SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15700 | snp | A/G | 0 | 0 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871570 | ACCAGCGTGTGAAAA[A/G]GGAACGAGAGAAGGA | 9886 |
rs750593 | snp | C/T | 0.44333 | 0.158505 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902556 | TTTGGTAATGCCTTT[C/T]GTGAATGAGTATTCT | 9886 |
rs873602 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002079 | ACACGACAGGACCAT[A/G]TGTAACGACTAAGTA | 9886 |
rs884403 | snp | C/T | 0.475613 | 0.107697 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898101 | GTCAATGATGACATA[C/T]AAAGAGGTGGGATCC | 9886 |
rs884404 | snp | C/T | 0.496034 | 0.0443518 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898080 | GGTGGGATCCTACCA[C/T]GGAACAAAAGAATTT | 9886 |
rs957854 | snp | C/T | 0.454544 | 0.143743 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937884 | GAGAGCTAACCCTTA[C/T]TGAGCACCTACTATG | 9886 |
rs1013704 | snp | C/G | 0.0948562 | 0.196037 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937660 | ACTTTGGCAACCTTA[C/G]AGTGTGAAGAAAACA | 9886 |
rs1013705 | snp | A/C | 0.11963 | 0.213316 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937764 | TATAACCATTCCTTA[A/C]AATATCAGAATTCAA | 9886 |
rs1864756 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949804 | ACTAACAATGAAAAG[A/T]ACACAGTATCTAATG | 9886 |
rs1864757 | snp | A/T | 0.482979 | 0.0906686 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949689 | CCAAAGTTATGCTTT[A/T]AAAAAAAAAAAAAAA | 9886 |
rs1864763 | snp | A/T | 0.478188 | 0.10213 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916923 | GAGAGAAATATGAAG[A/T]TGCTATACTGCTGGC | 9886 |
rs1864764 | snp | A/G | 0.498009 | 0.0314867 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917222 | TTCTAAATGTTGTTT[A/G]TTACCTTTATATACA | 9886 |
rs1897358 | snp | C/G | 0.480302 | 0.0972668 | | | GRCh38.p7 | 10:60970907 | TTTTTCTGATACTGA[C/G]TTTGACTCTCCATGA | 9886 |
rs1897359 | snp | A/G | 0.480302 | 0.0972668 | | | GRCh38.p7 | 10:60970687 | TCTGACCACGGAACT[A/G]TTAAAAAGTATTTGA | 9886 |
rs1897360 | snp | A/C | 0.0356815 | 0.128715 | | | GRCh38.p7 | 10:60957431 | cagcacatacgacag[A/C]ggtcccataacatta | 9886 |
rs1897363 | snp | A/G | 0.480382 | 0.097079 | | | GRCh38.p7 | 10:60975711 | AGCAGGAACAAAATG[A/G]TTTTTCAGTTTTTCC | 9886 |
rs1897364 | snp | C/T | 0.00835141 | 0.0640778 | | | GRCh38.p7 | 10:60976759 | ATAATAAAAATATTT[C/T]CTTTAAATTCACATC | 9886 |
rs1897366 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 10:60901394 | TGCCAATTATTATCA[A/G]ACAAATATAATTATG | 9886 |
rs1897367 | snp | A/G | 0.404907 | 0.196224 | | | GRCh38.p7 | 10:60906635 | CTATTTTGCAGGCTC[A/G]CCACAAGAGTGAAGC | 9886 |
rs1897368 | snp | C/T | 0.115788 | 0.21092 | | | GRCh38.p7 | 10:60930657 | TTATGAATAGAGAGG[C/T]ATGGCTTACCTCACC | 9886 |
rs1897369 | snp | A/G | 0.450231 | 0.149691 | | | GRCh38.p7 | 10:60938206 | ACCCACCATATCTTT[A/G]CACGACTGGAATTCT | 9886 |
rs1897370 | snp | C/T | 0.489376 | 0.0721049 | | | GRCh38.p7 | 10:60972930 | CACTGCACTTGTTTC[C/T]ATTTAAAAGGGGAGT | 9886 |
rs1946591 | snp | C/T | 0.490175 | 0.0693959 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967182 | TGCTATTCCCTTGCC[C/T]GGACTACTACTCTTT | 9886 |
rs1946592 | snp | C/T | 0.497586 | 0.0346604 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925972 | gtggtgtctcacacc[C/T]gtaatcctagcactt | 9886 |
rs2001940 | snp | C/T | 0.422473 | 0.180978 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897775 | GAAGTGGCTCAATCT[C/T]GGCTCACTGCAACCT | 9886 |
rs2082307 | snp | A/G | 0.492037 | 0.0625946 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990908 | CTCCCGTGATGTCTC[A/G]AGACATCTCAAACTC | 9886 |
rs2116452 | snp | G/T | 0.490618 | 0.0678448 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955371 | AATTGAATTGTGGCA[G/T]TTTAAAACCATAAAG | 9886 |
rs2116453 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000374 | CACCAGATCTGGGAA[A/G]AAACCCAAAATATAT | 9886 |
rs2163602 | snp | A/G | 0.498158 | 0.0302955 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985524 | ACATGTCAATTTCCT[A/G]TACAAAATGCTACGC | 9886 |
rs2271126 | snp | A/G | 0.325785 | 0.238236 | utr-variant-5-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60911547 | TCAGCGTCCATTTAT[A/G]AAACTCTGTAAGAAG | 9886 |
rs2271127 | snp | A/G | 0.153665 | 0.230694 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911616 | AGCAATCAAAGACGT[A/G]AGAGGTTCAGGGAGT | 9886 |
rs2271128 | snp | A/G | 0.088636 | 0.190949 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886115 | GAAGGCACGTACCTC[A/G]CTGTTGGCACTTTCC | 9886 |
rs2279942 | snp | A/G | 0.470618 | 0.117591 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874863 | TGCATCTGTCTAAAT[A/G]AAGATGTCACCACTG | 9886 |
rs2393707 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903025 | TTTCCCGCAATACAG[C/T]TATTGCTACGATAGG | 9886 |
rs2393708 | snp | C/T | 0.479824 | 0.098392 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984032 | CTGAAAACTATACCA[C/T]TTAAAATCTCTCTAA | 9886 |
rs2393709 | snp | C/G | 0.497855 | 0.0326773 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996634 | AAAAGCTCTGGACGT[C/G]CTCCTGAGAAAAATG | 9886 |
rs2393712 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955043 | TTCTTttctttcctt[C/T]ttttttttttttttt | 9886 |
rs2893866 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894322 | GAGATTAAAATATTT[C/T]CAAATTATAAGAGAG | 9886 |
rs2893868 | snp | A/G | 0.444267 | 0.157354 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901367 | CAGTGAAAGTGTTCT[A/G]TAACCGTTAAGTGCC | 9886 |
rs2893869 | snp | C/T | 0.44306 | 0.158832 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902203 | GAATGGTACATGTAT[C/T]TTCTGTGCGCCAGAT | 9886 |
rs2893870 | snp | A/G | 0.330482 | 0.236691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902893 | AACTAACATCGATCA[A/G]GCTCCTACAAGACAC | 9886 |
rs2893871 | snp | A/G | 0.338523 | 0.233803 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903023 | ATTTTCCCGCAATAC[A/G]GTTATTGCTACGATA | 9886 |
rs2893872 | snp | G/T | 0.444533 | 0.157025 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989359 | ATGAATTTATTTCAT[G/T]GCATAAGTATATTTT | 9886 |
rs2893873 | snp | C/G | 0.480775 | 0.0961398 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993688 | AAAATATACACCGTA[C/G]AGCAATATAAAATGT | 9886 |
rs2893874 | snp | C/T | 0.480382 | 0.097079 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963327 | GCTCCCAATTTCAGA[C/T]GATGAAAGTGAATTT | 9886 |
rs3049417 | in-del | -/CAC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881017 | agctcccataattcc[-/CAC]gtgttgtgggagaga | 9886 |
rs3049452 | in-del | -/TG | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997104 | gtgtgtgtgtgtgtg[-/TG]TACATAACCATGCTG | 9886 |
rs3049595 | in-del | -/TTT/TTTT/TTTTT/TTTTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932513 | ttttttttttttttt[-/TTT/TTTT/TTTTT/TTTTTT]actttAAGAAAGtat | 9886 |
rs3049597 | in-del | -/GACTTCAA | 0.0948562 | 0.196037 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930998 | GAGGGAAGACTTCAA[-/GACTTCAA]TATTGCTTCCTGTTA | 9886 |
rs3763742 | snp | C/T | 0.220843 | 0.248294 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870857 | TACCAGCACTTAACA[C/T]GGCAAATATTGTAAA | 9886 |
rs3999424 | in-del | -/TTTT | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955062 | ttttnntttttttnt[-/TTTT]nnnaagatgtagtct | 9886 |
rs4072139 | snp | C/G | 0.475348 | 0.108251 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897598 | AAGTTCTCCAGAAAG[C/G]TATGAGTGGGACAGC | 9886 |
rs4309112 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955500 | CTTCCTTCTGATTGA[A/G]CAGGGTAATTATTCA | 9886 |
rs4339988 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947110 | ACAGACCGTATTTTG[C/T]TAATAGGAAAAGAGA | 9886 |
rs4376852 | snp | G/T | 0.479744 | 0.0985793 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927502 | aaaagcatgggacag[G/T]cataaaaacagacac | 9886 |
rs4408258 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929978 | GGCCCCAAATCCCCC[A/G]AAGTGTAAATTGTTG | 9886 |
rs4437981 | snp | C/T | 0.44252 | 0.159487 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902745 | CAGGTTGATCCATCA[C/T]TTGTTATTCTTATTA | 9886 |
rs4472883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955524 | TTATTCAAGGAGTAT[C/T]TGTCCTGAGCTATCC | 9886 |
rs4485055 | snp | A/G | 0.4231 | 0.180378 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913297 | ATTCAAGGAACAGAT[A/G]TGTGCTTAGGTTAGG | 9886 |
rs4542350 | snp | C/G | 0.0952156 | 0.196321 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937947 | tcataaccctctgag[C/G]ggggaggggatgctg | 9886 |
rs4545506 | snp | C/T | 0.422 | 0.181428 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902761 | TTGTTATTCTTATTA[C/T]AAAAGGGCATATATA | 9886 |
rs4545508 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938125 | TAGAAGGGTGTTATG[C/T]TTTGAATAAGAGAAA | 9886 |
rs4575214 | snp | C/T | 0.345037 | 0.231231 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902710 | GGCTAAGCACCAGTA[C/T]TTTCCATCTTCATCA | 9886 |
rs4582920 | snp | C/G | 0.497586 | 0.0346604 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942981 | CTGGAGTTCAACAAG[C/G]CTCAGTGAACAGCAC | 9886 |
rs4641412 | snp | C/T | 0.434687 | 0.168495 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902887 | TCGTTCAACTAACAT[C/T]GATCAAGCTCCTACA | 9886 |
rs4643024 | snp | A/G | 0.4973 | 0.0366419 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933780 | GTCCAAACACAGGAG[A/G]TGGATTAAAAAAAAA | 9886 |
rs4948437 | snp | C/T | 0.380333 | 0.213338 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973559 | GGAGGGCAAAGCTTG[C/T]TGAGTTTCATATTCA | 9886 |
rs5785469 | in-del | -/AAAA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932529 | AAAAAAAAAAAAAAA[-/AAAA]AAAGACAGAAACAAG | 9886 |
rs5785470 | in-del | -/C | 0.490727 | 0.0674567 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951345 | ATAATGGTTCCTAAT[-/C]TAAAAGCAAAGATGA | 9886 |
rs5785471 | in-del | -/AC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997065 | ACAGCATGGTTATGT[-/AC]ACACACACACACACA | 9886 |
rs6479741 | snp | G/T | 0.101763 | 0.201681 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885169 | aaatagctaaaagac[G/T]attttaaatgttctc | 9886 |
rs6479743 | snp | C/T | 0.489318 | 0.0722982 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971083 | TCATCATTATCATTA[C/T]TGATGTAATTAATAA | 9886 |
rs6479744 | snp | C/T | 0.497329 | 0.0364438 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989635 | TGCCTTAGCACCTTG[C/T]TTCCTGTGCTGAGAC | 9886 |
rs7067621 | snp | A/T | 0.405255 | 0.195948 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907223 | TACCAGTGTAAGAAC[A/T]GACTAATACAGGGAC | 9886 |
rs7068842 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930841 | GGGCTAGCCATCATT[C/T]TCTGCTTGTCTTATT | 9886 |
rs7069036 | snp | A/T | 0.4944 | 0.0526182 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891713 | CAAAAAGTTCAACAT[A/T]AAAAAAACATAAAAA | 9886 |
rs7073034 | snp | C/T | 0.139903 | 0.224452 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873693 | CTGTTTCAAAAGACC[C/T]CAAATTCCAAGTGTG | 9886 |
rs7073240 | snp | C/T | 0.497613 | 0.0344622 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931542 | TGGCTGAAAAATATT[C/T]TTAGACATATTACTT | 9886 |
rs7073817 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874019 | CTCTGGCCACAGTAG[A/G]AAGGGCCTGAGCAGC | 9886 |
rs7074600 | snp | A/G | 0.495708 | 0.0461266 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896540 | GAACCTGAATACTGA[A/G]AAGGGGTAGGAAGGA | 9886 |
rs7074883 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896686 | GCTTGCCCTTGCCCA[C/T]GGAATGTTTATATCT | 9886 |
rs7077303 | snp | C/T | 0.489376 | 0.0721049 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993885 | TAGTAATTAATTTTT[C/T]GGTGACATTTAGCTC | 9886 |
rs7078521 | snp | A/T | 0.0988009 | 0.199095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893627 | GTAATATTTAACATA[A/T]AACTAGGCGAGAATT | 9886 |
rs7078938 | snp | A/T | 0.437965 | 0.164831 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883180 | CAGGTCTTCAGTGGC[A/T]TGGTTCCGTGGTCTT | 9886 |
rs7079085 | snp | A/G | 0.494609 | 0.0516363 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897247 | TGGTGGGAAAAGATC[A/G]GAGAAGCAACCAGAA | 9886 |
rs7079357 | snp | A/T | 0.428333 | 0.175206 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883410 | TGGAGACGATTACAG[A/T]CCATTCTTGGAAGGG | 9886 |
rs7081336 | snp | C/T | 0.443732 | 0.158012 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880730 | ACACAGATGTTGGAA[C/T]ATTATTCTTCCCTTC | 9886 |
rs7082246 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875471 | tgaaatgtttccatc[A/T]ctgcagaaagttcta | 9886 |
rs7083122 | snp | A/C | 0.416055 | 0.186885 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875947 | TCATCTGTAGCATTG[A/C]ATTTGTTCTTCTAAT | 9886 |
rs7083267 | snp | G/T | 0.491525 | 0.0645418 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894573 | AAGCCAAGAATGCTT[G/T]GAATTTTACATTTTT | 9886 |
rs7083452 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903681 | CTGGGTCAGACTATG[A/G]GCCCCTGGGTCAGAC | 9886 |
rs7084092 | snp | G/T | 0.480144 | 0.097642 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972202 | gagtttatacccaaa[G/T]gattataaaccattc | 9886 |
rs7084565 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989034 | TTCAATGCTCTAAAA[A/G]TTATAGGAGATTAAA | 9886 |
rs7085867 | snp | C/T | 0.488545 | 0.074807 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960257 | AAGTGAAAAATCTAA[C/T]TAAATGATGCTTCCA | 9886 |
rs7087218 | snp | A/G | 0.472335 | 0.114312 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876352 | TAATAACTAAACTAA[A/G]TGTTCATAGAAGTCT | 9886 |
rs7087304 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876639 | GTAATTGCCCATGGA[A/C]gcctcccagagtgag | 9886 |
rs7087599 | snp | G/T | 0.210301 | 0.246828 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904255 | CCTGGCCTATTTCTC[G/T]TCTTAAAGAATTTTT | 9886 |
rs7089016 | snp | C/T | 0.489434 | 0.0719116 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885424 | GGCTGACAAGTGATG[C/T]AGCTGCTTCCGCTAG | 9886 |
rs7089671 | snp | A/C | 0.467337 | 0.123551 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892581 | TTAGAGAATTTACTT[A/C]AAGTGCTGTCCAATC | 9886 |
rs7090226 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913908 | AGGTTGTTGTGAGGA[C/T]TACGTGAACTGATGA | 9886 |
rs7091298 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883076 | AGTATATTATAGTTT[A/T]CACAGGAAATAAAGT | 9886 |
rs7091617 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874057 | GGATGCCACCTCCTC[G/T]CCCTGAAACCACCTC | 9886 |
rs7093952 | snp | A/C | 0.493386 | 0.0571263 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893384 | TTTCACCAGTTTAAA[A/C]AACATAAAGGTGATG | 9886 |
rs7094320 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893609 | ACTAAGTAAGGCAAG[A/T]AGGTAATATTTAACA | 9886 |
rs7095485 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971276 | agctggaggcatcac[A/G]ctacctgacttcaaa | 9886 |
rs7095659 | snp | A/C | 0.480382 | 0.097079 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971542 | cttatacaaaaatta[A/C]ctcaagatggattaa | 9886 |
rs7097615 | snp | A/G | 0.448452 | 0.152042 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899335 | CTCTCTTTCAACTCC[A/G]TCTGGAGTTCATATT | 9886 |
rs7099056 | snp | C/T | 0.470132 | 0.118498 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894516 | GTGAAATATTCTGCG[C/T]TCAGTCTTACTTACA | 9886 |
rs7342040 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990985 | ctccaccattgttcc[C/T]TGACACTTCCTCATG | 9886 |
rs7477010 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992734 | GTTATGAATGCACTT[C/T]TGCAATTATGAGAGT | 9886 |
rs7478165 | snp | A/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929558 | TTTAAAGAACTATGG[A/T]AACCAAAGCCAAAAA | 9886 |
rs7478290 | snp | A/T | 0.184521 | 0.241273 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880202 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 9886 |
rs7894065 | snp | G/T | 0.49533 | 0.0480965 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898653 | CTGGATGTGAGCAGA[G/T]AAATCAAGTTAATAC | 9886 |
rs7897620 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961204 | TTACACTCAAAATAG[A/G]GCTCACAAAAATGTC | 9886 |
rs7898435 | snp | C/T | 0.492966 | 0.0588865 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892407 | CTTCAATATGTGTGT[C/T]TGTATGAATCTGATG | 9886 |
rs7898439 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892423 | TGTATGAATCTGATG[C/T]TCTCTGGGGCCCAGA | 9886 |
rs7898582 | snp | G/T | 0.489024 | 0.0732638 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952739 | GCTCATCTTAAATTC[G/T]GATATTAAACTCAGG | 9886 |
rs7904845 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975115 | AGCTAATGAACTATA[C/T]TGACTGATTGCTGTA | 9886 |
rs7907851 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999043 | taTTGTGGCACAGTG[C/T]CTAGTATATCACAGC | 9886 |
rs7908589 | snp | C/T | 0.470521 | 0.117772 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898546 | CAGGAGATGAATGGC[C/T]GTGTAAGCTCATACT | 9886 |
rs7909778 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946219 | TTCCCTTAGTATTTT[A/G]CAAAATGACTCCATC | 9886 |
rs7909783 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946226 | AGTATTTTGCAAAAT[A/G]ACTCCATCTTGAAAG | 9886 |
rs7913287 | snp | A/G | 0.497695 | 0.0338674 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922411 | AAGTAGCCTTAGTCT[A/G]TATGGAGCCTCTACA | 9886 |
rs7913431 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922550 | GACTGCCATGTCCAC[A/G]GGGAAAAGAATTGGC | 9886 |
rs7913710 | snp | G/T | 0.497668 | 0.0340657 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922783 | CAAAGTATGGAAAAA[G/T]ATTCTCTCTGTTCTG | 9886 |
rs7914393 | snp | C/G | 0.485731 | 0.0832509 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947550 | gactgttatattaat[C/G]ggaacataagtatgt | 9886 |
rs7914882 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947754 | tttgagtagtttcca[A/G]tattttgctattaat | 9886 |
rs7916014 | snp | C/G | 0.490175 | 0.0693959 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965467 | GTGTTTGTATTGTTG[C/G]TATCATGATTCTTCC | 9886 |
rs7917689 | snp | C/G | 0.11228 | 0.208646 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983697 | GTGAGCATGTAATAA[C/G]CCCCTAAAGATAGTT | 9886 |
rs7919957 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957155 | aggctgtttgacact[C/T]aacttaaaatatata | 9886 |
rs7920871 | snp | A/C | 0.0887219 | 0.191022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871933 | AGGGGAAGGCCACCA[A/C]CTCTGCACTCTCTGC | 9886 |
rs7920892 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871960 | CTGCAACAGGGCACC[C/T]TGGACTCTAGCCCAC | 9886 |
rs7923774 | snp | A/G | 0.0973687 | 0.197999 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884851 | gggtgaatggggaaa[A/G]gaaagccatctgtca | 9886 |
rs9633554 | snp | G/T | 0.173965 | 0.238157 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997381 | ATTCAGAACTGTGCA[G/T]AATGGCTCCAAGCAA | 9886 |
rs9665346 | snp | A/C/T | 0.00107063 | 0.0231124 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886144 | CCACAAATGACCCCC[A/C/T]GAACATGGCTGCCAT | 9886 |
rs9787551 | snp | C/G | 0.0807149 | 0.183963 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945271 | CTGTGTTCAGCTACC[C/G]AGAGGAATGAATATA | 9886 |
rs9787690 | snp | A/G | 0.483199 | 0.0901004 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945394 | AGGTAATGTGTTCCT[A/G]AGATACTGAAGGACT | 9886 |
rs10082373 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886727 | AGATGTGGGGGGGGG[G/T]GGGTCTGGCTATGTT | 9886 |
rs10082527 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886718 | TTTTTTAAGAGATGT[C/G/T]GGGGGGGGTGGGTCT | 9886 |
rs10082528 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886726 | gagatgtgggggggg[G/T]tgggtctggctatgt | 9886 |
rs10430493 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925579 | gaattaataaagatc[A/G]gagcagaaataaatg | 9886 |
rs10509141 | snp | A/G | 0.348354 | 0.22984 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900534 | GCTGTCTTTTCCACC[A/G]TACTATGAGGTCATT | 9886 |
rs10538288 | in-del | -/ACTCTA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953979 | TTTAAATTTACTTTA[-/ACTCTA]TTCCATGTTATTGTG | 9886 |
rs10571830 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881018 | GCTCCCATAATTCCC[-/A]CGTGTTGTGGGAGAG | 9886 |
rs10761563 | snp | C/T | 0.334412 | 0.235318 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913829 | TTTGGGCAAGTTGTT[C/T]GTACTTTCTGAGCCT | 9886 |
rs10761564 | snp | G/T | 0.499673 | 0.0127754 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947590 | AGATTGACTTTTTTT[G/T]TTTGTTTGTTTTTTT | 9886 |
rs10761565 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950773 | ACAATGCTGTGCAGC[A/G]TAGGGTATCATTTGA | 9886 |
rs10821848 | snp | C/T | 0.451608 | 0.147832 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879024 | TAAGATTTCCACACA[C/T]ATTCTTTAATTTGAT | 9886 |
rs10821849 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880204 | gtgtgtgtgtgtgtg[A/T]gagagagagagagag | 9886 |
rs10821850 | snp | C/G | 0.445592 | 0.155704 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880360 | TGTGGCTCCAGAGCT[C/G]TTTAAGCTATAGAAA | 9886 |
rs10821851 | snp | C/T | 0.439918 | 0.162576 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901153 | GCATAGTCAAGATGA[C/T]ACATTGAAAAAAGAA | 9886 |
rs10821852 | snp | A/C | 0.439918 | 0.162576 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901181 | GAATTCACTAATGTG[A/C]TTTCTGTGTCTGCAA | 9886 |
rs10821853 | snp | A/C | 0.441158 | 0.161117 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901299 | AAGTCTAATCATGGC[A/C]AATATTAGAAATTAC | 9886 |
rs10821855 | snp | C/T | 0.328616 | 0.237317 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904997 | TTTCCATAAAAAGCA[C/T]ATGCATTGCTAACTT | 9886 |
rs10821856 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906173 | GGGATAAGGGCAAGT[A/G]CAGTGGTTCTGAATG | 9886 |
rs10821857 | snp | C/T | 0.292008 | 0.246445 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913813 | TTTCCAGTCATTGGA[C/T]TTTGGGCAAGTTGTT | 9886 |
rs10821858 | snp | C/T | 0.427879 | 0.175668 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913996 | TGCTGAAGACGAATG[C/T]CTTCAGATGACAACA | 9886 |
rs10821860 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928246 | AGCACGGCCATTTTG[C/G]AAAACTATATGGATG | 9886 |
rs10821861 | snp | A/C | 0.482234 | 0.0925596 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956960 | TTACAGCTTGAAAAA[A/C]CAACATATCGCTGTC | 9886 |
rs10821862 | snp | C/G | 0.482234 | 0.0925596 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956961 | TACAGCTTGAAAAAC[C/G]AACATATCGCTGTCT | 9886 |
rs10821863 | snp | A/C | 0.499218 | 0.0197529 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957081 | ATAACATATATGGAG[A/C]TGTCCTCTCCTATGA | 9886 |
rs10821864 | snp | A/C | 0.479984 | 0.0980171 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982989 | CCATGGTCTTTTAAT[A/C]GACAGATTAATTCCA | 9886 |
rs10821865 | snp | A/T | 0.481319 | 0.0948228 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991271 | CCACCAAAAAAACGA[A/T]AAACAACAAAAATCC | 9886 |
rs10821866 | snp | A/C | 0.488118 | 0.0761554 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991377 | GATGACATCCCCAGA[A/C]TTAAGCAGTTCACTC | 9886 |
rs10994554 | snp | C/G | 0.103082 | 0.202275 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873119 | CAGAAACCCACTCAA[C/G]AGACTCACTGAAAAT | 9886 |
rs10994556 | snp | C/T | 0.450105 | 0.149859 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877357 | TTATATTTTAACTCA[C/T]TTAATCTCCATAACA | 9886 |
rs10994557 | snp | A/T | 0.101301 | 0.200969 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878953 | GGATTTTTGGAACAT[A/T]GACAATTATAAACAT | 9886 |
rs10994559 | snp | A/T | 0.110872 | 0.20771 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882253 | TGCTACCCTAAACAA[A/T]GTTCTATCTTGCAGT | 9886 |
rs10994560 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885140 | TGGTGGACAATAATG[G/T]ATCGTATATTTCAAA | 9886 |
rs10994561 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887196 | GTTTAAGTTACTGTA[A/G]GTTTGTAACATATTC | 9886 |
rs10994562 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895467 | TGGAGTGCACTGGCA[C/T]GATCTCAGCTCACCA | 9886 |
rs10994564 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897878 | cctggctaatttttt[C/G]tatttttagtagaga | 9886 |
rs10994565 | snp | C/T | 0.46974 | 0.119223 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899120 | ATTTTCTATACTTGG[C/T]AAATCATACTCCCGT | 9886 |
rs10994566 | snp | C/T | 0.461481 | 0.133325 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899133 | GGCAAATCATACTCC[C/T]GTTAGTTTATTCTTA | 9886 |
rs10994567 | snp | A/G | 0.285519 | 0.247464 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904469 | AGTGATCTACTTTCC[A/G]TCACTATAGATTAGA | 9886 |
rs10994568 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905089 | GAAGAAAATGAAGCA[C/T]TTCTTCAAGTGCAAA | 9886 |
rs10994569 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905349 | tagctacttgggagg[C/T]tgaggcaggagaatc | 9886 |
rs10994570 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905447 | agtgagagactcttt[C/T]tcaaaaaaaaaaaaa | 9886 |
rs10994571 | snp | A/G | 0.401215 | 0.199083 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905574 | GTCTGAGGCAGAAGG[A/G]AAAAAAAAACCAAAA | 9886 |
rs10994572 | snp | G/T | 0.278133 | 0.248412 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905702 | CACCTCCTGGTCCAC[G/T]TGAAGTTTCACTGTG | 9886 |
rs10994574 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908086 | CCATTTAAATCATAA[C/G]AGAGCAATAACACTG | 9886 |
rs10994576 | snp | G/T | 0.498034 | 0.0312882 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917516 | TAGGTTCTGGTGAGG[G/T]CTCTCTTCCTGGCTT | 9886 |
rs10994578 | snp | C/T | 0.497613 | 0.0344622 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931941 | CAAAAGGAATACTTA[C/T]GGTAACTGAAATGAG | 9886 |
rs10994579 | snp | A/G | 0.477853 | 0.102875 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943869 | CTCGTGGCACGGCCC[A/G]GGGCCCCCACTTGCC | 9886 |
rs10994580 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950082 | AATTTGTCCTACCAA[A/G]ATGGTGTTCCACTGG | 9886 |
rs10994581 | snp | C/T | 0.490782 | 0.0672626 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956168 | TGCAAACCTGTACAG[C/T]ATGTTACTGGATTGA | 9886 |
rs10994582 | snp | G/T | 0.490727 | 0.0674567 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956842 | TTAGAAAGCATTCCC[G/T]CCATCTAAATTTGTG | 9886 |
rs10994583 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962588 | ATAGTATTTTTTTCT[A/G]TATAAAATAATTTTC | 9886 |
rs10994584 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967779 | GGCAAAGAGACAATG[C/T]TGGTGTTTCTATATT | 9886 |
rs10994586 | snp | A/T | 0.489434 | 0.0719116 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974305 | CTGGGTTCATGACTA[A/T]TTACATACTCTGACT | 9886 |
rs10994587 | snp | G/T | 0.489434 | 0.0719116 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978191 | CAAAACTGAGCTGAG[G/T]CTTTTTATTTAATTT | 9886 |
rs10994588 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980297 | TGGAAGAGAGAATTC[A/T]ATACAAAAATCAATA | 9886 |
rs10994589 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981072 | TTACTGGGAAATTCT[A/G]TGTTTGATATGTAAG | 9886 |
rs10994590 | snp | C/T | 0.488905 | 0.0736498 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983830 | CCCTGCAGAGCTTCC[C/T]GGCCCCGCCCTCCTT | 9886 |
rs10994591 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987482 | CATAACCAATGATTA[A/G]ATTATGGCCACCTTG | 9886 |
rs10994592 | snp | A/G | 0.488726 | 0.0742286 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987995 | ATGGAGTGCACTGGC[A/G]CGATCTCAGCTCACT | 9886 |
rs10994594 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989337 | AAAATGCATTTGAGA[C/T]TATCACATGAATTTA | 9886 |
rs10994595 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989723 | AAGCAGGAAGGAAAA[C/T]TGAGGCTGTAGCTCA | 9886 |
rs10994596 | snp | A/C | 0.479583 | 0.0989539 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989973 | CCTCAGAACCTCAGA[A/C]TGTCCTTTTTTTTTT | 9886 |
rs10994597 | snp | A/G | 0.480775 | 0.0961398 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990132 | GGACTACAGGCGCCC[A/G]CCACCACGCCTGGAT | 9886 |
rs10994598 | snp | A/C | 0.477853 | 0.102875 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990146 | CGCCACCACGCCTGG[A/C]TAATTTTTTGTATTT | 9886 |
rs10994599 | snp | C/G | 0.489665 | 0.0711382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990265 | TGGGATTACAGGCGT[C/G]AGCCACCGTGCCCGG | 9886 |
rs10994601 | snp | C/T | 0.481627 | 0.0940692 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991159 | ACTGATATGCATACT[C/T]TTCCCCCTTGCCAAC | 9886 |
rs10994602 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992526 | CCTTTTTATATCTTA[G/T]CTTCTAAAATTTATG | 9886 |
rs10994603 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992605 | CTAGCAACTGTATCA[G/T]GATCTCAATAAATAG | 9886 |
rs10994604 | snp | C/T | 0.488905 | 0.0736498 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996132 | CTCTTACCAGGCTGA[C/T]TGACTCTGGAGCTTG | 9886 |
rs10994605 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000148 | TAATCCTTACGCTTC[C/T]GAGTGCATCTGACAG | 9886 |
rs10994606 | snp | A/C | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000824 | TCAATAAATCAAAGT[A/C]TAGTTCTTGACCCAA | 9886 |
rs10994607 | snp | C/T | 0.149999 | 0.229128 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000984 | AGCCCAGATTCTTAT[C/T]TTTTCTGACTGACAG | 9886 |
rs10994608 | snp | A/C | 0.141596 | 0.225274 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002812 | GCCTTTTAATGAATT[A/C]TTTCCTTTTCAATAT | 9886 |
rs11295111 | in-del | -/A | 0.479663 | 0.0987666 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989197 | GAGCAAATGAGAGAG[-/A]AAAAAAGTAGAAGTT | 9886 |
rs11304357 | in-del | -/A | 0.493925 | 0.054776 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893106 | TCTCATGTCACAATT[-/A]AAAAAAAAAAAGACC | 9886 |
rs11320147 | in-del | -/A | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967238 | TCTAAGACCAATTAG[-/A]AAAAAAAAATATAGC | 9886 |
rs11344569 | in-del | -/A | 0.496034 | 0.0443518 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946180 | AAGACTCCTTCTCAG[-/A]AAAAAAAAAAACAAA | 9886 |
rs11414207 | in-del | -/T | 0.417034 | 0.18601 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942859 | TATTTTTTTTTTTTT[-/T]CTGTTTAGAGTATGT | 9886 |
rs11593880 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940288 | CATTTCATTTTTTAG[C/T]ACCCCTTTATATAAA | 9886 |
rs11594559 | snp | C/T | 0.488965 | 0.0734569 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980992 | CTATATTAAAATATG[C/T]TAGAAAGATGTGTAC | 9886 |
rs11595278 | snp | A/G | 0.262159 | 0.249704 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916296 | ttcacattgaaaacc[A/G]ctgaggcagccctgc | 9886 |
rs11595841 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940289 | ATTTCATTTTTTAGT[A/C]CCCCTTTATATAAAA | 9886 |
rs11596880 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920956 | tttgttttttttttg[G/T]ttttttttttttatg | 9886 |
rs11812136 | snp | G/T | 0.139903 | 0.224452 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895457 | TTGCCCAGGCTGGAG[G/T]GCACTGGCATGATCT | 9886 |
rs11814898 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990626 | ctagaacccttgctc[C/T]tctgccccccatgac | 9886 |
rs12219009 | snp | A/G | 0.495483 | 0.0473088 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903455 | GACTGGGTACAAAAC[A/G]GAGGTCACGTGCATG | 9886 |
rs12220887 | snp | C/T | 0.490836 | 0.0670685 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953990 | TTTAACTCTATTCCA[C/T]GTTATTGTGGTTTAA | 9886 |
rs12221129 | snp | A/G | 0.10237 | 0.201756 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875451 | CTGTTTGGACCATCC[A/G]GATATGAAATGTTTC | 9886 |
rs12221173 | snp | C/T | 0.441295 | 0.160954 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903454 | TGACTGGGTACAAAA[C/T]AGAGGTCACGTGCAT | 9886 |
rs12242007 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910720 | TTCTTTTCTTGACAT[C/T]AGGAAACAATACCAT | 9886 |
rs12242633 | snp | C/T | 0.4776 | 0.103433 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896597 | TTATTAAATATTTTA[C/T]GTTTCACTGGGCTAA | 9886 |
rs12243758 | snp | A/T | 0.0741063 | 0.177655 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902160 | GCGCGAAGGACAGTG[A/T]GGGACAGCAGGCTGA | 9886 |
rs12246070 | snp | C/G | 0.42263 | 0.180829 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912347 | CAAGCGATTCGCCTG[C/G]CTCAGCCTCCTGAGT | 9886 |
rs12247875 | snp | A/G | 0.0908922 | 0.192833 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885529 | CCTCATATCCCCTCA[A/G]CACAGGCAGAGTCAG | 9886 |
rs12249564 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949609 | AGCTGGAAATTAACT[C/T]TTAGGTTTGCAGTCC | 9886 |
rs12249886 | snp | C/T | | | utr-variant-5-prime, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944098 | cccctgcgcgcggcg[C/T]gccgcccgccgcccA | 9886 |
rs12249908 | snp | C/T | 0.469642 | 0.119404 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889927 | TCTTCATCACCTTCA[C/T]CTTTATCAACAGCAT | 9886 |
rs12249956 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950003 | TTTTCTGTTGGGGTA[C/G]GGTGAGTTTGGTAAA | 9886 |
rs12251146 | snp | A/T | 0.153997 | 0.230832 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902853 | AGAAGATCCTGGAAC[A/T]CATGAGAGATTTGTC | 9886 |
rs12251212 | snp | A/G | 0.184707 | 0.241328 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875081 | AGAACATTAAACCAC[A/G]CCCTGCGAGCCAGGT | 9886 |
rs12251789 | snp | A/C/T | 0.0198089 | 0.0978352 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890527 | GTGCTGGGGTTATGG[A/C/T]ATAACCATGGCAAAG | 9886 |
rs12251974 | snp | A/G | 0.421368 | 0.182025 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890670 | CCTTTAACACCAAAG[A/G]TAATATATAGGACAG | 9886 |
rs12252953 | snp | A/G | 0.294064 | 0.246086 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903366 | TGGAGTCTCATGCCC[A/G]TGAGTCTAGTAACCA | 9886 |
rs12253738 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921232 | ggattaccagcatga[A/G]ccaccatgcctgATC | 9886 |
rs12259045 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999767 | TCCCTGTTAGGGAAT[A/G]TTTATGGTTCAGACA | 9886 |
rs12259264 | snp | A/G | 0.379942 | 0.213577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878655 | GTTATCAGTAGATTC[A/G]GAGAATCCAAAGGAC | 9886 |
rs12260432 | snp | C/T | 0.490673 | 0.0676508 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884400 | CCCATGTTTTCATTT[C/T]TACTTTTTTAAAAAA | 9886 |
rs12261045 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907153 | ccacacggaactgtg[A/G]gtccattaaacctct | 9886 |
rs12261549 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900594 | TTCTCTCTCATTGTG[C/T]GCACACAGTGTAAGG | 9886 |
rs12262806 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885863 | TGGCATGTAAAGCAC[C/T]CAGGTGCCCCCACAC | 9886 |
rs12263149 | snp | A/G | 0.494526 | 0.0520291 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001765 | TCCTACTGGGACCCC[A/G]GTCTTTGGACCTGGC | 9886 |
rs12263661 | snp | A/G | 0.432063 | 0.171327 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901562 | AGAATTATCCACTGA[A/G]GATATGCAGAATTAT | 9886 |
rs12265082 | snp | A/G | 0.356169 | 0.226336 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880039 | CTCTACAGATAAGTT[A/G]AAGTATACAGGAGGA | 9886 |
rs12265809 | snp | C/T | 0.426201 | 0.177351 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893616 | AAGGCAAGAAGGTAA[C/T]ATTTAACATATAACT | 9886 |
rs12266720 | snp | C/T | 0.37955 | 0.213815 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878278 | CCTGACACAGCCTGA[C/T]GTGGAATTTTTAAAT | 9886 |
rs12267306 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916013 | CAAAATTCCACTCTC[A/G]GAAAAAAAACTCCTA | 9886 |
rs12269234 | snp | C/T | 0.477853 | 0.102875 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900382 | GGTATAGCCTGAGGA[C/T]CAGATGTGTGATGTG | 9886 |
rs12354512 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905014 | TGCATTGCTAACTTT[C/T]TTCCCTTAGTTACTT | 9886 |
rs12354863 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905282 | agtgaaaccccagct[C/T]tactaaaaatacaaa | 9886 |
rs12355671 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972901 | GAGGCAAAATACCCA[C/T]TGATGTTAACAAAAC | 9886 |
rs12411699 | snp | C/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935329 | tacattgattgggta[C/G]tggctggataggggc | 9886 |
rs12413154 | snp | C/T | 0.497829 | 0.0328757 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935363 | agaagggcttctggg[C/T]gctggtaatgttctg | 9886 |
rs12413471 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975278 | GTTTTTAGGCCATGA[C/T]AACCTAATGCATTTT | 9886 |
rs12413712 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981159 | TTGAGGTAACAAATG[C/T]CATTTGAAGTTTCTC | 9886 |
rs12415189 | snp | C/T | 0.488485 | 0.0749998 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981144 | TAAGATTTTTGTTTA[C/T]TGAGGTAACAAATGC | 9886 |
rs12415223 | snp | C/T | 0.479744 | 0.0985793 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981407 | TGCCTGTTAAACAGA[C/T]GAAGAAACTGAGTGC | 9886 |
rs12569748 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870562 | GTCCAGGGACCTTTT[C/T]CCTTGCCCATCTCAA | 9886 |
rs12571380 | snp | A/T | 0.479583 | 0.0989539 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958427 | AGAAGTTAAAATTTT[A/T]CTTTTTTATTTGAAG | 9886 |
rs12763739 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913366 | ACAGTCAGATACCTG[C/T]CCACCTGACACATAC | 9886 |
rs12765334 | snp | A/C | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970308 | ATTTGAGTGGTAGTC[A/C]CAGCTTATATTCAGC | 9886 |
rs12765639 | snp | A/C | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996926 | TCTGGAGAACAAGGG[A/C]CTTCACTATTTCCTC | 9886 |
rs12766200 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956282 | taaaaaaatggtatg[C/G]ctgtatagggcattt | 9886 |
rs12766215 | snp | A/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986433 | TATATATATATATAA[A/T]ATATATATAGGCCAT | 9886 |
rs12766556 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956235 | gtgtatctaaacaca[A/G]aaaaggtacagtaaa | 9886 |
rs12766794 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970220 | ATTGGTTATTTGTGG[G/T]TACAAGTCTATTCCA | 9886 |
rs12766835 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970280 | TAATTTTGAGTACAG[G/T]GGGGCTTAGGTGATT | 9886 |
rs12766967 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986529 | AGGTGAAAGGAAAAC[A/G]AAGTCCTATTCTTAG | 9886 |
rs12769453 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949965 | TTACCTAAAGTCCTT[A/T]CTGTGTGGATTCATT | 9886 |
rs12769834 | snp | A/T | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944960 | TTGACTGTGGCCTCC[A/T]TGGGCTGTCTTGGTC | 9886 |
rs12771464 | snp | G/T | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944961 | TGACTGTGGCCTCCA[G/T]GGGCTGTCTTGGTCT | 9886 |
rs12772048 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932533 | aaaaaaaaaaaaaaa[A/G]acagaaacaagaaaC | 9886 |
rs12772620 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999255 | TTAGTGAAGGAAATG[A/G]AAAGAAAAGTCCACT | 9886 |
rs12772813 | snp | A/C | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999267 | ATGAAAAGAAAAGTC[A/C]ACTAAAATGGACAAG | 9886 |
rs12775287 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880262 | gagagagagtgagag[A/T]cagagagagagagag | 9886 |
rs12775465 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880241 | agagagagagagaga[C/G]agagtgagagagagt | 9886 |
rs12775476 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880263 | agagagagtgagaga[C/G]agagagagagagaga | 9886 |
rs12775625 | snp | C/G | 0.0803491 | 0.183626 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880179 | TACTGAGGGATGACT[C/G]TGTGTGTGTGTGTGT | 9886 |
rs12776441 | snp | G/T | 0.4776 | 0.103433 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920857 | gatgggggtctcact[G/T]tgctatccagggtgg | 9886 |
rs12776985 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880256 | cagagtgagagagag[A/T]gagagacagagagag | 9886 |
rs12778058 | snp | C/T | 0.499234 | 0.0195537 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995035 | GGCTTGGAAAATGGT[C/T]TAAACAACCCTGGCT | 9886 |
rs12778327 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933428 | AAAGATTTCATTTAA[A/C]GAATGTTCATTggct | 9886 |
rs12778430 | snp | C/T | 0.00938946 | 0.0678717 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880916 | CTGTGTGTAGGAACA[C/T]GTAACATTTCATTTC | 9886 |
rs12780009 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904059 | ccaccacctcccaca[C/T]tcaggtgattctccc | 9886 |
rs12780634 | snp | A/G | 0.479744 | 0.0985793 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981280 | CCAGAATTACTTTAG[A/G]GTCAAAATAATAAAG | 9886 |
rs16915675 | snp | G/T | 0.426354 | 0.177198 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887548 | TAACAATTATGAAAG[G/T]GTGCTGCGGGCAGCA | 9886 |
rs16915679 | snp | A/G | 0.250732 | 0.249999 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890372 | CAACTATGACCTGGC[A/G]GCAGTTCTGTTTTAA | 9886 |
rs16915682 | snp | A/G | 0.432063 | 0.171327 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891201 | AAACATACCTAGAAC[A/G]TCAGAAATTGTCTAA | 9886 |
rs16915734 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957640 | AAAGTGCTAAAAAGC[A/G]GATCCAAGTGAGTAA | 9886 |
rs17260420 | snp | C/T | 0.482234 | 0.0925596 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954991 | AGGGAAATAGTCCAC[C/T]TTGAGCTACCCATAC | 9886 |
rs17853098 | snp | A/G | | | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888753 | GGCTCCTTCACTCCC[A/G]TTTGGGGATTCTTCA | 9886 |
rs28423691 | snp | A/C | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946192 | CAGAAAAAAAAAAAA[A/C]AAAAAACTGACTTCC | 9886 |
rs28688850 | snp | A/C | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946191 | TCAGAAAAAAAAAAA[A/C]CAAAAAACTGACTTC | 9886 |
rs34003088 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920150 | ACCTGCTGAAATTTT[-/C]CTCACTAAGGCAGTC | 9886 |
rs34012455 | in-del | -/TTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955044 | TCTTTTCTTTCTTTC[-/TTTT]TTTTTTTTTTTTTTT | 9886 |
rs34046345 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958661 | ATGCTGGAGTACAGA[-/G]GGCATGATCACAGTT | 9886 |
rs34052498 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870298 | ATTTCCTAGACTCTT[-/G]GGAATTAGATTCCTT | 9886 |
rs34054281 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942720 | CCAAATTTCTAAACA[-/G]GGGTTTGTAAACAAA | 9886 |
rs34063925 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897971 | GCTTTGCAAAGAGCT[-/G]GGGATTACAGGCATG | 9886 |
rs34082747 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894212 | ATGCAGAAAACTGCA[-/G]GGTGCTTACATTAAA | 9886 |
rs34098194 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936001 | TAAGAAAATAATTTA[A/C]CAGTGTTAATAATGG | 9886 |
rs34153627 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897269 | AACCAGAAGCTCAAC[-/T]TTTTTTTCCAATCTG | 9886 |
rs34154360 | in-del | -/T/TAT/TATA | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986431 | ATATATATATATATA[-/T/TAT/TATA]AAATATATATAGGCC | 9886 |
rs34180214 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949045 | GGGCTCCAGCTAGTG[-/T]ATGACAAACAGGAAA | 9886 |
rs34211045 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879107 | GAAATGGAGGTTCAA[-/G]GGAGGTTAATTTAAA | 9886 |
rs34216593 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878848 | TGGGCATGGATTAAT[-/G]GGAGATGTACACTGC | 9886 |
rs34228057 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986831 | ACCTTAAATACAAAA[-/C]CCAATAACTCCCAAT | 9886 |
rs34241050 | multinucleotide-polymorphism | AG/CC | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956960 | TTACAGCTTGAAAAA[AG/CC]AACATATCGCTGTCT | 9886 |
rs34273804 | snp | G/T | 0.0995161 | 0.199636 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980655 | ACATACGAATGATGG[G/T]AACACACATAAAAAG | 9886 |
rs34290477 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930087 | CAACCCTTGGAAATT[A/C]AGAAAATACTTTCTA | 9886 |
rs34423754 | in-del | -/C | | | frameshift-variant, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910971 | CTTCATCAACAACAT[-/C]CCCGAGAACGCTCCA | 9886 |
rs34443719 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933885 | AATTAAAAGAGATTT[-/A]AAAAATTTACAGAAT | 9886 |
rs34486923 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905323 | GGTGTGGTGGTGGGC[A/C]CCTGTAATCCTAGCT | 9886 |
rs34517890 | in-del | -/T | 0.473174 | 0.112665 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991431 | GCCTTCCCTCAGTAC[-/T]TTTTTTTTTTTTTTT | 9886 |
rs34618721 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964388 | AAAGTCTCTCAAGCC[-/A]AAAATTTGAGACCTT | 9886 |
rs34658371 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920063 | TCTACAAATACACCA[-/G]GGAACCTCTCCTTTG | 9886 |
rs34666655 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978980 | AACACTGCCAAATCT[-/C]CCCCCTATGTATCAT | 9886 |
rs34669559 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882044 | CATGGCTGATTTTTT[-/A]AAAAAAGCCCGTTTC | 9886 |
rs34677336 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952727 | TAATGGGCTACAGCT[A/C]ATCTTAAATTCTGAT | 9886 |
rs34693835 | in-del | -/G | 0.426966 | 0.176587 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886728 | ATGTGGGGGGGGGGT[-/G]GGTCTGGCTATGTTG | 9886 |
rs34801893 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900462 | CTGCTTCCCTGTTCC[-/G]GGGAACTGACACCTC | 9886 |
rs34808058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986386 | GCTTTCCAAGAAATT[A/C]ATGAAATATAAATAA | 9886 |
rs34881079 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937056 | ACTTGGATTATTACT[-/A]AAAAAGGAAGAACAG | 9886 |
rs34920987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966470 | AGACCAGGAGTTTGA[G/T]ATCAGCTTGGGCAAC | 9886 |
rs34944534 | in-del | -/T | 0.231775 | 0.249335 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896979 | AAACAAAAAAAAGCA[-/T]TTTTTTTCAGTTATC | 9886 |
rs35083675 | in-del | -/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875819 | AGCTGAATTTACGTT[-/G]CTGGTCTGAAGCTAG | 9886 |
rs35122565 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970961 | CACCATTTTTATTTC[-/G]GGTAAAACTTCAGAG | 9886 |
rs35150002 | in-del | -/C | | | utr-variant-5-prime, intron-variant, frameshift-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944205 | GGCGAGAGGGGCTCG[-/C]CCCTTTCCACCCGCA | 9886 |
rs35173787 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951218 | GATACCACTTCAAAA[-/G]GGAATACAAGTGCTT | 9886 |
rs35179527 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964363 | CTAGGGGACACATGG[-/G]AAAATAAGCAAAGTC | 9886 |
rs35204781 | in-del | -/CC/CCA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881015 | ATAGCTCCCATAATT[-/CC/CCA]CACGTGTTGTGGGAG | 9886 |
rs35233304 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877901 | GCCCTGAGTCATCAT[-/C]CCTTACCTGCAAGTG | 9886 |
rs35255236 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960663 | TGCTTTCTTATTTAT[-/G]GGGAGATCATAATCC | 9886 |
rs35263444 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969569 | TCTGGGACCAGTAAA[-/G]GGGAATTTATAGAGA | 9886 |
rs35273919 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973881 | GTGATACAATTTTAT[-/C]CTTTGACGATGATCT | 9886 |
rs35314358 | snp | A/T | 0.426354 | 0.177198 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888029 | AAATGGAGACAATCA[A/T]ATTTAACCTTTAAGT | 9886 |
rs35359388 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897605 | CAGAAAGCTATGAGT[-/G]GGGACAGCCAAATGC | 9886 |
rs35393901 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932209 | GCAGACGTCTACACA[-/T]TTTTCAGTGACAAGG | 9886 |
rs35397648 | in-del | -/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876635 | AAAGTAATTGCCCAT[-/G]GGAAGCCTCCCAGAG | 9886 |
rs35399605 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890435 | AGTCCATACCCTTTA[-/G]GCTGGCACACAAGGC | 9886 |
rs35405188 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993162 | AGAAAATGGAGAAAA[-/C]CCCATTGTCTTCATT | 9886 |
rs35410411 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896704 | AATGTTTATATCTTA[G/T]GGAAAAATGACTTCT | 9886 |
rs35414815 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980347 | GGTAAGTTGAACACA[-/T]TTTTGACTAAGGTTA | 9886 |
rs35430567 | in-del | -/AA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882215 | TCTTAAAAAAAAAAA[-/AA]GAGTGATCAAAGAGA | 9886 |
rs35458475 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963028 | TAATACAGACCACGG[-/C]CTACAGATGTGATGG | 9886 |
rs35489242 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980514 | TTCTCAGGTACCTTT[-/C]CAGTCCTTTGCTTAT | 9886 |
rs35503016 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916604 | AGGTCCCTTTTGAAT[-/G]GGATGATCTTTTCCA | 9886 |
rs35508992 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918021 | ATTAACAAATCATGG[-/G]AATGGTAGCTTGTGA | 9886 |
rs35534540 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937083 | CAGGTACAAGTATTT[-/A]AAAAAAAATATCAAA | 9886 |
rs35538782 | in-del | -/A | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905449 | GAGAGACTCTTTCTC[-/A]AAAAAAAAAAAAAAA | 9886 |
rs35544473 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958051 | ACAGTTAATCTCATT[-/A]AAAAGCCAGTAATTG | 9886 |
rs35547680 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976810 | AGTACTTTTTGGTTT[-/C]CAAAAATACATGTTA | 9886 |
rs35559497 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961458 | CACCATTGTGAATAT[-/G]TTTACATGAACATAT | 9886 |
rs35572813 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986433 | ATATATATATATAAA[-/T]ATATATATAGGCCAT | 9886 |
rs35575286 | in-del | -/A | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905150 | ATCCAGATAATACTT[-/A]AAAAAAAAAAAAAAT | 9886 |
rs35582414 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996578 | CAGCCTGGAACCCAA[-/G]GGGATGGTTATGCGA | 9886 |
rs35646647 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893242 | GATGCATTGACGTTT[-/C]CCGATGAAGTTATTT | 9886 |
rs35651083 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964338 | CCTGGGTTTTGGGCC[-/A]CCACTGCCCTCTAGG | 9886 |
rs35679478 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887992 | ACCTAACCTCTCTGT[-/G]CCCTTGGTTTCTCCA | 9886 |
rs35692448 | snp | G/T | 0.0109375 | 0.0731386 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886273 | ATGAGCCAACTTTGC[G/T]GAGAGCTTCAACCAA | 9886 |
rs35813234 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934089 | TGTGACATAAAGAAA[-/T]TTTACAAAAAAGAGG | 9886 |
rs35882975 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894260 | TCTTTAAATTTATAT[-/C]CCAAGAAAAGCTGCA | 9886 |
rs35901283 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893291 | CAAACTTGTCTCAGT[-/C]CCTGGAACCACAACA | 9886 |
rs35937161 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993897 | TTTTGGTGACATTTA[C/G]CTCAATAGTGCAATT | 9886 |
rs35965622 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892904 | CGGGTGTTCGAGGGC[-/A]AAAGTGCTTGATTTC | 9886 |
rs41274044 | snp | C/T | 0.10237 | 0.201756 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877223 | TGAAGTTAAGCCAAG[C/T]TTCCCTTTTTTCTCT | 9886 |
rs41274046 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877408 | TAGCCCCATTTTAAA[A/G]AGCGAGAAAGCTGAG | 9886 |
rs41283538 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870317 | ATTAGATTCCTTTCC[A/G]TGTAGGAGAACGCAG | 9886 |
rs41283540 | snp | C/T | 0.02016 | 0.0983543 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871385 | AAACCTGAACTATGT[C/T]GTATCTCTAACAAGA | 9886 |
rs41283542 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871708 | TGATGCCTTTTATGT[A/G]CTAGGCCTTGAGCTT | 9886 |
rs55693439 | in-del | -/CTGT/CTGTGTGT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880178 | TACTGAGGGATGACT[-/CTGT/CTGTGTGT]GTGTGTGTGTGTGTG | 9886 |
rs55738621 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988033 | GTGCCTCCTGGGTAC[C/G]CCATTCTCCTGCCTC | 9886 |
rs56057124 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893538 | ATGTAGACAGCATAG[C/T]CACTTATCTGTTTCC | 9886 |
rs56057594 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909943 | ATGACAATAAAAGTC[C/T]GTTCAAAGAGCTACT | 9886 |
rs56304838 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966688 | TTCTTTTTTTTTAAT[A/C]TTTATTTTTTTTACT | 9886 |
rs56773667 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919340 | ATTGACAGGAAAAAA[A/G]GAAAATGTTAAAAGT | 9886 |
rs57003615 | snp | C/T | 0.119281 | 0.213102 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920746 | CCCCTACCTCCACCT[C/T]TCGGCTCAGGCCATC | 9886 |
rs57200979 | in-del | -/CA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997105 | ACACACACACACACA[-/CA]GCTTTTGCTACAATG | 9886 |
rs57390948 | snp | C/T | 0.11228 | 0.208646 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982504 | ATTTTGTTGGCCAGA[C/T]GACTCTGTTGTTGGG | 9886 |
rs57517818 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900939 | ATAATTTCATAACAT[C/G]AGAATAATAATGCAT | 9886 |
rs57527631 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905800 | CTATGAACATTAAGA[A/G]CTAACTCAAAATGCT | 9886 |
rs57642119 | in-del | -/C | 0.477768 | 0.103061 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919335 | TATTATTGACAGGAA[-/C]AAAAGGAAAATGTTA | 9886 |
rs57689486 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973460 | TTCTTTTTTGTTGTT[A/G]TTTTTAATTAGCACT | 9886 |
rs57915354 | in-del | -/G | 0.488545 | 0.074807 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985233 | TTATGGGTGGACAAA[-/G]GAGAGTAAACTGTCC | 9886 |
rs57963914 | in-del | -/GGCCCCTGGGTCAGACTATG | 0.499137 | 0.0207489 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903681 | CTGGGTCAGACTATG[-/GGCCCCTGGGTCAGACTATG]AGCCACTGAGGCAGG | 9886 |
rs57968713 | snp | C/T | 0.115788 | 0.21092 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935437 | GAAAACTTTTTGTTA[C/T]ATACTGATAATTTTT | 9886 |
rs58126188 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920638 | TTTTTTTTTTTTTTA[A/T]GTTTTGTTTTGTTTT | 9886 |
rs58366875 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940804 | ATATGGAATTGCAAA[A/G]TAATTCCACAGAGTG | 9886 |
rs58678854 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935571 | TCAGTGTAAAGCAAG[A/G]TTGGGAATCACTACA | 9886 |
rs58723098 | in-del | -/TTTTA | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990506 | AGCAATTTCTCTTTA[-/TTTTA]ATTCAAAAATAATTC | 9886 |
rs58729805 | snp | C/G | 0.101301 | 0.200969 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945952 | TGGGAGGCCGAGGCG[C/G]GCGGATCACGAGGTC | 9886 |
rs58771689 | in-del | -/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961812 | TATAACCTTTTTTTG[-/T]TTTTTTTTTTTTTTG | 9886 |
rs58848291 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886728 | ATGTGGGGGGGGGTG[-/T]GGTCTGGCTATGTTG | 9886 |
rs58871616 | snp | A/G | 0.101301 | 0.200969 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946331 | TCAGTCCTCTTCATT[A/G]CAAGCTATTTCTCAT | 9886 |
rs58881527 | snp | C/T | 0.11963 | 0.213316 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920032 | TGCTGGGTTCAGACA[C/T]ATGGGTCTACTTTCT | 9886 |
rs58964987 | snp | C/T | 0.181978 | 0.240568 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001963 | CTTTTCTTATAGGGA[C/T]GTTCTCTAGCCAACT | 9886 |
rs59082796 | in-del | -/A | 0.481703 | 0.0938806 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928331 | GTATATATCCAAAAC[-/A]AAAAAAAAAAGAAAA | 9886 |
rs59145772 | snp | A/C | 0.101301 | 0.200969 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002931 | TTTCTTCTTCTTCTT[A/C]TTATTATTATTATAA | 9886 |
rs59513557 | snp | A/C | 0.120326 | 0.21374 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931776 | TCTCACATAAAAAAA[A/C]CCCCACAGGAATCAA | 9886 |
rs59849939 | snp | A/G | 0.138886 | 0.22395 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873533 | TGTGTATGGGGGTAA[A/G]GTGGGAACACAGTGC | 9886 |
rs59969318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934358 | CCTTTACTTATATCA[A/T]AGGAACTAATACCTC | 9886 |
rs59979291 | snp | A/C | 0.193028 | 0.243422 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002934 | CTTCTTCTTCTTCTT[A/C]TTATTATTATAATAC | 9886 |
rs60136105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000109 | TTTTAGACTCAGGAA[C/G]CATTTTACAAATCTT | 9886 |
rs60136964 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931621 | TAAGTATAACCCTTG[A/T]TTTTCACTTCTAAGA | 9886 |
rs60439820 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920637 | TTTTTTTTTTTTTTT[A/T]AGTTTTGTTTTGTTT | 9886 |
rs60447404 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915155 | TTCATTTGTTACACA[C/T]AAAGAAACATTAAAT | 9886 |
rs60499252 | snp | A/G | 0.0626037 | 0.165477 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869805 | ATGGATGCATTTGTA[A/G]CTATCCCTACTCTAC | 9886 |
rs60679581 | snp | A/C/G/T | 0.00358891 | 0.0422285 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969245 | TGCAGATACAGGGTG[A/C/G/T]GGCACATATGACTTG | 9886 |
rs60706061 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972423 | ATCATTCTCAGCAAA[-/A]CTAACACAGGAACAG | 9886 |
rs60921763 | in-del | -/A | 0.46865 | 0.121211 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895400 | GTTAAAAATAAGATT[-/A]TTTTTTATTTATTTA | 9886 |
rs60928572 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915321 | TTTATTTACGTAGAA[C/T]GAGAGTAATAAGTAT | 9886 |
rs61304036 | in-del | -/G | 0.122411 | 0.214991 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920148 | TCACCTGCTGAAATT[-/G]TTCTCACTAAGGCAG | 9886 |
rs61606206 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908280 | CCGAAGGCAAGGTCT[A/G]AAACATGTTGGTTTA | 9886 |
rs61631054 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908933 | ATGTTGCTCAGAGAA[A/T]CAAACTTGGCTTGGG | 9886 |
rs61754071 | snp | A/G | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888601 | GCTTCCAGCCCCAGA[A/G]CCTCCACCAGGCTCT | 9886 |
rs61759908 | snp | C/T | 0.00199421 | 0.031514 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877966 | GGCAATTAATTCCAG[C/T]GGGTCCAGATCCAAG | 9886 |
rs61853063 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932083 | AAGAAGAAAGTAGTT[C/T]CAGATTTGTTGGTAT | 9886 |
rs61853064 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939619 | GGTGGGAAGCCTGGC[A/T]GAGAAGAAAAGAGGA | 9886 |
rs61853065 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951835 | GCCAAGGCGGGCAGA[C/T]TGCCTGAGGTCAGGA | 9886 |
rs61853066 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962301 | CCAATATAACTCTTC[C/T]CAACAGAAAAAGAGA | 9886 |
rs61853068 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977940 | TCATTTACCCGTTAA[C/T]TGATATGCACAGGAA | 9886 |
rs61853326 | snp | A/G | 0.128288 | 0.218372 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871352 | AAATGCACAAAAGTG[A/G]AGGAAGATCAGTGCC | 9886 |
rs61853327 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872598 | TCTAGTGCTAAACAA[A/C]CGTGGCCTCTGGAAG | 9886 |
rs61853328 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881264 | CTTTATAAATTACCC[A/T]ATCTCTGGTATGTCT | 9886 |
rs61853329 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881265 | TTTATAAATTACCCT[A/G]TCTCTGGTATGTCTT | 9886 |
rs61853331 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905167 | AAAAAAAAAAAAATT[A/C]AGGCTGGGCATGGTA | 9886 |
rs61853332 | snp | A/G | 0.203267 | 0.245593 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914861 | AATCCCTAGCAGTCC[A/G]CTCCAGACCAAAGTG | 9886 |
rs62940062 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893106 | TCTCATGTCACAATT[A/T]AAAAAAAAAAAGACC | 9886 |
rs66585379 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986432 | TATATATATATATAA[-/T]AATATATATAGGCCA | 9886 |
rs66851123 | in-del | -/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920622 | TAGGTTCTGATTTGC[-/T]TTTTTTTTTTTTTTA | 9886 |
rs67395123 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919336 | ATTATTGACAGGAAA[-/C]AAAGGAAAATGTTAA | 9886 |
rs71018931 | in-del | -/GAGAGAGAGAGA | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880234 | AGAGAGAGAGAGAGA[-/GAGAGAGAGAGA]GAGAGACAGAGTGAG | 9886 |
rs71018933 | in-del | -/A | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905475 | AAAAAAAAAAAAAAA[-/A]TTCAAATTAAGGCAA | 9886 |
rs71018934 | in-del | -/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920966 | TTGTTTTTTTTTTTT[-/T]ATGAGACAGTGTCTC | 9886 |
rs71018937 | in-del | -/TTTT | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987948 | TTTTTTTTTTTTTTT[-/TTTT]AAGACCGAGTCTCGC | 9886 |
rs71468908 | in-del | -/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881053 | ATGGGAGATATTCAT[-/G]GGGGGTGGTTCCCCC | 9886 |
rs71468909 | in-del | -/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989791 | TCCCTCCACCCCTGC[-/T]TCTCTCCCCACACAG | 9886 |
rs71468910 | in-del | -/A | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989829 | GCAGGTGGGAGAGGC[-/A]AAGCCAGCACTGCTT | 9886 |
rs71468911 | in-del | -/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989842 | GCAAGCCAGCACTGC[-/T]TTCGTGACATTTATT | 9886 |
rs71468912 | in-del | -/C | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989859 | CGTGACATTTATTTA[-/C]CCCTGGCTGTAGGAG | 9886 |
rs71499294 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942282 | TGGCTTTTCCTGTTG[G/T]ATTTGTATAGCTTAT | 9886 |
rs71499295 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995052 | AAACAACCCTGGCTG[C/T]GTACATCAATACATT | 9886 |
rs72338375 | in-del | -/TAACTC | 0.490836 | 0.0670685 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953977 | GCTTTAAATTTACTT[-/TAACTC]TATTCCATGTTATTG | 9886 |
rs72811889 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876500 | TTGATCACAAACCTT[G/T]TTGGGCAGATTTGGC | 9886 |
rs72811890 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876757 | CAACTCGCTCTTTCT[A/G]TCTAACTGGGGAGGA | 9886 |
rs72811891 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887098 | AAAAAACAGAATCCA[A/G]TTGAGACTCCCACAT | 9886 |
rs72811893 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911877 | GGACAGCTGGCACAC[A/T]TTTATAGCCTACTGG | 9886 |
rs72811901 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951134 | TCATTTAATCTAACC[C/T]TGATCTTCTGACTAT | 9886 |
rs72813711 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970035 | CCAACTGGGTAAAAT[C/T]ATTACTCAAAGACTG | 9886 |
rs72813720 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993259 | ATTACAATAAGCCAT[A/G]AAACCTTAATTATAA | 9886 |
rs73263836 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914888 | AGTGACTGCCAAAGG[G/T]GCTGACCCTTGTGCA | 9886 |
rs73263839 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916813 | TTAGTCAGCCGACCT[C/T]AATATAAGCAGATTA | 9886 |
rs73263841 | snp | A/C/T | 0.00993785 | 0.0698258 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916854 | TCTATGTGGGTGCAA[A/C/T]GCAATCACGATGGTC | 9886 |
rs73263902 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917633 | AATCTCATCATGGGG[A/C]TCCACCCTCATGGCT | 9886 |
rs73266003 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918547 | GTAGGGCCACTAATT[G/T]ATTTCAGGCAAGCGT | 9886 |
rs73266013 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924482 | AACACTCGAGCATCC[A/G]GATATATAAGGCAAA | 9886 |
rs73266015 | snp | A/G | 0.116488 | 0.211364 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925043 | GAACTCTTGCTCTCA[A/G]TTCACACAAGATCTG | 9886 |
rs73266017 | snp | C/T | 0.122064 | 0.214785 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925332 | ATGCTCCTGAATGAA[C/T]GTTGAGTCATTGAAG | 9886 |
rs73266019 | snp | A/G | 0.11963 | 0.213316 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926264 | AAATAAATATGGACA[A/G]GACCTGATGGCTTCA | 9886 |
rs73266021 | snp | A/G | 0.118235 | 0.212457 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930309 | TATCTCCTTCCACGG[A/G]TTGTTGTGAAGATTA | 9886 |
rs73266023 | snp | G/T | 0.117886 | 0.21224 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932599 | TGGGGGTGGGGCACA[G/T]CTAAGGGCTGGATCG | 9886 |
rs73266025 | snp | A/G | 0.115788 | 0.21092 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933202 | GCTAGTATTTTTCAG[A/G]GCATGTTCCTATACC | 9886 |
rs73266026 | snp | G/T | 0.120326 | 0.21374 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933954 | AAAGAGATTGAGATA[G/T]AGATATACTAAAATA | 9886 |
rs73266028 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934496 | CTAATCTTTCCAGAT[C/G]AAGACATGAGACTTT | 9886 |
rs73266031 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934697 | AGCTGCCAAATTTAG[A/C]CTTTGGCTCCATGTC | 9886 |
rs73266037 | snp | C/T | 0.122064 | 0.214785 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941542 | CAACCACGGGCACCA[C/T]TCTGATGCCTAAAGT | 9886 |
rs73266038 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942251 | ATATAATCATAATTA[A/G]AAGACCAAACAATTT | 9886 |
rs73266041 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943109 | ATTTTTGCCCCCAGC[A/G]ATTGTGTACAGTCAG | 9886 |
rs73266043 | snp | A/T | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945188 | CAGTCAGCCTGCTAA[A/T]ATTAGTATGCCTTAT | 9886 |
rs73266049 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947397 | TATCAAAGTCATAGG[A/G]TTAAAAAAAATCCCA | 9886 |
rs73266051 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947515 | ATCTGTTCTCCATCT[C/G]TAGAGTTTTTTTATT | 9886 |
rs73266054 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947721 | GAGTTTGTTTATCCA[C/T]TCACCCACTGAAGGA | 9886 |
rs73266056 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948428 | AAGAAACAGGGAGAC[C/T]TTAGCCACGTGTAGT | 9886 |
rs73266059 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948819 | AACTTTCTGGCTTCC[C/T]AAAGAGGAAGAGGCT | 9886 |
rs73266064 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949823 | TTCATTGTTAGTTCT[A/G]TGAAGACAAAGTATC | 9886 |
rs73266066 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950648 | AATAACTTTCCAAAA[A/C]GTCCTTAAGGTGACT | 9886 |
rs73266068 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950673 | GTGACTAAATGAAAT[A/G]ATGTTTGTGGAAAAT | 9886 |
rs73266070 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950922 | AAGTTTAGTATTTGA[A/G]GTTTGAATGTTTTGC | 9886 |
rs73266072 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952058 | GCGAGACTCTGTCAC[A/C]GCCCCCCACCCCCCC | 9886 |
rs73266076 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952092 | AAAGAACGGTACATG[A/T]TAAAACTTTTATAAG | 9886 |
rs73266077 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952297 | AAAATGTTTCACAAA[G/T]ATTACAGTGTCATAA | 9886 |
rs73266078 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952444 | AGCCAAATGCTTTTA[C/T]ACTCACTTTCATTAA | 9886 |
rs73266084 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957653 | GCAGATCCAAGTGAG[A/T]AAGTAGTGGTAAAAG | 9886 |
rs73266086 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957997 | CTTACTGTGAGCAGA[C/T]ACCACTTGTGAGTGT | 9886 |
rs73266087 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958343 | ACTTCTGAGCCAACC[A/G]TCTTGCAAAAGGAAC | 9886 |
rs73266088 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958968 | CATCTTCATTTTGGT[A/T]AACTATTACTTTGGT | 9886 |
rs73266091 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961180 | AGGCACTGTGGCATG[C/T]CATGCAAATTACACT | 9886 |
rs73266094 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964927 | GCAGAAATTAATCTG[C/T]TCTTTCATTCCTAAA | 9886 |
rs73266095 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969594 | TAGAGAGACAGATTA[C/T]GGCTCAATTAGGATT | 9886 |
rs73266096 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970484 | TCAGATCGGTATTGA[A/T]TATTAATTCTGTATT | 9886 |
rs73266102 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975538 | GCTACTTATTCGCTT[G/T]CATGGAAATACTAGG | 9886 |
rs73268005 | snp | A/T | 0.046775 | 0.145601 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978504 | AGGCTAAGTTGGGAG[A/T]GAGAGTGGGTATGTT | 9886 |
rs73268006 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978511 | GTTGGGAGAGAGAGT[A/G]GGTATGTTGGGTCTC | 9886 |
rs73268008 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982891 | TTGCCCTCTTTCCTC[G/T]TCCGCTCCCTTCTTA | 9886 |
rs73268011 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982953 | GGTGCACATGACATA[A/G]GGCACAGAACTTTTA | 9886 |
rs73268015 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983974 | ATTTTTATCACTTAC[A/G]TACTTTAATTCCCAA | 9886 |
rs73268016 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986221 | CTTCCTGGTGATGCT[G/T]CCCTCATCTTCCAGG | 9886 |
rs73268017 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987608 | CCTCTCATCTAATGT[A/G]TTCCTGCTTCCAATC | 9886 |
rs73268018 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988555 | AGTGAGAATATACAG[G/T]ATTTGGTTTACCAGT | 9886 |
rs73268024 | snp | A/G | 0.029116 | 0.117091 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990640 | CCTCTGCCCCCCATG[A/G]CCCAGGAATCCCTGC | 9886 |
rs73268034 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998628 | ACGGGAAGGAAGGGG[A/G]TGGAAAAAGGGGAAG | 9886 |
rs73268035 | snp | A/G | 0.146314 | 0.227484 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998753 | AATCCAAAGCTAGTG[A/G]AAGGAAACCAGAGGC | 9886 |
rs73280532 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879340 | TATGAGCTTCTTTTT[A/C]TTTCTTTTTTATTTT | 9886 |
rs74155406 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889928 | CTTCATCACCTTCAC[C/T]TTTATCAACAGCATC | 9886 |
rs74155409 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905856 | TACTTTTTTGCTTGC[C/T]GTAAAACACAAGCAC | 9886 |
rs74155411 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906484 | CATCATCATCACAAA[C/T]TACAACAGCATGGTG | 9886 |
rs74155412 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914652 | CAAATAAGCTGAATC[A/T]TAGCAGCACTGACGG | 9886 |
rs74155413 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937748 | AAGAAAAAAAGGTTC[C/T]TATAACCATTCCTTA | 9886 |
rs74155415 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940707 | TTGGGTTGAAATTCT[A/G]CATTCTGTCCTTTCC | 9886 |
rs74155420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965510 | CTAGCATGGTGCCTG[A/G]CATGTAGTAGGTGTT | 9886 |
rs74155428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983877 | CTTCTTCCATCTCCT[A/G]ATTTCAGTATCTTTT | 9886 |
rs74155430 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986760 | GCTTGGAGGTAGTTA[C/T]TATTGCTGTAAAAAC | 9886 |
rs74155434 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995533 | GGAACAACATTCACA[C/T]GCTGATTAATTTAAA | 9886 |
rs74155436 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995678 | AAATAATAAAGGGTT[A/G]AATGTACTTATTTAA | 9886 |
rs74155437 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996389 | TGTCTTCCCACCCAC[A/C]ATCCAGCTAAATTCT | 9886 |
rs74155438 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998072 | ATTCTGAGCTTCAGT[G/T]TCCTCTGCCGTAAAA | 9886 |
rs74157866 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875489 | GCAGAAAGTTCTACT[A/G]GATGGAGTGGCTCTA | 9886 |
rs74157867 | snp | A/G | 0.0770498 | 0.180522 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876634 | AAAAAGTAATTGCCC[A/G]TGGAAGCCTCCCAGA | 9886 |
rs74157868 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880775 | ACATATGAATAATTA[A/C]TTATTCAACTAAATC | 9886 |
rs74388070 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925578 | AGAATTAATAAAGAT[C/T]GGAGCAGAAATAAAT | 9886 |
rs74394771 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877317 | ACATAATGCTTACTA[C/T]GTGCCAGACGCTGTT | 9886 |
rs74411406 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937072 | AAAAAGGAAGAACAG[C/G]TACAAGTATTTAAAA | 9886 |
rs74416154 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893116 | CAATTAAAAAAAAAA[A/G]AGACCAGATATTAAA | 9886 |
rs74439597 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920023 | TGAACTGTGTGCTGG[A/G]TTCAGACACATGGGT | 9886 |
rs74452887 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940190 | CTTCACTAATTAAGA[C/T]TTTAGAGCTATTAGC | 9886 |
rs74470531 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929875 | GCTAAATTAATAAAT[A/T]TCCCACATTTTTTAA | 9886 |
rs74490355 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876470 | TATTTAAGCAAAACT[A/G]GTACTAGTCTGAGAT | 9886 |
rs74556819 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990899 | GTCTGCTGTCTCCCG[C/T]GATGTCTCAAGACAT | 9886 |
rs74575666 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904438 | CCCTCCCCTCCATCC[C/T]CTTCTCTAGGAAACC | 9886 |
rs74577734 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920623 | AGGTTCTGATTTGCT[C/T]TTTTTTTTTTTTTAA | 9886 |
rs74595600 | in-del | -/AA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934972 | TATAGAGAAGGCAGT[-/AA]CGAGATTGGCTGCTC | 9886 |
rs74616145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913607 | TGCAGTGTCTGGAAA[C/T]GTGTCTGGTTGTCAC | 9886 |
rs74793386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985158 | TTTAAATATGCATTA[A/G]AACATATAAACATAT | 9886 |
rs74796329 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994316 | TATACTACAATAAAT[A/G]AAACAAAGTGATGTA | 9886 |
rs74804040 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885299 | AACTATGTATAATAA[C/T]TATTATTTGTCAGTT | 9886 |
rs74832048 | snp | C/G/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884625 | TAAGAAAATGTGGTA[C/G/T]TTATACACAATGGGA | 9886 |
rs74837606 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941573 | GAAAAATAAAAAGTC[A/G]TATGATGGACAAACT | 9886 |
rs74860329 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904885 | TAGTTCTTTTTGTTA[C/T]AGCAGCACACTGAAC | 9886 |
rs74868809 | snp | C/G | 0.11228 | 0.208646 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978507 | CTAAGTTGGGAGAGA[C/G]AGTGGGTATGTTGGG | 9886 |
rs74877615 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910315 | CCCATTACTAGATTT[G/T]TTTCTCCTTTTTAAA | 9886 |
rs74963121 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951653 | TCACGGTATCCATCT[C/T]AGAAGAGCTTGAAGA | 9886 |
rs74993470 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988496 | AGTGTCTGTTGTTCC[A/C]TTCTTTATGTCCATG | 9886 |
rs75033476 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878442 | AGCTGCAAACCACAC[C/T]GTTGCTGACATGATG | 9886 |
rs75049046 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941295 | CTCTAAACTTCCAAC[C/T]CCTCACCTATAGTTT | 9886 |
rs75052198 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954327 | ATTACACTCTTCATG[C/T]TGAAATTATTATAAA | 9886 |
rs75063473 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932512 | CAATACTTTCTTAAA[A/G]TAAAAAAAAAAAAAA | 9886 |
rs75072181 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922162 | AATTCAAGGGATTCT[C/G]AGCGCTTTTTGGTGA | 9886 |
rs75193454 | snp | A/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927716 | ACAAAAATTAAATCA[A/G]AATAGATTAAATACT | 9886 |
rs75201428 | snp | A/C | 0.030278 | 0.119257 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885112 | GGTGTTCTATTGCAC[A/C]GTATGGTGACTATGG | 9886 |
rs75273490 | snp | A/G | 0.00358779 | 0.0422022 | nc-transcript-variant, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000960 | AGAAGACCCCAGTGT[A/G]GCACGTCCAGCCCAG | 9886 |
rs75291391 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910019 | CAAGGAGTAATTCAC[A/G]TGCTTGGAGTACCTA | 9886 |
rs75308921 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890334 | ACAGTCCTCACTGCT[G/T]CAAGAAAAGTCTTTA | 9886 |
rs75333550 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878678 | CAAAGGACTCCTTGC[C/T]TGGGACTTCCAGGGG | 9886 |
rs75411013 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954146 | TGAGAATATAGACCA[C/T]TGGCTTGAAAGTAGA | 9886 |
rs75550065 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900912 | AAAAATCTCTTTACC[C/G]CATGTAATTGGATAA | 9886 |
rs75557547 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962902 | CCACTTAAAATATCT[A/G]CCAGTTTCAATGTAT | 9886 |
rs75565631 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896553 | GAAAAGGGGTAGGAA[A/G]GAGTTTGGAATGTTT | 9886 |
rs75565632 | snp | A/G/T | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949379 | AGAATCTGTGTGTTC[A/G/T]TAGTTTTTGCACTTG | 9886 |
rs75595562 | snp | G/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961824 | TTGTTTTTTTTTTTT[G/T]TTGAGACAGAGTTTC | 9886 |
rs75611311 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970226 | TATTTGTGGTTACAA[A/G]TCTATTCCAATTTTG | 9886 |
rs75636795 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968699 | TTTGAGACTGACAGC[C/T]GGGCACCAAATGATT | 9886 |
rs75642734 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992138 | TTAAATCCTGGGGTA[C/T]ATTTTGCACAGAACT | 9886 |
rs75653192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907597 | AGAGCGTTACAACAC[C/T]CATGCTACTCTGTTT | 9886 |
rs75806875 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958195 | TGAACCCATTTTTAT[A/C]TGCATAAGGTTGAAG | 9886 |
rs75824772 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884935 | TTGTCCTTTTTTTTT[A/T]AGAGACAGGTTCTCA | 9886 |
rs75835580 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908972 | TCCTGTTTCTATCAA[A/C]GGGATAATGGGTTAC | 9886 |
rs75847967 | snp | G/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961811 | TTATAACCTTTTTTT[G/T]TTTTTTTTTTTTTTT | 9886 |
rs75857810 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929991 | CCAAAGTGTAAATTG[C/T]TGTCAACCAAATTCT | 9886 |
rs75873005 | snp | C/T | 0.093777 | 0.195178 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921462 | GACACACTGCAAACA[C/T]CCTTCCTTTACACTG | 9886 |
rs75948496 | snp | C/G | 0.0944967 | 0.195752 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915838 | CACACAGCGTTCTTG[C/G]GCCTACAGGATGGTG | 9886 |
rs76042637 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924272 | GACACTATTTGAAGA[C/T]GATTTTAAAAACATG | 9886 |
rs76057350 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949467 | TTGGGAATTATCTCA[A/G]GTATTACTCAGACCA | 9886 |
rs76099320 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984545 | TAATTAACTGAAAAC[C/G]CATAAGACAGAACTT | 9886 |
rs76108778 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948783 | CTTGCAGTTAAGCCA[G/T]TGGCTTTAATAACAC | 9886 |
rs76121616 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923904 | GTCCATGAAACCTCA[G/T]TTTCTCTATAAATTA | 9886 |
rs76141848 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939293 | ATCCATCATTTTTGG[C/T]GTCTTTTTGCCAATT | 9886 |
rs76149888 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906909 | TCGAATCGTAGCTCC[C/T]GTGATTCTCACATGT | 9886 |
rs76187307 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896999 | TTTCAGTTATCTTTC[A/G]AGGGGAACACTGGCC | 9886 |
rs76298424 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885764 | TACTTGGTTTTGATA[A/G]TACCATGCCTGGTGA | 9886 |
rs76302988 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919239 | TTAAGAAGTAATTTA[C/G]CTCAGCCATTAAAAA | 9886 |
rs76366775 | snp | G/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961825 | TGTTTTTTTTTTTTT[G/T]TGAGACAGAGTTTCC | 9886 |
rs76442845 | snp | A/C | 0.0217823 | 0.102488 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953104 | AATGGGAAAGTCATG[A/C]GGAAAAACACACAGC | 9886 |
rs76458517 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888159 | CATGTCTGGCTAACG[C/T]TCAATGAAACACAAT | 9886 |
rs76481471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997848 | TTTCTGAAAGAAAGC[A/C]TCATTGTCCAAAGCT | 9886 |
rs76485641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961239 | TGAACATATAGGAAA[C/T]CTTGTATTCAGGAAG | 9886 |
rs76488904 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987241 | CCCTGAATTTTCTTC[G/T]TCTGGCTTCTCTTCT | 9886 |
rs76518535 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901151 | AAGCATAGTCAAGAT[A/G]ATACATTGAAAAAAG | 9886 |
rs76522289 | snp | C/T | 0.109461 | 0.206758 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872404 | CTTATATAACTAATT[C/T]GGTAAACCTCTTGTT | 9886 |
rs76526069 | snp | A/T | 0.122064 | 0.214785 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941223 | AGACAAAAACTTTTT[A/T]AAAAATCCTATTTGT | 9886 |
rs76541698 | snp | A/C | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928331 | GTATATATCCAAAAC[A/C]AAAAAAAAAAGAAAA | 9886 |
rs76645904 | snp | A/G | 0.00822899 | 0.0636143 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892775 | GTAAATTTTAACTTG[A/G]TCAGGACAGGGAAAC | 9886 |
rs76649613 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920002 | AGATTTCAAAACCAC[C/T]ATAAGTGAACTGTGT | 9886 |
rs76740386 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884937 | GTCCTTTTTTTTTTA[G/T]AGACAGGTTCTCACT | 9886 |
rs76747011 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996169 | CTATGATTTTTCTTA[A/T]TCTTTCCTTTAGTTT | 9886 |
rs76759711 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909940 | TAAATGACAATAAAA[C/G]TCCGTTCAAAGAGCT | 9886 |
rs76772759 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899296 | GGCTTGCTAAACAGA[C/T]GAAGGTGAAATTGTG | 9886 |
rs76858454 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909944 | TGACAATAAAAGTCC[A/G]TTCAAAGAGCTACTG | 9886 |
rs76892038 | snp | A/C | 0.031825 | 0.122064 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897517 | TAATTCTGACATTAT[A/C]TTTTTATCTAGAAGC | 9886 |
rs76937479 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939812 | CCATTTTTAAAGAGG[C/T]AAGTCATGCATACTA | 9886 |
rs76939362 | snp | A/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966507 | AGACCCTATCTCTAA[A/T]TAAAAAAAAAAAAAG | 9886 |
rs76965186 | in-del | -/A | 0.179744 | 0.239925 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887076 | GTATTTCATAGCTTT[-/A]AAAAAAAAAAAACAG | 9886 |
rs76966910 | snp | G/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913886 | TCATAAAAATACTCA[G/T]CTCCTAAGGTTGTTG | 9886 |
rs77013307 | snp | A/C | 0.029116 | 0.117091 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939244 | GGAGTGTCCTGGGAC[A/C]TCTGGAAAAAGTGGC | 9886 |
rs77025782 | snp | A/T | 0.0952156 | 0.196321 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940763 | TCCAGACAAAAAAAA[A/T]GTGCTTGGAAATTTT | 9886 |
rs77085210 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991449 | TTTTTTTTTTTTTTT[G/T]AGACAGAATCTTGCT | 9886 |
rs77121022 | snp | C/T | 0.137527 | 0.223271 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910058 | AATCCTGTAAGGTGA[C/T]ATGATGTTTGATGTT | 9886 |
rs77133633 | snp | C/T | 0.136506 | 0.222754 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891786 | AAAGAAACGTATTTC[C/T]CTCCACATGGTTTGG | 9886 |
rs77172899 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910312 | TTTCCCATTACTAGA[A/T]TTTTTTCTCCTTTTT | 9886 |
rs77205222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896190 | TCCCATGTGGAGACT[C/G]TTCAATGTCTGACAT | 9886 |
rs77208962 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974343 | GAGATATAAATAGAC[A/G]TGAAAGACAACTATC | 9886 |
rs77218848 | snp | C/T | 0.0988009 | 0.199095 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942221 | TCATCCTATTCAAAA[C/T]AGCATTTTTAGACAA | 9886 |
rs77270060 | snp | A/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995857 | AAGATAAAAAAAAAA[A/T]TCAGGTTCAAGCAGG | 9886 |
rs77295690 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870407 | TGGTCTGCCTTAGCC[C/T]ACTTCTGCAGCAACA | 9886 |
rs77329134 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892437 | GTTCTCTGGGGCCCA[G/T]ATACCTCTAAGTGTT | 9886 |
rs77351808 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949641 | GTTATGACTGTTGGT[A/G]TTGATGTGGTTTCCA | 9886 |
rs77394867 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887934 | AGAGCATGGGTTCAA[A/G]TCCTGGCTCTACCAT | 9886 |
rs77406882 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920927 | CTCCCAAAATGCTGG[A/G]ATTACAGGACTGATT | 9886 |
rs77411608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909965 | AGAGCTACTGGCTTG[C/T]AGAAATAGAAGAATC | 9886 |
rs77424901 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924915 | CTTTTCCCTGACCCA[A/G]TCTCATGTTAAATTG | 9886 |
rs77482806 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995256 | AGGCACCTTACTGAG[G/T]ACTCAGTGCACATAC | 9886 |
rs77498605 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988533 | CAACATTTAGCTCCC[A/G]CTCATAAGTGAGAAT | 9886 |
rs77502434 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904629 | AGTATCAGAAAATTC[C/G]AGGACGGTGTTTACC | 9886 |
rs77608451 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940744 | CTCACCGATTAATCA[C/T]CTATCCAGACAAAAA | 9886 |
rs77701118 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931256 | GATATTAACAGGGTT[G/T]TGCAACCATTCCTGC | 9886 |
rs77734945 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961157 | TTGGTCTTCTGTTGA[A/T]GTTCAAGAGGCACTG | 9886 |
rs77745609 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993505 | ACTGATTTTTTTCTC[A/C]TTTGCATTGCCTGCT | 9886 |
rs77746474 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901152 | AGCATAGTCAAGATG[A/G]TACATTGAAAAAAGA | 9886 |
rs77746905 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988497 | GTGTCTGTTGTTCCA[A/T]TCTTTATGTCCATGT | 9886 |
rs77768398 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964944 | CTTTCATTCCTAAAG[A/T]CTTAAGGAAGAATTT | 9886 |
rs77775825 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872638 | CACAGCAGAAAGCAG[C/T]GATGTCATCTCTGTT | 9886 |
rs77803111 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905164 | TAAAAAAAAAAAAAA[A/T]TTCAGGCTGGGCATG | 9886 |
rs77832607 | snp | A/C | 0.0452528 | 0.143452 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002227 | TTAATATTAGAAACC[A/C]GCACATTTATACGTT | 9886 |
rs77877163 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880327 | TACAAGGTGCTTATG[C/G]CTTATGCACTCTGGC | 9886 |
rs77971786 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999993 | AAACTCATTGTTTAA[C/T]TGACAGGAAACATGC | 9886 |
rs77972797 | snp | A/C/G | 0.0471551 | 0.14613 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978985 | CTGCCAAATCTCCCC[A/C/G]TATGTATCATGTGTC | 9886 |
rs78067041 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978888 | TTCCTCTACTCACTT[C/T]CTTTTATAGAGGCCA | 9886 |
rs78159256 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903781 | ATGACAGTGTCCCAT[A/C/T]GTTAGTTTCAGGGTT | 9886 |
rs78162059 | snp | A/T | 0.0452528 | 0.143452 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002805 | CCTAGTTGCCTTTTA[A/T]TGAATTCTTTCCTTT | 9886 |
rs78163559 | snp | A/G | 0.149665 | 0.228982 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896096 | GAAGGCACAAGACCT[A/G]CAGCTAAGAATATCT | 9886 |
rs78179487 | snp | G/T | 0.0973687 | 0.197999 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936800 | AGCTCTAAAAGCAAT[G/T]AATTCCTTGGTAAAA | 9886 |
rs78188719 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914539 | GGGAGAATGTTTAGA[C/G]TTAGTAAAAATGGAG | 9886 |
rs78205528 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927199 | ATGAAAGCTATAAGA[C/T]ATTAAGGACACAAAA | 9886 |
rs78205583 | snp | C/G/T | 0.02016 | 0.0983543 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881419 | CTAAGTGCTCTAAGA[C/G/T]GTTAGTAATTGTTAA | 9886 |
rs78214740 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951403 | TATCCTTCTCTCTGC[A/C]CACAATTTCAGAGTA | 9886 |
rs78239826 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965988 | GGAATCTTACAGACA[A/T]TAAATATATAATTTT | 9886 |
rs78249234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901191 | ATGTGATTTCTGTGT[C/T]TGCAATTCAGAACTT | 9886 |
rs78256533 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884060 | AAGAGGCCATCAGGA[C/T]AACTCTAATATTTTT | 9886 |
rs78273609 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920621 | GTAGGTTCTGATTTG[C/T]TTTTTTTTTTTTTTT | 9886 |
rs78401589 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949022 | ACAGCACAGGTCTAA[C/T]AGGCTGTTGGGCTCC | 9886 |
rs78489194 | snp | G/T | 0.030278 | 0.119257 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906618 | CCAACCGTGAAATGA[G/T]CCTATTTTGCAGGCT | 9886 |
rs78522623 | snp | G/T | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876359 | TAAACTAAGTGTTCA[G/T]AGAAGTCTAGAGTTC | 9886 |
rs78547823 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979064 | TGGCTTCCTTGTCAT[C/T]AGTAGGTAGGTATTT | 9886 |
rs78590627 | snp | A/T | 0.0869089 | 0.189476 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910328 | TTTTTTCTCCTTTTT[A/T]AAAAAATAAACGTTA | 9886 |
rs78593665 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954715 | AAGGAAATGTGACAA[A/T]ATTATTTTTGAAATT | 9886 |
rs78609195 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908798 | GGGTCTGTGTCAGGA[C/T]GCCTGGAGGCTGTGA | 9886 |
rs78620841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920558 | CAGGAGTTTGGATCT[C/T]ATTCTAAATGCAGTG | 9886 |
rs78626044 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940669 | AATTTAGCGGTTCTG[A/G]ATGACTACATAATCT | 9886 |
rs78655696 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896979 | AAACAAAAAAAAGCA[A/T]TTTTTTTCAGTTATC | 9886 |
rs78670918 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930987 | ATCTCTGTCATGTAA[C/T]AGGAAGCAATATTGA | 9886 |
rs78676343 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949561 | TTGGTGTAGGAATCA[A/G]CTAAAAAGTGATGTC | 9886 |
rs78732863 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928387 | TTCCCATGTTTACTG[C/T]AGCACTACTTACAAT | 9886 |
rs78852472 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922221 | AAAAGGGAGGCACAC[A/G]TACCCATTACATATG | 9886 |
rs78872599 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932286 | TGGTTCAGGCAAACA[G/T]AGAATTCTGTAAATG | 9886 |
rs78965457 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887299 | TAAAATGAATGAACT[A/G]AGTCTTTAGGAACCA | 9886 |
rs78988480 | snp | A/C | 0.0944967 | 0.195752 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916836 | GCAGATTATCCTGGA[A/C]TATCTATGTGGGTGC | 9886 |
rs78995781 | snp | C/T | 0.141596 | 0.225274 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002938 | TTCTTCTTCTTATTA[C/T]TATTATAATACTTTA | 9886 |
rs79010049 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992705 | CACAAATTTTGTAAA[G/T]TAGAATAGTATCAGT | 9886 |
rs79065851 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889722 | AGCTATTTAATCTTG[C/G]GTAAGTTACTTAACC | 9886 |
rs79078979 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896318 | TTGAAGAGTCAGTTT[A/G]AAAATAATTGGGAGT | 9886 |
rs79109262 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902038 | CTCATTTGGCACTCC[A/G]CTTTCCAAGGACAAT | 9886 |
rs79191323 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986833 | CCTTAAATACAAAAC[A/C]AATAACTCCCAATTA | 9886 |
rs79238095 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932941 | CTTCTGAAGCAGCAG[C/T]GTGACCACCTGCTGT | 9886 |
rs79277349 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942872 | GTATTTTTTTTTTTT[C/T]CTGTTTAGAGTATGT | 9886 |
rs79288593 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876544 | TGACAGTTTCAAAAA[C/T]AAATAAAAATGTATC | 9886 |
rs79293407 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947687 | TGCTGAATTAAATTT[G/T]TATTGCATGGATGTA | 9886 |
rs79333948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939539 | TCTCCTACCCTTGTC[A/T]ACACACACTTTTTGG | 9886 |
rs79344944 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965019 | CCTTTGGGAGAGAAT[C/T]TCACAACTTTAGGGT | 9886 |
rs79366628 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891969 | TTATAAAGGGCATCC[A/G]CCTTTGCTCGGTTCT | 9886 |
rs79497531 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928330 | GGTATATATCCAAAA[-/C]AAAAAAAAAAAGAAA | 9886 |
rs79524467 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898261 | GAGTGTCTGACCTTC[C/T]TTGGGGCTTCAAGCT | 9886 |
rs79570598 | snp | C/T | 4.94279e-05 | 0.00497107 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888912 | GGCAGCTTCATTTGT[C/T]CCCATGGAAGGACAC | 9886 |
rs79571401 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906519 | GGGAAGATATGGGCT[C/T]TGGAGTCAGACAGAT | 9886 |
rs79574119 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948086 | TTGAATATATTTTCA[C/T]TGGCTTTTTTTGCCA | 9886 |
rs79704122 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919336 | TATTATTGACAGGAA[A/C]AAAGGAAAATGTTAA | 9886 |
rs79756968 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916723 | CCCTGAATACGTCCA[A/C]GGAATCCGCGGAACT | 9886 |
rs79805068 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928285 | AAACTAAAAATCAAA[C/G]TATCTTATGAGCCAG | 9886 |
rs79857508 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942873 | TATTTTTTTTTTTTT[C/T]TGTTTAGAGTATGTT | 9886 |
rs79920397 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884936 | TGTCCTTTTTTTTTT[A/G]GAGACAGGTTCTCAC | 9886 |
rs80020247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881525 | GCCTCTCGTGATAGC[A/G]CAAGAGCCTGGGGCA | 9886 |
rs80029192 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950149 | TTTTTATGGTCATCT[C/G]TCTGACTTTGTTTAG | 9886 |
rs80032508 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907168 | AGTCCATTAAACCTC[C/T]TTTTCTTTATAAATT | 9886 |
rs80033385 | snp | A/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966509 | ACCCTATCTCTAATT[A/T]AAAAAAAAAAAAGTT | 9886 |
rs80060452 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906401 | GTGAGTGCTGGTCTT[C/T]AGGGTCTACACAGTA | 9886 |
rs80097554 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925015 | GGCTTGAGCCATCCT[C/G]TTGGTGATAAGTGAA | 9886 |
rs80098258 | snp | A/C | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887088 | TTTAAAAAAAAAAAA[A/C]CAGAATCCAATTGAG | 9886 |
rs80149331 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872605 | CTAAACAACCGTGGC[A/C]TCTGGAAGGCACCAG | 9886 |
rs80165793 | snp | A/T | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912671 | ATCTTCCTGAGACCA[A/T]CCAAGAAGGTTTAAA | 9886 |
rs80248114 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880547 | GAAAACGACAATTAT[C/G]ATTCCATAAATAAGT | 9886 |
rs80327316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937835 | CTAATATGTTAAAAG[A/G]CTTTCTTTCGAGATA | 9886 |
rs111316408 | snp | A/G | 0.000181601 | 0.00952719 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911537 | GTAGTCCATGTCAGC[A/G]TCCATTTATGAAACT | 9886 |
rs111375715 | snp | G/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982466 | TCACATTACTCCAGG[G/T]TTTCTCAACCTTGAT | 9886 |
rs111403545 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880128 | GATTTGGCTGTCTGA[A/G]TTGGGGGGGTGGTCC | 9886 |
rs111403654 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875542 | GTCCTCTAGACTTTA[C/G]ACACGTTCCTGTTTG | 9886 |
rs111462268 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905816 | CTAACTCAAAATGCT[A/G]TATCTAGACACACTC | 9886 |
rs111541505 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980371 | AAGGTTATGAATATA[C/T]GATAAAAAAATGATT | 9886 |
rs111581902 | snp | G/T | 0.0225045 | 0.103662 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944755 | AGCTGCTGACTAAGG[G/T]CTGCATTAGCCCAGC | 9886 |
rs111609986 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906419 | GGTCTACACAGTACT[A/G]TGTAAGATTCAGAAT | 9886 |
rs111611242 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897412 | GTCTTCTTAGTTTGA[C/T]TTTCCTTTTCTAGTA | 9886 |
rs111637879 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918783 | TGGAGTTTCACTCTT[A/G]TTGCCAGGCTGGAGT | 9886 |
rs111654051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913008 | TAATGGCTATGGTAA[A/G]GAAACTGTTCAGAGT | 9886 |
rs111662428 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928831 | TGAGGTTATGGAAAC[C/T]CCAATGTAGTAGTCT | 9886 |
rs111662510 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956243 | AAACATAGAAAAGAT[A/C]CAGTAAAAATATAGC | 9886 |
rs111670359 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895894 | TAGGAATCAATGGAC[A/G]CAGTGACAGAGCTAT | 9886 |
rs111741816 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920512 | GAAAGGTAGGTGGGG[A/T]TAGATCATACTCAGC | 9886 |
rs111749907 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003368 | TATTGTGAATAGTGC[C/T]GCAATAAACATACAT | 9886 |
rs111759951 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881207 | ACCATGATTGTGAGG[C/T]CTCCCAAGCCATGTG | 9886 |
rs111762212 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875798 | GAGCTTGAGTCCAAG[A/G]CTTCCAAGCTGAATT | 9886 |
rs111785773 | snp | A/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919772 | ATGATTCTCACCAGG[A/G]CTCTCTGACAGTGGA | 9886 |
rs111899600 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988089 | GGCGCCCACCACCAC[A/G]CCCGGCTAATTTTTT | 9886 |
rs111941264 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966949 | CACTGGGGATACAAG[A/T]GTAAGCACGACAAAG | 9886 |
rs111967885 | in-del | -/TAT | 0.116488 | 0.211364 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924242 | AATGATACGAATGAC[-/TAT]AAATTTCACCAAGAC | 9886 |
rs112018350 | snp | A/C | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974617 | GTTTAGAGGAAGTAA[A/C]CAATATGATCAGTGT | 9886 |
rs112056365 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955552 | TCCCAAACCACAGAG[A/G]GTTGCTAGCTATCAT | 9886 |
rs112102366 | snp | A/C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990506 | AGCAATTTCTCTTTA[A/C/T]TTTAATTCAAAAATA | 9886 |
rs112102727 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947131 | GGAAAAGAGAGAAAA[G/T]GAATCATATCAAATA | 9886 |
rs112210848 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904946 | TTTTCCAAGACCTCT[A/T]GGTACCATATATTTA | 9886 |
rs112216453 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986974 | TGATTGCCGGTGGCT[C/G]CAGGCCAGTTGCTGC | 9886 |
rs112239033 | snp | A/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925516 | ACCTTATAATATATC[A/G]TAAAGAACTAGAAAA | 9886 |
rs112239111 | in-del | -/T | 0.461037 | 0.134028 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920956 | TTTGTTTTTTTTTTG[-/T]TTTTTTTTTTTTATG | 9886 |
rs112259086 | snp | A/C | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950391 | TTAAAAATAAATTAC[A/C]TTTATGTGTCACAGC | 9886 |
rs112266728 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898962 | CAAAAACCGCAATTA[C/T]GTTTGCACCAACCTA | 9886 |
rs112274177 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951397 | CAATAATATCCTTCT[A/C]TCTGCACACAATTTC | 9886 |
rs112298642 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874598 | CAGGGGAGGCACTAC[G/T]GGGCTTCATGGAATT | 9886 |
rs112308913 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955339 | AACCACCACACCCAG[A/C]CAGCAAGGGGAACCT | 9886 |
rs112333155 | in-del | -/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891713 | CAAAAAGTTCAACAT[-/T]AAAAAAACATAAAAA | 9886 |
rs112348134 | snp | A/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963493 | AGAATAAAATATTTA[A/G]ACAGCAACATTACAA | 9886 |
rs112408435 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974706 | GCAGTTGATTCTAGA[C/T]AGAGACACAAGTTTA | 9886 |
rs112411239 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961861 | TCACCCAGGCTGGAG[G/T]GTAATGGGATGATCT | 9886 |
rs112468563 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002577 | GGCTAGAGATAGCTA[C/T]TATTTTTAGCAGAAA | 9886 |
rs112501745 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886596 | GGCATGTTTGTTTTA[C/T]GTATATTTTTAATTT | 9886 |
rs112509297 | snp | C/T | 0.0383715 | 0.133092 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871282 | AGTGAGAGTCAGCTT[C/T]CCTTTTTGTCCAGGC | 9886 |
rs112516474 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965733 | TCTCATGGTCTATCC[A/G]TAGTTGGGGAATAAA | 9886 |
rs112531042 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955284 | CTGATCTCGTGATCC[A/G]CCTGCTTCGGCCTCC | 9886 |
rs112550453 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893897 | AAACCATCATTCTAG[A/G]TTAAAATGTGCTGAA | 9886 |
rs112637448 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879182 | TAAACCCAGGGAGTA[C/T]GATGCGAAAGTGTAT | 9886 |
rs112661265 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894600 | TTTTTATGGGCTGAG[C/T]TTTCTATTATTCATA | 9886 |
rs112670462 | snp | A/G | 0.0944967 | 0.195752 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944963 | ACTGTGGCCTCCATG[A/G]GCTGTCTTGGTCTTC | 9886 |
rs112727132 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962546 | CTTTTTAGGGAAATT[C/T]CCATACTTCAGGAAG | 9886 |
rs112737716 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937718 | CCCAGAGAGACCACT[C/T]GGCCTGTTGTGTTCA | 9886 |
rs112796685 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890363 | TACATAACACAACTA[C/T]GACCTGGCGGCAGTT | 9886 |
rs112819081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910473 | CAAAGCAAATAACAT[C/T]AGACTCTGCCAATAT | 9886 |
rs112824276 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902502 | AAACAACCTATAATT[A/G]GAAAAGCGTTATTAT | 9886 |
rs112843642 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961964 | AGGCATGCACTACCA[C/T]GCCTGGATAATTTTT | 9886 |
rs112848712 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932209 | GGCAGACGTCTACAC[A/G]TTTTCAGTGACAAGG | 9886 |
rs112867303 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915159 | TTTGTTACACATAAA[A/G]AAACATTAAATTATG | 9886 |
rs112872385 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907125 | TTCTGCCATGATTGT[C/G]AGGCCTCCCCAGCCA | 9886 |
rs112879113 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994088 | TTAGAAATTATTGCT[A/T]TGTGTTAGGATAACA | 9886 |
rs112883588 | snp | G/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877764 | CTGTCTGATGCAATT[G/T]GATTAATTCATATCA | 9886 |
rs112906192 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949799 | AGAAGCATTAGATAC[C/T]GTGTACTTTTCATTG | 9886 |
rs112931897 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954051 | AACCACTACCTTTTT[A/T]AAAAGTGTATGTGTG | 9886 |
rs112933076 | snp | A/G | 0.0966517 | 0.197444 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943790 | GGTCCCCGGCCTCTC[A/G]GAGAGGCGAGGGAGG | 9886 |
rs113032812 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907361 | AACTCTTGAGTTGAG[C/T]GACATCCCTTTAAGA | 9886 |
rs113076413 | snp | A/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877795 | TTCTACACAAGACAG[A/T]CCTATTTTGGGTGAT | 9886 |
rs113086561 | snp | C/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918411 | TCCCAGGAAGTTCTG[C/T]GCATGCCCACTCCCT | 9886 |
rs113103661 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911157 | TTCCTGGAATCATCT[A/G]TCTCAACCCTCATTC | 9886 |
rs113104593 | in-del | -/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001822 | GCCATTCTCCGCTCA[-/G]GGGCCCGAGGGGCCG | 9886 |
rs113141507 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929758 | ATAAGGAGAAATTCA[C/T]AACAATAACAAATAT | 9886 |
rs113148165 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920954 | GATTTGTTTTTTTTT[C/T]GTTTTTTTTTTTTTA | 9886 |
rs113200174 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905381 | CTTGAACCTGGGAGA[C/T]GTAGGTTGCAGCAAG | 9886 |
rs113203307 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901663 | TCAGAAAGTTCCAGT[A/G]TAAACACATCACAAA | 9886 |
rs113227903 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897971 | GGCTTTGCAAAGAGC[C/T]GGGATTACAGGCATG | 9886 |
rs113244256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940493 | TCCAAATCCATCTAC[A/G]TGGTGCCTTTCAGAC | 9886 |
rs113254310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925996 | AGCACTTTGTGGGGC[C/T]GAGGCGGGCAGATCA | 9886 |
rs113280455 | snp | A/G/T | 0.0387552 | 0.1337 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884813 | AGAGAGTAGAAGAGT[A/G/T]ATTACCAGAGGCTGG | 9886 |
rs113318033 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945239 | TGTAAAGAGATCACT[A/G]GGGAATAAAGACACA | 9886 |
rs113325177 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889762 | ATTAGTTTTTCCATC[A/T]GTAAGACAGGAATAA | 9886 |
rs113334669 | in-del | -/A | 0.132066 | 0.220435 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905573 | GTCTGAGGCAGAAGG[-/A]GAAAAAAAAACCAAA | 9886 |
rs113353918 | snp | A/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990399 | AAGAATCTTTTTGAG[A/G]CAGATGCAAGACATG | 9886 |
rs113363552 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873715 | CCAAGTGTGAACAAC[A/C]AGTTTTGATGGGGGC | 9886 |
rs113368160 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993022 | AGTCAATGTCTTAGG[C/T]GCATGCCTCTTTAAG | 9886 |
rs113377782 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955075 | TTTAAGATGTAGTCT[C/T]GTTCTGTTGCCCAGG | 9886 |
rs113419433 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869832 | CTACTGCCTTCTCTT[C/T]TGTCATGACAAGGTG | 9886 |
rs113460697 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931169 | ACGTCTTATTTTTTT[A/T]AAAAAATGTGAGATA | 9886 |
rs113474896 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996637 | TTTTCTCAGGAGGAC[C/G]TCCAGAGCTTTTATC | 9886 |
rs113484424 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872043 | CTTATGTCATCTCAC[A/G]TTAATATGTGACCAC | 9886 |
rs113489177 | snp | A/T | 0.0908922 | 0.192833 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885756 | TCCTCTTGTACTTGG[A/T]TTTGATAGTACCATG | 9886 |
rs113490752 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871021 | TTACGTAATAATGCT[A/C/T]GGTGGTCATGTGGGC | 9886 |
rs113516048 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924645 | ACTATAGACCAAATG[A/G]ACCTAACAGACATTT | 9886 |
rs113526928 | snp | C/T | 0.00358391 | 0.0421795 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893028 | AAGAAGCTTGTATTG[C/T]CTTTTAACAGGTTTT | 9886 |
rs113549090 | snp | A/C | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941698 | AAAGTCAAAGACAAA[A/C]TTTTTAAAAGACAAA | 9886 |
rs113566095 | snp | A/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933518 | CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9886 |
rs113572273 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988705 | TTATTCAATCCACCA[C/T]TGATGGGCACCTAGG | 9886 |
rs113626426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907230 | GTAAGAACAGACTAA[C/T]ACAGGGACTGAAGGG | 9886 |
rs113653742 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919015 | CCTCCCAAAGTGCTG[C/T]GATTACAGGCATGAG | 9886 |
rs113703862 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946009 | ATGGTAAAACCCCGT[A/C]TCTATTAAAAATACA | 9886 |
rs113720399 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908532 | AGCTATAATTATGAT[A/T]CCTCTCCTTCACAAA | 9886 |
rs113759756 | snp | A/G | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922072 | CTAGTTTCTAGAGCC[A/G]ATTTATAAATGTTAA | 9886 |
rs113783815 | snp | C/T | 0.0174175 | 0.0916809 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869406 | ATCACACACACAATA[C/T]GATGTCTGTCCTTAA | 9886 |
rs113821031 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875582 | CCACTCACATCACTG[C/T]AATCCTTAATATCCC | 9886 |
rs113845217 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906926 | TGATTCTCACATGTC[A/G]TGATGTCGTGGGAGG | 9886 |
rs113890954 | in-del | -/TT | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918752 | TTTCTTTTCTTTTTC[-/TT]TTTTTTTTTTTTGAG | 9886 |
rs113943885 | in-del | -/GA | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893118 | ATTAAAAAAAAAAAA[-/GA]CCAGATATTAAAAAA | 9886 |
rs113953181 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987347 | ATATCTTTTTGGATG[C/T]TTCATCCCCATCCTC | 9886 |
rs114029871 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906109 | TCTAAGAATAAACTA[G/T]ATAATAAATGGGTTC | 9886 |
rs114078267 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990463 | CAGACAGAACCAGTT[A/G]CAACTGTATTTCCTG | 9886 |
rs114096413 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870192 | GAAGCAATGACTGAC[C/T]GCCTCACGAAAGCTC | 9886 |
rs114113303 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928823 | TAAATGCTTGAGGTT[A/G]TGGAAACCCCAATGT | 9886 |
rs114157433 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954417 | AAACATATTCAATGA[C/G]CACTGAATGAATTCT | 9886 |
rs114167858 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911109 | AAGTTTCCTTATTCT[A/G]TCTGACGGGATTTAA | 9886 |
rs114174483 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932513 | AATACTTTCTTAAAG[A/T]AAAAAAAAAAAAAAA | 9886 |
rs114240794 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939797 | TTCAAATGTTTCCAG[A/C]CATTTTTAAAGAGGT | 9886 |
rs114246287 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876340 | AATAATAGCATTTAA[C/T]AACTAAACTAAGTGT | 9886 |
rs114249746 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957939 | AGTCTAAATGAAACT[A/C]AAATTCACAACCATA | 9886 |
rs114277024 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905156 | ATAATACTTAAAAAA[A/C]AAAAAAAATTCAGGC | 9886 |
rs114327491 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923336 | GTAAAAGAAGATAAT[A/G]TACATTTATAAACTA | 9886 |
rs114351929 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977963 | CACAGGAAAGAAATA[A/G]ATCACTTATTAAAGG | 9886 |
rs114352947 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930633 | GAAAGCTGTGAACCA[G/T]GTAGCTGCTTATGAA | 9886 |
rs114354740 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950944 | ATGTTTTGCTCTGCC[A/G]TTGACTTGCAACTGC | 9886 |
rs114365431 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891897 | ACTGAATCGTGGGGG[C/T]GGTTCCCCCATGCTA | 9886 |
rs114386730 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918329 | CCTTTGGTGGTACCC[C/T]AACCCAACCTTCAGT | 9886 |
rs114443875 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913406 | ACATCCTGGGTGGGG[A/G]AAAAGAGTCTTTAAA | 9886 |
rs114456020 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956142 | TATGGTATAGCCCGT[A/T]GTTTCTAGGCTGCAA | 9886 |
rs114466385 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952780 | TAGTATTTTATATAT[C/T]CAAAGTTTCATGTAG | 9886 |
rs114502870 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902039 | TCATTTGGCACTCCG[A/C]TTTCCAAGGACAATT | 9886 |
rs114529219 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981748 | GCAAAAGTTAAAAAA[C/T]TAACAGTCACTTGGT | 9886 |
rs114533728 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953193 | AAGGTTAGCCTCCTC[A/G]TGAGTGTATCGTTTG | 9886 |
rs114547551 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904094 | CAACCTCCCGAGTAG[C/G]CACAACACCTGGCTA | 9886 |
rs114594329 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906408 | CTGGTCTTCAGGGTC[C/T]ACACAGTACTGTGTA | 9886 |
rs114598647 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949764 | TTCTTGGCATTTCCT[A/G]TGATTACCCATTTAA | 9886 |
rs114603849 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969928 | ACCTGAGAGAAGACT[A/G]TAGGACTTCAAACAT | 9886 |
rs114604709 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921961 | TCACCAAATGGGAAG[C/G]TGGTGGTGGGGAGGA | 9886 |
rs114652746 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928949 | AAGCATGGCTTGGGA[A/G]GCCTCAGGAATCTTA | 9886 |
rs114733060 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923437 | CAAATTGAAAGCCGT[A/G]CTGGCAACAGTACAT | 9886 |
rs114789509 | snp | A/C/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873039 | GTGGATCCCTAGAAC[A/C/T]TACAGCATGCTTCCT | 9886 |
rs114886957 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910036 | GCTTGGAGTACCTAA[C/G]TAATAAAATCCTGTA | 9886 |
rs115012285 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909971 | ACTGGCTTGTAGAAA[C/T]AGAAGAATCTTCAGA | 9886 |
rs115019961 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901102 | GACCATCTTGCTTTT[A/G]AAAAACACACAAAAC | 9886 |
rs115029484 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990634 | CTTGCTCCTCTGCCC[C/T]CCATGACCCAGGAAT | 9886 |
rs115029668 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952906 | CAGGTGTCGATGAGC[A/G]ATATGCCCTCACAAC | 9886 |
rs115076482 | snp | C/T | 0.00560247 | 0.0526294 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889098 | ACCAAACTGGTCAAA[C/T]ACGCTTGTTTCATAG | 9886 |
rs115108582 | snp | C/T | 0.030278 | 0.119257 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883745 | GGCAGCTACTATTTA[C/T]TGAATGCTTCTGAAC | 9886 |
rs115126586 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959583 | ATGAAACAAACAAAC[A/G]AACAAATAGCTGAAC | 9886 |
rs115150271 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906433 | TGTGTAAGATTCAGA[A/C]TGTACCAGGAGGAAA | 9886 |
rs115152911 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928555 | GTTCTCACTCATATA[C/G]AGGAGCTCCAAAAAA | 9886 |
rs115220234 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996434 | CCTAGTTCAACTATA[C/T]TTTTCACAGTCACCT | 9886 |
rs115234868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977379 | ACTTATGTATGGCTG[C/T]TTATGCTCCTCCATA | 9886 |
rs115306914 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968630 | CTGATTTTCAAAATG[A/G]GGAGGGAGATAGTTT | 9886 |
rs115330641 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993145 | GTAAAAAGAGGAGCT[C/G]TAAGAAAATGGAGAA | 9886 |
rs115370809 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998094 | GCCGTAAAATATGGG[C/G]TTGTACTAGGTGCAG | 9886 |
rs115422528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | RHOBTB1 | GRCh38.p7 | 10:60885822 | GTCTTCATGGATGAG[A/G]ACGGCTCTGAGGATG | 9886 |
rs115424389 | snp | C/G/T | 0.0182182 | 0.0938163 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970538 | AAGTTCAATGCTTCA[C/G/T]ATTTACCTGAGGAAC | 9886 |
rs115493921 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984040 | TATACCACTTAAAAT[A/C]TCTCTAACTTTCTGA | 9886 |
rs115508078 | snp | A/T | 0.0391387 | 0.134304 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912533 | CCACCATGCCTAGCC[A/T]TAAAAAAGATATTCT | 9886 |
rs115546758 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998499 | ACTTCGGTTTGTAAT[C/T]GGCTCCGTGAGGGAT | 9886 |
rs115569032 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937531 | CCATGTAGAAAACAC[A/G]TTAGCTACTTAGGAA | 9886 |
rs115602593 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899468 | TCAGCTACCGCGCTA[C/T]ATGGGAGGTCTCTGG | 9886 |
rs115688307 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928100 | CGTCATCAGAGAAAT[A/G]CAAGTGAAAACTACA | 9886 |
rs115730426 | snp | C/G/T | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965148 | ACATATACAAAGAAA[C/G/T]TTACCATTCAGTAGA | 9886 |
rs115741337 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914990 | CAGATGTGGAATTTC[A/C]AGGAAGCATTCACTG | 9886 |
rs115797665 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934686 | CCTTAATGATCAGCT[C/G]CCAAATTTAGCCTTT | 9886 |
rs115855560 | snp | C/G/T | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958100 | TGAAAAGACTCAGTA[C/G/T]ACAAAACAGCCAACG | 9886 |
rs115857245 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897554 | TCAGGTAAATTTTAC[A/G]GGCAATGAGAAGGAC | 9886 |
rs115908905 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896509 | GAGTACAGGGTACAT[C/G]AGATTGTAAACTCCA | 9886 |
rs115910550 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877450 | AGGTTACAGGACAAA[A/G]TCACCTGGTCAGTAA | 9886 |
rs115911750 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951011 | CATGCAGAAACTAGG[A/G]AAATAAGTGGACTAC | 9886 |
rs115924718 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951748 | GCAGGAAAGTGCCCA[A/G]TGGTTGTTAATAATG | 9886 |
rs115973977 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874753 | ATGGGGGTGGGGACC[A/G]TTTTGTTTATTCAAA | 9886 |
rs115993486 | snp | A/C | 0.040671 | 0.13668 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914025 | CAAAATTGAGTCAGG[A/C]GGAAGGCCAGAATTA | 9886 |
rs115995419 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952245 | GTGATCACTGTCAAC[A/T]CTGATCACCCATGAA | 9886 |
rs116041719 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925675 | AAATCTTTAGCCAGA[C/T]TAAGAAAAAAAAGAA | 9886 |
rs116042828 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948561 | ATGCTGTCCATCTCT[C/T]TGCTCTGGATGCAGC | 9886 |
rs116045534 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901837 | TGCATATATTCCTTA[A/T]TCTCTTTGCCCATTG | 9886 |
rs116099863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930820 | TCTTCTTCATCCCTT[C/T]TTACAGGGCTAGCCA | 9886 |
rs116103464 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973633 | AGAAGGCCCATGAAG[C/T]AATACTAGACTAGGA | 9886 |
rs116109654 | snp | C/T | 0.030278 | 0.119257 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907226 | CAGTGTAAGAACAGA[C/T]TAATACAGGGACTGA | 9886 |
rs116270049 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924564 | AGGGACTTCAGTATC[C/T]CACCTTCAGCATTGG | 9886 |
rs116297970 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912260 | GTATATGGAATCTCA[C/T]GCTGTCACCCAGGCT | 9886 |
rs116301884 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948191 | CTGTTGAGTTTTTAA[C/G]AGTTTAAAAAAATAC | 9886 |
rs116366278 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962174 | TAAGTGGAAATTTTC[A/C/G]TAATGAGCCACAAAT | 9886 |
rs116370597 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973930 | CTAATGTTTGAAGTA[A/G]TTTAGGCCAAATAGT | 9886 |
rs116391455 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881623 | GTCTCTTCATCCGTT[A/T]CATGGGAGGAATTTG | 9886 |
rs116521110 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998171 | TTATGGTACTCAGAT[C/T]TCCATTCATAATTCA | 9886 |
rs116522806 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907913 | AAAAGAACTCAACCT[C/T]TTACTCAATGGTAGC | 9886 |
rs116583839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888108 | GGAAAAAATAAGTAC[A/G]TATAAATGTTAGCTA | 9886 |
rs116585978 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957838 | ACCATTCCCACTGTA[C/G]GGACAGGAAAGCTGA | 9886 |
rs116612905 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993893 | AATTTTTTGGTGACA[G/T]TTAGCTCAATAGTGC | 9886 |
rs116613238 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953833 | ACACAAAGACACATG[A/C]AAAACCCTTTGAAAT | 9886 |
rs116769344 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970550 | TCACATTTACCTGAG[G/T]AACTAATAAATTTTT | 9886 |
rs116773384 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980726 | AACATTGATGAAAGG[C/T]GAATTTAGAATTTAG | 9886 |
rs116833955 | snp | A/G | 0.0201759 | 0.0983916 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948952 | AGTGGTTTAGTGGCA[A/G]CTTCCTTGAACAAAT | 9886 |
rs116960034 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991189 | CCCATATTCCACACG[A/G]TAGCCAGAAATATAT | 9886 |
rs117000196 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906910 | CGAATCGTAGCTCCC[A/G]TGATTCTCACATGTC | 9886 |
rs117067067 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964367 | GGGGACACATGGAAA[A/T]TAAGCAAAGTCTCTC | 9886 |
rs117076930 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928508 | ATTATGTTAAATAAA[A/G]TAAACCAGGCACTAA | 9886 |
rs117078537 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992622 | ATCTCAATAAATAGG[C/T]GAAACTCAAATGTTG | 9886 |
rs117131440 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886977 | ATAACCATACTATGA[C/T]TACACCTAAGAAAAT | 9886 |
rs117136329 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002635 | TAAAAGTATGATATA[A/G]CTGGGATGTCAGATC | 9886 |
rs117204846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980065 | CAATGGAGGTTCTGA[A/G]TCAAGGAGCAAAATT | 9886 |
rs117269652 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973194 | GAGAAAACAAGCAGC[A/G]TCTTTCCTCTATCAA | 9886 |
rs117313674 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890340 | CTCACTGCTGCAAGA[A/G]AAGTCTTTACATAAC | 9886 |
rs117349240 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903869 | TTTCAACGAGACTAA[C/T]TTAAAGTTCCATAAA | 9886 |
rs117351833 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944992 | TCCAAGACAGCCCAT[G/T]CCTCCTCACAGAAAC | 9886 |
rs117371509 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962330 | GATACTTACCTACAA[C/T]AGATAATATATCAAA | 9886 |
rs117373805 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976183 | TGCAACGGTGGCACA[C/T]AAGGAAAGCAGTAAC | 9886 |
rs117459939 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950247 | GTATAATGTGTATCT[C/T]TGACATTTTAAAAAG | 9886 |
rs117467631 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964817 | TAATTTCAAGTGGAG[A/G]GCAAAGATCAACTTG | 9886 |
rs117507594 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914816 | AAGAATTTCTGTGTC[A/G]AAGGTGAGAATAACA | 9886 |
rs117521786 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925023 | CCATCCTCTTGGTGA[C/T]AAGTGAACTCTTGCT | 9886 |
rs117544792 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970791 | ACAGTGCAAGATTAA[C/T]GCTATGGTTTTCTAT | 9886 |
rs117578432 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960328 | CCCCTATTGATTATG[A/C]TGGCGAATTTAATCA | 9886 |
rs117580332 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959866 | AAGAAACCTCAAAGT[A/G]TTTCTTTGAAGATTA | 9886 |
rs117616792 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980480 | ATTAAACAATTGTCT[A/C]TTATGACATTGAGAT | 9886 |
rs117665450 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899341 | TTCAACTCCGTCTGG[A/G]GTTCATATTCCTCTT | 9886 |
rs117680249 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919547 | CCTGAATCAAAACTT[C/T]ACAGAATTATATCTC | 9886 |
rs117691473 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949164 | TAAAATACCTTATTG[C/T]GTTCAGTCACTCAAG | 9886 |
rs117740160 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883445 | AGGAGATTAGCATTC[A/G]TGAGGTCAGCTCTGA | 9886 |
rs117868759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958911 | TGGCCCAGAGTAGGA[C/T]ATTTAAATAAAAAGA | 9886 |
rs117903959 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949914 | TAGACCAAAAGGTAT[A/C]CTTTTCTTATAGCAT | 9886 |
rs117909908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929533 | ACAAACAAACAAAAG[G/T]TACCCAGGCTTTAAA | 9886 |
rs117940118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952902 | GGATCAGGTGTCGAT[A/G]AGCGATATGCCCTCA | 9886 |
rs117989854 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892702 | AACCCATGGCTGATT[C/G]ATGGGATCCAGGAGT | 9886 |
rs118012519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958922 | AGGATATTTAAATAA[A/G]AAGACTTCATTTTTG | 9886 |
rs118035075 | snp | A/T | 0.0948562 | 0.196037 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886762 | AGGCTGGATTTAAAC[A/T]GCCGGGTTCCAGCAA | 9886 |
rs118035270 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947803 | GTAAACATTTGTGTA[C/T]AGGTTTTGTGTGAGC | 9886 |
rs118050390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999718 | GGATTAGACTGGAAA[G/T]CTATGAGGCTATTCC | 9886 |
rs118056323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974777 | TCTAATTACTTACTG[A/G]TTGCAGGAACCTGCA | 9886 |
rs118102092 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906956 | GGACCCAGTGGGAGG[C/T]AACTGAATCTTGAGA | 9886 |
rs118130243 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996375 | TTCAAAGCTTCAGAT[C/G]TCTTCCCACCCACAA | 9886 |
rs118182258 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980126 | ATAGGAGGCAAGGGT[A/G]GAAGCAAAGTGATCA | 9886 |
rs137913642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995370 | AGGAACCATCAGAGA[C/T]TGGAACCTAAGCAGT | 9886 |
rs137915565 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945707 | ATCCAATGTTTTTAC[A/G]AGGAAAGTTATCACC | 9886 |
rs137967449 | in-del | -/TATA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986412 | ATAAAAGATATATAT[-/TATA]ATATATATATATATA | 9886 |
rs137973477 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891945 | AAGTTCTCATGAGAT[A/C]TGGTGGTTTTATAAA | 9886 |
rs137982852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991892 | CACTTAGAAGAGTTT[C/T]GGTTCCATATTCATG | 9886 |
rs138003466 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955891 | TTTGTTACATTTATA[A/G]CAACTTTTAATTATT | 9886 |
rs138030166 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002640 | GTATGATATAGCTGG[G/T]ATGTCAGATCAGGGT | 9886 |
rs138038262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915387 | TAAATCCTGCTGATC[A/G]ATGTGGAGACCCTCT | 9886 |
rs138039971 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896248 | TCTGAAAGATAAAAA[C/G]AAACAGGCAAGTTCT | 9886 |
rs138092528 | in-del | -/GAAAA | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999254 | TTTAGTGAAGGAAAT[-/GAAAA]GAAAAGTCCACTAAA | 9886 |
rs138097417 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997303 | CTTCGGACCATTTGA[C/T]TGAGAAATCACCAAA | 9886 |
rs138109011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962053 | CCTGAATTGATCCGC[C/T]GGCCTCGGCCTCTTA | 9886 |
rs138154225 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975239 | AGAATCAGGGGAATT[C/T]GTCAGAATGTGTAAA | 9886 |
rs138192255 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884526 | TAAAAAGACAAAGAG[A/G]CTGTACTCCCATGTT | 9886 |
rs138240504 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923837 | TTTTTTCCTTGTCTG[C/T]CTCTCACCTTCCACC | 9886 |
rs138240569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887410 | GAAGTCAACATTTTA[C/T]GATGAAATTACACAC | 9886 |
rs138242545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883833 | TTTCCAGATCAGGAT[A/G]CTAGAGCCAAGAAAG | 9886 |
rs138276319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926464 | ATATCTAATACACAT[A/T]GATGCAAAATTCCTC | 9886 |
rs138281124 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873371 | AACAGATTGGGGTCC[C/T]ACTTGCCCTCAAGCT | 9886 |
rs138300581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937120 | GCTTTCTTCCGCGTA[A/T]GTGATGAATTGGATG | 9886 |
rs138306030 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921121 | GCCTGGCTAATTTTT[A/G]TATTTTTGTAGAGAT | 9886 |
rs138316357 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945049 | GTTCTGAGGACAGAA[A/C]CAGGGGTAGTTTTCA | 9886 |
rs138366944 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931597 | TTTTTAAAAAACTAA[G/T]GGGTATATTAAGTAT | 9886 |
rs138419014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983110 | TAACCAATTAGCATG[C/T]CATTATGGAGGAATA | 9886 |
rs138429711 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950895 | AGCTTCCACCAAATT[A/G]TATGAGGTAGAAAGT | 9886 |
rs138435074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897316 | CTTTGAAGACATGGT[C/T]GGAAAAGAATTGATA | 9886 |
rs138461650 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977692 | AAGGACCATTTCTCA[C/T]CCACATGAACCAAGG | 9886 |
rs138497554 | in-del | -/TT | 0.0170251 | 0.090679 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974911 | ATGGGGATGACTGTA[-/TT]TTTTATAAGCAAATG | 9886 |
rs138532356 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901441 | AGAGTGTATCTTGTA[C/T]GTTGACTTTAATAAG | 9886 |
rs138551351 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996750 | GGAATGCCAGATTTA[A/G]CAAATAAAAATATTA | 9886 |
rs138576487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915087 | TTTAAGAATGTGAAA[A/T]CACAGCCAAGGATGG | 9886 |
rs138580713 | snp | A/C/T | 0.000411803 | 0.0143437 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872266 | GGTGCAAACACCAGG[A/C/T]GGCCAACTGGTGGGC | 9886 |
rs138598770 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905647 | ATTTTATGCCCAAAG[C/T]GAGTGACTCCCTCAG | 9886 |
rs138634738 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891660 | GCCTAGAGGAGGGTA[A/T]TAATATCAAAATTTT | 9886 |
rs138665410 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988621 | TGCATTCACATTGTC[G/T]CAAGGGACATGATTT | 9886 |
rs138676308 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881302 | CAGCATGAAAATGGA[C/T]TAATACAATTAGTAT | 9886 |
rs138680245 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961299 | AGAGCTGGACACATC[A/T]GGATTAGAACCCTGG | 9886 |
rs138729318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930893 | CTCCGACAAATAAAC[A/G]AATCTTTCTTGGGAC | 9886 |
rs138743540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956523 | CTTAATTTTTAAAAA[C/T]CTTTTGGCTATTTTA | 9886 |
rs138903067 | in-del | -/ACAC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997065 | ACAGCATGGTTATGT[-/ACAC]ACACACACACACACA | 9886 |
rs138903492 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906364 | AAGAGGAACACTGGA[A/T]TATCAGAGCTCGTAA | 9886 |
rs138916135 | in-del | -/TTC | 0.0930568 | 0.194599 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002917 | CATTCTTCATTTCTT[-/TTC]TTCTTCTTCTTCTTA | 9886 |
rs138917834 | snp | A/C/G/T | 0.000216133 | 0.0103936 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888687 | TTCTTCCTCTGGGTC[A/C/G/T]ACACTCAATATCCGC | 9886 |
rs138930761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988340 | TTATATTCAAGGGAT[A/G]CATGTGCAGGTTTGT | 9886 |
rs138935169 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920955 | ATTTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTAT | 9886 |
rs138969758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938055 | AAAATGAAAAAGCAT[C/T]GAACAGATCACTTAA | 9886 |
rs138969844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880299 | TGTATGTATGTATAA[C/T]GGCCCCACATTCTAC | 9886 |
rs138974201 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970707 | CCGTGGTCAGAAAAG[A/T]GCTTACATAGCTTTT | 9886 |
rs139002419 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932845 | GGTGTTTAAAAACCC[A/G]TATTCATGAAGAAAA | 9886 |
rs139038569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978730 | TAGAACATAGTTCCT[C/T]TCTTCTTCTACTTCT | 9886 |
rs139041469 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967060 | AGGGTGGGGGTGAGG[G/T]AGCGATGCAGTATGG | 9886 |
rs139082859 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001080 | CGCGCGCGCGCACGC[-/GT]GTGTGTGTGTGTGTG | 9886 |
rs139094830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922464 | AAAAGTAACCACATA[C/T]CAGAAACTGGAAGGA | 9886 |
rs139120810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885723 | TCTTTTCCCTTTCTG[A/C]ACTACTGGGAGACAT | 9886 |
rs139162967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907586 | TTTCAAAGTGCAGAG[C/T]GTTACAACACTCATG | 9886 |
rs139183152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947229 | ATACTAAAATCATTG[C/T]TTGCTGATAGAATCA | 9886 |
rs139186815 | snp | A/G/T | 0.000595301 | 0.0172429 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888482 | TGACCACAGTCATGG[A/G/T]CCCCATCCGCTTTGA | 9886 |
rs139288389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953482 | AGTAGTACCTAAGCG[A/C]CTTTTGTCTTAACAG | 9886 |
rs139320380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998547 | GAGAAGAACAGAAAG[A/G]TGTTCAGAAGAAGAC | 9886 |
rs139397317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872789 | ATAAGAAGAGCAGGC[A/G]GTATGGGCAGGGTGG | 9886 |
rs139404457 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870659 | CCTAATACAGCAATC[C/T]GAACACCAGCGCACT | 9886 |
rs139464898 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934077 | ACATGTGTTCTTTGT[A/G]ACATAAAGAAATTTT | 9886 |
rs139497630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984831 | TTATTTTCAGTCTTA[C/T]GTACACATTTTAGAC | 9886 |
rs139529379 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940606 | CAGCTCACAATTTTG[G/T]GTTACCATGCTTGTG | 9886 |
rs139544052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903480 | TGCATGCTGCCAGAG[A/G]TTACCACCATGTTCA | 9886 |