SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8907 | snp | A/G | 0.183946 | 0.241116 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260914 | GTTGCTGCGGCGTCT[A/G]CGAGGCCCGAGGGTG | 51096 |
rs14180 | snp | C/T | 0.236407 | 0.24963 | synonymous-codon, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51260896 | CGAGAACGACGAGGA[C/T]GCGTTGCTGCGGCGT | 51096 |
rs917654 | snp | C/G | 0.437401 | 0.165472 | intron-variant | UTP18 | GRCh38.p7 | 17:51294144 | TACAGTTAATAAATT[C/G]TAGTCTGTTTATCTT | 51096 |
rs1015709 | snp | C/T | 0.264084 | 0.249603 | intron-variant | UTP18 | GRCh38.p7 | 17:51279084 | AATATTGTAACTTAG[C/T]AACTTAAAATTTTAA | 51096 |
rs1019195 | snp | A/G | 0.437118 | 0.165792 | intron-variant | UTP18 | GRCh38.p7 | 17:51278160 | ACTTTGATCCTTTCC[A/G]AGTAGATCCTTGGTT | 51096 |
rs2318787 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51270174 | TTTTTCCCCTTCTTC[C/T]CTTTTCTTTAAGAAC | 51096 |
rs2318788 | snp | C/T | 0.43655 | 0.16643 | intron-variant | UTP18 | GRCh38.p7 | 17:51270259 | ACGGTTTGAAACATA[C/T]AGATTATCTTCTTTT | 51096 |
rs2318789 | snp | A/C | 0.496074 | 0.044618 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51273441 | TTCTCTTCCAAGAGG[A/C]ATCTTGAAGGTGAGA | 51096 |
rs3217081 | in-del | -/AG | 0.488846 | 0.0738428 | intron-variant | UTP18 | GRCh38.p7 | 17:51276141 | TCTCACAGAAGTGAC[-/AG]AGTTCATTTACTTGG | 51096 |
rs3217082 | in-del | -/CA | | | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51297977 | CCAACACACACACAC[-/CA]AAACTTGGATGCATT | 51096 |
rs3786007 | snp | A/G | 0.437542 | 0.165312 | intron-variant | UTP18 | GRCh38.p7 | 17:51274377 | ATCTGTCATACTAAC[A/G]GGCAGTACTTTAGTT | 51096 |
rs3786008 | snp | G/T | 0.110167 | 0.207236 | intron-variant | UTP18 | GRCh38.p7 | 17:51274920 | AGTTACCACATGGCC[G/T]GGCGCAGTGGCTCAC | 51096 |
rs3837855 | in-del | -/T | 0.437401 | 0.165472 | intron-variant | UTP18 | GRCh38.p7 | 17:51275239 | CCATAAAAATTTAAC[-/T]TTGGTGGTTACAAAC | 51096 |
rs4448992 | snp | A/G | 0.437118 | 0.165792 | intron-variant | UTP18 | GRCh38.p7 | 17:51270473 | GATTCCTGTAATTTT[A/G]GGTATGGTTATGCTA | 51096 |
rs4793690 | snp | A/T | 0.486855 | 0.0799975 | intron-variant | UTP18 | GRCh38.p7 | 17:51264049 | TTTTTTTTAATTATT[A/T]TTTTTGAAACAGAGT | 51096 |
rs4793691 | snp | G/T | 0.488905 | 0.0736498 | intron-variant | UTP18 | GRCh38.p7 | 17:51283299 | tcagcctcctgggta[G/T]ctgggattacaggca | 51096 |
rs4793692 | snp | A/C | 0.488905 | 0.0736498 | intron-variant | UTP18 | GRCh38.p7 | 17:51283542 | TTGTTACATGTAAAG[A/C]ATAATTTGAGATAAA | 51096 |
rs4794217 | snp | G/T | 0.493925 | 0.054776 | intron-variant | UTP18 | GRCh38.p7 | 17:51268014 | TGTTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTGA | 51096 |
rs4794218 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | UTP18 | GRCh38.p7 | 17:51270280 | ATCTTCTTTTTCTCT[C/T]ATTTGGGAAGCCTCT | 51096 |
rs4794219 | snp | G/T | 0.437259 | 0.165632 | intron-variant | UTP18 | GRCh38.p7 | 17:51279512 | TTGTTTTTTGTTTTT[G/T]TTTTTGACTCACAAA | 51096 |
rs4794220 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | UTP18 | GRCh38.p7 | 17:51286186 | GCTATTACTGAAAAC[A/G]TTGGTTATTACACTG | 51096 |
rs4794221 | snp | A/T | 0.440609 | 0.161766 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286828 | TTATAAGTAGTTTTT[A/T]AATTTTTTTTATTAT | 51096 |
rs5820850 | in-del | -/T | 0.375 | 0.216506 | intron-variant | UTP18 | GRCh38.p7 | 17:51293503 | AAACATGAGTTGTTG[-/T]TTTTTTTTTTTTTAA | 51096 |
rs6504702 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | UTP18 | GRCh38.p7 | 17:51276948 | TACCTTCTGTTAAGC[C/T]TTTTTATGAAGGCCT | 51096 |
rs6504703 | snp | A/G | 0.43598 | 0.167067 | intron-variant | UTP18 | GRCh38.p7 | 17:51283026 | ggcgcataccgccat[A/G]cccagctaatttttt | 51096 |
rs6504704 | snp | A/G | 0.436692 | 0.166271 | intron-variant | UTP18 | GRCh38.p7 | 17:51283030 | cataccgccataccc[A/G]gctaattttttgtat | 51096 |
rs7210107 | snp | C/G | 0.490119 | 0.0695896 | intron-variant | UTP18 | GRCh38.p7 | 17:51284616 | TGCTTCAGATTTTTG[C/G]TTCAATAATTTATCT | 51096 |
rs7210300 | snp | C/G | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51284702 | TTTTTTCCTGTAAAC[C/G]TAAAGGTACTGTCTA | 51096 |
rs7211731 | snp | A/G | 0.184521 | 0.241273 | intron-variant | UTP18 | GRCh38.p7 | 17:51263623 | AGTAGCTAAGAGAAT[A/G]CAGTGTTTGAAGTCA | 51096 |
rs7213331 | snp | A/G | 0.247053 | 0.249983 | intron-variant | UTP18 | GRCh38.p7 | 17:51272980 | TTCATGTGAGTTGTT[A/G]AACTAGATCAGTAGC | 51096 |
rs7215691 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | UTP18 | GRCh38.p7 | 17:51286376 | ACCAAACACAATTGA[A/G]CCATGAAATGATTTC | 51096 |
rs7217151 | snp | C/T | 0.436408 | 0.16659 | intron-variant | UTP18 | GRCh38.p7 | 17:51264902 | tggccaggctggtct[C/T]gaactgttgacctca | 51096 |
rs7502980 | snp | A/G | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51273582 | TCATTTTGCCCTGGT[A/G]AATACTTATGTTATT | 51096 |
rs8064307 | snp | C/G | 0.488846 | 0.0738428 | intron-variant | UTP18 | GRCh38.p7 | 17:51271880 | accattttggtcagg[C/G]tggtctcgaactcct | 51096 |
rs8067441 | snp | A/G | 0.0120287 | 0.0766138 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51275985 | TAATGCTGTATCACT[A/G]TTTCAGGTATGCATC | 51096 |
rs8069804 | snp | A/G | 0.261056 | 0.249755 | upstream-variant-2KB, utr-variant-5-prime | UTP18, MBTD1 | GRCh38.p7 | 17:51260442 | GGGAGTTACGTAGAG[A/G]GAGGGAGTGCTGGTC | 51096 |
rs8070746 | snp | A/G | 0.490343 | 0.0688145 | intron-variant | UTP18 | GRCh38.p7 | 17:51268316 | caggcgtgagccatg[A/G]cgcccggccCAGGTA | 51096 |
rs8071800 | snp | C/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51268268 | cctgacctcgtgatc[C/T]gcccgccttggcctc | 51096 |
rs8076189 | snp | A/G | 0.437259 | 0.165632 | intron-variant | UTP18 | GRCh38.p7 | 17:51270640 | AGGTTGGTTCTTCCA[A/G]AGTTGCCTAAGATGT | 51096 |
rs8076318 | snp | C/T | 0.43555 | 0.167544 | intron-variant | UTP18 | GRCh38.p7 | 17:51268314 | tacaggcgtgagcca[C/T]ggcgcccggccCAGG | 51096 |
rs8076463 | snp | C/T | 0.184203 | 0.241186 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261736 | GGCGTGTGTAGAGGC[C/T]TGTGAAATTTTAGAT | 51096 |
rs8077559 | snp | G/T | 0.247337 | 0.249986 | intron-variant | UTP18 | GRCh38.p7 | 17:51270308 | TCTTTCCATGTTTGT[G/T]TTTTAATATGTTAAA | 51096 |
rs8078941 | snp | A/G | 0.489024 | 0.0732638 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287073 | CCTCTATATGGGGCA[A/G]GAAAAACTGCGCAGA | 51096 |
rs8078958 | snp | A/C | 0.437542 | 0.165312 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51287124 | GTGAAGCCAGTCTTC[A/C]TTGCCCTCTCTTTTT | 51096 |
rs8080145 | snp | C/T | 0.43655 | 0.16643 | intron-variant | UTP18 | GRCh38.p7 | 17:51268536 | CATAGTCCTGATATC[C/T]GGGATGTGTTGATAT | 51096 |
rs8082304 | snp | A/G | 0.184203 | 0.241186 | intron-variant | UTP18 | GRCh38.p7 | 17:51272291 | tttagtagagacggg[A/G]tttctccatgttggc | 51096 |
rs9889715 | snp | C/T | 0.490063 | 0.0697833 | intron-variant | UTP18 | GRCh38.p7 | 17:51273797 | TAATTCTAGGAATCC[C/T]GTTTGGTTTATCTTC | 51096 |
rs9889777 | snp | A/C | 0.429388 | 0.174127 | upstream-variant-2KB, intron-variant | UTP18, MBTD1 | GRCh38.p7 | 17:51259432 | TTCCCCTGCAAAGCA[A/C]CGAAACTGTGCTCCC | 51096 |
rs9891795 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | UTP18 | GRCh38.p7 | 17:51283148 | tgctaggattacagg[C/T]gtgagccaccgcgcc | 51096 |
rs9893020 | snp | A/G | 0.248755 | 0.249997 | intron-variant | UTP18 | GRCh38.p7 | 17:51291749 | atctcaaaaaaaaaa[A/G]aaaagaaaagaaaag | 51096 |
rs9893889 | snp | C/T | 0.192088 | 0.2432 | intron-variant | UTP18 | GRCh38.p7 | 17:51285924 | ATGCTGGCGCTACCT[C/T]ATATCATTGTATTTT | 51096 |
rs9894562 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | UTP18 | GRCh38.p7 | 17:51267382 | gttaggcattttaaa[A/G]tgtaaatttggtggc | 51096 |
rs9896351 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | UTP18 | GRCh38.p7 | 17:51283415 | tcaggtgatctgccc[A/G]ccttggcctcccaaa | 51096 |
rs9897204 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | UTP18 | GRCh38.p7 | 17:51267800 | GGTGatggggttcat[C/T]ttgcttatatccctt | 51096 |
rs9901084 | snp | C/T | 0.489722 | 0.0709447 | intron-variant | UTP18 | GRCh38.p7 | 17:51264690 | TTTAGTCATTGTCTT[C/T]TTTTTTTTTTTTTTG | 51096 |
rs9903174 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | UTP18 | GRCh38.p7 | 17:51280536 | TTTAAATTTTAggcc[A/G]ggcgcggtggctcac | 51096 |
rs9904690 | snp | C/T | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | UTP18, MBTD1 | GRCh38.p7 | 17:51261463 | TCTGGCAATGGCAAA[C/T]CCTGCGTGATTGATC | 51096 |
rs9906420 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269093 | ggagtttaagaccag[A/C]ccgggtgacatggcg | 51096 |
rs9906442 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269131 | atctctacaaaaaat[A/C]caaaaattagccagg | 51096 |
rs9906719 | snp | A/C | 0.00956916 | 0.0685055 | intron-variant | UTP18 | GRCh38.p7 | 17:51269255 | taagtgataagtgcc[A/C]ccgtactccagcctg | 51096 |
rs9908910 | snp | C/T | 0.190205 | 0.242744 | intron-variant | UTP18 | GRCh38.p7 | 17:51265760 | gtagagatggtgttt[C/T]accacgttggccaag | 51096 |
rs9911123 | snp | A/G | 0.154865 | 0.231191 | intron-variant | UTP18 | GRCh38.p7 | 17:51266297 | TAAGTGTCTTTTTTC[A/G]TATGATTTACCAAGA | 51096 |
rs9911355 | snp | A/G | 0.437259 | 0.165632 | intron-variant | UTP18 | GRCh38.p7 | 17:51269532 | CCTCTCACATCATGT[A/G]GGAGCTCCTTCCTTA | 51096 |
rs10514982 | snp | G/T | 0.253824 | 0.249971 | intron-variant | UTP18 | GRCh38.p7 | 17:51271203 | TGGCTTGATGTCTTC[G/T]GTAAGTTTTGGAAAT | 51096 |
rs10604907 | in-del | -/CT | 0.437824 | 0.164991 | intron-variant | UTP18 | GRCh38.p7 | 17:51267960 | AAAAAATTAAAACAA[-/CT]CTCTTTGCCCTCTTC | 51096 |
rs10695281 | in-del | -/TT | 0 | 0 | intron-variant | UTP18 | GRCh38.p7 | 17:51265583 | TTTTTTTTTTTTTTT[-/TT]GAGACAGTCTCACTC | 51096 |
rs10853118 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | UTP18 | GRCh38.p7 | 17:51269595 | TTATGACCACCTCCT[C/T]TGTCCCCTTTCTTCC | 51096 |
rs11079951 | snp | C/T | 0.48818 | 0.0759629 | intron-variant | UTP18 | GRCh38.p7 | 17:51265326 | TAGAGTGTAGTGGTG[C/T]GATCTTGGCTCACTG | 51096 |
rs11079952 | snp | C/G | 0.488965 | 0.0734569 | intron-variant | UTP18 | GRCh38.p7 | 17:51268393 | TTTCCAGAGTGAAGT[C/G]ATTCTGTTTTATTCA | 51096 |
rs11079953 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | UTP18 | GRCh38.p7 | 17:51269096 | GTTTAAGACCAGACC[A/G]GGTGACATGGCGAAA | 51096 |
rs11397806 | in-del | -/C/CC | 0.5 | 0.000399361 | intron-variant, downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51286978 | CCCCCTTCCCCCCCC[-/C/CC]GACCCACAGGCCCCG | 51096 |
rs11657473 | snp | A/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51269315 | aaaaaaaaaaaaaaa[A/C]aaaaaaaaaAACCAA | 51096 |
rs11867403 | snp | G/T | 0.482384 | 0.0921818 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298290 | TCTGGCCTTATTACT[G/T]CAAATCTTTGTCATT | 51096 |
rs12453696 | snp | A/G | 0.245346 | 0.249957 | downstream-variant-500B | UTP18 | GRCh38.p7 | 17:51298324 | ATTTGAAGAGGAGCC[A/G]TAGTAAACCTGGTAG | 51096 |
rs12937109 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274758 | gcccagcGACATAGG[G/T]CTCTTTTCTTATTAC | 51096 |
rs12937608 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274881 | TTAGCTCTTTACGGG[G/T]GAATTCACCTCCATT | 51096 |
rs12937624 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274902 | CACCTCCATTAAAAA[A/T]GTAGTTACCACATgg | 51096 |
rs12940196 | snp | C/G | 0.496036 | 0.0443428 | intron-variant | UTP18 | GRCh38.p7 | 17:51293869 | CATGAGCTCCCAGTT[C/G]TTACACTTTAAAGTT | 51096 |
rs12941969 | snp | A/C | 0 | 0 | intron-variant, missense | UTP18 | GRCh38.p7 | 17:51286563 | GAAAGGCAAGTAGAA[A/C]TAGGCTGTGGAGCTT | 51096 |
rs12943945 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274756 | gcgcccagcGACATA[A/G]GTCTCTTTTCTTATT | 51096 |
rs12947643 | snp | A/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51274909 | ATTAAAAATGTAGTT[A/T]CCACATggccgggcg | 51096 |
rs12948421 | snp | A/G | 0.488545 | 0.074807 | intron-variant | UTP18 | GRCh38.p7 | 17:51290776 | TAAAAGCCAAATCAC[A/G]GTTTTTAAATGGTAG | 51096 |
rs12951150 | snp | C/G | 0.488118 | 0.0761554 | intron-variant | UTP18 | GRCh38.p7 | 17:51264768 | GCTCACTGCAACCTC[C/G]GCCTCCCAGGTTCAA | 51096 |
rs16949739 | snp | A/G | 0.184521 | 0.241273 | intron-variant | UTP18 | GRCh38.p7 | 17:51269688 | ATAATTCTATTAGAA[A/G]AGACAATCTGTTACT | 51096 |
rs16949746 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51276721 | GTATCTGCTCTTGGA[G/T]AGGGTATCCCAGTTT | 51096 |
rs16949750 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51279351 | TATGAACCTTTCAGT[C/T]ATGGAAAAAGAGACA | 51096 |
rs16949752 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | UTP18 | GRCh38.p7 | 17:51280214 | TCTCCAAGTAGAGGA[A/G]CACAGGTGGGACTTG | 51096 |
rs16949753 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | UTP18 | GRCh38.p7 | 17:51282067 | GTTAACTCTTACTGT[C/T]TATCCCAAAGGACCA | 51096 |
rs16949758 | snp | A/G | 0.0433465 | 0.140692 | intron-variant, synonymous-codon | UTP18 | GRCh38.p7 | 17:51286675 | TTCCTACCCATACCC[A/G]TGCCAACCCTGTAGC | 51096 |
rs17575641 | snp | A/G | 0.267908 | 0.249358 | intron-variant | UTP18 | GRCh38.p7 | 17:51293134 | TGATCAGATTTTAGT[A/G]TTCTTTACTGTGGTC | 51096 |
rs28379319 | snp | C/T | 0.021895 | 0.102314 | synonymous-codon | UTP18 | GRCh38.p7 | 17:51263276 | TTGTCTGCTGTAGGT[C/T]CAAGAACATGAAGAC | 51096 |
rs28459876 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | UTP18 | GRCh38.p7 | 17:51273906 | TTTACTTCTACTTTA[C/T]CTCTTTTTAAATCAT | 51096 |
rs34049859 | snp | A/G | | | intron-variant | UTP18 | GRCh38.p7 | 17:51276329 | GTATGACTTCAGTGT[A/G]CAAGGAACCATAATA | 51096 |
rs34103760 | in-del | -/TT/TTT | 0.479663 | 0.0987666 | intron-variant | UTP18 | GRCh38.p7 | 17:51283617 | TTTTTTTTTTTTTTT[-/TT/TTT]GGAGACAGCATTGCT | 51096 |
rs34113761 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51291595 | AAAAATTAGCTGGGC[-/C]GTGGTAGCCCACACC | 51096 |
rs34120435 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51296741 | TTTCATAGACCCCCC[-/C]ATGTGAAACTTTGGA | 51096 |
rs34207677 | snp | G/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51262512 | CCAGACTGGAGTGTA[G/T]CGGCACCTATTAGTC | 51096 |
rs34301015 | snp | C/T | 0.487995 | 0.0765403 | intron-variant | UTP18 | GRCh38.p7 | 17:51262740 | AATTTTCTGTAGAGA[C/T]GAGATCTCCCTATGT | 51096 |
rs34328363 | in-del | -/T | | | intron-variant | UTP18 | GRCh38.p7 | 17:51281215 | TTTCTTTTTAGCTAG[-/T]AAAATCAGATCTATT | 51096 |
rs34329392 | in-del | -/C | | | intron-variant | UTP18 | GRCh38.p7 | 17:51294495 | AGAATGATGGTTTCC[-/C]AGTTTCATCCATGTC | 51096 |