SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs189839775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564987 | ATTAAGGAATAGGAT[C/T]GCAGCTGTCCCGCTC | 55213 |
rs189874227 | snp | A/G | 0.00235769 | 0.0342533 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534119 | ACCCAGCAGCCTTGC[A/G]CTTCAGTTCTTAAAG | 55213 |
rs189883922 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558679 | AGCCTGGGCAAGAAG[C/G]GTGAAACTCTGTCTC | 55213 |
rs189899848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570736 | GAAGAAACGAATAAC[C/T]ATCCTGAACCTGCCT | 55213 |
rs189910726 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549958 | GACACTGAGAAAATG[C/T]CCTAACAAATGTGAT | 55213 |
rs190124695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574615 | AATGAATTATTAATA[C/T]AAAATTAAATGTAGA | 55213 |
rs190142426 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537522 | AGATTCCTGGGCTCA[C/G/T]GTTTATCGCTTCCCT | 55213 |
rs190168287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576522 | AGTTCAGATTAGGGA[A/G]ATTCTCAACGGAGCA | 55213 |
rs190310593 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539120 | AGTGGCCCACCTTGG[C/T]CTCCCAAAGTGCCGG | 55213 |
rs190380648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553521 | TGAGAGGAGGCCCAT[C/T]TGCTGAAAGTAACAG | 55213 |
rs190417544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547018 | TTTAAGATATAAGAA[C/G]TGGGGGAAGCCTTTT | 55213 |
rs190469309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571411 | GCTTCTGCCTAGATT[C/T]GCCTGGTTAAACCTC | 55213 |
rs190557390 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586706 | TGTCCTGAATCACCA[C/T]CTCCCCCACTTAAAG | 55213 |
rs190622118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544065 | AGTTTTCTGCTTAAT[C/T]TATAATTAAAAGAGG | 55213 |
rs190665127 | snp | A/G | 4.96676e-05 | 0.00498311 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567199 | ACTGGCTGAGGTGCC[A/G]AAGACACACGCCTTC | 55213 |
rs190801299 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582419 | TTGAACTCGGGAGAC[A/G]GAGGTTGCAGTGAGC | 55213 |
rs190817283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561517 | CGGCAGGTGAAAGAA[A/C]TGTCCAAACTAATGA | 55213 |
rs190852459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581626 | AGGAGAGCAGAGTAC[C/T]TTAAGAAGAACTCTA | 55213 |
rs190863222 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587269 | GAATTTACTAGAAGA[A/G]GCCTGTTTTGCTCAA | 55213 |
rs190873250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539711 | GTCACAGGAAGGACA[A/G]GAAAAAAATCATACC | 55213 |
rs190880656 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544377 | AGGAGGCTGAGGCAG[C/G]AGAATCACTTAAACC | 55213 |
rs190918604 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538847 | CTCTAATTTTTCTAC[A/G]TTGAATCTGTAATAT | 55213 |
rs191119387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536455 | CTCTCTTTAGTATTA[C/T]AAGAATCTACATAAT | 55213 |
rs191152140 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559575 | GCAGGAAAATGGCGT[A/G]AACCCGGGAGGCGGA | 55213 |
rs191294135 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572560 | TAATCCCAGCACTTT[C/T]GGGAGGCTGAGGCAG | 55213 |
rs191357523 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552624 | CACAGTTTAACAGGC[A/G]AAATAGATACATGCA | 55213 |
rs191362147 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533758 | CCTGCTGTCAGAAGA[C/T]TGTTGATACGTGGCC | 55213 |
rs191385569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559837 | ATACACTTAAAACTG[G/T]TGAAGCTGGTAAATT | 55213 |
rs191415068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535690 | CTAAAAGATGCCCTA[A/G]AGTAAACTCCAGAAA | 55213 |
rs191642635 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535791 | GCACTTTGGGAGGCT[A/G]ATGCGGGCAGATCAC | 55213 |
rs191670693 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581996 | CACTCTGAAGGAAAA[A/G]TGAGAAATCGCATAG | 55213 |
rs191689523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577729 | TTTATTATGGAAGCC[A/G]ATAGCCAGAGGAAAC | 55213 |
rs191707752 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545822 | TTTTCCCTTGGTAGC[A/G/T]TGCTGTTACCAGAGC | 55213 |
rs191909553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563640 | CTCCAGCCTAGGCGA[C/T]AGAGCGAGACTGTCT | 55213 |
rs191923058 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542750 | TTCCTCTCTTCCCAG[A/G]CCTGCTACAAGCTTA | 55213 |
rs191931960 | snp | A/C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556821 | AAATATTAATATTCA[A/C/G]TATAATTATTCAAAG | 55213 |
rs191962445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548529 | TGACAGCACTACCCA[C/T]GAGAGTCAAAGGTGG | 55213 |
rs192235993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566967 | ATTATGAAACTCAGA[A/G]TGCTATGGAGTAGAC | 55213 |
rs192246384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546743 | TGAGAATCTAATACC[A/G]CTGCTGATCTGATGG | 55213 |
rs192272499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570523 | CCCAGGTTTGCTTTT[A/C]AAATCAGTCAGTATG | 55213 |
rs192404867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583312 | AGAAAGCTGGAGACC[A/G]TAAGTCTTTAGAGGT | 55213 |
rs192412857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583616 | CAGTGGCACAATCTC[C/G]GCTCACTGCAACCTC | 55213 |
rs192420035 | snp | C/T | 0.00219673 | 0.0330687 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540864 | CTGGTTTCTGTTTGT[C/T]GTTTAAGTTACCTCT | 55213 |
rs192464089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564569 | CAGCCTGGAGACAGA[A/G]CGAGACTCCTTCTCA | 55213 |
rs192659329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557927 | AATATGGTCATTAAA[A/G]TCAGAGGATTTTCAC | 55213 |
rs192670568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578283 | TAAATAGTTGTTAAC[A/G]TTTATTGCTTGGGGA | 55213 |
rs192670807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557615 | AGAGCATGGGACTCA[A/G]CTGCCTTAAAAAATG | 55213 |
rs192762155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563500 | AAACCCTGTCTCTAC[C/T]AAAAACACAAAAATT | 55213 |
rs192825022 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531568 | GAACTCAGGCAGTAA[C/T]GCTCACTCATCCGCC | 55213 |
rs192863852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537012 | CATTGATGGTCTTAA[C/T]ATCCTCATTTTAAAA | 55213 |
rs192881264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578975 | ATTACAACTTAATGT[C/G]TTCCATCTATGCTAC | 55213 |
rs192988735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583471 | CATTAACTGATCTCC[C/T]CTACTAAGTCTATTC | 55213 |
rs193029073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550588 | CAAGAGCAGATTTAT[C/T]TAAAAGTTGTTTTAC | 55213 |
rs193054544 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551861 | GCTGAGATCGTGCCA[C/T]TGCACTCCAGCCTGG | 55213 |
rs193151665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568572 | ACAGCGTACTCTCAC[A/G]GCATTTCAGTTTTGT | 55213 |
rs193232071 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532891 | AAAAGCAAGCTCAAC[A/G]GACACACATGATGAA | 55213 |
rs193240873 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572157 | CATGGTGAAACCCTG[A/C]CTCTACAAAAAATAC | 55213 |
rs193292487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547106 | CAGCTGGGTATGCCA[C/T]ACATGTGCAATTCTG | 55213 |
rs199503999 | snp | C/T | 0.000447031 | 0.0149437 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559911 | AGAATAAAAGCAGCA[C/T]ACTTACCTCTCCATC | 55213 |
rs199507818 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572151 | AGATGACATGGTGAA[A/C]CCCTGCCTCTACAAA | 55213 |
rs199527104 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533085 | AAAAGTGAAAGATGA[A/T]AAAGTTTCACATAAG | 55213 |
rs199588684 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533078 | GAAAACCAAAAGTGA[A/C]AGATGATAAAGTTTC | 55213 |
rs199613344 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577533 | CTAGTTTAAATTGCT[-/G]TTATGTACTGGCTTT | 55213 |
rs199667765 | snp | A/T | 0.000416601 | 0.0144266 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534088 | CCTCAACAGTGCCCC[A/T]GAGCACTCACACAGA | 55213 |
rs199724988 | in-del | -/C/CT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538887 | TTAAGTTTTTTTTAA[-/C/CT]CTTTTTTTTTTTTTT | 55213 |
rs199728094 | in-del | -/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585168 | GCACCTCAAAAAAGA[-/TT]GAGGGAGGCAGGGAA | 55213 |
rs199774257 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551692 | GATCACAAGGTCAGG[A/G]GATTGAGACCATCCT | 55213 |
rs199782704 | snp | C/G | 6.60415e-05 | 0.00574599 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549499 | GCGGGAGTGGCAAAG[C/G]AGGCAAACACGTCGT | 55213 |
rs199788678 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533082 | ACCAAAAGTGAAAGA[A/T]GATAAAGTTTCACAT | 55213 |
rs199810507 | in-del | -/A | 0.0109229 | 0.0730898 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559878 | GATGAAAAAAAAAAA[-/A]GAATAAAGAATAAAA | 55213 |
rs199818649 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562101 | GGACTCTATCTCAAA[A/G]AAAAAAAAAAAAAGG | 55213 |
rs199823176 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566286 | AAAATAAATAAATAA[A/T]TAAATAAATAAATAA | 55213 |
rs199916443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541030 | AAAATATGTGAAAGG[C/T]TTAATCAAATGTATA | 55213 |
rs200110498 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555181 | TGTACAGTTGACATT[-/G]TTTCATTGGAAGAGA | 55213 |
rs200166799 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535058 | AAAAAATTCACCTTA[A/C]ATTCACTTTTATGCT | 55213 |
rs200175783 | in-del | -/T | 0.0329836 | 0.124112 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574040 | CCACCCACCTGGGCC[-/T]CCCAAAGTGCTGGGA | 55213 |
rs200201778 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583386 | AGTGTGCTTTTGTGT[A/G]TGTGTGTGTGTGTGT | 55213 |
rs200243704 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544892 | ACATATATTAATATG[A/G]CAAGTTCAAGGAACA | 55213 |
rs200403352 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533076 | AGGAAAACCAAAAGT[G/T]AAAGATGATAAAGTT | 55213 |
rs200432773 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558718 | AAAAAAAAAAAAAAA[-/T]TCACAAAGTAGACAA | 55213 |
rs200435946 | snp | G/T | 1.67539e-05 | 0.00289425 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549634 | GCAGAGTGACAGGCT[G/T]CAATCTCTACCACCC | 55213 |
rs200635053 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538774 | ACACACACACACACA[C/T]ATATATATATGCCCT | 55213 |
rs200694108 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533083 | CCAAAAGTGAAAGAT[C/G]ATAAAGTTTCACATA | 55213 |
rs200696623 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533080 | AAACCAAAAGTGAAA[A/G]ATGATAAAGTTTCAC | 55213 |
rs200753466 | in-del | -/GGGGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568650 | AAAATAATCAGGCCG[-/GGGGA]GGGGGGTGGCTCACA | 55213 |
rs200761846 | snp | A/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586740 | ACCAGGGCCAATGAT[A/T]AAAAAAAAAAAAAAA | 55213 |
rs200806564 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562473 | TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC | 55213 |
rs200809575 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566287 | AAATAAATAAATAAA[A/T]AAATAAATAAATAAA | 55213 |
rs200826424 | snp | A/G | 0.000181478 | 0.00952397 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549530 | CGGTGCAGGAGAAGT[A/G]GGTGAGGTGCGGGAG | 55213 |
rs200832316 | in-del | -/AAAA | 0.119674 | 0.213343 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564891 | GAGAGACTCCGTCTC[-/AAAA]AAAAAAAGAAAGAAA | 55213 |
rs200873191 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551900 | GGGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 55213 |
rs200891767 | snp | A/G/T | 3.44952e-05 | 0.00415288 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541010 | AATCCAGAAGACCTA[A/G/T]AAGTAAAATATGTGA | 55213 |
rs200902196 | snp | C/T | 0.00130362 | 0.0254973 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534118 | AACCCAGCAGCCTTG[C/T]GCTTCAGTTCTTAAA | 55213 |
rs200928511 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574684 | AGATGGTGATTCCTT[-/A]AAAAAAAAAAAAAAA | 55213 |
rs200997017 | snp | A/G | 0.00129666 | 0.0254292 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551289 | CCCCAAGGCCACATC[A/G]CACACACAGTCCCAA | 55213 |
rs201057287 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547174 | ATCACAATACTCACT[A/G]CAAAAAAAAAAAAAT | 55213 |
rs201058461 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533084 | CAAAAGTGAAAGATG[A/C]TAAAGTTTCACATAA | 55213 |
rs201154849 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533077 | GGAAAACCAAAAGTG[A/T]AAGATGATAAAGTTT | 55213 |
rs201207676 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543702 | CTATATCTTAAAAAC[-/T]TTTTTTTTTCATTTT | 55213 |
rs201220063 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560000 | AAGAGATTGGTACAG[A/G]CCTGGACGGGAGCAA | 55213 |
rs201265040 | in-del | -/AC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574935 | CTGATACATACAACA[-/AC]AGGGATGAACCCTGA | 55213 |
rs201278992 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567172 | ATCATTGTCAGTAAC[A/G]TACAGTGCTTCACTG | 55213 |
rs201341255 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569794 | TGCCTGCAGTCTCAG[C/T]TACTCAGGAGGCTGA | 55213 |
rs201363899 | snp | A/T | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569429 | AAATACAAAAAAAAA[A/T]GGCCAGGCACGGTAG | 55213 |
rs201384276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568652 | AATAATCAGGCCGGG[G/T]GAGGGGGGTGGCTCA | 55213 |
rs201410994 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538903 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 55213 |
rs201415093 | snp | A/G | 0.00299552 | 0.0385848 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552220 | TGCCACTCTCACAGG[A/G]GTCAGCTGGTTGCCA | 55213 |
rs201650393 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566283 | AATAAAATAAATAAA[A/T]AAATAAATAAATAAA | 55213 |
rs201662457 | snp | A/G | 3.45572e-05 | 0.00415661 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541644 | TATATTCTCCACCAT[A/G]CGGCTCGTCCATCCC | 55213 |
rs201666361 | snp | A/C | 3.38713e-05 | 0.00411516 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567110 | TTTGAAGACCAATTG[A/C]CAAATAAGTCCTAAA | 55213 |
rs201677080 | in-del | -/AG | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532181 | GTAGAAAAATAAGAG[-/AG]TGTATTTAAAAAAAA | 55213 |
rs201826156 | in-del | -/AAAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544474 | AACTCTGTCTCAAAG[-/AAAC]AAACAAACAAACAAA | 55213 |
rs201873611 | in-del | -/AT | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575657 | AAAACCAAATACCAC[-/AT]GTTGTCACTTAGAAA | 55213 |
rs201964285 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559983 | CCACCACTTGCTTGA[G/T]CAAGAGATTGGTACA | 55213 |
rs202022853 | in-del | -/AAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574698 | TTAAAAAAAAAAAAA[-/AAC]ATTAGAATTATATTA | 55213 |
rs202071748 | snp | C/T | 0.000205314 | 0.0101299 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549660 | CACCCTGAAAAGTTT[C/T]AAGAAAAATGCATGT | 55213 |
rs202073736 | snp | A/C | 0.00199795 | 0.0315433 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534180 | TCCTTTAGCAGAGGG[A/C]CATCCATTTGCCAAA | 55213 |
rs202093085 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551151 | GAAGGGGGAAGGGGG[-/A]AGCAGGGAGGGAGAA | 55213 |
rs202101078 | snp | C/T | 5.14708e-05 | 0.00507274 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541652 | CCACCATGCGGCTCG[C/T]CCATCCCAATGCTAC | 55213 |
rs202120148 | in-del | -/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544967 | GGATAATTCCACTTG[-/T]TTTTTTTTTCAAGAG | 55213 |
rs202123073 | snp | A/G | 1.68992e-05 | 0.00290677 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567116 | GACCAATTGCCAAAT[A/G]AGTCCTAAAACGAAA | 55213 |
rs202123523 | snp | A/G | 0.00199792 | 0.0315431 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567194 | GCTTCACTGGCTGAG[A/G]TGCCGAAGACACACG | 55213 |
rs202152541 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569814 | CAGGAGGCTGAGGTG[A/G]GAGGATTGCTTGAAC | 55213 |
rs202230217 | in-del | -/A | 0.43221 | 0.171171 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562773 | CGTGCCACCATCCCC[-/A]GGCTTTTTTTTTTTT | 55213 |
rs367598034 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573448 | GATACAATTCCTCAT[C/T]TTTTTTTTTTTTTTT | 55213 |
rs367646872 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569867 | GAGCCGAGATCACAA[C/T]GCTGCACTCTAACCT | 55213 |
rs367651925 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551769 | GCCAGGTGTGGTGGC[A/G]GCCATCTGTAGTCCC | 55213 |
rs367749129 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579275 | TATGTTATTGCCCCA[A/G]CTGCTAGAACAGCTG | 55213 |
rs367755809 | snp | C/T | 0.000932121 | 0.0215683 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544910 | AGTTCAAGGAACAGA[C/T]TGAAGATTCAAAAGA | 55213 |
rs367871553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560958 | CCCCTCCCAGCACCT[C/T]GATGTGGTCACCAAC | 55213 |
rs367889455 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538267 | CTGAGTAGCTAGAAT[A/G]CAGGCATGAGCCACT | 55213 |
rs367914694 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576119 | ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 55213 |
rs367975060 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584028 | CCTCACTTTCCTTCA[C/G]AGTTTCATCTACCCC | 55213 |
rs368011355 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567067 | CTTTATTTATACCCC[A/G]CCTTTTCTCCATCTT | 55213 |
rs368132465 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549438 | TCTTCCTGGGTGGAG[A/G]TGGCCCTGCACTTTC | 55213 |
rs368158256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582899 | AGTGGAGTGGAGGCC[A/G]GGTGTGGTTGCTCAC | 55213 |
rs368202795 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554111 | GGATGCTATACAGGG[C/G]AGCGGGAAGCAGGCT | 55213 |
rs368217569 | snp | C/T | 4.95577e-05 | 0.00497759 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549584 | GGCCCCACATGTACA[C/T]GTGCCCACCCTGCGT | 55213 |
rs368286861 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552991 | GATCGAGACCATCCT[G/T]GCCAACACAGTGAAA | 55213 |
rs368296279 | snp | A/C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548648 | AATGAAATACAGAGA[A/C/T]ATATTACGTCAATGG | 55213 |
rs368344889 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583000 | TGGGCAACATAGGGA[A/G]ACCCTGTCTCTACAA | 55213 |
rs368350410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564948 | ACCCTGAAAGTTGCA[C/T]TGCAGAACAAAGACC | 55213 |
rs368445009 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539543 | CCTGAGTATGGAACT[A/C]GTTAACAAGGAGGAG | 55213 |
rs368460197 | in-del | -/AGGG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568654 | TAATCAGGCCGGGGG[-/AGGG]GGGTGGCTCACACCT | 55213 |
rs368475555 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563734 | AAGTGAGATAATCAC[C/T]TCATTATGCTCAACT | 55213 |
rs368518581 | snp | A/C | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581995 | TCACTCTGAAGGAAA[A/C]ATGAGAAATCGCATA | 55213 |
rs368531856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558643 | AGGTTGCAGTGGGCC[A/G]AGATTGTACCATTGC | 55213 |
rs368537401 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573191 | AGCTATGTTATAAAA[C/T]AATATGTCCTGTATG | 55213 |
rs368583726 | snp | A/G | 3.32668e-05 | 0.00407827 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567252 | GGGAGAGTAGAGTGA[A/G]GATGGGCCACTTTCC | 55213 |
rs368761579 | snp | G/T | 1.68088e-05 | 0.00289899 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566578 | GAATTAACCGGTCAA[G/T]TTCTTACAAACTGAA | 55213 |
rs368791716 | snp | A/T | 3.40333e-05 | 0.00412498 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555649 | ATCCCACTTGGCCAC[A/T]GTTGTTATAACCCCA | 55213 |
rs368791916 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578350 | AAATGCAATTTTTAA[C/T]ATTTGCAATTTGAGG | 55213 |
rs368795245 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556262 | AGTGCAGTGGTGCGA[C/T]CTCAGCTCACTGCCA | 55213 |
rs368828141 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573769 | TTGTATTTTTAAAAT[A/G]TAGTCCCAAATTTCT | 55213 |
rs368866477 | snp | A/G | 6.59359e-05 | 0.00574139 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541761 | GTAAGAAAACTGATC[A/G]ATTTCTATCACTTCC | 55213 |
rs368875643 | in-del | -/T | 0.472052 | 0.11486 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573449 | ATACAATTCCTCATC[-/T]TTTTTTTTTTTTTTT | 55213 |
rs369014593 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561485 | AAGTATGATCCATGA[C/T]ATTGTGTTAAAAGCT | 55213 |
rs369057732 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546808 | GAGCAGCTGTAAATA[C/T]AGATGAAGCTTCGCT | 55213 |
rs369148915 | in-del | -/A/AA/AAAA | 0.499891 | 0.00738737 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559655 | GCGAGACTCCATCTC[-/A/AA/AAAA]AAAAAAAAAAAAAAA | 55213 |
rs369157844 | snp | A/G | 8.91417e-05 | 0.00667554 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566807 | CTGAGTCTTTTGACC[A/G]AAAGCTGTATTAAAA | 55213 |
rs369203281 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571329 | CCAGCCTGGGGAAGA[A/G]GAGCGAAACCCCATC | 55213 |
rs369287917 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570089 | TTATGAACCATATCA[A/G]GTTAGCCTTCAAAAT | 55213 |
rs369317460 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565867 | ATCAGATTGTTGCTG[C/T]GTCTGTGTAGAAAGA | 55213 |
rs369333333 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550923 | CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 55213 |
rs369340030 | snp | A/G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568939 | TCTCGAAAATAAAAA[A/G/T]TAATGATCAGAATAA | 55213 |
rs369380225 | snp | A/G | 1.6498e-05 | 0.00287206 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560067 | ATCCATTGTGGCCCC[A/G]GGCATAAACCACTCC | 55213 |
rs369408500 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534161 | ACTGGCTTTAGCAAT[C/G]AATTCCTTTAGCAGA | 55213 |
rs369494601 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551513 | GCAGGAAAACAGGAA[C/G]GGCAGGGAGAACATC | 55213 |
rs369643088 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564276 | AAGAAAGGAAAGCCA[A/G]GTAGCATCTATGTTT | 55213 |
rs369656790 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542772 | ACAAGCTTATTTATA[A/T]AACACTCACATCCAC | 55213 |
rs369713862 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541830 | AAAATGCTCACACCT[A/G]AAACAGCAAAGCAAA | 55213 |
rs369748688 | in-del | -/T/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573448 | ATACAATTCCTCATC[-/T/TT]TTTTTTTTTTTTTTT | 55213 |
rs369801806 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553379 | TTTCTTCCCTCGTTA[A/G]CAAATAGGTGAGCTC | 55213 |
rs369848049 | snp | A/G | 0.000214452 | 0.0103528 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540948 | TCCTCTCTTGATAAT[A/G]TGCTGACAAAGTTTT | 55213 |
rs369966770 | snp | A/C | 0.000151613 | 0.00870539 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566569 | CTAAGCTTAGAATTA[A/C]CCGGTCAATTTCTTA | 55213 |
rs370058321 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579707 | ATGTAGCCTTCTCCC[A/G]AAGTAGTTTGTCATC | 55213 |
rs370173763 | snp | A/G | 0.000231539 | 0.0107571 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566622 | TCCCTCCTTACCTTC[A/G]GTGCTGAGAAGAACA | 55213 |
rs370245798 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548207 | CCAGCCTGATCAACA[C/T]TGTGAAACTCTGTCT | 55213 |
rs370261369 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566409 | GCAGTCGAAAACCTC[A/T]GAAGTTTGCCTAATT | 55213 |
rs370298189 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574812 | AAGCAGCATTATTCA[C/T]AATAGCCAAAATGTG | 55213 |
rs370304772 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572344 | AAAAAAAAAAAAAAA[G/T]GCAGGATCCATTGCA | 55213 |
rs370331873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562918 | GCATGAGCCACCACA[C/T]ACAGCCAACAAGGGA | 55213 |
rs370379921 | snp | C/T | 1.69198e-05 | 0.00290854 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544718 | AGTTATTGATGTCTC[C/T]GAGCTCATGCAAAAA | 55213 |
rs370565779 | snp | C/T | 0.000121096 | 0.00778031 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541645 | ATATTCTCCACCATG[C/T]GGCTCGTCCATCCCA | 55213 |
rs370587867 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555406 | TTTCAATGGAGCTAC[C/G]AAAACAAAGCACTCT | 55213 |
rs370652161 | snp | C/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555603 | CAGTTTGTAACTTTT[C/T]GAGGAGTTGGTTGAT | 55213 |
rs370658550 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571051 | TAAACTGTTACCAAT[A/G]TAAAAAGTATCCAGG | 55213 |
rs370699299 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544501 | AAACAAACAAACAAA[A/C/T]ACAAAAAACCAATAT | 55213 |
rs370735633 | snp | C/T | 3.3849e-05 | 0.0041138 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566781 | GACCTAGAAAATAGA[C/T]AGTTTTTTTTCTGAG | 55213 |
rs370772744 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544921 | CAGATTGAAGATTCA[A/G]AAGACTTCAAAAAGA | 55213 |
rs370777592 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544126 | TATTTTCTTTAACCA[C/T]GTAAATAAATTTTCT | 55213 |
rs371060996 | snp | A/G/T | 0.000131796 | 0.00811686 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560030 | ATGCCTTGGTTGGTC[A/G/T]TCCCATTCCCAAGCT | 55213 |
rs371102887 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548715 | GGGTCACATATTGTA[C/T]GCTTCCGCTTATATG | 55213 |
rs371147347 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582084 | CATTGTTAGAGGCTT[A/G]AACATGTTTGAATTA | 55213 |
rs371171861 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534054 | ATCACATCACCCGTA[A/G]AGCACAAACTGGACA | 55213 |
rs371265725 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553168 | GCCTGGCAACAACAA[A/C]AACAAAAAGACTAGA | 55213 |
rs371439745 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548899 | TGTAGGCCAGGCACA[A/G]TGGCAGGTGGATCAC | 55213 |
rs371454809 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563774 | TTCATACCACATGAT[A/G]ATGCTCAGATTTGGA | 55213 |
rs371558865 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564474 | GTCTGTGGTCTCAGC[G/T]ACTCGGGAGGTTGAG | 55213 |
rs371583314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562276 | TGACATAAGCGTTGT[A/T]AGATAAAGTTGAAGA | 55213 |
rs371629396 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583158 | CCAGACTGGGCGACA[A/C/T]AGTGAGACCCTGTCT | 55213 |
rs371654556 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576449 | GAAAGGTTTCAGTCC[C/T]AAAAAATGTGTTTGG | 55213 |
rs371662007 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561751 | AATAAATAGGAAAAC[C/G]CTACAAAAAAAAAAG | 55213 |
rs371693104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565811 | GACGATGGCGGTTTC[A/G]TCGAATAGAAAAGGG | 55213 |
rs371821814 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534791 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 55213 |
rs371941819 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568662 | CCGGGGGAGGGGGGT[C/G]GCTCACACCTGTAAT | 55213 |
rs371981479 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568219 | CTATATTAGCACACA[C/T]AGACCTGCTACATTT | 55213 |
rs372016733 | snp | A/G | 1.66977e-05 | 0.00288939 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549483 | GAGGCGCCACGAGAC[A/G]GCGGGAGTGGCAAAG | 55213 |
rs372029476 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535198 | AGTTTTCAGTCAAAC[A/G]GAAGTCACCAACTAC | 55213 |
rs372094611 | snp | A/G | 8.28768e-05 | 0.00643673 | stop-gained, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555604 | AGTTTGTAACTTTTC[A/G]AGGAGTTGGTTGATT | 55213 |
rs372107028 | snp | C/T | 1.65173e-05 | 0.00287374 | missense, synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559920 | GCAGCATACTTACCT[C/T]TCCATCAGCTGCCAG | 55213 |
rs372115553 | snp | A/G | 0.000355351 | 0.0133248 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534304 | AAAATGGCTTTTTTA[A/G]GCAACTTTGATTGAA | 55213 |
rs372161323 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578627 | GTCCATGTGACACAT[A/G]TTAATATGTCAAATA | 55213 |
rs372162764 | snp | C/G/T | 3.29469e-05 | 0.00405864 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560019 | GGACGGGAGCAATGC[C/G/T]TTGGTTGGTCGTCCC | 55213 |
rs372173951 | snp | A/C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565778 | GTACCCAACAGCTCA[A/C/T]TGAGAACAGGCCATG | 55213 |
rs372180903 | multinucleotide-polymorphism | CC/GG | 0.0139853 | 0.0824443 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557254 | TCAACTTAAAAGATA[CC/GG]GAATAGAAGGGACTA | 55213 |
rs372206202 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556353 | CCGCCACCATGCCCG[G/T]CTAATTTTTTGTATT | 55213 |
rs372239944 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548263 | CAGGCATGGTGGCAC[A/G]CGCCTGTAATCCCAG | 55213 |
rs372251050 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587231 | TGAATGAAGTGGCTT[G/T]CCCAAAGTAGTGGCA | 55213 |
rs372290207 | snp | A/C/G | 4.98139e-05 | 0.00499048 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567160 | GACTCTTACCTCATC[A/C/G]TTGTCAGTAACGTAC | 55213 |
rs372373318 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574235 | GCAATTCTTGTGCCT[A/C]AGCCTTCTGAGTGGC | 55213 |
rs372400658 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49531980 | GTTTATTAACATGTC[A/G]TTCTAAATATTACAT | 55213 |
rs372411448 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570190 | TAAGACATTCAAAAC[C/T]ACACAACTTCCTGAC | 55213 |
rs372422690 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552873 | GGCTGGACACAACTG[C/T]GGTAGTGGTAGTAGA | 55213 |
rs372488157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581213 | CGACAAAGGAGTGCT[C/T]AGAGGAAGTCCAGAT | 55213 |
rs372696013 | snp | C/T | 5.02601e-05 | 0.00501274 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551307 | CACACAGTCCCAAGA[C/T]GTGGCACAGCCAAGT | 55213 |
rs372745616 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570516 | CCTGTGTCCCAGGTT[G/T]GCTTTTAAAATCAGT | 55213 |
rs372762429 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536805 | TAAAGTGTTCTAAGG[C/T]AAATGAGATAAAATA | 55213 |
rs372793586 | snp | C/G | 3.41658e-05 | 0.00413301 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551519 | AAACAGGAAGGGCAG[C/G]GAGAACATCTACTTA | 55213 |
rs372802348 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564215 | AACTACATGAATGCC[A/G]GAGAACAGATGAAGA | 55213 |
rs372804080 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542530 | TTCAGAAACAAGAGT[A/T]CAAAACTTTTGACTA | 55213 |
rs372827262 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542307 | CAAAAAACATTCCAC[A/G]TGCAAGTGGTTTTTG | 55213 |
rs372857521 | snp | C/T | 3.30475e-05 | 0.00406481 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549586 | CCCCACATGTACACG[C/T]GCCCACCCTGCGTCT | 55213 |
rs372881742 | snp | C/T | 0.00018908 | 0.00972132 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544686 | CATTTTGTGGAATAA[C/T]AAAGAAAGAAAAGTC | 55213 |
rs373039398 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551983 | TTTTTTTTAACTTGT[C/T]GAGCCTGTTTTGCCA | 55213 |
rs373186397 | in-del | -/AAATAAATAAATAAAT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566272 | TAAAAAAATAAAATA[-/AAATAAATAAATAAAT]AAATAAATAAATAAA | 55213 |
rs373262951 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586929 | TTCCTACTCATCTTT[C/G]AAAATCCAGGTCAAA | 55213 |
rs373268909 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560106 | ACACAAAGCACACAA[A/G]AAATCAGCTCCAAAA | 55213 |
rs373270376 | snp | A/G | 3.31164e-05 | 0.00406904 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544769 | TTTATGGACATGAAT[A/G]TATTTTCCATCAATT | 55213 |
rs373274582 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571334 | CTGGGGAAGAAGAGC[A/G]AAACCCCATCTCAAA | 55213 |
rs373300707 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558147 | GGTTTTCTCTGGGTA[C/G/T]TCTGATTTCCTCCCA | 55213 |
rs373324143 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570879 | CAAAGGTGAAATGAC[A/G]CCAAGGTCACACAGC | 55213 |
rs373326767 | snp | A/G | 0.00028158 | 0.0118622 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567184 | AACGTACAGTGCTTC[A/G]CTGGCTGAGGTGCCG | 55213 |
rs373425054 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555190 | GACATTGTTTCATTG[C/G]AAGAGAAAGGTAGGA | 55213 |
rs373469529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543220 | AGTGAGCTGGTATTA[C/T]GCCACTGCACTCTAG | 55213 |
rs373602247 | snp | A/G | 3.37223e-05 | 0.00410609 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555464 | TGTGAAGAAACTGAC[A/G]TGTAATTGAAAAAGA | 55213 |
rs373711625 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568663 | CGGGGGAGGGGGGTG[A/G]CTCACACCTGTAATC | 55213 |
rs373888606 | snp | C/G/T | 5.16225e-05 | 0.00508026 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541650 | CTCCACCATGCGGCT[C/G/T]GTCCATCCCAATGCT | 55213 |
rs373942056 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545925 | CATCAGACTCTCCCC[C/G]AAGGCATTACCTTTC | 55213 |
rs373995973 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540062 | CTAGATATTTTGAAA[A/C]TCCAAGGCTATTGCT | 55213 |
rs374040451 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544259 | CAGATCACCTGAGAT[C/T]GGGAGTTCGAGACCA | 55213 |
rs374048247 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558426 | GCTTGTCATGGTGGC[-/T]TATGCCTGTATTCCC | 55213 |
rs374052145 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565289 | CCCGAGGTGCCGAGA[C/T]TGCAGACGGAGTCTC | 55213 |
rs374104747 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544502 | AACAAACAAACAAAC[A/C]CAAAAAACCAATATG | 55213 |
rs374135653 | snp | A/C/T | 0.000115308 | 0.00759222 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560007 | TGGTACAGACCTGGA[A/C/T]GGGAGCAATGCCTTG | 55213 |
rs374141535 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563243 | ATCTCTACAAAAAAA[-/A]TTTAAAAATGAGGTG | 55213 |
rs374145103 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545185 | ACCCCCTCTCAAAAC[A/G]AGTGGTTCTCTTCTA | 55213 |
rs374283892 | snp | A/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566671 | CTGAGGCTTTTAATC[A/T]TCTTTCCACATAAGC | 55213 |
rs374300740 | snp | A/C/T | 0.000438699 | 0.0148043 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567127 | AAATAAGTCCTAAAA[A/C/T]GAAACTAGGTTTCAA | 55213 |
rs374303116 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566572 | AGCTTAGAATTAACC[A/G]GTCAATTTCTTACAA | 55213 |
rs374399241 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548551 | CAAAGGTGGGAACAA[C/T]CCACATGTCCATCAA | 55213 |
rs374407048 | snp | A/G | | | intron-variant, missense | RCBTB1 | GRCh38.p7 | 13:49558311 | GCGCTGCCAGAAGAG[A/G]CTGTGGCCACATGCA | 55213 |
rs374463381 | snp | A/G | 4.98832e-05 | 0.00499391 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567242 | ATCTCTTGAGGGGAG[A/G]GTAGAGTGAAGATGG | 55213 |
rs374537790 | snp | C/G | 3.29745e-05 | 0.00406031 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540889 | ACCTCTGCATCATAT[C/G]TGACTGCAGCAGAGA | 55213 |
rs374578940 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581991 | AATTTCACTCTGAAG[A/G]AAAAATGAGAAATCG | 55213 |
rs374664515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562441 | CAGGTGTGAACCACC[A/T]GCTCACACAGTGAGG | 55213 |
rs374719087 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564164 | AAAAAAGGACAAGAA[C/T]CTATCAACCTGCATC | 55213 |
rs374729539 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533332 | AGTTCTCAAGTTCTA[A/C]CTTAATGAAATAAAA | 55213 |
rs374736816 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573535 | CTCACTGCAATCTCC[A/G]CCTCCTGGGTTCAAG | 55213 |
rs374759756 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571661 | AGGTTTTGTGGGGCT[A/G]TGTGCCAGGCAGAAC | 55213 |
rs374782051 | snp | C/G | 1.79024e-05 | 0.0029918 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549420 | GTCAGTTGGTAGTAC[C/G]ATTCTTCCTGGGTGG | 55213 |
rs374794490 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565786 | CAGCTCATTGAGAAC[A/G]GGCCATGATGACGAT | 55213 |
rs374913321 | in-del | -/AGG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568654 | TAATCAGGCCGGGGG[-/AGG]GGGGTGGCTCACACC | 55213 |
rs374924752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542139 | GAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGT | 55213 |
rs374958508 | snp | G/T | 6.59304e-05 | 0.00574116 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541743 | AAAGGCACGATACAC[G/T]GGGTAAGAAAACTGA | 55213 |
rs374987776 | in-del | -/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559073 | ATAGGAACTTAACTC[-/TT]GTTTTTATCAATTAG | 55213 |
rs375046839 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531581 | AATGCTCACTCATCC[A/G]CCACTCACCTCCCGC | 55213 |
rs375090778 | snp | A/T | 1.67967e-05 | 0.00289794 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555634 | TTGCTGTAGAACCTG[A/T]TCCCACTTGGCCACA | 55213 |
rs375178683 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536241 | AAAACAATCTAAATC[C/T]GGGTTGTGTAAGTAA | 55213 |
rs375288062 | snp | G/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586870 | CCACTTCAACTACTG[G/T]TTGGCTCTGGTTTTC | 55213 |
rs375322776 | snp | A/G | 3.33946e-05 | 0.00408609 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540991 | TCACAGTAAGATGTC[A/G]CCAAATCCAGAAGAC | 55213 |
rs375337251 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538200 | AGTCTCACTATGTTG[C/T]CCAGGCTGGTCTCAA | 55213 |
rs375367070 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560034 | CTTGGTTGGTCGTCC[C/T]ATTCCCAAGCTGGCT | 55213 |
rs375379904 | in-del | -/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551959 | TACTGAATTTTTCCA[-/TT]TTTTTTTTTTTTTTT | 55213 |
rs375437747 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544495 | ACAAACAAACAAACA[A/C]ACAAACACAAAAAAC | 55213 |
rs375444241 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533155 | ATTCCACTAAGTCTT[A/G]TAAGAGGGTTGACTT | 55213 |
rs375524474 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576735 | GATAGTAATTTTTTT[-/T]GCAAGCCTTCCATGT | 55213 |
rs375540798 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586962 | CCGCCTACTCTTGTC[C/T]TCCCAGCATCCTCTT | 55213 |
rs375670496 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550594 | CAGATTTATTTAAAA[C/G]TTGTTTTACTTGGCT | 55213 |
rs375806894 | in-del | CTG/TTTT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551959 | TACTGAATTTTTCCA[CTG/TTTT]TTTTTTTTTTTTTAA | 55213 |
rs375837546 | snp | C/T | 0.000116638 | 0.00763581 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567313 | TTCCTATAAATAAGC[C/T]GACATCTCTGCTGGA | 55213 |
rs375845675 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574123 | CCCAAATTTCTTTTT[C/T]TGGGGGTGGGGGGTG | 55213 |
rs375887697 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551052 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC | 55213 |
rs375894962 | snp | A/T | 0.00303658 | 0.0388467 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559867 | TTTATGTTAAGTGTA[A/T]TTACTATGATGAAAA | 55213 |
rs375976880 | in-del | -/CAGT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558765 | TAACAATAAACAACA[-/CAGT]CAAACACCCTCAGTG | 55213 |
rs376000101 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533738 | ATTCCCCAACTATCA[C/T]TGCTCCTGCTGTCAG | 55213 |
rs376030531 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564268 | AATGCACAAAGAAAG[C/G]AAAGCCAGGTAGCAT | 55213 |
rs376059348 | snp | C/T | 5.12545e-05 | 0.00506207 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544700 | ACAAAGAAAGAAAAG[C/T]CAAGTTATTGATGTC | 55213 |
rs376102137 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584905 | ACAAGGGAAACGTCA[C/G]TTATTTAGAGTTCAC | 55213 |
rs376136462 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579481 | ACAAAAAAATTAGCC[A/G]GGCCTGGTAGTGGGC | 55213 |
rs376145738 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559581 | AAATGGCGTAAACCC[A/G]GGAGGCGGAGCTTGC | 55213 |
rs376186798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581830 | GTGGAGAAACTTCCA[C/T]TGGATTTAACAAGGA | 55213 |
rs376280880 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544497 | AAACAAACAAACAAA[A/C]AAACACAAAAAACCA | 55213 |
rs376337283 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544002 | TAGAACATTCTTCAA[C/T]TGGTAATTGCATGTC | 55213 |
rs376344517 | in-del | -/CTT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538823 | CTTTCTTTTTGTCTT[-/CTT]TCTATTCTCTAATTT | 55213 |
rs376473257 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558549 | ATACAAAAAAATTAG[C/G]CAGGCATGGTGGCAG | 55213 |
rs376578621 | in-del | -/TA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583385 | AAGTGTGCTTTTGTG[-/TA]TGTGTGTGTGTGTGT | 55213 |
rs376586330 | snp | C/T | 0.000197919 | 0.00994586 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566749 | AGACAGTTACTATAG[C/T]TCAGTCCAAATACAA | 55213 |
rs376618819 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566462 | CCAGAGTTAGCCCGA[A/C]GTGTTTAACTTTCAC | 55213 |
rs376684559 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568659 | AGGCCGGGGGAGGGG[C/G]GTGGCTCACACCTGT | 55213 |
rs376725258 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539109 | TCCTGATCTCAAGTG[A/G]CCCACCTTGGCCTCC | 55213 |
rs377026715 | snp | A/G | 1.68386e-05 | 0.00290155 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567131 | AAGTCCTAAAACGAA[A/G]CTAGGTTTCAAGAGA | 55213 |
rs377031516 | snp | G/T | 0.000134339 | 0.00819459 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555478 | CGTGTAATTGAAAAA[G/T]AAGGTAGAAAGGGAA | 55213 |
rs377062080 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565891 | AGAAAGAAGTAGACA[C/T]AGGAGACTCCATTTT | 55213 |
rs377081115 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547069 | AGTATATACAAATCT[A/G]AAGATGTGTACAGAA | 55213 |
rs377092157 | snp | A/C | 0.000384323 | 0.0138569 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540827 | AGCGGGGGAGACGAG[A/C]ACAAAGGGAGTTAAA | 55213 |
rs377096420 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539085 | ATGTTGGCCAGGCTG[G/T]TCTCAAACTCCTGAT | 55213 |
rs377136239 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535288 | CTGCCTATGCTAATC[A/C]ACCCTTTCATCCCCT | 55213 |
rs377330055 | snp | C/T | 3.30508e-05 | 0.00406501 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555510 | TGGGAGTGGAGACAC[C/T]TCACCTCGCCATTGT | 55213 |
rs377375340 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564965 | GCAGAACAAAGACCA[C/G]TGAGCTATTAAGGAA | 55213 |
rs377378257 | in-del | -/ATT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547953 | CCACCACTCCTGGTT[-/ATT]TTTTGTAGAGATGGG | 55213 |
rs377435647 | snp | C/T | 3.36055e-05 | 0.00409898 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566583 | AACCGGTCAATTTCT[C/T]ACAAACTGAAAAGTT | 55213 |
rs377438488 | snp | C/T | 0.000164823 | 0.00907659 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540909 | TGCAGCAGAGAATAG[C/T]GAAAAGGCATTCTCC | 55213 |
rs377448207 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547647 | GTACAGATTATGTAA[C/T]CAAATATCACCCCAA | 55213 |
rs377494249 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535581 | AGACAGAGTGGAAGG[C/G]GCCCACACAAACATG | 55213 |
rs377642222 | snp | C/T | 0.000150973 | 0.00868697 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560127 | AGCTCCAAAAAGAAA[C/T]AGTAACCCTGTACTT | 55213 |
rs377703528 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571759 | ATACCACCAAAACTT[A/T]CTAATTTACTCAAAA | 55213 |
rs377706589 | snp | C/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580738 | ATTTCATCTATTAGT[C/G]CCCAGTTGTATGAAA | 55213 |
rs377733039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574175 | CCAGTCTGGAGTACA[C/T]TGGCACCATCTTGGC | 55213 |
rs377736935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543059 | CCTGAGGTCAGGAGT[C/T]TGAGACCGGCCTGGC | 55213 |
rs386379141 | in-del | -/ACAT/AT/CA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538772 | TACACACACACACAC[-/ACAT/AT/CA]ATATATATATATGCC | 55213 |
rs386379142 | in-del | -/CT/T/TCT/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538888 | TAAGTTTTTTTTAAC[-/CT/T/TCT/TT]TTTTTTTTTTTTTTT | 55213 |
rs386379143 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547176 | ACAATACTCACTGCA[-/AA]AAAAAAAAAAAATAC | 55213 |
rs386379144 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547187 | TGCAAAAAAAAAAAA[-/AA]ATACTGTATTATACC | 55213 |
rs386379145 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559656 | CGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 55213 |
rs386379147 | in-del | -/AA | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586754 | TAAAAAAAAAAAAAA[-/AA]AGGTATTAAGAAACT | 55213 |
rs386770874 | multinucleotide-polymorphism | ACA/CCG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535149 | CACTAATATCTCAGA[ACA/CCG]TCACCCCCACAGAAG | 55213 |
rs386770875 | multinucleotide-polymorphism | AC/GT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539015 | GCTGGGATTACAGGT[AC/GT]GCACCACCACACCCA | 55213 |
rs386770876 | in-del | ACC/CT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552352 | GGAAGAGACAAAAAA[ACC/CT]AGCCCATCTAAACAA | 55213 |
rs386770877 | in-del | GAGAC/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563343 | GGTGACAGAGAGAGA[GAGAC/T]CCTGCCTCAAAAAAA | 55213 |
rs386770878 | in-del | AG/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563660 | CGAGACTGTCTCAAA[AG/T]AAAAAAAAGGAAAGA | 55213 |
rs386770879 | multinucleotide-polymorphism | CC/TG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567761 | CCACCAGCACCAACT[CC/TG]GATGACAAGGATCAG | 55213 |
rs386770880 | multinucleotide-polymorphism | GA/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585169 | GCACCTCAAAAAAGA[GA/TT]GGGAGGCAGGGAAAA | 55213 |
rs386770881 | multinucleotide-polymorphism | CA/TG | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586905 | ACAGCCTCCAAAGTA[CA/TG]CATCAGTTTCCTACT | 55213 |
rs397712424 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557766 | CTCTACAAAAAAAAA[-/A]TTTTTTTTTTAAAAG | 55213 |
rs397751915 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550000 | ATTTCTTTTTTTTTT[-/T]CTTTTTTGAGACAGG | 55213 |
rs397807681 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547188 | GCAAAAAAAAAAAAA[-/AA]TACTGTATTATACCT | 55213 |
rs397823323 | in-del | -/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584269 | ATCACTTGCAAAAAT[-/T]CTCTTTAAAGATGAA | 55213 |
rs397829400 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560627 | TTTTTTTTTTTTTTT[-/T]ACATAAAGCAACCAT | 55213 |
rs397840149 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552352 | GGAAGAGACAAAAAA[-/A]CCAGCCCATCTAAAC | 55213 |
rs397851340 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583390 | TGTGCTTTTGTGTAT[-/G]TGTGTGTGTGTGTGT | 55213 |
rs398022717 | in-del | -/A | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532416 | TAGTAAACATACTGA[-/A]GTTCACATTTTGCTC | 55213 |
rs398022719 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576206 | AAAAAAAAAAAAAAA[-/A]GTTGAGATGATTTTT | 55213 |
rs398022720 | in-del | -/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577535 | AGTTTAAATTGCTGT[-/T]ATGTACTGGCTTTTA | 55213 |
rs398022721 | in-del | -/C | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582828 | TCACCTATTTTTCCC[-/C]TATGAAGAAAGAGTT | 55213 |
rs398056378 | in-del | -/ACA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574935 | CTGATACATACAACA[-/ACA]GGGATGAACCCTGAA | 55213 |
rs527254040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573505 | CCAAGCTGGAGTGCT[A/G]TGGCACGATCTTGGC | 55213 |
rs527325142 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583657 | GGTCAGGTAATTCTC[A/G/T]TACCTCAGCCTCCTG | 55213 |
rs527347329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563593 | GAACCCAGGAGGCTG[A/T]TGTTACAGTGAGCTG | 55213 |
rs527437206 | in-del | -/A/AA | 0.0964426 | 0.197282 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559879 | TATTTACTATGATGA[-/A/AA]AAAAAAAAAAGAATA | 55213 |
rs527446413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576882 | AAAACAAGGGTGCAA[C/G]GAAAGAAAAGAGGAA | 55213 |
rs527449023 | in-del | -/CCGG | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539114 | TCTCAAGTGGCCCAC[-/CCGG]CTTGGCCTCCCAAAG | 55213 |
rs527501116 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548235 | CTCTACTAAAAATAT[-/A]AAAAAAATTAGCCAG | 55213 |
rs527546233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538775 | CACACACACACACAT[A/G]TATATATATGCCCTA | 55213 |
rs527570341 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583269 | CACTGAGCAGAGAAA[C/T]CTAGCAGGATGGTAA | 55213 |
rs527594005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539036 | CACCACACCCAGCTA[A/G]TTTTTGTATTTTTAG | 55213 |
rs527610033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576239 | TAAGTAGTCTAGAGA[C/T]TGATGGTGGTGATGA | 55213 |
rs527616231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583889 | AAACCAGAGAATATT[C/T]TGAAATGTGTCCGAA | 55213 |
rs527661360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565225 | TTTCGCTGTGTTGGC[C/T]GGGTTGGTCTCCAGC | 55213 |
rs527708485 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559566 | GAGGCTGAGGCAGGA[A/G]AATGGCGTAAACCCG | 55213 |
rs527825195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564945 | GGAACCCTGAAAGTT[A/G]CATTGCAGAACAAAG | 55213 |
rs527860400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584791 | TTGAAAGTGTCTTAC[A/T]TGCAAATAAATAAAA | 55213 |
rs527870235 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546748 | ATCTAATACCGCTGC[G/T]GATCTGATGGGAGGT | 55213 |
rs527914171 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539573 | GGAGCGTGGAGAGGC[C/T]CAGAGAGGATTCTAA | 55213 |
rs527934671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553145 | CAAGATCGTGCTACC[A/G]TACTCCAGCCTGGCA | 55213 |
rs528111919 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553676 | CACAGCAATGTAGGG[C/T]GGCAGACATAGACTG | 55213 |
rs528166905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535763 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 55213 |
rs528236920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573840 | CCAGTCTGGAGTACA[C/T]TGGCACCATCTTGGC | 55213 |
rs528259316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549804 | GCAACAAAAGCAACA[A/G]ATCAGGGCAAGAGCA | 55213 |
rs528297934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550351 | TTGGGCTGATAAGCA[C/T]TGGCTGGGGGTCACG | 55213 |
rs528587546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537366 | GAAAACATAATTTAT[C/T]CCATTACGCAAAAAA | 55213 |
rs528588857 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585635 | GCGCGCCCGGGACGC[-/T]ACCCAGCCGAGCATC | 55213 |
rs528612772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582025 | AGTAATCACAGAATG[C/T]GATAGAGTTGCAGGA | 55213 |
rs528781793 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532020 | TTACATACTAGAGTA[C/T]CAAACATTGTTCCAG | 55213 |
rs528797260 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569312 | GGCGCAGTAGCTCAC[G/T]CCTGTAATCCTAGCA | 55213 |
rs528957367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568556 | CACACACCCTTCCCA[C/T]ACAGCGTACTCTCAC | 55213 |
rs529046537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543512 | AGGAATGACATAGGG[C/T]TTTTCTGTTCCTTTC | 55213 |
rs529051009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582178 | AAGTAGCAGGGAATG[A/G]GATCTGAAGCAGAAG | 55213 |
rs529083995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544090 | AAGAGGGCATATACA[C/T]TTTTCAATAACAACC | 55213 |
rs529084271 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537432 | TTTGGCCCACCAAAA[A/G]AAGAAAAAAACGCTG | 55213 |
rs529095598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582666 | TTCTCTCTCCCCGCT[A/G]AGTCTCCATTTTACA | 55213 |
rs529096227 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559610 | GCAGTGAGCAGAGAT[C/T]GTGCCACTGTACTCC | 55213 |
rs529120426 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580005 | TTTCATCTCATTCAT[C/T]TCATCTCGTCTCACT | 55213 |
rs529161590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542756 | TCTTCCCAGGCCTGC[C/T]ACAAGCTTATTTATA | 55213 |
rs529237911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569355 | AAGCCGGAAGGACTG[C/T]TTGAGCCCAGCAGTT | 55213 |
rs529244301 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573702 | TGATCCACCTACCTC[A/G]GCCTCCCAAAGTGCT | 55213 |
rs529257007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576003 | CATCCTGGCTAACAC[A/G]GTGAAACCTCGTCTC | 55213 |
rs529273684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563259 | TTTAAAAATGAGGTG[A/G]GAAGATCGCTTGAGC | 55213 |
rs529273848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569711 | GGCAGAGTGAGAGAC[C/G]CTGTCTCAAAAAAAA | 55213 |
rs529305624 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557099 | TTGGTCTCCCTGAGC[C/T]TTTGGGTTTGTTCAC | 55213 |
rs529396862 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532061 | AAGAGTACATTTAGG[G/T]CTATCTTAAGAAATA | 55213 |
rs529496563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558207 | TCTAAGCTGTATACA[C/T]GTCTCAATGATTCTA | 55213 |
rs529505244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563928 | CTAGACAAAGAAAGG[A/C]CGGGATGCAAATCAT | 55213 |
rs529526053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551677 | AGGCCGAGGCAGGCA[A/G]ATCACAAGGTCAGGA | 55213 |
rs529627137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572182 | AAATACAGAAATTAT[A/C]CAGGAGTAGTGGCAT | 55213 |
rs529642625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572646 | TGTCTCCACTAAAAA[C/T]ACAAAAATTACCCCG | 55213 |
rs529642990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565997 | GAAACGTGCTGTGTC[C/T]ACTCAGGGTTAAATG | 55213 |
rs529658874 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563670 | TCAAAAGAAAAAAAA[C/G]GAAAGAAAGAACCAG | 55213 |
rs529721381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540468 | TGCAGAGCGTACACA[A/G]ATACAAATCATACAC | 55213 |
rs529799749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579214 | ACTCTATGGTATAAG[A/G]GCTGCAAATCACAGG | 55213 |
rs529824747 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532136 | TCAAATAAGAGTTGT[C/G]ATATCCTGCTATGAT | 55213 |
rs530051794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581161 | AACAGATGTAGGTCT[A/C]TGAAAGATTACTTTG | 55213 |
rs530140836 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545006 | TTGTTTGACAAATCA[A/G]TTCTACGGTATTAAA | 55213 |
rs530147283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542111 | CCCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA | 55213 |
rs530172326 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548538 | TACCCACGAGAGTCA[A/C]AGGTGGGAACAACCC | 55213 |
rs530277639 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539767 | TTTGATCATCATTCC[A/G]TCTGTTGTCGGGCTG | 55213 |
rs530302339 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574035 | GTGATCCACCCACCT[C/G]GGCCTCCCAAAGTGC | 55213 |
rs530316139 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567582 | TGCTTATCTGTTCCA[A/C]ATGTGCTTCCAACTC | 55213 |
rs530382798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542487 | AATGATGTACAGAAA[G/T]GCATTTTAAACAATA | 55213 |
rs530466751 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573464 | TTTTTTTTTTTTTTT[C/T]TGAGATGGAGTTTCG | 55213 |
rs530474059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581517 | GTGGACAAGTCCCAA[C/T]AGATGGATTTAGAAA | 55213 |
rs530548584 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567162 | CTCTTACCTCATCAT[C/T]GTCAGTAACGTACAG | 55213 |
rs530567477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572774 | ATGCAACTGTCCTGA[G/T]TGATAAGAGTGAGAC | 55213 |
rs530569357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559384 | GTTGTTGGCTGGGCA[C/T]GGTGGCTCACGCCTG | 55213 |
rs530667549 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573895 | TTCAAGCAATTCTTG[C/T]GCCTCAGCCTCCCGA | 55213 |
rs530768751 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582428 | GGAGACGGAGGTTGC[A/G]GTGAGCCAAGATCAC | 55213 |
rs530821153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581962 | AACCATGAGTATAAA[C/T]AACTTGTTCAAGAAA | 55213 |
rs530895025 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586574 | CAACATTACTGGAGG[C/G]TCTGGCTACAAATAA | 55213 |
rs531042079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542565 | TCAACATTAAAATGA[C/T]TCATTTGTTTTTTGT | 55213 |
rs531111630 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571085 | GGCGGGGTAGCTCAC[A/G]CCTGTAATCCCAGCA | 55213 |
rs531114641 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537955 | GCTATCTTGTCAAAA[C/G]GGGGCATGGAGGAAC | 55213 |
rs531148923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562164 | TCTCAAATAGAAGAC[A/G]CTGAATCCATGAAAC | 55213 |
rs531155128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568185 | TTTCCCTACTTAACA[A/G]TACATCGGGGAAATC | 55213 |
rs531214151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537265 | CAGTCTATAATTCAT[A/G]TTATAGCACATCAAG | 55213 |
rs531215700 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584561 | AATCATTTTTCCATT[C/G]CTTCCGGCATTATAT | 55213 |
rs531255677 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582489 | CAAAATTCTGTCTCT[A/G]AATAAATAAATAAAT | 55213 |
rs531345011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577123 | CATGAGGAAGAAAAG[G/T]TTATTTTACTTTATA | 55213 |
rs531378288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539075 | GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTCA | 55213 |
rs531514105 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534059 | ATCACCCGTAGAGCA[A/C]AAACTGGACACATCC | 55213 |
rs531514844 | snp | G/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545668 | GGCTAATGGGGAAAT[G/T]TTTTTAAATTCCAGA | 55213 |
rs531517796 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573450 | ACAATTCCTCATCTT[-/T]TTTTTTTTTTTTTTT | 55213 |
rs531549263 | in-del | -/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533191 | ACCACTTCTTCCAGT[-/C]ATATATAGTAGATAT | 55213 |
rs531560652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565260 | AACCGCGAGTGATCT[C/G]CCAGCCTCGGCCTCC | 55213 |
rs531640221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553656 | TTTGTGGTGGCATCG[A/C]GCCCCACAGCAATGT | 55213 |
rs531726966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553222 | AAAGTGACAAAAAAC[A/C]TACCAGGGAAAGTGC | 55213 |
rs531728805 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539890 | TCAACTTTGATCCCT[A/G]TGTGTGATGAAGTGT | 55213 |
rs531731889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559463 | AGATCGAGACCATCC[C/T]GGCTAACACGGTGAA | 55213 |
rs531790415 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542163 | AGGTTGTGGCGAGCC[A/G]AGATTGCGCTTCTGC | 55213 |
rs531802341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565787 | AGCTCATTGAGAACA[A/G]GCCATGATGACGATG | 55213 |
rs531827529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534790 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 55213 |
rs531830199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541314 | TACTAGAAAATTAAA[A/G]TAAGCCCATAGCTTA | 55213 |
rs531903711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579280 | TATTGCCCCAGCTGC[C/T]AGAACAGCTGTCATC | 55213 |
rs531950460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579820 | AATTCTCTGATTGTG[C/G]CTACCCTTTGTTTCA | 55213 |
rs531987529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579138 | CCCAGGTCCAGATAA[A/G]CCTCTAAGAATCAGC | 55213 |
rs532026029 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567569 | ACTTCCTAGTCAGTG[C/T]TTATCTGTTCCACAT | 55213 |
rs532041347 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548321 | TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAGC | 55213 |
rs532076176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585194 | GGGAAAACTTTCCCT[A/C]GCCTCTCCCCATCCT | 55213 |
rs532105648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584736 | TTACAAGACTGCTTT[A/G]TAAAATTGTAATCCC | 55213 |
rs532119074 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539341 | CATGTTTATACTTAA[C/T]ATGAGAAAAATGAAA | 55213 |
rs532140345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571583 | CATTAGACCATGCAT[A/G]CTCAACCTGGGCAGC | 55213 |
rs532186727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565890 | TAGAAAGAAGTAGAC[A/G]TAGGAGACTCCATTT | 55213 |
rs532424350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534562 | AAGAATTTCCTGCAC[A/G]ATTATCACATAATCT | 55213 |
rs532497288 | in-del | -/TAAA | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567353 | ATTCCAGAAAAAAAT[-/TAAA]TAGTCACTGAGCTAA | 55213 |
rs532501067 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570729 | CAGGAAAGAAGAAAC[A/G]AATAACTATCCTGAA | 55213 |
rs532539846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554299 | TATCTGTTTCACTTG[C/T]CTTCCTTTACTTTGT | 55213 |
rs532590438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559695 | GTTGTCAGGGGCTGG[A/G]GGAGGACAGAATGGG | 55213 |
rs532659052 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541403 | TAACAAGCCTACACA[A/T]CCTGCACGTGTACCC | 55213 |
rs532679250 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585870 | TGCTCCCCGAGATGG[C/T]TTGGCTGTGGGGAGG | 55213 |
rs532717034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572922 | AGGCACTGCTAATGG[A/G]AAGAACCTTCAACTG | 55213 |
rs532719001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580950 | GCTGGTCAGATGCTG[C/T]GGAGGCAACAGAATT | 55213 |
rs532787902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550567 | TTTAAACAGATAATG[G/T]CCTTTCAAGAGCAGA | 55213 |
rs532790877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535871 | CTACTAAAAATACAA[A/T]AATTAGCCAGGTGTG | 55213 |
rs532886620 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586364 | GCTCTCGGAGAACTC[C/G]CAGTTGGCGCTGCAG | 55213 |
rs532981910 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551121 | GGAAGGGAAGGGAAG[C/G]GAAGGGGGGAGGGAG | 55213 |
rs532999877 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532142 | AAGAGTTGTCATATC[A/C]TGCTATGATTAACAA | 55213 |
rs533019607 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556488 | AGCCACCATGCCCAG[C/G]CTCATGGAAACCATT | 55213 |
rs533067587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537984 | ACCTCAGGTACTTTC[A/G]TAGAAAGACAAGAAA | 55213 |
rs533128752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583154 | TACTCCAGACTGGGC[A/G]ACATAGTGAGACCCT | 55213 |
rs533128884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575674 | GTTGTCACTTAGAAA[C/T]GGGAACTAAATATAG | 55213 |
rs533166534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576124 | CCTGGGAGGCGGAGC[C/T]TGCAGTGAGCCAAGA | 55213 |
rs533171502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557766 | TCTCTACAAAAAAAA[A/T]TTTTTTTTTTAAAAG | 55213 |
rs533230938 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532890 | TAAAAGCAAGCTCAA[C/T]GGACACACATGATGA | 55213 |
rs533295550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582799 | TGGCATTTGGAGACC[A/G]TTCTCTTCTGAGGTC | 55213 |
rs533346615 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536770 | AACTCTGTTTATGAC[A/G]TTATGTGGCAGAACA | 55213 |
rs533576182 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531666 | TTGGGGACCCCTGAC[C/T]TAAAGGACTCTTCAT | 55213 |
rs533750469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564213 | GCAACTACATGAATG[A/C]CAGAGAACAGATGAA | 55213 |
rs533818599 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532420 | AAACATACTGAAGTT[C/T]ACATTTTGCTCAGAT | 55213 |
rs533838219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543699 | GGAACTATATCTTAA[A/T]AACTTTTTTTTTCAT | 55213 |
rs533925394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582295 | AGTTCGAGACCGGCC[C/T]GGCCAACATGGTGAA | 55213 |
rs533950044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545531 | TGATAAGAAGAATTG[A/C]TGTTGTGGTTATATG | 55213 |
rs533950104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552665 | TGATGGGTAGCAAGT[A/G]CTACAATAGGTATAA | 55213 |
rs534106510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577544 | TGCTGTTATGTACTG[A/G]CTTTTAAATGCCACC | 55213 |
rs534138775 | in-del | -/CG | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534506 | TCTTCAAAACACACA[-/CG]CGCGCGCGCACACAC | 55213 |
rs534246841 | in-del | -/CAATTCCCGGCCAGGGC | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558078 | AATGAGAAAAAATGT[-/CAATTCCCGGCCAGGGC]CACTGTCTGTGGAGT | 55213 |
rs534260267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584186 | CAAGCTTGACAGCTT[C/T]GGGTTTTTATGGCTA | 55213 |
rs534329356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554875 | ACCAATGCATGATGC[C/T]AAAACATCTGTGTCC | 55213 |
rs534415611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578424 | GACTTTAATAGCATA[C/T]ATTAATTCTTCTTCT | 55213 |
rs534556651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549405 | GACACAGGAAAACTG[C/G]TCAGTTGGTAGTACC | 55213 |
rs534613566 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586118 | ACTAGGGAAGGTGGC[A/C]GCTGGACAAAGGTAT | 55213 |
rs534617235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580457 | GTCATAATGGTGTGC[A/G]CCTGTAGTTAGTCCC | 55213 |
rs534636863 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532570 | ATTCACTGGGCTTCA[A/G]TCACTTGTGATATGG | 55213 |
rs534674934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560906 | TATGCGGGGATGAGG[A/G]GTGCACGGAGCTCCC | 55213 |
rs534782283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573618 | CACGCCCGGCTAATT[C/T]TGCATTTTTTTAGTA | 55213 |
rs534806865 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542209 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 55213 |
rs534886750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556583 | TTCCTCCAACATTAG[C/G]AAATGTCTAAGCCCC | 55213 |
rs534905151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551093 | GGGTGACAGAGACTC[C/T]GTCTCAAAAAAGGGA | 55213 |
rs534922821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543004 | GCTCAAGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 55213 |
rs534928710 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586801 | TGAGCTTAGTTCTGT[A/G]TCTATTCTGAGGTCT | 55213 |
rs535045246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562271 | AAATTTGACATAAGC[A/G]TTGTAAGATAAAGTT | 55213 |
rs535111926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542304 | ACCCAAAAAACATTC[C/T]ACATGCAAGTGGTTT | 55213 |
rs535157630 | in-del | -/T | 0.43555 | 0.167544 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576842 | AGGTGAATCAATGAC[-/T]TTTTTTTTTTAACTG | 55213 |
rs535211275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550109 | ATCCTTCCACCTCAG[A/C]TTCCCAGACCACAGC | 55213 |
rs535220990 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575702 | TAGGGTACACGTGGA[C/T]ATAAAGACAGGAACA | 55213 |
rs535249582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550709 | ACTGCAGTAATTATA[C/G]CAAGATGCATTCACA | 55213 |
rs535257207 | snp | C/T | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549110 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGATTC | 55213 |
rs535264795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566227 | ACCCTGCCAAATCCC[C/T]CTATGCGAGAAACAC | 55213 |
rs535275247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568328 | ATTCCAGTCTTTTGC[C/T]AGAACAATAGTGCAA | 55213 |
rs535357605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536306 | AAGGAAGCCCTGAAC[A/G]CATGTGGTGAGGGAC | 55213 |
rs535383241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556106 | GCGGTATATGCCACA[C/T]AAGTATTAGTGATGT | 55213 |
rs535407058 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586887 | TGGCTCTGGTTTTCT[G/T]CAACAGCCTCCAAAG | 55213 |
rs535445464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562428 | GCCCAGGAGGTTACA[A/G]GTGTGAACCACCTGC | 55213 |
rs535492499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554983 | TCCAGAGACTAATTT[C/T]ACAGAAATAACCATC | 55213 |
rs535602260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568669 | AGGGGGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55213 |
rs535623317 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541274 | GTTTCTAAAACGCTA[A/G]ATGCATTAGCAACTT | 55213 |
rs535725373 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587221 | TAATACTCACTGAAT[A/G]AAGTGGCTTGCCCAA | 55213 |
rs535748021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536901 | TCATTCCAAATCTTT[C/G]AACATTGAAACTATT | 55213 |
rs535755487 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581629 | AGAGCAGAGTACCTT[-/AAG]AAGAACTCTAAGAAA | 55213 |
rs535775332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581728 | GAAAACCAGGAGACA[C/G]AGTGTCACAGAGATC | 55213 |
rs535823131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548413 | AAAAAAAAGAAAAGA[A/G]AGTTCATCTTTGATT | 55213 |
rs535859397 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546498 | AGCACATTATGTTTA[C/T]TGTGCACTTAATTTT | 55213 |
rs535860793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556641 | CAGGAGGTGGTCCAC[A/G]TATATACTGAGTGTG | 55213 |
rs535991222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565005 | AGCTGTCCCGCTCCC[A/G]CTCCCATTCCCACTC | 55213 |
rs536051673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543796 | GCTCAAGCAATCCTT[C/T]CACCTCAGCCTCCAG | 55213 |
rs536090366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544423 | GCGGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 55213 |
rs536103351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550793 | TCATGTTCATTCTGG[A/C]TACTACTCAAAACAC | 55213 |
rs536245903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534895 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGATGCCT | 55213 |
rs536381499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579443 | CCTGGCTAACACAGC[A/G]AAACCCCGTCTCTAC | 55213 |
rs536425452 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553929 | GATACACATACACAG[A/T]GTAACATAGAAAATC | 55213 |
rs536432176 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559972 | ACAAGCTACTTCCAC[C/T]ACTTGCTTGATCAAG | 55213 |
rs536440612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583794 | CTCGTGTAATCTGTC[A/G]CCTCAATCTCCCAAA | 55213 |
rs536468216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548020 | CTGAGCTCAAGCAAT[C/T]CACCCACCTTGGCCT | 55213 |
rs536489181 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533890 | TCCAGCCCAAATTTA[A/C]GAAAGGTCACATTTA | 55213 |
rs536517049 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581350 | AAGGAGCACTGGATA[A/T]GCAGAAAGGCAGAGC | 55213 |
rs536590161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559513 | TACAAAAAATTAGGC[A/G]GGTGTGGTGGTGGGT | 55213 |
rs536622901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580188 | AAAAGAAATATCGAT[G/T]ATTAGAAATAATGTT | 55213 |
rs536683074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535510 | GAACCAGAAGCTCAA[A/C]ATTTCAACTGCAGGT | 55213 |
rs536700657 | snp | A/G | 3.33606e-05 | 0.00408401 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540831 | GGGGAGACGAGCACA[A/G]AGGGAGTTAAAGGTG | 55213 |
rs536793473 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585908 | TACCACCCCAGAGAC[C/T]TAGGACGGAAAAGCG | 55213 |
rs536819898 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585958 | TGCCCACTCTAGAGC[A/G]CGTCTGGCCCCGGGG | 55213 |
rs536826844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567357 | CAGAAAAAAATTAAA[C/T]AGTCACTGAGCTAAC | 55213 |
rs536955344 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585475 | TGCCGCGCCGTCCCG[C/T]GGGACCGCAGGGATC | 55213 |
rs537015732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566948 | TTTCAGAATGTTTGT[C/T]TATATTATGAAACTC | 55213 |
rs537141007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580309 | TGGATAGATGGCTGG[A/G]TGAAGTGGCTCACAC | 55213 |
rs537239042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571727 | TTCCCTCCTAAGGCA[A/G]CAGAGCGTAACTGTA | 55213 |
rs537247683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548656 | ACAGAGACATATTAC[A/G]TCAATGGGCCTCAAA | 55213 |
rs537279024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541553 | AAAGATACTTACTTC[A/C]AATCTTTTTTAAGCA | 55213 |
rs537350698 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549350 | ACGTATGAAAGCTAA[C/T]AGAGAATAAAACATT | 55213 |
rs537408368 | in-del | -/TAAATAAA | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582488 | GCAAAATTCTGTCTC[-/TAAATAAA]TAAATAAATAAATAA | 55213 |
rs537414585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576391 | GGGCTTTTATCAAGA[C/G]TGCATTAATAAACTC | 55213 |
rs537419812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573593 | AGCTGGGATTACAGG[C/T]GCCCACCATCACGCC | 55213 |
rs537450701 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569907 | AGGGAGACCCTGTCT[C/G]AAAAAGATTAATAAA | 55213 |
rs537493249 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551250 | GAATCACAAAGCCAA[A/C]CACCACAGCTCTGCC | 55213 |
rs537508614 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568034 | TCCTTATCATCCCTC[C/G]CTGACCCTCTCCTCA | 55213 |
rs537552055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536007 | CAGCCTGGGAGACAG[A/G]AGTGAAACTCCATCT | 55213 |
rs537582261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583333 | CTTTAGAGGTACCCA[C/T]CTGGTCTCCTCTGTG | 55213 |
rs537663974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556010 | TTGACCACCATGCTA[C/T]ATTCCCTCTATAATT | 55213 |
rs537782784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560691 | TGGACAGGGGACAAT[A/G]AAGATGGCTTGTCTT | 55213 |
rs537850736 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546301 | CATGTGACTTTCCGT[C/T]TAACACTCAGATGAG | 55213 |
rs537910771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538235 | CTAGCCTCAAGCAAT[C/T]CTCCCACTTCAGCAT | 55213 |
rs537914369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552698 | AAGGCGCTGCAGAAC[A/G]GCAAGGAGGAAGGCT | 55213 |
rs537950147 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532446 | CAGATCATAAGCCTA[C/T]AGAACAGTGATTGTT | 55213 |
rs538024848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557839 | ATACACGTTATGCTA[A/G]AGAGAGAGTGCACTC | 55213 |
rs538058159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565495 | TCTGGGATGTGAGGA[A/G]CCCCTCTGCCCGGCT | 55213 |
rs538152636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534454 | ATACTATTTATTCAA[C/T]GCAGTAAAAGCAATG | 55213 |
rs538199296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584330 | CGGGTAGAAGAAAAA[G/T]GACCCGTCTAGAGTA | 55213 |
rs538213486 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561103 | TTCCACAGCACCCCC[A/G]AGTGCCAAGGGCAGG | 55213 |
rs538223664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570865 | TGAGGACTGAGGCTC[A/G]AAGGTGAAATGACGC | 55213 |
rs538270618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546845 | CACTCACCTCCTGCC[A/G]TGCAACCCAGTTAAT | 55213 |
rs538287342 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574890 | GGTCTACACATACGA[C/T]AGAATATTATTCACC | 55213 |
rs538302561 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536240 | GAAAACAATCTAAAT[C/T]TGGGTTGTGTAAGTA | 55213 |
rs538386160 | in-del | -/CAGA | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539783 | TCTGTTGTCGGGCTG[-/CAGA]CAAAGTCAGCTACAT | 55213 |
rs538644681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539789 | GTCGGGCTGCAGACA[A/G]AGTCAGCTACATTTG | 55213 |
rs538645333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550969 | TTAGCTGGGCATGGT[A/G]GTACACACCTGTAAT | 55213 |
rs538682602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534507 | TCTTCAAAACACACA[C/T]GCGCGCGCACACACA | 55213 |
rs538701538 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533258 | ATACTATACATGTCA[G/T]TATTTTCCTCTTAAG | 55213 |
rs538812924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552883 | AACTGCGGTAGTGGT[A/G]GTAGAAAGACTAGAA | 55213 |
rs538813218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559372 | ACAGAGTAGAAAGTT[A/G]TTGGCTGGGCACGGT | 55213 |
rs538899810 | snp | G/T | 1.66635e-05 | 0.00288643 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566606 | GAAAAGTTAGATGGG[G/T]TCCCTCCTTACCTTC | 55213 |
rs538920869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534863 | ACATAGGGAAACCCC[A/G]TCTCTAGTAAAACTA | 55213 |
rs538975339 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585330 | CCCGAGCGAGGGAGG[C/T]GGGAGGTACAGGAGT | 55213 |
rs538986575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578790 | GATCATCCAGTTTCC[C/T]AGAAGAACAAAGTGT | 55213 |
rs539082655 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537007 | CAGAGCATTGATGGT[A/C]TTAATATCCTCATTT | 55213 |
rs539091671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547721 | AAATAAAAGAATTTG[A/G]AATCAGTTGAAAGAC | 55213 |
rs539218943 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546811 | CAGCTGTAAATACAG[A/C]TGAAGCTTCGCTCAC | 55213 |
rs539259923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569407 | GGCGAAACCCCATTT[C/T]TACAAAAAATACAAA | 55213 |
rs539291650 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556411 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCACG | 55213 |
rs539327275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571745 | GAGCGTAACTGTAAA[C/T]ACCACCAAAACTTTC | 55213 |
rs539329504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579346 | AATGAAAGGGAGGCC[A/G]GGCGTGGTGGCTCAC | 55213 |
rs539343612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574307 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 55213 |
rs539350041 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531645 | TATGGGTCTGTGGCC[C/T]GAGGGTTGGGGACCC | 55213 |
rs539366991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572314 | CCTAGGCGACAGAGC[A/G]AGACTCTGTCTCAGA | 55213 |
rs539425681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557393 | ATGGTACAAAAGATT[A/G]GAAGACAGAATCAAT | 55213 |
rs539480022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550043 | CACCCAGGCTAGAGC[A/G]CAGTGGCATGACCAT | 55213 |
rs539483219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568294 | TTACCTTATTTTCTA[C/T]TGAGAGACATTTAAG | 55213 |
rs539585076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556876 | AATCAGGAACCCAGC[C/T]GGCATAAATTAGCAA | 55213 |
rs539633822 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545247 | ACTAAGAATATCTTT[G/T]TTCTGCTTTGGGGTA | 55213 |
rs539759161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582998 | CCTGGGCAACATAGG[C/G]AGACCCTGTCTCTAC | 55213 |
rs539802390 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547825 | ACAGGGTCTCGCTGT[C/G]TCACCCAGGCTGGAG | 55213 |
rs539883749 | in-del | -/A | 0.00178096 | 0.0297877 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541880 | CAATTTTTAAAAAAG[-/A]AAAAAAAATTACCTA | 55213 |
rs540043865 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535056 | CCAAAAAATTCACCT[G/T]AAATTCACTTTTATG | 55213 |
rs540195836 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575413 | CTGGGTATACATCCA[A/G]AGGAAAATAAATTGT | 55213 |
rs540287761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544037 | AGAAACAGAAGCACA[A/G]CATTCCTATGAGAGT | 55213 |
rs540314326 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573674 | AGGCTGGTCTCAAAC[C/T]CCCGACCTCAAGTGA | 55213 |
rs540367389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568026 | AGAAAGTCTCCTTAT[C/T]ATCCCTCCCTGACCC | 55213 |
rs540367390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574394 | AAAGTGCTGGGATTA[C/G]AGGCGTGAGCCACCA | 55213 |
rs540482135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564571 | GCCTGGAGACAGAGC[A/G]AGACTCCTTCTCAAA | 55213 |
rs540523804 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575868 | ATGTAACAAACCTGC[A/C]TATGTACTCCCTGAA | 55213 |
rs540560901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569643 | ATCACTTGAGCCCGG[A/G]AGGCAGAGGTGGCTG | 55213 |
rs540587185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579140 | CAGGTCCAGATAAGC[C/T]TCTAAGAATCAGCCT | 55213 |
rs540648811 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540460 | AATAGAATTGCAGAG[C/T]GTACACAGATACAAA | 55213 |
rs540742827 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556198 | TGTTTTGCTTTGGTT[-/T]TTTTTTTTTTTTTTT | 55213 |
rs540743069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582576 | AAGAGGAGGAGGAAA[A/G]GGTGAATGTGAATGA | 55213 |
rs540792820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585127 | CCACAGCAGTCAGAC[C/T]TCAGCTACGAGCAAA | 55213 |
rs540809262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547299 | CTTGCCTCCATGCCC[A/G]TGACTGGTCACCTAA | 55213 |
rs540816759 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533322 | TTTAAACTTGAGTTC[A/T]CAAGTTCTACCTTAA | 55213 |
rs540856420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566932 | GTGGACATTGCTTAC[A/G]TTTCAGAATGTTTGT | 55213 |
rs540878430 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559718 | AGAATGGGAGTGAAT[G/T]TTTACCAGGGACAGC | 55213 |
rs540955981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576531 | TAGGGAAATTCTCAA[C/T]GGAGCATTTATAAAA | 55213 |
rs540963030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572589 | AGGCAGATCAGTTGA[A/G]GTCAGGAGTTTGAGA | 55213 |
rs540984471 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585503 | ATCTCCGAAGCTCCA[A/G]TGGGCGCAGAAGTGC | 55213 |
rs541037555 | snp | C/T | 0.000198268 | 0.00995464 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540963 | GTGCTGACAAAGTTT[C/T]TTCAGTCTGTTTTCA | 55213 |
rs541049149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534592 | TAGTTATGCTCAAAG[A/G]CATTGTTGTAAAAGG | 55213 |
rs541279300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535015 | CTCTAGCCTGGGTGA[C/T]AGAGCAGAGGCTCTG | 55213 |
rs541403351 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542052 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAATTA | 55213 |
rs541480336 | snp | A/G | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548931 | TGAGGTCAGGAGTTC[A/G]AGAACAGCCTGGCCA | 55213 |
rs541483621 | snp | C/G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584814 | AAATAAAAACAAAAG[C/G/T]CCACTTATGCGAGCA | 55213 |
rs541504977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567035 | CAAAGCCATAGTCTT[C/G]CTGAACTTCAGGATC | 55213 |
rs541525332 | snp | C/T | | | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544860 | GTTAAAAAGTCTTCA[C/T]GCTCTGAAGGCAACA | 55213 |
rs541574637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581471 | GAGTCCTACTATGGA[A/C]ATTTGTGCCAGGTAC | 55213 |
rs541581073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579764 | TGAGTGAAGATAATA[C/T]CCCCACCTTCATTTA | 55213 |
rs541594593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560258 | AGATGGGTGACAGAA[C/T]GGGATAGACAGATGC | 55213 |
rs541594814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542438 | TTTCCATTTGATGGT[A/C]CCCAAGATTTTTTTG | 55213 |
rs541629470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536432 | GACAAACGCCCTTCC[A/G]ACTTGACCTCTCTTT | 55213 |
rs541767528 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49580561 | CCACTGTATTCCAGT[C/T]TGGGCAAGAGAGCAA | 55213 |
rs541791491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573678 | TGGTCTCAAACTCCC[A/G]ACCTCAAGTGATCCA | 55213 |
rs541861757 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537956 | CTATCTTGTCAAAAC[A/G]GGGCATGGAGGAACC | 55213 |
rs541939763 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585615 | CTCACGTGACCCGGT[A/G]CAGCGCGCGCCCGGG | 55213 |
rs542101033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573198 | TTATAAAACAATATG[C/T]CCTGTATGATTACAA | 55213 |
rs542193072 | snp | A/G | 0.000165796 | 0.00910333 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549613 | GTCTTGGCTGCAGAC[A/G]TGTGGGCAGAGTGAC | 55213 |
rs542243199 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533618 | CTGAAACAATCTTAA[C/T]TATTCCTTCACAGTA | 55213 |
rs542367503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574540 | TAGAAGTTTTAAGAT[G/T]TATTCTTGCTTTAGA | 55213 |
rs542417249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577905 | GCATTTACACATACA[C/T]TGAAAATTCCTAATA | 55213 |
rs542476835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537594 | GATTTCTGGAAAGTT[A/C]TCTACTCTGGTTAAA | 55213 |
rs542509763 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571005 | TTTCTGACTTTATCT[C/T]GCCTTGTAAATGTAC | 55213 |
rs542511178 | in-del | -/AAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551915 | AAAAAAAAAAAAAAA[-/AAA]GCATTAGAAAAGCCT | 55213 |
rs542529190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581908 | GGAAGAGGCCAGGTT[A/G]CAGCAGGTTGAGGCG | 55213 |
rs542578586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584480 | TAAACGGGTGAAATT[C/T]ACCCAGTGCTCACTT | 55213 |
rs542626763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552343 | TGGTAAGAAGGAAGA[A/G]ACAAAAAAACCAGCC | 55213 |
rs542722427 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578512 | TCTGCCTCTGAGGAA[C/G]TGAAGGTCTAATGGA | 55213 |
rs542766693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585004 | ACGATAAAGAATACG[A/G]TTTGTGACAGCACTA | 55213 |
rs542846741 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582445 | TGAGCCAAGATCACA[C/T]CACTGCACTCCAGCC | 55213 |
rs542870012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554094 | AGACACAGATAAACA[C/T]AGGATGCTATACAGG | 55213 |
rs542891331 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583912 | TGTCCGAATGCCCTG[A/C]CTAGATTCTAGACTC | 55213 |
rs542900520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546549 | ATGTAATGAAATAAT[A/T]ACACAACTCACCATA | 55213 |
rs542996147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553627 | AAGGCCTTGCTCAAA[C/T]TACAAACCCAAGATT | 55213 |
rs543012978 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565756 | GCCGCCACCCCGTCT[C/G]GGAGGTGTACCCAAC | 55213 |
rs543037117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546656 | ACAGATCATCTAGGC[A/G]TTAGATTCTCATAAG | 55213 |
rs543077281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534513 | AAACACACACGCGCG[C/T]GCACACACACACACA | 55213 |
rs543103942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578900 | TCTGAATCCATTTAA[C/T]TCCAGAAAAACATTC | 55213 |
rs543108343 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575287 | TACAGCAGAGGCAAC[A/T]CTATACACTGTTAGT | 55213 |
rs543175786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571774 | TCTAATTTACTCAAA[A/T]TTACCACCATCCTCA | 55213 |
rs543188938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554175 | ATCATCCCATTTTTT[A/T]AAAAAAAGATAATTA | 55213 |
rs543200725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553051 | GCTGGGCGTGGTGGC[A/G]CGTGCCTGTAACCCC | 55213 |
rs543291274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585051 | GAGAGATGCTAAGAT[C/G]TTGGAAAGGAGAGAG | 55213 |
rs543343068 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542586 | TGTTTTTTGTTTTAC[-/ATA]ATAAGCATATTCTTA | 55213 |
rs543469844 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568715 | GTGGGCAGATCAGGA[A/G]GTCAAGAGATCGAGA | 55213 |
rs543701909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540228 | ACTATAGGGTATACA[A/G]ACGAATGAGACAGTT | 55213 |
rs543704079 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577211 | TTTAGAACTGGAAGG[C/G]TGAAGGAGTAATGTA | 55213 |
rs543803226 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559644 | CTGGGCGACAGAGCG[A/G]GACTCCATCTCAAAA | 55213 |
rs543803408 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559642 | GCCTGGGCGACAGAG[A/C]GAGACTCCATCTCAA | 55213 |
rs543824525 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564766 | CATGGTGGCGGGCGC[C/G]AGTAGTCCCAGCTAC | 55213 |
rs543831299 | snp | C/G | 1.7486e-05 | 0.00295681 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549447 | GTGGAGGTGGCCCTG[C/G]ACTTTCTTACCCACA | 55213 |
rs543842237 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586202 | CCTCGGAAGCATGCC[A/G]TAGAGGTTAGACGGG | 55213 |
rs543867640 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547080 | ATCTGAAGATGTGTA[C/G]AGAAGTGCTTCAGCT | 55213 |
rs543967900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575164 | AAAAATATTCAACAT[C/T]ACTAATCATCAGAGA | 55213 |
rs543973611 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549057 | AAATCTCTTGAACTC[A/G]GGAGGTGGAGGTTGC | 55213 |
rs544009323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541985 | CTTTGGGAGGCCAAG[C/G]GGGTAGATCACCTGA | 55213 |
rs544063377 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551529 | GGCAGGGAGAACATC[G/T]ACTTAAAGGCTATAG | 55213 |
rs544205848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557036 | GTGGATCTGGGGCAT[G/T]AGGCCTGTGTGCTAT | 55213 |
rs544227829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557581 | ACACTGTCACACATC[C/T]GAGCTATAGTCTTAG | 55213 |
rs544235658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576621 | ATTGCTAAGATGACA[A/G]GTCCTTCCAGGGCTT | 55213 |
rs544307831 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533491 | CTTGACTAACCTAGA[A/G]TATTTATCTTTACAT | 55213 |
rs544321048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568562 | CCCTTCCCACACAGC[A/G]TACTCTCACGGCATT | 55213 |
rs544370892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565092 | CTGTACTGCTGCCAT[C/G]TCGGCTCACTGCAAC | 55213 |
rs544532717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564764 | GGCATGGTGGCGGGC[A/G]CCAGTAGTCCCAGCT | 55213 |
rs544570132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570298 | CAAGCTAACCTTCAT[A/G]ATGATGGGGCATTAT | 55213 |
rs544584726 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532830 | GGGAACTCACTCAAA[C/T]GGAAATGAGTTCATG | 55213 |
rs544697868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583106 | AGCCTGGGAGTTTGA[A/G]GCTGCAGTGAGCTAT | 55213 |
rs544711466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576038 | AAAAATACGAAAAAA[G/T]TAGCCGGGTGTGGTG | 55213 |
rs544765805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569585 | CCTGGCGGTAGTGGC[A/G]CATGCCTGTAATCCC | 55213 |
rs544867390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582252 | AGCACTTTGGGAGGC[C/G]GAGGCAGGTGGATCA | 55213 |
rs544891372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539027 | GGTACGCACCACCAC[A/G]CCCAGCTAATTTTTG | 55213 |
rs544893258 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560482 | CAAGTCACGGGGAAC[C/G]CACAGGGGGCGTGTG | 55213 |
rs544899834 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573594 | GCTGGGATTACAGGC[A/G]CCCACCATCACGCCC | 55213 |
rs544990405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557644 | TGAACTCTAGGTTGG[A/G]TGCGGTAGCTCACAC | 55213 |
rs545000198 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533892 | CAGCCCAAATTTACG[A/G]AAGGTCACATTTAAA | 55213 |
rs545022219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558029 | AGGTCCTTGAAAAAC[A/G]TCATTTCATTCAACA | 55213 |
rs545026943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551619 | AAAAAAGCATTAGAA[G/T]GCCGGGCGTGGTGGC | 55213 |
rs545042240 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557767 | CTCTACAAAAAAAAA[A/T]TTTTTTTTTAAAAGA | 55213 |
rs545068905 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542259 | ACTATCTGGGCCTGA[A/T]CACACCAGGATCACA | 55213 |
rs545203544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553561 | TAGGTTTGACAGGAG[G/T]GTTAAAGGTTCCAAA | 55213 |
rs545323043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558926 | GATTCACCATAAATT[A/G]GGTAAATAATTCTCT | 55213 |
rs545360085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552120 | CCTCCAATATTTCTC[C/G]AAGTTAGAGCAAGGA | 55213 |
rs545366755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565163 | GCGATTGCAGGGGCG[C/T]GCCGCCACACCTGAC | 55213 |
rs545395280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536348 | CAAGTTCACCAGAGA[A/G]TCGCACAGTCAAGCT | 55213 |
rs545454699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535852 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55213 |
rs545461089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584417 | AGATGAACTGTTATA[G/T]TAATAGAATCCAAAT | 55213 |
rs545523866 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545078 | AAAGATGGTATTTAG[-/A]AAGGCTAAATACCAT | 55213 |
rs545531697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577840 | CTACTCAAAACAGCA[A/G]CTTCTAATATGCAAA | 55213 |
rs545542852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542421 | TAGCACTTCCACTAC[C/T]GTTTCCATTTGATGG | 55213 |
rs545550799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559438 | AAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG | 55213 |
rs545561895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561846 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 55213 |
rs545594762 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556329 | CCAAGTAGCTGGGAC[A/G]ACAGGCGCCCGCCAC | 55213 |
rs545673863 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537641 | GCTGTTTCTCTTAAC[A/G]TTCAAATACACATAA | 55213 |
rs545832056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581972 | ATAAACAACTTGTTC[A/G]AGAAATTTCACTCTG | 55213 |
rs545855785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550867 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTAGATCA | 55213 |
rs545892969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580908 | TTGGGGGATCTAGAC[A/C]CATAAACAGATGCTC | 55213 |
rs546007878 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567460 | TGGATCACTCACTTT[-/C]CCCCCAGCCATGTGT | 55213 |
rs546065739 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582519 | TAAATAAATGCAAGA[G/T]AAACTGTAGAAAGGA | 55213 |
rs546233521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537269 | CTATAATTCATGTTA[C/T]AGCACATCAAGTACA | 55213 |
rs546456410 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532595 | ATATGGTCAAGAAAA[A/G]GGGGCTGGGGCTCCT | 55213 |
rs546537281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549892 | GATCACACAGACCGC[C/T]GAGGAAAACTTGGAA | 55213 |
rs546541874 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545036 | AGTAAGTATCCTGCA[C/T]CTATAAACTACCAAA | 55213 |
rs546710881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560474 | CCAAATACCAAGTCA[C/G]GGGGAACCCACAGGG | 55213 |
rs546711002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574715 | CATTAGAATTATATT[A/G]TCTAGATAAACTCCA | 55213 |
rs546771798 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542127 | GCTGAGGCAGGAGAA[G/T]CGCTTGAACCCGGGA | 55213 |
rs546781687 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554301 | TCTGTTTCACTTGTC[C/T]TCCTTTACTTTGTTA | 55213 |
rs546808805 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569122 | GGCAACCTGAAGCCT[G/T]AGTCTGAACTCTTCA | 55213 |
rs546882890 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559573 | AGGCAGGAAAATGGC[A/G]TAAACCCGGGAGGCG | 55213 |
rs546888441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569331 | GTAATCCTAGCACTA[C/T]GGGAGCCCAAGCCGG | 55213 |
rs546896593 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556481 | AGGCGTGAGCCACCA[C/T]GCCCAGCCTCATGGA | 55213 |
rs546921533 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579581 | GTGAACCGAGATGGT[A/G]CCACTGCACTCCAGT | 55213 |
rs546947945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571640 | ATTCAGACAAGGTTC[C/T]CTGAGAGGTTTTGTG | 55213 |
rs547154056 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583851 | TGCGCCTGGCCAATA[C/T]GTAACATTTTTAACT | 55213 |
rs547287215 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572159 | TGGTGAAACCCTGCC[C/T]CTACAAAAAATACAG | 55213 |
rs547308103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556601 | ATGTCTAAGCCCCCG[C/T]TCCCCACCCTGCTTC | 55213 |
rs547373718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565331 | GCTCAATGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 55213 |
rs547412317 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585397 | AGCAGGGGCAGGGCC[A/G]AGGGGGAAGAGGCCT | 55213 |
rs547454806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584742 | GACTGCTTTATAAAA[C/T]TGTAATCCCCAGCTG | 55213 |
rs547457032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540814 | GCCTCACGCAAGAAG[C/T]GGGGGAGACGAGCAC | 55213 |
rs547512092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539415 | AGGCTTTTTCTGTAA[A/G]CTTCCTAGGACAGAT | 55213 |
rs547540072 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559484 | ACACGGTGAAACCCT[A/G/T]TCTCTACTAAAAATA | 55213 |
rs547583127 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577832 | GCTTTAAACTACTCA[A/T]AACAGCAACTTCTAA | 55213 |
rs547621350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553825 | GAGAGAAATTTGGCA[A/G]TGGCTATCAGTATTT | 55213 |
rs547742491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566162 | TAGGAAAACCAGAGA[C/T]CTTTGTTCACTTGTT | 55213 |
rs547797079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581002 | TAAAGAGAAGCAGGC[A/G]CCTGCAACAGTGAGC | 55213 |
rs547797751 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585879 | AGATGGCTTGGCTGT[A/G]GGGAGGGTCGGCCTA | 55213 |
rs547860873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571704 | TCCTTAACTTGGGCG[C/T]GTGGCATTTCCCTCC | 55213 |
rs547901882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572201 | GAGTAGTGGCATGCA[C/T]CTGGTGTCCCAGCTA | 55213 |
rs547970026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573302 | CATTTTCTTTCTTTG[A/T]ATTTTTATTCTATTT | 55213 |
rs548185001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559519 | AAATTAGGCGGGTGT[A/G]GTGGTGGGTGCCTGT | 55213 |
rs548235465 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585955 | CCCTGCCCACTCTAG[A/G]GCGCGTCTGGCCCCG | 55213 |
rs548250623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579229 | GGCTGCAAATCACAG[A/G]CAAAGTTTCGAAGAT | 55213 |
rs548295540 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586458 | GCTCCTAGGAATAAA[C/T]AGAAAAACATTTCAT | 55213 |
rs548337407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554432 | GAAGTCATTTCATGA[A/T]ACTGAGATTGATTTT | 55213 |
rs548443975 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549340 | TTTTGACGGAACGTA[C/G/T]GAAAGCTAATAGAGA | 55213 |
rs548606858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581195 | GACCACAGAGACATG[A/G]GACGACAAAGGAGTG | 55213 |
rs548618852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574064 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 55213 |
rs548749456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541511 | GTCCAAAACTATTAA[C/G]CATAATAACTACACA | 55213 |
rs548860412 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536478 | TACATAATCTGTTCC[A/T]TTCATTCTGCAAAGG | 55213 |
rs548915176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567378 | CTGAGCTAACTTTCA[A/G]AAAAAAGACCTGTTA | 55213 |
rs548947024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538019 | GGAAGCAGGTAGTCT[C/T]CATCTTCCTAGCATT | 55213 |
rs548984430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545049 | CATCTATAAACTACC[A/G]AAGAAAACCACCAAA | 55213 |
rs549066908 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557151 | AAAATCTCTGTAACA[C/T]CACTGAGGGACTTCA | 55213 |
rs549069806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582893 | ATAAACAGTGGAGTG[A/G]AGGCCGGGTGTGGTT | 55213 |
rs549076270 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577139 | TTATTTTACTTTATA[C/T]TCTGAAAGCAAATTC | 55213 |
rs549143943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551666 | AGCGCTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 55213 |
rs549147090 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573726 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACCGC | 55213 |
rs549187394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540497 | ACATCCCCAGCTTAT[A/G]ACAGGGCAGAGGTGG | 55213 |
rs549212288 | snp | C/T | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531562 | GAGGCAGAACTCAGG[C/T]AGTAATGCTCACTCA | 55213 |
rs549217247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539044 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 55213 |
rs549238337 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559620 | GAGATCGTGCCACTG[C/T]ACTCCAGCCTGGGCG | 55213 |
rs549247102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558462 | TTTGGGAGGCCGAGG[C/T]GGGAGGATCACCTGA | 55213 |
rs549266478 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545012 | GACAAATCAATTCTA[A/C]GGTATTAAAGTAAGT | 55213 |
rs549280613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577058 | TCAATATCCCATTCC[C/G]TGGGATGGCTTATCC | 55213 |
rs549314240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546749 | TCTAATACCGCTGCT[C/G]ATCTGATGGGAGGTG | 55213 |
rs549333530 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559162 | AATCTATCAATGACA[A/T]TATGTGGGCACTTAC | 55213 |
rs549430240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583411 | GTGTGTGTGTGTGTG[C/T]GTTTTAAATGTGATC | 55213 |
rs549479259 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558556 | AAAATTAGCCAGGCA[-/T]GGTGGCAGGCGCCTG | 55213 |
rs549531152 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565234 | GTTGGCCGGGTTGGT[C/T]TCCAGCTCCTAACCG | 55213 |
rs549551330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577307 | GGAAAGGCTAATTTT[A/G]TTTTAGTTTATTTTA | 55213 |
rs549783002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570830 | TTGTGAGGAGGAGAC[C/T]GTAAACCATTTCTGA | 55213 |
rs549795558 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565603 | GCCCATCGTCTGGGA[A/T]GTGAGGAGCGCCTCT | 55213 |
rs549826860 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533712 | GATGGGGCCTCTCCA[C/T]TCATCTCACAATTCC | 55213 |
rs549887464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545945 | CATTACCTTTCACCT[A/G]AGCCCTGTGACCTTA | 55213 |
rs549978087 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573740 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTTCTTT | 55213 |
rs550033970 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553244 | GGAAAGTGCAATACA[A/T]CTATAAATTTCTCAT | 55213 |
rs550100688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540754 | CAGTTTTCAATGGGT[C/T]CACTGATTCCCTAAA | 55213 |
rs550111475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553669 | CGAGCCCCACAGCAA[G/T]GTAGGGCGGCAGACA | 55213 |
rs550145136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572264 | CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGA | 55213 |
rs550152142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547798 | CACAAGTTGTTTGCT[G/T]TTTTTATTGAGACAG | 55213 |
rs550229100 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586022 | CGGCGGAGCTGGGAC[C/T]AGTTTGTTTTTACTG | 55213 |
rs550286932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559336 | TTACGTGAGGTACCT[A/C]GAGTAATCAAACTCA | 55213 |
rs550316278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49550425 | CTATATTTCTCAGTA[A/G]TATGCTTCTTGGGTA | 55213 |
rs550324087 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559467 | CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 55213 |
rs550348095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544213 | GGTAGCTCACATCTG[C/T]AATGCCAGCACTTTG | 55213 |
rs550384863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537871 | AATCATCAACTTACT[C/T]TTGAAACTCCCTGTA | 55213 |
rs550436437 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579824 | CTCTGATTGTGCCTA[C/T]CCTTTGTTTCATAAG | 55213 |
rs550460457 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585197 | AAAACTTTCCCTCGC[C/T]TCTCCCCATCCTTCC | 55213 |
rs550516171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563324 | TCCACTGTACTCCTG[A/C]CTGGGTGACAGAGAG | 55213 |
rs550518946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585842 | GGAACGCGCGAGGCA[C/T]GGGCTCCTGCTCTGC | 55213 |
rs550729666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562034 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGGG | 55213 |
rs550748718 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532125 | AAAAAATCAATTCAA[A/G]TAAGAGTTGTCATAT | 55213 |
rs550792773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574742 | TCCATTTCTAGCATA[C/T]ACCCCAAAGAACTGA | 55213 |
rs550814042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569374 | AGCCCAGCAGTTTGA[A/G]ACCAGCCTGGGCAAC | 55213 |
rs550822538 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538027 | GTAGTCTCCATCTTC[C/T]TAGCATTTTGGCCCA | 55213 |
rs550851301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557313 | AGACTTGACCAAAGG[C/G]AATGGAAATGGAGAG | 55213 |
rs550860973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551683 | AGGCAGGCAGATCAC[A/G]AGGTCAGGAGATTGA | 55213 |
rs550895595 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545203 | TGGTTCTCTTCTAAG[A/C]CTAAGAATTTGTTTC | 55213 |
rs550905472 | snp | A/C | 0.205417 | 0.245993 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569718 | TGAGAGACCCTGTCT[A/C]AAAAAAAAAAAAGAA | 55213 |
rs551082073 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582594 | TGAATGTGAATGAAA[G/T]CCAGTTTAAAGGTTA | 55213 |
rs551124620 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535900 | TGGTGGCAAGCACCT[A/G]TAATCCCAGCTACTC | 55213 |
rs551323387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543615 | TTAGCTTATGTGCCT[C/T]TTTCTGCAATGGCAA | 55213 |
rs551363537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551132 | GAAGGGAAGGGGGGA[G/T]GGAGAAGGGGGAAGG | 55213 |
rs551405801 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538964 | AACTTCTCCCTCCCA[C/G]ATTCAAGCAATTCTC | 55213 |
rs551467623 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539968 | TGATAAACTCCTTGA[C/T]ACCAGATATTCTGCT | 55213 |
rs551493499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556540 | GAGATGAATTAGGGA[C/G]GGAGGTGTTGGCAGT | 55213 |
rs551530580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557222 | AGAGGACAGCAAAGC[A/C]AGACTGGACAGACGG | 55213 |
rs551531951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538718 | AAGACCCTGTATCAC[C/G]AGGAAAAAAAAATAC | 55213 |
rs551564461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576142 | CAGTGAGCCAAGATT[A/G]CACCACTGCACTCCA | 55213 |
rs551661528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548078 | GCCACCACACCCAGC[C/T]GGTTCTTCACTTTTT | 55213 |
rs551689152 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582860 | GGCTTTTTGCTAAGA[A/G]TAAGAGGGGAGGTAG | 55213 |
rs551724406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575689 | TGGGAACTAAATATA[G/T]GGTACACGTGGATAT | 55213 |
rs551736135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584136 | TGCAGCATACGGGCA[C/T]GCTTTAAAATTTTCA | 55213 |
rs552087591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549697 | ATGATCACAGAAGCC[C/T]ACAGCACACCACACA | 55213 |
rs552262144 | snp | C/G | 9.88435e-05 | 0.00702937 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566708 | GCTTTTTGGGTACAA[C/G]TGTACTCTGGTTATC | 55213 |
rs552315969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549356 | GAAAGCTAATAGAGA[A/G]TAAAACATTCTGAGA | 55213 |
rs552350807 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542162 | GAGGTTGTGGCGAGC[C/T]GAGATTGCGCTTCTG | 55213 |
rs552429062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574629 | ATAAAATTAAATGTA[G/T]ATGGTAGAAATGTAA | 55213 |
rs552430570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542658 | TATTGTCTGATTATC[C/T]GACAATTTTTCTTCT | 55213 |
rs552521937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548850 | TTTCTTCTGGGGTGA[C/T]TAAAACAATTTAGAA | 55213 |
rs552581795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536688 | TCCTCTTATAGCCCA[C/T]GGAATAGGGAAGTGG | 55213 |
rs552586149 | in-del | -/AA | 0.40733 | 0.194287 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569718 | GAGAGACCCTGTCTC[-/AA]AAAAAAAAAAAAGAA | 55213 |
rs552596549 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570749 | ACTATCCTGAACCTG[C/T]CTTGTCGTAGACACT | 55213 |
rs552685931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548162 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG | 55213 |
rs552700982 | snp | A/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586416 | CATAGCATTCCAGCC[A/T]CTTGTTCACTTACCT | 55213 |
rs552745879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536084 | TGGTGCCACTAATCA[C/T]AATTCACTTTATACA | 55213 |
rs552760748 | snp | A/G | 1.66657e-05 | 0.00288662 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567314 | TCCTATAAATAAGCC[A/G]ACATCTCTGCTGGAA | 55213 |
rs552812777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568191 | TACTTAACAGTACAT[C/T]GGGGAAATCATTCTA | 55213 |
rs552855127 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573159 | AATAAATGTACCCTG[A/T]AAGACTTAGTTAGCT | 55213 |
rs552913242 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581588 | CTGGCATGAAATCAC[C/T]CAGGAAAAAAGCAAG | 55213 |
rs552919640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561524 | TGAAAGAAATGTCCA[A/G]ACTAATGAGTGTTTT | 55213 |
rs552942778 | snp | A/C/T | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541735 | TACTGGAGAAAGGCA[A/C/T]GATACACTGGGTAAG | 55213 |
rs552947698 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586864 | TTTTTACCACTTCAA[C/T]TACTGTTTGGCTCTG | 55213 |
rs552960574 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570699 | CCTAGCAAGACAATC[A/G]AGCAAAGCTAACAGC | 55213 |
rs552975657 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586119 | CTAGGGAAGGTGGCA[C/G]CTGGACAAAGGTATG | 55213 |
rs553033344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567686 | AGCACACACAGAGGG[C/T]GCCTGCAGCTGGAGC | 55213 |
rs553049990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561616 | AAAATTCAGTATCAT[A/G]AAGATTCTAGTTTTT | 55213 |
rs553116619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555238 | TTACATTAAATATCA[C/T]GAACAAATAGCTATA | 55213 |
rs553156548 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535087 | CTCTCCTAATAATGA[C/T]TTTATTTTTAAAGCC | 55213 |
rs553202237 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49580538 | GGCTGCAGTGAGCCG[G/T]GTTCACACCACTGTA | 55213 |
rs553246726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557700 | TGAGACAGGAGGATC[A/G]CTTGAGCCCAGGAGT | 55213 |
rs553294227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555279 | TCTTTGGATCTTGCA[A/G]AAAATACAACTTAGA | 55213 |
rs553452033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560912 | GGGATGAGGGGTGCA[A/C]GGAGCTCCCATGCCC | 55213 |
rs553474868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570867 | AGGACTGAGGCTCAA[A/G]GGTGAAATGACGCCA | 55213 |
rs553514929 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587511 | TATTCCAGTACAGGG[G/T]GAAAAGTATTATGAT | 55213 |
rs553541689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537139 | GTGAGCAGGTGCCTC[A/G]GCATCACAGCTCCCC | 55213 |
rs553562140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581901 | TGTGGGTGGAAGAGG[C/T]CAGGTTGCAGCAGGT | 55213 |
rs553577551 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550787 | TCAACCTCATGTTCA[C/T]TCTGGCTACTACTCA | 55213 |
rs553614349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543775 | ACCACAGCCTTGATC[C/T]ACTGGGCTCAAGCAA | 55213 |
rs553717779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584449 | TACAGTTACATCCTC[C/G]ACCCTGAAAGCAGTT | 55213 |
rs553760238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558086 | AAAATGTCAATTCCC[A/G]GCCAGGGCCACTGTC | 55213 |
rs553899828 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578198 | TTGCACATAACCTAC[A/G]CACATCCTCCCATAT | 55213 |
rs553981125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546512 | ATTGTGCACTTAATT[C/T]TTATTATTGTTACAC | 55213 |
rs554016020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546964 | AACTTAACATTTAAA[C/T]TGTTAGGACATTTGT | 55213 |
rs554020308 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560028 | CAATGCCTTGGTTGG[C/T]CGTCCCATTCCCAAG | 55213 |
rs554120069 | in-del | -/CACCCTTGC | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547263 | TCACTTTAAGGCAAG[-/CACCCTTGC]CTTAACTCTTCCTAA | 55213 |
rs554152796 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565743 | GCCCCTCTGCCCGGC[C/T]GCCACCCCGTCTGGG | 55213 |
rs554209284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584950 | AAAGTCCTCACTAAC[A/C]AAATCCCTGCCTTTG | 55213 |
rs554222724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565018 | CCGCTCCCATTCCCA[C/T]TCCCGCTCCCTCTCC | 55213 |
rs554252538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571757 | AAATACCACCAAAAC[G/T]TTCTAATTTACTCAA | 55213 |
rs554259909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565427 | ATTGCAGCCTCTGCC[C/T]GGCCGCCACCCCGTC | 55213 |
rs554286821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539852 | CTCAAACAAAAATAA[A/G]ATACATTTTGAAAAC | 55213 |
rs554305064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559580 | AAAATGGCGTAAACC[C/T]GGGAGGCGGAGCTTG | 55213 |
rs554326885 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561328 | GAAGACAGCCCACAC[A/G]AACTCAGAGTCCTCT | 55213 |
rs554333440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585025 | GACAGCACTACTCTC[A/G]GGAGACGAAGGAGAG | 55213 |
rs554390267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585438 | GACCCCGCGCCCACA[C/T]GCTACCTGCGAGGTC | 55213 |
rs554427800 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541937 | GAAGTATCCTTGGGC[C/T]GGGCGTGGTGGCTCA | 55213 |
rs554466825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566389 | TCATCCACAGCTTTA[C/T]GGAGGCAGTCGAAAA | 55213 |
rs554467642 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534514 | AACACACACGCGCGC[A/G]CACACACACACACAC | 55213 |
rs554496394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578932 | AATAAGAGAGCTCTA[C/T]GGTTTGGGGTAAACT | 55213 |
rs554503240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559389 | TGGCTGGGCACGGTG[G/T]CTCACGCCTGTAATC | 55213 |
rs554642975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535553 | TTTCCAGCTACCACG[A/C]GGTGGGAATGTTAGA | 55213 |
rs554656253 | in-del | -/TTT | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557767 | CTCTACAAAAAAAAA[-/TTT]TTTTTTTAAAAGAAT | 55213 |
rs554706434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573021 | CTCTCTTCCTTCCCA[C/T]GGTGCTATGGTTTGT | 55213 |
rs554778514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548051 | CCCAAAGTGCTGAGA[C/T]TACAGGTGTGAGCCA | 55213 |
rs554838595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553394 | GCAAATAGGTGAGCT[C/T]TGATGAGGCTCTAAA | 55213 |
rs554938890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547056 | GTCCAGGTTAAGTAG[C/T]ATATACAAATCTGAA | 55213 |
rs554979326 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575162 | GAAAAAATATTCAAC[A/T]TCACTAATCATCAGA | 55213 |
rs555026426 | in-del | -/AAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543697 | AAGGAACTATATCTT[-/AAA]AACTTTTTTTTTCAT | 55213 |
rs555041023 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531674 | CCCTGACCTAAAGGA[C/T]TCTTCATCTTGGAAA | 55213 |
rs555044741 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566410 | CAGTCGAAAACCTCA[C/G]AAGTTTGCCTAATTT | 55213 |
rs555050445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572465 | CTAACTATGGATTTC[A/C]TTTCAAAGGAATATA | 55213 |
rs555097363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554609 | GCAAGGGAGTATTAC[C/T]GCCTGAGCGCCACCT | 55213 |
rs555114210 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564618 | AAAAAAATGCCGGGC[A/G]CGGTGGCTCACGCCT | 55213 |
rs555182313 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532070 | TTTAGGGCTATCTTA[A/G]GAAATATGAATACTT | 55213 |
rs555245011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551113 | CAAAAAAGGGAAGGG[A/G]AGGGAAGGGAAGGGG | 55213 |
rs555277661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559621 | AGATCGTGCCACTGT[A/G]CTCCAGCCTGGGCGA | 55213 |
rs555387209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575728 | GAACAACAGACACTG[G/T]AGACTACTACAGGGG | 55213 |
rs555477608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544657 | TACTACCAAGGCTAT[C/T]TTTTATCAGTACTCA | 55213 |
rs555486104 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539031 | CGCACCACCACACCC[A/G]GCTAATTTTTGTATT | 55213 |
rs555595957 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559969 | GCCACAAGCTACTTC[C/T]ACCACTTGCTTGATC | 55213 |
rs555612745 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550633 | AAGTTTATATTACAC[C/T]ATAAACATCAACATG | 55213 |
rs555683323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569439 | AAAAAAGGCCAGGCA[C/T]GGTAGCTCACTCCTG | 55213 |
rs555746551 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584822 | ACAAAAGGCCACTTA[C/T]GCGAGCAGAACACAG | 55213 |
rs555752030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576553 | TTTATAAAAGAAATA[C/T]AGCCTTCTTAGAATT | 55213 |
rs555771922 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535158 | CTCAGAACATCACCC[A/C]CACAGAAGTATATTT | 55213 |
rs555828902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557802 | ATTCTACTGCCATCA[A/G]AAGTGTAATCTTGAT | 55213 |
rs555993145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584244 | ATCATTTGGATCACA[C/T]ACTTAAAAAAATCAC | 55213 |
rs556031757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577706 | CATGAAATGAGTTTG[C/T]GTCATTCTTTATTAT | 55213 |
rs556039611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552085 | AGAGTATTGCCAGAA[A/G]AGACTGACTGAAGAG | 55213 |
rs556103432 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539110 | CCTGATCTCAAGTGG[C/T]CCACCTTGGCCTCCC | 55213 |
rs556217301 | in-del | -/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587269 | GAATTTACTAGAAGA[-/G]GCCTGTTTTGCTCAA | 55213 |
rs556233258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563562 | TACTTCGGAGGCTGA[A/G]GCATGAGAATTGCTT | 55213 |
rs556374554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545639 | TGTATGAAAGAAGAA[A/C]AGAAGCAGAAAAGGG | 55213 |
rs556458597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543950 | CCTTGGCCTCCCAAA[A/G]TCCTAGGATTACAGG | 55213 |
rs556473139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564488 | CTACTCGGGAGGTTG[A/C]GGCAGAAGAATCGCT | 55213 |
rs556487149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534488 | CTCTAACTCAAAGTA[C/T]GACTCTTCAAAACAC | 55213 |
rs556503346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542322 | ATGCAAGTGGTTTTT[A/G]TACATGCCTTTTACA | 55213 |
rs556516062 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557896 | GGGCTACAATATTCA[C/T]ACCACATCAAGTACA | 55213 |
rs556540164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536335 | ACGTTTGAATTTGCA[A/G]GTTCACCAGAGAGTC | 55213 |
rs556543483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571113 | GCACTTTGAGAGGCC[A/G]AGGCGGGCGGACCAC | 55213 |
rs556585666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584342 | AAAGGACCCGTCTAG[A/C]GTATTAATAAATAGA | 55213 |
rs556629637 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543490 | CAGATATTTACTCCC[G/T]TAGGTAAGGAATGAC | 55213 |
rs556664001 | snp | A/G | 4.95593e-05 | 0.00497767 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541798 | TCTTCATTCCAATAC[A/G]ACTGGAACATGGATC | 55213 |
rs556780389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568344 | AGAACAATAGTGCAA[C/T]TGTTGCCTGCACATT | 55213 |
rs556859010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578706 | AACAGAAAACAATTA[C/G]ACGAAATCCCAGAAA | 55213 |
rs556861696 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572630 | CAACATGGCAAAACC[-/CT]GTCTCCACTAAAAAT | 55213 |
rs556944533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581367 | CAGAAAGGCAGAGCC[A/G]AAGATCACAGGCAGA | 55213 |
rs557008596 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548935 | GTCAGGAGTTCGAGA[A/C]CAGCCTGGCCAACAT | 55213 |
rs557025157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556784 | CAAAGTATATTCACA[C/T]AAATATCTAGTTTAA | 55213 |
rs557066947 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586195 | AGAGGTACCTCGGAA[A/G]CATGCCATAGAGGTT | 55213 |
rs557080365 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554549 | GGCCGGTACCAGTCC[A/G]TGCCCTGTTAGGAAC | 55213 |
rs557121796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582411 | AGAATCGCTTGAACT[C/T]GGGAGACGGAGGTTG | 55213 |
rs557184836 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573729 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 55213 |
rs557284862 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566520 | TAAGAAGCAAACAAT[A/C]CAAAATCAGTTATCT | 55213 |
rs557330869 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551143 | GGGAGGGAGAAGGGG[A/G]AAGGGGGAAGCAGGG | 55213 |
rs557493212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544424 | CGGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 55213 |
rs557559573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550068 | GACCATGGCTCACTG[C/T]AGCCTCGACCTCCCA | 55213 |
rs557589548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538259 | TCAGCATCCTGAGTA[C/G]CTAGAATACAGGCAT | 55213 |
rs557590541 | snp | A/G | 3.4462e-05 | 0.00415088 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541646 | TATTCTCCACCATGC[A/G]GCTCGTCCATCCCAA | 55213 |
rs557628962 | snp | C/G | 0.43221 | 0.171171 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562775 | GTGCCACCATCCCCG[C/G]CTTTTTTTTTTTTTT | 55213 |
rs557660389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551197 | GGAGAAGGGAAGGTT[A/G]TCTCTTTTGTCCAAA | 55213 |
rs557714222 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543808 | CTTCCACCTCAGCCT[A/C]CAGAGCAGCTGGAAC | 55213 |
rs557827335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542430 | CACTACTGTTTCCAT[C/T]TGATGGTCCCCAAGA | 55213 |
rs557834477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574315 | GTAGAGACGGGGTTT[C/T]ACCATGTTAGCCAGG | 55213 |
rs557874820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544567 | TAAAACGCTCCATGA[A/G]TGTACACAAAAAACT | 55213 |
rs558001254 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583006 | ACATAGGGAGACCCT[A/G]TCTCTACAAAAAATA | 55213 |
rs558020394 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568423 | CTAAAAATGAAAATT[A/G]CTAGGTCAAAGTCTA | 55213 |
rs558025787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577858 | TCTAATATGCAAAAT[A/G]ATATTTTTAATTGCA | 55213 |
rs558086837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554061 | AATGATGGAAAGCCG[C/T]ATAAATGGTCTGATC | 55213 |
rs558298765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538973 | CTCCCAGATTCAAGC[A/G]ATTCTCCTGCCTCAG | 55213 |
rs558380065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580349 | CAGCATTTTAGGAGG[C/T]GAAGGCAGGAGGATC | 55213 |
rs558382869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571733 | CCTAAGGCAGCAGAG[C/T]GTAACTGTAAATACC | 55213 |
rs558400100 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543029 | TGGGAGGCCGAGGCA[G/T]GTCAGCCTCAATCAC | 55213 |
rs558432755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541606 | GAAGCTTTTTACATT[C/T]CAGGACTAAGAATAT | 55213 |
rs558437957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583543 | TTCTTCAGCACGTAC[A/C]CAACATGTACTTTTT | 55213 |
rs558439811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579530 | TCTGGAGGCTGAGGC[A/T]GGAGAATGGCGTGAG | 55213 |
rs558441280 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586074 | CCGCCCCTCACTTCC[G/T]GATTGAAAGTACCTG | 55213 |
rs558458736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545509 | AAGAACACAGGATCA[C/T]CTTACCTGATAAGAA | 55213 |
rs558468709 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547855 | GTGCAGTGGTGCGAC[C/T]ACAGTTCACTGCAGC | 55213 |
rs558667898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584869 | CTTAAACCGAGCAGG[C/T]AGGTACTTTATCAGA | 55213 |
rs558705020 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547975 | GTAGAGATGGGGTTT[C/T]GCCATGTTGCCCAGG | 55213 |
rs558756781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534995 | GCCGAGATCGCACCA[C/T]TGCACTCTAGCCTGG | 55213 |
rs558761879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562916 | AGGCATGAGCCACCA[C/T]ACACAGCCAACAAGG | 55213 |
rs558784581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573606 | GGCGCCCACCATCAC[A/G]CCCGGCTAATTTTGC | 55213 |
rs558841970 | snp | A/G | 9.88973e-05 | 0.00703128 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540910 | GCAGCAGAGAATAGC[A/G]AAAAGGCATTCTCCA | 55213 |
rs558915946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579160 | AGAATCAGCCTCAAA[C/T]ATTTTTAAATAAAAA | 55213 |
rs558925265 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546828 | GAAGCTTCGCTCACT[C/G]CCACTCACCTCCTGC | 55213 |
rs558952134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560154 | ACTTTCTTCCCCAGA[A/T]CTTCGTACAGCTCCT | 55213 |
rs559020374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547369 | GTTTTAGAAAATTAA[A/C]CTTCAATATCAATTG | 55213 |
rs559066851 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585515 | CCAATGGGCGCAGAA[A/G]TGCGAGCGAGCGGCG | 55213 |
rs559067685 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564441 | AGTACAAAAATTAGC[C/T]GGGGCGTGGTGGCAC | 55213 |
rs559112423 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584566 | TTTTTCCATTCCTTC[C/T]GGCATTATATACTTT | 55213 |
rs559150323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556025 | CATTCCCTCTATAAT[C/T]TGTGTGTGTGTGTAT | 55213 |
rs559159769 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535910 | CACCTGTAATCCCAG[C/G]TACTCAGGAAGCTGA | 55213 |
rs559169502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567041 | CATAGTCTTCCTGAA[C/T]TTCAGGATCTCTTTA | 55213 |
rs559230856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566579 | AATTAACCGGTCAAT[G/T]TCTTACAAACTGAAA | 55213 |
rs559266568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534662 | TTCAAGACATCAGAG[A/G]AAAGAATTAAGATGT | 55213 |
rs559355415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585166 | CGTGCACCTCAAAAA[A/G]GAGAGGGAGGCAGGG | 55213 |
rs559434375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540461 | ATAGAATTGCAGAGC[A/G]TACACAGATACAAAT | 55213 |
rs559536186 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532027 | CTAGAGTATCAAACA[C/T]TGTTCCAGTAAGAAG | 55213 |
rs559546868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559733 | GTTTACCAGGGACAG[C/T]GTTTCAGTTTTGCAG | 55213 |
rs559619181 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581887 | AGTTTCACTGAGGTT[A/G]TGGGTGGAAGAGGCC | 55213 |
rs559706184 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586399 | AAATCCAAACTTGTT[A/G]GCATAGCATTCCAGC | 55213 |
rs559744657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549213 | CTTTACAATGGTTAA[C/T]TGCATGTTATGCGAA | 55213 |
rs559789111 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577850 | CAGCAACTTCTAATA[C/T]GCAAAATGATATTTT | 55213 |
rs559920804 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533545 | TATACGTTAAACTTA[A/T]TACTTTGATTTATCT | 55213 |
rs559951079 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581102 | GGCTTTATCCTAAGA[A/G]CACCAGGTAATCCCT | 55213 |
rs560020002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574020 | AACTCCTGACCTCAA[A/G]TGATCCACCCACCTG | 55213 |
rs560089008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542105 | TATAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA | 55213 |
rs560123958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542467 | TGCTCCTTTGTTTTT[C/T]TTAAAATGATGTACA | 55213 |
rs560147521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551638 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55213 |
rs560201174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575199 | CAAATCAAAACCACA[A/G]TGAGATACTATCTCA | 55213 |
rs560203022 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557085 | CCAGTCATGAAATCT[C/T]GGTCTCCCTGAGCTT | 55213 |
rs560241272 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573694 | ACCTCAAGTGATCCA[C/T]CTACCTCGGCCTCCC | 55213 |
rs560256142 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533957 | GGGCTCAAGAAAAGC[C/T]GTACACCCTTGTTAT | 55213 |
rs560289935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583839 | GATGTAAGCCACTGC[A/G]CCTGGCCAATATGTA | 55213 |
rs560308787 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557647 | ACTCTAGGTTGGGTG[C/T]GGTAGCTCACACCTA | 55213 |
rs560388822 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584662 | GCTTTTAGTCCTCCC[-/A]AAAAAAAGAATAGGG | 55213 |
rs560421156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576874 | ATAAAGATAAAACAA[A/G]GGTGCAAGGAAAGAA | 55213 |
rs560463163 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560804 | TTGTCACTCACACTG[C/T]TGTGACTATCTCTGG | 55213 |
rs560639466 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539250 | CATGCATTTTTGAGC[A/G]CCAGCTCCATGCCCA | 55213 |
rs560646440 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550306 | AATGTAACTTTTTCT[C/T]TCATCTCCTACCAGA | 55213 |
rs560679693 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562102 | GACTCTATCTCAAAG[-/A]AAAAAAAAAAAAGGT | 55213 |
rs560690142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538846 | TCTCTAATTTTTCTA[C/T]GTTGAATCTGTAATA | 55213 |
rs560730618 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534991 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCTAGC | 55213 |
rs560796625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551672 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACAAGGT | 55213 |
rs560964556 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548591 | GACAAACAAAATATG[-/GT]GTATATATATATAAT | 55213 |
rs560978791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577085 | ATCCTAGCTATTGGC[A/C]CTGTCCCTCAGAGAA | 55213 |
rs561053842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552345 | GTAAGAAGGAAGAGA[C/T]AAAAAAACCAGCCCA | 55213 |
rs561092428 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533530 | TTTCAACAGGTTTAA[C/T]ATACGTTAAACTTAT | 55213 |
rs561098593 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540524 | GTGGAAAGACAGCAA[C/G]GTAAGTCTCGAAATA | 55213 |
rs561111206 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534051 | AGAATCACATCACCC[A/G]TAGAGCACAAACTGG | 55213 |
rs561125642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577994 | GCTAAGCTGTCTTAC[A/G]AAAAAAATTTATTTA | 55213 |
rs561188971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584506 | CACTTGAAATGAGTA[C/T]TCTAAAGTTTAAAGC | 55213 |
rs561192156 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571779 | TTTACTCAAAATTAC[C/G]ACCATCCTCATTATA | 55213 |
rs561232607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559166 | TATCAATGACATTAT[A/G]TGGGCACTTACTATA | 55213 |
rs561260479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547466 | CACTTATTCCCTCTG[C/T]TTATAAATAAAACAA | 55213 |
rs561276687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566891 | GAAAAGAGACTGATA[C/T]GGTTGTTAAGAAAAA | 55213 |
rs561277755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548287 | ATCCCAGCTACTCAG[A/G]AGGCTAAGGCAGGAG | 55213 |
rs561330177 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565240 | CGGGTTGGTCTCCAG[C/T]TCCTAACCGCGAGTG | 55213 |
rs561373040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565780 | ACCCAACAGCTCATT[A/G]AGAACAGGCCATGAT | 55213 |
rs561384864 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546869 | AGTTAATAACAGGCC[A/G]CGGACCAGTACAGGC | 55213 |
rs561435790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554200 | TAATTATACTCACCC[A/C]TATATAATTGTTTAA | 55213 |
rs561443168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585178 | AAAAGAGAGGGAGGC[A/C]GGGAAAACTTTCCCT | 55213 |
rs561477660 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585633 | GCGCGCGCCCGGGAC[A/G]CTACCCAGCCGAGCA | 55213 |
rs561602847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553648 | ACCCAAGATTTGTGG[C/T]GGCATCGAGCCCCAC | 55213 |
rs561624365 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536182 | TGGGTATGCAATAAA[C/T]ATTCAAAAGTTCCAA | 55213 |
rs561662084 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550392 | GTTCCAATCCAAAAG[A/G]AAAACAAGCCAAACT | 55213 |
rs561733375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568057 | TCTCCTCAAAGGCCA[A/C]CACTGTTCCCAGTGA | 55213 |
rs561735487 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573691 | CCGACCTCAAGTGAT[-/C]CACCTACCTCGGCCT | 55213 |
rs561813559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556430 | CTCCTGACCACGTGG[C/T]CCACCCATCTCGGCC | 55213 |
rs561896667 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532033 | TATCAAACATTGTTC[C/T]AGTAAGAAGTTCAAG | 55213 |
rs561927521 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575425 | CCAAAGGAAAATAAA[C/T]TGTTCTACCAAAAAA | 55213 |
rs561986111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564617 | AAAAAAAATGCCGGG[C/T]GCGGTGGCTCACGCC | 55213 |
rs562049278 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563709 | CAGAAGGCATGATTA[C/T]GCAAGGCAAAAGTGA | 55213 |
rs562077683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537820 | TTAATAAAACTTGTG[G/T]ACAGTTTCATAACAC | 55213 |
rs562088549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538498 | GGAGGGACACTTGAG[C/T]CCAGAAGTTCAAGAC | 55213 |
rs562105207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583075 | CCAGCTACTTGGGAG[A/T]GGGGAGGATCACTTG | 55213 |
rs562115260 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532674 | CACTCCCCTTCCCAC[A/C]CCAATAGACACAAAT | 55213 |
rs562141285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575946 | TAATCCCAGCATTCT[C/G]GGAGGCCAAGACGAG | 55213 |
rs562282237 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571069 | AAAAGTATCCAGGCC[A/G]GGCGGGGTAGCTCAC | 55213 |
rs562283017 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569291 | AAAGTTTAAAAATAA[A/G]GGCTGGGCGCAGTAG | 55213 |
rs562515736 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533492 | TTGACTAACCTAGAA[A/T]ATTTATCTTTACATA | 55213 |
rs562528885 | in-del | -/AAAG | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569728 | TGTCTCAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 55213 |
rs562572983 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563111 | TCACATACAAAATAG[A/C]AAAAGTTGCCAGGCA | 55213 |
rs562573394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556470 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC | 55213 |
rs562633564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538638 | GGAGGACTACTTGAG[C/T]CCAGGAAGTTGAGGC | 55213 |
rs562651336 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545332 | CTTAAATGGTAATGC[C/T]AAGCGGTCATGTTCT | 55213 |
rs562655637 | snp | C/G | 1.66109e-05 | 0.00288187 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544750 | ACCTGATTTTCAAAA[C/G]AGCTTTATGGACATG | 55213 |
rs562671130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582685 | CTCCATTTTACATGC[C/T]CACCGGCAATGTACA | 55213 |
rs562671926 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585099 | GGGAGATCTCCTCTC[A/C]GTAAAACGGCACCCA | 55213 |
rs562676216 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532840 | TCAAATGGAAATGAG[C/T]TCATGGACCAGAGAG | 55213 |
rs562680387 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558722 | AAAAAAAAAAATTCA[C/G]AAAGTAGACAATAAC | 55213 |
rs562699496 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542133 | GCAGGAGAATCGCTT[C/G]AACCCGGGAGGTGGA | 55213 |
rs562709877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583129 | TGAGCTATGATCACA[C/T]GGCACACTGTACTCC | 55213 |
rs562752389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557588 | CACACATCTGAGCTA[C/T]AGTCTTAGCAAAGAG | 55213 |
rs562816373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576051 | AATTAGCCGGGTGTG[A/G]TGGCGGGCACCAGTA | 55213 |
rs562864346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | RCBTB1 | GRCh38.p7 | 13:49558328 | TGTGGCCACATGCAA[C/T]CCTGAACTGGAACAA | 55213 |
rs562918949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535796 | TTGGGAGGCTGATGC[A/G]GGCAGATCACGAGGT | 55213 |
rs562948874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570315 | TGATGGGGCATTATT[A/G]TACGCACTGACTTCA | 55213 |
rs562972222 | snp | A/G/T | 9.88621e-05 | 0.0070301 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566658 | TCCACTCCCGTAACT[A/G/T]AGGCTTTTAATCTTC | 55213 |
rs563011506 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576700 | CATCTTTAAATAGTT[A/C]CTTCTGAAGTACCTC | 55213 |
rs563035910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578709 | AGAAAACAATTACAC[A/G]AAATCCCAGAAACCA | 55213 |
rs563041278 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532240 | TCTCTTCACTGCCAC[A/G]CATATTCATACAAAT | 55213 |
rs563042907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565139 | CCTGCCTCAGCCTGC[C/T]GAGTGCCTGCGATTG | 55213 |
rs563127126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580706 | TGAATCTTTCTCATG[C/T]GGATACCCCAAAAGT | 55213 |
rs563235101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553364 | ACCTTTAGGAGGTCA[C/T]TTCTTCCCTCGTTAG | 55213 |
rs563242983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560263 | GGTGACAGAACGGGA[G/T]AGACAGATGCAAAAT | 55213 |
rs563281642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572705 | GCTACTCAGGAGGCT[C/G]AGGTGGGAGGATCAT | 55213 |
rs563347198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579809 | TAGTGTTTTAGAATT[A/C]TCTGATTGTGCCTAC | 55213 |
rs563540982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554758 | TGAGGTGGAACAGTT[G/T]CATCCCAAAACCATG | 55213 |
rs563627960 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542546 | CAAAACTTTTGACTA[C/T]GTATCAACATTAAAA | 55213 |
rs563725059 | in-del | -/T | 0.486 | 0.0824865 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573787 | TCCCAAATTTCTCTC[-/T]TTTTTTTTTTTTTTG | 55213 |
rs563757484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568571 | CACAGCGTACTCTCA[C/T]GGCATTTCAGTTTTG | 55213 |
rs563783693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549347 | GGAACGTATGAAAGC[A/T]AATAGAGAATAAAAC | 55213 |
rs563895234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549802 | CAGCAACAAAAGCAA[C/G]AGATCAGGGCAAGAG | 55213 |
rs563962179 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536506 | AGGATCAAATCTTCA[A/G]TAACAGGCAAGAAAA | 55213 |
rs563981588 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574124 | CCAAATTTCTTTTTT[G/T]GGGGGTGGGGGGTGG | 55213 |
rs564135404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582016 | AAATCGCATAGTAAT[C/T]ACAGAATGTGATAGA | 55213 |
rs564172281 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582521 | AATAAATGCAAGAGA[A/C]ACTGTAGAAAGGAGC | 55213 |
rs564174073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574640 | TGTAGATGGTAGAAA[C/T]GTAAGATGATACAGC | 55213 |
rs564211852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561105 | CCACAGCACCCCCGA[A/G]TGCCAAGGGCAGGTC | 55213 |
rs564403672 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576013 | AACACGGTGAAACCT[C/T]GTCTCTACTAAAAAT | 55213 |
rs564430389 | snp | G/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561900 | AGTTCAAGACCAGAC[G/T]GGCCAACACAGTGAA | 55213 |
rs564506103 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584603 | TTAATGTTATTAGCC[-/CA]CAATACACACCAGTT | 55213 |
rs564573909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585094 | CGGAGGGGAGATCTC[C/T]TCTCAGTAAAACGGC | 55213 |
rs564597080 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571293 | GGAGGTTGCAGTGAA[A/C]CGAGATTGCACCACT | 55213 |
rs564631131 | snp | C/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587438 | ACTTGGAGCATCTTG[C/G]AGGATTAAAAGCTGA | 55213 |
rs564633270 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569311 | GGGCGCAGTAGCTCA[C/T]GCCTGTAATCCTAGC | 55213 |
rs564692860 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565062 | GTCTCCCTCTGATGC[C/T]GAGCCGAAGCTGGAC | 55213 |
rs564737626 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558221 | ATGTCTCAATGATTC[C/T]AGTGAGAGTGAGTGT | 55213 |
rs564746901 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569640 | AGAATCACTTGAGCC[A/C]GGGAGGCAGAGGTGG | 55213 |
rs564862589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537250 | AAACCCCAAAACTGT[C/T]AGTCTATAATTCATG | 55213 |
rs564950787 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533597 | CGCAAGCACACAAAC[A/C]AAAGTCTGAAACAAT | 55213 |
rs564973113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553052 | CTGGGCGTGGTGGCG[C/T]GTGCCTGTAACCCCA | 55213 |
rs564980422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572559 | GTAATCCCAGCACTT[C/T]TGGGAGGCTGAGGCA | 55213 |
rs564989288 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535251 | CACAAGGGGTAAACC[A/G]GAACCATTTCAAAAT | 55213 |
rs565009501 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546668 | GGCATTAGATTCTCA[G/T]AAGGAGCTCGCAACC | 55213 |
rs565087788 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559561 | CTTGGGAGGCTGAGG[C/T]AGGAAAATGGCGTAA | 55213 |
rs565144272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535860 | AAACCCCGTCTCTAC[G/T]AAAAATACAAAAATT | 55213 |
rs565170062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540230 | TATAGGGTATACAGA[C/T]GAATGAGACAGTTCC | 55213 |
rs565221016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566459 | TTTCCAGAGTTAGCC[C/T]GAAGTGTTTAACTTT | 55213 |
rs565239820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554284 | ATTCACTTTTTATTT[C/T]ATCTGTTTCACTTGT | 55213 |
rs565306431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541986 | TTTGGGAGGCCAAGC[A/G]GGTAGATCACCTGAG | 55213 |
rs565314776 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586294 | GAGGGACTGCTACGA[A/G]CTGCTCCAGCCTATC | 55213 |
rs565392862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578310 | GGGAATAATGACAAG[A/G]AAAAATACTCTACAT | 55213 |
rs565574572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554649 | TCAATGGCAGCATAA[A/G]ATTCTCACAGGAGCA | 55213 |
rs565602584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541342 | TTAATACCTAGGTGA[C/T]GGGTTGACAGGTACA | 55213 |
rs565838978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559512 | ATACAAAAAATTAGG[A/C]GGGTGTGGTGGTGGG | 55213 |
rs565896932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541476 | ACATTAGAACAAAAA[A/G]GCCTATGGTCATAAA | 55213 |
rs565922510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553924 | ACAAAGATACACATA[C/T]ACAGAGTAACATAGA | 55213 |
rs565936157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585888 | GGCTGTGGGGAGGGT[C/T]GGCCTACCACCCCAG | 55213 |
rs565942371 | in-del | -/T | 0.466927 | 0.124269 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556197 | TTTGTTTTGCTTTGG[-/T]TTTTTTTTTTTTTTT | 55213 |
rs565956394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580053 | GCTCGAAAAGCAAAC[A/G]AACCAAGTGGCAATA | 55213 |
rs566041985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579432 | ATCAAGACCATCCTG[A/G]CTAACACAGCGAAAC | 55213 |
rs566154866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547947 | CAGGCACCACCACTC[A/C]TGGTTATTTTTTGTA | 55213 |
rs566205294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585351 | GTACAGGAGTAACGG[G/T]GCACTCCCGGCCCGG | 55213 |
rs566231171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535484 | TGAAGGTCAGCACTC[C/T]GGGTTCTATCGAACC | 55213 |
rs566242009 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565826 | GTCGAATAGAAAAGG[C/G]GGAAATGTGGGGAAA | 55213 |
rs566268853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566887 | AGGTGAAAAGAGACT[A/G]ATATGGTTGTTAAGA | 55213 |
rs566278856 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564457 | GGGGCGTGGTGGCAC[A/G]CGTCTGTGGTCTCAG | 55213 |
rs566330254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572983 | CAAGTACCTTGGTAA[G/T]TACCCTGAGCAAGGT | 55213 |
rs566457601 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532323 | TAAATATTTGTTGAA[C/T]GAATGAACTATCTAT | 55213 |
rs566481387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582867 | TGCTAAGAGTAAGAG[G/T]GGAGGTAGCAATAAA | 55213 |
rs566495355 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554306 | TTCACTTGTCTTCCT[C/T]TACTTTGTTAAAATA | 55213 |
rs566559141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550653 | ACATCAACATGGCCA[C/T]AGACCTTACTTGTCT | 55213 |
rs566575154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551832 | GTGAACTCGGGAGGC[A/G]GAGCTTGCAGAGAGC | 55213 |
rs566595435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551142 | GGGGAGGGAGAAGGG[A/G]GAAGGGGGAAGCAGG | 55213 |
rs566618639 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574194 | CACCATCTTGGCTCA[C/T]TGCAACCTCCACCTC | 55213 |
rs566644665 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559294 | AGATAAACCAGTTAC[-/A]AAAGGACAAACATTG | 55213 |
rs566650639 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555243 | TTAAATATCACGAAC[A/G]AATAGCTATAGGCAT | 55213 |
rs566684395 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576783 | TTCTGAAAAACAATA[G/T]TAATGTGTTGCAGCC | 55213 |
rs566728155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575697 | AAATATAGGGTACAC[A/G]TGGATATAAAGACAG | 55213 |
rs566739360 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577521 | TATTTGTTTGGGCTA[C/G]TTTAAATTGCTGTTA | 55213 |
rs566755698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538009 | AAGAAACATTGGAAG[C/T]AGGTAGTCTCCATCT | 55213 |
rs566811137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545510 | AGAACACAGGATCAC[C/T]TTACCTGATAAGAAG | 55213 |
rs566843790 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537099 | ACTAGTTGAATGTTA[A/G]TAATTTGAAGACCAC | 55213 |
rs566848283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546189 | CAACTTCTGCATCCA[C/G]TCTTAGGCTGAAATG | 55213 |
rs566888916 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546919 | GACCCCTGATCTAGG[A/C]GGATATAGTCAATGA | 55213 |
rs566892292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546371 | TGGGTGGAAGGGAAA[A/G]AAGTTATCTAGGACA | 55213 |
rs566928969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564182 | ATCAACCTGCATCCC[C/T]GGTTCTTTCAATATG | 55213 |
rs566967008 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557777 | AAAAATTTTTTTTTT[A/T]AAAGAATGAATTCTA | 55213 |
rs566969708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584769 | GCTGCAGAGTTCCGC[A/C]GATGGCTTGAAAGTG | 55213 |
rs567029507 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569776 | GCCAGGCATGGTGGC[A/G]CATGCCTGCAGTCTC | 55213 |
rs567033769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584171 | ATTTTTTAAAAGCTA[A/C]AAGCTTGACAGCTTT | 55213 |
rs567112014 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532433 | TTCACATTTTGCTCA[A/G]ATCATAAGCCTATAG | 55213 |
rs567126304 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575804 | TATGCTCACTACCTG[C/G]GTGACGGAATTATTC | 55213 |
rs567257910 | in-del | -/CA | 0.0154538 | 0.0865337 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534514 | ACACACACGCGCGCG[-/CA]CACACACACACACAC | 55213 |
rs567347016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544409 | GGGAGGCAGAGGTTG[C/T]GGTGAGCTGAGATCG | 55213 |
rs567383828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545163 | GGTACTTCATGATAA[C/T]ATAATAACCCCCTCT | 55213 |
rs567457227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564305 | TTAGAAAAATGTACC[A/G]GCCGGGCACAGTGGC | 55213 |
rs567597026 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539105 | AAACTCCTGATCTCA[A/T]GTGGCCCACCTTGGC | 55213 |
rs567598851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546802 | GATGGGGAGCAGCTG[C/T]AAATACAGATGAAGC | 55213 |
rs567599658 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580456 | AGTCATAATGGTGTG[C/T]GCCTGTAGTTAGTCC | 55213 |
rs567611689 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538346 | ACTCACTGTATCTTG[C/T]AGCATTCAGGAAATA | 55213 |
rs567687830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584296 | TGAATATGCTTCCTC[G/T]TCAAGAGAAACAGAC | 55213 |
rs567716601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558484 | ATCACCTGAGGTCAG[A/G]AGTTCGAGACCAGCC | 55213 |
rs567777558 | snp | C/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579262 | GCTGAGACACTAATA[C/T]GTTATTGCCCCAGCT | 55213 |
rs567824120 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578598 | AGGAAATGAATGTAT[C/G]ATGCAAGTATATGGT | 55213 |
rs567862913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571707 | TTAACTTGGGCGCGT[A/G]GCATTTCCCTCCTAA | 55213 |
rs567997783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584835 | TATGCGAGCAGAACA[C/G]AGCGTGCTCGATAGT | 55213 |
rs567999268 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583776 | TGGTCTTGAACTCCT[A/G]GCCTCGTGTAATCTG | 55213 |
rs568030688 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560505 | GGCGTGTGGCTACTC[G/T]CTCACCAAGTATAGG | 55213 |
rs568063029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554980 | GCATCCAGAGACTAA[G/T]TTCACAGAAATAACC | 55213 |
rs568071796 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586866 | TTTACCACTTCAACT[A/C]CTGTTTGGCTCTGGT | 55213 |
rs568102286 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568657 | TCAGGCCGGGGGAGG[C/G]GGGTGGCTCACACCT | 55213 |
rs568113769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536847 | GTCATTAGCAAAGAA[A/G]ACAAAAATAAAAACT | 55213 |
rs568140679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562347 | ATCATGAAGATCAGG[C/T]CAGGCATGGTGGCTC | 55213 |
rs568247941 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574470 | TAAAATGAACAAATA[-/T]TTCCAATGAAAATAA | 55213 |
rs568260685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582071 | TTTTTAATGTAAACA[C/T]TGTTAGAGGCTTGAA | 55213 |
rs568307594 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571700 | AGGGTCCTTAACTTG[C/G]GCGCGTGGCATTTCC | 55213 |
rs568492808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574737 | TAAACTCCATTTCTA[C/G]CATATACCCCAAAGA | 55213 |
rs568529827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537399 | TTTGTCAGCCTACTG[C/T]TGATCAAAGACTTTT | 55213 |
rs568600413 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546901 | TATGGCCTGGGGTGT[A/G]GGGACCCCTGATCTA | 55213 |
rs568614163 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566307 | AAATAAATAAATAAA[A/T]AAGTTGCATTGCAAC | 55213 |
rs568764340 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534687 | AGATGTGGGTTAGTT[C/T]AAGAAACAGAAAGGT | 55213 |
rs568770766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550790 | ACCTCATGTTCATTC[C/T]GGCTACTACTCAAAA | 55213 |
rs568826563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555944 | GCTTGAGGTACCAAA[A/G]CTGGTAAGTAGCGCT | 55213 |
rs568846301 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564107 | GATTACACACACATA[C/G]AAAATGTCCACTCTC | 55213 |
rs568881114 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557224 | AGGACAGCAAAGCAA[A/G]ACTGGACAGACGGAT | 55213 |
rs568916747 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531618 | ACCTCTTCCTAACAC[A/G]CCAGGGATGAATATG | 55213 |
rs568995195 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568716 | TGGGCAGATCAGGAG[A/G]TCAAGAGATCGAGAC | 55213 |
rs569006511 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532141 | TAAGAGTTGTCATAT[C/T]CTGCTATGATTAACA | 55213 |
rs569070618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575598 | GAACAAAATCATGGA[C/T]GCAGCTACAGGCCAT | 55213 |
rs569115236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543568 | TTTACCTAAATTTCC[A/T]AAAAGACTTGTAAAT | 55213 |
rs569133521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582213 | ACAGAAGCGCCGGGC[A/G]CAGTGGCTCATGCCT | 55213 |
rs569182645 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548143 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 55213 |
rs569191625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557751 | ATAGCCAGATTCTTG[C/T]CTCTACAAAAAAAAA | 55213 |
rs569211113 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545289 | TCAGCATACCCAACT[C/G]AAGGAGGTGCAAGAA | 55213 |
rs569240815 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573507 | AAGCTGGAGTGCTGT[A/G]GCACGATCTTGGCTC | 55213 |
rs569299353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566213 | ACTATTGTCCTATGA[C/T]CCTGCCAAATCCCCC | 55213 |
rs569363980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565431 | CAGCCTCTGCCCGGC[C/T]GCCACCCCGTCTGGG | 55213 |
rs569390099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545243 | AAACACTAAGAATAT[A/C]TTTTTTCTGCTTTGG | 55213 |
rs569433961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551227 | AATGAGAATGTTAAT[A/G]AACAGAAGAATCACA | 55213 |
rs569468753 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544452 | CCAGCCTGAGCAACA[A/G]GAGTGAAACTCTGTC | 55213 |
rs569521933 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550672 | CCTTACTTGTCTTCC[A/C]TACTAAAAGGGCAAC | 55213 |
rs569558635 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565760 | CCACCCCGTCTGGGA[A/G]GTGTACCCAACAGCT | 55213 |
rs569648920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534756 | AAGAAAATCCCAGCC[A/G]GGCACGGTGGCTCAC | 55213 |
rs569791110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548623 | GGAATATTATTCAGT[C/G]ATAAAAGGGAATGAA | 55213 |
rs569857811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554457 | GATTTTTTAAAAAAT[A/G]AGTTAACATAAGGTC | 55213 |
rs569938405 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548056 | AGTGCTGAGATTACA[A/G]GTGTGAGCCACCACA | 55213 |
rs569975843 | in-del | -/A | 0.442431 | 0.159594 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564894 | AGACTCCGTCTCAAA[-/A]AAAAAAAGAAAGAAA | 55213 |
rs570031867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573027 | TCCTTCCCATGGTGC[A/T]ATGGTTTGTCCAAAT | 55213 |
rs570161459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554531 | CCCAGCTCATGAGCC[A/G]CAGGCCGGTACCAGT | 55213 |
rs570161715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560342 | CAAAAGCAAAGTTTA[C/T]GTATGCAAGAATTAG | 55213 |
rs570178529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542130 | GAGGCAGGAGAATCG[C/G]TTGAACCCGGGAGGT | 55213 |
rs570289864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561366 | GACATGTGGCTCACA[A/G]GAGCCATTCCCTCCT | 55213 |
rs570338214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567415 | ACTAACAAAAGCTGA[C/T]TCTAGAATAAATGAA | 55213 |
rs570356636 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564283 | GAAAGCCAGGTAGCA[C/T]CTATGTTTAGAAAAA | 55213 |
rs570372783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560636 | TTTTTTTACATAAAG[C/T]AACCATTTTTTTACG | 55213 |
rs570394238 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554832 | CAGTCCCTGGTGCCA[A/T]AAAGGTTGGGGACCA | 55213 |
rs570398463 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551125 | GGGAAGGGAAGGGAA[-/G]GGGGGAGGGAGAAGG | 55213 |
rs570422871 | snp | A/T | 1.65529e-05 | 0.00287683 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566760 | ATAGTTCAGTCCAAA[A/T]ACAAAGACCTAGAAA | 55213 |
rs570506957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574169 | TGTTGCCCAGTCTGG[A/T]GTACACTGGCACCAT | 55213 |
rs570570135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573609 | GCCCACCATCACGCC[C/T]GGCTAATTTTGCATT | 55213 |
rs570628159 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574119 | TAGTCCCAAATTTCT[G/T]TTTTTGGGGGTGGGG | 55213 |
rs570675097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549357 | AAAGCTAATAGAGAA[C/T]AAAACATTCTGAGAG | 55213 |
rs570793517 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568266 | TGGCATTCCATTACA[A/T]CGATTTAGCAATTTA | 55213 |
rs570847553 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554204 | TATACTCACCCATAT[A/G]TAATTGTTTAAGGGA | 55213 |
rs570900388 | in-del | -/GACGCTACCCAGCC | 0.00398564 | 0.0444627 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585630 | GCAGCGCGCGCCCGG[-/GACGCTACCCAGCC]GAGCATCCCGCACCG | 55213 |
rs570921610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542720 | CCTTTTTTTTTTTTG[C/T]ATTGCCTGTTCCCCT | 55213 |
rs570950577 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552922 | GGTGGGGTAGCTCAC[A/G]CCTGTAATCCCAGCA | 55213 |
rs570954882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536105 | ACTTTATACACTCAT[G/T]AAAATGGTTCTATCA | 55213 |
rs570991708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536712 | GAAGTGGAGAGTATA[A/G]AAACAGAAGGGTCTA | 55213 |
rs571009861 | in-del | -/TGAC | 0.41833 | 0.184838 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535011 | GCACTCTAGCCTGGG[-/TGAC]TGACAGAGCAGAGGC | 55213 |
rs571027721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561560 | CTGAAAACAGAAAAA[C/T]AGACTTAAATAGAGA | 55213 |
rs571105525 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567267 | AGATGGGCCACTTTC[C/T]GACATCCACCATGAC | 55213 |
rs571106683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556546 | AATTAGGGAGGGAGG[G/T]GTTGGCAGTAGAGGA | 55213 |
rs571172173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556093 | ATCAATAGGAAATGC[A/G]GTATATGCCACATAA | 55213 |
rs571176190 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536685 | AAGTCCTCTTATAGC[C/T]CATGGAATAGGGAAG | 55213 |
rs571285661 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542979 | AGAAAAAGTATTCTG[A/C]GGTGCAGTGGCTCAA | 55213 |
rs571383292 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539080 | TCACCATGTTGGCCA[G/T]GCTGGTCTCAAACTC | 55213 |
rs571462424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565313 | GAGTCTCGTTCACTC[A/G]GTGCTCAATGTTGCC | 55213 |
rs571507552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547803 | GTTGTTTGCTTTTTT[A/T]ATTGAGACAGGGTCT | 55213 |
rs571512413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559351 | AGAGTAATCAAACTC[A/G]AAGAAACAGAGTAGA | 55213 |
rs571572774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558566 | AGGCATGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 55213 |
rs571575895 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539777 | ATTCCATCTGTTGTC[C/G]GGCTGCAGACAAAGT | 55213 |
rs571632706 | snp | A/G | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531764 | AATGACCATTCTACT[A/G]TGTCTCAATGAATTT | 55213 |
rs571636970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534803 | CTTTGGGAGGCCGAG[A/G]CGGGCGGATCACTTG | 55213 |
rs571651443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584919 | ACTTATTTAGAGTTC[A/C]CCGCACGCCTGGATA | 55213 |
rs571688483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585241 | GAGAGCACATTAGCT[A/G]AGGTGCTGGCGGGGC | 55213 |
rs571734059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546861 | TGCAACCCAGTTAAT[A/G]ACAGGCCACGGACCA | 55213 |
rs571750693 | in-del | -/T | 0.47071 | 0.117418 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560613 | GAAATCTGGCTGAAT[-/T]TTTTTTTTTTTTTTA | 55213 |
rs571781393 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572862 | AGATGCTTCAAATAG[C/G]AAGATATGAAGTGAT | 55213 |
rs571790127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553718 | GGTAACATGATGGAG[C/T]GGAAAGGGGGAATGG | 55213 |
rs571805572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572276 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 55213 |
rs571865912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579882 | GAGGAAAATGTAAGT[A/T]CCTACAACTGTCATT | 55213 |
rs571899015 | snp | A/C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556599 | AAATGTCTAAGCCCC[A/C/T]GCTCCCCACCCTGCT | 55213 |
rs571928569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579321 | TTCTGCAAACACACA[A/G]TACTACAAGAATGAA | 55213 |
rs571940034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565004 | CAGCTGTCCCGCTCC[C/T]GCTCCCATTCCCACT | 55213 |
rs571996774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558124 | TCTGCATGTCCCATG[C/T]CTGTGTGGGTTTTCT | 55213 |
rs572083159 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580078 | GCAATAGCATTAGCA[A/G]TGAAAAAAATAACAT | 55213 |
rs572170260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584454 | TTACATCCTCGACCC[C/T]GAAAGCAGTTTAAAC | 55213 |
rs572232765 | in-del | -/GAA | 0.316243 | 0.241064 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566054 | GTTAAACAGATGCTT[-/GAA]GAAGGCAGCATGCTC | 55213 |
rs572242778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539133 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 55213 |
rs572309082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546980 | TGTTAGGACATTTGT[C/T]CTGAAAAGAATGCCT | 55213 |
rs572370981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546519 | ACTTAATTTTTATTA[C/T]TGTTACACTGTAATA | 55213 |
rs572425021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539870 | ACATTTTGAAAACAT[C/T]GTGGTCAACTTTGAT | 55213 |
rs572432594 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544536 | AAATACTTAAATTCC[C/T]ACATTACACTTTTTC | 55213 |
rs572474226 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547604 | TCAGCCAATAATGGA[C/G]TCTTAAAGAAGACAA | 55213 |
rs572485925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565749 | CTGCCCGGCCGCCAC[C/T]CCGTCTGGGAGGTGT | 55213 |
rs572487773 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533979 | CCTTGTTATGTTCCT[A/G]CACAAACAACTGTGT | 55213 |
rs572490119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572350 | AAAAAAAAATGCAGG[A/T]TCCATTGCAAGGAAC | 55213 |
rs572496106 | snp | A/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582129 | GTAGAAACATCAAAG[A/T]GGAGAGGATGTAACA | 55213 |
rs572513822 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548844 | AAGGGCTTTCTTCTG[A/G]GGTGATTAAAACAAT | 55213 |
rs572578815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554156 | AAAAGCTGCAGTAGG[G/T]ATAATCATCCCATTT | 55213 |
rs572604385 | snp | G/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546841 | CTGCCACTCACCTCC[G/T]GCCGTGCAACCCAGT | 55213 |
rs572862846 | snp | C/G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573092 | GCTGCCACCCAAACA[C/G/T]GTCATACAGCTAAAC | 55213 |
rs572866348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557043 | TGGGGCATGAGGCCT[A/G]TGTGCTATGCCTGGC | 55213 |
rs572895131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574926 | GAGGAAATTCTGATA[C/T]ATACAACAACAGGGA | 55213 |
rs572917466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537018 | TGGTCTTAATATCCT[C/T]ATTTTAAAAAATGCT | 55213 |
rs572953539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581702 | CTGTGAAGGAAGAGG[C/T]AGACCAGGAGGAAAA | 55213 |
rs572967309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557429 | GAGTGACCTTTAAGA[C/T]AAGCACAACTTGGGG | 55213 |
rs572984854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562821 | TAAGAGACATGGCCT[C/T]GCTATGTTGACCAGG | 55213 |
rs573080967 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569641 | GAATCACTTGAGCCC[G/T]GGAGGCAGAGGTGGC | 55213 |
rs573119254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570116 | AAATGTTTAATTTTA[C/T]ATGACACAGAATTAG | 55213 |
rs573238182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544571 | ACGCTCCATGAGTGT[A/T]CACAAAAAACTCTTT | 55213 |
rs573243233 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575867 | CATGTAACAAACCTG[C/T]ATATGTACTCCCTGA | 55213 |
rs573247410 | in-del | -/G | 0.0244538 | 0.107838 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579624 | TCGAGACTTGTCTCA[-/G]AAAAAAAAAAAAAAA | 55213 |
rs573307461 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543353 | TAAAAAAGAAATAGT[C/T]GTCTAAGAAAGAATC | 55213 |
rs573425883 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533318 | ACAATTTAAACTTGA[C/G]TTCTCAAGTTCTACC | 55213 |
rs573499785 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583585 | GGAGTCTCACTGTGT[C/T]GCCCAGGCTGGAGTG | 55213 |
rs573592323 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532633 | TATCTATTTCAGCTA[C/T]CAGTGAATTCCTATC | 55213 |
rs573658009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537581 | GCTTAGCACACAGGA[C/T]TTCTGGAAAGTTCTC | 55213 |
rs573694841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562959 | GAAATATTACAAGAA[A/G]AAATTTCCAGAAATG | 55213 |
rs573765605 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544675 | TTATCAGTACTCATT[C/T]TGTGGAATAACAAAG | 55213 |
rs573773665 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532403 | CAAGTAAGAGCAATA[A/G]TAAACATACTGAAGT | 55213 |
rs573799741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545600 | ACTTGTACAAATTCC[C/T]GGAATGCTTTCTTGT | 55213 |
rs573807397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556951 | ACATCACATTCCCTT[A/G]CAGTGCTGCTGACTC | 55213 |
rs573955319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570213 | TTCCTGACAGCAGCA[C/T]AATTATTCTAAAATC | 55213 |
rs573979169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553375 | GTCATTTCTTCCCTC[A/G]TTAGCAAATAGGTGA | 55213 |
rs574003317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576598 | GCAATTTAAACCAGA[C/T]CAAACAAATTGCTAA | 55213 |
rs574018878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551984 | TTTTTTTAACTTGTC[A/G]AGCCTGTTTTGCCAA | 55213 |
rs574044850 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560158 | TCTTCCCCAGAACTT[C/T]GTACAGCTCCTTCTC | 55213 |
rs574098834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583101 | ACTTGAGCCTGGGAG[C/T]TTGAGGCTGCAGTGA | 55213 |
rs574150690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571068 | AAAAAGTATCCAGGC[C/T]GGGCGGGGTAGCTCA | 55213 |
rs574197025 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541118 | GAAGTTTCTTAGTGG[A/G/T]TAAGATTCTGAATTT | 55213 |
rs574259534 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533426 | ATTATCAACTTTTCA[C/T]GGATACTTCTAAATT | 55213 |
rs574273099 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533817 | CCAAGTTCAGAAGTT[C/T]CTCTAATCAAAAATG | 55213 |
rs574277682 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553214 | CAGAGGGAAAGTGAC[-/A]AAAAAACCTACCAGG | 55213 |
rs574305551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567760 | CCCACCAGCACCAAC[C/T]TGGATGACAAGGATC | 55213 |
rs574314146 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586126 | AGGTGGCAGCTGGAC[A/C]AAGGTATGAAGGAAG | 55213 |
rs574339009 | in-del | -/TA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548604 | TGGTGTATATATATA[-/TA]ATGGAATATTATTCA | 55213 |
rs574351630 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49580546 | TGAGCCGTGTTCACA[C/T]CACTGTATTCCAGTC | 55213 |
rs574524538 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585545 | GGTGCCCACCGGCAG[A/C]GAAGAGGAGGAGCGC | 55213 |
rs574623742 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557862 | TGCACTCCCACAAGG[-/T]TTTTTAGCTACATGC | 55213 |
rs574690415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536279 | AACCTTGGTTGAGGC[A/G]GATCTATGTAAAAGG | 55213 |
rs574759203 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587056 | CCAGAATACTATATA[C/T]ATTCTGATACACCTC | 55213 |
rs574807861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556259 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG | 55213 |
rs574832850 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543718 | TTTTTTTTTCATTTT[C/T]GAGATAAGATCTCAC | 55213 |
rs574840671 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551960 | ACTGAATTTTTCCAT[-/T]TTTTTTTTTTTTTTT | 55213 |
rs574849999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536342 | AATTTGCAAGTTCAC[C/T]AGAGAGTCGCACAGT | 55213 |
rs574957659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574415 | TGAGCCACCATGCTC[A/G]GCCAGTCCCAAATTT | 55213 |
rs574973693 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586107 | GCAGGCCAGGGACTA[A/G]GGAAGGTGGCAGCTG | 55213 |
rs574977658 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541888 | AAAAAAGAAAAAAAA[A/T]TTACCTAATTAAGTT | 55213 |
rs574978453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582332 | TCTCTATTAAAAATA[C/T]AAAAATTAGCTGGGC | 55213 |
rs575013504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535840 | CCAGCTTGACCAACA[C/T]GGTGAAACCCCGTCT | 55213 |
rs575015481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542392 | AATAGGTATACATAG[A/G]GCCTGGAAGTACCTA | 55213 |
rs575125365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543786 | GATCTACTGGGCTCA[A/G]GCAATCCTTCCACCT | 55213 |
rs575133023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561815 | CCTATAACAAGTTTC[C/T]ATGAGGCTGGGCTTG | 55213 |
rs575142805 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558020 | GCTTACAGCAGGTCC[C/T]TGAAAAACGTCATTT | 55213 |
rs575152365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573739 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCTTCTT | 55213 |
rs575153906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550140 | TGCACCACCATACCC[G/T]GCTAAGTTTTGTATT | 55213 |
rs575215219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543063 | AGGTCAGGAGTTTGA[A/G]ACCGGCCTGGCCAAC | 55213 |
rs575243529 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535199 | GTTTTCAGTCAAACA[G/T]AAGTCACCAACTACC | 55213 |
rs575303721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556319 | CTCCTACCTCCCAAG[C/T]AGCTGGGACGACAGG | 55213 |
rs575407181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567772 | AACTTGGATGACAAG[A/G]ATCAGCTTCAGCCCC | 55213 |
rs575416694 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582994 | CCAGCCTGGGCAACA[C/T]AGGGAGACCCTGTCT | 55213 |
rs575456780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574266 | TGAGATTACAGGTGT[A/G]CACCACCACGCCTGG | 55213 |
rs575490709 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534805 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACTTGAG | 55213 |
rs575638394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550816 | CAAAACACTTTTGCA[C/T]AGGCCAGGCACGGTG | 55213 |
rs575763632 | in-del | -/GT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583412 | TGTGTGTGTGTGTGT[-/GT]TTTAAATGTGATCTA | 55213 |
rs575813066 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587358 | GTCTGAGAGAAAAAC[A/G]AGGGCATGGGGTGTG | 55213 |
rs575821496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585441 | CCCGCGCCCACACGC[C/T]ACCTGCGAGGTCAGC | 55213 |
rs575862609 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531858 | GCATAATATCCTCAA[C/G]TTCACCTCTGTGCAC | 55213 |
rs575981955 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553395 | CAAATAGGTGAGCTC[C/T]GATGAGGCTCTAAAC | 55213 |
rs576027845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537729 | ACAATGTTTTATCCA[C/T]ATTTTCTCCCTGATG | 55213 |
rs576152274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546619 | ACTGGACGGCCCCAT[A/C]TGGGGGTGATGGGAG | 55213 |
rs576171861 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578933 | ATAAGAGAGCTCTAC[A/G]GTTTGGGGTAAACTT | 55213 |
rs576179649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579497 | GGCCTGGTAGTGGGC[A/G]CCTGTAGTCCCAGCT | 55213 |
rs576347337 | in-del | -/TCT | 0.00795532 | 0.062565 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560985 | CAACCCGGAAGCTCC[-/TCT]GTCTGAATTTTTTTT | 55213 |
rs576348754 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534522 | CGCGCGCGCACACAC[A/T]CACACACGCAAGATC | 55213 |
rs576355720 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546588 | TCAGTGGGAGTCCTG[A/G]GCTTGTTTTCCTACA | 55213 |
rs576409722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540141 | TCAGCTCACTGATCA[A/T]CCTTAATGCTTCCTT | 55213 |
rs576503086 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559524 | AGGCGGGTGTGGTGG[C/T]GGGTGCCTGTAGTCC | 55213 |
rs576503992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559572 | GAGGCAGGAAAATGG[C/T]GTAAACCCGGGAGGC | 55213 |
rs576507296 | in-del | -/A | 0.0109229 | 0.0730898 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559879 | GTATTTACTATGATG[-/A]AAAAAAAAAAGAATA | 55213 |
rs576523922 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581752 | AGAGATCTGGGGACT[C/G/T]GAGCATCACAGGCAA | 55213 |
rs576539615 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559623 | ATCGTGCCACTGTAC[C/T]CCAGCCTGGGCGACA | 55213 |
rs576593923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534974 | GGGAGGCAGAGGTTG[C/T]GGTGAGCCGAGATCG | 55213 |
rs576605372 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549002 | GCTGGGTGTGGTGGC[G/T]GGTGCCTGTAGTCTT | 55213 |
rs576661663 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548205 | GACCAGCCTGATCAA[C/T]ATTGTGAAACTCTGT | 55213 |
rs576727144 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586276 | AGTAAACTGAGGCCA[A/G]GAGAGGGACTGCTAC | 55213 |
rs576748430 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568833 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 55213 |
rs576782245 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585498 | CAGGGATCTCCGAAG[C/T]TCCAATGGGCGCAGA | 55213 |
rs576811245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548118 | ATTTTTGGACCAGGC[A/G]CAGTGGCTCACGCCT | 55213 |
rs577049537 | snp | C/T | 1.65053e-05 | 0.0028727 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540955 | TTGATAATGTGCTGA[C/T]AAAGTTTTTTCAGTC | 55213 |
rs577065274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535749 | TAAACCACAGGCCAG[A/G]CGTGGTGGCTCACGC | 55213 |
rs577099505 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586079 | CCTCACTTCCTGATT[G/T]AAAGTACCTGAGGCA | 55213 |
rs577127099 | snp | C/G | | | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551446 | TCTGTTAGTGCTAGA[C/G]TATGTGCGTAACCGC | 55213 |
rs577166126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560157 | TTCTTCCCCAGAACT[G/T]CGTACAGCTCCTTCT | 55213 |
rs577174062 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566586 | CGGTCAATTTCTTAC[A/C]AACTGAAAAGTTAGA | 55213 |
rs577225821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535003 | CGCACCACTGCACTC[C/T]AGCCTGGGTGACAGA | 55213 |
rs577226561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567019 | AAAAAAGAGAAACTA[C/T]CAAAGCCATAGTCTT | 55213 |
rs577383111 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578625 | TGGTCCATGTGACAC[-/AT]GTTAATATGTCAAAT | 55213 |
rs577389068 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587452 | GGAGGATTAAAAGCT[G/T]AATGAGACATGGTTG | 55213 |
rs577440005 | snp | A/G | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531598 | CACTCACCTCCCGCT[A/G]TGCGACCTCTTCCTA | 55213 |
rs577518343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581465 | GGTGATGAGTCCTAC[C/T]ATGGACATTTGTGCC | 55213 |
rs577561033 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550102 | TCAAGCAATCCTTCC[A/C]CCTCAGCTTCCCAGA | 55213 |
rs577598127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564504 | GGCAGAAGAATCGCT[C/T]GAACCCAGGAGATGG | 55213 |
rs577624903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569584 | GCCTGGCGGTAGTGG[C/T]GCATGCCTGTAATCC | 55213 |
rs577700599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539026 | AGGTACGCACCACCA[C/T]ACCCAGCTAATTTTT | 55213 |
rs577852547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559432 | GAGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG | 55213 |
rs577869294 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557433 | GACCTTTAAGATAAG[C/T]ACAACTTGGGGGCTT | 55213 |
rs577908435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534489 | TCTAACTCAAAGTAC[A/G]ACTCTTCAAAACACA | 55213 |
rs577986509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571117 | TTTGAGAGGCCGAGG[C/T]GGGCGGACCACCTGA | 55213 |
rs578022001 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546482 | GTTTGGGGATGATTC[A/G]AGCACATTATGTTTA | 55213 |
rs578058221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577802 | AAACATTCTTCAGCA[C/T]ACAAGCTACAGCAAG | 55213 |
rs578106965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565595 | GCCCGGCCGCCCATC[A/G]TCTGGGATGTGAGGA | 55213 |
rs578152924 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571734 | CTAAGGCAGCAGAGC[C/G]TAACTGTAAATACCA | 55213 |
rs578165849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565150 | CTGCCGAGTGCCTGC[C/G]ATTGCAGGGGCGCGC | 55213 |
rs578176274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584360 | ATTAATAAATAGACT[A/G]ATATTCACACAATGG | 55213 |
rs745312513 | snp | A/G | 3.40397e-05 | 0.00412537 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555650 | TCCCACTTGGCCACA[A/G]TTGTTATAACCCCAA | 55213 |
rs745321467 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581548 | TCTGAAGCTCAAGAA[A/G]GGTCTGGATTGGAGA | 55213 |
rs745337208 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560027 | GCAATGCCTTGGTTG[G/T]TCGTCCCATTCCCAA | 55213 |
rs745394427 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583366 | CTTTTCTACCCCAGG[A/T]AAGAAGTGTGCTTTT | 55213 |
rs745418094 | snp | C/T | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544764 | ACAGCTTTATGGACA[C/T]GAATATATTTTCCAT | 55213 |
rs745573114 | snp | A/G | 3.31846e-05 | 0.00407323 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544881 | GAAGGCAACAAACAT[A/G]TATTAATATGGCAAG | 55213 |
rs745612793 | snp | C/T | 1.67393e-05 | 0.00289299 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549633 | GGCAGAGTGACAGGC[C/T]GCAATCTCTACCACC | 55213 |
rs745619192 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550710 | CTGCAGTAATTATAC[C/T]AAGATGCATTCACAC | 55213 |
rs745685467 | snp | A/G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556246 | CTGTCCCCCAGGCTG[A/G/T]AGTGCAGTGGTGCGA | 55213 |
rs745694838 | snp | G/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534178 | ATTCCTTTAGCAGAG[G/T]GCCATCCATTTGCCA | 55213 |
rs745771042 | in-del | -/T | 1.77351e-05 | 0.00297779 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555676 | CCAAGCAAACACCTA[-/T]CAAGAGAAAGAAAAA | 55213 |
rs745851612 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533720 | CTCTCCATTCATCTC[A/T]CAATTCCCCAACTAT | 55213 |
rs745871171 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587510 | TTATTCCAGTACAGG[A/G]TGAAAAGTATTATGA | 55213 |
rs745882696 | snp | A/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555523 | ACCTCACCTCGCCAT[A/T]GTCCAGAACAGCCAT | 55213 |
rs745890694 | snp | A/G | 3.29984e-05 | 0.00406179 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540950 | CTCTCTTGATAATGT[A/G]CTGACAAAGTTTTTT | 55213 |
rs745938057 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576982 | TTCGTATTTTCTCTG[G/T]CACTTGAAAATACAT | 55213 |
rs746032312 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554010 | CAGTAGAGCTCTGTA[C/T]GTGGGTCATTCACAG | 55213 |
rs746102926 | in-del | -/CCTA | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586045 | TTTACTGGAGACGCG[-/CCTA]CCTCCCTCCCTCCCC | 55213 |
rs746108134 | in-del | -/C | 1.65124e-05 | 0.00287331 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534118 | AACCCAGCAGCCTTG[-/C]GCTTCAGTTCTTAAA | 55213 |
rs746160838 | snp | A/C | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586718 | CCACCTCCCCCACTT[A/C]AAGAAAACCAGGGCC | 55213 |
rs746165017 | in-del | -/AGAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535565 | CGAGGTGGGAATGTT[-/AGAC]AGACAGAGTGGAAGG | 55213 |
rs746184983 | snp | C/T | 1.70504e-05 | 0.00291975 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566786 | AGAAAATAGATAGTT[C/T]TTTTTCTGAGTCTTT | 55213 |
rs746212488 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541557 | ATACTTACTTCAAAT[C/G]TTTTTTAAGCACCAA | 55213 |
rs746214772 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541957 | GTGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 55213 |
rs746218573 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545133 | AAATGTATATTTTTA[A/G]AGAAAAAAATTATAG | 55213 |
rs746234843 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571441 | CATGAATGTCATTTA[C/T]TCCTGCACTTTTGCA | 55213 |
rs746261015 | in-del | -/GT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583384 | GAAGTGTGCTTTTGT[-/GT]ATGTGTGTGTGTGTG | 55213 |
rs746325362 | snp | A/C/T | 4.94281e-05 | 0.00497112 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551433 | CAGCAAGCCCTCATC[A/C/T]GTTAGTGCTAGAGTA | 55213 |
rs746344293 | snp | C/T | 1.68386e-05 | 0.00290155 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567132 | AGTCCTAAAACGAAA[C/T]TAGGTTTCAAGAGAC | 55213 |
rs746376392 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533370 | GGATAAGTAGTGGAG[A/T]TTCTAATTTATAAAA | 55213 |
rs746417154 | snp | A/G | 1.6666e-05 | 0.00288664 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540837 | ACGAGCACAAAGGGA[A/G]TTAAAGGTGGTCTGG | 55213 |
rs746430833 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572698 | AATCTCAGCTACTCA[A/G]GAGGCTGAGGTGGGA | 55213 |
rs746432143 | snp | A/G | 9.06988e-05 | 0.00673359 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552134 | CCAAGTTAGAGCAAG[A/G]AAGGTAGATGGGAAG | 55213 |
rs746471811 | snp | A/G | 6.83013e-05 | 0.00584346 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552293 | CCATATACCTTAGAG[A/G]GGACAGAAGGGAGAG | 55213 |
rs746505394 | in-del | -/CAATA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541054 | ATGTATAATAATTTC[-/CAATA]CACAGAGATTTTGTT | 55213 |
rs746546621 | in-del | -/TATACTA | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533242 | TTAGGAAGGCAAGAG[-/TATACTA]TACATGTCATTATTT | 55213 |
rs746564535 | in-del | -/T | 5.10083e-05 | 0.0050499 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566784 | CTAGAAAATAGATAG[-/T]TTTTTTTCTGAGTCT | 55213 |
rs746630630 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539873 | TTTTGAAAACATCGT[A/G]GTCAACTTTGATCCC | 55213 |
rs746731185 | snp | G/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541777 | ATTTCTATCACTTCC[G/T]TCATGTCTTCATTCC | 55213 |
rs746732852 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569648 | TTGAGCCCGGGAGGC[A/G]GAGGTGGCTGTGAGC | 55213 |
rs746748115 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570607 | TTTTATGTTCAAGAT[A/G]TAATGAAGAAGCTGG | 55213 |
rs746753718 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563638 | CACTCCAGCCTAGGC[C/G]ATAGAGCGAGACTGT | 55213 |
rs746805563 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558039 | AAAACGTCATTTCAT[G/T]CAACATCATTTTGTT | 55213 |
rs746826785 | snp | C/T | 1.64999e-05 | 0.00287222 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549551 | GGTGCGGGAGGATCA[C/T]GGACTGACCCCGGCA | 55213 |
rs746831849 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546814 | CTGTAAATACAGATG[A/C]AGCTTCGCTCACTGC | 55213 |
rs746886805 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548075 | TGAGCCACCACACCC[A/G]GCCGGTTCTTCACTT | 55213 |
rs747076959 | snp | C/G/T | 3.334e-05 | 0.00408276 | splice-acceptor-variant, utr-variant-5-prime | RCBTB1 | GRCh38.p7 | 13:49567322 | ATAAGCCGACATCTC[C/G/T]GCTGGAACAGAAAGG | 55213 |
rs747085794 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554371 | TTTAAAAATAAGAGA[A/T]GAATACTGGAATGGA | 55213 |
rs747121441 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540830 | GGGGGAGACGAGCAC[A/G]AAGGGAGTTAAAGGT | 55213 |
rs747130552 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555685 | ACACCTACAAGAGAA[A/C]GAAAAAGGAAAAGGA | 55213 |
rs747164058 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543419 | AATAGACTGGTTGAC[C/T]ACAGGTGCACAGACA | 55213 |
rs747207415 | in-del | -/AAAAA | 1.66424e-05 | 0.0028846 | frameshift-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544745 | AAATACCTGATTTTC[-/AAAAA]AAAACAGCTTTATGG | 55213 |
rs747267501 | snp | A/T | 1.66782e-05 | 0.0028877 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544738 | TCATGCAAAAATACC[A/T]GATTTTCAAAACAGC | 55213 |
rs747293132 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535480 | ACATTGAAGGTCAGC[A/T]CTCCGGGTTCTATCG | 55213 |
rs747348367 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572913 | GTATGAAGGAGGCAC[G/T]GCTAATGGAAAGAAC | 55213 |
rs747350280 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569739 | AAAAAAAGAAAGAAA[-/G]AAAGAAAAAGAAAAA | 55213 |
rs747362249 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544394 | GAATCACTTAAACCC[A/G]GGAGGCAGAGGTTGC | 55213 |
rs747403385 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560210 | TGCCCCCTCCTCTCT[A/G]TTAAGTAACCATGGA | 55213 |
rs747438938 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533575 | TTGAAGTTAAAAAAG[G/T]CATCAACGCAAGCAC | 55213 |
rs747449499 | snp | G/T | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566700 | GCCTTCTAGCTTTTT[G/T]GGTACAAGTGTACTC | 55213 |
rs747543214 | in-del | -/AAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575578 | TACTACATGGCCATA[-/AAG]AAGAACAAAATCATG | 55213 |
rs747566009 | snp | C/T | 1.66208e-05 | 0.00288273 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567154 | TCAAGAGACTCTTAC[C/T]TCATCATTGTCAGTA | 55213 |
rs747592294 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582496 | CTGTCTCTAAATAAA[C/T]AAATAAATAAATAAA | 55213 |
rs747615791 | snp | A/G | 3.37348e-05 | 0.00410685 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566780 | AGACCTAGAAAATAG[A/G]TAGTTTTTTTTCTGA | 55213 |
rs747635838 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569779 | AGGCATGGTGGCGCA[C/T]GCCTGCAGTCTCAGT | 55213 |
rs747696541 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570822 | TAATACTCTTGTGAG[C/G]AGGAGACTGTAAACC | 55213 |
rs747771304 | snp | C/G | 1.66255e-05 | 0.00288314 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567238 | CGCGATCTCTTGAGG[C/G]GAGAGTAGAGTGAAG | 55213 |
rs747803510 | in-del | -/TT | 1.66192e-05 | 0.00288259 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567232 | AATAGACGCGATCTC[-/TT]GAGGGGAGAGTAGAG | 55213 |
rs747895163 | snp | A/C | 1.64863e-05 | 0.00287104 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559938 | CATCAGCTGCCAGAG[A/C]CATTGAATGATGTGA | 55213 |
rs747895359 | snp | A/C | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552271 | ACCGTTGCCATTGTA[A/C]CCCCAGCCATATACC | 55213 |
rs747912403 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537136 | AGGGTGAGCAGGTGC[C/T]TCGGCATCACAGCTC | 55213 |
rs747916852 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586339 | CAGTCCCTTTGTAAA[A/G]TACCATACAGCTCTC | 55213 |
rs747995125 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536888 | AGTAATTTATAAATC[A/T]TTCCAAATCTTTCAA | 55213 |
rs748000256 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557994 | ACAGATGAATAGACA[A/G]ACAAAGTGTGGCTTA | 55213 |
rs748002852 | in-del | -/CTGCATCATATCTGACTGCAGCAGA/CTGCATCATATCTGACTGCAGCAGAGAATA/CTGCATCATATCTGACTGCAGCAGAGAATAGC/CTGCATCATATCTGACTGCAGCAGAGAATAGCGAAAA | 6.61986e-05 | 0.00575292 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49534264 | ATTCTTCTAAATCCT[lengthTooLong]GGACACACAACAAAA | 55213 |
rs748022757 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535715 | CAGAAACCCATCCAG[C/T]CACATAACCATTAAG | 55213 |
rs748125169 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537835 | GACAGTTTCATAACA[C/T]GTTCATAGCAAGGGA | 55213 |
rs748160587 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575252 | CAAAAAGTCAAAAAC[-/AA]AAGATATTGGCGAGG | 55213 |
rs748168580 | snp | C/G | 3.29473e-05 | 0.00405864 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566686 | TTCTTTCCACATAAG[C/G]CTTCTAGCTTTTTGG | 55213 |
rs748187912 | snp | C/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586179 | GGTATTGGAAAGAGG[C/G]AGAGGTACCTCGGAA | 55213 |
rs748244888 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587185 | TGGGTTTAGAACAGC[A/G]CCTGGCATGTGATAG | 55213 |
rs748253617 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555827 | CATTAACCTATTTAA[C/T]CTGCCTAGTAATCCT | 55213 |
rs748260501 | snp | A/C | 3.36763e-05 | 0.00410329 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549639 | GTGACAGGCTGCAAT[A/C]TCTACCACCCTGAAA | 55213 |
rs748308774 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544477 | TCTGTCTCAAAGAAA[C/G]AAACAAACAAACAAA | 55213 |
rs748367135 | snp | A/C | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534194 | GCCATCCATTTGCCA[A/C]AATGCTGCAGTCTGT | 55213 |
rs748379406 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574131 | TCTTTTTTTGGGGGT[A/G]GGGGGTGGACAGAGT | 55213 |
rs748419872 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551380 | TTATTTTTATTGCCA[A/G]TTCCCAGCTGCCCAT | 55213 |
rs748434517 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561169 | CATGGTAATAAAACA[A/T]CCTGACCTATTAAGG | 55213 |
rs748437879 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570606 | ATTTTATGTTCAAGA[C/T]ATAATGAAGAAGCTG | 55213 |
rs748450472 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578240 | TCTCCAGATTACTTA[C/T]AATACCTAATACAAT | 55213 |
rs748585258 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553053 | TGGGCGTGGTGGCGC[A/G]TGCCTGTAACCCCAG | 55213 |
rs748680186 | snp | A/G | 1.6638e-05 | 0.00288422 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544903 | TATGGCAAGTTCAAG[A/G]AACAGATTGAAGATT | 55213 |
rs748716776 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571389 | AATAAAAAGCATTCC[A/G]CAAAATGCTTCTGCC | 55213 |
rs748720503 | snp | A/G | 1.66765e-05 | 0.00288756 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566604 | CTGAAAAGTTAGATG[A/G]GTTCCCTCCTTACCT | 55213 |
rs748750585 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540103 | TATTCTCTCTGAATC[-/T]GTGAAACCAACCATA | 55213 |
rs748754334 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581644 | AAGAAGAACTCTAAG[A/G]AACTCCAACGGGAAA | 55213 |
rs748774773 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561340 | CACAAACTCAGAGTC[C/T]TCTTCCAGGTGACAT | 55213 |
rs748831620 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559325 | TATGATTCCACTTAC[A/G]TGAGGTACCTAGAGT | 55213 |
rs748860658 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546184 | TGCTTCAACTTCTGC[A/C]TCCAGTCTTAGGCTG | 55213 |
rs748883026 | snp | A/G | 0.000131781 | 0.00811621 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559989 | CTTGCTTGATCAAGA[A/G]ATTGGTACAGACCTG | 55213 |
rs749003892 | in-del | -/GAGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585060 | TAAGATCTTGGAAAG[-/GAGA]GAGAATAGGAAGAGT | 55213 |
rs749038455 | snp | A/G | 3.3325e-05 | 0.00408184 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567143 | GAAACTAGGTTTCAA[A/G]AGACTCTTACCTCAT | 55213 |
rs749063829 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578273 | AAATGCTTGGTAAAT[A/C]GTTGTTAACGTTTAT | 55213 |
rs749065884 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554216 | TATATAATTGTTTAA[A/G]GGAAAAGTCCAAAAA | 55213 |
rs749070509 | in-del | -/CAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535204 | CAGTCAAACAGAAGT[-/CAC]CAACTACCAACATTC | 55213 |
rs749073846 | in-del | -/TTATT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547951 | CACCACCACTCCTGG[-/TTATT]TTTTGTAGAGATGGG | 55213 |
rs749076368 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538056 | CACAGCACGAAGGCA[A/G]AGTCATCTAGCATCC | 55213 |
rs749080281 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550748 | TCACAGGTGGTTATT[G/T]CAGAGAGCTACATAA | 55213 |
rs749092803 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537048 | TAATGCCGCCTCTAA[C/G]GGAGTTCTTACCCTG | 55213 |
rs749104279 | in-del | -/CTCC/CTCCATC/CTCCATCAGCTGCCAGAGCCATTGAATGATGTGAGCC | 5.30626e-05 | 0.00515065 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49555675 | CCCAAGCAAACACCT[lengthTooLong]ACAAGAGAAAGAAAA | 55213 |
rs749105066 | snp | A/T | 3.38192e-05 | 0.00411199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534302 | CAAAAATGGCTTTTT[A/T]AGGCAACTTTGATTG | 55213 |
rs749115693 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567513 | ACCCCGGACTTTCCT[A/G]CAAGAGAATAACGTG | 55213 |
rs749118583 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554900 | GTGTCCAGGGTAATA[C/T]CTTTGTATAATTTTC | 55213 |
rs749223026 | snp | A/T | 1.79181e-05 | 0.00299311 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555679 | AAGCAAACACCTACA[A/T]GAGAAAGAAAAAGGA | 55213 |
rs749263936 | in-del | -/C | 1.66099e-05 | 0.00288178 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544893 | CATATATTAATATGG[-/C]AAGTTCAAGGAACAG | 55213 |
rs749302220 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583840 | ATGTAAGCCACTGCG[A/C]CTGGCCAATATGTAA | 55213 |
rs749308756 | snp | C/T | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544785 | TATTTTCCATCAATT[C/T]GAAACTTCAGATCAG | 55213 |
rs749411388 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539530 | AGCAAGGTCTGATCC[C/T]GAGTATGGAACTCGT | 55213 |
rs749435123 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535242 | AGTAACATCCACAAG[A/G]GGTAAACCAGAACCA | 55213 |
rs749483425 | snp | A/G | 1.68349e-05 | 0.00290123 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566573 | GCTTAGAATTAACCG[A/G]TCAATTTCTTACAAA | 55213 |
rs749557954 | snp | A/G | 1.65891e-05 | 0.00287998 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567224 | GCCTTCCGAATAGAC[A/G]CGATCTCTTGAGGGG | 55213 |
rs749564661 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569358 | CCGGAAGGACTGCTT[-/G]AGCCCAGCAGTTTGA | 55213 |
rs749581155 | snp | C/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567175 | ATTGTCAGTAACGTA[C/G]AGTGCTTCACTGGCT | 55213 |
rs749614249 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538490 | TGAGGTGGGAGGGAC[-/A]ACTTGAGCCCAGAAG | 55213 |
rs749672606 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582690 | TTTTACATGCCCACC[A/G]GCAATGTACAACAGT | 55213 |
rs749700049 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540275 | TTACAGTCTGATGCT[C/T]TGGTTCTTCAAAAAA | 55213 |
rs749704655 | snp | A/G | 2.69873e-05 | 0.00367327 | stop-gained, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552255 | TTCCCAGGCCCAGCT[A/G]ACCGTTGCCATTGTA | 55213 |
rs749709828 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553943 | GAGTAACATAGAAAA[A/T]CACCACAACTCTGTC | 55213 |
rs749822540 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583539 | TGCATTCTTCAGCAC[A/G]TACACAACATGTACT | 55213 |
rs749851821 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557140 | TCCTACTTAATAAAA[C/T]CTCTGTAACATCACT | 55213 |
rs749866741 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570927 | CTTATGGAGAATATC[A/C]GTCCTGGCCCTTGAA | 55213 |
rs749937846 | snp | A/T | 3.30551e-05 | 0.00406528 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540867 | GTTTCTGTTTGTTGT[A/T]TAAGTTACCTCTGCA | 55213 |
rs749954863 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574777 | AGAGACTTGAACAGA[C/T]AGTTGTATACCAACG | 55213 |
rs749983080 | snp | C/T | 3.30994e-05 | 0.004068 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559913 | AATAAAAGCAGCATA[C/T]TTACCTCTCCATCAG | 55213 |
rs750155872 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566751 | ACAGTTACTATAGTT[C/T]AGTCCAAATACAAAG | 55213 |
rs750173737 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552822 | GAAGGTATTGACTGT[A/G]TTAGAAGCTAGTTTA | 55213 |
rs750208458 | snp | C/T | 3.29761e-05 | 0.00406041 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551345 | CTTTCTCCACCATGA[C/T]GTGTGCTGGGCTTAG | 55213 |
rs750209268 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544158 | ATGGAAATGAGTATT[C/T]ACCAGATTCTTAATT | 55213 |
rs750277202 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553501 | ACAGTCCCTTGGATA[C/T]AGAGTGAGAGGAGGC | 55213 |
rs750340292 | snp | A/G | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540767 | GTTCACTGATTCCCT[A/G]AACAGAAGTGGAGTG | 55213 |
rs750411809 | in-del | -/ATAG | 0.00021733 | 0.010422 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566776 | ACAAAGACCTAGAAA[-/ATAG]ATAGTTTTTTTTCTG | 55213 |
rs750414418 | snp | A/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551455 | GCTAGAGTATGTGCG[A/T]AACCGCAGACAATCT | 55213 |
rs750461550 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559777 | TGTGGGTGCATGCTG[A/G]TGACAGTTGTATGAC | 55213 |
rs750464806 | snp | C/T | 3.31603e-05 | 0.00407174 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552243 | GGTTGCCATTGTTTC[C/T]CAGGCCCAGCTGACC | 55213 |
rs750496099 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577993 | TGCTAAGCTGTCTTA[C/T]GAAAAAAATTTATTT | 55213 |
rs750539238 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549860 | TTCTCATCCTCAGCT[C/G]ACTGTGAGTTAGGAT | 55213 |
rs750551924 | in-del | -/T | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531895 | TCAGAATTTCTTTCC[-/T]TTTTAAGGCTGCAGA | 55213 |
rs750557025 | snp | A/G | 0.000103956 | 0.00720881 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552337 | AACTGCTGGTAAGAA[A/G]GAAGAGACAAAAAAA | 55213 |
rs750597161 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579348 | TGAAAGGGAGGCCGG[A/G]CGTGGTGGCTCACAC | 55213 |
rs750645132 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538974 | TCCCAGATTCAAGCA[A/G]TTCTCCTGCCTCAGC | 55213 |
rs750700899 | snp | A/G | 8.25294e-05 | 0.00642323 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541713 | GTCGACTGTGTCTGT[A/G]TAGAGGTACTGGAGA | 55213 |
rs750706572 | in-del | -/AAAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543342 | TACCTGAGAAATAAA[-/AAAG]AAATAGTTGTCTAAG | 55213 |
rs750756518 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564300 | TATGTTTAGAAAAAT[C/G]TACCGGCCGGGCACA | 55213 |
rs750784974 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563158 | TAATCCCAACACTTT[A/G]GGAGGCCGAGCCACA | 55213 |
rs750786096 | snp | A/G/T | 3.37406e-05 | 0.00410723 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549473 | CCACAGACAGGAGGC[A/G/T]CCACGAGACGGCGGG | 55213 |
rs750790476 | in-del | -/TTCCT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547260 | GTTTCACTTTAAGGC[-/TTCCT]AAGCTTAACTCTTCC | 55213 |
rs750810375 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568102 | TGGAAACAGTGCTCA[C/T]GGAAGCACTACATGT | 55213 |
rs750863440 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569029 | TTATATTTATTCATT[A/C]ATTTAATCCTCACTT | 55213 |
rs750915195 | in-del | -/GC | 1.70321e-05 | 0.00291818 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549653 | CTCTACCACCCTGAA[-/GC]AAGTTTTAAGAAAAA | 55213 |
rs750956433 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546011 | GCTCTCCTGGCTACA[A/G]AGGAAAGGTAGAAAA | 55213 |
rs751060731 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562305 | GAAATTTCCCAGAAC[A/C]CAGATGGGAGAGAAC | 55213 |
rs751079361 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575958 | TCTGGGAGGCCAAGA[C/T]GAGCAGATCACAAGG | 55213 |
rs751079735 | snp | A/G | 3.34409e-05 | 0.00408893 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551308 | ACACAGTCCCAAGAC[A/G]TGGCACAGCCAAGTT | 55213 |
rs751115168 | snp | C/G | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534134 | GCTTCAGTTCTTAAA[C/G]GCTCCACATTTACTG | 55213 |
rs751116053 | in-del | -/AT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551958 | CTACTGAATTTTTCC[-/AT]TTTTTTTTTTTTTTT | 55213 |
rs751122118 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563610 | GTTACAGTGAGCTGA[G/T]ATCGTGCCACTGCAC | 55213 |
rs751123717 | snp | A/G | 1.66322e-05 | 0.00288371 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534273 | AAATCCTGGACACAC[A/G]ACAAAAATAAAAACA | 55213 |
rs751168977 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553677 | ACAGCAATGTAGGGC[A/G]GCAGACATAGACTGG | 55213 |
rs751198933 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534785 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 55213 |
rs751223960 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554400 | GAGGATATTCAACGG[C/T]CATCCCAAGGAATTC | 55213 |
rs751267261 | snp | G/T | 3.33067e-05 | 0.00408072 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555619 | GAGGAGTTGGTTGAT[G/T]TGCTGTAGAACCTGA | 55213 |
rs751301076 | snp | C/T | 4.98095e-05 | 0.00499022 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541813 | GACTGGAACATGGAT[C/T]GAAAATGCTCACACC | 55213 |
rs751311469 | snp | G/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582338 | TTAAAAATACAAAAA[G/T]TAGCTGGGCATAGTG | 55213 |
rs751388913 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571932 | TGTATACACTATCAA[G/T]CCAATAAACTAAAGC | 55213 |
rs751431603 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539564 | CAAGGAGGAGGAGCG[C/T]GGAGAGGCCCAGAGA | 55213 |
rs751433335 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542586 | TGTTTTTTGTTTTAC[A/G]TAATAAGCATATTCT | 55213 |
rs751451489 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558986 | ATGTATTAGTTTGCA[C/T]TTATTTAAATGTTTA | 55213 |
rs751497042 | snp | C/T | 1.66299e-05 | 0.00288352 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549620 | CTGCAGACGTGTGGG[C/T]AGAGTGACAGGCTGC | 55213 |
rs751529623 | in-del | -/AGA | 1.65162e-05 | 0.00287365 | cds-indel, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566629 | TTACCTTCGGTGCTG[-/AGA]AGAACATGTGGTCCA | 55213 |
rs751566216 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566746 | CCTAGACAGTTACTA[C/T]AGTTCAGTCCAAATA | 55213 |
rs751620467 | snp | A/G | 1.66488e-05 | 0.00288515 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551487 | CAAGTAAATTGAAAC[A/G]GTTACCATTAGCAGG | 55213 |
rs751656391 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547235 | ATAAAGTGAAAGGGA[A/G]TATTCAATTGGTTTC | 55213 |
rs751664258 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581329 | CTGCAACTGGCTGAA[C/T]GGGACAAGGAGCACT | 55213 |
rs751691216 | snp | A/C | 1.65636e-05 | 0.00287776 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567189 | ACAGTGCTTCACTGG[A/C]TGAGGTGCCGAAGAC | 55213 |
rs751740236 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569190 | TTGTGCAAAGTGCCT[A/G]TCTTTTTCTACTGGA | 55213 |
rs751781320 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539412 | CAGAGGCTTTTTCTG[C/T]AAACTTCCTAGGACA | 55213 |
rs751838221 | in-del | -/GTTCACACACACGCTGTGCAAAGCTGC | 1.6473e-05 | 0.00286988 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551471 | ACCGCAGACAATCTG[-/GTTCACACACACGCTGTGCAAAGCTGC]CAAGTAAATTGAAAC | 55213 |
rs751852190 | snp | C/T | 1.66018e-05 | 0.00288108 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559906 | AATAAAGAATAAAAG[C/T]AGCATACTTACCTCT | 55213 |
rs751852707 | snp | A/G | 9.09587e-05 | 0.00674322 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552218 | GCTGCCACTCTCACA[A/G]GGGTCAGCTGGTTGC | 55213 |
rs751936539 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556653 | CACGTATATACTGAG[C/T]GTGGCTTCCATGATT | 55213 |
rs751946246 | snp | A/G | 6.58913e-05 | 0.00573945 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559999 | CAAGAGATTGGTACA[A/G]ACCTGGACGGGAGCA | 55213 |
rs751967948 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536186 | TATGCAATAAATATT[C/T]AAAAGTTCCAAACAT | 55213 |
rs751971412 | snp | A/C | 3.31428e-05 | 0.00407066 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544868 | GTCTTCATGCTCTGA[A/C]GGCAACAAACATATA | 55213 |
rs752003345 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574969 | ACATTATGCTAATAA[A/G]TTAGACAAATATTGC | 55213 |
rs752008508 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546153 | CCCATCCAAAAAAAA[A/C]CCCACTTCTCATCAG | 55213 |
rs752050046 | snp | A/G | 5.09498e-05 | 0.00504701 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549467 | TCTTACCCACAGACA[A/G]GAGGCGCCACGAGAC | 55213 |
rs752063585 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547060 | AGGTTAAGTAGTATA[C/T]ACAAATCTGAAGATG | 55213 |
rs752112844 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534996 | CCGAGATCGCACCAC[C/T]GCACTCTAGCCTGGG | 55213 |
rs752186442 | snp | C/T | 1.6501e-05 | 0.00287232 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549540 | GAAGTGGGTGAGGTG[C/T]GGGAGGATCACGGAC | 55213 |
rs752188155 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553831 | AATTTGGCAATGGCT[A/C]TCAGTATTTCAAATG | 55213 |
rs752233948 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584815 | AATAAAAACAAAAGG[C/T]CACTTATGCGAGCAG | 55213 |
rs752238648 | snp | A/G | 1.75582e-05 | 0.0029629 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566803 | TTTTCTGAGTCTTTT[A/G]ACCGAAAGCTGTATT | 55213 |
rs752424028 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556618 | CCCCACCCTGCTTCA[C/T]GTGGCTGCAGGAGGT | 55213 |
rs752482129 | snp | A/G | 2.04463e-05 | 0.0031973 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541056 | GTATAATAATTTCCA[A/G]TACACAGAGATTTTG | 55213 |
rs752498548 | snp | A/C | 1.66023e-05 | 0.00288113 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541695 | AGCATCTTCTGGCGG[A/C]AGGTCGACTGTGTCT | 55213 |
rs752524516 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577143 | TTTACTTTATACTCT[A/G]AAAGCAAATTCAGTC | 55213 |
rs752539989 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572281 | GCAGTGAGCCGAGAT[C/G]ATGCCACTGCACTCC | 55213 |
rs752587795 | snp | A/G | 8.24341e-05 | 0.00641952 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551454 | TGCTAGAGTATGTGC[A/G]TAACCGCAGACAATC | 55213 |
rs752644104 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560533 | AGGGGAAAGAGATAG[A/C]CTGTTTACAAAGGAA | 55213 |
rs752714159 | snp | A/C | 1.65496e-05 | 0.00287655 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544859 | TGTTAAAAAGTCTTC[A/C]TGCTCTGAAGGCAAC | 55213 |
rs752738528 | snp | C/T | 1.66902e-05 | 0.00288874 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560117 | ACAAAAAATCAGCTC[C/T]AAAAAGAAATAGTAA | 55213 |
rs752767485 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556894 | CATAAATTAGCAAGT[C/T]TGAGCTAATTTCAGC | 55213 |
rs752811095 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560873 | AACAGCCAAATGGGG[G/T]AGACACACAGGGTAA | 55213 |
rs752816591 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546865 | ACCCAGTTAATAACA[A/G]GCCACGGACCAGTAC | 55213 |
rs752823813 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570101 | TCAAGTTAGCCTTCA[A/C]AATGTTTAATTTTAC | 55213 |
rs752945738 | in-del | -/CATCATTGTC/CATCATTGTCAGTAACGTACAGTGCTTCACTGGCTG/CATCATTGTCAGTAACGTACAGTGCTTCACTGGCTGAGGTGCCGA | 4.995e-05 | 0.00499731 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49566770 | CAAATACAAAGACCT[lengthTooLong]AGAAAATAGATAGTT | 55213 |
rs752976296 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547331 | TGGGACAACTCCACC[C/T]GTCTGACACACCTAA | 55213 |
rs753026933 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576328 | AATGGTAAATTTTAC[A/G]CTATATACCTTTTAC | 55213 |
rs753045254 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548833 | AATTAACGTATAAGG[A/G]CTTTCTTCTGGGGTG | 55213 |
rs753095236 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534266 | TTCTTCTAAATCCTG[A/G]ACACACAACAAAAAT | 55213 |
rs753110317 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553620 | ACAAATAAAGGCCTT[A/G]CTCAAATTACAAACC | 55213 |
rs753135717 | snp | C/T | 1.65403e-05 | 0.00287574 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555595 | TATGTAAACAGTTTG[C/T]AACTTTTCGAGGAGT | 55213 |
rs753137465 | in-del | -/AC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574698 | TAAAAAAAAAAAAAA[-/AC]ACATTAGAATTATAT | 55213 |
rs753192744 | snp | A/G | 1.67192e-05 | 0.00289125 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559885 | ACTATGATGAAAAAA[A/G]AAAAGAATAAAGAAT | 55213 |
rs753276387 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542952 | TATTTTAAAGTGAGA[C/T]ACGGCACAAAGAGAA | 55213 |
rs753371757 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586680 | GTTCATTCTTTTGTC[C/T]GTATCTGAAATGTCC | 55213 |
rs753376950 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555455 | CATTCACCTTGTGAA[A/G]AAACTGACGTGTAAT | 55213 |
rs753398890 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548907 | AGGCACAGTGGCAGG[G/T]GGATCACCTGAGGTC | 55213 |
rs753413636 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572490 | AATATAAATGTAGTT[A/C]AACTAAATTTCATTT | 55213 |
rs753422733 | snp | A/T | 6.61507e-05 | 0.00575074 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560084 | GCATAAACCACTCCA[A/T]CTGTGCACACAAAGC | 55213 |
rs753443658 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533238 | TAATTTAGGAAGGCA[A/G]GAGTATACTATACAT | 55213 |
rs753494384 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533920 | AAAATACACTTATCT[A/G]GAAACAAGGGTTGTT | 55213 |
rs753560745 | snp | A/G | 1.65449e-05 | 0.00287614 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551479 | ACAATCTGCAAGTAA[A/G]TTGAAACGGTTACCA | 55213 |
rs753572158 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565035 | CCCGCTCCCTCTCCC[C/T]CTCTTTCCACGGTCT | 55213 |
rs753655433 | snp | C/G | 1.65015e-05 | 0.00287237 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540878 | TTGTTTAAGTTACCT[C/G]TGCATCATATCTGAC | 55213 |
rs753655600 | snp | C/G | 0.000170054 | 0.00921943 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552203 | CACACGCTGTGCAAA[C/G]CTGCCACTCTCACAG | 55213 |
rs753681222 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560747 | GAAGATTAAAAGGCT[A/G]GAGATGACTTGAGAG | 55213 |
rs753718719 | snp | A/C | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581400 | CTGAGCTTGAGTGAG[A/C]GAGAACTGTGCTGCC | 55213 |
rs753745692 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551902 | GAGACTCCGTCTCAA[-/A]AAAAAAAAAAAAAAA | 55213 |
rs753841046 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539472 | CCAGCAACTTGAGCC[A/G]AGACATCTGCCTCTG | 55213 |
rs753856950 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571112 | AGCACTTTGAGAGGC[C/T]GAGGCGGGCGGACCA | 55213 |
rs753964381 | snp | C/T | 9.89674e-05 | 0.00703377 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555571 | AGGCAATGCCAACTA[C/T]CCTCTTAATATGTAA | 55213 |
rs754022607 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548882 | TTGACATAAAGGGTG[A/G]ATGTAGGCCAGGCAC | 55213 |
rs754060684 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560475 | CAAATACCAAGTCAC[A/G]GGGAACCCACAGGGG | 55213 |
rs754068865 | in-del | -/AAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574685 | AGATGGTGATTCCTT[-/AAA]AAAAAAAAAAAACAT | 55213 |
rs754104549 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536360 | AGAGTCGCACAGTCA[A/C]GCTGAACCACTTAGC | 55213 |
rs754222190 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577821 | AGCTACAGCAAGCTT[G/T]AAACTACTCAAAACA | 55213 |
rs754243839 | snp | C/T | 1.66239e-05 | 0.00288299 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534105 | AGCACTCACACAGAA[C/T]CCAGCAGCCTTGCGC | 55213 |
rs754248070 | in-del | -/GA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544288 | AACCTGACCAACATG[-/GA]GAGAAACCCCATCTC | 55213 |
rs754342178 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578171 | AGTCCCTGATAGAAA[A/G]TGGCATAGTATTTGC | 55213 |
rs754397059 | in-del | -/TCTTCTGGCGGCAGGTCGACT | 1.72892e-05 | 0.00294012 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541012 | CCAGAAGACCTAAAA[-/TCTTCTGGCGGCAGGTCGACT]GTAAAATATGTGAAA | 55213 |
rs754407540 | snp | A/G | 0.000134226 | 0.00819115 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549478 | GACAGGAGGCGCCAC[A/G]AGACGGCGGGAGTGG | 55213 |
rs754421292 | in-del | -/GA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539566 | AGGAGGAGGAGCGTG[-/GA]GAGGCCCAGAGAGGA | 55213 |
rs754486487 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553699 | ATAGACTGGGGCTTT[A/T]CAGGGTAACATGATG | 55213 |
rs754573796 | snp | A/C | 1.65921e-05 | 0.00288024 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560094 | CTCCATCTGTGCACA[A/C]AAAGCACACAAAAAA | 55213 |
rs754645631 | snp | A/G | 1.6498e-05 | 0.00287206 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549516 | GGCAAACACGTCGTC[A/G]GTGCAGGAGAAGTGG | 55213 |
rs754722945 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570663 | ACAGAGGCAGTAATA[C/T]TGGCCAAGCAAGTAA | 55213 |
rs754885557 | snp | C/T | 3.54258e-05 | 0.00420852 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541021 | CCTAAAAGTAAAATA[C/T]GTGAAAGGTTTAATC | 55213 |
rs754915252 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577050 | CCTACAGATCAATAT[-/C]CCATTCCCTGGGATG | 55213 |
rs754934203 | snp | A/G | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549274 | GAGAGAAAATTTAAA[A/G]TTCATGGTAATATTT | 55213 |
rs754970640 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559423 | GCACTTTTGGAGGCC[A/G]AGGCGGGCAGATCAC | 55213 |
rs755061078 | snp | C/T | 3.56608e-05 | 0.00422245 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541872 | TTCAGCAGCAATTTT[C/T]AAAAAAGAAAAAAAA | 55213 |
rs755096486 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555783 | ATGAGTACTTAAGAT[A/G]TGCTAAACGGTTCTA | 55213 |
rs755097444 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562516 | AGAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 55213 |
rs755099588 | in-del | -/AGA | 0.000324928 | 0.012742 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551520 | ACAGGAAGGGCAGGG[-/AGA]AGAACATCTACTTAA | 55213 |
rs755193161 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566675 | GGCTTTTAATCTTCT[C/T]TCCACATAAGCCTTC | 55213 |
rs755340992 | snp | A/T | 0.000133473 | 0.00816817 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567329 | GACATCTCTGCTGGA[A/T]CAGAAAGGATTCCAG | 55213 |
rs755368102 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546241 | TGGCAACAAGTATAG[C/T]ACATCCTTTCAGAGA | 55213 |
rs755424993 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547074 | ATACAAATCTGAAGA[C/T]GTGTACAGAAGTGCT | 55213 |
rs755428749 | snp | A/G | 4.96463e-05 | 0.00498203 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555488 | AAAAAGAAGGTAGAA[A/G]GGGAAATGGGAGTGG | 55213 |
rs755449340 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580492 | ACTCAAGAGGCTGAG[A/G]TGGGAGGATCACCTG | 55213 |
rs755482160 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535139 | ACTTCCACCACACTA[A/G]TATCTCAGAACATCA | 55213 |
rs755518574 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544435 | GATCGTGCCACTGCA[-/C]TCCAGCCTGAGCAAC | 55213 |
rs755520846 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558420 | AAAGTAGGCTTGTCA[A/T]GGTGGCTATGCCTGT | 55213 |
rs755546895 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541740 | GAGAAAGGCACGATA[C/T]ACTGGGTAAGAAAAC | 55213 |
rs755561224 | in-del | -/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545482 | ACACCTACATGAAGG[-/G]AACAGTTTTATAAGA | 55213 |
rs755599146 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541521 | ATTAACCATAATAAC[G/T]ACACAATACTACTTT | 55213 |
rs755622975 | snp | A/G | 1.65345e-05 | 0.00287524 | splice-donor-variant | RCBTB1 | GRCh38.p7 | 13:49559916 | AAAAGCAGCATACTT[A/G]CCTCTCCATCAGCTG | 55213 |
rs755701981 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583687 | GAGTAGCTGGGACTA[C/T]AGGCGCACACCACCA | 55213 |
rs755752740 | snp | G/T | 0.000116301 | 0.00762477 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544896 | ATATTAATATGGCAA[G/T]TTCAAGGAACAGATT | 55213 |
rs755781987 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584840 | GAGCAGAACACAGCG[C/T]GCTCGATAGTCATCT | 55213 |
rs755819513 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571374 | AGTATCCACTCTCCC[A/T]ATAAAAAGCATTCCG | 55213 |
rs755863648 | snp | A/G | 3.29728e-05 | 0.00406021 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551346 | TTTCTCCACCATGAT[A/G]TGTGCTGGGCTTAGC | 55213 |
rs755869009 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559230 | GGAATGAAGAGAATC[C/G]TATCATATGGTACAA | 55213 |
rs755976325 | in-del | -/CACAGACAGGAGGCGCCACG | 3.31345e-05 | 0.00407016 | splice-acceptor-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544864 | AAAGTCTTCATGCTC[-/CACAGACAGGAGGCGCCACG]TGAAGGCAACAAACA | 55213 |
rs755990823 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582518 | ATAAATAAATGCAAG[-/A]GAAACTGTAGAAAGG | 55213 |
rs756000111 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551597 | GACTGACATTTGCTG[C/G]AACATTAAAAAAGCA | 55213 |
rs756054399 | snp | A/G | 3.3493e-05 | 0.00409211 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534292 | AAAATAAAAACAAAA[A/G]TGGCTTTTTTAGGCA | 55213 |
rs756073261 | snp | A/T | 8.26112e-05 | 0.00642641 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540870 | TCTGTTTGTTGTTTA[A/T]GTTACCTCTGCATCA | 55213 |
rs756185482 | in-del | -/AG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563336 | CTGCCTGGGTGACAG[-/AG]AGAGAGAGACCCTGC | 55213 |
rs756269937 | snp | A/C | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541729 | TAGAGGTACTGGAGA[A/C]AGGCACGATACACTG | 55213 |
rs756310504 | snp | C/G/T | 5.05824e-05 | 0.00502882 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566571 | AAGCTTAGAATTAAC[C/G/T]GGTCAATTTCTTACA | 55213 |
rs756516573 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563779 | ACCACATGATGATGC[C/T]CAGATTTGGATTTCA | 55213 |
rs756536896 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536216 | TTAAAAGCCAAACTA[A/G]AGAATTCTGAAAACA | 55213 |
rs756593798 | snp | C/G | 0.000151392 | 0.00869901 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567135 | CCTAAAACGAAACTA[C/G]GTTTCAAGAGACTCT | 55213 |
rs756627995 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537720 | TATCTTGAAACAATG[-/T]TTTATCCACATTTTC | 55213 |
rs756679161 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553923 | TACAAAGATACACAT[A/G]CACAGAGTAACATAG | 55213 |
rs756695751 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574849 | ATCCAAATATCCATG[A/G]ACAGATGAATGGATA | 55213 |
rs756704443 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544240 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCACCTGA | 55213 |
rs756731394 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560008 | GGTACAGACCTGGAC[A/G]GGAGCAATGCCTTGG | 55213 |
rs756742097 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532060 | CAAGAGTACATTTAG[A/G]GCTATCTTAAGAAAT | 55213 |
rs756775673 | snp | A/C | 1.66407e-05 | 0.00288446 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534275 | ATCCTGGACACACAA[A/C]AAAAATAAAAACAAA | 55213 |
rs756868342 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583096 | GGATCACTTGAGCCT[-/G]GGAGTTTGAGGCTGC | 55213 |
rs756913735 | snp | C/T | 1.65765e-05 | 0.00287888 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559909 | AAAGAATAAAAGCAG[C/T]ATACTTACCTCTCCA | 55213 |
rs756922151 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581466 | GTGATGAGTCCTACT[A/G]TGGACATTTGTGCCA | 55213 |
rs756973518 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560755 | AAAGGCTGGAGATGA[C/T]TTGAGAGTTGAGGAC | 55213 |
rs757010319 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579675 | ATGCCCTGAATGCTT[C/G]ACTAAGGAGTCTGAG | 55213 |
rs757069624 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551640 | GCGTGGTGGCTCATG[A/C]CTGTAATCCCAGCGC | 55213 |
rs757090075 | in-del | -/TTAAAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573762 | GCCTTCTTTGTATTT[-/TTAAAA]TATAGTCCCAAATTT | 55213 |
rs757124685 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552736 | TAGGAAGAAAGATTA[A/G]GGAAGACTTTTCAAA | 55213 |
rs757148365 | snp | A/G | 1.65877e-05 | 0.00287986 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551320 | GACGTGGCACAGCCA[A/G]GTTACCTTTCTTTCT | 55213 |
rs757209150 | snp | A/G | 1.66563e-05 | 0.0028858 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549624 | AGACGTGTGGGCAGA[A/G]TGACAGGCTGCAATC | 55213 |
rs757261558 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534159 | TTACTGGCTTTAGCA[A/G]TGAATTCCTTTAGCA | 55213 |
rs757279580 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547927 | TGAGTAGCTGATACT[A/G]CAGGCAGGCACCACC | 55213 |
rs757281514 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558815 | ATCGTTTGCTTTTGA[A/G]CTGTGTGGCAGTAGG | 55213 |
rs757297898 | in-del | -/TAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535078 | ACTTTTATGCTCTCC[-/TAA]TAATGACTTTATTTT | 55213 |
rs757322383 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539563 | ACAAGGAGGAGGAGC[A/G]TGGAGAGGCCCAGAG | 55213 |
rs757394822 | snp | G/T | 1.66618e-05 | 0.00288628 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551488 | AAGTAAATTGAAACG[G/T]TTACCATTAGCAGGA | 55213 |
rs757404827 | snp | C/G | 3.88583e-05 | 0.00440768 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552226 | TCTCACAGGGGTCAG[C/G]TGGTTGCCATTGTTT | 55213 |
rs757421190 | snp | C/T | 1.73486e-05 | 0.00294517 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541633 | ATATGAGGGGATATA[C/T]TCTCCACCATGCGGC | 55213 |
rs757465477 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572971 | TTCCCTGACAGTCAA[A/G]TACCTTGGTAAGTAC | 55213 |
rs757547686 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576875 | TAAAGATAAAACAAG[G/T]GTGCAAGGAAAGAAA | 55213 |
rs757573944 | snp | A/G | 3.31477e-05 | 0.00407096 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544869 | TCTTCATGCTCTGAA[A/G]GCAACAAACATATAT | 55213 |
rs757579708 | in-del | -/AAAGTGAAAGATGAT | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533070 | AACAGAGGAAAACCA[-/AAAGTGAAAGATGAT]AAAGTGAAAGATGAT | 55213 |
rs757654396 | in-del | -/GTCGAC | 1.73754e-05 | 0.00294744 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541013 | CAGAAGACCTAAAAG[-/GTCGAC]TAAAATATGTGAAAG | 55213 |
rs757731464 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545004 | CCTTGTTTGACAAAT[C/G]AATTCTACGGTATTA | 55213 |
rs757780948 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572329 | GAGACTCTGTCTCAG[-/A]AAAAAAAAAAAAAAT | 55213 |
rs757803994 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560909 | GCGGGGATGAGGGGT[A/G]CACGGAGCTCCCATG | 55213 |
rs757819365 | in-del | -/TTAAGGCAAGC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547254 | TCAATTGGTTTCACT[-/TTAAGGCAAGC]TTAACTCTTCCTAAG | 55213 |
rs757860769 | snp | A/G | 1.68653e-05 | 0.00290385 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567128 | AATAAGTCCTAAAAC[A/G]AAACTAGGTTTCAAG | 55213 |
rs758090303 | snp | A/G | 1.65351e-05 | 0.00287528 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555499 | AGAAAGGGAAATGGG[A/G]GTGGAGACACCTCAC | 55213 |
rs758248818 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539795 | CTGCAGACAAAGTCA[C/G]CTACATTTGACCTTA | 55213 |
rs758253525 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570515 | GCCTGTGTCCCAGGT[C/T]TGCTTTTAAAATCAG | 55213 |
rs758349225 | in-del | -/CGT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566775 | ACAAAGACCTAGAAA[-/CGT]ATAGATAGTTTTTTT | 55213 |
rs758367790 | in-del | -/GTAAGT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583312 | AGAAAGCTGGAGACC[-/GTAAGT]CTTTAGAGGTACCCA | 55213 |
rs758406575 | snp | A/C | 5.00973e-05 | 0.00500461 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560119 | AAAAAATCAGCTCCA[A/C]AAAGAAATAGTAACC | 55213 |
rs758420965 | snp | A/G | 1.65034e-05 | 0.00287253 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549541 | AAGTGGGTGAGGTGC[A/G]GGAGGATCACGGACT | 55213 |
rs758434186 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578045 | AAATCTAAAGGGCCT[C/T]GGAAAAAAGTACTAT | 55213 |
rs758449052 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536651 | GACCAGGAGATGAAC[A/T]AAGTTCCCGACAGAA | 55213 |
rs758467644 | in-del | -/A | 0.00178096 | 0.0297877 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541879 | CAATTTTTAAAAAAG[-/A]AAAAAAAAATTACCT | 55213 |
rs758477566 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549889 | ATAGATCACACAGAC[C/G]GCCGAGGAAAACTTG | 55213 |
rs758522635 | in-del | -/GGTT | 1.70632e-05 | 0.00292084 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549654 | TCTACCACCCTGAAA[-/GGTT]AGTTTTAAGAAAAAT | 55213 |
rs758542092 | snp | A/G | 1.68709e-05 | 0.00290434 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567125 | CCAAATAAGTCCTAA[A/G]ACGAAACTAGGTTTC | 55213 |
rs758552781 | snp | A/T | 1.66843e-05 | 0.00288823 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566773 | AATACAAAGACCTAG[A/T]AAATAGATAGTTTTT | 55213 |
rs758613769 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551393 | CAGTTCCCAGCTGCC[C/T]ATATGTGTTAGCTCC | 55213 |
rs758630299 | snp | C/T | 1.65523e-05 | 0.00287678 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551481 | AATCTGCAAGTAAAT[C/T]GAAACGGTTACCATT | 55213 |
rs758791880 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555509 | ATGGGAGTGGAGACA[C/T]CTCACCTCGCCATTG | 55213 |
rs758794255 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534705 | GAAACAGAAAGGTAA[C/T]GAAGAGATATGGTCA | 55213 |
rs758804412 | in-del | -/AAGGG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551103 | GACTCTGTCTCAAAA[-/AAGGG]AAGGGAAGGGAAGGG | 55213 |
rs758815759 | snp | C/T | 6.81477e-05 | 0.00583688 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544708 | AGAAAAGTCAAGTTA[C/T]TGATGTCTCTGAGCT | 55213 |
rs758833226 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556559 | GGTGTTGGCAGTAGA[A/G]GAAATAATTTCCTCC | 55213 |
rs758841272 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544295 | ACCAACATGGAGAAA[A/C]CCCATCTCTATTATA | 55213 |
rs758844395 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560942 | CTCCCTGGCATGCCA[A/C]CCCCTCCCAGCACCT | 55213 |
rs758857044 | snp | C/T | | | synonymous-codon, missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559921 | CAGCATACTTACCTC[C/T]CCATCAGCTGCCAGA | 55213 |
rs758949156 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573651 | GACGGGGTTTCACCA[C/T]GTTTGCCAGGCTGGT | 55213 |
rs758974477 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578568 | ACTAGAATGCAAATA[C/T]AACTGGAATAATTAA | 55213 |
rs758985746 | snp | A/G | 1.65173e-05 | 0.00287374 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541796 | TGTCTTCATTCCAAT[A/G]CGACTGGAACATGGA | 55213 |
rs759004113 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539144 | GTGCCGGGATTACAG[A/G]CGTGATCTCCAAGCC | 55213 |
rs759028358 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546044 | TCTCAAAAGTCAGGC[C/T]TCCCCTGACCTTGCA | 55213 |
rs759041552 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577545 | GCTGTTATGTACTGG[C/T]TTTTAAATGCCACCA | 55213 |
rs759059131 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541343 | TAATACCTAGGTGAT[A/G]GGTTGACAGGTACAG | 55213 |
rs759113467 | snp | C/T | 3.30666e-05 | 0.00406598 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549595 | TACACGTGCCCACCC[C/T]GCGTCTTGGCTGCAG | 55213 |
rs759208589 | in-del | -/GTTT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573352 | TTCTTTAGTTTGTTC[-/GTTT]GTTTGTTTTCGTCAG | 55213 |
rs759212043 | snp | A/G | 0.000149772 | 0.00865236 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567268 | GATGGGCCACTTTCC[A/G]ACATCCACCATGACT | 55213 |
rs759243269 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554401 | AGGATATTCAACGGC[A/C]ATCCCAAGGAATTCT | 55213 |
rs759249015 | snp | A/T | 1.64985e-05 | 0.0028721 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566637 | GGTGCTGAGAAGAAC[A/T]TGTGGTCCACTCCCG | 55213 |
rs759266417 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566710 | TTTTTGGGTACAAGT[A/G]TACTCTGGTTATCTC | 55213 |
rs759268180 | in-del | -/TTCTC | 1.6593e-05 | 0.00288031 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534269 | TCTAAATCCTGGACA[-/TTCTC]CACAACAAAAATAAA | 55213 |
rs759286286 | snp | A/G | 5.15477e-05 | 0.00507653 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552206 | ACGCTGTGCAAAGCT[A/G]CCACTCTCACAGGGG | 55213 |
rs759397614 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543924 | ACTCCTAGGATCAAG[C/T]GATATTCCCGCCTTG | 55213 |
rs759419416 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586311 | TGCTCCAGCCTATCA[C/T]CTATAAAGACTACAG | 55213 |
rs759419867 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572132 | AGAAGTTTGAGACCA[G/T]CCTAGATGACATGGT | 55213 |
rs759493986 | snp | A/T | 1.73576e-05 | 0.00294593 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559870 | ATGTTAAGTGTATTT[A/T]CTATGATGAAAAAAA | 55213 |
rs759533533 | snp | C/T | 5.0234e-05 | 0.00501144 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541679 | CTACCACAGTACCTA[C/T]AGCATCTTCTGGCGG | 55213 |
rs759550970 | in-del | -/TTTG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542458 | AGATTTTTTTGCTCC[-/TTTG]TTTTTTTTAAAATGA | 55213 |
rs759617958 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573184 | TTAGCTTAGCTATGT[A/T]ATAAAACAATATGTC | 55213 |
rs759625723 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581963 | ACCATGAGTATAAAC[A/G]ACTTGTTCAAGAAAT | 55213 |
rs759647714 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585027 | CAGCACTACTCTCAG[A/G]AGACGAAGGAGAGAT | 55213 |
rs759656755 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552532 | TCCTGTTTAATACAT[A/G]AGGAAGTTGAGCCTC | 55213 |
rs759657278 | in-del | -/TA | 1.64889e-05 | 0.00287126 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566652 | TGTGGTCCACTCCCG[-/TA]TAACTGAGGCTTTTA | 55213 |
rs759665055 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563258 | ATTTAAAAATGAGGT[A/G]GGAAGATCGCTTGAG | 55213 |
rs759771820 | snp | C/G | 3.31967e-05 | 0.00407397 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534110 | TCACACAGAACCCAG[C/G]AGCCTTGCGCTTCAG | 55213 |
rs759798160 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570991 | CCTAAAGTCACTTCT[A/T]TCTGACTTTATCTTG | 55213 |
rs759809197 | snp | A/C | 1.65362e-05 | 0.00287538 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544852 | CTGCAACTGTTAAAA[A/C]GTCTTCATGCTCTGA | 55213 |
rs759821948 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582790 | GGTTTTGATTGGCAT[G/T]TGGAGACCATTCTCT | 55213 |
rs759871231 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570031 | AAGCCATACAAGCAG[A/G]TAAGTAAATTTCAAG | 55213 |
rs759900534 | in-del | -/AT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544183 | TTAATTTAAAAAACA[-/AT]ATAAGCTGGGCGTGG | 55213 |
rs759902705 | snp | C/T | 1.78442e-05 | 0.00298694 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549427 | GGTAGTACCATTCTT[C/T]CTGGGTGGAGGTGGC | 55213 |
rs759941855 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553590 | AATAGCCATAGGAAA[A/C]AGTACTGACCAGGAA | 55213 |
rs760005300 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576118 | CATGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 55213 |
rs760059462 | snp | C/T | 1.65176e-05 | 0.00287376 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534257 | AAAGCAGAATTCTTC[C/T]AAATCCTGGACACAC | 55213 |
rs760108164 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556260 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 55213 |
rs760108178 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576346 | ATATACCTTTTACCC[A/C]AATTTTTTAAAATCA | 55213 |
rs760119701 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538394 | AGTCAATTACGTAAC[C/T]TGTATTGTAACCTAA | 55213 |
rs760182143 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567803 | AGGTATCATACCACA[A/C]ATTCAATGAGGATTA | 55213 |
rs760182251 | snp | C/G | 1.69146e-05 | 0.0029081 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541001 | ATGTCGCCAAATCCA[C/G]AAGACCTAAAAGTAA | 55213 |
rs760211901 | snp | C/T | 5.07704e-05 | 0.00503812 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541662 | GCTCGTCCATCCCAA[C/T]GCTACCACAGTACCT | 55213 |
rs760231312 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538685 | CACACCACTGTGCTT[C/T]AGCCTGGGCAACAGA | 55213 |
rs760255645 | in-del | -/AAGGG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551107 | TGTCTCAAAAAAGGG[-/AAGGG]AAGGGAAGGGAAGGG | 55213 |
rs760289196 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586489 | TTTCTAAATATCACC[A/G]GATAACTTCACTTTT | 55213 |
rs760431080 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545280 | TTCAAGGGGTCAGCA[C/T]ACCCAACTCAAGGAG | 55213 |
rs760484853 | in-del | -/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546621 | TGGACGGCCCCATCT[-/G]GGGGTGATGGGAGAC | 55213 |
rs760488283 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533850 | AAGAAGACCAAAAAC[A/G]ACTAACTTTCACCCT | 55213 |
rs760525233 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574292 | CCTGGCTAATTTTTG[G/T]ATTTTTAGTAGAGAC | 55213 |
rs760539303 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534595 | TTATGCTCAAAGACA[C/T]TGTTGTAAAAGGCAG | 55213 |
rs760572901 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548427 | AAAGTTCATCTTTGA[C/T]TGGTATTATATCAAG | 55213 |
rs760586046 | snp | A/G | 4.94866e-05 | 0.00497402 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551460 | AGTATGTGCGTAACC[A/G]CAGACAATCTGCAAG | 55213 |
rs760590355 | snp | C/T | 4.98078e-05 | 0.00499013 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567161 | ACTCTTACCTCATCA[C/T]TGTCAGTAACGTACA | 55213 |
rs760659825 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573821 | CAGAGCCTCGCTCTG[C/T]TGTCCAGTCTGGAGT | 55213 |
rs760700601 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49531995 | GTTCTAAATATTACA[C/T]AAATACAGCTTACAT | 55213 |
rs760723441 | in-del | -/ATCCTTC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543789 | TACTGGGCTCAAGCA[-/ATCCTTC]ATCCTTCCACCTCAG | 55213 |
rs760810275 | snp | C/T | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540526 | GGAAAGACAGCAAGG[C/T]AAGTCTCGAAATAAA | 55213 |
rs760860572 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582208 | GTGCAACAGAAGCGC[C/T]GGGCGCAGTGGCTCA | 55213 |
rs760886273 | snp | C/T | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531585 | CTCACTCATCCGCCA[C/T]TCACCTCCCGCTGTG | 55213 |
rs760901432 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549509 | CAAAGCAGGCAAACA[C/T]GTCGTCGGTGCAGGA | 55213 |
rs760947101 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580268 | ACAGAACAAAAAAAC[C/G]AATGATGGGTCAAAG | 55213 |
rs760959033 | snp | A/T | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555551 | CATGGATGAAGTCTG[A/T]CCACAGGCAATGCCA | 55213 |
rs761026380 | snp | A/G | 1.66048e-05 | 0.00288134 | stop-gained, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541814 | ACTGGAACATGGATC[A/G]AAAATGCTCACACCT | 55213 |
rs761045887 | snp | A/C | 3.69706e-05 | 0.0042993 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555691 | ACAAGAGAAAGAAAA[A/C]GGAAAAGGAAAGAAT | 55213 |
rs761053001 | snp | G/T | 1.65537e-05 | 0.0028769 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566619 | GGTTCCCTCCTTACC[G/T]TCGGTGCTGAGAAGA | 55213 |
rs761135620 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577772 | GAATGTTGGAACAAT[A/C]ATTTTAAGTAGCCTA | 55213 |
rs761152958 | in-del | -/GC/GCATCTTCTGGCGGC | 3.44912e-05 | 0.00415267 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541011 | TCCAGAAGACCTAAA[-/GC/GCATCTTCTGGCGGC]AGTAAAATATGTGAA | 55213 |
rs761186314 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572102 | GAGGTAGAGGCAGGC[A/G]GATCACTTGAGTCCA | 55213 |
rs761214206 | snp | A/G | 4.9561e-05 | 0.00497775 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549585 | GCCCCACATGTACAC[A/G]TGCCCACCCTGCGTC | 55213 |
rs761228187 | snp | A/T | 3.33067e-05 | 0.00408072 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534093 | ACAGTGCCCCAGAGC[A/T]CTCACACAGAACCCA | 55213 |
rs761341486 | snp | C/G | 7.24611e-05 | 0.00601875 | splice-donor-variant | RCBTB1 | GRCh38.p7 | 13:49552177 | AGTGCACCACACGTA[C/G]CTGGTTCACACACAC | 55213 |
rs761397358 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533963 | AAGAAAAGCCGTACA[C/T]CCTTGTTATGTTCCT | 55213 |
rs761412864 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574726 | TATTATCTAGATAAA[C/T]TCCATTTCTAGCATA | 55213 |
rs761507336 | in-del | -/AGT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559360 | AACTCAAAGAAACAG[-/AGT]AGTAGAAAGTTGTTG | 55213 |
rs761528210 | snp | C/T | 3.30759e-05 | 0.00406655 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540863 | TCTGGTTTCTGTTTG[C/T]TGTTTAAGTTACCTC | 55213 |
rs761593909 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534749 | CATTAAAAAGAAAAT[A/C]CCAGCCGGGCACGGT | 55213 |
rs761617866 | snp | C/T | 1.66588e-05 | 0.00288602 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540990 | TTCACAGTAAGATGT[C/T]GCCAAATCCAGAAGA | 55213 |
rs761642667 | snp | C/T | 9.9167e-05 | 0.00704086 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544798 | TTCGAAACTTCAGAT[C/T]AGCAGTTTCTGGACT | 55213 |
rs761644082 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566747 | CTAGACAGTTACTAT[A/G]GTTCAGTCCAAATAC | 55213 |
rs761667719 | in-del | -/AAATAAATAAATA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566292 | AATAAATAAATAAAT[-/AAATAAATAAATA]AAAAAGTTGCATTGC | 55213 |
rs761670182 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563447 | ATGGGTGGATCACCT[C/G]AGGTCGGGAGTTCAA | 55213 |
rs761753914 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532137 | CAAATAAGAGTTGTC[A/G]TATCCTGCTATGATT | 55213 |
rs761790974 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543742 | ATCTCACTCTGTCTC[C/G]CAGGATGATCACAGC | 55213 |
rs761814597 | in-del | -/A | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549253 | AATTGAAATGAAAGC[-/A]CTTATGAGAGAAAAT | 55213 |
rs761824838 | snp | A/T | 3.30164e-05 | 0.00406289 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549566 | CGGACTGACCCCGGC[A/T]CTGGCCCCACATGTA | 55213 |
rs761879570 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546345 | AGGGAAAAAACACTT[C/T]TGACTTTCAGTGGGT | 55213 |
rs761902294 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553427 | AAGGAGTGATAGGGG[A/G]ATCATGAGAGGGAAA | 55213 |
rs761957743 | in-del | -/GCAGGT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543026 | CTTTGGGAGGCCGAG[-/GCAGGT]CAGCCTCAATCACCT | 55213 |
rs761977782 | snp | A/T | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531670 | GGACCCCTGACCTAA[A/T]GGACTCTTCATCTTG | 55213 |
rs762032989 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532661 | ATCTTTAGGGCCTCA[C/T]TCCCCTTCCCACCCC | 55213 |
rs762084547 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549791 | CTGCCAAGTCACAGC[A/C]ACAAAAGCAACAGAT | 55213 |
rs762102785 | snp | G/T | 5.54216e-05 | 0.00526381 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552316 | AGGGAGAGAGTGAGA[G/T]TTTTAAACTGCTGGT | 55213 |
rs762112398 | snp | G/T | 1.66568e-05 | 0.00288585 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567302 | GCTTCAAGCAATTCC[G/T]ATAAATAAGCCGACA | 55213 |
rs762140892 | in-del | -/TCG/TCGGTGCTGAGAAGAACATGTGGTCCACTCCCGTAACTGAG | 6.61807e-05 | 0.00575209 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49560086 | TAAACCACTCCATCT[lengthTooLong]GTGCACACAAAGCAC | 55213 |
rs762149652 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560239 | GACAGAGTAAAGGAG[A/G]GAGAGATGGGTGACA | 55213 |
rs762197971 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587531 | AGTATTATGATACAA[A/G]GTGCTAAGTGAACAC | 55213 |
rs762219254 | in-del | -/AATGAATGAATG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558354 | ACAAACGGGTTGGAA[-/AATGAATGAATG]AATGAATGAATGAAT | 55213 |
rs762220990 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537930 | TTAATGTGTGTACAT[C/T]TGCTTCAAAGCTATC | 55213 |
rs762228869 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579058 | TTACCAATTTCTTAC[A/G]TATAATTCTGATGGG | 55213 |
rs762238209 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539262 | AGCGCCAGCTCCATG[C/T]CCACACTGTGACAGA | 55213 |
rs762278236 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580605 | AAAGAAAAAAGAAAT[A/G]GATAAAACATAATAC | 55213 |
rs762289480 | snp | A/C | 3.29533e-05 | 0.00405901 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560042 | GTCGTCCCATTCCCA[A/C]GCTGGCTATATCCAT | 55213 |
rs762289572 | snp | A/G | 1.69453e-05 | 0.00291073 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549470 | TACCCACAGACAGGA[A/G]GCGCCACGAGACGGC | 55213 |
rs762312243 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543675 | CATAGGTCCCTCACA[G/T]TTATACAAGGAACTA | 55213 |
rs762366981 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564201 | TCTTTCAATATGGCA[A/G]CTACATGAATGCCAG | 55213 |
rs762382848 | in-del | -/TTTCTTTCTCCACCA | 1.69772e-05 | 0.00291347 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49549649 | CAATCTCTACCACCC[-/TTTCTTTCTCCACCA]TGAAAAGTTTTAAGA | 55213 |
rs762447081 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535888 | ATTAGCCAGGTGTGG[C/T]GGCAAGCACCTGTAA | 55213 |
rs762492479 | snp | C/T | 1.74821e-05 | 0.00295647 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566801 | TTTTTTCTGAGTCTT[C/T]TGACCGAAAGCTGTA | 55213 |
rs762610170 | snp | A/C | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555535 | CATTGTCCAGAACAG[A/C]CATGGATGAAGTCTG | 55213 |
rs762637010 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553536 | CTGCTGAAAGTAACA[C/G]AGCTAGGCATAGGTT | 55213 |
rs762656320 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563588 | TGCTTGAACCCAGGA[A/G]GCTGATGTTACAGTG | 55213 |
rs762662633 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577369 | TATGGAGATTTTAAA[A/T]ACAACAGGAAATGGA | 55213 |
rs762753877 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553697 | ACATAGACTGGGGCT[C/T]TTCAGGGTAACATGA | 55213 |
rs762764086 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551443 | TCATCTGTTAGTGCT[A/G]GAGTATGTGCGTAAC | 55213 |
rs762764337 | snp | A/G | 1.65825e-05 | 0.00287941 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534267 | TCTTCTAAATCCTGG[A/G]CACACAACAAAAATA | 55213 |
rs762764935 | snp | C/G | 1.65345e-05 | 0.00287524 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541703 | CTGGCGGCAGGTCGA[C/G]TGTGTCTGTGTAGAG | 55213 |
rs762772008 | snp | C/T | 1.65353e-05 | 0.00287531 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541801 | TCATTCCAATACGAC[C/T]GGAACATGGATCGAA | 55213 |
rs762983971 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562405 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGCCCAGGA | 55213 |
rs763126943 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561272 | CACAGCAGTCCCCAG[A/G]CAACCAGGGGAAACA | 55213 |
rs763176002 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552458 | AAGGGGATGACAGAA[C/T]TGGCATCAGTTTCTA | 55213 |
rs763181683 | snp | C/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581890 | TTCACTGAGGTTGTG[C/G]GTGGAAGAGGCCAGG | 55213 |
rs763200325 | snp | A/G | 3.30633e-05 | 0.00406578 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549487 | CGCCACGAGACGGCG[A/G]GAGTGGCAAAGCAGG | 55213 |
rs763217480 | snp | G/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546995 | TCTGAAAAGAATGCC[G/T]GTGCCATTTTAAGAT | 55213 |
rs763236203 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569874 | GATCACAACGCTGCA[C/T]TCTAACCTGGGTGAC | 55213 |
rs763303546 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539376 | GTAAAGGAAATGACC[C/T]GCTGGCACAGGAAGC | 55213 |
rs763356320 | snp | C/G | 1.66062e-05 | 0.00288146 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540847 | AGGGAGTTAAAGGTG[C/G]TCTGGTTTCTGTTTG | 55213 |
rs763452239 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559985 | ACCACTTGCTTGATC[A/G]AGAGATTGGTACAGA | 55213 |
rs763455949 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555226 | TTCTTTAATCTATTA[C/T]ATTAAATATCACGAA | 55213 |
rs763456422 | in-del | -/TTTGGTTACA | 5.00221e-05 | 0.00500085 | intron-variant, splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49567324 | AGCCGACATCTCTGC[-/TTTGGTTACA]TGGAACAGAAAGGAT | 55213 |
rs763498663 | snp | A/T | 1.67144e-05 | 0.00289084 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559887 | TATGATGAAAAAAAA[A/T]AAGAATAAAGAATAA | 55213 |
rs763534188 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581406 | TTGAGTGAGAGAGAA[C/T]TGTGCTGCCACTCAC | 55213 |
rs763594801 | in-del | -/AAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551900 | GGGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 55213 |
rs763702629 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580476 | GTAGTTAGTCCCAGC[-/T]ACTCAAGAGGCTGAG | 55213 |
rs763727500 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569857 | GGCTGCAGTTGAGCC[A/G]AGATCACAACGCTGC | 55213 |
rs763769082 | snp | C/G | 3.32309e-05 | 0.00407607 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534272 | TAAATCCTGGACACA[C/G]AACAAAAATAAAAAC | 55213 |
rs763782679 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586615 | TTGACTACTCAACTT[C/T]CTTTGGATTATTTAC | 55213 |
rs763800812 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556290 | CCAGCCCCGCCTCCC[A/G]GGTTCATGTCATTCT | 55213 |
rs763840738 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573366 | CGTTTGTTTGTTTTC[A/G]TCAGCAGGGTTGTGG | 55213 |
rs763865636 | snp | C/T | 3.32044e-05 | 0.00407444 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540849 | GGAGTTAAAGGTGGT[C/T]TGGTTTCTGTTTGTT | 55213 |
rs764016499 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539268 | AGCTCCATGCCCACA[C/T]TGTGACAGACTCTGG | 55213 |
rs764024050 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581376 | AGAGCCGAAGATCAC[A/G]GGCAGACGCTGAGCT | 55213 |
rs764040985 | snp | C/G | 3.2956e-05 | 0.00405918 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566656 | GGTCCACTCCCGTAA[C/G]TGAGGCTTTTAATCT | 55213 |
rs764173443 | snp | A/G | 1.6563e-05 | 0.00287771 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567187 | GTACAGTGCTTCACT[A/G]GCTGAGGTGCCGAAG | 55213 |
rs764245180 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548848 | GCTTTCTTCTGGGGT[A/G]ATTAAAACAATTTAG | 55213 |
rs764447570 | snp | A/T | 3.31345e-05 | 0.00407016 | splice-acceptor-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544865 | AAAGTCTTCATGCTC[A/T]GAAGGCAACAAACAT | 55213 |
rs764505289 | snp | A/G | 4.98053e-05 | 0.00499001 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559905 | GAATAAAGAATAAAA[A/G]CAGCATACTTACCTC | 55213 |
rs764538827 | in-del | -/T | 1.79142e-05 | 0.00299279 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549413 | AAACTGGTCAGTTGG[-/T]TAGTACCATTCTTCC | 55213 |
rs764539493 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567832 | TAAACGCCGTCAAAT[C/G]AGGCTATTCATTGTC | 55213 |
rs764639189 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566929 | TCTGTGGACATTGCT[G/T]ACGTTTCAGAATGTT | 55213 |
rs764683766 | in-del | -/G | | | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567224 | GCCTTCCGAATAGAC[-/G]CGATCTCTTGAGGGG | 55213 |
rs764689195 | snp | A/G | 1.70702e-05 | 0.00292144 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549464 | CTTTCTTACCCACAG[A/G]CAGGAGGCGCCACGA | 55213 |
rs764707994 | in-del | -/GGGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568650 | AAATAATCAGGCCGG[-/GGGA]GGGAGGGGGGTGGCT | 55213 |
rs764784403 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541399 | TATGTAACAAGCCTA[C/T]ACATCCTGCACGTGT | 55213 |
rs764785957 | snp | C/T | 1.67005e-05 | 0.00288963 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534084 | ACATCCTCAACAGTG[C/T]CCCAGAGCACTCACA | 55213 |
rs764816390 | snp | A/G | 1.65993e-05 | 0.00288086 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560098 | ATCTGTGCACACAAA[A/G]CACACAAAAAATCAG | 55213 |
rs764897315 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575740 | CTGGAGACTACTACA[C/G]GGGCAGGGAGGGAGG | 55213 |
rs764906412 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566642 | TGAGAAGAACATGTG[A/G]TCCACTCCCGTAACT | 55213 |
rs764906670 | snp | C/T | 4.63682e-05 | 0.00481476 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552216 | AAGCTGCCACTCTCA[C/T]AGGGGTCAGCTGGTT | 55213 |
rs764918681 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567892 | TTGGATGTCTTGACA[A/C]ATGTGTGTGCAGGTG | 55213 |
rs764925896 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546870 | GTTAATAACAGGCCA[C/G]GGACCAGTACAGGCA | 55213 |
rs764939179 | in-del | CCCCTGCCCAA/GAGACCCTGTCTC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569706 | TGGGTGGCAGAGTGA[CCCCTGCCCAA/GAGACCCTGTCTC]AAAAAAAAAAAAGAA | 55213 |
rs765010474 | snp | C/T | 1.68653e-05 | 0.00290385 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551288 | GCCCCAAGGCCACAT[C/T]GCACACACAGTCCCA | 55213 |
rs765010861 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551901 | GGAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 55213 |
rs765072238 | snp | C/T | 1.85517e-05 | 0.00304557 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541040 | AAAGGTTTAATCAAA[C/T]GTATAATAATTTCCA | 55213 |
rs765084871 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553432 | GTGATAGGGGGATCA[A/T]GAGAGGGAAAGCAGA | 55213 |
rs765088709 | snp | C/T | 1.67265e-05 | 0.00289188 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541682 | CCACAGTACCTATAG[C/T]ATCTTCTGGCGGCAG | 55213 |
rs765224546 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583037 | AAAAAATTAGTCGAA[C/T]GTGGTGGTGCGCACC | 55213 |
rs765307655 | snp | A/G | 0.000142157 | 0.00842959 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549432 | TACCATTCTTCCTGG[A/G]TGGAGGTGGCCCTGC | 55213 |
rs765318943 | snp | A/G | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540654 | CTAGGACCTTGGTTC[A/G]TTTCCTGTCTTACTT | 55213 |
rs765367820 | in-del | -/AT | 1.64871e-05 | 0.00287111 | frameshift-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541737 | CTGGAGAAAGGCACG[-/AT]ACACTGGGTAAGAAA | 55213 |
rs765377368 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560246 | TAAAGGAGAGAGAGA[A/T]GGGTGACAGAACGGG | 55213 |
rs765377479 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579241 | CAGGCAAAGTTTCGA[A/G]GATGTGCTGAGACAC | 55213 |
rs765444780 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562040 | CCCAGGAGGCGGAGG[G/T]TGCAGTGGGCTGAGA | 55213 |
rs765463785 | snp | A/C | 1.65485e-05 | 0.00287645 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544855 | CAACTGTTAAAAAGT[A/C]TTCATGCTCTGAAGG | 55213 |
rs765487889 | snp | C/G | 0.000470588 | 0.0153321 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551296 | GCCACATCGCACACA[C/G]AGTCCCAAGACGTGG | 55213 |
rs765494092 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537617 | TGGTTAAACAAATAA[C/T]ACTTCCCAGCTGTTT | 55213 |
rs765572607 | snp | C/T | 6.61179e-05 | 0.00574931 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534261 | CAGAATTCTTCTAAA[C/T]CCTGGACACACAACA | 55213 |
rs765611914 | snp | C/T | 1.65288e-05 | 0.00287474 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555593 | AATATGTAAACAGTT[C/T]GTAACTTTTCGAGGA | 55213 |
rs765688931 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580823 | ACTGGCAGAACCATA[C/T]ACTATTAATTCAATA | 55213 |
rs765739804 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553599 | AGGAAAAAGTACTGA[C/T]CAGGAACAAATAAAG | 55213 |
rs765743400 | snp | C/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586824 | TGAGGTCTCGCTCCT[C/G]TTGCACTAGTTCCTG | 55213 |
rs765765470 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534983 | AGGTTGCGGTGAGCC[A/G]AGATCGCACCACTGC | 55213 |
rs765796462 | in-del | -/TGTGTGCTGGGCTT | 1.70313e-05 | 0.00291811 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549652 | TCTCTACCACCCTGA[-/TGTGTGCTGGGCTT]AAAGTTTTAAGAAAA | 55213 |
rs765825334 | in-del | -/CACT | | | intron-variant, splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49550463 | ATAATCAGAAGTCAG[-/CACT]CCAGGACATAGGAGG | 55213 |
rs765873381 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560013 | AGACCTGGACGGGAG[C/T]AATGCCTTGGTTGGT | 55213 |
rs765917521 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557369 | AAAGGAAATGGAGAG[A/G]AAATGGAGATGGTAC | 55213 |
rs766000378 | snp | C/T | 1.65053e-05 | 0.0028727 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560070 | CATTGTGGCCCCAGG[C/T]ATAAACCACTCCATC | 55213 |
rs766134054 | snp | A/T | 1.6898e-05 | 0.00290667 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567115 | AGACCAATTGCCAAA[A/T]AAGTCCTAAAACGAA | 55213 |
rs766202568 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571287 | GGAGGTGGAGGTTGC[A/G]GTGAACCGAGATTGC | 55213 |
rs766220671 | snp | A/G | 1.65277e-05 | 0.00287464 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551474 | CGCAGACAATCTGCA[A/G]GTAAATTGAAACGGT | 55213 |
rs766226482 | snp | C/T | 6.63416e-05 | 0.00575903 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567171 | CATCATTGTCAGTAA[C/T]GTACAGTGCTTCACT | 55213 |
rs766245043 | snp | A/G | 6.18257e-05 | 0.00555959 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552193 | CTGGTTCACACACAC[A/G]CTGTGCAAAGCTGCC | 55213 |
rs766281507 | snp | A/T | 1.65124e-05 | 0.00287331 | splice-donor-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540874 | TTTGTTGTTTAAGTT[A/T]CCTCTGCATCATATC | 55213 |
rs766309018 | in-del | -/AC | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549112 | ACTCCAGCCTGGGCG[-/AC]AGAGTGAGATTCTGT | 55213 |
rs766367437 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571874 | ACTGTTAAGAAAACC[A/G]CATTAAGGATCATAA | 55213 |
rs766412912 | in-del | -/GGTTCACACACACGCTGTGCAAA | 1.65173e-05 | 0.00287374 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49551470 | AACCGCAGACAATCT[-/GGTTCACACACACGCTGTGCAAA]GCAAGTAAATTGAAA | 55213 |
rs766414174 | snp | C/T | 3.29739e-05 | 0.00406028 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551453 | GTGCTAGAGTATGTG[C/T]GTAACCGCAGACAAT | 55213 |
rs766458868 | snp | C/T | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531708 | GAAACTCTGTATCCA[C/T]TAAACAAGTTCCCCA | 55213 |
rs766461767 | in-del | -/GTCAA | 1.68404e-05 | 0.00290171 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566573 | GCTTAGAATTAACCG[-/GTCAA]TTTCTTACAAACTGA | 55213 |
rs766491306 | snp | C/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581096 | AACTCAGGCTTTATC[C/G]TAAGAGCACCAGGTA | 55213 |
rs766495316 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552512 | GTCTGGGGCAAGTCA[C/G]TCTTTCCTGTTTAAT | 55213 |
rs766534517 | snp | C/G | 0.000446409 | 0.0149334 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552306 | AGAGGACAGAAGGGA[C/G]AGAGTGAGATTTTTA | 55213 |
rs766544968 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579452 | CACAGCGAAACCCCG[A/T]CTCTACTAAAAATAC | 55213 |
rs766548741 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539399 | CAGGAAGCAGCAGCA[C/G]AGGCTTTTTCTGTAA | 55213 |
rs766565371 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582243 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 55213 |
rs766625024 | snp | A/G | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555567 | CCACAGGCAATGCCA[A/G]CTACCCTCTTAATAT | 55213 |
rs766643600 | snp | A/C | 1.69198e-05 | 0.00290854 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541849 | CAGCAAAGCAAAAGT[A/C]TTATTTGTTCAGCAG | 55213 |
rs766750998 | snp | C/T | 1.66651e-05 | 0.00288657 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567318 | ATAAATAAGCCGACA[C/T]CTCTGCTGGAACAGA | 55213 |
rs766788687 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556605 | CTAAGCCCCCGCTCC[C/T]CACCCTGCTTCACGT | 55213 |
rs766805625 | snp | C/G | 6.65048e-05 | 0.00576611 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534102 | CAGAGCACTCACACA[C/G]AACCCAGCAGCCTTG | 55213 |
rs766873326 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574859 | CCATGAACAGATGAA[C/T]GGATAAACAAAATGT | 55213 |
rs766892734 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551622 | AAAGCATTAGAAGGC[C/T]GGGCGTGGTGGCTCA | 55213 |
rs766986050 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557316 | CTTGACCAAAGGCAA[C/T]GGAAATGGAGAGGAA | 55213 |
rs767038965 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547041 | AGCCTTTTATAACAA[A/G]TCCAGGTTAAGTAGT | 55213 |
rs767062548 | in-del | -/CGTTTTATA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555886 | CACTTTATACATCTC[-/CGTTTTATA]CATGGAAACTGAAAC | 55213 |
rs767098589 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537301 | AATATTCCAAATCAA[A/G]GAAGTTTTGTTTTGT | 55213 |
rs767150882 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554498 | CTCTAAAGCACCCTA[A/G]CACAGGGGTCCCCAG | 55213 |
rs767206025 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555131 | CAAGATATAGGTAGG[G/T]AGTTCTACAAGGACT | 55213 |
rs767227992 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533000 | CTTTTCAGGAACACC[A/G]TAATTTTGGTGCTTT | 55213 |
rs767388339 | snp | A/G | 1.80114e-05 | 0.00300089 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566814 | TTTTGACCGAAAGCT[A/G]TATTAAAAGCTCCCT | 55213 |
rs767434145 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551342 | TTTCTTTCTCCACCA[C/T]GATGTGTGCTGGGCT | 55213 |
rs767568936 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539471 | TCCAGCAACTTGAGC[C/T]GAGACATCTGCCTCT | 55213 |
rs767579796 | snp | A/T | 9.04282e-05 | 0.00672353 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552332 | TTTTAAACTGCTGGT[A/T]AGAAGGAAGAGACAA | 55213 |
rs767587030 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560530 | TATAGGGGAAAGAGA[C/T]AGACTGTTTACAAAG | 55213 |
rs767643485 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582028 | AATCACAGAATGTGA[C/T]AGAGTTGCAGGACGT | 55213 |
rs767667678 | snp | C/T | 1.65072e-05 | 0.00287286 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541712 | GGTCGACTGTGTCTG[C/T]GTAGAGGTACTGGAG | 55213 |
rs767681064 | snp | A/G | 1.65523e-05 | 0.00287678 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567202 | GGCTGAGGTGCCGAA[A/G]ACACACGCCTTCCGA | 55213 |
rs767690421 | in-del | -/C | 3.29516e-05 | 0.00405891 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566725 | GTACTCTGGTTATCT[-/C]CAGTTCCTAGACAGT | 55213 |
rs767749958 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570993 | TAAAGTCACTTCTTT[A/C]TGACTTTATCTTGCC | 55213 |
rs767753582 | snp | C/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585795 | CCGGTGGCTGCTGCC[C/G]GGACTTAGAGGCTTT | 55213 |
rs767774906 | snp | A/C | 1.66586e-05 | 0.00288601 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567305 | TCAAGCAATTCCTAT[A/C]AATAAGCCGACATCT | 55213 |
rs767816377 | snp | A/C | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555541 | CCAGAACAGCCATGG[A/C]TGAAGTCTGACCACA | 55213 |
rs767831872 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560048 | CCATTCCCAAGCTGG[C/T]TATATCCATTGTGGC | 55213 |
rs767855792 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558421 | AAGTAGGCTTGTCAT[A/G]GTGGCTATGCCTGTA | 55213 |
rs767930306 | snp | C/T | 1.69401e-05 | 0.00291029 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549472 | CCCACAGACAGGAGG[C/T]GCCACGAGACGGCGG | 55213 |
rs767940265 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577618 | AGCTAAGGAAAAGAG[C/T]GGGAAAAGAGTAAGC | 55213 |
rs767990406 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587562 | AAACCAGGGACCACA[A/G]ATCAGGGAGTCAGGG | 55213 |
rs768036752 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562822 | AAGAGACATGGCCTC[A/G]CTATGTTGACCAGGC | 55213 |
rs768049934 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576263 | GTGATGATTGTACAA[C/T]AATGTGAATGTACAT | 55213 |
rs768054001 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548825 | GTGTGACTAATTAAC[A/G]TATAAGGGCTTTCTT | 55213 |
rs768103071 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563637 | GCACTCCAGCCTAGG[A/C]GATAGAGCGAGACTG | 55213 |
rs768127883 | snp | C/T | 1.66402e-05 | 0.00288441 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567148 | TAGGTTTCAAGAGAC[C/T]CTTACCTCATCATTG | 55213 |
rs768196905 | in-del | -/T | 5.10083e-05 | 0.0050499 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566783 | CTAGAAAATAGATAG[-/T]TTTTTTTTCTGAGTC | 55213 |
rs768219209 | snp | C/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581625 | AAGGAGAGCAGAGTA[C/G]CTTAAGAAGAACTCT | 55213 |
rs768404310 | in-del | -/AGGAAATGGAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557356 | GGAACAAAAAGGCAA[-/AGGAAATGGAG]AGGAAATGGAGATGG | 55213 |
rs768453718 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534608 | CATTGTTGTAAAAGG[C/G]AGAATGCCACTTTAG | 55213 |
rs768460869 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558085 | AAAAATGTCAATTCC[C/T]GGCCAGGGCCACTGT | 55213 |
rs768475581 | snp | A/G | 1.65397e-05 | 0.00287569 | stop-gained, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544786 | ATTTTCCATCAATTC[A/G]AAACTTCAGATCAGC | 55213 |
rs768499869 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576983 | TCGTATTTTCTCTGG[A/C]ACTTGAAAATACATC | 55213 |
rs768606120 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575705 | GGTACACGTGGATAT[A/G]AAGACAGGAACAACA | 55213 |
rs768621323 | snp | A/G | 1.82537e-05 | 0.00302101 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555687 | ACCTACAAGAGAAAG[A/G]AAAAGGAAAAGGAAA | 55213 |
rs768635952 | in-del | -/AAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566288 | AATAAATAAATAAAT[-/AAA]TAAATAAATAAATAA | 55213 |
rs768648414 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535532 | ACTGCAGGTTTTGAC[C/T]GCACATTTCCAGCTA | 55213 |
rs768671822 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584126 | AAGTTCTTGCTGCAG[C/G]ATACGGGCACGCTTT | 55213 |
rs768726779 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571678 | GTGCCAGGCAGAACA[A/C]CAGAACAGGGTCCTT | 55213 |
rs768735589 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563289 | CCCAGGAGGTCAAGG[A/T]TGCAATGAGCCATAA | 55213 |
rs768765813 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550885 | GGTGGGTAGATCACT[C/T]GAGGCCAGGAGTTCA | 55213 |
rs768866667 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543482 | CTGTGGTTCAGATAT[A/T]TACTCCCTTAGGTAA | 55213 |
rs768909323 | in-del | -/AAAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562595 | CATAAAGGAGAAAAC[-/AAAG]AAGAAAATTTTTCTT | 55213 |
rs768920768 | snp | A/G | 1.6504e-05 | 0.00287258 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549553 | TGCGGGAGGATCACG[A/G]ACTGACCCCGGCACT | 55213 |
rs768941007 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572998 | GTACCCTGAGCAAGG[C/T]AGCCCAACTCTCTTC | 55213 |
rs769106452 | snp | C/T | 2.74262e-05 | 0.00370302 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552258 | CCAGGCCCAGCTGAC[C/T]GTTGCCATTGTAACC | 55213 |
rs769185495 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540964 | TGCTGACAAAGTTTT[C/T]TCAGTCTGTTTTCAC | 55213 |
rs769185609 | snp | C/G | 3.29522e-05 | 0.00405894 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560040 | TGGTCGTCCCATTCC[C/G]AAGCTGGCTATATCC | 55213 |
rs769191420 | snp | C/G/T | 3.29908e-05 | 0.00406132 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555573 | GCAATGCCAACTACC[C/G/T]TCTTAATATGTAAAC | 55213 |
rs769194260 | snp | A/G | 0.000118509 | 0.00769679 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552301 | CTTAGAGAGGACAGA[A/G]GGGAGAGAGTGAGAT | 55213 |
rs769433147 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543568 | TTTACCTAAATTTCC[-/A]AAAAGACTTGTAAAT | 55213 |
rs769434044 | snp | A/C/G | 3.29496e-05 | 0.00405881 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534193 | GGCCATCCATTTGCC[A/C/G]AAATGCTGCAGTCTG | 55213 |
rs769510106 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566728 | CTCTGGTTATCTCCA[A/G]TTCCTAGACAGTTAC | 55213 |
rs769518910 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577155 | TCTGAAAGCAAATTC[A/C]GTCAGGACAAACACA | 55213 |
rs769599340 | snp | C/T | 1.66468e-05 | 0.00288498 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567277 | CTTTCCGACATCCAC[C/T]ATGACTCTGGCTTCA | 55213 |
rs769600713 | snp | C/T | 1.72305e-05 | 0.00293513 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566789 | AAATAGATAGTTTTT[C/T]TTCTGAGTCTTTTGA | 55213 |
rs769635930 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536996 | AAAACAAAACACAGA[A/G]CATTGATGGTCTTAA | 55213 |
rs769671989 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567351 | GGATTCCAGAAAAAA[A/C]TTAAATAGTCACTGA | 55213 |
rs769721748 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578239 | ATCTCCAGATTACTT[A/G]TAATACCTAATACAA | 55213 |
rs769742101 | snp | A/C | 1.6519e-05 | 0.00287388 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541797 | GTCTTCATTCCAATA[A/C]GACTGGAACATGGAT | 55213 |
rs769794650 | snp | C/T | 1.70356e-05 | 0.00291848 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555651 | CCCACTTGGCCACAG[C/T]TGTTATAACCCCAAG | 55213 |
rs769937232 | snp | C/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587244 | TTGCCCAAAGTAGTG[C/G]CAGTTGAGTGAATTT | 55213 |
rs769994470 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533689 | CCAGGTCAGCATCTT[A/T]AATTCACGATGGGGC | 55213 |
rs770175569 | in-del | -/GCCACTTTCC | 1.66346e-05 | 0.00288393 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567258 | GTAGAGTGAAGATGG[-/GCCACTTTCC]GACATCCACCATGAC | 55213 |
rs770221068 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540951 | TCTCTTGATAATGTG[C/T]TGACAAAGTTTTTTC | 55213 |
rs770308810 | in-del | -/A | 0.000186306 | 0.00964979 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547115 | ATGCCATACATGTGC[-/A]ATTCTGGCCAAATAG | 55213 |
rs770325981 | snp | A/G | 3.32917e-05 | 0.0040798 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540844 | CAAAGGGAGTTAAAG[A/G]TGGTCTGGTTTCTGT | 55213 |
rs770351640 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540211 | CCTAATATGTGCCAG[A/G]CACTATAGGGTATAC | 55213 |
rs770390906 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578965 | GGTATACAACATTAC[A/G]ACTTAATGTCTTCCA | 55213 |
rs770424281 | snp | C/T | 8.70663e-05 | 0.00659739 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552151 | AGGTAGATGGGAAGC[C/T]ACTAACTGAGAGTGC | 55213 |
rs770474031 | snp | C/T | 1.65113e-05 | 0.00287322 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555517 | GGAGACACCTCACCT[C/T]GCCATTGTCCAGAAC | 55213 |
rs770497714 | in-del | -/CATCATATCTGACTGCAGCAGAGAATAGC | 1.65608e-05 | 0.00287752 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534265 | TTCTTCTAAATCCTG[lengthTooLong]GACACACAACAAAAA | 55213 |
rs770521995 | snp | C/T | 3.38318e-05 | 0.00411275 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541664 | TCGTCCATCCCAATG[C/T]TACCACAGTACCTAT | 55213 |
rs770524677 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548634 | CAGTCATAAAAGGGA[A/G]TGAAATACAGAGACA | 55213 |
rs770543389 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577398 | GAGAGAAATGGTACA[A/G]GAAAACTGGTTTTGA | 55213 |
rs770564028 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541781 | CTATCACTTCCTTCA[C/T]GTCTTCATTCCAATA | 55213 |
rs770683240 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548530 | GACAGCACTACCCAC[A/G]AGAGTCAAAGGTGGG | 55213 |
rs770755212 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575434 | ATAAATTGTTCTACC[-/AA]AAAAAAAAAAAAAAT | 55213 |
rs770771774 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537069 | TCTTACCCTGTCCTA[A/C]AACTCCAAAGCTAAA | 55213 |
rs770793185 | snp | A/G/T | 3.32664e-05 | 0.00407827 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567253 | GGAGAGTAGAGTGAA[A/G/T]ATGGGCCACTTTCCG | 55213 |
rs770802678 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538275 | CTAGAATACAGGCAT[A/G]AGCCACTGTGCCCAG | 55213 |
rs770878997 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576360 | CCAATTTTTTAAAAT[A/C]AAATAATCATCCTGT | 55213 |
rs771025454 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586233 | ACCTAAGAGGGCATC[C/T]GGTCCAACCGGATTC | 55213 |
rs771051679 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535267 | GAACCATTTCAAAAT[C/G]AATCCCTGCCTATGC | 55213 |
rs771068627 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561281 | CCCCAGGCAACCAGG[A/G]GAAACAGACTTCTAC | 55213 |
rs771070273 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575566 | TACACCATGGAATAC[C/T]ACATGGCCATAAAGA | 55213 |
rs771107673 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535486 | AAGGTCAGCACTCCG[G/T]GTTCTATCGAACCAG | 55213 |
rs771223356 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553280 | TATTAATTTAATTTG[C/T]ATTTTTGAAAGATAA | 55213 |
rs771228258 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582692 | TTACATGCCCACCGG[C/G]AATGTACAACAGTGC | 55213 |
rs771322328 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570239 | AATCATTAAACAAAT[-/A]ATGGGCAACTCTGCC | 55213 |
rs771339214 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570931 | TGGAGAATATCAGTC[C/T]TGGCCCTTGAAGGGC | 55213 |
rs771343098 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553433 | TGATAGGGGGATCAT[A/G]AGAGGGAAAGCAGAG | 55213 |
rs771363653 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551415 | GTTAGCTCCCCAGGC[A/G]TACAGCAAGCCCTCA | 55213 |
rs771384444 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566702 | CTTCTAGCTTTTTGG[A/G]TACAAGTGTACTCTG | 55213 |
rs771388444 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558358 | AACGGGTTGGAAAAT[G/T]AATGAATGAATAAAT | 55213 |
rs771402966 | snp | G/T | 1.7386e-05 | 0.00294834 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549675 | TAAGAAAAATGCATG[G/T]TACTTCATGATCACA | 55213 |
rs771451200 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534239 | ATGATTGATGCAAAA[C/T]TTAAAGCAGAATTCT | 55213 |
rs771494244 | in-del | -/G | 1.66704e-05 | 0.00288703 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567326 | GCCGACATCTCTGCT[-/G]GAACAGAAAGGATTC | 55213 |
rs771554373 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578656 | TAGGAAATAATTATG[A/T]GCAAACTAGTGACAA | 55213 |
rs771567237 | in-del | -/AAAAAAAAAAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562515 | GAGAGACCCTGTCTC[-/AAAAAAAAAAA]AAAAAAAAAATTTGG | 55213 |
rs771621125 | snp | C/T | 2.87733e-05 | 0.00379286 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552273 | CGTTGCCATTGTAAC[C/T]CCAGCCATATACCTT | 55213 |
rs771622704 | snp | A/G | 1.66255e-05 | 0.00288314 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567239 | GCGATCTCTTGAGGG[A/G]AGAGTAGAGTGAAGA | 55213 |
rs771634784 | in-del | -/CA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569728 | GTCTCAAAAAAAAAA[-/CA]AAGAAAGAAAGAAAG | 55213 |
rs771664503 | snp | C/G | 7.04548e-05 | 0.00593485 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552180 | GCACCACACGTACCT[C/G]GTTCACACACACGCT | 55213 |
rs771696161 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575869 | TGTAACAAACCTGCA[C/T]ATGTACTCCCTGAAT | 55213 |
rs771714672 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578501 | CAATCATGGTCTCTG[C/T]CTCTGAGGAACTGAA | 55213 |
rs771742758 | in-del | -/GCTGCC | 1.79175e-05 | 0.00299306 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555678 | AAGCAAACACCTACA[-/GCTGCC]AGAGAAAGAAAAAGG | 55213 |
rs771851382 | in-del | -/CAT | 0.000725665 | 0.0190343 | cds-indel, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540881 | TTTAAGTTACCTCTG[-/CAT]CATATCTGACTGCAG | 55213 |
rs771984712 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557040 | ATCTGGGGCATGAGG[C/G]CTGTGTGCTATGCCT | 55213 |
rs771986405 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544979 | CTTGTTTTTTTTTCA[A/G]GAGTTCATACCTTGT | 55213 |
rs772018414 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587592 | GAGAAACTTCATGAG[A/G]AGGTCAGTTGGACAG | 55213 |
rs772037802 | snp | C/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546704 | CCCTCGCATGTGCAG[C/T]TCACAATAGGGCTTA | 55213 |
rs772129159 | snp | C/G | 0.000116781 | 0.00764046 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549484 | AGGCGCCACGAGACG[C/G]CGGGAGTGGCAAAGC | 55213 |
rs772180688 | snp | C/T | 1.69436e-05 | 0.00291058 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549647 | CTGCAATCTCTACCA[C/T]CCTGAAAAGTTTTAA | 55213 |
rs772210757 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564424 | ACCCAGTCTCTACTA[A/T]AAGTACAAAAATTAG | 55213 |
rs772219799 | in-del | -/TG | 1.64754e-05 | 0.00287009 | frameshift-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534207 | CAAAATGCTGCAGTC[-/TG]TGTAACTTCTGTCAA | 55213 |
rs772268601 | snp | A/G | 0.000214205 | 0.0103468 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534224 | TGTAACTTCTGTCAA[A/G]TGATTGATGCAAAAC | 55213 |
rs772362926 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571535 | CAAGGTGCATCCTTG[A/G]GCTGGAGACTGCTAA | 55213 |
rs772412213 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554145 | GAATAGCAGAGAAAA[C/G]CTGCAGTAGGTATAA | 55213 |
rs772437131 | in-del | -/AGAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563344 | GTGACAGAGAGAGAG[-/AGAC]CCTGCCTCAAAAAAA | 55213 |
rs772480683 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566687 | TCTTTCCACATAAGC[C/T]TTCTAGCTTTTTGGG | 55213 |
rs772562283 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572748 | GGCAGAGGTTGCAGT[A/G]AGCCAAGACTATGCA | 55213 |
rs772585122 | snp | C/G | 1.65326e-05 | 0.00287507 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552184 | CACACGTACCTGGTT[C/G]ACACACACGCTGTGC | 55213 |
rs772592456 | snp | A/C | 1.65105e-05 | 0.00287315 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549573 | ACCCCGGCACTGGCC[A/C]CACATGTACACGTGC | 55213 |
rs772601559 | snp | C/T | 1.68032e-05 | 0.0028985 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540997 | TAAGATGTCGCCAAA[C/T]CCAGAAGACCTAAAA | 55213 |
rs772662592 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546874 | ATAACAGGCCACGGA[A/C]CAGTACAGGCATATG | 55213 |
rs772719408 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575870 | GTAACAAACCTGCAT[A/T]TGTACTCCCTGAATC | 55213 |
rs772721380 | snp | C/T | 6.01594e-05 | 0.00548417 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552281 | TTGTAACCCCAGCCA[C/T]ATACCTTAGAGAGGA | 55213 |
rs772782662 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575742 | GGAGACTACTACAGG[G/T]GCAGGGAGGGAGGGG | 55213 |
rs772859274 | in-del | -/TCTT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538807 | AAATAAAGAGGTGAG[-/TCTT]TCTTTTTGTCTTCTT | 55213 |
rs772879551 | in-del | -/AAGAT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552838 | TAGAAGCTAGTTTAG[-/AAGAT]AAGATAAGTAGGTGG | 55213 |
rs772921266 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558345 | CTGAACTGGAACAAA[C/T]GGGTTGGAAAATGAA | 55213 |
rs772948654 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535823 | AGGTCAGGAGTTTGA[A/G]ACCAGCTTGACCAAC | 55213 |
rs772972601 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548500 | CTACCCAAAAACTTA[C/T]ACAAGAACAGTCATG | 55213 |
rs772975755 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577314 | CTAATTTTATTTTAG[C/T]TTATTTTACTGATCT | 55213 |
rs773016795 | snp | C/T | 1.69502e-05 | 0.00291115 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567103 | TGGACACTTTGAAGA[C/T]CAATTGCCAAATAAG | 55213 |
rs773026330 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561974 | CAGGCATGGTAGCGC[A/G]CACCTGTAATCCCAG | 55213 |
rs773125807 | snp | A/C | 1.78761e-05 | 0.00298961 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549421 | TCAGTTGGTAGTACC[A/C]TTCTTCCTGGGTGGA | 55213 |
rs773253784 | snp | A/C | 3.33489e-05 | 0.0040833 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534092 | AACAGTGCCCCAGAG[A/C]ACTCACACAGAACCC | 55213 |
rs773254168 | snp | G/T | 1.7067e-05 | 0.00292117 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549656 | CTACCACCCTGAAAA[G/T]TTTTAAGAAAAATGC | 55213 |
rs773284626 | snp | A/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534225 | GTAACTTCTGTCAAA[A/T]GATTGATGCAAAACT | 55213 |
rs773414538 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573129 | CACATCCCAAATTCA[A/G]AACAAAACCACAAAA | 55213 |
rs773516004 | in-del | -/AAT | 1.66586e-05 | 0.00288601 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567305 | CAAGCAATTCCTATA[-/AAT]AATAAGCCGACATCT | 55213 |
rs773607266 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570916 | CTCTAATTTTTCTTA[C/T]GGAGAATATCAGTCC | 55213 |
rs773612598 | snp | A/G | 3.29821e-05 | 0.00406078 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555545 | AACAGCCATGGATGA[A/G]GTCTGACCACAGGCA | 55213 |
rs773622026 | snp | C/T | 6.59381e-05 | 0.00574149 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560057 | AGCTGGCTATATCCA[C/T]TGTGGCCCCAGGCAT | 55213 |
rs773677438 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540256 | GTTCCTGCTCACGAG[A/G]AGCTTACAGTCTGAT | 55213 |
rs773729886 | snp | C/T | 1.77112e-05 | 0.00297578 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566806 | TCTGAGTCTTTTGAC[C/T]GAAAGCTGTATTAAA | 55213 |
rs773746934 | in-del | -/CTGAGAAGAACATGTGGTC | 4.97343e-05 | 0.00498645 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560089 | ACCACTCCATCTGTG[-/CTGAGAAGAACATGTGGTC]CACACAAAGCACACA | 55213 |
rs773786710 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577437 | TGTTCTCAATATTAA[A/C]CAACAGTGGAAATTT | 55213 |
rs773825631 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573615 | CATCACGCCCGGCTA[A/G]TTTTGCATTTTTTTA | 55213 |
rs773930335 | snp | C/T | 1.66388e-05 | 0.00288429 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567149 | AGGTTTCAAGAGACT[C/T]TTACCTCATCATTGT | 55213 |
rs773943553 | in-del | -/A | 1.65722e-05 | 0.00287851 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534267 | TCTTCTAAATCCTGG[-/A]CACACAACAAAAATA | 55213 |
rs774006380 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567698 | GGGCGCCTGCAGCTG[C/G]AGCATGCTTAGCCAA | 55213 |
rs774015502 | snp | A/G | 3.31307e-05 | 0.00406992 | splice-donor-variant | RCBTB1 | GRCh38.p7 | 13:49552176 | GAGTGCACCACACGT[A/G]CCTGGTTCACACACA | 55213 |
rs774059699 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535921 | CCAGCTACTCAGGAA[A/G]CTGAGGCAGGAGAAT | 55213 |
rs774107708 | snp | C/T | 0.000186237 | 0.009648 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547118 | CCATACATGTGCAAT[C/T]CTGGCCAAATAGTCC | 55213 |
rs774110662 | snp | C/T | 4.96463e-05 | 0.00498203 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540860 | TGGTCTGGTTTCTGT[C/T]TGTTGTTTAAGTTAC | 55213 |
rs774132384 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543884 | TAGAGACAGTGTCTC[A/G]CTATATTGCCTAGGC | 55213 |
rs774201533 | snp | A/C | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544794 | TCAATTCGAAACTTC[A/C]GATCAGCAGTTTCTG | 55213 |
rs774208401 | in-del | -/TTA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547950 | CACCACCACTCCTGG[-/TTA]TTATTTTTTGTAGAG | 55213 |
rs774249342 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555887 | ACTTTATACATCTCC[A/G]TTTTATACATGGAAA | 55213 |
rs774275111 | snp | A/C | 1.84742e-05 | 0.0030392 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555688 | CCTACAAGAGAAAGA[A/C]AAAGGAAAAGGAAAG | 55213 |
rs774280816 | in-del | -/AGCAG | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582166 | GGGCCTTAAGAAAGT[-/AGCAG]AGCAGGGAATGGGAT | 55213 |
rs774311865 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584452 | AGTTACATCCTCGAC[C/T]CTGAAAGCAGTTTAA | 55213 |
rs774384002 | snp | C/G | 0.000117025 | 0.00764844 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534073 | ACAAACTGGACACAT[C/G]CTCAACAGTGCCCCA | 55213 |
rs774404843 | snp | A/G | 1.6525e-05 | 0.00287441 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549490 | CACGAGACGGCGGGA[A/G]TGGCAAAGCAGGCAA | 55213 |
rs774421256 | snp | A/G | 3.30147e-05 | 0.00406279 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549563 | TCACGGACTGACCCC[A/G]GCACTGGCCCCACAT | 55213 |
rs774427963 | in-del | -/A | 0.218276 | 0.247979 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547176 | CACAATACTCACTGC[-/A]AAAAAAAAAAAATAC | 55213 |
rs774443102 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540385 | AACCCAGTGCAAAAA[C/T]AAAAGGAGTCCACAG | 55213 |
rs774484373 | snp | C/G | 1.66515e-05 | 0.00288539 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567284 | ACATCCACCATGACT[C/G]TGGCTTCAAGCAATT | 55213 |
rs774494134 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581922 | TGCAGCAGGTTGAGG[C/T]GTATGTGAAAGGTGA | 55213 |
rs774548197 | snp | A/G | 1.8751e-05 | 0.00306189 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555698 | AAAGAAAAAGGAAAA[A/G]GAAAGAATAGTCAGG | 55213 |
rs774686105 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582719 | GTGCTGCTTTCTCCA[C/G]TATTTACTGTCTTTT | 55213 |
rs774821519 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570942 | AGTCCTGGCCCTTGA[A/G]GGGCTGAACTTCCTC | 55213 |
rs774836893 | snp | A/G | 1.65952e-05 | 0.00288051 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540983 | GTCTGTTTTCACAGT[A/G]AGATGTCGCCAAATC | 55213 |
rs774837922 | snp | C/T | 1.70406e-05 | 0.0029189 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541857 | CAAAAGTCTTATTTG[C/T]TCAGCAGCAATTTTT | 55213 |
rs774842821 | snp | C/G | 4.96381e-05 | 0.00498162 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544780 | GAATATATTTTCCAT[C/G]AATTCGAAACTTCAG | 55213 |
rs774850970 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578702 | ATATAACAGAAAACA[A/G]TTACACGAAATCCCA | 55213 |
rs774870914 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558385 | AAATGAATACAAATT[A/G]TTAGAAAATAAAAAT | 55213 |
rs774882350 | snp | A/C | 1.64762e-05 | 0.00287016 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560041 | GGTCGTCCCATTCCC[A/C]AGCTGGCTATATCCA | 55213 |
rs774903916 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567793 | CTTCAGCCCCAGGTA[C/T]CATACCACAAATTCA | 55213 |
rs774916822 | in-del | -/AAAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544478 | CTGTCTCAAAGAAAC[-/AAAC]AAACAAACAAACAAA | 55213 |
rs774924631 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538634 | GGAAGGAGGACTACT[C/T]GAGCCCAGGAAGTTG | 55213 |
rs775088372 | in-del | -/G | 1.7339e-05 | 0.00294435 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559878 | TGTATTTACTATGAT[-/G]AAAAAAAAAAAGAAT | 55213 |
rs775112132 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580402 | CCAGCCTGGGCAACA[C/T]GGCGAGACTCCATTT | 55213 |
rs775140891 | snp | C/G | 4.8486e-05 | 0.00492348 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552310 | GACAGAAGGGAGAGA[C/G]TGAGATTTTTAAACT | 55213 |
rs775159781 | snp | C/G/T | 9.88882e-05 | 0.00703103 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566737 | TCTCCAGTTCCTAGA[C/G/T]AGTTACTATAGTTCA | 55213 |
rs775168953 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568714 | GGTGGGCAGATCAGG[A/C]GGTCAAGAGATCGAG | 55213 |
rs775200452 | snp | A/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587593 | AGAAACTTCATGAGA[A/T]GGTCAGTTGGACAGG | 55213 |
rs775240579 | in-del | -/TG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583389 | GTGCTTTTGTGTATG[-/TG]TGTGTGTGTGTGTGT | 55213 |
rs775243506 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559062 | AGAAATATACCATAG[A/G]AACTTAACTCTTGTT | 55213 |
rs775320050 | snp | C/T | 1.74467e-05 | 0.00295348 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566799 | TTTTTTTTCTGAGTC[C/T]TTTGACCGAAAGCTG | 55213 |
rs775355530 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586434 | TGTTCACTTACCTTT[C/T]CCATTTGAGCTCCTA | 55213 |
rs775372034 | snp | G/T | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555529 | CCTCGCCATTGTCCA[G/T]AACAGCCATGGATGA | 55213 |
rs775385614 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546792 | TAATGTGAGTGATGG[A/G]GAGCAGCTGTAAATA | 55213 |
rs775441887 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562384 | GTAATCCCAGCACTT[C/T]TGGAAGCTGAGGTGG | 55213 |
rs775505360 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584072 | GGAAAAGGAGGGTAC[G/T]GTTTCAGACTTCCCA | 55213 |
rs775567684 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582901 | TGGAGTGGAGGCCGG[C/G]TGTGGTTGCTCACGC | 55213 |
rs775631456 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559978 | TACTTCCACCACTTG[C/T]TTGATCAAGAGATTG | 55213 |
rs775650213 | snp | A/G | 1.77489e-05 | 0.00297895 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549434 | CCATTCTTCCTGGGT[A/G]GAGGTGGCCCTGCAC | 55213 |
rs775735936 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563661 | GAGACTGTCTCAAAA[-/G]AAAAAAAAGGAAAGA | 55213 |
rs775779841 | snp | C/T | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540485 | TACAAATCATACACA[C/T]CCCCAGCTTATGACA | 55213 |
rs775925323 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560194 | TTCATTTCTCTCCCA[C/T]TGCCCCCTCCTCTCT | 55213 |
rs775997538 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535882 | ACAAAAATTAGCCAG[A/G]TGTGGTGGCAAGCAC | 55213 |
rs776010231 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49531957 | TGTGCCTGTTTTAAT[C/G]TTACTTTGTTTATTA | 55213 |
rs776101316 | snp | C/T | 4.95013e-05 | 0.00497475 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555522 | CACCTCACCTCGCCA[C/T]TGTCCAGAACAGCCA | 55213 |
rs776103256 | snp | C/G | 1.68496e-05 | 0.0029025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541670 | ATCCCAATGCTACCA[C/G]AGTACCTATAGCATC | 55213 |
rs776121415 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541794 | CATGTCTTCATTCCA[A/G]TACGACTGGAACATG | 55213 |
rs776219215 | snp | A/C | 1.65723e-05 | 0.00287852 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567180 | CAGTAACGTACAGTG[A/C]TTCACTGGCTGAGGT | 55213 |
rs776338022 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575710 | ACGTGGATATAAAGA[C/G]AGGAACAACAGACAC | 55213 |
rs776458453 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548548 | AGTCAAAGGTGGGAA[C/T]AACCCACATGTCCAT | 55213 |
rs776470228 | snp | A/G | 8.26276e-05 | 0.00642705 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566625 | CTCCTTACCTTCGGT[A/G]CTGAGAAGAACATGT | 55213 |
rs776521542 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535621 | CTTTTCTGCTCTCAG[A/C]ACAGACCTCTGCAAA | 55213 |
rs776620487 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535512 | ACCAGAAGCTCAACA[C/T]TTCAACTGCAGGTTT | 55213 |
rs776747999 | snp | A/G | 6.66978e-05 | 0.00577446 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540834 | GAGACGAGCACAAAG[A/G]GAGTTAAAGGTGGTC | 55213 |
rs776757167 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559942 | AGCTGCCAGAGCCAT[C/T]GAATGATGTGAGCCA | 55213 |
rs776764482 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534505 | ACTCTTCAAAACACA[C/G]ACGCGCGCGCACACA | 55213 |
rs776800388 | in-del | -/G | 1.7814e-05 | 0.00298441 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549430 | AGTACCATTCTTCCT[-/G]GGTGGAGGTGGCCCT | 55213 |
rs776872087 | snp | C/T | 1.7419e-05 | 0.00295114 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549676 | AAGAAAAATGCATGT[C/T]ACTTCATGATCACAG | 55213 |
rs776907529 | snp | C/G | | | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531650 | GTCTGTGGCCCGAGG[C/G]TTGGGGACCCCTGAC | 55213 |
rs777015724 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533601 | AGCACACAAACAAAA[G/T]TCTGAAACAATCTTA | 55213 |
rs777032441 | snp | C/T | 1.65209e-05 | 0.00287405 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544829 | ATCAAATTCTTTCTT[C/T]AGTGACTCTGCAACT | 55213 |
rs777049151 | snp | C/T | 1.65274e-05 | 0.00287462 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549590 | ACATGTACACGTGCC[C/T]ACCCTGCGTCTTGGC | 55213 |
rs777096686 | snp | A/G | 4.16884e-05 | 0.00456535 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552303 | TAGAGAGGACAGAAG[A/G]GAGAGAGTGAGATTT | 55213 |
rs777153155 | snp | C/T | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551421 | TCCCCAGGCATACAG[C/T]AAGCCCTCATCTGTT | 55213 |
rs777269027 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572445 | AAAGTATTAACAGAC[C/T]TATTCTAACTATGGA | 55213 |
rs777364358 | snp | C/G | 1.65375e-05 | 0.0028755 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555500 | GAAAGGGAAATGGGA[C/G]TGGAGACACCTCACC | 55213 |
rs777383465 | in-del | -/AT | 3.31802e-05 | 0.00407296 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544879 | CTGAAGGCAACAAAC[-/AT]ATATTAATATGGCAA | 55213 |
rs777401686 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532004 | ATTACATAAATACAG[C/T]TTACATACTAGAGTA | 55213 |
rs777411573 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571385 | TCCCAATAAAAAGCA[C/T]TCCGCAAAATGCTTC | 55213 |
rs777450350 | in-del | -/TTTA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560583 | TTTGAAGCAGACTAT[-/TTTA]TTTTAGTGGCATGAA | 55213 |
rs777487842 | snp | C/G | 1.64942e-05 | 0.00287173 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534125 | CAGCCTTGCGCTTCA[C/G]TTCTTAAAGGCTCCA | 55213 |
rs777543313 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559242 | ATCCTATCATATGGT[A/G]CAAAGTGGATGAACC | 55213 |
rs777558991 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568409 | CTAAAATAAATTCCT[-/A]AAAAATGAAAATTGC | 55213 |
rs777588629 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578243 | CCAGATTACTTATAA[C/T]ACCTAATACAATGTA | 55213 |
rs777610386 | snp | A/C/T | 3.2948e-05 | 0.00405871 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560029 | AATGCCTTGGTTGGT[A/C/T]GTCCCATTCCCAAGC | 55213 |
rs777630688 | in-del | -/T | 0.000696524 | 0.0186488 | frameshift-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552182 | ACCACACGTACCTGG[-/T]TCACACACACGCTGT | 55213 |
rs777654859 | snp | G/T | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546541 | ACTGTAATATGTAAT[G/T]AAATAATTACACAAC | 55213 |
rs777699498 | snp | C/T | 3.36005e-05 | 0.00409867 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566777 | CAAAGACCTAGAAAA[C/T]AGATAGTTTTTTTTC | 55213 |
rs777713085 | snp | C/T | 6.66911e-05 | 0.00577418 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549485 | GGCGCCACGAGACGG[C/T]GGGAGTGGCAAAGCA | 55213 |
rs777722379 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567510 | CAAACCCCGGACTTT[A/C]CTACAAGAGAATAAC | 55213 |
rs777761319 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538024 | CAGGTAGTCTCCATC[C/T]TCCTAGCATTTTGGC | 55213 |
rs777802605 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549545 | GGGTGAGGTGCGGGA[A/G]GATCACGGACTGACC | 55213 |
rs777820369 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572676 | GGGTGTGGTGGCGCA[C/T]GCTGGTAATCTCAGC | 55213 |
rs777830241 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534512 | AAAACACACACGCGC[A/G]CGCACACACACACAC | 55213 |
rs777850446 | in-del | -/TGTGTA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583381 | AAAGAAGTGTGCTTT[-/TGTGTA]TGTGTGTGTGTGTGT | 55213 |
rs777976221 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541775 | CGATTTCTATCACTT[C/T]CTTCATGTCTTCATT | 55213 |
rs778026378 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547505 | AAATATGCTAGCAAA[A/T]AGGCAAACATAAACA | 55213 |
rs778058326 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563797 | GATTTGGATTTCACA[A/G]CTCTCTTGAGAAAGA | 55213 |
rs778082215 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581344 | TGGGACAAGGAGCAC[C/T]GGATAAGCAGAAAGG | 55213 |
rs778105429 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582662 | CTCATTCTCTCTCCC[C/T]GCTGAGTCTCCATTT | 55213 |
rs778147398 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576546 | CGGAGCATTTATAAA[A/G]GAAATATAGCCTTCT | 55213 |
rs778357364 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583517 | AACACTCATCATACC[A/C]CTCTTGTGCATTCTT | 55213 |
rs778369520 | snp | A/T | | | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544783 | TATATTTTCCATCAA[A/T]TCGAAACTTCAGATC | 55213 |
rs778394434 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536206 | GTTCCAAACATTAAA[A/G]GCCAAACTAGAGAAT | 55213 |
rs778406040 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560768 | GACTTGAGAGTTGAG[A/G]ACTAGCAACACCTGG | 55213 |
rs778444618 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579875 | AATTTTAGAGGAAAA[C/T]GTAAGTTCCTACAAC | 55213 |
rs778463542 | snp | C/T | 3.34622e-05 | 0.00409023 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549482 | GGAGGCGCCACGAGA[C/T]GGCGGGAGTGGCAAA | 55213 |
rs778629712 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565162 | TGCGATTGCAGGGGC[A/G]CGCCGCCACACCTGA | 55213 |
rs778646507 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49540893 | CTGCATCATATCTGA[C/T]TGCAGCAGAGAATAG | 55213 |
rs778686937 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550907 | AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGC | 55213 |
rs778771027 | in-del | -/AC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538756 | TATGAATATATATAT[-/AC]ATACACACACACACA | 55213 |
rs778814801 | in-del | -/G | 1.66899e-05 | 0.00288871 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534081 | GACACATCCTCAACA[-/G]TGCCCCAGAGCACTC | 55213 |
rs778835827 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581450 | ACAGCAGGCCTCAGG[A/G]GTGATGAGTCCTACT | 55213 |
rs778856666 | snp | G/T | 1.64887e-05 | 0.00287125 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559937 | CCATCAGCTGCCAGA[G/T]CCATTGAATGATGTG | 55213 |
rs778886612 | in-del | -/C | 0.000134798 | 0.00820859 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560132 | AAAAAGAAATAGTAA[-/C]CCCTGTACTTTCTTC | 55213 |
rs778969373 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566676 | GCTTTTAATCTTCTT[C/T]CCACATAAGCCTTCT | 55213 |
rs779059509 | snp | C/T | 1.67939e-05 | 0.0028977 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549638 | AGTGACAGGCTGCAA[C/T]CTCTACCACCCTGAA | 55213 |
rs779061467 | snp | C/T | 1.65548e-05 | 0.002877 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566762 | AGTTCAGTCCAAATA[C/T]AAAGACCTAGAAAAT | 55213 |
rs779104348 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536523 | AACAGGCAAGAAAAT[C/G]CAACTCCTGTCCAAG | 55213 |
rs779125320 | snp | A/G | 0.000389994 | 0.0139587 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552259 | CAGGCCCAGCTGACC[A/G]TTGCCATTGTAACCC | 55213 |
rs779171535 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576930 | AGGTAGAAAGAGTGT[A/G]ACGTCCTTAAAGATA | 55213 |
rs779228335 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564237 | AGATGAAGATTTCCC[C/G]ATTCAAGATGCAAGC | 55213 |
rs779240505 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571415 | CTGCCTAGATTTGCC[C/T]GGTTAAACCTCATGA | 55213 |
rs779258513 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543067 | CAGGAGTTTGAGACC[G/T]GCCTGGCCAACATGG | 55213 |
rs779316863 | snp | C/G | 1.6693e-05 | 0.00288898 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567330 | ACATCTCTGCTGGAA[C/G]AGAAAGGATTCCAGA | 55213 |
rs779357551 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574686 | GATGGTGATTCCTTA[-/AA]AAAAAAAAAAAACAT | 55213 |
rs779402696 | snp | C/T | 0.00011578 | 0.00760767 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555495 | AGGTAGAAAGGGAAA[C/T]GGGAGTGGAGACACC | 55213 |
rs779423093 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532081 | CTTAAGAAATATGAA[C/T]ACTTTGGCTTCCATT | 55213 |
rs779485815 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572673 | CCCGGGTGTGGTGGC[A/G]CACGCTGGTAATCTC | 55213 |
rs779488974 | snp | A/C/G | 0.000814982 | 0.0201702 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541651 | TCCACCATGCGGCTC[A/C/G]TCCATCCCAATGCTA | 55213 |
rs779501771 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544273 | TCGGGAGTTCGAGAC[C/T]AACCTGACCAACATG | 55213 |
rs779505354 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541742 | GAAAGGCACGATACA[C/T]TGGGTAAGAAAACTG | 55213 |
rs779516910 | snp | A/C/T | 3.36997e-05 | 0.00410474 | stop-gained, missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549474 | CACAGACAGGAGGCG[A/C/T]CACGAGACGGCGGGA | 55213 |
rs779593127 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562266 | GTTAAAAATTTGACA[A/T]AAGCGTTGTAAGATA | 55213 |
rs779598028 | snp | C/G | 1.65247e-05 | 0.00287438 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559918 | AAGCAGCATACTTAC[C/G]TCTCCATCAGCTGCC | 55213 |
rs779598329 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539819 | GACCTTATCAAATAT[C/T]TATAATCAGAATATA | 55213 |
rs779616383 | in-del | -/TGCTTCACTGGCTGAGGTGCCGAAGACAC | 1.6842e-05 | 0.00290184 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566779 | AGACCTAGAAAATAG[lengthTooLong]ATAGTTTTTTTTCTG | 55213 |
rs779675956 | snp | A/C/G/T | 0.00044925 | 0.0149815 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552174 | GAGAGTGCACCACAC[A/C/G/T]TACCTGGTTCACACA | 55213 |
rs779684426 | snp | C/G | 1.66299e-05 | 0.00288352 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544902 | ATATGGCAAGTTCAA[C/G]GAACAGATTGAAGAT | 55213 |
rs779765494 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585901 | GTCGGCCTACCACCC[C/T]AGAGACCTAGGACGG | 55213 |
rs779770604 | snp | A/G | 1.68038e-05 | 0.00289855 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534295 | ATAAAAACAAAAATG[A/G]CTTTTTTAGGCAACT | 55213 |
rs779795713 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551348 | TCTCCACCATGATGT[A/G]TGCTGGGCTTAGCAG | 55213 |
rs779812460 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581576 | AGATTTGGAAATCTG[A/G]CATGAAATCACCCAG | 55213 |
rs780002148 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547976 | TAGAGATGGGGTTTC[A/G]CCATGTTGCCCAGGC | 55213 |
rs780021535 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557999 | TGAATAGACAAACAA[A/C]GTGTGGCTTACAGCA | 55213 |
rs780159362 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578112 | GTATCTGTGGGGGAC[C/T]GGTTCCAGGATCTCC | 55213 |
rs780258659 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557086 | CAGTCATGAAATCTT[C/G]GTCTCCCTGAGCTTT | 55213 |
rs780311538 | in-del | -/CTGATTTT | 1.66946e-05 | 0.00288912 | frameshift-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544737 | CTCATGCAAAAATAC[-/CTGATTTT]CAAAACAGCTTTATG | 55213 |
rs780321910 | in-del | -/AG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538909 | TTTTTTTTTTGAGAC[-/AG]AGTCTTGCTCTGTTG | 55213 |
rs780322567 | snp | A/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586949 | TCCAGGTCAAATGCC[A/G]CCTACTCTTGTCTTC | 55213 |
rs780402049 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568799 | TGGGCATGGTGGTGT[-/A]GTGCCTGCAGTCCCA | 55213 |
rs780457030 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543314 | AAAAAATAGTTTCAC[C/T]TACATAAAAAATTAC | 55213 |
rs780491933 | in-del | -/AAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562515 | GAGAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 55213 |
rs780505945 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544361 | GTAATCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 55213 |
rs780573370 | snp | C/T | 1.65952e-05 | 0.00288051 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552173 | TGAGAGTGCACCACA[C/T]GTACCTGGTTCACAC | 55213 |
rs780658339 | snp | A/G | | | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534158 | TTTACTGGCTTTAGC[A/G]ATGAATTCCTTTAGC | 55213 |
rs780663197 | snp | A/C | 2.64309e-05 | 0.00363521 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552249 | CATTGTTTCCCAGGC[A/C]CAGCTGACCGTTGCC | 55213 |
rs780691181 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540048 | CATGCACAACTTAGC[C/T]AGATATTTTGAAACT | 55213 |
rs780700594 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541438 | ACTTAAAAATAAATT[A/T]AAAAAAAAAAAGTCC | 55213 |
rs780717050 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558135 | CATGTCTGTGTGGGT[A/T]TTCTCTGGGTACTCT | 55213 |
rs780755741 | in-del | -/ATT | 1.66065e-05 | 0.00288149 | cds-indel, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567160 | GACTCTTACCTCATC[-/ATT]GTCAGTAACGTACAG | 55213 |
rs780860790 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583244 | AGTCACCAGGGAGGA[C/T]GGGAAAGAGCACTGA | 55213 |
rs780919658 | snp | C/T | 1.66568e-05 | 0.00288585 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549625 | GACGTGTGGGCAGAG[C/T]GACAGGCTGCAATCT | 55213 |
rs780939449 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570763 | GCCTTGTCGTAGACA[C/T]TGTTAATTAGGTAGC | 55213 |
rs780945423 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583371 | CTACCCCAGGAAAGA[A/T]GTGTGCTTTTGTGTA | 55213 |
rs780946842 | snp | A/C | 6.59e-05 | 0.00573983 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566667 | GTAACTGAGGCTTTT[A/C]ATCTTCTTTCCACAT | 55213 |
rs780965666 | in-del | -/CT | 1.654e-05 | 0.00287571 | splice-acceptor-variant | RCBTB1 | GRCh38.p7 | 13:49534262 | GAATTCTTCTAAATC[-/CT]CTGGACACACAACAA | 55213 |
rs781003094 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578152 | TAAAATCCACAGATG[C/T]TCAAGTCCCTGATAG | 55213 |
rs781013421 | in-del | -/CAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553944 | AGTAACATAGAAAAT[-/CAC]CACAACTCTGTCTAT | 55213 |
rs781095610 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559179 | ATGTGGGCACTTACT[A/G]TATGTATCCAATGGA | 55213 |
rs781218769 | snp | A/T | 3.334e-05 | 0.00408276 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534281 | GACACACAACAAAAA[A/T]AAAAACAAAAATGGC | 55213 |
rs781308353 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569300 | AAATAAAGGCTGGGC[A/G]CAGTAGCTCACGCCT | 55213 |
rs781395937 | snp | C/T | 3.4706e-05 | 0.00416555 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552236 | GTCAGCTGGTTGCCA[C/T]TGTTTCCCAGGCCCA | 55213 |
rs781413981 | snp | C/G | 3.46182e-05 | 0.00416028 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541641 | GGATATATTCTCCAC[C/G]ATGCGGCTCGTCCAT | 55213 |
rs781493775 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573911 | GCCTCAGCCTCCCGA[A/G]TAGCTGGAATTACAG | 55213 |
rs781530140 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544411 | GAGGCAGAGGTTGCG[A/G]TGAGCTGAGATCGTG | 55213 |
rs781604758 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545013 | ACAAATCAATTCTAC[A/G]GTATTAAAGTAAGTA | 55213 |
rs781621849 | in-del | -/AAGCTTAACTC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547261 | GTTTCACTTTAAGGC[-/AAGCTTAACTC]TTCCTAAGCACCCTT | 55213 |
rs781700591 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566783 | CCTAGAAAATAGATA[G/T]TTTTTTTTCTGAGTC | 55213 |
rs796115391 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551975 | TTTTTTTTTTTTTTT[-/T]AACTTGTCGAGCCTG | 55213 |
rs796195932 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566265 | TGATCAATAAAAAAA[A/T]AAAATAAAATAAATA | 55213 |
rs796230496 | in-del | -/GCCCGGCCGCCCCGTCTGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565659 | GTGAGGAGCGTCTCT[-/GCCCGGCCGCCCCGTCTGA]GAAGTGAGGAGCCCC | 55213 |
rs796283520 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551962 | TGAATTTTTCCATTT[G/T]TTTTTTTTTTTTTAA | 55213 |
rs796290320 | in-del | AA/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569428 | AAATACAAAAAAAAA[AA/T]GCCAGGCACGGTAGC | 55213 |
rs796327801 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563660 | CGAGACTGTCTCAAA[-/A]GAAAAAAAAGGAAAG | 55213 |
rs796350003 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580165 | TGTTGTTTTCAAAAG[-/G]AAACCAGAAAAGAAA | 55213 |
rs796363511 | in-del | AAATAAATAAATAAATA/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566288 | ATAAATAAATAAATA[AAATAAATAAATAAATA/T]AAAAGTTGCATTGCA | 55213 |
rs796436521 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535049 | GAAAATCCCAAAAAA[A/T]TCACCTTAAATTCAC | 55213 |
rs796441613 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542228 | CAAAAAAAAAAAAAA[-/A]GTAAGTATATTAACT | 55213 |
rs796459436 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532177 | ACAAGTAGAAAAATA[-/AG]AGAGTGTATTTAAAA | 55213 |
rs796482665 | in-del | -/A | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586755 | TAAAAAAAAAAAAAA[-/A]GGTATTAAGAAACTA | 55213 |
rs796498631 | in-del | -/TGTGTG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583387 | GTGTGCTTTTGTGTA[-/TGTGTG]TGTGTGTGTGTGTGT | 55213 |
rs796543388 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560504 | GGGCGTGTGGCTACT[C/G]GCTCACCAAGTATAG | 55213 |
rs796575516 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584690 | GGGCAAAAGCAAGGA[A/C]GATCATGAATCTGGT | 55213 |
rs796582177 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585221 | TCCTTCCCTCCTCCT[C/T]GCAGGAGAGCACATT | 55213 |
rs796600051 | in-del | AGC/GG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562774 | GTGCCACCATCCCCG[AGC/GG]TTTTTTTTTTTTTTT | 55213 |
rs796611339 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560627 | ATTTTTTTTTTTTTT[-/T]ACATAAAGCAACCAT | 55213 |
rs796637216 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562230 | TCAAGAAAGAACACT[C/T]GGAAATAAAACAATG | 55213 |
rs796643525 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534831 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 55213 |
rs796644384 | in-del | G/TT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551961 | TGAATTTTTCCATTT[G/TT]TTTTTTTTTTTTAAC | 55213 |
rs796676755 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561203 | GTCTGCCTGGCAACA[A/C]CACTCAAGGGCAACA | 55213 |
rs796757395 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536200 | TCAAAAGTTCCAAAC[A/C]TTAAAAGCCAAACTA | 55213 |
rs796785615 | in-del | AGT/GG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542228 | AAAAAAAAAAAAAAA[AGT/GG]AGTATATTAACTACT | 55213 |
rs796805492 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559673 | AAAAAAAAAAAAAAA[A/G]AAAGTTGTTGTCAGG | 55213 |
rs796822241 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561944 | TAAAAAAAAAAAAAA[-/AA]TACAAAAATCAGCCA | 55213 |
rs796834496 | in-del | AA/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564897 | TCCGTCTCAAAAAAA[AA/G]AAGAAAGAAAGAAAA | 55213 |
rs796837597 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574888 | GTGGTCTACACATAC[A/G]ATAGAATATTATTCA | 55213 |
rs796864626 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556364 | CCCGGCTAATTTTTT[G/T]TATTTTTAGTAGAGA | 55213 |
rs796874148 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564377 | GGATCACGAGGTCAG[C/G]AGTTCCAGACCAACC | 55213 |
rs796886396 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559879 | GTATTTACTATGATG[-/AA]AAAAAAAAAGAATAA | 55213 |
rs796998814 | snp | A/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586741 | CCAGGGCCAATGATT[A/T]AAAAAAAAAAAAAAG | 55213 |