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 |