SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs448 | snp | C/T | 0.44546 | 0.155869 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96092968 | TAAAGACCACATAAC[C/T]TTCACCTGTTAGTGT | 1780 |
rs449 | snp | A/G | 0.16618 | 0.23553 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96092950 | CACCTGTTAGTGTGG[A/G]GCAATCAAGACTCAC | 1780 |
rs450 | snp | G/T | 0.447421 | 0.153379 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96092922 | CACCCCTTTGAGAAA[G/T]GCCAGCATTCCATGA | 1780 |
rs451 | snp | A/G | 0.382085 | 0.212258 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96092746 | TCATTTTAGCCTCCC[A/G]GAGCCCCACCACCCA | 1780 |
rs452 | snp | G/T | 0.445328 | 0.156035 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96092698 | TCGGACCATGTCAGG[G/T]ATCAGTCCCCTCCTC | 1780 |
rs42059 | snp | A/G | 0.450609 | 0.149185 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96096252 | AATTTCCCACCACAC[A/G]GAGCCAAATGATTAG | 1780 |
rs42060 | snp | C/T | 0.181978 | 0.240568 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96093546 | TTTTCATGCCAAAAG[C/T]ACTTGAGGCTCAGAT | 1780 |
rs42061 | snp | C/T | 0.180702 | 0.240204 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96093355 | CTCAAGTCCTGTTCT[C/T]ATCTTGGTTGCTGGC | 1780 |
rs42064 | snp | A/T | 0.499234 | 0.0195537 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96089945 | TGCTACACAAGCTCA[A/T]CTGTCATATTAGCTA | 1780 |
rs42065 | snp | C/T | 0.444 | 0.157683 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96089267 | TTTTGTACAATTCTG[C/T]GGATGTGGTCTTCCA | 1780 |
rs42066 | snp | A/G | 0.185788 | 0.241613 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96089012 | AGAAACTATTGGTTG[A/G]CTATTAGGAGAAAGA | 1780 |
rs42067 | snp | G/T | 0.340559 | 0.233022 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96087313 | TTAAAACTGGCTGAT[G/T]GCAAATGCAGTTCTT | 1780 |
rs42068 | snp | C/T | 0.449473 | 0.150701 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96087258 | TTAACCTCCCAAATC[C/T]AAGTTTAACTTTTCA | 1780 |
rs42069 | snp | A/G | 0.339429 | 0.233457 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96086480 | GGATAAGATTTGTCC[A/G]TCTCTCAAACCATGG | 1780 |
rs42070 | snp | A/T | 0.445592 | 0.155704 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96086456 | ACCATGGTTTTTAAG[A/T]TTCCATTTTATTCTT | 1780 |
rs42071 | snp | A/C | 0.332337 | 0.236052 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96085724 | ATGGTGCATGCAACC[A/C]CTGTCTATGTAAGTA | 1780 |
rs42072 | snp | C/T | 0.183568 | 0.241012 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96084585 | AAATACAAAAATTTG[C/T]TGGGTGTTGTGGCAT | 1780 |
rs42073 | snp | C/T | 0.449345 | 0.150869 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96084568 | GGGTGTTGTGGCATG[C/T]GCCTGTAATCCCAGA | 1780 |
rs42074 | snp | A/G | 0.32955 | 0.237006 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96084539 | GATACTTAGGAGGCT[A/G]AGGCAGGAGAATTGC | 1780 |
rs42075 | snp | C/T | 0.184203 | 0.241186 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96084516 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAAGTGT | 1780 |
rs42076 | snp | C/T | 0.330947 | 0.236533 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96084465 | GCAAGAGCAAAACTC[C/T]GTCTCAAAAAAAAAA | 1780 |
rs42077 | snp | A/G | 0.183568 | 0.241012 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96083494 | CCTATAGTAATCACA[A/G]TAATGGCAGCATTTG | 1780 |
rs42078 | snp | C/G | 0.183568 | 0.241012 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96082296 | AAAGAGAGAGAAAAG[C/G]CTTTTTTTTTTTTTA | 1780 |
rs42079 | snp | C/T | 0.447162 | 0.153712 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96081989 | TTGGAACTCAGCTTG[C/T]GGTATCAGGAGTAGT | 1780 |
rs42080 | snp | C/T | 0.190833 | 0.242898 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96081818 | ACCGTCTAGCTTGTT[C/T]CAACATAATCAACTA | 1780 |
rs42081 | snp | A/G | 0.185472 | 0.241529 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96080925 | CTGCCACCATGCCCG[A/G]CTAATTTTTGTATTT | 1780 |
rs42082 | snp | G/T | 0.49979 | 0.0102493 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96080354 | TTGGAACCTGCCAAA[G/T]GGTTCACAACAGAAT | 1780 |
rs42083 | snp | A/G | 0.493568 | 0.0563433 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96080290 | AATTTACAATAATAC[A/G]TTTAACTGGATGAGT | 1780 |
rs42084 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96080011 | TAGGGTCATAGTTTA[C/T]GGACAGATGGAGAGA | 1780 |
rs81018 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96000514 | CTTTTCCGAAAGGCA[C/T]AAAGTAGCAATGTTG | 1780 |
rs143310 | snp | C/T | 0.254944 | 0.249951 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95950163 | AAGAAATGTGAAAAA[C/T]GAGCCTTGCGAAAAC | 1780 |
rs172762 | snp | A/G | 0.442385 | 0.15965 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95940292 | acaaagatactcctc[A/G]agaagagcaactcca | 1780 |
rs182650 | snp | G/T | 0.362313 | 0.223351 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96003736 | TCCACTCTTGGTGGG[G/T]ACTCATCTGGCCTGG | 1780 |
rs184381 | snp | C/T | 0.439224 | 0.163383 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95911027 | TAAAAATGTGACACC[C/T]TCAAAGCATAGCTTT | 1780 |
rs188848 | snp | C/G | 0.397994 | 0.201489 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95919429 | AAACAGAGTTAATCA[C/G]GTTTGATGTTTGGTT | 1780 |
rs223108 | snp | A/T | 0.236144 | 0.249616 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95971982 | CTGCCAGAGCCCTTG[A/T]TGCTCTGCTCCTGAC | 1780 |
rs319289 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96024590 | AAGCATTATTAAATG[A/G]AGACTAATAAAATGC | 1780 |
rs319290 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96024567 | TAAAATGCAGACAAA[C/T]GAAATTAACTGGAAA | 1780 |
rs319291 | snp | A/G | 0.437824 | 0.164991 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95940032 | aaggagaaataaaat[A/G]ctttacagacaagca | 1780 |
rs319292 | snp | A/C | 0.458315 | 0.13822 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95939613 | aaggcaggggttgca[A/C]tcctagtctctgata | 1780 |
rs319293 | snp | G/T | 0.41408 | 0.188621 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95939556 | aaaagagacaaagaa[G/T]gccattacataatgg | 1780 |
rs319294 | snp | G/T | 0.268995 | 0.249277 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95939042 | gggtgcataatgaaa[G/T]gaaggcagaaataaa | 1780 |
rs319295 | snp | C/T | 0.280256 | 0.248162 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95938676 | ctcattacatcttta[C/T]aacagacctatgaga | 1780 |
rs319296 | snp | C/T | 0.424659 | 0.17887 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95936188 | ACAAATACACATATT[C/T]CATTAATTTCTCAGT | 1780 |
rs319297 | snp | C/T | 0.25801 | 0.249872 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95935843 | acatgtttgcatgta[C/T]tggttggccatttgt | 1780 |
rs319298 | snp | C/G | 0.453453 | 0.145282 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95908878 | TCTTTTGTTTCTTTA[C/G]AGGCCAAGATCACAT | 1780 |
rs319299 | snp | A/G | 0.459687 | 0.136129 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95903058 | TGAGGCTGCACCACT[A/G]GGCTATCTCATGCCC | 1780 |
rs319300 | snp | A/T | 0.264358 | 0.249587 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95903007 | CAACTAAATTAATGA[A/T]GTTCCTGAGTCAGCC | 1780 |
rs319301 | snp | A/G | 0.440884 | 0.161442 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95975239 | TAGCAAAACTTGAAA[A/G]CTAATAAAGCCAGTA | 1780 |
rs319302 | snp | A/G | 0.239614 | 0.249784 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95974735 | TGGATTATTTTATTT[A/G]TCAGGTATTCTACAA | 1780 |
rs319303 | snp | C/T | 0.441432 | 0.160792 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95974462 | TCCTTCCTTAAAACA[C/T]GTTGTTGTAAGAATA | 1780 |
rs319304 | snp | C/T | 0.44755 | 0.153212 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95974420 | TAACCAATACAAAAT[C/T]GCTTTTTAAACCATC | 1780 |
rs319305 | snp | A/C/T | 0.609772 | 0.10292 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95973533 | ATCGGTCTAAAAAAA[A/C/T]ACTCACAACAAATAT | 1780 |
rs319306 | snp | A/T | 0.242201 | 0.249878 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95971338 | TTCTATTAAAGTTTT[A/T]AAAAATATATTGGAA | 1780 |
rs319307 | snp | A/G | 0.273587 | 0.248885 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95970912 | AGCCTTTATGATGCA[A/G]CTCCAGCAGCTTTAA | 1780 |
rs319308 | snp | A/G | 0.235564 | 0.249583 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95969833 | CTCATCGTACAGAGC[A/G]CTCCTGTTAACACTC | 1780 |
rs319309 | snp | C/T | 0.0391387 | 0.134304 | intron-variant, utr-variant-3-prime | DYNC1I1 | GRCh38.p7 | 7:96002172 | AAGCATGGTTGGGGT[C/T]GGGGAAAACTGAAGG | 1780 |
rs319310 | snp | C/T | 0.427119 | 0.176434 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95931450 | TTAAAAATGTAGTCA[C/T]AGGCCGGGCGCAGTG | 1780 |
rs319311 | snp | A/G | 0.231189 | 0.249291 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95931407 | aatcccagcactttg[A/G]gaggccgagtgggtg | 1780 |
rs319312 | snp | A/G | 0.272511 | 0.248984 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95929979 | CTTTCCTTGGGAAAT[A/G]TTTCTTAAGAGCCAG | 1780 |
rs319313 | snp | C/G | 0.245631 | 0.249962 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95929257 | GTGACACTCAGCCAG[C/G]CTTTGAGGACTGAGT | 1780 |
rs319314 | snp | C/T | 0.40733 | 0.194287 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95927318 | CATTGTATGGACGGT[C/T]ACCTCCCCTACTAGA | 1780 |
rs319315 | snp | C/G | 0.443195 | 0.158668 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96007363 | GAATTCATTCCATTG[C/G]TAGGCAAGATTCAAC | 1780 |
rs319316 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96006947 | tacacaatgtgtaat[A/G]attgaatcacagtag | 1780 |
rs319317 | snp | A/T | 0.453331 | 0.145452 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96020955 | ccattctactttctg[A/T]ctctacaaatttgac | 1780 |
rs319318 | snp | G/T | 0.458315 | 0.13822 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96018775 | AGAAACTTATGATAT[G/T]TCCCTCTGCTAGAAT | 1780 |
rs319319 | snp | C/G | 0.499987 | 0.00259581 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96016812 | TTGAAAAAGTACTAA[C/G]TCCTTGCAAAGGGGG | 1780 |
rs319320 | snp | C/G | 0.360632 | 0.224189 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95988100 | CTTGAGCCACCTCAC[C/G]CAGCCGAGTGATCAG | 1780 |
rs319321 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95984436 | ATGCTATTATGCTAT[G/T]GTACTATTGTCAAGC | 1780 |
rs319322 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95980645 | TGCACTTTGATGTCA[C/T]GTGGGCAAAAATGTC | 1780 |
rs319323 | snp | A/G | 0.116838 | 0.211584 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95979659 | AAGACCTTTAATGAT[A/G]GTTCTCCAACAAGTT | 1780 |
rs319324 | snp | A/G | 0.405776 | 0.195535 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95924133 | GCAAAGAAACTTGGG[A/G]AGATGCTCTGTAAAT | 1780 |
rs319325 | snp | C/T | 0.414245 | 0.188477 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95922802 | TGAAATGACAAATAA[C/T]TAAATAGTTCTACCT | 1780 |
rs319326 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95920969 | ATGTGAAAGCGGCCA[C/T]CTACTACTAAGTTAC | 1780 |
rs319327 | snp | A/C | 0.413748 | 0.188909 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95920788 | AAATGGCACCTATGA[A/C]AATAATAAATGTGTA | 1780 |
rs319328 | snp | C/T | 0.420255 | 0.183066 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95920400 | cacattgcatttatt[C/T]atcatgtctccttag | 1780 |
rs319329 | snp | C/G | 0.390464 | 0.206809 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95918719 | TCTCTATAAATTTTC[C/G]CCTTAAGGCCTCAGC | 1780 |
rs319330 | snp | A/C/G | 0.0694184 | 0.174917 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95916728 | GTTTTGCCGCTTTGT[A/C/G]CTGTCTTGGATTCCG | 1780 |
rs319331 | snp | C/T | 0.342358 | 0.232314 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95915051 | TCATTTAAGATATAA[C/T]TGAGATCATTCATTT | 1780 |
rs319332 | snp | C/T | 0.424348 | 0.179172 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95914788 | CTAGTCTGAATTCTC[C/T]CGGCTGGGTGCCAGC | 1780 |
rs319333 | snp | C/T | 0.26271 | 0.249677 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95914312 | ACATTCCTGATTATT[C/T]ACTGTATCCTTTTGT | 1780 |
rs319334 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95913566 | CAAAGGCATGTCTTA[C/T]GTGGCAGCAGGCAAG | 1780 |
rs319335 | snp | A/G | 0.243633 | 0.249919 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95963840 | GTATCCCTTGTTTTT[A/G]CTTTCTGGTCAGTCT | 1780 |
rs319336 | snp | A/T | 0.483852 | 0.0883933 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95960677 | TTATCTGCAGCTGTG[A/T]GGCCAACCGAGTGAA | 1780 |
rs319337 | snp | A/G | 0.44651 | 0.154543 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95960265 | acaaaaattagccag[A/G]agtggtggtgtccgc | 1780 |
rs319338 | snp | C/T | 0.237014 | 0.249662 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95960163 | gctgaaatagcacca[C/T]tgcactctagcctag | 1780 |
rs319339 | snp | A/C | 0.237593 | 0.249692 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95960078 | ttctcatttcacaaa[A/C]aacataaaggccaaa | 1780 |
rs319340 | snp | C/T | 0.445592 | 0.155704 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95958953 | GTAGACCAGCCCACC[C/T]ATTTGTCATTTGTAT | 1780 |
rs319341 | snp | C/T | 0.249038 | 0.249998 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95956447 | GCACATGTATACCTA[C/T]GTAACAAACTTGCAC | 1780 |
rs319342 | snp | C/T | 0.249038 | 0.249998 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95955471 | TTAAAAATTAAAAAT[C/T]AGCTAAGTGTGTAGT | 1780 |
rs319343 | snp | C/T | 0.249038 | 0.249998 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95955140 | ttatcaAAACCAGCA[C/T]GAATGCCTGGAAGTC | 1780 |
rs319344 | snp | A/T | 0.234692 | 0.249531 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95952697 | TTATATCTCCATTTA[A/T]ACAAAAAGGTTTTTG | 1780 |
rs319345 | snp | C/T | 0.441977 | 0.16014 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95948513 | CCAACTAGTAAACCA[C/T]TGAGGTTAACAAAGC | 1780 |
rs319346 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95947051 | TAAAATTTCTACCTG[C/T]ACCAGGGCTTTTGCA | 1780 |
rs319347 | snp | A/G | 0.283421 | 0.247756 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95945779 | TTTCTTTAAACAGCC[A/G]CTCTACTAATTCTTC | 1780 |
rs319348 | snp | C/T | 0.436123 | 0.166908 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95945648 | ATACCTGATGTTTAA[C/T]GCTAAAAAAGTGAAT | 1780 |
rs624967 | snp | A/G | | | intron-variant | DYNC1I1 | GRCh38.p7 | 7:95943933 | gaatgttaatgccta[A/G]gttttcttctagggt | 1780 |
rs720780 | snp | C/T | 0.443195 | 0.158668 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96007785 | GCCTGTTTCCCAAGG[C/T]GTCATCTTTCTTACT | 1780 |
rs735340 | snp | A/G | | | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96077286 | GAAGAATATTTCCCT[A/G]CCCCCTCCcacacac | 1780 |
rs735341 | snp | C/T | 0.205723 | 0.246048 | intron-variant | DYNC1I1 | GRCh38.p7 | 7:96077631 | GTTGCTTTAAATGAA[C/T]GAATTTCTCCTAGCA | 1780 |