SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7073 | snp | C/T | 0.450231 | 0.149691 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870357 | AGCCGGCCAGCCAGA[C/T]GTGTGCCTGAATGCC | 11252 |
rs7074 | snp | A/C | 0.450357 | 0.149522 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869821 | TTAACAGTTCCTTTA[A/C]ATGTGTAGTATTTGA | 11252 |
rs8569 | snp | A/G | 0.40086 | 0.199352 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870768 | TGGCAGATGTTTGAG[A/G]AAAGGAATTATGCCA | 11252 |
rs137567 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928773 | AACAAAATCAATAAA[A/G]CTACACTGAACATAA | 11252 |
rs713717 | snp | C/T | 0.44546 | 0.155869 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000103 | AGAGCTCCTTACTAA[C/T]AACAGCTCACTGCAG | 11252 |
rs713776 | snp | A/G | 0.448836 | 0.15154 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000088 | AGGCAATCTGGTTGC[A/G]GAGCTCCTTACTAAC | 11252 |
rs714003 | snp | C/T | 0.438526 | 0.164189 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973760 | GGCCTGGGCCCATCC[C/T]CCACTCCCGTCTCCA | 11252 |
rs730070 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935423 | TGTGCGGAGACCTAC[C/T]GTGGACATGGCTCCA | 11252 |
rs731950 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947182 | TGGGTCAGGAGGCTG[A/C]CCTTTGTTCAGGTCA | 11252 |
rs732439 | snp | G/T | 0.46754 | 0.123192 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907411 | TTCAGTGAAAAGAAA[G/T]AATTAATGGTAATTT | 11252 |
rs733139 | snp | A/T | 0.427423 | 0.176128 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994077 | CAAATATGAGCTCTC[A/T]AGAAGACCACGATGT | 11252 |
rs737782 | snp | C/G | 0.398714 | 0.200958 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001557 | GCCAGTGCAGTCAGA[C/G]GAGCCCTGAAGTGTG | 11252 |
rs738377 | snp | C/T | 0.427575 | 0.175975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993564 | AAAATGTAAAAGATA[C/T]AATGGTCAAAATTTT | 11252 |
rs738378 | snp | C/T | 0.427423 | 0.176128 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002956 | TTGAAAAGGAAACAG[C/T]GAGGTCAGTTCAAGC | 11252 |
rs738379 | snp | A/C | 0.426047 | 0.177503 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004758 | TACACAGTTGATCCT[A/C]TCTAAAGACCACCCT | 11252 |
rs738380 | snp | C/T | 0.385359 | 0.210185 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004931 | GAAAAGGGAAACAAA[C/T]CAACAAGGCTGTCCT | 11252 |
rs738381 | snp | C/T | 0.44768 | 0.153045 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008101 | GCCTGCTGTGTGCAG[C/T]ACTATCAGCTTCCAT | 11252 |
rs738383 | snp | C/T | 0.465788 | 0.126237 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919387 | CAAATGAGTCATCCC[C/T]GGTCTTTCCAAGGAC | 11252 |
rs738384 | snp | C/T | 0.385168 | 0.210309 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923152 | AGAGTTTTGTACCCA[C/T]GCTACTGGTTTTAAA | 11252 |
rs738385 | snp | C/T | 0.452719 | 0.146304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923314 | gcaaggcagaccaca[C/T]tgctggtcttaagtc | 11252 |
rs738386 | snp | A/G | 0.422158 | 0.181278 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932413 | TCAGTTTTTACCTGT[A/G]TACAGTCTGCTTTCC | 11252 |
rs738387 | snp | A/G | 0.428635 | 0.174898 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933813 | GAAACATTCTTGGAA[A/G]TTATGAATAAGATAT | 11252 |
rs738388 | snp | C/T | 0.443866 | 0.157848 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936316 | GATCATGCGGGGAAA[C/T]ACCTGTCTCTCATCT | 11252 |
rs738389 | snp | C/T | 0.438526 | 0.164189 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936510 | AGGGGACATGAAGCA[C/T]AGGCAAAGGCAAAGG | 11252 |
rs738390 | snp | A/T | 0.298144 | 0.245321 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940225 | AAACTCAAACTCCTT[A/T]ACTACTCAGTAATTA | 11252 |
rs738391 | snp | A/G | 0.438246 | 0.16451 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943872 | TGCACAATACAATAT[A/G]GAAAGCAAAGAAAGA | 11252 |
rs738392 | snp | G/T | 0.439085 | 0.163545 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944273 | AGACATTTGTGTTAG[G/T]CTAAGTCTCTGAGAC | 11252 |
rs738393 | snp | C/T | 0.439085 | 0.163545 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944274 | GACATTTGTGTTAGG[C/T]TAAGTCTCTGAGACT | 11252 |
rs738394 | snp | C/T | 0.438946 | 0.163706 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970890 | TGCAGCGCCTCCCCA[C/T]GCCACCCACAGCTGT | 11252 |
rs738396 | snp | A/G | 0.450609 | 0.149185 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974785 | AGAAAAGAGAAGAAG[A/G]AGGAGGAGGAGGAGG | 11252 |
rs738397 | snp | C/T | 0.424503 | 0.179021 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899265 | CTTTGTGACTTACGG[C/T]ATGGCTCCTTAAACA | 11252 |
rs738537 | snp | A/G | 0.403334 | 0.197456 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881916 | AGGAAGGGAATGCCA[A/G]TGGCCAAAAAGTGAC | 11252 |
rs738538 | snp | A/G | 0.467439 | 0.123371 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885873 | CATGCCCAGCAGAGA[A/G]AGAGCTCCACAGCGC | 11252 |
rs738539 | snp | A/C | 0.414576 | 0.188188 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886795 | TCACTGGCCAGACCA[A/C]AGAGGCAGGGAGGGT | 11252 |
rs742216 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935431 | CATGAGTCTGGAGCC[A/C]TGTCCACAGTAGGTC | 11252 |
rs753086 | snp | C/T | 0.425432 | 0.178112 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870241 | GGTCCGGCTTCTGAC[C/T]GGCCTTTGTCCTGGC | 11252 |
rs760772 | snp | C/T | 0.418653 | 0.184544 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898233 | CAGCACCCCTGCCTT[C/T]TCCAGGCTGTGCCCA | 11252 |
rs875629 | snp | C/T | 0.399968 | 0.200024 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899262 | TACCTTTGTGACTTA[C/T]GGCATGGCTCCTTAA | 11252 |
rs909712 | snp | C/G | 0.451234 | 0.14834 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915219 | GAGAGGCTCAGCACA[C/G]TGGGCAGCCTTTAGG | 11252 |
rs926351 | snp | C/T | 0.437965 | 0.164831 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975170 | ACTGACTCCCTTAAA[C/T]CCAATGCCAATACTC | 11252 |
rs926352 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975457 | TAAAAAATATATACA[A/T]ATATATATATATATA | 11252 |
rs926353 | snp | A/T | 0.437965 | 0.164831 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975501 | GAAAAATTATCCAGC[A/T]GTAAAAATGAATGAA | 11252 |
rs972577 | snp | C/T | 0.43309 | 0.17023 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991639 | GGGAACTCCCAGGTG[C/T]GATAAAGAGAAAGCC | 11252 |
rs972578 | snp | G/T | 0.432651 | 0.170701 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991689 | ACAGTAAACAGTCAT[G/T]AAGAGATCCAAGGGC | 11252 |
rs972579 | snp | C/T | 0.427879 | 0.175668 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991705 | AAGAGATCCAAGGGC[C/T]CAGAACCACAATTCC | 11252 |
rs1040427 | snp | A/C | 0.463774 | 0.129618 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977564 | GCAAAAACAATACAA[A/C]ATCTAGCACTGGTGG | 11252 |
rs1040428 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985193 | ctcagccaggagtgg[C/T]ggcacatgcctgtaa | 11252 |
rs1040430 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985502 | ATGCAGGCCCAGGTC[C/T]AGGTCCAGGAGTGTC | 11252 |
rs1045449 | snp | A/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870072 | CAGGTGCTGCAGCCA[A/G]AGTTACGCGGGGGCC | 11252 |
rs1045585 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869878 | CAGAAATCCTCATTT[C/T]TGTGCTACGGATTTA | 11252 |
rs1062913 | snp | A/G/T | 0.000249093 | 0.0111573 | missense | PACSIN2 | GRCh38.p7 | 22:42879106 | AAGGCCACTGACGGC[A/G/T]TCACCCTGACGGGCA | 11252 |
rs1071960 | snp | C/T | 0.302184 | 0.244493 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953626 | ATTTAAATGCAGTGC[C/T]AAGGGTTTCATTTAA | 11252 |
rs1071961 | snp | A/C | 0.434398 | 0.168811 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953693 | AAGAAACTAAAACTC[A/C]GAGAGGTTAAGTAAT | 11252 |
rs1076117 | snp | A/T | 0.453331 | 0.145452 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903288 | CTGGCAGATGTTGTA[A/T]CCTGTACACACCTGC | 11252 |
rs1076118 | snp | C/T | 0.418814 | 0.184396 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903704 | CTGCAAATGAGGTGA[C/T]GCTATTTACCTTGCA | 11252 |
rs1139852 | snp | C/G | | | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884535 | GTATGAGAAGTCCCT[C/G]AAGGAACTCGACCAG | 11252 |
rs1546860 | snp | C/T | 0.426813 | 0.17674 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004323 | AGAAACTTCAGAACA[C/T]GGGGGCCTGTGCAGA | 11252 |
rs1546861 | snp | A/G | 0.434976 | 0.168179 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959161 | AGGGGTCCTGGAGCG[A/G]TGGCAGGTGATCAGA | 11252 |
rs1569507 | snp | A/G | 0.385359 | 0.210185 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960693 | ACACCCTTCGAAGCC[A/G]GGACAGGGAAGAGAA | 11252 |
rs1569508 | snp | C/T | 0.454544 | 0.143743 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963124 | AAAGACTGGAAACCA[C/T]TGGAcattcattcaa | 11252 |
rs1569509 | snp | A/G | 0.429388 | 0.174127 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963255 | aataaAATGAGGGAC[A/G]TCTCGTGCTGGTTCT | 11252 |
rs1569510 | snp | A/G | 0.434253 | 0.168969 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963442 | CAGGGGGATTCTTTC[A/G]CCCAGCGGTCAGTGC | 11252 |
rs1569511 | snp | C/T | 0.451359 | 0.148171 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948675 | TTTAAGTACAAACCA[C/T]GAGAGGATTTGGTTT | 11252 |
rs1807567 | snp | A/T | 0.402277 | 0.198272 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919622 | TACTAAAAATACAAA[A/T]ATTAGCTGGGTGTGG | 11252 |
rs1807568 | snp | C/T | 0.391583 | 0.206044 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919765 | gtgacagagcaagaa[C/T]ctgtctcaaaaaaaa | 11252 |
rs1807569 | snp | A/G | 0.452597 | 0.146474 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923521 | taagctccgcctccc[A/G]ggttcacgccattct | 11252 |
rs1807570 | snp | C/T | 0.452719 | 0.146304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923552 | cctgcctcagcctcc[C/T]gagtagctgggacta | 11252 |
rs1807571 | snp | C/T | 0.438806 | 0.163867 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971214 | cctcagcctgccaag[C/T]gcctgggattgcagg | 11252 |
rs1807572 | snp | C/G | 0.438946 | 0.163706 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971310 | cgggctggtctccag[C/G]tcccgaccgcaagtg | 11252 |
rs1807573 | snp | G/T | 0.438386 | 0.164349 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972264 | ggttaaatggattaa[G/T]ggcggtgcacgatgt | 11252 |
rs1883313 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008246 | TGTGAGGCTCTAAAA[C/T]TCAGTGGTCTTCTTT | 11252 |
rs1883314 | snp | C/G | 0.459233 | 0.136827 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978801 | AGCATTTCCAAAAAG[C/G]CTGGTCCCTGCCCCT | 11252 |
rs2002595 | snp | G/T | 0.462034 | 0.132445 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900045 | CCAAGACTTCACAGA[G/T]AGCTGAGATGGGGGC | 11252 |
rs2006042 | snp | A/G | 0.424348 | 0.179172 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875072 | agccaggatggtctc[A/G]atctcctgacctcgt | 11252 |
rs2007295 | snp | C/G | 0.0520825 | 0.152737 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947219 | AGGGGCATTCACAGG[C/G]GGCAGAGTGAGCAGG | 11252 |
rs2007395 | snp | A/G | 0.450357 | 0.149522 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875165 | agaccccatctctta[A/G]aaaaaaaaaaaaGTA | 11252 |
rs2010366 | snp | G/T | 0.376592 | 0.215579 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985282 | CAGTGAGCCGAGATC[G/T]CATCACCGCACTCCA | 11252 |
rs2013035 | snp | C/T | 0.0718919 | 0.175435 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42949057 | cagcactttgggagg[C/T]ggaggtggaaggatt | 11252 |
rs2016623 | snp | A/G | 0.438105 | 0.164671 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974543 | ATCCATTAAAAGATC[A/G]TAAGCACCAGCCATG | 11252 |
rs2017874 | snp | A/G | 0.444799 | 0.156695 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907681 | TATTGACATTCGCTC[A/G]CTTCGTGCTTGCGCT | 11252 |
rs2018340 | snp | C/T | 0.451109 | 0.148509 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994313 | CCTCCCTATCTGACA[C/T]ATGGGGCTTGGGACC | 11252 |
rs2038058 | snp | C/G | 0.434687 | 0.168495 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938289 | GAGGATGAAAACACA[C/G]ACGGTTCTGAAGATC | 11252 |
rs2038059 | snp | G/T | 0.386694 | 0.20932 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938392 | AAACTGCATAAGGAA[G/T]CCTCCCCTCTGGAAC | 11252 |
rs2038060 | snp | A/G | 0.439502 | 0.163061 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944906 | AGTTCAAGACCAGCC[A/G]GGCCAACACAGTGAA | 11252 |
rs2038061 | snp | A/G | 0.371177 | 0.218669 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001855 | GTAAGCACTAAGGTC[A/G]GCTGGCCTGACCACT | 11252 |
rs2038062 | snp | A/G | 0.416055 | 0.186885 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001960 | GGAAAACAGGACACC[A/G]CTCAGTCTGAGAGTG | 11252 |
rs2038064 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913434 | cggtcagccaagatc[A/G]tgccattgcactcca | 11252 |
rs2056946 | snp | C/G | 0.377977 | 0.21476 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954371 | CACCAGCTATTAACA[C/G]TTAAAAAGTAGTTAG | 11252 |
rs2068943 | snp | C/T | 0.434687 | 0.168495 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960305 | CAGGATAATCTTACA[C/T]TGTCCCTACATGTGG | 11252 |
rs2068944 | snp | G/T | 0.427879 | 0.175668 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960436 | CTGGAGACAGGCAGG[G/T]GACCCCATGGTCTCT | 11252 |
rs2073199 | snp | A/G | 0.417683 | 0.185425 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879244 | CTGTCCTCAGTTCCT[A/G]CCCAGCGAGCCTGCA | 11252 |
rs2073200 | snp | A/T | 0.208779 | 0.246578 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872089 | TGTGGCTCTAATGTA[A/T]TAACGTGGTTCCATT | 11252 |
rs2076157 | snp | C/T | 0.434109 | 0.169127 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893230 | ACAAGGGCTATAGTC[C/T]TGTGTCCCCAAGGAA | 11252 |
rs2076158 | snp | C/T | 0.434109 | 0.169127 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893732 | GTCATGTTTACCACA[C/T]CCCTCTCCAAGAGTT | 11252 |
rs2077446 | snp | C/T | 0.439224 | 0.163383 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897678 | TAGGTACATGCTTGG[C/T]CCTCCGTCTGCCAGG | 11252 |
rs2092208 | snp | C/T | 0.445855 | 0.155373 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905303 | ACCTTTTCCTGTCTC[C/T]GCGTGTGCGATGCTC | 11252 |
rs2092209 | snp | C/G | 0.452719 | 0.146304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922642 | GGAGATTCTTCAGTG[C/G]TTGGGAAATAACGAT | 11252 |
rs2092210 | snp | A/G | 0.452719 | 0.146304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922694 | GCCCAAGGTGAGAGG[A/G]CCCTTTGATAAGGGA | 11252 |
rs2092211 | snp | G/T | 0.381113 | 0.21286 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922759 | GCACTCTTCTAAGCT[G/T]GGGGAGGGGCAGTGG | 11252 |
rs2092212 | snp | C/G | 0.453697 | 0.14494 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922942 | TGAGATAGAATGCGA[C/G]CTCTCTGAGGACTGC | 11252 |