SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1016418 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | DAW1 | GRCh38.p7 | 2:227880046 | ATCTTTACAGCATTG[A/G]GTTTTCTCATCCAGA | 164781 |
rs1112484 | snp | G/T | 0.275197 | 0.248727 | intron-variant | DAW1 | GRCh38.p7 | 2:227919785 | GGAACCAAGGGATTG[G/T]GCTGAGCTGGGAGGT | 164781 |
rs1524025 | snp | C/T | 0.270892 | 0.249126 | intron-variant, upstream-variant-2KB | DAW1 | GRCh38.p7 | 2:227888736 | AAAAAAGAGCCATTT[C/T]ACAAATCATGTCACA | 164781 |
rs1524026 | snp | A/G | 0.265727 | 0.249505 | intron-variant | DAW1 | GRCh38.p7 | 2:227877929 | AATTGAAACATGTAC[A/G]TTTGACTGCTTCGCT | 164781 |
rs1533960 | snp | G/T | 0.335312 | 0.234993 | intron-variant | DAW1 | GRCh38.p7 | 2:227918763 | TTTTTGAGAGGGGTG[G/T]GGATATATATAAATT | 164781 |
rs1533963 | snp | C/T | 0.225597 | 0.248806 | intron-variant | DAW1 | GRCh38.p7 | 2:227880293 | GCTGTATGCCACATG[C/T]TATAAAAAAGATTTA | 164781 |
rs1619037 | snp | C/T | 0.482609 | 0.0916147 | intron-variant | DAW1 | GRCh38.p7 | 2:227922723 | TGTGATTTCGGAAAC[C/T]GTCCATCATTAAGTA | 164781 |
rs1623450 | snp | C/G | 0.484491 | 0.0866827 | intron-variant | DAW1 | GRCh38.p7 | 2:227917188 | ATAGATGGATAGATA[C/G]ATAGATAGACAGACA | 164781 |
rs1624429 | snp | A/T | 0.456214 | 0.141336 | intron-variant | DAW1 | GRCh38.p7 | 2:227917047 | ATGTTGTCAGAGAGA[A/T]AACATAAACATAGTG | 164781 |
rs1625487 | snp | A/G | 0.265727 | 0.249505 | intron-variant | DAW1 | GRCh38.p7 | 2:227886344 | caagtgtgagcaacc[A/G]cgcccagctATTTGC | 164781 |
rs1627519 | snp | C/G | 0.257454 | 0.249889 | downstream-variant-500B | DAW1 | GRCh38.p7 | 2:227924736 | AACCTCCACCTCCTG[C/G]GTTCATGCGATTCTC | 164781 |
rs1628030 | snp | G/T | 0.247053 | 0.249983 | intron-variant | DAW1 | GRCh38.p7 | 2:227886069 | gagaatcgcttgaac[G/T]caggaggcggaggat | 164781 |
rs1715820 | snp | A/T | 0.269267 | 0.249256 | intron-variant | DAW1 | GRCh38.p7 | 2:227916574 | TGATGCAAAATAGTA[A/T]AGCACTCTACAAGGT | 164781 |
rs1715821 | snp | C/T | 0.483272 | 0.0899109 | intron-variant | DAW1 | GRCh38.p7 | 2:227915694 | AACATAGTACATATA[C/T]TCAGTGTTATTAAGA | 164781 |
rs1715828 | snp | A/T | 0.299366 | 0.245078 | missense, nc-transcript-variant, utr-variant-5-prime | DAW1 | GRCh38.p7 | 2:227893838 | CCTCTCCAGACGCAG[A/T]GTCCCAGAGCTTGCA | 164781 |
rs1715829 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | DAW1 | GRCh38.p7 | 2:227910350 | GAGTAGTTAGGTCTA[C/T]AGGTGCATGCCACCA | 164781 |
rs1715830 | snp | C/T | 0.482979 | 0.0906686 | intron-variant | DAW1 | GRCh38.p7 | 2:227910334 | AGGTGCATGCCACCA[C/T]ACCTGACTAATTTTT | 164781 |
rs1715833 | snp | C/T | 0 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227906531 | AAGCAATTCAAATTG[C/T]TTTACTACATCACAA | 164781 |
rs1715834 | snp | A/C | 0.462582 | 0.131564 | intron-variant | DAW1 | GRCh38.p7 | 2:227903441 | ACAGTCATTGCTCTA[A/C]GGATTCTCTTGTCAT | 164781 |
rs1715835 | snp | C/T | 0.251296 | 0.249997 | intron-variant | DAW1 | GRCh38.p7 | 2:227923574 | CAGCAACTTTGAATA[C/T]CTCCAGGTTTGGATG | 164781 |
rs1715836 | snp | C/T | 0.482757 | 0.0912364 | intron-variant | DAW1 | GRCh38.p7 | 2:227923050 | CAACGCAAGGCACAA[C/T]AACAAAAATTCTTTT | 164781 |
rs1715837 | snp | A/T | 0.482459 | 0.0919928 | intron-variant | DAW1 | GRCh38.p7 | 2:227922875 | AGCCCCTCACCTCTT[A/T]TCTCATCAAGGAGAA | 164781 |
rs1715838 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | DAW1 | GRCh38.p7 | 2:227921069 | TTCTCTGTGCAAAGA[C/T]GCAGGGCCCTGGTGT | 164781 |
rs1715839 | snp | A/C | 0.238749 | 0.249747 | intron-variant | DAW1 | GRCh38.p7 | 2:227886093 | gattctcTGTGCCCA[A/C]CCAGTGACCTTTACA | 164781 |
rs1715840 | snp | A/T | 0.239326 | 0.249772 | intron-variant | DAW1 | GRCh38.p7 | 2:227890764 | agggaacatttttga[A/T]ggtgaaagtagatgc | 164781 |
rs1715841 | snp | A/G | 0.239902 | 0.249796 | intron-variant | DAW1 | GRCh38.p7 | 2:227891693 | AAGTCTCTGTTGAGA[A/G]CATGGCTGTGATCAG | 164781 |
rs1715846 | snp | C/T | 0.264906 | 0.249555 | intron-variant | DAW1 | GRCh38.p7 | 2:227881967 | gtcaggagtttgaga[C/T]cagcctggccaacat | 164781 |
rs1715849 | snp | C/T | 0.5 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227917138 | AGACAGACAGATAGA[C/T]AGATAGATAGATAGA | 164781 |
rs1715850 | snp | C/T | 0.375 | 0.216506 | intron-variant | DAW1 | GRCh38.p7 | 2:227917134 | AGACAGATAGATAGA[C/T]AGATAGATAGATAGA | 164781 |
rs1715851 | snp | C/T | 0.490007 | 0.0699769 | intron-variant | DAW1 | GRCh38.p7 | 2:227917130 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 164781 |
rs1721333 | snp | C/T | 0.361684 | 0.223667 | intron-variant | DAW1 | GRCh38.p7 | 2:227909270 | agacagacagacaga[C/T]agatagatagataga | 164781 |
rs1721334 | snp | A/T | 0.26078 | 0.249767 | intron-variant | DAW1 | GRCh38.p7 | 2:227906707 | AATTCCATAGTATAA[A/T]CTCTTAGTAACCATT | 164781 |
rs1721337 | snp | A/C | 0.277334 | 0.248501 | intron-variant | DAW1 | GRCh38.p7 | 2:227905882 | ctgtagtccctgcta[A/C]tcgggaggctgaagc | 164781 |
rs1721338 | snp | A/G | 0.464841 | 0.127841 | intron-variant | DAW1 | GRCh38.p7 | 2:227905823 | AGCTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 164781 |
rs1721339 | snp | C/G | 0.465368 | 0.126951 | intron-variant | DAW1 | GRCh38.p7 | 2:227905583 | ACACATCAAGTAACT[C/G]AAAGGTCCTTCTTCC | 164781 |
rs1721340 | snp | C/T | 0.464309 | 0.12873 | intron-variant | DAW1 | GRCh38.p7 | 2:227903808 | GTTTTTAAAAATGTA[C/T]TTATAATTTTGAAAG | 164781 |
rs1721341 | snp | C/T | 0.464309 | 0.12873 | intron-variant | DAW1 | GRCh38.p7 | 2:227903768 | ACTGAATTTCCCATC[C/T]GGCTGTTCCTGCTGA | 164781 |
rs1721343 | snp | A/C | 0.258288 | 0.249863 | downstream-variant-500B | DAW1 | GRCh38.p7 | 2:227924680 | GACTACAGGCCCCCA[A/C]CACCACGCCCGCCTG | 164781 |
rs1721344 | snp | A/G | 0.482683 | 0.0914256 | intron-variant | DAW1 | GRCh38.p7 | 2:227923768 | AGCTCAGGCATTTTT[A/G]AAGTAGTGATTTTTT | 164781 |
rs1721345 | snp | A/G | 0.25634 | 0.24992 | intron-variant | DAW1 | GRCh38.p7 | 2:227923665 | TGGCTTCTCAGAATG[A/G]GAGAGAACTTGAGAA | 164781 |
rs1721346 | snp | C/G | 0.482757 | 0.0912364 | intron-variant | DAW1 | GRCh38.p7 | 2:227923289 | TCCAGCCTCAGGTAG[C/G]CCACTACAAAATGCC | 164781 |
rs1721347 | snp | C/G | 0.256619 | 0.249912 | intron-variant | DAW1 | GRCh38.p7 | 2:227922945 | ATGTGGACTAGGAAA[C/G]GCTGGTCTTCCTTCT | 164781 |
rs1721348 | snp | C/T | 0.233235 | 0.249437 | intron-variant | DAW1 | GRCh38.p7 | 2:227922730 | TAAGCCCTGTGATTT[C/T]GGAAACTGTCCATCA | 164781 |
rs1721349 | snp | C/G | 0.483563 | 0.0891524 | intron-variant | DAW1 | GRCh38.p7 | 2:227921954 | ATGTTGCCCAGGCTG[C/G]CCTCAAGCATTTTTT | 164781 |
rs1721350 | snp | A/G | 0.483418 | 0.0895317 | intron-variant | DAW1 | GRCh38.p7 | 2:227920775 | GCAGGAGAATCGCTT[A/G]AACCTGGGAGGTGGA | 164781 |
rs1721354 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | DAW1 | GRCh38.p7 | 2:227918420 | AAGACCAGCATGATA[A/C]ACTAGGTGTGAGTCT | 164781 |
rs1721355 | snp | A/G | 0.483418 | 0.0895317 | intron-variant | DAW1 | GRCh38.p7 | 2:227918260 | TCCAGCGCCAAAAGC[A/G]CCAAGCATATATTAG | 164781 |
rs1721356 | snp | C/T | 0.238749 | 0.249747 | intron-variant | DAW1 | GRCh38.p7 | 2:227890151 | TTTAACAAATAATTA[C/T]TGGGACAATCTTAGC | 164781 |
rs1721357 | snp | C/T | 0.247053 | 0.249983 | intron-variant, upstream-variant-2KB | DAW1 | GRCh38.p7 | 2:227889256 | GAGAAACAAATAACC[C/T]TGTTTCAGGTCTTTC | 164781 |
rs1721358 | snp | A/G | 0.235273 | 0.249566 | intron-variant, upstream-variant-2KB | DAW1 | GRCh38.p7 | 2:227887415 | AGATTAGATTCTTAC[A/G]TATGTGTTGAAGGTA | 164781 |
rs1721359 | snp | C/T | 0.422315 | 0.181128 | intron-variant | DAW1 | GRCh38.p7 | 2:227887158 | TTTGTGCCAAGCACC[C/T]GAAATAAGACTTGGA | 164781 |
rs1721374 | snp | A/G | 0.275464 | 0.2487 | intron-variant | DAW1 | GRCh38.p7 | 2:227899503 | CCTACTGACAGTTAC[A/G]GGAGAGGTGGTTATA | 164781 |
rs1721375 | snp | C/T | 0.269267 | 0.249256 | intron-variant | DAW1 | GRCh38.p7 | 2:227915355 | TAAGTTGATGACACA[C/T]AAGTGATGACACATA | 164781 |
rs1916803 | snp | A/C | 0.495445 | 0.0475058 | intron-variant, upstream-variant-2KB | DAW1 | GRCh38.p7 | 2:227888317 | CTGTCTCAGTATCCA[A/C]TTCCCATGAATGTGG | 164781 |
rs1969421 | snp | C/T | 0.47852 | 0.101384 | intron-variant | DAW1 | GRCh38.p7 | 2:227905880 | gtagtccctgctaat[C/T]gggaggctgaagcag | 164781 |
rs1969422 | snp | A/G | 0.478437 | 0.10157 | intron-variant | DAW1 | GRCh38.p7 | 2:227905869 | taatcgggaggctga[A/G]gcaggagaatggcgt | 164781 |
rs1969423 | snp | A/G | 0.280785 | 0.248097 | intron-variant | DAW1 | GRCh38.p7 | 2:227905847 | gaatggcgtgaaccc[A/G]ggaagcggagcttgc | 164781 |
rs1996959 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | DAW1 | GRCh38.p7 | 2:227909053 | AGTATAGTATCATAC[A/G]TTATTATAAAGAGGA | 164781 |
rs2056570 | snp | A/C | 0.200492 | 0.245049 | intron-variant | DAW1 | GRCh38.p7 | 2:227887099 | ATGCCCCAGCCCCAC[A/C]CTAGACACGTGCTCC | 164781 |
rs2177466 | snp | C/T | 0.495483 | 0.0473088 | intron-variant | DAW1 | GRCh38.p7 | 2:227886713 | GTGATCCTCCTGCCT[C/T]GATCTCCCAAGATGC | 164781 |
rs2396510 | snp | C/T | 0.495407 | 0.0477027 | intron-variant | DAW1 | GRCh38.p7 | 2:227886036 | CTGGAGTGCAGTGGC[C/T]CGATCTCGGCTCATT | 164781 |
rs2396511 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | DAW1 | GRCh38.p7 | 2:227917330 | CAGTGGCACTATCTC[A/G]GCTCACTGCAAGCTC | 164781 |
rs2396512 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | DAW1 | GRCh38.p7 | 2:227917346 | GCTCACTGCAAGCTC[C/T]ACCTCCTGGGTTCAT | 164781 |
rs2396513 | snp | A/G | 0.483563 | 0.0891524 | intron-variant | DAW1 | GRCh38.p7 | 2:227917347 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCATG | 164781 |
rs2396514 | snp | C/T | 0.483199 | 0.0901004 | intron-variant | DAW1 | GRCh38.p7 | 2:227917487 | GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCC | 164781 |
rs2396515 | snp | G/T | 0 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227917503 | CTGACCTCGTGATCC[G/T]CCCGCCTCGGCCTCC | 164781 |
rs2946930 | snp | A/T | 0.483995 | 0.0880135 | intron-variant | DAW1 | GRCh38.p7 | 2:227909533 | CAGATGGCATATGGC[A/T]AGACTTCTCAGCCTT | 164781 |
rs2946931 | snp | A/C | 0.460813 | 0.134379 | intron-variant | DAW1 | GRCh38.p7 | 2:227902915 | TCCAGATGCAATTAC[A/C]TTACCAGATTCCATC | 164781 |
rs2949014 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | DAW1 | GRCh38.p7 | 2:227902902 | GTACAAAGAATTAGA[C/T]GGAATCTGGTAAGGT | 164781 |
rs2949015 | snp | A/C | 0.482905 | 0.0908579 | intron-variant | DAW1 | GRCh38.p7 | 2:227910427 | CAGCGAACTATGATT[A/C]TGCCACTATAATCCA | 164781 |
rs2949016 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | DAW1 | GRCh38.p7 | 2:227910465 | TGACAGAGTGAGACC[C/T]CATCTTCTTGATGAA | 164781 |
rs2949017 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | DAW1 | GRCh38.p7 | 2:227917158 | tctgtctgtctgtct[A/G]tctgtctgtctgtct | 164781 |
rs3057652 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227885991 | ttttttttttttttt[-/T/TT/TTT]gagacagagtttcac | 164781 |
rs3057690 | in-del | -/ATCT/ATCTATCT/ATCTATCTATCT/ATCTGTCT | 0 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227909273 | TCTATCTATCTATCT[lengthTooLong]GTCTGTCTGTCTGTC | 164781 |
rs3748862 | snp | A/G | 0.499952 | 0.004891 | intron-variant, nc-transcript-variant | DAW1 | GRCh38.p7 | 2:227912280 | GTGCCACTGCACTCC[A/G]GCCTGGGCGACAGAG | 164781 |
rs3748863 | snp | C/T | 0.493883 | 0.0549634 | intron-variant | DAW1 | GRCh38.p7 | 2:227912222 | AAAAGAGAAAGAAGG[C/T]GACATAGATATAGCA | 164781 |
rs4145724 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | DAW1 | GRCh38.p7 | 2:227872531 | CGATGAGGTATCGCA[C/T]AGAGATCTCATGATT | 164781 |
rs4319923 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | DAW1 | GRCh38.p7 | 2:227917434 | CCCGGCTAATTTGTT[A/G]TATTTTTAGTAGAGA | 164781 |
rs4972991 | snp | A/G | 0 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227872293 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAAA | 164781 |
rs4972994 | snp | A/G | 0.498964 | 0.02274 | intron-variant | DAW1 | GRCh38.p7 | 2:227876211 | atttttagtagagac[A/G]gggtttcaccgtgtt | 164781 |
rs4972998 | snp | G/T | 0.49998 | 0.00319482 | intron-variant | DAW1 | GRCh38.p7 | 2:227878632 | GAAAATGAGGCAGAA[G/T]AATGGCATGGGTTCC | 164781 |
rs4972999 | snp | G/T | 0.499974 | 0.00359416 | intron-variant | DAW1 | GRCh38.p7 | 2:227878679 | CAGTGAGTGATGATT[G/T]TACAACTGCACTGCA | 164781 |
rs4973000 | snp | C/T | 0.49998 | 0.00319482 | intron-variant | DAW1 | GRCh38.p7 | 2:227878945 | ggcatgccaccacac[C/T]tggctaattttttct | 164781 |
rs4973006 | snp | G/T | 0.499977 | 0.00339449 | intron-variant | DAW1 | GRCh38.p7 | 2:227882160 | CTAGAATTATATCTG[G/T]TATATCAAACTATGG | 164781 |
rs4973021 | snp | A/C | 0.478437 | 0.10157 | intron-variant | DAW1 | GRCh38.p7 | 2:227916475 | ATTCTCTTTGATAGT[A/C]ACGTATTATGAATGT | 164781 |
rs4973398 | snp | A/G | 0.48 | 0.0979796 | intron-variant | DAW1 | GRCh38.p7 | 2:227872297 | AAAAAAAAAAAGAAA[A/G]AAAAGAAAAAAATCT | 164781 |
rs4973424 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | DAW1 | GRCh38.p7 | 2:227879051 | tcggcctcccaaagt[A/G]ctggaattacaggca | 164781 |
rs4973445 | snp | G/T | 0.495368 | 0.0478996 | intron-variant | DAW1 | GRCh38.p7 | 2:227885523 | CAGATAATACATTAT[G/T]TTTTAAAAATTGTTC | 164781 |
rs4973478 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | DAW1 | GRCh38.p7 | 2:227901016 | TGTTGAGACTTTTTG[A/G]CTAGGAGATGGTATG | 164781 |
rs4973494 | snp | A/C | 0.235273 | 0.249566 | intron-variant | DAW1 | GRCh38.p7 | 2:227918648 | AGTATCTGGCTCTCA[A/C]CACAGGCAAGAAGAT | 164781 |
rs5021749 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | DAW1 | GRCh38.p7 | 2:227876030 | TCTCTCTTTTTTTTT[G/T]TTTGAGATGGAGTCT | 164781 |
rs5839244 | in-del | -/T | | | intron-variant | DAW1 | GRCh38.p7 | 2:227919547 | AGTATCAAGTGTTCT[-/T]GTAAGTTAGATGCAA | 164781 |
rs6707569 | snp | A/G | 0.495407 | 0.0477027 | intron-variant, upstream-variant-2KB | DAW1 | GRCh38.p7 | 2:227889319 | CCCTACAAGTTTGGC[A/G]TCTGATGAGGGCTGC | 164781 |
rs6710425 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DAW1 | GRCh38.p7 | 2:227874742 | taaaaactatcCTGa[A/C]ctgaggtcaggagtt | 164781 |
rs6713891 | snp | G/T | 0.0748431 | 0.178382 | intron-variant | DAW1 | GRCh38.p7 | 2:227908608 | GCAAGTATTTATGAT[G/T]CTACTCTATGTCTGC | 164781 |
rs6715951 | snp | A/T | 0.000546923 | 0.0165276 | missense, nc-transcript-variant | DAW1 | GRCh38.p7 | 2:227921399 | CTTTCTCTTTTGCAG[A/T]TTTCTTTCAACCCTC | 164781 |
rs6720047 | snp | A/G | 0 | 0 | intron-variant | DAW1 | GRCh38.p7 | 2:227922428 | TGACAAGATGATGGT[A/G]TCATGTTAGTGGAGT | 164781 |
rs6720168 | snp | A/G | | | intron-variant | DAW1 | GRCh38.p7 | 2:227922536 | CAGATCTGCCTAAGT[A/G]CCAGTGATTCTCATC | 164781 |
rs6722145 | snp | A/C | 0.300926 | 0.244758 | upstream-variant-2KB | DAW1 | GRCh38.p7 | 2:227870014 | ACATTATAGCAGCAG[A/C]CTTTACTGGTCATGA | 164781 |
rs6723413 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | DAW1 | GRCh38.p7 | 2:227905759 | GAAATTATTTATTTA[G/T]TTAGTTAGtttttga | 164781 |