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 |