SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs769006 | snp | G/T | 0.00282885 | 0.0375023 | intron-variant | MARK1 | GRCh38.p7 | 1:220532382 | AGTACCTATCACATA[G/T]CATCTAATTGCCTga | 4139 |
rs1073460 | snp | C/T | 0.329084 | 0.237162 | intron-variant | MARK1 | GRCh38.p7 | 1:220553477 | tgctcccctgctaca[C/T]tgatgtctaaatcaa | 4139 |
rs1073461 | snp | A/G | 0.284733 | 0.247575 | intron-variant | MARK1 | GRCh38.p7 | 1:220553458 | tgtctaaatcaacaa[A/G]tatggcctcatgggg | 4139 |
rs1193030 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | MARK1 | GRCh38.p7 | 1:220621621 | TGGTTAATAAGCCTC[A/G]TAGATTTGTACCAAC | 4139 |
rs1193031 | snp | C/T | 0.305186 | 0.243833 | intron-variant | MARK1 | GRCh38.p7 | 1:220622955 | TAGCTGGTTTAATTC[C/T]TTAATTCGTCTGAAT | 4139 |
rs1193032 | snp | A/T | 0.416218 | 0.186739 | intron-variant | MARK1 | GRCh38.p7 | 1:220623356 | CTCTCTTCCCTTTCA[A/T]GTATCCATACTTCGT | 4139 |
rs1337570 | snp | C/G | 0.123105 | 0.215401 | intron-variant | MARK1 | GRCh38.p7 | 1:220602588 | CCTAGCCTAAACTCA[C/G]ATATCTAGAATTAAC | 4139 |
rs1337571 | snp | C/T | 0.287606 | 0.247155 | intron-variant | MARK1 | GRCh38.p7 | 1:220574280 | tgtaagataataaag[C/T]aggtatttggcctgt | 4139 |
rs1361092 | snp | A/C | 0.12489 | 0.216614 | intron-variant | MARK1 | GRCh38.p7 | 1:220544120 | TTTAAACCCTTTCTT[A/C]TATCTCACACCTATA | 4139 |
rs1361093 | snp | A/G | 0.123798 | 0.215808 | intron-variant | MARK1 | GRCh38.p7 | 1:220566501 | AAAAACCCCAGCAAC[A/G]GTTTGCTCTCAGTAA | 4139 |
rs1538135 | snp | C/T | 0.123452 | 0.215605 | intron-variant | MARK1 | GRCh38.p7 | 1:220590848 | CCTCTCCTTCAGCAG[C/T]TTTGGACAAGGAGAG | 4139 |
rs1856178 | snp | A/G | 0.116138 | 0.211142 | intron-variant | MARK1 | GRCh38.p7 | 1:220572402 | tacaaaaaattagcc[A/G]ggtgtggtggcacat | 4139 |
rs1890107 | snp | A/C | 0.124144 | 0.21601 | | | GRCh38.p7 | 1:220544768 | ACTTTACAGGTAGTT[A/C]ACTATAATTTGGTAC | 4139 |
rs1890108 | snp | C/T | 0.0379877 | 0.132479 | | | GRCh38.p7 | 1:220565558 | CCCGACCCCCGCTCT[C/T]CATAGGCAATCCAAG | 4139 |
rs1933001 | snp | G/T | 0.497776 | 0.0332724 | intron-variant | MARK1 | GRCh38.p7 | 1:220548079 | AAACATCCAATGAGT[G/T]GCTGCTATGTGCACA | 4139 |
rs1933002 | snp | A/G | 0.329084 | 0.237162 | intron-variant | MARK1 | GRCh38.p7 | 1:220575490 | GCTATTGATCAGGAA[A/G]GTGAGATCAGCTATC | 4139 |
rs1933003 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | MARK1 | GRCh38.p7 | 1:220575679 | TAAAATATATGCTGT[A/G]TATTCTGATTTTTTA | 4139 |
rs1933004 | snp | A/T | 0.123452 | 0.215605 | intron-variant | MARK1 | GRCh38.p7 | 1:220575761 | GCTAGGAGATCTTTT[A/T]AAAAAATCATTGAGA | 4139 |
rs1933005 | snp | A/G | 0 | 0 | intron-variant | MARK1 | GRCh38.p7 | 1:220572390 | gccaggtatggtggc[A/G]catgcctgtaatccc | 4139 |
rs1933006 | snp | A/G | | | intron-variant | MARK1 | GRCh38.p7 | 1:220572358 | gctaattgggaggct[A/G]aggcaggagaatcgc | 4139 |
rs1933008 | snp | G/T | 0.296364 | 0.245663 | intron-variant | MARK1 | GRCh38.p7 | 1:220602646 | AACTATTACCACATA[G/T]CTAGAATTAACTACT | 4139 |
rs2095669 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | MARK1 | GRCh38.p7 | 1:220535607 | aaaacataggagaag[A/G]gcttcatgatattgg | 4139 |
rs2095670 | snp | C/G | 0.124144 | 0.21601 | intron-variant | MARK1 | GRCh38.p7 | 1:220561905 | GACAAACAAAAAGCT[C/G]GCAATGTCATCCATT | 4139 |
rs2152836 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | MARK1 | GRCh38.p7 | 1:220603659 | GAATTTAAAAGAGCA[A/G]TCCAACAAAACACAC | 4139 |
rs2184936 | snp | C/T | 0.110872 | 0.20771 | intron-variant | MARK1 | GRCh38.p7 | 1:220590559 | CCAAGTATAGTCACA[C/T]TGGGCATTAGGGATT | 4139 |
rs2189942 | snp | A/C | 0.375 | 0.216506 | intron-variant | MARK1 | GRCh38.p7 | 1:220646819 | aaggattccctattt[A/C]ataaatggtgctggg | 4139 |
rs2210977 | snp | A/G | 0.137527 | 0.223271 | intron-variant | MARK1 | GRCh38.p7 | 1:220589568 | AAGAAGGAAACAAAG[A/G]CCTCTGAACAACTAG | 4139 |
rs2244448 | snp | A/G | 0.415891 | 0.18703 | intron-variant | MARK1 | GRCh38.p7 | 1:220570944 | TGGCAATTTATTTCA[A/G]TAGCTTTTTCTTTTT | 4139 |
rs2245925 | snp | A/T | 0.466939 | 0.124248 | intron-variant | MARK1 | GRCh38.p7 | 1:220533012 | GTGAACCCTTTTTTT[A/T]AAAAAAAAAAATAGA | 4139 |
rs2253641 | snp | A/C | 0.331874 | 0.236213 | intron-variant | MARK1 | GRCh38.p7 | 1:220598550 | ACTTTGGGTAAAAAT[A/C]GATTACAAAGAAGCT | 4139 |
rs2378400 | snp | A/G | 0.498253 | 0.0295011 | intron-variant | MARK1 | GRCh38.p7 | 1:220625871 | ATTTGCTGCCCAGCT[A/G]TGGTCTCCACTGAAC | 4139 |
rs2378401 | snp | G/T | 0.342582 | 0.232225 | intron-variant | MARK1 | GRCh38.p7 | 1:220629012 | AGTTGTTAGAGATCT[G/T]CCCTGGATTTCTTAT | 4139 |
rs2510808 | snp | C/T | | | intron-variant | MARK1 | GRCh38.p7 | 1:220609410 | gggatggaggaagat[C/T]taccaagcaatggaa | 4139 |
rs2589577 | snp | A/G | 0.415891 | 0.18703 | | | GRCh38.p7 | 1:220578928 | TTGAACCTGGGAGGC[A/G]GAAGTTGCAGTGAGC | 4139 |
rs2589578 | snp | A/G | 0.32885 | 0.23724 | | | GRCh38.p7 | 1:220578221 | AATGTTGAATCACAC[A/G]TAATAAACACAACAT | 4139 |
rs2589579 | snp | C/T | 0.126219 | 0.217206 | | | GRCh38.p7 | 1:220576296 | AGACTGACAGCAGGA[C/T]GATGAGAAATACATG | 4139 |
rs2589581 | snp | C/T | 0.438221 | 0.191885 | | | GRCh38.p7 | 1:220569699 | CAAACATATGTGATA[C/T]GTTAGTGTGAAATTT | 4139 |
rs2589582 | snp | A/T | 0.123798 | 0.215808 | | | GRCh38.p7 | 1:220567437 | GTTTTTCCATCCCTC[A/T]TAGGTAAAACACAAG | 4139 |
rs2589583 | snp | C/T | 0.400682 | 0.199487 | | | GRCh38.p7 | 1:220566814 | CAACACAGAAGATGT[C/T]GTCAGTGTTGAGTAA | 4139 |
rs2589584 | snp | C/T | 0.0505692 | 0.150756 | | | GRCh38.p7 | 1:220554637 | cttttttatttataa[C/T]tgttagtaaagaaac | 4139 |
rs2589586 | snp | C/T | 0.41441 | 0.188333 | | | GRCh38.p7 | 1:220551790 | CCACATGACCAGTTA[C/T]AGAAACAAGCCCTGT | 4139 |
rs2589587 | snp | A/G | 0.125528 | 0.21681 | | | GRCh38.p7 | 1:220550846 | CCCTGACTGAACTCC[A/G]ATGTGATAAATTAAA | 4139 |
rs2589588 | snp | C/T | 0.328616 | 0.237317 | | | GRCh38.p7 | 1:220546636 | ATCTTTACAAAGCAA[C/T]AATATCCCTCCTTAA | 4139 |
rs2589589 | snp | C/T | 0.401747 | 0.198678 | | | GRCh38.p7 | 1:220539755 | gcaattcaatttcaa[C/T]ggcacattagaagga | 4139 |
rs2589590 | snp | A/G | 0.112631 | 0.208878 | | | GRCh38.p7 | 1:220539463 | GAATACTGGCAAACC[A/G]AATCCAGCAGCACAT | 4139 |
rs2589591 | snp | C/T | 0.123105 | 0.215401 | | | GRCh38.p7 | 1:220600712 | TTAGCAAAAAATCAA[C/T]CAGCCAAATAATTTC | 4139 |
rs2589592 | snp | C/T | 0.256061 | 0.249927 | | | GRCh38.p7 | 1:220599555 | TCTAGGATTAAAAGG[C/T]CATTACTTTTTCAAA | 4139 |
rs2589593 | snp | A/T | 0.123452 | 0.215605 | | | GRCh38.p7 | 1:220591443 | TACATCAAATTACAG[A/T]ATACTGAAGACAACA | 4139 |
rs2589594 | snp | G/T | 0.123452 | 0.215605 | | | GRCh38.p7 | 1:220586183 | AGGTGGAAAAGGAAG[G/T]GAGGACCTTTATACC | 4139 |
rs2589595 | snp | G/T | 0.259674 | 0.249813 | | | GRCh38.p7 | 1:220586182 | GGTGGAAAAGGAAGT[G/T]AGGACCTTTATACCA | 4139 |
rs2786598 | snp | A/G | 0.412917 | 0.189626 | intron-variant, upstream-variant-2KB | MARK1 | GRCh38.p7 | 1:220548709 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCACCGCA | 4139 |
rs2786599 | snp | A/G | 0.0397512 | 0.135261 | intron-variant | MARK1 | GRCh38.p7 | 1:220615894 | AATTATTAAAAAAAC[A/G]CAATTTTCCCCAATA | 4139 |
rs2786601 | snp | A/G | 0.328616 | 0.237317 | intron-variant | MARK1 | GRCh38.p7 | 1:220545925 | ATTCGGAGTTGTGCA[A/G]GCCCAGTAAGGGAAG | 4139 |
rs2786602 | snp | A/G | 0.5 | 0 | intron-variant | MARK1 | GRCh38.p7 | 1:220586009 | CACACACACACACAC[A/G]CACGCGCGCGTGCGC | 4139 |
rs2786603 | snp | G/T | 0.123452 | 0.215605 | intron-variant | MARK1 | GRCh38.p7 | 1:220590186 | AGTTAGGCAGGGGTT[G/T]AGGGGAGTCTTGGAG | 4139 |
rs2786604 | snp | C/G | 0.32885 | 0.23724 | intron-variant | MARK1 | GRCh38.p7 | 1:220590761 | ACCATTCTTCGACAA[C/G]TGCCTATCATTTTTA | 4139 |
rs2786605 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | MARK1 | GRCh38.p7 | 1:220591977 | GACAGCAGTCTAGCA[A/G]CTTTTATCTAGTATT | 4139 |
rs2786606 | snp | A/G | 0.415727 | 0.187175 | intron-variant | MARK1 | GRCh38.p7 | 1:220592080 | TTGGACAGACTTTGA[A/G]GCAACCCCCATGATT | 4139 |
rs2786607 | snp | A/C | 0.325091 | 0.238456 | intron-variant | MARK1 | GRCh38.p7 | 1:220593881 | AGAGGCCCCCTCAGC[A/C]CTCACTCTGGATAAT | 4139 |
rs2786608 | snp | C/G | 0.124491 | 0.216211 | intron-variant | MARK1 | GRCh38.p7 | 1:220557111 | AATTTTCTTTCTATT[C/G]TGAGTTTGCCATTCC | 4139 |
rs2786609 | snp | C/T | 0.327914 | 0.237549 | intron-variant | MARK1 | GRCh38.p7 | 1:220541936 | CAAAAACCTACAAGA[C/T]GGAAAATAGTTAACA | 4139 |
rs2786610 | snp | C/T | 0.401747 | 0.198678 | intron-variant | MARK1 | GRCh38.p7 | 1:220535154 | aaatgtaaaatgctg[C/T]agctgctatgaaaaa | 4139 |
rs2786611 | snp | C/T | 0.123452 | 0.215605 | intron-variant | MARK1 | GRCh38.p7 | 1:220582981 | ACTTGATCTGCTTTT[C/T]CTTCAGAACTTCTAA | 4139 |
rs2786612 | snp | C/G | 0.287606 | 0.247155 | intron-variant | MARK1 | GRCh38.p7 | 1:220582908 | ACAATCACACACACA[C/G]TGTACTGGCTACATT | 4139 |
rs2786613 | snp | C/T | 0.32885 | 0.23724 | intron-variant, upstream-variant-2KB | MARK1 | GRCh38.p7 | 1:220578759 | ACAAACCATTATTCC[C/T]ATAAAGGTGTTATCG | 4139 |
rs2786615 | snp | A/G | 0.123798 | 0.215808 | intron-variant | MARK1 | GRCh38.p7 | 1:220568638 | AGGGGACTGGGAAAC[A/G]GGAGTATAGGGAACA | 4139 |
rs2786616 | snp | A/T | 0.408017 | 0.193729 | intron-variant | MARK1 | GRCh38.p7 | 1:220566820 | AGCATTCAACACAGA[A/T]GATGTTGTCAGTGTT | 4139 |
rs2786617 | snp | C/T | 0.405255 | 0.195948 | intron-variant | MARK1 | GRCh38.p7 | 1:220562986 | ATGCAGGAAGAGGAC[C/T]GATATCAATATGTAC | 4139 |
rs2786618 | snp | A/G | 0.124144 | 0.21601 | intron-variant | MARK1 | GRCh38.p7 | 1:220559369 | tccatcattccactg[A/G]gactagccttgtcaa | 4139 |
rs2786619 | snp | C/G | 0.328382 | 0.237395 | intron-variant | MARK1 | GRCh38.p7 | 1:220551448 | GGCCAAGCTGACAAG[C/G]AGTGGGTTTTAATGA | 4139 |
rs2815776 | snp | C/T | | | intron-variant | MARK1 | GRCh38.p7 | 1:220646920 | caaatggattaaaga[C/T]ttaaatgtaaaaccc | 4139 |
rs2889894 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | MARK1 | GRCh38.p7 | 1:220617047 | CCATCCAGACATTTT[G/T]AGAGAGACTGAAAAA | 4139 |
rs2889895 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | MARK1 | GRCh38.p7 | 1:220654788 | TAGTGCTTGATTACT[A/G]ATTGTGCATTAAGCA | 4139 |
rs2889928 | snp | C/T | 0.32885 | 0.23724 | intron-variant | MARK1 | GRCh38.p7 | 1:220558832 | CTCAATGGAAATGTA[C/T]AGAGTCGTATACTCT | 4139 |
rs2993209 | snp | A/G | 0.329317 | 0.237084 | intron-variant | MARK1 | GRCh38.p7 | 1:220611646 | tctgcagctcccagc[A/G]tgatcatcccagaag | 4139 |
rs2994526 | snp | A/T | 0.123105 | 0.215401 | intron-variant | MARK1 | GRCh38.p7 | 1:220611207 | ccaccgcagcccaac[A/T]aggcctactgcctct | 4139 |
rs2994527 | snp | A/G | 0.32885 | 0.23724 | intron-variant | MARK1 | GRCh38.p7 | 1:220609467 | gtgctgtattcagga[A/G]acccatctcatgtgc | 4139 |
rs3010236 | snp | A/G | 0.123452 | 0.215605 | intron-variant | MARK1 | GRCh38.p7 | 1:220587666 | tgagccaccgtgccc[A/G]gccTTgttcatttat | 4139 |
rs3062186 | in-del | -/A/TA/TATAT | 0.000232748 | 0.0107852 | intron-variant | MARK1 | GRCh38.p7 | 1:220598418 | ATATATATATATATA[-/A/TA/TATAT]ATTAGCGATGAAGTG | 4139 |
rs3737296 | snp | A/G | 0.360297 | 0.224403 | intron-variant | MARK1 | GRCh38.p7 | 1:220652181 | CATCTCATTTTGTTC[A/G]TTAAGAGTTTCTAAA | 4139 |
rs3737297 | snp | C/T | 0.15792 | 0.232425 | intron-variant | MARK1 | GRCh38.p7 | 1:220652201 | GAGTTTCTAAAAATA[C/T]AGCACCATGTGAAAA | 4139 |
rs3737298 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MARK1 | GRCh38.p7 | 1:220652366 | TTTTCTAGAGGAATT[G/T]TTTTAAGGATTTGAT | 4139 |
rs3753874 | snp | A/G | 0.495818 | 0.0455352 | upstream-variant-2KB | MARK1 | GRCh38.p7 | 1:220527843 | ACAAACAAACAAACA[A/G]ACAAAAACAGAAAGA | 4139 |
rs3753875 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | MARK1 | GRCh38.p7 | 1:220627062 | TCCAGTATGACTAAC[A/C]AGAACACGAATGGTA | 4139 |
rs3753876 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | MARK1 | GRCh38.p7 | 1:220650479 | TCTAAATTAGAGAGA[C/G]GCAGGGGATAATCTT | 4139 |
rs3753877 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | MARK1 | GRCh38.p7 | 1:220657371 | ATTTGCTAACTACAA[A/G]GTTAATGTATATATT | 4139 |
rs3767319 | snp | A/G | 0.498459 | 0.0277128 | intron-variant | MARK1 | GRCh38.p7 | 1:220600281 | GATTGTTCACATATG[A/G]CAGATTCTCAATATA | 4139 |
rs3767320 | snp | A/G | 0.498611 | 0.0263212 | intron-variant | MARK1 | GRCh38.p7 | 1:220600292 | TATGACAGATTCTCA[A/G]TATACATACATTTCC | 4139 |
rs3767321 | snp | A/C | 0.499527 | 0.0153681 | intron-variant | MARK1 | GRCh38.p7 | 1:220623220 | GCTCTCTCCTGTCAC[A/C]CAGTACCTCCATTTT | 4139 |
rs3767323 | snp | A/C | 0.499464 | 0.016365 | intron-variant | MARK1 | GRCh38.p7 | 1:220627528 | TTATGCTTTCTATTT[A/C]TCTGTGTATTTATAG | 4139 |
rs3820346 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | MARK1 | GRCh38.p7 | 1:220526729 | CAAAGGGATCTTGTT[G/T]TTTTTTTTTTTTTCA | 4139 |
rs3820347 | snp | A/G | 0.498589 | 0.02652 | intron-variant | MARK1 | GRCh38.p7 | 1:220638843 | AGGAGTTTCTAAAGT[A/G]AAATTAATCATCTCC | 4139 |
rs3831285 | in-del | -/G | 0.498459 | 0.0277128 | intron-variant, utr-variant-3-prime | MARK1 | GRCh38.p7 | 1:220582572 | TCACTCAATTTGCCA[-/G]AGTAACCCACAACTA | 4139 |
rs3835572 | in-del | -/CAAA | | | upstream-variant-2KB | MARK1 | GRCh38.p7 | 1:220527824 | AAACAAACAAACAAA[-/CAAA]AACAGAAAGAAAGAA | 4139 |
rs3835573 | in-del | -/T | 0.158962 | 0.232835 | intron-variant | MARK1 | GRCh38.p7 | 1:220656789 | ATTCAGATAGAAAAA[-/T]TTTTTTTTTCATAAT | 4139 |
rs3849285 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | MARK1 | GRCh38.p7 | 1:220626264 | ATATTGACATTGATA[A/T]TCACCACGGCGATGG | 4139 |
rs3849286 | snp | A/C | 0.444444 | 0.157135 | intron-variant | MARK1 | GRCh38.p7 | 1:220649239 | GAAATCCTGTCCCCC[A/C]AAAAAAAAAAAGACT | 4139 |
rs4011894 | snp | A/G | 0.325091 | 0.238456 | intron-variant | MARK1 | GRCh38.p7 | 1:220613960 | TTTTTGGTTTGGTTT[A/G]GTTTTGTGGGGTTTA | 4139 |
rs4338357 | snp | C/G | 0.498693 | 0.0255257 | intron-variant | MARK1 | GRCh38.p7 | 1:220638870 | CTCCTCTTCCCTATC[C/G]ATTTCCTTTTAGTCT | 4139 |
rs4481855 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | MARK1 | GRCh38.p7 | 1:220534642 | ttttcatcttgtgtg[A/G]ctgaaacagtgtaca | 4139 |