SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs376539391 | snp | A/G | 5.07621e-05 | 0.00503775 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231117 | CTATCTATTAACTCT[A/G]TTTTGATTTTTATTA | 89970 |
rs376543536 | snp | C/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187949 | AGCTGAAATTTTCCT[C/T]TAAGTAATTTGATCT | 89970 |
rs376547247 | snp | C/T | 3.32801e-05 | 0.00407908 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238980 | ATATTTCATGACACA[C/T]GTGAAGAGGCATCGT | 89970 |
rs376603004 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199838 | TTATCAGTGAAATTT[C/T]TTTTTTTTTTTTTTC | 89970 |
rs376611419 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219508 | CTTTTTAATCAGATT[A/G]TTGAATGTTTTCCTA | 89970 |
rs376620038 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184400 | TAGTTCCATAGAGCA[C/T]AGTGGAAATACAGAA | 89970 |
rs376714359 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216069 | CTCTGCAGGGGAATG[A/T]TTTTTTTTTTTTTTT | 89970 |
rs376837061 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200363 | CCCCACCTTTCCCCC[C/T]TTTCTATTCCACAAA | 89970 |
rs376907149 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235918 | CCAGGAATGACTCAG[C/G]CTGGGCCCCTGACTC | 89970 |
rs376980576 | in-del | -/GTTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234421 | TATTTTACTTATCTT[-/GTTT]ATTTCTGTCTTCCCC | 89970 |
rs376985451 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216088 | TTTTTTTTTTTTTTT[-/A]TCTTTTGTTGTTTTT | 89970 |
rs377043714 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221428 | CATGTGAGTACCCTA[A/G]AGAACTGTGAAAATG | 89970 |
rs377064360 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194064 | AATGAGATTCCGTTT[-/A]AAAAAAAAAAAAGAT | 89970 |
rs377153084 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228442 | CTTCTTCATTTAATG[A/G]AGCATATGATAAAGG | 89970 |
rs377179551 | snp | A/G/T | 0.000177493 | 0.00941907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227472 | TTCATTCCCTCCATT[A/G/T]TAAATTTATCAAGTG | 89970 |
rs377280141 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186948 | GAGGCATACCTCCCC[A/G]GGGAGATTTAGAAAC | 89970 |
rs377283067 | snp | A/G | | | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57212989 | TGCACTCCAGAAATT[A/G]ACTGAAATTCTCAAT | 89970 |
rs377286294 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200682 | CCCCCCACCTCCCTC[C/G]CGGACGGGGCGGCTG | 89970 |
rs377450960 | in-del | -/C | 0.0562307 | 0.157967 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200793 | CGGGCTGGGGGCTGG[-/C]CCCCCCCACATCCTT | 89970 |
rs377595245 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234013 | AGTGCGTGGCTTCTT[A/G]TTCACTGAACGGAAA | 89970 |
rs377598587 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197990 | CTCAGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 89970 |
rs377643035 | in-del | -/CT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206906 | CATAGTTATACAAAC[-/CT]CTTTGTTTTTAACTT | 89970 |
rs377648727 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202394 | TTCTCAGAAACCAGC[A/G]TAATTTATAAGATCT | 89970 |
rs377663780 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204834 | ACAGTGTTGACACCC[A/G]ACAGCAACAGGCCGA | 89970 |
rs377664761 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220717 | TTAGAAACATGAACA[C/T]TCTTTCTTTTGCAGT | 89970 |
rs397744791 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198395 | CTCAAAAAAAAAAAA[-/A]TTGTACTAAATGGAA | 89970 |
rs397839961 | in-del | -/A | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239049 | AAAAAGAAAAAAAAA[-/A]CTCTCTAATCAGTTG | 89970 |
rs397840352 | in-del | -/CT | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239054 | GAAAAAAAAAACTCT[-/CT]AATCAGTTGTACACA | 89970 |
rs397955558 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225085 | TTTGTTTTGAGACAG[-/AG]TCTCGCTCTGTCACC | 89970 |
rs527293964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236825 | AGTAAGACCTAGCAA[C/T]GCAACTGGCAGGGGG | 89970 |
rs527322936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190971 | ACTGAGAATACATTT[C/G]AAATAGTAAGGAATT | 89970 |
rs527374457 | in-del | -/GAAC | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190161 | CACTTGAGCCCAGGA[-/GAAC]GTTCAAGACCAGCCT | 89970 |
rs527496871 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194970 | CCCTAAGTTTGATTA[-/T]TTTTTTTTGTCTCAG | 89970 |
rs527572576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212908 | TGTCTCAAAAAAAAA[A/G]TGAGCCTGGGAAAAC | 89970 |
rs527623579 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207962 | TGTGTTCATTTCTTC[G/T]GTCCCTTTTTACCTC | 89970 |
rs527646305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201032 | CCCCACCTCCCTCCC[A/G]GATGGGCGGCTGGCC | 89970 |
rs527708306 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200360 | TTTCCCCACCTTTCC[A/C]CCCTTTCTATTCCAC | 89970 |
rs527711673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208226 | ACTCCAAAAATACAG[C/T]ATACATAACAATGAA | 89970 |
rs527775402 | snp | A/G | 0.000185787 | 0.00963634 | intron-variant, splice-acceptor-variant | RSPRY1 | GRCh38.p7 | 16:57207591 | TGTAGTGGTATTTCC[A/G]GAAGAAAACTTCAAA | 89970 |
rs527894977 | snp | A/G | 1.64849e-05 | 0.00287092 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213962 | GTAAGTGAGACATCA[A/G]AACTATTTATTCTTA | 89970 |
rs527900466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222972 | CAGACCTTTGGCTTG[C/T]CAAGTTAAAGACTTA | 89970 |
rs528028760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229892 | TTGTATATTTAGTAG[A/G]GATGGGGTTTCACCA | 89970 |
rs528042192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204069 | TTGTTAAATTATCCT[A/G]TGGGTTTAAAGAAAG | 89970 |
rs528042228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195992 | TCACCACTGGACTCC[A/G]GCCTGGCGACAGAGT | 89970 |
rs528099653 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229236 | CAGCATTGAGTGTCC[A/C]TTTTTCTTGTCATTG | 89970 |
rs528119304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211280 | TTAAAAAAAAAAAAA[A/G]AAAAGAAAGCCAGGC | 89970 |
rs528228474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218428 | ATGCTGTCAAATACT[A/G]GGTGTTCTTCATTCT | 89970 |
rs528310520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233976 | TAAGTCAGATCACAC[A/G]CTTCTCTGCTCAAAA | 89970 |
rs528311291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226298 | CCAGATCCCAAGAGA[A/G]GGTTTTTGGACCTCG | 89970 |
rs528425305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212543 | GATCAGATATTTCCC[A/G]TCAATGATATCATTA | 89970 |
rs528448702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201562 | AGACGGGGTGGCGGC[C/T]GGGCAGAGGCTGCAA | 89970 |
rs528482218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220402 | TATCTTATTTTATTT[A/G]TAGCTTTTGTAAATA | 89970 |
rs528630017 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198636 | CCCTGAAATTACTGA[G/T]CAACAAGATTCCTGT | 89970 |
rs528633746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235615 | CTCAGAGGGCAGCCT[A/G]GACCCTATAGAACAG | 89970 |
rs528719082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188473 | ATATCGGGCAATTTA[C/T]ATGGGATTTTTTCCG | 89970 |
rs528760344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196802 | GTTATTTCTGATTAG[A/G]TATGTGCTCATTTTG | 89970 |
rs528915304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196989 | CGTGTATCAGTAAAT[A/G]TTGCAGGGCTGGGAC | 89970 |
rs528917936 | snp | C/T | 0.000658913 | 0.018139 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204706 | GAGCAGAAGCCTTGG[C/T]CAGGGTCTGTTGTTG | 89970 |
rs529012702 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237804 | GCAACCTCCGCCTCC[C/T]GAGCTCAAGTGATTT | 89970 |
rs529060196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211425 | AAATACAAAAATTAG[C/T]CAGCACGATGGCGTG | 89970 |
rs529170629 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207483 | CCACTGAATTAAGGT[A/G]TATAATGCCACTTTG | 89970 |
rs529190427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218483 | ACCCCATTTCTCCCC[A/C]ACCCCCACTACCCTT | 89970 |
rs529234288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205596 | TCTAAATACAAAATC[A/G]TAGATTGAATAACAG | 89970 |
rs529236891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234561 | TGAACTGAATACATG[C/T]TTCATGCTTCCCTTG | 89970 |
rs529404226 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204200 | ATGCACACATCCTTC[C/T]AATGTATTTCTATAT | 89970 |
rs529452408 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215309 | AGGGCCTGAAAAGCC[A/G]GGCAGAGGGATTTAG | 89970 |
rs529595568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217416 | TCCCTCTTTACTTCT[C/T]TCCCTTTCCCAACTT | 89970 |
rs529651644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209487 | TCCTGCCTCAGCCTC[C/G]CAAGTAGCTGGGATT | 89970 |
rs529654915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225341 | CAGGCATGAGCCACT[A/G]CTCTTGGCAGCCTTG | 89970 |
rs529707255 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189054 | GCTGGAGTGCAATGG[C/T]GCGATCTCAGCTCAC | 89970 |
rs529728442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224720 | CTTCTCCTTAAATCT[A/G]TAGATGCTGCTCTGT | 89970 |
rs529801465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232323 | AACTAGAAAATGGGA[C/T]GATGATGGTAGTGTT | 89970 |
rs529806726 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223640 | AGCTGGGCGTGGTGG[C/T]GGGCGCCTGTAATCC | 89970 |
rs529829215 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219453 | TGTTTGCCATTTGTA[C/T]GTCTTCCTTTGAGAA | 89970 |
rs529847211 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186729 | TTTCGGGGGTCCTCA[C/T]CAGAAGAGGTTCTTG | 89970 |
rs529911861 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231752 | AATATTAGGAAATCT[A/T]GTACATCTTTTAGCA | 89970 |
rs529940617 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185800 | GTGTCGCCGCCAGGC[C/G]AGGACCGAGGCCGCA | 89970 |
rs529944135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193213 | CTGGGAGGCAAGTAA[A/T]AACGCCTCATCAAGA | 89970 |
rs529963896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238760 | TTTTTTTAAACCATG[C/T]ATAATTAGTAACCCT | 89970 |
rs530132346 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227232 | GCTCTCTCATCATCC[A/C]GAAAGCTTAGAATCC | 89970 |
rs530222869 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186860 | CTCAGGGGTGCCCGG[A/C/G]ATAGAAAGGGTAGAT | 89970 |
rs530260464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202086 | CAATACTTGGGAGGC[C/T]AAGATGAGAGGATTA | 89970 |
rs530281824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203010 | CCATGAATCTGTCTA[A/G]AATAATGGAAATAGG | 89970 |
rs530284507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195027 | TAGGTGCTTCATTTA[C/T]CCCCAAGAAAAATGA | 89970 |
rs530318870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209972 | TTAGCCACTGTGCCC[C/T]GCCACATTCTCTATC | 89970 |
rs530383683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210570 | CTACTAAAAATCAGC[C/T]GGGAGTGGTGGCAGG | 89970 |
rs530404754 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210245 | CCACACCTAGCTAAA[-/T]TTTTTTTTATTTTTT | 89970 |
rs530461696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195042 | CCCCCAAGAAAAATG[A/G]AAAAACATGTAAAAT | 89970 |
rs530546898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218377 | TAGTTATTTTTAAAT[A/G]TACTATAAATTATTG | 89970 |
rs530563831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225513 | TACAAAATCATTGTT[A/G]CATTCATCAGAACTT | 89970 |
rs530664667 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186746 | AGAAGAGGTTCTTGG[G/T]GGTCGCCCTTCTGAG | 89970 |
rs530723444 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186333 | GCGGGGGTGGGCTCT[G/T]CGCGTAATGGCAGCG | 89970 |
rs530732361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233079 | CAAAAATGTATATTC[A/G]GTGATACTTTATATT | 89970 |
rs530739772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224916 | CTTCTCAGGACATTA[A/G]AAGGTGAAGATAGAA | 89970 |
rs530878043 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233460 | CATTGCAACCTCCAT[C/T]TCCCAGGCTCAAGCG | 89970 |
rs530942078 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198257 | GGCGTGGTGGTGGGT[A/G]CCTGTAGTCCCAGCT | 89970 |
rs530955304 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234146 | TGCTCCTTCAGCCAC[C/G/T]CTGGCCTCCTTGCTG | 89970 |
rs531045819 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188317 | TACTTGTTAGAGATG[G/T]TTTTCCAAATATCGG | 89970 |
rs531064988 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228090 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTCATC | 89970 |
rs531066428 | in-del | -/TTTATTTTTATTTATTTA | 0.00835141 | 0.0640778 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237684 | GTATCTCTTTATTTT[-/TTTATTTTTATTTATTTA]TTTATTTTTATTTAT | 89970 |
rs531084194 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211266 | GACCTTGTCTCTGTT[-/A]AAAAAAAAAAAAAAA | 89970 |
rs531334210 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236842 | CAACTGGCAGGGGGA[C/G]TTATCTTAGGAATGC | 89970 |
rs531375224 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200236 | GGTAAGGTCACAGAT[C/G]AACAGGATCCCAAGG | 89970 |
rs531417496 | in-del | -/CGAG | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201630 | AGGTGGAGGTTGTAT[-/CGAG]CCGAGATCACGCCAC | 89970 |
rs531443399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192354 | AAAACCACAAGTACT[A/G]CGGAATATTACATTT | 89970 |
rs531502849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191192 | CTGAAGAATTGTTTT[C/T]GCTCTTGTGTTCCCT | 89970 |
rs531624194 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197822 | TCGACCTCCCAGGCT[C/G]AAGTGATCTTCCCAC | 89970 |
rs531632663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206290 | ACTTGCCTGTGATCC[C/T]AGCTACTCAGGATTC | 89970 |
rs531640360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201582 | AGAGGCTGCAATCTC[G/T]GCACTTTGGGGGGCC | 89970 |
rs531826268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201123 | CTCACTTCCCAGGCG[G/T]AGTGGCTGCCGGGCG | 89970 |
rs531895082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224004 | GCCCATGCTCCTTCC[C/T]CTGTTGAAGCATCTG | 89970 |
rs531898231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208265 | TTACTGTATGGAAAT[C/T]TCCCTGAATAGGTAT | 89970 |
rs531957821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231561 | GGGGATCTCTACCAA[A/G]TCTTTAGGTAACAGA | 89970 |
rs532036443 | in-del | -/TTTA | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237708 | ATTTATTTATTTATT[-/TTTA]TTTATTTATTTATTT | 89970 |
rs532076825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223148 | TAATGATGTTGCCAT[A/T]TTTAAAACTTTGCTT | 89970 |
rs532101452 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214113 | TTATTCCCTCCTATG[-/T]TTAAAAAAGAGAGTG | 89970 |
rs532120877 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185769 | TCATCTCTTCCGTAA[C/G]GAAGCTGGAACCCAG | 89970 |
rs532134920 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212856 | TTGACCTTGTGGTCC[A/G]CCCGCCTCGGCCTCC | 89970 |
rs532159529 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192349 | GGGGGAAAACCACAA[A/G]TACTACGGAATATTA | 89970 |
rs532163334 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186373 | CGCGTCCATCTTTGC[C/G]GTTCTCTCGGACCTG | 89970 |
rs532171843 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184709 | AACCAAGCATCACCA[C/T]TCTTGGAAGATGAAA | 89970 |
rs532207942 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226542 | TCCTTTTTAGACTAT[A/G]TAGGGTAACTTCCAA | 89970 |
rs532223535 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229501 | GCACGTGCCTGTAGT[C/T]CTAGTTACTCAGGAG | 89970 |
rs532269384 | in-del | -/TTTA | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237690 | CTTTATTTTTTTATT[-/TTTA]TTTATTTATTTATTT | 89970 |
rs532271713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200312 | GTCTACCTCTTTCTA[C/T]ACAGACATGGCAACC | 89970 |
rs532287819 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210951 | TGCAATCTGGAGGTC[A/G]AGATTGCAGTGAGAC | 89970 |
rs532308294 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185297 | ACTCTCAAGCATGAC[A/G]CTTCAACTCTCTTTG | 89970 |
rs532371743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192391 | CTTCCCTGTACTGCA[A/T]CCGTCATAAGCATTT | 89970 |
rs532440911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194637 | GTGAAGATTATAACA[A/G]TAGTAATTTAGTGCC | 89970 |
rs532522398 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192054 | TCAAAATGGTAAATA[-/T]TTTGGAGAGACTTTA | 89970 |
rs532538056 | snp | A/G | | | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240495 | ACAACTTTCATTGGT[A/G]TATACTGCTAAGGTT | 89970 |
rs532552327 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226944 | ACTGATCTTGGAATC[-/AG]AAGAATTTAGGTTCA | 89970 |
rs532577746 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186385 | TGCCGTTCTCTCGGA[C/T]CTGTCACAAAGGAGT | 89970 |
rs532599286 | in-del | -/A | 0.0133435 | 0.0805835 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226083 | AACTCCATCTCAAAG[-/A]AAAAAAAAGAAGAAA | 89970 |
rs532645775 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221712 | TTCCACCCCAGCCAC[G/T]TACTTGGCTCATTTC | 89970 |
rs532685371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216396 | ATGTTTACTCACTTT[G/T]TATAGCCAAAAATTT | 89970 |
rs532708394 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223799 | ATAAATAAATATCTT[C/T]TGCTTTTTTGTGAGT | 89970 |
rs532717013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201670 | CCAGCCTGGGCACCA[C/T]TGAGCACTGAGTGAA | 89970 |
rs532825857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189502 | CTGTGGGGCCTGGAG[A/G]CTAAAAAAAAAAAAA | 89970 |
rs532913151 | snp | A/G | 8.23662e-05 | 0.00641688 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204841 | TGACACCCAACAGCA[A/G]CAGGCCGAGAACAGT | 89970 |
rs533032919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238603 | GAAATATTATATCCC[C/T]ACCTATAAGTGCACA | 89970 |
rs533054933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205336 | TTTCATGAAGGCTCA[C/G]TGTTAATGGTACATG | 89970 |
rs533121120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219616 | TTCTGTGGGATGTCT[C/G]TTTACTTCGTTGATC | 89970 |
rs533302405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227792 | AATTGTAATGCCACT[A/G]AAATGAGGATTTTTC | 89970 |
rs533380176 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221802 | GATTCTTTTCCTTTC[A/C]AAAAATAGAGTGTTG | 89970 |
rs533395407 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184344 | TCCACAGATTCAAGA[A/T]GTCTAATAAATACCA | 89970 |
rs533458087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213789 | GCTTTAATAAGATAA[C/T]GTGCATGAAAGAGTT | 89970 |
rs533523919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222287 | GCTTTTAGAGACAGG[A/T]CTCACTGTGTTGCTC | 89970 |
rs533585532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229589 | GTACCACTGCACTCC[A/T]GCCTGGGTAATGGAG | 89970 |
rs533647915 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228729 | AGGGTCTCATCTATC[A/G]ATAGCCCAGGCTTGC | 89970 |
rs533649920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236793 | TAAATCTAAAACTCC[C/T]AAATAAAATATTAGA | 89970 |
rs533736912 | snp | C/G | 1.73586e-05 | 0.00294601 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235261 | AGGCAAAGTTTCATA[C/G]TGTTCTTAAATTGCT | 89970 |
rs533774844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188804 | TACAGGCGTGAGCCA[C/T]TGTGTCTGCCTTTCG | 89970 |
rs533782221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220923 | TGCATAGCCAGTTGT[C/T]TTAGGGCTGGTGCTT | 89970 |
rs533782283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228852 | GACACACCACCACGC[C/T]CGGCTAATTTTTGTA | 89970 |
rs533954585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189522 | AAAAAAAAAAAGTGT[C/G]TTTTGTCAAGAGTTT | 89970 |
rs534021327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190513 | AAAAGAATTATTTGG[A/G]GATAATAAACTATGG | 89970 |
rs534073554 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197317 | TACTTTGTTCATTTA[A/T]GTGCCCTGTCTGTGG | 89970 |
rs534080774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199049 | ACAAGTTTTTATAGC[A/G]TAGTGGTCAAGAAAT | 89970 |
rs534188058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237040 | GGGCGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 89970 |
rs534273457 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209510 | CTGGGATTACAGGCA[C/T]CCGCCACCACACCTG | 89970 |
rs534289019 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187024 | CTAGCGGAATGTCCT[A/G]CTACGGAAGCCGGAG | 89970 |
rs534406659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202206 | GAAACTATGAACACC[A/G]AATAAAGTAAGTGCA | 89970 |
rs534419745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205906 | TATTTTTTAAAAAGT[C/T]ACTTATGTGTTCTTT | 89970 |
rs534466544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201796 | ACCCCGTCTCCACCA[A/G]AAAAATACGAAAACC | 89970 |
rs534477683 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229576 | GTGAGCTAGGATTGT[A/G]CCACTGCACTCCAGC | 89970 |
rs534483197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213255 | GAAAATTACTGAAAG[G/T]CTACAGAGGTGAATG | 89970 |
rs534531524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209647 | GCTGGGACTACAGGC[A/G]TGAGCCACTGCACCC | 89970 |
rs534590081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216712 | GCAACAGAGTGAGAC[C/G]CTGTGACTAAAAAAA | 89970 |
rs534766086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210120 | CTTCCCCGGCCCCGC[C/T]TAGGCTAGAGTGCAG | 89970 |
rs534767335 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193288 | TCACAATCTACCCCC[C/T]TCTTACCTTCCCCAA | 89970 |
rs534785314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210950 | TTGCAATCTGGAGGT[C/T]GAGATTGCAGTGAGA | 89970 |
rs534834026 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196011 | TGGCGACAGAGTGAG[A/G]CTTCATCTCAAAAAA | 89970 |
rs534845914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218677 | GGATCTCATTCTTTT[G/T]TGTGGCTGAACAGTA | 89970 |
rs534956028 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215990 | AATGAATGAAACTTT[G/T]CTGACCACTCGAAAA | 89970 |
rs534956777 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224931 | GAAGGTGAAGATAGA[A/C]AAGAATTGCTTGCCT | 89970 |
rs534970980 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204404 | CCAAAGATAATTCTT[A/C]ATTAGAATCCTAATA | 89970 |
rs535010424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233609 | TCTTGGGTTCAAGCC[A/G]TCTGCCTGCCTCGGC | 89970 |
rs535096125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219708 | GGTGCCTGTGCTTTT[C/G]GGGTATTCAAGAAAT | 89970 |
rs535101019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234268 | TCCTCACTCCCTTTA[C/T]CTCAATATTACCTTA | 89970 |
rs535172479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196209 | AATATATGGAGCCAT[G/T]TTTTCCTTTGTGTTG | 89970 |
rs535373483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210213 | CTTCCCATGTTGCTG[A/G]ACTACAGGCATGCAC | 89970 |
rs535564819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204428 | CCTAATATCTATAAA[A/T]TCAGACTAGGAAAAT | 89970 |
rs535718013 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218937 | GAGACGGGGTTTCAC[C/T]GTTTTAGCCGGGATG | 89970 |
rs535789567 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196435 | GCCAGGTTCTGTGGT[A/G]GGTTCTATACACAGT | 89970 |
rs535791410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209836 | CATGACCCCATGTCT[A/G]GCTAATTTTGTATTT | 89970 |
rs535798380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198182 | CGAGGTCAGGAGATC[A/G]AGACTATCCTGACTA | 89970 |
rs535832405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201344 | CCGGGCAGAGACGCT[C/T]CTCACATCCCAGACG | 89970 |
rs535891727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208461 | GGAGTGCAGTGGCAC[A/G]ATCACAGCTCAACTA | 89970 |
rs536054674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223527 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 89970 |
rs536055262 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185874 | GGCGCCCACCCCAAA[C/G]CGCCACCGCAGAGCC | 89970 |
rs536182136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238001 | TGTCACCACTATGAC[C/T]TACAAAATACACAAA | 89970 |
rs536265445 | snp | C/G | 0.136166 | 0.22258 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200842 | CTGGGCAGAGGCGCC[C/G]CTCACCTCCCGGACG | 89970 |
rs536274230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192809 | CTCCCCAGCTCAGGC[A/G]ATCCTCCCACCCCTC | 89970 |
rs536381306 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232637 | TGATCCATCTAAGTT[C/T]CCATGGGGACTGGAC | 89970 |
rs536434165 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239955 | ACATGTTTTTGAATA[A/G]TTCAATCATGAATTA | 89970 |
rs536584246 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230523 | TGGCAGTATTTTTTT[C/T]TTATTGTTACATTAA | 89970 |
rs536603196 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194176 | TATTTAAGAGAAAGT[A/G]TACTGATGCCTATAG | 89970 |
rs536610380 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189892 | CACCATGCCTGGCCT[C/T]GTGAGCTTAATTTAG | 89970 |
rs536656060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225728 | TAATTTCTTAAGATC[C/T]CAGCCACCCTTTTAT | 89970 |
rs536670538 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201778 | CCCGGCCAACACAGC[A/G]AAACCCCGTCTCCAC | 89970 |
rs536716665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225090 | TTTTGAGACAGTCTC[A/G]CTCTGTCACCCAGGC | 89970 |
rs536731605 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194345 | TAGAATCTAGGTGGT[A/G]GGTATATAGTTCACA | 89970 |
rs536797195 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216636 | GAGGCGGGGGGATCA[A/C]TTGAGCCCAGTAGTT | 89970 |
rs536801762 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221763 | ATTATTACCTTGAAT[C/T]GAAGCTCTTAAGAGC | 89970 |
rs536849407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232052 | AAGTTTATCATTTTA[A/G]ACAGAGCAGCTGCCT | 89970 |
rs536856628 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215917 | AAAAATACAAGATTA[A/G]GAGAGCCTGTCCAGT | 89970 |
rs536875158 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235714 | GAGAAGAGCAGTTGG[A/G/T]CAATGTGGCGTCCTG | 89970 |
rs536879992 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | RSPRY1, FAM192A | GRCh38.p7 | 16:57186082 | AACCCAATCCGCGGA[C/G]CTCTTCCTCCCCGGG | 89970 |
rs536892332 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237639 | CTTCCATAACAATAC[A/G]AAAAACACATATATT | 89970 |
rs536942261 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193505 | GCTTTTTTTTTTTTT[A/T]CTTTGGAGACAGAGT | 89970 |
rs537129542 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190129 | TCACAACACTTTGGG[C/T]GGCCAAGGCGGGAGG | 89970 |
rs537134161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201359 | CCTCACATCCCAGAC[A/G]GGGCGGCAGGGCAGA | 89970 |
rs537248433 | in-del | -/T/TT/TTT | 0.530476 | 0.185413 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216069 | TCTGCAGGGGAATGA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 89970 |
rs537252970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233509 | CCTGAGTAGCTGGGA[C/T]TACAGGCATGCCAAC | 89970 |
rs537393655 | snp | C/T | | | missense | RSPRY1 | GRCh38.p7 | 16:57216916 | CAGGTGAAAATAAAT[C/T]GACTATTTCTGAATC | 89970 |
rs537583427 | snp | A/G | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205578 | TCCTCTGCTTTGTCT[A/G]CCTCTAAATACAAAA | 89970 |
rs537642168 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236336 | AAACTTTAGAACTAG[G/T]TATCTTAAGTATGAT | 89970 |
rs537740201 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186510 | GCGGAACGGGAGGGA[A/G]TCTGAGGGTTGGGGA | 89970 |
rs537747973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195096 | GAAATGGAGAGAATA[C/G]TCTTTAGTTTCTTTT | 89970 |
rs537849357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213429 | CAATATATAATTTGC[A/G]TATATACACACTTTA | 89970 |
rs537885105 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185463 | TCCAACCAGACGCCG[C/T]ACATCCGAGTGAGTA | 89970 |
rs537915453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222027 | CACCCAGGCCAATTG[C/G]CTTTCTTCTGATGAT | 89970 |
rs537923465 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203524 | TTTGTTTTTTTACTT[G/T]TTGCTACCAGCCCAT | 89970 |
rs537952603 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192717 | GAGACTCTTTTTTTT[C/T]TTTTTTTTTTTAAGG | 89970 |
rs537978560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228896 | GACAGGATTTTGCCA[C/T]GTTGCCCTGGCTAGT | 89970 |
rs538017897 | snp | A/G | 0.040671 | 0.13668 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200557 | CCCTGCCTCCCTCCC[A/G]GATGGGGCGGCTGGC | 89970 |
rs538069817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190348 | GGGTGACAGAGCAAC[A/G]CCCTGTCTCAAATAA | 89970 |
rs538112075 | in-del | -/GGGA/GGGG | 0.236523 | 0.250616 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228355 | TTAAATTGGTGGTGT[-/GGGA/GGGG]GGGAAAAAAATCAGA | 89970 |
rs538125897 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212052 | TGCAGTGGTTCATGC[C/T]TATAATCCCAAAACT | 89970 |
rs538133169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189598 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTGAGA | 89970 |
rs538388977 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186845 | TGGGGTCCTGACCTA[C/T]TCAGGGGTGCCCGGG | 89970 |
rs538397356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191678 | TTTACTTTTCATTGT[A/G]TGGGCAGGAATATTT | 89970 |
rs538456174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199537 | ATAATAATAGATATG[C/G]AGGCAAACATATGAA | 89970 |
rs538510108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229281 | TTGTTTATCTTTGAC[A/G]GACAAATTTGTTTAT | 89970 |
rs538518157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236900 | GGCTGGGCACGGTGG[C/T]TCACACCTGTAATCC | 89970 |
rs538558670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191414 | ACTAGAACAATATTG[G/T]AGTTTACTGTGGTCT | 89970 |
rs538583622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214042 | TGGCATAGCCACTGG[C/T]ACAGAGAATGGAATC | 89970 |
rs538647971 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239994 | GTCTTCATCAAAAGT[A/G]TTAATCCCTCTCAGG | 89970 |
rs538668575 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186974 | GAAACGCCTTGGGAT[A/G]GAGAGAGAATGGGGC | 89970 |
rs538684322 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196148 | ATCCTTAAGCAGCGT[A/T]TCATTTAGGTTCATT | 89970 |
rs538715817 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208489 | CTACAGCCTCAACCT[A/G]CCCTGGCCCAGGTGA | 89970 |
rs538765276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222604 | GCTTTTACTGTTACA[A/G]TTTCCATTTCACAGA | 89970 |
rs538792860 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239049 | AAAAAGAAAAAAAAA[A/C]CTCTCTAATCAGTTG | 89970 |
rs538793270 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212423 | TGGCATCTGAGTGGG[C/T]TTAATCTGTTTAGTG | 89970 |
rs538988994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189665 | GGTGCAATCACGGCT[C/T]ACAGAAGCCTCTACC | 89970 |
rs539015276 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235897 | GATGAACCCAGTTTG[C/T]CATCCCCAGGAATGA | 89970 |
rs539067495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227558 | TAGGAGAAGATCAAA[C/T]GTGAAAAGGGATATT | 89970 |
rs539099315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231896 | TATTTGACAAAAACT[A/G]TGATTGGCATTAATT | 89970 |
rs539188345 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185512 | ACCTCTGGAACGGAG[C/T]CTGCTACTCACTTGA | 89970 |
rs539221151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238274 | CTAAGTTTAATTTGC[G/T]CAACATAAAAAGAGC | 89970 |
rs539262639 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201271 | GTGGAGGGGCTCCTC[A/G]CTTCTCAGACGGGGC | 89970 |
rs539327288 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200818 | ATCCTTCCCGGACGG[A/G]GCGGCTGGCTGGGCA | 89970 |
rs539329655 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199433 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATCGT | 89970 |
rs539391263 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201945 | GCATCAGGGGGAGAC[C/T]GTGGAAAGAGAGAGA | 89970 |
rs539539008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198307 | GAGAATGGCATGAAC[C/T]TGGGAGGCGGAGCTT | 89970 |
rs539666166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204278 | CCTCTGGTCTATAAG[A/G]ATATGGTTTGGCAAT | 89970 |
rs539788023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220003 | TCTCTCTTCTGTTCC[A/G]TTGGTCCATGTGTCT | 89970 |
rs539984176 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199593 | GGAAAGGCATGGGCT[A/G]GGTAGAGCAGAAGAG | 89970 |
rs540005601 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206016 | CCTCAAAAATTAAGC[A/G]TAAAACAGAGTGTAC | 89970 |
rs540179657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234044 | AGCCAAAACCTTTCC[A/G]GTGACCTCCCAGGCC | 89970 |
rs540229021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221593 | ATAGAGAAATAGGAA[A/G]ACAAGTGAAATTGCC | 89970 |
rs540230566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229410 | ACTTGGGGCCAGGAG[A/T]TTGAGATTAGCCTGG | 89970 |
rs540234235 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212159 | CTCTACAGAAAATTA[A/C]AATTATCTGGGCACT | 89970 |
rs540270598 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233131 | TGGCATCAGGGTAGG[A/G]GCTCATGGCCCTGTT | 89970 |
rs540365756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227670 | CATTTCAGAAAATAA[A/T]TTTTTTACATTTGTC | 89970 |
rs540367466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219411 | TTTCTCTGATGATCA[A/G]TAATGTTGAGTACCT | 89970 |
rs540378945 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240814 | TTAATAGATAATTTG[C/T]GAGGCAAAGGAATGC | 89970 |
rs540386409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189821 | GTCTCAAACTCCTGG[A/G]CACAAGCCATCCACC | 89970 |
rs540426209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227132 | CAAAGGAGGCACTGG[A/G]AAAATATTTGTTGGT | 89970 |
rs540446611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189200 | GAGTTTCACCGTGTT[A/G]GTCAGGCTGGTCTTG | 89970 |
rs540448130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198362 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 89970 |
rs540514327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188052 | TCATACTTTCTCCCT[C/T]AGTTGTGATTTGTAA | 89970 |
rs540555687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205242 | TTCTGTAGCAGAAAA[C/T]ACGATAAAGCTATGA | 89970 |
rs540624052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232805 | TATAAATTTGGTACC[C/G]AAAGTTCGTCTTGTC | 89970 |
rs540686624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232254 | TGCAAGCAGTGCTCT[A/G]GGCTGTGCTTCACCT | 89970 |
rs540718609 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237333 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 89970 |
rs540737031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236084 | TGATTAATCCTCCCT[A/G]TTACTTCTACAGCCC | 89970 |
rs540760198 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57186208 | GGGCGGGCCGGTCCC[G/T]CTGATCACGTGACAC | 89970 |
rs540782546 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239299 | CCTTGTTGGGTTCAT[C/T]TGATTGTTTAACACA | 89970 |
rs540844522 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201494 | CAGCCAGGCAGAGAG[G/T]CTCCTCACATCCCAG | 89970 |
rs540907525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201017 | GCGGGGGGCTGACCC[C/G]CCCACCTCCCTCCCG | 89970 |
rs540908552 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206660 | CTCAGCCTCCTGGAC[C/T]CAAACCATCCTCCCA | 89970 |
rs540950169 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222233 | TCAAGCTAAACTTGC[C/T]GGCCATAAGTATGGT | 89970 |
rs540967927 | snp | C/T | 0.000676238 | 0.0183756 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204679 | CGTCTTTGGTTGGGC[C/T]GTGTTCTTAGCGAGC | 89970 |
rs540996193 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218946 | TTTCACCGTTTTAGC[C/T]GGGATGGTCTCGATC | 89970 |
rs541021853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187431 | TTTGAACTTTGAAGG[A/G]TTAGAAGTGTCTGTT | 89970 |
rs541049985 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186613 | GAAAGGGCCCGGGAG[A/C]GAGGTGGCGTTGGTC | 89970 |
rs541072153 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240317 | GCTGGATTTTTTTCC[A/G]TGTCTTTAGTCTTCC | 89970 |
rs541201633 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194753 | AGAAAAGAAAGTGTT[A/C]TTTCTCACTGATCTG | 89970 |
rs541236836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193164 | TAATGGTACTCTGTG[C/T]GACCTAAACCTACGG | 89970 |
rs541267632 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221203 | TACACTCAACCTTCC[C/T]AGTAGTCAGTTATCT | 89970 |
rs541289916 | in-del | -/TTG | 0.00199481 | 0.0315187 | utr-variant-3-prime, cds-indel | RSPRY1 | GRCh38.p7 | 16:57239925 | GAACACGTATTTCTA[-/TTG]TTCTAAATAAATACA | 89970 |
rs541312122 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210826 | AGTTCAAGACCAGCC[A/T]GGCAACATGGTGAAA | 89970 |
rs541420919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217429 | CTCTCCCTTTCCCAA[C/G]TTTGCTCTTCAAAAC | 89970 |
rs541425950 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225300 | GCCTGGCCTCAAGTG[A/G]TCTGCCCCCCAAAGT | 89970 |
rs541454810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195770 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 89970 |
rs541495034 | in-del | -/TG | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196428 | TGCTGTGCCAGGTTC[-/TG]TGTGGTAGGTTCTAT | 89970 |
rs541516306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202940 | CCATTTTTCTCTTTT[G/T]CTTCTATGTTTTCCC | 89970 |
rs541518019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225424 | TCTGAATAGTGAATA[G/T]CAATAGCTATTTCAG | 89970 |
rs541582487 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186696 | TCTGAAGAGGTTCCT[A/G]GAAGAGGGTGTTCCC | 89970 |
rs541615326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218252 | GTAATTACCACATCA[C/G]AGTAAATGGGATATC | 89970 |
rs541643387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194412 | TGGAAAATTTCATAA[C/T]AAAATATTGGGAGTG | 89970 |
rs541645673 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186309 | GAGGGAGGGCTGGGG[C/T]GGTACGAAGCGGGGG | 89970 |
rs541807785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201559 | CCCAGACGGGGTGGC[A/G]GCCGGGCAGAGGCTG | 89970 |
rs541850713 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234608 | GTACCTTCAGCAGAA[A/C]AGTTTTGCCTGTCTG | 89970 |
rs541867710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233718 | TTTCCCTGGCCATAA[C/T]CGTAGAGTATCCTTG | 89970 |
rs541883017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197475 | TAACCTCTTCTTTAC[A/T]CTTGGTTTTCACAGA | 89970 |
rs541979686 | in-del | -/TA | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208814 | TAAGATGCTTAAAAC[-/TA]TTTTAATGTGAGAGC | 89970 |
rs542020366 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199919 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTATTGAT | 89970 |
rs542064231 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239422 | ACTGGTCAGAGACAC[C/T]GGTGTGTCAAGCATG | 89970 |
rs542069121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203113 | GAGTTTGTGGCCAAC[A/G]TGGTGAAACCCCGTC | 89970 |
rs542088360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210532 | GCATGGTGAAACCCC[A/G]TCTCTACTAAAATAC | 89970 |
rs542088898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201851 | GCAATCGCAGGCACT[A/C]GGCAGGCTGAGGCAG | 89970 |
rs542151012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218331 | ATACTCTTTTGGTGT[C/T]TTAAAATTTCTTTGT | 89970 |
rs542266505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188238 | TCTTGCTTTGTAGAT[C/G]CCTCTATGAGATTGT | 89970 |
rs542285059 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207496 | GTGTATAATGCCACT[A/T]TGGAGCAATGTCTAG | 89970 |
rs542406922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207123 | TTGATTTTTGGACCT[A/G]TGTAAAAATTTATCT | 89970 |
rs542470239 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214266 | GACCTCCACAGTAGA[A/C]ACAATTACATGGCGT | 89970 |
rs542510845 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198030 | CATGCCCATCCTATC[A/G]GATTTAGTCAGATTT | 89970 |
rs542529986 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232876 | TGCTGTCTCTAGACT[A/G]TTTTCTCTGATAGTA | 89970 |
rs542549022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222186 | CCAATATGTAAGATC[C/T]TGGAATGGGTTTTAG | 89970 |
rs542663563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192127 | ATACATATTAGGGTC[C/T]AATAAGTATCCAAAT | 89970 |
rs542726880 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200147 | ATCTGTTTAACAAAG[C/T]ACATCTTGCACCACC | 89970 |
rs542763605 | in-del | -/TTAGAGTT | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229652 | CCAAAAACTGAAACC[-/TTAGAGTT]TTAGAGTTTTACTTT | 89970 |
rs542788211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199225 | AGCGGCTGGGCGCGG[C/T]GGTTGATGCCTGTAA | 89970 |
rs542810439 | snp | C/T | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205757 | TGACATTGGGTAAGT[C/T]ACTTCTTGAAGCCTC | 89970 |
rs542910315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231472 | TAAATTTCTAAGATC[A/G]CAGAAGAAATATACA | 89970 |
rs543072858 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238629 | GCACATCTGTAAGTA[C/T]ATGCTGTGCACATAT | 89970 |
rs543115088 | snp | C/T | 1.73207e-05 | 0.00294279 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216056 | GATAACTTGCCACCT[C/T]TGCAGGGGAATGATT | 89970 |
rs543175522 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215196 | TTCTTAGCTAAGGGA[A/C]CATCACAGGCAGAAG | 89970 |
rs543230011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207930 | CAGGTTGTCTCTTCT[A/C]TCTCTTTCCTTACAT | 89970 |
rs543291163 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207455 | GGACTTTTTAAAGAT[G/T]TCTGGGATCACACCA | 89970 |
rs543324569 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229167 | GAAACTTCTCTGGCA[A/G]GGGGGATATAGAATT | 89970 |
rs543326164 | snp | C/T | 0.000911914 | 0.0213337 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230829 | GTAAGTAGCTCTTCT[C/T]AGTCAAAAATTCGAG | 89970 |
rs543352620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214392 | ACTGGAATATTTAAT[A/G]TATTGTCTATGAAGC | 89970 |
rs543358013 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57186223 | GCTGATCACGTGACA[C/T]GATTTTTGAAAGGTG | 89970 |
rs543405014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194572 | TTAGCCTTTGTGGGG[A/G]AGGGTTGGAAAAAAA | 89970 |
rs543467111 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185737 | GGCCTGGCCCTAACC[C/T]TAACAGCAGCCGCAG | 89970 |
rs543618625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200261 | CCAAGGCAGAAGAAT[C/T]TTTCTTAGTACAGAA | 89970 |
rs543723451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224483 | TGTTTGTATTTGGTA[A/G]TGTTTCCATTGCTAA | 89970 |
rs543757899 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220641 | GATGCCCTTTATTTC[C/T]TCCTCTTGTCTGATT | 89970 |
rs543791434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202561 | CAATGTTGTTACTTC[A/G]ACTCTGCTGGTTTAG | 89970 |
rs543804561 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193679 | TGTATTTTTTTAAGC[-/A]AATATGTTTCTAGAT | 89970 |
rs543852918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201958 | ACCGTGGAAAGAGAG[A/G]GAGAGGGAGAGGGAG | 89970 |
rs543913863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209868 | TTTTTAGAGATGGGG[C/T]TTCATCATGTTGCCC | 89970 |
rs543920532 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195762 | GCACGGTGGCTCACA[A/C]CTGTAATCCCAGCAC | 89970 |
rs543939131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217067 | CTTTATTAAAATGTC[C/T]GTTTCCATTTCCAGA | 89970 |
rs543943782 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204745 | AGAGCACATAGCCCA[C/T]TTCCTAGGGACTGGA | 89970 |
rs543977109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209323 | GTATTGATTTTGTTA[C/T]GTAAATTTATTTTGT | 89970 |
rs544036137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216252 | TTAGTTACTGGATAA[A/G]CCTACACTTTGAACC | 89970 |
rs544045998 | in-del | -/T | 0.0711525 | 0.174681 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230005 | CACCACGCCCTGCCC[-/T]TTTTTTTTTTTTTTT | 89970 |
rs544071261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228421 | GGTTCTTGAAGGAAC[A/T]TAAAACTTCTTCATT | 89970 |
rs544105177 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209356 | TATGAAGAATTATGT[A/C]CTCTTTTTTTTTCTT | 89970 |
rs544146883 | in-del | -/T/TT | 0.481242 | 0.0950111 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189593 | TTTTCTTTTCTTTTC[-/T/TT]TTTTTTTTTTTTTTT | 89970 |
rs544152757 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192435 | CTTAGTATTTTTTGG[G/T]AGTCCAAGGCAAATT | 89970 |
rs544203797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205310 | ATGTTGCTAGCTACA[A/G]TAGGAAATGGTTTCA | 89970 |
rs544355536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221211 | ACCTTCCCAGTAGTC[A/G]GTTATCTTTGGTGGT | 89970 |
rs544357391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212252 | GGAGGTAAAGGCTAC[A/G]GTGAGCCATGATCAC | 89970 |
rs544386050 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207154 | ACAACTGTTGGGTAT[A/G]TGCATACTTAATTTT | 89970 |
rs544525824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235389 | GAAATAGAAGCAGCT[G/T]CTTGATGTGGAAGGC | 89970 |
rs544563923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199113 | CTTTAAATGCATGAG[A/G]TAGTTACATATATAC | 89970 |
rs544625041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205970 | TAAACATTTGATAAT[C/T]GCATTTATAGAAACC | 89970 |
rs544722069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229490 | CAGGGGTGGTGGCAC[G/T]TGCCTGTAGTCCTAG | 89970 |
rs544815724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236695 | AACCATAGAGAAAGT[A/G]GGAAAACCACAATGT | 89970 |
rs544816174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213543 | GTATTTAATTTGTTT[A/G]TGAATGTTACCCATT | 89970 |
rs544877889 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222161 | TTAATCTAAATAATA[C/G]CCCCCCCCTCCAATA | 89970 |
rs544929015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228464 | TGATAAAGGCCCTGT[C/T]TTCAAAAACTAGCTT | 89970 |
rs544936438 | snp | A/C | 0.195526 | 0.243993 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198383 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAATTG | 89970 |
rs544972133 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199896 | TGTTTTTTTTGTTTG[C/T]TTTTTTTTTTCTTTT | 89970 |
rs545100163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206145 | CAATGGCTCATACCT[A/G]TAATTCCAACACTTT | 89970 |
rs545188953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212855 | CTTGACCTTGTGGTC[C/T]GCCCGCCTCGGCCTC | 89970 |
rs545299023 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184809 | CACAGGGTAAGGACA[C/T]GAAGACTTCAGTTGA | 89970 |
rs545359713 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196729 | GATAAATTCTTTACT[C/T]TTCTTAGTGCTTTTA | 89970 |
rs545366606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191994 | CTCACTGCCTGCCAT[A/G]TAAGCATTGGATATA | 89970 |
rs545544244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231389 | TAAACAATTTATAAT[A/C]AACGTTAAAAGAATA | 89970 |
rs545544541 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224639 | GAGGGTGTAGGACAT[C/G]TAGGTTGTTCTCTGA | 89970 |
rs545544863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218414 | GTAGTCACCCTGTTA[C/T]GCTGTCAAATACTAG | 89970 |
rs545606612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226232 | TGAAGTCTGCTACAT[G/T]CAAGAAAGGTATTTG | 89970 |
rs545675464 | snp | A/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184355 | AAGAAGTCTAATAAA[A/T]ACCAAACAAATTGAA | 89970 |
rs545679046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237401 | ACCTGCCTTGGCCTC[C/T]GAAAAGTTCTGGGAT | 89970 |
rs545728274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236804 | CTCCCAAATAAAATA[C/T]TAGAAAGTAAGACCT | 89970 |
rs545780875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227828 | CAAGATGGCTATGGA[A/T]CAGGTCCTATCCAGT | 89970 |
rs545788034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219130 | AAACATGCGATTGCA[C/G]ATATTTCTTTGACAT | 89970 |
rs545790962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236025 | ATTTCACCCTTAGCT[A/G]TACCAGCCTCTCTTC | 89970 |
rs545841234 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211446 | CGATGGCGTGCACCT[C/G]TAATCCCAGCTACTT | 89970 |
rs545854683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235592 | AAATTTCAGTTGTAT[A/G]AGATGAACTCAGAGG | 89970 |
rs545942270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234355 | ATGTGTACACTCCTT[C/G]TCCTTCCCATTTTCC | 89970 |
rs546000445 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204575 | GCAACTTTCTTTGGC[A/G]TTCAGTTGTTAAAAA | 89970 |
rs546005785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187232 | TTGCCCGAGTGGGGT[G/T]GGGAGAGTCTATCCC | 89970 |
rs546069335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195462 | GGTTGCAGTGAGCCA[A/G]GATCACACCATTACA | 89970 |
rs546093637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196732 | AAATTCTTTACTTTT[C/T]TTAGTGCTTTTAACT | 89970 |
rs546102270 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240433 | GGTGAATACAGTAAT[C/T]TGCATTGAAGAATAA | 89970 |
rs546141489 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240455 | GAAGAATAAAACATC[G/T]GTTGCCTTTTTTGAC | 89970 |
rs546195024 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196145 | GATATCCTTAAGCAG[C/T]GTATCATTTAGGTTC | 89970 |
rs546328458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197571 | ATTTTCTTCTCTGAC[A/G]AATTTTATAGTTGAC | 89970 |
rs546477215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210154 | CACAGTCATGGCTCA[C/G]TGTATCCTCAACCTC | 89970 |
rs546505003 | snp | A/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239872 | ATACTTTGAAACTCT[A/T]GAACTAATAGTCTCA | 89970 |
rs546647899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220432 | ACAATTACTTTCTTG[A/G]TTTCTTCTTCAGATT | 89970 |
rs546815635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218433 | GTCAAATACTAGGTG[C/T]TCTTCATTCTATCTA | 89970 |
rs546871901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188578 | CTGGAGTGCAGTGGC[G/T]CTATCTCGGCTCACT | 89970 |
rs546876865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226312 | AGGGTTTTTGGACCT[C/T]GCGCAAGAAAGAATT | 89970 |
rs546887670 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229596 | TGCACTCCAGCCTGG[A/G]TAATGGAGCAAGACC | 89970 |
rs547077895 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215492 | GGGAAAGCACAGCTA[A/T]GAGAAGGTGTCATGT | 89970 |
rs547082583 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201688 | AGCACTGAGTGAACG[C/T]GACTCCGTCTGCCAT | 89970 |
rs547114144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231651 | TTTTTGTGAGATAAA[G/T]AAGATTGGTATAAAA | 89970 |
rs547217126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234785 | TGCTTGTGAGCAGAC[C/T]CTCACATATGTGATT | 89970 |
rs547292482 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185334 | AAGTTTTCTGCAAAA[C/T]GGGCCAGCTGGCTTG | 89970 |
rs547328052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200325 | TACACAGACATGGCA[A/G]CCATCCGATTTCTCA | 89970 |
rs547353755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192418 | ATTTACCTCAATTCT[C/T]CCTTAGTATTTTTTG | 89970 |
rs547463046 | in-del | -/AATG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238552 | ATGGACTGTTTGGTA[-/AATG]AATGATTCTGGGATA | 89970 |
rs547463660 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216563 | TCTCTACAAAAAATT[G/T]TAAAAAATCAGCCAG | 89970 |
rs547499930 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185446 | TCTGGGATTCAACCA[C/T]TTCCAACCAGACGCC | 89970 |
rs547514339 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210955 | ATCTGGAGGTCGAGA[C/T]TGCAGTGAGACAAGA | 89970 |
rs547524899 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185781 | TAAGGAAGCTGGAAC[C/G]CAGGTGTCGCCGCCA | 89970 |
rs547556194 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186386 | GCCGTTCTCTCGGAC[C/T]TGTCACAAAGGAGTC | 89970 |
rs547681739 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189787 | TTTAAGACAGGGTTA[C/T]GCCATGTTGCCCAGG | 89970 |
rs547697894 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212624 | GGTTATAGCTCCCCC[A/C]ACCCCCCTGAGACGG | 89970 |
rs547838706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216547 | GCATAGCAAGACTCA[A/G]TCTCTACAAAAAATT | 89970 |
rs547873600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209544 | GATTTTTGGATTTTT[A/G]GTAGAAACGGGATTT | 89970 |
rs548018429 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201686 | TGAGCACTGAGTGAA[C/T]GCGACTCCGTCTGCC | 89970 |
rs548047161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224160 | CAGGAAGTACAATAG[A/C]CGGTGTTTTAGGGAA | 89970 |
rs548066345 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185842 | GCGCGCGGGAGGCGA[A/G]ACGACCTCACCTCGG | 89970 |
rs548080672 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201286 | ACTTCTCAGACGGGG[C/T]GGTTGCCAGGCAGAG | 89970 |
rs548103844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216456 | AGTATGGTGGCTCTT[A/G]CCCATAATCCCAGCA | 89970 |
rs548126132 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185426 | TTCCCATCCTGCACT[A/G]CCATTCTGGGATTCA | 89970 |
rs548128025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193243 | ACAACCTTTCTTTTT[A/G]TGGGAAAAGTAAAAT | 89970 |
rs548141372 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231788 | GGCTTTATTGAAACA[A/G]ACTTTTTATGTGGTT | 89970 |
rs548346995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225806 | AGAAACTGCCAGGCG[C/T]GGTGGCTCACGCCTG | 89970 |
rs548347365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232369 | CACTGGCAGCAGAGC[C/T]TCAGTAATAGCCCAA | 89970 |
rs548357516 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240883 | TTGTTCCTAAGGTGG[C/G]GAGAAGACAATATAT | 89970 |
rs548410602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233452 | TCTCAGGTCATTGCA[A/G]CCTCCATCTCCCAGG | 89970 |
rs548554951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204222 | TTTCTATATAGACAG[A/G]AAAAACTATACATGT | 89970 |
rs548557245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226322 | GACCTCGCGCAAGAA[A/G]GAATTTGGGGCGAAT | 89970 |
rs548635246 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201706 | CTCCGTCTGCCATCC[C/T]GGCACCTCGGGAGGC | 89970 |
rs548687040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187489 | CCAGGCCCTTTACCT[A/G]CCATCTGTTCTTGCT | 89970 |
rs548746826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236826 | GTAAGACCTAGCAAC[A/G]CAACTGGCAGGGGGA | 89970 |
rs548754380 | in-del | -/TTTG | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203497 | CAGCTGTCAGCCTGT[-/TTTG]TTTGTTTGTTTGTTT | 89970 |
rs548822452 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218110 | GTAGCACTAACTTAT[A/T]TGTTTGTTTATTTTT | 89970 |
rs548897584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209976 | CCACTGTGCCCCGCC[A/C]CATTCTCTATCAAGG | 89970 |
rs549007922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228854 | CACACCACCACGCCC[A/G]GCTAATTTTTGTATT | 89970 |
rs549039465 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | RSPRY1 | GRCh38.p7 | 16:57213023 | AATGGAGAAGTAGCT[C/T]GCCAGGACTCAAGCC | 89970 |
rs549068024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236285 | CCTGTGGTCTTGCAC[A/G]TAATACAAGGGGTCA | 89970 |
rs549290825 | snp | A/C | 2.93088e-05 | 0.00382799 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205030 | ATCTGACTCACGGTC[A/C]CCTCCAGTGGAATGA | 89970 |
rs549370505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201066 | CGGGGGGCTGACCCC[C/G]ACCTCCCTCCCAGAC | 89970 |
rs549425111 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211720 | ACAGAGTCCTTTTTT[C/T]TTTTCTTTTTTTCTT | 89970 |
rs549487552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237746 | AGACGGAGTCTCGCT[C/T]TGTCACCCAGGCTTG | 89970 |
rs549500338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223173 | TTGCTTTAAATGTAC[A/G]TTGTTCTGGTGATTC | 89970 |
rs549563837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230871 | AATGCCCTTTTCTCT[A/G]GGAAAAAAAAAGTCT | 89970 |
rs549580748 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216432 | TGTGATTGCTAGTTT[C/T]TAGAAAAAAGTATGG | 89970 |
rs549592843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214599 | CTTACTCTCAATGAG[C/G]ACTCTGGGGATACAA | 89970 |
rs549706179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206295 | CCTGTGATCCCAGCT[A/G]CTCAGGATTCTAAGA | 89970 |
rs549716517 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186336 | GGGGTGGGCTCTGCG[A/C]GTAATGGCAGCGCCG | 89970 |
rs549717437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222443 | GGCTGTATTTCACCC[C/T]GGAATTGTTGATGGT | 89970 |
rs549778082 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185881 | ACCCCAAACCGCCAC[C/G]GCAGAGCCGCTCGCT | 89970 |
rs549801493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222545 | ACTCCTGTCTGGGGT[A/G]GAGAACTAGACCCCA | 89970 |
rs549983132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193424 | ATCAGTATTGTTGAC[A/T]TGAGATTTTCCCTAT | 89970 |
rs550044431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201138 | GAGTGGCTGCCGGGC[A/G]GAGGGGCTCCTCACT | 89970 |
rs550057573 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216824 | TAATTGCCTCTTCCC[C/T]CTCCTTAGCAATACT | 89970 |
rs550087063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198799 | TTGTTTCCCATCCCA[C/T]CTTCATACAGATTGT | 89970 |
rs550160686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193831 | AGCACTTTGGGAGGC[C/T]GAGGTGGACAGATCA | 89970 |
rs550174387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188715 | GAGACGAGGTTTCTC[C/T]GTGTTGGTCAGGCTG | 89970 |
rs550175114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231856 | CCATCAGTGAATACC[A/G]TCTTGCATAAAATTT | 89970 |
rs550185549 | snp | A/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239621 | TTTTTGGGTTTTTTT[A/T]TTTTACTGCAGAAAA | 89970 |
rs550223984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201626 | GGGGAGGTGGAGGTT[A/G]TATCGAGCCGAGATC | 89970 |
rs550320767 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189456 | ATCTGTAGTGAATCA[C/G]GTAAAAACAACAAAT | 89970 |
rs550355588 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200558 | CCTGCCTCCCTCCCG[G/T]ATGGGGCGGCTGGCC | 89970 |
rs550382171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212410 | AATGTTTTCATAATG[A/G]CATCTGAGTGGGTTT | 89970 |
rs550403646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208333 | TTTTTTTTGGCATTG[A/T]TGGATCTTTCACCAT | 89970 |
rs550458573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57207666 | GGGATTGTCGTCTCT[C/G]TTCCTGGCATTTCTC | 89970 |
rs550463967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215358 | AGAATGCTGAATAGG[C/G]TTTCCAGCAGCAGGG | 89970 |
rs550479026 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224007 | CATGCTCCTTCCCCT[C/G]TTGAAGCATCTGCCT | 89970 |
rs550480418 | in-del | -/GGACATCTAG | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224632 | CTGAGAGAGGGTGTA[-/GGACATCTAG]GGACATCTAGGTTGT | 89970 |
rs550504304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203548 | AGCCCATGTAAGTCT[C/T]CTATTTCTAAATCTT | 89970 |
rs550521220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214693 | AGGTAATTAGCCTCC[A/G]TTTTATCACAGGATG | 89970 |
rs550565184 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213755 | GGAGCTAGTACTATT[A/T]TCTACCTCAGAGCAG | 89970 |
rs550566992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205730 | TTCTGGCCCAGTGCC[C/T]TACTAACTGCATGAC | 89970 |
rs550627513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197160 | GAAACAAAAAATTGT[C/T]TAAAGTGTAATTGAT | 89970 |
rs550690932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212638 | CCACCCCCCTGAGAC[A/G]GAGCCTTGCTCTGTC | 89970 |
rs550730253 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197836 | TCAAGTGATCTTCCC[A/C]CCTCAACCTCCTGAG | 89970 |
rs550799067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211431 | AAAAATTAGCCAGCA[C/T]GATGGCGTGCACCTG | 89970 |
rs550860162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219569 | GTTATTAATCCTTTG[C/T]CGAATGGATAGTTTG | 89970 |
rs550861792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210741 | GAAGCATTTAGGTTG[A/G]GCGCAGTGGCTCACA | 89970 |
rs550887351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228678 | CTTTCCAGGTTATTA[A/G]ATAACATTACTTTTT | 89970 |
rs550910724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189399 | CATTTAGTAAGTATC[A/G]AAGGGAAATAAAAAC | 89970 |
rs551046755 | snp | A/G/T | 3.29491e-05 | 0.00405877 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204767 | GGGACTGGAGGTGCC[A/G/T]CTACTACCATGGGTA | 89970 |
rs551108350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190012 | TTTCTTTCACACTCT[A/G]TATAGTTTGGAGAAA | 89970 |
rs551146503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220516 | CCTGCAACTTTACTG[A/G]ATTTGCTTTTTAGTT | 89970 |
rs551209139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227976 | CTCTCATTTTGCTAC[C/T]CCAATCAGCATTATG | 89970 |
rs551351684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212504 | AGTGGAATCTAGTAA[A/G]TCATGTAAGGAGACT | 89970 |
rs551364651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207490 | ATTAAGGTGTATAAT[A/G]CCACTTTGGAGCAAT | 89970 |
rs551369199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199365 | GGCATGGTGGCGTGC[A/G]CCTGTAATCCCAGCT | 89970 |
rs551371679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236222 | CTGTAAGAATGTTAA[A/G]ATCTCAAACAGCTGG | 89970 |
rs551412681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220322 | TCCTCTTTGATTTCT[G/T]GCATTAGTGTTTTAT | 89970 |
rs551542607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198020 | CATGAGCCACCATGC[C/T]CATCCTATCAGATTT | 89970 |
rs551605738 | snp | C/T | 4.94214e-05 | 0.00497074 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204846 | CCCAACAGCAACAGG[C/T]CGAGAACAGTGCAGT | 89970 |
rs551619118 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213791 | TTTAATAAGATAATG[A/T]GCATGAAAGAGTTCT | 89970 |
rs551624018 | in-del | -/GTGGGCTCTGCGCGTAATGGCAGCGCC | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, cds-indel | RSPRY1, FAM192A | GRCh38.p7 | 16:57186324 | CGGTACGAAGCGGGG[-/GTGGGCTCTGCGCGTAATGGCAGCGCC]GTGGCCTCGCGTCCA | 89970 |
rs551755861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210571 | TACTAAAAATCAGCC[A/G]GGAGTGGTGGCAGGC | 89970 |
rs551761710 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202189 | AAATCTTGTCTCAGA[A/C/G]GGAAACTATGAACAC | 89970 |
rs551948754 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213211 | GAAATCTCTTAAAAA[A/T]GATATTGAGAGACAT | 89970 |
rs551977210 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191588 | AATAATGTCAGTTTT[C/T]ATCATGATTCCTCTT | 89970 |
rs552012525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221860 | CTAGTAATTAGTTGG[C/T]ATATTTTTCTCAATA | 89970 |
rs552077162 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216683 | CATAGTTGTGCCACT[C/G]CACTCCAGCCTAGGC | 89970 |
rs552125950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228745 | ATAGCCCAGGCTTGC[A/G]TGCAGTGGTGTGATC | 89970 |
rs552274570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217639 | GCAGATACCAGGTTA[A/G]GCATCCTTAATCAAA | 89970 |
rs552339576 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234164 | GGCCTCCTTGCTGCT[C/G]CTGAAACACACCAGG | 89970 |
rs552451407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233086 | GTATATTCAGTGATA[C/T]TTTATATTCATTGGA | 89970 |
rs552468705 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225319 | CCCCCCAAAGTGCTG[-/A]AAATTACAGGCATGA | 89970 |
rs552495232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203331 | AATAAAATAATGGGA[A/G]TAATATTTCTCTTCT | 89970 |
rs552532685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219619 | TGTGGGATGTCTCTT[C/T]ACTTCGTTGATCATT | 89970 |
rs552579988 | in-del | -/TTGT | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234419 | TGTATTTTACTTATC[-/TTGT]TTATTTCTGTCTTCC | 89970 |
rs552637485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195113 | CTTTAGTTTCTTTTT[A/T]AAAAAGGCAAGAATC | 89970 |
rs552681689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202229 | TAAGTGCAATTGTTA[C/T]GGGGGGTGGGTGGCG | 89970 |
rs552687659 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194364 | ATATAGTTCACAGTT[C/T]ACAGTGAACTCTAAT | 89970 |
rs552711273 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195902 | TGGCACGCACCTGTA[A/G]TCCTGGCTACTCGGG | 89970 |
rs552748823 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201799 | CCGTCTCCACCAAAA[A/G]AATACGAAAACCAGT | 89970 |
rs552766144 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186661 | CGAGAGGTTTTCCAC[C/T]GAGGCCCGCGCTTGA | 89970 |
rs552800586 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240338 | TTAGTCTTCCATAAA[G/T]CCACACACACACACA | 89970 |
rs552816470 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195953 | CTTGAACCCAGGAGA[C/T]AGAGGTTGCAGTGAG | 89970 |
rs552902178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233649 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 89970 |
rs553013142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208978 | AAAAATCTATAGACC[A/G]AAAGTCTTTCTTTTA | 89970 |
rs553091076 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204405 | CAAAGATAATTCTTC[A/T]TTAGAATCCTAATAT | 89970 |
rs553135489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218770 | AGACGGAGTCTCGCT[C/T]TGTCGCCCAGGCTGG | 89970 |
rs553196722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218288 | CCTCAAGCATTTATC[A/G]TTTATTTGTGTTAGA | 89970 |
rs553251608 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216713 | CAACAGAGTGAGACC[C/T]TGTGACTAAAAAAAA | 89970 |
rs553259948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226003 | GAATCGCTTAAACCC[A/G]GGAGGCAGAGGTTGT | 89970 |
rs553318543 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193399 | AAGTGTAATCTTCAT[A/G]CATTACCAAATCAGT | 89970 |
rs553398108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234230 | ACCCGAAACGGTTTC[C/T]CCAAACAACCACAAA | 89970 |
rs553401532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196605 | ATTCTAATGCCGTCT[A/G]TGGGATGATCAAGCT | 89970 |
rs553536250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222665 | TCATACCAGAATTCA[G/T]TGGCCTTCCTATTCT | 89970 |
rs553597501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230437 | ATTGAGCCCAAAATG[A/C]GTATTTTTCCCCACA | 89970 |
rs553608910 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214152 | ATTTATCCCAACCAG[C/G]AAAAACAGCTGAGTT | 89970 |
rs553659219 | in-del | -/G | 0.0471551 | 0.14613 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200218 | AGAGAGCACAGGGTT[-/G]GGGGTAAGGTCACAG | 89970 |
rs553792644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214771 | CGGTGGCTCATGCCT[A/G]TAAGCCCGGCATTTT | 89970 |
rs553797173 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200038 | TCTGGTTTTCCTAGG[C/T]AGAGGACCCTGCGGC | 89970 |
rs553843171 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200718 | GCAGAGGGGCTCCTC[A/T]CTTCCCAGTAGGGGC | 89970 |
rs553862966 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216028 | AGCACATATTGGGCA[A/G]GGAAATGAAACTGAT | 89970 |
rs553864847 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207074 | AAATTTTTGTTCTTA[A/C]AAACAGCACTGCAGT | 89970 |
rs553979418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222167 | TAAATAATAGCCCCC[C/G]CCTCCAATATGTAAG | 89970 |
rs554037470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236937 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACAAGG | 89970 |
rs554101579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238290 | CAACATAAAAAGAGC[A/G]ACATGATTTTTTTCT | 89970 |
rs554254506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224246 | CTCTGTTTGGGGTCA[C/T]TTGCACCATACTGAG | 89970 |
rs554286610 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185966 | AATGAAAGAAAGAAA[A/G]AAAAAAAGAAAATAG | 89970 |
rs554309252 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239079 | GTACACACATTGAAA[C/G]TTATAGCCATGGCCA | 89970 |
rs554315802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231988 | GGAAAGACTCCAGCT[A/G]CTTCCTGGTAATTAC | 89970 |
rs554333436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214853 | GGCCAACATGGCGAA[A/C]CCTGGTCCCTACTAA | 89970 |
rs554398760 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214270 | TCCACAGTAGAAACA[A/C/T]TTACATGGCGTTCCA | 89970 |
rs554415974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193460 | CACAATCTTCAGTAA[A/G]AAGATTGTGGTCTTT | 89970 |
rs554538603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200821 | CTTCCCGGACGGGGC[A/G]GCTGGCTGGGCAGAG | 89970 |
rs554552387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201353 | GACGCTCCTCACATC[C/T]CAGACGGGGCGGCAG | 89970 |
rs554586095 | in-del | -/ATT | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215944 | CAGTTCATTACTAAC[-/ATT]ATTAGCCAAATGGAT | 89970 |
rs554615686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208634 | TGTACTCCTGGGCTC[A/G]AGGGATCCTCCTGCC | 89970 |
rs554720657 | in-del | -/TTTTTG | 0.0142736 | 0.0832652 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197710 | TTAGTCAGTTTTTGT[-/TTTTTG]TTTTTGTTTTTGTTT | 89970 |
rs554720762 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221786 | TTAAGAGCTTTGTAG[A/G]GATTCTTTTCCTTTC | 89970 |
rs554752917 | snp | A/C | | | upstream-variant-2KB, missense | RSPRY1, FAM192A | GRCh38.p7 | 16:57186131 | TACCCTGAAAACGAG[A/C]CGGAGAGACTTGATT | 89970 |
rs554789109 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239973 | CAATCATGAATTATT[G/T]ACTATGTCTTCATCA | 89970 |
rs554789814 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218589 | GAGAACACACGAAGT[C/T]TGTCTTTCTGTGCCT | 89970 |
rs554843462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224350 | ACACTGTCTTCATAC[A/G]TTTCCCTTAACAGGA | 89970 |
rs554843752 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238094 | CCTTTTACCATGGTT[-/A]AAAAAAAAAGTGCTA | 89970 |
rs554865386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231013 | AGAATATTCTCTAGT[C/G]ACAGACCTGTGTGGG | 89970 |
rs554904678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232063 | TTTAAACAGAGCAGC[G/T]GCCTGTTTAAAGGGT | 89970 |
rs555001211 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187640 | TGTTGAGGAATAAAA[A/G]TGAAGGCACTTTCTA | 89970 |
rs555056635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216790 | TTTTAATTGAAGTCT[A/T]ATCTAGTCTCCAATT | 89970 |
rs555062532 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225112 | CACCCAGGCCAGGGT[G/T]CAGTGGCACGTGATC | 89970 |
rs555121158 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199715 | TAAAATACAATTTCA[A/G]GTAAATATTCCAGTG | 89970 |
rs555123783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232676 | AATGCTTCAGCATTT[A/G]GTTAACTGCTCCTGC | 89970 |
rs555253961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235950 | GCCTCTCTACGTTTG[C/T]TGTCTTTTGAAACGG | 89970 |
rs555302334 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232413 | GCATATGTTCCCGCT[C/G]AGGGTTCTGAGGTTA | 89970 |
rs555334248 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212799 | TTTGTATTCTTAGTA[C/G]AGATGGGGTTTCACC | 89970 |
rs555354048 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184652 | TGTTACTTGATTTAC[C/G]ACATACGTGGTTTTC | 89970 |
rs555384081 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222000 | ATTTCTTGCCACTTT[A/T]TACCCTTCTAACACC | 89970 |
rs555413559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191561 | TGGGGTGCATCATCT[C/G]AATTGTCTCAAAATA | 89970 |
rs555457389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220945 | CTGGTGCTTCCCACT[C/G]TCCCTGTATTTTGGA | 89970 |
rs555520135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228309 | GGAAAGCAGGAATTT[G/T]CCCACCCCCATATGG | 89970 |
rs555521115 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207012 | ATGCCTGAAAGTATT[A/G]TATTTTGTTACATTT | 89970 |
rs555538992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199053 | GTTTTTATAGCATAG[G/T]GGTCAAGAAATTATG | 89970 |
rs555581232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235316 | TTATTGTATCTAAAG[C/T]AGGCTGAATGAGGAA | 89970 |
rs555581505 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227717 | GATTAGTATGAATTC[A/T]ATTTTCCTCTTTGGA | 89970 |
rs555610442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189529 | AAAAGTGTGTTTTGT[C/T]AAGAGTTTAACAAAC | 89970 |
rs555673474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188869 | TTGTGATCCTATATT[C/T]TGTGGATCTTTTTAA | 89970 |
rs555743505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205912 | TTAAAAAGTTACTTA[C/T]GTGTTCTTTTTGCTT | 89970 |
rs555839581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236635 | CAGGTGAACTCTTTA[C/T]AACTTTCAGGGAATA | 89970 |
rs555914901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201982 | GAGGGAGAGGAGGGA[A/G]AGGGAGAGGAGCAGT | 89970 |
rs556050321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236000 | ACTTAAGGGAAGTAG[A/G]GTGTGTCTCATTTCA | 89970 |
rs556054590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205244 | CTGTAGCAGAAAACA[C/T]GATAAAGCTATGATC | 89970 |
rs556061779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228930 | AAACTTCTGGGCTCA[A/G]GTGATCCACCCAACT | 89970 |
rs556111749 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193818 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 89970 |
rs556116552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213273 | ACAGAGGTGAATGCA[A/G]TTTAATTTAGCTTTG | 89970 |
rs556170872 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212060 | TTCATGCCTATAATC[C/G]CAAAACTTTTGGGGG | 89970 |
rs556183896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214053 | CTGGCACAGAGAATG[A/G]AATCAATTGTAAATT | 89970 |
rs556184220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206031 | ATAAAACAGAGTGTA[C/G]CTGTGAATACAAACG | 89970 |
rs556258735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209912 | AACTCCTGGGCTCAA[A/G]CAGTCAGCCCACCTC | 89970 |
rs556260306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223665 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 89970 |
rs556486019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191749 | TGTTACAATGCAAAG[A/T]TAGATTCTCTAGTCC | 89970 |
rs556536884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189660 | GCAGTGGTGCAATCA[C/T]GGCTCACAGAAGCCT | 89970 |
rs556547630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199730 | AGTAAATATTCCAGT[A/G]GCACAATCATCTGAC | 89970 |
rs556614603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187751 | TTGTACTGAAAGCTT[C/T]AAGGTTCACAGCTTC | 89970 |
rs556632427 | snp | C/G | 1.65614e-05 | 0.00287757 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231333 | AGGTAAGGAATCTGC[C/G]CAGGCTATCTCCAGA | 89970 |
rs556659757 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225579 | CCATAGAAGAAGCAG[A/G]CCATCAGGACCTGAT | 89970 |
rs556660368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192743 | TAAGGTCTCACTCTG[C/T]CTCCTAGGCTGAAGT | 89970 |
rs556676139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187173 | CCTCTCTCTGTAGAT[A/C]GACCAGGTGTCCCAG | 89970 |
rs556809787 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185378 | AAAATTCGCTTGGCA[C/T]AGCAACTGGTACATG | 89970 |
rs556818930 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196330 | AGTTCATTTTACTGG[A/T]CAAGGAAATTAACAT | 89970 |
rs556830205 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187456 | TCTGTTATCGACTGA[-/G]TAGAATCCCGCAGTT | 89970 |
rs556895243 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226761 | TTTGTGACCTGTATC[G/T]TGTGCTGACCTCCTG | 89970 |
rs556931127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196601 | AGTGATTCTAATGCC[A/G]TCTATGGGATGATCA | 89970 |
rs556956731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234327 | AAATTGTTTTAATAA[C/T]ACCCCACCTCTGATG | 89970 |
rs557077934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198192 | AGATCGAGACTATCC[C/T]GACTAACACAGTGAA | 89970 |
rs557119366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195412 | AGCTATTCGGGTGGC[C/T]GAGGCAGGAGAATCG | 89970 |
rs557183307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219901 | TTTTCCAGCACCATT[C/T]ATTGAAGACACTGTC | 89970 |
rs557192264 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190398 | TATTTTTTAGTAGGA[C/T]ACTTGTAAAGTGGGG | 89970 |
rs557209416 | in-del | -/CACACACA | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240352 | ATCCACACACACACA[-/CACACACA]AAAAATATATATATA | 89970 |
rs557237955 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199226 | GCGGCTGGGCGCGGC[A/G]GTTGATGCCTGTAAT | 89970 |
rs557302739 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232171 | GACATAGCTAATGTC[A/G]GACTGGTATGCCCCT | 89970 |
rs557319100 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193957 | AATAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA | 89970 |
rs557391754 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231443 | GAGTAAAATGGATGA[A/C]TTTTCAGGAAATATA | 89970 |
rs557455340 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235952 | CTCTCTACGTTTGTT[C/G]TCTTTTGAAACGGGT | 89970 |
rs557523775 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228217 | GGCAGAGGTTGCAAT[G/T]AGCCGAGGTTGCGCC | 89970 |
rs557610887 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188776 | CTGCCTCGGCCTCCC[A/G]AAGTGCCGGGATTAC | 89970 |
rs557671932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197253 | ATGACAGCCATTTCC[A/G]GTTTAAAACCTATAG | 89970 |
rs557709895 | in-del | -/A | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239625 | GGGTTTTTTTTTTTT[-/A]ACTGCAGAAAATTGG | 89970 |
rs557834486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227559 | AGGAGAAGATCAAAT[A/G]TGAAAAGGGATATTA | 89970 |
rs557863743 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198316 | ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 89970 |
rs557875143 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190488 | CACAGTGGAACCAGC[A/G]ATCTATTTCAAAAGA | 89970 |
rs557889605 | snp | C/T | 0.000399281 | 0.0141238 | missense | RSPRY1 | GRCh38.p7 | 16:57235159 | TGAAGCAAGTCAGTA[C/T]CCGAGAAAACTGCTG | 89970 |
rs557913096 | snp | G/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240239 | CCACCCCTTCTTGTT[G/T]GTAGTTCATTATACC | 89970 |
rs557936549 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187954 | AAATTTTCCTCTAAG[A/T]AATTTGATCTCAACA | 89970 |
rs558093380 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240017 | CTCTCAGGGTCTCTG[A/G]TGAAGACCTTCAAGA | 89970 |
rs558197403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201785 | AACACAGCGAAACCC[C/T]GTCTCCACCAAAAAA | 89970 |
rs558202809 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189796 | GGGTTACGCCATGTT[A/G]CCCAGGCTGGTCTCA | 89970 |
rs558240750 | in-del | -/T | 0.00521561 | 0.0507996 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239614 | TTTTTGTTTTTTGGG[-/T]TTTTTTTTTTTACTG | 89970 |
rs558258536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209611 | TCAGGTGATCCACCT[A/G]CCTCGGCCTCCTCCC | 89970 |
rs558260688 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201428 | AGACGCTCCTCACTT[C/T]CTAGATGGGATGGCG | 89970 |
rs558273778 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | RSPRY1, FAM192A | GRCh38.p7 | 16:57186150 | AGAGACTTGATTGGG[C/T]CATTCACGCCTCAGG | 89970 |
rs558448038 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212096 | GCAGGAGGATCACTT[A/T]AGGCCAGGAGTTCAA | 89970 |
rs558511728 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206046 | CCTGTGAATACAAAC[A/G]AATTTTTAGAGCTGT | 89970 |
rs558592973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214902 | GGCATGGTGGCATGT[A/G]TGTGTAGTCCCAGCT | 89970 |
rs558769663 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215946 | GTTCATTACTAACAT[G/T]ATTAGCCAAATGGAT | 89970 |
rs558775044 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233510 | CTGAGTAGCTGGGAC[A/T]ACAGGCATGCCAACA | 89970 |
rs558834819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232786 | CTCTCTTGGTAACCA[G/T]GTATATAAATTTGGT | 89970 |
rs558868969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217153 | TCATAAGGACCTCTA[C/G]TGGCAGGTTGGATAT | 89970 |
rs558903665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225320 | CCCCCCAAAGTGCTG[A/T]AATTACAGGCATGAG | 89970 |
rs558934248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225171 | GTTCAGGCGATTCTT[A/G]TGCCTCAGCCACCAG | 89970 |
rs558957456 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238089 | AGATCCCTTTTACCA[C/T]GGTTAAAAAAAAAAG | 89970 |
rs558962437 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194209 | TACTTTGAAATATGT[-/A]AAAAAAACTGAATGG | 89970 |
rs558966796 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224630 | GAGCTGAGAGAGGGT[A/G]TAGGACATCTAGGTT | 89970 |
rs558988446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202605 | AAAAAGCTATTTCCA[C/G]CTGGTCCTTGCATCA | 89970 |
rs559015176 | in-del | -/ATAGAGTGAGACTCTGTCT | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223752 | ACTCTAGCCTGGGCG[-/ATAGAGTGAGACTCTGTCT]CAAAAATAAATAAAT | 89970 |
rs559053668 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210395 | TAGGTTAAAATTTTT[C/T]AAATGTTAAAAATAG | 89970 |
rs559064785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216475 | ATAATCCCAGCACTT[G/T]GGGAAGCTAAGGCCA | 89970 |
rs559094022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225942 | AATTAGCTGGGCCTG[G/T]TGGCGCATGCCTATA | 89970 |
rs559129270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232813 | TGGTACCCAAAGTTC[A/G]TCTTGTCTTGAATAA | 89970 |
rs559137802 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221491 | TGGTGGGTGGAAAAT[A/G]CTTATTTTTCAAATA | 89970 |
rs559183232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201550 | TCCTCACTTCCCAGA[C/T]GGGGTGGCGGCCGGG | 89970 |
rs559184995 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193210 | CATCTGGGAGGCAAG[A/T]AAAAACGCCTCATCA | 89970 |
rs559243778 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186572 | CCTGGGGCGGGCGGA[C/G]CGGACTGGGGCCGGG | 89970 |
rs559245144 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201024 | GCTGACCCCCCCACC[A/T]CCCTCCCGGATGGGC | 89970 |
rs559278935 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217386 | ACCTCTGGACCTATT[-/C]CCCTCACTTGGAATT | 89970 |
rs559281049 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185795 | CCCAGGTGTCGCCGC[A/C]AGGCCAGGACCGAGG | 89970 |
rs559302076 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195518 | ACTCCGTCTGAAAAA[A/G]TAAAAATAAAAAAGT | 89970 |
rs559316903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238758 | ATTTTTTTTAAACCA[C/T]GTATAATTAGTAACC | 89970 |
rs559429894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188927 | TTGATCTCCCAGGAT[A/G]CATGTTGCCCTAACC | 89970 |
rs559434380 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186246 | GAAAGGTGATTGGCT[A/G]TCAAGGAGAGGGCTT | 89970 |
rs559500541 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194920 | AAGACAGTGAGTACC[A/G]GAACCTTACTGCTTT | 89970 |
rs559636612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217306 | TTAATTATATGGCAC[A/T]GTCTAACCAGCTCTT | 89970 |
rs559639698 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197220 | CCATCACTTCTCTGT[-/A]AAAAAAAAATACCAT | 89970 |
rs559658470 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210855 | AACCCTGTTTCTACA[A/G]AAAAATCCAAAAGTT | 89970 |
rs559675397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210439 | TGGGCGCGGTGGTTC[A/T]CGCCTGTAATCCTAG | 89970 |
rs559686578 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212919 | AAAAATGAGCCTGGG[A/G]AAACAACCTGTGTAG | 89970 |
rs559763827 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227212 | GTATTTTCAAAAAAC[C/T]ATGAGCTCTCTCATC | 89970 |
rs559783040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187454 | TGTCTGTTATCGACT[C/G]AGTAGAATCCCGCAG | 89970 |
rs559826947 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202196 | GTCTCAGAGGGAAAC[G/T]ATGAACACCAAATAA | 89970 |
rs559862884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236812 | TAAAATATTAGAAAG[A/T]AAGACCTAGCAACGC | 89970 |
rs559879422 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231917 | GGCATTAATTTATCA[C/G]ATGAATGCCTGCTTT | 89970 |
rs559909660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194793 | TGAATGCAAGCAAAT[A/G]TTTGAAGAGATGAAT | 89970 |
rs559939077 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197808 | GGCTCACTGCAGCCT[C/T]GACCTCCCAGGCTCA | 89970 |
rs559942963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209971 | GTTAGCCACTGTGCC[C/T]CGCCACATTCTCTAT | 89970 |
rs559971171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202063 | AGGATAGCTCACACC[C/T]GTAATCCCAATACTT | 89970 |
rs560196042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221477 | TTTTTCCCCCTAGTT[A/G]GTGGGTGGAAAATAC | 89970 |
rs560251640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199179 | CATAGAGCAATATTT[A/G]TGGCTTCATTCTAGT | 89970 |
rs560277609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213550 | ATTTGTTTATGAATG[C/T]TACCCATTTTAAGAA | 89970 |
rs560314835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198558 | ATTATTCCTAAATAC[C/T]TTTATGTGTTGGCAT | 89970 |
rs560330019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207585 | TAAGCATGTAGTGGT[A/G]TTTCCAGAAGAAAAC | 89970 |
rs560372029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205428 | GCAACTTCTCTTGGC[A/G]ACATAAGGACTAAGG | 89970 |
rs560521946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208174 | AAGAAAAGTAGCCAC[C/T]TTTTGTTTTTTGTTT | 89970 |
rs560639781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222945 | GAAATTATAACTTTT[G/T]CCATGTAGTTGCAGA | 89970 |
rs560656200 | snp | A/C | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184356 | AGAAGTCTAATAAAT[A/C]CCAAACAAATTGAAC | 89970 |
rs560757657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237727 | TTTATTTATTTATTT[A/T]TTGAGACGGAGTCTC | 89970 |
rs560761989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229769 | GGAGTGCAGTGGCGC[A/G]ATCTCAGCTCACTGC | 89970 |
rs560808382 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184909 | TGTAAAAGCTGCTGT[C/T]GGCTCAATACTTTGT | 89970 |
rs560867148 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185054 | CTTATGTCACAGGTG[A/G]TAGGCAAGAGGTCAT | 89970 |
rs560867821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213674 | GTTTGGACTCTCCCA[C/T]GTGCTTGCCAAGTGC | 89970 |
rs560873423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192026 | AGTTATTGAATGGTG[G/T]TGTCTCAGTTTTTCA | 89970 |
rs560893271 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225421 | AGTCTGAATAGTGAA[-/TT]TATCAATAGCTATTT | 89970 |
rs560966516 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | RSPRY1, FAM192A | GRCh38.p7 | 16:57186037 | GTTCCTCACCGCCAC[A/T]ATAGAGTCCCGCCCC | 89970 |
rs560980831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206277 | CAGGTACAGTGGCAC[C/T]TGCCTGTGATCCCAG | 89970 |
rs560991491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191188 | CCTCCTGAAGAATTG[C/T]TTTCGCTCTTGTGTT | 89970 |
rs561065642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200177 | CCTTAATCCATTCAA[C/T]CCTGAGTGGACACAG | 89970 |
rs561181563 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201080 | CCACCTCCCTCCCAG[A/C]CGGGGTGGCTGCCGG | 89970 |
rs561238954 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208231 | AAAAATACAGCATAC[A/C]TAACAATGAAAAAAG | 89970 |
rs561385142 | snp | A/C | 1.64732e-05 | 0.0028699 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216142 | AGTCATGCTTTTTGC[A/C]CTTATCGCACTGGAA | 89970 |
rs561443365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215258 | GACAGTGTTCAGAGA[C/T]AGGACACAGACTGAG | 89970 |
rs561505572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224003 | AGCCCATGCTCCTTC[C/T]CCTGTTGAAGCATCT | 89970 |
rs561545008 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206124 | GAATAATTTTTTGGC[C/T]AGACACAATGGCTCA | 89970 |
rs561573746 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219624 | GATGTCTCTTTACTT[C/T]GTTGATCATTTCCTT | 89970 |
rs561629322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231529 | CCTAGAAAGCACCAG[A/C]CCCAGGTGGTTTCAC | 89970 |
rs561738010 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237755 | CTCGCTCTGTCACCC[A/G]GGCTTGAGTGCAGTG | 89970 |
rs561775323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204095 | GAAAGGAGTTAATTC[A/G]TTTTTTTAAAGATTT | 89970 |
rs561782681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220204 | TGAAGAATGTCATTG[A/G]TATTTTGATAGGGAT | 89970 |
rs561788251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221725 | ACGTACTTGGCTCAT[C/T]TCTTATACAGGAAGT | 89970 |
rs561809289 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215120 | TGATGAAGGTGGACC[C/G]TCAGCTGGGTCATGC | 89970 |
rs561838595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211395 | GCCAACATGGTGAAA[C/T]CTCATCTCTACTAAA | 89970 |
rs562008493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189301 | GTGCCTGGCCCTCAG[C/T]GATTATTTTCAAGTT | 89970 |
rs562046140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228637 | ATGTATATTTTTGTT[G/T]TTGTTATACTTAATA | 89970 |
rs562336540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198432 | ATAGATTATTCTGTA[C/T]TCAGTGTATAAAAAC | 89970 |
rs562410091 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234236 | AACGGTTTCTCCAAA[C/T]AACCACAAAACTTAC | 89970 |
rs562528295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206313 | CAGGATTCTAAGACC[A/G]GAGTACTGCTAGAGT | 89970 |
rs562528421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214410 | TTGTCTATGAAGCTT[C/T]TGGTTTGCTGAGGCT | 89970 |
rs562557920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197863 | TGAGTATCTGGGACC[A/G]CAGGTGTGCACTACC | 89970 |
rs562579962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220261 | GTAGTATGGACATTT[C/T]AACAATATTGAGTCT | 89970 |
rs562650791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212386 | TTTACTTCAACATCA[C/G]CAGCCTTTAATGTTT | 89970 |
rs562681762 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230220 | TTCACCATGTTGGCC[A/G]GGCTGGTCTTCAAAC | 89970 |
rs562746016 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184325 | AATTAATGAAAGACA[C/T]TAATCCACAGATTCA | 89970 |
rs562913695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229519 | AGTTACTCAGGAGGC[C/T]GAAGCAGGAGGATCA | 89970 |
rs562921369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209985 | CCCGCCACATTCTCT[A/G]TCAAGGCTTTATTTA | 89970 |
rs562950590 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222908 | AATGACCAGTGAAGC[A/T]GGATCATTTCATCTG | 89970 |
rs563068572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189903 | GCCTCGTGAGCTTAA[C/T]TTAGTCTGTTGAGAA | 89970 |
rs563101185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236786 | ATGAATATAAATCTA[A/G]AACTCCCAAATAAAA | 89970 |
rs563132721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228726 | GACAGGGTCTCATCT[A/G]TCGATAGCCCAGGCT | 89970 |
rs563164906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236145 | GTTTAGTTATCAGGG[C/T]CTCACAGACAGATGC | 89970 |
rs563165387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190676 | CAACAGCCTTTTGGA[A/G]GGGACTTTTACAACT | 89970 |
rs563176266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226191 | TCTTATCTCCAGTTT[A/T]GAAATCTCTGAATAT | 89970 |
rs563206835 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186321 | GGGCGGTACGAAGCG[G/T]GGGTGGGCTCTGCGC | 89970 |
rs563260419 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191263 | TCCACATGGGAAATA[C/T]AGCACTGTTTGTTTG | 89970 |
rs563269742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193804 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 89970 |
rs563337197 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193716 | CTCTATCTTGATAGG[A/G/T]TTTGAGTCACAGGTA | 89970 |
rs563379579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234617 | GCAGAACAGTTTTGC[C/G]TGTCTGCTTCCATTC | 89970 |
rs563396533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225494 | TTGTAATCCAAAAAT[C/G]CAGTACAAAATCATT | 89970 |
rs563511711 | snp | A/T | 0.00795532 | 0.062565 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240365 | CACACACACAAAAAA[A/T]ATATATATATATAAA | 89970 |
rs563652427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210548 | TCTCTACTAAAATAC[C/T]CCGTCTCTACTAAAA | 89970 |
rs563723141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204029 | TTTTTTAACAACAAA[C/T]GTCTGTAATTATTTT | 89970 |
rs563739601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188274 | ACTTGTGTCCCTGTA[C/T]GACATTTTACTAGTG | 89970 |
rs563801528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187521 | AGTGGAGTGACTTAA[C/T]CTCCTTAAGTCTCTA | 89970 |
rs563929482 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236412 | GACATTAAAAGAATT[A/G]TAAGAAAATTTAGCT | 89970 |
rs563962844 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203125 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 89970 |
rs564030527 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200050 | AGGCAGAGGACCCTG[C/T]GGCCTTCCACAGTGT | 89970 |
rs564110692 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228481 | TCAAAAACTAGCTTG[G/T]TTTTTAATAAGAATT | 89970 |
rs564152745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210575 | AAAAATCAGCCGGGA[C/G]TGGTGGCAGGCACCT | 89970 |
rs564172026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227849 | CCTATCCAGTGGCCA[C/T]GCTCTAAGGAAGTAG | 89970 |
rs564181307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226992 | TTGGGCAAGTAATAT[A/G]TGCTTGGGCAAGCTG | 89970 |
rs564195557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187323 | CCGTCTTTGGGGAGG[G/T]AAACCGACTGAGACC | 89970 |
rs564233694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235603 | GTATGAGATGAACTC[A/C]GAGGGCAGCCTGGAC | 89970 |
rs564257200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195522 | CGTCTGAAAAAATAA[A/G]AATAAAAAAGTATAA | 89970 |
rs564389254 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233945 | AACACAGCCTCCAGA[A/G]TGATTTGTTACAACG | 89970 |
rs564436459 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186773 | TGAGGAGGCTGCGGC[C/T]AACAGGGCCCAGGTG | 89970 |
rs564460040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204056 | TTTTATTTAAAACTT[A/G]TTAAATTATCCTATG | 89970 |
rs564477676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220370 | TCTTTCACTTCTTTG[A/T]TTAAGTTATTCCTAG | 89970 |
rs564512019 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201212 | CAGACGGTGTGGCTG[C/G]CGGGCGGAGGGGCTC | 89970 |
rs564875579 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229460 | CATCTCTATAAAAAA[A/T]TTTTAAAAATTTGCC | 89970 |
rs564880670 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234039 | GGAAAAGCCAAAACC[-/T]TTCCGGTGACCTCCC | 89970 |
rs564927056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192381 | ATTTGTTTTTCTTCC[C/T]TGTACTGCAACCGTC | 89970 |
rs564940339 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185763 | CGCAGCTCATCTCTT[C/T]CGTAAGGAAGCTGGA | 89970 |
rs564984239 | in-del | -/TTTTG | 0.0184279 | 0.0942038 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208186 | ACCTTTTGTTTTTTG[-/TTTTG]TTTTGTTTTGTTTTG | 89970 |
rs564992488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200290 | AACAAAATGAAAAGT[C/T]TCCCATGTCTACCTC | 89970 |
rs565004717 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185241 | GAACAAACAGGTCTC[C/T]CCCTTTCCTCTGTGT | 89970 |
rs565082436 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200982 | CCCCCCACCTCCCTC[C/G]CGGACGGGCGGCTGG | 89970 |
rs565148294 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186332 | AGCGGGGGTGGGCTC[G/T]GCGCGTAATGGCAGC | 89970 |
rs565398104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201644 | TCGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 89970 |
rs565443144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224073 | GGAATGATTTAGAAG[C/G]CTTTCCGGAGCCTCC | 89970 |
rs565450613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215397 | TATGTGAGGTTTCCA[C/G]AACTTAGGAGGTACC | 89970 |
rs565465744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209353 | TATTATGAAGAATTA[C/T]GTCCTCTTTTTTTTT | 89970 |
rs565504201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223504 | TTGCCTTTTGGCCAG[A/G]CGCAGTGGCTCACAC | 89970 |
rs565506171 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231751 | AAATATTAGGAAATC[A/T]AGTACATCTTTTAGC | 89970 |
rs565522856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216255 | GTTACTGGATAAGCC[C/T]ACACTTTGAACCCCA | 89970 |
rs565550069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192219 | ATATTCATGCTGCTT[A/G]TATATTTTATTTGCT | 89970 |
rs565568243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230955 | GGGAACCCATTTGAT[C/G]AGACCTAAAACTATC | 89970 |
rs565610243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210188 | GGTTCAAGTGATCCT[C/T]TTGCCTCAGCTTCCC | 89970 |
rs565643802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214806 | GGCTGAGGTGGGCTG[A/G]TCACCTGAGGTCAGG | 89970 |
rs565659742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192514 | ACTATTATTTGCTTC[C/T]GGAAATTCCTTACTC | 89970 |
rs565675788 | in-del | -/G | 0.00199481 | 0.0315187 | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240902 | AGACAATATATTTGT[-/G]GTTTATTGTAACAGA | 89970 |
rs565808651 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185826 | CCGCACTCACCTACC[A/G]GCGCGCGGGAGGCGA | 89970 |
rs565827687 | in-del | -/A | 0.0374617 | 0.131634 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226083 | ACTCCATCTCAAAGA[-/A]AAAAAAAAGAAGAAA | 89970 |
rs566001532 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186858 | TACTCAGGGGTGCCC[A/G]GGATAGAAAGGGTAG | 89970 |
rs566046399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225699 | CTGCTTCTATTTTTT[A/G]TAAGCACTCAAAATA | 89970 |
rs566108490 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196937 | CTGTTACTATGTCTG[-/T]TTTTTTAACATGTGT | 89970 |
rs566130956 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202108 | AGAGGATTATTTGAG[A/G]CTAGGAGTTCAAAAC | 89970 |
rs566223937 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239893 | AATAGTCTCAAAAAC[C/T]CTAGAGGACAGTCTG | 89970 |
rs566259098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209457 | CAACCTCCGCCTCCC[A/G]GGTCCAAGCGATTCT | 89970 |
rs566266534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194051 | ATCCTGGGCAACAGA[A/G]TGAGATTCCGTTTAA | 89970 |
rs566315194 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193303 | TTCTTACCTTCCCCA[A/G]TGAAATACCAGAGGC | 89970 |
rs566391094 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201287 | CTTCTCAGACGGGGC[A/G]GTTGCCAGGCAGAGG | 89970 |
rs566444358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228812 | ATCCTCCCACCTCAG[C/T]CTCTCCAGTAGCTGG | 89970 |
rs566457079 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238715 | TTGAGGATCAGAAAT[A/G]TAAGATTTACTTTTT | 89970 |
rs566478023 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189210 | GTGTTGGTCAGGCTG[G/T]TCTTGAACTCCTGAG | 89970 |
rs566513545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191476 | CTGGGAAACCTGGCA[C/T]CAATACAAGCTTCTC | 89970 |
rs566513600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200332 | ACATGGCAACCATCC[A/G]ATTTCTCAATCTTTT | 89970 |
rs566523301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190016 | TTTCACACTCTATAT[A/G]GTTTGGAGAAAATGT | 89970 |
rs566639969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199042 | GTTAGCCACAAGTTT[G/T]TATAGCATAGTGGTC | 89970 |
rs566929796 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198721 | AGTTATTTTTAGTAC[A/G]TGATTAGTCTCCCTT | 89970 |
rs566965233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206435 | CAAAAAAAATTTTTT[A/G]AATCCCTTGTACCAA | 89970 |
rs566996135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213216 | CTCTTAAAAATGATA[A/T]TGAGAGACATAGACT | 89970 |
rs567016015 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204280 | TCTGGTCTATAAGAA[C/T]ATGGTTTGGCAATCA | 89970 |
rs567047741 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209444 | TCTTGGCTCACTGCA[A/G]CCTCCGCCTCCCGGG | 89970 |
rs567233166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222526 | GTGGAGAGGTCAAGT[C/T]TGTACTCCTGTCTGG | 89970 |
rs567237366 | snp | G/T | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205500 | CTTATTTGACTATCT[G/T]TAATCCATTTAGGAA | 89970 |
rs567237888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228865 | GCCCGGCTAATTTTT[G/T]TATTTTTTTGGTAGA | 89970 |
rs567282370 | in-del | -/CCA | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187176 | TCTCTGTAGATCGAC[-/CCA]CAGGTGTCCCAGACA | 89970 |
rs567296359 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222023 | CTAACACCCAGGCCA[A/T]TTGGCTTTCTTCTGA | 89970 |
rs567311012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236304 | TACAAGGGGTCATTA[A/G]TGAGTGCTGAAATAT | 89970 |
rs567334707 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184418 | TGGAAATACAGAAAA[C/T]CAAACACAAAACAAT | 89970 |
rs567378102 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192711 | TTTCCAGAGACTCTT[A/T]TTTTTTTTTTTTTTT | 89970 |
rs567457240 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190290 | GGTAGAATCTCTTGA[G/T]CCTGGGAGGTTGAAG | 89970 |
rs567503437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198618 | CTTTTTGCTTTTTTT[C/T]CCCCCTGAAATTACT | 89970 |
rs567515415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231074 | TGCCAGGGTAGGATT[A/G]ACTCACCCTGCCTTT | 89970 |
rs567521350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189580 | TTTCTGTTTTTTCTT[C/T]TTCTTTTCTTTTCTT | 89970 |
rs567583621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198167 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATCG | 89970 |
rs567677990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238141 | AAGAAATATGTAGAG[C/T]GTATATGAAGAAAAC | 89970 |
rs567709039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187734 | GAGTGCTGGGAGCCA[G/T]ATTGTACTGAAAGCT | 89970 |
rs567765447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200524 | GACGGGGTGGCTGGC[C/T]GGGCGGGGGGCTGAC | 89970 |
rs567802258 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206735 | ACCTGGCTAATTTTT[A/T]AAAAAGTTTTTGTAG | 89970 |
rs567824082 | snp | C/T | 0.000185408 | 0.00962652 | intron-variant, synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57207650 | CCATAAGTCCTCAAC[C/T]GGGATTGTCGTCTCT | 89970 |
rs567896306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214627 | CAACATGGCAGTCCT[A/G]TGATTTCAAGAGGTT | 89970 |
rs567918172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211882 | CTGTGCCCAGCCTCA[A/G]TTCTGGCATTTTCAT | 89970 |
rs567963069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214034 | CAAATTGCTGGCATA[G/T]CCACTGGCACAGAGA | 89970 |
rs567999696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234251 | CAACCACAAAACTTA[C/T]TTCCTCACTCCCTTT | 89970 |
rs568077005 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203520 | TTTGTTTGTTTTTTT[A/T]CTTTTTGCTACCAGC | 89970 |
rs568145926 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196107 | ACTCATTTTCTATTC[C/T]GTTCAGTCTCTTAAC | 89970 |
rs568217134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220471 | TTGGCATATAGAAAT[A/G]CTATTGATTTTTGTC | 89970 |
rs568221741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202230 | AAGTGCAATTGTTAC[A/G]GGGGGTGGGTGGCGG | 89970 |
rs568236484 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229599 | ACTCCAGCCTGGGTA[A/G]TGGAGCAAGACCCTG | 89970 |
rs568278340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219774 | ATGTTTTATTTTAGT[A/T]GCTTCATAGTTTGAG | 89970 |
rs568388130 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215103 | ATGAAAGTCAGACTT[-/C]CTGATGAAGGTGGAC | 89970 |
rs568522907 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235878 | GGGGTCCAGAGCCTG[A/G]AGTGATGAACCCAGT | 89970 |
rs568536756 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212431 | GAGTGGGTTTAATCT[A/G]TTTAGTGATTCAAGA | 89970 |
rs568541829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211880 | CACTGTGCCCAGCCT[C/T]AATTCTGGCATTTTC | 89970 |
rs568567614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188735 | TGGTCAGGCTGGTGT[C/T]GAACTCCCGACGTCC | 89970 |
rs568605079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227928 | TCAGAGCTAGATAGA[A/G]GATATAACCCAACTC | 89970 |
rs568649817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234928 | CTATAAAATGGGAAT[G/T]GTTATACCTCCTTCA | 89970 |
rs568795743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227549 | AAAATGTCTTAGGAG[A/G]AGATCAAATGTGAAA | 89970 |
rs568823549 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235724 | GTTGGGCAATGTGGC[A/G]TCCTGGCCAGTCAAT | 89970 |
rs568828239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189472 | GTAAAAACAACAAAT[C/T]TGAGTTATGTAGCAC | 89970 |
rs568893095 | snp | A/G | 9.97241e-05 | 0.0070606 | missense | RSPRY1 | GRCh38.p7 | 16:57235132 | TACTCAGGCACAGGC[A/G]TCTTGCTCTGTTGAA | 89970 |
rs568959433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205747 | ACTAACTGCATGACA[C/T]TGGGTAAGTTACTTC | 89970 |
rs569021170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213166 | GGAAATTTGTACTGT[A/G]TGTCTTTGATCAAAC | 89970 |
rs569031997 | snp | A/C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199361 | GCCAGGCATGGTGGC[A/C/G]TGCGCCTGTAATCCC | 89970 |
rs569083856 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212683 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 89970 |
rs569121027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211432 | AAAATTAGCCAGCAC[A/G]ATGGCGTGCACCTGT | 89970 |
rs569140676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198822 | CAGATTGTATGGAAA[A/G]GCTGTGGGGTATTAG | 89970 |
rs569182899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210772 | CTTGTAATCTCAACA[A/C]TTTGGGAGGCCAAAG | 89970 |
rs569323608 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237592 | ACAGAAATGAATGGA[C/G]TAAAACAATATAAAA | 89970 |
rs569406039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221765 | TATTACCTTGAATTG[A/G]AGCTCTTAAGAGCTT | 89970 |
rs569413539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216594 | GCATGGTGGCATGCA[C/T]CTATGTTCCTAGCTA | 89970 |
rs569448297 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228019 | ATTTTTAGGCATGCT[A/C]AGAAAGCAGAAATTT | 89970 |
rs569486922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215648 | CTTAAAAACTGAGCC[A/G]TTAATTGTTAATTTA | 89970 |
rs569636153 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238113 | AAAAAAGTGCTATCT[-/AAG]AATACATAGCAAGAA | 89970 |
rs569676871 | in-del | -/TCTG | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233192 | GTGTTGTATATACTC[-/TCTG]TCTGTAATTCTTCCA | 89970 |
rs569811434 | snp | G/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187672 | AATGTAAAGTAGTAT[G/T]TAGAGGTAAGGGGTG | 89970 |
rs569813952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234121 | TTTCCTACCCTCTCC[C/T]GTTTTCTCATGCTCC | 89970 |
rs569855535 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225121 | CAGGGTGCAGTGGCA[C/T]GTGATCTCTGCTCAC | 89970 |
rs569937166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192958 | TGGGCTCAAGCTGTC[A/T]GCCTGCCTTGGCCTC | 89970 |
rs569989186 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226328 | GCGCAAGAAAGAATT[G/T]GGGGCGAATCCATAG | 89970 |
rs569992101 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239981 | AATTATTGACTATGT[C/T]TTCATCAAAAGTGTT | 89970 |
rs570100030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217963 | TTCTAGGGAATGGAA[A/G]CATAAATCTAGCAGT | 89970 |
rs570134376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225808 | AAACTGCCAGGCGCG[A/G]TGGCTCACGCCTGTA | 89970 |
rs570161558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202198 | CTCAGAGGGAAACTA[G/T]GAACACCAAATAAAG | 89970 |
rs570193066 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233474 | TCTCCCAGGCTCAAG[C/T]GATCCTCCCACCTCA | 89970 |
rs570197185 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210996 | CACTCCAGCCTGGTT[-/A]AAAAAAAGAAGTATT | 89970 |
rs570207900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195094 | TAGAAATGGAGAGAA[C/T]AGTCTTTAGTTTCTT | 89970 |
rs570218862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210117 | TTCCTTCCCCGGCCC[C/T]GCCTAGGCTAGAGTG | 89970 |
rs570223007 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201794 | AAACCCCGTCTCCAC[C/G]AAAAAAATACGAAAA | 89970 |
rs570269540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202131 | TTCAAAACCAGTCTG[A/G]GGAACATAGCAAGAC | 89970 |
rs570282041 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209616 | TGATCCACCTGCCTC[A/G]GCCTCCTCCCAAAGT | 89970 |
rs570318931 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186488 | CGCTGCTCTGAGCCC[A/T]GGGCACGCGGAACGG | 89970 |
rs570344755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194117 | ATTCGACTCCTAAAA[A/G]CTTGAAGTTTATTGA | 89970 |
rs570413811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195180 | GCAAAGGAAATATTC[G/T]ATCATAATTATGCTC | 89970 |
rs570455954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237585 | CTACAAAACAGAAAT[A/G]AATGGACTAAAACAA | 89970 |
rs570657191 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216684 | ATAGTTGTGCCACTG[C/T]ACTCCAGCCTAGGCA | 89970 |
rs570668628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226448 | CTTAGTTATTTCTCG[A/T]TTATATGCTAAACAG | 89970 |
rs570727272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211547 | GCACTTCAGCCTGGG[C/T]GACAGAGTGAGACTC | 89970 |
rs570730366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234198 | ATGATAGCTTCAGGG[C/T]ACTTGCTGTTCCTGC | 89970 |
rs570790588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219702 | TGCTTTGGTGCCTGT[A/G]CTTTTGGGGTATTCA | 89970 |
rs570858571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210882 | AGTTAACAGGGTAAC[A/G]TGGTGCATGCCTATA | 89970 |
rs571068142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230336 | TTTTTTTAAAGAAAG[A/G]CATATTTTGGGGTAG | 89970 |
rs571077419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195962 | AGGAGATAGAGGTTG[C/T]AGTGAGCCGAGATCT | 89970 |
rs571146976 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187013 | AGGAGCTAGAACTAG[A/C]GGAATGTCCTACTAC | 89970 |
rs571197079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214722 | TGTGATCATGGGAGA[A/C]AGTACTTCATCAAGA | 89970 |
rs571248083 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210700 | CCTGGGCGACAAAGC[A/G]AAACTCTGTCTCAAA | 89970 |
rs571311146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217651 | TTAAGCATCCTTAAT[C/T]AAAAAATCTGAAATC | 89970 |
rs571485652 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222841 | TCCTGATTTGGCAGC[A/G]AACACACTACAGATC | 89970 |
rs571537838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199309 | ACCAGCCTGACCAAC[A/G]TGGTGAAGATCTGTC | 89970 |
rs571572586 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186964 | GGGAGATTTAGAAAC[C/G]CCTTGGGATAGAGAG | 89970 |
rs571674855 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185890 | CGCCACCGCAGAGCC[A/G]CTCGCTCTTAAAAAA | 89970 |
rs571684442 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239750 | TAGCTGTAATGTTAG[G/T]TTGGAGAAAATTTGG | 89970 |
rs571688257 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231875 | TGCATAAAATTTTAC[A/T]GCCCTTATTTGACAA | 89970 |
rs571692918 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232148 | GCCAAGGCCAGCATA[C/T]TGGCCATGACATAGC | 89970 |
rs571732042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193446 | TTTCCCTATTTAAAC[A/G]CAATCTTCAGTAAGA | 89970 |
rs571749279 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239047 | AGAAAAAGAAAAAAA[A/T]AACTCTCTAATCAGT | 89970 |
rs571842462 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206614 | GTCACCCAGGCTGGC[A/G]TACAGTGGCGTGATC | 89970 |
rs571851565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201162 | CCTCACTTCTCAGAC[G/T]GTGTGGCTGCCAGGT | 89970 |
rs571914194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200571 | CGGATGGGGCGGCTG[A/G]CCGGGCAGAGGGGCT | 89970 |
rs571918550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208383 | GAGATTATTTATATA[C/T]ATATATATATATATA | 89970 |
rs571981803 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207738 | TCAGTTGGCACTGGG[A/C]CTCTGAGTGTAAAGC | 89970 |
rs572000372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230479 | TTGAAATTGGGATGC[A/G]TCTTAAGATTGGCTT | 89970 |
rs572047123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200825 | CCGGACGGGGCGGCT[A/G]GCTGGGCAGAGGCGC | 89970 |
rs572100136 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187201 | CAGACACAGGATCCA[A/G]CTGCTTCCGGGCTTA | 89970 |
rs572110801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200113 | GTGATGACTCTTAAC[A/G]AGCATGCTGCCTTCA | 89970 |
rs572114766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206166 | CCAACACTTTTGAGA[A/G]GCTGAGGTAGAAAGA | 89970 |
rs572177056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213611 | AGCTACTTACATCAC[A/G]TAATGTGGAAGAAAC | 89970 |
rs572236752 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185897 | GCAGAGCCGCTCGCT[C/T]TTAAAAAAGAAAAAA | 89970 |
rs572368101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209015 | ATTGATCTCGTGTGA[C/T]ATATTTTCACATTTT | 89970 |
rs572498481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216031 | ACATATTGGGCAAGG[A/C]AATGAAACTGATAAC | 89970 |
rs572499309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231998 | CAGCTGCTTCCTGGT[A/G]ATTACTTCAAGTTGA | 89970 |
rs572502062 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205169 | GATGGCAGAGTAAAT[A/G]ATAAGATTTGATGTT | 89970 |
rs572530622 | in-del | -/TTTG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218109 | GGTAGCACTAACTTA[-/TTTG]TTTGTTTATTTTTAA | 89970 |
rs572535978 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57186026 | CAGGGCTTCCTGTTC[C/T]TCACCGCCACAATAG | 89970 |
rs572560866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224293 | CCAGCTGGCCAAGCC[G/T]AGGTCATATCTTACC | 89970 |
rs572575036 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239088 | TTGAAACTTATAGCC[A/C]TGGCCAGATTTTATG | 89970 |
rs572625456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223849 | TGTGAGGTCTTTCAC[A/G]TATTTATCTTTAATC | 89970 |
rs572633945 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197161 | AAACAAAAAATTGTC[A/T]AAAGTGTAATTGATT | 89970 |
rs572665752 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184997 | TTTTATGGTGTCCCT[A/G]TGGACACATGAATAC | 89970 |
rs572699420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237651 | TACAAAAAACACATA[C/T]ATTTCAGCCAAATGC | 89970 |
rs572718520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212147 | TGAGATTCCCATCTC[C/T]ACAGAAAATTAAAAT | 89970 |
rs572781763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220012 | TGTTCCATTGGTCCA[C/T]GTGTCTGTTTTTATG | 89970 |
rs572789185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192826 | TCCTCCCACCCCTCA[C/T]TCCCACTGCCCTTCC | 89970 |
rs572966331 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227631 | ATAAATTTACCTCTG[A/G]TGGAGTTCTTCCTGT | 89970 |
rs573002346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187988 | TAAACCTCCTCCCCC[G/T]TTTGCATATATATAT | 89970 |
rs573054556 | snp | G/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184771 | ACACAATTATTCCTT[G/T]CTTATATCATGAAGC | 89970 |
rs573078639 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198324 | GGGAGGCGGAGCTTG[C/T]AGTGAGCTGAGATCA | 89970 |
rs573090653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234526 | TTGGAACAGTGCCTG[G/T]CACACAGTAAGCCCG | 89970 |
rs573103823 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187365 | CTGAGACTCCGAGGT[A/C]CTGTCTTGTATAGTT | 89970 |
rs573141545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197640 | GAAACTGACTCAAAA[C/G]ACACTTTAGTTCAAT | 89970 |
rs573143473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205217 | ACTTTGTCTGGAAAT[A/G]TCTAAATGTTTCTGT | 89970 |
rs573202512 | snp | C/T | 1.65061e-05 | 0.00287277 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204673 | AATGATCGTCTTTGG[C/T]TGGGCCGTGTTCTTA | 89970 |
rs573211657 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236522 | TCAATCCCCAGAGGA[C/G]ACTGAAAATCTAAGC | 89970 |
rs573240399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190499 | CAGCAATCTATTTCA[A/G]AAGAATTATTTGGGG | 89970 |
rs573291760 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204077 | TTATCCTATGGGTTT[A/T]AAGAAAGGAGTTAAT | 89970 |
rs573484990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212730 | AGTGATTCTCCTGCC[C/T]AAGCCTCCTGAGTAG | 89970 |
rs573523128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205261 | ATAAAGCTATGATCT[G/T]TATTAGAGAATAGAG | 89970 |
rs573609016 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206420 | CAAAAATTAATTAAT[A/C]AAAAAAAATTTTTTA | 89970 |
rs573624493 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203342 | GGGAGTAATATTTCT[C/G]TTCTAATTCCACTGA | 89970 |
rs573707156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212807 | CTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC | 89970 |
rs573731238 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228354 | GATTAAATTGGTGGT[G/T]TGGGAAAAAAATCAG | 89970 |
rs573751294 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184670 | ATACGTGGTTTTCAA[C/T]AGCTAAAGCAGCAGC | 89970 |
rs573804889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235983 | TATCTAATTGGCTGT[A/G]CACTTAAGGGAAGTA | 89970 |
rs573841193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220226 | GATAGGGATTGCATG[G/T]AATCTGTAGATTGCT | 89970 |
rs573875298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190626 | GAAAATTGAAAAGCA[A/G]AATAATCACGAAGTA | 89970 |
rs574035487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229461 | ATCTCTATAAAAAAA[A/T]TTTAAAAATTTGCCA | 89970 |
rs574090498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236638 | GTGAACTCTTTACAA[C/T]TTTCAGGGAATAGGT | 89970 |
rs574147613 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187064 | GGGTAAGGACCTTGG[A/G]GAGAGGGGATTTCTG | 89970 |
rs574158470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237144 | TGCACTCCAGCCCAG[A/G]CAAAGGCAGGTTTTT | 89970 |
rs574208975 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186686 | GCTTGAGGGATCTGA[A/G]GAGGTTCCTAGAAGA | 89970 |
rs574254308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198379 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 89970 |
rs574363280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233673 | CTGTGCCTGGCCCCT[C/T]GTCTGTTAATAACTC | 89970 |
rs574450082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232869 | AATCCTATGCTGTCT[C/T]TAGACTGTTTTCTCT | 89970 |
rs574483840 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195892 | CTGAGCGTGGTGGCA[C/T]GCACCTGTAGTCCTG | 89970 |
rs574682321 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201551 | CCTCACTTCCCAGAC[C/G]GGGTGGCGGCCGGGC | 89970 |
rs574717545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218896 | GCCCGCCACTACGCC[C/T]GGCTAATTTTTTTGT | 89970 |
rs574865380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197357 | TCAAGAGTACTCTGT[A/G]TAGTCATCTCAGAAA | 89970 |
rs574891013 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230438 | TTGAGCCCAAAATGC[A/G]TATTTTTCCCCACAT | 89970 |
rs574970493 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202229 | AAGTGCAATTGTTAC[-/G]GGGGGGTGGGTGGCG | 89970 |
rs574970728 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236231 | TGTTAAGATCTCAAA[C/T]AGCTGGATCTGGTCT | 89970 |
rs575003374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210478 | GAGGCTGAGGTGGGT[A/G]GATCACCTGAGGTCA | 89970 |
rs575029901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226034 | GGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG | 89970 |
rs575088030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218970 | CTCGATCTCCTGACC[G/T]CGTGATCCGCCCGCC | 89970 |
rs575129883 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193787 | TTTGCACATTTCAGC[C/G]GGGTGCGGTGGCTCA | 89970 |
rs575282691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226231 | TTGAAGTCTGCTACA[C/T]GCAAGAAAGGTATTT | 89970 |
rs575394298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234341 | ACACCCCACCTCTGA[C/T]GTGTACACTCCTTGT | 89970 |
rs575395175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195427 | CGAGGCAGGAGAATC[A/G]CCTGAACCGGGGAGA | 89970 |
rs575402869 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204529 | GGATGTCCAGAATCC[C/G]CTGTAGTTGATAATG | 89970 |
rs575470352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204030 | TTTTTAACAACAAAC[A/G]TCTGTAATTATTTTA | 89970 |
rs575526853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211094 | TATCTTTCTCTAAGC[A/G]ATTTCCTCATAACAA | 89970 |
rs575596260 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189150 | AGGCAAGCACCACCC[G/T]TGCCTGGCTAATTTT | 89970 |
rs575640212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198294 | GAGGCTGAGGCAGGA[A/G]AATGGCATGAACCTG | 89970 |
rs575657653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197486 | TTACACTTGGTTTTC[A/C]CAGATGGTCCTTTTT | 89970 |
rs575724038 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236458 | ACAACAATTTTAAAA[G/T]GGATATAGGGACAAA | 89970 |
rs575868736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214854 | GCCAACATGGCGAAA[A/C]CTGGTCCCTACTAAA | 89970 |
rs575892559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219963 | GTTGAAAATGAGTTC[A/C]CTGTAGATGTATGGA | 89970 |
rs575899036 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204004 | TGCTATCATATTTGT[A/G]TCATAACTTTTTTTT | 89970 |
rs576035897 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200464 | GCAGAGGGGCTCCTC[A/T]CTTCCCAGTAGGGGC | 89970 |
rs576036074 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239627 | GGTTTTTTTTTTTTA[C/T]TGCAGAAAATTGGTG | 89970 |
rs576096735 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200856 | CCCTCACCTCCCGGA[C/T]GGGGCGGCTGGCCGG | 89970 |
rs576177309 | in-del | -/TTTTG | 0.00203666 | 0.0318462 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208182 | TAGCCACCTTTTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 89970 |
rs576193602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207311 | AATGACTTAAGATGA[C/T]AGTTTTTGGGGCTTT | 89970 |
rs576256684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223602 | ACATGGTGAAACCCC[A/G]TCTCTACTGAATATA | 89970 |
rs576322378 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213539 | GCAGGTATTTAATTT[A/G]TTTATGAATGTTACC | 89970 |
rs576361190 | in-del | -/AATT | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184310 | CTGAGAATTTTACAG[-/AATT]AATGAAAGACACTAA | 89970 |
rs576368243 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239187 | ATCCCTTTTAAGGCC[A/G]AGGAAAGCTGAATGC | 89970 |
rs576447339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232226 | GCTCTTGTTTTGGCT[C/T]AAAAAGCAGATCTGC | 89970 |
rs576478021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210357 | AGTGTTGGGATTATA[C/T]GTGTAAGCCACTGTG | 89970 |
rs576542007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209849 | CTGGCTAATTTTGTA[A/T]TTTTTTTTAGAGATG | 89970 |
rs576599668 | snp | A/C | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224446 | TATTCCCTGAATGAC[A/C]AGCTGTGGATAAACT | 89970 |
rs576600802 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201461 | CGGGCAGAGACGCTC[C/T]TCACTTTCCAGACTG | 89970 |
rs576630282 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208864 | CTTTTTCCAAATAAA[A/G]GTACCCACAAATCAC | 89970 |
rs576658522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232098 | CTGTTACTAATACCA[C/T]ATATCTTATATCAGT | 89970 |
rs576660712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208908 | CTTAAGATGTTTTTA[C/T]TCCACCACGATGACT | 89970 |
rs576662707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200983 | CCCCCACCTCCCTCC[C/T]GGACGGGCGGCTGGC | 89970 |
rs576672005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216247 | TTTTCTTAGTTACTG[A/G]ATAAGCCTACACTTT | 89970 |
rs576722341 | snp | C/T | 1.64993e-05 | 0.00287218 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57208074 | GATCAGGAACCTCCC[C/T]ATTCAATGATAACAT | 89970 |
rs576748682 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186585 | GACCGGACTGGGGCC[C/G]GGGTAGGCTCTGGAA | 89970 |
rs576783958 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240236 | TTTCCACCCCTTCTT[G/T]TTTGTAGTTCATTAT | 89970 |
rs576787250 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238228 | TAGGAGGACCTCTCA[A/G]TATTGTAAAGGTGAC | 89970 |
rs576813354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194216 | AAATATGTAAAAAAA[A/C]CTGAATGGATTAATG | 89970 |
rs576821879 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57186178 | AGGATGAGGACTGGC[C/T]AGTCTGCGCCTGGAG | 89970 |
rs576826472 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, synonymous-codon | RSPRY1, FAM192A | GRCh38.p7 | 16:57186121 | GGAAATCCGGTACCC[C/T]GAAAACGAGCCGGAG | 89970 |
rs576855908 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239284 | TCACACTGGAATCCC[C/T]CTTGTTGGGTTCATT | 89970 |
rs576932727 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218758 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 89970 |
rs577052564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225970 | ATAATCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 89970 |
rs577060010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215983 | GAACTTGAATGAATG[A/G]AACTTTTCTGACCAC | 89970 |
rs577101732 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190631 | TTGAAAAGCAGAATA[A/G]TCACGAAGTAGTAAA | 89970 |
rs577111777 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193178 | GTGACCTAAACCTAC[A/G]GTTAGATAGCTTTGG | 89970 |
rs577204076 | in-del | -/AT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196032 | CTCAAAAAAAAAAAA[-/AT]AAATATATATATATA | 89970 |
rs577270059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210396 | AGGTTAAAATTTTTT[A/T]AATGTTAAAAATAGA | 89970 |
rs577281901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203841 | CATTGTGAAAATACA[A/G]CTTTTGTGATATCAG | 89970 |
rs577351608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202727 | CTGTGGTATCACTTG[A/G]CCCAGCCATTGCTGT | 89970 |
rs577396226 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217176 | TTGGATATATTCTAG[A/C]AGAAAAGTATCCTAG | 89970 |
rs577507126 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194206 | GTTTACTTTGAAATA[-/TG]TAAAAAAAACTGAAT | 89970 |
rs577539802 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199165 | TAAAAAGAGCAAATC[A/G]TAGAGCAATATTTAT | 89970 |
rs577565339 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195542 | AAAAAGTATAATCAT[A/T]TTAAAAGTATTGCCA | 89970 |
rs577595087 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195589 | AGTCCTTCTACTAAG[C/T]ACTGGCATCCAGTGA | 89970 |
rs577681066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206948 | CGAAATCTGTGTTAC[C/T]GTATATAAATCTACA | 89970 |
rs577780961 | snp | A/G | 3.30437e-05 | 0.00406457 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221450 | GTGAAAATGGGAGCA[A/G]TGGCAGTTTGCTTTT | 89970 |
rs577789490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229232 | CCACCAGCATTGAGT[A/G]TCCATTTTTCTTGTC | 89970 |
rs577801554 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184756 | AACTAAATGGTTTTG[A/C]CACAATTATTCCTTT | 89970 |
rs577806628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213506 | AAAGGAACTTCTGGT[C/T]GGAGCAGTTCCTGAG | 89970 |
rs577841951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228462 | TATGATAAAGGCCCT[A/G]TTTTCAAAAACTAGC | 89970 |
rs577962177 | snp | A/C | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185468 | CCAGACGCCGCACAT[A/C]CGAGTGAGTAACCTG | 89970 |
rs578048734 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185488 | TGAGTAACCTGGACC[C/T]GTTCCAAGACCTCTG | 89970 |
rs578205828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199758 | GACCTACTGGCCCAG[A/G]GCCAGACCTGTCCAA | 89970 |
rs745357553 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210879 | AAAAGTTAACAGGGT[A/G]ACGTGGTGCATGCCT | 89970 |
rs745358618 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226025 | AGAGGTTGTGGTGAG[C/T]CAAGATCGCGCCATT | 89970 |
rs745419640 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239333 | TGTGTTGTGTCATTC[C/T]GAAGTTTTTATTTGG | 89970 |
rs745485067 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | RSPRY1 | GRCh38.p7 | 16:57221305 | TCTTTTGAAAGTGTG[C/T]GTTGCACCTTTTGTG | 89970 |
rs745560009 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195435 | GAGAATCGCCTGAAC[C/T]GGGGAGATGGAGGTT | 89970 |
rs745564112 | snp | A/G | 5.26311e-05 | 0.0051296 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220883 | TGGACCCTTTGGGGG[A/G]TGAGAGGGTAATTAT | 89970 |
rs745595378 | snp | C/G | 1.68992e-05 | 0.00290677 | missense | RSPRY1 | GRCh38.p7 | 16:57230812 | GTCTTTTCATCTACT[C/G]TGTAAGTAGCTCTTC | 89970 |
rs745595531 | snp | A/T | 1.65737e-05 | 0.00287864 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209213 | ACTTATCTTTTATGA[A/T]ACTATCATTTGTGCT | 89970 |
rs745622818 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196688 | GAAAAGTAAAAATTA[C/G]TTCAGTACGGGGTAG | 89970 |
rs745663849 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190793 | GAGTAGAGAAAACAT[A/G]CAAATGTGTCCATTC | 89970 |
rs745666473 | in-del | -/AAAAA | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239817 | TTCTGTTTTTTTGTT[-/AAAAA]AAATTTTTTTAATCA | 89970 |
rs745706496 | snp | A/C | 7.30861e-05 | 0.00604464 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230678 | CTGGTAGTACACATC[A/C]TTATCCTAACAGTGT | 89970 |
rs745807655 | snp | C/T | 0.000979608 | 0.0221098 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239015 | TTTTTTCTACTCAAT[C/T]CCAGCCAATGTTGAA | 89970 |
rs745826354 | snp | A/T | 1.64781e-05 | 0.00287033 | missense | RSPRY1 | GRCh38.p7 | 16:57213053 | CATCCTGCCAAACAC[A/T]GGAACACATCTGCAG | 89970 |
rs745830041 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206115 | CTTCGAGAAGAATAA[C/T]TTTTTGGCCAGACAC | 89970 |
rs745849869 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222302 | TCTCACTGTGTTGCT[A/C]AGGCTGGCCTCAAAC | 89970 |
rs745884837 | in-del | -/ACAA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207073 | CAAATTTTTGTTCTT[-/ACAA]ACAGCACTGCAGTGA | 89970 |
rs746014047 | snp | A/C | 1.65195e-05 | 0.00287393 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204667 | TACCTAAATGATCGT[A/C]TTTGGTTGGGCCGTG | 89970 |
rs746020176 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186361 | GCGCCGTGGCCTCGC[A/G]TCCATCTTTGCCGTT | 89970 |
rs746108393 | snp | C/G | 9.88468e-05 | 0.00702948 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204752 | ATAGCCCACTTCCTA[C/G]GGACTGGAGGTGCCG | 89970 |
rs746110422 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192075 | AGAGACTTTATGTTA[C/G]AGATTTTAGAATAAA | 89970 |
rs746160159 | snp | C/T | 1.65982e-05 | 0.00288077 | missense | RSPRY1 | GRCh38.p7 | 16:57235135 | TCAGGCACAGGCGTC[C/T]TGCTCTGTTGAAGCA | 89970 |
rs746208063 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228401 | ACTCATTTTAATGGC[A/T]TGCAGGTTCTTGAAG | 89970 |
rs746218410 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215597 | TGCTTTCTCCTGTCT[A/G]CCATCAGCATTTGTA | 89970 |
rs746258975 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217827 | CATAACTGGACATGT[-/A]AATCCACCCCCACTG | 89970 |
rs746261539 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232081 | CTGTTTAAAGGGTAT[C/T]CCTGTTACTAATACC | 89970 |
rs746273345 | in-del | -/AG | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186546 | GTGAGGGAGGGGAAC[-/AG]CCGCTCGAGCCTGGG | 89970 |
rs746306356 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217505 | CTCTTTTCCTCCTCC[A/G]AGGGCTGCTGGGACA | 89970 |
rs746318161 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198733 | TACGTGATTAGTCTC[C/T]CTTCCTCAGGTATGT | 89970 |
rs746345987 | in-del | -/G | 1.6483e-05 | 0.00287076 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217068 | TTTATTAAAATGTCC[-/G]TTTCCATTTCCAGAC | 89970 |
rs746362986 | snp | G/T | 0.000164967 | 0.00908056 | missense | RSPRY1 | GRCh38.p7 | 16:57216951 | ATTAGTGACCGGCTT[G/T]TCACATTGGAGTCCT | 89970 |
rs746390755 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216177 | TTGCACAGACAAGTA[A/G]GTATAGTGACTTCTT | 89970 |
rs746406116 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185717 | GGGTGCGCGGACTGA[A/G]AACAGGCCTGGCCCT | 89970 |
rs746418150 | snp | G/T | 1.75065e-05 | 0.00295854 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235267 | AGTTTCATACTGTTC[G/T]TAAATTGCTAGTTCC | 89970 |
rs746472739 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237861 | GGGATTACCAGTGCC[C/T]GCCACCATGCCCAGC | 89970 |
rs746497681 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213352 | TTAAGAATAAGGAGC[A/G]AGGAAAAGAAAAAAG | 89970 |
rs746585495 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196787 | CCCCCAGGTAATTTA[A/G]TTATTTCTGATTAGA | 89970 |
rs746592167 | snp | A/G | 1.65061e-05 | 0.00287277 | missense | RSPRY1 | GRCh38.p7 | 16:57212985 | AGGATGCACTCCAGA[A/G]ATTGACTGAAATTCT | 89970 |
rs746614305 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196953 | TTTTTTAACATGTGT[C/T]AAGAGTCAGGTTAAT | 89970 |
rs746637198 | snp | C/T | 8.42496e-05 | 0.00648981 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239004 | GCATCGTGGACTTTT[C/T]TCTACTCAATTCCAG | 89970 |
rs746654099 | in-del | -/TCTC | 1.75539e-05 | 0.00296254 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227331 | ATCTTCTGGGCCTTG[-/TCTC]TCTCCAGGAAGGCTA | 89970 |
rs746679877 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215221 | CAGAAGTCCAGAGAC[-/AG]AGAATTGTCTGATGA | 89970 |
rs746745692 | snp | C/G | 1.72513e-05 | 0.0029369 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227336 | CTGGGCCTTGTCTCT[C/G]TCCAGGAAGGCTACG | 89970 |
rs746748407 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185327 | GTTTCTTAAGTTTTC[C/T]GCAAAACGGGCCAGC | 89970 |
rs746768112 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229358 | TTTAATCCCAGCACT[G/T]TTGGAGATCAAAGTG | 89970 |
rs746792923 | snp | A/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185372 | TAATAGAAAATTCGC[A/T]TGGCACAGCAACTGG | 89970 |
rs746796621 | in-del | -/AA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228274 | TGAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 89970 |
rs746845852 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187191 | CCAGGTGTCCCAGAC[A/G]CAGGATCCAACTGCT | 89970 |
rs746854440 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217805 | CATGGTTAATACTAC[A/G]CTAAAGCATAACTGG | 89970 |
rs746857986 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227881 | GTCATATGGTAGAGG[A/T]TATAACCTCTGGAAG | 89970 |
rs746858727 | snp | A/T | | | intron-variant, missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57207645 | TGCTTCCATAAGTCC[A/T]CAACCGGGATTGTCG | 89970 |
rs746884940 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223437 | ATATTTTTATGGAGG[C/T]TTAGGAGGAGCAACT | 89970 |
rs746965612 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191297 | TTTTAAGTTTTTATT[A/G]CTTCATAGTTGTTCA | 89970 |
rs746976496 | snp | A/G | 1.84831e-05 | 0.00303993 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230666 | TAGCAAAGAATCCTG[A/G]TAGTACACATCATTA | 89970 |
rs746991547 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185381 | ATTCGCTTGGCACAG[-/CA]ACTGGTACATGGCAC | 89970 |
rs746993215 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209553 | ATTTTTAGTAGAAAC[A/G]GGATTTCACCATGTT | 89970 |
rs746995380 | snp | A/G | 1.69109e-05 | 0.00290778 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208148 | TACTTTATAATGAAT[A/G]TATAATAATGAAGAA | 89970 |
rs747010905 | in-del | -/GGG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200948 | ACGGGGCGGCTGGCC[-/GGG]GGGGGGGGGGGCTGA | 89970 |
rs747014682 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216152 | TTTGCACTTATCGCA[C/T]TGGAAAAGTTTGCAC | 89970 |
rs747061454 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202076 | CCCGTAATCCCAATA[C/T]TTGGGAGGCCAAGAT | 89970 |
rs747112933 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205876 | TGTACTTAACAGTTG[C/T]TCAGTAGATGGTAGT | 89970 |
rs747176689 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215972 | TGGATAATTGAGAAC[C/T]TGAATGAATGAAACT | 89970 |
rs747198781 | snp | C/T | 0.000116133 | 0.00761927 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204654 | GAAAACTGAAAACTA[C/T]CTAAATGATCGTCTT | 89970 |
rs747200285 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234061 | TGACCTCCCAGGCCC[C/T]GTACAATTTGTCCTC | 89970 |
rs747249060 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234008 | ATGCCAGTGCGTGGC[-/T]TCTTATTCACTGAAC | 89970 |
rs747255939 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216890 | TAATTCAAGGATTAT[A/G]TCTTTCCAAACAGGT | 89970 |
rs747352436 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202654 | TCAGTCACATCCTTT[C/T]CAGTACAACCTCCAA | 89970 |
rs747398427 | snp | A/G | 1.66518e-05 | 0.00288542 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205051 | AGTGGAATGAAAAGT[A/G]TTCTGCCCGGAACCA | 89970 |
rs747404412 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230298 | ATTACAGGCGTGAGC[C/T]ACCTCGCCCAGCCTG | 89970 |
rs747484457 | snp | C/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187227 | GCTTATTGCCCGAGT[C/G]GGGTGGGGAGAGTCT | 89970 |
rs747506824 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57231287 | TAATGACTACGCCTT[C/T]CTAACAGCTGAAGAA | 89970 |
rs747534450 | snp | A/C | 1.66554e-05 | 0.00288573 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57235128 | TTTCTACTCAGGCAC[A/C]GGCGTCTTGCTCTGT | 89970 |
rs747558535 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225180 | ATTCTTGTGCCTCAG[C/G]CACCAGAGTAACTGG | 89970 |
rs747731427 | snp | A/G | 1.66843e-05 | 0.00288823 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208134 | AGTTTTGTTTTCATT[A/G]CTTTATAATGAATAT | 89970 |
rs747733488 | in-del | -/TGTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191269 | TGGGAAATATAGCAC[-/TGTT]TGTTTGTTTTTTTAA | 89970 |
rs747744979 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222827 | ATAAAACTTGTCTCT[C/T]CTGATTTGGCAGCAA | 89970 |
rs747819229 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57209166 | AACATTGTTACTAGA[C/T]GAATGTCCATTGCCC | 89970 |
rs747834588 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223719 | AGAGGTTGCACTGAG[C/G]CCAGATAGTGCCACT | 89970 |
rs747914840 | in-del | -/CTTTTTC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199907 | TTTGTTTTTTTTTTT[-/CTTTTTC]TTTTTTTTTTTTTTT | 89970 |
rs747922486 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209798 | TCCCACCTCAGCCTC[C/G]CATGTAGCTGGGACC | 89970 |
rs748008831 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210583 | GCCGGGAGTGGTGGC[A/G]GGCACCTGTAATCCC | 89970 |
rs748015760 | snp | A/C | 7.30861e-05 | 0.00604464 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227318 | GGCAGACTTGCTAAT[A/C]TTCTGGGCCTTGTCT | 89970 |
rs748149573 | snp | A/G | 6.58924e-05 | 0.0057395 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57221346 | GGTATGGTACTATGA[A/G]GTAACAGTGGTCACT | 89970 |
rs748175636 | snp | C/G | 1.64819e-05 | 0.00287066 | missense | RSPRY1 | GRCh38.p7 | 16:57231268 | CTATGAAATTTAGCA[C/G]TTTTAATGACTACGC | 89970 |
rs748249857 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217671 | AATCTGAAATCCTCC[A/G]TTGAGCATTTCCTTT | 89970 |
rs748256592 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219464 | TGTATGTCTTCCTTT[A/G]AGAAATGTCTATTCG | 89970 |
rs748284644 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237742 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG | 89970 |
rs748290189 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232681 | TTCAGCATTTAGTTA[A/G]CTGCTCCTGCAGAAT | 89970 |
rs748374354 | in-del | -/GTA | 1.67677e-05 | 0.00289544 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212931 | GGGAAAACAACCTGT[-/GTA]GTATATGGGTCAAAC | 89970 |
rs748389895 | snp | C/T | 5.1754e-05 | 0.00508668 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220876 | CTACAGTTGGACCCT[C/T]TGGGGGATGAGAGGG | 89970 |
rs748408537 | snp | A/G | 1.78902e-05 | 0.00299078 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235097 | CCCTGTTGACAAAAT[A/G]TATTTCAAATTGCTT | 89970 |
rs748483051 | snp | C/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187448 | TAGAAGTGTCTGTTA[C/T]CGACTGAGTAGAATC | 89970 |
rs748581287 | snp | C/G | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204768 | GGACTGGAGGTGCCG[C/G]TACTACCATGGGTAA | 89970 |
rs748672051 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239171 | TGCCAGCCCTGAGAA[A/G]ATCCCTTTTAAGGCC | 89970 |
rs748673463 | snp | A/G | 0.000148296 | 0.00860964 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204891 | CAAGGAGCCAACCAC[A/G]GGACCCTGTTCGGCC | 89970 |
rs748718384 | in-del | -/AA | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239040 | GTTGAAAAGAAAAAG[-/AA]AAAAAAAACTCTCTA | 89970 |
rs748741112 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223874 | TTAATCTTTTTGAGA[A/G]TTTGGAAAGGTATTA | 89970 |
rs748788581 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224869 | CATGGTGGCTAGCTT[C/T]TAGGAATTTCTTTCA | 89970 |
rs748790254 | in-del | -/TATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202883 | TTACATATGATTATA[-/TATA]TATATATATATATAT | 89970 |
rs748971344 | snp | C/T | | | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240615 | TCCAGCAGATTGTTA[C/T]TGAGCACCTAATATG | 89970 |
rs748986400 | snp | G/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239472 | TGAATCTATAAAAAT[G/T]AGAATCACACAGTCA | 89970 |
rs749013008 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211788 | TCTTGCTATGTTGCC[C/T]AGACTGGTCTCAAAC | 89970 |
rs749017946 | in-del | -/GAA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222800 | GATTCTTCCAGGGAG[-/GAA]GAAGCTTCGATATAA | 89970 |
rs749181866 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193139 | TTCTTGACAGTTACA[G/T]TTCAGGAGTTAATGG | 89970 |
rs749247069 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232511 | TTGGCCAAAGTCTGA[A/G]GGGACACCTCTCCCT | 89970 |
rs749275831 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219649 | TTCCTTTGCTGTAAG[A/G]AACTTTTTAGCTTAA | 89970 |
rs749337238 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230885 | TAGGAAAAAAAAAGT[A/C]TTTGTCCATTTATAT | 89970 |
rs749352606 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223705 | GGAATATGGGAGGCA[-/G]AGGTTGCACTGAGCC | 89970 |
rs749364175 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221070 | AAGAATGGCTGCAAA[C/G]AATTCTTTGATTCTG | 89970 |
rs749389994 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204889 | CACAAGGAGCCAACC[A/G]CGGGACCCTGTTCGG | 89970 |
rs749404318 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205971 | AAACATTTGATAATC[A/G]CATTTATAGAAACCC | 89970 |
rs749449469 | snp | A/G | 1.65751e-05 | 0.00287876 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213102 | AGAAACTAGCAGGTA[A/G]CTTTGGGACACTCCA | 89970 |
rs749506219 | snp | A/G | 3.2962e-05 | 0.00405954 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57231251 | ATTCAAATACCCACC[A/G]TCTATGAAATTTAGC | 89970 |
rs749594884 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237239 | GCCTCTGCCTCCTGG[C/G]TTCATGCAATTCTCC | 89970 |
rs749630529 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197654 | ACACACTTTAGTTCA[A/G]TTTGGAAAAAAACTT | 89970 |
rs749631307 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191005 | GTACTCCTTAAATTT[A/G]TTAAGGAATGAACTC | 89970 |
rs749685578 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199261 | GCACTTTGGTAGGCC[A/G]AGGCGGGCGGATCAC | 89970 |
rs749775195 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204764 | CTAGGGACTGGAGGT[A/G]CCGCTACTACCATGG | 89970 |
rs749819622 | snp | C/T | 1.66054e-05 | 0.00288139 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220715 | CCTTAGAAACATGAA[C/T]ACTCTTTCTTTTGCA | 89970 |
rs749829252 | in-del | -/T | 0.113508 | 0.209452 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216070 | TCTGCAGGGGAATGA[-/T]TTTTTTTTTTTTTTT | 89970 |
rs749843370 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196962 | ATGTGTCAAGAGTCA[A/G]GTTAATTAGGACGTG | 89970 |
rs749874678 | in-del | -/CTAA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232917 | ATAGTTGTCAGGAGC[-/CTAA]CTGAGTGGCCACCTT | 89970 |
rs749897516 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189120 | TGCCTCAGCCTCCCA[A/G]GTAACTGGGATTACA | 89970 |
rs749897761 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206774 | CTTGCCATGTTGCCC[A/G]GGCTGGTCTCAAATA | 89970 |
rs749993678 | snp | G/T | 0.288649 | 0.246995 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216095 | TTTTTTTTATCTTTT[G/T]TTGTTTTTCAGAAGT | 89970 |
rs750031557 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227280 | GTCGTAAAAGACACA[A/C]TCTCTGTTCCCAGGT | 89970 |
rs750063097 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233459 | TCATTGCAACCTCCA[G/T]CTCCCAGGCTCAAGC | 89970 |
rs750180468 | in-del | -/AATG | 1.70133e-05 | 0.00291657 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208155 | TAATGAATATATAAT[-/AATG]AAGAAAAGTAGCCAC | 89970 |
rs750199476 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232126 | AGTAAGAGAGTCTCT[C/T]TCAGCAGCCAAGGCC | 89970 |
rs750238834 | snp | A/G | 1.92829e-05 | 0.00310501 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204994 | ACTGGCAGTAATACG[A/G]ACTCTTGTAGATAAG | 89970 |
rs750262878 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212136 | GGCAACATAATGAGA[-/T]TTCCCATCTCTACAG | 89970 |
rs750293863 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197780 | ATAGGCTGGAATGCA[A/T]TGACACCATTAGGGC | 89970 |
rs750331517 | snp | A/G | 3.29544e-05 | 0.00405908 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57213934 | AATACTGGAATACTT[A/G]CTACAGTGTCTGGTA | 89970 |
rs750335152 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199360 | AGCCAGGCATGGTGG[C/T]GTGCGCCTGTAATCC | 89970 |
rs750339442 | in-del | -/ATC | 0.062739 | 0.16563 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216088 | TTTTTTTTTTTTTTT[-/ATC]TTTTGTTGTTTTTCA | 89970 |
rs750366013 | snp | A/C | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185184 | TTTTAAAAGGGCCCC[A/C]GGAGATCTTGTTTTC | 89970 |
rs750422966 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57186224 | CTGATCACGTGACAC[A/G]ATTTTTGAAAGGTGA | 89970 |
rs750535080 | snp | C/T | 3.39443e-05 | 0.00411959 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220682 | GCACTAGCTTCTTCT[C/T]TTCTCCACAGCAGCC | 89970 |
rs750573817 | snp | A/T | 4.98235e-05 | 0.00499092 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221255 | TAGTTGATTGACACA[A/T]TTTTTGGTTTTGCCA | 89970 |
rs750613608 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195763 | CACGGTGGCTCACAC[A/C]TGTAATCCCAGCACT | 89970 |
rs750655344 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237434 | CAGGCATGAGTCACC[A/G]TGCCCAGCCTACAAT | 89970 |
rs750672550 | snp | G/T | 1.65089e-05 | 0.00287301 | missense | RSPRY1 | GRCh38.p7 | 16:57220830 | GAGTACCTGAAGATC[G/T]CACCTCATGGCTTAG | 89970 |
rs750777640 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193621 | CCTCAGCCTCCCAAG[C/T]AGCTGGAATTACAGG | 89970 |
rs750796926 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189505 | TGGGGCCTGGAGGCT[-/A]AAAAAAAAAAAAGTG | 89970 |
rs750823953 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230199 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 89970 |
rs750867569 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194408 | TGTTTGGAAAATTTC[A/G]TAATAAAATATTGGG | 89970 |
rs750879821 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57209154 | ACCAGCTGTTATAAC[A/G]TTGTTACTAGATGAA | 89970 |
rs750904281 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216496 | GCTAAGGCCAGAGCA[C/T]TGCTTCAGGCCAGGA | 89970 |
rs750949856 | snp | A/C | 3.29451e-05 | 0.00405851 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238978 | TCATATTTCATGACA[A/C]ATGTGAAGAGGCATC | 89970 |
rs750952622 | in-del | -/CTGGAGGTG | | | cds-indel, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204755 | CCCACTTCCTAGGGA[-/CTGGAGGTG]CTGGAGGTGCCGCTA | 89970 |
rs750976640 | snp | A/G | 1.67156e-05 | 0.00289093 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212947 | TAGTATATGGGTCAA[A/G]CCCACTTGTACTTTT | 89970 |
rs751026332 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191881 | AAGAGGCCTCCTTCT[A/G]GTAGATGCTTTATCT | 89970 |
rs751056831 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239382 | GATGTAAATGACAGC[A/G]TTTCTGGGTTATGCA | 89970 |
rs751120638 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203956 | GCTTCCAATGGGAAA[C/T]TCTATCCTTTTATTC | 89970 |
rs751136149 | snp | A/T | 3.31549e-05 | 0.0040714 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231158 | CCTCTGTACTCATTT[A/T]ATTTGTAGATCTGGA | 89970 |
rs751186955 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214595 | TTACCTTACTCTCAA[G/T]GAGCACTCTGGGGAT | 89970 |
rs751202450 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236730 | TTTAGTAATCATACC[-/A]AAAGCTGATAAAACT | 89970 |
rs751226269 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230459 | TTCCCCACATTTTAA[C/T]ATCTTTGAAATTGGG | 89970 |
rs751304551 | in-del | -/GAAAA | 7.93226e-05 | 0.00629722 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239028 | ATTCCAGCCAATGTT[-/GAAAA]GAAAAAGAAAAAAAA | 89970 |
rs751350046 | in-del | -/CAG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223981 | CTAGAGATTTCAGGC[-/CAG]CAGGATAGCCCATGC | 89970 |
rs751429057 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186328 | ACGAAGCGGGGGTGG[A/G]CTCTGCGCGTAATGG | 89970 |
rs751454522 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203875 | TCCTTTCCCAAAACA[A/C]AGCCTTGCTTACATA | 89970 |
rs751455985 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186945 | GATGAGGCATACCTC[C/T]CCGGGGAGATTTAGA | 89970 |
rs751456874 | snp | A/G | 1.64814e-05 | 0.00287061 | missense | RSPRY1 | GRCh38.p7 | 16:57220801 | GGGCCATGCTGAATA[A/G]CAATGATGTCAGCGA | 89970 |
rs751473704 | snp | A/C | 3.34102e-05 | 0.00408705 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57230799 | TCCTGAAAAGCAAGT[A/C]TTTTCATCTACTGTG | 89970 |
rs751524635 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224369 | CCCTTAACAGGAAAC[A/G]GTTGGGATGCCCTAC | 89970 |
rs751535632 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238570 | TGATTCTGGGATAAA[A/T]GGCTAGCTTTCTGGG | 89970 |
rs751548928 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204807 | TCTGCCGAGATGACA[A/G]TGGAACAGATGACAG | 89970 |
rs751564701 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210459 | TGTAATCCTAGCACT[C/T]TGGGAGGCTGAGGTG | 89970 |
rs751612887 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225381 | TTTCTAAGGCAATTA[C/G]ATGCAAGCTCATTTA | 89970 |
rs751680836 | in-del | -/TA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188961 | TATTTAATGTCTTTC[-/TA]TGTTATGCTTTTTTC | 89970 |
rs751699743 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198722 | GTTATTTTTAGTACG[-/T]GATTAGTCTCCCTTC | 89970 |
rs751729712 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190259 | AGATAGTCCCAGCTA[C/G]TTGGGAGGCTGAGGT | 89970 |
rs751785104 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57238942 | TCGTAAAGAAATAGT[A/G]TCTAGAATCAGACAG | 89970 |
rs751923070 | in-del | -/AT | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240365 | ACACACACAAAAAAT[-/AT]ATATATATATATAAA | 89970 |
rs751947373 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228158 | CCCACCTGCGGTCCC[A/G]GCTACTTGGGAGGCT | 89970 |
rs752011882 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215166 | TATTGTGCCCAGAGG[A/C]GGGAAAAAATTGGTT | 89970 |
rs752021465 | snp | C/T | 1.73652e-05 | 0.00294657 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227459 | TGGAAAGAAGGTATT[C/T]ATTCCCTCCATTATA | 89970 |
rs752027861 | snp | C/G | 1.65078e-05 | 0.00287291 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221444 | AGAACTGTGAAAATG[C/G]GAGCAGTGGCAGTTT | 89970 |
rs752053805 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209725 | GTCACCCAGGCTGGC[A/G]TGCAGTAGAGCAATC | 89970 |
rs752077531 | snp | A/G | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205605 | AAAATCATAGATTGA[A/G]TAACAGTGAAATTAA | 89970 |
rs752118169 | snp | A/T | 6.60557e-05 | 0.0057466 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208041 | TCAGGTTTAATGCCT[A/T]GAATTTTTTTTTCCA | 89970 |
rs752215504 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218233 | TGATACAGTCATACA[A/G]TGAGTAATTACCACA | 89970 |
rs752228227 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217094 | CAGACTCATTTCTTT[C/T]ATAGGCTCACTGGTC | 89970 |
rs752303602 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203933 | GAATTCTGTCAGTTC[C/T]TGAGTGAGCTTCCAA | 89970 |
rs752322548 | snp | C/G | 1.90271e-05 | 0.00308435 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227499 | AGTGGGTTAAGACAT[C/G]TGGTTATTATGAGGC | 89970 |
rs752364013 | snp | C/T | 1.66272e-05 | 0.00288328 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212960 | AAACCCACTTGTACT[C/T]TTTTGTTTTAGGATG | 89970 |
rs752370599 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217215 | AGACAAGAATTACAT[-/G]GGTATGCTTCTAATT | 89970 |
rs752476637 | snp | C/T | 1.65143e-05 | 0.00287348 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57238883 | TTTCTCCCCAGTGAC[C/T]TGTGCATGGATTGTG | 89970 |
rs752561960 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225749 | ACCCTTTTATTTTAA[C/T]AGTTCTGTGAAATAA | 89970 |
rs752589447 | snp | A/G | 1.69037e-05 | 0.00290716 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204619 | AATTCCTCAACTCCA[A/G]GTTATGAAAACAGTA | 89970 |
rs752591763 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57235217 | CACACAATTGAAGCC[A/G]TGTGGACACAGGTAA | 89970 |
rs752603547 | snp | A/T | 1.65037e-05 | 0.00287256 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216875 | CTACCCTTTCATTGT[A/T]AATTCAAGGATTATG | 89970 |
rs752604673 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236820 | TAGAAAGTAAGACCT[A/C]GCAACGCAACTGGCA | 89970 |
rs752631025 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199023 | TCCCCAAAGTGTTAG[G/T]TGGGTTAGCCACAAG | 89970 |
rs752636895 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204699 | TCTTAGCGAGCAGAA[C/G]CCTTGGCCAGGGTCT | 89970 |
rs752649920 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211589 | CAACAACAAAAAAAA[G/T]TTAAAACTGAAAGCA | 89970 |
rs752691519 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217043 | CAATCTCTGTAAGTG[A/G]GAGTTGTCCTTTATT | 89970 |
rs752742026 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212762 | TGGGATTACAGGCGC[C/G]CACCACCACACCTGG | 89970 |
rs752831843 | snp | C/G | 1.65359e-05 | 0.00287536 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208025 | GTCATTTATTATTTC[C/G]TCAGGTTTAATGCCT | 89970 |
rs752876271 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196383 | CTTTAGTATTTCAGT[G/T]TGCCCCCTAGTTCAG | 89970 |
rs752889172 | in-del | -/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184516 | GAGTGAAACATAATA[-/T]TTAAGAATGAAGACA | 89970 |
rs752922796 | in-del | -/C | 0.00157491 | 0.0280174 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216090 | TTTTTTTTTTTTTAT[-/C]TTTTGTTGTTTTTCA | 89970 |
rs753066069 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207047 | CTGGTGATGGTCACT[C/T]AGGTTACTGCCAAAT | 89970 |
rs753074202 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240121 | TCAGCAGCTGCCTTT[C/T]AATTTATGCCAAGTC | 89970 |
rs753112705 | snp | C/G/T | 3.29969e-05 | 0.00406172 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221434 | AGTACCCTAGAGAAC[C/G/T]GTGAAAATGGGAGCA | 89970 |
rs753143873 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209265 | CAAAGAACATTTGAT[G/T]TATTGTGTTTCATCT | 89970 |
rs753171443 | snp | G/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240209 | ACTCAATGCACATTT[G/T]TTTTTCTTCTTTTTC | 89970 |
rs753202334 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199907 | TTTGTTTTTTTTTTT[-/C]TTTTTCTTTTTTTTT | 89970 |
rs753266908 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57221280 | TTGCCAGGCTCGCTG[C/T]GATGCCTCCTCTTTT | 89970 |
rs753316859 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220103 | GATTCCTCCAGTTTC[A/G]TTTTCTTGCTGAGGG | 89970 |
rs753347753 | snp | A/G | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205469 | TTTTCATTATCCTTT[A/G]TTTGATCCTTTATCC | 89970 |
rs753440118 | snp | C/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188161 | TTGCTTTTAAATTTC[C/T]CTTGCACAGTGGTTC | 89970 |
rs753448527 | snp | C/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187176 | CTCTCTGTAGATCGA[C/T]CAGGTGTCCCAGACA | 89970 |
rs753464259 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225850 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG | 89970 |
rs753512296 | snp | C/T | 1.80448e-05 | 0.00300368 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227481 | TCCATTATAAATTTA[C/T]CAAGTGGGTTAAGAC | 89970 |
rs753645603 | snp | C/G/T | 3.62761e-05 | 0.00425875 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235088 | TAACAGGACCCCTGT[C/G/T]GACAAAATGTATTTC | 89970 |
rs753730366 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198720 | CAGTTATTTTTAGTA[C/T]GTGATTAGTCTCCCT | 89970 |
rs753733501 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214293 | GCGTTCCAAGCCAGG[A/T]GGCCATCAAGTCAGA | 89970 |
rs753734782 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212905 | TTTTGTCTCAAAAAA[A/C]AAATGAGCCTGGGAA | 89970 |
rs753737570 | snp | A/T | 3.3006e-05 | 0.00406226 | splice-acceptor-variant | RSPRY1 | GRCh38.p7 | 16:57216105 | CTTTTGTTGTTTTTC[A/T]GAAGTTACAGTCCCA | 89970 |
rs753771549 | snp | A/G | 1.65121e-05 | 0.00287329 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216862 | TGAGCAAATCATTCT[A/G]CCCTTTCATTGTTAA | 89970 |
rs753788606 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196526 | GGGCCGGCATCCCAG[A/G]AATTCTGATTCTGGC | 89970 |
rs753837538 | in-del | -/GATGACAGTG | 1.64741e-05 | 0.00286998 | frameshift-variant, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204800 | TCCTGTATCTGCCGA[-/GATGACAGTG]GAACAGATGACAGTG | 89970 |
rs753876222 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197382 | CAGAAAGTATTTAGA[A/G]GTAACAGCTCTTGAT | 89970 |
rs753926882 | in-del | -/CAGAAG | 0.000280294 | 0.0118351 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216104 | TCTTTTGTTGTTTTT[-/CAGAAG]TTACAGTCCCACCCC | 89970 |
rs753963685 | snp | C/T | 1.6543e-05 | 0.00287597 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208011 | TCTTATTTGGAATTG[C/T]CATTTATTATTTCCT | 89970 |
rs753970698 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184975 | TATTTCAGAAGGGTG[C/T]CTTCCATTTTATGGT | 89970 |
rs753980893 | snp | C/T | 3.3083e-05 | 0.00406699 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221268 | CATTTTTTGGTTTTG[C/T]CAGGCTCGCTGTGAT | 89970 |
rs754098345 | snp | A/T | 2.4773e-05 | 0.00351936 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205018 | AGATAAGTAAGTATC[A/T]GACTCACGGTCACCT | 89970 |
rs754106796 | snp | G/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240070 | ATTGGAAGGTAGAAT[G/T]GTAAATTCATAGAAC | 89970 |
rs754211338 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192009 | ATAAGCATTGGATAT[A/G]TAGTTATTGAATGGT | 89970 |
rs754264020 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239637 | TTTTACTGCAGAAAA[C/T]TGGTGGTATTTTCAC | 89970 |
rs754282738 | snp | A/T | 3.29576e-05 | 0.00405928 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213878 | TCAAGTGTTTGTTGT[A/T]TTTGTCTAGGTCCTG | 89970 |
rs754316748 | snp | C/T | 3.3657e-05 | 0.00410212 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220861 | AGGTAGGTAATGCTT[C/T]TACAGTTGGACCCTT | 89970 |
rs754365842 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231616 | TACCAAACCCAGAAA[G/T]ACGGAACACTTTCAA | 89970 |
rs754383197 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228918 | CTGGCTAGTCTCAAA[C/T]TTCTGGGCTCAAGTG | 89970 |
rs754458342 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228075 | AGTCAGGAGTTCAAG[A/C]CCAGCCTGGCCAACA | 89970 |
rs754471522 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210712 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAGA | 89970 |
rs754498410 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221461 | AGCAGTGGCAGTTTG[A/C]TTTTTCCCCCTAGTT | 89970 |
rs754528604 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214900 | GGGCATGGTGGCATG[-/T]TGTGTGTAGTCCCAG | 89970 |
rs754545223 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214756 | AATGAGGGCCGGGCA[C/T]GGTGGCTCATGCCTA | 89970 |
rs754617043 | snp | A/G | | | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216992 | TCCTGATTATCTGAA[A/G]CGTCAAGTTGGTTTC | 89970 |
rs754634894 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198078 | GTATTGGATATCATC[C/G]AATCACCTTAAAATT | 89970 |
rs754676235 | snp | C/T | 8.23798e-05 | 0.00641741 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57209155 | CCAGCTGTTATAACA[C/T]TGTTACTAGATGAAT | 89970 |
rs754729401 | snp | A/C | 0.00016335 | 0.00903594 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227484 | ATTATAAATTTATCA[A/C]GTGGGTTAAGACATC | 89970 |
rs754756262 | snp | A/G | 3.29582e-05 | 0.00405931 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216112 | TGTTTTTCAGAAGTT[A/G]CAGTCCCACCCCACA | 89970 |
rs754875152 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224897 | TCAAGTGTTCTGTCA[A/G]GGACTTCTCAGGACA | 89970 |
rs754914806 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216865 | GCAAATCATTCTACC[A/C]TTTCATTGTTAATTC | 89970 |
rs754998355 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210550 | TCTACTAAAATACCC[C/T]GTCTCTACTAAAAAT | 89970 |
rs755015679 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211438 | AGCCAGCACGATGGC[A/G]TGCACCTGTAATCCC | 89970 |
rs755020251 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196173 | TTCATTTTGATGCTT[C/T]GTAAGATGGACCTCA | 89970 |
rs755051982 | snp | C/G | 1.65141e-05 | 0.00287346 | missense | RSPRY1 | GRCh38.p7 | 16:57221272 | TTTTGGTTTTGCCAG[C/G]CTCGCTGTGATGCCT | 89970 |
rs755088363 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193748 | ATGCATTTGATAAAA[C/T]TCAGCACGTTACTGT | 89970 |
rs755105664 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194650 | CAATAGTAATTTAGT[A/G]CCCAAAGTCTGGTTT | 89970 |
rs755216085 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219395 | GTAGTTTTGATTTGG[A/G]TTTCTCTGATGATCA | 89970 |
rs755216093 | snp | C/T | 3.2963e-05 | 0.00405961 | missense | RSPRY1 | GRCh38.p7 | 16:57231256 | AATACCCACCATCTA[C/T]GAAATTTAGCACTTT | 89970 |
rs755232444 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240085 | TGTAAATTCATAGAA[C/T]TTCTTTTATAATGGT | 89970 |
rs755251786 | in-del | -/TCT | 0.000165393 | 0.00909226 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209055 | GACTCCATCATATAA[-/TCT]TCTTGATTTGCTCTT | 89970 |
rs755252902 | snp | C/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239797 | AAGGTACCATCAAAT[C/G]AGATTTCTGTTTTTT | 89970 |
rs755291083 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199331 | AGATCTGTCTCTACT[A/G]AAAATACAAAATTAG | 89970 |
rs755344445 | snp | C/T | 0.000217214 | 0.0104192 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205025 | TAAGTATCTGACTCA[C/T]GGTCACCTCCAGTGG | 89970 |
rs755378495 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220602 | CACAAACATGGATAA[C/T]TTGACTTCTTCCTTT | 89970 |
rs755394988 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239083 | ACACATTGAAACTTA[C/T]AGCCATGGCCAGATT | 89970 |
rs755432070 | snp | G/T | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205618 | GAATAACAGTGAAAT[G/T]AAAGGGCATCCAAGT | 89970 |
rs755475021 | snp | A/C/T | 0.000115341 | 0.00759339 | synonymous-codon, missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204890 | ACAAGGAGCCAACCA[A/C/T]GGGACCCTGTTCGGC | 89970 |
rs755509657 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229575 | AGTGAGCTAGGATTG[-/T]ACCACTGCACTCCAG | 89970 |
rs755531929 | snp | C/T | 1.68527e-05 | 0.00290277 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220862 | GGTAGGTAATGCTTC[C/T]ACAGTTGGACCCTTT | 89970 |
rs755551404 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237269 | CTGCCTCAGCCTCCC[A/G]AGTAGCTTGGATTAC | 89970 |
rs755582563 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202080 | TAATCCCAATACTTG[A/G]GAGGCCAAGATGAGA | 89970 |
rs755653113 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218244 | TACAATGAGTAATTA[A/C]CACATCAGAGTAAAT | 89970 |
rs755671197 | snp | A/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240376 | AAAATATATATATAT[A/T]TAAATATATATGTAG | 89970 |
rs755784401 | in-del | -/TATATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202881 | TATTACATATGATTA[-/TATATA]TATATATATATATAT | 89970 |
rs755860396 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224967 | TTATGCCACAATGCC[C/T]ACATTTTAGTGGTTT | 89970 |
rs755872502 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225804 | GAAGAAACTGCCAGG[C/T]GCGGTGGCTCACGCC | 89970 |
rs755876965 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233719 | TTCCCTGGCCATAAC[C/T]GTAGAGTATCCTTGA | 89970 |
rs755887850 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | RSPRY1 | GRCh38.p7 | 16:57221306 | CTTTTGAAAGTGTGC[A/G]TTGCACCTTTTGTGT | 89970 |
rs755890430 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232478 | TGCCTGACAGAGATT[C/T]TGAACTTTAAATTCC | 89970 |
rs755899418 | snp | A/C | 1.64822e-05 | 0.00287068 | missense | RSPRY1 | GRCh38.p7 | 16:57231235 | ATTTTGGAGCAAAAC[A/C]ATTCAAATACCCACC | 89970 |
rs755912847 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210664 | GTTGCAGTGAGCTGA[G/T]ATTGTGCTACTGCAC | 89970 |
rs756004639 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211661 | TTGGTTATCCTTTAC[A/G]TAGAACAAAAGCATC | 89970 |
rs756041587 | snp | G/T | 0.0966627 | 0.197453 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216098 | TTTTTATCTTTTGTT[G/T]TTTTTCAGAAGTTAC | 89970 |
rs756056698 | snp | A/T | 1.83337e-05 | 0.00302762 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235077 | TGCATCACTGCTAAC[A/T]GGACCCCTGTTGACA | 89970 |
rs756094594 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57213937 | ACTGGAATACTTGCT[A/G]CAGTGTCTGGTAAGT | 89970 |
rs756102076 | snp | A/C | 3.3036e-05 | 0.0040641 | missense | RSPRY1 | GRCh38.p7 | 16:57220833 | TACCTGAAGATCTCA[A/C]CTCATGGCTTAGAGG | 89970 |
rs756171037 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204758 | CACTTCCTAGGGACT[A/G]GAGGTGCCGCTACTA | 89970 |
rs756178504 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196401 | CCCCCTAGTTCAGTC[A/G]GTGTGTCCTTCCTGC | 89970 |
rs756224512 | snp | C/T | 3.39368e-05 | 0.00411913 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220684 | ACTAGCTTCTTCTTT[C/T]CTCCACAGCAGCCTG | 89970 |
rs756305853 | in-del | -/G | 4.95225e-05 | 0.00497582 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216095 | TTTTTTTTATCTTTT[-/G]TTGTTTTTCAGAAGT | 89970 |
rs756311407 | snp | C/G | 3.33717e-05 | 0.0040847 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238849 | CTTTTGAAGCATTAA[C/G]TTGACTGACTTTTCT | 89970 |
rs756345428 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205832 | GATTATCATGAGATA[A/G]TGTACATAAGGCATT | 89970 |
rs756400927 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237734 | ATTTATTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 89970 |
rs756488062 | in-del | -/AAA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228273 | GTGAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 89970 |
rs756491674 | snp | C/T | 1.66821e-05 | 0.00288804 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212952 | TATGGGTCAAACCCA[C/T]TTGTACTTTTTTGTT | 89970 |
rs756615420 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191932 | TAAGTTTGTCCCTAA[C/T]CCCAGCTCCCTTTGT | 89970 |
rs756616961 | snp | C/G | | | missense | RSPRY1 | GRCh38.p7 | 16:57227427 | ATGCCAGAAGTAAGC[C/G]TCACATACACCCATG | 89970 |
rs756724219 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | RSPRY1 | GRCh38.p7 | 16:57213020 | TTAAATGGAGAAGTA[A/G]CTTGCCAGGACTCAA | 89970 |
rs756740517 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | RSPRY1 | GRCh38.p7 | 16:57213915 | TAGGTTTACTTAGCC[C/T]AGGAATACTGGAATA | 89970 |
rs756898986 | in-del | -/AC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236760 | TCATAAAAAGAAAAA[-/AC]TATTTTTTTATGAAT | 89970 |
rs756902111 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225861 | AGGCGGGCAGATCAC[C/G]TGAGGTCTAGAGTTC | 89970 |
rs756979100 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230631 | ACTTAATACAGTGCC[A/G]TTGAAACACTTGAGA | 89970 |
rs757019571 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192017 | TGGATATATAGTTAT[C/T]GAATGGTGTTGTCTC | 89970 |
rs757052336 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195317 | AGGAGTTCAAGACCA[G/T]CCTGGTGAACATGGT | 89970 |
rs757061549 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204820 | CAGTGGAACAGATGA[C/T]AGTGTTGACACCCAA | 89970 |
rs757171440 | in-del | -/T | 0.000149513 | 0.00864489 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208045 | GTTTAATGCCTTGAA[-/T]TTTTTTTTCCAGTGA | 89970 |
rs757240879 | snp | A/G | 1.68323e-05 | 0.00290101 | missense | RSPRY1 | GRCh38.p7 | 16:57230809 | CAAGTCTTTTCATCT[A/G]CTGTGTAAGTAGCTC | 89970 |
rs757242337 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190219 | AAAAAAATACAAAAA[-/T]TTAGCCCAGCGTGGT | 89970 |
rs757259994 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197495 | GTTTTCACAGATGGT[C/T]CTTTTTATTTAAAAA | 89970 |
rs757318122 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185002 | TGGTGTCCCTGTGGA[C/T]ACATGAATACACCAA | 89970 |
rs757321093 | snp | C/T | 1.65551e-05 | 0.00287702 | missense | RSPRY1 | GRCh38.p7 | 16:57238964 | ATCAGACAGATTTCT[C/T]ATATTTCATGACACA | 89970 |
rs757356949 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237108 | GGAGGTGGAGGTTGC[A/G]GTGAGCAGAGATCGT | 89970 |
rs757370472 | snp | C/T | 3.47427e-05 | 0.00416775 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235262 | GGCAAAGTTTCATAC[C/T]GTTCTTAAATTGCTA | 89970 |
rs757371696 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | RSPRY1 | GRCh38.p7 | 16:57216934 | CTATTTCTGAATCCA[A/G]TATTAGTGACCGGCT | 89970 |
rs757414627 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209730 | CCAGGCTGGCGTGCA[A/G]TAGAGCAATCACAGC | 89970 |
rs757466195 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191062 | ATTATAGTTTCCAGG[C/T]GTAATTTCATAGGTC | 89970 |
rs757468338 | snp | G/T | 1.64811e-05 | 0.00287059 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217071 | ATTAAAATGTCCGTT[G/T]CCATTTCCAGACTCA | 89970 |
rs757512744 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207263 | TGAAATGACCATACT[A/G]ATTCCCATATCACAA | 89970 |
rs757514631 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223059 | AAACACTCTTCCCTG[A/G]TCCAAGCATTAGGTG | 89970 |
rs757517174 | snp | A/G | 1.65124e-05 | 0.00287331 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208043 | AGGTTTAATGCCTTG[A/G]ATTTTTTTTTCCAGT | 89970 |
rs757545989 | snp | A/G | 3.29522e-05 | 0.00405894 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204728 | CTGTTGTTGACTCTC[A/G]AAGAGCACATAGCCC | 89970 |
rs757638926 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192025 | TAGTTATTGAATGGT[A/G]TTGTCTCAGTTTTTC | 89970 |
rs757733654 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228650 | TTGTTGTTATACTTA[A/G]TACCTTGAACAGCTT | 89970 |
rs757760861 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217181 | TATATTCTAGCAGAA[A/G]AGTATCCTAGAGACC | 89970 |
rs757803911 | snp | C/T | 6.59228e-05 | 0.00574083 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57209172 | GTTACTAGATGAATG[C/T]CCATTGCCCACTAAA | 89970 |
rs757822893 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | RSPRY1 | GRCh38.p7 | 16:57209092 | GAAGGATGGTTGGAT[A/G]TTGTCCAGTCTTTAA | 89970 |
rs757856710 | in-del | -/CAC | 1.64737e-05 | 0.00286994 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216193 | TATAGTGACTTCTTG[-/CAC]CACTAATGATCTTCT | 89970 |
rs757856753 | snp | C/T | 1.91985e-05 | 0.0030982 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227500 | GTGGGTTAAGACATC[C/T]GGTTATTATGAGGCA | 89970 |
rs757885968 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196698 | AATTACTTCAGTACG[A/G]GGTAGTTCTGTAAAA | 89970 |
rs757898792 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190511 | TCAAAAGAATTATTT[A/G]GGGATAATAAACTAT | 89970 |
rs757935764 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230406 | ACCACATGATTTTTT[G/T]ATCTTACCATATTTC | 89970 |
rs758087510 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213186 | TTTGATCAAACTGCT[A/G]TACCAGAAAGAAATC | 89970 |
rs758119207 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196712 | GGGGTAGTTCTGTAA[A/C]AGATAAATTCTTTAC | 89970 |
rs758159141 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217493 | TTCCTGATTTTTCTC[-/T]TTTCCTCCTCCAAGG | 89970 |
rs758162228 | snp | C/T | 1.67959e-05 | 0.00289787 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204635 | GTTATGAAAACAGTA[C/T]TTGGAAAACTGAAAA | 89970 |
rs758212771 | snp | C/G | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185242 | AACAAACAGGTCTCC[C/G]CCTTTCCTCTGTGTG | 89970 |
rs758237416 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222355 | TACCTCAGCCTCCTG[A/G]ATAGCTGAGACTACA | 89970 |
rs758269200 | snp | A/G | 4.95029e-05 | 0.00497484 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216877 | ACCCTTTCATTGTTA[A/G]TTCAAGGATTATGTC | 89970 |
rs758306925 | snp | C/G/T | 4.94363e-05 | 0.00497153 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204705 | CGAGCAGAAGCCTTG[C/G/T]CCAGGGTCTGTTGTT | 89970 |
rs758399727 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186305 | GACTGAGGGAGGGCT[A/G]GGGCGGTACGAAGCG | 89970 |
rs758420349 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223391 | AGTTCTGTTCAGGTA[A/G]CCTACAGAACAGTTT | 89970 |
rs758436672 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235655 | CAGCAAGAGAAGCAA[A/G]TAAGATGGTCCCCAG | 89970 |
rs758517360 | snp | C/T | 1.74199e-05 | 0.00295121 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235107 | AAAATGTATTTCAAA[C/T]TGCTTTTTCTACTCA | 89970 |
rs758646037 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209389 | CCTCTTTGAGACAAG[A/G]GTCTCACTCTGTTGC | 89970 |
rs758648949 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192394 | CCCTGTACTGCAACC[A/G]TCATAAGCATTTACC | 89970 |
rs758734939 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193695 | AATATGTTTCTAGAT[A/C]ATGTTCTCTATCTTG | 89970 |
rs758749068 | snp | A/G | 1.70064e-05 | 0.00291597 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235243 | GGTAAGAGGATTTAT[A/G]TTAGGCAAAGTTTCA | 89970 |
rs758777088 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217530 | GGGACAAAAACTACT[A/G]TAGGTTGAGTTTCTC | 89970 |
rs758901790 | snp | A/T | 0.000148776 | 0.00862357 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208026 | TCATTTATTATTTCC[A/T]CAGGTTTAATGCCTT | 89970 |
rs758910539 | snp | G/T | 1.64781e-05 | 0.00287033 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220769 | GACCTATGAGAAAGT[G/T]AACTTGAGTAGCATT | 89970 |
rs758949007 | snp | C/T | 0.000272401 | 0.0116673 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205032 | CTGACTCACGGTCAC[C/T]TCCAGTGGAATGAAA | 89970 |
rs758952599 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240316 | TGCTGGATTTTTTTC[C/T]GTGTCTTTAGTCTTC | 89970 |
rs758953343 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204261 | AAAAATCAATGATAA[C/T]TCCTCTGGTCTATAA | 89970 |
rs759027197 | snp | G/T | 1.64808e-05 | 0.00287057 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204696 | TGTTCTTAGCGAGCA[G/T]AAGCCTTGGCCAGGG | 89970 |
rs759138187 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204796 | TAATTCCTGTATCTG[C/T]CGAGATGACAGTGGA | 89970 |
rs759158701 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217973 | TGGAAGCATAAATCT[A/G]GCAGTGCTGCCTTTC | 89970 |
rs759178699 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214220 | GATTGGCTCTTTTGC[A/G]TGTTCCTTGAGTTTG | 89970 |
rs759258068 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238053 | TATGTATAATAGCAG[A/C]CAGTTAGAACATATA | 89970 |
rs759262015 | snp | A/C | 1.65537e-05 | 0.0028769 | missense | RSPRY1 | GRCh38.p7 | 16:57230755 | AATGAAAAGCAAATG[A/C]TCTTCTTTTTAAATG | 89970 |
rs759277764 | in-del | -/GGCAGAGACGCTCCTCACTTCCTAGATGGGATGGCGGCCG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201408 | GACGATGGGCGGCCT[lengthTooLong]GGCAGAGACGCTCCT | 89970 |
rs759348278 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236518 | AGAGTCAATCCCCAG[A/G]GGAGACTGAAAATCT | 89970 |
rs759360298 | snp | A/G | 1.67837e-05 | 0.00289682 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235233 | TGTGGACACAGGTAA[A/G]AGGATTTATATTAGG | 89970 |
rs759369078 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219781 | ATTTTAGTAGCTTCA[C/T]AGTTTGAGGTCTTAG | 89970 |
rs759370489 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198828 | GTATGGAAAGGCTGT[A/G]GGGTATTAGAGCAGC | 89970 |
rs759401136 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203892 | GCCTTGCTTACATAA[C/G]AGAAACACTTTGCAA | 89970 |
rs759501519 | snp | C/T | 1.65767e-05 | 0.00287891 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238868 | ACTGACTTTTCTGTG[C/T]TTCTCCCCAGTGACC | 89970 |
rs759501557 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234772 | AGAAAGCCTCTATGC[-/T]TTGTGAGCAGACTCT | 89970 |
rs759509867 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | RSPRY1 | GRCh38.p7 | 16:57217035 | AGCTTAGACAATCTC[C/T]GTAAGTGGGAGTTGT | 89970 |
rs759523597 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225459 | GTCACTTTGGAGAGC[A/G]TTCCTCCAAATTCAG | 89970 |
rs759574979 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187733 | GGAGTGCTGGGAGCC[A/G]TATTGTACTGAAAGC | 89970 |
rs759613507 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226408 | TATAGGCAGAGCAGT[A/G]GCGTGGGCTGCTCAA | 89970 |
rs759623367 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223466 | CTCTCCAAGGGTGTA[C/G]TCTGATTTATCTAAA | 89970 |
rs759628758 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199854 | TTTTTTTTTTTTTTC[-/C]CACTCCAAACCTCAG | 89970 |
rs759701434 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212733 | GATTCTCCTGCCTAA[C/G]CCTCCTGAGTAGCTG | 89970 |
rs759790956 | snp | C/T | 3.30989e-05 | 0.00406797 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208012 | CTTATTTGGAATTGT[C/T]ATTTATTATTTCCTC | 89970 |
rs759791177 | snp | A/G | 6.62855e-05 | 0.00575659 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57227380 | TGAATACTCCTGTGC[A/G]TATGATGGCTGCCGG | 89970 |
rs759793278 | snp | A/G | | | missense | RSPRY1 | GRCh38.p7 | 16:57213920 | TTACTTAGCCCAGGA[A/G]TACTGGAATACTTGC | 89970 |
rs759885878 | snp | G/T | 1.73348e-05 | 0.00294399 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216058 | TAACTTGCCACCTCT[G/T]CAGGGGAATGATTTT | 89970 |
rs759890833 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184566 | CTAATGGTGAACACG[C/T]TGAAAATGCTTAATT | 89970 |
rs760032277 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233084 | ATGTATATTCAGTGA[C/T]ACTTTATATTCATTG | 89970 |
rs760070519 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211004 | GCCTGGTTAAAAAAA[G/T]AAGTATTTGTATCTC | 89970 |
rs760083259 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206980 | CTGCTTCTGACTATT[A/G]CAGAGTATTCCCTTG | 89970 |
rs760124257 | snp | A/T | 1.6476e-05 | 0.00287014 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216212 | TAATGATCTTCTGTA[A/T]TGGTTGTTAAAAATT | 89970 |
rs760135167 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222865 | ACAGATCTAGGTCTG[A/G]CACTGAATGTTACAA | 89970 |
rs760152166 | in-del | -/CTAC | 1.66205e-05 | 0.00288271 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204651 | TTGGAAAACTGAAAA[-/CTAC]CTAAATGATCGTCTT | 89970 |
rs760197405 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219971 | TGAGTTCACTGTAGA[C/T]GTATGGATTTCTGGA | 89970 |
rs760236034 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234724 | ATAAACCCCTTGAAA[C/T]TGTATAAAAACTTGT | 89970 |
rs760287087 | snp | C/T | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205423 | TACAGGCAACTTCTC[C/T]TGGCAACATAAGGAC | 89970 |
rs760322218 | snp | A/T | 0.000368868 | 0.0135756 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207691 | TTTCTCTGAGGTAAG[A/T]ATGAAGGTGATGTTG | 89970 |
rs760353400 | snp | A/G | 4.94181e-05 | 0.00497057 | missense | RSPRY1 | GRCh38.p7 | 16:57216994 | CTGATTATCTGAAAC[A/G]TCAAGTTGGTTTCTG | 89970 |
rs760370321 | in-del | -/TTTTTTTTTTTTTTTTTTTG | 1.72469e-05 | 0.00293652 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216076 | GGGAATGATTTTTTT[-/TTTTTTTTTTTTTTTTTTTG]TTTTTTTTTTTATCT | 89970 |
rs760479296 | in-del | -/TATG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213398 | TCAGCATAACAAAGA[-/TATG]TATGTGTGTATACAA | 89970 |
rs760506576 | in-del | -/TTTG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188516 | TGTGTTTTTGGTTTT[-/TTTG]TTTGTTTGTTTTTTG | 89970 |
rs760506902 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206248 | ATCTCTGCAAAAAAA[A/G]TTTAAAAATTATCCA | 89970 |
rs760509703 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230500 | AGATTGGCTTGTCAT[A/T]ATTTAATTGGCAGTA | 89970 |
rs760556491 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234447 | TCTTCCCCTACTGGA[A/G]CATAAGCTCTCCAAA | 89970 |
rs760678073 | in-del | -/ATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208397 | TATATATATATATAT[-/ATA]ATATTTTTTTTTTTT | 89970 |
rs760737747 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214075 | TTGTAAATTTTATTT[A/G]CAGGTGTTTCCCGAG | 89970 |
rs760778619 | snp | C/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239892 | TAATAGTCTCAAAAA[C/G]TCTAGAGGACAGTCT | 89970 |
rs760871055 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193493 | GGTGTTCTGCAGGCT[-/T]TTTTTTTTTTTTCTT | 89970 |
rs760941433 | snp | G/T | 2.01056e-05 | 0.00317055 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205000 | AGTAATACGGACTCT[G/T]GTAGATAAGTAAGTA | 89970 |
rs760987815 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231471 | ATAAATTTCTAAGAT[C/G]GCAGAAGAAATATAC | 89970 |
rs760991596 | snp | A/G | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184780 | TTCCTTTCTTATATC[A/G]TGAAGCACTTCCCCA | 89970 |
rs761022009 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198341 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 89970 |
rs761038789 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208832 | TTTAATGTGAGAGCA[C/T]AAGACCATAGCTTAA | 89970 |
rs761145733 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188706 | TTTTTAGTAGAGACG[A/T]GGTTTCTCCGTGTTG | 89970 |
rs761147081 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219573 | TTAATCCTTTGTCGA[A/G]TGGATAGTTTGCAAA | 89970 |
rs761171906 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187993 | TCCTCCCCCTTTTGC[-/AT]ATATATATATGCATG | 89970 |
rs761234558 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230269 | CGCCCGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 89970 |
rs761248057 | snp | A/G | 1.65078e-05 | 0.00287291 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213995 | CATCTAGAAGTGGGC[A/G]TCATCTAGAACTGTG | 89970 |
rs761264618 | snp | A/G | 3.33178e-05 | 0.00408139 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231356 | TCTCCAGACTTTCAC[A/G]TGAATCTTATGAGAA | 89970 |
rs761267937 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233266 | TCAAATACATACAGA[A/G]GAAAAAAATAATAGT | 89970 |
rs761334880 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234541 | GCACACAGTAAGCCC[A/G]TAAGTGAACTGAATA | 89970 |
rs761362728 | in-del | -/T | 3.7784e-05 | 0.00434633 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230863 | ATGCACGGAATGCCC[-/T]TTTCTCTAGGAAAAA | 89970 |
rs761444090 | snp | A/G | 1.64737e-05 | 0.00286994 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216193 | GTATAGTGACTTCTT[A/G]CACTAATGATCTTCT | 89970 |
rs761459970 | snp | A/G | 1.66399e-05 | 0.00288438 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221249 | CCCTCATAGTTGATT[A/G]ACACATTTTTTGGTT | 89970 |
rs761649427 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191484 | CCTGGCACCAATACA[A/G]GCTTCTCACATGTCA | 89970 |
rs761762220 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214321 | AGATTCCCAGTATAT[A/G]TAAATCTCTACTCCT | 89970 |
rs761771771 | in-del | -/TTTTTTTTTTTTTTTTTTG | 1.70382e-05 | 0.0029187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216080 | ATGATTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTG]TTTTTTTATCTTTTG | 89970 |
rs761820744 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238572 | ATTCTGGGATAAATG[A/G]CTAGCTTTCTGGGGA | 89970 |
rs761873595 | snp | A/C | 1.85149e-05 | 0.00304255 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204991 | CACACTGGCAGTAAT[A/C]CGGACTCTTGTAGAT | 89970 |
rs761957647 | snp | C/T | | | upstream-variant-2KB, stop-gained, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57186070 | TTCCGGCGACGTAAC[C/T]CAATCCGCGGAGCTC | 89970 |
rs762031852 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203433 | ACTAGCCAGATGTTG[C/T]GTAGAGACTACACAC | 89970 |
rs762047539 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186799 | AGGTGAGAGGCAGCT[A/G]TCTATCTCCTGGGGT | 89970 |
rs762089461 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204380 | GTATTGGAAACCTAT[-/A]AAAAATAACCAAAGA | 89970 |
rs762090806 | snp | C/T | 3.29766e-05 | 0.00406045 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220814 | TAGCAATGATGTCAG[C/T]GAGTACCTGAAGATC | 89970 |
rs762173268 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193545 | TCACCCAGGCTTGAG[G/T]GTAGTGGGATGATCT | 89970 |
rs762199329 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219109 | TATTGTGAATAATGC[C/T]GCAATAAACATGCGA | 89970 |
rs762215040 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230135 | CCTGCTTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 89970 |
rs762270272 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208303 | AATGCATATTATACC[-/T]TTTTTTTTTTTTTTT | 89970 |
rs762284159 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219252 | CTGTTCTCCATAGTG[C/G]CCATACTAATTTGCA | 89970 |
rs762300339 | snp | C/T | 1.64999e-05 | 0.00287222 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204931 | GGGCCGAGGACCTCA[C/T]GAGCCAAGGAGAAAG | 89970 |
rs762391723 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231617 | ACCAAACCCAGAAAG[A/T]CGGAACACTTTCAAA | 89970 |
rs762398806 | snp | C/T | 1.85235e-05 | 0.00304326 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230860 | TAGATGCACGGAATG[C/T]CCTTTTCTCTAGGAA | 89970 |
rs762417800 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194227 | AAAAACTGAATGGAT[G/T]AATGATGGATAAGAG | 89970 |
rs762451948 | snp | C/T | 1.67891e-05 | 0.00289729 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57230715 | TTATCCTCTAGGAGA[C/T]ACAGTAGGATTTCTG | 89970 |
rs762534521 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191741 | CATAAATGTGTTACA[A/G]TGCAAAGATAGATTC | 89970 |
rs762559815 | snp | G/T | 1.68581e-05 | 0.00290324 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231131 | TATTTTGATTTTTAT[G/T]AATTCTATTGGCCTC | 89970 |
rs762621402 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193001 | GATTACAGGTGTGAG[A/C]CACCATGCCCTGCTC | 89970 |
rs762660880 | snp | C/T | 1.66048e-05 | 0.00288134 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231345 | TGCCCAGGCTATCTC[C/T]AGACTTTCACATGAA | 89970 |
rs762762030 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186322 | GGCGGTACGAAGCGG[C/G]GGTGGGCTCTGCGCG | 89970 |
rs762838952 | snp | G/T | 1.64985e-05 | 0.0028721 | missense | RSPRY1 | GRCh38.p7 | 16:57238892 | AGTGACCTGTGCATG[G/T]ATTGTGCCTTGCAGC | 89970 |
rs762845600 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238419 | TTAATAGTTTGGTCC[C/T]ATTACTATATGACAA | 89970 |
rs762892499 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199427 | AACGTGGGAGGCAGA[G/T]GTTGCAGTGAGCCAA | 89970 |
rs762927397 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186868 | TGCCCGGGATAGAAA[C/G]GGTAGATGAAGGGAC | 89970 |
rs762930410 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217911 | AAAGAATAATTCTGA[A/G]AGAGTGCAATTTGGA | 89970 |
rs762933318 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204803 | TGTATCTGCCGAGAT[A/G]ACAGTGGAACAGATG | 89970 |
rs762949902 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224221 | TGCTGGAAATCCATC[C/T]TAACTATCCCTCTGT | 89970 |
rs762970360 | snp | C/T | 1.67142e-05 | 0.00289081 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221229 | TATCTTTGGTGGTCT[C/T]CAGGCCCTCATAGTT | 89970 |
rs762988041 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225437 | TATCAATAGCTATTT[C/T]AGAAGAGTCACTTTG | 89970 |
rs763006867 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203893 | CCTTGCTTACATAAC[-/AG]AAACACTTTGCAACA | 89970 |
rs763021842 | snp | C/G/T | 3.29578e-05 | 0.00405931 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220790 | GAGTAGCATTAGGGC[C/G/T]ATGCTGAATAGCAAT | 89970 |
rs763041023 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192238 | ATTTTATTTGCTTTT[A/C]TTAAGAGCAGAGAGT | 89970 |
rs763128692 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226332 | AAGAAAGAATTTGGG[A/G]CGAATCCATAGAATA | 89970 |
rs763167860 | snp | C/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187576 | TGAAAGTACAAATTA[C/T]AAGCTGCGTGAACGT | 89970 |
rs763172798 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229916 | TTCACCATGTTGGCT[C/G]TGCTGGTCTCAAACT | 89970 |
rs763190098 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225274 | CCATGTTGGCCAGGC[C/T]GGTCTCAAATGCCTG | 89970 |
rs763268554 | snp | A/G | 1.66369e-05 | 0.00288412 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209234 | CATTTGTGCTTAAGC[A/G]CAAGATAAATGACCA | 89970 |
rs763278728 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211362 | ATCACTTGAGGTCAG[A/G]AGTTCAAGACCAGCC | 89970 |
rs763396619 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204677 | ATCGTCTTTGGTTGG[A/G]CCGTGTTCTTAGCGA | 89970 |
rs763397434 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194525 | TTAAAATTTTCAGGA[A/T]GTTACACATTTTGCT | 89970 |
rs763520121 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194540 | TGTTACACATTTTGC[C/T]ATTCATGCTATTTGA | 89970 |
rs763568409 | in-del | -/TTTTTTTTTTTTTTTTG | 1.71366e-05 | 0.00292712 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216078 | GAATGATTTTTTTTT[-/TTTTTTTTTTTTTTTTG]TTTTTTTTTATCTTT | 89970 |
rs763598945 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231684 | CAGAAAAATATGACA[C/G]ATGCACACAAACTGC | 89970 |
rs763624296 | in-del | -/CA | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240346 | CCATAAATCCACACA[-/CA]CACACACACACAAAA | 89970 |
rs763629092 | in-del | -/G | 1.64743e-05 | 0.00287 | frameshift-variant, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204767 | GGGACTGGAGGTGCC[-/G]CTACTACCATGGGTA | 89970 |
rs763662233 | in-del | -/A | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239169 | CTTGCCAGCCCTGAG[-/A]AAATCCCTTTTAAGG | 89970 |
rs763668574 | snp | C/G | 1.66382e-05 | 0.00288424 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231353 | CTATCTCCAGACTTT[C/G]ACATGAATCTTATGA | 89970 |
rs763735470 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213882 | GTGTTTGTTGTATTT[A/G]TCTAGGTCCTGCAAG | 89970 |
rs763780562 | snp | G/T | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205432 | CTTCTCTTGGCAACA[G/T]AAGGACTAAGGTCAA | 89970 |
rs763813042 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189942 | GCTTTCCTTAACAAT[A/G]AAGTAATTTGTTCTA | 89970 |
rs763835513 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227139 | GGCACTGGGAAAATA[C/T]TTGTTGGTGAAGTCA | 89970 |
rs763877610 | snp | C/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188115 | GTTGTTGTGGTAGCC[C/G]TAGACTATAGATTAT | 89970 |
rs763896778 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238474 | TAAAAGCCCAGAAAT[A/T]GAACTAACTAAAAAT | 89970 |
rs763917598 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203909 | GAAACACTTTGCAAC[A/C]ACTTGTATGAATTCT | 89970 |
rs764003975 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212871 | GCCCGCCTCGGCCTC[C/T]CAAAGTGCTGGTTAT | 89970 |
rs764010744 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217059 | GAGTTGTCCTTTATT[A/G]AAATGTCCGTTTCCA | 89970 |
rs764052129 | snp | A/C | 1.66588e-05 | 0.00288602 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209235 | ATTTGTGCTTAAGCA[A/C]AAGATAAATGACCAC | 89970 |
rs764091798 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196504 | GCTTTTAAGAAAACA[C/T]AAGCTTGGGCCGGCA | 89970 |
rs764095809 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192379 | ACATTTGTTTTTCTT[-/C]CCTGTACTGCAACCG | 89970 |
rs764142099 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237028 | AAAAAATTACCCGGG[C/T]GTGGTGGTGGGCGCC | 89970 |
rs764184145 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197370 | GTGTAGTCATCTCAG[A/T]AAGTATTTAGAGGTA | 89970 |
rs764258700 | snp | A/G | 3.29826e-05 | 0.00406082 | missense | RSPRY1 | GRCh38.p7 | 16:57209077 | GATTTGCTCTTAGAT[A/G]AAGGATGGTTGGATG | 89970 |
rs764274089 | snp | G/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184805 | TCCCCACAGGGTAAG[G/T]ACATGAAGACTTCAG | 89970 |
rs764281987 | snp | A/G | 1.64969e-05 | 0.00287196 | missense | RSPRY1 | GRCh38.p7 | 16:57238935 | CATTGTGTCGTAAAG[A/G]AATAGTATCTAGAAT | 89970 |
rs764298281 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211195 | GCACTTTGGGAGACC[A/G]AGGCAGGAGGATCAG | 89970 |
rs764315110 | in-del | -/TTCAAGTGATCCTC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210175 | CCTCAACCTCTCAGG[-/TTCAAGTGATCCTC]TTGCCTCAGCTTCCC | 89970 |
rs764353106 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221435 | GTACCCTAGAGAACT[A/G]TGAAAATGGGAGCAG | 89970 |
rs764405547 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222136 | GGGAAAAGCCCCTTG[C/G]ATTATTTTGTTAATC | 89970 |
rs764489395 | in-del | -/GG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200949 | CGGGGCGGCTGGCCG[-/GG]GGGGGGGGGGGCTGA | 89970 |
rs764548990 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208898 | ACTCCTGTAACTTAA[C/G]ATGTTTTTACTCCAC | 89970 |
rs764578240 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193390 | TCAGCTGGCAAGTGT[A/C]ATCTTCATGCATTAC | 89970 |
rs764675550 | snp | A/T | 1.64803e-05 | 0.00287052 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204697 | GTTCTTAGCGAGCAG[A/T]AGCCTTGGCCAGGGT | 89970 |
rs764752072 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206762 | GTAGAGCCAGGTCTT[A/G]CCATGTTGCCCAGGC | 89970 |
rs764913637 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190296 | ATCTCTTGAGCCTGG[G/T]AGGTTGAAGATGCAG | 89970 |
rs764974884 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214453 | CTCTCATAGTTCTGG[C/T]CTGTGGTCTTGAATG | 89970 |
rs765015518 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217039 | TAGACAATCTCTGTA[A/G]GTGGGAGTTGTCCTT | 89970 |
rs765023048 | in-del | -/ATAT | 5.07327e-05 | 0.00503624 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208146 | ATTACTTTATAATGA[-/ATAT]ATAATAATGAAGAAA | 89970 |
rs765065063 | snp | A/C | 1.65053e-05 | 0.0028727 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216870 | TCATTCTACCCTTTC[A/C]TTGTTAATTCAAGGA | 89970 |
rs765068508 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197733 | TTTGTTTTTGTTTTT[A/G]TTTTCCCAAAGACAG | 89970 |
rs765129071 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236665 | AGGTAGCCCAATTCT[A/G]TTTAAACTTGGCCAA | 89970 |
rs765141220 | snp | A/G | 1.6519e-05 | 0.00287388 | missense | RSPRY1 | GRCh38.p7 | 16:57238881 | TGTTTCTCCCCAGTG[A/G]CCTGTGCATGGATTG | 89970 |
rs765203582 | in-del | -/TCCC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210028 | TCTTCTTTCTTTCTT[-/TCCC]TCCCTCCCTCCCTCC | 89970 |
rs765218951 | snp | A/G | | | missense | RSPRY1 | GRCh38.p7 | 16:57235194 | CTTTGTTGTGATGAG[A/G]TAGCAGACACACAAT | 89970 |
rs765274569 | snp | A/T | 9.92195e-05 | 0.00704272 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208019 | GGAATTGTCATTTAT[A/T]ATTTCCTCAGGTTTA | 89970 |
rs765276897 | snp | A/G | 1.65438e-05 | 0.00287605 | missense | RSPRY1 | GRCh38.p7 | 16:57227394 | CGTATGATGGCTGCC[A/G]GCAGCTGATTTGGTA | 89970 |
rs765289789 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199260 | AGCACTTTGGTAGGC[C/T]GAGGCGGGCGGATCA | 89970 |
rs765296424 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198854 | GCAGCCAGTGGAGTT[C/G]CCCTCTGCTGTGGCA | 89970 |
rs765365248 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224177 | GGTGTTTTAGGGAAA[C/T]GATCTGGCCAGCATG | 89970 |
rs765371820 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228004 | ATGGATATAAACTGA[A/C]TTTTTAGGCATGCTA | 89970 |
rs765400160 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223090 | ATTCCCTATTAGAAA[C/T]TGATAAAGTCTGATA | 89970 |
rs765542057 | snp | A/G/T | 3.45008e-05 | 0.00415324 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216061 | CTTGCCACCTCTGCA[A/G/T]GGGAATGATTTTTTT | 89970 |
rs765631494 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210171 | GTATCCTCAACCTCT[C/G]AGGTTCAAGTGATCC | 89970 |
rs765671537 | snp | G/T | 1.64999e-05 | 0.00287222 | missense | RSPRY1 | GRCh38.p7 | 16:57221276 | GGTTTTGCCAGGCTC[G/T]CTGTGATGCCTCCTC | 89970 |
rs765808665 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190584 | TATCATTGAATTTGG[G/T]TAGTTTTTTCCCTGA | 89970 |
rs765809042 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194295 | AGTAGAGTCTAGGTG[A/G]TGGGGATAAAGCAAG | 89970 |
rs765832824 | snp | G/T | 8.25648e-05 | 0.00642461 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216855 | AATTTGCTGAGCAAA[G/T]CATTCTACCCTTTCA | 89970 |
rs765885203 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57217004 | GAAACGTCAAGTTGG[C/T]TTCTGTGCCCAGTGG | 89970 |
rs765896878 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191761 | AAGATAGATTCTCTA[A/G]TCCCCTTTTGCTATT | 89970 |
rs766104382 | in-del | -/CTG | 1.65015e-05 | 0.00287237 | cds-indel | RSPRY1 | GRCh38.p7 | 16:57235168 | CAGTATCCGAGAAAA[-/CTG]CTGCTGTTCCCTTTG | 89970 |
rs766165814 | snp | C/G | 1.64991e-05 | 0.00287215 | missense | RSPRY1 | GRCh38.p7 | 16:57235177 | GAGAAAACTGCTGTT[C/G]CCTTTGTTGTGATGA | 89970 |
rs766185327 | snp | A/G | 1.8332e-05 | 0.00302748 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235079 | CATCACTGCTAACAG[A/G]ACCCCTGTTGACAAA | 89970 |
rs766202723 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186317 | GCTGGGGCGGTACGA[A/G]GCGGGGGTGGGCTCT | 89970 |
rs766213267 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195883 | AAAAATTAGCTGAGC[A/G]TGGTGGCACGCACCT | 89970 |
rs766215401 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216803 | CTAATCTAGTCTCCA[A/G]TTCTTTAATTGCCTC | 89970 |
rs766216046 | snp | G/T | 1.65425e-05 | 0.00287593 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208009 | ATTCTTATTTGGAAT[G/T]GTCATTTATTATTTC | 89970 |
rs766276961 | snp | A/C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233738 | GAGTATCCTTGACAC[A/C/G]TTACTTTCTGCTATT | 89970 |
rs766405025 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225312 | GTGATCTGCCCCCCA[A/C]AGTGCTGAAATTACA | 89970 |
rs766406017 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186888 | GATGAAGGGACGCTT[A/T]AGGAGGGTTCTTTTT | 89970 |
rs766426622 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224240 | CTATCCCTCTGTTTG[G/T]GGTCACTTGCACCAT | 89970 |
rs766428851 | snp | C/T | 1.65589e-05 | 0.00287736 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221264 | GACACATTTTTTGGT[C/T]TTGCCAGGCTCGCTG | 89970 |
rs766446217 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230612 | TGCATAGCTAAAGAT[G/T]CAGACTTAATACAGT | 89970 |
rs766466070 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240058 | TTCTCCCAGGAAATT[A/G]GAAGGTAGAATTGTA | 89970 |
rs766514265 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210422 | ATAGAAGCATTTAAG[A/G]CTGGGCGCGGTGGTT | 89970 |
rs766517538 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | RSPRY1 | GRCh38.p7 | 16:57221368 | GTGGTCACTTCTGGC[A/G]TCATGCAGATTGGCT | 89970 |
rs766579390 | snp | C/G | 2.42792e-05 | 0.00348411 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205017 | TAGATAAGTAAGTAT[C/G]TGACTCACGGTCACC | 89970 |
rs766608341 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199840 | ATCAGTGAAATTTCT[-/T]TTTTTTTTTTTTCCC | 89970 |
rs766667700 | snp | C/T | | | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57238945 | TAAAGAAATAGTATC[C/T]AGAATCAGACAGATT | 89970 |
rs766776485 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194606 | ACATCCTCTAACACT[A/G]TTTTGGAATGATAAG | 89970 |
rs766826496 | snp | A/T | 6.59283e-05 | 0.00574106 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213868 | TTTAATTATATCAAG[A/T]GTTTGTTGTATTTGT | 89970 |
rs766846205 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230331 | TTGCCTTTTTTTAAA[G/T]AAAGGCATATTTTGG | 89970 |
rs766860743 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220288 | GTCTTCCAATCCATG[A/G]CCATGGTATATCTTT | 89970 |
rs766870188 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231583 | GGTAACAGATAACCT[C/T]ATTGTTATTTAAAAT | 89970 |
rs766875613 | snp | G/T | 3.3269e-05 | 0.00407841 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212959 | CAAACCCACTTGTAC[G/T]TTTTTGTTTTAGGAT | 89970 |
rs766914727 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192709 | TTTTTCCAGAGACTC[-/T]TTTTTTTTTTTTTTT | 89970 |
rs767046574 | snp | A/G | 1.66687e-05 | 0.00288688 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231358 | TCCAGACTTTCACAT[A/G]AATCTTATGAGAAAT | 89970 |
rs767156090 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233456 | AGGTCATTGCAACCT[C/T]CATCTCCCAGGCTCA | 89970 |
rs767181968 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204092 | AAAGAAAGGAGTTAA[C/T]TCATTTTTTTAAAGA | 89970 |
rs767224634 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216206 | TTGCACTAATGATCT[A/T]CTGTATTGGTTGTTA | 89970 |
rs767353869 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203914 | ACTTTGCAACAACTT[G/T]TATGAATTCTGTCAG | 89970 |
rs767368814 | snp | A/C | 1.6617e-05 | 0.00288239 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221254 | ATAGTTGATTGACAC[A/C]TTTTTTGGTTTTGCC | 89970 |
rs767384245 | snp | G/T | 1.64942e-05 | 0.00287173 | missense | RSPRY1 | GRCh38.p7 | 16:57231193 | TTGCTGCAGCTAGTT[G/T]CATGTCATATCAACA | 89970 |
rs767390490 | snp | A/C | 3.73748e-05 | 0.00432273 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204992 | ACACTGGCAGTAATA[A/C]GGACTCTTGTAGATA | 89970 |
rs767440011 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205332 | ATGGTTTCATGAAGG[C/T]TCACTGTTAATGGTA | 89970 |
rs767481595 | in-del | -/GTTA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199564 | TGAAGCTTTTAAGAG[-/GTTA]GTTATCTCTGGGAAA | 89970 |
rs767525165 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226508 | AGGGACAGGCAATTC[C/T]TGGAACCAAGGGTTC | 89970 |
rs767527760 | snp | C/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187789 | ATATTAAGATCTAAA[C/T]CCATGGTTTCAAACC | 89970 |
rs767569426 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220820 | TGATGTCAGCGAGTA[C/T]CTGAAGATCTCACCT | 89970 |
rs767608357 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196264 | GGATATAACCATTCT[A/G]ATGGCTTTTTAGGCT | 89970 |
rs767667675 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195507 | ATGAGAGTGGAACTC[C/T]GTCTGAAAAAATAAA | 89970 |
rs767751415 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | RSPRY1 | GRCh38.p7 | 16:57209141 | AAGATCCACTGGGAC[C/T]AGCTGTTATAACATT | 89970 |
rs767757232 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192790 | GGTTTACTGCAGCCT[C/T]GACCTCCCCAGCTCA | 89970 |
rs767895104 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222870 | TCTAGGTCTGGCACT[A/G]AATGTTACAAATGTG | 89970 |
rs767933362 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230162 | ATTACAGGTGCCCAC[C/G]ACCACACCCAGCTAA | 89970 |
rs767933409 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184589 | GCTTAATTTAGCTGC[C/T]ATAAAGGCATAATTA | 89970 |
rs767960219 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221878 | ATTTTTCTCAATATT[G/T]AGTTATTTATCTTTT | 89970 |
rs768052064 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207037 | ACATTTTCATCTGGT[A/G]ATGGTCACTTAGGTT | 89970 |
rs768094233 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228763 | CAGTGGTGTGATCAT[A/T]GCTCATACAGCCTTG | 89970 |
rs768139975 | snp | C/T | 1.67363e-05 | 0.00289272 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212943 | TGTGTAGTATATGGG[C/T]CAAACCCACTTGTAC | 89970 |
rs768163670 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216459 | ATGGTGGCTCTTGCC[C/T]ATAATCCCAGCACTT | 89970 |
rs768241699 | snp | C/G | 0.000371609 | 0.0136259 | intron-variant, missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57207595 | GTGGTATTTCCAGAA[C/G]AAAACTTCAAAATGA | 89970 |
rs768277585 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221660 | GCTAATTTTTCACCT[A/G]GAGGCTGGATGTGTC | 89970 |
rs768288468 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196866 | GTTAGGCACTGTGCC[A/T]TGCGTATTACATGCA | 89970 |
rs768294786 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | RSPRY1 | GRCh38.p7 | 16:57221330 | TTTGTGTGGATGCCG[A/G]GGTATGGTACTATGA | 89970 |
rs768296692 | snp | A/G | 1.65222e-05 | 0.00287417 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204945 | ATGAGCCAAGGAGAA[A/G]GAAACAAAATGTGGA | 89970 |
rs768315659 | in-del | -/TTATC | 1.64727e-05 | 0.00286986 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227478 | CCCTCCATTATAAAT[-/TTATC]AAGTGGGTTAAGACA | 89970 |
rs768344573 | snp | C/G | 1.6495e-05 | 0.0028718 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213974 | TCAAAACTATTTATT[C/G]TTAGTCATCTAGAAG | 89970 |
rs768365942 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222690 | TATTCTACAACAGTT[A/G]TTTTCTTTGTATTCA | 89970 |
rs768413055 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222829 | AAAACTTGTCTCTCC[G/T]GATTTGGCAGCAAAC | 89970 |
rs768437855 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194258 | ATGGATAGCGATAAA[-/G]CAAGTTTAGTAAAAT | 89970 |
rs768506978 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239496 | ACAGTCAGTACTACA[A/G]GCAAAACAGAGAACC | 89970 |
rs768513963 | snp | G/T | 0.00036914 | 0.0135806 | intron-variant, splice-donor-variant | RSPRY1 | GRCh38.p7 | 16:57207687 | GGCATTTCTCTGAGG[G/T]AAGTATGAAGGTGAT | 89970 |
rs768599608 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191328 | TACTTAGGTATGCCT[A/G]AGGGCTACTTATTAA | 89970 |
rs768643108 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216309 | TCATCTGGATAGACA[A/C]GTTAAAGCCAATGAA | 89970 |
rs768716140 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229577 | TGAGCTAGGATTGTA[C/G]CACTGCACTCCAGCC | 89970 |
rs768876504 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231115 | TTCTATCTATTAACT[C/G]TATTTTGATTTTTAT | 89970 |
rs768928342 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203021 | TCTAAAATAATGGAA[A/G]TAGGCTGGGCACAGT | 89970 |
rs768981891 | snp | G/T | 1.65765e-05 | 0.00287888 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213104 | AAACTAGCAGGTAAC[G/T]TTGGGACACTCCACA | 89970 |
rs769017186 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237772 | GCTTGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 89970 |
rs769024641 | snp | A/C | 1.6473e-05 | 0.00286988 | missense | RSPRY1 | GRCh38.p7 | 16:57216987 | AATGATCCTGATTAT[A/C]TGAAACGTCAAGTTG | 89970 |
rs769102266 | snp | G/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187281 | AGTCCAAATTAGGCA[G/T]TTGTCTCTCCTGCTG | 89970 |
rs769154116 | snp | G/T | 1.75576e-05 | 0.00296285 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220884 | GGACCCTTTGGGGGA[G/T]GAGAGGGTAATTATT | 89970 |
rs769263528 | in-del | -/ATTTT | 1.66096e-05 | 0.00288176 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231154 | TTGGCCTCTGTACTC[-/ATTTT]ATTTGTAGATCTGGA | 89970 |
rs769264945 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225205 | AACTGGGATTATAGG[G/T]GTGCGCCACCACACC | 89970 |
rs769299375 | snp | C/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239419 | CTCACTGGTCAGAGA[C/T]ACCGGTGTGTCAAGC | 89970 |
rs769320905 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222828 | TAAAACTTGTCTCTC[C/T]TGATTTGGCAGCAAA | 89970 |
rs769355243 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210906 | GCCTATAGTCCCAGC[C/T]GCTCAGGAGGCTGAG | 89970 |
rs769366108 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220773 | TATGAGAAAGTGAAC[C/T]TGAGTAGCATTAGGG | 89970 |
rs769373349 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222161 | TAATCTAAATAATAG[-/C]CCCCCCCCTCCAATA | 89970 |
rs769428815 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185691 | GGCTTCGGCTACTCC[A/G]GACAAGGAGCGGGTG | 89970 |
rs769459201 | in-del | -/CGC | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186402 | GTCACAAAGGAGTCG[-/CGC]CGCCGCCGCCGCCGC | 89970 |
rs769500647 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209826 | ACCATAGGTGCATGA[C/T]CCCATGTCTGGCTAA | 89970 |
rs769589350 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192879 | AAGCCGCCACTCTGG[C/G]TAATTTGTGTATTTT | 89970 |
rs769679314 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193820 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 89970 |
rs769690382 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217757 | GATTAAGAGTGATCA[A/G]CCTGTATACTTCTGT | 89970 |
rs769770614 | snp | A/G | 3.30153e-05 | 0.00406283 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204672 | AAATGATCGTCTTTG[A/G]TTGGGCCGTGTTCTT | 89970 |
rs769780501 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203501 | TGTCAGCCTGTTTTG[A/T]TTGTTTGTTTGTTTT | 89970 |
rs769920896 | snp | A/G | 1.7991e-05 | 0.00299919 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239023 | ACTCAATTCCAGCCA[A/G]TGTTGAAAAGAAAAA | 89970 |
rs769934953 | in-del | -/A | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239041 | TTGAAAAGAAAAAGA[-/A]AAAAAAAACTCTCTA | 89970 |
rs769935656 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219606 | GTTTCTCCCATTCTG[C/T]GGGATGTCTCTTTAC | 89970 |
rs770023638 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205161 | GCTCCGCTGATGGCA[A/G]AGTAAATGATAAGAT | 89970 |
rs770114153 | snp | A/T | 1.76042e-05 | 0.00296678 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235271 | TCATACTGTTCTTAA[A/T]TTGCTAGTTCCATGG | 89970 |
rs770119650 | snp | C/G | 1.81477e-05 | 0.00301223 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230684 | GTACACATCATTATC[C/G]TAACAGTGTTTCTCT | 89970 |
rs770133404 | in-del | -/CTC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218082 | TTACGAGCATCTCTA[-/CTC]CTTGACTAGGGTAGC | 89970 |
rs770145934 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194020 | GTGGTAAACTGGGAT[C/T]ACACCAGTGCACTCC | 89970 |
rs770162480 | snp | A/C | 3.29462e-05 | 0.00405857 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216186 | CAAGTAGGTATAGTG[A/C]CTTCTTGCACTAATG | 89970 |
rs770165585 | snp | A/G | 4.9764e-05 | 0.00498794 | missense | RSPRY1 | GRCh38.p7 | 16:57235137 | AGGCACAGGCGTCTT[A/G]CTCTGTTGAAGCAAG | 89970 |
rs770253220 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234119 | TATTTCCTACCCTCT[C/T]CCGTTTTCTCATGCT | 89970 |
rs770264013 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216953 | TAGTGACCGGCTTGT[C/T]ACATTGGAGTCCTGG | 89970 |
rs770286447 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213759 | CTAGTACTATTTTCT[A/G]CCTCAGAGCAGGAGG | 89970 |
rs770325048 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228513 | TTTAAAGGATTATTC[A/G]AGTAATATGTTTATT | 89970 |
rs770374497 | snp | G/T | 1.68647e-05 | 0.0029038 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239007 | TCGTGGACTTTTTTC[G/T]ACTCAATTCCAGCCA | 89970 |
rs770405592 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223961 | AAGCCATGTAGTCTC[C/T]AGCTGCTAGAGATTT | 89970 |
rs770448631 | snp | C/T | 3.31697e-05 | 0.00407231 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238866 | TGACTGACTTTTCTG[C/T]GTTTCTCCCCAGTGA | 89970 |
rs770481963 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195864 | CGTCTTTACTAAAAA[G/T]ACAAAAAATTAGCTG | 89970 |
rs770552382 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220760 | TAGACAGCTGACCTA[C/T]GAGAAAGTGAACTTG | 89970 |
rs770568048 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197319 | CTTTGTTCATTTATG[A/T]GCCCTGTCTGTGGCT | 89970 |
rs770597485 | snp | A/C/G | 3.40984e-05 | 0.00412895 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208155 | TAATGAATATATAAT[A/C/G]ATGAAGAAAAGTAGC | 89970 |
rs770602617 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207334 | GGGGCTTTTTTTTTT[C/T]CCACACTAAAACAGA | 89970 |
rs770670498 | snp | C/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187229 | TTATTGCCCGAGTGG[C/G]GTGGGGAGAGTCTAT | 89970 |
rs770735693 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229459 | CCATCTCTATAAAAA[A/C]ATTTTAAAAATTTGC | 89970 |
rs770784671 | in-del | -/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197668 | AATTTGGAAAAAAAC[-/TT]AATTTTTGTCTTCTT | 89970 |
rs770955562 | snp | C/T | 1.65531e-05 | 0.00287686 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209203 | GTAAGTTAATACTTA[C/T]CTTTTATGAAACTAT | 89970 |
rs770967981 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219695 | CCATTTTTGCTTTGG[C/T]GCCTGTGCTTTTGGG | 89970 |
rs771054277 | snp | C/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205219 | TTTGTCTGGAAATGT[C/G]TAAATGTTTCTGTAG | 89970 |
rs771056349 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221078 | CTGCAAACAATTCTT[C/T]GATTCTGTATGTTGC | 89970 |
rs771147908 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | RSPRY1 | GRCh38.p7 | 16:57216163 | CGCACTGGAAAAGTT[G/T]GCACAGACAAGTAGG | 89970 |
rs771147930 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205977 | TTGATAATCGCATTT[A/G]TAGAAACCCAGTTTC | 89970 |
rs771214632 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232940 | GTGGCCACCTTAGTG[C/G]CAACCTCCTTCTTGC | 89970 |
rs771215958 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227713 | TCAAGATTAGTATGA[A/G]TTCTATTTTCCTCTT | 89970 |
rs771262416 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238012 | TGACTTACAAAATAC[A/G]CAAAAATCAGTAGCT | 89970 |
rs771310691 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197120 | CCTTGGAAAGTGGGC[C/T]ACGTAAAGCTTTTTT | 89970 |
rs771324075 | snp | C/T | 3.30639e-05 | 0.00406581 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204664 | AACTACCTAAATGAT[C/T]GTCTTTGGTTGGGCC | 89970 |
rs771455560 | in-del | -/TGTC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196932 | TAAGAACTGTTACTA[-/TGTC]TGTTTTTTAACATGT | 89970 |
rs771549387 | snp | A/G | 1.65471e-05 | 0.00287633 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57235145 | GCGTCTTGCTCTGTT[A/G]AAGCAAGTCAGTATC | 89970 |
rs771588548 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195437 | GAATCGCCTGAACCG[A/G]GGAGATGGAGGTTGC | 89970 |
rs771616958 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228226 | TGCAATGAGCCGAGG[C/T]TGCGCCACTGCACTC | 89970 |
rs771619618 | snp | C/T | 3.3432e-05 | 0.00408838 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208136 | TTTTGTTTTCATTAC[C/T]TTATAATGAATATAT | 89970 |
rs771628012 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194098 | CACATTTCAGTGTAT[G/T]TAAATTCGACTCCTA | 89970 |
rs771628498 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213998 | CTAGAAGTGGGCATC[A/G]TCTAGAACTGTGCAT | 89970 |
rs771668073 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193756 | GATAAAACTCAGCAC[A/G]TTACTGTGCTTAAGA | 89970 |
rs771735773 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | RSPRY1 | GRCh38.p7 | 16:57221363 | TAACAGTGGTCACTT[C/T]TGGCGTCATGCAGAT | 89970 |
rs771780442 | snp | A/G | 3.33868e-05 | 0.00408562 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238844 | TTGACCTTTTGAAGC[A/G]TTAACTTGACTGACT | 89970 |
rs771806942 | in-del | -/TTTG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188519 | TTTTTGGTTTTTTTG[-/TTTG]TTTGTTTGTTTTTTG | 89970 |
rs771924373 | snp | A/G | | | missense | RSPRY1 | GRCh38.p7 | 16:57221342 | CCGGGGTATGGTACT[A/G]TGAAGTAACAGTGGT | 89970 |
rs771990988 | in-del | -/CCTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210049 | CTCCCTCCCTCCCTT[-/CCTT]CCTCCCTTCCTCCCT | 89970 |
rs772110173 | snp | G/T | 1.78835e-05 | 0.00299022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227325 | TTGCTAATCTTCTGG[G/T]CCTTGTCTCTCTCCA | 89970 |
rs772135010 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198068 | AAATCTGCGTGTATT[-/G]GATATCATCCAATCA | 89970 |
rs772196800 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189857 | TGGCCTCCCAAGGTG[C/T]TAGGATTACAGGTGT | 89970 |
rs772241594 | snp | A/G | 3.29989e-05 | 0.00406182 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213985 | TATTCTTAGTCATCT[A/G]GAAGTGGGCATCATC | 89970 |
rs772260362 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214004 | GTGGGCATCATCTAG[A/G]ACTGTGCATTTTCTC | 89970 |
rs772268849 | in-del | -/CTGACCCCCCGCCTCCCTCGCGGAAGGGGCGGCTGGCCAGGCGGGGGA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200661 | TGGCCGGGCGGGGGG[lengthTooLong]CTGACCCCCCCACCT | 89970 |
rs772296693 | snp | C/T | 4.94482e-05 | 0.00497209 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57231281 | CACTTTTAATGACTA[C/T]GCCTTCCTAACAGCT | 89970 |
rs772346500 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215636 | TTCAGGGAACAGCTT[A/C]AAAACTGAGCCATTA | 89970 |
rs772359618 | in-del | -/AGGGAAACG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224170 | AATAGCCGGTGTTTT[-/AGGGAAACG]ATCTGGCCAGCATGC | 89970 |
rs772383157 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204892 | AAGGAGCCAACCACG[A/G]GACCCTGTTCGGCCA | 89970 |
rs772415821 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185835 | CCTACCGGCGCGCGG[C/G]AGGCGAGACGACCTC | 89970 |
rs772562549 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222856 | AAACACACTACAGAT[C/T]TAGGTCTGGCACTGA | 89970 |
rs772578727 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236129 | TGAGCATATTTGGAG[A/G]GTTTAGTTATCAGGG | 89970 |
rs772658371 | snp | A/G | 1.65132e-05 | 0.00287339 | missense | RSPRY1 | GRCh38.p7 | 16:57235158 | TTGAAGCAAGTCAGT[A/G]TCCGAGAAAACTGCT | 89970 |
rs772775649 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230862 | GATGCACGGAATGCC[C/T]TTTTCTCTAGGAAAA | 89970 |
rs772849903 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234695 | GACTTGCAGGGAGTC[C/T]AAAATGAACTGTTAT | 89970 |
rs772856496 | snp | A/G | 3.29516e-05 | 0.00405891 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216211 | CTAATGATCTTCTGT[A/G]TTGGTTGTTAAAAAT | 89970 |
rs772881632 | snp | C/T | 1.7336e-05 | 0.00294409 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227334 | TTCTGGGCCTTGTCT[C/T]TCTCCAGGAAGGCTA | 89970 |
rs772924493 | snp | G/T | 5.00697e-05 | 0.00500323 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238845 | TGACCTTTTGAAGCA[G/T]TAACTTGACTGACTT | 89970 |
rs772968595 | snp | A/T | 3.36848e-05 | 0.00410381 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208142 | TTTCATTACTTTATA[A/T]TGAATATATAATAAT | 89970 |
rs772985394 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188441 | TTCGTCGTACTTGTT[-/A]AGAGATGGTTTTCCA | 89970 |
rs773112439 | snp | G/T | 1.64741e-05 | 0.00286998 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57221364 | AACAGTGGTCACTTC[G/T]GGCGTCATGCAGATT | 89970 |
rs773184793 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230235 | AGGCTGGTCTTCAAA[C/T]TCCTGACCTCAGGTG | 89970 |
rs773203322 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216730 | GTGACTAAAAAAAAG[G/T]AAAACAAAATAGTCA | 89970 |
rs773204670 | in-del | -/CAAAATGTATTT | 1.81007e-05 | 0.00300833 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235091 | CAGGACCCCTGTTGA[-/CAAAATGTATTT]CAAATTGCTTTTTCT | 89970 |
rs773291940 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217848 | ACCCCCACTGTTACC[C/G]CAATATTGTGGGGAG | 89970 |
rs773301214 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203507 | CCTGTTTTGTTTGTT[C/T]GTTTGTTTTTTTACT | 89970 |
rs773322896 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225266 | GGGTTTCGCCATGTT[G/T]GCCAGGCTGGTCTCA | 89970 |
rs773339399 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232812 | TTGGTACCCAAAGTT[C/T]GTCTTGTCTTGAATA | 89970 |
rs773471644 | snp | A/G | 1.65004e-05 | 0.00287227 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213989 | CTTAGTCATCTAGAA[A/G]TGGGCATCATCTAGA | 89970 |
rs773476661 | in-del | -/CTG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233746 | TTGACACCTTACTTT[-/CTG]CTATTTCCACATTCA | 89970 |
rs773602163 | snp | C/G | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204897 | GCCAACCACGGGACC[C/G]TGTTCGGCCACCAAG | 89970 |
rs773624131 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219554 | TCCTTATATATTCTG[G/T]TTATTAATCCTTTGT | 89970 |
rs773676089 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211103 | CTAAGCAATTTCCTC[A/G]TAACAAAAGTTTTAA | 89970 |
rs773694744 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209899 | AGGCTGGTCTTGAAA[C/T]TCCTGGGCTCAAGCA | 89970 |
rs773764357 | in-del | -/AT | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240364 | ACACACACACAAAAA[-/AT]ATATATATATATAAA | 89970 |
rs773809073 | snp | A/C | 1.64822e-05 | 0.00287068 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213866 | ATTTTAATTATATCA[A/C]GTGTTTGTTGTATTT | 89970 |
rs773811067 | snp | A/C | 1.64841e-05 | 0.00287085 | missense | RSPRY1 | GRCh38.p7 | 16:57231283 | CTTTTAATGACTACG[A/C]CTTCCTAACAGCTGA | 89970 |
rs773827008 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233171 | TGGGATTTTATAAAT[C/T]GTTCTGTGTTGTATA | 89970 |
rs773853661 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195881 | CAAAAAATTAGCTGA[A/G]CGTGGTGGCACGCAC | 89970 |
rs773864146 | snp | A/T | 1.92558e-05 | 0.00310282 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230864 | TGCACGGAATGCCCT[A/T]TTCTCTAGGAAAAAA | 89970 |
rs773918146 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187680 | GTAGTATGTAGAGGT[-/A]AGGGGTGGGATTAAT | 89970 |
rs773953397 | snp | G/T | 1.65616e-05 | 0.00287759 | missense | RSPRY1 | GRCh38.p7 | 16:57235141 | ACAGGCGTCTTGCTC[G/T]GTTGAAGCAAGTCAG | 89970 |
rs773959298 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210737 | AAAAGAAGCATTTAG[A/G]TTGGGCGCAGTGGCT | 89970 |
rs774045976 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194028 | CTGGGATCACACCAG[C/T]GCACTCCATCCTGGG | 89970 |
rs774109690 | snp | G/T | 3.29457e-05 | 0.00405854 | missense | RSPRY1 | GRCh38.p7 | 16:57221332 | TGTGTGGATGCCGGG[G/T]TATGGTACTATGAAG | 89970 |
rs774110667 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188705 | ATTTTTAGTAGAGAC[G/T]AGGTTTCTCCGTGTT | 89970 |
rs774204509 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239572 | ATTTCAGTGATTCCA[A/G]AGAACATTCTAGGTT | 89970 |
rs774241360 | in-del | -/CGC | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186405 | ACAAAGGAGTCGCGC[-/CGC]CGCCGCCGCCGCCCC | 89970 |
rs774254365 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217965 | CTAGGGAATGGAAGC[A/C]TAAATCTAGCAGTGC | 89970 |
rs774291802 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229870 | GCCATTAACACCCGG[C/G]TAATTTTTGTATATT | 89970 |
rs774344437 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219769 | CCCCAATGTTTTATT[G/T]TAGTAGCTTCATAGT | 89970 |
rs774383239 | snp | C/T | 1.85088e-05 | 0.00304204 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204990 | ACACACTGGCAGTAA[C/T]ACGGACTCTTGTAGA | 89970 |
rs774434412 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205246 | GTAGCAGAAAACACG[A/G]TAAAGCTATGATCTT | 89970 |
rs774445236 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212710 | ACCTCTACCTCCCAG[A/G]TTCAAGTGATTCTCC | 89970 |
rs774477762 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226387 | GAAACAGAAGAATGG[C/T]TACTCTATAGGCAGA | 89970 |
rs774522246 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206098 | CTGGAGCATTTGTTA[A/G]TCTTCGAGAAGAATA | 89970 |
rs774539531 | snp | A/C | 1.66651e-05 | 0.00288657 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209239 | GTGCTTAAGCACAAG[A/C]TAAATGACCACAAAG | 89970 |
rs774733900 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213807 | GCATGAAAGAGTTCT[A/G]CCAAAACAATTTGAT | 89970 |
rs774739184 | snp | G/T | 1.64966e-05 | 0.00287194 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204680 | GTCTTTGGTTGGGCC[G/T]TGTTCTTAGCGAGCA | 89970 |
rs774742765 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230080 | CAATGGCATGATGTC[A/G]TCTCACTGCAACCTC | 89970 |
rs774790738 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185481 | ATCCGAGTGAGTAAC[C/T]TGGACCTGTTCCAAG | 89970 |
rs774884186 | in-del | -/TTT | 0.0174566 | 0.0917799 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216070 | TCTGCAGGGGAATGA[-/TTT]TTTTTTTTTTTTTTT | 89970 |
rs774922147 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187759 | AAAGCTTCAAGGTTC[A/G]CAGCTTCTTAGGTCA | 89970 |
rs775044863 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTG | 1.82964e-05 | 0.00302455 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216073 | CAGGGGAATGATTTT[-/TTTTTTTTTTTTTTTTTTTTTTG]TTTTTTTTTTTTTTA | 89970 |
rs775058971 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204903 | CACGGGACCCTGTTC[A/G]GCCACCAAGGAGGGG | 89970 |
rs775075962 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236398 | AGAGTTGGAAGAGGA[-/C]CATTAAAAGAATTAT | 89970 |
rs775085121 | in-del | -/A | 1.66599e-05 | 0.00288611 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204647 | GTACTTGGAAAACTG[-/A]AAACTACCTAAATGA | 89970 |
rs775105854 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195442 | GCCTGAACCGGGGAG[A/T]TGGAGGTTGCAGTGA | 89970 |
rs775175053 | snp | G/T | 1.69209e-05 | 0.00290864 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231122 | TATTAACTCTATTTT[G/T]ATTTTTATTAATTCT | 89970 |
rs775188711 | snp | A/G | 1.78398e-05 | 0.00298657 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220889 | CTTTGGGGGATGAGA[A/G]GGTAATTATTTTAAT | 89970 |
rs775200128 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206167 | CAACACTTTTGAGAG[G/T]CTGAGGTAGAAAGAT | 89970 |
rs775214144 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186320 | GGGGCGGTACGAAGC[C/G]GGGGTGGGCTCTGCG | 89970 |
rs775220416 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219970 | ATGAGTTCACTGTAG[A/T]TGTATGGATTTCTGG | 89970 |
rs775238426 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239423 | CTGGTCAGAGACACC[A/G]GTGTGTCAAGCATGG | 89970 |
rs775330382 | in-del | -/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186899 | GCTTTAGGAGGGTTC[-/T]TTTTGTGGAGTTTAC | 89970 |
rs775406616 | in-del | -/AATT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206409 | AGACCCTGTCTCAAA[-/AATT]AATTAATCAAAAAAA | 89970 |
rs775526478 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220784 | GAACTTGAGTAGCAT[C/T]AGGGCCATGCTGAAT | 89970 |
rs775529010 | in-del | -/CA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194357 | GGTGGGTATATAGTT[-/CA]CAGTTTACAGTGAAC | 89970 |
rs775579081 | snp | C/T | 0.00015417 | 0.00877856 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230704 | AGTGTTTCTCTTTAT[C/T]CTCTAGGAGATACAG | 89970 |
rs775657119 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191219 | CCCTTAATGCAGTGA[C/T]TCTCAAGATGTGGTT | 89970 |
rs775672663 | in-del | -/CCTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210046 | CTCCCTCCCTCCCTC[-/CCTT]CCTCCCTTCCTCCCT | 89970 |
rs775690600 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197235 | AAAAAAAAAATACCA[C/T]GAATGACAGCCATTT | 89970 |
rs775692677 | snp | C/T | 1.6522e-05 | 0.00287414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209061 | ATCATATAATCTTCT[C/T]GATTTGCTCTTAGAT | 89970 |
rs775694612 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215693 | TGCAACTTGTTAGTG[A/C]TAAGTGGTTCTTTTT | 89970 |
rs775768863 | snp | C/G | 1.64732e-05 | 0.0028699 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216190 | TAGGTATAGTGACTT[C/G]TTGCACTAATGATCT | 89970 |
rs775784604 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199128 | GTAGTTACATATATA[C/T]TGATATAGAAGGTTG | 89970 |
rs775852702 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186721 | GTTCCCTCTTTCGGG[A/G]GTCCTCACCAGAAGA | 89970 |
rs775856934 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218016 | TGATTGATCTTCAAA[A/T]GGCAGTGCAGCAGGA | 89970 |
rs775873234 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223962 | AGCCATGTAGTCTCC[A/G]GCTGCTAGAGATTTC | 89970 |
rs775921703 | snp | A/C/T | 3.29464e-05 | 0.00405861 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216956 | TGACCGGCTTGTCAC[A/C/T]TTGGAGTCCTGGGCT | 89970 |
rs775935590 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229173 | TCTCTGGCAAGGGGG[A/G]TATAGAATTTCAAAG | 89970 |
rs776005308 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234454 | CTACTGGAGCATAAG[C/T]TCTCCAAAGGCAGGG | 89970 |
rs776059388 | snp | C/G | 3.29457e-05 | 0.00405854 | missense | RSPRY1 | GRCh38.p7 | 16:57217009 | GTCAAGTTGGTTTCT[C/G]TGCCCAGTGGAGCTT | 89970 |
rs776060322 | in-del | -/TTTTTTTTTTTTTTTTTG | 1.71202e-05 | 0.00292572 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216079 | AATGATTTTTTTTTT[-/TTTTTTTTTTTTTTTTTG]TTTTTTTTATCTTTT | 89970 |
rs776142324 | in-del | -/GTAGTACACATC | 1.8519e-05 | 0.00304289 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230665 | TAGCAAAGAATCCTG[-/GTAGTACACATC]GTAGTACACATCATT | 89970 |
rs776152764 | snp | C/G | 1.70566e-05 | 0.00292027 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239011 | GGACTTTTTTCTACT[C/G]AATTCCAGCCAATGT | 89970 |
rs776160703 | in-del | -/TA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202745 | AGCCATTGCTGTCTT[-/TA]AATAGTGAAAACGTC | 89970 |
rs776214514 | snp | C/T | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204774 | GAGGTGCCGCTACTA[C/T]CATGGGTAATTCCTG | 89970 |
rs776230118 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196900 | TTTCATTTAATCCCC[A/G]CAGTGGTACTGTGAG | 89970 |
rs776273997 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222806 | TTCCAGGGAGGAAGC[C/T]TCGATATAAAACTTG | 89970 |
rs776283920 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216087 | TTTTTTTTTTTTTTT[A/T]ATCTTTTGTTGTTTT | 89970 |
rs776320137 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184285 | GAAGCAATATATGCA[C/T]ATAAAATGGCTGAGA | 89970 |
rs776346576 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57220766 | GCTGACCTATGAGAA[A/G]GTGAACTTGAGTAGC | 89970 |
rs776354737 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206425 | ATTAATTAATCAAAA[A/G]AAATTTTTTAAATCC | 89970 |
rs776357788 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237947 | GTGACACATAGGAAG[C/T]ATTTCAAGAGATGTT | 89970 |
rs776375423 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229489 | CCAGGGGTGGTGGCA[C/T]GTGCCTGTAGTCCTA | 89970 |
rs776405694 | snp | A/C | 1.65605e-05 | 0.0028775 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209204 | TAAGTTAATACTTAT[A/C]TTTTATGAAACTATC | 89970 |
rs776469496 | snp | A/G | 1.65817e-05 | 0.00287933 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238867 | GACTGACTTTTCTGT[A/G]TTTCTCCCCAGTGAC | 89970 |
rs776513414 | in-del | -/TTTGTTTT | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239592 | ATTCTAGGTTTTTTG[-/TTTGTTTT]TTTGTTTTTTTGTTT | 89970 |
rs776560230 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235252 | ATTTATATTAGGCAA[A/C]GTTTCATACTGTTCT | 89970 |
rs776602936 | in-del | -/TAT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234582 | CTTCCCTTGCCCATA[-/TAT]TATTAGGGCTGTACC | 89970 |
rs776626439 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217669 | AAAATCTGAAATCCT[C/T]CATTGAGCATTTCCT | 89970 |
rs776832655 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203055 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 89970 |
rs776847428 | snp | C/G | 1.6492e-05 | 0.00287154 | missense | RSPRY1 | GRCh38.p7 | 16:57221413 | AGCAAATTCCTCAAT[C/G]ATGTGAGTACCCTAG | 89970 |
rs776869344 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228275 | GAGACTCCATCTCAA[-/A]AAAAAAAAAAAAAAA | 89970 |
rs776913384 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191448 | AATACTTTTTTCGCC[C/G]AGGAAGTCTGTCCTG | 89970 |
rs776952520 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202579 | TCTGCTGGTTTAGAA[C/T]GTGTTCTTTTAAAAA | 89970 |
rs776965854 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234085 | TGTCCTCTCCCTTCC[C/G]TATGTTACTTTTCTG | 89970 |
rs777005902 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205973 | ACATTTGATAATCGC[A/G]TTTATAGAAACCCAG | 89970 |
rs777055993 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233016 | GGCATTAAGTATGAA[C/G]TTACTTGAGACCATT | 89970 |
rs777147113 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216172 | AAAGTTTGCACAGAC[A/G]AGTAGGTATAGTGAC | 89970 |
rs777185113 | snp | A/G | 1.66007e-05 | 0.00288098 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57230781 | AAATGGCAACCAGCT[A/G]CCTCCTGAAAAGCAA | 89970 |
rs777195594 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225210 | GGATTATAGGTGTGC[A/G]CCACCACACCTGGAT | 89970 |
rs777195811 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210013 | TTAATTGCTTTTTTT[C/T]CTTCTTTCTTTCTTT | 89970 |
rs777198350 | snp | C/G | 1.66048e-05 | 0.00288134 | missense | RSPRY1 | GRCh38.p7 | 16:57235134 | CTCAGGCACAGGCGT[C/G]TTGCTCTGTTGAAGC | 89970 |
rs777272730 | snp | G/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187174 | CTCTCTCTGTAGATC[G/T]ACCAGGTGTCCCAGA | 89970 |
rs777293450 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225003 | TTTTTTACTTACTGA[C/G]TTGTTCAGCGTTTGA | 89970 |
rs777336301 | snp | A/G | 3.35847e-05 | 0.00409771 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238997 | TGAAGAGGCATCGTG[A/G]ACTTTTTTCTACTCA | 89970 |
rs777443745 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229328 | AAAATTGGGCCAGAC[A/G]TGGTGGCTCATACTT | 89970 |
rs777450749 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193832 | GCACTTTGGGAGGCC[A/G]AGGTGGACAGATCAT | 89970 |
rs777453390 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186459 | TAGAGAAAGTCAGTG[C/T]CACAGCCCGACCGCG | 89970 |
rs777571071 | in-del | -/CA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200058 | GACCCTGCGGCCTTC[-/CA]CAGTGTTTGTGTCCC | 89970 |
rs777580520 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193836 | TTTGGGAGGCCGAGG[C/T]GGACAGATCATTTGA | 89970 |
rs777607247 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185277 | GACAGTCACAAGGAC[C/T]ACCAACTCTCAAGCA | 89970 |
rs777698896 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217804 | CCATGGTTAATACTA[C/T]GCTAAAGCATAACTG | 89970 |
rs777711728 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235738 | CGTCCTGGCCAGTCA[A/G]TGTGTGCCGATTGTT | 89970 |
rs777714316 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227502 | GGGTTAAGACATCTG[A/G]TTATTATGAGGCATT | 89970 |
rs777821909 | in-del | -/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185096 | ATCACCAGGCTCGCA[-/T]CTGGCTTCTTGGGTC | 89970 |
rs777901589 | snp | A/C | 1.72644e-05 | 0.00293801 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235257 | TATTAGGCAAAGTTT[A/C]ATACTGTTCTTAAAT | 89970 |
rs777941531 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207257 | AGTACCTGAAATGAC[C/T]ATACTAATTCCCATA | 89970 |
rs777991006 | snp | C/T | 4.94181e-05 | 0.00497057 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216148 | GCTTTTTGCACTTAT[C/T]GCACTGGAAAAGTTT | 89970 |
rs777995265 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234003 | AAAAGATGCCAGTGC[A/G]TGGCTTCTTATTCAC | 89970 |
rs778001315 | in-del | -/TTTGT | 2.25894e-05 | 0.00336068 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216095 | TTTTTTTATCTTTTG[-/TTTGT]TTGTTTTTCAGAAGT | 89970 |
rs778025670 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190901 | AGGAAAAGTTATCTT[A/G]TAAATAGTGGTGGCC | 89970 |
rs778045102 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220988 | TTCAGGGGGAAGTCT[C/G]AAAGAGCTGCTTATG | 89970 |
rs778045152 | snp | C/G | 1.67022e-05 | 0.00288978 | missense | RSPRY1 | GRCh38.p7 | 16:57235125 | CTTTTTCTACTCAGG[C/G]ACAGGCGTCTTGCTC | 89970 |
rs778072861 | snp | C/G | 4.9561e-05 | 0.00497775 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208037 | TTCCTCAGGTTTAAT[C/G]CCTTGAATTTTTTTT | 89970 |
rs778079907 | snp | G/T | 1.64895e-05 | 0.00287132 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216886 | TTGTTAATTCAAGGA[G/T]TATGTCTTTCCAAAC | 89970 |
rs778140769 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189286 | CAGGCATGAGCTACT[C/G]TGCCTGGCCCTCAGT | 89970 |
rs778141263 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237922 | TTCACCAGCTAGCAT[A/C]TTTTTAATGGTGACA | 89970 |
rs778144224 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213600 | GGGCATAGCTCAGCT[A/G]CTTACATCACGTAAT | 89970 |
rs778185780 | snp | C/T | 3.14866e-05 | 0.00396766 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205034 | GACTCACGGTCACCT[C/T]CAGTGGAATGAAAAG | 89970 |
rs778238803 | snp | C/G | 1.64827e-05 | 0.00287073 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57221289 | TCGCTGTGATGCCTC[C/G]TCTTTTGAAAGTGTG | 89970 |
rs778277150 | snp | A/G | 3.65143e-05 | 0.00427268 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227487 | ATAAATTTATCAAGT[A/G]GGTTAAGACATCTGG | 89970 |
rs778422883 | snp | C/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187222 | TCCGGGCTTATTGCC[C/G]GAGTGGGGTGGGGAG | 89970 |
rs778428085 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212019 | TTTCAATTTGCCTTC[A/T]ACTCTGTTGGGGCAG | 89970 |
rs778484186 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229115 | AATTATCATTATAGA[C/G]CATTCTGGATTTTCT | 89970 |
rs778525595 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225145 | TGCTCACTGCAACCT[C/G]TGCCTCCCAGGTTCA | 89970 |
rs778528865 | snp | A/G | 7.53665e-05 | 0.0061382 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227304 | CCCAGGTCAGAGCAG[A/G]CAGACTTGCTAATCT | 89970 |
rs778592188 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224972 | CCACAATGCCTACAT[G/T]TTAGTGGTTTTTAAG | 89970 |
rs778607950 | snp | A/C/T | 8.23708e-05 | 0.00641712 | missense, synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57216121 | GAAGTTACAGTCCCA[A/C/T]CCCACAGTCATGCTT | 89970 |
rs778629729 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193473 | AAGAAGATTGTGGTC[C/T]TTGGGGTGTTCTGCA | 89970 |
rs778644181 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57209161 | GTTATAACATTGTTA[C/T]TAGATGAATGTCCAT | 89970 |
rs778712773 | snp | A/C/G | 1.66313e-05 | 0.00288364 | | | GRCh38.p7 | 16:57213119 | TTTGGGACACTCCAC[A/C/G]GTGGAAGATCTTAAG | 89970 |
rs778808665 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222286 | TGCTTTTAGAGACAG[C/G]TCTCACTGTGTTGCT | 89970 |
rs778841803 | snp | A/C | 1.69499e-05 | 0.00291112 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204611 | AGGATGCAAATTCCT[A/C]AACTCCAGGTTATGA | 89970 |
rs778846693 | in-del | -/TCCC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210031 | CTTTCTTTCTTTCCC[-/TCCC]TCCCTCCCTCCCTCC | 89970 |
rs778914042 | in-del | -/AAAT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231409 | TTAAAAGAATATAAC[-/AAAT]AAATTTTGAAAACCT | 89970 |
rs778992079 | snp | A/G | 2.72967e-05 | 0.00369426 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205026 | AAGTATCTGACTCAC[A/G]GTCACCTCCAGTGGA | 89970 |
rs778997797 | snp | G/T | 0.000381139 | 0.0137994 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221261 | ATTGACACATTTTTT[G/T]GTTTTGCCAGGCTCG | 89970 |
rs779036355 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233883 | ACCTATATTATTTTT[A/G]TCTTGCCCTCTACCT | 89970 |
rs779071903 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217107 | TTCATAGGCTCACTG[G/T]TCTTCCTTTTGCAAT | 89970 |
rs779126297 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232571 | AGCCTGCCTTTTCCT[C/T]GGATGAAGCCCACAA | 89970 |
rs779133115 | snp | G/T | 3.2962e-05 | 0.00405954 | missense | RSPRY1 | GRCh38.p7 | 16:57231262 | CACCATCTATGAAAT[G/T]TAGCACTTTTAATGA | 89970 |
rs779143074 | snp | G/T | 1.64939e-05 | 0.0028717 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213975 | CAAAACTATTTATTC[G/T]TAGTCATCTAGAAGT | 89970 |
rs779175516 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207394 | GAGTTCTTAAGCAGT[C/T]AGAATTGTTTAATGG | 89970 |
rs779193157 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215585 | GAGTTCACTTGTTGC[C/T]TTCTCCTGTCTACCA | 89970 |
rs779214982 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184494 | TAACAACATATTCTA[C/T]AGTAAAGAGTGAAAC | 89970 |
rs779222576 | snp | A/G | 7.25992e-05 | 0.00602448 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235089 | AACAGGACCCCTGTT[A/G]ACAAAATGTATTTCA | 89970 |
rs779283118 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198560 | TATTCCTAAATACTT[C/T]TATGTGTTGGCATTA | 89970 |
rs779357184 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192044 | TCTCAGTTTTTCAAA[A/C]TGGTAAATATTTTGG | 89970 |
rs779394944 | in-del | -/TTTATTTATT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237698 | TTTTATTTTTATTTA[-/TTTATTTATT]TTTATTTATTTATTT | 89970 |
rs779508194 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237827 | AGTGATTTCTCCTGC[C/G]TCAGCCTCCCAAGTA | 89970 |
rs779561479 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196727 | AAGATAAATTCTTTA[A/C]TTTTCTTAGTGCTTT | 89970 |
rs779609526 | in-del | -/T | 1.64795e-05 | 0.00287045 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216225 | ATTGGTTGTTAAAAA[-/T]TTTTATTTTTCTTAG | 89970 |
rs779663695 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207347 | TTTCCACACTAAAAC[-/AG]AGACCCACAATATGT | 89970 |
rs779665389 | snp | A/C | | | missense | RSPRY1 | GRCh38.p7 | 16:57227367 | GCATTGGGGATGATG[A/C]ATACTCCTGTGCGTA | 89970 |
rs779706237 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | RSPRY1 | GRCh38.p7 | 16:57221323 | TGCACCTTTTGTGTG[A/G]ATGCCGGGGTATGGT | 89970 |
rs779756171 | snp | A/C | 1.64811e-05 | 0.00287059 | missense | RSPRY1 | GRCh38.p7 | 16:57231246 | AAACCATTCAAATAC[A/C]CACCATCTATGAAAT | 89970 |
rs779843327 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214569 | TACCCACTGATACGT[A/G]CTTAAAACACTTACC | 89970 |
rs779854441 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223395 | CTGTTCAGGTAACCT[A/G]CAGAACAGTTTGTCT | 89970 |
rs779867095 | snp | A/T | 3.30994e-05 | 0.004068 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57213097 | GGCCGAGAAACTAGC[A/T]GGTAACTTTGGGACA | 89970 |
rs779903964 | snp | C/T | 8.3158e-05 | 0.00644764 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216104 | TCTTTTGTTGTTTTT[C/T]AGAAGTTACAGTCCC | 89970 |
rs779923322 | snp | C/T | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185309 | GACGCTTCAACTCTC[C/T]TTGTTTCTTAAGTTT | 89970 |
rs779944221 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209467 | CTCCCGGGTCCAAGC[C/G]ATTCTCCTGCCTCAG | 89970 |
rs779949896 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222603 | AGCTTTTACTGTTAC[A/G]ATTTCCATTTCACAG | 89970 |
rs780013678 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191076 | GCGTAATTTCATAGG[C/T]CCTATGTACCTCAAA | 89970 |
rs780028458 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204762 | TCCTAGGGACTGGAG[G/T]TGCCGCTACTACCAT | 89970 |
rs780113390 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227642 | TCTGGTGGAGTTCTT[-/C]CTGTAGCAAAAACAT | 89970 |
rs780163732 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204872 | GCAGTACCCACTGCT[A/G]ACACAAGGAGCCAAC | 89970 |
rs780274135 | snp | C/T | 1.74769e-05 | 0.00295603 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230841 | TCTCAGTCAAAAATT[C/T]GAGTAGATGCACGGA | 89970 |
rs780311984 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192413 | TAAGCATTTACCTCA[A/G]TTCTTCCTTAGTATT | 89970 |
rs780337569 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212610 | TTTATTTAACACCTG[C/G]TTATAGCTCCCCCCA | 89970 |
rs780348108 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217556 | TTCTCTTTTAGGTAG[A/T]ATTTATCTGAAATGC | 89970 |
rs780369441 | snp | C/T | 1.69824e-05 | 0.00291392 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220687 | AGCTTCTTCTTTTCT[C/T]CACAGCAGCCTGCCT | 89970 |
rs780437958 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202602 | TTTAAAAAGCTATTT[C/G]CAGCTGGTCCTTGCA | 89970 |
rs780451727 | in-del | -/T | 1.66398e-05 | 0.00288437 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221462 | GCAGTGGCAGTTTGC[-/T]TTTTCCCCCTAGTTG | 89970 |
rs780526020 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204489 | TTCATTTTCCTTTTT[C/T]TCATTTTCTTTTAGA | 89970 |
rs780544436 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232563 | TTTCATCTAGCCTGC[C/G]TTTTCCTTGGATGAA | 89970 |
rs780561442 | in-del | -/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193492 | GGGTGTTCTGCAGGC[-/TT]TTTTTTTTTTTTCTT | 89970 |
rs780651206 | in-del | -/CC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199853 | CTTTTTTTTTTTTTT[-/CC]CACTCCAAACCTCAG | 89970 |
rs780657607 | snp | A/G | 0.000157424 | 0.00887058 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220882 | TTGGACCCTTTGGGG[A/G]ATGAGAGGGTAATTA | 89970 |
rs780701416 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214795 | GCATTTTGGGAGGCT[A/G]AGGTGGGCTGGTCAC | 89970 |
rs780710129 | snp | G/T | 1.64768e-05 | 0.00287021 | missense | RSPRY1 | GRCh38.p7 | 16:57213932 | GGAATACTGGAATAC[G/T]TGCTACAGTGTCTGG | 89970 |
rs780754076 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231927 | TATCAGATGAATGCC[G/T]GCTTTACTTCCTTGT | 89970 |
rs780837097 | snp | C/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239285 | CACACTGGAATCCCC[C/G]TTGTTGGGTTCATTT | 89970 |
rs780959412 | snp | G/T | 1.68758e-05 | 0.00290476 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57230811 | AGTCTTTTCATCTAC[G/T]GTGTAAGTAGCTCTT | 89970 |
rs780974212 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199839 | TATCAGTGAAATTTC[A/T]TTTTTTTTTTTTTCC | 89970 |
rs780978233 | snp | C/G | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185387 | TTGGCACAGCAACTG[C/G]TACATGGCACACAAT | 89970 |
rs781012445 | snp | A/G | 1.83266e-05 | 0.00302704 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230675 | ATCCTGGTAGTACAC[A/G]TCATTATCCTAACAG | 89970 |
rs781036254 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230645 | CATTGAAACACTTGA[A/G]ATGCTTAGCAAAGAA | 89970 |
rs781064049 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186358 | GCAGCGCCGTGGCCT[C/T]GCGTCCATCTTTGCC | 89970 |
rs781112676 | in-del | -/TTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206573 | TTTTGTTTTGTTTTG[-/TTT]TTAAAGAGACAGGGT | 89970 |
rs781143259 | in-del | -/AT | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240363 | ACACACACACAAAAA[-/AT]ATATATATATATATA | 89970 |
rs781291597 | snp | C/T | 1.66164e-05 | 0.00288235 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238976 | TCTCATATTTCATGA[C/T]ACATGTGAAGAGGCA | 89970 |
rs781319159 | in-del | -/AG | 1.6477e-05 | 0.00287024 | frameshift-variant | RSPRY1 | GRCh38.p7 | 16:57209127 | AGTTATTCCACTGGA[-/AG]ATCCACTGGGACCAG | 89970 |
rs781320029 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217075 | AAATGTCCGTTTCCA[C/T]TTCCAGACTCATTTC | 89970 |
rs781339219 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237178 | AGATGGAGTCTTGCT[C/T]TGTCGTCCAGGCTGG | 89970 |
rs781359677 | snp | C/G/T | 1.65729e-05 | 0.00287857 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220718 | TAGAAACATGAACAC[C/G/T]CTTTCTTTTGCAGTT | 89970 |
rs781362996 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194734 | TCTGCAGTCCTATTT[C/T]CAAAGAAAAGAAAGT | 89970 |
rs781405457 | snp | A/G | 4.95823e-05 | 0.00497882 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204665 | ACTACCTAAATGATC[A/G]TCTTTGGTTGGGCCG | 89970 |
rs781447763 | snp | A/C | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205681 | TCAGTAGTTAAGAGC[A/C]CAAAGCTTAGAACCA | 89970 |
rs781500893 | in-del | -/CGC | | | utr-variant-5-prime, upstream-variant-2KB, cds-indel | RSPRY1, FAM192A | GRCh38.p7 | 16:57186403 | GTCACAAAGGAGTCG[-/CGC]CGCCGCCGCCGCCCC | 89970 |
rs781501203 | snp | C/T | 1.75342e-05 | 0.00296087 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235266 | AAGTTTCATACTGTT[C/T]TTAAATTGCTAGTTC | 89970 |
rs781569971 | snp | C/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187348 | GAGACCGAGGCGGTC[C/G]GCTGAGACTCCGAGG | 89970 |
rs781593330 | snp | C/T | | | upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186267 | GAGAGGGCTTGCCAC[C/T]GAGGAAGGGGCGTTT | 89970 |
rs781644655 | snp | C/T | 8.25239e-05 | 0.00642302 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208054 | CTTGAATTTTTTTTT[C/T]CAGTGATCAGGAACC | 89970 |
rs781766249 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226230 | TTTGAAGTCTGCTAC[A/T]TGCAAGAAAGGTATT | 89970 |
rs796194500 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215079 | ATGGGTAATGAGAGC[C/T]GGGGTGTCATGAAAG | 89970 |
rs796202142 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199906 | GTTTGTTTTTTTTTT[-/T]CTTTTTCTTTTTTTT | 89970 |
rs796224677 | in-del | -/AC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231769 | TACATCTTTTAGCAG[-/AC]TCGGCTTTATTGAAA | 89970 |
rs796307558 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195665 | AATTGTGTGACTAGC[-/T]TTTTTTTTTTTTGTC | 89970 |
rs796362080 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189767 | GGCCAATTTTTGCAC[-/T]TTTTTTTAAGACAGG | 89970 |
rs796396292 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201040 | CCCTCCCGGATGGGC[A/G]GCTGGCCGGGCGGGG | 89970 |
rs796588061 | in-del | -/TA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216087 | TTTTTTTTTTTTTTT[-/TA]TCTTTTGTTGTTTTT | 89970 |
rs796611328 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199839 | TATCAGTGAAATTTC[-/T]TTTTTTTTTTTTTCC | 89970 |
rs796664695 | in-del | -/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216070 | TCTGCAGGGGAATGA[-/TT]TTTTTTTTTTTTTTT | 89970 |
rs796711758 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223393 | TTCTGTTCAGGTAAC[C/G]TACAGAACAGTTTGT | 89970 |
rs796742873 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197538 | CTTTAAAGTATTTAC[A/C]GTTTTTTTAAAAGCC | 89970 |
rs796776400 | in-del | -/A | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185962 | ATGAATGAAAGAAAG[-/A]AAAAAAAAAAAGAAA | 89970 |
rs796908329 | in-del | -/AA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235094 | GACCCCTGTTGACAA[-/AA]TGTATTTCAAATTGC | 89970 |
rs796918330 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211267 | GACCTTGTCTCTGTT[-/A]AAAAAAAAAAAAAAA | 89970 |
rs796966453 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236872 | CAAGGATGGTACAAT[-/T]ACAGAAATCTTAGGC | 89970 |
rs797002504 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199913 | TTTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 89970 |
rs864309651 | in-del | -/A | | | frameshift-variant | RSPRY1 | GRCh38.p7 | 16:57230716 | ATCCTCTAGGAGATA[-/A]CAGTAGGATTTCTGT | 89970 |
rs864309652 | snp | G/T | | | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204779 | GCCGCTACTACCATG[G/T]GTAATTCCTGTATCT | 89970 |