| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs1464579 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185601858 | CTGAGGTCAGGAGTT[C/T]GAGACTGGCCTGGCC | 59343 |
| rs1464580 | snp | C/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185601742 | GCTGAGGTGGGAAAA[C/T]TGCTTGAACCCAGGA | 59343 |
| rs1568664 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | SENP2 | GRCh38.p7 | 3:185594443 | TGTGGCTAGTTCAAC[C/T]GAGGAACTGAATTTT | 59343 |
| rs1823238 | snp | A/G | 0.488424 | 0.0751925 | intron-variant | SENP2 | GRCh38.p7 | 3:185624182 | CCTCCCTCCCTGCAT[A/G]CTTTTAAAGTACACA | 59343 |
| rs2034343 | snp | A/T | 0.487368 | 0.0784625 | intron-variant | SENP2 | GRCh38.p7 | 3:185620066 | ctaaaaataaaaatt[A/T]aaaaaaaaaaaagaa | 59343 |
| rs2034344 | snp | A/G | 0.490007 | 0.0699769 | intron-variant | SENP2 | GRCh38.p7 | 3:185620000 | acacctgtaatacca[A/G]cactttgaaaaactg | 59343 |
| rs2121840 | snp | A/G | 0.396364 | 0.202676 | intron-variant | SENP2 | GRCh38.p7 | 3:185620296 | taaagccaggagctc[A/G]agactagcttgggca | 59343 |
| rs3087964 | snp | A/G | 0.469049 | 0.120489 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630614 | ACCACATTTCCAGAA[A/G]GGGAAGTCTCTTTAA | 59343 |
| rs4012716 | in-del | -/TT | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185601657 | TTTTTTTTTTTTTTT[-/TT]GAGATGGGGTCTTGC | 59343 |
| rs4267671 | snp | G/T | 0.272511 | 0.248984 | intron-variant | SENP2 | GRCh38.p7 | 3:185620209 | CTGGGACTACAGACA[G/T]GCACCACTATGCCTG | 59343 |
| rs4456898 | snp | A/G | 0.0236373 | 0.106113 | intron-variant | SENP2 | GRCh38.p7 | 3:185618466 | AGTCCCCTATGACTA[A/G]TTACTTATAAACACA | 59343 |
| rs4568175 | snp | C/T | 0.346811 | 0.230494 | intron-variant | SENP2 | GRCh38.p7 | 3:185618604 | CACCACTCGGCCGGG[C/T]GCGGTGGCTCACGCC | 59343 |
| rs4569690 | snp | C/T | 0.486 | 0.0824865 | intron-variant | SENP2 | GRCh38.p7 | 3:185618852 | CCAGTGGACTCCAGC[C/T]TGGGCGACAGGGCAA | 59343 |
| rs4624587 | snp | C/T | 0.396364 | 0.202676 | intron-variant | SENP2 | GRCh38.p7 | 3:185598828 | AGACCTAAGGTTTAA[C/T]TTGTCAAGACTCACA | 59343 |
| rs4686666 | snp | A/G | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185625059 | TCACACTTTTCTCTC[A/G]AGCCTAGCATCTCTC | 59343 |
| rs4686682 | snp | A/G | 0.372189 | 0.218105 | intron-variant | SENP2 | GRCh38.p7 | 3:185589614 | AGGCTTTTCACATGC[A/G]AAGACTTACTGCTAC | 59343 |
| rs4686683 | snp | A/C | 0.493432 | 0.0569306 | intron-variant | SENP2 | GRCh38.p7 | 3:185589575 | CTATTTGAGAGAGAA[A/C]CAAACTTCTTACCAA | 59343 |
| rs4686688 | snp | C/G | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185614889 | AAAGATCAATGTAGT[C/G]AAAGTGAATCAACAG | 59343 |
| rs4687477 | snp | A/G | 0.498323 | 0.0289051 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630563 | GAAGATGCTTGGATA[A/G]TCAGAGTCCCTTGGG | 59343 |
| rs4687523 | snp | C/G | 0.272511 | 0.248984 | intron-variant | SENP2 | GRCh38.p7 | 3:185607502 | TCTCTACTAAAAATA[C/G]AAAAAATTAGCCAGG | 59343 |
| rs4687533 | snp | A/G | 0.448452 | 0.152042 | intron-variant | SENP2 | GRCh38.p7 | 3:185596825 | ACTTTTACCACAGAG[A/G]TGAGGGCATGATTAA | 59343 |
| rs5855069 | in-del | -/A | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185624200 | AAGAAAGAAAAAAAA[-/A]GATGTGTACTTTAAA | 59343 |
| rs6444076 | snp | C/T | 0.372189 | 0.218105 | intron-variant | SENP2 | GRCh38.p7 | 3:185603617 | tcagagatatttgaa[C/T]acgggctacatatta | 59343 |
| rs6444077 | snp | C/G | 0.328148 | 0.237472 | intron-variant | SENP2 | GRCh38.p7 | 3:185603920 | tgaggccaggagttt[C/G]agaccagcctggcca | 59343 |
| rs6444078 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SENP2 | GRCh38.p7 | 3:185621371 | ATATAAGTGGATATC[A/G]TTTTTCTTttttttc | 59343 |
| rs6762208 | snp | A/C | 0.467773 | 0.122804 | missense | SENP2 | GRCh38.p7 | 3:185613377 | TTACTGATACAGAGA[A/C]GATGGTCGGAATCAG | 59343 |
| rs6764618 | snp | C/T | 0.482159 | 0.0927485 | intron-variant | SENP2 | GRCh38.p7 | 3:185610221 | GCTGGAGTGCAGTGA[C/T]GCAATCTCAGCTCAC | 59343 |
| rs6774871 | snp | A/G | 0.477515 | 0.103619 | intron-variant | SENP2 | GRCh38.p7 | 3:185629671 | TGTAAAAATGTCAAC[A/G]CTTAGAAAAAGCACA | 59343 |
| rs6776312 | snp | A/C | 0.486464 | 0.0811471 | intron-variant | SENP2 | GRCh38.p7 | 3:185587692 | ctgcctcagcctccc[A/C]agtagctgggactac | 59343 |
| rs6778977 | snp | G/T | 0.487241 | 0.0788465 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584744 | TTAGTAGAGATGGGG[G/T]TGTCTCACCATGTTG | 59343 |
| rs6783023 | snp | A/G | 0.372189 | 0.218105 | intron-variant | SENP2 | GRCh38.p7 | 3:185612401 | TATCACTCAGTTTAT[A/G]GTAAAGATTATATTT | 59343 |
| rs6784842 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185624935 | AGGAGAGCACAGATA[C/T]AAGGAAGAGTCTGTT | 59343 |
| rs6784948 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185624999 | AATAAAGAAAACAAA[C/T]TGCCTTTCTTTGTAT | 59343 |
| rs6785918 | snp | A/G | 0.484701 | 0.0861117 | intron-variant | SENP2 | GRCh38.p7 | 3:185612843 | TAGCCTGGTGGGTTG[A/G]GGGGGGTGCCCCTTA | 59343 |
| rs6791626 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SENP2 | GRCh38.p7 | 3:185602389 | cctgacagaggagga[G/T]atttcaaaggggctt | 59343 |
| rs6791954 | snp | C/T | 0.378765 | 0.214288 | intron-variant | SENP2 | GRCh38.p7 | 3:185617921 | TTAGGTGAATTCTTA[C/T]AGTAGCTATTTTTTT | 59343 |
| rs6795633 | snp | A/G | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185597957 | ccacaccagaccTAG[A/G]AAAGGATTATATTGA | 59343 |
| rs6799206 | snp | C/G | 0.47709 | 0.104548 | intron-variant | SENP2 | GRCh38.p7 | 3:185629442 | AATAAGCCGGGTGTG[C/G]TGGCACATACCTGTA | 59343 |
| rs6803426 | snp | A/G | 0.34659 | 0.230587 | intron-variant | SENP2 | GRCh38.p7 | 3:185618220 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGT | 59343 |
| rs6807777 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185606771 | GCCTATAGCGGCCAC[A/G]TGTGCTCAGTGAGTC | 59343 |
| rs6807879 | snp | A/T | 0.0267878 | 0.112589 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630004 | TGTACTCTAGTCCTG[A/T]CTTGGGGTGCAGAGG | 59343 |
| rs6807927 | snp | C/T | 0.375 | 0.216506 | intron-variant | SENP2 | GRCh38.p7 | 3:185607145 | AATTTCTCAGACTCC[C/T]TTCCATACCTGGCTT | 59343 |
| rs6807978 | snp | A/G | | | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630117 | TATTTTTTTTAAGAG[A/G]TTCTTTTCCCTATGA | 59343 |
| rs7374856 | snp | A/C | 0.48666 | 0.0805725 | intron-variant | SENP2 | GRCh38.p7 | 3:185594176 | TGGTTAAAAAAAAAA[A/C]ACACACACAAACGTT | 59343 |
| rs7615486 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | SENP2 | GRCh38.p7 | 3:185590707 | cccatctctactaaa[A/C]attaaaaaattagcc | 59343 |
| rs7644758 | snp | G/T | 0.486 | 0.0824865 | intron-variant | SENP2 | GRCh38.p7 | 3:185610409 | TCAGGTAGTCCACCA[G/T]CCTCAGCCTCCCAGA | 59343 |
| rs7646818 | snp | A/G | 0.328382 | 0.237395 | intron-variant | SENP2 | GRCh38.p7 | 3:185623728 | gctacttgggaggct[A/G]agtcaggagaatggc | 59343 |
| rs7648072 | snp | C/T | 0.486529 | 0.0809556 | intron-variant | SENP2 | GRCh38.p7 | 3:185626751 | gcactccagcctggg[C/T]gacagagcgagactc | 59343 |
| rs9714158 | snp | C/T | 0.486 | 0.0824865 | intron-variant | SENP2 | GRCh38.p7 | 3:185610992 | TTAAAGTTCCTGCTT[C/T]TGGCTGGGTGTGGTG | 59343 |
| rs9714159 | snp | A/G | 0.486332 | 0.08153 | intron-variant | SENP2 | GRCh38.p7 | 3:185610883 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 59343 |
| rs9758141 | snp | A/T | 0.372794 | 0.217765 | intron-variant | SENP2 | GRCh38.p7 | 3:185597297 | TTTTATTTAAAAAAC[A/T]CAATTACAATACTGG | 59343 |
| rs9833463 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | SENP2 | GRCh38.p7 | 3:185628599 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCAAGTC | 59343 |
| rs9835057 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185623610 | aggcgggatcacagg[C/T]tcaggagatcgagac | 59343 |
| rs9839326 | snp | A/G | 0.00629291 | 0.0557392 | intron-variant | SENP2 | GRCh38.p7 | 3:185629755 | ATTAATATGTAATGC[A/G]GGCGTTGTTTATGGG | 59343 |
| rs9866548 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | SENP2 | GRCh38.p7 | 3:185598044 | CAGAGACAGAGTCTC[A/T]CTCTGTTGCCCAGGC | 59343 |
| rs10553127 | in-del | -/AT | 0.34659 | 0.230587 | intron-variant | SENP2 | GRCh38.p7 | 3:185621252 | AAAAAAAAAAGTCTC[-/AT]CACTCTGAGAGGACC | 59343 |
| rs10715399 | in-del | -/T | 0.493523 | 0.0565391 | intron-variant | SENP2 | GRCh38.p7 | 3:185606987 | ATATTTCTTTTTTCC[-/T]TTTTTTTTTTTGAGA | 59343 |
| rs10937221 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584510 | atacacacatacaca[C/T]acacacacacacata | 59343 |
| rs10937222 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584524 | acacacacacacaca[C/T]acacacacacaTGTA | 59343 |
| rs10937223 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584528 | acacacacacataca[C/T]acacacaTGTAttta | 59343 |
| rs10937224 | snp | A/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584547 | cacaTGTAtttattt[A/T]atttatttatttttt | 59343 |
| rs10937225 | snp | A/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584548 | acaTGTAtttatttt[A/T]tttatttattttttg | 59343 |
| rs10937226 | snp | A/G | 0.487432 | 0.0782705 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585097 | TTTTTGATGGGGTGC[A/G]TCAGGGTCCCACTCT | 59343 |
| rs11315344 | in-del | -/T | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185601061 | TTTTTTTTTTTTTTT[-/T]GCGATGGAGTTTTGC | 59343 |
| rs11317593 | in-del | -/T | 0.488424 | 0.0751925 | intron-variant | SENP2 | GRCh38.p7 | 3:185594637 | TTTTTTTTTTTTTTT[-/T]GGGACAGAGTCTCGC | 59343 |
| rs11345567 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589086 | TTCATTTTTTTTTTT[-/T]GCATGTGTGAATATA | 59343 |
| rs11388775 | in-del | -/A/AA | 0.625 | 0.125 | intron-variant | SENP2 | GRCh38.p7 | 3:185621332 | CTAAAAAAAAAAAAA[-/A/AA]TACATGTACCAATAT | 59343 |
| rs11916386 | snp | G/T | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185590281 | AAGTCTTGGCCGGGC[G/T]CAGTGGCTGTAATCC | 59343 |
| rs11922634 | snp | A/G | 0.473818 | 0.111381 | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631402 | GGTGATGACTGAAGC[A/G]GGAGCAGGTTGTACC | 59343 |
| rs11924016 | snp | A/T | 0.482683 | 0.0914256 | intron-variant | SENP2 | GRCh38.p7 | 3:185590091 | AATCTATATATATAT[A/T]TTTTTTTCTTTCTCT | 59343 |
| rs11926948 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SENP2 | GRCh38.p7 | 3:185605054 | ccaccgcgcctggcc[A/G]aatctgtttatttct | 59343 |
| rs12374077 | snp | C/G | 0.486725 | 0.0803809 | intron-variant | SENP2 | GRCh38.p7 | 3:185599886 | GCGATCTCGGCTCCA[C/G]CTCCTGGGTTCAAGT | 59343 |
| rs12374078 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185600011 | CGTGTTGGTCAGGCT[A/G]GTCTTGAACTCCCGA | 59343 |
| rs12489330 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605262 | tgtaaccccagctac[A/T]cgggaggctgaggca | 59343 |
| rs12490885 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584518 | atacacacacacaca[C/T]acacatacacacaca | 59343 |
| rs12491310 | snp | C/G | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185600238 | TAGATTTGTGCCTGA[C/G]ATGCTGGCACTACTG | 59343 |
| rs12495848 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605266 | accccagctacacgg[C/G]aggctgaggcaggag | 59343 |
| rs13061708 | snp | C/T | 0.372391 | 0.217992 | intron-variant | SENP2 | GRCh38.p7 | 3:185622196 | AATGTTCTTAGGAAC[C/T]GTTAGTTGGGGAGTG | 59343 |
| rs13069058 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602937 | tttttttttgggatg[A/G]agtcttgctctgtca | 59343 |
| rs13072061 | snp | G/T | 0.486529 | 0.0809556 | intron-variant | SENP2 | GRCh38.p7 | 3:185608235 | ATATCCCTGAAAGGG[G/T]TTTTAAGATGAGGTG | 59343 |
| rs13072759 | snp | A/G | 0.486 | 0.0824865 | intron-variant | SENP2 | GRCh38.p7 | 3:185608603 | CTGAATCTTTAACCT[A/G]TTGGTGTTATTTAAA | 59343 |
| rs13076556 | snp | A/G | 0.373804 | 0.217192 | intron-variant | SENP2 | GRCh38.p7 | 3:185621787 | TCTCACTCCTCTTAC[A/G]TTTAAGATGTTTCTG | 59343 |
| rs13080101 | snp | C/T | 0.372794 | 0.217765 | intron-variant | SENP2 | GRCh38.p7 | 3:185625378 | TGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 59343 |
| rs13080779 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604844 | ccctgcaacctccgc[C/G]tcctgggttcgagca | 59343 |
| rs13080780 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604847 | tgcaacctccgcctc[C/T]tgggttcgagcaatt | 59343 |
| rs13081203 | snp | A/G | 0.486 | 0.0824865 | intron-variant | SENP2 | GRCh38.p7 | 3:185604855 | ccgcctcctgggttc[A/G]agcaattctcctgcc | 59343 |
| rs13091418 | snp | C/G | 0.486 | 0.0824865 | intron-variant | SENP2 | GRCh38.p7 | 3:185611968 | TCAAGACCAGCCTGG[C/G]GAACATGGTAAAACC | 59343 |
| rs13092283 | snp | C/T | 0.375 | 0.216506 | intron-variant | SENP2 | GRCh38.p7 | 3:185620217 | acagacatgcaccac[C/T]atgcctggctaattt | 59343 |
| rs13095912 | snp | A/G | 0.486133 | 0.082104 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584310 | GGGAATAAGGGAGGC[A/G]GGTGTGTCCACACTT | 59343 |
| rs13099996 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592008 | TAAGAACCGGTAATA[A/T]ttctttttttttttt | 59343 |
| rs13100034 | snp | A/G | 0.486529 | 0.0809556 | intron-variant | SENP2 | GRCh38.p7 | 3:185601016 | AGACTTGAACTTAGG[A/G]GTGTGTTATATTTTC | 59343 |
| rs13100229 | snp | C/T | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185625412 | CACCGTACCCGGCCA[C/T]TAGGCAAACTTTAAA | 59343 |
| rs13315419 | snp | A/C | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185602556 | taaaattagaaaatc[A/C]ccattttgtaactgt | 59343 |
| rs13340181 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | SENP2 | GRCh38.p7 | 3:185607824 | AGCCACCGCGTCCAG[C/T]CATAACTTGTTTCTT | 59343 |
| rs17523471 | snp | A/G | 0.488786 | 0.0740357 | upstream-variant-2KB, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586230 | CCCCCGCCCGCCACC[A/G]CTCCTGACGTCACCT | 59343 |
| rs28420311 | snp | C/G | | | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598543 | GTGGCCCCTTCAGGA[C/G]AGGTCAGTGGGGATG | 59343 |
| rs28616682 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612019 | AAAATTAGCCAGGCA[C/T]GGTGGCACTTGCCTG | 59343 |
| rs28628232 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185625812 | TGGCCCTTTTTAAAA[A/T]TGATAAATGCTTCTG | 59343 |
| rs34162716 | snp | A/C | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185614799 | ATAACCTCAGTTATT[A/C]TAACTTGAATGTTTT | 59343 |
| rs34288538 | in-del | -/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185626101 | AGGCCTGTTTTTCCC[-/C]TTGCTATGATCTATG | 59343 |
| rs34321126 | in-del | -/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607853 | TTTTTATAAACTTTA[-/G]TAACTGTGACTAAGG | 59343 |
| rs34398323 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185625603 | GTTAGAATCCACCAC[C/T]TTTGGCTTATTATGC | 59343 |
| rs34406883 | in-del | -/AA | | | intron-variant | SENP2 | GRCh38.p7 | 3:185627107 | AAAAAAAAAAAAAAA[-/AA]TAGTAGTAGCTGTGC | 59343 |
| rs34475616 | in-del | -/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589935 | GCCTCCCAAAGTGCT[-/G]GGGATTACAGGCACG | 59343 |
| rs34505819 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | SENP2 | GRCh38.p7 | 3:185622933 | GTGATGCTCGTTCCT[C/T]GGCCTCCCAAGAAGC | 59343 |
| rs34619288 | snp | C/G | 0.346811 | 0.230494 | intron-variant | SENP2 | GRCh38.p7 | 3:185613890 | TTTTTTCTTCCTTCT[C/G]AGTTGTTGGAGTTTT | 59343 |
| rs34621498 | snp | A/C | | | missense | SENP2 | GRCh38.p7 | 3:185609275 | AGGAAAGAGAGAAGT[A/C]CCGAAAGTTATTGGA | 59343 |
| rs34696239 | in-del | -/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589284 | TTTTTTAAGTTGTAG[-/C]AACAGTTTTTTTTAA | 59343 |
| rs34765114 | snp | A/T | 0.484771 | 0.0859212 | intron-variant | SENP2 | GRCh38.p7 | 3:185617368 | GATAGTATATTTTTC[A/T]CAAGAGTCAGGTGTT | 59343 |
| rs34843707 | in-del | -/A/AA | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629590 | GCAAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAG | 59343 |
| rs34862744 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596318 | GTTCTATCTTAGATG[C/T]TTAAAAGCTGCATAT | 59343 |
| rs34897313 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616776 | GAGACTCCGTCTCCA[-/A]AAAAAAAAAAAAAAC | 59343 |
| rs34907174 | in-del | -/T | 0.491834 | 0.0633738 | intron-variant | SENP2 | GRCh38.p7 | 3:185592620 | TAAGACAGGGTCTCC[-/T]TTTTTTTTTTTTTTG | 59343 |
| rs34965813 | snp | C/T | 0.486529 | 0.0809556 | intron-variant | SENP2 | GRCh38.p7 | 3:185615224 | TGGCTTCCTCCACAA[C/T]GTTGCCCTAGTAGGC | 59343 |
| rs35067768 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185623115 | AGCCACCGTGCCCGG[G/T]GGTCTTTGGCTTTTT | 59343 |
| rs35161796 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185605762 | TTGCATTGTTGGTAA[G/T]GGCAGGAAAGGCAGA | 59343 |
| rs35242554 | in-del | -/ATTT | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584556 | ACATGTATTTATTTT[-/ATTT]ATTTATTTTTTGAGA | 59343 |
| rs35308544 | in-del | -/A | 0.397271 | 0.202018 | intron-variant | SENP2 | GRCh38.p7 | 3:185616871 | TGGGTTCAAATCTTC[-/A]TTCTACCTTTTAATA | 59343 |
| rs35497918 | snp | C/T | 0.48666 | 0.0805725 | intron-variant | SENP2 | GRCh38.p7 | 3:185592524 | TTTGTGTTAATATTT[C/T]GTTTAAATTCAGTGA | 59343 |
| rs35544257 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185599981 | TTTGTATTTTTAGTA[A/G]AGACTGGGTTTCTCC | 59343 |
| rs35589727 | snp | A/G | 0.0266618 | 0.112339 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598532 | ACCTCTCCTGAAGGG[A/G]CCACATTCCGTGTTC | 59343 |
| rs35598169 | snp | A/G | 0.431325 | 0.172108 | intron-variant | SENP2 | GRCh38.p7 | 3:185628632 | CCGCTTCAGCCTCCC[A/G]AGTAACCGTGATTAC | 59343 |
| rs35637544 | snp | A/G | 0.370974 | 0.218781 | intron-variant | SENP2 | GRCh38.p7 | 3:185612170 | AAAAAAAAAAAAAAA[A/G]CCTCACAGCATTGAC | 59343 |
| rs35709607 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589231 | TGTAGTTTGCGTGAT[-/A]AAAATGAAGTTAAAT | 59343 |
| rs35711486 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622841 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAT | 59343 |
| rs35712770 | in-del | -/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185593371 | TCTCACCTTGGCTTT[-/G]CCAAAATGTTGGGAT | 59343 |
| rs35811347 | in-del | -/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592741 | CTGCCTCAGCTTCCC[-/C]AAGTAGCTGGGACTA | 59343 |
| rs35853080 | snp | A/C | 0.47709 | 0.104548 | intron-variant | SENP2 | GRCh38.p7 | 3:185628926 | CAGTTAAAGCAGAAT[A/C]ATTTATTAAGCAAAA | 59343 |
| rs35917986 | snp | A/G | 0.48679 | 0.0801892 | intron-variant | SENP2 | GRCh38.p7 | 3:185592253 | CTGGCAAATTATTTT[A/G]TATGTGGATACTGAG | 59343 |
| rs36066570 | snp | A/C | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185596666 | CTTTACTTAGCCAAG[A/C]TATAATACGGGCTTA | 59343 |
| rs55897322 | in-del | -/AA | | | intron-variant | SENP2 | GRCh38.p7 | 3:185624878 | CTCAAAAAAAAAAAA[-/AA]GAAAAAGAAAAATTT | 59343 |
| rs55993776 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584474 | ATATATATATATATA[C/T]ATATATATATATATA | 59343 |
| rs56021904 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622325 | TGAGGAGACTGTTTC[A/C]AATAGTAATTGCTAT | 59343 |
| rs56147684 | in-del | -/TATATATATATATATATATATA | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584474 | ATATATATATATATA[-/TATATATATATATATATATATA]TACACACATACACAC | 59343 |
| rs56239593 | in-del | -/TATATATATATATATATATATA | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584476 | ATATATATATATATA[-/TATATATATATATATATATATA]CACACATACACACAC | 59343 |
| rs56257241 | snp | C/T | 0.267636 | 0.249377 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584496 | ATATATATATATATA[C/T]ACACACATACACACA | 59343 |
| rs56668026 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602667 | CGAGAAATCCCGTTT[C/T]TACTAAAAATAGAAA | 59343 |
| rs56856415 | snp | C/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185615406 | TGGAGTGCAATGGCG[C/T]GATCTTGGCTCACTG | 59343 |
| rs56898540 | in-del | -/CACA | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584523 | ACACACACACACACA[-/CACA]TACACACACACATGT | 59343 |
| rs57105387 | in-del | -/TATATA | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584492 | ATATATATATATATA[-/TATATA]CACACATACACACAC | 59343 |
| rs57175227 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596385 | AGCACTTTGGGAGGC[A/T]GAGGCAGAAGGATCA | 59343 |
| rs57304676 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607212 | ATACCTATATGTATT[C/T]TTCTATAGATATTCT | 59343 |
| rs58192571 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185613848 | AAAAAAAAAAAAAAA[-/A]GGCAGGAAGCATTGA | 59343 |
| rs59082903 | snp | C/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185603158 | CTCAGGTGATCCAAC[C/T]GCCTCGGCCTCCCAA | 59343 |
| rs59366743 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622063 | GCTGATTTCAACTGA[A/G]AAAACGTGTTTAGTA | 59343 |
| rs59565990 | in-del | -/TTTTTTTTT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185587752 | TTTTTTTTTTTTTTT[-/TTTTTTTTT]GAGACAGAGTCTCAT | 59343 |
| rs59712448 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596558 | CCTGGGAGGTTGAGG[C/T]TGCAGTGAGTAGTGA | 59343 |
| rs59727746 | in-del | -/TATA | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584497 | ATATATATATATATA[-/TATA]CACACATACACACAC | 59343 |
| rs59926388 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185608673 | TGCAAGAAGAGATAC[A/G]GGCAAACCATCAGTA | 59343 |
| rs60252560 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602089 | TCTTTCCTTATCTCT[C/T]TAAAGCTGTTTATTA | 59343 |
| rs60397567 | in-del | -/C | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185608281 | TCTTAGATGAGAAAT[-/C]AGAAATGGGACTGAG | 59343 |
| rs60566929 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605203 | GGTGAAACCCCATCT[C/T]TACTTAAAATACAAA | 59343 |
| rs60937881 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SENP2 | GRCh38.p7 | 3:185627523 | GTTCAAGCAATACTC[C/T]TGCCTCAGCCTCCCC | 59343 |
| rs61253950 | in-del | -/CACT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185586829 | GTCTTTGTTGTGGCT[-/CACT]GTTTACAAAGCACCC | 59343 |
| rs61396369 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596418 | TGAGCCCAGGAGTTC[A/C]AGACCAGCCTGGGCA | 59343 |
| rs62289068 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604053 | TTCAACCCGGAAGGC[A/G]GAGGTTGTAATGAGC | 59343 |
| rs62289069 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | SENP2 | GRCh38.p7 | 3:185606901 | AACTTTTTTCAGAAA[A/T]AAAAATTAAAAGACT | 59343 |
| rs62291879 | snp | A/G | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185587317 | TTTGTGTTTTTAGTA[A/G]AGATGGGGTTTCACT | 59343 |
| rs62291881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185593409 | GTGAACCACCATCCC[C/T]GGCCAAGGATTTTCA | 59343 |
| rs62291882 | snp | C/T | 0.375399 | 0.216275 | intron-variant | SENP2 | GRCh38.p7 | 3:185595490 | TGCTTTACCTGGCCA[C/T]TACTTTTTCCCTTTT | 59343 |
| rs62291883 | snp | C/T | 0.380529 | 0.213219 | intron-variant | SENP2 | GRCh38.p7 | 3:185596054 | CACTGCAACCTCCGC[C/T]TCCTGGATTCAAACG | 59343 |
| rs62291884 | snp | A/G | 0.486595 | 0.0807641 | intron-variant | SENP2 | GRCh38.p7 | 3:185596067 | GCTTCCTGGATTCAA[A/G]CGATTCTGCTGCCTC | 59343 |
| rs62842660 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616872 | GGGTTCAAATCTTCT[-/A]TCTACCTTTTAATAA | 59343 |
| rs62877061 | in-del | -/TGA | 0.486133 | 0.082104 | intron-variant | SENP2 | GRCh38.p7 | 3:185612517 | TGTAGAGGAATGTCT[-/TGA]TGTTGTGGAAACTCT | 59343 |
| rs62894960 | in-del | -/A | 0.375 | 0.216506 | intron-variant | SENP2 | GRCh38.p7 | 3:185596621 | GTAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAG | 59343 |
| rs63047860 | in-del | -/T | 0.416871 | 0.186156 | intron-variant | SENP2 | GRCh38.p7 | 3:185599826 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 59343 |
| rs63132560 | in-del | -/CA | 0 | 0 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584516 | ACACACACACACACA[-/CA]TACACACACACATGT | 59343 |
| rs63406860 | in-del | -/CTCA | 0.0322114 | 0.122752 | intron-variant | SENP2 | GRCh38.p7 | 3:185586827 | CTGTCTTTGTTGTGG[-/CTCA]CTGTTTACAAAGCAC | 59343 |
| rs63575061 | in-del | -/CT | 0.371785 | 0.218331 | intron-variant | SENP2 | GRCh38.p7 | 3:185623224 | TCGGCTCACCGCAAC[-/CT]CTGTCTCCCGGGTTC | 59343 |
| rs63707460 | in-del | -/AAAAA | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185623827 | AAAAAAAAAAAAAAA[-/AAAAA]TCCAGAAAGCAGTCA | 59343 |
| rs71320310 | snp | C/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185591846 | AGGTGATCCTTCCAT[C/T]TCAGCCTCCCAAGTA | 59343 |
| rs71320311 | snp | A/G | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185621574 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCGCC | 59343 |
| rs71320312 | snp | A/G | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185624825 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 59343 |
| rs71631266 | snp | C/T | 0 | 0 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584502 | ATATATATATACACA[C/T]ATACACACACACACA | 59343 |
| rs71631267 | snp | C/T | 0 | 0 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584504 | ATATATATACACACA[C/T]ACACACACACACACA | 59343 |
| rs71632072 | in-del | -/C | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185610931 | CACTGCACTCCAGCC[-/C]TGAGCTACAGATCGA | 59343 |
| rs73056896 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SENP2 | GRCh38.p7 | 3:185611322 | TTGTTTCAGGATCCA[C/T]TTAAATACATAGCTT | 59343 |
| rs73058823 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185625623 | GCTTATTATGCTCTT[A/C]GTGCTGCTTGTACCA | 59343 |
| rs73175547 | snp | C/T | 0.13339 | 0.221138 | intron-variant | SENP2 | GRCh38.p7 | 3:185609224 | TGTGCTGGTACTTAT[C/T]TAACATGCTTTCTTT | 59343 |
| rs73175548 | snp | C/T | 0.186105 | 0.241697 | intron-variant | SENP2 | GRCh38.p7 | 3:185612515 | AATGTAGAGGAATGT[C/T]TTGATGTTGTGGAAA | 59343 |
| rs73175550 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185619737 | TTATTTTACTATTTT[C/T]TAAAATTACAGACCA | 59343 |
| rs73885751 | snp | A/G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185586038 | GGCCTTGTCCCACGG[A/G/T]CCGGCTCCGGATTGG | 59343 |
| rs74211200 | snp | A/G | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185595990 | ATTTATTTTGAGATG[A/G]AGTCTCACGCTGTTG | 59343 |
| rs74286276 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185595230 | TTATGATATTGTTTA[A/G]TAGCCACARTTTGCT | 59343 |
| rs74336964 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185605747 | CATGATGTCAGTTTG[C/T]TGCATTGTTGGTAAT | 59343 |
| rs74430300 | snp | A/G | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185612268 | GATTATTATTCCTAA[A/G]CTGCTAGATAGTAGC | 59343 |
| rs74466592 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185598335 | TAAAAATTGAGAGAG[A/G]CTCTTTCCAAGATAT | 59343 |
| rs74496415 | snp | C/T | 0.185155 | 0.241444 | intron-variant | SENP2 | GRCh38.p7 | 3:185596821 | TTGTTTAATCATGCC[C/T]TCACCTCTGTGGTAA | 59343 |
| rs74568138 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SENP2 | GRCh38.p7 | 3:185627841 | CAACCTCATTAAAGA[A/G]TATTTTTCATCCACA | 59343 |
| rs74664153 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185599496 | TTGTCATTATTATAT[A/G]TATGCACTATACAAA | 59343 |
| rs74704545 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SENP2 | GRCh38.p7 | 3:185619620 | ATATTATAAGCATAC[C/T]CTGCAGAGTCTCTTT | 59343 |
| rs74705076 | snp | C/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185591597 | ACTTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 59343 |
| rs74799677 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SENP2 | GRCh38.p7 | 3:185625676 | ACTGATCCATCAAGG[C/T]AAGATCCTAATTGGT | 59343 |
| rs74864314 | snp | G/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185592632 | TCCTTTTTTTTTTTT[G/T]TTGAGATGGAGTCTT | 59343 |
| rs74950171 | snp | G/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185593746 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTCTTT | 59343 |
| rs75020582 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SENP2 | GRCh38.p7 | 3:185589773 | TCCTGGGCTCAAGTG[A/T]TCCTCCTGCCTTAGT | 59343 |
| rs75353873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185619899 | TGCTTGCCTAATTTT[A/G]TTTATTTATATATTT | 59343 |
| rs75369345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185588859 | AGCTAATTTCCTCTC[C/T]CTTGTCCTCTCCTTG | 59343 |
| rs75374456 | snp | C/T | 0.272511 | 0.248984 | intron-variant | SENP2 | GRCh38.p7 | 3:185622684 | TGTGTATAAATTGTG[C/T]GCACATACATTTGCA | 59343 |
| rs75403119 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612519 | TAGAGGAATGTCTTG[A/T]TGTTGTGGAAACTCT | 59343 |
| rs75457670 | snp | C/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185598768 | CATATGCTTTCTTAT[C/T]TAAGGATGTACAAAG | 59343 |
| rs75499727 | snp | A/C/T | 0.0225045 | 0.103662 | intron-variant | SENP2 | GRCh38.p7 | 3:185613085 | TTCTATTGGAACATG[A/C/T]GAATTCATTTACATA | 59343 |
| rs75503055 | snp | C/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185592011 | GAACCGGTAATATTT[C/T]TTTTTTTTTTTTTTT | 59343 |
| rs75722837 | snp | G/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185593745 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTTTCTT | 59343 |
| rs75841015 | snp | C/T | 0.00176467 | 0.0296517 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185624082 | CAGCATGAAACCACA[C/T]GTGAGTGACGATCAT | 59343 |
| rs76010631 | snp | A/G | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185611485 | TAGAATCATGATTAG[A/G]CTCCTTTTATCCTAG | 59343 |
| rs76029614 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185605377 | ACTTCGTCGAAAAAA[A/G]AAAGAATAAGGGCAT | 59343 |
| rs76152458 | snp | C/T | 0.040671 | 0.13668 | intron-variant | SENP2 | GRCh38.p7 | 3:185589303 | AGTTTTTTTTAACTC[C/T]CTTACACACACACAA | 59343 |
| rs76181270 | in-del | -/TT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185593729 | TTGTGTTTTCATTTC[-/TT]TTTTTTTTTTTTTTT | 59343 |
| rs76195891 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185617889 | AAACGGGAGGAAGCA[A/G]CAAGTGATACTGTAT | 59343 |
| rs76247522 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185608181 | CGAGCTTATACATAA[A/G]TAGTTGCTATTTGAT | 59343 |
| rs76275277 | snp | G/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185605676 | CCTTTTTTTTTTTTT[G/T]TGAAACACCACATAA | 59343 |
| rs76350357 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SENP2 | GRCh38.p7 | 3:185626234 | ATATTTAGAAAAAGT[C/T]CAAGGAATTTGTATT | 59343 |
| rs76602743 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | SENP2 | GRCh38.p7 | 3:185624800 | CCTCATTGCAACCTC[C/T]GCCTCTTAGGTTCAA | 59343 |
| rs76614936 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | SENP2 | GRCh38.p7 | 3:185608898 | GAAACTGTATATTCT[C/T]GTTATGCAAGCAGAT | 59343 |
| rs76764785 | snp | G/T | 0.030665 | 0.119967 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630181 | TTTGTTTCTGTGTGT[G/T]TGTTCAGCGTATTCA | 59343 |
| rs76893815 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612209 | ATCTAGGAATTTAGT[-/A]GAAAAGCTGTTTCAG | 59343 |
| rs76990827 | snp | C/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185601066 | TTTTTTTTTTTGCGA[C/T]GGAGTTTTGCTCTGT | 59343 |
| rs77086556 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185606216 | GTACTTGTCTGACTT[G/T]CCAGGAGTAAGCTTG | 59343 |
| rs77143484 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185601018 | ACTTGAACTTAGGGG[C/T]GTGTTATATTTTCTT | 59343 |
| rs77241377 | snp | C/T | 0 | 0 | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631450 | CTCCCACTCCCCCTC[C/T]CTCCCTCTCCCCTCC | 59343 |
| rs77636274 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | SENP2 | GRCh38.p7 | 3:185614174 | ATAAACTAGAACCAA[C/G]TTGAGTTACTATAAA | 59343 |
| rs77707823 | snp | A/C | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185618879 | GCAAGACTCCGTCTC[A/C]AAAAAAAAGTATCAC | 59343 |
| rs77720112 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SENP2 | GRCh38.p7 | 3:185612949 | TCAGTGTCTTTAGGA[C/T]AGGAACAGTAAAGGC | 59343 |
| rs77780164 | snp | G/T | 0.444444 | 0.157135 | intron-variant | SENP2 | GRCh38.p7 | 3:185624804 | ACCTGGGAGGCGGAG[G/T]TTGCAGTGAGCAGAG | 59343 |
| rs77972268 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185624444 | CATGTCTCTCACAGA[A/T]TTGGGAAGAAACCCA | 59343 |
| rs77975449 | snp | C/T | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185596176 | GCCATGATGGTCAGG[C/T]TGGTCTTGAACTCCT | 59343 |
| rs78013191 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | SENP2 | GRCh38.p7 | 3:185625439 | TAAAAATCATAATCA[A/T]CTTCATTTCTTTGAG | 59343 |
| rs78099728 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185599758 | GGAGAATAAATACAT[-/T]ACCCCTGTGTCTGAG | 59343 |
| rs78192861 | snp | G/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185593744 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTTTCT | 59343 |
| rs78263789 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185589407 | CTTTCTTTGGGGATC[A/G]TTTTCAAAAGGAAAT | 59343 |
| rs78266569 | snp | G/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185595032 | CCTGGCTCAGGCTCA[G/T]GACCTTAAAGGTGAA | 59343 |
| rs78336354 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185627956 | AGTAACTAGGACTCC[C/T]GTGCTGAATTAATAT | 59343 |
| rs78433671 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185595239 | TGTTTAGTAGCCACA[A/G]TTTGCTATGTTACCA | 59343 |
| rs78506856 | in-del | -/TT | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185611365 | ATCTTTTAATCTGAG[-/TT]TTATCACACTGAGAT | 59343 |
| rs78517459 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185604431 | AATGACCTAAATGTC[A/G]GGTCAGGTTGGTTGA | 59343 |
| rs78627355 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185593624 | TATTTCACACAGAAA[A/G]TCTTGATTTAATGCT | 59343 |
| rs78830864 | snp | A/T | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185627108 | AAAAAAAAAAAAAAA[A/T]AGTAGTAGCTGTGCT | 59343 |
| rs78873116 | snp | C/T | 0.117537 | 0.212022 | intron-variant | SENP2 | GRCh38.p7 | 3:185599080 | TCTGCCCATTTTTTT[C/T]CTACATTTTGAAAAT | 59343 |
| rs79135575 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185623440 | CACCGCACCCGGCCT[A/G]TGTTATTTTTTGTAT | 59343 |
| rs79179434 | snp | A/G | 0.269809 | 0.249214 | intron-variant | SENP2 | GRCh38.p7 | 3:185617267 | GCCCAGGAGTTTGCA[A/G]CCAACTTGGGCAATA | 59343 |
| rs79193891 | snp | A/C/G | 0.00151651 | 0.027495 | missense | SENP2 | GRCh38.p7 | 3:185609340 | TGTCCTGTAACTTCA[A/C/G]ATTATCACAGGTGAC | 59343 |
| rs79328132 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SENP2 | GRCh38.p7 | 3:185607877 | ACTAAGGAAGGGAAG[G/T]AAATGGTGTGCATCT | 59343 |
| rs79378867 | snp | A/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185624864 | CAGAGCGAGACTGTC[A/T]CAAAAAAAAAAAAAA | 59343 |
| rs79488427 | in-del | -/CT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185593728 | ATTGTGTTTTCATTT[-/CT]TTTTTTTTTTTTTTT | 59343 |
| rs79520266 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185629717 | ATTACATGATTACAC[C/G]TGAAGGTTGTGCTGC | 59343 |
| rs79523219 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SENP2 | GRCh38.p7 | 3:185602785 | GTGCAGTGAGCTAAG[A/T]TTACACCACTGCACT | 59343 |
| rs79571550 | snp | A/G | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185613848 | AAAAAAAAAAAAAAA[A/G]GGCAGGAAGCATTGA | 59343 |
| rs79658417 | snp | C/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185624798 | TCACTGCAAGCTCCG[C/T]CTCCTGGGTTCACAC | 59343 |
| rs79756960 | snp | G/T | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185625128 | ATTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 59343 |
| rs79811157 | snp | A/G | 0.0581099 | 0.160244 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585055 | TCTATCACTAAATAG[A/G]GTGGGATTTGTTTTA | 59343 |
| rs79852235 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SENP2 | GRCh38.p7 | 3:185597252 | TATGGATTTGCTAAA[A/G]TGATGGTTTTATGTT | 59343 |
| rs80053091 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SENP2 | GRCh38.p7 | 3:185622685 | GTGTATAAATTGTGC[A/G]CACATACATTTGCAT | 59343 |
| rs80062265 | snp | G/T | 0.0558544 | 0.157504 | intron-variant | SENP2 | GRCh38.p7 | 3:185614250 | TTTGCTGTTTAAAAC[G/T]TTCATAATATCTTTT | 59343 |
| rs80164709 | snp | A/G | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185613991 | TTATGGCTTCTTAGG[A/G]AGAATTTCTTAAAAA | 59343 |
| rs80286341 | snp | C/T | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185624812 | GGCGTGATCTCGGCT[C/T]ACTGCAACCTCTGCC | 59343 |
| rs111307985 | snp | A/G | 0.273049 | 0.248935 | intron-variant | SENP2 | GRCh38.p7 | 3:185591035 | TCAGCCTCCCGAGTA[A/G]CTGGGATTACAGGCA | 59343 |
| rs111334715 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616711 | CCCCGGGAGGCGGAG[C/G]TTGCAGTAAGCCGAG | 59343 |
| rs111437244 | in-del | -/CTGCACT | 0.486529 | 0.0809556 | intron-variant | SENP2 | GRCh38.p7 | 3:185590822 | GCCAAGAATCTGCTA[-/CTGCACT]CTGCACTCCAGCCTG | 59343 |
| rs111472562 | snp | C/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185629687 | CTTAGAAAAAGCACA[C/T]GGACATCCTGCTTTA | 59343 |
| rs111526894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185629345 | ACTTTGGGATGCTGA[A/G]GCGGGCGGATCACCT | 59343 |
| rs111572037 | snp | C/T | 0.185472 | 0.241529 | intron-variant | SENP2 | GRCh38.p7 | 3:185597455 | CCTCCCAGGTTCCAG[C/T]GATTCTCCTGCATCA | 59343 |
| rs111634964 | snp | A/C | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185612709 | ATATATATTTTCTTA[A/C]TTTATAAGCTGTATT | 59343 |
| rs111753200 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185622895 | AGTCTCAGCTCACTG[C/T]AACCTCTGCCTCCTG | 59343 |
| rs111809814 | snp | C/T | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185621391 | TCTTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 59343 |
| rs111970647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185613206 | TTTTCAGAAAAGTTC[A/G]TTGACTCCTGGTTTA | 59343 |
| rs111976837 | snp | A/G | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185601179 | CTCCTGAGTAGCTGG[A/G]ATTACAGGCACCCCC | 59343 |
| rs112006815 | snp | A/G | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185629686 | ACTTAGAAAAAGCAC[A/G]TGGACATCCTGCTTT | 59343 |
| rs112033729 | snp | A/G | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185612456 | TTTTTAGGCAACTTA[A/G]TATATAGGGAGGCTA | 59343 |
| rs112088141 | snp | C/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185624738 | CTGGGTCTGGTGGCA[C/T]GTGCTTATAATCCTA | 59343 |
| rs112424429 | snp | C/T | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185591907 | CCTAGCTGATTTTTG[C/T]ATTTTTTTTGTAGAA | 59343 |
| rs112452875 | snp | C/T | | | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631473 | TCCCCTCCCCCTCCC[C/T]CCCTCCCCCCTCCCT | 59343 |
| rs112563573 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185593843 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 59343 |
| rs112619161 | snp | A/G | 1.65233e-05 | 0.00287426 | intron-variant | SENP2 | GRCh38.p7 | 3:185624092 | CCACACGTGAGTGAC[A/G]ATCATCTACATGTGA | 59343 |
| rs112684125 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SENP2 | GRCh38.p7 | 3:185588628 | ATTGGTTGTTGGCTA[A/G]ATTGCATCGTGTGTT | 59343 |
| rs112800013 | snp | A/G | 0.380529 | 0.213219 | intron-variant | SENP2 | GRCh38.p7 | 3:185596019 | TGCCCAGACTGGAGT[A/G]CAGTGGTGCCATCTT | 59343 |
| rs112824329 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185629330 | ATAAATAATCTCAGC[A/C]CTTTGGGATGCTGAG | 59343 |
| rs112869755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185593130 | GAAGGATGGATAGGA[C/T]ATCAAAGGAGAGCAA | 59343 |
| rs113002547 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602830 | AGAGTGAGACTCTGT[C/G]TTAAAAAAAAAAAAA | 59343 |
| rs113334500 | snp | C/T | 1.71179e-05 | 0.00292552 | intron-variant | SENP2 | GRCh38.p7 | 3:185621945 | TACCCCCTGTTGAGG[C/T]GATCTCTCTTTTATC | 59343 |
| rs113403414 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185622810 | TTCATACTTTATTAC[A/T]TTCATGCTTTTTTTT | 59343 |
| rs113404329 | in-del | -/T | 0.272241 | 0.249009 | intron-variant | SENP2 | GRCh38.p7 | 3:185617375 | TATTTTTCTCAAGAG[-/T]CAGGTGTTGCCGAGA | 59343 |
| rs113473966 | snp | A/G | 0.272511 | 0.248984 | intron-variant | SENP2 | GRCh38.p7 | 3:185591044 | CGAGTAGCTGGGATT[A/G]CAGGCACCCACCACC | 59343 |
| rs113491716 | in-del | -/A | 0.130008 | 0.219321 | intron-variant | SENP2 | GRCh38.p7 | 3:185624865 | GAGCGAGACTGTCTC[-/A]AAAAAAAAAAAAAAG | 59343 |
| rs113537724 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185595536 | ATGTTTCTGGAAAGT[A/T]GTTTACATGTTCTGG | 59343 |
| rs113591110 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622537 | TAACAATAATATTGT[A/T]TTAGTATAAAATATT | 59343 |
| rs113645670 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185623662 | ACCCCATCTCTACTA[A/T]GAAAAATACAAAAAA | 59343 |
| rs113666252 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185605790 | AGATTTGTCACCAGC[A/C]GCTGTGACTGGGTGG | 59343 |
| rs113703842 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584719 | TGGCTAATTTTTGTA[-/T]TTTTTTTTTTTAGTA | 59343 |
| rs113997110 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185607289 | TAAGGAAGAAGAAAG[A/G]GTCATATTAGGAAGA | 59343 |
| rs114082515 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SENP2 | GRCh38.p7 | 3:185602646 | TTTGCAGCCTGGCCA[A/G]CATGGCGAGAAATCC | 59343 |
| rs114352754 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185626482 | ATTCAGCTCTCAATA[A/G]TAGTAGCTGGCCAGG | 59343 |
| rs114474252 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SENP2 | GRCh38.p7 | 3:185622978 | TCCGTCACTATGCCC[A/G]GCTAATTTTTGAATT | 59343 |
| rs114600627 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SENP2 | GRCh38.p7 | 3:185607926 | TTCAGAACACTCAGC[A/G]TGATGAAGAGTCAAT | 59343 |
| rs114654683 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SENP2 | GRCh38.p7 | 3:185591743 | TCTTTTCTATTTTTT[C/T]TTTTCGAGACAGGGT | 59343 |
| rs114689279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185586798 | TTAGGCTGAACACTA[A/G]CATTGAAGGAATACT | 59343 |
| rs114802568 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SENP2 | GRCh38.p7 | 3:185599313 | ATTTCCTGAGAACTT[A/T]CTCTGTGCCGGGTGC | 59343 |
| rs114818484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185618431 | ACTGCTTAGCCCCTG[C/T]ATGTTCTCTCTTTGA | 59343 |
| rs114888987 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185588600 | TAGTCTGAGAATGCA[C/G]GTTATTGATGAGATT | 59343 |
| rs114984018 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185626078 | AGACCTGTGGCTTCA[G/T]TTCTCACAAGGCCTG | 59343 |
| rs115016032 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SENP2 | GRCh38.p7 | 3:185629351 | GGATGCTGAGGCGGG[C/T]GGATCACCTGCAGTT | 59343 |
| rs115103058 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185596262 | AGCCACCGTGCCCAG[C/G]CTAAGATCTTCTAAC | 59343 |
| rs115158226 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185611883 | AGCATTGGGCCGGGC[A/G]CGGTGGCTTACGCCT | 59343 |
| rs115453472 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP2 | GRCh38.p7 | 3:185609805 | TCCTTCCCCCTGCCT[C/T]ACCCCTACCCCATGA | 59343 |
| rs115482339 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185621731 | AATTTATATTGGTAC[A/C]TGTATTTTTTAAAAG | 59343 |
| rs115525345 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SENP2 | GRCh38.p7 | 3:185593248 | AATGGCTGAAGACAG[A/G]TAGATCAAATTATCG | 59343 |
| rs115650735 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185588682 | ATTTTTCTCTCCTAT[C/T]TTTCCGTTGGGTTGA | 59343 |
| rs115764377 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585853 | TGACAATGCGTGAAA[A/T]GTACGAGGCAAAAGG | 59343 |
| rs115798619 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185606119 | TCTCTTTGTGTGGCA[A/G]CTCTAGTTTAGAAAC | 59343 |
| rs115799794 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185627300 | CCAAAGAAAGAGGTA[C/T]GTCAGTGTTTAATAG | 59343 |
| rs115865582 | snp | A/C | 0.347473 | 0.230215 | intron-variant | SENP2 | GRCh38.p7 | 3:185590810 | AGGTTGCAGTGAGCC[A/C]AGAATCTGCTACTGC | 59343 |
| rs115963311 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185593612 | TCACATCCTGTTTAT[G/T]TCACACAGAAAATCT | 59343 |
| rs116147655 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SENP2 | GRCh38.p7 | 3:185629315 | TGGTGGCTTTTGCCT[A/G]TAAATAATCTCAGCA | 59343 |
| rs116248151 | snp | C/T | 0.00225345 | 0.033491 | intron-variant | SENP2 | GRCh38.p7 | 3:185612565 | AACTATATTATTCAT[C/T]GATGAAGGAAACATT | 59343 |
| rs116462124 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185623412 | CCCAAAGTGTTGATA[C/T]ACAGGCGTGAGCCAC | 59343 |
| rs116646064 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185621736 | ATATTGGTACATGTA[G/T]TTTTTAAAAGATGCT | 59343 |
| rs116771692 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185625952 | ATTTCCTGTGGGGTC[A/G]GGTCATGCACTCCAT | 59343 |
| rs116789360 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185586660 | CTCCCGCCAGGCTGT[A/G]GGGAGGCAGCTCCTG | 59343 |
| rs116874060 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185611863 | AAAATACTGTCAAAT[A/C]TCACAGCATTGGGCC | 59343 |
| rs116973264 | snp | C/T | 0.0463947 | 0.145069 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630896 | TTGTGGAAGAAAATT[C/T]AGTACTTGGCTCTGA | 59343 |
| rs117267565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185589500 | ACCTGGGTTCATTTA[C/T]TAGCTAAGTGACTTT | 59343 |
| rs117894938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185614195 | TTACTATAAAGATAG[C/T]AGGGATTTATTCTGA | 59343 |
| rs137899961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185589109 | TGAATATAATTGATC[A/T]TAAGGGTTCAGAGAG | 59343 |
| rs137929876 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185622352 | CTATAATAGAAACCA[A/C]TCTTTAAAGCATACC | 59343 |
| rs138067080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185605815 | GGGTGGGAATTCCAG[C/G]CTTCAGTTCCTTTAG | 59343 |
| rs138129831 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185593497 | ATACCAATTTAGGAA[A/G]TGATTTTAGGGGATT | 59343 |
| rs138282304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185627217 | CTAGTCTTTGGTGAC[A/T]CAATGGGCACAATTT | 59343 |
| rs138381109 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SENP2 | GRCh38.p7 | 3:185592777 | GCCCACCACCACACC[C/T]GGCTAATTTTTGTAT | 59343 |
| rs138516803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185628467 | AGTAAGGGACATCCA[A/G]CTATTTATAATGATA | 59343 |
| rs138585673 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185599939 | GAGGAGCTGGGATTA[C/T]AGGCATGCGCCACCA | 59343 |
| rs138802256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185606830 | GAGGAGCAGAAAATC[A/G]TTGTGAAAGTATTGA | 59343 |
| rs138822131 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185610371 | TTCACCATGTTGGCC[A/G]GGCCGGTCTCGAACA | 59343 |
| rs138853881 | snp | A/G | 0.000148401 | 0.00861269 | missense | SENP2 | GRCh38.p7 | 3:185614640 | GCAGTGGAAGCAATG[A/G]CTTACTCAGGAGGAA | 59343 |
| rs139089688 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SENP2 | GRCh38.p7 | 3:185620233 | ATGCCTGGCTAATTT[A/T]TTTTAATTTATTTTA | 59343 |
| rs139158503 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SENP2 | GRCh38.p7 | 3:185628664 | GGAATGCGCCACCAC[C/T]CCTGGCTAATTTTGT | 59343 |
| rs139240725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185595424 | ATGAAAAACAACTCA[C/T]TTGCATAGTTTGGTA | 59343 |
| rs139257802 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SENP2 | GRCh38.p7 | 3:185616449 | GCATGCACTCCAGCC[C/T]GGGTGACAAAGTGAG | 59343 |
| rs139325415 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598535 | CACGGAATGTGGCCC[-/C]TTCAGGAGAGGTCAG | 59343 |
| rs139652446 | snp | A/T | 1.6601e-05 | 0.00288101 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185626303 | GTAATTTTAGGAGAT[A/T]CCTCAACAGCTGAAT | 59343 |
| rs139837525 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185629493 | TGAGGGACAAGAATC[A/G]CTCGAACCCAGGAGG | 59343 |
| rs139876720 | in-del | -/TT | 0.00676609 | 0.0577691 | intron-variant | SENP2 | GRCh38.p7 | 3:185627402 | CTTTCTGTTCTGCTC[-/TT]TTGTGTTTGTTTTGT | 59343 |
| rs139887115 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185624642 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 59343 |
| rs140100389 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SENP2 | GRCh38.p7 | 3:185601241 | GTAGATATGGGGTTT[C/T]GCTATGTTGGCCAGG | 59343 |
| rs140132991 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185596169 | CGGTTTCGCCATGAT[A/G]GTCAGGCTGGTCTTG | 59343 |
| rs140316187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185611872 | TCAAATCTCACAGCA[C/T]TGGGCCGGGCGCGGT | 59343 |
| rs140417864 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185618665 | GGGCGGATCACGAGG[G/T]CAGGAGACCGAGACC | 59343 |
| rs140520612 | snp | A/C | 0.0148355 | 0.084839 | intron-variant | SENP2 | GRCh38.p7 | 3:185614774 | ATCCTAAAAAGAGGC[A/C]TGTCTTTAAATAACC | 59343 |
| rs140551889 | snp | C/G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185588568 | GGGAGCTTGAGAGAA[C/G/T]AAGATGTCTAATACA | 59343 |
| rs140567825 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SENP2 | GRCh38.p7 | 3:185594815 | GTAGAGACGGAGTTT[C/T]ACCATATTGGCCAGG | 59343 |
| rs140684376 | snp | C/T | 0.272511 | 0.248984 | intron-variant | SENP2 | GRCh38.p7 | 3:185623821 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 59343 |
| rs140719881 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185592378 | CTTCAGTATATCTGA[A/G]TGGATAAAGAAAATA | 59343 |
| rs140735327 | snp | A/T | 0.486529 | 0.0809556 | intron-variant | SENP2 | GRCh38.p7 | 3:185590814 | TGCAGTGAGCCAAGA[A/T]TCTGCTACTGCACTC | 59343 |
| rs140862193 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185610657 | TCAAACTATTTTTGC[-/T]TTTTAAAGTTGCTGC | 59343 |
| rs140895855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185611268 | GGCGACAGTGCGAGA[C/G]TCCGTCTCAAAAAAC | 59343 |
| rs140936544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185625713 | CTATCCAGAACTTCT[C/G]TCTGTCCACCTTGAA | 59343 |
| rs140973730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185613691 | AAAAGTTAGCCAGGC[A/G]TGGTGGCATGTCTGT | 59343 |
| rs141049268 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630003 | CTGTACTCTAGTCCT[C/G]ACTTGGGGTGCAGAG | 59343 |
| rs141062273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185607775 | AAGCGATCCTCCAGC[A/G]TCAGCCTCCCAGAGT | 59343 |
| rs141145008 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185609927 | CAATTTTCCTTATAG[C/G]ACAGCTTGTTAATTA | 59343 |
| rs141200060 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185589696 | TCTTTTTAAAACAAG[A/G]TCTCACTCTTTTGAT | 59343 |
| rs141258915 | snp | A/G | 6.59207e-05 | 0.00574073 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598523 | CTTGTAATGGAACAC[A/G]GAATGTGGCCCCTTC | 59343 |
| rs141337295 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185594976 | TGATCCACCCACCTT[A/G]GCCTCCCAAAGTGCT | 59343 |
| rs141571597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185627920 | ATGAATACAAACTGT[A/G]ATACAAACTCTATTA | 59343 |
| rs141758117 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | SENP2 | GRCh38.p7 | 3:185620660 | CATGTTGGTCAGGCT[C/T]GTCTTGAACTCCTGA | 59343 |
| rs141841455 | snp | C/T | 6.60022e-05 | 0.00574428 | missense | SENP2 | GRCh38.p7 | 3:185624080 | CACAGCATGAAACCA[C/T]ACGTGAGTGACGATC | 59343 |
| rs141850932 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185628884 | TTTTTGTGTTGCTGC[-/T]TTGCAAATTGCCCAT | 59343 |
| rs141928522 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | SENP2 | GRCh38.p7 | 3:185610509 | ATTGTTTGCGAATAA[A/T]CAGTTGTGAACTTTA | 59343 |
| rs142010575 | snp | A/G | 0.000230939 | 0.0107432 | missense | SENP2 | GRCh38.p7 | 3:185614651 | AATGGCTTACTCAGG[A/G]GGAAAGTGTCAATAA | 59343 |
| rs142027475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622166 | AGATTTCTTTGGCAT[C/T]GATACGTTATTCTGA | 59343 |
| rs142112970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185603510 | GACTGAAGGAGATGA[A/C]AGATACCTGGTAACT | 59343 |
| rs142178004 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185598169 | AGGCGTGTGATACCA[C/T]CCGCAGCTAATTTTT | 59343 |
| rs142188043 | snp | C/T | 8.40258e-05 | 0.00648119 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598423 | CTAGATTGCTTTATT[C/T]ACCAAGTGAAAAACA | 59343 |
| rs142334232 | snp | C/G | 0.00795532 | 0.062565 | utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586309 | CACAAATCAGCGACC[C/G]AACTCTGGCGGTGGT | 59343 |
| rs142358798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185586849 | TTTACAAAGCACCCT[C/G]GCAAGTGTCATCTGC | 59343 |
| rs142400693 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185595669 | TTAGGACATAGGATA[-/T]TGTAGAAAGCTTACA | 59343 |
| rs142509319 | in-del | -/AATT | 0.00716266 | 0.059414 | intron-variant | SENP2 | GRCh38.p7 | 3:185627963 | AGGACTCCCGTGCTG[-/AATT]AATATAATTCCAGTA | 59343 |
| rs142572609 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185618167 | CAGGTTGGTCTCAAA[C/T]TCTGGACCTCAGGTG | 59343 |
| rs142657629 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185606622 | TTCCTACAATACAGC[C/T]TCCAACAAAATGAGG | 59343 |
| rs142899299 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | SENP2 | GRCh38.p7 | 3:185607310 | ATTAGGAAGAGATAA[G/T]ATTAGATTCTTTTTT | 59343 |
| rs143047729 | in-del | -/TTTA | 0.348574 | 0.229746 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584545 | CACACATGTATTTAT[-/TTTA]TTTATTTATTTTTTG | 59343 |
| rs143082277 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SENP2 | GRCh38.p7 | 3:185589418 | GATCATTTTCAAAAG[A/G]AAATTGCTTGTTTGT | 59343 |
| rs143300024 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP2 | GRCh38.p7 | 3:185619957 | CTGGTTGGTATCCAA[C/T]GCCTGGCCTCAAGTG | 59343 |
| rs143333225 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185618348 | ACTTGTCATCTTGTA[C/T]CCTTAATACATTTAG | 59343 |
| rs143348143 | snp | A/G | 5.06026e-05 | 0.00502978 | missense | SENP2 | GRCh38.p7 | 3:185611662 | TAAGTTCTCAAAGAA[A/G]TCAGATGGACACATT | 59343 |
| rs143573303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185609429 | GTATTGGTGGGAAGG[A/G]CTTTACTGAAAGAAG | 59343 |
| rs143677699 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SENP2 | GRCh38.p7 | 3:185614960 | TATTCAGCAAATGGG[G/T]AGTCGACACAGTCAT | 59343 |
| rs143680661 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185587534 | AATACTATACAAATT[C/G/T]TATGCCCCCTCTTCA | 59343 |
| rs143760415 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | SENP2 | GRCh38.p7 | 3:185596221 | TGCCCGCCTTTGCCT[C/G]CCAAAGTGCTGGGAT | 59343 |
| rs143767358 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SENP2 | GRCh38.p7 | 3:185589892 | CAGGCTGATGTCAAA[C/T]TCCAAGGCTCAAGCG | 59343 |
| rs143806982 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185597397 | TCACTCTGTCGCCCC[A/G]GCTGGAGTGGAGTGG | 59343 |
| rs143917972 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185588019 | GCTGGGATTACAGGC[C/T]TGAGCCACAGCGCCC | 59343 |
| rs144032990 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621667 | TGCTGGGATTACAGG[G/T]GTGAGCCACCATGCA | 59343 |
| rs144078841 | in-del | -/ATATATATATATATATATATAT | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584453 | ATTCTGGAATGCTAC[-/ATATATATATATATATATATAT]ATATATATATATATA | 59343 |
| rs144118984 | in-del | -/TTT | 0.486464 | 0.0811471 | intron-variant | SENP2 | GRCh38.p7 | 3:185593743 | TTGTGTTTTCATTTC[-/TTT]TTTTTTTTTTTTTTG | 59343 |
| rs144151983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628895 | CTGCTTTGCAAATTG[C/T]CCATGTAGTGATTCT | 59343 |
| rs144152215 | snp | G/T | 1.64846e-05 | 0.0028709 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586423 | CCTGGTATGTACAGA[G/T]GGCTGGTTAGGATTC | 59343 |
| rs144320001 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SENP2 | GRCh38.p7 | 3:185608874 | TGTTGGTGAGGCCAA[C/T]TCATTTTGGAAACTG | 59343 |
| rs144387716 | snp | C/G | 0.000148259 | 0.00860858 | missense | SENP2 | GRCh38.p7 | 3:185629792 | TGCAGCACCAGATGC[C/G]TCTCTTCCGGAAGAA | 59343 |
| rs144458538 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SENP2 | GRCh38.p7 | 3:185617936 | TAGTAGCTATTTTTT[G/T]GTTTTTGTTTTTTGG | 59343 |
| rs144496173 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185629307 | GCCGCCTGTGGTGGC[G/T]TTTGCCTATAAATAA | 59343 |
| rs144575077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185626121 | TATGATCTATGTTTT[A/G]TACCACATAGAGTAA | 59343 |
| rs144591804 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185600088 | AGGCGTGAGCCACTG[C/T]GCCCAGCCCAAAGAT | 59343 |
| rs144660871 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185613502 | AAGTATATATATATA[A/C]CTTTGATTGTTAATT | 59343 |
| rs144692437 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185624198 | TTTTAAAGTACACAT[-/T]CTTTTTTTTTCTTTC | 59343 |
| rs144714555 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185607256 | TTAGTCAATTTTTAG[A/G]TGTGGTTATTTTTAT | 59343 |
| rs144764471 | in-del | -/C | | | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631426 | TTGTACCACACCTCT[-/C]CCCCCCCCCTCCCAC | 59343 |
| rs144907474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185614192 | GAGTTACTATAAAGA[C/T]AGTAGGGATTTATTC | 59343 |
| rs144920748 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185608038 | CTGCTATTTCACTTG[C/T]CAACAGTTTTCTGAG | 59343 |
| rs145024660 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185613611 | CAAGGCAGAAGGATC[A/G]CTTGAGCCCAGGAGT | 59343 |
| rs145126254 | snp | C/T | 4.94654e-05 | 0.00497295 | missense | SENP2 | GRCh38.p7 | 3:185614618 | GTGTCGGCCCGACTC[C/T]GCCTGGGCAGTGGAA | 59343 |
| rs145156187 | snp | A/G | 0.000224093 | 0.0105828 | missense | SENP2 | GRCh38.p7 | 3:185606476 | GCAAGGGTCTGAGGC[A/G]TCCCCATTGTACTGT | 59343 |
| rs145169246 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SENP2 | GRCh38.p7 | 3:185591727 | TGGCTGAGGGAACCC[A/G]TCTTTTCTATTTTTT | 59343 |
| rs145212545 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185619566 | TTTTTTAAAAATAAT[G/T]CTGCCTTTTTCTGCC | 59343 |
| rs145392390 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185602379 | GGCATGCCACCCTGA[C/T]AGAGGAGGAGATTTC | 59343 |
| rs145474996 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SENP2 | GRCh38.p7 | 3:185629530 | TTGCAGTGAGCAGAT[C/T]GCGCCACTGCACTCC | 59343 |
| rs145496195 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185608992 | AGATGCCATCAGAAT[G/T]TAGCAGATAACATGA | 59343 |
| rs145533447 | in-del | -/ATAT | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584475 | ATATATATATATATA[-/ATAT]TATATATATATATAT | 59343 |
| rs145953958 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185627936 | ATACAAACTCTATTA[C/T]GTGAAGTAACTAGGA | 59343 |
| rs145966423 | in-del | -/TTATTA | 0.00757867 | 0.0610893 | intron-variant | SENP2 | GRCh38.p7 | 3:185628130 | GAGGACATCACTAGT[-/TTATTA]TTATTATTATTATTA | 59343 |
| rs146032713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185598267 | CACCTCAGCCTCCCA[A/T]AGTGTTGGGATTACA | 59343 |
| rs146095255 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SENP2 | GRCh38.p7 | 3:185601121 | CGATCTTGGCTCACT[A/G]TGACCTCTGCCTTCC | 59343 |
| rs146202454 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | SENP2 | GRCh38.p7 | 3:185628651 | AACCGTGATTACAGG[A/C]ATGCGCCACCACCCC | 59343 |
| rs146337020 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant | SENP2 | GRCh38.p7 | 3:185617555 | AGTGCTTTCAAATTG[C/G]GAATTACTCGAGGAG | 59343 |
| rs146445729 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185618174 | GTCTCAAACTCTGGA[C/G]CTCAGGTGATCCGCC | 59343 |
| rs146614483 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185591185 | GCTGGGGTTACAGGC[A/G]TGAGCCACCGCACCC | 59343 |
| rs146741908 | snp | A/G | 0.000547904 | 0.0165424 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185614716 | GAGGGACAGAAGAAC[A/G]GACGATCTCCTTGAA | 59343 |
| rs146844916 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185596826 | TAATCATGCCCTCAC[C/G]TCTGTGGTAAAAGTT | 59343 |
| rs146864951 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SENP2 | GRCh38.p7 | 3:185592218 | TGAGTAGCTGGGACT[A/G]TAGGCCCATACCACC | 59343 |
| rs146953476 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185593346 | AACTCCTGGGCTTAA[C/T]TAAGTGATCCTCTCA | 59343 |
| rs146963143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185597480 | GCATCAGCCTCCTGA[A/G]TAGCTGGGACTATAG | 59343 |
| rs147059005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185626902 | CCAACATGGAGAAAC[C/G]ATGTCTCTACTAAAA | 59343 |
| rs147069018 | in-del | -/AA | 0.0391387 | 0.134304 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185631095 | GGTCTGGCAGAACCT[-/AA]AAAAAAGTATATGCT | 59343 |
| rs147101040 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185620839 | GTACAGGTTTATTGC[A/G]GAAAAATGCATTTAT | 59343 |
| rs147219600 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185594290 | ATTCCCATTAAATAT[A/G]TAGTATGATTTTCTG | 59343 |
| rs147297104 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621705 | TAAATGGATTTCTAA[A/G]ATACATAAAAAATTT | 59343 |
| rs147397730 | snp | C/T | 3.29484e-05 | 0.00405871 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185629793 | GCAGCACCAGATGCC[C/T]CTCTTCCGGAAGAAG | 59343 |
| rs147526977 | snp | A/G | 0.000178548 | 0.00944682 | missense | SENP2 | GRCh38.p7 | 3:185611739 | ACTCAGTTTGTTCCA[A/G]AACAATGTGAGTTCC | 59343 |
| rs147536418 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185617809 | GTTTCCCTTTTCTGC[A/C/G]TCTGTATTTTATTGC | 59343 |
| rs147553782 | snp | A/C | 1.64811e-05 | 0.00287059 | missense | SENP2 | GRCh38.p7 | 3:185609299 | TATTGGAACGACTTA[A/C]AGAAAGTGGTCATGG | 59343 |
| rs147569516 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | SENP2 | GRCh38.p7 | 3:185608081 | TTTAGTTCATCAAAG[A/C]AATATTTATTGGGGT | 59343 |
| rs147570524 | in-del | -/G | | | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630604 | TGTGGTCACCTTAAA[-/G]AGACTTCCCCTTCTG | 59343 |
| rs147631072 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621393 | TTTTTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 59343 |
| rs147674987 | snp | A/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185586168 | GGGAGCGGTGCTAGG[A/T]TGCGCGTGCGCAGAT | 59343 |
| rs147793902 | snp | C/T | 0.000642753 | 0.0179154 | synonymous-codon, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598485 | CCCATTCCAGCTGAC[C/T]ACAAAGCCCATGGTA | 59343 |
| rs147873542 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SENP2 | GRCh38.p7 | 3:185626499 | AGTAGCTGGCCAGGC[A/G]TGGTGGCTCACACCT | 59343 |
| rs147886473 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185629486 | TGGAGACTGAGGGAC[A/G]AGAATCGCTCGAACC | 59343 |
| rs147959701 | in-del | -/CCCTCCCT | | | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631445 | CCCCCCTCCCACTCC[-/CCCTCCCT]CCCTCTCCCCTCCCC | 59343 |
| rs148075953 | snp | A/G | 3.30775e-05 | 0.00406665 | missense | SENP2 | GRCh38.p7 | 3:185619480 | TGGTGCCTATTCATC[A/G]GAAGGTACATTGGAG | 59343 |
| rs148086001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185615207 | AAGATGTGCCCACAT[C/T]TTGGCTTCCTCCACA | 59343 |
| rs148090383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600261 | CACTACTGTGTTTCT[C/G]TGAGTTTTGTGTAGT | 59343 |
| rs148210118 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SENP2 | GRCh38.p7 | 3:185589449 | TGTTTTTAAATCATT[G/T]CTGGAGCGAAAGAGA | 59343 |
| rs148255329 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604052 | CTTCAACCCGGAAGG[C/G]GGAGGTTGTAATGAG | 59343 |
| rs148366274 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185627561 | GGGACTACAGGCATG[C/T]GCCACCATGCCCAGC | 59343 |
| rs148399207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185618006 | CTGGAGTGCAATGGC[A/G]CAATCTTGGCTCAGC | 59343 |
| rs148499357 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185623001 | TTTGAATTTTTAGTA[A/G]AGACAGGGTTTCTCC | 59343 |
| rs148652006 | snp | A/G | 0.00039084 | 0.0139738 | synonymous-codon, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185590162 | ACCAGCCAAAAGACC[A/G]AGATTAGGTACTGAA | 59343 |
| rs148700910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185629184 | TAAGTAGAAAAGTTG[C/T]CTATTGTGCCACCAC | 59343 |
| rs148876807 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP2 | GRCh38.p7 | 3:185609174 | AAATAAAACACACCT[A/G]TGGTTTACATTTGGC | 59343 |
| rs148897420 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605677 | TTTTTTTTTTTTTTT[-/T]GAAACACCACATAAG | 59343 |
| rs149004097 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185587457 | ATTCTTATTTAGCAT[C/T]TACTCTTTGGAGTGT | 59343 |
| rs149097919 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185613532 | CTGTTGTTTTTCTTT[-/A]AAAAAAGCAGCAAGC | 59343 |
| rs149184727 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SENP2 | GRCh38.p7 | 3:185627471 | AGGCTGGAGTGCAGT[A/G]GCACGATCTCAGCTC | 59343 |
| rs149188369 | snp | C/T | 4.94752e-05 | 0.00497344 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185613384 | TACAGAGACGATGGT[C/T]GGAATCAGATTTGAA | 59343 |
| rs149268515 | in-del | -/TTT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592032 | TTTTTTTTTTTTTTT[-/TTT]GAGACAGGATCTTGC | 59343 |
| rs149279130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185592891 | CAAAGTGCTGGAATT[A/T]CAGGCGTGAGCCACC | 59343 |
| rs149445619 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SENP2 | GRCh38.p7 | 3:185622693 | ATTGTGCGCACATAC[A/C]TTTGCATTCATATGT | 59343 |
| rs149640328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185617913 | ACTGTATTTTAGGTG[A/C]ATTCTTATAGTAGCT | 59343 |
| rs149759411 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SENP2 | GRCh38.p7 | 3:185590858 | GGGCGACAGAGCGAC[A/G]CTCCATCTCAAAAAA | 59343 |
| rs149917990 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SENP2 | GRCh38.p7 | 3:185628747 | CTGGCCTCAGGTGAT[A/C]TGCCCACCTTGGCCT | 59343 |
| rs150017985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185595786 | TGGTGGCAAGGAAGG[A/G]TGAGCCTGAGATTTT | 59343 |
| rs150066095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185602193 | CTTTGAAGTTAGAGT[C/T]TTTATTCAAGTACTT | 59343 |
| rs150099233 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SENP2 | GRCh38.p7 | 3:185592627 | GGGTCTCCTTTTTTT[C/T]TTTTTTTGAGATGGA | 59343 |
| rs150214930 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SENP2 | GRCh38.p7 | 3:185615586 | TGACCTTAGATGATC[C/T]ACCCACCTCGGCCTC | 59343 |
| rs150430108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185610623 | ACGAACTCTTAACTT[C/T]GTCATGTTGGCGAAA | 59343 |
| rs150444786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185588571 | AGCTTGAGAGAACAA[G/T]ATGTCTAATACATTA | 59343 |
| rs150471029 | snp | C/T | 0.000695991 | 0.0186416 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185611711 | GGAAGAGCAAAATCA[C/T]GGAGTCAAAACAACT | 59343 |
| rs150528062 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621534 | AGCTAGGATTACAGG[C/G]GCGTGCCATCATGCC | 59343 |
| rs150684503 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185622287 | ATCTCAGAACCCAGG[A/G]GCAGTGTTTAAAGTG | 59343 |
| rs150784372 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SENP2 | GRCh38.p7 | 3:185589709 | AGGTCTCACTCTTTT[G/T]ATTAGGCTGGAGTGC | 59343 |
| rs150836620 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185595073 | AGAGATCTATGTAGT[C/T]TAGTTTCAGGGAAGT | 59343 |
| rs151002128 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP2 | GRCh38.p7 | 3:185625654 | AGTGTTTTTGCCTTA[C/T]GGCAGAACTGATCCA | 59343 |
| rs151050840 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185629730 | ACCTGAAGGTTGTGC[C/T]GCCATGCACATTAAT | 59343 |
| rs151141344 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185612869 | CCTTATCTCCCAGGC[G/T]TCAGGGGTTGGGAGA | 59343 |
| rs151152493 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SENP2 | GRCh38.p7 | 3:185597414 | CTGGAGTGGAGTGGC[A/G]TGATCTTGGCTCACT | 59343 |
| rs151246045 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185597036 | TTTTTGTATTTTTTT[-/T]AGAGACGGGATTTCA | 59343 |
| rs180762593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185627573 | ATGCGCCACCATGCC[A/C]AGCTAATTTTTGTAT | 59343 |
| rs180778364 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185603783 | GCACTGCTTAGGTGC[A/G]TTGTCCACATTTTGA | 59343 |
| rs180855922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185622681 | AGATGTGTATAAATT[A/G]TGCGCACATACATTT | 59343 |
| rs180890570 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630731 | TATAAACCTCAGAAT[A/T]GTAGGGGCTGGCCTG | 59343 |
| rs181008201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599568 | GAAATAGTTGTGATG[C/T]CTGCCACTCAGGAAG | 59343 |
| rs181028396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185586965 | ACCTGTTTTGTTCCA[A/G]AACAGCTGTCAAACA | 59343 |
| rs181051856 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | SENP2 | GRCh38.p7 | 3:185609702 | CTCCCTTCCCCACCC[C/G/T]ACTCCTGCCCCTCTC | 59343 |
| rs181104666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185598152 | CAGGTAGCTGGGACT[A/G]CAGGCGTGTGATACC | 59343 |
| rs181110051 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185588664 | GATACATGGTTTTGC[C/T]TTATTTTTCTCTCCT | 59343 |
| rs181345910 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185593325 | ATATTGCTCAGGCTG[A/C]TCTCGAACTCCTGGG | 59343 |
| rs181351274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185615492 | GGGATTACAGGCACC[C/T]GCCACCATGCCCAGC | 59343 |
| rs181449055 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185621610 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAT | 59343 |
| rs181741404 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185603451 | TACAAAACCATAGGC[C/T]TGTATTCATTAAAAA | 59343 |
| rs181757254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185594179 | TTAAAAAAAAAAAAC[A/G]CACACAAACGTTGGT | 59343 |
| rs181848229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185626710 | CCCAGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGG | 59343 |
| rs181911204 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185613827 | AATGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 59343 |
| rs181956432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599230 | ATTATCAGTGTCCTC[A/G]ATGTGACTTAGATCA | 59343 |
| rs181958966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185618027 | TTGGCTCAGCGCAAC[C/T]TCCACCTCCTGGGTT | 59343 |
| rs182138728 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185595312 | TTAAGCATCAATCGC[G/T]AAAGCTCTTCTTCTC | 59343 |
| rs182143576 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185618438 | AGCCCCTGCATGTTC[A/T]CTCTTTGAGGGAAGT | 59343 |
| rs182159992 | snp | A/C | 0.190205 | 0.242744 | intron-variant | SENP2 | GRCh38.p7 | 3:185616791 | AAAAAAAAAAAAAAA[A/C]GTTTAAAGTGGAAAT | 59343 |
| rs182354412 | snp | A/G | 0.000129518 | 0.00804626 | intron-variant | SENP2 | GRCh38.p7 | 3:185590172 | AGACCAAGATTAGGT[A/G]CTGAATATAAATTTT | 59343 |
| rs182420435 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185591107 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 59343 |
| rs182426320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185613489 | GAAAAGCAAGAAAAA[A/G]TATATATATATAACT | 59343 |
| rs182468213 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185624295 | GTGCTGGGATTACAG[G/T]TGTGAGCCACCATGC | 59343 |
| rs182523053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185607815 | ACAGGCGTGAGCCAC[C/T]GCGTCCAGTCATAAC | 59343 |
| rs182652867 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP2 | GRCh38.p7 | 3:185628655 | GTGATTACAGGAATG[C/T]GCCACCACCCCTGGC | 59343 |
| rs182921058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185623060 | AACCTCAGGTGATCC[A/G]CCCGCCCCAGCCTCC | 59343 |
| rs182975515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600502 | TTCATGGCCTCTTAA[C/T]AGTCCCATCAAGCAA | 59343 |
| rs183042991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185627957 | GTAACTAGGACTCCC[A/G]TGCTGAATTAATATA | 59343 |
| rs183052599 | snp | A/G | 0.00546017 | 0.0519641 | intron-variant | SENP2 | GRCh38.p7 | 3:185612603 | TTCTTTACCATCCTC[A/G]CAGATAGACTTGTTG | 59343 |
| rs183124901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599983 | TGTATTTTTAGTAGA[A/G]ACTGGGTTTCTCCGT | 59343 |
| rs183196447 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SENP2 | GRCh38.p7 | 3:185605227 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 59343 |
| rs183308076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628345 | TTTCACCATATTGGC[C/G]AGGCTGGTCTTGAAC | 59343 |
| rs183344710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185612272 | ATTATTCCTAAGCTG[C/T]TAGATAGTAGCAACT | 59343 |
| rs183432799 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185595665 | TTAATTAGGACATAG[G/T]ATATTGTAGAAAGCT | 59343 |
| rs183577421 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589429 | AAAGGAAATTGCTTG[C/T]TTGTTGTTTTTAAAT | 59343 |
| rs183690458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185619215 | TTAGTACCTTACCTT[C/T]GAATTCATCCTTATT | 59343 |
| rs183747779 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598014 | AAAATAGGACTTTTT[A/T]AAATTTTTGTTTTTC | 59343 |
| rs183755383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185621040 | TTGTGGGCATGGTGG[C/T]GCACACCTGTGAGAG | 59343 |
| rs183822401 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SENP2 | GRCh38.p7 | 3:185592587 | TGTGTTAGGTTTTAC[A/C]GAAAATACAAAAATT | 59343 |
| rs183924280 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185605561 | TCATGTCTCTTTGAT[C/T]TACTTTATTCTGCAA | 59343 |
| rs184183092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185625984 | TCATAGTTAGGGTTT[A/C]CAATCAAATGCAGAG | 59343 |
| rs184272902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185593394 | GTTGGGATTACAGGC[A/G]TGAACCACCATCCCC | 59343 |
| rs184280056 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SENP2 | GRCh38.p7 | 3:185616243 | TTTGGGAAGCCAAGA[C/T]GGGCGGATCATGAAG | 59343 |
| rs184309630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185603121 | TTCACTATGTTGGCC[A/G]GGCTGGTCTCGAACT | 59343 |
| rs184349526 | snp | A/G | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584397 | TAGCTTCAGGTGTGT[A/G]GCTGGTGATTCTGAA | 59343 |
| rs184359201 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185608546 | AAACCTCTCCTGGAA[C/G]CTCGTGGATATATGT | 59343 |
| rs184363733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185602252 | AGGAATGAGAAACTA[A/C]AAACTAGCGCCCTCT | 59343 |
| rs184478657 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185629235 | GAAGTTGTACTATAC[G/T]GTATAATTCTACATC | 59343 |
| rs184577048 | snp | C/T | | | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631437 | CTCTCCCCCCCCCCT[C/T]CCACTCCCCCTCCCT | 59343 |
| rs184633032 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621331 | AGACACATTTTTAAC[A/T]AAAAAAAAAAAAATA | 59343 |
| rs184786265 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185602758 | AGAATTGCTTGAACC[C/T]GGAAGCAGAGGGTGC | 59343 |
| rs184791873 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596729 | TGTTACCTGCCTGGG[A/G]AGTAAGGACAAGCTA | 59343 |
| rs184799473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185620288 | TGTTTTTTTGCCCAA[A/G]CTAGTCTTGAGCTCC | 59343 |
| rs184872506 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185625353 | CCTGACCTCGTGATC[C/T]GCCCGCCTCTGCCTC | 59343 |
| rs185069394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622877 | CACCCCATGCAGTGG[C/T]GCAGTCTCAGCTCAC | 59343 |
| rs185128119 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185613960 | TCTGCCTCCATACCA[A/G]CATGTTACCTACATT | 59343 |
| rs185145842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185594496 | AACTTTAAGTTAGGT[A/C]ACCATATCTGGCTAC | 59343 |
| rs185151788 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185628110 | TTTTAGCCCCCACCC[C/T]TAGGGAGGACATCAC | 59343 |
| rs185154357 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185618101 | AGGCATGCGCCACCA[C/T]GCCCGGCTAATTTTG | 59343 |
| rs185231183 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | SENP2 | GRCh38.p7 | 3:185592085 | AACAATTTTTTTTTT[A/T]AATTTTGTAAGAGGC | 59343 |
| rs185289212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185587522 | TCTGGAAAATAAAAT[A/G]CTATACAAATTCTAT | 59343 |
| rs185456644 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584996 | TGTGGGGCATGAAAA[C/T]CTTTGAGGATTCTTA | 59343 |
| rs185639674 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630579 | TATCCAAGCATCTTC[C/T]GAAGAGTGTTGTGGT | 59343 |
| rs185792420 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185608922 | AGCAGATGATTTCTG[C/T]TGAGTTTTTTTGTAG | 59343 |
| rs185887406 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185599598 | GGCTTGTAAAGTTGG[G/T]GGGGAAGGAAGTTAA | 59343 |
| rs185891773 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630844 | AAGTTTTCTACTCAT[G/T]AAGACTAACATCTCC | 59343 |
| rs185910535 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185605355 | CTGCCTGGAGGACAA[C/G]AGTGAAACTTCGTCG | 59343 |
| rs185940602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185610122 | TATATAATAGCAAAT[C/T]GAAGATTAAAAAGTC | 59343 |
| rs186009134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185603499 | AAATTGTTTCAGACT[A/G]AAGGAGATGAAAGAT | 59343 |
| rs186074037 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185627981 | TAATATAATTCCAGT[A/G]AAAAATAAAGGCATT | 59343 |
| rs186151196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185588768 | ATAAGGGTAGTATTT[A/G]TCTGTCCTACTCTGG | 59343 |
| rs186157546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185611537 | CTGTTGTAATTTGAT[A/G]TAATAGTGTAATCAA | 59343 |
| rs186214827 | snp | C/T | | | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631454 | CACTCCCCCTCCCTC[C/T]CTCTCCCCTCCCCCT | 59343 |
| rs186222042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185626973 | CCAGCTACTAGGGAG[G/T]CAGGCTGAGGCAGGA | 59343 |
| rs186339228 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185622292 | AGAACCCAGGGGCAG[A/T]GTTTAAAGTGTGTGG | 59343 |
| rs186387015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599232 | TATCAGTGTCCTCAA[G/T]GTGACTTAGATCAAG | 59343 |
| rs186401714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185627610 | CAGAGATGGGGTTTC[A/G]CCGTGTTGGCCAGGC | 59343 |
| rs186474303 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SENP2 | GRCh38.p7 | 3:185590552 | GGACTGTGTCAGGAA[A/G]AAAAAAAACAAAAAA | 59343 |
| rs186480309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185613285 | TTATTTCTAAAACTA[C/G]GATGTACTAGGTTTG | 59343 |
| rs186704443 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604469 | TTACAGGTGTTAGTG[A/C]TTTTTCTGTCAACTT | 59343 |
| rs186755253 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185617171 | GCTTTGTAGTTATAA[A/G]TTAAAATATTTTCAG | 59343 |
| rs186919205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185613757 | TGCTTGAGCCCAGGA[C/G]GTCAAGGCTGCAGTG | 59343 |
| rs186958806 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185594105 | TTATCTTTTTTTTTT[A/C]AGCCAAAAAAGGAAG | 59343 |
| rs187162288 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185618702 | ACTAACACGGTGAAA[C/G/T]CCCGTCTCTACTAAA | 59343 |
| rs187172555 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607888 | GAAGTAAATGGTGTG[C/T]ATCTCTGCTTTTTCC | 59343 |
| rs187353287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185589792 | TCCTGCCTTAGTGTA[C/G]CTGGGACCACACTCA | 59343 |
| rs187458639 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185591184 | TGCTGGGGTTACAGG[C/G]GTGAGCCACCGCACC | 59343 |
| rs187557276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185624602 | AAGTTTGGGCCAGGC[A/G]CGGTGGCTCACACTT | 59343 |
| rs187624640 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185612277 | TCCTAAGCTGCTAGA[C/T]AGTAGCAACTATTTT | 59343 |
| rs187675410 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185607522 | TTTAGTAGAGATGAG[A/T]TTTCACCACGTTGGC | 59343 |
| rs187718545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185602350 | CCAGAAAGTAAAGGA[A/G]TGTTCAAAAACTGGG | 59343 |
| rs187805722 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185597540 | TGTATTTTCAGTAGG[G/T]ACGGGGTTTCACTGT | 59343 |
| rs187813411 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185620555 | TCAAGCAATTCTCCT[A/G]CATCAGCCTCCTGAG | 59343 |
| rs187924683 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185623888 | AAAAAGCTAATGAAT[A/G]TGGATTTGAGAATGG | 59343 |
| rs187998254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185629083 | AGAAAGAAACTTGTA[G/T]ATTTTGTTGTTTTTT | 59343 |
| rs188050497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600674 | ATTTAGCTCTATGAT[A/G]TAGGTTGCTCACAGA | 59343 |
| rs188126593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185595362 | GAGTGTGTACTATCC[C/T]TCAGCACTATTAGAA | 59343 |
| rs188145193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185593176 | TTCTAGGCAGAGGGA[A/G]TAGTATGGGAAAGTT | 59343 |
| rs188155223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185615351 | TAGAAGAAAATAATT[C/T]CTTTTTTTTGAGACA | 59343 |
| rs188214278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185619795 | TGAACTGGTGTGATC[A/G]TAGCTCATTGCAGCC | 59343 |
| rs188456047 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185600247 | GCCTGAGATGCTGGC[A/G]CTACTGTGTTTCTGT | 59343 |
| rs188491333 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185595988 | TTATTTATTTTGAGA[A/T]GGAGTCTCACGCTGT | 59343 |
| rs188682802 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SENP2 | GRCh38.p7 | 3:185587695 | CCTCAGCCTCCCCAG[G/T]AGCTGGGACTACAGG | 59343 |
| rs188689024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185610952 | TACAGATCGAGACTC[C/T]GTCTCAAAATAAATA | 59343 |
| rs188769312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185623112 | GTGAGCCACCGTGCC[C/T]GGTGGTCTTTGGCTT | 59343 |
| rs188788776 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584833 | TGCTGGGATTACAGG[C/T]GTGTGCCACCACACC | 59343 |
| rs188796611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185608560 | AGCTCGTGGATATAT[G/T]TGATGGAAATTTTGA | 59343 |
| rs188853019 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185631065 | CTAGTGTTGCTTTTC[G/T]GATGTAATAAAAGGT | 59343 |
| rs188879019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185629453 | TGTGCTGGCACATAC[C/T]TGTAGTCCCAGCTAC | 59343 |
| rs188954070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185628429 | GGCATGTGCCACCAC[A/G]CCCGGTGACATCACT | 59343 |
| rs189084002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185627305 | GAAAGAGGTATGTCA[A/G]TGTTTAATAGCAAGG | 59343 |
| rs189242427 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SENP2 | GRCh38.p7 | 3:185614225 | AGTGATGGGATTGTG[A/G]GTCATATTTTTTGCT | 59343 |
| rs189325478 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185603385 | CATTCCTGCAAAAAC[A/G]ATAGACTCTAATCAT | 59343 |
| rs189339232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185603720 | GGAGATACACAGTTA[C/G]TCAGGGGTGAACTTA | 59343 |
| rs189491817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185602759 | GAATTGCTTGAACCC[A/G]GAAGCAGAGGGTGCA | 59343 |
| rs189512971 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185626577 | CAGGAGTTCAAGACC[A/C]GCCTGGCCAACATGG | 59343 |
| rs189514709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185616379 | AGGAGACTGAGGCAT[G/T]AAAATTGCTTGAACC | 59343 |
| rs189610212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185595195 | CCGAGATTTTGATAA[C/T]ATTCGTAGGAAAATA | 59343 |
| rs189694484 | snp | C/T | 0.0228947 | 0.104514 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185631093 | GGTGGTCTGGCAGAA[C/T]CTAAAAAAGTATATG | 59343 |
| rs189717002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185625357 | ACCTCGTGATCCGCC[C/T]GCCTCTGCCTCCCAA | 59343 |
| rs189781026 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598135 | CTCCCACCTCAGCCT[A/C]CCAGGTAGCTGGGAC | 59343 |
| rs189783486 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185593454 | ATACTAAATTCATTA[C/G]AACAGTATTTCCCAA | 59343 |
| rs189815314 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185618392 | TTAAGTTCTTTGACA[A/G]TTTTCTGGTGGGTTC | 59343 |
| rs189911433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185621578 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT | 59343 |
| rs190041319 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185621329 | TAAGACACATTTTTA[A/T]CTAAAAAAAAAAAAA | 59343 |
| rs190111080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599097 | TACATTTTGAAAATA[A/T]GAAAGGAAAACACTG | 59343 |
| rs190207047 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SENP2 | GRCh38.p7 | 3:185605208 | AACCCCATCTCTACT[C/T]AAAATACAAAAAATT | 59343 |
| rs190212246 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612516 | ATGTAGAGGAATGTC[G/T]TGATGTTGTGGAAAC | 59343 |
| rs190318621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185609111 | ATTTTTAAAAAATGT[A/G]TAAAGTTAGTAATTA | 59343 |
| rs190495305 | snp | A/C | | | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630647 | CTTGGCTTAGTCTTC[A/C]AACTGGATTCATGGA | 59343 |
| rs190529691 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185611596 | CAGAGATAATGCATA[C/T]TAATGGTAGACTTTG | 59343 |
| rs190559595 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585022 | TCTTAGGATTGTTTG[A/G]AAGAGGGGACTGGAT | 59343 |
| rs190562401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185592214 | CTCCTGAGTAGCTGG[A/G]ACTATAGGCCCATAC | 59343 |
| rs190740177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622339 | CAAATAGTAATTGCT[A/G]TAATAGAAACCAATC | 59343 |
| rs190741052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600450 | GAATAATTTACTCCA[A/G]TTGATTAGATTACAG | 59343 |
| rs190839925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185599288 | TAAAAAAAAACAAAA[A/G]AGCAAAAACATTTCC | 59343 |
| rs191074875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185605401 | AGGGCATTCACTTAC[A/T]TGATCATGGATTACC | 59343 |
| rs191166115 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SENP2 | GRCh38.p7 | 3:185618772 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 59343 |
| rs191186706 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SENP2 | GRCh38.p7 | 3:185628239 | CCTCTCAGGTTCAAG[C/T]GATTCTTCTGCCTCA | 59343 |
| rs191208272 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622578 | ATGGTTGTTTATCTT[G/T]AATAAAAAGCATAGA | 59343 |
| rs191212145 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185599601 | TTGTAAAGTTGGGGG[C/G]GAAGGAAGTTAAGGA | 59343 |
| rs191462767 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185589107 | TGTGAATATAATTGA[A/T]CATAAGGGTTCAGAG | 59343 |
| rs191559320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185597933 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 59343 |
| rs191567992 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP2 | GRCh38.p7 | 3:185620743 | CCACCGCACCTGGCC[A/G]AGGAGCTTTCATTTT | 59343 |
| rs191585844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622966 | GGAGTACAGGCTTCC[A/G]TCACTATGCCCGGCT | 59343 |
| rs191668179 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584258 | TGTAATGCCCCAAAC[G/T]TTCAGCAACAGCCTG | 59343 |
| rs191671579 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629131 | TTTCTCATAAAAAAA[A/C]AGAATATGTTCATTT | 59343 |
| rs191678357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185607954 | AATCTTTTTACTTTC[C/T]TTTTGAGGTTTTCTT | 59343 |
| rs191736525 | snp | A/G | 3.3089e-05 | 0.00406736 | intron-variant | SENP2 | GRCh38.p7 | 3:185613320 | ATCTAGCAGAAGTCT[A/G]TCATCTCTCAATTTT | 59343 |
| rs191943773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185612503 | CTGTAGCATTTCAAT[A/G]TAGAGGAATGTCTTG | 59343 |
| rs191976989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185594174 | TGTGGTTAAAAAAAA[A/C]AAACACACACAAACG | 59343 |
| rs192140593 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SENP2 | GRCh38.p7 | 3:185625740 | TGAAGCTGTAGGGTC[C/T]AAAGCAGTAGTCTTA | 59343 |
| rs192247361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185603098 | TGTATTTTTGGTAGA[A/G]ATGGGGTTTCACTAT | 59343 |
| rs192253303 | snp | A/C/G/T | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185589916 | TCAAGCGATCCTCCC[A/C/G/T]CTTGGCCTCCCAAAG | 59343 |
| rs192317729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185617668 | ATTTATTTATTATCT[A/G]TAATCAAAGTGACTC | 59343 |
| rs192391429 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SENP2 | GRCh38.p7 | 3:185628528 | TTTTTTTGTTTGAGA[C/T]GGAGTTTCGTTCTTG | 59343 |
| rs192467844 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598431 | ACTCACTTGGTGATA[C/T]TTCTGAAATGTGGTG | 59343 |
| rs192507740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185602226 | TACTCCTTGGCTATC[C/G]ACTTATATTTAGGAA | 59343 |
| rs192562675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185596006 | AGTCTCACGCTGTTG[C/T]CCAGACTGGAGTACA | 59343 |
| rs192619376 | snp | A/G | 6.59217e-05 | 0.00574078 | intron-variant | SENP2 | GRCh38.p7 | 3:185629740 | TGTGCTGCCATGCAC[A/G]TTAATATGTAATGCG | 59343 |
| rs192738150 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602716 | GCACACACCTGTAGT[C/T]CCTGCTACTTGGGAG | 59343 |
| rs192775402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185607605 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG | 59343 |
| rs192964716 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185591383 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAGGC | 59343 |
| rs192974222 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SENP2 | GRCh38.p7 | 3:185625078 | AGAAAAGTGTGAGGT[A/G]TATGCGTATGTATGG | 59343 |
| rs193007419 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185614275 | TCTTTTAAACATACT[A/T]ATTTTAATTGTGATA | 59343 |
| rs193119237 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185608724 | ATCTCCAGTGGAGAC[A/G]GAGAAAAAAGAATCA | 59343 |
| rs193187425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185613768 | AGGAGGTCAAGGCTG[C/T]AGTGAGCTGTGATCA | 59343 |
| rs193204417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185592308 | CTTGGAACTCCTGCC[C/T]TTCCAAAGTGCCGGG | 59343 |
| rs193269245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185619967 | TCCAACGCCTGGCCT[C/T]AAGTGGTTCTCCTGC | 59343 |
| rs193270664 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584834 | GCTGGGATTACAGGC[A/G]TGTGCCACCACACCC | 59343 |
| rs199540279 | in-del | -/A | 0.0520825 | 0.152737 | intron-variant | SENP2 | GRCh38.p7 | 3:185594557 | GGTTGCTTTTGAGAG[-/A]AAAAAAAAGCAAAGC | 59343 |
| rs199712543 | snp | A/G | 0.000355705 | 0.0133314 | intron-variant | SENP2 | GRCh38.p7 | 3:185606539 | TAAAAAAAATTTTAC[A/G]GCTCTTCCCAAGGAT | 59343 |
| rs199755812 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185608281 | TCTTAGATGAGAAAT[A/G]AGAAATGGGACTGAG | 59343 |
| rs199789737 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185594436 | CTCGAAATGTGGCTA[A/G]TTCAACTGAGGAACT | 59343 |
| rs199795987 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616870 | CCTGGGTTCAAATCT[C/T]CTTCTACCTTTTAAT | 59343 |
| rs199858955 | snp | A/G | 0.000148541 | 0.00861674 | missense | SENP2 | GRCh38.p7 | 3:185614663 | AGGAGGAAAGTGTCA[A/G]TAATTGAGACAAAGG | 59343 |
| rs200034691 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584506 | ATATATACACACATA[C/T]ACACACACACACACA | 59343 |
| rs200131839 | in-del | -/TA | 0.00146878 | 0.0270598 | intron-variant | SENP2 | GRCh38.p7 | 3:185590080 | ATGTGTGTGTAAATC[-/TA]TATATATATATTTTT | 59343 |
| rs200205604 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185611107 | ATGGCGAAACCCCAT[G/T]TCTACTAAAAATACA | 59343 |
| rs200250522 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185603938 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 59343 |
| rs200253544 | snp | A/G | 0.00011564 | 0.00760308 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185606366 | CTGTAATAGAAGACC[A/G]GGTGGCCGTCGCCAT | 59343 |
| rs200267000 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589075 | TCATTTTTTTTTTTT[-/T]GCATGTGTGAATATA | 59343 |
| rs200442929 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185601039 | ATATTTTCTTTTCTT[G/T]TCTTTTTTTTTTTTT | 59343 |
| rs200473769 | snp | C/T | 0.429837 | 0.173662 | intron-variant | SENP2 | GRCh38.p7 | 3:185621386 | GTTTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 59343 |
| rs200602306 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | SENP2 | GRCh38.p7 | 3:185629797 | CACCAGATGCCTCTC[C/T]TCCGGAAGAAGATGG | 59343 |
| rs200651806 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185620053 | TTCTTTTTCTTTTTC[-/T]TTTTTTTTTTTTAAA | 59343 |
| rs200720828 | snp | A/C/T | 3.4259e-05 | 0.00413867 | intron-variant | SENP2 | GRCh38.p7 | 3:185612662 | AAGTGAAAAGAGGTA[A/C/T]GTACATTCAGTTCAT | 59343 |
| rs200852457 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185612518 | GTAGAGGAATGTCTT[A/C/G]ATGTTGTGGAAACTC | 59343 |
| rs200868638 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607496 | ACCACGCCTGGCTAA[-/T]TTTTTGTATTTTTAG | 59343 |
| rs200990381 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185611366 | TCTTTTAATCTGAGT[A/C]TTATCACACTGAGAT | 59343 |
| rs201013825 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584498 | ATATATATATATATA[C/T]ACACATACACACACA | 59343 |
| rs201087781 | in-del | -/TGCT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622815 | ACTTTATTACATTCA[-/TGCT]TTTTTTTTTTTTTTT | 59343 |
| rs201130794 | snp | C/G | 0.000399973 | 0.014136 | missense | SENP2 | GRCh38.p7 | 3:185614726 | AGAACGGACGATCTC[C/G]TTGAACTTACAGAGG | 59343 |
| rs201200324 | in-del | -/GT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185587287 | CAGGTGTGCACCACC[-/GT]ACGCCTGGCTAATTT | 59343 |
| rs201270901 | snp | A/C | 9.8868e-05 | 0.00703024 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185600799 | AATAAGTGACTATCC[A/C]AAGATCAGAGTGACA | 59343 |
| rs201366840 | snp | C/T | 0.000510864 | 0.0159741 | intron-variant | SENP2 | GRCh38.p7 | 3:185629754 | CATTAATATGTAATG[C/T]GGGCGTTGTTTATGG | 59343 |
| rs201452746 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605371 | AGTGAAACTTCGTCG[-/A]AAAAAAAAAGAATAA | 59343 |
| rs201562693 | snp | A/C/G | 1.65111e-05 | 0.0028732 | synonymous-codon, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586473 | CTGCGACCGGTCGGT[A/C/G]CCCCCTGCCCGGGCC | 59343 |
| rs201595534 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | SENP2 | GRCh38.p7 | 3:185620434 | TTGTACTTGAGGAGC[-/T]TTTTTTTTGTTTGTT | 59343 |
| rs201876584 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607077 | ACCTCTGTCTCCCAC[A/G]TTCCAGCATATGTTA | 59343 |
| rs201975201 | snp | A/G | 5.25785e-05 | 0.00512704 | intron-variant | SENP2 | GRCh38.p7 | 3:185619265 | GATAATATGTTTGCC[A/G]TGTTCCAGCTTTTGC | 59343 |
| rs202119498 | in-del | -/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616791 | AAAAAAAAAAAAAAA[-/C]GTTTAAAGTGGAAAT | 59343 |
| rs202182503 | in-del | -/TTTA | 0.0376037 | 0.131863 | intron-variant | SENP2 | GRCh38.p7 | 3:185615860 | ATCTTATTTTGATGT[-/TTTA]TTTATTTATTTATTT | 59343 |
| rs202198191 | snp | C/T | 0.000314286 | 0.0125317 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185619319 | TAATTTTTACATGAA[C/T]CTTCTGGTGGAAAGA | 59343 |
| rs202228329 | in-del | -/CC | | | intron-variant | SENP2 | GRCh38.p7 | 3:185590947 | AGTCTTGCTCTGTCG[-/CC]CAGGCTGGAGTGCAG | 59343 |
| rs207464154 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605750 | GATGTCAGTTTGTTG[C/G]ATTGTTGGTAATGGC | 59343 |
| rs367699809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185629192 | AAAGTTGCCTATTGT[A/G]CCACCACGTGGATAT | 59343 |
| rs367821900 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185587110 | TAAAATTTGGGGGAA[-/A]CGCAAAGCTATTCTT | 59343 |
| rs367852027 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant | SENP2 | GRCh38.p7 | 3:185598973 | GTATTTTCGAACTCT[C/T]CATCTTGTGAACTGA | 59343 |
| rs367863848 | snp | A/G | 0.000307953 | 0.0124049 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185629859 | AGAAAACTTTGCCTG[A/G]TCCCTCTAGCTGCTG | 59343 |
| rs367866105 | snp | C/T | 5.02593e-05 | 0.00501269 | utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586384 | TTGCGTCTCGGGGTG[C/T]GTCGGCCGCCGCTGC | 59343 |
| rs368061960 | snp | C/G | 6.94541e-05 | 0.00589256 | intron-variant | SENP2 | GRCh38.p7 | 3:185619536 | TGGTTAATTGTTGGA[C/G]TTGGATAAAGGCCAT | 59343 |
| rs368207503 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185620473 | TTTGAGATGGAGTCT[C/T]GCTCTGTTTCCCAGG | 59343 |
| rs368247223 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SENP2 | GRCh38.p7 | 3:185629765 | AATGCGGGCGTTGTT[C/T]ATGGGGTTCTTTGCA | 59343 |
| rs368260858 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584452 | AATTCTGGAATGCTA[C/T]ATATATATATATATA | 59343 |
| rs368332244 | snp | A/G/T | 6.5945e-05 | 0.00574184 | missense | SENP2 | GRCh38.p7 | 3:185609278 | AAAGAGAGAAGTACC[A/G/T]AAAGTTATTGGAACG | 59343 |
| rs368419427 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | SENP2 | GRCh38.p7 | 3:185614762 | TTCTTTGTATTGATC[C/T]TAAAAAGAGGCATGT | 59343 |
| rs368457415 | in-del | -/TC | | | intron-variant | SENP2 | GRCh38.p7 | 3:185601040 | TATTTTCTTTTCTTG[-/TC]TTTTTTTTTTTTTTT | 59343 |
| rs368497606 | snp | A/C | 1.65474e-05 | 0.00287636 | intron-variant | SENP2 | GRCh38.p7 | 3:185617631 | GTTGTATTCCCTCCC[A/C]CTTTTGGCTATCATT | 59343 |
| rs368536548 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP2 | GRCh38.p7 | 3:185591635 | GGATTACAGGCGTGA[A/G]CCCCCGCGCCTGGCC | 59343 |
| rs368562844 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604275 | TTCTAGTTTAATTCT[A/G]TTATGGTTAGAGAAT | 59343 |
| rs368591303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185625256 | AGCTGGGACCACAGG[C/T]GCCTGCCACCACGCC | 59343 |
| rs368609468 | snp | C/T | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584343 | GATTTGCTTCCATCC[C/T]CTAGGATATGACCCC | 59343 |
| rs368635058 | snp | C/T | 2.05662e-05 | 0.00320666 | intron-variant | SENP2 | GRCh38.p7 | 3:185606504 | TGTGGAGGAGGTAAG[C/T]CTTTTCAGCTTGATT | 59343 |
| rs368675500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185598203 | ACAAATGGGGTTTCT[C/T]CATGGTGGCCCAAGC | 59343 |
| rs368792796 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185628931 | AAAGCAGAATCATTT[A/G]TTAAGCAAAACATCT | 59343 |
| rs368980670 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185599588 | CACTCAGGAAGGCTT[A/G]TAAAGTTGGGGGGGA | 59343 |
| rs368988878 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592350 | GAGCCACTGTGCCCA[A/G]CCAAGTCTTTTACTT | 59343 |
| rs369052913 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SENP2 | GRCh38.p7 | 3:185611748 | GTTCCAAAACAATGT[A/G]AGTTCCCAGATTTAG | 59343 |
| rs369071463 | snp | C/G/T | 3.32089e-05 | 0.00407475 | missense | SENP2 | GRCh38.p7 | 3:185621836 | TATAGGTGATTGACC[C/G/T]AAGAAAAAAGTGTCT | 59343 |
| rs369165720 | in-del | -/AC | 0.488545 | 0.074807 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584505 | TATATATACACACAT[-/AC]ACACACACACACACA | 59343 |
| rs369274976 | snp | C/T | 6.62164e-05 | 0.00575359 | intron-variant | SENP2 | GRCh38.p7 | 3:185624105 | ACGATCATCTACATG[C/T]GACATACTTGGTTGC | 59343 |
| rs369299273 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185626841 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 59343 |
| rs369443283 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185623188 | CTCTTGCTGCCCAGG[C/G]TGGAGTGCAATGGCG | 59343 |
| rs369451498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600407 | TTTTAGGTATGTTAC[C/T]GGCCAAACATACGGC | 59343 |
| rs369464436 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592441 | TGCTATAATAATATA[C/T]TCCTCTTTCTCAAAA | 59343 |
| rs369642239 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185591756 | TTTTTTTCGAGACAG[G/T]GTCTCATTCTGTCAC | 59343 |
| rs369656967 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185606963 | CAAATAATATATCTA[C/T]TATGTTATATATTTC | 59343 |
| rs369766822 | snp | C/G | 9.90737e-05 | 0.00703754 | intron-variant | SENP2 | GRCh38.p7 | 3:185613340 | CTCTCAATTTTTTTC[C/G]TTAGGTGTTCAAAGG | 59343 |
| rs369774061 | snp | C/T | 0.000828717 | 0.0203389 | intron-variant | SENP2 | GRCh38.p7 | 3:185621932 | TTGAAAACCTCACTA[C/T]CCCCTGTTGAGGTGA | 59343 |
| rs369840467 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616644 | GCCGGGCGTGGTGGC[A/G]GGCGCCTGTCATCCC | 59343 |
| rs369863150 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629762 | GTAATGCGGGCGTTG[-/T]TTTATGGGGTTCTTT | 59343 |
| rs369874440 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185627676 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 59343 |
| rs369883507 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185588444 | GATCCACCCGCCTCG[A/G]CCTCCCAAAATGCTG | 59343 |
| rs369951626 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185617844 | ACCACTTCATTTACT[A/G]GTCTTCAATAAACCC | 59343 |
| rs369984729 | snp | A/G | 1.65529e-05 | 0.00287683 | intron-variant | SENP2 | GRCh38.p7 | 3:185613314 | TGAATCATCTAGCAG[A/G]AGTCTATCATCTCTC | 59343 |
| rs369989369 | in-del | -/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185601041 | ATTTTCTTTTCTTGT[-/C]TTTTTTTTTTTTTTT | 59343 |
| rs370115111 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | SENP2 | GRCh38.p7 | 3:185599016 | CCTGGAACAACATGC[C/T]GAAACTGGGTGAGGT | 59343 |
| rs370190294 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598127 | AGGTGATCCTCCCAC[C/T]TCAGCCTCCCAGGTA | 59343 |
| rs370242775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185589226 | CATAATGTAGTTTGC[A/G]TGATAAAAATGAAGT | 59343 |
| rs370299367 | snp | C/G | 0.000497099 | 0.0157576 | intron-variant | SENP2 | GRCh38.p7 | 3:185614535 | AAGTATCAAACATGT[C/G]AGTAGAATTTAGATA | 59343 |
| rs370379342 | snp | G/T | 0.000560298 | 0.0167283 | intron-variant | SENP2 | GRCh38.p7 | 3:185629748 | CATGCACATTAATAT[G/T]TAATGCGGGCGTTGT | 59343 |
| rs370386642 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185594683 | GGAGTGCAGTGGCAC[A/G]ATCTCGGTTCACTGC | 59343 |
| rs370388997 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185623763 | ACCCGGGAGGCAGAG[A/C/G]TTGCAGTGAGCCGAG | 59343 |
| rs370445840 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185593564 | TTATGTACTAAGAAA[G/T]GTGTATCCTTTTCAG | 59343 |
| rs370450780 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612669 | AAGAGGTACGTACAT[C/T]CAGTTCATTCTACAC | 59343 |
| rs370547214 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185627277 | TTCCTGTGTATTATT[A/T]TTTCTAGCCAAAGAA | 59343 |
| rs370601182 | snp | G/T | 5.07292e-05 | 0.00503607 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598419 | CTTTCTAGATTGCTT[G/T]ATTCACCAAGTGAAA | 59343 |
| rs370700553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185613156 | GATGTGCCCAAGACC[A/C]TAAAACCTGCAAAGC | 59343 |
| rs370741390 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SENP2 | GRCh38.p7 | 3:185629771 | GGCGTTGTTTATGGG[A/G]TTCTTTGCAGCACCA | 59343 |
| rs370822793 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185608463 | TTACAAAGATAACCC[C/T]ATGTTTATGGGGAAG | 59343 |
| rs370964129 | snp | A/G | 0 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185594088 | ACAGTAGTAATTTAA[A/G]ATTATCTTTTTTTTT | 59343 |
| rs371186048 | snp | C/T | 8.4827e-05 | 0.00651201 | intron-variant | SENP2 | GRCh38.p7 | 3:185614756 | GTATTGTTCTTTGTA[C/T]TGATCCTAAAAAGAG | 59343 |
| rs371224201 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598039 | TTTTTCAGAGACAGA[G/T]TCTCACTCTGTTGCC | 59343 |
| rs371334519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185605097 | CATTCAAGACTGGGC[A/G]TGGTGGCTCACGCCT | 59343 |
| rs371529581 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185610740 | AGGTGGACGGATCAC[A/G]AGGTCAGGAGATCAA | 59343 |
| rs371531414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185610457 | GTGAGCCACCGCACC[C/T]GGCCTACTATCTAGC | 59343 |
| rs371539949 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185590747 | ACGCCTATAGTCACA[C/G]CTACTCGGGAGGCTG | 59343 |
| rs371706218 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | SENP2 | GRCh38.p7 | 3:185599597 | AGGCTTGTAAAGTTG[C/G]GGGGGAAGGAAGTTA | 59343 |
| rs371741618 | snp | C/T | 5.02138e-05 | 0.00501043 | intron-variant | SENP2 | GRCh38.p7 | 3:185598588 | ATACTGATCTTTATA[C/T]TTAATCATTATATTT | 59343 |
| rs371780448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185615393 | TTGTTGCCCAGGCTG[A/G]AGTGCAATGGCGCGA | 59343 |
| rs371821065 | in-del | -/ATG | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612519 | TAGAGGAATGTCTTG[-/ATG]TTGTGGAAACTCTGT | 59343 |
| rs371823702 | snp | C/T | 1.65124e-05 | 0.00287331 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185629893 | GTTCTTTCACAGACA[C/T]TTCCATATACCTCAT | 59343 |
| rs371843790 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629394 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 59343 |
| rs371906302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185615534 | TTTTTAGTAGAGACC[A/G]GGTTTCACCATGTTG | 59343 |
| rs371913752 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185625359 | CTCGTGATCCGCCCG[C/T]CTCTGCCTCCCAAAG | 59343 |
| rs371941217 | snp | C/T | 1.7413e-05 | 0.00295062 | intron-variant | SENP2 | GRCh38.p7 | 3:185619538 | GTTAATTGTTGGACT[C/T]GGATAAAGGCCATTT | 59343 |
| rs371947025 | snp | A/G/T | 1.77247e-05 | 0.00297692 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185590127 | AGCACTCTGTTTTCT[A/G/T]CAGTGGACACTGATG | 59343 |
| rs372079903 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598347 | GAGGCTCTTTCCAAG[A/G]TATCATTTTATTTTT | 59343 |
| rs372085045 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185609473 | GAGAACTAGCTCTGT[C/T]ATTTGCCTGGATATT | 59343 |
| rs372368329 | snp | A/G | 0.000155126 | 0.00880561 | intron-variant | SENP2 | GRCh38.p7 | 3:185614524 | TTTATATTTGCAAGT[A/G]TCAAACATGTCAGTA | 59343 |
| rs372438580 | snp | C/T | 1.65343e-05 | 0.00287521 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185621859 | AAGTGTCTTAAATAT[C/T]TGGATTCTATGGGAC | 59343 |
| rs372470917 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185595014 | CAGGTGTGAGCCACC[A/G]TACCTGGCTCAGGCT | 59343 |
| rs372530782 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185611042 | GCGCTTTGGGAGGCC[A/G]AGGCAGGTGGGTCAC | 59343 |
| rs372673843 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596436 | ACCAGCCTGGGCAAC[A/G]TAGTGAGACCTGCCT | 59343 |
| rs372679727 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616745 | GCGCCACTGCACTCC[C/G]GCCTGGGAGACTGAG | 59343 |
| rs372683160 | snp | G/T | 1.69395e-05 | 0.00291024 | intron-variant | SENP2 | GRCh38.p7 | 3:185609211 | ATTATAAATTTAATG[G/T]GCTGGTACTTATCTA | 59343 |
| rs372704421 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185612802 | AGGGTAGATAGGTAG[A/C]TAGCTGTTGTGTCAG | 59343 |
| rs372713428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185607817 | AGGCGTGAGCCACCG[C/T]GTCCAGTCATAACTT | 59343 |
| rs372778239 | snp | A/T | 1.66291e-05 | 0.00288345 | intron-variant | SENP2 | GRCh38.p7 | 3:185624125 | TACTTGGTTGCATTT[A/T]CTAATAGTATATTAT | 59343 |
| rs372892265 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185617790 | TCTGCCTTTGATTAG[C/T]GATGTTTCCCTTTTC | 59343 |
| rs372945373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185627229 | GACACAATGGGCACA[A/G]TTTGCAAATCTCTGA | 59343 |
| rs372977692 | snp | A/T | 4.95258e-05 | 0.00497599 | intron-variant | SENP2 | GRCh38.p7 | 3:185613342 | CTCAATTTTTTTCCT[A/T]AGGTGTTCAAAGGGG | 59343 |
| rs372990775 | snp | A/G/T | 0.000128745 | 0.00802231 | intron-variant | SENP2 | GRCh38.p7 | 3:185606295 | AATTTAAGCAGCTTG[A/G/T]TGATACTTTTTTTCT | 59343 |
| rs373113187 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630355 | AACTCTCACTGGGGG[C/T]GGAAGGAAGTGGAGC | 59343 |
| rs373176516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185612122 | AGATCACGCCACTGC[A/G]CTCCAGCCTGGGTGA | 59343 |
| rs373183850 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185588520 | TTAAATTAAGCCTCA[A/C]TATCAAGAAAAGTGG | 59343 |
| rs373433804 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185591942 | GGTCTTGCCACATTG[C/T]CCAGGCTGAAAATAG | 59343 |
| rs373475345 | snp | A/G | | | downstream-variant-500B | SENP2 | GRCh38.p7 | 3:185631209 | GTGCACGTGTTACCT[A/G]TGAATCTACACGCCT | 59343 |
| rs373486029 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622106 | ACAAGTTTGTCATGT[A/T]TTATGATGTAAAATA | 59343 |
| rs373584946 | snp | C/T | 0.000115374 | 0.0075943 | intron-variant | SENP2 | GRCh38.p7 | 3:185629752 | CACATTAATATGTAA[C/T]GCGGGCGTTGTTTAT | 59343 |
| rs373607546 | snp | C/T | 0.000115499 | 0.00759844 | intron-variant | SENP2 | GRCh38.p7 | 3:185599054 | AATATTTCTGTTTCC[C/T]GCTACCTCCTTCTGC | 59343 |
| rs373638583 | snp | C/G | 1.70055e-05 | 0.0029159 | intron-variant | SENP2 | GRCh38.p7 | 3:185621938 | ACCTCACTACCCCCT[C/G]TTGAGGTGATCTCTC | 59343 |
| rs373864508 | snp | C/G | 8.27342e-05 | 0.00643119 | intron-variant | SENP2 | GRCh38.p7 | 3:185613318 | TCATCTAGCAGAAGT[C/G]TATCATCTCTCAATT | 59343 |
| rs373940933 | snp | A/G | 0.000168458 | 0.00917609 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185611666 | TTCTCAAAGAAGTCA[A/G]ATGGACACATTAAAG | 59343 |
| rs374000966 | snp | A/G | | | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185631096 | GGTCTGGCAGAACCT[A/G]AAAAAGTATATGCTG | 59343 |
| rs374034563 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598226 | GCCCAAGCTGGTCTC[A/G]AGCTCCTGGGCTCAA | 59343 |
| rs374048921 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185608097 | AATATTTATTGGGGT[C/T]CCAGGTACTGTGCTA | 59343 |
| rs374074132 | snp | A/G | 1.64863e-05 | 0.00287104 | missense | SENP2 | GRCh38.p7 | 3:185624036 | AGACCAAAAGAAATA[A/G]TGATCTGAATCTTTT | 59343 |
| rs374080521 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP2 | GRCh38.p7 | 3:185626650 | TGGTGGTGCATGCCT[A/G]TAATCCCAGCTACTC | 59343 |
| rs374225020 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185589907 | CTCCAAGGCTCAAGC[A/G]ATCCTCCCCCTTGGC | 59343 |
| rs374269045 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602562 | TAGAAAATCACCATT[C/T]TGTAACTGTCATGGT | 59343 |
| rs374448379 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185610503 | TAACAGATTGTTTGC[A/G]AATAATCAGTTGTGA | 59343 |
| rs374523198 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185623381 | CCGACCTCAGGTGAT[C/T]CATCCGCCTTGGCCT | 59343 |
| rs374574329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185604059 | CCGGAAGGCGGAGGT[C/T]GTAATGAGCTGAGAT | 59343 |
| rs374595095 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185625134 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 59343 |
| rs374637352 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185598456 | CTCTACAATGCTGCC[A/G]GCTTATTTGGATTCC | 59343 |
| rs374726679 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185596448 | AACATAGTGAGACCT[G/T]CCTCTACCAAAAAAT | 59343 |
| rs374754196 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616762 | CCTGGGAGACTGAGC[A/G]AGACTCCGTCTCCAA | 59343 |
| rs374819138 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SENP2 | GRCh38.p7 | 3:185614069 | TTCTATTTGTTTACT[A/G]CAATTGTGGTTATAT | 59343 |
| rs375162066 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185598585 | GGAATACTGATCTTT[A/G]TACTTAATCATTATA | 59343 |
| rs375199243 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SENP2 | GRCh38.p7 | 3:185623805 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 59343 |
| rs375321755 | snp | G/T | 1.70758e-05 | 0.00292192 | intron-variant | SENP2 | GRCh38.p7 | 3:185617438 | TAACTGATAATGAAT[G/T]GTTCTATATTAAAAT | 59343 |
| rs375370519 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185599722 | GTTTTAAAAAGTACC[A/T]CTAGGAGTAGAGAAG | 59343 |
| rs375374349 | snp | C/G | 1.74579e-05 | 0.00295443 | intron-variant | SENP2 | GRCh38.p7 | 3:185612670 | AGAGGTACGTACATT[C/G]AGTTCATTCTACACT | 59343 |
| rs375412509 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | SENP2 | GRCh38.p7 | 3:185590328 | CAAGGCAGGCGGATC[A/C]CCTGAGGTCAGGAGT | 59343 |
| rs375476062 | snp | C/T | 3.30699e-05 | 0.00406618 | missense | SENP2 | GRCh38.p7 | 3:185619479 | CTGGTGCCTATTCAT[C/T]GGAAGGTACATTGGA | 59343 |
| rs375526849 | in-del | -/TACATATATATATATATATATATATATATA | | | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584450 | ACAATTCTGGAATGC[lengthTooLong]TATATATATATATAT | 59343 |
| rs375611927 | snp | G/T | 3.30595e-05 | 0.00406554 | missense | SENP2 | GRCh38.p7 | 3:185614683 | TGAGACAAAGGAAAA[G/T]AATTGCTCAGGCAAA | 59343 |
| rs375718504 | snp | A/G | 0.000395446 | 0.0140558 | intron-variant | SENP2 | GRCh38.p7 | 3:185629759 | ATATGTAATGCGGGC[A/G]TTGTTTATGGGGTTC | 59343 |
| rs375754849 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185611882 | CAGCATTGGGCCGGG[C/T]GCGGTGGCTTACGCC | 59343 |
| rs375819185 | snp | A/T | 3.29636e-05 | 0.00405964 | intron-variant | SENP2 | GRCh38.p7 | 3:185629742 | TGCTGCCATGCACAT[A/T]AATATGTAATGCGGG | 59343 |
| rs375851777 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604997 | CTGACCTCGTGATCC[A/C]CCCGCCTCAGCCTCC | 59343 |
| rs375987673 | snp | C/G/T | 6.63244e-05 | 0.00575833 | intron-variant | SENP2 | GRCh38.p7 | 3:185613450 | ATACCTGTTTACTTA[C/G/T]GTAACTTATGTTTTG | 59343 |
| rs376042555 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584320 | GAGGCGGGTGTGTCC[A/G]CACTTAGGATTTGCT | 59343 |
| rs376119566 | in-del | -/GT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185597214 | TTCAGAACATTTTGA[-/GT]GTGTGTGTGTGTGTG | 59343 |
| rs376152151 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | SENP2 | GRCh38.p7 | 3:185624025 | GGATGAAAGTAAGAC[C/G]AAAAGAAATAGTGAT | 59343 |
| rs376159083 | in-del | -/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185617950 | TTGTTTTTGTTTTTT[-/G]GTTTTGTTTTTGAGA | 59343 |
| rs376199027 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185588676 | TGCCTTATTTTTCTC[G/T]CCTATCTTTCCGTTG | 59343 |
| rs376210485 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185628571 | GAGTGCAATGGCGCA[A/G]TCTCAGCTCACTGCA | 59343 |
| rs376221825 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629694 | AAAGCACATGGACAT[C/T]CTGCTTTATTACATG | 59343 |
| rs376248659 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185622533 | TTGCTAACAATAATA[A/T]TGTTTTAGTATAAAA | 59343 |
| rs376418606 | snp | C/T | 3.36842e-05 | 0.00410378 | intron-variant | SENP2 | GRCh38.p7 | 3:185606543 | AAAAATTTTACAGCT[C/T]TTCCCAAGGATGCTG | 59343 |
| rs376597539 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607999 | TTTAGAATTATTCCT[A/G]TACCTGGCACTCCCG | 59343 |
| rs376702743 | snp | C/G | 6.68237e-05 | 0.00577991 | intron-variant | SENP2 | GRCh38.p7 | 3:185621915 | TCTCCTGTAAGTAAA[C/G]GTTGAAAACCTCACT | 59343 |
| rs376726268 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585763 | AATAACTTAATCGCT[C/T]TATGCCTCAATTTCC | 59343 |
| rs376754622 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605484 | ATTTAAATTTTTCTC[A/T]TATAGCTTTTTCTTT | 59343 |
| rs376766311 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185593873 | AGCTGGGATTACAGG[C/T]GCCCACCACTATGCC | 59343 |
| rs376792154 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185615822 | TCATGTCAAAAAGGA[G/T]GGTGTGACCCCTTAG | 59343 |
| rs376822227 | snp | A/G | 5.34126e-05 | 0.00516754 | missense | SENP2 | GRCh38.p7 | 3:185611719 | AAAATCACGGAGTCA[A/G]AACAACTCAGTTTGT | 59343 |
| rs376889216 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185586012 | TGGAGCAGCCTCACA[C/T]GTGGCCTGTGGGCCT | 59343 |
| rs376906179 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629707 | ATCCTGCTTTATTAC[A/G]TGATTACACCTGAAG | 59343 |
| rs376997865 | in-del | -/TT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185594621 | TTCAGGCTCATGATC[-/TT]TTTTTTTTTTTTTTT | 59343 |
| rs377025225 | snp | A/T | 0.000212736 | 0.0103113 | intron-variant | SENP2 | GRCh38.p7 | 3:185611624 | TTGCTTTTGTATCTG[A/T]TCTCCCTCACTTTTT | 59343 |
| rs377073134 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185611292 | AAAAAACAAAAAGTT[A/C]TTGCTTTTAATGTAT | 59343 |
| rs377237755 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185624335 | GTCTACATCTTAAGA[A/C]TGATCTGCTTCTAAA | 59343 |
| rs377283543 | snp | C/G | 1.64822e-05 | 0.00287068 | missense, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586438 | TGGCTGGTTAGGATT[C/G]TCGGCACCATTTTCC | 59343 |
| rs377411258 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185619798 | ACTGGTGTGATCATA[A/G]CTCATTGCAGCCTGG | 59343 |
| rs377419389 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621230 | CAGATATAAAGAAAG[A/C]AAAAAAAAAAAAAAA | 59343 |
| rs377754719 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185607389 | GCTAGAGTGCAATGG[C/T]GCGATCTTGGCTCAC | 59343 |
| rs386398774 | in-del | -/TTT | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592012 | AACCGGTAATATTTC[-/TTT]TTTTTTTTTTTTTTT | 59343 |
| rs386398775 | in-del | -/TT | 0.499942 | 0.00539106 | intron-variant | SENP2 | GRCh38.p7 | 3:185601640 | TTTTGTTGTTCTTGC[-/TT]TTTTTTTTTTTTTTT | 59343 |
| rs397749469 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616790 | AAAAAAAAAAAAAAA[-/A]CGTTTAAAGTGGAAA | 59343 |
| rs397874085 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185629590 | CAAAAAAAAAAAAAA[-/A]GTGCTTATGGTACAT | 59343 |
| rs397875508 | in-del | -/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592634 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 59343 |
| rs397875536 | in-del | -/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616810 | AAAGTGGAAATCAGG[-/G]AGTTTACTATTATGA | 59343 |
| rs398052522 | in-del | -/TTTTTTTTTTTTTTTT | 0.5 | 0 | intron-variant | SENP2 | GRCh38.p7 | 3:185587584 | ATTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTT]GAGAAGGAGTCTCGC | 59343 |
| rs398106834 | in-del | -/A | | | intron-variant | SENP2 | GRCh38.p7 | 3:185621344 | CTAAAAAAAAAAAAA[-/A]TACATGTACCAATAT | 59343 |
| rs527322668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185593190 | AATAGTATGGGAAAG[A/T]TGTGTAAATTCAAGA | 59343 |
| rs527324688 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185584734 | ATTTTTTTTTTTAGT[A/G]GAGATGGGGTTGTCT | 59343 |
| rs527384747 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585475 | GAGACATTAGTGGGC[C/T]GCAGGTTTCATCCTT | 59343 |
| rs527457199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185608513 | ACATTGTTTAAACTC[C/T]CTGTGAAACCCACAA | 59343 |
| rs527558068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185601277 | CTCGAACTCCTGACC[C/T]CAGGTAATCCACCCA | 59343 |
| rs527560359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185592555 | GTACTTATTGAGCAT[A/G]TCTCAGTGCTAACCA | 59343 |
| rs527604294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600408 | TTTAGGTATGTTACC[A/G]GCCAAACATACGGCT | 59343 |
| rs527635893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185610889 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 59343 |
| rs527647864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185602308 | GGGCTAGGAAAGAAA[C/G]TATAAAGTGAGTCTG | 59343 |
| rs527810671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185603028 | AGCGATTCTCCTGCC[G/T]TAGCCTCCTGAGTAG | 59343 |
| rs527852016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185625549 | GGGACTGCCAAGATT[A/G]GGGCAACACAGGCCT | 59343 |
| rs527862950 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185609129 | AAGTTAGTAATTAAT[C/T]CAAAGAAATATTAAA | 59343 |
| rs527977603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185610425 | CCTCAGCCTCCCAGA[C/G]TGCTGGGATTACAGG | 59343 |
| rs528053242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185614282 | AACATACTAATTTTA[A/G]TTGTGATAGGAGAAC | 59343 |
| rs528065404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185618928 | ATATTATTTTGGTGT[A/G]TGTCCTTCAAGTTAA | 59343 |
| rs528187264 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185597784 | TCAGCCTCCTGAATA[C/G]GTGGGATTATAGGGA | 59343 |
| rs528198086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185606667 | GATGCACCAAAAATC[C/T]GCATGCAGCATGTGC | 59343 |
| rs528246057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185628503 | GGAGTGCCTCAATAA[C/T]GTGAACTTCTTTTTT | 59343 |
| rs528265820 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185591878 | TTGGTTGGGCCTACA[A/G]GCACGTTATCACACC | 59343 |
| rs528268394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185620954 | GACCAGCCTGGGCAA[C/T]ATGGAAAGACCCTGT | 59343 |
| rs528305030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628001 | ATAAAGGCATTTATT[A/G]CTTAGTCTCAGCAGT | 59343 |
| rs528414601 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185616952 | TCTCTATAAAATGAT[A/G]ATAATGTCTTCCTCA | 59343 |
| rs528430844 | snp | C/T | 1.763e-05 | 0.00296895 | intron-variant | SENP2 | GRCh38.p7 | 3:185621777 | GAAGTAAAATTCTCA[C/T]TCCTCTTACATTTAA | 59343 |
| rs528434074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185623246 | TCCCGGGTTCAAGAG[A/G]TTCTCCTGCCTCAGC | 59343 |
| rs528554614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185616047 | TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC | 59343 |
| rs528569085 | in-del | -/TCAGCCTAGACGA | 0.00279162 | 0.0372561 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585191 | AGTGATCGTCTCACC[-/TCAGCCTAGACGA]TCAGCCTACCAAGTA | 59343 |
| rs528590449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185615535 | TTTTAGTAGAGACCG[A/G]GTTTCACCATGTTGG | 59343 |
| rs528762506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185591416 | GAGTGTAGTGGTGCA[A/G]TCTCGACTCACTGCA | 59343 |
| rs528820283 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185629118 | AAATAAATACGTTTT[C/T]CTCATAAAAAAACAG | 59343 |
| rs528866664 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP2 | GRCh38.p7 | 3:185616732 | GTAAGCCGAGATGGC[A/G]CCACTGCACTCCGGC | 59343 |
| rs528884045 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185607075 | CAACCTCTGTCTCCC[A/G]CGTTCCAGCATATGT | 59343 |
| rs528967051 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP2 | GRCh38.p7 | 3:185591459 | CGGGTTCACACCATT[C/G]TCCTGCCTCAGCCTC | 59343 |
| rs529003748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185591079 | CTGGCTAGTTTTTTT[G/T]TATTTTTAGTAGAGA | 59343 |
| rs529047344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622761 | GGGATCATACAGTAT[A/T]GTTTGATGTGCTGCT | 59343 |
| rs529083794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628761 | TATGCCCACCTTGGC[C/T]TCCCAAAGTGCTGGG | 59343 |
| rs529090998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622033 | CTTAGCATGCATTTT[A/T]TTTTTAAAATAATAG | 59343 |
| rs529194431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185606767 | CAAGGCCTATAGCGG[C/T]CACGTGTGCTCAGTG | 59343 |
| rs529217167 | in-del | -/TCT | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185619194 | ACAGTCTTTTTATCC[-/TCT]TCTTTAGTACCTTAC | 59343 |
| rs529233640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185614453 | CACTTGGGGGATTTG[C/G]TAATTCTCTTTTCTT | 59343 |
| rs529240655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185616189 | TAAAAGTTTAAAGGC[A/G]AGAATGGGCGTGGTG | 59343 |
| rs529341486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600540 | AAAGCCTGCCAGTGA[A/G]TTCTGTTATTACCTA | 59343 |
| rs529488793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185629580 | GACTCCATCTCAAAA[A/G]AAAAAAAAAAGTGCT | 59343 |
| rs529634849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185623304 | TGCCACCACGCCCGG[A/C]TAATTTTGTATTTTT | 59343 |
| rs529655943 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630354 | GAACTCTCACTGGGG[G/T]CGGAAGGAAGTGGAG | 59343 |
| rs529692579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185627328 | TAGCAAGGGAAAAAT[C/T]GGCCTGTGAGAACTG | 59343 |
| rs529765271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185620779 | GGAAAGAGTCTTAGT[A/G]TGCATAAGGGTTATT | 59343 |
| rs529886935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185587217 | GGCTTACCGCAACCT[C/T]CGCCTCCTGGGTTCA | 59343 |
| rs529924901 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592320 | GCCCTTCCAAAGTGC[C/T]GGGATTATGGATATG | 59343 |
| rs529924944 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185624794 | AATCACTTGAACCCG[A/G]TAGGCAGAGGTTGCA | 59343 |
| rs529986948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185626706 | TGAACCCAGGAGGTG[A/G]AGGTTGCAGTGAGCC | 59343 |
| rs530064222 | snp | A/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185595241 | TTTAGTAGCCACAAT[A/T]TGCTATGTTACCAAG | 59343 |
| rs530181447 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185604085 | GAGATTGGGCCACTG[C/T]GCTCCAGCCTGGGCG | 59343 |
| rs530255691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628556 | TTGTTGCCCAGGCTG[G/T]AGTGCAATGGCGCAA | 59343 |
| rs530265784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185605043 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCGAATC | 59343 |
| rs530402227 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP2 | GRCh38.p7 | 3:185589632 | ATGTGAAAAGCCTAC[C/T]ATAGAATAGCATTCT | 59343 |
| rs530440612 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185595043 | CTCATGACCTTAAAG[A/G]TGAAAGAGATTTTAA | 59343 |
| rs530446989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185596527 | TCAGGAGACTGAGGT[A/G]GGAGGATCACTTGAG | 59343 |
| rs530461655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185628290 | TACAGGCATGTACCA[C/T]CATGCCTGGCTAATT | 59343 |
| rs530539296 | snp | C/G | 4.96101e-05 | 0.00498022 | intron-variant | SENP2 | GRCh38.p7 | 3:185613425 | TAAGTAAAAATCCTA[C/G]TTACATTTGATACCT | 59343 |
| rs530539995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185605140 | TTTGGGAGGCTGAAG[C/T]GCGTGGATCACCTGA | 59343 |
| rs530623403 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185619779 | GTTGCCCAGGCTGGA[A/G]TGAACTGGTGTGATC | 59343 |
| rs530694295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185627475 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTA | 59343 |
| rs530821144 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185627986 | TAATTCCAGTAAAAA[A/C]TAAAGGCATTTATTG | 59343 |
| rs530825358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185628587 | TCTCAGCTCACTGCA[A/G]CCTCCGCCTCCCGGG | 59343 |
| rs530831134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185620807 | ATTTATATTTATTTA[A/G]TTTTGTTTACAAGAT | 59343 |
| rs530905590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185623211 | CAATGGCGTGATCTC[A/G]GCTCACCGCAACCTC | 59343 |
| rs531093944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185590930 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 59343 |
| rs531362189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185601479 | AAATTATAAGTGTAC[A/G]TGGCCTGGTTAATTT | 59343 |
| rs531380935 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586236 | CGTCAGGAGTGGTGG[C/T]GGGCGGGGGCCTCTG | 59343 |
| rs531387111 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185600728 | CTGTTTGCAAGTGAT[C/T]TTTCATTTTACAATT | 59343 |
| rs531390613 | snp | A/C | | | intron-variant | SENP2 | GRCh38.p7 | 3:185614281 | AAACATACTAATTTT[A/C]ATTGTGATAGGAGAA | 59343 |
| rs531488952 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585805 | AACTGGCTTAAGACT[C/G]TCTGTCACACGCCAT | 59343 |
| rs531530289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185593310 | AGACAGGGTCTTGCT[A/G]TATTGCTCAGGCTGA | 59343 |
| rs531565070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185594944 | GGCCAGGCTGGTCTT[C/G]AACTCCTGACCTCAA | 59343 |
| rs531617084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185593889 | GCCCACCACTATGCC[C/T]GGCTAATTTTTGTGT | 59343 |
| rs531695067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185603740 | GGGTGAACTTATTTT[A/C]TAAGCATTTAATGCT | 59343 |
| rs531734127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185587424 | AGGCATGAGCCACTG[C/T]ACTCAGCCCCAAAAG | 59343 |
| rs531852710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185595900 | CTACCTCCCGGGTTC[C/T]AACGATTCTTCTGCT | 59343 |
| rs531901766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185619031 | GTGATACAGTTATGT[A/G]GATCTTTCCATTATT | 59343 |
| rs531937674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185626501 | TAGCTGGCCAGGCGT[A/G]GTGGCTCACACCTGT | 59343 |
| rs531954802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185626579 | GGAGTTCAAGACCAG[C/T]CTGGCCAACATGGTG | 59343 |
| rs531990968 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185587208 | TGCGATCTCGGCTTA[-/C]CGCAACCTCCGCCTC | 59343 |
| rs532074337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185610953 | ACAGATCGAGACTCC[A/G]TCTCAAAATAAATAA | 59343 |
| rs532075236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185620065 | TTTCTTTTTTTTTTT[A/T]AAATTTTTATTTTTA | 59343 |
| rs532107102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185611097 | CCTGACCAACATGGC[A/G]AAACCCCATGTCTAC | 59343 |
| rs532113291 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP2 | GRCh38.p7 | 3:185627238 | GGCACAATTTGCAAA[C/T]CTCTGAACTGTGGCA | 59343 |
| rs532175953 | snp | C/T | 1.6504e-05 | 0.00287258 | missense | SENP2 | GRCh38.p7 | 3:185614658 | TACTCAGGAGGAAAG[C/T]GTCAATAATTGAGAC | 59343 |
| rs532186347 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185627863 | TCATCCACAGACCTT[A/G]TTTTGATAGATGTTG | 59343 |
| rs532216578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185594107 | ATCTTTTTTTTTTAA[A/G]CCAAAAAAGGAAGTC | 59343 |
| rs532222068 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185597438 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCCA | 59343 |
| rs532277894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185594696 | ACAATCTCGGTTCAC[C/T]GCAACCTCCACCTCC | 59343 |
| rs532310658 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185586257 | GGGGCCTCTGGTAGC[C/T]CTGGGGACGCTGTAT | 59343 |
| rs532380376 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185605167 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 59343 |
| rs532404381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185587169 | ACGGAGTCTTGCTCT[G/T]TCGCCCAGGCTGGAG | 59343 |
| rs532590771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185596466 | TCTACCAAAAAATCA[A/G]AAAAATTAGCCAGAC | 59343 |
| rs532701070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185611831 | GAAAATTGACATTCA[A/G]GTGTAGATGGTGTAC | 59343 |
| rs532770998 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SENP2 | GRCh38.p7 | 3:185590866 | GAGCGACACTCCATC[-/T]CAAAAAAAAAAAAAA | 59343 |
| rs532882268 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185601504 | TAATTTTCATACACT[A/G]GTCATATCCATCAGT | 59343 |
| rs532892251 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185602982 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 59343 |
| rs532999667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185600294 | AGTCAGAGAAGCCCA[C/G]GTATTCCTAGGGCAG | 59343 |
| rs533014639 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SENP2 | GRCh38.p7 | 3:185619709 | TTATTCTTTAAAAAA[-/T]TTTATGTTTATTTTA | 59343 |
| rs533065146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185592415 | GATTAAAGGAAAAAG[G/T]CATAGTAAAATGCTA | 59343 |
| rs533097083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185607557 | CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC | 59343 |
| rs533134925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185609392 | TTGCTAGGCATCTTT[C/T]GTTTGTTTGTTTTTG | 59343 |
| rs533237698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185608346 | TCTAGAAATATTGGT[A/G]GGTAGTATTAGCAAG | 59343 |
| rs533266377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185601615 | TCTAATTTTCCCATA[C/T]ATTCTCTCCTTTTGT | 59343 |
| rs533317313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185618259 | TGTTTTATTTTTTGA[G/T]TAATAAAGGGATATA | 59343 |
| rs533488680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185610317 | AGGCGTCCACCGCCA[C/T]GCCCAGCTAATTTTT | 59343 |
| rs533540936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185624156 | CTAGATTTGGCTCCC[A/T]TCCTGCCCTTCCTCC | 59343 |
| rs533549089 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185615846 | CCCTTAGATGTCCTA[A/G]TCTTATTTTGATGTT | 59343 |
| rs533577109 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP2 | GRCh38.p7 | 3:185630426 | TTTTTTTTGTTTTTG[G/T]TTTTTTGAGGCTCAA | 59343 |
| rs533603592 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585237 | GCGTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 59343 |
| rs533749799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185623625 | CTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAC | 59343 |
| rs533772025 | snp | C/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185603342 | TTCAAATGTATTGCA[C/T]TGAGAAAGACATCAT | 59343 |
| rs533911864 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185605435 | ATCAGGAAATTAACA[C/G]TGATATAATACTATT | 59343 |
| rs533915868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185615816 | TTCTCTTCATGTCAA[A/G]AAGGATGGTGTGACC | 59343 |
| rs533936670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185591246 | CTTATCTTTTCTAGA[A/G]GTAACTACTGTTACC | 59343 |
| rs533950612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599584 | CTGCCACTCAGGAAG[C/G]CTTGTAAAGTTGGGG | 59343 |
| rs534013901 | snp | G/T | 1.65485e-05 | 0.00287645 | utr-variant-5-prime | SENP2 | GRCh38.p7 | 3:185586398 | GTGTCGGCCGCCGCT[G/T]CTGCTTGGGCCTGGT | 59343 |
| rs534052585 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP2 | GRCh38.p7 | 3:185585897 | AAGGGCGCCTAAAAC[A/G]GTAAACGTGTGTTAA | 59343 |
| rs534098641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185608830 | CTGGAAAAGTGTCTA[C/T]TAAATGTAGCCATAG | 59343 |
| rs534260030 | snp | C/T | 1.65004e-05 | 0.00287227 | intron-variant | SENP2 | GRCh38.p7 | 3:185600889 | CTGTAAATGGAAACT[C/T]AGCATTTATTAGGTG | 59343 |
| rs534389360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185590460 | GGCTGAGGCAGGAGA[A/G]TCGCTTGAACCTGGG | 59343 |
| rs534492374 | in-del | -/GACTTA | 0.00119737 | 0.0244387 | intron-variant | SENP2 | GRCh38.p7 | 3:185599235 | CAGTGTCCTCAATGT[-/GACTTA]GATCAAGGTCATATT | 59343 |
| rs534524228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185609493 | GCCTGGATATTTATC[A/T]AGTAATGGATAATAT | 59343 |
| rs534807206 | snp | A/G | 4.95021e-05 | 0.0049748 | intron-variant | SENP2 | GRCh38.p7 | 3:185599055 | ATATTTCTGTTTCCC[A/G]CTACCTCCTTCTGCC | 59343 |
| rs534818367 | snp | C/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185613421 | AGTGTAAGTAAAAAT[C/G]CTAGTTACATTTGAT | 59343 |
| rs534832667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185606972 | TATCTACTATGTTAT[A/G]TATTTCTTTTTTCCT | 59343 |
| rs534882891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628600 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAAGTCT | 59343 |
| rs534954318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185604176 | ATTTCTATTTTACTT[C/T]CTCTTTGACCTGTGA | 59343 |
| rs534980872 | snp | A/G | 3.30224e-05 | 0.00406326 | missense | SENP2 | GRCh38.p7 | 3:185606370 | AATAGAAGACCAGGT[A/G]GCCGTCGCCATAGCA | 59343 |
| rs535012983 | snp | A/G | | | intron-variant | SENP2 | GRCh38.p7 | 3:185590415 | TAGCTTGCTGTGGTG[A/G]CAGGAGCTTGTAATC | 59343 |
| rs535066800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185590560 | TCAGGAAAAAAAAAA[A/C]CAAAAAAACTTAAGT | 59343 |
| rs535165933 | snp | G/T | | | intron-variant | SENP2 | GRCh38.p7 | 3:185592839 | CCAGGCTGGTCTCAA[G/T]CTCCTGACCTCAAGT | 59343 |
| rs535233195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628418 | CTGGGATTACAGGCA[A/T]GTGCCACCACGCCCG | 59343 |
| rs535380448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185597847 | TTAGTAGAGATGGGG[C/T]TTCTCCATGTTAGTC | 59343 |
| rs535461552 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP2 | GRCh38.p7 | 3:185615569 | GGCTGGTCTCGAACT[C/T]CTGACCTTAGATGAT | 59343 |
| rs535463375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185607217 | TATATGTATTCTTCT[A/G]TAGATATTCTATATA | 59343 |
| rs535572752 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP2 | GRCh38.p7 | 3:185592001 | CTGTCTTTAAGAACC[A/G]GTAATATTTCTTTTT | 59343 |
| rs535584008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185628640 | GCCTCCCAAGTAACC[A/G]TGATTACAGGAATGC | 59343 |
| rs535607060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185599752 | GAGCAAAGGAGAATA[A/C]ATACATACCCCTGTG | 59343 |
| rs535644417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185622977 | TTCCGTCACTATGCC[C/T]GGCTAATTTTTGAAT | 59343 |
| rs535681025 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP2 | GRCh38.p7 | 3:185629197 | TGCCTATTGTGCCAC[C/G]ACGTGGATATTTGCA | 59343 |
| rs535736932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185589843 | ATTTTTTATTTATTT[A/T]TTTATCGTAGAGATG | 59343 |
| rs535775156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP2 | GRCh38.p7 | 3:185597032 | CTAATTTTTGTATTT[G/T]TTTTAGAGACGGGAT | 59343 |