| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs759367529 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645280 | ATCCACTCACCATGT[A/G]CACAACCACAGTCAC | 89848 |
| rs759392634 | snp | A/C | 1.64914e-05 | 0.00287149 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640281 | CCAAGCAAACCAGAC[A/C]CTTCTGATCACCAGG | 89848 |
| rs759534950 | snp | A/G | 3.31214e-05 | 0.00406935 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649031 | TTAGCCTGTGCAGAT[A/G]AGAGAAAGGAGTCAG | 89848 |
| rs759619161 | snp | C/T | 2.57795e-05 | 0.00359014 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646169 | GAAGCCTGCTGCCGC[C/T]TCTGCTCCAGTCGTT | 89848 |
| rs759638479 | snp | A/G | 1.71897e-05 | 0.00293164 | synonymous-codon, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141639016 | AGGGACAGTGCAGCT[A/G]TCCAGGTGAGCTGGA | 89848 |
| rs759719183 | in-del | -/C | 1.65655e-05 | 0.00287793 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644665 | CGCTCAGGGACAAAG[-/C]CTACCTCGCCGTGCT | 89848 |
| rs759787161 | snp | A/T | 1.69812e-05 | 0.00291382 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644437 | GGCCTGTGCCAGGAA[A/T]GCTACAGAGGCCCAG | 89848 |
| rs759876147 | snp | A/G/T | 3.31814e-05 | 0.00407306 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649474 | GACGCCTGGAGTCGG[A/G/T]TTTGGCCCCCAGCCA | 89848 |
| rs759902074 | in-del | -/CTC | 8.38441e-05 | 0.00647418 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641678 | CCCTCTACATACAAT[-/CTC]CTCCAAGGCAAGGGC | 89848 |
| rs759965004 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640557 | TGCAGGCTTAGCCTT[C/T]GCTATAAATCCCTTG | 89848 |
| rs759992674 | snp | A/G | 1.65655e-05 | 0.00287793 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650423 | CGGAGATTGCAGGTC[A/G]GGGGTGAGGTGGGGG | 89848 |
| rs760003636 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642815 | AGGTTCAGAATCCCA[C/G]CACACACTTGGAGAT | 89848 |
| rs760082283 | snp | A/G | 4.44119e-05 | 0.00471211 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651066 | GCTGCCAGGTCTGAA[A/G]GATGCTCAGCTGTTC | 89848 |
| rs760125126 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638899 | TCCCTCTTCTCCAAC[C/T]TTCTCTTGCCCTGAC | 89848 |
| rs760139173 | snp | C/T | 4.96808e-05 | 0.00498377 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648945 | CCCCACTCATGCCCT[C/T]ATCCCTCGAACCTTG | 89848 |
| rs760165312 | snp | C/T | 1.65759e-05 | 0.00287883 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649313 | TTCTCTGTTCCCTAT[C/T]GGGATGCATACACAA | 89848 |
| rs760217270 | in-del | -/GACCTCATATGG | 0.000128123 | 0.00800282 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645167 | GAGGGGCAAAGAACA[-/GACCTCATATGG]GGCCCACTCTCAAGC | 89848 |
| rs760231612 | snp | A/G | 5.14867e-05 | 0.00507353 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643098 | CAGCATCTGGAGGTG[A/G]GGTGGGCACAGAGTT | 89848 |
| rs760257339 | snp | C/T | 1.87426e-05 | 0.0030612 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646742 | ATGGGTCAGGGGGTG[C/T]TGTGAGGAGGACCTG | 89848 |
| rs760258971 | snp | C/T | 1.65748e-05 | 0.00287874 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649396 | CCTCTGAGCCATACC[C/T]TCCTAAGCACCTGCT | 89848 |
| rs760292174 | snp | C/G | 1.67097e-05 | 0.00289043 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639982 | GTGATGGCTCCCCCA[C/G]AGACAGGAGCTGGGG | 89848 |
| rs760297967 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641615 | CCTTAAGGGTATCCC[C/T]GTCTATTCCCTCAGC | 89848 |
| rs760343161 | snp | A/G | 5.33419e-05 | 0.00516412 | stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647164 | CTGGCTGAAACTGCT[A/G]AGGTGGGGTGGGGGA | 89848 |
| rs760437166 | in-del | -/AG | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642546 | ATAGACATTTAAAAA[-/AG]AGAAAAAAAGTGGGC | 89848 |
| rs760443601 | snp | A/C | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652750 | CAGAGTTCTTCATGC[A/C]TGCTTTCTTTCTCCA | 89848 |
| rs760634197 | snp | G/T | 4.31472e-05 | 0.00464454 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645746 | CTTCTAAGTAAGGAT[G/T]GGTAGTGTTGGGGGA | 89848 |
| rs760665491 | snp | C/T | 2.24188e-05 | 0.00334797 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646594 | GACACCTGTGCCCCC[C/T]CACCTCACCCGATGC | 89848 |
| rs760710261 | snp | C/T | | | stop-gained, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645864 | CATGGCTGGCTTCAG[C/T]CAGCGCTCCACATCT | 89848 |
| rs760750187 | snp | C/T | 3.31488e-05 | 0.00407103 | splice-donor-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644572 | AATTTCCCTTTCTTA[C/T]CTGTGGGCTCTGCCC | 89848 |
| rs760758094 | in-del | -/AAC | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643507 | ATGTATATACATTAT[-/AAC]AACAGATATCTTATA | 89848 |
| rs760772622 | snp | C/G | 1.72317e-05 | 0.00293523 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649554 | CCCCAGAGAAGGTCT[C/G]TGTTGAGGAGGAGAG | 89848 |
| rs760777861 | snp | A/G | 1.7177e-05 | 0.00293056 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644455 | TACAGAGGCCCAGGA[A/G]AGACGGTGAGAGGGA | 89848 |
| rs760800991 | snp | C/G | 6.60644e-05 | 0.00574698 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640173 | ACCCCTCGTGCACTT[C/G]AAGGGAACCCCAGAG | 89848 |
| rs760856427 | snp | A/G | 1.68352e-05 | 0.00290126 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647537 | TAGAGAGAACCCCAA[A/G]ATACTGACACCACCC | 89848 |
| rs760874296 | in-del | -/AC | 1.64931e-05 | 0.00287163 | intron-variant, utr-variant-3-prime, frameshift-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141640304 | TCACCAGGTAGGAAA[-/AC]ACAGCCGGGACTGCA | 89848 |
| rs760919002 | snp | A/G | | | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638815 | GACGATGACATGAAT[A/G]AGGACACAGTAGAGA | 89848 |
| rs760999279 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640926 | ATAGAGCGTGGCAGC[C/T]GGGAGCAGGCCCCTG | 89848 |
| rs761004082 | snp | C/G | 0.000258517 | 0.0113663 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639037 | GTGAGCTGGAAACAA[C/G]GGCCAGCATGACTTA | 89848 |
| rs761011733 | snp | C/G | 2.00975e-05 | 0.00316991 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649982 | CCATCACAGAACCAA[C/G]TTCCCTTTCAAAGAC | 89848 |
| rs761037399 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649668 | TGTCTGGGAGCCCAT[C/T]AATCGATCAGCCCAT | 89848 |
| rs761055773 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649115 | TTGGCTCCACCCCTA[C/G]ACAGCCCCACCTCCC | 89848 |
| rs761111079 | snp | G/T | 0.000114883 | 0.00757815 | utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651370 | GGCGGCGGCTGCATC[G/T]CCGCTCCAGCAAGGC | 89848 |
| rs761133000 | snp | C/G | | | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640309 | AGGTAGGAAAACACA[C/G]CCGGGACTGCACTGG | 89848 |
| rs761199136 | snp | A/G | 1.65605e-05 | 0.0028775 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649039 | TGCAGATGAGAGAAA[A/G]GAGTCAGGCCCACCC | 89848 |
| rs761252999 | snp | C/T | 0.00011613 | 0.00761914 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639555 | TGCCTCCATTGCAGC[C/T]GCAGCAAGAGGCCTC | 89848 |
| rs761267623 | snp | A/G | 5.81074e-05 | 0.00538984 | stop-gained, synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646182 | GCCTCTGCTCCAGTC[A/G]TTGCAGTACCTGGTT | 89848 |
| rs761297650 | snp | A/G | 2.55588e-05 | 0.00357474 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647176 | GCTGAGGTGGGGTGG[A/G]GGAAAATACACCAGG | 89848 |
| rs761387148 | snp | A/G | 1.68323e-05 | 0.00290101 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640040 | TGGTCAGGGGTCTGG[A/G]GGAGGGCAGCCCAAG | 89848 |
| rs761387404 | snp | A/G | 4.04441e-05 | 0.00449671 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647384 | GGGAAGCTCTTAGAG[A/G]CCACAGCCCTCACCT | 89848 |
| rs761387475 | snp | A/G | 1.78188e-05 | 0.00298481 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644846 | AGGTCAGAGCCCGGG[A/G]TCCCATACCCACCTT | 89848 |
| rs761565403 | in-del | -/CA | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649724 | GCCCTCCACCCCACC[-/CA]CAGTGTCCTTGCTGG | 89848 |
| rs761623111 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638863 | ATCCAGAATGAAGGT[A/G]GGTCTAGCATAGCCC | 89848 |
| rs761663840 | snp | C/G | 5.25224e-05 | 0.0051243 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645887 | CCACATCTAAGCCAG[C/G]CCCCTGCAGCAGGGC | 89848 |
| rs761749960 | snp | A/G | 4.75953e-05 | 0.00487805 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644170 | TTATTGGGGTGGGAG[A/G]GTCAACCCAGAGGTG | 89848 |
| rs761753319 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642840 | GGAGATGACAGAGCG[G/T]GACCTGAACCAGTCA | 89848 |
| rs761858851 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640416 | CTTTCTCTCAGGTGT[C/G]TCTACCACAGGGAGC | 89848 |
| rs761884904 | snp | A/C | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645502 | CTTTTCGAGATTGCA[A/C]AGCTCATAAGTGGAG | 89848 |
| rs761890460 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650321 | GTGATATAAGAGAGG[C/T]TGGAACAAGAGGTAA | 89848 |
| rs761897649 | snp | A/G | 6.94855e-05 | 0.00589389 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647956 | GATAGGGGTGTCTGG[A/G]TTAAAACTGGCCTTG | 89848 |
| rs761951028 | snp | C/T | 1.65685e-05 | 0.00287819 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644674 | ACAAAGCCTACCTCG[C/T]CGTGCTGGTTCCGAG | 89848 |
| rs761989219 | snp | C/T | 2.13331e-05 | 0.0032659 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645768 | GTTGGGGGAGGAGCT[C/T]ACGGTTGGAGAGAGG | 89848 |
| rs762067116 | snp | C/G/T | 8.28804e-05 | 0.00643697 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649223 | GCCCACACACGTTCC[C/G/T]GCTGCCCATACAGCT | 89848 |
| rs762186023 | snp | C/T | | | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640255 | TGCCCACTCAAGAGG[C/T]AAATGGGCAGCCAAG | 89848 |
| rs762202778 | snp | C/T | | | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639076 | TGGAGAGTATCCTCT[C/T]CTCCAGCACAATCCT | 89848 |
| rs762229943 | snp | A/G | 1.80192e-05 | 0.00300154 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639653 | CTCTGTGGGCAGGTG[A/G]GGCAGGTGCTCCAGG | 89848 |
| rs762339643 | snp | C/T | 1.99376e-05 | 0.00315728 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646604 | CCCCCCCACCTCACC[C/T]GATGCCCATGGTTCT | 89848 |
| rs762363343 | snp | A/G | 1.67189e-05 | 0.00289122 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644956 | GCCTGGGCCACACAC[A/G]AAGGATTCAGGACTT | 89848 |
| rs762429286 | snp | C/T | 1.77552e-05 | 0.00297948 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646720 | CCACTCCAGGACACA[C/T]ACCTGAATGGGTCAG | 89848 |
| rs762447785 | in-del | -/CTC | 1.65883e-05 | 0.00287991 | cds-indel, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649195 | GACATCAGCCGCCTT[-/CTC]CTGTGCCAAGGCCCA | 89848 |
| rs762538530 | snp | A/G | 3.70226e-05 | 0.00430232 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641562 | GGAGGTGGTGGACGC[A/G]TCTGTAGGGAACACA | 89848 |
| rs762614109 | snp | A/G | 0.000118857 | 0.00770806 | utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651386 | CCGCTCCAGCAAGGC[A/G]GTCAGCCACTGGACT | 89848 |
| rs762718461 | snp | A/G | 1.68675e-05 | 0.00290405 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644420 | CCGGTGTAGCTGTAC[A/G]GGGCCTGTGCCAGGA | 89848 |
| rs762773489 | snp | C/T | 3.36298e-05 | 0.00410046 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644339 | CCGTCATCTACTCCA[C/T]CTTGGGCCCGGGGCA | 89848 |
| rs762774318 | snp | A/G | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644233 | CTGTTCAGGGTCAGA[A/G]AGTTCAGGTGGCCCT | 89848 |
| rs762800363 | snp | C/G | 1.65231e-05 | 0.00287424 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640161 | GACAGCAGCCTAACC[C/G]CTCGTGCACTTGAAG | 89848 |
| rs762843830 | snp | G/T | 1.88581e-05 | 0.00307062 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647414 | TGGGAGGTTGTCTGC[G/T]CCCCGCGGTGGGCAT | 89848 |
| rs762851085 | snp | A/G | 3.31466e-05 | 0.0040709 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649419 | CACCTGCTCCTTGGC[A/G]CTCCGCCCTGTACCC | 89848 |
| rs762859903 | snp | C/G/T | 5.03413e-05 | 0.00501683 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640057 | GAGGGCAGCCCAAGG[C/G/T]AGGGATGCCTGCCAT | 89848 |
| rs762942642 | snp | C/T | 8.29401e-05 | 0.00643919 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649471 | TCAGACGCCTGGAGT[C/T]GGGTTTGGCCCCCAG | 89848 |
| rs762950992 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647885 | ATCCCCTGCACCACC[C/G]ACTGTCATGGGGATC | 89848 |
| rs763005794 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638881 | TCTAGCATAGCCCCT[C/T]GCTCCCTCTTCTCCA | 89848 |
| rs763040986 | snp | C/T | | | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646508 | CCCTCCCCTCTGTAG[C/T]TCCATGACACCCTCA | 89848 |
| rs763093127 | snp | C/T | 1.68684e-05 | 0.00290412 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645919 | AGCCGGGCAGCCCCC[C/T]TCACCTGGCTCACCT | 89848 |
| rs763103727 | snp | A/G | 0.000298063 | 0.0122042 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644200 | GCCTGGGGAGTTCAG[A/G]GAGAAGGTAAGCCTC | 89848 |
| rs763180793 | snp | C/T | 2.32864e-05 | 0.00341213 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646093 | GTGCCTCACCTGTGC[C/T]CGGCGGATGCTCTCT | 89848 |
| rs763183547 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641469 | GATAGGGACAGCAGC[A/C]TCACTGGGGGTCAAG | 89848 |
| rs763225898 | snp | C/G | 1.84619e-05 | 0.00303819 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646735 | CACCTGAATGGGTCA[C/G]GGGGTGCTGTGAGGA | 89848 |
| rs763374525 | in-del | -/AGATGAGAGAA | 1.65608e-05 | 0.00287752 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649026 | CGGTTTAGCCTGTGC[-/AGATGAGAGAA]AGATGAGAGAAAGGA | 89848 |
| rs763424275 | in-del | -/CCTCACGCCCTGCCTGGG | 1.67461e-05 | 0.00289357 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644930 | TGATTGTCAGCTCAT[-/CCTCACGCCCTGCCTGGG]CCACACACGAAGGAT | 89848 |
| rs763499908 | snp | A/G | 1.65729e-05 | 0.00287857 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644682 | TACCTCGCCGTGCTG[A/G]TTCCGAGCCTGCTCA | 89848 |
| rs763540408 | snp | A/C/G | 3.31528e-05 | 0.0040713 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649314 | TCTCTGTTCCCTATT[A/C/G]GGATGCATACACAAA | 89848 |
| rs763581454 | snp | C/T | 3.29565e-05 | 0.00405921 | missense, utr-variant-3-prime, stop-gained | RELL2, FCHSD1 | GRCh38.p7 | 5:141640431 | CTCTACCACAGGGAG[C/T]AGGGAGTATGTGAGG | 89848 |
| rs763589187 | snp | C/T | 1.86788e-05 | 0.00305599 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644824 | CCCTCCTACTGCCCC[C/T]AACCCAAGGTCAGAG | 89848 |
| rs763625644 | snp | G/T | 1.88301e-05 | 0.00306834 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646745 | GGTCAGGGGGTGCTG[G/T]GAGGAGGACCTGAGG | 89848 |
| rs763634680 | snp | A/G | 1.66012e-05 | 0.00288103 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644704 | GCCTGCTCACCCAGC[A/G]ATGTGAACAGATATT | 89848 |
| rs763720485 | snp | C/G | 1.64792e-05 | 0.00287042 | stop-lost, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640443 | GAGCAGGGAGTATGT[C/G]AGGTGAGTCTGCCTG | 89848 |
| rs763767540 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141652974 | CCACCTACCAGGTTC[A/C]AGTGATTCTTCTGCT | 89848 |
| rs763873579 | snp | C/T | 3.62063e-05 | 0.00425463 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644842 | CCCAAGGTCAGAGCC[C/T]GGGGTCCCATACCCA | 89848 |
| rs764015931 | snp | A/G | 1.65759e-05 | 0.00287883 | stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649248 | ACAGCTTCCGACTTC[A/G]GCTCAGCTCCCGGAC | 89848 |
| rs764017527 | snp | A/G | 4.98235e-05 | 0.00499092 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649491 | TTGGCCCCCAGCCAC[A/G]GTGGCATCCAGCAGG | 89848 |
| rs764074403 | snp | C/T | 0.000246944 | 0.0111091 | splice-donor-variant, intron-variant | FCHSD1 | GRCh38.p7 | 5:141643000 | AGTTCCTTCCACTCA[C/T]CCCCAGGCAGGACAG | 89848 |
| rs764086935 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640187 | TGAAGGGAACCCCAG[A/G]GCTTCTGCAGAGCCA | 89848 |
| rs764131821 | snp | A/C | 1.66258e-05 | 0.00288316 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639898 | TTGTGGTCCTAAACC[A/C]CAGTGTTCCCTCCCC | 89848 |
| rs764260868 | snp | A/T | 1.73348e-05 | 0.00294399 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649563 | AGGTCTGTGTTGAGG[A/T]GGAGAGCACTCCACA | 89848 |
| rs764274007 | snp | A/G | 1.65674e-05 | 0.00287809 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650311 | GACATTACTGGTGAT[A/G]TAAGAGAGGCTGGAA | 89848 |
| rs764283802 | snp | C/T | 2.66955e-05 | 0.00365336 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647943 | CTCCCTGCTGAGGGA[C/T]AGGGGTGTCTGGGTT | 89848 |
| rs764330298 | snp | A/G | 8.24627e-05 | 0.00642063 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640312 | TAGGAAAACACAGCC[A/G]GGACTGCACTGGGCT | 89848 |
| rs764346850 | snp | C/T | 1.68459e-05 | 0.00290219 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647547 | CCCAAGATACTGACA[C/T]CACCCTTCCCCCAGA | 89848 |
| rs764448927 | snp | C/G | 0.000114883 | 0.00757815 | utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651372 | CGGCGGCTGCATCTC[C/G]GCTCCAGCAAGGCGG | 89848 |
| rs764470877 | snp | A/G | 1.78781e-05 | 0.00298977 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645097 | CAGGCTCCTCAAAGA[A/G]CTCTCCCGTCTCCTC | 89848 |
| rs764534520 | snp | A/C | 3.9165e-05 | 0.00442504 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639052 | GGGCCAGCATGACTT[A/C]GCTTGCCTTGGAGAG | 89848 |
| rs764573043 | snp | A/G | 1.65608e-05 | 0.00287752 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649040 | GCAGATGAGAGAAAG[A/G]AGTCAGGCCCACCCC | 89848 |
| rs764634134 | in-del | -/G | 1.77149e-05 | 0.0029761 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645076 | TCGTGGCCAGGGCTT[-/G]GGGGGCAGGCTCCTC | 89848 |
| rs764663159 | snp | A/G | 9.30103e-05 | 0.00681883 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646188 | GCTCCAGTCGTTGCA[A/G]TACCTGGTTGGGAAG | 89848 |
| rs764744612 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653414 | TAGTCTTTTGGTTCC[C/T]AGGTTTATTGACAAT | 89848 |
| rs764746087 | snp | A/G | 2.54832e-05 | 0.00356945 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647179 | GAGGTGGGGTGGGGG[A/G]AAATACACCAGGCTC | 89848 |
| rs764758017 | snp | A/T | 1.75718e-05 | 0.00296405 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644852 | GAGCCCGGGGTCCCA[A/T]ACCCACCTTGACCCA | 89848 |
| rs764798163 | snp | G/T | 4.4957e-05 | 0.00474093 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651084 | TGCTCAGCTGTTCCA[G/T]GAAGCGAAGCTTCAC | 89848 |
| rs764846398 | snp | A/G | 3.34879e-05 | 0.0040918 | missense, synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644936 | TCAGCTCATCCTCAC[A/G]CCCTGCCTGGGCCAC | 89848 |
| rs764848520 | snp | C/T | 7.97416e-05 | 0.00631383 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641495 | TCAAGGCTTCCCTGG[C/T]CTTCAGGTGAGGGGA | 89848 |
| rs764938323 | snp | C/T | 7.60832e-05 | 0.00616732 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641559 | GGGGGAGGTGGTGGA[C/T]GCATCTGTAGGGAAC | 89848 |
| rs764943524 | snp | A/G | 4.53587e-05 | 0.00476207 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644182 | GAGGGTCAACCCAGA[A/G]GTGCCTGGGGAGTTC | 89848 |
| rs764966273 | snp | G/T | 1.65751e-05 | 0.00287876 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649318 | TGTTCCCTATTGGGA[G/T]GCATACACAAAGTCC | 89848 |
| rs765056426 | snp | G/T | 1.94763e-05 | 0.00312054 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646756 | GCTGTGAGGAGGACC[G/T]GAGGCTGCTCCTTCT | 89848 |
| rs765214288 | snp | G/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649414 | CTAAGCACCTGCTCC[G/T]TGGCGCTCCGCCCTG | 89848 |
| rs765231861 | snp | A/G | 3.31724e-05 | 0.00407248 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650325 | TATAAGAGAGGCTGG[A/G]ACAAGAGGTAAGGTC | 89848 |
| rs765295877 | snp | A/G | | | intron-variant, synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641546 | GGCTTTAGCCGGCGG[A/G]GGAGGTGGTGGACGC | 89848 |
| rs765309159 | snp | A/G | 1.68179e-05 | 0.00289977 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640043 | TCAGGGGTCTGGGGG[A/G]GGGCAGCCCAAGGCA | 89848 |
| rs765407743 | snp | A/G/T | 5.13486e-05 | 0.00506677 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648065 | CGGGCTGCTTGCAGC[A/G/T]GCTGGGAGTACTGGG | 89848 |
| rs765431678 | snp | C/T | 0.000134662 | 0.00820444 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645903 | CCCCTGCAGCAGGGC[C/T]AGCCGGGCAGCCCCC | 89848 |
| rs765466991 | snp | A/G | 4.26858e-05 | 0.00461964 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645771 | GGGGGAGGAGCTCAC[A/G]GTTGGAGAGAGGTCC | 89848 |
| rs765639346 | snp | C/G | 4.40713e-05 | 0.00469401 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646209 | GGTTGGGAAGGCAGA[C/G]AACAGGGGTGGGTGG | 89848 |
| rs765711145 | snp | C/G | | | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639204 | CATCTCTCTCATCTA[C/G]ATATCATCAAGCCTA | 89848 |
| rs765716698 | snp | C/T | 3.65344e-05 | 0.00427386 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649585 | CACTCCACAGCTTCA[C/T]GAGACCACCCCCACC | 89848 |
| rs765723400 | snp | A/C | 1.94101e-05 | 0.00311523 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646606 | CCCCCACCTCACCCG[A/C]TGCCCATGGTTCTGG | 89848 |
| rs765738680 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650521 | GGGGAGCCAGGTTCC[C/T]AGAGTGTAACTACAC | 89848 |
| rs765813467 | snp | C/T | 1.65685e-05 | 0.00287819 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644588 | CTGTGGGCTCTGCCC[C/T]GCAGGGATTGTCACT | 89848 |
| rs765853036 | snp | C/T | 2.18243e-05 | 0.00330328 | utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651396 | AAGGCGGTCAGCCAC[C/T]GGACTCCGGAACTGG | 89848 |
| rs765859103 | in-del | -/GGC | 3.15811e-05 | 0.00397361 | cds-indel, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645852 | CTGGGCCTGGGTCAT[-/GGC]TGGCTTCAGCCAGCG | 89848 |
| rs765882575 | snp | A/C | 3.52752e-05 | 0.00419957 | intron-variant, downstream-variant-500B | FCHSD1, RELL2 | GRCh38.p7 | 5:141641574 | CGCATCTGTAGGGAA[A/C]ACACAGTTAGTGCTC | 89848 |
| rs765905768 | in-del | -/G | 3.31573e-05 | 0.00407156 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649248 | ACAGCTTCCGACTTC[-/G]GCTCAGCTCCCGGAC | 89848 |
| rs765938641 | snp | C/T | 3.32204e-05 | 0.00407542 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649123 | ACCCCTAGACAGCCC[C/T]ACCTCCCTGTTCCCC | 89848 |
| rs765967736 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650118 | AATCCTTACAACAAC[C/T]CTACATGAAGGTAAG | 89848 |
| rs765970520 | snp | C/T | 1.72255e-05 | 0.0029347 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639437 | AATGGAAATGTTACC[C/T]TCACTCCCCTCCTCC | 89848 |
| rs765970890 | snp | A/T | 1.66638e-05 | 0.00288645 | splice-donor-variant | FCHSD1 | GRCh38.p7 | 5:141641700 | AAGGCAAGGGCCCTT[A/T]CCGGCCTGAGTCGAG | 89848 |
| rs766056651 | snp | C/T | 4.98583e-05 | 0.00499266 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639574 | GCAAGAGGCCTCCAC[C/T]TGTCCGTCAGGGACG | 89848 |
| rs766104762 | snp | C/G | 5.26274e-05 | 0.00512942 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647204 | AGGCTCCTGAAGAAA[C/G]AGCTTCAGGTCTTGC | 89848 |
| rs766209386 | snp | C/T | 0.000397647 | 0.0140949 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649423 | TGCTCCTTGGCGCTC[C/T]GCCCTGTACCCCCTG | 89848 |
| rs766268818 | snp | A/G | 0.000220378 | 0.0104948 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645190 | ATGGGGCCCACTCTC[A/G]AGCACTGGTTCTATC | 89848 |
| rs766305911 | snp | C/T | 3.71692e-05 | 0.00431083 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647418 | AGGTTGTCTGCTCCC[C/T]GCGGTGGGCATGCTC | 89848 |
| rs766309175 | snp | A/G | 1.73363e-05 | 0.00294412 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648088 | GTACTGGGCTGACTG[A/G]GCGGACAGCTAGGAG | 89848 |
| rs766393615 | snp | G/T | 1.67013e-05 | 0.0028897 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644963 | CCACACACGAAGGAT[G/T]CAGGACTTGGCTGTC | 89848 |
| rs766474353 | snp | C/T | 1.69309e-05 | 0.0029095 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645920 | GCCGGGCAGCCCCCT[C/T]CACCTGGCTCACCTG | 89848 |
| rs766527426 | in-del | -/AC | 6.14156e-05 | 0.00554112 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640644 | CTTGAACAGGAAGCA[-/AC]AGTGTTATTCTTCCT | 89848 |
| rs766568574 | snp | C/G | 2.31624e-05 | 0.00340303 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646094 | TGCCTCACCTGTGCC[C/G]GGCGGATGCTCTCTC | 89848 |
| rs766598004 | snp | A/G | 3.20446e-05 | 0.00400266 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644210 | TTCAGGGAGAAGGTA[A/G]GCCTCACCTGTTCAG | 89848 |
| rs766658544 | snp | A/C/G | 6.71034e-05 | 0.00579207 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644349 | CTCCATCTTGGGCCC[A/C/G]GGGCAGCAGACGGAT | 89848 |
| rs766775767 | snp | C/T | 3.31543e-05 | 0.00407137 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644686 | TCGCCGTGCTGGTTC[C/T]GAGCCTGCTCACCCA | 89848 |
| rs766814607 | snp | A/G | 1.65619e-05 | 0.00287762 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650345 | GAGGTAAGGTCCAGA[A/G]AAAAGTCCCATACCT | 89848 |
| rs766866757 | snp | A/G | 1.89932e-05 | 0.00308159 | stop-gained, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647994 | CTGGCAGTTCCTCCT[A/G]GTAGTAATGGTCGAG | 89848 |
| rs766941038 | snp | A/G | 3.29565e-05 | 0.00405921 | missense, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640433 | CTACCACAGGGAGCA[A/G]GGAGTATGTGAGGTG | 89848 |
| rs766948144 | snp | A/C | 1.7294e-05 | 0.00294053 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642971 | TTCCTGTCTGTTAGC[A/C]TCCCAAGGCTCCCAG | 89848 |
| rs767024402 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640559 | CAGGCTTAGCCTTTG[C/T]TATAAATCCCTTGGT | 89848 |
| rs767038525 | snp | C/T | 1.65759e-05 | 0.00287883 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649241 | TGCCCATACAGCTTC[C/T]GACTTCGGCTCAGCT | 89848 |
| rs767048524 | snp | C/T | 1.77915e-05 | 0.00298252 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646634 | TGGATCTTGTAGTCA[C/T]GGGCAGCTCGGCTGG | 89848 |
| rs767126877 | in-del | -/G | 0.00165853 | 0.0287491 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642548 | TAGACATTTAAAAAA[-/G]AAAAAAAGTGGGCAT | 89848 |
| rs767128333 | snp | A/G | 3.31505e-05 | 0.00407113 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649311 | GGTTCTCTGTTCCCT[A/G]TTGGGATGCATACAC | 89848 |
| rs767138088 | snp | C/T | 0.000115949 | 0.00761321 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644605 | CAGGGATTGTCACTG[C/T]CTTGGCTGCTCTCTG | 89848 |
| rs767340406 | snp | C/T | 0.000765208 | 0.0195453 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646289 | ATCACATACATTATG[C/T]CATTTAATCTTCCCT | 89848 |
| rs767455940 | snp | A/G | 1.68264e-05 | 0.0029005 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647517 | ACAGCTCACTGACCA[A/G]GGCCTAGAGAGAACC | 89848 |
| rs767528227 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647873 | TAAACAGACAAGATC[C/T]CCTGCACCACCCACT | 89848 |
| rs767554840 | snp | A/G | 1.66538e-05 | 0.00288559 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641703 | GCAAGGGCCCTTACC[A/G]GCCTGAGTCGAGGTG | 89848 |
| rs767640390 | snp | C/T | 0.000110954 | 0.00744746 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646176 | GCTGCCGCCTCTGCT[C/T]CAGTCGTTGCAGTAC | 89848 |
| rs767678624 | snp | A/G | 1.70898e-05 | 0.00292311 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644447 | AGGAATGCTACAGAG[A/G]CCCAGGAGAGACGGT | 89848 |
| rs767764451 | snp | A/C | 4.95544e-05 | 0.00497742 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640169 | CCTAACCCCTCGTGC[A/C]CTTGAAGGGAACCCC | 89848 |
| rs767880691 | snp | C/G | 1.65605e-05 | 0.0028775 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648950 | CTCATGCCCTCATCC[C/G]TCGAACCTTGGTGCT | 89848 |
| rs767896493 | snp | A/G | 6.87592e-05 | 0.00586301 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648051 | GCAGGTACTCATTGC[A/G]GGCTGCTTGCAGCTG | 89848 |
| rs767926840 | snp | A/G | 1.65649e-05 | 0.00287788 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650427 | GATTGCAGGTCGGGG[A/G]TGAGGTGGGGGATAA | 89848 |
| rs767947758 | snp | A/C/G | 7.05933e-05 | 0.00594074 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648105 | CGGACAGCTAGGAGG[A/C/G]TAAACTGATGTCAAT | 89848 |
| rs767970731 | snp | A/C/T | 4.52727e-05 | 0.00475759 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646097 | CTCACCTGTGCCCGG[A/C/T]GGATGCTCTCTCGCA | 89848 |
| rs768096228 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638911 | AACCTTCTCTTGCCC[C/T]GACCTCCACCTCCAC | 89848 |
| rs768261083 | snp | A/G | | | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640176 | CCTCGTGCACTTGAA[A/G]GGAACCCCAGAGCTT | 89848 |
| rs768292828 | snp | A/G | 1.73324e-05 | 0.00294379 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644307 | CAACACGGCCCCCAA[A/G]TTCTCCCCTCCAGAA | 89848 |
| rs768365874 | snp | C/T | 6.24421e-05 | 0.00558723 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647367 | GGTAAAAAGGATCCC[C/T]GGGGAAGCTCTTAGA | 89848 |
| rs768369208 | in-del | -/AACTATCTTTCCTCCTGGACTG | 1.66592e-05 | 0.00288605 | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639588 | TTGTCCGTCAGGGAC[-/AACTATCTTTCCTCCTGGACTG]GCTCCAAGGAAGGAA | 89848 |
| rs768378070 | snp | A/G | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650398 | TGCCCTCTGCTTGCT[A/G]TAGGATCTGCGGAGA | 89848 |
| rs768380573 | snp | C/T | 1.67953e-05 | 0.00289782 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644404 | CTCCTCTGCACTCTG[C/T]CCGGTGTAGCTGTAC | 89848 |
| rs768452937 | snp | C/T | 3.3129e-05 | 0.00406982 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648914 | CACTAGACTACTCTG[C/T]CTCCCTCTTCCCTGC | 89848 |
| rs768468119 | snp | A/C | 1.67253e-05 | 0.00289178 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650996 | ACGAAGGTGAGTGTA[A/C]ATGAAGGGGGTTGGG | 89848 |
| rs768517609 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638843 | AGAGGATTGTTCGCT[C/G]CATCATCCAGAATGA | 89848 |
| rs768524300 | snp | C/G/T | 8.60554e-05 | 0.00655905 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648050 | AGCAGGTACTCATTG[C/G/T]GGGCTGCTTGCAGCT | 89848 |
| rs768542887 | snp | A/G | 2.64645e-05 | 0.00363752 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646076 | TCTCTAACCTCAGGG[A/G]TGTGCCTCACCTGTG | 89848 |
| rs768614134 | snp | C/G | 3.98525e-05 | 0.00446371 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645865 | ATGGCTGGCTTCAGC[C/G]AGCGCTCCACATCTA | 89848 |
| rs768621542 | snp | C/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651824 | CTGACGAAGAGAGGG[C/G]TGGTCCCAGACCTTT | 89848 |
| rs768710494 | snp | C/T | 3.31362e-05 | 0.00407026 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644672 | GGACAAAGCCTACCT[C/T]GCCGTGCTGGTTCCG | 89848 |
| rs768802618 | snp | C/G | 1.6477e-05 | 0.00287024 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640399 | CATTGTTGACCCCTC[C/G]CCTTTCTCTCAGGTG | 89848 |
| rs768950230 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650681 | AGGTGAAGACTGATG[G/T]GGGCCTGGGTACGAT | 89848 |
| rs769018125 | snp | A/G | 1.82931e-05 | 0.00302427 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645161 | AGCCTAGAGGGGCAA[A/G]GAACAGACCTCATAT | 89848 |
| rs769029026 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643326 | GTACCAATTCATTCA[A/G]TCCTCACCACTACCC | 89848 |
| rs769123664 | snp | C/T | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649463 | GGTATCGGTCAGACG[C/T]CTGGAGTCGGGTTTG | 89848 |
| rs769138429 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649672 | TGGGAGCCCATCAAT[C/T]GATCAGCCCATTAGC | 89848 |
| rs769168850 | in-del | -/C | 1.66207e-05 | 0.00288272 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649141 | CTCCCTGTTCCCCAA[-/C]CTTGGGCTTCCTCAC | 89848 |
| rs769217695 | snp | C/G | 2.00971e-05 | 0.00316988 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647388 | AGCTCTTAGAGGCCA[C/G]AGCCCTCACCTGGGA | 89848 |
| rs769257857 | snp | C/G | 1.69447e-05 | 0.00291068 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639616 | GAAAAAGCCGCCCCC[C/G]GACAGGGGAGACCAC | 89848 |
| rs769298620 | snp | A/C/T | 3.29962e-05 | 0.00406165 | intron-variant, utr-variant-3-prime, synonymous-codon, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640311 | GTAGGAAAACACAGC[A/C/T]GGGACTGCACTGGGC | 89848 |
| rs769340798 | snp | G/T | 1.65748e-05 | 0.00287874 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649284 | GCAGCACCTCAGCCT[G/T]CGCCCTCTGGAGGTT | 89848 |
| rs769344653 | snp | C/T | 2.20583e-05 | 0.00332094 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646595 | ACACCTGTGCCCCCC[C/T]ACCTCACCCGATGCC | 89848 |
| rs769397167 | snp | C/T | 0.000112721 | 0.0075065 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647880 | ACAAGATCCCCTGCA[C/T]CACCCACTGTCATGG | 89848 |
| rs769418606 | snp | A/G | 1.65291e-05 | 0.00287476 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640150 | GAGGACTCAGGGACA[A/G]CAGCCTAACCCCTCG | 89848 |
| rs769500107 | snp | A/C | 1.65029e-05 | 0.00287248 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640221 | CTGAGGGCCGGAGGG[A/C]GGGGCCCAAGCCCAG | 89848 |
| rs769500524 | snp | A/G | 7.04151e-05 | 0.00593318 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645063 | CAGGGGAGGGCCCTC[A/G]TGGCCAGGGCTTGGG | 89848 |
| rs769631846 | snp | C/G | 7.18451e-05 | 0.00599311 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646089 | GGGTGTGCCTCACCT[C/G]TGCCCGGCGGATGCT | 89848 |
| rs769655368 | snp | A/C | 6.73049e-05 | 0.00580068 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644412 | CACTCTGTCCGGTGT[A/C]GCTGTACAGGGCCTG | 89848 |
| rs769776835 | snp | G/T | 6.64397e-05 | 0.00576328 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649492 | TGGCCCCCAGCCACG[G/T]TGGCATCCAGCAGGC | 89848 |
| rs769850373 | in-del | -/ACTC | 3.49455e-05 | 0.00417989 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647850 | ATGTATGTATCATCT[-/ACTC]ACTCTAAACAGACAA | 89848 |
| rs769970706 | snp | A/G | 7.12581e-05 | 0.00596858 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651010 | AAATGAAGGGGGTTG[A/G]GGGAGCTACCTGATG | 89848 |
| rs770010813 | snp | A/G | 1.88379e-05 | 0.00306897 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644819 | GAAGTCCCTCCTACT[A/G]CCCCCAACCCAAGGT | 89848 |
| rs770029074 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642630 | TGCATATTGGGAGGA[C/T]ACCGTGAGAGAAGTT | 89848 |
| rs770044832 | snp | A/C | 1.67178e-05 | 0.00289113 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643061 | GTGCAGGTGGGGAGA[A/C]GCTGGGAGGAGAAGG | 89848 |
| rs770046418 | snp | C/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652094 | TCTTTGGCTCAGGCA[C/T]CTGTCCCAGTACCCC | 89848 |
| rs770084242 | snp | G/T | 3.3151e-05 | 0.00407117 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649297 | CTGCGCCCTCTGGAG[G/T]TTCTCTGTTCCCTAT | 89848 |
| rs770105525 | snp | C/T | 0.000592696 | 0.0172046 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644896 | CCCTCCTCTATGACC[C/T]CCAGCCACTCACCCT | 89848 |
| rs770128553 | snp | C/G | 1.91635e-05 | 0.00309538 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639673 | GGTGCTCCAGGGAAA[C/G]GGGGGCTGAGGTAGG | 89848 |
| rs770181535 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645636 | ATGCAAAGAATGATA[C/T]ATGATGATTTCACTT | 89848 |
| rs770191234 | in-del | -/T | 4.99347e-05 | 0.00499648 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644724 | GAACAGATATTAGAC[-/T]TACCTCAGCAGTCCA | 89848 |
| rs770350102 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647849 | CATGTATGTATCATC[C/T]ACTCACTCTAAACAG | 89848 |
| rs770492101 | snp | C/T | 3.80076e-05 | 0.00435917 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647132 | CAAGCAGGAAGATCT[C/T]ACCTGATCAGTCCCT | 89848 |
| rs770533865 | snp | C/T | 1.65564e-05 | 0.00287714 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645832 | CGCTCCTGCTCCACC[C/T]CATCCTGGGCCTGGG | 89848 |
| rs770571608 | snp | C/T | 9.70827e-05 | 0.00696648 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647888 | CCCTGCACCACCCAC[C/T]GTCATGGGGATCAAG | 89848 |
| rs770598180 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647031 | GAAACCCCCTCTCCA[C/T]GGTGTACACTCACTA | 89848 |
| rs770653110 | snp | A/G | 0.00689897 | 0.0583257 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642548 | TAGACATTTAAAAAA[A/G]AAAAAAAGTGGGCAT | 89848 |
| rs770729469 | snp | A/G | 1.68997e-05 | 0.00290682 | stop-gained, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644427 | AGCTGTACAGGGCCT[A/G]TGCCAGGAATGCTAC | 89848 |
| rs770729724 | snp | G/T | 5.79761e-05 | 0.00538374 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646571 | TGCTGAGACAAGAAG[G/T]TGCACATGACACCTG | 89848 |
| rs770759490 | snp | A/G | 8.50069e-05 | 0.00651891 | stop-gained, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646110 | GGCGGATGCTCTCTC[A/G]CACTTCCTGTAACCT | 89848 |
| rs770859414 | snp | C/T | 4.95642e-05 | 0.00497792 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640164 | AGCAGCCTAACCCCT[C/T]GTGCACTTGAAGGGA | 89848 |
| rs770946972 | snp | C/T | 0.000110638 | 0.00743685 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651328 | GCCCGCCAGGAGTCC[C/T]CATTCAGGGCCAAGC | 89848 |
| rs770986191 | snp | C/G | 4.6379e-05 | 0.00481532 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651054 | CCGCCTCCCTCTGCT[C/G]CCAGGTCTGAAGGAT | 89848 |
| rs771026212 | in-del | -/CT | 4.96907e-05 | 0.00498426 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644614 | TCACTGTCTTGGCTG[-/CT]CTCTGGGAGGGAGAG | 89848 |
| rs771036852 | snp | A/T | 1.65611e-05 | 0.00287755 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649024 | CTTCGGTTTAGCCTG[A/T]GCAGATGAGAGAAAG | 89848 |
| rs771050124 | snp | C/T | 7.43605e-05 | 0.00609711 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649908 | TCCATCTCACCGCTC[C/T]GGTGCCCTTCCCTCT | 89848 |
| rs771183821 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642757 | ATTCAATAAGCTAGT[A/C]CCTTTTCCTTACCTC | 89848 |
| rs771194230 | snp | A/G | 1.68613e-05 | 0.00290351 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640027 | AGGACCCAGGGGGTG[A/G]TCAGGGGTCTGGGGG | 89848 |
| rs771211258 | snp | C/T | 3.36474e-05 | 0.00410153 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641665 | TGGTTGGAATAACCC[C/T]TCTACATACAATCTC | 89848 |
| rs771211398 | snp | A/G | 1.68838e-05 | 0.00290544 | synonymous-codon, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141639007 | TGAAGGAGAAGGGAC[A/G]GTGCAGCTGTCCAGG | 89848 |
| rs771293751 | snp | C/G | 6.63075e-05 | 0.00575755 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649454 | CTAGGTCACGGTATC[C/G]GTCAGACGCCTGGAG | 89848 |
| rs771296495 | snp | A/G/T | 3.7031e-05 | 0.00430284 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644831 | ACTGCCCCCAACCCA[A/G/T]GGTCAGAGCCCGGGG | 89848 |
| rs771342296 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648700 | CCACTGTATCCATAA[G/T]GTCTAGAACAGTGCC | 89848 |
| rs771421299 | snp | A/G | 7.21059e-05 | 0.00600398 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647272 | CTCATTCACTGACTC[A/G]CTCTCCAACCCTGTC | 89848 |
| rs771716033 | snp | G/T | 0.000333167 | 0.0129024 | splice-acceptor-variant, intron-variant | FCHSD1 | GRCh38.p7 | 5:141643090 | GGGGACGGCAGCATC[G/T]GGAGGTGGGGTGGGC | 89848 |
| rs771722267 | snp | A/G | 3.19657e-05 | 0.00399773 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645852 | CTGGGCCTGGGTCAT[A/G]GCTGGCTTCAGCCAG | 89848 |
| rs771770212 | snp | C/G | 1.65748e-05 | 0.00287874 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649386 | TTCACCCCAACCTCT[C/G]AGCCATACCTTCCTA | 89848 |
| rs771805856 | snp | C/T | 0.000216752 | 0.0104081 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639974 | CGAACACCGTGATGG[C/T]TCCCCCACAGACAGG | 89848 |
| rs771839658 | snp | C/G | 1.64977e-05 | 0.00287203 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640293 | GACACTTCTGATCAC[C/G]AGGTAGGAAAACACA | 89848 |
| rs771957885 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640386 | ACTCCTGGTCTCTCA[C/T]TGTTGACCCCTCCCC | 89848 |
| rs772032247 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650514 | CGGTTGGGGGGAGCC[A/C]GGTTCCTAGAGTGTA | 89848 |
| rs772107241 | in-del | -/C | 3.36185e-05 | 0.00409977 | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640050 | TCTGGGGGAGGGCAG[-/C]CCAAGGCAGGGATGC | 89848 |
| rs772138472 | snp | C/T | 2.3965e-05 | 0.00346149 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646590 | ACATGACACCTGTGC[C/T]CCCCCACCTCACCCG | 89848 |
| rs772204598 | snp | A/T | 2.17607e-05 | 0.00329846 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645726 | CCTTCCACTGGAGTT[A/T]TTCCCTTCTAAGTAA | 89848 |
| rs772326688 | snp | C/T | 1.67719e-05 | 0.0028958 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644918 | ACTCACCCTCCGTGA[C/T]TGTCAGCTCATCCTC | 89848 |
| rs772429555 | snp | C/G | 5.13474e-05 | 0.00506666 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647454 | TGACCTCTGCGGCTT[C/G]CAGCTCAGTGTGGCT | 89848 |
| rs772456465 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643719 | CGGGCGTGGCAGCAC[A/G]TGCCTGTAATCCCAG | 89848 |
| rs772519112 | snp | A/G | 3.50238e-05 | 0.00418458 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645055 | GTGCAGGGCAGGGGA[A/G]GGCCCTCGTGGCCAG | 89848 |
| rs772631461 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643081 | GGAGGAGAAGGGGAC[A/G]GCAGCATCTGGAGGT | 89848 |
| rs772634143 | snp | A/G | 1.68889e-05 | 0.00290588 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647482 | GCTCAGGGAGGTCAG[A/G]GGGTCCCTCAAGTGC | 89848 |
| rs772675939 | snp | C/T | 1.68094e-05 | 0.00289904 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641668 | TTGGAATAACCCCTC[C/T]ACATACAATCTCCTC | 89848 |
| rs772677708 | snp | A/G/T | 0.000339706 | 0.0130291 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651362 | CTTTTCGGGGCGGCG[A/G/T]CTGCATCTCCGCTCC | 89848 |
| rs772716969 | snp | A/C | 1.65233e-05 | 0.00287426 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640157 | CAGGGACAGCAGCCT[A/C]ACCCCTCGTGCACTT | 89848 |
| rs772724013 | snp | A/C/G | 3.54555e-05 | 0.00421031 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645076 | TCGTGGCCAGGGCTT[A/C/G]GGGGGCAGGCTCCTC | 89848 |
| rs772725065 | snp | A/G | 1.9162e-05 | 0.00309526 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647408 | CTCACCTGGGAGGTT[A/G]TCTGCTCCCCGCGGT | 89848 |
| rs772766875 | snp | A/C | 0.000117474 | 0.00766312 | utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651380 | GCATCTCCGCTCCAG[A/C]AAGGCGGTCAGCCAC | 89848 |
| rs772782883 | in-del | -/A | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643848 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 89848 |
| rs772799960 | snp | A/C/G/T | 0.000151274 | 0.00869582 | missense, synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649521 | GCAGCGCCAGGCACC[A/C/G/T]AACACTGTCCTGCCC | 89848 |
| rs772920345 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141652907 | TTGAGATGGAGTCTT[A/G]CTCTGTTGCCAGGCT | 89848 |
| rs772949261 | snp | C/T | 2.37826e-05 | 0.0034483 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646090 | GGTGTGCCTCACCTG[C/T]GCCCGGCGGATGCTC | 89848 |
| rs773022132 | snp | G/T | 1.68199e-05 | 0.00289994 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640046 | GGGGTCTGGGGGAGG[G/T]CAGCCCAAGGCAGGG | 89848 |
| rs773142410 | snp | A/G | 1.65636e-05 | 0.00287776 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650416 | GGATCTGCGGAGATT[A/G]CAGGTCGGGGGTGAG | 89848 |
| rs773346518 | in-del | -/CAG | 3.30606e-05 | 0.00406561 | cds-indel | RELL2, FCHSD1 | GRCh38.p7 | 5:141640148 | TGGAGGACTCAGGGA[-/CAG]CAGCCTAACCCCTCG | 89848 |
| rs773363325 | snp | C/T | 0.00037577 | 0.013702 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644820 | AAGTCCCTCCTACTG[C/T]CCCCAACCCAAGGTC | 89848 |
| rs773407413 | snp | A/G | 6.82477e-05 | 0.00584117 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651014 | GAAGGGGGTTGGGGG[A/G]GCTACCTGATGTCCT | 89848 |
| rs773444868 | snp | G/T | 0.000176227 | 0.00938522 | utr-variant-3-prime, downstream-variant-500B, stop-lost | RELL2, FCHSD1 | GRCh38.p7 | 5:141640687 | CTCCTTCATTGTGCT[G/T]ATGGACTACCAGCTG | 89848 |
| rs773450093 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638873 | AAGGTGGGTCTAGCA[C/T]AGCCCCTTGCTCCCT | 89848 |
| rs773503771 | snp | C/G | 0.000114905 | 0.00757888 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639674 | GTGCTCCAGGGAAAG[C/G]GGGGCTGAGGTAGGG | 89848 |
| rs773509569 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641462 | GCTTGAAGATAGGGA[C/G]AGCAGCATCACTGGG | 89848 |
| rs773570572 | snp | A/G | 9.10374e-05 | 0.00674614 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643070 | GGGAGAAGCTGGGAG[A/G]AGAAGGGGACGGCAG | 89848 |
| rs773575052 | snp | C/G | 3.31505e-05 | 0.00407113 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649302 | CCCTCTGGAGGTTCT[C/G]TGTTCCCTATTGGGA | 89848 |
| rs773582412 | snp | C/T | 0.00010599 | 0.007279 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647136 | CAGGAAGATCTCACC[C/T]GATCAGTCCCTGCTG | 89848 |
| rs773662678 | snp | A/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652250 | GTTTTAAATGGCACC[A/G]CATTTCCTCCAGTCA | 89848 |
| rs773662944 | snp | G/T | 3.66421e-05 | 0.00428015 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646732 | ACACACCTGAATGGG[G/T]CAGGGGGTGCTGTGA | 89848 |
| rs773784917 | snp | C/G | 1.83599e-05 | 0.00302979 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645183 | ACCTCATATGGGGCC[C/G]ACTCTCAAGCACTGG | 89848 |
| rs773839285 | snp | A/G | 6.62789e-05 | 0.00575631 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644676 | AAAGCCTACCTCGCC[A/G]TGCTGGTTCCGAGCC | 89848 |
| rs773960097 | snp | A/G | 1.66635e-05 | 0.00288643 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647894 | ACCACCCACTGTCAT[A/G]GGGATCAAGAAGCAG | 89848 |
| rs774155322 | snp | A/C | 1.66203e-05 | 0.00288268 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644553 | CCAGGGTCCTCTAAC[A/C]CAAAATTTCCCTTTC | 89848 |
| rs774170369 | snp | C/T | 8.44898e-05 | 0.00649906 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646118 | CTCTCTCGCACTTCC[C/T]GTAACCTCTGTTCTA | 89848 |
| rs774248692 | snp | C/G | 1.65605e-05 | 0.0028775 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648943 | GCCCCCACTCATGCC[C/G]TCATCCCTCGAACCT | 89848 |
| rs774298715 | in-del | -/GGGCAGGTG | 0.000211138 | 0.0102725 | cds-indel, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639643 | CACTGTGTTCTCTGT[-/GGGCAGGTG]GGGCAGGTGGGGCAG | 89848 |
| rs774311343 | snp | C/G | 1.64904e-05 | 0.00287139 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640270 | CAAATGGGCAGCCAA[C/G]CAAACCAGACACTTC | 89848 |
| rs774356587 | snp | A/G | 1.71126e-05 | 0.00292506 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649545 | CCTGCCCCTCCCCAG[A/G]GAAGGTCTGTGTTGA | 89848 |
| rs774442186 | snp | C/G | 0.000222173 | 0.0105374 | splice-donor-variant | FCHSD1 | GRCh38.p7 | 5:141651347 | TCAGGGCCAAGCTCA[C/G]TTTTCGGGGCGGCGG | 89848 |
| rs774457692 | snp | A/G/T | 6.87803e-05 | 0.00586397 | missense, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646095 | GCCTCACCTGTGCCC[A/G/T]GCGGATGCTCTCTCG | 89848 |
| rs774514082 | snp | A/G | 8.53789e-05 | 0.00653316 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641541 | TCCGGGGCTTTAGCC[A/G]GCGGGGGAGGTGGTG | 89848 |
| rs774529589 | snp | A/G | 1.65608e-05 | 0.00287752 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649029 | GTTTAGCCTGTGCAG[A/G]TGAGAGAAAGGAGTC | 89848 |
| rs774547067 | snp | A/G | 2.53849e-05 | 0.00356256 | missense, synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646167 | CTGAAGCCTGCTGCC[A/G]CCTCTGCTCCAGTCG | 89848 |
| rs774602082 | snp | A/G | 1.69458e-05 | 0.00291078 | synonymous-codon, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141639010 | AGGAGAAGGGACAGT[A/G]CAGCTGTCCAGGTGA | 89848 |
| rs774725894 | snp | A/G | 4.46239e-05 | 0.00472334 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651065 | TGCTGCCAGGTCTGA[A/G]GGATGCTCAGCTGTT | 89848 |
| rs774737987 | snp | C/T | 2.87031e-05 | 0.00378823 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647153 | ATCAGTCCCTGCTGG[C/T]TGAAACTGCTGAGGT | 89848 |
| rs774747591 | snp | A/G | 4.1612e-05 | 0.00456117 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647361 | GGGAAGGGTAAAAAG[A/G]ATCCCCGGGGAAGCT | 89848 |
| rs774872418 | snp | A/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652606 | CCAAATAGAATCCAT[A/G]GCCTTCAAGGCTACG | 89848 |
| rs774973573 | snp | A/C | 1.66924e-05 | 0.00288893 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639980 | CCGTGATGGCTCCCC[A/C]ACAGACAGGAGCTGG | 89848 |
| rs774979988 | in-del | -/G | 1.65905e-05 | 0.0028801 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649179 | GACCCCACCTGGCCT[-/G]GACATCAGCCGCCTT | 89848 |
| rs775076023 | snp | C/T | 7.43301e-05 | 0.00609586 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645861 | GGTCATGGCTGGCTT[C/T]AGCCAGCGCTCCACA | 89848 |
| rs775079913 | snp | A/G | 3.31285e-05 | 0.00406978 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644656 | TTGAGATATCGCTCA[A/G]GGACAAAGCCTACCT | 89848 |
| rs775140214 | snp | C/G | 1.6574e-05 | 0.00287867 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649388 | CACCCCAACCTCTGA[C/G]CCATACCTTCCTAAG | 89848 |
| rs775163811 | snp | A/G | 1.7093e-05 | 0.00292339 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643094 | ACGGCAGCATCTGGA[A/G]GTGGGGTGGGCACAG | 89848 |
| rs775188021 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647588 | AAAATAGGCTCGTTC[C/T]AGATTTGACAGGTGA | 89848 |
| rs775199549 | snp | C/T | 3.29902e-05 | 0.00406128 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640307 | CCAGGTAGGAAAACA[C/T]AGCCGGGACTGCACT | 89848 |
| rs775287532 | snp | C/G | 3.29544e-05 | 0.00405908 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640388 | TCCTGGTCTCTCATT[C/G]TTGACCCCTCCCCTT | 89848 |
| rs775394855 | snp | C/T | 2.89222e-05 | 0.00380267 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646181 | CGCCTCTGCTCCAGT[C/T]GTTGCAGTACCTGGT | 89848 |
| rs775439699 | snp | A/G | | | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646229 | GGGGTGGGTGGAAAT[A/G]CTGTGGGGCATGACT | 89848 |
| rs775482820 | snp | A/G | 6.87132e-05 | 0.00586105 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644453 | GCTACAGAGGCCCAG[A/G]AGAGACGGTGAGAGG | 89848 |
| rs775517901 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649629 | CCAACACCATGGGAG[A/G]CAGAGTGCTTTCCCA | 89848 |
| rs775555068 | snp | C/T | 2.1885e-05 | 0.00330787 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645729 | TCCACTGGAGTTTTT[C/T]CCTTCTAAGTAAGGA | 89848 |
| rs775617205 | snp | C/T | 3.3305e-05 | 0.00408061 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639877 | GAGGGCCAAGCAGCC[C/T]CTGAGTTGTGGTCCT | 89848 |
| rs775689075 | snp | C/G | 2.34233e-05 | 0.00342215 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646591 | CATGACACCTGTGCC[C/G]CCCCACCTCACCCGA | 89848 |
| rs775777190 | in-del | -/CT | 1.88276e-05 | 0.00306813 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644813 | ACAGAGAAGTCCCTC[-/CT]CTACTGCCCCCAACC | 89848 |
| rs775789247 | in-del | -/G | 1.65608e-05 | 0.00287752 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648988 | TGGAGACTGGTCCGA[-/G]AGTGGAAGATCCCAT | 89848 |
| rs775815347 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649085 | GAGATCAGAGTCAGG[C/T]CCAGCTTTGGTGACT | 89848 |
| rs775880422 | snp | C/G/T | 3.51848e-05 | 0.00419421 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645062 | GCAGGGGAGGGCCCT[C/G/T]GTGGCCAGGGCTTGG | 89848 |
| rs775888438 | in-del | -/CT | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640839 | GAGAGGTCACAGCCC[-/CT]CAGTCTCTTCTCCTT | 89848 |
| rs775972982 | snp | G/T | 0.000201894 | 0.0100452 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641548 | CTTTAGCCGGCGGGG[G/T]AGGTGGTGGACGCAT | 89848 |
| rs775999054 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642912 | GATGCCTGAAGGCAC[A/G]GAGAGGACCAGAGCG | 89848 |
| rs776157809 | snp | A/G | 1.65605e-05 | 0.0028775 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649038 | GTGCAGATGAGAGAA[A/G]GGAGTCAGGCCCACC | 89848 |
| rs776160649 | snp | G/T | 0.000102867 | 0.00717099 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647174 | CTGCTGAGGTGGGGT[G/T]GGGGAAAATACACCA | 89848 |
| rs776161088 | snp | A/C/T | 4.97214e-05 | 0.00498585 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649406 | ATACCTTCCTAAGCA[A/C/T]CTGCTCCTTGGCGCT | 89848 |
| rs776211787 | snp | C/T | 1.69421e-05 | 0.00291046 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644325 | CTCCCCTCCAGAAGC[C/T]GTCATCTACTCCATC | 89848 |
| rs776277868 | snp | A/G | 4.1468e-05 | 0.00455327 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647368 | GTAAAAAGGATCCCC[A/G]GGGAAGCTCTTAGAG | 89848 |
| rs776444530 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638845 | AGGATTGTTCGCTGC[A/G]TCATCCAGAATGAAG | 89848 |
| rs776490479 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648656 | TCTTAACCAGACTGT[C/G]AGGGCAGGAACTCCA | 89848 |
| rs776530685 | snp | A/T | 1.65704e-05 | 0.00287836 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644576 | TCCCTTTCTTACCTG[A/T]GGGCTCTGCCCCGCA | 89848 |
| rs776616798 | snp | A/G | 0.000181906 | 0.00953518 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646078 | TCTAACCTCAGGGGT[A/G]TGCCTCACCTGTGCC | 89848 |
| rs776694715 | snp | G/T | 0.000188982 | 0.00971882 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643133 | CTGGCATGTGGGGAG[G/T]TTTTACCAGCTTTTC | 89848 |
| rs776718714 | in-del | -/AGTT | 0.000381435 | 0.0138048 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641579 | CTGTAGGGAACACAC[-/AGTT]AGTGCTCCAGAGTTC | 89848 |
| rs776746563 | snp | G/T | 1.65658e-05 | 0.00287795 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650320 | GGTGATATAAGAGAG[G/T]CTGGAACAAGAGGTA | 89848 |
| rs776808802 | snp | A/G | 5.2228e-05 | 0.00510992 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646693 | ACTCTTGCCAGCCAC[A/G]CCTTCTGCTCCCCAC | 89848 |
| rs776838981 | snp | A/G | 3.31263e-05 | 0.00406965 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650407 | CTTGCTGTAGGATCT[A/G]CGGAGATTGCAGGTC | 89848 |
| rs776861216 | in-del | -/G | 1.65638e-05 | 0.00287778 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644643 | GAGGTCCGGGAAGTT[-/G]AGATATCGCTCAGGG | 89848 |
| rs776910084 | snp | G/T | 3.29533e-05 | 0.00405901 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640412 | TCCCCTTTCTCTCAG[G/T]TGTCTCTACCACAGG | 89848 |
| rs776914243 | snp | A/T | 2.48278e-05 | 0.00352325 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647949 | GCTGAGGGATAGGGG[A/T]GTCTGGGTTAAAACT | 89848 |
| rs776916941 | snp | G/T | 3.35295e-05 | 0.00409434 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641679 | CCTCTACATACAATC[G/T]CCTCCAAGGCAAGGG | 89848 |
| rs777006662 | snp | A/C | 0.000482276 | 0.0155211 | intron-variant, missense | FCHSD1 | GRCh38.p7 | 5:141642482 | TATCCATATGACAAA[A/C]AAGCACATGTACCTC | 89848 |
| rs777023923 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650688 | GACTGATGGGGGCCT[A/G]GGTACGATGTCTGCC | 89848 |
| rs777079548 | snp | A/C | 1.65999e-05 | 0.00288091 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639561 | CATTGCAGCCGCAGC[A/C]AGAGGCCTCCACTTG | 89848 |
| rs777093168 | snp | A/C/T | 3.33969e-05 | 0.00408626 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644539 | ATTTTTCTCCATACC[A/C/T]AGGGTCCTCTAACCC | 89848 |
| rs777179342 | snp | A/G | | | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649467 | TCGGTCAGACGCCTG[A/G]AGTCGGGTTTGGCCC | 89848 |
| rs777199746 | snp | A/G | 1.65773e-05 | 0.00287895 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649218 | CCAAGGCCCACACAC[A/G]TTCCCGCTGCCCATA | 89848 |
| rs777465294 | snp | A/C | 0.000104728 | 0.00723556 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647884 | GATCCCCTGCACCAC[A/C]CACTGTCATGGGGAT | 89848 |
| rs777507316 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650343 | AAGAGGTAAGGTCCA[C/G]AGAAAAGTCCCATAC | 89848 |
| rs777592673 | in-del | -/A | 7.69083e-05 | 0.00620066 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651153 | TGAAGACCCCAGCGC[-/A]AGGACCTAAAAAACA | 89848 |
| rs777646130 | in-del | -/C | 5.12256e-05 | 0.00506065 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647194 | AAAATACACCAGGCT[-/C]CTGAAGAAACAGCTT | 89848 |
| rs777683723 | snp | G/T | 1.90918e-05 | 0.00308959 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651304 | CCCTTAGCTCCCTCC[G/T]TTCCCCCAGCCCGCC | 89848 |
| rs777686666 | snp | C/T | 0.000309023 | 0.0124264 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646306 | ATTTAATCTTCCCTA[C/T]GAGGTGGGTGCTATT | 89848 |
| rs777736671 | snp | C/G | 1.79615e-05 | 0.00299674 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647425 | CTGCTCCCCGCGGTG[C/G]GCATGCTCCAGGATG | 89848 |
| rs777871175 | snp | C/T | 1.90729e-05 | 0.00308805 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651307 | TTAGCTCCCTCCGTT[C/T]CCCCAGCCCGCCAGG | 89848 |
| rs777963028 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643372 | TTTAATAATATGACT[C/T]CTATGTTAGAAGTGA | 89848 |
| rs778041824 | snp | C/T | 3.31549e-05 | 0.0040714 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649373 | AGCCAGCTCTTCCTT[C/T]ACCCCAACCTCTGAG | 89848 |
| rs778319234 | snp | C/G | 1.66974e-05 | 0.00288936 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640098 | CCCCCTGAGAGGCCA[C/G]AGCCCCAGGTCCTAG | 89848 |
| rs778425892 | snp | A/G | 6.59631e-05 | 0.00574258 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640467 | CTGCCTGAGCCCTAA[A/G]TGAGGTAATCTCATC | 89848 |
| rs778527535 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650376 | GCCCATACTCCCGTT[C/T]AATGGCTGCCCTCTG | 89848 |
| rs778606826 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638827 | AATGAGGACACAGTA[A/G]AGAGGATTGTTCGCT | 89848 |
| rs778613820 | snp | A/G | 8.34411e-05 | 0.00645861 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646577 | GACAAGAAGGTGCAC[A/G]TGACACCTGTGCCCC | 89848 |
| rs778615405 | snp | A/G | 1.75674e-05 | 0.00296368 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648031 | ATTGGTAGCCACCAA[A/G]TTAAGCAGGTACTCA | 89848 |
| rs778617505 | snp | G/T | 1.6566e-05 | 0.00287797 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650438 | GGGGGTGAGGTGGGG[G/T]ATAAGGTTATGTTTG | 89848 |
| rs778627027 | snp | C/T | 2.79842e-05 | 0.00374049 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645838 | TGCTCCACCTCATCC[C/T]GGGCCTGGGTCATGG | 89848 |
| rs778650886 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640897 | CCGCCTTCCCCAACA[A/C]CTCGCTCCATATGAT | 89848 |
| rs778704986 | snp | C/T | 0.00019889 | 0.00997022 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649259 | CTTCGGCTCAGCTCC[C/T]GGACAGACTGCAGCA | 89848 |
| rs778707407 | snp | A/C/T | 3.69155e-05 | 0.00429612 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648134 | ATAGGAAGCCCTAGA[A/C/T]CCCCAGAGTCCTTCC | 89848 |
| rs778742907 | snp | C/T | | | | | GRCh38.p7 | 5:141639548 | AGCCCCTTGCCTCCA[C/T]TGCAGCCGCAGCAAG | 89848 |
| rs778751942 | in-del | -/C | 0.00118679 | 0.0243308 | | | GRCh38.p7 | 5:141646588 | CACATGACACCTGTG[-/C]CCCCCCCACCTCACC | 89848 |
| rs778773771 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640365 | TGGGGGGCACTGATA[A/G]GACCTACTCCTGGTC | 89848 |
| rs778792630 | snp | G/T | 0.00122106 | 0.0246787 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646650 | GGGCAGCTCGGCTGG[G/T]CAAGCGCTGAACCTC | 89848 |
| rs778895888 | snp | C/T | 3.49229e-05 | 0.00417854 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647853 | TATGTATCATCTACT[C/T]ACTCTAAACAGACAA | 89848 |
| rs778994415 | snp | C/T | 1.65938e-05 | 0.00288039 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649166 | CCTCACTCTCCATGA[C/T]CCCACCTGGCCTGGA | 89848 |
| rs779155475 | snp | C/G | 1.73945e-05 | 0.00294906 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644482 | GGGAGGTGGGTAGCA[C/G]TGCCCCAGGACCATG | 89848 |
| rs779178806 | snp | A/G | 1.66565e-05 | 0.00288583 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640107 | AGGCCACAGCCCCAG[A/G]TCCTAGCCAGCCCCC | 89848 |
| rs779213216 | snp | G/T | 3.31554e-05 | 0.00407144 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649455 | TAGGTCACGGTATCG[G/T]TCAGACGCCTGGAGT | 89848 |
| rs779301296 | snp | C/T | 3.3264e-05 | 0.0040781 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649500 | AGCCACGGTGGCATC[C/T]AGCAGGCAGCGCCAG | 89848 |
| rs779389441 | snp | A/C | 1.84817e-05 | 0.00303982 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648137 | GGAAGCCCTAGACCC[A/C]CAGAGTCCTTCCAAG | 89848 |
| rs779454867 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640205 | TTCTGCAGAGCCAAC[A/G]CTGAGGGCCGGAGGG | 89848 |
| rs779548115 | snp | C/T | 4.9588e-05 | 0.00497911 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638950 | TCTTTTCCTTCTTCC[C/T]TCAGCCAATGCTGAG | 89848 |
| rs779757616 | snp | C/T | 2.85678e-05 | 0.00377929 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646068 | AGGTGGGATCTCTAA[C/T]CTCAGGGGTGTGCCT | 89848 |
| rs779814544 | in-del | -/GGTGCAG | 7.80671e-05 | 0.00624719 | frameshift-variant, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643015 | CCCCCAGGCAGGACA[-/GGTGCAG]GGGGCCCATCCAACA | 89848 |
| rs779831563 | snp | C/T | 5.74828e-05 | 0.00536079 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647091 | GGCCTAAATCATAAT[C/T]GCCTTTATATGTGGC | 89848 |
| rs779865975 | in-del | -/CAT | 0.000165826 | 0.00910416 | cds-indel | RELL2, FCHSD1 | GRCh38.p7 | 5:141639504 | GACGGAGCCCCCTCC[-/CAT]CATCACACAGTGCAC | 89848 |
| rs779937041 | snp | C/T | 3.30169e-05 | 0.00406293 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640490 | ATCTCATCTTCCCAT[C/T]ACCTACTTAAACTAT | 89848 |
| rs779943843 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650390 | TCAATGGCTGCCCTC[C/T]GCTTGCTGTAGGATC | 89848 |
| rs780026064 | snp | A/C | 0.000152917 | 0.00874271 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643032 | TGCAGGGGGCCCATC[A/C]AACACAGAGGTAGGT | 89848 |
| rs780059109 | snp | C/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651510 | CGCAGGGCGCGGAAG[C/G]GAGAGGGGGCCACCG | 89848 |
| rs780121313 | snp | C/G/T | 3.31819e-05 | 0.00407309 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639945 | ACACACATTGAGAAG[C/G/T]GCTATGGACTGCACG | 89848 |
| rs780125178 | snp | A/G | 1.75121e-05 | 0.00295901 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646673 | TGAACCTCTTTCTCC[A/G]GGCCACTCTTGCCAG | 89848 |
| rs780126795 | snp | A/T | 1.66985e-05 | 0.00288946 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641763 | AGGGCTTTGTCTGGA[A/T]ATAAGAACCACAAGT | 89848 |
| rs780217003 | snp | A/C | 1.68658e-05 | 0.0029039 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639612 | GAAGGAAAAAGCCGC[A/C]CCCGGACAGGGGAGA | 89848 |
| rs780236994 | snp | A/C | 9.82849e-05 | 0.00700948 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649845 | GGCTGAGCTCCCCAT[A/C]ACTTTTTGGCCTCTG | 89848 |
| rs780318195 | snp | C/T | 6.62976e-05 | 0.00575712 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649263 | GGCTCAGCTCCCGGA[C/T]AGACTGCAGCACCTC | 89848 |
| rs780376803 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645617 | GGACTCTATGCCAGA[A/G]ATTATGCAAAGAATG | 89848 |
| rs780405921 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649332 | ATGCATACACAAAGT[C/T]CTTACCTAGACCACC | 89848 |
| rs780446152 | snp | A/C | 0.000135217 | 0.00822134 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647862 | TCTACTCACTCTAAA[A/C]AGACAAGATCCCCTG | 89848 |
| rs780531960 | snp | C/G | 1.82214e-05 | 0.00301834 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645143 | AGAAAGCTCAGCATC[C/G]TCAGCCTAGAGGGGC | 89848 |
| rs780774654 | snp | C/G | 3.6708e-05 | 0.004284 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646255 | TGACTTACTATGGGA[C/G]TGGTACTTTGCTAGT | 89848 |
| rs780914093 | snp | A/G | 1.66366e-05 | 0.0028841 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651006 | GTGTAAATGAAGGGG[A/G]TTGGGGGAGCTACCT | 89848 |
| rs780946903 | snp | A/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650218 | GTCACATGGCTATAA[A/T]TACACAGCAGGGATC | 89848 |
| rs780957776 | snp | A/T | 1.67399e-05 | 0.00289304 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644524 | CTACAACCCCTAACA[A/T]TTTTTCTCCATACCC | 89848 |
| rs780963876 | snp | A/G | 1.65509e-05 | 0.00287666 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640135 | CCCCAGTACAGAATG[A/G]AGGACTCAGGGACAG | 89848 |
| rs780978587 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648993 | ACTGGTCCGAGAGTG[A/G]AAGATCCCATGGTCA | 89848 |
| rs781056296 | snp | G/T | 1.67725e-05 | 0.00289585 | splice-acceptor-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639463 | CCTCCCTGCTGTCCA[G/T]TGTGGATGCCACCTC | 89848 |
| rs781067300 | snp | A/G | 5.36927e-05 | 0.00518107 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641523 | GGATCTGGGTGGCCA[A/G]GATCCGGGGCTTTAG | 89848 |
| rs781072365 | snp | A/C | 0.000118508 | 0.00769677 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644893 | TCTCCCTCCTCTATG[A/C]CCTCCAGCCACTCAC | 89848 |
| rs781077266 | snp | A/G | 8.28068e-05 | 0.00643402 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648928 | GCCTCCCTCTTCCCT[A/G]CCCCCACTCATGCCC | 89848 |
| rs781197892 | in-del | -/ACTG | 3.36717e-05 | 0.00410302 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647540 | AGAGAACCCCAAGAT[-/ACTG]ACACCACCCTTCCCC | 89848 |
| rs781250282 | snp | G/T | 1.68391e-05 | 0.0029016 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640009 | GGGGCTCTGGTGGGG[G/T]ACAGGACCCAGGGGG | 89848 |
| rs781263173 | snp | C/T | 0.000338626 | 0.0130076 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644811 | GCCACAGAGAAGTCC[C/T]TCCTACTGCCCCCAA | 89848 |
| rs781291502 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649349 | TTACCTAGACCACCT[C/T]TGGTCCCAAGCCAGC | 89848 |
| rs781468564 | snp | C/T | 1.65778e-05 | 0.002879 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647114 | TATGTGGCCTGGTTC[C/T]AACAAGCAGGAAGAT | 89848 |
| rs781472296 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646730 | ACACACACCTGAATG[C/G]GTCAGGGGGTGCTGT | 89848 |
| rs781486940 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653289 | GTTCCCCTCCACAAC[A/G]GAGGATTCATAAGAG | 89848 |
| rs781491352 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641068 | CTCAGACCATTACAG[C/T]TGCTTCGCATCCTGG | 89848 |
| rs781549146 | snp | G/T | 1.82958e-05 | 0.00302449 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645162 | GCCTAGAGGGGCAAA[G/T]AACAGACCTCATATG | 89848 |
| rs781558485 | snp | A/C | 8.55786e-05 | 0.00654079 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647229 | TCTTGCTCCCAGCTT[A/C]CCTAGGGGTTGGGAA | 89848 |
| rs781644990 | snp | C/T | 8.21524e-05 | 0.00640854 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643049 | ACACAGAGGTAGGTG[C/T]AGGTGGGGAGAAGCT | 89848 |
| rs781678272 | snp | C/T | 2.44633e-05 | 0.00349729 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645814 | CGAGCCTCACTGAGC[C/T]GCCGCTCCTGCTCCA | 89848 |
| rs781705723 | snp | A/C/G | 7.79393e-05 | 0.00624208 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645928 | GCCCCCTTCACCTGG[A/C/G]TCACCTGCCATGGGG | 89848 |
| rs781709441 | snp | C/G | 0.00010174 | 0.00713159 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644226 | GCCTCACCTGTTCAG[C/G]GTCAGAGAGTTCAGG | 89848 |
| rs796510038 | in-del | -/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643863 | CAAAAAAAAAAAAAA[-/G]AAGAAGGCTTTACCT | 89848 |