCGC | 115677 |
rs146904781 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832209 | AGTTGGCTAGATGAC[A/G]TGTGCAGGAAATAGG | 115677 |
rs147001220 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854028 | GCACACCACCACGCC[C/T]GGCTAATTTTTTGTA | 115677 |
rs147039636 | in-del | -/ATTTAGTTGGCTAG | 0.0640965 | 0.167152 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168832190 | TTCAAGTAATTTAAA[-/ATTTAGTTGGCTAG]ATGACGTGTGCAGGA | 115677 |
rs147074957 | in-del | -/A/AAA/AAAA | 0.438105 | 0.164671 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168800910 | CTCTAAATTTCTTTT[-/A/AAA/AAAA]AAAAAAAAAACAAAA | 115677 |
rs147116355 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168795013 | TCCACCAGCCTCTCA[C/G]TTGCTGTCACAGGAA | 115677 |
rs147139526 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168810885 | ATTTATAGTTTCCAG[A/G]AAGACATTGTGGAGT | 115677 |
rs147149627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168807186 | TGAGGTAGGAGTGAG[A/T]CAACCAAAACTAAAG | 115677 |
rs147172447 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168847618 | ATGAAGAACAAATTG[C/T]CATGATGCTTGGGCC | 115677 |
rs147179847 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863129 | TTCAGTTCTCTGTTG[G/T]TTGCAAAGCCTACTT | 115677 |
rs147255349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825078 | CATTCTTAAAAATAG[C/T]AAAAAGTGACATGTT | 115677 |
rs147324058 | in-del | -/AGAT | 0.33303 | 0.235809 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788892 | CACACACAGATAAAA[-/AGAT]AGATAGATAGATAGA | 115677 |
rs147349842 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168845753 | TTTCAACTTCAGCTC[C/T]AAAAATATTTAAGAC | 115677 |
rs147359484 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842326 | TTGTTTTCTGAGTCC[C/G]AAGATGTGCCTGAAT | 115677 |
rs147465946 | snp | A/G | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833153 | TAAAATTATTGGGCT[A/G]TAATAATTTTCTCCC | 115677 |
rs147466190 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168789735 | TCAAATATATTAGGA[A/T]AAGTAGAAGTTGCTA | 115677 |
rs147488931 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168828015 | CAGAATGTAATCTCA[C/T]AGAGAAATTGAAATA | 115677 |
rs147549365 | snp | C/T | | | intron-variant | NOSTRIN | GRCh38.p7 | 2:168797079 | TTCTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 115677 |
rs147594735 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168801499 | AAGTGCTTGGATTAC[A/G]TGCATGAGCCACTGC | 115677 |
rs147604760 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168818615 | GCTTTATCTAAAATA[C/T]TGAATCTGAAATCAC | 115677 |
rs147625328 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168858025 | AATGACCCGTGGCTA[C/T]AGTTTTTATGAAATT | 115677 |
rs147726950 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NOSTRIN | GRCh38.p7 | 2:168802356 | TTACAGCTTCTCTGC[C/T]TTCTCTCAATGTTAC | 115677 |
rs147813008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168825184 | TGTGCATGCACTGTG[G/T]TAATGCTTTACTGAT | 115677 |
rs147835607 | snp | C/G | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | NOSTRIN | GRCh38.p7 | 2:168822971 | CTAATATCCCGAGAT[C/G]AGTAGGACAGTTTTC | 115677 |
rs147908517 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168786474 | ATGACCTTCCTCTAG[C/G]AACGTTAGATTGGTA | 115677 |
rs147919312 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168842754 | TATTTAAGGGTCTCA[A/G]TCTCCTCATGTGTAA | 115677 |
rs147991503 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168819965 | GAACAGGCCTGGAAG[C/T]TCGTTATGTCTGCTC | 115677 |
rs148004065 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168860396 | AACTTCCAGTCCAGG[C/T]GCAGTGGCTCATGCC | 115677 |
rs148036767 | in-del | -/TTAC | 0.0345262 | 0.126772 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168863003 | TATCTCTCCAGGCAA[-/TTAC]TTTTCTTCCTATGTG | 115677 |
rs148046535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168816273 | GCCTGTCTTTAACGC[A/G]CCTTTCACTCTGTAG | 115677 |
rs148080655 | in-del | -/AG | 0.0119091 | 0.0762411 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168817292 | CAGCCTCCTTTGCAG[-/AG]TCTTAGGGTCCTCTA | 115677 |
rs148107770 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168833318 | TGGAGAAAGAGGGCC[A/G]TGAGCTTATTTCTTT | 115677 |
rs148153153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168788790 | AAATTGTAAGTATCC[A/G]TGTATGGTTTTTAAT | 115677 |
rs148163560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NOSTRIN | GRCh38.p7 | 2:168826879 | TCATGCCTGTTTGCA[C/T]TCCTTCCCACCCAAC | 115677 |
rs148205575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NOSTRIN | GRCh38.p7 | 2:168854590 | CAACTCCCTGAACAA[C/T]TTTTTCTTCCCCTAT | 115677 |
rs148205867 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NOSTRIN, CERS6-AS1 | GRCh38.p7 | 2:168784956 | TTCAAAAAGAACCAG[C/T]ACAAGCAATTCAGTC | 115677 |