| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs715040 | snp | G/T | 0.189261 | 0.242509 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214567 | AATACCCACTGATAC[G/T]TGCTTAAAACACTTA | 89970 |
| rs918711 | snp | C/G | 0.460477 | 0.134905 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213664 | AGCACATGGGAGAGT[C/G]CAAACCAGTAGCCAC | 89970 |
| rs950003 | snp | C/T | 0.1652 | 0.235179 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220475 | CATATAGAAATGCTA[C/T]TGATTTTTGTCTGTT | 89970 |
| rs958148 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223049 | TTGGATCAGGGAAGA[A/G]TGTTTGTTTTTAAAG | 89970 |
| rs1132814 | snp | A/C | 0.0547245 | 0.156101 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185949 | TTCTTTCTTTCATTC[A/C]TTCCTTCCTCTGTTT | 89970 |
| rs2288006 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230957 | GGGATAGTTTTAGGT[A/C]TGATCAAATGGGTTC | 89970 |
| rs2399623 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210667 | gcagtgagctgagat[C/T]gtgctactgcactcc | 89970 |
| rs3054336 | in-del | -/CCCT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210048 | cctccctccctccct[-/CCCT]tcctcccttcctccc | 89970 |
| rs3055196 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199852 | TATCAGTGAAATTTC[-/T]TTTTTTTTTTTTTCC | 89970 |
| rs3214478 | in-del | -/A | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239040 | GTTGAAAAGAAAAAG[-/A]AAAAAAAAACTCTCT | 89970 |
| rs3214479 | in-del | -/AG | 0.479984 | 0.0980171 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231770 | GTTTCAATAAAGCCG[-/AG]TCTGCTAAAAGATGT | 89970 |
| rs3217258 | in-del | -/CT | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239050 | AAAAGAAAAAAAAAA[-/CT]CTCTAATCAGTTGTA | 89970 |
| rs4238792 | snp | C/T | 0.175576 | 0.238665 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201824 | ACCAGTCAGGCGTGG[C/T]GGTGCGCGCCTGCAA | 89970 |
| rs4238793 | snp | C/T | 0.174932 | 0.238463 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201864 | CTCGGCAGGCTGAGG[C/T]AGGAGAATCAGGCAG | 89970 |
| rs4287561 | snp | C/T | 0.175576 | 0.238665 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210075 | tcccttccttccttc[C/T]ttccttccctttcct | 89970 |
| rs4330777 | snp | A/G | 0.482309 | 0.0923707 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201732 | gaggccaaggctggc[A/G]gatcactcgcggtta | 89970 |
| rs4503784 | snp | A/C | 0.224412 | 0.248687 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201690 | cactgagtgaacgcg[A/C]ctccgtctgccatcc | 89970 |
| rs4784780 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196675 | AGTATAGGTTATAGA[A/T]AAGTAAAAATTACTT | 89970 |
| rs4784782 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214834 | aggagttcaagacca[A/G/T]cctggccaacatggc | 89970 |
| rs4784783 | snp | C/G | 0.237303 | 0.249677 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216735 | TAAAAAAAAGGAAAA[C/G]AAAATAGTCAAAGCT | 89970 |
| rs5817090 | in-del | -/TCCC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210027 | TCTTCTTTCTTTCTT[-/TCCC]TCCCTCCCTCCCTCC | 89970 |
| rs5817091 | in-del | -/A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223001 | AAATACTGTTTTTTT[-/A/T]ATCCTCCAGATCACT | 89970 |
| rs6499869 | snp | A/C | 0.0569829 | 0.158885 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192564 | ATTTTTTAGTAAATT[A/C]TTTGAATGCTGAAAG | 89970 |
| rs6499870 | snp | A/G | 0.342358 | 0.232314 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192769 | GAAGTGCAGTGGTGC[A/G]ATCATGGTTTACTGC | 89970 |
| rs6499871 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193044 | AACCAGAAAAAAATA[C/T]CTACTTTCAAAGGTG | 89970 |
| rs6499874 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221761 | TGATTATTACCTTGA[A/G]TTGAAGCTCTTAAGA | 89970 |
| rs7186799 | snp | A/C | 0.456803 | 0.140473 | upstream-variant-2KB, missense | RSPRY1, FAM192A | GRCh38.p7 | 16:57186104 | CTCCCCGGGAGCCCG[A/C]TGGAAATCCGGTACC | 89970 |
| rs7190847 | snp | A/G | 0.479824 | 0.098392 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199125 | GAGGTAGTTACATAT[A/G]TACTGATATAGAAGG | 89970 |
| rs7195007 | snp | A/G | 0.319616 | 0.240112 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208451 | TGCCCAGGCTGGAGT[A/G]CAGTGGCACGATCAC | 89970 |
| rs7197204 | snp | G/T | 0.479744 | 0.0985793 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187953 | GAAATTTTCCTCTAA[G/T]TAATTTGATCTCAAC | 89970 |
| rs7202405 | snp | A/G | 0.084728 | 0.187577 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209880 | gggtttcatcatgtt[A/G]cccaggctggtcttg | 89970 |
| rs7206038 | snp | C/T | 0.10447 | 0.203276 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221451 | TGAAAATGGGAGCAG[C/T]GGCAGTTTGCTTTTT | 89970 |
| rs7404384 | snp | G/T | 0.185472 | 0.241529 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210675 | ctgagattgtgctac[G/T]gcactccagcctggg | 89970 |
| rs8047412 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189155 | agcaccacccgtgcc[C/T]ggctaatttttgtat | 89970 |
| rs8048889 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214082 | TTTTATTTGCAGGTG[G/T]TTCCCGAGTGCTTAT | 89970 |
| rs8058218 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212864 | gtggtccgcccgcct[C/T]ggcctcccaaagtgc | 89970 |
| rs9921220 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210329 | aagggatcctcccac[C/T]ttggcttctcaaagt | 89970 |
| rs9927890 | snp | A/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208400 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 89970 |
| rs10153056 | snp | C/T | 0.321769 | 0.239477 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197894 | ATGCCCAGCTAATTT[C/T]TTAATTTTTTCTGTA | 89970 |
| rs10153103 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196034 | TCAAAAAAAAAAAAA[A/T]ATATATATATATATA | 89970 |
| rs10221126 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207958 | CATTTGTGTTCATTT[C/T]TTCTGTCCCTTTTTA | 89970 |
| rs11076181 | snp | A/G | 0.479177 | 0.0998894 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186833 | TCCTGGTACCGATGG[A/G]GTCCTGACCTACTCA | 89970 |
| rs11383644 | in-del | -/A | 0.0182019 | 0.0936463 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185906 | TCGCTCTTAAAAAAG[-/A]AAAAAAAAATGAAAG | 89970 |
| rs11391063 | in-del | -/T/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216070 | TCTGCAGGGGAATGA[-/T/TT]TTTTTTTTTTTTTTT | 89970 |
| rs11546963 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186364 | CCGTGGCCTCGCGTC[A/C]ATCTTTGCCGTTCTC | 89970 |
| rs11643790 | snp | A/C | 0.317692 | 0.240661 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227234 | TCTCTCATCATCCAG[A/C]AAGCTTAGAATCCCA | 89970 |
| rs11645163 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201530 | gggcggccaggcaga[A/G]acactcctcacttcc | 89970 |
| rs11859493 | snp | A/G | 0.2776 | 0.248472 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213742 | TTAACTGTGAAATGG[A/G]GCTAGTACTATTTTC | 89970 |
| rs11860893 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202056 | gccgagcaggatagc[C/T]cacacccgtaatccc | 89970 |
| rs11861071 | snp | G/T | 0.234692 | 0.249531 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212187 | ACTGTGACATGTGCC[G/T]GTAGTCCCAGCTACG | 89970 |
| rs11867111 | snp | A/G | 0.00950871 | 0.068293 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231370 | CATGAATCTTATGAG[A/G]AATTAAACAATTTAT | 89970 |
| rs12149078 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219433 | tgagtaccttttcat[A/G]tatctgtttgccatt | 89970 |
| rs12445335 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199678 | TATATTTTAAGGTTT[C/T]TAGATAAAGATTTTT | 89970 |
| rs12596783 | snp | A/G | 0.0599851 | 0.162463 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186977 | ACGCCTTGGGATAGA[A/G]AGAGAATGGGGCTAG | 89970 |
| rs12597799 | snp | A/C | 0.16618 | 0.23553 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236077 | CCAGCTGTGATTAAT[A/C]CTCCCTATTACTTCT | 89970 |
| rs12917854 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218768 | tgagacggagtctcg[C/T]tctgtcgcccaggct | 89970 |
| rs12928007 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229750 | tcactctgtcaccca[G/T]gctggagtgcagtgg | 89970 |
| rs13331601 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236999 | gtgaaaccccgtctc[C/T]actacaaatacaaaa | 89970 |
| rs13333086 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208378 | GAGAGGAGATtattt[A/T]tatatatatatatat | 89970 |
| rs13336686 | snp | C/T | 0.479095 | 0.100076 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223037 | GGCTGTTGGTTTCTT[C/T]AAAAACAAACACTCT | 89970 |
| rs13339133 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230006 | caccacgccctgccC[C/T]ttttttttttttttt | 89970 |
| rs16967424 | snp | A/G | 0.241627 | 0.24986 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185135 | GAACTAACCAGTCGG[A/G]CTACCCGAGCGTGCG | 89970 |
| rs16967444 | snp | C/G | 0.161596 | 0.233848 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186762 | GGTCGCCCTTCTGAG[C/G]AGGCTGCGGCTAACA | 89970 |
| rs16967743 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207893 | CACATATGGTATACA[G/T]TCATCCTTACAGGTC | 89970 |
| rs16967799 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218008 | CATTTGTTTGATTGA[C/T]CTTCAAATGGCAGTG | 89970 |
| rs16967855 | snp | G/T | 0.237303 | 0.249677 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225023 | TCAGCGTTTGAAAGG[G/T]GTGGCAAGGCATTCT | 89970 |
| rs16967938 | snp | A/G | 0.204189 | 0.245767 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232542 | TATCTATCATACCCC[A/G]TTCTTTTTCATCTAG | 89970 |
| rs16968010 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238644 | TATGCTGTGCACATA[C/T]AGAGTGTCTGAAAGA | 89970 |
| rs17313871 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193101 | AAGGGAAATGTCAGA[A/G]TCATCCAGTGCTTTT | 89970 |
| rs17313981 | snp | A/G | 0.460925 | 0.134204 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207258 | GTACCTGAAATGACC[A/G]TACTAATTCCCATAT | 89970 |
| rs17373185 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194096 | TGCACATTTCAGTGT[A/G]TGTAAATTCGACTCC | 89970 |
| rs28519401 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202590 | AGAATGTGTTCTTTT[A/T]AAAAGCTATTTCCAG | 89970 |
| rs28588503 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194471 | TCTTTAACACACTTA[C/G]GGAAAAATCCGAAAA | 89970 |
| rs28667327 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208402 | TATATATATATATAT[A/T]TTTTTTTTTTTTTGA | 89970 |
| rs34077526 | in-del | -/G | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184465 | CGATACTTGATTTTA[-/G]GACAAAACAATCTTA | 89970 |
| rs34138044 | in-del | -/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208302 | AATGCATATTATACC[-/TT]TTTTTTTTTTTTTTT | 89970 |
| rs34232154 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193642 | AATTACAGGCACACG[-/C]CCACTGTGCCTGGCT | 89970 |
| rs34368338 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228273 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 89970 |
| rs34387182 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202425 | TAGAAATTCATTTCA[-/G]GGGACCCTTTAAAGA | 89970 |
| rs34412473 | snp | A/G | 0.0183909 | 0.0941129 | intron-variant, synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57207617 | TCAAAATGAAGATGC[A/G]TATATAGGCCCTTGC | 89970 |
| rs34463357 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233504 | GCCTCCTGAGTAGCT[-/G]GGGACTACAGGCATG | 89970 |
| rs34703483 | in-del | -/T/TA | 0.16976 | 0.236773 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196033 | TCAAAAAAAAAAAAA[-/T/TA]AATATATATATATAT | 89970 |
| rs34711407 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231936 | ATGCCTGCTTTACTT[-/C]CCTTGTGAGATGAAT | 89970 |
| rs34754718 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233310 | CATACCCACTCTCAG[-/T]CTACAAGTCATCCAC | 89970 |
| rs34766667 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202952 | TTTCTTCTATGTTTT[-/C]CCCTGTAGCAGTAAT | 89970 |
| rs34871304 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186425 | CCGCCGCCCCCTCCC[-/T]TCCGGTGGGCCCGGG | 89970 |
| rs34936184 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235718 | GAGCAGTTGGGCAAT[-/G]GTGGCGTCCTGGCCA | 89970 |
| rs34957747 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193077 | TTTCTTAAAGATCCT[-/C]CAGTGCATAAGGGAA | 89970 |
| rs35236945 | in-del | -/A | | | frameshift-variant | RSPRY1 | GRCh38.p7 | 16:57231198 | CAGCTAGTTTCATGT[-/A]CATATCAACAATGTG | 89970 |
| rs35325134 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190192 | GGGCAACATGGCAAA[A/C]CCCCATCTCTACAAA | 89970 |
| rs35346032 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208724 | TTTGTTCCTTAGTTT[-/C]CCTAAGTATCATTCT | 89970 |
| rs35358243 | snp | G/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237690 | CTTTATTTTTTTATT[G/T]TTATTTATTTATTTA | 89970 |
| rs35398050 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186367 | GGCCTCGCGTCCATC[-/T]TTTGCCGTTCTCTCG | 89970 |
| rs35690831 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190718 | AAGGAGTGAATATTT[-/C]CCCTTTGGTTTATCA | 89970 |
| rs35749950 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236980 | AGACCAGCCTGCCAA[-/G]ACAGTGAAACCCCGT | 89970 |
| rs36021515 | in-del | -/T | 0.186736 | 0.244482 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222994 | AAGACTTAAATACTG[-/T]TTTTTTTATCCTCCA | 89970 |
| rs36062959 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236974 | AGTTGAGACCAGCCT[-/G]GCCAAACAGTGAAAC | 89970 |
| rs36083992 | in-del | -/AATAT/T | 0.16976 | 0.236773 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196034 | CAAAAAAAAAAAAAA[-/AATAT/T]ATATATATATATATA | 89970 |
| rs55656203 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234847 | AGAGCACTGGACTTA[A/G]AACTAAAGGATTTTA | 89970 |
| rs55701001 | in-del | -/ATATATAT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202900 | TATATATATATATAT[-/ATATATAT]CTGAAGACTTTCTGT | 89970 |
| rs55876719 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214906 | TGGTGGCATGTGTGT[A/G]TAGTCCCAGCTACTC | 89970 |
| rs55931785 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224920 | TCAGGACATTAGAAG[A/G]TGAAGATAGAAAAGA | 89970 |
| rs55960976 | snp | C/G | 0.0941369 | 0.195465 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234115 | GACCTATTTCCTACC[C/G]TCTCCCGTTTTCTCA | 89970 |
| rs56031703 | in-del | -/A | 0.463881 | 0.12944 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198383 | CTCAAAAAAAAAAAA[-/A]TTGTACTAAATGGAA | 89970 |
| rs56061089 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189137 | TAACTGGGATTACAG[A/G]CAAGCACCACCCGTG | 89970 |
| rs56208338 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228293 | AAAAAAAAAAAAAAA[-/A]GGAAAGCAGGAATTT | 89970 |
| rs56855576 | in-del | -/AG | 0.237303 | 0.249677 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225083 | GTTTTGTTTTGAGAC[-/AG]AGTCTCGCTCTGTCA | 89970 |
| rs56872751 | snp | A/G | 0.17461 | 0.238362 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191193 | TGAAGAATTGTTTTC[A/G]CTCTTGTGTTCCCTT | 89970 |
| rs57105340 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228373 | AAAAAAATCAGAAAA[-/A]GCCAACAGGAACACT | 89970 |
| rs57401562 | snp | A/G | 0.230603 | 0.249246 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236895 | TCTTAGGCTGGGCAC[A/G]GTGGCTCACACCTGT | 89970 |
| rs57449156 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200638 | CCCTCACCTCCCGGA[A/C]GGGGCGGCTGGCCGG | 89970 |
| rs57561217 | snp | C/T | 0.237303 | 0.249677 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225257 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 89970 |
| rs57564723 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200661 | CTGGCCGGGCGGGGG[A/G]CTGACCCCCCCACCT | 89970 |
| rs57769187 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193571 | GATCTCGGCTCACTG[C/T]AACCTCCACCTTCTG | 89970 |
| rs57872505 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195314 | ATCAGGAGTTCAAGA[C/T]CAGCCTGGTGAACAT | 89970 |
| rs57952896 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200800 | GGGGCTGGCCCCCCC[-/C]ACATCCTTCCCGGAC | 89970 |
| rs58040707 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232294 | TGTCTCAGTGGTTCA[A/G]TAGTTTCCAGATGAA | 89970 |
| rs58392156 | snp | A/C | 0.161924 | 0.233971 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223796 | TAAATAAATAAATAT[A/C]TTTTGCTTTTTTGTG | 89970 |
| rs58714624 | snp | A/G | 0.00489116 | 0.0492103 | missense | RSPRY1 | GRCh38.p7 | 16:57227432 | AGAAGTAAGCCTCAC[A/G]TACACCCATGCTGGA | 89970 |
| rs58871276 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200652 | ACGGGGCGGCTGGCC[A/G]GGCGGGGGGCTGACC | 89970 |
| rs59156529 | in-del | -/AA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228292 | AAAAAAAAAAAAAAA[-/AA]GGAAAGCAGGAATTT | 89970 |
| rs59228011 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190230 | AAAAATTAGCCCAGC[A/G]TGGTGGCACATGCAG | 89970 |
| rs59474456 | in-del | -/ATATATATAT/ATATATATATATATATATATAT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202907 | TATATATATATATAT[lengthTooLong]CTGAAGACTTTCTGT | 89970 |
| rs59693430 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222139 | AAAGCCCCTTGGATT[-/T]ATTTTGTTAATCTAA | 89970 |
| rs59857329 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194978 | TTGATTATTTTTTTT[-/T]GTCTCAGAGCAGCTT | 89970 |
| rs59897690 | snp | C/T | 0.171704 | 0.237423 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221892 | TTAGTTATTTATCTT[C/T]TGTTATAGAAAGCTA | 89970 |
| rs59968957 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191445 | CTTAATACTTTTTTC[A/G]CCCAGGAAGTCTGTC | 89970 |
| rs60180096 | in-del | -/A/T/TA/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216087 | TTTTTTTTTTTTTTT[-/A/T/TA/TT]ATCTTTTGTTGTTTT | 89970 |
| rs60516507 | snp | A/G | 0.46137 | 0.133501 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238262 | TTTCTCTAAACTCTA[A/G]GTTTAATTTGCTCAA | 89970 |
| rs60653561 | snp | C/T | 0.00488784 | 0.0491938 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57227371 | TGGGGATGATGAATA[C/T]TCCTGTGCGTATGAT | 89970 |
| rs61132783 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199896 | TGTTTTTTTTGTTTG[-/T]TTTTTTTTTTCTTTT | 89970 |
| rs61336216 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208398 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 89970 |
| rs61476400 | in-del | -/T | 0.230603 | 0.249246 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236871 | GCAAGGATGGTACAA[-/T]TACAGAAATCTTAGG | 89970 |
| rs61614358 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222212 | TTTAGAAGTGATCCA[A/G]CAAAATCAAGCTAAA | 89970 |
| rs61746362 | snp | A/G | 0.0253123 | 0.109615 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204737 | ACTCTCGAAGAGCAC[A/G]TAGCCCACTTCCTAG | 89970 |
| rs62037358 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189278 | TGGGATTACAGGCAT[G/T]AGCTACTGTGCCTGG | 89970 |
| rs62037359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214594 | CTTACCTTACTCTCA[A/G]TGAGCACTCTGGGGA | 89970 |
| rs62038960 | snp | A/G | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215483 | GTAGCAGTAGGGAAA[A/G]CACAGCTATGAGAAG | 89970 |
| rs62038962 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226686 | GCCATCTTGGTTTTG[G/T]TGGGTTTTGGCCAGC | 89970 |
| rs62038963 | snp | C/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228587 | CCCCTGTAATTTCTC[C/T]AGAGATTTTTTAAAA | 89970 |
| rs66520525 | snp | A/G | 0.480697 | 0.0963277 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218669 | AAATGACAGGATCTC[A/G]TTCTTTTTTGTGGCT | 89970 |
| rs67407530 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208400 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 89970 |
| rs71152240 | in-del | -/GCCTCCCTCGCGGAAGGGGCGGCTGGCCAGGCGGGGGACTGACCCCCC | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200671 | GGGGGCTGACCCCCC[lengthTooLong]CACCTCCCTCCCGGA | 89970 |
| rs71387156 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185936 | GGAAGAAAGAAAGAA[A/C]CAGAGGAAGGAATGA | 89970 |
| rs71387157 | snp | A/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207949 | CTTTCCTTACATTTG[A/T]GTTCATTTCTTCTGT | 89970 |
| rs72121349 | in-del | -/TATATATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202879 | TTTATTACATATGAT[-/TATATATA]TATATATATATATAT | 89970 |
| rs72778732 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191119 | AATACCTTACTCAGC[A/G]AGTATATTACCTCAT | 89970 |
| rs73553028 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204578 | ACTTTCTTTGGCATT[A/C]AGTTGTTAAAAACAA | 89970 |
| rs73553049 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227210 | TAGTATTTTCAAAAA[A/C]CCATGAGCTCTCTCA | 89970 |
| rs74021613 | snp | A/T | 0.0240643 | 0.107019 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184481 | GACAAAACAATCTTA[A/T]CAACATATTCTATAG | 89970 |
| rs74021617 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205151 | ATATTTTAATGCTCC[A/G]CTGATGGCAGAGTAA | 89970 |
| rs74021619 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222168 | AAATAATAGCCCCCC[C/G]CTCCAATATGTAAGA | 89970 |
| rs74246277 | snp | A/G | 0.234692 | 0.249531 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199173 | GCAAATCATAGAGCA[A/G]TATTTATGGCTTCAT | 89970 |
| rs74410599 | snp | A/C | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228275 | GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA | 89970 |
| rs74432679 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231428 | AAATTTTGAAAACCT[A/G]AGTAAAATGGATGAC | 89970 |
| rs74471685 | snp | C/G | 0.163236 | 0.234461 | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186428 | GCCGCCCCCTCCCTC[C/G]GGTGGGCCCGGGAGG | 89970 |
| rs74485691 | snp | A/C | 0.177824 | 0.239355 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186463 | GAAAGTCAGTGCCAC[A/C]GCCCGACCGCGCTGC | 89970 |
| rs74547421 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203746 | TACCTGGCACAAGGT[C/G]CTTAGTCAGTATTTT | 89970 |
| rs74630199 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217938 | TGGATTTTGTTCATA[C/T]AAAATTATATTCTAG | 89970 |
| rs74701001 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227888 | GGTAGAGGATATAAC[C/T]TCTGGAAGGATTTGA | 89970 |
| rs74745901 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217705 | CCTCATGTCTGCACT[A/C]AAAAAGTATTGGATT | 89970 |
| rs74939379 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208920 | TTACTCCACCACGAT[A/G]ACTAGCAATTGATGA | 89970 |
| rs75045815 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192710 | TTTTCCAGAGACTCT[C/T]TTTTTTTTTTTTTTT | 89970 |
| rs75053752 | snp | C/T | 0.16846 | 0.236329 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237938 | TTTTTAATGGTGACA[C/T]ATAGGAAGCATTTCA | 89970 |
| rs75114930 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196340 | ACTGGACAAGGAAAT[A/T]AACATTTTTGACCCA | 89970 |
| rs75416141 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234496 | GTCCTCTGTTCACTG[C/T]TGAATCTCTAGGGCT | 89970 |
| rs75631671 | snp | A/T | 0.189261 | 0.242509 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212550 | TATTTCCCATCAATG[A/T]TATCATTAGGGTACA | 89970 |
| rs75637899 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230907 | CATTTATATATGCAA[C/T]TGTGATGAGAAATTG | 89970 |
| rs75638803 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235019 | TGAACAAAGTTTAAG[A/G]AATATATGTCACAGG | 89970 |
| rs75660456 | snp | A/G | 0.00300776 | 0.0386631 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213150 | TTGTTTGACATTAAA[A/G]GGAAATTTGTACTGT | 89970 |
| rs75668550 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211583 | CAACAACAACAACAA[A/C]AAAAAGTTAAAACTG | 89970 |
| rs75813034 | snp | C/T | 0.161924 | 0.233971 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187649 | ATAAAAGTGAAGGCA[C/T]TTTCTAAAATGTAAA | 89970 |
| rs75872548 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211372 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAT | 89970 |
| rs75899168 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204034 | TAACAACAAACGTCT[A/G]TAATTATTTTATTTA | 89970 |
| rs76072267 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196334 | CATTTTACTGGACAA[G/T]GAAATTAACATTTTT | 89970 |
| rs76086740 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205384 | CCTCAGATTCAAGGT[A/G]AGTTGTTTTACCAAG | 89970 |
| rs76203784 | snp | G/T | 0.17461 | 0.238362 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205924 | TTATGTGTTCTTTTT[G/T]CTTCAGGCCCTGCTA | 89970 |
| rs76217477 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207462 | TTAAAGATTTCTGGG[A/T]TCACACCACTGAATT | 89970 |
| rs76245323 | in-del | -/AA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197515 | TTATTTAAAAAAAAA[-/AA]GTCTGGCTTTAAAGT | 89970 |
| rs76694635 | snp | G/T | 0.1652 | 0.235179 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208228 | TCCAAAAATACAGCA[G/T]ACATAACAATGAAAA | 89970 |
| rs76737062 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199533 | GTATATAATAATAGA[C/T]ATGGAGGCAAACATA | 89970 |
| rs76752987 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184627 | ACTGACCCTGTACGT[A/G]CATCGCACTTGTTAC | 89970 |
| rs76859827 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218720 | TATGTGCCACATTTT[-/C]TTTTTTTTTTTTTTT | 89970 |
| rs77056538 | snp | A/G | 0.0225045 | 0.103662 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186775 | AGGAGGCTGCGGCTA[A/G]CAGGGCCCAGGTGAG | 89970 |
| rs77316426 | snp | A/T | 0.021333 | 0.101051 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221523 | ATTTGCTCAATAATC[A/T]TTTCTTGGGCAGAGC | 89970 |
| rs77353290 | snp | C/T | 0.17461 | 0.238362 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187525 | GAGTGACTTAACCTC[C/T]TTAAGTCTCTACTGT | 89970 |
| rs77540669 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236270 | TTTGAGCTCTCTGGT[C/G]CTGTGGTCTTGCACA | 89970 |
| rs77602358 | snp | C/T | 0.168135 | 0.236216 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188401 | AAGAGACTTGTGTCC[C/T]TGTATGACATTTTAC | 89970 |
| rs77694385 | snp | A/G | 0.16846 | 0.236329 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207833 | TGTCTGTATCCACCT[A/G]CCCATTTTGTCTGTG | 89970 |
| rs77706973 | snp | A/G | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230882 | CTCTAGGAAAAAAAA[A/G]GTCTTTGTCCATTTA | 89970 |
| rs77902461 | snp | A/G | 0.0364509 | 0.129988 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184452 | TTTTTTAAACTTGTC[A/G]ATACTTGATTTTAGA | 89970 |
| rs78023665 | snp | A/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229861 | CAGGCACCTGCCATT[A/T]ACACCCGGGTAATTT | 89970 |
| rs78101427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222372 | TAGCTGAGACTACAG[A/G]CACATCCCATGGTGA | 89970 |
| rs78105095 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217704 | GCCTCATGTCTGCAC[A/T]CAAAAAGTATTGGAT | 89970 |
| rs78110752 | snp | C/T | 0.248755 | 0.249997 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205804 | AATGGGGGGATAATA[C/T]TGTTCCCACAAGGAT | 89970 |
| rs78141999 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204190 | TTGAAAAAAAATGCA[C/T]ACATCCTTCTAATGT | 89970 |
| rs78189776 | snp | C/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210015 | AATTGCTTTTTTTTC[C/T]TCTTTCTTTCTTTCC | 89970 |
| rs78247072 | snp | A/C | | | missense | RSPRY1 | GRCh38.p7 | 16:57220789 | TGAGTAGCATTAGGG[A/C]CATGCTGAATAGCAA | 89970 |
| rs78339973 | in-del | -/ACAAA | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184424 | TACAGAAAACCAAAC[-/ACAAA]ACAATCTTTTTTTTA | 89970 |
| rs78350884 | snp | A/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197229 | CTCTGTAAAAAAAAA[A/T]TACCATGAATGACAG | 89970 |
| rs78421029 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216489 | TTGGGAAGCTAAGGC[C/T]AGAGCATTGCTTCAG | 89970 |
| rs78582539 | snp | A/C/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217707 | TCATGTCTGCACTCA[A/C/G]AAAGTATTGGATTTT | 89970 |
| rs78689993 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204397 | AAAATAACCAAAGAT[A/C/T]ATTCTTCATTAGAAT | 89970 |
| rs78758520 | snp | A/G | 0.00455626 | 0.0475118 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205060 | AAAAGTGTTCTGCCC[A/G]GAACCATGACTTTAG | 89970 |
| rs78800122 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231806 | TTTTTATGTGGTTTC[A/G]ACTGTGTGGCAAAGA | 89970 |
| rs78875982 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200432 | TGAGTACATCTCCCA[A/G]ACGGGGTGGTGGCCG | 89970 |
| rs78999802 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188800 | GGATTACAGGCGTGA[A/G]CCACTGTGTCTGCCT | 89970 |
| rs79009676 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224036 | CTTCGAGAAAATGAC[C/T]CTGGCTATCTCAGAC | 89970 |
| rs79015752 | snp | A/C | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198384 | GCAAGACTCCGTCTC[A/C]AAAAAAAAAAATTGT | 89970 |
| rs79175879 | snp | A/G | 0.168135 | 0.236216 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211022 | GTATTTGTATCTCAG[A/G]TGGCGATCTTTATTC | 89970 |
| rs79355163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196776 | AGAATCCCTCTCCCC[C/T]AGGTAATTTAGTTAT | 89970 |
| rs79394528 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222194 | TAAGATCCTGGAATG[A/G]GTTTTAGAAGTGATC | 89970 |
| rs79424226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232495 | GAACTTTAAATTCCT[A/C]TTGGCCAAAGTCTGA | 89970 |
| rs79506069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226264 | CTGATCTGATCTTGT[C/T]ACTGGAAAGGGTCTG | 89970 |
| rs79541240 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204084 | ATGGGTTTAAAGAAA[A/G]GAGTTAATTCATTTT | 89970 |
| rs79602910 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184681 | TCAATAGCTAAAGCA[A/G]CAGCTTGATTCTAAC | 89970 |
| rs79674757 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196805 | ATTTCTGATTAGATA[C/T]GTGCTCATTTTGTAA | 89970 |
| rs79722376 | snp | C/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214945 | GAGGCAGGAATTCAC[C/T]TGAACCCAGAAGGCA | 89970 |
| rs79753197 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224161 | AGGAAGTACAATAGC[C/T]GGTGTTTTAGGGAAA | 89970 |
| rs79819297 | snp | A/C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205549 | CAAGGCACACCTGTA[A/C/T]CTGTTTTGTCTTTTC | 89970 |
| rs79865191 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203349 | ATATTTCTCTTCTAA[A/T]TCCACTGAATTATAA | 89970 |
| rs79932158 | snp | C/G | 0.039522 | 0.134904 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222924 | GGATCATTTCATCTG[C/G]TCGATGAAATTATAA | 89970 |
| rs80046598 | snp | A/T | 0.039522 | 0.134904 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238249 | TAAAGGTGACAGTTT[A/T]CTCTAAACTCTAAGT | 89970 |
| rs80136420 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190928 | GGCCTCTTAGAGAAC[A/G]TTCCGCTTTGTTTCT | 89970 |
| rs80252652 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207461 | TTTAAAGATTTCTGG[C/G]ATCACACCACTGAAT | 89970 |
| rs80302553 | snp | C/T | 0.0130414 | 0.0796907 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205059 | GAAAAGTGTTCTGCC[C/T]GGAACCATGACTTTA | 89970 |
| rs80355333 | snp | A/C | 0.444444 | 0.157135 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216595 | CATGGTGGCATGCAC[A/C]TATGTTCCTAGCTAC | 89970 |
| rs111236108 | snp | A/T | 0.444444 | 0.157135 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209423 | GGCTGGAGTGCAATG[A/T]TGTGATCTTGGCTCA | 89970 |
| rs111290864 | in-del | -/T | 0.478603 | 0.101197 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193492 | GGGTGTTCTGCAGGC[-/T]TTTTTTTTTTTTTCT | 89970 |
| rs111309292 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209713 | GGGTCTCACTTTGTC[A/C]CCCAGGCTGGCGTGC | 89970 |
| rs111387495 | snp | G/T | 0.5 | 0 | missense | RSPRY1 | GRCh38.p7 | 16:57221316 | TGTGCGTTGCACCTT[G/T]TGTGTGGATGCCGGG | 89970 |
| rs111399318 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228221 | GAGGTTGCAATGAGC[C/T]GAGGTTGCGCCACTG | 89970 |
| rs111444290 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232402 | ACATAAGGGTTGCAT[A/G]TGTTCCCGCTCAGGG | 89970 |
| rs111474316 | snp | C/T | 0.480853 | 0.0959518 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208438 | AGTCTCACTCTGTTG[C/T]CCAGGCTGGAGTGCA | 89970 |
| rs111511081 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201645 | CGAGCCGAGATCACG[C/G]CACTGCACTCCAGCC | 89970 |
| rs111529780 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221560 | GTACCAGGTCCCTAA[C/G]AATGATCTACTAAAC | 89970 |
| rs111564653 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210074 | CTCCCTTCCTTCCTT[C/T]TTTCCTTCCCTTTCC | 89970 |
| rs111645158 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205635 | AAGGGCATCCAAGTA[A/G]AAAAAAACATTTAAC | 89970 |
| rs111719801 | snp | C/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227333 | CTTCTGGGCCTTGTC[C/T]CTCTCCAGGAAGGCT | 89970 |
| rs111731958 | snp | A/C | 0.0448719 | 0.142907 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184414 | ATAGTGGAAATACAG[A/C]AAACCAAACACAAAA | 89970 |
| rs111747712 | snp | A/C | 0 | 0 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239494 | ACACAGTCAGTACTA[A/C]AAGCAAAACAGAGAA | 89970 |
| rs111763413 | snp | C/T | 0.234692 | 0.249531 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195793 | TTTGGGAGGCTGAAG[C/T]GGGTGGATCATGAGG | 89970 |
| rs111764656 | snp | A/C | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212924 | TGAGCCTGGGAAAAC[A/C]ACCTGTGTAGTATAT | 89970 |
| rs111782511 | in-del | -/TT | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188991 | TCTGTACTCAGTGAC[-/TT]TTTTTTTTTTTTTTT | 89970 |
| rs111860984 | in-del | -/TTTG | 0.268452 | 0.249318 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188515 | TGTGTTTTTGGTTTT[-/TTTG]TTTGTTTGTTTGTTT | 89970 |
| rs111914755 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199906 | GTTTGTTTTTTTTTT[C/T]CTTTTTCTTTTTTTT | 89970 |
| rs111956096 | snp | G/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210848 | ATGGTGAAACCCTGT[G/T]TCTACAAAAAAATCC | 89970 |
| rs111967613 | snp | A/T | 0.444444 | 0.157135 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209021 | CTCGTGTGACATATT[A/T]TCACATTTTAAAAAT | 89970 |
| rs112032861 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218821 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 89970 |
| rs112052628 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228645 | TTTTGTTGTTGTTAT[A/G]CTTAATACCTTGAAC | 89970 |
| rs112058430 | snp | C/T | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221423 | TCAATCATGTGAGTA[C/T]CCTAGAGAACTGTGA | 89970 |
| rs112095790 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227047 | CCTCTTAAAATGGAG[C/T]CTGATGCCACCAGCC | 89970 |
| rs112122633 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212288 | TGCACAGCAGCCTGG[C/G]AAACAGAGCAAGAGC | 89970 |
| rs112127134 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188114 | CGTTGTTGTGGTAGC[C/T]CTAGACTATAGATTA | 89970 |
| rs112220061 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214687 | CAGACAAGGTAATTA[A/C/G]CCTCCATTTTATCAC | 89970 |
| rs112235615 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234862 | GAACTAAAGGATTTT[A/G]ATTTGATTCCTGACT | 89970 |
| rs112281541 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209764 | CTGCAGCTGCAACCT[C/T]CCTAGGCTCAGGTGA | 89970 |
| rs112286780 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190130 | CACAACACTTTGGGC[A/G]GCCAAGGCGGGAGGA | 89970 |
| rs112362218 | snp | A/G | 0 | 0 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239714 | AAAAATGTTTTACCA[A/G]TGAAGGAGGAATTCT | 89970 |
| rs112371057 | snp | A/G | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229134 | TCTGGATTTTCTCAA[A/G]ACAAAACCCTTAGAA | 89970 |
| rs112384035 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232170 | TGACATAGCTAATGT[C/T]GGACTGGTATGCCCC | 89970 |
| rs112406373 | snp | G/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237409 | TGGCCTCCGAAAAGT[G/T]CTGGGATTACAGGCA | 89970 |
| rs112469574 | in-del | -/T | 0 | 0 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239613 | TTTTTGTTTTTTGGG[-/T]TTTTTTTTTTTTACT | 89970 |
| rs112489672 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210061 | CCTTCCTCCCTTCCT[C/T]CCTTCCTTCCTTCTT | 89970 |
| rs112518312 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201056 | GCTGGCCGGGCGGGG[C/G]GCTGACCCCCACCTC | 89970 |
| rs112529536 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202869 | TTATATATATTTTAT[A/T]ACATATGATTATATA | 89970 |
| rs112586906 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202053 | GGGGCCGAGCAGGAT[A/T]GCTCACACCCGTAAT | 89970 |
| rs112587041 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225514 | ACAAAATCATTGTTG[C/T]ATTCATCAGAACTTT | 89970 |
| rs112596141 | snp | A/G/T | 0.00348739 | 0.0416117 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209046 | AAAAATAGTGACTCC[A/G/T]TCATATAATCTTCTT | 89970 |
| rs112615840 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200676 | GCTGACCCCCCCACC[C/T]CCCTCCCGGACGGGG | 89970 |
| rs112646609 | snp | A/G | 0.5 | 0 | intron-variant, splice-donor-variant | RSPRY1 | GRCh38.p7 | 16:57207686 | TGGCATTTCTCTGAG[A/G]TAAGTATGAAGGTGA | 89970 |
| rs112699961 | snp | C/T | 0.461037 | 0.134028 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208460 | TGGAGTGCAGTGGCA[C/T]GATCACAGCTCAACT | 89970 |
| rs112705000 | in-del | -/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205893 | CAGTAGATGGTAGTA[-/T]TTTTTAAAAAGTTAC | 89970 |
| rs112718122 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226879 | TTCAAGATGGAGTCT[C/T]TCTGGTTTGAATGCC | 89970 |
| rs112722990 | snp | A/G | 0.00500792 | 0.0497884 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220866 | GGTAATGCTTCTACA[A/G]TTGGACCCTTTGGGG | 89970 |
| rs112725750 | snp | A/G | 0.0448719 | 0.142907 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205068 | TCTGCCCGGAACCAT[A/G]ACTTTAGGACTCCTT | 89970 |
| rs112850989 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188292 | CATTTTACTAGTGTT[C/T]GGTTCGTCGTACTTG | 89970 |
| rs112858484 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229189 | TATAGAATTTCAAAG[C/T]TTTTGCTGTATATTG | 89970 |
| rs112880013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192868 | CTATAGGGTCCAAGC[C/T]GCCACTCTGGCTAAT | 89970 |
| rs112899786 | snp | A/C | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236747 | AAGCTGATAAAACTC[A/C]TAAAAAGAAAAAACT | 89970 |
| rs112900730 | snp | A/C | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215119 | CTGATGAAGGTGGAC[A/C]CTCAGCTGGGTCATG | 89970 |
| rs112955905 | snp | A/G | 0.5 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219227 | TTTAGTGTTTTGAGG[A/G]ACCTCCATACTGTTC | 89970 |
| rs113124577 | snp | A/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212654 | GAGCCTTGCTCTGTC[A/G]TCCAGGCTGGAGTGC | 89970 |
| rs113153910 | snp | A/G | 0.0448719 | 0.142907 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185702 | CTCCGGACAAGGAGC[A/G]GGTGCGCGGACTGAG | 89970 |
| rs113156599 | snp | C/T | 0.277867 | 0.248442 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199448 | AGTGAGCCAAGATCG[C/T]ACCATTGCACTCCAG | 89970 |
| rs113195195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204337 | ATTATTGATTGATTG[C/T]GAATTCTGTTATCCA | 89970 |
| rs113305956 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225843 | CAGCACTTTGGGAGG[C/T]CGAGGCGGGCAGATC | 89970 |
| rs113385856 | in-del | -/A | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212898 | TATAGCTTTTGTCTC[-/A]AAAAAAAAAATGAGC | 89970 |
| rs113397620 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229917 | TCACCATGTTGGCTG[G/T]GCTGGTCTCAAACTG | 89970 |
| rs113449687 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237402 | CCTGCCTTGGCCTCC[C/G]AAAAGTTCTGGGATT | 89970 |
| rs113498899 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218947 | TTCACCGTTTTAGCC[A/G]GGATGGTCTCGATCT | 89970 |
| rs113551291 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219835 | ATTTGATTTTTGTAG[A/G]CAATGAGAGATAGGG | 89970 |
| rs113552051 | snp | A/G | 0.5 | 0 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204873 | CAGTACCCACTGCTG[A/G]CACAAGGAGCCAACC | 89970 |
| rs113642823 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224174 | GCCGGTGTTTTAGGG[A/G]AACGATCTGGCCAGC | 89970 |
| rs113678753 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193873 | GAGTTTGAGACCAGC[C/G]TAGCCCACATGGTGA | 89970 |
| rs113691752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228151 | GGTGGCACCCACCTG[C/T]GGTCCCGGCTACTTG | 89970 |
| rs113769369 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199907 | TTTGTTTTTTTTTTT[C/T]TTTTTCTTTTTTTTT | 89970 |
| rs113823354 | in-del | -/A | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228358 | GGTGTGGGAAAAAAA[-/A]TCAGAAAAGCCAACA | 89970 |
| rs113889469 | snp | C/T | 0 | 0 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239255 | AGCAGACAATGCCCT[C/T]CCAAGTACTGAAATC | 89970 |
| rs113948966 | snp | C/G | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206550 | ATAGACTTTGAGAGA[C/G]AGAGTTTTTTTGTTT | 89970 |
| rs113957542 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200477 | TCACTTCCCAGTAGG[A/G]GCGGCAGGGCAGAGG | 89970 |
| rs113970853 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210699 | GCCTGGGCGACAAAG[C/T]GAAACTCTGTCTCAA | 89970 |
| rs114027873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197476 | AACCTCTTCTTTACA[C/T]TTGGTTTTCACAGAT | 89970 |
| rs114100456 | snp | A/G/T | 0.0233517 | 0.105971 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198046 | GATTTAGTCAGATTT[A/G/T]AAAAAAAAATCTGCG | 89970 |
| rs114111266 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227940 | AGAGGATATAACCCA[A/G]CTCTTTCTCCAAGCA | 89970 |
| rs114167820 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221132 | TTGTACTTTTTGTCA[C/G]TGAGGATGGACAGAG | 89970 |
| rs114347995 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199535 | ATATAATAATAGATA[C/T]GGAGGCAAACATATG | 89970 |
| rs114367965 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223275 | AAAAGATTCTAAGTC[C/T]CTGCATAGTGCCTCT | 89970 |
| rs114461508 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190357 | AGCAACACCCTGTCT[C/T]AAATAAATAAATAGG | 89970 |
| rs114663500 | snp | C/T | 0.0622301 | 0.165053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185690 | AGGCTTCGGCTACTC[C/T]GGACAAGGAGCGGGT | 89970 |
| rs114693498 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224348 | GAACACTGTCTTCAT[A/C]CATTTCCCTTAACAG | 89970 |
| rs114713310 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229434 | AGCCTGGGCAACATA[A/T]TGAGACCCCCCATCT | 89970 |
| rs114775953 | snp | A/C | 0.0729998 | 0.176553 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240358 | ACACACACACACACA[A/C]AAAAAATATATATAT | 89970 |
| rs114906548 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227267 | CATTAGGTCAGTGGT[C/T]GTAAAAGACACACTC | 89970 |
| rs114930919 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209847 | GTCTGGCTAATTTTG[G/T]ATTTTTTTTTAGAGA | 89970 |
| rs114948346 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213347 | TTGCTTTAAGAATAA[A/G]GAGCGAGGAAAAGAA | 89970 |
| rs115012681 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227765 | CAGCCATGGCAATAT[C/T]AGGGACACTGGAATT | 89970 |
| rs115137997 | snp | A/G | 0.0252325 | 0.109451 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205155 | TTTAATGCTCCGCTG[A/G]TGGCAGAGTAAATGA | 89970 |
| rs115145904 | snp | C/T | 0.00358779 | 0.0422022 | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240524 | TTCCAAGACATTATA[C/T]TCTCAGACTTTAAGG | 89970 |
| rs115156149 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206889 | ATTTTAAAAGAGAGT[A/G]ACATAGTTATACAAA | 89970 |
| rs115334015 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233751 | ACCTTACTTTCTGCT[A/G]TTTCCACATTCAATC | 89970 |
| rs115476500 | snp | C/G | 0.00246442 | 0.0350162 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57235142 | CAGGCGTCTTGCTCT[C/G]TTGAAGCAAGTCAGT | 89970 |
| rs115498498 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205319 | GCTACAATAGGAAAT[A/G]GTTTCATGAAGGCTC | 89970 |
| rs115732827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227281 | TCGTAAAAGACACAC[A/T]CTCTGTTCCCAGGTC | 89970 |
| rs115919665 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198864 | GAGTTCCCCTCTGCT[A/G]TGGCAATGTTGACAC | 89970 |
| rs116041588 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236014 | GAGTGTGTCTCATTT[C/T]ACCCTTAGCTATACC | 89970 |
| rs116054461 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226314 | GGTTTTTGGACCTCG[C/T]GCAAGAAAGAATTTG | 89970 |
| rs116106888 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191295 | TTTTTTAAGTTTTTA[C/T]TGCTTCATAGTTGTT | 89970 |
| rs116297679 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210788 | TTTGGGAGGCCAAAG[C/T]AGGCAGATTGTTTGA | 89970 |
| rs116308702 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193708 | ATAATGTTCTCTATC[G/T]TGATAGGGTTTGAGT | 89970 |
| rs116399047 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198474 | ATGATAAAGTTTAAG[A/T]ATTTAAGATCCAACA | 89970 |
| rs116707644 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189893 | ACCATGCCTGGCCTC[A/G]TGAGCTTAATTTAGT | 89970 |
| rs116735111 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227887 | TGGTAGAGGATATAA[A/C]CTCTGGAAGGATTTG | 89970 |
| rs116791545 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224196 | CTGGCCAGCATGCAG[C/T]CACCATTGCTGCTGG | 89970 |
| rs116846018 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218451 | TTCATTCTATCTAGC[G/T]ATATTCCCATTAACC | 89970 |
| rs116934773 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238756 | TCATTTTTTTTAAAC[A/C]ATGTATAATTAGTAA | 89970 |
| rs116955990 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207096 | CACTGCAGTGAACAG[C/T]GCAAATATGCATTGA | 89970 |
| rs116956619 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189509 | GCCTGGAGGCTAAAA[A/G]AAAAAAAAGTGTGTT | 89970 |
| rs116974687 | snp | G/T | 0.17138 | 0.237316 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218590 | AGAACACACGAAGTT[G/T]GTCTTTCTGTGCCTG | 89970 |
| rs117154602 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228147 | GTGTGGTGGCACCCA[A/C]CTGCGGTCCCGGCTA | 89970 |
| rs117168204 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217659 | CCTTAATCAAAAAAT[A/C]TGAAATCCTCCATTG | 89970 |
| rs117199678 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240004 | AAAGTGTTAATCCCT[C/T]TCAGGGTCTCTGGTG | 89970 |
| rs117250566 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190651 | GAAGTAGTAAATGCC[A/G]TAACTTGGGCAACAG | 89970 |
| rs117574240 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190885 | TATACAAGGTTAAAT[C/G]AGGAAAAGTTATCTT | 89970 |
| rs117753980 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224070 | AAAGGAATGATTTAG[A/C]AGCCTTTCCGGAGCC | 89970 |
| rs118086940 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233152 | TGGCCCTGTTACTAC[C/T]AACTGGGATTTTATA | 89970 |
| rs137907643 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207836 | CTGTATCCACCTGCC[C/T]ATTTTGTCTGTGGGT | 89970 |
| rs137965233 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237060 | GTAATCCCAGCTACT[C/T]AGGAGGCTGAGACAA | 89970 |
| rs138231513 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, synonymous-codon | RSPRY1, FAM192A | GRCh38.p7 | 16:57186127 | CCGGTACCCTGAAAA[C/T]GAGCCGGAGAGACTT | 89970 |
| rs138267140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224861 | TACCAACTCATGGTG[A/G]CTAGCTTCTAGGAAT | 89970 |
| rs138304750 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228230 | ATGAGCCGAGGTTGC[A/G]CCACTGCACTCCAGC | 89970 |
| rs138307905 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233720 | TCCCTGGCCATAACC[A/G]TAGAGTATCCTTGAC | 89970 |
| rs138328082 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191972 | GAGGGACCTTTTTCC[A/G]TCTTTCCTCACTGCC | 89970 |
| rs138358471 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208175 | AGAAAAGTAGCCACC[-/T]TTTGTTTTTTGTTTT | 89970 |
| rs138413108 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214069 | AATCAATTGTAAATT[G/T]TATTTGCAGGTGTTT | 89970 |
| rs138498140 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193034 | TAGTCTTTCAACCAG[-/A]AAAAAAATACCTACT | 89970 |
| rs138529826 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57205184 | GATAAGATTTGATGT[G/T]TTTGCTTGCTGTCAT | 89970 |
| rs138832424 | snp | A/G | 0.00019883 | 0.00996873 | missense | RSPRY1 | GRCh38.p7 | 16:57230741 | TTCTGTTAGACTTGA[A/G]TGAAAAGCAAATGAT | 89970 |
| rs138838208 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187081 | AGAGGGGATTTCTGG[A/G]CGGTGATGGGAAGAA | 89970 |
| rs138857992 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191446 | TTAATACTTTTTTCG[C/T]CCAGGAAGTCTGTCC | 89970 |
| rs138873673 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219239 | AGGAACCTCCATACT[C/G]TTCTCCATAGTGGCC | 89970 |
| rs138910929 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223855 | GTCTTTCACATATTT[A/C]TCTTTAATCTTTTTG | 89970 |
| rs138912532 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210358 | GTGTTGGGATTATAC[A/G]TGTAAGCCACTGTGC | 89970 |
| rs139028346 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231632 | ACGGAACACTTTCAA[A/T]TTTTTTTTGTGAGAT | 89970 |
| rs139034588 | snp | A/G | 8.23689e-05 | 0.00641698 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204770 | ACTGGAGGTGCCGCT[A/G]CTACCATGGGTAATT | 89970 |
| rs139172950 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211244 | TACCAGCCTGAACAA[C/G]ATAGTGAGACCTTGT | 89970 |
| rs139292948 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236633 | CACAGGTGAACTCTT[G/T]ACAACTTTCAGGGAA | 89970 |
| rs139335192 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239248 | AAACCATAGCAGACA[A/G]TGCCCTCCCAAGTAC | 89970 |
| rs139335272 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195904 | GCACGCACCTGTAGT[C/G]CTGGCTACTCGGGAG | 89970 |
| rs139340196 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237893 | AATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 89970 |
| rs139351965 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225885 | AGAGTTCGAGACCAG[C/G]CTGACCAACATGGAG | 89970 |
| rs139372745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198694 | GGAACTTGACATTCT[C/T]AAATCATTGCCAGTT | 89970 |
| rs139378086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197303 | TCTGAAAGATCATCT[A/G]CTTTGTTCATTTATG | 89970 |
| rs139524254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193455 | TTAAACACAATCTTC[A/G]GTAAGAAGATTGTGG | 89970 |
| rs139563434 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196352 | AATTAACATTTTTGA[C/T]CCAAGAAGAAATGCC | 89970 |
| rs139606229 | snp | A/T | 4.94964e-05 | 0.00497451 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57208075 | ATCAGGAACCTCCCT[A/T]TTCAATGATAACATT | 89970 |
| rs139609273 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235617 | CAGAGGGCAGCCTGG[A/C]CCCTATAGAACAGAG | 89970 |
| rs139706857 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215514 | GTGTCATGTTCAACA[A/G]ATAGACCTTTCCTTA | 89970 |
| rs139743960 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217244 | TTTCAGCATTTTCCT[C/G]TTCAAAAACCTTTAC | 89970 |
| rs139763593 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221989 | ACAGATGTATGATTT[A/C]TTGCCACTTTATACC | 89970 |
| rs139935010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202507 | CTCTTAGTTATCTAC[C/T]CTCTAAAGCGAATCA | 89970 |
| rs139945432 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212054 | CAGTGGTTCATGCCT[A/G]TAATCCCAAAACTTT | 89970 |
| rs139987771 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214921 | GTAGTCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 89970 |
| rs140106927 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218158 | TGTGTTTTACCTTCC[A/G]GGGGGATTATTTTTA | 89970 |
| rs140166449 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225151 | CTGCAACCTCTGCCT[C/T]CCAGGTTCAGGCGAT | 89970 |
| rs140338070 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235854 | TAGCTTTAGTCACGT[A/G]GCTCCACAGGGGTCC | 89970 |
| rs140339084 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190361 | ACACCCTGTCTCAAA[C/T]AAATAAATAGGAAAT | 89970 |
| rs140339510 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189774 | TTTTTGCACTTTTTT[-/T]AAGACAGGGTTACGC | 89970 |
| rs140359404 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194556 | ATTCATGCTATTTGA[C/T]TTAGCCTTTGTGGGG | 89970 |
| rs140372775 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57230796 | GCCTCCTGAAAAGCA[A/G]GTCTTTTCATCTACT | 89970 |
| rs140412396 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234533 | AGTGCCTGGCACACA[A/G]TAAGCCCGTAAGTGA | 89970 |
| rs140473520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238292 | ACATAAAAAGAGCAA[C/G]ATGATTTTTTTCTGG | 89970 |
| rs140565458 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57209176 | CTAGATGAATGTCCA[C/T]TGCCCACTAAAGTAA | 89970 |
| rs140569775 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212835 | GGCCAGGCTGGTGTC[A/G]AACTCTTGACCTTGT | 89970 |
| rs140694492 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193928 | AACATTAGCTGGGTG[C/T]GGTGGCATGTGCCAA | 89970 |
| rs140926092 | snp | G/T | 1.64833e-05 | 0.00287078 | missense | RSPRY1 | GRCh38.p7 | 16:57221287 | GCTCGCTGTGATGCC[G/T]CCTCTTTTGAAAGTG | 89970 |
| rs140975330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203668 | GATGAGAATGGCCAT[C/G]CATGAATTCCTGGAG | 89970 |
| rs140996021 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197667 | CAATTTGGAAAAAAA[C/T]TTAATTTTTGTCTTC | 89970 |
| rs141072645 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209935 | CCCACCTCAGCCTCC[C/T]GAAGTGCTGGCATTG | 89970 |
| rs141117726 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185010 | CTGTGGACACATGAA[C/T]ACACCAAATAACTGA | 89970 |
| rs141180482 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206142 | ACACAATGGCTCATA[A/C]CTGTAATTCCAACAC | 89970 |
| rs141275944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232712 | TAAACCTTCCCAAAC[G/T]CAGATGGCAATGGGC | 89970 |
| rs141307153 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211067 | AATGTTGAGTTGCTT[C/T]GCTGATTTTCTTATC | 89970 |
| rs141350118 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224025 | GAAGCATCTGCCTTC[A/G]AGAAAATGACTCTGG | 89970 |
| rs141402944 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233338 | CACTCACAGCCACTG[C/T]TTCTCCCTCAGTCTT | 89970 |
| rs141427328 | snp | C/G/T | 3.30868e-05 | 0.00406723 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220723 | ACATGAACACTCTTT[C/G/T]TTTTGCAGTTTTAAA | 89970 |
| rs141535938 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204505 | TCATTTTCTTTTAGA[A/G]CTGCCATTGGATGTC | 89970 |
| rs141578418 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209449 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTCCAA | 89970 |
| rs141702855 | snp | A/C | 0.0471551 | 0.14613 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240360 | ACACACACACACACA[A/C]AAAATATATATATAT | 89970 |
| rs141770617 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239383 | ATGTAAATGACAGCG[C/T]TTCTGGGTTATGCAT | 89970 |
| rs141839474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195782 | AATCCCAGCACTTTG[A/G]GAGGCTGAAGTGGGT | 89970 |
| rs141933847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187461 | TATCGACTGAGTAGA[A/G]TCCCGCAGTTTTCCA | 89970 |
| rs141936673 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230555 | ATATTGGTGTATAGG[G/T]GTCAGATCAGTTACA | 89970 |
| rs141956532 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223675 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATTGCTG | 89970 |
| rs141968924 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191538 | GTATTCAGGAAGTAT[A/G]CTTAGTTTGGGGTGC | 89970 |
| rs141993888 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226313 | GGGTTTTTGGACCTC[A/G]CGCAAGAAAGAATTT | 89970 |
| rs142052846 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197171 | TTGTCTAAAGTGTAA[C/T]TGATTAGCTTTCACC | 89970 |
| rs142159365 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203255 | GAGCTAAGATCATAC[C/G]ACTGCACTCCAGCCT | 89970 |
| rs142331358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207862 | TGGGTCATTGTGGAC[A/G]GTGACTGGAAATGAG | 89970 |
| rs142341064 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239153 | TTAGAATCTAATCCA[A/G]CTTGCCAGCCCTGAG | 89970 |
| rs142482039 | snp | A/G | 0.168135 | 0.236216 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212745 | TAAGCCTCCTGAGTA[A/G]CTGGGATTACAGGCG | 89970 |
| rs142504176 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235419 | CTGTTTTGTTTACTC[A/C]GTACTGTATTTTTGA | 89970 |
| rs142514417 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222940 | TCGATGAAATTATAA[C/T]TTTTGCCATGTAGTT | 89970 |
| rs142613052 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184922 | GTCGGCTCAATACTT[-/TG]TATCAAAAAGGAGTC | 89970 |
| rs142744247 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224960 | CTTTTACTTATGCCA[C/T]AATGCCTACATTTTA | 89970 |
| rs142773510 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234637 | TGCTTCCATTCCATG[A/C]TGAGTGAAAGTATAA | 89970 |
| rs142781787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228512 | TTTTAAAGGATTATT[C/T]GAGTAATATGTTTAT | 89970 |
| rs142793415 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219361 | TGCCATTTTTACTGG[A/G]GTGAGATGATAGCTC | 89970 |
| rs142839554 | snp | C/G/T | 0.000762226 | 0.0195075 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57230772 | CTTCTTTTTAAATGG[C/G/T]AACCAGCTGCCTCCT | 89970 |
| rs142859007 | in-del | -/CTACATTACCCAAGCTGGTCTCAGCCTCCTGGGCTCAAGCAATC | 0.227074 | 0.248947 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197924 | AGAAATGGGGTCTTG[lengthTooLong]CTCCCAACTCAGCCT | 89970 |
| rs142933848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187850 | CTTTTGCTCTCAGAG[G/T]TTTCATTTACTTTGA | 89970 |
| rs143134151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189891 | CCACCATGCCTGGCC[C/T]CGTGAGCTTAATTTA | 89970 |
| rs143190122 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236830 | GACCTAGCAACGCAA[C/G]TGGCAGGGGGAGTTA | 89970 |
| rs143221323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198615 | ATTCTTTTTGCTTTT[C/T]TTTCCCCCTGAAATT | 89970 |
| rs143229039 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195914 | GTAGTCCTGGCTACT[C/T]GGGAGGCTGAGGTAG | 89970 |
| rs143265352 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185873 | GGCGCCCACCCCAAA[-/C]CCGCCACCGCAGAGC | 89970 |
| rs143267902 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199258 | CCAGCACTTTGGTAG[G/T]CCGAGGCGGGCGGAT | 89970 |
| rs143327224 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205546 | CTGCAAGGCACACCT[A/G]TACCTGTTTTGTCTT | 89970 |
| rs143383585 | snp | A/G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235747 | CAGTCAATGTGTGCC[A/G/T]ATTGTTTATGAGCAA | 89970 |
| rs143480956 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196710 | ACGGGGTAGTTCTGT[A/G]AAAGATAAATTCTTT | 89970 |
| rs143528824 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237671 | CAGCCAAATGCTAGT[A/G]TCTCTTTATTTTTTT | 89970 |
| rs143556344 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226739 | ATCCTGTTTTATCAG[C/T]AGGGTCTTTGTGACC | 89970 |
| rs143618678 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214218 | ATGATTGGCTCTTTT[A/G]CATGTTCCTTGAGTT | 89970 |
| rs143640298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236252 | GATCTGGTCTTAATC[A/C]TCTTTGAGCTCTCTG | 89970 |
| rs143649062 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214750 | AGACTAAATGAGGGC[C/T]GGGCACGGTGGCTCA | 89970 |
| rs143659860 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195374 | AAAATGAGCCAGGCG[C/T]GGTGGCAGGCACCTG | 89970 |
| rs143686423 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218560 | AGTTGTTTTTAGCTC[A/C]CACAAAAATTAGTGA | 89970 |
| rs143749579 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239482 | AAAATTAGAATCACA[C/T]AGTCAGTACTACAAG | 89970 |
| rs143934894 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215055 | AGACTAAATGAGAAG[A/G]TGGGTGGTATGGGTA | 89970 |
| rs144055620 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236359 | AGTATGATCATAGTC[C/T]CCATAGTAGATATAT | 89970 |
| rs144078768 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237961 | GCATTTCAAGAGATG[C/T]TGGGAATAAGATAAG | 89970 |
| rs144097835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197352 | AGCCCTCAAGAGTAC[G/T]CTGTGTAGTCATCTC | 89970 |
| rs144163670 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226375 | AAGTTTATTAAAGAA[A/G]CAGAAGAATGGCTAC | 89970 |
| rs144169830 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202243 | ACGGGGGGTGGGTGG[C/T]GGGGGTCCTTGTTCT | 89970 |
| rs144205967 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230904 | GTCCATTTATATATG[C/T]AATTGTGATGAGAAA | 89970 |
| rs144303050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219428 | AATGTTGAGTACCTT[C/T]TCATATATCTGTTTG | 89970 |
| rs144350677 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188758 | CGACGTCCTGTAATC[A/C]GCCTGCCTCGGCCTC | 89970 |
| rs144385765 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192798 | GCAGCCTCGACCTCC[C/T]CAGCTCAGGCGATCC | 89970 |
| rs144403290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217463 | AGTCATGTCTTACCT[A/G]CATCATGAGAATTGT | 89970 |
| rs144555215 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222095 | CAGGAATATTTTGTT[G/T]TCATATGGTTTCTAC | 89970 |
| rs144611114 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213458 | TATAAAGTTTAGCTC[A/G]ATTATGAAGACATAC | 89970 |
| rs144724351 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217791 | CTCACTCCCCCATCC[A/G]TGGTTAATACTACGC | 89970 |
| rs144729278 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224278 | GTTTGATGGGAAGGT[C/T]CAGCTGGCCAAGCCT | 89970 |
| rs144743054 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232532 | ACCTCTCCCTTATCT[A/G]TCATACCCCGTTCTT | 89970 |
| rs145012499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189175 | AATTTTTGTATTTTT[A/G]GTAGAGAGGGAGTTT | 89970 |
| rs145048353 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232918 | TAGTTGTCAGGAGCC[A/T]AACTGAGTGGCCACC | 89970 |
| rs145052084 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193477 | AGATTGTGGTCTTTG[A/G]GGTGTTCTGCAGGCT | 89970 |
| rs145068083 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236068 | ACAGTGATTCCAGCT[C/G]TGATTAATCCTCCCT | 89970 |
| rs145069099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190853 | TAAAAGTAGTAACTT[C/T]AGATAAATGTGTGGT | 89970 |
| rs145108388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189367 | GGGCTTCTGCTTTTG[C/T]CAGCAAAATAACTTT | 89970 |
| rs145153514 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212637 | CCCACCCCCCTGAGA[C/T]GGAGCCTTGCTCTGT | 89970 |
| rs145217389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211437 | TAGCCAGCACGATGG[C/T]GTGCACCTGTAATCC | 89970 |
| rs145217551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238699 | CCACAGACTAAGACA[A/G]TTGAGGATCAGAAAT | 89970 |
| rs145237343 | snp | A/G | 0.16846 | 0.236329 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198371 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 89970 |
| rs145330508 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209583 | TGGCCAGGCTGGTCT[G/T]GAACTCCTGACCTCA | 89970 |
| rs145350138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212509 | AATCTAGTAAGTCAT[A/G]TAAGGAGACTTTCAG | 89970 |
| rs145413165 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194618 | ACTATTTTGGAATGA[A/T]AAGGTGAAGATTATA | 89970 |
| rs145523580 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222343 | AAGCCATCCTCTTAC[C/G]TCAGCCTCCTGAATA | 89970 |
| rs145606409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194188 | AGTATACTGATGCCT[A/G]TAGTTTACTTTGAAA | 89970 |
| rs145681576 | in-del | -/T | 0.17138 | 0.237316 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222137 | GAAAAGCCCCTTGGA[-/T]TTATTTTGTTAATCT | 89970 |
| rs145688335 | snp | C/T | 0.00118847 | 0.024348 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57213085 | CCTAGGCTGCTTGGC[C/T]GAGAAACTAGCAGGT | 89970 |
| rs145723767 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228168 | GTCCCGGCTACTTGG[G/T]AGGCTGAGGCAGGAG | 89970 |
| rs145752859 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236109 | CAGCCCAGAATTTCT[A/C]AGTTTGAGCATATTT | 89970 |
| rs145760573 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212860 | CCTTGTGGTCCGCCC[A/G]CCTCGGCCTCCCAAA | 89970 |
| rs145769376 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184558 | AAAGGTGACTAATGG[C/T]GAACACGTTGAAAAT | 89970 |
| rs145874719 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215606 | CTGTCTACCATCAGC[A/T]TTTGTAGAATTCCTT | 89970 |
| rs145931473 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211007 | TGGTTAAAAAAAGAA[A/G]TATTTGTATCTCAGG | 89970 |
| rs146088516 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187028 | CGGAATGTCCTACTA[C/T]GGAAGCCGGAGCTGA | 89970 |
| rs146132626 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218621 | ACTTATTTCACTTAA[C/T]ATCATATCCTACAGT | 89970 |
| rs146163790 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225138 | TGATCTCTGCTCACT[A/G]CAACCTCTGCCTCCC | 89970 |
| rs146210123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206624 | CTGGCGTACAGTGGC[A/G]TGATCATGACTCACT | 89970 |
| rs146214310 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223677 | CTCGGGAGGCTGAGG[C/T]AGGAGAATTGCTGGA | 89970 |
| rs146265370 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237735 | TTTATTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 89970 |
| rs146293193 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191654 | CAATTTAATTTATAG[A/G]TTTTTTTGTTTACTT | 89970 |
| rs146402880 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187522 | GTGGAGTGACTTAAC[C/T]TCCTTAAGTCTCTAC | 89970 |
| rs146460263 | snp | G/T | 0.0269296 | 0.11287 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213128 | CTCCACAGTGGAAGA[G/T]CTTAAGTTGTTTGAC | 89970 |
| rs146474141 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197630 | TCTTTTGGAAGAAAC[G/T]GACTCAAAACACACT | 89970 |
| rs146516531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202439 | CAGGGACCCTTTAAA[G/T]AATTATTCCTATTTC | 89970 |
| rs146577529 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232711 | TTAAACCTTCCCAAA[A/C/T]TCAGATGGCAATGGG | 89970 |
| rs146595587 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217591 | GACTGAAAGTATTTC[A/G]GATTTCACATTTTTT | 89970 |
| rs146737615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235750 | TCAATGTGTGCCGAT[C/T]GTTTATGAGCAACAC | 89970 |
| rs146822629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194668 | CAAAGTCTGGTTTTT[A/C]TTCTTTATGGTCACT | 89970 |
| rs146849995 | snp | A/C | 6.59554e-05 | 0.00574224 | missense | RSPRY1 | GRCh38.p7 | 16:57209079 | TTTGCTCTTAGATGA[A/C]GGATGGTTGGATGTT | 89970 |
| rs146901651 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236382 | AGATATATATCCAAA[A/G]TAGAGTTGGAAGAGG | 89970 |
| rs146912143 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239216 | GCTAGCAGCCAGGCC[G/T]GTGGTACTTCCATGA | 89970 |
| rs147023223 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185238 | TACGAACAAACAGGT[A/C]TCCCCCTTTCCTCTG | 89970 |
| rs147084939 | in-del | -/TT | 0.00835141 | 0.0640778 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191602 | TCATCATGATTCCTC[-/TT]TTTTTATTAGAATTT | 89970 |
| rs147121129 | snp | C/T | 0.00225442 | 0.0334982 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204847 | CCAACAGCAACAGGC[C/T]GAGAACAGTGCAGTA | 89970 |
| rs147170415 | snp | A/G/T | 0.00875054 | 0.0656008 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230556 | TATTGGTGTATAGGG[A/G/T]TCAGATCAGTTACAG | 89970 |
| rs147286854 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234117 | CCTATTTCCTACCCT[C/T]TCCCGTTTTCTCATG | 89970 |
| rs147377862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234650 | TGCTGAGTGAAAGTA[C/T]AATGGAAGGGTTCTA | 89970 |
| rs147388295 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193397 | GCAAGTGTAATCTTC[A/G]TGCATTACCAAATCA | 89970 |
| rs147486977 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211956 | GGGAAAGTCTTTAGC[A/G]TAGTCACCAATGAAT | 89970 |
| rs147502260 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195932 | GAGGCTGAGGTAGGC[A/G]AATCACTTGAACCCA | 89970 |
| rs147573040 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223252 | ATTCCTAGGATACAC[C/G]CAGTTTCAAAAGATT | 89970 |
| rs147750302 | snp | C/G | 0.168135 | 0.236216 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209594 | GTCTTGAACTCCTGA[C/G]CTCAGGTGATCCACC | 89970 |
| rs147761427 | snp | C/G | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184901 | TAAAAGACTGTAAAA[C/G]CTGCTGTCGGCTCAA | 89970 |
| rs147856446 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226410 | TAGGCAGAGCAGTGG[C/T]GTGGGCTGCTCAACT | 89970 |
| rs147866214 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203888 | CAAAGCCTTGCTTAC[A/G]TAACAGAAACACTTT | 89970 |
| rs147902966 | snp | A/T | 0.00175094 | 0.0295365 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209057 | CTCCATCATATAATC[A/T]TCTTGATTTGCTCTT | 89970 |
| rs148009039 | snp | A/G | 0.0143105 | 0.0833695 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239613 | TTTTTTGTTTTTTGG[A/G]TTTTTTTTTTTTACT | 89970 |
| rs148044843 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227124 | TGCCTGAACAAAGGA[A/G]GCACTGGGAAAATAT | 89970 |
| rs148050913 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214465 | TGGCCTGTGGTCTTG[A/G]ATGGTCTGTATTTTT | 89970 |
| rs148055391 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185394 | AGCAACTGGTACATG[A/G]CACACAATAAATGTG | 89970 |
| rs148079684 | in-del | -/TTTTG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208181 | TAGCCACCTTTTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 89970 |
| rs148168064 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236355 | CTTAAGTATGATCAT[A/T]GTCTCCATAGTAGAT | 89970 |
| rs148220314 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205845 | TAATGTACATAAGGC[A/C]TTCAGTGTGGAGCTT | 89970 |
| rs148274544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211026 | TTGTATCTCAGGTGG[C/T]GATCTTTATTCAGAA | 89970 |
| rs148310551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232987 | CATTCCAGTTGTGCT[C/T]AATTATAAATTGTGG | 89970 |
| rs148410962 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234854 | TGGACTTAGAACTAA[A/G]GGATTTTAATTTGAT | 89970 |
| rs148426740 | in-del | -/G | 0.02016 | 0.0983543 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214535 | TCAAAACTCTGGTCT[-/G]AAAACCCTTATTTGT | 89970 |
| rs148567283 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229963 | GCCCACCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 89970 |
| rs148576370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187675 | GTAAAGTAGTATGTA[A/G]AGGTAAGGGGTGGGA | 89970 |
| rs148608815 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237332 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 89970 |
| rs148618887 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196823 | GCTCATTTTGTAACA[C/G/T]CTTGCATTTTTTTGA | 89970 |
| rs148714622 | snp | A/G/T | 0.0138799 | 0.0821421 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212684 | CAGTGGCACGATCTC[A/G/T]GCTCACTGCAACCTC | 89970 |
| rs148735024 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220249 | AGATTGCTTTGAGTA[A/G]TATGGACATTTTAAC | 89970 |
| rs148746469 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208655 | TCCTCCTGCCTCAGC[C/G]TCCCAAAGTGCTGGG | 89970 |
| rs148783556 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192990 | CAGAGTGTTGGGATT[A/G]CAGGTGTGAGCCACC | 89970 |
| rs148837605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222799 | GGGATTCTTCCAGGG[A/G]GGAAGCTTCGATATA | 89970 |
| rs148891084 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226666 | GACCAGAGGTCACTT[C/T]TGTTGCCATCTTGGT | 89970 |
| rs148932706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236138 | TTGGAGGGTTTAGTT[A/G]TCAGGGCCTCACAGA | 89970 |
| rs149095201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232516 | CAAAGTCTGAGGGGA[C/T]ACCTCTCCCTTATCT | 89970 |
| rs149104747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189816 | GGCTGGTCTCAAACT[A/C]CTGGGCACAAGCCAT | 89970 |
| rs149148176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198490 | ATTTAAGATCCAACA[A/G]ACCTCTTTTTAACTT | 89970 |
| rs149195635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205527 | GGAAGCTTGTCAGTT[C/G]ATACTGCAAGGCACA | 89970 |
| rs149245211 | in-del | -/ATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208398 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 89970 |
| rs149366386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224231 | CCATCCTAACTATCC[C/T]TCTGTTTGGGGTCAC | 89970 |
| rs149541223 | snp | A/G | 3.30808e-05 | 0.00406686 | missense | RSPRY1 | GRCh38.p7 | 16:57227397 | ATGATGGCTGCCGGC[A/G]GCTGATTTGGTACAA | 89970 |
| rs149620070 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234014 | GTGCGTGGCTTCTTA[C/T]TCACTGAACGGAAAA | 89970 |
| rs149629508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192515 | CTATTATTTGCTTCC[A/G]GAAATTCCTTACTCT | 89970 |
| rs149757587 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194105 | CAGTGTATGTAAATT[C/T]GACTCCTAAAAACTT | 89970 |
| rs149768165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215541 | CTTAAAGGGGAACTC[A/G]TGTGACATGAGCTTA | 89970 |
| rs149772885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203727 | TTCTCCTAGTCCAGC[A/G]TGGTACCTGGCACAA | 89970 |
| rs149821351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222308 | TGTGTTGCTCAGGCT[A/G]GCCTCAAACTCCTGG | 89970 |
| rs149867827 | in-del | -/CACACACA | 0.189576 | 0.242588 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240340 | AGTCTTCCATAAATC[-/CACACACA]CACACACACACAAAA | 89970 |
| rs149889245 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204806 | ATCTGCCGAGATGAC[A/G]GTGGAACAGATGACA | 89970 |
| rs149917070 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226166 | AGCTGAGTGTCCACT[A/C]TAACCTTTCTCTTAT | 89970 |
| rs149970301 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231830 | GCAAAGATGACAACA[C/G]TGTTCCACAACCATC | 89970 |
| rs149986174 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238551 | AGATGGACTGTTTGG[A/T]AAATGATTCTGGGAT | 89970 |
| rs150131565 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185867 | CCTCGGCGGCGCCCA[C/G]CCCAAACCGCCACCG | 89970 |
| rs150201254 | snp | C/T | 0.000148262 | 0.00860865 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57221367 | AGTGGTCACTTCTGG[C/T]GTCATGCAGATTGGC | 89970 |
| rs150247541 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209988 | GCCACATTCTCTATC[A/G]AGGCTTTATTTAATT | 89970 |
| rs150289112 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218352 | ATTTCTTTGTTTTGC[A/G]CTTTTCTTTTAGTTA | 89970 |
| rs150342834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224079 | ATTTAGAAGCCTTTC[C/T]GGAGCCTCCAGATTA | 89970 |
| rs150442259 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198110 | TACTAAATGGGCCGG[A/G]CACGGTGGCTCACAC | 89970 |
| rs150492062 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233379 | TGTTTTTTTAATTTT[A/T]ATTTTTTATTTTTTG | 89970 |
| rs150534880 | snp | A/T | 0.00953873 | 0.0683987 | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240679 | ATGCTTGTAGAGCTT[A/T]TGTCTAATAAGCTTG | 89970 |
| rs150639937 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215466 | CTCTGGTGGCTCCCA[A/G]TGTAGCAGTAGGGAA | 89970 |
| rs150654536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188098 | CTCCACGAATACTAT[A/G]CGTTGTTGTGGTAGC | 89970 |
| rs150796157 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211155 | AAAACTGGGCTGAAT[A/G]TACTGGCTCATGCCT | 89970 |
| rs150812338 | snp | A/G | 0.000232107 | 0.0107703 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221452 | GAAAATGGGAGCAGT[A/G]GCAGTTTGCTTTTTC | 89970 |
| rs150866412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225537 | AGAACTTTTTTTCCA[A/C]TCTCTCTCCTCACTG | 89970 |
| rs150919285 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193654 | CACGCCACTGTGCCT[A/G]GCTAATTTTTGTATT | 89970 |
| rs151014640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235483 | AATGCTATTTATGAG[C/T]TTCCTAGGCACTCTT | 89970 |
| rs151068104 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203460 | ACACTAGCATAGTCT[A/G]TTCCTTATGTGGCCT | 89970 |
| rs151164188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217834 | GGACATGTAAATCCA[C/T]CCCCACTGTTACCCC | 89970 |
| rs151226104 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197185 | ATTGATTAGCTTTCA[C/T]CCAGTCTTTTGCCTG | 89970 |
| rs151273521 | in-del | -/AGTA | 0.00755907 | 0.0610114 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187022 | ACTAGCGGAATGTCC[-/AGTA]TACTACGGAAGCCGG | 89970 |
| rs151279718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238138 | AGCAAGAAATATGTA[A/G]AGCGTATATGAAGAA | 89970 |
| rs151320039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212834 | TGGCCAGGCTGGTGT[C/T]GAACTCTTGACCTTG | 89970 |
| rs180675440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187533 | TAACCTCCTTAAGTC[C/T]CTACTGTAAAATAAC | 89970 |
| rs180692104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236353 | ATCTTAAGTATGATC[A/G]TAGTCTCCATAGTAG | 89970 |
| rs180700504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199276 | GAGGCGGGCGGATCA[C/T]GAAGTCAAGAGTTTG | 89970 |
| rs180707980 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225562 | TCACTGTATTGTTTG[C/T]CCCATAGAAGAAGCA | 89970 |
| rs180887718 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193295 | CTACCCCCTTCTTAC[C/G]TTCCCCAATGAAATA | 89970 |
| rs180923403 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221743 | TTATACAGGAAGTAG[A/T]GCTGATTATTACCTT | 89970 |
| rs180996273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232803 | TATATAAATTTGGTA[C/T]CCAAAGTTCGTCTTG | 89970 |
| rs181021260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207849 | CCCATTTTGTCTGTG[C/G]GTCATTGTGGACAGT | 89970 |
| rs181185407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193793 | CATTTCAGCCGGGTG[C/T]GGTGGCTCACGCCTG | 89970 |
| rs181192688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222207 | TGGGTTTTAGAAGTG[A/G]TCCAACAAAATCAAG | 89970 |
| rs181475851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206975 | TACAACTGCTTCTGA[C/G]TATTACAGAGTATTC | 89970 |
| rs181486762 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193911 | TCTCTACTGAAAACA[C/G]AAACATTAGCTGGGT | 89970 |
| rs181622143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222685 | CTTCCTATTCTACAA[C/G]AGTTGTTTTCTTTGT | 89970 |
| rs181655821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215107 | AAGTCAGACTTCCTG[A/G]TGAAGGTGGACCCTC | 89970 |
| rs181659269 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237234 | CTGCAGCCTCTGCCT[C/T]CTGGGTTCATGCAAT | 89970 |
| rs181852674 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226806 | TAAGAATGCCTAACC[G/T]CTTGGGAATGCAGCT | 89970 |
| rs181892237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227162 | TGAAGTCATTATCTA[C/T]TCACTTGGAACCAGC | 89970 |
| rs181922697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202146 | GGGAACATAGCAAGA[C/T]CCCATCTCTAAAAAA | 89970 |
| rs182042430 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200417 | TTCTCAATGAGCTGT[G/T]GAGTACATCTCCCAG | 89970 |
| rs182088933 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214393 | CTGGAATATTTAATA[C/T]ATTGTCTATGAAGCT | 89970 |
| rs182135072 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218421 | CCCTGTTATGCTGTC[A/C]AATACTAGGTGTTCT | 89970 |
| rs182164199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227752 | TTTTGAATTAAAGCA[G/T]CCATGGCAATATCAG | 89970 |
| rs182165496 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189823 | CTCAAACTCCTGGGC[A/T]CAAGCCATCCACCCA | 89970 |
| rs182303558 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186896 | GACGCTTTAGGAGGG[C/T]TCTTTTTGTGGAGTT | 89970 |
| rs182382189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222810 | AGGGAGGAAGCTTCG[A/G]TATAAAACTTGTCTC | 89970 |
| rs182389757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235995 | TGTGCACTTAAGGGA[A/G]GTAGAGTGTGTCTCA | 89970 |
| rs182426878 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194910 | GTGTTTTATAAAGAC[A/G]GTGAGTACCAGAACC | 89970 |
| rs182433621 | snp | G/T | 5.01802e-05 | 0.00500875 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238989 | GACACATGTGAAGAG[G/T]CATCGTGGACTTTTT | 89970 |
| rs182449629 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203516 | TTTGTTTGTTTGTTT[G/T]TTTACTTTTTGCTAC | 89970 |
| rs182654235 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196213 | TATGGAGCCATTTTT[C/T]CCTTTGTGTTGATAT | 89970 |
| rs182675950 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184564 | GACTAATGGTGAACA[C/T]GTTGAAAATGCTTAA | 89970 |
| rs182706293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224229 | ATCCATCCTAACTAT[C/T]CCTCTGTTTGGGGTC | 89970 |
| rs182743887 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234625 | GTTTTGCCTGTCTGC[A/T]TCCATTCCATGCTGA | 89970 |
| rs182787828 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211281 | TAAAAAAAAAAAAAA[A/G]AAAGAAAGCCAGGCA | 89970 |
| rs182794209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234105 | TTACTTTTCTGACCT[A/G]TTTCCTACCCTCTCC | 89970 |
| rs182960008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210429 | CATTTAAGGCTGGGC[A/G]CGGTGGTTCACGCCT | 89970 |
| rs182964210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212547 | AGATATTTCCCATCA[A/G]TGATATCATTAGGGT | 89970 |
| rs183000600 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188354 | ATTTCCTGGGATGGT[A/G]TCTTGCTTTGTAGAT | 89970 |
| rs183240437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233566 | GTAGAGACTGGGTTT[C/T]GCCATGTTGCCCAGG | 89970 |
| rs183271541 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204420 | ATTAGAATCCTAATA[G/T]CTATAAAATCAGACT | 89970 |
| rs183281531 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229768 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 89970 |
| rs183556415 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229080 | CCTCATTGTTGGACA[A/C]TGACATTTTTGCCTT | 89970 |
| rs183575595 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193539 | GCTCTGTCACCCAGG[A/C]TTGAGGGTAGTGGGA | 89970 |
| rs183577140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222083 | TCCAGTTTTGATCAG[A/G]AATATTTTGTTTTCA | 89970 |
| rs183777658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203960 | CCAATGGGAAACTCT[A/C]TCCTTTTATTCTCCT | 89970 |
| rs183793138 | snp | C/T | 0 | 0 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198567 | AAATACTTTTATGTG[C/T]TGGCATTAAATTGTA | 89970 |
| rs183796137 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225218 | GGTGTGCGCCACCAC[A/T]CCTGGATAATTTTTG | 89970 |
| rs183836272 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216515 | TTCAGGCCAGGAATT[A/C]GAGACCAGGGTGGGC | 89970 |
| rs184013832 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189090 | CCTCTGCCTCCCGGG[G/T]TCAAGCAATTCTTCT | 89970 |
| rs184077533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238496 | ACTAAAAATGAAAAT[G/T]TACCATATGACAAAG | 89970 |
| rs184168169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206160 | GTAATTCCAACACTT[C/T]TGAGAGGCTGAGGTA | 89970 |
| rs184215178 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185470 | AGACGCCGCACATCC[C/G]AGTGAGTAACCTGGA | 89970 |
| rs184323418 | snp | C/T | 0.000178785 | 0.00945308 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230853 | ATTCGAGTAGATGCA[C/T]GGAATGCCCTTTTCT | 89970 |
| rs184410912 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186276 | TGCCACCGAGGAAGG[A/G]GCGTTTCCTAGGGGA | 89970 |
| rs184466087 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213949 | GCTACAGTGTCTGGT[A/G]AGTGAGACATCAAAA | 89970 |
| rs184470732 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235815 | CATCATATCCCATAC[C/G]CTGCCTTGGTCTTAT | 89970 |
| rs184517480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236106 | CTACAGCCCAGAATT[G/T]CTCAGTTTGAGCATA | 89970 |
| rs184654175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190483 | GGAAACACAGTGGAA[A/C]CAGCAATCTATTTCA | 89970 |
| rs184706498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219759 | TGGAGAGTTTCCCCA[A/G]TGTTTTATTTTAGTA | 89970 |
| rs184716141 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239824 | TTTTTGTTAAAAAAA[A/T]TTTTTTTAATCAGTA | 89970 |
| rs184793035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225693 | TGCATGCTGCTTCTA[C/T]TTTTTATAAGCACTC | 89970 |
| rs184893568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235343 | GGAACTAGAGTTTAA[A/G]TAGAACCTGGCTGTC | 89970 |
| rs184900122 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199318 | ACCAACATGGTGAAG[A/T]TCTGTCTCTACTAAA | 89970 |
| rs185025571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196699 | ATTACTTCAGTACGG[A/G]GTAGTTCTGTAAAAG | 89970 |
| rs185148487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224590 | AGCCAATGGAAACCA[A/G]AATTAATCCTGCTGG | 89970 |
| rs185302389 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210577 | AAATCAGCCGGGAGT[A/G]GTGGCAGGCACCTGT | 89970 |
| rs185323931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231619 | CAAACCCAGAAAGAC[A/G]GAACACTTTCAAATT | 89970 |
| rs185480739 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202959 | CTATGTTTTCCCTGT[A/G]GCAGTAATCAAACTG | 89970 |
| rs185486301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206509 | AAACAATGTTAATTT[A/C]AGCTCATTGGAAAAA | 89970 |
| rs185546909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187739 | CTGGGAGCCATATTG[C/T]ACTGAAAGCTTCAAG | 89970 |
| rs185561350 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214731 | GGGAGAAAGTACTTC[A/G]TCAAGACTAAATGAG | 89970 |
| rs185566121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220269 | GACATTTTAACAATA[C/T]TGAGTCTTCCAATCC | 89970 |
| rs185567719 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236854 | GGAGTTATCTTAGGA[A/G]TGCAAGGATGGTACA | 89970 |
| rs185692039 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192763 | TAGGCTGAAGTGCAG[C/T]GGTGCGATCATGGTT | 89970 |
| rs185706377 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240416 | TCTCTTCTTTAGCTT[A/G]TGGTGAATACAGTAA | 89970 |
| rs185786214 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215355 | AATAGAATGCTGAAT[A/G]GGCTTTCCAGCAGCA | 89970 |
| rs185843195 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237628 | ATGGATGGATACTTC[C/T]ATAACAATACAAAAA | 89970 |
| rs185857830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207982 | CTTTTTACCTCCACA[C/T]CTCCAGTTTGAATTC | 89970 |
| rs185997259 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233192 | GTGTTGTATATACTC[G/T]CTGTCTGTAATTCTT | 89970 |
| rs186032408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222527 | TGGAGAGGTCAAGTC[G/T]GTACTCCTGTCTGGG | 89970 |
| rs186148381 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186946 | ATGAGGCATACCTCC[C/T]CGGGGAGATTTAGAA | 89970 |
| rs186198571 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233791 | ATCCAGTAGGCTGTG[C/G]CTTCAGAATATATCC | 89970 |
| rs186242209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214423 | TTCTGGTTTGCTGAG[G/T]CTGTGCCCTCAGATC | 89970 |
| rs186301257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227213 | TATTTTCAAAAAACC[A/G]TGAGCTCTCTCATCA | 89970 |
| rs186403851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228446 | TTCATTTAATGGAGC[A/G]TATGATAAAGGCCCT | 89970 |
| rs186499384 | snp | A/G | 0.000185374 | 0.00962562 | intron-variant, missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57207651 | CATAAGTCCTCAACC[A/G]GGATTGTCGTCTCTC | 89970 |
| rs186505791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232400 | GAACATAAGGGTTGC[A/G]TATGTTCCCGCTCAG | 89970 |
| rs186609150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203543 | CTACCAGCCCATGTA[A/G]GTCTCCTATTTCTAA | 89970 |
| rs186719674 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195217 | CAAAATTGTTATCGA[A/G]AGTATAATATTAGGC | 89970 |
| rs186775832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223204 | TGAATCTTTTTGCCT[A/G]TTCAGACAGGGTGTG | 89970 |
| rs186868064 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226915 | CAATCTTGTGCTGAT[A/T]TACAAGTGTACTGAC | 89970 |
| rs186877372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188618 | GCCTCCTGGGTTCAA[C/G]CGATTCTCCTGCCTC | 89970 |
| rs186937599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193794 | ATTTCAGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 89970 |
| rs187235087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189935 | TGTATATGCTTTCCT[G/T]AACAATGAAGTAATT | 89970 |
| rs187290672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218574 | CCCACAAAAATTAGT[G/T]AGAACACACGAAGTT | 89970 |
| rs187302599 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239163 | ATCCAACTTGCCAGC[C/G]CTGAGAAAATCCCTT | 89970 |
| rs187310933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222720 | AAAAATGGGGAAAAT[A/C]TCAGAGAATTAGCTA | 89970 |
| rs187355674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204013 | ATTTGTATCATAACT[C/T]TTTTTTAACAACAAA | 89970 |
| rs187493141 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239825 | TTTTGTTAAAAAAAA[A/T]TTTTTTAATCAGTAT | 89970 |
| rs187550501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205540 | TTGATACTGCAAGGC[A/T]CACCTGTACCTGTTT | 89970 |
| rs187553509 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229908 | GATGGGGTTTCACCA[A/T]GTTGGCTGTGCTGGT | 89970 |
| rs187565351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194251 | ATAAGAGATGGATAG[C/G]GATAAAGCAAGTTTA | 89970 |
| rs187591372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212688 | GGCACGATCTCGGCT[C/T]ACTGCAACCTCTACC | 89970 |
| rs187788628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196532 | GCATCCCAGAAATTC[C/T]GATTCTGGCTATTCG | 89970 |
| rs187822513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211494 | GAATCACTTGAACTC[A/G]GAAGGTGGAGGCTGC | 89970 |
| rs187823194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234673 | GGGTTCTAACTTGAG[A/G]TGTTTGGACTTGCAG | 89970 |
| rs187826573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234218 | GCTGTTCCTGCTACC[C/T]GAAACGGTTTCTCCA | 89970 |
| rs187851278 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184618 | TACACTATGACTGAC[A/C]CTGTACGTACATCGC | 89970 |
| rs188076219 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224512 | AAAATATGCATGACC[A/G]AAAAACAGGTAGTTC | 89970 |
| rs188111989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199221 | AAAAAGCGGCTGGGC[A/G]CGGCGGTTGATGCCT | 89970 |
| rs188124476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225553 | TCTCTCTCCTCACTG[A/T]ATTGTTTGCCCCATA | 89970 |
| rs188335953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220009 | TTCTGTTCCATTGGT[A/C]CATGTGTCTGTTTTT | 89970 |
| rs188492924 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185520 | AACGGAGCCTGCTAC[C/T]CACTTGAAACCTGGG | 89970 |
| rs188502689 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213196 | CTGCTATACCAGAAA[G/T]AAATCTCTTAAAAAT | 89970 |
| rs188562003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235625 | AGCCTGGACCCTATA[G/T]AACAGAGTGAGCATC | 89970 |
| rs188581335 | snp | A/G | 0.000467625 | 0.0152838 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238842 | GTTTGACCTTTTGAA[A/G]CATTAACTTGACTGA | 89970 |
| rs188618463 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189194 | GAGAGGGAGTTTCAC[C/T]GTGTTGGTCAGGCTG | 89970 |
| rs188654116 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229327 | CAAAATTGGGCCAGA[C/T]GTGGTGGCTCATACT | 89970 |
| rs188654275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190517 | GAATTATTTGGGGAT[A/G]ATAAACTATGGATTT | 89970 |
| rs188654921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193755 | TGATAAAACTCAGCA[C/T]GTTACTGTGCTTAAG | 89970 |
| rs188660913 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222091 | TGATCAGGAATATTT[C/T]GTTTTCATATGGTTT | 89970 |
| rs188904325 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216728 | CTGTGACTAAAAAAA[A/C]GGAAAACAAAATAGT | 89970 |
| rs188914683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224907 | TGTCAAGGACTTCTC[A/G]GGACATTAGAAGGTG | 89970 |
| rs189042822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206935 | CTTTTCTCAACATCG[A/G]AATCTGTGTTACTGT | 89970 |
| rs189105857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232168 | CATGACATAGCTAAT[A/G]TCGGACTGGTATGCC | 89970 |
| rs189184628 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197690 | TTGTCTTCTTACCTT[C/G]GTATTTAGTCAGTTT | 89970 |
| rs189324955 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207782 | TGATCTCCAGTTTTA[C/T]TCCTGTGCTTTTACC | 89970 |
| rs189329022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232625 | AAAAGGGACAATTGA[C/T]CCATCTAAGTTCCCA | 89970 |
| rs189464909 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199458 | GATCGTACCATTGCA[C/T]TCCAGCCTGGGTGAC | 89970 |
| rs189485104 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187224 | CGGGCTTATTGCCCG[A/C]GTGGGGTGGGGAGAG | 89970 |
| rs189499312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236172 | ATGCAGAGTTTAAAG[A/G]TTGGATATCTTCATG | 89970 |
| rs189568218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214280 | AAACAATTACATGGC[A/G]TTCCAAGCCAGGAGG | 89970 |
| rs189579020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235852 | CATAGCTTTAGTCAC[A/G]TGGCTCCACAGGGGT | 89970 |
| rs189687783 | snp | A/G | 0.00382442 | 0.0435613 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230854 | TTCGAGTAGATGCAC[A/G]GAATGCCCTTTTCTC | 89970 |
| rs189743947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226748 | TATCAGCAGGGTCTT[C/T]GTGACCTGTATCTTG | 89970 |
| rs189893272 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203054 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 89970 |
| rs189962153 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57188219 | TGCATTTCCTGGGAT[A/G]GTATCTTGCTTTGTA | 89970 |
| rs189973251 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214860 | ATGGCGAAACCTGGT[C/G]CCTACTAAAAATACA | 89970 |
| rs189981468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236938 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACAAGGC | 89970 |
| rs189983845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206243 | ATCCCATCTCTGCAA[A/G]AAAAATTTAAAAATT | 89970 |
| rs190262629 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192866 | GACTATAGGGTCCAA[G/T]CCGCCACTCTGGCTA | 89970 |
| rs190283024 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240475 | CCTTTTTTGACTAAG[A/G]TTTCACAACTTTCAT | 89970 |
| rs190402424 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57223589 | GTTTGACTGGCCAAC[A/G]TGGTGAAACCCCGTC | 89970 |
| rs190436632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195328 | ACCAGCCTGGTGAAC[A/C]TGGTGAAACCCCATC | 89970 |
| rs190509992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210832 | AGACCAGCCTGGCAA[C/T]ATGGTGAAACCCTGT | 89970 |
| rs190519504 | snp | C/T | 0.000247066 | 0.0111118 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57221328 | CTTTTGTGTGGATGC[C/T]GGGGTATGGTACTAT | 89970 |
| rs190520236 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233944 | CAACACAGCCTCCAG[A/G]ATGATTTGTTACAAC | 89970 |
| rs190535582 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186724 | CCCTCTTTCGGGGGT[C/T]CTCACCAGAAGAGGT | 89970 |
| rs190565034 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227146 | GGAAAATATTTGTTG[G/T]TGAAGTCATTATCTA | 89970 |
| rs190803799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218005 | TAGCATTTGTTTGAT[C/T]GATCTTCAAATGGCA | 89970 |
| rs190899831 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194390 | CTAATTCAATTTTCT[G/T]TATGTTTGGAAAATT | 89970 |
| rs191037859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238143 | GAAATATGTAGAGCG[C/T]ATATGAAGAAAACTT | 89970 |
| rs191047491 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189788 | TTAAGACAGGGTTAC[A/G]CCATGTTGCCCAGGC | 89970 |
| rs191106175 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203845 | GTGAAAATACAACTT[C/T]TGTGATATCAGTTTT | 89970 |
| rs191113490 | snp | A/C | 0.000399281 | 0.0141238 | missense | RSPRY1 | GRCh38.p7 | 16:57238955 | GTATCTAGAATCAGA[A/C]AGATTTCTCATATTT | 89970 |
| rs191157569 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201894 | GGGAGTTTGCAGTGA[C/G]CCGAGATGGCAGCAG | 89970 |
| rs191364328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228486 | AACTAGCTTGTTTTT[C/T]AATAAGAATTTTTTA | 89970 |
| rs191372418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57205834 | TTATCATGAGATAAT[A/G]TACATAAGGCATTCA | 89970 |
| rs191373971 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233320 | TCTCAGCTACAAGTC[A/T]TCCACTCACAGCCAC | 89970 |
| rs191379093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230401 | AAGTGACCACATGAT[C/T]TTTTGATCTTACCAT | 89970 |
| rs191609629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208639 | TCCTGGGCTCAAGGG[A/G]TCCTCCTGCCTCAGC | 89970 |
| rs191626653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222602 | TAGCTTTTACTGTTA[C/T]AATTTCCATTTCACA | 89970 |
| rs191696037 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219370 | TACTGGGGTGAGATG[A/T]TAGCTCATTGTAGTT | 89970 |
| rs191704761 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239372 | TCTTTATGGAGATGT[A/G]AATGACAGCGTTTCT | 89970 |
| rs191733635 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57190281 | GGCTGAGGTGGTAGA[A/C]TCTCTTGAGCCTGGG | 89970 |
| rs191919261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193881 | GACCAGCCTAGCCCA[C/T]ATGGTGAAACCCCAT | 89970 |
| rs192115899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188640 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGATT | 89970 |
| rs192163381 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235041 | TGTCACAGGTGCAGA[A/G]CATTTTCAAAACATT | 89970 |
| rs192207391 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213787 | AGGCTTTAATAAGAT[A/C]ATGTGCATGAAAGAG | 89970 |
| rs192211472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222781 | TAGAACTAGAAGTAA[C/T]AGGGGATTCTTCCAG | 89970 |
| rs192218064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235718 | AGAGCAGTTGGGCAA[C/T]GTGGCGTCCTGGCCA | 89970 |
| rs192250224 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185599 | GTGTTGGGCCCGCCT[C/G]AAAGGGTCCTCGCCG | 89970 |
| rs192398499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234540 | GGCACACAGTAAGCC[C/T]GTAAGTGAACTGAAT | 89970 |
| rs192406627 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197794 | AATGACACCATTAGG[G/T]CTCACTGCAGCCTCG | 89970 |
| rs192413648 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224925 | ACATTAGAAGGTGAA[A/G]ATAGAAAAGAATTGC | 89970 |
| rs192510352 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215531 | TAGACCTTTCCTTAA[A/C]GGGGAACTCATGTGA | 89970 |
| rs192644981 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206429 | ATTAATCAAAAAAAA[A/T]TTTTTAAATCCCTTG | 89970 |
| rs192656852 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204250 | TGTGGTTTTAAAAAA[A/C]TCAATGATAACTCCT | 89970 |
| rs192669033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229396 | CCTTTGAGAGGATCA[C/T]TTGGGGCCAGGAGTT | 89970 |
| rs192787433 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185402 | GTACATGGCACACAA[C/T]AAATGTGCTTCCCAT | 89970 |
| rs192818741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192073 | GGAGAGACTTTATGT[C/T]ACAGATTTTAGAATA | 89970 |
| rs192825316 | snp | G/T | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240089 | AATTCATAGAACTTC[G/T]TTTATAATGGTGTAC | 89970 |
| rs192901465 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230932 | AAATTGATTAATTTC[A/T]AGTGATTGGGAACCC | 89970 |
| rs192945284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224549 | AATACCAAGCTAACC[A/G]CTCTATTCTCTCATT | 89970 |
| rs192996542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212830 | ATGTTGGCCAGGCTG[G/T]TGTCGAACTCTTGAC | 89970 |
| rs193027281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220102 | TGATTCCTCCAGTTT[C/T]GTTTTCTTGCTGAGG | 89970 |
| rs193071654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212202 | GGTAGTCCCAGCTAC[A/G]AGGGAGGCTGAAGTG | 89970 |
| rs193174871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196627 | GATCAAGCTACAATC[C/T]CTCCCAAGATTCTCT | 89970 |
| rs193238013 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57184536 | GAATGAAGACAAAGT[A/C]TGTTCAAAAGGTGAC | 89970 |
| rs199501379 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192591 | AAAGGATTTGTCTTT[A/T]CTCCTTTGTACCATT | 89970 |
| rs199502191 | snp | A/T | 0.00199792 | 0.0315431 | missense | RSPRY1 | GRCh38.p7 | 16:57220755 | GAAGGTAGACAGCTG[A/T]CCTATGAGAAAGTGA | 89970 |
| rs199503092 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216836 | CCCCTCCTTAGCAAT[-/G]ACTAATTTGCTGAGC | 89970 |
| rs199506613 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192664 | CACTGCTACTAGGTT[-/A]AAAAAAGCTCTCAAC | 89970 |
| rs199611065 | snp | G/T | 0.000317697 | 0.0125995 | missense | RSPRY1 | GRCh38.p7 | 16:57230719 | CCTCTAGGAGATACA[G/T]TAGGATTTCTGTTAG | 89970 |
| rs199640592 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204879 | CCACTGCTGACACAA[A/G]GAGCCAACCACGGGA | 89970 |
| rs199726094 | snp | A/C | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240352 | ATCCACACACACACA[A/C]ACACACAAAAAATAT | 89970 |
| rs199728316 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200947 | GACGGGGCGGCTGGC[-/C]GGGGGGGGGGGGGGC | 89970 |
| rs199738926 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219546 | ATATGACCTCCTTAT[A/G]TATTCTGGTTATTAA | 89970 |
| rs199786106 | in-del | -/ACATTA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197926 | AAATGGGGTCTTGCT[-/ACATTA]CCCAAGCTGGTCTCA | 89970 |
| rs199798795 | in-del | -/T | 0.0162398 | 0.0886349 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240308 | TGTTGGGGTGCTGGA[-/T]TTTTTTCCGTGTCTT | 89970 |
| rs199819083 | in-del | -/CCT | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187524 | GGAGTGACTTAACCT[-/CCT]TAAGTCTCTACTGTA | 89970 |
| rs199854828 | snp | A/T | 0.488314 | 0.0755423 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216088 | TTTTTTTTTTTTTTT[A/T]TCTTTTGTTGTTTTT | 89970 |
| rs199860308 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208396 | TATATATATATATAT[A/T]TATATTTTTTTTTTT | 89970 |
| rs199885931 | in-del | -/AC/CT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231769 | ACATCTTTTAGCAGA[-/AC/CT]CTCGGCTTTATTGAA | 89970 |
| rs199958616 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196036 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 89970 |
| rs200087460 | in-del | -/TC | 0.0189856 | 0.0955633 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206757 | TTTTGTAGAGCCAGG[-/TC]TCTTGCCATGTTGCC | 89970 |
| rs200103588 | in-del | -/CACACAC | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57240352 | ATCCACACACACACA[-/CACACAC]AAAAAATATATATAT | 89970 |
| rs200183473 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210073 | CTCCCTTCCTTCCTT[-/C]CTTTCCTTCCCTTTC | 89970 |
| rs200192613 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204177 | TAAAAGGAGCCCTTG[-/A]AAAAAAAATGCACAC | 89970 |
| rs200198665 | in-del | -/ACT | | | utr-variant-3-prime, cds-indel | RSPRY1 | GRCh38.p7 | 16:57239049 | AAAAAGAAAAAAAAA[-/ACT]CTCTAATCAGTTGTA | 89970 |
| rs200229580 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210434 | AAGGCTGGGCGCGGT[A/G]GTTCACGCCTGTAAT | 89970 |
| rs200308767 | snp | A/G | 0.00376765 | 0.0432392 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220880 | AGTTGGACCCTTTGG[A/G]GGATGAGAGGGTAAT | 89970 |
| rs200350314 | snp | A/G | | | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57239040 | GTTGAAAAGAAAAAG[A/G]AAAAAAAAACTCTCT | 89970 |
| rs200353596 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218727 | CACATTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 89970 |
| rs200529111 | in-del | -/TTTA/TTTGT | 0.0134861 | 0.0810011 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188527 | TTTTTTGTTTGTTTG[-/TTTA/TTTGT]TTTTTTGAGACGGAG | 89970 |
| rs200599144 | snp | A/G | 1.64958e-05 | 0.00287187 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213978 | AACTATTTATTCTTA[A/G]TCATCTAGAAGTGGG | 89970 |
| rs200607450 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199441 | AGGTTGCAGTGAGCC[A/G]AGATCGTACCATTGC | 89970 |
| rs200607629 | snp | A/G | 0.000428237 | 0.0146265 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204798 | ATTCCTGTATCTGCC[A/G]AGATGACAGTGGAAC | 89970 |
| rs200626196 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218755 | TTTTTTTTTTTTTTG[-/AG]ACGGAGTCTCGCTCT | 89970 |
| rs200637247 | in-del | -/TATATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202879 | TTTATTACATATGAT[-/TATATA]TATATATATATATAT | 89970 |
| rs200643065 | in-del | -/TA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208377 | GGAGAGGAGATTATT[-/TA]TATATATATATATAT | 89970 |
| rs200647613 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196032 | TCTCAAAAAAAAAAA[A/T]AAATATATATATATA | 89970 |
| rs200661536 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226082 | AACTCCATCTCAAAG[-/A]AAAAAAAAAGAAGAA | 89970 |
| rs200798983 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199895 | TTGTTTTTTTTGTTT[G/T]TTTTTTTTTTTCTTT | 89970 |
| rs200822658 | in-del | -/AAA | 0.0402882 | 0.136092 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203009 | GCCATGAATCTGTCT[-/AAA]ATAATGGAAATAGGC | 89970 |
| rs200835278 | in-del | -/AGGA | 0.0174175 | 0.0916809 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57236518 | AGAGTCAATCCCCAG[-/AGGA]GACTGAAAATCTAAG | 89970 |
| rs200887019 | snp | A/C/T | 3.29654e-05 | 0.00405978 | synonymous-codon, missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204902 | CCACGGGACCCTGTT[A/C/T]GGCCACCAAGGAGGG | 89970 |
| rs200887059 | in-del | -/TC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192712 | TCCAGAGACTCTTTT[-/TC]TTTTTTTTTTTTTTT | 89970 |
| rs201003537 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210026 | TTTCTTCTTTCTTTC[C/T]TTCCCTCCCTCCCTC | 89970 |
| rs201029140 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195664 | GCTTTTTTTTTTTTT[-/T]GTCTCAAAGTTGACT | 89970 |
| rs201071702 | snp | A/C | 0.477588 | 0.103459 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216090 | TTTTTTTTTTTTTAT[A/C]TTTTGTTGTTTTTCA | 89970 |
| rs201113562 | in-del | -/TCTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208983 | TCTATAGACCAAAAG[-/TCTT]TCTTTTAATGTGAAT | 89970 |
| rs201221660 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210049 | CCTCCCTCCCTCCCT[C/T]CCTCCCTTCCTCCCT | 89970 |
| rs201221888 | in-del | -/TATT | 0.00486831 | 0.0490964 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213966 | GTGAGACATCAAAAC[-/TATT]TATTCTTAGTCATCT | 89970 |
| rs201267411 | in-del | -/GTTT/GTTTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188530 | TTTGTTTGTTTGTTT[-/GTTT/GTTTT]TTTGAGACGGAGTTT | 89970 |
| rs201401528 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238027 | ACAAAAATCAGTAGC[C/T]CTTCTAGCTATATGT | 89970 |
| rs201419602 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218735 | CTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 89970 |
| rs201524384 | in-del | -/C | 0.0402882 | 0.136092 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57207890 | AGCACATATGGTATA[-/C]CATTCATCCTTACAG | 89970 |
| rs201540472 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57233326 | CTACAAGTCATCCAC[C/T]CACAGCCACTGCTTC | 89970 |
| rs201544499 | in-del | -/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199839 | TATCAGTGAAATTTC[-/TT]TTTTTTTTTTTTCCC | 89970 |
| rs201569191 | snp | A/G | 0.000115387 | 0.00759474 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204691 | GGCCGTGTTCTTAGC[A/G]AGCAGAAGCCTTGGC | 89970 |
| rs201575473 | in-del | -/ATATA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57208396 | TATATATATATATAT[-/ATATA]TTTTTTTTTTTTTTT | 89970 |
| rs201623716 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231771 | CATCTTTTAGCAGAC[G/T]CGGCTTTATTGAAAC | 89970 |
| rs201634523 | snp | A/G | 6.6024e-05 | 0.00574523 | missense | RSPRY1 | GRCh38.p7 | 16:57235162 | AGCAAGTCAGTATCC[A/G]AGAAAACTGCTGTTC | 89970 |
| rs201685513 | in-del | -/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200561 | GCCTCCCTCCCGGAT[-/G]GGGCGGCTGGCCGGG | 89970 |
| rs201701694 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212731 | GTGATTCTCCTGCCT[A/C]AGCCTCCTGAGTAGC | 89970 |
| rs201838465 | in-del | -/T | 0.0279526 | 0.114869 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222217 | AGTGATCCAACAAAA[-/T]TCAAGCTAAACTTGC | 89970 |
| rs201954899 | snp | G/T | 3.31868e-05 | 0.00407336 | missense | RSPRY1 | GRCh38.p7 | 16:57230778 | TTTAAATGGCAACCA[G/T]CTGCCTCCTGAAAAG | 89970 |
| rs202031312 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237679 | GCTAGTATCTCTTTA[-/T]TTTTTTTATTTTTAT | 89970 |
| rs202092058 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192718 | GACTCTTTTTTTTTT[-/C]TTTTTTTTTTAAGGT | 89970 |
| rs202132521 | snp | C/T | 0.224116 | 0.248656 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201358 | TCCTCACATCCCAGA[C/T]GGGGCGGCAGGGCAG | 89970 |
| rs202149086 | snp | A/G | 0.00199809 | 0.0315445 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57212977 | TTTGTTTTAGGATGC[A/G]CTCCAGAAATTGACT | 89970 |
| rs202167866 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57191639 | TAACTTCATCTTTAT[-/C]AATTTAATTTATAGG | 89970 |
| rs202168996 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218724 | TGCCACATTTTCTTT[A/T]TTTTTTTTTTTTTTT | 89970 |
| rs202227420 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192713 | CCAGAGACTCTTTTT[-/C]TTTTTTTTTTTTTTT | 89970 |
| rs367609887 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198775 | TGGATTGAATCTACT[A/G]TTTGCATCTTGTTTC | 89970 |
| rs367615747 | snp | C/T | 0.000286357 | 0.0119623 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57227350 | TCTCCAGGAAGGCTA[C/T]GGCATTGGGGATGAT | 89970 |
| rs367616751 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200687 | CACCTCCCTCCCGGA[A/C]GGGGCGGCTGGCCGG | 89970 |
| rs367739488 | snp | A/G | 0.00019861 | 0.0099632 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231331 | CAAGGTAAGGAATCT[A/G]CCCAGGCTATCTCCA | 89970 |
| rs367915715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189520 | AAAAAAAAAAAAAGT[A/G]TGTTTTGTCAAGAGT | 89970 |
| rs367917259 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215241 | ATTGTCTGATGAGAG[A/G]AGACAGTGTTCAGAG | 89970 |
| rs367962277 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238833 | GCAGTTGGAGTTTGA[C/T]CTTTTGAAGCATTAA | 89970 |
| rs367993804 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231636 | AACACTTTCAAATTT[G/T]TTTTGTGAGATAAAT | 89970 |
| rs367999357 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202703 | GTGGTTTGGGGGAAC[C/G]AAGAACATCTGTGGT | 89970 |
| rs368063761 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189588 | TTTTCTTTTTCTTTT[C/T]TTTTCTTTTTTTTTT | 89970 |
| rs368089371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237807 | ACCTCCGCCTCCCGA[A/G]CTCAAGTGATTTCTC | 89970 |
| rs368106148 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57196004 | TCCAGCCTGGCGACA[A/G]AGTGAGACTTCATCT | 89970 |
| rs368166957 | snp | C/T | 3.30387e-05 | 0.00406427 | missense | RSPRY1 | GRCh38.p7 | 16:57212978 | TTGTTTTAGGATGCA[C/T]TCCAGAAATTGACTG | 89970 |
| rs368188405 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186480 | CCCGACCGCGCTGCT[C/T]TGAGCCCTGGGCACG | 89970 |
| rs368236422 | snp | A/G | 0.00134536 | 0.0259012 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230668 | GCAAAGAATCCTGGT[A/G]GTACACATCATTATC | 89970 |
| rs368278793 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57237041 | GGCGTGGTGGTGGGC[A/G]CCTGTAATCCCAGCT | 89970 |
| rs368309991 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | RSPRY1 | GRCh38.p7 | 16:57231220 | AACAATGTGAGTTCA[A/G]TTTTGGAGCAAAACC | 89970 |
| rs368358320 | snp | A/G | 0.000250708 | 0.0111934 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221231 | TCTTTGGTGGTCTTC[A/G]GGCCCTCATAGTTGA | 89970 |
| rs368367064 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229473 | AAATTTTAAAAATTT[C/G]CCAGGGGTGGTGGCA | 89970 |
| rs368368825 | in-del | -/T | 0.000150084 | 0.00866137 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221243 | TTCAGGCCCTCATAG[-/T]TGATTGACACATTTT | 89970 |
| rs368389140 | snp | A/T | 1.67528e-05 | 0.00289415 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212936 | AACAACCTGTGTAGT[A/T]TATGGGTCAAACCCA | 89970 |
| rs368451405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219597 | TTGCAAATAGTTTCT[C/T]CCATTCTGTGGGATG | 89970 |
| rs368556984 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57216424 | TTTAGTGATGTGATT[A/G]CTAGTTTCTAGAAAA | 89970 |
| rs368643288 | snp | C/T | 5.09394e-05 | 0.00504649 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235242 | AGGTAAGAGGATTTA[C/T]ATTAGGCAAAGTTTC | 89970 |
| rs368665622 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193598 | TCTGGATTCAAGTGA[G/T]CTTCCCACCTCAGCC | 89970 |
| rs368750011 | in-del | -/GGG | | | utr-variant-3-prime, cds-indel | RSPRY1 | GRCh38.p7 | 16:57239611 | GTTTTTTTGTTTTTT[-/GGG]TTTTTTTTTTTTACT | 89970 |
| rs368822955 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230244 | TTCAAACTCCTGACC[C/T]CAGGTGATCCGCCCG | 89970 |
| rs368838383 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | RSPRY1, FAM192A | GRCh38.p7 | 16:57186040 | CCTCACCGCCACAAT[A/G]GAGTCCCGCCCCACT | 89970 |
| rs369029132 | snp | C/T | 3.29641e-05 | 0.00405968 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204694 | CGTGTTCTTAGCGAG[C/T]AGAAGCCTTGGCCAG | 89970 |
| rs369031935 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200033 | AGGTCTCTGGTTTTC[C/T]TAGGCAGAGGACCCT | 89970 |
| rs369039803 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187891 | GTGCTGGCAGGAGTT[A/G]CCACTGTAATATCTT | 89970 |
| rs369095150 | snp | C/T | 1.66463e-05 | 0.00288494 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231355 | ATCTCCAGACTTTCA[C/T]ATGAATCTTATGAGA | 89970 |
| rs369122446 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225985 | CAGGAGGCTGAGGCA[G/T]GAGAATCGCTTAAAC | 89970 |
| rs369138781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199013 | CCTTCTACCATCCCC[A/T]AAGTGTTAGTTGGGT | 89970 |
| rs369220066 | snp | A/G | 0.00117379 | 0.0241974 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238994 | ATGTGAAGAGGCATC[A/G]TGGACTTTTTTCTAC | 89970 |
| rs369277297 | snp | A/G | 9.88875e-05 | 0.00703093 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217068 | TTTATTAAAATGTCC[A/G]TTTCCATTTCCAGAC | 89970 |
| rs369322843 | in-del | -/AT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230901 | TTTGTCCATTTATAT[-/AT]GCAATTGTGATGAGA | 89970 |
| rs369418901 | snp | A/G | 1.67066e-05 | 0.00289016 | utr-variant-3-prime | RSPRY1 | GRCh38.p7 | 16:57238986 | CATGACACATGTGAA[A/G]AGGCATCGTGGACTT | 89970 |
| rs369463377 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211387 | CCAGCCTGGCCAACA[C/T]GGTGAAACCTCATCT | 89970 |
| rs369476435 | snp | C/T | 1.65299e-05 | 0.00287483 | missense | RSPRY1 | GRCh38.p7 | 16:57220836 | CTGAAGATCTCACCT[C/T]ATGGCTTAGAGGTAG | 89970 |
| rs369496033 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217935 | ATTTGGATTTTGTTC[A/T]TACAAAATTATATTC | 89970 |
| rs369512882 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186287 | AAGGGGCGTTTCCTA[A/G]GGGACTGAGGGAGGG | 89970 |
| rs369519367 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213164 | AGGGAAATTTGTACT[C/G]TATGTCTTTGATCAA | 89970 |
| rs369535247 | snp | C/G/T | 3.41683e-05 | 0.00413318 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230705 | GTGTTTCTCTTTATC[C/G/T]TCTAGGAGATACAGT | 89970 |
| rs369554037 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | RSPRY1 | GRCh38.p7 | 16:57216993 | CCTGATTATCTGAAA[C/T]GTCAAGTTGGTTTCT | 89970 |
| rs369588365 | snp | C/T | 9.88663e-05 | 0.00703018 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213879 | CAAGTGTTTGTTGTA[C/T]TTGTCTAGGTCCTGC | 89970 |
| rs369596867 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230660 | GATGCTTAGCAAAGA[A/G]TCCTGGTAGTACACA | 89970 |
| rs369691888 | snp | A/G | | | intron-variant, downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57205397 | GTAAGTTGTTTTACC[A/G]AGAACATGGCTACAG | 89970 |
| rs369700058 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234062 | GACCTCCCAGGCCCC[A/G]TACAATTTGTCCTCT | 89970 |
| rs369718026 | in-del | -/GAGTTTTA | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57229663 | AACCTTAGAGTTTTA[-/GAGTTTTA]CTTTATCTGATAAGT | 89970 |
| rs369756896 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232517 | AAAGTCTGAGGGGAC[A/T]CCTCTCCCTTATCTA | 89970 |
| rs369768929 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231734 | GTCAGTGTCAAAATC[C/T]TAAATATTAGGAAAT | 89970 |
| rs369821364 | in-del | -/CC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200379 | TTCTATTCCACAAAA[-/CC]CCGCCATTGTCATCA | 89970 |
| rs369868687 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218728 | ACATTTTCTTTTTTT[A/T]TTTTTTTTTTTTTTT | 89970 |
| rs369878457 | snp | C/T | 0.16846 | 0.236329 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200850 | AGGCGCCCCTCACCT[C/T]CCGGACGGGGCGGCT | 89970 |
| rs369909889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57232410 | GTTGCATATGTTCCC[G/T]CTCAGGGTTCTGAGG | 89970 |
| rs369912404 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240535 | TATACTCTCAGACTT[C/T]AAGGGCTACTTTTGG | 89970 |
| rs369918503 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204690 | GGGCCGTGTTCTTAG[C/T]GAGCAGAAGCCTTGG | 89970 |
| rs370021384 | snp | C/T | 1.78245e-05 | 0.00298529 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230851 | AAATTCGAGTAGATG[C/T]ACGGAATGCCCTTTT | 89970 |
| rs370126233 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57226511 | GACAGGCAATTCCTG[A/G]AACCAAGGGTTCCTC | 89970 |
| rs370148194 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219500 | TTTGCCCACTTTTTA[A/G]TCAGATTATTGAATG | 89970 |
| rs370209280 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189577 | TTTTTTCTGTTTTTT[C/T]TTTTTCTTTTCTTTT | 89970 |
| rs370281497 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188581 | GAGTGCAGTGGCGCT[A/G]TCTCGGCTCACTGCA | 89970 |
| rs370293183 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227723 | TATGAATTCTATTTT[C/T]CTCTTTGGATCTGTT | 89970 |
| rs370294729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57228659 | TACTTAATACCTTGA[A/G]CAGCTTTCCAGGTTA | 89970 |
| rs370481555 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206331 | GTACTGCTAGAGTCC[A/C]GGAGTTTCCAGCTGC | 89970 |
| rs370488132 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57203804 | TTCTGAACTTTGTAA[C/T]AGACATGTGCAACAA | 89970 |
| rs370494653 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201381 | CAGGGCAGAGGCACT[A/C]CCCACATCTCAGACG | 89970 |
| rs370495500 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57198188 | CAGGAGATCGAGACT[A/T]TCCTGACTAACACAG | 89970 |
| rs370604227 | snp | A/G | 5.01073e-05 | 0.00500511 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221233 | TTTGGTGGTCTTCAG[A/G]CCCTCATAGTTGATT | 89970 |
| rs370676894 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188990 | TCTGTACTCAGTGAC[-/T]TTTTTTTTTTTTTTT | 89970 |
| rs370709393 | in-del | -/TC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199837 | CTTATCAGTGAAATT[-/TC]TTTTTTTTTTTTTTC | 89970 |
| rs370722558 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201214 | GACGGTGTGGCTGCC[A/G]GGCGGAGGGGCTCCT | 89970 |
| rs370723428 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57234517 | CTCTAGGGCTTGGAA[C/T]AGTGCCTGGCACACA | 89970 |
| rs370760589 | in-del | -/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238721 | CAGAAATGTAAGATT[-/T]ACTTTTTATTTACAT | 89970 |
| rs370815861 | in-del | -/TC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231771 | CATCTTTTAGCAGAC[-/TC]GGCTTTATTGAAACA | 89970 |
| rs370883679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220564 | ATTTTTTTAGGTTTT[C/T]CTAAATATAAGATCA | 89970 |
| rs370886194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230254 | TGACCTCAGGTGATC[C/T]GCCCGCCTTGGCCTC | 89970 |
| rs370892910 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186334 | CGGGGGTGGGCTCTG[A/C]GCGTAATGGCAGCGC | 89970 |
| rs370948114 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189593 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 89970 |
| rs370996229 | snp | A/G | 0.000469673 | 0.0153172 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231138 | ATTTTTATTAATTCT[A/G]TTGGCCTCTGTACTC | 89970 |
| rs371095165 | snp | A/G | 1.66062e-05 | 0.00288146 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209226 | GAAACTATCATTTGT[A/G]CTTAAGCACAAGATA | 89970 |
| rs371468313 | snp | A/G | 1.68221e-05 | 0.00290014 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57235235 | TGGACACAGGTAAGA[A/G]GATTTATATTAGGCA | 89970 |
| rs371561971 | snp | A/G | 0.000314125 | 0.0125285 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209198 | CTAAAGTAAGTTAAT[A/G]CTTATCTTTTATGAA | 89970 |
| rs371659385 | snp | A/G | 0.000181454 | 0.00952334 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221430 | TGTGAGTACCCTAGA[A/G]AACTGTGAAAATGGG | 89970 |
| rs371661904 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204719 | GGCCAGGGTCTGTTG[C/T]TGACTCTCGAAGAGC | 89970 |
| rs371669970 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200701 | ACGGGGCGGCTGGCC[A/G]GGCAGAGGGGCTCCT | 89970 |
| rs371679964 | snp | A/G | 0.000153988 | 0.00877328 | splice-donor-variant | RSPRY1 | GRCh38.p7 | 16:57213099 | CCGAGAAACTAGCAG[A/G]TAACTTTGGGACACT | 89970 |
| rs371684230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202097 | AGGCCAAGATGAGAG[C/G]ATTATTTGAGGCTAG | 89970 |
| rs371699208 | snp | A/C | 4.99189e-05 | 0.00499569 | utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204648 | TACTTGGAAAACTGA[A/C]AACTACCTAAATGAT | 89970 |
| rs371813417 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212946 | GTAGTATATGGGTCA[A/G]ACCCACTTGTACTTT | 89970 |
| rs371834894 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57215262 | GTGTTCAGAGATAGG[A/G]CACAGACTGAGTAGC | 89970 |
| rs371903574 | in-del | -/CCTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210061 | CTTCCTCCCTTCCTC[-/CCTT]CCTTCCTTCCTTCTT | 89970 |
| rs372002819 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185595 | GGCAGTGTTGGGCCC[C/G]CCTGAAAGGGTCCTC | 89970 |
| rs372042318 | in-del | -/TGTTTT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197732 | TTTTGTTTTTGTTTT[-/TGTTTT]CCCAAAGACAGGGTC | 89970 |
| rs372069179 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199212 | GATTTAAAGAAAAAG[C/T]GGCTGGGCGCGGCGG | 89970 |
| rs372098104 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224950 | AATTGCTTGCCTTTT[A/C]CTTATGCCACAATGC | 89970 |
| rs372183285 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57185764 | GCAGCTCATCTCTTC[A/C]GTAAGGAAGCTGGAA | 89970 |
| rs372222224 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189839 | CAAGCCATCCACCCA[-/C]CTTGGCCTCCCAAGG | 89970 |
| rs372267250 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57197617 | TAAGGAAAATTGCTC[C/T]TTTGGAAGAAACTGA | 89970 |
| rs372347740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199059 | ATAGCATAGTGGTCA[A/G]GAAATTATGATAATA | 89970 |
| rs372397079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218324 | TCCAATTATACTCTT[C/T]TGGTGTTTTAAAATT | 89970 |
| rs372465412 | snp | G/T | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187912 | GTAATATCTTTTCCT[G/T]CAGGAATTATTTTCC | 89970 |
| rs372540869 | snp | A/G | | | downstream-variant-500B | RSPRY1 | GRCh38.p7 | 16:57240912 | ATTTGTGTTTATTGT[A/G]ACAGATTTTTAGTGG | 89970 |
| rs372545171 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218938 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 89970 |
| rs372571451 | snp | A/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200112 | GGTGATGACTCTTAA[A/C]GAGCATGCTGCCTTC | 89970 |
| rs372622407 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192355 | AAACCACAAGTACTA[A/C/T]GGAATATTACATTTG | 89970 |
| rs372645078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194481 | ACTTAGGGAAAAATC[C/T]GAAAACATTTTCTAA | 89970 |
| rs372653691 | snp | C/G | 1.67304e-05 | 0.00289222 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57238834 | CAGTTGGAGTTTGAC[C/G]TTTTGAAGCATTAAC | 89970 |
| rs372798463 | snp | A/G | 1.64825e-05 | 0.00287071 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213867 | TTTTAATTATATCAA[A/G]TGTTTGTTGTATTTG | 89970 |
| rs372809294 | snp | G/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57186853 | TGACCTACTCAGGGG[G/T]GCCCGGGATAGAAAG | 89970 |
| rs372813239 | snp | A/G | 1.65414e-05 | 0.00287583 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57227401 | TGGCTGCCGGCAGCT[A/G]ATTTGGTACAATGCC | 89970 |
| rs372846087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57222234 | CAAGCTAAACTTGCC[A/G]GCCATAAGTATGGTG | 89970 |
| rs372893786 | snp | A/G | 3.3024e-05 | 0.00406336 | missense | RSPRY1 | GRCh38.p7 | 16:57208095 | ATGATAACATTACAC[A/G]AAATGGCAGAAACAG | 89970 |
| rs373097597 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57206934 | ACTTTTCTCAACATC[A/G]AAATCTGTGTTACTG | 89970 |
| rs373251955 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187016 | AGCTAGAACTAGCGG[A/T]ATGTCCTACTACGGA | 89970 |
| rs373324351 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57219685 | TCCCATTTGTCCATT[A/T]TTGCTTTGGTGCCTG | 89970 |
| rs373352754 | in-del | -/TCG | | | upstream-variant-2KB, utr-variant-5-prime | RSPRY1, FAM192A | GRCh38.p7 | 16:57186174 | CTCAGGATGAGGACT[-/TCG]GGCCAGTCTGCGCCT | 89970 |
| rs373426060 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199286 | GATCACGAAGTCAAG[A/G]GTTTGAGACCAGCCT | 89970 |
| rs373562882 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57201217 | GGTGTGGCTGCCGGG[C/T]GGAGGGGCTCCTCAC | 89970 |
| rs373569327 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57227771 | TGGCAATATCAGGGA[C/T]ACTGGAATTGTAATG | 89970 |
| rs373754710 | snp | C/T | 4.94262e-05 | 0.00497098 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57213904 | TCCTGCAAGTATAGG[C/T]TTACTTAGCCCAGGA | 89970 |
| rs373877320 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231329 | GCCAAGGTAAGGAAT[C/G]TGCCCAGGCTATCTC | 89970 |
| rs373914013 | in-del | -/T/TT | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57192708 | TTTTTCCAGAGACTC[-/T/TT]TTTTTTTTTTTTTTT | 89970 |
| rs373922698 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189583 | CTGTTTTTTCTTTTT[C/T]TTTTCTTTTCTTTTT | 89970 |
| rs373933055 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212014 | GCCTGTTTCAATTTG[C/T]CTTCAACTCTGTTGG | 89970 |
| rs374004464 | snp | C/T | 1.65784e-05 | 0.00287905 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57212968 | TTGTACTTTTTTGTT[C/T]TAGGATGCACTCCAG | 89970 |
| rs374064986 | in-del | -/A | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57211003 | GCCTGGTTAAAAAAA[-/A]GAAGTATTTGTATCT | 89970 |
| rs374083102 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57214808 | CTGAGGTGGGCTGGT[C/T]ACCTGAGGTCAGGAG | 89970 |
| rs374162161 | snp | C/T | 0.283158 | 0.247791 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57200886 | GGCAGAGGGGCTCCT[C/T]ACTTCCCAGTAGGGG | 89970 |
| rs374205065 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189435 | ATTTTGTATAATAGT[A/G]TGTTAATCTGTAGTG | 89970 |
| rs374269118 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57213831 | ATTTGATTGTTACCA[A/G]TGATTTAAAATAATC | 89970 |
| rs374269792 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189820 | GGTCTCAAACTCCTG[G/T]GCACAAGCCATCCAC | 89970 |
| rs374336718 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57230338 | TTTTTAAAGAAAGGC[A/G]TATTTTGGGGTAGTT | 89970 |
| rs374355145 | snp | A/T | | | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204995 | CTGGCAGTAATACGG[A/T]CTCTTGTAGATAAGT | 89970 |
| rs374438951 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193506 | CTTTTTTTTTTTTTT[C/T]TTTGGAGACAGAGTC | 89970 |
| rs374482375 | snp | A/C | 1.6628e-05 | 0.00288335 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209231 | TATCATTTGTGCTTA[A/C]GCACAAGATAAATGA | 89970 |
| rs374509359 | in-del | -/TTTTC | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57218716 | TGTATATGTGCCACA[-/TTTTC]TTTTTTTTTTTTTTT | 89970 |
| rs374528362 | snp | A/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57204038 | AACAAACGTCTGTAA[A/T]TATTTTATTTAAAAC | 89970 |
| rs374605387 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57188531 | TTTGTTTGTTTGTTT[G/T]TTGAGACGGAGTTTC | 89970 |
| rs374914169 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217055 | GTGGGAGTTGTCCTT[C/T]ATTAAAATGTCCGTT | 89970 |
| rs374928871 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | RSPRY1 | GRCh38.p7 | 16:57204797 | AATTCCTGTATCTGC[C/G]GAGATGACAGTGGAA | 89970 |
| rs375003667 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57194332 | AAAATGTTAGTAGTA[G/T]AATCTAGGTGGTGGG | 89970 |
| rs375007311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57231631 | GACGGAACACTTTCA[A/G]ATTTTTTTTGTGAGA | 89970 |
| rs375010908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57193779 | GCTTAAGATTTGCAC[A/G]TTTCAGCCGGGTGCG | 89970 |
| rs375022099 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57199746 | GCACAATCATCTGAC[C/T]TACTGGCCCAGAGCC | 89970 |
| rs375074697 | snp | C/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217368 | CAGGTCCTGATGATT[C/G]CTACCTCTGGACCTA | 89970 |
| rs375168558 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195959 | CCCAGGAGATAGAGG[C/T]TGCAGTGAGCCGAGA | 89970 |
| rs375205704 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57224994 | GTTTTTAAGTTTTTT[A/G]CTTACTGACTTGTTC | 89970 |
| rs375335685 | snp | C/T | 1.65002e-05 | 0.00287225 | synonymous-codon | RSPRY1 | GRCh38.p7 | 16:57231188 | TGACTACGCCTTCC[C/T] | 89970 |
| rs375513384 | snp | A/G | 0.000131781 | 0.00811621 | missense | RSPRY1 | GRCh38.p7 | 16:57216946 | CCAGTATTAGTGACC[A/G]GCTTGTCACATTGGA | 89970 |
| rs375578147 | snp | A/G | | | upstream-variant-2KB, intron-variant | RSPRY1, FAM192A | GRCh38.p7 | 16:57185489 | GAGTAACCTGGACCT[A/G]TTCCAAGACCTCTGG | 89970 |
| rs375645406 | snp | G/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57189570 | TATTTCTTTTTTTCT[G/T]TTTTTTCTTTTTCTT | 89970 |
| rs375646180 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221141 | TTGTCACTGAGGATG[A/G]ACAGAGGAGGAAGCA | 89970 |
| rs375654242 | snp | C/T | 1.65021e-05 | 0.00287241 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57209070 | TCTTCTTGATTTGCT[C/T]TTAGATGAAGGATGG | 89970 |
| rs375727886 | snp | A/G | | | intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187689 | AGAGGTAAGGGGTGG[A/G]ATTAATACAGTCGTT | 89970 |
| rs375747843 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57195168 | AGAAATAGATTTGCA[A/G]AGGAAATATTCGATC | 89970 |
| rs375748508 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | RSPRY1 | GRCh38.p7 | 16:57217052 | TAAGTGGGAGTTGTC[C/G]TTTATTAAAATGTCC | 89970 |
| rs375748754 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57221813 | TTTCAAAAAATAGAG[C/T]GTTGGCTTGACTTCT | 89970 |
| rs375914200 | in-del | -/C | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57210844 | CAACATGGTGAAACC[-/C]TGTTTCTACAAAAAA | 89970 |
| rs375986489 | in-del | -/AG | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57225084 | TTTTGTTTTGAGACA[-/AG]GTCTCGCTCTGTCAC | 89970 |
| rs376254396 | snp | C/T | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57202342 | ATTTCTGTGAGAGGA[C/T]CCAGAGCATAGCTTC | 89970 |
| rs376324013 | snp | A/C | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RSPRY1, FAM192A | GRCh38.p7 | 16:57187045 | GAAGCCGGAGCTGAA[A/C]ATTGGGTAAGGACCT | 89970 |
| rs376326274 | snp | A/G | | | intron-variant | RSPRY1 | GRCh38.p7 | 16:57220504 | TTAATTTTATATCCT[A/G]CAACTTTACTGAATT | 89970 |