| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs6697 | snp | C/T | 0.0733688 | 0.176922 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95793352 | CTATGGTATATTTTG[C/T]TCCCTTTTAAGACCA | 22836 |
| rs6815 | snp | C/T | 0.312104 | 0.242163 | utr-variant-3-prime, downstream-variant-500B | RHOBTB3 | GRCh38.p7 | 5:95795588 | AAACTACACACTCCA[C/T]ACCAACTGGGCACCA | 22836 |
| rs7622 | snp | A/G | 0.480461 | 0.0968913 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95795697 | AAGAGAAATCAAATT[A/G]GTGTTTAAACCCATT | 22836 |
| rs12089 | snp | A/T | 0 | 0 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95795637 | GGATGTTGGTGTCAC[A/T]CACACAGGTAGGTGG | 22836 |
| rs12351 | snp | G/T | 0.356597 | 0.226135 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95793547 | GATTAATTGCTCTAT[G/T]AAAATAAGGGGCATT | 22836 |
| rs14612 | snp | C/T | 0 | 0 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95793320 | AGTGGTAGTTTTTTT[C/T]CAAAGAGAACTAATA | 22836 |
| rs34893 | snp | C/G | 0.350114 | 0.229079 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95734359 | GTGTTGCATAACCCC[C/G]AGAGGAAACCCTGGA | 22836 |
| rs34894 | snp | A/G | 0.491629 | 0.0641526 | intron-variant, upstream-variant-2KB | RHOBTB3, SPATA9 | GRCh38.p7 | 5:95732879 | GAATGTTTTCCTTTA[A/G]TCTTATTTGAAAATC | 22836 |
| rs34896 | snp | A/G | 0.493718 | 0.0557446 | synonymous-codon, utr-variant-5-prime | RHOBTB3 | GRCh38.p7 | 5:95748427 | AAAAGAACTAGGAGC[A/G]ACCTATCTTGAACTC | 22836 |
| rs34897 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95750599 | atagtgctaggacta[C/T]gctcccaaatccagt | 22836 |
| rs34898 | snp | C/T | 0.493708 | 0.055737 | synonymous-codon, intron-variant | RHOBTB3 | GRCh38.p7 | 5:95755490 | GGACGTGGTATTTTA[C/T]AACCCCAATTTAAAG | 22836 |
| rs34899 | snp | A/G | 0.495329 | 0.0481013 | missense, intron-variant | RHOBTB3 | GRCh38.p7 | 5:95755497 | GTATTTTACAACCCC[A/G]ATTTAAAGAAAGTTG | 22836 |
| rs34900 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95757380 | TTCAAATCATGTAGC[A/G]ATAACCTGTTAGGCT | 22836 |
| rs40099 | snp | A/G | 0 | 0 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95756635 | caaactgtgcacaag[A/G]gttccaatttctcca | 22836 |
| rs42862 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95735171 | AGCTTTCCCATTTTT[C/T]TGCACTGTGTCCCAC | 22836 |
| rs45466 | snp | A/G | 0.495056 | 0.049474 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95752859 | caggtgtgagccacc[A/G]cgcccgggactctac | 22836 |
| rs185312 | snp | A/G | 0.496778 | 0.0400063 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95735111 | CAGTTGGAACTGAAT[A/G]AGCTGTGTGGTTTGG | 22836 |
| rs888807 | snp | C/G | 0.469049 | 0.120489 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95784495 | GTGATTGCTAATAAG[C/G]TGAGACATGAAAACA | 22836 |
| rs888808 | snp | A/G | 0.482384 | 0.0921818 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95783704 | AAAACAACAATTAAA[A/G]AAACATGCTGACCGT | 22836 |
| rs1060488 | snp | A/G | 0 | 0 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95794710 | GACTTTAGAATACAC[A/G]CAGTTTTTCCGACTT | 22836 |
| rs1129809 | snp | G/T | 0 | 0 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95791976 | gcccctattcaagat[G/T]cagttgctctagttc | 22836 |
| rs1801904 | snp | G/T | | | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95793270 | ACCGAAACCAATGTG[G/T]GTGTTAGAAAAATTA | 22836 |
| rs1862236 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95749036 | GCCGTGGCGCATATT[A/G]GGTTCTGCAGTCATT | 22836 |
| rs1984965 | snp | C/T | 0.147656 | 0.228091 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95752855 | TGTGAGCCACCGCGC[C/T]CGGGACTCTACGTTC | 22836 |
| rs1987521 | snp | C/T | | | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95765596 | AGCAAGTCAGGGCTT[C/T]CTATAAAATGAGGGG | 22836 |
| rs2042186 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95741150 | tggctaacacggtga[A/G]acccggtctctacta | 22836 |
| rs2059075 | snp | A/G | | | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95741546 | tttttttttttttta[A/G]aaacaggatcttgct | 22836 |
| rs2112401 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB3, SPATA9 | GRCh38.p7 | 5:95733263 | TGATGCTGTTCATAA[A/G]AAGTATTGATGGAGA | 22836 |
| rs2112402 | snp | C/T | | | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95734321 | AAGATGAGTTCAATT[C/T]TCCAAATGTGGCTCC | 22836 |
| rs2302980 | snp | C/G | 0.00161434 | 0.0283648 | missense, utr-variant-5-prime, upstream-variant-2KB | RHOBTB3, SPATA9 | GRCh38.p7 | 5:95731918 | ACCAGGACAACCGGC[C/G]GTCGGGGCTTATCCG | 22836 |
| rs2431341 | snp | A/C | 0.476833 | 0.105105 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95739792 | TCAAGCCATCTGCCC[A/C]CCTCAGTCTCCCAAA | 22836 |
| rs2431342 | snp | A/C | 0.488666 | 0.0744214 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95739970 | TCCCCACACAAATCT[A/C]ACGTTGAATTGTCAT | 22836 |
| rs2431343 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95739973 | ccacacaaatctaac[A/G]ttgaattgtcataat | 22836 |
| rs2431344 | snp | C/T | 0.491316 | 0.0653198 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95744018 | CTGGCCCCTCTCCCC[C/T]TTCCTTCTTTCCTTC | 22836 |
| rs2432034 | snp | C/G | 0.484632 | 0.086302 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95744363 | TCCAAAGCCACCACA[C/G]AACAGAGGAGAGAAA | 22836 |
| rs2545639 | snp | G/T | 0.492918 | 0.0590819 | | | GRCh38.p7 | 5:95735803 | ACTGAAAAATTATAT[G/T]TAAAATATCAACCCA | 22836 |
| rs2548126 | snp | C/G | 0.498568 | 0.0267188 | | | GRCh38.p7 | 5:95738809 | ATAATTGTTATTAAA[C/G]TGTATTAAATTTGGC | 22836 |
| rs2548127 | snp | A/T | 0.498568 | 0.0267188 | | | GRCh38.p7 | 5:95737445 | GCTCCCAAGCCCACA[A/T]CTTCATGTGAACAAT | 22836 |
| rs2548128 | snp | C/T | 0.465892 | 0.126058 | | | GRCh38.p7 | 5:95736128 | CAGTAAGTAATTTAT[C/T]ACAAACACTATTCCT | 22836 |
| rs3072751 | in-del | -/CC | 0.484701 | 0.0861117 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95762589 | GGTCTCCTAACTATA[-/CC]GCCCACACTAGGCTT | 22836 |
| rs3079940 | in-del | -/AAAA | | | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95783585 | aaaaaaaaaaaaaaa[-/AAAA]gaagaagaagaaagg | 22836 |
| rs3184188 | snp | G/T | 0.127254 | 0.217792 | utr-variant-3-prime | RHOBTB3 | GRCh38.p7 | 5:95796053 | ATGAATGAAATTAAT[G/T]CTGTCCAAGCCAGCA | 22836 |
| rs3734133 | snp | A/G | 0.495291 | 0.0482933 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95773527 | CAGACACACTGGTCA[A/G]GACGCAAAGCCAAGG | 22836 |
| rs3756706 | snp | A/G | 0.49566 | 0.0463812 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95790247 | TGACAGCAAGCATAC[A/G]CAAGCCTTATCTTTA | 22836 |
| rs3756707 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95771987 | ATGCAGAAACTGATT[C/T]GATCTCCATAAACTA | 22836 |
| rs3756708 | snp | A/G | 0.365646 | 0.221644 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95766787 | CGTCTGTCCTGTCGC[A/G]CCTGGCTGGAGCTAG | 22836 |
| rs3777212 | snp | A/G | 0.392881 | 0.205147 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95791415 | AACAAACAAAACCCC[A/G]TAACACAGAACACAT | 22836 |
| rs3777213 | snp | C/G | 0.328616 | 0.237317 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95791325 | TTCCTGTGCACCGCT[C/G]TTTGTGTTCATGAGT | 22836 |
| rs3777214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95790912 | TAGCCAGATCTTCCA[A/G]TTTTTCAAAAGAAGC | 22836 |
| rs3777215 | snp | C/T | 0.325799 | 0.238232 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95786296 | GGAGTCTAATTCTGC[C/T]AGAAGACAATTTCAC | 22836 |
| rs3777217 | snp | C/T | 0.464096 | 0.129085 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95780839 | AGTCCTTAAAAGTGC[C/T]CCAATCAGAAGTCAC | 22836 |
| rs3777218 | snp | A/G | 0.498734 | 0.0251279 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95777162 | AACTCTTCATGTGAC[A/G]GACTCATATCAAAAG | 22836 |
| rs3777219 | snp | A/G | 0.495056 | 0.049474 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95764713 | ACAGAAAAGTCATCT[A/G]TATTAAAAAATTAAA | 22836 |
| rs3777220 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95763121 | AAATCTTACCAGTTA[C/T]GGGCAGCAGTGACTA | 22836 |
| rs3806895 | snp | C/G | 0.202651 | 0.245475 | upstream-variant-2KB, intron-variant | RHOBTB3, SPATA9 | GRCh38.p7 | 5:95730592 | TGGCCATAACGTGTA[C/G]AGAAAAATCTCCAAG | 22836 |
| rs3822752 | snp | A/C | 0.253824 | 0.249971 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95791532 | AGCTGCTCAGCTCTA[A/C]GTTTCAAGAGGAAGC | 22836 |
| rs3822753 | snp | A/C | 0.473081 | 0.112848 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95788624 | GATGCAGCTTTCAGT[A/C]TACTGTGACAGCAGA | 22836 |
| rs3822754 | snp | A/C | 0.394354 | 0.204112 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95781511 | CAAAATACTCTACAG[A/C]AAGCTGCAAGCCCAG | 22836 |
| rs3836905 | in-del | -/ACT | 0.48679 | 0.0801892 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95755219 | CAGCGATTTTCTACT[-/ACT]GCTTAACCTAATTTA | 22836 |
| rs3836906 | in-del | -/ACA | 0.496034 | 0.0443518 | intron-variant, upstream-variant-2KB | RHOBTB3, SPATA9 | GRCh38.p7 | 5:95732701 | AAAGTTTTCCAAACA[-/ACA]TTAGTAATGTTATTT | 22836 |
| rs4256370 | snp | G/T | 0 | 0 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95751769 | tgtttagctcccact[G/T]ataagtgagaacatg | 22836 |
| rs5869687 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RHOBTB3, SPATA9 | GRCh38.p7 | 5:95732705 | AACATTACTAATGTT[-/G]TTTGGAAAACTTTTA | 22836 |
| rs5869688 | in-del | -/T | 0 | 0 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95741503 | TTCTCTTTTTTTTTT[-/T]CTTTCTTTCTGTTTT | 22836 |
| rs5869689 | in-del | -/C | 0.485255 | 0.0845871 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95745269 | TTAAAAAGAATTCAG[-/C]CAAGTATAATCCAGT | 22836 |
| rs5869690 | in-del | -/A | 0.0329836 | 0.124112 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95748676 | TTTTCTCTCCAAATG[-/A]AACCTTTTCTATTTA | 22836 |
| rs5869691 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95751539 | ACAATTCCTTCCTTG[-/A]AAAAAAAACTTTTAT | 22836 |
| rs5869692 | in-del | -/AA | | | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95782833 | AAAAAAAAAAAAAAA[-/AA]GGTTAAAATGGTAAA | 22836 |
| rs6556878 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95742955 | gggcgcctgtagtcc[C/T]agctactcgggaggc | 22836 |
| rs6556879 | snp | A/G | 0.485049 | 0.0851591 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95770921 | GCCTACAAATAATTT[A/G]TTTTGTATTTTTGAA | 22836 |
| rs6556880 | snp | A/G | 0.473359 | 0.112298 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95789154 | ATGTGTCCTCAGGTG[A/G]CATTTGGTTGTGAAA | 22836 |
| rs6871987 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95777077 | AATTTGTTGTTTTGG[A/C]GTGTAAAAAAAAATT | 22836 |
| rs6876583 | snp | C/T | 0.491157 | 0.065903 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95761147 | TTTATAGGTGTTTTT[C/T]AGTTAATATGCTTTT | 22836 |
| rs6876866 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95743380 | GCTGCTTCCACTGGG[G/T]TTCTCCCACTCATCC | 22836 |
| rs6885784 | snp | C/G | 0.494568 | 0.0518327 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95767245 | CACTTCATTACTCTA[C/G]GTTATTTTTTTAACT | 22836 |
| rs6890561 | snp | A/G | 0.394538 | 0.203982 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95781741 | TGTAATCCCAGCTAC[A/G]CGGGAGGCAGAGGCA | 22836 |
| rs6894297 | snp | A/G | 0.4862 | 0.0819127 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95764647 | GGTAAGTTATATGCA[A/G]TACTTAGCGGAGTAA | 22836 |
| rs6894714 | snp | C/T | 0.492582 | 0.0604491 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95781601 | CTCATGCCTGTAATC[C/T]GAGCACTTTGGAAGG | 22836 |
| rs7706030 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95747762 | CTCTGAAGTCAAATG[C/T]GTTAGAGTTTAATGA | 22836 |
| rs7714523 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95756330 | caagttgtggcatgt[A/G]tcaggattttcttcc | 22836 |
| rs7716916 | snp | A/G | 0.480064 | 0.0978296 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95761530 | GTATTTTTAGTAGAG[A/G]TAGGGTTTCCCCATG | 22836 |
| rs7717280 | snp | A/C | 0.497803 | 0.033074 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95761793 | GCATAGAGTAATTTT[A/C]TTGATCTGGGATCCA | 22836 |
| rs7723251 | snp | C/G | 0.0433465 | 0.140692 | downstream-variant-500B | RHOBTB3 | GRCh38.p7 | 5:95796810 | GCATGGAATGATGCA[C/G]TCCCTCCCCAGCAGG | 22836 |
| rs7729314 | snp | A/G | 0.490836 | 0.0670685 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95760858 | ATGTTTTTACCACTG[A/G]AAAAATAAAAGGAAA | 22836 |
| rs7735516 | snp | C/T | 0.124144 | 0.21601 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95776802 | GACTTTGTGATGTGG[C/T]CACGGGGGTTGAGAT | 22836 |
| rs7735810 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95776952 | ATCTTTCCTTTAAAG[C/T]GTCCCAGGCCTTCCC | 22836 |
| rs7735816 | snp | C/T | | | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95776964 | AAGTGTCCCAGGCCT[C/T]CCCCCAAAACTGGCT | 22836 |
| rs7736292 | snp | A/T | 0 | 0 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95777281 | TGAAACCAAAAACAG[A/T]TCTAAAAATTTCACT | 22836 |
| rs9314154 | snp | C/T | 0.446641 | 0.154377 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95782453 | atgttctggagatgg[C/T]ggtggtgatgactgc | 22836 |
| rs9314155 | snp | C/T | 0.394904 | 0.203722 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95782534 | ttaaaatgggccgga[C/T]gtggcggctcatgcc | 22836 |
| rs9314156 | snp | C/T | 0.467845 | 0.122652 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95782609 | gtcaggagatcgaga[C/T]catcctggctaacac | 22836 |
| rs9314157 | snp | A/G | 0.330016 | 0.236849 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95783624 | AAAAGATAAAATGGA[A/G]TAAAAGTGCAGAATG | 22836 |
| rs10042637 | snp | C/T | 0.469642 | 0.119404 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95776106 | AATTAGATGATTATC[C/T]ATCTAAATGTAATGT | 22836 |
| rs10046014 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95760251 | ACTAATCCTAAGGAA[C/T]GAGGAGTAATGTGAT | 22836 |
| rs10057261 | snp | C/G | 0.394904 | 0.203722 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95791763 | GTTGGCCAGGCTGGT[C/G]TCAAACTCCTGACCT | 22836 |
| rs10065277 | snp | A/C | 0.329783 | 0.236927 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95783382 | ccacctcggcctccc[A/C]aagtgctgggattac | 22836 |
| rs10076138 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95735615 | TGTTAGTCAGACCTA[A/G]CTATTTTCTTAATCT | 22836 |
| rs10476659 | snp | A/G | 0.395453 | 0.203331 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95782223 | ATGTTATTATGTTAA[A/G]TATTCACCATACACA | 22836 |
| rs10648744 | in-del | -/ACTA | 0.39979 | 0.200158 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95781857 | CCGTCTCAAAAAAAG[-/ACTA]ACTTAGTATTTTTGC | 22836 |
| rs10718378 | in-del | -/T | 0.496968 | 0.0388195 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95735260 | AGTCCATATTTTGCC[-/T]TTTTTTTTTTTTTTT | 22836 |
| rs11135432 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RHOBTB3 | GRCh38.p7 | 5:95777382 | CTTGATAATCTATGT[A/T]AAGTGACTAGAAAAC | 22836 |