SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs139545541 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885434 | TGATGTAGCTGCTTC[C/T]GCTAGACCTAAGTAC | 9886 |
rs139578469 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994958 | AAACAGAGCACATAA[-/T]GAAAGATGCGGCTAA | 9886 |
rs139583359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875246 | GCCACTTCACCCACA[C/T]CTCTGGGGACTCTAG | 9886 |
rs139594113 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989900 | GGGAGAAACAGGTGG[A/G]GCTGTGCTCATACAA | 9886 |
rs139596004 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934422 | CAGCATAGAACAATG[C/T]AACAAGGATACACCT | 9886 |
rs139610947 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906925 | GTGATTCTCACATGT[C/T]GTGATGTCGTGGGAG | 9886 |
rs139622405 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878864 | GGAGATGTACACTGC[A/G]TAGCAGCTACTCTTT | 9886 |
rs139627798 | snp | C/T | 0.000115387 | 0.00759474 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892889 | ACCCAACAAGGATAA[C/T]GGGTGTTCGAGGGCA | 9886 |
rs139661763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985636 | GACTCAAATTCTAAA[C/T]CAGATAAAATATATT | 9886 |
rs139669589 | snp | C/T | 0.000132076 | 0.00812532 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886210 | CACTGATGGCTCCAT[C/T]GTCCAATTTAAATGT | 9886 |
rs139688091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882092 | TAATTAACTGCATGA[C/T]AACAGAAAGACCTTT | 9886 |
rs139723972 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981850 | CCTCGGCTCACTGCA[A/G]CCTCTGCCTCCTGGG | 9886 |
rs139755525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885883 | TGCCCCCACACCAGT[A/G]ACCAATAAACAATAG | 9886 |
rs139770282 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898788 | ATTTTTTTCCAAGCC[C/T]GTATCTGCATGTTTA | 9886 |
rs139777272 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972747 | CTAAGTATGATCATC[A/G]GCTTAGCACACAATA | 9886 |
rs139790817 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889703 | GAAGGATCATCACTT[C/T]ACTAGCTATTTAATC | 9886 |
rs139819881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921382 | GAGAGAAAGGATGGT[A/G]CCTCTGACAGGCAGA | 9886 |
rs139949606 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917110 | AGAACTATAAGAAAA[C/T]AAACTTTGTTTTATG | 9886 |
rs139971013 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904575 | AGCTCTCTCTCTAAT[C/G]GTCAAAAATTCTTCC | 9886 |
rs139978214 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893234 | CAGAATGCTGATGCA[C/T]TGACGTTTCCGATGA | 9886 |
rs140015901 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963214 | ATTTTCATTGCCCTC[C/T]GCTCCATACAGAGAC | 9886 |
rs140018545 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913513 | ATGGTTTTCTTAGTT[A/G]CCCATCTAACAGTAT | 9886 |
rs140018649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967695 | TTTGCATTCTAAATG[C/T]CTTCAGGGGTGAGAG | 9886 |
rs140023332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948048 | TGTAGTGTTACTTTG[C/T]ATTCCCCTAATGAAT | 9886 |
rs140035290 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869633 | TTTGGCAAGATTACA[A/G]TCAAATGGGAGCTTT | 9886 |
rs140044567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894696 | CCACCATGAATTTTG[A/G]TACAGTGAGAATAGA | 9886 |
rs140070457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873972 | GTAAAGTTCAATTCC[A/G]CCTTTTCCCCCTTTT | 9886 |
rs140081209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963069 | CCAAGAAGTATTGCA[A/C]ATATGTATAATTTGC | 9886 |
rs140110035 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898225 | TGTGCATGAGTCCCC[C/T]TCTGGCAAAGATTCA | 9886 |
rs140200854 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926773 | CTGGCAGCTAGTATC[A/G]TACTGAATGAGGAAA | 9886 |
rs140201091 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900533 | AGCTGTCTTTTCCAC[C/T]GTACTATGAGGTCAT | 9886 |
rs140214457 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883049 | GAGCCACTTCCCCAA[C/T]GTCAAGCTGAGAGTA | 9886 |
rs140221717 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970163 | GATTGTTTGCCTGTA[A/G]TAGTTAATAGCAACC | 9886 |
rs140269234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919079 | TCAAGGCATGGTGAG[C/T]AGTCTGCTTAAAGAC | 9886 |
rs140331100 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990445 | CTCAAACAGGCAGGA[A/C/T]GACAGACAGAACCAG | 9886 |
rs140336042 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965129 | ATAGTATGTTAGGGG[C/T]TGTACATATACAAAG | 9886 |
rs140431485 | snp | C/T | 3.29707e-05 | 0.00406008 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888410 | CATCCAGTTGTCCCG[C/T]ATAAAGAAACTGGAG | 9886 |
rs140443769 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936788 | AAGCTTGAGCACAGC[G/T]CTAAAAGCAATTAAT | 9886 |
rs140507695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941513 | TTATCAAGCATCCAG[A/T]TCCCCAGTATTCTCA | 9886 |
rs140546646 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, synonymous-codon | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944515 | ATGGGAGACCCCGGC[C/T]CTTTCCCCGCGCTGC | 9886 |
rs140570952 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987145 | TATCAGTGAAACAAA[C/T]CACAGCATGAGGCCT | 9886 |
rs140579660 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991219 | TTTTCAAAATGTAAA[A/T]TTGATGATGTAACTA | 9886 |
rs140620742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982904 | TCTTCCGCTCCCTTC[C/T]TATGGTGGGCATGGA | 9886 |
rs140624870 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939400 | TTACAAACTAAAAAT[-/A]AAAAAAATTATGATG | 9886 |
rs140647945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880423 | ACACCTCAGAGAGGG[A/C]ATATCCTTTCAGATA | 9886 |
rs140673515 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888899 | TGTCCAGTAAACAGG[C/G]AGCTTCATTTGTCCC | 9886 |
rs140680736 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883585 | AAGGGGAGCAATCCT[A/C]CCAGCTCTTTATCTC | 9886 |
rs140738374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879225 | TCTGCGGTGCTGGAA[A/G]TGTTTAATGCCAAGG | 9886 |
rs140750129 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995506 | TTTATCTTACTGTTT[A/G]AAAGGCTTTGGGGAA | 9886 |
rs140756139 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910162 | TAAAAAAAAAGTCTC[C/T]ATTAATACAGAATTT | 9886 |
rs140785192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962435 | TTTACAGGTTTGTCT[C/T]AAATTGCAAATGCAA | 9886 |
rs140787698 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906804 | GAAATTTTATAGGGG[-/A]AAAAAAAAACAATAA | 9886 |
rs140793094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923060 | TGGGATGCTATCATA[C/G]AGCCCTACCTTGATC | 9886 |
rs140825971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973628 | AACACAGAAGGCCCA[G/T]GAAGCAATACTAGAC | 9886 |
rs140860536 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964500 | CTTAAAAACTTTACA[C/T]TGCATGCTTTTCTAA | 9886 |
rs140919011 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890737 | GAATTTGGATTTGAC[G/T]ACTTAGATGAAAAGG | 9886 |
rs140929657 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960910 | GCAGGATTGTGGTCA[C/T]TGTCAAACTCTCCCC | 9886 |
rs140930174 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982060 | ACAGGCATGAGCCAC[A/T]GTGGCTGGCCTGTAA | 9886 |
rs140977970 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896407 | CTCAGGGGTCCTGTT[C/T]CAGCTGTAAAAGAAT | 9886 |
rs140981074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999229 | CTATTTAGCAACTGC[A/G]CATCCAAATTTTAGT | 9886 |
rs141045759 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900283 | AAGAGGTAAGAATTC[C/T]GAGAGAGAGGATGGT | 9886 |
rs141075488 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949197 | TTCCTGCTAAAGTAG[A/G]TGCTTCTCCAAGGTG | 9886 |
rs141080412 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914176 | GATCTTAAGCAAAGA[A/G]GACAGAAAAAGTTTT | 9886 |
rs141107533 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991592 | CATGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 9886 |
rs141139124 | snp | C/T | 0.000198203 | 0.009953 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892850 | TAACAGCTTCCAGGT[C/T]GGCATAGCGGAGATC | 9886 |
rs141225534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875673 | TGCGTACGTCTGTCT[C/T]AACAGCTACAGATGG | 9886 |
rs141244168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888037 | ACAATCATATTTAAC[C/T]TTTAAGTCTGATGAG | 9886 |
rs141249035 | snp | A/C | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946197 | AAAAAAAAAACAAAA[A/C]ACTGACTTCCCTTAG | 9886 |
rs141277822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942977 | CTGGCTGGAGTTCAA[C/G]AAGGCTCAGTGAACA | 9886 |
rs141290418 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992319 | TTATGATATAAGATG[C/T]GTGCTAAGATATGAA | 9886 |
rs141310719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937281 | GTGCTGCAGATGAAA[C/T]GGGGAAATTGTGGTG | 9886 |
rs141310783 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991024 | ATAGATATCACAGAA[C/G]GTGGCCTGTCAATTT | 9886 |
rs141327585 | in-del | -/GGGGAACCTTCTTTAT | 0.0310518 | 0.120672 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955346 | ACACCCAGCCAGCAA[-/GGGGAACCTTCTTTAT]GGTTTTAAAATGCCA | 9886 |
rs141330225 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927968 | GAATATATGAGCAGC[A/T]CAAACAACTCAACAG | 9886 |
rs141342559 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987415 | GTGGCACTGCCACTC[C/T]CCCTGGTTCAACACT | 9886 |
rs141354242 | in-del | -/GAAA | 0.00358994 | 0.0422147 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918387 | CTGTCCCTCTCTTAT[-/GAAA]GAGACTCCCAGGAAG | 9886 |
rs141397467 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923426 | TATAAGGTCACCAAA[A/T]TGAAAGCCGTGCTGG | 9886 |
rs141425241 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880078 | GATCTATGCAAATAC[A/G]ATGCCATTTTATATG | 9886 |
rs141437380 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998041 | AGGTATTGTCTAGAC[C/T]TAAATTTCTATTATC | 9886 |
rs141462265 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974931 | TATAAGCAAATGTGA[A/C]TAAGAAATGACTCAT | 9886 |
rs141467261 | snp | A/G | 4.96956e-05 | 0.00498451 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888503 | TCCGCTTTGAAATGG[A/G]GTTGACTTGCATTTC | 9886 |
rs141476055 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903144 | GGAATTCTAGGAGTA[C/G]GTGACACTTGTTCTA | 9886 |
rs141479980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925738 | AGATGTTACAACTGA[C/T]ACTGCTGAAATTCAA | 9886 |
rs141513070 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975784 | TAACAGAATAATATA[C/T]ACAAAGATGACCAAT | 9886 |
rs141531628 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970893 | CCTTGTAAAAATATT[A/C]ATGGAGAGTCAAACT | 9886 |
rs141543062 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967305 | TTTTTTTTTTTTTTT[C/T]TTTTTTAGACAGAGT | 9886 |
rs141577627 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872819 | GAGAGATCCAGATAC[C/T]CCACCCTTCCATTCT | 9886 |
rs141580500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887005 | AATTAAAAATAATTC[C/T]CTATTATCATCCACT | 9886 |
rs141618901 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984041 | ATACCACTTAAAATC[C/T]CTCTAACTTTCTGAA | 9886 |
rs141622630 | snp | A/C/T | 0.000230645 | 0.0107368 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888956 | TGACCGGTGGAGGGG[A/C/T]TTTTGGAGGTAGGAA | 9886 |
rs141644180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890400 | TAACTTCCTCTGATG[C/T]CACAAAGCCCCTGGA | 9886 |
rs141687013 | snp | A/G | 6.60895e-05 | 0.00574808 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874962 | TACAAACCTGAGCCA[A/G]TTCCAAGTAAGAGAG | 9886 |
rs141735163 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911238 | CGTGGCACTAAAAAG[G/T]TTAGTTTTGTTTTGA | 9886 |
rs141764595 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915816 | CCACTCCTCCACACT[C/G]CCTGCCCACACAGCG | 9886 |
rs141798179 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966144 | ATGTCTTGAAAAGAT[G/T]GAGATGTTTGCAAAA | 9886 |
rs141800442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961408 | GGGGCAAATAACACC[A/G]GTGCATTAAGTATAC | 9886 |
rs141817738 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958759 | GTGTGCACCACCATG[C/T]CCAGTAAATTTTTGT | 9886 |
rs141860044 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881224 | TCCCAAGCCATGTGG[A/G]ACTGTGAGTCCATTA | 9886 |
rs141866662 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957023 | GAAGTATTTTTCACT[C/T]AAACATTTTGCTATA | 9886 |
rs141885770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955312 | TCCCAAAGTGCTGGG[A/G]TTACAGGCATGAACC | 9886 |
rs141897322 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869174 | GTTTCTCCCCCAACC[C/T]GCTCTCTGGCCCCAG | 9886 |
rs141901044 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971286 | ATCACGCTACCTGAC[C/T]TCAAACCATACTACA | 9886 |
rs141908851 | in-del | -/G | 0.0236746 | 0.106192 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945770 | AGTATTTTTGAAAAT[-/G]GGAGTTACCAAGGCC | 9886 |
rs141934242 | snp | A/G | 0.000312966 | 0.0125054 | synonymous-codon, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872257 | TGCAGATGTGGTGCA[A/G]ACACCAGGCGGCCAA | 9886 |
rs141948975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950040 | ATTTTGCAAATTCTG[A/C]AACTCTAACTGCAGT | 9886 |
rs141990375 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874131 | AGACTTAGTAAGTCA[C/T]TGTCTTAACAGAAAG | 9886 |
rs141997936 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905048 | TATCTATTTATAAAG[C/T]CTGCCATTAGGGCCA | 9886 |
rs142047266 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877775 | AATTTGATTAATTCA[C/T]ATCATTCTACACAAG | 9886 |
rs142064660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908692 | AACTTTTTGGCATTA[C/T]GTCAATGTGATATTA | 9886 |
rs142087713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882782 | TAACCACCTGTATTG[C/T]ACTTTCCTAGTTCAG | 9886 |
rs142119586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927734 | TAGATTAAATACTTA[C/T]ATCTAAGACCTCAAA | 9886 |
rs142224754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936424 | TTTATGTCAATTTGC[A/G]TATGCACATACATGC | 9886 |
rs142229647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907383 | CCTTTAAGAAGAGGC[A/G]CTTTCCTTGCCAAAA | 9886 |
rs142235548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936423 | ATTTATGTCAATTTG[C/T]GTATGCACATACATG | 9886 |
rs142258251 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986941 | CAACAGTAAGGAGGA[A/G/T]TTTCTGAAGGAAATT | 9886 |
rs142263901 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933739 | TCATCATATCACTAT[C/T]TGTGGAAACAAAAAT | 9886 |
rs142299445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913233 | ACGCCATCACAGGAG[G/T]TGTTAAAGCTGAGGC | 9886 |
rs142302839 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930203 | AAACAACCTATGACA[A/G]GTGAGGGAATGATTA | 9886 |
rs142387224 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991174 | CTTCCCCCTTGCCAA[C/T]CCATATTCCACACGG | 9886 |
rs142395561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890150 | ACTTTCCCACTTCTA[A/G]TTAAATGATCCACTT | 9886 |
rs142400059 | snp | C/T | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888895 | GGATTGTCCAGTAAA[C/T]AGGCAGCTTCATTTG | 9886 |
rs142429110 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918692 | CCATTGGAATATGCT[G/T]CATCTTATCACTTAC | 9886 |
rs142462833 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968685 | CTCAAATAAACCATT[G/T]TGAGACTGACAGCCG | 9886 |
rs142465294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892129 | TCAGTCTCAATTATC[C/T]CTTTATTAGCAGCAT | 9886 |
rs142544361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955970 | AAATATCACAGTGGG[C/T]CTCATTTGTTAATAG | 9886 |
rs142613153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951453 | TTATGCCTACTTTAA[C/T]ACTTCACATGACCTA | 9886 |
rs142654923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994663 | TTATTATACATTAAA[G/T]TCATTCAATAAATAT | 9886 |
rs142659179 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909201 | AAATAAATGCTATGC[A/T]GGAATCTCACAAGAT | 9886 |
rs142676215 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997705 | GGCTGCTTGATGGAT[C/T]ATTAAAATAGTAAAT | 9886 |
rs142696661 | in-del | -/TTTAT | 0.477768 | 0.103061 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990502 | ACTTAGCAATTTCTC[-/TTTAT]TTTAATTCAAAAATA | 9886 |
rs142704691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875124 | GGGTTGGTCTGGGAC[A/G]ACTTAAGAAGGGAGG | 9886 |
rs142757231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985266 | TTCAAATAATTCTAC[A/G]TTTTTTAGGCACAAT | 9886 |
rs142770925 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942304 | ATAGCTTATAATTTG[C/T]ATTATTGAGCCAATA | 9886 |
rs142812595 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907108 | TTTGCTCCTCCTTTG[C/T]CTTCTGCCATGATTG | 9886 |
rs142829911 | in-del | -/C/CG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886717 | TTTTTTAAGAGATGT[-/C/CG]GGGGGGGGGTGGGTC | 9886 |
rs142840609 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957258 | ATCCTTATCAAATAC[C/T]ATGTGCTGTACCTAA | 9886 |
rs142844286 | snp | A/C | 0.000164859 | 0.00907756 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889123 | TCATAGTATGGTAAG[A/C]CAAGTTCCTTTGCTA | 9886 |
rs142902743 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881965 | AACAACATTAGGGAC[A/C]TTTAGAAAAAAACAT | 9886 |
rs142942093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994295 | AATGAAATAATCAAA[C/T]GGTAGTATACTACAA | 9886 |
rs142943666 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931750 | AACCTGTTTCTTTCT[C/G]TGACTCAAGCTCTCA | 9886 |
rs142946112 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963099 | CAACCAAAGCAATCT[G/T]CATAAACAAGTGATC | 9886 |
rs142950407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885945 | GACCAAACCCTCAAG[C/T]ACTACTAAGGAGCAA | 9886 |
rs142969147 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884260 | ACAATGGGAGTGCTC[C/G]AATTTCTTGTGCTAG | 9886 |
rs143005753 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988620 | CTGCATTCACATTGT[C/T]GCAAGGGACATGATT | 9886 |
rs143010264 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926711 | TTCCCAAAAACCTGG[G/T]TATGGAAGGAACATA | 9886 |
rs143010364 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983339 | TAAATAACAATTAAC[C/T]GAATGAAATTTGCTT | 9886 |
rs143048611 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914982 | ACTTGCTCCAGATGT[C/G]GAATTTCCAGGAAGC | 9886 |
rs143055291 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967334 | GTCTCACTCTGTTGC[A/C]CAGGCTGGAGTGCAA | 9886 |
rs143074412 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977909 | GCATGATGAAGTTCA[C/T]GTAGACATAAATTAA | 9886 |
rs143090166 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871390 | TGAACTATGTCGTAT[C/T]TCTAACAAGACGAAT | 9886 |
rs143138135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972959 | TGTCGAAAGCAAGAA[C/T]GATTTTAGTTTGAAA | 9886 |
rs143140056 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918834 | CACCACAAACCTCCA[A/C]CTCCTGGGTTCAAGC | 9886 |
rs143150912 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920718 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCC | 9886 |
rs143164372 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887853 | GATAGGCTTGGGGTC[C/T]CTGATCCACTCTTGA | 9886 |
rs143184615 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970688 | CAAATACTTTTTAAC[A/G]GTTCCGTGGTCAGAA | 9886 |
rs143209310 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969817 | TTTGGATCACTTTTA[C/G]GCTATGCTTTTAGTA | 9886 |
rs143267970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883994 | CTCAGGAGAGATTTT[C/T]ATTAGTCACAGGTGA | 9886 |
rs143287647 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975335 | ATGGTCCAGAGACTT[C/G]TGTTCCTGGCCCAGA | 9886 |
rs143326171 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898031 | ATTTACCCAAGTTCT[A/G]CTTGAAGTATCTCCT | 9886 |
rs143389789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983809 | TGCCTTGCTACACAG[A/C]ATGGACCCTGCAGAG | 9886 |
rs143431721 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909788 | GGGGACATTAAAATC[G/T]TGTTTTGCTTCCATA | 9886 |
rs143435198 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904788 | ACCTAACCTCTTAGG[A/G]AACAACTATTTCTAT | 9886 |
rs143464268 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960435 | ACTACTCACACAAAC[A/C]AAATGGCCCCTTAGA | 9886 |
rs143473043 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945808 | TTGATATCAGAAAGA[A/G]AGGGTAGTGAAAAGT | 9886 |
rs143510746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904854 | TTCTACTTTTTTCTA[C/T]AACCTGAGCAATTTT | 9886 |
rs143565010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953086 | GTCAGGTTGATGAGA[C/T]AAAATGGGAAAGTCA | 9886 |
rs143565088 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869991 | TCTCATTTCCATCTT[A/C]TGAAAAGCTAGAAGA | 9886 |
rs143605773 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989963 | CCAATTCAGACCTCA[A/G]AACCTCAGAATGTCC | 9886 |
rs143633723 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948158 | GCCTATTTTATAATT[A/G]GATTGTCTGTCTTTT | 9886 |
rs143671758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884538 | GAGGCTGTACTCCCA[A/T]GTTAACTGTAGCACT | 9886 |
rs143710312 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931399 | TCTACAGATTTTCCT[A/C]TTCTGGACACTTCAT | 9886 |
rs143748416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948680 | CAGGGGTTTGAAGCA[C/T]GAAAGAGAATAAGCT | 9886 |
rs143799442 | snp | C/T | 0.00037941 | 0.0137681 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871579 | CGTTCCCTTTTCACA[C/T]GCTGGTAGTGATCTT | 9886 |
rs143817674 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938891 | TGTAATTTAGTTAAC[A/G]TGTTTGGCATCTAGT | 9886 |
rs143825190 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924447 | CAAAGGGGTCAATTA[A/C]GCAAGAGGATATAGC | 9886 |
rs143857492 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966305 | TTCTGATTATATTCG[-/A]AAAAAAAAAAAAGCA | 9886 |
rs143884652 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927710 | CTGTATACAAAAATT[A/G]AATCAAAATAGATTA | 9886 |
rs143889401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921237 | ACCAGCATGAGCCAC[C/T]ATGCCTGATCCTGAT | 9886 |
rs143920514 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883058 | CCCCAACGTCAAGCT[C/G]AGAGTATATTATAGT | 9886 |
rs143923110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917741 | ATTGGGGGAGGGGGC[A/C]GACATTCACCCTGTA | 9886 |
rs143944348 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980483 | AAACAATTGTCTATT[A/G]TGACATTGAGATGCT | 9886 |
rs143971474 | snp | A/G | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882432 | GAGTACCTCTGGGGA[A/G]AGAATTATGCTTACT | 9886 |
rs143978611 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926812 | GCCTTTTTTCTAAGA[C/T]CTGGAAGAAGACTAG | 9886 |
rs143979338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885731 | CTTTCTGAACTACTG[A/G]GAGACATGCTCCTCT | 9886 |
rs143993186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991957 | AGTCCATAGGCTAAA[C/T]GGAGGCAGAGAGTAT | 9886 |
rs144012256 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922556 | CATGTCCACGGGGAA[A/G]AGAATTGGCCCAGGA | 9886 |
rs144102748 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905765 | TACAATGTTATTTCT[G/T]GCCCAGGCTTTAGAA | 9886 |
rs144160978 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899563 | GACAAAAGGACTCTA[C/G]CCAGCCTCCTTGGCA | 9886 |
rs144177505 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878152 | ATATCCTGTGTGACT[C/T]GATATTGGTGAGTGT | 9886 |
rs144188870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992896 | CCACAAATCCACATA[A/G]TGTTCTAAAGAAGCC | 9886 |
rs144194034 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903782 | TGACAGTGTCCCATC[A/G]TTAGTTTCAGGGTTA | 9886 |
rs144247249 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962361 | ATATGCCCAATGACT[A/G]ATAAATACAAGTGCG | 9886 |
rs144262692 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873102 | AGAAAAGCCAGAGAC[C/T]TCAGAAACCCACTCA | 9886 |
rs144338589 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902394 | TCTACTTAATGCTCT[C/T]ATCTTTAGGCAAATG | 9886 |
rs144349163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968402 | TGTTTTAAAACAGGA[A/G]TATGAGCACCAAAAT | 9886 |
rs144384027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981037 | AATTTTGGAAATCTG[C/T]CATTTCCTTAAAAAT | 9886 |
rs144391630 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875334 | TAACTCCTGGCCACA[C/T]GAGACTATTTAAACT | 9886 |
rs144457620 | in-del | -/ATAAG | 0.0618563 | 0.164627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952103 | CATGATAAAACTTTT[-/ATAAG]ATGAGTTAGTTATAA | 9886 |
rs144460027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878546 | CGAAATTCTGTCAGT[A/G]TATGCACAATATATT | 9886 |
rs144479065 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885704 | ACTTAGGTGGCTGAA[A/G]AACTCTTTTCCCTTT | 9886 |
rs144485944 | in-del | -/AAAAATTAG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951904 | TCTACTAAAAATACA[-/AAAAATTAG]CCGGGCATGCTGGCA | 9886 |
rs144490751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934296 | CAGTCCTGAGCAGAC[A/G]TCCCACTCATCAATA | 9886 |
rs144527708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951266 | TGGAAGGAGACCTAC[C/T]CATCAGTTCTTGGAA | 9886 |
rs144652110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990263 | GCTGGGATTACAGGC[A/G]TCAGCCACCGTGCCC | 9886 |
rs144656305 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957216 | AAAAGGATAGTCAAC[A/C]CATAACCAGTAATAG | 9886 |
rs144675679 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964742 | TGAAGTTAGTTTGTA[C/T]AGAGAAAAATATGCG | 9886 |
rs144676711 | snp | A/G/T | 0.00183901 | 0.0302683 | missense, synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886229 | CAATTTAAATGTCAC[A/G/T]TCTGCCAAGGGATTG | 9886 |
rs144702353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896811 | TTTGACTAGTCAAAT[A/C]AAAAACAATCTGAAA | 9886 |
rs144720923 | snp | C/T | 0.000132229 | 0.00813001 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911378 | GCGGTACTGGTCAAT[C/T]GCCCACACTGTTGGC | 9886 |
rs144742730 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961234 | CCTTGTGAACATATA[G/T]GAAACCTTGTATTCA | 9886 |
rs144750777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906901 | CCCAAATCTCGAATC[A/G]TAGCTCCCGTGATTC | 9886 |
rs144767483 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900359 | GCATTCTGTATACAC[A/G]CACTGAAGGTATAGC | 9886 |
rs144783545 | snp | C/T | 0.00914312 | 0.0669923 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60868941 | TGTCACTCAGAAAAG[C/T]CCCTCAATGACATCT | 9886 |
rs144799101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958639 | AAAGGGGTCTCACTC[A/G]GTTGCCCATGCTGGA | 9886 |
rs144800687 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921647 | GCAGCTTTCAATAAA[C/T]GTTTGTTGAATTGAA | 9886 |
rs144868333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914680 | CGGAATGGCTGTGTC[A/G]CTTTCACTGAAGATT | 9886 |
rs144925063 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999296 | AGTGTCAAAAAAAAG[A/G]CATCCCCAACTTCAT | 9886 |
rs144970999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908286 | GCAAGGTCTAAAACA[C/T]GTTGGTTTAAATCTG | 9886 |
rs144974860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919393 | GCCAAGTTTCGATTG[C/T]GCAGATTTCATTATT | 9886 |
rs145003562 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871015 | CTCTAATTACGTAAT[A/G]ATGCTCGGTGGTCAT | 9886 |
rs145007854 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970554 | ATTTACCTGAGGAAC[C/T]AATAAATTTTTGATA | 9886 |
rs145049308 | in-del | -/A | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant, frameshift-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945031 | TTCCAGGCTGACCGT[-/A]GAGTTCTGAGGACAG | 9886 |
rs145074817 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986870 | CATCCAGCTCTCCTC[C/T]CTTTCTGTGCCTCTC | 9886 |
rs145091591 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937976 | TGTTCCCATTTTACA[G/T]TTGAGGAAAGTAAGG | 9886 |
rs145106523 | snp | C/T | 0.00166567 | 0.0288108 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888613 | AGAGCCTCCACCAGG[C/T]TCTTGTTTGAAGACT | 9886 |
rs145125995 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872265 | TGGTGCAAACACCAG[A/G]CGGCCAACTGGTGGG | 9886 |
rs145211939 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934974 | ATAGAGAAGGCAGTC[A/G]AGATTGGCTGCTCAT | 9886 |
rs145212114 | snp | C/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882387 | TTGCTTACTACAACC[C/T]AGGCATGCATTTTTA | 9886 |
rs145266138 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986726 | TAATATAAAAACTGA[A/G]GGGCAAAACAGTACT | 9886 |
rs145267043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928740 | ACTATAGTAAATTAA[C/G]AATAATTTATTGTAT | 9886 |
rs145295246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954251 | CCAGTTTCCTCCTCT[A/G]TAAAATGAAAGTGCT | 9886 |
rs145298997 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982022 | GTGATCCACTGGCCT[C/T]GGCCTCCCAAAGGGC | 9886 |
rs145354581 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919093 | GCAGTCTGCTTAAAG[A/C]CAAAAATTGAAGGCC | 9886 |
rs145392206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889843 | ATTAGCATGGCAATG[C/T]TAAGCATAGTATTTT | 9886 |
rs145411431 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002256 | TTTGCTGTGCACCAA[C/G]CTCTAAGTGTGGCCA | 9886 |
rs145420918 | in-del | -/CCA | 0.355096 | 0.226837 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881016 | TAGCTCCCATAATTC[-/CCA]CGTGTTGTGGGAGAG | 9886 |
rs145421331 | snp | A/C/G | 0.00716521 | 0.0594565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915315 | CTGATTTTTATTTAC[A/C/G]TAGAATGAGAGTAAT | 9886 |
rs145430876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879805 | GCACTTGCACACAAA[C/T]ACACACACACACTCA | 9886 |
rs145434749 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959519 | GCAGCAGTGCTAGTG[A/G]ATGTTGCTCACATGT | 9886 |
rs145447135 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891834 | TCTCATCTTGAATTA[C/T]AGTTCCCATAATCCC | 9886 |
rs145466998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894980 | GTTACCATGATAACA[C/T]TCATGGTATTGAACA | 9886 |
rs145480285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997200 | CACTGAGTTCCTCCC[A/G]AAATATCTTTTTTAA | 9886 |
rs145524139 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998566 | TCAGAAGAAGACTCC[C/T]AGAGGAAGTGCAATT | 9886 |
rs145532666 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913754 | GGCTGAGGTTGTGAA[A/G]CCCTGCCTTAGAAGG | 9886 |
rs145534463 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898591 | AGGCCTGTAGGGGAG[C/T]GCCTGGCAGGGGATC | 9886 |
rs145570391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904820 | TCTTGGTTCAAATTG[C/T]TGCTTTTCTTTCATG | 9886 |
rs145574316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923406 | AAGACCAAGTACAAA[C/T]GAAATATAAGGTCAC | 9886 |
rs145667198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958895 | TGTGAGGCACCGCAC[C/T]TGGCCCAGAGTAGGA | 9886 |
rs145680859 | snp | C/T | 4.94531e-05 | 0.00497234 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871564 | ATATCTTCCTTCTCT[C/T]GTTCCCTTTTCACAC | 9886 |
rs145692976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987252 | CTTCTTCTGGCTTCT[C/T]TTCTGCCTTCCCTTA | 9886 |
rs145713599 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899269 | GAATGCAGGAGGCAC[C/T]GAAGTAAAGAAGGCT | 9886 |
rs145734985 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955441 | ATAACAAAAAAATGC[C/T]GTACAGACATGGATC | 9886 |
rs145749657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982410 | TAAGATTTTTGAGGG[C/T]GTATTGTGTATCAGG | 9886 |
rs145756499 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982936 | CAGTGGGAGGGAAAG[G/T]CGGTGCACATGACAT | 9886 |
rs145761338 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905317 | TAGCTGGGTGTGGTG[A/G]TGGGCACCTGTAATC | 9886 |
rs145769386 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894408 | AATAAAGATATCAAG[-/A]TTTTTGGATGCTGGG | 9886 |
rs145786265 | snp | A/T | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 10:60993843 | ATTACTGTAAAAATA[A/T]GAGCATTAAAATTTA | 9886 |
rs145800355 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950735 | CATAAGTGTAAAAAC[A/G]GGCTCATTATGAGGC | 9886 |
rs145940073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889364 | AGTTATGATTGAAGG[A/C]AAAAATAATGCTTTC | 9886 |
rs145958919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892534 | TAATACTTTATACTT[C/T]TCAAAGTGCTTTTAA | 9886 |
rs146008665 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956140 | TATATGGTATAGCCC[A/G]TTGTTTCTAGGCTGC | 9886 |
rs146132472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932148 | ACAAACACATAAATA[G/T]TGATGTACACTCAGT | 9886 |
rs146151580 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926744 | TCAACACAATAAAAG[C/T]AATATACAACAGACT | 9886 |
rs146170609 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978231 | TCTTCAGAATTCTGC[A/G]AAGCATCACAGAAGT | 9886 |
rs146188212 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973140 | CAATATGGACTGCCT[C/G]AAATATAAAGGTAAG | 9886 |
rs146213407 | snp | A/C/G | 0.000313686 | 0.0125199 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874999 | TCCGTCAATGCCCAC[A/C/G]CCACTCGTGGCGGCT | 9886 |
rs146252640 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911653 | TTCGTCCAGCCACTT[A/C]CTTGGAGGTGCACAA | 9886 |
rs146269479 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992369 | ATTATCTTCATTTTC[A/G]CTACTGTATATATTG | 9886 |
rs146301640 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874143 | TCATTGTCTTAACAG[A/C]AAGAGGGAGCACAGG | 9886 |
rs146321185 | snp | C/G/T | 0.00330135 | 0.0404952 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877881 | AAATATGACAGACAC[C/G/T]GCATGGCCCTGAGTC | 9886 |
rs146356306 | snp | C/T | 9.88777e-05 | 0.00703058 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871531 | CACTTTCGTCTTGAG[C/T]GATGCTTATTTAGTG | 9886 |
rs146390849 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972533 | CACACTGGGGCCTGT[C/T]GGGGCATGGGGGGCT | 9886 |
rs146408725 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969071 | TTAGGATTTCACTTA[C/G]TGAGTAAGTGAGATG | 9886 |
rs146428388 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964318 | CAACTGATTATAAAC[A/G/T]CTCTCCTGGGTTTTG | 9886 |
rs146434511 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925011 | GAATGGCTTGAGCCA[A/T]CCTCTTGGTGATAAG | 9886 |
rs146510922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899980 | GGAATCAGTATGCCA[A/G]TATCTGGGGGAAGAA | 9886 |
rs146529631 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904226 | TGCTGGGATTATAGG[C/T]ATGAGCCATTGCACC | 9886 |
rs146533982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947833 | CATAAGTTTTTATTT[A/C]TGTGGGATGAATACT | 9886 |
rs146552574 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942907 | GCAGAACGTACACCA[C/T]CGCAGCGGTTGGGGG | 9886 |
rs146571210 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990961 | GCATCTGTTTTCACA[C/T]ACATGTTCCTCCACC | 9886 |
rs146652230 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922338 | TAGCTGCACTTCAAG[G/T]CAAGATGGCAATGAA | 9886 |
rs146671682 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918871 | CCTGACTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 9886 |
rs146690498 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969845 | GTATTTAAAGAAATA[A/G]AATAATAATACCTTG | 9886 |
rs146709645 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964754 | GTATAGAGAAAAATA[C/T]GCGAAAATTTCCAAA | 9886 |
rs146767091 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870209 | CCTCACGAAAGCTCC[C/T]CTGCTGTCACACTTC | 9886 |
rs146811341 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948169 | AATTGGATTGTCTGT[C/G]TTTTTACTGTTGAGT | 9886 |
rs146831242 | snp | C/T | 0.0944967 | 0.195752 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943911 | CCGGGGCGGTGGGGG[C/T]TCCGCAGCGGCTGCT | 9886 |
rs146841322 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993774 | CATTTATAGGTAGTC[-/T]TTTTTTTTTTCCTCT | 9886 |
rs146849672 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001044 | CCCCCGCCTCCGCCA[-/GT]GTGTGTGTGTGTGTG | 9886 |
rs146871240 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883109 | AGGGACGGGAAGGGG[A/C/T]GAGAATGTCGACAGC | 9886 |
rs146889727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885852 | GAAAAGATATATGGC[A/G]TGTAAAGCACCCAGG | 9886 |
rs146921881 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945275 | GTTCAGCTACCGAGA[G/T]GAATGAATATATTCA | 9886 |
rs146921892 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995031 | CCATGGCTTGGAAAA[C/T]GGTTTAAACAACCCT | 9886 |
rs146928454 | snp | A/G | 0.00169781 | 0.0290864 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872167 | AGCTGGATGAATGGG[A/G]GCCTCACACAGTCTC | 9886 |
rs146938055 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991612 | ATTTTTGTATTTTTT[A/T]AGTAGAGACGGGGTT | 9886 |
rs146944898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875757 | GAAGTAACAAAAATG[C/T]AGTAGGAAGAGCCAT | 9886 |
rs147011229 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923814 | TTCTGCTTTCACTTG[G/T]ATCTCATTTTTTTCC | 9886 |
rs147017635 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884299 | GTGAAAAGTTAGCTA[A/C/T]TGTTTTTTGCATTTC | 9886 |
rs147027250 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975233 | GGGTTCAGAATCAGG[A/G]GAATTCGTCAGAATG | 9886 |
rs147044318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970988 | AGAGAACTTTTGTGA[C/T]GATTCAGTGAAAATC | 9886 |
rs147050633 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890516 | GATGCAGTACAGTGC[C/T]GGGGTTATGGCATAA | 9886 |
rs147122180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901323 | AAATTACTGGTAGAA[C/T]TGTTGTTAAGATTCA | 9886 |
rs147165084 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945811 | ATATCAGAAAGAGAG[A/G]GTAGTGAAAAGTCAA | 9886 |
rs147181899 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940975 | CCAGAGACCCCACAA[C/T]AAAAACTTTCTTATA | 9886 |
rs147271759 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921319 | AACATGTCATGAGGG[A/C]AGGGGTGCAATGGCA | 9886 |
rs147282517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60898696 | GTGAGGCTTCTTAAG[C/T]ACAGATGTTATGTGG | 9886 |
rs147288493 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918326 | CTTCCTTTGGTGGTA[C/T]CCCAACCCAACCTTC | 9886 |
rs147375832 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988892 | CTTCCTATGAAAGTC[A/G]CATTTATAGTACTCT | 9886 |
rs147392718 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985335 | AAAAGCTGATTTTAC[A/T]CACTTGGGATGACTC | 9886 |
rs147405297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878681 | AGGACTCCTTGCTTG[A/G]GACTTCCAGGGGAGT | 9886 |
rs147417532 | snp | C/T | 4.9525e-05 | 0.00497595 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886209 | GCACTGATGGCTCCA[C/T]CGTCCAATTTAAATG | 9886 |
rs147421925 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882055 | TTTTTAAAAAAGCCC[A/G]TTTCTGTGATTTCAA | 9886 |
rs147423566 | in-del | -/AGAA | 0.0869089 | 0.189476 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870252 | TGAAAACTCAGAATG[-/AGAA]AGAGTCAGAACGAAC | 9886 |
rs147428573 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940236 | CAGCACATTAAAAAA[C/G]ATGATATCCTAAGGT | 9886 |
rs147434029 | snp | C/T | 0.000135197 | 0.00822071 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892818 | GGCTTACCTTGCTAA[C/T]GGGCGCCTGGCTCGA | 9886 |
rs147465147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917103 | GATTTTCAGAACTAT[A/C]AGAAAATAAACTTTG | 9886 |
rs147481682 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913371 | CAGATACCTGTCCAC[C/T]TGACACATACTTATC | 9886 |
rs147502919 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897832 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 9886 |
rs147527988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898216 | CTTTGTCACTGTGCA[C/T]GAGTCCCCCTCTGGC | 9886 |
rs147564635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875817 | CCAAGCTGAATTTAC[A/G]TTCTGGTCTGAAGCT | 9886 |
rs147620687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935561 | TTGAGGTATTTCAGT[A/G]TAAAGCAAGGTTGGG | 9886 |
rs147637148 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930021 | TCTGGCTGCAAAGAA[A/G]TAAATGAAACAATTG | 9886 |
rs147670503 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890736 | AGAATTTGGATTTGA[C/T]GACTTAGATGAAAAG | 9886 |
rs147686820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895427 | TTTATTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT | 9886 |
rs147725521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914003 | GACGAATGTCTTCAG[A/G]TGACAACAAAATTGA | 9886 |
rs147739388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994548 | TCCATAATACTTCAG[C/T]CTTGAAATATCTGCA | 9886 |
rs147766749 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914486 | TATTTATTTATTTTT[-/G]ATAGATAAATGTCAT | 9886 |
rs147791365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871802 | AAAAGGTGACACTAA[C/T]GTTCTGAGAGGAAGA | 9886 |
rs147808298 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875397 | TCAGCTCCTCATTCA[C/T]GCTAGCCACAGTAAG | 9886 |
rs147828452 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981284 | AATTACTTTAGGGTC[A/T]AAATAATAAAGATGA | 9886 |
rs147845133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974884 | GGTAGAGAAGGCATC[A/G]TGATGGCATGTATGG | 9886 |
rs147897743 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886447 | CACACATAAAGTCAC[A/G]GCACAAACTCTCTGA | 9886 |
rs147906688 | in-del | -/TTT | 0.283947 | 0.247685 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949665 | GTTTCCAGGTGAAGC[-/TTT]TTTTTTTTTTTTTTT | 9886 |
rs147935328 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958730 | CTGAGTCTCCTGAGT[A/C]GCTGGGATTACAGGT | 9886 |
rs147968799 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999624 | AATTAATCCAAGTAG[A/G]TATACAGATTTTCTT | 9886 |
rs147985775 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910099 | AACAAGGCCATGATA[C/T]CTACGTTCTACACTG | 9886 |
rs148015761 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888930 | CATGGAAGGACACTC[C/T]GGAATTTTGATGACC | 9886 |
rs148053989 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965741 | TCTATCCGTAGTTGG[A/G]GAATAAAGTCATAAG | 9886 |
rs148124919 | in-del | -/AAAACAAAAC | 0.0667028 | 0.170006 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994919 | AGATAGATAAGTAAA[-/AAAACAAAAC]AAAACAAAACAAAAC | 9886 |
rs148161407 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876638 | AGTAATTGCCCATGG[A/G]AGCCTCCCAGAGTGA | 9886 |
rs148172627 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872220 | TCCTTACGGAACTTG[C/G]AGCATACACTGTTGT | 9886 |
rs148177996 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939003 | TTCTCCACAGAGAGA[C/T]GGAACCTGAGATCAT | 9886 |
rs148199313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892729 | GAGTGTTGAAGAGCA[C/G]AACACCAGGCTACAG | 9886 |
rs148246796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992318 | TTTATGATATAAGAT[C/G]TGTGCTAAGATATGA | 9886 |
rs148251513 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887873 | TCCACTCTTGAGGAG[C/G]AGTGTGGTACCATGG | 9886 |
rs148267737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920816 | TGTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 9886 |
rs148319166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925421 | CCAAAACCTATGGAA[C/T]ACTGCACAAATGGTA | 9886 |
rs148335255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975533 | AAAATGCTACTTATT[C/T]GCTTGCATGGAAATA | 9886 |
rs148419691 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973155 | CAAATATAAAGGTAA[A/G]CAATTATTAAGAAAA | 9886 |
rs148452567 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904772 | AGAGCTAACAGTTTT[-/A]ACCTAACCTCTTAGG | 9886 |
rs148490200 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942115 | AAAAACAAACAAAAC[A/G]AAACAAAACCCTAAA | 9886 |
rs148498705 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899523 | GACCAAACTGGGTAA[A/T]CCAGCACGATCATTT | 9886 |
rs148508448 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957246 | GAGTCCCTTGTTATC[C/T]TTATCAAATACTATG | 9886 |
rs148542953 | snp | A/G | 0.000115343 | 0.0075933 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911510 | TTTGATAGTTTCAAC[A/G]TTGGGTCTTTCGTAG | 9886 |
rs148547603 | snp | G/T | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60868995 | GCTTGGGTAAACATT[G/T]TATTACCTAGAAGTC | 9886 |
rs148578192 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921761 | ACTGATCATTAAGCC[C/T]TGTGGCCTTGAAAGC | 9886 |
rs148629420 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927714 | ATACAAAAATTAAAT[C/G]AAAATAGATTAAATA | 9886 |
rs148635880 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882572 | TTTTCTGGATATGCA[C/T]ATTAATTCTATTAAT | 9886 |
rs148646280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980505 | TGAGATGCTCTTCTC[A/G]GGTACCTTTCAGTCC | 9886 |
rs148672891 | in-del | -/AGAG | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924513 | TATTATTAGAGCTAA[-/AGAG]AGAGAGAGAGAGACC | 9886 |
rs148687649 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878160 | TGTGACTTGATATTG[A/G]TGAGTGTTGGACACC | 9886 |
rs148697925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986901 | TAACAAAGACACAAG[C/T]AGCTTCCTTACTAAG | 9886 |
rs148716566 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997920 | TGAGTGAAAAGAATG[C/T]TGTTTATAAGTCAGA | 9886 |
rs148718964 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913212 | GGTATGGAACTGTCG[A/G]CTGTAACGCCATCAC | 9886 |
rs148759042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903070 | TCCTATGGGAACATA[C/T]GGAGAGACACCTCAC | 9886 |
rs148771404 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918412 | CCCAGGAAGTTCTGC[A/G]CATGCCCACTCCCTC | 9886 |
rs148777946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889866 | AGTATTTTGTCGACA[G/T]TAAGTGCCTGATAAA | 9886 |
rs148788362 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968444 | AGTGTTTTGATTCTT[A/C]AAAATAGCAGGATAT | 9886 |
rs148822098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960333 | ATTGATTATGCTGGC[A/G]AATTTAATCAAATAG | 9886 |
rs148868024 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904846 | TCATGCCTTTCTACT[C/T]TTTTCTATAACCTGA | 9886 |
rs148886895 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891712 | CCAAAAAGTTCAACA[C/T]TAAAAAAACATAAAA | 9886 |
rs148931110 | snp | G/T | 3.29739e-05 | 0.00406028 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871565 | TATCTTCCTTCTCTC[G/T]TTCCCTTTTCACACG | 9886 |
rs148944036 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931192 | GTGAGATAAAATCCA[C/T]GTGCTACACATCTCA | 9886 |
rs148962528 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948598 | TGCTGTCATTGGCTA[A/T]TTAGGAGAAATTATC | 9886 |
rs148978925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994133 | CCTGATCTTTATTAA[C/T]TCAACGAATTGACAA | 9886 |
rs149024279 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875895 | ACGTGTGAGGGTACA[A/G]CCTTGGCTCAGCATT | 9886 |
rs149030200 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999755 | ACCTGCATGCCCTCC[C/T]TGTTAGGGAATGTTT | 9886 |
rs149076089 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871222 | CAGACTAAAGTTTAT[G/T]AAGCCTCCTAACAAA | 9886 |
rs149084085 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920572 | TTATTCTAAATGCAG[C/T]GAAAAGCCACTGCAG | 9886 |
rs149100622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970584 | AAAAATAGTTCACTA[C/T]GAAACTTTAGAATCA | 9886 |
rs149165399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883979 | CACCTTTGACCCAAG[C/T]TCAGGAGAGATTTTC | 9886 |
rs149190525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954772 | AAGGAGATAAGTTGG[C/T]CAAGTAACATTTCCC | 9886 |
rs149255696 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897467 | AGCTGAGGAGCTGTG[A/G]GCCTTGGGTTTTCTT | 9886 |
rs149274567 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885642 | GAGGCACAGGAATGC[A/G]GCTTCTCAAGGTCCC | 9886 |
rs149282005 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920237 | TGAAAAGCAAGCCAG[-/C]CGGTGGTTCACAGTC | 9886 |
rs149292389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996909 | TGTACAGAATGTAAC[C/T]ATCTGGAGAACAAGG | 9886 |
rs149347017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916786 | ATAGGGTTGCAGATG[C/G]AATTAAGGTTGTTAG | 9886 |
rs149393628 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914624 | CTGATAGCAGCCCCC[-/A]AGAAGGAATCCCCCA | 9886 |
rs149397732 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906608 | GCCTGTTTCTCCAAC[C/T]GTGAAATGAGCCTAT | 9886 |
rs149399508 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921412 | AATCAGCAGAGATGC[A/G]GCCAAGTACAGATTC | 9886 |
rs149416212 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972227 | CCATTCTACTATAGA[C/T]ACAAGCACATGTATG | 9886 |
rs149418597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938757 | TTTAGAGCAAATATA[C/T]ATTCAAGTTCTTAGA | 9886 |
rs149435873 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988442 | ACCCAACTGGTAGTT[G/T]TTCAGCCCTTGCCCC | 9886 |
rs149464147 | snp | A/G/T | 0.000313743 | 0.0125211 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875011 | CACGCCACTCGTGGC[A/G/T]GCTTTGGTCAACTCC | 9886 |
rs149487925 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991936 | TATTGTCTGTCTTCC[C/T]CTTCTAGTCCATAGG | 9886 |
rs149537905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887620 | ACAGAAGTGCAGGGC[A/C]AAGGAGCATGAGGAC | 9886 |
rs149556089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878121 | TGGGCACATTTTCAG[A/G]CTATGCTGCTTATAA | 9886 |
rs149607781 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873385 | CCACTTGCCCTCAAG[C/T]TGACTGTTAAACACT | 9886 |
rs149609202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968112 | TTCTTCAGTGCCCCA[C/T]GCTTTTCTCTCCTAC | 9886 |
rs149645985 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945242 | AAAGAGATCACTGGG[A/G]AATAAAGACACAACT | 9886 |
rs149662770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879645 | CCACTGTGACTGGCC[A/G]GTTATGAACTTCTTA | 9886 |
rs149679074 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934085 | TCTTTGTGACATAAA[G/T]AAATTTTACAAAAAA | 9886 |
rs149731034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941612 | GCCCATATTTGTACC[A/G]TTGTACTCCCAGAGT | 9886 |
rs149747234 | snp | A/G | 0.11228 | 0.208646 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990185 | AGTCGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 9886 |
rs149837891 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894514 | TAGTGAAATATTCTG[C/T]GCTCAGTCTTACTTA | 9886 |
rs149854510 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914450 | GTGGGAAACCTTACT[A/C]TTTTAAGGGTGAATT | 9886 |
rs149871225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963340 | GACGATGAAAGTGAA[C/T]TTAATCAGCAAATAT | 9886 |
rs149889772 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979656 | TCATTGCCTGCCTGC[A/C]GCTTATGTTTTAGAT | 9886 |
rs149922880 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970231 | GTGGTTACAAGTCTA[A/T]TCCAATTTTGCTTAT | 9886 |
rs149927618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908266 | TGAAGCAGAGGAAAC[C/T]GAAGGCAAGGTCTAA | 9886 |
rs149960628 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947232 | CTAAAATCATTGCTT[C/G]CTGATAGAATCAGTA | 9886 |
rs149990776 | snp | A/G | 0.000148396 | 0.00861255 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888434 | ACTGGAGCAGGGTCC[A/G]AAAAGGGCCTGGCTG | 9886 |
rs150012070 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954073 | GTATGTGTGTGTGTG[C/T]TTGTGTGTAGTTTTA | 9886 |
rs150112917 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996098 | AAGTCAAAGAACTCA[G/T]AGCTCGTAAATGGAG | 9886 |
rs150115106 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910542 | GACCAAGTGCCAAAA[C/T]AACTTAAAACATTCT | 9886 |
rs150133710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923228 | TACAAGCAATTACCT[A/G]AAGGCACAGAAAACA | 9886 |
rs150173570 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891500 | TGTGCACCACCAGTC[A/C]TGGCTGATTTATTTT | 9886 |
rs150183680 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966859 | CACCCCACAACAGGC[C/T]CCAGTGTGTGATGTT | 9886 |
rs150185540 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930816 | AGGTTCTTCTTCATC[C/T]CTTCTTACAGGGCTA | 9886 |
rs150202016 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982350 | ATACCATTTAGGTGA[A/T]GTGGAGTTCCTTCTC | 9886 |
rs150224781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886388 | TCTTTGAGCTTTGAC[A/G]CACCCAGCTCCCACC | 9886 |
rs150323282 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955888 | TATTTTGTTACATTT[A/G]TAACAACTTTTAATT | 9886 |
rs150375398 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961538 | AGCCTCATAAGAATG[C/T]CACATGGATCTAGAT | 9886 |
rs150412683 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936924 | ACTTCATAGCACTGG[G/T]AAAGACATATACTTG | 9886 |
rs150437557 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957460 | TGTTCACAGTTGACT[-/G]GAAATGTCATTATAT | 9886 |
rs150453093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883694 | ACAAGAGGTAAAGAA[G/T]ACCATCACTACCAAC | 9886 |
rs150471788 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872915 | CAACTATCTACTCCC[A/C]CATTCCCTCCCCAGA | 9886 |
rs150482451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991390 | GACTTAAGCAGTTCA[C/T]TCCTCTTCTGCACTC | 9886 |
rs150499467 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933957 | GAGATTGAGATATAG[A/C]TATACTAAAATATTA | 9886 |
rs150516216 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984394 | TGTTTTATGCATATG[A/T]CTATTCTGAATGTTC | 9886 |
rs150520523 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888983 | GGAAGGGTGCCTGAA[A/G]TAAAGGTTTCTGGAC | 9886 |
rs150589019 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916689 | TGCATTGCATATGTG[A/G]TATGCAGAATAATAG | 9886 |
rs150613952 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881284 | CTGGTATGTCTTCAT[C/T]AGCAGCATGAAAATG | 9886 |
rs150638003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957430 | ATAATGTTATGGGAC[C/T]GCTGTCGTATGTGCT | 9886 |
rs150675563 | in-del | -/AA | 0.470246 | 0.118286 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882204 | AGTTTCTTTTTTCTT[-/AA]AAAAAAAAAAAGAGT | 9886 |
rs150701810 | snp | C/T | 0.0011531 | 0.0239837 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892917 | GCAAAAGTGCTTGAT[C/T]TCTGGATACCACATG | 9886 |
rs150726127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940406 | AGCCTGTTAATTCAG[A/G]CAAAACCTGAAAAAG | 9886 |
rs150753664 | snp | C/T | 3.30748e-05 | 0.00406649 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888258 | TATCCGATTGGCTTT[C/T]CTTACGTGAAAGGCT | 9886 |
rs150778363 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946730 | GCAGGTGCCTATACC[A/G]GAAAGACACACAAAG | 9886 |
rs150791101 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907476 | CCAGAAAAGAGCTTC[A/G]AAAGTTCATCCAAAA | 9886 |
rs150830693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953292 | AATAAGCTATACATA[C/T]AAGACCCCATTAGTT | 9886 |
rs150843388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903399 | CCCAGTGAGAGGACC[A/C]ACTTGATCACTCAAC | 9886 |
rs150847345 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998295 | ATAAGAGATAATTAC[G/T]TATTCAAACATACTT | 9886 |
rs150868466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925841 | CTAGACATATACAGC[C/T]TACAAAGATAGAGCC | 9886 |
rs150950312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879185 | ACCCAGGGAGTATGA[C/T]GCGAAAGTGTATGTT | 9886 |
rs150951862 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960684 | ATCATAATCCAAGTC[A/G]TAAAGAACTTGAAAT | 9886 |
rs150970490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973596 | ACAACACCAACAACT[A/G]AGATAATGCCATCAG | 9886 |
rs151001921 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875162 | GGACACAGCTCTGGG[A/C]AGGCATCTGAATTAA | 9886 |
rs151022148 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982057 | ATTACAGGCATGAGC[C/T]ACTGTGGCTGGCCTG | 9886 |
rs151093995 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948821 | CTTTCTGGCTTCCTA[A/G]AGAGGAAGAGGCTGG | 9886 |
rs151112921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963145 | ACCATTTGGTTTGAC[C/T]AAAAGTTATGGCAGG | 9886 |
rs151144512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883010 | GTTATCCCCATTTTA[C/T]AGATGAGGAAACAGG | 9886 |
rs151162531 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999771 | TGTTAGGGAATGTTT[A/C]TGGTTCAGACACACA | 9886 |
rs151181786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900463 | CTGCTTCCCTGTTCC[A/G]GGAACTGACACCTCT | 9886 |
rs151183525 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966671 | ACTTCTTTTTTTTTT[G/T]GTTCTTTTTTTTTAA | 9886 |
rs151183554 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927799 | ACTCTAGGACATTGG[A/G]CTGGACAAAGATTTC | 9886 |
rs151235312 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936563 | TAAAATAAGGCGGTC[C/T]GGTTATGGCCTATTA | 9886 |
rs151251473 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986967 | AAATTGTTGATTGCC[A/G]GTGGCTCCAGGCCAG | 9886 |
rs151278163 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888339 | CATCATCCTCAAATC[A/G]AACATCTCGAGGACC | 9886 |
rs151302799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991187 | AACCCATATTCCACA[C/T]GGTAGCCAGAAATAT | 9886 |
rs151323636 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918782 | ATGGAGTTTCACTCT[C/T]GTTGCCAGGCTGGAG | 9886 |
rs180792906 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899461 | TTCAGTGTCAGCTAC[A/C/T]GCGCTACATGGGAGG | 9886 |
rs180807180 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880537 | CATGGTTGGTGAAAA[C/T]GACAATTATGATTCC | 9886 |
rs180863969 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983841 | TTCCCGGCCCCGCCC[C/T]CCTTCTGGCCTGTCC | 9886 |
rs180901392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970494 | ATTGAATATTAATTC[C/T]GTATTTCATAGATCT | 9886 |
rs180902399 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003456 | GGGATTACAGGGTCA[A/T]ATGGTCTTTCTAGTT | 9886 |
rs180915738 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925555 | AAACTAAACCCAAAA[G/T]TAGTAGAAGAATTAA | 9886 |
rs180924781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905848 | CTGATCCTTACTTTT[C/T]TGCTTGCCGTAAAAC | 9886 |
rs180938743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872051 | ATCTCACATTAATAT[A/G]TGACCACCAGCCAGT | 9886 |
rs180940391 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952088 | CAAAAAAGAACGGTA[A/C]ATGATAAAACTTTTA | 9886 |
rs180944567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974874 | TTTTCTGTGGGGTAG[A/C]GAAGGCATCGTGATG | 9886 |
rs180947238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891890 | AAAGGTAACTGAATC[A/G]TGGGGGCGGTTCCCC | 9886 |
rs180951852 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933586 | TTAGCTGGGTGTGGT[A/G]GCACGTGCCTGTAGT | 9886 |
rs180955261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920342 | GGATGTCGAGAAAAA[A/G]TAATGGATGGGAAGC | 9886 |
rs180957305 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941994 | CTTTTGCTAAGTGCC[A/G]GTGTTAATGTGGCAT | 9886 |
rs180964913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961287 | CACAGTATGCCTAGA[C/G]CTGGACACATCTGGA | 9886 |
rs180977138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912039 | AAAAGCAGTTTTCTA[C/T]AGGTTCAAAACTGTT | 9886 |
rs181080625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908774 | GTTTTTATTCTTTAA[C/T]TAGAGGTGGGGTCTG | 9886 |
rs181110219 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956712 | ACACATTAGCCTAGG[C/G]TTACACAGGGTCAGG | 9886 |
rs181111629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875970 | CTTCTAATCCAGCAC[A/G]TTGTCCAAATCATGC | 9886 |
rs181112019 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937703 | ACTGGGCCACTGGAA[C/T]CCAGAGAGACCACTC | 9886 |
rs181118576 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894179 | CAACCATAAAATTTC[C/T]AAAAATAATCACTTG | 9886 |
rs181121946 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916807 | AGGTTGTTAGTCAGC[C/T]GACCTTAATATAAGC | 9886 |
rs181123019 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923123 | GAATATACTTCAATC[C/T]TTGGCCTTTGTGAAT | 9886 |
rs181124508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903054 | GGGATTTGCAAAGCT[G/T]TCCTATGGGAACATA | 9886 |
rs181218006 | snp | C/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987846 | AATGCTCTCCACCCC[C/G/T]TAACCCCTGACAAAA | 9886 |
rs181239924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948681 | AGGGGTTTGAAGCAC[A/G]AAAGAGAATAAGCTC | 9886 |
rs181255525 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972168 | CAGAAATACCATTTG[A/C]CCCAGCAATCCCATT | 9886 |
rs181262419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966191 | AAAACTTTTAATATT[A/C]GTTTTCTCTGATGTT | 9886 |
rs181268651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978503 | AAGGCTAAGTTGGGA[A/G]AGAGAGTGGGTATGT | 9886 |
rs181274766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926448 | AAAGCTATAGGCCAA[C/T]ATATCTAATACACAT | 9886 |
rs181283905 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913441 | TCCAATTCTGATGAT[C/T]GGCCAGGCATGGTGA | 9886 |
rs181303638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975469 | ATAGGCATGTTTACT[C/T]ATAAGAGTTTTTAAG | 9886 |
rs181305156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962230 | TTTATATGCAGCTAG[C/T]AGTCTGTAATTCTTT | 9886 |
rs181305518 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931224 | TCTTTTAAAGTATAC[A/T]ATTCAGTGGTGTTTA | 9886 |
rs181315700 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943645 | GCGCCTTCTCGTCGG[A/C]GCGGCACCACCCCCT | 9886 |
rs181332853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999604 | ATGATATTGGAGGAA[A/T]CAATAATTAATCCAA | 9886 |
rs181365013 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969423 | TGTAAAACATTAAAA[A/C/G]TCAGAGTATGTTCAG | 9886 |
rs181388653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933326 | TCTGGAGTGCGACTA[A/G]AAATTTTAAGGCAAA | 9886 |
rs181395184 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891059 | TTGCTGAGGCCAGGA[C/G]AGTCTCTCATTTACT | 9886 |
rs181399210 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003369 | ATTGTGAATAGTGCC[A/G]CAATAAACATACATG | 9886 |
rs181429791 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994631 | AGATATCCTCAGGAA[A/G]AAAAATGCAATGCAT | 9886 |
rs181436165 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871279 | TGCAGTGAGAGTCAG[C/G]TTCCCTTTTTGTCCA | 9886 |
rs181439860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881315 | GACTAATACAATTAG[C/T]ATAGTTTTTTAAATA | 9886 |
rs181455269 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905700 | TCCACCTCCTGGTCC[A/T]CTTGAAGTTTCACTG | 9886 |
rs181508847 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952041 | CCAGCCTGGACAACA[C/G]AGCGAGACTCTGTCA | 9886 |
rs181527388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900053 | CTGCCTGTGGTGCCC[G/T]CCTGGAGGAAGGGAC | 9886 |
rs181556264 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983238 | TAAATGAGAAGAAAT[G/T]CTTCCTTAGGGCTAT | 9886 |
rs181565901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978149 | CCCTCTGCATTAAAT[A/G]TATATTTTTGCCTAT | 9886 |
rs181566007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999172 | ACTTGGATAAAGGAG[G/T]AGTGGCGGCAGAGGG | 9886 |
rs181583565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931153 | AAATTTTCTACAATG[C/T]ACGTCTTATTTTTTT | 9886 |
rs181584050 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919773 | TGATTCTCACCAGGG[A/C]TCTCTGACAGTGGAG | 9886 |
rs181586163 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916062 | GATGAAATAAGGCCA[C/T]GGCAGCAACTCCCAT | 9886 |
rs181607132 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965715 | TTTTTCCATTACCTT[A/C]ATTCTCATGGTCTAT | 9886 |
rs181608663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948073 | ATGAATAATAATGTT[C/G]AATATATTTTCATTG | 9886 |
rs181718350 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899921 | GTGGCTAGGGAGGGC[C/T]TCGCTGAGAAGGTGA | 9886 |
rs181732622 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958514 | TGGATTTCCAAAACA[C/G/T]TTTTTTTCAGGAGAA | 9886 |
rs181745863 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925849 | ATACAGCCTACAAAG[A/T]TAGAGCCATGAAGAA | 9886 |
rs181755177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912883 | TTGTTAAACTAATAA[A/G]AACAGATGCTACACT | 9886 |
rs181755675 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989133 | ATATTTTTTAATAAT[A/T]AGTGACAACAGCAAG | 9886 |
rs181756842 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885306 | TATAATAATTATTAT[C/T]TGTCAGTTAAAAGTA | 9886 |
rs181757092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880888 | ATTTACAGGTATCCA[C/T]ACAAATTTGTTTCTG | 9886 |
rs181791610 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902988 | TAGGATAAGGGGAAT[A/G]GGAGAAAATTAAGGA | 9886 |
rs181808173 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923834 | CATTTTTTTCCTTGT[C/T]TGCCTCTCACCTTCC | 9886 |
rs181907175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984730 | TTTAAAATCTTTCGA[C/T]AATTTGTTCATGAGC | 9886 |
rs181918043 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972677 | TATCCCAGAACTTAA[A/G]GTATAATAAAAAAAG | 9886 |
rs181936279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890245 | AATCCCTTCTTCAAG[C/G]CTTCTTTTGCTTGGA | 9886 |
rs182023925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930584 | ACTGTCTTAGCAGAG[C/T]GACATAGCAGAAAGA | 9886 |
rs182030769 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988088 | AGGCGCCCACCACCA[C/T]GCCCGGCTAATTTTT | 9886 |
rs182031141 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915891 | ATTTCTTCTCTCCTT[C/T]AGTGCCAGTGATCTT | 9886 |
rs182035959 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884196 | CCAAGGCTTGTGATT[C/G]TAGGATTCTATTTCC | 9886 |
rs182036721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972463 | CATCGCATGTTCTCA[C/T]TCATAAGTAGGAGAT | 9886 |
rs182036987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957977 | ATTACTGAAAAGTGG[A/G]ATGACTTACTGTGAG | 9886 |
rs182039066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901704 | CTTTTCTTCTTTCAT[C/T]ATGAAAAGTCAACAT | 9886 |
rs182058678 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938919 | AGTAGGGGCATAAAT[A/G]CTAGTTTATTGTTAT | 9886 |
rs182059860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975265 | GTAAATGGCTGGTGT[C/T]TTTAGGCCATGACAA | 9886 |
rs182072394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942545 | CCAAATATGATTCAG[C/G]AATCTCAGAGGAAAC | 9886 |
rs182115339 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990346 | TCTAGTGGACACCAA[C/T]AGGCCAATGATTTTT | 9886 |
rs182151115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966927 | TATATAGCAGCACTG[C/T]GCCAGGCACTGGGGA | 9886 |
rs182211426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921699 | CCTTTCTTAGAAAAC[C/T]TTCCACCTGGGGCTG | 9886 |
rs182216142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906868 | AAAAGGGACTGATAT[A/G]GTTTGGCTGTGTCCC | 9886 |
rs182221454 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938314 | AGATTTAGAAGACTT[G/T]GCACTTTTCAGGCAG | 9886 |
rs182224237 | snp | C/T | 3.39847e-05 | 0.00412204 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892814 | CCTTGGCTTACCTTG[C/T]TAACGGGCGCCTGGC | 9886 |
rs182233307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971508 | TGCAGAAAACTGAAA[C/T]TGGACCCATTCCTTA | 9886 |
rs182235259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955012 | CTACCCATACTTATT[C/T]GACAAGGGGAATCTT | 9886 |
rs182239574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909203 | ATAAATGCTATGCAG[G/T]AATCTCACAAGATAA | 9886 |
rs182240950 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996327 | CAGTATTCTGAACTA[A/C]ATACCCTCAAGGCCT | 9886 |
rs182240973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935023 | TGTTTTGTTTTGCAT[A/G]CTGCTATCTGTACAA | 9886 |
rs182256206 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870909 | TTGTAATTACACCGA[A/T]GTTATTCAACAGAAC | 9886 |
rs182293631 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876243 | ATGTTCTAAACACTC[A/T]ACACTAGACAGTACA | 9886 |
rs182338503 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986465 | TATACTGGTCAACAC[A/C]GTTGAAGTGATTGAA | 9886 |
rs182361396 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961906 | CTCCGCTCCTGGGTT[A/C]AAATGATTCTCCTGC | 9886 |
rs182391441 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994061 | TCTGAAAGGTAAATG[C/T]GACTCAAAATATTAG | 9886 |
rs182430833 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999940 | AAATTTTATTTCAAA[G/T]TTTCATAGGATGTGA | 9886 |
rs182456274 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989872 | TTACCCTGGCTGTAG[A/G]AGCACCACTGATGGG | 9886 |
rs182461819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973445 | GCCTTCTTAACAGCC[C/T]TCTTTTTTGTTGTTG | 9886 |
rs182487364 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924140 | ATGTTTACATATCAA[G/T]GACAAACAAATTGTA | 9886 |
rs182494527 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910375 | TGGAAATATGTCTTG[C/T]GAAGGACTTTGGAGA | 9886 |
rs182499366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923452 | GCTGGCAACAGTACA[C/T]AGTAGACTTGAAAAT | 9886 |
rs182508103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895733 | AAGTATCACAATGCT[C/T]AAATGTCTTGTGGTT | 9886 |
rs182511161 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958908 | ACCTGGCCCAGAGTA[A/G]GATATTTAAATAAAA | 9886 |
rs182513246 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973122 | TCTCTAGATTTAAGG[A/T]TTCAATATGGACTGC | 9886 |
rs182527266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939164 | TTCGTTCTTTAGTGG[A/G]TAAAGCCTGATCAGA | 9886 |
rs182568533 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894622 | TTATTCATAATCATA[C/T]TTATATCAGGTATCT | 9886 |
rs182576209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962799 | TCGTAACAATTTTGT[C/T]TTCTTTCTGAGTCAG | 9886 |
rs182599106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927146 | TAAAACAAAATGCCT[A/C]GGAATAAACTTAACC | 9886 |
rs182630975 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900186 | TGAGAATGGACTAAA[C/T]TGGTGGCAAGGTAAG | 9886 |
rs182637242 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874155 | CAGAAAGAGGGAGCA[A/C/G]AGGAAGCCAAACCCA | 9886 |
rs182649940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873389 | TTGCCCTCAAGCTGA[C/T]TGTTAAACACTTACC | 9886 |
rs182658773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906386 | AGCTCGTAATAGATG[A/G]TGAGTGCTGGTCTTC | 9886 |
rs182659938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892524 | ACATTTTGTCTAATA[C/T]TTTATACTTTTCAAA | 9886 |
rs182670545 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959582 | AATGAAACAAACAAA[C/T]AAACAAATAGCTGAA | 9886 |
rs182684076 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979113 | GCTCTAATATTTATG[C/T]TAGGAACATGTATGC | 9886 |
rs182869581 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945572 | CCCTCCAGCCAAGAT[G/T]CCCAGGTGACTTCCA | 9886 |
rs182882675 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981258 | ACTCCAAGGCAATGC[A/G]AGGTCCCCAGAATTA | 9886 |
rs182889815 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975553 | GCATGGAAATACTAG[A/G]TAATAACTGACTAAG | 9886 |
rs182898447 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882496 | AAGATACAATGTTTT[C/G]CTGAATATTAAATGA | 9886 |
rs182905727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950750 | GGGCTCATTATGAGG[C/T]CCCTTAAACAATGCT | 9886 |
rs182929277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976898 | GTTTTAAATCATCTG[C/T]GCCTTTGACAGCTCA | 9886 |
rs182930891 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996855 | TTGATTTGCAAACTT[A/T]TCCTGAATGTTTTGT | 9886 |
rs182932422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913958 | AACTGACACACTGAT[A/G]GTTTCAAAAATTATA | 9886 |
rs182942878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964100 | AATACATGCAAACAT[A/G]AAATATAATCTTAGC | 9886 |
rs182961153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877730 | GGTGCTTAAGAAATA[C/T]ATGTTGAATTGAATT | 9886 |
rs182964794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909775 | TCCTTGTTACCAAGG[A/G]GACATTAAAATCGTG | 9886 |
rs182970200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894841 | TTAAGACACATGGCT[C/T]TAAGGGGAATCATTC | 9886 |
rs182985836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918190 | GCCTTTCTTGACTAC[C/T]CCTCTGGTCCAAAGG | 9886 |
rs183044260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950245 | ATGTATAATGTGTAT[C/T]TTTGACATTTTAAAA | 9886 |
rs183044614 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931561 | GACATATTACTTCTA[A/C/T]AATGAGAAAGACGTT | 9886 |
rs183060360 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979978 | GAATATAGTAGAATG[A/G]GAGAGGGAGGAACCG | 9886 |
rs183064054 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001026 | CTCTAATCCCTCTGG[C/G]CACCCCCGCCTCCGC | 9886 |
rs183067071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967621 | GTTTGGAAGGGAAAC[A/G]ATAGACTACTATTGC | 9886 |
rs183083408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878425 | TGACAGGTGTTGGGC[A/G]GAGCTGCAAACCACA | 9886 |
rs183127453 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934655 | AGTTCCTTTACTTGA[A/T]GCCTCTTTCCAGGAG | 9886 |
rs183187707 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968281 | GAAGGGTGGTAAGTG[C/G]GCGTGGCATGTGGTC | 9886 |
rs183209812 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001861 | GGAGGCCTCCCCAGG[A/G]CCCACCCACCTCTGG | 9886 |
rs183255103 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932368 | GGAGTGGGGTGGTGA[A/C]CAGAAGTAGGGCACT | 9886 |
rs183293852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971275 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 9886 |
rs183329968 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914154 | AGAAACAAGATGTGG[A/T]GTAGCTGATCTTAAG | 9886 |
rs183352417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60882885 | TAACAAGAAAACTCT[A/G]GCATAATAGTCGCTA | 9886 |
rs183357661 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945761 | TTCCCACGGCAGTAT[C/T]TTTGAAAATGGAGTT | 9886 |
rs183359428 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900433 | ATGATAAGCTTTTTC[A/G]TGAGCTATTTATTTC | 9886 |
rs183361977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928134 | AGATATAATCTCACC[A/G]CAGTTAAAATGGCTT | 9886 |
rs183364823 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953550 | TAACAGAGGTGATAT[A/G]CCATGTACTGTGAAG | 9886 |
rs183366884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970693 | ACTTTTTAACAGTTC[C/T]GTGGTCAGAAAAGAG | 9886 |
rs183403262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921376 | CTCCAGGAGAGAAAG[A/G]ATGGTGCCTCTGACA | 9886 |
rs183469900 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982366 | GTGGAGTTCCTTCTC[A/G]AATGACAACAGTAAC | 9886 |
rs183491412 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870191 | AGAAGCAATGACTGA[C/T]TGCCTCACGAAAGCT | 9886 |
rs183499307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932485 | GCATACATTTCTCTA[C/T]GTGTTATACTTCAAT | 9886 |
rs183500106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903487 | TGCCAGAGATTACCA[C/T]CATGTTCACCAGTTC | 9886 |
rs183511969 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905316 | TTAGCTGGGTGTGGT[C/G]GTGGGCACCTGTAAT | 9886 |
rs183518861 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886884 | TGTGTATAGACTTTT[C/T]TTTTTTTACAGATAG | 9886 |
rs183520168 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949289 | CCAGCTTTCATGTCA[C/T]GGATATGTCAACATC | 9886 |
rs183520996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904468 | CAGTGATCTACTTTC[C/T]GTCACTATAGATTAG | 9886 |
rs183521673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931449 | ATGTGGCCTATTGTG[C/T]CTGTCTTCTTTCACT | 9886 |
rs183523873 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968563 | GACCATCTTTGAGGA[A/G]CTGCAGAAAGCAGGA | 9886 |
rs183528242 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951683 | ATTTGGTGAGAGGCA[C/T]GGAAGCTTCATGCTT | 9886 |
rs183529292 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917028 | GATTCTCCCCTAAGG[C/T]CCCCAAAGTAACACA | 9886 |
rs183535388 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985789 | TTCCATTTCTTTGTT[A/C/G]AATATTGTAAGAAAG | 9886 |
rs183545951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954541 | TAGAGGACACCCCAT[C/T]ACATTCAAATATCCC | 9886 |
rs183546999 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869588 | GATATTATTGCTTAT[A/T]CCCCAAGTTCATTTA | 9886 |
rs183651768 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892202 | TTATATATAGTGAAA[C/T]AAATTCTCCTTCAAG | 9886 |
rs183652316 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883664 | ATTGGTGGCTACCCT[A/G]GCTTTTTTCTGGATA | 9886 |
rs183700179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917456 | AGAAATTCATTTCTC[A/T]CAGTTCTGGAGGCTG | 9886 |
rs183737288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887290 | CATAAGCTTTAAAAT[C/G]AATGAACTGAGTCTT | 9886 |
rs183795396 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976314 | CTTTTGACTATATGT[A/G]TATATATTATATATA | 9886 |
rs183834315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920687 | TCAAAGCTTGCTCTG[C/T]CACCCAGGCTAGAGT | 9886 |
rs183864300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873137 | ACTCACTGAAAATCA[C/T]AACCCAAACATCAGA | 9886 |
rs183883323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906285 | GAAAGCAAAAGGACT[C/T]ATGCTCCGCTACTTA | 9886 |
rs183933237 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957076 | GGGCAATAACATATA[G/T]GGAGCTGTCCTCTCC | 9886 |
rs183938915 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937747 | CAAGAAAAAAAGGTT[A/C]CTATAACCATTCCTT | 9886 |
rs183953010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996525 | TAGATGACCTGATGT[C/T]CCCCACTGTAGATGA | 9886 |
rs183953943 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987965 | TTAAGACCGAGTCTC[G/T]CTCTGTCCCCCAGGA | 9886 |
rs183970273 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972212 | CCAAATGATTATAAA[C/T]CATTCTACTATAGAC | 9886 |
rs183974059 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870323 | TTCCTTTCCGTGTAG[A/G]AGAACGCAGGCGCCC | 9886 |
rs183981765 | snp | C/G | 3.33483e-05 | 0.00408327 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888668 | TAGGCGGGCCCTCCT[C/G]CCTTTCTTCCTCTGG | 9886 |
rs184016643 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934262 | GGGAACAGGCTTGCT[A/G]CTCCTGAAACCTTCT | 9886 |
rs184030509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963278 | ATTTTGATGTCATCA[A/G]TCTTTTTCTTTGCAT | 9886 |
rs184034965 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910698 | CTTCCTCATTGGCAG[A/G]GCACGCTTCTTTTCT | 9886 |
rs184046619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879069 | TAGAGAGAAGGGACT[C/T]ACTTTTGCCATTTTA | 9886 |
rs184080308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941700 | AGTCAAAGACAAAAT[G/T]TTTAAAAGACAAATG | 9886 |
rs184082018 | snp | C/G/T | 0.00637415 | 0.0561569 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925259 | CAATTAAATCTCTTT[C/G/T]CTTTATAAATTATTC | 9886 |
rs184091465 | snp | A/G | 2.14728e-05 | 0.00327658 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911307 | AGACTGGCAACCAGC[A/G]ATGATGTGCCCTAGG | 9886 |
rs184100281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975062 | TTCCTTATAGCAGCA[C/T]GCCAATATACTAATT | 9886 |
rs184103667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993110 | AATGATGGAGGGGAC[A/G]TGTCTCTCTGCTTGG | 9886 |
rs184111974 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974331 | TGACTAAATCAAGAG[A/C]TATAAATAGACATGA | 9886 |
rs184112171 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961232 | GTCCTTGTGAACATA[C/T]AGGAAACCTTGTATT | 9886 |
rs184131611 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002757 | CTTGGAGTTTATGCA[A/T]ATGGTTATGCTAGAA | 9886 |
rs184159534 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897279 | CTCAACTTTTTTTCC[A/G]ATCTGAAATACCAGA | 9886 |
rs184176671 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924771 | AGTCTCAAAAATTTT[A/T]AAAAAATTATATCCA | 9886 |
rs184192016 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942435 | CAATCATGGGCAAAA[C/T]TAGTATATTGACTAT | 9886 |
rs184206170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912193 | AATTCATAAATATAT[A/G]TGTGTGTGTGTATAT | 9886 |
rs184254712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993854 | AATATGAGCATTAAA[A/G]TTTATAATTCTTTTG | 9886 |
rs184262290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961332 | CCACTGCTTACTAGC[A/G]GTACAATTCTGGATG | 9886 |
rs184343681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925695 | AAAAAAAAGAAGACC[C/T]GAATAAATAAAATCA | 9886 |
rs184349850 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901052 | CCAGGTAAGTTACAA[C/T]AGAATTAAGGCTTAA | 9886 |
rs184354950 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899570 | GGACTCTACCCAGCC[G/T]CCTTGGCAACTCTCT | 9886 |
rs184382346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930179 | CCACATCTTTAAGAA[A/G]AAAAATGAAAACAAC | 9886 |
rs184389810 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945945 | AGCGCTTTGGGAGGC[C/T]GAGGCGCGCGGATCA | 9886 |
rs184395655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908370 | AATACATTTTCAAGA[A/T]TAGGGAATGTATTTC | 9886 |
rs184403720 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929143 | CCCACCAGGCCCCTC[C/T]TTCAACATGTGGGGA | 9886 |
rs184418288 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875853 | ATCTCTTGCCTTTGT[A/G]AGGGCTGTCACCTGC | 9886 |
rs184424519 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893903 | TCATTCTAGGTTAAA[A/T]TGTGCTGAATGATGA | 9886 |
rs184436077 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922747 | ACCATCCCTTGCTGA[A/G]GATGGACCAGGTAGA | 9886 |
rs184468981 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968996 | ATATTTTTTAAAAAT[A/C]AGGTATTTGAATAAA | 9886 |
rs184492331 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003077 | AAAGCTATCCCTCCC[A/G]CAGCCCACCACCACC | 9886 |
rs184503765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982987 | TTCCATGGTCTTTTA[A/G]TCGACAGATTAATTC | 9886 |
rs184515686 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964497 | ACCCTTAAAAACTTT[A/T]CATTGCATGCTTTTC | 9886 |
rs184516595 | snp | A/C/G | 0.0127048 | 0.0787486 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915467 | AAAGAAAAGCCTGAA[A/C/G]GAATGGACACTGGTA | 9886 |
rs184538034 | snp | C/T | 0.000134447 | 0.00819789 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911020 | GAGAGCATCTGTGCT[C/T]GGTGTCAGTCAGAAG | 9886 |
rs184543019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997636 | CTGTAAATTTTCTAT[C/T]TGGACTGTCCAAGCA | 9886 |
rs184566035 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940955 | CTTCCATAAAATCTT[C/T]AAGGCCAGAGACCCC | 9886 |
rs184568378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898316 | GTAGGTTCTTTACAG[A/G]AACATTTTCAAAACC | 9886 |
rs184577132 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924959 | TAGAGTTGGGGCTTG[A/G]TGGCAAGTGTTTAGA | 9886 |
rs184617118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930834 | TCTTACAGGGCTAGC[C/T]ATCATTCTCTGCTTG | 9886 |
rs184617544 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971585 | AAGACCTAAAACCAT[A/T]CAAACCCTAGAAGAA | 9886 |
rs184621593 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915944 | CCATCCTTTTGGACA[C/T]GTGCTGGATATTGTT | 9886 |
rs184630566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902005 | GAGCCCCAGGCATCA[A/G]TCAAGCCCTGTTGCT | 9886 |
rs184633858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977380 | CTTATGTATGGCTGC[C/T]TATGCTCCTCCATAC | 9886 |
rs184642345 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964984 | ATACTAAAACAAAGT[C/T]TCTGGAAATAAACCC | 9886 |
rs184653457 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946424 | TCACGGCCCTCATAT[A/G]TGGGGGGGCACAGGG | 9886 |
rs184657503 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986983 | GTGGCTCCAGGCCAG[A/T]TGCTGCTCATTAATG | 9886 |
rs184657528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947227 | GTATACTAAAATCAT[A/T]GCTTGCTGATAGAAT | 9886 |
rs184678832 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884259 | CACAATGGGAGTGCT[C/T]GAATTTCTTGTGCTA | 9886 |
rs184717712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898921 | ATGCCACCAAACCCT[A/G]AGGTAGATAATATTG | 9886 |
rs184772353 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945976 | CGAGGTCAGGAGTTC[C/G]AAACCAGCCTGGCCA | 9886 |
rs184801745 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870722 | AGTTTGCCCTGGATA[A/G]TGCTGGGATTTAATA | 9886 |
rs184808556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890021 | CACAATAGCCCTGTG[A/T]GGTATTATTTCTGTT | 9886 |
rs184846025 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880412 | GCAGCCACCAGACAC[C/T]TCAGAGAGGGAATAT | 9886 |
rs184846645 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983352 | ACTGAATGAAATTTG[C/T]TTATTATAAGACATA | 9886 |
rs184883340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904987 | TTGGATTACTTTTCC[A/G]TAAAAAGCACATGCA | 9886 |
rs184885187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883350 | TGTGCATTCACATTC[A/G]CTGCCAAGTTTTTGT | 9886 |
rs184937182 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003410 | TTTATAGTAGCATGA[C/T]TTATAATCCTTTGGG | 9886 |
rs184988324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971881 | AAAAACTGGGAAAAG[C/G]ATATGAACAGACACT | 9886 |
rs185015176 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900850 | CTGGTATACGGCAGA[C/G]GTTAACCGGTTAATC | 9886 |
rs185063102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937584 | GCCACAAATCTGCAA[A/G]AGAAGCTTGGTATTC | 9886 |
rs185103144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987773 | TCTGAGATCAATATG[C/T]TTTACCACTTTCCAC | 9886 |
rs185118627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952284 | TTGAGATCATAAAAA[A/T]ATGTTTCACAAAGAT | 9886 |
rs185122770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933828 | AAAATGTGTTATAGG[A/T]GTACACTCATTGTTA | 9886 |
rs185135402 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920409 | TCATTCCTGCCATCT[A/G]GAGAATGAGAAGGGC | 9886 |
rs185141787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984147 | ATCAACCAGTTAATA[C/T]GCACGTACCTTGAAA | 9886 |
rs185157728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956308 | CATTTACTAGGAATG[A/G]AACATGCAGGACTGG | 9886 |
rs185163442 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970521 | ATCTTGGTAATTGTA[C/T]TAAGTTCAATGCTTC | 9886 |
rs185175048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892011 | CTCCTGCCGCCATAC[A/G]AAGAAGGATGTGTTT | 9886 |
rs185195596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905999 | ACTTCAACATGAAAC[C/T]AGACATACAGAAACC | 9886 |
rs185200653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960700 | TAAAGAACTTGAAAT[G/T]ATTACAATTAGATTG | 9886 |
rs185208744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905406 | AGCAAGCCAAGATCG[C/T]GCCACTGCACACCAG | 9886 |
rs185217673 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871230 | AGTTTATTAAGCCTC[C/T]TAACAAAAAAAATAT | 9886 |
rs185288055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890310 | CACCCACTCCTCACA[C/T]TTTAGTCCACAGTCC | 9886 |
rs185312923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919434 | AATCAGCAGTTGTAG[A/G]TAGGTGGGAGCTGTT | 9886 |
rs185323896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991591 | GCATGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 9886 |
rs185331083 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869142 | CAGATTATACTAAGT[A/C]CTGTAGGATAGTTCT | 9886 |
rs185337480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908881 | GGCCCTAAGGAGAAC[A/G]TGGCCAGAAACACAG | 9886 |
rs185342246 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933096 | CAACGTTAGACCATA[A/C]ATGCAAAAGTGCTGG | 9886 |
rs185446511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951879 | CTGGTCAACATGATG[A/G]AACCCCGTCTCTACT | 9886 |
rs185449935 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973942 | GTAGTTTAGGCCAAA[G/T]AGTTTACCTGAAGAT | 9886 |
rs185470897 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903095 | CCTCACCTGGATTCC[A/G]AAGGTGACAGAGAGG | 9886 |
rs185476667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923264 | TCCACTTAGATAAAC[A/G]TGCTATATAAAACAG | 9886 |
rs185490531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886515 | CCTTGCTATGCAAAA[C/T]TTCAAGCATATAAAA | 9886 |
rs185493418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977916 | GAAGTTCATGTAGAC[A/G]TAAATTAATCATTTA | 9886 |
rs185511429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893634 | TTAACATATAACTAG[A/G]CGAGAATTAGATTGA | 9886 |
rs185532023 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962375 | TGATAAATACAAGTG[C/T]GCAGACATGACAGGG | 9886 |
rs185532481 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922287 | GAATAAACGAGTTCA[C/T]TCTATGCCCAAAAGA | 9886 |
rs185534117 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943793 | CCCCGGCCTCTCAGA[A/G]AGGCGAGGGAGGCCC | 9886 |
rs185565626 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975486 | TAAGAGTTTTTAAGT[A/G]ATGTGTAAACTAAAT | 9886 |
rs185571598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995246 | ACTGTGTACCAGGCA[C/T]CTTACTGAGGACTCA | 9886 |
rs185602799 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935729 | ATTAAATAAATTATA[C/G]CAAAAACAAAGATAA | 9886 |
rs185607277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919952 | TCTTGAAAAAATAAA[A/C]CAAAAATTTAAAAGA | 9886 |
rs185615609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905722 | GTTTCACTGTGCAAC[A/G]GGCTGCTTGCCATCC | 9886 |
rs185638104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891672 | GTATTAATATCAAAA[G/T]TTTTTGAAAAGGAGT | 9886 |
rs185670771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965866 | TCTTGCCTTGTTGGC[A/G]ATTTCATTGTTCGAA | 9886 |
rs185674064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907732 | ATCTCTTCTAGTTCC[A/G]ATCTTTGCACAAATC | 9886 |
rs185676296 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871401 | GTATCTCTAACAAGA[C/T]GAATTTTATAGTAGT | 9886 |
rs185677536 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924052 | AGAGGAAGGAGCAGG[C/G]AAAAGCAAGGAGGAG | 9886 |
rs185682860 | snp | C/T | 0.000198128 | 0.00995111 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874998 | CTCCGTCAATGCCCA[C/T]GCCACTCGTGGCGGC | 9886 |
rs185686232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910011 | CTCAATACCAAGGAG[C/T]AATTCACGTGCTTGG | 9886 |
rs185688212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948492 | CCTGGGGCCAATGCA[C/G]CTGGTCACAGCAGTG | 9886 |
rs185710893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978256 | AGAAGTTATTGGCCA[C/T]GTTAAAACAACTTTT | 9886 |
rs185714850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999319 | AACTTCATTAAGGTC[A/G]CAGCTTAACCTGCTA | 9886 |
rs185715171 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938937 | AGTTTATTGTTATCA[A/C]AGCAGTCATTAGGAG | 9886 |
rs185734590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878415 | CCTAGCAACATGACA[A/G]GTGTTGGGCGGAGCT | 9886 |
rs185742624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895634 | GTCTCAAACTCCCCA[A/C]CTCGGGTGATCCACC | 9886 |
rs185758560 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998105 | TGGGGTTGTACTAGG[A/T]GCAGTGTGTCCATTT | 9886 |
rs185843943 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880693 | ATAAAGTAGCTGTTG[A/T]GCATGCTAGATCATC | 9886 |
rs185918891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975744 | ATAAGCATCTCTCTT[C/T]GAAATGTTTCATTTT | 9886 |
rs185940207 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872679 | TCCGCAATGGAATAC[C/T]TCGTGTCGCATGTCA | 9886 |
rs185960064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876050 | TGGTCAATACAGTAT[C/T]GGGAATGGAATGATT | 9886 |
rs186026333 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912939 | CAATGGAAGTCCATT[A/G]TTAAACTGAGAAAAG | 9886 |
rs186038468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899923 | GGCTAGGGAGGGCCT[C/T]GCTGAGAAGGTGACA | 9886 |
rs186039756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996495 | CTGAGGAATTTGCCT[C/T]GCTGTCCACCATTGT | 9886 |
rs186054284 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999750 | CAAAAACCTGCATGC[C/G]CTCCCTGTTAGGGAA | 9886 |
rs186054881 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962106 | AGCCACTGTGCCTGG[A/C]CCATTTATAATGGCT | 9886 |
rs186056629 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942631 | TTATTTATGCTGAAA[A/C]GAGCTTGTGTTTATT | 9886 |
rs186100544 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894210 | CAATGCAGAAAACTG[A/C]AGGGTGCTTACATTA | 9886 |
rs186133723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966328 | AAAAGCAAAAGTTAC[C/T]TTAAAATAGCAAGTT | 9886 |
rs186144075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931336 | ACTAGCAGTCATTCT[A/T]TATTCTCGTTCTCCC | 9886 |
rs186201952 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984966 | TCTCCTTAAGGACTT[C/G/T]TACTTTATTATGATT | 9886 |
rs186209386 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978797 | AGAACTACTTATACA[A/G]AACCTGTAATCCACT | 9886 |
rs186234336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916855 | CTATGTGGGTGCAAC[A/G]CAATCACGATGGTCC | 9886 |
rs186260012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900082 | ACCATGCCATTCTGC[G/T]GGAGCACAGTCGTGA | 9886 |
rs186269142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948859 | TTTATACTGCTCATG[A/C]TTATGGATTTTCTGA | 9886 |
rs186278912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926514 | AAATTCAACAACACA[C/G]TAAAAAGATTATTCA | 9886 |
rs186289545 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952047 | TGGACAACAGAGCGA[G/T]ACTCTGTCACAGCCC | 9886 |
rs186445519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913497 | TCAGTTTTAAACTTC[C/T]ATGGTTTTCTTAGTT | 9886 |
rs186448554 | snp | A/G | 0.115788 | 0.21092 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933495 | GGGAGGCTGAGGCAG[A/G]CAGATCACAAGGTCA | 9886 |
rs186460102 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881619 | CTCAGTCTCTTCATC[C/T]GTTACATGGGAGGAA | 9886 |
rs186483017 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988170 | CGACCTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 9886 |
rs186485455 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921791 | CAGCAGCGTGTGGCT[A/C]AGCCTGCAGTTGGTG | 9886 |
rs186488199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931488 | TATTTTCAATTTTCA[C/T]CCATATTGTAGCACC | 9886 |
rs186496701 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917045 | CCCAAAGTAACACAG[C/T]CTGCCAACACTTCAA | 9886 |
rs186510970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979361 | TAAAATGCAAACTTA[C/T]CTAGTTAAAGTTTAT | 9886 |
rs186513703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967300 | GTTTTTTTTTTTTTT[C/T]TTTTCTTTTTTAGAC | 9886 |
rs186562562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972902 | AGGCAAAATACCCAC[C/T]GATGTTAACAAAACT | 9886 |
rs186590405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885399 | TGTCTCTTCTAGAGA[C/T]AGAGCCAGGGGCTGA | 9886 |
rs186621427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971519 | GAAACTGGACCCATT[C/G]CTTACACCTTATACA | 9886 |
rs186625200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969493 | AAATAGTGAAGTGTT[A/G]GAAAGGAGCTTGTCA | 9886 |
rs186626261 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955119 | GTGCCATCTCTGCTT[A/G]CTGCAACCTCCACTT | 9886 |
rs186627057 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882736 | TATGTTAATCATGGA[G/T]CATTAACTGAGTGCC | 9886 |
rs186627629 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935140 | GACTATTTATACAAT[A/G]GAATATTATACACTA | 9886 |
rs186634647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916240 | ATGCTGCCACAAATC[C/T]GCCATGTGAGGAAAG | 9886 |
rs186642531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986740 | AAGGGCAAAACAGTA[C/T]TTTTGCTTGGAGGTA | 9886 |
rs186748128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973143 | TATGGACTGCCTCAA[A/T]TATAAAGGTAAGCAA | 9886 |
rs186748356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959046 | CAGGACTAAGTGGTC[A/G]GGAATGCAAAGTTGC | 9886 |
rs186753833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918522 | TTTGCTCAGACAGGC[A/G]CACTTCAGTGTAGGG | 9886 |
rs186761723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905182 | CAGGCTGGGCATGGT[A/G]GCTCATGCCTGTAAT | 9886 |
rs186762120 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939394 | TTACAAACTAAAAAT[A/T]AAAAAATTATGATGC | 9886 |
rs186783420 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990044 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 9886 |
rs186798559 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870371 | TTTCACAGGCTCCCA[A/G]TGCATTTCAGCAGAA | 9886 |
rs186803426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889392 | TTCAAATATTTCAGA[C/G]TTTCAATGCACATAA | 9886 |
rs186813458 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924199 | GTCTTCCAAAACTAA[C/T]GGACACAAACCCTCT | 9886 |
rs186815735 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958745 | AGCTGGGATTACAGG[G/T]GTGCACCACCATGCC | 9886 |
rs186859121 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903017 | GAGCCAATTTTCCCG[A/C]AATACAGTTATTGCT | 9886 |
rs186883252 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994406 | TCTGGGCCAAGCACC[A/G]TCTGAGGGAAGAATA | 9886 |
rs186896420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971177 | CTTTGTATTTGTAGA[A/T]ATTATTTATAAAATT | 9886 |
rs186927044 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873570 | CAGACACAACTGCAA[A/T]TCATTCCCTCAAGTG | 9886 |
rs186935225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892527 | TTTTGTCTAATACTT[G/T]ATACTTTTCAAAGTG | 9886 |
rs186937040 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989292 | AAATCTGAGGGAAAA[C/T]GTTGCACTTGTTTTA | 9886 |
rs186961014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873167 | AGACAGTTTTAGCTG[A/G]TGCTTCCAACTTCTC | 9886 |
rs186963822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934363 | ACTTATATCAAAGGA[A/T]CTAATACCTCAATAG | 9886 |
rs186981078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906289 | GCAAAAGGACTCATG[C/T]TCCGCTACTTAATGG | 9886 |
rs187066505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934765 | GGCCAAATCTCATCC[C/T]TATTTAGAGAGAACA | 9886 |
rs187072420 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921573 | TTATAAATTTTTGGC[A/T]ACAGAAATTGTTATT | 9886 |
rs187077167 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906798 | ATGAAGGAAATTTTA[C/T]AGGGGAAAAAAAAAA | 9886 |
rs187095367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954346 | AATTATTATAAAAAT[A/G]CAGAAGATATAGCAG | 9886 |
rs187133903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923491 | ATTAATTAGTGAGGT[A/G]CAGGTCAAGCCTAAG | 9886 |
rs187140940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894767 | AGGAAATATATCCAG[A/C]ACCTAAATGTGTTAT | 9886 |
rs187157133 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975287 | CCATGACAACCTAAT[A/G]CATTTTTCTCTCACC | 9886 |
rs187161013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920895 | CTCCTGAGCTCAAGC[A/G]ATCCTCCCACCTTGG | 9886 |
rs187162754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892339 | ACACTGTCATCTTGA[A/G]AATGAAATACTGTAA | 9886 |
rs187178563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977000 | AAATTTTTTAAAATC[C/T]TAGCTTCATTGGCTA | 9886 |
rs187182981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997030 | ATGCTTGATTTGAGC[C/T]AATATCAAGTCTAGT | 9886 |
rs187195581 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964350 | GCCACCACTGCCCTC[C/T]AGGGGACACATGGAA | 9886 |
rs187276582 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957995 | GACTTACTGTGAGCA[A/G]ACACCACTTGTGAGT | 9886 |
rs187291684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938577 | TTAAAATGACCTAAG[C/T]AGTTAGCCAATTTAT | 9886 |
rs187334821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909211 | TATGCAGGAATCTCA[C/G]AAGATAATGAAGCAG | 9886 |
rs187375892 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911050 | GTTCCCCAGGAGAAG[C/T]GTGTTCAAGTCAGCA | 9886 |
rs187431259 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893072 | ATGGTTCCTCTCAAA[A/C]CCCATCCTTCTAATG | 9886 |
rs187437287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913990 | TCATGATGCTGAAGA[C/T]GAATGTCTTCAGATG | 9886 |
rs187456780 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945649 | AAGTCAAAGGCTTGC[C/T]TGGTGCTCTCTAAAT | 9886 |
rs187457525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972464 | ATCGCATGTTCTCAC[G/T]CATAAGTAGGAGATG | 9886 |
rs187477821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980875 | ATAGTAGGAATGCCC[A/G]TTCAAAGAGCCACTT | 9886 |
rs187483764 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960781 | CACCCTTTGATGTCA[A/G]TGGGTGCTGCCTCTT | 9886 |
rs187484159 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941512 | ATTATCAAGCATCCA[G/T]ATCCCCAGTATTCTC | 9886 |
rs187491976 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967748 | CTTTATTCCTTAGAA[A/G]TGATTGCAACCCCAG | 9886 |
rs187492431 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924978 | CAAGTGTTTAGATGA[C/T]GGGGATAGATCACTC | 9886 |
rs187510530 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001079 | GCGCGCGCGCGCACG[C/T]GTGTGTGTGTGTGTG | 9886 |
rs187563961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000195 | TGGGGTTTAAATTGC[A/C]AATACATGAAAACTT | 9886 |
rs187609625 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945800 | CCTAGTCTTTGATAT[C/G/T]AGAAAGAGAGGGTAG | 9886 |
rs187615193 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928459 | TGGATAAGAAATCCT[A/G]TTGTTTGAAACAACA | 9886 |
rs187618531 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914665 | TCATAGCAGCACTGA[C/T]GGAATGGCTGTGTCG | 9886 |
rs187637528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963618 | GGTCATGTGTTCCAT[C/T]GGAACAGGAAAAATA | 9886 |
rs187638729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976609 | GTTTTTAAAACTTCT[A/G]TGCCCAATTAAGTAG | 9886 |
rs187647614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883188 | CAGTGGCTTGGTTCC[A/G]TGGTCTTTGTCTTTT | 9886 |
rs187659182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900587 | TATTAATTTCTCTCT[C/T]ATTGTGCGCACACAG | 9886 |
rs187680301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932440 | TATGTTCAGTTTGCA[A/T]AAAGTCATCAAGCTG | 9886 |
rs187702860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963200 | TGTATGGGTAGGCAA[C/T]TTTCATTGCCCTCCG | 9886 |
rs187708949 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968335 | CAATTCAAAATTCAA[A/G]TGTAGTGTGTAAATG | 9886 |
rs187715264 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900208 | CAAGGTAAGAGTGGG[A/G]GAGGACTGGGAGGGT | 9886 |
rs187718533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907098 | AAGATGTGACTTTGC[G/T]CCTCCTTTGCCTTCT | 9886 |
rs187721689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874730 | CCTTAGGGGACAATG[G/T]GACTGGCATGGGGGT | 9886 |
rs187724487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927251 | CATAGATGGGAAGAT[C/T]GATATTGTTACAATG | 9886 |
rs187769751 | snp | A/C/T | 0.00597598 | 0.0543831 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910417 | CTTTTTAAAAATGAC[A/C/T]TTCTAATAAAAATAA | 9886 |
rs187778382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878470 | ATGGAGCCTAGTTCT[C/T]CAAGATGTCAAAAGA | 9886 |
rs187800835 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002811 | TGCCTTTTAATGAAT[C/T]CTTTCCTTTTCAATA | 9886 |
rs187807217 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886980 | ACCATACTATGATTA[C/T]ACCTAAGAAAATTAA | 9886 |
rs187827700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903495 | ATTACCACCATGTTC[A/G]CCAGTTCCAGAACGA | 9886 |
rs187970293 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879094 | ATTTTACAGAAAAGG[A/T]AATGGAGGTTCAAGG | 9886 |
rs187971267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884094 | CTGAAAAGCAGATAG[C/T]CTTTTGCTGGGGGGT | 9886 |
rs187999498 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982292 | AGGCCTGACTAACTG[C/T]ACTGGGATGGGCTTG | 9886 |
rs188015921 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950845 | TCCCCCAATTCCTCC[C/T]TCCCCAAATGCTGAC | 9886 |
rs188020108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895970 | GTAACTCCTAATTCT[C/T]AACACATCAGTATCC | 9886 |
rs188034611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900885 | TATATTTTAATTATT[C/T]GAATTTCTCTAAAAA | 9886 |
rs188062627 | snp | A/G | 0.00199481 | 0.0315187 | nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60985857 | TACCATATGAAGGGG[A/G]AAAATAAACTTCAAT | 9886 |
rs188066423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929152 | CCCCTCCTTCAACAT[C/G]TGGGGATTATAATTG | 9886 |
rs188068749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954712 | TGGAAGGAAATGTGA[C/G]AAAATTATTTTTGAA | 9886 |
rs188118338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915546 | GTTATTTCATATTTT[C/T]ACCAGTACCCGATGA | 9886 |
rs188128422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901554 | TAGGTAACAGAATTA[C/T]CCACTGAGGATATGC | 9886 |
rs188199281 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988076 | AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC | 9886 |
rs188204619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950642 | AAGAATAATAACTTT[C/T]CAAAAAGTCCTTAAG | 9886 |
rs188207590 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957760 | CCAATGGTAATGATA[G/T]TTATTGAATGCTCAC | 9886 |
rs188209617 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972295 | ACCAACCCAAATGCC[C/T]ATCATGATAGACTGG | 9886 |
rs188216560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887820 | TGAAGGGGAATTGTA[C/T]GCAACAAGCCCACTG | 9886 |
rs188216746 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917941 | TGTATCAATAAAGAG[C/T]TCTAGCAGAAGCAAT | 9886 |
rs188272899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938105 | TTTATGTAACAAAGA[C/T]AGCTTAGAAGGGTGT | 9886 |
rs188339155 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971304 | AAACCATACTACAAG[C/G]CTACAGTAACCAAAA | 9886 |
rs188341087 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946126 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 9886 |
rs188347222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883481 | TCCCTTTGTGCCTGC[A/G]TTCCTGACCTCGATC | 9886 |
rs188355777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915344 | ATAAGTATTATTCAT[C/T]TAACACTATTAATAA | 9886 |
rs188376292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974075 | CATAACATGAAATAT[A/C]ATACTCCTAATATCT | 9886 |
rs188390941 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891872 | CACGGGAGGGACCTG[A/G]TGAAAGGTAACTGAA | 9886 |
rs188409393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941734 | AAGAAACCTGTTCTG[A/G]AATGCATGCTCAAAA | 9886 |
rs188414113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905753 | TAACATCATCATTAC[A/C]ATGTTATTTCTGGCC | 9886 |
rs188465017 | snp | A/C/G | 0.00239401 | 0.0345304 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904836 | TGCTTTTCTTTCATG[A/C/G]CTTTCTACTTTTTTC | 9886 |
rs188491134 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870225 | CTGCTGTCACACTTC[C/T]TAGTTTAACACTGAA | 9886 |
rs188499457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932104 | TTGTTGGTATGCATG[C/T]CATGTATGTATTTGT | 9886 |
rs188503876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996606 | CGAGGGCTGTTGGAA[A/T]GTGCCATGGGGGCAT | 9886 |
rs188541532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993325 | AATGGGTTATTTCAG[A/G]CTCAGCTACAAGGGC | 9886 |
rs188547715 | snp | A/C | 0.115788 | 0.21092 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933496 | GGAGGCTGAGGCAGG[A/C]AGATCACAAGGTCAG | 9886 |
rs188548153 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974495 | AATCAGACTCCAAAA[A/C]ATATACATAGCTAAA | 9886 |
rs188552175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961264 | AGGAAGAACATACTA[C/T]GAGATGACACAGTAT | 9886 |
rs188554065 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920334 | AAACCAAAGGATGTC[A/G]AGAAAAAATAATGGA | 9886 |
rs188635533 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991672 | TCCTGACCTTGTGAT[C/T]CACCCGCCTCAGCCT | 9886 |
rs188645096 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971619 | CTTGACAATACCATT[C/T]AGAACACAGGCATGG | 9886 |
rs188677403 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869766 | CCATCGATAAGATTT[A/C]CAAGCCTATTGAAAA | 9886 |
rs188680551 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956561 | ATTTGGCTTAAAATA[C/T]AAACACATTTAGCTG | 9886 |
rs188686672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937600 | AGAAGCTTGGTATTC[A/G]TTTGCAGCAGAAACT | 9886 |
rs188695302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922873 | TGATTGATCTTCTGG[G/T]GTTAATCCAAGAAGG | 9886 |
rs188696240 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999412 | ATACTTAAAAGTAGC[A/G]TATAAGAAACGGGTT | 9886 |
rs188709340 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978409 | AGGGAACATGGGTTT[C/G]CATTTCTCAATCAAG | 9886 |
rs188727146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875925 | TTCTAGGTCTTTGAC[A/G]TTGATGTCATCTGTA | 9886 |
rs188737394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894079 | AATGAGAAGAGTCAA[A/G]TCGATGAATCAAAAC | 9886 |
rs188755978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908738 | CAGAAAGATGCTGGA[A/G]TGCAAGAGAGAGGAG | 9886 |
rs188793230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955706 | GTCTAAATTTGTGGT[C/T]TACAATGTGTCAGTT | 9886 |
rs188796277 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990549 | CCAGTATTCTCCATC[C/T]GTGCTCAATAAAACA | 9886 |
rs188846292 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003191 | GGTGTTTGGTTCTCT[C/G]TTCCTGTGTTAGTTT | 9886 |
rs188853275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960219 | AAAACTATGATGACA[A/T]TTCTTATACTCTGTT | 9886 |
rs188861951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897423 | TTGACTTTCCTTTTC[C/T]AGTATCATTTATTTT | 9886 |
rs188865261 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983062 | TGCTAGATGGTCTAT[C/G/T]CTCAGTGTTCTTGAA | 9886 |
rs188872914 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924806 | CTTTTCTGACCACAA[C/T]GGAATAAAACTAGAA | 9886 |
rs188877911 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879426 | ATGATAGCTTAGGCC[C/T]GGGCTCAAGCAATCC | 9886 |
rs188887456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60898680 | ATACTTTACCAATAG[C/T]GTGAGGCTTCTTAAG | 9886 |
rs188929232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987276 | TCCCTTAAACGTGGG[C/G]CTTCCACAAGGTTCT | 9886 |
rs189060565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931041 | ACATGAAAAACAAAA[C/T]AAACTGAAAGGAAAT | 9886 |
rs189072135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973494 | TTTCTGAAGGAATTC[A/T]GAAAAAAGTAATTTA | 9886 |
rs189078688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902525 | GTTATTATTCATACA[A/G]GTAATTCACTGTTTA | 9886 |
rs189110704 | snp | C/T | 0.000135867 | 0.00824107 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910862 | TGCATTCAAGCTCAA[C/T]CACGCTGTACTAGTC | 9886 |
rs189148677 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940766 | AGACAAAAAAAATGT[A/G]CTTGGAAATTTTTTT | 9886 |
rs189160536 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977498 | AGACCAAAAAAGATG[C/T]CTCATGATCACAAGC | 9886 |
rs189164440 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894296 | CCACAACAAATAGAG[A/C]AGAAAATCCTGAGAT | 9886 |
rs189164803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923273 | ATAAACATGCTATAT[A/G]AAACAGCAGAAAAAA | 9886 |
rs189166789 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946428 | GGCCCTCATATGTGG[G/T]GGGGCACAGGGCTGA | 9886 |
rs189187299 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977967 | GGAAAGAAATAGATC[A/G]CTTATTAAAGGTTGC | 9886 |
rs189189941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965608 | TAGTATTTCAAGTGC[C/T]TCCATGTTTGACACA | 9886 |
rs189195662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947276 | TAAACATAAAAAATG[A/G]TACCTAAATGGAATT | 9886 |
rs189228148 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998827 | ATAGAAGAACTCTTC[C/T]ACACTTCAGTGCAGA | 9886 |
rs189309216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880526 | CCACTTTCAGACATG[A/G]TTGGTGAAAACGACA | 9886 |
rs189320751 | snp | A/C | 5.61383e-05 | 0.00529773 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911338 | GATGCTGAAGACACT[A/C]TGTGCATCTTACCTC | 9886 |
rs189335801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968821 | TTCTACAGGATGTTC[A/G]CCAAGGCATCACATG | 9886 |
rs189340213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951707 | CATGCTTCTCCATCC[C/T]CATGGTGCTTTGAAT | 9886 |
rs189344248 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932789 | ATAGAGATATACTAA[C/G]CACTCATTTGAGAAA | 9886 |
rs189363951 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982520 | GACTCTGTTGTTGGG[G/T]GCCATCCTATGCATC | 9886 |
rs189369281 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997894 | CTGGGTGGTCCTCAC[G/T]ATTTTTGATCTGAGT | 9886 |
rs189386287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880839 | CATATATGTTTACAT[A/G]CATATGCATTTATCT | 9886 |
rs189397118 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899749 | GACACAAACTGCTGT[C/G/T]CTTGTCACACTTGAT | 9886 |
rs189403520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919211 | TTCCTCCCAAAAGCA[A/T]ATAATCTGAACTTTA | 9886 |
rs189413695 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905363 | GCTGAGGCAGGAGAA[C/T]CACTTGAACCTGGGA | 9886 |
rs189415322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930187 | TTAAGAAAAAAAATG[A/G]AAACAACCTATGACA | 9886 |
rs189440313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876080 | TTCTTTGGCACAAAC[C/G]TCCTCAACTAGATTG | 9886 |
rs189447401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964533 | CCACCTGCTTTGGAG[C/T]CACTCTTGCCAGATA | 9886 |
rs189455347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908983 | TCAAAGGGATAATGG[A/G]TTACAGTTGACAGAA | 9886 |
rs189456890 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003433 | CCTTTGGGTATATAC[A/C]CAGTTATGGGATTAC | 9886 |
rs189467290 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969767 | TTCTAGAGTTGTTTA[C/T]TAGGCATTTATTACA | 9886 |
rs189595733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925490 | AAAAGTAGAAAAACC[C/T]CAAATAAACAACCTT | 9886 |
rs189598207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898955 | GCAATGGCAAAAACC[A/G]CAATTACGTTTGCAC | 9886 |
rs189598653 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965996 | ACAGACAATAAATAT[A/T]TAATTTTAAAAACTG | 9886 |
rs189600451 | snp | A/C/G | 0.00279258 | 0.0372817 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987845 | AAATGCTCTCCACCC[A/C/G]CTAACCCCTGACAAA | 9886 |
rs189631345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931223 | TTCTTTTAAAGTATA[A/C]AATTCAGTGGTGTTT | 9886 |
rs189648043 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973411 | CTTCTTTAAAATTTT[G/T]AGCATAAACTGTATT | 9886 |
rs189651658 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959063 | GAATGCAAAGTTGCC[C/T]CAACGTTCAAAAATC | 9886 |
rs189698407 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952084 | CCCCCAAAAAAGAAC[A/G]GTACATGATAAAACT | 9886 |
rs189740184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983813 | TTGCTACACAGCATG[C/G]ACCCTGCAGAGCTTC | 9886 |
rs189764247 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931414 | ATTCTGGACACTTCA[A/T]ATAAATGGAATCATG | 9886 |
rs189786059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990273 | CAGGCGTCAGCCACC[A/G]TGCCCGGCCAACCTC | 9886 |
rs189805306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886582 | CTTGTTAACATTTTG[G/T]CATGTTTGTTTTACG | 9886 |
rs189824559 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916918 | AGTCAGAGAGAAATA[C/T]GAAGTTGCTATACTG | 9886 |
rs189832520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903476 | CACGTGCATGCTGCC[A/G]GAGATTACCACCATG | 9886 |
rs189846182 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869326 | GCTGCTTTGTTACTG[C/G]AGCATGCACAAGCCC | 9886 |
rs189882684 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971886 | CTGGGAAAAGGATAT[A/G]AACAGACACTTCTCA | 9886 |
rs189886581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948597 | ATGCTGTCATTGGCT[A/G]TTTAGGAGAAATTAT | 9886 |
rs189926307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975539 | CTACTTATTCGCTTG[C/T]ATGGAAATACTAGGT | 9886 |
rs189930066 | snp | C/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996259 | CTAAACCCTTCAGAA[C/G/T]TTAAGACTGTCCACA | 9886 |
rs189941054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919626 | TAATCAACATTATTT[G/T]TTCAATGGACTGTTT | 9886 |
rs189950438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871872 | TGAACCCAGGACCAC[A/C]TGATTTCAGAGTCTA | 9886 |
rs189965863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890329 | AGTCCACAGTCCTCA[A/C]TGCTGCAAGAAAAGT | 9886 |
rs189971856 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951991 | TGAACCCAGGAGGTG[A/G]AGGTTGCAGTGAGCT | 9886 |
rs189997486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962693 | GGTAAAGTCTTAAAA[C/T]AATTTACCATGATCT | 9886 |
rs190063445 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871249 | CAAAAAAAATATACA[C/T]ATCAGTTTAAGGAAT | 9886 |
rs190098114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907815 | GGTAGCTTGGCACAG[C/T]GGAAAGAGTGAGAGC | 9886 |
rs190107375 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895638 | CAAACTCCCCACCTC[A/G]GGTGATCCACCCACC | 9886 |
rs190126692 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936829 | AAATAAAAACTTACA[A/C/T]ATAATCAATTTGAGA | 9886 |
rs190135658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884663 | TAGCCCTAAAAAAGA[A/G]GAAAATTCTGTCATT | 9886 |
rs190138413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924112 | CCAAATCTGTGTATT[C/T]TTTTTCAGTAAAATG | 9886 |
rs190142897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910104 | GGCCATGATATCTAC[A/G]TTCTACACTGAAAAT | 9886 |
rs190144789 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878424 | ATGACAGGTGTTGGG[A/C]GGAGCTGCAAACCAC | 9886 |
rs190162717 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875488 | TGCAGAAAGTTCTAC[G/T]GGATGGAGTGGCTCT | 9886 |
rs190181888 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994586 | TCCCTTCTCTTTTTT[A/T]AAAAAGTTAGATTTT | 9886 |
rs190203900 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905486 | AAAAATTCAAATTAA[A/G]GCAAAAAAATCCATG | 9886 |
rs190238622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933320 | TACCAGTCTGGAGTG[C/T]GACTAGAAATTTTAA | 9886 |
rs190264959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973031 | AATATTTCTAATGCC[A/G]GGGCAACAAAGGCAA | 9886 |
rs190271195 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958865 | CTAGGACTCCCAAAG[A/T]GCTGGGATTACAGGT | 9886 |
rs190273227 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939005 | CTCCACAGAGAGACG[A/G]AACCTGAGATCATAA | 9886 |
rs190339102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922309 | CCCAAAAGAGCCACA[A/C]CACAAAATGCAATTA | 9886 |
rs190368248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893884 | TCATAGGAATTATAA[A/G]CCATCATTCTAGGTT | 9886 |
rs190390947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925777 | TAGAGACCATTATGT[A/G]TAACTATATGTCAAT | 9886 |
rs190407778 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962179 | GGAAATTTTCATAAT[C/G]AGCCACAAATTAGAA | 9886 |
rs190408069 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975395 | ACACTGCCTGCATTT[A/G]CCCTTTTGCCTCTCT | 9886 |
rs190424654 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943278 | ATGGAAACGGTGCAG[C/G]TAACAGTAGGATCTA | 9886 |
rs190426974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961895 | CTCACTGCAACCTCC[A/G]CTCCTGGGTTCAAAT | 9886 |
rs190453354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900028 | CAGAGCAAAGGCCCG[A/G]GGTAGGAGCCTGCCT | 9886 |
rs190461351 | snp | A/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873344 | ATTTATATCATAGAA[A/T]TTGGCAAACGCAACA | 9886 |
rs190479241 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870904 | TGACTTTGTAATTAC[A/G]CCGATGTTATTCAAC | 9886 |
rs190480791 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926002 | TTGTGGGGCCGAGGC[A/G]GGCAGATCACTTGAG | 9886 |
rs190489214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913398 | TATCCTGAACATCCT[A/G]GGTGGGGAAAAAGAG | 9886 |
rs190551865 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993939 | ATATTTGTATATACA[A/C]TTTTAGAGCTGAGGT | 9886 |
rs190608127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876580 | GAATAATTTATAAAA[C/T]CTGTGGATAGTTAGA | 9886 |
rs190618027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894803 | GTATAAAATAGTTCT[A/G]ATTGGTGCCTTCTAT | 9886 |
rs190641049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942446 | AAAATTAGTATATTG[A/G]CTATGATATTCCTGC | 9886 |
rs190654719 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912800 | TACCAGTAGCAGCTG[A/G]ACAGGAGGCCAGCCA | 9886 |
rs190662785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975257 | CAGAATGTGTAAATG[A/G]CTGGTGTTTTTAGGC | 9886 |
rs190683827 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924540 | AGAGACCCTGATATA[A/G]TAAGAGCCAGGGACT | 9886 |
rs190694242 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949047 | GGCTCCAGCTAGTGA[A/T]GACAAACAGGAAAGA | 9886 |
rs190731171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978836 | TTTTAACATTGTCAA[C/T]GTCCCTTTGATTCTC | 9886 |
rs190734297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890147 | AAGACTTTCCCACTT[C/G]TAGTTAAATGATCCA | 9886 |
rs190841194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979839 | AGATTTGAACAAAAG[A/G]CTTCATGGAAGTGAG | 9886 |
rs190843197 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000219 | AAAACTTTAATGGGG[A/G]AAAAGAAATCTACAG | 9886 |
rs190859457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967395 | CCTCCTGGGTTCAAG[C/T]GATTCTTGCACCTCA | 9886 |
rs190902876 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881769 | AAATAGCAAAATGAA[C/T]ATCCTAAATAAAAAG | 9886 |
rs190910245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950108 | ACTGGTCTAGCTCAA[C/T]ATGCATAAGAGGAGG | 9886 |
rs190917909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931555 | TTCTTAGACATATTA[C/T]TTCTATAATGAGAAA | 9886 |
rs190930548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917169 | GCAATAAGAAACTAA[C/T]GTAGCACACTTTAGC | 9886 |
rs190940117 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910547 | AGTGCCAAAATAACT[G/T]AAAACATTCTAACAG | 9886 |
rs190961290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999858 | AACCGTAAGGTAAAT[A/G]CCATTTCATATACAG | 9886 |
rs190970939 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939733 | AAAAGGAAGACCAAG[C/T]GACAGTTTTAAACAT | 9886 |
rs190975323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966735 | GGTACATGTGCACAA[C/T]GTGCAGGTTTGTTAC | 9886 |
rs190980680 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971349 | TACCAAAACAGATAT[A/G]TAGACCAATGGAACA | 9886 |
rs191039152 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882833 | TAACTTAGAGCTTTC[C/T]GGGGACAAATACCCT | 9886 |
rs191040435 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913741 | CCAAATGTTACAGGG[C/T]TGAGGTTGTGAAACC | 9886 |
rs191049172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900425 | TCAGAATAATGATAA[A/G]CTTTTTCGTGAGCTA | 9886 |
rs191064480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914124 | AGCAGTAACTCACTG[A/G]AAATTAAAGAATACA | 9886 |
rs191064774 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952331 | AGTATGGGACTAGTG[A/C]ACATGATAATAATAA | 9886 |
rs191066599 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933940 | GCCTAAATACACACA[A/C]AGAGATTGAGATATA | 9886 |
rs191073230 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945016 | CAGAAACTTCTCTCT[C/T]TTCCAGGCTGACCGT | 9886 |
rs191077208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920465 | AGGCCTGAAGAGCCC[A/G]AGGGATAGGAAGTGG | 9886 |
rs191186734 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984209 | AGTTAAAAACTGACA[C/T]GCAAAATCAAAGCAA | 9886 |
rs191194599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903034 | ATACAGTTATTGCTA[C/T]GATAGGGATTTGCAA | 9886 |
rs191198323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970665 | ACGTTACCAAACAAC[A/G]TAAGACTCAAATACT | 9886 |
rs191212945 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932455 | AAAAGTCATCAAGCT[A/G]TACATTTGCGATCTG | 9886 |
rs191216904 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918807 | CTGGAGTGCAATAGC[A/G]CAATCTTGGCTCACC | 9886 |
rs191217036 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870618 | CAGAAGCATGGCAAG[C/T]TCAAGGAATACTGAG | 9886 |
rs191227160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905247 | CAAGGTCAGCAGTTC[A/G]AGACCACCCTGGCCA | 9886 |
rs191227282 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889867 | GTATTTTGTCGACAG[C/T]AAGTGCCTGATAAAT | 9886 |
rs191267666 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986380 | TGAGGTGCTTTCCAA[G/T]AAATTAATGAAATAT | 9886 |
rs191308807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900107 | TCGTGAGGGGAAACT[A/G]AAGTCTTTGAGCAGA | 9886 |
rs191321934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927101 | TGAAAAAGAAATCAA[A/G]AAAGTAATCCAATTT | 9886 |
rs191353290 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951315 | CTTTCCTTAATTGGC[A/T]CCACCACTCCTTTCA | 9886 |
rs191371561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989509 | TCTCTCTCCAGTTGC[C/T]CGCTAATCTCTCACT | 9886 |
rs191425464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916733 | GTCCACGGAATCCGC[A/G]GAACTTGTGAATATG | 9886 |
rs191448746 | snp | A/G | 0.000231298 | 0.0107515 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886108 | CTTTTAGGAAGGCAC[A/G]TACCTCACTGTTGGC | 9886 |
rs191494601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954876 | AAATGGTCAAGTTTC[A/G]GAAATAGTTCATATT | 9886 |
rs191495523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921290 | ATATCACTGAGACTG[C/T]TGTATGTACAGAGAA | 9886 |
rs191507567 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993495 | GCAAGGCATAACTGA[A/T]TTTTTTCTCCTTTGC | 9886 |
rs191514355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985538 | TGTACAAAATGCTAC[A/G]CACTAAAGAATTTTA | 9886 |
rs191527149 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954352 | TATAAAAATACAGAA[G/T]ATATAGCAGTCTCAA | 9886 |
rs191549462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892349 | CTTGAGAATGAAATA[C/T]TGTAACAGGTTGGAC | 9886 |
rs191556279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934841 | TAAAGAGCCAGGAGA[A/G]CATACTTTAATGAAT | 9886 |
rs191560437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921665 | TTGTTGAATTGAATA[C/T]AAAAATACAGCCACT | 9886 |
rs191566018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873884 | CACGGCCTTTGCCTA[A/G]GGCGGTGCCTGGTAT | 9886 |
rs191569440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906867 | CAAAAGGGACTGATA[C/T]GGTTTGGCTGTGTCC | 9886 |
rs191576670 | snp | A/G | 0.000627943 | 0.0177081 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892796 | ACAGGGAAACACTGA[A/G]TCCCTTGGCTTACCT | 9886 |
rs191737361 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934544 | ATGTCAGAAGAGAGT[A/C]CCTGGTCTACTTCAA | 9886 |
rs191753699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997257 | GAAATTAAAAAGATA[C/T]CAAAATTGTGATTGG | 9886 |
rs191759863 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906293 | AAGGACTCATGCTCC[A/G]CTACTTAATGGATGC | 9886 |
rs191781603 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971249 | CAAGATAATCCTAAG[C/T]GAAAAGAACAAAGCT | 9886 |
rs191838373 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938731 | TGTTGTTTTTTTGGA[G/T]GGGGGGTTTGTTTAG | 9886 |
rs191853417 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909608 | AAGCAGGTTCATTTA[C/T]AATTGTTATTTTTAC | 9886 |
rs191859804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972489 | GAGATGAACAATGAG[A/G]ACACAGGGACACAGG | 9886 |
rs191862995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992118 | AAAAATCCAACTCAG[A/G]ATTTTTAAATCCTGG | 9886 |
rs191869077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887242 | AAGACTGTTTCTGTA[A/G]CACAATGGCCAGTGT | 9886 |
rs191876629 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001244 | CACCCTCCTTTCAAG[G/T]GTGCAAAGGGATGCT | 9886 |
rs191878486 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961043 | GTCAACTGTGCTTTA[C/T]CCAGCCCCTCTTTTT | 9886 |
rs191880073 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974155 | TATAATCAGTTAAGA[A/G]TGTTGTCACCCCTCT | 9886 |
rs191901969 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911250 | AAGGTTAGTTTTGTT[A/T]TGAATGTGTAATTTA | 9886 |
rs191938941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941572 | TGAAAAATAAAAAGT[C/T]GTATGATGGACAAAC | 9886 |
rs191943313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898833 | TTTAAACCAGTCTTC[A/C]ACCACCCTCTGAAAG | 9886 |
rs191945994 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925117 | CTCCCTATTGCTCCT[C/T]CTCTGGCCATGTGAC | 9886 |
rs191966822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906281 | TACTGAAAGCAAAAG[G/T]ACTCATGCTCCGCTA | 9886 |
rs191987713 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872891 | AAAAAAGACTAGATC[C/T]TCAAAAATCAACTAT | 9886 |
rs192085562 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945906 | ACTTCCCGGCCCAGG[C/T]GGGTGGCTCACGCCT | 9886 |
rs192090347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963275 | ATAATTTTGATGTCA[C/T]CAATCTTTTTCTTTG | 9886 |
rs192095409 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928686 | AAATACAGTTACATA[C/G]AAGGAGTAAGATCTA | 9886 |
rs192100581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900820 | TTAATGCTGAAAGAC[G/T]GCCATGTAATACCTC | 9886 |
rs192103648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914889 | GTGACTGCCAAAGGT[A/G]CTGACCCTTGTGCAA | 9886 |
rs192105468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875580 | CCCCACTCACATCAC[C/T]GCAATCCTTAATATC | 9886 |
rs192108366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927280 | TGCCCATACCACCCA[A/G]TGCAATCTACAGATT | 9886 |
rs192115686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996496 | TGAGGAATTTGCCTC[A/G]CTGTCCACCATTGTA | 9886 |
rs192141529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903961 | CCATAAGGATATTTC[C/T]TTTCTTTTCTTTTTT | 9886 |
rs192145807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923698 | GTTGTGAGAGGGACC[C/T]AGTGGGAAATAATTG | 9886 |
rs192161989 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869942 | AGATTTTCAAATGCA[C/T]ATGGCTGTCAGCATT | 9886 |
rs192170782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988718 | CACTGATGGGCACCT[A/G]GGTTGATTCCATGTC | 9886 |
rs192185118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958049 | CCACAGTTAATCTCA[G/T]TAAAAAGCCAGTAAT | 9886 |
rs192228536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976640 | ACATTGTCCAACAGA[C/T]CCGATAGGAAATCAC | 9886 |
rs192231233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963625 | TGTTCCATTGGAACA[A/G]GAAAAATATTTCAGA | 9886 |
rs192250455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896964 | CTTCAGATTTTAAAC[A/G]AACAAAAAAAAGCAT | 9886 |
rs192323880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968963 | CTAATGCTGATGCCC[A/G]TGTTCTTGTTATTGT | 9886 |
rs192331335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892179 | CCACCAAAATCAATA[A/T]CGACATTTTATATAT | 9886 |
rs192339666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951764 | TGGTTGTTAATAATG[A/G]TAAATGGTTGTTAAT | 9886 |
rs192342760 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932918 | CTCTAAAGATGTTAC[A/C/T]GAGTTAGCTTCTGAA | 9886 |
rs192376998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982333 | GACAGTACTCAGTAC[A/G]GATACCATTTAGGTG | 9886 |
rs192395537 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879187 | CCAGGGAGTATGATG[A/C/T]GAAAGTGTATGTTCA | 9886 |
rs192405274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897900 | TAGTAGAGATGGGGT[G/T]TCACCATGTTGGCCA | 9886 |
rs192421207 | snp | C/T | 0.00496383 | 0.0495709 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910865 | ATTCAAGCTCAACCA[C/T]GCTGTACTAGTCTTG | 9886 |
rs192457090 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982793 | CATAGTAAGTTACAG[G/T]GCTAGAATGCATGTA | 9886 |
rs192462399 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945704 | GGAATCCAATGTTTT[A/T]ACGAGGAAAGTTATC | 9886 |
rs192463943 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002937 | CTTCTTCTTCTTATT[A/C]TTATTATAATACTTT | 9886 |
rs192513814 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976225 | AGGATATTTTATTAC[A/C]TGGAAGGATTTTTTA | 9886 |
rs192526596 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946412 | AATCAACATGTATCA[C/T]GGCCCTCATATGTGG | 9886 |
rs192541820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915460 | AAAAAAAAAAGAAAA[A/G]CCTGAAAGAATGGAC | 9886 |
rs192550046 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977317 | GAGAAATAATGCCAA[C/T]GACAGCTTCATGGGG | 9886 |
rs192583605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883526 | CTGTGAATAGCAGGT[C/T]CTCTGCTGCACAATC | 9886 |
rs192619742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986743 | GGCAAAACAGTACTT[C/T]TGCTTGGAGGTAGTT | 9886 |
rs192686624 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971574 | GACTTAAACATAAGA[C/T]CTAAAACCATACAAA | 9886 |
rs192700844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878532 | GACCAGCTTGATTTC[A/G]AAATTCTGTCAGTAT | 9886 |
rs192701526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935316 | TCAAGATAAGGGTTA[C/T]ATTGATTGGGTAGTG | 9886 |
rs192744961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968559 | TGCTGACCATCTTTG[A/G]GGAGCTGCAGAAAGC | 9886 |
rs192764398 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002561 | AGCTTGCGTAATGAA[A/G]GGCTAGAGATAGCTA | 9886 |
rs192784414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932343 | GAGGTGTTTCAAACA[C/T]ACTGAGGGTGGAGTG | 9886 |
rs192791507 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904861 | TTTTTCTATAACCTG[A/G]GCAATTTTTAGTTCT | 9886 |
rs192799622 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968002 | CTGGAGGGAAAGAAG[A/G]GAGCAGAGGGACTGC | 9886 |
rs192820529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929393 | AAATTGATATTTATA[C/T]GAAAGCAACATAAAG | 9886 |
rs192833840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964361 | CCTCTAGGGGACACA[C/T]GGAAAATAAGCAAAG | 9886 |
rs192852560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900929 | ATGTAATTGGATAAT[C/T]TCATAACATCAGAAT | 9886 |
rs192921228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888157 | CTCATGTCTGGCTAA[C/T]GTTCAATGAAACACA | 9886 |
rs192933784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956058 | CTTAGGCAATTTCAT[C/T]GTTGTGCAAACATCA | 9886 |
rs192939247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922616 | CCATAATCTGGAGTA[A/G]TGAGAGCCACACTGA | 9886 |
rs192949459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987596 | TGTAGGCAATGACCT[C/T]TCATCTAATGTGTTC | 9886 |
rs192995697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918027 | CAAATCATGGAATGG[C/T]AGCTTGTGAATCTGT | 9886 |
rs193004934 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981064 | AAATATCCTTACTGG[A/G]AAATTCTATGTTTGA | 9886 |
rs193005694 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919431 | TTTAATCAGCAGTTG[C/T]AGGTAGGTGGGAGCT | 9886 |
rs193009599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940855 | AAATGTACCATTGAT[C/T]CCCAATTCAGCCTTC | 9886 |
rs193009970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950734 | TCATAAGTGTAAAAA[C/T]GGGCTCATTATGAGG | 9886 |
rs193021790 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973507 | TCTGAAAAAAGTAAT[A/T]TAGGGATTACATCAT | 9886 |
rs193076305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883308 | AGGTGGCCTCCTCCA[A/G]GAGAGGCCATCAAAC | 9886 |
rs193076369 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907858 | AGAGTGGCTTTGAAT[C/G]TGCCTCTGAGACTCA | 9886 |
rs193102817 | snp | A/G | 0.00278668 | 0.0372233 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874987 | AGAGAGCACTTCTCC[A/G]TCAATGCCCACGCCA | 9886 |
rs193126513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964651 | TGACTAATGTGTTAG[C/T]CATTGTTTAGACTTT | 9886 |
rs193135818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998082 | TCAGTTTCCTCTGCC[A/G]TAAAATATGGGGTTG | 9886 |
rs193141425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907442 | TATGTATGGTTTTGT[C/T]CCTGACATTTTAAAA | 9886 |
rs193171665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937385 | ATACTCAATACTACA[A/G]TGAATTGAAATGAAG | 9886 |
rs193177428 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971754 | TCAACAGAGTGAGCA[A/G]GCAACCTACAGAATA | 9886 |
rs193204844 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960507 | TGTACCAAATAAATG[A/G]CTGTTTTGTCTGAAA | 9886 |
rs193207986 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905404 | GCAGCAAGCCAAGAT[C/T]GCGCCACTGCACACC | 9886 |
rs193208938 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924861 | AACTTTATGAACACA[A/T]GGAAATCAAACAATA | 9886 |
rs193211370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991576 | GCTGGGATTACAAGC[A/G]CATGCCACCATGCCC | 9886 |
rs193280885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977707 | CCCACATGAACCAAG[A/G]TGGTGAAAAAGGGAT | 9886 |
rs193284111 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946502 | ATGAGGCAGATGCTA[C/T]AATTATCCTAATTAT | 9886 |
rs193292001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921954 | CACCCTTTCACCAAA[G/T]GGGAAGGTGGTGGTG | 9886 |
rs193297565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893553 | CCACTTATCTGTTTC[C/T]GAAAAGAAAAATCCT | 9886 |
rs199524926 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875048 | GCATGCTGTTCTGGG[A/G]AAGAGAGAGGGGGCA | 9886 |
rs199594419 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920146 | ACTCACCTGCTGAAA[-/T]TTTTCTCACTAAGGC | 9886 |
rs199608904 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896987 | AAAAGCATTTTTTTT[-/C]AGTTATCTTTCGAGG | 9886 |
rs199623717 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903780 | TATGACAGTGTCCCA[C/T]CGTTAGTTTCAGGGT | 9886 |
rs199707547 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953980 | TTAAATTTACTTTAA[C/T]TCTATTCCATGTTAT | 9886 |
rs199713245 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942991 | CAAGGCTCAGTGAAC[-/A]AGCACAGGATGGGGA | 9886 |
rs199737157 | snp | A/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872204 | AGATTTTGATTTGAT[A/T]TCCTTACGGAACTTG | 9886 |
rs199764972 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979840 | GATTTGAACAAAAGA[C/T]TTCATGGAAGTGAGA | 9886 |
rs199771269 | in-del | -/C | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001317 | GGGTGGGCAGAGAGA[-/C]CCCCCCATAATCCCG | 9886 |
rs199774362 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886727 | AGATGTGGGGGGGGG[-/T]GGGTCTGGCTATGTT | 9886 |
rs199788156 | in-del | -/AAA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951903 | CTCTACTAAAAATAC[-/AAA]AAATTAGCCGGGCAT | 9886 |
rs199887250 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951912 | AAATACAAAAAATTA[A/G]CCGGGCATGCTGGCA | 9886 |
rs199937590 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912194 | ATTCATAAATATATA[-/TG]TGTGTGTGTATATAT | 9886 |
rs199974431 | snp | G/T | 0.00175508 | 0.0295713 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910881 | GCTGTACTAGTCTTG[G/T]TTTACCTGCCATATG | 9886 |
rs199994411 | snp | A/G | 3.30262e-05 | 0.0040635 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875006 | ATGCCCACGCCACTC[A/G]TGGCGGCTTTGGTCA | 9886 |
rs200075471 | in-del | -/CT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880176 | GATACTGAGGGATGA[-/CT]CTGTGTGTGTGTGTG | 9886 |
rs200091850 | snp | C/G | 4.9826e-05 | 0.00499104 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888699 | GTCGACACTCAATAT[C/G]CGCCCCTGGAAATCT | 9886 |
rs200154803 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886189 | AGATCAGCAGCGGCT[C/T]GTGGGCACTGATGGC | 9886 |
rs200182347 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878627 | TGGATTCAGAACTAC[C/T]GGAACGTTATCAGTT | 9886 |
rs200219542 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927983 | CAAACAACTCAACAG[-/A]AAAAAAAATCCAATT | 9886 |
rs200229353 | snp | A/G | 1.6628e-05 | 0.00288335 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911569 | TGTAAGAAGAGAGTG[A/G]ACACCACAGTAAGGA | 9886 |
rs200251257 | in-del | -/ATCAGTCCTC | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946315 | TGTTCACTCCTAGCA[-/ATCAGTCCTC]TTCATTACAAGCTAT | 9886 |
rs200283256 | in-del | -/A/TA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895399 | GTTAAAAATAAGATT[-/A/TA]ATTTTTTATTTATTT | 9886 |
rs200317222 | snp | C/T | 4.96298e-05 | 0.00498121 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878037 | CTTGCATTGATATCT[C/T]GTTTATGTTCGGGAG | 9886 |
rs200321800 | snp | C/T | 0.000319534 | 0.0126359 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888634 | TTTGAAGACTTCCAC[C/T]GGTCGGCCTGAGGAA | 9886 |
rs200327447 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985625 | TAGGTCCAAATGACT[-/C]AAATTCTAAACCAGA | 9886 |
rs200381691 | snp | C/G/T | 6.69495e-05 | 0.00578542 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888551 | ACCCCTTACTCCATC[C/G/T]GGTCAAAGTCTGTGT | 9886 |
rs200385301 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895407 | ATAAGATTATTTTTT[A/T]TTTATTTATTTTTTG | 9886 |
rs200391093 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874859 | GACTCAGTGGTGACA[-/T]CTTCATTTAGACAGA | 9886 |
rs200466425 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879511 | CTAATTTATTTTATT[-/A]ATTTTTTTTTTTTGT | 9886 |
rs200506901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966190 | AAAAACTTTTAATAT[C/T]AGTTTTCTCTGATGT | 9886 |
rs200539529 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960452 | AATGGCCCCTTAGAG[A/G]ACTAGAAATTTAATA | 9886 |
rs200552263 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002919 | TTCTTCATTTCTTTT[C/T]TTCTTCTTCTTCTTA | 9886 |
rs200567806 | in-del | -/GA | 0.0178098 | 0.0926698 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996553 | TGACCTGATGTCCCC[-/GA]GAGCTTCGGCAGCCT | 9886 |
rs200595648 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001078 | TGCGCGCGCGCGCAC[A/G]CGTGTGTGTGTGTGT | 9886 |
rs200598368 | snp | A/G | 0.00155789 | 0.0278661 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872139 | GATAAAAGCTTCCAT[A/G]AGAGGTGAGGAGAGC | 9886 |
rs200599538 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951910 | AAAAATACAAAAAAT[A/T]AGCCGGGCATGCTGG | 9886 |
rs200600876 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888869 | GGATGAACAGAACAT[C/T]GGCACATAGAGGATT | 9886 |
rs200609962 | snp | A/G | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882431 | TGAGTACCTCTGGGG[A/G]GAGAATTATGCTTAC | 9886 |
rs200613802 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869634 | TGGCAAGATTACAAT[-/C]CAAATGGGAGCTTTG | 9886 |
rs200635439 | in-del | -/TTTG | 0.0150606 | 0.0854603 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947587 | TTGAGATTGACTTTT[-/TTTG]TTTGTTTGTTTTTTT | 9886 |
rs200718459 | in-del | -/AAAT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951906 | TACTAAAAATACAAA[-/AAAT]TAGCCGGGCATGCTG | 9886 |
rs200772918 | in-del | -/C/TTTTTTTTTTTTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955046 | TTTCTTTCTTTCTTT[-/C/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 9886 |
rs200799219 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933203 | CTAGTATTTTTCAGG[A/G]CATGTTCCTATACCT | 9886 |
rs200850462 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953981 | TAAATTTACTTTAAC[C/T]CTATTCCATGTTATT | 9886 |
rs200856921 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991484 | CACGCAGGCTGGAGT[G/T]CAGTGGTGCAATCCT | 9886 |
rs200937300 | snp | A/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942859 | ACCACCGATAACGGT[A/T]TTTTTTTTTTTTTCT | 9886 |
rs200950035 | snp | C/G/T | 0.000170553 | 0.00923325 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888213 | CGCGGCCCACTCACC[C/G/T]GAGAACGTTCCCTTG | 9886 |
rs200984963 | snp | C/T | 6.64286e-05 | 0.0057628 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888700 | TCGACACTCAATATC[C/T]GCCCCTGGAAATCTC | 9886 |
rs201003285 | snp | A/G | 0.00046307 | 0.0152092 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874948 | AAAAAGCAAACTGTT[A/G]CAAACCTGAGCCAAT | 9886 |
rs201027917 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882216 | CTTAAAAAAAAAAAA[-/AG]AGTGATCAAAGAGAA | 9886 |
rs201028853 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953773 | AGGTGGCTAATGATG[-/A]AAAAAAAAAGCATAT | 9886 |
rs201036461 | in-del | -/ATT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915618 | TTTGAAAAATTGTTA[-/ATT]AATAAACAAGACAGT | 9886 |
rs201037236 | snp | A/G | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888445 | GTCCGAAAAGGGCCT[A/G]GCTGGACTGAAGCGT | 9886 |
rs201102597 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880806 | TAGCACCAGTTACAC[-/T]GCGTGTATGCTCGCA | 9886 |
rs201104696 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887255 | TAACACAATGGCCAG[C/T]GTTTGAAGTAAATAC | 9886 |
rs201168820 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985233 | TTATGGGTGGACAAA[A/G]GAGAGTAAACTGTCC | 9886 |
rs201188094 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919333 | TATATTATTGACAGG[-/A]AAAAAAGGAAAATGT | 9886 |
rs201204846 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997675 | GAATTGGTAAACTAA[C/T]GATAAGTATTAAAAG | 9886 |
rs201210194 | snp | C/T | 0.000168438 | 0.00917555 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888609 | CCCCAGAGCCTCCAC[C/T]AGGCTCTTGTTTGAA | 9886 |
rs201223079 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895400 | GTTAAAAATAAGATT[A/T]TTTTTTATTTATTTA | 9886 |
rs201230205 | snp | A/G | 0.000346738 | 0.0131624 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892851 | AACAGCTTCCAGGTC[A/G]GCATAGCGGAGATCA | 9886 |
rs201244986 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973091 | TAGTATGTCTGTTAA[-/T]TTTTTTTTATGATTT | 9886 |
rs201249497 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947590 | AGATTGACTTTTTTT[-/G]TTTGTTTGTTTTTTT | 9886 |
rs201334686 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953982 | AAATTTACTTTAACT[C/T]TATTCCATGTTATTG | 9886 |
rs201334720 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927763 | AACGATGAAACGATT[A/G]TAAGAAAATATTGAG | 9886 |
rs201354939 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886171 | CCATCCACTCACAGC[C/T]ACAGATCAGCAGCGG | 9886 |
rs201355999 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951913 | AATACAAAAAATTAG[C/G]CGGGCATGCTGGCAG | 9886 |
rs201385892 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910734 | CAGGAAACAATACCA[-/T]TTTTTTTTTCTTTTC | 9886 |
rs201417955 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968155 | CAATTCAAATGTAGC[-/T]CCATCTGCACCTCTA | 9886 |
rs201419173 | snp | A/C/T | 8.9621e-05 | 0.00669346 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889205 | AATAGAACATTTTAA[A/C/T]AATTATAATCAGCCT | 9886 |
rs201420081 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962770 | TTTTTAAAATGTTCT[A/G]ATTTCTGGTCCCATC | 9886 |
rs201431886 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882018 | ACTTTTGGAACATGC[A/G]TTTTTTCCCCTCATG | 9886 |
rs201467719 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951345 | ATAATGGTTCCTAAT[C/T]TAAAAGCAAAGATGA | 9886 |
rs201482523 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951911 | AAAATACAAAAAATT[A/C]GCCGGGCATGCTGGC | 9886 |
rs201494099 | snp | C/G | 0.000132673 | 0.00814363 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871661 | GGTTGTCTGGTGAAG[C/G]AAAGATGCAGACCAT | 9886 |
rs201499193 | snp | A/G | 6.68717e-05 | 0.00578199 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888658 | TGAGGAATCCTAGGC[A/G]GGCCCTCCTCCCTTT | 9886 |
rs201545300 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896399 | GAAATGACCTCAGGG[A/G]TCCTGTTTCAGCTGT | 9886 |
rs201622377 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947582 | TGTTTTGAGATTGAC[-/T]TTTTTTTGTTTGTTT | 9886 |
rs201634594 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909177 | ATCTATGAAGGCCAT[C/T]GTGCCATTAAATAAA | 9886 |
rs201706826 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953979 | TTTAAATTTACTTTA[A/T]CTCTATTCCATGTTA | 9886 |
rs201735074 | snp | C/T | 7.00501e-05 | 0.00591778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892793 | AGGACAGGGAAACAC[C/T]GAGTCCCTTGGCTTA | 9886 |
rs201736734 | in-del | -/G | 0.078151 | 0.181571 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880131 | TTGGCTGTCTGAGTT[-/G]GGGGGGTGGTCCTGG | 9886 |
rs201739634 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951913 | AATACAAAAAATTAG[-/C]CGGGCATGCTGGCAG | 9886 |
rs201792671 | in-del | -/T | 1.69502e-05 | 0.00291115 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871463 | GGTTTCTGTTTTTTG[-/T]TTTTTTTTCTCTTCC | 9886 |
rs201830250 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905572 | GTGTCTGAGGCAGAA[-/G]GGAAAAAAAAACCAA | 9886 |
rs201848680 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895406 | AATAAGATTATTTTT[A/T]ATTTATTTATTTTTT | 9886 |
rs201889243 | snp | C/T | 0.000148705 | 0.00862151 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875031 | TGGTCAACTCCTGAA[C/T]GGCATGCTGTTCTGG | 9886 |
rs201893242 | snp | C/T | | | splice-acceptor-variant | RHOBTB1 | GRCh38.p7 | 10:60889186 | CCTCTCTTTATGGGC[C/T]TGAAATAGAACATTT | 9886 |
rs201980179 | snp | A/C/T | 0.000115447 | 0.00759679 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888823 | GTAGCGAGGTAAATT[A/C/T]GATGTGCAAAGATGT | 9886 |
rs202012824 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985235 | ATGGGTGGACAAAGG[-/A]GAGTAAACTGTCCAT | 9886 |
rs202016103 | in-del | -/TGA | 0.0138799 | 0.0821421 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966200 | AATATTAGTTTTCTC[-/TGA]TGTTAGGATTATGAG | 9886 |
rs202042890 | snp | A/G | 3.32215e-05 | 0.00407549 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888695 | CTGGGTCGACACTCA[A/G]TATCCGCCCCTGGAA | 9886 |
rs202055400 | snp | C/T | 3.32176e-05 | 0.00407526 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886234 | TAAATGTCACGTCTG[C/T]CAAGGGATTGAGGAA | 9886 |
rs202064331 | snp | A/C | 9.88533e-05 | 0.00702971 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888926 | TCCCCATGGAAGGAC[A/C]CTCTGGAATTTTGAT | 9886 |
rs202066601 | in-del | -/CCC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881015 | ATAGCTCCCATAATT[-/CCC]ACGTGTTGTGGGAGA | 9886 |
rs202096695 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000000 | TTGTTTAATTGACAG[A/G]AAACATGCATCTAAA | 9886 |
rs202217165 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895307 | CTATCTGTATATCAG[-/A]AAAAAAGGTCTTCTT | 9886 |
rs202222589 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947302 | GAATTCAAGCAACAT[C/T]GTATCTTTAAACACT | 9886 |
rs202231960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911323 | ATGATGTGCCCTAGG[G/T]ATGCTGAAGACACTC | 9886 |
rs207471040 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895245 | AAAAGAGGTTGTGCT[A/G]AGAGCAATACTACCT | 9886 |
rs207471041 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924895 | TCTTAGATATAGTTT[A/G]GGTACTTTTCCCTGA | 9886 |
rs367554429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906934 | ACATGTCGTGATGTC[A/G]TGGGAGGGACCCAGT | 9886 |
rs367585941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957378 | GTGTTCAGATGGCTG[C/T]AATGTCACTAGGCAA | 9886 |
rs367604975 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999936 | GGAGAAATTTTATTT[C/T]AAAGTTTCATAGGAT | 9886 |
rs367612972 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944872 | CAGGGGGCGTAGGGA[C/T]GCACCGCTGACCCCG | 9886 |
rs367619145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998238 | TTCATTTAGGCTTTC[C/T]CAAGGAAGGGACAAT | 9886 |
rs367628521 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902041 | ATTTGGCACTCCGCT[G/T]TCCAAGGACAATTTC | 9886 |
rs367640445 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894010 | AAATTCAGAAATAAA[C/G]TCTTACAATTTCATT | 9886 |
rs367645559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898004 | CCACCGCGCCTGGCC[A/G]CTAATAATTATATTT | 9886 |
rs367664386 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910845 | GGTTTTGAAAAGGAA[A/G]TTGCATTCAAGCTCA | 9886 |
rs367705019 | in-del | -/CTT | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000283 | CATTTTTGATACCTA[-/CTT]CTTCTCACCAGAGAC | 9886 |
rs367709328 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955682 | TCAGTGTAAGAAAGC[A/C]TTCCCTTAGTCTAAA | 9886 |
rs367719307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963135 | AACAAACCACACCAT[C/T]TGGTTTGACCAAAAG | 9886 |
rs367727205 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940784 | TGGAAATTTTTTTCA[C/T]GCATATATGGAATTG | 9886 |
rs367732880 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876502 | GATCACAAACCTTGT[A/T]GGGCAGATTTGGCTC | 9886 |
rs367780179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951600 | TTGTAAACATAAGCC[A/G]ATGATTCCAGGGATC | 9886 |
rs367801922 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957184 | TACAAACAGGAGTAC[A/G]TTCTAAAATAATGAC | 9886 |
rs367853412 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902383 | CCTTTAATTGTTCTA[A/C]TTAATGCTCTCATCT | 9886 |
rs367884431 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924739 | CAAGGATAGACCATA[C/T]GTTAGGCCACAAAAC | 9886 |
rs367901643 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889054 | GAAATCAGCGCTGCT[C/T]GGATTGCATTGTCAA | 9886 |
rs367925354 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934292 | TTTTCAGTCCTGAGC[A/C]GACGTCCCACTCATC | 9886 |
rs367946020 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894490 | TTGTCTTTGGGATTC[G/T]GATTTACTTAGTGAA | 9886 |
rs367975575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961020 | TCTATCTGTACTGTA[C/G]TCAGAGAGTCAACTG | 9886 |
rs367989491 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990186 | GTCGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 9886 |
rs368040958 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967389 | TCTCCACCTCCTGGG[G/T]TCAAGCGATTCTTGC | 9886 |
rs368054994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997347 | ATGCAGTTGTGTGGG[A/T]GCAATCTCAAACCTA | 9886 |
rs368088716 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872304 | AACTGCAGAAAAGTG[A/G]GCAAAAGGAGGGTAA | 9886 |
rs368109084 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934703 | CAAATTTAGCCTTTG[A/G]CTCCATGTCCACTGT | 9886 |
rs368213517 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990204 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9886 |
rs368228845 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876605 | GTTAGATGGCTTGGA[A/G]CTCATGTTTCTGAAA | 9886 |
rs368269617 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955371 | TTTATGGTTTTAAAA[-/C]TGCCACAATTCAATT | 9886 |
rs368291527 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888024 | CTGCAAAATGGAGAC[A/G]ATCATATTTAACCTT | 9886 |
rs368303011 | snp | A/G | 4.99754e-05 | 0.00499852 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886246 | CTGCCAAGGGATTGA[A/G]GAAACACAACCATGA | 9886 |
rs368342771 | snp | A/T | 1.77634e-05 | 0.00298017 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892783 | TAACTTGGTCAGGAC[A/T]GGGAAACACTGAGTC | 9886 |
rs368344760 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875920 | AGCATTTCTAGGTCT[G/T]TGACATTGATGTCAT | 9886 |
rs368355894 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968301 | GGCATGTGGTCAGGT[A/G]TAGGAGTGTTCCTTT | 9886 |
rs368405008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899334 | ACTCTCTTTCAACTC[C/T]GTCTGGAGTTCATAT | 9886 |
rs368439347 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990504 | TTAGCAATTTCTCTT[C/T]ATTTTAATTCAAAAA | 9886 |
rs368443238 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919388 | CAACAGCCAAGTTTC[A/G]ATTGTGCAGATTTCA | 9886 |
rs368468916 | snp | A/C/G | 0.000890665 | 0.0210849 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911021 | AGAGCATCTGTGCTC[A/C/G]GTGTCAGTCAGAAGT | 9886 |
rs368469750 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982330 | GTTGACAGTACTCAG[G/T]ACGGATACCATTTAG | 9886 |
rs368477431 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878863 | TGGAGATGTACACTG[C/T]GTAGCAGCTACTCTT | 9886 |
rs368506260 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917933 | TTTTTCTCTGTATCA[A/G]TAAAGAGTTCTAGCA | 9886 |
rs368573726 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903031 | GCAATACAGTTATTG[A/C]TACGATAGGGATTTG | 9886 |
rs368599418 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944384 | ATTTCATTCATGAAA[C/G]CGGGGCCTGGTGTGT | 9886 |
rs368615201 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891855 | CCATAATCCCCATGT[A/G]TCACGGGAGGGACCT | 9886 |
rs368628293 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915605 | AAGGGACAAGCTTAT[C/T]TGAAAAATTGTTAAA | 9886 |
rs368637491 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997779 | GTTATACATACTAAG[A/G]TGTTCTAATGCTGCT | 9886 |
rs368653048 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985958 | AACCTAGGAAAGAGA[C/T]ATATACAAGCATGGA | 9886 |
rs368653881 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881517 | AAAACAATGCCTCTC[A/G]TGATAGCGCAAGAGC | 9886 |
rs368669641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996562 | GTCCCCGAGAGCTTC[A/G]GCAGCCTGGAACCCA | 9886 |
rs368704954 | snp | C/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002677 | CTATTGACAGAAGAA[C/G]GAACGAAACGAGCTG | 9886 |
rs368731790 | snp | A/C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988258 | CAACTTTTAACACAC[A/C/G]GTTATATTTATTTAT | 9886 |
rs368740760 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880627 | TTCCAGCACAACCTC[A/G]ACAACAAATAGAACT | 9886 |
rs368764044 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000310 | AGAGACTAAGGCTAG[C/T]GGCCCAAGAAGCAGA | 9886 |
rs368804238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957183 | ATACAAACAGGAGTA[C/T]GTTCTAAAATAATGA | 9886 |
rs368878306 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894684 | CACAAAATAAAGCCA[C/T]CATGAATTTTGGTAC | 9886 |
rs368895323 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965057 | AGAGTGAGTTACTTA[C/T]AAGGCATCTATTTGT | 9886 |
rs368979718 | in-del | -/TGTGTGTGTGT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880203 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGT]AGAGAGAGAGAGAGA | 9886 |
rs369018737 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920813 | GCATGTGCCACCATG[C/T]CCGGCTAATTTTTTG | 9886 |
rs369031876 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928639 | AAAGGGTAGTGGAAA[A/G]GGGAGTAGAAAGGGG | 9886 |
rs369069093 | snp | A/G/T | 3.32614e-05 | 0.00407797 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911365 | CCTCCTGGCACACGC[A/G/T]GTACTGGTCAATCGC | 9886 |
rs369070881 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870837 | GGCACATATAACCAT[A/G]TAATTACCAGCACTT | 9886 |
rs369080486 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960506 | TTGTACCAAATAAAT[G/T]ACTGTTTTGTCTGAA | 9886 |
rs369105064 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899719 | TAGACATTGGGGATA[C/G]AGTGATTAGTAAAAG | 9886 |
rs369114041 | snp | A/C | 0.000329739 | 0.0128359 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892875 | GAGATCAAGCTGGCA[A/C]CCAACAAGGATAACG | 9886 |
rs369199341 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926471 | ATACACATAGATGCA[A/C]AATTCCTCAATATAA | 9886 |
rs369218069 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956110 | TAGATGGCATAGCCT[A/G]CTACACACCTAGGCT | 9886 |
rs369218859 | snp | A/G/T | 0.000181319 | 0.00951998 | stop-gained, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911522 | AACGTTGGGTCTTTC[A/G/T]TAGTCCATGTCAGCG | 9886 |
rs369265671 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880246 | GAGAGAGAGACAGAG[A/T]GAGAGAGAGTGAGAG | 9886 |
rs369287909 | snp | C/T | 6.81419e-05 | 0.00583664 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60871630 | GGGGGCCAGCGGTGC[C/T]GCTCGAAGTATTCCT | 9886 |
rs369291867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917139 | TGCTACTAAGTTTTG[A/C]CGTTTGTTACAGCAG | 9886 |
rs369383415 | in-del | -/GTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947598 | TTTTTTTGTTTGTTT[-/GTTT]TTTTACTAAGCTTAA | 9886 |
rs369393750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976346 | ATTCTTTTCTATTTT[C/T]ATCACAGAGAGTAAG | 9886 |
rs369423919 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937549 | AGCTACTTAGGAACA[C/G]TGTCTGGAAGAAAAT | 9886 |
rs369424412 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904198 | GTGATCCACCTGCCT[C/T]AGCCTCCCAGAGTGC | 9886 |
rs369435497 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976459 | AAGTGTATCTAACTC[C/T]GAGTTAAGAAACTGT | 9886 |
rs369450641 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985761 | AGTCATGCCATCTTT[A/T]CACAAGATGCTTTTC | 9886 |
rs369493090 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961171 | ATGTTCAAGAGGCAC[G/T]GTGGCATGCCATGCA | 9886 |
rs369520359 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900030 | GAGCAAAGGCCCGAG[A/G]TAGGAGCCTGCCTGT | 9886 |
rs369590197 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983077 | TCTCAGTGTTCTTGA[A/C]TCTGTCTGATTTAAT | 9886 |
rs369592201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984912 | TACATCCAATCTATA[C/T]GCTAATAACAAAATG | 9886 |
rs369597564 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917980 | AAAACAAATGTACAC[A/G]CATCCATACACACAT | 9886 |
rs369601126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999852 | TCACCCAACCGTAAG[A/G]TAAATGCCATTTCAT | 9886 |
rs369609309 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927644 | AATAAATGATGCTGG[A/G]AAAACTGGCTATCCA | 9886 |
rs369609310 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983047 | AAAAAAAATTACAAG[A/T]GCTAGATGGTCTATT | 9886 |
rs369617981 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945484 | AGGATGCGTGAAAAA[A/T]TTCTAAAAGCAAACA | 9886 |
rs369646065 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998454 | AAGAAGACAAAAACA[A/C]CAGTCATATTAAACA | 9886 |
rs369662146 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898973 | ATTACGTTTGCACCA[A/C]CCTAATACTTGAGTC | 9886 |
rs369677700 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955827 | TATCACTATCTTGAA[A/C]ACTAAGGATGTGCTA | 9886 |
rs369702338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995632 | ATCAGAGTAAATTAT[C/T]TGAATTATCCATAAT | 9886 |
rs369733782 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902687 | CGTTTGCTAATTCAC[A/T]AAGGAGAGGCTAAGC | 9886 |
rs369736924 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875188 | ATTAAATCCAGAAGC[C/T]GCTCTGATGTGTGGT | 9886 |
rs369846150 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986885 | CCTTTCTGTGCCTCT[C/G]TAACAAAGACACAAG | 9886 |
rs369882550 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922194 | TCACTACTTCGCTGG[A/T]AAAGAAAGGAAAAAA | 9886 |
rs369886188 | snp | A/G/T | 0.000247177 | 0.0111146 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871532 | ACTTTCGTCTTGAGC[A/G/T]ATGCTTATTTAGTGC | 9886 |
rs369888003 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918193 | TTTCTTGACTACCCC[G/T]CTGGTCCAAAGGTCC | 9886 |
rs369901720 | in-del | -/TT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896158 | GATATTAAATAACTT[-/TT]AATCAAAACATTCAT | 9886 |
rs369905548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952126 | AGTTAGTTATAATTT[C/G]TTTTAATCACTCATA | 9886 |
rs369916439 | in-del | -/CCAAGTCTTT | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003350 | ACATTTGGGTTGGTT[-/CCAAGTCTTT]GCTATTGTGAATAGT | 9886 |
rs369927008 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871174 | AACATGAAAGCTGAA[G/T]TTTTTTTCTTTGTAT | 9886 |
rs369929246 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935859 | TATAATGGTGTGACA[C/G]TGCATCATCTCTTTC | 9886 |
rs369963363 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896687 | CTTGCCCTTGCCCAC[A/G]GAATGTTTATATCTT | 9886 |
rs370006154 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910147 | TTATAATTAAGTGGT[-/A]AAAAAAAAAGTCTCC | 9886 |
rs370014591 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002963 | ACTTTAAATTCTAGG[A/G]TACATGTGCACAACC | 9886 |
rs370028033 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890205 | TGTGAATTCTCTTTC[A/G]AATCTTTGCCTTCTT | 9886 |
rs370031783 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997328 | ACCAAAGATATTTGT[C/G]AAAATGCAGTTGTGT | 9886 |
rs370037858 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991529 | TCTGCCTCCTGGGTT[C/T]AAGCAATTCTCCTGC | 9886 |
rs370069661 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925032 | TGGTGATAAGTGAAC[A/T]CTTGCTCTCAGTTCA | 9886 |
rs370110646 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955867 | ATGAAGTATTTTTCA[C/T]TTAAATATTTTGTTA | 9886 |
rs370159564 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888934 | GAAGGACACTCTGGA[A/G]TTTTGATGACCGGTG | 9886 |
rs370168844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912012 | TCGCTCATTAGCCAA[C/T]ATCTGTTGTTGAAAA | 9886 |
rs370205291 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958711 | GAAGAGGTGATCCTC[C/T]TACCTGAGTCTCCTG | 9886 |
rs370219689 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996007 | TCATTTTATTCTCAC[A/C]ACAACCCCATTAGTA | 9886 |
rs370233725 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998228 | TCAATGATGCTTCAT[C/T]TAGGCTTTCCCAAGG | 9886 |
rs370277939 | in-del | -/CTTC | 0.00161258 | 0.0283494 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948953 | GTGGTTTAGTGGCAG[-/CTTC]CTTGAACAAATCATT | 9886 |
rs370294716 | snp | C/T | 1.74854e-05 | 0.00295676 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910846 | GTTTTGAAAAGGAAA[C/T]TGCATTCAAGCTCAA | 9886 |
rs370320153 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930826 | TCATCCCTTCTTACA[A/G]GGCTAGCCATCATTC | 9886 |
rs370336190 | in-del | -/GACTATGGTG | 0.00914312 | 0.0669923 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885120 | ATTGCACAGTATGGT[-/GACTATGGTG]GACAATAATGTATCG | 9886 |
rs370337112 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962477 | AAGTATTTATAAAGT[C/T]CAAATTGGATCTTAT | 9886 |
rs370344406 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996616 | TGGAATGTGCCATGG[C/G]GGCATTTTTCTCAGG | 9886 |
rs370366396 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914580 | TAATAATGCAGAATT[A/T]GTTTTCTGGTAGGCT | 9886 |
rs370386526 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894464 | ATATATAAATGAAAA[G/T]GAAACATGTCTTGTC | 9886 |
rs370402965 | in-del | -/ATCTCCATTTAGCTGTTCACAGACAGT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919132 | GACCTTTGTAGTCTT[-/ATCTCCATTTAGCTGTTCACAGACAGT]CTGAATGATGCTATT | 9886 |
rs370418509 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943037 | CGACTCTTCTGGTCT[C/T]AACTTCCTAGATTTT | 9886 |
rs370454260 | snp | A/T | 1.66189e-05 | 0.00288256 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886084 | TACATTCATAAAGAC[A/T]CCACTATGCTTTTAG | 9886 |
rs370504235 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910760 | TTTTCCTTTTCTTAG[A/G]CACAGTGCAGAACCC | 9886 |
rs370519361 | snp | C/T | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872250 | TAGTTGGTGCAGATG[C/T]GGTGCAAACACCAGG | 9886 |
rs370523055 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947527 | CTCTAGAGTTTTTTT[-/T]ATTGTGAGACTGTTA | 9886 |
rs370568274 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905574 | TCTGAGGCAGAAGGG[-/A]AAAAAAAAACCAAAA | 9886 |
rs370576709 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990040 | TAGGCTGGAGTGCAG[G/T]GGCGCGATCTCGGCT | 9886 |
rs370628911 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939069 | TGTCTATGCAATAAG[A/T]AAACTCAGGTGCAGA | 9886 |
rs370670323 | in-del | -/TCTG/TCTGTGTGTGTG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880177 | ATACTGAGGGATGAC[-/TCTG/TCTGTGTGTGTG]TGTGTGTGTGTGTGT | 9886 |
rs370725833 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943817 | GAGGCCCCCCTAGCG[A/G]CTCGGTCCCACAACT | 9886 |
rs370742775 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870893 | ATTCTTGGAGTTGAC[C/T]TTGTAATTACACCGA | 9886 |
rs370757581 | snp | C/T | 1.65778e-05 | 0.002879 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888734 | TCTGCTTCTCTTTCT[C/T]ACAGGCTCCTTCACT | 9886 |
rs370790191 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961870 | CTGGAGTGTAATGGG[A/G]TGATCTTGGCTCACT | 9886 |
rs370807287 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992809 | CTAACACAAAGGGGA[A/C]AAAAACACATTCCAT | 9886 |
rs370808677 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895684 | GCTGGGATTACAGGC[A/G]CAAGCCACCGCGCCC | 9886 |
rs370811486 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955336 | ATGAACCACCACACC[C/T]AGCCAGCAAGGGGAA | 9886 |
rs370834396 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916314 | GAGGCAGCCCTGCCA[A/T]TGGCTGTCACCAAGT | 9886 |
rs370855032 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988077 | GCTGGGACTACAGGC[A/G]CCCACCACCACGCCC | 9886 |
rs370863181 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002495 | ATCATTGGAAATAAG[A/G]TTAGAAAATTATCTG | 9886 |
rs370871250 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955214 | CACTTCCAGCTAATT[G/T]TTGTATTTTTAGTAG | 9886 |
rs370888479 | snp | A/C/G | 1.70851e-05 | 0.00292271 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893014 | AAAGGAAATCATAAA[A/C/G]GAAGCTTGTATTGCC | 9886 |
rs370892681 | snp | A/C/T | 0.00082149 | 0.0202513 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871685 | AGACCATAAGACCTG[A/C/T]GGTTCATTGATGCCT | 9886 |
rs370893421 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919500 | AATAGACCCAGAGCC[C/G]GGAAAGAGATGCAAG | 9886 |
rs370897719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994243 | TCTGACCTCAGGGTA[C/T]TTCTAGTCCAGTAAG | 9886 |
rs370898003 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955035 | GGAATCTTTTCTTTT[C/T]TTTCTTTCTTTTTTT | 9886 |
rs370909540 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944856 | GCGGGAGGGGTCCCC[C/T]CAGGGGGCGTAGGGA | 9886 |
rs370963506 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933459 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9886 |
rs370983264 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966928 | ATATAGCAGCACTGC[A/G]CCAGGCACTGGGGAT | 9886 |
rs371010476 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919497 | AAGAATAGACCCAGA[A/G]CCGGGAAAGAGATGC | 9886 |
rs371070052 | in-del | -/AAGA | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870255 | AAACTCAGAATGAGA[-/AAGA]GTCAGAACGAACTCA | 9886 |
rs371101089 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916731 | ACGTCCACGGAATCC[A/G]CGGAACTTGTGAATA | 9886 |
rs371118509 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897278 | GCTCAACTTTTTTTC[C/T]AATCTGAAATACCAG | 9886 |
rs371119447 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956970 | AAAAACCAACATATC[A/G]CTGTCTTGAACACTA | 9886 |
rs371126399 | snp | C/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883492 | CTGCGTTCCTGACCT[C/G]GATCAACTTCTCCCT | 9886 |
rs371172870 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940044 | CTTGGCCTGTAATGG[A/G]ATCTTCCCAATAATA | 9886 |
rs371176777 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926463 | TATATCTAATACACA[C/T]AGATGCAAAATTCCT | 9886 |
rs371212823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933613 | TAGTCCAAGCTAGTC[A/G]GGAGGCTGAGGCAGG | 9886 |
rs371235232 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908611 | CAGAGCCGGGAAATG[C/T]ACTGGTTAGGGACCT | 9886 |
rs371256415 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903509 | CACCAGTTCCAGAAC[A/G]AACCAGCTACAAAAG | 9886 |
rs371277757 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888247 | AGACACTCTTTTATC[C/G]GATTGGCTTTCCTTA | 9886 |
rs371315529 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994509 | TCCAGAAAATACAAA[C/T]GGTAGATCTCCAAGT | 9886 |
rs371340217 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887542 | CATGCTTAACAATTA[C/T]GAAAGGGTGCTGCGG | 9886 |
rs371368416 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989309 | TTGCACTTGTTTTAA[G/T]ACATCAGATTACAAA | 9886 |
rs371419749 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936978 | CATCCATCTTGCAAT[A/G]TGCATTTACCAAATA | 9886 |
rs371432442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879929 | GGCATGACTGCTTCC[A/G]TTCTGAACATGTACA | 9886 |
rs371449804 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990505 | TAGCAATTTCTCTTT[A/T]TTTTAATTCAAAAAT | 9886 |
rs371462959 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957620 | CAAATGCTAAAATGA[C/T]ATTGAAAGTGCTAAA | 9886 |
rs371463515 | in-del | -/GAAGTCTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931008 | CAATATTGAAGTCTT[-/GAAGTCTT]CCCTCTGCAACAACA | 9886 |
rs371467053 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911452 | ACGCCCTGGCACAGA[C/T]CAAGCGCGTCTTCCC | 9886 |
rs371520845 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946594 | GCACCTGGGGTTGTC[C/T]GTGCCAAAGTCTTAT | 9886 |
rs371578834 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930184 | TCTTTAAGAAAAAAA[A/G]TGAAAACAACCTATG | 9886 |
rs371634988 | snp | A/C | 1.66763e-05 | 0.00288753 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886065 | ATAAATACACAGGCA[A/C]ACATACATTCATAAA | 9886 |
rs371635417 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913051 | ATAATTGGGACTCAA[A/G]TGTTTGTTTAATTCA | 9886 |
rs371683443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896279 | AGCATTTCTATTTCT[A/C]TGGCTCTGTTACATT | 9886 |
rs371723108 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993875 | AATTCTTTTGTAGTA[A/C]TTAATTTTTTGGTGA | 9886 |
rs371756078 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884782 | TGTGGAATCTAAAAA[C/T]GTTGAACTCCAAAGT | 9886 |
rs371788077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965547 | ATATTTGTAAGAGAA[C/T]TAATTGGTGTGCCTT | 9886 |
rs371792290 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980532 | GTCCTTTGCTTATTG[A/C]GAGTTTTAAGTTGGG | 9886 |
rs371813495 | snp | A/G | 1.68286e-05 | 0.0029007 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910866 | TTCAAGCTCAACCAC[A/G]CTGTACTAGTCTTGG | 9886 |
rs371817204 | snp | A/G | 0.00016524 | 0.00908806 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872318 | GAGCAAAAGGAGGGT[A/G]AGACTATTTTCTAAA | 9886 |
rs371869131 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906951 | GGGAGGGACCCAGTG[A/G]GAGGTAACTGAATCT | 9886 |
rs371885548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982869 | GTGAATTTCATGTGC[A/G]TTTCATTTGCCCTCT | 9886 |
rs371889972 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904293 | TATAATGGAAATATA[C/T]CAAATTTGCATATTT | 9886 |
rs371911141 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991501 | AGTGGTGCAATCCTG[G/T]CTCACTGCAACCTCT | 9886 |
rs371941465 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921603 | TCATCTTTAAATCCT[C/T]AAATCTTGTCACAGT | 9886 |
rs371963067 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955816 | AAAAACCAACATATC[A/G]CTATCTTGAAAACTA | 9886 |
rs371966567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886953 | CCCAAAATAACAACA[A/G]TCTCCTAAATAACCA | 9886 |
rs371986397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982969 | GGCACAGAACTTTTA[A/T]TGTTCCATGGTCTTT | 9886 |
rs371992615 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919752 | ACTTTTTACTACATC[C/T]GCTCATGATTCTCAC | 9886 |
rs371996872 | snp | A/C | 4.96389e-05 | 0.00498166 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892841 | TGGCTCGATTAACAG[A/C]TTCCAGGTCGGCATA | 9886 |
rs372021030 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897494 | TCTTACCTGGTTAAG[G/T]GAAAGAATAATTCTG | 9886 |
rs372046288 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880890 | TTACAGGTATCCATA[C/T]AAATTTGTTTCTGTG | 9886 |
rs372051144 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955377 | GGTTTTAAAATGCCA[A/C]AATTCAATTCATGTG | 9886 |
rs372087538 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889128 | GTATGGTAAGCCAAG[C/T]TCCTTTGCTACCTCT | 9886 |
rs372180261 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945919 | GGCGGGTGGCTCACG[C/T]CTGTAATCCTAGCGC | 9886 |
rs372203681 | snp | C/T | 0.000170619 | 0.00923475 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911314 | CAACCAGCAATGATG[C/T]GCCCTAGGGATGCTG | 9886 |
rs372237954 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906973 | ACTGAATCTTGAGAG[C/T]AGGTCTTTCTCATGC | 9886 |
rs372255126 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952073 | AGCCCCCCACCCCCC[A/C/T]AAAAAAGAACGGTAC | 9886 |
rs372257928 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947996 | TCATTGTTTACAAAG[C/T]TTCACTTGTTATAAT | 9886 |
rs372346886 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929348 | TTCTTGAAAGAAAAA[C/G]GACATAATAATACAT | 9886 |
rs372362272 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900654 | TTAAAAGGCCTTATG[G/T]ATATCAGAAAGTAAA | 9886 |
rs372373042 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934885 | CTTCATTGCTTATGT[C/T]TTAAAAGTACATTCA | 9886 |
rs372374351 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927069 | GTAGCATTGCTATAT[A/G]CCAACAATGAACAAT | 9886 |
rs372395232 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997489 | ACTTTAGCAAGGATT[C/G]CTGTCTATGTTAGAG | 9886 |
rs372402462 | snp | C/T | 0.000691882 | 0.0185866 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871537 | CGTCTTGAGCGATGC[C/T]TATTTAGTGCAATAT | 9886 |
rs372430478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999163 | GGTTAAGTTACTTGG[A/C]TAAAGGAGGAGTGGC | 9886 |
rs372444556 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875197 | AGAAGCTGCTCTGAT[A/G]TGTGGTCTTTCACTA | 9886 |
rs372490577 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964861 | GTGGATTAAACTTCA[A/C]CCTTCTTTATAAAAA | 9886 |
rs372499949 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932535 | AAAAAAAAAAAAAGA[A/C]AGAAACAAGAAACCC | 9886 |
rs372542434 | snp | C/T | | | nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60985868 | GGGGGAAAATAAACT[C/T]CAATTCCATTTTCAT | 9886 |
rs372620263 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988737 | TGATTCCATGTCTTT[A/G]CTATTGTGAATAGTG | 9886 |
rs372623942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959441 | TCACTTTAAAAGCTA[C/T]GTGGACAAGAAAGGA | 9886 |
rs372689953 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960922 | TCATTGTCAAACTCT[C/T]CCCTTCTAAAGCTCT | 9886 |
rs372720503 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878789 | ATGCATGCTGGAGTT[C/T]GCCAGAGAGCCAGGC | 9886 |
rs372751302 | snp | A/G | 1.65913e-05 | 0.00288017 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872334 | AGACTATTTTCTAAA[A/G]AGGGGCTACAAAGAA | 9886 |
rs372766160 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990531 | AAAATAATTCTCTCC[G/T]GACCAGTATTCTCCA | 9886 |
rs372783546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892092 | TAAACTGTGAGTCAA[C/T]TAAACCTCTTTCCTT | 9886 |
rs372796194 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943262 | TTTGATACTGCTGGG[G/T]ATGGAAACGGTGCAG | 9886 |
rs372833321 | snp | A/G | 5.16409e-05 | 0.00508112 | synonymous-codon, nc-transcript-variant, missense | RHOBTB1 | GRCh38.p7 | 10:60871635 | CCAGCGGTGCCGCTC[A/G]AAGTATTCCTGGTTG | 9886 |
rs372848856 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961588 | GAGAACCAGCTTAAC[A/C]ATTTTCAAACTATGT | 9886 |
rs372863297 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946483 | GTAATCCCCACAACA[A/G]CTGATGAGGCAGATG | 9886 |
rs372885647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999568 | GATAGCTGGTGTTAA[A/G]GATGCTTCAAAACCA | 9886 |
rs372895485 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873197 | CTTGCTGTTAGATTT[C/T]TCTCTGAAAACAAGG | 9886 |
rs372930716 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923340 | AAGAAGATAATGTAC[A/G]TTTATAAACTAATAG | 9886 |
rs372958833 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962724 | TGGAAAAAACTGCTG[A/G]CCCAGTCAATTTTGG | 9886 |
rs372972105 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927010 | AACTATCAGAACTGA[C/T]AAATAGTAAAGTTTC | 9886 |
rs372998480 | snp | C/T | 0.000363258 | 0.0134721 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888812 | TGGAAGAAGAGGTAG[C/T]GAGGTAAATTCGATG | 9886 |
rs373050300 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989196 | AGAGCAAATGAGAGA[A/G]AAAAAAAGTAGAAGT | 9886 |
rs373074757 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996998 | ATTTTTGTGGTCCAA[C/T]AGAAACATTTTTGAA | 9886 |
rs373081088 | in-del | -/TA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903841 | TTTTTTAAGTTCACA[-/TA]GTGATTTACGTTTTC | 9886 |
rs373107461 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909740 | AAACTATCTATGATG[A/T]AGGATACTAAGTTCA | 9886 |
rs373119390 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953169 | TTTAAATATATGGAC[A/T]ACATGGGTAAGGTTA | 9886 |
rs373132754 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883218 | TGAGCTGGTCTGAAT[A/G]TATACAAACCTATTA | 9886 |
rs373140849 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945953 | GGGAGGCCGAGGCGC[A/G]CGGATCACGAGGTCA | 9886 |
rs373152383 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990618 | CTACTTTCCTAGAAC[C/G/T]CTTGCTCCTCTGCCC | 9886 |
rs373191317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923485 | TGTAAAATTAATTAG[C/T]GAGGTACAGGTCAAG | 9886 |
rs373201230 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942960 | AATCTCAAGCTGAGC[A/G]TCTGGCTGGAGTTCA | 9886 |
rs373213553 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955834 | ATCTTGAAAACTAAG[A/G]ATGTGCTATCACGAT | 9886 |
rs373280011 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977642 | AATACATCTTTTCTG[A/T]CCCAATCCCCAGATG | 9886 |
rs373288065 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991800 | GTAGCATGCCTTCTG[C/T]GTGTATGCCCGGTCT | 9886 |
rs373327946 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983672 | CTAATACACCTAAAC[A/C]CTGAAATAGGTGAGC | 9886 |
rs373352785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973454 | ACAGCCTTCTTTTTT[A/G]TTGTTGTTTTTAATT | 9886 |
rs373355305 | in-del | -/AT | 0.452597 | 0.146474 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986405 | AAATATAAATAAAAG[-/AT]ATATATATATATATA | 9886 |
rs373407479 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879766 | ATATATTTTGTATGA[C/T]TGCACCTCTCTCTCC | 9886 |
rs373429694 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973581 | TCATATTCAAAAGAA[A/G]CAACACCAACAACTG | 9886 |
rs373467900 | in-del | -/ACTATGAGCCACTGAGGCAG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903695 | GGGCCCCTGGGTCAG[-/ACTATGAGCCACTGAGGCAG]GGGGGGTTCTATCTC | 9886 |
rs373550319 | in-del | -/TG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872966 | CCCTCACTTTCTGTC[-/TG]TGCCCTTCTCTGACT | 9886 |
rs373589684 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994788 | GTACCTTAAACCAAT[C/T]TTGTATTGTTCCATC | 9886 |
rs373611958 | in-del | -/A | 8.28555e-05 | 0.00643591 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875049 | CATGCTGTTCTGGGG[-/A]AGAGAGAGGGGGCAG | 9886 |
rs373672834 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981232 | AATGAGAAGAGAAGG[C/T]TATAATTAGAACTCC | 9886 |
rs373712081 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950466 | CTCTTTATGAAACAA[A/G]TTTAAAAAACCAAAA | 9886 |
rs373818552 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000572 | CACCTGCTGGACTCA[C/T]TATTTGAGTGACATC | 9886 |
rs373839596 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961638 | TCCTCTCAAATTCTT[-/A]AGAGATGGGGGGACT | 9886 |
rs373860174 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993825 | AAAGGCAACATGTAA[C/T]TGATTACTGTAAAAA | 9886 |
rs373874267 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002748 | TGGTTTTGTCTTGGA[A/G]TTTATGCAAATGGTT | 9886 |
rs373904843 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872283 | GCCAACTGGTGGGCA[C/T]TGTGAAACTGCAGAA | 9886 |
rs373926518 | in-del | -/TTG | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947183 | AGTTTATCTCTGCTC[-/TTG]TTATTTCCATGAAAA | 9886 |
rs373991144 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914463 | TCTTTTAAGGGTGAA[-/T]TTTTTTTTATTTATT | 9886 |
rs373993140 | snp | G/T | 3.31e-05 | 0.00406803 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875057 | TCTGGGGAAGAGAGA[G/T]GGGGCAGGAGAACAT | 9886 |
rs374030537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875241 | TGCCAGCCACTTCAC[C/T]CACACCTCTGGGGAC | 9886 |
rs374059598 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913162 | TCTTTTTCACAGTTA[C/G]GACTATTGGAACATG | 9886 |
rs374062496 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878131 | TTCAGGCTATGCTGC[C/T]TATAAATATCCTGTG | 9886 |
rs374066494 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904686 | TCAGAGTCTTCTAGG[C/T]ACTGGCTAAAATTGG | 9886 |
rs374129849 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981126 | ATTTTTTTGAAATGA[-/G]GTCTAAGATTTTTGT | 9886 |
rs374188749 | snp | C/G/T | 6.95698e-05 | 0.00589753 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871701 | GGTTCATTGATGCCT[C/G/T]TTATGTGCTAGGCCT | 9886 |
rs374289512 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884354 | AGACAAGTAAAACAA[A/G]CCTCTTAGGACAATA | 9886 |
rs374290142 | snp | C/G | 4.96454e-05 | 0.00498199 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875058 | CTGGGGAAGAGAGAG[C/G]GGGCAGGAGAACATT | 9886 |
rs374303226 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945623 | CTTCCTCACTTGCTT[A/G]TATTCTCTTGAAGTC | 9886 |
rs374303549 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924178 | CCCATTGTATCTTAT[C/T]AAAATGTCTTCCAAA | 9886 |
rs374319395 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955039 | TCTTTTCTTTTCTTT[C/T]TTTCTTTTTTTTTTT | 9886 |
rs374343927 | snp | C/T | 3.30196e-05 | 0.00406309 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888276 | TACGTGAAAGGCTTT[C/T]GTAATCTCCTGGTTC | 9886 |
rs374356419 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891853 | TCCCATAATCCCCAT[G/T]TGTCACGGGAGGGAC | 9886 |
rs374358384 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918189 | AGCCTTTCTTGACTA[A/C]CCCTCTGGTCCAAAG | 9886 |
rs374397850 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976643 | TTGTCCAACAGACCC[A/G]ATAGGAAATCACACA | 9886 |
rs374413434 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944276 | GCAGCCAGGCGGAAC[C/G]GAGCACCCGGCACCT | 9886 |
rs374460650 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960006 | TAATAATAAACAGTA[C/G]GCTGGAAATACTAAT | 9886 |
rs374461338 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880264 | GAGAGAGTGAGAGAC[-/AG]AGAGAGAGAGAGAGA | 9886 |
rs374467534 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942914 | GTACACCACCGCAGC[G/T]GTTGGGGGTGGGGGA | 9886 |
rs374472333 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962176 | AGTGGAAATTTTCAT[A/G]ATGAGCCACAAATTA | 9886 |
rs374487194 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875329 | GATGATAACTCCTGG[C/T]CACACGAGACTATTT | 9886 |
rs374490526 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955873 | TATTTTTCATTTAAA[C/T]ATTTTGTTACATTTA | 9886 |
rs374497246 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940223 | GAGTGGGGGTTATCA[A/G]CACATTAAAAAAGAT | 9886 |
rs374501505 | snp | C/T | 5.24462e-05 | 0.00512058 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888200 | AATGGCTCTGCCCCG[C/T]GGCCCACTCACCCGA | 9886 |
rs374588295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919735 | GCTGATATGAAAGAA[A/G]CACTTTTTACTACAT | 9886 |
rs374590916 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914380 | GAAACACAGGTTCTA[A/G]TTGGAGTCTCCCAAC | 9886 |
rs374622216 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892021 | CATACGAAGAAGGAT[A/G]TGTTTTCTTCCCCTC | 9886 |
rs374635367 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891408 | TGAAGTGGTGCAATC[A/G]TGGCCCACTGCAGCC | 9886 |
rs374639064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875540 | GAGTCCTCTAGACTT[C/T]AGACACGTTCCTGTT | 9886 |
rs374649518 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994674 | TAAATTCATTCAATA[A/T]ATATTTGAGTCTACT | 9886 |
rs374686856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925329 | AATATGCTCCTGAAT[A/G]AATGTTGAGTCATTG | 9886 |
rs374719618 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869345 | ATGCACAAGCCCCCA[G/T]GACCCAGCACCCTTA | 9886 |
rs374749965 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908863 | AACATGCACACAAAG[C/T]AAGGCCCTAAGGAGA | 9886 |
rs374757425 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898578 | ATGGAGGATGGAGAG[A/G]CCTGTAGGGGAGCGC | 9886 |
rs374771775 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965563 | TAATTGGTGTGCCTT[C/T]TGTGAGTAATGTGCT | 9886 |
rs374792663 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974133 | TTTACCTGTGCATCA[C/G]TAAGTCTATAATCAG | 9886 |
rs374806622 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939152 | AAAACTTGCTAATTC[A/G]TTCTTTAGTGGATAA | 9886 |
rs374818642 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955730 | GTCAGTTACAGATAC[G/T]CAGAAGGGTCCAGAG | 9886 |
rs374825196 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913040 | AAGCCTAATACATAA[C/T]TGGGACTCAAGTGTT | 9886 |
rs374835836 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955393 | AATTCAATTCATGTG[C/T]TAACTGAACACACTT | 9886 |
rs374841085 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878355 | TGACATTAGGGGCCC[G/T]CATGCCAAGCACCTT | 9886 |
rs374863938 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972603 | GACAGGTTGATGGGT[A/G]CAGCAAACCACCATG | 9886 |
rs374879481 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888977 | GAGGTAGGAAGGGTG[C/T]CTGAAGTAAAGGTTT | 9886 |
rs374888652 | snp | A/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002942 | TCTTCTTATTATTAT[A/T]ATAATACTTTAAATT | 9886 |
rs374897782 | in-del | -/GTGT/GTGTGT | 0.0912534 | 0.193131 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001043 | CCCCCGCCTCCGCCA[-/GTGT/GTGTGT]GTGTGTGTGTGTGTG | 9886 |
rs374936128 | snp | A/G | 8.23988e-05 | 0.00641815 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871549 | TGCTTATTTAGTGCA[A/G]TATCTTCCTTCTCTC | 9886 |
rs374949792 | in-del | -/AT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985581 | GTGGATAGAAGAGTT[-/AT]GTTATTTTAGTAATC | 9886 |
rs375055635 | in-del | -/GAGA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924526 | AAAGAGAGAGAGAGA[-/GAGA]CCCTGATATAGTAAG | 9886 |
rs375068836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872552 | GCTTAAAGTATGCCT[C/T]GCCCTCCCGCCCTCC | 9886 |
rs375083594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932678 | AGATGGCAAAGATGT[G/T]CATGATACATCTTTA | 9886 |
rs375131281 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942818 | TTACTATCTGCTGCT[C/G]GTCAGAGGACTTATA | 9886 |
rs375143684 | in-del | -/GGAACCTTCTTTATGG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955348 | ACCCAGCCAGCAAGG[-/GGAACCTTCTTTATGG]TTTTAAAATGCCACA | 9886 |
rs375150036 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959057 | GGTCAGGAATGCAAA[A/G]TTGCCTCAACGTTCA | 9886 |
rs375183313 | snp | C/T | 0.000545725 | 0.0165095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872322 | AAAAGGAGGGTAAGA[C/T]TATTTTCTAAAGAGG | 9886 |
rs375282864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931604 | AAAACTAATGGGTAT[A/G]TTAAGTATAACCCTT | 9886 |
rs375288467 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948555 | AGATTCATGCTGTCC[A/C]TCTCTCTGCTCTGGA | 9886 |
rs375303992 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955819 | AACCAACATATCACT[A/G]TCTTGAAAACTAAGG | 9886 |
rs375325793 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871509 | TGGAGATGAATTCCA[A/G]AAGCACCACTTTCGT | 9886 |
rs375368271 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940431 | AAAAAGTCTTGCTTA[A/C]TATTTGGTTGTTATC | 9886 |
rs375415480 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930324 | ATTGTTGTGAAGATT[A/G]TATTAGATAATGCTT | 9886 |
rs375437812 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895760 | GGTTAACCCTTGTTG[A/T]TCTAAATACAAATGC | 9886 |
rs375441324 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936652 | AGTGTGGTCCACAGA[A/G]CAGCAGCACTGGCAT | 9886 |
rs375477490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994297 | TGAAATAATCAAATG[C/G]TAGTATACTACAATA | 9886 |
rs375528564 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907080 | TCTTGCCTGCCACCA[C/T]GTAAGATGTGACTTT | 9886 |
rs375572903 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991373 | ACCTGATGACATCCC[C/T]AGACTTAAGCAGTTC | 9886 |
rs375615429 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881758 | GCTTAAAGAAGAAAT[A/C/G]GCAAAATGAACATCC | 9886 |
rs375629001 | snp | A/C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954101 | TTATTTATTTATTTG[A/C/G]CTCTACAAATACAAT | 9886 |
rs375642943 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938945 | GTTATCACAGCAGTC[A/G]TTAGGAGTTTGGTCT | 9886 |
rs375681933 | snp | A/T | 3.31433e-05 | 0.0040707 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872145 | AGCTTCCATGAGAGG[A/T]GAGGAGAGCTGGATG | 9886 |
rs375684282 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905721 | AGTTTCACTGTGCAA[C/T]GGGCTGCTTGCCATC | 9886 |
rs375713187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880164 | CCAGTCCCTCACAGA[A/T]ACTGAGGGATGACTG | 9886 |
rs375759880 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926220 | CCAGCCAGGGCAACA[A/G]AGCAACACTCTGTCC | 9886 |
rs375779508 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945944 | TAGCGCTTTGGGAGG[C/T]CGAGGCGCGCGGATC | 9886 |
rs375810290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911641 | GGGAGTTTTGCCTTC[A/G]TCCAGCCACTTCCTT | 9886 |
rs375846877 | snp | A/C | 3.32679e-05 | 0.00407834 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877917 | CCTTACCTGCAAGTG[A/C]AACCAAGTGTGGCAG | 9886 |
rs375848133 | snp | A/G | 4.94947e-05 | 0.00497443 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892859 | CCAGGTCGGCATAGC[A/G]GAGATCAAGCTGGCA | 9886 |
rs375856894 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990229 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 9886 |
rs375860429 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998863 | AACTCTTCTTAGAGA[C/T]TGCAACGCAGCAGGA | 9886 |
rs375873349 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905246 | ACAAGGTCAGCAGTT[C/T]GAGACCACCCTGGCC | 9886 |
rs375885230 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891654 | TGCCCAGCCTAGAGG[A/G]GGGTATTAATATCAA | 9886 |
rs375887731 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896429 | TAAAAGAATCAAATA[C/G]GATTTAAATGGAGTC | 9886 |
rs375897944 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895357 | AGGTGCTATGAGAAT[C/T]TGTGCTCATTATTTT | 9886 |
rs375903386 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908709 | TCAATGTGATATTAC[A/G]TATTTAGCATTTACA | 9886 |
rs375920989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928588 | TGAGCTCATGGAAGT[A/G]GAGAATATAATAGAA | 9886 |
rs375927989 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990278 | GTCAGCCACCGTGCC[C/T]GGCCAACCTCAGACT | 9886 |
rs375960484 | snp | C/T | 1.92261e-05 | 0.00310044 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911334 | TAGGGATGCTGAAGA[C/T]ACTCTGTGCATCTTA | 9886 |
rs375965857 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886724 | AAGAGATGTGGGGGG[A/G]GGTGGGTCTGGCTAT | 9886 |
rs376003439 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932893 | TAGTAAGTTACTCAC[C/T]GAAAGCATTCTCTAA | 9886 |
rs376005127 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996969 | ACTCAACTCTTATTA[C/G]TACTTATCAATTTAT | 9886 |
rs376017888 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921752 | TCTCTGGTGACTGAT[C/T]ATTAAGCCCTGTGGC | 9886 |
rs376027429 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967558 | GAGAAAAAGAACAGA[A/G]CTGTAAGATTTTTTT | 9886 |
rs376056060 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878656 | TTATCAGTAGATTCG[C/G]AGAATCCAAAGGACT | 9886 |
rs376125571 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961863 | ACCCAGGCTGGAGTG[C/T]AATGGGATGATCTTG | 9886 |
rs376141093 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896334 | AAAATAATTGGGAGT[A/G]GTGAGTGTGATGAGG | 9886 |
rs376150249 | snp | C/T | 0.00319074 | 0.0398324 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970788 | TTTACAGTGCAAGAT[C/T]AATGCTATGGTTTTC | 9886 |
rs376186518 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936794 | GAGCACAGCTCTAAA[A/G]GCAATTAATTCCTTG | 9886 |
rs376190012 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923557 | TCTTTGTCTTTACTC[A/G]TGATTGACCAAAGAC | 9886 |
rs376229437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996817 | GTGTATTTGAAATCC[A/G]GATTTAACTAGGCAT | 9886 |
rs376242603 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913115 | GATTAAGGGCATTGA[C/G]AAGGATATATAGAAA | 9886 |
rs376286564 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983343 | TAACAATTAACTGAA[G/T]GAAATTTGCTTATTA | 9886 |
rs376295711 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990013 | TTTGAGATGGAGTCT[C/T]GTTCTGTCGCCTAGG | 9886 |
rs376349255 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963613 | CATGAGGTCATGTGT[A/T]CCATTGGAACAGGAA | 9886 |
rs376350761 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931820 | TGAGTATCAGACACA[G/T]AAATTGAACCATATA | 9886 |
rs376507792 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930672 | CATGGCTTACCTCAC[C/T]TATTATGCACCTTAC | 9886 |
rs376542498 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955030 | CAAGGGGAATCTTTT[C/T]TTTTCTTTCTTTCTT | 9886 |
rs376562891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949838 | GTGAAGACAAAGTAT[C/T]TTTTCCATTGCAGTT | 9886 |
rs376582036 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892943 | ACATGCTTTTCACAT[C/G]ATTTAGGGAATTGGG | 9886 |
rs376586327 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956898 | CTCAGAAGGGTCCAG[A/G]GTTTGAATGCAAGGG | 9886 |
rs376586969 | snp | C/T | 3.31126e-05 | 0.00406881 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888250 | CACTCTTTTATCCGA[C/T]TGGCTTTCCTTACGT | 9886 |
rs376601979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996716 | ACTAATGACACTGAA[C/T]ACTAATGTTCTCTGA | 9886 |
rs376614235 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910425 | AAATGACCTTCTAAT[-/A]AAAATAATAGACTTT | 9886 |
rs376668767 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955719 | GTCTACAATGTGTCA[G/T]TTACAGATACTCAGA | 9886 |
rs376790581 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945666 | GGTGCTCTCTAAATC[C/T]CCCAGAGACCCCAGA | 9886 |
rs376819942 | snp | A/G | 4.95479e-05 | 0.0049771 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874971 | GAGCCAATTCCAAGT[A/G]AGAGAGCACTTCTCC | 9886 |
rs376918236 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892614 | TTGACAAAAATGAGT[C/T]CTGACACCAGAGATG | 9886 |
rs376987050 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895871 | AGTTTAACCAAAAGG[C/T]TAAGCATTAGGAATC | 9886 |
rs377069196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998266 | AATATATTAGCCATT[C/G]ACACGTGTCTTTTAT | 9886 |
rs377081144 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915212 | ATTTTATCCTTCTCC[A/G]CTTGTTATAGGCTCT | 9886 |
rs377090607 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949349 | CTGTCCCAAATACCA[C/T]GGGCTGTCTTTGAAA | 9886 |
rs377099228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924967 | GGGCTTGGTGGCAAG[G/T]GTTTAGATGACGGGG | 9886 |
rs377161073 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984152 | CCAGTTAATATGCAC[A/G]TACCTTGAAAAGGGT | 9886 |
rs377182527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922626 | GAGTAATGAGAGCCA[C/T]ACTGACTTGGGACCA | 9886 |
rs377193518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948017 | TTGTTATAATAGTTG[G/T]GTAGAGACAACTCAT | 9886 |
rs377195519 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935760 | TAAGTACTCAAAATG[C/T]ATCATTTTCTGGTTA | 9886 |
rs377206200 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942922 | CCGCAGCGGTTGGGG[G/T]TGGGGGAGCCCCAAA | 9886 |
rs377207087 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981127 | TTTTTTTGAAATGAG[C/T]CTAAGATTTTTGTTT | 9886 |
rs377217989 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905221 | TTTGGGAAGCCAAGG[C/G/T]GGGCAGATCACAAGG | 9886 |
rs377220710 | snp | A/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882397 | CAACCCAGGCATGCA[A/T]TTTTAATGAACCACT | 9886 |
rs377228770 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955846 | AAGGATGTGCTATCA[C/T]GATTGATGAAGTATT | 9886 |
rs377260760 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982864 | CACATGTGAATTTCA[C/T]GTGCGTTTCATTTGC | 9886 |
rs377274271 | snp | A/G | 3.29685e-05 | 0.00405995 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872296 | CATTGTGAAACTGCA[A/G]AAAAGTGAGCAAAAG | 9886 |
rs377287180 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000196 | GGGGTTTAAATTGCC[A/C]ATACATGAAAACTTT | 9886 |
rs377300100 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989197 | GAGCAAATGAGAGAG[A/G]AAAAAAGTAGAAGTT | 9886 |
rs377301884 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927189 | GTTACCTACAATGAA[A/G]GCTATAAGACATTAA | 9886 |
rs377318779 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914442 | CCTCAGTGGTGGGAA[A/T]CCTTACTCTTTTAAG | 9886 |
rs377322874 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933630 | GAGGCTGAGGCAGGA[A/G]GCGGAGGTTGCAGTG | 9886 |
rs377326981 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950846 | CCCCCAATTCCTCCC[C/T]CCCCAAATGCTGACT | 9886 |
rs377332974 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979056 | TATATTTATGGCTTC[C/T]TTGTCATCAGTAGGT | 9886 |
rs377334453 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886766 | TGGATTTAAACTGCC[A/G]GGTTCCAGCAATCCT | 9886 |
rs377351846 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905557 | TAACAGTGCCATATT[A/G]TGTCTGAGGCAGAAG | 9886 |
rs377446404 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971530 | CATTCCTTACACCTT[A/G]TACAAAAATTACCTC | 9886 |
rs377462729 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918872 | CTGACTCAGCCTCCC[A/G]AGTAGCTGGGATTAT | 9886 |
rs377470699 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947010 | GTGATCAGAGAAAGA[C/T]GTTGCCACATGGTAC | 9886 |
rs377492214 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933491 | CTTTGGGAGGCTGAG[A/G]CAGGCAGATCACAAG | 9886 |
rs377537856 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991729 | AGCCACCGCACCCGA[A/C]CTTCCCTCAGTCTTT | 9886 |
rs377554492 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938626 | TAGTTCAAATTTAAA[C/T]ACAAAATTTACAAAG | 9886 |
rs377555430 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954630 | TGTCAGTGGTGTCGC[A/G]TATTCTTATTTGATA | 9886 |
rs377643031 | snp | A/G | 6.59522e-05 | 0.0057421 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911525 | GTTGGGTCTTTCGTA[A/G]TCCATGTCAGCGTCC | 9886 |
rs377703407 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895525 | TTCCCCTGATTCAGC[C/T]TCCTGAGTAGCTGGG | 9886 |
rs377748134 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873268 | GAGAACCAATTGTGT[A/G]CATTTCTTCCCTACT | 9886 |
rs386744483 | multinucleotide-polymorphism | CA/TG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903454 | TGACTGGGTACAAAA[CA/TG]GAGGTCACGTGCATG | 9886 |
rs386744484 | multinucleotide-polymorphism | AA/GC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933495 | GGGAGGCTGAGGCAG[AA/GC]AGATCACAAGGTCAG | 9886 |
rs386744485 | in-del | AAATTAGC/TACAG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951906 | TACTAAAAATACAAA[AAATTAGC/TACAG]CGGGCATGCTGGCAG | 9886 |
rs386744486 | in-del | AGG/GT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953069 | TACCTTGTGCCAGCA[AGG/GT]TCAGGTTGATGAGAT | 9886 |
rs386744487 | multinucleotide-polymorphism | CCA/TAG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955689 | AAGAAAGCCTTCCCT[CCA/TAG]TCTAAATTTGTGGTC | 9886 |
rs386744488 | multinucleotide-polymorphism | AG/CC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955806 | TTACAGCTTGAAAAA[AG/CC]AACATATCACTATCT | 9886 |
rs386744490 | multinucleotide-polymorphism | AT/CA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988496 | AGTGTCTGTTGTTCC[AT/CA]TCTTTATGTCCATGT | 9886 |
rs397693305 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942872 | TATTTTTTTTTTTTT[-/T]CTGTTTAGAGTATGT | 9886 |
rs397814740 | in-del | -/AAAA | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932532 | AAAAAAAAAAAAAAA[-/AAAA]GACAGAAACAAGAAA | 9886 |
rs398013722 | in-del | -/A | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893117 | AATTAAAAAAAAAAA[-/A]GACCAGATATTAAAA | 9886 |
rs398013723 | in-del | -/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896986 | AAAAAGCATTTTTTT[-/T]CAGTTATCTTTCGAG | 9886 |
rs398013724 | in-del | -/A | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928341 | AAAACAAAAAAAAAA[-/A]GAAAATCAGTATATC | 9886 |
rs398013725 | in-del | -/A | 0 | 0 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946191 | TCAGAAAAAAAAAAA[-/A]CAAAAAACTGACTTC | 9886 |
rs398013726 | in-del | -/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961826 | GTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCCC | 9886 |
rs398013727 | in-del | -/G | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985234 | TATGGGTGGACAAAG[-/G]AGAGTAAACTGTCCA | 9886 |
rs398097013 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887088 | TTTAAAAAAAAAAAA[-/A]CAGAATCCAATTGAG | 9886 |
rs398097014 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967247 | AATTAGAAAAAAAAA[-/A]TATAGCAGAATACAT | 9886 |
rs527250962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921158 | TCACCATGTTGGCCA[C/T]GCTGGTCTTGAACTC | 9886 |
rs527258561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970316 | GGTAGTCACAGCTTA[C/T]ATTCAGCATAACTAA | 9886 |
rs527285158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876631 | TGAAAAAAGTAATTG[C/T]CCATGGAAGCCTCCC | 9886 |
rs527298434 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937554 | CTTAGGAACAGTGTC[C/T]GGAAGAAAATGAGAG | 9886 |
rs527378291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985265 | TTTCAAATAATTCTA[C/T]GTTTTTTAGGCACAA | 9886 |
rs527415023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908752 | AGTGCAAGAGAGAGG[A/G]GCTCTGGTTTTTATT | 9886 |
rs527417486 | snp | A/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871591 | ACACGCTGGTAGTGA[A/T]CTTCTTCCTTCAGGT | 9886 |
rs527419881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998330 | ACCAACAACTATGTG[C/T]TATTCATCACTGTGC | 9886 |
rs527466234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983246 | AAGAAATGCTTCCTT[A/G]GGGCTATTCCAGTGA | 9886 |
rs527503691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975716 | GAACAAAATGGTTTT[C/T]CAGTTTTTCCATATA | 9886 |
rs527525697 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933710 | TCAAAAAAGAAAAAA[A/C]AAAGGAATGTTCATC | 9886 |
rs527547708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873559 | AGTGCAACAAACAGA[A/C]ACAACTGCAAATCAT | 9886 |
rs527588911 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942738 | GTTTGTAAACAAACT[C/T]ACCAGAGTATGTTTA | 9886 |
rs527605910 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972653 | ACAAACCTGTATGTT[C/T]TGCACATGTATCCCA | 9886 |
rs527610319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927962 | TAACCAGAATATATG[A/G]GCAGCTCAAACAACT | 9886 |
rs527631223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976438 | TCCAATGCCCACTCA[C/T]AGGTCAAGTGTATCT | 9886 |
rs527667734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977612 | ACTGTTAATATTGTA[A/G]ATTCTGTAAATCTCA | 9886 |
rs527668519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987652 | CAGGTTTCCGGGTGC[C/T]TCTAGTCTTTTTCTT | 9886 |
rs527688857 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877631 | CAAATGATTCAGCAT[A/G]CATACAGCGTGTGCC | 9886 |
rs527712459 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902082 | CAAGGCTGGGTCAGG[A/C]ATAGGAATCCCAGCT | 9886 |
rs527724553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936163 | TAGAGTTCTGACGTA[C/T]GTCTTTGATGTTTCA | 9886 |
rs527736749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971511 | AGAAAACTGAAACTG[G/T]ACCCATTCCTTACAC | 9886 |
rs527770514 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929519 | ATTAAATACTAAAAA[A/C]AAACAAACAAAAGGT | 9886 |
rs527791847 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931502 | ATCCATATTGTAGCA[A/C]CTTTCACTACTCCAT | 9886 |
rs527824590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885639 | GTTGAGGCACAGGAA[G/T]GCGGCTTCTCAAGGT | 9886 |
rs527862714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999013 | TCACCAGATTATTAC[A/G]AGAATTTAATGAGAT | 9886 |
rs527862757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991564 | GCCTCCTGAGCAGCT[A/G]GGATTACAAGCGCAT | 9886 |
rs527868143 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986118 | AGTTAGAGCAAAGAA[-/G]GCTGAAATGACTACT | 9886 |
rs527871012 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958514 | TGGATTTCCAAAACA[-/T]TTTTTTTCAGGAGAA | 9886 |
rs527874261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948842 | AAGAGGCTGGTGACA[C/T]ATTTATACTGCTCAT | 9886 |
rs527876548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955981 | TGGGCCTCATTTGTT[A/C]ATAGTCTGGTAATAC | 9886 |
rs527911499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949391 | TTCGTAGTTTTTGCA[C/T]TTGGGTAAAAGTGAA | 9886 |
rs527914231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903358 | AATAAGAATGGAGTC[C/T]CATGCCCATGAGTCT | 9886 |
rs527943994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898473 | AAATTTTAGTAGGGG[A/G]GCAGCCCAGTGTGTA | 9886 |
rs527950865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942360 | ATTTCCACCTGTGTG[A/G]TCACAGAGCCTGTGT | 9886 |
rs527984215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943025 | TCAAAGTCAGGGCGA[C/T]TCTTCTGGTCTTAAC | 9886 |
rs528033717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985293 | CAATACTCTGGGGAA[A/G]AAACTCAATAATGTG | 9886 |
rs528038859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992881 | GCCCCACAGAGAATG[C/T]CACAAATCCACATAA | 9886 |
rs528074532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895141 | AACTATGTCACATCA[A/G]TATCTAAATGCATGA | 9886 |
rs528082226 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950743 | TAAAAACGGGCTCAT[C/T]ATGAGGCCCCTTAAA | 9886 |
rs528094333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981833 | GGGGTGCAATGGTGC[A/G]ACCTCGGCTCACTGC | 9886 |
rs528104346 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973682 | ATAATGGGAAAAGAA[C/T]ATAGATTCAAACTGA | 9886 |
rs528113740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900941 | AATTTCATAACATCA[C/G]AATAATAATGCATTA | 9886 |
rs528138378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938930 | AAATGCTAGTTTATT[G/T]TTATCACAGCAGTCA | 9886 |
rs528176576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924979 | AAGTGTTTAGATGAC[A/G]GGGATAGATCACTCA | 9886 |
rs528212879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974094 | CTCCTAATATCTAAA[A/G]TGTGTGGTGCAAATC | 9886 |
rs528214209 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925515 | AACCTTATAATATAT[C/T]GTAAAGAACTAGAAA | 9886 |
rs528225178 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002572 | TGAAGGGCTAGAGAT[A/G]GCTATTATTTTTAGC | 9886 |
rs528236520 | snp | C/T | 0.000362588 | 0.0134597 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888392 | CCAAATCCTTTTCCT[C/T]TTCATCCAGTTGTCC | 9886 |
rs528256961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911912 | TCACGTTGGCCTGCT[A/G]GCAAGTCCGGTCACC | 9886 |
rs528267110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951808 | TGTTAATAATGGTAA[A/T]TGATTTGGGAGGCCA | 9886 |
rs528268243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994653 | GCAATGCATTTTATT[A/G]TACATTAAATTCATT | 9886 |
rs528288482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900066 | CCTCCTGGAGGAAGG[A/G]ACCATGCCATTCTGC | 9886 |
rs528294479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906292 | AAAGGACTCATGCTC[C/T]GCTACTTAATGGATG | 9886 |
rs528303831 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945055 | AGGACAGAACCAGGG[A/G]TAGTTTTCATGCATT | 9886 |
rs528305810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952108 | TAAAACTTTTATAAG[A/G]TGAGTTAGTTATAAT | 9886 |
rs528345102 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925108 | ATGCTCTCTCTCCCT[A/G]TTGCTCCTCCTCTGG | 9886 |
rs528358841 | in-del | -/TT | 0.110872 | 0.20771 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918751 | TTTCTTTTCTTTTTC[-/TT]TTTTTTTTTTTTGAG | 9886 |
rs528440078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996987 | CTTATCAATTTATTT[C/T]TGTGGTCCAATAGAA | 9886 |
rs528455905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907338 | TTTTTATAAGAGCTC[C/T]AGGAGACAACTCTTG | 9886 |
rs528476387 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997684 | AACTAATGATAAGTA[G/T]TAAAAGGCTGCTTGA | 9886 |
rs528481002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953840 | GACACATGAAAAACC[C/T]TTTGAAATTCACTTT | 9886 |
rs528483750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907755 | CACAAATCCAAAAGA[A/G]CAAATAGAAATCCAG | 9886 |
rs528522026 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896332 | TAAAAATAATTGGGA[C/G]TGGTGAGTGTGATGA | 9886 |
rs528565623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939843 | ACCAAAGCCTTATGA[A/C]GTTCAAAAGAGAAAA | 9886 |
rs528584892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933319 | ATACCAGTCTGGAGT[A/G]CGACTAGAAATTTTA | 9886 |
rs528633573 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990536 | AATTCTCTCCTGACC[A/T]GTATTCTCCATCCGT | 9886 |
rs528693268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882054 | TTTTTTAAAAAAGCC[C/T]GTTTCTGTGATTTCA | 9886 |
rs528737288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952989 | GTTCATTCCTTGGGA[A/T]TTCCTTAACAAATTA | 9886 |
rs528760183 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870534 | GTGACAAGCCTGTAG[A/G]TGGCAGGAGGGAGTC | 9886 |
rs528778025 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912929 | GGCTGACAAGCAATG[C/G]AAGTCCATTGTTAAA | 9886 |
rs528794818 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869806 | TGGATGCATTTGTAA[C/T]TATCCCTACTCTACT | 9886 |
rs528795274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875841 | TGAAGCTAGGCCATC[C/T]CTTGCCTTTGTAAGG | 9886 |
rs528812338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873362 | GGCAAACGCAACAGA[C/T]TGGGGTCCCACTTGC | 9886 |
rs528815198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906898 | CCACCCAAATCTCGA[A/T]TCGTAGCTCCCGTGA | 9886 |
rs528859728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882101 | GCATGACAACAGAAA[A/G]ACCTTTATTTATAGC | 9886 |
rs528869457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982659 | TGGGCAAAATTTCCT[C/T]CTATTGGGAACCTCT | 9886 |
rs528874191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897029 | CAAAGATAGCATGTG[A/G]AAGATTGGCAAGGAT | 9886 |
rs528907737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975196 | AGAATCATAATCAAT[A/G]AACTGGTTACCAAGT | 9886 |
rs528910555 | snp | A/T | 1.66366e-05 | 0.0028841 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888526 | TGCATTTCCCTGTGC[A/T]TGCCAATGAACCCCT | 9886 |
rs528910676 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896180 | AAACATTCATTCCCA[G/T]GTGGAGACTGTTCAA | 9886 |
rs528919183 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880705 | TTGTGCATGCTAGAT[C/T]ATCTGCAATACACAG | 9886 |
rs528962804 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948601 | TGTCATTGGCTATTT[A/G]GGAGAAATTATCCTG | 9886 |
rs528973759 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926145 | GGGAGGCTGAGGCAG[C/G]AGACTCACTTGAACC | 9886 |
rs529021902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882789 | CTGTATTGTACTTTC[C/T]TAGTTCAGAAAGGGA | 9886 |
rs529027366 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889092 | CTTGATACCAAACTG[C/G]TCAAACACGCTTGTT | 9886 |
rs529044775 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879513 | AATTTATTTTATTAA[-/T]TTTTTTTTTTTGTAG | 9886 |
rs529057786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906764 | GTGTCTGAAGGTTCT[C/G]TGACCTGCAGACAGA | 9886 |
rs529078657 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968471 | ATATCTCTTATGTTG[C/T]AGACACAGAGCTGGG | 9886 |
rs529104499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900609 | CGCACACAGTGTAAG[A/G]AAACAGGCCCTCAAT | 9886 |
rs529104759 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966475 | AGGAGTTTGAGATCA[C/G]CTTGGGCAACATAGC | 9886 |
rs529109078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989454 | GTACATATAAGATAC[A/G]TTGATACTTGTTGAA | 9886 |
rs529129414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946327 | GCAATCAGTCCTCTT[C/T]ATTACAAGCTATTTC | 9886 |
rs529130293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938971 | GGTCTACAGTTGGGT[A/G]CCAATTCAAAGGAAA | 9886 |
rs529132106 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995669 | TCTTAGGAGAAATAA[G/T]AAAGGGTTGAATGTA | 9886 |
rs529154617 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895375 | TGCTCATTATTTTAC[A/G]CTGAAAGCAGTTAAA | 9886 |
rs529167460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939476 | GACCCTTCCCTTAAA[A/T]GCTTCCCCTTTCCTT | 9886 |
rs529221426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981885 | AGTGATTCTCCTGCT[G/T]CAGCCTCCCAAGTAG | 9886 |
rs529276221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897085 | CAAAGTTGGGACCAA[C/T]CTTTGTTGGAGGATT | 9886 |
rs529311356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948648 | AGTTACAGAGAAATT[C/T]TGGGGACTAGTACTA | 9886 |
rs529339604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930027 | TGCAAAGAAGTAAAT[A/G]AAACAATTGAAAGGA | 9886 |
rs529350227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940709 | GGGTTGAAATTCTAC[A/G]TTCTGTCCTTTCCCA | 9886 |
rs529356058 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985515 | TCAGAGTCCACATGT[C/T]AATTTCCTGTACAAA | 9886 |
rs529387061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933769 | TAACTTTAGAAGTCC[A/T]AACACAGGAGATGGA | 9886 |
rs529387572 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947094 | AAATGCAGCAAGTAG[A/T]ACAGACCGTATTTTG | 9886 |
rs529429632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876489 | CTAGTCTGAGATTGA[C/T]CACAAACCTTGTTGG | 9886 |
rs529437642 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997789 | TAAGATGTTCTAATG[-/C]CTGCTACTCAGGATT | 9886 |
rs529442446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969511 | AAGGAGCTTGTCAGG[A/G]CATCAAAGAGGAAGT | 9886 |
rs529469236 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969230 | ACCTAAACCCAACTG[C/T]GCAGATACAGGGTGC | 9886 |
rs529479683 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961803 | GTGGTGATTTATAAC[C/T]TTTTTTTGTTTTTTT | 9886 |
rs529492416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953991 | TTAACTCTATTCCAT[A/G]TTATTGTGGTTTAAT | 9886 |
rs529495422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912963 | AGAAAAGTGGGTGGG[C/T]GGTCATTTTTAAGGA | 9886 |
rs529557429 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954696 | GAGGAGAAAAATTGG[A/T]TGGAAGGAAATGTGA | 9886 |
rs529594909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947918 | CAGAATGGCTGCACC[A/G]TTCACATTTCCACCA | 9886 |
rs529611910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914122 | CAAGCAGTAACTCAC[C/T]GAAAATTAAAGAATA | 9886 |
rs529612121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907366 | TTGAGTTGAGCGACA[C/T]CCCTTTAAGAAGAGG | 9886 |
rs529624605 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997813 | CAGGATTGGTCTGGG[A/C/T]AACCTAAGGCTCTTT | 9886 |
rs529647025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987129 | CACAACCTAGTGATT[A/G]TATCAGTGAAACAAA | 9886 |
rs529665645 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001279 | GCTCTCGCGTCCCCA[C/T]GAGCCTGCGGATGTG | 9886 |
rs529685072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905151 | TCCAGATAATACTTA[A/C]AAAAAAAAAAAAATT | 9886 |
rs529692040 | snp | A/G | 0.0001821 | 0.00954026 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892971 | GGGATTAGCAATCGA[A/G]AAACAGAGGACCACA | 9886 |
rs529713908 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955484 | CAATATAACAAGAAT[A/G]CTTCCTTCTGATTGA | 9886 |
rs529793090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937069 | CTAAAAAAGGAAGAA[A/C]AGGTACAAGTATTTA | 9886 |
rs529804367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872681 | CGCAATGGAATACTT[C/T]GTGTCGCATGTCAGA | 9886 |
rs529834833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964320 | ACTGATTATAAACGC[C/T]CTCCTGGGTTTTGGG | 9886 |
rs529834949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971924 | ACATTTATGAAGCCA[A/G]TAAACATGAAAAAAA | 9886 |
rs529850405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878952 | TGGATTTTTGGAACA[C/T]TGACAATTATAAACA | 9886 |
rs529859689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923103 | TATGGTTATCCAAGT[A/G]TTTGGAATATACTTC | 9886 |
rs529864300 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879512 | TAATTTATTTTATTA[A/T]TTTTTTTTTTTTGTA | 9886 |
rs529875682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916354 | TGCAAAGCCATCTTG[C/G]ACCTTCCAGCTCAGC | 9886 |
rs529898715 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989496 | TTACTCAGCCTTATC[A/T]CTCTCCAGTTGCCCG | 9886 |
rs529915321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957547 | GCAGCCACCACCAAG[A/C]CTTACGGTCAATACA | 9886 |
rs529930424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957138 | CCTGAAAGACCAGCC[C/T]AAGGCTGTTTGACAC | 9886 |
rs529976995 | snp | C/T | 0.00119737 | 0.0244387 | nc-transcript-variant, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000931 | GAGGAGCTGCAGATG[C/T]TGCGCCTACTTTCAG | 9886 |
rs529981626 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906672 | GGACACATGCAGCAC[A/G]TAGCACAGGCCTGGT | 9886 |
rs529996076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918378 | CATGGTGTTCTGTCC[C/T]TCTCTTATGAAAGAG | 9886 |
rs530000752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910300 | TTCTAGAGGAGTTTT[C/T]CCATTACTAGATTTT | 9886 |
rs530014655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916879 | ATGGTCCTTTAAATG[C/T]GGAAGAGGTAGGCAG | 9886 |
rs530041354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874126 | ACCTAAGACTTAGTA[A/C]GTCATTGTCTTAACA | 9886 |
rs530105555 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952215 | ACTGTCTTTTATGGT[A/G]TTATCTGTTCTACTG | 9886 |
rs530117949 | snp | C/T | | | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872119 | TCCTTTCCAGGGACA[C/T]AGAAGATAAAAGCTT | 9886 |
rs530143822 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945750 | TGTTTAAGCCATTCC[C/T]ACGGCAGTATTTTTG | 9886 |
rs530150972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959337 | GTTTCCAGGGATGTA[G/T]GAGAAAGCAAAATCC | 9886 |
rs530154767 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956190 | CTGGATTGAATCCTG[C/T]AGGCAATTGTAACAC | 9886 |
rs530172501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906352 | AATAAAGAATTTAAG[A/T]GGAACACTGGAATAT | 9886 |
rs530187538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960242 | ACTCTGTTAAGTACT[A/G]AGTGAAAAATCTAAT | 9886 |
rs530246748 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003424 | ATTTATAATCCTTTG[G/T]GTATATACCCAGTTA | 9886 |
rs530249768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995415 | CCCAAGATATCATTT[C/T]CAAAATTAGTGGTCA | 9886 |
rs530250542 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972692 | AGTATAATAAAAAAA[G/T]AAAAAAAGAGAGAAA | 9886 |
rs530311196 | in-del | -/G/GG | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953772 | GAGGTGGCTAATGAT[-/G/GG]GAAAAAAAAAGCATA | 9886 |
rs530334536 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959724 | ACACTTTATCTCTCT[C/G]GGCCTGTTTCTGCAA | 9886 |
rs530349030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917680 | ACCTCTCCAACAGCC[C/T]GCCTCTTAATACAAT | 9886 |
rs530349708 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977003 | TTTTTTAAAATCTTA[A/G]CTTCATTGGCTAAAT | 9886 |
rs530369222 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887325 | AACCACTTACTAAAT[A/G/T]TGTAATGCCCTGGCA | 9886 |
rs530374753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965846 | GGACATCTGATAGGA[C/T]ATTGTCTTGCCTTGT | 9886 |
rs530375894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973250 | CATATCTCAGGGCAG[A/G]TAAGATTTTAGTGGT | 9886 |
rs530391538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987746 | TAAACTTTTCAAGTA[C/T]GCTTTCCAAGATCTG | 9886 |
rs530402788 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931540 | TATGGCTGAAAAATA[G/T]TCTTAGACATATTAC | 9886 |
rs530409521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893742 | AGAAAAACTGCTTTA[C/T]AGTAAATTTTGACAT | 9886 |
rs530427498 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980332 | TCCGCTGGACCAATT[A/C/G]GTAAGTTGAACACAT | 9886 |
rs530448479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900031 | AGCAAAGGCCCGAGG[A/T]AGGAGCCTGCCTGTG | 9886 |
rs530491147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995135 | AACTAAATTATTTAT[A/G]AGTATATCAAAGAAA | 9886 |
rs530512463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900462 | TCTGCTTCCCTGTTC[C/T]GGGAACTGACACCTC | 9886 |
rs530567970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886857 | ATGTGTATTTTTGTA[C/T]AATTTTGTGTATGTG | 9886 |
rs530682430 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951715 | TCCATCCCCATGGTG[A/C]TTTGAATGGCACTTT | 9886 |
rs530684186 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000983 | CAGCCCAGATTCTTA[C/T]CTTTTCTGACTGACA | 9886 |
rs530687890 | snp | G/T | 1.67492e-05 | 0.00289384 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911016 | GAGAGAGAGCATCTG[G/T]GCTCGGTGTCAGTCA | 9886 |
rs530708687 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001753 | GGCGCGTGGGGCTCC[C/T]ACTGGGACCCCGGTC | 9886 |
rs530723836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905244 | TCACAAGGTCAGCAG[C/T]TCGAGACCACCCTGG | 9886 |
rs530731831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965704 | ATTCTTCAGGATTTT[C/T]CCATTACCTTAATTC | 9886 |
rs530745137 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922427 | TATGGAGCCTCTACA[A/G]CAGTACCAGAAACTA | 9886 |
rs530786077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905706 | TCCTGGTCCACTTGA[A/C]GTTTCACTGTGCAAC | 9886 |
rs530798821 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916063 | ATGAAATAAGGCCAC[A/G]GCAGCAACTCCCATC | 9886 |
rs530873725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901233 | CTTATTCTCTCTAGG[C/T]TGAGGGCAGAGGCAT | 9886 |
rs530899780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912864 | GCCTTTTTGAGGGAG[A/T]CTATTGTTAAACTAA | 9886 |
rs530902672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996197 | TTTGATCATGTTCTC[C/T]CCACTTACATATCAA | 9886 |
rs530938445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875318 | GTTCTGTGCAGGATG[A/G]TAACTCCTGGCCACA | 9886 |
rs530939355 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952067 | TGTCACAGCCCCCCA[-/C]CCCCCCAAAAAAGAA | 9886 |
rs530989613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973428 | GCATAAACTGTATTT[A/G]AGCCTTCTTAACAGC | 9886 |
rs531020855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887475 | AAAAATAGTCCAAGT[C/G]TAAGACAGTACAAGC | 9886 |
rs531035523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947173 | CACTGTCATGAGTTT[A/C]TCTCTGCTCTTGTTA | 9886 |
rs531083275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924940 | AAATTGTAATCCCCA[A/G]TGTTAGAGTTGGGGC | 9886 |
rs531104206 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918419 | AGTTCTGCGCATGCC[C/T]ACTCCCTCACTCACA | 9886 |
rs531125612 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927899 | TAAAGAGACAATCCA[C/T]GGAATGGGAGAAAAT | 9886 |
rs531142846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874884 | GACAGATGCAACAAT[A/G]GAATGTTTTATCAGC | 9886 |
rs531150101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974042 | GGATAAAAAATAGTC[A/T]TCAGAATTTTCTATC | 9886 |
rs531176812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872159 | GTGAGGAGAGCTGGA[C/T]GAATGGGGGCCTCAC | 9886 |
rs531187744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899283 | CTGAAGTAAAGAAGG[C/T]TTGCTAAACAGACGA | 9886 |
rs531207418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909290 | TTTCGTTGTTTGAAA[C/T]GAATACATTTCATTG | 9886 |
rs531216257 | in-del | -/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884926 | ACATTTTTTTTGTCC[-/T]TTTTTTTTTAGAGAC | 9886 |
rs531224700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925415 | AACATTCCAAAACCT[A/G]TGGAACACTGCACAA | 9886 |
rs531243125 | snp | C/T | | | nc-transcript-variant, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000936 | GCTGCAGATGCTGCG[C/T]CTACTTTCAGAAGAC | 9886 |
rs531331180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963224 | CCCTCCGCTCCATAC[A/G]GAGACCCAAATGGCT | 9886 |
rs531342485 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910131 | AAATGAAATGTGTTC[A/C]TTTATAATTAAGTGG | 9886 |
rs531342963 | snp | A/G | 8.47045e-05 | 0.00650731 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871686 | GACCATAAGACCTGC[A/G]GTTCATTGATGCCTT | 9886 |
rs531353341 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910110 | GATATCTACGTTCTA[A/C]ACTGAAAATGAAATG | 9886 |
rs531360899 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956118 | ATAGCCTACTACACA[A/C]CTAGGCTATATGGTA | 9886 |
rs531398284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964311 | GAGGATACAACTGAT[G/T]ATAAACGCTCTCCTG | 9886 |
rs531398953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903852 | CACATAGTGATTTAC[A/G]TTTTCAACGAGACTA | 9886 |
rs531400958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949513 | AAAGCTCCTATTTTC[C/T]TCCCACTGTTCTGGG | 9886 |
rs531427499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999109 | AGTGCACTTTCACCT[C/G]TACCAACTTGTTGTC | 9886 |
rs531430501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977371 | AACATGTCACTTATG[C/T]ATGGCTGCTTATGCT | 9886 |
rs531436877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942510 | GATCAACTGGTTAAA[C/T]CTTTTTCCCATTAAT | 9886 |
rs531485498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927996 | CAGAAAAAAAATCCA[A/G]TTTAAAAATGGCAAA | 9886 |
rs531520607 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976492 | ACTGAAGTACAGCCC[C/T]GTCTTGTTCCTTTTA | 9886 |
rs531539122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884647 | ACAATGGGATACTAT[A/G]TAGCCCTAAAAAAGA | 9886 |
rs531550198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930169 | AATATATTTACCACA[A/T]CTTTAAGAAAAAAAA | 9886 |
rs531597279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962574 | AAGAAGCAAATTATA[C/T]AGTATTTTTTTCTGT | 9886 |
rs531626873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928551 | TCATGTTCTCACTCA[C/T]ATACAGGAGCTCCAA | 9886 |
rs531631841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972104 | TGGGAGTGTAAATTA[A/G]TTCAACCATTGTGGA | 9886 |
rs531674166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965082 | ATTTGTTCAACCATT[C/T]AACATTCGTTGAGTA | 9886 |
rs531674508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877574 | GCACTTATTATGGAG[A/G]TAATGTTGACAAAAT | 9886 |
rs531683132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922571 | AAGAATTGGCCCAGG[A/C]AGTAGGGAGACATTC | 9886 |
rs531699994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923211 | CTTGAAGCATAGACA[C/T]GTACAAGCAATTACC | 9886 |
rs531715503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886002 | TATGATGACCACTCA[C/T]GGAGCCAGTTTAAGG | 9886 |
rs531717080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952960 | TTGTGGGAAAACACA[C/T]AACGCAAGCTTTAGT | 9886 |
rs531721679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978993 | TCTCCCCCTATGTAT[C/T]ATGTGTCACCAGCAA | 9886 |
rs531740382 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916925 | GAGAAATATGAAGTT[G/T]CTATACTGCTGGCTT | 9886 |
rs531752345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885647 | ACAGGAATGCGGCTT[C/G]TCAAGGTCCCCTGTC | 9886 |
rs531779059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992989 | AGGAAACTAAGGTTA[C/G]CAGGAATAACTTGCT | 9886 |
rs531786802 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970223 | GGTTATTTGTGGTTA[C/T]AAGTCTATTCCAATT | 9886 |
rs531801155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899013 | GTTGGTTCTACCATC[A/G]TAGTACAAATATCAT | 9886 |
rs531853287 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943142 | CCAAAGGCACAGCTT[C/G]TGTGCTAACGTGCAA | 9886 |
rs531882095 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879994 | ACAACTACTTACACA[A/G]CATTTGCATTGTATT | 9886 |
rs531883795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879589 | GCCTCAAGTGATCCT[C/T]CTGCCTTGGCTTCCC | 9886 |
rs531894972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929734 | TAAAATGAAGAAAAC[G/T]TTTTAAGTATAAGGA | 9886 |
rs531914244 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930177 | TACCACATCTTTAAG[-/A]AAAAAAATGAAAACA | 9886 |
rs531950672 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60985933 | TTCATGTGCTTCTTG[A/G]TTATTATAAAACCTA | 9886 |
rs531980020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910207 | ATTCATTGAGAGAGA[C/T]GTTAAGTTATGGTGG | 9886 |
rs531993174 | snp | A/C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987051 | GATGTGAGACAAAAC[A/C/G]GACAGCTGCACAGCC | 9886 |
rs532002955 | snp | C/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953364 | ATATCCTTGCTGAAG[C/G/T]CCCGGCTTCTCTCAT | 9886 |
rs532010095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957041 | ACATTTTGCTATATT[C/T]ATAACAATTTTGTCT | 9886 |
rs532036558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899065 | AGAAGGTTGTGGGTT[A/G]TCATCCAATGAAATC | 9886 |
rs532036784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905006 | AAAGCACATGCATTG[C/G]TAACTTTCTTCCCTT | 9886 |
rs532068903 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000870 | GGGGCTTTCACGGCT[A/T]ACAAACCAAGAAAAA | 9886 |
rs532133404 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993755 | CATATAAATAAAATA[A/T]ATAACATTTATAGGT | 9886 |
rs532152370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970979 | TAAAACTTCAGAGAA[C/T]TTTTGTGACGATTCA | 9886 |
rs532172518 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953605 | AAGAAATCTATCACA[-/C]CTGTTGTTTTTATAA | 9886 |
rs532187105 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884847 | TAGGGGGTGAATGGG[A/G]AAAGGAAAGCCATCT | 9886 |
rs532190990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971388 | GCCTCAGAAATAATG[C/T]CACACATCTACAACC | 9886 |
rs532208946 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943288 | TGCAGCTAACAGTAG[A/G]ATCTAATGATATATT | 9886 |
rs532225164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993109 | GAATGATGGAGGGGA[C/T]GTGTCTCTCTGCTTG | 9886 |
rs532245716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936514 | CCTATATTTAAGATT[C/T]CATGACTCTATTATG | 9886 |
rs532254548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943963 | AGCACTCACGACACA[A/G]AACCTACCCTGAAGC | 9886 |
rs532258938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964301 | TGGCGCCAGAGAGGA[C/T]ACAACTGATTATAAA | 9886 |
rs532260269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986289 | TGACAGTCAAATGAG[A/G]TAATGTTTGGAAAGG | 9886 |
rs532300296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921957 | CCTTTCACCAAATGG[G/T]AAGGTGGTGGTGGGG | 9886 |
rs532305506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878832 | GTGGAGAGCTGTAGA[A/G]GTGGGCATGGATTAA | 9886 |
rs532317333 | snp | C/T | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877943 | GGCAGGCAAAATCTG[C/T]TTGCCAAGGCAATTA | 9886 |
rs532334854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916282 | AGCAGGGATGAGAAT[G/T]CACATTGAAAACCGC | 9886 |
rs532413361 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966005 | AAATATATAATTTTA[A/G]AAACTGTGATGGGGA | 9886 |
rs532416857 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924805 | TCTTTTCTGACCACA[A/T]CGGAATAAAACTAGA | 9886 |
rs532418418 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965738 | TGGTCTATCCGTAGT[C/T]GGGGAATAAAGTCAT | 9886 |
rs532429758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915463 | AAAAAAAGAAAAGCC[A/T]GAAAGAATGGACACT | 9886 |
rs532454654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958477 | ATAGGGCAAAACTTG[A/G]AATTGAAACACTATA | 9886 |
rs532466046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917558 | TCTTCTTGTGGTGTC[C/T]TCACATGACAGGCAG | 9886 |
rs532494147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916999 | CCACAGAAGCTAGAA[A/G]AGGTAAGGCAACAGA | 9886 |
rs532524331 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880387 | GAAACTTTCTTTGTT[A/G]TTCTCCTATGCAGCC | 9886 |
rs532530289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911613 | CAGAGCAATCAAAGA[C/T]GTAAGAGGTTCAGGG | 9886 |
rs532530874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972590 | ACCTAATGTAGATGA[C/T]AGGTTGATGGGTGCA | 9886 |
rs532544288 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886717 | TTTTTTTAAGAGATG[G/T]GGGGGGGGGTGGGTC | 9886 |
rs532562152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879740 | TACATCTTTATAACA[G/T]GGTTACATCTATATA | 9886 |
rs532592033 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922166 | CAAGGGATTCTCAGC[A/G]CTTTTTGGTGAGTCA | 9886 |
rs532614778 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960741 | AGCCTCTTGGGCTGC[C/T]CTGGCAGCTACCCCT | 9886 |
rs532643511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936928 | CATAGCACTGGGAAA[A/G]ACATATACTTGCTAC | 9886 |
rs532646893 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874693 | CCTCCCCCAAGTGAT[A/T]TTCCTACATATGAAG | 9886 |
rs532689035 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001855 | CTTCCTGGAGGCCTC[C/T]CCAGGACCCACCCAC | 9886 |
rs532758848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979083 | AGGTAGGTATTTTCT[C/T]GAACCAGGTTCAAGG | 9886 |
rs532926475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875955 | AGCATTGCATTTGTT[C/T]TTCTAATCCAGCACA | 9886 |
rs532930844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883450 | ATTAGCATTCGTGAG[A/G]TCAGCTCTGACAGTG | 9886 |
rs532955088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969618 | TAGGATTTTCTATCA[A/G]TCAGAACAGCCTGAA | 9886 |
rs532983617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901900 | CTCTTGGGCCCATCA[A/G]TGCTTTTCTGGGCTG | 9886 |
rs533004446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895440 | ACGGAGTTTTGCTCT[A/T]GTTGCCCAGGCTGGA | 9886 |
rs533043544 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871203 | ATAAAAAGAAACAAA[A/G]TAACAGACTAAAGTT | 9886 |
rs533071532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933686 | AGCCTAGGTGAGAGT[C/G]AGAATCCGTCAAAAA | 9886 |
rs533076316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914171 | TAGCTGATCTTAAGC[A/C]AAGAAGACAGAAAAA | 9886 |
rs533080637 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876749 | TGATGCCTCAACTCG[C/T]TCTTTCTATCTAACT | 9886 |
rs533093984 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876517 | TGGGCAGATTTGGCT[A/C]CAAATTACATTTGAC | 9886 |
rs533117888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990068 | GCTCACTGCAAGCTC[C/T]GCCTCCTGAGTTCAT | 9886 |
rs533125501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984118 | CATATTTTTGCTCCA[A/G]TTGGGTAGGCAAGAT | 9886 |
rs533134589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896263 | GAAACAGGCAAGTTC[C/T]AGCATTTCTATTTCT | 9886 |
rs533150476 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947889 | GCTAAATAAAAAACT[G/T]CTAAACCATTTTCCA | 9886 |
rs533158991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898295 | TTTTCCCTGCTGGTA[A/T]CTGAGGTAGGTTCTT | 9886 |
rs533172885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985248 | GGAGAGTAAACTGTC[C/T]ATTTCAAATAATTCT | 9886 |
rs533179995 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963879 | AGGTAACTCCTCAGT[C/G]AATAAATGATTGGGT | 9886 |
rs533185423 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946047 | GCTGGGCGCGGTGGC[A/G]CACGCCTGTAGTCCC | 9886 |
rs533193797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939785 | AAATGGCAGAATTTC[A/T]AATGTTTCCAGCCAT | 9886 |
rs533288890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977452 | AAGAAAACAAAAGGA[A/G]GAAATGAAGGCAGAA | 9886 |
rs533294776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884174 | TGATCTTCTCAGCCC[C/T]TGCTATCCAAGGCTT | 9886 |
rs533303441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975244 | CAGGGGAATTCGTCA[C/G]AATGTGTAAATGGCT | 9886 |
rs533305400 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983070 | GGTCTATTCTCAGTG[C/T]TCTTGAATCTGTCTG | 9886 |
rs533322651 | snp | C/T | 0.00206697 | 0.0320813 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871444 | GGTGGATCAGATTAC[C/T]GATTGGTTTCTGTTT | 9886 |
rs533333013 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929178 | AATTGGATATGAGAT[A/T]TGGGTGGGGACACAG | 9886 |
rs533343058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890786 | TTGACAAAGGTGGAA[A/G]GGAAGTTCAGGGAAG | 9886 |
rs533350677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962262 | TTGGAACTAAAATTA[A/T]AATAATCTGGTTGTC | 9886 |
rs533384596 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897942 | AACTCCTGACCTTGT[C/G]ATCTTCCCACCTCGG | 9886 |
rs533385733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955328 | TTACAGGCATGAACC[A/T]CCACACCCAGCCAGC | 9886 |
rs533392161 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942647 | GAGCTTGTGTTTATT[G/T]TCTAGCAACCAGTGA | 9886 |
rs533480909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928598 | GAAGTAGAGAATATA[A/G]TAGAATGGTGGTTAG | 9886 |
rs533506249 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914202 | GTTTTGGGTGTGGAG[C/G]GGGCAGGGAGGAGGT | 9886 |
rs533532439 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907924 | ACCTTTTACTCAATG[A/G]TAGCACCAAGATCAT | 9886 |
rs533569003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908592 | AGAAATTAAACAGCT[C/T]TCTCAGAGCCGGGAA | 9886 |
rs533598476 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876566 | AAATGTATCCTCAGG[A/G]ATAATTTATAAAACC | 9886 |
rs533600450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948141 | ATCTGCTCAAGTCTT[C/T]TGCCTATTTTATAAT | 9886 |
rs533610511 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940372 | GGGAGAAGGGAAGTA[C/G]GGGAACAGAAGAGAG | 9886 |
rs533626311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903094 | ACCTCACCTGGATTC[C/T]GAAGGTGACAGAGAG | 9886 |
rs533648761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908090 | TTAAATCATAAGAGA[A/G]CAATAACACTGTGGT | 9886 |
rs533656096 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998270 | TATTAGCCATTCACA[C/T]GTGTCTTTTATAAGA | 9886 |
rs533688810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941547 | ACGGGCACCACTCTG[A/G]TGCCTAAAGTGAAAA | 9886 |
rs533726336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997338 | TTTGTCAAAATGCAG[C/T]TGTGTGGGTGCAATC | 9886 |
rs533726772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883024 | ACAGATGAGGAAACA[A/G]GTTTAGAGTGAGCCA | 9886 |
rs533734260 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871242 | CTCCTAACAAAAAAA[A/G]TATACATATCAGTTT | 9886 |
rs533742019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907503 | AAAAGTGGATATAAA[A/G]TAGGTGGTGGAAAAA | 9886 |
rs533767276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960746 | CTTGGGCTGCCCTGG[C/T]AGCTACCCCTAATGG | 9886 |
rs533772254 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870811 | ATATTTGATATCACT[A/G]TATTTTACATGGCAC | 9886 |
rs533775797 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985630 | CCAAATGACTCAAAT[C/T]CTAAACCAGATAAAA | 9886 |
rs533787392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919412 | GATTTCATTATTCTG[A/G]GCTTTTAATCAGCAG | 9886 |
rs533811057 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982213 | CTAGTCAAGTATTAA[C/G]TGGGTCACTCTACTC | 9886 |
rs533822687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920060 | TCTTCTACAAATACA[A/C]CAGGGAACCTCTCCT | 9886 |
rs533837420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896641 | AGAAAGCCAGAATTA[C/T]AAAGGACTTAAGGAT | 9886 |
rs533916935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877796 | TCTACACAAGACAGT[A/C]CTATTTTGGGTGATA | 9886 |
rs533966441 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934926 | TCAACAGCCGTGGGC[A/G]TGTTATATGAGACAT | 9886 |
rs533986481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963366 | AATATTCTGACTACA[A/G]TAAAAGAGATCCTGA | 9886 |
rs534008689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882485 | AAAATATAAGTAAGA[A/T]ACAATGTTTTCCTGA | 9886 |
rs534033626 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957367 | AGTAATGTGTGGTGT[C/T]CAGATGGCTGTAATG | 9886 |
rs534048693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998702 | CTTGGCATCCAAAAT[C/T]CTGGAACTGTCTCTT | 9886 |
rs534049676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961359 | GATGTATTATGTGAC[C/T]TTGCTGAAGCTCTGC | 9886 |
rs534121341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940832 | GTGGAAAATGCTGAA[C/T]TTCTCATAAATGTAC | 9886 |
rs534122100 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870285 | CTCACAATAGCACCA[A/T]TTCCTAGACTCTTGG | 9886 |
rs534137038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984284 | GAAGTCTGTTCAGCA[C/T]AGTAATCACCATTAC | 9886 |
rs534189548 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954115 | GGCTCTACAAATACA[A/G]TGAACATTAGCCTGG | 9886 |
rs534211254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876888 | GAAAGTCAAGTGCAG[A/T]TAGGACTGGTTGGTT | 9886 |
rs534232565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921388 | AAGGATGGTGCCTCT[C/G]ACAGGCAGAATCAGC | 9886 |
rs534250550 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979337 | AAATAATAAGGAAAG[A/G]AATATGGCTAAAATG | 9886 |
rs534253031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955759 | AGTTTGAATGCAAGG[A/G]AAACAGGAACCCATA | 9886 |
rs534272231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922017 | GGGCATAGGATTGGA[A/T]TGGATTTAGAAAAAC | 9886 |
rs534300632 | snp | A/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999899 | TGCAGCTTATTTTAC[A/G/T]ATTCTCTGCTGTTGC | 9886 |
rs534301599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972954 | TGCAGTGTCGAAAGC[A/G]AGAATGATTTTAGTT | 9886 |
rs534309886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991621 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 9886 |
rs534310723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915522 | ATCTTACTCAAAACT[A/G]ACTTGAACGTTATTT | 9886 |
rs534327989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966182 | ACATACCAAAAAACT[C/T]TTAATATTAGTTTTC | 9886 |
rs534332551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880126 | TGGATTTGGCTGTCT[A/G]AGTTGGGGGGGTGGT | 9886 |
rs534384318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898003 | GCCACCGCGCCTGGC[C/T]GCTAATAATTATATT | 9886 |
rs534384571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890452 | CTGGCACACAAGGCC[C/T]ATTTACAACCTAATC | 9886 |
rs534423413 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897397 | TGTCACAAAAGTACT[A/G]TCTTCTTAGTTTGAC | 9886 |
rs534424823 | in-del | -/CTT | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000408 | AACACCAGGGGAGAC[-/CTT]CTCACCAAGAGCAAG | 9886 |
rs534435000 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002375 | TTTACTCTTCTTTTT[C/T]ATTTTCCCTTTGATA | 9886 |
rs534453521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966967 | AAGCACGACAAAGTT[A/C]TTGGGGAGAAATATT | 9886 |
rs534459414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874343 | CCACTTCATTCTCAG[A/T]ATAATCTGTAAGGTT | 9886 |
rs534461059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883730 | CAGAATAAGTCCAGC[A/G]GCAGCTACTATTTAT | 9886 |
rs534470207 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926059 | AACATGGTGCACCCC[A/G]TCCCCCGTCTCTACT | 9886 |
rs534478809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927547 | GAGAATAGAGAACCC[A/G]GAAAAAAATTCCCAC | 9886 |
rs534506317 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944450 | GCTCTACGCAGACCC[G/T]ACGGGCCCGGGCACG | 9886 |
rs534506809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920880 | CAGGGTGGTCTTGAA[C/T]TCCTGAGCTCAAGCG | 9886 |
rs534509416 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951854 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC | 9886 |
rs534566998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886292 | AGCTTCAACCAAGGC[G/T]TCTGCTCCCATAGCC | 9886 |
rs534588266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930706 | GAACCTCCTAAAAAA[G/T]TCTCTTTGAAATGTT | 9886 |
rs534589064 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922613 | TGCCCATAATCTGGA[A/G]TAATGAGAGCCACAC | 9886 |
rs534593372 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897536 | TTATCTAGAAGCTTC[A/G]GATCAGGTAAATTTT | 9886 |
rs534648773 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924417 | AAAGAGACAAAGAAG[G/T]TCATTATATAATGAC | 9886 |
rs534678305 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946569 | TTCTGATGTCTTGAC[A/G]GTTGCATTTGCACCT | 9886 |
rs534678914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981628 | TAACCAATTAATCAA[G/T]ATCTCATATTAATCA | 9886 |
rs534689493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917832 | TCTGTCTTGCAAATT[C/T]TAGTCATTCCTTAAA | 9886 |
rs534702213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887938 | CATGGGTTCAAATCC[C/T]GGCTCTACCATTTAT | 9886 |
rs534705580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938669 | CAGAAGAATAACTTC[C/T]ATACTCCGACATCTG | 9886 |
rs534725755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894809 | AATAGTTCTAATTGG[C/T]GCCTTCTATTTCCCT | 9886 |
rs534747039 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890440 | ATACCCTTTAGGCTG[G/T]CACACAAGGCCCATT | 9886 |
rs534766017 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953367 | TCCTTGCTGAAGGCC[C/T]GGCTTCTCTCATGCC | 9886 |
rs534865194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906006 | CATGAAACTAGACAT[A/G]CAGAAACCATAGCTC | 9886 |
rs534925730 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996819 | GTATTTGAAATCCAG[A/T]TTTAACTAGGCATCC | 9886 |
rs534946910 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967582 | TTTTTTTCTTTTTGT[G/T]GTTTATGTCAAGGAG | 9886 |
rs534949188 | snp | A/G | 0.000449509 | 0.0149851 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910874 | CAACCACGCTGTACT[A/G]GTCTTGGTTTACCTG | 9886 |
rs534953497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900844 | ATACCTCTGGTATAC[A/G]GCAGAGGTTAACCGG | 9886 |
rs534990935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989785 | CCTAGGCTCCCTCCA[A/C]CCCTGCTCTCTCCCC | 9886 |
rs535043187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988706 | TATTCAATCCACCAC[C/T]GATGGGCACCTAGGT | 9886 |
rs535067649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967043 | TTTGGGAAAAATAAA[A/G]CAGGGTGGGGGTGAG | 9886 |
rs535070297 | snp | G/T | 3.33133e-05 | 0.00408112 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888672 | CGGGCCCTCCTCCCT[G/T]TCTTCCTCTGGGTCG | 9886 |
rs535088035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932662 | TTGGTCAAGTCTTTA[C/G]AGATGGCAAAGATGT | 9886 |
rs535104759 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967797 | GTGTTTCTATATTTT[G/T]ATTAATCCAAATAAA | 9886 |
rs535138488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960456 | GCCCCTTAGAGAACT[A/G]GAAATTTAATAATCT | 9886 |
rs535170501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974541 | TTTCTACACATCCAT[C/T]GAGATTGGGGGGTCA | 9886 |
rs535180695 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003175 | ATGAGTGAGAACATG[A/C]GGTGTTTGGTTCTCT | 9886 |
rs535190078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919177 | AATGATGCTATTGCA[C/T]GGACACTACATTTTC | 9886 |
rs535240298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875434 | ACAGCCACATGTGGC[C/T]GCTGTTTGGACCATC | 9886 |
rs535300109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973008 | CTTAAACCGTGACTA[G/T]AGAAGTAAATATTTC | 9886 |
rs535306827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938399 | AGACTGTGTCACTTA[C/T]TAACTATGAGAGTAG | 9886 |
rs535327733 | in-del | -/TTCCAAGTCT | 0.183568 | 0.241012 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003348 | GGACATTTGGGTTGG[-/TTCCAAGTCT]TTGCTATTGTGAATA | 9886 |
rs535332418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931311 | TATCCCCCAAAGAAA[C/G]CTTGTGCCCACTAGC | 9886 |
rs535339489 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945461 | CTTTGGCTTATCCCC[C/T]CAAAAACAGGATGCG | 9886 |
rs535355586 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938644 | AAAATTTACAAAGTA[C/G]AAACAAACCCAGAAG | 9886 |
rs535363296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924519 | TAGAGCTAAAGAGAG[A/G]GAGAGAGAGACCCTG | 9886 |
rs535446555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881612 | TCTCACCCTCAGTCT[C/T]TTCATCCGTTACATG | 9886 |
rs535469311 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913630 | GTTGTCACTTGGTGG[A/G]GGGTTGAGGAGGGAG | 9886 |
rs535508014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896479 | AAAGCATAAGAATTC[A/G]AGAATGCAGAGGCAG | 9886 |
rs535532303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912387 | TACAGGTGCCCACCA[A/C]CATGCCCGGCTAATT | 9886 |
rs535590821 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927311 | CAACTGACTCAAGTG[A/T]TAATCTCCTTTGGCA | 9886 |
rs535622789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975755 | TCTTCGAAATGTTTC[A/C]TTTTGGCAAAAGCTA | 9886 |
rs535635804 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894658 | AACTCTGCTATAAGC[C/T]TCATCCTGAACACAA | 9886 |
rs535649690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981295 | GGTCAAAATAATAAA[A/G]ATGATGAAAATAATA | 9886 |
rs535669651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940847 | CTTCTCATAAATGTA[C/T]CATTGATCCCCAATT | 9886 |
rs535674306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894074 | TATGTAATGAGAAGA[A/G]TCAAGTCGATGAATC | 9886 |
rs535685377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882050 | CTGATTTTTTAAAAA[A/C]GCCCGTTTCTGTGAT | 9886 |
rs535699404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887798 | GAATTGGTCAGAGAA[C/T]AGATTCTGAAGGGGA | 9886 |
rs535707407 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964373 | ACATGGAAAATAAGC[-/AA]AGTCTCTCAAGCCAA | 9886 |
rs535741957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947243 | GCTTGCTGATAGAAT[C/T]AGTACCATTCCTTTA | 9886 |
rs535756658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925060 | TCACACAAGATCTGG[G/T]CATTTAAAACTGTGT | 9886 |
rs535767212 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886765 | CTGGATTTAAACTGC[C/T]GGGTTCCAGCAATCC | 9886 |
rs535833129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892542 | TATACTTTTCAAAGT[A/G]CTTTTAATCACACAC | 9886 |
rs535840320 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935599 | ACACCAGATGATCTA[A/T]ATGATCTGTGCAGAA | 9886 |
rs535856233 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876475 | AAGCAAAACTGGTAC[C/T]AGTCTGAGATTGATC | 9886 |
rs535869411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891978 | GCATCCGCCTTTGCT[C/T]GGTTCTCATTCTTCT | 9886 |
rs535873399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959064 | AATGCAAAGTTGCCT[C/T]AACGTTCAAAAATCA | 9886 |
rs535881604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978573 | AACCCGTGCTGGGAC[A/T]GTAGCATGGCTGTGA | 9886 |
rs535882448 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933517 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 9886 |
rs535894922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933378 | TTCATCCAATTTTAA[A/G]GTTTTATTCCTGGAA | 9886 |
rs535903524 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929191 | ATTTGGGTGGGGACA[C/T]AGAACTAAACCATAT | 9886 |
rs535917828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885748 | AGACATGCTCCTCTT[C/G]TACTTGGTTTTGATA | 9886 |
rs535959014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920112 | TACTTCTGCACAAAG[G/T]CCCTTTCCTCGTGCC | 9886 |
rs535978390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922788 | TATGGAAAAAGATTC[C/T]CTCTGTTCTGCTTTT | 9886 |
rs535991729 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964016 | TGTCTCACAACATTC[G/T]CTACCCCCAAATTCA | 9886 |
rs535999369 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999355 | AAATCTAGAGTTGTC[G/T]ACCTAAAACAACAAC | 9886 |
rs536016211 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980316 | CAAAAATCAATAAAT[-/G]TCCGCTGGACCAATT | 9886 |
rs536040596 | snp | C/T | 3.32906e-05 | 0.00407973 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872340 | TTTTCTAAAGAGGGG[C/T]TACAAAGAAATTGGG | 9886 |
rs536051017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956187 | TTACTGGATTGAATC[C/T]TGTAGGCAATTGTAA | 9886 |
rs536074504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946582 | ACAGTTGCATTTGCA[C/T]CTGGGGTTGTCTGTG | 9886 |
rs536081453 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895032 | GACCTGTAAACAAGT[A/C]CAGACAGGACCTTGG | 9886 |
rs536087967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949774 | TTCCTATGATTACCC[A/C]TTTAAAGACAGAAGC | 9886 |
rs536107437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895667 | CCTTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 9886 |
rs536136055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992429 | AGGACAAAGTCCACA[C/G]ACATGCTGGAGGGGA | 9886 |
rs536157559 | snp | G/T | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903980 | CTTTTCTTTTTTTTT[G/T]GAGACAGGGTCTTGC | 9886 |
rs536160317 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940034 | TTGATGAGGTCTTGG[A/C]CTGTAATGGGATCTT | 9886 |
rs536171827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962573 | GAAGAAGCAAATTAT[A/G]TAGTATTTTTTTCTG | 9886 |
rs536174719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993237 | CAAAGGTCTACTGCT[A/G]ACAAAAATTACAATA | 9886 |
rs536228624 | in-del | -/ATTC | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949973 | GTCCTTTCTGTGTGG[-/ATTC]ATTCATTCATTAGGT | 9886 |
rs536276836 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944689 | CCCCTAGGAGCTGAC[A/C]GGCCGCGGACTCCGA | 9886 |
rs536349118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899684 | GTAATTGAGAACCTA[C/G]TGTGTACCAGGCATT | 9886 |
rs536352742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937902 | AGCACCTACTATGTG[C/T]TTTACATGCATGAGG | 9886 |
rs536390179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979247 | CTAAGAATTTACCCA[A/G]TGTTTTGATCATGAT | 9886 |
rs536434101 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966676 | TTTTTTTTTTGGTTC[-/T]TTTTTTTTAATCTTT | 9886 |
rs536435575 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976101 | ATGGGTCAAATAAAT[A/G]TAAATGGGAATAATA | 9886 |
rs536437155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949098 | CATTAATGCTAAGTA[A/T]TGATGGGTCATAAAG | 9886 |
rs536439969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925696 | AAAAAAAGAAGACCC[A/G]AATAAATAAAATCAC | 9886 |
rs536505270 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957845 | CCACTGTACGGACAG[A/G]AAAGCTGAGGTATGG | 9886 |
rs536505457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997120 | AGCTTTTGCTACAAT[A/G]AAACAAATGTCATCA | 9886 |
rs536512161 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904613 | CTGAGGTTTGGTAAC[A/G]AGTATCAGAAAATTC | 9886 |
rs536514264 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950201 | AACATGTATGTCACA[A/C/G]CTCTAGAAAAGAAAA | 9886 |
rs536517181 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942856 | GAAACCACCGATAAC[A/G]GTATTTTTTTTTTTT | 9886 |
rs536553768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943558 | GTGCAAGCGCCAAAG[C/G]GGCTAGCGTATTCCC | 9886 |
rs536564233 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001080 | CGCGCGCGCGCACGC[G/T]TGTGTGTGTGTGTGT | 9886 |
rs536607717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994102 | TATGTGTTAGGATAA[C/T]ACTAAAAAACCATAT | 9886 |
rs536642964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972390 | GTCTTTTGCAGGGAC[A/G]TGGATGAAGCTGGAA | 9886 |
rs536679835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951885 | AACATGATGAAACCC[C/T]GTCTCTACTAAAAAT | 9886 |
rs536751774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905810 | TAAGAGCTAACTCAA[A/C]ATGCTGTATCTAGAC | 9886 |
rs536786042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965495 | TCCCTATTTGTGTGC[C/T]TAGCATGGTGCCTGG | 9886 |
rs536800492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993335 | TTCAGGCTCAGCTAC[A/G]AGGGCACATGCCAAA | 9886 |
rs536826758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964736 | TCTTAATGAAGTTAG[C/T]TTGTATAGAGAAAAA | 9886 |
rs536830773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879811 | GCACACAAACACACA[C/T]ACACACTCAGGCACA | 9886 |
rs536838924 | snp | A/G | | | intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60898681 | TACTTTACCAATAGC[A/G]TGAGGCTTCTTAAGT | 9886 |
rs536842688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950399 | AAATTACATTTATGT[A/G]TCACAGCACATTTAA | 9886 |
rs536851156 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899237 | GCTTAAACAGTCCTA[C/G/T]TTAACTCCTGGTCAA | 9886 |
rs536858194 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965390 | ATTAAGTCCTCAGTT[A/T]ATAGATGAAAAAAAT | 9886 |
rs536875660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943687 | CCAGCCTGCTAAGGG[C/T]GCCTGTTGTACATTT | 9886 |
rs536909686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892627 | GTTCTGACACCAGAG[A/T]TGATGGTGCCTGTTA | 9886 |
rs536940959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986706 | TATGAGTACGACTGA[C/T]TACCTAATATAAAAA | 9886 |
rs536952438 | in-del | -/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002299 | CAGACCTTCCAGTGG[-/T]TCAAGATGATCTAGG | 9886 |
rs536958247 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972378 | GGATGAGTTCCTGTC[C/T]TTTGCAGGGACATGG | 9886 |
rs536969755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954239 | ACTTCTCTGAGTCCA[A/G]TTTCCTCCTCTGTAA | 9886 |
rs536974028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978763 | TTTTTCTTTTTTTAA[C/T]AGAGCATTGTTATTT | 9886 |
rs536978390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987225 | CCATCTCAAGAAACT[C/T]CCCTGAATTTTCTTC | 9886 |
rs536983507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873425 | ATCACTAGGTTAGGG[G/T]CTAATGAATGAGCAT | 9886 |
rs537044521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900792 | ATGTGAGCCATTACA[A/G]TTCTTCAGACTGTTA | 9886 |
rs537077566 | snp | C/G | | | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945067 | GGGGTAGTTTTCATG[C/G]ATTCACATAAATGCT | 9886 |
rs537084975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937963 | GGGGAGGGGATGCTG[C/T]TCCCATTTTACAGTT | 9886 |
rs537099177 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908808 | CAGGACGCCTGGAGG[C/T]TGTGAGGAATTGGAA | 9886 |
rs537106265 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940687 | GACTACATAATCTCT[C/G]CCTGTTGGGTTGAAA | 9886 |
rs537157597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931886 | CAATTCTACCTCAAA[C/T]AGAAGATGAAAAATT | 9886 |
rs537161115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924237 | GAAATAATGATACGA[A/G]TGACTATAAATTTCA | 9886 |
rs537191046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972770 | ACACAATACCAGTAG[C/T]GGTGGATTAAATGGC | 9886 |
rs537233542 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879603 | TCCTGCCTTGGCTTC[C/T]CAAAGTGCTGGGATT | 9886 |
rs537255280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880626 | TTTCCAGCACAACCT[C/T]GACAACAAATAGAAC | 9886 |
rs537274562 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897152 | ACATATCTTGGCCCT[A/G]GCTAGACTTTGAACA | 9886 |
rs537307329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936619 | GTAACCACTATTCTT[C/T]AGAACCTCATGACTC | 9886 |
rs537314059 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944355 | TTCGCGGCTATTTAT[A/G]TCCACACGATTGGAT | 9886 |
rs537339863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911703 | GAAGTTCGTACTAAG[C/T]CTAATTGACACTCAA | 9886 |
rs537344672 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937090 | CAAGTATTTAAAAAA[A/T]ATATCAAAGCAGTAG | 9886 |
rs537357685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994835 | CAAGTAAATTCTAGG[A/G]CCCAGACACTTTAAT | 9886 |
rs537367094 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939393 | TTACAAACTAAAAAT[-/A]AAAAAAATTATGATG | 9886 |
rs537396838 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998474 | CATATTAAACAAATA[C/T]AAATAAGAGACTTCG | 9886 |
rs537403343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995498 | AACCTCATTTTATCT[C/T]ACTGTTTAAAAGGCT | 9886 |
rs537441822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952267 | ACCCATGAAAAGGCA[A/C]TTTGAGATCATAAAA | 9886 |
rs537525167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938539 | AACTGTTTAAGATTG[C/T]GACAACTTCCATCAA | 9886 |
rs537550246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934614 | GTTCATTGTTGACTT[C/T]TGTTTGATATACACA | 9886 |
rs537572689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981466 | ACACAGCTTGAAGGT[C/T]GTAAAGCTGAAATGC | 9886 |
rs537595221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920692 | GCTTGCTCTGTCACC[C/T]AGGCTAGAGTGCAGT | 9886 |
rs537600716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913909 | GGTTGTTGTGAGGAT[C/T]ACGTGAACTGATGAA | 9886 |
rs537622789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874172 | GGAAGCCAAACCCAA[C/T]AGGCCGAAGAAAAGA | 9886 |
rs537624037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876709 | TATATTGGTTAAAAA[C/G]AGTTTTTAAAAATAA | 9886 |
rs537630413 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969791 | TATTACATCATAATA[G/T]GACTTAGCTTTTTGG | 9886 |
rs537644085 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938231 | AATTCTCTTATCAGC[A/G]TTTCTGGATGTACCT | 9886 |
rs537655700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958876 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGGCACCG | 9886 |
rs537701350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951986 | TTGCTTGAACCCAGG[A/C]GGTGGAGGTTGCAGT | 9886 |
rs537716199 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959523 | CAGTGCTAGTGGATG[C/T]TGCTCACATGTCTCT | 9886 |
rs537739107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914305 | AGAATAAAAATAGTA[A/C]TACCTAACCCTCTTC | 9886 |
rs537773524 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931005 | GAAGCAATATTGAAG[A/T]CTTCCCTCTGCAACA | 9886 |
rs537775706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908217 | TCCATGCCAAAGAAT[A/G]TTTGAGGGGCAACTT | 9886 |
rs537805947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915768 | CATCCTATACCTGCC[C/T]GCTATTATTGCTGTC | 9886 |
rs537824065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963606 | TTTAAAACATGAGGT[C/T]ATGTGTTCCATTGGA | 9886 |
rs537829097 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955469 | ATCAATCATGCACAG[A/C]AATATAACAAGAATG | 9886 |
rs537882641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902916 | CAAGACACCAGGCCA[C/T]GTATCGGGGATAGAA | 9886 |
rs537884318 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932193 | TTGTAATCTTTACTT[A/T]GGCAGACGTCTACAC | 9886 |
rs537895105 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898246 | CAAAGATTCAAGTAG[C/G]AGTGTCTGACCTTCT | 9886 |
rs537922744 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977889 | CACACTAAAATAAAT[A/G]TTCTGCATGATGAAG | 9886 |
rs537966042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984675 | TTTAAGTTATTTATG[C/T]ACACATGGTAATATC | 9886 |
rs537970918 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999958 | TCATAGGATGTGAAC[G/T]GAACTCGTTATTTTG | 9886 |
rs538023827 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870881 | TTGTAAATACACATT[C/G]TTGGAGTTGACTTTG | 9886 |
rs538026595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961459 | CACCATTGTGAATAT[C/T]TTACATGAACATATA | 9886 |
rs538060889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876111 | AACTATTTGGAACTA[A/C]ATTTCCCAGAGAAGT | 9886 |
rs538086653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935260 | TGATTTCATTTATAT[A/G]AAGTCCAAAAGCAGG | 9886 |
rs538093055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928235 | GAATGCAAATTAGCA[C/T]GGCCATTTTGGAAAA | 9886 |
rs538105884 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918674 | TTGCTGTGAATCATC[A/C]CGCCATTGGAATATG | 9886 |
rs538161102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998090 | CTCTGCCGTAAAATA[C/T]GGGGTTGTACTAGGT | 9886 |
rs538174716 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922098 | GTTAATAATATTTAT[A/T]TATAAGGGTCTCATA | 9886 |
rs538238077 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930650 | TAGCTGCTTATGAAT[-/A]GAGAGGCATGGCTTA | 9886 |
rs538242784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898649 | TGCCCTGGATGTGAG[A/C]AGATAAATCAAGTTA | 9886 |
rs538275106 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954718 | GAAATGTGACAAAAT[C/T]ATTTTTGAAATTACC | 9886 |
rs538299099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949835 | TCTGTGAAGACAAAG[C/T]ATCTTTTCCATTGCA | 9886 |
rs538304161 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976622 | CTATGCCCAATTAAG[C/T]AGACATTGTCCAACA | 9886 |
rs538306310 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950847 | CCCCAATTCCTCCCT[A/C]CCCAAATGCTGACTG | 9886 |
rs538313496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999443 | TTACTCTAGGATGTC[A/G]GTAAACAGAAGAACG | 9886 |
rs538344021 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890938 | ATCTTCTTAGAATTG[C/T]TCTGTAGAAGGCACT | 9886 |
rs538347420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985445 | GGAAAAAGAGAAATG[C/T]CACGCACAGCAATCT | 9886 |
rs538371471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990046 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 9886 |
rs538377007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872761 | GACTGTCCTATACCT[C/T]TCCTTTGGTTACATA | 9886 |
rs538406153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985342 | GATTTTACTCACTTG[A/G]GATGACTCTAGTTCT | 9886 |
rs538413488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914921 | AGGGATAATATGTAA[A/G]GGAAAATAAAAGGCA | 9886 |
rs538421124 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906933 | CACATGTCGTGATGT[C/T]GTGGGAGGGACCCAG | 9886 |
rs538429761 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871709 | GATGCCTTTTATGTG[C/G]TAGGCCTTGAGCTTA | 9886 |
rs538457747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877705 | ACCTAACAGGGCCCA[A/C]CACAGAGTGGGTGCT | 9886 |
rs538463303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891332 | GTTGTTGTTGCTGTT[C/T]GCTTTTTTTTTTTTT | 9886 |
rs538503262 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933142 | ACTTCTTAAGATCTC[C/T]TACTTTATTTGAAGT | 9886 |
rs538550741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908904 | AAACACAGGAGTGTT[C/T]CTGAAGCCCCTCAAT | 9886 |
rs538574768 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878000 | GGAGACAACTGCTTG[A/G]TATAGAGATAATCCA | 9886 |
rs538585742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885144 | GGACAATAATGTATC[A/G]TATATTTCAAAATAG | 9886 |
rs538623322 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891422 | CATGGCCCACTGCAG[A/C/G]CTTGTCCTCCCAGGT | 9886 |
rs538627169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941955 | TTTCTCTTTTTCCCC[C/T]GAGAAAGGGAAGAAT | 9886 |
rs538668713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950561 | GCCATCTCACTAACT[A/G]GGATGTAATTCTGTG | 9886 |
rs538700682 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896866 | GAGATCTTGTTTCAT[A/G]GAGGAGTGGGAGTGA | 9886 |
rs538704917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951113 | CAAGCATCTGTAATA[C/T]ACATGTCATTTAATC | 9886 |
rs538821139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955188 | TAGCTGGGATTACAG[A/G]CGTGCACCACCACTT | 9886 |
rs538843929 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876105 | AGATTGAACTATTTG[A/G]AACTAAATTTCCCAG | 9886 |
rs538883062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885290 | GTACCCCATAACTAT[A/G]TATAATAATTATTAT | 9886 |
rs538889795 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922179 | GCGCTTTTTGGTGAG[A/T]CACTACTTCGCTGGA | 9886 |
rs538890044 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929780 | AACAAATATATGGAA[C/T]AAAAAATCAGAATAA | 9886 |
rs538929023 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922654 | CCAAGGTGAAGAGAG[A/T]AGGGTGGAGGAAGAA | 9886 |
rs538936798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998991 | TGAAACACAGACAAC[A/G]CCTGCCTCACCAGAT | 9886 |
rs538938553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991665 | CTCAAACTCCTGACC[C/T]TGTGATCCACCCGCC | 9886 |
rs538980423 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872937 | CTCCCCAGACCTGGT[A/G]GGCCTGCTGCGATCC | 9886 |
rs538996748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000142 | ATTAGTTAATCCTTA[C/T]GCTTCCGAGTGCATC | 9886 |
rs539040420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957756 | TTGTCCAATGGTAAT[A/G]ATATTTATTGAATGC | 9886 |
rs539045449 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872793 | GAAGAGCAGGCGGTA[G/T]GGGCAGGGTGGAGAG | 9886 |
rs539068695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953180 | GGACAACATGGGTAA[A/G]GTTAGCCTCCTCGTG | 9886 |
rs539106979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946636 | CCTGCTTTTTAACAG[C/T]CTGCTTTTCCTCAGT | 9886 |
rs539120341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993437 | TTCTATTATATACAT[A/G]TGCATATATTCATGT | 9886 |
rs539189491 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870682 | AGCGCACTAATGGTA[G/T]CTTATGTATTCAGGT | 9886 |
rs539203217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971268 | AAGAACAAAGCTGGA[A/G]GCATCACGCTACCTG | 9886 |
rs539227211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963792 | CACTTTCCAAATTAC[A/G]AGTTCCCTGAAATAT | 9886 |
rs539241788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971626 | ATACCATTCAGAACA[C/T]AGGCATGGGCAAAGA | 9886 |
rs539243363 | snp | C/T | 6.72914e-05 | 0.0058001 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888584 | CAGGAACTGCACCCT[C/T]GGCTTCCAGCCCCAG | 9886 |
rs539247403 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919974 | TTTAAAAGATGCATG[-/A]AAATTCCAGGGCAGA | 9886 |
rs539288726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932573 | GGATTTTGGAGGCCC[C/T]ATCGTCCTCATGGGG | 9886 |
rs539294895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925220 | CAGCACCATGCTTCA[G/T]GTAAAGACTGCAAAA | 9886 |
rs539296668 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966661 | TTATTGAGAAACTTC[-/T]TTTTTTTTTGGTTCT | 9886 |
rs539328602 | in-del | -/TTTTA | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997427 | AGCCTTCCAGATGAT[-/TTTTA]TGCCCTCTAAACTTT | 9886 |
rs539373780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913072 | GTTTAATTCATCTGA[C/T]TGAGAAAAATGATAA | 9886 |
rs539387571 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872457 | GGCCATGGCTCCAAT[A/G]CCAGCCAATGTAGTG | 9886 |
rs539415890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975912 | TGCACCTCATGATCT[A/G]TAAGGGGATGGTGGA | 9886 |
rs539439280 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966844 | CCTCCCCCCTCCCCC[C/T]ACCCCACAACAGGCC | 9886 |
rs539476642 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907441 | CTATGTATGGTTTTG[C/T]TCCTGACATTTTAAA | 9886 |
rs539477378 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993458 | ATATTCATGTGTAAG[G/T]ATATATAAAATATGA | 9886 |
rs539505779 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881159 | TTCTCTCTCTCTTGC[C/T]TGCTGCCATGTAAGA | 9886 |
rs539536025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997252 | CTGGGGAAATTAAAA[A/G]GATATCAAAATTGTG | 9886 |
rs539547533 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959495 | ATGTGATTGCTCTAC[A/G]CATCACAGGCAGCAG | 9886 |
rs539565484 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911757 | AGTACAAAAACATGG[C/G]ACTGTTATTTTGACC | 9886 |
rs539570073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907468 | TAAAAGATCCAGAAA[A/G]GAGCTTCAAAAGTTC | 9886 |
rs539606290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982154 | TGAGAAATTAAATGG[C/T]GGCCCATGAACTTTG | 9886 |
rs539624749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881641 | TGGGAGGAATTTGGA[A/G]TAGATGCTATTAAAA | 9886 |
rs539645511 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974434 | ATACAATGAATACTT[A/T]AGTTCACTATGAACA | 9886 |
rs539680360 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944832 | TGGGTTACCTTCCTC[C/T]GCGACTTGGCGGGAG | 9886 |
rs539733540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990705 | TCTGTGGGCTCATCT[G/T]TCACTACTGGGCCAT | 9886 |
rs539737033 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919261 | CATTAAAAAATACTA[C/G]TGCAACAAATTTTAG | 9886 |
rs539759762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967951 | AAGTTCCATTATGCT[A/G]GTAGAAAAGGGGTCT | 9886 |
rs539774750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983570 | TTTATTGATTCAGAT[A/G]TAATACTAGGCTGGA | 9886 |
rs539824730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969856 | AATAGAATAATAATA[A/C]CTTGGATGATAATGG | 9886 |
rs539835676 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946871 | CATGTTGGAATTACC[G/T]AGTTGAATGCCTAAA | 9886 |
rs539870438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939368 | AAGAGGAGGAAGTGG[A/G]TTCTATTTGTTTACA | 9886 |
rs539887379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927527 | AGACACACTGACCAA[C/T]GGAAGAGAATAGAGA | 9886 |
rs539924968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920771 | GCCATCCTCTCACCT[C/G]AGCCTCTTGAGTAGC | 9886 |
rs539941838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914432 | CTTTAAATGTCCTCA[A/G]TGGTGGGAAACCTTA | 9886 |
rs539961141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921375 | TCTCCAGGAGAGAAA[C/G]GATGGTGCCTCTGAC | 9886 |
rs539964463 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962054 | CTGAATTGATCCGCC[A/G]GCCTCGGCCTCTTAA | 9886 |
rs539974770 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990230 | CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 9886 |
rs539976231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975091 | TTTACAATAAAAATA[C/T]GTCCATCAAGCTAAT | 9886 |
rs539990155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982976 | AACTTTTATTGTTCC[A/G]TGGTCTTTTAATCGA | 9886 |
rs540071631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902092 | TCAGGCATAGGAATC[C/T]CAGCTCTTCTGTTTT | 9886 |
rs540089730 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931705 | TTTTTTCAAAACTAT[A/G]TGTATATATAAAGCA | 9886 |
rs540091058 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946133 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 9886 |
rs540100659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933451 | CATTGGCTGGGTGCG[C/G]TGGCTCACGCCTGTA | 9886 |
rs540128990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955189 | AGCTGGGATTACAGG[C/T]GTGCACCACCACTTC | 9886 |
rs540148140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979259 | CCAGTGTTTTGATCA[C/T]GATTCTAATTTATCC | 9886 |
rs540209341 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871374 | ATCAGTGCCCGAAAC[C/T]TGAACTATGTCGTAT | 9886 |
rs540216993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962124 | ATTTATAATGGCTTT[G/T]TTTTTGTACCTGAGA | 9886 |
rs540249265 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871001 | ACAAAAGGATAACCC[C/T]CTAATTACGTAATAA | 9886 |
rs540268611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895220 | CACCTCAAAATAATG[A/G]TAGTTAAAGAAAAGA | 9886 |
rs540270537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901791 | AAAAGTAAAAGGAAC[A/G]CAGAACATAAGACAT | 9886 |
rs540276342 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956268 | TATGAATAAAAGACT[-/A]AAAAAATGGTATGCC | 9886 |
rs540285604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889302 | CCAGTCAGGCTTTTA[A/G]TCTCTGGAAAAATCT | 9886 |
rs540289556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933009 | AAACATTTATGAGAC[G/T]ATCATATGCTCGTTA | 9886 |
rs540299002 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893300 | TCTCAGTCCTGGAAC[C/T]ACAACATGCTGAACT | 9886 |
rs540307072 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950007 | CTGTTGGGGTAGGGT[A/G]AGTTTGGTAAAAATG | 9886 |
rs540322212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982639 | CATTACCAAATGCCT[C/T]CTGATGGGCAAAATT | 9886 |
rs540324437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926038 | GAGCTCAAGACCAGC[C/T]GGACCAACATGGTGC | 9886 |
rs540343947 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898547 | AGGAGATGAATGGCC[A/G]TGTAAGCTCATACTC | 9886 |
rs540359343 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919980 | AGATGCATGAAAATT[C/T]CAGGGCAGATTTCAA | 9886 |
rs540400604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968525 | AGGTCCCTGCTATCA[A/G]TGAAACCTACTGAGC | 9886 |
rs540405383 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960032 | CTAATTTGTTCTGAC[A/G]TGGAGATTGGTAGGT | 9886 |
rs540419356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875881 | TGCCTCTGAGACTGA[C/T]GTGTGAGGGTACAGC | 9886 |
rs540420407 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933694 | TGAGAGTGAGAATCC[A/G]TCAAAAAAGAAAAAA | 9886 |
rs540427387 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945464 | TGGCTTATCCCCCCA[A/G]AAACAGGATGCGTGA | 9886 |
rs540438291 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952857 | CAACTTCAGGATTCT[C/T]GGGGTCCTTGACAAA | 9886 |
rs540454607 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902068 | TTCATCCTGGGGACA[-/T]AGGCTGGGTCAGGCA | 9886 |
rs540471156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912637 | CAAAGAATAATTTTA[A/C]CAGGAGAGTTACTTT | 9886 |
rs540476588 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003400 | TGCATGTGTCTTTAT[A/G]GTAGCATGATTTATA | 9886 |
rs540493514 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967778 | GGGCAAAGAGACAAT[A/G]CTGGTGTTTCTATAT | 9886 |
rs540496446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890008 | TTCATGTAAGCCTCA[C/T]AATAGCCCTGTGAGG | 9886 |
rs540507929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906659 | GTGAAGCAGGACAGG[A/T]CACATGCAGCACGTA | 9886 |
rs540510588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926952 | ATTATCCTTGGTTGC[A/G]GATGATATCTTATAT | 9886 |
rs540571819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907756 | ACAAATCCAAAAGAG[C/T]AAATAGAAATCCAGC | 9886 |
rs540587580 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991549 | AATTCTCCTGCCTCA[A/G]CCTCCTGAGCAGCTG | 9886 |
rs540599233 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954612 | GTTTGTTTAAAATTC[A/C]AGTGTCAGTGGTGTC | 9886 |
rs540601592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873710 | AAATTCCAAGTGTGA[A/G]CAACCAGTTTTGATG | 9886 |
rs540645224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947848 | CTGTGGGATGAATAC[C/T]GAAGAATGCAATTGC | 9886 |
rs540652623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957521 | AATGGTTCCCAGATT[G/T]GTGCAGTGGTGCAGC | 9886 |
rs540664237 | in-del | -/AT | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992063 | TCAGTATGAAAAGAC[-/AT]AAATTCAGTGAGAAA | 9886 |
rs540672125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000885 | AACAAACCAAGAAAA[A/G]TCAATCCCGCATCAC | 9886 |
rs540679908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914536 | TTTGGGAGAATGTTT[A/G]GACTTAGTAAAAATG | 9886 |
rs540706580 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972794 | AAATGGCAAGCTCAA[A/G]CTTAATCTAACTACT | 9886 |
rs540717720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910824 | TTGATTTGTAAACCC[A/G]CTGCTGGTTTTGAAA | 9886 |
rs540732999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902651 | CTCTCTCCTTTTTCT[C/T]CTGGGGGCAGCTGAT | 9886 |
rs540742584 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970876 | CTGAATGCTAAACAA[C/T]TCCTTGTAAAAATAT | 9886 |
rs540770203 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945251 | ACTGGGGAATAAAGA[C/T]ACAACTGTGTTCAGC | 9886 |
rs540777738 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929509 | ATAATTGAAAATTAA[A/G]TACTAAAAACAAACA | 9886 |
rs540799422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971412 | TACAACCATCTGATC[G/T]TTGACAAACCTGACA | 9886 |
rs540815887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878852 | GCATGGATTAATGGA[C/G]ATGTACACTGCGTAG | 9886 |
rs540821285 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912851 | ATTAATTGTAATTGC[C/T]TTTTTGAGGGAGTCT | 9886 |
rs540847474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882774 | TACAACTATAACCAC[C/T]TGTATTGTACTTTCC | 9886 |
rs540869329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919803 | GACCCACAGAAGATC[A/G]TGCTCTCTATGCTTT | 9886 |
rs540879125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879438 | GCCTGGGCTCAAGCA[A/G]TCCTCCCACCTCCAC | 9886 |
rs540899034 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885573 | ACAGTATTGTAGCAC[A/C]TGGTAACCTGAAGGA | 9886 |
rs540906037 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920426 | AGAATGAGAAGGGCC[C/T]GTTCAAGAGATGGGA | 9886 |
rs540969892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961759 | AAGTTATTTTTCTAT[G/T]AATATATTATTGCAA | 9886 |
rs541075828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917170 | CAATAAGAAACTAAC[A/G]TAGCACACTTTAGCC | 9886 |
rs541092124 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917868 | ACTCAGACATCACCT[C/T]CCCTGGAAAGATTTC | 9886 |
rs541094259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892066 | ATTTCCTGAGGCCTC[C/T]GCAGCCATGCTAAAC | 9886 |
rs541098863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905590 | AAAAAAAAACCAAAA[C/T]AGCAATTGTGATCCT | 9886 |
rs541105176 | snp | A/C | 2.14034e-05 | 0.00327128 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911311 | TGGCAACCAGCAATG[A/C]TGTGCCCTAGGGATG | 9886 |
rs541177255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911926 | TAGCAAGTCCGGTCA[C/G]CTGTAGGGCTGAACT | 9886 |
rs541212452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959279 | ACAGTCACAGTTCTT[A/G]CTCTTGGAAAACGGA | 9886 |
rs541222234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987521 | AAGCCCTATTTCCCA[C/T]TGACATATCCAAGGT | 9886 |
rs541262023 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922466 | AAGTAACCACATACC[A/C]GAAACTGGAAGGATT | 9886 |
rs541278042 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998080 | CTTCAGTTTCCTCTG[C/T]CGTAAAATATGGGGT | 9886 |
rs541293240 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894309 | AGCAGAAAATCCTGA[G/T]ATTAAAATATTTCCA | 9886 |
rs541293358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937605 | CTTGGTATTCGTTTG[C/T]AGCAGAAACTAAGGC | 9886 |
rs541307743 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922903 | GAGTCAGGTGAGGGG[A/G]TGCTGCCTCTTAAGA | 9886 |
rs541339604 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990856 | AGTTTATATCTCTGA[C/G]AAGCCCCACACCCAT | 9886 |
rs541374658 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963227 | TCCGCTCCATACAGA[A/G]ACCCAAATGGCTCAG | 9886 |
rs541403164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881253 | TAAACCTTTTTCTTT[A/G]TAAATTACCCTATCT | 9886 |
rs541410738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958983 | AAACTATTACTTTGG[C/T]GGTCTCCAGTGAGCC | 9886 |
rs541443035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973654 | TAGACTAGGAGAAAC[C/G]TGGTGGCCTGGGATA | 9886 |
rs541461840 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934478 | ACCATGGGAAAACAT[C/T]CTCTAATCTTTCCAG | 9886 |
rs541477015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874468 | AAAGCTGAATCTTGG[A/G]CCTTCTCTGGAAGAA | 9886 |
rs541489607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874708 | TTTCCTACATATGAA[C/G]CTGGTGCCTTAGGGG | 9886 |
rs541504746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995111 | CCCACATTATTAGAT[G/T]CTTTCTTGAACTAAA | 9886 |
rs541538259 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957500 | TGTAGTCTTCTGAGG[C/G]ACTTAAATGGTTCCC | 9886 |
rs541542031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988213 | TGCTGGGATTGCAGG[C/T]GTGAGCCATCACGCC | 9886 |
rs541575359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995729 | AGCATTTTGCTCACT[G/T]GTTTCTGCCCTTATT | 9886 |
rs541585752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967330 | CAGAGTCTCACTCTG[C/T]TGCCCAGGCTGGAGT | 9886 |
rs541633376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965593 | TCTTTGATTCTAAGG[C/T]AGTATTTCAAGTGCC | 9886 |
rs541636452 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944926 | AACCTCCTGCAAATG[A/G]CTGAGTGAGGAGGTG | 9886 |
rs541653844 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911998 | ACTTCATCACAAGAT[C/T]GCTCATTAGCCAATA | 9886 |
rs541664912 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945463 | TTGGCTTATCCCCCC[A/C]AAAACAGGATGCGTG | 9886 |
rs541668701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938053 | TCAAAATGAAAAAGC[A/G]TCGAACAGATCACTT | 9886 |
rs541683651 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909681 | AAGATAACAATCAAC[A/G]ACATTATAGAAAGAA | 9886 |
rs541686981 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879514 | ATTTATTTTATTAAT[A/T]TTTTTTTTTTGTAGA | 9886 |
rs541762531 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61001419 | GACGCTGGAAGCTCC[C/T]GCGGCGGCTCTGGGT | 9886 |
rs541771319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958261 | AAAGAACACTAATGG[A/G]ATTCTAAATTTTCTG | 9886 |
rs541771389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966215 | TGATGTTAGGATTAT[G/T]AGTAATTTCTTTTCA | 9886 |
rs541822954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952064 | CTCTGTCACAGCCCC[A/C]CACCCCCCCAAAAAA | 9886 |
rs541842554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882556 | TAGGCATATTTCACT[C/G]TTTTCTGGATATGCA | 9886 |
rs541849465 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959900 | ACAATTATGTAAATG[A/G]AGCACTTAACATATT | 9886 |
rs541851362 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002584 | GATAGCTATTATTTT[C/T]AGCAGAAATAATGCT | 9886 |
rs541859748 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945549 | GTCTTCAGTTTCCTG[A/G]TGAATTACCCTCCAG | 9886 |
rs541900230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912751 | TTGGTCTCCCCAGGG[A/T]CAGGACCCTCCACAA | 9886 |
rs541938465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919475 | AATAAACATCTCAGC[C/T]GGAATAAAGAATAGA | 9886 |
rs541973684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988903 | AGTCGCATTTATAGT[A/G]CTCTGGCTTTATTCT | 9886 |
rs541980435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972497 | CAATGAGAACACAGG[A/G]ACACAGGAAGGGGAA | 9886 |
rs541999281 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946839 | GCTCCTTCTAAAGGG[A/G]ATAAAGAACAGTCAG | 9886 |
rs541999505 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906900 | ACCCAAATCTCGAAT[C/T]GTAGCTCCCGTGATT | 9886 |
rs542003991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875716 | TCAGCCTCTTGGATT[C/T]TAAAGACTGGGGAGA | 9886 |
rs542055581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894385 | TCTGAATGTTCAGAA[G/T]CATCTTGAATAAAGA | 9886 |
rs542062164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873883 | ACACGGCCTTTGCCT[A/T]GGGCGGTGCCTGGTA | 9886 |
rs542093874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900874 | GTTAATCTCTATATA[C/T]TTTAATTATTTGAAT | 9886 |
rs542108960 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937117 | GTAGCTTTCTTCCGC[A/G]TATGTGATGAATTGG | 9886 |
rs542122079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917294 | GGCAAATTCTATTCA[G/T]TCTTTAAAACCTTAT | 9886 |
rs542138808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902037 | TCTCATTTGGCACTC[C/T]GCTTTCCAAGGACAA | 9886 |
rs542160788 | snp | A/G | 0.000166815 | 0.00913126 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911363 | TACCTCCTGGCACAC[A/G]CGGTACTGGTCAATC | 9886 |
rs542209588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967370 | CTGTCTTGGCTCACC[A/G]CAATCTCCACCTCCT | 9886 |
rs542249780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878143 | TGCTTATAAATATCC[G/T]GTGTGACTTGATATT | 9886 |
rs542251274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918944 | AGAGATGGGGTTTCT[C/T]CATGTTGATCAGGCT | 9886 |
rs542255620 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923421 | TGAAATATAAGGTCA[C/T]CAAATTGAAAGCCGT | 9886 |
rs542311275 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931021 | CTTCCCTCTGCAACA[A/G]CAATACATGAAAAAC | 9886 |
rs542380817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960965 | CATTGACTTGGGGTT[C/T]GTGGGGGTGGAGGGT | 9886 |
rs542388977 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869488 | AATAAAAAACACACA[A/G]CAAACCACCATGGTT | 9886 |
rs542452795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897802 | ACCTCCACCTCCCGG[A/G]TTCAAGCAACTCTCC | 9886 |
rs542466974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938758 | TTAGAGCAAATATAT[A/T]TTCAAGTTCTTAGAC | 9886 |
rs542479507 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891586 | ATCCTGGCCTCAAGC[A/G]ATCCTCCCACCTTGG | 9886 |
rs542498557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981772 | ACTTGGTATTATAAG[C/T]TACTTTTTTTTTTTA | 9886 |
rs542499203 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952328 | ACAAGTATGGGACTA[A/G]TGCACATGATAATAA | 9886 |
rs542503849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932149 | CAAACACATAAATAT[C/T]GATGTACACTCAGTG | 9886 |
rs542514562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890687 | AATATATAGGACAGA[C/G]ACTGGTCTTAGGAGG | 9886 |
rs542526590 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886997 | CCTAAGAAAATTAAA[A/C]ATAATTCCCTATTAT | 9886 |
rs542537457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973919 | AAGTAAAGGTTCTAA[C/T]GTTTGAAGTAGTTTA | 9886 |
rs542591270 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977337 | GCTTCATGGGGTGTT[G/T]CCCTATTTATGAAAC | 9886 |
rs542600453 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936254 | CCCCTTAATCAACTG[C/T]AACATAGGTTGGCCT | 9886 |
rs542637626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936888 | GTTGGTGAGTTCTCA[A/G]CACCTAGCCCCAGTT | 9886 |
rs542646430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929195 | GGGTGGGGACACAGA[A/G]CTAAACCATATCACC | 9886 |
rs542655163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971277 | GCTGGAGGCATCACG[C/G]TACCTGACTTCAAAC | 9886 |
rs542655616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963209 | AGGCAATTTTCATTG[C/T]CCTCCGCTCCATACA | 9886 |
rs542662596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878687 | CCTTGCTTGGGACTT[C/T]CAGGGGAGTATGACT | 9886 |
rs542672628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939329 | ATTTCTGTCCTATGG[A/G]CACAAGAAACAAAAG | 9886 |
rs542680270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937285 | TGCAGATGAAATGGG[A/G]AAATTGTGGTGTTTA | 9886 |
rs542698301 | snp | A/G | 1.65776e-05 | 0.00287898 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872141 | TAAAAGCTTCCATGA[A/G]AGGTGAGGAGAGCTG | 9886 |
rs542724259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930074 | AACAAAAAAATCTCA[A/C]CCCTTGGAAATTAAG | 9886 |
rs542734593 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997893 | ACTGGGTGGTCCTCA[C/T]TATTTTTGATCTGAG | 9886 |
rs542744869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978932 | ACCTCCTCTTCTTCT[A/G]TGATATGATAAATGG | 9886 |
rs542755251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923197 | GACCTATTAAAAACC[G/T]TGAAGCATAGACATG | 9886 |
rs542766915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984012 | GTCAAATATTTGACA[A/T]CTACCTGAAAACTAT | 9886 |
rs542789843 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969311 | TGTCACTCTGATATA[A/G]CAGCCACAAAAGCAA | 9886 |
rs542789926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971959 | ATCAACACTGGTCAT[C/T]AGAGAAATGCAAATC | 9886 |
rs542837116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941441 | AAGTCAATTATTACT[A/G]TATCAAGTTTCTTCC | 9886 |
rs542841759 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923453 | CTGGCAACAGTACAT[A/C]GTAGACTTGAAAATG | 9886 |
rs542842990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899463 | CAGTGTCAGCTACCG[C/T]GCTACATGGGAGGTC | 9886 |
rs542864323 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943033 | AGGGCGACTCTTCTG[G/T]TCTTAACTTCCTAGA | 9886 |
rs542871268 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884050 | TAGACACCATAAGAG[A/G]CCATCAGGATAACTC | 9886 |
rs542895900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999665 | GAACAAAACCACAGG[C/T]TGAATTCAACCTTAA | 9886 |
rs542922214 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973213 | TTCCTCTATCAAAAG[C/G]TTCTCATCTGTTAAA | 9886 |
rs543016502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964211 | TTAGGTACTTAGGAA[C/T]AAACATGTTACTGCC | 9886 |
rs543033050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872625 | GAAGGCACCAGCCCA[A/C]AGCAGAAAGCAGCGA | 9886 |
rs543033863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878790 | TGCATGCTGGAGTTC[A/G]CCAGAGAGCCAGGCA | 9886 |
rs543044784 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899297 | GCTTGCTAAACAGAC[A/G/T]AAGGTGAAATTGTGG | 9886 |
rs543085755 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968284 | GGGTGGTAAGTGGGC[A/G]TGGCATGTGGTCAGG | 9886 |
rs543093553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910160 | GGTAAAAAAAAAGTC[C/T]CCATTAATACAGAAT | 9886 |
rs543094101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916204 | CCAGAGGCCCTGCAG[C/T]TCCACCTTCTTCCTG | 9886 |
rs543094851 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899929 | GGAGGGCCTCGCTGA[-/G]AAGGTGACATTTCCA | 9886 |
rs543104847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885980 | TCCTTATGATTATGA[A/C]TAACAGTATGATGAC | 9886 |
rs543131938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910684 | TTTTCAACACAGTAC[C/T]TCCTCATTGGCAGGG | 9886 |
rs543142731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979751 | AGAGAAATAAATCAG[A/C]AAAGGGAACTAGGAA | 9886 |
rs543152725 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000747 | TCAAACTTTGTATGA[C/G]TGCTCCAAAATACCC | 9886 |
rs543196886 | in-del | -/TCG | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904253 | CACCTGGCCTATTTC[-/TCG]TCTTAAAGAATTTTT | 9886 |
rs543205003 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982799 | AAGTTACAGGGCTAG[A/C]ATGCATGTAGACTCT | 9886 |
rs543231933 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898026 | ATTATATTTACCCAA[C/G]TTCTGCTTGAAGTAT | 9886 |
rs543275316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885435 | GATGTAGCTGCTTCC[A/G]CTAGACCTAAGTACC | 9886 |
rs543301289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978049 | GTGAGGAAAAATGTA[C/T]AAAATTATTGCTAAG | 9886 |
rs543302638 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886692 | TACCAAAATGTAACC[A/G]AATTACTGTTTTTTT | 9886 |
rs543359161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993564 | TCTTCTAGCAAGAGT[A/G]TTGAATTTCATGGCA | 9886 |
rs543369668 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971871 | CAACCCCATCAAAAA[C/G]TGGGAAAAGGATATG | 9886 |
rs543446638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930906 | ACGAATCTTTCTTGG[A/G]ACCTGCCCTTTTTTA | 9886 |
rs543447434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922854 | TTTGACCCTATGATA[A/G]AACTGATTGATCTTC | 9886 |
rs543482949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923809 | AGAGTTTCTGCTTTC[A/G]CTTGGATCTCATTTT | 9886 |
rs543485650 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916839 | GATTATCCTGGACTA[A/T]CTATGTGGGTGCAAC | 9886 |
rs543509375 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941901 | CTACTGCCTGCCAGG[A/G]GTACATGGGGAGCCA | 9886 |
rs543545521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972540 | GGGCCTGTCGGGGCA[G/T]GGGGGGCTAGAAGAG | 9886 |
rs543546295 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939520 | CTGCCCACACACTCG[C/T]CCATCTCCTACCCTT | 9886 |
rs543547295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873014 | TCGCTCTTGATGTTT[C/T]TTTGGTCAGGTGGAT | 9886 |
rs543639579 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934819 | GAGAGCTGGTGAACG[C/T]GTATTGTAAAGAGCC | 9886 |
rs543698663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993722 | AGCCTTTTTCTGTAG[A/G]CCCTAAATCCTTTCC | 9886 |
rs543714608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905555 | AGTAACAGTGCCATA[C/T]TGTGTCTGAGGCAGA | 9886 |
rs543719172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936915 | AGTTCAGCCACTTCA[C/T]AGCACTGGGAAAGAC | 9886 |
rs543832169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933592 | GGGTGTGGTGGCACG[C/T]GCCTGTAGTCCAAGC | 9886 |
rs543853603 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940492 | ATCCAAATCCATCTA[C/T]GTGGTGCCTTTCAGA | 9886 |
rs543868094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933974 | ATACTAAAATATTAA[C/T]GCCAACAACTTTTTA | 9886 |
rs543926344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980695 | CTCTGGGGAATAAAG[A/G]AAAAGGAAAAACCTA | 9886 |
rs543956269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907163 | CTGTGAGTCCATTAA[A/C]CCTCTTTTTCTTTAT | 9886 |
rs543958004 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896018 | TATACAATCAAGTAA[C/T]TATTTTCAGAATGCC | 9886 |
rs544000060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976246 | GGATTTTTTAAAGGA[A/G]AAAATTTATGTACTT | 9886 |
rs544031631 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001160 | CTGGAAGCAAGCACC[C/T]TCTGGGGCCCTGTGC | 9886 |
rs544035233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936906 | CCTAGCCCCAGTTCA[A/G]CCACTTCATAGCACT | 9886 |
rs544037488 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962906 | TTAAAATATCTACCA[A/G]TTTCAATGTATGCCA | 9886 |
rs544056190 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944810 | GTGCTGGCTGGCTCC[A/T]CCACTCTGGGTTACC | 9886 |
rs544070161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994146 | AATTCAACGAATTGA[C/T]AAAATATTTGTTGAG | 9886 |
rs544077252 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892415 | TGTGTGTTTGTATGA[A/G]TCTGATGTTCTCTGG | 9886 |
rs544109993 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943818 | AGGCCCCCCTAGCGG[-/CT]CGGTCCCACAACTCT | 9886 |
rs544111746 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906620 | AACCGTGAAATGAGC[C/G]TATTTTGCAGGCTCA | 9886 |
rs544130050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947591 | GATTGACTTTTTTTG[G/T]TTGTTTGTTTTTTTA | 9886 |
rs544159185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997350 | CAGTTGTGTGGGTGC[A/C]ATCTCAAACCTATTA | 9886 |
rs544239040 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982545 | TGCATCTAGGGATAT[C/T]AGCAAGCATCCTTGG | 9886 |
rs544263255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927043 | GATATGAAATCAGTA[C/T]ACTAAAATAAGTAGC | 9886 |
rs544279397 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902325 | GCATGTAGTCTAACA[C/T]GTATCTGTTTGTTTT | 9886 |
rs544298423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920551 | CCATAGTCAGGAGTT[C/T]GGATCTTATTCTAAA | 9886 |
rs544312175 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926395 | TGAGACCAGTGTTAT[A/C]CTGATACCACAAGCA | 9886 |
rs544313101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983847 | GCCCCGCCCTCCTTC[C/T]GGCCTGTCCCTCTAC | 9886 |
rs544317699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985210 | AAGAGTGAAAATAAC[A/G]AATAATTTTATGGGT | 9886 |
rs544350679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898275 | CTTTGGGGCTTCAAG[C/G]TTCTTTTTCCCTGCT | 9886 |
rs544354875 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991842 | GTGCATCATTTGGAT[A/C]TCATTTTACAGAACC | 9886 |
rs544390222 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908134 | GAACATTGCAAATTC[A/C]AGTTGGCCAACTGCC | 9886 |
rs544409607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947102 | CAAGTAGTACAGACC[A/G]TATTTTGCTAATAGG | 9886 |
rs544426729 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877150 | AGTTCATATATCCTA[C/T]GCAGACCTGCTTCAG | 9886 |
rs544427831 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870335 | TAGGAGAACGCAGGC[A/G]CCCAGCCTCCAGCTT | 9886 |
rs544445271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970214 | AAAAAAATTGGTTAT[C/T]TGTGGTTACAAGTCT | 9886 |
rs544536443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990386 | TTGTCTACTCCCCAA[A/G]AATCTTTTTGAGACA | 9886 |
rs544536841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941235 | TTTAAAAAATCCTAT[C/T]TGTGCCATTTAATAG | 9886 |
rs544541041 | snp | C/T | 0.5 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971484 | TGTTGGGAAAACTGG[C/T]TAGCCATATGCAGAA | 9886 |
rs544553300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955298 | CGCCTGCTTCGGCCT[C/T]CCAAAGTGCTGGGAT | 9886 |
rs544571303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909016 | AAATGTTACAGACAA[A/G]GGAGCAGAACAATGC | 9886 |
rs544600083 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967366 | GGCCCTGTCTTGGCT[C/G]ACCGCAATCTCCACC | 9886 |
rs544603284 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871965 | ACAGGGCACCCTGGA[C/T]TCTAGCCCACCCAAC | 9886 |
rs544640109 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903076 | GGGAACATACGGAGA[C/G]ACACCTCACCTGGAT | 9886 |
rs544642325 | in-del | -/GA | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967835 | ATTTTATTGAAATGT[-/GA]GAGATTTGGTCATAT | 9886 |
rs544673686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928345 | CAAAAAAAAAAAGAA[A/T]ATCAGTATATCAAAG | 9886 |
rs544678025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921096 | TGGGATTACTGGCAC[A/C]CACCATCATGCCTGG | 9886 |
rs544687529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952044 | GCCTGGACAACAGAG[C/T]GAGACTCTGTCACAG | 9886 |
rs544705580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992531 | TTATATCTTAGCTTC[C/T]AAAATTTATGTCATC | 9886 |
rs544708858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890592 | CTTTATTGTGACACA[C/T]ATCACAAAGTATTGA | 9886 |
rs544724446 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950443 | GACCACCTGTTTCAT[-/A]TAACTTTCTCTTTAT | 9886 |
rs544726649 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903529 | AGCTACAAAAGACAA[A/C]ATTGTTACTATTTGA | 9886 |
rs544735541 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897715 | TACATATACATATAA[-/T]TTTTTTTTTGAGATG | 9886 |
rs544764918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998127 | TGTCCATTTGTCCTG[C/T]GTGTCTGAGGGCGGC | 9886 |
rs544811096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876496 | GAGATTGATCACAAA[C/T]CTTGTTGGGCAGATT | 9886 |
rs544842719 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883771 | TGAACTGCTTTGCAA[A/G]TAATGACTCTTACAC | 9886 |
rs544852217 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903571 | AAAATTTTCACAGAA[C/T]GTGGTGTTCTCTATT | 9886 |
rs544889074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998239 | TCATTTAGGCTTTCC[C/T]AAGGAAGGGACAATA | 9886 |
rs544908464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903019 | GCCAATTTTCCCGCA[A/G]TACAGTTATTGCTAC | 9886 |
rs544917170 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959128 | CATATGTTCAAGAGA[C/T]ACAAATAAGCAACTG | 9886 |
rs544983853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949960 | TAGGTTTACCTAAAG[A/T]CCTTTCTGTGTGGAT | 9886 |
rs544985879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942263 | TTAAAAGACCAAACA[A/G]TTTTGGCTTTTCCTG | 9886 |
rs545009370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983910 | AAGCTTCCCAGGTAG[A/G]ATAGCAATGAAAGAT | 9886 |
rs545029196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970234 | GTTACAAGTCTATTC[C/T]AATTTTGCTTATTAT | 9886 |
rs545035714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992749 | CTGCAATTATGAGAG[C/T]AAAAACATTCCACAT | 9886 |
rs545046536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884431 | GATGTTAAAAATACT[C/T]GCAAAACTCCACAAA | 9886 |
rs545098980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914712 | CTTTGAGAGTAACAG[C/G]AGCCCTTCTAGTTTT | 9886 |
rs545116385 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977085 | CATGGAAAGAAGGCA[C/T]GTTTCTAATTAAACA | 9886 |
rs545130052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978214 | TTTAATTTTTAATGG[C/T]GTCTTCAGAATTCTG | 9886 |
rs545131033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935977 | GTGCTTGCTTTATTG[C/T]TCTAGATCTAAGAAA | 9886 |
rs545166152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985690 | AATTGAACTAAAAAA[C/T]GAAATATTTCTATTT | 9886 |
rs545207302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940530 | AGGTTCCAGGAAAAA[G/T]CCAGTACTTTTAAAT | 9886 |
rs545234217 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946697 | AAAGTTCAGTGTCAT[A/G]CTTCTCTTAAATAAT | 9886 |
rs545239663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963140 | ACCACACCATTTGGT[A/T]TGACCAAAAGTTATG | 9886 |
rs545246017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933693 | GTGAGAGTGAGAATC[C/T]GTCAAAAAAGAAAAA | 9886 |
rs545254287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890271 | TTGGACTGGTGCATT[A/G]GCCCCTTAACTAATC | 9886 |
rs545266925 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945437 | TCCATCCTATTATAA[A/G]GGATGCTTCTTTGGC | 9886 |
rs545267694 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972948 | AACAAGTGCAGTGTC[A/G]AAAGCAAGAATGATT | 9886 |
rs545272173 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920596 | ACTGCAGTGTTTAAG[C/T]AGAAGTGTGGTAGGT | 9886 |
rs545278425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955940 | ATTGAACTACTATCA[C/T]GTGGTATTCTGCAAA | 9886 |
rs545307634 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998248 | CTTTCCCAAGGAAGG[A/G]ACAATATATTAGCCA | 9886 |
rs545321959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915240 | TCTAATTTATTCATA[A/T]CTAGCATTCTGATGG | 9886 |
rs545339163 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949365 | GGGCTGTCTTTGAAA[C/G]AATCTGTGTGTTCGT | 9886 |
rs545360661 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909120 | TGTTGTATTGTAAAA[C/T]GACTCCAGCTATGTC | 9886 |
rs545460237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904186 | ACCTGGCCTCAAGTG[A/T]TCCACCTGCCTCAGC | 9886 |
rs545489122 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986294 | GTCAAATGAGATAAT[A/G]TTTGGAAAGGAATTT | 9886 |
rs545510664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981799 | TTTAACACGGAGTTT[C/T]GCTTTTGTTGCCCAA | 9886 |
rs545521654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898925 | CACCAAACCCTAAGG[C/T]AGATAATATTGAAAG | 9886 |
rs545577427 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895630 | GCTGGTCTCAAACTC[C/T]CCACCTCGGGTGATC | 9886 |
rs545594353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989901 | GGAGAAACAGGTGGG[A/G]CTGTGCTCATACAAT | 9886 |
rs545597735 | snp | A/G | 1.72157e-05 | 0.00293386 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871445 | GTGGATCAGATTACC[A/G]ATTGGTTTCTGTTTT | 9886 |
rs545603491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872070 | CCACCAGCCAGTCTC[A/G]AGGAATCATCCATGA | 9886 |
rs545613280 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891149 | AACAGAAGGATTGTG[A/G]AAACTGAATATAAAG | 9886 |
rs545640091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878115 | AGGGAGTGGGCACAT[A/T]TTCAGGCTATGCTGC | 9886 |
rs545695329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903702 | TGGGTCAGACTATGA[A/G]CCACTGAGGCAGGGG | 9886 |
rs545703270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998971 | AGCCTCAGTTTTCTT[C/T]TCTGTGAAACACAGA | 9886 |
rs545704417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873990 | TTTTCCCCCTTTTGC[A/G]CCAGAGCAATCTCCT | 9886 |
rs545728550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956597 | AAATATCTTCTTTAT[A/T]TCCTTATTGTATAAG | 9886 |
rs545733401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959892 | GATTAAATACAATTA[C/T]GTAAATGGAGCACTT | 9886 |
rs545738316 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999623 | TAATTAATCCAAGTA[A/G]GTATACAGATTTTCT | 9886 |
rs545772840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906628 | AATGAGCCTATTTTG[C/T]AGGCTCACCACAAGA | 9886 |
rs545781869 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912209 | TGTGTGTGTGTATAT[A/T]TATGTGTATATATAT | 9886 |
rs545796579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912573 | ACAATAAAGCAAGAT[G/T]CAAAAAAATTATCTT | 9886 |
rs545802572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995141 | ATTATTTATGAGTAT[A/G]TCAAAGAAAATAATA | 9886 |
rs545806398 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946046 | GGCTGGGCGCGGTGG[C/T]GCACGCCTGTAGTCC | 9886 |
rs545815587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875758 | AAGTAACAAAAATGC[A/G]GTAGGAAGAGCCATT | 9886 |
rs545820550 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939086 | AACTCAGGTGCAGAG[C/T]GGAGACATGTAATTG | 9886 |
rs545822785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995751 | GCCCTTATTGTTTTT[C/T]GTTAATGCAATTTCA | 9886 |
rs545853358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894948 | GTTTTGAAATCAGAG[C/G]TAGCTTGGTTGTCAA | 9886 |
rs545861447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988994 | ACCTTGCTTTATTCA[C/G]ATTTCTAACTTCCAT | 9886 |
rs545882286 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961679 | CACCTAGGATTAGCA[A/T]GAAGTTCAAATGCAT | 9886 |
rs545886908 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962467 | ATAAAGTCGAAAGTA[C/T]TTATAAAGTCCAAAT | 9886 |
rs545913845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907701 | AGACATGGGGTCAAC[A/C]AGATGACCTTTTGAA | 9886 |
rs545923988 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960286 | CATAGAATTTCCATA[G/T]AATGTAATTAATGTG | 9886 |
rs545946888 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982484 | TCTCAACCTTGATAC[A/C]ATTGATTTTGTTGGC | 9886 |
rs545947510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974057 | ATCAGAATTTTCTAT[C/T]TCCATAACATGAAAT | 9886 |
rs545965035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874597 | ACAGGGGAGGCACTA[C/T]GGGGCTTCATGGAAT | 9886 |
rs545978680 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938677 | TAACTTCTATACTCC[A/G]ACATCTGCAAGAGTA | 9886 |
rs545983992 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882044 | TCATGGCTGATTTTT[A/T]AAAAAAGCCCGTTTC | 9886 |
rs546024497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918117 | AAGTGTTTGTGGGGC[A/G]TAGCTATTTGCTACA | 9886 |
rs546044472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881195 | CTTTTGTCTTCCACC[A/G]TGATTGTGAGGCCTC | 9886 |
rs546047182 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882664 | CAGATTTTCTCAAGA[C/T]AATAGAAAGTTAAAA | 9886 |
rs546061198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911883 | CTGGCACACATTTAT[A/T]GCCTACTGGATACTC | 9886 |
rs546107025 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002741 | GTAAAATTGGTTTTG[C/T]CTTGGAGTTTATGCA | 9886 |
rs546121368 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003281 | TTTTTATGGCTGTAT[A/G]GTATTCCATGGTGTA | 9886 |
rs546147024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961104 | GGGTGTGGGGCTGTC[A/G]TTCTCAAAGGACCCT | 9886 |
rs546163485 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870446 | CCCTGGGAAGAGTTA[A/G]AAATATGGGTCTTAC | 9886 |
rs546227071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953694 | GAATAGTCTAGTGTC[A/G]TAACAGTATCTTGTT | 9886 |
rs546239821 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981841 | ATGGTGCGACCTCGG[C/G]TCACTGCAACCTCTG | 9886 |
rs546241341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879372 | GTTTTTTTGAGACAG[A/G]GTCTAACTCTGTTGC | 9886 |
rs546273840 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974184 | CTTTCCAGCAGTTTC[A/G]AATACATATATTTAA | 9886 |
rs546278607 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877716 | CCCACCACAGAGTGG[A/G]TGCTTAAGAAATATA | 9886 |
rs546280215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906436 | GTAAGATTCAGAATG[C/T]ACCAGGAGGAAATTT | 9886 |
rs546289954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966969 | GCACGACAAAGTTCT[G/T]GGGGAGAAATATTAT | 9886 |
rs546312463 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001755 | CGCGTGGGGCTCCTA[C/T]TGGGACCCCGGTCTT | 9886 |
rs546324702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967682 | GGTAAGAGGACACTT[C/T]GCATTCTAAATGCCT | 9886 |
rs546342466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925558 | CTAAACCCAAAATTA[G/T]TAGAAGAATTAATAA | 9886 |
rs546364429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954431 | AGCACTGAATGAATT[A/C]TTTCCATGTTCTTTT | 9886 |
rs546369675 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945151 | AAAGCAAACAACCGG[A/G]TGCCTGCCATCAGGG | 9886 |
rs546406796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937844 | TAAAAGACTTTCTTT[C/T]GAGATACTCTAGGAA | 9886 |
rs546419409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932200 | CTTTACTTAGGCAGA[C/T]GTCTACACATTTTCA | 9886 |
rs546422586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901372 | AAAGTGTTCTGTAAC[C/T]GTTAAGTGCCAATTA | 9886 |
rs546445541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938324 | GACTTGGCACTTTTC[A/G]GGCAGTGTTATGTAA | 9886 |
rs546461566 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933476 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 9886 |
rs546481035 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927816 | TGGACAAAGATTTCC[A/T]GAGATCTCACAGCAA | 9886 |
rs546503239 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983975 | TTTTTATCACTTACG[C/T]ACTTTAATTCCCAAC | 9886 |
rs546508099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968361 | AAATGAATTTTGTTT[A/C]CAGACATATGTAATT | 9886 |
rs546524329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987818 | CATTCTAAACCATCT[C/T]CCCTCACTATCAAAT | 9886 |
rs546567808 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931689 | GATAACACATAAATT[A/G]TTTTTTCAAAACTAT | 9886 |
rs546614720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887654 | AAAGGAGAGGGGATG[A/G]AAACAGATGAGACAC | 9886 |
rs546623945 | snp | C/T | 3.4323e-05 | 0.0041425 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871447 | GGATCAGATTACCGA[C/T]TGGTTTCTGTTTTTT | 9886 |
rs546661534 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949265 | AGCCTTCCATCTAGG[A/G]TCCCTTCCCCAGCTT | 9886 |
rs546662223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889841 | TTATTAGCATGGCAA[C/T]GCTAAGCATAGTATT | 9886 |
rs546666063 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912690 | AGAAGGTTTAAACAG[A/G]GCTGCTGATGAGAGG | 9886 |
rs546672450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990547 | GACCAGTATTCTCCA[C/T]CCGTGCTCAATAAAA | 9886 |
rs546677740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881580 | GCTGTGTGACCTTTG[A/G]TACATCTCTCACCCT | 9886 |
rs546681190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918676 | GCTGTGAATCATCCC[A/G]CCATTGGAATATGCT | 9886 |
rs546681311 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956329 | GCAGGACTGGAAGTT[C/G]TTCTGGGTGAGTCAG | 9886 |
rs546700730 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916376 | CAGCTCAGCCAATCC[C/T]ACAGCTGAATGTAGT | 9886 |
rs546700982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896404 | GACCTCAGGGGTCCT[A/G]TTTCAGCTGTAAAAG | 9886 |
rs546727634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929878 | AAATTAATAAATATC[C/T]CACATTTTTTAAACC | 9886 |
rs546768452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900080 | GGACCATGCCATTCT[C/G]CTGGAGCACAGTCGT | 9886 |
rs546775269 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974154 | CTATAATCAGTTAAG[A/G]GTGTTGTCACCCCTC | 9886 |
rs546784208 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869838 | CCTTCTCTTTTGTCA[A/T]GACAAGGTGATGCAT | 9886 |
rs546801897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983295 | AGACTATTGGTATTA[C/T]ACTTTACATAGATCA | 9886 |
rs546813364 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875621 | AAGAGGTTGAGTGAC[A/G]GAGGAATGAGTCTAT | 9886 |
rs546820933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875335 | AACTCCTGGCCACAC[A/G]AGACTATTTAAACTT | 9886 |
rs546856768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988517 | TATGTCCATGTGTAC[A/C]CAACATTTAGCTCCC | 9886 |
rs546862416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995286 | CCTTTGAGGAAGGGA[C/T]GTTACTACTTTTATT | 9886 |
rs546892819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997019 | CATTTTTGAACATGC[C/T]TGATTTGAGCCAATA | 9886 |
rs546939818 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904550 | TTTTGCTTGGCGTCC[C/G]TTACTCAAAAGCTCT | 9886 |
rs546990383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907341 | TTATAAGAGCTCCAG[G/T]AGACAACTCTTGAGT | 9886 |
rs547018751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953903 | AGGGACTGAGATATT[A/G]GGAGATGGTAAAATG | 9886 |
rs547030562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939890 | GATTATTATTAGAGA[A/T]GCCATGCTAATTCCT | 9886 |
rs547069157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899389 | GAATGACTGAGGAAC[C/T]TCCTTCCTCTACTTT | 9886 |
rs547071491 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993778 | TTATAGGTAGTCTTT[A/T]TTTTTTCCTCTGGAG | 9886 |
rs547105957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899087 | AATGAAATCAGGCCA[C/T]TTTCCACTCAAAATC | 9886 |
rs547131287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936558 | GCAAATAAAATAAGG[C/T]GGTCTGGTTATGGCC | 9886 |
rs547144241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960357 | CAAATAGTATGTTTA[C/T]GTAAGTAACACAACA | 9886 |
rs547174556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953029 | TCCACTTCCTGATGA[A/C]ACAAGCAGGATACTA | 9886 |
rs547177661 | snp | A/G | 8.2479e-05 | 0.00642127 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872303 | AAACTGCAGAAAAGT[A/G]AGCAAAAGGAGGGTA | 9886 |
rs547214679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878359 | ATTAGGGGCCCTCAT[A/G]CCAAGCACCTTATAA | 9886 |
rs547239252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872649 | GCAGCGATGTCATCT[C/T]TGTTTAAGGAAGCCT | 9886 |
rs547253025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912954 | GTTAAACTGAGAAAA[A/G]TGGGTGGGCGGTCAT | 9886 |
rs547278793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903975 | CTTTTCTTTTCTTTT[C/T]TTTTTGAGACAGGGT | 9886 |
rs547291452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913509 | TTCTATGGTTTTCTT[A/G]GTTACCCATCTAACA | 9886 |
rs547348836 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909869 | GTGTGTGAAATAATT[A/C]CTGGGAATAGGGCAA | 9886 |
rs547394622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950123 | CATGCATAAGAGGAG[A/G]TAGCAAACAGTTTTT | 9886 |
rs547415122 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987816 | GACATTCTAAACCAT[A/C]TCCCCTCACTATCAA | 9886 |
rs547431341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943435 | TCTGCAAGCCCCTCA[C/T]GGCAGCTCCTCCTGT | 9886 |
rs547469518 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944115 | CCGCCCGCCGCCCAA[C/G]TTTGCACAAAGGCAG | 9886 |
rs547511615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911056 | CAGGAGAAGCGTGTT[C/T]AAGTCAGCACCCTCA | 9886 |
rs547539079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978565 | GCAGTGTAAACCCGT[A/G]CTGGGACAGTAGCAT | 9886 |
rs547560056 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981054 | ATTTCCTTAAAAATA[C/T]CCTTACTGGGAAATT | 9886 |
rs547560306 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959068 | CAAAGTTGCCTCAAC[A/G]TTCAAAAATCAGTCA | 9886 |
rs547649358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923291 | ACAGCAGAAAAAAAC[C/T]TCAAACATCTGATTC | 9886 |
rs547657887 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966519 | TAATTAAAAAAAAAA[A/C]AAGTTGGAAACTATA | 9886 |
rs547665625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929796 | AAAAAATCAGAATAA[A/G]CCAATGTCAGATTAA | 9886 |
rs547681909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910262 | AAGGCACTTTGACCA[C/T]GTTCCTACCCATATT | 9886 |
rs547689365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916287 | GGATGAGAATTCACA[C/T]TGAAAACCGCTGAGG | 9886 |
rs547691366 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974388 | AATAACTATAGTTTC[A/T]CTTTGTTTTTCAAAT | 9886 |
rs547819348 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961280 | GAGATGACACAGTAT[C/G]CCTAGAGCTGGACAC | 9886 |
rs547856598 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893635 | TAACATATAACTAGG[C/T]GAGAATTAGATTGAT | 9886 |
rs547856659 | snp | A/C/G | 3.29648e-05 | 0.00405974 | missense, synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886169 | TGCCATCCACTCACA[A/C/G]CTACAGATCAGCAGC | 9886 |
rs547891822 | snp | A/T | 1.68695e-05 | 0.00290422 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893001 | AACATCAGACCTAAA[A/T]GGAAATCATAAAAGA | 9886 |
rs547895636 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929468 | TTAAGGAAACTGCTC[A/C]AAGATACTAGCGAAA | 9886 |
rs547911215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951827 | TTTGGGAGGCCAAGG[C/T]GGGCAGATTGCCTGA | 9886 |
rs547930839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930393 | CATCAGTAAGTCTTA[C/T]CTATTAATATTGTCA | 9886 |
rs547963029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936936 | TGGGAAAGACATATA[C/T]TTGCTACTTCTAAAT | 9886 |
rs547985930 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957459 | TGTTCACAGTTGACT[-/G]GAAATGTCATTATAT | 9886 |
rs547990109 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900027 | ACAGAGCAAAGGCCC[A/G]AGGTAGGAGCCTGCC | 9886 |
rs547993491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957552 | CACCACCAAGCCTTA[C/T]GGTCAATACAAATTC | 9886 |
rs547994187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972307 | GCCCATCATGATAGA[C/T]TGGATAAAGAAAATG | 9886 |
rs548001702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872690 | ATACTTCGTGTCGCA[C/T]GTCAGAGCTCAGCTT | 9886 |
rs548018886 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975240 | GAATCAGGGGAATTC[A/G]TCAGAATGTGTAAAT | 9886 |
rs548050496 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913219 | AACTGTCGACTGTAA[C/T]GCCATCACAGGAGGT | 9886 |
rs548052330 | snp | G/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885665 | AAGGTCCCCTGTCTG[G/T]TTAGGGGCATAGCTA | 9886 |
rs548075817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873169 | ACAGTTTTAGCTGGT[A/G]CTTCCAACTTCTCTT | 9886 |
rs548078444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879777 | ATGATTGCACCTCTC[G/T]CTCCATACACATGCA | 9886 |
rs548080933 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906725 | TGTAGTTGTTATCAC[G/T]GTCAGCAACATAGGC | 9886 |
rs548083918 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937852 | TTTCTTTCGAGATAC[C/T]CTAGGAAGGCTAAGA | 9886 |
rs548085055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993859 | GAGCATTAAAATTTA[A/T]AATTCTTTTGTAGTA | 9886 |
rs548112190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999862 | GTAAGGTAAATGCCA[C/T]TTCATATACAGCTTT | 9886 |
rs548132033 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898860 | AAAGTGGGGCCAAAG[C/G]AATGCATGCTCTTAA | 9886 |
rs548144990 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965175 | TAGAGAAGACAAATA[G/T]TATAGCAGCATATTT | 9886 |
rs548146068 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944217 | TCGCCCCTTTCCACC[C/T]GCAGCCCTCCCCTTC | 9886 |
rs548174938 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870550 | TGGCAGGAGGGAGTC[C/G]AGGGACCTTTTCCCT | 9886 |
rs548193571 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878397 | CTGTGGGGAAAGAAA[C/T]CTCCTAGCAACATGA | 9886 |
rs548209779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904784 | TTTAACCTAACCTCT[C/T]AGGGAACAACTATTT | 9886 |
rs548219021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912140 | AAGTCTAAATTTAAT[C/T]AAATTAACTTATATT | 9886 |
rs548262507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951917 | CAAAAAATTAGCCGG[A/G]CATGCTGGCAGGCAC | 9886 |
rs548280280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980174 | TAATAGTTCAACTCT[C/G]CGCTTTGCATTAGCT | 9886 |
rs548280687 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955969 | AAAATATCACAGTGG[A/G]CCTCATTTGTTAATA | 9886 |
rs548394515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996140 | AGGCTGATTGACTCT[A/G]GAGCTTGGGCTTCCT | 9886 |
rs548432571 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000938 | TGCAGATGCTGCGCC[C/T]ACTTTCAGAAGACCC | 9886 |
rs548443956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952931 | CACAACCACAAATTC[A/G]AAGAAAACACAATTT | 9886 |
rs548480979 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910897 | TTTACCTGCCATATG[C/T]AAAGCGTCTGTCTTT | 9886 |
rs548531330 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879836 | GGCACACACATGCAT[A/C/G]GAGCCAGCCATCTCT | 9886 |
rs548550908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943642 | GAAGCGCCTTCTCGT[C/T]GGCGCGGCACCACCC | 9886 |
rs548566703 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959440 | ATCACTTTAAAAGCT[A/C]CGTGGACAAGAAAGG | 9886 |
rs548573455 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876866 | ATTTTTTCTAAAGAC[A/G]TTGCCAGAAAGTCAA | 9886 |
rs548576089 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952231 | TTATCTGTTCTACTG[C/T]GATCACTGTCAACAC | 9886 |
rs548591624 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973330 | TAGGAGATCATCAGG[A/G]GGTCATTTAGTTTAT | 9886 |
rs548592472 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002817 | TTAATGAATTCTTTC[C/T]TTTTCAATATCTCTA | 9886 |
rs548606226 | snp | C/T | 0.00119952 | 0.0244606 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918386 | TCTGTCCCTCTCTTA[C/T]GAAAGAGACTCCCAG | 9886 |
rs548608663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914832 | AAGGTGAGAATAACA[C/T]CTATGGGTCCTCTAA | 9886 |
rs548625611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995427 | TTTCCAAAATTAGTG[A/G]TCAGCCTTATTACCT | 9886 |
rs548653694 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971345 | CTGGTACCAAAACAG[A/T]TATATAGACCAATGG | 9886 |
rs548658874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998506 | TTTGTAATCGGCTCC[A/G]TGAGGGATAACTGAG | 9886 |
rs548693866 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910558 | AACTTAAAACATTCT[A/C]ACAGAAGGCAAGTGA | 9886 |
rs548701735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988573 | TTGGTTTACCAGTTC[C/T]GTGATAATTCCCTTA | 9886 |
rs548702976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955440 | AATAACAAAAAAATG[C/T]TGTACAGACATGGAT | 9886 |
rs548707591 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900419 | AAGAGTTCAGAATAA[C/T]GATAAGCTTTTTCGT | 9886 |
rs548758276 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880532 | TCAGACATGGTTGGT[A/G]AAAACGACAATTATG | 9886 |
rs548790751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931167 | GCACGTCTTATTTTT[C/T]TAAAAAAATGTGAGA | 9886 |
rs548793548 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924125 | TTTTTTTTCAGTAAA[A/T]TGTTTACATATCAAT | 9886 |
rs548804748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890328 | TAGTCCACAGTCCTC[A/G]CTGCTGCAAGAAAAG | 9886 |
rs548829296 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920659 | GTTTTGTTTTGTTTT[G/T]TTTTGTTTTGAGTCA | 9886 |
rs548830146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917699 | TCTTAATACAATCAC[A/G]TTGGGGGTTAGGGCT | 9886 |
rs548842942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948854 | ACATATTTATACTGC[C/T]CATGCTTATGGATTT | 9886 |
rs548868096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914207 | GGGTGTGGAGGGGGC[A/C]GGGAGGAGGTCACAG | 9886 |
rs548890351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965847 | GACATCTGATAGGAC[A/G]TTGTCTTGCCTTGTT | 9886 |
rs548898330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933734 | GTTCATCATCATATC[A/G]CTATTTGTGGAAACA | 9886 |
rs548899632 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897719 | TATACATATAATTTT[G/T]TTTTTGAGATGGAGT | 9886 |
rs548915824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971149 | CATCTGATACATGAG[G/T]TCTATTTTTTCACTT | 9886 |
rs548922624 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885905 | AAACAATAGCTCCTC[-/A]AAACTGCAGATCTAA | 9886 |
rs548925314 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966839 | CTATCCCTCCCCCCT[A/C]CCCCCACCCCACAAC | 9886 |
rs548931056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927252 | ATAGATGGGAAGATC[A/G]ATATTGTTACAATGC | 9886 |
rs548990779 | snp | A/G | 0.00020495 | 0.0101209 | missense, nc-transcript-variant, synonymous-codon | RHOBTB1 | GRCh38.p7 | 10:60871631 | GGGGCCAGCGGTGCC[A/G]CTCGAAGTATTCCTG | 9886 |
rs548991927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877454 | TACAGGACAAAGTCA[C/T]CTGGTCAGTAAATGG | 9886 |
rs549002225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908132 | AGGAACATTGCAAAT[G/T]CAAGTTGGCCAACTG | 9886 |
rs549009512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916136 | GCTTCTGACTGCTTC[A/G]CCCAAAAGAATGTGG | 9886 |
rs549010499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883532 | ATAGCAGGTCCTCTG[C/G]TGCACAATCAGCATG | 9886 |
rs549020793 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948766 | AGTTGTTGGAGTAGA[C/T]TCTTGCAGTTAAGCC | 9886 |
rs549025922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872358 | CAAAGAAATTGGGGA[A/G]GCCATTTTAAGGGTG | 9886 |
rs549029463 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871245 | CTAACAAAAAAAATA[C/T]ACATATCAGTTTAAG | 9886 |
rs549050960 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969679 | TGTGTTTTAGCATCA[A/C]TTCAGTTGTCAGAAG | 9886 |
rs549054645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963540 | TAGAAAAATGCATAT[C/T]CAGGCTCTCCCTTTG | 9886 |
rs549068330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998384 | AAAAAAGTCAGAAAA[C/G]AGAGTTCTGGCCTAT | 9886 |
rs549100288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928754 | ACAATAATTTATTGT[A/G]TAGTTAAAAATAACT | 9886 |
rs549120660 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930173 | TATTTACCACATCTT[C/T]AAGAAAAAAAATGAA | 9886 |
rs549139164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922093 | TAAATGTTAATAATA[C/T]TTATATATAAGGGTC | 9886 |
rs549142762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941686 | TGAGTCCATAAAAAA[G/T]TCAAAGACAAAATTT | 9886 |
rs549144873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885115 | GTTCTATTGCACAGT[A/G]TGGTGACTATGGTGG | 9886 |
rs549155578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926628 | GAATGAAGGAAAAAA[A/G]CAATATGATCATTTC | 9886 |
rs549202860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898771 | GATTAGCTTGTGCAA[C/T]TATTTTTTTCCAAGC | 9886 |
rs549216166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935231 | AAGCCAGGCACAAAA[G/T]AATACATAGGATATG | 9886 |
rs549226722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966422 | CCCCTGTAATCCCAG[C/T]GCTTTGGGAGGCCAA | 9886 |
rs549271328 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918870 | TCCTGACTCAGCCTC[C/T]CGAGTAGCTGGGATT | 9886 |
rs549273947 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948668 | GACTAGTACTAACAG[C/G]GGTTTGAAGCACGAA | 9886 |
rs549275014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922533 | ACCACTGATGACCAG[C/T]AGACTGCCATGTCCA | 9886 |
rs549297305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969786 | GCATTTATTACATCA[C/T]AATATGACTTAGCTT | 9886 |
rs549312814 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992946 | TCAAAGAAAGAAATC[A/G]TAGAAGTCCCAGATA | 9886 |
rs549334302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961909 | CGCTCCTGGGTTCAA[A/G]TGATTCTCCTGCTCC | 9886 |
rs549334367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970431 | ATGCATTTTTCCTTT[C/T]TAGTTCCTTAGATCA | 9886 |
rs549356115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885641 | TGAGGCACAGGAATG[C/T]GGCTTCTCAAGGTCC | 9886 |
rs549388370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985303 | GGGAAAAAACTCAAT[A/G]ATGTGGACCTTTTTT | 9886 |
rs549409907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909501 | AAAAAGTCCTTTGAA[A/G]TCTACTGTATTTATC | 9886 |
rs549427099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977631 | CTGTAAATCTCAATA[C/T]ATCTTTTCTGTCCCA | 9886 |
rs549431658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947233 | TAAAATCATTGCTTG[C/T]TGATAGAATCAGTAC | 9886 |
rs549483484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903860 | GATTTACGTTTTCAA[C/T]GAGACTAACTTAAAG | 9886 |
rs549502874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916415 | GAGCCCAGGTGAAAC[C/T]AGCAGTGGAATCACC | 9886 |
rs549539156 | snp | A/G | 4.94605e-05 | 0.0049727 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888409 | TCATCCAGTTGTCCC[A/G]TATAAAGAAACTGGA | 9886 |
rs549591983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898582 | AGGATGGAGAGGCCT[C/G]TAGGGGAGCGCCTGG | 9886 |
rs549593070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984402 | GCATATGACTATTCT[A/G]AATGTTCCTTTAAAA | 9886 |
rs549597635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884074 | ATAACTCTAATATTT[A/T]TTCCCTGAAAAGCAG | 9886 |
rs549601614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903815 | TTCAGCTATTAAGGA[C/T]CTGGTTCCATTTTTT | 9886 |
rs549639798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992173 | TCAGTCACAAGAGCA[C/T]TGAAAGCCTTGAATG | 9886 |
rs549655540 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976281 | TATTTAATTTGTACT[C/T]GAATATTTGAAATGC | 9886 |
rs549663786 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991300 | CCTCAATCTTCTCAC[G/T]GGTCCTAGGATAAAG | 9886 |
rs549670411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891810 | GGTTTGGCTATGTCC[C/T]CACTCAAATCTCATC | 9886 |
rs549671547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908799 | GGTCTGTGTCAGGAC[A/G]CCTGGAGGCTGTGAG | 9886 |
rs549708723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877640 | CAGCATGCATACAGC[A/G]TGTGCCTCAAGGGCA | 9886 |
rs549711060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891232 | AGAAAGTACCATTTA[C/T]TATTGCTTGGAGAGC | 9886 |
rs549711118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898496 | AGTGTGTATGAGATG[A/C]AGAGGGAGTTGTCAG | 9886 |
rs549768712 | snp | C/T | 2.20378e-05 | 0.0033194 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871692 | AAGACCTGCGGTTCA[C/T]TGATGCCTTTTATGT | 9886 |
rs549775467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956137 | GGCTATATGGTATAG[A/C]CCGTTGTTTCTAGGC | 9886 |
rs549812024 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884963 | TCACTCTGTCTCCTG[A/G]GGTGGAGTACAGTGG | 9886 |
rs549821023 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955551 | ATCCCAAACCACAGA[-/G]AGTTGCTAGCTATCA | 9886 |
rs549850570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992991 | GAAACTAAGGTTAGC[A/T]GGAATAACTTGCTTT | 9886 |
rs549892661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957645 | GCTAAAAAGCAGATC[C/T]AAGTGAGTAAGTAGT | 9886 |
rs549905462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872788 | CATAAGAAGAGCAGG[C/T]GGTATGGGCAGGGTG | 9886 |
rs549924662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985351 | CACTTGGGATGACTC[C/T]AGTTCTAATAAGATT | 9886 |
rs549940341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916718 | AGCCTCCCTGAATAC[A/G]TCCACGGAATCCGCG | 9886 |
rs549949608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950050 | TTCTGCAACTCTAAC[A/T]GCAGTCTTTCTGTCA | 9886 |
rs549954943 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989526 | GCTAATCTCTCACTT[C/T]CTCTTCATAGGCAAA | 9886 |
rs549997723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928019 | ATGGCAAAGGAACTG[C/T]ATAGATATTTCTCAG | 9886 |
rs550011252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878252 | TTGTAGTTGACAAAA[A/G]AGTGGAGCTGCCTGA | 9886 |
rs550019552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921901 | CCCTAACAGGAAGTG[C/T]ATCAGTAACCATGGG | 9886 |
rs550039697 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990036 | CGCCTAGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 9886 |
rs550041677 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970942 | CCCAGAATATATGCA[A/T]AACTCACCATTTTTA | 9886 |
rs550102982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972143 | TGGCGATTCCTCAAG[A/G]ATCTAAAACCAGAAA | 9886 |
rs550151637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933101 | TTAGACCATAAATGC[A/T]AAAGTGCTGGTGGAA | 9886 |
rs550202703 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928774 | TAAAAATAACTAAGA[A/G]TGAAATTGGAATGTT | 9886 |
rs550219854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916950 | TGGCTTTGAAGATGA[A/C]GGAAGGGGCTGCAAG | 9886 |
rs550232380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886031 | GGATTAAAGTCATCT[A/G]GCTGTTTACCCACTT | 9886 |
rs550239883 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953645 | TTTACACTGTAATTA[C/T]AGTATACAGTATACT | 9886 |
rs550242147 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965113 | TGCCATTACTTATCA[C/G]ATAGTATGTTAGGGG | 9886 |
rs550329387 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923949 | TATCTTTATCAGCCA[A/T]GTGAAAATGGATTAA | 9886 |
rs550333725 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956592 | TACAAAAATATCTTC[-/T]TTATATCCTTATTGT | 9886 |
rs550334622 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926262 | ATAAATAAATATGGA[A/C]AAGACCTGATGGCTT | 9886 |
rs550335341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943160 | TGCTAACGTGCAAAG[C/T]GAAGTCAAAACCCTG | 9886 |
rs550345890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938424 | GAGTAGTCAAGTTAC[A/G]TTGTTTCTCTGGGTG | 9886 |
rs550384668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938976 | ACAGTTGGGTACCAA[C/T]TCAAAGGAAATTTCT | 9886 |
rs550394584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899026 | TCATAGTACAAATAT[C/T]ATAGGGGTTAATGGC | 9886 |
rs550467924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885653 | ATGCGGCTTCTCAAG[A/G]TCCCCTGTCTGGTTA | 9886 |
rs550503574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967839 | TTATTGAAATGTGAG[A/T]TTTGGTCATATTACC | 9886 |
rs550546389 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925624 | ATAGAAAAAATCAAC[A/G]AAATGAATTTTTTTG | 9886 |
rs550565761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876282 | ACTATAAAGGATTAA[A/G]GGAATCATCTTGGGA | 9886 |
rs550594848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882797 | TACTTTCCTAGTTCA[G/T]AAAGGGAACTGGGGG | 9886 |
rs550603818 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983502 | GTGTCATGCTTATCC[A/T]GATTTTAGGATATCA | 9886 |
rs550604340 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902917 | AAGACACCAGGCCAC[A/G]TATCGGGGATAGAAA | 9886 |
rs550608817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895426 | ATTTATTTTTTGAGA[C/T]GGAGTTTTGCTCTTG | 9886 |
rs550627817 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882166 | AATGGAATCAAAAAA[A/T]TTCTATCCTACCTGC | 9886 |
rs550630543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890745 | ATTTGACGACTTAGA[G/T]GAAAAGGAGGGAAAA | 9886 |
rs550630800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883620 | GATTGCTGAAGTCAG[C/T]CAAATACCAACTGGA | 9886 |
rs550632146 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889491 | TATTTTCCAATTGTT[A/C]ATTTCTTAGTTTATA | 9886 |
rs550699761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913650 | TGAGGAGGGAGTTCT[C/G]CTTCTAGTGGGTAGA | 9886 |
rs550716939 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969248 | AGATACAGGGTGCGG[C/T]ACATATGACTTGGCT | 9886 |
rs550742391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897184 | CAAAATACCACACAT[A/G]TTCTCAGAGACTGTC | 9886 |
rs550798556 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894660 | CTCTGCTATAAGCTT[C/T]ATCCTGAACACAAAA | 9886 |
rs550814130 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976498 | GTACAGCCCCGTCTT[G/T]TTCCTTTTATAGCCA | 9886 |
rs550833226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989457 | CATATAAGATACGTT[C/G]ATACTTGTTGAATGA | 9886 |
rs550837300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981374 | CAATTCTCTCAAGAG[C/T]CCTACAAGGTAAATT | 9886 |
rs550903786 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906593 | TTGGCCCTTTTTTGT[A/G]CCTGTTTCTCCAACC | 9886 |
rs550906921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982767 | GACTTATGTAAAATG[C/T]CTTTCTCACACATAG | 9886 |
rs550957276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997822 | TCTGGGCAACCTAAG[C/G]CTCTTTTGAATTTCT | 9886 |
rs550974964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941515 | ATCAAGCATCCAGAT[C/T]CCCAGTATTCTCAAC | 9886 |
rs550998650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920591 | AAGCCACTGCAGTGT[C/T]TAAGCAGAAGTGTGG | 9886 |
rs551036911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947966 | TCCACATCCTCACTA[A/G]CATTTGTATTATCAT | 9886 |
rs551046875 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996198 | TTGATCATGTTCTCC[A/C]CACTTACATATCAAT | 9886 |
rs551052208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927344 | ACCCTTACAGACACA[C/T]CCAGGATCAACACTT | 9886 |
rs551059331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969701 | TGTCAGAAGAGTTTA[C/G]GATCATCATCTATGA | 9886 |
rs551062906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897888 | TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA | 9886 |
rs551082278 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885404 | CTTCTAGAGATAGAG[C/T]CAGGGGCTGACAAGT | 9886 |
rs551095373 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880525 | CCCACTTTCAGACAT[C/G]GTTGGTGAAAACGAC | 9886 |
rs551104551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954875 | TAAATGGTCAAGTTT[C/T]GGAAATAGTTCATAT | 9886 |
rs551136423 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871098 | TAAAGTAATACACAG[C/T]ATTTTCATTTCAACA | 9886 |
rs551182025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997195 | AAACACACTGAGTTC[C/T]TCCCGAAATATCTTT | 9886 |
rs551198231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908030 | GCTTTTGAAAAATTG[A/G]AGCTTTTATTCTAAT | 9886 |
rs551227345 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927947 | CTGACAAGGGATTAA[C/T]AACCAGAATATATGA | 9886 |
rs551276230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902060 | AAGGACAATTTCATC[C/T]TGGGGACAAGGCTGG | 9886 |
rs551286657 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999012 | CTCACCAGATTATTA[C/T]AAGAATTTAATGAGA | 9886 |
rs551301576 | in-del | -/GATTTGGGTGGG | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929175 | TATAATTGGATATGA[-/GATTTGGGTGGG]GACACAGAACTAAAC | 9886 |
rs551306850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933284 | GCAGGATGAAGCACT[A/G]TTTGTGGAAGTGGAA | 9886 |
rs551328723 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956056 | TCCTTAGGCAATTTC[A/G]TCGTTGTGCAAACAT | 9886 |
rs551351043 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966996 | TTATAAATAAACAAG[C/G]CACATCTTTAATTCC | 9886 |
rs551391079 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913792 | TTTGAATCCTAGCTC[C/T]CCCATTTTCCAGTCA | 9886 |
rs551424372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877712 | AGGGCCCACCACAGA[A/G]TGGGTGCTTAAGAAA | 9886 |
rs551424800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883451 | TTAGCATTCGTGAGG[G/T]CAGCTCTGACAGTGT | 9886 |
rs551444776 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963951 | TTTCCAACTGAAGGG[-/A]AAAAAACCTTGATTT | 9886 |
rs551476222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934469 | AGGAACAAGACCATG[A/G]GAAAACATTCTCTAA | 9886 |
rs551479643 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961956 | GGGATTATAGGCATG[C/T]ACTACCACGCCTGGA | 9886 |
rs551536301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932576 | TTTTGGAGGCCCTAT[C/T]GTCCTCATGGGGGTG | 9886 |
rs551668903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60882992 | TTTGACAAAGGTTTT[C/T]TTGTTATCCCCATTT | 9886 |
rs551718678 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969204 | CTATGGAGGTCCAAA[A/G]CAAACAAAAAACCTA | 9886 |
rs551734731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975619 | TTCAGTAACATTCTC[C/G]ACGTGCTGTTCTGAA | 9886 |
rs551741128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953467 | TCCTAGGAAACAAAA[A/G]GTAGTACCTAAGCGA | 9886 |
rs551756804 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915866 | GTGCAGCCCACATCC[C/T]AGTCTCACCATTTCT | 9886 |
rs551769122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991412 | TCTGCACTCCAGACA[A/G]TGTGGCCTTCCCTCA | 9886 |
rs551786668 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881071 | GGGTGGTTCCCCCCA[A/G]ACTATTCTAGTGATA | 9886 |
rs551797131 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940662 | ATACTGCAATTTAGC[G/T]GTTCTGGATGACTAC | 9886 |
rs551804093 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971398 | TAATGCCACACATCT[A/G]CAACCATCTGATCTT | 9886 |
rs551820903 | snp | A/C | 0 | 0 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928119 | GTGAAAACTACAATA[A/C]GATATAATCTCACCG | 9886 |
rs551837367 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990128 | GCTGGGACTACAGGC[A/G/T]CCCGCCACCACGCCT | 9886 |
rs551858790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891723 | AACATTAAAAAAACA[C/T]AAAAAGTTGTTTTTT | 9886 |
rs551920665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958445 | TTTTTATTTGAAGAG[C/T]AGGAATAAATGGATC | 9886 |
rs551922938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950994 | ACAAGTTAGCTAAAC[C/T]ACATGCAGAAACTAG | 9886 |
rs551957968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902868 | ACATGAGAGATTTGT[A/C]AACTCGTTCAACTAA | 9886 |
rs551967511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940787 | AAATTTTTTTCATGC[A/G]TATATGGAATTGCAA | 9886 |
rs551991310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894522 | TATTCTGCGCTCAGT[C/G]TTACTTACAATCAGC | 9886 |
rs552050934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911103 | TGCATTAAGTTTCCT[C/T]ATTCTATCTGACGGG | 9886 |
rs552052379 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894583 | GCTTTGAATTTTACA[-/T]TTTTTTATGGGCTGA | 9886 |
rs552059246 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913767 | AAACCCTGCCTTAGA[A/C]GGATGTGAGTTTGAA | 9886 |
rs552076705 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890010 | CATGTAAGCCTCACA[A/G]TAGCCCTGTGAGGTA | 9886 |
rs552080616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897947 | CTGACCTTGTGATCT[C/T]CCCACCTCGGCTTTG | 9886 |
rs552117587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897317 | TTTGAAGACATGGTC[A/G]GAAAAGAATTGATAA | 9886 |
rs552136582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993912 | GCTCAATAGTGCAAT[C/T]AGATTTTCTTAATAT | 9886 |
rs552190890 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893833 | AAACAGTTGTCCAAT[C/T]ATGGTGTTTGATAAA | 9886 |
rs552220458 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931832 | ACAGAAATTGAACCA[C/T]ATAAAAAGACAGCTG | 9886 |
rs552221802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931200 | AAATCCACGTGCTAC[A/G]CATCTCATTCTTTTA | 9886 |
rs552232830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901902 | CTTGGGCCCATCAAT[G/T]CTTTTCTGGGCTGAG | 9886 |
rs552262839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924257 | TATAAATTTCACCAA[A/G]ACACTATTTGAAGAC | 9886 |
rs552288467 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960861 | ACCACTTCAGGAAGA[C/T]TTTTTTGTCACCATC | 9886 |
rs552309074 | in-del | -/AGTA | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969074 | GGATTTCACTTACTG[-/AGTA]AGTGAGATGACAGAA | 9886 |
rs552382119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881415 | AGCGCTAAGTGCTCT[A/G]AGATGTTAGTAATTG | 9886 |
rs552393308 | in-del | -/TA | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912215 | GTGTATATATATGTG[-/TA]TATATATATACACAC | 9886 |
rs552413040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875324 | TGCAGGATGATAACT[C/G]CTGGCCACACGAGAC | 9886 |
rs552414488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990074 | TGCAAGCTCCGCCTC[C/T]TGAGTTCATGCCATT | 9886 |
rs552431837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994557 | CTTCAGTCTTGAAAT[A/G]TCTGCATGATGTTTC | 9886 |
rs552481758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900037 | GGCCCGAGGTAGGAG[C/T]CTGCCTGTGGTGCCC | 9886 |
rs552491483 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945027 | CTCTCTTCCAGGCTG[A/C]CCGTGAGTTCTGAGG | 9886 |
rs552533023 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979689 | GGGAGAAAGACTGTA[A/C]CAACGAGTGAATTAC | 9886 |
rs552540012 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933026 | TCATATGCTCGTTAG[A/G]ACTAGGCTATGCTTT | 9886 |
rs552563351 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977596 | ACTTGGTTCTTTTTT[C/T]ACTGTTAATATTGTA | 9886 |
rs552564306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919009 | CCTCGGCCTCCCAAA[A/G]TGCTGCGATTACAGG | 9886 |
rs552573544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952963 | TGGGAAAACACACAA[C/T]GCAAGCTTTAGTTCA | 9886 |
rs552590063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996291 | TCCAGTTCTTTTTTT[C/T]ACCTGCCCAAGCTGA | 9886 |
rs552603142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912867 | TTTTTGAGGGAGTCT[A/G]TTGTTAAACTAATAA | 9886 |
rs552603701 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002419 | AAAATAAGATGCAAC[A/G]AAATCAGTTTGAAGA | 9886 |
rs552655077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874352 | TCTCAGAATAATCTG[C/T]AAGGTTGGTAGGATG | 9886 |
rs552685218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939030 | TCATAACCTCATTAA[C/T]GCTGGGAACTTGCCA | 9886 |
rs552744948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959525 | GTGCTAGTGGATGTT[A/G]CTCACATGTCTCTGA | 9886 |
rs552748216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947215 | AGATCCATTTTTGTA[C/T]ACTAAAATCATTGCT | 9886 |
rs552808451 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912208 | ATGTGTGTGTGTATA[C/T]ATATGTGTATATATA | 9886 |
rs552813094 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946611 | TGCCAAAGTCTTATT[A/T]TATCACTGACCTGCT | 9886 |
rs552826081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972469 | ATGTTCTCACTCATA[A/G]GTAGGAGATGAACAA | 9886 |
rs552844719 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895077 | GGAATCTTGTGATGA[C/T]AGTAGCACAATGCCA | 9886 |
rs552852406 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958557 | TCAACCATCAACCAC[A/G]TCTTCAACACAGAAG | 9886 |
rs552886973 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956252 | AAAGGTACAGTAAAA[A/G]TATGAATAAAAGACT | 9886 |
rs552923422 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946425 | ACGGCCCTCATATGT[-/G]GGGGGGGCACAGGGC | 9886 |
rs552963814 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881691 | AACTCTGGGTTTTGA[A/C]AATCTTCAGATTACC | 9886 |
rs552976730 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980603 | GAAGGAACCCAGAGT[G/T]TGGATTAATTGTAAA | 9886 |
rs552981802 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922710 | ACCAGCCTGCTGCTA[A/T]CAGCATGGAGTGAGC | 9886 |
rs552995695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917187 | AGCACACTTTAGCCA[A/C]ACAAAATGGCTTTCT | 9886 |
rs552997796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911771 | GGACTGTTATTTTGA[C/T]CCCAAACAGTTTATT | 9886 |
rs552998715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895527 | CCCCTGATTCAGCCT[C/T]CTGAGTAGCTGGGAT | 9886 |
rs553030282 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917865 | CTTACTCAGACATCA[C/T]CTCCCCTGGAAAGAT | 9886 |
rs553034958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906096 | AGAAAAATCAGTGTC[A/T]AAGAATAAACTAGAT | 9886 |
rs553054562 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897538 | ATCTAGAAGCTTCAG[A/G]TCAGGTAAATTTTAC | 9886 |
rs553057811 | in-del | -/CCCATTTACAA | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890450 | GGCTGGCACACAAGG[-/CCCATTTACAA]CCTAATCAAACCCTG | 9886 |
rs553106073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912336 | CCTCCTGGGTTCAAG[C/T]GATTCGCCTGGCTCA | 9886 |
rs553131850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982355 | ATTTAGGTGATGTGG[A/T]GTTCCTTCTCAAATG | 9886 |
rs553146414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925812 | TGGAAAACCTAGAAG[A/T]AATGGACAAATTCCT | 9886 |
rs553170497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974548 | ACATCCATCGAGATT[G/T]GGGGGTCAGTACAGA | 9886 |
rs553173562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979683 | AGATGAGGGAGAAAG[A/T]CTGTAACAACGAGTG | 9886 |
rs553235755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894836 | CCCTATTAAGACACA[G/T]GGCTCTAAGGGGAAT | 9886 |
rs553243066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886300 | CCAAGGCTTCTGCTC[C/T]CATAGCCACCAAACT | 9886 |
rs553247907 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967641 | ACTACTATTGCAGAG[A/T]GGGAAGAGAAGATGA | 9886 |
rs553252873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893239 | TGCTGATGCATTGAC[A/G]TTTCCGATGAAGTTA | 9886 |
rs553254569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952401 | ACTAATTAGCACTTA[A/G]TAAGTACCCACTATG | 9886 |
rs553256159 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989819 | CAGCAATGCAAGCAG[C/G]TGGGAGAGGCAAGCC | 9886 |
rs553273668 | in-del | -/TGTG | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870137 | CCTTGAAATGCTCTC[-/TGTG]TGTGTATGTGTGTGC | 9886 |
rs553274465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900857 | ACGGCAGAGGTTAAC[C/T]GGTTAATCTCTATAT | 9886 |
rs553281354 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002980 | ACATGTGCACAACCT[A/G]CTGGTTTGTTACATA | 9886 |
rs553284856 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994072 | AATGTGACTCAAAAT[A/G]TTAGAAATTATTGCT | 9886 |
rs553349341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925268 | CTCTTTTCTTTATAA[A/G]TTATTCAGTCTCAGG | 9886 |
rs553379004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939218 | AGAGCTCAAGAAAGT[A/G]TCTGAAGACAGGAGT | 9886 |
rs553382167 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888019 | TCCACCTGCAAAATG[C/G]AGACAATCATATTTA | 9886 |
rs553405665 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914679 | ACGGAATGGCTGTGT[C/T]GCTTTCACTGAAGAT | 9886 |
rs553440800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973873 | CCGATGTAGGTGATA[A/C]AATTTTATCTTTGAC | 9886 |
rs553441281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891465 | CCCACCTCAGCCTCT[C/T]AAGTAGCTGAAACCA | 9886 |
rs553502168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928362 | TCAGTATATCAAAGC[A/G]ATATCTGCATTCCCA | 9886 |
rs553516310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968149 | ACCAGCCAATTCAAA[G/T]GTAGCTCCATCTGCA | 9886 |
rs553542373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998132 | ATTTGTCCTGTGTGT[C/T]TGAGGGCGGCCCTGT | 9886 |
rs553600662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884485 | AGAAGTGCTTGAATT[G/T]AATTTTTTTCTTTTC | 9886 |
rs553630984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981707 | TAAAACATGACAATC[A/G]GGAGACTCCTGATGC | 9886 |
rs553636996 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912174 | TTGTATTAATCAAAT[G/T]CATAATTCATAAATA | 9886 |
rs553639036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898151 | AGGAGAGACTCCCCA[A/T]ATCCAGTATATGGAC | 9886 |
rs553716304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950580 | TGTAATTCTGTGCTA[C/T]TTCCTTAACCCACTA | 9886 |
rs553747601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935550 | CTCTAAGTTCTTTGA[A/G]GTATTTCAGTGTAAA | 9886 |
rs553769349 | in-del | -/TA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940898 | TCTTGATTTATTCTC[-/TA]TTGTTGCATACCTGA | 9886 |
rs553778288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985448 | AAAAGAGAAATGCCA[C/T]GCACAGCAATCTGGT | 9886 |
rs553791732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984907 | CTACATACATCCAAT[C/G]TATATGCTAATAACA | 9886 |
rs553803935 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964698 | ATGCCCCAGAAACCA[C/G]AAACTCCAGCTCTTT | 9886 |
rs553850608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977109 | TTAAACAAATTCTGA[C/T]TTAGAATAAAATGAC | 9886 |
rs553903300 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988877 | ATCCTTAATTGTACC[A/C]TTCCTATGAAAGTCG | 9886 |
rs553956632 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936056 | ATGTGTAGGTGTTAC[A/G]CTATGAATAGTACAT | 9886 |
rs553973935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915977 | CATCCAGAAACATTT[G/T]GCCTCTGAAATCTCA | 9886 |
rs554024279 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959224 | CAAGGGAAAGACATG[G/T]CCACATATTTGCTGC | 9886 |
rs554034036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963849 | ATAGCATCTAATAAT[A/G]GTTCTTAGACTATTA | 9886 |
rs554043361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992408 | TCATTACAAGGGGAG[A/G]AATGAAGGACAAAGT | 9886 |
rs554152128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941956 | TTCTCTTTTTCCCCC[A/G]AGAAAGGGAAGAATC | 9886 |
rs554177636 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879195 | TATGATGCGAAAGTG[C/T]ATGTTCAGAATTTCT | 9886 |
rs554216305 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993998 | TATATGCAAAAAATT[A/G]TGTATGTAAATTTTC | 9886 |
rs554238236 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001031 | ATCCCTCTGGCCACC[C/T]CCGCCTCCGCCAGTG | 9886 |
rs554243770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987265 | CTCTTCTGCCTTCCC[G/T]TAAACGTGGGCCTTC | 9886 |
rs554251152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929279 | TGTACCCCATAAATA[C/T]GTACAACTAACATGC | 9886 |
rs554251348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885751 | CATGCTCCTCTTGTA[C/T]TTGGTTTTGATAGTA | 9886 |
rs554259790 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901955 | ACTGGTGCTTGGGCA[G/T]CAGCCAAAATCCTTC | 9886 |
rs554275041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993996 | ATTATATGCAAAAAA[C/T]TGTGTATGTAAATTT | 9886 |
rs554288008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922319 | CCACACCACAAAATG[C/T]AATTAGCTGCACTTC | 9886 |
rs554293345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892720 | GGGATCCAGGAGTGT[C/T]GAAGAGCAGAACACC | 9886 |
rs554304767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981543 | CCCCCTTTAAAATGG[C/T]TTAGCATCAAGTCAA | 9886 |
rs554331339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991733 | ACCGCACCCGACCTT[C/T]CCTCAGTCTTTCATG | 9886 |
rs554332229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899287 | AGTAAAGAAGGCTTG[C/G]TAAACAGACGAAGGT | 9886 |
rs554366958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971668 | AAACACCAAAAGCAA[G/T]GGCAACAAAAGCCAA | 9886 |
rs554369977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992496 | CTCTGGATTGTAGAT[A/T]TTCTGCTGGATATGC | 9886 |
rs554379729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878769 | GCCTGTAGTTGTCCA[C/T]ATAAATGCATGCTGG | 9886 |
rs554411057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985537 | CTGTACAAAATGCTA[C/T]GCACTAAAGAATTTT | 9886 |
rs554433753 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981814 | CGCTTTTGTTGCCCA[A/G]GCTGGGGTGCAATGG | 9886 |
rs554443656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986528 | TAGGTGAAAGGAAAA[C/T]GAAGTCCTATTCTTA | 9886 |
rs554445991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964599 | CAGCATTTTAAACAC[A/G]TCATTTCTTGTTCTA | 9886 |
rs554448366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910537 | AGGGTGACCAAGTGC[C/T]AAAATAACTTAAAAC | 9886 |
rs554474999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957265 | TCAAATACTATGTGC[C/T]GTACCTAATTGTATT | 9886 |
rs554556068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937344 | AACACGTGACAAAAA[A/G]AAAAAACAGGAGCAG | 9886 |
rs554565595 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979059 | ATTTATGGCTTCCTT[G/T]TCATCAGTAGGTAGG | 9886 |
rs554570988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929882 | TAATAAATATCCCAC[A/G]TTTTTTAAACCTACA | 9886 |
rs554589814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936571 | GGCGGTCTGGTTATG[C/G]CCTATTAAGCATGAA | 9886 |
rs554591118 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876485 | GGTACTAGTCTGAGA[A/T]TGATCACAAACCTTG | 9886 |
rs554593209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978680 | GCTCGCATCCAGAAA[C/T]GTCATTCGAGGGCAC | 9886 |
rs554607767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922821 | TTCCTCCAGCCCACT[C/T]AACCAGACCCTTTCA | 9886 |
rs554624019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879264 | GTTTGAGTTACAGAA[A/C]AATAAAGCATCATAT | 9886 |
rs554629903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971768 | AGGCAACCTACAGAA[C/T]AGGAGAAAAATTTTG | 9886 |
rs554675658 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945218 | TGAAACCCATCACTC[C/T]TAGCCTGTAAAGAGA | 9886 |
rs554692922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937903 | GCACCTACTATGTGC[C/T]TTACATGCATGAGGA | 9886 |
rs554693894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994807 | TATTGTTCCATCTCA[A/T]AAGTTTATGAGCCAA | 9886 |
rs554707766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904055 | GCAGCCACCACCTCC[C/T]ACACTCAGGTGATTC | 9886 |
rs554732945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979762 | TCAGAAAAGGGAACT[A/G]GGAAGTGTGGGAAGA | 9886 |
rs554761621 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965397 | CCTCAGTTTATAGAT[-/G]AAAAAAATGCTTTGG | 9886 |
rs554772777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917109 | CAGAACTATAAGAAA[A/G]TAAACTTTGTTTTAT | 9886 |
rs554772845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910572 | TAACAGAAGGCAAGT[A/G]AAGTGTTACTCAGAG | 9886 |
rs554776488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60942006 | GCCAGTGTTAATGTG[G/T]CATTTCTTTGGGTCA | 9886 |
rs554827851 | snp | A/C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923722 | ATAATTGAATCATGG[A/C/G]GGTGGTTTACTCCAT | 9886 |
rs554877889 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964894 | AGGGATAATATCTAA[C/T]GTAATCCTACCTTAT | 9886 |
rs554878115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000495 | AGGCACATAAAGAAG[C/T]AGTCAATTTCTCTAA | 9886 |
rs554905745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899708 | AGGCATTCTTCTAGA[C/T]ATTGGGGATAGAGTG | 9886 |
rs554921604 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944705 | GGCCGCGGACTCCGA[A/G]GGAGGACATTGGCTT | 9886 |
rs554951153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935597 | CTACACCAGATGATC[C/T]ATATGATCTGTGCAG | 9886 |
rs555022506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902211 | CATGTATCTTCTGTG[C/T]GCCAGATGATTCAGC | 9886 |
rs555030212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987285 | CGTGGGCCTTCCACA[A/G]GGTTCTCCACTTGGC | 9886 |
rs555050086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980660 | CGAATGATGGGAACA[C/T]ACATAAAAAGTGGGG | 9886 |
rs555065048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987859 | CCCTAACCCCTGACA[A/G]AAGTTGTTTCCTGCC | 9886 |
rs555083702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933540 | GCCTGGCCAACATAG[C/T]GAAACTTAGTCTCTA | 9886 |
rs555099858 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999331 | GTCACAGCTTAACCT[A/G]CTAGTGGTAAATCTA | 9886 |
rs555122227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893444 | AATTTAAACATTACT[A/G]AAAATGTAACAAGTA | 9886 |
rs555152830 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965407 | TAGATGAAAAAAATG[C/T]TTTGGCAATTTATAA | 9886 |
rs555160936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957389 | GCTGTAATGTCACTA[A/G]GCAATAAGAATTTTT | 9886 |
rs555171615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913282 | GAATGGAGTAGAGTG[A/G]TTCAAGGAACAGATA | 9886 |
rs555171967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920066 | ACAAATACACCAGGG[A/G]ACCTCTCCTTTGACA | 9886 |
rs555176983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873000 | CCTTCTGTTGTCTGT[C/T]GCTCTTGATGTTTCT | 9886 |
rs555195367 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001082 | CGCGCGCGCACGCGT[A/G]TGTGTGTGTGTGTGT | 9886 |
rs555196753 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967378 | GCTCACCGCAATCTC[A/C]ACCTCCTGGGTTCAA | 9886 |
rs555208680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913857 | CCTCAGTCTCCTCAT[C/T]TGTTAAGTGGGTATC | 9886 |
rs555232363 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951822 | AATGATTTGGGAGGC[C/G]AAGGCGGGCAGATTG | 9886 |
rs555277263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951316 | TTTCCTTAATTGGCA[A/C]CACCACTCCTTTCAT | 9886 |
rs555286712 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994025 | TTTCACTGGGGAGGA[A/G]TTTCAAAATTTTAAT | 9886 |
rs555294896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962994 | AAATCTATTTTCTAA[A/C]ATCTAAATAGTCTTG | 9886 |
rs555355854 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889510 | TCTTAGTTTATATAA[A/G]TAAAATTGATTTTTG | 9886 |
rs555372831 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871378 | GTGCCCGAAACCTGA[A/G]CTATGTCGTATCTCT | 9886 |
rs555378036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907507 | GTGGATATAAAGTAG[A/G]TGGTGGAAAAAAGGC | 9886 |
rs555390266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997345 | AAATGCAGTTGTGTG[C/G]GTGCAATCTCAAACC | 9886 |
rs555427052 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990302 | TCAGACTGTTCTATG[C/T]CCAAACTCCATCCTA | 9886 |
rs555430361 | in-del | -/ACCAA | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995981 | CACACTGTGCTAAGC[-/ACCAA]ACAACTTCATTTTAT | 9886 |
rs555460660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902906 | CAAGCTCCTACAAGA[C/T]ACCAGGCCACGTATC | 9886 |
rs555487920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897405 | AAGTACTGTCTTCTT[A/G]GTTTGACTTTCCTTT | 9886 |
rs555492268 | snp | A/T | | | upstream-variant-2KB, intron-variant, synonymous-codon | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945074 | TTTTCATGCATTCAC[A/T]TAAATGCTTATAGAG | 9886 |
rs555552769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960769 | CCTAATGGCCTGCAC[A/C]CTTTGATGTCAGTGG | 9886 |
rs555578404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955763 | TGAATGCAAGGGAAA[C/G]AGGAACCCATATGTG | 9886 |
rs555615323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949105 | GCTAAGTATTGATGG[C/G]TCATAAAGAAAATGA | 9886 |
rs555634190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953204 | CCTCGTGAGTGTATC[A/G]TTTGTTCTCAACTAT | 9886 |
rs555650840 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894887 | TATGACAGACATGTA[A/G]CTAAATGTCAATTCT | 9886 |
rs555655557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962148 | CCTGAGATCCAATGA[C/T]AGGATCGTTGTAAGT | 9886 |
rs555655764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970626 | AGCATAATTATTTTC[A/G]CATTTATAGTAAGCA | 9886 |
rs555662362 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985690 | AATTGAACTAAAAAA[-/C]GAAATATTTCTATTT | 9886 |
rs555677305 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913991 | CATGATGCTGAAGAC[A/G/T]AATGTCTTCAGATGA | 9886 |
rs555678222 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940873 | CAATTCAGCCTTCTG[C/G]CAAGTATAATCTTGA | 9886 |
rs555687612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961407 | GGGGGCAAATAACAC[C/T]GGTGCATTAAGTATA | 9886 |
rs555695150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903417 | TTGATCACTCAACTC[A/G]GCACCCAATTTCTAG | 9886 |
rs555698700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927596 | TTTGACAAAGGTGCT[A/G]AGAACATACACTGGG | 9886 |
rs555748003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934003 | TATAGGATAGGATTA[G/T]AATTCATTTTAATTT | 9886 |
rs555753771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877075 | ACCCAGCTTGCAACT[C/T]AACTCCTCTGGTGTA | 9886 |
rs555796994 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883738 | GTCCAGCGGCAGCTA[C/T]TATTTATTGAATGCT | 9886 |
rs555812424 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886656 | AACCTTACATTTATA[A/C]TATGCTCTACTCGTA | 9886 |
rs555865272 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908961 | GGGGGAGCACTTCCT[G/T]TTTCTATCAAAGGGA | 9886 |
rs555891486 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938286 | TGCTAGTTGTATTTC[A/T]GGCTACATTGGAAGA | 9886 |
rs555892903 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965372 | TCCTTTAAGTGGACT[A/G]TTATTAAGTCCTCAG | 9886 |
rs555906813 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940235 | TCAGCACATTAAAAA[A/C]GATGATATCCTAAGG | 9886 |
rs555927808 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990682 | TTTCTTTTGCTATTC[C/T]TCCATCCTCTGTGGG | 9886 |
rs555973264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907655 | CCTATCAATACTTTT[A/T]TTTGGATAGATGGAT | 9886 |
rs555980834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928144 | TCACCGCAGTTAAAA[C/T]GGCTTTTATGAAAAA | 9886 |
rs555986339 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881355 | TAAGTTGTGAAACTT[C/T]AAAATTTGAACCATT | 9886 |
rs556001230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976868 | AAAGAGTTTAATATT[C/T]AACACACAAAATGTG | 9886 |
rs556028106 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937031 | AGGATAATATAGTCT[A/G]TTCTAGGCCACTTGG | 9886 |
rs556032350 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902921 | CACCAGGCCACGTAT[C/T]GGGGATAGAAAATAG | 9886 |
rs556095835 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948956 | GTTTAGTGGCAGCTT[A/C]CTTGAACAAATCATT | 9886 |
rs556119411 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870888 | TACACATTCTTGGAG[C/T]TGACTTTGTAATTAC | 9886 |
rs556130597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941768 | GACACAGGATGTTAC[A/C]AATCTATAGTCATGG | 9886 |
rs556194874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991156 | TTCACTGATATGCAT[A/G]CTCTTCCCCCTTGCC | 9886 |
rs556206329 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964159 | TAAAAATATAACGCA[C/T]GCAACGTTATTTTCT | 9886 |
rs556211220 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988504 | TTGTTCCATTCTTTA[C/T]GTCCATGTGTACCCA | 9886 |
rs556240583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983854 | CCTCCTTCTGGCCTG[C/T]CCCTCTACTTCTTCC | 9886 |
rs556241442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898092 | TCCATGGTAGGATCC[C/T]ACCTCTTTATATGTC | 9886 |
rs556270825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950483 | TTAAAAAACCAAAAA[C/T]GAAACAAAGATTAAA | 9886 |
rs556277616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976249 | TTTTTTAAAGGAGAA[A/T]ATTTATGTACTTCAT | 9886 |
rs556314348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977009 | AAAATCTTAGCTTCA[C/T]TGGCTAAATTTAAGA | 9886 |
rs556349286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962052 | ACCTGAATTGATCCG[A/C]CGGCCTCGGCCTCTT | 9886 |
rs556357681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914324 | CTAACCCTCTTCGAC[A/G]AGTTTCTGGTTACAT | 9886 |
rs556358032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876747 | ATTGATGCCTCAACT[C/T]GCTCTTTCTATCTAA | 9886 |
rs556377938 | in-del | -/ATCCATGA | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872078 | CAGTCTCGAGGAATC[-/ATCCATGA]GCTGCCTGCTGACCA | 9886 |
rs556417102 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947653 | GTATTGAATGTATCA[A/G]TAGTTCATTCCTTAT | 9886 |
rs556449784 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959698 | TTTCCAGTTATGTGT[A/G]CTTTGGAAAGACACT | 9886 |
rs556493190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959832 | TCTGTGCCTCAGTTT[A/C]CACCTCTGTATAATG | 9886 |
rs556493625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955147 | CTTCCTGGGTTCAAG[C/T]GATCCTCCTGCTTCA | 9886 |
rs556517191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915788 | TTATTGCTGTCATCT[C/G]CTGGACTTCAAGCCA | 9886 |
rs556536355 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869140 | CCCAGATTATACTAA[A/G]TCCTGTAGGATAGTT | 9886 |
rs556539462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915165 | ACACATAAAGAAACA[C/T]TAAATTATGGTAGTA | 9886 |
rs556556157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872405 | TTATATAACTAATTC[A/G]GTAAACCTCTTGTTT | 9886 |
rs556592266 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903607 | ATCACAGGGTATCTG[C/G]TGAAACGTTTCTTGC | 9886 |
rs556631497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993342 | TCAGCTACAAGGGCA[C/T]ATGCCAAAAACAAAA | 9886 |
rs556641358 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894123 | ATCATTAATGAGCTT[-/C]CCCCCCTACATATCA | 9886 |
rs556645911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977934 | AATTAATCATTTACC[C/T]GTTAACTGATATGCA | 9886 |
rs556647650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988960 | TTGCTATCAGGAAGT[G/T]TACAGTCTAGCTAGG | 9886 |
rs556685644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904825 | GTTCAAATTGCTGCT[G/T]TTCTTTCATGCCTTT | 9886 |
rs556687346 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954840 | TTAAAAAAAGGGAAA[C/T]AGTCTTTTATTATTT | 9886 |
rs556700030 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998367 | CTGGGAATACAGTAA[C/T]GAAAAAAGTCAGAAA | 9886 |
rs556718498 | snp | C/T | 4.95356e-05 | 0.00497648 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875005 | AATGCCCACGCCACT[C/T]GTGGCGGCTTTGGTC | 9886 |
rs556738106 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998792 | TTTAAAGGACTTCTC[C/T]GAGGTCAAATGGCTA | 9886 |
rs556743700 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919694 | CTGCATAGAAGTCTA[C/T]GGATGCAAATACTAC | 9886 |
rs556753095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977783 | CTCTGACTTAATGTT[A/G]CATTAACTACTGGTG | 9886 |
rs556795484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971250 | AAGATAATCCTAAGC[A/G]AAAAGAACAAAGCTG | 9886 |
rs556798113 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923005 | AACTCACATTATATT[A/G]AGTAGCTTTGCTTGT | 9886 |
rs556836780 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884409 | TCATTTCTACTTTTT[A/T]AAAAAAGATGTTAAA | 9886 |
rs556854099 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958988 | ATTACTTTGGTGGTC[G/T]CCAGTGAGCCCTGCC | 9886 |
rs556945565 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881620 | TCAGTCTCTTCATCC[A/G]TTACATGGGAGGAAT | 9886 |
rs556980956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889873 | TGTCGACAGTAAGTG[C/T]CTGATAAATGTTAGC | 9886 |
rs556991239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911861 | CATTCAGCCACTGTC[A/G]GGACAGCTGGCACAC | 9886 |
rs556991943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995738 | CTCACTTGTTTCTGC[A/C]CTTATTGTTTTTTGT | 9886 |
rs557016348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952500 | GGCACCACTATTATC[C/T]CCATTTTATAGATGA | 9886 |
rs557036320 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870679 | ACCAGCGCACTAATG[C/G]TATCTTATGTATTCA | 9886 |
rs557039506 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997533 | ATTTTGGTGCTTAAA[C/G]ATAAGCCATCAATAT | 9886 |
rs557044093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883106 | TGAAGGGACGGGAAG[G/T]GGCGAGAATGTCGAC | 9886 |
rs557063033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913012 | GGCTATGGTAAAGAA[A/G]CTGTTCAGAGTAAAG | 9886 |
rs557118578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975338 | GTCCAGAGACTTGTG[C/T]TCCTGGCCCAGAATC | 9886 |
rs557132872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920138 | GTGCCCTTAACTCAC[C/G]TGCTGAAATTTTCTC | 9886 |
rs557141529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924536 | AGAGAGAGACCCTGA[A/T]ATAGTAAGAGCCAGG | 9886 |
rs557149241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876141 | TCATCTGGGCTTTGC[C/T]GTTTTAAGTAACTGC | 9886 |
rs557155664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969138 | TAAAATTGAAGTTGA[C/G]ATGGAACAAATTTAA | 9886 |
rs557160536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989873 | TACCCTGGCTGTAGG[A/C]GCACCACTGATGGGA | 9886 |
rs557195057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874518 | GATTATGTTATTACA[A/G]TCTCAATATTAGCAA | 9886 |
rs557197641 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982443 | TTGTGCTCATTGCAT[A/C/G]TATTACTTCACATTA | 9886 |
rs557225823 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946818 | GCTCACAGGCTTCCA[A/G]AAGATGCTCCTTCTA | 9886 |
rs557233510 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880965 | GGATTAGTGATATGG[C/T]TTGGCTGTGCCCCAC | 9886 |
rs557238884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887163 | AGGTGATTTAATCAA[C/G]TCTACCTAAAGCTCA | 9886 |
rs557243498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946612 | GCCAAAGTCTTATTT[G/T]ATCACTGACCTGCTT | 9886 |
rs557260651 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970601 | AAACTTTAGAATCAT[G/T]TTGGACAGTAGCATA | 9886 |
rs557284154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939246 | AGTGTCCTGGGACAT[C/G]TGGAAAAAGTGGCAG | 9886 |
rs557297727 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953183 | CAACATGGGTAAGGT[G/T]AGCCTCCTCGTGAGT | 9886 |
rs557305391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925940 | CCATCAAATAAATGG[C/T]CAGGACATAGTTGGG | 9886 |
rs557312021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994654 | CAATGCATTTTATTA[C/T]ACATTAAATTCATTC | 9886 |
rs557327412 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994628 | GAAAGATATCCTCAG[G/T]AAAAAAAATGCAATG | 9886 |
rs557334405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946690 | GTTAAAAAAAGTTCA[G/T]TGTCATGCTTCTCTT | 9886 |
rs557336435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954165 | CTTGAAAGTAGAAAA[C/T]GCCTCAAGCCTGGCA | 9886 |
rs557368235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968331 | TGTTCAATTCAAAAT[C/T]CAAATGTAGTGTGTA | 9886 |
rs557411921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926738 | CATATCTCAACACAA[C/T]AAAAGCAATATACAA | 9886 |
rs557468278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913211 | GGGTATGGAACTGTC[A/G]ACTGTAACGCCATCA | 9886 |
rs557473904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947465 | ATCCTCTCATACTAC[C/T]TCTTCATATTTGCAC | 9886 |
rs557485000 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920719 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCCC | 9886 |
rs557485063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894850 | ATGGCTCTAAGGGGA[A/T]TCATTCTCAGAGCTT | 9886 |
rs557514751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925258 | CCAATTAAATCTCTT[G/T]TCTTTATAAATTATT | 9886 |
rs557532871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946378 | CTAAAAAATAGGGTA[A/G]AAACTCAAAAGAAAT | 9886 |
rs557537211 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953451 | ATACCAAATGAGACA[C/G]TCCTAGGAAACAAAA | 9886 |
rs557558923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938834 | AATCTCTGAGTTCCA[C/T]TTCTTGCCTCTGTAA | 9886 |
rs557590114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919332 | TTTATATTATTGACA[A/G]GAAAAAAGGAAAATG | 9886 |
rs557637618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915314 | TCTGATTTTTATTTA[C/T]GTAGAATGAGAGTAA | 9886 |
rs557684860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940067 | CAATAATAATAGTGC[C/T]GTTATAGAATGTGAC | 9886 |
rs557690260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969905 | CCTTCCTCCATTCTC[A/T]GGTGGACACCTGAGA | 9886 |
rs557708787 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894433 | GCTGGGATAATATGA[A/G]CAAAAATATGCATAA | 9886 |
rs557798173 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871354 | ATGCACAAAAGTGGA[A/G]GAAGATCAGTGCCCG | 9886 |
rs557820347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996553 | TGACCTGATGTCCCC[A/G]AGAGCTTCGGCAGCC | 9886 |
rs557821552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895930 | GATGCAGCTTTGATG[C/T]ATTTCTCCTTACCAA | 9886 |
rs557836979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876786 | GAAGTAGGACAAAGA[A/G]AGGACTTTGATCTCC | 9886 |
rs557892926 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967298 | CTGTTTTTTTTTTTT[C/T]TTTTTTCTTTTTTAG | 9886 |
rs557912478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901715 | TCATCATGAAAAGTC[A/C]ACATACTTAGTTGTA | 9886 |
rs557918344 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962688 | CCTTCGGTAAAGTCT[C/T]AAAACAATTTACCAT | 9886 |
rs557941086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974447 | TTAAGTTCACTATGA[A/G]CAAAATGCCTTTGTG | 9886 |
rs557967906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962102 | CCTAAGCCACTGTGC[C/G]TGGCCCATTTATAAT | 9886 |
rs557970219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908308 | TTAAATCTGGCTTCT[C/G]TCACTGTCACCACAA | 9886 |
rs557993492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912591 | AAAAAATTATCTTCT[G/T]TGTTTTCATCAAGAA | 9886 |
rs557995633 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869215 | GTCTAGTGACATACT[C/G]TATTAGCCAAGAGCA | 9886 |
rs558002038 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918998 | TGATTCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 9886 |
rs558027355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881694 | TCTGGGTTTTGAAAA[C/T]CTTCAGATTACCTTA | 9886 |
rs558049171 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914933 | TAAGGGAAAATAAAA[C/G]GCAGGGCAGAGTTAA | 9886 |
rs558054145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976030 | TCTCTTGTAAGGCTA[A/G]GTAAGGACAAGAAAT | 9886 |
rs558063946 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932841 | TATGGGTGTTTAAAA[A/C]CCCATATTCATGAAG | 9886 |
rs558081010 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967472 | CTTTGTTTGCTTTTC[A/T]GGTTCAAGGAACACA | 9886 |
rs558088847 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882310 | AAGATTAGCTGAGAC[A/T]ATTAGGCTTATAATT | 9886 |
rs558100840 | snp | G/T | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944863 | GGGTCCCCCCAGGGG[G/T]CGTAGGGACGCACCG | 9886 |
rs558116365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982954 | GTGCACATGACATAA[A/G]GCACAGAACTTTTAT | 9886 |
rs558148349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979204 | CTTGTGGAGCTTGTT[A/G]TTTTCATCTGTATCT | 9886 |
rs558168873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879379 | TGAGACAGGGTCTAA[C/G]TCTGTTGCCCAGGCT | 9886 |
rs558174241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927529 | ACACACTGACCAATG[A/G]AAGAGAATAGAGAAC | 9886 |
rs558174248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920347 | TCGAGAAAAAATAAT[G/T]GATGGGAAGCCTGAA | 9886 |
rs558181383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889942 | CCTTTATCAACAGCA[A/T]CTCATACTTGAATTT | 9886 |
rs558203773 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878812 | AGCCAGGCACTGCCT[-/G]GGAGGTGGAGAGCTG | 9886 |
rs558215063 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907999 | AGCACCTAATGTGTT[A/G]ACTGGCACACAGTAG | 9886 |
rs558232152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880007 | CAGCATTTGCATTGT[A/G]TTAGGTACCAGAAAC | 9886 |
rs558287542 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959499 | GATTGCTCTACACAT[C/T]ACAGGCAGCAGTGCT | 9886 |
rs558304409 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898373 | GCATATAGTCTGACA[-/G]GGCTATGCAAACAGA | 9886 |
rs558383075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933905 | ATTTACAGAATAACA[C/G]CACTCCTTAAAACTT | 9886 |
rs558410539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885768 | TGGTTTTGATAGTAC[C/T]ATGCCTGGTGACATT | 9886 |
rs558412759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978783 | CATTGTTATTTTGAA[G/T]AACTACTTATACAAA | 9886 |
rs558421292 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957281 | GTACCTAATTGTATT[A/C]ATATGTTCTATACTT | 9886 |
rs558423222 | snp | C/T | | | nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60985867 | AGGGGGAAAATAAAC[C/T]TCAATTCCATTTTCA | 9886 |
rs558426351 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933730 | GAATGTTCATCATCA[C/T]ATCACTATTTGTGGA | 9886 |
rs558447261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979371 | ACTTACCTAGTTAAA[A/G]TTTATCAATGGTCAA | 9886 |
rs558454802 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982272 | AAGTAGGTAACTTAG[A/C]AGATAGGCCTGACTA | 9886 |
rs558477026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900798 | GCCATTACAGTTCTT[C/T]AGACTGTTAATGCTG | 9886 |
rs558486915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972399 | AGGGACATGGATGAA[A/G]CTGGAAACCATCATT | 9886 |
rs558499145 | in-del | -/T/TT | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904119 | GGCTAATTTTTTGTA[-/T/TT]TTTTTTTAGTAGAGA | 9886 |
rs558551324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893096 | TCTAATGCCATCTCA[A/T]GTCACAATTAAAAAA | 9886 |
rs558573880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930589 | CTTAGCAGAGTGACA[C/T]AGCAGAAAGAAACAC | 9886 |
rs558581375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917140 | GCTACTAAGTTTTGA[C/T]GTTTGTTACAGCAGC | 9886 |
rs558586856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873609 | CAATATGAAATTCTG[G/T]ATCATTACATTTTTC | 9886 |
rs558597167 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971876 | CCATCAAAAACTGGG[A/C]AAAGGATATGAACAG | 9886 |
rs558623661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937106 | ATATCAAAGCAGTAG[A/C]TTTCTTCCGCGTATG | 9886 |
rs558624664 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976831 | ATACATGTTAAATTT[-/GA]GAGAGAATTTCTGGA | 9886 |
rs558639747 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951858 | GGTCAGGAGTTTGAG[A/T]CCAGCCTGGTCAACA | 9886 |
rs558673489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931893 | ACCTCAAACAGAAGA[C/T]GAAAAATTCTTGGCT | 9886 |
rs558689901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943692 | CTGCTAAGGGTGCCT[C/G]TTGTACATTTTCTCA | 9886 |
rs558723601 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001170 | GCACCCTCTGGGGCC[C/T]TGTGCTTTGTCAGAG | 9886 |
rs558724861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936708 | TAATCTCAGGCCCCA[C/T]CCCAGAATTACTGAA | 9886 |
rs558762270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887889 | AGTGTGGTACCATGG[C/T]GGTTTATGGAACAGG | 9886 |
rs558762737 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917988 | TGTACACGCATCCAT[-/AC]ACACATTTTTTTCTT | 9886 |
rs558797552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905997 | TAACTTCAACATGAA[A/G]CTAGACATACAGAAA | 9886 |
rs558801343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894768 | GGAAATATATCCAGC[A/T]CCTAAATGTGTTATA | 9886 |
rs558810587 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902146 | TGTACCAGTTCAGAG[C/T]GCGAAGGACAGTGTG | 9886 |
rs558814527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900255 | AAAGGCAGGAAGAAG[A/C]AGAGGACCAATTAAG | 9886 |
rs558832106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892651 | CCTGTTAGAAGGGCT[C/T]AGGGCACACTCCTCA | 9886 |
rs558863704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894284 | AGCTGCACCAGACCA[A/C]AACAAATAGAGCAGA | 9886 |
rs558884549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917755 | CAGACATTCACCCTG[A/T]AGCACTATCTCTGTG | 9886 |
rs558901376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000891 | CCAAGAAAAATCAAT[C/G]CCGCATCACCTTAGG | 9886 |
rs558913108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874215 | TTCTTAGTTTCCTCA[C/G]AGTGTAAATTCATTG | 9886 |
rs558921558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911713 | CTAAGCCTAATTGAC[A/G]CTCAAGTTTTCTTTT | 9886 |
rs558934014 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915862 | GATGGTGCAGCCCAC[A/G]TCCTAGTCTCACCAT | 9886 |
rs558940528 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001278 | AGCTCTCGCGTCCCC[A/C]TGAGCCTGCGGATGT | 9886 |
rs559020391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899924 | GCTAGGGAGGGCCTC[A/G]CTGAGAAGGTGACAT | 9886 |
rs559042541 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980711 | AAAAGGAAAAACCTA[A/C]ACATTGATGAAAGGT | 9886 |
rs559126478 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972862 | TGCTCTATGGCAACC[C/T]TGCTTGGAAGGTAGC | 9886 |
rs559162649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971888 | GGGAAAAGGATATGA[A/G]CAGACACTTCTCAAA | 9886 |
rs559172028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951641 | GCTCACATCCTGTCA[C/T]GGTATCCATCTTAGA | 9886 |
rs559174476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994856 | ACACTTTAATGCACA[A/G]GAAACCCAAAGCTCT | 9886 |
rs559175847 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959045 | TCAGGACTAAGTGGT[C/T]AGGAATGCAAAGTTG | 9886 |
rs559186611 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930257 | GCAAATTAATCTGTC[A/G]GAGCCTCTATATTCT | 9886 |
rs559193181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873155 | CCCAAACATCAGAGA[C/T]AGTTTTAGCTGGTGC | 9886 |
rs559217800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905616 | ATCCTGTCTTTTTAA[G/T]ATTATTATTATTTAC | 9886 |
rs559262999 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930062 | CTCTATAATATGAAC[A/C]AAAAAATCTCAACCC | 9886 |
rs559264285 | in-del | -/CTAAG | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876348 | CATTTAATAACTAAA[-/CTAAG]TGTTCATAGAAGTCT | 9886 |
rs559272715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905076 | CCAGTACTTGAGTGA[A/T]GAAAATGAAGCACTT | 9886 |
rs559292152 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990871 | CAAGCCCCACACCCA[A/T]AATCCAATGTCTGTC | 9886 |
rs559312343 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954260 | TCCTCTGTAAAATGA[A/G]AGTGCTCTGAGTGGA | 9886 |
rs559330216 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989568 | AATCATAGACACTCA[G/T]CTTTCTTCTCTTACC | 9886 |
rs559378129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918855 | GGGTTCAAGCAATTC[C/T]CCTGACTCAGCCTCC | 9886 |
rs559396742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879440 | CTGGGCTCAAGCAAT[C/T]CTCCCACCTCCACCT | 9886 |
rs559489082 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, synonymous-codon | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944170 | CTCGCCCGGCGCCGT[A/G]GCCGCTCTTCCCAGT | 9886 |
rs559517656 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944935 | CAAATGGCTGAGTGA[A/G]GAGGTGAAATTGACT | 9886 |
rs559526666 | in-del | -/AATATATATGTGTGTGTG | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912186 | AATTCATAATTCATA[-/AATATATATGTGTGTGTG]TATATATATGTGTAT | 9886 |
rs559568789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922484 | AACTGGAAGGATTTC[C/T]GCCAAATTCACTTCC | 9886 |
rs559592676 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969026 | ATAGAAAGTATAAGT[A/G]TGCTAGTTAAATTTA | 9886 |
rs559611455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957541 | AGTGGTGCAGCCACC[A/T]CCAAGCCTTACGGTC | 9886 |
rs559640184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916866 | CAACGCAATCACGAT[A/G]GTCCTTTAAATGCGG | 9886 |
rs559700088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927830 | CTGAGATCTCACAGC[A/G]AAAATGGACAAATGG | 9886 |
rs559719756 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995861 | TAAAAAAAAAAATCA[A/G]GTTCAAGCAGGTTGC | 9886 |
rs559727352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988116 | TTTTTTTGTATTCTT[A/G]TTAGAGACGGGATTT | 9886 |
rs559728272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996113 | TAGCTCGTAAATGGA[A/G]GAGCTCTTACCAGGC | 9886 |
rs559775384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959292 | TTGCTCTTGGAAAAC[A/G]GACCTACAGTATGGC | 9886 |
rs559821682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952205 | GAATTTTAAAACTGT[C/T]TTTTATGGTGTTATC | 9886 |
rs559834747 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931525 | TACTCCATTACTTTT[A/T]ATGGCTGAAAAATAT | 9886 |
rs559852364 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937310 | TGTTTATGCTTTTCC[C/T]ATCAATATATCAGTC | 9886 |
rs559856266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875135 | GGACGACTTAAGAAG[A/G]GAGGAAATGTGGGAC | 9886 |
rs559876307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896989 | AAGCATTTTTTTTCA[G/T]TTATCTTTCGAGGGG | 9886 |
rs559893325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874725 | TGGTGCCTTAGGGGA[A/C]AATGGGACTGGCATG | 9886 |
rs559900137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931077 | AGAAAGCAACAGTAA[C/T]TGTTGCTGGACAATG | 9886 |
rs559944055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914813 | AAGAAGAATTTCTGT[A/G]TCAAAGGTGAGAATA | 9886 |
rs559950876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937638 | TAAAATAATTCAATG[C/T]AAGTAAACTTTGGCA | 9886 |
rs559977836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880464 | TCCCTTAACGTATCA[C/T]AGGGAAGGTTTAGAA | 9886 |
rs559986553 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960109 | GTGGTACTGTAAGAA[A/G]CTTTATAATTTTAGC | 9886 |
rs559995008 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896156 | GAGATATTAAATAAC[-/TT]TTAATCAAAACATTC | 9886 |
rs559996374 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884503 | TTTTTTTCTTTTCCA[A/G]CAGTTTGTAAAAAGA | 9886 |
rs560004631 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955364 | GAACCTTCTTTATGG[G/T]TTTAAAATGCCACAA | 9886 |
rs560011958 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947520 | TCTCCATCTCTAGAG[-/T]TTTTTTTATTGTGAG | 9886 |
rs560019168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886720 | TTTTAAGAGATGTGG[C/G]GGGGGGTGGGTCTGG | 9886 |
rs560029324 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940334 | TTAACAACTGTTACA[A/C]ATTACTCTACGAAAA | 9886 |
rs560035568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923996 | GAAGAACTGAGGAGC[A/G]GAGTGTGATTTAATA | 9886 |
rs560039916 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897728 | AATTTTTTTTTTGAG[A/G]TGGAGTCTTGCTCTG | 9886 |
rs560053482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940576 | GCTTTCTCAAAGATG[C/T]TGTGCAGATTCAAAC | 9886 |
rs560058723 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927244 | CCATGTTCATAGATG[A/G]GAAGATCGATATTGT | 9886 |
rs560090230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933709 | GTCAAAAAAGAAAAA[A/C]AAAAGGAATGTTCAT | 9886 |
rs560140412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883988 | CCCAAGCTCAGGAGA[G/T]ATTTTCATTAGTCAC | 9886 |
rs560188366 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934785 | TAGAGAGAACAAATG[A/C]AGATATCTTGATGAA | 9886 |
rs560210871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890304 | TCTTCACACCCACTC[C/T]TCACATTTTAGTCCA | 9886 |
rs560213853 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894187 | AAATTTCTAAAAATA[A/G]TCACTTGCAATGCAG | 9886 |
rs560238126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970241 | GTCTATTCCAATTTT[G/T]CTTATTATATTAAAA | 9886 |
rs560248845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891769 | AGGGAACTGACATTT[C/T]AAAAGAAACGTATTT | 9886 |
rs560250902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935049 | TACAAGAATGTTCTT[A/G]GCAGCACTATCCAAA | 9886 |
rs560268010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878119 | AGTGGGCACATTTTC[A/G]GGCTATGCTGCTTAT | 9886 |
rs560268971 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923435 | ACCAAATTGAAAGCC[A/G]TGCTGGCAACAGTAC | 9886 |
rs560274235 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921716 | TCCACCTGGGGCTGG[C/T]AGAGAACTTGCATGC | 9886 |
rs560274890 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945907 | CTTCCCGGCCCAGGC[A/G]GGTGGCTCACGCCTG | 9886 |
rs560360955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983958 | AATGAAGACGTTTAC[A/G]ATTTTTATCACTTAC | 9886 |
rs560381426 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890645 | CTTACCTTCTTATAT[A/C]AATATTTGGCCTTTA | 9886 |
rs560384965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978858 | TTGATTCTCAATGAC[A/G]AAACATATCAGACAT | 9886 |
rs560434774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934162 | TGAGAAAACATTCTT[C/T]CTTCATTATGTGAAA | 9886 |
rs560488595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992777 | CATTGAAATAAGAAA[C/T]GCCATCTGATTTTGA | 9886 |
rs560540265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936015 | AACAGTGTTAATAAT[C/G]GAGATTAAACTTTAA | 9886 |
rs560544026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968083 | TCTGAACCCTGTTCT[A/G]CCTTCCTCTTGTTTT | 9886 |
rs560550163 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904100 | CCCGAGTAGCCACAA[C/T]ACCTGGCTAATTTTT | 9886 |
rs560559957 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001009 | TGACAGTGACTTTAT[C/T]TCTCTAATCCCTCTG | 9886 |
rs560577888 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877487 | GAGTCAGGGTTTGAT[C/T]TTAGGCAATCTGGCT | 9886 |
rs560590500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892309 | CTATAGGTCCGAATG[A/G]TTTTCAAAAAGTGGA | 9886 |
rs560607686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909257 | CACACCAGCTTTACG[C/T]TGAGGGGTCATGTTA | 9886 |
rs560620644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885576 | GTATTGTAGCACATG[C/G]TAACCTGAAGGACAA | 9886 |
rs560639912 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983783 | TGGGTACCTTCCCCA[A/G]TGTCTGGCCTTGCCT | 9886 |
rs560676401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980860 | AAAGTGTCAAATTTC[A/T]TAGTAGGAATGCCCA | 9886 |
rs560677894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929498 | AACACCTAGAGATAA[C/T]TGAAAATTAAATACT | 9886 |
rs560708191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890693 | TAGGACAGACACTGG[C/T]CTTAGGAGGAAAAAG | 9886 |
rs560709099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872117 | GTTCCTTTCCAGGGA[C/T]ATAGAAGATAAAAGC | 9886 |
rs560764268 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898317 | TAGGTTCTTTACAGA[A/G]ACATTTTCAAAACCA | 9886 |
rs560781987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999092 | TCTTTTATTTTTCAC[C/T]TAGTGCACTTTCACC | 9886 |
rs560796183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872599 | CTAGTGCTAAACAAC[C/T]GTGGCCTCTGGAAGG | 9886 |
rs560831205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884598 | CTAACTGTCCATCAA[C/T]AGATGGATGAATAAG | 9886 |
rs560841703 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949504 | CAGATCTCTAAAGCT[A/C]CTATTTTCTTCCCAC | 9886 |
rs560867896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891616 | GCCTCCTGAAATGTT[A/G]GGTTTACAGGCATGA | 9886 |
rs560921117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936889 | TTGGTGAGTTCTCAG[C/T]ACCTAGCCCCAGTTC | 9886 |
rs560921160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929687 | TTCATAATAGAAGTA[A/G]CATGAACCTTCATAG | 9886 |
rs560922667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921785 | TGAAAGCAGCAGCGT[A/G]TGGCTAAGCCTGCAG | 9886 |
rs560933765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927992 | TCAACAGAAAAAAAA[C/T]CCAATTTAAAAATGG | 9886 |
rs560944348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964084 | ATGTGTTAAGGCAGG[C/T]AATACATGCAAACAT | 9886 |
rs560948691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956068 | TTCATCGTTGTGCAA[A/C]CATCATACAGTGTGC | 9886 |
rs560977487 | snp | A/G | 0.0006606 | 0.0181621 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872157 | AGGTGAGGAGAGCTG[A/G]ATGAATGGGGGCCTC | 9886 |
rs561010831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877456 | CAGGACAAAGTCACC[A/T]GGTCAGTAAATGGTG | 9886 |
rs561028223 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927978 | GCAGCTCAAACAACT[C/T]AACAGAAAAAAAATC | 9886 |
rs561037620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934339 | GTTCCTGGTTATTCA[C/G]CTCCCTTTACTTATA | 9886 |
rs561046792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884059 | TAAGAGGCCATCAGG[A/T]TAACTCTAATATTTT | 9886 |
rs561052310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965039 | AACTTTAGGGTGATA[G/T]GAAGAGTGAGTTACT | 9886 |
rs561073408 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934767 | CCAAATCTCATCCCT[A/C]TTTAGAGAGAACAAA | 9886 |
rs561205139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977339 | TTCATGGGGTGTTGC[C/T]CTATTTATGAAACCT | 9886 |
rs561228859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972522 | GGGGAACATCACACA[C/G]TGGGGCCTGTCGGGG | 9886 |
rs561231118 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988280 | TTTATTTATTTCAAA[G/T]AACTAAGATTTTATT | 9886 |
rs561239507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970895 | TTGTAAAAATATTCA[C/T]GGAGAGTCAAACTCA | 9886 |
rs561259589 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968405 | TTTAAAACAGGAGTA[C/T]GAGCACCAAAATAAC | 9886 |
rs561278617 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936260 | AATCAACTGCAACAT[A/G]GGTTGGCCTATGGAT | 9886 |
rs561282109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928522 | AATAAACCAGGCACT[A/G]AAAGACAAATATTTC | 9886 |
rs561329635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903851 | TCACATAGTGATTTA[C/T]GTTTTCAACGAGACT | 9886 |
rs561389156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885998 | ACAGTATGATGACCA[C/T]TCATGGAGCCAGTTT | 9886 |
rs561400019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972072 | GTGGAGAAATAGGAA[C/T]GCTTTTACATTGTTG | 9886 |
rs561417958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899300 | TGCTAAACAGACGAA[A/G]GTGAAATTGTGGTAA | 9886 |
rs561418419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879552 | GGCTTGCTATGCTGC[C/T]TAGGCTGGTCTCAAA | 9886 |
rs561432051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978419 | GGTTTGCATTTCTCA[A/G]TCAAGTGGAAGTTAT | 9886 |
rs561443273 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925419 | TTCCAAAACCTATGG[A/G]ACACTGCACAAATGG | 9886 |
rs561462044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943888 | CCCCCACTTGCCACC[C/T]GCTGGGGCCGGGGCG | 9886 |
rs561478367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923204 | TAAAAACCTTGAAGC[A/G]TAGACATGTACAAGC | 9886 |
rs561479091 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891968 | TTTATAAAGGGCATC[C/T]GCCTTTGCTCGGTTC | 9886 |
rs561501064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904382 | AAATGGCAAACATTT[C/T]CATCACCCCTAAAAT | 9886 |
rs561501495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992978 | ACTCCTATCCAAGGA[A/G]ACTAAGGTTAGCAGG | 9886 |
rs561517992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993600 | TTTCAGTATGAATCT[C/G]TCTCATGGCCCTATC | 9886 |
rs561536505 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60985892 | TTTTCATAACTTAGT[C/T]AAGAATGCTTGATGA | 9886 |
rs561536899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912661 | TTACTTTGGAATCTT[C/T]CTGAGACCATCCAAG | 9886 |
rs561538913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933042 | ACTAGGCTATGCTTT[A/G]ATTCAGGCAAACAAG | 9886 |
rs561556999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892401 | AAAACCCTTCAATAT[A/G]TGTGTTTGTATGAAT | 9886 |
rs561559056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982652 | CTCCTGATGGGCAAA[A/C]TTTCCTCCTATTGGG | 9886 |
rs561626307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896107 | ACCTGCAGCTAAGAA[C/T]ATCTCCAGCTTTAGG | 9886 |
rs561648272 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946135 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 9886 |
rs561655094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990021 | GGAGTCTCGTTCTGT[C/T]GCCTAGGCTGGAGTG | 9886 |
rs561655601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899011 | TGGTTGGTTCTACCA[C/T]CATAGTACAAATATC | 9886 |
rs561678537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926057 | CCAACATGGTGCACC[C/T]CGTCCCCCGTCTCTA | 9886 |
rs561682090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938965 | GAGTTTGGTCTACAG[C/T]TGGGTACCAATTCAA | 9886 |
rs561683963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947048 | CCCCAAACTTTACTT[A/G]TAAAATCTCAGACTG | 9886 |
rs561711918 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939383 | GTTCTATTTGTTTAC[A/G]AACTAAAAATAAAAA | 9886 |
rs561724660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997784 | ACATACTAAGATGTT[C/T]TAATGCTGCTACTCA | 9886 |
rs561746652 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985155 | CCTTTTAAATATGCA[A/T]TAGAACATATAAACA | 9886 |
rs561762897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906721 | AAACTGTAGTTGTTA[C/T]CACTGTCAGCAACAT | 9886 |
rs561788699 | snp | A/C | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912897 | AGAACAGATGCTACA[A/C]TTGATCTTAGCCAAA | 9886 |
rs561798421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991268 | CCCCCACCAAAAAAA[C/T]GATAAACAACAAAAA | 9886 |
rs561822555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975534 | AAATGCTACTTATTC[A/G]CTTGCATGGAAATAC | 9886 |
rs561835441 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876284 | TATAAAGGATTAAAG[A/G]AATCATCTTGGGAAG | 9886 |
rs561837380 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909810 | GCTTCCATAACTCTC[G/T]GAGTCCCCTTGAAAG | 9886 |
rs561841692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897818 | TTCAAGCAACTCTCC[G/T]GCCTCAGCCTCCCGA | 9886 |
rs561873792 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991371 | GGACCTGATGACATC[C/T]CCAGACTTAAGCAGT | 9886 |
rs561879133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897068 | AACATAAGGAGTACA[C/T]GCAAAGTTGGGACCA | 9886 |
rs561893633 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931328 | TTGTGCCCACTAGCA[C/G]TCATTCTTTATTCTC | 9886 |
rs561894528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947849 | TGTGGGATGAATACT[A/G]AAGAATGCAATTGCT | 9886 |
rs561898168 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869369 | ACCCTTAATGTTTTG[A/T]TAATTTAAAAAAAGC | 9886 |
rs561912959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906343 | TTGTTGTGGAATAAA[A/G]AATTTAAGAGGAACA | 9886 |
rs561930150 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907789 | ACCAATGTAGGGTCC[C/G]AGTAGGTTGAGGTAG | 9886 |
rs561960430 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895251 | GGTTGTGCTGAGAGC[A/C]ATACTACCTCTGAAG | 9886 |
rs561985876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961226 | AAAAATGTCCTTGTG[A/G]ACATATAGGAAACCT | 9886 |
rs562013368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901804 | ACGCAGAACATAAGA[C/T]ATTAATGTACTGAAC | 9886 |
rs562022642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961792 | CTATTAATGCAGTGG[C/T]GATTTATAACCTTTT | 9886 |
rs562055497 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870608 | AATCTGCATGCAGAA[A/G]CATGGCAAGTTCAAG | 9886 |
rs562058281 | snp | C/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883560 | ATGCACTTCAGTGAG[C/G]TGGACAAAGAAGGGG | 9886 |
rs562074496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955277 | TGAACTCCTGATCTC[A/G]TGATCCGCCTGCTTC | 9886 |
rs562095263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908434 | CACTGAACTGTAATT[C/T]TCACTAAGTACAGTA | 9886 |
rs562110433 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932120 | CATGTATGTATTTGT[A/G]TACCTGGAAATCACA | 9886 |
rs562127773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998217 | ACACTATAAGATCAA[C/T]GATGCTTCATTTAGG | 9886 |
rs562146122 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955445 | CAAAAAAATGCTGTA[A/C]AGACATGGATCAATC | 9886 |
rs562236156 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897726 | ATAATTTTTTTTTTG[A/G]GATGGAGTCTTGCTC | 9886 |
rs562242218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962963 | AAATAATCCCCAGCC[A/G]TGTTGTTAGGACTGA | 9886 |
rs562250256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919843 | AGATCAGTGGGGGAG[A/G]TGAACCAAGATTAGA | 9886 |
rs562266141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954628 | AGTGTCAGTGGTGTC[A/G]CGTATTCTTATTTGA | 9886 |
rs562282232 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989467 | ACGTTGATACTTGTT[A/G]AATGAATAAATGTTT | 9886 |
rs562285740 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920464 | CAGGCCTGAAGAGCC[C/G/T]GAGGGATAGGAAGTG | 9886 |
rs562287026 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927028 | ATAGTAAAGTTTCAG[C/G]ATATGAAATCAGTAT | 9886 |
rs562293671 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909155 | AGCTGGACGGGGCCC[A/G]GTGTGGATCTATGAA | 9886 |
rs562428386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969597 | AGAGACAGATTATGG[A/C]TCAATTAGGATTTTC | 9886 |
rs562435726 | in-del | -/GAGGG | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905503 | AAAAAAATCCATGGT[-/GAGGG]GGACAAAGTATCAAA | 9886 |
rs562442177 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961077 | CTAGCCCTTCAACCA[A/C]CCAAAGGAAAGGGGT | 9886 |
rs562464582 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924772 | GTCTCAAAAATTTTT[A/T]AAAAATTATATCCAG | 9886 |
rs562476558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933160 | CTTTATTTGAAGTTA[C/T]TGGCTAATAACAATG | 9886 |
rs562500730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947161 | AACGCCTGTAATCAC[A/T]GTCATGAGTTTATCT | 9886 |
rs562510570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901846 | TCCTTATTCTCTTTG[C/T]CCATTGCAGTGGCCT | 9886 |
rs562522145 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929983 | CAAATCCCCCAAAGT[A/G]TAAATTGTTGTCAAC | 9886 |
rs562550609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883794 | TCTTACACCCCACAA[C/T]CACAGTATGGGTTAT | 9886 |
rs562558371 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973218 | CTATCAAAAGGTTCT[C/T]ATCTGTTAAACACTC | 9886 |
rs562560293 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926946 | AGTCAAATTATCCTT[G/T]GTTGCAGATGATATC | 9886 |
rs562578935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984052 | AATCTCTCTAACTTT[C/T]TGAATTGTTGTACTC | 9886 |
rs562588166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883449 | GATTAGCATTCGTGA[C/G]GTCAGCTCTGACAGT | 9886 |
rs562617152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985218 | AAATAACAAATAATT[A/T]TATGGGTGGACAAAG | 9886 |
rs562641318 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980159 | TAAATTCATTAAAAT[A/T]AATAGTTCAACTCTC | 9886 |
rs562657521 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965915 | GAGGAACTGATATTT[-/A]AAAAAAAAATCAAAT | 9886 |
rs562689862 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938748 | GGGGGTTTGTTTAGA[A/G]CAAATATATATTCAA | 9886 |
rs562726522 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983881 | TTCCATCTCCTAATT[G/T]CAGTATCTTTTTCAA | 9886 |
rs562734324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991384 | TCCCCAGACTTAAGC[A/C]GTTCACTCCTCTTCT | 9886 |
rs562740917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982778 | AATGCCTTTCTCACA[C/T]ATAGTAAGTTACAGG | 9886 |
rs562764544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889574 | TTAATAGGTTAATTC[C/T]GATAGCTTTTTTTGT | 9886 |
rs562775148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990414 | ACAGATGCAAGACAT[A/G]AACACGTAAAATACT | 9886 |
rs562778654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983064 | CTAGATGGTCTATTC[G/T]CAGTGTTCTTGAATC | 9886 |
rs562793237 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896880 | TAGAGGAGTGGGAGT[C/G]AATCAGAGAGACCAA | 9886 |
rs562834734 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900284 | AGAGGTAAGAATTCC[A/G]AGAGAGAGGATGGTG | 9886 |
rs562836021 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903572 | AAATTTTCACAGAAC[G/T]TGGTGTTCTCTATTT | 9886 |
rs562856790 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902428 | TAAAAAATGTTTCTC[C/T]ATATAATTATTCTTA | 9886 |
rs562867341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890771 | GAAAATTATAGGGTG[C/T]TGACAAAGGTGGAAG | 9886 |
rs562867875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909061 | GAGTCACAGGAAAGA[A/G]CAGCTTATTTTTGTT | 9886 |
rs562872183 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903083 | TACGGAGAGACACCT[C/T]ACCTGGATTCCGAAG | 9886 |
rs562874354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934367 | ATATCAAAGGAACTA[A/T]TACCTCAATAGGCCC | 9886 |
rs562893223 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983521 | TTTAGGATATCATTT[C/T]TTTCTTTCTTTTTTC | 9886 |
rs562895717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998857 | AATGTGAACTCTTCT[C/T]AGAGACTGCAACGCA | 9886 |
rs562959233 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926459 | CCAATATATCTAATA[C/T]ACATAGATGCAAAAT | 9886 |
rs562978703 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871183 | GCTGAATTTTTTTTC[C/T]TTGTATAAAAAGAAA | 9886 |
rs562980513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987712 | ACTTCTAACAGCTCT[C/T]CAACAGACCTCAACA | 9886 |
rs562991070 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970199 | GTCAATGCTATAATT[A/T]AAAAAATTGGTTATT | 9886 |
rs562994733 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948322 | TCAATTTTATCAAGA[A/G]CATTCTTAGGTAAGA | 9886 |
rs563016826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988339 | TTTATATTCAAGGGA[G/T]ACATGTGCAGGTTTG | 9886 |
rs563025552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898284 | TTCAAGCTTCTTTTT[C/T]CCTGCTGGTAACTGA | 9886 |
rs563086017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920984 | ATGAGACAGTGTCTC[A/G]CCTTGTTGCCCAAGC | 9886 |
rs563114661 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998332 | CAACAACTATGTGCT[A/G]TTCATCACTGTGCTA | 9886 |
rs563136375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908537 | TAATTATGATTCCTC[A/T]CCTTCACAAATGATA | 9886 |
rs563172026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995129 | TTCTTGAACTAAATT[A/G]TTTATGAGTATATCA | 9886 |
rs563186760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957554 | CCACCAAGCCTTACG[A/G]TCAATACAAATTCCC | 9886 |
rs563214425 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875192 | AATCCAGAAGCTGCT[C/G]TGATGTGTGGTCTTT | 9886 |
rs563230307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894453 | AATATGCATAAATAT[A/G]TAAATGAAAAGGAAA | 9886 |
rs563252260 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945014 | CACAGAAACTTCTCT[C/T]TCTTCCAGGCTGACC | 9886 |
rs563305603 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943132 | ACAGTCAGCTCCAAA[C/G]GCACAGCTTGTGTGC | 9886 |
rs563320208 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923727 | TGAATCATGGGGGTG[G/T]TTTACTCCATACTGT | 9886 |
rs563359094 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917416 | TGCCATAACAAAATA[C/T]CATAGACTAGGTGGC | 9886 |
rs563401843 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906804 | GAAATTTTATAGGGG[A/G]AAAAAAAAACAATAA | 9886 |
rs563403217 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938116 | AAGACAGCTTAGAAG[C/G]GTGTTATGTTTTGAA | 9886 |
rs563428937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893726 | CAGGTATATGGGGAA[A/C]AGAAAAACTGCTTTA | 9886 |
rs563436210 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950504 | AAAGATTAAAGGGAT[C/G]AGAGGGTAACAGAAA | 9886 |
rs563495067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887433 | TTACACACACCCACA[A/C]ACCAGCCCAGAGAAC | 9886 |
rs563495806 | snp | A/G | 1.65564e-05 | 0.00287714 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910988 | CCGAGAACGCTCCAA[A/G]ACCTGCAGGAGAGAG | 9886 |
rs563519149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918947 | GATGGGGTTTCTCCA[C/T]GTTGATCAGGCTGGT | 9886 |
rs563557557 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001733 | CCCCAGGGCTGTCAC[C/T]CGCTGGCGCGTGGGG | 9886 |
rs563586884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981773 | CTTGGTATTATAAGT[G/T]ACTTTTTTTTTTTAA | 9886 |
rs563618239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882004 | AATAAACTAAGAACA[C/T]TTTTGGAACATGCAT | 9886 |
rs563629989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960284 | TCCATAGAATTTCCA[C/T]AGAATGTAATTAATG | 9886 |
rs563633278 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869555 | ACTTGGTTACAGTAG[C/T]TGATAACAACACTAG | 9886 |
rs563639207 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000416 | GGGAGACCTTCTCAC[A/C]AAGAGCAAGATGATG | 9886 |
rs563668832 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945602 | AGTCCAGTGGATATT[G/T]CTACTCTTCCTCACT | 9886 |
rs563689318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884910 | GAATAAATTCTAGTG[C/T]ACATTTTTTTTGTCC | 9886 |
rs563705424 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946119 | GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCGC | 9886 |
rs563759344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996190 | CCTTTAGTTTGATCA[C/T]GTTCTCCCCACTTAC | 9886 |
rs563766072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952945 | CAAAGAAAACACAAT[C/T]TGTGGGAAAACACAC | 9886 |
rs563814659 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875755 | TAGAAGTAACAAAAA[A/T]GCAGTAGGAAGAGCC | 9886 |
rs563821870 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918746 | ATTTCTTTTCTTTTC[C/T]TTTTCTTTTTTTTTT | 9886 |
rs563835288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946351 | CTATTTCTCATCAAA[C/T]TGCCCTGGCAGCTAA | 9886 |
rs563843461 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872887 | GATTAAAAAAGACTA[C/G]ATCCTCAAAAATCAA | 9886 |
rs563876986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925391 | TGAAATAAATGAAAA[G/T]ACAAACACAACATTC | 9886 |
rs563880054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932152 | ACACATAAATATTGA[G/T]GTACACTCAGTGCCC | 9886 |
rs563921688 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995790 | AAGGGAGATTTTAAA[G/T]CTATATTCAAATCCA | 9886 |
rs564069031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932201 | TTTACTTAGGCAGAC[A/G]TCTACACATTTTCAG | 9886 |
rs564077529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938207 | CCCACCATATCTTTG[C/T]ACGACTGGAATTCTC | 9886 |
rs564085312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959067 | GCAAAGTTGCCTCAA[C/T]GTTCAAAAATCAGTC | 9886 |
rs564151342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911900 | CCTACTGGATACTCA[C/T]GTTGGCCTGCTAGCA | 9886 |
rs564162129 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939149 | TGTAAAACTTGCTAA[C/T]TCGTTCTTTAGTGGA | 9886 |
rs564239869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902527 | TATTATTCATACAAG[C/T]AATTCACTGTTTAAG | 9886 |
rs564247645 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884314 | TTGTTTTTTGCATTT[A/C]TTTGAAAAGTTTGGA | 9886 |
rs564262894 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893214 | TTCATTTCCATATTG[C/T]ACTGCAGAATGCTGA | 9886 |
rs564276899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901903 | TTGGGCCCATCAATG[C/G]TTTTCTGGGCTGAGC | 9886 |
rs564293725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911600 | CACCAAGGCTTTCCA[A/G]AGCAATCAAAGACGT | 9886 |
rs564312767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913488 | CTTGAAAATTCAGTT[G/T]TAAACTTCTATGGTT | 9886 |
rs564349534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907255 | GAAGGGCCAGATTCC[C/T]GATAAAGGCAGAGCC | 9886 |
rs564363843 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870469 | GGTCTTACAAAGTGA[A/G]GTTGGCCACAGGTGA | 9886 |
rs564366793 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928341 | AAAACAAAAAAAAAA[A/G]GAAAATCAGTATATC | 9886 |
rs564386656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974938 | AAATGTGAATAAGAA[A/C]TGACTCATCTCTTGT | 9886 |
rs564427747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942610 | CTGGGGAGCAGAATG[C/T]AGACATTATTTATGC | 9886 |
rs564445361 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906568 | TGCACTCTGTCCTGG[C/T]TGTCTGACCTTGGCC | 9886 |
rs564454120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882692 | AAAGGTGGCCTACAA[C/T]AGCCAAATCCCAAGT | 9886 |
rs564456382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875332 | GATAACTCCTGGCCA[C/T]ACGAGACTATTTAAA | 9886 |
rs564466656 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961706 | GCATTGCTGTATATA[A/T]GAAAGTGCTTTCACA | 9886 |
rs564505379 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953105 | ATGGGAAAGTCATGC[A/G]GAAAAACACACAGCC | 9886 |
rs564557752 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879937 | TGCTTCCGTTCTGAA[A/C]ATGTACAGACTTTTT | 9886 |
rs564559213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999761 | ATGCCCTCCCTGTTA[C/G]GGAATGTTTATGGTT | 9886 |
rs564561856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954478 | CAGTTTTATTATTTA[C/T]TCACTGATTGCTATC | 9886 |
rs564593883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000866 | GCCCGGGGCTTTCAC[A/G]GCTAACAAACCAAGA | 9886 |
rs564609702 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870948 | AACACTCTCCAATTT[G/T]CACTTTGGGAGATTT | 9886 |
rs564685489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964870 | ACTTCAACCTTCTTT[A/T]TAAAAATTAGGGATA | 9886 |
rs564751115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967616 | ATGATGTTTGGAAGG[A/G]AAACGATAGACTACT | 9886 |
rs564787019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993054 | AGAGAACGAGGGCTT[C/T]GGGCATTTTATTAAA | 9886 |
rs564813010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878820 | ACTGCCTGGGAGGTG[A/G]AGAGCTGTAGAGGTG | 9886 |
rs564822998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957032 | TTCACTTAAACATTT[C/T]GCTATATTTATAACA | 9886 |
rs564853910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885455 | ACCTAAGTACCTTGA[A/G]AGGTGTGTTCAGGGG | 9886 |
rs564894817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898102 | GATCCCACCTCTTTA[C/T]ATGTCATCATTGACT | 9886 |
rs564902316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935841 | TATATGGTGAAAGTA[C/G]AATATAATGGTGTGA | 9886 |
rs564916083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930914 | TTCTTGGGACCTGCC[C/G]TTTTTTAAGGGGGTT | 9886 |
rs564933555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872626 | AAGGCACCAGCCCAC[A/G]GCAGAAAGCAGCGAT | 9886 |
rs564950898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923813 | TTTCTGCTTTCACTT[A/G]GATCTCATTTTTTTC | 9886 |
rs564960539 | in-del | -/TGAA | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965648 | TCAAAAATTAATAAC[-/TGAA]TGAATGAATGAATGA | 9886 |
rs564963853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957436 | TTATGGGACCGCTGT[C/T]GTATGTGCTGTTCAC | 9886 |
rs564965464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950091 | TACCAAGATGGTGTT[C/T]CACTGGTCTAGCTCA | 9886 |
rs564980677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970962 | CACCATTTTTATTTC[A/G]GTAAAACTTCAGAGA | 9886 |
rs564991133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924627 | ACATCAGACTTAGTC[A/T]GCACTATAGACCAAA | 9886 |
rs565044262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904546 | TCTTTTTTGCTTGGC[A/G]TCCCTTACTCAAAAG | 9886 |
rs565084447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886627 | ACACCATTTTACTTA[C/T]TAATACTCAATTAAA | 9886 |
rs565085482 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929366 | CATAATAATACATTT[A/C]TGACTTGGGCCAAAT | 9886 |
rs565163247 | in-del | -/TTATTC | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902448 | AATTATTCTTAAAAA[-/TTATTC]TTATAAAGATCTTGA | 9886 |
rs565170465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971362 | ATATAGACCAATGGA[A/G]CAGAACAGAGGCCTC | 9886 |
rs565175887 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931859 | GCTGTGGATATTCAG[G/T]ACAAACACATACAAT | 9886 |
rs565187158 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874359 | ATAATCTGTAAGGTT[G/T]GTAGGATGCAAACTG | 9886 |
rs565206433 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964290 | GGAGAGAAGGTTGGC[G/T]CCAGAGAGGATACAA | 9886 |
rs565242359 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924410 | ACTGTAAAAAGAGAC[-/AAAG]AAGGTCATTATATAA | 9886 |
rs565244354 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971800 | AATCTATCCATCTGA[A/C]AAACTGCTAATATCC | 9886 |
rs565264276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899850 | TGCCAATTAGAAAAT[A/G]AAGCAGGGAAAGGGG | 9886 |
rs565267897 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947870 | TGCAATTGCTAGGTC[A/T]TATGCTAAATAAAAA | 9886 |
rs565307896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987270 | CTGCCTTCCCTTAAA[C/T]GTGGGCCTTCCACAA | 9886 |
rs565308947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899115 | ATCTCATTTTCTATA[C/T]TTGGCAAATCATACT | 9886 |
rs565328321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972556 | GGGGGGCTAGAAGAG[A/G]GATAGCATTAGGAGA | 9886 |
rs565331816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917543 | GCTTGTAGGCAGCTG[C/T]CTTCTTGTGGTGTCC | 9886 |
rs565359264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874005 | ACCAGAGCAATCTCC[C/T]CTGGCCACAGTAGGA | 9886 |
rs565369873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994164 | AATATTTGTTGAGTA[C/T]CTGTGAAATGCCTGG | 9886 |
rs565374220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990469 | GAACCAGTTACAACT[A/G]TATTTCCTGTACATA | 9886 |
rs565400996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958453 | TGAAGAGTAGGAATA[A/C]ATGGATCTATAGGGC | 9886 |
rs565426737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893601 | GACTCTTTACTAAGT[A/G]AGGCAAGAAGGTAAT | 9886 |
rs565445928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943931 | CAGCGGCTGCTCGGA[A/G]AAGTTTCATAGCATA | 9886 |
rs565472500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993739 | CCTAAATCCTTTCCA[G/T]CATATAAATAAAATA | 9886 |
rs565531976 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952688 | GATTACAATGCATGA[A/C]ATCATCCTATATACT | 9886 |
rs565533766 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000247 | CAGCCTTCCTCCTTG[C/T]TCCCAAATGTGTCTA | 9886 |
rs565535313 | snp | A/C | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002141 | AACCTTCTGCACGTT[A/C]GCCTTTGGAGGCCCC | 9886 |
rs565561441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886047 | GCTGTTTACCCACTT[C/T]ATATAAATACACAGG | 9886 |
rs565588995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980051 | GTGAAACAGGGAGCC[A/G]ATGGAGGTTCTGAGT | 9886 |
rs565589691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987005 | TCATTAATGAGTAAG[A/G]GCAGAACTGCAAAAA | 9886 |
rs565638854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943477 | CTCACAACAGACTCC[A/G]TAGACACGGGGTTGC | 9886 |
rs565676668 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992424 | AATGAAGGACAAAGT[A/C]CACAGACATGCTGGA | 9886 |
rs565695890 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990143 | GCCCGCCACCACGCC[C/T]GGATAATTTTTTGTA | 9886 |
rs565704437 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916640 | GGATGATGGGTCATG[A/C]CAACTTTTCTCTTTA | 9886 |
rs565717117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917642 | ATGGGGCTCCACCCT[C/T]ATGGCTTTATCCAAA | 9886 |
rs565724006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978566 | CAGTGTAAACCCGTG[C/T]TGGGACAGTAGCATG | 9886 |
rs565740605 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant, synonymous-codon | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944173 | GCCCGGCGCCGTGGC[C/T]GCTCTTCCCAGTCCC | 9886 |
rs565755932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911640 | AGGGAGTTTTGCCTT[C/T]GTCCAGCCACTTCCT | 9886 |
rs565765816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936559 | CAAATAAAATAAGGC[A/G]GTCTGGTTATGGCCT | 9886 |
rs565790039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910276 | ATGTTCCTACCCATA[C/T]TAATGTCCTTCTAGA | 9886 |
rs565815746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937016 | TGAAATTGCACCACC[A/G]GGATAATATAGTCTA | 9886 |
rs565858930 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945178 | AGGGAGCTTTCAGTC[A/G]GCCTGCTAAAATTAG | 9886 |
rs565880594 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987970 | ACCGAGTCTCGCTCT[A/G]TCCCCCAGGATGGAG | 9886 |
rs565885779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909874 | TGAAATAATTCCTGG[A/G]AATAGGGCAAACTCT | 9886 |
rs565914262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956172 | AACCTGTACAGCATG[G/T]TACTGGATTGAATCC | 9886 |
rs565921793 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878195 | TTGAGGCTGTGCATA[A/G]GAATCCTTCAGTATT | 9886 |
rs565941934 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001922 | GCCAAGTCTGGGGAA[A/C]GTTTCTGGCGATGTC | 9886 |
rs565948187 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961396 | CTCTCCAAAAGGGGG[A/G]CAAATAACACCGGTG | 9886 |
rs565952803 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908061 | TGGCAAAAGAATGGG[G/T]AGAATAGTTCCATTT | 9886 |
rs566004666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942755 | CCAGAGTATGTTTAA[A/C]AAGGTCTAAGCCTTG | 9886 |
rs566010925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903976 | TTTTCTTTTCTTTTT[G/T]TTTTGAGACAGGGTC | 9886 |
rs566021972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966653 | GCACACATTTATTGA[G/T]AAACTTCTTTTTTTT | 9886 |
rs566026577 | in-del | -/A | 0.292114 | 0.246427 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882205 | GTTTCTTTTTTCTTA[-/A]AAAAAAAAAAAGAGT | 9886 |
rs566046016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905365 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGA | 9886 |
rs566065060 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001037 | CTGGCCACCCCCGCC[C/T]CCGCCAGTGTGTGTG | 9886 |
rs566068627 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936744 | ATCTGCACTTTAACA[A/C]GATGCCCATTTTTGT | 9886 |
rs566098008 | snp | A/C | 3.29609e-05 | 0.00405948 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886139 | ACTTTCCACAAATGA[A/C]CCCCCGAACATGGCT | 9886 |
rs566111042 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920622 | TAGGTTCTGATTTGC[G/T]TTTTTTTTTTTTTTA | 9886 |
rs566111454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951143 | CTAACCCTGATCTTC[C/T]GACTATGTGGATGCA | 9886 |
rs566112415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930306 | AATTATCTCCTTCCA[C/T]GGATTGTTGTGAAGA | 9886 |
rs566124133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874065 | CCTCCTCTCCCTGAA[A/G]CCACCTCCTTTCCTT | 9886 |
rs566200589 | snp | C/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945434 | GAGTCCATCCTATTA[C/T]AAGGGATGCTTCTTT | 9886 |
rs566207336 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959251 | CTGCTTAGACTGAAA[A/G]GTTCTTTATGAAACA | 9886 |
rs566225836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879215 | TCAGAATTTCTCTGC[A/G]GTGCTGGAAATGTTT | 9886 |
rs566268622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971715 | TAACTAAACTAAAGA[C/G]CTTCTGCACAGCAAA | 9886 |
rs566299982 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995847 | CACTTCCCCCAAGAT[-/A]AAAAAAAAAATCAGG | 9886 |
rs566311204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985579 | AAGTGGATAGAAGAG[C/T]TATGTTATTTTAGTA | 9886 |
rs566335641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926467 | TCTAATACACATAGA[C/T]GCAAAATTCCTCAAT | 9886 |
rs566344139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965303 | GCATTTATTTTGCTC[A/G]TCTCTGTATCACTAG | 9886 |
rs566361987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907483 | AGAGCTTCAAAAGTT[C/T]ATCCAAAAGTGGATA | 9886 |
rs566362796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873422 | CACATCACTAGGTTA[A/G]GGTCTAATGAATGAG | 9886 |
rs566373146 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886032 | GATTAAAGTCATCTG[G/T]CTGTTTACCCACTTT | 9886 |
rs566374409 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964210 | GTTAGGTACTTAGGA[A/G]TAAACATGTTACTGC | 9886 |
rs566378907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965843 | TCAGGACATCTGATA[A/G]GACATTGTCTTGCCT | 9886 |
rs566393062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954203 | GCTCCTGTGGGAGAA[C/T]TTCCTTGGGCAAGTC | 9886 |
rs566436511 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872409 | ATAACTAATTCGGTA[A/T]ACCTCTTGTTTTGAC | 9886 |
rs566453887 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880937 | ATTTCATTTCTTTGA[C/T]GAAATAATGTTTGGA | 9886 |
rs566472277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920048 | ATGGGTCTACTTTCT[C/T]CTACAAATACACCAG | 9886 |
rs566477622 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932828 | CAAGGCTGTAGACTA[C/T]GGGTGTTTAAAAACC | 9886 |
rs566479444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914201 | AGTTTTGGGTGTGGA[G/T]GGGGCAGGGAGGAGG | 9886 |
rs566500952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961904 | ACCTCCGCTCCTGGG[G/T]TCAAATGATTCTCCT | 9886 |
rs566509814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882452 | TTATGCTTACTGCTA[C/T]ATTAAAAGTAATGAG | 9886 |
rs566517459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976723 | AATGGGTTTTATATT[A/T]CACTATATACAAAAT | 9886 |
rs566553152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977541 | AGAGGCAAATGATAA[G/T]ATTTGTTTACTTTTT | 9886 |
rs566553554 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970567 | ACTAATAAATTTTTG[A/G]TAAAAATAGTTCACT | 9886 |
rs566559455 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913067 | TGTTTGTTTAATTCA[A/T]CTGATTGAGAAAAAT | 9886 |
rs566591702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971067 | TGGGACACTCTTACC[A/G]TCATCATTATCATTA | 9886 |
rs566608154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878373 | TGCCAAGCACCTTAT[A/G]ATACTCTACTGTGGG | 9886 |
rs566608219 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871855 | GCTGGGCACAGAGAA[C/G]CTGAACCCAGGACCA | 9886 |
rs566620801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889738 | GTAAGTTACTTAACC[C/T]CATTAAACATTAGTT | 9886 |
rs566621079 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929899 | TTTTTAAACCTACAA[A/G]AAGACAGCTTTCTTT | 9886 |
rs566623818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933318 | GATACCAGTCTGGAG[A/T]GCGACTAGAAATTTT | 9886 |
rs566648059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982802 | TTACAGGGCTAGAAT[C/G]CATGTAGACTCTCAC | 9886 |
rs566719225 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928201 | TACAGAAAGGGGAAC[A/C/G]CTTGCAAGCTGTTGC | 9886 |
rs566736263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968962 | TCTAATGCTGATGCC[C/T]GTGTTCTTGTTATTG | 9886 |
rs566755398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928736 | GGCAACTATAGTAAA[C/T]TAACAATAATTTATT | 9886 |
rs566756538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875996 | CATGCTTACTTTCTG[C/T]TCCAGCTCTGCATGC | 9886 |
rs566773186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969717 | GATCATCATCTATGA[C/G]CTTTGAAGTCACCTT | 9886 |
rs566824660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928133 | AAGATATAATCTCAC[C/T]GCAGTTAAAATGGCT | 9886 |
rs566906785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908157 | CAACTGCCTACCACT[A/G]ACAACTCCTCATCCC | 9886 |
rs566914368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956824 | GAGGCAGCTGACTCA[A/G]TATTAGAAAGCATTC | 9886 |
rs566920410 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955974 | ATCACAGTGGGCCTC[A/G]TTTGTTAATAGTCTG | 9886 |
rs566928155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990897 | CTGTCTGCTGTCTCC[C/T]GTGATGTCTCAAGAC | 9886 |
rs566943877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908797 | GGGGTCTGTGTCAGG[A/G]CGCCTGGAGGCTGTG | 9886 |
rs567011718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921998 | CAGTAATTGCAGGCA[A/G]GAGGGGCATAGGATT | 9886 |
rs567040515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897362 | TTATTGTTAAATGAA[C/T]TTTCTTCTAAATTCT | 9886 |
rs567049182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933915 | TAACACCACTCCTTA[A/G]AACTTATGTGCCTAA | 9886 |
rs567050572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998311 | TATTCAAACATACTT[A/C]CAGACCAACAACTAT | 9886 |
rs567064070 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954049 | ATAACCACTACCTTT[C/T]TTAAAAGTGTATGTG | 9886 |
rs567072494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991414 | TGCACTCCAGACAGT[A/G]TGGCCTTCCCTCAGT | 9886 |
rs567108303 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927656 | TGGGAAAACTGGCTA[C/T]CCATAAGCAGAAGAA | 9886 |
rs567130388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902908 | AGCTCCTACAAGACA[C/T]CAGGCCACGTATCGG | 9886 |
rs567150139 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957582 | CCCCTCTTCTCCCAT[C/T]CTCAAAACCAACCAA | 9886 |
rs567158188 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946566 | GTTTTCTGATGTCTT[G/T]ACAGTTGCATTTGCA | 9886 |
rs567182200 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934470 | GGAACAAGACCATGG[A/G]AAAACATTCTCTAAT | 9886 |
rs567216348 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977497 | GAGACCAAAAAAGAT[-/G]TCTCATGATCACAAG | 9886 |
rs567269079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914209 | GTGTGGAGGGGGCAG[A/G]GAGGAGGTCACAGTT | 9886 |
rs567278517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998418 | GCCTACATTCTGATG[C/G]GGAAGTAAGGAGTGA | 9886 |
rs567295374 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969686 | TAGCATCACTTCAGT[C/T]GTCAGAAGAGTTTAG | 9886 |
rs567309036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876088 | CACAAACCTCCTCAA[C/G]TAGATTGAACTATTT | 9886 |
rs567310995 | in-del | -/T | 0.00199481 | 0.0315187 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869430 | TCCTTAAAACAAAAC[-/T]GGAGGCATTTTATAG | 9886 |
rs567319229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920069 | AATACACCAGGGAAC[A/C]TCTCCTTTGACAATT | 9886 |
rs567365953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963558 | GGCTCTCCCTTTGTC[C/T]ATCTAGGAAGCTTCC | 9886 |
rs567382652 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975421 | TCTCTCTGTTCTGTA[C/T]TTGCACTATCAAATA | 9886 |
rs567397303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903388 | TAGTAACCAACCCCA[C/G]TGAGAGGACCCACTT | 9886 |
rs567420898 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916246 | CCACAAATCCGCCAT[A/G]TGAGGAAAGTGGCCT | 9886 |
rs567426164 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964010 | CCCCACTGTCTCACA[A/G]CATTCTCTACCCCCA | 9886 |
rs567446636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975745 | TAAGCATCTCTCTTC[A/G]AAATGTTTCATTTTG | 9886 |
rs567457917 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943855 | GGGGCGCTGCTGGCC[G/T]CGTGGCACGGCCCAG | 9886 |
rs567461341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969000 | TTTTTAAAAATCAGG[C/T]ATTTGAATAAATAGA | 9886 |
rs567477804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934584 | GTTTAAAGAATATTA[C/G]AATCTGATATAACGG | 9886 |
rs567498770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969788 | ATTTATTACATCATA[A/G]TATGACTTAGCTTTT | 9886 |
rs567504123 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996692 | CACTCAGCACCCTTA[C/T]TTCTAGAAACTAATG | 9886 |
rs567539198 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993933 | TTCTTAATATTTGTA[A/C/T]ATACACTTTTAGAGC | 9886 |
rs567603467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878439 | CGGAGCTGCAAACCA[C/T]ACTGTTGCTGACATG | 9886 |
rs567614952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935240 | ACAAAAGAATACATA[A/G]GATATGATTTCATTT | 9886 |
rs567624541 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922097 | TGTTAATAATATTTA[A/T]ATATAAGGGTCTCAT | 9886 |
rs567631908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872759 | GTGACTGTCCTATAC[C/T]TCTCCTTTGGTTACA | 9886 |
rs567671236 | in-del | -/GAG | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894597 | CATTTTTTATGGGCT[-/GAG]TTTTCTATTATTCAT | 9886 |
rs567763657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872393 | GAAATGAAGGGCTTA[C/T]ATAACTAATTCGGTA | 9886 |
rs567782988 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959667 | AAAACCTGAGTGCTA[A/G]TTTTGTCTCTGCCAC | 9886 |
rs567799361 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60868940 | CTGTCACTCAGAAAA[G/T]TCCCTCAATGACATC | 9886 |
rs567808769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916679 | CTCAATTTCTTGCAT[C/T]GCATATGTGGTATGC | 9886 |
rs567816607 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885872 | AAGCACCCAGGTGCC[C/T]CCACACCAGTGACCA | 9886 |
rs567819523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960421 | CCAGTTGTAAATAAA[C/T]TACTCACACAAACAA | 9886 |
rs567825446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891238 | TACCATTTACTATTG[C/T]TTGGAGAGCATAAAA | 9886 |
rs567857906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992200 | AATGGATATAAGAAA[C/T]GAAAGTAGGAAGATT | 9886 |
rs567874221 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945722 | GAGGAAAGTTATCAC[C/T]GGCAACCTCATTTGT | 9886 |
rs567921518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881603 | CTCACCCTCTCTCAC[A/C]CTCAGTCTCTTCATC | 9886 |
rs567953685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973498 | TGAAGGAATTCTGAA[A/G]AAAGTAATTTAGGGA | 9886 |
rs567985268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928822 | ATAAATGCTTGAGGT[A/T]ATGGAAACCCCAATG | 9886 |
rs567988300 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936032 | AGATTAAACTTTAAA[A/G]TGTGCTATATGTGTA | 9886 |
rs567989637 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884320 | TTTGCATTTCTTTGA[A/C]AAGTTTGGAAAGATG | 9886 |
rs568068669 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918689 | CCGCCATTGGAATAT[A/G]CTGCATCTTATCACT | 9886 |
rs568153773 | in-del | -/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870196 | CAATGACTGACTGCC[-/T]CACGAAAGCTCCCCT | 9886 |
rs568208213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919148 | TCTCCATTTAGCTGT[A/T]CACAGACAGTCTGAA | 9886 |
rs568232876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894034 | TTTCATTAGATGTTA[A/T]TTTATTGCCATTGCC | 9886 |
rs568262394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980648 | ACTTAGAACATACGA[A/G]TGATGGGAACACACA | 9886 |
rs568299992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931719 | TATGTATATATAAAG[C/G]ATAGAGAGCCTGCTA | 9886 |
rs568311446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990045 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 9886 |
rs568343372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931297 | CAGAATATTTCCATT[A/T]TCCCCCAAAGAAACC | 9886 |
rs568358296 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887684 | CCCCTTGTAGGAAGA[C/T]GGAGGGCCACCAAAA | 9886 |
rs568364655 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869915 | TAATAAATGCCCATC[C/T]GTAATCTAGATAGAT | 9886 |
rs568374876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989840 | GAGGCAAGCCAGCAC[C/T]GCTTCGTGACATTTA | 9886 |
rs568387862 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870833 | ACATGGCACATATAA[A/C]CATATAATTACCAGC | 9886 |
rs568387979 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962250 | TGTAATTCTTTGTTG[G/T]AACTAAAATTAAAAT | 9886 |
rs568395178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894644 | CAGGTATCTGATGAA[A/G]CTCTGCTATAAGCTT | 9886 |
rs568396500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982895 | CCTCTTTCCTCTTCC[A/G]CTCCCTTCTTATGGT | 9886 |
rs568413176 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904978 | AAGTGTGGTTTGGAT[C/T]ACTTTTCCATAAAAA | 9886 |
rs568421635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940029 | TCATGTTGATGAGGT[C/G]TTGGCCTGTAATGGG | 9886 |
rs568432788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975305 | TTTTTCTCTCACCAG[A/G]GACACATTTGCTACA | 9886 |
rs568453129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883050 | AGCCACTTCCCCAAC[A/G]TCAAGCTGAGAGTAT | 9886 |
rs568497838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926686 | AATTCAACATCCTTC[A/C]TGATAAAAATTCCCA | 9886 |
rs568514717 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928797 | GGAATGTTTCTAACA[C/T]AAAAAAATGATAAAT | 9886 |
rs568559465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960659 | TCTGATGCTTTCTTA[C/T]TTATGGGAGATCATA | 9886 |
rs568588611 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981319 | AATAATAACTGTTTT[C/T]ATTTACTCACTTCTC | 9886 |
rs568591474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953127 | CACACAGCCCATTTC[A/T]ACAGATGGAGTTATT | 9886 |
rs568598789 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881367 | CTTTAAAATTTGAAC[C/T]ATTTTAATAGTGAAA | 9886 |
rs568647011 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953744 | GCTTGATGTTTCTTC[C/T]CGATAAAACAGTTGA | 9886 |
rs568667731 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879211 | ATGTTCAGAATTTCT[C/G]TGCGGTGCTGGAAAT | 9886 |
rs568677404 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931825 | ATCAGACACAGAAAT[A/T]GAACCATATAAAAAG | 9886 |
rs568714709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925153 | TGCTCTCCTCTTACC[C/T]TCCACCATGATTATA | 9886 |
rs568790867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939240 | GACAGGAGTGTCCTG[C/G]GACATCTGGAAAAAG | 9886 |
rs568801596 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903021 | CAATTTTCCCGCAAT[A/G]CAGTTATTGCTACGA | 9886 |
rs568805328 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935598 | TACACCAGATGATCT[A/C]TATGATCTGTGCAGA | 9886 |
rs568881184 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968671 | ACATATAAGTAAGCC[C/T]CAAATAAACCATTTT | 9886 |
rs568897597 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974995 | ATGTGTGGCTGAGAG[C/T]TGTATGATCTTAAAA | 9886 |
rs568909688 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870673 | CCGAACACCAGCGCA[C/T]TAATGGTATCTTATG | 9886 |
rs568935982 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970778 | AAATAGGGCTTTTAC[A/G]GTGCAAGATTAATGC | 9886 |
rs568970653 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902658 | CTTTTTCTCCTGGGG[G/T]CAGCTGATCTTTCCG | 9886 |
rs569002667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876748 | TTGATGCCTCAACTC[A/G]CTCTTTCTATCTAAC | 9886 |
rs569026303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974344 | AGATATAAATAGACA[C/T]GAAAGACAACTATCA | 9886 |
rs569037052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883640 | TACCAACTGGATGAG[G/T]TTTTACAAATTGGTG | 9886 |
rs569048698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878268 | AGTGGAGCTGCCTGA[A/C]ACAGCCTGATGTGGA | 9886 |
rs569065018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967923 | AATTTACTTAAGATG[A/T]CTAGGAAGGGAGAAG | 9886 |
rs569070503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973569 | GCTTGCTGAGTTTCA[A/T]ATTCAAAAGAAACAA | 9886 |
rs569166739 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882201 | TATAGTTTCTTTTTT[C/T]TTAAAAAAAAAAAAA | 9886 |
rs569167842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982950 | GGCGGTGCACATGAC[A/T]TAAGGCACAGAACTT | 9886 |
rs569187121 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948656 | AGAAATTTTGGGGAC[C/T]AGTACTAACAGGGGT | 9886 |
rs569197062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890346 | GCTGCAAGAAAAGTC[C/T]TTACATAACACAACT | 9886 |
rs569201785 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930559 | TGGGCCTCATGCATT[C/T]ACATGAAGCACTGTC | 9886 |
rs569205505 | snp | A/G | 5.02121e-05 | 0.00501034 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888552 | CCCCTTACTCCATCC[A/G]GTCAAAGTCTGTGTC | 9886 |
rs569242160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933784 | AAACACAGGAGATGG[A/C]TTAAAAAAAAACTAA | 9886 |
rs569306127 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947320 | ATCTTTAAACACTTT[C/G/T]CATGTTTCTGTTGCA | 9886 |
rs569309616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987158 | AATCACAGCATGAGG[A/C]CTCTTCCTTGAAATC | 9886 |
rs569414876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928077 | ATGAAAAAATGCTCA[A/G]CATCATTCGTCATCA | 9886 |
rs569449905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902079 | GGACAAGGCTGGGTC[A/G]GGCATAGGAATCCCA | 9886 |
rs569488417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896528 | TTGTAAACTCCAGAA[C/T]CTGAATACTGAAAAG | 9886 |
rs569491685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990701 | ATCCTCTGTGGGCTC[A/G]TCTTTCACTACTGGG | 9886 |
rs569582761 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002228 | TAATATTAGAAACCC[A/G]CACATTTATACGTTT | 9886 |
rs569601303 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993673 | TTACCTATTTGAAAT[-/A]CATTTTATATTGCTC | 9886 |
rs569601877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933431 | GATTTCATTTAAAGA[A/G]TGTTCATTGGCTGGG | 9886 |
rs569610214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902763 | GTTATTCTTATTACA[A/G]AAGGGCATATATAAA | 9886 |
rs569630407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937084 | CAGGTACAAGTATTT[A/C]AAAAAAATATCAAAG | 9886 |
rs569647226 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996557 | CTGATGTCCCCGAGA[C/G]CTTCGGCAGCCTGGA | 9886 |
rs569657238 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972757 | TCATCAGCTTAGCAC[A/C]CAATACCAGTAGTGG | 9886 |
rs569700000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912171 | TATTTGTATTAATCA[A/C]ATTCATAATTCATAA | 9886 |
rs569715222 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989845 | AAGCCAGCACTGCTT[C/T]GTGACATTTATTTAC | 9886 |
rs569720663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879877 | TCCACATCTGTGGAT[A/T]CAACCAACTGTAGAT | 9886 |
rs569732760 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976466 | TCTAACTCCGAGTTA[A/G]GAAACTGTATACTGA | 9886 |
rs569765867 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930519 | TGAAACAACAGTAAA[G/T]AAGTATGTGCAACCC | 9886 |
rs569854954 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964156 | TTGTAAAAATATAAC[A/G]CATGCAACGTTATTT | 9886 |
rs569872423 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944294 | GCACCCGGCACCTCG[C/T]TCCGCCGCCGTGGCG | 9886 |
rs569934998 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002865 | TCTTTCTAATAAGAT[A/G]TAATTTAAAGATTGC | 9886 |
rs569970040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995494 | TGATAACCTCATTTT[A/G]TCTTACTGTTTAAAA | 9886 |
rs569975466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899217 | ATAATTTATTAAAAG[A/G]AACAGCTTAAACAGT | 9886 |
rs569987365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936593 | AAGCATGAATTTCAG[C/T]GTAAGATATAGTAAC | 9886 |
rs570011098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900191 | ATGGACTAAATTGGT[A/G]GCAAGGTAAGAGTGG | 9886 |
rs570015285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994817 | TCTCATAAGTTTATG[A/G]GCCAAGTAAATTCTA | 9886 |
rs570044648 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945777 | TTTGAAAATGGAGTT[A/G]CCAAGGCCCTAGTCT | 9886 |
rs570061417 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911671 | TGGAGGTGCACAAGC[A/C]CAGGAAAGAATGTTT | 9886 |
rs570064823 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970494 | ATTGAATATTAATTC[-/T]GTATTTCATAGATCT | 9886 |
rs570081279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938433 | AGTTACGTTGTTTCT[C/T]TGGGTGCCAGTGTTT | 9886 |
rs570091143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900788 | TATAATGTGAGCCAT[C/T]ACAGTTCTTCAGACT | 9886 |
rs570103360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980496 | TTATGACATTGAGAT[A/G]CTCTTCTCAGGTACC | 9886 |
rs570120343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988606 | ATGATGGCCTCCAGC[C/T]GCATTCACATTGTCG | 9886 |
rs570123163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924210 | CTAATGGACACAAAC[A/C]CTCTCCATAAAGAAA | 9886 |
rs570167136 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917731 | CAACATATGAATTGG[C/G]GGAGGGGGCAGACAT | 9886 |
rs570196187 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874310 | CACTCTTCAGTGCTC[A/G]CTCTTGAACATTCTC | 9886 |
rs570200317 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881178 | TGCCATGTAAGATGT[A/G]CCTTTTGTCTTCCAC | 9886 |
rs570285222 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890168 | AAATGATCCACTTCC[G/T]ACAGCTCTTCTCTGT | 9886 |
rs570288064 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961982 | CTGGATAATTTTTGT[A/G]TTTTTAATAGAGATG | 9886 |
rs570316106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931220 | TCATTCTTTTAAAGT[A/G]TACAATTCAGTGGTG | 9886 |
rs570365347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979421 | CATGGCCTCCATCTC[A/G]TAAGTCTAGCTGTGG | 9886 |
rs570379921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951960 | TTACTCAGGAGGCTG[A/C]GGCAGGAGAATTGCT | 9886 |
rs570494491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996295 | GTTCTTTTTTTTACC[C/T]GCCCAAGCTGATTTA | 9886 |
rs570554041 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887607 | GTGCAGGAAAACTAC[A/T]GAAGTGCAGGGCCAA | 9886 |
rs570569628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917782 | TGTGCCTATACACAC[A/G]CCACTCCTTCTTACC | 9886 |
rs570579844 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944405 | CCTGGTGTGTCTGTG[C/G]TCTGGGACACGGGTG | 9886 |
rs570608609 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987792 | ACCACTTTCCACATA[A/T]CCTTTGCAGACATTC | 9886 |
rs570615192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880778 | TATGAATAATTAATT[A/G]TTCAACTAAATCTAG | 9886 |
rs570635507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905741 | TGCTTGCCATCCTAA[C/T]ATCATCATTACAATG | 9886 |
rs570635539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899546 | GATCATTTGACCATG[A/G]TGACAAAAGGACTCT | 9886 |
rs570640010 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001810 | TGCCTGCGGCCTCGC[C/G]ATTCTCCGCTCAGGG | 9886 |
rs570642807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987243 | CTGAATTTTCTTCTT[C/T]TGGCTTCTCTTCTGC | 9886 |
rs570665800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874898 | TGGAATGTTTTATCA[A/G]CATTAAATGAACTGA | 9886 |
rs570676550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908912 | GAGTGTTCCTGAAGC[C/T]CCTCAATGTTGCTCA | 9886 |
rs570713903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937116 | AGTAGCTTTCTTCCG[C/T]GTATGTGATGAATTG | 9886 |
rs570814146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906874 | GACTGATATGGTTTG[C/G]CTGTGTCCCCACCCA | 9886 |
rs570847788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939041 | TTAACGCTGGGAACT[C/T]GCCATTAACCTGTGT | 9886 |
rs570878883 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990127 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 9886 |
rs570972199 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912247 | CACATATATATATGT[A/T]TATGGAATCTCACGC | 9886 |
rs571007164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959531 | GTGGATGTTGCTCAC[A/G]TGTCTCTGAGCCTGG | 9886 |
rs571026006 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933119 | AGTGCTGGTGGAAAA[C/T]TAACCAGACTTCTTA | 9886 |
rs571065801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877648 | ATACAGCGTGTGCCT[C/T]AAGGGCAGGGGTCAT | 9886 |
rs571108363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941946 | ATACGTTGTTTTCTC[C/T]TTTTCCCCCGAGAAA | 9886 |
rs571111830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960332 | TATTGATTATGCTGG[C/T]GAATTTAATCAAATA | 9886 |
rs571174534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952987 | TAGTTCATTCCTTGG[A/G]ATTTCCTTAACAAAT | 9886 |
rs571201650 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956510 | TTTATTTTGTAAGCT[C/T]AATTTTTAAAAACCT | 9886 |
rs571210534 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998281 | CACACGTGTCTTTTA[A/T]AAGAGATAATTACTT | 9886 |
rs571216125 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949576 | ACTAAAAAGTGATGT[A/C]TTTTTCCTAAAAGCT | 9886 |
rs571242431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992335 | GTGCTAAGATATGAA[A/G]GTAGTATTTTCCAAT | 9886 |
rs571297829 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949398 | TTTTTGCACTTGGGT[A/G]AAAGTGAAAGACCCT | 9886 |
rs571310374 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871302 | TTTGTCCAGGCTCAT[C/T]GATGGTGAGCTTGTG | 9886 |
rs571325316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985398 | TCAGTGCCCAGGCCA[A/G]AAAGGGCGGATGCTC | 9886 |
rs571330101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914362 | GGGTAGTAGCCTGAA[A/T]CAGAAACACAGGTTC | 9886 |
rs571342341 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919289 | TAGTGTATTCAAAGA[A/G]TTAGCCCTGAAATAA | 9886 |
rs571382454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950521 | GAGGGTAACAGAAAG[A/T]GAAAGAAAGCGGTAT | 9886 |
rs571397093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921365 | AGCCCTAAGTTCTCC[A/G]GGAGAGAAAGGATGG | 9886 |
rs571434812 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893891 | AATTATAAACCATCA[C/T]TCTAGGTTAAAATGT | 9886 |
rs571469872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929087 | AGAACTCCAATATGA[C/G]AATAGCAAGGGGGAA | 9886 |
rs571502454 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934817 | CGGAGAGCTGGTGAA[C/T]GTGTATTGTAAAGAG | 9886 |
rs571508024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929760 | AAGGAGAAATTCACA[A/G]CAATAACAAATATAT | 9886 |
rs571508171 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922165 | TCAAGGGATTCTCAG[C/T]GCTTTTTGGTGAGTC | 9886 |
rs571563261 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953481 | AAGTAGTACCTAAGC[A/G]ACTTTTGTCTTAACA | 9886 |
rs571564506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916951 | GGCTTTGAAGATGAA[A/G]GAAGGGGCTGCAAGC | 9886 |
rs571578637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949002 | TAGCAATGAGGTCAG[C/T]CTGGACAGCACAGGT | 9886 |
rs571623045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879720 | ATCTATATATTATGT[A/T]TGATTACATCTTTAT | 9886 |
rs571668425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873366 | AACGCAACAGATTGG[A/G]GTCCCACTTGCCCTC | 9886 |
rs571681918 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979223 | TCATCTGTATCTACC[A/T]TTTTTTGCCTAAGAA | 9886 |
rs571716385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936487 | TACCAGGTCATCACC[A/G]CCTACATCCCTCCTA | 9886 |
rs571717021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891485 | AGCTGAAACCACAGG[G/T]GTGCACCACCAGTCC | 9886 |
rs571744449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986225 | CTGGTGATGCTTCCC[G/T]CATCTTCCAGGTGGA | 9886 |
rs571748551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899054 | GGCCTTGCCAAAGAA[A/G]GTTGTGGGTTATCAT | 9886 |
rs571783661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971263 | GCGAAAAGAACAAAG[A/C]TGGAGGCATCACGCT | 9886 |
rs571802639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921726 | GCTGGCAGAGAACTT[A/G]CATGCAGCTATCTCT | 9886 |
rs571812649 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001007 | ACTGACAGTGACTTT[A/C]TCTCTCTAATCCCTC | 9886 |
rs571867765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977891 | CACTAAAATAAATAT[A/T]CTGCATGATGAAGTT | 9886 |
rs571910733 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887203 | TTACTGTAGGTTTGT[A/G]ACATATTCTTTTCAT | 9886 |
rs571910863 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991689 | ACCCGCCTCAGCCTC[C/T]CAAAGTGCTGGGATT | 9886 |
rs571997851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885655 | GCGGCTTCTCAAGGT[C/T]CCCTGTCTGGTTAGG | 9886 |
rs572053500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898201 | TAATGGGCTTCTTTT[C/T]TTTGTCACTGTGCAT | 9886 |
rs572086620 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962460 | ATGCAAAATAAAGTC[A/G]AAAGTATTTATAAAG | 9886 |
rs572128024 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908919 | CCTGAAGCCCCTCAA[C/T]GTTGCTCAGAGAATC | 9886 |
rs572189836 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, synonymous-codon | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944524 | CCCGGCCCTTTCCCC[C/G]CGCTGCCGGGAGGGG | 9886 |
rs572210886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914860 | TAATCCCTAGCAGTC[C/T]GCTCCAGACCAAAGT | 9886 |
rs572223910 | in-del | -/GTTTTGTTTTGTTTT | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920639 | TTTTTTTTTTTTTAA[-/GTTTTGTTTTGTTTT]GTTTTGTTTTGTTTT | 9886 |
rs572238994 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950313 | TTGAGAGAGAAATTT[A/G]TTTCATGAACTACAT | 9886 |
rs572274605 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981125 | ATTTTTTTGAAATGA[-/G]GTCTAAGATTTTTGT | 9886 |
rs572293264 | in-del | -/TATA | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912203 | ATATATGTGTGTGTG[-/TATA]TATATATATGTGTAT | 9886 |
rs572313169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916793 | TGCAGATGGAATTAA[C/G]GTTGTTAGTCAGCCG | 9886 |
rs572318711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949049 | CTCCAGCTAGTGATG[A/G]CAAACAGGAAAGACT | 9886 |
rs572328709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934718 | GCTCCATGTCCACTG[C/T]GTCTATTATTCTCCC | 9886 |
rs572329570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874894 | ACAATGGAATGTTTT[A/G]TCAGCATTAAATGAA | 9886 |
rs572356934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941968 | CCCGAGAAAGGGAAG[A/G]ATCTGCTTTACTTTT | 9886 |
rs572364414 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874673 | AGAAGGAGGAGAGAC[-/A]AAAACCTCCCCCAAG | 9886 |
rs572399420 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940874 | AATTCAGCCTTCTGG[A/C]AAGTATAATCTTGAT | 9886 |
rs572434476 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879288 | ATCATATTTTATTAA[C/T]GGTTTGTAAGAATTC | 9886 |
rs572475562 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934371 | CAAAGGAACTAATAC[A/C]TCAATAGGCCCAACC | 9886 |
rs572487275 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933649 | GAGGTTGCAGTGAGC[C/T]GAGACCACGCCATTG | 9886 |
rs572526580 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930068 | AATATGAACAAAAAA[A/T]TCTCAACCCTTGGAA | 9886 |
rs572590730 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947487 | TATTTGCACCCCCAA[A/T]CCCCAACCATTAATC | 9886 |
rs572617233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899672 | CTTGCAGAAATAGTA[A/G]TTGAGAACCTACTGT | 9886 |
rs572622487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957323 | TCAGCTTTGTACATT[C/T]GTTTACAGCAGCAGC | 9886 |
rs572625981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940238 | GCACATTAAAAAAGA[A/T]GATATCCTAAGGTTT | 9886 |
rs572638924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872561 | ATGCCTCGCCCTCCC[A/G]CCCTCCCCTGCCACC | 9886 |
rs572667638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964004 | ACCTTTCCCCACTGT[C/T]TCACAACATTCTCTA | 9886 |
rs572670682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949993 | ATTCATTAGGTTTTC[C/T]GTTGGGGTAGGGTGA | 9886 |
rs572690085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999643 | ACAGATTTTCTTCAT[C/T]GTCTGTGAACAAAAC | 9886 |
rs572717713 | in-del | -/CCTGA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981996 | GGCTGGTCTCAAACT[-/CCTGA]CCTCAGGTGATCCAC | 9886 |
rs572751346 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989986 | GAATGTCCTTTTTTT[C/T]TTTTTTTTTTTTTTG | 9886 |
rs572778098 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907062 | CCCTGCACATGCTCT[C/T]TCTCTTGCCTGCCAC | 9886 |
rs572801371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872830 | ATACTCCACCCTTCC[A/G]TTCTAAGCAATGCTC | 9886 |
rs572803558 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882218 | TAAAAAAAAAAAAAG[A/G]GTGATCAAAGAGAAT | 9886 |
rs572860411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901753 | AACTTGTCAAGCTTC[C/T]TGTTATTAAGCAGTA | 9886 |
rs572863152 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870993 | CTTTCACAACAAAAG[A/G]ATAACCCTCTAATTA | 9886 |
rs572863321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876853 | AAATTAATCTTTTAT[C/T]TTTTCTAAAGACATT | 9886 |
rs572873147 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886721 | TTTAAGAGATGTGGG[G/T]GGGGGTGGGTCTGGC | 9886 |
rs572874500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932942 | TTCTGAAGCAGCAGC[A/G]TGACCACCTGCTGTG | 9886 |
rs572894712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982622 | CCAAAACAATCTCCA[A/G]TCATTACCAAATGCC | 9886 |
rs572928879 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873714 | TCCAAGTGTGAACAA[C/T]CAGTTTTGATGGGGG | 9886 |
rs572932339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957139 | CTGAAAGACCAGCCT[A/G]AGGCTGTTTGACACT | 9886 |
rs572958722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912600 | TCTTCTGTGTTTTCA[C/T]CAAGAAATCTGGAAC | 9886 |
rs572981509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960018 | GTAGGCTGGAAATAC[C/T]AATTTGTTCTGACAT | 9886 |
rs573009834 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955148 | TTCCTGGGTTCAAGC[A/G]ATCCTCCTGCTTCAG | 9886 |
rs573020889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902166 | AGGACAGTGTGGGAC[A/G]GCAGGCTGAGGGTGG | 9886 |
rs573021399 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871368 | AGGAAGATCAGTGCC[C/T]GAAACCTGAACTATG | 9886 |
rs573027650 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998170 | ATTATGGTACTCAGA[C/T]CTCCATTCATAATTC | 9886 |
rs573056892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960708 | TTGAAATGATTACAA[C/T]TAGATTGCATTTTCT | 9886 |
rs573073364 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870257 | ACTCAGAATGAGAAA[C/G]AGTCAGAACGAACTC | 9886 |
rs573098104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906648 | TCACCACAAGAGTGA[A/G]GCAGGACAGGACACA | 9886 |
rs573103668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953192 | TAAGGTTAGCCTCCT[C/T]GTGAGTGTATCGTTT | 9886 |
rs573147011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961756 | GATAAGTTATTTTTC[A/T]ATGAATATATTATTG | 9886 |
rs573155812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969323 | ATAGCAGCCACAAAA[C/G]CAACTTTGGTGTTAA | 9886 |
rs573156038 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976053 | CAAGAAATTCTCAGG[C/G]GAAAATGATATATCC | 9886 |
rs573193962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875547 | CTAGACTTTAGACAC[A/G]TTCCTGTTTGACAGT | 9886 |
rs573202115 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995862 | AAAAAAAAAAATCAG[G/T]TTCAAGCAGGTTGCT | 9886 |
rs573260621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955190 | GCTGGGATTACAGGC[A/G]TGCACCACCACTTCC | 9886 |
rs573279563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914458 | CCTTACTCTTTTAAG[A/G]GTGAATTTTTTTTAT | 9886 |
rs573330256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908361 | AAGGTTTCGAATACA[G/T]TTTCAAGAATAGGGA | 9886 |
rs573330699 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999869 | AAATGCCATTTCATA[C/T]ACAGCTTTTTGAAAT | 9886 |
rs573348011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940432 | AAAAGTCTTGCTTAA[C/T]ATTTGGTTGTTATCA | 9886 |
rs573354781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889988 | AAATCCATTCATATA[C/T]ATTTTTCATGTAAGC | 9886 |
rs573363592 | snp | C/T | 3.29908e-05 | 0.00406132 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889131 | TGGTAAGCCAAGTTC[C/T]TTTGCTACCTCTCGG | 9886 |
rs573367483 | in-del | -/TGATG | 0.000450455 | 0.0150008 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911309 | ACTGGCAACCAGCAA[-/TGATG]TGCCCTAGGGATGCT | 9886 |
rs573385018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948584 | GATGCAGCATGTGAT[G/T]CTGTCATTGGCTATT | 9886 |
rs573423040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933960 | ATTGAGATATAGATA[A/T]ACTAAAATATTAATG | 9886 |
rs573453166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883725 | AACATCAGAATAAGT[C/T]CAGCGGCAGCTACTA | 9886 |
rs573479252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926938 | ATGGAAGAAGTCAAA[C/T]TATCCTTGGTTGCAG | 9886 |
rs573491866 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927539 | CAATGGAAGAGAATA[C/G]AGAACCCAGAAAAAA | 9886 |
rs573503967 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951852 | GCCTGAGGTCAGGAG[A/T]TTGAGACCAGCCTGG | 9886 |
rs573512346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883258 | CCAGTTCTAAGTGGT[G/T]AGGGACCTCATCTCT | 9886 |
rs573520748 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891539 | TTTTTCTAGAGACGT[G/T]GTCTCACTATGTTGC | 9886 |
rs573598845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902275 | CAGAATCCCTAAACT[G/T]CCATCACAGATTTAA | 9886 |
rs573612423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975535 | AATGCTACTTATTCG[A/C]TTGCATGGAAATACT | 9886 |
rs573618700 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954475 | TGACAGTTTTATTAT[G/T]TACTCACTGATTGCT | 9886 |
rs573658483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896732 | TCTTCTTTCTAAGGA[G/T]AAAATATCAATATAA | 9886 |
rs573663046 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939294 | TCCATCATTTTTGGC[A/G/T]TCTTTTTGCCAATTT | 9886 |
rs573677009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927033 | AAAGTTTCAGGATAT[G/T]AAATCAGTATACTAA | 9886 |
rs573687062 | snp | C/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917758 | ACATTCACCCTGTAG[C/G/T]ACTATCTCTGTGCCT | 9886 |
rs573692017 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989473 | ATACTTGTTGAATGA[A/G]TAAATGTTTACTCAG | 9886 |
rs573703260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990968 | TTTTCACACACATGT[C/T]CCTCCACCATTGTTC | 9886 |
rs573721388 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921789 | AGCAGCAGCGTGTGG[C/T]TAAGCCTGCAGTTGG | 9886 |
rs573739195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955792 | TGCATCAAACTTGTT[C/T]ACAGCTTGAAAAACC | 9886 |
rs573797355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953288 | GGGGAATAAGCTATA[A/C]ATACAAGACCCCATT | 9886 |
rs573805682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901822 | TAATGTACTGAACAA[C/T]GCATATATTCCTTAT | 9886 |
rs573822804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890127 | TCTATTAAGCAATTA[A/G]AGTCAAGACTTTCCC | 9886 |
rs573840906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991755 | TCTTTCATGCTGCCT[A/G]TTCTGTCTCCTTCTA | 9886 |
rs573848531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954263 | TCTGTAAAATGAAAG[G/T]GCTCTGAGTGGAGTA | 9886 |
rs573873850 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997988 | GCTTCAGTTTGCTCA[A/C/T]CAATAAAACAATGGC | 9886 |
rs573952927 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990710 | GGGCTCATCTTTCAC[A/T]ACTGGGCCATTATGG | 9886 |
rs574001720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963044 | CTACAGATGTGATGG[A/C]AGAATTCTTCCAAGA | 9886 |
rs574031225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903496 | TTACCACCATGTTCA[A/C]CAGTTCCAGAACGAA | 9886 |
rs574055115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874433 | CTTGTGCTTTGGGGA[A/G]GTTACTCCATGGTGA | 9886 |
rs574056807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908496 | CAAACAAGTTTTGCA[A/G]AAACAAAAAAGGTTT | 9886 |
rs574060483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949161 | TCCTAAAATACCTTA[C/T]TGCGTTCAGTCACTC | 9886 |
rs574094824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999422 | GTAGCGTATAAGAAA[C/T]GGGTTTTACTCTAGG | 9886 |
rs574095339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942072 | GGATTTGTGAAAATA[C/T]ATTTTTGAGCTCTTG | 9886 |
rs574136512 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942059 | TTAACATTTTGCAGG[A/G]TTTGTGAAAATATAT | 9886 |
rs574159445 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967542 | GGCAATCCTGATGGA[C/T]GAGAAAAAGAACAGA | 9886 |
rs574171444 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965462 | CAAGTGTGTTTGTAT[G/T]GTTGGTATCATGATT | 9886 |
rs574193806 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982329 | TGTTGACAGTACTCA[C/G]TACGGATACCATTTA | 9886 |
rs574210192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970177 | AATAGTTAATAGCAA[A/C]CTTTCTGTCAATGCT | 9886 |
rs574261485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911860 | CCATTCAGCCACTGT[C/T]GGGACAGCTGGCACA | 9886 |
rs574278276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995743 | TTGTTTCTGCCCTTA[C/T]TGTTTTTTGTTAATG | 9886 |
rs574290848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890520 | CAGTACAGTGCTGGG[G/T]TTATGGCATAACCAT | 9886 |
rs574299549 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909306 | GAATACATTTCATTG[C/T]TGTTGTTTTCTCTTT | 9886 |
rs574299599 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938380 | GGAAGCCTGGGTTCA[A/G]TTCAGACTGTGTCAC | 9886 |
rs574302494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877173 | TGCTTCAGCTTCCCA[A/G]CTGAACAAATCTAGA | 9886 |
rs574345259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973000 | CATGAATCCTTAAAC[A/C]GTGACTATAGAAGTA | 9886 |
rs574347193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965579 | TGTGAGTAATGTGCT[C/T]TTTGATTCTAAGGTA | 9886 |
rs574367197 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958139 | AAGGAGGTAGAAAAG[C/T]CAAGCACCTCTAAAG | 9886 |
rs574389566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873746 | TTGCTGATTCGACTG[C/T]ATTAGATGTCTATTC | 9886 |
rs574393005 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957491 | GTGCAGGACTGTAGT[C/T]TTCTGAGGGACTTAA | 9886 |
rs574424017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914625 | GATAGCAGCCCCCAA[A/G]AAGGAATCCCCCAAA | 9886 |
rs574455037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917917 | CATAAACTAATTTAC[C/T]TTTTTCTCTGTATCA | 9886 |
rs574483577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952432 | TGTTGGGCATGAAGC[C/T]AAATGCTTTTATACT | 9886 |
rs574494141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906105 | AGTGTCTAAGAATAA[A/G]CTAGATAATAAATGG | 9886 |
rs574495082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911789 | CAAACAGTTTATTCC[C/T]GTTAACTGTTATTTT | 9886 |
rs574504363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930817 | GGTTCTTCTTCATCC[C/T]TTCTTACAGGGCTAG | 9886 |
rs574518602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886317 | ATAGCCACCAAACTG[C/T]GACTCCCTTACTCTC | 9886 |
rs574525109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979693 | GAAAGACTGTAACAA[C/T]GAGTGAATTACATCA | 9886 |
rs574550773 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883592 | GCAATCCTCCCAGCT[C/T]TTTATCTCCAGAGAT | 9886 |
rs574591957 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945541 | AGGAAACCGTCTTCA[A/G]TTTCCTGATGAATTA | 9886 |
rs574620800 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976838 | TTAAATTTGAGAGAG[-/A]ATTTCTGGATTCAGA | 9886 |
rs574639419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923590 | TAAAGAGACTGACTG[C/T]CAAAATGCAATCTCT | 9886 |
rs574672736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894377 | TGTATTAATCTGAAT[A/G]TTCAGAATCATCTTG | 9886 |
rs574674034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880841 | TATATGTTTACATAC[A/G]TATGCATTTATCTTA | 9886 |
rs574676834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995710 | AAATCTCAGAAGTAC[A/C]CACAGCATTTTGCTC | 9886 |
rs574693296 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893302 | TCAGTCCTGGAACCA[A/C]AACATGCTGAACTAT | 9886 |
rs574709698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881774 | GCAAAATGAACATCC[C/T]AAATAAAAAGAAACT | 9886 |
rs574738448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973912 | TTTCTCAAAGTAAAG[A/G]TTCTAATGTTTGAAG | 9886 |
rs574809538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974592 | GGGCATGGGATTTGA[A/G]TTTAGACTTGTTTAG | 9886 |
rs574837551 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894838 | CTATTAAGACACATG[C/G]CTCTAAGGGGAATCA | 9886 |
rs574842625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932764 | CCTAAATACACACAA[A/T]AAGATTGAGATAGAG | 9886 |
rs574866756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875682 | CTGTCTCAACAGCTA[C/T]AGATGGATAACATAT | 9886 |
rs574905595 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882504 | ATGTTTTCCTGAATA[A/T]TAAATGACAAAAAAG | 9886 |
rs574918273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967361 | GCAATGGCCCTGTCT[C/T]GGCTCACCGCAATCT | 9886 |
rs574920111 | in-del | -/GTTTT | 0.0134861 | 0.0810011 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920638 | TTTTTTTTTTTTTAA[-/GTTTT]GTTTTGTTTTGTTTT | 9886 |
rs574934235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952526 | GATGAGGAAGCCGAG[A/G]ATCAAAAAGAGCAAG | 9886 |
rs574956360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900858 | CGGCAGAGGTTAACC[A/G]GTTAATCTCTATATA | 9886 |
rs574957042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968251 | TGTCATTTAAAACCA[C/G]AGAAAGATGACATGG | 9886 |
rs574993506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960840 | AATATCCATGAGCTT[G/T]TTATTACCACTTCAG | 9886 |
rs575026664 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879131 | ATTTAAATCTTGTGT[C/T]CAAGGTCACAGAGCT | 9886 |
rs575030509 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926928 | TCAAATTGTAATGGA[A/G]GAAGTCAAATTATCC | 9886 |
rs575036093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988985 | GCTAGGGAAACCTTG[C/T]TTTATTCACATTTCT | 9886 |
rs575080761 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929409 | GAAAGCAACATAAAG[C/T]TGTTCTTAGATATCA | 9886 |
rs575088128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873354 | TAGAAATTGGCAAAC[A/G]CAACAGATTGGGGTC | 9886 |
rs575127766 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000765 | CTCCAAAATACCCCA[C/T]CTCCAGACACCACAA | 9886 |
rs575133296 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945951 | TTGGGAGGCCGAGGC[G/T]CGCGGATCACGAGGT | 9886 |
rs575133322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938096 | TTGGAAGGGTTTATG[A/T]AACAAAGACAGCTTA | 9886 |
rs575231252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975368 | CTCCTTGTCCTATCA[A/G]TTGTTGGAAAGACAC | 9886 |
rs575237062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882580 | ATATGCACATTAATT[A/C]TATTAATTCTCCAAA | 9886 |
rs575257169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938849 | TTTCTTGCCTCTGTA[A/G]AATTGGAATTGATAA | 9886 |
rs575279654 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003240 | CAGCTTCATCCATGT[C/T]CCTGCAAAGGACATG | 9886 |
rs575288049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912547 | CTTAAAAAAGATATT[C/T]TTGAGGGCCCACAAT | 9886 |
rs575294538 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870749 | AATAAGCCCTTCTAA[C/T]GATTATAAAGATTGT | 9886 |
rs575314984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946633 | TGACCTGCTTTTTAA[C/T]AGCCTGCTTTTCCTC | 9886 |
rs575331214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899433 | TGAGGGCAAGTTGCA[C/T]GCATAAGAAAACTTC | 9886 |
rs575345122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973093 | GTATGTCTGTTAATT[A/T]TTTTTTATGATTTTC | 9886 |
rs575352014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918098 | ATACACTGAACGAAT[C/T]ATCAAGTGTTTGTGG | 9886 |
rs575375598 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925276 | TTTATAAATTATTCA[G/T]TCTCAGGTATTTCTT | 9886 |
rs575406991 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923439 | AATTGAAAGCCGTGC[A/T]GGCAACAGTACATAG | 9886 |
rs575411130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981781 | TATAAGTTACTTTTT[G/T]TTTTTAACACGGAGT | 9886 |
rs575414871 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921625 | TGTCACAGTGCCTGG[A/C/T]CTATAGGCAGCTTTC | 9886 |
rs575416330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975821 | AGAAACACTGTAATA[A/G]TGGGTTCTGAGATTA | 9886 |
rs575434361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891148 | GAACAGAAGGATTGT[A/G]AAAACTGAATATAAA | 9886 |
rs575445088 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920737 | TCACTGCAACCCCTA[A/C]CTCCACCTCTCGGCT | 9886 |
rs575454637 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915097 | TGAAATCACAGCCAA[A/G]GATGGAAACTCATGC | 9886 |
rs575455329 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982483 | TTCTCAACCTTGATA[A/C/T]CATTGATTTTGTTGG | 9886 |
rs575469261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967145 | CCTGAACGGTATGCA[C/T]TGGCCCTGTGAAAAT | 9886 |
rs575478014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881101 | AGTGAATAAGTCTCA[C/T]GAGATCTGATGATTT | 9886 |
rs575481269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874565 | ACTCCAGAACAGCTG[C/T]AATGAGATGTTCATT | 9886 |
rs575510367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887192 | CACTGTTTAAGTTAC[C/T]GTAGGTTTGTAACAT | 9886 |
rs575513771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919613 | GAATTCATTGTTGTA[A/G]TCAACATTATTTTTT | 9886 |
rs575514365 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880229 | AGAGAGAGAGAGAGA[C/G]AGAGAGAGAGACAGA | 9886 |
rs575534249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918774 | TTTTTGAGATGGAGT[C/T]TCACTCTTGTTGCCA | 9886 |
rs575579346 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970614 | ATTTTGGACAGTAGC[A/G]TAATTATTTTCGCAT | 9886 |
rs575582599 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946852 | GGGATAAAGAACAGT[C/T]AGCCATGTTGGAATT | 9886 |
rs575608942 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994628 | AAAGATATCCTCAGG[-/A]AAAAAAAATGCAATG | 9886 |
rs575617824 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997729 | AGTAAATGTGTCACC[A/G]AAGTTTATAGAGACC | 9886 |
rs575667200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961630 | GCTCCCCCATCCTCT[C/T]AAATTCTTAGAGATG | 9886 |
rs575719174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897955 | GTGATCTTCCCACCT[C/T]GGCTTTGCAAAGAGC | 9886 |
rs575721825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876142 | CATCTGGGCTTTGCC[A/G]TTTTAAGTAACTGCA | 9886 |
rs575733735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913977 | TCAAAAATTATAATC[A/T]TGATGCTGAAGACGA | 9886 |
rs575748301 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939255 | GGACATCTGGAAAAA[G/T]TGGCAGTCATACTCA | 9886 |
rs575760124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894909 | GTCAATTCTGTTCTC[C/T]AATTTTATGATACAG | 9886 |
rs575771029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895763 | TAACCCTTGTTGATC[C/T]AAATACAAATGCAAG | 9886 |
rs575814967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992509 | ATATTCTGCTGGATA[C/T]GCCTTTTTATATCTT | 9886 |
rs575858556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932198 | ATCTTTACTTAGGCA[A/G]ACGTCTACACATTTT | 9886 |
rs575956907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922326 | ACAAAATGCAATTAG[C/T]TGCACTTCAAGGCAA | 9886 |
rs575960927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878779 | GTCCATATAAATGCA[C/T]GCTGGAGTTCGCCAG | 9886 |
rs575968995 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940243 | TTAAAAAAGATGATA[C/T]CCTAAGGTTTGCTTT | 9886 |
rs575969948 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892065 | AATTTCCTGAGGCCT[C/T]CGCAGCCATGCTAAA | 9886 |
rs575987577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971344 | ACTGGTACCAAAACA[A/G]ATATATAGACCAATG | 9886 |
rs575990382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916161 | ATGTGGTGGAGGTGA[C/T]GCTGTGTGAGGTCTA | 9886 |
rs575993142 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964164 | ATATAACGCATGCAA[A/C]GTTATTTTCTAATAT | 9886 |
rs576033705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925959 | GACATAGTTGGGCGT[A/G]GTGTCTCACACCCGT | 9886 |
rs576045246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873003 | TCTGTTGTCTGTCGC[C/T]CTTGATGTTTCTTTG | 9886 |
rs576053514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922849 | TCAGTTTTGACCCTA[A/T]GATAGAACTGATTGA | 9886 |
rs576064945 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977774 | TTTAAAAATCTCTGA[C/G]TTAATGTTGCATTAA | 9886 |
rs576110247 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942891 | TTTAGAGTATGTTAG[C/T]GCAGAACGTACACCA | 9886 |
rs576117765 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941595 | GGACAAACTGGTTTG[A/G]GGCCCATATTTGTAC | 9886 |
rs576134371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898786 | CTATTTTTTTCCAAG[A/C]CCGTATCTGCATGTT | 9886 |
rs576158183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931358 | CGTTCTCCCCAGCTC[C/T]GGCAACCACGAATCT | 9886 |
rs576173186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904088 | CCACCTCAACCTCCC[A/G]AGTAGCCACAACACC | 9886 |
rs576205404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910606 | CAGCAATCAAAGCAG[C/T]CCGCAGTTGGAGGGT | 9886 |
rs576240021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911196 | AGAGCCACAGTCTCC[A/G]GTTTGCATTTTGCTT | 9886 |
rs576248811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977985 | TATTAAAGGTTGCCT[A/C]ATCTATAAAATGGGA | 9886 |
rs576251600 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939248 | TGTCCTGGGACATCT[A/G]GAAAAAGTGGCAGTC | 9886 |
rs576259726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934802 | GATATCTTGATGAAA[C/T]GGAGAGCTGGTGAAC | 9886 |
rs576301321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946437 | ATGTGGGGGGGCACA[A/G]GGCTGAGTGGCTTAA | 9886 |
rs576326632 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917019 | AAGGCAACAGATTCT[C/T]CCCTAAGGCCCCCAA | 9886 |
rs576372559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899715 | CTTCTAGACATTGGG[C/G]ATAGAGTGATTAGTA | 9886 |
rs576432544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929305 | CATGCATCCATAATA[A/G]TTGAAAATGAAAAAT | 9886 |
rs576446556 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928000 | AAAAAAATCCAATTT[-/A]AAAATGGCAAAGGAA | 9886 |
rs576455257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980102 | TTTATACTTTATTGA[A/G]AAAAGACTATAGGAG | 9886 |
rs576488280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987297 | ACAAGGTTCTCCACT[C/T]GGCAGCAATTTTATT | 9886 |
rs576507386 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923746 | ACTCCATACTGTTCT[C/T]GGGATAGTGACTAAG | 9886 |
rs576550329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000674 | GTATATCTTCATTTT[G/T]TTTTAATTCCCAAGT | 9886 |
rs576557260 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001183 | CCCTGTGCTTTGTCA[C/G]AGCAGCTGGGCTAGC | 9886 |
rs576567732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980694 | TCTCTGGGGAATAAA[A/G]AAAAAGGAAAAACCT | 9886 |
rs576568258 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001122 | CGCTTAGGTAGGAGG[C/G]TGCTCAAGACACCCA | 9886 |
rs576584825 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989345 | TTTGAGATTATCACA[C/T]GAATTTATTTCATTG | 9886 |
rs576606580 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936831 | ATAAAAACTTACATA[A/T]AATCAATTTGAGATT | 9886 |
rs576618989 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950727 | TACCTACTCATAAGT[A/G]TAAAAACGGGCTCAT | 9886 |
rs576619630 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985450 | AAGAGAAATGCCACG[C/T]ACAGCAATCTGGTCA | 9886 |
rs576628997 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899324 | GTGGTAATAAACTCT[C/T]TTTCAACTCCGTCTG | 9886 |
rs576649610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886531 | TTCAAGCATATAAAA[C/G]AGTGGAACGAACAGT | 9886 |
rs576654422 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943897 | GCCACCCGCTGGGGC[C/T]GGGGCGGTGGGGGCT | 9886 |
rs576677445 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957412 | GAATTTTTCAGCTCC[A/G]TTATAATGTTATGGG | 9886 |
rs576688423 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998869 | TCTTAGAGACTGCAA[C/T]GCAGCAGGAAGTACC | 9886 |
rs576696787 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962852 | TGTACACTGACAATA[C/T]TGTGATTTTACTACT | 9886 |
rs576710461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994142 | TATTAATTCAACGAA[C/T]TGACAAAATATTTGT | 9886 |
rs576722045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879396 | CTGTTGCCCAGGCTG[A/G]ACTGCAGTGGCTTGA | 9886 |
rs576760784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964906 | TAATGTAATCCTACC[G/T]TATAGGCAGAAATTA | 9886 |
rs576788795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965546 | CATATTTGTAAGAGA[A/G]TTAATTGGTGTGCCT | 9886 |
rs576807742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957509 | CTGAGGGACTTAAAT[G/T]GTTCCCAGATTGGTG | 9886 |
rs576827524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958006 | AGCAGACACCACTTG[C/T]GAGTGTCTGCCAGAA | 9886 |
rs576876901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923459 | ACAGTACATAGTAGA[C/T]TTGAAAATGTTGTAA | 9886 |
rs576916092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936753 | TTAACAAGATGCCCA[C/T]TTTTGTTGTATGCAC | 9886 |
rs576936526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892680 | CATGATTTATGGGCT[C/G]ACTTAAAACCCATGG | 9886 |
rs576942448 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986728 | ATATAAAAACTGAAG[G/T]GCAAAACAGTACTTT | 9886 |
rs576965845 | in-del | -/AATC | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912166 | ATATTTATTTGTATT[-/AATC]AAATTCATAATTCAT | 9886 |
rs576981453 | in-del | -/TAACTT | 0.00199481 | 0.0315187 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933754 | TTGTGGAAACAAAAA[-/TAACTT]TAGAAGTCCAAACAC | 9886 |
rs576988369 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002288 | CTTTGAATAGTTCAG[A/T]CCTTCCAGTGGTCAA | 9886 |
rs577024714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951555 | ATTAAACACTTCAGG[A/G]TCAGCATCGAAGGTG | 9886 |
rs577044180 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905584 | GAAGGGAAAAAAAAA[A/C]CAAAATAGCAATTGT | 9886 |
rs577067046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929390 | GCCAAATTGATATTT[A/T]TACGAAAGCAACATA | 9886 |
rs577091162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976365 | ACAGAGAGTAAGATC[A/G]CTGAAATCTCCATAT | 9886 |
rs577120899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938638 | AAATACAAAATTTAC[A/G]AAGTAGAAACAAACC | 9886 |
rs577125852 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972699 | TAAAAAAAGAAAAAA[A/G]GAGAGAAAACTAATA | 9886 |
rs577143549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887277 | AGTAAATACTACTCA[C/T]AAGCTTTAAAATGAA | 9886 |
rs577144489 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926386 | CTTATTCTATGAGAC[C/T]AGTGTTATCCTGATA | 9886 |
rs577163431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900280 | ATTAAGAGGTAAGAA[C/T]TCCGAGAGAGAGGAT | 9886 |
rs577180753 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981618 | ATGTATCACATAACC[A/T]ATTAATCAAGATCTC | 9886 |
rs577220712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966500 | CATAGCCAGACCCTA[C/T]CTCTAATTAAAAAAA | 9886 |
rs577238898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922879 | ATCTTCTGGGGTTAA[C/T]CCAAGAAGGAGTCAG | 9886 |
rs577258383 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994779 | AACTATGATGTACCT[C/T]AAACCAATCTTGTAT | 9886 |
rs577258615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931896 | TCAAACAGAAGATGA[A/G]AAATTCTTGGCTTTG | 9886 |
rs577293764 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991785 | AGAGGACTTCCCCAT[A/G]TAGCATGCCTTCTGT | 9886 |
rs577311795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927759 | CTCAAACGATGAAAC[A/G]ATTATAAGAAAATAT | 9886 |
rs577322751 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951862 | AGGAGTTTGAGACCA[G/T]CCTGGTCAACATGAT | 9886 |
rs577331868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994175 | AGTATCTGTGAAATG[C/T]CTGGCACTATAATAG | 9886 |
rs577348037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911717 | GCCTAATTGACACTC[A/G]AGTTTTCTTTTTATA | 9886 |
rs577367122 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994894 | GGCACCAATCACCCT[C/G]TCACAGTTGAAGATA | 9886 |
rs577368870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987496 | AGATTATGGCCACCT[C/T]GCATACAAAAAGCCC | 9886 |
rs577371282 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903521 | AACGAACCAGCTACA[A/G]AAGACAAAATTGTTA | 9886 |
rs577393714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907662 | ATACTTTTTTTTGGA[G/T]AGATGGATGATTTCC | 9886 |
rs577394593 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898586 | TGGAGAGGCCTGTAG[A/G]GGAGCGCCTGGCAGG | 9886 |
rs577400843 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902509 | CTATAATTGGAAAAG[C/G]GTTATTATTCATACA | 9886 |
rs577415224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881712 | TCAGATTACCTTAGC[A/G]TTTTTTGGCAAGAGT | 9886 |
rs577489421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938010 | TATTTCACCGAAGTT[A/G]CATAGTTAATGAAAT | 9886 |
rs577517185 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950781 | GTGCAGCATAGGGTA[G/T]CATTTGATTTAGGAG | 9886 |
rs577539089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890556 | AGGCATAGATGGGTT[C/T]CAGAACACAGGCAGG | 9886 |
rs577564766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902955 | GACAAAATCTCTGTC[C/T]TAAATATACTAGGAT | 9886 |
rs577642970 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990880 | CACCCATAATCCAAT[A/G]TCTGTCTGCTGTCTC | 9886 |
rs577652760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934658 | TCCTTTACTTGAAGC[C/G]TCTTTCCAGGAGCCT | 9886 |
rs577695456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921029 | ATGATAGCTCACTGC[A/G]ACCTCTGCCTCCTGG | 9886 |
rs577699949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891419 | AATCATGGCCCACTG[C/T]AGCCTTGTCCTCCCA | 9886 |
rs577728321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984826 | AACATTTATTTTCAG[A/T]CTTATGTACACATTT | 9886 |
rs577732865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997454 | TAAACTTTAAGAACT[C/G]TTTGTTTATAAAATG | 9886 |
rs577761560 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886610 | ACGTATATTTTTAAT[C/T]TACACCATTTTACTT | 9886 |
rs577765544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977043 | TTGAGATCTGTAAAT[G/T]AAGGAGAATTATATA | 9886 |
rs577793860 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000115 | ACTCAGGAAGCATTT[C/T]ACAAATCTTTTATTA | 9886 |
rs577808801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877326 | TTACTATGTGCCAGA[C/T]GCTGTTCTAAGGACT | 9886 |
rs577810459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884415 | CTACTTTTTTAAAAA[A/G]GATGTTAAAAATACT | 9886 |
rs577824804 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893230 | ACTGCAGAATGCTGA[C/T]GCATTGACGTTTCCG | 9886 |
rs577832318 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970073 | AGTGCACTCTCCAGT[A/T]GTATCTGGTCAGGGC | 9886 |
rs577837807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940498 | ATCCATCTACGTGGT[G/T]CCTTTCAGACAAACT | 9886 |
rs577868834 | in-del | -/ATG | 0.00119737 | 0.0244387 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967748 | CTTTATTCCTTAGAA[-/ATG]ATTGCAACCCCAGGG | 9886 |
rs577881873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941106 | GTTATTATATGTGCT[A/G]GTAATTACCAAGCTA | 9886 |
rs577886129 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919297 | TCAAAGAGTTAGCCC[G/T]GAAATAAAAAACTGA | 9886 |
rs577891882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955892 | TTGTTACATTTATAA[A/C]AACTTTTAATTATTA | 9886 |
rs577907063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896914 | ATCCAAAAATGCCTG[A/C]GCTGATAAAGCCAAG | 9886 |
rs577916639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956585 | TTAGCTGTACAAAAA[C/T]ATCTTCTTTATATCC | 9886 |
rs577918311 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949327 | AACCTACCATCACTA[A/T]CCCTTTCTGTCCCAA | 9886 |
rs577922781 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967474 | TTGTTTGCTTTTCAG[A/G]TTCAAGGAACACATT | 9886 |
rs577982697 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948438 | GAGACCTTAGCCACG[G/T]GTAGTCGAGGCTGAG | 9886 |
rs578032052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942962 | TCTCAAGCTGAGCGT[C/T]TGGCTGGAGTTCAAC | 9886 |
rs578045458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943754 | CTCCTAGAAATCTCT[C/T]GTGCTTGCCTCTGAT | 9886 |
rs578059215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904160 | CCATGTTGGCCAGGC[C/T]GATCTCAAACACCTG | 9886 |
rs578068513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993434 | AGTTTCTATTATATA[C/T]ATATGCATATATTCA | 9886 |
rs578086416 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903653 | ACATAACCACAGGCT[A/G]AGAAACAGGCCCCTG | 9886 |
rs578091674 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918425 | GCGCATGCCCACTCC[C/G]TCACTCACAAGACAC | 9886 |
rs578108824 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946677 | TCTCAGTTCTAAGTT[-/A]AAAAAAAGTTCAGTG | 9886 |
rs578127178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915213 | TTTTATCCTTCTCCG[C/T]TTGTTATAGGCTCTA | 9886 |
rs578186984 | snp | A/C | 1.68203e-05 | 0.00289998 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878072 | ACCTGAAATGTTATA[A/C]AAAAAGCTAAATTCT | 9886 |
rs578225945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909092 | GGGAGGGAACACACA[C/T]GCAGGTATGGCATGT | 9886 |
rs578257442 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998859 | TGTGAACTCTTCTTA[C/G]AGACTGCAACGCAGC | 9886 |
rs745328392 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931653 | TACACTTATACAACC[C/T]AATAATAATACATGA | 9886 |
rs745336339 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919183 | GCTATTGCACGGACA[C/T]TACATTTTCTTATTC | 9886 |
rs745343004 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972806 | CAAGCTTAATCTAAC[C/T]ACTGCTAAATCTTCC | 9886 |
rs745351431 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990038 | CCTAGGCTGGAGTGC[A/G]GTGGCGCGATCTCGG | 9886 |
rs745371632 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943227 | AGTCTAAATATTGAC[A/G]TCGCTCCTCAGTTGA | 9886 |
rs745382566 | snp | A/G | 1.74845e-05 | 0.00295668 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888199 | TAATGGCTCTGCCCC[A/G]CGGCCCACTCACCCG | 9886 |
rs745383591 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930780 | CTTTCTGCCTCTCAG[A/G]ACCTGGGATCTCTTC | 9886 |
rs745434857 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893810 | AGGAGTCAAAGAACT[A/G]TTTTACAAAACAGTT | 9886 |
rs745440397 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965617 | AAGTGCCTCCATGTT[C/T]GACACAAAATAGGTC | 9886 |
rs745459906 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872209 | TTGATTTGATTTCCT[G/T]ACGGAACTTGGAGCA | 9886 |
rs745474118 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870836 | TGGCACATATAACCA[C/T]ATAATTACCAGCACT | 9886 |
rs745475913 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967305 | TTTTTTTTTTTTTTT[-/C]TTTTTTAGACAGAGT | 9886 |
rs745511827 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886523 | TGCAAAACTTCAAGC[A/G]TATAAAACAGTGGAA | 9886 |
rs745517342 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942374 | GATCACAGAGCCTGT[A/G]TTATGCACTTAAAAA | 9886 |
rs745520342 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882309 | GAAGATTAGCTGAGA[C/G]TATTAGGCTTATAAT | 9886 |
rs745523145 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908318 | CTTCTCTCACTGTCA[C/T]CACAAGAATCAAATT | 9886 |
rs745556636 | snp | A/C/G | 3.29789e-05 | 0.00406061 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888298 | TCCTGGTTCATGAAG[A/C/G]CTTCCTTGTTCATGA | 9886 |
rs745586017 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897739 | TGAGATGGAGTCTTG[C/T]TCTGTTGCCCAGGCT | 9886 |
rs745598604 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961298 | TAGAGCTGGACACAT[C/T]TGGATTAGAACCCTG | 9886 |
rs745605024 | snp | A/C | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912531 | AGCCACCATGCCTAG[A/C]CTTAAAAAAGATATT | 9886 |
rs745643616 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952964 | GGGAAAACACACAAC[A/G]CAAGCTTTAGTTCAT | 9886 |
rs745702674 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898997 | TTGAGTCTTAGAAAT[G/T]GTTGGTTCTACCATC | 9886 |
rs745776554 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928463 | TAAGAAATCCTGTTG[-/T]TTGAAACAACATGGA | 9886 |
rs745827885 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913614 | TCTGGAAACGTGTCT[A/G]GTTGTCACTTGGTGG | 9886 |
rs745862226 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888881 | CATCGGCACATAGAG[A/G]ATTGTCCAGTAAACA | 9886 |
rs745865542 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984293 | TCAGCATAGTAATCA[A/C]CATTACAAATAGGAA | 9886 |
rs745872366 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941970 | CGAGAAAGGGAAGAA[C/T]CTGCTTTACTTTTGC | 9886 |
rs745880719 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971872 | AACCCCATCAAAAAC[A/T]GGGAAAAGGATATGA | 9886 |
rs745905344 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916767 | CATTGTGTGGCATGA[C/G]GGAATAGGGTTGCAG | 9886 |
rs745907945 | in-del | -/AT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955939 | CATTGAACTACTATC[-/AT]GTGGTATTCTGCAAA | 9886 |
rs745908792 | snp | A/T | 8.47135e-05 | 0.00650765 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911036 | GGTGTCAGTCAGAAG[A/T]TCCCCAGGAGAAGCG | 9886 |
rs745914485 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957643 | GTGCTAAAAAGCAGA[C/T]CCAAGTGAGTAAGTA | 9886 |
rs745966408 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956467 | TTCTTTCTTCATTAA[C/T]AAATTAATCTTAGGT | 9886 |
rs745988986 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939027 | AGATCATAACCTCAT[G/T]AACGCTGGGAACTTG | 9886 |
rs746015218 | in-del | -/TAGGTAGACC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880437 | GAATATCCTTTCAGA[-/TAGGTAGACC]CATCCCTTAACGTAT | 9886 |
rs746026554 | snp | C/T | 8.25757e-05 | 0.00642503 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875014 | GCCACTCGTGGCGGC[C/T]TTGGTCAACTCCTGA | 9886 |
rs746041419 | snp | G/T | 1.6836e-05 | 0.00290133 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888617 | CCTCCACCAGGCTCT[G/T]GTTTGAAGACTTCCA | 9886 |
rs746116673 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998578 | TCCTAGAGGAAGTGC[A/C]ATTTACTTAGACCTA | 9886 |
rs746149793 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909995 | CTTCAGAAATGCTTA[C/T]CTCAATACCAAGGAG | 9886 |
rs746158475 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933655 | GCAGTGAGCCGAGAC[C/T]ACGCCATTGCACTCC | 9886 |
rs746180697 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992261 | AATGGGAATAATAGG[G/T]GTTTTTGAATGAAAC | 9886 |
rs746196869 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924431 | GGTCATTATATAATG[-/A]CAAAGGGGTCAATTA | 9886 |
rs746205944 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897872 | ACCATGCCTGGCTAA[-/T]TTTTTGTATTTTTAG | 9886 |
rs746209830 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980118 | AAAAGACTATAGGAG[A/G]CAAGGGTGGAAGCAA | 9886 |
rs746235254 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980994 | ATATTAAAATATGCT[A/G]GAAAGATGTGTACAT | 9886 |
rs746249294 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967508 | CCCTCAAAAAACAGA[A/C]CGGCAGCTGAGAGAG | 9886 |
rs746284601 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985691 | ATTGAACTAAAAAAC[A/G]AAATATTTCTATTTT | 9886 |
rs746346041 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889416 | CACATAATTTGTGAA[C/G]CTTATCCATAAATAT | 9886 |
rs746376760 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905012 | CATGCATTGCTAACT[G/T]TCTTCCCTTAGTTAC | 9886 |
rs746377932 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959619 | AGTCCTACAGTGATG[G/T]CTCTGGCAATAAAAC | 9886 |
rs746409143 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927006 | AAAAAACTATCAGAA[C/T]TGATAAATAGTAAAG | 9886 |
rs746449733 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921354 | AATGGTGAGGAAGCC[C/T]TAAGTTCTCCAGGAG | 9886 |
rs746451586 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886958 | AATAACAACAGTCTC[C/T]TAAATAACCATACTA | 9886 |
rs746470404 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968239 | AAACCCAGAGAATGT[C/T]ATTTAAAACCACAGA | 9886 |
rs746490505 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962459 | AATGCAAAATAAAGT[C/T]GAAAGTATTTATAAA | 9886 |
rs746508525 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966206 | GTTTTCTCTGATGTT[-/A]AGGATTATGAGTAAT | 9886 |
rs746517061 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872212 | ATTTGATTTCCTTAC[A/G]GAACTTGGAGCATAC | 9886 |
rs746523297 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961729 | CTTTCACAAGCTATA[C/T]ATTCTAAGGAAGATA | 9886 |
rs746641662 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900112 | AGGGGAAACTGAAGT[A/C]TTTGAGCAGAACGTA | 9886 |
rs746660825 | snp | A/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884709 | GAACCTAAAGGATAT[A/T]ATGTTAAGTGAAATA | 9886 |
rs746690836 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910054 | ATAAAATCCTGTAAG[A/G]TGATATGATGTTTGA | 9886 |
rs746710873 | in-del | -/TTAATTAATGA | 0.000685118 | 0.0184957 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888197 | TTAATGGCTCTGCCC[-/TTAATTAATGA]CGCGGCCCACTCACC | 9886 |
rs746715482 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903406 | AGAGGACCCACTTGA[A/T]CACTCAACTCGGCAC | 9886 |
rs746731245 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950983 | CTCCCATCTGTACAA[A/G]TTAGCTAAACTACAT | 9886 |
rs746737231 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981097 | TGTAAGTTTTCTTTT[G/T]TCTTCAGAAATGAAT | 9886 |
rs746746166 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929918 | ACAGCTTTCTTTCAA[-/G]TGTTCTTGGCACATT | 9886 |
rs746753005 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953674 | CTGTTATTACAGTGA[A/T]AACAGAATAGTCTAG | 9886 |
rs746764658 | snp | A/T | 1.65971e-05 | 0.00288067 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886089 | TCATAAAGACACCAC[A/T]ATGCTTTTAGGAAGG | 9886 |
rs746783794 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889007 | TCTGGACTTTCTTTA[A/G]GTGGGATTTCCAGAA | 9886 |
rs746783934 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998425 | TTCTGATGGGGAAGT[A/G]AGGAGTGATGGGGAA | 9886 |
rs746876153 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937756 | AAGGTTCCTATAACC[-/A]TTCCTTAAAATATCA | 9886 |
rs746882691 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990141 | GCGCCCGCCACCACG[C/T]CTGGATAATTTTTTG | 9886 |
rs746902854 | snp | A/G | 3.29859e-05 | 0.00406102 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910903 | TGCCATATGCAAAGC[A/G]TCTGTCTTTGTGATG | 9886 |
rs746910128 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895445 | GTTTTGCTCTTGTTG[C/T]CCAGGCTGGAGTGCA | 9886 |
rs746956330 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911142 | TAAGTCTTAATTCCC[A/T]TCCTGGAATCATCTG | 9886 |
rs746961633 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894029 | TACAATTTCATTAGA[C/T]GTTAATTTATTGCCA | 9886 |
rs746972328 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992289 | AACATTTCACCTGAG[A/C]AGATGTAACTGGTTT | 9886 |
rs747017003 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974177 | CACCCCTCTTTCCAG[A/C]AGTTTCAAATACATA | 9886 |
rs747040104 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906493 | CACAAACTACAACAG[C/T]ATGGTGGATGGGGAA | 9886 |
rs747044660 | snp | A/G | 1.67469e-05 | 0.00289364 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888656 | CCTGAGGAATCCTAG[A/G]CGGGCCCTCCTCCCT | 9886 |
rs747066744 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934597 | TAGAATCTGATATAA[C/T]GGTTCATTGTTGACT | 9886 |
rs747074951 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988142 | GATTTCACTGTGTTA[A/G]CCAGGATGGTCTCGA | 9886 |
rs747076036 | snp | A/C | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60868944 | CACTCAGAAAAGTCC[A/C]TCAATGACATCTCAC | 9886 |
rs747087274 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998783 | CCCAGAGGGTTTAAA[G/T]GACTTCTCTGAGGTC | 9886 |
rs747100686 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976924 | GCTCAGCTAACAAGC[C/G]AATCTTTAGACTTTA | 9886 |
rs747104918 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946726 | ATAGGCAGGTGCCTA[C/T]ACCAGAAAGACACAC | 9886 |
rs747134010 | in-del | -/GTTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920643 | TTTTTTTTAAGTTTT[-/GTTTT]GTTTTGTTTTGTTTT | 9886 |
rs747144106 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919457 | GAGCTGTTTCATACA[C/T]AAAATAAACATCTCA | 9886 |
rs747159516 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964289 | TGGAGAGAAGGTTGG[C/T]GCCAGAGAGGATACA | 9886 |
rs747239370 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951657 | GGTATCCATCTTAGA[A/G]GAGCTTGAAGATTTG | 9886 |
rs747241044 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935535 | TACTAAAACTGTGGG[C/G]TCTAAGTTCTTTGAG | 9886 |
rs747270780 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869909 | TGCCAGTAATAAATG[C/T]CCATCTGTAATCTAG | 9886 |
rs747295434 | snp | C/T | 1.65919e-05 | 0.00288022 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888713 | TCCGCCCCTGGAAAT[C/T]TCTGCTCTGCTTCTC | 9886 |
rs747301764 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923003 | TCAACTCACATTATA[C/T]TGAGTAGCTTTGCTT | 9886 |
rs747304959 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978472 | TATTCTACATTATAG[A/G]CTGAGATAAAGAATT | 9886 |
rs747306193 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982227 | AGTGGGTCACTCTAC[C/T]CCTAAAGGCACCTAT | 9886 |
rs747331667 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928267 | TATATGGATGTTCCT[C/T]AAAAACTAAAAATCA | 9886 |
rs747357520 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970071 | CCAGTGCACTCTCCA[G/T]TTGTATCTGGTCAGG | 9886 |
rs747371169 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969162 | AATTTAATGAGGTAA[C/T]ATTAATGGAAATAGA | 9886 |
rs747388606 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956937 | ACCCATATGTGCATC[-/A]AACTTGTTTACAGCT | 9886 |
rs747400923 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880422 | GACACCTCAGAGAGG[A/G]AATATCCTTTCAGAT | 9886 |
rs747440270 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900777 | AAGAATGAAAATATA[A/G]TGTGAGCCATTACAG | 9886 |
rs747455774 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888313 | GCTTCCTTGTTCATG[A/G]TGTTTTCCACCATCA | 9886 |
rs747455926 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905967 | GGGGTGTGTTCATTC[A/G]TGTCTGATTACAGGT | 9886 |
rs747467849 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000362 | GTAATAAAAAATATA[C/T]ATTTTGGGTTTTTTC | 9886 |
rs747472800 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889672 | AAAAATGCTGTCAGC[C/T]GTAACCACAGTAACT | 9886 |
rs747494660 | snp | A/G | 3.40304e-05 | 0.00412481 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893011 | CTAAAAGGAAATCAT[A/G]AAAGAAGCTTGTATT | 9886 |
rs747521104 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987073 | TGCACAGCCCATTTC[A/G]TGGGGCTGTGCCACA | 9886 |
rs747574035 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994401 | TCTTATCTGGGCCAA[A/G]CACCATCTGAGGGAA | 9886 |
rs747579850 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957758 | GTCCAATGGTAATGA[C/T]ATTTATTGAATGCTC | 9886 |
rs747599944 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002020 | GGGTTCTGCTGACAT[C/T]ACAAATCACACATGG | 9886 |
rs747614434 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973431 | TAAACTGTATTTGAG[A/C]CTTCTTAACAGCCTT | 9886 |
rs747620603 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951648 | TCCTGTCACGGTATC[C/T]ATCTTAGAAGAGCTT | 9886 |
rs747623682 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981199 | AAAGTACTTAACATC[A/G]TAGTTATCATTCTTT | 9886 |
rs747672978 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982341 | TCAGTACGGATACCA[C/T]TTAGGTGATGTGGAG | 9886 |
rs747711534 | in-del | -/GGCACATTTTCA | 1.71982e-05 | 0.00293237 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878108 | AGAAAGCAGGGAGTG[-/GGCACATTTTCA]GGCTATGCTGCTTAT | 9886 |
rs747743668 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886163 | CATGGCTGCCATCCA[C/T]TCACAGCTACAGATC | 9886 |
rs747745633 | snp | C/T | 3.31614e-05 | 0.00407181 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889155 | CTCTCGGCCTTTTTC[C/T]GGGGGCAAAATATCC | 9886 |
rs747755453 | in-del | -/G | 6.8011e-05 | 0.00583103 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871456 | TACCGATTGGTTTCT[-/G]TTTTTTGTTTTTTTT | 9886 |
rs747777626 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901870 | GTGGCCTCATTAATC[A/G]CACTCCTGTGGACTC | 9886 |
rs747779666 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890971 | CCCCTCCACTGTTCT[C/T]TATAGCTCTGCAACT | 9886 |
rs747808434 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928319 | TCCCACTGATGGGTA[C/T]ATATCCAAAACAAAA | 9886 |
rs747813521 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874177 | CCAAACCCAACAGGC[C/G]GAAGAAAAGACTGAG | 9886 |
rs747826131 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926125 | GCTACTAATCTCAGC[C/T]ACTCGGGAGGCTGAG | 9886 |
rs747833492 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889033 | CAGAATTGCAGGTGC[C/T]TGCGGGAAATCAGCG | 9886 |
rs747858742 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985957 | AAACCTAGGAAAGAG[A/T]TATATACAAGCATGG | 9886 |
rs747874618 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982922 | TGGTGGGCATGGAGC[A/T]GTGGGAGGGAAAGGC | 9886 |
rs747876571 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970418 | TATTAATAATAACAT[G/T]CATTTTTCCTTTTTA | 9886 |
rs747910063 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905583 | AGAAGGGAAAAAAAA[A/C]CCAAAATAGCAATTG | 9886 |
rs747916276 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992582 | TGCTTCCATATGGTG[A/G]CAGAATTCTAGCAAC | 9886 |
rs747943079 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986871 | ATCCAGCTCTCCTCC[C/T]TTTCTGTGCCTCTCT | 9886 |
rs747950824 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886216 | TGGCTCCATCGTCCA[A/G]TTTAAATGTCACGTC | 9886 |
rs747962928 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932044 | GCTTAGATCAATATA[C/G]CATAATTCAGTTTTA | 9886 |
rs747964975 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945310 | ATAAACCTTTATTGA[A/G]TAGGCTGTGTGCAGA | 9886 |
rs748021475 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911431 | ACTGCGTGAGTGTGG[C/T]GTTGCACGCCCTGGC | 9886 |
rs748022002 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922600 | TCTTCACCACAGATG[C/G]CCATAATCTGGAGTA | 9886 |
rs748102715 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910302 | CTAGAGGAGTTTTCC[C/T]ATTACTAGATTTTTT | 9886 |
rs748122402 | snp | G/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883641 | ACCAACTGGATGAGG[G/T]TTTACAAATTGGTGG | 9886 |
rs748138665 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934355 | CTCCCTTTACTTATA[C/T]CAAAGGAACTAATAC | 9886 |
rs748152027 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962857 | ACTGACAATACTGTG[A/G]TTTTACTACTTTAAC | 9886 |
rs748157818 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921524 | TAATACTGATTATTA[A/T]GTTTATATGCATTCC | 9886 |
rs748163791 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871541 | TTGAGCGATGCTTAT[C/T]TAGTGCAATATCTTC | 9886 |
rs748180516 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924577 | TCCCACCTTCAGCAT[C/T]GGAAAGATCATCTAG | 9886 |
rs748223686 | snp | A/C | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877989 | GATCCAAGTTAGGAG[A/C]CAACTGCTTGGTATA | 9886 |
rs748225336 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979992 | GGGAGAGGGAGGAAC[C/T]GGAAGGAAGTGAGGT | 9886 |
rs748230289 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982405 | TATACTAAGATTTTT[G/T]AGGGTGTATTGTGTA | 9886 |
rs748264185 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949084 | GTTCTGAGGCTCTTC[A/G]TTAATGCTAAGTATT | 9886 |
rs748291452 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887838 | AACAAGCCCACTGGA[G/T]ATAGGCTTGGGGTCC | 9886 |
rs748296679 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870422 | TACTTCTGCAGCAAC[A/G]TGAATTTTCCCTGGG | 9886 |
rs748323687 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941670 | TATGACATTCATAAC[-/T]TGAGTCCATAAAAAA | 9886 |
rs748345620 | snp | C/T | 1.7249e-05 | 0.0029367 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893019 | AAATCATAAAAGAAG[C/T]TTGTATTGCCTTTTA | 9886 |
rs748364514 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875164 | ACACAGCTCTGGGCA[A/G]GCATCTGAATTAAAT | 9886 |
rs748371474 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997670 | AAATAGAATTGGTAA[A/G]CTAATGATAAGTATT | 9886 |
rs748385740 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966601 | GTAGCTCTGCTTTAC[A/G]TAATCTTTAAACCAT | 9886 |
rs748412976 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886728 | GATGTGGGGGGGGGT[G/T]GGTCTGGCTATGTTG | 9886 |
rs748419771 | snp | C/T | 1.66763e-05 | 0.00288753 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886067 | AAATACACAGGCACA[C/T]ATACATTCATAAAGA | 9886 |
rs748471689 | in-del | -/TTTT/TTTTT/TTTTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955043 | TCTTTTCTTTCTTTC[-/TTTT/TTTTT/TTTTTT]TTTTTTTTTTTTTTT | 9886 |
rs748519873 | snp | G/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003364 | TTGCTATTGTGAATA[G/T]TGCCGCAATAAACAT | 9886 |
rs748531794 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888344 | TCCTCAAATCGAACA[C/T]CTCGAGGACCTCTGC | 9886 |
rs748577709 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897984 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 9886 |
rs748581344 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892303 | TTGCAACTATAGGTC[C/T]GAATGATTTTCAAAA | 9886 |
rs748643393 | snp | A/G | 3.29674e-05 | 0.00405988 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888411 | ATCCAGTTGTCCCGT[A/G]TAAAGAAACTGGAGC | 9886 |
rs748661716 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947982 | CATTTGTATTATCAT[C/T]ATTGTTTACAAAGTT | 9886 |
rs748697543 | snp | C/G | | | utr-variant-5-prime, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944079 | CGGTCGCGGGTGTGC[C/G]GGGCCCCTGCGCGCG | 9886 |
rs748706439 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929674 | TACAAAAGGCCAATT[A/C]ATAATAGAAGTAACA | 9886 |
rs748712673 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982952 | CGGTGCACATGACAT[A/G]AGGCACAGAACTTTT | 9886 |
rs748744650 | in-del | -/AACACA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926731 | GAAGGAACATATCTC[-/AACACA]ATAAAAGCAATATAC | 9886 |
rs748819845 | snp | C/T | 1.68352e-05 | 0.00290126 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889174 | GGCAAAATATCCCCT[C/T]TCTTTATGGGCCTGA | 9886 |
rs748832680 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929386 | TTGGGCCAAATTGAT[A/G]TTTATACGAAAGCAA | 9886 |
rs748847305 | snp | C/T | 1.78159e-05 | 0.00298457 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888187 | AATCAAAGGTATTAA[C/T]GGCTCTGCCCCGCGG | 9886 |
rs748886144 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002308 | CCAGTGGTCAAGATG[A/G]TCTAGGCCAATCACT | 9886 |
rs748910236 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880808 | GCACCAGTTACACTG[C/T]GTGTATGCTCGCATA | 9886 |
rs748939630 | snp | G/T | 3.32265e-05 | 0.0040758 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892832 | ACGGGCGCCTGGCTC[G/T]ATTAACAGCTTCCAG | 9886 |
rs748958607 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989764 | CAGACATGTGCTCTG[C/T]GATGTCCTAGGCTCC | 9886 |
rs748989885 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930614 | AAACACAAACTGATT[A/C]TTGGAAAGCTGTGAA | 9886 |
rs749006790 | snp | C/T | 0.000164715 | 0.0090736 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911459 | GGCACAGATCAAGCG[C/T]GTCTTCCCCACGGCA | 9886 |
rs749041578 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934498 | AATCTTTCCAGATCA[A/G]GACATGAGACTTTGA | 9886 |
rs749042013 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922862 | TATGATAGAACTGAT[A/T]GATCTTCTGGGGTTA | 9886 |
rs749050674 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915216 | TATCCTTCTCCGCTT[G/T]TTATAGGCTCTAATT | 9886 |
rs749053687 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951365 | AGCAAAGATGACCTC[A/C]CTTCTTGCGCCTGAC | 9886 |
rs749064976 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976541 | GAAGTCTGAAACAAA[C/T]ATTTCAGTGACATTC | 9886 |
rs749082700 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964115 | AAAATATAATCTTAG[C/G]AAAATGAGATTTTTC | 9886 |
rs749104461 | snp | A/G | 1.98143e-05 | 0.0031475 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871675 | GGAAAGATGCAGACC[A/G]TAAGACCTGCGGTTC | 9886 |
rs749109387 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994473 | CTATGGGAGAAACAG[C/G]CTTGTGAAAATGATA | 9886 |
rs749166915 | snp | C/G | 1.65781e-05 | 0.00287902 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888728 | CTCTGCTCTGCTTCT[C/G]TTTCTCACAGGCTCC | 9886 |
rs749178210 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973951 | GCCAAATAGTTTACC[C/T]GAAGATGGAAGAATG | 9886 |
rs749200562 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874242 | ATTGTTAATCAGCCT[C/G]TGCCAGGGACTAGAT | 9886 |
rs749228527 | snp | A/C | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912297 | CAAGCACAGTGGTGC[A/C]ATCTCCACTCACTGC | 9886 |
rs749262131 | snp | A/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885531 | TCATATCCCCTCAAC[A/T]CAGGCAGAGTCAGGG | 9886 |
rs749279911 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911396 | CCACACTGTTGGCAC[A/G]TGGGTGGCCAGCAGC | 9886 |
rs749304844 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982398 | ACATAATTATACTAA[G/T]ATTTTTGAGGGTGTA | 9886 |
rs749317948 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926592 | TATGCAAATCAATAA[A/G]TGTGACACATCATCT | 9886 |
rs749359306 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954974 | AATTATGCATTTATA[A/G]GAGGGAAATAGTCCA | 9886 |
rs749380418 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998549 | GAAGAACAGAAAGGT[G/T]TTCAGAAGAAGACTC | 9886 |
rs749389664 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937678 | TGTGAAGAAAACAAG[G/T]GTAATGGAGACTGGG | 9886 |
rs749401744 | in-del | -/TTTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949665 | GTTTCCAGGTGAAGC[-/TTTTT]TTTTTTTTTTTTTTT | 9886 |
rs749420885 | snp | A/T | 1.65886e-05 | 0.00287993 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878046 | ATATCTTGTTTATGT[A/T]CGGGAGATACACCTG | 9886 |
rs749447124 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935191 | GCTGCATACATTATG[A/G]ATGAATCTCACAAAC | 9886 |
rs749459639 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904665 | GGGGCCAGAGGACCA[C/T]CTGCCTCAGAGTCTT | 9886 |
rs749464528 | snp | C/T | 0.000115423 | 0.00759593 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888433 | AACTGGAGCAGGGTC[C/T]GAAAAGGGCCTGGCT | 9886 |
rs749482193 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937295 | ATGGGGAAATTGTGG[C/T]GTTTATGCTTTTCCT | 9886 |
rs749528547 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876771 | TATCTAACTGGGGAG[A/G]AAGTAGGACAAAGAG | 9886 |
rs749533286 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956059 | TTAGGCAATTTCATC[A/G]TTGTGCAAACATCAT | 9886 |
rs749541978 | snp | C/T | 4.95086e-05 | 0.00497512 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910895 | GGTTTACCTGCCATA[C/T]GCAAAGCGTCTGTCT | 9886 |
rs749559816 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920275 | AAGAAACAAGTAAAC[A/G]GGTAGACAAATACAT | 9886 |
rs749612834 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989391 | TGGTAGATTTTCCAT[C/G]AGGGACGGAAAATGT | 9886 |
rs749618856 | snp | A/C | | | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944508 | ACAGAGCATGGGAGA[A/C]CCCGGCCCTTTCCCC | 9886 |
rs749642545 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001758 | GTGGGGCTCCTACTG[A/G]GACCCCGGTCTTTGG | 9886 |
rs749660433 | snp | A/G | 1.65778e-05 | 0.002879 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874929 | TTGAACACACTTAAA[A/G]GGTAAAAAGCAAACT | 9886 |
rs749667833 | snp | G/T | 1.66902e-05 | 0.00288874 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888541 | ATGCCAATGAACCCC[G/T]TACTCCATCCGGTCA | 9886 |
rs749680847 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948102 | TGGCTTTTTTTGCCA[C/T]TCTTATCTCCTCTTT | 9886 |
rs749712092 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882115 | AGACCTTTATTTATA[A/G]CACTTTAAAAATAAT | 9886 |
rs749732452 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003404 | TGTGTCTTTATAGTA[A/G]CATGATTTATAATCC | 9886 |
rs749739605 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886782 | GGTTCCAGCAATCCT[A/G]CTGTCTCAGTCTCTG | 9886 |
rs749792648 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908159 | ACTGCCTACCACTGA[C/T]AACTCCTCATCCCAC | 9886 |
rs749808407 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870669 | CAATCCGAACACCAG[C/T]GCACTAATGGTATCT | 9886 |
rs749811459 | snp | A/C | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875010 | CCACGCCACTCGTGG[A/C]GGCTTTGGTCAACTC | 9886 |
rs749821493 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982773 | TGTAAAATGCCTTTC[G/T]CACACATAGTAAGTT | 9886 |
rs749858837 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979972 | TGGCTGGAATATAGT[A/G]GAATGGGAGAGGGAG | 9886 |
rs749934616 | snp | C/T | 1.6793e-05 | 0.00289763 | splice-acceptor-variant | RHOBTB1 | GRCh38.p7 | 10:60892996 | ACCACAACATCAGAC[C/T]TAAAAGGAAATCATA | 9886 |
rs749973014 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974046 | AAAAAATAGTCATCA[C/G]AATTTTCTATCTCCA | 9886 |
rs749977969 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975019 | CTTAAAATGACCTCA[C/T]TGATAACAACCACAT | 9886 |
rs750017251 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904289 | GAGATATAATGGAAA[C/T]ATACCAAATTTGCAT | 9886 |
rs750039332 | snp | C/T | | | utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936284 | TATGGATAGAAGAGT[C/T]CTGCAAAAAACAACA | 9886 |
rs750065701 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934096 | TAAAGAAATTTTACA[A/G]AAAAGAGGGCAAGGA | 9886 |
rs750103394 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895063 | GGGTTGGAAAAAAAG[A/G]AATCTTGTGATGATA | 9886 |
rs750128942 | snp | A/G | 1.74824e-05 | 0.0029565 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910848 | TTTGAAAAGGAAATT[A/G]CATTCAAGCTCAACC | 9886 |
rs750135849 | in-del | -/TAACTC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953976 | GCTTTAAATTTACTT[-/TAACTC]TAACTCTATTCCATG | 9886 |
rs750153655 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943730 | GTTAGGGGTGCGGCT[C/G]TGCGGGCGCTCCTAG | 9886 |
rs750188352 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931938 | ATTCAAAAGGAATAC[-/T]TATGGTAACTGAAAT | 9886 |
rs750221351 | snp | C/T | 8.27301e-05 | 0.00643103 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888490 | GTCATGGGCCCCATC[C/T]GCTTTGAAATGGGGT | 9886 |
rs750257208 | in-del | -/TC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881145 | CCCTTTTCACTTGGT[-/TC]TCTCTCTCTTGCCTG | 9886 |
rs750276676 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980372 | AGGTTATGAATATAC[A/G]ATAAAAAAATGATTA | 9886 |
rs750283804 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888986 | AGGGTGCCTGAAGTA[A/G]AGGTTTCTGGACTTT | 9886 |
rs750284450 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905450 | GAGAGACTCTTTCTC[-/A]AAAAAAAAAAAAAAA | 9886 |
rs750302599 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914741 | TTGTATTAAGGCTAT[A/G]ATTACAAAAACTATC | 9886 |
rs750307202 | snp | A/G | 3.32143e-05 | 0.00407505 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888701 | CGACACTCAATATCC[A/G]CCCCTGGAAATCTCT | 9886 |
rs750329128 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899690 | GAGAACCTACTGTGT[A/G]CCAGGCATTCTTCTA | 9886 |
rs750361723 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926127 | TACTAATCTCAGCTA[C/T]TCGGGAGGCTGAGGC | 9886 |
rs750386004 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954702 | AAAAATTGGATGGAA[A/G]GAAATGTGACAAAAT | 9886 |
rs750408526 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928888 | GAATGGGTAATTTAT[A/G]AAGAAAAGAGGTGTA | 9886 |
rs750419245 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998190 | ATTCATAATTCAGGC[C/T]CACCCTCTCTAACAC | 9886 |
rs750446338 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874420 | AGGCAGAGTTTAGCT[C/T]GTGCTTTGGGGAAGT | 9886 |
rs750451468 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982715 | AGGCTGATACTGTTA[G/T]ACTAATATTACTGAT | 9886 |
rs750475146 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931528 | TCCATTACTTTTTAT[A/G]GCTGAAAAATATTCT | 9886 |
rs750481495 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001937 | AGTTTCTGGCGATGT[C/T]AAGGGTCAGCCTTTT | 9886 |
rs750519412 | snp | C/T | 1.68431e-05 | 0.00290194 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886272 | CATGAGCCAACTTTG[C/T]TGAGAGCTTCAACCA | 9886 |
rs750522637 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901528 | TTTATTGATATGGAA[C/T]AGCTGAAAGATAGGT | 9886 |
rs750535572 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970861 | ACAAAAAATAATCAA[C/T]TGAATGCTAAACAAC | 9886 |
rs750547263 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911520 | TCAACGTTGGGTCTT[C/T]CGTAGTCCATGTCAG | 9886 |
rs750564768 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909202 | AATAAATGCTATGCA[A/G]GAATCTCACAAGATA | 9886 |
rs750577808 | snp | A/G | 1.65597e-05 | 0.00287743 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872148 | TTCCATGAGAGGTGA[A/G]GAGAGCTGGATGAAT | 9886 |
rs750622412 | in-del | -/T | 5.32505e-05 | 0.00515969 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893039 | TTGCCTTTTAACAGG[-/T]TTTTTTCTTTTACCA | 9886 |
rs750631980 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918664 | GGTCTCCTAATTGCT[C/G]TGAATCATCCCGCCA | 9886 |
rs750636215 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884943 | TTTTTTTTAGAGACA[A/G]GTTCTCACTCTGTCT | 9886 |
rs750637631 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966540 | GGAAACTATAATGAA[C/G]AAACCACTACAGTGG | 9886 |
rs750677459 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891902 | ATCGTGGGGGCGGTT[C/T]CCCCATGCTATTCTC | 9886 |
rs750698611 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958516 | GATTTCCAAAACATT[C/T]TTTTTCAGGAGAATC | 9886 |
rs750759973 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963501 | ATATTTAGACAGCAA[C/T]ATTACAACAGAAAGC | 9886 |
rs750775733 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950897 | CTTCCACCAAATTGT[A/G]TGAGGTAGAAAGTTT | 9886 |
rs750852096 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950244 | AATGTATAATGTGTA[C/T]CTTTGACATTTTAAA | 9886 |
rs750860980 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911790 | AAACAGTTTATTCCC[A/G]TTAACTGTTATTTTC | 9886 |
rs750878911 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873963 | TAGGTCGCTGTAAAG[C/T]TCAATTCCGCCTTTT | 9886 |
rs750907525 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900490 | CTCTAGTTCAGCATT[A/G]TTAACCCTGAATTGT | 9886 |
rs750908752 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870431 | AGCAACATGAATTTT[C/T]CCTGGGAAGAGTTAA | 9886 |
rs750958498 | snp | C/T | | | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910893 | TTGGTTTACCTGCCA[C/T]ATGCAAAGCGTCTGT | 9886 |
rs750958891 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940020 | CACAACTAATCATGT[A/T]GATGAGGTCTTGGCC | 9886 |
rs750959407 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994742 | TAGCATAAACTAAAT[A/G]AAAAATAACTGTCAT | 9886 |
rs750986518 | snp | A/G | 0.000115541 | 0.00759982 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888813 | GGAAGAAGAGGTAGC[A/G]AGGTAAATTCGATGT | 9886 |
rs751008878 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982011 | CCTGACCTCAGGTGA[C/T]CCACTGGCCTCGGCC | 9886 |
rs751013426 | snp | A/G | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877935 | CCAAGTGTGGCAGGC[A/G]AAATCTGTTTGCCAA | 9886 |
rs751015477 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951523 | GTTAACTGCATCACA[C/T]GTGGGTGACATAAGC | 9886 |
rs751036406 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994599 | TTTAAAAAGTTAGAT[A/T]TTCTAATGTGAGGGA | 9886 |
rs751055772 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938306 | ACATTGGAAGATTTA[A/G]AAGACTTGGCACTTT | 9886 |
rs751099781 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976210 | TAACAGCATTTCATT[A/G]GGATATTTTATTACA | 9886 |
rs751143270 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916637 | TAGGGATGATGGGTC[A/G]TGCCAACTTTTCTCT | 9886 |
rs751149151 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906375 | TGGAATATCAGAGCT[C/T]GTAATAGATGGTGAG | 9886 |
rs751151414 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923613 | CAATCTCTTGAATAG[A/T]ATGCGATATGGTTTG | 9886 |
rs751170368 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896506 | GCAGAGTACAGGGTA[C/T]ATGAGATTGTAAACT | 9886 |
rs751171719 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899493 | CTCTGGGATTAACCT[-/C]CCCGACTCTTCTGAG | 9886 |
rs751173340 | snp | A/C | 1.68252e-05 | 0.0029004 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888587 | GAACTGCACCCTCGG[A/C]TTCCAGCCCCAGAGC | 9886 |
rs751189433 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911115 | CCTTATTCTATCTGA[C/T]GGGATTTAAGCTAAG | 9886 |
rs751221597 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885395 | CATATGTCTCTTCTA[A/G]AGATAGAGCCAGGGG | 9886 |
rs751271402 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963688 | TGTAAAAGGAGTAAT[A/G]GTTTTTGTGTTATGT | 9886 |
rs751272999 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897228 | CAGTCAAATATAGCA[G/T]AGTTGGTGGGAAAAG | 9886 |
rs751285747 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923865 | ACCATGATTGTGAGG[C/T]CTCCTCAGCCACATG | 9886 |
rs751289668 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927927 | AATATTTGCAAATTA[C/G]CCATCTGACAAGGGA | 9886 |
rs751355357 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968406 | TTAAAACAGGAGTAT[A/G]AGCACCAAAATAACA | 9886 |
rs751358665 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981880 | GTTCAAGTGATTCTC[C/T]TGCTTCAGCCTCCCA | 9886 |
rs751362478 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955835 | TCTTGAAAACTAAGG[A/T]TGTGCTATCACGATT | 9886 |
rs751374472 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927544 | GAAGAGAATAGAGAA[-/C]CCAGAAAAAAATTCC | 9886 |
rs751419551 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905544 | AAGTCAGCATGAGTA[A/G]CAGTGCCATATTGTG | 9886 |
rs751442371 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955756 | CAGAGTTTGAATGCA[A/G]GGGAAACAGGAACCC | 9886 |
rs751446523 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984378 | GGATTTTATTAATAA[A/G]TGTTTTATGCATATG | 9886 |
rs751457036 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878794 | TGCTGGAGTTCGCCA[A/G]AGAGCCAGGCACTGC | 9886 |
rs751492467 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917072 | TCAAGCTCAGTGAGA[C/T]CCATGTCAGACCTTT | 9886 |
rs751503706 | snp | C/T | 1.7321e-05 | 0.00294282 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892801 | GAAACACTGAGTCCC[C/T]TGGCTTACCTTGCTA | 9886 |
rs751535704 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912025 | AATATCTGTTGTTGA[A/T]AAGCAGTTTTCTATA | 9886 |
rs751541846 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966971 | ACGACAAAGTTCTTG[C/G]GGAGAAATATTATAA | 9886 |
rs751570742 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878529 | AGTGACCAGCTTGAT[C/T]TCGAAATTCTGTCAG | 9886 |
rs751585869 | snp | C/G | 3.30808e-05 | 0.00406686 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889147 | TTTGCTACCTCTCGG[C/G]CTTTTTCTGGGGGCA | 9886 |
rs751608188 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989239 | TTTCTTTCTTAAAAC[A/C]CAAATTTGACTGTTT | 9886 |
rs751624760 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931206 | ACGTGCTACACATCT[C/T]ATTCTTTTAAAGTAT | 9886 |
rs751651088 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893368 | GAAAATACAAACTAC[A/C]TTTCACCAGTTTAAA | 9886 |
rs751655300 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979122 | TTTATGCTAGGAACA[-/T]GTATGCTAGGAAAAG | 9886 |
rs751662684 | in-del | -/G | 1.65091e-05 | 0.00287303 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872311 | GAAAAGTGAGCAAAA[-/G]GAGGGTAAGACTATT | 9886 |
rs751683655 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888825 | AGCGAGGTAAATTCG[A/G]TGTGCAAAGATGTGT | 9886 |
rs751705685 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880447 | TCAGATAGGTAGACC[C/T]ATCCCTTAACGTATC | 9886 |
rs751718939 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889262 | GGCCTATCTAAGCAC[C/T]TAATGGAACTATACA | 9886 |
rs751722735 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886320 | GCCACCAAACTGCGA[C/T]TCCCTTACTCTCTCT | 9886 |
rs751738938 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881727 | GTTTTTTGGCAAGAG[C/T]GTGTTCTAAGTCATT | 9886 |
rs751748958 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906932 | TCACATGTCGTGATG[C/T]CGTGGGAGGGACCCA | 9886 |
rs751778729 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921223 | AAAGTGCTGGGATTA[C/T]CAGCATGAGCCACCA | 9886 |
rs751801664 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988058 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 9886 |
rs751805765 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945723 | AGGAAAGTTATCACC[A/G]GCAACCTCATTTGTT | 9886 |
rs751824610 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940128 | TTTTACAGGACAGAC[A/G]TGTTATAGGACAGCT | 9886 |
rs751849156 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924513 | TATTATTAGAGCTAA[-/AG]AGAGAGAGAGAGAGA | 9886 |
rs751851834 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919948 | TATTTCTTGAAAAAA[C/T]AAACCAAAAATTTAA | 9886 |
rs751876236 | snp | A/G | 0.000221641 | 0.0105248 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878097 | AATTCTGCTGCAGAA[A/G]GCAGGGAGTGGGCAC | 9886 |
rs751876265 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951564 | TTCAGGGTCAGCATC[A/G]AAGGTGCACAATCAC | 9886 |
rs751902137 | snp | A/C/G | 3.29518e-05 | 0.00405894 | synonymous-codon, missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872272 | AACACCAGGCGGCCA[A/C/G]CTGGTGGGCATTGTG | 9886 |
rs751927663 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888946 | GGAATTTTGATGACC[A/G]GTGGAGGGGCTTTTG | 9886 |
rs751945044 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995009 | AGCCATGGAGTAACA[C/T]TGTACTCCATGGCTT | 9886 |
rs751977540 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982879 | TGTGCGTTTCATTTG[C/T]CCTCTTTCCTCTTCC | 9886 |
rs751987281 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911921 | CCTGCTAGCAAGTCC[A/G]GTCACCTGTAGGGCT | 9886 |
rs752021075 | snp | A/G | 3.29609e-05 | 0.00405948 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886145 | CACAAATGACCCCCC[A/G]AACATGGCTGCCATC | 9886 |
rs752032594 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902874 | GAGATTTGTCAACTC[A/G]TTCAACTAACATCGA | 9886 |
rs752047466 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983624 | GATTTTGCATTTTAC[A/G]TCTTTGCAAAGAGGA | 9886 |
rs752062815 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891979 | CATCCGCCTTTGCTC[A/G]GTTCTCATTCTTCTC | 9886 |
rs752073417 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901659 | TTCATCAGAAAGTTC[C/T]AGTATAAACACATCA | 9886 |
rs752102511 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930425 | AGAAGTTATGCTTAT[C/G]ATGAGTTTGCAATAA | 9886 |
rs752154328 | snp | C/T | 3.36502e-05 | 0.0041017 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888591 | TGCACCCTCGGCTTC[C/T]AGCCCCAGAGCCTCC | 9886 |
rs752168943 | snp | A/C | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886112 | TAGGAAGGCACGTAC[A/C]TCACTGTTGGCACTT | 9886 |
rs752193495 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923749 | CCATACTGTTCTCGG[A/G]ATAGTGACTAAGTCT | 9886 |
rs752196670 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936169 | TCTGACGTACGTCTT[C/T]GATGTTTCACTTTTG | 9886 |
rs752209179 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885491 | ACATTTGCTCCATTA[C/T]TGTTGCCCTAAAGTT | 9886 |
rs752220466 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963948 | TGAATTTCCAACTGA[A/G]GGGAAAAAACCTTGA | 9886 |
rs752236296 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978142 | TTCAACACCCTCTGC[A/G]TTAAATATATATTTT | 9886 |
rs752262828 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995083 | AAGGTGTGACTAAAG[A/G]TCATAAATAGCTCCC | 9886 |
rs752310212 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898186 | ATTGTGGTCACATTT[G/T]AATGGGCTTCTTTTC | 9886 |
rs752350551 | snp | A/G | 3.31186e-05 | 0.00406918 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875067 | AGAGAGGGGGCAGGA[A/G]AACATTAAACCACGC | 9886 |
rs752352544 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871010 | TAACCCTCTAATTAC[A/G]TAATAATGCTCGGTG | 9886 |
rs752356271 | snp | C/T | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875000 | CCGTCAATGCCCACG[C/T]CACTCGTGGCGGCTT | 9886 |
rs752367465 | snp | C/T | 1.67632e-05 | 0.00289505 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877901 | GGCCCTGAGTCATCA[C/T]CCTTACCTGCAAGTG | 9886 |
rs752398511 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952468 | TCATTAACTCCTCAC[A/G]ATGACTTAATGAAGG | 9886 |
rs752400193 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886371 | TTTTATGTCAATCCC[A/C]ATCTTTGAGCTTTGA | 9886 |
rs752424942 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917349 | TGTCACAAAAGCTTT[C/T]CTAACTATCCTCTAA | 9886 |
rs752426556 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912082 | AGAATAATCAAAAGT[G/T]CAGGCTGAAAGACTA | 9886 |
rs752430118 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880086 | CAAATACGATGCCAT[C/T]TTATATGAGGAATTT | 9886 |
rs752480138 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970744 | TGCTTACTTCACATT[C/T]ATATTTTTGTCACAA | 9886 |
rs752483769 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958894 | GTGTGAGGCACCGCA[C/G]CTGGCCCAGAGTAGG | 9886 |
rs752488642 | in-del | -/TAAAAAAATGCTGTTGGGAAAAC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971458 | GAAAGGATTCCCTAT[-/TAAAAAAATGCTGTTGGGAAAAC]TGGCTAGCCATATGC | 9886 |
rs752494917 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946394 | AAACTCAAAAGAAAT[A/G]GGAATCAACATGTAT | 9886 |
rs752545105 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957417 | TTTCAGCTCCATTAT[A/G]ATGTTATGGGACCGC | 9886 |
rs752546586 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897425 | GACTTTCCTTTTCTA[A/G]TATCATTTATTTTGC | 9886 |
rs752576931 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937019 | AATTGCACCACCAGG[A/G]TAATATAGTCTATTC | 9886 |
rs752585596 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996104 | AAGAACTCATAGCTC[A/G]TAAATGGAGGAGCTC | 9886 |
rs752586229 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878950 | CTTGGATTTTTGGAA[A/C]ATTGACAATTATAAA | 9886 |
rs752587160 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891746 | TGTTTTTTTATAAAG[A/G]GGATTTGAGGGAACT | 9886 |
rs752604681 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906736 | TCACTGTCAGCAACA[C/T]AGGCTTTATTCAGTG | 9886 |
rs752610375 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988650 | TTTGTTACTTTTATG[G/T]CTACAAAGTATTCCA | 9886 |
rs752611981 | in-del | -/CGGTACTGGTCAATCGCCCACA | 1.6684e-05 | 0.00288821 | frameshift-variant, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911363 | ACCTCCTGGCACACG[-/CGGTACTGGTCAATCGCCCACA]CGGTACTGGTCAATC | 9886 |
rs752616004 | snp | A/G | 9.89348e-05 | 0.00703261 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892950 | TTTCACATGATTTAG[A/G]GAATTGGGATTAGCA | 9886 |
rs752644143 | snp | C/T | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888263 | GATTGGCTTTCCTTA[C/T]GTGAAAGGCTTTCGT | 9886 |
rs752675052 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935103 | CATCAACAGTAAAAT[C/G]GATTAAAAATAATAA | 9886 |
rs752731998 | snp | A/G | 3.60575e-05 | 0.00424587 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888163 | TCTGGCTAACGTTCA[A/G]TGAAACACAATCAAA | 9886 |
rs752739792 | snp | G/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003343 | ATTGATGGACATTTG[G/T]GTTGGTTGCTATTGT | 9886 |
rs752758876 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907530 | AAAAAGGCCATAAGA[A/G]AGCTGGAGTTATTCA | 9886 |
rs752772350 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888850 | ATGTGTTCCTGGTCC[C/T]GAAGGATGAACAGAA | 9886 |
rs752825478 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883116 | GGAAGGGGCGAGAAT[A/G]TCGACAGCTCATTGC | 9886 |
rs752880669 | snp | C/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886129 | CACTGTTGGCACTTT[C/G]CACAAATGACCCCCC | 9886 |
rs752898533 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980707 | AAGAAAAAGGAAAAA[C/T]CTAAACATTGATGAA | 9886 |
rs752935754 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899722 | ACATTGGGGATAGAG[G/T]GATTAGTAAAAGACA | 9886 |
rs752947298 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930504 | TGAAATACATTCGAC[G/T]GAAACAACAGTAAAT | 9886 |
rs752956626 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937493 | TTATCTGGCTGGAAA[C/T]AGTGGCTTTGAGATA | 9886 |
rs752968691 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888968 | GGGCTTTTGGAGGTA[A/G]GAAGGGTGCCTGAAG | 9886 |
rs752980682 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984848 | TACACATTTTAGACA[C/T]AGAATAAACAATTTT | 9886 |
rs752993074 | in-del | -/GTTCATGA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933853 | TTGTTATATTGAGAT[-/GTTCATGA]ACAATCTTTAAATTA | 9886 |
rs753076884 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886185 | CTACAGATCAGCAGC[A/G]GCTTGTGGGCACTGA | 9886 |
rs753087995 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983837 | GAGCTTCCCGGCCCC[A/G]CCCTCCTTCTGGCCT | 9886 |
rs753139050 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984991 | ATGATTTGTTGAAGT[A/T]ACTATATGTAGTTAA | 9886 |
rs753141152 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972623 | AAACCACCATGGCAC[A/G]TGTATGCCTATGTAA | 9886 |
rs753173858 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967538 | GGATGGCAATCCTGA[C/T]GGATGAGAAAAAGAA | 9886 |
rs753211352 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881833 | CAGTGAGCAGCCCTG[C/G]CCAAACACCCTCAAT | 9886 |
rs753212767 | snp | C/T | 8.33146e-05 | 0.00645371 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911364 | ACCTCCTGGCACACG[C/T]GGTACTGGTCAATCG | 9886 |
rs753264874 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903955 | CTTTGTCCATAAGGA[C/T]ATTTCTTTTCTTTTC | 9886 |
rs753287018 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931349 | CTTTATTCTCGTTCT[C/T]CCCAGCTCTGGCAAC | 9886 |
rs753288793 | snp | A/G | 1.65721e-05 | 0.0028785 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877924 | TGCAAGTGCAACCAA[A/G]TGTGGCAGGCAAAAT | 9886 |
rs753304501 | snp | C/G/T | 5.03219e-05 | 0.00501586 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911018 | GAGAGAGCATCTGTG[C/G/T]TCGGTGTCAGTCAGA | 9886 |
rs753307317 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959699 | TTCCAGTTATGTGTA[C/T]TTTGGAAAGACACTT | 9886 |
rs753315710 | snp | A/G | 8.24953e-05 | 0.0064219 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871489 | CTTCCTCTTCAGGCC[A/G]CTGCTGGAGATGAAT | 9886 |
rs753328387 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925997 | GCACTTTGTGGGGCC[A/G]AGGCGGGCAGATCAC | 9886 |
rs753333927 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920538 | TCAGCCTTTCAGGCC[A/T]TAGTCAGGAGTTTGG | 9886 |
rs753336609 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913514 | TGGTTTTCTTAGTTA[C/T]CCATCTAACAGTATA | 9886 |
rs753338597 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898861 | AAGTGGGGCCAAAGC[A/C]ATGCATGCTCTTAAG | 9886 |
rs753356755 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996842 | AGGCATCCTGTATTT[C/G]ATTTGCAAACTTATC | 9886 |
rs753362376 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985079 | TCAGATATGCCCACC[A/G]TCTTAATTCTTTGGA | 9886 |
rs753399429 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966130 | ATTTGAAAGGAATAA[C/T]GTCTTGAAAAGATTG | 9886 |
rs753432903 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900026 | AACAGAGCAAAGGCC[C/T]GAGGTAGGAGCCTGC | 9886 |
rs753436126 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887240 | TCAAGACTGTTTCTG[C/T]AACACAATGGCCAGT | 9886 |
rs753484423 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944884 | GGACGCACCGCTGAC[C/T]CCGACCCGGGTACAG | 9886 |
rs753487210 | snp | G/T | 4.94972e-05 | 0.00497455 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892957 | TGATTTAGGGAATTG[G/T]GATTAGCAATCGAAA | 9886 |
rs753537522 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943003 | GAACAGCACAGGATG[C/G]GGAAGTTCAAAGTCA | 9886 |
rs753571584 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914239 | TAATGAGAAGATAAT[A/G]GAGTTGGAAAGATGG | 9886 |
rs753573362 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870193 | AAGCAATGACTGACT[A/G]CCTCACGAAAGCTCC | 9886 |
rs753617126 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935277 | AGTCCAAAAGCAGGC[A/G]AAACTAATTTATGGT | 9886 |
rs753629235 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938909 | TTTGGCATCTAGTAG[A/G]GGCATAAATGCTAGT | 9886 |
rs753632208 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959291 | CTTGCTCTTGGAAAA[C/T]GGACCTACAGTATGG | 9886 |
rs753667397 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947706 | TGCATGGATGTATCA[C/G]AGTTTGTTTATCCAT | 9886 |
rs753711782 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989735 | AAACTGAGGCTGTAG[A/C]TCAGGGAAGTCCCCA | 9886 |
rs753711838 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978335 | ATCTCCAACCCCATA[A/T]TTAAAGTCTTCTCCC | 9886 |
rs753750346 | in-del | -/GA | 0.000819898 | 0.0202306 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910997 | CTCCAAGACCTGCAG[-/GA]GAGAGAGAGAGCATC | 9886 |
rs753764783 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979112 | GGCTCTAATATTTAT[A/G]CTAGGAACATGTATG | 9886 |
rs753780988 | snp | A/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888380 | GAGCCAGGCCCACCA[A/T]ATCCTTTTCCTTTTC | 9886 |
rs753810051 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938511 | GGCTCCATGATTCAA[C/T]TCTCTATGACTCAAC | 9886 |
rs753810456 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925024 | CATCCTCTTGGTGAT[A/C]AGTGAACTCTTGCTC | 9886 |
rs753820695 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919123 | CCATGGAGGGACCTT[G/T]GTAGTCTTATCTCCA | 9886 |
rs753831757 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999697 | ATGCCAAGAGGCATA[G/T]TTCATGGATTAGACT | 9886 |
rs753888660 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980884 | ATGCCCATTCAAAGA[A/G]CCACTTCCCTCTCTG | 9886 |
rs753935242 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912185 | AAATTCATAATTCAT[-/AA]ATATATATGTGTGTG | 9886 |
rs753944672 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889100 | CAAACTGGTCAAACA[C/T]GCTTGTTTCATAGTA | 9886 |
rs753948145 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981832 | TGGGGTGCAATGGTG[C/T]GACCTCGGCTCACTG | 9886 |
rs753963530 | snp | A/T | 1.671e-05 | 0.00289045 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886258 | TGAGGAAACACAACC[A/T]TGAGCCAACTTTGCT | 9886 |
rs753968705 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872687 | GGAATACTTCGTGTC[A/G]CATGTCAGAGCTCAG | 9886 |
rs753978824 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987767 | CCAAGATCTGAGATC[A/G]ATATGTTTTACCACT | 9886 |
rs754018377 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871522 | CAGAAGCACCACTTT[C/T]GTCTTGAGCGATGCT | 9886 |
rs754030927 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969926 | ACACCTGAGAGAAGA[A/C]TATAGGACTTCAAAC | 9886 |
rs754045911 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928095 | TCATTCGTCATCAGA[G/T]AAATGCAAGTGAAAA | 9886 |
rs754047191 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916612 | TTTTGAATGGATGAT[C/T]TTTTCCACCTAGGGA | 9886 |
rs754076115 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928726 | AGCACAATGGGGCAA[A/C]TATAGTAAATTAACA | 9886 |
rs754129348 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939704 | CAGAGGGAAACGTGA[A/G]TGGCCTATTTTCTAA | 9886 |
rs754137226 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886195 | GCAGCGGCTTGTGGG[C/T]ACTGATGGCTCCATC | 9886 |
rs754151635 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881915 | TTTGCTGAATATAAC[A/G]TTAACATTTTTTGAA | 9886 |
rs754192542 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995474 | GCTGCTTTGCAAATT[A/C]TCTCTGATAACCTCA | 9886 |
rs754214593 | snp | C/T | 1.6552e-05 | 0.00287676 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60871606 | TCTTCTTCCTTCAGG[C/T]ACCACACAGGGGGCC | 9886 |
rs754215497 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894760 | AGAATTGAGGAAATA[C/T]ATCCAGCACCTAAAT | 9886 |
rs754238544 | snp | A/G | 1.65619e-05 | 0.00287762 | stop-gained, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911371 | GGCACACGCGGTACT[A/G]GTCAATCGCCCACAC | 9886 |
rs754333457 | snp | A/C | 1.65798e-05 | 0.00287917 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875078 | AGGAGAACATTAAAC[A/C]ACGCCCTGCGAGCCA | 9886 |
rs754351992 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909661 | AAAAAAGCAAAATGG[C/T]ACCTAAGATAACAAT | 9886 |
rs754403107 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921093 | AGCTGGGATTACTGG[C/T]ACCCACCATCATGCC | 9886 |
rs754408801 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991712 | CTGGGATTACAGACA[A/T]GAGCCACCGCACCCG | 9886 |
rs754436132 | in-del | -/A | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876021 | GCATGCTTATTGGTC[-/A]GTATGCCTATATCTG | 9886 |
rs754449195 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911491 | TGTCACCCACGACCA[C/T]ACATTTGATAGTTTC | 9886 |
rs754449291 | snp | A/C | 1.68437e-05 | 0.00290199 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888608 | GCCCCAGAGCCTCCA[A/C]CAGGCTCTTGTTTGA | 9886 |
rs754450840 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906376 | GGAATATCAGAGCTC[A/G]TAATAGATGGTGAGT | 9886 |
rs754451034 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962211 | ATGTCTATGCATTAT[A/G]AAGTTTATATGCAGC | 9886 |
rs754469131 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934252 | TCATATGGTAGGGAA[C/G]AGGCTTGCTGCTCCT | 9886 |
rs754480067 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995928 | AGGAGCATATCATAG[C/T]ATTTATGCACCATTA | 9886 |
rs754480832 | snp | A/G | 1.65726e-05 | 0.00287855 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888507 | CTTTGAAATGGGGTT[A/G]ACTTGCATTTCCCTG | 9886 |
rs754482209 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963773 | GTATCAAGTAATTTA[A/G]TATCACTTTCCAAAT | 9886 |
rs754493936 | snp | A/C | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884818 | GTAGAAGAGTGATTA[A/C]CAGAGGCTGGGATTA | 9886 |
rs754513012 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894618 | TCTATTATTCATAAT[C/G]ATATTTATATCAGGT | 9886 |
rs754531956 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962671 | GTATTTAAAGCTTCT[A/G]TCCTTCGGTAAAGTC | 9886 |
rs754543214 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896508 | AGAGTACAGGGTACA[C/T]GAGATTGTAAACTCC | 9886 |
rs754600998 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951599 | CTTGTAAACATAAGC[C/T]GATGATTCCAGGGAT | 9886 |
rs754663473 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985558 | AAAGAATTTTAACTG[C/T]GTATAAAGTGGATAG | 9886 |
rs754682805 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949039 | GGCTGTTGGGCTCCA[-/G]CTAGTGATGACAAAC | 9886 |
rs754733541 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999380 | AACAACAAAAAAGAT[C/T]CCTTGTATCAGTATT | 9886 |
rs754736535 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916311 | GCTGAGGCAGCCCTG[A/C]CAATGGCTGTCACCA | 9886 |
rs754742920 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914887 | AAGTGACTGCCAAAG[A/G]TGCTGACCCTTGTGC | 9886 |
rs754778342 | snp | A/C/T | 3.31511e-05 | 0.0040712 | missense, stop-gained, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889154 | CCTCTCGGCCTTTTT[A/C/T]TGGGGGCAAAATATC | 9886 |
rs754784805 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984547 | ATTAACTGAAAACCC[A/G]TAAGACAGAACTTCT | 9886 |
rs754789440 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928065 | TAGCCAACACATATG[A/C]AAAAATGCTCAACAT | 9886 |
rs754850584 | in-del | -/TGAC | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870184 | TTTACAGAGAAGCAA[-/TGAC]TGACTGCCTCACGAA | 9886 |
rs754862010 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955845 | TAAGGATGTGCTATC[A/C]CGATTGATGAAGTAT | 9886 |
rs754868506 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876889 | AAAGTCAAGTGCAGA[C/T]AGGACTGGTTGGTTT | 9886 |
rs754910610 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987622 | TGTTCCTGCTTCCAA[C/T]CTCCCATCATTTCCC | 9886 |
rs754947760 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975245 | AGGGGAATTCGTCAG[A/C]ATGTGTAAATGGCTG | 9886 |
rs754955960 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994605 | AGTTAGATTTTCTAA[-/C]TGTGAGGGAAAGATA | 9886 |
rs754963825 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878836 | AGAGCTGTAGAGGTG[A/G]GCATGGATTAATGGA | 9886 |
rs754971314 | snp | C/T | 1.72225e-05 | 0.00293444 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892805 | CACTGAGTCCCTTGG[C/T]TTACCTTGCTAACGG | 9886 |
rs755002518 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905571 | TGTGTCTGAGGCAGA[A/C]GGGAAAAAAAAACCA | 9886 |
rs755011040 | snp | A/T | 1.65875e-05 | 0.00287984 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888719 | CCTGGAAATCTCTGC[A/T]CTGCTTCTCTTTCTC | 9886 |
rs755012822 | in-del | -/A | 1.68203e-05 | 0.00289998 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878072 | CCTGAAATGTTATAC[-/A]AAAAAGCTAAATTCT | 9886 |
rs755031231 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881744 | TGTTCTAAGTCATTG[C/T]TTAAAGAAGAAATAG | 9886 |
rs755038740 | snp | C/T | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869041 | TATTTTCACAAAGGC[C/T]TTCTCAGACCTGCTT | 9886 |
rs755088595 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000669 | GAATGTATATCTTCA[-/T]TTTTTTTTTAATTCC | 9886 |
rs755092817 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947788 | ATGAAAAACACTTCC[A/G]TAAACATTTGTGTAT | 9886 |
rs755111291 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921308 | TATGTACAGAGAACA[C/T]GTCATGAGGGCAGGG | 9886 |
rs755129600 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936613 | GATATAGTAACCACT[A/G]TTCTTTAGAACCTCA | 9886 |
rs755199174 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900589 | TTAATTTCTCTCTCA[A/T]TGTGCGCACACAGTG | 9886 |
rs755207476 | snp | A/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888832 | TAAATTCGATGTGCA[A/G]AGATGTGTTCCTGGT | 9886 |
rs755263137 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931756 | TTTCTTTCTCTGACT[C/G]AAGCTCTCACATAAA | 9886 |
rs755269611 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870329 | TCCGTGTAGGAGAAC[A/G]CAGGCGCCCAGCCTC | 9886 |
rs755275538 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941020 | ATGCCAGAAAGTACA[A/C]ATGAATACTTACAAT | 9886 |
rs755278154 | in-del | -/AT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951908 | CTAAAAATACAAAAA[-/AT]TAGCCGGGCATGCTG | 9886 |
rs755332757 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952340 | CTAGTGCACATGATA[A/G]TAATAAACACCAAGA | 9886 |
rs755335127 | snp | A/C | 1.65146e-05 | 0.0028735 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874978 | TTCCAAGTAAGAGAG[A/C]ACTTCTCCGTCAATG | 9886 |
rs755340102 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900809 | TCTTCAGACTGTTAA[C/T]GCTGAAAGACTGCCA | 9886 |
rs755374203 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929324 | AAAATGAAAAATTAA[A/G]AAAACAGATTCTTGA | 9886 |
rs755390013 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958655 | GTTGCCCATGCTGGA[A/G]TACAGAGGCATGATC | 9886 |
rs755405180 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940153 | ACAGCTTATAATATC[A/C]CTTTAAATGCTTAAA | 9886 |
rs755422672 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880457 | AGACCCATCCCTTAA[C/T]GTATCATAGGGAAGG | 9886 |
rs755436774 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971133 | ATTTAAGTAAATTAT[C/T]CATCTGATACATGAG | 9886 |
rs755439315 | in-del | -/GTTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920639 | TTTTTTTTTTTTTAA[-/GTTTT]GTTTTGTTTTGTTTT | 9886 |
rs755439869 | snp | A/G | 1.66743e-05 | 0.00288736 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886062 | TATATAAATACACAG[A/G]CACACATACATTCAT | 9886 |
rs755446843 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002043 | ACACATGGCTTAGTC[A/G]TTTACTAATGGTCCT | 9886 |
rs755475506 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891983 | CGCCTTTGCTCGGTT[C/G]TCATTCTTCTCTCTC | 9886 |
rs755505364 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003013 | TATACATGTGCCATG[C/T]TGGGTTGCTGCACCC | 9886 |
rs755506873 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980440 | GATTAAAAATGTCCC[-/T]CCTTAACATTGTCTG | 9886 |
rs755508880 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995146 | TTATGAGTATATCAA[A/T]GAAAATAATATACCA | 9886 |
rs755549950 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912131 | TAAACTGCTAAGTCT[A/G]AATTTAATCAAATTA | 9886 |
rs755555855 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896788 | AAATAATGTCCATGA[A/G]ATAATGTTTTGACTA | 9886 |
rs755557344 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972502 | AGAACACAGGGACAC[A/G]GGAAGGGGAACATCA | 9886 |
rs755610611 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930481 | GGGGAAAGTGTGGAA[C/T]AGTAATGTGAAATAC | 9886 |
rs755616830 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874210 | ATTTATTCTTAGTTT[C/T]CTCAGAGTGTAAATT | 9886 |
rs755620044 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975655 | ATGAATACCTGATTA[C/T]ACATAAATTCTCTTT | 9886 |
rs755632540 | snp | C/T | 1.65663e-05 | 0.002878 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875070 | GAGGGGGCAGGAGAA[C/T]ATTAAACCACGCCCT | 9886 |
rs755647302 | snp | C/T | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875007 | TGCCCACGCCACTCG[C/T]GGCGGCTTTGGTCAA | 9886 |
rs755664919 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951696 | CACGGAAGCTTCATG[C/T]TTCTCCATCCCCATG | 9886 |
rs755720383 | snp | A/C | 1.68298e-05 | 0.00290079 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888594 | ACCCTCGGCTTCCAG[A/C]CCCAGAGCCTCCACC | 9886 |
rs755796129 | snp | C/T | 1.66421e-05 | 0.00288458 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889161 | GCCTTTTTCTGGGGG[C/T]AAAATATCCCCTCTC | 9886 |
rs755808166 | in-del | -/TAC | | | cds-indel, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871117 | TTCATTTCAACAAAA[-/TAC]AACAGACCATATAAA | 9886 |
rs755810608 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928830 | TTGAGGTTATGGAAA[C/T]CCCAATGTAGTAGTC | 9886 |
rs755815399 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982943 | AGGGAAAGGCGGTGC[A/G]CATGACATAAGGCAC | 9886 |
rs755852909 | snp | C/T | 1.65842e-05 | 0.00287955 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875080 | GAGAACATTAAACCA[C/T]GCCCTGCGAGCCAGG | 9886 |
rs755916913 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905646 | CATTTTATGCCCAAA[A/G]CGAGTGACTCCCTCA | 9886 |
rs755918855 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917357 | AAGCTTTCCTAACTA[A/T]CCTCTAAAAAGCTTT | 9886 |
rs755927978 | snp | A/C | 1.68055e-05 | 0.0028987 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892822 | TACCTTGCTAACGGG[A/C]GCCTGGCTCGATTAA | 9886 |
rs755932991 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961827 | TTTTTTTTTTTTTTT[-/G]AGACAGAGTTTCCCT | 9886 |
rs755942993 | in-del | -/TTCAATCA | 1.65782e-05 | 0.00287904 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874930 | GAACACACTTAAAAG[-/TTCAATCA]GTAAAAAGCAAACTG | 9886 |
rs755944662 | snp | G/T | 1.80383e-05 | 0.00300314 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888164 | CTGGCTAACGTTCAA[G/T]GAAACACAATCAAAG | 9886 |
rs756001752 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898215 | TCTTTGTCACTGTGC[A/G]TGAGTCCCCCTCTGG | 9886 |
rs756048990 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935130 | ATAAATTGAGGACTA[C/T]TTATACAATGGAATA | 9886 |
rs756049087 | snp | A/C/G | 3.30269e-05 | 0.00406356 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872160 | TGAGGAGAGCTGGAT[A/C/G]AATGGGGGCCTCACA | 9886 |
rs756053391 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938808 | AGCTCTGTTTCCTAG[C/T]AGTTCTTTAAAATCT | 9886 |
rs756076607 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885501 | CATTACTGTTGCCCT[A/G]AAGTTAACAAACCCT | 9886 |
rs756144123 | snp | A/G | 8.26139e-05 | 0.00642652 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888264 | ATTGGCTTTCCTTAC[A/G]TGAAAGGCTTTCGTA | 9886 |
rs756153141 | in-del | -/TTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891334 | GTTGTTGCTGTTTGC[-/TTT]TTTTTTTTTTTTTTT | 9886 |
rs756158143 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888982 | AGGAAGGGTGCCTGA[A/G]GTAAAGGTTTCTGGA | 9886 |
rs756159814 | snp | C/T | 3.33272e-05 | 0.00408197 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886071 | ACACAGGCACACATA[C/T]ATTCATAAAGACACC | 9886 |
rs756160942 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979807 | AGGTAGTTAGTGAAG[G/T]TCTTATTGAGAAGGT | 9886 |
rs756187525 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924273 | ACACTATTTGAAGAC[A/G]ATTTTAAAAACATGT | 9886 |
rs756219057 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936822 | TTGGTAAAAATAAAA[A/G]CTTACATATAATCAA | 9886 |
rs756223703 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909359 | GGTATTGACAAATGC[A/C]TAAATTTCTAGTGGC | 9886 |
rs756241558 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903016 | GGAGCCAATTTTCCC[A/G]CAATACAGTTATTGC | 9886 |
rs756245417 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985062 | TCAGCTTTCCCACAA[A/C]TTCAGATATGCCCAC | 9886 |
rs756252711 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950045 | GCAAATTCTGCAACT[C/G]TAACTGCAGTCTTTC | 9886 |
rs756288413 | snp | A/G | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888952 | TTGATGACCGGTGGA[A/G]GGGCTTTTGGAGGTA | 9886 |
rs756337483 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968452 | GATTCTTAAAAATAG[C/T]AGGATATCTCTTATG | 9886 |
rs756356001 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886131 | CTGTTGGCACTTTCC[A/G]CAAATGACCCCCCGA | 9886 |
rs756359768 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938210 | ACCATATCTTTGCAC[C/G]ACTGGAATTCTCTTA | 9886 |
rs756396827 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926490 | TCCTCAATATAATGC[A/T]AGCAAATCAAATTCA | 9886 |
rs756412661 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931470 | TTCTTTCACTTAGCA[C/T]AGTATTTTCAATTTT | 9886 |
rs756421802 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893587 | TTTGCAGGAATTTTG[A/C]CTCTTTACTAAGTAA | 9886 |
rs756435137 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993963 | CTGAGGTTCTTAGCC[C/T]GAGATCCATGAACTT | 9886 |
rs756459683 | in-del | -/TA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996308 | CTGCCCAAGCTGATT[-/TA]TATCAGTATTCTGAA | 9886 |
rs756469750 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918936 | TTTTTAGTAGAGATG[C/G]GGTTTCTCCATGTTG | 9886 |
rs756475933 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886446 | TCACACATAAAGTCA[C/T]GGCACAAACTCTCTG | 9886 |
rs756479020 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892310 | TATAGGTCCGAATGA[C/T]TTTCAAAAAGTGGAC | 9886 |
rs756501112 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942933 | GGGGGTGGGGGAGCC[C/T]CAAACCAGTGAAATC | 9886 |
rs756524843 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930547 | CCCAAATAAAATTGG[A/G]CCTCATGCATTCACA | 9886 |
rs756525233 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949125 | AAAGAAAATGACTTG[A/T]CCTCCTGGGACCTCT | 9886 |
rs756540400 | snp | A/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003380 | TGCCGCAATAAACAT[A/T]CATGTGCATGTGTCT | 9886 |
rs756548945 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973568 | AGCTTGCTGAGTTTC[A/T]TATTCAAAAGAAACA | 9886 |
rs756572569 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870435 | ACATGAATTTTCCCT[A/G]GGAAGAGTTAAAAAT | 9886 |
rs756594632 | snp | A/G | 1.66676e-05 | 0.00288679 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888536 | TGTGCATGCCAATGA[A/G]CCCCTTACTCCATCC | 9886 |
rs756597063 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921816 | TTGGTGAGAGAAACA[A/C]CTTGAGGGACATCTG | 9886 |
rs756647351 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920239 | GAAAAGCAAGCCAGC[A/G]GTGGTTCACAGTCAG | 9886 |
rs756652578 | in-del | -/A | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002698 | AAACGAGCTGATAGT[-/A]TAGGAGATCCAACAA | 9886 |
rs756665909 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876434 | GAGAAATCAATCCCA[A/T]GTTTTCATTGCCAGA | 9886 |
rs756684349 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903035 | TACAGTTATTGCTAC[A/G]ATAGGGATTTGCAAA | 9886 |
rs756691307 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998149 | GAGGGCGGCCCTGTC[A/G]TCTCCATTATGGTAC | 9886 |
rs756753952 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954433 | CACTGAATGAATTCT[C/T]TCCATGTTCTTTTTA | 9886 |
rs756783988 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914505 | GATAAATGTCATATA[A/G]AGCCAATCCCTAAAA | 9886 |
rs756799280 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941932 | CTAAAATTTTCAACA[A/T]ACGTTGTTTTCTCTT | 9886 |
rs756845072 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913533 | TCTAACAGTATAACA[C/T]AGCAAAAGCATGAAT | 9886 |
rs756857437 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934685 | GCCTTAATGATCAGC[-/T]GCCAAATTTAGCCTT | 9886 |
rs756892181 | snp | A/G | 1.65666e-05 | 0.00287802 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877926 | CAAGTGCAACCAAGT[A/G]TGGCAGGCAAAATCT | 9886 |
rs756903582 | snp | A/G | 1.6549e-05 | 0.0028765 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892969 | TTGGGATTAGCAATC[A/G]AAAAACAGAGGACCA | 9886 |
rs756950802 | snp | C/T | 1.76808e-05 | 0.00297323 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888195 | GTATTAATGGCTCTG[C/T]CCCGCGGCCCACTCA | 9886 |
rs756982756 | snp | A/T | 0.000148308 | 0.00861 | synonymous-codon, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872189 | CACAGTCTCACCTGC[A/T]GATTTTGATTTGATT | 9886 |
rs756995586 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898268 | TGACCTTCTTTGGGG[C/T]TTCAAGCTTCTTTTT | 9886 |
rs757023220 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991204 | GTAGCCAGAAATATA[-/T]TTTCAAAATGTAAAA | 9886 |
rs757042919 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888383 | CCAGGCCCACCAAAT[C/T]CTTTTCCTTTTCATC | 9886 |
rs757052446 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936437 | GCGTATGCACATACA[C/T]GCATTTTACTTTTTT | 9886 |
rs757057732 | in-del | -/TG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974907 | ATGTATGGGGATGAC[-/TG]TATTTTTTATAAGCA | 9886 |
rs757065317 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978348 | TATTTAAAGTCTTCT[A/C]CCAAAGGGCTTTATG | 9886 |
rs757070619 | snp | A/G | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888277 | ACGTGAAAGGCTTTC[A/G]TAATCTCCTGGTTCA | 9886 |
rs757073250 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948826 | TGGCTTCCTAAAGAG[A/G]AAGAGGCTGGTGACA | 9886 |
rs757082133 | in-del | -/AATT | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002210 | AATTTTTAAATAAAC[-/AATT]AATATTAGAAACCCG | 9886 |
rs757131375 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919155 | TTAGCTGTTCACAGA[C/G]AGTCTGAATGATGCT | 9886 |
rs757171471 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887516 | AACCCATATTGGATG[C/T]GGGCCACCAGCATGC | 9886 |
rs757180048 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870277 | AGAACGAACTCACAA[C/T]AGCACCATTTCCTAG | 9886 |
rs757212525 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999783 | TTTATGGTTCAGACA[C/T]ACATGAACCAGGGCT | 9886 |
rs757214347 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996880 | TTTTGTGGATATTAA[G/T]CTTATCTCTCAGCTG | 9886 |
rs757237815 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872290 | GGTGGGCATTGTGAA[A/G]CTGCAGAAAAGTGAG | 9886 |
rs757248573 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886201 | GCTTGTGGGCACTGA[C/T]GGCTCCATCGTCCAA | 9886 |
rs757275414 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968660 | TCTCAAAACCTACAT[A/G]TAAGTAAGCCTCAAA | 9886 |
rs757313762 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959483 | AGTCCATTAAAAATG[C/T]GATTGCTCTACACAT | 9886 |
rs757363753 | in-del | -/CACCAGCCAGTCTCGAGGAATCA | 1.65459e-05 | 0.00287622 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872322 | AAAGGAGGGTAAGAC[-/CACCAGCCAGTCTCGAGGAATCA]TATTTTCTAAAGAGG | 9886 |
rs757365479 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900430 | ATAATGATAAGCTTT[C/T]TCGTGAGCTATTTAT | 9886 |
rs757389045 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938598 | GCCAATTTATCCAGG[A/C]AAAAATGTTGTGTAG | 9886 |
rs757427907 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879275 | AGAACAATAAAGCAT[A/C]ATATTTTATTAATGG | 9886 |
rs757437383 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882037 | TTTCCCCTCATGGCT[A/G]ATTTTTTAAAAAAGC | 9886 |
rs757441366 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938925 | GGCATAAATGCTAGT[C/T]TATTGTTATCACAGC | 9886 |
rs757459912 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962921 | TTTCAATGTATGCCA[-/T]TTCCTAATCTAGAGT | 9886 |
rs757491814 | snp | A/G | 1.64817e-05 | 0.00287064 | stop-gained, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871523 | AGAAGCACCACTTTC[A/G]TCTTGAGCGATGCTT | 9886 |
rs757501901 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964616 | CATTTCTTGTTCTAT[C/T]AGAAAACAGCTGCTT | 9886 |
rs757534121 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921102 | TACTGGCACCCACCA[A/T]CATGCCTGGCTAATT | 9886 |
rs757543461 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916636 | CTAGGGATGATGGGT[C/G]ATGCCAACTTTTCTC | 9886 |
rs757548496 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972919 | ATGTTAACAAAACTC[C/T]CCTTTTAAATAGAAA | 9886 |
rs757559454 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883353 | GCATTCACATTCGCT[A/G]CCAAGTTTTTGTTTT | 9886 |
rs757584484 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986966 | GAAATTGTTGATTGC[C/T]GGTGGCTCCAGGCCA | 9886 |
rs757594805 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890492 | GAGGACAAATCTTTG[G/T]AAACAGTAGATGCAG | 9886 |
rs757665357 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920301 | TACATCATCACAAAT[G/T]TGGGGGGTCCTTGAA | 9886 |
rs757688835 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950132 | GAGGAGGTAGCAAAC[A/T]GTTTTTATGGTCATC | 9886 |
rs757690933 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946170 | GCGACAGAGCAAGAC[C/T]CCTTCTCAGAAAAAA | 9886 |
rs757691243 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991945 | TCTTCCCCTTCTAGT[C/T]CATAGGCTAAATGGA | 9886 |
rs757733151 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872823 | GATCCAGATACTCCA[C/T]CCTTCCATTCTAAGC | 9886 |
rs757734428 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884416 | TACTTTTTTAAAAAA[A/G]ATGTTAAAAATACTT | 9886 |
rs757742001 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961266 | GAAGAACATACTATG[A/G]GATGACACAGTATGC | 9886 |
rs757776740 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950853 | TTCCTCCCTCCCCAA[A/G]TGCTGACTGTAAGTA | 9886 |
rs757778830 | in-del | -/ATA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924423 | ACAAAGAAGGTCATT[-/ATA]TAATGACAAAGGGGT | 9886 |
rs757784263 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871882 | ACCACCTGATTTCAG[A/C]GTCTAAGCCTGCTCC | 9886 |
rs757789779 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974047 | AAAAATAGTCATCAG[A/G]ATTTTCTATCTCCAT | 9886 |
rs757798879 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980950 | ATGGTTTATAATTAG[A/G]TGGCTAATTAAAAAG | 9886 |
rs757817951 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934182 | ATTATGTGAAATTAA[C/T]ATCTACTCTTGACCT | 9886 |
rs757830211 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946364 | ACTGCCCTGGCAGCT[-/A]AAAAAATAGGGTAGA | 9886 |
rs757850098 | snp | C/T | 1.66172e-05 | 0.00288242 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888691 | TCCTCTGGGTCGACA[C/T]TCAATATCCGCCCCT | 9886 |
rs757850981 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991726 | ATGAGCCACCGCACC[C/T]GACCTTCCCTCAGTC | 9886 |
rs757857926 | snp | C/T | 3.47887e-05 | 0.00417051 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910851 | GAAAAGGAAATTGCA[C/T]TCAAGCTCAACCACG | 9886 |
rs757872753 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925472 | AATAAATGCCTATAT[C/T]GAAAAAGTAGAAAAA | 9886 |
rs757879521 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945159 | CAACCGGGTGCCTGC[C/G]ATCAGGGAGCTTTCA | 9886 |
rs757879941 | in-del | -/AAG | 1.6599e-05 | 0.00288084 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911557 | TTTATGAAACTCTGT[-/AAG]AAGAGAGTGAACACC | 9886 |
rs757932076 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905405 | CAGCAAGCCAAGATC[A/G]CGCCACTGCACACCA | 9886 |
rs757964482 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912266 | GGAATCTCACGCTGT[C/G]ACCCAGGCTACAGCA | 9886 |
rs757989780 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961348 | GTACAATTCTGGATG[C/T]ATTATGTGACCTTGC | 9886 |
rs758018929 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962420 | ATTTAACAGTAACCA[C/T]TTACAGGTTTGTCTC | 9886 |
rs758022832 | snp | A/C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994555 | TACTTCAGTCTTGAA[A/C/G]TATCTGCATGATGTT | 9886 |
rs758043909 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975089 | AATTTACAATAAAAA[A/T]ATGTCCATCAAGCTA | 9886 |
rs758053522 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884632 | ATGTGGTACTTATAC[A/G]CAATGGGATACTATA | 9886 |
rs758056325 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888398 | CCTTTTCCTTTTCAT[C/T]CAGTTGTCCCGTATA | 9886 |
rs758110348 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899020 | CTACCATCATAGTAC[A/C]AATATCATAGGGGTT | 9886 |
rs758141422 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934135 | AACAAGGAAATAAAA[C/T]ATCTTTGTGTGTGAG | 9886 |
rs758153466 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925180 | TATAAGCTTCCTGAG[A/G]TCTCTCCAGAAGCTG | 9886 |
rs758160917 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896472 | GGGGTAAAAAGCATA[A/C]GAATTCGAGAATGCA | 9886 |
rs758215601 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937473 | TCTCTGGAAATATTT[C/T]TTAGTTATCTGGCTG | 9886 |
rs758261342 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954736 | TTTTGAAATTACCCA[A/G]AAAGTGAATTTAATA | 9886 |
rs758280762 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900302 | AGAGAGGATGGTGAC[C/T]CTGCTGAGCCTGGGA | 9886 |
rs758295039 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943270 | TGCTGGGGATGGAAA[C/T]GGTGCAGCTAACAGT | 9886 |
rs758353422 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955494 | AGAATGCTTCCTTCT[C/G]ATTGAGCAGGGTAAT | 9886 |
rs758356363 | snp | A/G | 9.88419e-05 | 0.00702931 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888987 | GGGTGCCTGAAGTAA[A/G]GGTTTCTGGACTTTC | 9886 |
rs758358638 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876547 | CAGTTTCAAAAATAA[A/G]TAAAAATGTATCCTC | 9886 |
rs758367040 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985493 | CCTTGTATATGGCCA[A/T]GACTTTTCAGAGTCC | 9886 |
rs758372328 | snp | A/G | 4.94254e-05 | 0.00497094 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911421 | AGCAGCTGATACTGC[A/G]TGAGTGTGGTGTTGC | 9886 |
rs758375261 | snp | C/G/T | 1.65781e-05 | 0.00287902 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888739 | TTCTCTTTCTCACAG[C/G/T]CTCCTTCACTCCCAT | 9886 |
rs758382974 | snp | C/T | 3.62056e-05 | 0.00425459 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60871651 | AAGTATTCCTGGTTG[C/T]CTGGTGAAGGAAAGA | 9886 |
rs758399490 | in-del | -/TG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937446 | GCAAAAATTTTCTAC[-/TG]GCAATAATATTCTCT | 9886 |
rs758425290 | snp | A/G | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874722 | AGCTGGTGCCTTAGG[A/G]GACAATGGGACTGGC | 9886 |
rs758442553 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891922 | ATGCTATTCTCATAA[C/T]AGTGAGGAAGTTCTC | 9886 |
rs758457599 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964901 | ATATCTAATGTAATC[C/T]TACCTTATAGGCAGA | 9886 |
rs758469215 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917681 | CCTCTCCAACAGCCC[A/G]CCTCTTAATACAATC | 9886 |
rs758492448 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964988 | TAAAACAAAGTCTCT[-/G]GAAATAAACCCTCTG | 9886 |
rs758505005 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882331 | GCTTATAATTAGAGG[A/C]AGTCTCATAGAGAAT | 9886 |
rs758623739 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994076 | TGACTCAAAATATTA[G/T]AAATTATTGCTATGT | 9886 |
rs758651465 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880265 | GAGAGTGAGAGACAG[-/AG]AGAGAGAGAGAGAGA | 9886 |
rs758654473 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943739 | GCGGCTGTGCGGGCG[C/T]TCCTAGAAATCTCTT | 9886 |
rs758661809 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911521 | CAACGTTGGGTCTTT[C/T]GTAGTCCATGTCAGC | 9886 |
rs758676460 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951533 | TCACATGTGGGTGAC[A/G]TAAGCCATTAAACAC | 9886 |
rs758698960 | in-del | -/TATGTG | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912210 | GTGTGTGTGTATATA[-/TATGTG]TATATATATACACAC | 9886 |
rs758720043 | snp | A/C/T | 6.69628e-05 | 0.00578598 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911010 | AGGAGAGAGAGAGAG[A/C/T]ATCTGTGCTCGGTGT | 9886 |
rs758728689 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988837 | GTTAAGAATTCATTG[C/T]ATCCTCCTCTTCTAC | 9886 |
rs758745034 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000107 | AATTTTAGACTCAGG[-/A]AGCATTTTACAAATC | 9886 |
rs758760571 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928137 | TATAATCTCACCGCA[C/G]TTAAAATGGCTTTTA | 9886 |
rs758804260 | snp | C/T | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877953 | ATCTGTTTGCCAAGG[C/T]AATTAATTCCAGCGG | 9886 |
rs758804604 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925679 | TTTAGCCAGACTAAG[-/A]AAAAAAAAGAAGACC | 9886 |
rs758864619 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873991 | TTTCCCCCTTTTGCA[C/T]CAGAGCAATCTCCTC | 9886 |
rs758905253 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940078 | GTGCTGTTATAGAAT[G/T]TGACCTATTTTGTAA | 9886 |
rs758946925 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970047 | AATCATTACTCAAAG[A/C]CTGTATTTCCAGTGC | 9886 |
rs758984422 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982741 | CTGATGAGGAAATTG[A/T]GACTCCCAGAGACTT | 9886 |
rs758995253 | snp | C/T | 1.69129e-05 | 0.00290795 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878085 | TACAAAAAGCTAAAT[C/T]CTGCTGCAGAAAGCA | 9886 |
rs759034678 | in-del | -/AAAC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959570 | GCTGAAACAAAAATG[-/AAAC]AAACAAACAAACAAA | 9886 |
rs759037657 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906720 | TAAACTGTAGTTGTT[A/G]TCACTGTCAGCAACA | 9886 |
rs759050990 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977957 | GATATGCACAGGAAA[G/T]AAATAGATCACTTAT | 9886 |
rs759091750 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948259 | TACTACCATCCCAAG[A/G]GAACTCTATTTTCAA | 9886 |
rs759133028 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964863 | GGATTAAACTTCAAC[A/C]TTCTTTATAAAAATT | 9886 |
rs759133913 | snp | A/T | 1.68244e-05 | 0.00290033 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888588 | AACTGCACCCTCGGC[A/T]TCCAGCCCCAGAGCC | 9886 |
rs759151978 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881165 | CTCTCTTGCCTGCTG[A/C]CATGTAAGATGTGCC | 9886 |
rs759193323 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869740 | TTCCACATCTTGTCT[C/G]CTTTCTCCTTCCATC | 9886 |
rs759262815 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911479 | TCCCCACGGCATTGT[A/C]ACCCACGACCACACA | 9886 |
rs759314716 | snp | A/G | 6.7603e-05 | 0.00581351 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877887 | GACAGACACTGCATG[A/G]CCCTGAGTCATCATC | 9886 |
rs759327610 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936140 | GATTCCCATCATGGA[C/T]GAATGAGTAGAGTTC | 9886 |
rs759328728 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958298 | TGTCCAATATAAAAA[C/T]GTTAAACTCTCATTT | 9886 |
rs759392677 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904187 | CCTGGCCTCAAGTGA[G/T]CCACCTGCCTCAGCC | 9886 |
rs759397418 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939446 | ATATCCCATCCACTG[C/G]AGTGACTGCCTCTTG | 9886 |
rs759399432 | in-del | -/GTG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905310 | AAAAATTAGCTGGGT[-/GTG]GTGGTGGTGGGCACC | 9886 |
rs759478642 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906195 | TTCTGAATGTTTTTG[C/T]TAAATGATTTGGGGA | 9886 |
rs759481877 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913941 | TAAGTCCTCAGTGCC[A/G]TAACTGACACACTGA | 9886 |
rs759513206 | snp | C/T | 1.65023e-05 | 0.00287244 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878019 | AGAGATAATCCAATA[C/T]TGCTTGCATTGATAT | 9886 |
rs759523005 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960999 | TAAGTATGGGGATTC[A/G]CTAACTCTATCTGTA | 9886 |
rs759527689 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917084 | AGACCCATGTCAGAC[A/C]TTTGATTTTCAGAAC | 9886 |
rs759549632 | snp | C/T | | | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944550 | AGGGGAGAGTCTGGG[C/T]CATCTGTGTCCCCGT | 9886 |
rs759551212 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988423 | CCCAGGTAGTGAGCA[G/T]AGTACCCAACTGGTA | 9886 |
rs759554905 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002552 | TTTTGCATGAGCTTG[C/T]GTAATGAAGGGCTAG | 9886 |
rs759582928 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961552 | GTCACATGGATCTAG[A/G]TTCAGAATGAAAGCT | 9886 |
rs759650388 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932445 | TCAGTTTGCAAAAAG[C/T]CATCAAGCTGTACAT | 9886 |
rs759671666 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974588 | TCTTGGGCATGGGAT[A/T]TGAGTTTAGACTTGT | 9886 |
rs759679361 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888450 | AAAAGGGCCTGGCTG[A/G]ACTGAAGCGTCCATC | 9886 |
rs759703892 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931231 | AAGTATACAATTCAG[C/T]GGTGTTTATGATATT | 9886 |
rs759775764 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873259 | CCAGCTTGAGAGAAC[A/C]AATTGTGTGCATTTC | 9886 |
rs759783594 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883955 | TGTCTCAGTAATGAT[A/G]CTCCAAAACACCTTT | 9886 |
rs759786799 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895694 | CAGGCGCAAGCCACC[A/G]CGCCCGGCCCAAGAT | 9886 |
rs759797986 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909008 | ACAGAACCAAATGTT[A/G]CAGACAAGGGAGCAG | 9886 |
rs759844788 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991163 | ATATGCATACTCTTC[A/C]CCCTTGCCAACCCAT | 9886 |
rs759874828 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889062 | CGCTGCTCGGATTGC[A/G]TTGTCAAACACATCC | 9886 |
rs759903938 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925673 | ACAAATCTTTAGCCA[C/G]ACTAAGAAAAAAAAG | 9886 |
rs759907146 | snp | A/G | 1.66247e-05 | 0.00288307 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886238 | TGTCACGTCTGCCAA[A/G]GGATTGAGGAAACAC | 9886 |
rs759920706 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996464 | TTCCAGACCTTTCCA[A/G]CCCAGAGAAAATAGC | 9886 |
rs759921788 | in-del | -/T | 1.69502e-05 | 0.00291115 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871464 | GGTTTCTGTTTTTTG[-/T]TTTTTTTCTCTTCCT | 9886 |
rs759926673 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953745 | CTTGATGTTTCTTCT[C/T]GATAAAACAGTTGAG | 9886 |
rs759949096 | in-del | -/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944752 | CCAGCTGCTGACTAA[-/G]GGGCTGCATTAGCCC | 9886 |
rs759999991 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933832 | TGTGTTATAGGAGTA[-/C]ACTCATTGTTATATT | 9886 |
rs760030884 | snp | G/T | 1.68485e-05 | 0.00290241 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871462 | TTGGTTTCTGTTTTT[G/T]GTTTTTTTTCTCTTC | 9886 |
rs760032547 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903667 | TGAGAAACAGGCCCC[C/T]GGGTCAGACTATGGG | 9886 |
rs760071925 | in-del | -/GA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950300 | AAAAAATCTACATTT[-/GA]GAGAGAAATTTATTT | 9886 |
rs760092265 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912026 | ATATCTGTTGTTGAA[A/G]AGCAGTTTTCTATAG | 9886 |
rs760098499 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876953 | CAACAAATATTTATC[A/G]AAAGCTAATATGCTC | 9886 |
rs760124558 | snp | A/C/T | 0.000115395 | 0.0075951 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886184 | GCTACAGATCAGCAG[A/C/T]GGCTTGTGGGCACTG | 9886 |
rs760157445 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942672 | CAGTGACTCTCTTAG[G/T]CATCTACAAGGTTAC | 9886 |
rs760164161 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993691 | TTTTATATTGCTCTA[C/T]GGTGTATATTTTATT | 9886 |
rs760168385 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984963 | AGGTCTCCTTAAGGA[C/T]TTCTACTTTATTATG | 9886 |
rs760239780 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918997 | GTGATTCACCCACCT[C/T]GGCCTCCCAAAGTGC | 9886 |
rs760255424 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949481 | AGGTATTACTCAGAC[C/G]AACTCTTCAGATCTC | 9886 |
rs760260738 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969580 | GTAAAGGGAATTTAT[-/AG]AGAGACAGATTATGG | 9886 |
rs760275114 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899470 | AGCTACCGCGCTACA[C/T]GGGAGGTCTCTGGGA | 9886 |
rs760284512 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936195 | TTTTGTCTTACTGAT[C/T]AACATAAAGGAAAAT | 9886 |
rs760285210 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998066 | ATTATCATTCTGAGC[G/T]TCAGTTTCCTCTGCC | 9886 |
rs760305868 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967900 | CAAAATGTCCCTGTT[C/G]TGGCTTAAATTTACT | 9886 |
rs760315476 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911489 | ATTGTCACCCACGAC[C/T]ACACATTTGATAGTT | 9886 |
rs760340264 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930353 | TTGTGAAATATTTCA[A/G]TCTCTGTGCTTGGTA | 9886 |
rs760344352 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930881 | ATCCATTATTCCCTC[A/C]GACAAATAAACGAAT | 9886 |
rs760371169 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959157 | TGGTAAAATGTAACA[C/T]CCATCTGTGACTAAA | 9886 |
rs760372764 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876206 | AAAGCATTGTCACTG[C/T]AGAAACTGATTTTTA | 9886 |
rs760406726 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887076 | GTATTTCATAGCTTT[A/T]AAAAAAAAAAAACAG | 9886 |
rs760413056 | snp | A/C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934242 | GAACTGCCTTTCATA[A/C/T]GGTAGGGAACAGGCT | 9886 |
rs760424813 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971978 | GAAATGCAAATCAAA[A/G]CCATAATGAGATACC | 9886 |
rs760426714 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918530 | GACAGGCGCACTTCA[C/G]TGTAGGGCCACTAAT | 9886 |
rs760430432 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907757 | CAAATCCAAAAGAGC[A/G]AATAGAAATCCAGCT | 9886 |
rs760439934 | snp | A/C | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888770 | TTGGGGATTCTTCAC[A/C]TTCCATTAAAAACAG | 9886 |
rs760458626 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925876 | AGAAATACAAAATCT[A/G]AATAGACCAATAGCA | 9886 |
rs760494688 | snp | C/T | 3.29913e-05 | 0.00406135 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892954 | ACATGATTTAGGGAA[C/T]TGGGATTAGCAATCG | 9886 |
rs760498563 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881613 | CTCACCCTCAGTCTC[C/T]TCATCCGTTACATGG | 9886 |
rs760509869 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869873 | GGGCCTCTCCTAAGA[C/T]CTTCTATCTGGTGTT | 9886 |
rs760527725 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929998 | GTAAATTGTTGTCAA[C/T]CAAATTCTCTGGCTG | 9886 |
rs760554149 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958493 | AATTGAAACACTATA[C/T]AGATATGGATTTCCA | 9886 |
rs760558932 | snp | C/T | 7.13343e-05 | 0.00597177 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893040 | TTGCCTTTTAACAGG[C/T]TTTTTCTTTTACCAT | 9886 |
rs760575712 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902815 | TGGCATTTGTTATAA[A/G]ACTATTTCCTTGTCT | 9886 |
rs760592921 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960321 | CCAGAACCCCCTATT[G/T]ATTATGCTGGCGAAT | 9886 |
rs760598477 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907323 | AATGTGGACATTTCA[G/T]TTTTATAAGAGCTCC | 9886 |
rs760628782 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922116 | TAAGGGTCTCATAAA[G/T]TTCTCATCCACTTTT | 9886 |
rs760656529 | snp | A/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882807 | GTTCAGAAAGGGAAC[A/T]GGGGGCTTTTTAACT | 9886 |
rs760673769 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907514 | TAAAGTAGGTGGTGG[-/A]AAAAAGGCCATAAGA | 9886 |
rs760678444 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896833 | AATCTGAAATAAATC[A/G]AAATGTTGAAACAAT | 9886 |
rs760679976 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933761 | AACAAAAATAACTTT[A/C]GAAGTCCAAACACAG | 9886 |
rs760683129 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988697 | CATTTTCTTTATTCA[A/G]TCCACCACTGATGGG | 9886 |
rs760724193 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940387 | GGGGAACAGAAGAGA[A/G]AGAAGCCTGTTAATT | 9886 |
rs760736633 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989666 | AGTGACGTCCACTTT[A/G]CCCCTACTCTGGGTA | 9886 |
rs760791998 | snp | C/T | 1.65209e-05 | 0.00287405 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875026 | GGCTTTGGTCAACTC[C/T]TGAACGGCATGCTGT | 9886 |
rs760823262 | snp | G/T | 6.60698e-05 | 0.00574722 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886190 | GATCAGCAGCGGCTT[G/T]TGGGCACTGATGGCT | 9886 |
rs760873281 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962093 | GATTACAGGCCTAAG[C/T]CACTGTGCCTGGCCC | 9886 |
rs760882621 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993582 | GAATTTCATGGCATA[A/T]ATTTTCAGTATGAAT | 9886 |
rs760894031 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949956 | TGTGTAGGTTTACCT[A/G]AAGTCCTTTCTGTGT | 9886 |
rs760895478 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985048 | GAGTTATCTATAATT[C/T]AGCTTTCCCACAAAT | 9886 |
rs760903454 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904025 | TATAGTACAGTTGTG[C/T]AATCCTAGCTCACTG | 9886 |
rs760909226 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885123 | GCACAGTATGGTGAC[C/T]ATGGTGGACAATAAT | 9886 |
rs760929366 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873696 | TTTCAAAAGACCCCA[A/G]ATTCCAAGTGTGAAC | 9886 |
rs760953767 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928076 | TATGAAAAAATGCTC[A/G]ACATCATTCGTCATC | 9886 |
rs760988598 | in-del | -/CACT | 1.64866e-05 | 0.00287106 | frameshift-variant, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910951 | AAAGCCTGAGAGAAA[-/CACT]CACTTCATCAACAAC | 9886 |
rs761003072 | snp | A/C | 1.67019e-05 | 0.00288975 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886253 | GGGATTGAGGAAACA[A/C]AACCATGAGCCAACT | 9886 |
rs761003485 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981782 | ATAAGTTACTTTTTT[A/T]TTTTAACACGGAGTT | 9886 |
rs761007147 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936071 | ACTATGAATAGTACA[C/T]TTGAAAAATATTCTT | 9886 |
rs761008230 | snp | A/C | 1.9214e-05 | 0.00309945 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889236 | TGTTTTAGGAAAAAA[A/C]CAGTAACAAGGGCCT | 9886 |
rs761048896 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998885 | GCAGCAGGAAGTACC[A/G]GACTGTAGTGGTTCA | 9886 |
rs761055952 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878270 | TGGAGCTGCCTGACA[C/T]AGCCTGATGTGGAAT | 9886 |
rs761056470 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955308 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG | 9886 |
rs761103738 | snp | C/T | | | nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60985914 | GCTTGATGAAGAGGC[C/T]TCTTTCATGTGCTTC | 9886 |
rs761180589 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877225 | AAGTTAAGCCAAGTT[C/T]CCCTTTTTTCTCTTT | 9886 |
rs761185885 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995357 | ACTGGCCTGGGGGAG[A/G]AACCATCAGAGATTG | 9886 |
rs761200757 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965551 | TTGTAAGAGAATTAA[A/T]TGGTGTGCCTTTTGT | 9886 |
rs761233951 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945878 | GGGTGATCATTTACT[C/T]GGCATAAAACTGACT | 9886 |
rs761244171 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900215 | AGAGTGGGAGAGGAC[C/T]GGGAGGGTCAGCGGA | 9886 |
rs761310119 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932794 | GATATACTAAGCACT[C/T]ATTTGAGAAAGCTAA | 9886 |
rs761319399 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974862 | ACATTAGTTCTCTTT[C/T]CTGTGGGGTAGAGAA | 9886 |
rs761347316 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968131 | TTTCTCTCCTACCTC[G/T]TCACCAGCCAATTCA | 9886 |
rs761353740 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878531 | TGACCAGCTTGATTT[A/C]GAAATTCTGTCAGTA | 9886 |
rs761381017 | snp | A/C | 1.67475e-05 | 0.00289369 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878064 | GGAGATACACCTGAA[A/C]TGTTATACAAAAAGC | 9886 |
rs761383014 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888923 | TTGTCCCCATGGAAG[A/G]ACACTCTGGAATTTT | 9886 |
rs761386067 | in-del | -/TG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892280 | TTAAAAAGTAGTAAC[-/TG]TTTGTTTTGCAACTA | 9886 |
rs761402369 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938020 | AAGTTGCATAGTTAA[C/T]GAAATGCCAGAGTTT | 9886 |
rs761422260 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969587 | GAATTTATAGAGAGA[C/T]AGATTATGGCTCAAT | 9886 |
rs761473210 | snp | A/G | 1.65211e-05 | 0.00287407 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888807 | AAATTTGGAAGAAGA[A/G]GTAGCGAGGTAAATT | 9886 |
rs761493842 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000856 | CCTTTTTACAGCCCG[G/T]GGCTTTCACGGCTAA | 9886 |
rs761496575 | in-del | -/AC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997066 | AGCATGGTTATGTAC[-/AC]ACACACACACACACA | 9886 |
rs761572268 | snp | A/C | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943219 | CTTGTCCAAGTCTAA[A/C]TATTGACATCGCTCC | 9886 |
rs761577600 | snp | A/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910944 | GTATCCCAAAGCCTG[A/T]GAGAAACACTCACTT | 9886 |
rs761587543 | snp | A/G | 3.30819e-05 | 0.00406692 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886103 | CTATGCTTTTAGGAA[A/G]GCACGTACCTCACTG | 9886 |
rs761603698 | in-del | -/CCTA | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945784 | TGGAGTTACCAAGGC[-/CCTA]CCTAGTCTTTGATAT | 9886 |
rs761616825 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907362 | ACTCTTGAGTTGAGC[A/G]ACATCCCTTTAAGAA | 9886 |
rs761626705 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960579 | TTGGATGGAATATTA[A/G]TACTGGAAATATTCT | 9886 |
rs761631048 | snp | A/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884843 | GGATTAGGGGGTGAA[A/T]GGGGAAAGGAAAGCC | 9886 |
rs761661476 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968748 | GTAGACAAACATCAT[C/T]TCCTTTCCCTGAAAG | 9886 |
rs761667532 | snp | G/T | 1.76487e-05 | 0.00297053 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910836 | CCCGCTGCTGGTTTT[G/T]AAAAGGAAATTGCAT | 9886 |
rs761695282 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908918 | TCCTGAAGCCCCTCA[A/C]TGTTGCTCAGAGAAT | 9886 |
rs761739788 | snp | A/G | 1.67787e-05 | 0.00289639 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888572 | AAGTCTGTGTCTCAG[A/G]AACTGCACCCTCGGC | 9886 |
rs761746188 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911712 | ACTAAGCCTAATTGA[C/T]ACTCAAGTTTTCTTT | 9886 |
rs761763046 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60882915 | AACATTTATTGAACA[C/T]TTGTATGTTCTAGGC | 9886 |
rs761778076 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899257 | CTCCTGGTCAACGAA[C/T]GCAGGAGGCACTGAA | 9886 |
rs761814548 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870316 | AATTAGATTCCTTTC[C/T]GTGTAGGAGAACGCA | 9886 |
rs761872807 | snp | C/T | 1.68966e-05 | 0.00290655 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888219 | CCACTCACCCGAGAA[C/T]GTTCCCTTGCTGAGA | 9886 |
rs761890248 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923272 | GATAAACATGCTATA[G/T]AAAACAGCAGAAAAA | 9886 |
rs761891832 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980300 | AAGAGAGAATTCAAT[A/G]CAAAAATCAATAAAT | 9886 |
rs761929259 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872667 | TTTAAGGAAGCCTCC[A/G]CAATGGAATACTTCG | 9886 |
rs761941420 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873748 | GCTGATTCGACTGCA[G/T]TAGATGTCTATTCTC | 9886 |
rs761960412 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910713 | GGCACGCTTCTTTTC[C/T]TGACATCAGGAAACA | 9886 |
rs761963332 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928287 | ACTAAAAATCAAACT[A/G]TCTTATGAGCCAGTA | 9886 |
rs761963535 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951961 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 9886 |
rs761974890 | snp | A/G | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892890 | CCCAACAAGGATAAC[A/G]GGTGTTCGAGGGCAA | 9886 |
rs761984741 | in-del | -/A | 0.000551672 | 0.0165991 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889229 | CAGCCTTGTTTTAGG[-/A]AAAAAAACAGTAACA | 9886 |
rs762014552 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951431 | GTATCCTTAGCTCTG[C/T]AAATATTTATGCCTA | 9886 |
rs762021012 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982599 | CTCAACCCCTCCAAT[A/C]GTTATAGCCAAAACA | 9886 |
rs762029425 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874503 | GCAAGTCTGTATTGG[G/T]ATTATGTTATTACAA | 9886 |
rs762036694 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974987 | ACCTCTGTATGTGTG[A/G]CTGAGAGCTGTATGA | 9886 |
rs762038663 | snp | C/T | 6.5912e-05 | 0.00574035 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911509 | ATTTGATAGTTTCAA[C/T]GTTGGGTCTTTCGTA | 9886 |
rs762051948 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990443 | CTCTCAAACAGGCAG[A/G]ACGACAGACAGAACC | 9886 |
rs762076215 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983415 | TCTTATAGTTATAGT[A/G]TAATCCCATGTTAAG | 9886 |
rs762090844 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995938 | CATAGTATTTATGCA[A/C]CATTAATTGAATATT | 9886 |
rs762117002 | snp | A/G | 1.67203e-05 | 0.00289134 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886260 | AGGAAACACAACCAT[A/G]AGCCAACTTTGCTGA | 9886 |
rs762133389 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912726 | AGGAAGAAAAAAAGC[A/G]CCTGCCAGCTTGGTC | 9886 |
rs762158314 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940694 | TAATCTCTCCCTGTT[A/G]GGTTGAAATTCTACA | 9886 |
rs762163733 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901373 | AAGTGTTCTGTAACC[A/G]TTAAGTGCCAATTAT | 9886 |
rs762185361 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945960 | CGAGGCGCGCGGATC[A/G]CGAGGTCAGGAGTTC | 9886 |
rs762206703 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906209 | GTTAAATGATTTGGG[A/G]AAAACATGCCAAGAT | 9886 |
rs762209036 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946926 | CAAGAAAATAAGTTG[G/T]TATCAACAGTAATTC | 9886 |
rs762349950 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963352 | GAATTTAATCAGCAA[A/C]TATTCTGACTACAAT | 9886 |
rs762373567 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916147 | CTTCGCCCAAAAGAA[C/T]GTGGTGGAGGTGATG | 9886 |
rs762409574 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896943 | AGCTCAGCTGCATCA[C/G]TTTTACTTCAGATTT | 9886 |
rs762436206 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922188 | GGTGAGTCACTACTT[C/T]GCTGGAAAAGAAAGG | 9886 |
rs762487006 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903861 | ATTTACGTTTTCAAC[A/G]AGACTAACTTAAAGT | 9886 |
rs762495476 | in-del | -/TTTG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958607 | GGTTTATGTTGTTGT[-/TTTG]TTTGTTTGTTCAAAA | 9886 |
rs762503584 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946109 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 9886 |
rs762531638 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958010 | GACACCACTTGTGAG[C/T]GTCTGCCAGAACAGA | 9886 |
rs762551645 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995631 | GATCAGAGTAAATTA[C/T]CTGAATTATCCATAA | 9886 |
rs762566093 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957488 | ATGGTGCAGGACTGT[-/A]GTCTTCTGAGGGACT | 9886 |
rs762573167 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878367 | CCCTCATGCCAAGCA[C/T]CTTATAATACTCTAC | 9886 |
rs762579660 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947149 | ATCATATCAAATAAC[A/G]CCTGTAATCACTGTC | 9886 |
rs762583086 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936488 | ACCAGGTCATCACCG[C/T]CTACATCCCTCCTAT | 9886 |
rs762590924 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987365 | CATCCCCATCCTCTC[C/T]TGAATTTGCCTTTTT | 9886 |
rs762619294 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879928 | AGGCATGACTGCTTC[C/T]GTTCTGAACATGTAC | 9886 |
rs762641772 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988396 | AGGTTTGGGGTACAA[A/C]TTTTCCTGTTACCCA | 9886 |
rs762692456 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906632 | AGCCTATTTTGCAGG[C/G]TCACCACAAGAGTGA | 9886 |
rs762737546 | snp | C/T | 1.7151e-05 | 0.00292835 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871448 | GATCAGATTACCGAT[C/T]GGTTTCTGTTTTTTG | 9886 |
rs762763004 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899707 | CAGGCATTCTTCTAG[A/G]CATTGGGGATAGAGT | 9886 |
rs762788485 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910331 | TTTCTCCTTTTTAAA[A/C]AAATAAACGTTAGTG | 9886 |
rs762801403 | snp | A/C/G | 9.92973e-05 | 0.00704555 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888491 | TCATGGGCCCCATCC[A/C/G]CTTTGAAATGGGGTT | 9886 |
rs762804726 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923381 | TATAAGTAGTTAATG[A/T]GACAAGATAAAGACC | 9886 |
rs762821736 | snp | C/T | 1.70061e-05 | 0.00291595 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877878 | GACAAATATGACAGA[C/T]ACTGCATGGCCCTGA | 9886 |
rs762829289 | snp | C/T | 1.65329e-05 | 0.0028751 | splice-acceptor-variant, downstream-variant-500B, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875043 | GAACGGCATGCTGTT[C/T]TGGGGAAGAGAGAGG | 9886 |
rs762869242 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890317 | TCCTCACATTTTAGT[C/T]CACAGTCCTCACTGC | 9886 |
rs762889729 | in-del | -/TT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920956 | TTTGTTTTTTTTTTG[-/TT]TTTTTTTTTTTATGA | 9886 |
rs762947905 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972272 | ATTCACAATAGCAAA[G/T]ACTTGGAACCAACCC | 9886 |
rs762997628 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875899 | GTGAGGGTACAGCCT[C/T]GGCTCAGCATTTCTA | 9886 |
rs763041915 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969616 | ATTAGGATTTTCTAT[C/T]AATCAGAACAGCCTG | 9886 |
rs763080753 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909897 | CAAACTCTTTCAGCA[A/G]TTTATTCATTATTTT | 9886 |
rs763093603 | snp | C/T | 1.75832e-05 | 0.00296501 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893033 | GCTTGTATTGCCTTT[C/T]AACAGGTTTTTTCTT | 9886 |
rs763097462 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930256 | GGCAAATTAATCTGT[C/T]GGAGCCTCTATATTC | 9886 |
rs763100247 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984710 | TAATTTGGGACTTCA[A/G]TAAATTTAAAATCTT | 9886 |
rs763103046 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959304 | AACGGACCTACAGTA[C/T]GGCACTCTCAGGAAA | 9886 |
rs763112334 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893160 | TCATGCAAACAGCCT[G/T]ATAAGCCCCCACATT | 9886 |
rs763157098 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885330 | AAAAGTAAAACAACA[A/G]GAAAGACAAAGACAC | 9886 |
rs763165530 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993374 | ACCAGAAATATATCT[C/T]TTTATTCCTTATTAC | 9886 |
rs763179324 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898446 | AAGGAATGTGTAACA[C/T]GTGGCTTTGGAAAAT | 9886 |
rs763183117 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892941 | CCACATGCTTTTCAC[A/G]TGATTTAGGGAATTG | 9886 |
rs763208932 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894368 | GTAGATGAATGTATT[A/C]ATCTGAATGTTCAGA | 9886 |
rs763244365 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934920 | AAAGGATCAACAGCC[A/G]TGGGCATGTTATATG | 9886 |
rs763263355 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977935 | ATTAATCATTTACCC[A/G]TTAACTGATATGCAC | 9886 |
rs763267014 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963503 | ATTTAGACAGCAACA[G/T]TACAACAGAAAGCCT | 9886 |
rs763268687 | snp | A/C/G | 9.91943e-05 | 0.00704194 | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872154 | GAGAGGTGAGGAGAG[A/C/G]TGGATGAATGGGGGC | 9886 |
rs763280439 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913784 | GATGTGAGTTTGAAT[C/T]CTAGCTCCCCCATTT | 9886 |
rs763301239 | in-del | -/GGGAATTGTATGCAACA | 1.68377e-05 | 0.00290148 | frameshift-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888599 | GGCTTCCAGCCCCAG[-/GGGAATTGTATGCAACA]AGCCTCCACCAGGCT | 9886 |
rs763301456 | snp | A/C/T | 0.000131847 | 0.00811833 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888359 | TCTCGAGGACCTCTG[A/C/T]GATCTGAGCCAGGCC | 9886 |
rs763302732 | snp | C/T | 6.58903e-05 | 0.00573941 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889047 | CCTGCGGGAAATCAG[C/T]GCTGCTCGGATTGCA | 9886 |
rs763309429 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990399 | AAGAATCTTTTTGAG[-/A]CAGATGCAAGACATG | 9886 |
rs763327695 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931123 | CCTGCCATTTTCTAC[C/T]TTTCTTTTGATTCCA | 9886 |
rs763336981 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936027 | AATGGAGATTAAACT[G/T]TAAAGTGTGCTATAT | 9886 |
rs763348869 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870643 | ACTGAGAGATGTAAA[A/C]CCTAATACAGCAATC | 9886 |
rs763354350 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898088 | TTGTTCCATGGTAGG[A/G]TCCCACCTCTTTATA | 9886 |
rs763363541 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964469 | TTACAATTACTTCAA[A/G]GATTGCTGTATAACC | 9886 |
rs763396863 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954540 | ATAGAGGACACCCCA[C/T]TACATTCAAATATCC | 9886 |
rs763436960 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952235 | CTGTTCTACTGTGAT[C/G]ACTGTCAACACTGAT | 9886 |
rs763441931 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966127 | AGAATTTGAAAGGAA[C/T]AATGTCTTGAAAAGA | 9886 |
rs763444317 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913021 | AAAGAAACTGTTCAG[A/T]GTAAAGCCTAATACA | 9886 |
rs763449787 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999614 | AGGAATCAATAATTA[A/T]TCCAAGTAGGTATAC | 9886 |
rs763511166 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913396 | CTTATCCTGAACATC[C/T]TGGGTGGGGAAAAAG | 9886 |
rs763537625 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978220 | TTTTAATGGCGTCTT[C/T]AGAATTCTGCAAAGC | 9886 |
rs763544970 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994816 | ATCTCATAAGTTTAT[A/G]AGCCAAGTAAATTCT | 9886 |
rs763562126 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996829 | TCCAGATTTAACTAG[C/G]CATCCTGTATTTGAT | 9886 |
rs763571807 | in-del | -/C | 1.64985e-05 | 0.0028721 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871698 | TGCGGTTCATTGATG[-/C]CTTTTATGTGCTAGG | 9886 |
rs763599382 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996242 | TTTCCAACATGGGCA[A/G]TCTAAACCCTTCAGA | 9886 |
rs763614717 | snp | C/T | 3.31961e-05 | 0.00407394 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877921 | ACCTGCAAGTGCAAC[C/T]AAGTGTGGCAGGCAA | 9886 |
rs763636294 | snp | G/T | 1.65499e-05 | 0.00287657 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888785 | ATTCCATTAAAAACA[G/T]ATCATAAAATTTGGA | 9886 |
rs763647139 | snp | C/T | 1.65965e-05 | 0.00288062 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878047 | TATCTTGTTTATGTT[C/T]GGGAGATACACCTGA | 9886 |
rs763679412 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898812 | ATGTTTAGTAGGAAG[C/T]AATATTTTAAACCAG | 9886 |
rs763703090 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955318 | AGTGCTGGGATTACA[G/T]GCATGAACCACCACA | 9886 |
rs763741279 | snp | A/G | 1.65154e-05 | 0.00287358 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888270 | TTTCCTTACGTGAAA[A/G]GCTTTCGTAATCTCC | 9886 |
rs763756411 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954348 | TTATTATAAAAATAC[A/G]GAAGATATAGCAGTC | 9886 |
rs763782612 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967988 | AGGAGAATTTAGCGC[C/T]GGAGGGAAAGAAGGG | 9886 |
rs763799489 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931812 | TGTTTTTCTGAGTAT[C/T]AGACACAGAAATTGA | 9886 |
rs763801286 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954999 | AGTCCACTTTGAGCT[A/C]CCCATACTTATTTGA | 9886 |
rs763815253 | snp | G/T | 1.64991e-05 | 0.00287215 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892956 | ATGATTTAGGGAATT[G/T]GGATTAGCAATCGAA | 9886 |
rs763818105 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985071 | CCACAAATTCAGATA[C/T]GCCCACCATCTTAAT | 9886 |
rs763863421 | snp | C/G | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888518 | GGTTGACTTGCATTT[C/G]CCTGTGCATGCCAAT | 9886 |
rs763876924 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881668 | AAAAGCTTTTTCTTC[-/T]TCACGGAAACTCTGG | 9886 |
rs763917304 | in-del | -/ATT | | | intron-variant, cds-indel | RHOBTB1 | GRCh38.p7 | 10:60885298 | TAACTATGTATAATA[-/ATT]ATTATTTGTCAGTTA | 9886 |
rs763932756 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919514 | CGGGAAAGAGATGCA[A/G]GGGCTGGGCTGGACT | 9886 |
rs763939374 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881402 | CCACATTTTACAAAG[C/T]GCTAAGTGCTCTAAG | 9886 |
rs763942407 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959222 | AGCAAGGGAAAGACA[C/T]GGCCACATATTTGCT | 9886 |
rs763950495 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907345 | AAGAGCTCCAGGAGA[C/T]AACTCTTGAGTTGAG | 9886 |
rs763990581 | snp | A/C/T | 3.61254e-05 | 0.0042499 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893046 | TTTAACAGGTTTTTT[A/C/T]TTTTACCATTATGGT | 9886 |
rs764035728 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988704 | TTTATTCAATCCACC[A/G]CTGATGGGCACCTAG | 9886 |
rs764049292 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936346 | TGAATTTATAATATC[A/T]AGTATTATAGAGTTT | 9886 |
rs764057556 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978316 | AAAGTTCCTGGCTGT[C/T]CACATCTCCAACCCC | 9886 |
rs764074933 | in-del | -/TTTT | 2.33801e-05 | 0.00341899 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871700 | CGGTTCATTGATGCC[-/TTTT]ATGTGCTAGGCCTTG | 9886 |
rs764086469 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989683 | CCCTACTCTGGGTAG[C/G]TTTCCAACTTTGGTG | 9886 |
rs764092342 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888371 | CTGCGATCTGAGCCA[A/G]GCCCACCAAATCCTT | 9886 |
rs764106323 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948815 | CAACAACTTTCTGGC[A/T]TCCTAAAGAGGAAGA | 9886 |
rs764136039 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870181 | TAATTTACAGAGAAG[A/C]AATGACTGACTGCCT | 9886 |
rs764181708 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939463 | GTGACTGCCTCTTGA[C/T]CCTTCCCTTAAAAGC | 9886 |
rs764258389 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910691 | CACAGTACTTCCTCA[C/T]TGGCAGGGCACGCTT | 9886 |
rs764260050 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928074 | CATATGAAAAAATGC[A/T]CAACATCATTCGTCA | 9886 |
rs764265813 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981791 | TTTTTTTTTTTAACA[C/T]GGAGTTTCGCTTTTG | 9886 |
rs764284344 | snp | C/G | 4.9467e-05 | 0.00497303 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886193 | CAGCAGCGGCTTGTG[C/G]GCACTGATGGCTCCA | 9886 |
rs764313355 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909401 | GAGCTGTTGAAATAG[C/T]CTCTAGATTCTAAAC | 9886 |
rs764323108 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932514 | TACTTTCTTAAAGTA[-/AAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 9886 |
rs764341563 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873740 | GGGGGCTTGCTGATT[C/T]GACTGCATTAGATGT | 9886 |
rs764390217 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995405 | CTCCAGAGCACCCAA[G/T]ATATCATTTCCAAAA | 9886 |
rs764392626 | snp | A/G | 3.31055e-05 | 0.00406837 | synonymous-codon, nc-transcript-variant, missense | RHOBTB1 | GRCh38.p7 | 10:60871605 | ATCTTCTTCCTTCAG[A/G]TACCACACAGGGGGC | 9886 |
rs764431740 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914120 | ACCAAGCAGTAACTC[A/G]CTGAAAATTAAAGAA | 9886 |
rs764461667 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921036 | CTCACTGCGACCTCT[A/G]CCTCCTGGGTTCAAG | 9886 |
rs764478450 | snp | C/G | 1.67206e-05 | 0.00289137 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886257 | TTGAGGAAACACAAC[C/G]ATGAGCCAACTTTGC | 9886 |
rs764480671 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871521 | CCAGAAGCACCACTT[C/T]CGTCTTGAGCGATGC | 9886 |
rs764499861 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894736 | TCTGAGGTTCAAAAT[C/T]ATACAAAAAGAATTG | 9886 |
rs764500839 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944837 | TACCTTCCTCCGCGA[C/T]TTGGCGGGAGGGGTC | 9886 |
rs764574174 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896088 | TAGTCAAAGAAGGCA[C/T]AAGACCTGCAGCTAA | 9886 |
rs764577246 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970213 | TAAAAAAATTGGTTA[C/T]TTGTGGTTACAAGTC | 9886 |
rs764584901 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991635 | ACGGGGTTTCACCAT[C/G]TTGGCCAGGCTGGTC | 9886 |
rs764652290 | snp | C/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883281 | TCATCTCTCCAGCAG[C/G]GTGTGCTAAACAGGT | 9886 |
rs764669077 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974885 | GTAGAGAAGGCATCG[C/T]GATGGCATGTATGGG | 9886 |
rs764687084 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895932 | TGCAGCTTTGATGCA[C/T]TTCTCCTTACCAACA | 9886 |
rs764687564 | snp | C/T | 1.68439e-05 | 0.00290201 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888596 | CCTCGGCTTCCAGCC[C/T]CAGAGCCTCCACCAG | 9886 |
rs764689756 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911490 | TTGTCACCCACGACC[A/G]CACATTTGATAGTTT | 9886 |
rs764696166 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927545 | AAGAGAATAGAGAAC[C/T]CAGAAAAAAATTCCC | 9886 |
rs764791596 | snp | A/C/T | 3.3064e-05 | 0.00406585 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886107 | GCTTTTAGGAAGGCA[A/C/T]GTACCTCACTGTTGG | 9886 |
rs764795684 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955550 | ATCCCAAACCACAGA[-/G]GAGTTGCTAGCTATC | 9886 |
rs764808789 | snp | G/T | | | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945070 | GTAGTTTTCATGCAT[G/T]CACATAAATGCTTAT | 9886 |
rs764824273 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915929 | TTTTACTTGAGCCAT[A/C]CATCCTTTTGGACAC | 9886 |
rs764825949 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932960 | ACCACCTGCTGTGGT[C/T]TTCTGATACAATGAC | 9886 |
rs764872401 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996659 | GCTTTTATCAATTTC[-/A]TTAAGCTTAACAACC | 9886 |
rs764879562 | snp | C/T | 1.68038e-05 | 0.00289855 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878070 | ACACCTGAAATGTTA[C/T]ACAAAAAGCTAAATT | 9886 |
rs764959747 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883003 | TTTTCTTGTTATCCC[C/T]ATTTTACAGATGAGG | 9886 |
rs764960166 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974992 | TGTATGTGTGGCTGA[A/G]AGCTGTATGATCTTA | 9886 |
rs764969898 | snp | A/C | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888390 | CACCAAATCCTTTTC[A/C]TTTTCATCCAGTTGT | 9886 |
rs764971665 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907382 | CCCTTTAAGAAGAGG[C/T]GCTTTCCTTGCCAAA | 9886 |
rs764990527 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899265 | CAACGAATGCAGGAG[A/G]CACTGAAGTAAAGAA | 9886 |
rs765022264 | snp | C/T | 8.27027e-05 | 0.00642997 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888484 | ACCACAGTCATGGGC[C/T]CCATCCGCTTTGAAA | 9886 |
rs765039976 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938062 | AAAAGCATCGAACAG[A/G]TCACTTAAGAAAGAC | 9886 |
rs765041776 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910945 | TATCCCAAAGCCTGA[C/G]AGAAACACTCACTTC | 9886 |
rs765071744 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871369 | GGAAGATCAGTGCCC[A/G]AAACCTGAACTATGT | 9886 |
rs765140879 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991045 | CTGTCAATTTTACCT[A/C]CTACATATCTCTTGA | 9886 |
rs765155637 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999871 | ATGCCATTTCATATA[C/T]AGCTTTTTGAAATGC | 9886 |
rs765172781 | snp | C/T | 1.67792e-05 | 0.00289643 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886267 | ACAACCATGAGCCAA[C/T]TTTGCTGAGAGCTTC | 9886 |
rs765183985 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979217 | TTATTTTCATCTGTA[G/T]CTACCTTTTTTTGCC | 9886 |
rs765212274 | snp | C/T | 3.30256e-05 | 0.00406346 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874986 | AAGAGAGCACTTCTC[C/T]GTCAATGCCCACGCC | 9886 |
rs765223333 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899667 | CATTTCTTGCAGAAA[C/T]AGTAATTGAGAACCT | 9886 |
rs765226841 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937334 | ATCAGTCAGCAACAC[A/G]TGACAAAAAGAAAAA | 9886 |
rs765245714 | in-del | -/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002580 | TAGAGATAGCTATTA[-/T]TTTTAGCAGAAATAA | 9886 |
rs765264452 | snp | C/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874733 | TAGGGGACAATGGGA[C/T]TGGCATGGGGGTGGG | 9886 |
rs765288622 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968205 | TGTGTCTCTGGAGAA[A/G]TGTAAATTATCTTTC | 9886 |
rs765294706 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966244 | CAAGTTTATCTGTCT[A/C]TATTTTTAGCTGTCT | 9886 |
rs765317595 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873863 | AGGATCTACCATTTA[A/T]ATGTACACGGCCTTT | 9886 |
rs765321767 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989025 | GGGATAATATTCAAT[A/G]CTCTAAAAATTATAG | 9886 |
rs765324320 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930061 | GCTCTATAATATGAA[C/G]AAAAAAATCTCAACC | 9886 |
rs765334826 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901522 | GTGTCCTTTATTGAT[A/G]TGGAATAGCTGAAAG | 9886 |
rs765420189 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982630 | ATCTCCAGTCATTAC[C/T]AAATGCCTCCTGATG | 9886 |
rs765463803 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60952089 | AAAAAAGAACGGTAC[A/G]TGATAAAACTTTTAT | 9886 |
rs765489430 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909055 | CGATGGAGTCACAGG[-/A]AAAGAGCAGCTTATT | 9886 |
rs765498528 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928858 | GTCTGTTCTCACATT[G/T]CTATAAAGAATTGAG | 9886 |
rs765567057 | in-del | -/CTC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977385 | GTATGGCTGCTTATG[-/CTC]CTCCATACAAGCAGC | 9886 |
rs765568144 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962327 | AGAGATACTTACCTA[C/T]AATAGATAATATATC | 9886 |
rs765596580 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913412 | TGGGTGGGGAAAAAG[A/T]GTCTTTAAAAATCTC | 9886 |
rs765604546 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884515 | CCAACAGTTTGTAAA[A/G]AGACAAAGAGGCTGT | 9886 |
rs765614061 | in-del | -/AC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950219 | CTAGAAAAGAAAAAG[-/AC]AACAATTTAATGTAT | 9886 |
rs765621276 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891859 | AATCCCCATGTGTCA[C/T]GGGAGGGACCTGGTG | 9886 |
rs765626836 | in-del | -/CTC | 1.66593e-05 | 0.00288607 | cds-indel, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60871472 | TTTTTTGTTTTTTTT[-/CTC]TTCCTCTTCAGGCCA | 9886 |
rs765675866 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898221 | TCACTGTGCATGAGT[C/G]CCCCTCTGGCAAAGA | 9886 |
rs765683584 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963392 | CCTGAAAGATAAATT[A/C]TCAGGTATTAGAAGA | 9886 |
rs765717418 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906236 | AGATTCCCATTCACT[C/T]TCAGAAGGTTTGCTT | 9886 |
rs765741169 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981966 | AGTTGAAATGGGTTT[C/G]CACCATGTTAGCCAG | 9886 |
rs765749631 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922760 | GAGGATGGACCAGGT[-/AG]AGAGAACAAAGTATG | 9886 |
rs765756036 | in-del | -/GGTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880138 | CTGAGTTGGGGGGGT[-/GGTT]GGTCCTGGAACCAGT | 9886 |
rs765779120 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994690 | ATATTTGAGTCTACT[A/C]TCTTTAAGGCACTGT | 9886 |
rs765801957 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878505 | ATGAGCAACCACCCT[A/G]GCTGCCACAGTGACC | 9886 |
rs765807377 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951474 | ACATGACCTAAATTT[A/G]TCATTTGGTAAACTC | 9886 |
rs765836916 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916967 | GAAGGGGCTGCAAGC[C/T]AGGTAATGTATGTGA | 9886 |
rs765837289 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879955 | GTACAGACTTTTTTC[C/T]TGTCATTATTCCCTA | 9886 |
rs765858818 | snp | A/G | 6.67212e-05 | 0.00577548 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911005 | CCTGCAGGAGAGAGA[A/G]AGAGCATCTGTGCTC | 9886 |
rs765876407 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878711 | TATGACTGGGTACAG[A/G]TGAACTGTCCCTTGT | 9886 |
rs765933781 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987404 | CCTTAAAATCAGTGG[C/T]ACTGCCACTCTCCCT | 9886 |
rs765944339 | snp | C/T | 1.89159e-05 | 0.00307532 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911336 | GGGATGCTGAAGACA[C/T]TCTGTGCATCTTACC | 9886 |
rs765951496 | snp | C/T | 1.70394e-05 | 0.0029188 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871454 | ATTACCGATTGGTTT[C/T]TGTTTTTTGTTTTTT | 9886 |
rs766008467 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934948 | ATGAGACATAGAGAG[G/T]AGGGGAAGATATAGA | 9886 |
rs766027459 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958215 | TAAGGTTGAAGCCTG[-/A]AAAAATTTAGTTTTG | 9886 |
rs766032122 | in-del | -/AC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900789 | ATAATGTGAGCCATT[-/AC]AGTTCTTCAGACTGT | 9886 |
rs766033462 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963617 | AGGTCATGTGTTCCA[C/T]TGGAACAGGAAAAAT | 9886 |
rs766042195 | snp | C/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977950 | GTTAACTGATATGCA[C/G/T]AGGAAAGAAATAGAT | 9886 |
rs766048603 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958040 | ATACAGACCCCACAG[C/T]TAATCTCATTAAAAA | 9886 |
rs766065263 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897161 | GGCCCTAGCTAGACT[C/T]TGAACAGCAAAATAC | 9886 |
rs766069785 | snp | C/T | 0.000247103 | 0.0111126 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888883 | TCGGCACATAGAGGA[C/T]TGTCCAGTAAACAGG | 9886 |
rs766105195 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916325 | GCCAATGGCTGTCAC[A/C]AAGTGCTGGATAATG | 9886 |
rs766111796 | snp | A/G | 1.65411e-05 | 0.00287581 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875050 | ATGCTGTTCTGGGGA[A/G]GAGAGAGGGGGCAGG | 9886 |
rs766121047 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899717 | TCTAGACATTGGGGA[C/T]AGAGTGATTAGTAAA | 9886 |
rs766175071 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900315 | ACTCTGCTGAGCCTG[C/G]GAGGGGTCCCCTACA | 9886 |
rs766201965 | snp | A/G | 3.36412e-05 | 0.00410115 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888585 | AGGAACTGCACCCTC[A/G]GCTTCCAGCCCCAGA | 9886 |
rs766207288 | in-del | -/GA | 0.000819898 | 0.0202306 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910996 | CTCCAAGACCTGCAG[-/GA]GAGAGAGAGAGAGCA | 9886 |
rs766212179 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938162 | ATTTTATCTCAGCAC[C/G]ACTGAAGATAAGTGA | 9886 |
rs766235305 | snp | G/T | | | nc-transcript-variant, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000927 | GCATGAGGAGCTGCA[G/T]ATGCTGCGCCTACTT | 9886 |
rs766293623 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999258 | GTGAAGGAAATGAAA[A/G]GAAAAGTCCACTAAA | 9886 |
rs766309683 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910368 | TTCATTTTGGAAATA[C/T]GTCTTGCGAAGGACT | 9886 |
rs766342377 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968392 | CCTAGTTCAATGTTT[C/T]AAAACAGGAGTATGA | 9886 |
rs766363001 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876654 | AGCCTCCCAGAGTGA[A/G]TATTTTAAAAAACTA | 9886 |
rs766395366 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969661 | AGAGAGTCCTATTGT[C/T]TGTGTGTTTTAGCAT | 9886 |
rs766436195 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880789 | AATTATTCAACTAAA[G/T]CTAGCACCAGTTACA | 9886 |
rs766451950 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919888 | TCTACCTTATGTGCT[A/G]TTCTTAATAAACATT | 9886 |
rs766473768 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918722 | CACTATGTCTCTTGT[A/T]ATATTTGCATTTCTT | 9886 |
rs766487457 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973407 | TCGTCTTCTTTAAAA[C/T]TTTTAGCATAAACTG | 9886 |
rs766490053 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966812 | CATTTACATTAGGTA[C/T]ATCTCCTAATGCTAT | 9886 |
rs766494205 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958675 | GAGGCATGATCACAG[C/T]TCACTGCCTTGACTG | 9886 |
rs766551868 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912024 | CAATATCTGTTGTTG[A/T]AAAGCAGTTTTCTAT | 9886 |
rs766558230 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960635 | CTTGGATCATGTCCC[C/T]ACCATACATCTGATG | 9886 |
rs766595518 | snp | C/T | 0.000362408 | 0.0134563 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888937 | GGACACTCTGGAATT[C/T]TGATGACCGGTGGAG | 9886 |
rs766606811 | snp | C/T | 1.65312e-05 | 0.00287495 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888261 | CCGATTGGCTTTCCT[C/T]ACGTGAAAGGCTTTC | 9886 |
rs766619241 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942623 | TGCAGACATTATTTA[C/T]GCTGAAAAGAGCTTG | 9886 |
rs766706671 | snp | C/G | 1.6966e-05 | 0.00291251 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878088 | AAAAAGCTAAATTCT[C/G]CTGCAGAAAGCAGGG | 9886 |
rs766728509 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901656 | TTCTTCATCAGAAAG[G/T]TCCAGTATAAACACA | 9886 |
rs766739313 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874066 | CTCCTCTCCCTGAAA[C/T]CACCTCCTTTCCTTT | 9886 |
rs766755283 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982866 | CATGTGAATTTCATG[G/T]GCGTTTCATTTGCCC | 9886 |
rs766762096 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881516 | GAAAACAATGCCTCT[C/T]GTGATAGCGCAAGAG | 9886 |
rs766793678 | snp | C/T | 1.65157e-05 | 0.0028736 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886109 | TTTTAGGAAGGCACG[C/T]ACCTCACTGTTGGCA | 9886 |
rs766805473 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913037 | GTAAAGCCTAATACA[C/T]AATTGGGACTCAAGT | 9886 |
rs766821423 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870956 | CCAATTTGCACTTTG[A/G]GAGATTTCAGTCCCC | 9886 |
rs766835283 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951551 | AGCCATTAAACACTT[A/C]AGGGTCAGCATCGAA | 9886 |
rs766860154 | snp | C/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874877 | TCATTTAGACAGATG[C/T]AACAATGGAATGTTT | 9886 |
rs766875553 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898089 | TGTTCCATGGTAGGA[G/T]CCCACCTCTTTATAT | 9886 |
rs766875796 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885384 | TCTTCTCTAAGCATA[C/T]GTCTCTTCTAGAGAT | 9886 |
rs766897302 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869784 | AGCCTATTGAAAATA[A/G]TTAAGATGGATGCAT | 9886 |
rs766902370 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994967 | ACATAATGAAAGATG[A/C]GGCTAAAAATTCTTT | 9886 |
rs766915372 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898174 | ATATGGACAGACATT[C/G]TGGTCACATTTTAAT | 9886 |
rs766925176 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983547 | TTTTCCTCTTGGATA[C/G]TTTACTCTTTATTGA | 9886 |
rs766970720 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906729 | GTTGTTATCACTGTC[A/G]GCAACATAGGCTTTA | 9886 |
rs766996774 | snp | C/T | 1.68267e-05 | 0.00290053 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888590 | CTGCACCCTCGGCTT[C/T]CAGCCCCAGAGCCTC | 9886 |
rs767074971 | snp | C/T | 1.66355e-05 | 0.002884 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888685 | CTTTCTTCCTCTGGG[C/T]CGACACTCAATATCC | 9886 |
rs767081009 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923747 | CTCCATACTGTTCTC[A/G]GGATAGTGACTAAGT | 9886 |
rs767115133 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871580 | GTTCCCTTTTCACAC[A/G]CTGGTAGTGATCTTC | 9886 |
rs767147300 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940344 | TTACAAATTACTCTA[C/T]GAAAAGAAAGAGGGG | 9886 |
rs767153209 | snp | A/G | 1.65507e-05 | 0.00287664 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875061 | GGGAAGAGAGAGGGG[A/G]CAGGAGAACATTAAA | 9886 |
rs767201042 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996526 | AGATGACCTGATGTC[C/T]CCCACTGTAGATGAC | 9886 |
rs767287275 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957306 | ATACTTTTATATGAC[C/T]GTCAGCTTTGTACAT | 9886 |
rs767347209 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928628 | GCAGAGGCTGGAAAG[G/T]GTAGTGGAAAGGGGA | 9886 |
rs767353308 | snp | A/T | 1.67899e-05 | 0.00289736 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877898 | CATGGCCCTGAGTCA[A/T]CATCCTTACCTGCAA | 9886 |
rs767388009 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918469 | GGAGTTCTGCCCCCA[C/T]AACTCAATAACTCAG | 9886 |
rs767416067 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964163 | AATATAACGCATGCA[A/G]CGTTATTTTCTAATA | 9886 |
rs767432117 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906384 | AGAGCTCGTAATAGA[G/T]GGTGAGTGCTGGTCT | 9886 |
rs767457791 | in-del | -/GGC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960330 | CCTATTGATTATGCT[-/GGC]GAATTTAATCAAATA | 9886 |
rs767548740 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880065 | GAGGATGTGCACAGA[C/T]CTATGCAAATACGAT | 9886 |
rs767556521 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60892949 | TTTTCACATGATTTA[A/G]GGAATTGGGATTAGC | 9886 |
rs767592095 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991249 | AACTACAGCACTCCC[C/G]ACACCCCCACCAAAA | 9886 |
rs767627608 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938568 | AAAATACATTTAAAA[G/T]GACCTAAGCAGTTAG | 9886 |
rs767649469 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962022 | CATGTTGGCCAGGCT[G/T]GTCTCAAACTCCTGA | 9886 |
rs767656559 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987351 | CTTTTTGGATGCTTC[A/C]TCCCCATCCTCTCCT | 9886 |
rs767683646 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932453 | CAAAAAGTCATCAAG[A/C]TGTACATTTGCGATC | 9886 |
rs767686808 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937481 | AATATTTCTTAGTTA[G/T]CTGGCTGGAAATAGT | 9886 |
rs767704200 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961032 | GTACTCAGAGAGTCA[A/G]CTGTGCTTTACCCAG | 9886 |
rs767726418 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923995 | TGAAGAACTGAGGAG[C/T]GGAGTGTGATTTAAT | 9886 |
rs767746470 | in-del | -/G | 1.72335e-05 | 0.00293538 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893022 | TCATAAAAGAAGCTT[-/G]TATTGCCTTTTAACA | 9886 |
rs767748889 | in-del | -/CT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895515 | GTTCAAGCAATTCCC[-/CT]GATTCAGCCTCCTGA | 9886 |
rs767758396 | snp | G/T | 6.59055e-05 | 0.00574007 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872276 | CCAGGCGGCCAACTG[G/T]TGGGCATTGTGAAAC | 9886 |
rs767791523 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60909069 | GGAAAGAGCAGCTTA[A/T]TTTTGTTGGGAGGGA | 9886 |
rs767803910 | in-del | -/A/AAAAGGTA | 4.97618e-05 | 0.00498787 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874925 | TGATTGAACACACTT[-/A/AAAAGGTA]AAAAGGTAAAAAGCA | 9886 |
rs767856544 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902888 | CGTTCAACTAACATC[A/G]ATCAAGCTCCTACAA | 9886 |
rs767864173 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931271 | GTGCAACCATTCCTG[C/T]GATCTAATTCCAGAA | 9886 |
rs767881157 | in-del | -/TGAG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933847 | CACTCATTGTTATAT[-/TGAG]ATGTTCATGAACAAT | 9886 |
rs767912059 | snp | A/C | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889088 | CATCCTTGATACCAA[A/C]CTGGTCAAACACGCT | 9886 |
rs767915487 | snp | C/T | 4.99621e-05 | 0.00499786 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60871472 | TTTTTTGTTTTTTTT[C/T]TCTTCCTCTTCAGGC | 9886 |
rs767915644 | snp | A/C | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942786 | CTAAGACCAAACAAA[A/C]ACAGCCTATTGACTA | 9886 |
rs767943200 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876018 | TCTGCATGCTTATTG[G/T]TCAGTATGCCTATAT | 9886 |
rs767965913 | snp | A/C | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913278 | GCAGGAATGGAGTAG[A/C]GTGATTCAAGGAACA | 9886 |
rs767966043 | snp | G/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886118 | GGCACGTACCTCACT[G/T]TTGGCACTTTCCACA | 9886 |
rs768008265 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886982 | CATACTATGATTACA[C/T]CTAAGAAAATTAAAA | 9886 |
rs768027183 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944681 | CTTTCTTCCCCCTAG[C/G]AGCTGACCGGCCGCG | 9886 |
rs768028780 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991069 | CTCTTGAATCCATTC[A/G]CCTTTTGGAAGTCAC | 9886 |
rs768104702 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972554 | ATGGGGGGCTAGAAG[A/G]GGGATAGCATTAGGA | 9886 |
rs768122587 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899496 | TGGGATTAACCTCCC[C/T]GACTCTTCTGAGACC | 9886 |
rs768149895 | snp | G/T | | | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872131 | ACATAGAAGATAAAA[G/T]CTTCCATGAGAGGTG | 9886 |
rs768192876 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891075 | AGTCTCTCATTTACT[A/G]TGGACTTCTTAACCT | 9886 |
rs768199313 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-3-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945150 | GAAAGCAAACAACCG[A/G]GTGCCTGCCATCAGG | 9886 |
rs768199658 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998935 | ATAAACTGCTCATCC[C/T]TGGGCATGAAAGCTT | 9886 |
rs768205318 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937930 | AGGATTTTATAACAT[A/C]CTCATAACCCTCTGA | 9886 |
rs768208952 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969831 | AGGCTATGCTTTTAG[A/T]ATTTAAAGAAATAGA | 9886 |
rs768212439 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872229 | AACTTGGAGCATACA[C/T]TGTTGTAGTTGGTGC | 9886 |
rs768226167 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969228 | AAACCTAAACCCAAC[G/T]GTGCAGATACAGGGT | 9886 |
rs768238326 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873267 | AGAGAACCAATTGTG[G/T]GCATTTCTTCCCTAC | 9886 |
rs768260451 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950255 | TGTATCTTTGACATT[C/T]TAAAAAGCAAAAATA | 9886 |
rs768295520 | snp | A/C | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886148 | AAATGACCCCCCGAA[A/C]ATGGCTGCCATCCAC | 9886 |
rs768351932 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980209 | GAATATGAGCAAGAC[A/C]TTAATGATAGGTGAT | 9886 |
rs768351995 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992623 | TCTCAATAAATAGGC[A/G]AAACTCAAATGTTGC | 9886 |
rs768358227 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922362 | CAATGAAGGCACTGA[A/T]GCCTTGAACCCTCCT | 9886 |
rs768362041 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927467 | GACTTCAAATCATAC[C/T]ACAAAGCTATAGTAA | 9886 |
rs768377784 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941341 | GGTTTCACCTCCCAG[-/A]GATTTTTTTTTTCTT | 9886 |
rs768380813 | in-del | -/TTG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961826 | TTTTTTTTTTTTTTT[-/TTG]GAGACAGAGTTTCCC | 9886 |
rs768417070 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888900 | GTCCAGTAAACAGGC[A/G]GCTTCATTTGTCCCC | 9886 |
rs768436974 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949486 | TTACTCAGACCAACT[C/T]TTCAGATCTCTAAAG | 9886 |
rs768445947 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924434 | ATTATATAATGACAA[-/G]AGGGGTCAATTAAGC | 9886 |
rs768461175 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910910 | TGCAAAGCGTCTGTC[C/T]TTGTGATGATCACCA | 9886 |
rs768509562 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903422 | CACTCAACTCGGCAC[C/G]CAATTTCTAGTCAGA | 9886 |
rs768527257 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894256 | CTGTGTCTTTAAATT[C/T]ATATCCAAGAAAAGC | 9886 |
rs768530657 | in-del | -/ATT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985328 | TTTTTTCAAAAGCTG[-/ATT]TTACTCACTTGGGAT | 9886 |
rs768539896 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992306 | GATGTAACTGGTTTT[A/C]TGATATAAGATGTGT | 9886 |
rs768540161 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961785 | TGCAATGCTATTAAT[A/G]CAGTGGTGATTTATA | 9886 |
rs768540298 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930882 | TCCATTATTCCCTCC[G/T]ACAAATAAACGAATC | 9886 |
rs768540527 | snp | A/G | 3.31879e-05 | 0.00407343 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886090 | CATAAAGACACCACT[A/G]TGCTTTTAGGAAGGC | 9886 |
rs768568629 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974277 | TTCAATTGACAAAAC[A/G]TAATAATGGAAACTG | 9886 |
rs768600511 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923120 | TTGGAATATACTTCA[A/G]TCCTTGGCCTTTGTG | 9886 |
rs768619047 | snp | C/T | 1.64732e-05 | 0.0028699 | stop-gained, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889017 | CTTTAGGTGGGATTT[C/T]CAGAATTGCAGGTGC | 9886 |
rs768628826 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906548 | ATTCAAGAGGAAAGT[C/T]CAGCTGCACTCTGTC | 9886 |
rs768671236 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913154 | AGAAGAATTCTTTTT[C/T]ACAGTTAGGACTATT | 9886 |
rs768687611 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968663 | CAAAACCTACATATA[A/C]GTAAGCCTCAAATAA | 9886 |
rs768698225 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911694 | GAATGTTTGGAAGTT[C/T]GTACTAAGCCTAATT | 9886 |
rs768699568 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870148 | TCTCTGTGTGTGTAT[A/G]TGTGTGCTGTAACAT | 9886 |
rs768706822 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883630 | GTCAGTCAAATACCA[A/G]CTGGATGAGGTTTTA | 9886 |
rs768729388 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990977 | ACATGTTCCTCCACC[A/G]TTGTTCCCTGACACT | 9886 |
rs768740594 | snp | C/G | 1.66452e-05 | 0.00288484 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875094 | ACGCCCTGCGAGCCA[C/G]GTAGCTTGCCTGGAG | 9886 |
rs768760190 | snp | A/G/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882856 | AATACCCTTAACCCC[A/G/T]TATGGAAAGAATTTA | 9886 |
rs768772092 | snp | A/G | 3.29935e-05 | 0.00406149 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877967 | GCAATTAATTCCAGC[A/G]GGTCCAGATCCAAGT | 9886 |
rs768772830 | snp | C/G/T | 8.37326e-05 | 0.00646997 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888657 | CTGAGGAATCCTAGG[C/G/T]GGGCCCTCCTCCCTT | 9886 |
rs768854645 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874462 | GAAGCTAAAGCTGAA[C/T]CTTGGACCTTCTCTG | 9886 |
rs768861255 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924561 | GCCAGGGACTTCAGT[A/G]TCCCACCTTCAGCAT | 9886 |
rs768865768 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878498 | AGAGAGGATGAGCAA[C/G]CACCCTAGCTGCCAC | 9886 |
rs768873474 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979327 | CCAATAGGAAAAATA[A/G]TAAGGAAAGGAATAT | 9886 |
rs768881376 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995771 | ATGCAATTTCAACTT[G/T]GAAAAGGGAGATTTT | 9886 |
rs768921533 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963237 | ACAGAGACCCAAATG[G/T]CTCAGCAAGTATTGA | 9886 |
rs768953750 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892888 | CACCCAACAAGGATA[A/G]CGGGTGTTCGAGGGC | 9886 |
rs768956980 | snp | A/G | 1.69709e-05 | 0.00291293 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888215 | CGGCCCACTCACCCG[A/G]GAACGTTCCCTTGCT | 9886 |
rs768958443 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965247 | AAATGCTTAGGTTTT[A/T]TATATATTATATACT | 9886 |
rs769014428 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890738 | AATTTGGATTTGACG[A/C]CTTAGATGAAAAGGA | 9886 |
rs769053685 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963171 | GCAGGAATGTTCTCA[A/G]AGCCACTCATTGCTG | 9886 |
rs769109067 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965700 | GGCAATTCTTCAGGA[-/T]TTTTCCATTACCTTA | 9886 |
rs769124867 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000433 | AGAGCAAGATGATGC[A/G]ACAGGATTCTCAGCA | 9886 |
rs769137600 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889038 | TTGCAGGTGCCTGCG[A/G]GAAATCAGCGCTGCT | 9886 |
rs769153366 | snp | A/C | 6.59337e-05 | 0.0057413 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888323 | TCATGATGTTTTCCA[A/C]CATCATCCTCAAATC | 9886 |
rs769178200 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987095 | TGTGCCACAGGGAAA[A/G]GAAGAGAAAGAGAAA | 9886 |
rs769184320 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989978 | AACCTCAGAATGTCC[-/T]TTTTTTTTTTTTTTT | 9886 |
rs769186442 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965541 | CAATACATATTTGTA[-/AG]AGAATTAATTGGTGT | 9886 |
rs769199023 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900228 | ACTGGGAGGGTCAGC[A/G]GATAGGGAGGGAAAG | 9886 |
rs769201548 | snp | A/C | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60882962 | TACACATGTCCTCTC[A/C]TGCCTTCTCTGCCCT | 9886 |
rs769210807 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957764 | TGGTAATGATATTTA[C/T]TGAATGCTCACTCCA | 9886 |
rs769211426 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918390 | TCCCTCTCTTATGAA[-/AG]AGACTCCCAGGAAGT | 9886 |
rs769219103 | in-del | -/A | 1.75875e-05 | 0.00296538 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889195 | ATGGGCCTGAAATAG[-/A]ACATTTTAAAAATTA | 9886 |
rs769251082 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889871 | TTTGTCGACAGTAAG[C/T]GCCTGATAAATGTTA | 9886 |
rs769264509 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929603 | CTACATAGTTATTTT[A/G]AATTTAGTTACAAAA | 9886 |
rs769281777 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940345 | TACAAATTACTCTAC[A/G]AAAAGAAAGAGGGGA | 9886 |
rs769291250 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957839 | CCATTCCCACTGTAC[A/G]GACAGGAAAGCTGAG | 9886 |
rs769294088 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949245 | TCTCAAACAAGATGA[C/T]GTCCAGCCTTCCATC | 9886 |
rs769313889 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975612 | ATGGAGTTTCAGTAA[C/T]ATTCTCCACGTGCTG | 9886 |
rs769351017 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917979 | AAAAACAAATGTACA[C/T]GCATCCATACACACA | 9886 |
rs769370111 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911275 | AATTTATCCACGCTC[C/T]TCCTTTAGAAAAAAT | 9886 |
rs769386668 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939025 | TGAGATCATAACCTC[A/C]TTAACGCTGGGAACT | 9886 |
rs769400402 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000889 | AACCAAGAAAAATCA[A/G]TCCCGCATCACCTTA | 9886 |
rs769429843 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903758 | CCAGCATGATTTTGT[A/G]TGACAGTATGACAGT | 9886 |
rs769477152 | in-del | -/GG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994611 | GATTTTCTAATGTGA[-/GG]GAAAGATATCCTCAG | 9886 |
rs769496595 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60891043 | ATTTTTATACAGAAA[A/G]TTGCTGAGGCCAGGA | 9886 |
rs769513142 | snp | C/T | 1.99651e-05 | 0.00315945 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911328 | GTGCCCTAGGGATGC[C/T]GAAGACACTCTGTGC | 9886 |
rs769528890 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986054 | CATGAGAATGAGAAG[A/T]ATGCCAGCCAACTAC | 9886 |
rs769555908 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970475 | CCATATAATTCAGAT[C/T]GGTATTGAATATTAA | 9886 |
rs769573997 | snp | C/G | 3.29614e-05 | 0.00405951 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886165 | TGGCTGCCATCCACT[C/G]ACAGCTACAGATCAG | 9886 |
rs769590131 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992799 | TGATTTTGATCTAAC[A/G]CAAAGGGGAAAAAAA | 9886 |
rs769612708 | snp | A/C/T | 3.36317e-05 | 0.0041006 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888581 | TCTCAGGAACTGCAC[A/C/T]CTCGGCTTCCAGCCC | 9886 |
rs769648366 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895624 | GGTCAGGCTGGTCTC[A/G]AACTCCCCACCTCGG | 9886 |
rs769667262 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971168 | ATTTTTTCACTTTGT[A/G]TTTGTAGAAATTATT | 9886 |
rs769671725 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884859 | GGGGAAAGGAAAGCC[A/G]TCTGTCAAATATACA | 9886 |
rs769684346 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871546 | CGATGCTTATTTAGT[A/G]CAATATCTTCCTTCT | 9886 |
rs769702178 | in-del | -/TTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949667 | TTCCAGGTGAAGCTT[-/TTT]TTTTTTTTTTTTTTT | 9886 |
rs769728034 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950613 | CCGCAAAGTTCCATA[A/T]GTCAAATGGGGACAA | 9886 |
rs769737516 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912760 | CCAGGGACAGGACCC[C/T]CCACAAACAGGGGTG | 9886 |
rs769771403 | snp | C/T | 1.65537e-05 | 0.0028769 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886223 | ATCGTCCAATTTAAA[C/T]GTCACGTCTGCCAAG | 9886 |
rs769800796 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894784 | CCTAAATGTGTTATA[A/G]TATGTATAAAATAGT | 9886 |
rs769823397 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965530 | TAGTAGGTGTTCAAT[A/G]CATATTTGTAAGAGA | 9886 |
rs769826444 | in-del | -/GAA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000345 | ACACACTGAAACACT[-/GAA]AGTAATAAAAAATAT | 9886 |
rs769839144 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873409 | AAACACTTACCAGCA[C/T]ATCACTAGGTTAGGG | 9886 |
rs769844316 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925416 | ACATTCCAAAACCTA[C/T]GGAACACTGCACAAA | 9886 |
rs769875758 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981257 | AACTCCAAGGCAATG[C/T]GAGGTCCCCAGAATT | 9886 |
rs769880661 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983419 | ATAGTTATAGTATAA[G/T]CCCATGTTAAGATGA | 9886 |
rs769895710 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924588 | GCATTGGAAAGATCA[C/T]CTAGACAGAAAACCA | 9886 |
rs769917294 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60885952 | CCCTCAAGCACTACT[A/C]AGGAGCAATAGCTCC | 9886 |
rs769920099 | snp | C/T | 4.94768e-05 | 0.00497352 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877993 | CAAGTTAGGAGACAA[C/T]TGCTTGGTATAGAGA | 9886 |
rs769928956 | snp | G/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892891 | CCAACAAGGATAACG[G/T]GTGTTCGAGGGCAAA | 9886 |
rs770010501 | snp | C/T | | | intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60898677 | TTAATACTTTACCAA[C/T]AGCGTGAGGCTTCTT | 9886 |
rs770016280 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872251 | AGTTGGTGCAGATGT[A/G]GTGCAAACACCAGGC | 9886 |
rs770040065 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875851 | CCATCTCTTGCCTTT[C/G]TAAGGGCTGTCACCT | 9886 |
rs770041661 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876739 | AATCTAATATTGATG[C/G]CTCAACTCGCTCTTT | 9886 |
rs770051521 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918609 | ATTAAGATGAGTGGG[C/T]AGGAAGAGAGTTATC | 9886 |
rs770076773 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984573 | CTTCTTCAAATAAGC[A/T]ATTACTTTGGGGACT | 9886 |
rs770095224 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954883 | CAAGTTTCGGAAATA[C/G]TTCATATTTTATCCT | 9886 |
rs770106523 | snp | C/T | 3.2963e-05 | 0.00405961 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888347 | TCAAATCGAACATCT[C/T]GAGGACCTCTGCGAT | 9886 |
rs770119336 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913806 | CCCCCATTTTCCAGT[A/C]ATTGGACTTTGGGCA | 9886 |
rs770128049 | snp | C/T | 1.73297e-05 | 0.00294356 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893023 | CATAAAAGAAGCTTG[C/T]ATTGCCTTTTAACAG | 9886 |
rs770128578 | in-del | -/G | 1.64933e-05 | 0.00287165 | frameshift-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888449 | GAAAAGGGCCTGGCT[-/G]GACTGAAGCGTCCAT | 9886 |
rs770152965 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879493 | CAGTGCCACCACGCC[C/T]GGCTAATTTATTTTA | 9886 |
rs770156188 | snp | C/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888429 | AAGAAACTGGAGCAG[C/G]GTCCGAAAAGGGCCT | 9886 |
rs770164723 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911614 | AGAGCAATCAAAGAC[C/G]TAAGAGGTTCAGGGA | 9886 |
rs770187275 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935027 | TTGTTTTGCATACTG[C/T]TATCTGTACAAGAAT | 9886 |
rs770212274 | snp | A/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988308 | ATTTTTTAAAAAATA[A/G/T]AATTTCTACTTTTAT | 9886 |
rs770233493 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978529 | TATGTTGGGTCTCTG[C/T]GTATTGTATCAAAAC | 9886 |
rs770265653 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989379 | AAGTATATTTTATGG[C/T]AGATTTTCCATGAGG | 9886 |
rs770303992 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918265 | AAAATAGGGACAGAG[A/C]CAAATGTGACCTTAG | 9886 |
rs770335949 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60870930 | TCAACAGAACAAAGA[C/T]TAAACACTCTCCAAT | 9886 |
rs770348507 | snp | G/T | 0.000332253 | 0.0128847 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874911 | CAGCATTAAATGAAC[G/T]GATTGAACACACTTA | 9886 |
rs770379024 | snp | A/G | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869338 | CTGGAGCATGCACAA[A/G]CCCCCATGACCCAGC | 9886 |
rs770398947 | snp | C/G | 1.6945e-05 | 0.00291071 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889176 | CAAAATATCCCCTCT[C/G]TTTATGGGCCTGAAA | 9886 |
rs770413845 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971794 | TTTTGCAATCTATCC[A/G]TCTGACAAACTGCTA | 9886 |
rs770434487 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892656 | TAGAAGGGCTCAGGG[C/T]ACACTCCTCATGATT | 9886 |
rs770462782 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918335 | GTGGTACCCCAACCC[A/C]ACCTTCAGTCTTTGC | 9886 |
rs770468059 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929719 | CCAAAAAGCATATAA[C/T]AAAATGAAGAAAACT | 9886 |
rs770470856 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906120 | ACTAGATAATAAATG[G/T]GTTCTAACTGGACTC | 9886 |
rs770479842 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906987 | GCAGGTCTTTCTCAT[G/T]CTATTCTCATGACAG | 9886 |
rs770491587 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60902110 | GCTCTTCTGTTTTTC[C/T]CTTCTGGGTAGAATA | 9886 |
rs770519329 | snp | C/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883183 | GTCTTCAGTGGCTTG[C/G]TTCCGTGGTCTTTGT | 9886 |
rs770530151 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002463 | GGTGTAAAACTTTAT[A/G]GGAGAGGCAGTCTGC | 9886 |
rs770539269 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988404 | GGTACAAATTTTCCT[C/G]TTACCCAGGTAGTGA | 9886 |
rs770557772 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869689 | CTCATTGAAAACTCA[A/T]CTTCTACCATTTTAT | 9886 |
rs770558780 | in-del | -/TAAT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880769 | GTATGTACATATGAA[-/TAAT]TAATTATTCAACTAA | 9886 |
rs770566236 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60882183 | TCTATCCTACCTGCT[A/G]GATATAGTTTCTTTT | 9886 |
rs770567449 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988269 | ACACAGTTATATTTA[G/T]TTATTTCAAAGAACT | 9886 |
rs770619449 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880903 | TACAAATTTGTTTCT[G/T]TGTGTAGGAACATGT | 9886 |
rs770655283 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963709 | TGTGTTATGTTGCTA[C/T]TAAAATTCACAAGTT | 9886 |
rs770661815 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960049 | GGAGATTGGTAGGTG[G/T]TGTAGAAAGCTTTGA | 9886 |
rs770664391 | snp | A/G | 1.6701e-05 | 0.00288968 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888660 | AGGAATCCTAGGCGG[A/G]CCCTCCTCCCTTTCT | 9886 |
rs770685305 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964138 | GATTTTTCTTTTCCA[C/T]CTTTGTAAAAATATA | 9886 |
rs770718416 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873620 | TCTGGATCATTACAT[G/T]TTTCTCTAGGAGGAA | 9886 |
rs770748437 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982420 | GAGGGTGTATTGTGT[A/G]TCAGGCATTGTGCTC | 9886 |
rs770765414 | snp | G/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885108 | TTGTGGTGTTCTATT[G/T]CACAGTATGGTGACT | 9886 |
rs770774755 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994487 | GGCTTGTGAAAATGA[C/T]AGCACTTCCAGAAAA | 9886 |
rs770775112 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951878 | CCTGGTCAACATGAT[A/G]AAACCCCGTCTCTAC | 9886 |
rs770802511 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970766 | TGTCACAATACAAAT[-/A]AGGGCTTTTACAGTG | 9886 |
rs770803425 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940568 | CAAATTATGCTTTCT[C/T]AAAGATGCTGTGCAG | 9886 |
rs770808106 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911460 | GCACAGATCAAGCGC[A/G]TCTTCCCCACGGCAT | 9886 |
rs770812218 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951366 | GCAAAGATGACCTCA[C/T]TTCTTGCGCCTGACT | 9886 |
rs770822257 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874273 | AATTCTGCAGATGTG[C/T]CTGGCATTGTAAGAG | 9886 |
rs770860544 | snp | A/T | 1.65784e-05 | 0.00287905 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888729 | TCTGCTCTGCTTCTC[A/T]TTCTCACAGGCTCCT | 9886 |
rs770878356 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922887 | GGGTTAATCCAAGAA[G/T]GAGTCAGGTGAGGGG | 9886 |
rs770889508 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877706 | CCTAACAGGGCCCAC[C/T]ACAGAGTGGGTGCTT | 9886 |
rs770897899 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935342 | TAGTGGCTGGATAGG[G/T]GCATGAGAAGGGCTT | 9886 |
rs770901065 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926730 | GGAAGGAACATATCT[C/T]AACACAATAAAAGCA | 9886 |
rs770912029 | snp | C/G | | | upstream-variant-2KB, intron-variant, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944426 | GACACGGGTGGCAAA[C/G]GTTCCTCGGCTCTAC | 9886 |
rs770920970 | snp | A/G | 2.0926e-05 | 0.00323459 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871684 | CAGACCATAAGACCT[A/G]CGGTTCATTGATGCC | 9886 |
rs770963951 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956662 | TTTTACTTTTTAGAC[-/T]TTTTTTTTTTTGTTA | 9886 |
rs770970340 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904673 | AGGACCATCTGCCTC[-/AG]AGTCTTCTAGGTACT | 9886 |
rs770978796 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903508 | TCACCAGTTCCAGAA[C/T]GAACCAGCTACAAAA | 9886 |
rs771000895 | snp | C/T | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869181 | CCCCAACCCGCTCTC[C/T]GGCCCCAGGCAGTAC | 9886 |
rs771030240 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913870 | ATCTGTTAAGTGGGT[A/G]TCATAAAAATACTCA | 9886 |
rs771140170 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887993 | ACCTAACCTCTCTGT[C/T]CCTTGGTTTCTCCAC | 9886 |
rs771182700 | snp | A/C | 3.52199e-05 | 0.00419628 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893035 | TTGTATTGCCTTTTA[A/C]CAGGTTTTTTCTTTT | 9886 |
rs771202814 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915289 | CCATCTGGATAATGA[C/T]TGTCTGGTTTCTGAT | 9886 |
rs771210093 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904732 | CAGAACTCTTACATC[C/T]GAATGACTGCTCTGT | 9886 |
rs771214890 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974400 | TTCTCTTTGTTTTTC[A/G]AATTTCAAGATAAGG | 9886 |
rs771216281 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978940 | TTCTTCTATGATATG[A/G]TAAATGGCTGGCTGG | 9886 |
rs771218001 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60870687 | ACTAATGGTATCTTA[C/T]GTATTCAGGTCCACC | 9886 |
rs771222805 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907144 | CCTCCCCAGCCACAC[A/G]GAACTGTGAGTCCAT | 9886 |
rs771241308 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936080 | AGTACATTTGAAAAA[C/T]ATTCTTTCAGTATTA | 9886 |
rs771261769 | snp | G/T | 1.65782e-05 | 0.00287904 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874930 | TGAACACACTTAAAA[G/T]GTAAAAAGCAAACTG | 9886 |
rs771302114 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980466 | GTCTGGGTTGTGGAA[C/T]TAAACAATTGTCTAT | 9886 |
rs771369918 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903087 | GAGAGACACCTCACC[A/T]GGATTCCGAAGGTGA | 9886 |
rs771389886 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982779 | ATGCCTTTCTCACAC[A/G]TAGTAAGTTACAGGG | 9886 |
rs771389915 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967202 | AGGGAATAGCAAGTA[A/C]AAAGGAAAATTCTCA | 9886 |
rs771410384 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979981 | TATAGTAGAATGGGA[A/G]AGGGAGGAACCGGAA | 9886 |
rs771429714 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953599 | TATTGAAAGAAATCT[A/G]TCACACCTGTTGTTT | 9886 |
rs771466394 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889048 | CTGCGGGAAATCAGC[A/G]CTGCTCGGATTGCAT | 9886 |
rs771483560 | snp | A/T | 3.34521e-05 | 0.00408961 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888549 | GAACCCCTTACTCCA[A/T]CCGGTCAAAGTCTGT | 9886 |
rs771486370 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881175 | TGCTGCCATGTAAGA[C/T]GTGCCTTTTGTCTTC | 9886 |
rs771535041 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883493 | TGCGTTCCTGACCTC[A/G]ATCAACTTCTCCCTA | 9886 |
rs771541311 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910608 | GCAATCAAAGCAGCC[C/T]GCAGTTGGAGGGTGT | 9886 |
rs771580402 | in-del | -/AC | 1.66269e-05 | 0.00288326 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886082 | CATACATTCATAAAG[-/AC]ACCACTATGCTTTTA | 9886 |
rs771602496 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967285 | TTTCTTTGTTTGCCT[-/G]TTTTTTTTTTTTTTT | 9886 |
rs771626584 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886900 | TTTTTTTACAGATAG[C/T]ATGGCACTTCACTCC | 9886 |
rs771631249 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886663 | CATTTATAATATGCT[C/T]TACTCGTATGCTATA | 9886 |
rs771638727 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911481 | CCCACGGCATTGTCA[A/C]CCACGACCACACATT | 9886 |
rs771640117 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931695 | ACATAAATTGTTTTT[A/T]CAAAACTATATGTAT | 9886 |
rs771650138 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980122 | GACTATAGGAGGCAA[C/G]GGTGGAAGCAAAGTG | 9886 |
rs771688406 | in-del | -/TTG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984057 | CTCTAACTTTCTGAA[-/TTG]TTGTACTCTGTTCCT | 9886 |
rs771729942 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978987 | GCCAAATCTCCCCCT[A/G]TGTATCATGTGTCAC | 9886 |
rs771756203 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941992 | TACTTTTGCTAAGTG[C/T]CAGTGTTAATGTGGC | 9886 |
rs771764878 | in-del | -/T | 1.69807e-05 | 0.00291377 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871457 | ACCGATTGGTTTCTG[-/T]TTTTTGTTTTTTTTC | 9886 |
rs771766765 | snp | A/C/T | 6.59037e-05 | 0.00574004 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872211 | GATTTGATTTCCTTA[A/C/T]GGAACTTGGAGCATA | 9886 |
rs771782212 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908403 | ATGCCTCAAAGTTTA[C/T]GTCTTGAGTACATCC | 9886 |
rs771800250 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937008 | ACTAAAAGTGAAATT[A/G]CACCACCAGGATAAT | 9886 |
rs771800287 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950235 | CAACAATTTAATGTA[C/T]AATGTGTATCTTTGA | 9886 |
rs771830512 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920099 | TTGCCTATGTCATTA[-/C]TTCTGCACAAAGGCC | 9886 |
rs771834807 | snp | C/G | 1.6766e-05 | 0.00289529 | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911592 | AGTAAGGACACCAAG[C/G]CTTTCCAGAGCAATC | 9886 |
rs771847530 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929959 | ACCACATACTGGGCC[A/G]TAAGGCCCCAAATCC | 9886 |
rs771864912 | snp | C/T | 9.90818e-05 | 0.00703783 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878028 | CCAATACTGCTTGCA[C/T]TGATATCTTGTTTAT | 9886 |
rs771868785 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959006 | AGTGAGCCCTGCCTC[C/T]CAGTATATACAAACA | 9886 |
rs771887268 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927706 | CATGCTGTATACAAA[A/C]ATTAAATCAAAATAG | 9886 |
rs771898139 | snp | C/G | | | upstream-variant-2KB, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944639 | CTGGAAAAGTAAGTT[C/G]GGCCACTAACCGGCT | 9886 |
rs771900122 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920193 | TTACATGCTAAGCAC[C/T]GAATGAGTGCCAGGC | 9886 |
rs771919845 | snp | A/C | 6.64695e-05 | 0.00576457 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886086 | CATTCATAAAGACAC[A/C]ACTATGCTTTTAGGA | 9886 |
rs771954784 | snp | C/T | 1.65784e-05 | 0.00287905 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888751 | CAGGCTCCTTCACTC[C/T]CATTTGGGGATTCTT | 9886 |
rs771978699 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984393 | GTGTTTTATGCATAT[A/G]ACTATTCTGAATGTT | 9886 |
rs772041326 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953041 | TGAAACAAGCAGGAT[A/G]CTACAGTGATTGTAC | 9886 |
rs772070918 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916779 | TGAGGGAATAGGGTT[G/T]CAGATGGAATTAAGG | 9886 |
rs772097297 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888475 | TCCATCCTGACCACA[A/G]TCATGGGCCCCATCC | 9886 |
rs772108405 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990097 | ATGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 9886 |
rs772109173 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895737 | ATCACAATGCTTAAA[C/T]GTCTTGTGGTTAACC | 9886 |
rs772136075 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939053 | ACTTGCCATTAACCT[C/G]TGTCTATGCAATAAG | 9886 |
rs772150512 | in-del | ACAC/GTGTGTGTGTATATATATGTGT | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912195 | TTCATAAATATATAT[ACAC/GTGTGTGTGTATATATATGTGT]ATATATATACACACA | 9886 |
rs772183997 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60946657 | TTTCCTCAGTTTCTT[C/T]CATTTTCTCAGTTCT | 9886 |
rs772190509 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903137 | GCAGAGAGGAATTCT[A/G]GGAGTACGTGACACT | 9886 |
rs772193532 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912216 | GTGTATATATATGTG[C/T]ATATATATACACACA | 9886 |
rs772209070 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974765 | TTTAATGTCACCTCT[A/G]ATTACTTACTGGTTG | 9886 |
rs772278027 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934564 | GTCTACTTCAAATAA[A/G]TAGAGTTTAAAGAAT | 9886 |
rs772282127 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917293 | TGGCAAATTCTATTC[A/G]TTCTTTAAAACCTTA | 9886 |
rs772292766 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996960 | AAACTTAACACTCAA[C/T]TCTTATTACTACTTA | 9886 |
rs772302334 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963116 | ATAAACAAGTGATCA[C/T]ATAAACAAACCACAC | 9886 |
rs772360710 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60967698 | GCATTCTAAATGCCT[C/T]CAGGGGTGAGAGCTG | 9886 |
rs772362003 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921980 | TGGTGGGGAGGAGAG[C/T]CCCAGTAATTGCAGG | 9886 |
rs772381721 | snp | C/T | 1.83609e-05 | 0.00302987 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889215 | TTTAAAAATTATAAT[C/T]AGCCTTGTTTTAGGA | 9886 |
rs772424708 | snp | A/G | 1.65176e-05 | 0.00287376 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875017 | ACTCGTGGCGGCTTT[A/G]GTCAACTCCTGAACG | 9886 |
rs772467830 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927245 | CATGTTCATAGATGG[C/G]AAGATCGATATTGTT | 9886 |
rs772476846 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000143 | TTAGTTAATCCTTAC[A/G]CTTCCGAGTGCATCT | 9886 |
rs772523364 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956474 | TTCATTAATAAATTA[A/G]TCTTAGGTTACTATA | 9886 |
rs772524250 | snp | A/G | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888310 | AAGGCTTCCTTGTTC[A/G]TGATGTTTTCCACCA | 9886 |
rs772538441 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903376 | TGCCCATGAGTCTAG[A/T]AACCAACCCCAGTGA | 9886 |
rs772549110 | snp | C/T | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878032 | TACTGCTTGCATTGA[C/T]ATCTTGTTTATGTTC | 9886 |
rs772576135 | snp | G/T | 1.66355e-05 | 0.002884 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886240 | TCACGTCTGCCAAGG[G/T]ATTGAGGAAACACAA | 9886 |
rs772586528 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877779 | TGATTAATTCATATC[A/G]TTCTACACAAGACAG | 9886 |
rs772593087 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982370 | AGTTCCTTCTCAAAT[A/G]ACAACAGTAACAACA | 9886 |
rs772618354 | snp | A/G | 3.32176e-05 | 0.00407526 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875086 | ATTAAACCACGCCCT[A/G]CGAGCCAGGTAGCTT | 9886 |
rs772648251 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901089 | CCTCTATTGCACAGA[A/C]CATCTTGCTTTTAAA | 9886 |
rs772666728 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928413 | ACAATAACCAAGATA[C/T]GGAATAAACCTGTGT | 9886 |
rs772684096 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889614 | AGAACTTTTCATTTA[A/C]ATGACCATGTGCCTA | 9886 |
rs772692672 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878578 | CAATGTACTACACAA[C/T]GTATACACTTCATTA | 9886 |
rs772693954 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878297 | GAATTTTTAAATGAC[C/T]ATTTGGACTTCTAAA | 9886 |
rs772724715 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985791 | CCATTTCTTTGTTAA[A/G]TATTGTAAGAAAGGG | 9886 |
rs772735627 | snp | C/G/T | | | nc-transcript-variant, intron-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:61000909 | GCATCACCTTAGGGC[C/G/T]GGGCATGAGGAGCTG | 9886 |
rs772746843 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876964 | TATCGAAAGCTAATA[C/T]GCTCAGGCACTCAGA | 9886 |
rs772769410 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955974 | ATCACAGTGGGCCTC[-/A]TTTGTTAATAGTCTG | 9886 |
rs772788679 | snp | A/C | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002302 | GACCTTCCAGTGGTC[A/C]AGATGATCTAGGCCA | 9886 |
rs772792443 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889044 | GTGCCTGCGGGAAAT[C/T]AGCGCTGCTCGGATT | 9886 |
rs772799976 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983836 | AGAGCTTCCCGGCCC[C/T]GCCCTCCTTCTGGCC | 9886 |
rs772813661 | snp | C/T | 3.30524e-05 | 0.00406511 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910980 | ACAACATCCCGAGAA[C/T]GCTCCAAGACCTGCA | 9886 |
rs772817438 | in-del | -/ATTAATTATTTTA | 0.000686408 | 0.018513 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888196 | ATTAATGGCTCTGCC[-/ATTAATTATTTTA]CCGCGGCCCACTCAC | 9886 |
rs772835087 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001081 | CGCGCGCGCACGCGT[-/GT]GTGTGTGTGTGTGTG | 9886 |
rs772843293 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969596 | GAGAGACAGATTATG[A/G]CTCAATTAGGATTTT | 9886 |
rs772880434 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918271 | GGGACAGAGCCAAAT[A/G]TGACCTTAGTTAGCC | 9886 |
rs772924029 | snp | C/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912192 | TAATTCATAAATATA[C/T]ATGTGTGTGTGTATA | 9886 |
rs772932391 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929641 | GAAAAATTATCTGCC[A/G]GAGATAATCTAGAAG | 9886 |
rs772936208 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908990 | GATAATGGGTTACAG[C/T]TGACAGAACCAAATG | 9886 |
rs772951902 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878279 | CTGACACAGCCTGAT[A/G]TGGAATTTTTAAATG | 9886 |
rs772989976 | in-del | -/TAT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924241 | AATGATACGAATGAC[-/TAT]TATAAATTTCACCAA | 9886 |
rs772998964 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897817 | GTTCAAGCAACTCTC[C/T]TGCCTCAGCCTCCCG | 9886 |
rs773004235 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963026 | TTGTAATACAGACCA[C/T]GGCTACAGATGTGAT | 9886 |
rs773006432 | snp | A/C | 1.95865e-05 | 0.00312936 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911331 | CCCTAGGGATGCTGA[A/C]GACACTCTGTGCATC | 9886 |
rs773068196 | snp | A/C | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886168 | CTGCCATCCACTCAC[A/C]GCTACAGATCAGCAG | 9886 |
rs773088060 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993194 | CACCAGCTCCATCTC[G/T]TCTTACTGGTGTAAT | 9886 |
rs773163573 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900273 | AGGACCAATTAAGAG[A/G]TAAGAATTCCGAGAG | 9886 |
rs773168313 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938093 | AGCTTGGAAGGGTTT[A/G]TGTAACAAAGACAGC | 9886 |
rs773169397 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981408 | GCCTGTTAAACAGAT[A/G]AAGAAACTGAGTGCA | 9886 |
rs773169595 | snp | A/G | 1.65244e-05 | 0.00287436 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875032 | GGTCAACTCCTGAAC[A/G]GCATGCTGTTCTGGG | 9886 |
rs773169902 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951321 | TTAATTGGCACCACC[A/C]CTCCTTTCATAATGG | 9886 |
rs773191621 | snp | A/G | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874790 | CCAGCAGGCTGAATG[A/G]TACATAAAAGGTAAA | 9886 |
rs773223829 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873524 | TGTAGTGGGTGTGTA[A/T]GGGGGTAAGGTGGGA | 9886 |
rs773252697 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60984652 | AGAAGGATCAGCAAA[C/T]TTTATTCTTTAAGTT | 9886 |
rs773288272 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930888 | ATTCCCTCCGACAAA[G/T]AAACGAATCTTTCTT | 9886 |
rs773290784 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875398 | CAGCTCCTCATTCAC[A/G]CTAGCCACAGTAAGT | 9886 |
rs773333654 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875869 | AGGGCTGTCACCTGC[C/G]TCTGAGACTGACGTG | 9886 |
rs773374314 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983500 | AAGTGTCATGCTTAT[C/T]CTGATTTTAGGATAT | 9886 |
rs773382435 | snp | A/G | 1.66203e-05 | 0.00288268 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874912 | AGCATTAAATGAACT[A/G]ATTGAACACACTTAA | 9886 |
rs773431570 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893148 | AACATCTTGGAGTCA[C/T]GCAAACAGCCTGATA | 9886 |
rs773452417 | snp | C/G | 3.29625e-05 | 0.00405958 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888353 | CGAACATCTCGAGGA[C/G]CTCTGCGATCTGAGC | 9886 |
rs773459494 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933586 | TTAGCTGGGTGTGGT[-/G]GCACGTGCCTGTAGT | 9886 |
rs773490532 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60977823 | CTGCCTTTAAAACAT[G/T]CATATATAATTGGAT | 9886 |
rs773513865 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999179 | TAAAGGAGGAGTGGC[A/G]GCAGAGGGAAGGTTG | 9886 |
rs773602548 | snp | A/T | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942335 | ACATCAAACTGTTAC[A/T]TGTGTTTCTATTTCC | 9886 |
rs773603914 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61001630 | GGACCACGGGTCCCT[C/T]CACATCCTCGCGGCC | 9886 |
rs773615210 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935984 | CTTTATTGTTCTAGA[C/T]CTAAGAAAATAATTT | 9886 |
rs773625048 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913604 | CACTGCAGTGTCTGG[A/G]AACGTGTCTGGTTGT | 9886 |
rs773641552 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964424 | ATCATCTCATCCAAT[C/T]AACTTGTATTAAGGA | 9886 |
rs773651489 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60942359 | TATTTCCACCTGTGT[A/G]ATCACAGAGCCTGTG | 9886 |
rs773659381 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978560 | GATCTGCAGTGTAAA[C/G]CCGTGCTGGGACAGT | 9886 |
rs773688807 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988273 | AGTTATATTTATTTA[C/T]TTCAAAGAACTAAGA | 9886 |
rs773707262 | snp | C/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002494 | AATCATTGGAAATAA[C/G]ATTAGAAAATTATCT | 9886 |
rs773721414 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880995 | CTCAAATCCCATCTT[C/G]AATTATAGCTCCCAT | 9886 |
rs773732928 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60923417 | CAAATGAAATATAAG[A/G]TCACCAAATTGAAAG | 9886 |
rs773760392 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871455 | TTACCGATTGGTTTC[G/T]GTTTTTTGTTTTTTT | 9886 |
rs773764355 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988481 | TATCTAGTAGTCCCC[A/C]GTGTCTGTTGTTCCA | 9886 |
rs773765150 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965539 | TTCAATACATATTTG[C/T]AAGAGAATTAATTGG | 9886 |
rs773801315 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918400 | ATGAAAGAGACTCCC[A/G]GGAAGTTCTGCGCAT | 9886 |
rs773825770 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911470 | AGCGCGTCTTCCCCA[C/T]GGCATTGTCACCCAC | 9886 |
rs773844848 | snp | C/T | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871577 | CTCGTTCCCTTTTCA[C/T]ACGCTGGTAGTGATC | 9886 |
rs773853154 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907222 | TTACCAGTGTAAGAA[A/C]AGACTAATACAGGGA | 9886 |
rs773889024 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906666 | AGGACAGGACACATG[C/T]AGCACGTAGCACAGG | 9886 |
rs773935027 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60869714 | TTTTATGGTGGGATA[C/T]ATGTCAATTCTTCCA | 9886 |
rs773943962 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958925 | ATATTTAAATAAAAA[G/T]ACTTCATTTTTGTAA | 9886 |
rs773953081 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879957 | ACAGACTTTTTTCTT[C/G]TCATTATTCCCTAAA | 9886 |
rs773991830 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989489 | TAAATGTTTACTCAG[A/C]CTTATCTCTCTCCAG | 9886 |
rs774003349 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981739 | TTACTAACAGCAAAA[C/G]TTAAAAAATTAACAG | 9886 |
rs774019229 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907215 | GTCTTTATTACCAGT[C/G]TAAGAACAGACTAAT | 9886 |
rs774033799 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936129 | AGCAAGGAAGTGATT[C/T]CCATCATGGATGAAT | 9886 |
rs774049453 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963865 | GTTCTTAGACTATTA[C/G]GTAACTCCTCAGTGA | 9886 |
rs774072875 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900325 | GCCTGGGAGGGGTCC[C/T]CTACAGGTGGAAGTG | 9886 |
rs774131417 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949378 | AAGAATCTGTGTGTT[C/T]GTAGTTTTTGCACTT | 9886 |
rs774141871 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974556 | CGAGATTGGGGGGTC[A/T]GTACAGAACACCCAT | 9886 |
rs774151284 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925016 | GCTTGAGCCATCCTC[C/T]TGGTGATAAGTGAAC | 9886 |
rs774164775 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874299 | AAGAGGGCTTACACT[C/T]TTCAGTGCTCGCTCT | 9886 |
rs774180426 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948206 | GAGTTTAAAAAAATA[A/C]ATTCTGGGGTGGTAG | 9886 |
rs774208167 | in-del | -/ACTG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975559 | AAATACTAGGTAATA[-/ACTG]ACTAAGTGCTGTGCT | 9886 |
rs774215574 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949746 | GCTAACCTAATGGAT[A/C]TATTCTTGGCATTTC | 9886 |
rs774246790 | in-del | -/AC | 3.53154e-05 | 0.00420196 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889196 | TGGGCCTGAAATAGA[-/AC]ATTTTAAAAATTATA | 9886 |
rs774251217 | snp | A/G | 6.60055e-05 | 0.00574442 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878016 | TATAGAGATAATCCA[A/G]TACTGCTTGCATTGA | 9886 |
rs774289767 | in-del | -/TTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987920 | TCTGAAATACTCAAC[-/TTTT]TTTTTTTTTTTTTTT | 9886 |
rs774295991 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910902 | CTGCCATATGCAAAG[C/T]GTCTGTCTTTGTGAT | 9886 |
rs774302403 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940596 | CAGATTCAAACAGCT[A/C]ACAATTTTGGGTTAC | 9886 |
rs774302536 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928484 | ACAACATGGATGGAA[C/G]TGGAGGATATTATGT | 9886 |
rs774385920 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974503 | TCCAAAAAATATACA[C/T]AGCTAAATGATTAGA | 9886 |
rs774391689 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895693 | ACAGGCGCAAGCCAC[C/T]GCGCCCGGCCCAAGA | 9886 |
rs774428256 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958155 | CAAGCACCTCTAAAG[A/G]AAAGAAATCATAAGG | 9886 |
rs774438530 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60901242 | TCTAGGCTGAGGGCA[A/G]AGGCATTTTTGGGGG | 9886 |
rs774473682 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903624 | GAAACGTTTCTTGCT[A/G]GAAAAAGATATAAAC | 9886 |
rs774511040 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876952 | TCAACAAATATTTAT[C/T]GAAAGCTAATATGCT | 9886 |
rs774586851 | snp | A/C | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883011 | TTATCCCCATTTTAC[A/C]GATGAGGAAACAGGT | 9886 |
rs774589710 | snp | A/G/T | 4.94436e-05 | 0.0049719 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888360 | CTCGAGGACCTCTGC[A/G/T]ATCTGAGCCAGGCCC | 9886 |
rs774612414 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985698 | TAAAAAACGAAATAT[A/T]TCTATTTTTTGTGAA | 9886 |
rs774624421 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995016 | GAGTAACATTGTACT[C/G]CATGGCTTGGAAAAT | 9886 |
rs774639950 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894515 | AGTGAAATATTCTGC[A/G]CTCAGTCTTACTTAC | 9886 |
rs774651613 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965695 | TTCTTGGCAATTCTT[A/C]AGGATTTTTCCATTA | 9886 |
rs774651693 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980617 | TTTGGATTAATTGTA[A/G]ATGTTTTATTTTCAA | 9886 |
rs774668654 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875546 | TCTAGACTTTAGACA[C/T]GTTCCTGTTTGACAG | 9886 |
rs774683570 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920748 | CCTACCTCCACCTCT[C/T]GGCTCAGGCCATCCT | 9886 |
rs774684522 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960810 | TTGGCAGCTACCTTG[G/T]TGCTTACCACTGCTA | 9886 |
rs774690358 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978975 | GTCTGAAACACTGCC[A/G]AATCTCCCCCTATGT | 9886 |
rs774695964 | snp | A/G | 1.6549e-05 | 0.0028765 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874945 | GGTAAAAAGCAAACT[A/G]TTACAAACCTGAGCC | 9886 |
rs774742283 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925610 | AAATTGAGATAAAAA[C/T]AGAAAAAATCAACAA | 9886 |
rs774743576 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954767 | AATAAAAGGAGATAA[G/T]TTGGTCAAGTAACAT | 9886 |
rs774775944 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895459 | GCCCAGGCTGGAGTG[A/C]ACTGGCATGATCTCA | 9886 |
rs774807662 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965792 | TTATGATGGTAACCT[C/T]TAACCATCCATCCTA | 9886 |
rs774808906 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913916 | GTGAGGATTACGTGA[A/C]CTGATGAATTAAGTC | 9886 |
rs774811069 | snp | C/T | 1.70586e-05 | 0.00292045 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889181 | TATCCCCTCTCTTTA[C/T]GGGCCTGAAATAGAA | 9886 |
rs774853410 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886971 | TCCTAAATAACCATA[C/T]TATGATTACACCTAA | 9886 |
rs774881796 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996407 | CCAGCTAAATTCTAC[G/T]GCTCTTTAAGGCCTA | 9886 |
rs774891816 | snp | G/T | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882617 | TGATTTTCATGGTGT[G/T]GGGGGTGGGAGGGTG | 9886 |
rs774898794 | snp | A/G | 1.64732e-05 | 0.0028699 | stop-gained, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889055 | AAATCAGCGCTGCTC[A/G]GATTGCATTGTCAAA | 9886 |
rs774924161 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60999286 | AAATGGACAAGTGTC[-/A]AAAAAAAAGACATCC | 9886 |
rs774929198 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997934 | GCTGTTTATAAGTCA[A/G]AAGGCTTAGGTTCTA | 9886 |
rs774952298 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949791 | TTAAAGACAGAAGCA[-/T]TAGATACTGTGTACT | 9886 |
rs774957291 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887064 | TATCCCTAAATCGTA[C/T]TTCATAGCTTTAAAA | 9886 |
rs774977675 | snp | A/G | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888760 | TCACTCCCATTTGGG[A/G]ATTCTTCACATTCCA | 9886 |
rs774981515 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934207 | TGACCTTCTCTCTGT[A/G]TACCTTAAGAACTTT | 9886 |
rs775012209 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898987 | AACCTAATACTTGAG[C/T]CTTAGAAATGGTTGG | 9886 |
rs775070218 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940385 | TAGGGGAACAGAAGA[C/G]AGAGAAGCCTGTTAA | 9886 |
rs775087990 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927857 | ATGGGATTACATCAA[G/T]CACAGCAAAGGAAAC | 9886 |
rs775125643 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908473 | AGTCACAAAACAGGT[G/T]TGCAAACCAAACAAG | 9886 |
rs775125752 | in-del | -/ATAA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889424 | TTGTGAAGCTTATCC[-/ATAA]ATATTCCATGTTTTT | 9886 |
rs775151723 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911486 | GGCATTGTCACCCAC[A/G]ACCACACATTTGATA | 9886 |
rs775157697 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60959683 | TTTTGTCTCTGCCAC[-/T]TTCCAGTTATGTGTA | 9886 |
rs775233500 | in-del | -/AGCAGCCACGGCT | | | utr-variant-5-prime, intron-variant | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944046 | CCCCCGCCACTCAGC[-/AGCAGCCACGGCT]GCGCGCGGTCGCGGG | 9886 |
rs775254571 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60983353 | CTGAATGAAATTTGC[C/T]TATTATAAGACATAT | 9886 |
rs775267552 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899635 | ACTTATCCAGTATTA[C/T]TCATCAACCATCTAA | 9886 |
rs775271589 | in-del | -/TTTT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949666 | TTTCCAGGTGAAGCT[-/TTTT]TTTTTTTTTTTTTTT | 9886 |
rs775273962 | snp | C/T | 3.32646e-05 | 0.00407814 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888686 | TTTCTTCCTCTGGGT[C/T]GACACTCAATATCCG | 9886 |
rs775282551 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60960314 | GTGACAACCAGAACC[C/T]CCTATTGATTATGCT | 9886 |
rs775296539 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951513 | TGGTCAAGTAGTTAA[C/T]TGCATCACATGTGGG | 9886 |
rs775308142 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971963 | ACACTGGTCATTAGA[G/T]AAATGCAAATCAAAA | 9886 |
rs775309656 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60937028 | ACCAGGATAATATAG[G/T]CTATTCTAGGCCACT | 9886 |
rs775340136 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922280 | GAGTCTTGAATAAAC[A/G]AGTTCACTCTATGCC | 9886 |
rs775359500 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973001 | ATGAATCCTTAAACC[A/G]TGACTATAGAAGTAA | 9886 |
rs775420246 | snp | C/T | | | stop-gained, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892926 | CTTGATTTCTGGATA[C/T]CACATGCTTTTCACA | 9886 |
rs775426745 | in-del | -/AAAC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969202 | TCCTATGGAGGTCCA[-/AAAC]AAACAAAAAACCTAA | 9886 |
rs775432676 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918521 | GTTTGCTCAGACAGG[C/T]GCACTTCAGTGTAGG | 9886 |
rs775443874 | snp | C/G | 1.67587e-05 | 0.00289466 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888565 | CCGGTCAAAGTCTGT[C/G]TCTCAGGAACTGCAC | 9886 |
rs775446810 | snp | C/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002665 | CAGGGTAAAACTCTA[C/T]TGACAGAAGAACGAA | 9886 |
rs775447482 | snp | G/T | 7.09994e-05 | 0.00595774 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893039 | ATTGCCTTTTAACAG[G/T]TTTTTTCTTTTACCA | 9886 |
rs775476012 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883583 | AGAAGGGGAGCAATC[C/T]TCCCAGCTCTTTATC | 9886 |
rs775496529 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964251 | ACAGAAGACAGATTT[G/T]TGAGGTGAATTAGCA | 9886 |
rs775509982 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893951 | CAAAAGGATACAAAG[A/G]ATAAGAAAAGTTACG | 9886 |
rs775515296 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930864 | GTCTTATTGGCATTC[C/T]CATCCATTATTCCCT | 9886 |
rs775528079 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897966 | ACCTCGGCTTTGCAA[A/C]GAGCTGGGATTACAG | 9886 |
rs775545201 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896743 | AGGAGAAAATATCAA[C/T]ATAAAAATTTCGCTG | 9886 |
rs775561952 | snp | A/G | 0.000116253 | 0.00762319 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886087 | ATTCATAAAGACACC[A/G]CTATGCTTTTAGGAA | 9886 |
rs775566945 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951374 | GACCTCACTTCTTGC[A/G]CCTGACTCAATAATA | 9886 |
rs775594021 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935742 | TACCAAAAACAAAGA[C/T]AATAAGTACTCAAAA | 9886 |
rs775594707 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962071 | CCTCGGCCTCTTAAA[A/G]TGCTAGGATTACAGG | 9886 |
rs775598251 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895838 | GGTCTGCCATATGAA[C/T]GTAGCTCCCTAAAAC | 9886 |
rs775619879 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963206 | GGTAGGCAATTTTCA[C/T]TGCCCTCCGCTCCAT | 9886 |
rs775638201 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875022 | TGGCGGCTTTGGTCA[A/G]CTCCTGAACGGCATG | 9886 |
rs775648036 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895643 | TCCCCACCTCGGGTG[A/G]TCCACCCACCTTGGC | 9886 |
rs775653593 | snp | C/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889089 | ATCCTTGATACCAAA[C/G]TGGTCAAACACGCTT | 9886 |
rs775690944 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905873 | TAAAACACAAGCACA[A/G]CCAATCCCAGGCAAA | 9886 |
rs775704360 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987072 | CTGCACAGCCCATTT[C/T]GTGGGGCTGTGCCAC | 9886 |
rs775824089 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904918 | AATGTCTTTAAGACA[C/T]AACCAGTAATAATTT | 9886 |
rs775824921 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910516 | ACCAAACAGTCTTTC[C/T]GAAGTAGGGTGACCA | 9886 |
rs775826533 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60871587 | TTTCACACGCTGGTA[A/G]TGATCTTCTTCCTTC | 9886 |
rs775849997 | snp | C/T | 1.87954e-05 | 0.00306551 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889226 | TAATCAGCCTTGTTT[C/T]AGGAAAAAAACAGTA | 9886 |
rs775853822 | in-del | -/TTAAACT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936020 | TGTTAATAATGGAGA[-/TTAAACT]TTAAAGTGTGCTATA | 9886 |
rs775898683 | in-del | -/TGA | 1.68442e-05 | 0.00290204 | cds-indel, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888597 | TCGGCTTCCAGCCCC[-/TGA]AGAGCCTCCACCAGG | 9886 |
rs775899979 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944686 | TTCCCCCTAGGAGCT[C/G]ACCGGCCGCGGACTC | 9886 |
rs775951862 | in-del | -/CCTC | 1.65718e-05 | 0.00287848 | utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60871477 | TGTTTTTTTTCTCTT[-/CCTC]TTCAGGCCACTGCTG | 9886 |
rs775962799 | snp | C/T | 3.2975e-05 | 0.00406035 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888408 | TTCATCCAGTTGTCC[C/T]GTATAAAGAAACTGG | 9886 |
rs775993256 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914021 | ACAACAAAATTGAGT[A/C]AGGAGGAAGGCCAGA | 9886 |
rs776047924 | snp | A/G | 1.64972e-05 | 0.00287199 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892860 | CAGGTCGGCATAGCG[A/G]AGATCAAGCTGGCAC | 9886 |
rs776049260 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892242 | ACATTTGTGACACTT[-/A]AAAATGTAACCACTA | 9886 |
rs776055422 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980903 | CTTCCCTCTCTGAAG[C/T]AGGTTACTACATTCA | 9886 |
rs776061740 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60927267 | GATATTGTTACAATG[C/T]CCATACCACCCAATG | 9886 |
rs776084284 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878333 | CAAATGGACTGGAAA[C/T]GTATGATGACATTAG | 9886 |
rs776192454 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951344 | ATAATGGTTCCTAAT[-/C]CTAAAAGCAAAGATG | 9886 |
rs776271100 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992699 | ATGAAACACAAATTT[G/T]GTAAATTAGAATAGT | 9886 |
rs776281328 | snp | A/C | 1.65479e-05 | 0.0028764 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888788 | CCATTAAAAACAGAT[A/C]ATAAAATTTGGAAGA | 9886 |
rs776298747 | in-del | -/CT | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884455 | CCACAAAAATGCTTG[-/CT]CACTCCTAAAGTTAG | 9886 |
rs776299624 | snp | C/G | | | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872201 | TGCAGATTTTGATTT[C/G]ATTTCCTTACGGAAC | 9886 |
rs776323027 | in-del | -/AAGT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929682 | GCCAATTCATAATAG[-/AAGT]AACATGAACCTTCAT | 9886 |
rs776335116 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998988 | CTGTGAAACACAGAC[A/G]ACGCCTGCCTCACCA | 9886 |
rs776362446 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990406 | TTTTTGAGACAGATG[C/T]AAGACATGAACACGT | 9886 |
rs776388326 | snp | A/G | 1.65616e-05 | 0.00287759 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886098 | CACCACTATGCTTTT[A/G]GGAAGGCACGTACCT | 9886 |
rs776420651 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950425 | TTTAAGGCTATCTTG[C/T]CTGACCACCTGTTTC | 9886 |
rs776450692 | in-del | -/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966441 | TTGGGAGGCCAAGGT[-/G]GGAGGATCACTTGAG | 9886 |
rs776476395 | snp | A/G | 1.66018e-05 | 0.00288108 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60878048 | ATCTTGTTTATGTTC[A/G]GGAGATACACCTGAA | 9886 |
rs776489726 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911195 | CAGAGCCACAGTCTC[C/T]GGTTTGCATTTTGCT | 9886 |
rs776496327 | in-del | -/CTACA | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60876242 | CATGTTCTAAACACT[-/CTACA]CTAGACAGTACAAAG | 9886 |
rs776508816 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908857 | GGTACAAACATGCAC[A/G]CAAAGCAAGGCCCTA | 9886 |
rs776569882 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989065 | GGATTTTTTTCAGTC[-/A]AATATCACTGTGAAA | 9886 |
rs776590525 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886156 | CCCCGAACATGGCTG[C/T]CATCCACTCACAGCT | 9886 |
rs776593956 | snp | A/T | 1.70621e-05 | 0.00292074 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877867 | AATGTGATTTTGACA[A/T]ATATGACAGACACTG | 9886 |
rs776637835 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932006 | TATTCTGTGGCAATC[A/T]ATTGTAGTTAAAGAT | 9886 |
rs776641460 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920709 | GGCTAGAGTGCAGTG[A/G]CACAATCTCGGCTCA | 9886 |
rs776643927 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990988 | CACCATTGTTCCCTG[A/G]CACTTCCTCATGGGG | 9886 |
rs776651303 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60995841 | TTTTTTCACTTCCCC[C/T]AAGATAAAAAAAAAA | 9886 |
rs776656151 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871231 | GTTTATTAAGCCTCC[A/T]AACAAAAAAAATATA | 9886 |
rs776674265 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910913 | AAAGCGTCTGTCTTT[A/G]TGATGATCACCAAAA | 9886 |
rs776676893 | snp | C/T | | | intron-variant, missense | RHOBTB1 | GRCh38.p7 | 10:60885824 | CTTCATGGATGAGGA[C/T]GGCTCTGAGGATGAA | 9886 |
rs776689525 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873745 | CTTGCTGATTCGACT[A/G]CATTAGATGTCTATT | 9886 |
rs776700319 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940679 | TTCTGGATGACTACA[C/T]AATCTCTCCCTGTTG | 9886 |
rs776707585 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899294 | AAGGCTTGCTAAACA[A/G]ACGAAGGTGAAATTG | 9886 |
rs776713370 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976513 | GTTCCTTTTATAGCC[A/G]GTCTTTATGCAAGAA | 9886 |
rs776779432 | in-del | -/TAT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930457 | CCAGAGAAATGCTGC[-/TAT]TATTGAGGGGAAAGT | 9886 |
rs776780009 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60908289 | AGGTCTAAAACATGT[C/T]GGTTTAAATCTGGCT | 9886 |
rs776797075 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994623 | TGAGGGAAAGATATC[C/T]TCAGGAAAAAAAATG | 9886 |
rs776800627 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951424 | TTTCAGAGTATCCTT[A/G]GCTCTGTAAATATTT | 9886 |
rs776802326 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957829 | ATCTCCTTTACCATT[C/G]CCACTGTACGGACAG | 9886 |
rs776807591 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897851 | AGCTGGGATTACAGG[C/T]GCATGACCATGCCTG | 9886 |
rs776834506 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879358 | TCTTTTTTATTTTAG[G/T]TTTTTTGAGACAGGG | 9886 |
rs776894957 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939536 | CCATCTCCTACCCTT[A/G]TCTACACACACTTTT | 9886 |
rs776904891 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60966692 | TTTTTTTTAATCTTT[-/A]TTTTTTTTACTATAC | 9886 |
rs776908879 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997771 | AAAAATAGGTTATAC[A/G]TACTAAGATGTTCTA | 9886 |
rs776922284 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911695 | AATGTTTGGAAGTTC[A/G]TACTAAGCCTAATTG | 9886 |
rs776947927 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60975647 | GAAAAATCATGAATA[C/T]CTGATTATACATAAA | 9886 |
rs776953918 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896918 | AAAAATGCCTGAGCT[A/G]ATAAAGCCAAGCTCA | 9886 |
rs776957867 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000680 | CTTCATTTTTTTTTA[A/C]TTCCCAAGTGTTAAA | 9886 |
rs776962652 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930953 | TTTAATATGTGACTA[-/T]TTAACATTTAATAAC | 9886 |
rs777034927 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60986207 | CTTTAAGTACTTAAC[A/T]TCCTGGTGATGCTTC | 9886 |
rs777065584 | snp | A/G | 1.69215e-05 | 0.00290869 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888217 | GCCCACTCACCCGAG[A/G]ACGTTCCCTTGCTGA | 9886 |
rs777070841 | snp | A/T | 0.000131846 | 0.00811822 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888335 | CCACCATCATCCTCA[A/T]ATCGAACATCTCGAG | 9886 |
rs777098850 | snp | G/T | 4.94222e-05 | 0.00497078 | missense, nc-transcript-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872239 | ATACACTGTTGTAGT[G/T]GGTGCAGATGTGGTG | 9886 |
rs777108468 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60905150 | ATCCAGATAATACTT[A/T]AAAAAAAAAAAAAAT | 9886 |
rs777190813 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898083 | TTCTTTTGTTCCATG[C/G]TAGGATCCCACCTCT | 9886 |
rs777192982 | snp | A/C | 3.31576e-05 | 0.00407157 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875077 | CAGGAGAACATTAAA[A/C]CACGCCCTGCGAGCC | 9886 |
rs777227897 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60871184 | CTGAATTTTTTTTCT[C/T]TGTATAAAAAGAAAC | 9886 |
rs777258890 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930563 | CCTCATGCATTCACA[C/T]GAAGCACTGTCTTAG | 9886 |
rs777326968 | snp | A/G | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869150 | ACTAAGTCCTGTAGG[A/G]TAGTTCTAGTTTCTC | 9886 |
rs777356720 | snp | A/G | 1.66927e-05 | 0.00288895 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889167 | TTCTGGGGGCAAAAT[A/G]TCCCCTCTCTTTATG | 9886 |
rs777365199 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886481 | AGAAAGTAATAGAAA[A/G]GAGGGAATATTTTTT | 9886 |
rs777371483 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926524 | ACACACTAAAAAGAT[A/T]ATTCATCATGATCAA | 9886 |
rs777378844 | in-del | -/TACT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928837 | ATGGAAACCCCAATG[-/TACT]TAGTAGTCTGTTCTC | 9886 |
rs777391853 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982945 | GGAAAGGCGGTGCAC[A/G]TGACATAAGGCACAG | 9886 |
rs777448889 | snp | C/T | 1.66382e-05 | 0.00288424 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892831 | AACGGGCGCCTGGCT[C/T]GATTAACAGCTTCCA | 9886 |
rs777455450 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874229 | AGAGTGTAAATTCAT[C/T]GTTAATCAGCCTGTG | 9886 |
rs777482916 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976521 | TATAGCCAGTCTTTA[C/T]GCAAGAAGTCTGAAA | 9886 |
rs777494924 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60880138 | TCTGAGTTGGGGGGG[-/T]GGTCCTGGAACCAGT | 9886 |
rs777511393 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994434 | ATATTCCAGAGAAAC[A/G]TAACAGCTAATAATG | 9886 |
rs777525059 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971604 | ACCCTAGAAGAAAAC[C/T]TTGACAATACCATTC | 9886 |
rs777532018 | snp | C/T | 5.18883e-05 | 0.00509328 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911351 | CTCTGTGCATCTTAC[C/T]TCCTGGCACACGCGG | 9886 |
rs777547474 | snp | C/T | 1.65734e-05 | 0.00287862 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886228 | CCAATTTAAATGTCA[C/T]GTCTGCCAAGGGATT | 9886 |
rs777563349 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994613 | TTTTCTAATGTGAGG[A/G]AAAGATATCCTCAGG | 9886 |
rs777563892 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925294 | TCAGGTATTTCTTTA[-/T]AGCAATGCAAGAAAA | 9886 |
rs777578192 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60972716 | AGAGAAAACTAATAA[C/T]CTAATTGTTGTGCTT | 9886 |
rs777607433 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60964042 | ATTCATGAAAAATGC[A/G]CAAAAAAGACCTACC | 9886 |
rs777657024 | snp | A/C | 1.78857e-05 | 0.00299041 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888182 | AACACAATCAAAGGT[A/C]TTAATGGCTCTGCCC | 9886 |
rs777657721 | snp | C/T | 1.92165e-05 | 0.00309966 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871667 | CTGGTGAAGGAAAGA[C/T]GCAGACCATAAGACC | 9886 |
rs777663492 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896554 | AAAAGGGGTAGGAAG[A/G]AGTTTGGAATGTTTA | 9886 |
rs777664469 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911533 | TTTCGTAGTCCATGT[C/T]AGCGTCCATTTATGA | 9886 |
rs777714850 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60915211 | AATTTTATCCTTCTC[C/T]GCTTGTTATAGGCTC | 9886 |
rs777718130 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871698 | TGCGGTTCATTGATG[C/G]CTTTTATGTGCTAGG | 9886 |
rs777749064 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60965015 | TCTGCCTTTGGGAGA[C/G]AATTTCACAACTTTA | 9886 |
rs777754426 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911458 | TGGCACAGATCAAGC[A/G]CGTCTTCCCCACGGC | 9886 |
rs777774851 | snp | A/C | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886132 | TGTTGGCACTTTCCA[A/C]AAATGACCCCCCGAA | 9886 |
rs777866623 | snp | A/G | 1.66255e-05 | 0.00288314 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886082 | CATACATTCATAAAG[A/G]CACCACTATGCTTTT | 9886 |
rs777888324 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60925439 | TGCACAAATGGTACT[C/G]AGAGGAAAGTTTATT | 9886 |
rs777888817 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60954964 | TGTGAAAGTAAATTA[C/T]GCATTTATAAGAGGG | 9886 |
rs777928595 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60877453 | TTACAGGACAAAGTC[A/C]CCTGGTCAGTAAATG | 9886 |
rs777975743 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926576 | TAAGGATGGTTCAAC[A/T]TATGCAAATCAATAA | 9886 |
rs778022175 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60968459 | AAAAATAGCAGGATA[C/T]CTCTTATGTTGCAGA | 9886 |
rs778036579 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955855 | CTATCACGATTGATG[A/G]AGTATTTTTCATTTA | 9886 |
rs778058190 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918949 | TGGGGTTTCTCCATG[C/T]TGATCAGGCTGGTCT | 9886 |
rs778113593 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950051 | TCTGCAACTCTAACT[G/T]CAGTCTTTCTGTCAA | 9886 |
rs778118520 | snp | A/C | 0.000115978 | 0.00761415 | splice-donor-variant, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910885 | TACTAGTCTTGGTTT[A/C]CCTGCCATATGCAAA | 9886 |
rs778149644 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989390 | ATGGTAGATTTTCCA[C/T]GAGGGACGGAAAATG | 9886 |
rs778219030 | snp | C/T | 1.66785e-05 | 0.00288773 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888539 | GCATGCCAATGAACC[C/T]CTTACTCCATCCGGT | 9886 |
rs778223753 | in-del | -/G | 3.43696e-05 | 0.00414531 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878107 | CAGAAAGCAGGGAGT[-/G]GGCACATTTTCAGGC | 9886 |
rs778223902 | snp | C/G | 0.000684132 | 0.0184824 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60888198 | TTAATGGCTCTGCCC[C/G]GCGGCCCACTCACCC | 9886 |
rs778247865 | in-del | -/C | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003116 | TTGGTGTGTGATGTT[-/C]CCCCTCCCTGTGTCC | 9886 |
rs778255914 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979928 | TGAAAAGGTCATAAG[A/G]CAGAAACACACTATA | 9886 |
rs778306728 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888430 | AGAAACTGGAGCAGG[A/G]TCCGAAAAGGGCCTG | 9886 |
rs778310676 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, missense | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60944292 | GAGCACCCGGCACCT[C/T]GCTCCGCCGCCGTGG | 9886 |
rs778316577 | in-del | -/GGT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921960 | TTCACCAAATGGGAA[-/GGT]GGTGGTGGGGAGGAG | 9886 |
rs778334665 | snp | A/G | 1.65138e-05 | 0.00287343 | missense, nc-transcript-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60875009 | CCCACGCCACTCGTG[A/G]CGGCTTTGGTCAACT | 9886 |
rs778349197 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920270 | GTGGAAAGAAACAAG[C/T]AAACAGGTAGACAAA | 9886 |
rs778360929 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60894878 | CTTAATTTATATGAC[A/G]GACATGTAGCTAAAT | 9886 |
rs778393675 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973968 | AAGATGGAAGAATGA[A/C]CTTATTAAACTAAAT | 9886 |
rs778397227 | in-del | -/TT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60932507 | TACTTCAATACTTTC[-/TT]AAAGTAAAAAAAAAA | 9886 |
rs778400667 | snp | A/G | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60945955 | GAGGCCGAGGCGCGC[A/G]GATCACGAGGTCAGG | 9886 |
rs778431162 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60907010 | CATGACAGTGAATAA[A/G]TATCATGAGATCTGG | 9886 |
rs778446288 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985201 | AATACAATGAAGAGT[A/G]AAAATAACAAATAAT | 9886 |
rs778460529 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930732 | ATGTTTCCCTCTGGA[G/T]TCTCACCTTTCATGG | 9886 |
rs778466947 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886505 | ATTTTTTCCTCCTTG[C/T]TATGCAAAACTTCAA | 9886 |
rs778547633 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943149 | CACAGCTTGTGTGCT[A/G]ACGTGCAAAGCGAAG | 9886 |
rs778568920 | in-del | -/TGTA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982289 | ATAGGCCTGACTAAC[-/TGTA]TGTACTGGGATGGGC | 9886 |
rs778618696 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888297 | CTCCTGGTTCATGAA[A/G]GCTTCCTTGTTCATG | 9886 |
rs778628585 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60936486 | TTACCAGGTCATCAC[C/T]GCCTACATCCCTCCT | 9886 |
rs778692865 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60961289 | CAGTATGCCTAGAGC[C/T]GGACACATCTGGATT | 9886 |
rs778696269 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888876 | CAGAACATCGGCACA[C/T]AGAGGATTGTCCAGT | 9886 |
rs778710017 | snp | C/T | | | | | GRCh38.p7 | 10:60898302 | TGCTGGTAACTGAGG[C/T]AGGTTCTTTACAGAA | 9886 |
rs778718269 | snp | A/G | | | | | GRCh38.p7 | 10:60995567 | TGGCCAAAAAAGATG[A/G]CAAACCTGCTATTAA | 9886 |
rs778744322 | snp | G/T | | | | | GRCh38.p7 | 10:60960175 | ATTTAATCTTGGTAA[G/T]GTACCAATGATTTCA | 9886 |
rs778766939 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996925 | ATCTGGAGAACAAGG[A/G]ACTTCACTATTTCCT | 9886 |
rs778772204 | snp | G/T | 1.65902e-05 | 0.00288008 | splice-acceptor-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60911554 | CCATTTATGAAACTC[G/T]GTAAGAAGAGAGTGA | 9886 |
rs778796078 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60956438 | GGCTACACTATATTC[A/G]TAAGATAATATTTTT | 9886 |
rs778823212 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924401 | AAGACAAAAACTGTA[A/G]AAAGAGACAAAGAAG | 9886 |
rs778847569 | in-del | -/AC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879803 | TGCACTTGCACACAA[-/AC]ACACACACACACACT | 9886 |
rs778853549 | in-del | -/CTC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60874001 | TTGCACCAGAGCAAT[-/CTC]CTCTGGCCACAGTAG | 9886 |
rs778879355 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929833 | GAAATAAACAACACA[C/T]GGAGGATCTGAATAA | 9886 |
rs778897954 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60987839 | ACTATCAAATGCTCT[C/T]CACCCCCTAACCCCT | 9886 |
rs778942278 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913606 | CTGCAGTGTCTGGAA[A/G]CGTGTCTGGTTGTCA | 9886 |
rs778954090 | in-del | -/CT | 1.90087e-05 | 0.00308285 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911336 | GGGATGCTGAAGACA[-/CT]CTGTGCATCTTACCT | 9886 |
rs778958732 | snp | A/G | | | downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60869328 | TGCTTTGTTACTGGA[A/G]CATGCACAAGCCCCC | 9886 |
rs778984486 | snp | C/T | 3.2994e-05 | 0.00406152 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911387 | GTCAATCGCCCACAC[C/T]GTTGGCACGTGGGTG | 9886 |
rs779003470 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912472 | TCCTTATCTCAAGTG[A/G]TCTCCCCACCTTGGC | 9886 |
rs779026713 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969969 | CAGTTCTGATGTCAG[C/T]AAGGAGAGAACTGGC | 9886 |
rs779078571 | snp | A/C | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886204 | TGTGGGCACTGATGG[A/C]TCCATCGTCCAATTT | 9886 |
rs779104100 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60878245 | GTTTGATTTGTAGTT[C/G]ACAAAAGAGTGGAGC | 9886 |
rs779114613 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916656 | CAACTTTTCTCTTTA[C/T]AGTCGCCCTCAATTT | 9886 |
rs779142114 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899434 | GAGGGCAAGTTGCAC[A/G]CATAAGAAAACTTCA | 9886 |
rs779165417 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889343 | CAAGTCTTTGAACTA[C/T]AAAGGAGTTATGATT | 9886 |
rs779229358 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871890 | ATTTCAGAGTCTAAG[C/T]CTGCTCCTAAGCTTG | 9886 |
rs779249340 | snp | A/G | 1.68826e-05 | 0.00290534 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911031 | TGCTCGGTGTCAGTC[A/G]GAAGTTCCCCAGGAG | 9886 |
rs779259634 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60917165 | AGCAGCAATAAGAAA[C/T]TAACGTAGCACACTT | 9886 |
rs779294922 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980087 | AGCAAAATTATATGA[C/T]TTATACTTTATTGAA | 9886 |
rs779296218 | in-del | -/TGTGTGTGTG | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912194 | ATTCATAAATATATA[-/TGTGTGTGTG]TATATATATGTGTAT | 9886 |
rs779303073 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921154 | AGTTTCACCATGTTG[A/G]CCATGCTGGTCTTGA | 9886 |
rs779324973 | in-del | -/TTTAT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60990501 | ACTTAGCAATTTCTC[-/TTTAT]TTTATTTTAATTCAA | 9886 |
rs779339669 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948806 | AATAACACCCAACAA[C/G]TTTCTGGCTTCCTAA | 9886 |
rs779358286 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60913933 | GATGAATTAAGTCCT[-/C]CAGTGCCGTAACTGA | 9886 |
rs779382302 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992001 | GTGTCTAACACATAG[C/T]AGATTATCAATAAAG | 9886 |
rs779420106 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900040 | CCGAGGTAGGAGCCT[A/G]CCTGTGGTGCCCTCC | 9886 |
rs779425981 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924429 | AAGGTCATTATATAA[-/T]GACAAAGGGGTCAAT | 9886 |
rs779442785 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60926958 | CTTGGTTGCAGATGA[C/T]ATCTTATATTTAGGA | 9886 |
rs779470409 | snp | A/G | 1.64841e-05 | 0.00287085 | stop-gained, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888404 | CCTTTTCATCCAGTT[A/G]TCCCGTATAAAGAAA | 9886 |
rs779546152 | snp | A/G | 1.65389e-05 | 0.00287562 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877932 | CAACCAAGTGTGGCA[A/G]GCAAAATCTGTTTGC | 9886 |
rs779558389 | snp | G/T | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888312 | GGCTTCCTTGTTCAT[G/T]ATGTTTTCCACCATC | 9886 |
rs779561110 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60991727 | TGAGCCACCGCACCC[A/G]ACCTTCCCTCAGTCT | 9886 |
rs779581261 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60950874 | ACTGTAAGTATTATA[C/T]ATAAAAGCTTCCACC | 9886 |
rs779592967 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60920487 | AGGAAGTGGGGAAGC[C/T]GGAAGGTTAGAAAGG | 9886 |
rs779637106 | snp | A/C | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884684 | TTCTGTCATTCAAGA[A/C]AACATGCATGAACCT | 9886 |
rs779667108 | snp | A/G | 1.65083e-05 | 0.00287296 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60872311 | GAAAAGTGAGCAAAA[A/G]GAGGGTAAGACTATT | 9886 |
rs779675962 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933242 | TAGGTAGAAATTATT[A/G]CATGAAAGATTGTAC | 9886 |
rs779683183 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60921335 | AGGGGTGCAATGGCA[G/T]AGGAATGGTGAGGAA | 9886 |
rs779686049 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60896473 | GGGTAAAAAGCATAA[G/T]AATTCGAGAATGCAG | 9886 |
rs779707565 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60914855 | TCCTCTAATCCCTAG[C/T]AGTCCGCTCCAGACC | 9886 |
rs779737199 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895362 | CTATGAGAATCTGTG[C/T]TCATTATTTTACACT | 9886 |
rs779758199 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60998348 | TTCATCACTGTGCTA[C/G]GCCCTGGGAATACAG | 9886 |
rs779796195 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992511 | ATTCTGCTGGATATG[C/G]CTTTTTATATCTTAG | 9886 |
rs779828069 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60931702 | TTGTTTTTTCAAAAC[A/T]ATATGTATATATAAA | 9886 |
rs779880997 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943640 | GGGAAGCGCCTTCTC[A/G]TCGGCGCGGCACCAC | 9886 |
rs779886462 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60997476 | TATAAAATGTAATAC[C/T]TTAGCAAGGATTGCT | 9886 |
rs779909004 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888885 | GGCACATAGAGGATT[G/T]TCCAGTAAACAGGCA | 9886 |
rs779910974 | snp | C/T | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:60946254 | AAGCCTTAAACAAAA[C/T]ACATTCTTTTCAGGT | 9886 |
rs779917480 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60887748 | AGATCACTGATTTTT[A/G]TCATGGGTCAGTGCT | 9886 |
rs779919751 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888997 | AGTAAAGGTTTCTGG[A/G]CTTTCTTTAGGTGGG | 9886 |
rs779973552 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60974054 | GTCATCAGAATTTTC[C/T]ATCTCCATAACATGA | 9886 |
rs779987174 | snp | G/T | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002005 | AAGGATTCCATCAGG[G/T]GGTTCTGCTGACATC | 9886 |
rs780027244 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953432 | TGGCATTTGTGTGGA[A/G]TGAATACCAAATGAG | 9886 |
rs780040631 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988140 | GGGATTTCACTGTGT[A/T]AGCCAGGATGGTCTC | 9886 |
rs780040837 | snp | A/C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958638 | AAAAGGGGTCTCACT[A/C/T]GGTTGCCCATGCTGG | 9886 |
rs780045712 | in-del | -/TG | 1.65526e-05 | 0.00287681 | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60874944 | AGGTAAAAAGCAAAC[-/TG]TTACAAACCTGAGCC | 9886 |
rs780113975 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941433 | TGCTCAATAAGTCAA[C/T]TATTACTATATCAAG | 9886 |
rs780114347 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant, utr-variant-5-prime | RHOBTB1 | GRCh38.p7 | 10:60911424 | AGCTGATACTGCGTG[A/T]GTGTGGTGTTGCACG | 9886 |
rs780191612 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60897700 | AAGCTAACAATTACA[A/T]ACATATACATATAAT | 9886 |
rs780205480 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919387 | CCAACAGCCAAGTTT[C/T]GATTGTGCAGATTTC | 9886 |
rs780225078 | snp | A/C/G | 3.69148e-05 | 0.00429608 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60871655 | ATTCCTGGTTGTCTG[A/C/G]TGAAGGAAAGATGCA | 9886 |
rs780267275 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60889615 | GAACTTTTCATTTAC[A/G]TGACCATGTGCCTAA | 9886 |
rs780276552 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60947748 | AGGATATTTGAGTAG[C/T]TTCCAGTATTTTGCT | 9886 |
rs780300571 | snp | A/C/T | 0.000365694 | 0.0135179 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60875087 | TTAAACCACGCCCTG[A/C/T]GAGCCAGGTAGCTTG | 9886 |
rs780307001 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:61000122 | AAGCATTTTACAAAT[A/C]TTTTATTAGTTAATC | 9886 |
rs780314187 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877954 | TCTGTTTGCCAAGGC[A/G]ATTAATTCCAGCGGG | 9886 |
rs780322422 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900093 | CTGCTGGAGCACAGT[C/T]GTGAGGGGAAACTGA | 9886 |
rs780332365 | in-del | -/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979585 | TTCAATTCAATTTAA[-/C]CAATACCAGGCACTG | 9886 |
rs780334843 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969150 | TGAGATGGAACAAAT[G/T]TAATGAGGTAACATT | 9886 |
rs780388277 | snp | A/G | 1.67916e-05 | 0.0028975 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888645 | CCACTGGTCGGCCTG[A/G]GGAATCCTAGGCGGG | 9886 |
rs780411834 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60976447 | CACTCACAGGTCAAG[A/T]GTATCTAACTCCGAG | 9886 |
rs780430504 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60978434 | ATCAAGTGGAAGTTA[C/T]TAACATGATTTGGTC | 9886 |
rs780433863 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911066 | GTGTTCAAGTCAGCA[C/T]CCTCAGTGCCATCAA | 9886 |
rs780441042 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60971063 | TTTATGGGACACTCT[C/T]ACCATCATCATTATC | 9886 |
rs780449600 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900595 | TCTCTCTCATTGTGC[A/G]CACACAGTGTAAGGA | 9886 |
rs780484368 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60928471 | CCTGTTGTTTGAAAC[A/G]ACATGGATGGAACTG | 9886 |
rs780519555 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982068 | GAGCCACTGTGGCTG[G/T]CCTGTAAGTTACTTT | 9886 |
rs780524047 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60957724 | CTGCTTCTGAATAAC[A/T]GAAAGAGATTCATAA | 9886 |
rs780539912 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890593 | TTTATTGTGACACAC[A/G]TCACAAAGTATTGAT | 9886 |
rs780561332 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994089 | TAGAAATTATTGCTA[A/T]GTGTTAGGATAACAC | 9886 |
rs780572436 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970056 | TCAAAGACTGTATTT[C/G]CAGTGCACTCTCCAG | 9886 |
rs780574521 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916784 | GAATAGGGTTGCAGA[G/T]GGAATTAAGGTTGTT | 9886 |
rs780591022 | snp | A/G | 1.69375e-05 | 0.00291006 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893006 | CAGACCTAAAAGGAA[A/G]TCATAAAAGAAGCTT | 9886 |
rs780595676 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60939284 | CACACACACATCCAT[C/T]ATTTTTGGCGTCTTT | 9886 |
rs780598617 | snp | A/G | 1.66164e-05 | 0.00288235 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888522 | GACTTGCATTTCCCT[A/G]TGCATGCCAATGAAC | 9886 |
rs780609881 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60996083 | ACAGAAGTTGCTCAC[A/T]AGTCAAAGAACTCAT | 9886 |
rs780615998 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60963794 | CTTTCCAAATTACAA[G/T]TTCCCTGAAATATTT | 9886 |
rs780630550 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938901 | TTAACGTGTTTGGCA[C/T]CTAGTAGGGGCATAA | 9886 |
rs780661654 | snp | G/T | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60912060 | CAAAACTGTTATGGG[G/T]ACTTAGAGAATAATC | 9886 |
rs780669803 | in-del | -/ATCCATGA | | | intron-variant, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60872077 | CAGTCTCGAGGAATC[-/ATCCATGA]ATCCATGAGCTGCCT | 9886 |
rs780671388 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929011 | CATGTCTTCACATGG[C/T]AGCAGGAGAGAGATA | 9886 |
rs780682186 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940163 | ATATCCCTTTAAATG[C/T]TTAAAAAATATCTTC | 9886 |
rs780686986 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951036 | GACTACAAATACATA[C/T]ACAAACACCCTACTT | 9886 |
rs780690293 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949043 | GTTGGGCTCCAGCTA[A/G]TGATGACAAACAGGA | 9886 |
rs780699863 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60973350 | ATTTAGTTTATCTTT[C/T]TGTCTACATTCAAAA | 9886 |
rs780715172 | in-del | -/CC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916983 | AGGTAATGTATGTGA[-/CC]CACAGAAGCTAGAAG | 9886 |
rs780722615 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60940127 | CTTTTACAGGACAGA[C/T]GTGTTATAGGACAGC | 9886 |
rs780748352 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60911166 | TCATCTGTCTCAACC[C/T]TCATTCAGGATACCA | 9886 |
rs780757269 | in-del | -/G | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882834 | AACTTAGAGCTTTCC[-/G]GGGACAAATACCCTT | 9886 |
rs780805252 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60922561 | CCACGGGGAAAAGAA[C/T]TGGCCCAGGAAGTAG | 9886 |
rs780814877 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60873335 | GATGGGAGTATTTAT[A/G]TCATAGAAATTGGCA | 9886 |
rs780830869 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60885450 | GCTAGACCTAAGTAC[C/T]TTGAGAGGTGTGTTC | 9886 |
rs780846647 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951642 | CTCACATCCTGTCAC[C/G]GTATCCATCTTAGAA | 9886 |
rs780884233 | snp | C/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884828 | GATTACCAGAGGCTG[C/G]GATTAGGGGGTGAAT | 9886 |
rs780885043 | snp | C/G | | | intron-variant, upstream-variant-2KB | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60943580 | CGTATTCCCCTGTCC[C/G]GGTCCTCCGGTCCCC | 9886 |
rs780892406 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994342 | ATGTAATAGAAAGTG[A/C]GTGAGATTAGGTGGT | 9886 |
rs780924052 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60938942 | ATTGTTATCACAGCA[A/G]TCATTAGGAGTTTGG | 9886 |
rs780945432 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982332 | TGACAGTACTCAGTA[C/T]GGATACCATTTAGGT | 9886 |
rs780959681 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60889023 | GTGGGATTTCCAGAA[G/T]TGCAGGTGCCTGCGG | 9886 |
rs780986151 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985478 | TCATTTCTAAATCTT[C/T]CTTGTATATGGCCAT | 9886 |
rs780994737 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60982894 | CCCTCTTTCCTCTTC[C/T]GCTCCCTTCTTATGG | 9886 |
rs781014641 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60916383 | GCCAATCCTACAGCT[A/G]AATGTAGTTTATGAA | 9886 |
rs781038428 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60985610 | ATCAAAACTCATATG[C/T]AGGTCCAAATGACTC | 9886 |
rs781065977 | snp | A/G | 6.60458e-05 | 0.00574618 | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60886211 | ACTGATGGCTCCATC[A/G]TCCAATTTAAATGTC | 9886 |
rs781079337 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60904612 | GCTGAGGTTTGGTAA[C/T]GAGTATCAGAAAATT | 9886 |
rs781094205 | snp | C/G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994609 | TAGATTTTCTAATGT[C/G/T]AGGGAAAGATATCCT | 9886 |
rs781094450 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60962677 | AAAGCTTCTGTCCTT[C/T]GGTAAAGTCTTAAAA | 9886 |
rs781115776 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60898558 | GGCCGTGTAAGCTCA[C/T]ACTCATGGAGGATGG | 9886 |
rs781143645 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934737 | TATTATTCTCCCATG[C/T]TTACTGAAGTGAGGC | 9886 |
rs781156694 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60881796 | AAAGAAACTATTTCC[A/G]GCTGCAGCAGATGAC | 9886 |
rs781178596 | snp | C/G | | | synonymous-codon, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888945 | TGGAATTTTGATGAC[C/G]GGTGGAGGGGCTTTT | 9886 |
rs781182864 | snp | C/T | 4.9436e-05 | 0.00497148 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888842 | GTGCAAAGATGTGTT[C/T]CTGGTCCTGAAGGAT | 9886 |
rs781203691 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | RHOBTB1, LOC107984236 | GRCh38.p7 | 10:60945309 | AATAAACCTTTATTG[A/G]GTAGGCTGTGTGCAG | 9886 |
rs781238164 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60934317 | CTCATCAATATATCA[C/T]CTTGGAGTTCCTGGT | 9886 |
rs781267854 | snp | C/G | 0.000148438 | 0.00861376 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60877988 | AGATCCAAGTTAGGA[C/G]ACAACTGCTTGGTAT | 9886 |
rs781272487 | snp | C/G | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60888722 | GGAAATCTCTGCTCT[C/G]CTTCTCTTTCTCACA | 9886 |
rs781292903 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60933449 | TTCATTGGCTGGGTG[C/T]GGTGGCTCACGCCTG | 9886 |
rs781299436 | in-del | -/AG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924514 | TTATTAGAGCTAAAG[-/AG]AGAGAGAGAGAGAGA | 9886 |
rs781316712 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60949076 | GACTGACTGTTCTGA[G/T]GCTCTTCATTAATGC | 9886 |
rs781341091 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60900775 | TAAAGAATGAAAATA[C/T]AATGTGAGCCATTAC | 9886 |
rs781359141 | snp | A/G | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61003003 | GTTACATAGGTATAC[A/G]TGTGCCATGTTGGGT | 9886 |
rs781372777 | in-del | -/C | | | intron-variant, downstream-variant-500B | RHOBTB1 | GRCh38.p7 | 10:60882845 | TTCCGGGGACAAATA[-/C]CCTTAACCCCGTATG | 9886 |
rs781406050 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899290 | AAAGAAGGCTTGCTA[A/G]ACAGACGAAGGTGAA | 9886 |
rs781415315 | snp | A/G | 3.41962e-05 | 0.00413484 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60893016 | AGGAAATCATAAAAG[A/G]AGCTTGTATTGCCTT | 9886 |
rs781436613 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60979369 | AAACTTACCTAGTTA[A/C]AGTTTATCAATGGTC | 9886 |
rs781440368 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981522 | TTGCATTAACCAAGA[-/T]TTTTTCCCCCTTTAA | 9886 |
rs781462396 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906944 | ATGTCGTGGGAGGGA[C/T]CCAGTGGGAGGTAAC | 9886 |
rs781470407 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60929450 | TCAAAAACCCAAGTT[C/G]CCTTAAGGAAACTGC | 9886 |
rs781526893 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60892005 | TTCTCTCTCCTGCCG[C/T]CATACGAAGAAGGAT | 9886 |
rs781555974 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60994597 | TTTTAAAAAGTTAGA[-/T]TTTTCTAATGTGAGG | 9886 |
rs781565718 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60890883 | TTACCAACTGATGAA[A/C]CTCTTCAAGGCTTAG | 9886 |
rs781633332 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989677 | CTTTGCCCCTACTCT[G/T]GGTAGGTTTCCAACT | 9886 |
rs781681687 | in-del | -/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60941343 | TTCACCTCCCAGAGA[-/T]TTTTTTTTTTCTTTC | 9886 |
rs781682661 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60988249 | TGAAATACTCAACTT[C/T]TAACACACAGTTATA | 9886 |
rs781688788 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60906607 | TGCCTGTTTCTCCAA[C/T]CGTGAAATGAGCCTA | 9886 |
rs781693843 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886262 | GAAACACAACCATGA[A/G]CCAACTTTGCTGAGA | 9886 |
rs781699186 | snp | C/T | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60883073 | GAGAGTATATTATAG[C/T]TTACACAGGAAATAA | 9886 |
rs781715283 | in-del | -/CCAT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60981922 | TACAGGTGTGCACCA[-/CCAT]CCATGCCTGGCTAAT | 9886 |
rs781715704 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60919552 | ATCAAAACTTCACAG[A/C]ATTATATCTCCAGGA | 9886 |
rs781725680 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930487 | AGTGTGGAATAGTAA[C/T]GTGAAATACATTCGA | 9886 |
rs781738845 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958702 | ACTGCCTAGGAAGAG[A/G]TGATCCTCCTACCTG | 9886 |
rs781745544 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60918791 | CACTCTTGTTGCCAG[A/G]CTGGAGTGCAATAGC | 9886 |
rs781751592 | snp | C/T | 1.67987e-05 | 0.00289811 | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910867 | TCAAGCTCAACCACG[C/T]TGTACTAGTCTTGGT | 9886 |
rs796103597 | snp | A/C | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60958323 | TCATTTCTTTAGAAG[A/C]CCAAACTTCTGAGCC | 9886 |
rs796142598 | snp | A/G | | | intron-variant, utr-variant-3-prime | RHOBTB1 | GRCh38.p7 | 10:60884656 | TACTATATAGCCCTA[A/G]AAAAGAGGAAAATTC | 9886 |
rs796169201 | snp | A/G | | | missense, nc-transcript-variant | RHOBTB1 | GRCh38.p7 | 10:60892885 | TGGCACCCAACAAGG[A/G]TAACGGGTGTTCGAG | 9886 |
rs796179107 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60980319 | AAATCAATAAATGTC[C/T]GCTGGACCAATTGGT | 9886 |
rs796206645 | snp | C/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60924103 | TGGAAGACTCCAAAT[C/G]TGTGTATTTTTTTTC | 9886 |
rs796231897 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60969140 | AAATTGAAGTTGAGA[A/T]GGAACAAATTTAATG | 9886 |
rs796242884 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | RHOBTB1 | GRCh38.p7 | 10:61001079 | CGCGCGCGCGCACGC[-/GT]GTGTGTGTGTGTGTG | 9886 |
rs796249270 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60993934 | TCTTAATATTTGTAT[A/G]TACACTTTTAGAGCT | 9886 |
rs796269571 | in-del | -/GC | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886723 | AAGAGATGTGGGGGG[-/GC]GGGTGGGTCTGGCTA | 9886 |
rs796286242 | snp | A/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60951906 | TACTAAAAATACAAA[A/T]AATTAGCCGGGCATG | 9886 |
rs796298261 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60955047 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 9886 |
rs796304203 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60899639 | ATCCAGTATTATTCA[C/T]CAACCATCTAATCAT | 9886 |
rs796308683 | in-del | -/TA | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60895399 | AGTTAAAAATAAGAT[-/TA]TTTTTTATTTATTTA | 9886 |
rs796327063 | in-del | -/GGCCCCTGGGTCAGACTATG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60903661 | ACAGGCTGAGAAACA[-/GGCCCCTGGGTCAGACTATG]GGCCCCTGGGTCAGA | 9886 |
rs796486605 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60953819 | GTTTATAAATAGAAA[C/T]ACAAAGACACATGAA | 9886 |
rs796489349 | multinucleotide-polymorphism | GT/TG | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60886726 | AGATGTGGGGGGGGG[GT/TG]GGTCTGGCTATGTTG | 9886 |
rs796501984 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60930095 | GGAAATTAAGAAAAT[A/G]CTTTCTAATATATCC | 9886 |
rs796579181 | snp | G/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970082 | TCCAGTTGTATCTGG[G/T]CAGGGCATCATCCAA | 9886 |
rs796621830 | snp | A/G | | | intron-variant, upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:60913131 | AAGGATATATAGAAA[A/G]AATATTAAGAAGAAT | 9886 |
rs796731025 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60970941 | TCCCAGAATATATGC[A/G]TAACTCACCATTTTT | 9886 |
rs796733843 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60935779 | ATTTTCTGGTTATTT[C/T]TATTTACTATTAACT | 9886 |
rs796825418 | in-del | -/A | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60989203 | ATGAGAGAGAAAAAA[-/A]GTAGAAGTTGATGTG | 9886 |
rs796835822 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60948855 | CATATTTATACTGCT[C/T]ATGCTTATGGATTTT | 9886 |
rs796836910 | snp | C/T | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60910503 | TGGTCATGAAAAGAC[C/T]AAACAGTCTTTCTGA | 9886 |
rs796859283 | in-del | -/TT | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60879511 | TAATTTATTTTATTA[-/TT]ATTTTTTTTTTTTGT | 9886 |
rs796873647 | in-del | -/CTT | | | upstream-variant-2KB | RHOBTB1 | GRCh38.p7 | 10:61002931 | TTTCTTCTTCTTCTT[-/CTT]ATTATTATTATAATA | 9886 |
rs797001611 | snp | A/G | | | intron-variant | RHOBTB1 | GRCh38.p7 | 10:60992541 | GCTTCTAAAATTTAT[A/G]TCATCAAATGCAATA | 9886 |