SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs794 | snp | A/G | 0.448195 | 0.152377 | intron-variant | EML1 | GRCh38.p7 | 14:99768122 | TGGGATCACTTCTCC[A/G]TGCCCCATCTCTGGG | 2009 |
rs2093 | snp | G/T | 0.491421 | 0.0649309 | intron-variant | EML1 | GRCh38.p7 | 14:99916533 | AGATAAAGGGCACTT[G/T]GCAGGAGTGTTTAGG | 2009 |
rs3328 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99941211 | ATCTGTCACACAATC[A/G]AAATGGATAAGGCCT | 2009 |
rs732786 | snp | G/T | | | intron-variant | EML1 | GRCh38.p7 | 14:99750620 | TATTCAAGGGCACAG[G/T]GGGGGGATCAGGGTG | 2009 |
rs732787 | snp | A/G | 0.499325 | 0.0183582 | intron-variant | EML1 | GRCh38.p7 | 14:99750699 | TGGATGTGGCCTCCT[A/G]AGACAGTCACTCAGG | 2009 |
rs746698 | snp | C/T | 0.376791 | 0.215463 | intron-variant | EML1 | GRCh38.p7 | 14:99886038 | TAAAGTCTCCAGCAA[C/T]TTCTAAACATTTTGA | 2009 |
rs746699 | snp | C/T | 0.097727 | 0.198275 | intron-variant | EML1 | GRCh38.p7 | 14:99886263 | aagacaggcagatca[C/T]ttgaggccaggagtt | 2009 |
rs751324 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | EML1 | GRCh38.p7 | 14:99740679 | GGCGCTTCCTTTACA[G/T]Ttgcctgcattctag | 2009 |
rs751325 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | EML1 | GRCh38.p7 | 14:99740777 | atggggGGTTCGTCA[A/G]TTCTCTCACTGGGTC | 2009 |
rs911914 | snp | A/G | 0.130118 | 0.219732 | intron-variant | EML1 | GRCh38.p7 | 14:99883101 | GTGGATGAAGGGCCC[A/G]GAGCCCCAGCCAAGG | 2009 |
rs911917 | snp | A/C | 0.188316 | 0.242271 | intron-variant | EML1 | GRCh38.p7 | 14:99740652 | ACCGGCCCACACACC[A/C]CGGCCAGCAAAGGCG | 2009 |
rs911918 | snp | C/T | 0.499396 | 0.0173617 | intron-variant | EML1 | GRCh38.p7 | 14:99750753 | AGGCAGGATGGGTTC[C/T]AGGTGGAGTCCAGCT | 2009 |
rs927464 | snp | A/T | 0.0788843 | 0.182262 | intron-variant | EML1 | GRCh38.p7 | 14:99763650 | AATGAGCTTGTGGTC[A/T]TCGTGTTATTGTCCT | 2009 |
rs941837 | snp | A/G | 0.444799 | 0.156695 | intron-variant | EML1 | GRCh38.p7 | 14:99886798 | ACAGATATTCACTGT[A/G]CCTCAGAGCGGGGAT | 2009 |
rs959159 | snp | C/T | 0.130694 | 0.219696 | intron-variant | EML1 | GRCh38.p7 | 14:99876903 | TAGCTTTGCAGAGCC[C/T]TATACAAAAGTTTGG | 2009 |
rs960891 | snp | C/T | 0.447938 | 0.152711 | intron-variant | EML1 | GRCh38.p7 | 14:99748005 | AGGTTCCCTTAGGGC[C/T]GACAGCTGTGACATC | 2009 |
rs971970 | snp | A/T | 0.446118 | 0.155041 | intron-variant | EML1 | GRCh38.p7 | 14:99896080 | AAAAAGGTGAATTAA[A/T]TGTTGATTATTTTTC | 2009 |
rs971971 | snp | A/G | 0.445987 | 0.155207 | intron-variant | EML1 | GRCh38.p7 | 14:99896209 | GAGTACCTGTTTAAT[A/G]CCAAGCCTGGAACAC | 2009 |
rs975252 | snp | C/T | 0.455621 | 0.142197 | intron-variant | EML1 | GRCh38.p7 | 14:99894968 | GCTTCATAAGAGCGG[C/T]TTATTATCAGGAGAA | 2009 |
rs975548 | snp | A/G | 0.461813 | 0.132798 | intron-variant | EML1 | GRCh38.p7 | 14:99877814 | GGAGACCCGGGGTGC[A/G]GCTAGAAATCCTGCA | 2009 |
rs975549 | snp | A/G | 0.130008 | 0.219321 | intron-variant | EML1 | GRCh38.p7 | 14:99877825 | ATGTAGTGGGTGGAG[A/G]CCCGGGGTGCGGCTA | 2009 |
rs976451 | snp | A/C | 0.373397 | 0.217424 | intron-variant | EML1 | GRCh38.p7 | 14:99879076 | TCAGAGGCTATGTTT[A/C]ATATTGATGCTAACA | 2009 |
rs976452 | snp | A/G | 0.372391 | 0.217992 | intron-variant | EML1 | GRCh38.p7 | 14:99879196 | ATTATGATAAGTATC[A/G]GTGAAACTAATAGTA | 2009 |
rs976453 | snp | A/G | 0.465892 | 0.126058 | intron-variant | EML1 | GRCh38.p7 | 14:99879321 | AAATCCAGTTTCTCT[A/G]TGTATTTTTACCTAA | 2009 |
rs1005766 | snp | A/G | 0.25801 | 0.249872 | intron-variant | EML1 | GRCh38.p7 | 14:99893757 | AAACCAGGTCCTTTG[A/G]TCTGCAGTGAAATTT | 2009 |
rs1006927 | snp | A/G | 0.46974 | 0.119223 | intron-variant | EML1 | GRCh38.p7 | 14:99755598 | AGCCAGTCCACAGCC[A/G]GGACAGGAACCAACA | 2009 |
rs1044620 | snp | A/G | 0 | 0 | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99940434 | AAAAATGGGTCACAG[A/G]ATGCCTTTTAAAACA | 2009 |
rs1044622 | snp | A/T | | | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99940458 | TAAAACATTGTATAT[A/T]ATCTTCACTGTTTTC | 2009 |
rs1044623 | snp | A/T | | | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99940476 | TTCACTGTTTTCACC[A/T]TCTAGCTTGCTAAGT | 2009 |
rs1044624 | snp | C/T | | | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99940478 | CACTGTTTTCACCAT[C/T]TAGCTTGCTAAGTCA | 2009 |
rs1044625 | snp | C/G | | | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99940482 | GTTTTCACCATCTAG[C/G]TTGCTAAGTCAAATA | 2009 |
rs1044626 | snp | A/G | | | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99940501 | CTAAGTCAAATATTT[A/G]TGATGATAATGAGGT | 2009 |
rs1044631 | snp | C/T | 0.493247 | 0.0577133 | utr-variant-3-prime | EML1 | GRCh38.p7 | 14:99941044 | GATCTCTCTCGAGCG[C/T]ACCATAAACCTGCAG | 2009 |
rs1044650 | snp | A/G | 0.0198 | 0.0975087 | utr-variant-3-prime, downstream-variant-500B | EML1, LOC102724682 | GRCh38.p7 | 14:99941842 | TAAGATGAGGGAAGG[A/G]AAAGGCATTCATTAT | 2009 |
rs1075899 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | EML1 | GRCh38.p7 | 14:99886682 | GACACGTGGTGACAT[G/T]TGTAAGAAGTCCTGG | 2009 |
rs1077265 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | EML1 | GRCh38.p7 | 14:99886615 | TGCTGTTTGAGCAGA[A/G]ATACTTGCTTTTGAA | 2009 |
rs1077901 | snp | A/T | 0.375399 | 0.216275 | intron-variant | EML1 | GRCh38.p7 | 14:99741350 | TCCCAGCACACGCAC[A/T]TACAAAACGCACCAG | 2009 |
rs1115300 | snp | A/G | 0.288906 | 0.246954 | intron-variant | EML1 | GRCh38.p7 | 14:99837173 | CAGGGCAGCCAAGAC[A/G]ATTGGGGTTCGCAGA | 2009 |
rs1117813 | snp | A/G | 0.463774 | 0.129618 | intron-variant | EML1 | GRCh38.p7 | 14:99836169 | aatccgtgaacatgg[A/G]atatatctccgtttc | 2009 |
rs1191090 | snp | C/T | 0.129664 | 0.219133 | intron-variant | EML1 | GRCh38.p7 | 14:99899020 | CAGACACAAACTTCA[C/T]GGGTTAAAGTCACGA | 2009 |
rs1191091 | snp | A/G | 0.434831 | 0.168337 | intron-variant | EML1 | GRCh38.p7 | 14:99896929 | ATGTAATGTGAATAC[A/G]TATTTTCACAATGAT | 2009 |
rs1191092 | snp | C/T | 0.445196 | 0.1562 | intron-variant | EML1 | GRCh38.p7 | 14:99896768 | TACCTTTTATGTATG[C/T]TTGTGTGCATGTGTG | 2009 |
rs1191093 | snp | C/T | 0.445855 | 0.155373 | intron-variant | EML1 | GRCh38.p7 | 14:99896615 | ATGTAAAAAGTAACC[C/T]GGCAAGATGCCAAAT | 2009 |
rs1191096 | snp | A/G | 0.445987 | 0.155207 | intron-variant | EML1 | GRCh38.p7 | 14:99896019 | TTTTTTCCCCTGGAA[A/G]CTCACTTTTCCAAAC | 2009 |
rs1191097 | snp | A/G | 0.445196 | 0.1562 | intron-variant | EML1 | GRCh38.p7 | 14:99895964 | CTCTGTTTCAAGAAC[A/G]TTAGTTATATGGTTG | 2009 |
rs1191098 | snp | A/G | 0.447421 | 0.153379 | intron-variant | EML1 | GRCh38.p7 | 14:99894518 | ATCAATTAGAATGAC[A/G]GAAGGGTAAAAGTTT | 2009 |
rs1191099 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | EML1 | GRCh38.p7 | 14:99894150 | TTATGTATCTTTTAA[C/T]TGAACAATTCTTTCA | 2009 |
rs1191100 | snp | C/T | 0.424968 | 0.178567 | intron-variant | EML1 | GRCh38.p7 | 14:99891306 | AAAAGAAGTAGCCAG[C/T]TTCAGGGGCCAGCCT | 2009 |
rs1191101 | snp | C/G | 0.129664 | 0.219133 | intron-variant | EML1 | GRCh38.p7 | 14:99890712 | ACCCTGGTGTTCCCC[C/G]CTTCTCTTTCTATTT | 2009 |
rs1191102 | snp | A/G | 0.44638 | 0.154709 | intron-variant | EML1 | GRCh38.p7 | 14:99890295 | CAGGGAAGCTAAGCA[A/G]TGCAAAGCATGAACT | 2009 |
rs1191103 | snp | C/G | 0.129664 | 0.219133 | intron-variant | EML1 | GRCh38.p7 | 14:99888859 | TTTCCCAATTCTACA[C/G]CTCCAGGTGATTTCC | 2009 |
rs1191104 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | EML1 | GRCh38.p7 | 14:99887880 | CTTCTGAACAACTGA[C/T]AGAAAGGCAAACACA | 2009 |
rs1191105 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | EML1 | GRCh38.p7 | 14:99887824 | TTGTTGAGAGGCCAC[A/G]GTGGCTTCAATGTTC | 2009 |
rs1191106 | snp | A/T | 0.445064 | 0.156365 | intron-variant | EML1 | GRCh38.p7 | 14:99887789 | TGTTGACGGGAGCTG[A/T]ATGCAGAAAGTGCAT | 2009 |
rs1191107 | snp | A/G | 0.459118 | 0.137002 | intron-variant | EML1 | GRCh38.p7 | 14:99887300 | AAGACGAACTCCAGC[A/G]CAGTTCTTATTGCTT | 2009 |
rs1191108 | snp | G/T | 0.12932 | 0.218944 | intron-variant | EML1 | GRCh38.p7 | 14:99885601 | TTCAGTAAAAAATGC[G/T]TAAGTCTCATCTTCC | 2009 |
rs1191109 | snp | A/G | 0.459347 | 0.136653 | intron-variant | EML1 | GRCh38.p7 | 14:99885488 | gaaacacccgtgtct[A/G]gcccatgactgCATT | 2009 |
rs1191110 | snp | C/T | 0.375 | 0.216506 | intron-variant | EML1 | GRCh38.p7 | 14:99882664 | gcaattttctttttt[C/T]tttttttttttttta | 2009 |
rs1191111 | snp | C/T | 0.426047 | 0.177503 | intron-variant | EML1 | GRCh38.p7 | 14:99882332 | acatctaacatgaac[C/T]gtgcttctaaataag | 2009 |
rs1191112 | snp | A/G | 0.374 | 0.217081 | intron-variant | EML1 | GRCh38.p7 | 14:99881974 | TCACAAGAAAGACTC[A/G]AATCCAGTGACCATT | 2009 |
rs1191113 | snp | C/T | 0.424968 | 0.178567 | intron-variant | EML1 | GRCh38.p7 | 14:99880631 | TCACAGGACAGCCTG[C/T]AGGAACAATGGACAT | 2009 |
rs1191117 | snp | C/T | 0.40595 | 0.195396 | intron-variant | EML1 | GRCh38.p7 | 14:99878942 | ACTAGAAATCGAAGG[C/T]GCTCAGGTAGAAATT | 2009 |
rs1191118 | snp | A/G | 0.131723 | 0.220251 | intron-variant | EML1 | GRCh38.p7 | 14:99878361 | AAAGACAGGCCTAGC[A/G]ACGGAGATCAAAAAG | 2009 |
rs1191119 | snp | C/T | 0.134802 | 0.221877 | intron-variant | EML1 | GRCh38.p7 | 14:99875950 | TTAACTGGGGAACCC[C/T]TGAGTGGACAGTGCC | 2009 |
rs1191120 | snp | C/T | 0.4628 | 0.13121 | intron-variant | EML1 | GRCh38.p7 | 14:99875645 | GGGCCCTGGGAGATT[C/T]TGCAGCCGCAAGAAG | 2009 |
rs1191121 | snp | C/T | 0.457271 | 0.139781 | intron-variant | EML1 | GRCh38.p7 | 14:99875093 | TGATTGATGACTTGA[C/T]GAATGGTAGGCACTG | 2009 |
rs1191122 | snp | A/T | 0.45843 | 0.138046 | intron-variant | EML1 | GRCh38.p7 | 14:99872358 | TAACACGATGGCTAC[A/T]AAGCATAATTTTTCA | 2009 |
rs1211852 | snp | G/T | 0.425277 | 0.178263 | intron-variant | EML1 | GRCh38.p7 | 14:99881568 | TATGAAAGCAAAACA[G/T]GTAATTACTTTAAAA | 2009 |
rs1467582 | snp | A/C | 0.49928 | 0.018956 | upstream-variant-2KB | EML1 | GRCh38.p7 | 14:99737084 | AGCACCCACACTCTG[A/C]CAGGACCACATGACT | 2009 |
rs1475130 | snp | C/T | 0.380724 | 0.213099 | intron-variant | EML1 | GRCh38.p7 | 14:99758807 | GGACTTTCTGTAAAG[C/T]GCATATTCCTGCCCT | 2009 |
rs1548271 | snp | A/C | 0.398174 | 0.201356 | intron-variant | EML1 | GRCh38.p7 | 14:99756559 | AGATGGTTTGGAGCC[A/C]TATGACAGTCTAAGC | 2009 |
rs1555515 | snp | G/T | | | intron-variant | EML1 | GRCh38.p7 | 14:99786376 | TGGGCAACCACTTTT[G/T]TTCAGAGttcattca | 2009 |
rs1555516 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | EML1 | GRCh38.p7 | 14:99786378 | GGCAACCACTTTTTT[A/C/T]CAGAGttcattcatt | 2009 |
rs1743040 | snp | A/G | 0.412082 | 0.190341 | intron-variant | EML1 | GRCh38.p7 | 14:99884296 | CAGGCTGGGATAAAG[A/G]CAGAAACAGGCGCTG | 2009 |
rs1885594 | snp | A/G | | | intron-variant | EML1 | GRCh38.p7 | 14:99755652 | TCCCATTCCGTGGTC[A/G]CTTGCCCTCCTGGGG | 2009 |
rs1885595 | snp | G/T | 0.110872 | 0.20771 | intron-variant | EML1 | GRCh38.p7 | 14:99759144 | CAAACACTGGGCTGG[G/T]AGTCAGGGTGGGACC | 2009 |
rs1951570 | snp | C/G | 0.126564 | 0.217402 | intron-variant | EML1 | GRCh38.p7 | 14:99840776 | TCTTATCCCTGGATA[C/G]TGAGATAATCACATG | 2009 |
rs1951571 | snp | C/T | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | EML1 | GRCh38.p7 | 14:99848839 | GTGGTGGGGTGCGCC[C/T]GTAGTCCCAGATCCT | 2009 |
rs1951572 | snp | A/G | 0.457037 | 0.140127 | intron-variant, upstream-variant-2KB | EML1 | GRCh38.p7 | 14:99848945 | tgcagcctgggcaac[A/G]gagtaagaccctgtc | 2009 |
rs1951573 | snp | C/T | 0.459004 | 0.137176 | intron-variant | EML1 | GRCh38.p7 | 14:99860044 | CCAAGGCGTGTGCTG[C/T]GTCTTCCAGCTCAGC | 2009 |
rs1951574 | snp | A/C | 0.0689305 | 0.172377 | intron-variant | EML1 | GRCh38.p7 | 14:99880327 | GCAGTAACTCAAAAG[A/C]AGCAGCTAAGACTCG | 2009 |
rs1951577 | snp | A/T | 0.499693 | 0.0123764 | intron-variant | EML1 | GRCh38.p7 | 14:99739093 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGACAGAG | 2009 |
rs1951578 | snp | C/T | 0.232067 | 0.249356 | intron-variant | EML1 | GRCh38.p7 | 14:99746285 | AAAGTGGCACTCTTT[C/T]CCAAAGAAGGGAGCT | 2009 |
rs1951579 | snp | A/G | 0.460252 | 0.135255 | intron-variant | EML1 | GRCh38.p7 | 14:99782443 | GTTTGCTCCCCTCTG[A/G]GCTGTGAGACCCTCG | 2009 |
rs1957506 | snp | A/G | 0.463881 | 0.12944 | intron-variant | EML1 | GRCh38.p7 | 14:99841504 | attggctactgctca[A/G]tttgaatcccaaatc | 2009 |
rs1957507 | snp | C/T | 0.41023 | 0.191902 | intron-variant | EML1 | GRCh38.p7 | 14:99867422 | tatcactttgagtag[C/T]atggagattttagca | 2009 |
rs1957508 | snp | A/G | 0.134802 | 0.221877 | intron-variant | EML1 | GRCh38.p7 | 14:99867463 | TTCCAATCCATAAAC[A/G]TAGGATGTCTTTCTC | 2009 |
rs1957509 | snp | A/G | 0.418007 | 0.185132 | intron-variant | EML1 | GRCh38.p7 | 14:99867525 | tagttctcagtgtat[A/G]agtcttctaactcct | 2009 |
rs1957510 | snp | A/C | 0.418007 | 0.185132 | intron-variant | EML1 | GRCh38.p7 | 14:99868032 | tttatcatgaaaagg[A/C]gttgaattttgtcaa | 2009 |
rs1957511 | snp | C/T | 0.419776 | 0.18351 | intron-variant | EML1 | GRCh38.p7 | 14:99868167 | tccaaatataaatcc[C/T]aatttgtcatggtat | 2009 |
rs1957516 | snp | A/G | 0.376592 | 0.215579 | intron-variant | EML1 | GRCh38.p7 | 14:99742653 | CACTTTCAGGGCTCC[A/G]TGGGGTGACCTGGCA | 2009 |
rs1967759 | snp | A/T | | | intron-variant | EML1 | GRCh38.p7 | 14:99785082 | tttttcaaatggagt[A/T]tcactcttgttgccc | 2009 |
rs1967760 | snp | C/G | 0.460589 | 0.13473 | intron-variant | EML1 | GRCh38.p7 | 14:99788783 | tctcatcattccaaa[C/G]ggaaactttgcgccc | 2009 |
rs1972482 | snp | G/T | 0.396727 | 0.202413 | intron-variant | EML1 | GRCh38.p7 | 14:99756637 | AAACCTTTGGCCCAG[G/T]GGTTCTCAAACGCTG | 2009 |
rs1972483 | snp | C/T | 0.439918 | 0.162576 | intron-variant | EML1 | GRCh38.p7 | 14:99756771 | TTCCCGTGCCCCCAG[C/T]GTTTGAAGTTCAGTG | 2009 |
rs1998385 | snp | A/T | 0.360421 | 0.224293 | intron-variant | EML1 | GRCh38.p7 | 14:99895549 | CCACATTGGCAAAAA[A/T]GTTTTTAAACCCAAA | 2009 |
rs2015968 | snp | A/T | 0.494855 | 0.0504572 | intron-variant | EML1 | GRCh38.p7 | 14:99755503 | GCACTAGGCACTTGG[A/T]AGCCTCTCTTCTGGA | 2009 |
rs2057397 | snp | A/G | 0.377977 | 0.21476 | intron-variant | EML1 | GRCh38.p7 | 14:99892529 | CCTCTTCCCACTAGC[A/G]CCTTTGGGTTTGGTG | 2009 |
rs2093357 | snp | C/T | 0.493154 | 0.0581045 | intron-variant | EML1 | GRCh38.p7 | 14:99900349 | ATACAAAAAATTAGC[C/T]GGGCGTGGTAGTGCA | 2009 |
rs2145859 | snp | C/T | 0.192755 | 0.243358 | intron-variant | EML1 | GRCh38.p7 | 14:99910378 | TCTCTTACAACATTA[C/T]CAAAAACCATTGGTT | 2009 |