SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9401 | snp | A/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5620154 | TATTTTTACTACCAG[A/T]AGGTAAAGAAAAAGT | 54476 |
rs710939 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RNF216 | GRCh38.p7 | 7:5651059 | CGGAAGTGAGATATA[C/T]GTATATAATTCCTGT | 54476 |
rs710940 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | RNF216 | GRCh38.p7 | 7:5634204 | AGCCTCCTGTGACCA[C/T]GGGGGAAGAACGGGT | 54476 |
rs710941 | snp | C/T | 0.32885 | 0.23724 | intron-variant | RNF216 | GRCh38.p7 | 7:5633798 | GCAAGCACCCGGCCT[C/T]TCCAGAAACGTGCTG | 54476 |
rs752909 | snp | C/T | 0.217145 | 0.247832 | intron-variant | RNF216 | GRCh38.p7 | 7:5726328 | ACAGGTAAAATCACA[C/T]GACAATGGGCTGGTG | 54476 |
rs752910 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5726355 | GGTGAGTCCCATTCT[A/G]TAGGCAAATCTTCCA | 54476 |
rs852257 | snp | A/G | 0.333722 | 0.235565 | intron-variant | RNF216 | GRCh38.p7 | 7:5700001 | GCCTAAGCTGAAGCT[A/G]CTGTTGGGTGGAATT | 54476 |
rs852258 | snp | A/C | 0.32955 | 0.237006 | intron-variant | RNF216 | GRCh38.p7 | 7:5699759 | CATCACTGCAAGTGG[A/C]ATCAACCACCCAGCC | 54476 |
rs852259 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5698416 | CATGCGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 54476 |
rs852260 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF216 | GRCh38.p7 | 7:5693917 | TAGAACAGTTATTAA[C/T]TTTCGTTGTGTCATT | 54476 |
rs852261 | snp | A/G | 0.253544 | 0.249975 | intron-variant | RNF216 | GRCh38.p7 | 7:5690865 | ATTTTACACATGTGC[A/G]TATGTGTTATTAAGT | 54476 |
rs852262 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RNF216 | GRCh38.p7 | 7:5690585 | GTACAGGGAAAGCAC[C/T]GCTGATGGGAGCTGC | 54476 |
rs852263 | snp | G/T | 0.48 | 0.0979796 | intron-variant | RNF216 | GRCh38.p7 | 7:5689934 | TCTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTCA | 54476 |
rs852264 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | RNF216 | GRCh38.p7 | 7:5689384 | TTCACTTTTCTTCTT[C/G]TTTCTTTTTTTTTTT | 54476 |
rs852265 | snp | C/T | 0.326741 | 0.23793 | intron-variant | RNF216 | GRCh38.p7 | 7:5688906 | GAGTTCAGACTTAAA[C/T]TTTATATTGAAGAAC | 54476 |
rs852266 | snp | C/T | 0.334871 | 0.235153 | intron-variant | RNF216 | GRCh38.p7 | 7:5688368 | GCTGGGCAATTTCCT[C/T]TGACATGCGGTTTGT | 54476 |
rs852267 | snp | C/G | 0.335788 | 0.23482 | intron-variant | RNF216 | GRCh38.p7 | 7:5686934 | gtgagtgagcattac[C/G]acctgagctctgcct | 54476 |
rs852374 | snp | A/G | 0.340108 | 0.233197 | intron-variant | RNF216 | GRCh38.p7 | 7:5636488 | CGAGGGAGTTGTCCC[A/G]TCATGGTTTTGGAGG | 54476 |
rs852375 | snp | C/T | 0.303688 | 0.244167 | intron-variant | RNF216 | GRCh38.p7 | 7:5636069 | CTGGCAGTCTGGATT[C/T]GAGAGTATGGCAAAA | 54476 |
rs852376 | snp | A/G | 0.32955 | 0.237006 | intron-variant | RNF216 | GRCh38.p7 | 7:5635674 | ATTTGTCCTCGGAGT[A/G]TTCCCAGGCCTGCCT | 54476 |
rs852377 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF216 | GRCh38.p7 | 7:5635470 | AGGTATTTTAGACTT[C/T]TAGGTTGGAAACTGA | 54476 |
rs852378 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | RNF216 | GRCh38.p7 | 7:5635078 | tccctagcttggtga[A/G]accaggatgtgagcc | 54476 |
rs852393 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RNF216 | GRCh38.p7 | 7:5682471 | GCAGTAAGACAAGAC[C/T]GCGCCACTGCACTGC | 54476 |
rs852394 | snp | C/T | 0.499997 | 0.00119808 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5681817 | TTTCTGGGTGTTTCC[C/T]GTTTATGTAGTCAGG | 54476 |
rs852395 | snp | C/T | 0.138546 | 0.223781 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680624 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC | 54476 |
rs852396 | snp | C/T | 0.296619 | 0.245615 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680108 | CCCTTGTGTGAAGAA[C/T]GTGGACTTCTTCCTG | 54476 |
rs852397 | snp | C/T | 0.333491 | 0.235646 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679926 | AGGGTCCCTATTGTG[C/T]TTCTTAAAGCCGACT | 54476 |
rs852398 | snp | C/G | 0.030665 | 0.119967 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679186 | CACCACCACCCCTAC[C/G]CGAGGGTGACAGGAT | 54476 |
rs852399 | snp | C/G | 0.030278 | 0.119257 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679129 | TAAATGACTTGATAA[C/G]TAAGATGTTTCATCC | 54476 |
rs852400 | snp | G/T | 0.34101 | 0.232846 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678846 | ACCTTTGCCTCTTAA[G/T]TTATCCAGTCCAGCT | 54476 |
rs852401 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678159 | CAATACTCAGGCATG[G/T]GCCCAAATCTAGGTT | 54476 |
rs852402 | snp | C/G | 0.334871 | 0.235153 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677630 | TCAGATTGGAAAGAA[C/G]TGACTAAGAACAGGT | 54476 |
rs852403 | snp | C/T | 0.17461 | 0.238362 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677218 | TGATTTAGAGACTGC[C/T]CAGCACGTGCTTCTG | 54476 |
rs852404 | snp | C/T | 0.030278 | 0.119257 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677174 | TTAATTCTAATTTGT[C/T]CAGGTGTTAATTTTA | 54476 |
rs852405 | snp | A/G | 0.17654 | 0.238964 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5676414 | ATCATACTTTTTGCA[A/G]CTGCCGTCAGCACTT | 54476 |
rs852406 | snp | A/C | 0.327445 | 0.237702 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5675759 | tcgcaccattgcgtt[A/C]cagcctgggcaacaa | 54476 |
rs852407 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674976 | agagtctctctctgt[C/T]gcccaggctggagtg | 54476 |
rs852408 | snp | G/T | 0.030665 | 0.119967 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674392 | aggcaggcggatcat[G/T]aggtcaggagtttga | 54476 |
rs852409 | snp | C/T | 0.329783 | 0.236927 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673884 | gatagagcaagactc[C/T]gtctcaaaaaaaaaa | 54476 |
rs852410 | snp | A/G | 0.331179 | 0.236453 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673365 | ATGCTTTCTCCCACA[A/G]AGCTATCTCCAGCCC | 54476 |
rs852411 | snp | C/G | 0.186105 | 0.241697 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672775 | CGCAAGGTAGAGGAT[C/G]GATATGAGGGAGGAC | 54476 |
rs852412 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672666 | TGCTTATGTGATCAC[A/G]TAAGTATTTATGCGA | 54476 |
rs852413 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5668895 | TATCTAGTTAGCATA[C/T]TATCCACCTGATGCC | 54476 |
rs852414 | snp | G/T | 0.242201 | 0.249878 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5668267 | cactgcactccagcc[G/T]gggccaacggagcga | 54476 |
rs852415 | snp | C/T | 0.331642 | 0.236293 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5667192 | CCTAGTATTTTTGTT[C/T]TAACTTTAAATCCAC | 54476 |
rs852416 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5665999 | TTTTTGTATTTTTAG[G/T]AGAAACGGGGTTTCA | 54476 |
rs852417 | snp | C/T | 0.353154 | 0.227726 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5664038 | CAAAGATACCTGAGA[C/T]GTACGGTGGTTGATT | 54476 |
rs852418 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5663281 | GTGAACTTTTTTTTA[C/T]TGGATGAATTGAGCC | 54476 |
rs852419 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, downstream-variant-500B | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5662033 | TGGTCTTCTCACACA[A/G]GATGCCATTGTAACC | 54476 |
rs852420 | snp | C/T | 0.342806 | 0.232136 | intron-variant, downstream-variant-500B | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5661960 | ACAGTGACCTGCTTT[C/T]GCTAGCAAACGCCAT | 54476 |
rs852421 | snp | A/C | 0.241627 | 0.24986 | intron-variant | RNF216 | GRCh38.p7 | 7:5661265 | AATAGAGTGAGACCC[A/C]ATCCCTTCGAAAAAC | 54476 |
rs852437 | snp | A/G | 0.0475351 | 0.146656 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5622005 | CCCCTGGCTTTCTGG[A/G]GGAGGAGTGGGCCTC | 54476 |
rs852438 | snp | C/G | 0.25214 | 0.249991 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621780 | CCCTGGGTTTCTAGC[C/G]GTGCCTGAGGCATCA | 54476 |
rs852439 | snp | A/G | 0.0479149 | 0.147179 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621397 | TTGGGAGGCCGAGGC[A/G]GGCGGATGAGTTGAG | 54476 |
rs852440 | snp | A/G | 0.0482946 | 0.147699 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621303 | CCTATAATCCCAGGT[A/G]CTCAGGAGGCTGAGG | 54476 |
rs852441 | snp | C/T | 0.274124 | 0.248833 | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5621055 | GGCAGCCTGCTGCTA[C/T]GTCCTTGCTGGCGCC | 54476 |
rs852442 | snp | A/T | 0.251859 | 0.249993 | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5620426 | GCACTGGGGGTCTTC[A/T]GACCAGCCAGCAAGG | 54476 |
rs852443 | snp | C/T | 0.0322114 | 0.122752 | downstream-variant-500B, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5619754 | TGCAGTCGGTTTCTT[C/T]TGCAGGCCCCTTCCC | 54476 |
rs852448 | snp | A/G | 0.32885 | 0.23724 | intron-variant | RNF216 | GRCh38.p7 | 7:5632838 | TTGGATCCCACTGTG[A/G]TCCATAGGTACACCT | 54476 |
rs852449 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | RNF216 | GRCh38.p7 | 7:5632573 | gccaggctggtctcg[A/T]acccctgacatcagg | 54476 |
rs852450 | snp | A/G | 0.328616 | 0.237317 | intron-variant | RNF216 | GRCh38.p7 | 7:5630930 | CGATTCAGAAACCTG[A/G]GGGGTTATGTGGTTA | 54476 |
rs852451 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | RNF216 | GRCh38.p7 | 7:5630841 | ctcatctgcagcgtg[C/G]caatcagttcatagt | 54476 |
rs852452 | snp | A/G | 0.388964 | 0.20782 | intron-variant | RNF216 | GRCh38.p7 | 7:5630710 | GTCACTGTGCTTGGC[A/G]CTTTATAAGAGTGAT | 54476 |
rs852453 | snp | C/T | 0.304188 | 0.244057 | intron-variant | RNF216 | GRCh38.p7 | 7:5630041 | TGTGTCCTAGATTTG[C/T]AGCGTGGCCTTTTTC | 54476 |
rs852454 | snp | C/T | 0.47709 | 0.104548 | intron-variant | RNF216 | GRCh38.p7 | 7:5628435 | GTTGTATTAAAGTTA[C/T]TAAGCACAGTGTCCT | 54476 |
rs852455 | snp | C/T | 0.189261 | 0.242509 | intron-variant | RNF216 | GRCh38.p7 | 7:5628002 | TCTGTATCAGAAACC[C/T]GGGCTCGCGCTCCTA | 54476 |
rs852456 | snp | A/G | 0.466515 | 0.124985 | intron-variant | RNF216 | GRCh38.p7 | 7:5627783 | GGGGAGAGTCTGAGG[A/G]AAAAAAGGGGGTTAG | 54476 |
rs852457 | snp | A/G | 0.328148 | 0.237472 | intron-variant | RNF216 | GRCh38.p7 | 7:5626985 | TGTTGGTTGTGATTA[A/G]TAACGGACCAGAGTG | 54476 |
rs852458 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RNF216 | GRCh38.p7 | 7:5626226 | GAAGGTAGTAAGTTC[C/T]CCCTTGTGGAGTGTT | 54476 |
rs852459 | snp | C/T | 0.221141 | 0.248329 | intron-variant | RNF216 | GRCh38.p7 | 7:5626149 | CTTATGTGTTAACCC[C/T]GGAGAGAGACAGCTC | 54476 |
rs852460 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | RNF216 | GRCh38.p7 | 7:5625708 | CTGAAGTTTAATCAG[C/T]AAACTTAGAACAGTG | 54476 |
rs852461 | snp | A/C | 0.334182 | 0.235401 | intron-variant | RNF216 | GRCh38.p7 | 7:5624972 | GAGGGGGGTTAAGGT[A/C]AGCGCCACTCATGAA | 54476 |
rs852462 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | RNF216 | GRCh38.p7 | 7:5624426 | CATATCCACCACTTG[A/C]ACGCAGCTCAGTGCA | 54476 |
rs852463 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5647332 | aaaaaaaaaaaaaaa[A/G]aaagaaagaaagaaa | 54476 |
rs852464 | snp | G/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5647073 | gcctcccagtggatt[G/T]tgttgaaagcatttg | 54476 |
rs852465 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | RNF216 | GRCh38.p7 | 7:5645623 | agcgtggggacagag[C/G]aagactctgttgcaa | 54476 |
rs852466 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | RNF216 | GRCh38.p7 | 7:5644570 | tgcagtgagctgata[C/T]tacactactgcactc | 54476 |
rs852467 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | RNF216 | GRCh38.p7 | 7:5644388 | ctataataagatacc[A/G]cttcacacctattag | 54476 |
rs852468 | snp | A/G | 0.325327 | 0.238382 | intron-variant | RNF216 | GRCh38.p7 | 7:5642892 | CCACACCTTAAAGCC[A/G]CACCTCAGCCTCAGG | 54476 |
rs852469 | snp | C/T | 0.202343 | 0.245416 | intron-variant | RNF216 | GRCh38.p7 | 7:5642562 | gctgagacatgtgaa[C/T]cgtttgaacccagga | 54476 |
rs852470 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | RNF216 | GRCh38.p7 | 7:5640661 | AACAATTCTATTAAC[A/G]TAAATCATTATATGG | 54476 |
rs852471 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | RNF216 | GRCh38.p7 | 7:5640222 | ATAAACAAAGATTAG[G/T]GATACATGAAAAACT | 54476 |
rs852472 | snp | A/G | 0.326035 | 0.238157 | intron-variant | RNF216 | GRCh38.p7 | 7:5639852 | gaatggcgtgaaccc[A/G]ggaggcagagcttgc | 54476 |
rs852473 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | RNF216 | GRCh38.p7 | 7:5639461 | aaaaaaTGTGGAGCC[A/G]TGTGTGGTGGCTCAT | 54476 |
rs852474 | snp | A/C | 0.209997 | 0.246779 | intron-variant | RNF216 | GRCh38.p7 | 7:5639183 | ctaaagagcctgctt[A/C]cctatctcttaagga | 54476 |
rs852475 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | RNF216 | GRCh38.p7 | 7:5638813 | acccccatctttaca[A/C]aatatcaaaaattag | 54476 |
rs852476 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RNF216 | GRCh38.p7 | 7:5637720 | AAACTCCATCTCTAC[A/G]AAAAATCCCAAAGTT | 54476 |
rs852477 | snp | A/C | 0.21695 | 0.247806 | intron-variant | RNF216 | GRCh38.p7 | 7:5637711 | CTCTACAAAAAATCC[A/C]AAAGTTATCCAGGGG | 54476 |
rs852514 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | RNF216 | GRCh38.p7 | 7:5659924 | TTAAAATATTAAGAA[G/T]AATAGTAATAAAGTC | 54476 |
rs852515 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RNF216 | GRCh38.p7 | 7:5658425 | ACGTGATCTGCCCAC[A/G]TCGGCTTCCCAGAGT | 54476 |
rs852516 | snp | A/G | 0.252702 | 0.249985 | intron-variant | RNF216 | GRCh38.p7 | 7:5658297 | TATGTTTCATTGTTG[A/G]AATGTTTGGTTTGAG | 54476 |
rs852517 | snp | G/T | 0.371177 | 0.218669 | intron-variant | RNF216 | GRCh38.p7 | 7:5657948 | CACATAACAGCCGAA[G/T]AAGGCTTGGTCCTTG | 54476 |
rs852518 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF216 | GRCh38.p7 | 7:5657698 | ACAACTAGAAGACAC[A/G]GATGGCCTGGAAGCC | 54476 |
rs852519 | snp | A/G | 0.354418 | 0.227615 | intron-variant | RNF216 | GRCh38.p7 | 7:5656494 | CCGTGGTTTCCCCCA[A/G]TCGGAAAGGCACAAG | 54476 |
rs852520 | snp | G/T | 0.273587 | 0.248885 | intron-variant | RNF216 | GRCh38.p7 | 7:5655636 | CTAGCTACATGGTCT[G/T]GTCTTGTCTTTTTTT | 54476 |
rs852521 | snp | C/T | 0.121369 | 0.214369 | intron-variant | RNF216 | GRCh38.p7 | 7:5655392 | CAGGCTGGTCTCTAA[C/T]GTCTGACCTCAGGTG | 54476 |
rs852522 | snp | C/T | 0.263809 | 0.249618 | intron-variant | RNF216 | GRCh38.p7 | 7:5653912 | CTCCAGGGCCATGCT[C/T]ACTGTCTGCAGTCCA | 54476 |
rs852523 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RNF216 | GRCh38.p7 | 7:5652855 | GAGAGAAATTTTTCC[C/T]TGTGCGTCCTTCTAA | 54476 |
rs852524 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNF216 | GRCh38.p7 | 7:5649991 | tgttcaccaggttct[A/G]tctgcatgtcgttca | 54476 |
rs852525 | snp | A/C | 0.040671 | 0.13668 | intron-variant | RNF216 | GRCh38.p7 | 7:5649487 | gtgtcttattctgtc[A/C]tccaggctggaatac | 54476 |
rs860424 | snp | A/G | 0.339656 | 0.233371 | intron-variant | RNF216 | GRCh38.p7 | 7:5636981 | TGGCCTATTCTCAGC[A/G]CTTTTTTCTTTCTTC | 54476 |
rs888582 | snp | C/G | 0.330947 | 0.236533 | intron-variant | RNF216 | GRCh38.p7 | 7:5726987 | CCTGAAAGGCTCCCA[C/G]TCTTCCTTCTTCTCT | 54476 |
rs888583 | snp | C/T | 0.330249 | 0.23677 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712099 | GGAAATCGGTATATG[C/T]AAGGAGTTCTCATTA | 54476 |
rs1035331 | snp | G/T | 0.339203 | 0.233544 | intron-variant | RNF216 | GRCh38.p7 | 7:5729774 | gtcggctccagacag[G/T]tttgtttaacctctc | 54476 |
rs1035332 | snp | C/G | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5728530 | ctggagtgcagtggc[C/G]taatctcggctcact | 54476 |
rs1468996 | snp | A/G | 0.479663 | 0.0987666 | intron-variant | RNF216 | GRCh38.p7 | 7:5694826 | ATGCTTAGCTATTTT[A/G]ACAACACCTAGAACA | 54476 |
rs1833485 | snp | G/T | 0.452719 | 0.146304 | intron-variant | RNF216 | GRCh38.p7 | 7:5779807 | GAGTCTGGCTGTATT[G/T]CCCAGGCTAAAGTGC | 54476 |
rs1968151 | snp | G/T | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5671832 | TGGTGTCTCTCTCTG[G/T]CCttttttttttttt | 54476 |
rs1990835 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | RNF216 | GRCh38.p7 | 7:5721876 | AAACAGATCATTTAC[A/G]TGTCTAATATTTGTT | 54476 |
rs1990836 | snp | A/G | 0.329317 | 0.237084 | intron-variant | RNF216 | GRCh38.p7 | 7:5721521 | CACCAACAAATGGCT[A/G]TAAGCAGCGCTATTC | 54476 |
rs2008415 | snp | C/T | 0.476574 | 0.105661 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5780719 | TTTTACTTTTTTTTT[C/T]TTCTCCTTTTCTTTG | 54476 |
rs2008418 | snp | C/T | 0.0562307 | 0.157967 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5780778 | GGGCCTGGGTAGCAG[C/T]TGTCCTAGGTACTTA | 54476 |
rs2008425 | snp | A/C | 0.0554779 | 0.157039 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5780815 | TTTCTGACAAATCCG[A/C]CAGGGCTCTGTAAAT | 54476 |
rs2009260 | snp | A/G | 0.333261 | 0.235728 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712216 | TGGGCGCGGTGGCTC[A/G]CGCCTGTAGTCCCAG | 54476 |
rs2042110 | snp | C/G | 0.167809 | 0.236103 | intron-variant | RNF216 | GRCh38.p7 | 7:5766170 | CCTGGGTAGCTAAAA[C/G]TATAGGTACATGCCA | 54476 |
rs2112006 | snp | C/T | 0.34437 | 0.231505 | intron-variant | RNF216 | GRCh38.p7 | 7:5746614 | TTGGCTCCAAGATGT[C/T]CTACCTAGCCAATCA | 54476 |
rs2112007 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | RNF216 | GRCh38.p7 | 7:5736768 | cccagatggggtcgc[A/G]gcctggcagaggcgc | 54476 |
rs2112008 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | RNF216 | GRCh38.p7 | 7:5729194 | CATGGAGTGTAATAC[A/C]TTCTAC | 54476 |
rs2161012 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF216 | GRCh38.p7 | 7:5718165 | tcaaactcctgacct[C/T]aagcaatccccccac | 54476 |
rs2161013 | snp | A/G | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5717867 | TGAGCCTGGGAGGTC[A/G]AGGCTGCAGTGAGCT | 54476 |
rs2287591 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | RNF216 | GRCh38.p7 | 7:5725034 | GTTAAGCTTGGGGGG[A/C]AAAACTGGTCTCAAA | 54476 |
rs2287592 | snp | A/G | 0.499137 | 0.0207489 | intron-variant | RNF216 | GRCh38.p7 | 7:5715600 | TCGATAGACCCATTC[A/G]CACTCCTTATGACAA | 54476 |
rs2287593 | snp | G/T | 0.334642 | 0.235236 | intron-variant | RNF216 | GRCh38.p7 | 7:5715562 | ATTCAACTTTTGAAA[G/T]TTTTTTGGGTAACAT | 54476 |
rs2287594 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | RNF216 | GRCh38.p7 | 7:5715459 | ACCATGGGATTGAAT[A/G]TGATAACTTTATATA | 54476 |
rs2287595 | snp | C/T | 0.17654 | 0.238964 | intron-variant | RNF216 | GRCh38.p7 | 7:5715376 | AGGTATGGATTAATA[C/T]TGTGTTAGTATCTTG | 54476 |
rs2302482 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | RNF216 | GRCh38.p7 | 7:5652309 | AAGAACACGCTTGAG[C/T]CACCCCAGTCTGGAg | 54476 |
rs2302907 | snp | C/T | 0.521325 | 0.163886 | intron-variant | RNF216 | GRCh38.p7 | 7:5721229 | AATGGACATGGCTGG[C/T]CCAGGTTCCTAACAC | 54476 |
rs2307941 | in-del | -/CTCCGG | 0.0803434 | 0.183621 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5670995 | CAGAGCAGGCTGCCA[-/CTCCGG]CAGCTCCCCCGGAAC | 54476 |
rs2345666 | snp | C/T | 0.472147 | 0.114677 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5781089 | CGTTTTTCCTCCTCT[C/T]CCCTCACATCTGGAG | 54476 |
rs2345863 | snp | C/T | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5764272 | TACTGTCCAATAGCC[C/T]GTATAGTTTCACCAC | 54476 |
rs2345864 | snp | A/G | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5732920 | ACTCACACGTGGTCA[A/G]CTTCAGTTGGATGAA | 54476 |
rs2345936 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RNF216 | GRCh38.p7 | 7:5707704 | aCCACACACACACAC[A/T]GAAAAGCTTTTTTTT | 54476 |
rs2345937 | snp | C/G | 0.497749 | 0.0334707 | intron-variant | RNF216 | GRCh38.p7 | 7:5706922 | tcaactctttaaatg[C/G]attaaagacttaagt | 54476 |
rs2345938 | snp | A/G | 0.31357 | 0.241783 | intron-variant | RNF216 | GRCh38.p7 | 7:5706872 | aaactagaagaaaac[A/G]taggtggaaagcttc | 54476 |
rs2345939 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | RNF216 | GRCh38.p7 | 7:5706871 | aactagaagaaaacg[C/T]aggtggaaagcttca | 54476 |
rs2537624 | snp | C/T | 0.400504 | 0.199621 | intron-variant | RNF216 | GRCh38.p7 | 7:5642046 | tttcttttttttttt[C/T]tttttttttttttaa | 54476 |
rs2772379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5736837 | GGGTGGCTGCGGGGC[A/G]GAGGGGCTCCTCACT | 54476 |
rs2772388 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF216 | GRCh38.p7 | 7:5736838 | GGGGTGGCTGCGGGG[C/T]GGAGGGGCTCCTCAC | 54476 |
rs2881234 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | RNF216 | GRCh38.p7 | 7:5742261 | ccaggagtttgagac[C/G]agcgtggccaacatg | 54476 |
rs3075700 | in-del | -/TT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5751855 | CTACAAATCTGTTGC[-/TT]TTTTTTTTTTTTTTT | 54476 |
rs3075703 | in-del | -/AT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5721415 | TACACTAGTGACAGG[-/AT]AGGAGATGCCTTCCA | 54476 |
rs3214426 | in-del | -/C | 0.334871 | 0.235153 | intron-variant | RNF216 | GRCh38.p7 | 7:5715609 | GCGCAGACCTCGATA[-/C]GACCCATTCACACTC | 54476 |
rs3735289 | snp | A/G | 0.165527 | 0.235296 | intron-variant, downstream-variant-500B | RNF216, MIR6874 | GRCh38.p7 | 7:5711619 | ACTCACAAAGTACTC[A/G]TCCTCATTTGCTTAT | 54476 |
rs3757478 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | RNF216 | GRCh38.p7 | 7:5721324 | ACCATTTGGGAAGAC[A/T]GGGCTTCTTACCATT | 54476 |
rs3757479 | snp | C/G | 0.4776 | 0.103433 | intron-variant | RNF216 | GRCh38.p7 | 7:5721560 | TCCGCAATTTACCTG[C/G]GAATTGCTAGATCAT | 54476 |
rs3779091 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | RNF216 | GRCh38.p7 | 7:5650229 | GGCTGTTTTTGATTT[C/T]TGGAATCAACATATA | 54476 |
rs3779092 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672969 | CTGAGATGTCCTGGC[C/T]ACAGCTCAGGATCTG | 54476 |
rs3779095 | snp | C/T | 0.166832 | 0.235761 | intron-variant | RNF216 | GRCh38.p7 | 7:5695815 | TGTAAACGGATGTGT[C/T]TATTTATGAACAGTG | 54476 |
rs3779096 | snp | C/T | 0.478188 | 0.10213 | intron-variant | RNF216 | GRCh38.p7 | 7:5697453 | GCAGCTGGTAATGAT[C/T]GTGTTTAGAGGAGAA | 54476 |
rs3801007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF216 | GRCh38.p7 | 7:5684969 | CTTCAGGATGTGCAG[A/G]GGGTATCAGATTTGA | 54476 |
rs3801008 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | RNF216 | GRCh38.p7 | 7:5692570 | GTGCTGCAAGCAGAG[C/G]CCGTGCAGAAGGCGA | 54476 |
rs3801009 | snp | A/G | 0.158632 | 0.232706 | intron-variant | RNF216 | GRCh38.p7 | 7:5692591 | CAGAAGGCGAGCGAG[A/G]AGAAAGGCAGAGCTG | 54476 |
rs3801010 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF216 | GRCh38.p7 | 7:5695587 | AGACAAGTTCTATTG[C/T]CCTTTTATGGTAGAA | 54476 |
rs3801011 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF216 | GRCh38.p7 | 7:5696347 | GAAATTAAGCTTATT[C/T]GACATGCCTTCGGCT | 54476 |
rs3801012 | snp | C/T | 0.117188 | 0.211804 | intron-variant | RNF216 | GRCh38.p7 | 7:5696759 | AGTAATCACAGCAAA[C/T]ACCTGCAACATTGTA | 54476 |
rs3801014 | snp | A/G | 0.007968 | 0.062614 | intron-variant | RNF216 | GRCh38.p7 | 7:5702814 | TGAAGCCTCCTTGCT[A/G]TGACGCCAGCCCTGC | 54476 |
rs3801015 | snp | C/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5703652 | GAAAAGATAAATAAA[C/T]ACAAGTGACATTGGG | 54476 |
rs3801016 | snp | A/C | 0.334412 | 0.235318 | intron-variant | RNF216 | GRCh38.p7 | 7:5704476 | TGAGAAAGGTAAAAG[A/C]GTATGCGCTAATAAC | 54476 |
rs3801017 | snp | C/T | 0.139225 | 0.224118 | intron-variant | RNF216 | GRCh38.p7 | 7:5708739 | GCTGCTGTAAGCTGC[C/T]CAGCTCTTTTTTGGC | 54476 |
rs3801018 | snp | C/T | 0.030278 | 0.119257 | intron-variant | RNF216 | GRCh38.p7 | 7:5710579 | TACTCAATAGGCAAG[C/T]AGACTTTCCTTATAT | 54476 |
rs3801019 | snp | C/T | 0.334412 | 0.235318 | intron-variant | RNF216 | GRCh38.p7 | 7:5710806 | GTAGGCATCACCTCC[C/T]CAGGCAGTCCAACAC | 54476 |
rs3807572 | snp | C/T | 0.431769 | 0.17164 | intron-variant | RNF216 | GRCh38.p7 | 7:5628014 | CCCAGGTTTCTGATA[C/T]AGATCGGCGGGGTCT | 54476 |
rs3807573 | snp | C/T | 0.097727 | 0.198275 | intron-variant | RNF216 | GRCh38.p7 | 7:5629929 | TTCTTGGACTTGGGA[C/T]AAGTGACAGATGGGG | 54476 |
rs3807575 | snp | A/G | 0.119281 | 0.213102 | intron-variant | RNF216 | GRCh38.p7 | 7:5630151 | CTGTCCTGCTGTCTC[A/G]GGGCTGAGTCACAAA | 54476 |
rs3807576 | snp | A/C | 0.338976 | 0.23363 | intron-variant | RNF216 | GRCh38.p7 | 7:5630192 | TGGTGGTAGAGCTGC[A/C]TGGATGGCAGGGTGA | 54476 |
rs3807577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5632155 | GTTCACCTGAACCTA[C/T]TTGAGATCTGAGTTC | 54476 |
rs3807580 | snp | A/G | 0.127944 | 0.218179 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5667868 | TCACTGGATCAGATT[A/G]GGGAAAGGAGCCACT | 54476 |
rs3807581 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669119 | TATCCCACCCAGTCC[C/G]GTGCTATGCAGGATG | 54476 |
rs3807582 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673157 | CAAATGCCCCACCTG[C/T]GGGCAGTACCGCACT | 54476 |
rs3807583 | snp | C/T | 0.179744 | 0.239925 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5676832 | CTTCCTCTCTGGTCA[C/T]TGTCCCAGGCTAGAT | 54476 |
rs3823680 | snp | A/G | 0.147321 | 0.227941 | intron-variant | RNF216 | GRCh38.p7 | 7:5631869 | GATTCCATTGTAGAA[A/G]GTCACGCTCTGCCCC | 54476 |
rs3823681 | snp | C/T | 0.47666 | 0.105476 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669029 | TTTTAGTTCTGTGGA[C/T]CTAATATTATAAAGA | 54476 |
rs3823683 | snp | C/T | 0.334412 | 0.235318 | intron-variant | RNF216 | GRCh38.p7 | 7:5710524 | AGCAACTCATGAAGA[C/T]CCAAGAGGCTGTGCA | 54476 |
rs3837093 | in-del | -/A | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5675492 | ataaatttaaaaaaa[-/A]ttagctgagtgtagt | 54476 |
rs3837094 | in-del | -/G | 0.301429 | 0.244653 | intron-variant | RNF216 | GRCh38.p7 | 7:5690675 | ACAGAAGAGCAAACA[-/G]AAGTCCACAAAGGCA | 54476 |
rs3837095 | in-del | -/GGAA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5693651 | GAAGTAAGAAGGGAA[-/GGAA]CTGTAGGTCTTTTGA | 54476 |
rs3839708 | in-del | -/A | 0.332568 | 0.235971 | intron-variant | RNF216 | GRCh38.p7 | 7:5694436 | TAACATTTGACCTTG[-/A]AAATCCCTGCTTTCC | 54476 |
rs3839709 | in-del | -/A | 0.488905 | 0.0736498 | intron-variant | RNF216 | GRCh38.p7 | 7:5697085 | GGTCTATTTATCTTC[-/A]AAAGTCCTGCTTCCT | 54476 |
rs3857756 | snp | C/T | 0.0678174 | 0.1712 | utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5761138 | TTGCTTCCTTTTCAG[C/T]TCTTTTGAAACAGAT | 54476 |
rs3943984 | snp | A/G/T | 0.0520825 | 0.152737 | intron-variant | RNF216 | GRCh38.p7 | 7:5726007 | TTACAGGTGTGAGCC[A/G/T]CTGCACCCAGCCAAC | 54476 |
rs4263646 | snp | C/T | 0.216649 | 0.247765 | intron-variant | RNF216 | GRCh38.p7 | 7:5766168 | ggtggcatgtaccta[C/T]agttttagctaccca | 54476 |
rs4415230 | snp | C/T | 0.134119 | 0.221521 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5670796 | CATAGCCCAAATTCT[C/T]AGTTCCAGTTATGTG | 54476 |
rs4548062 | snp | C/G | 0.330016 | 0.236849 | intron-variant | RNF216 | GRCh38.p7 | 7:5736514 | gcctcccaaagtgcc[C/G]agatttcagcctctg | 54476 |
rs4720636 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | RNF216 | GRCh38.p7 | 7:5721340 | GGGCTTCTTACCATT[A/T]GCCAACCTACCATCC | 54476 |
rs4720637 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF216 | GRCh38.p7 | 7:5723738 | AAAGGACAGAGGAGG[A/G]AGAACCGTGTCTCAC | 54476 |
rs4720638 | snp | C/G | 0.381697 | 0.212499 | intron-variant | RNF216 | GRCh38.p7 | 7:5723745 | AGAGGAGGGAGAACC[C/G]TGTCTCACTCTTTGA | 54476 |
rs4720639 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | RNF216 | GRCh38.p7 | 7:5756260 | ggccttcccagcaat[A/G]tggaactgtgagtca | 54476 |
rs4720640 | snp | A/G | 0.329084 | 0.237162 | intron-variant | RNF216 | GRCh38.p7 | 7:5757459 | ccttttttccttcct[A/G]acaaaatttttttaa | 54476 |
rs4720641 | snp | G/T | 0.333261 | 0.235728 | intron-variant | RNF216 | GRCh38.p7 | 7:5757805 | atcataattcaggtg[G/T]tatattcattttata | 54476 |
rs4720642 | snp | C/T | 0.329015 | 0.237599 | intron-variant | RNF216 | GRCh38.p7 | 7:5757848 | aactACAGAGGTTGA[C/T]GCATAATAAAAAATT | 54476 |
rs4720643 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | RNF216 | GRCh38.p7 | 7:5763024 | GAAACACAGAAGTTA[G/T]TGATGGGGCCAAAGC | 54476 |
rs4724711 | snp | A/G | 0.18061 | 0.24614 | intron-variant | RNF216 | GRCh38.p7 | 7:5630198 | TAGAGCTGCCTGGAT[A/G]GCAGGGTGAACTCAT | 54476 |
rs4724712 | snp | A/G | 0.499853 | 0.008585 | intron-variant | RNF216 | GRCh38.p7 | 7:5686391 | AGGGGGCTGGGACAG[A/G]AAACAGGATCCCCAT | 54476 |
rs4724713 | snp | A/G | 0.330482 | 0.236691 | intron-variant | RNF216 | GRCh38.p7 | 7:5714614 | GAACAAAATACCACA[A/G]ACTCGGTGGTGTAAA | 54476 |
rs4724714 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | RNF216 | GRCh38.p7 | 7:5720074 | aagaaaacaatgatt[A/G]tgacgatggctctac | 54476 |
rs4724716 | snp | C/T | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5731376 | TATTTAGCTAGCTGC[C/T]AAGCTAGACTGATGA | 54476 |
rs4724717 | snp | G/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5742229 | tttttgtgtttctaa[G/T]agagatggggttttg | 54476 |
rs4724718 | snp | G/T | 0.323671 | 0.238899 | intron-variant | RNF216 | GRCh38.p7 | 7:5745455 | CAACACTATTAAAAT[G/T]TTTGAGGAAGTACCG | 54476 |
rs4724719 | snp | C/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5746876 | TCACTTGAATCCTAA[C/G]ACTCCAAATTACACG | 54476 |
rs4724720 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | RNF216 | GRCh38.p7 | 7:5748071 | ctccataccaatagg[C/G]ggtatcaggcaaata | 54476 |
rs4724721 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | RNF216 | GRCh38.p7 | 7:5750526 | ttgcagcactgttca[C/T]tgagtttttattatc | 54476 |
rs4724722 | snp | C/T | 0.33303 | 0.235809 | intron-variant | RNF216 | GRCh38.p7 | 7:5756596 | gatggggtttcccca[C/T]gttggctaggctggG | 54476 |
rs4724723 | snp | C/T | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5757432 | tgtgtgtgtggctat[C/T]tgcatgatgtacctt | 54476 |
rs4724724 | snp | A/G | 0.479502 | 0.0991411 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768416 | TTGACAGACCTTAAG[A/G]AAGCAAGATGAACCC | 54476 |
rs4724726 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | RNF216 | GRCh38.p7 | 7:5774570 | ATTAACTGTTACCTG[C/T]GAAACAGAAAAATCA | 54476 |
rs4724727 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | RNF216 | GRCh38.p7 | 7:5778440 | TTCTTCAAAGTACTT[A/C]CAACAATACTTTAAT | 54476 |
rs4724729 | snp | A/G | 0.479502 | 0.0991411 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5782456 | TGGGCACAGTGGCTC[A/G]TGTCCATAATCCCCG | 54476 |
rs6463498 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF216 | GRCh38.p7 | 7:5636867 | GCAGTGCATGCTATG[A/G]CACCCAAACAAGGAA | 54476 |
rs6463501 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669910 | aaGTAAGTGAGATTG[C/T]GGATGGTGCGTTTGG | 54476 |
rs6463503 | snp | C/T | 0.159951 | 0.233219 | intron-variant | RNF216 | GRCh38.p7 | 7:5688047 | GATGGAAGGAACTAG[C/T]GACCGCAAATGGAAC | 54476 |
rs6463506 | snp | C/G | 0.331411 | 0.236373 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5713306 | CCTCTAGTTCCTACC[C/G]GCTTCAGAAGGAATT | 54476 |
rs6463507 | snp | C/T | 0.331179 | 0.236453 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5713470 | TGAACAGAGAACTCT[C/T]CAGACCTTTCCTCCC | 54476 |
rs6463508 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | RNF216 | GRCh38.p7 | 7:5735498 | ggaaaataaccaaga[C/G]aattaaaagctaaaa | 54476 |
rs6463509 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | RNF216 | GRCh38.p7 | 7:5736441 | gtgttgcccaggctg[C/G]agtgcagtggcgcga | 54476 |
rs6463511 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | RNF216 | GRCh38.p7 | 7:5738572 | aattagccaggcgtg[C/G]tggcaggcgcctgta | 54476 |
rs6463512 | snp | A/C | 0.0566069 | 0.158427 | intron-variant | RNF216 | GRCh38.p7 | 7:5744815 | CCATCTCTACTAAAA[A/C]TACAAAATTAGCTGG | 54476 |
rs6463513 | snp | A/G | 0.294832 | 0.245947 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5753114 | CTCCTCAAGCAGCCC[A/G]TGCACTTAAGCATTA | 54476 |
rs6463514 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | RNF216 | GRCh38.p7 | 7:5762568 | gtggtgacgggcacc[C/T]gatatcccagctagt | 54476 |
rs6463515 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | RNF216 | GRCh38.p7 | 7:5773161 | GATATTGATGTTATT[A/T]ATAAGTAGCATGGTA | 54476 |
rs6943803 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF216 | GRCh38.p7 | 7:5703922 | AACAGTGAAACTTCT[A/G]ACCCTAAGAATACAT | 54476 |
rs6943875 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | RNF216 | GRCh38.p7 | 7:5717110 | tgtaatcccagcact[C/T]tggaaggccgaggtg | 54476 |
rs6944143 | snp | C/T | 0.325799 | 0.238232 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754668 | TGCACCCGCAGGAAA[C/T]TGTAGATTCCTCTCT | 54476 |
rs6944358 | snp | C/T | 0.416871 | 0.186156 | intron-variant | RNF216 | GRCh38.p7 | 7:5774547 | AAGTGTGACATTGTG[C/T]TATTTTTATTAACTG | 54476 |
rs6944453 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | RNF216 | GRCh38.p7 | 7:5763842 | cttcccaaagtgctg[C/G]gattacaggtgtgaa | 54476 |
rs6944627 | snp | C/T | 0.155325 | 0.23138 | intron-variant | RNF216 | GRCh38.p7 | 7:5763944 | ctgtaatctaagcac[C/T]ttgggaggccgaggc | 54476 |
rs6945345 | snp | G/T | 0.47108 | 0.119691 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674767 | ctaggaggccgaggt[G/T]ggcagatcacctgag | 54476 |
rs6945674 | snp | A/G | 0.0391387 | 0.134304 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783420 | caggagcgagccact[A/G]aacccggccagagga | 54476 |
rs6945676 | snp | A/C | 0.0391387 | 0.134304 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783421 | aggagcgagccacta[A/C]acccggccagaggat | 54476 |
rs6946771 | snp | A/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5626759 | AGCTAAGTGAGCTCG[A/G]CAGGTTCCTGAGTAT | 54476 |
rs6946894 | snp | A/G | 0.148326 | 0.228391 | intron-variant | RNF216 | GRCh38.p7 | 7:5630540 | tgtatcaccatgccc[A/G]gctaatttttaattt | 54476 |
rs6947405 | snp | A/T | 0.0663309 | 0.169604 | intron-variant | RNF216 | GRCh38.p7 | 7:5730245 | TGAAACATAACAAAG[A/T]TGTGCTGATGGACAG | 54476 |
rs6948327 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680324 | GTCATCATAGAATGC[A/G]ATCCACTCCCCCAAG | 54476 |
rs6948331 | snp | A/C/G | 0.0479529 | 0.14742 | intron-variant | RNF216 | GRCh38.p7 | 7:5740498 | tcctccatgcttgat[A/C/G]atgaggtaagctgtt | 54476 |
rs6949086 | snp | C/T | 0.325563 | 0.238307 | intron-variant | RNF216 | GRCh38.p7 | 7:5642606 | ggcatcacaggtgtg[C/T]gccaccacatcacca | 54476 |
rs6950757 | snp | A/G | 0.124837 | 0.216412 | intron-variant | RNF216 | GRCh38.p7 | 7:5698684 | taggcatgagccacc[A/G]ctccggccTCTTGGA | 54476 |
rs6951438 | snp | C/T | 0.293807 | 0.246132 | intron-variant | RNF216 | GRCh38.p7 | 7:5728436 | AATACCAACCAGGCG[C/T]GGTGGTGAGCACCTA | 54476 |
rs6952587 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5740697 | GAACTCAAGGAATTT[A/G]AAAAAAACAAGGGAC | 54476 |
rs6953970 | snp | C/T | 0.4582 | 0.138394 | intron-variant | RNF216 | GRCh38.p7 | 7:5658171 | CATGAGTAATCAGAA[C/T]CTCCATGCAACCAAT | 54476 |
rs6956564 | snp | A/T | 0.168135 | 0.236216 | intron-variant | RNF216 | GRCh38.p7 | 7:5737128 | cagattgttgctgtg[A/T]ctgtgtagaaagaag | 54476 |
rs6956890 | snp | A/G | 0.197703 | 0.244469 | intron-variant | RNF216 | GRCh38.p7 | 7:5686832 | attagactctcataa[A/G]gagtgtgcaactcag | 54476 |
rs6956960 | snp | C/T | 0.29789 | 0.24537 | intron-variant | RNF216 | GRCh38.p7 | 7:5684402 | gcgagccactgcgcc[C/T]ggccCACAAGCTGGG | 54476 |
rs6956990 | snp | C/T | 0.137527 | 0.223271 | intron-variant | RNF216 | GRCh38.p7 | 7:5684460 | ACAAATGCTGATCTT[C/T]AGGCTCCTCTTGGAG | 54476 |
rs6957559 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | RNF216 | GRCh38.p7 | 7:5717328 | attgcactctagccc[A/G]ggcaacaagagtgaa | 54476 |
rs6958272 | snp | C/T | 0.334871 | 0.235153 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754413 | gtgctcctcccacct[C/T]ggcctcccaagaagt | 54476 |
rs6958627 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712019 | TGCTGGCTCTTATCA[A/G]GAAACATAAGCACCA | 54476 |
rs6959488 | snp | A/G | 0.146314 | 0.227484 | intron-variant | RNF216 | GRCh38.p7 | 7:5735472 | aaatataggcaaaga[A/G]caaaactctaggaaa | 54476 |
rs6959871 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF216 | GRCh38.p7 | 7:5742257 | ttgccatgttggcca[C/T]gctcgtctcaaactc | 54476 |
rs6960197 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669750 | tacaaaaattagtcc[A/G]acatggtgttgtgca | 54476 |
rs6960381 | snp | C/G | 0.330482 | 0.236691 | intron-variant | RNF216 | GRCh38.p7 | 7:5760114 | CCTTTTAGCCCAAGT[C/G]TAAATGTGAATTCGA | 54476 |
rs6960897 | snp | C/G | 0.34146 | 0.23267 | intron-variant | RNF216 | GRCh38.p7 | 7:5730331 | GGTAGGTATATAAAT[C/G]ATCAACGTAAAATAT | 54476 |
rs6961803 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5642217 | TCAAGGTTCTGtttt[G/T]tttttttttttttga | 54476 |
rs6963602 | snp | A/G | 0.416871 | 0.186156 | intron-variant | RNF216 | GRCh38.p7 | 7:5776590 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 54476 |
rs6963764 | snp | G/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5682856 | AGGGATCTATTCTAA[G/T]GAATAATTCTAAAAA | 54476 |
rs6964579 | snp | A/G | 0.128288 | 0.218372 | intron-variant | RNF216 | GRCh38.p7 | 7:5734068 | TAGGAGGGGAAAAAA[A/G]TCTCCAACAAACAAT | 54476 |
rs6964645 | snp | A/C | 0.040671 | 0.13668 | intron-variant | RNF216 | GRCh38.p7 | 7:5726864 | ctctgtcttaaaaaa[A/C]aaaaaaaaaaGTGCT | 54476 |
rs6965723 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | RNF216 | GRCh38.p7 | 7:5751490 | tgatcttcctagaaa[C/T]tgaaagaaagagtga | 54476 |
rs6966191 | snp | C/T | 0.067446 | 0.170804 | intron-variant | RNF216 | GRCh38.p7 | 7:5721660 | ttcctccatcagcaa[C/T]gcatgtgagttccag | 54476 |
rs6967635 | snp | G/T | 0.419616 | 0.183658 | intron-variant | RNF216 | GRCh38.p7 | 7:5774302 | TGCGGGTAGGTAGAG[G/T]GGCATGTGCCCAAGT | 54476 |
rs6968103 | snp | A/G | 0.125874 | 0.217008 | intron-variant | RNF216 | GRCh38.p7 | 7:5689212 | AGGTGGATGCTTGAC[A/G]GGGGCAAAGGGCAGG | 54476 |
rs6968987 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5777598 | AAAGTTGACCTAGAC[A/G]CTGAGATCAGGTGAC | 54476 |
rs6969486 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | RNF216 | GRCh38.p7 | 7:5777221 | CTGCTGACAACATGT[C/G]GACCAGAGAAAAATG | 54476 |
rs6969585 | snp | C/G | 0.16846 | 0.236329 | intron-variant | RNF216 | GRCh38.p7 | 7:5737122 | agaaatcagattgtt[C/G]ctgtgtctgtgtaga | 54476 |
rs6971289 | snp | C/T | 0.119978 | 0.213528 | intron-variant | RNF216 | GRCh38.p7 | 7:5656704 | TGTTTTGGCTGTTCA[C/T]GAGGTCTTCACTTTG | 54476 |
rs6971918 | snp | C/T | 0.475437 | 0.108066 | intron-variant | RNF216 | GRCh38.p7 | 7:5761995 | tatcagctaaagaaa[C/T]ctctgtgtgttctcc | 54476 |
rs6971940 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RNF216 | GRCh38.p7 | 7:5649264 | gggcgtggtagcagg[C/T]gcctgtaatcccagc | 54476 |
rs6972718 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5767975 | TTTCATCTAAGATCC[C/T]AGGAGAGCCAAATCT | 54476 |
rs6973104 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | RNF216 | GRCh38.p7 | 7:5740565 | tgccactggaaaatt[G/T]tatttaactgtaaga | 54476 |
rs6973858 | snp | C/G | 0.039522 | 0.134904 | intron-variant | RNF216 | GRCh38.p7 | 7:5654742 | GGCTAGGGTGGGTGG[C/G]GCAGAGAGGAGCTGA | 54476 |
rs6974201 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RNF216 | GRCh38.p7 | 7:5727969 | ATCCTATCTACAGTC[C/T]GTATTTTCCAAACTT | 54476 |
rs6974691 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF216 | GRCh38.p7 | 7:5645708 | tgattctcctgcttc[A/G]gccttccaagtagct | 54476 |
rs6974774 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RNF216 | GRCh38.p7 | 7:5778126 | tcaccatggtgaaac[C/T]gaaatccttaccatg | 54476 |
rs6975280 | snp | A/C | 0.01356 | 0.0812165 | intron-variant | RNF216 | GRCh38.p7 | 7:5623217 | TGGAGAAAAACATTA[A/C]ACCAACCTCAATGGA | 54476 |
rs6975359 | snp | A/G | 0.113334 | 0.209338 | intron-variant | RNF216 | GRCh38.p7 | 7:5625527 | ATGGGCAGCCCCATC[A/G]AGGGCTAACCAACGG | 54476 |
rs6975456 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNF216 | GRCh38.p7 | 7:5623340 | CTGCAAGAAACCAAG[A/G]ACAAATCTGTACTTC | 54476 |
rs6976510 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | RNF216 | GRCh38.p7 | 7:5738390 | accatatgtctggcc[C/T]gtatttatccctttt | 54476 |
rs6977278 | snp | G/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5740696 | TGAACTCAAGGAATT[G/T]GAAAAAAACAAGGGA | 54476 |
rs6977637 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RNF216 | GRCh38.p7 | 7:5637866 | tttctttttctttaa[A/G]atcaagtcttgttct | 54476 |
rs6979003 | snp | G/T | | | intron-variant, downstream-variant-500B | RNF216, MIR6874 | GRCh38.p7 | 7:5711674 | CTTATACATCAGCAG[G/T]CAGGTAAACAGCAGA | 54476 |
rs7455961 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5718647 | cctcgacctcccatg[A/G/T]tcaagcaattctcgt | 54476 |
rs7777650 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5760502 | gcctgggcaatgagt[A/G]aaattccatctcaaa | 54476 |
rs7777831 | snp | A/C | 0.334871 | 0.235153 | intron-variant | RNF216 | GRCh38.p7 | 7:5709275 | ATATGTTCCAGTCTT[A/C]TTTTTCCTCCCCAGA | 54476 |
rs7778761 | snp | G/T | 0.202035 | 0.245356 | intron-variant | RNF216 | GRCh38.p7 | 7:5727492 | agtgctttaggaggt[G/T]gaggtgggaggatag | 54476 |
rs7780518 | snp | C/T | 0.23031 | 0.249223 | intron-variant | RNF216 | GRCh38.p7 | 7:5647111 | gccctgaggaagttg[C/T]gaaaggtgaaaaaaa | 54476 |
rs7781011 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5760236 | AAAACTGTAGAACAg[G/T]ctgggtgcagtggct | 54476 |
rs7782328 | snp | A/G | 0.163564 | 0.234582 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768328 | TGGGTCCAGTAGTGG[A/G]AGGCCGAGGCAGGCA | 54476 |
rs7783367 | snp | A/T | 0.040671 | 0.13668 | intron-variant | RNF216 | GRCh38.p7 | 7:5748730 | agttaagtAGTTATT[A/T]AGTAGTACTAAGTAG | 54476 |
rs7784394 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | RNF216 | GRCh38.p7 | 7:5719352 | ctgcactccagccta[A/G]gtaacacatggagct | 54476 |
rs7784998 | snp | C/T | 0.129664 | 0.219133 | intron-variant | RNF216 | GRCh38.p7 | 7:5758596 | tgtgagatgtggagt[C/T]aaaggaggttatttt | 54476 |
rs7788185 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF216 | GRCh38.p7 | 7:5628681 | cgcccaccaccatat[C/G]tgacttttttttttt | 54476 |
rs7789481 | snp | C/G | 0.135484 | 0.22223 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5753939 | ggcagaggttgcagt[C/G]agctgagatcgcaac | 54476 |
rs7790499 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | RNF216 | GRCh38.p7 | 7:5737813 | TTTACCACCAggctg[A/G]gcacggtggcttatg | 54476 |
rs7791135 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RNF216 | GRCh38.p7 | 7:5628976 | tcgaggtgggtggat[A/G]acttgaggccaggag | 54476 |
rs7793309 | snp | A/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5760067 | TTGCAAAAAATGAAC[A/G]TAAGGATTCTACACC | 54476 |
rs7793632 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF216 | GRCh38.p7 | 7:5760292 | caggctgaggcgggc[A/G]gatcacctgaggtgg | 54476 |
rs7794225 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF216 | GRCh38.p7 | 7:5729893 | ATTTTTTTTCTATTA[C/T]AGAATACGTAAGAGA | 54476 |
rs7794518 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF216 | GRCh38.p7 | 7:5760148 | TAACAGGAAATTTCA[C/G/T]AAACATGTAAGAATG | 54476 |
rs7794571 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNF216 | GRCh38.p7 | 7:5779042 | AGCCACACCATTCCC[A/G]ACTATGTTCTATTAT | 54476 |
rs7794687 | snp | A/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5747776 | aaaaaaaaaaaaaaa[A/G]GGGAAAAAAAAAGAA | 54476 |
rs7794929 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5760415 | cagctactcaggagg[C/T]tcagaccggagaatc | 54476 |
rs7794945 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5760454 | ccaggaggcggagct[C/T]gtggtgagtcgagat | 54476 |
rs7794953 | snp | A/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5760472 | ggtgagtcgagatta[A/C]gccattgcactctgg | 54476 |
rs7795701 | snp | A/G | 0.147656 | 0.228091 | intron-variant | RNF216 | GRCh38.p7 | 7:5748403 | tagctgggattatag[A/G]tgctcaccaccatgc | 54476 |
rs7795811 | snp | A/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5762946 | ATCCCTCTCTTCCTT[A/T]AAAAAGAAGTATCAT | 54476 |
rs7795879 | snp | C/T | 0.111928 | 0.208413 | intron-variant | RNF216 | GRCh38.p7 | 7:5717786 | CAACATTTGGGATTA[C/T]ATTAAATTAtttatg | 54476 |
rs7796461 | snp | A/G | 0.331179 | 0.236453 | intron-variant | RNF216 | GRCh38.p7 | 7:5709320 | TGGGAGCTTCCTCCC[A/G]ATCACATGGTGCTGT | 54476 |
rs7800691 | snp | C/T | 0.334412 | 0.235318 | intron-variant | RNF216 | GRCh38.p7 | 7:5709591 | GCTACATGGCTACCT[C/T]CAAGTTCAGCAGGCC | 54476 |
rs7803308 | snp | C/T | 0.333261 | 0.235728 | intron-variant | RNF216 | GRCh38.p7 | 7:5714390 | cagcctccccagtag[C/T]tgagattataggcat | 54476 |
rs7804319 | snp | C/G | 0.172674 | 0.237741 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5665188 | CAAGCTCACCATGCA[C/G]GGGATTCCTCTCTAT | 54476 |
rs7805039 | snp | C/G | 0.130351 | 0.219509 | intron-variant | RNF216 | GRCh38.p7 | 7:5762483 | caacacggtgaaacc[C/G]catctctactaaaaa | 54476 |
rs7805164 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | RNF216 | GRCh38.p7 | 7:5702367 | AAAAAACTATTTCCA[C/T]AGGGCCAAGCAGAAA | 54476 |
rs7806110 | snp | A/C | 0.110519 | 0.207473 | intron-variant | RNF216 | GRCh38.p7 | 7:5689766 | CAAGACAAGCCTGGC[A/C]TGCGTGGCAAAATTC | 54476 |
rs7807220 | snp | A/G | 0.166832 | 0.235761 | intron-variant | RNF216 | GRCh38.p7 | 7:5773033 | gatccacacgcctca[A/G]cctcccacagtggtg | 54476 |
rs7807655 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RNF216 | GRCh38.p7 | 7:5655064 | CATGGCATTTAGATA[C/G]TTTTTAGCATTCCTG | 54476 |
rs7808644 | snp | C/T | 0.480064 | 0.0978296 | intron-variant | RNF216 | GRCh38.p7 | 7:5773237 | AGTCCTTTTTTTTCC[C/T]CAAATAAGAtttttt | 54476 |
rs7809733 | snp | A/C | 0.153665 | 0.230694 | intron-variant | RNF216 | GRCh38.p7 | 7:5747164 | CTTATAAAACAGAAC[A/C]ACCTGAAAATGTAGC | 54476 |
rs9648578 | snp | C/G | 0.333491 | 0.235646 | intron-variant | RNF216 | GRCh38.p7 | 7:5709856 | ATCTCCTGGGCTCAA[C/G]TGATTGTCCTGCCTC | 54476 |
rs9648579 | snp | A/G | 0.109461 | 0.206758 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712239 | AGTCCCAGCACTTTG[A/G]GAGGCTGAGGTGGGT | 54476 |
rs9691846 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5729650 | GTACATTTCCCATAC[A/G]GGGGAAATCATTTTA | 54476 |
rs9718331 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5737114 | gacacagcaaccatc[C/T]gatttctcaatcttt | 54476 |
rs10089312 | snp | A/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5736619 | CTCACTTTCCAGACT[A/G]GGCAGCCAGGCAGAG | 54476 |
rs10227325 | snp | A/G | 0.140581 | 0.224783 | intron-variant | RNF216 | GRCh38.p7 | 7:5626678 | CTTGTGTTAAAAAAA[A/G]AAAAAAGGAAGAAAG | 54476 |
rs10228732 | snp | A/G | 0.147656 | 0.228091 | intron-variant | RNF216 | GRCh38.p7 | 7:5734681 | TGGGTAATCCAagcc[A/G]ggtgaggtaacacat | 54476 |
rs10229675 | snp | C/T | 0.118584 | 0.212673 | intron-variant | RNF216 | GRCh38.p7 | 7:5773769 | gaagtggttttgtca[C/T]gttggccaggctgat | 54476 |
rs10230002 | snp | C/T | 0.132409 | 0.220618 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678922 | AGCATGGCTGGTTTA[C/T]CAGTTGCTCTCCAAT | 54476 |
rs10231534 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | RNF216 | GRCh38.p7 | 7:5771739 | gaggtggaggttgca[A/G]taggctgtgatcccg | 54476 |
rs10232762 | snp | C/T | 0.297382 | 0.245469 | intron-variant | RNF216 | GRCh38.p7 | 7:5684841 | ACATTTTTAAGGTGA[C/T]GAAAAGAGAGGTCAG | 54476 |
rs10233203 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF216 | GRCh38.p7 | 7:5765136 | GACTAAGAGAGTTTA[C/T]CTCCCACAGATACTC | 54476 |
rs10233472 | snp | A/G | 0 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672250 | TTTATTTTCCATCCA[A/G]AAGAGCACATGGCTT | 54476 |
rs10233615 | snp | C/T | 0.32885 | 0.23724 | intron-variant | RNF216 | GRCh38.p7 | 7:5739744 | AGTGGCTCATGCCTA[C/T]AATCGAAGCACTTTG | 54476 |
rs10236186 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RNF216 | GRCh38.p7 | 7:5631907 | TCCTGCTGCCTTGTA[C/T]GGATTGCTTAGCTCA | 54476 |
rs10239590 | snp | C/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5721015 | AACACACCCCAAGAC[C/G]AGAGCACATCTTCCT | 54476 |
rs10240006 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | RNF216 | GRCh38.p7 | 7:5773849 | TGGGATAACAGGCGA[A/G]TCACCGTGCCTGGCC | 54476 |
rs10240485 | snp | C/G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5633089 | ggttcaagtgattct[C/G/T]ctgcctcagcctccc | 54476 |
rs10241310 | snp | C/T | 0.329262 | 0.238134 | intron-variant | RNF216 | GRCh38.p7 | 7:5717030 | TTGAACAGCAAAGAA[C/T]AGCATCAACAAAAAC | 54476 |
rs10242117 | snp | A/C | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5767524 | cacatacatgcagga[A/C]tagactccccaaaat | 54476 |
rs10242141 | snp | C/T | 0.130351 | 0.219509 | intron-variant, downstream-variant-500B | RNF216, MIR6874 | GRCh38.p7 | 7:5711701 | CAGATATTTGGGCCA[C/T]GAGGGCAGCCCATAA | 54476 |
rs10242661 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712136 | CCCAGGGCACCATGA[C/T]TGTATCTACGGGCCA | 54476 |
rs10247051 | snp | G/T | 0.498059 | 0.0310896 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5780713 | CCGTCTCAAAGAAAA[G/T]GAGAAAAAAAAAAAA | 54476 |
rs10247769 | snp | C/T | 0.111928 | 0.208413 | intron-variant | RNF216 | GRCh38.p7 | 7:5640140 | tcggctccagcgatc[C/T]gcccaccttggcctt | 54476 |
rs10250638 | snp | A/C | 0.134802 | 0.221877 | intron-variant | RNF216 | GRCh38.p7 | 7:5689938 | TCTGTCTCAAACAAA[A/C]AAAAAAAAAGAACAG | 54476 |
rs10250639 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | RNF216 | GRCh38.p7 | 7:5689942 | TCTCAAACAAAAAAA[A/C]AAAAAGAACAGAAAA | 54476 |
rs10252738 | snp | A/G | 0.129664 | 0.219133 | intron-variant | RNF216 | GRCh38.p7 | 7:5766239 | atgttgcagtgagcc[A/G]tgagtgtgccactgc | 54476 |
rs10255883 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | RNF216 | GRCh38.p7 | 7:5700615 | AACTAGTACACAAAA[C/G]CACAAAAAGAGCCAC | 54476 |
rs10256234 | snp | C/T | 0.126564 | 0.217402 | intron-variant | RNF216 | GRCh38.p7 | 7:5642368 | acaggcgcccaccac[C/T]atgcccagctaagtt | 54476 |
rs10257204 | snp | A/G | 0.479824 | 0.098392 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5767510 | TTGTTAACCTATGCC[A/G]CATACATGCAGGACT | 54476 |
rs10258744 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5633082 | cctcccgggttcaag[C/T]gattctcctgcctca | 54476 |
rs10259773 | snp | C/T | 0.334871 | 0.235153 | intron-variant | RNF216 | GRCh38.p7 | 7:5701468 | ATCCTCACTGGGCAG[C/T]TATTACTTCGTGACA | 54476 |
rs10260656 | snp | A/G | 0.120674 | 0.21395 | intron-variant | RNF216 | GRCh38.p7 | 7:5743859 | GAACTGAATCGCAGC[A/G]TGGAGAGTTTAACTC | 54476 |
rs10261277 | snp | A/G | 0.478685 | 0.10101 | intron-variant | RNF216 | GRCh38.p7 | 7:5764785 | AAGAGTAAGGGTAGC[A/G]GCTGGGTGCAGTGGC | 54476 |
rs10263126 | snp | C/T | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5671721 | gaggcaggagaatct[C/T]ttcaaactggaaggc | 54476 |
rs10265842 | snp | C/T | 0.142609 | 0.225759 | intron-variant | RNF216 | GRCh38.p7 | 7:5640080 | tttttttttttttaa[C/T]gagatgggggtctca | 54476 |
rs10267873 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | RNF216 | GRCh38.p7 | 7:5733341 | AGAGGGTCAGCAAGT[A/C]CCTAAAAATAAGTAC | 54476 |
rs10269041 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5633031 | atcgcccaggctgga[A/G]tgcagtggtgcgatc | 54476 |
rs10271741 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF216 | GRCh38.p7 | 7:5775738 | GCCAGGCGTGGTTGC[A/G]GGCACCTGTAGTCCC | 54476 |
rs10272237 | snp | C/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5764553 | ttcaggaggttgagg[C/G]gagagaatcgcttga | 54476 |
rs10272652 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5675195 | ACTACTAACAGTCTG[C/T]TGTATGCTAGTTACT | 54476 |
rs10275016 | snp | C/T | 0.137867 | 0.223442 | intron-variant | RNF216 | GRCh38.p7 | 7:5740287 | gcccgccaccacgcc[C/T]ggctaatttttaatt | 54476 |
rs10275228 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | RNF216 | GRCh38.p7 | 7:5710372 | CTCAAAACTTAAAAA[A/C]AAAAACAAAAACAAA | 54476 |
rs10275238 | snp | A/C | 0.293551 | 0.246177 | intron-variant | RNF216 | GRCh38.p7 | 7:5710378 | ACTTAAAAACAAAAA[A/C]AAAAACAAAAAACGT | 54476 |
rs10276016 | snp | C/T | 0.117886 | 0.21224 | intron-variant | RNF216 | GRCh38.p7 | 7:5735743 | CAATCTATGGCCTGG[C/T]AGTGTACACTCTTAA | 54476 |
rs10276132 | snp | A/G | 0.125182 | 0.216612 | intron-variant | RNF216 | GRCh38.p7 | 7:5698585 | tttgtgtagagacga[A/G]gttgtgctttgttgc | 54476 |
rs10276704 | snp | A/C | 0.39709 | 0.20215 | intron-variant | RNF216 | GRCh38.p7 | 7:5777366 | CAGAGCTCAGATTTT[A/C]TTTTCTAGCCAATGG | 54476 |
rs10277535 | snp | A/T | 0.419776 | 0.18351 | intron-variant | RNF216 | GRCh38.p7 | 7:5772014 | cgaggcgggtggatc[A/T]cctgagctcaggagt | 54476 |
rs10278624 | snp | A/G | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5671819 | tcaaaaaaaaaaaaa[A/G]aaaaaaaaaaggaca | 54476 |
rs10280662 | snp | C/T | 0.128288 | 0.218372 | intron-variant | RNF216 | GRCh38.p7 | 7:5707085 | aagatcagctgatca[C/T]aaatgtgtggattta | 54476 |
rs10281991 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672053 | ccaagacaGTGGCCA[C/T]TGATGACTATCAAGG | 54476 |
rs10441129 | snp | C/T | 0.131381 | 0.220067 | intron-variant | RNF216 | GRCh38.p7 | 7:5737634 | GCTCCAACAGTGTCA[C/T]TGTACAAATTAGAAA | 54476 |
rs10543449 | in-del | -/GTGT | | | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754120 | TTTTTCTTTTGTGTG[-/GTGT]GTGTGTGTGTGTGTG | 54476 |
rs10568093 | in-del | -/TAT | 0.332799 | 0.23589 | intron-variant | RNF216 | GRCh38.p7 | 7:5719055 | GAATAATGTTATTAA[-/TAT]TATTAAGAACCAAGA | 54476 |
rs10568211 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5654713 | aaaaaaaaaaaaaaa[A/G]GGCTCAATCAATGGG | 54476 |
rs10588945 | in-del | -/CA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5748657 | ACACACACACACACA[-/CA]TAATATACTAACTAA | 54476 |
rs10611932 | in-del | -/TTA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5719060 | ATGTTATTAATATTA[-/TTA]AGAACCAAGACTTTT | 54476 |
rs10617479 | in-del | -/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5647351 | TTTTTTTTTTTTTTT[-/T]GAGATAGGGTCTTGC | 54476 |
rs10684747 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5648741 | CAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAGA | 54476 |
rs10693387 | in-del | -/TT | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5668240 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCGC | 54476 |
rs10709023 | in-del | -/T | 0.49941 | 0.0171624 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5767603 | TATTGTTGAGAGGGA[-/T]TTTTTTTTTTTTTTT | 54476 |
rs10713267 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5647329 | CATTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 54476 |
rs10807950 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | RNF216 | GRCh38.p7 | 7:5720144 | TTCTGCTGGTACAAA[C/T]TCAATATGGTGAAAA | 54476 |
rs10951960 | snp | C/T | 0.343924 | 0.231686 | intron-variant | RNF216 | GRCh38.p7 | 7:5746094 | GGAACACAGGAAAAA[C/T]GGCTAACTCCCTTTT | 54476 |
rs10951961 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | RNF216 | GRCh38.p7 | 7:5755648 | CTGTTATAATTCTTT[C/G]TTGTATATAATCCAC | 54476 |
rs11297322 | in-del | -/T | 0.286825 | 0.247273 | intron-variant | RNF216 | GRCh38.p7 | 7:5651657 | TGCATTCTTTTTTTC[-/T]TTTTTTTTTTGAGAC | 54476 |
rs11314929 | in-del | -/T | 0.496314 | 0.0427728 | intron-variant | RNF216 | GRCh38.p7 | 7:5628686 | ACCACCATATCTGAC[-/T]TTTTTTTTTTTTTTT | 54476 |
rs11319565 | in-del | -/A | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5671829 | AAAAAAAAAAAAAAA[-/A]GGACAGAGAGAGACA | 54476 |
rs11387687 | in-del | -/A | 0.147321 | 0.227941 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672714 | GCATGAGTCTGGAAC[-/A]AGAGAAGGCCAGTGA | 54476 |
rs11418751 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | RNF216 | GRCh38.p7 | 7:5774191 | TTAAATCTTGGTTTC[-/A]CCATTTAGTCAATCG | 54476 |
rs11486877 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5688419 | AAGCTTTTTAAAAAA[A/T]TTTAAATGTTCGTAT | 54476 |
rs11509144 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF216 | GRCh38.p7 | 7:5645674 | CAGCTCACTGCAACC[A/T]CCATCTGCCGGGTTC | 54476 |
rs11531468 | snp | A/T | 0.326035 | 0.238157 | intron-variant | RNF216 | GRCh38.p7 | 7:5722650 | ctgcctcggcctccc[A/T]aagtgccaggattac | 54476 |
rs11536475 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | RNF216 | GRCh38.p7 | 7:5722576 | tttgtatttttagta[A/C]agacggggtttcact | 54476 |
rs11556570 | snp | G/T | 0.123798 | 0.215808 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621582 | GCTGCATCAGTCTCC[G/T]GAGTGGCCCGCCACC | 54476 |
rs11560234 | snp | A/G | 0.110519 | 0.207473 | intron-variant | RNF216 | GRCh38.p7 | 7:5744907 | AACCTGGGAGGCAGA[A/G]GTTGCAGTGAGCCAA | 54476 |
rs11561879 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF216 | GRCh38.p7 | 7:5742711 | AGCAATTATCCTGCC[A/G]CAGCCTCCCGAGTAG | 54476 |
rs11761935 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5740300 | cccggctaattttta[A/T]tttttttagtagaga | 54476 |
rs11763027 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | RNF216 | GRCh38.p7 | 7:5750608 | agctggacaaatcta[C/T]gcaaatcgcaaggaa | 54476 |
rs11764855 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF216 | GRCh38.p7 | 7:5745482 | ACCGTAATATAATTA[C/G]ACACGTGAAAGAAGC | 54476 |
rs11770020 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5707889 | cgcaaccacacccag[C/T]taaatttttgtattt | 54476 |
rs11771172 | snp | C/T | 0.278664 | 0.248351 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754589 | CTAGCCATTGGTACA[C/T]GAGGCACAGGAGTCA | 54476 |
rs11772087 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768564 | actgtatgccatgcc[A/G]taacaaattttgaag | 54476 |
rs11971842 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | RNF216 | GRCh38.p7 | 7:5736559 | cgtctgggaagtgag[A/G]agcgtctctgcctgg | 54476 |
rs11971922 | snp | C/T | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5713291 | GGGACATGGGTGGAG[C/T]CTCTAGTTCCTACCC | 54476 |
rs11974054 | snp | A/G | 0.067446 | 0.170804 | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5620557 | GCCCTGTGGTCCCCC[A/G]TGCCTGGCTCGGGGA | 54476 |
rs11975041 | snp | C/T | 0.114036 | 0.209795 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5782563 | caactcttaaaaTAA[C/T]TGCTggccaggcgtg | 54476 |
rs11975614 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF216 | GRCh38.p7 | 7:5722535 | agctgggactacagg[C/T]gcccgccaccatgcc | 54476 |
rs11976271 | snp | G/T | 0.152334 | 0.230133 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5713329 | AAGGAATTGGCTGAC[G/T]CTGAGAGAAATGAGG | 54476 |
rs11976654 | snp | A/G | 0.126219 | 0.217206 | intron-variant | RNF216 | GRCh38.p7 | 7:5658692 | TTTTTTAACTGACTT[A/G]AATAAAGCAGTATAT | 54476 |
rs11977543 | snp | C/T | 0.153997 | 0.230832 | intron-variant | RNF216 | GRCh38.p7 | 7:5755369 | ATACTTAAAAAAAAA[C/T]TGAAAGAATAacaca | 54476 |
rs11977743 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674821 | accaacatggcaaaa[C/T]cccatctctactaaa | 54476 |
rs11977751 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674865 | agctgggcatagtgg[C/T]acgcacctgtaatcc | 54476 |
rs11979543 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | RNF216 | GRCh38.p7 | 7:5638803 | ccacatctggctaat[G/T]tttgatattttgtaa | 54476 |
rs11979546 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | RNF216 | GRCh38.p7 | 7:5714353 | aacctctgcctccca[C/G]attcaaccaattctc | 54476 |
rs11979789 | snp | G/T | 0.137527 | 0.223271 | intron-variant | RNF216 | GRCh38.p7 | 7:5722403 | tgtttgtttTGtttt[G/T]ttttgagacagagtc | 54476 |
rs11980378 | snp | A/G | 0.153332 | 0.230554 | intron-variant | RNF216 | GRCh38.p7 | 7:5645790 | gagaaaggtttcacc[A/G]tgttggccaggctgg | 54476 |
rs11980556 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | RNF216 | GRCh38.p7 | 7:5692764 | TTTAATAATCACATT[C/T]CTATTTTTCAAGTTC | 54476 |
rs11980653 | snp | G/T | 0.154993 | 0.231244 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5753265 | TTTACAAAATTTTCT[G/T]GACTGCCAATTTCTT | 54476 |
rs11981059 | snp | C/T | 0.297382 | 0.245469 | intron-variant | RNF216 | GRCh38.p7 | 7:5733522 | TTCTATGAGGTTAAA[C/T]TGTTAAAAAATACTA | 54476 |
rs11981617 | snp | C/T | 0.138207 | 0.223612 | intron-variant | RNF216 | GRCh38.p7 | 7:5739165 | aataatgtgaattta[C/T]ttaacaacaccaaat | 54476 |
rs11982240 | snp | C/T | 0.00511506 | 0.0503127 | intron-variant | RNF216 | GRCh38.p7 | 7:5714771 | CAAGGTTCTCTCTTT[C/T]TGAGGTAACCTTCCC | 54476 |
rs11982258 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF216 | GRCh38.p7 | 7:5736149 | tgtccctctccccac[A/G]gtctccctctgatgc | 54476 |
rs11984261 | snp | G/T | 0.130351 | 0.219509 | intron-variant | RNF216 | GRCh38.p7 | 7:5762293 | ttagggaggctgagg[G/T]ggatggatcacctaa | 54476 |
rs11984395 | snp | A/G | 0.0556733 | 0.15728 | intron-variant | RNF216 | GRCh38.p7 | 7:5735141 | agagagtgagacttc[A/G]tctcaaaaaaaataa | 54476 |
rs12154413 | snp | C/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5744241 | CTAAAAATACAATAA[C/T]TAATGCTACATATGG | 54476 |
rs12531598 | snp | C/T | 0.329317 | 0.237084 | intron-variant | RNF216 | GRCh38.p7 | 7:5738938 | GAACGAACAAGGTCA[C/T]TAAAAAAGACATAAT | 54476 |
rs12532901 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | RNF216 | GRCh38.p7 | 7:5765914 | gcccagattgcacca[C/T]tgcagtccagcctga | 54476 |
rs12533583 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | RNF216 | GRCh38.p7 | 7:5766706 | gtctatggtatcagt[C/T]agcttgagctgacta | 54476 |
rs12538870 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | RNF216 | GRCh38.p7 | 7:5775058 | GCCTCTTTTCTTACT[C/T]ATAGTTGTATTTCCA | 54476 |
rs12539336 | snp | A/C | 0.348668 | 0.232161 | intron-variant | RNF216 | GRCh38.p7 | 7:5715275 | CTCATCTCTCTGCCA[A/C]CCCCCACACAAATTC | 54476 |
rs12666262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF216 | GRCh38.p7 | 7:5779634 | acccaggagttgggc[A/G]gcacagctagactcc | 54476 |
rs12667079 | snp | A/G | 0.498547 | 0.0269177 | intron-variant | RNF216 | GRCh38.p7 | 7:5772000 | gcactttggaaggcc[A/G]aggcgggtggatcac | 54476 |
rs12668235 | snp | A/G | 0.475525 | 0.107882 | intron-variant | RNF216 | GRCh38.p7 | 7:5779564 | GAATGTTCTGGCAGA[A/G]CACGGTGGCTAAAGC | 54476 |
rs12669801 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF216 | GRCh38.p7 | 7:5645735 | agctgggactacagg[C/T]gcccgccaccacatc | 54476 |
rs12671589 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754885 | atacaaaaattagcc[A/G]ggtgtggtggcatgc | 54476 |
rs12672469 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5769334 | tgttggccaggatgg[G/T]ctcaatctcttgacc | 54476 |
rs12672943 | snp | A/C | 0.499087 | 0.0213463 | intron-variant | RNF216 | GRCh38.p7 | 7:5775953 | ACACCAGGCCTCCAC[A/C]ATACCTCTTCCCAGC | 54476 |
rs12674946 | snp | C/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5736711 | GGCAGAGGCGCTCCC[C/T]ACATCTCAGATGATG | 54476 |
rs13228965 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RNF216 | GRCh38.p7 | 7:5722011 | cactgcagcctcaac[G/T]cctgggctcaggcaa | 54476 |
rs13229546 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | RNF216 | GRCh38.p7 | 7:5722754 | Gggccaggcgcagtg[A/G]ctcacgcctgtaatc | 54476 |
rs13229591 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF216 | GRCh38.p7 | 7:5698665 | tcccaaagtgctgga[A/C]ttataggcatgagcc | 54476 |
rs13230831 | snp | A/C | 0.434398 | 0.168811 | intron-variant | RNF216 | GRCh38.p7 | 7:5732628 | CCTTCATTATGTTTA[A/C]CAACACAACTCTTCT | 54476 |
rs13231407 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768679 | tgttttttttttttt[G/T]gggacagagtcttgc | 54476 |
rs13233396 | snp | A/G | 0.417845 | 0.185278 | intron-variant | RNF216 | GRCh38.p7 | 7:5725933 | TTCATAAACTGGTAC[A/G]GTGGTGGAAGCAAAA | 54476 |
rs13234341 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5687157 | tcccagcactctggg[A/T]ggttgaggtgggcag | 54476 |
rs13235943 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | RNF216 | GRCh38.p7 | 7:5759494 | atcacacttcttttc[C/T]gtagctcactttatt | 54476 |
rs13236200 | snp | C/T | 0.375 | 0.216506 | intron-variant | RNF216 | GRCh38.p7 | 7:5759636 | GTCATTTTTCTTCTT[C/T]TTTTTTTTTTTTTGA | 54476 |
rs13236790 | snp | C/T | 0 | 0 | missense | RNF216 | GRCh38.p7 | 7:5641369 | GGGCAGCAGTCATTT[C/T]TTCTTCACTGAAATA | 54476 |
rs13237614 | snp | G/T | 0.47726 | 0.104176 | intron-variant | RNF216 | GRCh38.p7 | 7:5734471 | aaattattgagctgt[G/T]catctttactttgtt | 54476 |
rs13237895 | snp | C/T | 0.428182 | 0.17536 | intron-variant | RNF216 | GRCh38.p7 | 7:5756855 | cgcccaggctggcct[C/T]gaaatcctaggctca | 54476 |
rs13238598 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5742590 | tggtgaaaaatcttt[C/T]ttttttttttttttt | 54476 |
rs13238618 | snp | A/C | 0.482459 | 0.0919928 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783600 | AGTGTTCCTTCTCTA[A/C]GACAGTAGAGTGTGG | 54476 |
rs13239017 | snp | A/G | 0.475789 | 0.107327 | intron-variant, utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5780279 | TGACCTGGCCAGGCT[A/G]GAGCCAGGTGCATGT | 54476 |
rs13239194 | snp | C/T | 0.435119 | 0.16802 | intron-variant | RNF216 | GRCh38.p7 | 7:5729858 | GCCATCTTCTTTCCA[C/T]ACCATATTTACGAAC | 54476 |
rs13239275 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RNF216 | GRCh38.p7 | 7:5722010 | tcactgcagcctcaa[C/G]tcctgggctcaggca | 54476 |
rs13239620 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5709830 | cgcaatcatggctca[G/T]tgcagcctcaatctc | 54476 |
rs13240446 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768331 | GTCCAGTAGTGGGAG[G/T]CCGAGGCAGGCAAAT | 54476 |
rs13241054 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | RNF216 | GRCh38.p7 | 7:5776079 | TACTAATACAATTAA[C/T]ATTAAATCAATACAG | 54476 |
rs13241373 | snp | C/T | 0.3752 | 0.216391 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783590 | TGCGGCAATGAGTGT[C/T]CCTTCTCTAAGACAG | 54476 |
rs13244423 | snp | C/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5769439 | CTTATTTTAAACAAA[C/G]Aggctgggcgtggtg | 54476 |
rs13246406 | snp | C/T | 0.493658 | 0.0559517 | intron-variant | RNF216 | GRCh38.p7 | 7:5640962 | ATAAAACTGTTAGGG[C/T]ATGCTGCTTTGAGCA | 54476 |
rs13247447 | snp | A/G | 0.460477 | 0.134905 | intron-variant | RNF216 | GRCh38.p7 | 7:5659333 | ATTAACTGACACTAG[A/G]GGCCTAGTCAGAGGA | 54476 |
rs17135681 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RNF216 | GRCh38.p7 | 7:5654921 | TAAGAAACAAACCCT[A/G]TGCCTGACTATTGCA | 54476 |
rs17135721 | snp | A/C/G | 0.0139042 | 0.0824311 | intron-variant | RNF216 | GRCh38.p7 | 7:5731915 | GGTTTGGAGAGGTTC[A/C/G]TTGATTCTGCAGCCC | 54476 |
rs17135724 | snp | A/G | 0.144296 | 0.226554 | intron-variant | RNF216 | GRCh38.p7 | 7:5746368 | TGCAGAGGTCTTTAC[A/G]GCTTGAGTCAAGCCC | 54476 |
rs17135752 | snp | C/G | 0.17138 | 0.237316 | intron-variant | RNF216 | GRCh38.p7 | 7:5763060 | AACTACTGAACTCTG[C/G]GGATAGGAAACAGAG | 54476 |
rs17135757 | snp | A/G | 0.166832 | 0.235761 | intron-variant | RNF216 | GRCh38.p7 | 7:5778005 | AACTGAATCTTCTGT[A/G]ACCAAAGGACATGCT | 54476 |
rs17135759 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RNF216 | GRCh38.p7 | 7:5778247 | AATGGTTCAGTTCCA[C/T]GACTTGCTCCTTCCT | 54476 |
rs17135762 | snp | A/G | 0.395635 | 0.2032 | intron-variant | RNF216 | GRCh38.p7 | 7:5655628 | GGGGGGACAAAAAAA[A/G]ACAAGACCAGACCAT | 54476 |
rs17135763 | snp | G/T | 0.021333 | 0.101051 | intron-variant | RNF216 | GRCh38.p7 | 7:5657864 | GTCAAAGCTCAGGTA[G/T]ATTCAGTGAACTTTC | 54476 |
rs17186478 | snp | G/T | 0.326035 | 0.238157 | intron-variant | RNF216 | GRCh38.p7 | 7:5773117 | CTGACATATATCAGC[G/T]TAAGTTTGGGTCTCT | 54476 |
rs17765559 | snp | C/T | 0.040671 | 0.13668 | intron-variant, downstream-variant-500B | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5662408 | CAACCAGCCCCTGGA[C/T]GCTTACTTGTAAATA | 54476 |
rs28375369 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | RNF216 | GRCh38.p7 | 7:5732741 | ATATCTGCACCCTGG[A/G]GCAAAAGCAGTGGGG | 54476 |
rs28375631 | snp | A/G/T | 0.165474 | 0.238888 | intron-variant | RNF216 | GRCh38.p7 | 7:5731747 | GGTGCTATACCTGCA[A/G/T]TTCTCACACACTTCC | 54476 |
rs28380174 | snp | A/C/G | 0.313684 | 0.248683 | intron-variant | RNF216 | GRCh38.p7 | 7:5732038 | ATCTCTAAGCTCCCC[A/C/G]CTTCCCTACCACCAC | 54476 |
rs28411680 | snp | A/G | 0.139564 | 0.224285 | intron-variant | RNF216 | GRCh38.p7 | 7:5690537 | CTTAGACCAGGGGAG[A/G]AGGCGCCACCTTCAC | 54476 |
rs28417882 | snp | C/T | 0.329317 | 0.237084 | intron-variant | RNF216 | GRCh38.p7 | 7:5633135 | CAGGCGTCCGCCCCA[C/T]GCCCAGCTAATTTTT | 54476 |
rs28418908 | snp | C/T | 0.121717 | 0.214577 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669919 | AGATTGTGGATGGTG[C/T]GTTTGGAAATCCTTT | 54476 |
rs28444267 | snp | C/T | 0.0165899 | 0.089553 | synonymous-codon, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712801 | GGTCTGGGGGAGCAC[C/T]TTCTCCAGCTCACTG | 54476 |
rs28446539 | snp | A/G | 0.123452 | 0.215605 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669617 | GACTGTGTTGGCCAG[A/G]TGCAGTGGTTCACGC | 54476 |
rs28482375 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5748212 | ATCTTAAACCAGTTT[C/T]TGCCAGCTTATAGAG | 54476 |
rs28497392 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5717029 | TTTGAACAGCAAAGA[A/T]TAGCATCAACAAAAA | 54476 |
rs28501214 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5695545 | TCTCCTGCTCTCTCT[C/T]TGCAGAGCAGAAGAC | 54476 |
rs28505204 | snp | A/G | 0.418491 | 0.184691 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5781207 | GGCGGCCTCGGGCCC[A/G]GGGGAGGGAAGCGCG | 54476 |
rs28514378 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5776918 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAAAAAGA | 54476 |
rs28519438 | snp | A/C | 0.0840898 | 0.187013 | intron-variant | RNF216 | GRCh38.p7 | 7:5760530 | AAAAAAAGAAAAAAA[A/C]AAAACAAAACAAAAC | 54476 |
rs28542553 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF216 | GRCh38.p7 | 7:5695498 | GGGTGAGCACGGTTG[C/T]GCCTACTGCTGAGAG | 54476 |
rs28555104 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5776946 | AGAGAGAGAGAGAGA[A/G]AAAAAGAAAGAAAGA | 54476 |
rs28578361 | snp | C/T | 0.128288 | 0.218372 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712465 | GCGACAGAGCGAGAA[C/T]CCACCTCAAAAAAAA | 54476 |
rs28588522 | snp | A/G | 0.125182 | 0.216612 | intron-variant | RNF216 | GRCh38.p7 | 7:5695722 | CCTCGGATGGATGGT[A/G]CACACCAGGCATTCA | 54476 |
rs28590038 | snp | A/G | 0.129664 | 0.219133 | intron-variant | RNF216 | GRCh38.p7 | 7:5764095 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTC | 54476 |
rs28592990 | snp | A/G | 0.268724 | 0.249298 | intron-variant | RNF216 | GRCh38.p7 | 7:5757788 | GATAGAAAATGTTCC[A/G]TATCATAATTCAGGT | 54476 |
rs28602800 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5776920 | AAAAAAAAAAAAAGA[A/G]AGAGAGAAAAAGAGA | 54476 |
rs28642169 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | RNF216 | GRCh38.p7 | 7:5652416 | TCTGTTACTCACATA[C/G]AGGTACGGTACTTGA | 54476 |
rs28673800 | snp | C/T | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5664801 | ACAAAATTCTTTTTT[C/T]TCTTTTTTCTTGAGA | 54476 |
rs28679698 | snp | C/T | 0.114387 | 0.210022 | intron-variant | RNF216 | GRCh38.p7 | 7:5641080 | ATTTTGTTACGTATA[C/T]TCAAAATATTTGTCA | 54476 |
rs28679826 | snp | A/G | 0.161924 | 0.233971 | intron-variant | RNF216 | GRCh38.p7 | 7:5731757 | CTGCAGTTCTCACAC[A/G]CTTCCCTTTCTACTG | 54476 |
rs28691759 | snp | G/T | 0.131723 | 0.220251 | intron-variant | RNF216 | GRCh38.p7 | 7:5632939 | AAGGGTCAAAGCAGA[G/T]AGTGAAACGGGAGTC | 54476 |
rs28706472 | snp | A/G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5776952 | AGAGAGAGAAAAAAA[A/G/T]AAAGAAAGAAAGAAA | 54476 |
rs28707014 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5672767 | GTGAGCAGCGCAAGG[C/T]AGAGGATGGATATGA | 54476 |
rs28720074 | snp | A/G | 0.125182 | 0.216612 | intron-variant | RNF216 | GRCh38.p7 | 7:5695929 | TGCCACAGAAAACAT[A/G]TTTCCCGTCAGAACG | 54476 |
rs28826570 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5748927 | AGATCTGCTTCTCTG[G/T]GTCTCCGTGTCTATA | 54476 |
rs33989516 | in-del | -/T | 0 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5666832 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAT | 54476 |
rs34015908 | in-del | -/A | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5629462 | CTCAGAAAAAAAAAA[-/A]GTGAAGATAACTGAA | 54476 |
rs34017103 | in-del | -/C | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5664169 | TTTTTTGTACTTTCC[-/C]ATGGGCAAAAAAAGC | 54476 |
rs34033957 | in-del | -/A | | | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5782847 | TCAAAAAAAAAAAAA[-/A]TTGCCAAGTACACCT | 54476 |
rs34038766 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5660869 | GCCACCATGCCTGGC[-/C]TGGGGAACATCTTTA | 54476 |
rs34086728 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5707743 | TTTTTTTTTTTTTTG[G/T]GACAGAGTCTCACTC | 54476 |
rs34089106 | in-del | -/T/TT | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5638649 | TTTTTTTTTTTTTTT[-/T/TT]GGGGGGGAGACAGGG | 54476 |
rs34128264 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5701142 | CGTGGCTCTCCCCAG[-/G]TTGCACAGGGCCCTT | 54476 |
rs34158107 | in-del | -/A | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679461 | CACACACCGTAACAA[-/A]GTGTAACGAGGCTGT | 54476 |
rs34171369 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5700116 | CACGGGGACAGGGGG[-/G]TGTTTTCATGCTTGC | 54476 |
rs34172457 | in-del | -/A | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5629849 | AAAAAAAAAAAAAAA[-/A]GAGGGAGGGAGGGTT | 54476 |
rs34179863 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5748099 | TATCAGACCCCTCCC[-/C]TAACTCTGATTTACA | 54476 |
rs34194264 | in-del | -/C | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679224 | GCGGGGGGGCGGTGC[-/C]ACACAGCTAACAAGT | 54476 |
rs34211406 | in-del | -/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5658562 | CTTGGGAGGCTGAGG[-/T]GGGAGGATTTCTTGA | 54476 |
rs34211702 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5762536 | CCCTGCTAATTTTTG[G/T]ATTTTTATTATTTAT | 54476 |
rs34267282 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5756815 | TTATATTTAATTTTT[-/T]GCAGACATGAGAATC | 54476 |
rs34282205 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | RNF216 | GRCh38.p7 | 7:5695162 | ATCCACGGTTCTTCA[A/T]CTGTACAACAAGCAT | 54476 |
rs34287309 | snp | A/C | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674311 | GGGATTACAAGCGTA[A/C]GCCACTGTGCCTAAT | 54476 |
rs34290885 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5620678 | AAATGACCCACCCCT[-/T]GGGGTTTGGCCTTAG | 54476 |
rs34356264 | snp | C/T | 0.169061 | 0.236535 | intron-variant | RNF216 | GRCh38.p7 | 7:5730626 | GTCCCAACAAAGCAC[C/T]TTCTTCCCACAGAGA | 54476 |
rs34462908 | in-del | -/C | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678380 | TAAGGCTGACAGGCC[-/C]TGGGCAGGGAACTAA | 54476 |
rs34504327 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5772794 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 54476 |
rs34505462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5662726 | TCTACTCACAAACAG[A/G]TAACTGTATACTCTG | 54476 |
rs34525497 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5649530 | AGAAAAAAAACGTTT[-/T]GACATCTGGCAGGAT | 54476 |
rs34530431 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5653623 | AAAAAAAAAAAAAAA[-/A]AGAATTAAAAAAAAA | 54476 |
rs34532584 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5724089 | CAAAACTGAGACAGG[-/G]TTTATGACCTGACAG | 54476 |
rs34538947 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5656203 | AACCCAGGAGGTGGA[-/A]GGTTGCATTGAGCTG | 54476 |
rs34564897 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5705994 | GGCCGAAGCAGGTGG[-/G]AGGATTACGAGGTCA | 54476 |
rs34596772 | snp | C/G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5660382 | CTGCAAGCTCTGCCT[C/G/T]TTGGGTTCAAGTGAT | 54476 |
rs34611085 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5660349 | CAGGCTAGAGTGCAG[G/T]GGCGCAATCTCGGCT | 54476 |
rs34613411 | in-del | -/A | 0.406986 | 0.194565 | intron-variant | RNF216 | GRCh38.p7 | 7:5649387 | CTCCGTCTCCAAAGG[-/A]AAAAAAAAAAAGACA | 54476 |
rs34674287 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5660263 | CGGCCCTGTTTTAAA[A/T]TCTTTTTTTTTTTTT | 54476 |
rs34682963 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5735603 | CTAAAAGAACACCCC[-/C]TGAAGAAATCATCCA | 54476 |
rs34706249 | in-del | -/AAC | | | intron-variant | RNF216 | GRCh38.p7 | 7:5730663 | AACAACAACAACAAC[-/AAC]AAAGCACAGCATTTC | 54476 |
rs34759696 | multinucleotide-polymorphism | CT/GG | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5722010 | TCACTGCAGCCTCAA[CT/GG]CCTGGGCTCAGGCAA | 54476 |
rs34782065 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RNF216 | GRCh38.p7 | 7:5656562 | AGCTCCCGCCCTCTC[-/A]GGGGGGAAGGAGCAT | 54476 |
rs34809697 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5774839 | CTCAGTTCACTGCAA[-/A]CATCCCCTCCAGAGT | 54476 |
rs34865088 | snp | A/C | 0.281841 | 0.247964 | intron-variant | RNF216 | GRCh38.p7 | 7:5756890 | ATCCTCCCACTTTGG[A/C]CTTCCAAAGTGCTGG | 54476 |
rs34915284 | in-del | -/A | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5779669 | AAAAAAAAAAAAAAA[-/A]GTTAGCCGAGCGTGG | 54476 |
rs34929591 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5639417 | GTTTTCCTTTTTTTT[-/T]GAGAACCCAAAGTGC | 54476 |
rs34940118 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5703239 | TCTTGTCAACGCTAC[-/T]TTCCTGAATAAAGGT | 54476 |
rs34996643 | in-del | -/A/AAA | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5779844 | AAAAAAAAAAAAAAA[-/A/AAA]AATGCTCAATGAATG | 54476 |
rs35001382 | snp | A/C | 0.0744748 | 0.178019 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5663432 | TAAAAACACAAAAAC[A/C]AATTAGCCAGGTGTG | 54476 |
rs35017142 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5706788 | TAGTAGTCACTTGCC[-/C]TGTTTTTTGCTTTTG | 54476 |
rs35095498 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5686275 | CTCCAAACTCTCAAG[-/A]AACACCACTGCTGCC | 54476 |
rs35107220 | snp | A/C/T | 0.0695222 | 0.173918 | intron-variant | RNF216 | GRCh38.p7 | 7:5722595 | CGGGGTTTCACTGTG[A/C/T]TAGCCAGGATGGTCT | 54476 |
rs35107631 | snp | A/C | 0.16846 | 0.236329 | intron-variant | RNF216 | GRCh38.p7 | 7:5765620 | GGGTGAGAGCGAGAC[A/C]CTGCCTCTGAAACAA | 54476 |
rs35129292 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5650980 | GACATAAAGTCACCC[-/C]AACTACAGGCTACAT | 54476 |
rs35173286 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5689309 | TTACGCTCAGTTTTT[-/T]GTAACCATGACTCAC | 54476 |
rs35188084 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5742121 | TGCGATCTCGGCTCA[-/A]CTGCAACCTCTGCCT | 54476 |
rs35195410 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768298 | GTCGCTATTAGGGGG[-/A]AAAAAAAAAAAAAAG | 54476 |
rs35205113 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5729206 | AATGTATTACACTCC[-/C]ATGTTTTTACGGTCA | 54476 |
rs35211660 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5698674 | GCTGGAATTATAGGC[A/G]TGAGCCACCGCTCCG | 54476 |
rs35221048 | snp | A/G | 0.375 | 0.216506 | intron-variant | RNF216 | GRCh38.p7 | 7:5736452 | GCGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 54476 |
rs35227989 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5735659 | GACTTAGAGACATGG[-/C]AGATTGTGGGAGAAG | 54476 |
rs35235746 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5663573 | TGGGCGACACAGCGA[A/G]ACTCCACCTCAGGAA | 54476 |
rs35248285 | in-del | -/T | 0 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673878 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 54476 |
rs35266141 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5725578 | GTGGCAGCTGGGTGC[-/C]GGTGGCTGACGCCTG | 54476 |
rs35269359 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5698799 | GAGAAACTACACAGG[-/G]AAACCTTCCCTCCTC | 54476 |
rs35288893 | in-del | -/CT/TC | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5755980 | TACTGTCTATAGATT[-/CT/TC]GATATGGTTTGGCTG | 54476 |
rs35302692 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5639276 | ATGACCTCATGTGAT[-/G]CCTTGGCTATGATCT | 54476 |
rs35304255 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5776595 | CAAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 54476 |
rs35309611 | in-del | -/TG | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5757412 | TTGTGTGTGTGTGTG[-/TG]GCTATCTGCATGATG | 54476 |
rs35321519 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | RNF216 | GRCh38.p7 | 7:5730536 | CAGAATTCAAAGTGG[C/T]TCAGACTGGGAGATC | 54476 |
rs35325814 | in-del | -/C | | | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680790 | GGCTCCCCTGTATCC[-/C]TGAAGGACACAGCCA | 54476 |
rs35337338 | snp | A/G | 0.000386091 | 0.0138887 | synonymous-codon | RNF216 | GRCh38.p7 | 7:5623100 | CAGGTTCTGCGGAAC[A/G]GGCCTCGGGAGGGCC | 54476 |
rs35366992 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5681663 | ATTCCTCAACTGGGG[-/G]ATAGTTTTCTGTCTG | 54476 |
rs35370084 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5690006 | TTTGCCGAGTTCACC[-/C]TGTATTATATTTTAC | 54476 |
rs35372254 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5707741 | TTTTTTTTTTTTTTT[-/T]GTGACAGAGTCTCAC | 54476 |
rs35394142 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5736622 | GCCCGGCTGCCCAGT[-/A]CTGGGAAGTGAGGAG | 54476 |
rs35428483 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5761175 | CAGTAAGAATGAGGG[-/G]AGTATCAAAACTCTT | 54476 |
rs35436118 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5696740 | CTTCTGGAAAATGGG[-/A]AAAAGTAATCACAGC | 54476 |
rs35490573 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5626398 | GAGCCAGTGGCAGGC[-/C]TAAGAAAAAAGACTA | 54476 |
rs35508718 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5771524 | ATCCCGGCGGGGTGC[-/C]AGTGGCTCATGCCTG | 54476 |
rs35522289 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5656153 | GGCTTCTGTAATCCC[-/C]AGCTACTCTGGAAGC | 54476 |
rs35607198 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5691092 | ACGGGTTGATCTGCC[-/C]ATGTTTTTAAGTTCC | 54476 |
rs35663886 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF216 | GRCh38.p7 | 7:5651835 | TGTACTTTTAGTAGA[C/G]ATGGGGTTTCACCAT | 54476 |
rs35683428 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5702822 | CTTGCTATGACGCCA[-/A]GCCCTGCTCAGTACG | 54476 |
rs35732993 | snp | C/T | 0.424596 | 0.178931 | intron-variant | RNF216 | GRCh38.p7 | 7:5730699 | AGTGACTGCAAAACA[C/T]GAACATGACACTTGC | 54476 |
rs35786941 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5640580 | AAATACTGTATTTTT[-/T]AAAGCTTAAATCAAG | 54476 |
rs35794405 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5711319 | TACCAGATGTGATGG[-/G]AGATGCCACTAAGAT | 54476 |
rs35798344 | in-del | -/A/AAA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5779829 | AAAAAAAAAAAAAAA[-/A/AAA]AAATGCTCAATGAAT | 54476 |
rs35840113 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5724059 | ATGAAGTTAATGGGA[-/C]AAATGTGAGATGCAG | 54476 |
rs35864920 | in-del | -/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5636879 | TGGCACCCAAACAAG[-/G]GAAAAAGCACATGAG | 54476 |
rs35889050 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754164 | TGTGTGTGTGTGTGC[A/G]CATTTGTCTGGGACA | 54476 |
rs35889722 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF216 | GRCh38.p7 | 7:5730917 | AGTCCTTAGTCACAC[A/G]TTACAACTGGCCTAT | 54476 |
rs35890223 | snp | A/C | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5645802 | ACCATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT | 54476 |
rs35905773 | in-del | -/A | 0 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5663608 | AAAAAAAAAAAAAAA[-/A]GTTCACTTGAGGCCG | 54476 |
rs35911777 | in-del | -/TG | 0 | 0 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754161 | GTGTGTGTGTGTGTG[-/TG]CGCATTTGTCTGGGA | 54476 |
rs35940234 | in-del | -/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5683025 | CGGGGTCACAAACTC[-/C]TTAAGAATGCAGAAA | 54476 |
rs35984590 | multinucleotide-polymorphism | GT/TC | | | intron-variant | RNF216 | GRCh38.p7 | 7:5730891 | GCTTCAAATGCAATG[GT/TC]TGAAGAATATAGTCC | 54476 |
rs36009601 | in-del | -/AATC | | | intron-variant | RNF216 | GRCh38.p7 | 7:5707787 | GGAGTACAGCGGCAC[-/AATC]TCTGCTCACCGCAAC | 54476 |
rs36009719 | snp | C/T | 0.093417 | 0.194889 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5780752 | AAAAAGAACGTTCTC[C/T]TTGCACGATCTAAGT | 54476 |
rs36015761 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5749805 | GAAACTAATGGATTT[-/T]GTGTAACTGCTAACC | 54476 |
rs36033441 | snp | A/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5629528 | ATCTTATGCTTCACC[A/C]CAATTAAAAAGAGGG | 54476 |
rs36078723 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RNF216 | GRCh38.p7 | 7:5714528 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 54476 |
rs36088177 | multinucleotide-polymorphism | AC/GT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5706871 | TGAAGCTTTCCACCT[AC/GT]GTTTTCTTCTAGTTT | 54476 |
rs36099512 | in-del | -/T | 0.394904 | 0.203722 | intron-variant | RNF216 | GRCh38.p7 | 7:5659971 | AATTACATTCATTAA[-/T]TTTTTTTTTTTTTTT | 54476 |
rs36102190 | in-del | -/T/TT | 0.137527 | 0.223271 | intron-variant | RNF216 | GRCh38.p7 | 7:5722369 | CATGTTTTTTTTTTT[-/T/TT]GTTTGTTTGTTTGTT | 54476 |
rs55642870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5781246 | GGCTGTTGCCCTCGC[A/G]CAGCAGACCCGAGGG | 54476 |
rs55645443 | in-del | -/AAACAAAACA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5705959 | AAACAAAACAAAACA[-/AAACAAAACA]CCACTCTGGGAGGCC | 54476 |
rs55678664 | snp | A/G | 0.167158 | 0.235875 | intron-variant | RNF216 | GRCh38.p7 | 7:5771669 | CCAGGCGCAGTAGCG[A/G]GCACCTAGTCCCAGC | 54476 |
rs55685905 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5761299 | CCACACAAACTCAAA[A/G]CCTATGACATTAAAA | 54476 |
rs55690035 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF216 | GRCh38.p7 | 7:5683967 | TACTGCTAAGTTAAG[A/G]GCAAGATCCAGTAGG | 54476 |
rs55757850 | snp | C/T | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5668464 | TCCTGACCTCGTGAT[C/T]TGCCCGCCTCGGCCT | 54476 |
rs55763392 | snp | C/T | 0.39325 | 0.204889 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5781731 | AACCATAGAGGCACT[C/T]CGGGTACTGCGGAGG | 54476 |
rs55820126 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5760600 | GGCTAAGCCAGAATC[C/T]TCTGGCAAAAAAGAA | 54476 |
rs55832875 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5762189 | TACCATTTATGTAAG[C/T]TAATAC | 54476 |
rs55841950 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF216 | GRCh38.p7 | 7:5650344 | TGTGGCAGACCAAGA[C/T]GCTGAGCGGAACCAG | 54476 |
rs55851619 | snp | A/T | 0.0663309 | 0.169604 | intron-variant | RNF216 | GRCh38.p7 | 7:5644533 | TTTTTTGAGACAGAG[A/T]CTCACTCTGTCATCC | 54476 |
rs55873551 | snp | A/T | 0.228842 | 0.249103 | intron-variant | RNF216 | GRCh38.p7 | 7:5723655 | CCGTCTCAAAAAAAA[A/T]AAATAAATAAATAAA | 54476 |
rs55943759 | in-del | -/A/AA/AAA | 0.453697 | 0.14494 | intron-variant | RNF216 | GRCh38.p7 | 7:5745893 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAGCAACGAGAACAC | 54476 |
rs55976102 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | RNF216 | GRCh38.p7 | 7:5771864 | AACAACGGCTGAGTA[A/C]CCCGAGGAAACGCAA | 54476 |
rs56046509 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | RNF216 | GRCh38.p7 | 7:5625372 | TATTTTCCTAGACAC[C/G]GCGTCAGAGCCTAAA | 54476 |
rs56062921 | snp | C/T | 0.416708 | 0.186302 | intron-variant | RNF216 | GRCh38.p7 | 7:5776358 | GGAGGCCAAGGCGGG[C/T]GGATCACGAGGTCAG | 54476 |
rs56129235 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5717151 | CTGAGATCAGGAGTT[C/T]GAGACCAGCCTGACC | 54476 |
rs56145422 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5775504 | ATATGCCTGCCACTT[C/T]TGCAACAGATTTGGG | 54476 |
rs56167942 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5658540 | GTATGTGCCTGTAGT[C/T]TCAGCTACTTGGGAG | 54476 |
rs56364996 | snp | A/G | 0.158302 | 0.232576 | intron-variant | RNF216 | GRCh38.p7 | 7:5714501 | GACCTCAGGTGATCC[A/G]CCTACCTCGGCCTCC | 54476 |
rs56390377 | snp | C/T | 0.168135 | 0.236216 | intron-variant | RNF216 | GRCh38.p7 | 7:5764591 | AGGCGGAGGTTGCAG[C/T]AGGCCAAGATTGTGC | 54476 |
rs56391533 | snp | C/G | 0.130008 | 0.219321 | intron-variant | RNF216 | GRCh38.p7 | 7:5634738 | TGTTTTGCGTCCCGT[C/G]AGGGTCAAGTGCTCA | 54476 |
rs56400876 | in-del | -/AAAAT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5738729 | AAAAAAAAAAAAAAA[-/AAAAT]GCTTCCATGTATTTC | 54476 |
rs56894423 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5706239 | AAAAAAAAAAAAAAA[-/A]TTGTGGTGAAAACAC | 54476 |
rs56903968 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5765806 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCGTGGC | 54476 |
rs56984603 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | RNF216 | GRCh38.p7 | 7:5623527 | CTGGTCTCAAACTCC[C/T]GGGCTCAACTGATCC | 54476 |
rs57001326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF216 | GRCh38.p7 | 7:5742492 | TAGTAACTAGCAAAA[C/T]GAAAAATTAAAACAA | 54476 |
rs57024697 | in-del | -/ACT | 0.0558544 | 0.157504 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679740 | AGAAAGGCAGGCACC[-/ACT]GAGAGAAGAGCGTAT | 54476 |
rs57103271 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | RNF216 | GRCh38.p7 | 7:5658819 | ACAAATAAACACATA[C/T]GCTGGGGGTGTCCTC | 54476 |
rs57302110 | snp | A/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5658675 | AAAAAAAAAAAAAAA[A/T]TTTTTTTAACTGACT | 54476 |
rs57308117 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5693242 | TACTTTCACGCTATA[A/G]AGGCAGAGTTAGGTA | 54476 |
rs57309152 | snp | C/T | 0.111576 | 0.20818 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5671600 | AAGAGGTCAGCAGTT[C/T]GAGACCAGCCTGACC | 54476 |
rs57360981 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5633049 | CAGTGGTGCGATCTC[G/T]GCTCACTGCAACCTC | 54476 |
rs57431557 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF216 | GRCh38.p7 | 7:5683692 | GACAATGTCAGCACC[C/T]TCCTCTCAGGGTTAC | 54476 |
rs57441742 | snp | A/C | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680231 | CTCTTCCGGAAGTCT[A/C]TTCATGCTCTAATGC | 54476 |
rs57712206 | snp | A/G | 0.146314 | 0.227484 | intron-variant | RNF216 | GRCh38.p7 | 7:5742632 | ACAGAGTCTCGCTCT[A/G]TTGCCCAGGCTGGAG | 54476 |
rs57742641 | in-del | -/T | 0.0562307 | 0.157967 | intron-variant | RNF216 | GRCh38.p7 | 7:5750936 | GATGGCGCTTCTTGC[-/T]TGCACACAGATAAAA | 54476 |
rs57807609 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5657887 | GAACTTTCTTTCCTT[C/T]TACTAAGGGAATCCA | 54476 |
rs57849498 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673158 | AAATGCCCCACCTGC[A/G]GGCAGTACCGCACTG | 54476 |
rs57926060 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RNF216 | GRCh38.p7 | 7:5627225 | ACAAACACACACACC[A/G]GGCCACTCAATGGTC | 54476 |
rs57948142 | snp | A/G | 0.16976 | 0.236773 | intron-variant | RNF216 | GRCh38.p7 | 7:5748191 | CTGATGAACTACTAC[A/G]TATAGATCTTAAACC | 54476 |
rs57984156 | in-del | -/A/AA | 0.148326 | 0.228391 | intron-variant | RNF216 | GRCh38.p7 | 7:5707688 | TCTTAGTAAAAAAAA[-/A/AA]GCTTTTCAGTGTGTG | 54476 |
rs58070134 | in-del | -/TATGA | 0.129664 | 0.219133 | intron-variant | RNF216 | GRCh38.p7 | 7:5706947 | AGTTGATTTTTGTGT[-/TATGA]TATGAGATATGGTAT | 54476 |
rs58145592 | snp | C/G | 0.134119 | 0.221521 | intron-variant | RNF216 | GRCh38.p7 | 7:5627865 | GCCCCCTGTGGCACT[C/G]CTGAGGCTGAGAGCA | 54476 |
rs58341461 | in-del | -/GGAA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5755266 | GAAGGAAGGAAGGAA[-/GGAA]CCTATCACCTTATAA | 54476 |
rs58357556 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF216 | GRCh38.p7 | 7:5657528 | GCCGAAATCTTGCCA[C/T]TGCACTCCAGCCTGG | 54476 |
rs58363330 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5702906 | TTTACCATCACCTGA[C/G]TTTAAGCCAGTGTCT | 54476 |
rs58364611 | snp | C/T | 0.115438 | 0.210697 | intron-variant | RNF216 | GRCh38.p7 | 7:5778394 | ATCCCCTAGATGTTC[C/T]TCCCTGGTTCAATCA | 54476 |
rs58373848 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5666647 | GAGCTCTCAAGCCTT[A/C]TGAGCTGCGCCTCTG | 54476 |
rs58408506 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5689529 | AAACAAAAAACCCTA[G/T]GCTTGTAGTCAAGTA | 54476 |
rs58469547 | snp | A/G | 0.139903 | 0.224452 | intron-variant | RNF216 | GRCh38.p7 | 7:5694737 | ATTCTCTGTAGCTGC[A/G]TAGCTTGTGTTGGGC | 54476 |
rs58472634 | in-del | -/TT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5648120 | CTATTTTTTTTTTTT[-/TT]CTTGAGATGGAGTTT | 54476 |
rs58503972 | snp | A/G | 0.105569 | 0.204058 | intron-variant | RNF216 | GRCh38.p7 | 7:5745613 | TTAATGTAAAAAGCA[A/G]CAAGGGCAGGGCACG | 54476 |
rs58562307 | snp | A/G | 0.148996 | 0.228688 | intron-variant | RNF216 | GRCh38.p7 | 7:5627626 | GTGGTACACGCCTAT[A/G]ATCCCAGCTACTCGG | 54476 |
rs58571278 | snp | A/G | 0.0397356 | 0.135236 | intron-variant | RNF216 | GRCh38.p7 | 7:5729624 | AGAAGCATAAAATCA[A/G]AGGCCAGGCAGTACA | 54476 |
rs58579662 | in-del | -/ATACA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5758308 | CACTACCAAGTTAGA[-/ATACA]TTATTAATAAAATCC | 54476 |
rs58797144 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, downstream-variant-500B | RNF216 | GRCh38.p7 | 7:5652133 | AAGTTAATTAAAACG[C/T]GTTACTTGCTTATTT | 54476 |
rs58818900 | in-del | -/CACA/CACACACA | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5698415 | ACACACACACACACA[-/CACA/CACACACA]TACACACACACGCAT | 54476 |
rs58929486 | in-del | -/TTTTTTT | 0.147321 | 0.227941 | intron-variant | RNF216 | GRCh38.p7 | 7:5715737 | ATCACCAACTCATTC[-/TTTTTTT]TTTTTTTTTTTTTTT | 54476 |
rs59052517 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754159 | GTGTGTGTGTGTGTG[-/TGTG]CGCATTTGTCTGGGA | 54476 |
rs59086001 | snp | A/T | 0.118584 | 0.212673 | intron-variant | RNF216 | GRCh38.p7 | 7:5645857 | AGCCTCCCAAAGTGC[A/T]GGGATTACAGGCGTG | 54476 |
rs59107853 | snp | G/T | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5676027 | TTCTTTTTTCTTTTT[G/T]TTTTTGAGACAGAGT | 54476 |
rs59152032 | in-del | -/A | 0.356597 | 0.226135 | intron-variant | RNF216 | GRCh38.p7 | 7:5631669 | GGTTCTCATCAACAT[-/A]AAAAAAAAAATGCCA | 54476 |
rs59217891 | snp | C/G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5732424 | TCTACATGAAATACA[C/G/T]ATGGAACAGTAGATA | 54476 |
rs59222276 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5686138 | TGAGGCAGGAGAATC[G/T]CTTGAATCCAGAAGG | 54476 |
rs59390560 | in-del | -/CTTCT/CTTTT/CTTTTTT | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5759635 | GTCATTTTTCTTCTT[-/CTTCT/CTTTT/CTTTTTT]TTTTTTTTTTTTTTG | 54476 |
rs59440013 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5644842 | TTTTTTTTTTTTTTT[-/T]GAAACGGAGTCTTGC | 54476 |
rs59475900 | in-del | -/AGAAAGGAAGGAAGGGAGGGAAGGA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5755212 | GAAGGGAGGGAAGGA[-/AGAAAGGAAGGAAGGGAGGGAAGGA]TGAAAGGAAGGAAGG | 54476 |
rs59495898 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5706884 | CTACGTTTTCTTCTA[A/G]TTTTTATAGTTTCAG | 54476 |
rs59518633 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5713765 | AGACGACATTTTAAA[A/C]ATAACTAGCTAAAAT | 54476 |
rs59545890 | in-del | -/TT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5742612 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGC | 54476 |
rs59608453 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5753457 | AATCATTTAAGCAAA[C/T]CTATGTCAATGCTTT | 54476 |
rs59658124 | in-del | -/CACA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5748655 | ACACACACACACACA[-/CACA]TAATATACTAACTAA | 54476 |
rs59691320 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF216 | GRCh38.p7 | 7:5649229 | AAACCCCATCTCTAC[C/T]AAAAATCCAAAAATT | 54476 |
rs59695062 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF216 | GRCh38.p7 | 7:5726272 | CACAGGAGACCCTGT[C/G]TCAAACAAAACAAAA | 54476 |
rs59697888 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678883 | ACAAGCTGAGGAGGC[C/T]GAGCTCCTAGAGAGG | 54476 |
rs59728355 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RNF216 | GRCh38.p7 | 7:5691016 | CCACACACCCCCTGC[A/C]GCACCTTTTCTGCCT | 54476 |
rs59987579 | snp | C/T | 0.118933 | 0.212888 | intron-variant | RNF216 | GRCh38.p7 | 7:5634343 | CCAGGTCATGTGTGG[C/T]CACAGCTGTTGTTAA | 54476 |
rs60100761 | snp | A/C/G | 0.0178098 | 0.0926698 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5667707 | GGCAGGAACAGCCAG[A/C/G]AAAACCAGCTCCTGC | 54476 |
rs60181616 | snp | C/T | 0.110519 | 0.207473 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5670973 | AGTGTTTTCTGTGAA[C/T]TGCTTGGTTCCGGGG | 54476 |
rs60280795 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5716996 | ATAAATAAGGGAAAA[A/G]GCTGACACATAAAAC | 54476 |
rs60307322 | snp | A/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5687357 | GCTGAGACTGCGTCA[A/C]TGCTCCATCCTGGGC | 54476 |
rs60372872 | snp | A/T | 0.177824 | 0.239355 | intron-variant | RNF216 | GRCh38.p7 | 7:5750909 | ACTCAACAGAGAAGA[A/T]TCTGTGCAGTTGATG | 54476 |
rs60442234 | snp | A/G | 0.110167 | 0.207236 | intron-variant | RNF216 | GRCh38.p7 | 7:5732763 | GCAGTGGGGAAGCCT[A/G]TCGGACTTCAATCTG | 54476 |
rs60492601 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF216 | GRCh38.p7 | 7:5707577 | ATCTGTGAACTTGCA[C/T]GGATATAGATGCTTT | 54476 |
rs60889993 | snp | A/G | 0.118584 | 0.212673 | intron-variant | RNF216 | GRCh38.p7 | 7:5645681 | CTGCAACCTCCATCT[A/G]CCGGGTTCAAATGAT | 54476 |
rs60912551 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF216 | GRCh38.p7 | 7:5752584 | AATCCAACAGTAAGA[C/T]ACACTATAATGTTGT | 54476 |
rs61033429 | snp | A/C | 0.112631 | 0.208878 | intron-variant | RNF216 | GRCh38.p7 | 7:5706295 | ACATTTTTAAGTGTA[A/C]AGGGTCTGTTAGCAA | 54476 |
rs61043481 | in-del | -/A/AA/AG | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5765967 | AAAAAAAAAAAAAAA[-/A/AA/AG]GAAAGAAAGAAATAG | 54476 |
rs61163807 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF216 | GRCh38.p7 | 7:5695755 | GAGGGAAAAGCAAAA[A/C]CCCTGGTCAAACTGT | 54476 |
rs61203027 | snp | C/T | 0.330016 | 0.236849 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5667384 | TTCTTTAAAAAGGCA[C/T]CAAAAGGCTCATTCT | 54476 |
rs61210914 | snp | C/T | 0.168785 | 0.236441 | intron-variant | RNF216 | GRCh38.p7 | 7:5732502 | AATTCATTTTATATT[C/T]GCAACAATATTAAGA | 54476 |
rs61260366 | snp | C/T | 0.111224 | 0.207945 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5713481 | CTCTCCAGACCTTTC[C/T]TCCCCCTCAGTTTCA | 54476 |
rs61316901 | in-del | -/T | 0.333952 | 0.235483 | intron-variant | RNF216 | GRCh38.p7 | 7:5709746 | TGTGTGCCCTCAGGC[-/T]TTTATTTTTTAAATT | 54476 |
rs61336279 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF216 | GRCh38.p7 | 7:5739032 | CATATAGAAAGAAAG[G/T]AGGATGGTGGGTGCC | 54476 |
rs61344986 | snp | C/T | 0.298398 | 0.245271 | intron-variant | RNF216 | GRCh38.p7 | 7:5775152 | TGTTATTCACCATGG[C/T]CATAGAACCAGAGTC | 54476 |
rs61397031 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5633048 | GCAGTGGTGCGATCT[C/T]TGCTCACTGCAACCT | 54476 |
rs61405954 | snp | C/T | 0.410737 | 0.191478 | intron-variant | RNF216 | GRCh38.p7 | 7:5721923 | TCACTGATTTGGCAA[C/T]TTATGATTTTCTTTT | 54476 |
rs61753114 | snp | A/G | 0.0382633 | 0.132919 | synonymous-codon, utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5729519 | GAAGTCGGCCATGAG[A/G]AGGTCAGCAGCTTGG | 54476 |
rs61753532 | snp | C/T | 8.25403e-05 | 0.00642365 | missense, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5752947 | CTGAGGAGTCAGATA[C/T]GGTGATGGGCCCATC | 54476 |
rs61996492 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF216 | GRCh38.p7 | 7:5736513 | GGCCTCCCAAAGTGC[C/T]GAGATTTCAGCCTCT | 54476 |
rs61996493 | snp | C/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5736640 | AGGAAGTGAGGAGCG[C/T]CTCTTCCCGGCCGCC | 54476 |
rs62453427 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5629214 | AAAAAAAAAAAAAAG[A/T]GAAGACAATTCCAGT | 54476 |
rs62453428 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | RNF216 | GRCh38.p7 | 7:5641808 | GAGAGGCCAAAGCAG[A/G]AAGATCATTTGAGCT | 54476 |
rs62453429 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | RNF216 | GRCh38.p7 | 7:5648676 | GAGCTTGCAGTGAGC[C/T]GAGATAGCGCCACTG | 54476 |
rs62453430 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNF216 | GRCh38.p7 | 7:5648956 | GATATCAAAGACTTA[A/G]AATTTCAATTTTAGT | 54476 |
rs62453431 | snp | C/G | 0.5 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5676807 | AGCCACTGGACTCAG[C/G]TTCCAAGCACTTCCT | 54476 |
rs62453432 | snp | A/C | | | intron-variant | RNF216 | GRCh38.p7 | 7:5684445 | AGCCTCTGCATTAAA[A/C]CAAATGCTGATCTTT | 54476 |
rs62453448 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RNF216 | GRCh38.p7 | 7:5690232 | CTTGGGAGGCTGAGG[C/T]AGGAGAATCTCTTGC | 54476 |
rs62453450 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5726512 | GTGAGGATCCCTTTT[C/T]TTTCCTACCTTCAGC | 54476 |
rs62453452 | snp | C/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5736135 | CCTGTCCCTGTCCCT[C/G]TCCCTCTCCCCACAG | 54476 |
rs62455875 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5761801 | AAAAAAAAAAAAAAG[A/G]AATTATGTTTCAAAC | 54476 |
rs62455877 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768682 | TTTTTTTTTTTTTGG[G/T]ACAGAGTCTTGCTCT | 54476 |
rs62455878 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | RNF216 | GRCh38.p7 | 7:5769411 | GTGAGCCACCGCGCC[C/T]GGCCGCAAATGCCTT | 54476 |
rs62455879 | snp | G/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5772443 | TGTGCTTCTTGCTGT[G/T]TCACCCAGGCTGGAG | 54476 |
rs62455880 | snp | A/C | 0.39709 | 0.20215 | intron-variant | RNF216 | GRCh38.p7 | 7:5773681 | CAAGCGATTCTCCTG[A/C]CTCAGCCTCCCTGAG | 54476 |
rs62455881 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | RNF216 | GRCh38.p7 | 7:5776124 | TAGCTCTCCATATCC[A/G]TATGTGAAAGCTGTG | 54476 |
rs62455883 | snp | G/T | 0.421684 | 0.181726 | intron-variant | RNF216 | GRCh38.p7 | 7:5778814 | AGTGGCACAATCTCG[G/T]ATCACTGCAACCTCC | 54476 |
rs62455888 | snp | A/G | 0.454302 | 0.144085 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783649 | GGACAGAAAAAGACC[A/G]CTACTCATAGTGCTT | 54476 |
rs66511486 | in-del | -/A | 0.143284 | 0.226079 | intron-variant | RNF216 | GRCh38.p7 | 7:5697199 | CCCATCTCCGCCAAT[-/A]AGACCCCACCACGGC | 54476 |
rs66585249 | in-del | -/TT | 0.0248432 | 0.108648 | intron-variant | RNF216 | GRCh38.p7 | 7:5734373 | AGACTATACAAAATC[-/TT]TATGTAGTGTTCAAA | 54476 |
rs66617363 | in-del | -/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5660305 | TTTTTTTTTTTTTTT[-/G]GAGATGGAGTCTCGC | 54476 |
rs66824944 | in-del | -/A | 0.499035 | 0.0219437 | intron-variant | RNF216 | GRCh38.p7 | 7:5774728 | ACAGTTCAAGGGGGG[-/A]AAAAAATCTTTATTT | 54476 |
rs67935203 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5774192 | TAAATCTTGGTTTCC[-/A]CATTTAGTCAATCGG | 54476 |
rs68129648 | in-del | -/T | 0.47852 | 0.101384 | intron-variant | RNF216 | GRCh38.p7 | 7:5769122 | ACAGTTCCAAATGCC[-/T]TTTTTTTTTTTTTTT | 54476 |
rs71004690 | in-del | -/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5621190 | TTTTTTTTTTTTTTT[-/T]AAAGATAGAGTTTTG | 54476 |
rs71004692 | in-del | -/AAACA | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5705964 | AAACAAAACAAAACA[-/AAACA]CCACTCTGGGAGGCC | 54476 |
rs71004693 | in-del | -/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5714816 | GATGATGAACGAAGG[-/G]AGGTGCTCCTCTGCG | 54476 |
rs71004694 | in-del | -/TAAATAAATAAA | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5734868 | AAATAAATAAATAAA[-/TAAATAAATAAA]AGGTTTGCAGGGCAT | 54476 |
rs71004695 | in-del | -/GTCCCT | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5736135 | CCTGTCCCTGTCCCT[-/GTCCCT]CTCCCCACGGTCTCC | 54476 |
rs71004696 | in-del | -/AA | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5738731 | AAAAAAAAAAAAAAA[-/AA]TGCTTCCATGTATTT | 54476 |
rs71004697 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5740002 | GTCTCAAAAAAAAAA[-/A]CAAACCAAAAACAAA | 54476 |
rs71004698 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTT | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5740119 | CTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTTT]GTGAGATAGAGTCTC | 54476 |
rs71004699 | in-del | -/CACACACA | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5748651 | ACACACACACACACA[-/CACACACA]TAATATACTAACTAA | 54476 |
rs71004700 | in-del | -/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5749150 | AAAAATGCCCATGTA[-/T]TTTTTTTTTTTTTTT | 54476 |
rs71004701 | in-del | -/AAAAA | 0.494896 | 0.0502606 | intron-variant | RNF216 | GRCh38.p7 | 7:5765788 | CAAAAAAAAAAAAAA[-/AAAAA]TTAGCCAGGCGTGGC | 54476 |
rs71004702 | in-del | -/CACACA | 0 | 0 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768393 | ACACACACACACACA[-/CACACA]GCTTAAATTGACAGA | 54476 |
rs71524560 | multinucleotide-polymorphism | AA/GC | 0 | 0 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783420 | CAGGAGCGAGCCACT[AA/GC]ACCCGGCCAGAGGAT | 54476 |
rs71531329 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF216 | GRCh38.p7 | 7:5638556 | CAGCCAGGTACTATT[C/T]TCATTTCCATTTATT | 54476 |
rs71531330 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF216 | GRCh38.p7 | 7:5697310 | ATGGTCAGTTAGGGC[C/T]GTGGTTGCCCTTTCT | 54476 |
rs71531331 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5702292 | CGGGCCAAGGGGAGA[A/G]GCAGGTGCTTCTACC | 54476 |
rs71531332 | snp | C/T | 0.00562761 | 0.052746 | intron-variant | RNF216 | GRCh38.p7 | 7:5730837 | AGAAACAAATGATGT[C/T]ACTTTCATACTGCTT | 54476 |
rs71547783 | in-del | -/A | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5626670 | AGTGAAACTTGTGTT[-/A]AAAAAAAAAAAAAAG | 54476 |
rs71547784 | in-del | -/A/AA | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5629826 | GCAAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 54476 |
rs71547785 | in-del | -/A | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5653601 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54476 |
rs71547786 | in-del | -/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5660264 | GGCCCTGTTTTAAAT[-/T]CTTTTTTTTTTTTTT | 54476 |
rs71547787 | in-del | -/ACACACAC | | | intron-variant | RNF216 | GRCh38.p7 | 7:5748612 | ATTTTTTATATACAT[-/ACACACAC]ACACACACACACACA | 54476 |
rs71547789 | in-del | -/AC/ACAC | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768346 | CCGAGGCAGGCAAAT[-/AC/ACAC]ACACACACACACACA | 54476 |
rs71547791 | in-del | -/A | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5779828 | GCCAGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA | 54476 |
rs71941013 | in-del | -/T | 0.493748 | 0.0555599 | intron-variant | RNF216 | GRCh38.p7 | 7:5638633 | GTAGAAAAGCAAGCA[-/T]TTTTTTTTTTTTTTT | 54476 |
rs71971690 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5686225 | TATGACTCTGTTATT[-/A]AAAAAAAAAAAAAAA | 54476 |
rs72196246 | in-del | -/CT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5632987 | CTGGAAGAGCACTTT[-/CT]GTTTTTTTTGAGACA | 54476 |
rs72421808 | in-del | -/A | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5689371 | CATATTTGTAGTATT[-/A]AAAAAAAAAAAAAAA | 54476 |
rs72484515 | in-del | -/GT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5757416 | TCAGCTCTTTTTGTG[-/GT]TGTGTGTGTGGCTAT | 54476 |
rs72564339 | in-del | -/C/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5715608 | GGAGTGCGAATGGGT[-/C/G]STATCGAGGTCTGCG | 54476 |
rs72564340 | in-del | -/TC | 0.32955 | 0.237006 | intron-variant | RNF216 | GRCh38.p7 | 7:5755979 | ATACTGTCTATAGAT[-/TC]TGATATGGTTTGGCT | 54476 |
rs73048704 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5753145 | AGAGCCATGTTTCTA[A/T]GCTGACTTTTGCCAA | 54476 |
rs73048722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5765372 | GGGAGGCTGAGGTAA[A/G]AGAATTGCTTCAGCT | 54476 |
rs73048736 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF216 | GRCh38.p7 | 7:5779960 | TCCCCCACCTACATC[C/T]CATTCAGTAAACAAA | 54476 |
rs73052800 | snp | C/T | | | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5622244 | GCAACAGAACAAAAC[C/T]CCCGCCGCGAGATGG | 54476 |
rs73054731 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5674726 | ATAGTTGTGCAAAGC[A/G]GGGGGTCTTTAAAGC | 54476 |
rs73062695 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677016 | ACCAACCACATGAAA[C/T]GAACCTCGTAAGAGA | 54476 |
rs73062697 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679182 | GAGGATCCTGTCACC[C/T]TCGGGTAGGGGTGGT | 54476 |
rs73062700 | snp | A/G | | | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679846 | TATCATGCTCCTCCA[A/G]GTCCCTCACCCGCCT | 54476 |
rs73064604 | snp | C/T | 0.203267 | 0.245593 | intron-variant | RNF216 | GRCh38.p7 | 7:5685557 | AGGCAAATTCTATTA[C/T]TTTTTCCTCTTTCCT | 54476 |
rs73064610 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RNF216 | GRCh38.p7 | 7:5701256 | ATCTACCCCTTTACA[C/T]GGCAGAACACTGGGG | 54476 |
rs73064612 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | RNF216 | GRCh38.p7 | 7:5709090 | ATGCTGGACTCATGC[G/T]CCAACTCCTTCCCTC | 54476 |
rs73064615 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5709946 | TTTTTTTTGTAGAGA[G/T]AGGGTCTATGTTGCT | 54476 |
rs73064628 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF216 | GRCh38.p7 | 7:5715702 | ATTGACTCCTTTTAT[C/T]AACTATAGCAACGGA | 54476 |
rs73064636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF216 | GRCh38.p7 | 7:5721527 | CGCTGCTTATAGCCA[C/T]TTGTTGGTGAATGTA | 54476 |
rs73064643 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5731014 | TATCTTTGTGAAAGA[C/T]AAAAAAATTTAAAAA | 54476 |
rs73064649 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF216 | GRCh38.p7 | 7:5735386 | ATGATTCCCAAGAAC[G/T]TAACATATCAGAACA | 54476 |
rs73064662 | snp | C/G | 0.408371 | 0.212078 | intron-variant | RNF216 | GRCh38.p7 | 7:5748531 | ATAGGCGTGAGCCAC[C/G]GTGTCCAGTTTCTTT | 54476 |
rs73336224 | snp | C/T | 0.0329836 | 0.124112 | downstream-variant-500B, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5619686 | GAACCTTGTCCCCTC[C/T]TCAGCTGGGCGAGGC | 54476 |
rs73336227 | snp | C/T | 0.0329836 | 0.124112 | downstream-variant-500B, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5619846 | TGGTAGCCGCCCTAG[C/T]GGGATTTGCCTAGCA | 54476 |
rs73336234 | snp | C/G | 0.0433465 | 0.140692 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621334 | CATGCGCCACCTTGT[C/G]CGGCTAATTTTGTAT | 54476 |
rs73336241 | snp | A/G | 0.0329836 | 0.124112 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621498 | AAATACATCTGAGAA[A/G]CCAATGGCAGCGAAT | 54476 |
rs73338039 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF216 | GRCh38.p7 | 7:5638788 | GACTACAGGTGAGCA[C/T]CACATCTGGCTAATT | 54476 |
rs73338056 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | RNF216 | GRCh38.p7 | 7:5646207 | AGTGACTTTTAAAAA[G/T]TATTTTTGTAAATTA | 54476 |
rs73338057 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | RNF216 | GRCh38.p7 | 7:5646802 | GGAAAAAAAAAAAAT[C/G]AAAGAACCAATCCTC | 54476 |
rs73338062 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | RNF216 | GRCh38.p7 | 7:5650369 | AACCAGTGCCAGGAA[A/C]CGATAGGACAATCAG | 54476 |
rs73338063 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF216 | GRCh38.p7 | 7:5650903 | GGGAAACTGCCCAAA[C/T]TGCCATTGCCCACTT | 54476 |
rs73338064 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | RNF216 | GRCh38.p7 | 7:5651080 | TAATTCCTGTATCAC[G/T]TATAACATAAAGAAA | 54476 |
rs73338065 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF216 | GRCh38.p7 | 7:5651527 | CTGAGCTACCCTGCC[C/T]GGCTGTGAGACAATC | 54476 |
rs73338067 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | RNF216 | GRCh38.p7 | 7:5652275 | GAGGCTCAAGGGTTA[C/G]ATTACTTCCCCAAGA | 54476 |
rs73338074 | snp | C/T | 0.178785 | 0.239642 | intron-variant | RNF216 | GRCh38.p7 | 7:5659243 | ATTTGTATGAGACAC[C/T]GGAGATACAGCAATA | 54476 |
rs73338077 | snp | G/T | 0.134119 | 0.221521 | intron-variant | RNF216 | GRCh38.p7 | 7:5659866 | CTGTACTTTTTTTGT[G/T]AAGAAGAAGAGAACC | 54476 |
rs73338091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5663230 | TGCGGCAAAGATGAC[A/G]TCCTGCTGGTCACTA | 54476 |
rs73338095 | snp | A/G | 0.130351 | 0.219509 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5664074 | CTAGGGCCTAGCACT[A/G]GATTTGAGCGGCACA | 54476 |
rs73338096 | snp | A/G | 0.124144 | 0.21601 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5666768 | TTGCTCCCCATAGAT[A/G]CTCCATACAATACAG | 54476 |
rs73339903 | snp | C/T | 0.127944 | 0.218179 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5669480 | AAGTGAAAGATTATA[C/T]TGACAGATTTAGCAG | 54476 |
rs73339924 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678973 | TAGAAATGGCCTCAA[C/T]AGAGCAAAGAGGAAA | 54476 |
rs73339926 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679436 | ATGCAGGCGCTGAGC[A/G]CACTGGTGCACACAC | 54476 |
rs73339928 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679845 | CTATCATGCTCCTCC[A/C]GGTCCCTCACCCGCC | 54476 |
rs73339931 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5681340 | TTTTAGGAAAAAATA[C/T]AAACTTTATTCTGAA | 54476 |
rs73339935 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5681552 | ACCTGTAGCACCAAG[G/T]ACAGTGTCTTCCTCC | 54476 |
rs73339936 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5681743 | AAACCACACTGCTCA[C/G]CTTCAACACTCCGGC | 54476 |
rs73339944 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5684737 | GTGTTCAAGCAATGT[C/G]TTCTTCAAGGCACCT | 54476 |
rs73339951 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5686714 | ATGACATATTACCTA[C/G]AGAAGATCTTAAAAC | 54476 |
rs73339962 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5688839 | CTTAATAATATGATA[C/T]GAATTCCCAAATGAT | 54476 |
rs73339967 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5694808 | ACAGCCACTCTCTCA[A/G]AGTGTTCTAGGTGTT | 54476 |
rs73339969 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF216 | GRCh38.p7 | 7:5695239 | TACAACTGCAAGTCA[A/G]GAGTACCAAATACCA | 54476 |
rs73339973 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | RNF216 | GRCh38.p7 | 7:5697218 | CCCCACCACGGCCTG[C/G]TCAGGCCCAGACCCA | 54476 |
rs73339992 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5714085 | TCAGCTCACTAAGCC[A/T]CCCGAGTAGCTGGAT | 54476 |
rs73341604 | snp | C/T | 0.135825 | 0.222405 | intron-variant | RNF216 | GRCh38.p7 | 7:5719936 | GAAGACTTCATTTTA[C/T]TACACAGAATATTGA | 54476 |
rs73341611 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | RNF216 | GRCh38.p7 | 7:5720614 | TAGTTATAAGAGGTT[A/T]GACCTCGCAGACCCC | 54476 |
rs73341614 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RNF216 | GRCh38.p7 | 7:5721681 | TGAGTTCCAGTCTCT[C/G]CATGTCCTTACCAAC | 54476 |
rs73341621 | snp | A/G | 0.140242 | 0.224618 | intron-variant | RNF216 | GRCh38.p7 | 7:5722939 | TGGGAAGTGGACTCC[A/G]TCTTAAAATTAAAAA | 54476 |
rs73341623 | snp | A/T | 0.122411 | 0.214991 | intron-variant | RNF216 | GRCh38.p7 | 7:5722992 | CAGTTTTTGGTATTA[A/T]GAGAATAGAAAAGCA | 54476 |
rs73341624 | snp | C/T | 0.138546 | 0.223781 | intron-variant | RNF216 | GRCh38.p7 | 7:5723288 | TTTCTTTCGTCTTTA[C/T]TCAGTTCTTTTTGTA | 54476 |
rs73341641 | snp | C/T | 0.116838 | 0.211584 | intron-variant | RNF216 | GRCh38.p7 | 7:5730929 | CACATTACAACTGGC[C/T]TATCAAGAAATTAAG | 54476 |
rs73341665 | snp | A/G | 0.118235 | 0.212457 | intron-variant | RNF216 | GRCh38.p7 | 7:5746811 | ATTCAGAATTATGAT[A/G]ACCATGATGTGGAAT | 54476 |
rs73341666 | snp | C/G | 0.130351 | 0.219509 | intron-variant | RNF216 | GRCh38.p7 | 7:5747376 | TAAAAACGGATAAAA[C/G]CAGCAGAAGCAGAAT | 54476 |
rs73341668 | snp | A/G | 0.131381 | 0.220067 | intron-variant | RNF216 | GRCh38.p7 | 7:5747614 | ACAAAGGTCATGCAC[A/G]GTGGCACACACCTGT | 54476 |
rs73343307 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | RNF216 | GRCh38.p7 | 7:5769069 | AAATATATCAAAATT[A/T]ATGTGAAGGAGGTAA | 54476 |
rs73343309 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF216 | GRCh38.p7 | 7:5771716 | GTGGGAAGATCTCTT[A/G]AGCTCGAGAGGTGGA | 54476 |
rs73343321 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF216 | GRCh38.p7 | 7:5777132 | CCAGTGGAGCCCGGC[C/T]TTCCAGCAGTCTTTG | 54476 |
rs73673146 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678477 | CATGCCACCTGGCGT[C/T]CCCACATGACCTGGT | 54476 |
rs73673148 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNF216 | GRCh38.p7 | 7:5685324 | TTCCATGAATAAAAC[A/G]TGATTAATGTCAGGA | 54476 |
rs73673151 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RNF216 | GRCh38.p7 | 7:5687811 | TAAGAGTTTTGCAAA[C/T]ATCCCCTCCTTTAAT | 54476 |
rs73673173 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF216 | GRCh38.p7 | 7:5696986 | TCCATTACGCCAGCA[A/G]CAGCTCCAGGGACGG | 54476 |
rs73673177 | snp | A/G | 0.151001 | 0.229563 | intron-variant | RNF216 | GRCh38.p7 | 7:5710460 | AGCACTTTCACTGGC[A/G]GACCTTCTTTGAAAC | 54476 |
rs73673188 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RNF216 | GRCh38.p7 | 7:5730176 | ATGCTGAAGTACTTA[C/G]AGGGAAGTGTACTCA | 54476 |
rs73673190 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RNF216 | GRCh38.p7 | 7:5734545 | AAAACTATACACAAT[A/G]AAGAATATGTGGAAA | 54476 |
rs73673519 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | RNF216 | GRCh38.p7 | 7:5778595 | AGATGATCTTCAATA[C/G]TAGATGTACTTTCAG | 54476 |
rs73676614 | snp | A/G | 0.0236746 | 0.106192 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5621517 | ATGGCAGCGAATGAC[A/G]GTGCCCGCCTGCCCC | 54476 |
rs73676615 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF216 | GRCh38.p7 | 7:5625357 | TAATGAAAGCACATT[C/T]ATTTTCCTAGACACG | 54476 |
rs73676616 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF216 | GRCh38.p7 | 7:5628353 | AATCATGAGCCAACT[A/G]TCAGTTATACCTAGA | 54476 |
rs73676618 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF216 | GRCh38.p7 | 7:5632428 | CAGCTCCTTTCTGAT[A/G]AGCAAGGCCAGGCTG | 54476 |
rs73676621 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF216 | GRCh38.p7 | 7:5635808 | TTAACATCTATAAAT[A/G]TTAGGCTCAGTCCAC | 54476 |
rs73676627 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | RNF216 | GRCh38.p7 | 7:5649667 | GGCATCTTCTAGACT[C/G]GCACCACCATCAAAG | 54476 |
rs73676628 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF216 | GRCh38.p7 | 7:5650947 | CCAAACTCCTTCCAT[A/G]TCCTTCATATTTAAA | 54476 |
rs74302786 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5691611 | AATGCCCAGCTTCTC[C/T]TTAGGGGCAACATGT | 54476 |
rs74339427 | snp | A/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5774728 | TACAGTTCAAGGGGG[A/G]AAAAAATCTTTATTT | 54476 |
rs74349839 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673146 | CTCTACAACACCAAA[C/T]GCCCCACCTGCGGGC | 54476 |
rs74392896 | snp | G/T | 0.120326 | 0.21374 | intron-variant | RNF216 | GRCh38.p7 | 7:5653191 | CCTTAAAAGTTTCAC[G/T]TCATATATAAACATG | 54476 |
rs74433509 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5665640 | ATAGCTGCCGGCTTT[C/T]TACTATACTATGGGG | 54476 |
rs74454750 | snp | C/T | 0.178465 | 0.239547 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783699 | GGAATAGTCATGTTT[C/T]AGTGAAGTAGAAATT | 54476 |
rs74457480 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF216 | GRCh38.p7 | 7:5694683 | GCCCTGGAGCAGAGA[C/T]GTGTATGGTGGCCAT | 54476 |
rs74510355 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | RNF216 | GRCh38.p7 | 7:5625206 | CAAGCAGGAAAGAGA[G/T]AGCTGACTATAGGAG | 54476 |
rs74511814 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF216 | GRCh38.p7 | 7:5644017 | GTTGTAGCATGTATC[A/G]ATACTTCATTCCTTT | 54476 |
rs74523492 | snp | A/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5626684 | TTAAAAAAAAAAAAA[A/G]GGAAGAAAGAAAAAA | 54476 |
rs74536515 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF216 | GRCh38.p7 | 7:5738836 | CACAGGTAGTATCAA[C/T]GCTTAGAAACAACTC | 54476 |
rs74557531 | in-del | -/A | | | intron-variant | RNF216 | GRCh38.p7 | 7:5727942 | AGGATTTTTTTTTTA[-/A]TYCTCCTTGGGTTTT | 54476 |
rs74560032 | snp | C/G | | | intron-variant | RNF216 | GRCh38.p7 | 7:5778285 | CAGGCTCTTCCCCAG[C/G]TAAACTACTCTTCTT | 54476 |
rs74567147 | snp | C/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5770802 | AGTGCAGAACAGATT[C/T]TTTTTTTTTTTTTCT | 54476 |
rs74570281 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF216 | GRCh38.p7 | 7:5759213 | TCCTAAGGCCTCCCC[A/C]AGAAGCAGAGGCCGC | 54476 |
rs74572899 | snp | C/G | 0.0711525 | 0.174681 | intron-variant | RNF216 | GRCh38.p7 | 7:5696999 | CAACAGCTCCAGGGA[C/G]GGGGGTAGGGGAAGT | 54476 |
rs74601119 | snp | C/T | 0.11963 | 0.213316 | intron-variant | RNF216 | GRCh38.p7 | 7:5631499 | CTGTTCTCAGCTCAC[C/T]GGTTTTGGTCCATCT | 54476 |
rs74609589 | snp | A/C | 0 | 0 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5782848 | GTGAGACTGTGTCTC[A/C]AAAAAAAAAAAATTG | 54476 |
rs74623215 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | RNF216 | GRCh38.p7 | 7:5640256 | GTCATTTGCCAGTGA[A/G]AATTTATTATTTTTT | 54476 |
rs74635373 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RNF216 | GRCh38.p7 | 7:5651577 | TAGATATGCACCCTC[A/G]GCTGCATGGTAAGGC | 54476 |
rs74664421 | snp | C/T | 0.116488 | 0.211364 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5663229 | TTGCGGCAAAGATGA[C/T]GTCCTGCTGGTCACT | 54476 |
rs74664919 | snp | G/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5644524 | CCATTTTTTTTTTTT[G/T]AGACAGAGTCTCACT | 54476 |
rs74667690 | snp | A/G | 0.5 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679725 | CAATTAAACAAAAAA[A/G]GAAAGGCAGGCACCA | 54476 |
rs74670490 | snp | A/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5774770 | GTTACTTTTTTTTTT[A/T]TTATTGAGACGAAGT | 54476 |
rs74694240 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF216 | GRCh38.p7 | 7:5639222 | CAGCCCCTTTGCTGC[C/T]TGGAATGTGGATTTA | 54476 |
rs74697371 | snp | C/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5714267 | CGCCTGGCCTATTTT[C/T]CTTTTTTAGAGATGG | 54476 |
rs74727296 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | RNF216 | GRCh38.p7 | 7:5701233 | TAGCAAAAAAATCAG[A/G]TTGAAAAATCTACCC | 54476 |
rs74729615 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF216 | GRCh38.p7 | 7:5660665 | TCACTGCAGTCGCGA[A/C]CTCCCTGGCTCAAGC | 54476 |
rs74730335 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF216 | GRCh38.p7 | 7:5691434 | AGGAACAGATGAATG[C/T]GTAAGTGTACAAGAG | 54476 |
rs74735036 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF216 | GRCh38.p7 | 7:5763002 | TCCATGGACCAGCAA[C/T]GGAACAGAAACACAG | 54476 |
rs74780509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5706728 | CAATTCCTTTCCACC[A/G]GCTGCCTTTTCACTC | 54476 |
rs74807136 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5682598 | TTTTAGTAGAGACGG[A/G]GTTTCTCCATCTTGG | 54476 |
rs74822584 | in-del | -/AAT | | | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754333 | GTTACTTAAAAAAAA[-/AAT]TTTTTTTTGTAGAGA | 54476 |
rs74866077 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RNF216 | GRCh38.p7 | 7:5766215 | GGATCTCCTGAACCC[A/G]GGAGTTTGATGTTGC | 54476 |
rs74873233 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5670265 | AAACAACCTGGATGT[C/G]AGACTTTCAGGATCC | 54476 |
rs74888230 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | RNF216 | GRCh38.p7 | 7:5625984 | TCTGTTTTCAGCAAA[A/G]GGAGCCTCCTTGCTG | 54476 |
rs74932671 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5740907 | TTTTTTTTTGCAATG[A/G]AAAAAAAAAAAGAAA | 54476 |
rs74981409 | snp | A/C | 0.0887219 | 0.191022 | intron-variant | RNF216 | GRCh38.p7 | 7:5766361 | CTCTAAAGTGTGTCA[A/C]GCCTGGCCTCCAAAT | 54476 |
rs75029104 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5696425 | CATGGTTTCCTCCTT[A/T]TGTAAAGCACCTGAG | 54476 |
rs75044963 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF216 | GRCh38.p7 | 7:5763622 | GTCATCCTGGCTGGA[A/G]AGCAGCTACACGATC | 54476 |
rs75048246 | snp | C/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5769123 | CAGTTCCAAATGCCT[C/T]TTTTTTTTTTTTTTT | 54476 |
rs75064103 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | RNF216 | GRCh38.p7 | 7:5755942 | ACGTCCTTATGGGAA[A/C/T]ACAATCATGCTCATT | 54476 |
rs75064653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5692674 | CCGAGGCAAGGCACT[C/G]CTTTTTAGGTGGTAA | 54476 |
rs75070395 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF216 | GRCh38.p7 | 7:5650106 | GTGTCATCTCTATGA[A/G]GTTCTGGTGGTCTGG | 54476 |
rs75073149 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5751640 | TTATTTTTCTCTTTT[C/T]TGTCTCCCTGTCCCA | 54476 |
rs75077694 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RNF216 | GRCh38.p7 | 7:5627995 | ACCTGCATAGGAGCG[C/T]GAGCCCAGGTTTCTG | 54476 |
rs75078175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5720633 | CTCGCAGACCCCCAA[G/T]AGAGTCTTGGGAAAC | 54476 |
rs75105904 | snp | A/T | 0 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673859 | CTCTCTCTTTCTCTC[A/T]TTTTTTTTTTTTTTT | 54476 |
rs75120026 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677747 | CCTGGGAGTGTTGCT[C/T]AGGAAATCCTAGGAA | 54476 |
rs75148631 | snp | A/G | 0.00978625 | 0.0692629 | synonymous-codon, utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5741201 | CGGCCTTGGAAAAGC[A/G]GGCCCTGGGAATTCA | 54476 |
rs75165128 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF216 | GRCh38.p7 | 7:5715550 | GGAGTATGAGAGATG[C/T]TACCCAAAAAACTTT | 54476 |
rs75168566 | snp | C/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5724782 | TTTACTGGGTGGAAG[C/T]AACTCAGATAAAATC | 54476 |
rs75175715 | in-del | -/AAA | | | intron-variant | RNF216 | GRCh38.p7 | 7:5733677 | CCAAAAAAAAAAAAA[-/AAA]GGAATTCAAAGAGAA | 54476 |
rs75177193 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | RNF216 | GRCh38.p7 | 7:5631800 | CCTGGGAACATTCTG[A/C]TATCTTTTCCATTGG | 54476 |
rs75218133 | snp | C/G | 0.046775 | 0.145601 | intron-variant | RNF216 | GRCh38.p7 | 7:5643544 | GTTATCTGTGCTCAC[C/G]ACCAGCCAGTGTGTG | 54476 |
rs75284702 | snp | A/G | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5744980 | CCCATCTCCAAAAAG[A/G]AAAAAAAAAAAGAAA | 54476 |
rs75307927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5764895 | AAACTTGGTGAGACC[C/T]CATCTCTACAAAAAA | 54476 |
rs75320413 | snp | A/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5771173 | TGGAAAACATGACCT[A/T]TCTACTATATGATGC | 54476 |
rs75365330 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5682103 | CACTCAGCAGACACA[A/G]GCACCTGAGGCCATG | 54476 |
rs75365889 | snp | A/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5742458 | GTTCAAAAAACATAT[A/T]AAAAAATCTAAATCT | 54476 |
rs75396364 | snp | A/C | 0.118933 | 0.212888 | intron-variant | RNF216 | GRCh38.p7 | 7:5653129 | CACCAGGGGCTCCTA[A/C]GGGAGACTTTCCTCC | 54476 |
rs75414874 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | RNF216 | GRCh38.p7 | 7:5755201 | AAGGAAGGAAGGAAG[A/G]GAGGGAAGGAAGAAA | 54476 |
rs75422147 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | RNF216 | GRCh38.p7 | 7:5739160 | TGCATAATAATGTGA[A/C]TTTACTTAACAACAC | 54476 |
rs75445286 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF216 | GRCh38.p7 | 7:5638676 | AGGGTCTTGCTCTGT[C/T]ACCCAGGCTACAGTG | 54476 |
rs75450619 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | RNF216 | GRCh38.p7 | 7:5623713 | AGCTGGGATCGCAGA[C/T]GTGTGCCAACACACC | 54476 |
rs75454051 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF216 | GRCh38.p7 | 7:5645008 | TTTTGCATTTTTAGG[C/T]GTTTCATCATATTGG | 54476 |
rs75505177 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RNF216 | GRCh38.p7 | 7:5695280 | CCACCTGCGCAGACC[A/C]AGTGCAGCAACTTGT | 54476 |
rs75510328 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | RNF216 | GRCh38.p7 | 7:5625610 | TGAGTGATTTCCCCA[C/T]ACAATTGTTTGTGAA | 54476 |
rs75515388 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | RNF216 | GRCh38.p7 | 7:5646151 | TTATACTGAGAAGAG[G/T]CTAGAAATCAGGTTG | 54476 |
rs75525475 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF216 | GRCh38.p7 | 7:5736717 | CGGTGGGGCAGAGGC[G/T]CTCCCCACATCTCAG | 54476 |
rs75559821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF216 | GRCh38.p7 | 7:5659415 | GAGGGAAGAGCAAGG[A/G]TGAAGGCTTCAGGGC | 54476 |
rs75569213 | snp | A/C | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5742447 | GAATAAGAAATGTTC[A/C]AAAAACATATAAAAA | 54476 |
rs75607331 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF216 | GRCh38.p7 | 7:5740002 | AGTGAGACTCGGTCT[A/C]AAAAAAAAAACAAAC | 54476 |
rs75610991 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | RNF216 | GRCh38.p7 | 7:5630895 | TGACCCAGGCAATCT[C/T]GTCTCAAAGCCTGAG | 54476 |
rs75618025 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | RNF216 | GRCh38.p7 | 7:5755434 | AATTAATACAAAGGG[C/T]CATCTGTGTATAATC | 54476 |
rs75644820 | snp | C/T | 0.0108441 | 0.0728318 | intron-variant | RNF216 | GRCh38.p7 | 7:5752799 | GGCTGAAAAATCAGA[C/T]CACCAACTTGCAATA | 54476 |
rs75658756 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5711976 | CTCCTTAGTTTTCCT[C/T]AAAAACACAGATTGA | 54476 |
rs75713038 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RNF216 | GRCh38.p7 | 7:5746248 | TGAGAGAGCATTTGA[C/T]TTTGCAGTACCTAGG | 54476 |
rs75723744 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680812 | ACACAGCCACCCACT[C/G]GCTGCTCATGCAACA | 54476 |
rs75742717 | snp | G/T | 0.427119 | 0.176434 | intron-variant, utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5780280 | GACCTGGCCAGGCTG[G/T]AGCCAGGTGCATGTG | 54476 |
rs75802369 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF216 | GRCh38.p7 | 7:5643506 | CCTCTTCTATGCAGC[C/T]AGCGACAGCCCAGAC | 54476 |
rs75840695 | snp | C/G | 0.105924 | 0.204309 | intron-variant | RNF216 | GRCh38.p7 | 7:5748716 | AGTATGCTATTAGTA[C/G]TTAAGTAGTTATTAA | 54476 |
rs75881621 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF216 | GRCh38.p7 | 7:5635588 | GCCGCTTAAGCCAGG[G/T]TCCCAAAGGTCCCCA | 54476 |
rs75922671 | snp | C/T | 0.0509478 | 0.151255 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768077 | GTACTCTAATTTGCA[C/T]ACCTAAAAAACTTAA | 54476 |
rs75923427 | snp | C/G | 0.106278 | 0.204558 | intron-variant | RNF216 | GRCh38.p7 | 7:5747497 | CTTAGAAAGCCATTT[C/G]CAAAATGTTTCAGCT | 54476 |
rs75926517 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768168 | TGATTAAAAAAAAAA[C/T]TACCAGGTGCGGTAG | 54476 |
rs75943063 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | RNF216 | GRCh38.p7 | 7:5633794 | GATGGCAAGCACCCG[A/G]CCTTTCCAGAAACGT | 54476 |
rs75944082 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677524 | ATATGGCTTCTGGTA[A/G]ATTATAATAATGGCA | 54476 |
rs75954616 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5621110 | CCTTACCCCAGGTCC[A/G]GGTGACCACCTGTCT | 54476 |
rs75988812 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768309 | GAAAAAAAAAAAAAA[A/G]GGCTGGGTCCAGTAG | 54476 |
rs75999980 | snp | C/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5709746 | TGTGTGCCCTCAGGC[C/T]TTTATTTTTTAAATT | 54476 |
rs76010341 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5783300 | ACGCCCGGCTAATTT[A/T]CGTATTTTCAGTAGA | 54476 |
rs76019383 | snp | C/T | 0.111224 | 0.207945 | intron-variant | RNF216 | GRCh38.p7 | 7:5763242 | CACTCCACATATTGA[C/T]TGTGGTGGTAGTCAC | 54476 |
rs76032496 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | RNF216 | GRCh38.p7 | 7:5740117 | ACCTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTTTTT]GTGAGATAGAGTCTC | 54476 |
rs76094431 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | RNF216 | GRCh38.p7 | 7:5766530 | TTGCTTTTTCTCTCC[A/G]TCATGTGAGAACACA | 54476 |
rs76104298 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5761799 | ACAAAAAAAAAAAAA[A/G]GGAATTATGTTTCAA | 54476 |
rs76162924 | snp | A/C | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5742446 | AGAATAAGAAATGTT[A/C]AAAAAACATATAAAA | 54476 |
rs76196077 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF216 | GRCh38.p7 | 7:5648916 | CTAATTTGAGATAAT[C/T]AGTGGAACTGTGAAG | 54476 |
rs76226526 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF216 | GRCh38.p7 | 7:5698322 | ACACAGAACCCCAGG[C/G]TTCCTGGGAACCCAA | 54476 |
rs76267851 | snp | A/C | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5714806 | AATACAAATAAGATG[A/C]TGAACGAAGGAGGTG | 54476 |
rs76334859 | snp | A/C | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5765952 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 54476 |
rs76343407 | snp | C/T | 0.167484 | 0.23599 | intron-variant, utr-variant-5-prime | RNF216 | GRCh38.p7 | 7:5777555 | ATCTGTGTATGTCAC[C/T]GGCCATCAGGGCAAG | 54476 |
rs76362175 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | RNF216 | GRCh38.p7 | 7:5688063 | GACCGCAAATGGAAC[C/T]GAAGAGGTAATTAGA | 54476 |
rs76368066 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF216 | GRCh38.p7 | 7:5658861 | TCTGATACGGCAAGC[A/G]ATAAAATTGTACATC | 54476 |
rs76385326 | in-del | -/A | 0.230896 | 0.249269 | intron-variant | RNF216 | GRCh38.p7 | 7:5776421 | ACCCCGTCTCTACTT[-/A]AAAAAAAAAAAAAGC | 54476 |
rs76401198 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | RNF216 | GRCh38.p7 | 7:5622345 | GCACGGGTTTTGGAT[G/T]GGGGGACAGCATCTT | 54476 |
rs76406015 | snp | G/T | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5742608 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGACAGAGT | 54476 |
rs76428382 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RNF216 | GRCh38.p7 | 7:5708783 | AGGCATCTAGAGTAG[A/G]TTGGGTTCTGCCAGC | 54476 |
rs76472186 | snp | A/G | 0.170733 | 0.237101 | intron-variant | RNF216 | GRCh38.p7 | 7:5759227 | CCAGAAGCAGAGGCC[A/G]CTATGTTTCCTATAC | 54476 |
rs76505470 | snp | A/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5625359 | ATGAAAGCACATTTA[A/T]TTTCCTAGACACGGC | 54476 |
rs76506063 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5626686 | AAAAAAAAAAAAAAG[A/G]AAGAAAGAAAAAAGA | 54476 |
rs76510211 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF216 | GRCh38.p7 | 7:5651595 | TGCATGGTAAGGCTA[C/G]ATTGTTATGAGAGAA | 54476 |
rs76528899 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF216 | GRCh38.p7 | 7:5775274 | GAAGAAAAGAGAATC[A/G]CTCACGGTTCTCTCA | 54476 |
rs76535405 | snp | A/G | 0.175254 | 0.238565 | intron-variant | RNF216 | GRCh38.p7 | 7:5659933 | ACTATTCTTCTTAAT[A/G]TTTTAATTACATTCA | 54476 |
rs76558338 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF216 | GRCh38.p7 | 7:5637670 | CCCTGGAAGGAGCTG[A/G]GAACACAGGTGTGCA | 54476 |
rs76565596 | snp | A/G | 0.084364 | 0.187256 | intron-variant | RNF216 | GRCh38.p7 | 7:5648846 | CAATTATCAAATGCA[A/G]TGAATCTCATTTGGA | 54476 |
rs76565957 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5703617 | CAGAAAAACAAGCAG[G/T]GAAGAAAGCTGGCAG | 54476 |
rs76593183 | snp | C/T | 0.16846 | 0.236329 | intron-variant | RNF216 | GRCh38.p7 | 7:5734374 | ACTATACAAAATCTT[C/T]ATGTAGTGTTCAAAA | 54476 |
rs76593446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF216 | GRCh38.p7 | 7:5717405 | ACAGACTTCGCTGGC[A/G]AGGCTGTGTGGTAGT | 54476 |
rs76601521 | snp | G/T | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5644523 | CCCATTTTTTTTTTT[G/T]GAGACAGAGTCTCAC | 54476 |
rs76638665 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5768644 | TAGGTAATTCTGAAA[C/T]GTGAGAAATGAAGCA | 54476 |
rs76681999 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF216 | GRCh38.p7 | 7:5749051 | TCAGAAAAACAGGAC[C/T]TAACTCCAATGCCTT | 54476 |
rs76682240 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | RNF216 | GRCh38.p7 | 7:5768957 | TGAGCCACTGTGCCC[C/G]GCCAAAGCAACTTTT | 54476 |
rs76682418 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5677568 | GGACCATCCTAAGCA[A/C]TTTGGGCTTAACCAT | 54476 |
rs76683748 | snp | C/T | 0.111224 | 0.207945 | intron-variant | RNF216 | GRCh38.p7 | 7:5721797 | CAAATATACAAGGGG[C/T]TGAAGGAACAGTACC | 54476 |
rs76722717 | snp | C/T | 0.16028 | 0.233346 | intron-variant | RNF216 | GRCh38.p7 | 7:5709212 | TCCTGTGAGACAAGA[C/T]AGAAACCAGTCCCTT | 54476 |
rs76738281 | snp | A/T | 0.152334 | 0.230133 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5754334 | TTACTTAAAAAAAAA[A/T]TTTTTTTTTGTAGAG | 54476 |
rs76746554 | snp | C/T | 0.0295035 | 0.117819 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712107 | ACTCCTTGCATATAC[C/T]GATTTCCCTCCAGCC | 54476 |
rs76764453 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | RNF216 | GRCh38.p7 | 7:5708007 | GCCAGGATGACAGGT[A/G]GGAGCCACCATGCCC | 54476 |
rs76825164 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | RNF216 | GRCh38.p7 | 7:5651242 | CTCTTTTTTTTTTTT[A/G/T]AGTTGGAGTCTCGCT | 54476 |
rs76856090 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | RNF216 | GRCh38.p7 | 7:5636537 | TTCCTGGCCCTGCTG[C/G]TTAATTAAGCCAGAG | 54476 |
rs76868457 | snp | A/G | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5736638 | CGGCCGGGAAGAGGC[A/G]CTCCTCACTTCCTAG | 54476 |
rs76912071 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5679454 | CTGGTGCACACACAC[C/T]GTAACAAGTGTAACG | 54476 |
rs76922575 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF216, MIR6874 | GRCh38.p7 | 7:5712888 | GGCGAAAAGGCAAAG[A/G]AAAAAAAATCAATAC | 54476 |
rs77018051 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | RNF216 | GRCh38.p7 | 7:5706316 | CTGTTAGCAAAATGT[C/T]GTACAGCTGATCTCT | 54476 |
rs77039506 | in-del | -/AGTGCTTGTAGCCAG | | | intron-variant | RNF216 | GRCh38.p7 | 7:5769907 | CCAGGCTTGGTGGCG[-/AGTGCTTGTAGCCAG]GAGGCTGAGACAGAG | 54476 |
rs77085121 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5675472 | GCAAGACACCCTCTA[C/T]GAAAAATAAATTTAA | 54476 |
rs77092068 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | RNF216 | GRCh38.p7 | 7:5630873 | AAACCCTGGCACAGC[A/G]AGGTTGTGACCCAGG | 54476 |
rs77102772 | snp | A/C | 0.5 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5704321 | GGCAAAGACACTGCA[A/C]TGAGAAAGCAGGTGC | 54476 |
rs77144090 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF216 | GRCh38.p7 | 7:5778201 | CCTTACCTCATACCT[C/T]TTCCCCCCGCATTCA | 54476 |
rs77170567 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF216 | GRCh38.p7 | 7:5703234 | TTTGGTTCTTGTCAA[C/T]GCTACTTCCTGAATA | 54476 |
rs77230950 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF216 | GRCh38.p7 | 7:5637371 | GGGCAGGCTAGCTAA[A/G]GGTTTCACTGGGTCA | 54476 |
rs77235423 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5637078 | CTGTGGAGCTCTTCA[C/G/T]AGCTCCAGCTGAAAA | 54476 |
rs77248118 | snp | C/T | 0.119281 | 0.213102 | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5620416 | TGGCACGGCCCCTTG[C/T]TGGCTGGTCTGAAGA | 54476 |
rs77261483 | snp | G/T | | | intron-variant | RNF216 | GRCh38.p7 | 7:5771174 | GGAAAACATGACCTT[G/T]CTACTATATGATGCT | 54476 |
rs77269952 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | RNF216 | GRCh38.p7 | 7:5767585 | GAAATCTCAGCAAAC[A/G]TGTATTGTTGAGAGG | 54476 |
rs77271156 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF216 | GRCh38.p7 | 7:5719742 | AAATAATCACTTCAT[C/T]CATTTTTGAGAAAAT | 54476 |
rs77306167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF216 | GRCh38.p7 | 7:5692164 | TATTTGCTTGGGAGC[C/T]GGAAGAGGGAACTAT | 54476 |
rs77308135 | snp | A/G | 0.039522 | 0.134904 | intron-variant, downstream-variant-500B | RNF216 | GRCh38.p7 | 7:5652075 | TTAGGTCTCAGGCCA[A/G]CAGTTTCCTATAACA | 54476 |
rs77309054 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RNF216 | GRCh38.p7 | 7:5638324 | GATATTTAAATGGTG[C/T]TTCTAAATTTGTACA | 54476 |
rs77334863 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF216 | GRCh38.p7 | 7:5721458 | TACCACAATTTATTA[C/T]CTATTTCACTACTGA | 54476 |
rs77363346 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF216 | GRCh38.p7 | 7:5762831 | CATATAACATCTTTT[C/T]TCTTTCTTTTAAAGA | 54476 |
rs77374040 | snp | C/T | 0.110167 | 0.207236 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5676462 | CCCATCTGTGAGAAC[C/T]GTCGCTGGGGAACCC | 54476 |
rs77388463 | snp | A/T | 0.5 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5673861 | CTCTCTTTCTCTCAT[A/T]TTTTTTTTTTTTTTT | 54476 |
rs77434248 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | RNF216 | GRCh38.p7 | 7:5631972 | GATTTCATAAGAGGA[C/T]CCTGAGGCTCAGAAG | 54476 |
rs77457438 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5678789 | CACACAGAAGGTGAC[A/G]GAGCAGATTTCTCGA | 54476 |
rs77457979 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | RNF216 | GRCh38.p7 | 7:5706983 | AGCGTCTAAGTTCAT[G/T]CTTTTGCATGTGGAT | 54476 |
rs77462745 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | RNF216 | GRCh38.p7 | 7:5758861 | AGACTTTGGGGACTG[C/T]TGGGAAGACGCAATT | 54476 |
rs77469878 | snp | A/T | 0.084364 | 0.187256 | intron-variant | RNF216 | GRCh38.p7 | 7:5731258 | TAATAAATGAAATAT[A/T]AAAGACCTTCTGTTA | 54476 |
rs77480997 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5680287 | GGTTCCTTTGTCCCC[C/T]GCCCTGCCCCCAGCT | 54476 |
rs77494326 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | RNF216, LOC107986762 | GRCh38.p7 | 7:5620048 | GACGAAGCTGGAGGG[A/G]GCAGAGCGCACAAAC | 54476 |
rs77494854 | snp | A/C | 0.000118723 | 0.00770371 | intron-variant, downstream-variant-500B | RNF216, MIR6874 | GRCh38.p7 | 7:5711716 | TGAGGGCAGCCCATA[A/C]TACCATAATTCAATA | 54476 |
rs77500990 | snp | C/T | 0.00325823 | 0.0402306 | synonymous-codon | RNF216 | GRCh38.p7 | 7:5725403 | ACTGGTTTCTGGTGA[C/T]AGCTCCTGCCATTTT | 54476 |
rs77520428 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF216 | GRCh38.p7 | 7:5774991 | CTCAGGTGATCCACC[C/T]CCCCGACACTCACCA | 54476 |
rs77533950 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5682289 | CCTCAGAGGCTACTT[A/G]ACCAGGTTACCCTCA | 54476 |
rs77534297 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RNF216 | GRCh38.p7 | 7:5659279 | GTTAGGCTCAGTTTC[C/T]ATCTTCATGACATTT | 54476 |
rs77573249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5664346 | TTACTGTCCTTCCTT[C/T]CTTTGCTCCCTAATG | 54476 |
rs77596366 | snp | G/T | 0.5 | 0 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5675727 | TTCTTTTTTTTTTTT[G/T]AGGTGGAGTTTCGCT | 54476 |
rs77599246 | snp | A/G | 0.129664 | 0.219133 | intron-variant | RNF216 | GRCh38.p7 | 7:5725969 | ACTGACAGATTAAAG[A/G]GTAACTAGGGAAAAG | 54476 |
rs77606809 | snp | C/T | 0.110872 | 0.20771 | intron-variant | RNF216, RNF216-IT1 | GRCh38.p7 | 7:5675059 | ACAGAATGGCAACTG[C/T]TGAAAAGCCAGCTTC | 54476 |
rs77608856 | snp | A/C | 0 | 0 | intron-variant | RNF216 | GRCh38.p7 | 7:5770027 | TGAGACCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 54476 |