SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11171 | snp | A/G | 0.109342 | 0.206677 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888489 | CACAATGGCCCTTGG[A/G]TCTCCACGAACCATC | 402682 |
rs1799806 | snp | C/G | 0.498544 | 0.0269388 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891037 | ATGGGGAGGCTGCTC[C/G]GAGGCCCGGCCTCCC | 402682 |
rs2251631 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889741 | aggggaggggagggg[A/C]ggggcggggcggggC | 402682 |
rs2396755 | snp | C/T | 0.138886 | 0.22395 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889899 | CTCGGAGCTCGCCTG[C/T]TTCTTGCCCTCCAGC | 402682 |
rs2720392 | snp | G/T | 0.474959 | 0.109056 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888414 | GGGAGTCTGCAGGCG[G/T]CAACAAAGCTTGGGC | 402682 |
rs2733917 | snp | A/T | 0 | 0 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888537 | TGCCCCAGACGATGT[A/T]GATTTCTTTTGAGCC | 402682 |
rs2733918 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889514 | GGGCGGTGGGCGGGA[A/G]CGGATGTCCCATGCC | 402682 |
rs2733919 | snp | A/G/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889519 | GTGGGCGGGAACGGA[A/G/T]GTCCCATGCCAGGCA | 402682 |
rs2733920 | snp | G/T | | | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889526 | GGAACGGATGTCCCA[G/T]GCCAGGCACAGCGTC | 402682 |
rs3087504 | snp | C/T | 0.499999 | 0.000668008 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888467 | TCCTGTACCTCTCAC[C/T]TCACAGGATGGTTCG | 402682 |
rs3178268 | snp | A/C/T | 1.65449e-05 | 0.00287614 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888659 | AATAAAAGCACTTCC[A/C/T]CAGGGCTCCTGACTC | 402682 |
rs4996164 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889753 | CCCGCCCCTCCCCTC[C/T]CCTCCCCTCCCCTCC | 402682 |
rs11974682 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891698 | GATCCAGGTAAACTG[A/G]TGTGTGTGTGAGAGA | 402682 |
rs12666989 | snp | C/G | 0.263392 | 0.249641 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889133 | AGTAAAGCCTCTCCA[C/G]CTCCCCGTGCAGCCC | 402682 |
rs13241786 | snp | G/T | 0.4773 | 0.10409 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889035 | TTCCGTGCCTGACCC[G/T]ACGCAGACTCCCAGC | 402682 |
rs17228602 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890786 | CAAAGGCGTGGGGGT[C/T]CCTGAGAAGGGTGGG | 402682 |
rs17228609 | snp | C/T | 0.0123036 | 0.0774623 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890127 | GCAGAGTCTGGGGCT[C/T]GTCTGTGTTATAGCC | 402682 |
rs17228616 | snp | G/T | 0.16976 | 0.236773 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890100 | GGGGACGTCGGGGTG[G/T]GGTGGGGATGGGCAG | 402682 |
rs17235010 | snp | A/G | 0.00210837 | 0.0323997 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890909 | CTCCTCTAATGAGTG[A/G]TCGGACCGTGGGGAA | 402682 |
rs17880700 | snp | A/C | 0.0821764 | 0.185298 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889696 | TGGGAGCTCCTCGGT[A/C]GGTGCCGGTCGGTGG | 402682 |
rs17882992 | snp | C/T | 0.00797827 | 0.0626537 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888395 | CAAAGCTTGGGCGTC[C/T]GCCCTCCTCACCTGT | 402682 |
rs17883268 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890549 | CTCCTCTCTCCTTCC[C/T]GCTGTCCTTCTCCGG | 402682 |
rs17885823 | snp | C/T | 0.0123036 | 0.0774623 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889680 | GGTGCCGGTCGGTGG[C/T]TGCCTATTGCGGCCT | 402682 |
rs17886048 | snp | A/G | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891617 | GATGTTTGTAGACAT[A/G]GGACCCGTCCTGGTT | 402682 |
rs17886712 | snp | A/G | 0.0532157 | 0.154195 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891496 | AGCGCTTGAGGAAGG[A/G]AAGACCCCAATGACC | 402682 |
rs17886728 | snp | A/C | 0.0147827 | 0.0846925 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891017 | CCCGGCCTCCCCCTG[A/C]CCCTCCTCCTCCTCC | 402682 |
rs28379036 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889763 | CCCTCCCCTCCCCTC[C/T]CCTCCCCTCCCCTCT | 402682 |
rs60031054 | in-del | -/GCCCCTCCCCTCCCCTCCCCTCCCC | 0 | 0 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889741 | GCCCCGCCCCGCCCC[-/GCCCCTCCCCTCCCCTCCCCTCCCC]TCCCCTCCCCTCTCC | 402682 |
rs62482512 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889758 | CCCTCCCCTCCCCTC[C/T]CCTCCCCTCCCCTCC | 402682 |
rs73396648 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888761 | TATTGATGTCAAAAG[C/T]GCCAGGCTTTGCAGG | 402682 |
rs76450656 | snp | C/T | 0.00828201 | 0.0638155 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888398 | GGTGAGGAGGGCAGA[C/T]GCCCAAGCTTTGTTG | 402682 |
rs78082054 | snp | A/T | 0 | 0 | intron-variant, splice-donor-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888385 | GCGTCTGCCCTCCTC[A/T]CCTGTTGCGAGGTTT | 402682 |
rs78317606 | in-del | -/A | | | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888924 | GGGTCAAAGGCTGCA[-/A]CTCACCTCTTGCCAG | 402682 |
rs78663731 | snp | A/C/G | 0.000105909 | 0.00727628 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888803 | GAGGTACATAGGTGC[A/C/G]TGTCTGGGACCCGAG | 402682 |
rs80156244 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890559 | ACAGCAGGAAGGAGA[A/G]AGGAGGAGAAAAGAA | 402682 |
rs80265517 | snp | G/T | | | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888386 | AACCTCGCAACAGGT[G/T]AGGAGGGCAGACGCC | 402682 |
rs111902319 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889904 | AGCTCGCCTGTTTCT[C/T]GCCCTCCAGCCCCGC | 402682 |
rs112259347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891406 | CCCAACTCCACGGGA[C/T]CCCGGACTCTTCAGC | 402682 |
rs112427842 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889674 | CACCGCAGGCCGCAA[G/T]AGGCAGCCACCGACC | 402682 |
rs113616334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890423 | GGGTTGAAGGGGGGG[C/T]ATGAGTGCAGGGAGG | 402682 |
rs114922826 | snp | A/C/G/T | 0.000649095 | 0.0180042 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888628 | GAGAATTTTTTGTAC[A/C/G/T]ATCAGCCTTACTGCT | 402682 |
rs115089874 | snp | A/G | 0.000814001 | 0.0201578 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891157 | AGCCGCTGCCCGCTG[A/G]CCCCTGCATACCGGT | 402682 |
rs137910416 | snp | G/T | 0.0284598 | 0.115844 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888664 | AAGCACTTCCACAGG[G/T]CTCCTGACTCTCGTG | 402682 |
rs139519950 | snp | C/G/T | 1.65674e-05 | 0.00287809 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888376 | TATCCTGGGAAACCT[C/G/T]GCAACAGGTGAGGAG | 402682 |
rs139696379 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891486 | CAATGTGCGCGGTCA[C/T]TGGGGTCTTCCCTTC | 402682 |
rs140228675 | snp | C/T | 3.31208e-05 | 0.00406931 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888417 | CAAGCTTTGTTGCCG[C/T]CTGCAGACTCCCTTT | 402682 |
rs140501227 | snp | C/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888977 | GTTCACTGGGGCTTT[C/T]TGGAGTGCCCCAGTA | 402682 |
rs141166290 | snp | G/T | 0.00194027 | 0.0310865 | stop-lost, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888843 | TCTGTAACTTCGTCC[G/T]CAGTCCAAGGTGCGC | 402682 |
rs142627875 | snp | C/G | 0.000132177 | 0.0081284 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888341 | GAGGGAACTATGATG[C/G]CTTCCGAGGCCAGGG | 402682 |
rs142793647 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889761 | TCCCCTCCCCTCCCC[G/T]CCCCTCCCCTCCCCT | 402682 |
rs142801971 | snp | C/T | 4.96792e-05 | 0.00498368 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889043 | CTGACCCTACGCAGA[C/T]TCCCAGCAAGGCCTT | 402682 |
rs143351272 | snp | G/T | 0.000527644 | 0.016234 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888913 | TAGAAGGAGTTGGGG[G/T]CAAAGGCTGCACTCA | 402682 |
rs144293839 | snp | G/T | 0.00551091 | 0.0522023 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890213 | GGGGGTCCCGCCGGG[G/T]TCACAGGTCTGAGCA | 402682 |
rs145643348 | snp | C/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888856 | CCTCAGTCCAAGGTG[C/T]GCTGCTGCTGTTGGG | 402682 |
rs145741868 | snp | C/G/T | 0.000153988 | 0.00877328 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888978 | TTCACTGGGGCTTTT[C/G/T]GGAGTGCCCCAGTAG | 402682 |
rs146266307 | snp | C/G | 0.000333195 | 0.012903 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889066 | AAGGCCTTGGACCTG[C/G]CATCTGCGTCCCCCC | 402682 |
rs146285121 | snp | C/T | 1.65446e-05 | 0.00287612 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888281 | TCCGCCCTGCAGTCC[C/T]CACAGGAGGCCCTCC | 402682 |
rs147386700 | snp | A/G | 1.98065e-05 | 0.00314688 | synonymous-codon, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890268 | GAACTGGTTCTTCCA[A/G]TGCACCATGTAGGAG | 402682 |
rs147414076 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889792 | CTCCTCCCCTCCGCC[A/G]TGCCAGCTAGCCTGC | 402682 |
rs147752098 | snp | A/G | 1.65173e-05 | 0.00287374 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888899 | TCAAGCACAGGTTGT[A/G]GAAGGAGTTGGGGTC | 402682 |
rs147770073 | snp | C/T | 0.00121483 | 0.0246159 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888842 | TTCTGTAACTTCGTC[C/T]TCAGTCCAAGGTGCG | 402682 |
rs148315224 | snp | C/T | 3.29598e-05 | 0.00405941 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888929 | CAAAGGCTGCACTCA[C/T]CTCTTGCCAGCCCAC | 402682 |
rs148451475 | snp | A/G/T | 6.6036e-05 | 0.00574575 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888312 | ATACCCCCATGCCCC[A/G/T]TATGGTGCTGGTCGA | 402682 |
rs148676511 | snp | A/G | 0.00020589 | 0.0101441 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889200 | CCCTCCGAAGTGAGC[A/G]AGGCAGAGGCTGGCC | 402682 |
rs149184662 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888911 | TGTAGAAGGAGTTGG[A/G]GTCAAAGGCTGCACT | 402682 |
rs149499170 | snp | A/C/G/T | 0.00292541 | 0.0381352 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889081 | GCATCTGCGTCCCCC[A/C/G/T]CAACCATGACTGGGC | 402682 |
rs149782561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891679 | ATTTCATTGTCCTCT[C/T]CTCGATCCAGGTAAA | 402682 |
rs150287642 | snp | A/T | 0.0109821 | 0.0732833 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888465 | CATCCTGTACCTCTC[A/T]CCTCACAGGATGGTT | 402682 |
rs150948431 | snp | G/T | 8.27959e-05 | 0.00643359 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888368 | AGGGAGGTTATCCTG[G/T]GAAACCTCGCAACAG | 402682 |
rs180979674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888448 | TGGGAGCCCTCAGCT[C/G]TCATCCTGTACCTCT | 402682 |
rs185805997 | snp | A/G | 1.80465e-05 | 0.00300382 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888614 | TCCTATGAAGCTCTG[A/G]GAATTTTTTGTACGA | 402682 |
rs187867886 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891494 | GCGGTCATTGGGGTC[A/T]TCCCTTCCTCAAGCG | 402682 |
rs190663480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890676 | TGGGGGGTGCTACCC[C/T]GTCCGGGGCCTCCCA | 402682 |
rs191455018 | snp | G/T | | | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889352 | AGCACAGCGTCTGCA[G/T]AGTGCGGTAGCCGCA | 402682 |
rs199673430 | snp | C/T | 0.000635784 | 0.0178182 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888802 | GGAGGTACATAGGTG[C/T]GTGTCTGGGACCCGA | 402682 |
rs199815193 | snp | A/G | 0.000798403 | 0.0199641 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888850 | CTTCGTCCTCAGTCC[A/G]AGGTGCGCTGCTGCT | 402682 |
rs199826303 | snp | A/C/G | 0.000169678 | 0.00920926 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890991 | GGAGAGGAAGAGGAG[A/C/G]AGAAGCTGGTGGAGG | 402682 |
rs199927605 | snp | A/G | 1.79319e-05 | 0.00299427 | missense | UFSP1 | GRCh38.p7 | 7:100889183 | CAGAGGCGTCCCTGG[A/G]GCCCTCCGAAGTGAG | 402682 |
rs200182652 | in-del | -/CCCCTCCCCTCCCCTCCCCT | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889742 | CCCCGCCCCGCCCCG[-/CCCCTCCCCTCCCCTCCCCT]CCCCTCCCCTCCCCT | 402682 |
rs200218274 | snp | C/T | 0.00436448 | 0.0465101 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888415 | CCCAAGCTTTGTTGC[C/T]GCCTGCAGACTCCCT | 402682 |
rs200431197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890979 | CCGCCGGAGGTGGGA[A/G]AGGAAGAGGAGGAGA | 402682 |
rs200680733 | snp | C/T | 3.30376e-05 | 0.0040642 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888293 | TCCCCACAGGAGGCC[C/T]TCCATACCCCCATGC | 402682 |
rs200758558 | in-del | -/CTT | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891519 | CAAGCGCTCCGTCTC[-/CTT]CCGTTTCCCTCAGCT | 402682 |
rs200859645 | snp | A/G | 6.671e-05 | 0.00577499 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888878 | GCTGTTGGGAGCTAA[A/G]GCTGGTCAAGCACAG | 402682 |
rs200894711 | snp | C/G | 1.75619e-05 | 0.00296321 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888824 | GGGACCCGAGAATCT[C/G]AGTTCTGTAACTTCG | 402682 |
rs201307521 | snp | A/C/G | 3.48598e-05 | 0.00417479 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889157 | GCAGCCCCACTCCCC[A/C/G]GGGTACGTGGCAGAG | 402682 |
rs201344558 | snp | A/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891285 | TACTGCTGAGCCCCC[A/G]CCGTGTACGGGGGCC | 402682 |
rs201488830 | snp | C/T | 1.66056e-05 | 0.00288141 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889056 | GACTCCCAGCAAGGC[C/T]TTGGACCTGGCATCT | 402682 |
rs201836239 | snp | C/T | 0.00420629 | 0.0456668 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890209 | ACATGGGGGTCCCGC[C/T]GGGGTCACAGGTCTG | 402682 |
rs202030567 | snp | A/G | 0.00439459 | 0.0466688 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888603 | GTACTACCTTGTCCT[A/G]TGAAGCTCTGAGAAT | 402682 |
rs368422793 | snp | C/T | 5.29469e-05 | 0.00514496 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888807 | TACATAGGTGCGTGT[C/T]TGGGACCCGAGAATC | 402682 |
rs368510156 | snp | C/T | 3.93352e-05 | 0.00443464 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891363 | GAAGGGAAGGCTCAG[C/T]CCAGACGGGCAGTGG | 402682 |
rs368720237 | snp | A/C/G | 8.51312e-05 | 0.00652377 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888595 | CCATACTTGTACTAC[A/C/G]TTGTCCTATGAAGCT | 402682 |
rs368786443 | snp | C/T | | | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888531 | CCTGGATGCCCCAGA[C/T]GATGTTGATTTCTTT | 402682 |
rs369098327 | snp | A/G | 1.83239e-05 | 0.00302682 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889194 | CTGGGGCCCTCCGAA[A/G]TGAGCGAGGCAGAGG | 402682 |
rs369210024 | snp | C/T | 9.95421e-05 | 0.00705416 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888401 | GAGGAGGGCAGACGC[C/T]CAAGCTTTGTTGCCG | 402682 |
rs369963076 | snp | G/T | 0.000153988 | 0.00877328 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888359 | TCCGAGGCCAGGGAG[G/T]TTATCCTGGGAAACC | 402682 |
rs370027511 | snp | A/C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889896 | CGCCTCGGAGCTCGC[A/C/G]TGTTTCTTGCCCTCC | 402682 |
rs370031049 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890107 | TCGGGGTGGGGTGGG[A/G]ATGGGCAGAGTCTGG | 402682 |
rs370080677 | snp | C/T | 0.000889797 | 0.0210738 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889020 | TACCAGGACATAGGC[C/T]TCCGTGCCTGACCCT | 402682 |