SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8596 | snp | A/G | 0.34526 | 0.23114 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416582 | CATGAACGTTTTAAC[A/G]TAGTAAATCCTCTTT | 8208 |
rs9108 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376454 | CGTGTCGGTCATATA[C/T]AGTATTGAATTTTTA | 8208 |
rs170144 | snp | A/G | 0.498754 | 0.0249289 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407192 | gcctcaggctcttga[A/G]tagctgggattacag | 8208 |
rs190068 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410628 | gaggcacagaatata[C/T]aaggaaaacccaaag | 8208 |
rs218623 | snp | C/T | 0.250168 | 0.25 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378958 | GAAAATTAAAATGGC[C/T]AATGTAAGGACTGAG | 8208 |
rs218624 | snp | C/T | 0.250168 | 0.25 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379076 | GTGTCTGGGTAGTTT[C/T]TGGGTGGTGTGTGGC | 8208 |
rs218625 | snp | C/T | 0.250168 | 0.25 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381472 | AAAGAGACTATATTA[C/T]AGTCTCTTTTAGTTC | 8208 |
rs218626 | snp | C/T | 0.434398 | 0.168811 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381734 | tatcatattgggctc[C/T]gattttctggagaac | 8208 |
rs218627 | snp | A/G | 0.493793 | 0.055364 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383737 | GGCGTGAACCCGGGA[A/G]GCGGGGCTTGCAGTG | 8208 |
rs218628 | snp | C/T | 0.29278 | 0.246313 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391054 | AACAGCAAAGAACCC[C/T]CAGTGCAAGGGTTGG | 8208 |
rs218629 | snp | G/T | 0.322959 | 0.239117 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410045 | acctgggaggcaggg[G/T]ttgcagtgagccaag | 8208 |
rs218630 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411772 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGTGAT | 8208 |
rs218631 | snp | A/G | 0.427575 | 0.175975 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413706 | CACCAAGAGGAAGAG[A/G]TGTCCAGGGCTTCCC | 8208 |
rs218646 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402090 | AAAACAACATTTCTT[C/T]AACACCTGTCTGGGA | 8208 |
rs218647 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403359 | AGCGATTCTCCTGCC[G/T]CAGTCTCCCAAGTGG | 8208 |
rs218648 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404653 | tgaggtccggagttc[A/G]agaccagactgacca | 8208 |
rs218649 | snp | A/G | 0.49089 | 0.0668743 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406388 | tgaggcagaagaatc[A/G]cttgaactcaggaga | 8208 |
rs218650 | snp | G/T | 0.493107 | 0.0583 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406532 | ttgggaggctgaggc[G/T]ggtggatcacctgag | 8208 |
rs218651 | snp | A/G | 0.481009 | 0.0955756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407850 | GCCGGGATTACAGGC[A/G]CCTGCCACGATGCCC | 8208 |
rs218652 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408524 | GTGGGCAATCCCCGG[A/G]GACCTGGTTCTGATC | 8208 |
rs968599 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383462 | TCTTAACTCAGCTTC[A/G]AAAAAAAACTTCTCA | 8208 |
rs1063308 | snp | A/G | 0.0514469 | 0.15191 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375309 | TAAAGTATATGTTAT[A/G]TAAGATAAAATATTT | 8208 |
rs1906483 | snp | A/G | 0.495056 | 0.049474 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396833 | ATGACAAAGAGGGTC[A/G]CTAGTTAGGAGGTGA | 8208 |
rs1906484 | snp | C/G | 0.141258 | 0.225111 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396825 | GAGGGTCACTAGTTA[C/G]GAGGTGACCGAGTAG | 8208 |
rs1906485 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396664 | TTCCttttttttttt[C/T]ttttttttttgagac | 8208 |
rs1906486 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396663 | TCCtttttttttttc[C/T]tttttttttgagaca | 8208 |
rs1906487 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396603 | gcagtggcgccgtca[A/G]agctcactgcagcct | 8208 |
rs2129798 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417118 | cgccactgcactcca[A/G]cctgggcaacagagc | 8208 |
rs2269187 | snp | A/G | 0.496778 | 0.0400063 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389066 | GGGGTAAGATCCCGC[A/G]TCGGTACCCAGCTTG | 8208 |
rs2633325 | snp | A/T | 0.00477324 | 0.0486193 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376317 | AAAATATGGTTCTAA[A/T]ATATACATAGTTTAT | 8208 |
rs2835341 | snp | G/T | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393837 | ATCTCATTTTAATGC[G/T]TAGTTCTGGAGATTG | 8208 |
rs2835342 | snp | G/T | 0.124491 | 0.216211 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414379 | CATAATATGTGTATG[G/T]GTTGCTGGCTTTAAC | 8208 |
rs2845757 | snp | A/G | 0.280256 | 0.248162 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378492 | tgaggtcaggagatc[A/G]agaccatcctggcca | 8208 |
rs2850081 | snp | C/T | 0.440599 | 0.161778 | | | GRCh38.p7 | 21:36377391 | GGAAGCACTTAGATA[C/T]TTTTTGCTCTTTATG | 8208 |
rs3787734 | snp | A/G | 0.0335098 | 0.125028 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414068 | CAGTGTGGCTGGCAC[A/G]CACGCCTGTGTCTGC | 8208 |
rs7275524 | snp | A/G | 0.137867 | 0.223442 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417197 | ccacctcagcttccc[A/G]agtagctgggactac | 8208 |
rs7278517 | snp | C/T | 0.0501905 | 0.150254 | | | GRCh38.p7 | 21:36377274 | CCTTTTGGCCAGCTT[C/T]TCTATGTATTCTTGC | 8208 |
rs7278581 | snp | A/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399433 | TGAAAACTGTTGCGG[A/T]GGTAATAGGCTGTTG | 8208 |
rs7278593 | snp | A/G | 0.00953873 | 0.0683987 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377111 | caagagcgaaactcc[A/G]tctcaaaaaaaaaGG | 8208 |
rs7279180 | snp | C/T | 0.127944 | 0.218179 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407080 | GCCAAGGTGGGTGGA[C/T]CACCTGAGGTCTGGA | 8208 |
rs7281977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398640 | gctgggattacaggc[A/G]tgagccacctcgccc | 8208 |
rs7282109 | snp | C/G | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398712 | ATAAACTATTTTTGT[C/G]CTTTCTGAAAAGAAG | 8208 |
rs7282284 | snp | A/G | 0.00140614 | 0.0264782 | | | GRCh38.p7 | 21:36377431 | AAGTATTGCCAAGAT[A/G]TGAGACTTCGAAAAT | 8208 |
rs7509895 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383806 | ggcgcccgccgccac[A/G]cccgactaatttttt | 8208 |
rs8126861 | snp | A/G | 0.168135 | 0.236216 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388546 | ATCTTGGCTCACTGC[A/G]ACCTCTGCCTCCCAG | 8208 |
rs8127277 | snp | C/T | 0.216048 | 0.247684 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394100 | tttttttttttgaga[C/T]ggagtctcactctgt | 8208 |
rs8127381 | snp | A/T | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396182 | tttttgtatttttag[A/T]agagatggggtttgc | 8208 |
rs8127711 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396112 | ttcaacaattctcct[A/G]cctcagccctcaagg | 8208 |
rs8127746 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396202 | atggggtttgcccat[A/G]ttggccaggctggtc | 8208 |
rs8128974 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392402 | attcgacaaaaccgc[C/G]atcgtcatcatggcc | 8208 |
rs8129103 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392460 | tcccagacggggtgg[C/T]ggccgggtagagggg | 8208 |
rs8129295 | snp | C/T | 0.216349 | 0.247725 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390666 | gatatattgttatcc[C/T]catttttgagacagg | 8208 |
rs8129487 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392526 | cgccccccacctccc[A/G]gacggggcagctggc | 8208 |
rs8129667 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401337 | tttaatatgttatat[A/T]tttatattatatata | 8208 |
rs8130019 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378488 | atcatgaggtcagga[G/T]atcgagaccatcctg | 8208 |
rs8130294 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392593 | gctgccgggcagaga[C/T]gctcctctcttccca | 8208 |
rs8132242 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382620 | tcttggctcactgcc[C/T]tctgggttcaagtga | 8208 |
rs8133286 | snp | C/G | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398879 | ATTGAATATAAGATG[C/G]CCTTGGAATAAAAGT | 8208 |
rs9754126 | snp | A/G | 0.274736 | 0.248773 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389761 | AGTGCATGAAGGGAT[A/G]TGTGTGTGTGTGTGT | 8208 |
rs9754297 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376755 | GCAGTTTATTTTTTG[A/G]AGACTGTTTCCATTA | 8208 |
rs9754317 | snp | G/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376754 | TGCAGTTTATTTTTT[G/T]AAGACTGTTTCCATT | 8208 |
rs9978761 | snp | A/G | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404879 | ctcctgagtagctga[A/G]attacaggcgcctgc | 8208 |
rs10483033 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405327 | tatataaaaattcct[A/G]tctttcgtctatatt | 8208 |
rs10529380 | in-del | -/T | 0 | 0 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379904 | TTTTTTTTTTTTTTT[-/T]GAAACAAAGTATCAT | 8208 |
rs11088346 | snp | A/G | 0.067446 | 0.170804 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403551 | TATGGAAGCCATAGC[A/G]CTAAAGCCAAAGATA | 8208 |
rs11280868 | in-del | -/GCAACCTCC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382616 | TGATCTTGGCTCACT[-/GCAACCTCC]GCCCTCTGGGTTCAA | 8208 |
rs11701086 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386562 | acgatcactccactg[C/G]actccagcctgggtg | 8208 |
rs11701134 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386748 | agacggagtcttgct[C/T]tgttgcccaggtggg | 8208 |
rs12151974 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382560 | tttttttttttttca[A/G]actgagtctgtttct | 8208 |
rs12627489 | snp | A/G | 0.330482 | 0.236691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394207 | tcaccctcctgagta[A/G]ctgggtctgcaggtg | 8208 |
rs13046055 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407214 | gcctgaggcaggaga[A/C]tcgctccaacccagg | 8208 |
rs13046137 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407071 | ctctgggaggccaag[G/T]tgggtggatcacctg | 8208 |
rs13046178 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407256 | gcagtgagccaagat[C/T]gcaccactgcactct | 8208 |
rs13046248 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407156 | aaaatacaaaaatta[C/G]ccgggcatggtgatg | 8208 |
rs13046340 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407257 | cagtgagccaagatc[C/G]caccactgcactcta | 8208 |
rs13046392 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392865 | ccaaggcaggcggct[G/T]ggaggtggaggttgt | 8208 |
rs13046430 | snp | C/G | 0.326741 | 0.23793 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400292 | TGGGACTGGCCTGGC[C/G]AACATGGTGAAACCC | 8208 |
rs13046747 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407072 | tctgggaggccaagg[G/T]gggtggatcacctga | 8208 |
rs13047955 | snp | G/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379134 | ATCCACAGTAGGTTG[G/T]Ctttttttttttttt | 8208 |
rs13048698 | snp | C/G | 0.497829 | 0.0328757 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389988 | CAGGGCCAATGGCAT[C/G]TTAACCAAGCTCCCA | 8208 |
rs13049605 | snp | C/T | 0.327211 | 0.237778 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400540 | CCCCAACCTGAGTGG[C/T]GTGATTCACTTGGCT | 8208 |
rs13050414 | snp | C/T | 0.366473 | 0.221211 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399288 | TGATTCACCCGCCTC[C/T]GCCTCCCAAAGTGTC | 8208 |
rs13051031 | snp | G/T | 0.011928 | 0.0763002 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379865 | ATTTGGCTGTAGTTC[G/T]TTTTTTTTTtttttt | 8208 |
rs13053082 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407115 | aagaccagcctggcc[A/C]acatggcaaaaccct | 8208 |
rs13053094 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407146 | gtctctactaaaaat[A/T]caaaaattagccggg | 8208 |
rs16994052 | snp | C/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375674 | TATTTTTCTCTAAGT[C/G]GAGGGCTATGCCATA | 8208 |
rs16994069 | snp | G/T | 0.0696718 | 0.173152 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417024 | TTCATATGCAATTTG[G/T]TATCTAAATAGGTTA | 8208 |
rs28361428 | snp | A/G | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391972 | TGGGTGTTTCTCGGA[A/G]AGGGGGATTTGGCAG | 8208 |
rs28576459 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392106 | TCCCTGGGTACTTGA[A/G]ATTAGGGAGTGGTGA | 8208 |
rs28691871 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405276 | TAGTATTAGAATTTT[A/T]AAAATAATTTGATAA | 8208 |
rs34332851 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409296 | TGAGCCACCGCGCCC[-/C]TGCCAAAATGTTTAC | 8208 |
rs34390263 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411779 | GTCACCCAGGCTGGA[-/A]GTGCAGTGGTGTGAT | 8208 |
rs34476947 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415690 | TGTGGAGGACTGTCC[-/C]TGTGTATTATGCGAT | 8208 |
rs34638024 | in-del | -/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382557 | TTTTTTTTTTTTTTT[-/T]CAGACTGAGTCTGTT | 8208 |
rs34926522 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388488 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTG | 8208 |
rs35051347 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402914 | TGTCTGCTCCCGTTT[-/T]ACGCTGCAGCTTATC | 8208 |
rs35343767 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415721 | TTTAACAGCATCCCC[-/C]GGCTGCTACTTCTTG | 8208 |
rs35488336 | in-del | -/T | 0.359998 | 0.2245 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411117 | TTCTTATAAATATTC[-/T]TTTTTTTTTTTTTTG | 8208 |
rs35580662 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410418 | CCATTACACATGTAT[-/T]ATATTAGGTCCTTTG | 8208 |
rs35604187 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398250 | GTAAAGATGGGATTT[-/T]GCCATGTTGCCCAGG | 8208 |