SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12066 | snp | A/G | 0.49306 | 0.0584955 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613974 | cgttaggcatgtggc[A/G]aaaacgttggggtac | 142678 |
rs1127870 | snp | C/G | 0 | 0 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613797 | TCCTTTCTTGGATTC[C/G]CTGTGTAAACGAAAA | 142678 |
rs3935032 | snp | C/T | 0.25634 | 0.24992 | intron-variant | MIB2 | GRCh38.p7 | 1:1628814 | TGTCCACCTTCCCCT[C/T]CAGTGATGGCCCAGG | 142678 |
rs4648611 | snp | C/T | 0.498964 | 0.02274 | upstream-variant-2KB, utr-variant-5-prime | MIB2 | GRCh38.p7 | 1:1615322 | GCGCAGTGGCGGTCC[C/T]AGAGACGCACTCGGT | 142678 |
rs4648781 | snp | A/G | | | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614505 | ctatctgagagggcc[A/G]ggcgaaggggaaaat | 142678 |
rs6604985 | snp | A/G | 0.496314 | 0.0427728 | intron-variant | MIB2 | GRCh38.p7 | 1:1617375 | GGAGAGAGTTCCCTT[A/G]TTGCAAGTATTTTAT | 142678 |
rs7366874 | snp | A/G | | | intron-variant | MIB2 | GRCh38.p7 | 1:1621214 | NNNNNNNNNCCATGG[A/G]CCCCTGTGGCACTAT | 142678 |
rs7366875 | snp | A/G | | | intron-variant | MIB2 | GRCh38.p7 | 1:1621176 | GCGGGGCCTTTGAGA[A/G]CAGCCCCCAGGTGGT | 142678 |
rs7418389 | snp | A/G | 0.469839 | 0.119041 | missense, utr-variant-5-prime, nc-transcript-variant, synonymous-codon | MIB2 | GRCh38.p7 | 1:1616547 | GCCCTGATGCCTGGA[A/G]ACTTTGGGACTGGCC | 142678 |
rs7519863 | snp | C/G | 0.0644693 | 0.167566 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613516 | aactcctgggctatg[C/G]tgtttgctcacctct | 142678 |
rs7529236 | snp | C/T | | | intron-variant | MIB2 | GRCh38.p7 | 1:1621182 | CCCCTCGCGGGGCCT[C/T]TGAGAACAGCCCCCA | 142678 |
rs7543265 | snp | C/T | 0.406296 | 0.19512 | intron-variant | MIB2 | GRCh38.p7 | 1:1620609 | GCAGCAGTCTGCTGG[C/T]GGGGGGACAAGTGAG | 142678 |
rs9329576 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | MIB2 | GRCh38.p7 | 1:1619986 | GGGGCAGTGGGGTGG[A/G]GTGCCAAGGCCATCA | 142678 |
rs9442410 | snp | C/G | 0.496279 | 0.0429702 | intron-variant | MIB2 | GRCh38.p7 | 1:1618290 | TCTGTTCTACACCCA[C/G]AAGGCTCCAGGTGCA | 142678 |
rs9442425 | snp | C/T | 0.493925 | 0.054776 | intron-variant | MIB2 | GRCh38.p7 | 1:1618982 | ACCCAAGACCTGCCA[C/T]TGGGCTCCTGGCACC | 142678 |
rs9442427 | snp | A/G | | | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614737 | gagccaccgcgcccg[A/G]ccTCTCATTTCTTAA | 142678 |
rs9442430 | snp | A/G | 0.498794 | 0.0245311 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613421 | gaggctgaggagggc[A/G]gatcacttgaggtca | 142678 |
rs9442431 | snp | A/G | 0.499104 | 0.0211472 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613322 | aaaaaaatattagcc[A/G]ggcatggtggtgcac | 142678 |
rs9726211 | snp | C/T | 0.499104 | 0.0211472 | intron-variant, utr-variant-5-prime, missense, upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1615869 | CAGCTCCCGGCAGGC[C/T]TCGCGCGGCCCGGGG | 142678 |
rs9793820 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | MIB2 | GRCh38.p7 | 1:1622513 | CATCCCTGCCTCCGG[C/T]AGCCTGGATTTGCAC | 142678 |
rs11544452 | snp | A/G | 0.297975 | 0.245354 | synonymous-codon, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1627156 | GGTGGTGGAGGTGGC[A/G]CTGGGTAACGCAGCC | 142678 |
rs11556213 | snp | A/G | | | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614063 | ATTATTAACTCAAAA[A/G]AAAAAAAAAGATTGT | 142678 |
rs12725787 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | MIB2 | GRCh38.p7 | 1:1620016 | CTGTGACGCGGGGGC[C/T]GCCAAGGCTTGGTCT | 142678 |
rs12727853 | snp | C/G | | | synonymous-codon, intron-variant, missense | MIB2 | GRCh38.p7 | 1:1623662 | CGCCGGCTACCAGGG[C/G]GCGCACGACCTGCTG | 142678 |
rs12727988 | snp | G/T | | | splice-donor-variant, intron-variant | MIB2 | GRCh38.p7 | 1:1623701 | CAACGCCCAGATCGG[G/T]GCGCGCCAAGGGCAG | 142678 |
rs12735861 | snp | C/T | 0.49533 | 0.0480965 | intron-variant | MIB2 | GRCh38.p7 | 1:1627515 | GGCCTGGGAGGGGCC[C/T]GGCCGGCGGGGCTGA | 142678 |
rs12748433 | snp | C/T | 0.303438 | 0.244222 | intron-variant | MIB2 | GRCh38.p7 | 1:1624591 | GGTTCGCTCCAGGCC[C/T]CTGAGCCCAGGGGCA | 142678 |
rs12755088 | snp | C/T | 0.211826 | 0.247338 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | MIB2 | GRCh38.p7 | 1:1623412 | CAGCCCGGCCCACCA[C/T]GGACCCCTCTGCCCA | 142678 |
rs28414017 | snp | A/C/T | 0.0201107 | 0.098239 | synonymous-codon, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1623847 | GCGCTGGAAGTGCCG[A/C/T]GTGTGCCTGGACTAC | 142678 |
rs28430872 | snp | C/T | 0.0581099 | 0.160244 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614225 | CTAAACAAATGGAGT[C/T]GGGAGGCCACGAAGG | 142678 |
rs28441531 | snp | A/C | | | intron-variant | MIB2 | GRCh38.p7 | 1:1622278 | CCCCTCCCCGCCAGG[A/C]TGGAGTGTAGTGGTG | 142678 |
rs28441650 | snp | A/G | 0.257176 | 0.249897 | intron-variant | MIB2 | GRCh38.p7 | 1:1624720 | CTGCTCCACTGCATC[A/G]CTCTCCCAAGTGGCT | 142678 |
rs28464684 | snp | C/T | 0.216349 | 0.247725 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MIB2, MMP23B | GRCh38.p7 | 1:1630781 | GGGCCAGGACACCCT[C/T]CAGGCGCGGGCACGG | 142678 |
rs28475060 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | MIB2 | GRCh38.p7 | 1:1617194 | TCCATGGCCTGTGGC[A/G]TGCCACACACAGCGG | 142678 |
rs28502067 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | MIB2 | GRCh38.p7 | 1:1616717 | TTTGTGTCTGAGCAT[A/G]CATGCGAGTGGAGGG | 142678 |
rs28510084 | snp | C/G | 0.460026 | 0.13567 | intron-variant | MIB2 | GRCh38.p7 | 1:1627057 | CTGGCCACCACTAAC[C/G]TCAGCCCTGCCCCCA | 142678 |
rs28546565 | snp | A/G | 0.263809 | 0.249618 | intron-variant | MIB2 | GRCh38.p7 | 1:1618118 | TGGGCTGTGGCTGTG[A/G]CTGTCTCTGGTTTGT | 142678 |
rs28550511 | snp | G/T | | | intron-variant | MIB2 | GRCh38.p7 | 1:1622312 | TCACAGCCAGCTGTA[G/T]CCTCCACCTTCTGAT | 142678 |
rs28570192 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | MIB2 | GRCh38.p7 | 1:1620261 | GCAGAGACAGAAGGC[A/G]CCCCCTGCTGCAGAA | 142678 |
rs28601681 | snp | A/G | 0.177824 | 0.239355 | intron-variant | MIB2 | GRCh38.p7 | 1:1618792 | GGGCTGGATCCTCCC[A/G]CCCCTAAGCAGGTGC | 142678 |
rs28617190 | snp | A/G | 0.448963 | 0.151372 | intron-variant | MIB2 | GRCh38.p7 | 1:1624086 | CCGTGGCCTTAAGCA[A/G]TGGTGCCATGGGCAG | 142678 |
rs28623434 | snp | C/G | 0.496279 | 0.0429702 | intron-variant | MIB2 | GRCh38.p7 | 1:1618213 | CATAGCAGCCTCTGG[C/G]CCAGAGCTCACCCGC | 142678 |
rs28635343 | snp | C/T | 0.365232 | 0.22186 | intron-variant | MIB2 | GRCh38.p7 | 1:1624723 | CTCCACTGCATCGCT[C/T]TCCCAAGTGGCTCAA | 142678 |
rs28681667 | snp | G/T | 0.0192683 | 0.096244 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | MIB2 | GRCh38.p7 | 1:1623829 | GCACGGGCTGCGGGG[G/T]ATGCGCTGGAAGTGC | 142678 |
rs28689170 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | MIB2 | GRCh38.p7 | 1:1618288 | TCTGCACCTGGAGCC[C/T]TGTGGGTGTAGAACA | 142678 |
rs28710339 | snp | C/G | 0.398894 | 0.200825 | intron-variant | MIB2 | GRCh38.p7 | 1:1622295 | GGAGTGTAGTGGTGC[C/G]ATCACAGCCAGCTGT | 142678 |
rs28714563 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | MIB2 | GRCh38.p7 | 1:1622900 | TACGGCGCCTGCATC[A/G]TGTTTGCCGTTTTTC | 142678 |
rs28730454 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MIB2, MMP23B | GRCh38.p7 | 1:1630688 | AGCCTGGGGGCGAGG[A/G]GGGGGGGCCCTTCCC | 142678 |
rs34024794 | in-del | -/T | | | intron-variant | MIB2 | GRCh38.p7 | 1:1622300 | AGGCTACAGCTGGCT[-/T]GTGATCGCACCACTA | 142678 |
rs34047429 | in-del | -/C | | | intron-variant | MIB2 | GRCh38.p7 | 1:1621268 | GCCCTCGGAGGCCCC[-/C]GCGGAGCCAGGAGCC | 142678 |
rs34065885 | in-del | -/T | | | intron-variant | MIB2 | GRCh38.p7 | 1:1619091 | CCACTGTGCCCGGCC[-/T]GCCAGCAGCTTTTGA | 142678 |
rs34329439 | in-del | -/T | | | intron-variant | MIB2 | GRCh38.p7 | 1:1621278 | ACCCCACCTTGCCCT[-/T]CGGAGGCCCCGCGGA | 142678 |
rs34424150 | in-del | -/G | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | MIB2 | GRCh38.p7 | 1:1615501 | TGTGGGACCCGAAGG[-/G]CGGGAGCCCAGGGCC | 142678 |
rs34501155 | snp | A/G | 0.292266 | 0.246401 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613769 | AAAATAAAATCCTAA[A/G]CTCTCTACCAACTGT | 142678 |
rs34983251 | snp | C/T | 0.426354 | 0.177198 | intron-variant | MIB2 | GRCh38.p7 | 1:1621352 | CCCTCCCCACGGCCT[C/T]CTGCAGCCTCCCGGC | 142678 |
rs35508925 | in-del | -/G | | | intron-variant | MIB2 | GRCh38.p7 | 1:1618921 | AGGCCTCTCTAGGGG[-/G]TGTTTGTGGTGGGGG | 142678 |
rs35678255 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1623904 | GTCGAAGGCGTGGGC[-/T]GAGCTCATGCTTGTT | 142678 |
rs35720036 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1628161 | GCGTGACCCTTGAGG[-/G]AGGCATGGTGCAGCA | 142678 |
rs35950085 | in-del | -/G | | | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613253 | AATTGCTTGAGCCCA[-/G]GAGGTGGAGGTTGCA | 142678 |
rs61774905 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MIB2 | GRCh38.p7 | 1:1619307 | GTGAACTTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 142678 |
rs61774907 | snp | G/T | 0.485319 | 0.0844083 | intron-variant | MIB2 | GRCh38.p7 | 1:1629332 | TCCGTGGACGGCGGG[G/T]ATGGGGTCCGGCGGC | 142678 |
rs61774908 | snp | C/T | 0.340784 | 0.232934 | intron-variant, upstream-variant-2KB, downstream-variant-500B | MIB2, MMP23B | GRCh38.p7 | 1:1630798 | AGGCGCGGGCACGGC[C/T]GCCTCCCGCCCCCCA | 142678 |
rs66599757 | snp | A/G | 0.408017 | 0.193729 | intron-variant, missense | MIB2 | GRCh38.p7 | 1:1625951 | GGGCGGGAGGGAGGC[A/G]GCTGGGCTAAGATGC | 142678 |
rs70937159 | in-del | -/T | 0 | 0 | | | GRCh38.p7 | 1:1613179 | TTTTTTTTTTTTTTT[-/T]GAGACGGATTCTTGC | 142678 |
rs70937160 | in-del | -/A | 0.322007 | 0.239405 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1615016 | CGAGGCTCCGTCTCC[-/A]AAAAAAAAAAAAGAA | 142678 |
rs70937161 | in-del | -/T | 0.457037 | 0.140127 | intron-variant | MIB2 | GRCh38.p7 | 1:1624324 | ACCCCGTCCCCTGCA[-/T]TTGTCACCTTTGTCT | 142678 |
rs72634815 | snp | C/T | 0.0869089 | 0.189476 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614340 | TACTGCAGGGAAATT[C/T]CTCAGGACTGCAGTA | 142678 |
rs72634816 | snp | C/T | 0.247905 | 0.249991 | intron-variant | MIB2 | GRCh38.p7 | 1:1622510 | CTCCATCCCTGCCTC[C/T]GGCAGCCTGGATTTG | 142678 |
rs72634817 | snp | A/G | 0.259397 | 0.249823 | intron-variant | MIB2 | GRCh38.p7 | 1:1625805 | GACTGGTGGGTGGAG[A/G]TGGGTGGGGTCAAGG | 142678 |
rs72897886 | snp | C/T | 0.136506 | 0.222754 | intron-variant | MIB2 | GRCh38.p7 | 1:1624205 | AGGACAGCCCATACC[C/T]GGAGCCAGCACCTGG | 142678 |
rs72897888 | snp | C/T | 0.0213713 | 0.101138 | intron-variant | MIB2 | GRCh38.p7 | 1:1625464 | GCCCTGTGTGCCCTG[C/T]CCTCCCAGCCCTCCG | 142678 |
rs72897889 | snp | C/T | 0.0196826 | 0.0972312 | intron-variant | MIB2 | GRCh38.p7 | 1:1625478 | GCCCTCCCAGCCCTC[C/T]GCCCCCTCAGCCCCT | 142678 |
rs74045801 | snp | C/T | 0.15665 | 0.231917 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614531 | GATAGGCCTATGATC[C/T]GTCATGGCACGAACA | 142678 |
rs74047804 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | MIB2 | GRCh38.p7 | 1:1617651 | GGTAGCCGAGCGAAT[C/G]TGTGACCCAGGAAGT | 142678 |
rs74047806 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MIB2 | GRCh38.p7 | 1:1620249 | GAGAGTCTGGGCGCA[A/G]AGACAGAAGGCGCCC | 142678 |
rs74047807 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | MIB2 | GRCh38.p7 | 1:1621536 | GGTGAGGGAGGCAGC[A/G]TCACCCGACAGGTGA | 142678 |
rs74047808 | snp | A/G | 0.00370365 | 0.0428732 | missense, nc-transcript-variant, intron-variant | MIB2 | GRCh38.p7 | 1:1626711 | TTGACACAGTGAAGC[A/G]GCTGCAGGCTGGGCA | 142678 |
rs74047811 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | MIB2 | GRCh38.p7 | 1:1627891 | GTCCCTGGCCTGGGT[G/T]CCCTCTGCCCATGTG | 142678 |
rs74047812 | snp | C/T | 0.00633913 | 0.0559409 | synonymous-codon, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1628021 | TCCGCCCCAGCAGGA[C/T]GCCCACTCGGACACG | 142678 |
rs74465618 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | MIB2 | GRCh38.p7 | 1:1617873 | GGGTAGATGGCAAAG[G/T]CTAGCATTTCTGGCA | 142678 |
rs74735770 | snp | A/C | 0.0995161 | 0.199636 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614370 | ATTCTAGATAAGCAG[A/C]TTGCACAAGGACGTC | 142678 |
rs74808013 | snp | A/G | 0.00731226 | 0.0600222 | missense, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1627725 | GGGTGCCGGGCGGAC[A/G]CCATCAACAGCACCC | 142678 |
rs74892851 | snp | A/C | 0.408466 | 0.193405 | intron-variant | MIB2 | GRCh38.p7 | 1:1628409 | CGGGAGGTGCGGACG[A/C]GGCCCAGTCCTGCCC | 142678 |
rs75109477 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613786 | TAGGATTTTATTTTT[C/T]GTTTACACAGGGAAT | 142678 |
rs75147751 | snp | C/T | 0.00629807 | 0.0557617 | synonymous-codon, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1627322 | GAACCAAGGCAGGAC[C/T]GCTCTGCAAGTGGCT | 142678 |
rs75377981 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1613686 | TGCAGTCAACCAAGA[C/T]AGTGCCACTGCACTC | 142678 |
rs75855249 | snp | C/T | 0.00624819 | 0.0555433 | synonymous-codon, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1627406 | CGTGGACCTGCCGGA[C/T]GACGAGGGCAACACG | 142678 |
rs76008910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MIB2 | GRCh38.p7 | 1:1621086 | GATTCTCTCTGGTTC[C/T]TATGTTTCATTCATG | 142678 |
rs76837904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MIB2 | GRCh38.p7 | 1:1623114 | CTGTGGGAAGAGATG[A/G]TGGTTTTCTTCCGAG | 142678 |
rs76957527 | snp | C/T | 0.00774509 | 0.0617459 | missense, nc-transcript-variant | MIB2 | GRCh38.p7 | 1:1627720 | GTGCTGGGTGCCGGG[C/T]GGACGCCATCAACAG | 142678 |
rs77051740 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MIB2 | GRCh38.p7 | 1:1614702 | CAGGGACCTTCTCCG[G/T]AAGTACGCAATGTCT | 142678 |
rs77170202 | snp | C/G | 0.5 | 0 | intron-variant | MIB2 | GRCh38.p7 | 1:1626309 | ATGGTCCTGGGGCCC[C/G]ACCCCCACGCTGGCT | 142678 |
rs77432776 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | MIB2 | GRCh38.p7 | 1:1621801 | GCCGGGGCACGGATC[C/G]GGGGCACGGATCGGG | 142678 |
rs77523903 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | MIB2 | GRCh38.p7 | 1:1625992 | TGCTGTATGGGGGCC[A/G]ATGGGGGTGGCTGGT | 142678 |
rs78656035 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | MIB2 | GRCh38.p7 | 1:1620338 | TCCTTCATCTCCATT[A/G]CCGGGCCCATCTCGG | 142678 |
rs79366324 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | MIB2 | GRCh38.p7 | 1:1622264 | TGAGTGGTGGCCCTC[C/T]CCTCCCCGCCAGGCT | 142678 |
rs79372291 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | MIB2 | GRCh38.p7 | 1:1622382 | AGACTGTGCTGAAGC[C/T]CAGCATGGTGGAGAG | 142678 |
rs79432957 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | MIB2 | GRCh38.p7 | 1:1624213 | CCATACCCGGAGCCA[A/G]CACCTGGGCTGTCTT | 142678 |
rs79765738 | snp | A/C/G | 0.0122204 | 0.07721 | intron-variant | MIB2 | GRCh38.p7 | 1:1624755 | ATGGGAAGAGATGGC[A/C/G]GTTTTCTTCTGAGAG | 142678 |
rs79836664 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MIB2 | GRCh38.p7 | 1:1617490 | GCAATAGAACAGACC[C/T]GGTGTCTGCTTGCGT | 142678 |