SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs20411 | snp | A/C | 0.485255 | 0.0845871 | intron-variant | NBEA | GRCh38.p7 | 13:35657351 | TCTTTTCCCTCAAAT[A/C]AAGATCACATCTTGT | 26960 |
rs374452 | snp | A/G | 0.41023 | 0.191902 | utr-variant-3-prime | NBEA | GRCh38.p7 | 13:35672299 | AAATGACTGCGAGTG[A/G]GTGTAAATTCTGAGA | 26960 |
rs378833 | snp | C/T | 0.123452 | 0.215605 | intron-variant | NBEA | GRCh38.p7 | 13:35658174 | AAAACTAAAATATGA[C/T]ACTGCTTTTTAACAA | 26960 |
rs399518 | snp | C/T | 0.103082 | 0.202275 | intron-variant | NBEA | GRCh38.p7 | 13:35610130 | CAGCTAAGAAGACAG[C/T]GTGAGCTATGAGCAG | 26960 |
rs403904 | snp | C/T | 0.405082 | 0.196086 | utr-variant-3-prime | NBEA | GRCh38.p7 | 13:35672096 | TCATAAAAGATGAAA[C/T]GCCTTAGGCTAAGAA | 26960 |
rs410595 | snp | A/C | 0.101301 | 0.200969 | intron-variant | NBEA | GRCh38.p7 | 13:35627202 | TTAGAAAATTGTCTT[A/C]CATGGCTCTGCAATA | 26960 |
rs413464 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | NBEA | GRCh38.p7 | 13:35648888 | ggtgggaggggagca[G/T]caggaagaacagcta | 26960 |
rs433928 | snp | A/C | 0.151001 | 0.229563 | intron-variant | NBEA | GRCh38.p7 | 13:35621174 | TGAATATAGTCTAAT[A/C]TCTCTCCTGCCCCAG | 26960 |
rs435729 | snp | A/G | 0.151001 | 0.229563 | intron-variant | NBEA | GRCh38.p7 | 13:35626960 | AAAATTTTGAAAGGA[A/G]TAAATCAGGAAAGGG | 26960 |
rs442429 | snp | A/T | | | intron-variant | NBEA | GRCh38.p7 | 13:35658274 | GCTTTTCACTAAAAA[A/T]AAATTCCTATAGATG | 26960 |
rs475515 | snp | C/T | | | intron-variant | NBEA | GRCh38.p7 | 13:35163525 | gtagtcccagctact[C/T]gggaatctcctgggc | 26960 |
rs480282 | snp | C/T | 0.33693 | 0.2344 | intron-variant | NBEA | GRCh38.p7 | 13:35333818 | ttatgttaaatgaaa[C/T]aggacaggcacagaa | 26960 |
rs480359 | snp | A/G | 0.306679 | 0.24349 | intron-variant | NBEA | GRCh38.p7 | 13:35333787 | aaagacaaacagcat[A/G]ttctcactcatttgt | 26960 |
rs483335 | snp | A/G | 0.43555 | 0.167544 | intron-variant | NBEA | GRCh38.p7 | 13:35363384 | GGCATGGCTATATGG[A/G]TTCCTGCCATTTCAT | 26960 |
rs483801 | snp | G/T | 0.187685 | 0.242109 | intron-variant | NBEA | GRCh38.p7 | 13:35157865 | ATAGAAGAAGCATGG[G/T]TGTCAGAAGTATGGC | 26960 |
rs486056 | snp | C/G | 0.405429 | 0.195811 | intron-variant | NBEA | GRCh38.p7 | 13:35363665 | ATTTTGCTTATTTCT[C/G]TGATCCATTTGGATT | 26960 |
rs487005 | snp | A/G | 0.43555 | 0.167544 | intron-variant | NBEA | GRCh38.p7 | 13:35363773 | TCTTCTCCCTTGGAT[A/G]TTTGAACCTCTGACA | 26960 |
rs487134 | snp | A/G | 0.43555 | 0.167544 | intron-variant | NBEA | GRCh38.p7 | 13:35363812 | ATCATGTTCTAGCTA[A/G]ATGATTAATTCTAAC | 26960 |
rs493112 | snp | C/T | 0.408871 | 0.193029 | intron-variant | NBEA | GRCh38.p7 | 13:35356276 | TCTAAAACAGGTGTT[C/T]ACAAATCCAGTAACA | 26960 |
rs499570 | snp | A/G | 0.241914 | 0.249869 | intron-variant | NBEA | GRCh38.p7 | 13:35324071 | AGGAGCCTAGAGTTG[A/G]CCTTTGCATTTGTGG | 26960 |
rs503992 | snp | C/T | 0.43555 | 0.167544 | intron-variant | NBEA | GRCh38.p7 | 13:35360478 | acaatccaaaactac[C/T]caatatacaaaggaa | 26960 |
rs509182 | snp | C/G | 0.435694 | 0.167385 | intron-variant | NBEA | GRCh38.p7 | 13:35363883 | AATCATTGTGACTTA[C/G]TGATTGAATAAATAG | 26960 |
rs511816 | snp | C/G | 0.435837 | 0.167226 | intron-variant | NBEA | GRCh38.p7 | 13:35364152 | TTCTCTTATGGCCAA[C/G]AAATTTCATCTCTCC | 26960 |
rs512749 | snp | A/G | 0.43555 | 0.167544 | intron-variant | NBEA | GRCh38.p7 | 13:35364277 | CTATCAGCAAGTCCA[A/G]CAACACATGTAGAGT | 26960 |
rs516842 | snp | A/G | 0.286825 | 0.247273 | intron-variant | NBEA | GRCh38.p7 | 13:35125762 | GCACTTAGCAGAAAA[A/G]TATTGCTATGGAATA | 26960 |
rs520798 | snp | A/G | 0.363985 | 0.222503 | intron-variant | NBEA | GRCh38.p7 | 13:35300379 | GAAATGTGCATCAGT[A/G]TAAAAGAATATAATC | 26960 |
rs523046 | snp | A/G | 0.18989 | 0.242666 | intron-variant | NBEA | GRCh38.p7 | 13:35129295 | aaacttagaaatgtt[A/G]gataaaaatatgtca | 26960 |
rs543106 | snp | A/G | 0.377385 | 0.215112 | intron-variant | NBEA | GRCh38.p7 | 13:35344868 | CTCCTAGAGATCAGA[A/G]ACAGGGAATGTTCCA | 26960 |
rs550665 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NBEA | GRCh38.p7 | 13:35628743 | gccaatatgctgaaa[C/T]cccatctctacaaaa | 26960 |
rs554163 | snp | A/T | 0.47666 | 0.105476 | intron-variant | NBEA | GRCh38.p7 | 13:35628620 | ATTCTTAAAAATAAC[A/T]GCACAAGTGCTAGGA | 26960 |
rs562861 | snp | C/T | 0.111928 | 0.208413 | intron-variant | NBEA | GRCh38.p7 | 13:35106321 | ATGTATTTCCTTTGA[C/T]TAACGGTTTTAAAAT | 26960 |
rs568303 | snp | G/T | 0.189576 | 0.242588 | intron-variant | NBEA | GRCh38.p7 | 13:35166740 | TTGTTTTTGTATTAC[G/T]GGGTTGTATAATATT | 26960 |
rs572549 | snp | A/G | 0.445855 | 0.155373 | intron-variant | NBEA | GRCh38.p7 | 13:35372797 | gcagcagccaacagc[A/G]tggcagctgtgggtg | 26960 |
rs581802 | snp | C/T | 0 | 0 | intron-variant | NBEA | GRCh38.p7 | 13:35331735 | CTGTTAACTGACTTC[C/T]TTTTTCTGGTATTCA | 26960 |
rs589524 | snp | C/T | 0.362732 | 0.22314 | intron-variant | NBEA | GRCh38.p7 | 13:35157827 | GGAAATTCAGAGTTA[C/T]GGGTTTCTCATCATG | 26960 |
rs591936 | snp | C/T | 0.318415 | 0.240457 | intron-variant | NBEA | GRCh38.p7 | 13:35339646 | taatgctgacatctt[C/T]ttggcttctgggagg | 26960 |
rs592906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NBEA | GRCh38.p7 | 13:35140667 | GTATCAACAATCCTG[C/T]GTCTTTTGTTATGGA | 26960 |
rs593693 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NBEA | GRCh38.p7 | 13:35162994 | CTAGAGATGGTAACT[A/G]AGGAAACCTAAATAC | 26960 |
rs601848 | snp | A/C | 0.435837 | 0.167226 | intron-variant | NBEA | GRCh38.p7 | 13:35372582 | gatagcaacaactgc[A/C]ctgtggcctttctgc | 26960 |
rs610757 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NBEA | GRCh38.p7 | 13:35139006 | ACAGTAAAGAAAACA[A/G/T]TAAAGAAAGAAAAGA | 26960 |
rs611498 | snp | C/G | 0.142609 | 0.225759 | intron-variant | NBEA | GRCh38.p7 | 13:35079808 | AACGTTTTGGAATAG[C/G]TTAGTAGTGAGTGAC | 26960 |
rs615554 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | NBEA | GRCh38.p7 | 13:35118873 | TTTAGTGGTTTTTTT[C/T]TTTCAGCTGGTGATG | 26960 |
rs619619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NBEA | GRCh38.p7 | 13:35124745 | tccatacatatgtgt[A/G]tatatatccatacat | 26960 |
rs625622 | snp | C/T | 0.145978 | 0.227331 | intron-variant | NBEA | GRCh38.p7 | 13:35138018 | TACTAATTATGAGAT[C/T]CCTAATAATATCAGG | 26960 |
rs631616 | snp | C/T | 0.445724 | 0.155538 | intron-variant | NBEA | GRCh38.p7 | 13:35371938 | ccaacaaaactttac[C/T]acagcctccacaaac | 26960 |
rs633471 | snp | A/C | 0.030665 | 0.119967 | intron-variant | NBEA | GRCh38.p7 | 13:35371469 | aagaggtatcataac[A/C]aacaaacaaacagga | 26960 |
rs651810 | snp | A/C | 0.43555 | 0.167544 | intron-variant | NBEA | GRCh38.p7 | 13:35376287 | TTGAATGTTTCAAGT[A/C]ATTCTGGAGTGAAAG | 26960 |
rs653114 | snp | A/G | 0.320814 | 0.239761 | intron-variant | NBEA | GRCh38.p7 | 13:35336075 | tttaaggaaatctct[A/G]ttcaattattagctg | 26960 |
rs657831 | snp | C/T | 0.420415 | 0.182917 | intron-variant | NBEA | GRCh38.p7 | 13:35356008 | ataatgtaatagatt[C/T]tttgctcttttatcc | 26960 |
rs661387 | snp | C/G | | | intron-variant | NBEA | GRCh38.p7 | 13:35154711 | AGGAAAGAGAAAATT[C/G]TAAAACAtttactaa | 26960 |
rs666915 | snp | A/C | 0.31014 | 0.242659 | intron-variant | NBEA | GRCh38.p7 | 13:35343469 | AAGCAAACATGTAAC[A/C]TGTGTAAAATCTGAT | 26960 |
rs669933 | snp | A/C | 0.434543 | 0.168653 | intron-variant | NBEA | GRCh38.p7 | 13:35363318 | TAGGTCTGTTTCTGG[A/C]CAAAATGCTACATTA | 26960 |
rs673003 | snp | A/C | 0.434976 | 0.168179 | intron-variant | NBEA | GRCh38.p7 | 13:35363964 | CACTCTTGGAACTGA[A/C]AAATGCAGAAGGAAC | 26960 |
rs673481 | snp | A/G | 0.445724 | 0.155538 | intron-variant | NBEA | GRCh38.p7 | 13:35364119 | GTGATAACCTTCTCA[A/G]ACATATCCAAAACAT | 26960 |
rs673501 | snp | C/T | 0.43598 | 0.167067 | intron-variant | NBEA | GRCh38.p7 | 13:35364136 | CATATCCAAAACATA[C/T]TTCTCTTATGGCCAA | 26960 |
rs675673 | snp | C/G | 0.410061 | 0.192043 | intron-variant | NBEA | GRCh38.p7 | 13:35357689 | catattttctttata[C/G]agtctatcatttatg | 26960 |
rs685311 | snp | C/T | 0.445592 | 0.155704 | intron-variant | NBEA | GRCh38.p7 | 13:35364402 | AGGTAAATATTGAGA[C/T]ACAAGTAAGGAAGTG | 26960 |
rs693032 | snp | A/T | 0.325563 | 0.238307 | intron-variant | NBEA | GRCh38.p7 | 13:35334006 | agttatctacactct[A/T]acgtctgttgcagta | 26960 |
rs720506 | snp | A/G | 0.20511 | 0.245937 | intron-variant | NBEA | GRCh38.p7 | 13:35045597 | tgggtagaggggaat[A/G]tcttccaacaggcac | 26960 |
rs728991 | snp | C/G | 0.123105 | 0.215401 | intron-variant | NBEA | GRCh38.p7 | 13:35616784 | TGGTCATATTAGTAT[C/G]AGGAGTAAATTATTT | 26960 |
rs728992 | snp | A/T | 0.333722 | 0.235565 | intron-variant | NBEA | GRCh38.p7 | 13:35616658 | TTACAGTAAGAGGGA[A/T]AACCTACTTCAGAGT | 26960 |
rs728993 | snp | C/T | 0.323434 | 0.238972 | intron-variant | NBEA | GRCh38.p7 | 13:35616476 | ACATGTGTACTGAGA[C/T]AGACCAGAGTGTCAC | 26960 |
rs728994 | snp | A/C | 0.323197 | 0.239044 | intron-variant | NBEA | GRCh38.p7 | 13:35616919 | ACAGGGATGCTACAC[A/C]GTGAGGCTTATTTTA | 26960 |
rs766768 | snp | A/G | 0.100588 | 0.200439 | intron-variant | NBEA | GRCh38.p7 | 13:35654313 | AGGCCTGGATTGTCA[A/G]CAGACAGAAGGCCTT | 26960 |
rs795389 | snp | A/G | 0.144296 | 0.226554 | intron-variant | NBEA | GRCh38.p7 | 13:35154866 | tgtggtggctcatgc[A/G]tttaatcccagcact | 26960 |
rs797043 | snp | A/G | | | intron-variant | NBEA | GRCh38.p7 | 13:35612218 | gtgaacccaggaggc[A/G]gagcttgcagtgagc | 26960 |
rs797053 | snp | C/T | 0 | 0 | intron-variant | NBEA | GRCh38.p7 | 13:35162390 | AGTAGCAAGGGCAAC[C/T]TAAATGATCTAGCAC | 26960 |
rs811218 | snp | A/G | | | intron-variant | NBEA | GRCh38.p7 | 13:35612257 | tagtcccagctactc[A/G]ggaggctgaggcagg | 26960 |
rs812163 | snp | A/G | | | intron-variant | NBEA | GRCh38.p7 | 13:35612140 | gtctcaaaaaaaaaa[A/G]aaaaaaaaatattgt | 26960 |
rs813252 | snp | C/T | | | intron-variant | NBEA | GRCh38.p7 | 13:35612210 | aggaggcggagcttg[C/T]agtgagccgagatcg | 26960 |
rs867503 | snp | C/G | 0.157642 | 0.232314 | intron-variant | NBEA | GRCh38.p7 | 13:35222110 | TTTAACATTTACACT[C/G]CATCTAATATATGAT | 26960 |
rs867963 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | NBEA | GRCh38.p7 | 13:35604140 | AACTCATGATAGTCA[C/T]TGCTGATAGAATAGT | 26960 |
rs870479 | snp | A/T | 0.382473 | 0.212016 | intron-variant | NBEA | GRCh38.p7 | 13:35604770 | AATGGTGAGAAACTG[A/T]GCACAAGAGGAGAAC | 26960 |
rs913403 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NBEA | GRCh38.p7 | 13:35604760 | AATATACCCTGTTCT[C/T]CTCTTGTGCTCAGTT | 26960 |
rs936496 | snp | C/T | 0.491783 | 0.0635686 | intron-variant | NBEA | GRCh38.p7 | 13:35526404 | cgggcctcgacctcc[C/T]aaagtgctgagatta | 26960 |
rs951751 | snp | A/G | | | intron-variant | NBEA | GRCh38.p7 | 13:35192806 | AAACAAAATACCTAA[A/G]GAAATAAAATCTGAT | 26960 |
rs951752 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | NBEA | GRCh38.p7 | 13:35192757 | CACATCAAAAGACTT[C/T]TGCCACCAACTACAT | 26960 |
rs951791 | snp | A/G | 0.300421 | 0.244863 | intron-variant | NBEA | GRCh38.p7 | 13:35230866 | gtctgtgtgtacggc[A/G]agcatttgttagaag | 26960 |
rs951792 | snp | G/T | 0.093777 | 0.195178 | intron-variant | NBEA | GRCh38.p7 | 13:35231027 | TTACTGAAATTAAGA[G/T]ATTTCAATAGTCTCC | 26960 |
rs953848 | snp | C/T | 0.100588 | 0.200439 | intron-variant | NBEA | GRCh38.p7 | 13:35624689 | TAGAAATGAAAAATA[C/T]AGAAAGCTGGACACA | 26960 |
rs958792 | snp | C/T | 0.47802 | 0.102502 | intron-variant | NBEA | GRCh38.p7 | 13:35502557 | CAATCTGCTTCCACA[C/T]GGTAAGCAGATAAAT | 26960 |
rs958793 | snp | A/G | 0.478188 | 0.10213 | intron-variant | NBEA | GRCh38.p7 | 13:35502418 | ATGTAACTTAAAACT[A/G]AGCCTAAAACTTTCC | 26960 |
rs959732 | snp | A/G | 0.177503 | 0.239258 | intron-variant | NBEA | GRCh38.p7 | 13:35493951 | ATTCATTTTTAAAAG[A/G]TTTATTGTAAGGATC | 26960 |
rs975284 | snp | A/C | 0.306927 | 0.243432 | intron-variant | NBEA | GRCh38.p7 | 13:35551440 | AACAATAAAACCCTG[A/C]GAGTTTATTAAGGGT | 26960 |
rs981386 | snp | A/G | 0.327211 | 0.237778 | intron-variant | NBEA | GRCh38.p7 | 13:35515400 | GCCACCTCCCTTTTT[A/G]TCAAAATACACATAA | 26960 |
rs981387 | snp | A/T | 0.327211 | 0.237778 | intron-variant | NBEA | GRCh38.p7 | 13:35515522 | TTTGATTATTAATTA[A/T]GCTTTTAAAACCCAA | 26960 |
rs995180 | snp | A/T | 0.284209 | 0.247648 | intron-variant | NBEA | GRCh38.p7 | 13:35658815 | AGCTTTTTAAATAGA[A/T]AAGTGGGTCACAAAT | 26960 |
rs999336 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NBEA | GRCh38.p7 | 13:34966056 | TGTTAAATATGAAAA[A/T]ATGTTTATTGGAAAA | 26960 |
rs1031776 | snp | A/G | 0.449473 | 0.150701 | intron-variant | NBEA | GRCh38.p7 | 13:35473237 | CATTTTCTGAGATCT[A/G]TTCTAATGTTTTAAC | 26960 |
rs1033878 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | NBEA | GRCh38.p7 | 13:34959445 | GTAGTATTAATGAGG[C/T]CAAGGAAATGGAATT | 26960 |
rs1065316 | snp | C/T | 0 | 0 | upstream-variant-2KB, missense, intron-variant | NBEA, MAB21L1 | GRCh38.p7 | 13:35475931 | GGCCTCGAGGTCATC[C/T]CCCCCACCGAATTTG | 26960 |
rs1148328 | snp | C/T | 0.142609 | 0.225759 | intron-variant | NBEA | GRCh38.p7 | 13:35078669 | ATTATTCCCAATTAC[C/T]GACTTTTCCATCTCA | 26960 |
rs1148329 | snp | C/T | | | intron-variant | NBEA | GRCh38.p7 | 13:35085822 | atggggttttctaga[C/T]atacaatcatgtcat | 26960 |
rs1148330 | snp | C/G | 0 | 0 | intron-variant | NBEA | GRCh38.p7 | 13:35125862 | tacatacatacataG[C/G]TTctgagaaagaacc | 26960 |
rs1160720 | snp | A/G | 0.362941 | 0.223034 | intron-variant | NBEA | GRCh38.p7 | 13:35312538 | TGAAACTGTGCAAAG[A/G]ATACTGGAGAATAAC | 26960 |
rs1197849 | snp | C/T | 0.370365 | 0.219117 | intron-variant | NBEA | GRCh38.p7 | 13:35356525 | CCATATTTTCCATTG[C/T]TAATCCAATGGGATT | 26960 |
rs1197850 | snp | G/T | 0.421368 | 0.182025 | intron-variant | NBEA | GRCh38.p7 | 13:35356607 | AAATATTCTTCCATA[G/T]TAGAGTGACCGTTGA | 26960 |
rs1197851 | snp | A/T | 0.44546 | 0.155869 | intron-variant | NBEA | GRCh38.p7 | 13:35376772 | AAGGAGATTTAGAGT[A/T]GTAGAGTGTTTAGGA | 26960 |
rs1197852 | snp | A/G | 0.405255 | 0.195948 | intron-variant | NBEA | GRCh38.p7 | 13:35376862 | TGTAAGCCTGCCTCC[A/G]GTTGACCATGTGGTA | 26960 |
rs1197853 | snp | A/G | 0.405429 | 0.195811 | intron-variant | NBEA | GRCh38.p7 | 13:35376875 | CCGGTTGACCATGTG[A/G]TACCCCACTGAGCAG | 26960 |