SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1105398 | snp | C/T | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1399294 | GCACCACCCCACCAT[C/T]CTATCCAAGCCACTT | 9024 |
rs1105470 | snp | A/G | 0.398714 | 0.200958 | intron-variant | BRSK2 | GRCh38.p7 | 11:1404415 | CCTCAGCCTCCCAGG[A/G]CAGACGTCCCTTTGG | 9024 |
rs1109746 | snp | A/G | 0.493107 | 0.0583 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1424005 | ATATAACATAGCCCC[A/G]GATTTGGGGTGGACA | 9024 |
rs1110029 | snp | A/G | 0.4278 | 0.175747 | intron-variant | BRSK2 | GRCh38.p7 | 11:1404146 | CCAGGGCCAGGCTGG[A/G]GGTGCTGTGTGCCCA | 9024 |
rs1316316 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461857 | AGCGAGCCGCACCGT[C/T]TTTAGATGTGTGTGT | 9024 |
rs1317780 | snp | C/G | 0.399432 | 0.200425 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1423098 | CCAGGTACCTCCAGG[C/G]CCCATGCACCCAGGA | 9024 |
rs1554856 | snp | A/C | 0.478354 | 0.101757 | intron-variant | BRSK2 | GRCh38.p7 | 11:1412666 | AGGTTTTCCCACAGA[A/C]ACCTCAGCTCTGCTG | 9024 |
rs1574122 | snp | C/T | 0.396546 | 0.202545 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461258 | TGGGGCCAGGACCCC[C/T]GGTGGGCAACGTAGC | 9024 |
rs1574179 | snp | A/G | 0.478271 | 0.101943 | intron-variant | BRSK2 | GRCh38.p7 | 11:1399839 | GTGTGTCGTGGCTGA[A/G]CCCCAGCTCTGTGGT | 9024 |
rs1881504 | snp | C/G | 0.4941 | 0.0539917 | intron-variant | BRSK2 | GRCh38.p7 | 11:1450056 | TCTTGTGTGTCACTT[C/G]TTTTCTTTTGTGGCT | 9024 |
rs1881505 | snp | A/G | 0.0429648 | 0.14013 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461947 | GCTGCCGCCCGCTAC[A/G]AGACACCGCCCCTCT | 9024 |
rs1881506 | snp | C/T | 0.364193 | 0.222396 | intron-variant | BRSK2 | GRCh38.p7 | 11:1398714 | CCGCATAGGCCTTTC[C/T]CCAGGGCAGCCCTTT | 9024 |
rs1881507 | snp | C/T | 0.21695 | 0.247806 | intron-variant | BRSK2 | GRCh38.p7 | 11:1399049 | GGGGCTGCGGAATGA[C/T]TCCGTCCCTTCCACA | 9024 |
rs1881508 | snp | C/T | 0.378962 | 0.21417 | intron-variant | BRSK2 | GRCh38.p7 | 11:1399327 | GGGGGTTGCTCTTGC[C/T]GGGACTGAGCCCAGG | 9024 |
rs1881509 | snp | A/G | 0.370365 | 0.219117 | intron-variant | BRSK2 | GRCh38.p7 | 11:1404375 | CCACGGGAGGAGGCC[A/G]TCGTCCCAGCCAGCC | 9024 |
rs1881510 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | BRSK2 | GRCh38.p7 | 11:1404680 | AGGGACAGATGCTAA[C/T]GTTTGGGAGGGTAGG | 9024 |
rs1881511 | snp | G/T | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1405018 | GGGGGTTGTAGGGGG[G/T]CTCTCTGAGGGGTGT | 9024 |
rs1973846 | snp | A/G | 0.480144 | 0.097642 | intron-variant | BRSK2 | GRCh38.p7 | 11:1412466 | GAGACTCCACCCACC[A/G]CAGGACGGGGCGGCG | 9024 |
rs2005578 | snp | C/T | 0.333261 | 0.235728 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1423667 | CCCAGCGGGGGAGGC[C/T]TGGGGCAGGGCTTCC | 9024 |
rs2023298 | snp | A/G | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1412202 | ACCGCAGGACGGGGC[A/G]GCGCAGTCAGACTCC | 9024 |
rs2272424 | snp | C/T | 0.346147 | 0.230772 | intron-variant, missense, nc-transcript-variant | BRSK2 | GRCh38.p7 | 11:1450521 | GGCCCGCCTGCCCTG[C/T]GGGTGCCCCCCCGGC | 9024 |
rs2272425 | snp | A/C | 0.0013689 | 0.0261261 | intron-variant, upstream-variant-2KB | BRSK2, LOC105376514 | GRCh38.p7 | 11:1456575 | AGACAGGGGGTTATG[A/C]CCTGGACGGGCCTGG | 9024 |
rs2272426 | snp | C/G | 0.402982 | 0.197728 | intron-variant, nc-transcript-variant | BRSK2, LOC107984298 | GRCh38.p7 | 11:1438469 | CAGCCCCTGTGCTCC[C/G]CAAGCCCCAGACACC | 9024 |
rs2334647 | snp | C/T | 0.383439 | 0.21141 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1422939 | CCAGGTCTGAGAGAC[C/T]TCGAGGTCCATCCTC | 9024 |
rs2334648 | snp | C/G | 0.152334 | 0.230133 | intron-variant | BRSK2 | GRCh38.p7 | 11:1404848 | AGGCAGGCTCGCCGG[C/G]CTGGGGGCAGGGCTC | 9024 |
rs2334655 | snp | A/G | 0.290718 | 0.246662 | intron-variant | BRSK2 | GRCh38.p7 | 11:1396185 | GGTGGAAGGGAAGAG[A/G]GACCAGGAGTGGGGG | 9024 |
rs3081408 | in-del | -/CCC | 0.3748 | 0.216622 | intron-variant | BRSK2 | GRCh38.p7 | 11:1399908 | GCACTCTCCTCTGCT[-/CCC]ATGTGAAAACACCAG | 9024 |
rs3081415 | in-del | -/CGC | | | cds-indel, nc-transcript-variant, upstream-variant-2KB | BRSK2 | GRCh38.p7 | 11:1390003 | cgccgccgccgccgc[-/CGC]CGAggcccgcgcccc | 9024 |
rs3750921 | snp | A/G | 0.0486741 | 0.148216 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461252 | GCCTTCTGGGGCCAG[A/G]ACCCCTGGTGGGCAA | 9024 |
rs3793971 | snp | A/C/G | 0.00466016 | 0.048046 | synonymous-codon, nc-transcript-variant | BRSK2 | GRCh38.p7 | 11:1451375 | TGTGTGCACAGTTCC[A/C/G]ACGCCGGAGGAGATG | 9024 |
rs3817589 | snp | A/G | 0.263233 | 0.24965 | intron-variant | BRSK2 | GRCh38.p7 | 11:1445490 | TCCCGGGTGGGGCAC[A/G]GGGCCTGAGGTGGGA | 9024 |
rs3817590 | snp | C/T | 0.00488707 | 0.04919 | intron-variant | BRSK2 | GRCh38.p7 | 11:1445545 | CCCCGTGTGCCAGCG[C/T]GTCTCGCGCCTCTCG | 9024 |
rs3829225 | snp | C/T | 0.471673 | 0.115589 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461621 | CCCCTGCCGTCTGCG[C/T]GTCTCAGGCAGTGGG | 9024 |
rs3833751 | in-del | -/CT | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461894 | GGGTTCCGTCTCTCT[-/CT]GTGGAGAAGCAGCTC | 9024 |
rs3838784 | in-del | -/G | 0.411437 | 0.190888 | intron-variant | BRSK2 | GRCh38.p7 | 11:1451246 | TGGACCAGTGCCCCT[-/G]GGGGGGCTGTCCCAG | 9024 |
rs3902811 | snp | G/T | 0.170408 | 0.236992 | intron-variant, upstream-variant-2KB | BRSK2, LOC107984298 | GRCh38.p7 | 11:1442817 | GTAGGGGTACAGCCC[G/T]GGCCCTGGCCTGCCT | 9024 |
rs3928714 | snp | C/T | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1412056 | CCGCAGACGGGGCGG[C/T]GCACGTGAGACTCCA | 9024 |
rs3934561 | snp | C/T | 0.489665 | 0.0711382 | intron-variant | BRSK2 | GRCh38.p7 | 11:1403170 | CTTATCCTCGGGGGG[C/T]CTGTGTCACGCTACC | 9024 |
rs4046759 | snp | C/G | 0.262435 | 0.249691 | intron-variant | BRSK2 | GRCh38.p7 | 11:1396181 | GAAGGGAAGAGGGAC[C/G]AGGAGTGGGGGACGT | 9024 |
rs4046760 | snp | C/T | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1396175 | AAGAGGGACCAGGAG[C/T]GGGGGACGTGGGTGG | 9024 |
rs4046908 | in-del | -/GA | 0.403334 | 0.197456 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461887 | TTCTCCACAGAGAGA[-/GA]NCGGAACCCATGACA | 9024 |
rs4072884 | snp | C/T | 0.494568 | 0.0518327 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461490 | AACAGAGACACCCTG[C/T]GGCACCAGAGCCTTC | 9024 |
rs4074034 | snp | C/T | 0.254944 | 0.249951 | intron-variant | BRSK2 | GRCh38.p7 | 11:1400589 | CAGGCGGGCAGGGCA[C/T]TTTGCTGGCCCCGTG | 9024 |
rs4074035 | snp | A/G | 0.481242 | 0.0950111 | intron-variant | BRSK2 | GRCh38.p7 | 11:1400486 | TATACAGGGTCAGGG[A/G]TTATGGAAGAGGTGG | 9024 |
rs4074036 | snp | C/T | 0.477515 | 0.103619 | intron-variant | BRSK2 | GRCh38.p7 | 11:1400473 | GGATTATGGAAGAGG[C/T]GGTCACTGCCCAGGG | 9024 |
rs4079662 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | BRSK2 | GRCh38.p7 | 11:1390763 | CCTATTAGCGCGGCC[A/G]CGGCAGACGGCAGAT | 9024 |
rs4247483 | snp | C/T | 0.41441 | 0.188333 | intron-variant | BRSK2 | GRCh38.p7 | 11:1420518 | AAAAGGGAGCCTGGC[C/T]GTGACGGGGGAACCT | 9024 |
rs4312093 | snp | C/T | 0.369346 | 0.219673 | intron-variant | BRSK2 | GRCh38.p7 | 11:1400259 | GCCCCTGGGAACAGC[C/T]CCCAGCCATGGAGGG | 9024 |
rs4341570 | snp | A/G | 0.162909 | 0.23434 | intron-variant | BRSK2 | GRCh38.p7 | 11:1404233 | CAGGGACACAGCTCC[A/G]CGCACCCAGATTGCG | 9024 |
rs4429085 | snp | C/G | 0 | 0 | intron-variant | BRSK2 | GRCh38.p7 | 11:1412409 | cggggcagcgcagct[C/G]agactccacccaccg | 9024 |
rs4441046 | snp | A/G | 0 | 0 | intron-variant | BRSK2 | GRCh38.p7 | 11:1412418 | ACCGCAGGACGGGGC[A/G]GCGCAGCTCAGACTC | 9024 |
rs4625502 | snp | A/G | 0 | 0 | intron-variant | BRSK2 | GRCh38.p7 | 11:1412408 | ggggcagcgcagctc[A/G]gactccacccaccgc | 9024 |
rs4633454 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1427952 | GAGGGATACCAGGAC[A/G]CAGAGGCCTGCACTG | 9024 |
rs4881746 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | BRSK2 | GRCh38.p7 | 11:1419145 | AAGGCCCCCCCCGCC[A/G]CCAGTGCCCAGACTC | 9024 |
rs4881747 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | BRSK2 | GRCh38.p7 | 11:1393475 | AGGGAGCCCTATCGC[A/G]GCCATTATTCCTTTC | 9024 |
rs4881748 | snp | C/T | 0.152667 | 0.230274 | intron-variant | BRSK2 | GRCh38.p7 | 11:1393350 | GGTTCTCCAGCTCCT[C/T]CCACAGGGCCCTCCC | 9024 |
rs4881749 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | BRSK2 | GRCh38.p7 | 11:1393045 | GCAGCACCTTTGCAG[A/G]TGGGTTCCCACCCCA | 9024 |
rs4881750 | snp | A/C | 0.463989 | 0.129263 | intron-variant | BRSK2 | GRCh38.p7 | 11:1392005 | AGCTGTTTTCTAAAT[A/C]TCTCTCTCAGCACGT | 9024 |
rs4963040 | snp | A/G | 0.181659 | 0.240478 | intron-variant | BRSK2 | GRCh38.p7 | 11:1402389 | TGGCCTTGGGGGTGG[A/G]TGGTCATGGGCAGAG | 9024 |
rs4963041 | snp | A/G | 0.482384 | 0.0921818 | intron-variant | BRSK2 | GRCh38.p7 | 11:1402540 | GCCCCACCCTTCTCC[A/G]GGGACTTGCCCCTCA | 9024 |
rs4963042 | snp | A/G | 0.390651 | 0.206682 | intron-variant | BRSK2 | GRCh38.p7 | 11:1405604 | ATGGGGGACCGACCA[A/G]CGGCGCCAGCTACCC | 9024 |
rs4963043 | snp | A/G | 0.159292 | 0.232964 | intron-variant | BRSK2 | GRCh38.p7 | 11:1420170 | TGCGTGCATGTGTGC[A/G]TGTGTGCATGTGTGA | 9024 |
rs4963044 | snp | C/G | 0.41441 | 0.188333 | intron-variant | BRSK2 | GRCh38.p7 | 11:1420213 | CAGGAAGTGGGGTGG[C/G]CTTGTTAGGATGAGA | 9024 |
rs4963046 | snp | C/G | 0.47934 | 0.0995154 | intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1458755 | AGTAGGGAAGAGGGC[C/G]GAGGAAGAGGGTGCC | 9024 |
rs4963048 | snp | A/G | 0.47596 | 0.106968 | missense, intron-variant, downstream-variant-500B | BRSK2, LOC105376514 | GRCh38.p7 | 11:1460700 | AAGATGGGCCCGCCC[A/G]CCGCCCGCCGCGAGC | 9024 |
rs4963076 | snp | C/T | 0.485866 | 0.0828688 | intron-variant | BRSK2 | GRCh38.p7 | 11:1401946 | GTGGGTCTCTGGTTC[C/T]GTGCTGAGGAGGGGC | 9024 |
rs4963077 | snp | C/T | 0.47852 | 0.101384 | intron-variant | BRSK2 | GRCh38.p7 | 11:1402487 | TCCGGGGAGGAGCAT[C/T]GCAAAGGGTGGGTGG | 9024 |
rs4963078 | snp | A/G | 0.479014 | 0.100263 | intron-variant | BRSK2 | GRCh38.p7 | 11:1414099 | TAAAAGGAAGAGTTT[A/G]CCTTCAAACATAAAG | 9024 |
rs4963079 | snp | C/T | 0.479014 | 0.100263 | intron-variant | BRSK2 | GRCh38.p7 | 11:1414149 | TCAAATTTTTCTGTA[C/T]GAACTAGGATTTGTG | 9024 |
rs4963080 | snp | A/G | 0.478932 | 0.10045 | intron-variant | BRSK2 | GRCh38.p7 | 11:1414623 | attaaaatgaaattc[A/G]cataatataaaatta | 9024 |
rs4963081 | snp | A/G | 0.157311 | 0.232183 | intron-variant | BRSK2 | GRCh38.p7 | 11:1418661 | TTCTTCTCTTTGGAG[A/G]GGGTCCCATTTCCCC | 9024 |
rs4991232 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | BRSK2 | GRCh38.p7 | 11:1401706 | AGTCGGCAAACTCCC[A/T]GCTGTGTCCCCACAG | 9024 |
rs5789214 | in-del | -/CC | 0.49962 | 0.0137727 | intron-variant | BRSK2 | GRCh38.p7 | 11:1453731 | GAGGGCACCACTGAG[-/CC]CCCCAGCCCTGCTGG | 9024 |
rs6578333 | snp | C/G | 0.479095 | 0.100076 | intron-variant | BRSK2 | GRCh38.p7 | 11:1415484 | tgcagcgatttgatt[C/G]tggctcactgcagcc | 9024 |
rs6578384 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | BRSK2 | GRCh38.p7 | 11:1444529 | GGTGGGCCGGGTTCT[C/T]CTGGCTTCAGCTCCC | 9024 |
rs6578412 | snp | C/T | 0.0387552 | 0.1337 | utr-variant-3-prime, nc-transcript-variant, intron-variant | BRSK2, LOC105376514 | GRCh38.p7 | 11:1461352 | CCCCGCCTCCCTGGC[C/T]GCGCCGCCTCCGTGT | 9024 |
rs7101802 | snp | C/T | 0.478932 | 0.10045 | intron-variant | BRSK2 | GRCh38.p7 | 11:1416552 | TTTAACTACCGGCGG[C/T]TGTATTTAGcctcag | 9024 |
rs7101875 | snp | A/G | 0.490563 | 0.0680388 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1424453 | CCAGGCAGACAGTGG[A/G]GGCTGTGTGACCAGT | 9024 |
rs7102167 | snp | C/T | 0.47885 | 0.100637 | intron-variant | BRSK2 | GRCh38.p7 | 11:1416873 | ctcttaaaatgtggc[C/T]tcttcagccaggcgc | 9024 |
rs7102257 | snp | A/C/T | 0.660487 | 0.0468971 | intron-variant | BRSK2 | GRCh38.p7 | 11:1417535 | GGGTCACACTGTGTC[A/C/T]TGCTTCTGTGGGCTG | 9024 |
rs7102279 | snp | C/T | 0.477853 | 0.102875 | intron-variant | BRSK2 | GRCh38.p7 | 11:1413450 | GTCTCTGTCCAGCCC[C/T]GAGGGCCCTGGCAGT | 9024 |
rs7102832 | snp | C/T | 0.47802 | 0.102502 | intron-variant | BRSK2 | GRCh38.p7 | 11:1413913 | CACAGCGCCCAGCTC[C/T]GCCTTCTGCCCCGAG | 9024 |
rs7102838 | snp | C/T | 0.369142 | 0.219784 | intron-variant | BRSK2 | GRCh38.p7 | 11:1413920 | CCCAGCTCTGCCTTC[C/T]GCCCCGAGGAAAATG | 9024 |
rs7103987 | snp | C/T | 0.481932 | 0.0933148 | intron-variant | BRSK2 | GRCh38.p7 | 11:1401564 | TCCTGCAGGCTGCAC[C/T]GAGCCCCTTCGGGCC | 9024 |
rs7105864 | snp | C/T | 0.444533 | 0.157025 | intron-variant, upstream-variant-2KB | BRSK2 | GRCh38.p7 | 11:1409550 | GCTGTGTGGCGTCCG[C/T]GGAAGTTGGTGTCTG | 9024 |
rs7107140 | snp | A/G | 0.431621 | 0.171796 | intron-variant | BRSK2 | GRCh38.p7 | 11:1412906 | TAGTGGCAGTCACTC[A/G]CATGGGACGGGACCG | 9024 |
rs7110854 | snp | C/T | 0.365853 | 0.221536 | intron-variant | BRSK2 | GRCh38.p7 | 11:1448945 | GGCAGGCCTGGTGGG[C/T]AGTGCAGGCCGGGCT | 9024 |
rs7114029 | snp | A/G | 0.373397 | 0.217424 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1424267 | GGCCAGGCGGAGGGA[A/G]GTCTCTGCTGGGTGT | 9024 |
rs7114190 | snp | C/T | 0.0744748 | 0.178019 | intron-variant, downstream-variant-500B | BRSK2, LOC105376516 | GRCh38.p7 | 11:1422055 | GGGGAGGGTGGCGCC[C/T]GTGCCTGGGCTGCAT | 9024 |
rs7114346 | snp | C/T | 0.224412 | 0.248687 | intron-variant, downstream-variant-500B | BRSK2, LOC105376516 | GRCh38.p7 | 11:1422168 | CCCATGAGCCCCTCA[C/T]GGGAGCATGCAGGTG | 9024 |
rs7115782 | snp | C/T | 0.431325 | 0.172108 | intron-variant, upstream-variant-2KB | BRSK2 | GRCh38.p7 | 11:1409560 | GTCCGCGGAAGTTGG[C/T]GTCTGTGCGGTGTGG | 9024 |
rs7117557 | snp | C/T | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1404989 | GGGCGTGCAGGCCTC[C/T]GTCTCTGGTGGTCTA | 9024 |
rs7118115 | snp | A/G | 0.127254 | 0.217792 | intron-variant | BRSK2 | GRCh38.p7 | 11:1396168 | TGTGTGGACCCCTGC[A/G]TCCCCCGCTCCTCGT | 9024 |
rs7120259 | snp | G/T | 0.287867 | 0.247116 | intron-variant, upstream-variant-2KB | BRSK2 | GRCh38.p7 | 11:1408812 | GTGTTTGCCTGTGCT[G/T]GTGTGTGTGTGTGTG | 9024 |
rs7122378 | snp | C/G | 0.281577 | 0.247998 | intron-variant | BRSK2 | GRCh38.p7 | 11:1416528 | TCCAACACGTTCCCC[C/G]GGCTTTCATTTAACT | 9024 |
rs7124503 | snp | G/T | 0.138207 | 0.223612 | intron-variant, upstream-variant-2KB | BRSK2 | GRCh38.p7 | 11:1409673 | AAGGACGCTTTGGGG[G/T]TGTCAGGTATGATGG | 9024 |
rs7126133 | snp | A/G | | | intron-variant | BRSK2 | GRCh38.p7 | 11:1404990 | GGCGTGCAGGCCTCT[A/G]TCTCTGGTGGTCTAG | 9024 |
rs7126241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1425446 | CTGTGGATGAGGCCC[A/G]CTTGGTCCCAGAGGT | 9024 |
rs7127108 | snp | A/T | 0.485392 | 0.0842056 | intron-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1428765 | gatggtatgtgcacg[A/T]gtgtgtgtgcactgc | 9024 |
rs7128873 | snp | A/G | 0.446771 | 0.154211 | intron-variant, nc-transcript-variant | BRSK2, LOC105376516 | GRCh38.p7 | 11:1424132 | CACCATTCCACCCCC[A/G]CATCCTCCAGCTGTG | 9024 |