SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1317082 | snp | A/G | 0.391583 | 0.206044 | intron-variant | MYNN | GRCh38.p7 | 3:169779797 | TCCCTCCAAATAAGT[A/G]TGTTGATTCTAGCTT | 55892 |
rs1881966 | snp | A/G | 0.431473 | 0.171952 | intron-variant | MYNN | GRCh38.p7 | 3:169778152 | GGAGTTGAAGGCTGC[A/G]GTGAGTTATCATTAT | 55892 |
rs1920120 | snp | C/T | 0.487933 | 0.0767327 | intron-variant | MYNN | GRCh38.p7 | 3:169784392 | AGATACATTTCTGTT[C/T]ATGAAAATGCTCAAG | 55892 |
rs1920121 | snp | A/G | 0.0482946 | 0.147699 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169787865 | TGCCACTTTTCCCAC[A/G]TATTAATTTATTTCA | 55892 |
rs1920122 | snp | C/T | 0.487558 | 0.0778863 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169788353 | TCTATGCATGTGTAT[C/T]AAGTTAAAATAGTGG | 55892 |
rs1920123 | snp | C/T | 0.487558 | 0.0778863 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169788385 | TTTAAATACAATTTA[C/T]AAAGCATTAGAATGT | 55892 |
rs2068178 | snp | A/G | 0.0755905 | 0.179113 | missense | ACTRT3 | GRCh38.p7 | 3:169767851 | AAACCCGATTGTCTA[A/G]AGAAAGTTTACCAAC | 55892 |
rs2141595 | snp | C/T | 0.496714 | 0.0404017 | intron-variant | MYNN | GRCh38.p7 | 3:169785644 | TCCGGGCAGAGAACA[C/T]TGTAGAGAGTCAGTG | 55892 |
rs2251795 | snp | A/T | 0.408359 | 0.193449 | intron-variant, upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169773941 | TAGTGGTTTAAAAAA[A/T]TTTTTTGTAACATAA | 55892 |
rs3046465 | in-del | -/ATC | 0.391583 | 0.206044 | intron-variant | MYNN | GRCh38.p7 | 3:169778160 | AGGCTGCGGTGAGTT[-/ATC]ATTATACCAGTGCAC | 55892 |
rs3772188 | snp | C/T | 0.0479149 | 0.147179 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169787159 | CTAAATTTTTACGAG[C/T]GAAAATATGAAATTT | 55892 |
rs3772190 | snp | C/T | 0.391397 | 0.206172 | intron-variant | MYNN | GRCh38.p7 | 3:169782699 | TAAAAGGCCCAAGTC[C/T]CCTTTTTCTTTTATT | 55892 |
rs3821383 | snp | C/T | 0.488545 | 0.074807 | upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169772158 | CTCAAGTGATTATTA[C/T]CAAATTGAGAGGAAT | 55892 |
rs3950296 | snp | C/G | 0.391583 | 0.206044 | intron-variant | MYNN | GRCh38.p7 | 3:169775495 | ATCTTTCCTGTCAGT[C/G]GCTATGTCTCCTTGA | 55892 |
rs4618260 | snp | A/C | 1.64953e-05 | 0.00287182 | missense | ACTRT3 | GRCh38.p7 | 3:169767662 | AGGTTGATCCCCCGG[A/C]AAGGATAATATTGGA | 55892 |
rs7624848 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169786703 | GAATATGGAATTGCT[A/G]AGATATCATTGGTAG | 55892 |
rs7626989 | snp | A/C | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771263 | attatatttatatat[A/C]ataaatatataaaaa | 55892 |
rs7634517 | snp | C/G | 0 | 0 | intron-variant | MYNN | GRCh38.p7 | 3:169786280 | GTGAGGAGGGCATAT[C/G]TACAAAAGAGAAACC | 55892 |
rs7634698 | snp | A/G | | | synonymous-codon, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169786468 | TACTTTGAGTGAACA[A/G]GATTCCATACAAAAA | 55892 |
rs9811216 | snp | C/T | 0.472803 | 0.113397 | utr-variant-5-prime | ACTRT3 | GRCh38.p7 | 3:169769713 | CCGTGCTCCTCATGT[C/T]ACCGCCCGCTATTGC | 55892 |
rs9822885 | snp | A/G | 0.461202 | 0.133767 | intron-variant | ACTRT3 | GRCh38.p7 | 3:169768356 | CACTGGGTAACTGTA[A/G]GGAAAGCAATAAGAT | 55892 |
rs9823758 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ACTRT3 | GRCh38.p7 | 3:169768944 | CAATTGAAGAGAATA[A/G]CCCAAGTGACAAAAG | 55892 |
rs9826466 | snp | A/C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169772313 | aaacacACTAAAAAA[A/C/T]CCCtttttttttttt | 55892 |
rs9833597 | snp | A/G | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770457 | ttatatttatatatc[A/G]taaatataaatatat | 55892 |
rs9833619 | snp | A/G | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770494 | ttatatttatatatc[A/G]taaatataaatatat | 55892 |
rs9833638 | snp | A/G | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770531 | ttatatttatatatC[A/G]taaatataaatatat | 55892 |
rs9833790 | snp | A/G | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770568 | ttatatttatatatc[A/G]taaatatataaaaat | 55892 |
rs9838385 | snp | A/T | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771155 | ataaatatataaaaa[A/T]ttatatttatatatc | 55892 |
rs9838401 | snp | A/T | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771186 | ataaatatataaaaa[A/T]ttatatttatatatc | 55892 |
rs9838416 | snp | A/T | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771217 | ataaatatataaaaa[A/T]ttatatttatatatc | 55892 |
rs9838561 | snp | A/T | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771305 | atataataaatatat[A/T]aaaaattatgtttat | 55892 |
rs9840387 | snp | G/T | 0.0123036 | 0.0774623 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169787442 | TTTATGTTTTATTCC[G/T]TTCTAAAATATTGGA | 55892 |
rs9853966 | snp | C/T | 0.0123036 | 0.0774623 | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169786977 | TGCATTTTAGAATTG[C/T]CCTTCATTTACTAAA | 55892 |
rs9855337 | snp | A/G | 0.084364 | 0.187256 | intron-variant | MYNN | GRCh38.p7 | 3:169774702 | TGTTTTTATAAAGAA[A/G]TCAGTATCACTGATT | 55892 |
rs9860874 | snp | A/C | 0.489837 | 0.0705577 | intron-variant | ACTRT3 | GRCh38.p7 | 3:169768483 | CACAGCCTCTCACAG[A/C]AGGTAAGTGTCAGCC | 55892 |
rs9866116 | snp | A/G | 0.497907 | 0.0322805 | intron-variant | MYNN | GRCh38.p7 | 3:169776839 | CTCCCGAGTAGCTGG[A/G]ATTACAGGCACCCGC | 55892 |
rs9866557 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-5-prime | ACTRT3 | GRCh38.p7 | 3:169769581 | ACGGGCTCGGCCGGG[A/G]CCGAGTGCCTGGAAC | 55892 |
rs9866776 | snp | A/C | 0.488363 | 0.0753851 | utr-variant-5-prime | ACTRT3 | GRCh38.p7 | 3:169769863 | CCAGAAGAGCTATAA[A/C]AGCAGTTTTATTTTC | 55892 |
rs9874233 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | MYNN | GRCh38.p7 | 3:169783224 | TCATATAAAAATCAA[A/G]TTCCTTGCCCAAATC | 55892 |
rs9880210 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | MYNN | GRCh38.p7 | 3:169777102 | AATTAGAGACCAAAA[G/T]ATCTTTTTTAGTGGC | 55892 |
rs10576565 | in-del | -/AA | 0.0119091 | 0.0762411 | intron-variant | MYNN | GRCh38.p7 | 3:169775366 | GGAGGGAATAAAAGC[-/AA]AGAGAAACTGATTAA | 55892 |
rs10681957 | in-del | -/TTT | | | intron-variant | MYNN | GRCh38.p7 | 3:169776695 | TTTTTTTTTTTTTTT[-/TTT]TTGAGATGGAGTCTC | 55892 |
rs10936599 | snp | C/T | 0.404747 | 0.19635 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169774313 | GCAGTATTCGCACCA[C/T]TGTGAGCACCTTTTA | 55892 |
rs11293618 | in-del | -/A | | | upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169771962 | CCTTTCCAGGGAGAC[-/A]AAAAAAAAAAAGGCC | 55892 |
rs11336818 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169772317 | ACACTAAAAAATCCC[-/T]TTTTTTTTTTTTTTT | 55892 |
rs11456214 | in-del | -/A | | | intron-variant | MYNN | GRCh38.p7 | 3:169784913 | AAAAAAAAAAAAAAA[-/A]CTTGAAACATTTCCT | 55892 |
rs11553294 | snp | G/T | 0 | 0 | missense, nc-transcript-variant, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169774367 | AGCAGGTTTTCTCTG[G/T]GACTGTACCATAGTG | 55892 |
rs11714841 | snp | A/G | 0.0197644 | 0.0974247 | missense, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169786433 | GCAGATAAAACTCTA[A/G]ACTCCAGTGCAGAGG | 55892 |
rs12637087 | snp | C/G/T | 0.000166289 | 0.00911711 | synonymous-codon, missense | ACTRT3 | GRCh38.p7 | 3:169769383 | GAGTTCTAGCCCGCC[C/G/T]TGGGCCGCGCGGCTC | 55892 |
rs12637184 | snp | A/G | 0.394538 | 0.203982 | utr-variant-5-prime | ACTRT3 | GRCh38.p7 | 3:169769649 | CAGAGTCCTGGGGGC[A/G]CAGGCAGGGGGTCGG | 55892 |
rs13314293 | snp | A/G | 0.0116702 | 0.075491 | intron-variant | MYNN | GRCh38.p7 | 3:169778743 | TTTGATCAGAATATT[A/G]TCATGTAGCCTTGTT | 55892 |
rs16847890 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MYNN | GRCh38.p7 | 3:169777803 | GTAACTCTCACATCA[C/T]GAACACTCCAGCTAA | 55892 |
rs16854368 | snp | C/G/T | 0.0486741 | 0.148216 | intron-variant | MYNN | GRCh38.p7 | 3:169783337 | CATTTACTTGGATCA[C/G/T]TGAAAATACCTCTAA | 55892 |
rs17568472 | snp | A/G | 0.00911815 | 0.0669024 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169774448 | TGAGTATTTTGGTGC[A/G]ATCTACAGAAGCACT | 55892 |
rs17850177 | snp | C/G | | | missense | ACTRT3 | GRCh38.p7 | 3:169768317 | GATCTCCATGTCCTC[C/G]CATGAAGTAATGAGA | 55892 |
rs28371163 | snp | A/C | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771325 | ATTATGTTTATATAT[A/C]ATAAATATAAAAATT | 55892 |
rs28465436 | snp | A/C | 0.433673 | 0.1696 | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771294 | ATTATGTTTATATAT[A/C]ATAAATATATAAAAA | 55892 |
rs28635281 | snp | A/T | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771310 | ATAAATATATAAAAA[A/T]TTATGTTTATATATA | 55892 |
rs28649851 | snp | A/G | 0.466412 | 0.125164 | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771524 | TATATAAAAATTTAT[A/G]TTTATATATAATAAA | 55892 |
rs34022516 | snp | A/G | 0.0195694 | 0.0969626 | intron-variant | MYNN | GRCh38.p7 | 3:169779641 | GAGTACTTAGCACAC[A/G]CTACTTGTGACCAGA | 55892 |
rs34026158 | in-del | -/C | | | intron-variant | MYNN | GRCh38.p7 | 3:169775831 | AAATCTTTCCCTCCC[-/C]TTTTATATTGTAACT | 55892 |
rs34273285 | snp | C/G | 0.026644 | 0.112304 | missense | ACTRT3 | GRCh38.p7 | 3:169767800 | CAGCTCCATGACCAG[C/G]TCTTTTCTTGTCCAG | 55892 |
rs34321597 | snp | A/C | | | intron-variant | MYNN | GRCh38.p7 | 3:169775700 | GAAAAAATAGAAAAA[A/C]CAAAAAAGAAACACC | 55892 |
rs34384341 | in-del | -/A/ATA | 0.00199481 | 0.0315187 | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771333 | ATATATAATAAATAT[-/A/ATA]AAAAATTTGTTTATA | 55892 |
rs34594906 | snp | A/G | 0.00979952 | 0.0693089 | intron-variant | MYNN | GRCh38.p7 | 3:169779611 | ACTGTGACTAATATA[A/G]TGTATTTTTATAGAG | 55892 |
rs34684730 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169787157 | TAAAATTTCATATTT[-/T]CGCTCGTAAAAATTT | 55892 |
rs34847803 | in-del | -/A | 0.394721 | 0.203852 | intron-variant, upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169774228 | CGTTGATGAGAACTT[-/A]ACGGTTACTGATTTA | 55892 |
rs34931136 | snp | C/T | 0.000115545 | 0.00759994 | synonymous-codon | ACTRT3 | GRCh38.p7 | 3:169768161 | TCTGGGTGTTCCTGC[C/T]TTCTATATGTCCATC | 55892 |
rs35100673 | snp | C/T | 0.0547245 | 0.156101 | upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169772149 | ATTATATTCATTCCT[C/T]TCAATTTGATAATAA | 55892 |
rs35197165 | in-del | -/CT/TC | 0.0478135 | 0.14704 | intron-variant | MYNN | GRCh38.p7 | 3:169779769 | CCCTAATGCATCAAC[-/CT/TC]TCCTTATACCATTTT | 55892 |
rs35270580 | snp | C/T | 0.00439002 | 0.0466448 | synonymous-codon | ACTRT3 | GRCh38.p7 | 3:169767885 | TGTGGCAATGAACTA[C/T]GAAGAGGAAATGGCC | 55892 |
rs35283637 | snp | C/G | | | downstream-variant-500B | MYNN | GRCh38.p7 | 3:169789983 | ACATGTGCCATGTTG[C/G]TGTGCTGCACCCATT | 55892 |
rs35294030 | snp | C/T | 0.00134076 | 0.025857 | missense, nc-transcript-variant, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169779040 | GCCTTCTTCTTCTTT[C/T]TCGTTTGAGATGACT | 55892 |
rs35379604 | in-del | -/CAT | | | intron-variant | MYNN | GRCh38.p7 | 3:169778162 | GCTGCAGTGAGTTAT[-/CAT]TATACCAGTGCACTC | 55892 |
rs35406871 | snp | A/G | 0.0262422 | 0.111501 | synonymous-codon, nc-transcript-variant | MYNN | GRCh38.p7 | 3:169782609 | AGTGATAAGAGAACT[A/G]GAGACAGCAAATGCC | 55892 |
rs35419455 | snp | A/G/T | 0.022753 | 0.104207 | missense | ACTRT3 | GRCh38.p7 | 3:169768201 | TGGCCAACCGGCAAC[A/G/T]GATCACGGAAATGTT | 55892 |
rs35446936 | snp | A/G | 0.406641 | 0.194842 | intron-variant | ACTRT3 | GRCh38.p7 | 3:169768720 | TTTTTAGTAGAGACG[A/G]GGTTTCACCGTGTTA | 55892 |
rs35505613 | in-del | -/T | | | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771866 | GAAAGGATGGCTTTT[-/T]CGCGGCTGAATAACG | 55892 |
rs35580600 | in-del | -/A/TA/TGTTTATATATAATAAATATAAAAATT | 0.0678856 | 0.17156 | upstream-variant-2KB | MYNN, ACTRT3 | GRCh38.p7 | 3:169771340 | ATAAATATAAAAATT[lengthTooLong]TGTTTATATATAATA | 55892 |
rs35943960 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169771973 | AGACAAAAAAAAAAA[-/A]GGCCACCCAAAGGAA | 55892 |
rs55656133 | snp | A/G | | | missense | ACTRT3 | GRCh38.p7 | 3:169767676 | GCAAGGATAATATTG[A/G]AAAAGAAGGAATTCC | 55892 |
rs55735727 | snp | A/T | 0.410905 | 0.191336 | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770360 | GAAATATATATATTT[A/T]TATTTATTATATGTA | 55892 |
rs56312325 | in-del | -/AATATA | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770607 | TATATCATAAATATA[-/AATATA]TAAAAATTTATATTT | 55892 |
rs56355715 | in-del | -/AATATA | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770576 | TATATCATAAATATA[-/AATATA]TAAAAATTTATATTT | 55892 |
rs56651288 | snp | G/T | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770678 | AAAAATTTATATTTA[G/T]ATATCATATATAAAA | 55892 |
rs56651316 | snp | A/T | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770714 | TATTTAGATATCATA[A/T]ATAAAAATTTATATT | 55892 |
rs56651385 | snp | G/T | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770705 | AAAAATTTATATTTA[G/T]ATATCATATATAAAA | 55892 |
rs56651412 | snp | A/T | | | upstream-variant-2KB | ACTRT3, MYNN | GRCh38.p7 | 3:169770687 | TATTTAGATATCATA[A/T]ATAAAAATTTATATT | 55892 |
rs57684934 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169772419 | CTGAGGGAAGCCTTA[A/G]CTTAATGTATGCCGG | 55892 |
rs58083088 | snp | A/G | | | intron-variant | MYNN | GRCh38.p7 | 3:169785118 | TCCAGAAATGTTTAA[A/G]AGGAAATAGGGAAAC | 55892 |
rs58580234 | snp | A/T | | | intron-variant | MYNN | GRCh38.p7 | 3:169782689 | TAAAGTTATAAATAA[A/T]AGAAAAAGGGGACTT | 55892 |
rs61087913 | in-del | -/T | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169772337 | TTTTTTTTTTTTTTT[-/T]CCTTCGCTTGGAAGA | 55892 |
rs61745452 | snp | C/T | 1.64936e-05 | 0.00287168 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | MYNN | GRCh38.p7 | 3:169779257 | ACAAGATATTGTGCA[C/T]ACTGTTACAGTGAAA | 55892 |
rs62293395 | snp | G/T | 0.5 | 0 | intron-variant | ACTRT3 | GRCh38.p7 | 3:169768546 | TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTCGCT | 55892 |
rs62293396 | snp | A/C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169772222 | TACAAAACCCTCTCC[A/C/G]AAGTGGGGTTTCCGT | 55892 |
rs62293397 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | MYNN | GRCh38.p7 | 3:169780257 | TAGAGACTGGGTTTC[A/T]CCATGTTAGCCAGGA | 55892 |
rs71300477 | in-del | -/C | 0.5 | 0 | intron-variant | MYNN | GRCh38.p7 | 3:169785081 | TTCATGATAACACCA[-/C]CCCCCCCCCCCTTTT | 55892 |
rs71306647 | snp | C/T | 0.5 | 0 | utr-variant-5-prime | ACTRT3 | GRCh38.p7 | 3:169769550 | CGCCGCCTCCTGTCT[C/T]TGAGCCGCTCTAGCT | 55892 |
rs71306648 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MYNN | GRCh38.p7 | 3:169772242 | GGGGTTTCCGTAGTG[G/T]AGTGGTTATCACGTT | 55892 |
rs71306649 | snp | A/C | 0.5 | 0 | intron-variant | MYNN | GRCh38.p7 | 3:169776990 | TGCACCCGGCCTTGA[A/C]CAATTAATGTATGAC | 55892 |