SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14998 | snp | A/T | 0 | 0 | utr-variant-3-prime | USP37 | GRCh38.p7 | 2:218450371 | TCTGCTAAAACACAG[A/T]TAAAAGTGCCGCTCC | 57695 |
rs471846 | snp | C/T | 0.499923 | 0.00618962 | upstream-variant-2KB, intron-variant | CNOT9, USP37 | GRCh38.p7 | 2:218567514 | ATATCCAACTGCCTA[C/T]TTGACATTCCCTCTC | 57695 |
rs483172 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218563576 | TTCTCAAATTAGGCT[C/T]CACTAGGCCTGAACT | 57695 |
rs484085 | snp | A/G | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218531961 | tggtttctttaccag[A/G]attagatttcatctc | 57695 |
rs485975 | snp | C/T | 0.389152 | 0.207694 | intron-variant | USP37 | GRCh38.p7 | 2:218509527 | GCTGAGGAGGGAGGA[C/T]TGCTTGAGGCCAGGA | 57695 |
rs490483 | snp | A/T | 0.38821 | 0.208322 | intron-variant | USP37 | GRCh38.p7 | 2:218564329 | tcaatttaattttta[A/T]aataatcctaagtga | 57695 |
rs492400 | snp | C/T | 0.4776 | 0.103433 | intron-variant | USP37 | GRCh38.p7 | 2:218485029 | CTTAGAATGAAGGAA[C/T]GCACAAACTGCAAAA | 57695 |
rs492625 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | USP37 | GRCh38.p7 | 2:218465480 | ACTAGGAATAATCTA[C/T]AATACCCCATCCTGT | 57695 |
rs495855 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | USP37 | GRCh38.p7 | 2:218493135 | AAGTACATTTGCCAA[A/G]CTGGCCAAACAAACC | 57695 |
rs496674 | snp | A/G | 0.387832 | 0.208572 | upstream-variant-2KB, intron-variant | CNOT9, USP37 | GRCh38.p7 | 2:218567846 | CATGTCCAAGGCCTG[A/G]TGGATGTGCCGTAAC | 57695 |
rs496908 | snp | A/T | 0.433236 | 0.170072 | intron-variant | USP37 | GRCh38.p7 | 2:218493019 | cttaaaaaaaaaaaa[A/T]TTTTTTTCCCTCATA | 57695 |
rs497983 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | USP37 | GRCh38.p7 | 2:218550466 | CAAATGGTCATCAGT[C/T]GGAAATTGGCTAACC | 57695 |
rs500317 | snp | C/G | 0.447291 | 0.153545 | upstream-variant-2KB, utr-variant-5-prime | CNOT9, USP37 | GRCh38.p7 | 2:218568230 | GAAAGCACGGAGCCC[C/G]CGAGGAGTGGGAGGA | 57695 |
rs500422 | snp | A/C | 0.499104 | 0.0211472 | upstream-variant-2KB, utr-variant-5-prime | CNOT9, USP37 | GRCh38.p7 | 2:218568272 | TGGAAGTAGGGATAC[A/C]GAACCCAAAGGAGGG | 57695 |
rs502196 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP37 | GRCh38.p7 | 2:218523571 | AAGCTGTTTTTTGGC[A/G]GGGGGgtcttttttc | 57695 |
rs511080 | snp | A/G | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218469890 | cagtggcaccatctc[A/G]actcactgcaacctc | 57695 |
rs514356 | snp | C/T | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218510295 | GGAAAACTCTACAAA[C/T]GTAAATTAGCAAATC | 57695 |
rs514799 | snp | C/T | 0.387642 | 0.208697 | intron-variant | USP37 | GRCh38.p7 | 2:218546480 | GGTGAGCCAAGATCA[C/T]GTCACTACACTTCAG | 57695 |
rs520095 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | USP37 | GRCh38.p7 | 2:218464762 | ATGGCATAAACTGAA[C/T]ATTGAAGAATAGGTT | 57695 |
rs520781 | snp | C/T | 0.031825 | 0.122064 | intron-variant | USP37 | GRCh38.p7 | 2:218473815 | GCTTAATGATGAAGA[C/T]ACATTCTAAGAAATT | 57695 |
rs523305 | snp | A/G | 0.388021 | 0.208447 | intron-variant | USP37 | GRCh38.p7 | 2:218537968 | CATGGGTGTGATAGC[A/G]CTTAGCTCCTGATGG | 57695 |
rs523396 | snp | G/T | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218474066 | CAGGGAATGGAGAAC[G/T]TGAATTATTTATACC | 57695 |
rs524012 | snp | G/T | 0.447032 | 0.153878 | upstream-variant-2KB | CNOT9, USP37 | GRCh38.p7 | 2:218568550 | CCCCCACCATTTCCC[G/T]CCTACGCAACCCAGT | 57695 |
rs524902 | snp | A/C | 0.499866 | 0.0081858 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CNOT9, USP37 | GRCh38.p7 | 2:218568634 | ACTGGCTTTTGGAGG[A/C]GGGTCAGAGTTCACG | 57695 |
rs526134 | snp | C/T | 0.447162 | 0.153712 | intron-variant | USP37 | GRCh38.p7 | 2:218537648 | TTATTTACCTGATAT[C/T]ACCTACATCttatct | 57695 |
rs526897 | snp | A/G | 0.387832 | 0.208572 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CNOT9, USP37 | GRCh38.p7 | 2:218568874 | CTACGGCGGCTCATT[A/G]TTTTCCGCTGCAGGG | 57695 |
rs532425 | snp | A/G | 0.387453 | 0.208822 | intron-variant, upstream-variant-2KB | CNOT9, USP37 | GRCh38.p7 | 2:218569471 | ACTTAGGTTCTCTGC[A/G]TTTAAAACTTTTCCT | 57695 |
rs532475 | snp | C/T | 0.447032 | 0.153878 | intron-variant, upstream-variant-2KB | CNOT9, USP37 | GRCh38.p7 | 2:218569485 | CATTTAAAACTTTTC[C/T]TCGACACATCTCGTT | 57695 |
rs533760 | snp | C/T | 0.387642 | 0.208697 | intron-variant | USP37 | GRCh38.p7 | 2:218516682 | cttgcacattctgca[C/T]gtgtcccagaactta | 57695 |
rs535830 | snp | C/G | 0.499913 | 0.00658888 | intron-variant | USP37 | GRCh38.p7 | 2:218507510 | ACTTCATGGTTTGTT[C/G]TAGGGGGCAGAATTT | 57695 |
rs537520 | snp | C/T | 0.447291 | 0.153545 | intron-variant | USP37 | GRCh38.p7 | 2:218517129 | TGCATTTTTGATATA[C/T]TGAAGTCTAATGTAG | 57695 |
rs539451 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218562249 | ATGATCCAGTAACAG[C/T]TAAACTTCCTATGAA | 57695 |
rs541000 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218526949 | gcccgccaccacgcc[C/T]ggctaattttttgta | 57695 |
rs541860 | snp | C/T | 0.402277 | 0.198272 | intron-variant | USP37 | GRCh38.p7 | 2:218527032 | CGACCTCGTGATCCA[C/T]CCGCCTCGGCCTCCC | 57695 |
rs545179 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | USP37 | GRCh38.p7 | 2:218545416 | GTTCTGCCATCCTTA[A/C]TTAATAAGCAGCCTC | 57695 |
rs545460 | snp | A/G | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218527436 | TACATTTAGTTCCCA[A/G]TCTCGTGCTGGTTTG | 57695 |
rs545779 | snp | A/G | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218471385 | gaattaatatcagaa[A/G]ctgagaaaacaggct | 57695 |
rs547508 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | USP37 | GRCh38.p7 | 2:218481041 | AAAAACCTCTAAAAT[C/G]TCTTCCATCTTCAAA | 57695 |
rs548521 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | USP37 | GRCh38.p7 | 2:218463958 | tgagacaggagaatc[A/G]cttgaacctgggagg | 57695 |
rs549026 | snp | A/G | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218474560 | TTTGTAGTGACAAAT[A/G]ACCTCCAAATAACGG | 57695 |
rs552882 | snp | C/T | 0.447162 | 0.153712 | intron-variant | USP37 | GRCh38.p7 | 2:218537003 | tccattaccccaaTA[C/T]GATCTATTGTGTAAT | 57695 |
rs556468 | snp | A/G | 0.387642 | 0.208697 | intron-variant | USP37 | GRCh38.p7 | 2:218491071 | agagaagagggtatc[A/G]ctatgttgtcagggc | 57695 |
rs558050 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | USP37 | GRCh38.p7 | 2:218556264 | TTTCATGTATTTGTC[C/T]ACATACAGAAATCAC | 57695 |
rs559722 | snp | C/T | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218533436 | GGAACAAAACGTAGA[C/T]GTTTTAAATGTGTTA | 57695 |
rs561570 | snp | A/T | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218514625 | ctctacagtgaagtt[A/T]ctatttttccttttg | 57695 |
rs563153 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | USP37 | GRCh38.p7 | 2:218524193 | TTTTCTGTGTTCATA[A/T]GTGAAAAACTATAAT | 57695 |
rs563268 | snp | G/T | 0.499908 | 0.00678851 | intron-variant | USP37 | GRCh38.p7 | 2:218508189 | TGGTTAATCTTATGG[G/T]TTTTTTTGGAGGATT | 57695 |
rs564509 | snp | C/T | 0.447291 | 0.153545 | intron-variant | USP37 | GRCh38.p7 | 2:218468290 | gctcattgcaacctc[C/T]acctcccgggttcaa | 57695 |
rs566082 | snp | A/G | 0.299916 | 0.244966 | intron-variant | USP37 | GRCh38.p7 | 2:218562902 | GGCACGGTGGCTGAC[A/G]CGAGTAATCCCAGCA | 57695 |
rs570790 | snp | A/G | 0.499923 | 0.00618962 | intron-variant | USP37 | GRCh38.p7 | 2:218471842 | accagcctggccaac[A/G]tggtgaatccccatg | 57695 |
rs573555 | snp | A/C | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218484165 | ctctgtttgaaaaaa[A/C]caaaaaaCACAACat | 57695 |
rs574759 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | USP37 | GRCh38.p7 | 2:218528285 | CTCACTTTTTTTTTT[A/T]Aattatattttaagt | 57695 |
rs576901 | snp | C/T | 0.38821 | 0.208322 | intron-variant | USP37 | GRCh38.p7 | 2:218559641 | GTTCATTCAGGAAAC[C/T]TGAGTATTTGTTAAA | 57695 |
rs578450 | snp | A/G | 0.388021 | 0.208447 | intron-variant | USP37 | GRCh38.p7 | 2:218536514 | TTTTAATCCAAATCA[A/G]GAGAGCTGGGCTTCT | 57695 |
rs579610 | snp | G/T | 0.44755 | 0.153212 | intron-variant | USP37 | GRCh38.p7 | 2:218462859 | TACCTCCCAGGTAAA[G/T]AAATAGAACCTTAGA | 57695 |
rs581013 | snp | G/T | 0.388021 | 0.208447 | upstream-variant-2KB, intron-variant | CNOT9, USP37 | GRCh38.p7 | 2:218567317 | ATTGGTTATTAAACA[G/T]CAGGAATTCGTCAAT | 57695 |
rs585859 | snp | C/T | 0.499908 | 0.00678851 | intron-variant | USP37 | GRCh38.p7 | 2:218518398 | TGGTCCACTGCCGAT[C/T]TAAACTATTTCTTCT | 57695 |
rs586374 | snp | A/C | 0.447291 | 0.153545 | intron-variant | USP37 | GRCh38.p7 | 2:218518280 | CTGTGATAATTTCAC[A/C]GTTTAAGGTTTTCTA | 57695 |
rs588182 | snp | G/T | 0.388587 | 0.208071 | intron-variant | USP37 | GRCh38.p7 | 2:218547612 | ACTAGAGCCATGTCT[G/T]TGTGTGTCTTTTTTT | 57695 |
rs590771 | snp | C/T | 0.447291 | 0.153545 | intron-variant | USP37 | GRCh38.p7 | 2:218505128 | caagcaatcctccca[C/T]ctcagcctcccaagc | 57695 |
rs593888 | snp | A/G | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218562874 | AAATTAATACTTAAA[A/G]GAAAGTGGGCTGGGC | 57695 |
rs597301 | snp | A/G | 0.031825 | 0.122064 | intron-variant | USP37 | GRCh38.p7 | 2:218521947 | tggcgtgatcacagc[A/G]cactgcagcctcgac | 57695 |
rs598701 | snp | C/G | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218522282 | GAAATAGAATTTAAg[C/G]ctgagcacactggct | 57695 |
rs599973 | snp | C/G | 0.38821 | 0.208322 | intron-variant | USP37 | GRCh38.p7 | 2:218522550 | cctaggtgacagagg[C/G]aaactccaccacaaa | 57695 |
rs603585 | snp | C/T | 0 | 0 | intron-variant | USP37 | GRCh38.p7 | 2:218484321 | TTTATAAAGTCATTT[C/T]TTTAAAACCAACTTC | 57695 |
rs620049 | snp | A/G | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218507041 | gacctcaagtgatcc[A/G]cctgccttggcctcc | 57695 |
rs626432 | snp | A/C | 0.385932 | 0.209815 | intron-variant | USP37 | GRCh38.p7 | 2:218490935 | ctggagagcagtggc[A/C]cgaccacggctcact | 57695 |
rs630858 | snp | G/T | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218544966 | GTGCGGTCTTCTCTA[G/T]AAGGTCTAAATGTAC | 57695 |
rs632554 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | USP37 | GRCh38.p7 | 2:218544585 | GTTTTCTTTAAAGGC[C/T]ACCACCAAAATAGAT | 57695 |
rs634590 | snp | A/C | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218508045 | AGCACCCACAGGCTT[A/C]ACCAGTAGAAAACAG | 57695 |
rs635573 | snp | A/T | 0.031825 | 0.122064 | intron-variant | USP37 | GRCh38.p7 | 2:218512383 | gtagtggcgcacacc[A/T]gtagtccccagctac | 57695 |
rs636723 | snp | A/G | 0.387642 | 0.208697 | intron-variant | USP37 | GRCh38.p7 | 2:218508474 | AAGGCTCTCAAAAGA[A/G]TCTGAAGGAGGTGAA | 57695 |
rs639913 | snp | A/C | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218501248 | ttttgtcatgttacc[A/C]aggctggttttgaac | 57695 |
rs642520 | snp | A/G | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218558882 | AACCATACTGCTACC[A/G]CTAAAGACATGTCAA | 57695 |
rs642950 | snp | C/T | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218469913 | gcaacctctgcctcc[C/T]gggttcttgccattc | 57695 |
rs645796 | snp | A/G | 0.447162 | 0.153712 | intron-variant | USP37 | GRCh38.p7 | 2:218524513 | TATTTCTTTTGTCCA[A/G]TGTTTTATTAAGTAT | 57695 |
rs646295 | snp | G/T | 0.437965 | 0.164831 | intron-variant | USP37 | GRCh38.p7 | 2:218543835 | GAGCTATGTTTTTTT[G/T]tttgtttgttttttg | 57695 |
rs655441 | snp | C/T | 0.387453 | 0.208822 | intron-variant | USP37 | GRCh38.p7 | 2:218492822 | ctagactgggcaaca[C/T]agtgagagcccgtct | 57695 |
rs656862 | snp | A/C | 0.031825 | 0.122064 | intron-variant | USP37 | GRCh38.p7 | 2:218470650 | atgctccagtcatgc[A/C]gatcattctgaactt | 57695 |
rs659185 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | USP37 | GRCh38.p7 | 2:218471212 | TGGGGTTTTGTCAGG[C/T]TACTGCGACAGAAGA | 57695 |
rs660432 | snp | C/T | 0.499923 | 0.00618962 | upstream-variant-2KB, intron-variant | CNOT9, USP37 | GRCh38.p7 | 2:218567404 | CCACATCCATGGCTT[C/T]AATTACTATCAATAT | 57695 |
rs662250 | snp | A/T | 0.406123 | 0.195258 | intron-variant | USP37 | GRCh38.p7 | 2:218509394 | CGAAGATTTAAAATT[A/T]AAAAAAAATCAATTT | 57695 |
rs664514 | snp | A/G | 0.388021 | 0.208447 | intron-variant | USP37 | GRCh38.p7 | 2:218465096 | TAAATAAACAGGAAG[A/G]CAGATAAATGTTCTA | 57695 |
rs666546 | snp | A/T | 0.031825 | 0.122064 | intron-variant | USP37 | GRCh38.p7 | 2:218494122 | CACCAGGGGGAAAAG[A/T]CTGATGAAGTCCTGA | 57695 |
rs667251 | snp | C/G | 0.388021 | 0.208447 | intron-variant | USP37 | GRCh38.p7 | 2:218519661 | tttttttctgagaca[C/G]agtctccctctgtcc | 57695 |
rs670695 | snp | C/G | 0.499918 | 0.00638925 | intron-variant | USP37 | GRCh38.p7 | 2:218503535 | agcctgaccaatatg[C/G]agaaacctcgtctct | 57695 |
rs678218 | snp | A/C | 0.499923 | 0.00618962 | intron-variant | USP37 | GRCh38.p7 | 2:218514986 | ggctcctgtgtcttt[A/C]ggacatttcctcata | 57695 |
rs678814 | snp | A/G | 0.447032 | 0.153878 | intron-variant | USP37 | GRCh38.p7 | 2:218494564 | GCCCTATCATATCCT[A/G]TTACTCTGTGCCACT | 57695 |
rs681977 | snp | C/T | | | intron-variant | USP37 | GRCh38.p7 | 2:218503673 | tgagccgagatcgca[C/T]cgttgcactccagcc | 57695 |
rs684776 | snp | C/T | 0.387642 | 0.208697 | intron-variant | USP37 | GRCh38.p7 | 2:218459293 | TGCAACCTCCTCCTC[C/T]TCCCAGGTTCAGGTG | 57695 |
rs687747 | snp | A/G | 0.387832 | 0.208572 | intron-variant | USP37 | GRCh38.p7 | 2:218534904 | ATTGGCTCTTGAGAT[A/G]GTAATTAAAGATTAT | 57695 |
rs688116 | snp | A/G | 0.402454 | 0.198136 | intron-variant | USP37 | GRCh38.p7 | 2:218527031 | CCGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 57695 |
rs689116 | snp | A/C | 0.499859 | 0.0083854 | intron-variant, upstream-variant-2KB | CNOT9, USP37 | GRCh38.p7 | 2:218569165 | TATTTCCTTGCCGGA[A/C]GCCTCTCGCGGCCTT | 57695 |
rs711186 | snp | A/G | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218481379 | TATTGATTCCTAAGC[A/G]CCTATCTCAGACCTA | 57695 |
rs711190 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP37 | GRCh38.p7 | 2:218521202 | agaactgtgtgtcaa[C/T]taaacctcttttctt | 57695 |
rs711191 | snp | A/T | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218521361 | cctcaagttctggga[A/T]actgtacagaatgta | 57695 |
rs832802 | snp | C/T | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218522176 | AGTCACCACACCGCA[C/T]CAACATTAAGTCTTA | 57695 |
rs832804 | snp | C/T | 0.447421 | 0.153379 | intron-variant | USP37 | GRCh38.p7 | 2:218528086 | tgggcgctgtaatac[C/T]agctacttgggaggc | 57695 |
rs832808 | snp | C/T | 0.491525 | 0.0645418 | intron-variant | USP37 | GRCh38.p7 | 2:218543331 | tgtttttagtagaga[C/T]ggggtttcaccatgt | 57695 |
rs832810 | snp | A/G | 0.499923 | 0.00618962 | intron-variant | USP37 | GRCh38.p7 | 2:218457707 | GAATATCACTTTTTC[A/G]GTTTTGCTTTATTTT | 57695 |