| 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 |
| rs370133260 | snp | C/G | | | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889136 | AAAGCCTCTCCAGCT[C/G]CCCGTGCAGCCCCAC | 402682 |
| rs370307936 | snp | A/G | 3.29527e-05 | 0.00405898 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888507 | AAGGGCCATTGTGGA[A/G]TATCGGGACCTGGAT | 402682 |
| rs370551781 | snp | A/G/T | 2.6123e-05 | 0.00361397 | synonymous-codon, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890328 | GCGCTCCGCCTCGTC[A/G/T]AGCGTGTCTGCGGCC | 402682 |
| rs371124764 | snp | A/G | 0.000661967 | 0.0181809 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888424 | TGTTGCCGCCTGCAG[A/G]CTCCCTTTTGGGAGC | 402682 |
| rs372235144 | snp | A/G | 1.97058e-05 | 0.00313887 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891366 | GGGAAGGCTCAGTCC[A/G]GACGGGCAGTGGGAG | 402682 |
| rs372681909 | snp | C/T | 4.50126e-05 | 0.00474387 | missense | UFSP1 | GRCh38.p7 | 7:100889237 | CAGCCGATCCAGTCC[C/T]GGGAGCCCCGGAAGC | 402682 |
| rs372960530 | snp | A/C/G | 3.29953e-05 | 0.00406162 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888909 | GTTGTAGAAGGAGTT[A/C/G]GGGTCAAAGGCTGCA | 402682 |
| rs373699519 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888558 | CTTTTGAGCCGTCCC[C/T]CGTTCCTCAGTCCTG | 402682 |
| rs373801320 | snp | C/T | 0.000392498 | 0.0140034 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891311 | GGGCCATTGTGGGGC[C/T]TTGGGGTCTCGGGGC | 402682 |
| rs374208818 | snp | A/C | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890230 | CACAGGTCTGAGCAG[A/C]GATCCTGCTTGCTGT | 402682 |
| rs374570379 | snp | C/T | 8.24287e-05 | 0.00641931 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889023 | CAGGACATAGGCTTC[C/T]GTGCCTGACCCTACG | 402682 |
| rs374827711 | snp | C/T | 0.000159579 | 0.00893106 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890932 | TAGAGGAGGGGCCCC[C/T]GTGGCCGTAGGGGAA | 402682 |
| rs375074078 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888992 | TTGGAGTGCCCCAGT[A/G]GTGAGGGTCCAATAC | 402682 |
| rs375100557 | snp | G/T | 1.97272e-05 | 0.00314057 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891367 | GGAAGGCTCAGTCCA[G/T]ACGGGCAGTGGGAGG | 402682 |
| rs375151616 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890419 | GGGCGGGTTGAAGGG[C/G]GGGTATGAGTGCAGG | 402682 |
| rs375567360 | snp | C/T | 8.26644e-05 | 0.00642848 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888571 | CCCCGTTCCTCAGTC[C/T]TGTATCATCCATACT | 402682 |
| rs375619969 | snp | A/G/T | 3.31083e-05 | 0.00406857 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888426 | TTGCCGCCTGCAGAC[A/G/T]CCCTTTTGGGAGCCC | 402682 |
| rs375981378 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889878 | TGGCCTTTGCCTTGC[A/G]CCCGCCTCGGAGCTC | 402682 |
| rs376057159 | snp | A/G | 1.75906e-05 | 0.00296564 | missense | UFSP1 | GRCh38.p7 | 7:100889169 | CCCGGGGTACGTGGC[A/G]GAGGCGTCCCTGGGG | 402682 |
| rs376557679 | snp | C/T | | | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888263 | CTGTCATAGCTGGTG[C/T]TGTCCGCCCTGCAGT | 402682 |
| rs376982742 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888429 | CCGCCTGCAGACTCC[C/T]TTTTGGGAGCCCTCA | 402682 |
| rs377312174 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889746 | GCCCCGCCCCGCCCC[C/T]CCCCTCCCCTCCCCT | 402682 |
| rs377417829 | snp | A/G | 4.97014e-05 | 0.0049848 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888416 | CCAAGCTTTGTTGCC[A/G]CCTGCAGACTCCCTT | 402682 |
| rs377635698 | snp | A/G | 0.000165478 | 0.00909459 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889038 | CGTGCCTGACCCTAC[A/G]CAGACTCCCAGCAAG | 402682 |
| rs377683875 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888434 | TGCAGACTCCCTTTT[A/G]GGAGCCCTCAGCTCT | 402682 |
| rs530368519 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889407 | GTCGCAGCCGTAGTG[A/G]TAGTAGAGGTAGTGG | 402682 |
| rs531065307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890926 | ACTCATTAGAGGAGG[A/G]GCCCCTGTGGCCGTA | 402682 |
| rs531395501 | snp | A/G | 0.000107328 | 0.00732478 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889257 | GCCCCGGAAGCCGGG[A/G]GGCTTGTCGCCCATG | 402682 |
| rs532178082 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889365 | CAGAGTGCGGTAGCC[C/G]CAGCCCCAGCCGCGG | 402682 |
| rs536726911 | snp | A/G | 3.31735e-05 | 0.00407255 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888405 | AGGGCAGACGCCCAA[A/G]CTTTGTTGCCGCCTG | 402682 |
| rs536905617 | snp | A/C/G | 0.000221383 | 0.0105191 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891147 | CCCTCCTCCCAGCCG[A/C/G]TGCCCGCTGGCCCCT | 402682 |
| rs537227711 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889586 | CCAACACTTCCTTTC[A/G]GCTCCGGGTCTTGGG | 402682 |
| rs537404942 | snp | A/C | | | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889502 | TCAGCGGCTCCAGGG[A/C]GGTGGGCGGGAGCGG | 402682 |
| rs537594042 | snp | A/G | 1.69123e-05 | 0.0029079 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889110 | GCCCCCACCCCCTGC[A/G]AAGTGCGAGTAAAGC | 402682 |
| rs539523870 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, cds-indel, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890624 | GGAGGTTGGGGGAAA[-/AAG]AAGAGACAGAAATGG | 402682 |
| rs539687404 | snp | A/C | | | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888285 | CCCTGCAGTCCCCAC[A/C]GGAGGCCCTCCATAC | 402682 |
| rs540772563 | in-del | -/ATAAA | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890733 | CCAAAAGATAATTTT[-/ATAAA]AGAATACTGGCTTTT | 402682 |
| rs541013984 | snp | C/T | 0.000121089 | 0.00778011 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889146 | CAGCTCCCCGTGCAG[C/T]CCCACTCCCCGGGGT | 402682 |
| rs541130846 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888790 | GGGACACCAGTGGGA[G/T]GTACATAGGTGCGTG | 402682 |
| rs541165973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890742 | AATTTTATAAAAGAA[A/T]ACTGGCTTTTCCATT | 402682 |
| rs542379557 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888762 | ATTGATGTCAAAAGC[A/G]CCAGGCTTTGCAGGG | 402682 |
| rs542418236 | snp | C/T | 4.22619e-05 | 0.00459664 | missense | UFSP1 | GRCh38.p7 | 7:100889217 | GGCAGAGGCTGGCCT[C/T]CACGCAGCCGATCCA | 402682 |
| rs543183889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888227 | AATTGAGGACATAGT[C/T]TTGCAACTCAACACT | 402682 |
| rs543235565 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889777 | CCCCTCCCCTCCCCT[C/T]TCCTCCCCTCCGCCG | 402682 |
| rs543549250 | snp | A/G | 8.1937e-05 | 0.00640014 | missense | UFSP1 | GRCh38.p7 | 7:100889259 | CCCGGAAGCCGGGGG[A/G]CTTGTCGCCCATGTC | 402682 |
| rs544951161 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888732 | GAGGTGTTGCTCAGC[C/T]CTGCCACTTTTATTA | 402682 |
| rs546387821 | snp | A/G | 0.000611013 | 0.0174681 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890927 | CTCATTAGAGGAGGG[A/G]CCCCTGTGGCCGTAG | 402682 |
| rs546680704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890508 | ATGTGCGAAAGACGA[C/G]AGGGAGGATGAGGGC | 402682 |
| rs547380547 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889366 | AGAGTGCGGTAGCCG[C/T]AGCCCCAGCCGCGGT | 402682 |
| rs548137293 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888963 | CCCAGCAGCCTGTAG[C/T]TCACTGGGGCTTTTT | 402682 |
| rs548893824 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889936 | CCTGCATAGACTCGG[C/T]CCCCGTGATTCCGGC | 402682 |
| rs548969597 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890017 | ACAGTTTATTGGCAG[C/G]CCAGAGGGGCGAAGG | 402682 |
| rs550669871 | snp | C/T | 0.000150614 | 0.00867665 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891110 | GGAGAAGAGAGGGGT[C/T]ACACCTGGCGGGCTC | 402682 |
| rs551006164 | snp | C/T | | | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888986 | GGCTTTTTGGAGTGC[C/T]CCAGTAGTGAGGGTC | 402682 |
| rs552677066 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889639 | GCAGACTGGGGACGC[C/G]CTCCCCGGGCCTCGT | 402682 |
| rs552902607 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889678 | GCAGGCCGCAATAGG[A/C]AGCCACCGACCGGCA | 402682 |
| rs552985032 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891658 | ACAACACCCATCCAA[C/T]GCTAGATTTCATTGT | 402682 |
| rs552999482 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891469 | CCTCCCACCACTTTC[C/T]CCAATGTGCGCGGTC | 402682 |
| rs553083565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890775 | CATTCAAACAACAAA[A/G]GCGTGGGGGTCCCTG | 402682 |
| rs554495533 | snp | A/C/T | 8.24105e-05 | 0.0064187 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888552 | TGATTTCTTTTGAGC[A/C/T]GTCCCCCGTTCCTCA | 402682 |
| rs554563565 | snp | C/T | 0.0349115 | 0.127424 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889768 | CCCTCCCCTCCCCTC[C/T]CCTCCCCTCTCCTCC | 402682 |
| rs554881705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890641 | GAAGAGACAGAAATG[G/T]TTGACCGTTATAGCC | 402682 |
| rs555030402 | snp | C/G | | | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889459 | ACAGGGCCGCGGCTC[C/G]GCGGGGACAGGCCCA | 402682 |
| rs555115495 | snp | A/C/G | 3.3309e-05 | 0.00408089 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889065 | CAAGGCCTTGGACCT[A/C/G]GCATCTGCGTCCCCC | 402682 |
| rs556503915 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890663 | GTTATAGCCCCAATG[C/G]GGGGTGCTACCCCGT | 402682 |
| rs556644803 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891530 | TCTCCTTCCGTTTCC[C/G]TCAGCTTTTCTGTTC | 402682 |
| rs558736410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890721 | CAGGCTCAGGTTCCA[A/G]AAGATAATTTTATAA | 402682 |
| rs558780750 | snp | C/G/T | 5.08361e-05 | 0.00504142 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889116 | ACCCCCTGCGAAGTG[C/G/T]GAGTAAAGCCTCTCC | 402682 |
| rs558863690 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888668 | ACTTCCACAGGGCTC[C/T]TGACTCTCGTGTGTT | 402682 |
| rs559996179 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888744 | AGCCCTGCCACTTTT[A/T]TTATTGATGTCAAAA | 402682 |
| rs560107719 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889401 | CAGGCCGTCGCAGCC[A/G]TAGTGGTAGTAGAGG | 402682 |
| rs561097507 | snp | A/G | 2.12181e-05 | 0.00325709 | missense | UFSP1 | GRCh38.p7 | 7:100889223 | GGCTGGCCTCCACGC[A/G]GCCGATCCAGTCCCG | 402682 |
| rs561364526 | snp | C/T | 1.6563e-05 | 0.00287771 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888275 | GTGCTGTCCGCCCTG[C/T]AGTCCCCACAGGAGG | 402682 |
| rs564034472 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890849 | GTGAGTCTCTCGGTT[G/T]GAGGAGGAAGGGAGC | 402682 |
| rs564380667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890953 | CGTAGGGGAAGAGGC[C/G]GTGTTCACAGCCGCC | 402682 |
| rs564416739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891675 | CTAGATTTCATTGTC[C/T]TCTTCTCGATCCAGG | 402682 |
| rs564807142 | snp | C/T | 0.000149131 | 0.00863385 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889313 | CCAGTCCAGGTACGC[C/T]CGCGGGCTGGCCCTC | 402682 |
| rs565005287 | snp | A/C | 0.00199481 | 0.0315187 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889838 | CGCAGGCGCGAGCTC[A/C]GCCCGGCAGGGCAGG | 402682 |
| rs565882988 | snp | C/G/T | 0.000128193 | 0.00800521 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888676 | AGGGCTCCTGACTCT[C/G/T]GTGTGTTACATAACT | 402682 |
| rs567340203 | snp | G/T | 0.000132192 | 0.00812887 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888447 | TTGGGAGCCCTCAGC[G/T]CTCATCCTGTACCTC | 402682 |
| rs568161125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890548 | GCCGGAGAAGGACAG[C/G]AGGAAGGAGAGAGGA | 402682 |
| rs568447618 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890084 | AGGACCGGGAGCCCC[A/G]GGGGACGTCGGGGTG | 402682 |
| rs569933984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891114 | AAGAGAGGGGTTACA[C/T]CTGGCGGGCTCCCAC | 402682 |
| rs570086495 | snp | A/G | | | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889501 | CTCAGCGGCTCCAGG[A/G]CGGTGGGCGGGAGCG | 402682 |
| rs570279154 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889568 | GCGGAGCGACCTCAG[A/G]CTCCAACACTTCCTT | 402682 |
| rs570580442 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889646 | GGGGACGCGCTCCCC[A/G]GGCCTCGTTGATCAC | 402682 |
| rs574013626 | snp | A/G | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891370 | AGGCTCAGTCCAGAC[A/G]GGCAGTGGGAGGAGG | 402682 |
| rs574521787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890778 | TCAAACAACAAAGGC[A/G]TGGGGGTCCCTGAGA | 402682 |
| rs575169201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891549 | GCTTTTCTGTTCCAT[C/T]TTTGTTTCTCTCACT | 402682 |
| rs576212907 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889773 | CCCTCCCCTCCCCTC[C/T]CCTCTCCTCCCCTCC | 402682 |
| rs576444375 | snp | G/T | 9.82154e-05 | 0.007007 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888636 | TTTGTACGATCAGCC[G/T]TACTGCTAATAAAAG | 402682 |
| rs576981026 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889875 | GGTTGGCCTTTGCCT[G/T]GCGCCCGCCTCGGAG | 402682 |
| rs577019712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890739 | GATAATTTTATAAAA[A/G]AATACTGGCTTTTCC | 402682 |
| rs745310637 | snp | A/G | 1.72018e-05 | 0.00293268 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888851 | TTCGTCCTCAGTCCA[A/G]GGTGCGCTGCTGCTG | 402682 |
| rs745350659 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890171 | AATAGTATATACAGC[C/T]AGGGGGCCGGGCGGA | 402682 |
| rs745396062 | snp | A/G | 5.49254e-05 | 0.0052402 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891030 | GGGCAGGGGGAGGCC[A/G]GGCCTCGGAGCAGCC | 402682 |
| rs745436561 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891152 | CTCCCAGCCGCTGCC[C/T]GCTGGCCCCTGCATA | 402682 |
| rs745588964 | snp | C/G | 3.94337e-05 | 0.00444019 | missense | UFSP1 | GRCh38.p7 | 7:100889208 | AGTGAGCGAGGCAGA[C/G]GCTGGCCTCCACGCA | 402682 |
| rs745885928 | snp | G/T | 2.5696e-05 | 0.00358432 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891200 | TTTGGGGAGGAAGCG[G/T]TTCCAGAAGGCGCAG | 402682 |
| rs746069373 | snp | A/G | 4.99488e-05 | 0.00499719 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888582 | AGTCCTGTATCATCC[A/G]TACTTGTACTACCTT | 402682 |
| rs746095724 | snp | A/G | | | intron-variant, splice-donor-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888384 | GAAACCTCGCAACAG[A/G]TGAGGAGGGCAGACG | 402682 |
| rs746139466 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890374 | GCGGGAGGGGAGGAC[C/G]GCACGAGGAAGGTCG | 402682 |
| rs746174336 | snp | C/T | 1.67301e-05 | 0.00289219 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888228 | ATTGAGGACATAGTT[C/T]TGCAACTCAACACTG | 402682 |
| rs746335644 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889011 | AGGGTCCAATACCAG[A/G]ACATAGGCTTCCGTG | 402682 |
| rs746451069 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888932 | AGGCTGCACTCACCT[C/T]TTGCCAGCCCACCCA | 402682 |
| rs746638472 | snp | C/G | 1.6486e-05 | 0.00287102 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888919 | GAGTTGGGGTCAAAG[C/G]CTGCACTCACCTCTT | 402682 |
| rs746667731 | in-del | -/T | 1.67337e-05 | 0.00289251 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888226 | GAATTGAGGACATAG[-/T]TTTGCAACTCAACAC | 402682 |
| rs746726489 | snp | A/T | 3.3861e-05 | 0.00411453 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888862 | TCCAAGGTGCGCTGC[A/T]GCTGTTGGGAGCTAA | 402682 |
| rs746847406 | snp | C/T | 2.82538e-05 | 0.00375847 | missense | UFSP1 | GRCh38.p7 | 7:100889261 | CGGAAGCCGGGGGGC[C/T]TGTCGCCCATGTCCT | 402682 |
| rs746962787 | snp | A/T | 0.000211189 | 0.0102737 | missense | UFSP1 | GRCh38.p7 | 7:100889216 | AGGCAGAGGCTGGCC[A/T]CCACGCAGCCGATCC | 402682 |
| rs747037374 | snp | C/T | 1.97463e-05 | 0.00314209 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891369 | AAGGCTCAGTCCAGA[C/T]GGGCAGTGGGAGGAG | 402682 |
| rs747125523 | snp | G/T | 3.7154e-05 | 0.00430994 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891303 | GTGTACGGGGGCCAT[G/T]GTGGGGCCTTGGGGT | 402682 |
| rs747346978 | snp | A/G/T | 3.31891e-05 | 0.00407353 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888399 | GTGAGGAGGGCAGAC[A/G/T]CCCAAGCTTTGTTGC | 402682 |
| rs747406605 | in-del | -/AATAAA | 4.01574e-05 | 0.00448075 | intron-variant, cds-indel | UFSP1, SRRT | GRCh38.p7 | 7:100888644 | ATCAGCCTTACTGCT[-/AATAAA]AGCACTTCCACAGGG | 402682 |
| rs747439448 | snp | C/T | 1.65157e-05 | 0.0028736 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888336 | TGGTCGAGGGAACTA[C/T]GATGCCTTCCGAGGC | 402682 |
| rs747483131 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890447 | AGGGAGGACGCACGG[A/G]GAAATGCAGGCGACC | 402682 |
| rs747583946 | snp | C/G/T | 6.68889e-05 | 0.00578279 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889077 | CCTGGCATCTGCGTC[C/G/T]CCCCCAACCATGACT | 402682 |
| rs747600428 | snp | C/T | 3.18426e-05 | 0.00399002 | missense | UFSP1 | GRCh38.p7 | 7:100889271 | GGGGCTTGTCGCCCA[C/T]GTCCTCCAGGGCCGC | 402682 |
| rs747858493 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889003 | CAGTAGTGAGGGTCC[A/G]ATACCAGGACATAGG | 402682 |
| rs748149805 | snp | A/G | 3.39864e-05 | 0.00412214 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890207 | GGACATGGGGGTCCC[A/G]CCGGGGTCACAGGTC | 402682 |
| rs748192565 | snp | C/G | 1.71959e-05 | 0.00293217 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889138 | AGCCTCTCCAGCTCC[C/G]CGTGCAGCCCCACTC | 402682 |
| rs748359177 | snp | A/G | 3.98176e-05 | 0.00446175 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891382 | GACGGGCAGTGGGAG[A/G]AGGTGGCCCCCAACT | 402682 |
| rs748465952 | snp | A/G | 1.81566e-05 | 0.00301296 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891038 | GGAGGCCGGGCCTCG[A/G]AGCAGCCTCCCCATG | 402682 |
| rs748536494 | in-del | -/CGC | 2.45041e-05 | 0.00350021 | cds-indel, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890314 | TCGGCCTTCCACTGG[-/CGC]TCCGCCTCGTCGAGC | 402682 |
| rs748675827 | snp | A/G | 3.06678e-05 | 0.00391573 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890375 | CGGGAGGGGAGGACG[A/G]CACGAGGAAGGTCGG | 402682 |
| rs748728288 | snp | C/G | 4.25469e-05 | 0.00461212 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888667 | CACTTCCACAGGGCT[C/G]CTGACTCTCGTGTGT | 402682 |
| rs748830679 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890607 | CAGAGGGGACAGGAG[A/G]GGGAGGTTGGGGGAA | 402682 |
| rs748979312 | snp | C/T | 1.65094e-05 | 0.00287305 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888315 | CCCCCATGCCCCGTA[C/T]GGTGCTGGTCGAGGG | 402682 |
| rs749004073 | snp | C/G | 1.9554e-05 | 0.00312676 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891356 | GCGGAAGGAAGGGAA[C/G]GCTCAGTCCAGACGG | 402682 |
| rs749279313 | snp | C/T | 7.05953e-05 | 0.00594076 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888796 | CCAGTGGGAGGTACA[C/T]AGGTGCGTGTCTGGG | 402682 |
| rs749502381 | snp | G/T | 7.35443e-05 | 0.00606356 | missense | UFSP1 | GRCh38.p7 | 7:100889195 | TGGGGCCCTCCGAAG[G/T]GAGCGAGGCAGAGGC | 402682 |
| rs749561922 | in-del | -/G | 3.30666e-05 | 0.00406598 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888573 | CCGTTCCTCAGTCCT[-/G]TATCATCCATACTTG | 402682 |
| rs749597355 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888928 | TCAAAGGCTGCACTC[A/G]CCTCTTGCCAGCCCA | 402682 |
| rs749635970 | snp | C/G | 3.44465e-05 | 0.00414995 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891181 | TACCGGTGGCGCTGA[C/G]CAATTTGGGGAGGAA | 402682 |
| rs749801557 | in-del | -/AGCCCCGGA | | | cds-indel | UFSP1 | GRCh38.p7 | 7:100889241 | CGATCCAGTCCCGGG[-/AGCCCCGGA]AGCCGGGGGGCTTGT | 402682 |
| rs749844262 | snp | A/C | 1.73501e-05 | 0.00294529 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891067 | TGGGTGAAGCCTGGG[A/C]AGGTGCTGGGAGCCT | 402682 |
| rs749882379 | in-del | -/C | 3.38776e-05 | 0.00411554 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889116 | ACCCCCTGCGAAGTG[-/C]GAGTAAAGCCTCTCC | 402682 |
| rs749884996 | snp | A/G | 6.49751e-05 | 0.00569942 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891153 | TCCCAGCCGCTGCCC[A/G]CTGGCCCCTGCATAC | 402682 |
| rs750298230 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888981 | ACTGGGGCTTTTTGG[A/G]GTGCCCCAGTAGTGA | 402682 |
| rs750386139 | snp | A/G | 1.83149e-05 | 0.00302607 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891257 | CTCCAGCGGCCGCAG[A/G]TCCAGACTAACGTAC | 402682 |
| rs750493660 | snp | C/T | 2.53514e-05 | 0.00356021 | synonymous-codon, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890319 | CTTCCACTGGCGCTC[C/T]GCCTCGTCGAGCGTG | 402682 |
| rs750571389 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890652 | AATGGTTGACCGTTA[C/T]AGCCCCAATGGGGGG | 402682 |
| rs751072333 | snp | A/C | 3.88999e-05 | 0.00441004 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891349 | GATCCCTGCGGAAGG[A/C]AGGGAAGGCTCAGTC | 402682 |
| rs751074502 | snp | C/T | 1.64792e-05 | 0.00287042 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888994 | GGAGTGCCCCAGTAG[C/T]GAGGGTCCAATACCA | 402682 |
| rs751236171 | snp | C/T | 1.83273e-05 | 0.00302709 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891280 | TAACGTACTGCTGAG[C/T]CCCCGCCGTGTACGG | 402682 |
| rs751247569 | snp | C/G | 1.70627e-05 | 0.00292079 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890181 | ACAGCTAGGGGGCCG[C/G]GCGGAGCGGAGGACA | 402682 |
| rs751446699 | in-del | -/C | 1.674e-05 | 0.00289305 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889076 | ACCTGGCATCTGCGT[-/C]CCCCCCAACCATGAC | 402682 |
| rs751544119 | snp | A/G | 1.75084e-05 | 0.0029587 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888831 | GAGAATCTCAGTTCT[A/G]TAACTTCGTCCTCAG | 402682 |
| rs751881061 | snp | C/T | 7.12606e-05 | 0.00596869 | missense | UFSP1 | GRCh38.p7 | 7:100889178 | CGTGGCAGAGGCGTC[C/T]CTGGGGCCCTCCGAA | 402682 |
| rs752042824 | snp | C/G/T | 8.51642e-05 | 0.00652501 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889130 | GCGAGTAAAGCCTCT[C/G/T]CAGCTCCCCGTGCAG | 402682 |
| rs752198723 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890781 | AACAACAAAGGCGTG[C/G]GGGTCCCTGAGAAGG | 402682 |
| rs752346276 | snp | A/C | 1.95204e-05 | 0.00312407 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891354 | CTGCGGAAGGAAGGG[A/C]AGGCTCAGTCCAGAC | 402682 |
| rs752606964 | snp | A/G | 2.75478e-05 | 0.00371122 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890347 | GTGTCTGCGGCCAGG[A/G]CGCCCAGCGAGGCGG | 402682 |
| rs752665876 | in-del | -/C | 1.64768e-05 | 0.00287021 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888985 | GGGCTTTTTGGAGTG[-/C]CCCAGTAGTGAGGGT | 402682 |
| rs752697669 | snp | C/T | 1.65704e-05 | 0.00287836 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888381 | TGGGAAACCTCGCAA[C/T]AGGTGAGGAGGGCAG | 402682 |
| rs753009609 | snp | C/G/T | 8.24523e-05 | 0.00642029 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888559 | TTTTGAGCCGTCCCC[C/G/T]GTTCCTCAGTCCTGT | 402682 |
| rs753171113 | snp | G/T | 3.30142e-05 | 0.00406276 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888463 | CTCATCCTGTACCTC[G/T]CACCTCACAGGATGG | 402682 |
| rs753200799 | snp | C/T | 0.000180005 | 0.00948526 | missense | UFSP1 | GRCh38.p7 | 7:100889186 | AGGCGTCCCTGGGGC[C/T]CTCCGAAGTGAGCGA | 402682 |
| rs753217441 | snp | A/G | 2.45059e-05 | 0.00350034 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889248 | GTCCCGGGAGCCCCG[A/G]AAGCCGGGGGGCTTG | 402682 |
| rs753346235 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888437 | AGACTCCCTTTTGGG[A/G]GCCCTCAGCTCTCAT | 402682 |
| rs753495271 | snp | A/G | 1.69934e-05 | 0.00291486 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889124 | CGAAGTGCGAGTAAA[A/G]CCTCTCCAGCTCCCC | 402682 |
| rs753577019 | snp | A/G | 1.6501e-05 | 0.00287232 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888906 | CAGGTTGTAGAAGGA[A/G]TTGGGGTCAAAGGCT | 402682 |
| rs753684755 | snp | C/G | 8.39948e-05 | 0.00648 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891141 | CCACTCCCCTCCTCC[C/G]AGCCGCTGCCCGCTG | 402682 |
| rs753868674 | snp | G/T | 0.000250847 | 0.0111964 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891026 | GGAGGGGCAGGGGGA[G/T]GCCGGGCCTCGGAGC | 402682 |
| rs753924962 | snp | A/G | 2.50266e-05 | 0.00353733 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889251 | CCGGGAGCCCCGGAA[A/G]CCGGGGGGCTTGTCG | 402682 |
| rs754104875 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890777 | TTCAAACAACAAAGG[C/T]GTGGGGGTCCCTGAG | 402682 |
| rs754163923 | snp | C/T | 1.83565e-05 | 0.00302951 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891283 | CGTACTGCTGAGCCC[C/T]CGCCGTGTACGGGGG | 402682 |
| rs754408033 | snp | A/G | 7.81891e-05 | 0.00625208 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889315 | AGTCCAGGTACGCCC[A/G]CGGGCTGGCCCTCTG | 402682 |
| rs754520614 | snp | C/T | 4.97508e-05 | 0.00498728 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889050 | TACGCAGACTCCCAG[C/T]AAGGCCTTGGACCTG | 402682 |
| rs754539119 | snp | C/G/T | 3.29578e-05 | 0.00405931 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889000 | CCCCAGTAGTGAGGG[C/G/T]CCAATACCAGGACAT | 402682 |
| rs754626953 | snp | A/C/T | 3.66456e-05 | 0.00428039 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891281 | AACGTACTGCTGAGC[A/C/T]CCCGCCGTGTACGGG | 402682 |
| rs754629123 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888922 | TTGGGGTCAAAGGCT[A/G]CACTCACCTCTTGCC | 402682 |
| rs754726644 | snp | A/G | 2.69371e-05 | 0.00366985 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890340 | GTCGAGCGTGTCTGC[A/G]GCCAGGGCGCCCAGC | 402682 |
| rs754799074 | snp | C/T | 1.98002e-05 | 0.00314638 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888639 | GTACGATCAGCCTTA[C/T]TGCTAATAAAAGCAC | 402682 |
| rs754815639 | snp | A/G | 3.40194e-05 | 0.00412414 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890189 | GGGGCCGGGCGGAGC[A/G]GAGGACATGGGGGTC | 402682 |
| rs754994120 | snp | C/T | 1.65356e-05 | 0.00287533 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888284 | GCCCTGCAGTCCCCA[C/T]AGGAGGCCCTCCATA | 402682 |
| rs755204109 | snp | C/T | 4.1978e-05 | 0.00458118 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888695 | TGTTACATAACTCCT[C/T]CATCCTTCCAGAGTA | 402682 |
| rs755323780 | snp | C/T | 1.65231e-05 | 0.00287424 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888450 | GGAGCCCTCAGCTCT[C/T]ATCCTGTACCTCTCA | 402682 |
| rs755342405 | snp | A/G | 3.58384e-05 | 0.00423296 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889182 | GCAGAGGCGTCCCTG[A/G]GGCCCTCCGAAGTGA | 402682 |
| rs755623259 | snp | A/G | 8.29208e-05 | 0.00643844 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888392 | GCAACAGGTGAGGAG[A/G]GCAGACGCCCAAGCT | 402682 |
| rs755694905 | in-del | -/G | 5.17023e-05 | 0.00508414 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889145 | CCAGCTCCCCGTGCA[-/G]CCCCACTCCCCGGGG | 402682 |
| rs755711164 | snp | C/T | 1.65097e-05 | 0.00287308 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888311 | CATACCCCCATGCCC[C/T]GTATGGTGCTGGTCG | 402682 |
| rs755837010 | snp | C/T | 1.66092e-05 | 0.00288172 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889057 | ACTCCCAGCAAGGCC[C/T]TGGACCTGGCATCTG | 402682 |
| rs755887940 | snp | C/G | 1.73842e-05 | 0.00294819 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888841 | GTTCTGTAACTTCGT[C/G]CTCAGTCCAAGGTGC | 402682 |
| rs755904323 | snp | C/T | 1.81391e-05 | 0.00301152 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891018 | GAGGAGGAGGAGGGG[C/T]AGGGGGAGGCCGGGC | 402682 |
| rs755906479 | snp | G/T | 6.20546e-05 | 0.00556987 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888701 | ATAACTCCTCCATCC[G/T]TCCAGAGTAACTCCT | 402682 |
| rs755996501 | snp | A/G | 2.86816e-05 | 0.00378682 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890359 | AGGGCGCCCAGCGAG[A/G]CGGGAGGGGAGGACG | 402682 |
| rs756005843 | snp | C/T | | | downstream-variant-500B, utr-variant-5-prime, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889549 | ACAGCGTCCTCCTAG[C/T]GGCGCGGAGCGACCT | 402682 |
| rs756212152 | snp | A/G | 1.8282e-05 | 0.00302336 | missense | UFSP1 | GRCh38.p7 | 7:100889193 | CCTGGGGCCCTCCGA[A/G]GTGAGCGAGGCAGAG | 402682 |
| rs756456933 | snp | C/T | 3.29804e-05 | 0.00406068 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889028 | CATAGGCTTCCGTGC[C/T]TGACCCTACGCAGAC | 402682 |
| rs756518029 | snp | C/G | 4.25505e-05 | 0.00461231 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891171 | GGCCCCTGCATACCG[C/G]TGGCGCTGAGCAATT | 402682 |
| rs756627565 | snp | A/C/G | 4.90091e-05 | 0.00495001 | missense | UFSP1 | GRCh38.p7 | 7:100889249 | TCCCGGGAGCCCCGG[A/C/G]AGCCGGGGGGCTTGT | 402682 |
| rs756662583 | snp | C/T | 1.65078e-05 | 0.00287291 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888464 | TCATCCTGTACCTCT[C/T]ACCTCACAGGATGGT | 402682 |
| rs756714777 | snp | A/G | 0.000261267 | 0.0114265 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891027 | GAGGGGCAGGGGGAG[A/G]CCGGGCCTCGGAGCA | 402682 |
| rs756918790 | in-del | -/A/CACTTTTATTATTGATGTCAAAAGCGCCAGGCTTTGCAGGG | 3.34875e-05 | 0.0040918 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889082 | ATCTGCGTCCCCCCC[lengthTooLong]AACCATGACTGGGCC | 402682 |
| rs756971338 | snp | A/G | 1.65858e-05 | 0.00287969 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888396 | CAGGTGAGGAGGGCA[A/G]ACGCCCAAGCTTTGT | 402682 |
| rs757008633 | in-del | -/T | 1.67186e-05 | 0.0028912 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888236 | ATAGTTTTGCAACTC[-/T]AACACTGATCTCTGT | 402682 |
| rs757053605 | snp | C/T | 1.65004e-05 | 0.00287227 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888907 | AGGTTGTAGAAGGAG[C/T]TGGGGTCAAAGGCTG | 402682 |
| rs757230495 | snp | A/G | 8.65254e-05 | 0.00657687 | stop-lost, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888845 | TGTAACTTCGTCCTC[A/G]GTCCAAGGTGCGCTG | 402682 |
| rs757343878 | snp | A/G | 3.31126e-05 | 0.00406881 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888575 | GTTCCTCAGTCCTGT[A/G]TCATCCATACTTGTA | 402682 |
| rs757396137 | snp | G/T | 1.65116e-05 | 0.00287324 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888307 | CCTCCATACCCCCAT[G/T]CCCCGTATGGTGCTG | 402682 |
| rs757414600 | snp | A/G | 5.21866e-05 | 0.00510789 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889254 | GGAGCCCCGGAAGCC[A/G]GGGGGCTTGTCGCCC | 402682 |
| rs757502202 | snp | A/G | 3.7143e-05 | 0.0043093 | missense | UFSP1 | GRCh38.p7 | 7:100889196 | GGGGCCCTCCGAAGT[A/G]AGCGAGGCAGAGGCT | 402682 |
| rs757512342 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890158 | CAGCCCTGAAATAAA[C/T]AGTATATACAGCTAG | 402682 |
| rs757556572 | snp | A/G | 3.29598e-05 | 0.00405941 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889004 | AGTAGTGAGGGTCCA[A/G]TACCAGGACATAGGC | 402682 |
| rs757575019 | snp | C/T | 1.8371e-05 | 0.00303071 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891284 | GTACTGCTGAGCCCC[C/T]GCCGTGTACGGGGGC | 402682 |
| rs757774787 | snp | C/T | | | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888849 | ACTTCGTCCTCAGTC[C/T]AAGGTGCGCTGCTGC | 402682 |
| rs758087529 | snp | A/C | 5.49204e-05 | 0.00523996 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891033 | CAGGGGGAGGCCGGG[A/C]CTCGGAGCAGCCTCC | 402682 |
| rs758184455 | snp | G/T | 2.70391e-05 | 0.00367679 | missense | UFSP1 | GRCh38.p7 | 7:100889258 | CCCCGGAAGCCGGGG[G/T]GCTTGTCGCCCATGT | 402682 |
| rs758411938 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888991 | TTTGGAGTGCCCCAG[C/T]AGTGAGGGTCCAATA | 402682 |
| rs758505270 | snp | A/G | 1.71217e-05 | 0.00292584 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890175 | GTATATACAGCTAGG[A/G]GGCCGGGCGGAGCGG | 402682 |
| rs758541587 | snp | C/T | 2.12222e-05 | 0.0032574 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888685 | GACTCTCGTGTGTTA[C/T]ATAACTCCTCCATCC | 402682 |
| rs758559902 | snp | C/T | 1.96992e-05 | 0.00313834 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888637 | TTGTACGATCAGCCT[C/T]ACTGCTAATAAAAGC | 402682 |
| rs758672689 | snp | A/G | 3.30278e-05 | 0.0040636 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888326 | CGTATGGTGCTGGTC[A/G]AGGGAACTATGATGC | 402682 |
| rs758776377 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890391 | CACGAGGAAGGTCGG[A/G]GATCGGACATTTGGG | 402682 |
| rs758790497 | snp | C/T | 3.4002e-05 | 0.00412309 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889126 | AAGTGCGAGTAAAGC[C/T]TCTCCAGCTCCCCGT | 402682 |
| rs758972517 | snp | A/C/G | 5.84429e-05 | 0.00540542 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891351 | TCCCTGCGGAAGGAA[A/C/G]GGAAGGCTCAGTCCA | 402682 |
| rs759173001 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890824 | GCCCCCTCCTCCTGC[C/T]CTGTCCAGTGTGAGT | 402682 |
| rs759174716 | snp | C/T | 0.000234504 | 0.0108258 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888672 | CCACAGGGCTCCTGA[C/T]TCTCGTGTGTTACAT | 402682 |
| rs759208700 | snp | C/T | 0.00014706 | 0.00857371 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888656 | GCTAATAAAAGCACT[C/T]CCACAGGGCTCCTGA | 402682 |
| rs759350046 | snp | C/T | 1.65586e-05 | 0.00287733 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888418 | AAGCTTTGTTGCCGC[C/T]TGCAGACTCCCTTTT | 402682 |
| rs759473924 | snp | A/G | 3.30764e-05 | 0.00406659 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888894 | GCTGGTCAAGCACAG[A/G]TTGTAGAAGGAGTTG | 402682 |
| rs759585250 | snp | C/G | 1.68869e-05 | 0.00290571 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889105 | ACTGGGCCCCCACCC[C/G]CTGCGAAGTGCGAGT | 402682 |
| rs759691957 | snp | C/T | 1.74766e-05 | 0.00295601 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888835 | ATCTCAGTTCTGTAA[C/T]TTCGTCCTCAGTCCA | 402682 |
| rs759848994 | snp | A/G | 1.7947e-05 | 0.00299553 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891010 | AGCTGGTGGAGGAGG[A/G]GGAGGGGCAGGGGGA | 402682 |
| rs759879231 | snp | A/G | 9.33598e-05 | 0.00683163 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889242 | GATCCAGTCCCGGGA[A/G]CCCCGGAAGCCGGGG | 402682 |
| rs760445448 | snp | A/G | 1.71009e-05 | 0.00292406 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891117 | AGAGGGGTTACACCT[A/G]GCGGGCTCCCACTCC | 402682 |
| rs760572810 | snp | G/T | 1.64751e-05 | 0.00287007 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888519 | GGAATATCGGGACCT[G/T]GATGCCCCAGACGAT | 402682 |
| rs760690014 | in-del | -/G | 1.83004e-05 | 0.00302488 | intron-variant, upstream-variant-2KB, frameshift-variant, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891030 | GGGCAGGGGGAGGCC[-/G]GGCCTCGGAGCAGCC | 402682 |
| rs760762283 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888952 | CAGCCCACCCACCCA[A/G]CAGCCTGTAGTTCAC | 402682 |
| rs760776254 | in-del | -/G | 1.65081e-05 | 0.00287293 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888902 | GCACAGGTTGTAGAA[-/G]GGAGTTGGGGTCAAA | 402682 |
| rs760832708 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890660 | ACCGTTATAGCCCCA[A/G]TGGGGGGTGCTACCC | 402682 |
| rs760887426 | snp | A/G | 4.24511e-05 | 0.00460693 | missense, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890281 | CAGTGCACCATGTAG[A/G]AGCTCCAGCGGTGGA | 402682 |
| rs760925306 | snp | A/G | 1.65132e-05 | 0.00287339 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888900 | CAAGCACAGGTTGTA[A/G]AAGGAGTTGGGGTCA | 402682 |
| rs760925378 | snp | C/T | 0.000138101 | 0.00830852 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891230 | GGCCTGGGCGCGCAG[C/T]CCCCGCCGCACCTCC | 402682 |
| rs761249487 | snp | C/T | 1.65441e-05 | 0.00287607 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888439 | ACTCCCTTTTGGGAG[C/T]CCTCAGCTCTCATCC | 402682 |
| rs761330801 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888550 | GTTGATTTCTTTTGA[A/G]CCGTCCCCCGTTCCT | 402682 |
| rs761344630 | snp | C/G | 2.13136e-05 | 0.0032644 | missense | UFSP1 | GRCh38.p7 | 7:100889222 | AGGCTGGCCTCCACG[C/G]AGCCGATCCAGTCCC | 402682 |
| rs761506074 | snp | A/G | | | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889173 | GGGTACGTGGCAGAG[A/G]CGTCCCTGGGGCCCT | 402682 |
| rs761521455 | snp | A/G | 1.85118e-05 | 0.0030423 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891250 | GCCGCACCTCCAGCG[A/G]CCGCAGGTCCAGACT | 402682 |
| rs761585712 | snp | A/C | 4.94222e-05 | 0.00497078 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888966 | AGCAGCCTGTAGTTC[A/C]CTGGGGCTTTTTGGA | 402682 |
| rs761659852 | snp | A/G | 1.8946e-05 | 0.00307777 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891324 | GCCTTGGGGTCTCGG[A/G]GCTCATTGGGATCCC | 402682 |
| rs761910805 | snp | G/T | 0.000100022 | 0.00707113 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888247 | AACTCAACACTGATC[G/T]CTGTCATAGCTGGTG | 402682 |
| rs761967599 | snp | A/G | 9.07482e-05 | 0.00673542 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889322 | GTACGCCCGCGGGCT[A/G]GCCCTCTGGCCACGA | 402682 |
| rs761994475 | in-del | -/G | 2.11387e-05 | 0.00325099 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888661 | AAAAGCACTTCCACA[-/G]GGGCTCCTGACTCTC | 402682 |
| rs762241314 | snp | C/G | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891518 | TCAAGCGCTCCGTCT[C/G]CTTCCGTTTCCCTCA | 402682 |
| rs762304635 | snp | A/G | 0.000182849 | 0.00955986 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890947 | TGTGGCCGTAGGGGA[A/G]GAGGCCGTGTTCACA | 402682 |
| rs762437365 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890474 | GACCACGTGGGACGG[C/T]GGCAAGAGGATCAGG | 402682 |
| rs762453282 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890212 | TGGGGGTCCCGCCGG[C/G]GTCACAGGTCTGAGC | 402682 |
| rs762461965 | snp | C/G | 2.3523e-05 | 0.00342943 | synonymous-codon, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890301 | CCAGCGGTGGAACTC[C/G]GCCTTCCACTGGCGC | 402682 |
| rs762471418 | snp | C/T | 1.79835e-05 | 0.00299857 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888612 | TGTCCTATGAAGCTC[C/T]GAGAATTTTTTGTAC | 402682 |
| rs762549853 | snp | C/T | 1.83138e-05 | 0.00302599 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891258 | TCCAGCGGCCGCAGG[C/T]CCAGACTAACGTACT | 402682 |
| rs762631828 | snp | C/G | 5.14178e-05 | 0.00507014 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889297 | GCCGCCTGTACGGCG[C/G]CCAGTCCAGGTACGC | 402682 |
| rs762633866 | snp | C/G/T | 3.29746e-05 | 0.00406035 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888556 | TTCTTTTGAGCCGTC[C/G/T]CCCGTTCCTCAGTCC | 402682 |
| rs762688142 | snp | C/T | 1.65477e-05 | 0.00287638 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889037 | CCGTGCCTGACCCTA[C/T]GCAGACTCCCAGCAA | 402682 |
| rs762750896 | snp | C/T | 8.4023e-05 | 0.00648108 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889091 | CCCCCCCAACCATGA[C/T]TGGGCCCCCACCCCC | 402682 |
| rs762864348 | in-del | -/T | 1.67003e-05 | 0.00288962 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889075 | GACCTGGCATCTGCG[-/T]CCCCCCCAACCATGA | 402682 |
| rs762923157 | in-del | -/G | 1.93127e-05 | 0.0031074 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891343 | CATTGGGATCCCTGC[-/G]GAAGGAAGGGAAGGC | 402682 |
| rs762929614 | snp | A/G | 7.02333e-05 | 0.00592552 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890969 | GTGTTCACAGCCGCC[A/G]GAGGTGGGAGAGGAA | 402682 |
| rs763034170 | snp | C/G | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891342 | TCATTGGGATCCCTG[C/G]GGAAGGAAGGGAAGG | 402682 |
| rs763098505 | snp | C/G | 2.59562e-05 | 0.00360242 | missense, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890327 | GGCGCTCCGCCTCGT[C/G]GAGCGTGTCTGCGGC | 402682 |
| rs763434462 | snp | A/G | 1.68046e-05 | 0.00289862 | stop-gained, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888869 | TGCGCTGCTGCTGTT[A/G]GGAGCTAAGGCTGGT | 402682 |
| rs763478287 | snp | C/G | 1.6552e-05 | 0.00287676 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888427 | TGCCGCCTGCAGACT[C/G]CCTTTTGGGAGCCCT | 402682 |
| rs763581880 | snp | A/T | 1.74698e-05 | 0.00295544 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889162 | CCCACTCCCCGGGGT[A/T]CGTGGCAGAGGCGTC | 402682 |
| rs763595505 | snp | A/G | 1.76064e-05 | 0.00296697 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888816 | GCGTGTCTGGGACCC[A/G]AGAATCTCAGTTCTG | 402682 |
| rs763750795 | snp | A/G | 3.31796e-05 | 0.00407292 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888393 | CAACAGGTGAGGAGG[A/G]CAGACGCCCAAGCTT | 402682 |
| rs763850441 | snp | C/G | 4.95127e-05 | 0.00497533 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888904 | CACAGGTTGTAGAAG[C/G]AGTTGGGGTCAAAGG | 402682 |
| rs763916652 | in-del | -/C | 1.674e-05 | 0.00289305 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889075 | ACCTGGCATCTGCGT[-/C]CCCCCCCAACCATGA | 402682 |
| rs763940469 | snp | C/G | 0.000126334 | 0.00794678 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891121 | GGGTTACACCTGGCG[C/G]GCTCCCACTCCCCTC | 402682 |
| rs763956991 | snp | G/T | 0.000251477 | 0.0112105 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891021 | GAGGAGGAGGGGCAG[G/T]GGGAGGCCGGGCCTC | 402682 |
| rs764156092 | snp | C/T | | | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891145 | TCCCCTCCTCCCAGC[C/T]GCTGCCCGCTGGCCC | 402682 |
| rs764237539 | snp | A/C | 1.64746e-05 | 0.00287002 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888954 | GCCCACCCACCCAGC[A/C]GCCTGTAGTTCACTG | 402682 |
| rs764437248 | snp | C/G | 1.84154e-05 | 0.00303436 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889314 | CAGTCCAGGTACGCC[C/G]GCGGGCTGGCCCTCT | 402682 |
| rs764483745 | snp | C/T | 2.12936e-05 | 0.00326287 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888673 | CACAGGGCTCCTGAC[C/T]CTCGTGTGTTACATA | 402682 |
| rs764565663 | snp | C/T | 1.74509e-05 | 0.00295384 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888838 | TCAGTTCTGTAACTT[C/T]GTCCTCAGTCCAAGG | 402682 |
| rs764884702 | snp | A/G | 1.65296e-05 | 0.00287481 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888445 | TTTTGGGAGCCCTCA[A/G]CTCTCATCCTGTACC | 402682 |
| rs764893294 | snp | C/T | 1.78125e-05 | 0.00298428 | missense | UFSP1 | GRCh38.p7 | 7:100889177 | ACGTGGCAGAGGCGT[C/T]CCTGGGGCCCTCCGA | 402682 |
| rs764921031 | snp | C/G | 1.6492e-05 | 0.00287154 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889033 | GCTTCCGTGCCTGAC[C/G]CTACGCAGACTCCCA | 402682 |
| rs765017679 | in-del | -/A | 4.94466e-05 | 0.00497201 | frameshift-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888923 | GGGGTCAAAGGCTGC[-/A]ACTCACCTCTTGCCA | 402682 |
| rs765149091 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888971 | CCTGTAGTTCACTGG[G/T]GCTTTTTGGAGTGCC | 402682 |
| rs765169181 | snp | A/G | 1.84266e-05 | 0.00303528 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891253 | GCACCTCCAGCGGCC[A/G]CAGGTCCAGACTAAC | 402682 |
| rs765393282 | snp | A/G/T | 3.32924e-05 | 0.00407987 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888253 | ACACTGATCTCTGTC[A/G/T]TAGCTGGTGCTGTCC | 402682 |
| rs765451336 | snp | A/G | 1.71935e-05 | 0.00293197 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | ACHE, UFSP1 | GRCh38.p7 | 7:100890164 | TGAAATAAATAGTAT[A/G]TACAGCTAGGGGGCC | 402682 |
| rs765776358 | snp | A/G/T | 4.28204e-05 | 0.00462695 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888677 | GGGCTCCTGACTCTC[A/G/T]TGTGTTACATAACTC | 402682 |
| rs765871813 | snp | C/T | 1.95532e-05 | 0.0031267 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888635 | TTTTGTACGATCAGC[C/T]TTACTGCTAATAAAA | 402682 |
| rs765871887 | snp | G/T | 5.00138e-05 | 0.00500044 | missense, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890315 | CGGCCTTCCACTGGC[G/T]CTCCGCCTCGTCGAG | 402682 |
| rs765969200 | snp | A/G | | | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888719 | CAGAGTAACTCCTGA[A/G]GTGTTGCTCAGCCCT | 402682 |
| rs766028443 | snp | C/T | 1.82998e-05 | 0.00302482 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891276 | AGACTAACGTACTGC[C/T]GAGCCCCCGCCGTGT | 402682 |
| rs766065934 | snp | C/G | 1.65674e-05 | 0.00287809 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888377 | ATCCTGGGAAACCTC[C/G]CAACAGGTGAGGAGG | 402682 |
| rs766263166 | snp | C/T | 3.31044e-05 | 0.0040683 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888279 | TGTCCGCCCTGCAGT[C/T]CCCACAGGAGGCCCT | 402682 |
| rs766444226 | snp | A/T | 1.94441e-05 | 0.00311796 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891345 | TTGGGATCCCTGCGG[A/T]AGGAAGGGAAGGCTC | 402682 |
| rs766549263 | snp | A/G | 0.000160888 | 0.00896762 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890988 | GTGGGAGAGGAAGAG[A/G]AGGAGAAGCTGGTGG | 402682 |
| rs766569218 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890746 | TTATAAAAGAATACT[A/G]GCTTTTCCATTTCCA | 402682 |
| rs766635245 | snp | A/G/T | 0.000275027 | 0.0117236 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888686 | ACTCTCGTGTGTTAC[A/G/T]TAACTCCTCCATCCT | 402682 |
| rs767110832 | snp | C/T | 1.69023e-05 | 0.00290704 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889107 | TGGGCCCCCACCCCC[C/T]GCGAAGTGCGAGTAA | 402682 |
| rs767202427 | snp | A/G | 1.65886e-05 | 0.00287993 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889051 | ACGCAGACTCCCAGC[A/G]AGGCCTTGGACCTGG | 402682 |
| rs767515571 | snp | A/G | 1.65649e-05 | 0.00287788 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888380 | CTGGGAAACCTCGCA[A/G]CAGGTGAGGAGGGCA | 402682 |
| rs767567499 | snp | G/T | 1.74531e-05 | 0.00295402 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888837 | CTCAGTTCTGTAACT[G/T]CGTCCTCAGTCCAAG | 402682 |
| rs767659912 | snp | A/G | 1.7093e-05 | 0.00292339 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891105 | TAGGGGGAGAAGAGA[A/G]GGGTTACACCTGGCG | 402682 |
| rs767691904 | snp | G/T | 1.65272e-05 | 0.0028746 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888896 | TGGTCAAGCACAGGT[G/T]GTAGAAGGAGTTGGG | 402682 |
| rs767748040 | snp | A/G | 5.3815e-05 | 0.00518697 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891012 | CTGGTGGAGGAGGAG[A/G]AGGGGCAGGGGGAGG | 402682 |
| rs767778390 | in-del | -/CT | 0.000191783 | 0.00979055 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888672 | CCACAGGGCTCCTGA[-/CT]CTCGTGTGTTACATA | 402682 |
| rs767835633 | snp | C/T | 2.37634e-05 | 0.0034469 | synonymous-codon | UFSP1 | GRCh38.p7 | 7:100889245 | CCAGTCCCGGGAGCC[C/T]CGGAAGCCGGGGGGC | 402682 |
| rs767900802 | snp | C/T | 1.80664e-05 | 0.00300547 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889299 | CGCCTGTACGGCGGC[C/T]AGTCCAGGTACGCCC | 402682 |
| rs768438948 | snp | C/T | 6.14912e-05 | 0.00554453 | missense | UFSP1 | GRCh38.p7 | 7:100889267 | CCGGGGGGCTTGTCG[C/T]CCATGTCCTCCAGGG | 402682 |
| rs768601571 | snp | A/G | 1.64754e-05 | 0.00287009 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888532 | CTGGATGCCCCAGAC[A/G]ATGTTGATTTCTTTT | 402682 |
| rs768680063 | snp | C/G | 1.98065e-05 | 0.00314688 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891373 | CTCAGTCCAGACGGG[C/G]AGTGGGAGGAGGTGG | 402682 |
| rs768697353 | snp | C/T | 1.67019e-05 | 0.00288975 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888241 | TTTTGCAACTCAACA[C/T]TGATCTCTGTCATAG | 402682 |
| rs768786089 | snp | A/C | 1.9281e-05 | 0.00310486 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891234 | TGGGCGCGCAGCCCC[A/C]GCCGCACCTCCAGCG | 402682 |
| rs769055515 | in-del | -/TAA | 2.00854e-05 | 0.00316896 | intron-variant, cds-indel | UFSP1, SRRT | GRCh38.p7 | 7:100888643 | GATCAGCCTTACTGC[-/TAA]TAAAAGCACTTCCAC | 402682 |
| rs769086789 | in-del | -/AGCCCCGGA | 0 | 0 | cds-indel | UFSP1 | GRCh38.p7 | 7:100889240 | CGATCCAGTCCCGGG[-/AGCCCCGGA]AGCCCCGGAAGCCGG | 402682 |
| rs769110040 | snp | C/T | 1.65195e-05 | 0.00287393 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888339 | TCGAGGGAACTATGA[C/T]GCCTTCCGAGGCCAG | 402682 |
| rs769119012 | snp | A/C | 8.48626e-05 | 0.00651338 | missense, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890282 | AGTGCACCATGTAGG[A/C]GCTCCAGCGGTGGAA | 402682 |
| rs769316988 | snp | G/T | 1.75965e-05 | 0.00296613 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888604 | TACTACCTTGTCCTA[G/T]GAAGCTCTGAGAATT | 402682 |
| rs769353349 | snp | C/T | 3.4013e-05 | 0.00412376 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889274 | GCTTGTCGCCCATGT[C/T]CTCCAGGGCCGCCTG | 402682 |
| rs769357889 | snp | C/T | 1.85855e-05 | 0.00304834 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891302 | CGTGTACGGGGGCCA[C/T]TGTGGGGCCTTGGGG | 402682 |
| rs769544583 | snp | C/T | 3.81119e-05 | 0.00436515 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891330 | GGGTCTCGGGGCTCA[C/T]TGGGATCCCTGCGGA | 402682 |
| rs769567811 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888663 | AAAGCACTTCCACAG[A/G]GCTCCTGACTCTCGT | 402682 |
| rs769611284 | snp | A/G | 3.98319e-05 | 0.00446255 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891383 | ACGGGCAGTGGGAGG[A/G]GGTGGCCCCCAACTC | 402682 |
| rs769776481 | snp | A/G | 1.72042e-05 | 0.00293288 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889140 | CCTCTCCAGCTCCCC[A/G]TGCAGCCCCACTCCC | 402682 |
| rs769850872 | snp | C/G | 3.31752e-05 | 0.00407265 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888410 | AGACGCCCAAGCTTT[C/G]TTGCCGCCTGCAGAC | 402682 |
| rs770254716 | snp | C/T | 1.69015e-05 | 0.00290696 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888864 | CAAGGTGCGCTGCTG[C/T]TGTTGGGAGCTAAGG | 402682 |
| rs770340900 | snp | A/C | 1.79754e-05 | 0.0029979 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891041 | GGCCGGGCCTCGGAG[A/C]AGCCTCCCCATGGGT | 402682 |
| rs770342649 | snp | A/G | 1.76372e-05 | 0.00296956 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888810 | ATAGGTGCGTGTCTG[A/G]GACCCGAGAATCTCA | 402682 |
| rs770381505 | in-del | -/CT | 1.65113e-05 | 0.00287322 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888460 | GCTCTCATCCTGTAC[-/CT]CTCACCTCACAGGAT | 402682 |
| rs770420898 | snp | A/G | 1.76555e-05 | 0.0029711 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888799 | GTGGGAGGTACATAG[A/G]TGCGTGTCTGGGACC | 402682 |
| rs770446168 | snp | A/G | 1.80374e-05 | 0.00300306 | synonymous-codon, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890247 | ATCCTGCTTGCTGTA[A/G]TGGTCGAACTGGTTC | 402682 |
| rs770483500 | snp | A/G | 0.000118617 | 0.00770029 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890907 | CCTTCCCCACGGTCC[A/G]ACCACTCATTAGAGG | 402682 |
| rs770816945 | snp | C/T | 1.73204e-05 | 0.00294277 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889149 | CTCCCCGTGCAGCCC[C/T]ACTCCCCGGGGTACG | 402682 |
| rs770891615 | snp | A/G | 1.72184e-05 | 0.00293409 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891088 | CTGGGAGCCTCCGAG[A/G]CTAGGGGGAGAAGAG | 402682 |
| rs770907112 | snp | C/T | 3.37075e-05 | 0.00410519 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889096 | CCAACCATGACTGGG[C/T]CCCCACCCCCTGCGA | 402682 |
| rs770917997 | snp | A/T | 1.64836e-05 | 0.0028708 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888475 | CTCTCACCTCACAGG[A/T]TGGTTCGTGGAGACC | 402682 |
| rs771039143 | in-del | -/C | 0.00022409 | 0.0105827 | intron-variant, upstream-variant-2KB, frameshift-variant, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891072 | AAGCCTGGGCAGGTG[-/C]CTGGGAGCCTCCGAG | 402682 |
| rs771427779 | snp | A/G | 2.85335e-05 | 0.00377703 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891193 | TGAGCAATTTGGGGA[A/G]GAAGCGGTTCCAGAA | 402682 |
| rs771628060 | snp | C/T | 1.7042e-05 | 0.00291903 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888858 | TCAGTCCAAGGTGCG[C/T]TGCTGCTGTTGGGAG | 402682 |
| rs772002628 | snp | C/G/T | 0.000196807 | 0.00991805 | missense | UFSP1 | GRCh38.p7 | 7:100889214 | CGAGGCAGAGGCTGG[C/G/T]CTCCACGCAGCCGAT | 402682 |
| rs772011769 | snp | C/T | 1.64776e-05 | 0.00287028 | stop-gained, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888937 | GCACTCACCTCTTGC[C/T]AGCCCACCCACCCAG | 402682 |
| rs772090483 | snp | C/G | 6.97216e-05 | 0.00590389 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889158 | CAGCCCCACTCCCCG[C/G]GGTACGTGGCAGAGG | 402682 |
| rs772105252 | snp | C/G | 1.8463e-05 | 0.00303828 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891295 | CCCCCGCCGTGTACG[C/G]GGGCCATTGTGGGGC | 402682 |
| rs772194902 | snp | A/G | 2.2568e-05 | 0.00335909 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891212 | GCGGTTCCAGAAGGC[A/G]CAGGCCTGGGCGCGC | 402682 |
| rs772244054 | in-del | -/GAG | 0.000153882 | 0.00877024 | intron-variant, upstream-variant-2KB, cds-indel, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890985 | GAGGTGGGAGAGGAA[-/GAG]GAGGAGAAGCTGGTG | 402682 |
| rs772374617 | snp | G/T | 1.68332e-05 | 0.00290109 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888586 | CTGTATCATCCATAC[G/T]TGTACTACCTTGTCC | 402682 |
| rs772504195 | snp | A/G | 1.67298e-05 | 0.00289217 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888230 | TGAGGACATAGTTTT[A/G]CAACTCAACACTGAT | 402682 |
| rs772577841 | snp | A/C | 1.64838e-05 | 0.00287083 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889013 | GGTCCAATACCAGGA[A/C]ATAGGCTTCCGTGCC | 402682 |
| rs772662260 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890604 | GAACAGAGGGGACAG[A/G]AGGGGGAGGTTGGGG | 402682 |
| rs772758119 | snp | A/G | 1.7725e-05 | 0.00297694 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888605 | ACTACCTTGTCCTAT[A/G]AAGCTCTGAGAATTT | 402682 |
| rs772845978 | snp | A/G | 0.000114118 | 0.00755289 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889282 | CCCATGTCCTCCAGG[A/G]CCGCCTGTACGGCGG | 402682 |
| rs773094927 | snp | C/T | 2.00142e-05 | 0.00316334 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891389 | AGTGGGAGGAGGTGG[C/T]CCCCAACTCCACGGG | 402682 |
| rs773229224 | in-del | -/C | 2.13077e-05 | 0.00326395 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888676 | AGGGCTCCTGACTCT[-/C]GTGTGTTACATAACT | 402682 |
| rs773254333 | snp | C/T | 1.92095e-05 | 0.0030991 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891338 | GGGCTCATTGGGATC[C/T]CTGCGGAAGGAAGGG | 402682 |
| rs773302361 | snp | A/G | 1.6557e-05 | 0.00287719 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888369 | GGGAGGTTATCCTGG[A/G]AAACCTCGCAACAGG | 402682 |
| rs773312510 | snp | A/C | 1.67531e-05 | 0.00289418 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889083 | ATCTGCGTCCCCCCC[A/C]ACCATGACTGGGCCC | 402682 |
| rs773428301 | in-del | -/G | 3.61945e-05 | 0.00425393 | intron-variant, upstream-variant-2KB, frameshift-variant, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891020 | GGAGGAGGAGGGGCA[-/G]GGGGAGGCCGGGCCT | 402682 |
| rs773588825 | snp | A/G | 0.000232964 | 0.0107902 | intron-variant, upstream-variant-2KB, synonymous-codon, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891060 | CTCCCCATGGGTGAA[A/G]CCTGGGCAGGTGCTG | 402682 |
| rs773761808 | snp | A/G | 1.68474e-05 | 0.00290231 | stop-gained, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888866 | AGGTGCGCTGCTGCT[A/G]TTGGGAGCTAAGGCT | 402682 |
| rs773851989 | snp | C/G | 1.76256e-05 | 0.00296859 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888814 | GTGCGTGTCTGGGAC[C/G]CGAGAATCTCAGTTC | 402682 |
| rs773870221 | snp | G/T | 0.000294305 | 0.0121271 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890955 | TAGGGGAAGAGGCCG[G/T]GTTCACAGCCGCCGG | 402682 |
| rs773976095 | snp | A/C | | | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888671 | TCCACAGGGCTCCTG[A/C]CTCTCGTGTGTTACA | 402682 |
| rs773994116 | snp | G/T | 1.81138e-05 | 0.00300941 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888615 | CCTATGAAGCTCTGA[G/T]AATTTTTTGTACGAT | 402682 |
| rs774243732 | snp | A/C/T | 3.31325e-05 | 0.00407005 | downstream-variant-500B, synonymous-codon | UFSP1, SRRT | GRCh38.p7 | 7:100888378 | TCCTGGGAAACCTCG[A/C/T]AACAGGTGAGGAGGG | 402682 |
| rs774424224 | snp | C/T | 1.68869e-05 | 0.00290571 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889104 | GACTGGGCCCCCACC[C/T]CCTGCGAAGTGCGAG | 402682 |
| rs774439726 | snp | A/G | 3.43312e-05 | 0.004143 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891091 | GGAGCCTCCGAGGCT[A/G]GGGGGAGAAGAGAGG | 402682 |
| rs774542137 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890413 | ACATTTGGGCGGGTT[A/G]AAGGGGGGGTATGAG | 402682 |
| rs774705755 | snp | C/T | 3.29592e-05 | 0.00405938 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888930 | AAAGGCTGCACTCAC[C/T]TCTTGCCAGCCCACC | 402682 |
| rs774724292 | snp | A/G | 2.71994e-05 | 0.00368768 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891197 | CAATTTGGGGAGGAA[A/G]CGGTTCCAGAAGGCG | 402682 |
| rs774926027 | snp | A/G | 1.658e-05 | 0.00287919 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888887 | AGCTAAGGCTGGTCA[A/G]GCACAGGTTGTAGAA | 402682 |
| rs775191442 | snp | C/G | 1.70026e-05 | 0.00291565 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890211 | ATGGGGGTCCCGCCG[C/G]GGTCACAGGTCTGAG | 402682 |
| rs775216067 | snp | G/T | 1.76499e-05 | 0.00297063 | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888804 | AGGTACATAGGTGCG[G/T]GTCTGGGACCCGAGA | 402682 |
| rs775290723 | snp | C/G/T | 5.23148e-05 | 0.00511421 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889159 | AGCCCCACTCCCCGG[C/G/T]GTACGTGGCAGAGGC | 402682 |
| rs775479161 | snp | C/T | 1.64768e-05 | 0.00287021 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888511 | GCCATTGTGGAATAT[C/T]GGGACCTGGATGCCC | 402682 |
| rs775592203 | snp | G/T | 4.94287e-05 | 0.00497111 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888939 | ACTCACCTCTTGCCA[G/T]CCCACCCACCCAGCA | 402682 |
| rs775643465 | snp | A/G | | | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888274 | GGTGCTGTCCGCCCT[A/G]CAGTCCCCACAGGAG | 402682 |
| rs775667028 | snp | C/G | 7.00992e-05 | 0.00591985 | utr-variant-5-prime | UFSP1 | GRCh38.p7 | 7:100889311 | GGCCAGTCCAGGTAC[C/G]CCCGCGGGCTGGCCC | 402682 |
| rs775682196 | snp | G/T | 2.1649e-05 | 0.00328999 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891216 | TTCCAGAAGGCGCAG[G/T]CCTGGGCGCGCAGCC | 402682 |
| rs775754720 | snp | C/T | 4.16328e-05 | 0.00456231 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888698 | TACATAACTCCTCCA[C/T]CCTTCCAGAGTAACT | 402682 |
| rs775852785 | snp | A/C/G | 3.34349e-05 | 0.00408859 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888233 | GGACATAGTTTTGCA[A/C/G]CTCAACACTGATCTC | 402682 |
| rs775959053 | snp | C/G | 1.69413e-05 | 0.00291039 | missense | UFSP1 | GRCh38.p7 | 7:100889221 | GAGGCTGGCCTCCAC[C/G]CAGCCGATCCAGTCC | 402682 |
| rs776005045 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889019 | ATACCAGGACATAGG[C/T]TTCCGTGCCTGACCC | 402682 |
| rs776064999 | in-del | -/C | 1.6486e-05 | 0.00287102 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888554 | TTTCTTTTGAGCCGT[-/C]CCCCCGTTCCTCAGT | 402682 |
| rs776076857 | snp | C/T | 1.90062e-05 | 0.00308265 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888627 | TGAGAATTTTTTGTA[C/T]GATCAGCCTTACTGC | 402682 |
| rs776439184 | snp | A/T | 1.64773e-05 | 0.00287026 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888541 | CCAGACGATGTTGAT[A/T]TCTTTTGAGCCGTCC | 402682 |
| rs776450194 | snp | C/T | 1.87806e-05 | 0.0030643 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891242 | CAGCCCCCGCCGCAC[C/T]TCCAGCGGCCGCAGG | 402682 |
| rs776614164 | in-del | -/C | 0.000108489 | 0.0073643 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891130 | TGGCGGGCTCCCACT[-/C]CCCCTCCTCCCAGCC | 402682 |
| rs776618868 | snp | A/T | 1.70752e-05 | 0.00292187 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888596 | CATACTTGTACTACC[A/T]TGTCCTATGAAGCTC | 402682 |
| rs776635340 | snp | C/T | 3.12671e-05 | 0.0039538 | missense | UFSP1 | GRCh38.p7 | 7:100889268 | CGGGGGGCTTGTCGC[C/T]CATGTCCTCCAGGGC | 402682 |
| rs776730102 | snp | C/T | 1.66807e-05 | 0.00288792 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888246 | CAACTCAACACTGAT[C/T]TCTGTCATAGCTGGT | 402682 |
| rs776735060 | snp | A/G | 1.89468e-05 | 0.00307783 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891323 | GGCCTTGGGGTCTCG[A/G]GGCTCATTGGGATCC | 402682 |
| rs776800902 | in-del | -/C | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888781 | GGCTTTGCAGGGACA[-/C]CAGTGGGAGGTACAT | 402682 |
| rs776832355 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889024 | AGGACATAGGCTTCC[A/G]TGCCTGACCCTACGC | 402682 |
| rs777143598 | snp | C/G | 8.26125e-05 | 0.00642646 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888340 | CGAGGGAACTATGAT[C/G]CCTTCCGAGGCCAGG | 402682 |
| rs777249086 | snp | A/G | 2.13472e-05 | 0.00326698 | synonymous-codon, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890283 | GTGCACCATGTAGGA[A/G]CTCCAGCGGTGGAAC | 402682 |
| rs777375021 | snp | C/T | | | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889139 | GCCTCTCCAGCTCCC[C/T]GTGCAGCCCCACTCC | 402682 |
| rs777627664 | snp | C/T | 2.05895e-05 | 0.00320848 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888704 | ACTCCTCCATCCTTC[C/T]AGAGTAACTCCTGAG | 402682 |
| rs777717763 | snp | A/C | 2.99585e-05 | 0.00387019 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890369 | GCGAGGCGGGAGGGG[A/C]GGACGGCACGAGGAA | 402682 |
| rs778042515 | snp | G/T | 1.72071e-05 | 0.00293313 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889141 | CTCTCCAGCTCCCCG[G/T]GCAGCCCCACTCCCC | 402682 |
| rs778251084 | snp | G/T | 3.64319e-05 | 0.00426786 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891178 | GCATACCGGTGGCGC[G/T]GAGCAATTTGGGGAG | 402682 |
| rs778273597 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888563 | GAGCCGTCCCCCGTT[C/T]CTCAGTCCTGTATCA | 402682 |
| rs778537202 | snp | A/C | 3.66267e-05 | 0.00427925 | intron-variant, upstream-variant-2KB, missense, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891028 | AGGGGCAGGGGGAGG[A/C]CGGGCCTCGGAGCAG | 402682 |
| rs778945753 | snp | A/G | 1.72946e-05 | 0.00294058 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888846 | GTAACTTCGTCCTCA[A/G]TCCAAGGTGCGCTGC | 402682 |
| rs779135120 | snp | G/T | 1.64811e-05 | 0.00287059 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888487 | AGGATGGTTCGTGGA[G/T]ACCCAAGGGCCATTG | 402682 |
| rs779182928 | snp | C/G | 1.96663e-05 | 0.00313572 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891362 | GGAAGGGAAGGCTCA[C/G]TCCAGACGGGCAGTG | 402682 |
| rs779197700 | snp | G/T | 1.65726e-05 | 0.00287855 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888576 | TTCCTCAGTCCTGTA[G/T]CATCCATACTTGTAC | 402682 |
| rs779216334 | snp | A/G | 2.62802e-05 | 0.00362483 | missense | UFSP1 | GRCh38.p7 | 7:100889255 | GAGCCCCGGAAGCCG[A/G]GGGGCTTGTCGCCCA | 402682 |
| rs779316925 | in-del | -/GGAGCTCCAGCGGT | 2.09734e-05 | 0.00323825 | frameshift-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890280 | CCAGTGCACCATGTA[-/GGAGCTCCAGCGGT]GGAACTCGGCCTTCC | 402682 |
| rs779372092 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889010 | GAGGGTCCAATACCA[A/G]GACATAGGCTTCCGT | 402682 |
| rs779457143 | snp | A/C/T | 5.51226e-05 | 0.00524964 | missense, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891286 | ACTGCTGAGCCCCCG[A/C/T]CGTGTACGGGGGCCA | 402682 |
| rs779492277 | in-del | -/CGT | 5.31096e-05 | 0.00515286 | cds-indel | UFSP1 | GRCh38.p7 | 7:100889174 | GGTACGTGGCAGAGG[-/CGT]CCCTGGGGCCCTCCG | 402682 |
| rs779561849 | snp | C/G | 1.69689e-05 | 0.00291275 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888861 | GTCCAAGGTGCGCTG[C/G]TGCTGTTGGGAGCTA | 402682 |
| rs779839348 | snp | A/C/G | 0.000262013 | 0.0114431 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100891170 | TGGCCCCTGCATACC[A/C/G]GTGGCGCTGAGCAAT | 402682 |
| rs780349145 | snp | G/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890392 | ACGAGGAAGGTCGGG[G/T]ATCGGACATTTGGGC | 402682 |
| rs780358044 | snp | G/T | 3.41746e-05 | 0.00413354 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890180 | TACAGCTAGGGGGCC[G/T]GGCGGAGCGGAGGAC | 402682 |
| rs780367208 | snp | A/C/G | 3.95501e-05 | 0.00444677 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888638 | TGTACGATCAGCCTT[A/C/G]CTGCTAATAAAAGCA | 402682 |
| rs780439991 | snp | C/T | 1.70055e-05 | 0.0029159 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889127 | AGTGCGAGTAAAGCC[C/T]CTCCAGCTCCCCGTG | 402682 |
| rs780457165 | snp | A/G | 6.78495e-05 | 0.0058241 | intron-variant, utr-variant-3-prime | UFSP1, SRRT | GRCh38.p7 | 7:100888593 | ATCCATACTTGTACT[A/G]CCTTGTCCTATGAAG | 402682 |
| rs780513216 | snp | A/G | 1.65119e-05 | 0.00287327 | downstream-variant-500B, missense | UFSP1, SRRT | GRCh38.p7 | 7:100888328 | TATGGTGCTGGTCGA[A/G]GGAACTATGATGCCT | 402682 |
| rs780529993 | snp | C/T | 1.66938e-05 | 0.00288905 | missense, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889073 | TGGACCTGGCATCTG[C/T]GTCCCCCCCAACCAT | 402682 |
| rs780605374 | in-del | -/GAG | 4.9717e-05 | 0.00498558 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888386 | AACCTCGCAACAGGT[-/GAG]GAGGGCAGACGCCCA | 402682 |
| rs780728571 | snp | A/G/T | 1.71714e-05 | 0.00293008 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890169 | TAAATAGTATATACA[A/G/T]CTAGGGGGCCGGGCG | 402682 |
| rs780824831 | in-del | -/TC | 3.33695e-05 | 0.00408456 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888245 | GCAACTCAACACTGA[-/TC]TCTGTCATAGCTGGT | 402682 |
| rs781004221 | snp | C/T | 5.47585e-05 | 0.00523223 | intron-variant, upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890343 | GAGCGTGTCTGCGGC[C/T]AGGGCGCCCAGCGAG | 402682 |
| rs781022994 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888927 | GTCAAAGGCTGCACT[C/T]ACCTCTTGCCAGCCC | 402682 |
| rs781096105 | snp | A/C | 6.79775e-05 | 0.00582959 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100890206 | AGGACATGGGGGTCC[A/C]GCCGGGGTCACAGGT | 402682 |
| rs781098533 | snp | A/G | 3.42091e-05 | 0.00413562 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891101 | AGGCTAGGGGGAGAA[A/G]AGAGGGGTTACACCT | 402682 |
| rs781300032 | snp | C/G | 0.000100388 | 0.00708407 | synonymous-codon, downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100889080 | GGCATCTGCGTCCCC[C/G]CCAACCATGACTGGG | 402682 |
| rs781473123 | snp | A/G | 1.99003e-05 | 0.00315432 | intron-variant, upstream-variant-2KB | ACHE, UFSP1 | GRCh38.p7 | 7:100891381 | AGACGGGCAGTGGGA[A/G]GAGGTGGCCCCCAAC | 402682 |
| rs781499814 | snp | C/T | 2.09321e-05 | 0.00323506 | downstream-variant-500B | UFSP1, SRRT | GRCh38.p7 | 7:100888696 | GTTACATAACTCCTC[C/T]ATCCTTCCAGAGTAA | 402682 |
| rs781604553 | snp | A/T | 1.65187e-05 | 0.00287386 | intron-variant | UFSP1, SRRT | GRCh38.p7 | 7:100888451 | GAGCCCTCAGCTCTC[A/T]TCCTGTACCTCTCAC | 402682 |
| rs796904396 | in-del | -/CCCCGCCCCTCCCCTCCCCTCCCCT | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | ACHE, UFSP1 | GRCh38.p7 | 7:100889737 | CCGCGCCCCGCCCCG[-/CCCCGCCCCTCCCCTCCCCTCCCCT]CCCCTCCCCTCCCCT | 402682 |