| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs14251 | snp | A/C | 0.483305 | 0.089826 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639543 | TCTGCAGCCCCTTGC[A/C]TCCATTGCAGCCGCA | 89848 |
| rs32955 | snp | C/T | 0.254105 | 0.249966 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639746 | CTCTTTCCTCCTGGA[C/T]TGGGAGCTCCGGCAG | 89848 |
| rs32956 | snp | C/G | 0.228529 | 0.249076 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640314 | GGAAAACACAGCCGG[C/G]ACTGCACTGGGCTGG | 89848 |
| rs32957 | snp | A/G | 0.164387 | 0.234884 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641529 | GGGTGGCCAGGATCC[A/G]GGGCTTTAGCCGGCG | 89848 |
| rs41098 | snp | A/C | 0.33303 | 0.235809 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640533 | GCTCCCTGAACCCCC[A/C]GAGTAAACTGCAGGC | 89848 |
| rs173683 | snp | C/G | 0.494557 | 0.0518841 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648480 | catttcttctctctg[C/G]aatgttcttccccta | 89848 |
| rs187515 | snp | C/T | 0.261056 | 0.249755 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641198 | GAGGTGGGCCAGAAC[C/T]ACTAGAGACCTTGAT | 89848 |
| rs251041 | snp | C/G | 0.438105 | 0.164671 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648321 | taccatggtccacca[C/G]gttcaatatgagctg | 89848 |
| rs251177 | snp | C/T | 0.320335 | 0.239902 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647317 | GAAGAAAAAGGACAA[C/T]GTGTGAAGCAAAGAG | 89848 |
| rs251180 | snp | A/G | 0.261608 | 0.24973 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642368 | ggcaaaggtaggagt[A/G]gaggcaggggcgagg | 89848 |
| rs374073 | snp | A/G | 0.309648 | 0.24278 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643863 | aaaaaaaaaaaaaaa[A/G]aagaaGgctttacct | 89848 |
| rs456998 | snp | G/T | 0.498813 | 0.0243321 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645595 | GCTCATAATAAAAAT[G/T]TACTGAGGACTCTAT | 89848 |
| rs467478 | snp | A/G | 0.29175 | 0.246489 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644166 | GGCTTCATTGGGGTG[A/G]GAGGGTCAACCCAGA | 89848 |
| rs467677 | snp | A/G | 0.263535 | 0.249633 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643714 | ttagccgggcgtggc[A/G]gcacgtgcctgtaat | 89848 |
| rs468222 | snp | C/G | 0.367297 | 0.220775 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647833 | GAGCAGAACCAGAGT[C/G]CATGTATGTATCATC | 89848 |
| rs468650 | snp | C/T | 0.261608 | 0.24973 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643315 | gcacttcacgtgtac[C/T]aattcattcaatcct | 89848 |
| rs468920 | snp | C/T | 0.295088 | 0.245901 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644156 | ATGAATATGAGGCTT[C/T]ATTGGGGTGAGAGGG | 89848 |
| rs468968 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647832 | GGAGCAGAACCAGAG[C/T]GCATGTATGTATCAT | 89848 |
| rs469074 | snp | G/T | 0.329684 | 0.23697 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644569 | CAAAATTTCCCTTTC[G/T]TACCTGTGGGCTCTG | 89848 |
| rs469522 | snp | A/G | 0.407538 | 0.194118 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644481 | AGGGAGGTGGGTAGC[A/G]GTGCCCCAGGACCAT | 89848 |
| rs702379 | snp | C/T | 0.329783 | 0.236927 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643281 | cgcttatgtttacta[C/T]gtctcaagtgttctg | 89848 |
| rs702380 | snp | A/C/G | 0.324643 | 0.263409 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642977 | TCTGTTAGCCTCCCA[A/C/G]GGCTCCCAGTTCCTT | 89848 |
| rs1048452 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641194 | AGGTCTCTAGTAGTT[C/T]TGGCCCACCTCTTTC | 89848 |
| rs1048453 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641175 | CCCACCTCTTTCCCC[A/C]CCCTGGCTCCATGAC | 89848 |
| rs1048455 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641157 | CTGGCTCCATGACCC[A/C]CCCCACTCTGGATGC | 89848 |
| rs1048456 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641152 | TCCATGACCCACCCC[A/C]CTCTGGATGCCAGGG | 89848 |
| rs1160948 | in-del | -/AGT | 0.327568 | 0.237662 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641286 | AGAAGAGAAGGTAGT[-/AGT]TCCGGTCCTAGAGAT | 89848 |
| rs2052455 | snp | C/T | 0.322483 | 0.239262 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646014 | TACTCCTCTTTCTGA[C/T]GGTGGGAGGAAGGAA | 89848 |
| rs2291110 | snp | A/C | 0.000960249 | 0.0218907 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644626 | ACTTCCCGGACCTCT[A/C]CCTCCCAGAGAGCAG | 89848 |
| rs2306341 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651453 | CAGAGGGCGGGGCCT[G/T]ACCTGGCCTGGGGCG | 89848 |
| rs3749760 | snp | A/C | 0.0373966 | 0.131529 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646615 | CTACAAGATCCAGAA[A/C]CATGGGCATCGGGTG | 89848 |
| rs3763121 | snp | C/T | 0.462489 | 0.131713 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647895 | CCTGCTTCTTGATCC[C/T]CATGACAGTGGGTGG | 89848 |
| rs3830219 | in-del | -/A | 0.264632 | 0.249571 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649611 | CCCATGGTGTTGGTC[-/A]GGGGGCAGGGGGTGG | 89848 |
| rs3833652 | in-del | -/TAC | 0.336017 | 0.234736 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641281 | TAGGACCGGAACTAC[-/TAC]CTTCTCTTCTGTCAT | 89848 |
| rs3834836 | in-del | -/TTATT | 0.0473654 | 0.146421 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642515 | TATAGCAGTTTTATT[-/TTATT]ATTTATTTTAGATTC | 89848 |
| rs4042097 | in-del | -/GTA | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641284 | ACAGAAGAGAAGGTA[-/GTA]GTTCCGGTCCTAGAG | 89848 |
| rs4912764 | snp | A/C/G | 9.9935e-05 | 0.00706806 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647886 | TCCCCTGCACCACCC[A/C/G]CTGTCATGGGGATCA | 89848 |
| rs6580193 | snp | A/T | 0.0310518 | 0.120672 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642149 | CAGAAAGTTTTAGAA[A/T]AGGCAGGCATTCcac | 89848 |
| rs6863184 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649779 | GTCAGCTCTACCTAC[A/G]GCTCACGTGCCTTCC | 89848 |
| rs6881321 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649691 | CAGCCCATTAGCTCA[A/G]CCACAAGCCTCACTC | 89848 |
| rs6882352 | snp | A/C | 0.00837292 | 0.0641588 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649552 | CTCCCCAGAGAAGGT[A/C]TGTGTTGAGGAGGAG | 89848 |
| rs7711960 | snp | A/G | 0.40853 | 0.193309 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646362 | AATTGAAGTCCAGAG[A/G]GGTTAAGTCACTCCC | 89848 |
| rs7720458 | snp | A/G | 0.442926 | 0.158996 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653036 | cgtgccaccacaacc[A/G]gctaattttgtattt | 89848 |
| rs7720485 | snp | A/G | 0.498415 | 0.0281103 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653094 | tgccaggatggtctc[A/G]aactcctgacctcag | 89848 |
| rs7735382 | snp | C/T | 0.01456 | 0.0840715 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647852 | GTATGTATCATCTAC[C/T]CACTCTAAACAGACA | 89848 |
| rs10059833 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651987 | AGAGCTGGGAGATGC[A/G]CAGGAAGCCCCTGCC | 89848 |
| rs10593116 | in-del | -/GA | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642548 | TAGACATTTAAAAAA[-/GA]AAAAAAGTGGGCATC | 89848 |
| rs10699129 | in-del | -/GGGG | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643219 | ATGCTTGCATTCGGT[-/GGGG]GGGGGGGTGTAGCTG | 89848 |
| rs11167754 | snp | A/G | 0.312593 | 0.242037 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646527 | ATGACACCCTCAATG[A/G]CTCCAAGATCCCCTC | 89848 |
| rs11739451 | snp | A/G | 0.238666 | 0.249743 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649505 | CGGTGGCATCCAGCA[A/G]GCAGCGCCAGGCACC | 89848 |
| rs11741647 | snp | C/G | 0.245074 | 0.249964 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638887 | ATAGCCCCTTGCTCC[C/G]TCTTCTCCAACCTTC | 89848 |
| rs11742646 | snp | C/G | 0.323368 | 0.238992 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640263 | CAAGAGGCAAATGGG[C/G]AGCCAAGCAAACCAG | 89848 |
| rs11948807 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650816 | GTTCCTGTGTGTTTA[A/T]GTGGGTGGGAGGGGG | 89848 |
| rs12659397 | snp | C/T | 0.401392 | 0.198948 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648582 | ccccttgttattctt[C/T]atcatagtaccttgt | 89848 |
| rs12659410 | snp | C/T | 0.101301 | 0.200969 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648644 | gctgtctgtctctct[C/T]aaccagactgtgagg | 89848 |
| rs17097413 | snp | C/T | 0.225597 | 0.248806 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651540 | GAGAAACTAAACCTG[C/T]TACTGCTGCGAATAC | 89848 |
| rs17286989 | snp | A/C | 0.118184 | 0.212425 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647245 | CCTAGGGGTTGGGAA[A/C]AGTCAAAGTCACTCA | 89848 |
| rs17287002 | snp | C/T | 0.154079 | 0.230866 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651073 | GGTCTGAAGGATGCT[C/T]AGCTGTTCCAGGAAG | 89848 |
| rs17855844 | snp | C/G | 0.324369 | 0.238682 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640002 | AGGAGCTGGGGCTCT[C/G]GTGGGGGACAGGACC | 89848 |
| rs17855845 | snp | C/T | 0 | 0 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639528 | ACAGTGCACCTGGGC[C/T]CTGCAGCCCCTTGCC | 89848 |
| rs28370911 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649644 | ACAGAGTGCTTTCCC[A/G]TCCTCCCTTGTCTGG | 89848 |
| rs34422888 | in-del | -/T | | | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639245 | TAGTGCCACTCCTTT[-/T]GGGTTAAGCAGTGTT | 89848 |
| rs34704377 | multinucleotide-polymorphism | CC/TG | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647832 | GGAGCAGAACCAGAG[CC/TG]CATGTATGTATCATC | 89848 |
| rs34932115 | in-del | -/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651646 | TGAGTCAAGACGCCT[-/T]AAGTTCTATTTGTAG | 89848 |
| rs35094060 | in-del | -/A | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642555 | TTAAAAAAGAAAAAA[-/A]GTGGGCATCAGAAAA | 89848 |
| rs35340436 | in-del | -/A | | | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640175 | CCTCGTGCACTTGAA[-/A]GGGAACCCCAGAGCT | 89848 |
| rs35590706 | in-del | -/TAG | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641285 | CAGAAGAGAAGGTAG[-/TAG]TTCCGGTCCTAGAGA | 89848 |
| rs35869174 | in-del | -/A | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643865 | AAAAAAAAAAAAGAA[-/A]GAAGGCTTTACCTCG | 89848 |
| rs36020673 | in-del | -/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643130 | TCCTGGCATGTGGGG[-/G]AGGTTTTACCAGCTT | 89848 |
| rs55691717 | snp | C/T | 0.0152603 | 0.0860075 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649837 | GTTCCTGGGGCTGAG[C/T]TCCCCATCACTTTTT | 89848 |
| rs55741918 | in-del | -/C/CAG | 0.5 | 0 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645325 | TACTAACAGTAATAG[-/C/CAG]AGTTACAGTAATTGA | 89848 |
| rs56017834 | snp | A/G | | | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639683 | GGAAAGGGGGGCTGA[A/G]GTAGGGGGCCCAGTG | 89848 |
| rs56206715 | in-del | -/A | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643849 | CGAAACTCTGTCTCA[-/A]AAAAAAAAAAAAAGA | 89848 |
| rs56411617 | in-del | -/GGGG/GGGGG | 0.5 | 0 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643226 | CATTCGGTGGGGGGG[-/GGGG/GGGGG]TGTAGCTGACAAATA | 89848 |
| rs58908491 | snp | A/G | 0.275999 | 0.248644 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647659 | ATGAGAAAGGCCCTC[A/G]TGTGCAGAGCACTTA | 89848 |
| rs60039240 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649609 | CCCCACCCCCTGCCC[C/G]CTGACCAACACCATG | 89848 |
| rs61753289 | snp | C/T | 0.000422744 | 0.0145325 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646111 | GCGGATGCTCTCTCG[C/T]ACTTCCTGTAACCTC | 89848 |
| rs61753290 | snp | C/T | 0.0253225 | 0.109636 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644430 | TGTACAGGGCCTGTG[C/T]CAGGAATGCTACAGA | 89848 |
| rs67641160 | snp | C/G | 0.225893 | 0.248835 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650886 | CTGGAGAGGCCAGGC[C/G]TAGGGTGAGGGCTGT | 89848 |
| rs71583662 | snp | A/G | 0.5 | 0 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650838 | GGGAGGGGGTTGGGA[A/G]GGGTTAGGTGGGGGA | 89848 |
| rs71585381 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652443 | TTAGACTTCTGGTCT[A/G]ATATCTGATCTCCTT | 89848 |
| rs72792345 | snp | A/G | 0.039522 | 0.134904 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643741 | TAATCCCAGCTACTC[A/G]AGGGGCTGATACAGG | 89848 |
| rs72792348 | snp | C/G | 0.0923359 | 0.194016 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650848 | TGGGAGGGGTTAGGT[C/G]GGGGAGCATTCCTAT | 89848 |
| rs73285814 | snp | A/G | 0.3744 | 0.216852 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639757 | TGGACTGGGAGCTCC[A/G]GCAGAAGTCAGGCTA | 89848 |
| rs73285819 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647577 | ACCTCTACTGTAAAA[C/T]AGGCTCGTTCCAGAT | 89848 |
| rs73285828 | snp | C/G | 0.227074 | 0.248947 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651279 | CGTCTCCTACCACAA[C/G]TCGGATGCCCCCTTA | 89848 |
| rs73794953 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642759 | TCAATAAGCTAGTAC[C/G]TTTTCCTTACCTCAT | 89848 |
| rs73794955 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647658 | CATGAGAAAGGCCCT[C/T]GTGTGCAGAGCACTT | 89848 |
| rs73794956 | snp | A/T | 0.228842 | 0.249103 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648224 | TGCCTGGCACTACAC[A/T]AAAAATGTTGCATAC | 89848 |
| rs73794957 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648774 | AAAGAAGGGTATTCT[C/T]TCCATTTTATAGAAG | 89848 |
| rs73794959 | snp | A/C | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651275 | TTCCCGTCTCCTACC[A/C]CAAGTCGGATGCCCC | 89848 |
| rs74910284 | snp | A/G | 0.112754 | 0.208958 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646200 | GCAGTACCTGGTTGG[A/G]AAGGCAGAGAACAGG | 89848 |
| rs75142511 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641739 | ATGTCCAGGAACCCA[G/T]GGAAGTCCAGGGCTT | 89848 |
| rs75457247 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648174 | TGAGAAGCCAGATCC[A/C]GAATGGATTCTCACA | 89848 |
| rs75513915 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648278 | CTAGTGCCTTCTGCA[C/T]GCATTTAAAATAAAA | 89848 |
| rs75791926 | snp | A/T | 0.0126979 | 0.078662 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645407 | ATTTAATCTTCATAA[A/T]GACCCAGTGTTAATA | 89848 |
| rs76141781 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642927 | GGAGAGGACCAGAGC[A/G]TGACCTGGGAGTCCA | 89848 |
| rs76634428 | snp | C/T | 0.107694 | 0.205546 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652673 | GTACTCTCCTCCCAC[C/T]GTCTGCTCACTGTGC | 89848 |
| rs76846020 | snp | A/G | 0.00413911 | 0.0453037 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648091 | CTGGGCTGACTGGGC[A/G]GACAGCTAGGAGGGT | 89848 |
| rs77115131 | snp | G/T | 0.0637582 | 0.166775 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646163 | CGCTCTGAAGCCTGC[G/T]GCCGCCTCTGCTCCA | 89848 |
| rs78047479 | snp | A/G | 0.0031376 | 0.0394836 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640726 | AGGGGGTGGGTGGGC[A/G]TGAAAGCCCTCCCCT | 89848 |
| rs78820103 | snp | C/T | 0.0644693 | 0.167566 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639707 | CCCAGTGATCAGGCA[C/T]CTGATCCCAAAAGTG | 89848 |
| rs79041629 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643396 | GAAGTGAGACCCAGG[C/T]TAAGCCAGCTGTCCA | 89848 |
| rs79088401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648758 | ATATTAAAGGACTGA[A/G]AAAGAAGGGTATTCT | 89848 |
| rs79169194 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651537 | ACCGAGAAACTAAAC[C/T]TGTTACTGCTGCGAA | 89848 |
| rs79609691 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647805 | TACTGTACAATGCCA[C/T]GCAGCCAGCTAGGAG | 89848 |
| rs79900076 | snp | C/G/T | 0.00425388 | 0.0459227 | missense, synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639986 | TGGCTCCCCCACAGA[C/G/T]AGGAGCTGGGGCTCT | 89848 |
| rs80342160 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643493 | TCTCTTTCTGCTGTA[G/T]GTATATACATTATAA | 89848 |
| rs111256073 | in-del | -/AG | 0.1472 | 0.227886 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642547 | ATAGACATTTAAAAA[-/AG]AAAAAAAGTGGGCAT | 89848 |
| rs111415837 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651858 | TAATTCCCGCTTAAC[G/T]GGAAAAGCCAGCGTG | 89848 |
| rs111929355 | snp | A/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651596 | GGGCGGGGCGGACGC[A/T]GCGTCCGCTGGGCGG | 89848 |
| rs112041057 | snp | C/G | 0.5 | 0 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648373 | TCTTTTCAAGCGCTT[C/G]TTCCCTTGCTCACAG | 89848 |
| rs112390736 | snp | C/T | 0.000960821 | 0.0218972 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649285 | CAGCACCTCAGCCTG[C/T]GCCCTCTGGAGGTTC | 89848 |
| rs112543254 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640718 | GCAGGGCCAGGGGGT[A/G]GGTGGGCGTGAAAGC | 89848 |
| rs112898157 | in-del | -/AGC | 0.358303 | 0.225323 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645323 | AATACTAACAGTAAT[-/AGC]AGAGTTACAGTAATT | 89848 |
| rs112961488 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644130 | AACTGGGGAGCAGAG[G/T]AGGCATTAAGATGAA | 89848 |
| rs113111824 | snp | A/G | 0.000431736 | 0.0146861 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639492 | TCCAGCCTGCAGGAC[A/G]GAGCCCCCTCCCATC | 89848 |
| rs113801354 | snp | C/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652525 | ATCAACCTTTTTTTT[C/G]TTTTTTAAAGGGAAA | 89848 |
| rs113911888 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648457 | CACCTCAGACCCTTT[G/T]CACTCACCATTTCTT | 89848 |
| rs114393517 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643854 | ACTCTGTCTCAAAAA[A/C]AAAAAAAAGAAGAAG | 89848 |
| rs114773384 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641443 | TTGATGGTGTGGTCT[C/G]ACAGCTTGAAGATAG | 89848 |
| rs115056843 | snp | A/G | 0.00308354 | 0.0391441 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647151 | TGATCAGTCCCTGCT[A/G]GCTGAAACTGCTGAG | 89848 |
| rs115108469 | snp | C/G | 0.0197687 | 0.0974348 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651826 | GACGAAGAGAGGGCT[C/G]GTCCCAGACCTTTTC | 89848 |
| rs115301013 | snp | G/T | 0.00358779 | 0.0422022 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653225 | GTTTCTTCACAGCAC[G/T]AAACTCACTTGTTCA | 89848 |
| rs115399557 | snp | A/G | 0.00195403 | 0.0311961 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649328 | TGGGATGCATACACA[A/G]AGTCCTTACCTAGAC | 89848 |
| rs116046686 | snp | C/T | 0.0310518 | 0.120672 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640990 | GGCCCCCTGCCCTCT[C/T]AGCACAAGAGGCCCA | 89848 |
| rs116312669 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650852 | AGGGGTTAGGTGGGG[A/G]AGCATTCCTATCCAG | 89848 |
| rs116479483 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643426 | AAAATCACGAAGCCA[A/G]TTATTGGCAGAGTGC | 89848 |
| rs116486808 | snp | A/C | 0.0244538 | 0.107838 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652277 | GTCAGTTAAGTCAGA[A/C]ACCCAGAGTCAATGT | 89848 |
| rs116632951 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642719 | TGTGTAGTCCACAGG[C/T]ATCTTTTTTAACTCT | 89848 |
| rs116772138 | snp | G/T | 0.0376346 | 0.131913 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641727 | CGAGGTGCCATCATG[G/T]CCAGGAACCCAGGGA | 89848 |
| rs116801073 | snp | A/G | 0.00149167 | 0.0272692 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649469 | GGTCAGACGCCTGGA[A/G]TCGGGTTTGGCCCCC | 89848 |
| rs117127684 | snp | C/T | 0.00278599 | 0.0372188 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640685 | GTCTCCTTCATTGTG[C/T]TGATGGACTACCAGC | 89848 |
| rs117179945 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649140 | CCTCCCTGTTCCCCA[A/G]CCTTGGGCTTCCTCA | 89848 |
| rs117633393 | snp | C/T | 0.00429594 | 0.0461467 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645170 | GGGCAAAGAACAGAC[C/T]TCATATGGGGCCCAC | 89848 |
| rs118093952 | snp | C/T | 0.0114934 | 0.0749307 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643002 | TTCCTTCCACTCACC[C/T]CCAGGCAGGACAGGT | 89848 |
| rs118121205 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646819 | ACCTCCAAGGACAAG[A/G]ACAAAGAGAAAGGGG | 89848 |
| rs138005647 | snp | C/T | 3.31708e-05 | 0.00407238 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639937 | TCCGGGTGACACACA[C/T]TGAGAAGCGCTATGG | 89848 |
| rs138513971 | snp | A/G | 0.00122809 | 0.0247495 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639024 | TGCAGCTGTCCAGGT[A/G]AGCTGGAAACAAGGG | 89848 |
| rs138532178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651179 | AAACACTCCGCGCAG[A/G]GAGCGGTGAGGGGGC | 89848 |
| rs138592206 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645274 | GCACCCATCCACTCA[C/T]CATGTACACAACCAC | 89848 |
| rs138687686 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652623 | CCTTCAAGGCTACGC[A/G]TGGAAGACCCTGCTG | 89848 |
| rs139014914 | snp | A/G | 3.31917e-05 | 0.00407367 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639556 | GCCTCCATTGCAGCC[A/G]CAGCAAGAGGCCTCC | 89848 |
| rs139107539 | in-del | -/TCTCA | 0.030665 | 0.119967 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643149 | TTTACCAGCTTTTCC[-/TCTCA]TCTCATCCCATCTCC | 89848 |
| rs139146106 | snp | A/C/G | 5.05389e-05 | 0.00502666 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640038 | GGTGGTCAGGGGTCT[A/C/G]GGGGAGGGCAGCCCA | 89848 |
| rs139206388 | snp | A/G | 0.000351538 | 0.0132531 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644367 | GCAGCAGACGGATGA[A/G]TGCCCCCTCAGGGAA | 89848 |
| rs139324945 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640601 | GGTAGGGAAGGTCCT[A/G]GAGCCCCAGGGGAAA | 89848 |
| rs139650880 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653288 | TGTTCCCCTCCACAA[C/T]GGAGGATTCATAAGA | 89848 |
| rs139821919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642375 | GTAGGAGTAGAGGCA[A/G]GGGCGAGGGTTGAAA | 89848 |
| rs139825311 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641975 | AAGGGAGATAGGATG[C/T]ATAGTGCTCCCACCC | 89848 |
| rs139840036 | snp | C/T | 0.00018322 | 0.00956957 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639588 | CTTGTCCGTCAGGGA[C/T]GCTCCAAGGAAGGAA | 89848 |
| rs140209804 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643773 | GAATCGTTTGAACCC[A/G]GGAGGCAGAGGTTGC | 89848 |
| rs140243622 | snp | C/T | 0.00111163 | 0.0235496 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639456 | CTCCCCTCCTCCCTG[C/T]TGTCCAGTGTGGATG | 89848 |
| rs140791780 | snp | C/T | 0.00504953 | 0.0499927 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644297 | GGGAAGACCCCAACA[C/T]GGCCCCCAAATTCTC | 89848 |
| rs141454875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646431 | ATTTGAACCTATGTC[A/G]GTCTAGCTCCAAAAA | 89848 |
| rs141623307 | snp | A/C | 1.67517e-05 | 0.00289406 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640065 | CCCAAGGCAGGGATG[A/C]CTGCCATGGAGAGGC | 89848 |
| rs141725643 | snp | A/G | 0.0162398 | 0.0886349 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653358 | ACCTGGCACCAATTA[A/G]GTGCACAATACATAT | 89848 |
| rs143056584 | snp | G/T | 6.62427e-05 | 0.00575473 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649016 | CATGGTCACTTCGGT[G/T]TAGCCTGTGCAGATG | 89848 |
| rs143219441 | snp | C/T | 0.000275639 | 0.0117364 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644459 | GAGGCCCAGGAGAGA[C/T]GGTGAGAGGGAGGTG | 89848 |
| rs143223666 | snp | C/G | 4.96389e-05 | 0.00498166 | missense, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141638967 | CAGCCAATGCTGAGG[C/G]CTTGAAGGAGATGCT | 89848 |
| rs143284170 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641374 | GTTTCCACCCTTGGA[A/G]GTGAGGGTGGAAATA | 89848 |
| rs143379809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646917 | AGGTCAAGGGACAGA[A/G]GTAGAATGAAAAGGA | 89848 |
| rs143447644 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643349 | CACTACCCCATGAGG[A/T]AGGCATTTTTAATAA | 89848 |
| rs143590565 | snp | A/G | 0.000812866 | 0.0201438 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639946 | CACACATTGAGAAGC[A/G]CTATGGACTGCACGA | 89848 |
| rs144069501 | snp | C/T | 1.66164e-05 | 0.00288235 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639573 | AGCAAGAGGCCTCCA[C/T]TTGTCCGTCAGGGAC | 89848 |
| rs144253237 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645583 | TCATTCTATTATGCT[C/T]ATAATAAAAATGTAC | 89848 |
| rs144355880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640532 | GGCTCCCTGAACCCC[A/C]CGAGTAAACTGCAGG | 89848 |
| rs145019533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642838 | TTGGAGATGACAGAG[C/T]GGGACCTGAACCAGT | 89848 |
| rs145194186 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643835 | CCTGGGCAACAAGAG[C/T]GAAACTCTGTCTCAA | 89848 |
| rs145350860 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642023 | ACCAATAATGAAACC[C/T]CAACAAACACAATAA | 89848 |
| rs145547239 | snp | A/G | 6.73809e-05 | 0.00580396 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639610 | AGGAAGGAAAAAGCC[A/G]CCCCCGGACAGGGGA | 89848 |
| rs146298065 | snp | A/C/G/T | 0.000403368 | 0.0141962 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640005 | AGCTGGGGCTCTGGT[A/C/G/T]GGGGACAGGACCCAG | 89848 |
| rs146456008 | snp | A/G | 0.000315943 | 0.0125647 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639580 | GGCCTCCACTTGTCC[A/G]TCAGGGACGCTCCAA | 89848 |
| rs146753497 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647015 | GGTGAGCTGGAGTTC[A/T]GAAACCCCCTCTCCA | 89848 |
| rs146759562 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643539 | ATTGAAACACCTTCT[A/G]CATTCCACTGCACTA | 89848 |
| rs147092968 | snp | A/C | 8.38371e-05 | 0.00647391 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640080 | CCTGCCATGGAGAGG[A/C]TGCCCCCTGAGAGGC | 89848 |
| rs147099286 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650648 | CTCCCCACCCCAGAG[A/G]TTCATCTGTAGGCTT | 89848 |
| rs147101461 | snp | A/C/T | 0.000983348 | 0.0221527 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644730 | ATATTAGACTTACCT[A/C/T]AGCAGTCCATGACCC | 89848 |
| rs147498015 | snp | C/T | 1.73024e-05 | 0.00294124 | synonymous-codon, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141639019 | GACAGTGCAGCTGTC[C/T]AGGTGAGCTGGAAAC | 89848 |
| rs147539548 | snp | G/T | 0.0233149 | 0.105422 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641526 | TCTGGGTGGCCAGGA[G/T]CCGGGGCTTTAGCCG | 89848 |
| rs147798196 | snp | C/T | 0.000182335 | 0.00954643 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649217 | GCCAAGGCCCACACA[C/T]GTTCCCGCTGCCCAT | 89848 |
| rs148592125 | snp | C/G | 3.32502e-05 | 0.00407725 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639488 | CACCTCCAGCCTGCA[C/G]GACGGAGCCCCCTCC | 89848 |
| rs148738642 | snp | C/T | 0.00149067 | 0.0272601 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646166 | TCTGAAGCCTGCTGC[C/T]GCCTCTGCTCCAGTC | 89848 |
| rs148872822 | in-del | -/AGGGAAA/AGGGAGA | 0.00421034 | 0.0456899 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644197 | GTGCCTGGGGAGTTC[-/AGGGAAA/AGGGAGA]AGGGAGAAGGTAAGC | 89848 |
| rs148911284 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639644 | CACTGTGTTCTCTGT[A/G]GGCAGGTGGGGCAGG | 89848 |
| rs149353238 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652719 | GTTCCCTCAGTAGAC[C/G]AAGTCCCTTCCAATG | 89848 |
| rs149611844 | snp | A/T | 1.64768e-05 | 0.00287021 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640363 | TCTGGGGGGCACTGA[A/T]AGGACCTACTCCTGG | 89848 |
| rs149872358 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647583 | ACTGTAAAATAGGCT[C/T]GTTCCAGATTTGACA | 89848 |
| rs149876519 | in-del | -/GTA | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641282 | TGACAGAAGAGAAGG[-/GTA]TAGTTCCGGTCCTAG | 89848 |
| rs149927716 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642638 | GGGAGGACACCGTGA[C/G]AGAAGTTAGCTAATT | 89848 |
| rs150119878 | snp | A/G | 0.0104096 | 0.0713894 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644350 | TCCATCTTGGGCCCG[A/G]GGCAGCAGACGGATG | 89848 |
| rs150277585 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651981 | TCGGCGAGAGCTGGG[A/G]GATGCGCAGGAAGCC | 89848 |
| rs150312997 | snp | C/G | 0.000336338 | 0.0129636 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639607 | CCAAGGAAGGAAAAA[C/G]CCGCCCCCGGACAGG | 89848 |
| rs150640745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642281 | GCATGTTCTCACTTA[C/T]AAGTGGGAGCTAAAC | 89848 |
| rs150727860 | snp | C/T | 0.000530636 | 0.0162799 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639546 | GCAGCCCCTTGCCTC[C/T]ATTGCAGCCGCAGCA | 89848 |
| rs150855436 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646510 | CTCCCCTCTGTAGCT[C/G]CATGACACCCTCAAT | 89848 |
| rs180844101 | snp | A/T | | | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639207 | CTCTCTCATCTAGAT[A/T]TCATCAAGCCTAACA | 89848 |
| rs181346623 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640581 | TCCCTTGGTTTGGTG[G/T]TGGAGGTAGGGAAGG | 89848 |
| rs181718574 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641706 | AGGGCCCTTACCGGC[C/T]TGAGTCGAGGTGCCA | 89848 |
| rs181924978 | snp | C/T | 0.000386384 | 0.013894 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645921 | CCGGGCAGCCCCCTT[C/T]ACCTGGCTCACCTGC | 89848 |
| rs182135521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641895 | AAAATCCATCACTCT[A/G]TCCACTGTCCTCAAC | 89848 |
| rs182954817 | snp | C/T | 1.80582e-05 | 0.00300479 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647423 | GTCTGCTCCCCGCGG[C/T]GGGCATGCTCCAGGA | 89848 |
| rs183035645 | snp | A/C | 0.000342488 | 0.0130815 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647205 | GGCTCCTGAAGAAAC[A/C]GCTTCAGGTCTTGCT | 89848 |
| rs183046467 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643631 | AAGGCAGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 89848 |
| rs183679247 | snp | G/T | 0.00832972 | 0.0639959 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644250 | GTTCAGGTGGCCCTG[G/T]GGGGCCAAGCAGCTC | 89848 |
| rs183917220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639353 | GAAAAAATGGGGCTT[A/G]GGGAAATTGGGGCTT | 89848 |
| rs184631347 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652796 | AGCGTTCCATCTGTC[A/G]CCTCCAACAGCTTCT | 89848 |
| rs184773423 | snp | C/T | 5.01811e-05 | 0.00500879 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644527 | CAACCCCTAACAATT[C/T]TTCTCCATACCCAGG | 89848 |
| rs185168678 | snp | C/T | 9.72432e-05 | 0.00697224 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642959 | GCTTCCTCCTTCTTC[C/T]TGTCTGTTAGCCTCC | 89848 |
| rs185926620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646472 | AACTATTGTGCCACA[C/T]TGTTACCTTAAAATA | 89848 |
| rs185985693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644792 | CCTAGAAGGGTCTAT[A/G]GAGGCCACAGAGAAG | 89848 |
| rs186230756 | snp | C/T | 0.000134614 | 0.00820299 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641793 | TCAGTCTTCAGACTT[C/T]GTTTTGTTCAATGCT | 89848 |
| rs186315539 | snp | A/G/T | 5.48772e-05 | 0.0052379 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647218 | ACAGCTTCAGGTCTT[A/G/T]CTCCCAGCTTACCTA | 89848 |
| rs186830089 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640917 | CTCCATATGATAGAG[C/T]GTGGCAGCTGGGAGC | 89848 |
| rs187589029 | snp | C/G/T | 0.00272219 | 0.0367934 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647927 | GGAGGTCCTCCTTTC[C/G/T]CTCCCTGCTGAGGGA | 89848 |
| rs187830136 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644067 | TTGGTTTCCCTTTTC[C/T]CTGCCCCCCCATAGG | 89848 |
| rs188477551 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643738 | CTGTAATCCCAGCTA[C/T]TCGAGGGGCTGATAC | 89848 |
| rs189224579 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645336 | AATAGAGTTACAGTA[A/C]TTGAGTGCATACTAT | 89848 |
| rs189227297 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644490 | GGTAGCAGTGCCCCA[A/G]GACCATGACACCCCA | 89848 |
| rs189493850 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652882 | CATCTCCACAATCAC[C/T]CTTTTTTTTTTGAGA | 89848 |
| rs189623370 | snp | C/T | 0.0022832 | 0.0337103 | intron-variant, synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641543 | CGGGGCTTTAGCCGG[C/T]GGGGGAGGTGGTGGA | 89848 |
| rs189638154 | snp | A/G | 0.000115307 | 0.00759211 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638840 | TAGAGAGGATTGTTC[A/G]CTGCATCATCCAGAA | 89848 |
| rs190018708 | snp | C/T | 4.97508e-05 | 0.00498728 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644568 | CCAAAATTTCCCTTT[C/T]TTACCTGTGGGCTCT | 89848 |
| rs190379795 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647319 | AGAAAAAGGACAATG[C/T]GTGAAGCAAAGAGGG | 89848 |
| rs190796828 | snp | A/G | 0.00262687 | 0.036146 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646729 | GACACACACCTGAAT[A/G]GGTCAGGGGGTGCTG | 89848 |
| rs191033860 | snp | G/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641847 | GGCATTCTATAAATA[G/T]TTGTTAAATTAATGG | 89848 |
| rs191292661 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643308 | TCTGCTAGCACTTCA[C/T]GTGTACCAATTCATT | 89848 |
| rs191608161 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141641060 | TAAATCCGCTCAGAC[C/G]ATTACAGCTGCTTCG | 89848 |
| rs191782846 | snp | A/T | 0.00914312 | 0.0669923 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653039 | GCCACCACAACCAGC[A/T]AATTTTGTATTTTTA | 89848 |
| rs192293847 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650837 | TGGGAGGGGGTTGGG[A/G]GGGGTTAGGTGGGGG | 89848 |
| rs192400014 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648566 | TCCCTCTAAATTCTA[A/C]CCCCTTGTTATTCTT | 89848 |
| rs192601596 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644091 | CCATAGGAGATGGGA[A/G]GCCCAGGCCACTGTA | 89848 |
| rs192828716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644508 | CCATGACACCCCAGG[A/G]CTACAACCCCTAACA | 89848 |
| rs192896780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643762 | CTGATACAGGAGAAT[C/T]GTTTGAACCCGGGAG | 89848 |
| rs199612014 | snp | C/G | 1.68255e-05 | 0.00290043 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647506 | CAAGTGCTCTGACAG[C/G]TCACTGACCAGGGCC | 89848 |
| rs199646898 | snp | C/T | 0.000497281 | 0.0157605 | splice-acceptor-variant | FCHSD1 | GRCh38.p7 | 5:141644692 | TGCTGGTTCCGAGCC[C/T]GCTCACCCAGCAATG | 89848 |
| rs199675831 | snp | C/G | 0.000117264 | 0.00765625 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640064 | GCCCAAGGCAGGGAT[C/G]CCTGCCATGGAGAGG | 89848 |
| rs199678864 | snp | C/T | 0.000168067 | 0.00916544 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644406 | CCTCTGCACTCTGTC[C/T]GGTGTAGCTGTACAG | 89848 |
| rs199688158 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649611 | CCACCCCCTGCCCCC[C/T]GACCAACACCATGGG | 89848 |
| rs199786252 | snp | A/G/T | 4.94762e-05 | 0.00497354 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640313 | AGGAAAACACAGCCG[A/G/T]GACTGCACTGGGCTG | 89848 |
| rs199910418 | snp | C/T | 8.29414e-05 | 0.00643924 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639924 | TCCCCTCCCAGGTTC[C/T]GGGTGACACACATTG | 89848 |
| rs199923199 | snp | A/G | 0.00150726 | 0.0274109 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649260 | TTCGGCTCAGCTCCC[A/G]GACAGACTGCAGCAC | 89848 |
| rs199960419 | snp | G/T | 0.000760398 | 0.0194839 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643115 | GTGGGCACAGAGTTA[G/T]TCCTGGCATGTGGGG | 89848 |
| rs199983271 | snp | G/T | 5.01752e-05 | 0.0050085 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644989 | CTGTCCCCCACCCTT[G/T]CCCATCAGAGGTCCC | 89848 |
| rs199997694 | snp | A/G | 0.000431235 | 0.0146776 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649190 | GCCTGGACATCAGCC[A/G]CCTTCTCCTGTGCCA | 89848 |
| rs200010370 | snp | C/T | 0.000232589 | 0.0107815 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649496 | CCCCAGCCACGGTGG[C/T]ATCCAGCAGGCAGCG | 89848 |
| rs200109868 | snp | C/T | 0.00023409 | 0.0108162 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649510 | GCATCCAGCAGGCAG[C/T]GCCAGGCACCGAACA | 89848 |
| rs200119620 | snp | C/T | 3.33178e-05 | 0.00408139 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641702 | GGCAAGGGCCCTTAC[C/T]GGCCTGAGTCGAGGT | 89848 |
| rs200124668 | snp | A/G | 0.000416077 | 0.0144175 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641544 | GGGGCTTTAGCCGGC[A/G]GGGGAGGTGGTGGAC | 89848 |
| rs200176870 | snp | A/G/T | 0.00427204 | 0.0460198 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644326 | TCCCCTCCAGAAGCC[A/G/T]TCATCTACTCCATCT | 89848 |
| rs200186565 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650381 | TACTCCCGTTCAATG[C/G]CTGCCCTCTGCTTGC | 89848 |
| rs200210180 | snp | A/G/T | 0.000269621 | 0.0116078 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640035 | GGGGGTGGTCAGGGG[A/G/T]CTGGGGGAGGGCAGC | 89848 |
| rs200320253 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640228 | CCGGAGGGAGGGGCC[C/T]AAGCCCAGGGCTGCC | 89848 |
| rs200376159 | snp | A/G | 0.000323039 | 0.0127049 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647467 | TTCCAGCTCAGTGTG[A/G]CTCAGGGAGGTCAGG | 89848 |
| rs200412858 | snp | C/T | 0.000217197 | 0.0104188 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644982 | GACTTGGCTGTCCCC[C/T]ACCCTTGCCCATCAG | 89848 |
| rs200503843 | snp | A/C | 0.000265053 | 0.011509 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641489 | TGGGGGTCAAGGCTT[A/C]CCTGGCCTTCAGGTG | 89848 |
| rs200692020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638915 | TTCTCTTGCCCTGAC[C/T]TCCACCTCCACTGAC | 89848 |
| rs200855332 | snp | C/G/T | 0.000625804 | 0.017678 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649247 | TACAGCTTCCGACTT[C/G/T]GGCTCAGCTCCCGGA | 89848 |
| rs200865612 | snp | C/G | 0.000770673 | 0.0196149 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649546 | CTGCCCCTCCCCAGA[C/G]AAGGTCTGTGTTGAG | 89848 |
| rs200873530 | snp | A/C | 0.000233899 | 0.0108118 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639983 | TGATGGCTCCCCCAC[A/C]GACAGGAGCTGGGGC | 89848 |
| rs200877938 | snp | A/G | 0.00072568 | 0.0190345 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645818 | CCTCACTGAGCCGCC[A/G]CTCCTGCTCCACCTC | 89848 |
| rs200902720 | snp | C/T | 0.000811466 | 0.0201265 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644667 | CTCAGGGACAAAGCC[C/T]ACCTCGCCGTGCTGG | 89848 |
| rs200914115 | snp | A/G | 0.00019883 | 0.00996873 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644575 | TTCCCTTTCTTACCT[A/G]TGGGCTCTGCCCCGC | 89848 |
| rs200950841 | snp | C/T | 0.000745632 | 0.019294 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649324 | CTATTGGGATGCATA[C/T]ACAAAGTCCTTACCT | 89848 |
| rs200995822 | snp | C/T | 1.65611e-05 | 0.00287755 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650356 | CAGAGAAAAGTCCCA[C/T]ACCTGCCCATACTCC | 89848 |
| rs201011697 | snp | A/G | 1.67978e-05 | 0.00289804 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641671 | GAATAACCCCTCTAC[A/G]TACAATCTCCTCCAA | 89848 |
| rs201219952 | snp | A/G/T | 0.000133497 | 0.00816897 | synonymous-codon, missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639596 | TCAGGGACGCTCCAA[A/G/T]GAAGGAAAAAGCCGC | 89848 |
| rs201272947 | snp | C/T | 0.000687726 | 0.0185308 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648006 | CCTGGTAGTAATGGT[C/T]GAGGTGGGCATTGGT | 89848 |
| rs201297893 | snp | G/T | 0.000234861 | 0.010834 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647169 | TGAAACTGCTGAGGT[G/T]GGGTGGGGGAAAATA | 89848 |
| rs201374942 | snp | C/G | 1.65616e-05 | 0.00287759 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649062 | GCCCACCCCAAGTGG[C/G]AGAATATGAGATCAG | 89848 |
| rs201427504 | snp | C/T | 0.00040119 | 0.0141575 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644304 | CCCCAACACGGCCCC[C/T]AAATTCTCCCCTCCA | 89848 |
| rs201474232 | snp | C/T | 3.32895e-05 | 0.00407966 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644548 | CATACCCAGGGTCCT[C/T]TAACCCAAAATTTCC | 89848 |
| rs201569710 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645028 | TTCATACCTGATAGC[A/G]AAATACCACGTGTGC | 89848 |
| rs201604452 | snp | G/T | | | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650395 | GGCTGCCCTCTGCTT[G/T]CTGTAGGATCTGCGG | 89848 |
| rs201659999 | snp | A/C/T | 0.000795229 | 0.0199244 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649418 | GCACCTGCTCCTTGG[A/C/T]GCTCCGCCCTGTACC | 89848 |
| rs201695149 | in-del | -/GGGT | 0.0115144 | 0.0749975 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643224 | TGCATTCGGTGGGGG[-/GGGT]GGTGTAGCTGACAAA | 89848 |
| rs201722475 | snp | A/C/G | 0.000108102 | 0.00735115 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641459 | ACAGCTTGAAGATAG[A/C/G]GACAGCAGCATCACT | 89848 |
| rs201729092 | snp | A/G | 0.000132479 | 0.00813768 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648953 | ATGCCCTCATCCCTC[A/G]AACCTTGGTGCTCAG | 89848 |
| rs201826457 | snp | A/G | 0.000313038 | 0.0125068 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640428 | TGTCTCTACCACAGG[A/G]AGCAGGGAGTATGTG | 89848 |
| rs201835761 | snp | C/T | 6.69882e-05 | 0.00578702 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644360 | GCCCGGGGCAGCAGA[C/T]GGATGAGTGCCCCCT | 89848 |
| rs201843663 | snp | G/T | 0.000348263 | 0.0131913 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648010 | GTAGTAATGGTCGAG[G/T]TGGGCATTGGTAGCC | 89848 |
| rs201879067 | snp | A/G | 0.000119883 | 0.00774125 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641550 | TTAGCCGGCGGGGGA[A/G]GTGGTGGACGCATCT | 89848 |
| rs201923955 | in-del | -/AAG | 0.00162675 | 0.0284733 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642546 | TATAGACATTTAAAA[-/AAG]AAAAAAAGTGGGCAT | 89848 |
| rs201933906 | snp | A/G | 0.000115935 | 0.00761277 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650335 | GCTGGAACAAGAGGT[A/G]AGGTCCAGAGAAAAG | 89848 |
| rs202034143 | snp | G/T | 0.00168549 | 0.0289811 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651359 | TCACTTTTCGGGGCG[G/T]CGGCTGCATCTCCGC | 89848 |
| rs202048778 | snp | A/G | 0.00051826 | 0.0160892 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649511 | CATCCAGCAGGCAGC[A/G]CCAGGCACCGAACAC | 89848 |
| rs202070935 | snp | A/G | 6.36639e-05 | 0.00564162 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651135 | GTGGGGGCAAAGAGA[A/G]GATGAAGACCCCAGC | 89848 |
| rs202074054 | snp | A/G/T | 0.000186423 | 0.00965292 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646739 | TGAATGGGTCAGGGG[A/G/T]TGCTGTGAGGAGGAC | 89848 |
| rs202083613 | snp | A/G | 0.000395407 | 0.0140551 | synonymous-codon, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640426 | GGTGTCTCTACCACA[A/G]GGAGCAGGGAGTATG | 89848 |
| rs202160756 | snp | A/G | 0.00281191 | 0.0373905 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650413 | GTAGGATCTGCGGAG[A/G]TTGCAGGTCGGGGGT | 89848 |
| rs202171404 | snp | A/G | 0.000303536 | 0.0123157 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644294 | GAGGGGAAGACCCCA[A/G]CACGGCCCCCAAATT | 89848 |
| rs202174311 | snp | A/G | 0.00103041 | 0.0226748 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639960 | CGCTATGGACTGCAC[A/G]AACACCGTGATGGCT | 89848 |
| rs202176294 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640019 | TGGGGGACAGGACCC[A/G]GGGGGTGGTCAGGGG | 89848 |
| rs267600460 | snp | A/G | | | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644279 | TCTTCCACCAGCAGG[A/G]AGGGGAAGACCCCAA | 89848 |
| rs367584740 | snp | C/T | 3.56246e-05 | 0.00422031 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646641 | TGTAGTCACGGGCAG[C/T]TCGGCTGGTCAAGCG | 89848 |
| rs367603306 | snp | A/G | 0.00013254 | 0.00813957 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644673 | GACAAAGCCTACCTC[A/G]CCGTGCTGGTTCCGA | 89848 |
| rs367620461 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant, utr-variant-3-prime, stop-gained | RELL2, FCHSD1 | GRCh38.p7 | 5:141640351 | ATTGCTCTCTACTCT[A/G]GGGGGCACTGATAGG | 89848 |
| rs367794498 | snp | C/T | 5.38556e-05 | 0.00518892 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645104 | CTCAAAGAGCTCTCC[C/T]GTCTCCTCACATTCC | 89848 |
| rs367880828 | snp | C/T | 0.000101097 | 0.00710902 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649973 | GTGAAAAAGCCATCA[C/T]AGAACCAAGTTCCCT | 89848 |
| rs367937902 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643763 | TGATACAGGAGAATC[A/G]TTTGAACCCGGGAGG | 89848 |
| rs368063756 | snp | C/T | 0.000182193 | 0.00954271 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644634 | TGGGAGGGAGAGGTC[C/T]GGGAAGTTGAGATAT | 89848 |
| rs368112224 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638839 | GTAGAGAGGATTGTT[C/T]GCTGCATCATCCAGA | 89848 |
| rs368115473 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141652921 | TGCTCTGTTGCCAGG[C/T]TGGAGTGCAATGGTG | 89848 |
| rs368224251 | snp | A/G | 1.72505e-05 | 0.00293682 | stop-gained, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648078 | GCTGCTGGGAGTACT[A/G]GGCTGACTGGGCGGA | 89848 |
| rs368318178 | snp | A/C/G | 4.26721e-05 | 0.0046189 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645757 | GGATGGGTAGTGTTG[A/C/G]GGGAGGAGCTCACGG | 89848 |
| rs368341462 | snp | G/T | | | intron-variant, stop-gained | FCHSD1 | GRCh38.p7 | 5:141642500 | GCACATGTACCTCCT[G/T]AATCTAAAATAAATA | 89848 |
| rs368350946 | snp | A/G/T | 6.65916e-05 | 0.00576992 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639967 | GACTGCACGAACACC[A/G/T]TGATGGCTCCCCCAC | 89848 |
| rs368418936 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648905 | GTTCCAAACCACTAG[A/C/T]CTACTCTGCCTCCCT | 89848 |
| rs368535465 | snp | A/G | 4.89872e-05 | 0.00494886 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645807 | GGACAGCCGAGCCTC[A/G]CTGAGCCGCCGCTCC | 89848 |
| rs368889750 | snp | A/G/T | 5.7437e-05 | 0.00535872 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641608 | AGTTCTCCCTTAAGG[A/G/T]TATCCCTGTCTATTC | 89848 |
| rs368897773 | snp | A/C/T | 7.34246e-05 | 0.00605869 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647420 | GTTGTCTGCTCCCCG[A/C/T]GGTGGGCATGCTCCA | 89848 |
| rs369105841 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640325 | CCGGGACTGCACTGG[A/G]CTGGGCTCTTATTGC | 89848 |
| rs369252983 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650594 | GGCAGCTGCAACACA[A/G]GAAACCCTCACCTTA | 89848 |
| rs369260580 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644800 | GGTCTATGGAGGCCA[C/T]AGAGAAGTCCCTCCT | 89848 |
| rs369273824 | snp | C/T | 9.96314e-05 | 0.00705732 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649490 | TTTGGCCCCCAGCCA[C/T]GGTGGCATCCAGCAG | 89848 |
| rs369279681 | snp | A/G | 2.18912e-05 | 0.00330834 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646102 | CTGTGCCCGGCGGAT[A/G]CTCTCTCGCACTTCC | 89848 |
| rs369341926 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647282 | GACTCACTCTCCAAC[C/T]CTGTCCCTAGCACTT | 89848 |
| rs369354908 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648189 | AGAATGGATTCTCAC[A/G]TTATTGAGTGCTTAC | 89848 |
| rs369448667 | snp | C/T | 0.000171962 | 0.00927099 | intron-variant, synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641540 | ATCCGGGGCTTTAGC[C/T]GGCGGGGGAGGTGGT | 89848 |
| rs369538415 | snp | C/T | 0.000117285 | 0.00765695 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644384 | GCCCCCTCAGGGAAG[C/T]TCAGCTCCTCTGCAC | 89848 |
| rs369546060 | snp | C/T | 0.000534759 | 0.016343 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645972 | GTGGAACCTGGCTGA[C/T]GGCAGTGTTTACTCT | 89848 |
| rs369642716 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643868 | AAAAAAAAAAGAAGA[A/C]GGCTTTACCTCGATT | 89848 |
| rs369714142 | snp | G/T | 0.000165725 | 0.00910137 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649444 | GTACCCCCTGCTAGG[G/T]CACGGTATCGGTCAG | 89848 |
| rs369722148 | snp | C/T | 1.67514e-05 | 0.00289403 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641681 | TCTACATACAATCTC[C/T]TCCAAGGCAAGGGCC | 89848 |
| rs369747048 | snp | A/T | 1.66438e-05 | 0.00288472 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644725 | AACAGATATTAGACT[A/T]ACCTCAGCAGTCCAT | 89848 |
| rs369892061 | snp | C/T | 3.30186e-05 | 0.00406303 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640192 | GGAACCCCAGAGCTT[C/T]TGCAGAGCCAACACT | 89848 |
| rs369910947 | snp | C/T | 1.68735e-05 | 0.00290456 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640025 | ACAGGACCCAGGGGG[C/T]GGTCAGGGGTCTGGG | 89848 |
| rs369912804 | snp | C/T | 2.11004e-05 | 0.00324804 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646124 | CGCACTTCCTGTAAC[C/T]TCTGTTCTATGCTTG | 89848 |
| rs369917457 | snp | A/G/T | 5.16252e-05 | 0.00508039 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647449 | CAGGATGACCTCTGC[A/G/T]GCTTCCAGCTCAGTG | 89848 |
| rs369955455 | snp | G/T | 0.000231826 | 0.0107638 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648988 | TGGAGACTGGTCCGA[G/T]AGTGGAAGATCCCAT | 89848 |
| rs370032857 | snp | C/G/T | 0.000276763 | 0.0117603 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644220 | AGGTAAGCCTCACCT[C/G/T]TTCAGGGTCAGAGAG | 89848 |
| rs370104075 | snp | A/G | 6.69792e-05 | 0.00578663 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644361 | CCCGGGGCAGCAGAC[A/G]GATGAGTGCCCCCTC | 89848 |
| rs370137791 | snp | A/C/T | 0.000654461 | 0.0180792 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644913 | CAGCCACTCACCCTC[A/C/T]GTGATTGTCAGCTCA | 89848 |
| rs370159358 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647839 | ACCAGAGTGCATGTA[-/TG]TGTATCATCTACTCA | 89848 |
| rs370226917 | snp | C/T | 0.000298255 | 0.0122081 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643080 | GGGAGGAGAAGGGGA[C/T]GGCAGCATCTGGAGG | 89848 |
| rs370251427 | snp | A/G | 6.66433e-05 | 0.00577211 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639589 | TTGTCCGTCAGGGAC[A/G]CTCCAAGGAAGGAAA | 89848 |
| rs370266583 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641399 | GAAATAAGGGCGATT[C/T]CAGCTTTTGGCTGTG | 89848 |
| rs370287330 | snp | A/C/G/T | 4.32603e-05 | 0.00465066 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647964 | TGTCTGGGTTAAAAC[A/C/G/T]GGCCTTGAGCAGAGC | 89848 |
| rs370399564 | snp | A/G/T | 0.000159899 | 0.00894029 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645081 | GCCAGGGCTTGGGGG[A/G/T]CAGGCTCCTCAAAGA | 89848 |
| rs370499604 | snp | A/G | 0.000151358 | 0.00869806 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644407 | CTCTGCACTCTGTCC[A/G]GTGTAGCTGTACAGG | 89848 |
| rs370499796 | snp | C/T | 0.0017735 | 0.0297255 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649189 | GGCCTGGACATCAGC[C/T]GCCTTCTCCTGTGCC | 89848 |
| rs370511249 | snp | A/G | 1.65899e-05 | 0.00288005 | missense, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141638980 | GGCCTTGAAGGAGAT[A/G]CTGGGGGACAGTGAA | 89848 |
| rs370538741 | snp | A/G | 0.000169986 | 0.00921759 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649904 | GCTGTCCATCTCACC[A/G]CTCCGGTGCCCTTCC | 89848 |
| rs370545898 | snp | C/G | 1.68275e-05 | 0.0029006 | splice-acceptor-variant | FCHSD1 | GRCh38.p7 | 5:141647521 | CTCACTGACCAGGGC[C/G]TAGAGAGAACCCCAA | 89848 |
| rs370575433 | snp | C/T | 2.08288e-05 | 0.00322707 | intron-variant, synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646600 | TGTGCCCCCCCACCT[C/T]ACCCGATGCCCATGG | 89848 |
| rs370612818 | snp | A/G | | | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642376 | TAGGAGTAGAGGCAG[A/G]GGCGAGGGTTGAAAA | 89848 |
| rs370627438 | snp | G/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652624 | CTTCAAGGCTACGCA[G/T]GGAAGACCCTGCTGG | 89848 |
| rs370735476 | snp | C/T | 1.6566e-05 | 0.00287797 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644596 | TCTGCCCCGCAGGGA[C/T]TGTCACTGTCTTGGC | 89848 |
| rs370799818 | snp | A/G | 8.62776e-05 | 0.00656745 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645038 | ATAGCGAAATACCAC[A/G]TGTGCAGGGCAGGGG | 89848 |
| rs370915381 | snp | C/T | 3.34253e-05 | 0.00408797 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644955 | TGCCTGGGCCACACA[C/T]GAAGGATTCAGGACT | 89848 |
| rs370921715 | snp | G/T | 0.000285959 | 0.011954 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649588 | TCCACAGCTTCATGA[G/T]ACCACCCCCACCCCC | 89848 |
| rs370956421 | snp | A/T | 2.29071e-05 | 0.00338424 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644237 | TCAGGGTCAGAGAGT[A/T]CAGGTGGCCCTGGGG | 89848 |
| rs370981253 | in-del | -/CT | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643842 | AACAAGAGCGAAACT[-/CT]GTCTCAAAAAAAAAA | 89848 |
| rs371038528 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648615 | TATTTTCATCTTAAT[C/T]TAAGTATTTATTTGC | 89848 |
| rs371091601 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648342 | ATATGAGCTGGCCCC[C/T]GCAATCTCTCTGACC | 89848 |
| rs371149077 | snp | A/G | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649224 | CCCACACACGTTCCC[A/G]CTGCCCATACAGCTT | 89848 |
| rs371297507 | snp | A/G | 0.000231823 | 0.0107637 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648961 | ATCCCTCGAACCTTG[A/G]TGCTCAGTTTCTGGA | 89848 |
| rs371336881 | snp | A/G | 0.000214672 | 0.0103581 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640495 | ATCTTCCCATCACCT[A/G]CTTAAACTATTTAAG | 89848 |
| rs371370577 | snp | C/T | 3.53201e-05 | 0.00420224 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648028 | GGCATTGGTAGCCAC[C/T]AAGTTAAGCAGGTAC | 89848 |
| rs371398052 | snp | A/G | 0.000143642 | 0.00847351 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645105 | TCAAAGAGCTCTCCC[A/G]TCTCCTCACATTCCT | 89848 |
| rs371490309 | snp | C/T | 1.65773e-05 | 0.00287895 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649367 | GTCCCAAGCCAGCTC[C/T]TCCTTCACCCCAACC | 89848 |
| rs371568045 | snp | C/T | 1.65638e-05 | 0.00287778 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644649 | CGGGAAGTTGAGATA[C/T]CGCTCAGGGACAAAG | 89848 |
| rs371593430 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650603 | AACACAGGAAACCCT[C/G]ACCTTACTGCCCCGG | 89848 |
| rs371766051 | snp | C/T | 0.00034772 | 0.013181 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650368 | CCATACCTGCCCATA[C/T]TCCCGTTCAATGGCT | 89848 |
| rs372000867 | snp | A/G | | | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646526 | CATGACACCCTCAAT[A/G]GCTCCAAGATCCCCT | 89848 |
| rs372037737 | snp | A/G | 0.000101114 | 0.00710961 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646588 | GCACATGACACCTGT[A/G]CCCCCCCACCTCACC | 89848 |
| rs372078947 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648872 | ATTCAACCCAGTCTT[C/T]CATACATATGCACCT | 89848 |
| rs372186496 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643766 | TACAGGAGAATCGTT[G/T]GAACCCGGGAGGCAG | 89848 |
| rs372197502 | snp | A/G | 0.000177101 | 0.00940846 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645973 | TGGAACCTGGCTGAC[A/G]GCAGTGTTTACTCTC | 89848 |
| rs372216012 | snp | A/G | 0.000232015 | 0.0107682 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649286 | AGCACCTCAGCCTGC[A/G]CCCTCTGGAGGTTCT | 89848 |
| rs372221131 | snp | A/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645396 | TATATTGTCTCATTT[A/T]ATCTTCATAATGACC | 89848 |
| rs372282382 | snp | A/G | 0.00205719 | 0.0320057 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638872 | GAAGGTGGGTCTAGC[A/G]TAGCCCCTTGCTCCC | 89848 |
| rs372379172 | snp | C/T | 3.31444e-05 | 0.00407076 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649435 | CTCCGCCCTGTACCC[C/T]CTGCTAGGTCACGGT | 89848 |
| rs372439670 | snp | A/G | 6.60175e-05 | 0.00574494 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640215 | CCAACACTGAGGGCC[A/G]GAGGGAGGGGCCCAA | 89848 |
| rs372463543 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645322 | ATAATACTAACAGTA[A/G]TAGAGTTACAGTAAT | 89848 |
| rs372637256 | snp | A/G | 0.000163987 | 0.00905353 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650424 | GGAGATTGCAGGTCG[A/G]GGGTGAGGTGGGGGA | 89848 |
| rs372639731 | snp | C/T | 0.000170747 | 0.00923819 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646109 | CGGCGGATGCTCTCT[C/T]GCACTTCCTGTAACC | 89848 |
| rs372757325 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642203 | TGTCCTCTGCAGCAA[C/T]ATGAATGGAGTTGGA | 89848 |
| rs372761136 | snp | A/C/G | 0.000461225 | 0.0151796 | missense, synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644871 | CACCTTGACCCATTC[A/C/G]TCAGCATCTCCCTCC | 89848 |
| rs372866853 | snp | A/G | 5.29815e-05 | 0.00514665 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646656 | CTCGGCTGGTCAAGC[A/G]CTGAACCTCTTTCTC | 89848 |
| rs372867388 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647774 | GAGGAATCTGGGGTT[C/T]GGAAGAGTTTAAGTG | 89848 |
| rs372901612 | snp | A/C/G | 3.31516e-05 | 0.0040712 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644687 | CGCCGTGCTGGTTCC[A/C/G]AGCCTGCTCACCCAG | 89848 |
| rs372907773 | in-del | -/T | | | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640004 | GAGCTGGGGCTCTGG[-/T]GGGGGACAGGACCCA | 89848 |
| rs372908608 | snp | G/T | | | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649953 | GCCAGTTTCTGGAGT[G/T]CCTGGTGAAAAAGCC | 89848 |
| rs372926038 | snp | A/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641338 | GGAGTGGGTTCCAGC[A/T]CTAGAAATGGGAAGG | 89848 |
| rs373029358 | in-del | -/TAAAA | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642522 | AAATAAATAATAAAA[-/TAAAA]CTGCTATAGACATTT | 89848 |
| rs373122765 | snp | C/T | | | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642396 | AGGGTTGAAAAATTA[C/T]CTATCAGGTACAATG | 89848 |
| rs373172811 | snp | G/T | 0.000136554 | 0.00826185 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647459 | TCTGCGGCTTCCAGC[G/T]CAGTGTGGCTCAGGG | 89848 |
| rs373326250 | snp | C/T | 0.000113008 | 0.00751608 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646148 | ATGCTTGGAGCCTCC[C/T]GCTCTGAAGCCTGCT | 89848 |
| rs373523581 | snp | A/T | 3.36276e-05 | 0.00410032 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641666 | GGTTGGAATAACCCC[A/T]CTACATACAATCTCC | 89848 |
| rs373531944 | snp | A/G | 5.39253e-05 | 0.00519228 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647426 | TGCTCCCCGCGGTGG[A/G]CATGCTCCAGGATGA | 89848 |
| rs373548661 | snp | A/G | 0.000103001 | 0.00717564 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649549 | CCCCTCCCCAGAGAA[A/G]GTCTGTGTTGAGGAG | 89848 |
| rs373573627 | snp | C/T | 1.65636e-05 | 0.00287776 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650408 | TTGCTGTAGGATCTG[C/T]GGAGATTGCAGGTCG | 89848 |
| rs373731297 | snp | A/G | 1.64808e-05 | 0.00287057 | stop-lost, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640444 | AGCAGGGAGTATGTG[A/G]GGTGAGTCTGCCTGA | 89848 |
| rs373904180 | snp | A/C/T | 3.35673e-05 | 0.00409668 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644399 | CTCAGCTCCTCTGCA[A/C/T]TCTGTCCGGTGTAGC | 89848 |
| rs373942523 | snp | A/C/G/T | 0.000159599 | 0.00893196 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645077 | CGTGGCCAGGGCTTG[A/C/G/T]GGGGCAGGCTCCTCA | 89848 |
| rs373969125 | snp | C/T | 4.97963e-05 | 0.00498955 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649156 | CCTTGGGCTTCCTCA[C/T]TCTCCATGACCCCAC | 89848 |
| rs374033563 | snp | C/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652854 | TGCCTTCCCCATCCA[C/T]CCATCCAAAGACCAT | 89848 |
| rs374116574 | snp | C/T | 0.000844993 | 0.0205373 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649312 | GTTCTCTGTTCCCTA[C/T]TGGGATGCATACACA | 89848 |
| rs374165937 | snp | C/G | 0.000116637 | 0.00763575 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644728 | AGATATTAGACTTAC[C/G]TCAGCAGTCCATGAC | 89848 |
| rs374170709 | snp | C/G/T | 0.000232124 | 0.0107708 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649461 | ACGGTATCGGTCAGA[C/G/T]GCCTGGAGTCGGGTT | 89848 |
| rs374246765 | in-del | -/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652893 | TCTCCACAATCACTC[-/T]TTTTTTTTTTGAGAT | 89848 |
| rs374341297 | snp | A/G | 1.72439e-05 | 0.00293627 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648046 | GTTAAGCAGGTACTC[A/G]TTGCGGGCTGCTTGC | 89848 |
| rs374563195 | snp | A/G | | | intron-variant, missense | FCHSD1 | GRCh38.p7 | 5:141642491 | GACAAACAAGCACAT[A/G]TACCTCCTGAATCTA | 89848 |
| rs374582822 | snp | C/T | 0.000534143 | 0.0163336 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639476 | CAGTGTGGATGCCAC[C/T]TCCAGCCTGCAGGAC | 89848 |
| rs374637225 | snp | C/T | 0.000196002 | 0.00989759 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649952 | AGCCAGTTTCTGGAG[C/T]GCCTGGTGAAAAAGC | 89848 |
| rs374662473 | snp | C/G | 3.36525e-05 | 0.00410184 | missense, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141639003 | ACAGTGAAGGAGAAG[C/G]GACAGTGCAGCTGTC | 89848 |
| rs374708607 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642192 | GAATGAAATCATGTC[C/T]TCTGCAGCAACATGA | 89848 |
| rs374764272 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649334 | GCATACACAAAGTCC[G/T]TACCTAGACCACCTT | 89848 |
| rs374771802 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649798 | CACGTGCCTTCCCCA[C/T]TTGCTAGGCCTTCAT | 89848 |
| rs374774314 | snp | A/G | 5.52522e-05 | 0.00525576 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647419 | GGTTGTCTGCTCCCC[A/G]CGGTGGGCATGCTCC | 89848 |
| rs374802435 | snp | G/T | | | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646475 | TATTGTGCCACACTG[G/T]TACCTTAAAATACCT | 89848 |
| rs374901920 | snp | A/G | 1.73592e-05 | 0.00294606 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644306 | CCAACACGGCCCCCA[A/G]ATTCTCCCCTCCAGA | 89848 |
| rs374908641 | snp | A/C/G/T | 0.000182165 | 0.00954239 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648933 | CCTCTTCCCTGCCCC[A/C/G/T]ACTCATGCCCTCATC | 89848 |
| rs374920239 | snp | C/T | 1.72564e-05 | 0.00293733 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639631 | GGACAGGGGAGACCA[C/T]TGTGTTCTCTGTGGG | 89848 |
| rs374983485 | snp | A/G | 6.6302e-05 | 0.00575731 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649380 | TCTTCCTTCACCCCA[A/G]CCTCTGAGCCATACC | 89848 |
| rs375045422 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648900 | CCTATGTTCCAAACC[A/G]CTAGACTACTCTGCC | 89848 |
| rs375122300 | snp | A/G | 0.00038463 | 0.0138624 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643018 | CCAGGCAGGACAGGT[A/G]CAGGGGGCCCATCCA | 89848 |
| rs375244135 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646071 | TGGGATCTCTAACCT[C/T]AGGGGTGTGCCTCAC | 89848 |
| rs375369757 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653077 | CAGGGTTTCACCATC[C/T]TTGCCAGGATGGTCT | 89848 |
| rs375499969 | snp | C/T | 4.98087e-05 | 0.00499017 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649148 | TTCCCCAACCTTGGG[C/T]TTCCTCACTCTCCAT | 89848 |
| rs375545779 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643181 | GTTCCTTCCTCATCA[C/T]TTCTCAATACAGGAA | 89848 |
| rs375639972 | snp | C/G | 6.62405e-05 | 0.00575464 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649033 | AGCCTGTGCAGATGA[C/G]AGAAAGGAGTCAGGC | 89848 |
| rs375740679 | snp | A/G | 0.000159987 | 0.00894248 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648975 | GGTGCTCAGTTTCTG[A/G]AGACTGGTCCGAGAG | 89848 |
| rs375785343 | in-del | -/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650509 | GGGAGCGGTTGGGGG[-/G]AGCCAGGTTCCTAGA | 89848 |
| rs375795159 | snp | A/T | 0.00635686 | 0.056018 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640367 | GGGGGCACTGATAGG[A/T]CCTACTCCTGGTCTC | 89848 |
| rs375807322 | snp | A/G | 3.30387e-05 | 0.00406427 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640165 | GCAGCCTAACCCCTC[A/G]TGCACTTGAAGGGAA | 89848 |
| rs375870031 | snp | C/T | 6.69736e-05 | 0.00578639 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644935 | GTCAGCTCATCCTCA[C/T]GCCCTGCCTGGGCCA | 89848 |
| rs375871076 | snp | C/T | 3.30437e-05 | 0.00406457 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638947 | CCCTCTTTTCCTTCT[C/T]CCCTCAGCCAATGCT | 89848 |
| rs376029257 | snp | C/T | 1.74054e-05 | 0.00294998 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646692 | CACTCTTGCCAGCCA[C/T]GCCTTCTGCTCCCCA | 89848 |
| rs376137825 | snp | A/G | 0.000588581 | 0.0171448 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649896 | GCCCACCTGCTGTCC[A/G]TCTCACCGCTCCGGT | 89848 |
| rs376157133 | snp | C/T | 3.4263e-05 | 0.00413888 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645027 | ATTCATACCTGATAG[C/T]GAAATACCACGTGTG | 89848 |
| rs376262095 | snp | A/C/T | 6.65983e-05 | 0.00577021 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639966 | GGACTGCACGAACAC[A/C/T]GTGATGGCTCCCCCA | 89848 |
| rs376302455 | snp | A/G | 4.63177e-05 | 0.00481214 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646154 | GGAGCCTCCCGCTCT[A/G]AAGCCTGCTGCCGCC | 89848 |
| rs376415582 | snp | A/G | 0.000157988 | 0.00888644 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644945 | CCTCACGCCCTGCCT[A/G]GGCCACACACGAAGG | 89848 |
| rs376436093 | snp | C/T | 8.63014e-05 | 0.00656835 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647448 | CCAGGATGACCTCTG[C/T]GGCTTCCAGCTCAGT | 89848 |
| rs376544377 | snp | A/G | 0.000937505 | 0.0216304 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644382 | GTGCCCCCTCAGGGA[A/G]GCTCAGCTCCTCTGC | 89848 |
| rs376640262 | snp | C/T | 0.00019425 | 0.00985329 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642954 | TCCAAGCTTCCTCCT[C/T]CTTCCTGTCTGTTAG | 89848 |
| rs376772696 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645727 | CTTCCACTGGAGTTT[C/T]TCCCTTCTAAGTAAG | 89848 |
| rs376775102 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643867 | AAAAAAAAAAAGAAG[A/G]AGGCTTTACCTCGAT | 89848 |
| rs376789716 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638834 | ACACAGTAGAGAGGA[C/T]TGTTCGCTGCATCAT | 89848 |
| rs377063522 | snp | A/C | 1.68159e-05 | 0.0028996 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644903 | CTATGACCTCCAGCC[A/C]CTCACCCTCCGTGAT | 89848 |
| rs377102108 | snp | C/T | 8.24368e-05 | 0.00641963 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645868 | GCTGGCTTCAGCCAG[C/T]GCTCCACATCTAAGC | 89848 |
| rs377107040 | snp | C/T | 0.000157987 | 0.00888643 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651017 | GGGGGTTGGGGGAGC[C/T]ACCTGATGTCCTCCA | 89848 |
| rs377124228 | snp | A/C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650039 | CAGAGTATAATCATA[A/C/T]CATTCTTTGGGTACA | 89848 |
| rs377153290 | snp | A/C | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652194 | GAACCTCAACTTTTA[A/C]AGCTTTTAAACCTCC | 89848 |
| rs377253130 | snp | G/T | 1.64852e-05 | 0.00287094 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640335 | ACTGGGCTGGGCTCT[G/T]ATTGCTCTCTACTCT | 89848 |
| rs377255467 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645323 | TAATACTAACAGTAA[C/T]AGAGTTACAGTAATT | 89848 |
| rs377288698 | snp | A/G | 3.36865e-05 | 0.00410391 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647494 | CAGGGGGTCCCTCAA[A/G]TGCTCTGACAGCTCA | 89848 |
| rs377400629 | snp | A/C | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651769 | AATTCAGTGTGTGAC[A/C]AGGGAAACTGAGTCA | 89848 |
| rs377441223 | snp | C/G | 0.000163987 | 0.00905353 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647940 | TCCCTCCCTGCTGAG[C/G]GATAGGGGTGTCTGG | 89848 |
| rs377455600 | snp | A/G | 7.6438e-05 | 0.00618168 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643025 | GGACAGGTGCAGGGG[A/G]CCCATCCAACACAGA | 89848 |
| rs377496129 | snp | C/T | 1.68142e-05 | 0.00289945 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641667 | GTTGGAATAACCCCT[C/T]TACATACAATCTCCT | 89848 |
| rs377541658 | snp | G/T | 1.65963e-05 | 0.0028806 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649164 | TTCCTCACTCTCCAT[G/T]ACCCCACCTGGCCTG | 89848 |
| rs377702069 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640458 | GAGGTGAGTCTGCCT[A/G]AGCCCTAAATGAGGT | 89848 |
| rs377708406 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647595 | GCTCGTTCCAGATTT[A/G]ACAGGTGATGGGCAT | 89848 |
| rs397936451 | in-del | -/A | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643862 | CAAAAAAAAAAAAAA[-/A]GAAGAAGGCTTTACC | 89848 |
| rs527522058 | snp | A/G | 3.32984e-05 | 0.00408021 | missense, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141638987 | AAGGAGATGCTGGGG[A/G]ACAGTGAAGGAGAAG | 89848 |
| rs528121221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647289 | TCTCCAACCCTGTCC[C/T]TAGCACTTCTTGGAA | 89848 |
| rs528563407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645667 | AAGCCTCGTAATAAC[C/G]CTTTGAGTTAGGCAC | 89848 |
| rs528798897 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643985 | TGCCCAAGTCATACA[A/G]TAGAAATTTGAACTC | 89848 |
| rs528969637 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643189 | CTCATCACTTCTCAA[A/T]ACAGGAAGTGGCCAA | 89848 |
| rs529037697 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648690 | GTAGTGTTCTCCACT[G/T]TATCCATAATGTCTA | 89848 |
| rs529135233 | snp | C/T | 0.000149285 | 0.00863829 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649191 | CCTGGACATCAGCCG[C/T]CTTCTCCTGTGCCAA | 89848 |
| rs529482734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641870 | ATTAATGGTCACCAT[C/T]CTAGACCATAAAATC | 89848 |
| rs529578464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647722 | CTTTGAGCCCCACTA[G/T]TGCTATAAGATAGGC | 89848 |
| rs529743675 | snp | A/G | | | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642320 | CACATGGACATAGAG[A/G]TGGAAATAACAGACT | 89848 |
| rs529820004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639815 | CCTCCCCTACCTTAG[A/G]CCAGAGGGAAGTAGC | 89848 |
| rs529998555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639201 | AACCATCTCTCTCAT[C/T]TAGATATCATCAAGC | 89848 |
| rs530062926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650505 | AGGAGGGAGCGGTTG[A/G]GGGGAGCCAGGTTCC | 89848 |
| rs530465012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641909 | TATCCACTGTCCTCA[A/G]CATTTATTGGGCAAC | 89848 |
| rs530538036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647340 | GCAAAGAGGGCTGCA[C/T]TGGGAGGGAAGGGTA | 89848 |
| rs530774288 | snp | C/T | 0.000101189 | 0.00711226 | intron-variant, synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641528 | TGGGTGGCCAGGATC[C/T]GGGGCTTTAGCCGGC | 89848 |
| rs530892699 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640857 | AGTCTCTTCTCCTTC[C/T]CCTGCCTGCAACAGG | 89848 |
| rs531059048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646524 | TCCATGACACCCTCA[A/G]TGGCTCCAAGATCCC | 89848 |
| rs531083422 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653076 | ACAGGGTTTCACCAT[A/C]TTTGCCAGGATGGTC | 89848 |
| rs531359287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643229 | TTCGGTGGGGGGGTG[G/T]AGCTGACAAATATTT | 89848 |
| rs531490481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649616 | CCCTGCCCCCTGACC[A/G]ACACCATGGGAGACA | 89848 |
| rs531568957 | in-del | -/CAAGGA | 0.00438332 | 0.0466095 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646809 | CTCTATCTTGACCTC[-/CAAGGA]CAAGGACAAAGAGAA | 89848 |
| rs531905510 | snp | C/T | 0.00039885 | 0.0141162 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639491 | CTCCAGCCTGCAGGA[C/T]GGAGCCCCCTCCCAT | 89848 |
| rs532015620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642379 | GAGTAGAGGCAGGGG[C/T]GAGGGTTGAAAAATT | 89848 |
| rs532038165 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653137 | CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 89848 |
| rs532286514 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640219 | CACTGAGGGCCGGAG[A/G]GAGGGGCCCAAGCCC | 89848 |
| rs532328224 | snp | C/G | 5.43523e-05 | 0.00521279 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644841 | ACCCAAGGTCAGAGC[C/G]CGGGGTCCCATACCC | 89848 |
| rs532487905 | snp | A/G | 1.68527e-05 | 0.00290277 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644418 | GTCCGGTGTAGCTGT[A/G]CAGGGCCTGTGCCAG | 89848 |
| rs532597681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650606 | ACAGGAAACCCTCAC[C/T]TTACTGCCCCGGGCC | 89848 |
| rs532802232 | snp | A/G | 0.000687462 | 0.0185272 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643059 | AGGTGCAGGTGGGGA[A/G]AAGCTGGGAGGAGAA | 89848 |
| rs532927558 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650537 | AGAGTGTAACTACAC[C/G]CAGAGGGAATGGGAC | 89848 |
| rs532987748 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653352 | CCCCAGACCTGGCAC[C/T]AATTAGGTGCACAAT | 89848 |
| rs533326036 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648820 | GAGATCAAGTAAATT[-/A]ACCAAGGTTACCCAC | 89848 |
| rs533515996 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640884 | CAGGCTGCCTGCCCC[A/G]CCTTCCCCAACACCT | 89848 |
| rs533819773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650265 | GACTCTAGGCATCTG[C/T]TCTTGACCACAATAG | 89848 |
| rs534142306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642879 | CCAGAGCCCAGGCAA[A/G]TGCTCTCCACCAAGC | 89848 |
| rs534232693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643309 | CTGCTAGCACTTCAC[A/G]TGTACCAATTCATTC | 89848 |
| rs534549770 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652418 | ACCATCCTAGTCCAA[A/G]CCCCCATTATTAGAC | 89848 |
| rs534561023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640573 | GCTATAAATCCCTTG[G/T]TTTGGTGGTGGAGGT | 89848 |
| rs534654711 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640944 | GAGCAGGCCCCTGCC[C/T]GTGGTGGGCCCCTAA | 89848 |
| rs534670534 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648239 | TAAAAATGTTGCATA[C/T]ACACAACTCCTGCTC | 89848 |
| rs534845479 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642897 | CTCTCCACCAAGCAA[C/G]ATGCCTGAAGGCACG | 89848 |
| rs534935746 | snp | A/G | 0.000399281 | 0.0141238 | splice-acceptor-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639462 | TCCTCCCTGCTGTCC[A/G]GTGTGGATGCCACCT | 89848 |
| rs535010272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644117 | CTGTAGGAGGTAAAA[C/T]TGGGGAGCAGAGGAG | 89848 |
| rs535516043 | snp | A/T | 0.000117935 | 0.00767814 | stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647492 | GTCAGGGGGTCCCTC[A/T]AGTGCTCTGACAGCT | 89848 |
| rs535570933 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650504 | CAGGAGGGAGCGGTT[-/G]GGGGGAGCCAGGTTC | 89848 |
| rs535762962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647897 | ACCCACTGTCATGGG[G/T]ATCAAGAAGCAGGGG | 89848 |
| rs536211348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643820 | ACCATTGCACTCCAG[C/T]CTGGGCAACAAGAGC | 89848 |
| rs536246540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650720 | GCCTTCCAACAGGTC[C/T]GGAAGAGGGAGAGGG | 89848 |
| rs536273607 | snp | A/G | 8.28452e-05 | 0.00643551 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644578 | CCTTTCTTACCTGTG[A/G]GCTCTGCCCCGCAGG | 89848 |
| rs536334100 | snp | C/T | 0.00177054 | 0.0297008 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648935 | TCTTCCCTGCCCCCA[C/T]TCATGCCCTCATCCC | 89848 |
| rs536442553 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649012 | ATCCCATGGTCACTT[C/T]GGTTTAGCCTGTGCA | 89848 |
| rs536764365 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640996 | CTGCCCTCTTAGCAC[A/T]AGAGGCCCAGGCCCT | 89848 |
| rs536772939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643375 | AATAATATGACTCCT[A/G]TGTTAGAAGTGAGAC | 89848 |
| rs537218233 | snp | C/T | 0.000101019 | 0.00710627 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645007 | CATCAGAGGTCCCCA[C/T]CCCCATTCATACCTG | 89848 |
| rs537243609 | snp | A/G | 0.000244254 | 0.0110484 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646214 | GGAAGGCAGAGAACA[A/G]GGGTGGGTGGAAATA | 89848 |
| rs537364155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645199 | ACTCTCAAGCACTGG[G/T]TCTATCTCCCACTCT | 89848 |
| rs537749816 | snp | G/T | 0.00239393 | 0.0345281 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650963 | CACATGTATATTGGG[G/T]AGAAGTGGCGCACAA | 89848 |
| rs537881853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642110 | TCCAGGGAGGGAGAC[C/T]CCTTGTGGACAAGGT | 89848 |
| rs538074045 | in-del | -/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652687 | CTGTCTGCTCACTGT[-/G]CTCCAGCCTCTTTGC | 89848 |
| rs538161141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642842 | AGATGACAGAGCGGG[A/T]CCTGAACCAGTCAGC | 89848 |
| rs538271084 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648823 | ATCAAGTAAATTAAC[C/T]AAGGTTACCCACCCA | 89848 |
| rs538628696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645273 | TGCACCCATCCACTC[A/G]CCATGTACACAACCA | 89848 |
| rs538836274 | snp | A/G | 0.000195408 | 0.0098826 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649909 | CCATCTCACCGCTCC[A/G]GTGCCCTTCCCTCTT | 89848 |
| rs539208005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641216 | TAGAGACCTTGATGG[A/G]TGGTTTCCAGCCCCA | 89848 |
| rs539275680 | snp | A/T | 3.14995e-05 | 0.00396847 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641596 | TTAGTGCTCCAGAGT[A/T]CTCCCTTAAGGGTAT | 89848 |
| rs539878635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643502 | GCTGTATGTATATAC[A/G]TTATAACAACAGATA | 89848 |
| rs540865557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641844 | AGTGGCATTCTATAA[A/G]TATTTGTTAAATTAA | 89848 |
| rs540976615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650863 | GGGGGAGCATTCCTA[A/T]CCAGTATCTGGAGAG | 89848 |
| rs541018848 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642889 | GGCAAGTGCTCTCCA[C/T]CAAGCAAGATGCCTG | 89848 |
| rs541147231 | snp | C/G | 6.63548e-05 | 0.0057596 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640123 | TCCTAGCCAGCCCCC[C/G]AGTACAGAATGGAGG | 89848 |
| rs541222288 | snp | C/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652620 | TGGCCTTCAAGGCTA[C/T]GCATGGAAGACCCTG | 89848 |
| rs541259955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639756 | CTGGACTGGGAGCTC[C/T]GGCAGAAGTCAGGCT | 89848 |
| rs541269326 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643810 | CTGAGATCGCACCAT[C/T]GCACTCCAGCCTGGG | 89848 |
| rs541289455 | snp | C/G | 1.65649e-05 | 0.00287788 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650420 | CTGCGGAGATTGCAG[C/G]TCGGGGGTGAGGTGG | 89848 |
| rs541342592 | snp | A/G | 0.000470865 | 0.0153366 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644338 | GCCGTCATCTACTCC[A/G]TCTTGGGCCCGGGGC | 89848 |
| rs541855186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641329 | GGAAAAAAAGGAGTG[G/T]GTTCCAGCTCTAGAA | 89848 |
| rs541966950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646483 | CACACTGTTACCTTA[A/G]AATACCTTTCCCTCC | 89848 |
| rs542201136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647039 | CTCTCCACGGTGTAC[A/T]CTCACTAAGTTAACA | 89848 |
| rs542672967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649564 | GGTCTGTGTTGAGGA[A/G]GAGAGCACTCCACAG | 89848 |
| rs542920441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647723 | TTTGAGCCCCACTAG[G/T]GCTATAAGATAGGCA | 89848 |
| rs543245703 | snp | C/T | 4.95168e-05 | 0.00497553 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640214 | GCCAACACTGAGGGC[C/T]GGAGGGAGGGGCCCA | 89848 |
| rs543310146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648310 | CCACTGTTCCTTACC[A/G]TGGTCCACCACGTTC | 89848 |
| rs543357830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645508 | GAGATTGCACAGCTC[A/G]TAAGTGGAGTGGCTG | 89848 |
| rs543632419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640614 | CTGGAGCCCCAGGGG[A/G]AAAGCTGGACACAGC | 89848 |
| rs543665295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644751 | TCCATGACCCTGGCT[C/G]TCTTCTACTCAGGCT | 89848 |
| rs544381992 | snp | G/T | 0.00307152 | 0.0390682 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641454 | GTCTGACAGCTTGAA[G/T]ATAGGGACAGCAGCA | 89848 |
| rs544582821 | snp | A/C/G | 4.98785e-05 | 0.00499371 | missense, stop-gained, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641713 | TTACCGGCCTGAGTC[A/C/G]AGGTGCCATCATGTC | 89848 |
| rs544961806 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653087 | CCATCTTTGCCAGGA[G/T]GGTCTCAAACTCCTG | 89848 |
| rs545259031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649075 | GGGAGAATATGAGAT[C/T]AGAGTCAGGCCCAGC | 89848 |
| rs545342313 | snp | A/G | 0.000283889 | 0.0119107 | intron-variant, synonymous-codon | FCHSD1 | GRCh38.p7 | 5:141642447 | TACACTAGAAGCCCA[A/G]TCTCCACCAGTATGC | 89848 |
| rs545790675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645616 | AGGACTCTATGCCAG[A/G]AATTATGCAAAGAAT | 89848 |
| rs545860123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646880 | GTGGACACAGAGATA[A/C]AGAGCTTCAGAAATG | 89848 |
| rs545992845 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651736 | CAGTCCCCGAGCTAA[C/T]GATGAGGAATGGAGA | 89848 |
| rs546259698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641977 | GGGAGATAGGATGCA[C/T]AGTGCTCCCACCCCC | 89848 |
| rs546296136 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642718 | CTGTGTAGTCCACAG[C/G]CATCTTTTTTAACTC | 89848 |
| rs546350255 | snp | A/T | 0 | 0 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648635 | TATTTATTTGCTGTC[A/T]GTCTCTCTTAACCAG | 89848 |
| rs546485558 | snp | C/G/T | 0.00279258 | 0.0372817 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652228 | AACCTGATCCTCCCC[C/G/T]CGTAACGTTTTAAAT | 89848 |
| rs546673178 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644017 | GATCTATCCAGCACT[A/G]AAGTAGGACCCCCCA | 89848 |
| rs546681384 | in-del | -/GT | 0.00279162 | 0.0372561 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648822 | ATCAAGTAAATTAAC[-/GT]CAAGGTTACCCACCC | 89848 |
| rs547285347 | snp | C/G | 1.74814e-05 | 0.00295642 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646684 | CTCCAGGCCACTCTT[C/G]CCAGCCACGCCTTCT | 89848 |
| rs547323573 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640904 | CCCCAACACCTCGCT[C/T]CATATGATAGAGCGT | 89848 |
| rs547457288 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649709 | ACAAGCCTCACTCCT[A/G]CCCTCCACCCCACCC | 89848 |
| rs547915184 | snp | A/T | 4.9722e-05 | 0.00498583 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649401 | GAGCCATACCTTCCT[A/T]AGCACCTGCTCCTTG | 89848 |
| rs548022973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646811 | CTATCTTGACCTCCA[A/G]GGACAAGGACAAAGA | 89848 |
| rs548102860 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651330 | CCGCCAGGAGTCCCC[A/G]TTCAGGGCCAAGCTC | 89848 |
| rs548187714 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640989 | AGGCCCCCTGCCCTC[A/T]TAGCACAAGAGGCCC | 89848 |
| rs548631366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645701 | TGTGATTCCAGTTTT[A/G]TAGGGTTTGCCTTCC | 89848 |
| rs548645262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651206 | GGGCGGGGCCGGGGG[C/G]GTGCTGAGCTCTTTC | 89848 |
| rs548668633 | snp | A/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651762 | GGAGAGGAATTCAGT[A/G]TGTGACCAGGGAAAC | 89848 |
| rs548771740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643191 | CATCACTTCTCAATA[C/T]AGGAAGTGGCCAAAT | 89848 |
| rs548819975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650667 | ATCTGTAGGCTTAGA[C/G]GTGAAGACTGATGGG | 89848 |
| rs548884077 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649207 | CTTCTCCTGTGCCAA[A/G]GCCCACACACGTTCC | 89848 |
| rs549495978 | snp | A/G | | | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640034 | AGGGGGTGGTCAGGG[A/G]TCTGGGGGAGGGCAG | 89848 |
| rs549770478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639227 | CAAGCCTAACATTCA[C/T]CTCTAGTGCCACTCC | 89848 |
| rs549901083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650516 | GTTGGGGGGAGCCAG[A/G]TTCCTAGAGTGTAAC | 89848 |
| rs550054398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639822 | TACCTTAGGCCAGAG[A/G]GAAGTAGCCACCAAA | 89848 |
| rs550299156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647820 | TGCAGCCAGCTAGGA[A/G]CAGAACCAGAGTGCA | 89848 |
| rs550414406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641545 | GGGCTTTAGCCGGCG[C/G]GGGAGGTGGTGGACG | 89848 |
| rs550527850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641927 | TTTATTGGGCAACTG[C/G]TGTATAATCAGCTCT | 89848 |
| rs550549331 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649759 | AGCTCCTCTGCTGCT[G/T]CTGTGTCAGCTCTAC | 89848 |
| rs551016096 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640880 | GCAACAGGCTGCCTG[C/T]CCCGCCTTCCCCAAC | 89848 |
| rs551246668 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652029 | CTTCCAGCCCTAGCA[C/T]TGCTTCCTGAGGAGC | 89848 |
| rs551599510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643725 | TGGCAGCACGTGCCT[A/G]TAATCCCAGCTACTC | 89848 |
| rs551678974 | in-del | -/AG | 0.000118364 | 0.00769208 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647480 | TGGCTCAGGGAGGTC[-/AG]GGGGTCCCTCAAGTG | 89848 |
| rs551710082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643230 | TCGGTGGGGGGGTGT[A/G]GCTGACAAATATTTC | 89848 |
| rs551783972 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648901 | CTATGTTCCAAACCA[C/G]TAGACTACTCTGCCT | 89848 |
| rs552274097 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650708 | CGATGTCTGCCAGCC[C/T]TCCAACAGGTCTGGA | 89848 |
| rs552339218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650613 | ACCCTCACCTTACTG[C/T]CCCGGGCCCCAGCAG | 89848 |
| rs552613580 | snp | C/G | 0.000731755 | 0.0191139 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651122 | GCCGGCTTCACCTGT[C/G]GGGGCAAAGAGAGGA | 89848 |
| rs552652553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639399 | GCATGCTGAAAGAAC[A/G]TAAGAAACAAAACAT | 89848 |
| rs552734693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641633 | CTATTCCCTCAGCCC[C/T]GCAGACAAAACAGGA | 89848 |
| rs552805996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646978 | GAGGTGTGTTTTTTT[A/G]TGTGTGTCCTGTTGG | 89848 |
| rs552894518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641239 | CAGCCCCAGAGATTT[C/G]AGGCATTTCACCACC | 89848 |
| rs553134419 | snp | A/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652497 | ACCCACTGTTCACAC[A/G]GCACTCAGAGTGATC | 89848 |
| rs553398650 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640527 | TTTCGGCTCCCTGAA[-/C]CCCCCCGAGTAAACT | 89848 |
| rs553449967 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650911 | GGCTGTGGATGGGTC[A/G]GCTGGGGAGCTCTTG | 89848 |
| rs553504266 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650280 | CTCTTGACCACAATA[C/G]GGATAGGTATGGACA | 89848 |
| rs554260952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642288 | CTCACTTATAAGTGG[A/G]AGCTAAACAACGGGT | 89848 |
| rs554348821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642911 | AGATGCCTGAAGGCA[A/C]GGAGAGGACCAGAGC | 89848 |
| rs554481833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645415 | TTCATAATGACCCAG[G/T]GTTAATAGTTTTGCA | 89848 |
| rs554594458 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651481 | CTGCCCGCCCACGAC[C/T]TGTCCGGCGACGTCG | 89848 |
| rs554655827 | snp | A/C | 4.97566e-05 | 0.00498757 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640124 | CCTAGCCAGCCCCCC[A/C]GTACAGAATGGAGGA | 89848 |
| rs554721773 | snp | G/T | 3.332e-05 | 0.00408153 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639481 | TGGATGCCACCTCCA[G/T]CCTGCAGGACGGAGC | 89848 |
| rs554765287 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652621 | GGCCTTCAAGGCTAC[C/G]CATGGAAGACCCTGC | 89848 |
| rs554792651 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642963 | CCTCCTTCTTCCTGT[A/C]TGTTAGCCTCCCAAG | 89848 |
| rs555325168 | snp | C/G | 0.00208891 | 0.0322505 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647910 | GGGATCAAGAAGCAG[C/G]GGGAGGTCCTCCTTT | 89848 |
| rs555413085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642049 | AATAAATGACTAAGT[A/G]CTAAGTCATGCAAAG | 89848 |
| rs555587172 | snp | A/C | 3.35801e-05 | 0.00409743 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641674 | TAACCCCTCTACATA[A/C]AATCTCCTCCAAGGC | 89848 |
| rs555605182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647052 | ACACTCACTAAGTTA[A/T]CACAAAACAAAGATA | 89848 |
| rs555747255 | snp | A/G | 1.68267e-05 | 0.00290053 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647504 | CTCAAGTGCTCTGAC[A/G]GCTCACTGACCAGGG | 89848 |
| rs555866509 | in-del | -/C | 0.0103295 | 0.0711199 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651439 | CACTATGGAGCCCCG[-/C]CCCCAGGCCAGGTCA | 89848 |
| rs556343041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650728 | ACAGGTCTGGAAGAG[A/G]GAGAGGGATTCTGCC | 89848 |
| rs556350876 | snp | A/C/G | 8.2945e-05 | 0.00643948 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649472 | CAGACGCCTGGAGTC[A/C/G]GGTTTGGCCCCCAGC | 89848 |
| rs556405536 | in-del | -/AGTC | 0.00528939 | 0.0511539 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645124 | CCTCACATTCCTCAA[-/AGTC]AGAAAGCTCAGCATC | 89848 |
| rs556582702 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643368 | CATTTTTAATAATAT[G/T]ACTCCTATGTTAGAA | 89848 |
| rs556725126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646855 | GCCTACAGTCATGGA[C/T]ACAGGTAATGTGGAC | 89848 |
| rs556863623 | snp | C/G/T | 0.000117973 | 0.00767937 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640626 | GGGAAAAGCTGGACA[C/G/T]AGCTTGAACAGGAAG | 89848 |
| rs556933991 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640725 | CAGGGGGTGGGTGGG[C/T]GTGAAAGCCCTCCCC | 89848 |
| rs556991972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641077 | TTACAGCTGCTTCGC[A/C]TCCTGGCTCCAGCTC | 89848 |
| rs557584724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645203 | TCAAGCACTGGTTCT[A/G]TCTCCCACTCTTCCA | 89848 |
| rs558059738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642845 | TGACAGAGCGGGACC[G/T]GAACCAGTCAGCCTG | 89848 |
| rs558331342 | snp | A/G | 0.000347397 | 0.0131749 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648039 | CCACCAAGTTAAGCA[A/G]GTACTCATTGCGGGC | 89848 |
| rs558581166 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651429 | GAAGCCCCGCCCACT[A/G]TGGAGCCCCGCCCCA | 89848 |
| rs558644593 | snp | C/T | 9.93789e-05 | 0.00704837 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644650 | GGGAAGTTGAGATAT[C/T]GCTCAGGGACAAAGC | 89848 |
| rs558709366 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644000 | ATAGAAATTTGAACT[A/C]AGATCTATCCAGCAC | 89848 |
| rs558868440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650159 | TATTCCCATTTCACA[A/G]AGAAAGAAACTGAGG | 89848 |
| rs559176808 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640719 | CAGGGCCAGGGGGTG[A/G]GTGGGCGTGAAAGCC | 89848 |
| rs559338094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646461 | ACTGTGCTCTTAACT[A/G]TTGTGCCACACTGTT | 89848 |
| rs559449441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645630 | GAAATTATGCAAAGA[A/G]TGATATATGATGATT | 89848 |
| rs559791229 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651746 | GCTAATGATGAGGAA[C/T]GGAGAGGAATTCAGT | 89848 |
| rs559845471 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643161 | TTCCTCTCATCCCAT[C/G]TCCAGTTCCTTCCTC | 89848 |
| rs560685318 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642090 | TGGTGGAGATGGTGG[-/T]TAACTCCAGGGAGGG | 89848 |
| rs560686372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641855 | ATAAATATTTGTTAA[A/G]TTAATGGTCACCATC | 89848 |
| rs560798832 | snp | A/G | 0.000259051 | 0.011378 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641509 | GCCTTCAGGTGAGGG[A/G]ATCTGGGTGGCCAGG | 89848 |
| rs561128514 | snp | A/C/T | 0.000463745 | 0.0152206 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650422 | GCGGAGATTGCAGGT[A/C/T]GGGGGTGAGGTGGGG | 89848 |
| rs561193305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639160 | TATAGGAAGAAAGTT[A/G]TTTTGTAGAAATCGC | 89848 |
| rs561261833 | snp | C/T | 0.000199501 | 0.00998553 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644718 | CAATGTGAACAGATA[C/T]TAGACTTACCTCAGC | 89848 |
| rs561748645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647789 | CGGAAGAGTTTAAGT[G/T]TACTGTACAATGCCA | 89848 |
| rs562236997 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640839 | GAGAGGTCACAGCCC[C/T]TCAGTCTCTTCTCCT | 89848 |
| rs562404525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643708 | AGAAAATTAGCCGGG[C/T]GTGGCAGCACGTGCC | 89848 |
| rs562534167 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646011 | CCCTTCCTTCCTCCC[-/A]CCATCAGAAAGAGGA | 89848 |
| rs562727099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643226 | GCATTCGGTGGGGGG[A/G]TGTAGCTGACAAATA | 89848 |
| rs563157402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641904 | CACTCTATCCACTGT[C/T]CTCAACATTTATTGG | 89848 |
| rs563233016 | snp | C/T | | | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639390 | TTTTAAGGAGCATGC[C/T]GAAAGAACGTAAGAA | 89848 |
| rs563364475 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651603 | GCGGACGCAGCGTCC[A/G]CTGGGCGGTGGGAAG | 89848 |
| rs563399305 | snp | C/T | 1.66338e-05 | 0.00288386 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639896 | AGTTGTGGTCCTAAA[C/T]CCCAGTGTTCCCTCC | 89848 |
| rs563476939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650979 | AGAAGTGGCGCACAA[A/C]GACGAAGGTGAGTGT | 89848 |
| rs563760600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642547 | ATAGACATTTAAAAA[A/G]GAAAAAAAGTGGGCA | 89848 |
| rs563760739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649110 | GTGACTTGGCTCCAC[C/G]CCTAGACAGCCCCAC | 89848 |
| rs564451342 | snp | G/T | | | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641716 | CCGGCCTGAGTCGAG[G/T]TGCCATCATGTCCAG | 89848 |
| rs564470861 | in-del | -/T | 0.00263466 | 0.0361993 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643111 | GGGGTGGGCACAGAG[-/T]TTATTCCTGGCATGT | 89848 |
| rs564562335 | snp | C/T | 0.000109033 | 0.00738274 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641456 | CTGACAGCTTGAAGA[C/T]AGGGACAGCAGCATC | 89848 |
| rs565170093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649673 | GGGAGCCCATCAATC[A/G]ATCAGCCCATTAGCT | 89848 |
| rs565216720 | snp | C/T | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650396 | GCTGCCCTCTGCTTG[C/T]TGTAGGATCTGCGGA | 89848 |
| rs565535059 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650097 | CTTATAGTCATTAAT[C/T]TGTTTAATCCTTACA | 89848 |
| rs565537229 | snp | A/G | 1.65641e-05 | 0.00287781 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644635 | GGGAGGGAGAGGTCC[A/G]GGAAGTTGAGATATC | 89848 |
| rs565679679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640538 | CTGAACCCCCCGAGT[A/T]AACTGCAGGCTTAGC | 89848 |
| rs566221202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650206 | AACTTGTCCAAGGTC[A/G]CATGGCTATAATTAC | 89848 |
| rs566230003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650617 | TCACCTTACTGCCCC[C/G]GGCCCCAGCAGGATC | 89848 |
| rs566331392 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641989 | GCATAGTGCTCCCAC[C/G]CCCAATGGCTGTCAA | 89848 |
| rs566735507 | snp | G/T | 0.000304589 | 0.012337 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647477 | GTGTGGCTCAGGGAG[G/T]TCAGGGGGTCCCTCA | 89848 |
| rs567162640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650684 | TGAAGACTGATGGGG[A/G]CCTGGGTACGATGTC | 89848 |
| rs567614101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649722 | CTGCCCTCCACCCCA[A/C]CCACAGTGTCCTTGC | 89848 |
| rs567630037 | snp | A/G/T | 0.00149129 | 0.0272661 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649462 | CGGTATCGGTCAGAC[A/G/T]CCTGGAGTCGGGTTT | 89848 |
| rs568147191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646812 | TATCTTGACCTCCAA[C/G]GACAAGGACAAAGAG | 89848 |
| rs568319196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647584 | CTGTAAAATAGGCTC[A/G]TTCCAGATTTGACAG | 89848 |
| rs568704952 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650951 | CCTCCACCCCAGCAC[A/G]TGTATATTGGGGAGA | 89848 |
| rs568734907 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651230 | CTCTTTCCTCTGTTA[C/G]TTCTGGTTTGGGGTC | 89848 |
| rs569089746 | in-del | -/GGCGGGGCG | 0.00119737 | 0.0244387 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651573 | CGGCAGGGTCCGGGT[-/GGCGGGGCG]GGCGGGGCGGACGCA | 89848 |
| rs569093458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642839 | TGGAGATGACAGAGC[A/G]GGACCTGAACCAGTC | 89848 |
| rs569131951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642058 | CTAAGTGCTAAGTCA[C/T]GCAAAGTGAACTTGG | 89848 |
| rs569638806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651287 | ACCACAAGTCGGATG[C/T]CCCCTTAGCTCCCTC | 89848 |
| rs569676381 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652173 | CTCTGCTAGTATATC[C/T]AATAGGAACCTCAAC | 89848 |
| rs569678362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645213 | GTTCTATCTCCCACT[C/T]TTCCATCTTTCCTCT | 89848 |
| rs569885781 | snp | C/G | 4.97888e-05 | 0.00498918 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649483 | AGTCGGGTTTGGCCC[C/G]CAGCCACGGTGGCAT | 89848 |
| rs569924469 | snp | A/G | 0.000295873 | 0.0121593 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649881 | CTCCCCCTCCATAGG[A/G]CCCACCTGCTGTCCA | 89848 |
| rs569973650 | snp | C/T | 0.00013207 | 0.00812512 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640191 | GGGAACCCCAGAGCT[C/T]CTGCAGAGCCAACAC | 89848 |
| rs570051558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639308 | TATGGTCACTAACAT[C/G]TTAATATTGAGTTTA | 89848 |
| rs570245868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641968 | CAAAACTAAGGGAGA[C/T]AGGATGCATAGTGCT | 89848 |
| rs570597398 | snp | C/T | 5.41863e-05 | 0.00520483 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648120 | GTAAACTGATGTCAA[C/T]AGGAAGCCCTAGACC | 89848 |
| rs570976701 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640883 | ACAGGCTGCCTGCCC[C/T]GCCTTCCCCAACACC | 89848 |
| rs571156836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640529 | TTCGGCTCCCTGAAC[C/T]CCCCGAGTAAACTGC | 89848 |
| rs571672110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642846 | GACAGAGCGGGACCT[G/T]AACCAGTCAGCCTGG | 89848 |
| rs572034845 | snp | A/C | 0.000251174 | 0.0112038 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640087 | TGGAGAGGCTGCCCC[A/C]TGAGAGGCCACAGCC | 89848 |
| rs572116378 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651477 | CCCTCTGCCCGCCCA[A/C]GACTTGTCCGGCGAC | 89848 |
| rs572286753 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640517 | CTATTTAAGCCTTTC[A/G]GCTCCCTGAACCCCC | 89848 |
| rs572311087 | snp | A/G | 0.000132503 | 0.00813842 | stop-gained, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644651 | GGAAGTTGAGATATC[A/G]CTCAGGGACAAAGCC | 89848 |
| rs572666915 | snp | C/T | 0.000117888 | 0.00767659 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641662 | GACTGGTTGGAATAA[C/T]CCCTCTACATACAAT | 89848 |
| rs572777481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641251 | TTTCAGGCATTTCAC[C/T]ACCCTAGATAGGGTC | 89848 |
| rs572899583 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648694 | TGTTCTCCACTGTAT[C/T]CATAATGTCTAGAAC | 89848 |
| rs572960461 | snp | A/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652545 | TTAAAGGGAAATAAG[A/G]TCTCATAATTTACTT | 89848 |
| rs573268180 | in-del | -/A | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640869 | TCCCCTGCCTGCAAC[-/A]AGGCTGCCTGCCCCG | 89848 |
| rs573274887 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652892 | ATCACTCTTTTTTTT[A/T]TGAGATGGAGTCTTG | 89848 |
| rs573531628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643572 | GGCTTTGCCTCGGCG[C/G]GGCGCAGTGGCTCAT | 89848 |
| rs573553545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650284 | TGACCACAATAGGGA[A/T]AGGTATGGACAGACA | 89848 |
| rs574076932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642926 | CGGAGAGGACCAGAG[C/T]GTGACCTGGGAGTCC | 89848 |
| rs574168742 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640713 | AGCTGGCAGGGCCAG[C/G]GGGTGGGTGGGCGTG | 89848 |
| rs574188306 | snp | A/C/G | 0.000132478 | 0.00813782 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648986 | TCTGGAGACTGGTCC[A/C/G]AGAGTGGAAGATCCC | 89848 |
| rs574295123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642290 | CACTTATAAGTGGGA[A/G]CTAAACAACGGGTAC | 89848 |
| rs574548893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645431 | GTTAATAGTTTTGCA[C/T]AACTATTAACCTCAC | 89848 |
| rs574587182 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640136 | CCCAGTACAGAATGG[A/C]GGACTCAGGGACAGC | 89848 |
| rs574938463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648368 | TGACCTCTTTTCAAG[C/T]GCTTGTTCCCTTGCT | 89848 |
| rs575557501 | snp | A/C | 6.7113e-05 | 0.00579241 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641675 | AACCCCTCTACATAC[A/C]ATCTCCTCCAAGGCA | 89848 |
| rs575676935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647055 | CTCACTAAGTTAACA[C/G]AAAACAAAGATAATG | 89848 |
| rs575872002 | snp | C/G | 3.31367e-05 | 0.00407029 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651081 | GGATGCTCAGCTGTT[C/G]CAGGAAGCGAAGCTT | 89848 |
| rs576376834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643420 | CTGTCCAAAATCACG[A/G]AGCCAGTTATTGGCA | 89848 |
| rs576585440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643418 | AGCTGTCCAAAATCA[C/T]GAAGCCAGTTATTGG | 89848 |
| rs576705731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646384 | GTCACTCCCTTACCT[A/G]GGGCTACAGAACTAG | 89848 |
| rs576779647 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651612 | GCGTCCGCTGGGCGG[C/T]GGGAAGAACCCCAGG | 89848 |
| rs576869840 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652784 | TCTCCTCCTTCCAGC[A/G]TTCCATCTGTCGCCT | 89848 |
| rs576935504 | snp | G/T | 0.000119296 | 0.0077223 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640631 | AAGCTGGACACAGCT[G/T]GAACAGGAAGCAACA | 89848 |
| rs577317069 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648518 | GCAAGGCCAGCTCCT[C/T]CTTGACAGTTAGGCC | 89848 |
| rs578047979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642249 | TGAACTAACTCAGAA[A/G]CAGAAAACCAAATAT | 89848 |
| rs745334394 | snp | A/G | 0.000148428 | 0.00861347 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640471 | CTGAGCCCTAAATGA[A/G]GTAATCTCATCTTCC | 89848 |
| rs745344233 | snp | C/G | 1.74336e-05 | 0.00295237 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648036 | TAGCCACCAAGTTAA[C/G]CAGGTACTCATTGCG | 89848 |
| rs745412488 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638829 | TGAGGACACAGTAGA[A/G]AGGATTGTTCGCTGC | 89848 |
| rs745429918 | snp | A/G | 2.96222e-05 | 0.0038484 | stop-gained, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645845 | CCTCATCCTGGGCCT[A/G]GGTCATGGCTGGCTT | 89848 |
| rs745521691 | snp | G/T | 6.31852e-05 | 0.00562037 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646044 | AGAGGGAGTGGGGCT[G/T]GCCTGAGAAGGTGGG | 89848 |
| rs745630631 | snp | C/T | 7.07426e-05 | 0.00594696 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646655 | GCTCGGCTGGTCAAG[C/T]GCTGAACCTCTTTCT | 89848 |
| rs745727010 | snp | A/G | 9.73283e-05 | 0.00697529 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649933 | CCCTCTTCAGGAATG[A/G]GCCAGCCAGTTTCTG | 89848 |
| rs745843745 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650378 | CCATACTCCCGTTCA[A/G]TGGCTGCCCTCTGCT | 89848 |
| rs745898536 | snp | C/T | 1.67237e-05 | 0.00289164 | stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649512 | ATCCAGCAGGCAGCG[C/T]CAGGCACCGAACACT | 89848 |
| rs745936031 | snp | C/T | 1.80237e-05 | 0.00300192 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645110 | GAGCTCTCCCGTCTC[C/T]TCACATTCCTCAAAG | 89848 |
| rs746006757 | snp | A/G | | | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648976 | GTGCTCAGTTTCTGG[A/G]GACTGGTCCGAGAGT | 89848 |
| rs746013868 | snp | C/T | 1.65902e-05 | 0.00288008 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639499 | TGCAGGACGGAGCCC[C/T]CTCCCATCATCACAC | 89848 |
| rs746027577 | snp | C/T | 1.66211e-05 | 0.00288275 | synonymous-codon, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641729 | AGGTGCCATCATGTC[C/T]AGGAACCCAGGGAAG | 89848 |
| rs746090848 | in-del | -/CCCCAG | 1.68536e-05 | 0.00290285 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647556 | CTGACACCACCCTTC[-/CCCCAG]ACCTCTACTGTAAAA | 89848 |
| rs746101960 | snp | C/T | 8.42169e-05 | 0.00648856 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639609 | AAGGAAGGAAAAAGC[C/T]GCCCCCGGACAGGGG | 89848 |
| rs746202061 | snp | C/G | 2.07682e-05 | 0.00322237 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647365 | AGGGTAAAAAGGATC[C/G]CCGGGGAAGCTCTTA | 89848 |
| rs746224402 | snp | A/T | 3.33333e-05 | 0.00408235 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649504 | ACGGTGGCATCCAGC[A/T]GGCAGCGCCAGGCAC | 89848 |
| rs746301997 | snp | A/G | 0.000100708 | 0.00709535 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644914 | AGCCACTCACCCTCC[A/G]TGATTGTCAGCTCAT | 89848 |
| rs746392666 | snp | A/G | 6.96282e-05 | 0.00589994 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645049 | CCACGTGTGCAGGGC[A/G]GGGGAGGGCCCTCGT | 89848 |
| rs746485048 | snp | C/G | 2.69139e-05 | 0.00366827 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646074 | GATCTCTAACCTCAG[C/G]GGTGTGCCTCACCTG | 89848 |
| rs746485998 | snp | C/T | 3.30666e-05 | 0.00406598 | synonymous-codon, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141638956 | CCTTCTTCCCTCAGC[C/T]AATGCTGAGGCCTTG | 89848 |
| rs746738334 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648634 | GTATTTATTTGCTGT[C/T]TGTCTCTCTTAACCA | 89848 |
| rs746779052 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650392 | AATGGCTGCCCTCTG[C/T]TTGCTGTAGGATCTG | 89848 |
| rs746786469 | snp | A/T | 1.64773e-05 | 0.00287026 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640392 | GGTCTCTCATTGTTG[A/T]CCCCTCCCCTTTCTC | 89848 |
| rs746866729 | snp | C/T | 1.7235e-05 | 0.00293551 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648047 | TTAAGCAGGTACTCA[C/T]TGCGGGCTGCTTGCA | 89848 |
| rs746892693 | snp | A/G | 8.59513e-05 | 0.00655502 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650983 | GTGGCGCACAACGAC[A/G]AAGGTGAGTGTAAAT | 89848 |
| rs746969998 | in-del | -/CCC | 0.000186643 | 0.00965849 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647364 | AAGGGTAAAAAGGAT[-/CCC]CGGGGAAGCTCTTAG | 89848 |
| rs746986817 | snp | C/T | 1.65663e-05 | 0.002878 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648910 | AAACCACTAGACTAC[C/T]CTGCCTCCCTCTTCC | 89848 |
| rs747016028 | snp | C/T | 5.07335e-05 | 0.00503629 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639615 | GGAAAAAGCCGCCCC[C/T]GGACAGGGGAGACCA | 89848 |
| rs747021247 | in-del | -/C | 1.66651e-05 | 0.00288657 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644545 | CTCCATACCCAGGGT[-/C]CTCTAACCCAAAATT | 89848 |
| rs747037804 | snp | A/G | 7.68197e-05 | 0.00619709 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643034 | CAGGGGGCCCATCCA[A/G]CACAGAGGTAGGTGC | 89848 |
| rs747077790 | snp | G/T | 1.65737e-05 | 0.00287864 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649283 | TGCAGCACCTCAGCC[G/T]GCGCCCTCTGGAGGT | 89848 |
| rs747193124 | in-del | -/T | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141651699 | AATTATTGATAATTA[-/T]TCATTTGCATATGTA | 89848 |
| rs747211053 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650562 | TGGGACTGATGGGAG[C/T]CCTTGAGATCACCTC | 89848 |
| rs747261920 | snp | A/G | 0.00011396 | 0.00754765 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647092 | GCCTAAATCATAATC[A/G]CCTTTATATGTGGCC | 89848 |
| rs747364930 | snp | C/G | 3.37052e-05 | 0.00410505 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647878 | AGACAAGATCCCCTG[C/G]ACCACCCACTGTCAT | 89848 |
| rs747429830 | snp | A/C | 1.82914e-05 | 0.00302413 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645160 | CAGCCTAGAGGGGCA[A/C]AGAACAGACCTCATA | 89848 |
| rs747485602 | snp | C/T | 6.62789e-05 | 0.00575631 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644675 | CAAAGCCTACCTCGC[C/T]GTGCTGGTTCCGAGC | 89848 |
| rs747566287 | snp | A/G | 1.65795e-05 | 0.00287914 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649208 | TTCTCCTGTGCCAAG[A/G]CCCACACACGTTCCC | 89848 |
| rs747658757 | snp | C/T | 3.35402e-05 | 0.00409499 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644919 | CTCACCCTCCGTGAT[C/T]GTCAGCTCATCCTCA | 89848 |
| rs747660127 | in-del | -/T | | | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640286 | CAAACCAGACACTTC[-/T]GATCACCAGGTAGGA | 89848 |
| rs747731609 | snp | A/G | 1.65323e-05 | 0.00287505 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640146 | AATGGAGGACTCAGG[A/G]ACAGCAGCCTAACCC | 89848 |
| rs747856921 | snp | A/G | 9.86631e-05 | 0.00702295 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649876 | TGGCCCTCCCCCTCC[A/G]TAGGGCCCACCTGCT | 89848 |
| rs747931152 | snp | A/C | 8.01186e-05 | 0.00632873 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651158 | ACCCCAGCGCAAGGA[A/C]CTAAAAAACACTCCG | 89848 |
| rs747933170 | snp | A/C | 1.65614e-05 | 0.00287757 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648932 | CCCTCTTCCCTGCCC[A/C]CACTCATGCCCTCAT | 89848 |
| rs747974596 | snp | C/T | 2.41514e-05 | 0.00347493 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646088 | GGGGTGTGCCTCACC[C/T]GTGCCCGGCGGATGC | 89848 |
| rs748019454 | snp | A/C/G | 4.96819e-05 | 0.00498386 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649013 | TCCCATGGTCACTTC[A/C/G]GTTTAGCCTGTGCAG | 89848 |
| rs748083136 | in-del | -/G | 7.18894e-05 | 0.00599496 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639652 | TCTCTGTGGGCAGGT[-/G]GGGCAGGTGCTCCAG | 89848 |
| rs748099162 | snp | C/T | 1.67033e-05 | 0.00288987 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639475 | CCAGTGTGGATGCCA[C/T]CTCCAGCCTGCAGGA | 89848 |
| rs748110860 | in-del | -/GTG | 1.85132e-05 | 0.00304241 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643125 | AGTTATTCCTGGCAT[-/GTG]GGGAGGTTTTACCAG | 89848 |
| rs748145584 | snp | A/G | 2.19305e-05 | 0.00331131 | missense, stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646139 | CTCTGTTCTATGCTT[A/G]GAGCCTCCCGCTCTG | 89848 |
| rs748182762 | snp | G/T | 1.68829e-05 | 0.00290537 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640021 | GGGGACAGGACCCAG[G/T]GGGTGGTCAGGGGTC | 89848 |
| rs748193836 | snp | C/T | | | intron-variant, missense | FCHSD1 | GRCh38.p7 | 5:141642494 | AAACAAGCACATGTA[C/T]CTCCTGAATCTAAAA | 89848 |
| rs748206004 | snp | A/C | 4.75613e-05 | 0.00487631 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647117 | GTGGCCTGGTTCCAA[A/C]AAGCAGGAAGATCTC | 89848 |
| rs748292285 | snp | C/T | 1.87926e-05 | 0.00306528 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644817 | GAGAAGTCCCTCCTA[C/T]TGCCCCCAACCCAAG | 89848 |
| rs748298402 | snp | A/G | 2.9734e-05 | 0.00385566 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647237 | CCAGCTTACCTAGGG[A/G]TTGGGAAAAGTCAAA | 89848 |
| rs748390098 | snp | C/T | 6.74855e-05 | 0.00580846 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644895 | TCCCTCCTCTATGAC[C/T]TCCAGCCACTCACCC | 89848 |
| rs748411110 | snp | C/T | 7.55886e-05 | 0.00614724 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640653 | GAAGCAACAGTGTTA[C/T]TCTTCCTCTTCTCCA | 89848 |
| rs748417592 | snp | A/G | 3.3243e-05 | 0.00407681 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651009 | TAAATGAAGGGGGTT[A/G]GGGGAGCTACCTGAT | 89848 |
| rs748485413 | snp | C/G | 0.000173596 | 0.00931493 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642535 | AATAAAACTGCTATA[C/G]ACATTTAAAAAAGAA | 89848 |
| rs748525660 | snp | C/G | 2.54036e-05 | 0.00356387 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645822 | ACTGAGCCGCCGCTC[C/G]TGCTCCACCTCATCC | 89848 |
| rs748622836 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649352 | CCTAGACCACCTTTG[A/G]TCCCAAGCCAGCTCT | 89848 |
| rs748760265 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646936 | GAATGAAAAGGATGG[C/T]GCAGTCAAGTGACTG | 89848 |
| rs748761599 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642996 | TCCCAGTTCCTTCCA[C/G]TCACCCCCAGGCAGG | 89848 |
| rs748779251 | snp | G/T | 3.29788e-05 | 0.00406058 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640259 | CACTCAAGAGGCAAA[G/T]GGGCAGCCAAGCAAA | 89848 |
| rs748781500 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642923 | GCACGGAGAGGACCA[C/G]AGCGTGACCTGGGAG | 89848 |
| rs748788130 | snp | G/T | 1.64849e-05 | 0.00287092 | intron-variant, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640341 | CTGGGCTCTTATTGC[G/T]CTCTACTCTGGGGGG | 89848 |
| rs748848996 | snp | C/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644530 | CCCCTAACAATTTTT[C/G]TCCATACCCAGGGTC | 89848 |
| rs748917090 | in-del | -/GGA | 9.03302e-05 | 0.00671989 | cds-indel, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643066 | GGTGGGGAGAAGCTG[-/GGA]GGAGAAGGGGACGGC | 89848 |
| rs748921476 | snp | C/T | | | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646092 | TGTGCCTCACCTGTG[C/T]CCGGCGGATGCTCTC | 89848 |
| rs748927477 | snp | A/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645166 | AGAGGGGCAAAGAAC[A/T]GACCTCATATGGGGC | 89848 |
| rs749002061 | snp | C/G | 3.55942e-05 | 0.00421851 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648024 | GGTGGGCATTGGTAG[C/G]CACCAAGTTAAGCAG | 89848 |
| rs749046772 | in-del | -/G | 1.65674e-05 | 0.00287809 | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639534 | CACCTGGGCTCTGCA[-/G]CCCCTTGCCTCCATT | 89848 |
| rs749053271 | snp | C/T | 1.65982e-05 | 0.00288077 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649158 | TTGGGCTTCCTCACT[C/T]TCCATGACCCCACCT | 89848 |
| rs749263807 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650510 | GGAGCGGTTGGGGGG[A/C]GCCAGGTTCCTAGAG | 89848 |
| rs749289577 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644883 | TTCGTCAGCATCTCC[C/G]TCCTCTATGACCTCC | 89848 |
| rs749294578 | in-del | -/AGTT | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648525 | CAGCTCCTTCTTGAC[-/AGTT]AGGCCACCTATTCAG | 89848 |
| rs749309379 | snp | C/T | 3.36163e-05 | 0.00409963 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644906 | TGACCTCCAGCCACT[C/T]ACCCTCCGTGATTGT | 89848 |
| rs749443948 | snp | G/T | 4.53114e-05 | 0.00475959 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641530 | GGTGGCCAGGATCCG[G/T]GGCTTTAGCCGGCGG | 89848 |
| rs749453990 | snp | C/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647689 | AGAAGTTTAAAACAC[C/G]TTCACATCCATTCTC | 89848 |
| rs749461250 | snp | C/G | 0.000110552 | 0.00743397 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651318 | CGTTCCCCCAGCCCG[C/G]CAGGAGTCCCCATTC | 89848 |
| rs749536250 | snp | C/G | 1.65611e-05 | 0.00287755 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649023 | ACTTCGGTTTAGCCT[C/G]TGCAGATGAGAGAAA | 89848 |
| rs749538736 | snp | C/T | 3.37399e-05 | 0.00410717 | missense, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141639006 | GTGAAGGAGAAGGGA[C/T]AGTGCAGCTGTCCAG | 89848 |
| rs749653270 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648676 | CAGGAACTCCATTGG[C/T]AGTGTTCTCCACTGT | 89848 |
| rs749701664 | snp | A/G | 1.68633e-05 | 0.00290368 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640026 | CAGGACCCAGGGGGT[A/G]GTCAGGGGTCTGGGG | 89848 |
| rs749738737 | snp | C/G | 1.65776e-05 | 0.00287898 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649453 | GCTAGGTCACGGTAT[C/G]GGTCAGACGCCTGGA | 89848 |
| rs749739903 | snp | A/G | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652365 | CAACAATAAACAAAC[A/G]AAAACCTCTTGATCC | 89848 |
| rs749748663 | snp | C/T | 0.000121282 | 0.00778629 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647147 | CACCTGATCAGTCCC[C/T]GCTGGCTGAAACTGC | 89848 |
| rs749774266 | snp | A/C | 5.00304e-05 | 0.00500127 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640103 | TGAGAGGCCACAGCC[A/C]CAGGTCCTAGCCAGC | 89848 |
| rs749794987 | snp | A/C | 3.42331e-05 | 0.00413707 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647259 | AAAGTCAAAGTCACT[A/C]ATTCACTGACTCACT | 89848 |
| rs749873764 | snp | A/T | 1.65666e-05 | 0.00287802 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650439 | GGGGTGAGGTGGGGG[A/T]TAAGGTTATGTTTGG | 89848 |
| rs749885164 | snp | C/T | 1.71185e-05 | 0.00292557 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644870 | CCACCTTGACCCATT[C/T]GTCAGCATCTCCCTC | 89848 |
| rs749894770 | in-del | -/CTT | 9.72337e-05 | 0.0069719 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141642952 | AGTCCAAGCTTCCTC[-/CTT]CTTCCTGTCTGTTAG | 89848 |
| rs749977277 | snp | C/T | 7.6234e-05 | 0.00617343 | intron-variant, synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641499 | GGCTTCCCTGGCCTT[C/T]AGGTGAGGGGATCTG | 89848 |
| rs750011500 | snp | A/G | 9.01591e-05 | 0.00671353 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651085 | GCTCAGCTGTTCCAG[A/G]AAGCGAAGCTTCACC | 89848 |
| rs750065628 | snp | A/G | 0.000264595 | 0.011499 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641560 | GGGGAGGTGGTGGAC[A/G]CATCTGTAGGGAACA | 89848 |
| rs750077240 | snp | C/T | 1.65168e-05 | 0.00287369 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638942 | TGACTCCCTCTTTTC[C/T]TTCTTCCCTCAGCCA | 89848 |
| rs750189566 | snp | C/G | 0.00011853 | 0.00769747 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644197 | GGTGCCTGGGGAGTT[C/G]AGGGAGAAGGTAAGC | 89848 |
| rs750207148 | snp | A/G | 1.65899e-05 | 0.00288005 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639925 | CCCCTCCCAGGTTCC[A/G]GGTGACACACATTGA | 89848 |
| rs750208431 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644757 | ACCCTGGCTCTCTTC[C/T]ACTCAGGCTTCTAGC | 89848 |
| rs750285326 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643160 | TTTCCTCTCATCCCA[C/T]CTCCAGTTCCTTCCT | 89848 |
| rs750287792 | snp | G/T | 1.98482e-05 | 0.00315019 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646762 | AGGAGGACCTGAGGC[G/T]GCTCCTTCTCTCCAG | 89848 |
| rs750295136 | snp | A/G | 1.68057e-05 | 0.00289872 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640003 | GGAGCTGGGGCTCTG[A/G]TGGGGGACAGGACCC | 89848 |
| rs750324934 | snp | G/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642051 | TAAATGACTAAGTGC[G/T]AAGTCATGCAAAGTG | 89848 |
| rs750331202 | snp | C/T | 5.09918e-05 | 0.00504909 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647185 | GGGTGGGGGAAAATA[C/T]ACCAGGCTCCTGAAG | 89848 |
| rs750364398 | snp | G/T | 3.32829e-05 | 0.00407925 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644724 | GAACAGATATTAGAC[G/T]TACCTCAGCAGTCCA | 89848 |
| rs750534773 | snp | A/C | 4.69164e-05 | 0.00484314 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645799 | TCCCTCTGGGACAGC[A/C]GAGCCTCACTGAGCC | 89848 |
| rs750549626 | snp | G/T | | | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646429 | GAATTTGAACCTATG[G/T]CGGTCTAGCTCCAAA | 89848 |
| rs750639872 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645602 | ATAAAAATGTACTGA[A/G]GACTCTATGCCAGAA | 89848 |
| rs750653383 | snp | C/T | 6.8764e-05 | 0.00586321 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645907 | TGCAGCAGGGCCAGC[C/T]GGGCAGCCCCCTTCA | 89848 |
| rs750797330 | snp | A/G | 1.65061e-05 | 0.00287277 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640210 | CAGAGCCAACACTGA[A/G]GGCCGGAGGGAGGGG | 89848 |
| rs750942078 | snp | C/T | | | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649914 | TCACCGCTCCGGTGC[C/T]CTTCCCTCTTCAGGA | 89848 |
| rs750956141 | snp | A/G | 4.96915e-05 | 0.0049843 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650332 | GAGGCTGGAACAAGA[A/G]GTAAGGTCCAGAGAA | 89848 |
| rs750958132 | snp | C/T | 0.000136472 | 0.00825939 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647856 | GTATCATCTACTCAC[C/T]CTAAACAGACAAGAT | 89848 |
| rs750997803 | snp | C/G | 0.000139709 | 0.00835672 | intron-variant, downstream-variant-500B | FCHSD1, RELL2 | GRCh38.p7 | 5:141641576 | CATCTGTAGGGAACA[C/G]ACAGTTAGTGCTCCA | 89848 |
| rs750999645 | snp | A/C | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648989 | GGAGACTGGTCCGAG[A/C]GTGGAAGATCCCATG | 89848 |
| rs751036347 | snp | C/G | 0.000366412 | 0.0135304 | utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651400 | CGGTCAGCCACTGGA[C/G]TCCGGAACTGGAGGA | 89848 |
| rs751122042 | snp | G/T | 1.69499e-05 | 0.00291112 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639450 | CCCTCACTCCCCTCC[G/T]CCCTGCTGTCCAGTG | 89848 |
| rs751126510 | snp | C/T | 3.332e-05 | 0.00408153 | splice-donor-variant | FCHSD1 | GRCh38.p7 | 5:141641701 | AGGCAAGGGCCCTTA[C/T]CGGCCTGAGTCGAGG | 89848 |
| rs751138777 | snp | C/T | 0.000166058 | 0.00911051 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649125 | CCCTAGACAGCCCCA[C/T]CTCCCTGTTCCCCAA | 89848 |
| rs751203921 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650151 | ATTATTATTATTCCC[A/G]TTTCACAGAGAAAGA | 89848 |
| rs751205892 | snp | C/T | 4.98956e-05 | 0.00499453 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639579 | AGGCCTCCACTTGTC[C/T]GTCAGGGACGCTCCA | 89848 |
| rs751435282 | snp | A/G | 1.6904e-05 | 0.00290719 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644890 | GCATCTCCCTCCTCT[A/G]TGACCTCCAGCCACT | 89848 |
| rs751438420 | snp | A/G | | | intron-variant, utr-variant-3-prime | FCHSD1 | GRCh38.p7 | 5:141642380 | AGTAGAGGCAGGGGC[A/G]AGGGTTGAAAAATTA | 89848 |
| rs751462091 | snp | G/T | 3.33879e-05 | 0.00408568 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644970 | CGAAGGATTCAGGAC[G/T]TGGCTGTCCCCCACC | 89848 |
| rs751472467 | snp | C/G | 5.72721e-05 | 0.00535096 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651124 | CGGCTTCACCTGTGG[C/G]GGCAAAGAGAGGATG | 89848 |
| rs751496067 | in-del | -/A | 0.00295955 | 0.0383538 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651161 | CCAGCGCAAGGACCT[-/A]AAAAACACTCCGCGC | 89848 |
| rs751531449 | snp | A/G | 1.66599e-05 | 0.00288611 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641515 | AGGTGAGGGGATCTG[A/G]GTGGCCAGGATCCGG | 89848 |
| rs751682681 | snp | A/C | 3.10844e-05 | 0.00394224 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644212 | CAGGGAGAAGGTAAG[A/C]CTCACCTGTTCAGGG | 89848 |
| rs751736435 | snp | C/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647069 | ACAAAACAAAGATAA[C/T]GGAGGAGGCCTAAAT | 89848 |
| rs751770059 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649346 | TCCTTACCTAGACCA[C/T]CTTTGGTCCCAAGCC | 89848 |
| rs751861439 | snp | A/G | 8.28562e-05 | 0.00643593 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649424 | GCTCCTTGGCGCTCC[A/G]CCCTGTACCCCCTGC | 89848 |
| rs751925327 | snp | G/T | 1.88354e-05 | 0.00306877 | stop-gained, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647998 | CAGTTCCTCCTGGTA[G/T]TAATGGTCGAGGTGG | 89848 |
| rs751928779 | snp | C/T | 0.000115393 | 0.00759493 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640337 | TGGGCTGGGCTCTTA[C/T]TGCTCTCTACTCTGG | 89848 |
| rs752063289 | snp | A/G | 2.47081e-05 | 0.00351475 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645815 | GAGCCTCACTGAGCC[A/G]CCGCTCCTGCTCCAC | 89848 |
| rs752123507 | snp | G/T | 0.000123115 | 0.00784489 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646285 | TTGCATCACATACAT[G/T]ATGTCATTTAATCTT | 89848 |
| rs752134327 | snp | G/T | 1.64787e-05 | 0.00287038 | synonymous-codon, utr-variant-3-prime, missense | RELL2, FCHSD1 | GRCh38.p7 | 5:141640435 | ACCACAGGGAGCAGG[G/T]AGTATGTGAGGTGAG | 89848 |
| rs752183725 | snp | A/G | 3.3151e-05 | 0.00407117 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649242 | GCCCATACAGCTTCC[A/G]ACTTCGGCTCAGCTC | 89848 |
| rs752273514 | snp | A/C | 3.32989e-05 | 0.00408024 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639881 | GCCAAGCAGCCTCTG[A/C]GTTGTGGTCCTAAAC | 89848 |
| rs752322270 | snp | A/G | 3.5529e-05 | 0.00421465 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646635 | GGATCTTGTAGTCAC[A/G]GGCAGCTCGGCTGGT | 89848 |
| rs752327260 | in-del | -/TTAA | | | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646454 | CCAAAAACTGTGCTC[-/TTAA]TTAACTATTGTGCCA | 89848 |
| rs752330892 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640575 | TATAAATCCCTTGGT[C/T]TGGTGGTGGAGGTAG | 89848 |
| rs752353646 | snp | C/G | 0.000218814 | 0.0104575 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651075 | TCTGAAGGATGCTCA[C/G]CTGTTCCAGGAAGCG | 89848 |
| rs752372868 | in-del | -/AG | 1.83667e-05 | 0.00303034 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646734 | ACACCTGAATGGGTC[-/AG]GGGGTGCTGTGAGGA | 89848 |
| rs752377848 | in-del | -/CTGCCCT | 1.6561e-05 | 0.00287753 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650382 | ACTCCCGTTCAATGG[-/CTGCCCT]CTGCTTGCTGTAGGA | 89848 |
| rs752410472 | snp | C/G | 1.65649e-05 | 0.00287788 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644616 | ACTGTCTTGGCTGCT[C/G]TCTGGGAGGGAGAGG | 89848 |
| rs752443423 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650225 | GGCTATAATTACACA[A/G]CAGGGATCTGACACC | 89848 |
| rs752493279 | snp | A/T | 1.67161e-05 | 0.00289098 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644983 | ACTTGGCTGTCCCCC[A/T]CCCTTGCCCATCAGA | 89848 |
| rs752561214 | snp | C/T | 1.66399e-05 | 0.00288438 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641707 | GGGCCCTTACCGGCC[C/T]GAGTCGAGGTGCCAT | 89848 |
| rs752573902 | snp | C/G | 3.14579e-05 | 0.00396585 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641597 | TAGTGCTCCAGAGTT[C/G]TCCCTTAAGGGTATC | 89848 |
| rs752602206 | snp | A/G | 0.000166237 | 0.00911542 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646314 | TTCCCTATGAGGTGG[A/G]TGCTATTATTGGCCC | 89848 |
| rs752606136 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645450 | TATTAACCTCACTTT[A/G]TTTACAAGGAAACTG | 89848 |
| rs752660227 | snp | A/C | 1.65996e-05 | 0.00288089 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649154 | AACCTTGGGCTTCCT[A/C]ACTCTCCATGACCCC | 89848 |
| rs752792352 | snp | A/G | 9.94266e-05 | 0.00705007 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649438 | CGCCCTGTACCCCCT[A/G]CTAGGTCACGGTATC | 89848 |
| rs752821611 | snp | C/G | 0.00246974 | 0.0350538 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640083 | GCCATGGAGAGGCTG[C/G]CCCCTGAGAGGCCAC | 89848 |
| rs752911612 | snp | C/T | 1.65176e-05 | 0.00287376 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640170 | CTAACCCCTCGTGCA[C/T]TTGAAGGGAACCCCA | 89848 |
| rs752915840 | snp | C/T | | | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638878 | GGGTCTAGCATAGCC[C/T]CTTGCTCCCTCTTCT | 89848 |
| rs752937207 | snp | C/T | 1.68145e-05 | 0.00289948 | intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641481 | AGCATCACTGGGGGT[C/T]AAGGCTTCCCTGGCC | 89848 |
| rs752975574 | snp | A/G | 1.8234e-05 | 0.00301938 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647421 | TTGTCTGCTCCCCGC[A/G]GTGGGCATGCTCCAG | 89848 |
| rs753024861 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638934 | ACCTCCACTGACTCC[C/T]TCTTTTCCTTCTTCC | 89848 |
| rs753037580 | snp | C/T | 3.29457e-05 | 0.00405854 | synonymous-codon, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638802 | TCCTTCAGCTGAGGA[C/T]GATGACATGAATGAG | 89848 |
| rs753074024 | snp | A/G | 1.7119e-05 | 0.00292562 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141645960 | GGAAGTAAGTTAGTG[A/G]AACCTGGCTGACGGC | 89848 |
| rs753104438 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648567 | CCCTCTAAATTCTAC[A/C]CCCTTGTTATTCTTT | 89848 |
| rs753183915 | snp | C/T | 1.65605e-05 | 0.0028775 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648952 | CATGCCCTCATCCCT[C/T]GAACCTTGGTGCTCA | 89848 |
| rs753246462 | snp | A/G | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646736 | ACCTGAATGGGTCAG[A/G]GGGTGCTGTGAGGAG | 89848 |
| rs753297657 | snp | A/G | 1.88756e-05 | 0.00307204 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646746 | GTCAGGGGGTGCTGT[A/G]AGGAGGACCTGAGGC | 89848 |
| rs753343728 | in-del | -/C | 0.000198863 | 0.00996956 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649432 | GCGCTCCGCCCTGTA[-/C]CCCCTGCTAGGTCAC | 89848 |
| rs753386411 | snp | A/G | 1.6604e-05 | 0.00288127 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644707 | TGCTCACCCAGCAAT[A/G]TGAACAGATATTAGA | 89848 |
| rs753476247 | snp | A/G | 1.80091e-05 | 0.0030007 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644843 | CCAAGGTCAGAGCCC[A/G]GGGTCCCATACCCAC | 89848 |
| rs753483882 | snp | C/T | 3.31214e-05 | 0.00406935 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650372 | ACCTGCCCATACTCC[C/T]GTTCAATGGCTGCCC | 89848 |
| rs753495707 | in-del | -/CAGCGCTCCA | 7.77741e-05 | 0.00623546 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645865 | ATGGCTGGCTTCAGC[-/CAGCGCTCCA]CATCTAAGCCAGCCC | 89848 |
| rs753577979 | snp | A/G | 6.62625e-05 | 0.00575559 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650432 | CAGGTCGGGGGTGAG[A/G]TGGGGGATAAGGTTA | 89848 |
| rs753619183 | snp | C/G | 2.12881e-05 | 0.00326246 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645763 | GTAGTGTTGGGGGAG[C/G]AGCTCACGGTTGGAG | 89848 |
| rs753619371 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141652999 | TCTGCTTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 89848 |
| rs753624568 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640776 | CCCAGCTGAGGGACC[A/C]GCTCTACTTCCACCT | 89848 |
| rs753715266 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651436 | CGCCCACTATGGAGC[C/T]CCGCCCCAGGCCAGG | 89848 |
| rs753728564 | snp | A/G | 1.65759e-05 | 0.00287883 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649249 | CAGCTTCCGACTTCG[A/G]CTCAGCTCCCGGACA | 89848 |
| rs753780210 | snp | C/T | 1.7796e-05 | 0.0029829 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646643 | TAGTCACGGGCAGCT[C/T]GGCTGGTCAAGCGCT | 89848 |
| rs753814408 | snp | A/T | 1.66142e-05 | 0.00288216 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639904 | TCCTAAACCCCAGTG[A/T]TCCCTCCCCTCCCAG | 89848 |
| rs753894866 | snp | A/T | 1.74805e-05 | 0.00295634 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649571 | GTTGAGGAGGAGAGC[A/T]CTCCACAGCTTCATG | 89848 |
| rs753907980 | snp | C/T | | | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639107 | CTCCCAGCCTCCTTG[C/T]ATGTATGGGGTTGGG | 89848 |
| rs753934444 | snp | C/G | 1.68741e-05 | 0.00290461 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647566 | CCTTCCCCCAGACCT[C/G]TACTGTAAAATAGGC | 89848 |
| rs754021283 | snp | C/T | 1.79345e-05 | 0.00299448 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645103 | CCTCAAAGAGCTCTC[C/T]CGTCTCCTCACATTC | 89848 |
| rs754088739 | snp | A/G | 2.17815e-05 | 0.00330004 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141639067 | AGCTTGCCTTGGAGA[A/G]TATCCTCTCCTCCAG | 89848 |
| rs754207950 | snp | C/T | 2.14231e-05 | 0.00327278 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646108 | CCGGCGGATGCTCTC[C/T]CGCACTTCCTGTAAC | 89848 |
| rs754230231 | snp | A/G | 0.000397384 | 0.0140902 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649057 | GTCAGGCCCACCCCA[A/G]GTGGGAGAATATGAG | 89848 |
| rs754320124 | snp | A/G | 0.000329609 | 0.0128334 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646195 | TCGTTGCAGTACCTG[A/G]TTGGGAAGGCAGAGA | 89848 |
| rs754382567 | snp | A/G | 1.72829e-05 | 0.00293959 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644468 | GAGAGACGGTGAGAG[A/G]GAGGTGGGTAGCAGT | 89848 |
| rs754458941 | snp | G/T | 1.6607e-05 | 0.00288153 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649143 | CCCTGTTCCCCAACC[G/T]TGGGCTTCCTCACTC | 89848 |
| rs754542725 | snp | A/G | 8.94094e-05 | 0.00668556 | intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646252 | GCATGACTTACTATG[A/G]GACTGGTACTTTGCT | 89848 |
| rs754650904 | in-del | -/AG | 2.79513e-05 | 0.0037383 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646072 | GGGATCTCTAACCTC[-/AG]GGGTGTGCCTCACCT | 89848 |
| rs754668990 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650165 | CATTTCACAGAGAAA[G/T]AAACTGAGGTCAAGA | 89848 |
| rs754712147 | snp | C/T | 5.07009e-05 | 0.00503467 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644891 | CATCTCCCTCCTCTA[C/T]GACCTCCAGCCACTC | 89848 |
| rs754723278 | snp | A/C | 1.74366e-05 | 0.00295263 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644486 | GGTGGGTAGCAGTGC[A/C]CCAGGACCATGACAC | 89848 |
| rs754750729 | snp | C/G | 3.31505e-05 | 0.00407113 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649433 | CGCTCCGCCCTGTAC[C/G]CCCTGCTAGGTCACG | 89848 |
| rs754778592 | in-del | -/AG | 0.000139441 | 0.00834871 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141643108 | AGGTGGGGTGGGCAC[-/AG]AGTTATTCCTGGCAT | 89848 |
| rs754808520 | snp | A/C | 4.99563e-05 | 0.00499756 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641520 | AGGGGATCTGGGTGG[A/C]CAGGATCCGGGGCTT | 89848 |
| rs754881036 | snp | C/T | 0.000116968 | 0.00764658 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644978 | TCAGGACTTGGCTGT[C/T]CCCCACCCTTGCCCA | 89848 |
| rs754885388 | snp | A/G | 1.67492e-05 | 0.00289384 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141651130 | CACCTGTGGGGGCAA[A/G]GAGAGGATGAAGACC | 89848 |
| rs754933675 | snp | C/G | 6.61704e-05 | 0.00575159 | missense, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141638963 | CCCTCAGCCAATGCT[C/G]AGGCCTTGAAGGAGA | 89848 |
| rs754961732 | snp | C/G | 3.38897e-05 | 0.00411627 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141641584 | GGGAACACACAGTTA[C/G]TGCTCCAGAGTTCTC | 89848 |
| rs755006468 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141648990 | GAGACTGGTCCGAGA[A/G]TGGAAGATCCCATGG | 89848 |
| rs755092091 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653234 | CAGCACTAAACTCAC[A/T]TGTTCAAGTACTGGT | 89848 |
| rs755112405 | snp | C/G | 1.65778e-05 | 0.002879 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649347 | CCTTACCTAGACCAC[C/G]TTTGGTCCCAAGCCA | 89848 |
| rs755198422 | snp | A/G | 0.000102659 | 0.00716372 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647110 | TTTATATGTGGCCTG[A/G]TTCCAACAAGCAGGA | 89848 |
| rs755332630 | snp | C/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645748 | TCTAAGTAAGGATGG[C/G]TAGTGTTGGGGGAGG | 89848 |
| rs755337622 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640440 | AGGGAGCAGGGAGTA[C/T]GTGAGGTGAGTCTGC | 89848 |
| rs755401987 | snp | A/G | 8.79144e-05 | 0.00662944 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648103 | GGCGGACAGCTAGGA[A/G]GGTAAACTGATGTCA | 89848 |
| rs755434454 | snp | C/T | 2.48599e-05 | 0.00352552 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645817 | GCCTCACTGAGCCGC[C/T]GCTCCTGCTCCACCT | 89848 |
| rs755523768 | snp | A/G | 1.66746e-05 | 0.00288739 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643048 | AACACAGAGGTAGGT[A/G]CAGGTGGGGAGAAGC | 89848 |
| rs755530150 | snp | C/T | 3.38295e-05 | 0.00411262 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645924 | GGCAGCCCCCTTCAC[C/T]TGGCTCACCTGCCAT | 89848 |
| rs755576019 | snp | A/C | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647093 | CCTAAATCATAATCG[A/C]CTTTATATGTGGCCT | 89848 |
| rs755611664 | snp | A/G | 1.77178e-05 | 0.00297634 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646637 | ATCTTGTAGTCACGG[A/G]CAGCTCGGCTGGTCA | 89848 |
| rs755640892 | snp | C/G | 1.67343e-05 | 0.00289255 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644532 | CCTAACAATTTTTCT[C/G]CATACCCAGGGTCCT | 89848 |
| rs755690784 | in-del | -/C | 8.28329e-05 | 0.00643503 | splice-donor-variant, intron-variant | FCHSD1 | GRCh38.p7 | 5:141642999 | AGTTCCTTCCACTCA[-/C]CCCCCAGGCAGGACA | 89848 |
| rs755713229 | in-del | -/A | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646875 | GTAATGTGGACACAG[-/A]GATACAGAGCTTCAG | 89848 |
| rs755741628 | snp | C/G/T | 3.29708e-05 | 0.00406011 | intron-variant, utr-variant-3-prime, missense, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640340 | GCTGGGCTCTTATTG[C/G/T]TCTCTACTCTGGGGG | 89848 |
| rs755843926 | snp | C/G | | | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639724 | TGATCCCAAAAGTGG[C/G]CCTTGGCTCTTTCCT | 89848 |
| rs755862357 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650363 | AAGTCCCATACCTGC[C/T]CATACTCCCGTTCAA | 89848 |
| rs755880965 | snp | A/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644758 | CCCTGGCTCTCTTCT[A/T]CTCAGGCTTCTAGCT | 89848 |
| rs755893549 | in-del | -/T | 1.6591e-05 | 0.00288015 | frameshift-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639501 | CAGGACGGAGCCCCC[-/T]CCCATCATCACACAG | 89848 |
| rs755970520 | snp | G/T | | | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650250 | GACACCAGTCTGCTT[G/T]ACTCTAGGCATCTGC | 89848 |
| rs755971201 | snp | C/G | 1.77865e-05 | 0.0029821 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645084 | AGGGCTTGGGGGGCA[C/G]GCTCCTCAAAGAGCT | 89848 |
| rs755998573 | snp | A/G | 1.66015e-05 | 0.00288105 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649155 | ACCTTGGGCTTCCTC[A/G]CTCTCCATGACCCCA | 89848 |
| rs756057008 | snp | C/T | 0.000116406 | 0.00762819 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641712 | CTTACCGGCCTGAGT[C/T]GAGGTGCCATCATGT | 89848 |
| rs756107881 | snp | C/T | 1.66632e-05 | 0.0028864 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639590 | TGTCCGTCAGGGACG[C/T]TCCAAGGAAGGAAAA | 89848 |
| rs756165394 | snp | A/G | 3.0276e-05 | 0.00389064 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647242 | TTACCTAGGGGTTGG[A/G]AAAAGTCAAAGTCAC | 89848 |
| rs756404236 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653416 | GTCTTTTGGTTCCCA[C/G]GTTTATTGACAATTA | 89848 |
| rs756471597 | snp | C/G/T | 3.30214e-05 | 0.00406323 | intron-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141638936 | CTCCACTGACTCCCT[C/G/T]TTTTCCTTCTTCCCT | 89848 |
| rs756511233 | snp | A/G | 2.23381e-05 | 0.00334194 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646098 | TCACCTGTGCCCGGC[A/G]GATGCTCTCTCGCAC | 89848 |
| rs756579831 | snp | C/T | 6.44849e-05 | 0.00567788 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644247 | AGAGTTCAGGTGGCC[C/T]TGGGGGGCCAAGCAG | 89848 |
| rs756602837 | snp | C/G | 1.67427e-05 | 0.00289328 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644362 | CCGGGGCAGCAGACG[C/G]ATGAGTGCCCCCTCA | 89848 |
| rs756634349 | snp | A/G | 3.37513e-05 | 0.00410786 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640022 | GGGACAGGACCCAGG[A/G]GGTGGTCAGGGGTCT | 89848 |
| rs756649281 | snp | C/G | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649443 | TGTACCCCCTGCTAG[C/G]TCACGGTATCGGTCA | 89848 |
| rs756756396 | snp | A/G | 1.66101e-05 | 0.0028818 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141644709 | CTCACCCAGCAATGT[A/G]AACAGATATTAGACT | 89848 |
| rs756834829 | snp | C/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141650373 | CCTGCCCATACTCCC[C/G]TTCAATGGCTGCCCT | 89848 |
| rs756888862 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, intron-variant | RELL2, HDAC3, FCHSD1 | GRCh38.p7 | 5:141638811 | TGAGGACGATGACAT[C/G]AATGAGGACACAGTA | 89848 |
| rs756924791 | snp | A/G | 1.65655e-05 | 0.00287793 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650435 | GTCGGGGGTGAGGTG[A/G]GGGATAAGGTTATGT | 89848 |
| rs756945719 | snp | C/T | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141641940 | TGCTGTATAATCAGC[C/T]CTGCTCAAGGTACAA | 89848 |
| rs757019688 | snp | A/C | 1.65759e-05 | 0.00287883 | stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649257 | GACTTCGGCTCAGCT[A/C]CCGGACAGACTGCAG | 89848 |
| rs757107001 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640862 | CTTCTCCTTCCCCTG[C/T]CTGCAACAGGCTGCC | 89848 |
| rs757109602 | in-del | -/GAG | 0.000189975 | 0.00974429 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649559 | GAGAAGGTCTGTGTT[-/GAG]GAGGAGAGCACTCCA | 89848 |
| rs757112558 | snp | C/T | 7.92864e-05 | 0.00629579 | synonymous-codon, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643008 | CCACTCACCCCCAGG[C/T]AGGACAGGTGCAGGG | 89848 |
| rs757114672 | snp | A/C | 1.67728e-05 | 0.00289588 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639605 | CTCCAAGGAAGGAAA[A/C]AGCCGCCCCCGGACA | 89848 |
| rs757146825 | snp | A/G | 7.11605e-05 | 0.00596449 | stop-gained, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646644 | AGTCACGGGCAGCTC[A/G]GCTGGTCAAGCGCTG | 89848 |
| rs757180578 | snp | G/T | 1.65762e-05 | 0.00287886 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649315 | CTCTGTTCCCTATTG[G/T]GATGCATACACAAAG | 89848 |
| rs757202616 | snp | C/T | 1.65982e-05 | 0.00288077 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639913 | CCAGTGTTCCCTCCC[C/T]TCCCAGGTTCCGGGT | 89848 |
| rs757236404 | snp | C/G | 3.8219e-05 | 0.00437127 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646751 | GGGGTGCTGTGAGGA[C/G]GACCTGAGGCTGCTC | 89848 |
| rs757236574 | snp | G/T | 1.65633e-05 | 0.00287774 | missense, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644640 | GGAGAGGTCCGGGAA[G/T]TTGAGATATCGCTCA | 89848 |
| rs757271005 | snp | C/T | 5.17665e-05 | 0.0050873 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645037 | GATAGCGAAATACCA[C/T]GTGTGCAGGGCAGGG | 89848 |
| rs757340034 | snp | C/T | | | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639322 | TCTTAATATTGAGTT[C/T]ATTAGATAAAGACAA | 89848 |
| rs757602874 | snp | G/T | 1.66233e-05 | 0.00288295 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641717 | CGGCCTGAGTCGAGG[G/T]GCCATCATGTCCAGG | 89848 |
| rs757716395 | snp | A/G | 1.66721e-05 | 0.00288717 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640105 | AGAGGCCACAGCCCC[A/G]GGTCCTAGCCAGCCC | 89848 |
| rs757770703 | snp | C/G | 5.22871e-05 | 0.00511281 | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141644475 | GGTGAGAGGGAGGTG[C/G]GTAGCAGTGCCCCAG | 89848 |
| rs757804785 | snp | A/C | 9.08538e-05 | 0.00673933 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649583 | AGCACTCCACAGCTT[A/C]ATGAGACCACCCCCA | 89848 |
| rs757848582 | snp | A/C | 5.4447e-05 | 0.00521733 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651117 | CCTGGGCCGGCTTCA[A/C]CTGTGGGGGCAAAGA | 89848 |
| rs757901068 | snp | C/G | 0.000271813 | 0.0116547 | intron-variant, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RELL2, FCHSD1 | GRCh38.p7 | 5:141641506 | CTGGCCTTCAGGTGA[C/G]GGGATCTGGGTGGCC | 89848 |
| rs757997759 | snp | C/T | 1.84582e-05 | 0.00303789 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141648135 | TAGGAAGCCCTAGAC[C/T]CCCAGAGTCCTTCCA | 89848 |
| rs758082791 | snp | A/G | 1.73423e-05 | 0.00294463 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639429 | TGAAGGGAAATGGAA[A/G]TGTTACCCTCACTCC | 89848 |
| rs758085479 | snp | A/G | 3.02403e-05 | 0.00388834 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141646058 | TTGCCTGAGAAGGTG[A/G]GATCTCTAACCTCAG | 89848 |
| rs758102055 | snp | G/T | 1.68103e-05 | 0.00289911 | synonymous-codon, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640004 | GAGCTGGGGCTCTGG[G/T]GGGGGACAGGACCCA | 89848 |
| rs758139303 | snp | A/G | 3.335e-05 | 0.00408337 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647088 | GGAGGCCTAAATCAT[A/G]ATCGCCTTTATATGT | 89848 |
| rs758139897 | in-del | -/G | 4.37206e-05 | 0.0046753 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141651074 | TCTGAAGGATGCTCA[-/G]GCTGTTCCAGGAAGC | 89848 |
| rs758193236 | in-del | -/G | 2.59145e-05 | 0.00359952 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647174 | CTGCTGAGGTGGGGT[-/G]GGGGAAAATACACCA | 89848 |
| rs758230313 | snp | A/C | | | upstream-variant-2KB | FCHSD1 | GRCh38.p7 | 5:141652316 | CTACCCCTACATTCT[A/C]TCCATCAGTAAGTCC | 89848 |
| rs758315339 | snp | C/T | 2.57483e-05 | 0.00358796 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647196 | AATACACCAGGCTCC[C/T]GAAGAAACAGCTTCA | 89848 |
| rs758379983 | snp | C/G | 1.64969e-05 | 0.00287196 | intron-variant, utr-variant-3-prime, downstream-variant-500B | RELL2, FCHSD1 | GRCh38.p7 | 5:141640482 | ATGAGGTAATCTCAT[C/G]TTCCCATCACCTACT | 89848 |
| rs758397042 | snp | A/T | 3.32967e-05 | 0.0040801 | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141641748 | AACCCAGGGAAGTCC[A/T]GGGCTTTGTCTGGAA | 89848 |
| rs758432246 | snp | A/G | 1.65677e-05 | 0.00287812 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141650441 | GGTGAGGTGGGGGAT[A/G]AGGTTATGTTTGGTC | 89848 |
| rs758451941 | snp | A/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141642155 | GTTTTAGAAAAGGCA[A/G]GCATTCCACAGCCAT | 89848 |
| rs758576192 | snp | C/T | 1.66646e-05 | 0.00288652 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141643030 | GGTGCAGGGGGCCCA[C/T]CCAACACAGAGGTAG | 89848 |
| rs758660917 | snp | C/G | | | intron-variant, downstream-variant-500B | FCHSD1 | GRCh38.p7 | 5:141645613 | CTGAGGACTCTATGC[C/G]AGAAATTATGCAAAG | 89848 |
| rs758669271 | snp | A/G | 1.65745e-05 | 0.00287871 | synonymous-codon, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649261 | TCGGCTCAGCTCCCG[A/G]ACAGACTGCAGCACC | 89848 |
| rs758736680 | snp | C/T | | | missense, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644611 | TTGTCACTGTCTTGG[C/T]TGCTCTCTGGGAGGG | 89848 |
| rs758748925 | snp | A/G | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644589 | TGTGGGCTCTGCCCC[A/G]CAGGGATTGTCACTG | 89848 |
| rs758790646 | snp | C/G | 5.97604e-05 | 0.00546595 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141649841 | CTGGGGCTGAGCTCC[C/G]CATCACTTTTTGGCC | 89848 |
| rs758826992 | snp | A/G | 3.31301e-05 | 0.00406989 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141644598 | TGCCCCGCAGGGATT[A/G]TCACTGTCTTGGCTG | 89848 |
| rs758833121 | snp | A/G | 1.65048e-05 | 0.00287265 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640212 | GAGCCAACACTGAGG[A/G]CCGGAGGGAGGGGCC | 89848 |
| rs758853023 | snp | A/G | 1.7339e-05 | 0.00294435 | intron-variant | FCHSD1 | GRCh38.p7 | 5:141647859 | TCATCTACTCACTCT[A/G]AACAGACAAGATCCC | 89848 |
| rs758921383 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant, utr-variant-3-prime, synonymous-codon | RELL2, FCHSD1 | GRCh38.p7 | 5:141640328 | GGACTGCACTGGGCT[A/G]GGCTCTTATTGCTCT | 89848 |
| rs758942806 | snp | C/T | 1.80883e-05 | 0.00300729 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141645121 | TCTCCTCACATTCCT[C/T]AAAGTCAGAAAGCTC | 89848 |
| rs758944691 | snp | A/G | 4.0563e-05 | 0.00450332 | missense, intron-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141647975 | AAACTGGCCTTGAGC[A/G]GAGCTGGCAGTTCCT | 89848 |
| rs759083217 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | ARAP3, FCHSD1 | GRCh38.p7 | 5:141653391 | GTTGAATGAATGAAT[A/G]AGAATGGTAGTCTTT | 89848 |
| rs759094833 | in-del | -/G | 1.6575e-05 | 0.00287875 | frameshift-variant, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649448 | CCCCTGCTAGGTCAC[-/G]GTATCGGTCAGACGC | 89848 |
| rs759162383 | snp | C/G | 1.65756e-05 | 0.00287881 | splice-acceptor-variant | FCHSD1 | GRCh38.p7 | 5:141649309 | GAGGTTCTCTGTTCC[C/G]TATTGGGATGCATAC | 89848 |
| rs759186444 | snp | A/T | 4.97269e-05 | 0.00498608 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141649233 | GTTCCCGCTGCCCAT[A/T]CAGCTTCCGACTTCG | 89848 |
| rs759190176 | snp | A/G | 3.94882e-05 | 0.00444326 | intron-variant, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141639684 | GAAAGGGGGGCTGAG[A/G]TAGGGGGCCCAGTGA | 89848 |
| rs759279129 | snp | C/T | 1.79338e-05 | 0.00299443 | missense, nc-transcript-variant | FCHSD1 | GRCh38.p7 | 5:141646625 | CCATGGTTCTGGATC[C/T]TGTAGTCACGGGCAG | 89848 |
| rs759302837 | snp | C/G | 1.65181e-05 | 0.00287381 | missense, utr-variant-3-prime | RELL2, FCHSD1 | GRCh38.p7 | 5:141640168 | GCCTAACCCCTCGTG[C/G]ACTTGAAGGGAACCC | 89848 |