SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2358 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | PARK2 | GRCh38.p7 | 6:162227882 | TGAAATTTGGGGGAA[A/G]TCCAAAAAGATGGAC | 5071 |
rs25622 | in-del | -/TTTTG | 0 | 0 | intron-variant | PARK2 | GRCh38.p7 | 6:161647855 | CTTTGCATGCTCTTA[-/TTTTG]TTTTAATAAATTATC | 5071 |
rs140855 | in-del | -/AC/CA | 0 | 0 | intron-variant | PARK2 | GRCh38.p7 | 6:161512358 | GGCTCTGGTGCATAA[-/AC/CA]GACAATATAATAAAA | 5071 |
rs475158 | snp | C/G | 0.460589 | 0.13473 | intron-variant | PARK2 | GRCh38.p7 | 6:161515245 | GTTTTCCCCCTTCCT[C/G]TTATCTGAAAACACA | 5071 |
rs475221 | snp | A/G | 0.481165 | 0.0951993 | intron-variant | PARK2 | GRCh38.p7 | 6:161537866 | TGGGGAGGCGGCCAC[A/G]GGAAGAGTGAACACA | 5071 |
rs476105 | snp | A/C | 0.429238 | 0.174281 | intron-variant | PARK2 | GRCh38.p7 | 6:161515365 | TTCTTGTGAGTTTTT[A/C]TCCATGTACATATAT | 5071 |
rs476161 | snp | A/C | 0.344815 | 0.231323 | intron-variant | PARK2 | GRCh38.p7 | 6:161521946 | ATTATCAGACATGTA[A/C]TCCATCAGAACAGAG | 5071 |
rs477943 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | PARK2 | GRCh38.p7 | 6:161538162 | CAGCAATAGGCCCGC[C/T]TGACAAATTACCTCC | 5071 |
rs480470 | snp | G/T | 0.519505 | 0.215544 | intron-variant | PARK2 | GRCh38.p7 | 6:161515785 | TCTCAAGGTTCTTCT[G/T]ATGGGATTTTAGTCC | 5071 |
rs480557 | snp | G/T | 0.498611 | 0.0263212 | intron-variant | PARK2 | GRCh38.p7 | 6:161531855 | AGGGATGAGAAGGAT[G/T]AGATTATAAAAGAAC | 5071 |
rs481910 | snp | C/T | 0.42263 | 0.180829 | intron-variant | PARK2 | GRCh38.p7 | 6:161506762 | AATATTGATTTATTA[C/T]ACATTTAATTCTTTA | 5071 |
rs482299 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PARK2 | GRCh38.p7 | 6:161543443 | acatggttaagagga[C/T]ttggaaagggtccat | 5071 |
rs482420 | snp | C/T | 0.345704 | 0.230956 | intron-variant | PARK2 | GRCh38.p7 | 6:161532044 | TCTTCACCATCCTAC[C/T]CTTCCCTGAAACAAA | 5071 |
rs482675 | snp | C/T | 0.362732 | 0.22314 | intron-variant | PARK2 | GRCh38.p7 | 6:161506799 | AGTGTGATATGGCTG[C/T]CCCAAAAAGCTTGCT | 5071 |
rs482845 | snp | A/T | 0.361894 | 0.223562 | intron-variant | PARK2 | GRCh38.p7 | 6:161506854 | TGCAGTACCAAAAAG[A/T]CAATTTGGGGAACCA | 5071 |
rs483366 | snp | C/T | 0.479824 | 0.098392 | intron-variant | PARK2 | GRCh38.p7 | 6:161516100 | CATTACTTTTTTCTA[C/T]ATAACCTTAAAACAG | 5071 |
rs487775 | snp | C/T | | | intron-variant | PARK2 | GRCh38.p7 | 6:161537436 | ACAATGCTTCAAGTT[C/T]TTTtttttttctttt | 5071 |
rs490167 | snp | A/G | 0.457853 | 0.138915 | intron-variant | PARK2 | GRCh38.p7 | 6:161522881 | ATCAATAAAGAAATA[A/G]GTAACATTAGATGAC | 5071 |
rs490414 | snp | C/T | 0.431621 | 0.171796 | intron-variant | PARK2 | GRCh38.p7 | 6:161513498 | ATCTGCCCGCCTCAG[C/T]CTCCCAGAGTGCTGG | 5071 |
rs492267 | snp | A/G | 0.357238 | 0.225832 | intron-variant | PARK2 | GRCh38.p7 | 6:161518539 | GAGAGCTGAACCGAG[A/G]CTCACATCTGCCCTT | 5071 |
rs493806 | snp | C/T | 0.360632 | 0.224189 | intron-variant | PARK2 | GRCh38.p7 | 6:161493848 | TGAACAGTGAAGTCC[C/T]TCAATTAGCATTCCT | 5071 |
rs495991 | snp | A/G | 0.328616 | 0.237317 | intron-variant | PARK2 | GRCh38.p7 | 6:161534405 | GTGCTGAATGCAGGC[A/G]TCGTTGCTGAGGATA | 5071 |
rs496759 | snp | C/T | 0.344815 | 0.231323 | intron-variant | PARK2 | GRCh38.p7 | 6:161528458 | CCACCAGCACCCCAG[C/T]GAAAATGGGAAATAA | 5071 |
rs497002 | snp | A/G | 0.362732 | 0.22314 | intron-variant | PARK2 | GRCh38.p7 | 6:161500853 | aaaactaaactaaac[A/G]tacgcttaccatatg | 5071 |
rs503783 | snp | C/T | 0.449599 | 0.150533 | intron-variant | PARK2 | GRCh38.p7 | 6:161538617 | CTTCAACTGGTAGAA[C/T]CCTGGGGCCCACTGA | 5071 |
rs503890 | snp | C/T | 0.343924 | 0.231686 | intron-variant | PARK2 | GRCh38.p7 | 6:161522627 | GCTTCGAGAAGTACA[C/T]GACAGAAGACATTCT | 5071 |
rs505319 | snp | C/T | 0.459914 | 0.13578 | intron-variant | PARK2 | GRCh38.p7 | 6:161520761 | GATAAAAGAGAAATC[C/T]AATGCTGATGAGTAG | 5071 |
rs505555 | snp | G/T | 0.347253 | 0.230308 | intron-variant | PARK2 | GRCh38.p7 | 6:161532253 | TTTGCCTAGAGACTG[G/T]GATTTGTGTAAAACT | 5071 |
rs505693 | snp | C/T | 0.346147 | 0.230772 | intron-variant | PARK2 | GRCh38.p7 | 6:161522819 | GGTACTTCCCTTCTA[C/T]CTCAATCCCATCACA | 5071 |
rs505845 | snp | A/G | 0.362104 | 0.223456 | intron-variant | PARK2 | GRCh38.p7 | 6:161506827 | GCTCAGTTGTAAACT[A/G]GGCCATTGGTCTGCA | 5071 |
rs506428 | snp | G/T | 0.497473 | 0.0354532 | intron-variant | PARK2 | GRCh38.p7 | 6:161532326 | AAGCAAAAAAATAAC[G/T]TTTTCATTGGTAAAA | 5071 |
rs507499 | snp | C/T | 0.351635 | 0.228408 | intron-variant | PARK2 | GRCh38.p7 | 6:161523003 | GCAAGACAAAATAAA[C/T]GGAAGCCCTTTAAAT | 5071 |
rs508144 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PARK2 | GRCh38.p7 | 6:161543931 | AAAGTTTGTGAGATA[A/G]TTCTGATGAATAGCA | 5071 |
rs508517 | snp | A/T | 0.361894 | 0.223562 | intron-variant | PARK2 | GRCh38.p7 | 6:161507293 | GAGTGACTTTTTGTC[A/T]AAGTATCTTTTCAGT | 5071 |
rs508605 | snp | C/T | 0.361894 | 0.223562 | intron-variant | PARK2 | GRCh38.p7 | 6:161507324 | GTGGCATTTGTAACA[C/T]TGCTCATCTCTATGA | 5071 |
rs509205 | snp | A/T | 0.431916 | 0.171483 | intron-variant | PARK2 | GRCh38.p7 | 6:161516599 | TTGGGAGGCCGAGAC[A/T]GGTGGATCACCTGAG | 5071 |
rs509315 | snp | A/G | 0.462253 | 0.132093 | intron-variant | PARK2 | GRCh38.p7 | 6:161516644 | ACCAGCCTGGCCAAC[A/G]TGGTAAAACTCCATC | 5071 |
rs509495 | snp | A/T | 0.298905 | 0.24517 | intron-variant | PARK2 | GRCh38.p7 | 6:161549199 | TATGGTTCAATGCAG[A/T]AAAAGTCTACCAAAT | 5071 |
rs510849 | snp | C/T | 0.453818 | 0.144769 | intron-variant | PARK2 | GRCh38.p7 | 6:161521373 | AAGCAAAGCATAAAA[C/T]TAGGATAGAAATCCC | 5071 |
rs510968 | snp | C/T | 0.35809 | 0.225425 | intron-variant | PARK2 | GRCh38.p7 | 6:161532822 | TGTCACTGTCCACCC[C/T]TTATACCTGCCACCA | 5071 |
rs513141 | snp | C/T | 0.365646 | 0.221644 | intron-variant | PARK2 | GRCh38.p7 | 6:161507841 | GCCTGAATCACTCCC[C/T]GACCACCCAAGTAAG | 5071 |
rs515801 | snp | A/T | 0.364817 | 0.222075 | intron-variant | PARK2 | GRCh38.p7 | 6:161504087 | CCGATGACATGGGTA[A/T]AGAGACAGAAGATGT | 5071 |
rs515878 | snp | C/T | 0.364609 | 0.222182 | intron-variant | PARK2 | GRCh38.p7 | 6:161504112 | AGATGTGACTTCTTA[C/T]AGTTAGAGGTCAAAA | 5071 |
rs517010 | snp | G/T | 0.481009 | 0.0955756 | intron-variant | PARK2 | GRCh38.p7 | 6:161514134 | AAATAAACAATAGAT[G/T]TAAAGAACAAATGAC | 5071 |
rs517656 | snp | C/T | 0.423413 | 0.180077 | intron-variant | PARK2 | GRCh38.p7 | 6:161504306 | CTGAGGAAGAGCCGG[C/T]AGGGATTGCCATGGG | 5071 |
rs517658 | snp | A/G | 0.361684 | 0.223667 | intron-variant | PARK2 | GRCh38.p7 | 6:161504307 | TGAGGAAGAGCCGGC[A/G]GGGATTGCCATGGGG | 5071 |
rs518666 | snp | A/G | 0.328616 | 0.237317 | intron-variant | PARK2 | GRCh38.p7 | 6:161523739 | AATCAATTTCATGGA[A/G]AGTAAGTATTTATCT | 5071 |
rs520732 | snp | A/G | 0.358515 | 0.225221 | intron-variant | PARK2 | GRCh38.p7 | 6:161514559 | AAGGTGACAAAAAGC[A/G]AGAGAGGGTTAAGGA | 5071 |
rs521641 | snp | A/G | 0.35809 | 0.225425 | intron-variant | PARK2 | GRCh38.p7 | 6:161514644 | CTGGAGTTGGGGGAT[A/G]GCCGTTTGTCCTGAT | 5071 |
rs523179 | snp | C/T | 0.427879 | 0.175668 | intron-variant | PARK2 | GRCh38.p7 | 6:161519576 | GCTGGAGATCAGGAA[C/T]AGGCAGGTGTGATGG | 5071 |
rs523995 | snp | A/G | 0.35894 | 0.225016 | intron-variant | PARK2 | GRCh38.p7 | 6:161494863 | GTTCTTCTAGGATTC[A/G]TCCCCAGCCTTTCCC | 5071 |
rs526020 | snp | A/T | 0.427727 | 0.175821 | intron-variant | PARK2 | GRCh38.p7 | 6:161519897 | TGTCATTCAGTCTGA[A/T]ACCACCTCAAAGAAG | 5071 |
rs526207 | snp | A/G | 0.365853 | 0.221536 | intron-variant | PARK2 | GRCh38.p7 | 6:161503923 | GACACCCTAGACAGG[A/G]GGAAAGCATTGAAGA | 5071 |
rs527960 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | PARK2 | GRCh38.p7 | 6:161542383 | GTACCTCAAAATCAC[A/G]GAACACTTTCTAGGA | 5071 |
rs528061 | snp | G/T | 0.364609 | 0.222182 | intron-variant | PARK2 | GRCh38.p7 | 6:161504120 | CTTCTTATAGTTAGA[G/T]GTCAAAAAGCCATAA | 5071 |
rs530128 | snp | C/T | 0.181978 | 0.240568 | intron-variant | PARK2 | GRCh38.p7 | 6:161539183 | TAACGTAAGAACTAT[C/T]TAAACTATTTAAACA | 5071 |
rs531449 | snp | C/G | 0.356811 | 0.226034 | intron-variant | PARK2 | GRCh38.p7 | 6:161518529 | GGCTCTGGGTGAGAG[C/G]TGAACCGAGGCTCAC | 5071 |
rs536667 | snp | A/G | 0.359152 | 0.224913 | intron-variant | PARK2 | GRCh38.p7 | 6:161532545 | ATTTTCAATGTCTCT[A/G]GAACATTTAACATTA | 5071 |
rs537738 | snp | C/T | 0.495671 | 0.0463237 | intron-variant | PARK2 | GRCh38.p7 | 6:161532406 | ATACATACACCCACA[C/T]TCATACACACACAGC | 5071 |
rs539455 | snp | C/T | 0.362313 | 0.223351 | intron-variant | PARK2 | GRCh38.p7 | 6:161500228 | ctctcccctctcccc[C/T]atacatgcacagcct | 5071 |
rs541480 | snp | G/T | 0.365439 | 0.221752 | intron-variant | PARK2 | GRCh38.p7 | 6:161508606 | gtcccttaatacact[G/T]aataaatccgccctg | 5071 |
rs543888 | snp | A/G | 0.357664 | 0.225629 | intron-variant | PARK2 | GRCh38.p7 | 6:161528022 | ATTTCTATCTTTTCT[A/G]TCTTTTCAATCTCAG | 5071 |
rs545310 | snp | C/T | 0.357664 | 0.225629 | intron-variant | PARK2 | GRCh38.p7 | 6:161514896 | TACTACGGAGTCCTC[C/T]GGGTTCCTCTCCCCT | 5071 |
rs545749 | snp | A/G | 0.422787 | 0.180679 | intron-variant | PARK2 | GRCh38.p7 | 6:161500919 | ctccctctgtcgccc[A/G]ggctggagtgcaatg | 5071 |
rs548060 | snp | A/G | 0.428937 | 0.17459 | intron-variant | PARK2 | GRCh38.p7 | 6:161515202 | ATCTATTATATGCAT[A/G]GTACCAACGAGAAAT | 5071 |
rs551770 | snp | A/G | 0.462253 | 0.132093 | intron-variant | PARK2 | GRCh38.p7 | 6:161515592 | TTGAAACAGTATATC[A/G]TTATGCTACTATGAT | 5071 |
rs551941 | snp | A/G | 0.35809 | 0.225425 | intron-variant | PARK2 | GRCh38.p7 | 6:161510987 | TCTTCCAATATGGAA[A/G]ATGCTATTTTTAAAG | 5071 |
rs551962 | snp | A/G | 0.460813 | 0.134379 | intron-variant | PARK2 | GRCh38.p7 | 6:161515654 | AAGCATTGAATAAAT[A/G]AAGTTAAAATTGAGT | 5071 |
rs555637 | snp | C/T | 0.449345 | 0.150869 | intron-variant | PARK2 | GRCh38.p7 | 6:161493627 | AGGGCACAGATTACA[C/T]GAAGAGCAGATGCAG | 5071 |
rs558209 | snp | A/G | 0.34101 | 0.232846 | intron-variant | PARK2 | GRCh38.p7 | 6:161521151 | CAGTGTCAGAGTTGG[A/G]GGTGAGTCTTAGGTT | 5071 |
rs561275 | snp | G/T | | | intron-variant | PARK2 | GRCh38.p7 | 6:161532166 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 5071 |
rs565301 | snp | A/G | 0.48666 | 0.0805725 | intron-variant | PARK2 | GRCh38.p7 | 6:161500342 | cagcaccaggagtga[A/G]cctcatgtaaactga | 5071 |
rs568670 | snp | C/T | 0.436408 | 0.16659 | intron-variant | PARK2 | GRCh38.p7 | 6:161541089 | AGTTTGCAAATGTTA[C/T]TCCTTGGACAGACGT | 5071 |
rs568893 | snp | A/C | 0.490997 | 0.0664859 | intron-variant | PARK2 | GRCh38.p7 | 6:161507740 | ATTTAATCCCATTTT[A/C]GGTGGTATTTCATAT | 5071 |
rs569463 | snp | C/T | 0.46137 | 0.133501 | intron-variant | PARK2 | GRCh38.p7 | 6:161517187 | GCACATTTTCAATCA[C/T]GAGTTCATGATTGAC | 5071 |
rs569645 | snp | A/G | 0.476401 | 0.106032 | intron-variant | PARK2 | GRCh38.p7 | 6:161507771 | TTTCCTACCCTCACT[A/G]AAACCTCCTTAAACA | 5071 |
rs569646 | snp | A/C | 0.476314 | 0.106217 | intron-variant | PARK2 | GRCh38.p7 | 6:161507772 | TTCCTACCCTCACTA[A/C]AACCTCCTTAAACAT | 5071 |
rs571496 | snp | C/T | 0.430732 | 0.172731 | intron-variant | PARK2 | GRCh38.p7 | 6:161517462 | GTTGAGGTGCTAggc[C/T]gggcgtggtggctca | 5071 |
rs572290 | snp | A/G | 0.421368 | 0.182025 | intron-variant | PARK2 | GRCh38.p7 | 6:161517516 | gaggccaaagcaggc[A/G]gatcacaaggtcagg | 5071 |
rs574165 | snp | C/T | 0.493013 | 0.058691 | intron-variant | PARK2 | GRCh38.p7 | 6:161535643 | AACATCGTACTCGTA[C/T]TCCGACAGAGAAAAG | 5071 |
rs576613 | snp | A/G | 0.493386 | 0.0571263 | intron-variant | PARK2 | GRCh38.p7 | 6:161516016 | GTAGTGCCTATAATT[A/G]TTAAAAATAACCATC | 5071 |
rs577876 | snp | A/G | 0.485324 | 0.0843964 | intron-variant | PARK2 | GRCh38.p7 | 6:161502123 | TGGATCACATGAAGC[A/G]ACTCTGAAATGCATT | 5071 |
rs693282 | snp | A/G | 0.425586 | 0.17796 | intron-variant | PARK2 | GRCh38.p7 | 6:161502506 | CTGAAGCAACATCCC[A/G]ACTCTGGAATCCATT | 5071 |
rs713053 | snp | A/G | 0.436834 | 0.166111 | intron-variant | PARK2 | GRCh38.p7 | 6:162150231 | ACAGTGAAAAGGATC[A/G]GTCACAGCAATAACT | 5071 |
rs713054 | snp | A/G | 0.499954 | 0.00479211 | intron-variant | PARK2 | GRCh38.p7 | 6:162150323 | TGATGTGAATTTAAA[A/G]TGTCTGAGTTTGGGG | 5071 |
rs713055 | snp | C/T | 0.499998 | 0.000998401 | intron-variant | PARK2 | GRCh38.p7 | 6:162150291 | TGTATCCTAAGAAGA[C/T]AGTGGCAAAATGTTT | 5071 |
rs713056 | snp | A/T | 0.437965 | 0.164831 | intron-variant | PARK2 | GRCh38.p7 | 6:162150349 | TGGGGGCCTTCTCTG[A/T]TTCTGCTCCTGATTT | 5071 |
rs717980 | snp | C/T | | | intron-variant | PARK2 | GRCh38.p7 | 6:161909552 | TAGAGTAATAGGGCC[C/T]GAGGAACTCATAGAA | 5071 |
rs718319 | snp | A/G | 0.14933 | 0.228835 | intron-variant | PARK2 | GRCh38.p7 | 6:161466593 | GCATATTAAAAGATA[A/G]GCCAGTACATCTCTG | 5071 |
rs719650 | snp | A/G | 0.489259 | 0.0724914 | intron-variant | PARK2 | GRCh38.p7 | 6:162647409 | ACCCAAATAAAATGA[A/G]TGTTAAGATTTGTTA | 5071 |
rs724790 | snp | A/G | 0.357451 | 0.225731 | intron-variant | PARK2 | GRCh38.p7 | 6:162534567 | AGTTATTCAATATAC[A/G]CTGACTGAATATATT | 5071 |
rs732434 | snp | A/G | 0.338523 | 0.233803 | intron-variant | PARK2 | GRCh38.p7 | 6:162354809 | ACGTCAACTTATTCA[A/G]TTAATGGTTTGCTGA | 5071 |
rs732435 | snp | C/T | 0.335101 | 0.23507 | intron-variant | PARK2 | GRCh38.p7 | 6:162354823 | ATATAAAAGCTAATA[C/T]GTCAACTTATTCAAT | 5071 |
rs737631 | snp | C/T | 0.337614 | 0.234145 | intron-variant | PARK2 | GRCh38.p7 | 6:161741401 | CCTTGGTGTCAACTC[C/T]GTTCAGTTTCCTTGC | 5071 |
rs737715 | snp | C/T | 0.130008 | 0.219321 | intron-variant | PARK2 | GRCh38.p7 | 6:161569031 | ACTTAGGAATGTCTA[C/T]GACCATCGATCCCTC | 5071 |
rs741982 | snp | A/C | 0.465788 | 0.126237 | intron-variant | PARK2 | GRCh38.p7 | 6:162441236 | TCCTTCTATGGCATG[A/C]CATTTTTCTCTAGTT | 5071 |
rs742769 | snp | C/T | 0.392696 | 0.205275 | intron-variant | PARK2 | GRCh38.p7 | 6:161596142 | ATCAGGGTTGAGGAC[C/T]CATTTTTGTGTTTCG | 5071 |
rs742770 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PARK2 | GRCh38.p7 | 6:161596172 | GACACATTCTTGGCA[C/T]GTTCCCCTTGAGCAT | 5071 |
rs742771 | snp | A/G | 0.350109 | 0.229081 | intron-variant | PARK2 | GRCh38.p7 | 6:161596556 | CCTCCATTCATGTCT[A/G]CCTTGCCTTTCACCC | 5071 |
rs742772 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PARK2 | GRCh38.p7 | 6:161603717 | GGGAAGTAGCAGATA[C/T]ATGGAACTTCTTCAG | 5071 |