| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs78399566 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903514 | ACTGCAATTTCCACA[A/T]CCTCATTTCTATGGG | 11252 |
| rs78430113 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957344 | TGAAGTGCTTTTGTT[C/T]CAGAAATTCTTCAAG | 11252 |
| rs78451882 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879966 | CACGAGTTCTCGGGT[A/G]GCGAACTGGCTTCAC | 11252 |
| rs78458538 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919687 | CTGAGGCAGGAGAAT[C/G]ACTTGAACCCGGGAA | 11252 |
| rs78536209 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930408 | GCTCTCAGACCTTCT[A/C]TGGACCCTCCTGTCC | 11252 |
| rs78615556 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943055 | CCATTTATTCAGGTC[C/T]TTTTAAATTTATTTC | 11252 |
| rs78621828 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905465 | CAGGCTCATTGGTGC[C/T]GCTGGCCCAGTGCCC | 11252 |
| rs78674790 | snp | A/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874322 | GAGACCGTGTCTCTA[A/T]TAAAAAAAAAAAAAA | 11252 |
| rs78692817 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990240 | ACTTGCAATCACAGA[C/T]GGCCACAAACCAACT | 11252 |
| rs78706664 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955487 | GGGGGAAAAAAAAAA[A/G]GGCTGTCAGGTGCTG | 11252 |
| rs78755475 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006087 | CATAAGCCACTGCAC[G/T]CAGCCACTCATGCCT | 11252 |
| rs78848567 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976462 | AGTCCACAGGATCAT[C/G]GATTTGAGGCAACAG | 11252 |
| rs78863249 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013378 | TTTGATGTAGTGGCC[C/T]CATATCTCAACCAGC | 11252 |
| rs78931907 | snp | A/C | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884006 | GCAAGACTCCGTCTC[A/C]AAAAAAAAAAAAGAA | 11252 |
| rs78937670 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008259 | AATTCAGTGGTCTTC[C/T]TTTTTTTTTGAGACA | 11252 |
| rs78967936 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977461 | AACACAAATTAAAAT[A/C]AAAGTGCTCCATAGA | 11252 |
| rs79018391 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909098 | ACAGGTCAGTATGGG[C/T]TCCTTCATTCGTCCA | 11252 |
| rs79032685 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931796 | TAACAACCAGGGTAT[A/G]TTCACTTACACAATC | 11252 |
| rs79053330 | snp | A/C | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894215 | TTTGTCAAGATCCTG[A/C]AGCCACAGTGGCTAG | 11252 |
| rs79064533 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909893 | CCGCAGGAACAGACA[A/T]TGACTGTGCACACCG | 11252 |
| rs79111274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959308 | AAATGGCAGCATGTA[A/G]TAAACATTAACGCCT | 11252 |
| rs79123390 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886305 | TAGGTGGATTGTAAT[A/G]TTTTAGCACTAAATG | 11252 |
| rs79192562 | snp | A/G | 0.0322114 | 0.122752 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872056 | GAAGGAGCCCCTGGC[A/G]CTGTTCTGGAATCTC | 11252 |
| rs79208428 | snp | G/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007237 | TTTTTTTTTTTTTTT[G/T]AGACAGTCTCGCTCT | 11252 |
| rs79221406 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935832 | ATCCCAGGGGCTCCA[C/T]GGCACCCCTGAGAGA | 11252 |
| rs79251637 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947834 | AGTGCCTGGAGTATG[A/G]GGACCTTCCACAAGC | 11252 |
| rs79264280 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912750 | AACTGAAGGACTCCC[A/G]TAAGCACAAACCACA | 11252 |
| rs79287700 | snp | C/T | 0.046775 | 0.145601 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952320 | AAATTTATTTATTTA[C/T]TTATTATTTTATTTT | 11252 |
| rs79313729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924571 | CTCACCTCCACCGAG[C/G]TACTTTGTCCTCAGA | 11252 |
| rs79337714 | snp | C/G/T | 0.0392288 | 0.134937 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870804 | GGCTAAGCCTACACA[C/G/T]GGCGTGGCTGAGTAA | 11252 |
| rs79358373 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933888 | GTATGAACAAGCAGA[C/T]GAGGAAATATTATGG | 11252 |
| rs79395722 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901240 | TCCTGGCGTACCCCT[C/T]GCCAGGCAAGCCCAT | 11252 |
| rs79437311 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984826 | CTCAGCACATCAACA[A/C]CCAGCTTAGTAACAA | 11252 |
| rs79499990 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993733 | AGGCCGACCAGAGCC[A/G]AAGGACACTCTCCGG | 11252 |
| rs79521923 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918741 | AGAGTCCCACCACCT[A/G]CCAGGGAGGCTGGAG | 11252 |
| rs79551363 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926399 | AACAGCCAGCATCTC[A/C]AGGCAGACACAACTC | 11252 |
| rs79596583 | in-del | -/CCAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913479 | AGCGAAACTCCGTCT[-/CCAAA]AAAAAAAAAAAAAAA | 11252 |
| rs79642048 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921740 | AACTTCATTTAGAAG[C/T]TTTTTTTTTTTTTTA | 11252 |
| rs79661757 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942663 | CACTTGTTGAAAAGA[C/T]TTTTCTTTCCCCCAT | 11252 |
| rs79712511 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960500 | CTCAAATACGCAACT[C/G]TGATTACATGGAAAT | 11252 |
| rs79721418 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955414 | GAAATAAGCCCAGAG[C/T]TCACTCAGGTGCCTG | 11252 |
| rs79729676 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999675 | CTCCATCTCAAAAAA[A/C]AAAATGCTGTCTACA | 11252 |
| rs79741935 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991814 | GGCTATCCACAGACA[A/C]AAAAAAAAAAAAAAA | 11252 |
| rs79769049 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918174 | CACACCAGGGCCACT[A/G]CAGACAGGCCACACC | 11252 |
| rs79793953 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928225 | TGGCCCAAAGAAACA[A/C]CTTGGCTAAAAAATG | 11252 |
| rs79852374 | snp | C/T | 0.030665 | 0.119967 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878908 | AACCTCCCAGGTGTC[C/T]AGGCTGGGCCACGGC | 11252 |
| rs79883834 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983416 | GATCACTTGAACCCA[A/G]AAGGCGGAGGTTGCA | 11252 |
| rs79940798 | snp | G/T | 0.0685586 | 0.173535 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934177 | GTTTTAGAGTTGAGA[G/T]GGGAGTATGGAAACG | 11252 |
| rs79968294 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963649 | TGTTTTACAGGGAAG[A/G]AAACCACCACAGAAC | 11252 |
| rs80081809 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932952 | TCTGAATCAGAGGAA[C/T]CAACTGTGTTAGGAG | 11252 |
| rs80083031 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007903 | ATGCTCCCTCCACAT[A/G]AGCCACTGAGATATC | 11252 |
| rs80095186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944644 | GCAAAAATTGGAAAC[A/G]AGTCAGCTGCTCAAA | 11252 |
| rs80099429 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982891 | AAAAAAAAAAAAAAA[A/C]AACAACAAGGCTAGG | 11252 |
| rs80131464 | snp | C/G/T | 0.0558544 | 0.157504 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974845 | AGAGGAGGAGGAGGA[C/G/T]GAGGAGAAGGAACAA | 11252 |
| rs80136666 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906505 | GGCAGCCCACACGTC[A/G]AGGGCCCTGATCTGC | 11252 |
| rs80140090 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884288 | AGACCTCCTGATGAA[C/T]GCGCCATCCCAAACC | 11252 |
| rs80149927 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999002 | CACCTCCATCACTCA[A/G]TAAAATCCCGCATTC | 11252 |
| rs80155340 | snp | A/G | 0.00601529 | 0.0545111 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891231 | CGCCGGCCATGGTGG[A/G]GTCTGCTCTGCTCAC | 11252 |
| rs80161379 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969072 | CCATCCATCCATCCA[C/G]CCTATTGGCTCTGAC | 11252 |
| rs80189793 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922413 | CAAGAACATTCTGAG[A/T]AAAAAGACCATGTTG | 11252 |
| rs80259910 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954483 | TCATTGCAGCCTCAA[C/T]CTCCTGGGTGTAAGC | 11252 |
| rs80273835 | snp | C/G | 0.0387552 | 0.1337 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872305 | AGCTCAGAGCCCAGG[C/G]GTGGGCAGGGGCCTG | 11252 |
| rs80286931 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893187 | AGTTCTGAGTTAACT[C/T]GGCAAGTGCAAGTGT | 11252 |
| rs80321704 | snp | G/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952680 | TTATTTTTTTTTTTT[G/T]GAGATGGAGTCTCGC | 11252 |
| rs80337814 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874852 | GGCATTGGGCATCCG[C/T]TTTTTTTTTTTTTTT | 11252 |
| rs111228786 | snp | C/T | 0.130694 | 0.219696 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894530 | ACAGGCGTGAGGCAC[C/T]GCGCCCAGCCCAAAG | 11252 |
| rs111251931 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869962 | TCTGCTCACTGGAAA[C/T]GGAGTGAATGCATAG | 11252 |
| rs111253484 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898514 | GAACTCAGGTGATCT[A/G]CCCACCTCAGCCTCC | 11252 |
| rs111256326 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911552 | ATGGGTACAGACTGG[C/T]GGCAGATGCTCCAGC | 11252 |
| rs111257590 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960962 | AAATATTTCAAGGGA[C/T]CAATTTCTGCTAGGT | 11252 |
| rs111276727 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005571 | ACACCAATGACCTGC[A/G]ACTACACCCGTGACC | 11252 |
| rs111337792 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934503 | CCTGGGGCCTCCCCA[C/T]TCTGGCTTCCCAGCC | 11252 |
| rs111348564 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962005 | CACAGAAGATGAACA[A/C]CAGAGTGCCACGCCC | 11252 |
| rs111358069 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999593 | GAATCGCTTGAACCC[A/G]GGACGCGGAGGTTGC | 11252 |
| rs111359451 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013576 | TCTTGGGCAAGAACA[A/G]GAGGGCTGGCATTCA | 11252 |
| rs111437031 | snp | C/G/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892580 | TGACGACACTGCCAC[C/G/T]GACCAAGGGAGCTGA | 11252 |
| rs111453195 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012740 | TCACCGCAACCTCCG[C/T]CTCCTGGGTTCAAGC | 11252 |
| rs111516988 | in-del | -/TAT/TATTTTT/TATTTTTT | 0.32955 | 0.237006 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010398 | ACATATATATATATA[-/TAT/TATTTTT/TATTTTTT]TTTTTTTTTAATTGA | 11252 |
| rs111545358 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983253 | ATCCAGGAGGTGGAG[C/G]CTGCAGTGAGTCGAC | 11252 |
| rs111580230 | snp | A/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968575 | CACCTAGGAAAACCT[A/T]GAAACCTAGTAAAGC | 11252 |
| rs111595676 | in-del | -/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972062 | GCGGTTTTGTCCAAT[-/G]GGGGGGGGGAAATGT | 11252 |
| rs111620194 | snp | C/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887223 | AGGGGTTTCCCAGAG[C/G]ATTCTGACACTTGGT | 11252 |
| rs111621080 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965057 | AGGACATCAAAACCC[-/A]ACTGTGTGTGGCATC | 11252 |
| rs111628648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938638 | CAGGACCATTTAGGT[C/T]GCACCATCTCCCTCT | 11252 |
| rs111638389 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920866 | GAAGTGCAGTGGTGT[C/G]ATCACAGCTCACTGC | 11252 |
| rs111670760 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972115 | ATTGTTACTGTGTCT[A/G]TGTGGAAAGAAGTAG | 11252 |
| rs111678739 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871861 | CCCCAGGGCCCCGGC[C/T]GCCTTGCTCCCAGCA | 11252 |
| rs111691849 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921448 | AACCCACCTGGGGCA[C/T]TGCCCAGACTCTTAC | 11252 |
| rs111701176 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926844 | GAGACCCTATCTCTT[-/A]AAAAAAAAAAAAATG | 11252 |
| rs111741346 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012240 | CAAGGTGGCAGGCGC[C/T]TGTAATCCCAACTAC | 11252 |
| rs111762910 | snp | A/C/T | 0.0566069 | 0.158427 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012713 | GCTGGAGTGCAACGG[A/C/T]CGGATCTTGGCTCAC | 11252 |
| rs111784829 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986981 | TCACACATACCTACA[C/T]GCACACATACATAGA | 11252 |
| rs111792107 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938419 | GAACACACAGGAGGC[A/G]TCAGAAAGAAGCCTG | 11252 |
| rs111795540 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987953 | CAAGACCAGCCTGGC[A/C]AACATGGTGAAACCC | 11252 |
| rs111852095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970458 | TACTGCATCAATGTT[A/G]ATTTCTTAATTTCAA | 11252 |
| rs111863522 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902877 | CCTCAGCCTCCCAAA[C/G/T]TGTTGGGAATACAGG | 11252 |
| rs111865712 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889977 | GAATAAAGAAAGGCT[A/C]CTGCACACGCAGAGC | 11252 |
| rs111869015 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943124 | TTCTCTTCATAAATT[C/T]ACTCCTATTTTATTC | 11252 |
| rs111941175 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971811 | GGAGGTGGGGGGCAG[A/C]CCCCGCCCGGCCAGC | 11252 |
| rs111943819 | snp | G/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881538 | TGCTTAAGCCTCAGG[G/T]GCACCAGGACCTTTG | 11252 |
| rs111945531 | in-del | -/ATGCTAAAGAGT | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907232 | GCTCGTGTCTTGGCC[-/ATGCTAAAGAGT]ATGCTTCTATTTTGA | 11252 |
| rs111948232 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890593 | TGTGGTGGCATGTGC[C/T]GGTAGTCCCAGCTAC | 11252 |
| rs111997643 | snp | C/T | 0.0444908 | 0.142359 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015982 | GGTCAGCCCAACCCT[C/T]GAGAATAATAATGAT | 11252 |
| rs112001207 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902080 | CACTGTGTGTGAAGG[A/G]CCACGAGGCCCTAGG | 11252 |
| rs112048118 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971798 | CCCCATCCGGGAGGG[A/G]GGTGGGGGGCAGCCC | 11252 |
| rs112049144 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990467 | AGAAGACAAACAGGT[C/T]GGTCATACCATACAT | 11252 |
| rs112051070 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945712 | CCCACTTGGCTCTGT[C/T]CCCATGATGATAGCT | 11252 |
| rs112054494 | snp | A/C | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871824 | TGTGCCCCTCCCTCA[A/C]GTTGGGCCTCTTCTG | 11252 |
| rs112095367 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912160 | TCTGTAGACAAACCT[A/C]TAAATGAAAAACATA | 11252 |
| rs112103667 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891549 | GGGATTACAGGTGCC[C/T]GCCACCACGCCTGGC | 11252 |
| rs112149965 | snp | C/T | 0.084364 | 0.187256 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993111 | CCCGGGAGGCGGAGG[C/T]TGCAGTGAGTCGAGA | 11252 |
| rs112197656 | snp | A/C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892621 | GCCCCTCCTCTGCCA[A/C/T]GTGCCTGCTCCACAG | 11252 |
| rs112197938 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921374 | AAAAAAGAAAAAAGA[A/G]AAAAAAAAAAAAAGC | 11252 |
| rs112198948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918214 | CCATGCTCAACCTCA[C/T]AGGGAGTCCAAGGAG | 11252 |
| rs112203435 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946477 | CAAGAATCACTTGAA[C/T]CCAGGTGATGGAGGT | 11252 |
| rs112212597 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877865 | CCTCAGGGCACAGGC[C/T]CCCAAAGCACTGGAT | 11252 |
| rs112239995 | in-del | -/AGGCCCC | 0.120326 | 0.21374 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957103 | CCCCACTTCTTCTCT[-/AGGCCCC]AGGATAATGTCGCCT | 11252 |
| rs112266514 | in-del | -/A | 0.119281 | 0.213102 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952668 | GGCCTATTTATTTAT[-/A]TTTTTTTTTTTTGAG | 11252 |
| rs112285082 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923250 | CAATGCATGATATAT[G/T]TAACAATCCGACTTC | 11252 |
| rs112288599 | snp | C/T | 0.11963 | 0.213316 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952632 | AAAGTGCTGGGATTA[C/T]AGACGTTGAGCCACC | 11252 |
| rs112307551 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925349 | GCTGTGTGTGGTGGC[A/G]CATGCCTGTAGTTCC | 11252 |
| rs112309081 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984601 | ACACCTGCTGCAAAG[G/T]TTCCTGGTGCAAAAA | 11252 |
| rs112313612 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948472 | ATGTGCCTTTGAAGT[A/T]TAAAAAGCCACACGA | 11252 |
| rs112316084 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874926 | CGCAATCTCGGCTCA[C/T]TGCAAGCTCCGCCTC | 11252 |
| rs112331742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874597 | TGGGGTCTGGGCAAA[C/G]CTGTGGCTCTCCTGA | 11252 |
| rs112345080 | in-del | -/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890015 | GGACTTTTTTTTTTT[-/G]TTTTTGAGACAGAGT | 11252 |
| rs112389510 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914097 | AACCAGGCTCTCATG[C/G]AGAGAACTCCAGTGA | 11252 |
| rs112404789 | snp | C/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985741 | CATTATATTCAGAGG[C/G]AGGGCTAAGGTCTGA | 11252 |
| rs112471327 | snp | A/C | 0.444444 | 0.157135 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900718 | GGCTCAAGCAATCCT[A/C]CCAACTTGGACTCCC | 11252 |
| rs112471921 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003673 | TATGTGATATCACAA[A/C]GTTGACAAAATGTGA | 11252 |
| rs112484924 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915409 | AAAGGCCCATACTTA[C/T]TCACTTTCCTTCTGT | 11252 |
| rs112492672 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969846 | AGGGTGAGGCTGCAA[A/T]GAATCATGATCCCAC | 11252 |
| rs112494209 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926292 | TCACACTGAGGCCTA[C/G]AGCTCAGCAGGTCCT | 11252 |
| rs112498162 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952592 | TCAGTCTCCTGACCT[C/T]GTGATCCGCCCACCT | 11252 |
| rs112508356 | in-del | -/T/TTTT | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874853 | GCATTGGGCATCCGC[-/T/TTTT]TTTTTTTTTTTTTTT | 11252 |
| rs112527272 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878936 | GGCCCACAGAGCTCA[A/G]GAGCCCAGGAACCTC | 11252 |
| rs112569068 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902716 | CCTCCTGGGTTCAAG[A/C]GATTCTCCTGCCTCA | 11252 |
| rs112573018 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890236 | CAATCTCCTGACCTC[A/G]TGATCCGCCTGCCTC | 11252 |
| rs112577247 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929089 | TGCAGTGAGCATGGC[C/T]GCAAAGATCCTCCCT | 11252 |
| rs112579495 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943244 | TATTGATCTTATATC[C/T]TACAACCTTGCTGAA | 11252 |
| rs112581341 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903091 | CTGCAGGGCCTCACC[A/G]GGCCTTCACTGCAGC | 11252 |
| rs112592077 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955477 | GATAGCATCAGGGGG[-/A]AAAAAAAAAAGGCTG | 11252 |
| rs112651007 | snp | A/G | 0.0123403 | 0.0775749 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006356 | ATTTGGCCAAAAGCC[A/G]CACAGTCACCTAGTG | 11252 |
| rs112656806 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917661 | ACACGCACTGCTCTG[C/T]GGTGTGCCGTGATGA | 11252 |
| rs112659263 | snp | C/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910437 | CGCTCCTGCACTAAT[C/G]AGGCCACAGCCTCTC | 11252 |
| rs112660561 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921962 | CAGGCTGGTCTCGAA[C/G]TCCTGAACTCAGGTG | 11252 |
| rs112675206 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951340 | CACCCTGTGCACACC[C/T]GTGGTGCCCAGGGCT | 11252 |
| rs112677028 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987758 | CCAGGATGGTCTCAA[C/T]CTCCTGACCTCATCA | 11252 |
| rs112710631 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42981820 | CCCAGTCCGGGAGGG[A/G]GGTGGGGGGTCAGCC | 11252 |
| rs112729941 | snp | C/G/T | 0.00329009 | 0.0404255 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876976 | TGGACTGTGACTGCG[C/G/T]AGACTGGGCGGGGTT | 11252 |
| rs112736159 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955050 | CCACTCCCTCTAAAA[C/T]TCATCATCAAACTGG | 11252 |
| rs112746996 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005496 | GGGGAGAAAGACAGG[C/T]CCTGTAAGTGCCAGG | 11252 |
| rs112748763 | snp | C/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899554 | AAGGCCAAGTGTGGG[C/G]AGAGGTGGGTGTACA | 11252 |
| rs112750968 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905249 | GGGGGGAAGACAGGT[C/T]TGTCTGCACAACAGA | 11252 |
| rs112770364 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989215 | AGAAAACTCAATTCT[C/T]GGCCGGGCGCAGTGG | 11252 |
| rs112806846 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983137 | GCCTGGCCAACATGG[C/T]AAAACCCCGTCTCTA | 11252 |
| rs112807995 | in-del | -/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924759 | GTGAGGTTTTTTTTC[-/T]TTTTTTTTTTTTTTC | 11252 |
| rs112822056 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991919 | TATAACATTTCTAGA[C/T]GAGACATGAGAAAAC | 11252 |
| rs112830718 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893138 | AACTAAGGTGCCAAG[C/T]GGCAAGGCCTTCCAC | 11252 |
| rs112831223 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998894 | TTGAGCTGGGGGCAG[C/T]TGAAGAGGAGATCGG | 11252 |
| rs112843745 | in-del | -/AGG | 0.0456336 | 0.143994 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988232 | CAGGCACCAAAGACA[-/AGG]AGAAGATAGTCTCTG | 11252 |
| rs112848425 | in-del | -/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878331 | CTGGGGAGCCTGGGT[-/G]GGGGCTTCAGTGCCT | 11252 |
| rs112849281 | snp | C/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891903 | CAGCCCTGCTTGGCC[C/G]CTGGCTAGCCCTGCA | 11252 |
| rs112851908 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956782 | TAACCCCTTCTCAGT[A/T]TGGAGCAATGCCAGC | 11252 |
| rs112857000 | snp | A/C | | | splice-acceptor-variant, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912158 | AATCTGTAGACAAAC[A/C]TATAAATGAAAAACA | 11252 |
| rs112865886 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939498 | TAGAGCAGGCCTAAC[C/T]GAACCAGAACGATGC | 11252 |
| rs112868156 | snp | A/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972138 | AGAAGTAGACATAGG[A/T]GACTCCATTTTGTTC | 11252 |
| rs112931214 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924858 | GCCTCCCGGGTACAC[A/G]CCATTCTCCTGCCTC | 11252 |
| rs112962498 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906567 | AATGGAAATGTCCAC[G/T]ATAGCTCAGGGGGAG | 11252 |
| rs112997888 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978416 | AAATCTAACAGAAAA[A/T]ATCAGTCTTCGTTTA | 11252 |
| rs113005387 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871775 | CTGTGCCTTCCTCAC[C/T]ACCCTGGCCAGGTGG | 11252 |
| rs113016072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895250 | GGAAGTGACATTATG[C/T]GGTTGCTTCCCTTAA | 11252 |
| rs113020492 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917272 | ACTGATCTTAACCAC[C/T]TCAGTGCTGAGTTCA | 11252 |
| rs113057498 | in-del | -/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898278 | ACCTCCTTCCTTTTC[-/T]TTTTTTTTTTTTGAG | 11252 |
| rs113096102 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889141 | TAGGGGAGGACAACT[A/G]AGACGGAGCATGGGG | 11252 |
| rs113108334 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884664 | ATTCCAAATGCAAAG[-/A]AAAAAACAGGAGCTC | 11252 |
| rs113108730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949129 | GGGATCCTGTCTCTA[C/T]AAGGACAAAACATTT | 11252 |
| rs113144965 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004995 | GTAAAATGCAAATGC[C/T]TAGACAACCAAGCTC | 11252 |
| rs113150084 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971547 | CTGCCTGGCAGCCCA[C/T]CGTCTGGGATGTGAG | 11252 |
| rs113153408 | snp | A/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009869 | TTATTTTTTCTATTT[A/T]TTTTTTTTTTTTTTT | 11252 |
| rs113167068 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009058 | AAAACAGTCCTTTCC[A/G]GCAGATGAACAAATA | 11252 |
| rs113192315 | snp | A/C | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902147 | TCATGGAACTTATGG[A/C]CAGAAAAATAATGCA | 11252 |
| rs113204799 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983448 | TGAGCCGAGATTGTG[-/C]CACTGCACTCCAGCC | 11252 |
| rs113227841 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911368 | TGAGCCATGATGGTG[C/G]CACTGAACTCCAGCC | 11252 |
| rs113280315 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932786 | AAGCCAATTCTTCCA[C/T]AATGGCCAGCTTGTA | 11252 |
| rs113280506 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897084 | TGGAACTACAGGTAC[A/G]CACCACCACACCTGG | 11252 |
| rs113281286 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964789 | ATTAGGAATTTGTAA[C/T]TCCCCATCTCCAGAA | 11252 |
| rs113339314 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870396 | CAAGCAGTTTACAAA[C/T]GAAACTCACTGTTAA | 11252 |
| rs113343471 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989901 | ACACACACACACACA[C/T]ATATGTATATATATG | 11252 |
| rs113372886 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954241 | GCACTCCAGCCTAGG[C/T]GACTGGGCAAGACCC | 11252 |
| rs113405676 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908373 | CCCAGAGCCTACTGA[A/C]TGAAGGTAAGGGAGG | 11252 |
| rs113430488 | in-del | -/C | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884249 | CAGATTACAAAGAAG[-/C]AGGAGGCCCTGAGGG | 11252 |
| rs113457423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996314 | CAAGATGGGTGGATC[A/G]CAAGGTCAGGAATTC | 11252 |
| rs113459245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001213 | TGGGAAGCTCCAAAC[A/G]ACAAAGGGGAGCTAA | 11252 |
| rs113490524 | snp | A/T | 0.0479149 | 0.147179 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896616 | TGGTCTTTTGTGGGG[A/T]CATAAGCTTCCATGA | 11252 |
| rs113491959 | snp | A/G/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902551 | AGGGACTGAGAAGTC[A/G/T]CTGAGATCTCAGAGG | 11252 |
| rs113518550 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880554 | GCACACCCACCCATG[A/C/T]GGGCCACAGACACCC | 11252 |
| rs113522813 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929076 | AAGAGTGTGTATGTG[C/T]AGTGAGCATGGCTGC | 11252 |
| rs113540256 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890137 | CTCCTGAGTAGCTGG[A/G]ACTACAGGTGCCCGC | 11252 |
| rs113549329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909025 | GGAGGTACTCCTTCC[A/G]AATATGCATTAAATA | 11252 |
| rs113550627 | snp | A/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917304 | ATCTTCTAGAACATA[A/T]AACATGAAAAACTAA | 11252 |
| rs113550941 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966199 | AAATGGTGAAACCCC[A/G]TCTCTTTGAAAAATA | 11252 |
| rs113606884 | snp | A/G | 0.000149252 | 0.00863736 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876850 | GAAGAGAGACAGAGT[A/G]AGCGCGGTGGGAGCA | 11252 |
| rs113608261 | snp | A/C | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884923 | ATCTGGCCCACAGCA[A/C]AGGTGGGGCTGGGGC | 11252 |
| rs113630394 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884005 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 11252 |
| rs113641284 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969711 | TGAGAGGCCGAGGCA[C/T]GATGATCGCTCGAGT | 11252 |
| rs113671089 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901514 | GGCCCTGCCCCAAAA[C/T]GTGTAACTTTGTACA | 11252 |
| rs113673150 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958243 | TGACCTTGGACAAGT[C/T]GTCACCTCTGGATCC | 11252 |
| rs113691073 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982145 | GACAGCCCCCCGCCC[C/G]GCCAGCCGCCCTATC | 11252 |
| rs113739519 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986173 | GGAAGACCAGGAACT[A/G]TGCTAGGAGATTTAA | 11252 |
| rs113790119 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890721 | CTTTGTCTCAAAAAA[C/T]AAAAATAAAAAATTT | 11252 |
| rs113790468 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899179 | TTCCACAGGGTCTAC[C/T]GCACAGCAGGCACCC | 11252 |
| rs113791360 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943871 | TTGCACAATACAATA[C/T]AGAAAGCAAAGAAAG | 11252 |
| rs113816756 | in-del | -/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914241 | CACCTCTCACAGTAA[-/T]TTTTTTTTTTAGGTG | 11252 |
| rs113816881 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876449 | GCTGAGGGCTCCTTC[C/T]GAAGGAGCACAGGTG | 11252 |
| rs113817918 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922534 | TCGCTGCCACGGCCC[A/G]AGCACACCTGGCTGG | 11252 |
| rs113819904 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987271 | AACAGCACTAACCTT[C/G]GGTACCCCAACACTG | 11252 |
| rs113822836 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992652 | GTTAATAGCACCTTA[-/C]TTTTTCTGTAACATC | 11252 |
| rs113823565 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887321 | CAGTGGAGAAAGGGC[A/G]TATGTATGGGCTTGA | 11252 |
| rs113850279 | snp | C/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911360 | GGCTTCAGTGAGCCA[C/T]GATGGTGCCACTGAA | 11252 |
| rs113903676 | snp | A/C/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43015018 | ACCTCGGCGGCCACT[A/C/G]ACCTCCCAATCCGTC | 11252 |
| rs113912148 | snp | A/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881302 | TCCCTAACAGCCCCC[A/G]ACAGGAGATGGGTGC | 11252 |
| rs113913432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890280 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 11252 |
| rs113997651 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899241 | CCAGAAGAAAATGAA[C/T]GCGAATACCTTTGTG | 11252 |
| rs113998647 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916382 | CTCATTTCTGATGTT[A/C]ACAGAGCAACAACCT | 11252 |
| rs114022410 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902582 | CATGGTCAACCAAAC[A/T]ACTCATGATCCTTTA | 11252 |
| rs114048169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992333 | TGCGCGCAAAGCACT[C/T]TGGAAAAGTTTGGCA | 11252 |
| rs114084454 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969647 | GTTTCTACGTAGAAA[C/G]TAGAAACTAGGTCAG | 11252 |
| rs114092566 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871057 | ACCCACCATTGACTC[A/G]GAAAGGAGAGACAAA | 11252 |
| rs114105731 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890793 | AATGTCAACTACCAT[A/G]GGCTTCTAGCCTGAG | 11252 |
| rs114106081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013689 | GGAATAACCGCAGAG[A/G]AAGGCACCGAAAAGG | 11252 |
| rs114124646 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952295 | TATCTTAATGACTCT[C/G]CTGTTGAAGAAATTT | 11252 |
| rs114138895 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883351 | CAGCGGTGCAGTAAC[C/T]GTTGCTTTTGATGAT | 11252 |
| rs114176728 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922507 | TGCAGAGGTAGGCAG[A/T]GGTGGACATCCTCGC | 11252 |
| rs114183010 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964645 | ACAGGGCAGGCTCTA[C/T]AGTTCCTATGTACCT | 11252 |
| rs114184817 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948236 | AGAGGGGACTGACAA[A/C/T]TGGCAGGGCGCTGAA | 11252 |
| rs114215350 | snp | A/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997177 | TGACCAGAATGTAAG[A/T]TCATGGACTACGTTG | 11252 |
| rs114235029 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955776 | AGGTGACCGTCCCTA[C/T]AGATGGGAAAGTAGT | 11252 |
| rs114244130 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962468 | AACACTGCCCCTCCA[A/G]CTTGACTTCCCTCAA | 11252 |
| rs114312370 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966066 | ATATGTTTCATGAAC[C/T]AAGATGTAAATAGAG | 11252 |
| rs114362032 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998054 | CCAGCCCCAAACATA[G/T]CCAAGGGCAGTTACC | 11252 |
| rs114363819 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976355 | AGGCCACTGGCAAGC[A/G]CAGGCCTTAATGCAC | 11252 |
| rs114371061 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986957 | TGAGTAAAGTTTATT[A/G]GATGTAAATCACACA | 11252 |
| rs114385074 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965855 | TATGATAATTTAAGG[C/T]ATTAGTTTCTCTCTT | 11252 |
| rs114399722 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998638 | TAATCATAATCACAG[C/T]ATCATTTATATATAG | 11252 |
| rs114563499 | snp | G/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900952 | TTCCAGCCAGCCCTG[G/T]GGGCGCCAGCAAGTC | 11252 |
| rs114573599 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918084 | GATGTGAAAATGCTT[C/T]GTAAAGTAAAAATGT | 11252 |
| rs114581013 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927323 | CGATCTTAGCTAACT[A/G]CAACCTCTGCCCCCG | 11252 |
| rs114635290 | snp | A/G | 0.4628 | 0.13121 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916420 | GGGTGGGGATGGGGG[A/G]TGGGGAAGGGGGGCC | 11252 |
| rs114652987 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947281 | CTTCGAGGTCTGCTG[C/T]GCCAGGTTCCCAAGA | 11252 |
| rs114670155 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016377 | GAACCGGCTAGGCAC[A/G]GTGGCTCACGCCTGG | 11252 |
| rs114693902 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895798 | GAGCACAGAGCCAAC[A/G]GGAGAAGGGCAGTAT | 11252 |
| rs114817520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887836 | GGGGCAGAAAATCTC[C/T]GCTTCACAACAGAAA | 11252 |
| rs114861145 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898962 | ATCCAAAGAGGCCAC[A/G]TCAGCTCCTCCTCCA | 11252 |
| rs114890139 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984208 | AACTCCCAAACTCAA[C/G]TAATCTGCCTGTCCC | 11252 |
| rs114893618 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932181 | AGGATCTTCTCTCTG[A/T]TTCTTCAACATAATA | 11252 |
| rs114970386 | snp | G/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908055 | ATTCCCAGAATATTT[G/T]ACACAAGATACTTAT | 11252 |
| rs114978663 | snp | A/G | 0.031825 | 0.122064 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872396 | CGTCAGGAGCAAGCA[A/G]TTGGTGGGAAAGAAA | 11252 |
| rs114980185 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874072 | TGGGATTACAGGTGT[G/T]AGCCATCGTGCCCGG | 11252 |
| rs114982822 | snp | C/G | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885248 | CACATTCATCTGGTG[C/G]GGATGTGCCTCGAGG | 11252 |
| rs114985150 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878631 | ACTGGCGCCTGCACA[A/C]AATACAGAGTGAGCA | 11252 |
| rs115020390 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42995205 | TGACTGCAGAGAAAC[G/T]GCACCCTGGCATTCA | 11252 |
| rs115023343 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883339 | GTGGCAGAGCAGCAG[C/T]GGTGCAGTAACTGTT | 11252 |
| rs115089835 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925870 | CAGCTGCGGCCCATG[A/G]GTCCCTGGGCCCTCT | 11252 |
| rs115151065 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934573 | CCACACGTGCAGCAC[A/G]CTGCCACCTGAGACT | 11252 |
| rs115160501 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001989 | TGAATACCTAAGGGA[C/T]AGTGGAGGGTAGGAA | 11252 |
| rs115162568 | snp | C/G/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965675 | ATCCTCTACCAATGA[C/G/T]TTTGGTAGAGGATCC | 11252 |
| rs115193994 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922566 | TGGGTTCTGGCCGCT[C/T]CACAGGCCTTGCACT | 11252 |
| rs115204312 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992147 | AAATATATTTTAAAA[A/G]TTTCAAAACTAAGTT | 11252 |
| rs115207174 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886079 | ACACAATAGCCTCCC[A/G]GGAGCTCTCAGGGTA | 11252 |
| rs115219794 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953067 | TAAATATATTGGATA[A/T]ATCTAAATAGCATTA | 11252 |
| rs115301482 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935368 | ATGGGGCGGGGTGGG[A/G]GGAAGAAGGCTCTCC | 11252 |
| rs115344284 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930432 | CCTGTCCTCGTGTCT[C/T]ACGCAGAGCCTAGCA | 11252 |
| rs115351044 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893816 | AAGATCATACACATC[A/G]GTGAACGGGGGCTTC | 11252 |
| rs115387484 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950643 | TACAGTAACATTCAA[C/T]GCCATAAGTAGCATT | 11252 |
| rs115392773 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959008 | TCAGTTATTAAAACA[A/G]TAAGACTTTTACATT | 11252 |
| rs115518889 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935839 | GGGCTCCATGGCACC[C/G]CTGAGAGATGACCTA | 11252 |
| rs115541936 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882465 | TCAGGTGGAAGGTCA[C/T]GGGCCGCCACGTGCA | 11252 |
| rs115546275 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962494 | CTCAACGGTCAGAAC[C/T]GGGTCTTGGATAGTT | 11252 |
| rs115558763 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877621 | AGGGAAAATCCAGTC[A/G]TGCAACTGCCTACTG | 11252 |
| rs115595172 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977611 | GGGTTGATATGGTTA[C/G]GCTCTGTGTCCTCAC | 11252 |
| rs115603388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967370 | AGCCAACACAAGGCC[A/G]CCAACTTTATTTTGC | 11252 |
| rs115607093 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906632 | AACTATTTTCTCACT[A/G]GCTTAGAAGGAATTC | 11252 |
| rs115626436 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929902 | CCAAATGTCAGCTCT[A/G]CTGCCTGGCCTGCCT | 11252 |
| rs115656758 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985664 | AACAGACACACACAC[A/G]GACACATTCACATGT | 11252 |
| rs115659490 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964129 | TGTGTTTTACAAGGT[A/G]ATTCTTGGCTGGGCA | 11252 |
| rs115733401 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921246 | CGCCTGTAGTTCTAG[C/T]TGCTCGGGAGGCTGA | 11252 |
| rs115777278 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962446 | CAGCCTGTAAGCCAG[C/G]CTACACAACACTGCC | 11252 |
| rs115830011 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970941 | GCTCCCTGCACCACC[C/T]TGCCCTGCCCCCAGC | 11252 |
| rs115841379 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951002 | TCTACCTGGACATAT[C/G]GTGGTCAGGGAAGGT | 11252 |
| rs115851629 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939070 | AAGGTAGGACAGGCC[C/T]CAAGGTCACCCGTCC | 11252 |
| rs115857270 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872026 | GCCATGTGTCAACCC[C/T]TCCTGAGACCCTGAG | 11252 |
| rs115859503 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950425 | AGGGAGGGAAGGGAG[A/T]GGGCAGGTGGGCAGG | 11252 |
| rs115896675 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953325 | GCAATGGAAAATGGG[C/T]ATGATGAAATGCAAT | 11252 |
| rs115903478 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992902 | GAAGTGGTGGCTCAC[A/T]CCTGTAATCCTAGCA | 11252 |
| rs115904342 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959159 | GGAGGGGTCCTGGAG[C/T]GGTGGCAGGTGATCA | 11252 |
| rs115963142 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896996 | GGCTAGAGTGCAGTG[C/T]CACAATCATGGCTCA | 11252 |
| rs115996988 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010924 | GTCAAAACTTGTGCT[A/C]TTTGGTGGCCACTGT | 11252 |
| rs116027166 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881877 | GAGGTCCTGTGTGCC[C/T]ACGGCTCCTGAGACT | 11252 |
| rs116068201 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991026 | TACACAAAGTGCTTA[A/C]AGCAGAAGAAAGCTC | 11252 |
| rs116068701 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994434 | ACAAAGACCCTCGGG[C/T]GTGCTTATGGGGACA | 11252 |
| rs116071422 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950644 | ACAGTAACATTCAAC[A/G]CCATAAGTAGCATTC | 11252 |
| rs116236003 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966403 | TTACTCATCCAACAC[A/G]TGTACATAAAAAGGA | 11252 |
| rs116243943 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934486 | CTGCACACAGAACAC[C/G]TCCTGGGGCCTCCCC | 11252 |
| rs116264698 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977417 | AGAAAAAAGGTGAAA[C/T]GGTGCTCAACCTCAC | 11252 |
| rs116270722 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913064 | AGCCTGGAATTGGAG[C/T]AAGAAACACAGACTC | 11252 |
| rs116275088 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907756 | TGGCTCTAGGAGGCC[A/C]GAGGCTGGGCTCTCA | 11252 |
| rs116296560 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993078 | GCTGGGAGCTGGGAA[A/G]CAGGAGAATCACTTC | 11252 |
| rs116309630 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901571 | TTCAGTTGTCAGGTA[A/G]AGTCAGAGCTATTCC | 11252 |
| rs116318580 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013083 | AGGCGTGAGCCACCC[C/T]GCCCAGCCTAGATTA | 11252 |
| rs116352227 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985321 | GCTTTGGCGACAGAG[C/T]GAGACTCCATCAGCT | 11252 |
| rs116353247 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951233 | ACGAGCCTTATCTTC[C/T]AGTCACGATAACCGG | 11252 |
| rs116354362 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921003 | GTTTCGTCGTATTGC[C/T]CAAGCTGGTCTTGAA | 11252 |
| rs116360103 | snp | A/G | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947483 | TGCTTGGAGGCAGCC[A/G]TTTCAGAGGCTCTTC | 11252 |
| rs116380558 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994652 | TCCCTGTGCATGGCC[C/T]AAAGGGAGAGGCACA | 11252 |
| rs116385458 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924802 | AGCTCTGTCGCCCAG[A/G]CTGAAGCGCAGTGGC | 11252 |
| rs116435257 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992759 | CAAATTGTAGCATGC[A/C]CATGCATTGGATTTT | 11252 |
| rs116444532 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949179 | TTTTAACTTCTAAGC[C/T]ACCTTCTTACCAGCA | 11252 |
| rs116528292 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920453 | AGTTCCTCTGAATTT[A/C]TTTCTTTTCCAAAAT | 11252 |
| rs116534066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887149 | TCACCTGATCCCACC[A/G]TGGAGGCACCTGGGC | 11252 |
| rs116582319 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986599 | ACACTCTAATGGGGG[A/G]TGAAGATACACACTA | 11252 |
| rs116634802 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884861 | ACACGCCCATGTCCT[C/T]TTCTCCCTGTGGGGA | 11252 |
| rs116644175 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968236 | AACTAAACATCTGTT[C/T]CACTGTTGTTGTTTT | 11252 |
| rs116644341 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899074 | CATGCCAAGCTCTGT[A/G]GTGCTCCCAACCCCT | 11252 |
| rs116667734 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983842 | TGACTGGTGGTCAGT[C/G]TCCATCTCATGAGAC | 11252 |
| rs116726902 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014676 | CAGCTCTTAACCCCC[A/G]ACGGCCCTGCTCCTG | 11252 |
| rs116755929 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953855 | ATTGTGTGATTACAA[A/G]GACACTGGAGGAAAA | 11252 |
| rs116782174 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898842 | ATGAGGTGGCAGCTG[C/G]AATCTCAACCATCCC | 11252 |
| rs116817600 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909207 | CTACGGCACCTGGCA[G/T]GATGACCTGCCTAGT | 11252 |
| rs116836472 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985574 | GCCCTCGCTCGGCCA[A/G]CCCCTGAGAAGGACC | 11252 |
| rs116878654 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976502 | CAGGCCTCCCTGTCA[G/T]GCCTGGAGTGTCACA | 11252 |
| rs116910543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874686 | CTAGCAGCTCCCAGA[C/T]TACATATGGGGGAAC | 11252 |
| rs116944918 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886408 | AACCAGTCAGCAATG[G/T]TATGTATGTAGGTAG | 11252 |
| rs116960747 | snp | A/T | 0.0165278 | 0.0893908 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012798 | GCTGGGATTACAGGT[A/T]TGAGCACCACCACAC | 11252 |
| rs116964212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896353 | GAAGGTCACTCTTTC[C/T]TACTGCTAAGTAGTA | 11252 |
| rs117008677 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001032 | AGCCCTTGGGCCCCG[C/T]CCGACCTCAAATAAA | 11252 |
| rs117016593 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983605 | AAGAAAAGGACAATA[A/C]AAGATTGACATATGA | 11252 |
| rs117036995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994610 | GGGGTCTGGGGGTTA[C/T]TGGGGCAGGGAATTC | 11252 |
| rs117075846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947340 | ATGAGTCAGAGTGGC[C/T]CCAGGTCAACGCTTC | 11252 |
| rs117102323 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875860 | TGTATTTTTTGTAGA[A/G]ACAGGTTTTGCCATT | 11252 |
| rs117132112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959393 | TACTCGGTAAGAAAA[A/G]AATACAGCTAAAGTA | 11252 |
| rs117167479 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933820 | TCTTGGAAGTTATGA[A/G]TAAGATATTCTGATT | 11252 |
| rs117240531 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932868 | AGGACACCCCCCTGT[C/T]CACATGCCACTAGAA | 11252 |
| rs117240832 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940382 | CAAAGCAGGGGGTCA[C/G]CATGTGTTTGCTGAA | 11252 |
| rs117292628 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916546 | AACCACCTCACCCCT[A/C]CCACGGCACGCCGCA | 11252 |
| rs117301643 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901923 | TGGCTCGCCCCTGGC[C/T]CTTCCTCTCCGTGGT | 11252 |
| rs117306386 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984995 | GTTTGGCAACCAAAG[A/G]TCAGGAAAGCTGGCT | 11252 |
| rs117318653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42947001 | CACATACTTCCCGAC[A/G]ACGCCTCCTCTCCGT | 11252 |
| rs117354840 | snp | C/G | 0.039522 | 0.134904 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013420 | AAAGAGGCTACCAAA[C/G]TCTAGAATTAAGTTT | 11252 |
| rs117392913 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924236 | CCCCTGCATCTCTCC[A/G]CTGTCAGTGCCACTA | 11252 |
| rs117405349 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903122 | TACAAAGCTTTCAGG[A/G]AAATCCAGGGCCTGA | 11252 |
| rs117408258 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963203 | CCAAGGTCCCTGCCC[C/T]GGCCCACAATGTACA | 11252 |
| rs117421281 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927353 | GAGTTCAAGCAACTT[C/T]CATGTCTCAGCTTCC | 11252 |
| rs117480423 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969933 | AAAAGAAAAAAAAAA[A/G]AAAAGAAACTAGAAT | 11252 |
| rs117496814 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945454 | TGTCTGGCCCAGACC[C/T]GCATCTCTGCCTACT | 11252 |
| rs117551605 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902420 | AGTGGGTTCTGAGGG[A/C]AACTACTATGCCTCT | 11252 |
| rs117563155 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929111 | ATCCTCCCTACTTCA[C/T]CAGATCCAGGCCTGA | 11252 |
| rs117597236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936364 | GGTTCCCTTCCCTGG[C/T]TCCAGTATCAGTGGA | 11252 |
| rs117624337 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920722 | GGCAGGGTAGGAACG[C/T]CAAGCTCAGGGTTGA | 11252 |
| rs117632373 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908089 | CTCTTCATCTCCCCA[A/G]ATACTCTTCTCAGGG | 11252 |
| rs117641362 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934340 | AAACGCAAGACCTTC[A/C]AGGCACTGTGTGTGT | 11252 |
| rs117649709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919250 | TCAGCTATTTGTCCC[C/T]TCTGAGAGCCACTGT | 11252 |
| rs117682154 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005695 | TGGCAAATTCACTTA[C/T]GTAGACTGATAGGAG | 11252 |
| rs117753768 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916709 | GAACTCCCATGACTT[A/C]AAACGGCATCCATGT | 11252 |
| rs117767678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874514 | TGTGGGCAGGTAGGT[A/G]TGCACACACACAAGT | 11252 |
| rs117786234 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905322 | TGTGCGATGCTCCCG[C/T]GTGTGGCTGCAGAAA | 11252 |
| rs117847629 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015827 | CTGAGCACTGTCCTA[C/T]GCGCTGTCCAAGCAC | 11252 |
| rs117906401 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930322 | CTCTGCCCCAATTCC[A/C]CAGCCACAACATGCA | 11252 |
| rs117923688 | snp | C/G/T | 0.000486063 | 0.0155832 | missense | PACSIN2 | GRCh38.p7 | 22:42891165 | TCCAGGCCTTCTCCA[C/G/T]GGTCCCGTACTGGGG | 11252 |
| rs117935950 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942072 | GTGAGCCACTGTGTC[C/T]GGCCTTTATTATTGA | 11252 |
| rs117958712 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960603 | GAGAGAAAGATTTTA[A/C]AATGCTTGTGCCTAC | 11252 |
| rs117959559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002193 | GAAGCTAGAGATGAA[C/T]TCTAAAGGACCACAC | 11252 |
| rs117986523 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889098 | TAGGAAAAGTTACAT[G/T]CCAGAGTCAATTAGA | 11252 |
| rs118060347 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984151 | AATTTTTATGTTTTT[C/T]TGTAGAGACGGAGTT | 11252 |
| rs118112833 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935534 | AATGAAGTAACTGTA[C/T]TTAGGCAACACTTAA | 11252 |
| rs118124436 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948210 | AAGCTGCTGTGGCTG[G/T]GAAGGAGGGGAGAGG | 11252 |
| rs118125261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888907 | AGAGGGGAGAAAAAG[A/G]CAGGTACAAAATTGT | 11252 |
| rs118138848 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980154 | TATTGGGTGAAAATT[C/T]GTAAAATCTATAATT | 11252 |
| rs118169995 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973396 | CTTCCCCAGTGCTCT[A/G]AATTATGCAACTGGG | 11252 |
| rs118186437 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901760 | GAGGTGAGCCTTCAG[C/G]ATTCCAGGGTGTCTG | 11252 |
| rs137876228 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872798 | CCTCCCACTGTCGTG[C/G]CGCTTCTGCCAGACC | 11252 |
| rs137896944 | in-del | -/TACACACACACA | 0.456685 | 0.140646 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889372 | GGTTTTAATGGTTTT[-/TACACACACACA]TACACACACACACAC | 11252 |
| rs137903913 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974830 | GAAAGAAGAAGAAGA[A/G]GAGGAGGAGGAGGAC | 11252 |
| rs137908268 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903822 | TCCTCGGGGCCTCAA[C/T]TCTGTCTCAACTTGG | 11252 |
| rs137915543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934321 | ACAGCACAATTTCTA[C/T]GGGAAACGCAAGACC | 11252 |
| rs137923171 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911337 | ATGGCTTGAGCCCAG[C/G]AGATCAAGGCTTCAG | 11252 |
| rs137925469 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980010 | ATAAACCTATGAAAT[A/G]AGCGCATCATTGTTT | 11252 |
| rs137949779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992679 | CATCTTTTCACGACA[C/T]AGCATCTTCATTTGT | 11252 |
| rs138037794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900254 | TTCGGGTCACAGCTC[A/G]TCTCAAAATTGCCTC | 11252 |
| rs138043628 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004559 | TCTGTACAGGGAGCA[C/G]TGCCTGCTCTGTGGT | 11252 |
| rs138106937 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966703 | CAAATGCCACAGAAG[A/C]AGCAACATCTAGATT | 11252 |
| rs138140065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917937 | CTATGCTCTATCTTT[C/T]TATGCCTTAATGGTG | 11252 |
| rs138197642 | snp | C/T | 0.000364431 | 0.0134938 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891004 | GCCGTCCTCAGCTTC[C/T]TTGGTCTCCTTGAAG | 11252 |
| rs138222457 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938507 | CTCAGAAGCAGGTAG[A/G]GAATCTTTTTCTATG | 11252 |
| rs138233980 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961487 | TGTGTTTAGAAATTC[C/T]TTAGGCTGGGCCGGT | 11252 |
| rs138267401 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911566 | GCGGCAGATGCTCCA[G/T]CAAGTTTGAAGGCAT | 11252 |
| rs138269578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992989 | GGCAACACAGTGAAG[C/T]CCCGTCTCTACTAAA | 11252 |
| rs138274126 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873555 | CCTGGCTTCCCTGCT[A/G]AGTCAGGGGTTGGGG | 11252 |
| rs138277431 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982894 | AAAAAAAAAAAACAA[A/C]AACAAGGCTAGGAGC | 11252 |
| rs138288274 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931816 | CTTACACAATCCCTC[C/T]CTTCCAAAACAGCCC | 11252 |
| rs138290592 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887158 | CCCACCGTGGAGGCA[C/T]CTGGGCTGCTTCAAA | 11252 |
| rs138304512 | in-del | -/GTAT | 0.396546 | 0.202545 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886452 | TAGGTAGGTAGGTAG[-/GTAT]GTATGTACCTACCTA | 11252 |
| rs138312143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999521 | CTAAAAACACAAAAT[C/T]AGCCCAGCGTGGTGG | 11252 |
| rs138312154 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954133 | CCAGGCATGGTGACA[A/T]GTGCCTATAGTCCCA | 11252 |
| rs138338347 | in-del | -/AC | 0.263809 | 0.249618 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908037 | AACTCTTCAGGGCTA[-/AC]ACATTCCCAGAATAT | 11252 |
| rs138381234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986615 | TGAAGATACACACTA[A/G]AATCCACATGGGAAC | 11252 |
| rs138467670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885630 | CTCTCCTCTGACTCA[C/T]GTGGCTCAGAGCCCT | 11252 |
| rs138518656 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906175 | ACTGTCCCTGTCACA[A/C]TCACCTCTGTGTCCC | 11252 |
| rs138524371 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882915 | CTTTCTCTGGGCCTC[A/G]GTTTCCTCCTCCGTT | 11252 |
| rs138542738 | in-del | -/CA/TCCA/TCCATCCA/TCCATCCATCCA/TCCATCCATCCATCCATCCA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969043 | TCTTATCTATCTATC[lengthTooLong]TCCATCCATCCATCC | 11252 |
| rs138574030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957902 | AACAATTGACTGTCT[C/T]TCCCCTGAGCTAGGG | 11252 |
| rs138576311 | in-del | -/AG | 0.0221141 | 0.102801 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889490 | GGCCTCATGAGACAC[-/AG]ACAGTTTCATTATGA | 11252 |
| rs138589073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938019 | CTCTACCCACAGTTG[C/T]ACAGAGTAAAACAAA | 11252 |
| rs138633590 | in-del | -/TCA | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943115 | GTCTTACACTTCTCT[-/TCA]TAAATTTACTCCTAT | 11252 |
| rs138674700 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969886 | CTAGCCTGAGTGACA[G/T]GGTGAGATGCTGGCC | 11252 |
| rs138678743 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015920 | TAACTTGCTGGGGGT[A/G]ATGTGGAGTAAAGAG | 11252 |
| rs138688643 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966099 | ATCTTGGGCTGGGCG[C/T]GGTGGCTCACGCCTG | 11252 |
| rs138716237 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883642 | ACCTGATCACAAAGG[C/G]CCTCAAAGAAAGACT | 11252 |
| rs138768110 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897138 | GACAGGGTTTTGCCG[C/T]GTTGCCTAGGCTGGT | 11252 |
| rs138814745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903268 | TGGGGAGGGTGTGCG[C/T]GTGCCTGGCAGATGT | 11252 |
| rs138834734 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923306 | CTCAAAATGCAAGGC[A/C]GACCACATTGCTGGT | 11252 |
| rs138842796 | in-del | -/AAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913481 | CGAAACTCCGTCTCC[-/AAA]AAAAAAAAAAAAAAA | 11252 |
| rs138883709 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877426 | CAGTGTGGGAGGGGC[C/T]GGCTCCCATGGATGA | 11252 |
| rs138891181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953836 | CCTCTCAGAGGCAAG[C/T]GTGATTGTGTGATTA | 11252 |
| rs138892732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969467 | TTTAGATGCAAGTTT[C/T]TCTTCTTATGGAGGC | 11252 |
| rs138901031 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901296 | AAAGCTGACCAAATA[C/T]GCCAAGAAGCTCTAG | 11252 |
| rs138957341 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973201 | GAGAAAGCGAGAAGT[C/G]GTGTTTTTAAAACAA | 11252 |
| rs138958847 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012204 | ACATACATACATACA[A/G]ACATACAAAAACTAG | 11252 |
| rs138993882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960431 | GTCCCCTGGAGACAG[A/G]CAGGTGACCCCATGG | 11252 |
| rs139029603 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958575 | CAAGAAGGAAGGGAT[C/G]TGAAGAAAGAGATAT | 11252 |
| rs139045322 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912197 | AGTGGTTTTTAAATT[C/T]CCAAGGTAAAGAAAC | 11252 |
| rs139057580 | in-del | -/TGGGGGTTCACA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976451 | AAGCCTGACAAGTCC[-/TGGGGGTTCACA]ACAGGATCATCGATT | 11252 |
| rs139099494 | in-del | -/AAG | 0.0448719 | 0.142907 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993865 | AAGTCAAGAAATCAC[-/AAG]AAGAATGTGGCCCAA | 11252 |
| rs139108646 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898372 | TGCCTCCTTGGTTCA[A/G]GCGATTCTCTTGCCT | 11252 |
| rs139119326 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002839 | CGTCAACAGGATAAT[A/G]TAACCATTAATAATC | 11252 |
| rs139155473 | snp | A/C | 0.00112375 | 0.0236773 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909546 | GGCGGACGACCACAG[A/C]ACTGCGGAGTTGATA | 11252 |
| rs139184097 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892838 | CTTGAGAAACCCACA[C/T]TGCTCTGCTTCTGTG | 11252 |
| rs139254738 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001544 | AGCGCCTGGCAGAGC[A/C]AGTGCAGTCAGACGA | 11252 |
| rs139263470 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904969 | ACTACGGACCCCACC[A/G]GCTCTAAAATGAAAG | 11252 |
| rs139263651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984252 | GCTGGGATTACAGGT[A/G]TGAGCTACCACCCAC | 11252 |
| rs139288927 | snp | C/T | 0.00457996 | 0.0476341 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882174 | GCTCATGGGCACACC[C/T]TCCTCTTACCTCAAA | 11252 |
| rs139301476 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880500 | TACCCCTGACAGCAG[C/T]GCAGCCTCAGCTGAA | 11252 |
| rs139318777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916991 | GCTGCCACCTGCCAC[C/T]GTGACCTTGCCACCA | 11252 |
| rs139370376 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976204 | AACCCACCCACTGCT[A/G]ACCCTCCTCACTCTA | 11252 |
| rs139399039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010824 | GCAAACAGATGAACA[C/T]GCATTTATGGGAATA | 11252 |
| rs139450140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927592 | TTATTTAGTTATTTA[A/G]TTAGTTATTTTTGAG | 11252 |
| rs139450952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997806 | GAATCATCTGAACCC[A/G]TGAGGTGGAGGATGC | 11252 |
| rs139489068 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012160 | AAATAAATAAATACA[C/T]ACATACATACATACA | 11252 |
| rs139535211 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934544 | CCTTGCCCCTCATGG[A/G]CTGGCCCTGATAGCC | 11252 |
| rs139539457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964071 | GTACCCTTTAGCTAT[A/C]ATCCCTCTATTCCCA | 11252 |
| rs139549508 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993906 | TGAAGCACTCCTATG[A/C]AGCTGAAGAAGGGAA | 11252 |
| rs139579146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875306 | CAACACCACGCCCAG[A/C]TAATCTGCTACTTTT | 11252 |
| rs139593982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970325 | CTCTCCCCAAATTCA[C/T]CCACCAATCTAATAC | 11252 |
| rs139642820 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926826 | CCTGCCTCGGCAACA[C/T]AGAGAGACCCTATCT | 11252 |
| rs139667285 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989685 | TGCCTGTAGTCCCAG[A/C]TACTTGGGAGGCTGA | 11252 |
| rs139699425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945215 | CCGGCAATTACCAAG[C/T]TGACAGAAGCAAAAT | 11252 |
| rs139728514 | in-del | -/AC/ACAC/CCTCAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014321 | TGCTCCCCCCGCCCT[-/AC/ACAC/CCTCAG]ACACACACACACACA | 11252 |
| rs139776198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940847 | GGAGAGGCTGTGGGA[G/T]GGATGATGGGTGAAG | 11252 |
| rs139791037 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997959 | AACACCAGTGACCAC[C/T]GTTAGGTGAGCAAGG | 11252 |
| rs139822859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951123 | GAATACACTGATTGA[A/G]TTGCTTTTGAAAATT | 11252 |
| rs139824479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002021 | GTCAGTCCATGGGGA[C/G]GGGACATGGTGACAA | 11252 |
| rs139854279 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963935 | TTGAGATATAATTCA[-/AT]CGTCACACAGTTCAC | 11252 |
| rs139900147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940324 | AGTGAGTCATTAGAT[C/T]GTGACCTTATACTGT | 11252 |
| rs139914288 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888590 | CTATATGCCAGACAC[A/G]TCAACAACTGACACG | 11252 |
| rs139954070 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990428 | CAGTCCCCTGCCCTC[C/T]GCCTACCCAGCTCCT | 11252 |
| rs139985921 | snp | A/G | 0.000618153 | 0.0175697 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884357 | GTTGACTTCAATGAC[A/G]TGTGTGTTTTAGCTC | 11252 |
| rs139989254 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960009 | ACGCTCCTGCCTGCT[A/G]TGGCCATCACAGAAG | 11252 |
| rs140005966 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013811 | TATTTGGTAAACAGT[A/G]TACCAAGTAGCCCTG | 11252 |
| rs140022995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946215 | AGTGTTTAAACTGCA[A/T]GTGAGCATAACATAC | 11252 |
| rs140023047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993637 | TACACACATGAAAAC[C/T]GCATTGCCCTTATTT | 11252 |
| rs140060806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992474 | AGATGTTGGCCAAGT[A/G]CAGTGGTTCACACCT | 11252 |
| rs140077174 | in-del | -/AACTGGTTTGGGATGAAAAAT | 0.118933 | 0.212888 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954883 | ATAGAATTAAGAACA[-/AACTGGTTTGGGATGAAAAAT]AACTGGTTTGGATCT | 11252 |
| rs140086907 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902608 | TTTATCTGTCAGTTC[-/T]TTTTTTTTTTGAGAT | 11252 |
| rs140088197 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884991 | ATCAGATGAGGACAT[C/T]TCTCCTTCACAGTGT | 11252 |
| rs140105270 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997302 | AGTGGCTCACGCCTG[C/T]TATCCCAGGACTTTG | 11252 |
| rs140106770 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983809 | TTTAAGAATCTTTGT[A/C]TTTGTTCTTCAGTTA | 11252 |
| rs140108200 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928442 | TAGCTTCTAATTTCA[C/T]GCATCAGAGTACAGA | 11252 |
| rs140117606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871963 | CCATGTCTGACAGTC[A/G]TACCTGTCATTTTAT | 11252 |
| rs140129011 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904338 | GTCTCTGGGAAGACA[C/T]GCACTGCTCACTTGC | 11252 |
| rs140169471 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017411 | CATGTTGCCCAGGCT[C/T]GTCTTGAACTCCTGG | 11252 |
| rs140194669 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902355 | TTCCCCCACAGATTA[A/C]CCCTCCCCCTGGTGG | 11252 |
| rs140203556 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976740 | ACCAAACCCAGGTCT[A/G]ATCATTTCACAGATA | 11252 |
| rs140247706 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913617 | TACTAAGTACTGTTA[C/T]ACACCCTTAGTAAGT | 11252 |
| rs140249214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889337 | ATACTAGGGGGCAGG[C/G]CCATCAGCCACATTT | 11252 |
| rs140276319 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953447 | TTGAAGGGCCTAGCC[A/G]CTGCAATAAGAAAAA | 11252 |
| rs140306671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897706 | CTACTGAGGGACTCA[A/G]TGCTTGGGCACAGGG | 11252 |
| rs140377765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948123 | TCCCAGGTAGAGGAA[A/C]CTGTGTGACAAAGGG | 11252 |
| rs140381658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994319 | AAGCCCCATGTGTCA[A/G]ATAGGGAGGGACAAC | 11252 |
| rs140437504 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890063 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 11252 |
| rs140444232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875603 | TACAGTGGTGTGACC[A/T]TGGCTCACTGCAACC | 11252 |
| rs140445578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009826 | TTTTAAGGCTTCTTG[C/T]GAGGTCTTTGATAGT | 11252 |
| rs140470826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931132 | GTGTTGAGGGAGGCA[C/G]ACACCTAACTCACAC | 11252 |
| rs140487653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942463 | AAAGACTTATGCTAT[A/G]TTTTAAGAGTTTTAC | 11252 |
| rs140488927 | snp | C/G | 0.418974 | 0.184249 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014327 | CCCCCGCCCTACACA[C/G]ACACACACACACACA | 11252 |
| rs140500978 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004370 | ACTCTGCACCCCCCA[C/T]GCACATCCTCCTTGG | 11252 |
| rs140521113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899879 | TACATCAATTAAGAA[C/T]ACGTGCACATGAAGT | 11252 |
| rs140529965 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951458 | TCACTCAGCCTCTCC[A/C]TGAGCTCCAGATCCG | 11252 |
| rs140532601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936973 | TATTTACACCCATTG[C/T]GAATGCATTAGTAAT | 11252 |
| rs140534318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956964 | AGAAAAGGAAGCCGA[C/T]TGGAATATTCTATAC | 11252 |
| rs140591355 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996551 | AAAAAAAAAAAAAAA[-/AA]TTGGCCAGGTATGAT | 11252 |
| rs140601276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969477 | AGTTTTTCTTCTTAT[A/G]GAGGCCTTGGGGAAG | 11252 |
| rs140636930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896379 | TAGTATTCGATTGTG[C/T]AGTTATGCCACTATC | 11252 |
| rs140643266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968243 | CATCTGTTTCACTGT[C/T]GTTGTTTTGGGGAAG | 11252 |
| rs140659403 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919892 | AAGGCCAAAGCAGGT[A/G]GATCACTTGAGGCCA | 11252 |
| rs140662623 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950153 | TTGTCATTATTCCCT[A/C]AACAATACGGTATAA | 11252 |
| rs140709033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908071 | ACACAAGATACTTAT[A/G]TTCTCTTCATCTCCC | 11252 |
| rs140727855 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905948 | ACCTGACCACCCACC[A/G]CCACCCACTCCTTCA | 11252 |
| rs140752551 | snp | C/G | 0.00087797 | 0.0209336 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876189 | ATAGTCATACAGGGC[C/G]CGGACTCGCACTTCC | 11252 |
| rs140818308 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881148 | GGGCCCACACTGTCA[C/T]TTGGAAAAACCTTCC | 11252 |
| rs140822448 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956314 | CTTATGATTCATATA[C/T]GACAGAGTCTAATAA | 11252 |
| rs140850962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955731 | CATTCTTCCTGCACA[C/G]TAATGGTAGGATCTG | 11252 |
| rs140853278 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905234 | TGATGGCATTCACAC[A/G]GGGGGAAGACAGGTC | 11252 |
| rs140875356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986404 | TTCATCCGGCCAAAC[A/G]AAATCAAACGCCTAA | 11252 |
| rs140943057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967989 | AGATCTTTATATACA[A/G]TGATATACTCAGGAT | 11252 |
| rs140951408 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995433 | ACAAATGTTGTTTCA[C/T]TGCACCCTCCGTCCA | 11252 |
| rs140977423 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978610 | GTTTCCATGCCCGCA[C/G]TGACGGTAAGTTGTG | 11252 |
| rs141010635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937702 | CCTAACTCGGCTCTC[C/T]CTCAGACTCAACCAA | 11252 |
| rs141018959 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890631 | GCTGAGGCAGAATTG[C/T]TTGAACCCAGGAGGC | 11252 |
| rs141025735 | snp | C/T | 0.0471551 | 0.14613 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996015 | CACAAGGTCAGGAGA[C/T]CAAGACCATCCTGGC | 11252 |
| rs141039354 | in-del | -/TTAT | 0.0209421 | 0.100162 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875366 | GCTCTGTTGCCCAGG[-/TTAT]TTATTTGTTTGTTTG | 11252 |
| rs141121348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929488 | CAGTGGATTGTGAAA[C/T]GTTCAGTGGGAGTGG | 11252 |
| rs141124387 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007251 | TGAGACAGTCTCGCT[C/T]TGTCACCCAGGCTGG | 11252 |
| rs141169351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896590 | ATAAAGAAGCTATAA[C/T]GTTCATCTATTGGTC | 11252 |
| rs141184922 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968742 | CAGGAAAAGGGCAAA[C/T]GTGTCTATCAATGTC | 11252 |
| rs141200152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983036 | AAATACAAAAATTAG[G/T]CCGGGCACAGTGGCT | 11252 |
| rs141206555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938937 | AACCCTTAAAATAAC[C/T]ATGTTTTCCCCAACA | 11252 |
| rs141230475 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898986 | TCCTCCATCCTGCAT[C/G]CATCTGTTGTAAACA | 11252 |
| rs141234763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892647 | CACAGCCTGGGCACA[C/T]ACCCTGCCCTAAGGA | 11252 |
| rs141299384 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011677 | AGGTCAGGAGTTCCA[C/G]ATCAGCCTGGCCAAC | 11252 |
| rs141356939 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008764 | GGGCCTCCTAGACTG[A/C]AGAAAGCATCTCATC | 11252 |
| rs141385918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933758 | AAGTGGCAGAACAAC[A/G]GACTTTTCCCATTTG | 11252 |
| rs141393049 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886365 | AGATGTAGTTGATGG[A/C]TGATAAGAAACATGA | 11252 |
| rs141395971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961281 | TAGGTTAAAAATCTC[C/T]TTTGAAAATCTTGTG | 11252 |
| rs141480477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903351 | TTTCTTCCAACCTAT[A/C]CTAACCCCTATGCTG | 11252 |
| rs141488058 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979211 | CTGTTTGTGTTTTTA[C/T]TTATAGATTTACAGA | 11252 |
| rs141571691 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950970 | TGAAGCCAAGTGGGG[A/G]ACAGAGAGTGACAGG | 11252 |
| rs141578769 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904506 | CCGGTCCCTAAGCTC[A/G]CTGAAGACCTGAGGC | 11252 |
| rs141610192 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904239 | TGTTACACAGATGTC[C/G]AGAAGGCCCCGCGAC | 11252 |
| rs141671248 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911518 | AACAAAAATAATCCA[A/G]TCAGGAAGAGGGCCA | 11252 |
| rs141674078 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870528 | AGCATCTTTACAGAT[A/G/T]CATTTGCTTGAAAAG | 11252 |
| rs141680831 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906501 | CAAAGGCAGCCCACA[C/T]GTCGAGGGCCCTGAT | 11252 |
| rs141700457 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882593 | GGTGGGCTGTGTGGG[C/T]CACCACTCTGTGTGG | 11252 |
| rs141706841 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901897 | CCTTCCGTGGTTCAG[C/T]TCGGACCAGCTGGCT | 11252 |
| rs141715307 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966236 | TTAGCAGGGTGTGGT[C/G]GTGTGCACCTGTAGT | 11252 |
| rs141716644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926570 | AAGAAACACAGCACA[A/G]ACTCTCCAATATCTC | 11252 |
| rs141718130 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003335 | ATATCGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 11252 |
| rs141720754 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959254 | CTCTCTCAAGTCCCA[C/G]TTATGTGTTTGTAGA | 11252 |
| rs141725799 | in-del | -/AAG | 0.0322114 | 0.122752 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897301 | TAGTTTTTACAATGC[-/AAG]AAAATTAATTTTCAA | 11252 |
| rs141731031 | in-del | -/ATATATATAT/ATATATATATAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975457 | AAAAAATATATACAA[-/ATATATATAT/ATATATATATAT]ATATATATATATATA | 11252 |
| rs141787390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969704 | AGCACTCTGAGAGGC[C/T]GAGGCATGATGATCG | 11252 |
| rs141828815 | in-del | -/GAC | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948851 | AATGAATTCTAACTT[-/GAC]AGTGCTTTTATTTCT | 11252 |
| rs141862500 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962769 | GTCACAAGAGCAAGG[C/T]GTGGGCGGGGGGGGG | 11252 |
| rs141863372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999362 | GTGTATGTGTGTGTA[C/T]GGAGGCATTAAAAAA | 11252 |
| rs141899828 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921482 | GATGTGGCCACTCTC[C/T]CATTTAGGGGAAGGG | 11252 |
| rs141925739 | in-del | -/ATAATC | 0.452103 | 0.147154 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965941 | ATCATAAATAAATAA[-/ATAATC]ATAAATAAATTATGT | 11252 |
| rs141956945 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877213 | AGGAGCCTAGGAGAG[G/T]ACTTGGTTTCCCTTT | 11252 |
| rs142001146 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907738 | CTGCTCTCCATACAA[C/T]GCTGGCTCTAGGAGG | 11252 |
| rs142003196 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989456 | TGAGCCGAGATCACA[C/T]GATTGCACTCCAGCC | 11252 |
| rs142028768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923322 | GACCACATTGCTGGT[A/C]TTAAGTCCCTTGTGC | 11252 |
| rs142079730 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002299 | CTAGAGAAGGTCTGT[A/G]AGATACCTACCGCGA | 11252 |
| rs142091254 | in-del | -/TTTT | 0.0399052 | 0.1355 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943622 | GGTGTTTTTTCTTTC[-/TTTT]GTTTTGTTTTAATGT | 11252 |
| rs142091342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925877 | GGCCCATGGGTCCCT[A/G]GGCCCTCTATGTCAC | 11252 |
| rs142111865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988349 | AGGGGTGGGGGGCAC[A/G]TCATGGCCAGAGCAG | 11252 |
| rs142129423 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947715 | CAGCTGCCTCAGGCA[A/C]AATACCTAAGAGCTC | 11252 |
| rs142131076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900894 | GGGATCAGAGCTGGT[A/G]TAAACTGAGACTTAC | 11252 |
| rs142192403 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902988 | ATCAACTCTTAGCAC[A/G]TCATCAGCCAGTAAC | 11252 |
| rs142195883 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991635 | AGCTGGGAACTCCCA[C/G]GTGCGATAAAGAGAA | 11252 |
| rs142212309 | snp | C/T | 0.000576963 | 0.0169749 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884460 | GCGAAGGCGTTTCTC[C/T]TCGAACTGCTGGCAC | 11252 |
| rs142257943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984096 | CCACTTCAGCCTCCT[A/G]AGCAGCTGGGATCAT | 11252 |
| rs142265337 | in-del | -/GGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923035 | GTGAGTGTTGTGGCT[-/GGG]GTCCCAGCACCCAAC | 11252 |
| rs142280754 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015391 | CGCAGATTACTCTCC[C/T]AAAGCCGCTCGCTGG | 11252 |
| rs142314308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943235 | ATTTTTGTATATTGA[C/T]CTTATATCCTACAAC | 11252 |
| rs142332762 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955757 | ATCTGACTAAGTGAA[C/G]CTGAGGTGACCGTCC | 11252 |
| rs142340923 | snp | C/G/T | 0.0201678 | 0.0984315 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985309 | TCCAGCACTCCAGCT[C/G/T]TGGCGACAGAGCGAG | 11252 |
| rs142354837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941701 | TATCTTTGAAGAAAC[A/G]TCGGTTTAGATCCTT | 11252 |
| rs142415626 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924517 | GCTCTTAAGCCCCCC[-/A]ATGCAGAGTAAAAGC | 11252 |
| rs142439621 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944062 | CTAAGCCAGACTGTG[A/T]TGGTAGTCCTGGCCA | 11252 |
| rs142466719 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010774 | CCTTATTCTAGGAAA[C/T]AAGAAAGACTCTATG | 11252 |
| rs142491294 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889639 | GGCGGAGGAAGGCAG[C/T]GCAAGGCCAGAGAAC | 11252 |
| rs142494930 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964182 | CAGTACTTTGTGGGG[A/C]CAAGGTGCGCAGATC | 11252 |
| rs142495115 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916825 | GACGAAGTCACCTGG[C/T]ATACATCTGACACCC | 11252 |
| rs142499636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872924 | GTGCCTCGGGCCCCT[A/G]GCGTTTCTTTTGTCC | 11252 |
| rs142501884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949133 | TCCTGTCTCTATAAG[A/G]ACAAAACATTTCTTA | 11252 |
| rs142526002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963399 | GCCCCCTGCAGAGGC[A/G]GCAAACAACACGCAG | 11252 |
| rs142531616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004684 | ATGCTCACAAACTAC[A/G]GTTTGGGTATCACTT | 11252 |
| rs142570501 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006673 | TACAAAAATTAGCCC[A/G]GCATGATGGCGCATG | 11252 |
| rs142585451 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940668 | TTCAAGCTGGTGAAG[-/C]CCCCTGCCACCGCCA | 11252 |
| rs142667137 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961012 | ATGCACACTCCCCCA[C/T]TCCCCTTGGCAAGCC | 11252 |
| rs142673204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001558 | CCAGTGCAGTCAGAC[A/G]AGCCCTGAAGTGTGG | 11252 |
| rs142678729 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898140 | GAGCCAAAAAAGGGA[A/G]CTGCCCATCCTCCAG | 11252 |
| rs142680741 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970020 | GAAAACTGTAGAATG[C/T]TCACAAAATCACAGA | 11252 |
| rs142682743 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016120 | CGAGGCAGGAGAATC[A/G]CTTCAGCCCAGGAGT | 11252 |
| rs142684726 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952460 | GCCTCCTTGGTTCAA[A/G]CGATTCTCCTGCCTC | 11252 |
| rs142757987 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012577 | CTTCCATCTCCCAGG[G/T]TCAAGCAATTATCAT | 11252 |
| rs142834966 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887532 | TGCAGCCTCTCTCTA[C/T]CTCATTCCGTCTCTC | 11252 |
| rs142856353 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966054 | TGTTAGCCTTTCATA[A/T]GTTTCATGAACCAAG | 11252 |
| rs142869799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901383 | ATTCCAAGTCTGCAG[C/T]TGGCAACGAGACGGG | 11252 |
| rs142877414 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902770 | AGACATGCACCACCA[C/T]GCCTGGCTAATTTTT | 11252 |
| rs142877484 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978434 | CAGTCTTCGTTTACA[C/T]GCAACACAAGAAGAG | 11252 |
| rs142894255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891357 | CCCAAAGCTGAATTT[A/G]CTCTGCCCCTCGTGT | 11252 |
| rs142920143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949601 | CAATAATATTATCTG[A/G]GAAGCCCTGAAGAAA | 11252 |
| rs142938283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928858 | GCCAAAATTTAGAAG[C/T]CTCATCCCAAATTTG | 11252 |
| rs142948859 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982554 | CTTCTGCCTTGGGAT[-/C]CTGTTGATCTGTGAC | 11252 |
| rs142962979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912318 | GTAGACTCTAATCAA[C/T]TCTGGGCACATATGT | 11252 |
| rs142999927 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870164 | TGTGCACAAGTAACA[C/T]GACGACTGAAATCTG | 11252 |
| rs143016245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982984 | TCACGAGTTCAAGAC[C/G]AGCGTGGCCAACATG | 11252 |
| rs143030609 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993489 | TCTTATTTTGCCAAG[G/T]AAGAATATCCTTTAG | 11252 |
| rs143037485 | in-del | -/TTTC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934900 | TTCTCTTTCTTTTCT[-/TTTC]TTTCTTTCTTCCTTT | 11252 |
| rs143062448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944924 | CCAACACAGTGAAAC[A/C]CTATGTCTACTAAAA | 11252 |
| rs143074772 | snp | A/C/T | 0.0126979 | 0.078662 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016920 | TTTGGGAGGCCGAGA[A/C/T]GGGCGGATCACGAGG | 11252 |
| rs143078201 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916713 | TCCCATGACTTCAAA[C/T]GGCATCCATGTGCAG | 11252 |
| rs143148433 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932711 | TGTTTATTGAGCTGA[C/G]AGCAAAACAATTTTT | 11252 |
| rs143185556 | snp | A/C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871147 | ATTTCTGTTGTTCTG[A/C/T]GTCTTCCTGCGCTCA | 11252 |
| rs143195124 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956315 | TTATGATTCATATAT[A/G]ACAGAGTCTAATAAG | 11252 |
| rs143195654 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973156 | ATTCCTATCCAAAAT[G/T]CCCTGCAACAAATTA | 11252 |
| rs143257796 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003684 | ACAACGTTGACAAAA[C/T]GTGAAGACCTTTCGC | 11252 |
| rs143290312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917206 | AGCTTGCCCAAGCAG[C/G]GGAGTTGAGACCTTA | 11252 |
| rs143292304 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874241 | ACTGCTTGAGCCCAG[A/G]AGATCAAGGCTGCAG | 11252 |
| rs143308486 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996362 | GATGCTGAAACCCCA[C/T]CACTACTAAAAATAC | 11252 |
| rs143346816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919163 | TTGGGGGCTTCTCAT[C/T]TGGAAGGTAAAGTTC | 11252 |
| rs143355880 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877738 | AAGACCACAGGCAGA[A/C]CATCAAGCAATCCAA | 11252 |
| rs143363776 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998937 | CAAACTCCAGGAAAA[C/G]ATCACCTTCCCACTC | 11252 |
| rs143390561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934329 | ATTTCTACGGGAAAC[A/G]CAAGACCTTCAAGGC | 11252 |
| rs143393089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885887 | AAAGAGCTCCACAGC[A/G]CTGTGGCTATTCCCC | 11252 |
| rs143434815 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016256 | GAATTGCTGCTACAT[A/G]TAGATAGGTATGAGA | 11252 |
| rs143473728 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956780 | TTTAACCCCTTCTCA[A/G]TTTGGAGCAATGCCA | 11252 |
| rs143482042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960071 | ATTTCAGTATTTCCA[C/T]GGAAAATCAGGGAGA | 11252 |
| rs143492651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882014 | ATGCCTGCAGCCCCC[C/G]AGGACTCTATGCCAG | 11252 |
| rs143510810 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943714 | ATATTTTGATGAATT[C/T]CAAGTGTCATAAGGA | 11252 |
| rs143556689 | snp | A/G | 0.030278 | 0.119257 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899340 | TGCCCAAGCTGAAGC[A/G]CAGTGGTGCCATCTC | 11252 |
| rs143570021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897248 | GGCCTGTTCCCTTTT[A/T]AATATATTTTTTAAA | 11252 |
| rs143573507 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969544 | CAATAACTCTGGCAA[C/T]GATGACCATTGTAAC | 11252 |
| rs143607534 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905654 | GCTGAGCACGCAGGC[C/T]GAAGACAATGTTGTA | 11252 |
| rs143623402 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017422 | GGCTCGTCTTGAACT[C/T]CTGGGCTCAAGCAAT | 11252 |
| rs143674618 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965423 | TACCTCAATAAAGAG[C/G]AAGAAGGCGGGAGAA | 11252 |
| rs143716961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013957 | GGCACCCAAGCCAAG[A/T]GTGGCATCCCCAGGT | 11252 |
| rs143717855 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892907 | TGGGAAGTGTGTTCT[A/T]AGCATGGCCCCTGTC | 11252 |
| rs143724297 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948212 | GCTGCTGTGGCTGTG[-/AA]GGAGGGGAGAGGGGA | 11252 |
| rs143726243 | in-del | -/TATTTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009864 | TCATTTTATTTTTTC[-/TATTTTTT]TTTTTTTTTTTTTTT | 11252 |
| rs143763635 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972746 | AGTCAGCCATGCTTT[-/T]ACTTTTTTTTTTCTT | 11252 |
| rs143768564 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940360 | TCTCTGAATCTCAGA[C/G/T]GCTGTGCAAAGCAGG | 11252 |
| rs143782532 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897349 | ATCATACATTAAAAT[A/C]AGCACATATATAGTT | 11252 |
| rs143808263 | in-del | -/AAAAAAAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926385 | CAGAGATTAAAAAAA[-/AAAAAAAC]CAGCCAGCATCTCCA | 11252 |
| rs143809609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999849 | AAGCTTCTCTGAGCC[C/T]ATTTCCTCAACTGTA | 11252 |
| rs143809628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955205 | AACTCAATCCTAACC[A/G]TCTATGGATCCCTAG | 11252 |
| rs143816473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921502 | TAGGGGAAGGGCCAA[C/G]AGGGAACCAGCTCAG | 11252 |
| rs143900335 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977351 | AAACAATCCAGTAGA[C/T]GGAAAAACGGAGAAA | 11252 |
| rs143909586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967197 | AGGAAGGCTGGACTC[C/T]GAGCTGAATCACGTA | 11252 |
| rs143920193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996837 | GATCAAAACCACACA[A/T]CACATTTCCTAGGTA | 11252 |
| rs143937466 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965293 | TGGGGGACTGACTTC[-/A]AAGGGACACAAGGAA | 11252 |
| rs143959063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904152 | AAAGGATGTGTTTAC[A/G]CAAAGCTGTGTTGAA | 11252 |
| rs143960005 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012206 | ATACATACATACAAA[C/T]ATACAAAAACTAGCC | 11252 |
| rs144004027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913759 | CAGTAATTTGCCCAC[A/G]GTTGTCCAAGTAATG | 11252 |
| rs144006164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994745 | TGGAAAAAGGGCCCC[A/G]GGCAGGGGTCCCACA | 11252 |
| rs144052307 | in-del | -/CCCAGGGCCCCGG | 0.0763149 | 0.179815 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871847 | CTCTTCTGTCCCCTC[-/CCCAGGGCCCCGG]CCGCCTTGCTCCCAG | 11252 |
| rs144074003 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883307 | CCACTTTACAAGACT[A/G]TCATAAAAATGGAAT | 11252 |
| rs144079616 | snp | C/T | 0.123105 | 0.215401 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883856 | TAAAAATACAGAAAT[C/T]AGCTGGGTGTGGTGG | 11252 |
| rs144080380 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958095 | CGGACTCATCAGTAG[A/G]AAAAAAAAACACTCT | 11252 |
| rs144099446 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923618 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTC | 11252 |
| rs144146071 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919654 | AGCATGCGCCTGTAA[C/T]CTCAGCTACTCAGGA | 11252 |
| rs144147139 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997917 | ACAAGTGAAGAAACA[C/T]TGCTGAGTTCCACCC | 11252 |
| rs144151764 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880531 | CTGCTAGGAGCCTAG[C/T]GGGGGCAGCACACCC | 11252 |
| rs144216502 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937076 | TGAATGCTGGGAATC[C/T]AACAGCGGAGAGAAC | 11252 |
| rs144229512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011526 | ATATTCCACAACATC[C/T]GGAATCATCCACTGA | 11252 |
| rs144265799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918910 | AGCTGAAGAAACACA[C/T]AAGCTGAGGAGACTG | 11252 |
| rs144298781 | snp | A/G | 0.000780361 | 0.0197376 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879107 | GCCCGTCAGGGTGAC[A/G]CCGTCAGTGGCCTTC | 11252 |
| rs144299622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964105 | CTTTCCCCAGCCCGC[A/G]GCAGTCATTGTGTTT | 11252 |
| rs144305526 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010018 | GAGATTATAGGCGCA[C/T]GCCACCATACCCGAC | 11252 |
| rs144313814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967478 | GGTAATACAACCCCA[C/G]AATCAATGAAAAGCC | 11252 |
| rs144330664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976310 | TTCCTGGTTCCTATA[A/G]AGCAAGGCCAGAAGC | 11252 |
| rs144364137 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934943 | TTTTTTGAGACAGAG[C/T]TTCGCTTTATCGCCC | 11252 |
| rs144399384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874020 | GTCTCAAACTCCTGA[A/C]CTCAAGTGATCCTTC | 11252 |
| rs144402440 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950182 | AACTATTTACATTGT[A/G]TTTATATTCTATTAG | 11252 |
| rs144456824 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012937 | GGAGATTACAGGCGT[G/T]AGCCACCACGCCCGG | 11252 |
| rs144461288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901395 | CAGTTGGCAACGAGA[C/T]GGGCAAAATGCTTTC | 11252 |
| rs144493239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941400 | TTCATTTCTTTTGAG[A/T]AGATACCTAGGAGTA | 11252 |
| rs144509444 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898720 | AGGACTCGCCCTGCC[A/G]CCTGCCCTCCTCCAG | 11252 |
| rs144547235 | in-del | -/ATTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979928 | AATTTACATACACAC[-/ATTT]ATTACACATACGCAC | 11252 |
| rs144575235 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888910 | GGGGAGAAAAAGGCA[G/T]GTACAAAATTGTATG | 11252 |
| rs144584550 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870433 | TTAAATCTCATTAAA[A/G]CAGTAGACGAGTGCT | 11252 |
| rs144604261 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894064 | TGTAAAAACTTTTCC[-/A]ACTTCCTGAGCACCT | 11252 |
| rs144633031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995451 | CACCCTCCGTCCACT[A/G]AGGAGACAAGGTTTT | 11252 |
| rs144633087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949462 | CATACACACACGCGC[A/G]CGCACGCACACACAC | 11252 |
| rs144671532 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017559 | TCCACACACCGCATG[C/T]TCACTGGTCTCACCA | 11252 |
| rs144673224 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873474 | CAGCAGGCTGGCACT[C/G]TGGGTGCTGAGGGGA | 11252 |
| rs144688978 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952671 | CCTATTTATTTATTT[A/T]TTTTTTTTTGAGATG | 11252 |
| rs144707407 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883714 | AGTGGATCTTACATA[C/T]GCCAGCTGCGGCCAG | 11252 |
| rs144709359 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958810 | CGGAGAGAGGATGCT[G/T]CCTTTTTAATGGCAA | 11252 |
| rs144713575 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905321 | GTGTGCGATGCTCCC[A/G]CGTGTGGCTGCAGAA | 11252 |
| rs144729827 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989756 | CAGTGAGCTGAGATC[A/G]CGCCACCGCATTCCA | 11252 |
| rs144778161 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012865 | CTCCATGTTGGTCAA[A/C/G]CTGGTCTCGAACTCC | 11252 |
| rs144789952 | in-del | -/TC | 0.0185938 | 0.0946107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942859 | GCCCTCCAACTTTGT[-/TC]TCTGACTTTTCAAAA | 11252 |
| rs144806979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898551 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 11252 |
| rs144810952 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970849 | GTGGTAACAAGCAGT[A/G]CTGACCATGAGATGG | 11252 |
| rs144818225 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953904 | AAGGAAAGCCAGGGA[A/G]GAGAGGAATGCTTAG | 11252 |
| rs144826918 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008439 | TATTTTTAGTAGAGA[A/T]GGGGTTTCACCATAT | 11252 |
| rs144845457 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954615 | TCCAGACTGGTCTCA[A/G]TGACTTTTTAATTTT | 11252 |
| rs144850270 | snp | A/C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968142 | CCTGGCTCCCTCTGA[A/C/T]GGCCGAGTGTGTCCT | 11252 |
| rs144851731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907275 | GGTGATGCAGAAAAC[C/T]GAAGCTTCCCAGCAG | 11252 |
| rs144870772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910632 | TGAGATGTGGCTGGC[A/G]ACCTGTTTGGCTGTC | 11252 |
| rs144884226 | in-del | -/GAGAGGGAGGGAGGGAAGGA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950402 | ATACCAGATTAGGCT[-/GAGAGGGAGGGAGGGAAGGA]GAGAGGGAGGGAGGG | 11252 |
| rs144885300 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915159 | ATGGATGAGCCACCA[C/T]ACCGGGCCTAAGATT | 11252 |
| rs144934439 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960484 | CCTAAGAACTAGGAC[A/C]CTCAAATACGCAACT | 11252 |
| rs144988057 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910223 | GAGTGTGCTTGTCCT[G/T]TCTGCACCACCACCA | 11252 |
| rs144996422 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991163 | ACCACCTCCTAGGAA[A/G]CTGCTGTACAATGGT | 11252 |
| rs145000608 | snp | C/G | 0.0836354 | 0.186609 | utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015034 | ACCTCCCAATCCGTC[C/G]CACACTCCGTTCAGG | 11252 |
| rs145052606 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892242 | GCCGGGGCAGAAATC[A/G]AGAAGATCCATGGCT | 11252 |
| rs145058557 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896969 | TGAGACAGGGTCTTG[C/T]TTTGTTGCCCAGGCT | 11252 |
| rs145121483 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924819 | TGAAGCGCAGTGGCA[C/T]GATCTCAGATCACTG | 11252 |
| rs145133810 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927720 | AGCCTCCCGAGTAGC[A/T]GGGATTAGAAGCATG | 11252 |
| rs145144755 | in-del | -/CAGT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941218 | CCACGTTGCAGCATG[-/CAGT]TGTATTTCACTCCTT | 11252 |
| rs145179845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984785 | GGCAGAAAACATCCC[C/T]AAGACTAAGAGCACA | 11252 |
| rs145199703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968620 | TGTCCATGGGGCTGT[C/T]TCCAGAAGAGACTAG | 11252 |
| rs145276571 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872094 | CTCTAATGTATTAAC[A/G]TGGTTCCATTTATCT | 11252 |
| rs145301567 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906502 | AAAGGCAGCCCACAC[A/C/G]TCGAGGGCCCTGATC | 11252 |
| rs145367209 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911196 | GACATGAGCCACTGC[A/G]CCCGGCCATGCAAAG | 11252 |
| rs145399409 | in-del | -/TTTTCT | 0.0343294 | 0.126436 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917786 | CACTGATTGGTACTC[-/TTTTCT]TTTTCTTTTTCTTTT | 11252 |
| rs145430465 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870545 | ATTTGCTTGAAAAGT[G/T]AGTCTTCTTTTTAAC | 11252 |
| rs145446015 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946755 | AGAGCACATGAGGAC[A/G]CGTCAGCTCATCTCT | 11252 |
| rs145448014 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993732 | AAGGCCGACCAGAGC[C/T]GAAGGACACTCTCCG | 11252 |
| rs145460862 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951281 | ATTCTCTCTAGACAA[A/G]TAATTCCGGACAGTC | 11252 |
| rs145493254 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920275 | TGAACTCACTCTCAC[A/G]GGCTACCCTGGGTGC | 11252 |
| rs145495429 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874976 | CTGCGTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 11252 |
| rs145527779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998784 | CCTTTCAGCCCACCA[A/T]GTCCCCCATCATCCT | 11252 |
| rs145554651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875496 | CACCTCAGCCTCCCA[A/G]AGAGCTGGGACTACA | 11252 |
| rs145556282 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951576 | TGCATCCCCCGGTTG[A/G]GCTCCTCCAGGACAC | 11252 |
| rs145572380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011759 | GCAGGCGCCTGTAAT[C/T]CCAGCACTTTGGGAA | 11252 |
| rs145596059 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007052 | CCTCCCCCATCTGCA[A/T]CCCTGACTTCTCAAC | 11252 |
| rs145601109 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994226 | GTGGCTGGTTTGGTG[G/T]TAAGAAGGGCTGAGC | 11252 |
| rs145653318 | snp | A/G | 0.0021201 | 0.0324893 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890898 | GGTGCTGCTAGTGGG[A/G]TGCCAGGCAGAGCAA | 11252 |
| rs145667839 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926265 | TAAAGGCTGGCCCCT[C/T]CCTCAAGGGAATCAC | 11252 |
| rs145670773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004481 | TGCGAGCTAAGTGGC[A/G]AGCAGGCAGCCAGCT | 11252 |
| rs145687758 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003394 | GGCGGATCACGTCAG[A/G]AGATAGAGACCATCC | 11252 |
| rs145707016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931487 | GTCCGAGACAGAAGA[A/G]ACCTTAGGTGATGGG | 11252 |
| rs145714915 | snp | C/G | 0.00279258 | 0.0372817 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007565 | AGAATGGTCCTTCAC[C/G]TCAGCCCCACCTGGA | 11252 |
| rs145715435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008107 | TGTGTGCAGTACTAT[C/G]AGCTTCCATGTCTGA | 11252 |
| rs145783860 | in-del | -/TC | | | | | GRCh38.p7 | 22:42887542 | CTCTACCTCATTCCG[-/TC]TCTCTCTGCAAATCC | 11252 |
| rs145836663 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992777 | TGCATTGGATTTTTT[A/T]AAAAATGAAACTAAC | 11252 |
| rs145849018 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890775 | GCATCTTCAACCTGG[A/G]TAAATGTCAACTACC | 11252 |
| rs145991993 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902341 | TGCCCCAGGACGCTT[-/C]CCCCCACAGATTACC | 11252 |
| rs145992566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959319 | TGTAATAAACATTAA[C/T]GCCTTAAAGTAGGGG | 11252 |
| rs145995007 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004979 | TATGGAAAGCTTCTT[C/G]GTAAAATGCAAATGC | 11252 |
| rs146009921 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888239 | TCATAACCCTCCATA[C/T]CAGCTCACACCACAC | 11252 |
| rs146014246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961690 | AGGCACGAGAATCGC[C/T]TGACCCCAGGGAGCA | 11252 |
| rs146014681 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903074 | CACATAAGCACAGCC[A/G]GCTGCAGGGCCTCAC | 11252 |
| rs146019870 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001709 | AGCTTTTCTTAGCTG[G/T]GATAAGAGGAACCAA | 11252 |
| rs146036504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884199 | CCATGCCTGCAGCTG[C/T]AGAAACACTCAGCAG | 11252 |
| rs146069723 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943325 | TATATAAGATCATGC[C/T]ATCTTTGAACAGAGA | 11252 |
| rs146133451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904288 | ATGCACAGCATATGC[C/T]GCCCTGTGTGCCATC | 11252 |
| rs146143971 | snp | A/G | 0.0444908 | 0.142359 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017153 | GACTCCGCCTCAAAA[A/G]AAAAAAGAAATACAG | 11252 |
| rs146159223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902331 | GGGGGCTCTGCTGCC[C/T]CAGGACGCTTCCCCC | 11252 |
| rs146197559 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901139 | CTGTGGCCCTGAAGG[C/T]CCAAGCACCACAACC | 11252 |
| rs146208274 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011736 | ACAAAAACTAACCAG[G/T]CAAGGTGGCAGGCGC | 11252 |
| rs146236694 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919409 | TCCAAGGACAGGGAC[G/T]CATCTGGCACTTCTT | 11252 |
| rs146262532 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963204 | CAAGGTCCCTGCCCC[A/G]GCCCACAATGTACAG | 11252 |
| rs146266878 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988898 | GAAATTTTTTTTTTT[G/T]TTTTTGGGAGTGAGT | 11252 |
| rs146357529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940429 | TGTCAACAGGAATAC[A/G]GATTACACCAGGTAG | 11252 |
| rs146357582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988451 | ATTAGTTAATCCTGC[A/G]TCCTAGTAATTAAAG | 11252 |
| rs146375588 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944762 | GGGTATAAGCAAAAA[A/T]GGCAGAGTGGCACAG | 11252 |
| rs146383299 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984169 | TAGAGACGGAGTTTC[G/T]CCATGTTGCTCAGGC | 11252 |
| rs146419425 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995322 | TATTCAATGCAAATA[G/T]TTAAAGAACAGGCTG | 11252 |
| rs146423938 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997935 | CTGAGTTCCACCCAC[A/G]TGTCTCAGAACACCA | 11252 |
| rs146437649 | in-del | -/GTAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886415 | AGCAATGGTATGTAT[-/GTAG]GTAGGTAGGTAGGTA | 11252 |
| rs146438713 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875902 | GGTCTCATACTCCTG[G/T]GCTCAAGCGATCCTT | 11252 |
| rs146504917 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880578 | GACACCCTGCATGGC[A/G]TATGGCACTCTATGA | 11252 |
| rs146507259 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956303 | AAGATTTATGTCTTA[C/T]GATTCATATATGACA | 11252 |
| rs146523785 | in-del | -/GTCA | 0.438666 | 0.164028 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941219 | CACGTTGCAGCATGT[-/GTCA]TGTATTTCACTCCTT | 11252 |
| rs146539631 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016309 | GTGGTTGTTTACTTT[C/T]TAGACTGCTCTGTGG | 11252 |
| rs146541420 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937358 | GGCACAGAAAGACAG[A/G]TGTGGCAGCAGTTCC | 11252 |
| rs146545747 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011637 | GGCAAGGACATCTGC[A/G]AGGCCGAGGCGGGCA | 11252 |
| rs146549502 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013171 | AGTCCCAAAGCAGCA[C/T]GAGCTAAGGATACCA | 11252 |
| rs146560829 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941663 | TGGGTATCTTTTCAT[A/G]TGCTTATTGGCCATT | 11252 |
| rs146560838 | in-del | -/ACACACATATGTATATATATGTATATATATATATATAC | 0.39121 | 0.2063 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990016 | CACACACATATATAT[lengthTooLong]ACACACATATGTGTG | 11252 |
| rs146586771 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010400 | CATATATATATATAT[A/T]TTTTTTTAATTGAAA | 11252 |
| rs146623401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898859 | ATCTCAACCATCCCT[A/G]TGCAGAAACATCCGT | 11252 |
| rs146626572 | in-del | -/C | 0.0737376 | 0.17729 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885758 | CTGCCCCTTTCTCCT[-/C]CTCCTGGTATCCGGG | 11252 |
| rs146662987 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956336 | GTCTAATAAGAAAAA[A/G]CTTAGGCCAGAGCCC | 11252 |
| rs146667025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960166 | AACTAACTTACACCA[C/T]ACATGAGTCTTCTAA | 11252 |
| rs146750402 | in-del | -/GGAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014396 | GGGACACGGAGGGTG[-/GGAA]GGAAGGAAATGGAGG | 11252 |
| rs146788796 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930102 | CCATGCTTTTCTCAT[C/T]GCGAACCATGAGGTG | 11252 |
| rs146788889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977702 | TTAGATCATGGAGGC[A/G]AATTTCCCCCTTGCT | 11252 |
| rs146854280 | in-del | -/TCAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978089 | CACTCACTCACTGGC[-/TCAT]TCATTCATTCATCCC | 11252 |
| rs146868509 | snp | A/C/T | 0.0138852 | 0.0822049 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936169 | TGCAGTGAGCCAAGA[A/C/T]TGCGCCACTGCACTC | 11252 |
| rs146870755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961096 | TCAACATGGCCCAAG[A/C]GGGTGTATGTAGGGA | 11252 |
| rs146908025 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964280 | AAAATTAGCTGGGCA[A/T]GGTGGCACATGCCTG | 11252 |
| rs146908426 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916981 | TTTTGGTGACGCTGC[C/T]ACCTGCCACTGTGAC | 11252 |
| rs146941587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974693 | GGTGGAGGTTGCAGT[A/G]AGTTGAGATTGTGCC | 11252 |
| rs146993180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942722 | TCAACTGACCATAAA[C/T]GTAGGGGTTTAGTTT | 11252 |
| rs146997649 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979988 | ATACACATACATGCT[C/T]AACTATATAAACCTA | 11252 |
| rs147013880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938221 | GTTTCCTGGGCTCGC[A/G]AAGCAGCAGAAGGTA | 11252 |
| rs147016004 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986282 | CACTGCGTCAGCCAC[A/G]ACGCTGGGCTGCAGT | 11252 |
| rs147096052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885552 | CTGCAGGCCTATCGG[G/T]CACCCTCTCTGCCCC | 11252 |
| rs147097655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960852 | TATGCATATTATTCA[A/G]TAACACTTTTTAAAA | 11252 |
| rs147104250 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999387 | AAAAAATCTGTCTAC[A/G]GGCCAGGCGTGGTGG | 11252 |
| rs147134661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934540 | GCAGCCTTGCCCCTC[A/G]TGGGCTGGCCCTGAT | 11252 |
| rs147135278 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009697 | CTCTGTCATCTCATA[A/T]TCTTGGGAGGAAAAA | 11252 |
| rs147151033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938612 | TCTGCACAGGCCAAC[C/T]GCATGTTCCGCAGGA | 11252 |
| rs147151318 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893288 | CCTTCTGGTGATGGG[C/T]GCTAATGCTCCCCAT | 11252 |
| rs147158370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006886 | AACACGTAAATGCAG[A/G]TTAAGAGAATGAGTC | 11252 |
| rs147207206 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897648 | TGGACATCCCTTCAC[C/T]CCCCTGAGGGACTGC | 11252 |
| rs147240195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955705 | CATGGCTTTACAGTC[G/T]TGCTTTCTAACATTC | 11252 |
| rs147255751 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958364 | CACCAAATGAATAAC[A/G]GAATTGTGTGGGTGG | 11252 |
| rs147256653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907805 | TAGCCCAGGGCCCGG[C/G]TCATGGCAGCTTCTA | 11252 |
| rs147263721 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951304 | GGACAGTCCTGCAAA[A/G]CACCCAATTGGTGCC | 11252 |
| rs147300496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010618 | GGGAGGCTGAGGCAG[A/G]AGAATGGCATGAACT | 11252 |
| rs147313028 | snp | A/C/T | 0.00199529 | 0.0315338 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912136 | GGGGTCAACTTCGAA[A/C/T]GCTCAAAATCTGTAG | 11252 |
| rs147346352 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970154 | CTGGCCTGAAGGGAT[C/T]AGCAATCTTTTGGGG | 11252 |
| rs147418394 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919623 | ACTAAAAATACAAAA[A/T]TTAGCTGGGTGTGGT | 11252 |
| rs147418554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934113 | TAAAAAGGAGCTTTG[A/G]AATTTTCTCTAATTT | 11252 |
| rs147453469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993578 | ACAATGGTCAAAATT[G/T]TATACAGAAAGAGCC | 11252 |
| rs147459930 | in-del | -/GA | 0.414905 | 0.187899 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871935 | CAACTTCCAGGCTGC[-/GA]GAGGGGAAGGGACCA | 11252 |
| rs147465600 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917521 | TCAGGAGGCTGAGGC[A/G]AGAGGATTGCTTGAG | 11252 |
| rs147465699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874666 | TCTCTCATGGCCCTG[C/T]GGGGCTAGCAGCTCC | 11252 |
| rs147489195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912518 | CTCCCCTCTCCAGAG[C/T]GGCTACCACATTCCA | 11252 |
| rs147534997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877929 | ACCAAGGAAGGGAGG[C/T]GAGGACATGCCTCCA | 11252 |
| rs147557254 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889992 | ACTGCACACGCAGAG[C/G]AGCCAAAGGGACTTT | 11252 |
| rs147577545 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885379 | ATGGTCGTGTTGTCC[C/T]CCTGGGGTGGGTGAG | 11252 |
| rs147577675 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927729 | AGTAGCTGGGATTAG[A/C]AGCATGCACCACCAC | 11252 |
| rs147612494 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943028 | TCCAGTCCATGGATG[C/T]AGGATCTCTTTCCAT | 11252 |
| rs147615912 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946853 | CACAAATACAGGAGA[C/T]ATGTGGACCATGTTG | 11252 |
| rs147649050 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986309 | CAGTGTGGTCAGCGA[A/G]TCTGGTAAGCACCCT | 11252 |
| rs147661894 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905114 | TGCACAAAAAAAATT[C/T]AAAAAATTTTATCTT | 11252 |
| rs147717694 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007096 | CTCTGAAGATCTTCA[A/T]CCCGGTATTTTAAAT | 11252 |
| rs147719493 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964156 | GGCACGGTGGCCCAT[A/G]CCTGTAATCCCAGTA | 11252 |
| rs147787327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894195 | GGCTTAGAGAAGTTA[C/T]GTGGTTTGTCAAGAT | 11252 |
| rs147821351 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979080 | ACAGACAACAGGGGT[A/G]CTACAAAGCTCCATT | 11252 |
| rs147908809 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870441 | CATTAAAACAGTAGA[C/T]GAGTGCTTTAGATTC | 11252 |
| rs147920922 | in-del | -/C | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924606 | CTCTCCAACCCGCCA[-/C]CCACTGCTGTCCACC | 11252 |
| rs147929676 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999305 | TCGAAGGGGTCCAGG[A/G]AACTCTCCCATTTCA | 11252 |
| rs147933223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003273 | AAAGAAAGCAAAAAA[A/G]AAGTCATTTGACACA | 11252 |
| rs147978598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901766 | AGCCTTCAGGATTCC[A/G]GGGTGTCTGGTTGAA | 11252 |
| rs148014533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943861 | CGTTAAACTTTTGCA[C/T]AATACAATATAGAAA | 11252 |
| rs148032156 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897332 | AAATATTTGACAAAT[C/T]GATCATACATTAAAA | 11252 |
| rs148034056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969553 | TGGCAACGATGACCA[C/T]TGTAACACCGGCATT | 11252 |
| rs148084271 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965483 | GAAAAGGAAGAAAAG[C/T]CCCCAGCAGAAGTCT | 11252 |
| rs148140617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916740 | GCAGGGACACACCAG[C/T]AGCTCTCAAGAGGCA | 11252 |
| rs148175677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989367 | GCTGGGTGTGGTGGT[A/G]GATGCCTGTAATCCC | 11252 |
| rs148192916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938793 | AAGTGCTCAAGTAAC[A/C]AGAGAAGACGACAAG | 11252 |
| rs148244030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933054 | CATTTATATTTACAG[C/T]AGAATTTGAAAACAC | 11252 |
| rs148246710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892245 | GGGGCAGAAATCGAG[A/G]AGATCCATGGCTGGT | 11252 |
| rs148298685 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003901 | CCCACGGCCTTGACC[A/G]CACCCCAGCAGCTCT | 11252 |
| rs148299914 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886102 | TCAGGGTACTCAGTG[G/T]CAACAAGATGCTCCA | 11252 |
| rs148300715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961141 | ATTGGCAAAAGAACA[C/T]ACTGCAAGGGGAAAC | 11252 |
| rs148304769 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993298 | GGTGGCCTGGAAGAA[A/G/T]TGGGGGCAGAGGGAC | 11252 |
| rs148353416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956884 | CAGAAGCTAGAGGCC[A/T]GGGAGGGAAGCATAT | 11252 |
| rs148391753 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006099 | CACTCAGCCACTCAT[A/G]CCTTTATAAAAAGTA | 11252 |
| rs148404887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889007 | TCCTGTGCATGGTTC[A/G]AGGCACCAGGAACAC | 11252 |
| rs148409190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963279 | TGGTTCTCCAAGAGT[A/G]TGCAACCAGCCTACT | 11252 |
| rs148432859 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014342 | ACACACACACACACA[-/G]CACACACACAGACAC | 11252 |
| rs148459426 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959032 | TTACATTTTGTTACC[C/T]GACAAAAATATAAAC | 11252 |
| rs148504119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997359 | GTCAGGAGATTGAGA[A/C]CATCCTGGCTAACAT | 11252 |
| rs148517295 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947676 | AAGACCCCTGGGGGT[-/G]GGGGGGGGGACCTCT | 11252 |
| rs148540703 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912556 | GAGCACTGTCCCCAC[G/T]CAACTCCACCTTTAC | 11252 |
| rs148546973 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017596 | CCTTATCCAGTTGCA[C/T]GAATCCCCCTGCACT | 11252 |
| rs148549628 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970988 | CTGCTACAGCCTACC[C/T]CTGCACCACCTCTCA | 11252 |
| rs148557867 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869303 | GGGCTGGCTGAGACT[A/C]CTCAAGAAACCCTGG | 11252 |
| rs148559060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898702 | ATGCCCTTCCCCGAG[A/C]CCAGGACTCGCCCTG | 11252 |
| rs148593220 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907692 | GCTCGCTTCGTGCTT[A/G]CGCTCAGGGCACTGC | 11252 |
| rs148597868 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012884 | GTCTCGAACTCCCGA[C/T]CTCTGGTGATCCGCC | 11252 |
| rs148598719 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967371 | GCCAACACAAGGCCG[C/T]CAACTTTATTTTGCC | 11252 |
| rs148615305 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923694 | GGCCTCCCAAAGTGC[C/T]GGCATTACAGGCGTG | 11252 |
| rs148668812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919112 | AAATCAATTTATTAA[C/T]GCAAAAAATATGTAA | 11252 |
| rs148704502 | in-del | -/AT | 0.0310518 | 0.120672 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985617 | AAACATTTGCAAAAC[-/AT]AAAGATAACAGGACA | 11252 |
| rs148752034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879964 | CTCACGAGTTCTCGG[A/G]TGGCGAACTGGCTTC | 11252 |
| rs148759986 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010645 | AACTCGGGAGGCGCA[A/G]CCTGCAGTGAGCCAA | 11252 |
| rs148774758 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894458 | ATGTTGGCCAGGATG[G/T]TCTCAATCTCCTGAC | 11252 |
| rs148789693 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874086 | TGAGCCATCGTGCCC[A/G]GACAAGATAACACTT | 11252 |
| rs148806735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950287 | TTTTATATCAGAGAC[A/G]AGCATCCATGGATTT | 11252 |
| rs148836957 | in-del | -/ATT | 0.0174175 | 0.0916809 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980019 | TGAAATAAGCGCATC[-/ATT]GTTTCCATTAAAACT | 11252 |
| rs148846555 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998859 | GTGGCAGAGGAGAGA[A/G]GAGAGGAAGTCGAGA | 11252 |
| rs148852012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986853 | TAAAAAAACCTTCCC[A/G]AAACCTAGATGTGGT | 11252 |
| rs148859275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881857 | ACAGGGTGGGTCAGG[A/G]ACCTGAGGTCCTGTG | 11252 |
| rs148862954 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956432 | GCAAATGCATTTAGA[A/C]CACCTAGTGAAATGT | 11252 |
| rs148865718 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938031 | TTGTACAGAGTAAAA[C/T]AAAATCATCATGTTA | 11252 |
| rs148879906 | in-del | -/GAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969545 | AATAACTCTGGCAAC[-/GAT]TGACCATTGTAACAC | 11252 |
| rs148920338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007593 | GGAGAGCACCTGTGG[C/G]TCTGGCACAATCCCT | 11252 |
| rs149001083 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964705 | CAGAGCCAGGTGATC[A/C]ATCGGCAGCAGGGAC | 11252 |
| rs149054262 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960653 | TTCCCTTTGGATCCA[C/G]CACAAGAAAAGGCGT | 11252 |
| rs149070354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915858 | ATACAAGGTCTCACT[C/G]AACTGTGCAGTCAGA | 11252 |
| rs149076136 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972326 | GCTCTTTAAGAGTCA[C/T]CACCACTCCCTAAGC | 11252 |
| rs149120347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910368 | AAGGGCCTGCACTTC[C/T]AAAGGCTGGAGAGCT | 11252 |
| rs149124827 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991607 | ATCCAATGATAGAGC[G/T]CCTGCTGTCAGGAGC | 11252 |
| rs149125783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941695 | GTATACTATCTTTGA[A/C]GAAACGTCGGTTTAG | 11252 |
| rs149158393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932094 | ATCCCGTCATGACCC[A/G]GCCCCTGCCTGCCCT | 11252 |
| rs149212757 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925415 | AACCTGGCAGGCAGA[A/G]GTTGCAGTGAGCCAA | 11252 |
| rs149213489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003682 | TCACAACGTTGACAA[A/C]ATGTGAAGACCTTTC | 11252 |
| rs149230027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885793 | TGCTCTGCTTCTCAG[C/T]CTCCTAAGATGGCTG | 11252 |
| rs149236431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943573 | TCCTGGTTTGCTGAG[A/T]GTTTCTGTCATGAAG | 11252 |
| rs149302878 | snp | G/T | 0.0322114 | 0.122752 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897151 | CGTGTTGCCTAGGCT[G/T]GTCTTGAATTCCTGG | 11252 |
| rs149319065 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927299 | TGCCCAGACTGGAGC[A/T]CAGTGGCACGATCTT | 11252 |
| rs149322964 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005382 | CAAGGCCTCTCTGCA[G/T]GGCAAGGCTGCCCTC | 11252 |
| rs149324326 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892127 | CTCACTGTTCTCAGT[-/C]CCCGAGGCTCAGGAA | 11252 |
| rs149374066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000738 | AAAAGAAATAAATCC[A/T]AAAGGAAATACAAGA | 11252 |
| rs149377219 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958736 | TAGGTAACATCCTAA[C/G]AAGAAAGCATGTTTT | 11252 |
| rs149389867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883686 | CCAGCCCAGAAATGC[C/T]AGATTCACCTCCAGT | 11252 |
| rs149395475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907008 | AGACTGCCCAAGCCC[A/G]CCCGGAGCAGTCAGG | 11252 |
| rs149411705 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012760 | TGGGTTCAAGCAATT[A/C]TCCTTCCTCAGCCTC | 11252 |
| rs149431816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953877 | GGAGGAAAAAAGAGA[C/T]GAAATTCACCTAAGG | 11252 |
| rs149446872 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904064 | AAAAAATAGATGACA[C/T]AGAAACCCAGAAATT | 11252 |
| rs149464427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009628 | CCTCAGGGTTGGTCA[A/G]GGAAAGGCTGGACAA | 11252 |
| rs149497437 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972512 | ATCAATAAATACTAA[-/AT]ATATATATATATATT | 11252 |
| rs149528156 | in-del | -/TTTTG | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941764 | TGCTGAGTTTGGGGT[-/TTTTG]TTTTGTTTTGTTTTG | 11252 |
| rs149534832 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967182 | TGTGAGAAGATGCCC[A/T]GGAAGGCTGGACTCT | 11252 |
| rs149584436 | snp | C/T | 0.029116 | 0.117091 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961680 | CAGGAGGCTGAGGCA[C/T]GAGAATCGCTTGACC | 11252 |
| rs149600377 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918651 | CCAACAAGACACCAC[A/G]TGCCCAGCTACCAGG | 11252 |
| rs149604212 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873845 | ATCACCCAGGCTGGA[C/G]TGCAGTGGTATGATC | 11252 |
| rs149622174 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976249 | TTCTCAAAATGCCTC[C/T]AGGCTTATCACTTTA | 11252 |
| rs149641109 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993059 | TAGTCCCAGCTACTC[A/G]GGAGCTGGGAGCTGG | 11252 |
| rs149653088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911674 | ACAGTAAAGTGCCTC[A/G]TAGGATAAGCTGAGC | 11252 |
| rs149658901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881426 | ATCTGAATGCAGCCC[A/G]GGCTCTGGCCGCTGC | 11252 |
| rs149690239 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934926 | CCTTTTTCTTTTTCT[G/T]TTTTTTTGAGACAGA | 11252 |
| rs149694712 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920045 | CCCAGGAGCTGGAGG[C/T]TGCAGTGAGCTACGA | 11252 |
| rs149712547 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875408 | AGGGTCTCGCTCTGT[C/T]GTCCAGGTTGGAGTA | 11252 |
| rs149727104 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951477 | GCTCCAGATCCGGCA[C/T]GGCCCGAGCTGCTGG | 11252 |
| rs149750335 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993954 | GAGCTGCTCACCCCC[A/T]AGCCACAGTATCTGT | 11252 |
| rs149757655 | snp | C/G/T | 0.0014399 | 0.0267935 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888796 | TTTCTTTGCTGCTTC[C/G/T]ACCTACAGGGAGAAT | 11252 |
| rs149764164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945325 | GCCTTCTCTCAACCT[C/T]CTCTGCCTGTTTCCT | 11252 |
| rs149839714 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007341 | CTGCCTCAGCCTCCC[A/G]AGTACCTGGGTTCAC | 11252 |
| rs149849770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902430 | GAGGGCAACTACTAT[G/T]CCTCTATATGTCTCC | 11252 |
| rs149892825 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003096 | CAGGACAGAGACAAC[A/G]TACCTCTCTTGCCTC | 11252 |
| rs149893267 | in-del | -/AATA | 0.0471551 | 0.14613 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997574 | AAAAAAACAATAAAT[-/AATA]AATAAATAAATAAAT | 11252 |
| rs149904895 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885232 | ACATGGCTAAAGTGG[C/G]CACATTCATCTGGTG | 11252 |
| rs149909123 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960470 | CAGCACGACTGTCTC[C/G]TAAGAACTAGGACAC | 11252 |
| rs149922876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910150 | CTGGCTCCAAAGCAA[C/T]GTCTTCACCTGTCCC | 11252 |
| rs149959725 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956153 | TGAAATTCATAGCAC[A/C]CTTCACATTAACAAA | 11252 |
| rs149976125 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905055 | TTATTCTGACATCAC[A/T]GAGATCAAATAAGAA | 11252 |
| rs149990184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984449 | CTTCCCTGATGTTGA[C/T]ATGTGAACCTAGTAA | 11252 |
| rs150044150 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007765 | ATACTGAGCTGCCTT[-/T]ACAGAGCAGCCATCA | 11252 |
| rs150049750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968390 | AGCATTCCAGGACGC[C/T]ACCATTATCTTCTCC | 11252 |
| rs150094614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906088 | GTGCTGAAAACTGTC[C/T]AAGGGAAATGGCAGT | 11252 |
| rs150099160 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986463 | CCACAACCCCTTCCC[A/G]GCATGGCAACCAGCA | 11252 |
| rs150149403 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979059 | CCAATCCCCCTGCAG[C/T]ATAGCACAGACAACA | 11252 |
| rs150186682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999914 | TGGCAGGCTCAGAGG[C/T]ACCGATGGCTGTGCT | 11252 |
| rs150218408 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937783 | GGCACCCATGCAGCT[C/T]CGAGAACAGCAAAGT | 11252 |
| rs150225179 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922364 | AGACAAAAGAACAGG[C/T]CATTTTTTAGGCCAA | 11252 |
| rs150256030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953672 | ATTGTCTTCATTTTA[C/T]AGCTGAAGAAACTAA | 11252 |
| rs150270975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929627 | CTTTTAGAATGGATG[A/T]CATACTAATCACACA | 11252 |
| rs150273590 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890657 | GAGGCACAGGTTGCA[A/G]TGAGCTGAGATTGCA | 11252 |
| rs150305731 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948229 | GGAGGGGAGAGGGGA[C/T]TGACAAATGGCAGGG | 11252 |
| rs150332887 | in-del | -/CAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876514 | CTCATCCTGAGCCAT[-/CAA]CAGGCTTTCCAGGGG | 11252 |
| rs150359932 | snp | A/G | 0.117886 | 0.21224 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014992 | CGCCCCAACCGTCGC[A/G]GCGACCCCTGACCTC | 11252 |
| rs150375214 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903803 | CAGCACTAGTCCTGT[A/C]CTTTCCTCGGGGCCT | 11252 |
| rs150384603 | in-del | -/CTGT | 0.039522 | 0.134904 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938872 | AGGTAAAAATGCTGT[-/CTGT]GACAAATTTGTATTT | 11252 |
| rs150428858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900242 | GTCCCCATGCCCTTC[A/G]GGTCACAGCTCGTCT | 11252 |
| rs150465506 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911562 | ACTGGCGGCAGATGC[G/T]CCAGCAAGTTTGAAG | 11252 |
| rs150489543 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957008 | AAAATATAATAGTAA[C/G]TATAAAATGCTAATT | 11252 |
| rs150523620 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901914 | CGGACCAGCTGGCTC[A/G]CCCCTGGCCCTTCCT | 11252 |
| rs150527117 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976091 | GGAGAACATTCATCA[A/T]CTTATTTTGCATGTA | 11252 |
| rs150563839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993880 | AAGAAGAATGTGGCC[C/T]AAAAGGTTCCTGAAG | 11252 |
| rs150572740 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913291 | TCAAGACCAGCCTGA[C/T]CAAGACGGAGAAACC | 11252 |
| rs150594137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926732 | AGCTCCTCAGGAGGC[C/T]GAGGTGGGAGGACTG | 11252 |
| rs150600735 | in-del | -/TCTCACCAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953364 | AAGAGAGAATAAAAA[-/TCTCACCAG]AAGAACTACAGCCAA | 11252 |
| rs150607813 | in-del | -/GT | 0.097727 | 0.198275 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949457 | GCCTCATACACACAC[-/GT]GCGCGCGCACGCACA | 11252 |
| rs150624800 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883499 | CTGGGACCTCTGCCC[C/T]GGTGAAGGCATCACA | 11252 |
| rs150627019 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989680 | GTGGGTGCCTGTAGT[C/T]CCAGCTACTTGGGAG | 11252 |
| rs150680900 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870165 | GTGCACAAGTAACAC[A/G]ACGACTGAAATCTGC | 11252 |
| rs150682296 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945196 | CAGTGACTAGATGTA[C/T]GCACCGGCAATTACC | 11252 |
| rs150734907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939147 | AGCTGGAGCTAACAG[C/T]GTGTAATTAGATGTG | 11252 |
| rs150751328 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898302 | TTTTGAGACAGTTTC[A/G]CTCTTGTTGTCCAGG | 11252 |
| rs150766894 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997550 | GCGACAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 11252 |
| rs150783183 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955766 | AGTGAACCTGAGGTG[A/G]CCGTCCCTATAGATG | 11252 |
| rs150788427 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008902 | GTACTCTTTCATCAA[C/T]AAGCATTAAATAAGT | 11252 |
| rs150801770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892679 | TGTGCTAAGCCCACA[A/C]AAACAACCCATGTCA | 11252 |
| rs150894529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904866 | TGCCTGGGCACCCCA[A/G]CTCCGCCCCCCTGCA | 11252 |
| rs150928048 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964044 | ATTTTCATTACCTCA[A/G]AGAGAAACCCTGTAC | 11252 |
| rs150931418 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952472 | CAAGCGATTCTCCTG[C/G]CTCAGCCTCCTGATT | 11252 |
| rs151000956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905691 | ATACACCAAAGGGCA[A/T]GAAAGAGCTGAAAAC | 11252 |
| rs151081597 | in-del | -/G | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990543 | GGCAAAACACCTGGA[-/G]GGGAGGGGAAGGTGA | 11252 |
| rs151109335 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971221 | CTGCCAAGCGCCTGG[A/G]ATTGCAGGCGCGCGC | 11252 |
| rs151136663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924402 | CTGTAGCTGTATGCA[C/T]TGCTGCATGCTTTCT | 11252 |
| rs151140872 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002686 | TAATACAAGATTTCT[A/G]TTCTCGGGAATTTAT | 11252 |
| rs151146297 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992053 | TTCTTCAAAAGATAC[G/T]GTTAAAAGAATGAAA | 11252 |
| rs151153761 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884631 | CACCCTGCCCCTGGA[A/G]TGTCTCAGGCCTTCC | 11252 |
| rs151206645 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950408 | AGATTAGGCTGAGAG[G/T]GAGGGAGGGAAGGGA | 11252 |
| rs151206964 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880414 | AATATAAATTCATCC[C/T]GATTGGGTGGCTTCC | 11252 |
| rs151213642 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871673 | TGACAGACCTAGAGA[C/T]GACAGTCTCACACAG | 11252 |
| rs151215238 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947884 | ACTGGGGCCAGGCTC[A/C]ACGGCAGCCCAGCTC | 11252 |
| rs151241804 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899642 | AGGCAGTCATTAAAT[C/T]ATAAAGCATGCAAGT | 11252 |
| rs151264919 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941954 | GCTAATTTTTGTATT[C/T]TTAGTAGAGACAGGG | 11252 |
| rs151281118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014203 | AAGGAGTTCGGATTT[C/T]TGATTCAGTGAGTCT | 11252 |
| rs151294929 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894812 | AATATGACAGAAAAA[C/T]GATCTCTTTTCAGCC | 11252 |
| rs151296272 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968191 | TGACACTGCAAGACA[G/T]CTGTGGGTGATTGCA | 11252 |
| rs151319051 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010790 | AAGAAAGACTCTATG[A/G]TGCTTTAAGTTTTAT | 11252 |
| rs180694337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886987 | CACAGGCACGCCCCC[A/G]CCCAACATGGAGAAG | 11252 |
| rs180703192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906356 | CAAAGTCTGTCCAAT[A/G]TTGACGTCTGTTTTC | 11252 |
| rs180943157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990468 | GAAGACAAACAGGTC[A/G]GTCATACCATACATG | 11252 |
| rs180946690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011557 | TAACCCCTTCAGAAT[C/T]AGTAAGCCTGAGCAT | 11252 |
| rs181011500 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936172 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 11252 |
| rs181021102 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972390 | CCGCAGGGTCCTCTG[C/T]CTAGGAAAACCAGAG | 11252 |
| rs181030246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929208 | TCACTGTGAAACAAG[C/T]CACAGTCAGCATAAA | 11252 |
| rs181044720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898264 | CCTTGGGAAAGAGAA[C/T]CTCCTTCCTTTTCTT | 11252 |
| rs181053791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919104 | GCCTTTGGAAATCAA[C/T]TTATTAATGCAAAAA | 11252 |
| rs181054370 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962947 | GACTATGGCAGAAGA[C/G]AAGACTGACTCAGGC | 11252 |
| rs181063138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944481 | TTGCTAATAGGCTTC[A/G]TGGAAAAATCTGAAA | 11252 |
| rs181064687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951247 | CTAGTCACGATAACC[A/G]GCCTGCAGTATTAAC | 11252 |
| rs181069398 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975078 | ACTTCTACTACATTG[G/T]AACAAGGGTGGCATT | 11252 |
| rs181069680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995498 | GAAGTTACTCTGTCC[A/T]TTGGGCAGGACCTTA | 11252 |
| rs181071537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979385 | AAAAATTAGCCAAGC[A/G]TGGTAGCAGGCGTCT | 11252 |
| rs181109905 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869595 | AAGGGAACCCCAAGG[A/G]GCTCAGGTGCCTCAA | 11252 |
| rs181143261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934466 | CACACCTTTCAATGT[A/G]GCAGCTGCACACAGA | 11252 |
| rs181147996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892457 | CTGTCCTGTCCACAA[C/T]GTTACAGCCAGACCC | 11252 |
| rs181148321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914095 | CTAACCAGGCTCTCA[A/T]GGAGAGAACTCCAGT | 11252 |
| rs181151587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958122 | CTCTTAGCTAAGTGA[C/T]ATTCATCTTAAGATA | 11252 |
| rs181164731 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968123 | TAGCGCGGGAAGCTG[C/T]AACCCTGGCTCCCTC | 11252 |
| rs181171372 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985289 | CCGAGATCTCATCAC[C/T]GCACTCCAGCACTCC | 11252 |
| rs181171955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007354 | CCGAGTACCTGGGTT[C/G]ACAGTCACAAACCAC | 11252 |
| rs181204326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953644 | GGGTTTCATTTAACA[C/T]GAGGAAAAAACCATT | 11252 |
| rs181206115 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880724 | ACAGGGGCTGGTTCC[C/T]AGCCCATGGACCCAC | 11252 |
| rs181212002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935979 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGAATCA | 11252 |
| rs181221331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924383 | TTCATACTTGTACAT[A/G]CAACTGTAGCTGTAT | 11252 |
| rs181223724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901971 | CAGTCTGCTGATGCC[A/C]CCAGCTGGCTGGCTC | 11252 |
| rs181233895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939993 | AATGAAGGAAAATTC[C/T]ACCTAGCACCAGACA | 11252 |
| rs181259997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896246 | GATGGCAAGGATATA[C/T]GGAATACACAGTATG | 11252 |
| rs181268189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874079 | ACAGGTGTGAGCCAT[C/T]GTGCCCGGACAAGAT | 11252 |
| rs181272597 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918235 | GTCCAAGGAGCTAGA[A/G]GAGCTGCCTCATGGC | 11252 |
| rs181282289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908084 | ATGTTCTCTTCATCT[C/T]CCCAAATACTCTTCT | 11252 |
| rs181289224 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972177 | GAAAGATTCTTCTGC[C/T]TTGGGACGCTGTTGA | 11252 |
| rs181309390 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946179 | ATAAGAATCCTTCCA[A/G]TTACTTTTATAACAT | 11252 |
| rs181309470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011332 | ATGTGGTCATTAATC[A/G]CATAATCTACAGGGC | 11252 |
| rs181319574 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980133 | TATGGCAAAACAAGT[A/G]TAGAGTATTGGGTGA | 11252 |
| rs181380455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888472 | GTGGCTATGGTGAGG[C/T]GAGGTGCTAGGGCAC | 11252 |
| rs181389486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930269 | GAGGGTCTCTGTGAC[A/G]TGCAGCCTAACTCAC | 11252 |
| rs181395698 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990001 | ATATATACATATATA[A/C]ACACACATATATATA | 11252 |
| rs181398303 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964709 | GCCAGGTGATCCATC[A/G]GCAGCAGGGACGACA | 11252 |
| rs181556963 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003672 | TTATGTGATATCACA[A/T]CGTTGACAAAATGTG | 11252 |
| rs181630482 | snp | A/G | | | downstream-variant-500B | PACSIN2 | GRCh38.p7 | 22:42869270 | GGGTGGTTCCTCAGG[A/G]ATTTCGCTCAGTGCT | 11252 |
| rs181681173 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007031 | AATTGAGTCACCTGA[A/C]TCACCCCTCCCCCAT | 11252 |
| rs181684410 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976329 | AAGGCCAGAAGCTAC[A/G]CCCTGGTGAAAGGCC | 11252 |
| rs181685691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959638 | AATAATGAACTAATT[G/T]AACATTGCCGTCACG | 11252 |
| rs181696763 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997824 | AGGTGGAGGATGCAG[C/T]GAGCTGAGATCACAC | 11252 |
| rs181741655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926657 | ATGACAGACCAAGCC[C/T]TCTTCTTCCCACAGG | 11252 |
| rs181756029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941162 | CTCTGGTGATTGGCT[C/T]CCTTCACTTTTTCCA | 11252 |
| rs181820379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963815 | TATTTGGCAAAAGGT[C/T]GTGTCATTTGGAAAC | 11252 |
| rs181823666 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002310 | CTGTGAGATACCTAC[A/C/T]GCGATGGCTGAGCTG | 11252 |
| rs181847586 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887367 | CTCTCACCTGCTGGA[C/T]GGCACGTGACTTAAC | 11252 |
| rs181876545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906775 | CTCCCCAAAATAAGC[A/G]TAAGAACCTTAAACG | 11252 |
| rs181879995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945151 | TATCCCCAGTGCTTA[A/G]CATGAGGTAGATGCT | 11252 |
| rs181882565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892179 | CATTTCTATTCAGGG[A/G]GTAGGGTGGGGTGGC | 11252 |
| rs181883924 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933535 | GGGTGGTCTGTTAGA[C/T]GTCTAGACCAAAATG | 11252 |
| rs181887583 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929654 | CACAGCTGGGGACAT[C/G]TTTCCAATTGTGTGA | 11252 |
| rs181911284 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967761 | GGCGTGGGGGTGGGC[A/G]CCTGTAGTCCCAGCT | 11252 |
| rs181979441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881685 | ATGATGGGAAAAGAA[A/G]AACATTCATTTTGAA | 11252 |
| rs181981291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912425 | TGGGCTTGCCCATCC[C/T]GACCTACTCTACCTA | 11252 |
| rs181990223 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902592 | CAAACAACTCATGAT[C/T]CTTTATCTGTCAGTT | 11252 |
| rs181990612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991175 | GAAGCTGCTGTACAA[C/T]GGTATAGACTTGGAG | 11252 |
| rs181996989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933348 | AGGGCGGGCAAAGCC[A/G]ACTTCACCAGTGACT | 11252 |
| rs182106958 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015915 | CCAGGTAACTTGCTG[G/T]GGGTGATGTGGAGTA | 11252 |
| rs182131391 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913309 | AGACGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 11252 |
| rs182147937 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940630 | ACCCCAGGTCCTGGG[A/T]TTCCCTATACCCAGC | 11252 |
| rs182151801 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975564 | TTTTATAAAATTCAT[A/C]AACAAAAATAGAATA | 11252 |
| rs182161696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986345 | TTTGGAAAAGCGCAG[A/C]GGCCCCCAAAGAAAA | 11252 |
| rs182169205 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015549 | TTCAGAAAGTTTCCT[C/T]TCCCAAGGGACTCAA | 11252 |
| rs182179466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008006 | TGCCCCAGCTGGCTG[A/C]AACTCTATCAATAGT | 11252 |
| rs182181618 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950309 | CATGGATTTTGGTAT[A/C]CTTTGGAGGGTCCTG | 11252 |
| rs182273718 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973054 | CGGAAGTAAGAACTT[C/T]GACAGGGCAGTCATA | 11252 |
| rs182280389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011943 | CAAGGTCAGGAAATC[A/G]AGACCATACTGGCCA | 11252 |
| rs182346403 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012838 | TTTGTATTTTTAGTA[A/G]ACATGGGGTTTCTCC | 11252 |
| rs182354342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931092 | CATGCCTATTCCAGA[C/T]GCCTGCCTGCTCAAA | 11252 |
| rs182358695 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889195 | GACATGGAACACGCA[A/C]ATGGAGCACGCACAT | 11252 |
| rs182364888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909923 | GACTCCCTCAGCTCC[C/T]GTGTCAGAGGGAAGG | 11252 |
| rs182404047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926348 | CTGGGCAGGGTGGGG[C/T]AGAACACACTCAAAG | 11252 |
| rs182410032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959299 | AAAGAAAGAAAATGG[A/C]AGCATGTAATAAACA | 11252 |
| rs182418284 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955896 | CAGAGAAGATAGAGA[A/C]GTCATTTCATTATCC | 11252 |
| rs182426506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973769 | CCATCCTCCACTCCC[A/G]TCTCCATCATCCCTC | 11252 |
| rs182426699 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992884 | AAGAATATATACTGG[C/T]CGGAAGTGGTGGCTC | 11252 |
| rs182432870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996860 | CCTAGGTATGAGGCC[C/T]AGGCCCAGCTTTCTC | 11252 |
| rs182447597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891547 | CTGGGATTACAGGTG[C/T]CCGCCACCACGCCTG | 11252 |
| rs182493767 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971275 | ATTTTTTGGTGGAGA[C/T]GGGGTTTCGCCGTGT | 11252 |
| rs182498480 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998234 | CAGAGAACCTGGGGA[C/T]CCAGCAAAATTCCTT | 11252 |
| rs182503842 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016376 | AGAACCGGCTAGGCA[C/T]GGTGGCTCACGCCTG | 11252 |
| rs182537367 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942289 | GATATATGATTTGAA[A/T]CTATTTTCTTCCATT | 11252 |
| rs182546520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977359 | CAGTAGACGGAAAAA[C/T]GGAGAAAGGATATAG | 11252 |
| rs182553947 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894366 | CTGCCTCAGCCTCCT[C/T]AGTAGCTGGGACTAC | 11252 |
| rs182565185 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017042 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11252 |
| rs182567715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915817 | CACAATCAACTACTT[C/T]CATCTGAACCCTCTA | 11252 |
| rs182575726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977254 | TAAAAACAAACTATA[A/G]AAACAATAGCTGGGG | 11252 |
| rs182577540 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952503 | AGCTGGGACTTTAGG[C/T]GCGCACCACCACGCC | 11252 |
| rs182581478 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935048 | AGCCTCCTGAGTAGC[C/T]AGGACTACAGGTGCC | 11252 |
| rs182676143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900843 | CATGGTCATGCAACA[G/T]AAAGAGAGGCCACCT | 11252 |
| rs182680442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876759 | GGCCAGGGTGCGGCA[C/T]GCCAGGTGCCCACTT | 11252 |
| rs182681326 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938361 | CCTGAAGAAGAAAGG[A/G]AAGCCCCTGATGCAG | 11252 |
| rs182689791 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899714 | CCATAGAAGTGTTCC[C/T]TTTGGTCCCAGGACA | 11252 |
| rs182690916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965818 | TTCAATGGCTGCTAG[A/G]CAGTAAACCAGTAAA | 11252 |
| rs182705580 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004244 | GATGGATCAAGTGGA[A/C/G]AGAACACTATCTGGT | 11252 |
| rs182705976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920614 | GAAACAAGGCCGCAC[C/T]GCCCATGGTGGAGGA | 11252 |
| rs182719642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937978 | GCCTGCCTGGTTGAT[A/T]TTTCCCAGCTAACTT | 11252 |
| rs182790614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987762 | GATGGTCTCAATCTC[C/T]TGACCTCATCATCTA | 11252 |
| rs182817801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960667 | AGCACAAGAAAAGGC[A/G]TAACTAATCTACACC | 11252 |
| rs182828266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998871 | AGAAGAGAGGAAGTC[A/G]AGAGGAGTTGAGCTG | 11252 |
| rs182840681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926915 | CAGTGCAGTTCTTCT[C/G]CTTACCACACCTGGC | 11252 |
| rs182843506 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959763 | TTCAAAGAGGTCTAC[C/T]TTAAAGGAAATGCAA | 11252 |
| rs182919779 | snp | G/T | | | missense | PACSIN2 | GRCh38.p7 | 22:42884537 | GGTCGAGTTCCTTCA[G/T]GGACTTCTCATACTT | 11252 |
| rs182940607 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017434 | ACTCCTGGGCTCAAG[C/G]AATCCTCCTGCCTCA | 11252 |
| rs182958596 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947678 | GACCCCTGGGGGTGG[C/G]GGGGGGGACCTCTTA | 11252 |
| rs182968645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980430 | ACACTCCAGCCTGGG[C/T]GACAGAGAGAGACCC | 11252 |
| rs182971028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921781 | TGCTTTGTCATTGCC[A/C]AGGCTGGAGTGCAGT | 11252 |
| rs182993805 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973308 | CACAGGTCTCGCCCA[A/C]AAGGCAATCCCTCCT | 11252 |
| rs182998175 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955631 | TCAATTTAATGTCTT[C/T]GAGTTCAATGTGAAG | 11252 |
| rs183030456 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878405 | GCCCCCGTATGAAAT[C/G]ACTATTACTGAGTGT | 11252 |
| rs183064654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983038 | ATACAAAAATTAGGC[C/T]GGGCACAGTGGCTTA | 11252 |
| rs183067962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004588 | GTTCCTCTGAAGACC[A/G]CAATTCATGATCTTG | 11252 |
| rs183083359 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010118 | GAAGTGATCTGCTCC[C/T]TTACTTCCCATAGTG | 11252 |
| rs183126403 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903189 | GCTAGAGGGGGCTCC[A/C/T]GGACTGAGTCCCTTC | 11252 |
| rs183128152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911150 | ACCTCAAGATCCACC[C/T]GCCTCGGCCTCCCAA | 11252 |
| rs183135494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948407 | ACACCCATCAGAAGC[A/G]CTATCTAGAAGTGAA | 11252 |
| rs183139756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941750 | GTGTGTCTTCTTATT[C/G]CTGAGTTTGGGGTTT | 11252 |
| rs183143361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931476 | AGGCAGGAGGTGTCC[A/G]AGACAGAAGAGACCT | 11252 |
| rs183143806 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966500 | GTATCAGTTCTATCT[C/T]TGGCAAAGGAGAAAA | 11252 |
| rs183173519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883733 | AGCTGCGGCCAGGTG[C/T]GGTGGCTCACGCCTG | 11252 |
| rs183195986 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902903 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCTATTT | 11252 |
| rs183267372 | snp | C/G/T | 0.00518157 | 0.0506848 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904199 | GCCGTCGGCCAGGCT[C/G/T]CCCATGCTCTGCTCC | 11252 |
| rs183272676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934656 | ATCTCCTCCAAGAAG[C/T]CCCCCACCGTTCTAG | 11252 |
| rs183277569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884795 | CAGACAGGTAGATGC[C/T]GGCAAAGGGCAGTCT | 11252 |
| rs183278780 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969068 | CCATCCATCCATCCA[C/T]CCACCCTATTGGCTC | 11252 |
| rs183278833 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927807 | GGTCAGGCTGGTCTC[A/G]AATTCCAGACCTCAG | 11252 |
| rs183281639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951599 | CAGGACACAGCTGCT[C/T]AGGACAAATGCCCCA | 11252 |
| rs183325630 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875973 | CCACCACATCCAGCC[A/C]ATTGGCTGCTTTTGA | 11252 |
| rs183407949 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948807 | CTGTAGAGAAGAATA[C/T]GGAGCCAGTTTCGTG | 11252 |
| rs183414078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012441 | CTGCAGAATGCTATG[C/T]TGGTGGAAATCCAGA | 11252 |
| rs183421113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983174 | ATACAAAAATTAGCC[A/G]GCTGTGGTGACGCAC | 11252 |
| rs183536763 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934984 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 11252 |
| rs183573438 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969992 | ATGGCCAATCCTGTT[A/T]CACCTGTGATGTGAA | 11252 |
| rs183586899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009220 | GGACGGCCTCTGGCT[A/G]TTTGCTCCATCAACG | 11252 |
| rs183595431 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996232 | CTCAAAAAAAAAATA[A/T]TAAAATTAGCCAGGT | 11252 |
| rs183622177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893208 | GTGCAAGTGTGTCCT[A/G]TGGATGACAAGGGCT | 11252 |
| rs183628683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992048 | TTCTGTTCTTCAAAA[A/G]ATACTGTTAAAAGAA | 11252 |
| rs183633303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967031 | TAACTTAAACGAACT[C/T]GTCCGTAAGCAGCTT | 11252 |
| rs183661244 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005161 | TATCTTAATACAATT[C/T]CACACAGGTGAGCAG | 11252 |
| rs183689589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996193 | CCACTGCACTCCAGG[C/T]TGGGCGACAGAGCGA | 11252 |
| rs183693668 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010579 | GCCAAGTGTGGCGGC[A/G]GGCGCCTGTAGTCCC | 11252 |
| rs183698112 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919976 | AGCCAGGGGTGGTGG[C/T]ACACACCTGTAGTCC | 11252 |
| rs183705001 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955300 | GAATGAATGAATGAA[C/T]AAACAAACGAACGAA | 11252 |
| rs183708439 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015305 | GGACGAGGGAAAGCC[C/T]CAGGACGCGCATTGG | 11252 |
| rs183714063 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889692 | ATCTACCGTCTACTC[C/T]ATTCCAGCTAGGAAT | 11252 |
| rs183742257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887140 | CCAGGCTCCTCACCT[A/G]ATCCCACCGTGGAGG | 11252 |
| rs183760904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929274 | TAAATTACTTACAAT[A/G]TTGGTAACACAAGGT | 11252 |
| rs183763921 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971857 | GGAGGTGGGGGGCAG[A/C]CCCCGCCCAGCCAGC | 11252 |
| rs183765623 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952743 | TCTCGGCTCACTACA[A/G]TCTCTGCCTCCCAGG | 11252 |
| rs183769865 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906433 | ACCACCCATTTAAAA[A/C]CACGTAATTCTGAAG | 11252 |
| rs183774258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944592 | TCAAAGAAAAAATAG[C/T]TTGGACAAAATGTTC | 11252 |
| rs183774918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988662 | GCTCTCTGTACCAAA[C/T]GCAGTTCAGTTAACA | 11252 |
| rs183779264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915250 | AGTAAGAGCCTGAAT[C/T]ACTGAGGAGAGAGGT | 11252 |
| rs183787177 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952164 | ACCAGGATTTTGCCT[C/T]GTTTGCCCGTGTTCC | 11252 |
| rs183799955 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986618 | AGATACACACTAAAA[A/T]CCACATGGGAACACA | 11252 |
| rs183838621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999860 | AGCCTATTTCCTCAA[C/G]TGTAAAGTGGGAATC | 11252 |
| rs183890188 | snp | A/C/T | 1.65622e-05 | 0.00287764 | missense | PACSIN2 | GRCh38.p7 | 22:42891102 | TCAGTGAGGCCTTCA[A/C/T]CTCGAGGTGCAGCTC | 11252 |
| rs183903873 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914978 | AAGCAATCCTCTCGC[A/C]TCAGCCTCCTGAGTA | 11252 |
| rs183904078 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870222 | TACAGTGTTCTGCTA[C/T]GGAGCCAGGACAAAG | 11252 |
| rs183907499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937449 | TAAACGGGCACCGAA[A/G]ACAAAACAAAATGAC | 11252 |
| rs183911701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933176 | ATCCCTGAAAAGTTG[A/G]GGTCTAAGACTTTAA | 11252 |
| rs183917091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912337 | GGGCACATATGTGTA[C/T]GTCTGTGTGTGTGCA | 11252 |
| rs183920756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949854 | ACTGAGTAAATATCA[A/G]GCCAAGGAAATTGAT | 11252 |
| rs184001853 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898994 | CCTGCATGCATCTGT[C/T]GTAAACAGTCCAGAG | 11252 |
| rs184014453 | snp | A/C | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871795 | TGGCCAGGTGGCAGG[A/C]ATCGTCCCTCGGTTG | 11252 |
| rs184071583 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893153 | CGGCAAGGCCTTCCA[C/T]GTGATAGGAACTTAC | 11252 |
| rs184122363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990159 | TTTTTAAAAAGAATG[A/G]TTTTTAAACACAGCT | 11252 |
| rs184222785 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979406 | GCAGGCGTCTGTAAT[C/G]CCAGCTACTCCAAAG | 11252 |
| rs184261002 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994361 | CCAGAAAATAAGCAT[C/G]AACTTTACCATTCAA | 11252 |
| rs184261106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014069 | GAAAAGAAAATCGAC[C/G]TTCTCTGATGGAGCC | 11252 |
| rs184299549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917099 | CCATGCACTACACGC[A/G]TGCACTCCATTTAGT | 11252 |
| rs184301820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923413 | ACTTCATCTTCAACT[A/G]TTTCTCCTTCTTCTT | 11252 |
| rs184304999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880159 | ACGGCTCTGCTCACA[C/T]GTACTTACAGAACTT | 11252 |
| rs184309509 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901671 | GCTCTCCGCCTGCCA[C/T]GGCGATCGCCTGACA | 11252 |
| rs184313520 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939639 | TTCAAAGTTGGGTGG[G/T]ACTAGAACACACAAT | 11252 |
| rs184327310 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974794 | AAGAAGGAGGAGGAG[C/G]AGGAGGAGAGGAAGA | 11252 |
| rs184329218 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957839 | TTGTATTAAGTTTGG[C/G]ATTCTCATCTGGCAA | 11252 |
| rs184365103 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962951 | ATGGCAGAAGACAAG[A/C]CTGACTCAGGCAGCT | 11252 |
| rs184384710 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977758 | CGGAGATCTGAAGCA[C/T]GTGGCACTTCCCCCC | 11252 |
| rs184386232 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999407 | AGGCGTGGTGGCTCA[C/T]GCCTCTAATCCCAGC | 11252 |
| rs184389350 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000329 | GGACTGGTAATTTGC[C/G]AACTCTACCCCAAGG | 11252 |
| rs184407937 | snp | C/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967413 | TTTAAAAAAGAAAAA[C/G]ACCTATCACTCCCAT | 11252 |
| rs184417062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005996 | TAGGGTCTCACTATG[C/T]TACCCAGGCTGGCCA | 11252 |
| rs184431470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975244 | TTTAGTACTTTCACA[A/G]GATACAGAAATCCAT | 11252 |
| rs184431983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895674 | AGGAAGAGTGTTTCC[A/G]TAAGTACACATTTCA | 11252 |
| rs184432438 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873346 | GATATCAGAAACTGG[A/G]TGAAGATGGCTTAAA | 11252 |
| rs184437835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935214 | ATAGGCGTGAGCCAC[C/T]GTGCCCAGCCCAGGG | 11252 |
| rs184438736 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927882 | GTGAGCCACCGTGCC[C/T]GGCCTCAGTCATTTT | 11252 |
| rs184444045 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905054 | GTTATTCTGACATCA[C/T]TGAGATCAAATAAGA | 11252 |
| rs184446998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943400 | TGTCTAACTTCGAAG[C/T]TCCTGGTTAGACTCT | 11252 |
| rs184451407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896087 | GATCTGAATGTGGAC[A/C]AACATATACCACTGT | 11252 |
| rs184465746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962025 | GTGCCACGCCCGCCA[C/G]AGCTGGCAAGCACTC | 11252 |
| rs184538407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958323 | TTACAGCTCTAAATA[C/T]TGCGTTCCCACCTTC | 11252 |
| rs184542312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983436 | CGGAGGTTGCAGTGA[C/G]CCGAGATTGTGCCAC | 11252 |
| rs184557613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928455 | CATGCATCAGAGTAC[A/G]GAAATCAGGTTGGTT | 11252 |
| rs184565904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962715 | AGCCTGGATGCCTGG[A/G]GTGGGTGGAGGCATT | 11252 |
| rs184590354 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901411 | GGGCAAAATGCTTTC[A/C/G]ATAACTTGTTCAAAT | 11252 |
| rs184598493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879304 | CAGGGCCCCAGCTCT[C/G]CCTGGTTTCCCAGAA | 11252 |
| rs184646424 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885770 | TCCTCTCCTGGTATC[C/G]GGGTCCTTGCTCTGC | 11252 |
| rs184703605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944241 | ATCCTACAAGGGACA[C/G]ACAGATCAAGCGAGA | 11252 |
| rs184707845 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979281 | GCAATCTCAGCACTT[C/T]GGGAGGCAGAGGCAG | 11252 |
| rs184744623 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967721 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 11252 |
| rs184754849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984159 | TGTTTTTTTGTAGAG[A/C]CGGAGTTTCGCCATG | 11252 |
| rs184782723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905655 | CTGAGCACGCAGGCC[A/G]AAGACAATGTTGTAG | 11252 |
| rs184814007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912238 | TATTTCACAACTTCC[C/T]GTTTCTAATCACTGC | 11252 |
| rs184911923 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890289 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCAAGGAC | 11252 |
| rs185014375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972551 | ACCACCATTTTAGAA[A/G]AATAGTTCCTTATAC | 11252 |
| rs185014397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990673 | AGGAGTGTGGCAAGA[A/G]ATGAGACTCAACGGG | 11252 |
| rs185022290 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011606 | CAGACTTTCAAGGTA[C/T]AGAGAAGAAACAAAA | 11252 |
| rs185028665 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966126 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 11252 |
| rs185050133 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011341 | TTAATCGCATAATCT[A/G]CAGGGCGGCCTCCAC | 11252 |
| rs185068797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006676 | AAAAATTAGCCCGGC[A/C]TGATGGCGCATGCCT | 11252 |
| rs185082341 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985469 | TTGTGGCCCCCCACT[C/G]GCCTCACTTCTCTCC | 11252 |
| rs185140581 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870195 | CAACTACTGCAAAGA[C/T]GCGGGCACTTTTACA | 11252 |
| rs185145620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914257 | TTTTTTTTTTAGGTG[A/G]AATCTGGCTCTGTTG | 11252 |
| rs185147696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892480 | CCAGACCCACAAGGT[A/G]AGGGTGGTAAGGGTG | 11252 |
| rs185158751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951280 | CATTCTCTCTAGACA[A/G]GTAATTCCGGACAGT | 11252 |
| rs185162424 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934505 | TGGGGCCTCCCCACT[C/G]TGGCTTCCCAGCCTG | 11252 |
| rs185164085 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968612 | TTGGGGTGTGTCCAT[G/T]GGGCTGTTTCCAGAA | 11252 |
| rs185237895 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932067 | AACCCTAACTCCTCC[A/G]CTGTACTGCAAATCC | 11252 |
| rs185242716 | snp | C/T | 0.030665 | 0.119967 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971956 | TCTGCCCGGCCGCCC[C/T]GTCTGGGAGGTGAGG | 11252 |
| rs185269617 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896968 | TTGAGACAGGGTCTT[G/T]CTTTGTTGCCCAGGC | 11252 |
| rs185282751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874446 | TTTATAAAACTATGG[C/T]TTCTGCTCCTAGCAA | 11252 |
| rs185284523 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918512 | ATAAAAGATGTATTA[C/T]TGTTTCCATTTGATG | 11252 |
| rs185300755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936072 | ATACAAAAAATTAGC[C/T]GAACATGGTGGCGGG | 11252 |
| rs185307690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935952 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 11252 |
| rs185310075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972211 | ATGGCCTTGCCCCCA[A/G]TCCCGTGCTCTCTGA | 11252 |
| rs185314898 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953661 | AGGAAAAAACCATTG[C/T]CTTCATTTTATAGCT | 11252 |
| rs185336724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953189 | TTTTCTATCCTTCCA[C/T]TGTTCAAGAGAAGGG | 11252 |
| rs185364005 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989649 | AAAATACAAAAAAAA[A/T]TAGCTGGGCATGGTG | 11252 |
| rs185372886 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956248 | TCCTATTAGATTCTT[G/T]AAGTTTCTCAAAATA | 11252 |
| rs185394552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993709 | TGAGACTGGCAGGAA[C/T]GCCCCTGAAGGCCGA | 11252 |
| rs185406047 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885453 | CTATGGGGGTAGTCA[C/T]GGGCTCCACTCAGGT | 11252 |
| rs185436493 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918183 | GCCACTGCAGACAGG[C/T]CACACCCTAGAATAG | 11252 |
| rs185444047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891717 | GGCCATGCCTTTCCT[G/T]TATTTAAAGCCACTG | 11252 |
| rs185452917 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922706 | AGGGCCCTTTGATAA[A/G]GGACATATTTACCAT | 11252 |
| rs185488945 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912468 | AGGACCCGGGATAAA[A/G]CGTGAGTGGAGGTAA | 11252 |
| rs185497202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939089 | GGTCACCCGTCCCAG[C/T]GCAGCCCATCAGCTC | 11252 |
| rs185500458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974618 | GCTGGGCATGGTGGT[A/G]TGTGCCTGTAATCCC | 11252 |
| rs185521284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013039 | TCAGGTGATCTGCCC[A/G]CCTCGGCCTTCCCAA | 11252 |
| rs185584137 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872608 | CTTCCAGTGCTCCCC[A/G]GACTGCCTGGGCTCA | 11252 |
| rs185809912 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982845 | CCAAATCCCCCTCTG[C/T]GAGAAACACCAAAGA | 11252 |
| rs185824605 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869347 | CCTCTGTTTCCTCCT[C/T]GGTAGAATGGAAATG | 11252 |
| rs185875890 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954773 | AAAACAGACAGGACA[C/T]AGTGATGGATGATGC | 11252 |
| rs185945154 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919672 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATC | 11252 |
| rs185946307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004272 | GGTTGCAAGAATTAA[A/G]TGGGCAGGAATGTAA | 11252 |
| rs185949340 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875301 | GTATGCAACACCACG[A/C]CCAGCTAATCTGCTA | 11252 |
| rs185949924 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016013 | GACTGTGTAGCACTA[C/T]GGGAAAATGCTTAAA | 11252 |
| rs185964376 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007719 | TCTGGTACCGCCACA[A/G]TGAAAAGAGAAGTTT | 11252 |
| rs185988977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936838 | ATCACCTGAACCCGC[A/G]AGACGGAGGTTGCAG | 11252 |
| rs185997805 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926706 | CTGGAGCTGAGTGCA[C/T]CTGTGGTCCCAGCTC | 11252 |
| rs186004724 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902909 | GTGAGCCACCGCGCC[A/C]GGCCTATTTATCAGT | 11252 |
| rs186008961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941208 | TCAAGGTTCGTCCAC[A/G]TTGCAGCATGTGTAT | 11252 |
| rs186038829 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976357 | GCCACTGGCAAGCGC[A/G]GGCCTTAATGCACAC | 11252 |
| rs186040939 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998029 | TCCTGGAAAAGAGGT[G/T]TCTCAGGAGCCAGCC | 11252 |
| rs186080829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898701 | CATGCCCTTCCCCGA[G/T]CCCAGGACTCGCCCT | 11252 |
| rs186096347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902266 | GCTCTGAGGCAAGGC[C/T]GCTTTCTCACAGCTG | 11252 |
| rs186145894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924425 | TGCTTTCTCAATGCA[C/T]GATATATTTAACAAT | 11252 |
| rs186159546 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899360 | GGTGCCATCTCGGCT[A/C]ACTTGCAACCTCTGC | 11252 |
| rs186161323 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945552 | TCCTGGGTTTTCTAC[A/G]TCAGAAATGGTCCCA | 11252 |
| rs186167600 | snp | A/G | 0.00201983 | 0.0317149 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876285 | GTTGTTAGACTCATC[A/G]TCTGACCAGTCGGTG | 11252 |
| rs186167743 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929655 | ACAGCTGGGGACATC[C/T]TTCCAATTGTGTGAC | 11252 |
| rs186169723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964100 | CAACCCTTTCCCCAG[A/C]CCGCGGCAGTCATTG | 11252 |
| rs186176818 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920555 | CTCCTTCTCCTTCCT[C/T]CCAAAGGCCTGCTGA | 11252 |
| rs186181880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979888 | CTGCAAACCCCTGCT[C/T]ATGCCAACTGTACTT | 11252 |
| rs186185795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002540 | ATCTCACAGATACTT[A/G]GAAGTTCTAAAGGCC | 11252 |
| rs186192449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888496 | AGGGCACTCACCTGT[C/G]GCCTTCTTGAGGACA | 11252 |
| rs186194253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930497 | GTACATGGATACCCA[C/G]GTTCACACCACATAA | 11252 |
| rs186232168 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881297 | CATGTTCCCTAACAG[C/T]CCCCGACAGGAGATG | 11252 |
| rs186286847 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881756 | CCTTTGTTGGAAGGG[C/T]AGGGAGGGCTGCCCA | 11252 |
| rs186291538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902767 | TACAGACATGCACCA[C/T]CACGCCTGGCTAATT | 11252 |
| rs186330983 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908722 | CCTTAGCTCCAAAAA[C/G]GTCAAGGTCCTCAGC | 11252 |
| rs186429743 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969736 | TCGAGTCCACGTGTT[C/T]GAGACCAGCCTGGGC | 11252 |
| rs186444076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986346 | TTGGAAAAGCGCAGC[A/G]GCCCCCAAAGAAAAC | 11252 |
| rs186446219 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008454 | TGGGGTTTCACCATA[C/T]TGGCCAGGCTGGTCT | 11252 |
| rs186507755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964792 | AGGAATTTGTAACTC[C/T]CCATCTCCAGAAAGG | 11252 |
| rs186519534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003733 | CCTCTACAGAAACAC[A/C]ATTTCTTCTCCCTTG | 11252 |
| rs186582402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931223 | GATATGTGAGAAGCA[G/T]CAATGAATGAATCCC | 11252 |
| rs186589620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910275 | GGTGCCAGCCAGCAA[A/T]GTCACTACAGTTACA | 11252 |
| rs186654690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950805 | GCAGCCTTACTTACC[A/G]TATGCCAGGCACCTC | 11252 |
| rs186664590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993071 | CTCGGGAGCTGGGAG[C/T]TGGGAAGCAGGAGAA | 11252 |
| rs186672748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984969 | TGGATATATGTGGAT[C/T]TGCTTGTTCTGTTTG | 11252 |
| rs186676874 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013030 | GTTCTGACCTCAGGT[A/C/G]ATCTGCCCGCCTCGG | 11252 |
| rs186721316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946210 | AAAGAAGTGTTTAAA[C/T]TGCATGTGAGCATAA | 11252 |
| rs186736007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980137 | GCAAAACAAGTATAG[A/C]GTATTGGGTGAAAAT | 11252 |
| rs186738320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883781 | AAGGCCGAGGTGGGC[A/G]GATCACAAGGTCAAG | 11252 |
| rs186768041 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973073 | AGGGCAGTCATATAT[C/G]TGCCCACATACTGCA | 11252 |
| rs186776777 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012005 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGGATGCC | 11252 |
| rs186799808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916884 | CACCACAGCAAGCCA[A/C]CCGAAGGTACTCGGA | 11252 |
| rs186807601 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952541 | TTTGTTTTGTATTTT[C/T]AGTAGAGACGGGTTT | 11252 |
| rs186809728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935063 | TAGGACTACAGGTGC[A/C]CGCCACCGCGCCCGG | 11252 |
| rs186810341 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907873 | AAAGTATCACTCCAC[A/G]TGGATGATGAATATG | 11252 |
| rs186818341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971318 | TCTCCAGCTCCCGAC[C/T]GCAAGTGATCTGCCC | 11252 |
| rs186822308 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016635 | CCCTGGCGACAGTGC[A/G]AGACTCCATCTCAAA | 11252 |
| rs186826246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987984 | CGTCTCTACTAAAGA[C/T]ACAAAAATTAGCCAG | 11252 |
| rs186867370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937527 | CCTGCCTAGATGTCC[C/T]GGCTCGATCACCAAG | 11252 |
| rs186869119 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872523 | CCCCCTGGTTTAGCA[C/T]TTCCCTGATGCTTTG | 11252 |
| rs186878100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894785 | TCGCTGATAACTTGA[A/G]CACCCAGAGGAAATA | 11252 |
| rs186886478 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967802 | CTGAGGCAGGAGAAT[C/G]GCATGAACCCGGGAG | 11252 |
| rs186900723 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007201 | CCCTAGCAGCCCCTC[A/T]CACACACACCTCTTG | 11252 |
| rs186960648 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892356 | ACCCAGAGGGGGACA[C/T]GTGACTCTGGGGCTT | 11252 |
| rs186962536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934277 | TGCTCAACTGTGTGC[C/T]CAAATACCAGTCAAT | 11252 |
| rs186985048 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991288 | AGCTGGTCAAGGACA[A/G]GCAGTGGCTCAGAGC | 11252 |
| rs187057621 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955301 | AATGAATGAATGAAC[A/G]AACAAACGAACGAAC | 11252 |
| rs187109448 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887752 | GACTCCAGGACCTTC[C/T]AGGCAGAATCACTTA | 11252 |
| rs187222181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915076 | GGTCTCACTGTTGCC[C/T]AGACTGGTCTCAAAC | 11252 |
| rs187231819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940875 | AAGTACTTGAGATTC[C/T]TGCTATTTTTCTAAC | 11252 |
| rs187250769 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943716 | ATTTTGATGAATTTC[A/C]AGTGTCATAAGGAGC | 11252 |
| rs187255602 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927925 | AACGTCATGTCATGG[A/T]CCCATACTCCACTGA | 11252 |
| rs187258634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962081 | TGAGTTCTGGGGAAG[C/T]AAGTTTGAGACCAGC | 11252 |
| rs187261399 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012514 | TAAACAGAGTCTCAC[C/T]CTGTCACCCAGGCTA | 11252 |
| rs187269393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977981 | ATACAGGGGTACTCA[C/T]ACATTGCTAGTACAA | 11252 |
| rs187273763 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999592 | AGAATCGCTTGAACC[C/T]GGGACGCGGAGGTTG | 11252 |
| rs187285000 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017478 | CTGGGATTACACGCA[C/T]GAGCCACTGTACGCA | 11252 |
| rs187312687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920874 | GTGGTGTGATCACAG[C/T]TCACTGCAGCCTCAA | 11252 |
| rs187313812 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890515 | CTGAGGTCAAGAGTT[C/G/T]GAGACCAGCCTGGCC | 11252 |
| rs187319852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899849 | AAACAGAATGATGTG[A/G]GGCATGATGCCATTT | 11252 |
| rs187327633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938063 | ATACTAGATTCTAGA[G/T]GACAGCCCTAAAAAC | 11252 |
| rs187332451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973492 | GAGAAAAAGACTCCA[C/G]ATGCTTTCCCCATTC | 11252 |
| rs187334017 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955879 | CATGTGTCAGTTCAT[A/C]GCAGAGAAGATAGAG | 11252 |
| rs187346643 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992143 | TCCAAAATATATTTT[A/T]AAAATTTCAAAACTA | 11252 |
| rs187376334 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934689 | ACCCTTTGCCCACCA[A/C]TGTCCCGTTATAGTT | 11252 |
| rs187384062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966745 | TCAGTTAAGATGTCA[C/T]GCAGCCTCATGGTCC | 11252 |
| rs187385965 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997262 | AAAATTTGCTGAATA[C/G]ATAAATGGGGATTTG | 11252 |
| rs187396035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948432 | AGTGAACTACCTAAA[C/T]ACCTTCTCAACCAGT | 11252 |
| rs187398348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983054 | GGGCACAGTGGCTTA[A/C]AACTGTAATTCCAGC | 11252 |
| rs187401090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939304 | ATGGAGGCTGAACAC[G/T]TCCCCAACCTAAATA | 11252 |
| rs187412126 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004732 | ATTTCATTCAATAGG[A/C/G]AACTTCAGAATACAC | 11252 |
| rs187442363 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893290 | TTCTGGTGATGGGCG[C/T]TAATGCTCCCCATAA | 11252 |
| rs187454651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871762 | CAGCTCCATAGGGCT[A/G]TGCCTTCCTCACCAC | 11252 |
| rs187475889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956160 | CATAGCACCCTTCAC[A/G]TTAACAAAAAGATAA | 11252 |
| rs187528082 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878838 | CACCAGGCAGGAAGA[C/T]GACCTTCCCTGGAGA | 11252 |
| rs187557012 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921834 | ACCTCCGTCTCCCGG[C/G]TTCAGGCGATTCTCC | 11252 |
| rs187601278 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941878 | GACTCCTGGGTTCAA[A/G]CGATTCTCCTGCCTC | 11252 |
| rs187605374 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977326 | TATACAAAGAGTTCC[C/T]AAAAATTCAAAACAA | 11252 |
| rs187651335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951819 | GGTCCCATGTGATTC[C/T]AGCCCCTGCTTCCAG | 11252 |
| rs187659684 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015680 | TGCTCTCTCTAATAA[A/T]ATATATTTGGATGGC | 11252 |
| rs187662597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903322 | ATGTCCCCATGGTGA[C/T]AGCTTCAGGCAACTT | 11252 |
| rs187747526 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973938 | AAGTACCAAGAACAG[A/C]AGCGTAGCCTTAACT | 11252 |
| rs187799583 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901377 | TCCTTAATTCCAAGT[C/T]TGCAGTTGGCAACGA | 11252 |
| rs187867462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960038 | AGAGCTCTCTTTTCA[A/G]AAAGTGGCCAAAGAG | 11252 |
| rs187893381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998319 | TCCCAGTCTGAACCT[C/G]GTTTGGATTCTGGGC | 11252 |
| rs187921354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885040 | GGGTGCAGGAAGAAG[A/G]CATTCAAAAAAAGTC | 11252 |
| rs187921557 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927862 | AAAGTGCTACAATTA[C/T]AGGCGTGAGCCACCG | 11252 |
| rs187928915 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904211 | GCTCCCCATGCTCTG[C/T]TCCCTTGGTGCGTGT | 11252 |
| rs187929350 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884681 | AAAAACAGGAGCTCT[A/G]GATTCTGACAGACTT | 11252 |
| rs187939796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942358 | AGCACAAAAGTTCTT[A/T]ATTTTTATGAAGTTC | 11252 |
| rs187950632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961688 | TGAGGCACGAGAATC[A/G]CTTGACCCCAGGGAG | 11252 |
| rs187961267 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927489 | TCTGGCCTCAAGTGA[G/T]CCACCCATCTTGGCC | 11252 |
| rs187971578 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015380 | TGCGAGGGTGGCGCA[C/G]ATTACTCTCCCAAAG | 11252 |
| rs188018484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010708 | ACAAAGCGAGACTCC[A/G]TCTCAACAACAACAA | 11252 |
| rs188085998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967058 | GCTTCAAGTCTGGTA[C/G]GGTAGACGGACGAGT | 11252 |
| rs188092078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877192 | TTCAGCTGTGAAACA[C/T]GGTCCAGGAGCCTAG | 11252 |
| rs188094519 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005174 | TTTCACACAGGTGAG[C/G]AGTGCTCACACCTTT | 11252 |
| rs188147767 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912380 | GGGGCGAGGGGTGCA[G/T]GTGCATAAAAGGCAG | 11252 |
| rs188156514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932620 | TATCAATTTTACTCA[C/T]GAAGACCATATACTG | 11252 |
| rs188157435 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949878 | AATTGATTTTACAAA[C/T]TATTTTACATCTATC | 11252 |
| rs188161270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933232 | GGTTCCATATACCTC[C/T]CCAACTTTCCTTAAA | 11252 |
| rs188174280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967497 | CAATGAAAAGCCTTA[A/G]ACTAAAGATCTTTAA | 11252 |
| rs188178170 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983623 | GATTGACATATGAGA[A/C]TATATCAATTTTTTG | 11252 |
| rs188196989 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919055 | TGTGCACACGTATGG[C/G]ACAAGCTGCTCTTTA | 11252 |
| rs188204914 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897503 | TTCTTCCAAACATAT[A/T]AATTGCTTCATTCAC | 11252 |
| rs188221902 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891491 | CTGCAAACTCTGTCT[C/T]CCAGGTTCAAGAGAT | 11252 |
| rs188233451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986672 | CTACTTCAGGGCAGA[C/G]AGCAACATCAGTGAC | 11252 |
| rs188311940 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915433 | CTTCTGTCTGGGACC[A/G]GGATCTCATCATAGC | 11252 |
| rs188312656 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009963 | CAGCCTCTGCCTCCC[A/G]GGTTCTAGTGATTCT | 11252 |
| rs188317846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952323 | TTTATTTATTTATTT[A/T]TTATTTTATTTTATT | 11252 |
| rs188325394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885531 | GATGGAGCGCTTCCC[A/G]AGACACTGCAGGCCT | 11252 |
| rs188416335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974656 | CGGGTGGCTGAGGCA[C/T]CGTAACTGCTTAAAC | 11252 |
| rs188451675 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912239 | ATTTCACAACTTCCC[A/G]TTTCTAATCACTGCC | 11252 |
| rs188460994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948814 | GAAGAATATGGAGCC[A/C]GTTTCGTGTGACAAA | 11252 |
| rs188470500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911673 | AACAGTAAAGTGCCT[C/T]GTAGGATAAGCTGAG | 11252 |
| rs188504663 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936100 | GGGTGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 11252 |
| rs188512840 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972369 | GGACATAAACATTGC[A/G/T]GAAGGCCGCAGGGTC | 11252 |
| rs188514853 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954025 | TAGCACTTTGGGAGG[C/T]TGAGGCAGGCAGATC | 11252 |
| rs188532887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990175 | TTTTTAAACACAGCT[A/G]ATTTCTGCAGTCAGT | 11252 |
| rs188536570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009430 | ACAGAATATCACAGG[C/T]GAGAGGGAGCTTAGA | 11252 |
| rs188539261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011423 | GAGGTTCACATGAAG[A/G]TGGCCAGAGAGCATC | 11252 |
| rs188588542 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935002 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCACG | 11252 |
| rs188604075 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893157 | AAGGCCTTCCACGTG[A/G]TAGGAACTTACCCGA | 11252 |
| rs188605323 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905429 | CCTGTGACCTCAGAC[A/G]AAATAAACTCTGGGT | 11252 |
| rs188644137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939898 | AACAGGAGATGGCAG[C/T]GTGCAAGATAAAGTC | 11252 |
| rs188668291 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931906 | TTTCAAAGCTAAAAT[A/G]AAAACGTTTAATGTT | 11252 |
| rs188674990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974894 | TGGGAATTAGTCCTC[C/T]TTTCCTTTCCTCTCC | 11252 |
| rs188680247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42995208 | CTGCAGAGAAACTGC[A/C]CCCTGGCATTCAGTC | 11252 |
| rs188683628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014227 | TGAGTCTGGGGAAAC[G/T]CTGAGGAGGGTCACA | 11252 |
| rs188688380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957540 | ATTTCAGAGGATTCA[A/T]ACTGAATTTTTAGCA | 11252 |
| rs188732903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923855 | CAGCCTAGGCAAGAT[A/G]GTGAGATCCCATCTC | 11252 |
| rs188740634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013384 | GTAGTGGCCTCATAT[A/C]TCAACCAGCATAACC | 11252 |
| rs188758332 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889920 | CGTCAAAGGGACTTG[A/G]AAAAAAAATAAAGTG | 11252 |
| rs188796959 | snp | A/C/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896122 | CACCTCCACAGCAAG[A/C/G]AACAGGACACTTCCA | 11252 |
| rs188826812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935976 | CCCAGCACTTTGGGA[A/G]GCCGAGGTGGGTGAA | 11252 |
| rs188877032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874047 | CTTCGGCCTTGGCCT[C/T]GCAAAGTGCTGGGAT | 11252 |
| rs188887435 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979965 | CATACAATACACATA[C/T]AGTATAAATACACAT | 11252 |
| rs188901599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003334 | AATATCGGCTGGGCG[C/T]GGTGGCTCACGCCTG | 11252 |
| rs188940657 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901448 | GATTTCCCAGCCCTA[A/G]CAAGACCTCCTTCCC | 11252 |
| rs188953451 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879774 | CAAATAAAGCCACTG[C/T]AAATAAAACCAGGGC | 11252 |
| rs188953805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923282 | GTCTATTCTCAACAC[A/G]GTGACCCTCTCAAAA | 11252 |
| rs188993247 | snp | C/T | 0.0543475 | 0.155628 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996261 | GTATGACACTGGACG[C/T]GGTGGCTCACGCCTG | 11252 |
| rs189007350 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993719 | AGGAATGCCCCTGAA[A/G]GCCGACCAGAGCCGA | 11252 |
| rs189015276 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973426 | GAATCTGTACCACAC[A/T]GTTTTTTGTCAACAA | 11252 |
| rs189046852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881389 | TTGCTCAGCTTCCCA[C/T]AGGTGGTCAGAGGTG | 11252 |
| rs189054729 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924470 | CTCTGAACAGTGTGA[A/C]CCTCTCAAAATGCAA | 11252 |
| rs189062792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959033 | TACATTTTGTTACCC[A/G]ACAAAAATATAAACA | 11252 |
| rs189174566 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017104 | CAGTGAGCTGATATC[A/G]CGCCACTGCACTCCA | 11252 |
| rs189212638 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874820 | GGCTTGGCAGCACCT[C/T]ACTATTTCTGAGTCT | 11252 |
| rs189215285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944463 | CAGAAATGTACTCTA[A/G]CATTGCTAATAGGCT | 11252 |
| rs189254426 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977475 | TAAAAGTGCTCCATA[C/G]AAACAGAATGGTGAA | 11252 |
| rs189269152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975272 | CATTAGAGAAAGTCC[C/T]CATTCTTGTGGTTTA | 11252 |
| rs189324343 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902339 | TGCTGCCCCAGGACG[C/T]TTCCCCCACAGATTA | 11252 |
| rs189352802 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006192 | ATGAAAAAGGACCCT[C/G]CTCAGAACCCAACCA | 11252 |
| rs189352926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940428 | CTGTCAACAGGAATA[C/T]GGATTACACCAGGTA | 11252 |
| rs189421217 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967742 | AAATACAAAAAATTA[A/G]CCGGGCGTGGGGGTG | 11252 |
| rs189439275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984204 | CTCAAACTCCCAAAC[C/T]CAAGTAATCTGCCTG | 11252 |
| rs189443992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006684 | GCCCGGCATGATGGC[A/G]CATGCCTATAATCCC | 11252 |
| rs189457286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886724 | GAAGGGTGGTGGGGA[A/G]GGACTGGCCTCCTCT | 11252 |
| rs189485195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928655 | AAAATAGTGGTGGAG[A/G]CACTTGTAGGTAATC | 11252 |
| rs189499414 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962780 | AAGGTGTGGGCGGGG[C/G]GGGGGGGCGGCGCAG | 11252 |
| rs189525418 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951451 | TGCCTCCTCACTCAG[C/T]CTCTCCCTGAGCTCC | 11252 |
| rs189531684 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979290 | GCACTTTGGGAGGCA[C/G]AGGCAGGTGGATCAC | 11252 |
| rs189533494 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934546 | TTGCCCCTCATGGGC[C/T]GGCCCTGATAGCCAC | 11252 |
| rs189535659 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969015 | ATGTGAGCCAATTCC[C/T]CTAATAAACTGCTTC | 11252 |
| rs189546827 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986176 | AGACCAGGAACTATG[C/G]TAGGAGATTTAAAAG | 11252 |
| rs189561238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007994 | AGCTTAATGGAGTGC[C/T]CCAGCTGGCTGCAAC | 11252 |
| rs189566209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929437 | AGATGCTGTCAATAG[C/T]TTCTGAGAACTGAAA | 11252 |
| rs189574888 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906455 | ATTCTGAAGAGTCAC[A/G]AGATTCAGGGTCAGC | 11252 |
| rs189578920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944820 | GTGAGGACTGTAGCT[A/G]GGCGCGGTGGCTCAC | 11252 |
| rs189584565 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988866 | AACTTAAATCCATGA[A/T]CTGAAAGGTGGTCAA | 11252 |
| rs189594801 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979472 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 11252 |
| rs189598990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963146 | TTCATTCAACAAACA[A/T]TAATGCCAGGCACAG | 11252 |
| rs189608918 | snp | A/G/T | 0.00478364 | 0.0487146 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914276 | CTGGCTCTGTTGCCC[A/G/T]GGCTGGAGTGCAGTA | 11252 |
| rs189615389 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892536 | ACAGCTTGATCCTGG[A/G]AGAGGGGCTGCAGCA | 11252 |
| rs189630430 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887266 | CTCTCGTGTAGATGA[C/T]GTGTTCCCCTTGCTA | 11252 |
| rs189643615 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007304 | TCACTGCAATCTCTG[C/T]CCCCAGGTTCAAGCG | 11252 |
| rs189705796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934331 | TTCTACGGGAAACGC[A/G]AGACCTTCAAGGCAC | 11252 |
| rs189739288 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968122 | GTAGCGCGGGAAGCT[C/G]CAACCCTGGCTCCCT | 11252 |
| rs189790957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901679 | CCTGCCACGGCGATC[A/G]CCTGACAAGGCCTAA | 11252 |
| rs189796215 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989763 | CTGAGATCGCGCCAC[C/T]GCATTCCAGCCTGGG | 11252 |
| rs189809957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000060 | ACCAATCTCAGAGCT[A/G]GGATTCAAGCCCAGG | 11252 |
| rs189869610 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953332 | AAAATGGGCATGATG[A/C]AATGCAATCAAAACA | 11252 |
| rs189971450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951227 | GAATCCACGAGCCTT[A/G]TCTTCTAGTCACGAT | 11252 |
| rs189987961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984981 | GATTTGCTTGTTCTG[C/T]TTGGCAACCAAAGGT | 11252 |
| rs190013565 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913301 | CCTGACCAAGACGGA[A/G]AAACCCCGTCTCTAC | 11252 |
| rs190039349 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880419 | AAATTCATCCTGATT[G/T]GGTGGCTTCCAAAGG | 11252 |
| rs190051554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011127 | CGCATCTGGAGTCTG[C/T]CTGGGGCAGGGACGA | 11252 |
| rs190056596 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909357 | AACACAAAAAACTTT[G/T]CCACCTCAAGACCAC | 11252 |
| rs190073118 | snp | A/G/T | 0.000231971 | 0.0107676 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888637 | AAAAACAAGTGTACA[A/G/T]TTTACCTTAAGAACA | 11252 |
| rs190142464 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972007 | ACCCCGTCTGGGAGG[A/T]GTACCCAGCAGCTCA | 11252 |
| rs190151620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973531 | AATGTTTCATTCAAT[C/G]AGAAACTCTACATAT | 11252 |
| rs190158163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955893 | TAGCAGAGAAGATAG[A/G]GAAGTCATTTCATTA | 11252 |
| rs190169687 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992858 | AGACTAAAAATAACA[C/T]ATACTGTAAAAAGAA | 11252 |
| rs190173799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012836 | ATTTTGTATTTTTAG[C/T]AGACATGGGGTTTCT | 11252 |
| rs190221057 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892396 | AGAGAACAGCCCCGG[A/T]AGTTGGACCTCTCTG | 11252 |
| rs190225203 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913836 | GTAATATTCTCTCCA[C/T]TACACCAAGATGTTT | 11252 |
| rs190276858 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892141 | TCCCCGAGGCTCAGG[A/C]AGGAAGCCCTAATCC | 11252 |
| rs190284858 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933486 | GAGCAACAGAACACA[C/T]CCATGTTCATGTTTG | 11252 |
| rs190289920 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869505 | CCTGCTGTTTGGGCT[A/G]GGGCAATAGAGAGGC | 11252 |
| rs190304763 | snp | C/T | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959733 | GAAAGAAAACAATTC[C/T]GTGAAAATTCTACTT | 11252 |
| rs190311189 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977189 | AAGAAATAGAAATAG[A/G]AATTTGCAAAAAATC | 11252 |
| rs190313322 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998059 | CCCAAACATATCCAA[C/G]GGCAGTTACCAGCCT | 11252 |
| rs190330188 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016192 | AAAAGTAAAATAAAA[A/G]AAAATAATAATAAAA | 11252 |
| rs190343369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950286 | ATTTTATATCAGAGA[C/T]GAGCATCCATGGATT | 11252 |
| rs190387831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941434 | CTGCTGGGTCATAAT[A/G]AGAAACTTCCAAAGT | 11252 |
| rs190444956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964495 | ATAGAATACCACAGA[C/T]TGCAGTTCTGCGCTC | 11252 |
| rs190446933 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920592 | AGGTGGAAGCTGTAA[C/T]AACGCAGAAACAAGG | 11252 |
| rs190459074 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955317 | AACAAACGAACGAAC[A/G/T]AACGAAAAAACAAAT | 11252 |
| rs190506352 | snp | A/G | 0.441432 | 0.160792 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971866 | GGGCAGCCCCCGCCC[A/G]GCCAGCAGCCCCGTT | 11252 |
| rs190515567 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876518 | TCCTGAGCCATCAAC[A/C]GGCTTTCCAGGGGCA | 11252 |
| rs190528229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899442 | ACAGCAGGCAGAGCA[C/T]ACAGAGACACCTCTG | 11252 |
| rs190535501 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001751 | TTTTGCCCACAGTAA[G/T]GCAAGAGAACTAAAA | 11252 |
| rs190570706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895802 | ACAGAGCCAACGGGA[A/G]AAGGGCAGTATGCCA | 11252 |
| rs190605260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927734 | CTGGGATTAGAAGCA[A/T]GCACCACCACGTCTG | 11252 |
| rs190615439 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960538 | CCTCGCTTCTTCAAT[G/T]TTTACAAAGAATTTA | 11252 |
| rs190666501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883669 | GACTGTCCCAGGCAC[A/G]ACCAGCCCAGAAATG | 11252 |
| rs190747417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952854 | GTTTTTTAGTAGAGA[C/T]GGGGTTTCTCCATAT | 11252 |
| rs190792108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872714 | TGTGGACTGGGGGTA[C/T]TGTGAAGATTAAGTG | 11252 |
| rs190803624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986544 | TTCACGGAGGCCTTT[C/T]GGGGCCCTGCACGCT | 11252 |
| rs190809126 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008568 | TTCAGTGTTCTTTTA[A/C/G]ATATATGAGCTCTTT | 11252 |
| rs190811689 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917561 | TCAAGGCTGCAGTGA[A/G]CTATTATTGTGCCAC | 11252 |
| rs190838787 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903479 | AACCATCTAGTCCGT[G/T]CCTTGCTTTCAGGTG | 11252 |
| rs190868490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942225 | GATTACAGATGTGAG[C/T]CAATGCACCCACCCA | 11252 |
| rs190884878 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977352 | AACAATCCAGTAGAC[A/G]GAAAAACGGAGAAAG | 11252 |
| rs190925186 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870196 | AACTACTGCAAAGAC[A/G]CGGGCACTTTTACAG | 11252 |
| rs190931274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998688 | CAGAAGGGCAGGGTC[C/G]CTGGTGAGAGCCCCA | 11252 |
| rs190944686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947975 | CACTTGAACAACCTC[C/T]TCCAACACAGCGGCC | 11252 |
| rs190950773 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931265 | AAACCAGCTGGGTAA[C/G]CAGGGGCACGTTACT | 11252 |
| rs190964749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011838 | CCAACATGGTAAAAC[C/T]CCATCTCTATTAAAA | 11252 |
| rs190964915 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966335 | GTGCCCCTGCACTCC[G/T]GCCTGGCGACAGAGT | 11252 |
| rs190968838 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982972 | GATCACTTGAGGTCA[C/T]GAGTTCAAGACCAGC | 11252 |
| rs190970432 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004515 | GCCAATCAGACAGCT[A/G]CAGAACCCACTAATA | 11252 |
| rs190990417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926525 | GGAAGGGGAATCTTA[A/G]GAACTCCACGAGGAC | 11252 |
| rs191010811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940988 | ACATCATGACAATCA[C/T]TTTAGAACATTTTCA | 11252 |
| rs191018983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959476 | TTTTGAAAGGAAACA[A/C]GCACGTATGTTCTAA | 11252 |
| rs191032218 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889398 | CACACACACACACAC[A/T]CTCTTAACAGATCCT | 11252 |
| rs191032422 | snp | C/G/T | 0.00279242 | 0.0372774 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910367 | CAAGGGCCTGCACTT[C/G/T]TAAAGGCTGGAGAGC | 11252 |
| rs191100660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884784 | GGAGCAAGGCCCAGA[C/T]AGGTAGATGCCGGCA | 11252 |
| rs191168344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947177 | TAGAATGGGTCAGGA[A/G]GCTGCCCTTTGTTCA | 11252 |
| rs191178511 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980268 | CCTATAATCCCAGCA[A/C]TTTGAGAGGCCAAGG | 11252 |
| rs191185681 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017024 | CGTGGTGGCGGTCGC[C/T]TGTGGTCCCAGCTAC | 11252 |
| rs191256573 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916983 | TTGGTGACGCTGCCA[C/T]CTGCCACTGTGACCT | 11252 |
| rs191315718 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902946 | TCCTGCGAGTCACAC[A/G]AGCTCTCTCCATGGT | 11252 |
| rs191326266 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003853 | TCCTGTCCCACGTGG[G/T]ATGCATCATGGGGTG | 11252 |
| rs191390881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931007 | GGCAGCATGCCAACC[C/T]GAGTCCAACAAGAGT | 11252 |
| rs191415314 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964949 | TGGTTCATTTATTTG[C/G]TAGTTCCCTCTGCCT | 11252 |
| rs191443530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888405 | ACCAAGAGCTGTCTC[C/T]TACCCCTGGCTTGCC | 11252 |
| rs191476837 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930114 | CATCGCGAACCATGA[A/G]GTGACTTGGGAACAG | 11252 |
| rs191529712 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883875 | TGGGTGTGGTGGCGC[A/C/G]TGCCTGTAATCCCAG | 11252 |
| rs191577046 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971605 | GGGAAGTGAGGAGTG[A/T]CTCTGCCCAACCGCC | 11252 |
| rs191595386 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988234 | GGCACCAAAGACAAG[A/G]AGAAGATAGTCTCTG | 11252 |
| rs191599875 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010575 | ATTAGCCAAGTGTGG[C/T]GGCGGGCGCCTGTAG | 11252 |
| rs191655519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973112 | ATCTGGGACATGACC[A/G]TCAGCTCAAACAAGA | 11252 |
| rs191682268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978732 | ATATTCAAAAGTATG[G/T]TTGCATCCTGGCCCT | 11252 |
| rs191692063 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933051 | CAGCATTTATATTTA[C/G/T]AGTAGAATTTGAAAA | 11252 |
| rs191697644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999599 | CTTGAACCCGGGACG[C/T]GGAGGTTGCCGTGAG | 11252 |
| rs191701262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912267 | GCCTTCAGTACAGGG[C/T]GGTCTATAATATTTC | 11252 |
| rs191705815 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017490 | GCACGAGCCACTGTA[C/T]GCAGCCTCTCCCAAG | 11252 |
| rs191716023 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907901 | ATGAAGGTGTTCTCA[C/G]GTGATGAGCTGTCCT | 11252 |
| rs191725678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946164 | TTCAAAAGCAAAATA[A/G]TAAGAATCCTTCCAA | 11252 |
| rs191764738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890666 | GTTGCAGTGAGCTGA[A/G]ATTGCACCACTGCAC | 11252 |
| rs191774179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938224 | TCCTGGGCTCGCGAA[A/G]CAGCAGAAGGTATGA | 11252 |
| rs191776214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962145 | AAAATACAAAAATTG[A/T]CTACCTGTTCCCTCC | 11252 |
| rs191833219 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915740 | ACAAGGCATTTCAGA[A/C]CCAACAGAAATTACT | 11252 |
| rs191842639 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935009 | CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT | 11252 |
| rs191885924 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015683 | TCTCTCTAATAAAAT[A/G]TATTTGGATGGCAAG | 11252 |
| rs191905311 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901541 | TACAAGTCCCTCTCC[A/G]TATATTTCTGCCCTT | 11252 |
| rs191922535 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880090 | GAGCTCTCCTTCCCC[C/T]CATCTCCACCAGTTA | 11252 |
| rs191924518 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923365 | CAGGTCCTCCTGGCC[C/T]GCAGGCCCGCATCTG | 11252 |
| rs191936363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915135 | GGCCTCCCAAATTGC[C/T]GAGATTACATGGATG | 11252 |
| rs191941118 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871127 | GTGGGCGGGGAGGGG[C/T]GGCTATTTCTGTTGT | 11252 |
| rs191948364 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976008 | TTCCAGGCCAGTCTG[G/T]AAGGTCCAATCTGAG | 11252 |
| rs191965355 | snp | C/T | 0.000880475 | 0.0209634 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951859 | CGCTCCTTCCAATCC[C/T]CACACCCTGGACTCT | 11252 |
| rs192011167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972827 | TCAGCCTCCTGTGTA[C/T]CTGGATTACAGATGC | 11252 |
| rs192038503 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012064 | GCAGGGGAATCACTT[A/G]AACCTGGGAGGCAGA | 11252 |
| rs192059305 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898719 | CAGGACTCGCCCTGC[C/T]GCCTGCCCTCCTCCA | 11252 |
| rs192064374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937406 | GTGAGCCCAGGCAGG[C/T]GGCAGTAGAAATAAC | 11252 |
| rs192170586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895209 | TCCTGTGAGGAAGTC[A/G]GAAGTGAGCATTTTC | 11252 |
| rs192192098 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969775 | AAGAACCCATCTCTA[A/C/T]GAAAAATTTTTAAGC | 11252 |
| rs192241881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893171 | GATAGGAACTTACCC[A/G]AGTTCTGAGTTAACT | 11252 |
| rs192259317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939422 | AGAATTCAAACAGTA[C/G]TGTAAGAAGATGTAC | 11252 |
| rs192261170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983128 | TCGAGACCAGCCTGG[C/T]CAACATGGTAAAACC | 11252 |
| rs192263595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974715 | GATTGTGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 11252 |
| rs192265438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005107 | AAACAAGGAGAAACT[G/T]CCTATAATTCTAAAG | 11252 |
| rs192269434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957792 | TTTCAAAGAAGAATT[A/G]AGTGCTTGTCTGTTT | 11252 |
| rs192270480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934700 | ACCACTGTCCCGTTA[C/T]AGTTCCTCTATGGTG | 11252 |
| rs192291940 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997537 | CACTCCAGCCTGGGC[A/G]ACAGCGAGACTCCGT | 11252 |
| rs192353274 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990678 | TGTGGCAAGAGATGA[C/G]ACTCAACGGGTAAGC | 11252 |
| rs192398411 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942684 | TTTCCCCCATTGAAC[C/T]GGCTTAGCATCCTTG | 11252 |
| rs192403985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010848 | GGGAATAAGCACAAT[C/T]CAATAGGTAACTTAA | 11252 |
| rs192415931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977652 | CGGCAAATTGTAATC[C/T]CTGTGTGGCAGGGGA | 11252 |
| rs192417893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961765 | GTGACAGAGCGAGAT[C/T]CTGTCTCAAAAAAAA | 11252 |
| rs192422722 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875692 | AGATGCCCCGCCACA[C/T]GCCTGGCTCATTTTT | 11252 |
| rs192441766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919715 | GAAGTGGAGGTTGTA[A/G]TGAGCCGAGATTGCA | 11252 |
| rs192443725 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955008 | TGCATATATTGCTCC[C/T]GCTGCTTCTCTTGGG | 11252 |
| rs192481413 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927876 | ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCTCAGT | 11252 |
| rs192486814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885160 | AATGTTAAAAAGCAG[A/G]TGTGGCCTATCTCAA | 11252 |
| rs192491583 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904474 | GCTGGAAGAGCTGCC[A/G]TGGCGAGATCACCTG | 11252 |
| rs192513064 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000114 | CTAACAACAGCTCAC[C/T]GCAGGCACTTGTAGC | 11252 |
| rs192518499 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872568 | GCAATGCTGGTCAAC[A/C]TGCCTGCGGAGCTAA | 11252 |
| rs192518950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967659 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 11252 |
| rs192530008 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983826 | TTGTTCTTCAGTTAA[C/T]TGACTGGTGGTCAGT | 11252 |
| rs192542923 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006381 | CTAGTGATGGAGCTC[C/G]AACCCACACCCAAGG | 11252 |
| rs192589680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949891 | AATTATTTTACATCT[A/C]TCTCTCCCAATATTC | 11252 |
| rs192639929 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949592 | TACAATATACAATAA[C/T]ATTATCTGAGAAGCC | 11252 |
| rs192640790 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878867 | GATGCCCCTGGGCCA[C/T]GGCCCACAGAGCTCA | 11252 |
| rs192675005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877407 | GGGTCTCCTCTGAGA[A/G]TGACAGTGTGGGAGG | 11252 |
| rs192690262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920996 | AGACGGGGTTTCGTC[A/G]TATTGCCCAAGCTGG | 11252 |
| rs192739273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905648 | GGAATGGCTGAGCAC[A/G]CAGGCCGAAGACAAT | 11252 |
| rs192744239 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943846 | TGTGTCCAAAACTTA[C/T]GTTAAACTTTTGCAC | 11252 |
| rs192748174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970672 | CAGGGACAATGTGGT[C/T]TTCTTTTTAAAATTT | 11252 |
| rs192751602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009823 | CATTTTTAAGGCTTC[C/T]TGCGAGGTCTTTGAT | 11252 |
| rs192804523 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889957 | AGTTTATTGAGAAAG[A/T]AAAGGAATAAAGAAA | 11252 |
| rs192820992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931928 | TTTAATGTTTTCCCA[C/T]GGAAACTCAACGTTA | 11252 |
| rs192824124 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966746 | CAGTTAAGATGTCAC[A/G]CAGCCTCATGGTCCT | 11252 |
| rs192880139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967126 | CAGAAACTAGGCAGG[A/G]AATGTGGAAGGTGGG | 11252 |
| rs192888273 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005185 | TGAGCAGTGCTCACA[C/G]CTTTATCATTTGCTT | 11252 |
| rs192905627 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900597 | TCCTGCCTCAGCCTC[C/T]GAGTAGCTGGGACCA | 11252 |
| rs192944480 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952363 | TTTATTTTTAAGTTT[A/T]TCTTTTTTTTGAGAC | 11252 |
| rs192948897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885687 | CAACTCCTCTTCTTG[A/G]AGCCTTCCCCAGCCT | 11252 |
| rs192953701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927946 | ACTCCACTGAGCCGA[A/G]CCCTCATGTCCAGAT | 11252 |
| rs192958955 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987667 | GTCCCAAGTAGCTGG[G/T]ACTACAGGTGCGCAC | 11252 |
| rs192990318 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993765 | TTCATCTCCACATCC[A/C/G]ACCTGGCAGTTCCTC | 11252 |
| rs193020132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911696 | AAGCTGAGCAATTAG[C/T]GTCTGTCTCTCCCAC | 11252 |
| rs193033063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948452 | TCTCAACCAGTACTA[A/T]AAATATGTGCCTTTG | 11252 |
| rs193064659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917621 | CCCTATCTCAAAAAA[A/C]CCAACCAAACAAAAA | 11252 |
| rs193068502 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952806 | TAGCTGGGATTACAG[A/G]TGTGTGCCACCAGGC | 11252 |
| rs193069876 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952900 | TGAACTCCTGACCTC[A/G]AGTGATCCACTGGCC | 11252 |
| rs193071734 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017305 | TCAAGCCATCCTCCT[A/G]CCTCAGCCTCCCAAG | 11252 |
| rs193074087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989121 | TAGGCTCACGAAATC[C/G]TCCTGCCTTGACCTC | 11252 |
| rs193092369 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872767 | GAGGGTGGGACATGC[A/G]TAAGCACTGGCTCAG | 11252 |
| rs193098579 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013038 | CTCAGGTGATCTGCC[C/T]GCCTCGGCCTTCCCA | 11252 |
| rs193112774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901390 | GTCTGCAGTTGGCAA[C/T]GAGACGGGCAAAATG | 11252 |
| rs193115357 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938461 | TTCCCATGACCTTAG[A/C]GGAAAGGAAGGTCAG | 11252 |
| rs193124521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974155 | TCTATGTAAGTCTCC[C/T]TCCCTCCGTATCCCT | 11252 |
| rs193149307 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987449 | CCTGAGTCCAGGAGC[A/C]ACACACACACACACA | 11252 |
| rs193202339 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013504 | CTGGCACAGCTTCAA[C/T]GTCTCCATGAGGAGG | 11252 |
| rs193230755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895904 | CGGTGAAGGCCATCA[A/C]TGGAAGTCTCTATCG | 11252 |
| rs193232156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935297 | GATTATCGAGGACCT[A/G]CCTCCTCCCTGTTTC | 11252 |
| rs193237416 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999176 | ACAACCCTAGACACT[C/G]CTGTGGGGCCAGAGC | 11252 |
| rs193254880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993706 | TTCTGAGACTGGCAG[A/G]AATGCCCCTGAAGGC | 11252 |
| rs193270716 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922000 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 11252 |
| rs193272217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956211 | GATGACCACTGGCAC[A/G]CATTTCAAATTAATT | 11252 |
| rs199523028 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983332 | AAAAAAAAAAAAAAA[-/G]AAAAGAAACTGGCTG | 11252 |
| rs199535946 | snp | C/T | 0.000916868 | 0.0213914 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879014 | GCCCCCACCATGGAA[C/T]GGCCTCTTTTGGATG | 11252 |
| rs199554903 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963846 | AATAAAATTTCTACA[A/T]TTTTTTTTTCACCAC | 11252 |
| rs199625199 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875801 | TTGGCCTCCCAAAGG[-/T]GCTGGGATTACAGGC | 11252 |
| rs199639425 | snp | A/C | | | missense | PACSIN2 | GRCh38.p7 | 22:42884487 | GCACTGCTCAAACAC[A/C]TGCTCCATGTTCTCC | 11252 |
| rs199640673 | snp | A/C/G | 6.78626e-05 | 0.00582472 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893633 | GAGAGAGAACCAGCT[A/C/G]GGAGGCAGGGGGCTT | 11252 |
| rs199686041 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989883 | ATATATATATATATA[C/T]ATACACACACACACA | 11252 |
| rs199698770 | snp | A/C | 0.00120809 | 0.0245504 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876102 | CCTGCAGGTTGGAAG[A/C]CCTCCTCCCCTGGAT | 11252 |
| rs199785617 | snp | A/C | 0.000102499 | 0.00715815 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891181 | GGTCCCGTACTGGGG[A/C]CCTGTGCAGGGGAGA | 11252 |
| rs199789311 | snp | A/G | 0.448836 | 0.15154 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42981792 | GTGGGTCAGCCCCCC[A/G]CCCGGCCAGCCGCCC | 11252 |
| rs199798313 | snp | A/C | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871935 | GCAACTTCCAGGCTG[A/C]GAGGGGAAGGGACCA | 11252 |
| rs199829511 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964418 | GCGAGACTCCGTCTG[A/G]AAAAAAAAAAAAAAA | 11252 |
| rs199855014 | in-del | -/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942858 | AGCCCTCCAACTTTG[-/TT]CTCTGACTTTTCAAA | 11252 |
| rs199901520 | snp | A/G | 1.6797e-05 | 0.00289797 | missense | PACSIN2 | GRCh38.p7 | 22:42891167 | CAGGCCTTCTCCACG[A/G]TCCCGTACTGGGGCC | 11252 |
| rs199924838 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971919 | ACCCGGCCGCCGCCC[C/T]GTCTGGAAGGTGGGG | 11252 |
| rs199938348 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952173 | TTGCCTTGTTTGCCC[C/G]TGTTCCTACCACTGA | 11252 |
| rs199952474 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965945 | TAAATAAATAAATAA[A/T]CATAAATAAATTATG | 11252 |
| rs199952577 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990045 | ATATATGTATATATA[C/T]ATATATACACACACA | 11252 |
| rs199966964 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972274 | ATTAAGGGCGGTGCA[C/T]GATGTGCTTTGTTAA | 11252 |
| rs199982121 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962197 | ACTTTTTTTTTTTTT[G/T]TCCCAGAGCCCCACT | 11252 |
| rs200030603 | snp | G/T | 0.446118 | 0.155041 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990831 | CCATGGAAACCACTC[G/T]ATTTGGCTCAAGAGC | 11252 |
| rs200047970 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989868 | GAGGGGGAAAAAAAA[-/AT]ATATATATATATATA | 11252 |
| rs200065690 | in-del | -/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952663 | CACCCGGCCTATTTA[-/TT]TTTATTTTTTTTTTT | 11252 |
| rs200157900 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917631 | AAAAAACCAACCAAA[-/C]AAAAAAAAAAGTGAA | 11252 |
| rs200159771 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969933 | AAAAGAAAAAAAAAA[-/G]AAAAGAAACTAGAAT | 11252 |
| rs200207353 | snp | A/G | 0.00046558 | 0.0152504 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879077 | CGGCAGAGACTGGTC[A/G]CCTGTCTGGTTGATG | 11252 |
| rs200235214 | in-del | -/AAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974817 | GAGGAAGAAAAGAGA[-/AAG]AAGAAGAAGAAGAGG | 11252 |
| rs200272554 | snp | C/T | 0.46137 | 0.133501 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42981096 | ACGTCTCTGCCCGGC[C/T]GCCCATCGTCTGAGA | 11252 |
| rs200278780 | snp | C/T | 8.3248e-05 | 0.00645113 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871350 | CCGCTGGCCTGTCCC[C/T]GACTCATCACTGGAT | 11252 |
| rs200291520 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963937 | TGAGATATAATTCAC[A/G]TCACACAGTTCACCC | 11252 |
| rs200348918 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982887 | AAAAAAAAAAAAAAA[-/C]AAACAACAACAAGGC | 11252 |
| rs200353380 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926685 | AGGAAAAAAAAAAAA[A/T]TCATTCTGGAGCTGA | 11252 |
| rs200361801 | snp | A/G | 0.000200406 | 0.0100081 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871509 | TCCATGAGAGGTATG[A/G]CACCGACGGTGGGCT | 11252 |
| rs200405612 | in-del | -/CTA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009863 | ATCATTTTATTTTTT[-/CTA]TTTTTTTTTTTTTTT | 11252 |
| rs200408154 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922777 | GGAGGGGCAGTGGAC[A/G]AGGCAGACTGGGTCC | 11252 |
| rs200427054 | snp | G/T | 0.00355156 | 0.0419901 | missense | PACSIN2 | GRCh38.p7 | 22:42884398 | TACCCAGCCACATTG[G/T]ACAGGTCTAGGTGCT | 11252 |
| rs200468243 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887619 | GCAATCACACCCCCC[-/A]AGCCCTCACCCCTCA | 11252 |
| rs200478218 | snp | A/G | 0.000331351 | 0.0128672 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42882220 | GGCCATGCCCGGCCC[A/G]TGATTGGCTCGGAAC | 11252 |
| rs200485201 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969922 | AAAAAAAAAGAAAAA[A/G]AAAAAAAAAAGAAAA | 11252 |
| rs200500178 | snp | A/C/T | 4.97726e-05 | 0.00498841 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912078 | ATCATATGTGACAGA[A/C/T]ATTTTTTCAAAGGCT | 11252 |
| rs200526238 | in-del | -/TAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987027 | GACGCCTTCCCTAAC[-/TAA]CACCCCTCAGACAGC | 11252 |
| rs200532155 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948221 | GCTGTGAAGGAGGGG[C/T]GAGGGGACTGACAAA | 11252 |
| rs200536202 | snp | A/G | 0.000398552 | 0.0141109 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876321 | GCTCTGGGTCTTCTC[A/G]TAGCTGCTCACACTG | 11252 |
| rs200568144 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903550 | TCCACTCGTCCTGGT[-/C]CCCCAAACTTCCCAC | 11252 |
| rs200648208 | snp | C/T | 0.000217848 | 0.0104344 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871516 | GAGGTATGACACCGA[C/T]GGTGGGCTACAGAGC | 11252 |
| rs200677892 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988898 | GAAATTTTTTTTTTT[-/G]TTTTTGGGAGTGAGT | 11252 |
| rs200693723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893404 | CGTGCCCAGAGCCCC[C/T]GGCTGGGGTGTAGCT | 11252 |
| rs200715630 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983489 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA | 11252 |
| rs200720069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983360 | CTGGGTGTGGTGGCA[C/T]ACACTTCTAATCCCA | 11252 |
| rs200775876 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894930 | ATGGGCAAGGGGAGG[A/G]AAGGGGGCTGCAGCA | 11252 |
| rs200803740 | snp | C/G | 3.31691e-05 | 0.00407228 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876848 | AGGAAGAGAGACAGA[C/G]TGAGCGCGGTGGGAG | 11252 |
| rs200823245 | snp | A/C | | | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893570 | TCGCTGCACAGGCGG[A/C]GGCCATCGTCGATCC | 11252 |
| rs200850739 | snp | A/G | 0.000191875 | 0.00979289 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890918 | AGGCAGAGCAAGGCC[A/G]GGCAGGGAAGCCTGC | 11252 |
| rs200869059 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963933 | TATTGAGATATAATT[-/CA]CACGTCACACAGTTC | 11252 |
| rs200886149 | in-del | -/TGAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955275 | ACCAAGAAGGTAAAC[-/TGAA]TGAATGAATGAATGA | 11252 |
| rs200898876 | snp | C/T | 0.0082993 | 0.0638809 | missense | PACSIN2 | GRCh38.p7 | 22:42879076 | TCGGCAGAGACTGGT[C/T]GCCTGTCTGGTTGAT | 11252 |
| rs200927202 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012154 | GTCTCAAAATAAATA[A/C]ATACATACATACATA | 11252 |
| rs200999208 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940846 | AGGAGAGGCTGTGGG[A/G]GGGATGATGGGTGAA | 11252 |
| rs201008887 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954490 | AGCCTCAACCTCCTG[C/G]GTGTAAGCGATCCTC | 11252 |
| rs201034705 | snp | C/T | 0.000581729 | 0.0170448 | missense | PACSIN2 | GRCh38.p7 | 22:42891147 | CCTCGGACATGAAGG[C/T]CATCCAGGCCTTCTC | 11252 |
| rs201041682 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979693 | ATATGCTCTGTCTTA[-/T]AGGCACCTGCCGCTT | 11252 |
| rs201082153 | snp | C/T | 6.64275e-05 | 0.00576276 | missense | PACSIN2 | GRCh38.p7 | 22:42879109 | CCGTCAGGGTGACGC[C/T]GTCAGTGGCCTTCTT | 11252 |
| rs201150880 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991990 | CCAACCAAAAAAGCA[A/C]AAGCCGTAAAAGAAC | 11252 |
| rs201210111 | in-del | -/AACCACCACG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007364 | GGGTTCACAGTCACA[-/AACCACCACG]CCCAGCTAATTTTTG | 11252 |
| rs201219931 | snp | C/T | 0.000100222 | 0.00707821 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42893512 | GAGCTGCTGCGCATA[C/T]GCCTTCTCGATGCGC | 11252 |
| rs201221909 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934924 | TCCTTTTTCTTTTTC[-/T]TTTTTTTTTGAGACA | 11252 |
| rs201241043 | in-del | -/CA | 0.0441095 | 0.141807 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949468 | ACACGCGCGCGCACG[-/CA]CACACACACACACAT | 11252 |
| rs201246480 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923643 | CGTGTCAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 11252 |
| rs201283641 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942747 | TAGTTTTGTTTTCTT[-/G]ACTCTATCTCATTTT | 11252 |
| rs201337087 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010727 | CAACAACAACAACAA[-/C]AAAAAAAGACAAGAA | 11252 |
| rs201339541 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962183 | CAGGATACCAGAAAA[C/T]TTTTTTTTTTTTTGT | 11252 |
| rs201352879 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974784 | AAGAAAAGAGAAGAA[-/G]GAGGAGGAGGAGGAG | 11252 |
| rs201354199 | in-del | -/GGGCG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962771 | ACAAGAGCAAGGTGT[-/GGGCG]GGGCGGGGGGGGGGG | 11252 |
| rs201358924 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871320 | GAGGCTCCTGGGCCC[A/G]CCGCCTCCGTCCCCC | 11252 |
| rs201372955 | snp | C/T | 0.000149151 | 0.00863442 | missense | PACSIN2 | GRCh38.p7 | 22:42882224 | ATGCCCGGCCCGTGA[C/T]TGGCTCGGAACCACC | 11252 |
| rs201415259 | in-del | -/CC/CCAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987493 | CACACACACACACAC[-/CC/CCAT]CCATGGCACCATGTT | 11252 |
| rs201425615 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967115 | GTGCTCCGTAACAGA[A/C]ACTAGGCAGGGAATG | 11252 |
| rs201454696 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982894 | AAAAAAAAAAAACAA[-/C]AACAAGGCTAGGAGC | 11252 |
| rs201534510 | snp | A/G | 3.43371e-05 | 0.00414335 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893447 | CAGGACCTGTGCCGG[A/G]GCCCCATACCTTTCT | 11252 |
| rs201562774 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913990 | AACAGAGACAAAGTC[A/C]ACAACAGATAACGGT | 11252 |
| rs201584184 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948892 | TTCACATAAAATGAA[A/G]TAGCCAGTAATTTGG | 11252 |
| rs201639218 | in-del | -/A | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873369 | GCTTAAAGGCACATT[-/A]AAAAAAAAATCCAAA | 11252 |
| rs201678639 | snp | A/G | 0.000182229 | 0.00954366 | missense | PACSIN2 | GRCh38.p7 | 22:42876277 | GAGAAGGGGTTGTTA[A/G]ACTCATCGTCTGACC | 11252 |
| rs201691749 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42981043 | TAGGAAGCGAGGAGC[A/G]CCTCTTCCCCGCCGC | 11252 |
| rs201696732 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990148 | AATGAATGATTTTTT[A/T]AAAAAGAATGATTTT | 11252 |
| rs201704843 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42981308 | ACCCCGTCTGGGAAG[C/T]GAGGAGCGTCTCCGC | 11252 |
| rs201737132 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921983 | AACTCAGGTGATCCA[C/T]CTGCCTCAGCCTCCC | 11252 |
| rs201782418 | in-del | -/G | 0.0452528 | 0.143452 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911156 | AGATCCACCCGCCTC[-/G]GCCTCCCAAAGTGCT | 11252 |
| rs201893515 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926673 | TCTTCTTCCCACAGG[A/G]AAAAAAAAAAAATCA | 11252 |
| rs201923809 | in-del | -/CCA | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888544 | TATTTATCCCTCTAT[-/CCA]CCACCCATTCACCCA | 11252 |
| rs201932317 | in-del | -/AAAAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913481 | CGAAACTCCGTCTCC[-/AAAAAA]AAAAAAAAAAAAAAA | 11252 |
| rs201945032 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932330 | CTAGCCACACCTCCC[A/C]CCACCACCAACTCTA | 11252 |
| rs201948306 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990830 | GCCATGGAAACCACT[C/G]TATTTGGCTCAAGAG | 11252 |
| rs201951079 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887933 | GCCACCCCTGGCTCC[G/T]CAGCCTCTGCCTCAC | 11252 |
| rs202004264 | in-del | -/GG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974787 | AAAAGAGAAGAAGGA[-/GG]AGGAGGAGGAGGAGA | 11252 |
| rs202019620 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973428 | ATCTGTACCACACTG[G/T]TTTTTGTCAACAAGG | 11252 |
| rs202079767 | snp | C/T | | | missense | PACSIN2 | GRCh38.p7 | 22:42884500 | ACCTGCTCCATGTTC[C/T]CCATGTACTGGGGTG | 11252 |
| rs202095988 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941218 | TCCACGTTGCAGCAT[C/G]TGTATTTCACTCCTT | 11252 |
| rs202119781 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974302 | CCCATGAGCACCAAA[C/T]AGCAGGTGCCATACC | 11252 |
| rs202129205 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917632 | AAAAACCAACCAAAC[A/C]AAAAAAAAAGTGAAC | 11252 |
| rs202136600 | snp | A/G | 0.00160938 | 0.0283214 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879110 | CGTCAGGGTGACGCC[A/G]TCAGTGGCCTTCTTC | 11252 |
| rs202149798 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930319 | GCTCTCTGCCCCAAT[C/T]CCACAGCCACAACAT | 11252 |
| rs202152310 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921372 | TCAAAAAAGAAAAAA[A/G]AAAAAAAAAAAAAAA | 11252 |
| rs202179063 | in-del | -/AT | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990060 | TATATATACACACAC[-/AT]ATGTGTGTATATATA | 11252 |
| rs202216498 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009009 | AGCCTTTTCACATAC[-/A]GAAAAGGTGTTTAGT | 11252 |
| rs202239476 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880823 | CACTGTGCCCCTCTT[A/C]GGGTATAATGGGCAC | 11252 |
| rs202247098 | snp | A/C/T | 0.00572914 | 0.0532148 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877057 | AGCTCTGCAGGGGCC[A/C/T]GTGAGGGTCCTGGCA | 11252 |
| rs367555600 | snp | A/C/T | 0.000115913 | 0.00761212 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876974 | GCTGGACTGTGACTG[A/C/T]GCAGACTGGGCGGGG | 11252 |
| rs367591686 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900676 | ACAGGTTCTTACTAT[A/G]TTGCCAGGGCTGATT | 11252 |
| rs367627262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907538 | CGAGGAGCCCATGGA[A/T]GTGGGCACAGTGCTC | 11252 |
| rs367636532 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875849 | GCCTAATTTTTTGTA[C/G/T]TTTTTGTAGAGACAG | 11252 |
| rs367639439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005780 | CACCTCATGCTGCCC[C/T]GCCAAAATCCTATGA | 11252 |
| rs367641115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902338 | CTGCTGCCCCAGGAC[A/G]CTTCCCCCACAGATT | 11252 |
| rs367657177 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977996 | TACATTGCTAGTACA[A/C]GTCTGAAAAAGACTA | 11252 |
| rs367662679 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915604 | GTTCATCTTAATGCT[C/G]AGCCAGCTCCTCCCT | 11252 |
| rs367665393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997975 | GTTAGGTGAGCAAGG[C/T]AGTAAAATTACAGAG | 11252 |
| rs367736003 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975795 | GCTCCCAGGCATTTA[C/T]TAGTATGTTCCAAAA | 11252 |
| rs367753416 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968164 | GTGTGTCCTGGACCT[A/C]CACAAACAGCGTGAC | 11252 |
| rs367767535 | snp | A/G | 0.000182253 | 0.00954429 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912036 | CTCCCAGAAGCTGTC[A/G]CTGGACACTTCTACT | 11252 |
| rs367779724 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004533 | GAACCCACTAATAGC[A/G]GGCTTGGACGTCTGT | 11252 |
| rs367781234 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986750 | CAGGAAGTGGGAACC[C/G]CACGTGCAAAGACCC | 11252 |
| rs367809915 | snp | A/G | 6.71254e-05 | 0.00579294 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879186 | TAGGCAACAGGTGCC[A/G]AGGGAGAGAAACCAA | 11252 |
| rs367825376 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965100 | AAAACCACTCGGCAA[A/T]AAAAAGGAATGAGCT | 11252 |
| rs367841696 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935686 | AAAGTGTTTCCACAG[A/G]GACAAGGGCAACTTG | 11252 |
| rs367868927 | snp | A/C | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959627 | ATTGCTCAGTTAATA[A/C]TGAACTAATTGAACA | 11252 |
| rs367876498 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948642 | CAACACAGTGAGATC[C/T]CATCTCTAAAAAAAA | 11252 |
| rs367885702 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002373 | TTGGGAACGTGGAAC[A/C]TTAGCTCCAAGGATT | 11252 |
| rs367916321 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908774 | TCAGGCTCCAGACTT[A/G]GTTCCAACCTGGAAT | 11252 |
| rs368074486 | snp | A/G | 6.62943e-05 | 0.00575698 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42890992 | TGCCTTCCGAAAGCC[A/G]TCCTCAGCTTCCTTG | 11252 |
| rs368139995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953442 | TTGCATTGAAGGGCC[C/T]AGCCACTGCAATAAG | 11252 |
| rs368146182 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934244 | TAAATTCAAAACATA[C/T]AACCGAGGCCCAGAG | 11252 |
| rs368151275 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911433 | AAAAAAAAAAGATGG[A/C]CTTTCCATTAACTAG | 11252 |
| rs368177357 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924588 | ACTTTGTCCTCAGAC[C/T]CTGCTCTCCAACCCG | 11252 |
| rs368218313 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912660 | CTAAATGGATCACTT[C/T]TGAATAACAGACTCA | 11252 |
| rs368232425 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985564 | ACTGCCTCCAGCCCT[C/T]GCTCGGCCAACCCCT | 11252 |
| rs368254041 | in-del | -/CAGGGCCCCGGCC | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871849 | CTTCTGTCCCCTCCC[-/CAGGGCCCCGGCC]GCCTTGCTCCCAGCA | 11252 |
| rs368258593 | snp | A/G | 8.28288e-05 | 0.00643487 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876249 | ATTCGAGTCCCCATT[A/G]GCATCCGTGGAGGAG | 11252 |
| rs368286642 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009235 | GTTTGCTCCATCAAC[A/G]TGCTGACCAAGCCTG | 11252 |
| rs368304502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912313 | AGCCAGTAGACTCTA[A/C]TCAACTCTGGGCACA | 11252 |
| rs368328219 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972340 | ATCACCACTCCCTAA[G/T]CTCCAGTACCCAGGG | 11252 |
| rs368378284 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941414 | GTAGATACCTAGGAG[G/T]AGAACTGCTGGGTCA | 11252 |
| rs368396699 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891609 | GTTTCACCATGTTGG[C/T]CAGGCTGGCTGATCT | 11252 |
| rs368401904 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942496 | CACTTATTATGACTA[A/T]TTTTTTTAAACGTTT | 11252 |
| rs368402841 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909251 | CTCCAAATGTCACAG[C/G]CAAAGGCTCCTGGAG | 11252 |
| rs368404162 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982110 | CCGGCCAGCCGCCCC[A/G]TCCGGGAGGGAGGTG | 11252 |
| rs368440149 | snp | A/G | 8.29993e-05 | 0.00644149 | missense, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871367 | ACTCATCACTGGATC[A/G]CCTCCACATAATTTG | 11252 |
| rs368453831 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975880 | ATTTCTAAACTAGGG[-/G]TAGATGAGAGAAATG | 11252 |
| rs368479024 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912649 | CAGCTGGAAAGCTAA[A/C]TGGATCACTTCTGAA | 11252 |
| rs368490307 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899466 | ACCTCTGTATGTGGG[C/T]GCCCAGAGGGATGTG | 11252 |
| rs368514545 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933647 | TCCACACAGATGACA[C/G/T]AGGTCCACCCACTCA | 11252 |
| rs368538184 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971787 | CCGGCCAGCCGCCCC[A/G]TCCGGGAGGGAGGTG | 11252 |
| rs368539596 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007971 | AAAAAGCAGGTACTT[A/C]CACGGGCAGCTTAAT | 11252 |
| rs368541760 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000172 | AAAACATGCCAGAGG[C/T]TTCTCCCTGAACCTC | 11252 |
| rs368570140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880456 | GGATCAACACCAAGC[C/T]GGCACTGATGGGAAG | 11252 |
| rs368570679 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999367 | TGTGTGTGTACGGAG[A/G]CATTAAAAAATCTGT | 11252 |
| rs368601536 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982782 | CCAGAGACCTTTGTT[C/T]ACTTGTTTATCTGCT | 11252 |
| rs368619895 | snp | C/T | 6.83784e-05 | 0.00584675 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879037 | TTTGGATGGAGGTGG[C/T]GCCCACTCACCTGCT | 11252 |
| rs368628142 | snp | A/G | 6.64341e-05 | 0.00576304 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888605 | GTCAACAACTGACAC[A/G]GTGACACTCGACGTG | 11252 |
| rs368670934 | snp | C/G/T | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936330 | ATACCTGTCTCTCAT[C/G/T]TGGCAAACAATCCAT | 11252 |
| rs368703889 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990426 | TGCAGTCCCCTGCCC[C/T]CCGCCTACCCAGCTC | 11252 |
| rs368710509 | snp | C/T | 0.00010003 | 0.00707142 | synonymous-codon, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893527 | CGCCTTCTCGATGCG[C/T]GCCCGCTCATGCAGG | 11252 |
| rs368737642 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919049 | CATACCTGTGCACAC[A/G]TATGGGACAAGCTGC | 11252 |
| rs368772370 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008090 | CATTGAGTGATGCCT[A/G]CTGTGTGCAGTACTA | 11252 |
| rs368786654 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996206 | GGCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 11252 |
| rs368792492 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935081 | CCACCGCGCCCGGCT[A/T]ATTTTTTTTTTTTTT | 11252 |
| rs368797833 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910146 | CCTCCTGGCTCCAAA[G/T]CAATGTCTTCACCTG | 11252 |
| rs368841124 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992852 | GAAGCCAGACTAAAA[A/G]TAACACATACTGTAA | 11252 |
| rs368848384 | snp | A/G | 6.7555e-05 | 0.00581145 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871337 | CGCCTCCGTCCCCCC[A/G]CTGGCCTGTCCCCGA | 11252 |
| rs368857255 | snp | A/G | 3.45405e-05 | 0.00415561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893426 | GGTGTAGCTGCCTCC[A/G]GGCCACAGGACCTGT | 11252 |
| rs368876422 | snp | A/G | 1.66499e-05 | 0.00288525 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884394 | AACTTACCCAGCCAC[A/G]TTGGACAGGTCTAGG | 11252 |
| rs368896713 | snp | A/G | 1.66338e-05 | 0.00288386 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879074 | ACTCGGCAGAGACTG[A/G]TCGCCTGTCTGGTTG | 11252 |
| rs368914363 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938604 | AGAATGCCTCTGCAC[A/T]GGCCAACTGCATGTT | 11252 |
| rs368916881 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977372 | AACGGAGAAAGGATA[C/G/T]AGGTATGGAATTCAC | 11252 |
| rs369002558 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950987 | CAGAGAGTGACAGGG[C/T]CTACCTGGACATATG | 11252 |
| rs369014935 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960487 | AAGAACTAGGACACT[C/G]AAATACGCAACTGTG | 11252 |
| rs369036329 | snp | A/G | 6.62636e-05 | 0.00575564 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876270 | CGTGGAGGAGAAGGG[A/G]TTGTTAGACTCATCG | 11252 |
| rs369051515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917056 | TACCCACCCCTATGG[C/T]GACTCCTCATGTGCC | 11252 |
| rs369055884 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915994 | GAGTCAGTGACGTAA[G/T]GCAGACGAGGTGCCT | 11252 |
| rs369062100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942694 | TGAACTGGCTTAGCA[C/T]CCTTGTCCAAAGTCA | 11252 |
| rs369080510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885165 | TAAAAAGCAGGTGTG[A/G]CCTATCTCAAGAATA | 11252 |
| rs369148435 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987912 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG | 11252 |
| rs369183239 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985663 | CAACAGACACACACA[-/CA]GACACATTCACATGT | 11252 |
| rs369188422 | snp | C/T | 0.000159987 | 0.00894249 | missense | PACSIN2 | GRCh38.p7 | 22:42882267 | CTGCATCAGCTGCTC[C/T]GATGCTCTGCTCCAG | 11252 |
| rs369224478 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903013 | AGTAACTTCATGGCC[A/G]GCAGAAGAGCAACTC | 11252 |
| rs369258869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940616 | GCTGGAGAGGGGCCA[A/C]CCCAGGTCCTGGGTT | 11252 |
| rs369262722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968689 | ATCAATAAGGGCAGG[C/T]ACCATCCAATCTGCC | 11252 |
| rs369290090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904593 | AAACTGGCTCGACCC[C/G]TAAGGTCCAAAGCCG | 11252 |
| rs369301054 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870614 | ACAGTTTTAAGCAAG[A/G]ATAGAGTGAAAATAA | 11252 |
| rs369321222 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891695 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCATGCC | 11252 |
| rs369324754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906055 | AGGGGACAGTGGCCA[C/T]GGACAGGGATGGCAG | 11252 |
| rs369333766 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974259 | CCACCAAGGGCCTGG[C/T]GCCTGAACCGTCTAC | 11252 |
| rs369338813 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016367 | AGAAACAAAAGAACC[A/G]GCTAGGCACGGTGGC | 11252 |
| rs369339746 | snp | G/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896080 | ACACTTAGATCTGAA[G/T]GTGGACAAACATATA | 11252 |
| rs369341550 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954811 | TGGGGGATGGGGGCA[G/T]GGATTCAAAGTCTCA | 11252 |
| rs369386748 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936918 | TCTGCCTCAAAAAAA[-/G]GGGGGGGGGCAGGGG | 11252 |
| rs369426411 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960686 | CTAATCTACACCCTT[C/T]GAAGCCGGGACAGGG | 11252 |
| rs369451109 | snp | C/T | 6.6313e-05 | 0.00575779 | missense | PACSIN2 | GRCh38.p7 | 22:42876296 | CATCGTCTGACCAGT[C/T]GGTGGGATAGCTCTG | 11252 |
| rs369474399 | snp | C/G | 0.000307953 | 0.0124049 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884356 | CGTTGACTTCAATGA[C/G]GTGTGTGTTTTAGCT | 11252 |
| rs369499371 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004085 | AATTATCTTTTAAAG[A/T]TGTTCACATCTGAGA | 11252 |
| rs369519345 | snp | A/G | 1.66515e-05 | 0.00288539 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893594 | TCGATCCGCTTCACA[A/G]TCCGCTTGTAGTTCC | 11252 |
| rs369521673 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921321 | CCGAGATTGTGTCAC[G/T]GTCGCCCACCCTGGG | 11252 |
| rs369532636 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987608 | GCAATCTCGGCTCAC[C/T]GCAACCTCCGCCTCC | 11252 |
| rs369544015 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898202 | TCCCTGGCTCCCAGA[C/T]AGGTTTCTCTGCATA | 11252 |
| rs369567023 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964405 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTGGAA | 11252 |
| rs369600317 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913202 | AAGAGACAATAGGCC[A/G]GGCACAGTGGCTCAT | 11252 |
| rs369604606 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880987 | GAGAGGCTGGGCTTT[A/G]TGCTGTCCCCTCTAG | 11252 |
| rs369642605 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881307 | AACAGCCCCCGACAG[G/T]AGATGGGTGCTCTTG | 11252 |
| rs369656984 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913464 | AGCCTGGGCAACAAG[A/T]GCGAAACTCCGTCTC | 11252 |
| rs369679702 | snp | A/T | 0.418974 | 0.184249 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014324 | CTCCCCCCGCCCTAC[A/T]CACACACACACACAC | 11252 |
| rs369699773 | snp | G/T | 9.97108e-05 | 0.00706013 | missense | PACSIN2 | GRCh38.p7 | 22:42879087 | TGGTCGCCTGTCTGG[G/T]TGATGCCCGTCAGGG | 11252 |
| rs369706993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949457 | AGCCTCATACACACA[C/T]GCGCGCGCACGCACA | 11252 |
| rs369726351 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917649 | AAAAAAAAGTGAACA[C/T]GCACTGCTCTGCGGT | 11252 |
| rs369727314 | snp | A/G/T | 4.94828e-05 | 0.00497387 | missense | PACSIN2 | GRCh38.p7 | 22:42884453 | GGAAGAAGCGAAGGC[A/G/T]TTTCTCCTCGAACTG | 11252 |
| rs369775632 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935156 | GGTCTCGATCTCCTG[A/T]CCTCATGATCTGCCC | 11252 |
| rs369789754 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001564 | CAGTCAGACGAGCCC[C/T]GAAGTGTGGGCACAA | 11252 |
| rs369795010 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886464 | TAGGTATGTATGTAC[C/G]TACCTACTTACCTAC | 11252 |
| rs369815873 | in-del | -/GAAAAGA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943788 | ATTCTCTGGCTTTGA[-/GAAAAGA]AATTTGTGATAATAA | 11252 |
| rs369817122 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004867 | GCAGGTGGCCTCAGG[-/C]AAAACCACTCACCCC | 11252 |
| rs369846921 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871146 | TATTTCTGTTGTTCT[A/G]CGTCTTCCTGCGCTC | 11252 |
| rs369879289 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973705 | TGGCTGCTCTCCCCT[G/T]TAACTGACACAGAAA | 11252 |
| rs369900647 | snp | C/G | 0.00148066 | 0.0271686 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891154 | CATGAAGGCCATCCA[C/G]GCCTTCTCCACGGTC | 11252 |
| rs369916486 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984631 | ACTACTCCCTTTAAT[C/G]GGTGCTTCAGGGCAT | 11252 |
| rs369931296 | snp | C/T | 1.6607e-05 | 0.00288153 | missense | PACSIN2 | GRCh38.p7 | 22:42879108 | CCCGTCAGGGTGACG[C/T]CGTCAGTGGCCTTCT | 11252 |
| rs369963580 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999363 | TGTATGTGTGTGTAC[A/G]GAGGCATTAAAAAAT | 11252 |
| rs369964899 | snp | C/T | 1.65444e-05 | 0.00287609 | missense | PACSIN2 | GRCh38.p7 | 22:42884420 | CTAGGTGCTTCTGAA[C/T]CTCCAGCAGAACCTC | 11252 |
| rs370050109 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012846 | TTTAGTAGACATGGG[G/T]TTTCTCCATGTTGGT | 11252 |
| rs370059379 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954173 | GAGGCTGAGGCAAGA[A/G]AATCACTTGAACCTG | 11252 |
| rs370082819 | in-del | -/GAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988234 | GGCACCAAAGACAAG[-/GAG]AAGATAGTCTCTGAA | 11252 |
| rs370127212 | snp | A/G | 0.000166069 | 0.00911081 | missense | PACSIN2 | GRCh38.p7 | 22:42879136 | TCTTCTTCTCTCTCC[A/G]GCTGAGGGTTCGATT | 11252 |
| rs370132657 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891445 | CGCTCTTATTGTCCC[A/G]GCTGGAGTGCAGAGA | 11252 |
| rs370175249 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956231 | TCAAATTAATTCTAA[C/T]TTCCTATTAGATTCT | 11252 |
| rs370178300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921984 | ACTCAGGTGATCCAC[C/T]TGCCTCAGCCTCCCA | 11252 |
| rs370192258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926798 | GATCACGCCTGTGAA[C/T]AGCCACTGCACTCCT | 11252 |
| rs370192995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994788 | GGGAATGCTGACATA[G/T]GAAAGGTCTGGGGGC | 11252 |
| rs370197986 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963912 | TGCCTTAAAAAAAAA[-/A]CAGCTTTATTGAGAT | 11252 |
| rs370217179 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885823 | GGGCTTGGGTCCTCT[A/G]TGCCAGGAAAAGGCC | 11252 |
| rs370253190 | snp | C/G/T | 3.29708e-05 | 0.00406011 | missense | PACSIN2 | GRCh38.p7 | 22:42884509 | ATGTTCTCCATGTAC[C/G/T]GGGGTGTGCCCTGGT | 11252 |
| rs370269064 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880351 | TGACCAAAATAGATT[-/T]GACTGAGAACTCAAT | 11252 |
| rs370271178 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897687 | CGGAGGGCCAAGCAT[A/G]TACCTACTGAGGGAC | 11252 |
| rs370281121 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946394 | GGAAGGAGGCACACA[G/T]TGGCCTCTGAGCCTG | 11252 |
| rs370328103 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961612 | CCTCATCTCTACTAA[A/T]AAATACAAAAATTGG | 11252 |
| rs370334558 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990681 | GGCAAGAGATGAGAC[A/T]CAACGGGTAAGCAGG | 11252 |
| rs370367716 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946664 | GCAGTGTTATTCCAA[C/T]ATAATCTTAGGATCC | 11252 |
| rs370417006 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917773 | TCTGCATTTCCCTCA[C/T]TGATTGGTACTCTTT | 11252 |
| rs370426951 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887023 | TCTTTCCTCTAGGCA[A/C]CTTTTTGGGCACCTG | 11252 |
| rs370434692 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951258 | AACCGGCCTGCAGTA[C/T]TAACTGCATTCTCTC | 11252 |
| rs370438215 | snp | A/G | 0.000248346 | 0.0111405 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876920 | GTCCTTCTCACTGAC[A/G]GTGCTGCCCGTGTCG | 11252 |
| rs370440070 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942301 | GAAACTATTTTCTTC[C/T]ATTCTGAGTTGTCTT | 11252 |
| rs370444545 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971053 | GCTAAGCTAAAAACA[A/G]TGAAAGGAGGTGGCA | 11252 |
| rs370482570 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879756 | TGCAAATAAAACCAG[A/G]TGCAAATAAAGCCAC | 11252 |
| rs370488998 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903213 | TCCCTTCTCCTCAGG[A/G]CTGTGCCCTGCAGAG | 11252 |
| rs370498277 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886118 | CAACAAGATGCTCCA[C/T]CTCTGGGCTGCCCCT | 11252 |
| rs370500908 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912208 | AATTCCCAAGGTAAA[G/T]AAACAAGTCATCTCT | 11252 |
| rs370539017 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971873 | CCCCGCCCAGCCAGC[A/C]GCCCCGTTCGGGAGG | 11252 |
| rs370546447 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963005 | GCTGCCCGACCACTC[C/T]TTAGGTGATGCTGGG | 11252 |
| rs370588886 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014978 | CGTCCCGCCCGCGGC[G/T]CCCCAACCGTCGCGG | 11252 |
| rs370590166 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009088 | AGTTTCCTCTACGAG[G/T]GACACATTCTGGGAT | 11252 |
| rs370596304 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003248 | GAACCTTCAATTTTT[-/A]AAAAGATTTAAAGAA | 11252 |
| rs370599916 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927902 | TCAGTCATTTTTAAT[A/G]GCTGTAAAACGTCAT | 11252 |
| rs370654851 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990070 | CACACATATGTGTGT[A/G]TATATATGTGTGTGT | 11252 |
| rs370659754 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962152 | AAAAATTGTCTACCT[C/G]TTCCCTCCCCCAAGC | 11252 |
| rs370671698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007768 | CTGAGCTGCCTTTAC[A/G]GAGCAGCCATCATCT | 11252 |
| rs370675525 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890164 | CCGCCACCACGCCCT[A/G]CTAATTTTTGTACTT | 11252 |
| rs370683801 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872002 | CCTGGCTGATGACTT[A/G]TGCACGGTGCCATGT | 11252 |
| rs370762852 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901833 | CTGGGTCAGACATTC[A/C/G]ACTCTGGTTCCATGG | 11252 |
| rs370772133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968161 | CGAGTGTGTCCTGGA[C/T]CTCCACAAACAGCGT | 11252 |
| rs370772325 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974642 | TAATCCCAGCTACTC[A/G]GGTGGCTGAGGCACC | 11252 |
| rs370775161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931922 | AAAACGTTTAATGTT[C/T]TCCCATGGAAACTCA | 11252 |
| rs370781483 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967806 | GGCAGGAGAATGGCA[C/T]GAACCCGGGAGGCAG | 11252 |
| rs370816929 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956648 | AAGGTTCTGAGGCCA[C/G]TTCTAGAATCTGGTC | 11252 |
| rs370826871 | snp | A/G | 0.000214601 | 0.0103564 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884526 | GGGTGTGCCCTGGTC[A/G]AGTTCCTTCAGGGAC | 11252 |
| rs370854467 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014339 | ACACACACACACACA[C/G]ACACACACACACAGA | 11252 |
| rs370877230 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892294 | GACAGTGACCAAGTG[C/T]GCTGAGTCATGACAG | 11252 |
| rs370884826 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914226 | CCTGGGCCCTGATGC[C/T]ACCTCTCACAGTAAT | 11252 |
| rs370886049 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871128 | TGGGCGGGGAGGGGC[A/G]GCTATTTCTGTTGTT | 11252 |
| rs370977177 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919651 | GGTAGCATGCGCCTG[C/T]AATCTCAGCTACTCA | 11252 |
| rs370978536 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885583 | CAGCTGGGACTGAGT[C/T]TACCCTGCCCATGCG | 11252 |
| rs370988024 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004086 | ATTATCTTTTAAAGA[C/T]GTTCACATCTGAGAG | 11252 |
| rs371037013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011628 | GAAACAAAAGGCAAG[A/G]ACATCTGCGAGGCCG | 11252 |
| rs371129736 | snp | G/T | 0.000281678 | 0.0118642 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912001 | CCACTTCATTCACTG[G/T]AAGAAAGCAGGTGCA | 11252 |
| rs371183720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008730 | TTCAAACCCACCCAG[C/T]GGCTCTGGGCCCAGG | 11252 |
| rs371199683 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960822 | TATGTACACTTGAGA[A/T]CTGTGCACTTTAGGT | 11252 |
| rs371256182 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004703 | TGGGTATCACTTTAC[A/G]TTAAGAAGATTTCAT | 11252 |
| rs371287701 | snp | C/G | 1.66582e-05 | 0.00288597 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871501 | GAGCCGTCTCCATGA[C/G]AGGTATGACACCGAC | 11252 |
| rs371324876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003516 | GCTGAGGCAGGAGAA[C/T]GGTGTGAACCCAGGA | 11252 |
| rs371373906 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935218 | GCGTGAGCCACCGTG[C/G]CCAGCCCAGGGCATG | 11252 |
| rs371387144 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901089 | TTGCCAAGGATGACC[C/T]TGATTTTAACCTCAG | 11252 |
| rs371422883 | snp | A/C/T | 0.000199761 | 0.00999237 | missense | PACSIN2 | GRCh38.p7 | 22:42884395 | ACTTACCCAGCCACA[A/C/T]TGGACAGGTCTAGGT | 11252 |
| rs371436335 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870455 | ACGAGTGCTTTAGAT[-/T]CTCTGAATATCAAAT | 11252 |
| rs371445231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926229 | CGGGAAACAGCTTGC[A/G]CATTGCAAGATGCTT | 11252 |
| rs371459196 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000128 | CTGCAGGCACTTGTA[A/G]CCCCAATGGACGGGG | 11252 |
| rs371459358 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983033 | TAAAAATACAAAAAT[C/T]AGGCCGGGCACAGTG | 11252 |
| rs371492318 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883577 | CACAATTCAGAACCA[A/G]GTCTCAGAGGGTATG | 11252 |
| rs371512988 | snp | A/C/G | 0.0107236 | 0.0724357 | missense | PACSIN2 | GRCh38.p7 | 22:42884389 | AAGGAAACTTACCCA[A/C/G]CCACATTGGACAGGT | 11252 |
| rs371606498 | in-del | -/CTTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917807 | TTTCTTTTTCTTTTT[-/CTTTTT]AGAGATGGGATCTCA | 11252 |
| rs371656133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986754 | AAGTGGGAACCCCAC[A/G]TGCAAAGACCCTAAG | 11252 |
| rs371661122 | snp | C/T | 0.000803751 | 0.0200307 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871513 | TGAGAGGTATGACAC[C/T]GACGGTGGGCTACAG | 11252 |
| rs371664696 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944012 | GAAGAGGAGATGGCT[A/G]GGCAGAGACAGGAAT | 11252 |
| rs371714947 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915738 | GCACAAGGCATTTCA[G/T]ACCCAACAGAAATTA | 11252 |
| rs371718103 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948189 | TCCTGGAGGGCAAAC[C/G]CTGGGAAGCTGCTGT | 11252 |
| rs371742266 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983559 | ATGCAAAAAAAATAA[C/G]CAGCAGTTCTAATTA | 11252 |
| rs371799215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986766 | CACGTGCAAAGACCC[C/T]AAGAAGGGGCAGCAG | 11252 |
| rs371816726 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012023 | GGTGGTGGATGCCTG[G/T]AGTCCCAGTTACTCA | 11252 |
| rs371819620 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912723 | CAATTATTTCCCCTG[C/T]TGGAGGGAAGAAACT | 11252 |
| rs371858029 | in-del | -/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979965 | CATACAATACACATA[-/TA]GTATAAATACACATA | 11252 |
| rs371865681 | snp | A/T | 0.0002185 | 0.01045 | missense | PACSIN2 | GRCh38.p7 | 22:42882291 | GCTCCAGGTCATGGT[A/T]AATGGCTTTGTAGCT | 11252 |
| rs371873637 | snp | C/T | 0.000225422 | 0.0106142 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879004 | ATTGCCCAGGGCCCC[C/T]ACCATGGAACGGCCT | 11252 |
| rs371914746 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935065 | GGACTACAGGTGCCC[A/G]CCACCGCGCCCGGCT | 11252 |
| rs371930993 | snp | A/T | 0.000348545 | 0.0131966 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888611 | AACTGACACGGTGAC[A/T]CTCGACGTGTAAAAA | 11252 |
| rs371986948 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968533 | TCATGGTTAGTTTTA[C/G]AGTTTTAGGTGTCAA | 11252 |
| rs371989743 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920030 | GGAGGATCACTTGAG[C/T]CCAGGAGCTGGAGGC | 11252 |
| rs372001621 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910526 | AAGGCAGTCCTGAAT[C/T]CTAGCACTATTCCAG | 11252 |
| rs372042795 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950421 | GGGAGGGAGGGAAGG[-/A]GAGTGGGCAGGTGGG | 11252 |
| rs372078900 | snp | A/G | 1.69238e-05 | 0.00290888 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879042 | ATGGAGGTGGCGCCC[A/G]CTCACCTGCTGGGCT | 11252 |
| rs372110284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959718 | TCAGTCACTCAGTGA[G/T]AAAGAAAACAATTCC | 11252 |
| rs372138986 | snp | A/G | 3.31318e-05 | 0.00406999 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876225 | CGAGGTGGCGTCGTC[A/G]TCGAATGGATTCGAG | 11252 |
| rs372153807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904422 | TGCTCTCCCTCACTC[C/T]TCAGGGAGGCGCCCC | 11252 |
| rs372171455 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910417 | GCTGCTGCCAGCTCC[A/G]TAAGCGCTCCTGCAC | 11252 |
| rs372179686 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986572 | GCTGCTGAGTGCACA[G/T]GCATGACAGTGACAC | 11252 |
| rs372184147 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003987 | TGAAACCAAGTTAGT[C/T]ACAGACATAGATGCC | 11252 |
| rs372200654 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957856 | TTCTCATCTGGCAAG[C/T]AATCCCATCGTGAGG | 11252 |
| rs372211838 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893832 | GTGAACGGGGGCTTC[C/T]CAATGTTCTTTAGGT | 11252 |
| rs372238878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973069 | TGACAGGGCAGTCAT[A/G]TATCTGCCCACATAC | 11252 |
| rs372252356 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009470 | ATCCAGTTCTTAATC[C/T]GGGTCCACGCCTATG | 11252 |
| rs372271560 | snp | C/T | 1.66272e-05 | 0.00288328 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893556 | GGCAGTTCATGAGGT[C/T]GCTGCACAGGCGGTG | 11252 |
| rs372279770 | snp | A/G | 4.96981e-05 | 0.00498463 | missense | PACSIN2 | GRCh38.p7 | 22:42876256 | TCCCCATTGGCATCC[A/G]TGGAGGAGAAGGGGT | 11252 |
| rs372283631 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953820 | ATAAACATATATGTG[C/T]CCTCTCAGAGGCAAG | 11252 |
| rs372287174 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915417 | ATACTTATTCACTTT[C/T]CTTCTGTCTGGGACC | 11252 |
| rs372289595 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015540 | CTACAGTCTTTCAGA[A/C]AGTTTCCTCTCCCAA | 11252 |
| rs372303632 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933163 | GGAAAACCTTGTTAT[C/T]CCTGAAAAGTTGAGG | 11252 |
| rs372313821 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953165 | GAGAGGGCATATGGA[A/G]TTAAAATGTTTTCTA | 11252 |
| rs372315696 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917217 | GCAGCGGAGTTGAGA[C/T]CTTAATAAAGGCAGG | 11252 |
| rs372329504 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880269 | ATGTGATTTGCCCAC[A/G]CAGTGTGGGTGGCAG | 11252 |
| rs372361260 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891859 | ACCCACCCACACCAT[A/G]CCAACGCTTCTCCTG | 11252 |
| rs372378193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991115 | ATGAGTCAGAACACA[C/T]TGCCCCCAGATCAAA | 11252 |
| rs372381979 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917334 | AATATCGGTCAGACA[C/T]GGTGGCTCACACCTG | 11252 |
| rs372403207 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884271 | CCCTGAGGGCGGTGA[A/G]GAGACCTCCTGATGA | 11252 |
| rs372418841 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941854 | CATTCTCGGCTCACT[C/G]CAACCTCTGACTCCT | 11252 |
| rs372421267 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978427 | AAAATATCAGTCTTC[G/T]TTTACACGCAACACA | 11252 |
| rs372437253 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870076 | CCCGCGTAACTCTGG[C/T]TGCAGCACCTGCTCC | 11252 |
| rs372446992 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876418 | AGGGGAGGGCACTGG[A/G]GCCTTGGGGCTCAGG | 11252 |
| rs372473749 | snp | C/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938437 | AGAAAGAAGCCTGAC[C/G/T]TTCTCCCTTTCCCAT | 11252 |
| rs372491299 | snp | A/G | 1.65677e-05 | 0.00287812 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876276 | GGAGAAGGGGTTGTT[A/G]GACTCATCGTCTGAC | 11252 |
| rs372523168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930533 | GGAAAAAGTTATTCA[A/G]TAAACTAATTTTGAA | 11252 |
| rs372533042 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42949070 | GGTGGAGGTGGAAGG[A/G]TTGCTTGAGCCCAGG | 11252 |
| rs372536834 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916046 | GGAAGGCGGGAAATC[C/T]GAGCTCTACCACTGG | 11252 |
| rs372543407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968705 | ACCATCCAATCTGCC[A/G]GGGGCCTAAAAAGAA | 11252 |
| rs372545054 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872895 | GATGAACCACCATCT[C/T]TTTCCACCGCTTCGT | 11252 |
| rs372547955 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891646 | CCTGACCTCAGGTGA[A/T]CCATTCGCCTCGGCC | 11252 |
| rs372574168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887333 | GGCATATGTATGGGC[C/T]TGAGGTCAGAAGTTC | 11252 |
| rs372575755 | snp | C/G | 0.114387 | 0.210022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014378 | CACCACCCCCCCCCC[C/G]CCGGGACACGGAGGG | 11252 |
| rs372636914 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920728 | GTAGGAACGCCAAGC[A/T]CAGGGTTGAGAAATG | 11252 |
| rs372652304 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910442 | TGCACTAATGAGGCC[-/A]ACAGCCTCTCTGGGG | 11252 |
| rs372676255 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992005 | CAAGCCGTAAAAGAA[C/T]AAATTGACTTCAGCA | 11252 |
| rs372721869 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929247 | ATGCTTCCCAAGCAC[A/G]TCCACATCACATAAA | 11252 |
| rs372763586 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895602 | TCGGCACACACAGGA[A/G]CTGCAAATACACATT | 11252 |
| rs372780002 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984459 | GTTGATATGTGAACC[C/T]AGTAAAACACTGGTC | 11252 |
| rs372790775 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920993 | TAGAGACGGGGTTTC[A/G]TCGTATTGCCCAAGC | 11252 |
| rs372825075 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892101 | AGGAGGGGCTGAGTC[A/G]CCTCTCCCTACTCAC | 11252 |
| rs372840444 | snp | A/G | 6.62921e-05 | 0.00575688 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882159 | CTTCCAGGCTGATGA[A/G]CTCATGGGCACACCC | 11252 |
| rs372883557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936309 | TCACTTAGATCATGC[A/G]GGGAAATACCTGTCT | 11252 |
| rs372896477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955308 | GAATGAACAAACAAA[C/T]GAACGAACGAACGAA | 11252 |
| rs372918628 | snp | A/G | 8.32106e-05 | 0.00644968 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871351 | CGCTGGCCTGTCCCC[A/G]ACTCATCACTGGATC | 11252 |
| rs372920955 | snp | A/G | 8.59262e-05 | 0.00655406 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893445 | CACAGGACCTGTGCC[A/G]GGGCCCCATACCTTT | 11252 |
| rs372963694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989476 | GCACTCCAGCCTGGG[A/C]AATAAGAGTGAAACT | 11252 |
| rs373006624 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004139 | AGCCAGCCAGAGGAG[A/G]TGAAATGAGTGTGGG | 11252 |
| rs373009879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013463 | GTGAAAGTTTTCCAG[A/G]TGAATCAAGAGAGAT | 11252 |
| rs373030088 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940537 | GTCAGCCAGTTACAC[-/C]AGAAGCAGTGCCACC | 11252 |
| rs373049960 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889916 | CTATCGTCAAAGGGA[-/C]TTGAAAAAAAAATAA | 11252 |
| rs373056318 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908039 | CTCTTCAGGGCTAAC[-/CA]AYTCCCAGAATATTT | 11252 |
| rs373105276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011454 | TGGTAAATGCCACTG[C/T]GAACTCTAAACACAA | 11252 |
| rs373107308 | in-del | A/TCCTGAGCCAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876516 | CATCCTGAGCCATCA[A/TCCTGAGCCAT]CAGGCTTTCCAGGGG | 11252 |
| rs373135430 | snp | C/T | 0.000116016 | 0.00761541 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911989 | CTATTGGCCTGGCCA[C/T]TTCATTCACTGGAAG | 11252 |
| rs373142363 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010604 | AGTCCCAGCTACTTG[G/T]GAGGCTGAGGCAGGA | 11252 |
| rs373143735 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910908 | ACTCAGTTAACACAT[A/C]ATTTTTTTTTTTTTG | 11252 |
| rs373173379 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017491 | CACGAGCCACTGTAC[A/G]CAGCCTCTCCCAAGG | 11252 |
| rs373237666 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007445 | GGTCTCAAACTCCTG[G/T]CCTCAAGTGATCCGC | 11252 |
| rs373261502 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991237 | AAAGAATGAACTTGT[A/G]TTAACCCCTCCCACC | 11252 |
| rs373288518 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874201 | CATCTGTGGTCCCAG[C/T]TACGTAGGAGGCTGA | 11252 |
| rs373296469 | snp | C/T | 0.000117043 | 0.00764905 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871319 | TGAGGCTCCTGGGCC[C/T]GCCGCCTCCGTCCCC | 11252 |
| rs373314026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970238 | CAAGGTTAACATCAC[A/G]GTGGTGAGTCATGGC | 11252 |
| rs373318181 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905856 | TAAAAGCAGGAAGCC[A/G]CCTGTGGGAACCAGG | 11252 |
| rs373345978 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897920 | AGAGAAGTCAGCTGG[G/T]AATGGAACACAGAAC | 11252 |
| rs373358445 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996281 | GCTCACGCCTGTAAT[C/T]CTAGCACTTTGGGAG | 11252 |
| rs373391539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002676 | TCATACCCTTTAATA[C/T]AAGATTTCTATTCTC | 11252 |
| rs373406561 | in-del | -/A | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872449 | TTATTGCTAAGTTTG[-/A]AGTTTTGTAACTCTC | 11252 |
| rs373455963 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966590 | AACAGTGAAGTGAGA[C/T]TAATTAATGGAGACA | 11252 |
| rs373460445 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946011 | CACGCTCTGGCCACC[A/G]TTAATCACCTGTGTC | 11252 |
| rs373497696 | snp | A/G | 0.000280512 | 0.0118396 | missense | PACSIN2 | GRCh38.p7 | 22:42884447 | CCTCCCGGAAGAAGC[A/G]AAGGCGTTTCTCCTC | 11252 |
| rs373516604 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957894 | CTATCAGTAACAATT[C/G]ACTGTCTCTCCCCTG | 11252 |
| rs373520023 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984161 | TTTTTTTGTAGAGAC[A/G]GAGTTTCGCCATGTT | 11252 |
| rs373552992 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879933 | AAGCAAAGCAGAGTA[C/T]GCTCCTCCTGGAAGC | 11252 |
| rs373560391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932168 | TCTGTCCCAGCACAG[G/T]ATCTTCTCTCTGTTT | 11252 |
| rs373572481 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901888 | GGGCGTCTTCCTTCC[A/G]TGGTTCAGCTCGGAC | 11252 |
| rs373580004 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911392 | TCCAGCCTGCGCTCT[C/T]GAGACCTCAACTGTT | 11252 |
| rs373620587 | snp | C/T | 1.65704e-05 | 0.00287836 | missense, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871424 | TCCAAGCGTCCCTTG[C/T]ACCAGCCCTGCTCAT | 11252 |
| rs373653270 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967128 | AGAAACTAGGCAGGG[-/A]ATGTGGAAGGTGGGG | 11252 |
| rs373705215 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872457 | AAGTTTGAAGTTTTG[C/T]AACTCTCTTTGGCAT | 11252 |
| rs373709236 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978819 | GGTCCCTGCCCCTTA[A/G]CTGGTTCCTCCTCCT | 11252 |
| rs373750364 | snp | G/T | 0.0003648 | 0.0135006 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871381 | CGCCTCCACATAATT[G/T]GCCGGGTATAGGCCA | 11252 |
| rs373791665 | snp | A/C | 3.6325e-05 | 0.00426159 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891204 | AGGGGAGAGAAGCTG[A/C]GGGTCACTCAGCGCC | 11252 |
| rs373829945 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967966 | ATGACATTTTATACA[C/T]GCTCCTCAGATCTTT | 11252 |
| rs373844150 | in-del | -/ACACACACAGAGCT/TCAGACACACACACACAGAGCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014380 | CACCCCCCCCCCCCC[lengthTooLong]GGGACACGGAGGGTG | 11252 |
| rs373871578 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931051 | GAATTCTTTCATTCA[C/T]TCATTCATTCGCTCA | 11252 |
| rs373874739 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999313 | GTCCAGGGAACTCTC[A/C]CATTTCAGTAACATA | 11252 |
| rs373885728 | snp | A/G | 0.000248783 | 0.0111503 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877048 | GGGGATCCCAGCTCT[A/G]CAGGGGCCCGTGAGG | 11252 |
| rs373943936 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935611 | TATTCATCAAGTCCT[A/G]TAATCACTGAGATTT | 11252 |
| rs373959797 | snp | C/T | 9.94415e-05 | 0.00705059 | missense | PACSIN2 | GRCh38.p7 | 22:42890991 | GTGCCTTCCGAAAGC[C/T]GTCCTCAGCTTCCTT | 11252 |
| rs373962563 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002166 | CAGGAACCCCCATGA[C/G]AGCAGCATCTAGAAG | 11252 |
| rs373963058 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882858 | GATCACTGCTGGACC[C/T]GATATTTTCACTTAT | 11252 |
| rs373970839 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886542 | GTGACCACAGCTTGC[A/G]GCAGCCTTGAACTCC | 11252 |
| rs373993590 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944826 | ACTGTAGCTGGGCGC[A/G]GTGGCTCACGCCTAT | 11252 |
| rs374026328 | in-del | -/AACCAGCTGGGT | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931251 | CCCAGCCTTGCTGCA[-/AACCAGCTGGGT]AACCAGGGGCACGTT | 11252 |
| rs374033835 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894238 | GTGGCTAGGCTGGAG[A/C]TGAAGGCAATTGTTT | 11252 |
| rs374039568 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914494 | CCCACCTTGCCCTCC[C/T]GAAGTGCTGGGATTA | 11252 |
| rs374042644 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946427 | GAGAGCAGCAATGTA[C/T]CACGGGCTCACCCAC | 11252 |
| rs374062800 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895273 | TCCCTTAAAATGAGG[C/G]CTTACTGTCATTTTG | 11252 |
| rs374064300 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900724 | AGCAATCCTCCCAAC[C/T]TGGACTCCCAAAGTG | 11252 |
| rs374113724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882888 | TAATCTTTATGGCTG[A/G]TGAGTCATGTACTTT | 11252 |
| rs374119889 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897796 | GGGCATCTTCAAGGA[C/T]AGGTAGGAGGCTGGC | 11252 |
| rs374136765 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963429 | GGGCAGCACTTCCCA[A/G]GGGGATTCTTTCGCC | 11252 |
| rs374143383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883734 | GCTGCGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 11252 |
| rs374170987 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901887 | AGGGCGTCTTCCTTC[C/T]GTGGTTCAGCTCGGA | 11252 |
| rs374202921 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963912 | GCCTTAAAAAAAAAA[-/A]CAGCTTTATTGAGAT | 11252 |
| rs374262036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878622 | CCTCCCTCGACTGGC[A/G]CCTGCACACAATACA | 11252 |
| rs374273939 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003560 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 11252 |
| rs374290800 | snp | A/C/G | 4.97651e-05 | 0.00498804 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882148 | GCCCAGGTCCTCTTC[A/C/G]AGGCTGATGAGCTCA | 11252 |
| rs374318095 | in-del | -/ATGTGTGTGTGT | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999339 | ACATATAAATGTCTA[-/ATGTGTGTGTGT]ATGTGTGTGTACGGA | 11252 |
| rs374333325 | snp | C/T | 4.96726e-05 | 0.00498335 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876929 | ACTGACGGTGCTGCC[C/T]GTGTCGTCCTCATCC | 11252 |
| rs374366725 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962310 | AAACATTTACACAGC[A/T]CTTACTTTATTTCTG | 11252 |
| rs374388575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960132 | CCTCCCCAACACACA[A/C]AAAATCAAATTATAT | 11252 |
| rs374415626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917777 | CATTTCCCTCACTGA[C/T]TGGTACTCTTTTCTT | 11252 |
| rs374449145 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890417 | ATCCTCAGTTACCAA[-/A]TCTGTAAAATGTGTT | 11252 |
| rs374456673 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990996 | AACGCTGTTGTGAGG[A/T]CTCAACGGGTTCTAT | 11252 |
| rs374460272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986701 | ACCACTGAGAGGGGG[A/C]TTTTGTGCTATGACC | 11252 |
| rs374468171 | in-del | -/GAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993870 | AAGAAATCACAAGAA[-/GAA]TGTGGCCCAAAAGGT | 11252 |
| rs374475288 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947676 | AAGACCCCTGGGGGT[G/T]GGGGGGGGGACCTCT | 11252 |
| rs374486852 | snp | A/G | 9.94349e-05 | 0.00705036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882165 | GGCTGATGAGCTCAT[A/G]GGCACACCCTCCTCT | 11252 |
| rs374517110 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969719 | CGAGGCATGATGATC[A/G]CTCGAGTCCACGTGT | 11252 |
| rs374527330 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911107 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 11252 |
| rs374527517 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988554 | TCCACTGGCCAAAAG[C/T]ATAACTGCTCCTAAC | 11252 |
| rs374531805 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941732 | TGCTCATTTTTTAAA[C/G]TGGTGTGTCTTCTTA | 11252 |
| rs374538877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942978 | ACTCTGTAGCTCAAT[C/T]TGAGGAGTACTGCCA | 11252 |
| rs374543971 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982506 | GAAGTAGACATGGGA[C/G]ACTTTTCATTTTGTT | 11252 |
| rs374593651 | snp | C/G | | | utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015131 | GCCCAGCCCTGCCCA[C/G]ACCCCTGCGGCCGCT | 11252 |
| rs374650540 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948840 | ACAAACTGATAAATG[A/T]ATTCTAACTTGACAG | 11252 |
| rs374683490 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956459 | TGTGACTATAGTGCC[-/C]TTCAAAAGTAATCAC | 11252 |
| rs374693507 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904328 | GGAGCCCTGGGTCTC[G/T]GGGAAGACATGCACT | 11252 |
| rs374696838 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983039 | TACAAAAATTAGGCC[A/G]GGCACAGTGGCTTAC | 11252 |
| rs374699895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942021 | ACCTCAGGTGATCTG[C/T]CCGCCTCTGCCTCCC | 11252 |
| rs374700873 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000405 | GACTGAGTTTGTCTC[C/T]ACCTCCACCAATCAC | 11252 |
| rs374701361 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016261 | GCTGCTACATATAGA[C/T]AGGTATGAGAAAAGA | 11252 |
| rs374732014 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920734 | ACGCCAAGCTCAGGG[C/T]TGAGAAATGCAAAGT | 11252 |
| rs374751323 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948169 | CCAGTGCAGGGTCCC[A/G]CTGGTCCTGGAGGGC | 11252 |
| rs374762889 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003095 | GCAGGACAGAGACAA[A/C/G]GTACCTCTCTTGCCT | 11252 |
| rs374773686 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949711 | TCACACACACTCTCT[-/CA]CACACACACACACAG | 11252 |
| rs374808412 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923002 | CAGGGGAGGGGTCTT[C/T]CCGGCAGAGGCAGAG | 11252 |
| rs374809612 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895269 | TGCTTCCCTTAAAAT[A/G]AGGCCTTACTGTCAT | 11252 |
| rs374831457 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933963 | CTGTTTAAAAATAAA[C/T]CGGATACTCAAATAC | 11252 |
| rs374832703 | snp | C/T | 0.0004746 | 0.0153972 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876373 | GCCCTCAGCACAGGG[C/T]GGCAGAGGGTGTGAG | 11252 |
| rs374842991 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014582 | GTCTCGGATTCCCAG[C/T]TTTCTCCTAAATCGC | 11252 |
| rs374845464 | in-del | -/GGAGAGAGGGAGAGAGGGGACCTGGAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950419 | GAGGGAGGGAGGGAA[-/GGAGAGAGGGAGAGAGGGGACCTGGAG]GGGAGTGGGCAGGTG | 11252 |
| rs374852510 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907931 | TGCAGTGCTAGAGTC[C/T]GAGAGAAACCAGCCC | 11252 |
| rs374888871 | snp | A/G | 9.96429e-05 | 0.00705773 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879140 | CTTCTCTCTCCGGCT[A/G]AGGGTTCGATTCAGG | 11252 |
| rs374905188 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912776 | CCACACCTTGCTAGT[A/G]TGATGACCTGTCCGC | 11252 |
| rs374914242 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880748 | GACCCACAGAGAGAA[A/G]GACCCCCTAGGCTCT | 11252 |
| rs374954364 | snp | A/G | 4.9689e-05 | 0.00498418 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891022 | GGTCTCCTTGAAGCC[A/G]CCCATCATCTGCTTG | 11252 |
| rs374958275 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921883 | AGCTGGGATTACAGG[C/T]GCTCACCACCATGCC | 11252 |
| rs374967283 | in-del | -/CCCCAGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957106 | CACTTCTTCTCTAGG[-/CCCCAGG]ATAATGTCGCCTGGC | 11252 |
| rs374983965 | in-del | -/ATTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875372 | TTGCCCAGGTTATTT[-/ATTT]GTTTGTTTGTTTGCG | 11252 |
| rs375019465 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893186 | GAGTTCTGAGTTAAC[A/T]CGGCAAGTGCAAGTG | 11252 |
| rs375032678 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968418 | TCCCTTCTCCTTCTA[C/T]ATTTTGGATCAGTGC | 11252 |
| rs375047094 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942572 | TCTGATCCATCTGGA[A/G]TTAAGTTTTATATGT | 11252 |
| rs375070362 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876636 | CATGGTGCTGCTAGG[G/T]CCTTGAAGGGTTAAC | 11252 |
| rs375157120 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942123 | TTTTTTTTTTTAATT[C/T]TTTCAATTTTTTTGG | 11252 |
| rs375164092 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918416 | CCATCCAAGCAGCTA[-/A]CCAGCTACTCAGTAC | 11252 |
| rs375224692 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966285 | TGAGGCAGGAGAATT[G/T]CTTGAACCTGGGAGG | 11252 |
| rs375231897 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987419 | CCACCCAGCATGTGG[C/T]TTGAGACACCCCACC | 11252 |
| rs375281563 | snp | A/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895575 | TAACAAGTCACATGT[A/T]GGTACCACCCATCGG | 11252 |
| rs375284466 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995749 | CATGTTTTCCTCCTT[C/G]AGAAAGGCAATTTGA | 11252 |
| rs375286837 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987110 | TTTTGATGACTTGCT[A/G]GGGGGTGTGTCTGAA | 11252 |
| rs375293300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923466 | AGAGTTTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 11252 |
| rs375311471 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939477 | AATGATTGGAAGTGA[C/T]GCAGTTAGAGCAGGC | 11252 |
| rs375315693 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912272 | CAGTACAGGGCGGTC[C/T]ATAATATTTCCTTTA | 11252 |
| rs375339247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922304 | AATGATGTATTCACA[A/G]GGACATCCAGCTCCC | 11252 |
| rs375344295 | snp | A/G | 1.65663e-05 | 0.002878 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876264 | GGCATCCGTGGAGGA[A/G]AAGGGGTTGTTAGAC | 11252 |
| rs375391086 | snp | A/G | 0.000165986 | 0.00910854 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912066 | TCCAACGGAATCATC[A/G]TATGTGACAGACATT | 11252 |
| rs375398257 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991571 | ATCCAGCGGGCATCG[A/C]CCAGTCCCTTTCCCA | 11252 |
| rs375483821 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872381 | TGCTGGCTCGGACCT[C/G/T]GTCAGGAGCAAGCAA | 11252 |
| rs375485210 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015654 | CGGGGGGTTGGGGGG[A/G]CGTATGTTGCTGCTC | 11252 |
| rs375585856 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932917 | TTTATTTTGCTTTTG[A/G]TCTTCAAAAAGGGGT | 11252 |
| rs375617635 | snp | A/G | 0.000157987 | 0.00888643 | missense | PACSIN2 | GRCh38.p7 | 22:42879144 | TCTCTCCGGCTGAGG[A/G]TTCGATTCAGGTCTG | 11252 |
| rs375629150 | snp | A/C/T | 3.32336e-05 | 0.00407624 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888604 | CGTCAACAACTGACA[A/C/T]GGTGACACTCGACGT | 11252 |
| rs375655899 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974351 | ATTAGATATGATCTA[C/T]TTCTAAACAGTAGGG | 11252 |
| rs375688127 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891653 | TCAGGTGATCCATTC[A/G]CCTCGGCCTCCCAAA | 11252 |
| rs375694890 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905969 | CACTCCTTCAAGTAT[G/T]TAAGTCCCTCCCATG | 11252 |
| rs375718691 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963833 | GTCATTTGGAAACAA[C/T]AAAATTTCTACAATT | 11252 |
| rs375791278 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985454 | CACTCCAAGGCTCCG[C/T]TGTGGCCCCCCACTG | 11252 |
| rs375809364 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992281 | ATGTACCAAGTGTTG[G/T]TGAGGATGTGGGGGA | 11252 |
| rs375832458 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899813 | TGTGCGCGACTACGC[C/T]GACACACTGACCCAG | 11252 |
| rs375840361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011171 | GTATGTGAGGGATCA[C/G]TGCCCTGGCCATAAG | 11252 |
| rs375855795 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920568 | CTCCCAAAGGCCTGC[C/T]GAATTAAGAGGTGGA | 11252 |
| rs375874057 | snp | A/G | 1.67435e-05 | 0.00289335 | missense | PACSIN2 | GRCh38.p7 | 22:42879055 | CCACTCACCTGCTGG[A/G]CTTACTCGGCAGAGA | 11252 |
| rs375877454 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953909 | AAGCCAGGGAAGAGA[A/G]GAATGCTTAGAGCAA | 11252 |
| rs375889142 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974547 | ATTAAAAGATCATAA[A/G]CACCAGCCATGGCCA | 11252 |
| rs375890928 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955828 | AATCAATAGATACTG[C/G]TGATCAGTCTACTAC | 11252 |
| rs375900593 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894251 | AGCTGAAGGCAATTG[G/T]TTTTTTTTTTGAGAC | 11252 |
| rs375914992 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886463 | GTAGGTATGTATGTA[C/T]CTACCTACTTACCTA | 11252 |
| rs375918995 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890879 | AGTCCTAGGTGCAGG[A/C]GGTGGTGCTGCTAGT | 11252 |
| rs375937242 | snp | A/C | 0.000159987 | 0.00894248 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882141 | TCTGTGGGCCCAGGT[A/C]CTCTTCCAGGCTGAT | 11252 |
| rs375970934 | in-del | -/CTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934903 | TCTTTCTTTTCTTTT[-/CTTT]CTTTCTTCCTTTTTC | 11252 |
| rs375975538 | snp | A/T | 0.000248532 | 0.0111447 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912003 | ACTTCATTCACTGGA[A/T]GAAAGCAGGTGCATT | 11252 |
| rs375976224 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886981 | CTCTCACACAGGCAC[A/G]CCCCCGCCCAACATG | 11252 |
| rs375978989 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016386 | AGGCACGGTGGCTCA[C/T]GCCTGGAATCCCAGT | 11252 |
| rs375987232 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963624 | ACTATAAGATAGGTA[A/C]TCCTAGCCCTGTTTT | 11252 |
| rs375998652 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939951 | TTAGTGGCAATCGGC[A/G]TCTACCCGGCCTTCA | 11252 |
| rs376022800 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923655 | GATGGTCTCGATCTC[C/T]TGACCTCGTGATCCG | 11252 |
| rs376049393 | snp | C/G | | | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873443 | ATAACCAGCCCAGGG[C/G]AAGAGTGTCTGGGGA | 11252 |
| rs376100015 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989183 | TGCACCTGGTCTAGT[A/T]CGTTTCTTAATACAA | 11252 |
| rs376119336 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946294 | TGCCACAGTCTAAGG[C/G]GGAAGTAAGGACAAA | 11252 |
| rs376148720 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983895 | AGATGTCATGTCAGG[G/T]CAGGAAATAAACTAG | 11252 |
| rs376153764 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903051 | TTCTGCCGCATTCCT[G/T]AGAGAGTCACATAAG | 11252 |
| rs376184850 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932276 | GACAAGCGTATGGCC[A/G]GCTCCCCCTCACACC | 11252 |
| rs376188023 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971286 | GAGACGGGGTTTCGC[C/T]GTGTTGGCCGGGCTG | 11252 |
| rs376200033 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878300 | GCAGCGGAATGACGA[C/T]AGCCACACCTGCTGG | 11252 |
| rs376264946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946411 | GGCCTCTGAGCCTGG[C/T]GAGAGCAGCAATGTA | 11252 |
| rs376289634 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938613 | CTGCACAGGCCAACT[C/G]CATGTTCCGCAGGAC | 11252 |
| rs376320718 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878031 | TAGGCCTGCTGGAGG[C/T]CAATATCCAGGCCAC | 11252 |
| rs376328330 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894729 | AAACGAAAATGTTCG[A/G]TATGTTTCATTCTTT | 11252 |
| rs376342669 | in-del | -/CCCCC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878299 | GCAGCGGAATGACGA[-/CCCCC]CAGCCACACCTGCTG | 11252 |
| rs376359013 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003325 | ATAAAAACAAATATC[A/G]GCTGGGCGCGGTGGC | 11252 |
| rs376373367 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990441 | TCCGCCTACCCAGCT[C/G]CTAGCCCCACAGAAG | 11252 |
| rs376375328 | in-del | -/AC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951863 | CCTTCCAATCCCCAC[-/AC]CCTGGACTCTGGCTA | 11252 |
| rs376383049 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906771 | AACTCTCCCCAAAAT[A/G]AGCATAAGAACCTTA | 11252 |
| rs376500667 | snp | C/T | 6.62581e-05 | 0.0057554 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876237 | GTCGTCGAATGGATT[C/T]GAGTCCCCATTGGCA | 11252 |
| rs376532015 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897936 | AATGGAACACAGAAC[A/T]CAGGGAGCAAATGGC | 11252 |
| rs376571968 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014336 | TACACACACACACAC[A/T]CACACACACACACAC | 11252 |
| rs376594688 | in-del | -/GATGAAAAATAACTGGTTTGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954894 | AACAAACTGGTTTGG[-/GATGAAAAATAACTGGTTTGG]ATCTGATAAATATGA | 11252 |
| rs376638524 | snp | A/G | 0.000415541 | 0.0144083 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871486 | TGCAAGACAAAGAGG[A/G]AGCCGTCTCCATGAG | 11252 |
| rs376673161 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910129 | AGCAGTCAAACCCAG[-/A]ACCTCCTGGCTCCAA | 11252 |
| rs376749606 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953633 | TGCAGTGCTAAGGGT[G/T]TCATTTAACACGAGG | 11252 |
| rs376763673 | snp | C/T | 0.000153988 | 0.00877328 | missense | PACSIN2 | GRCh38.p7 | 22:42884452 | CGGAAGAAGCGAAGG[C/T]GTTTCTCCTCGAACT | 11252 |
| rs376814426 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937982 | GCCTGGTTGATTTTT[C/T]CCAGCTAACTTGCTC | 11252 |
| rs376819100 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974658 | GGTGGCTGAGGCACC[A/G]TAACTGCTTAAACCT | 11252 |
| rs376839450 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951472 | CCTGAGCTCCAGATC[C/T]GGCATGGCCCGAGCT | 11252 |
| rs376851822 | snp | A/G | 3.3264e-05 | 0.0040781 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893581 | GCGGTGGCCATCGTC[A/G]ATCCGCTTCACAGTC | 11252 |
| rs376883396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931274 | GGGTAACCAGGGGCA[C/T]GTTACTTAACCTTCC | 11252 |
| rs376897966 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969783 | ATCTCTACGAAAAAT[G/T]TTTAAGCTGGGCTTG | 11252 |
| rs376903593 | snp | A/G | 0.000396412 | 0.014073 | missense | PACSIN2 | GRCh38.p7 | 22:42884438 | CCAGCAGAACCTCCC[A/G]GAAGAAGCGAAGGCG | 11252 |
| rs376932740 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910460 | GCCTCTCTGGGGGGG[-/G]CCAGCCAGCGGGACC | 11252 |
| rs376937167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966167 | ACGAGGTCAAGAGAT[C/T]GAGACCATCTTGGCC | 11252 |
| rs376967507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941997 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCAG | 11252 |
| rs376979947 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910135 | TCAAACCCAGACCTC[C/G]TGGCTCCAAAGCAAT | 11252 |
| rs376983137 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924104 | ATGAATGGCCCCATA[C/T]TAGAAGGAAGGGAGG | 11252 |
| rs376984480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884274 | TGAGGGCGGTGAGGA[A/G]ACCTCCTGATGAACG | 11252 |
| rs377009678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998485 | CAACAATAAACTTTT[C/T]CTGAACTTAAGCCTT | 11252 |
| rs377024421 | snp | C/G | 1.66059e-05 | 0.00288144 | missense | PACSIN2 | GRCh38.p7 | 22:42879128 | AGTGGCCTTCTTCTT[C/G]TCTCTCCGGCTGAGG | 11252 |
| rs377033443 | in-del | -/TTAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927577 | TATTTATTTATTTAG[-/TTAT]TTAGTTATTTAGTTA | 11252 |
| rs377037610 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987892 | ATGTCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 11252 |
| rs377059477 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921337 | GTCGCCCACCCTGGG[A/C]GACAGTGTGAGACTC | 11252 |
| rs377064634 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886303 | CTTAGGTGGATTGTA[A/G]TATTTTAGCACTAAA | 11252 |
| rs377069717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930634 | AAATAACAAAAGGCA[C/T]GCTCATAAAAAGCAA | 11252 |
| rs377075858 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949910 | CTCCCAATATTCTAA[A/T]AACATTTACTTTCTG | 11252 |
| rs377097257 | snp | A/G | 0.000328444 | 0.0128107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884342 | TCAAAAGCACTTTCC[A/G]TTGACTTCAATGACG | 11252 |
| rs377107463 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904289 | TGCACAGCATATGCC[A/G]CCCTGTGTGCCATCT | 11252 |
| rs377120168 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921004 | TTTCGTCGTATTGCC[C/G]AAGCTGGTCTTGAAC | 11252 |
| rs377121259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892155 | GAAGGAAGCCCTAAT[A/C]CAGGCTGGCATTTCT | 11252 |
| rs377165460 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914394 | TGTGCCACCACGCTC[A/G]GCTAATTTTTGTATT | 11252 |
| rs377189233 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949712 | CACACACACTCTCTC[A/T]CACACACACACACAG | 11252 |
| rs377217576 | in-del | -/AAGAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919825 | AAAAAGAAAAAGAAA[-/AAGAAA]CTGAGCTCAGCCAGG | 11252 |
| rs377248040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007347 | CAGCCTCCCGAGTAC[C/G]TGGGTTCACAGTCAC | 11252 |
| rs377262179 | snp | C/T | 1.65723e-05 | 0.00287852 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911996 | CCTGGCCACTTCATT[C/T]ACTGGAAGAAAGCAG | 11252 |
| rs377299322 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009804 | AATCTCTAGCCTTAT[A/T]TATCATTTTTAAGGC | 11252 |
| rs377302083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960728 | GAGGCAGGCAGGAAG[C/G]GGTGCCAGGAGGGTT | 11252 |
| rs377305975 | snp | C/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903748 | TTAGAGATTCAGAAT[C/G/T]GCCTTGAGTCTGATC | 11252 |
| rs377311424 | snp | C/G | 0.00119752 | 0.0244452 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972064 | CGGTTTTGTCCAATG[C/G]GGGGGGGAAATGTGG | 11252 |
| rs377321923 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882139 | ACTCTGTGGGCCCAG[C/G]TCCTCTTCCAGGCTG | 11252 |
| rs377325676 | in-del | -/CA/TC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949710 | TCACACACACTCTCT[-/CA/TC]CACACACACACACAC | 11252 |
| rs377331535 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870643 | AATTTTTAAATATGG[C/T]GATTTGGGGGAGTTC | 11252 |
| rs377341333 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950701 | GCTTTATCTAAAAAT[A/G]TATGTTTAAGAGTGG | 11252 |
| rs377420717 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002724 | AACTAATTACACAGA[C/T]GAAAAAGGATGAAAT | 11252 |
| rs377428263 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014414 | AGGAAGGAAATGGAG[G/T]CCGCTCATCAAAGCG | 11252 |
| rs377449552 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918797 | ATCTCTACCACATCC[C/T]CAAAGGCGCTGGGCC | 11252 |
| rs377451387 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950379 | TACTAGGAAAGATAA[C/G]ACAAAGTCATACCAG | 11252 |
| rs377512276 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907131 | CAGATCTTTGTGGAT[A/G]GGAGCCTGGGGTGGC | 11252 |
| rs377546902 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881339 | CATTCCCATTCCACA[C/T]GTGGGAAAACTGAGT | 11252 |
| rs377558178 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936748 | AAACCCCATCTCCAC[C/T]AAAAATACAAAAATT | 11252 |
| rs377591263 | snp | A/G | 0.000313203 | 0.0125101 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884463 | AAGGCGTTTCTCCTC[A/G]AACTGCTGGCACTGC | 11252 |
| rs377688332 | in-del | -/AG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890699 | CAGCCTGGGAGAGAG[-/AG]TGAGACTTTGTCTCA | 11252 |
| rs377705808 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941837 | GCTGGAGTGCAGTGG[C/T]GCATTCTCGGCTCAC | 11252 |
| rs377715805 | snp | C/T | 0.000630005 | 0.0177371 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876855 | GAGACAGAGTGAGCG[C/T]GGTGGGAGCAGAGGA | 11252 |
| rs377729506 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900868 | CCACCTGCCCAAACA[A/T]CCCTCAGGCCGGGAT | 11252 |
| rs377735877 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913733 | ATTTTAAAGTCAAGA[C/T]AATTGATGTTCAGTA | 11252 |
| rs386395522 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898284 | TCCTTTTCTTTTTTT[-/T]TTTTTTGAGACAGTT | 11252 |
| rs386395523 | in-del | -/TCTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934907 | TCTTTTCTTTTCTTT[-/TCTT]CTTCCTTTTTCTTTT | 11252 |
| rs386395524 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962195 | AACTTTTTTTTTTTT[-/TT]TGTCCCAGAGCCCCA | 11252 |
| rs386821577 | multinucleotide-polymorphism | AC/CT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904614 | TCCAAAGCCGATGAT[AC/CT]AGTGGGGAAACGCCA | 11252 |
| rs386821578 | in-del | CC/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904723 | GCTTCCACAGCCCCC[CC/G]ATACTGCACTCCAGT | 11252 |
| rs386821579 | multinucleotide-polymorphism | CCG/GCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931573 | TCCACAAAGCCGATG[CCG/GCT]GCCCTGAAACAGGAA | 11252 |
| rs386821580 | multinucleotide-polymorphism | ATA/GTG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943870 | TTTGCACAATACAAT[ATA/GTG]GAAAGCAAAGAAAGA | 11252 |
| rs386821581 | multinucleotide-polymorphism | GC/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944273 | AGACATTTGTGTTAG[GC/TT]TAAGTCTCTGAGACT | 11252 |
| rs386821582 | in-del | AA/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967115 | GTGCTCCGTAACAGA[AA/C]CTAGGCAGGGAATGT | 11252 |
| rs386821583 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967882 | CGCAGAGCGAGACTC[CA/TG]TCTCAAAAATAAAAA | 11252 |
| rs386821584 | in-del | A/GAGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974785 | AGAAAAGAGAAGAAG[A/GAGG]AGGAGGAGGAGGAGA | 11252 |
| rs386821585 | multinucleotide-polymorphism | AG/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979694 | ATATGCTCTGTCTTA[AG/TA]GCACCTGCCGCTTTC | 11252 |
| rs386821586 | in-del | CT/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990830 | GCCATGGAAACCACT[CT/G]ATTTGGCTCAAGAGC | 11252 |
| rs386821587 | multinucleotide-polymorphism | ACCACAGG/GCCACAGT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010667 | GTGAGCCAAGATCAC[ACCACAGG/GCCACAGT]GCACTTCCAGCCTGG | 11252 |
| rs386821588 | multinucleotide-polymorphism | GG/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010674 | AAGATCACACCACAG[GG/TA]CACTTCCAGCCTGGG | 11252 |
| rs386821589 | multinucleotide-polymorphism | ACA/CCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014322 | TGCTCCCCCCGCCCT[ACA/CCT]CACACACACACACAC | 11252 |
| rs386821590 | in-del | ACACACACACACACACAC/CCTCAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014322 | TGCTCCCCCCGCCCT[ACACACACACACACACAC/CCTCAG]ACACACACACACAGA | 11252 |
| rs386821591 | in-del | CACACACACACAGACACACACACACCACCCCCCCCCCCCC/GAGCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014341 | ACACACACACACACA[lengthTooLong]GGGACACGGAGGGTG | 11252 |
| rs386821592 | multinucleotide-polymorphism | AAC/GAA | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015879 | AGAGGATGGTGAGAG[AAC/GAA]CCCCAGGTGAGGGGT | 11252 |
| rs397706717 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009014 | TTTCACATACAGAAA[-/A]GGTGTTTAGTGATCC | 11252 |
| rs397737140 | in-del | -/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957421 | GAACCTCCCCAAGGT[-/T]ATTTTAAGGTGACTT | 11252 |
| rs397742505 | in-del | -/A/C | 5.02269e-05 | 0.00501108 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871336 | CGCCTCCGTCCCCCC[-/A/C]GCTGGCCTGTCCCCG | 11252 |
| rs397744211 | in-del | -/G | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880826 | GTGCCCCTCTTTGGG[-/G]TATAATGGGCACCTC | 11252 |
| rs397753419 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963855 | CTACAATTTTTTTTT[-/T]CACCACTTCTCTACT | 11252 |
| rs397762950 | in-del | -/C | 0.375 | 0.216506 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875800 | CCTGTAATCCCAGCA[-/C]CTTTGGGAGGCCAAG | 11252 |
| rs397768572 | in-del | -/T | 0 | 0 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873811 | CCTTTTTTTTTTTTT[-/T]GAGACAGAGTGTCAC | 11252 |
| rs397785065 | in-del | -/AG | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871938 | CTTCCAGGCTGCGAG[-/AG]GGGAAGGGACCATGT | 11252 |
| rs397802089 | in-del | -/T | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973433 | TACCACACTGTTTTT[-/T]GTCAACAAGGCTCCA | 11252 |
| rs397813814 | in-del | -/AG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876834 | TGGACAGAGAGAGAG[-/AG]GAAGAGAGACAGAGT | 11252 |
| rs397823905 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908040 | TCTTCAGGGCTAACA[-/CA]TTCCCAGAATATTTG | 11252 |
| rs397940058 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875553 | TAATTTTTTTTTTTT[-/T]GACACAAAGTCTTGC | 11252 |
| rs397940071 | in-del | -/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975621 | TATTCTTTTTTTTTT[-/TT]CCCTTTTTCTAACCA | 11252 |
| rs398037261 | in-del | -/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936232 | TGGAATTCTGTAGGA[-/T]TTTTTTTTTTTTTTT | 11252 |
| rs398037262 | in-del | -/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945229 | CTCGTCCCCCACTGA[-/T]TTTGCTTCTGTCAGC | 11252 |
| rs398040510 | in-del | -/A | 0.5 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969932 | AAAAAGAAAAAAAAA[-/A]GAAAAGAAACTAGAA | 11252 |
| rs398081799 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926684 | CAGGAAAAAAAAAAA[-/A]ATCATTCTGGAGCTG | 11252 |
| rs398081800 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934902 | TCTCTTTCTTTTCTT[-/T]TCTTTCTTCCTTTTT | 11252 |
| rs398121850 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921754 | CTTTTTTTTTTTTTT[-/T]AGACAGAATCTTGCT | 11252 |
| rs527246382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884164 | GCCGGGTCAACCAGG[C/T]CTTCCAGAGGTCCAG | 11252 |
| rs527251447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971029 | GTTTCTGAGGGTCTG[C/T]AGGCTAACGCTAAGC | 11252 |
| rs527264974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010437 | AAGACCGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 11252 |
| rs527265169 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016341 | ATTGTCCTTATGACA[A/G]TAATTGAGAAAGAAA | 11252 |
| rs527277769 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009839 | TGCGAGGTCTTTGAT[A/G]GTTGAGACATCATTT | 11252 |
| rs527290996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884786 | AGCAAGGCCCAGACA[A/G]GTAGATGCCGGCAAA | 11252 |
| rs527308132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964734 | ACGACAAAGTTAGAC[A/G]AAAGACCAAAAGGAG | 11252 |
| rs527314980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928148 | TCAATCTACACTTAA[A/G]GGGCAAACCATAAAC | 11252 |
| rs527315938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921485 | GTGGCCACTCTCCCA[C/T]TTAGGGGAAGGGCCA | 11252 |
| rs527335877 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004607 | TTCATGATCTTGGCA[C/G/T]GCTCGGTTGGCGACA | 11252 |
| rs527342382 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988767 | CCACACATTCCAAAG[A/C]AACATTTTCAAAAAC | 11252 |
| rs527376049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921895 | AGGCGCTCACCACCA[C/T]GCCAGGCTAATTTTT | 11252 |
| rs527400355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997857 | CTGCACCCCAGCCTG[A/G]GCGACAGGGCAAGAC | 11252 |
| rs527412390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005197 | ACACCTTTATCATTT[C/G]CTTTCTAAGTCCTAT | 11252 |
| rs527417593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959122 | ATGAGAAGAACTGAG[C/G]GGGAGGATGGGAAGG | 11252 |
| rs527433543 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986006 | AGGTCTTCTTGATTG[A/G]GCCAATGCCCCAGGT | 11252 |
| rs527437011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879338 | CTCAGGCTCCCCATG[C/T]CCCACTTATGAACCC | 11252 |
| rs527445884 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909262 | ACAGCCAAAGGCTCC[C/T]GGAGGACAGGGCCAC | 11252 |
| rs527464646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874012 | CCAGGCTGGTCTCAA[A/C]CTCCTGACCTCAAGT | 11252 |
| rs527470631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952516 | GGCGCGCACCACCAC[A/G]CCTGGCTAATTTGTT | 11252 |
| rs527481129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959539 | TCATTTGTTTAAGCC[A/G]AAATCTATTCTCCAA | 11252 |
| rs527484734 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946527 | TGCACTCCAGCCTGG[A/G]GGAAAGAGCAAAACT | 11252 |
| rs527496148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952764 | GCCTCCCAGGTTCAA[A/G]CAATTCTCCTGCCTC | 11252 |
| rs527511704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991905 | GTAAAACATAAAACT[A/G]TAACATTTCTAGACG | 11252 |
| rs527545920 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919076 | CTGCTCTTTAATGCC[-/A]AACAGTGCTGGAGCC | 11252 |
| rs527548687 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004683 | AATGCTCACAAACTA[C/G]GGTTTGGGTATCACT | 11252 |
| rs527556021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42946949 | GCTCCATTCCCCTTC[A/G]TGCCAGTCTTCAGGA | 11252 |
| rs527567613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909864 | GGGTAATGAAGACAA[C/T]GTCGCCAAGGGCACC | 11252 |
| rs527575397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992487 | GTGCAGTGGTTCACA[C/G]CTGTAATCCCAACAC | 11252 |
| rs527582834 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903456 | AAGAGTAACAGGGGT[A/C]CTTGAAAAACCATCT | 11252 |
| rs527627142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903954 | AAAGCACCCCTTGCC[A/G]TTTGATCATTTAAAA | 11252 |
| rs527652135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986548 | CGGAGGCCTTTTGGG[G/T]CCCTGCACGCTGCTG | 11252 |
| rs527656281 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940559 | AGTGCCACCAGAATA[G/T]GAGCCCCGCCCTGGG | 11252 |
| rs527660268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898686 | ATCCACTCCCTTCCC[C/G]ATGCCCTTCCCCGAG | 11252 |
| rs527674547 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949363 | GGAGGATATGGCTTT[-/G]GCAAGCAGGACTTAC | 11252 |
| rs527697027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892393 | AACAGAGAACAGCCC[C/T]GGAAGTTGGACCTCT | 11252 |
| rs527709299 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955424 | CAGAGCTCACTCAGG[C/T]GCCTGCATGTCTACC | 11252 |
| rs527709387 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980073 | AACAAGTTGTTAATT[-/A]AAAAAAAAAGAAAGA | 11252 |
| rs527718222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934955 | GAGTTTCGCTTTATC[A/G]CCCAGGCTGGAGTGC | 11252 |
| rs527741765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929131 | TCCAGGCCTGACGGC[C/T]GCCCTGTGCAACTAT | 11252 |
| rs527763109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971688 | AGTGAGGAGCCCCTC[C/T]GCCGGGCAGCCGCCC | 11252 |
| rs527780678 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933817 | CATTCTTGGAAGTTA[C/T]GAATAAGATATTCTG | 11252 |
| rs527813553 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893004 | GAAACCTCTGCCATA[C/T]AACACCTGTAATTAT | 11252 |
| rs527819021 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931777 | ACGTTGTTATTATTA[C/T]GGTTAACAACCAGGG | 11252 |
| rs527832402 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007607 | GCTCTGGCACAATCC[C/T]TCCCAAGTCACTTCC | 11252 |
| rs527833277 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885500 | CTAACAACATGTGCA[C/G]GGCCTTCTGAGGAAG | 11252 |
| rs527847127 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886250 | ATAGAAAGTTCTCAG[A/C]GAACACCCATGGAGT | 11252 |
| rs527873276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002896 | AAAATACTTGAGAAA[A/G]TATTTAAGTGAATCT | 11252 |
| rs527896420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012279 | CTGAGGCAGAGGAAT[A/C]ATTTGAACCTGGGCA | 11252 |
| rs527905543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923332 | CTGGTCTTAAGTCCC[C/T]TGTGCAGAGTAAAAG | 11252 |
| rs527921063 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992412 | ACCTAAACCACCAAA[A/G]CACCTAGCCATTCCA | 11252 |
| rs527929034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006035 | TGGCATCAAGTGATC[C/T]TCCTGCCTCAGCCTC | 11252 |
| rs527940990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999153 | AGGAGGGCTAAAAGA[A/G]CATTGTAACAACCCT | 11252 |
| rs527944056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006764 | AGGGTGCAGTGAGCC[A/G]AAATCGCACCATTGT | 11252 |
| rs527948499 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977491 | AAACAGAATGGTGAA[A/G]AACAGTTTTTAGTTA | 11252 |
| rs527985546 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927877 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCTCAGTC | 11252 |
| rs527993000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917716 | GGCACAGTCTGTCGA[G/T]CTTGGCCTTTCAGAA | 11252 |
| rs527994600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910631 | GTGAGATGTGGCTGG[C/T]GACCTGTTTGGCTGT | 11252 |
| rs528013793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960747 | GCCAGGAGGGTTTTG[A/G]AGCTGTGCTGTGGCT | 11252 |
| rs528025365 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004671 | TTAAAACATGAAAAT[A/G]CTCACAAACTACGGT | 11252 |
| rs528028719 | in-del | -/TTGTTCTGT | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984973 | TATATGTGGATTTGC[-/TTGTTCTGT]TTGGCAACCAAAGGT | 11252 |
| rs528042752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901321 | CTCTAGCATCTCCTC[C/T]GTCAGCCTGGCAGAC | 11252 |
| rs528049308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982665 | TTGTTAAACAGATGC[C/T]TGAAGGCAGCATGCT | 11252 |
| rs528057707 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012038 | TAGTCCCAGTTACTC[A/G]GGAGGCTGAGGCAGG | 11252 |
| rs528111646 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902623 | CTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 11252 |
| rs528116452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944161 | CCTCGAGTGGCAGCT[C/T]TCAGAGAGTGCTGTC | 11252 |
| rs528116723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937170 | ATGCAGAGAAATAAG[C/T]GAGGATGAGATAGGG | 11252 |
| rs528126924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931829 | TCTCTTCCAAAACAG[C/T]CCAGAAAATGTCACA | 11252 |
| rs528158254 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016075 | CCAGGCATGGTGACA[C/T]GCACCTGGAATCCCA | 11252 |
| rs528171765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983261 | GGTGGAGGCTGCAGT[A/G]AGTCGACAATGTGCC | 11252 |
| rs528184906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901630 | GGGGTTTACACTGCA[C/T]GGTAGGTTTCTTCCC | 11252 |
| rs528187020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879987 | CTGGCTTCACCAACC[A/G]CACTGAAAATGGACT | 11252 |
| rs528196432 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977675 | GCAGGGGAGGGACCT[C/G]ATGGGAGGTGATTAG | 11252 |
| rs528204751 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932326 | GAATCTAGCCACACC[C/T]CCCACCACCACCAAC | 11252 |
| rs528220318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895335 | CAAGCAACTCAGTAT[C/T]GTTGAGCTGGTGGTA | 11252 |
| rs528226734 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904160 | TGTTTACGCAAAGCT[A/G]TGTTGAACTAACTCT | 11252 |
| rs528226825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878062 | ATGTCTGAGCTCACC[A/G]GCCCTCCTCCCTCCT | 11252 |
| rs528233398 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968864 | GGGTTCTTAGGCCTT[C/T]AGCACTGGACTGAGA | 11252 |
| rs528252981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889689 | CACATCTACCGTCTA[C/T]TCCATTCCAGCTAGG | 11252 |
| rs528293779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963112 | GCTTCTGTCATCAAA[C/G]ACTGGAAACCATTGG | 11252 |
| rs528294326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882764 | CACCCACCACCAAGA[C/T]GGGGTGGGGGCTGCC | 11252 |
| rs528302782 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015135 | AGCCCTGCCCAGACC[C/T]CTGCGGCCGCTTCTG | 11252 |
| rs528331818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002174 | CCCATGAGAGCAGCA[C/T]CTAGAAGCTAGAGAT | 11252 |
| rs528343073 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926696 | AAAAATCATTCTGGA[C/G]CTGAGTGCACCTGTG | 11252 |
| rs528404314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963558 | TTGTTATATGATTGT[C/T]GCATGGTAAAAATGA | 11252 |
| rs528405184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002899 | ATACTTGAGAAAATA[A/T]TTAAGTGAATCTGAA | 11252 |
| rs528411820 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962306 | CAATAAACATTTACA[C/T]AGCACTTACTTTATT | 11252 |
| rs528448221 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878094 | GGCACCTTTCTCTAG[C/G]AGACTGTTGTGAGAC | 11252 |
| rs528448722 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935064 | AGGACTACAGGTGCC[C/T]GCCACCGCGCCCGGC | 11252 |
| rs528450201 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968029 | TGATAACCTTGCAAG[A/G]TGGGAGTACTGCGCC | 11252 |
| rs528482935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957268 | TAAATTAAAATAGTT[A/G]TAAAGTTATTAAATT | 11252 |
| rs528484199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872212 | CTGGTCTCAAGGAGG[A/C]AGACTAGGGTGGTGA | 11252 |
| rs528543982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951675 | ACCTCTACCTCAAAA[C/T]AGAGCCAGAATGTGG | 11252 |
| rs528560965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990570 | GTGAAATTAGAGCCA[A/G]GTTTTGAAGGATGAG | 11252 |
| rs528563120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945066 | TCATACCACTGTACT[C/G]TAGCCTGGACGACAG | 11252 |
| rs528572995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997148 | GGGGGTGTTTAATCA[C/T]GCTCTGCCTCCTCTG | 11252 |
| rs528610936 | in-del | -/AT | 0.00915039 | 0.0670184 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875139 | CAGGCGTGAGCCACC[-/AT]ATGCCCAGCCTACTT | 11252 |
| rs528614171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896333 | CCATGTTGCTATCTA[C/T]GTCAGAAGGTCACTC | 11252 |
| rs528634337 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984870 | GAGGCAACTACTTAC[C/G]TGAAAAAAGCAGCTG | 11252 |
| rs528673893 | snp | C/G | | | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873667 | CCAGCTTCCCTCTTG[C/G]AGTGGTAGATGCTGC | 11252 |
| rs528675559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945542 | CCACTCCTGTTCCTG[A/G]GTTTTCTACGTCAGA | 11252 |
| rs528738419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933945 | AAACTCCAGTTCACA[G/T]AACTGTTTAAAAATA | 11252 |
| rs528788660 | snp | C/G | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897175 | TTCCTGGGCTCAAGC[C/G]ATCCTCCCACCTTGG | 11252 |
| rs528828238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970588 | ATTCTTGTAAAATAA[A/G]AAGTTTATTATAGAA | 11252 |
| rs528831334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976872 | CTAACGTCAGAGAAT[C/T]AGTAAATGGCAGGAC | 11252 |
| rs528835743 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880450 | CCAATGGGATCAACA[A/C/T]CAAGCCGGCACTGAT | 11252 |
| rs528893203 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880154 | AGTCCACGGCTCTGC[C/T]CACACGTACTTACAG | 11252 |
| rs528916916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917078 | TCATGTGCCAGACAC[C/T]GCGCCCCATGCACTA | 11252 |
| rs528950702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004914 | TTTCTCCTCTAAACA[A/T]TGAAAAGGGAAACAA | 11252 |
| rs528951017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954162 | CAGCTACTTGGGAGG[C/T]TGAGGCAAGAGAATC | 11252 |
| rs528962822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993673 | ACGTTGATGATAACA[C/T]GATTGCAGACTGTCA | 11252 |
| rs528970621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904565 | GACTGACAGGGAGTG[C/T]GAGAGACATCCAAAA | 11252 |
| rs528974140 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884862 | CACGCCCATGTCCTC[C/T]TCTCCCTGTGGGGAA | 11252 |
| rs528977650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910511 | CTGCAAGCGGGGGCA[A/G]AGGCAGTCCTGAATT | 11252 |
| rs528993404 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911003 | TCCGCCTCCCGGGTT[C/T]ATGCCATTCTCCTGC | 11252 |
| rs529006681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899353 | GCGCAGTGGTGCCAT[C/T]TCGGCTCACTTGCAA | 11252 |
| rs529006779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905090 | AAATTTTATCTTCAT[C/T]TACAGAAATGCACAA | 11252 |
| rs529059695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978630 | GGTAAGTTGTGGGAG[A/G]CAGTCGGGCAACATT | 11252 |
| rs529074410 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870019 | GTCACGTGAAACACA[C/G]GTTCCCCCACGTTCC | 11252 |
| rs529078915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941551 | TTCCCATATCCTCAC[C/T]AACACATGTTGTCTT | 11252 |
| rs529080946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948034 | TGCTACGGGGACACA[C/T]AGAGGGTCCAGAAAG | 11252 |
| rs529162828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979177 | CCATACCACTGCCCA[A/G]GGCCCAATGATGGTT | 11252 |
| rs529189176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930599 | AAATGCATTTGGAAG[A/T]ATGAAAGTAGGTCAT | 11252 |
| rs529199422 | snp | C/T | 1.70568e-05 | 0.0029203 | missense | PACSIN2 | GRCh38.p7 | 22:42893466 | CCATACCTTTCTCCA[C/T]GAGCTGCCTCCAGCG | 11252 |
| rs529232692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979904 | ATGCCAACTGTACTT[G/T]TCATTGTAAATTTAC | 11252 |
| rs529253773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972382 | GCGGAAGGCCGCAGG[G/T]TCCTCTGCCTAGGAA | 11252 |
| rs529255395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894093 | CTACCATGTGCCAGG[C/T]GACCTGCTAGGTGTT | 11252 |
| rs529262650 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967209 | CTCTGAGCTGAATCA[A/C/T]GTAAACAAGGGCCGT | 11252 |
| rs529272179 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999209 | AAAAGTGCTCGCCTC[A/G]GCCCCTGTACTTGCT | 11252 |
| rs529293962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887883 | ATGCCACAGTGCCTG[A/G]TCACGGTCTCTCCTT | 11252 |
| rs529295534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923865 | AAGATGGTGAGATCC[A/C]ATCTCTAAAATAAAT | 11252 |
| rs529306323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880887 | TTCCTGTGCCACTCC[A/G]GGAGCAGCAAATCCT | 11252 |
| rs529309393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924568 | CTGCTCACCTCCACC[A/G]AGCTACTTTGTCCTC | 11252 |
| rs529335860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931156 | CTCACACCTGCCTTG[A/T]TCACAGTTGTATCCC | 11252 |
| rs529370128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918449 | CTCAGCACCAACAGA[C/T]GGGTGAGGTGAACTT | 11252 |
| rs529389594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000835 | AAGGAGACATACTGT[A/G]TGGCACTGCCGTGAT | 11252 |
| rs529402172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961632 | ACAAAAATTGGCCAG[A/G]TGTAGTGGCACATGC | 11252 |
| rs529446465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881427 | TCTGAATGCAGCCCG[A/G]GCTCTGGCCGCTGCT | 11252 |
| rs529449909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948972 | GCTTAAATCAAGCAT[A/G]AAATTAATAGCAAAA | 11252 |
| rs529500635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911897 | TCTAGGTCTGACTAC[A/G]AATGCATGGCTGGTT | 11252 |
| rs529511324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949529 | CCAGTGACCACTTAT[A/T]AAGGGGAAAAATTAA | 11252 |
| rs529537834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905887 | CCAATTCTGCAGCTG[C/T]TGGAACACAGCAGGA | 11252 |
| rs529544981 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870894 | AATTTAAGTAGAAAT[A/G]AACAGGTGTATAAAA | 11252 |
| rs529545608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994211 | CGCTCCTGCTCAAGT[A/G]TGGCTGGTTTGGTGG | 11252 |
| rs529622662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989172 | GTATGAGCCACTGCA[C/T]CTGGTCTAGTTCGTT | 11252 |
| rs529625212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933299 | AGCAATGAGATGTAG[A/G]AAGGTACCTCTCTGA | 11252 |
| rs529625657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896827 | GCCATTCTACTTAGT[A/G]TAGCAATATTGCATT | 11252 |
| rs529644884 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015709 | GCAAGGCACCAGGCA[A/G]TGCACACGCATTCTT | 11252 |
| rs529660735 | snp | C/T | 0.000281443 | 0.0118593 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890917 | CAGGCAGAGCAAGGC[C/T]GGGCAGGGAAGCCTG | 11252 |
| rs529660877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009820 | TATCATTTTTAAGGC[C/T]TCTTGCGAGGTCTTT | 11252 |
| rs529675210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963802 | ATGAAAATCAAGATA[C/T]TTGGCAAAAGGTCGT | 11252 |
| rs529689768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926818 | ACTGCACTCCTGCCT[A/C]GGCAACATAGAGAGA | 11252 |
| rs529699642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933869 | GATGCTGAAGTGTGT[G/T]AAAGTATGAACAAGC | 11252 |
| rs529715492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883740 | GCCAGGTGCGGTGGC[C/T]CACGCCTGTAATCCC | 11252 |
| rs529736174 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872111 | GGTTCCATTTATCTT[C/T]GGTTGTTCCAACCTG | 11252 |
| rs529738799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969658 | GAAAGTAGAAACTAG[C/G]TCAGGCACAGTGGTT | 11252 |
| rs529786561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010197 | CTATATTCTCATCTC[C/T]GTCTAGTTCAGTGCC | 11252 |
| rs529787483 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922463 | GGCCTCGGGAGAAAG[C/T]CCCCGATACCCCGCT | 11252 |
| rs529792276 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923839 | GCCAGGAATTCAAGA[A/C]CAGCCTAGGCAAGAT | 11252 |
| rs529829192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964257 | ACCCTGTCTCCACTA[A/G]AAGTACAAAAATTAG | 11252 |
| rs529844625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951847 | CAGCGCCAGTCTCGC[C/T]CCTTCCAATCCCCAC | 11252 |
| rs529847011 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946547 | AGAGCAAAACTCTGT[C/T]TCAAAAAACAAAAAG | 11252 |
| rs529870816 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921886 | TGGGATTACAGGCGC[G/T]CACCACCATGCCAGG | 11252 |
| rs529881457 | snp | C/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017475 | GTGCTGGGATTACAC[C/G]CACGAGCCACTGTAC | 11252 |
| rs529892201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878931 | GCCACGGCCCACAGA[A/G]CTCAGGAGCCCAGGA | 11252 |
| rs529905513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945773 | CTAATCCTTAACAAC[A/G]TCCTAACTAACCTGC | 11252 |
| rs529907070 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873579 | GTTGGGGTGGTGGTG[G/T]TAAGGCAGCCTTTCC | 11252 |
| rs529914010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872903 | ACCATCTCTTTCCAC[C/T]GCTTCGTGCCTCGGG | 11252 |
| rs529934669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914828 | ATGCAGCTGTGGTCT[G/T]GACACAGTTCTGCAC | 11252 |
| rs529941031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991214 | GAGCCACTTTGTGAC[C/T]GAAGGGAAAAGAATG | 11252 |
| rs529950683 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924516 | GCTCTTAAGCCCCCC[-/A]ATGCAGAGTAAAAGC | 11252 |
| rs529955257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909217 | TGGCATGATGACCTG[C/T]CTAGTGTCTACCTTA | 11252 |
| rs529960456 | snp | A/C | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872055 | AGAAGGAGCCCCTGG[A/C]GCTGTTCTGGAATCT | 11252 |
| rs529972947 | in-del | -/CA | 0.00600956 | 0.0544855 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006357 | TTTGGCCAAAAGCCG[-/CA]CAGTCACCTAGTGAT | 11252 |
| rs529973801 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967931 | TGATCAAATTAGGTA[C/T]TTTACTGAGTGCATA | 11252 |
| rs530012840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908409 | AAGCACTGGTGACAC[A/G]TGAAAAGCCCCAAGG | 11252 |
| rs530014580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997820 | CGTGAGGTGGAGGAT[A/G]CAGTGAGCTGAGATC | 11252 |
| rs530043037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946861 | CAGGAGACATGTGGA[C/T]CATGTTGCAGGGAGC | 11252 |
| rs530049035 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993963 | ACCCCCAAGCCACAG[C/T]ATCTGTGGTTTGCTG | 11252 |
| rs530109687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940455 | GGTAGCTCTCAAACT[A/T]CCTCCTCAATCCACT | 11252 |
| rs530114129 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940103 | GGCTGTAGGCAGGAG[C/G]GGGACAATGCTTGCT | 11252 |
| rs530123684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986139 | ACAGTAAGCATTAGG[C/G]AAGGGAAAAACAAGA | 11252 |
| rs530126493 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892062 | GAGAGGAGGAAGCAG[A/G]AGCCTGCTCTGGACC | 11252 |
| rs530153587 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988822 | TAAAATTTACAATGA[C/T]ATCACATGCATTTGG | 11252 |
| rs530180268 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977678 | GGGGAGGGACCTGAT[A/G]GGAGGTGATTAGATC | 11252 |
| rs530189109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971600 | AGTCTGGGAAGTGAG[C/G]AGTGTCTCTGCCCAA | 11252 |
| rs530191988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977112 | CACATATTACATTCA[C/T]ATGAGACTGATCTGT | 11252 |
| rs530192485 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972185 | CTTCTGCCTTGGGAC[A/G]CTGTTGATCTATGGC | 11252 |
| rs530199809 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870236 | ACGGAGCCAGGACAA[A/G]GGCCGGTCAGAAGCC | 11252 |
| rs530202248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892295 | ACAGTGACCAAGTGC[A/G]CTGAGTCATGACAGA | 11252 |
| rs530203135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898046 | GCTCAGAAGGCTGGC[A/G]GGGGTGGGGACATCC | 11252 |
| rs530242623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891696 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCATGCCT | 11252 |
| rs530252718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971941 | AAGGTGGGGGGTGCC[G/T]CTGCCCGGCCGCCCC | 11252 |
| rs530303374 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928370 | GAAGGAGGAAAGAAA[A/G]GAAGGTGTTCACATA | 11252 |
| rs530309387 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928497 | TTTAAGAAACTTCAA[A/C]TACATAAGCCTCATT | 11252 |
| rs530320570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017456 | CCTGCCTCATCCTCC[C/T]AAAGTGCTGGGATTA | 11252 |
| rs530322225 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917059 | CCACCCCTATGGCGA[C/G]TCCTCATGTGCCAGA | 11252 |
| rs530348341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005946 | TGAATGGGACTAGTG[C/T]CCTTACAATTTTTTT | 11252 |
| rs530358987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966251 | GGTGTGCACCTGTAG[C/T]CCCAGCTACTTGGGA | 11252 |
| rs530359024 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938882 | GCTGTCTGTGACAAA[C/T]TTGTATTTTTTAAAA | 11252 |
| rs530366177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929050 | AACGTGAATTAAAGC[C/T]GAGTAATTATAAGAG | 11252 |
| rs530376721 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922654 | GTGGTTGGGAAATAA[C/T]GATTTATTCTAAGCC | 11252 |
| rs530378549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929505 | TTCAGTGGGAGTGGC[A/G]TGCCTACGAATGGCT | 11252 |
| rs530426970 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913761 | GTAATTTGCCCACGG[-/T]TGTCCAAGTAATGGC | 11252 |
| rs530447318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916612 | CTCTCACCCTGACAA[G/T]CCTCCCTTTCCTCCC | 11252 |
| rs530457763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959702 | TGAGAGTTCTGTTAA[A/C]TCAGTCACTCAGTGA | 11252 |
| rs530474451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905756 | CCAAAATAAACTGCC[C/T]GGCTGGCTCCCTGCA | 11252 |
| rs530505576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980013 | AACCTATGAAATAAG[C/T]GCATCATTGTTTCCA | 11252 |
| rs530514192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900571 | CGCAACCTTCCCGTC[C/T]GAAGTGATCCTCCTG | 11252 |
| rs530525824 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870454 | GACGAGTGCTTTAGA[C/T]TCTCTGAATATCAAA | 11252 |
| rs530549419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894280 | ACACAGTCTCGCTGT[C/T]GTCAGGCTGGAGTGC | 11252 |
| rs530565939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973473 | CCTCCTTTAACTTCT[C/T]ATTGAGAAAAAGACT | 11252 |
| rs530584738 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888150 | AGGCTCAGGCCTTCC[G/T]GAGTGGCTCCTGGTC | 11252 |
| rs530599147 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968307 | TTCATAGTCCCTAAT[A/G]ACCAACTCAAACCCT | 11252 |
| rs530600731 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996824 | CAAGCTGCATGCTGA[G/T]CAAAACCACACATCA | 11252 |
| rs530607666 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948929 | AAACAGGGAACTCAA[C/T]TGTCAGGCAACAATC | 11252 |
| rs530663525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901232 | AGAAGAGCTCCTGGC[A/G]TACCCCTCGCCAGGC | 11252 |
| rs530701665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894772 | TGAAAGGCTACAGTC[A/G]CTGATAACTTGAGCA | 11252 |
| rs530704804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008184 | AAATAAAAATAAAAA[A/C]CATCTTTATTATGAT | 11252 |
| rs530715808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915585 | CCATGTGCATTACTT[A/C]AGAGTTCATCTTAAT | 11252 |
| rs530735002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914116 | GAACTCCAGTGAGGG[A/G]TTCTCCCACACTGGT | 11252 |
| rs530753214 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886277 | GAGTAAAACAAGAGG[C/T]GGCCTTCACCCTTAG | 11252 |
| rs530753317 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918398 | CTAGAAGTGGGATAA[A/G]CCACCATCCAAGCAG | 11252 |
| rs530756344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962360 | CTTTGGGGGTAAGCA[C/T]TGTTATCTTCATTTC | 11252 |
| rs530762241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882061 | TAGCTATGCCTAAAG[A/G]CTGCCTGATAAACAG | 11252 |
| rs530766956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929857 | GATCAAGATCAGATG[C/T]CACCTCTTTCATAAA | 11252 |
| rs530769663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931751 | TAATTTAACAGAGCC[A/C]TGCAGAGATCACGTT | 11252 |
| rs530783692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925441 | GCCAAGATCACGCCA[C/T]AGCACTCCAGCCTGG | 11252 |
| rs530798433 | snp | C/T | 4.96742e-05 | 0.00498344 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876919 | CGTCCTTCTCACTGA[C/T]GGTGCTGCCCGTGTC | 11252 |
| rs530799256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882666 | GGGTGTTAGAAAGTA[C/T]CCCTCCTTCCTCATC | 11252 |
| rs530824583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014232 | CTGGGGAAACTCTGA[A/G]GAGGGTCACAAGGGC | 11252 |
| rs530834538 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871141 | GCGGCTATTTCTGTT[C/G]TTCTGCGTCTTCCTG | 11252 |
| rs530838211 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889000 | TTGCTTGTCCTGTGC[A/G]TGGTTCGAGGCACCA | 11252 |
| rs530839151 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907998 | CTTCCTGGCAGGGAA[C/T]GGTAAATGTTGAGAG | 11252 |
| rs530844159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912481 | AAACGTGAGTGGAGG[C/T]AATCCCACCTTTGAC | 11252 |
| rs530846486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926011 | GTGGGCGCTCAGGAA[A/G]TAAGGCCCACATTAA | 11252 |
| rs530875010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968786 | GCACTCACCTCCTGC[C/T]TTGGGCCACGGAACC | 11252 |
| rs530881480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994153 | AAGAGATGTCATCAG[C/T]AAAGCCCTAGAGGGA | 11252 |
| rs530891459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962975 | GGCAGCTCTCCTGTC[C/G]CTGGCAGTGATACAG | 11252 |
| rs530906386 | in-del | -/TTAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927573 | TATTTATTTATTTAT[-/TTAG]TTATTTAGTTATTTA | 11252 |
| rs530909532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995560 | TGGAAAAACCAGAGT[A/G]TGTATACAACTACTC | 11252 |
| rs530923571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996176 | AATGAGCCGAGATTG[C/T]ACCACTGCACTCCAG | 11252 |
| rs530929345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907193 | TCAGGAAGAGCCAGG[A/G]AGTCCAGCTGGCTGT | 11252 |
| rs530946232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956327 | TATGACAGAGTCTAA[C/T]AAGAAAAAACTTAGG | 11252 |
| rs530957963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877475 | CTCTTCAGCCCACAC[A/G]GCCTCCTCCTGACTA | 11252 |
| rs530965562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901688 | GCGATCGCCTGACAA[A/G]GCCTAACTTCTTGCT | 11252 |
| rs530965833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907714 | GGGCACTGCTCTGCC[A/G]CCTCCTAACTGCTCT | 11252 |
| rs531008294 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944286 | AGGCTAAGTCTCTGA[A/G]ACTTGGGGTTTGCTT | 11252 |
| rs531008381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872112 | GTTCCATTTATCTTT[A/G]GTTGTTCCAACCTGA | 11252 |
| rs531020407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938218 | GTTGTTTCCTGGGCT[C/T]GCGAAGCAGCAGAAG | 11252 |
| rs531029787 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913236 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG | 11252 |
| rs531102875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902038 | TGGCAACACTCTCTT[G/T]CCACTGAGAGGTATT | 11252 |
| rs531104459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895614 | GGAGCTGCAAATACA[C/T]ATTTACATGACAACT | 11252 |
| rs531160884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965757 | CGATGAAAGGCATGA[A/C]AATGACAGTTCAGTG | 11252 |
| rs531195593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885283 | TGACCTCACACTGGT[A/T]CACACTTCCCCGCAC | 11252 |
| rs531204434 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938586 | GAGGCTGTCCAAACA[C/T]GAAGAATGCCTCTGC | 11252 |
| rs531226536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879972 | TTCTCGGGTGGCGAA[C/T]TGGCTTCACCAACCG | 11252 |
| rs531238410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922620 | GTTTCCTCTTCACTA[C/T]CTGGGGGGAGATTCT | 11252 |
| rs531239438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915883 | GTCAGAATCTAGCAA[A/G]GATATCCGAAGCCCT | 11252 |
| rs531299484 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916595 | ACTCTCCTGGCTCCC[C/T]GCTCTCACCCTGACA | 11252 |
| rs531311981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909908 | TTGACTGTGCACACC[A/G]ACTCCCTCAGCTCCC | 11252 |
| rs531323480 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879471 | AGAGGACCAGCGGGG[A/G]TGGCGAGGACCAGGG | 11252 |
| rs531334707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879846 | CTCAGTCTCCAAAGC[C/G]CAGGGCCCTCCCCAG | 11252 |
| rs531360247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904078 | ACAGAAACCCAGAAA[C/T]TGCAATTTTCAGATC | 11252 |
| rs531371257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910451 | TGAGGCCACAGCCTC[C/T]CTGGGGGGGCCAGCC | 11252 |
| rs531390713 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965541 | GTCTGCATCTGCAAT[A/G]CAGTGGTGACTGACA | 11252 |
| rs531415870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947618 | GCTAGCCTGGATGCA[C/T]AAATCTAGAAGGTCT | 11252 |
| rs531417949 | snp | G/T | 6.62954e-05 | 0.00575702 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888631 | ACGTGTAAAAACAAG[G/T]GTACAGTTTACCTTA | 11252 |
| rs531433667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993099 | GAATCACTTCAACCC[A/G]GGAGGCGGAGGTTGC | 11252 |
| rs531475799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991524 | AGAAGCCTCTGTATG[A/G]CCCAGAGAAGAAGGA | 11252 |
| rs531480878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941410 | TTGAGTAGATACCTA[A/G]GAGTAGAACTGCTGG | 11252 |
| rs531506221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891369 | TTTGCTCTGCCCCTC[A/G]TGTTAGGAAAATTGG | 11252 |
| rs531539241 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000841 | ACATACTGTGTGGCA[C/T]TGCCGTGATCCAATC | 11252 |
| rs531570737 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869276 | TTCCTCAGGGATTTC[A/G]CTCAGTGCTTTGGGC | 11252 |
| rs531628665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898712 | CCGAGCCCAGGACTC[A/G]CCCTGCCGCCTGCCC | 11252 |
| rs531642681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935780 | AAGCAGCACCCTCAG[A/G]CAGCATGAGACCTGG | 11252 |
| rs531652314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930448 | ACGCAGAGCCTAGCA[C/T]AGATGAGGCACCCAC | 11252 |
| rs531700259 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012397 | TGTGGATGGGTATCC[A/C]GGATTAGGGAAAAGT | 11252 |
| rs531705139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979101 | AAGCTCCATTGCCTA[A/G]GAGAAACAGCCAGCA | 11252 |
| rs531737526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893330 | CCCGCTCTGGAACTG[A/G]GAAATGCACTCTTGC | 11252 |
| rs531745916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886339 | AAAGTTCTTTTATGA[C/T]GGATGCTACAAGATG | 11252 |
| rs531787850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923373 | CCTGGCCCGCAGGCC[C/T]GCATCTGCTCACCTC | 11252 |
| rs531820648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972368 | GGGACATAAACATTG[C/T]GGAAGGCCGCAGGGT | 11252 |
| rs531835871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875756 | GGTTAGGCTGGGCTC[A/G]AACTCCTGACCTCAA | 11252 |
| rs531842956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917750 | GTTAGTAAGCCATGG[C/T]GGTTTAATCTGCATT | 11252 |
| rs531866216 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006924 | AGGCCATTCCCACTC[A/G]AAAAGCCCTTCTCAT | 11252 |
| rs531868750 | in-del | -/T | 0.402806 | 0.197864 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898277 | ACCTCCTTCCTTTTC[-/T]TTTTTTTTTTTTTGA | 11252 |
| rs531886264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887045 | GGGCACCTGATTCCC[C/T]GGGATTCTGGCAAAG | 11252 |
| rs531888339 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880526 | CTGAACTGCTAGGAG[A/C]CTAGCGGGGGCAGCA | 11252 |
| rs531916062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955057 | CTCTAAAACTCATCA[C/T]CAAACTGGAGTTTCC | 11252 |
| rs531916115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948184 | GCTGGTCCTGGAGGG[C/T]AAACCCTGGGAAGCT | 11252 |
| rs531922063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994113 | GGAATCCTTCTGATA[C/T]TGCGCCAGAATGCTA | 11252 |
| rs531927429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880798 | AGACAGACTGTCAAA[C/T]AGTCCTCCCCACTGT | 11252 |
| rs531957639 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980467 | AAAAAAACAAACAAC[C/T]CTCTCCCTCTCCCTC | 11252 |
| rs531993562 | snp | C/T | 9.93921e-05 | 0.00704884 | missense | PACSIN2 | GRCh38.p7 | 22:42876227 | AGGTGGCGTCGTCGT[C/T]GAATGGATTCGAGTC | 11252 |
| rs532005842 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953637 | GTGCTAAGGGTTTCA[C/T]TTAACACGAGGAAAA | 11252 |
| rs532020765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938473 | TAGAGGAAAGGAAGG[A/T]CAGTCACAGCAGCAG | 11252 |
| rs532032765 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919903 | AGGTGGATCACTTGA[A/G]GCCACCCTGGGCAAC | 11252 |
| rs532041935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000731 | TAAGAAGAAAAGAAA[C/T]AAATCCAAAAGGAAA | 11252 |
| rs532053757 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009234 | TGTTTGCTCCATCAA[C/T]GTGCTGACCAAGCCT | 11252 |
| rs532118691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895524 | GATTTTCAGAACCAC[C/T]GGTTAAAGGTTTAGG | 11252 |
| rs532149817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942252 | CCCAAGAGTTCTTTA[C/T]GTATTCAAGGTATCT | 11252 |
| rs532157309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896000 | CCCAGGAGCAGAGCT[A/G]CTGCTGGCTGCTTCT | 11252 |
| rs532157365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889732 | GGCTGCAGGCAGGGG[C/T]GGGGCACACAAGCTG | 11252 |
| rs532187670 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943931 | ACCTAAAATACATTA[A/C]GAGCTGATATGAAGA | 11252 |
| rs532196808 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013043 | GTGATCTGCCCGCCT[C/T]GGCCTTCCCAAGTGC | 11252 |
| rs532220334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964134 | TTTACAAGGTGATTC[C/T]TGGCTGGGCACGGTG | 11252 |
| rs532221879 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975451 | CAAAAATAAAAAATA[C/T]ATACAAATATATATA | 11252 |
| rs532256976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996303 | CTTTGGGAGGCCAAG[A/T]TGGGTGGATCACAAG | 11252 |
| rs532294301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890279 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 11252 |
| rs532298963 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921231 | AGGCGTGGTGGCACA[C/T]GCCTGTAGTTCTAGC | 11252 |
| rs532299252 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869829 | TACACATGTAAAGGA[A/C]CTGTTAAACTGAAAA | 11252 |
| rs532299978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958220 | CACTCGGCTACCAAC[A/G]AGACGAGTGACCTTG | 11252 |
| rs532308992 | in-del | -/T | 0.234692 | 0.249531 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007220 | ACACACCTCTTGTTC[-/T]TTTTTTTTTTTTTTT | 11252 |
| rs532321187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009707 | TCATATTCTTGGGAG[A/G]AAAAATAATCATATA | 11252 |
| rs532339030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951289 | TAGACAAGTAATTCC[A/G]GACAGTCCTGCAAAG | 11252 |
| rs532357290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010019 | AGATTATAGGCGCAC[A/G]CCACCATACCCGACT | 11252 |
| rs532365061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872861 | GGAGCAGATGCAGGG[A/G]CCACAGGGCAGCAGC | 11252 |
| rs532370848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951779 | CAACTGTCACAGTTA[C/T]TGATACTCCCCACCC | 11252 |
| rs532427677 | in-del | -/TTTT | 0.457388 | 0.139608 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983965 | CACAGCACTTAGCAC[-/TTTT]TTTTTTTTTTTTTTT | 11252 |
| rs532437717 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015237 | CCGCCCCACAGCCTC[C/T]CCGGCGCCCCCGATT | 11252 |
| rs532440510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914035 | TCCTCCAAAGACATT[A/G]CCGCTGTGAGGAGAC | 11252 |
| rs532446268 | snp | A/C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941029 | AAGAAACCCCACACC[A/C/G]TTCCCCAGTCATCCC | 11252 |
| rs532447289 | in-del | -/TTTTCT | 0.0113151 | 0.0743606 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917791 | TTGGTACTCTTTTCT[-/TTTTCT]TTTTCTTTTTCTTTT | 11252 |
| rs532452257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997242 | TAGCACATGGCAGGC[A/G]TTCAAAAATTTGCTG | 11252 |
| rs532467732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907807 | GCCCAGGGCCCGGGT[A/C]ATGGCAGCTTCTAAA | 11252 |
| rs532471416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985423 | ACGTTCTGCCCACAA[A/G]GGCAGCAGATGGGCA | 11252 |
| rs532475540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976424 | CAGGCGACAGACTGG[C/G]TCCTCTCCCCAAAAG | 11252 |
| rs532522999 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935270 | GTCCAGCAGTGTCTG[C/T]GCCATATTCCTGATT | 11252 |
| rs532537019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976966 | TATGCTATCCTTGCA[C/T]TGCTAGAGTAAACCT | 11252 |
| rs532537143 | snp | A/G | 1.65924e-05 | 0.00288027 | missense | PACSIN2 | GRCh38.p7 | 22:42891137 | ACCCTCTCTGCCTCG[A/G]ACATGAAGGCCATCC | 11252 |
| rs532551319 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945619 | TCTTCTTCCCACACC[C/G]AACCCCCCTCACCAC | 11252 |
| rs532568271 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914137 | CCACACTGGTTAGGG[C/G]TCTGCTCCATAATCA | 11252 |
| rs532575304 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891553 | TTACAGGTGCCCGCC[A/C]CCACGCCTGGCTAAA | 11252 |
| rs532575664 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968842 | TGGACTTATACCAGC[A/G]GCCCCTGGGTTCTTA | 11252 |
| rs532624338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939148 | GCTGGAGCTAACAGC[A/G]TGTAATTAGATGTGT | 11252 |
| rs532640984 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891803 | GGCCAGAGAAGGGGG[C/G]ACCTTCTGAAGTGAG | 11252 |
| rs532680442 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916909 | CTCGGAAATGTTGGT[C/G]ACTGGGGCTGGGTTT | 11252 |
| rs532681174 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017016 | TAGCCAGGCGTGGTG[A/G]CGGTCGCCTGTGGTC | 11252 |
| rs532710552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884841 | TGTATGGTCTTGAGC[A/G]TGCCACACGCCCATG | 11252 |
| rs532732264 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960497 | ACACTCAAATACGCA[A/G]CTGTGATTACATGGA | 11252 |
| rs532732451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971541 | GCGTCTCTGCCTGGC[A/C]GCCCATCGTCTGGGA | 11252 |
| rs532747165 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869445 | ACACAGTAGGTGCTC[A/G]GGAAAATGTGCTCAT | 11252 |
| rs532784165 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870042 | CACGTTCCCCCCACC[A/C]CCGCCGGCCCGCGTG | 11252 |
| rs532790231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948127 | AGGTAGAGGAACCTG[C/T]GTGACAAAGGGGAGT | 11252 |
| rs532791712 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885723 | GACCAGGTTCCACCC[C/T]GCCCTCTAGGGCCCT | 11252 |
| rs532802602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934363 | GTGTGTGTGCAGATC[A/G]CCTTTTCCCTTCTTT | 11252 |
| rs532820907 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971146 | GCCGAGCCAAAGCTG[G/T]ACTGTACTGCCGCCA | 11252 |
| rs532861338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921910 | TGCCAGGCTAATTTT[C/T]GTATTTTTAGTAGAG | 11252 |
| rs532865058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979251 | ATATTTGGCCAGGTG[A/C]GGTGGCTCATGCCTG | 11252 |
| rs532867108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007162 | GAGAATATAAGGCAG[C/G]TCATAACCTGGAGCC | 11252 |
| rs532867305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987897 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCG | 11252 |
| rs532872657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928972 | TTCAACAAGCTCTTA[A/G]AGTTCTCTGAGTTTA | 11252 |
| rs532878859 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872794 | TCAGCCTCCCACTGT[C/T]GTGCCGCTTCTGCCA | 11252 |
| rs532882373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964829 | CCGAGATCCTACAGG[C/T]TGGCCCAAGCCAGGG | 11252 |
| rs532884160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905233 | ATGATGGCATTCACA[C/T]GGGGGGAAGACAGGT | 11252 |
| rs532913225 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913600 | AGTAAGTGCTACGAA[A/C]TTACTAAGTACTGTT | 11252 |
| rs532920665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899893 | ATACGTGCACATGAA[A/G]TAGGGGTGCGAAGTT | 11252 |
| rs532999824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886278 | AGTAAAACAAGAGGC[A/G]GCCTTCACCCTTAGG | 11252 |
| rs533007821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948725 | CTATGCACTCAACTA[C/T]GGTGCCGCTTTCTCA | 11252 |
| rs533015762 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892039 | GAAGCCCATCCTGCA[A/G]GAGGAAGGAGAGGAG | 11252 |
| rs533034032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931185 | CCACGGCTGGGCACA[G/T]CACCTGGCTTACACG | 11252 |
| rs533037689 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893323 | ATCACACCCCGCTCT[-/G]GAACTGGGAAATGCA | 11252 |
| rs533041199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994068 | AGCCGAAATCAAATA[C/T]GAGCTCTCAAGAAGA | 11252 |
| rs533054404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973360 | TTGCTCAGGAATTGA[C/T]GAGCAAAACACAGGT | 11252 |
| rs533094924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924713 | AAATGGTCTCCCTCC[A/T]GCCCCACAGGCCTGT | 11252 |
| rs533124328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900485 | AAATTAAATTAAATT[G/T]TATTATTTTATTTGC | 11252 |
| rs533129912 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013602 | ATTCAACACTGCCTG[C/G]CTGGTCGGTTCCCTT | 11252 |
| rs533137482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935951 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11252 |
| rs533141881 | snp | A/G | 1.65627e-05 | 0.00287769 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888805 | TGCTTCTACCTACAG[A/G]GAGAATGAGTTCCTG | 11252 |
| rs533156875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881524 | CAGCTGACGCCACGT[A/G]CTTAAGCCTCAGGGG | 11252 |
| rs533205346 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929364 | CAGCAATTAATATTT[G/T]TATCTTGCAAAACCA | 11252 |
| rs533222966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001536 | AGCTGGGCAGCGCCT[A/G]GCAGAGCCAGTGCAG | 11252 |
| rs533254990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912400 | ATAAAAGGCAGAGTC[C/G]TTGGATCTCTGGGCT | 11252 |
| rs533314822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913167 | ACCCTCTCTGTGCCT[C/T]GCTTGCCTTATCTGG | 11252 |
| rs533322725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906520 | GAGGGCCCTGATCTG[C/T]CCCATAGGACGACAA | 11252 |
| rs533328481 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879819 | CTGACAGAAGGGGCA[A/G]GCAAGCAGACTCTCA | 11252 |
| rs533340401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975268 | AATCCATTAGAGAAA[A/G]TCCCCATTCTTGTGG | 11252 |
| rs533360016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949751 | AACCTGTCCTTCATA[A/G]AAATTTGTCAGTTTG | 11252 |
| rs533384673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881967 | AGAGGACATAACCGC[A/G]ACTTCAGGAGAGGTT | 11252 |
| rs533393006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925299 | AGCCTGGCCAACATG[A/G]TGAAACCCCATTTCT | 11252 |
| rs533414534 | in-del | -/T | 0.499801 | 0.00998203 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942100 | GAATTTTAAGAGTTC[-/T]TTTTTTTTTTTTTTT | 11252 |
| rs533526897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956043 | ATTACATCAACATTT[C/T]GTCAAGTAAGCATTT | 11252 |
| rs533572385 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877347 | GGGCTTCTCCTCTGT[C/T]CTGACTCCCACCAAT | 11252 |
| rs533577409 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958463 | ATAAATCTCATACCT[A/C/G]TAAAAATGCTTTGGT | 11252 |
| rs533613446 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934977 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 11252 |
| rs533653003 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908623 | CTCTGACTTGCTGAG[A/G]GAGCGACCCACCTGG | 11252 |
| rs533660254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989855 | ACTCATTCTCTTGGA[C/G]GGGGAAAAAAAAATA | 11252 |
| rs533668399 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999864 | TATTTCCTCAACTGT[A/T]AAGTGGGAATCAAAG | 11252 |
| rs533674150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907116 | CACCAGGCAGGGTCA[C/T]AGATCTTTGTGGATG | 11252 |
| rs533677401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952038 | TCTTAAGAAAGCCTT[C/T]CCCCAGCCCTGATAC | 11252 |
| rs533684248 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959102 | GGGTCCAGCTGGGAT[A/G]AGAAATGAGAAGAAC | 11252 |
| rs533717735 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959077 | GCCCTCAGAGGGGGA[C/T]GAGGGCACAGGGTCC | 11252 |
| rs533725879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945864 | GGTGGTTGGAATGTC[C/T]TCTGGAAAGATCAGG | 11252 |
| rs533736339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878425 | TTACTGAGTGTCACA[C/T]GGAGGCCTGTGGGCA | 11252 |
| rs533744048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957818 | TGTTTCTTGTATTAG[C/T]TGTGATTGTATTAAG | 11252 |
| rs533776034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872397 | GTCAGGAGCAAGCAA[C/T]TGGTGGGAAAGAAAT | 11252 |
| rs533799418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940194 | AAAACCAAGTGGAAA[A/G]CATGCACGGGCTTAA | 11252 |
| rs533805314 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927160 | ATGGACTGACTTCAC[C/T]GTCCTTGCAGCCAAC | 11252 |
| rs533827243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990779 | ACAGTCCGACCCCTC[C/T]CCGTTGCCAATAAGA | 11252 |
| rs533846498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977252 | TGTAAAAACAAACTA[C/T]AGAAACAATAGCTGG | 11252 |
| rs533854211 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005500 | AGAAAGACAGGCCCT[A/G]TAAGTGCCAGGATAT | 11252 |
| rs533870302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907951 | GAAACCAGCCCGACT[C/T]AGAGCAAGTTGCAAC | 11252 |
| rs533893226 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991406 | CAGCCTGAGCCCCAC[C/G]CCACCCATCCAGGCA | 11252 |
| rs533906503 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971279 | TTTGGTGGAGACGGG[G/T]TTTCGCCGTGTTGGC | 11252 |
| rs533917762 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872934 | CCCCTGGCGTTTCTT[G/T]TGTCCTGCCTTCATT | 11252 |
| rs533938205 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933122 | CATATTCAGAACCTA[C/G]TCTATTATTATCTTT | 11252 |
| rs533951453 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884956 | AATCCTGCAGCTCTC[C/T]TGGAGCCTCACTGTC | 11252 |
| rs533970128 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001299 | GATGACCAGAGGCTT[C/T]CATGAAGCCCCTGCC | 11252 |
| rs533993830 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879227 | CTTGCTGGAAGCCAC[A/G]TCTGTCCTCAGTTCC | 11252 |
| rs534004336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965095 | AGCTGAAAACCACTC[A/G]GCAATAAAAAGGAAT | 11252 |
| rs534029487 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999731 | GATGGAGCAGTCCCC[C/T]GGCAGTCACTCCCTA | 11252 |
| rs534032792 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900649 | GGCTAATTTTTTATA[-/TT]TTTTGTAGAGACAGG | 11252 |
| rs534058290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934226 | TTTGAATAAAAACCA[C/T]ACTAAATTCAAAACA | 11252 |
| rs534066258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959309 | AATGGCAGCATGTAA[C/T]AAACATTAACGCCTT | 11252 |
| rs534071778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985523 | CAGGAGTGTCACCTT[C/T]ACAGCACCTAGGTGC | 11252 |
| rs534083124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976620 | AGATTAGCGGCAGAA[C/T]TGTATTACATGCCTT | 11252 |
| rs534104423 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016180 | CCCAGTTCTCTAAAA[A/T]GTAAAATAAAAGAAA | 11252 |
| rs534113318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922828 | TCCTACTAGGGCAGA[C/T]TGGCACACAGCAAAG | 11252 |
| rs534118345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898125 | GAACCCAGGGCATGC[A/G]AGCCAAAAAAGGGAG | 11252 |
| rs534153047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953160 | AAGTTGAGAGGGCAT[A/G]TGGAGTTAAAATGTT | 11252 |
| rs534156282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891756 | AAAAACTCAAATTTC[C/T]ACATCTTAGAAGTCT | 11252 |
| rs534177175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927810 | CAGGCTGGTCTCGAA[C/T]TCCAGACCTCAGGTG | 11252 |
| rs534199057 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974738 | TGGGCAACACAGTGA[A/G]ATCTTGTCTCAAAAA | 11252 |
| rs534234407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010996 | ATGATGTATTGTGCA[C/G]AATAATTTGAGAATT | 11252 |
| rs534235033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986366 | CCAAAGAAAACACTC[A/G]TGAGTATCAATCAAG | 11252 |
| rs534240794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922210 | TAACAGAGGTTGCTA[A/G]GGTGACCGTGGCACA | 11252 |
| rs534270606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011590 | CGCCCTTAACACAGC[A/C]CAGACTTTCAAGGTA | 11252 |
| rs534275153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887504 | CCCCTCTGCCCATGT[C/T]CTCTTCCTGGAGTGC | 11252 |
| rs534282360 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945840 | ATGACATTACTGTGA[C/T]TCTACCATGGTGGTT | 11252 |
| rs534294226 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967485 | CAACCCCAGAATCAA[A/T]GAAAAGCCTTAAACT | 11252 |
| rs534298896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930950 | GCAGAGGTGAGTCAC[C/G]TGTGCGTGACTCTGA | 11252 |
| rs534304579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916113 | TGAACCCCAGTTCCT[C/G]AGCTGTGCTTTACCA | 11252 |
| rs534380124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972731 | CCTCACTCTAAGAAA[A/T]GTCAGCCATGCTTTT | 11252 |
| rs534380891 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998027 | TTTCCTGGAAAAGAG[G/T]TTTCTCAGGAGCCAG | 11252 |
| rs534387514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880075 | CCGCAGGTGTTTAAT[A/G]AGCTCTCCTTCCCCC | 11252 |
| rs534403392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007697 | CAGTACTTTGTACAC[A/G]CTACTATCTGGTACC | 11252 |
| rs534433810 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909667 | GACATTATTGCAGTT[C/G]AGAATTTAACAGGGA | 11252 |
| rs534461255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961901 | TTATTTACCACCCCT[C/T]CCCACACAGCCCGTC | 11252 |
| rs534470793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962484 | CTTGACTTCCCTCAA[C/T]GGTCAGAACTGGGTC | 11252 |
| rs534476407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876603 | CCAGCACAGACTGCG[C/T]GTTGTCTGTTTTCCT | 11252 |
| rs534524923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993215 | CATAGAATACATACT[A/G]TATGATTCCATTTAC | 11252 |
| rs534550561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894303 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 11252 |
| rs534550765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994422 | GTGTCCTGCGCCACA[A/G]AGACCCTCGGGCGTG | 11252 |
| rs534562004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995005 | CTGGAAATTCCATTT[A/G]GGCTGCCTCCTGGAC | 11252 |
| rs534619496 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989526 | AAAAGGCCAGGTGTG[C/G]TGGTTCACACCTGTA | 11252 |
| rs534621502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995614 | CCAATGTCATTCACG[C/T]GGCAATTATTTGGAA | 11252 |
| rs534640893 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871157 | TTCTGCGTCTTCCTG[C/T]GCTCAGATCCCTCCA | 11252 |
| rs534662645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901431 | CTTGTTCAAATCCAT[C/T]GGATTTCCCAGCCCT | 11252 |
| rs534671746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907372 | TGATGCCTTAATCCT[C/T]GCTCATGGTTCAGCA | 11252 |
| rs534681267 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970688 | TTCTTTTTAAAATTT[A/T]GCCAAGGAAGATGAA | 11252 |
| rs534683682 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995107 | CTGCTCCGGGCCCCA[A/G]CTGCCAGGAAGCAAG | 11252 |
| rs534684010 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966465 | TCAAAGAAGAAGGTC[C/T]CAGGACAAAGCAAAG | 11252 |
| rs534699904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950686 | AAGCTGAACACTTGG[A/G]CTTTATCTAAAAATA | 11252 |
| rs534723050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925564 | GCCCCAGCATCCAGT[A/G]TCAAACACAAAGCAG | 11252 |
| rs534723201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918977 | GTCAGGTAGGGCATG[C/T]TTCCTGGCTCTGCTT | 11252 |
| rs534790191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895206 | AGCTCCTGTGAGGAA[G/T]TCGGAAGTGAGCATT | 11252 |
| rs534806972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909610 | AAGCTGAGCAGAGCC[C/T]GCCTGAGCATTTTCA | 11252 |
| rs534826692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895772 | TGCTGGGGACAAGAG[A/G]CAAGTTGGCTGAGCA | 11252 |
| rs534839070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919503 | ACTCAGGCTGGGCGT[A/G]GTGGCTCACGCCTGT | 11252 |
| rs534840453 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922980 | TGGGCAGTGGGCATG[A/G]GAAGGACAGGGGAGG | 11252 |
| rs534850223 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014929 | CGCGGCGGCCCTGAC[C/G/T]GGGCGCGGGCCCGGC | 11252 |
| rs534861494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001658 | TTATGTCTACCTTCC[C/T]GGGTAGTCAAGTCTC | 11252 |
| rs534904883 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014100 | GAAACCCAATGAATC[-/A]ATGAAATTCAACAGC | 11252 |
| rs534907383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912537 | TACCACATTCCACTT[A/G]TGTGAGCACTGTCCC | 11252 |
| rs534909358 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874313 | TAACAGAGTGAGACC[A/G]TGTCTCTATTAAAAA | 11252 |
| rs534911194 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901628 | GAGGGGTTTACACTG[A/C/T]ACGGTAGGTTTCTTC | 11252 |
| rs534933476 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015375 | TGGGCTGCGAGGGTG[A/G]CGCAGATTACTCTCC | 11252 |
| rs534941676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920320 | CAGAAGCATGCCATC[C/T]GAATTCCAACAAGTG | 11252 |
| rs534945894 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950120 | CATCTGTACTAAACA[G/T]GTACAGACTTTTTTT | 11252 |
| rs534950804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933440 | GTGGAAGCCTCAATT[C/G]AAGTCCAAAAATAAA | 11252 |
| rs535000410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920773 | GCAGGGGTGAGGGTC[A/G]ATTATCATGAATTAT | 11252 |
| rs535017167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944437 | CCAGTTTTGGTGGGG[C/T]TACAGGAAAACAGAA | 11252 |
| rs535018775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937635 | TGTGAGTCAGCATAC[A/G]AGGTGCTTTCACTTA | 11252 |
| rs535035474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883780 | GAAGGCCGAGGTGGG[A/C]GGATCACAAGGTCAA | 11252 |
| rs535060073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916450 | CTTGAGGGCAGGCAC[A/C]GAGCTGAGTTCTCAA | 11252 |
| rs535076525 | snp | A/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945047 | AGGTTGCGGTGAGCC[A/G/T]AGATCATACCACTGT | 11252 |
| rs535099597 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896171 | TGTGCCCCCTTGCAG[C/G]CCATCCCCTCCCCAT | 11252 |
| rs535111922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992800 | AAACTAACTGATAAA[G/T]GCTACAACAATCTCA | 11252 |
| rs535118879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903708 | AAATGAGGTGATGCT[A/G]TTTACCTTGCAGGGC | 11252 |
| rs535167740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975986 | AGACACCCTGGCCCC[C/T]ATGGCTTTCCAGGCC | 11252 |
| rs535167862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940843 | GCCAGGAGAGGCTGT[A/G]GGAGGGATGATGGGT | 11252 |
| rs535191004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898733 | CCGCCTGCCCTCCTC[C/T]AGGCTGCACTCACTC | 11252 |
| rs535191719 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889937 | AAAAAAATAAAGTGA[A/C]AGCAAGTTTATTGAG | 11252 |
| rs535193929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986341 | GCTGTTTGGAAAAGC[A/G]CAGCGGCCCCCAAAG | 11252 |
| rs535203291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003053 | TTCCTCACATTCAAA[C/T]TAACAACCTCGAAGT | 11252 |
| rs535263466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926446 | CCATCACCGAAAACC[A/G]GAGGATTTCAAACCA | 11252 |
| rs535289266 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927185 | GCCAACAAGCCATCC[C/T]GTGTTCTGCTTTCCT | 11252 |
| rs535318327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922866 | AGCTATATGGTGTGA[A/G]AAGCACCAGGACACA | 11252 |
| rs535321514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970036 | TCACAAAATCACAGA[A/G]CCCAAATGCATCTCC | 11252 |
| rs535326274 | in-del | -/CG | 0.0562307 | 0.157967 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949456 | AGCCTCATACACACA[-/CG]CGCGCGCGCACGCAC | 11252 |
| rs535345389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012118 | CCACTGCCTCCAGCC[C/T]GGGCGACAGAGCGAG | 11252 |
| rs535375168 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885636 | TCTGACTCACGTGGC[G/T]CAGAGCCCTGGGAGA | 11252 |
| rs535381350 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966297 | ATTGCTTGAACCTGG[A/G]AGGCGGAGGTTGCAA | 11252 |
| rs535382563 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878286 | AGACAGCGTGCAAAG[C/G]AGCGGAATGACGACA | 11252 |
| rs535385531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877927 | GAACCAAGGAAGGGA[A/G]GCGAGGACATGCCTC | 11252 |
| rs535389883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963824 | AAAGGTCGTGTCATT[C/T]GGAAACAATAAAATT | 11252 |
| rs535434169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946695 | CTTCACACAGGCATG[C/T]GCACACACATGATCC | 11252 |
| rs535441720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945551 | TTCCTGGGTTTTCTA[C/T]GTCAGAAATGGTCCC | 11252 |
| rs535448489 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947218 | TAGGGGCATTCACAG[C/G]CGGCAGAGTGAGCAG | 11252 |
| rs535466356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985693 | GTCATCCAGCTCCAG[C/G]TGGTTTTTAACCTTC | 11252 |
| rs535508007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917198 | AGGGTTGGAGCTTGC[C/T]CAAGCAGCGGAGTTG | 11252 |
| rs535516685 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924828 | GTGGCACGATCTCAG[A/C]TCACTGCAAGCTCTG | 11252 |
| rs535518561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917888 | CCTCAGCCTCCCAAG[C/T]AGCTAGGACTACAGA | 11252 |
| rs535551622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892117 | CCTCTCCCTACTCAC[C/T]GTTCTCAGTCCCCGA | 11252 |
| rs535581422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947850 | GGACCTTCCACAAGC[A/G]TTGGCCAGGGAGAAG | 11252 |
| rs535618983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971783 | CCGCCCGGCCAGCCG[C/T]CCCATCCGGGAGGGA | 11252 |
| rs535632198 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944009 | ACAGAAGAGGAGATG[A/G]CTGGGCAGAGACAGG | 11252 |
| rs535642366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941846 | CAGTGGCGCATTCTC[A/G]GCTCACTGCAACCTC | 11252 |
| rs535662559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901727 | TCTTCACCCTGTCTG[C/G]GGGTCAGGGTGGGGG | 11252 |
| rs535663389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993254 | TTAGAAAATGCAAAT[A/G]ATTCTACAGTGGCAA | 11252 |
| rs535681643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935308 | ACCTGCCTCCTCCCT[C/G]TTTCCCTTTCCCCTG | 11252 |
| rs535685619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011658 | GAGGCGGGCAGATCA[C/T]TGGAGGTCAGGAGTT | 11252 |
| rs535693263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930043 | ATGGAGTTTATTTTT[C/G]TGTCCCAATCCTAGC | 11252 |
| rs535701354 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990763 | AGAATTTTAATCTCA[C/G]ACAGTCCGACCCCTC | 11252 |
| rs535709216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005696 | GGCAAATTCACTTAC[A/G]TAGACTGATAGGAGA | 11252 |
| rs535717210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942757 | TTCTTGACTCTATCT[C/T]ATTTTTCCATGTCTA | 11252 |
| rs535754687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916886 | CCACAGCAAGCCACC[C/T]GAAGGTACTCGGAAA | 11252 |
| rs535767018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886423 | GTATGTATGTAGGTA[C/G]GTAGGTAGGTAGGTA | 11252 |
| rs535784073 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875995 | TGCTTTTGACAATGA[A/G]GCCAGGGCACTGGGG | 11252 |
| rs535784451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972850 | ACAGATGCATGCCAC[C/T]GCACCCAGCTCAACC | 11252 |
| rs535788382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893707 | AACCAGGCCCTGATG[C/T]GCCCCTGGGGTCATG | 11252 |
| rs535796685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966457 | ATTCTCTATCAAAGA[A/T]GAAGGTCCCAGGACA | 11252 |
| rs535817297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880552 | CAGCACACCCACCCA[C/T]GCGGGCCACAGACAC | 11252 |
| rs535855158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875392 | TTTGTTTGTTTGCGA[C/T]AGGGTCTCGCTCTGT | 11252 |
| rs535900492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999890 | CAAAGAGTCCCAAGG[C/G]AAGATGGTTGGCAGG | 11252 |
| rs535949012 | in-del | -/AG | 0.493477 | 0.0567349 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919797 | AAAAAAAAAAAAAAA[-/AG]AAAGAAAGAAAGAAA | 11252 |
| rs535969416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911313 | TACTCAGTAGGCTGA[A/G]GTGGGAGGATGGCTT | 11252 |
| rs535973500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954487 | TGCAGCCTCAACCTC[C/T]TGGGTGTAAGCGATC | 11252 |
| rs535974491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993798 | GGAAGGGCGGCACCA[C/G]GGACAGCCATGTGCG | 11252 |
| rs535995906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957746 | AATGCTAAAGGTTTG[G/T]GGTTTCCCTTTCACA | 11252 |
| rs536014894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929499 | GAAATGTTCAGTGGG[A/G]GTGGCGTGCCTACGA | 11252 |
| rs536023806 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870179 | CGACGACTGAAATCT[C/G]CAACTACTGCAAAGA | 11252 |
| rs536032631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944625 | CACTGCAATATTTAT[A/G]ACAGCAAAAATTGGA | 11252 |
| rs536032673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951378 | CTCTTCTCTGTGCAC[A/C]CTAGTTTCCTGGGTG | 11252 |
| rs536042788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945154 | CCCCAGTGCTTAGCA[C/T]GAGGTAGATGCTCAA | 11252 |
| rs536084706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905393 | GGGAGTCATTTAGAC[G/T]TGGCCTTGCCATGCA | 11252 |
| rs536090418 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987690 | GTGCGCACCACCACA[A/C]CCGGCTAATTTTTTG | 11252 |
| rs536151773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988146 | TGGCTCAAAAACAAA[A/G]TAAATAAATACATAA | 11252 |
| rs536154208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976003 | TGGCTTTCCAGGCCA[A/G]TCTGGAAGGTCCAAT | 11252 |
| rs536214369 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976535 | ATGGCCACTTAACAG[G/T]CTTGCTGCTGGGTGT | 11252 |
| rs536218020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883116 | TGCCTGTATTAAAAG[A/G]GGGAAATCCAGACAC | 11252 |
| rs536220665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970208 | TTAAAAAGGAGAACG[A/G]CTAAAGTAAACCCGC | 11252 |
| rs536256151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877884 | AAAGCACTGGATGGA[C/T]TGCTCAGCCTGAGCA | 11252 |
| rs536265232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956696 | CAGAGGTGGACATGA[A/C]AAAGGCCCAAACACC | 11252 |
| rs536291976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920285 | CTCACGGGCTACCCT[A/G]GGTGCCATGCAAGAT | 11252 |
| rs536296963 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015244 | ACAGCCTCCCCGGCG[A/C]CCCCGATTGGGCCAG | 11252 |
| rs536306071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913453 | CATTGCACTCCAGCC[C/T]GGGCAACAAGAGCGA | 11252 |
| rs536311477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995830 | GCGCTCTGGGAAGCC[A/G]GGACAGGAGGATCAC | 11252 |
| rs536330076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970737 | ATTTGTTAAAATCTT[G/T]AAGTAAGCAAGCACC | 11252 |
| rs536333825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995817 | ACCTGTAATCCCAGC[A/G]CTCTGGGAAGCCGGG | 11252 |
| rs536340358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883873 | GCTGGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 11252 |
| rs536354357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907585 | GGCAGGCCATCACAC[A/G]GAAAAGTCCGTTGGG | 11252 |
| rs536357146 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986922 | CTGCCTATATAATAA[A/C]GCCCCTAAGATCCCC | 11252 |
| rs536374464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996396 | AATTAGCTGGGCATG[A/G]TGGCACACGCCCGTA | 11252 |
| rs536405604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964989 | GCTGCTGAAAGATGG[C/G]GAGGGCATGCACACA | 11252 |
| rs536413787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010922 | ATGTCAAAACTTGTG[C/T]TCTTTGGTGGCCACT | 11252 |
| rs536416825 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984315 | CTTCCTGCCCTCAAT[G/T]AAAAGAAACAACTAT | 11252 |
| rs536434294 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964324 | TCGAGAGGCTGAGGC[A/T]GGAGAATTGCTTGAA | 11252 |
| rs536466553 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911763 | CAAGACCTTTCATAA[A/T]CACCCCTAACCTCTT | 11252 |
| rs536507612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915904 | CCGAAGCCCTAAGGC[A/G]ACACTGAGGCAAGAT | 11252 |
| rs536511368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942646 | TCCAGTTGTCCCAGC[A/G]TCACTTGTTGAAAAG | 11252 |
| rs536514186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938744 | CTGGAGCTCCACGAG[A/G]GAAGGGCTTCACCCT | 11252 |
| rs536525813 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922760 | CACTCTTCTAAGCTG[C/G]GGGAGGGGCAGTGGA | 11252 |
| rs536561189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896499 | ATTCGATTGGGTAGT[C/T]ATACCACTCTTTGGT | 11252 |
| rs536568211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909563 | CTGCGGAGTTGATAC[A/C]AGCTGGAGAGTAATT | 11252 |
| rs536569049 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992092 | TCAGACAGGGAGTCA[A/G]TATTTTCAAATTATG | 11252 |
| rs536582434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874099 | CCGGACAAGATAACA[C/G]TTTTCAAATTGAAGA | 11252 |
| rs536598750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890729 | CAAAAAATAAAAATA[A/G]AAAATTTAAAGAATG | 11252 |
| rs536607565 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015456 | GTTTTGCGGTTTCGT[C/T]GGCATCCAGGGGTAA | 11252 |
| rs536627357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933673 | ACTCAAACCCCAACG[C/G]GGCCCTCACAGCCCC | 11252 |
| rs536688246 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016106 | GCTTCTTGGGACGCC[A/G]AGGCAGGAGAATCGC | 11252 |
| rs536799690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964413 | ACAGAGCGAGACTCC[A/G]TCTGGAAAAAAAAAA | 11252 |
| rs536826967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921737 | GGAAACTTCATTTAG[A/G]AGCTTTTTTTTTTTT | 11252 |
| rs536828648 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007139 | CTCCCCAGTGAACTG[C/T]CCTCCAGGAGAATAT | 11252 |
| rs536850611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881606 | CAATCCAAGGGCTAG[A/G]TGAGTCCTGAGATCC | 11252 |
| rs536853846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952223 | AAACACAACTAGAAT[G/T]AATGAGTCAAGGAAT | 11252 |
| rs536855534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873248 | TACAAAATTACTGTC[A/G]AACCCAATAGGCAGG | 11252 |
| rs536893018 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939082 | GCCCCAAGGTCACCC[A/G]TCCCAGCGCAGCCCA | 11252 |
| rs536895646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918045 | ACTTGCCTGGCAGAA[C/T]CGTGGTGAGGGTCAA | 11252 |
| rs536900828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915186 | GATTTAAGAGCCCAC[C/T]AAGTGCCAGGAGCCA | 11252 |
| rs536907210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000930 | AAGGCCCTGCTTTTG[C/T]GTGACTCTCAGGCAA | 11252 |
| rs536942168 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889312 | GGAACCCAGCATGAG[A/G]GAGAGGACCATACTA | 11252 |
| rs536975167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952637 | GCTGGGATTATAGAC[A/G]TTGAGCCACCACACC | 11252 |
| rs536984834 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914420 | GTATTTTTTAGTAGA[A/G]ATGGGGTTTCCACCA | 11252 |
| rs536985635 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870251 | AGGCCGGTCAGAAGC[C/T]GGACCAGCAGTCAGC | 11252 |
| rs537038701 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015560 | TCCTCTCCCAAGGGA[C/T]TCAAAGAAGCTAATG | 11252 |
| rs537043823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942161 | AGGGTCTCATGTTGC[C/T]CAGGCTGGTCTCAAA | 11252 |
| rs537083204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994926 | CCATCCCACCCCAAG[C/T]CCCAGTCTCTGTCTC | 11252 |
| rs537087704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906090 | GCTGAAAACTGTCCA[A/G]GGGAAATGGCAGTCA | 11252 |
| rs537095109 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870983 | ATGTAAGCTTGTTCA[C/T]TTAAGTTGCAGGTGA | 11252 |
| rs537126825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906688 | AAGGTAGGTATACAG[C/T]GCTCTGAAGAGCAGG | 11252 |
| rs537126919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900930 | CAACATGAGATGATG[C/T]GTGTGCTTCCAGCCA | 11252 |
| rs537140399 | snp | A/G | 0.000222879 | 0.0105541 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893650 | GAGGCAGGGGGCTTG[A/G]GGCAGCCTGTCCTTG | 11252 |
| rs537143668 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980438 | GCCTGGGCGACAGAG[A/C]GAGACCCTCCCTCAA | 11252 |
| rs537149725 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964644 | CACAGGGCAGGCTCT[A/C]CAGTTCCTATGTACC | 11252 |
| rs537182651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936835 | AGAATCACCTGAACC[C/T]GCGAGACGGAGGTTG | 11252 |
| rs537260923 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954741 | AAGACCAGGAAAGAG[G/T]AATATATCCAAGAGG | 11252 |
| rs537270489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961701 | TCGCTTGACCCCAGG[A/G]AGCAGAGGTTGCAGT | 11252 |
| rs537289919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013991 | GTTATACGTCAAAGG[C/G]TGCAGCCGTGTGGGC | 11252 |
| rs537311961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918829 | GTCAGGAAGTACTAC[C/T]ATAATTTTTTTTTGA | 11252 |
| rs537321380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925820 | TGCCTGTCTACCACC[A/G]GCCTCACGGGAGGCC | 11252 |
| rs537321694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932513 | CTGACAGCGACACAC[C/T]TGGGGATCTTTACAA | 11252 |
| rs537331638 | in-del | -/TTTG | 0.00159617 | 0.0282053 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016905 | CTGTAATCCTAGCAC[-/TTTG]GGAGGCCGAGACGGG | 11252 |
| rs537373535 | snp | A/G | 0.000216171 | 0.0103942 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912110 | AGGGAGCAGCAAAGT[A/G]TACTTAGTCAGGGGT | 11252 |
| rs537374282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889869 | GGGATAAAAACCTAT[A/G]CAAGAGAAAGAAAAA | 11252 |
| rs537387434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955321 | AACGAACGAACGAAC[A/G]AAAAAACAAATCAAC | 11252 |
| rs537388728 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962714 | CAGCCTGGATGCCTG[C/G]GGTGGGTGGAGGCAT | 11252 |
| rs537399364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949164 | AATAATAGGTGCACA[C/T]TTTAACTTCTAAGCT | 11252 |
| rs537401073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876459 | CCTTCCGAAGGAGCA[C/T]AGGTGGAGCCAGTGC | 11252 |
| rs537409391 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890242 | CCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 11252 |
| rs537428795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873143 | AGGAAAGCTTTCACA[C/T]TGTGCAAATGTGAAC | 11252 |
| rs537462239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949888 | ACAAATTATTTTACA[G/T]CTATCTCTCCCAATA | 11252 |
| rs537479825 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874704 | CATATGGGGGAACCT[G/T]GTGGTCCTGGCCAAC | 11252 |
| rs537480874 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908791 | TTCCAACCTGGAATG[C/T]CATCCCTTCTACTTG | 11252 |
| rs537500849 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914887 | TGACTGACTGACAAA[A/G]CGTCTTGTCTGTCAT | 11252 |
| rs537520821 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966339 | CCCTGCACTCCGGCC[C/T]GGCGACAGAGTGAGA | 11252 |
| rs537542260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909534 | CGTCATGGAGAAGGC[A/G]GACGACCACAGCACT | 11252 |
| rs537542685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992009 | CCGTAAAAGAACAAA[C/T]TGACTTCAGCAAATG | 11252 |
| rs537553347 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989457 | GAGCCGAGATCACAC[C/G]ATTGCACTCCAGCCT | 11252 |
| rs537576957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946616 | AAGAAGCCCCAGTTA[C/T]ACAACACACAAAGCT | 11252 |
| rs537590101 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937438 | ATGCATGAGCTTAAA[C/T]GGGCACCGAAGACAA | 11252 |
| rs537638560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940232 | AACTCCTTAACTACT[C/T]AGTAATTAGGATGTC | 11252 |
| rs537647176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937505 | CACCAAAGTCCACCT[C/G]TGAGCCCCTGCCTAG | 11252 |
| rs537716777 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959372 | AACTCAAGTAACTCA[C/T]TTAGCTACTCGGTAA | 11252 |
| rs537726339 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017169 | AAAAAAGAAATACAG[A/G]GCCTCTCCCAAATTT | 11252 |
| rs537756784 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983619 | AAAAGATTGACATAT[A/G]AGAATATATCAATTT | 11252 |
| rs537766747 | snp | C/T | 3.46464e-05 | 0.00416197 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882321 | TAAATCAGAGAGAAA[C/T]GTGGCTCTTTTAGAA | 11252 |
| rs537786504 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974391 | AGCTCCCCTTTGCCA[A/G]TGATTTCCATTCCCT | 11252 |
| rs537787333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969429 | ATTATTACCCTGTTA[C/T]TAGCAGTACCACTTA | 11252 |
| rs537861264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880091 | AGCTCTCCTTCCCCC[C/G]ATCTCCACCAGTTAC | 11252 |
| rs537861716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952563 | GACGGGTTTTCACAT[C/T]GGCCAGGATGGTCTC | 11252 |
| rs537868400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945954 | CTGTAACTACTGCTC[C/T]TCCAGCCTCACCACT | 11252 |
| rs537875576 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908017 | AAATGTTGAGAGTCA[C/T]GTGCCAACTCTTCAG | 11252 |
| rs537897837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922789 | GACAAGGCAGACTGG[C/G]TCCCTGCCCTCCTGG | 11252 |
| rs537928312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959939 | TTGGCTGCCGAGATA[A/G]GGTCATTCCCATACA | 11252 |
| rs537937332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985281 | GCAGTGAGCCGAGAT[C/T]TCATCACCGCACTCC | 11252 |
| rs537949536 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985638 | ATAACAGGACAAAGA[A/C]CAGCCCCTCCAACAG | 11252 |
| rs537964232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897376 | AGTTAACTATTTCTG[A/C]TCTATCAGTTTTGTA | 11252 |
| rs537994598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953276 | AAGGAGCAGGCTGAG[A/G]ATTTAATTTCTAAAC | 11252 |
| rs538001861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874857 | TGGGCATCCGCTTTT[C/T]TTTTTTTTTTTGAAA | 11252 |
| rs538006913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953833 | TGCCCTCTCAGAGGC[A/G]AGCGTGATTGTGTGA | 11252 |
| rs538010384 | snp | A/C | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977328 | TACAAAGAGTTCCTA[A/C]AAATTCAAAACAATC | 11252 |
| rs538083456 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016753 | CCTCTTTGCCACCCA[C/T]AATACCTGTGGACCA | 11252 |
| rs538097122 | in-del | -/T | 0.486369 | 0.162217 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894250 | AGCTGAAGGCAATTG[-/T]TTTTTTTTTTTGAGA | 11252 |
| rs538110021 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986119 | TCCCCAGAATTAACA[C/T]AGAAACAGTAAGCAT | 11252 |
| rs538133258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892034 | GAATGGAAGCCCATC[C/T]TGCAGGAGGAAGGAG | 11252 |
| rs538148692 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965216 | TATGTGGATGAAATT[C/T]GAAACCAAGCAAAAC | 11252 |
| rs538154217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986786 | AGGGGCAGCAGCTAC[G/T]GCATCAACACTTGTC | 11252 |
| rs538156705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978794 | TCTACAAAGCATTTC[C/G]AAAAAGGCTGGTCCC | 11252 |
| rs538174879 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899529 | GACTGGCAACCACCA[C/G]AGAGTGGGAAAGGCC | 11252 |
| rs538188491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941704 | CTTTGAAGAAACGTC[A/G]GTTTAGATCCTTTGC | 11252 |
| rs538210906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879889 | CTGGGACTTTTCCTC[C/T]GTGATCTGAGCACAT | 11252 |
| rs538217376 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994028 | CTTCAGTGGGATTCC[C/T]CCAGGCTAAAGTCCA | 11252 |
| rs538239573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924990 | TCTCGATCTCCTGAC[C/T]TCGTGATCGGCCCAA | 11252 |
| rs538267494 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915363 | AGCAAGGGGAAGGGA[A/C]ATTCTCCGGTTACAT | 11252 |
| rs538286179 | in-del | -/T | 0.386884 | 0.209196 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921740 | ACTTCATTTAGAAGC[-/T]TTTTTTTTTTTTTTA | 11252 |
| rs538289645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005645 | TAAATAGAACTGGAT[A/G]AAATCACTTTGGGCA | 11252 |
| rs538303613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006109 | CTCATGCCTTTATAA[A/G]AAGTACCTGAGAGCT | 11252 |
| rs538324829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962519 | ATAGTTTCTGCTTAA[C/T]AAAAAGCTGAACTTG | 11252 |
| rs538358305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917169 | TGTCAAAGCAAGGAA[A/C]CTGGGGCATACAAAG | 11252 |
| rs538362993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910252 | CAAGCTCAAGGCAGG[A/G]AATGATTGGTGCCAG | 11252 |
| rs538364896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999246 | CATGCTCCCCCTCCT[A/G]TAAGTGGTTTAAGCA | 11252 |
| rs538372313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920238 | CACGTGAGGGAGACT[A/G]TTCCTGCACACACTC | 11252 |
| rs538401378 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933142 | TTATTATCTTTATGT[A/G]TCAGAGGAAAACCTT | 11252 |
| rs538415700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950161 | ATTCCCTAAACAATA[C/T]GGTATAACTATTTAC | 11252 |
| rs538418409 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953813 | ACACACGATAAACAT[A/G]TATGTGCCCTCTCAG | 11252 |
| rs538419172 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875300 | GGTATGCAACACCAC[C/G]CCCAGCTAATCTGCT | 11252 |
| rs538431984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995087 | CCCCCCTCCCCGCCT[C/T]GGGGCTGCTCCGGGC | 11252 |
| rs538432834 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871294 | AGGAGTGGATGCCCA[C/T]GTGGCTGGCTGAGGC | 11252 |
| rs538473580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910639 | TGGCTGGCGACCTGT[C/T]TGGCTGTCACTGCTC | 11252 |
| rs538519401 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904724 | CTTCCACAGCCCCCC[C/G]ATACTGCACTCCAGT | 11252 |
| rs538561649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983663 | GATAGGGTCTTGCTA[C/T]GTTGCCCAGGCTGGT | 11252 |
| rs538571185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990622 | GAATGGCATTTGCAG[G/T]AGACAAGATTTGCAT | 11252 |
| rs538577698 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929969 | ACCTCAGATGGAGGG[C/T]GGTCATCCAGGCATC | 11252 |
| rs538592432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013971 | GAGTGGCATCCCCAG[C/G]TCCTGTTATACGTCA | 11252 |
| rs538596363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968606 | CTGATTTTGGGGTGT[C/G]TCCATGGGGCTGTTT | 11252 |
| rs538603234 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962087 | CTGGGGAAGCAAGTT[G/T]GAGACCAGCCTGGCC | 11252 |
| rs538613215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902305 | GCCATGAGGCCCACG[C/G]AGAGTGAGCTGGGGG | 11252 |
| rs538638868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008421 | ATGACCAGCTAGTTT[C/T]TATATTTTTAGTAGA | 11252 |
| rs538641258 | snp | A/G | 1.65778e-05 | 0.002879 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42882232 | CCCGTGATTGGCTCG[A/G]AACCACCTCAGGTCC | 11252 |
| rs538652880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945128 | AGGCAAGGGCTGTGT[C/G]ATCTCCGTATCCCCA | 11252 |
| rs538673602 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978111 | TTCATTCATCCCACA[A/G]TGAGCACCTACAACC | 11252 |
| rs538673663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925779 | TGGGTTTAGCAACCA[C/T]GGTTGGGGGCTGTGT | 11252 |
| rs538676364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975204 | TATTAGCATGGAGGA[C/T]GCTCCCACCATATTC | 11252 |
| rs538685765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919584 | TTAAGACCAGCCTGG[C/T]CAACATGGTGAAACT | 11252 |
| rs538699699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001784 | GAAACAGCCCCTGTG[C/G]GGAGAGGGTAGACAT | 11252 |
| rs538739364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975815 | ATGTTCCAAAACTTA[C/T]ATATCCATCACCTCT | 11252 |
| rs538786085 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969480 | TTTTCTTCTTATGGA[A/G]GCCTTGGGGAAGAAC | 11252 |
| rs538812239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009938 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAGCCT | 11252 |
| rs538812542 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936339 | TCTCATCTGGCAAAC[A/G]ATCCATGTTGGTTCC | 11252 |
| rs538825753 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970639 | CGAACATTCATTACG[C/T]CCTTTGCAAAAAGGA | 11252 |
| rs538836672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932893 | CTAGAAGTCCACACT[G/T]TCCACACTTTTATTT | 11252 |
| rs538848449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010508 | AAGGTCAGGAGATCA[A/C]GACCATCCTGGCTAA | 11252 |
| rs538849421 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950839 | GGGCCTGTGGGGTCC[C/T]GGGATGGGTAGAAGT | 11252 |
| rs538864745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995733 | TAAAGCACATTCCAC[A/C]CATGTTTTCCTCCTT | 11252 |
| rs538877293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990029 | ATACACACATATGTA[C/T]ATATATGTATATATA | 11252 |
| rs538906924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004192 | TCTGATGGTGACCCT[C/G]TGAAGGCCACTGAAT | 11252 |
| rs538908996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927607 | GTTAGTTATTTTTGA[C/G]ACTGAGTTTTGCTCT | 11252 |
| rs538912150 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901487 | CTCTCATGAGGGGAG[C/T]AGCACAGATCTGGCC | 11252 |
| rs538917370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907444 | AGAAACTTTAGTGAA[A/C]CTAATGTGGGCCACT | 11252 |
| rs538942785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964373 | CAGTGAGCCAAGATC[A/G]TGCCATTACACTCCA | 11252 |
| rs538944393 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901837 | GTCAGACATTCGACT[C/G]TGGTTCCATGGGCTT | 11252 |
| rs538958915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944513 | TACAGAACAAGGCAG[A/G]TAACAGTTACCAACC | 11252 |
| rs538966252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915112 | GGCTCAAGCGTTCCT[C/G]CTGCCTTGGCCTCCC | 11252 |
| rs538981509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895874 | GTCCCTTTAATGAAA[C/T]GGTTGTGTGGTGGCC | 11252 |
| rs539005295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898809 | GTCAGCCAAGCCTCA[G/T]TTTTAAAGTCAGCTA | 11252 |
| rs539047546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938670 | GACAGCCTGGCACAG[C/T]GGCATTCCGGTGTGT | 11252 |
| rs539051587 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887220 | GAGAGGGGTTTCCCA[A/G]AGGATTCTGACACTT | 11252 |
| rs539100037 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015384 | AGGGTGGCGCAGATT[A/G]CTCTCCCAAAGCCGC | 11252 |
| rs539107528 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984145 | TGGCTAATTTTTATG[-/T]TTTTTTTGTAGAGAC | 11252 |
| rs539109454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933609 | CCTATACTCTCAACC[A/G]TGGCGCCTAAAGGGG | 11252 |
| rs539125139 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955825 | CCAAATCAATAGATA[C/T]TGGTGATCAGTCTAC | 11252 |
| rs539126312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970075 | TGGCATGCCCCCTTC[A/G]ACACTGGCACCACAG | 11252 |
| rs539135890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978701 | GCAGACGTTCAGGTG[A/G]ACTCAGATCTGAGAC | 11252 |
| rs539147741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007968 | AATAAAAAGCAGGTA[C/G]TTCCACGGGCAGCTT | 11252 |
| rs539182302 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921252 | TAGTTCTAGCTGCTC[A/G]GGAGGCTGAGCCAGG | 11252 |
| rs539190097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964015 | GCAACCATCACCACC[A/G]TCAAGGGTAGGACAT | 11252 |
| rs539204777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927142 | TTGCTTCTCCCATCA[C/T]CTATGGACTGACTTC | 11252 |
| rs539231184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886612 | CTGGGACTACAGGCA[C/T]GTGCTACCACACCCA | 11252 |
| rs539235349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930088 | GTTAAATATGAATGC[A/C]ATGCTTTTCTCATCG | 11252 |
| rs539268250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920920 | TGATCCTCCCACCTC[A/G]GCCTCCCCAGTAGCT | 11252 |
| rs539361553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934615 | GGTCAACTCCCACCT[A/G]CCTTGCAAGGCCCAG | 11252 |
| rs539378556 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880276 | TTGCCCACGCAGTGT[A/G]GGTGGCAGACTTGGG | 11252 |
| rs539379643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904694 | CTTCCGTTCCCTCCT[C/T]TTCCCAGTTTGGTGC | 11252 |
| rs539381638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958647 | AAGGTCGGACAGACA[C/T]ACTATATACCTTGGG | 11252 |
| rs539400514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913995 | AGACAAAGTCCACAA[C/T]AGATAACGGTACTTC | 11252 |
| rs539431421 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950440 | TGGGCAGGTGGGCAG[A/G]CACAGCATTTTGGTT | 11252 |
| rs539439020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940907 | GTTTTATTAAGATAA[C/T]AATTCACACAGTTCA | 11252 |
| rs539450709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978079 | CAGAGTACAACACTC[A/T]CTCACTGGCTCATTC | 11252 |
| rs539524339 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954195 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 11252 |
| rs539533501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905514 | TCCCTGGCCTGGGCA[C/G]CCCATCACAGAACAG | 11252 |
| rs539582287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972509 | ATCATCAATAAATAC[C/T]AAATATATATATATA | 11252 |
| rs539655031 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936643 | TGGCTGGGCATGGTG[C/G]CTCATGCCTGTAATC | 11252 |
| rs539660586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930636 | ATAACAAAAGGCACG[C/T]TCATAAAAAGCAAAA | 11252 |
| rs539665007 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974623 | GCATGGTGGTGTGTG[A/C]CTGTAATCCCAGCTA | 11252 |
| rs539674495 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923995 | AGCAGTGAGTTACGA[C/T]TGTGCCACTGCACTT | 11252 |
| rs539719354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013296 | CCAAGTAATAAATAT[C/T]ACCAGCCTAATGGCC | 11252 |
| rs539721945 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960594 | TTAGGTGAGGAGAGA[A/C]AGATTTTAAAATGCT | 11252 |
| rs539765682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881126 | CGCAGGGGAGTGCTC[A/G]GCAGCAGGGCCCACA | 11252 |
| rs539784414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961052 | GTGGTAATGGCCAGG[A/G]CAGGGCCAGTTCAGG | 11252 |
| rs539788675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875446 | ACAATCATGATTCAT[C/T]GCAACCTCAATCTAC | 11252 |
| rs539803021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944174 | CTCTCAGAGAGTGCT[A/G]TCTCCTTAATCAGCC | 11252 |
| rs539808112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951043 | CTTGAATGAACATCT[C/T]TGGGTGGTGGAACAT | 11252 |
| rs539834239 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931161 | ACCTGCCTTGTTCAC[A/T]GTTGTATCCCACGGC | 11252 |
| rs539861773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000874 | ATTGACTTTCTTCCC[A/G]TGGCTTACAGGTGGT | 11252 |
| rs539862853 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870198 | CTACTGCAAAGACGC[C/G]GGCACTTTTACAGTG | 11252 |
| rs539866150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944741 | AGCTATTTTCCATCC[A/G]AAATTGGGTATAAGC | 11252 |
| rs539885725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983266 | AGGCTGCAGTGAGTC[A/G]ACAATGTGCCACTGC | 11252 |
| rs539893594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987724 | TTTTAGTAGAGACAG[C/G]GTTTAATCACTGTGT | 11252 |
| rs539897701 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870576 | TCTGAATCAGTGATA[A/C]AATTGTTAATTTGCA | 11252 |
| rs539953277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988292 | GGACCCTCACAGTTA[C/T]AAAGCCCACGAGGAC | 11252 |
| rs539967146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938430 | AGGCGTCAGAAAGAA[A/G]CCTGACCTTCTCCCT | 11252 |
| rs540021554 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942873 | TTCTCTGACTTTTCA[A/C]AACTGTTCTGACTAT | 11252 |
| rs540026281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997746 | TGGTGGCGCATGCCT[C/G]TGGTCCCAGCTATTA | 11252 |
| rs540069631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980361 | TCTACTAAAAATCAA[A/G]AACACTAGCTTGTCA | 11252 |
| rs540126653 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970538 | AAAGGTAGACAGGAA[A/C]TCTATTAGTTTTGCA | 11252 |
| rs540130662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974428 | TCCTGGTCTAAGCCA[C/T]GCCTAACTCCTCCCC | 11252 |
| rs540168453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894890 | TTACCTTTTCTAAAA[C/T]CTCTTTGCCTGGCCC | 11252 |
| rs540190340 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883877 | GGTGTGGTGGCGCAT[G/T]CCTGTAATCCCAGCT | 11252 |
| rs540200058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964534 | CTTTCCCTAGCAGGC[G/T]AAAACTAACAGCTGA | 11252 |
| rs540269455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004425 | TGATGACACATTTGC[A/G]GGAGCAAAGGTCGCA | 11252 |
| rs540270337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990194 | TCTGCAGTCAGTCAA[C/T]GTGACTTTCCACATG | 11252 |
| rs540276611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901637 | ACACTGCACGGTAGG[C/T]TTCTTCCCAGCCAGC | 11252 |
| rs540291112 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882659 | AACTGGAGGGTGTTA[A/G]AAAGTACCCCTCCTT | 11252 |
| rs540293562 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897403 | TGTAATTAAAAACCT[-/C]TCTTCTACTTCTTCA | 11252 |
| rs540306356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958911 | AGAATTACAGCACCA[C/T]AGCAATAAAGGGGAG | 11252 |
| rs540333522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997770 | GCTATTACTTCACTC[A/G]GGAGGCAGAGTGAGG | 11252 |
| rs540336366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975382 | CCAGCACTTTGGGAG[C/G]CTGAGGCAGGAGAAT | 11252 |
| rs540347874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984593 | GGTTGACAACACCTG[A/C]TGCAAAGGTTCCTGG | 11252 |
| rs540353305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895930 | TATCGCCATAAACCA[C/T]CAGGGACAGAGCAAT | 11252 |
| rs540374333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873454 | AGGGGAAGAGTGTCT[A/G]GGGACAGCAGGCTGG | 11252 |
| rs540402951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991663 | GAAAGCCATGCCATA[C/T]GAAGCTGAGAACAGT | 11252 |
| rs540413890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933131 | AACCTAGTCTATTAT[A/T]ATCTTTATGTGTCAG | 11252 |
| rs540417544 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888264 | CCACACCCATTCACA[C/T]CCACCACTGGCCACA | 11252 |
| rs540419794 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952313 | GTTGAAGAAATTTAT[G/T]TATTTATTTATTATT | 11252 |
| rs540426571 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015216 | TTGGCTACCGGACAC[A/C]GAGCCCCGCCCCACA | 11252 |
| rs540462881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992272 | AAAGACTACATGTAC[C/T]AAGTGTTGGTGAGGA | 11252 |
| rs540464617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985403 | AGCCATTCCTGATGG[G/T]CTCCACGTTCTGCCC | 11252 |
| rs540470389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009694 | CCCCTCTGTCATCTC[A/G]TATTCTTGGGAGGAA | 11252 |
| rs540476828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985997 | GAAACATCGAGGTCT[C/T]CTTGATTGGGCCAAT | 11252 |
| rs540509582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897672 | GGACTGCCTGGCAGA[C/T]GGAGGGCCAAGCATG | 11252 |
| rs540516766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903255 | CACCCACCTTCCCTG[A/G]GGAGGGTGTGCGTGT | 11252 |
| rs540521275 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984869 | AGAGGCAACTACTTA[C/T]CTGAAAAAAGCAGCT | 11252 |
| rs540546262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898459 | TATTTTTAGTAGAGA[C/T]GGGTTTTCTGCATGT | 11252 |
| rs540558017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010015 | GCTGAGATTATAGGC[A/G]CACGCCACCATACCC | 11252 |
| rs540594293 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010619 | GGAGGCTGAGGCAGG[A/G]GAATGGCATGAACTC | 11252 |
| rs540595597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880671 | ATTAGAGAAAGGCAT[G/T]GTCCCGTAACAGCTG | 11252 |
| rs540601070 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915177 | CGGGCCTAAGATTTA[A/G]GAGCCCACTAAGTGC | 11252 |
| rs540606752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963304 | CCTACTCAAACCATG[C/T]GGATTAAGGCGGAAG | 11252 |
| rs540610848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921134 | GGAGGCCGAGAAGGG[C/T]AGATCATGAGGTCAG | 11252 |
| rs540621852 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997149 | GGGGTGTTTAATCAC[A/G]CTCTGCCTCCTCTGA | 11252 |
| rs540626511 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924810 | CGCCCAGGCTGAAGC[A/G]CAGTGGCACGATCTC | 11252 |
| rs540629585 | snp | A/G | 1.68533e-05 | 0.00290282 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879204 | GGAGAGAAACCAAAG[A/G]TTCACTACTTGCTGG | 11252 |
| rs540671716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921824 | GCTCACTGCAACCTC[C/T]GTCTCCCGGGTTCAG | 11252 |
| rs540675098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999578 | GGAGGCTGAAGAAGA[C/G]AATCGCTTGAACCCG | 11252 |
| rs540692636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993674 | CGTTGATGATAACAC[G/T]ATTGCAGACTGTCAT | 11252 |
| rs540711129 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911386 | CTGAACTCCAGCCTG[C/T]GCTCTCGAGACCTCA | 11252 |
| rs540719463 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881260 | TGGGCCTGGGTCAAT[A/G]GCCCTGCGTGGACAA | 11252 |
| rs540731881 | in-del | -/GA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919798 | AAAAAAAAAAAAAAA[-/GA]AAGAAAGAAAGAAAA | 11252 |
| rs540741334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999112 | ACTGACTCTTAAGCC[A/G]TTTAACACTTAAGCC | 11252 |
| rs540745525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954166 | TACTTGGGAGGCTGA[A/G]GCAAGAGAATCACTT | 11252 |
| rs540798921 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870029 | ACACAGGTTCCCCCA[A/C]GTTCCCCCCACCCCC | 11252 |
| rs540807745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994033 | GTGGGATTCCTCCAG[A/G]CTAAAGTCCAGTGAG | 11252 |
| rs540869120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987786 | TCATCTACCCACCTC[C/T]GCCTCCCAAAGTGCT | 11252 |
| rs540876296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976933 | AGAAGTTTCTCCAGC[C/T]GACACAATACCTCAT | 11252 |
| rs540880838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949337 | TCTCTGGCAACTCCC[A/G]CCCCACACAGGGAGG | 11252 |
| rs540883078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988523 | TTCAGCAACCTGTAG[A/G]AGTCCAGGCTTAGGG | 11252 |
| rs540919493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979943 | ATTTATTACACATAC[A/G]CACATACATACAATA | 11252 |
| rs540948880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900956 | AGCCAGCCCTGTGGG[C/T]GCCAGCAAGTCACAA | 11252 |
| rs540952485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894094 | TACCATGTGCCAGGC[A/G]ACCTGCTAGGTGTTT | 11252 |
| rs540954104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906179 | TCCCTGTCACACTCA[A/C]CTCTGTGTCCCAGCC | 11252 |
| rs540989519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894531 | CAGGCGTGAGGCACC[A/G]CGCCCAGCCCAAAGG | 11252 |
| rs540994921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936201 | AGCCTGGGCGGCAGA[G/T]CGAGACTCCGTCTCA | 11252 |
| rs541008241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923679 | TGATCCGCCCGCCTC[C/G]GCCTCCCAAAGTGCT | 11252 |
| rs541022722 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996227 | TCCGTCTCAAAAAAA[A/T]AATAATAAAATTAGC | 11252 |
| rs541058543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931163 | CTGCCTTGTTCACAG[C/T]TGTATCCCACGGCTG | 11252 |
| rs541061306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013581 | GGCAAGAACAGGAGG[A/G]CTGGCATTCAACACT | 11252 |
| rs541065887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924220 | AAGGACATGACCAGA[C/T]CCCCTGCATCTCTCC | 11252 |
| rs541067555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917662 | CACGCACTGCTCTGC[A/G]GTGTGCCGTGATGAA | 11252 |
| rs541079934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918063 | TGGTGAGGGTCAACT[A/G]AGAAGGATGTGAAAA | 11252 |
| rs541080387 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986938 | GCCCCTAAGATCCCC[-/T]TCTTGAGTAAAGTTT | 11252 |
| rs541088547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000307 | CAGGGCTTTGCAGCC[C/T]TTGTGGGGACTGGTA | 11252 |
| rs541094936 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946406 | ACATTGGCCTCTGAG[A/C]CTGGCGAGAGCAGCA | 11252 |
| rs541095600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925275 | ACTTGAGGTCAGGAG[C/T]TTAAGACCAGCCTGG | 11252 |
| rs541108909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961313 | TTAGACAAACACTGC[A/G]GAAGGCCGCAGGGTC | 11252 |
| rs541134185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932037 | CTTCCCTTCTCTAAA[C/T]CATCACATCACTTCA | 11252 |
| rs541135829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911563 | CTGGCGGCAGATGCT[C/T]CAGCAAGTTTGAAGG | 11252 |
| rs541149097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014181 | GGCTTGAAAGCCCTA[C/G]AGGAGTAAGGAGTTC | 11252 |
| rs541156404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974644 | ATCCCAGCTACTCGG[A/G]TGGCTGAGGCACCGT | 11252 |
| rs541158277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954882 | AAATAGAATTAAGAA[C/T]AAACTGGTTTGGATC | 11252 |
| rs541165923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948101 | GCAGGAGCAGCAAGG[A/G]AAGGCATCCCAGGTA | 11252 |
| rs541178261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948674 | TTTTAAGTACAAACC[A/G]TGAGAGGATTTGGTT | 11252 |
| rs541187845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008540 | AGGCGTTAGCCACCA[C/T]GCCCGGCCTAAGTTC | 11252 |
| rs541188608 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870301 | TCCAGCAGGCACCAC[A/G]TCAGAGAGGCCCCAG | 11252 |
| rs541202225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889356 | TCAGCCACATTTCCT[C/T]TGGTTTTAATGGTTT | 11252 |
| rs541225537 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988067 | ACTTGAACTCGGGAG[A/G]TGGAGGTTGCTGTGA | 11252 |
| rs541243329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942589 | TAAGTTTTATATGTG[A/G]CATGAGGCAGAGATC | 11252 |
| rs541247725 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870103 | CTCCCGGGCGACTCC[A/G]GGCAGCCCGAGACAC | 11252 |
| rs541256043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001233 | AGGGGAGCTAAGAGC[A/G]TATGGTTCTGGGCTT | 11252 |
| rs541260203 | in-del | -/AC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880609 | GGTAGCCGAACGCAG[-/AC]ACTTACTTCATCCTT | 11252 |
| rs541300519 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964997 | AAGATGGGGAGGGCA[C/T]GCACACACTCCTGTA | 11252 |
| rs541305169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912374 | GTGATGGGGGCGAGG[C/G]GTGCATGTGCATAAA | 11252 |
| rs541327799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002393 | CTCCAAGGATTAATC[A/G]TCAAGTAGTAAGGAT | 11252 |
| rs541332008 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938622 | CCAACTGCATGTTCC[A/G]CAGGACCATTTAGGT | 11252 |
| rs541332777 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982099 | GACCCCTCTGCCCGG[A/C]CAGCCGCCCCGTCCG | 11252 |
| rs541337653 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990724 | AGTCTGGATTTTATT[G/T]TGATAACAACAGAGA | 11252 |
| rs541339099 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017412 | ATGTTGCCCAGGCTC[A/G]TCTTGAACTCCTGGG | 11252 |
| rs541398818 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941318 | CATTTGGGTTGTTTG[A/C]CACTTTTCCGCTATT | 11252 |
| rs541419494 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931545 | CAATGGAACCAGCCA[G/T]GGTTCAGAGGGCTCC | 11252 |
| rs541441650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973910 | GGGGACACATAGCTC[A/G]GGTGTGGATGCCAAG | 11252 |
| rs541457678 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016273 | AGATAGGTATGAGAA[A/G]AGAGTCCACAAAGAA | 11252 |
| rs541463560 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897558 | ATGAAGCTATGTTCC[C/T]AACTTCCTCTAAATT | 11252 |
| rs541524779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968032 | TAACCTTGCAAGGTG[G/T]GAGTACTGCGCCAGT | 11252 |
| rs541546258 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016881 | CTTGTCGGGCGCTGT[A/G]GCTCACGCCTGTAAT | 11252 |
| rs541547528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881964 | TAGAGAGGACATAAC[C/T]GCGACTTCAGGAGAG | 11252 |
| rs541557913 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919199 | AAGAGAGTGTGATAT[G/T]GAGTCGAAAATGAGT | 11252 |
| rs541575140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884757 | TCCTGCCATCTGCCC[C/T]GTCTCTCAGCTGGAG | 11252 |
| rs541600627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921888 | GGATTACAGGCGCTC[A/G]CCACCATGCCAGGCT | 11252 |
| rs541604084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875389 | TTGTTTGTTTGTTTG[C/T]GACAGGGTCTCGCTC | 11252 |
| rs541610278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876816 | TGCCGAGGGGTGAGA[A/C]CCCTGGACAGAGAGA | 11252 |
| rs541615689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001909 | TGTCCCTGCTAAGCA[C/G]CTTGTCCTTTGCAGA | 11252 |
| rs541659990 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922459 | AGCTGGCCTCGGGAG[A/C]AAGCCCCCGATACCC | 11252 |
| rs541664342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913033 | TCACATGAATCTTCA[C/T]GATTCTCTGTGACAC | 11252 |
| rs541711553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916406 | ACAACCTGGGGTGGG[G/T]GTGGGGATGGGGGGT | 11252 |
| rs541718907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907066 | CCCTAGGAAGGAGAT[A/G]GAAGTCTGGATGGAG | 11252 |
| rs541757718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950386 | AAAGATAAGACAAAG[G/T]CATACCAGATTAGGC | 11252 |
| rs541772872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909844 | AGCAGTTTCTGCCAC[C/T]AAGTGGGTAATGAAG | 11252 |
| rs541775230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946880 | GTTGCAGGGAGCTGG[A/G]CCGTGGGTCCGGGTA | 11252 |
| rs541790789 | snp | C/G/T | 0.000662893 | 0.0181938 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871390 | ATAATTTGCCGGGTA[C/G/T]AGGCCAACTTGCCCG | 11252 |
| rs541802645 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933870 | ATGCTGAAGTGTGTG[A/T]AAGTATGAACAAGCA | 11252 |
| rs541834631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940507 | AGGGAGGGGGAAAGA[A/G]GCCCAGTCTCCAAGG | 11252 |
| rs541836688 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947480 | CCATGCTTGGAGGCA[G/T]CCGTTTCAGAGGCTC | 11252 |
| rs541910507 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005117 | AAACTTCCTATAATT[C/T]TAAAGCCTTAACTAT | 11252 |
| rs541931105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010767 | AAAAAGACCTTATTC[C/T]AGGAAACAAGAAAGA | 11252 |
| rs541944093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970974 | CTCCACAGCCCTCTC[C/T]GCTACAGCCTACCCC | 11252 |
| rs541947931 | snp | A/C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949223 | GGTGGCTGACCTACA[A/C/T]AGAGTAGGAATTTAA | 11252 |
| rs541956164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971374 | CTGCAGACGGAGTCT[C/T]GCTCACTCAGTGCTC | 11252 |
| rs541957507 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907576 | GCTGACACAGGCAGG[C/T]CATCACACGGAAAAG | 11252 |
| rs541982281 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959065 | TGTCTAGTGACAGCC[C/T]TCAGAGGGGGACGAG | 11252 |
| rs541999225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879281 | TCTGTGCATCTGATG[C/T]GTAGACTCAGGGCCC | 11252 |
| rs542010529 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965239 | AGCAAAACCAATCTA[C/T]AGTGACAGATTAATG | 11252 |
| rs542019803 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965490 | AAGAAAAGCCCCCAG[A/C]AGAAGTCTAGTAACA | 11252 |
| rs542046734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935121 | CAGTAGAGTCGGGGT[C/T]TCACTGTTTTAGCCA | 11252 |
| rs542047905 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915648 | CACCTTCCAACTTAG[A/G]CATTCTCCGAGATTA | 11252 |
| rs542070821 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874762 | CTAGCCAGTGCCCTG[A/C]AATTCACAGCCTTGG | 11252 |
| rs542073579 | in-del | -/AAAAAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913498 | AAAAAAAAAAAAAAA[-/AAAAAAA]GAGAGACACTAATGG | 11252 |
| rs542083977 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943388 | CTTTTGTTTTCTTGT[C/T]TAACTTCGAAGTTCC | 11252 |
| rs542106417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966301 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAATGAG | 11252 |
| rs542106649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972238 | CTGAAACATGTGCTG[C/T]GTCCACTCAGGGTTA | 11252 |
| rs542111671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998258 | ATTCCTTCAGGGACC[A/G]TGAATATAGGAACCT | 11252 |
| rs542118841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967070 | GTAGGGTAGACGGAC[A/G]AGTACCCAGAGGACC | 11252 |
| rs542118973 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941881 | TCCTGGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC | 11252 |
| rs542122663 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919649 | GTGGTAGCATGCGCC[G/T]GTAATCTCAGCTACT | 11252 |
| rs542136345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873718 | GAGGGCAAGAGAGGG[A/C]AGAATCTGGGTTGCT | 11252 |
| rs542155816 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886154 | CAGCCTGTGCCGACC[A/C]TGCTAGCCCCAAGTC | 11252 |
| rs542171343 | snp | C/T | 0.107341 | 0.205301 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949463 | ATACACACACGCGCG[C/T]GCACGCACACACACA | 11252 |
| rs542173126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874458 | TGGTTTCTGCTCCTA[A/G]CAACACAGATATGTG | 11252 |
| rs542212932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956150 | GTATGAAATTCATAG[C/T]ACCCTTCACATTAAC | 11252 |
| rs542225553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992456 | CCCCAGGGAAGTGGA[A/G]GCAGATGTTGGCCAA | 11252 |
| rs542225642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998826 | AAACCCCAAACCCCA[A/G]AATCCAGGAGCAGAA | 11252 |
| rs542234709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910352 | GTTCAGTGTTGAGAA[C/G]AAGGGCCTGCACTTC | 11252 |
| rs542260106 | snp | C/T | 0.000101173 | 0.00711168 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871322 | GGCTCCTGGGCCCGC[C/T]GCCTCCGTCCCCCCG | 11252 |
| rs542284883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993028 | AAAATTGGCCGGGCA[C/T]GGCAGCATGCACTTA | 11252 |
| rs542292979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903898 | TCCTGAAACCTGTAT[C/T]CTCAAGTACGAAGGT | 11252 |
| rs542304907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988941 | CTGGAGTGCAGTGGC[A/G]CAATCATGGCTCACT | 11252 |
| rs542306912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912775 | ACCACACCTTGCTAG[C/T]GTGATGACCTGTCCG | 11252 |
| rs542329787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904354 | GCACTGCTCACTTGC[C/T]TTCAGCCGAGCACCC | 11252 |
| rs542330070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898635 | GGATGGACCTTGGGG[G/T]CCACATCCCTCACAA | 11252 |
| rs542410421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935450 | TCCAGACTCATGGTC[C/T]TGTCTAGGGTCAGAG | 11252 |
| rs542437255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978890 | TCCTTCAAAACAATT[C/G]TTTCTCCCCTGGCTT | 11252 |
| rs542437269 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990956 | TCAGTTTCCTCATCT[G/T]TAAAATGGACAGCAG | 11252 |
| rs542440153 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017473 | AAGTGCTGGGATTAC[A/G]CGCACGAGCCACTGT | 11252 |
| rs542448893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974761 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 11252 |
| rs542460369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938372 | AAGGGAAGCCCCTGA[C/T]GCAGAAACTGCATAA | 11252 |
| rs542478002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930317 | GTGCTCTCTGCCCCA[A/G]TTCCACAGCCACAAC | 11252 |
| rs542488912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984066 | GCCTCAACCTCCTGG[A/G]CTCAAGCAATCCTCC | 11252 |
| rs542505598 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916556 | CCCTCCCACGGCACG[-/C]CCGCACCAGCCTCAG | 11252 |
| rs542506859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893262 | GTGGACAAAAGCTCA[C/T]GGAGCCTGTGCCTTC | 11252 |
| rs542530522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882724 | CTTGCCAATGCAGAG[C/T]GTGAAGATGACCCGG | 11252 |
| rs542543695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886930 | GGTGGCTGTCAAACA[A/T]GAAAGGCCTCTTCCT | 11252 |
| rs542546720 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932304 | ACCATTTGGGGCATC[C/G]CTTAGAGAATCTAGC | 11252 |
| rs542561440 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888348 | CCATGTTGGCACAAG[C/T]AGCTCCCTGCAGCAA | 11252 |
| rs542562396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012238 | GGCAAGGTGGCAGGC[A/G]CCTGTAATCCCAACT | 11252 |
| rs542566634 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991758 | TAGAAATTTTCCCCC[-/A]AAATTTTGGGGACTT | 11252 |
| rs542567686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883583 | TCAGAACCAAGTCTC[A/C]GAGGGTATGTGCTGT | 11252 |
| rs542571108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890095 | CAACTTCCACCTCCT[C/G]GGTTCAAGTGATTCT | 11252 |
| rs542626989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001845 | GGACCCAGGGGTAAG[C/T]ACTAAGGTCAGCTGG | 11252 |
| rs542669831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906378 | TCTGTTTTCATAAGC[A/G]TCCAAGCATTGCTTA | 11252 |
| rs542699737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009970 | TGCCTCCCGGGTTCT[A/C]GTGATTCTCCTGCCT | 11252 |
| rs542706787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878061 | CATGTCTGAGCTCAC[C/T]GGCCCTCCTCCCTCC | 11252 |
| rs542725662 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014282 | TGCTTGGCCCCAGCC[A/C]TAGGACGTGCTGCGG | 11252 |
| rs542727860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983214 | CTCAGCTACTCAGGA[A/G]GCTGAGGCAAGAGAA | 11252 |
| rs542745140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901613 | AATGGCCCAGGATAG[A/G]AGGGGTTTACACTGC | 11252 |
| rs542769115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914319 | CTCACTAAAACCTCT[A/G]CTTCCCAGGTTCAAG | 11252 |
| rs542792803 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996934 | AGGAAAAATAGGACA[A/C]CTGGCACAAAATGAG | 11252 |
| rs542799667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937925 | TTCAATCTCCCACTG[A/G]AGAACTCTGGAATGA | 11252 |
| rs542801885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958090 | ATGAACGGACTCATC[A/C]GTAGAAAAAAAAAAC | 11252 |
| rs542820529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872619 | CCCCGGACTGCCTGG[A/G]CTCAAATCCCACAGC | 11252 |
| rs542845402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932267 | CTTCCCTGAGACAAG[C/T]GTATGGCCGGCTCCC | 11252 |
| rs542849310 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959348 | GGGAAAAGCCCTCTA[G/T]TAACAGCTAACTCAA | 11252 |
| rs542855954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990993 | CACAACGCTGTTGTG[A/C]GGACTCAACGGGTTC | 11252 |
| rs542885161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889640 | GCGGAGGAAGGCAGC[A/G]CAAGGCCAGAGAACA | 11252 |
| rs542906745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926065 | AAGCTGGGATGTTTT[C/T]TAAGAGCTCAACTAC | 11252 |
| rs542913676 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903169 | GCCAACCCACGTCCC[A/C]GGCAGCTAGAGGGGG | 11252 |
| rs542955016 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915900 | ATATCCGAAGCCCTA[A/C]GGCGACACTGAGGCA | 11252 |
| rs542962028 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015042 | ATCCGTCGCACACTC[C/G]GTTCAGGCTGCCACG | 11252 |
| rs542965193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009569 | GTCCTTCATTTTACA[A/C]ATATGAAAACTGAGA | 11252 |
| rs542969466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006683 | AGCCCGGCATGATGG[C/T]GCATGCCTATAATCC | 11252 |
| rs543003919 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984770 | TCTTAACACAAGGAG[G/T]GCAGAAAACATCCCC | 11252 |
| rs543021868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005894 | TTGATGGCATTAGGA[A/G]GTAGGGCCTTTGGAA | 11252 |
| rs543033689 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957115 | CTCTAGGATAATGTC[A/G]CCTGGCTCACCAAAT | 11252 |
| rs543040650 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008329 | AATCTCGGCTCACTG[C/T]AACCTCCGCCTCCTG | 11252 |
| rs543053622 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880573 | CCACAGACACCCTGC[A/G]TGGCGTATGGCACTC | 11252 |
| rs543059189 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913885 | GTTAAGTAAATCAGG[A/C]TTCCTACAACCTAAA | 11252 |
| rs543065814 | in-del | -/C | 0.486803 | 0.0811909 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871330 | GCCCGCCGCCTCCGT[-/C]CCCCCCGCTGGCCTG | 11252 |
| rs543074179 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980358 | GTCTCTACTAAAAAT[A/C]AAAAACACTAGCTTG | 11252 |
| rs543083114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999056 | CTGATTCTTCCTGGA[C/T]GCCAGATAATTCGGG | 11252 |
| rs543085010 | snp | A/C | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006643 | AACATGGTAAAACCC[A/C]ATCTCTACCAAAAAT | 11252 |
| rs543093604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957119 | AGGATAATGTCGCCT[G/T]GCTCACCAAATGAAA | 11252 |
| rs543136666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872174 | AGAAGAGGAGATACA[A/G]AGATGAGAGGAACTG | 11252 |
| rs543139986 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880601 | CTCTATGAGGTAGCC[A/G]AACGCAGACACTTAC | 11252 |
| rs543178254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874995 | AGCTGGGACTACAGG[C/T]GGCTGCCACCACGCC | 11252 |
| rs543197549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999393 | TCTGTCTACAGGCCA[C/G]GCGTGGTGGCTCATG | 11252 |
| rs543199605 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910454 | GGCCACAGCCTCTCT[G/T]GGGGGGCCAGCCAGC | 11252 |
| rs543231424 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891697 | AGGCGTGAGCCACCG[C/T]GCCCGGCCATGCCTT | 11252 |
| rs543257400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945468 | CCGCATCTCTGCCTA[C/T]TGGATGCCTCCACTT | 11252 |
| rs543276906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905006 | TGTTACTGAATAGAA[A/G]GGAAAAATGTGTCTC | 11252 |
| rs543296663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993630 | CTAACCTTACACACA[G/T]GAAAACTGCATTGCC | 11252 |
| rs543332242 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939014 | GCATTCAGACCGCTT[C/G]CTCCAGCTGACAACC | 11252 |
| rs543354120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899754 | CCTCTCCCTGGGGAA[A/T]GCACAGGTAAGCACG | 11252 |
| rs543374068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905785 | CAGTGCTCCTGGTGG[A/G]TGGATGGGTAAAAGG | 11252 |
| rs543380617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942006 | GGTCTCGAACTCTTG[A/G]CCTCAGGTGATCTGC | 11252 |
| rs543393867 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016835 | AAGTTCCGCTTACAT[C/T]GCAATTCCATGCCCT | 11252 |
| rs543444057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935796 | CAGCATGAGACCTGG[A/G]GAGCTCAGAGAGTCC | 11252 |
| rs543447372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012169 | AATACATACATACAT[A/C]CATACATACATACAT | 11252 |
| rs543477074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931093 | ATGCCTATTCCAGAC[A/G]CCTGCCTGCTCAAAC | 11252 |
| rs543549012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960666 | CAGCACAAGAAAAGG[C/T]GTAACTAATCTACAC | 11252 |
| rs543556458 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993511 | ATCCTTTAGAAACTA[C/T]CAGCTCTTTTCATCA | 11252 |
| rs543563853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967617 | AAATGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 11252 |
| rs543572003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012885 | TCTCGAACTCCCGAC[C/T]TCTGGTGATCCGCCC | 11252 |
| rs543597372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954089 | AACATAGTGAAACCC[C/T]GTCTCTACCAAAAAA | 11252 |
| rs543604122 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869936 | CACAGGTCCACTTTC[C/T]AAGCAAGACATCTGC | 11252 |
| rs543606062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931499 | AGAGACCTTAGGTGA[C/T]GGGAAGGTAGTGGAG | 11252 |
| rs543619616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925238 | TAATCCCAGCACTTT[A/G]GGCGGCCGAGGCTGG | 11252 |
| rs543622974 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918431 | ACCAGCTACTCAGTA[C/T]CTCTCAGCACCAACA | 11252 |
| rs543626802 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961493 | TAGAAATTCCTTAGG[C/G]TGGGCCGGTGGCTCA | 11252 |
| rs543645814 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011504 | AAGAAACTTTTCGAT[C/G]TGTTTGATATTCCAC | 11252 |
| rs543694142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918322 | ATATTGCCTGGAGTC[C/T]GCCATGTTTGCATCA | 11252 |
| rs543774173 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985426 | TTCTGCCCACAAGGG[C/G]AGCAGATGGGCACAC | 11252 |
| rs543820395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945364 | GCGCTCCCCAGGTTC[A/T]GTCCCAGGCCCTCTC | 11252 |
| rs543838856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900349 | AGTGATTTTCACTAG[C/T]GACGGCGTCATAATA | 11252 |
| rs543875163 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894023 | TGTCATCCATCATGT[G/T]CTGGGTTATTACTTC | 11252 |
| rs543884627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938871 | AAGGTAAAAATGCTG[C/T]CTGTGACAAATTTGT | 11252 |
| rs543895842 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988501 | TGAACTGAAAATCTG[G/T]TTCAAATTCAGCAAC | 11252 |
| rs543905055 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940733 | ATCCCGGAAGTCACA[A/G]TTTAGGAGGCTCAAA | 11252 |
| rs543951539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896627 | GGGGACATAAGCTTC[A/C]ATGACTCTTCGGTGA | 11252 |
| rs543989526 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881425 | AATCTGAATGCAGCC[C/T]GGGCTCTGGCCGCTG | 11252 |
| rs543996342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934293 | CAAATACCAGTCAAT[C/T]TGGTAAAGAGCTACA | 11252 |
| rs544000502 | snp | A/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927450 | GACAGGGTTTCGCCA[A/T]GTTGGCCAGGCTGGT | 11252 |
| rs544002942 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967960 | TATTTTATGACATTT[G/T]ATACACGCTCCTCAG | 11252 |
| rs544015098 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885518 | CCTTCTGAGGAAGGA[C/T]GGAGCGCTTCCCGAG | 11252 |
| rs544030645 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016229 | GCTAGATACAAAATG[G/T]TAGAAACTGTAGAAT | 11252 |
| rs544047091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970908 | CACCCACAGCTGTGC[A/G]GTCAGACAGCGACCC | 11252 |
| rs544063824 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933237 | CATATACCTCCCCAA[C/T]TTTCCTTAAATCCTG | 11252 |
| rs544068238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919063 | CGTATGGGACAAGCT[A/G]CTCTTTAATGCCAAA | 11252 |
| rs544101702 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977142 | TAATTTCATTTAGAC[C/T]ATGGATGGAAGAAGA | 11252 |
| rs544111516 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983988 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTGGC | 11252 |
| rs544116704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881880 | GTCCTGTGTGCCTAC[A/G]GCTCCTGAGACTGAC | 11252 |
| rs544136207 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921193 | TGAAACCCTGTCTCT[A/G]CTAAAAATACAAAAA | 11252 |
| rs544153058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921864 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 11252 |
| rs544161328 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964663 | TTCCTATGTACCTGG[G/T]TCCCTGAACTTTGCA | 11252 |
| rs544207430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879246 | GTCCTCAGTTCCTGC[A/C]CAGCGAGCCTGCAGT | 11252 |
| rs544250480 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003191 | TTGTGCGTGGAAGGT[A/T]AACTACAAAGAGTTT | 11252 |
| rs544260167 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984676 | CAGGGTAAACCAGAA[A/G]GAAAGGAAAATGAAA | 11252 |
| rs544281120 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952722 | GGCTGGAGTGCAGTG[A/G]AGCGATCTCGGCTCA | 11252 |
| rs544307832 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878327 | CTGGGGAGCCTGGGT[-/G]GGGGCTTCAGTGCCT | 11252 |
| rs544321031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976320 | CTATAGAGCAAGGCC[A/G]GAAGCTACACCCTGG | 11252 |
| rs544341139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992343 | GCACTTTGGAAAAGT[C/T]TGGCAGTGTCTGGAC | 11252 |
| rs544375170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883953 | AGGAGGTTGCAGTGA[A/G]CTGAGATCACGCCAC | 11252 |
| rs544424979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946764 | GAGGACGCGTCAGCT[C/T]ATCTCTGCCACCACT | 11252 |
| rs544475601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887373 | CCTGCTGGATGGCAC[A/G]TGACTTAACCTCTCT | 11252 |
| rs544483426 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903452 | CCAAAGAGTAACAGG[-/T]GGTCCTTGAAAAACC | 11252 |
| rs544484985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878886 | CCACAGAGCTCAGGA[A/G]CCCAGGAACCTCCCA | 11252 |
| rs544491164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004469 | AGCATCACCACGTGC[A/G]AGCTAAGTGGCGAGC | 11252 |
| rs544498094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978177 | GAGCTTAAATTCAGG[G/T]GTGTGTAAGCTCAAG | 11252 |
| rs544510234 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971914 | CCTCCACCCGGCCGC[C/T]GCCCCGTCTGGAAGG | 11252 |
| rs544522437 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885398 | GGGGTGGGTGAGAGA[C/G/T]AGCAGGGCTGGGGCC | 11252 |
| rs544531095 | snp | A/G | | | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879161 | TCGATTCAGGTCTGC[A/G]GACCACTCCTAGGCA | 11252 |
| rs544562822 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891686 | GCAGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 11252 |
| rs544575649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955039 | TACCTGACAAACCAC[G/T]CCCTCTAAAACTCAT | 11252 |
| rs544599906 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997805 | AGAATCATCTGAACC[C/T]GTGAGGTGGAGGATG | 11252 |
| rs544601338 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986705 | CTGAGAGGGGGCTTT[C/T]GTGCTATGACCTGAA | 11252 |
| rs544611489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946278 | ATGGGTACCCCAAAC[C/T]TGCCACAGTCTAAGG | 11252 |
| rs544614616 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870437 | ATCTCATTAAAACAG[C/T]AGACGAGTGCTTTAG | 11252 |
| rs544617194 | in-del | -/ACAGTTGT | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938012 | CCCTGCCCTCTACCC[-/ACAGTTGT]ACAGAGTAAAACAAA | 11252 |
| rs544624725 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888225 | TGGTGATTTGGTCCT[C/T]ATAACCCTCCATACC | 11252 |
| rs544638237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991707 | GAGATCCAAGGGCTC[A/G]GAACCACAATTCCCA | 11252 |
| rs544640150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916311 | GGACCTGGGGGACAA[G/T]AATCTGCACCACAAA | 11252 |
| rs544666009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000468 | GGATTGGAGGAGGTT[C/T]CTCTCTCTACTCACC | 11252 |
| rs544677223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909748 | GCTGACAATATACAC[A/T]GGCAACGTTCACCTG | 11252 |
| rs544688024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955521 | CAAGTACAGTTTACA[C/T]AGCCTCACATCATGA | 11252 |
| rs544690566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876702 | TGTGCCCTCCCCGAG[A/G]AATGGGGGTGCCAGA | 11252 |
| rs544722248 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903826 | CGGGGCCTCAATTCT[C/G]TCTCAACTTGGGGTT | 11252 |
| rs544723410 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919009 | ATTCATTCTTCCAGG[C/T]TGAGCCGACTACAAC | 11252 |
| rs544745453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905725 | AATGACAGATTCGAC[A/G]GCCTGCAGCAGCCAG | 11252 |
| rs544747756 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890401 | CCAATGTATGGTTCT[C/G]ATCCTCAGTTACCAA | 11252 |
| rs544759933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955843 | GTGATCAGTCTACTA[C/T]GCCCTGTGCTATTTT | 11252 |
| rs544761619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948732 | CTCAACTATGGTGCC[A/G]CTTTCTCAAGAAAAT | 11252 |
| rs544769519 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902100 | GAGGCCCTAGGGATA[C/T]AGTGGTGAACAAACT | 11252 |
| rs544797981 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927883 | TGAGCCACCGTGCCC[A/G]GCCTCAGTCATTTTT | 11252 |
| rs544811542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941049 | CCAGTCATCCCCCAC[C/T]TCCTCTACTCCCAAT | 11252 |
| rs544821346 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017018 | GCCAGGCGTGGTGGC[A/G]GTCGCCTGTGGTCCC | 11252 |
| rs544837420 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982240 | CCAGCCGCCCCGTCC[A/G]GGAGGGTGGTGGGGG | 11252 |
| rs544840483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934760 | CAACCAAGTTGTTAA[C/T]CCTGGTAGATCAGAC | 11252 |
| rs544855964 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983087 | TTTGGGAAGCTGAGG[C/T]GGGTGGATTACCTGA | 11252 |
| rs544859368 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933639 | GAAGTGGCTCCACAC[A/G]GATGACATAGGTCCA | 11252 |
| rs544915383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989575 | GCCGAGGCGGGTGGA[C/T]CACGAGGTCACGAGT | 11252 |
| rs544954086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935077 | CCCGCCACCGCGCCC[A/G]GCTAATTTTTTTTTT | 11252 |
| rs544955864 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928977 | CAAGCTCTTAGAGTT[A/C]TCTGAGTTTAAAATG | 11252 |
| rs544961339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889513 | TCATTATGAATGGGG[A/C]CAGGGACAAAACAGA | 11252 |
| rs544964917 | snp | A/G | 4.97038e-05 | 0.00498492 | missense | PACSIN2 | GRCh38.p7 | 22:42876205 | CGGACTCGCACTTCC[A/G]TCCCCGAGGTGGCGT | 11252 |
| rs544970764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974001 | ACGAGCTGTGGAATC[C/G]CAATTCAATTTACCT | 11252 |
| rs544984509 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007875 | CACCCTGCCTGTTGC[C/G/T]TTCCACCCACAGATG | 11252 |
| rs545048489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994437 | AAGACCCTCGGGCGT[A/G]CTTATGGGGACACCC | 11252 |
| rs545066419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911627 | CAGCATGATGTCAAA[A/T]CACAGCCCTCCTTGT | 11252 |
| rs545071051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001997 | TAAGGGACAGTGGAG[A/G]GTAGGAAAGTCAGTC | 11252 |
| rs545073837 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001042 | CCCCGTCCGACCTCA[A/T]ATAAAACTTAGGCCA | 11252 |
| rs545111134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988744 | ATCTAATTCATGTTG[A/G]CCCCAGCCCACACAT | 11252 |
| rs545134021 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883408 | TGTGTCTCCTATTAA[C/T]AGCAAGCCTTGACCC | 11252 |
| rs545145393 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956955 | TATACACTAAGAAAA[A/G]GAAGCCGATTGGAAT | 11252 |
| rs545160188 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929558 | GCAAAAGAATGAGTA[C/T]CTCAGAACTCCAAAA | 11252 |
| rs545163692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969603 | GATTATCGCTGTAGA[C/T]TGGAAATAGTTTTCC | 11252 |
| rs545178118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963433 | AGCACTTCCCAGGGG[A/G]ATTCTTTCGCCCAGC | 11252 |
| rs545181242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913181 | TCGCTTGCCTTATCT[A/G]GAAAAAAGAGACAAT | 11252 |
| rs545231596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901168 | CCGCTCCCTCTGCAC[C/T]CTGGAGAGGAAGGGT | 11252 |
| rs545242502 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913717 | CATTACTTCTGTCTC[C/T]ATTTTAAAGTCAAGA | 11252 |
| rs545243743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878005 | TTCAGCCTGGCAAGT[A/G]GTACTTGACCTAGGC | 11252 |
| rs545263115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907712 | CAGGGCACTGCTCTG[C/T]CGCCTCCTAACTGCT | 11252 |
| rs545314574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907995 | CGCCTTCCTGGCAGG[C/G]AACGGTAAATGTTGA | 11252 |
| rs545332722 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935289 | ATATTCCTGATTATC[A/G]AGGACCTGCCTCCTC | 11252 |
| rs545392747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925909 | AGCCTTGGCTCAGCT[C/T]GGGCTATTCATGTAT | 11252 |
| rs545415156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968751 | GGCAAATGTGTCTAT[C/T]AATGTCCTGGAGCTG | 11252 |
| rs545428618 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016924 | GGAGGCCGAGACGGG[C/T]GGATCACGAGGTCAG | 11252 |
| rs545466984 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005252 | TCATTACCAGTACTC[A/C]CTTCCAATCCTGAGT | 11252 |
| rs545472232 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952044 | GAAAGCCTTCCCCCA[A/G]CCCTGATACTCCAGC | 11252 |
| rs545490137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928937 | TCCAACTACTTTCAC[A/G]TGAAAAGAAGAGAGT | 11252 |
| rs545512188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971465 | AGCCGCCTGCCTTGG[C/T]CTCCCAAAGTGCCAA | 11252 |
| rs545518848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011803 | GATCACCTGAGGTCA[G/T]GAGTTCCAGATCAGC | 11252 |
| rs545520066 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877424 | GACAGTGTGGGAGGG[G/T]CCGGCTCCCATGGAT | 11252 |
| rs545551311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922564 | GCTGGGTTCTGGCCG[C/T]TCCACAGGCCTTGCA | 11252 |
| rs545575543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885259 | GGTGGGGATGTGCCT[C/T]GAGGTCAATGACCTC | 11252 |
| rs545590757 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999012 | ACTCAATAAAATCCC[C/G]CATTCACCATCCTTC | 11252 |
| rs545599108 | in-del | -/TCAGGGGGAGGG | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906573 | AATGTCCACTATAGC[-/TCAGGGGGAGGG]TCACCCACCAAAGAA | 11252 |
| rs545623628 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996759 | CACTGAATTTTTTGT[C/T]GGTATTTCTGATGGT | 11252 |
| rs545630534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996089 | GCTGGGCGTGGTGGT[C/G]GGCGCCTGTAGTCCC | 11252 |
| rs545687602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902017 | ATCACTCCATTTCTG[A/G]GCGTCTGGCAACACT | 11252 |
| rs545701568 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876407 | CCCGCCCCGCAAGGG[A/G]AGGGCACTGGAGCCT | 11252 |
| rs545751652 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973655 | CCCACACTTGTGCCA[C/T]GCATGGCCCCCTGCC | 11252 |
| rs545754041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941395 | ATGTTTTCATTTCTT[C/T]TGAGTAGATACCTAG | 11252 |
| rs545762594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951530 | CTCACGGGCCTCTCC[A/G]ACACACTGGCCAAAA | 11252 |
| rs545763844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953413 | AGGAATAAAAAATTA[C/T]ATGTCTATGCAAATT | 11252 |
| rs545770565 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899413 | CTGCCTCGGCCTCCC[A/G]AGTAGCTGGGATGAC | 11252 |
| rs545817941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941893 | GCGATTCTCCTGCCT[C/T]AGCCTCCTGAGTAGC | 11252 |
| rs545827051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947578 | AATATGAGAGACAGC[A/C]AGAGGGGACAACACC | 11252 |
| rs545874406 | in-del | -/AAAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012145 | CGAGACTCTGTCTCA[-/AAAT]AAATAAATACATACA | 11252 |
| rs545875794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971837 | CCAGCAGCCCCGTCC[A/G]GGAGGGAGGTGGGGG | 11252 |
| rs545892378 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923671 | TGACCTCGTGATCCG[-/C]CCGCCTCGGCCTCCC | 11252 |
| rs545907207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965636 | CCAAGTGTATTTCTT[C/G]GGCCTCAATTCTTGG | 11252 |
| rs545917786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959618 | GCATTCTGCATTGCT[C/T]AGTTAATAATGAACT | 11252 |
| rs545923071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899171 | CCATTGCTTTCCACA[A/G]GGTCTACCGCACAGC | 11252 |
| rs545928575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935665 | CCAAATACTGGCTTC[A/G]AGGAAAAAGTGTTTC | 11252 |
| rs545934415 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901837 | TCAGACATTCGACTC[-/T]TGGTTCCATGGGCTT | 11252 |
| rs545958768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923126 | ATCATAGATAAGCTG[C/T]ATGGTAACTCAGAGT | 11252 |
| rs545985293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960129 | CCCCCTCCCCAACAC[A/G]CAAAAAATCAAATTA | 11252 |
| rs545985906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936085 | GCCGAACATGGTGGC[G/T]GGTGCCTGTAGTCCC | 11252 |
| rs545995173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874526 | GGTGTGCACACACAC[A/C]AGTTGCTGCCTGAGA | 11252 |
| rs545996920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972359 | CAGTACCCAGGGACA[G/T]AAACATTGCGGAAGG | 11252 |
| rs545997399 | in-del | -/A/AA | 0.495596 | 0.0467178 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936215 | GCGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 11252 |
| rs546028111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874944 | CAAGCTCCGCCTCCC[A/G]GGTTCAAGCAATTTT | 11252 |
| rs546050781 | in-del | -/AC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949666 | CCCAATACCCCCACT[-/AC]ACACACACATACACT | 11252 |
| rs546070855 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969260 | GTATCTCATTTTACA[A/C]ATTTCTTTTCAACAA | 11252 |
| rs546087225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923807 | TTTGAGAAGCTGAGG[C/T]GGGAGGTCTGCTTGA | 11252 |
| rs546092233 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921959 | GGCCAGGCTGGTCTC[G/T]AACTCCTGAACTCAG | 11252 |
| rs546092477 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961383 | ATCTGTTGACCTTCC[C/T]TCCACTATTGTCCTA | 11252 |
| rs546111659 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967160 | GGGACAGGGGGCCAG[G/T]AAGAGATGTGAGAAG | 11252 |
| rs546126530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953916 | GGAAGAGAGGAATGC[C/T]TAGAGCAAGAATGGT | 11252 |
| rs546149908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937235 | GACCAGAGAAGGTCC[C/T]CAAAGAAGGTGACAC | 11252 |
| rs546157079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993566 | AATGTAAAAGATACA[A/G]TGGTCAAAATTTTAT | 11252 |
| rs546179051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880730 | GCTGGTTCCCAGCCC[A/G]TGGACCCACAGAGAG | 11252 |
| rs546260889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899702 | GGGCTTAGATTCCCA[C/T]AGAAGTGTTCCCTTT | 11252 |
| rs546306601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968884 | CTGGACTGAGAGCTA[C/T]ATGACTGGCTTCTCT | 11252 |
| rs546333829 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919616 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 11252 |
| rs546337487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979598 | AAATATAAAAACAGT[C/T]AAAAAACAAAGAAAG | 11252 |
| rs546351529 | snp | A/G | 1.65603e-05 | 0.00287747 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876975 | CTGGACTGTGACTGC[A/G]CAGACTGGGCGGGGT | 11252 |
| rs546370601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012382 | CCTGGCCATCAGAGA[C/T]GTGGATGGGTATCCA | 11252 |
| rs546376366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893806 | TATTATTAATAAGAT[C/T]ATACACATCAGTGAA | 11252 |
| rs546385881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931050 | GGAATTCTTTCATTC[A/C]CTCATTCATTCGCTC | 11252 |
| rs546397890 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937785 | CACCCATGCAGCTCC[A/G]AGAACAGCAAAGTCC | 11252 |
| rs546404223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967626 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11252 |
| rs546440336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882772 | ACCAAGACGGGGTGG[A/G]GGCTGCCTTCCGCCT | 11252 |
| rs546467397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967587 | GCATTGTGAGTTGGT[A/G]TTTAGAAACCCTGCA | 11252 |
| rs546480034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963601 | CGTTTACCACGCTCA[A/T]TTGAAACACTATAAG | 11252 |
| rs546486922 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876079 | AAAACAAAAAAGACC[-/G]CCCACAGCCTGCAGG | 11252 |
| rs546488556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877645 | CCTACTGTTTGCCAG[A/G]CCCAGTGTGGGAACC | 11252 |
| rs546512483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881367 | AGTCACAAAAAGGGC[A/G]AATAGTTTGCTCAGC | 11252 |
| rs546515252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887603 | GGCAGGGCAGGCCCT[A/C]GGCAATCACACCCCC | 11252 |
| rs546525319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871720 | GCTCTCAGCTGCCAC[A/G]GTGGCTCCCACTGAG | 11252 |
| rs546555472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982882 | AATAAAAAAAAAAAA[A/C]AAAAAAAACAACAAC | 11252 |
| rs546560027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872232 | TAGGGTGGTGAGGGG[A/G]AGGTGGCACTAGGGT | 11252 |
| rs546574394 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990007 | ACATATATACACACA[C/T]ATATATATACACACA | 11252 |
| rs546581280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957326 | TGAAAGTGCCAGTTT[G/T]CCTGAAGTGCTTTTG | 11252 |
| rs546590761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990589 | TTGAAGGATGAGTTC[A/G]GCAGGCAAAGACGGG | 11252 |
| rs546605392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878218 | CCACCCCCAAGCATA[C/T]AGGTGCTGGCCTGAT | 11252 |
| rs546644173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013951 | CCCTCAGGCACCCAA[G/T]CCAAGAGTGGCATCC | 11252 |
| rs546654077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984271 | GCTACCACCCACTAC[C/T]TAGCACTTAGCACTT | 11252 |
| rs546654163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991087 | GTGCTAGGACTAGTA[A/G]TACCAGCAGTTTATG | 11252 |
| rs546657625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889133 | ATTAAGTGTAGGGGA[C/G]GACAACTGAGACGGA | 11252 |
| rs546662688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894876 | ACCCCTTGTCAGTTT[C/T]ACCTTTTCTAAAATC | 11252 |
| rs546701290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895503 | TTGAAACCTGCTTAT[C/T]TCTGTGATTTTCAGA | 11252 |
| rs546708748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925625 | ACAAGAAAAGTTGAA[C/G]AGCCTGGGTAATTTT | 11252 |
| rs546709998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907778 | GGGCTCTCATATGGG[G/T]TGCCCAGGACTTAGC | 11252 |
| rs546767907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984908 | GTTGGAAAACAAAAG[C/T]AGGCCCCACCCCTAG | 11252 |
| rs546768257 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008871 | TGCTAAGCAACTGAG[A/T]AGTAGTCATTTTAAT | 11252 |
| rs546811394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919577 | CAGGAGTTTAAGACC[A/C]GCCTGGCCAACATGG | 11252 |
| rs546846710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995615 | CAATGTCATTCACGC[A/G]GCAATTATTTGGAAA | 11252 |
| rs546881444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950687 | AGCTGAACACTTGGG[A/C]TTTATCTAAAAATAT | 11252 |
| rs546902222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933964 | TGTTTAAAAATAAAC[C/T]GGATACTCAAATACC | 11252 |
| rs546903018 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010447 | AGGCACGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 11252 |
| rs546906227 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015911 | TGAGCCAGGTAACTT[G/T]CTGGGGGTGATGTGG | 11252 |
| rs546918900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976368 | GCGCAGGCCTTAATG[C/T]ACACTTGCTCCAGAC | 11252 |
| rs546923289 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989634 | ACCCCGTCTCTACTA[A/T]AAATACAAAAAAAAT | 11252 |
| rs546930961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970592 | TTGTAAAATAAAAAG[C/T]TTATTATAGAAATAA | 11252 |
| rs546967009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907392 | ATGGTTCAGCAGATA[A/C]TAGTTCAGTGAAAAG | 11252 |
| rs546990622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993123 | AGGTTGCAGTGAGTC[A/G]AGATTGCACCACTGC | 11252 |
| rs547026561 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935096 | AATTTTTTTTTTTTT[A/T]TTTTATTTTCAGTAG | 11252 |
| rs547052493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986674 | ACTTCAGGGCAGAGA[A/G]CAACATCAGTGACCA | 11252 |
| rs547057508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910072 | AGGCAAAGAAAAATC[A/G]GTAACTTGCCCAAAG | 11252 |
| rs547086417 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960179 | ATACATGAGTCTTCT[-/A]AATATCTTCTTGTAT | 11252 |
| rs547101544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945092 | GACAGGGCAAGACTC[A/G]TCTCAAAAAAAAAAA | 11252 |
| rs547113829 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918016 | ATAATGTTTACTGCA[A/C]CAATATTATCCCCAC | 11252 |
| rs547151619 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922145 | CAGCAATGTATGTAA[A/G]TACAGTGAGTCAGAG | 11252 |
| rs547163516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885011 | CTTCACAGTGTTCTG[A/G]TATGTACATGATGGG | 11252 |
| rs547164846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938621 | GCCAACTGCATGTTC[C/T]GCAGGACCATTTAGG | 11252 |
| rs547190915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926958 | CAGCTCTGAAGCTCA[C/T]GATTCCTGTTCAGGA | 11252 |
| rs547232037 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015360 | GGAGTGCCTATTTAA[C/T]GGGCTGCGAGGGTGG | 11252 |
| rs547235868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935338 | GACCTAACTCACCAT[G/T]TCTCTCCTTTTCCCA | 11252 |
| rs547237150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899851 | ACAGAATGATGTGGG[A/G]CATGATGCCATTTAC | 11252 |
| rs547245342 | in-del | -/AGCGAGACCTGG | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924026 | CAATCTGGGTGACAA[-/AGCGAGACCTGG]TCTCTTTAAAAAAAA | 11252 |
| rs547280326 | in-del | -/CT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949705 | ACACACTCACACACA[-/CT]CTCTCACACACACAC | 11252 |
| rs547290313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971054 | CTAAGCTAAAAACAA[C/T]GAAAGGAGGTGGCAT | 11252 |
| rs547294942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930057 | TGTGTCCCAATCCTA[C/G]CACAAAGTTCGCCGT | 11252 |
| rs547297062 | in-del | -/GAGAGGAAGTC | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998859 | TGGCAGAGGAGAGAA[-/GAGAGGAAGTC]GAGAGGAAGTCGAGA | 11252 |
| rs547301045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012533 | TCACCCAGGCTAGAG[G/T]GCAGTGGTGTGATCT | 11252 |
| rs547318238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972066 | GTTTTGTCCAATGGG[G/T]GGGGGAAATGTGGGG | 11252 |
| rs547335534 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964361 | AGGTGGAGGTTGCAG[A/T]GAGCCAAGATCGTGC | 11252 |
| rs547343525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953645 | GGTTTCATTTAACAC[A/G]AGGAAAAAACCATTG | 11252 |
| rs547355795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886508 | TCTCACTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 11252 |
| rs547377453 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869348 | CTCTGTTTCCTCCTC[A/G]GTAGAATGGAAATGG | 11252 |
| rs547379146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923915 | GGTGTGGTAGTGCAC[A/G]CCTGTACTCCCAGCT | 11252 |
| rs547393226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917891 | CAGCCTCCCAAGTAG[C/T]TAGGACTACAGAGTG | 11252 |
| rs547396308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917097 | CCCCATGCACTACAC[A/G]CGTGCACTCCATTTA | 11252 |
| rs547401203 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968319 | AATAACCAACTCAAA[C/T]CCTTAGTGAAACCAG | 11252 |
| rs547454198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918545 | AAGGCAACCAAGATA[C/T]AGATAATTCAAATCA | 11252 |
| rs547502040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947681 | CCCTGGGGGTGGGGG[A/G]GGGGACCTCTTAATG | 11252 |
| rs547563558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941615 | ATATCTCATTGTGAT[G/T]TTGATTCGTGTTTCC | 11252 |
| rs547570468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881486 | CACAGCAGAGGTAGT[C/T]GCCCTCAGCATCCCT | 11252 |
| rs547572770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954498 | CCTCCTGGGTGTAAG[C/T]GATCCTCCCACTTGA | 11252 |
| rs547584468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935883 | ACTGGCCACGTTACC[C/T]AGGTACATTCTATCA | 11252 |
| rs547607538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979204 | GGTTCATCTGTTTGT[C/G]TTTTTATTTATAGAT | 11252 |
| rs547669038 | in-del | -/TGCTTCTATTT | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907245 | CCATGCTAAAGAGTA[-/TGCTTCTATTT]TGAAGGTGATGCAGA | 11252 |
| rs547671029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942765 | TCTATCTCATTTTTC[C/T]ATGTCTATCCTTATG | 11252 |
| rs547698402 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930605 | ATTTGGAAGTATGAA[A/T]GTAGGTCATTTTGAA | 11252 |
| rs547724930 | snp | A/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896806 | TGTTCTGTTTTGTTA[A/T]TTTTAGCCATTCTAC | 11252 |
| rs547726369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880922 | GTGTCTGAAACCCCA[C/G]CTGTGCACAAAACAC | 11252 |
| rs547729428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967210 | TCTGAGCTGAATCAC[A/G]TAAACAAGGGCCGTG | 11252 |
| rs547730353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943440 | TATTGAGCAGAAGGA[C/G]TGAGAACAGACATCA | 11252 |
| rs547732295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936615 | TATCAAAGCAGAAAT[A/C]AAGATGGGGTTATGG | 11252 |
| rs547735686 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991834 | AAAAAAAAAAAACCT[G/T]CAATTCACACACCGC | 11252 |
| rs547783324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007520 | CTCTCCCAGCCACTC[C/T]TTGTTCTTCAGAGCT | 11252 |
| rs547784059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927499 | AGTGATCCACCCATC[C/T]TGGCCTCCCAAAGTG | 11252 |
| rs547798024 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889204 | CACGCACATGGAGCA[C/T]GCACATGGAACACGC | 11252 |
| rs547839871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967660 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 11252 |
| rs547839997 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961019 | CTCCCCCATTCCCCT[C/T]GGCAAGCCAGGATCT | 11252 |
| rs547844734 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921354 | ACAGTGTGAGACTCC[A/G]TCTCAAAAAAGAAAA | 11252 |
| rs547846489 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873256 | TACTGTCAAACCCAA[C/T]AGGCAGGATTGAAAA | 11252 |
| rs547894835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000846 | CTGTGTGGCACTGCC[A/G]TGATCCAATCACATT | 11252 |
| rs547951348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911956 | CTCCACCAAAAAAAC[C/T]AAAGGGCCTGCCAGA | 11252 |
| rs547956163 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891901 | ATCAGCCCTGCTTGG[C/T]CCCTGGCTAGCCCTG | 11252 |
| rs547980016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977778 | CACTTCCCCCCTCAC[A/G]CTCTCTGTCTCTCTC | 11252 |
| rs548000122 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994233 | GTTTGGTGGTAAGAA[G/T]GGCTGAGCAGGGGGA | 11252 |
| rs548002858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905889 | AATTCTGCAGCTGCT[A/G]GAACACAGCAGGAGA | 11252 |
| rs548014023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994739 | TCACACTGGAAAAAG[A/G]GCCCCGGGCAGGGGT | 11252 |
| rs548016439 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870928 | TATAACTGTACACAG[A/C]CTTTAAATTAAAAAC | 11252 |
| rs548035022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872916 | ACCGCTTCGTGCCTC[A/G]GGCCCCTGGCGTTTC | 11252 |
| rs548057946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945803 | CAGCCACTTGTTTAG[A/T]CCCCGACTCCCTTCA | 11252 |
| rs548072508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989204 | CTTAATACAATAGAA[A/G]ACTCAATTCTCGGCC | 11252 |
| rs548081719 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936833 | AGAGAATCACCTGAA[A/C]CCGCGAGACGGAGGT | 11252 |
| rs548118877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901328 | ATCTCCTCTGTCAGC[C/T]TGGCAGACAAGGATG | 11252 |
| rs548118968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894311 | AGTGGCACGATCTCG[A/G]CTCACTGCAACCTCC | 11252 |
| rs548124720 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908508 | AGTGGAAAGGCAGGA[C/G]GAGGGCCCCTGGGCT | 11252 |
| rs548132113 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940104 | GCTGTAGGCAGGAGC[A/G]GGACAATGCTTGCTA | 11252 |
| rs548167187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883743 | AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11252 |
| rs548183779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003250 | AACCTTCAATTTTTA[A/G]AAGATTTAAAGAAAG | 11252 |
| rs548191237 | in-del | -/TTAG | 0.0126979 | 0.078662 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927589 | TAGTTATTTAGTTAT[-/TTAG]TTAGTTATTTTTGAG | 11252 |
| rs548194267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963813 | GATATTTGGCAAAAG[G/T]TCGTGTCATTTGGAA | 11252 |
| rs548233789 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944153 | TGAGCAGGCCTCGAG[C/T]GGCAGCTCTCAGAGA | 11252 |
| rs548243560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970420 | TGGTGAAATCCAAAG[A/G]AAGTCCATAGTTTAT | 11252 |
| rs548253479 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015406 | CAAAGCCGCTCGCTG[G/T]TGGTGGTCCTTGAGA | 11252 |
| rs548254542 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013580 | GGGCAAGAACAGGAG[A/G]GCTGGCATTCAACAC | 11252 |
| rs548264530 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894630 | TGACTGCCTTTTTTC[A/G]TATATGAAAAGAAAA | 11252 |
| rs548285959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884122 | TGGCAGAGTGGGCCC[A/G]GCCTTATCTGCTTGG | 11252 |
| rs548291152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965062 | ATCAAAACCCAACTG[G/T]GTGTGGCATCGGCGC | 11252 |
| rs548298367 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872390 | GGACCTCGTCAGGAG[C/G]AAGCAATTGGTGGGA | 11252 |
| rs548301449 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989462 | GAGATCACACGATTG[C/T]ACTCCAGCCTGGGCA | 11252 |
| rs548304225 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016169 | ACATAGCAAGACCCA[A/G]TTCTCTAAAAAGTAA | 11252 |
| rs548306098 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923977 | AGCCCAGGAATTTGA[A/G]GCAGCAGTGAGTTAC | 11252 |
| rs548322392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878964 | CTCCCAGGTGTCCAG[G/T]CCGGGGCTGCCCTGG | 11252 |
| rs548331786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879521 | TTCCTGACCCCACCC[A/C]CCAAGGTTCTCAGTC | 11252 |
| rs548332580 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977141 | GTAATTTCATTTAGA[C/T]CATGGATGGAAGAAG | 11252 |
| rs548362401 | in-del | -/AAAAAGAAAAGAAAAGAAAAG/AAAAGAAAAG | 0.0303856 | 0.120119 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884014 | CGTCTCAAAAAAAAA[lengthTooLong]AAAAGAAAAGAAAAG | 11252 |
| rs548363693 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939062 | CAGCAGCAAAGGTAG[A/G]ACAGGCCCCAAGGTC | 11252 |
| rs548380215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891702 | TGAGCCACCGCGCCC[A/G]GCCATGCCTTTCCTT | 11252 |
| rs548386828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973817 | GGCACCTAGCACAGG[A/G]CTTAGGGTCTAGGGG | 11252 |
| rs548404914 | in-del | -/T | 0.437824 | 0.164991 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963846 | ATAAAATTTCTACAA[-/T]TTTTTTTTTCACCAC | 11252 |
| rs548416638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909220 | CATGATGACCTGCCT[A/G]GTGTCTACCTTATTC | 11252 |
| rs548416979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884910 | CCTCAAGCCTCAGAT[C/T]TGGCCCACAGCAAAG | 11252 |
| rs548432865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985071 | TGGTGGCTCACGCCT[A/G]TAATCTCAGCACTTT | 11252 |
| rs548440979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952504 | GCTGGGACTTTAGGC[A/G]CGCACCACCACGCCT | 11252 |
| rs548464362 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968285 | TTCAAGTCTGCCACC[-/T]TTTTTTTTCATAGTC | 11252 |
| rs548476661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902936 | CAGTTCTCAATCCTG[C/T]GAGTCACACGAGCTC | 11252 |
| rs548484132 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914574 | TCCTGGAGTCGCCTC[A/T]CCCCATGTTTCAGCA | 11252 |
| rs548511137 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005527 | ATATGAGGGGAGTCC[A/C]TGCAGGGCCAGGGCA | 11252 |
| rs548514458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903375 | TATGCTGAATCTTCC[C/T]TTCCAAACGGGGATG | 11252 |
| rs548522694 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942808 | TGTTTCTTGAATACT[A/G]TAGATTTATACATTT | 11252 |
| rs548591933 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889781 | TGACAGCCTCCAACT[A/G]GCCAAGGCTCGACAA | 11252 |
| rs548650265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898049 | CAGAAGGCTGGCGGG[A/G]GTGGGGACATCCTGG | 11252 |
| rs548690037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974162 | AAGTCTCCTTCCCTC[C/T]GTATCCCTATGTCGA | 11252 |
| rs548691973 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967780 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 11252 |
| rs548700791 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898129 | CAGGGCATGCGAGCC[-/A]AAAAAAGGGAGCTGC | 11252 |
| rs548702639 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874222 | AGGAGGCTGAGGTGG[C/G]AGGACTGCTTGAGCC | 11252 |
| rs548763454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982597 | CTGTGCTCTCTGAAA[C/T]ATGTGCTGTGTCACT | 11252 |
| rs548806577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881621 | GTGAGTCCTGAGATC[C/T]CCAGGCCCTTGCATT | 11252 |
| rs548826314 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892216 | CTGGAGGGAGGGAGA[A/G]CCACAACGGAGCCGG | 11252 |
| rs548836772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937108 | GACCAAAACTCCTGC[C/T]CTCATGGGTCTGTGT | 11252 |
| rs548863186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960322 | GTCCCTACATGTGGA[A/G]GTCAACTTCCTTCTG | 11252 |
| rs548866583 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916629 | CTCCCTTTCCTCCCC[C/G]AACTGCTTGCACACC | 11252 |
| rs548866889 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917268 | AACCACTGATCTTAA[C/G]CACCTCAGTGCTGAG | 11252 |
| rs548891576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005980 | TTAGTTTTTGTTGAG[A/T]TAGGGTCTCACTATG | 11252 |
| rs548895291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001601 | GCCTGTGCTTGGGAA[G/T]CAAGACACTTGTATG | 11252 |
| rs548918364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942724 | AACTGACCATAAATG[C/T]AGGGGTTTAGTTTTG | 11252 |
| rs548920146 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986055 | CTTTCCAAACAACGA[C/T]CCCCTTGCTCTGTAG | 11252 |
| rs548921756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877509 | AGGGGTTCAGGGCTC[A/G]CTCTTCTGCTCTGTG | 11252 |
| rs548956569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994983 | AACTGTGCCTTGCCC[A/G]TTTAGACTGGAAATT | 11252 |
| rs548958509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002091 | CAAGGCAAGCAAGCA[A/C]CAGTGCTATAAACTT | 11252 |
| rs548971071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995612 | TTCCAATGTCATTCA[C/T]GCGGCAATTATTTGG | 11252 |
| rs548981565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936418 | GGACTTAGCACAAGA[C/G]TCCTCCCCTCTGACC | 11252 |
| rs549004217 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010080 | TCACCATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 11252 |
| rs549010181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980058 | ACAAGTTTCTATTAA[A/T]ACAAGTTGTTAATTA | 11252 |
| rs549016976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963007 | TGCCCGACCACTCTT[C/T]AGGTGATGCTGGGAC | 11252 |
| rs549026728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894292 | TGTCGTCAGGCTGGA[A/G]TGCAGTGGCACGATC | 11252 |
| rs549027221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008731 | TCAAACCCACCCAGC[A/G]GCTCTGGGCCCAGGG | 11252 |
| rs549028278 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883863 | ACAGAAATTAGCTGG[A/G]TGTGGTGGCGCATGC | 11252 |
| rs549083607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919899 | AAGCAGGTGGATCAC[C/T]TGAGGCCACCCTGGG | 11252 |
| rs549099865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931873 | TAAGGAACACAGGTG[A/G]TATTAATAACCCTAA | 11252 |
| rs549124557 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891520 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 11252 |
| rs549157797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013692 | ATAACCGCAGAGGAA[C/G]GCACCGAAAAGGAGG | 11252 |
| rs549200335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871533 | GTGGGCTACAGAGCC[A/G]CATTCACGAGCTTTG | 11252 |
| rs549277321 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015369 | ATTTAATGGGCTGCG[A/T]GGGTGGCGCAGATTA | 11252 |
| rs549286579 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914753 | GCAGGCCCCTGCTCC[A/G]GACTGAGAGGCAGCT | 11252 |
| rs549312827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989779 | GCATTCCAGCCTGGG[C/T]GACACAGTGAGACTC | 11252 |
| rs549316334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879986 | ACTGGCTTCACCAAC[C/T]GCACTGAAAATGGAC | 11252 |
| rs549362421 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938581 | AAGCAGAGGCTGTCC[-/A]AACATGAAGAATGCC | 11252 |
| rs549377271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909541 | GAGAAGGCGGACGAC[C/T]ACAGCACTGCGGAGT | 11252 |
| rs549423561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989991 | AGATATATTTATATA[C/T]ACATATATACACACA | 11252 |
| rs549426836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955492 | AAAAAAAAAAAGGCT[A/G]TCAGGTGCTGGGACA | 11252 |
| rs549432958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890392 | GCTCTACCACCAATG[C/T]ATGGTTCTGATCCTC | 11252 |
| rs549440227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909922 | CGACTCCCTCAGCTC[C/T]CGTGTCAGAGGGAAG | 11252 |
| rs549458565 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934049 | CAGTTCTTTAACACA[C/G/T]TTGTCTTCCAGGCTT | 11252 |
| rs549473394 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939591 | ACTCCCACAGGGCAA[C/T]GTTTTTAACAGAAAT | 11252 |
| rs549476260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950647 | GTAACATTCAACGCC[A/G]TAAGTAGCATTCTTA | 11252 |
| rs549507161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938220 | TGTTTCCTGGGCTCG[C/T]GAAGCAGCAGAAGGT | 11252 |
| rs549537325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944294 | TCTCTGAGACTTGGG[C/G]TTTGCTTGTTACTGC | 11252 |
| rs549554669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904109 | CTAACTCCAAAGGCA[A/G]AACACATAAGATAGA | 11252 |
| rs549570945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932583 | GATATCAAATAAGAC[A/C]TTTAGGATAATGTAC | 11252 |
| rs549583440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934994 | AATCTCGGCTCACTG[C/T]AAGCTCCACCTCCCA | 11252 |
| rs549637764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974956 | GCAAGGATATCTCCT[C/T]TGCAGACCCAGCTGA | 11252 |
| rs549713272 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969951 | AAGAAACTAGAATGA[A/C]CCCCCGTTTCAACAA | 11252 |
| rs549721919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959672 | CTCTAAAACTAGGTG[C/T]GCTTGCATAGAAGGT | 11252 |
| rs549748391 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964058 | AAAGAGAAACCCTGT[A/G]CCCTTTAGCTATCAT | 11252 |
| rs549748504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922623 | TCCTCTTCACTATCT[C/G]GGGGGAGATTCTTCA | 11252 |
| rs549755033 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929865 | TCAGATGCCACCTCT[G/T]TCATAAAGACTTCCT | 11252 |
| rs549760866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916599 | TCCTGGCTCCCCGCT[C/T]TCACCCTGACAAGCC | 11252 |
| rs549766561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923401 | CTCCACTAAGCTACT[G/T]CATCTTCAACTATTT | 11252 |
| rs549836459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874632 | TTCTCTGGCAGTTGG[C/G]GACCCCTAGAGAAAG | 11252 |
| rs549881880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952917 | GTGATCCACTGGCCT[C/T]GGCCTCCCACAGTGT | 11252 |
| rs549901525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012075 | ACTTGAACCTGGGAG[A/G]CAGAGGTTACAGTGA | 11252 |
| rs549925647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006135 | GAGCTCTCTCGCCTT[A/C]TTTCTGTCATGTGAA | 11252 |
| rs549927482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954439 | TGTCCCTCTGTCATT[C/T]AGGCTGAGTGCAGTG | 11252 |
| rs549932425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993100 | AATCACTTCAACCCG[A/G]GAGGCGGAGGTTGCA | 11252 |
| rs549942134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966402 | TTTACTCATCCAACA[C/T]GTGTACATAAAAAGG | 11252 |
| rs549943264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42947015 | CGACGCCTCCTCTCC[A/G]TCAGAGGCACCTGCC | 11252 |
| rs549967866 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007307 | CTGCAATCTCTGCCC[C/G]CAGGTTCAAGCGATT | 11252 |
| rs549970721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917173 | AAAGCAAGGAACCTG[A/G]GGCATACAAAGGGTT | 11252 |
| rs549994417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986626 | ACTAAAATCCACATG[G/T]GAACACAATGACTTC | 11252 |
| rs550050069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893145 | GTGCCAAGCGGCAAG[A/G]CCTTCCACGTGATAG | 11252 |
| rs550121070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932445 | CTCTAGACAGTGAAT[G/T]CCAGAAGCGTATCTC | 11252 |
| rs550121198 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003075 | CCTCGAAGTGTTGCC[C/T]TGAGGCAGGACAGAG | 11252 |
| rs550123979 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012896 | CGACCTCTGGTGATC[C/T]GCCCGCCTCTGCCTC | 11252 |
| rs550147145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978012 | GTCTGAAAAAGACTA[C/G]AGCAATTCAGTGTGA | 11252 |
| rs550152111 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000397 | TCCCAATGGACTGAG[A/T]TTGTCTCCACCTCCA | 11252 |
| rs550165919 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984304 | TAAATAAAATTCTTC[C/G]TGCCCTCAATGAAAA | 11252 |
| rs550173656 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987643 | TTCAAGCGATTCTCC[C/T]GCCTCAGCGTCCCAA | 11252 |
| rs550182277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933204 | TAAGAAATTGGAAAC[A/G]AACTATCTCTATGGT | 11252 |
| rs550191695 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936195 | CACTCCAGCCTGGGC[A/G]GCAGAGCGAGACTCC | 11252 |
| rs550228365 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934402 | TGGCTTCTGTGTACT[-/C]CCCCTCCTTTGGGCC | 11252 |
| rs550235299 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010159 | AGGTGTGAGCCACAG[C/T]GCCCAGCCCCATTTT | 11252 |
| rs550236940 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870470 | TCTCTGAATATCAAA[A/T]AATATATACAGATAG | 11252 |
| rs550245397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942174 | GCTCAGGCTGGTCTC[A/G]AACTCTTGGCCTCAA | 11252 |
| rs550279117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006971 | CTTCCTAGGAACACA[G/T]ATGGCAATCCTTGAG | 11252 |
| rs550302483 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980481 | CCCTCTCCCTCTCCC[C/T]CTCCCCCTCCCCCTC | 11252 |
| rs550304522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875826 | ACAGGCGTGAGCCAC[C/G]ATGCCTGGCCTAATT | 11252 |
| rs550315950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880811 | AATAGTCCTCCCCAC[C/T]GTGCCCCTCTTTGGG | 11252 |
| rs550336603 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015311 | GGGAAAGCCCCAGGA[A/C]GCGCATTGGTGACTT | 11252 |
| rs550398007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969887 | TAGCCTGAGTGACAG[C/G]GTGAGATGCTGGCCC | 11252 |
| rs550412479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963707 | CTAATAAGGGCAGAA[C/T]GGGATTCAGTCAGGT | 11252 |
| rs550420753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009713 | TCTTGGGAGGAAAAA[A/T]AATCATATAAATTTT | 11252 |
| rs550443859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958244 | GACCTTGGACAAGTC[A/G]TCACCTCTGGATCCC | 11252 |
| rs550453378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878297 | AAAGCAGCGGAATGA[C/T]GACAGCCACACCTGC | 11252 |
| rs550466047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994116 | ATCCTTCTGATATTG[C/T]GCCAGAATGCTAACA | 11252 |
| rs550502238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920673 | ACCAGGAGAAGAAAA[A/C]CACCTAAAAACGCCA | 11252 |
| rs550503828 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951807 | CCCTGATTACAAGGT[C/G]CCATGTGATTCTAGC | 11252 |
| rs550506975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900061 | TCTGTGAAGTCTTGG[A/C]TCCTTTTCCCCACGC | 11252 |
| rs550566616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995055 | TCCAACAATCACATA[A/G]TCAAAGGGGACAATG | 11252 |
| rs550572747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926293 | CACACTGAGGCCTAG[A/G]GCTCAGCAGGTCCTA | 11252 |
| rs550582987 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969300 | ACATTACATGGTAAA[C/G]TTTCTTTGTATTCTA | 11252 |
| rs550622584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976430 | ACAGACTGGCTCCTC[G/T]CCCCAAAAGCCTGAC | 11252 |
| rs550678694 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950314 | ATTTTGGTATCCTTT[C/G]GAGGGTCCTGGAACA | 11252 |
| rs550715927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939211 | CACATCAGCTGACAG[A/G]TCCAGACTTGCCTTG | 11252 |
| rs550736273 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999298 | AAGTACCTCGAAGGG[G/T]TCCAGGGAACTCTCC | 11252 |
| rs550742509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984980 | GGATTTGCTTGTTCT[C/G]TTTGGCAACCAAAGG | 11252 |
| rs550762752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897063 | CACCTCAGCCTCCAG[A/G]GTAGCTGGAACTACA | 11252 |
| rs550772294 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918817 | GGCGCTGGGCCTGTC[A/C]GGAAGTACTACTATA | 11252 |
| rs550789503 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971203 | TGATTCTCCTGCCTC[A/G]GCCTGCCAAGCGCCT | 11252 |
| rs550800307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891587 | TTGTATTTTTAGTAG[A/G]GACGGGGTTTCACCA | 11252 |
| rs550837218 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884850 | TTGAGCGTGCCACAC[A/G]CCCATGTCCTCTTCT | 11252 |
| rs550858832 | in-del | -/T | 0.433382 | 0.169915 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927250 | GTATCTTCCAGTTAC[-/T]TTTTTTTTTTTTTGA | 11252 |
| rs550871395 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875432 | TGGAGTATAGTGGTA[C/T]AATCATGATTCATTG | 11252 |
| rs550877009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872879 | ACAGGGCAGCAGCCA[C/T]GATGAACCACCATCT | 11252 |
| rs550895382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945140 | TGTCATCTCCGTATC[C/T]CCAGTGCTTAGCATG | 11252 |
| rs550924432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010880 | GAAAGGTGGTTTTTA[C/T]TTGTTTTATGTGTGC | 11252 |
| rs550936968 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870044 | CGTTCCCCCCACCCC[C/T]GCCGGCCCGCGTGGC | 11252 |
| rs550942406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902315 | CCACGGAGAGTGAGC[C/T]GGGGGCTCTGCTGCC | 11252 |
| rs550978772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908318 | CAGAGATGCAGGCAG[C/T]GGCTCTCAGCCCTGC | 11252 |
| rs550987754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964910 | AGACCCATGGCTTGG[A/T]TAAAAAGAAGATTCC | 11252 |
| rs551004212 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879487 | TGGCGAGGACCAGGG[C/G]AAGGTCCGGGGCCTC | 11252 |
| rs551006481 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005324 | GGCTTTCTAGAATCC[A/G]TCACATTAAACTCAG | 11252 |
| rs551009732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985434 | ACAAGGGCAGCAGAT[A/G]GGCACACTCCAAGGC | 11252 |
| rs551022962 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987908 | CACTTTGGGAGGCTG[A/G]GGCGGGCAGATCACT | 11252 |
| rs551026562 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921949 | TCGCCATGTTGGCCA[G/T]GCTGGTCTCGAACTC | 11252 |
| rs551054858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897768 | GAGAGGTATCCTGAA[C/T]GCAATATCCAAAGGG | 11252 |
| rs551060942 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015939 | TGGAGTAAAGAGAGT[A/G]AATGGCAGAGCCAGG | 11252 |
| rs551066832 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974836 | AGAAGAAGAAGAGGA[A/G]GAGGAGGACGAGGAG | 11252 |
| rs551067771 | snp | A/G | 1.66813e-05 | 0.00288797 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42893521 | CGCATACGCCTTCTC[A/G]ATGCGCGCCCGCTCA | 11252 |
| rs551081557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904698 | CGTTCCCTCCTCTTC[C/T]CAGTTTGGTGCTTCC | 11252 |
| rs551083334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940007 | CTACCTAGCACCAGA[C/T]ACAATTACTGGGTTT | 11252 |
| rs551085213 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936836 | GAATCACCTGAACCC[A/G]CGAGACGGAGGTTGC | 11252 |
| rs551109011 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954405 | AAGTGAGAAACTGAC[-/T]TTTTTTTTTGAGACA | 11252 |
| rs551187427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934391 | TTTTCCCTTCTTGGC[C/T]TCTGTGTACTCCCCC | 11252 |
| rs551194160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900498 | TTTTATTATTTTATT[C/T]GCGAGAAGGGTCTCA | 11252 |
| rs551199563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928306 | ATCTGAGAGTGCTGT[A/C]GGCGATGAAATATCA | 11252 |
| rs551233526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997514 | AGTGAGCTGAGATGG[A/C]GCCACTGCACTCCAG | 11252 |
| rs551242047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888029 | GACAAGCGCTCCCAG[C/G]CTGCAGTCCCTCCCC | 11252 |
| rs551274587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011430 | ACATGAAGGTGGCCA[A/G]AGAGCATCTGGTAAA | 11252 |
| rs551293480 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004394 | TCCTTGGTGGCACAT[A/G]CCCAGTCTCCTTATC | 11252 |
| rs551294172 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913894 | ATCAGGCTTCCTACA[A/G]CCTAAAATTGGATTG | 11252 |
| rs551304311 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959167 | CCTGGAGCGGTGGCA[C/G]GTGATCAGAGACTCT | 11252 |
| rs551307789 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883767 | TCCCAGCACTTTGGA[A/G]GGCCGAGGTGGGCGG | 11252 |
| rs551325750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948168 | CCCAGTGCAGGGTCC[C/T]GCTGGTCCTGGAGGG | 11252 |
| rs551343973 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993715 | TGGCAGGAATGCCCC[C/T]GAAGGCCGACCAGAG | 11252 |
| rs551356795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000884 | TTCCCATGGCTTACA[G/T]GTGGTCAGGAGTACC | 11252 |
| rs551379685 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911158 | ATCCACCCGCCTCGG[A/C]CTCCCAAAGTGCTGG | 11252 |
| rs551402884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013650 | GGCAATCCCAGGAGG[A/G]TTAAAACAGAACTTC | 11252 |
| rs551421808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899941 | ACAAAAGCTGTAACA[C/T]TAGAAATGGGGAGGG | 11252 |
| rs551439489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881985 | TTCAGGAGAGGTTCA[A/G]AAGGCCTTCGGTAAT | 11252 |
| rs551440137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942159 | ACAGGGTCTCATGTT[C/G]CTCAGGCTGGTCTCA | 11252 |
| rs551480116 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953129 | ATTTAAAAAAATCAG[-/A]AAAAAAAAACTGGAC | 11252 |
| rs551494848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919271 | GAGCCACTGTCCTTG[A/T]CTGTAAGGCAGTACA | 11252 |
| rs551564440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930747 | TTTTGACAGTTCAAG[G/T]TCAAAAGTAAATTTA | 11252 |
| rs551586309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973373 | GACGAGCAAAACACA[A/G]GTCAAAACTTCCCCA | 11252 |
| rs551588496 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907156 | GGTGGCTCAGCTTGG[C/G/T]TGGAGCCCAGGGCAG | 11252 |
| rs551626410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931193 | GGGCACAGCACCTGG[C/T]TTACACGAGGCAATG | 11252 |
| rs551648414 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889805 | TCGACAAAACTCAAT[A/G]GCTTTGGTTGCTACT | 11252 |
| rs551653861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950569 | TGAAGGCCTGTGCAG[C/T]CACCATTGCTGAAAC | 11252 |
| rs551668093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881562 | ACCTTTGCCCACTGC[C/T]TTCAGGGTGCCAGGT | 11252 |
| rs551690545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924766 | TTTTTTTTCTTTTTT[C/T]TTTTTTTCGACACAG | 11252 |
| rs551704164 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938072 | TCTAGATGACAGCCC[A/T]AAAAACGACTGCCAT | 11252 |
| rs551706698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876428 | ACTGGAGCCTTGGGG[A/C]TCAGGGCTGAGGGCT | 11252 |
| rs551736365 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989891 | ATATATATATACACA[C/G]ACACACACATATATG | 11252 |
| rs551750099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918697 | GCAATCTCTGGCAGC[A/G]AAAAGAAGAAAGGGC | 11252 |
| rs551767721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955313 | AACAAACAAACGAAC[A/G]AACGAACGAAAAAAC | 11252 |
| rs551793354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895552 | AGGGAAAAGAAAAGG[A/G]TATTTCTTAACAAGT | 11252 |
| rs551823544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994801 | TATGAAAGGTCTGGG[A/G]GCTGCGGGGAGCACC | 11252 |
| rs551836944 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975389 | TTTGGGAGGCTGAGG[C/G]AGGAGAATTGCTCGA | 11252 |
| rs551848545 | snp | A/G | 8.65628e-05 | 0.00657829 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879008 | CCCAGGGCCCCCACC[A/G]TGGAACGGCCTCTTT | 11252 |
| rs551864941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955338 | AAAAACAAATCAACT[A/G]ATCCAGCCAGCCAGC | 11252 |
| rs551893810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949836 | TTTAATTTATTCTAA[C/T]AAACTGAGTAAATAT | 11252 |
| rs551894587 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870595 | TGTTAATTTGCAAAA[A/G]AGTACAGTTTTAAGC | 11252 |
| rs551906021 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943576 | TGGTTTGCTGAGTGT[C/T]TCTGTCATGAAGAGG | 11252 |
| rs551932788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989450 | TTGCAGTGAGCCGAG[A/G]TCACACGATTGCACT | 11252 |
| rs551960675 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997859 | GCACCCCAGCCTGGG[A/C/T]GACAGGGCAAGACTC | 11252 |
| rs552018489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894925 | CAGAGATGGGCAAGG[A/G]GAGGGAAGGGGGCTG | 11252 |
| rs552058586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946529 | CACTCCAGCCTGGGG[A/G]AAAGAGCAAAACTCT | 11252 |
| rs552085185 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969956 | ACTAGAATGACCCCC[C/T]GTTTCAACAAGTATC | 11252 |
| rs552110180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934979 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 11252 |
| rs552116281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903502 | TTCAGGTGCCAAACT[A/G]CAATTTCCACATCCT | 11252 |
| rs552121695 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974846 | GAGGAGGAGGAGGAC[A/G]AGGAGAAGGAACAAC | 11252 |
| rs552127561 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002692 | AAGATTTCTATTCTC[A/G]GGAATTTATCCCCAG | 11252 |
| rs552147870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004153 | GGTGAAATGAGTGTG[A/G]GCTTCGGTAGGCAGA | 11252 |
| rs552159863 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921899 | GCTCACCACCATGCC[A/T]GGCTAATTTTTGTAT | 11252 |
| rs552177856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935215 | TAGGCGTGAGCCACC[A/G]TGCCCAGCCCAGGGC | 11252 |
| rs552185163 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926481 | ATGGCACAGAACTAT[A/C]CACTGCAAACTGAAG | 11252 |
| rs552195988 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947143 | AAGATTCTCCTGGCA[A/T]AAATAGAAGGAAAAA | 11252 |
| rs552202161 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015647 | TTTAAACGGGGGGTT[-/G]GGGGGGGCGTATGTT | 11252 |
| rs552230099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964774 | CCACAAGCCTTTTCC[A/G]TTAGGAATTTGTAAC | 11252 |
| rs552232064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958470 | TCATACCTGTAAAAA[C/T]GCTTTGGTTTGAAGT | 11252 |
| rs552243949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952055 | CCCAGCCCTGATACT[A/C]CAGCCCTAACTCTGT | 11252 |
| rs552247994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879357 | ACTTATGAACCCAAA[C/T]GACCTGAGCCCCTCC | 11252 |
| rs552281388 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017112 | TGATATCGCGCCACT[A/G]CACTCCAGCCCGGGC | 11252 |
| rs552293610 | in-del | -/T | 0.444799 | 0.156695 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875541 | AATTAGCCCAGCTAA[-/T]TTTTTTTTTTTTGAC | 11252 |
| rs552301099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873087 | CTGGGAGCTAATTTT[A/G]CATTGTTAAAAAGCA | 11252 |
| rs552314119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929139 | TGACGGCCGCCCTGT[A/G]CAACTATACTCACCA | 11252 |
| rs552320130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952805 | GTAGCTGGGATTACA[A/G]GTGTGTGCCACCAGG | 11252 |
| rs552334426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998464 | AAACACAGAGCAAGA[A/G]AAGGGCAACAATAAA | 11252 |
| rs552345936 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902310 | GAGGCCCACGGAGAG[C/T]GAGCTGGGGGCTCTG | 11252 |
| rs552367697 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885524 | GAGGAAGGATGGAGC[A/G]CTTCCCGAGACACTG | 11252 |
| rs552385331 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968310 | ATAGTCCCTAATAAC[A/C]AACTCAAACCCTTAG | 11252 |
| rs552385717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965974 | TGTGAAAATGTGATA[A/G]GTCAATCTTTTTCAT | 11252 |
| rs552397376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992574 | GCAACATAGGGAGAC[C/T]CTGTCTCCATTAAAT | 11252 |
| rs552406146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880077 | GCAGGTGTTTAATGA[A/G]CTCTCCTTCCCCCCA | 11252 |
| rs552421216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897001 | GAGTGCAGTGCCACA[A/G]TCATGGCTCACTGTG | 11252 |
| rs552429927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42946978 | GATCATGCCAGAGCA[G/T]CCACGGCCACATACT | 11252 |
| rs552447387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985561 | GACACTGCCTCCAGC[C/T]CTCGCTCGGCCAACC | 11252 |
| rs552448070 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992885 | AGAATATATACTGGC[A/C/T]GGAAGTGGTGGCTCA | 11252 |
| rs552455545 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941370 | TGTGTACAAGCCTTT[C/G]TATGGACAGATGTTT | 11252 |
| rs552456440 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894902 | AAATCTCTTTGCCTG[G/T]CCCTGCACAGAGATG | 11252 |
| rs552460269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954297 | AGGAAGGTTCCCTTG[A/G]ACAGAGAGTGGAGAA | 11252 |
| rs552461228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986221 | TAACAAAAGAGAACT[G/T]GACCAACAGAAAAGG | 11252 |
| rs552520969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977780 | CTTCCCCCCTCACGC[G/T]CTCTGTCTCTCTCCT | 11252 |
| rs552525378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942023 | CTCAGGTGATCTGCC[C/T]GCCTCTGCCTCCCAA | 11252 |
| rs552532058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967493 | GAATCAATGAAAAGC[C/T]TTAAACTAAAGATCT | 11252 |
| rs552567880 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017520 | GGTTTCTGAACAAGC[A/G]TCTGTCATCAGGCCT | 11252 |
| rs552568429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993253 | TTTAGAAAATGCAAA[C/T]GATTCTACAGTGGCA | 11252 |
| rs552568707 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947802 | GGATCAAATGGCATC[C/T]GGCTGGGACCTGGCA | 11252 |
| rs552593112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961320 | AACACTGCGGAAGGC[C/T]GCAGGGTCCTCTGCC | 11252 |
| rs552596133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972008 | CCCCGTCTGGGAGGT[A/G]TACCCAGCAGCTCAT | 11252 |
| rs552596165 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931764 | CCATGCAGAGATCAC[A/G]TTGTTATTATTATGG | 11252 |
| rs552603662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961926 | CCCGTCACCAAAAAA[G/T]CAGAGAAGTCAACAC | 11252 |
| rs552607922 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926066 | AGCTGGGATGTTTTT[A/T]AAGAGCTCAACTACC | 11252 |
| rs552629147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875650 | AAGTGATTCTCCTGC[C/T]GCAGCCTCCTGAGTA | 11252 |
| rs552631855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011599 | CACAGCACAGACTTT[C/G]AAGGTATAGAGAAGA | 11252 |
| rs552651724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931363 | TTGTTGGAGGACTGA[A/G]GTAGCTGCTTTCCAC | 11252 |
| rs552670956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929702 | TGGTCTACTTCAACT[C/T]GGACAAGGCAGGAGA | 11252 |
| rs552672214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973687 | CATAAACCCAGACTG[C/G]GTTGGCTGCTCTCCC | 11252 |
| rs552675404 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876608 | ACAGACTGCGCGTTG[G/T]CTGTTTTCCTGTCAT | 11252 |
| rs552681297 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902352 | CGCTTCCCCCACAGA[C/T]TACCCCTCCCCCTGG | 11252 |
| rs552686949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893022 | CACCTGTAATTATTC[C/T]CTTAAAATGTAAACT | 11252 |
| rs552710163 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870800 | CTGAGGCTAAGCCTA[C/T]ACACGGCGTGGCTGA | 11252 |
| rs552713007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924916 | TGCCTGCCACTACGC[C/T]CAGCTAATTTTTTAT | 11252 |
| rs552719594 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012006 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGATGCCT | 11252 |
| rs552732342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923333 | TGGTCTTAAGTCCCT[C/T]GTGCAGAGTAAAAGC | 11252 |
| rs552740061 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932751 | TACAAAGTCAATTCT[-/A]AAAAAAAAAAAAAAG | 11252 |
| rs552748970 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007745 | AGTTTCCAGGCCTGC[C/T]GCCTATACTGAGCTG | 11252 |
| rs552778382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881710 | TTTGAATCAGGATTC[A/C]CTGAATTTACTGCCT | 11252 |
| rs552804293 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870362 | GCCAGCCAGACGTGT[A/G]CCTGAATGCCACAGA | 11252 |
| rs552811743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917103 | GCACTACACGCGTGC[A/G]CTCCATTTAGTCCTA | 11252 |
| rs552822114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989563 | GCACCTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 11252 |
| rs552833017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875199 | TCTCTCTTCTAGGCT[A/G]GAGTACGTGGTATGA | 11252 |
| rs552876680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917731 | TCTTGGCCTTTCAGA[A/T]GATGTTAGTAAGCCA | 11252 |
| rs552934957 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983059 | CAGTGGCTTACAACT[A/G]TAATTCCAGCACTTT | 11252 |
| rs552947871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906779 | CCAAAATAAGCATAA[G/T]AACCTTAAACGAAGA | 11252 |
| rs552957447 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927506 | CACCCATCTTGGCCT[-/C]CCAAAGTGCTGGGAT | 11252 |
| rs552996541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983618 | TAAAAGATTGACATA[G/T]GAGAATATATCAATT | 11252 |
| rs553014218 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000527 | ATGTTAAACTATTTC[G/T]AAATTTCGTGAACCT | 11252 |
| rs553015049 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889505 | AGACAGTTTCATTAT[A/G]AATGGGGCCAGGGAC | 11252 |
| rs553053129 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955477 | GATAGCATCAGGGGG[A/G]AAAAAAAAAAGGCTG | 11252 |
| rs553085368 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970774 | GGAAGGCAGGGCCCC[A/G]TGTAAGCTGATGTCA | 11252 |
| rs553134712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918999 | GCTCTGCTTCATTCA[A/T]TCTTCCAGGTTGAGC | 11252 |
| rs553141630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009242 | CCATCAACGTGCTGA[A/C]CAAGCCTGGCCCACT | 11252 |
| rs553149497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906227 | ATGAGCCTGACTGAC[C/T]GACCAAGGGGGACAA | 11252 |
| rs553165785 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949365 | AGGATATGGCTTTGG[A/C]AAGCAGGACTTACAC | 11252 |
| rs553178389 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009933 | GGAGTGCAGTGGCAC[A/C]ATCTCGGCTCACTGC | 11252 |
| rs553191936 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898997 | GCATGCATCTGTTGT[A/T]AACAGTCCAGAGGTG | 11252 |
| rs553229594 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993136 | TCGAGATTGCACCAC[C/T]GCACTCCAGCCTAGC | 11252 |
| rs553235897 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932816 | AGAGCCACTAAGTCA[A/G]AAGCACTTCCCACCT | 11252 |
| rs553243357 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901631 | GGGTTTACACTGCAC[A/G]GTAGGTTTCTTCCCA | 11252 |
| rs553258818 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015941 | GAGTAAAGAGAGTAA[A/G]TGGCAGAGCCAGGAT | 11252 |
| rs553277754 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875816 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 11252 |
| rs553284281 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943322 | CTTTATATAAGATCA[C/T]GCCATCTTTGAACAG | 11252 |
| rs553284935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913678 | TTGCCACTATTATTA[C/T]TGCATAGTAATTATG | 11252 |
| rs553305852 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987530 | ACGGGCACATTCATT[-/C]TTTTTTTTTTTTTTT | 11252 |
| rs553310437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943847 | GTGTCCAAAACTTAC[A/G]TTAAACTTTTGCACA | 11252 |
| rs553346220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903715 | GTGATGCTATTTACC[C/T]TGCAGGGCCCAAGAG | 11252 |
| rs553372901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937695 | CACTTCCCCTAACTC[A/G]GCTCTCCCTCAGACT | 11252 |
| rs553378372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974652 | TACTCGGGTGGCTGA[A/G]GCACCGTAACTGCTT | 11252 |
| rs553382873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898421 | GGATTACAGACATGC[A/G]CCACCACGCCCAGCT | 11252 |
| rs553386221 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017241 | TCTGATGCCCAGGCT[-/G]GAATGCAGTGGCACA | 11252 |
| rs553390430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968706 | CCATCCAATCTGCCG[A/G]GGGCCTAAAAAGAAC | 11252 |
| rs553416415 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914023 | TTCAAAGCCAAGTCC[C/G/T]CCAAAGACATTGCCG | 11252 |
| rs553419073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932057 | ACATCACTTCAACCC[A/T]AACTCCTCCGCTGTA | 11252 |
| rs553435353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882471 | GGAAGGTCACGGGCC[A/G]CCACGTGCACAGATG | 11252 |
| rs553449662 | in-del | -/TC | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009862 | CATCATTTTATTTTT[-/TC]TATTTTTTTTTTTTT | 11252 |
| rs553452120 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017327 | CCTCCCAAGTAGCTG[C/T]GACCACTGGTGCGCA | 11252 |
| rs553477949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985854 | ACAGTCTCATCTCCA[A/G]CTGAAGTGATTCTCC | 11252 |
| rs553480464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925887 | TCCCTGGGCCCTCTA[C/T]GTCACCAGCCTTGGC | 11252 |
| rs553485684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938231 | CTCGCGAAGCAGCAG[A/G]AGGTATGAATAGAGA | 11252 |
| rs553486033 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917932 | CCTGGCTATGCTCTA[C/T]CTTTTTATGCCTTAA | 11252 |
| rs553536836 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898307 | AGACAGTTTCGCTCT[C/T]GTTGTCCAGGCTGGA | 11252 |
| rs553555633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892148 | GGCTCAGGAAGGAAG[A/C]CCTAATCCAGGCTGG | 11252 |
| rs553571050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922884 | GCACCAGGACACAGA[C/G]AAGTAGGGCACTCTA | 11252 |
| rs553576900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012130 | GCCCGGGCGACAGAG[C/T]GAGACTCTGTCTCAA | 11252 |
| rs553624749 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875590 | ACCCAGCCTGGGGTA[C/T]AGTGGTGTGACCTTG | 11252 |
| rs553645950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963410 | AGGCGGCAAACAACA[A/C]GCAGGGCAGCACTTC | 11252 |
| rs553647719 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951050 | GAACATCTCTGGGTG[C/G]TGGAACATGAAAGTC | 11252 |
| rs553651459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878502 | TAATGACCACAGTGC[C/T]ACCCTTATATCTCTC | 11252 |
| rs553658467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956913 | ATCAAATGTTACTTA[C/T]AGACTGCAGAAGATA | 11252 |
| rs553683693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923467 | GAGTTTCACTCTGTT[A/G]CCCAGGCTGGAGTGC | 11252 |
| rs553709611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005759 | TGCTGGGCTCCTGGG[A/G]TCCATCACCTCATGC | 11252 |
| rs553736572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960112 | GAACAAAATTCATAC[C/T]ACCCCCTCCCCAACA | 11252 |
| rs553779545 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897911 | GGGGCCCTGAGAGAA[G/T]TCAGCTGGGAATGGA | 11252 |
| rs553803627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953369 | AGAATAAAAATCTCA[C/T]CAGAAGAACTACAGC | 11252 |
| rs553837698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892568 | GTGGAAACGAAATGA[C/T]GACACTGCCACCGAC | 11252 |
| rs553847254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947855 | TTCCACAAGCATTGG[C/T]CAGGGAGAAGGTGAC | 11252 |
| rs553870962 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971375 | TGCAGACGGAGTCTC[A/G]CTCACTCAGTGCTCT | 11252 |
| rs553958096 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011172 | TATGTGAGGGATCAG[C/T]GCCCTGGCCATAAGG | 11252 |
| rs553991203 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971803 | TCCGGGAGGGAGGTG[A/G]GGGGCAGCCCCCGCC | 11252 |
| rs554030661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936062 | ACTAAAAAAAATACA[A/G]AAAATTAGCCGAACA | 11252 |
| rs554050597 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960114 | ACAAAATTCATACTA[-/C]CCCCTCCCCAACACA | 11252 |
| rs554050806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966098 | CATCTTGGGCTGGGC[A/G]CGGTGGCTCACGCCT | 11252 |
| rs554054842 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986791 | CAGCAGCTACTGCAT[C/G]AACACTTGTCTCTCT | 11252 |
| rs554063157 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978940 | GTCTATGAGGTCACT[C/G]CACCCAATGTCTTCC | 11252 |
| rs554104649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008091 | ATTGAGTGATGCCTG[C/T]TGTGTGCAGTACTAT | 11252 |
| rs554125546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960563 | AATTTAAAGTGAAGA[A/G]AAAAACAATAAAGCT | 11252 |
| rs554132121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874912 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 11252 |
| rs554134993 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920309 | GCAAGATGAATCAGA[A/C]GCATGCCATCCGAAT | 11252 |
| rs554135120 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869642 | TTGGCAGGGGCAGTG[C/G]GCCGTGGCCTTTTGG | 11252 |
| rs554135594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999345 | AAATGTCTAATGTGT[A/G]TGTGTATGTGTGTGT | 11252 |
| rs554170994 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948256 | AGGGCGCTGAAGATC[A/G]GACACCAGCTCAAGT | 11252 |
| rs554194921 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904882 | CTCCGCCCCCCTGCA[C/G]TGTGCCCAGCTCAAA | 11252 |
| rs554240903 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969818 | TGCACAGCTGTGGTC[C/T]CAGCTACTCAGGAGG | 11252 |
| rs554243168 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950986 | ACAGAGAGTGACAGG[G/T]TCTACCTGGACATAT | 11252 |
| rs554247363 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871050 | CAGTGTAACCCACCA[C/T]TGACTCGGAAAGGAG | 11252 |
| rs554255745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951425 | GACCTAAAATTCCAT[C/T]CACGTGCTGATGCCT | 11252 |
| rs554259242 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895982 | GCAAAGCACTGCAGT[C/T]GTCCCAGGAGCAGAG | 11252 |
| rs554287414 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984411 | CCCGGAAGAAATGCT[C/G]TAGGCCCTCGGCCTC | 11252 |
| rs554326597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907604 | AAGTCCGTTGGGGTC[A/G]GCGTGCGTGGAGGCG | 11252 |
| rs554334390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993812 | AGGGACAGCCATGTG[C/G]GCTGTGGGACCCAGA | 11252 |
| rs554334496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986909 | CCTTTGATAGCCACT[A/G]CCTATATAATAAAGC | 11252 |
| rs554358133 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894432 | ATTTTTAGTGGAGAC[A/G]GGGTTTCACCATGTT | 11252 |
| rs554380921 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932956 | AATCAGAGGAACCAA[C/G]TGTGTTAGGAGACGA | 11252 |
| rs554401852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899652 | TAAATCATAAAGCAT[A/G]CAAGTGCCCTACGAT | 11252 |
| rs554411534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972973 | GGATTTTCTAATTAC[A/G]AACAGCATGTGAGGA | 11252 |
| rs554417237 | in-del | -/GATT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969584 | ATCCAAGCAATATGG[-/GATT]GATTATCGCTGTAGA | 11252 |
| rs554438670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900243 | TCCCCATGCCCTTCG[A/G]GTCACAGCTCGTCTC | 11252 |
| rs554456328 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887555 | CGTCTCTCTCTGCAA[A/C]TCCTGGTTGGGAATC | 11252 |
| rs554467770 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984469 | GAACCTAGTAAAACA[C/G]TGGTCCCATCTTGCA | 11252 |
| rs554479347 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887231 | CCCAGAGGATTCTGA[C/T]ACTTGGTCTGAGTGA | 11252 |
| rs554490052 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879494 | GACCAGGGCAAGGTC[C/T]GGGGCCTCCTGTTCC | 11252 |
| rs554495003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930955 | GGTGAGTCACGTGTG[C/T]GTGACTCTGAAGAGT | 11252 |
| rs554505688 | snp | C/G | 2.11707e-05 | 0.00325345 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871329 | GGGCCCGCCGCCTCC[C/G]TCCCCCCGCTGGCCT | 11252 |
| rs554523330 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970221 | CGACTAAAGTAAACC[C/G]GCAAGGTTAACATCA | 11252 |
| rs554542030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912795 | TGACCTGTCCGCAGC[C/T]GAGATGAAACTGTCT | 11252 |
| rs554553332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938745 | TGGAGCTCCACGAGG[A/G]AAGGGCTTCACCCTT | 11252 |
| rs554574050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890734 | AATAAAAATAAAAAA[C/T]TTAAAGAATGCACAT | 11252 |
| rs554582455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970765 | ACCTGGAAAGGAAGG[A/C]AGGGCCCCGTGTAAG | 11252 |
| rs554614770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933696 | ACAGCCCCCGCACCC[C/T]GCACCGTCCTTCACA | 11252 |
| rs554620316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995899 | TGAGACCTGCCCCCT[G/T]CCCCAGTCTCCAGAA | 11252 |
| rs554664272 | snp | C/T | 0.000149816 | 0.00865366 | missense | PACSIN2 | GRCh38.p7 | 22:42879160 | TTCGATTCAGGTCTG[C/T]GGACCACTCCTAGGC | 11252 |
| rs554701332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873333 | AACCCCAACCAAAGA[C/T]ATCAGAAACTGGATG | 11252 |
| rs554702552 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906238 | TGACTGACCAAGGGG[A/G]ACAAAGGACAGCTTG | 11252 |
| rs554739720 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909754 | AATATACACTGGCAA[C/T]GTTCACCTGAATGTT | 11252 |
| rs554740911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010583 | AGTGTGGCGGCGGGC[A/G]CCTGTAGTCCCAGCT | 11252 |
| rs554741794 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996182 | CCGAGATTGCACCAC[G/T]GCACTCCAGGCTGGG | 11252 |
| rs554746512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907940 | AGAGTCTGAGAGAAA[C/T]CAGCCCGACTCAGAG | 11252 |
| rs554759407 | in-del | -/TGGGGTGGG | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962712 | TGCAGCCTGGATGCC[-/TGGGGTGGG]TGGAGGCATTGTGAG | 11252 |
| rs554779601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958870 | GTGATGGGTCACTTA[A/G]GTATCAGGATTTTAA | 11252 |
| rs554793373 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939839 | CCTCTAGTCATTTGC[C/T]TCTTCGCTAATTAAC | 11252 |
| rs554800892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901934 | TGGCCCTTCCTCTCC[A/G]TGGTGCAGAGGGAGC | 11252 |
| rs554825614 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984316 | TTCCTGCCCTCAATG[A/G]AAAGAAACAACTATA | 11252 |
| rs554835727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895924 | AGTCTCTATCGCCAT[A/C]AACCACCAGGGACAG | 11252 |
| rs554836206 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874157 | AATGCATTAAAAAAG[A/T]TTCCTATAGTGGGTG | 11252 |
| rs554841924 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964471 | GGGCACACAATAATT[A/G]GGTTGTTAATAGAAT | 11252 |
| rs554845849 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938403 | GGAATCCTCCCCTCT[A/G]GAACACACAGGAGGC | 11252 |
| rs554867184 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918144 | CATGACCCCATCCTG[A/G]GTAGGAACCAGCTGC | 11252 |
| rs554869830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908983 | CTTTTTATTTTTCCC[C/T]TATATCTACAGGGTT | 11252 |
| rs554874432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896501 | TCGATTGGGTAGTTA[C/T]ACCACTCTTTGGTTT | 11252 |
| rs554878984 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923480 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT | 11252 |
| rs554899334 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933133 | CCTAGTCTATTATTA[C/T]CTTTATGTGTCAGAG | 11252 |
| rs554904070 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015457 | TTTTGCGGTTTCGTC[C/G]GCATCCAGGGGTAAG | 11252 |
| rs554915047 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987011 | ATACTCCATTCCCAC[G/T]GACGCCTTCCCTAAC | 11252 |
| rs554920121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972184 | TCTTCTGCCTTGGGA[C/G]GCTGTTGATCTATGG | 11252 |
| rs554935836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009972 | CCTCCCGGGTTCTAG[C/T]GATTCTCCTGCCTCA | 11252 |
| rs554982144 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956223 | CACACATTTCAAATT[A/G]ATTCTAACTTCCTAT | 11252 |
| rs554984150 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972816 | ATGTTCCCGCCTCAG[A/C]CTCCTGTGTACCTGG | 11252 |
| rs554994729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967468 | CCAAAAGACAGGTAA[C/T]ACAACCCCAGAATCA | 11252 |
| rs554997040 | snp | G/T | 4.08589e-05 | 0.00451971 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891232 | GCCGGCCATGGTGGG[G/T]TCTGCTCTGCTCACA | 11252 |
| rs555012636 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935983 | CTTTGGGAGGCCGAG[C/G]TGGGTGAATCACAAG | 11252 |
| rs555018225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927797 | TCGCCATGTTGGTCA[C/G]GCTGGTCTCGAATTC | 11252 |
| rs555041015 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979397 | AGCGTGGTAGCAGGC[A/G]TCTGTAATCCCAGCT | 11252 |
| rs555053850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012210 | ATACATACAAACATA[C/G]AAAAACTAGCCAGGC | 11252 |
| rs555065281 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881178 | CTGTTAAGGGCCATA[A/G]AAGAAGTGCAGGAGT | 11252 |
| rs555076569 | in-del | -/GAGACTGC | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966351 | GCCTGGCGACAGAGT[-/GAGACTGC]ATCTAAAAAAAAAAA | 11252 |
| rs555077332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962752 | CCTGCCCCAAGTACC[C/T]AGTCACAAGAGCAAG | 11252 |
| rs555134003 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887371 | CACCTGCTGGATGGC[A/T]CGTGACTTAACCTCT | 11252 |
| rs555150481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916075 | GGCCAGCTGGGTGAC[C/T]GCAGAAAGCCATGTA | 11252 |
| rs555157345 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993966 | CCCAAGCCACAGTAT[C/G]TGTGGTTTGCTGCTG | 11252 |
| rs555170806 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911820 | AAGTTCACTGCCTTC[G/T]ATGATGGCTAAGGCA | 11252 |
| rs555184864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005510 | GCCCTGTAAGTGCCA[A/G]GATATGAGGGGAGTC | 11252 |
| rs555188437 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910283 | CCAGCAATGTCACTA[C/T]AGTTACAAAAAAGAG | 11252 |
| rs555235623 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976934 | GAAGTTTCTCCAGCC[A/G]ACACAATACCTCATG | 11252 |
| rs555242227 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952654 | TGAGCCACCACACCC[A/G]GCCTATTTATTTATT | 11252 |
| rs555272078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994391 | AGAAACCAGGCACAC[A/G]CATGAATCCAGAGCC | 11252 |
| rs555274538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918853 | TTTTTGACACACACA[C/T]GTCCTTAACCATAAA | 11252 |
| rs555274623 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003880 | GGTGGGTGTACCAGC[A/G]AGTCACCCACGGCCT | 11252 |
| rs555299856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946096 | CCTCTGAACAAATGC[A/G]CAAATGAATTAGAGG | 11252 |
| rs555312129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946697 | TCACACAGGCATGCG[A/C]ACACACATGATCCTC | 11252 |
| rs555339332 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912133 | TCAGGGGTCAACTTC[A/G]AACGCTCAAAATCTG | 11252 |
| rs555339750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906112 | TGGCAGTCACTTGTG[C/G]AACTGTCTTGTGCTG | 11252 |
| rs555392525 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870737 | GAAACCCGACCATAA[C/T]CCGGTCCCACCTTCC | 11252 |
| rs555413810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012738 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA | 11252 |
| rs555420680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923620 | TTTTAGTAGAGACGG[C/G]GTTTCACCGTGTCAG | 11252 |
| rs555420738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930840 | GGGGCAGAGCTTGGA[G/T]TCAAACCCAGACCAG | 11252 |
| rs555442176 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881021 | CGCTTCCAGTCAGGA[C/T]GGCTCTGGCCCTCCA | 11252 |
| rs555497127 | snp | G/T | 6.81222e-05 | 0.00583579 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876095 | CCCACAGCCTGCAGG[G/T]TGGAAGCCCTCCTCC | 11252 |
| rs555514083 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944084 | TCCTGGCCACATCAG[C/T]AGTGAAAAGTCCACA | 11252 |
| rs555530102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918056 | AGAATCGTGGTGAGG[A/G]TCAACTGAGAAGGAT | 11252 |
| rs555542144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911541 | GAGGGCCACTCATGG[G/T]TACAGACTGGCGGCA | 11252 |
| rs555557576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925824 | TGTCTACCACCGGCC[C/T]CACGGGAGGCCCTCC | 11252 |
| rs555592739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895118 | CCCTCCAAAGACCTC[C/T]CCCAGCAAGGCTGGC | 11252 |
| rs555614045 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994196 | AATGACAGTGCAGTG[C/T]GCTCCTGCTCAAGTG | 11252 |
| rs555635687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931962 | AGAACAGAAAACCTA[A/T]CCTCACTTCCAGTTT | 11252 |
| rs555637409 | in-del | -/TCAATGAAAAGAAACAACTATATAA | 0.00517822 | 0.0506191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984309 | AAATTCTTCCTGCCC[-/TCAATGAAAAGAAACAACTATATAA]TCAATGAAAAGAAAC | 11252 |
| rs555687755 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013942 | GGCCACCTTCCCTCA[C/G]GCACCCAAGCCAAGA | 11252 |
| rs555699487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948526 | ATCTATAGTCCCAGA[C/T]ACTTGGGAAGCTGAG | 11252 |
| rs555733347 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889318 | CAGCATGAGAGAGAG[G/T]ACCATACTAGGGGGC | 11252 |
| rs555759505 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929664 | GACATCTTTCCAATT[C/G]TGTGACGTCTGCTCC | 11252 |
| rs555781989 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872909 | TCTTTCCACCGCTTC[A/G]TGCCTCGGGCCCCTG | 11252 |
| rs555804538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894521 | GCTGGGATTACAGGC[A/G]TGAGGCACCGCGCCC | 11252 |
| rs555823399 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887254 | CTGAGTGACGAACTC[C/T]CGTGTAGATGACGTG | 11252 |
| rs555841912 | snp | C/T | 9.96049e-05 | 0.00705638 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888614 | TGACACGGTGACACT[C/T]GACGTGTAAAAACAA | 11252 |
| rs555861302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973844 | GGGGCACAGCATATG[C/T]TAAAAGAGGAAAAGA | 11252 |
| rs555895592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934591 | GCCACCTGAGACTGC[C/T]GCCTTGCTGGTCAAC | 11252 |
| rs555905347 | in-del | -/CG | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884288 | AGACCTCCTGATGAA[-/CG]CGCCATCCCAAACCT | 11252 |
| rs555948694 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901305 | CAAATATGCCAAGAA[A/G]CTCTAGCATCTCCTC | 11252 |
| rs555952718 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928698 | GGAATCACTGGGTAT[A/T]CCCTACCTGGAACAC | 11252 |
| rs555961867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939696 | TTCTTGTGCCCGCTC[C/T]GGCTTTTACAGTCTG | 11252 |
| rs555973451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974565 | CCAGCCATGGCCAAC[A/G]TGGTGAAACCCTGCC | 11252 |
| rs555992471 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887655 | GACCAAAGGAGGGGA[G/T]GTGGGGCCGAGGGCT | 11252 |
| rs555996378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891426 | TATTTTTGGGATGGA[A/G]TTTCGCTCTTATTGT | 11252 |
| rs555999251 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008472 | GCCAGGCTGGTCTCA[A/C]ACTCCTGACCTTGTG | 11252 |
| rs556011668 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017186 | CCTCTCCCAAATTTT[G/T]GGGGGTTTTTGTTTT | 11252 |
| rs556036932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968650 | GCACATTAGTGTGAG[A/T]GGATGAGGTGGGGAA | 11252 |
| rs556038929 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972866 | GCACCCAGCTCAACC[A/G]TGCTTTTAAATGGCT | 11252 |
| rs556047486 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956505 | AATGTCATTCATTCA[C/T]TCATTCATTCAAATC | 11252 |
| rs556049202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969433 | TTACCCTGTTATTAG[C/T]AGTACCACTTAACAC | 11252 |
| rs556068200 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016827 | ATCTGGGTAAGTTCC[A/G]CTTACATCGCAATTC | 11252 |
| rs556077925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882345 | TTTAGAAGGCAGGGG[A/C]CAGCTACCCTTTGTC | 11252 |
| rs556116601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883229 | CAGCAGAGCAGCCTC[A/G]GGCAAGTCATTTAAT | 11252 |
| rs556145700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965399 | TGCATTCAATTGTAT[A/G]TAAACTAATACCTCA | 11252 |
| rs556151359 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999544 | CGTGGTGGTACATGC[A/C]TGTAATCCCAGCTAC | 11252 |
| rs556156049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011112 | GAACCACCACTGGGA[C/T]GCATCTGGAGTCTGT | 11252 |
| rs556203971 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946658 | ACTGATGCAGTGTTA[C/T]TCCAACATAATCTTA | 11252 |
| rs556209133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959438 | AAACATGCCAAAGCA[A/C]AGGTGCAAAGTTATT | 11252 |
| rs556210963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922353 | ATTCCACAACCAGAC[A/G]AAAGAACAGGTCATT | 11252 |
| rs556227973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953322 | AATGCAATGGAAAAT[A/G]GGCATGATGAAATGC | 11252 |
| rs556238520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947458 | ACAAAAGAGGAGCGG[C/T]CTCTTCCCATGCTTG | 11252 |
| rs556259252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976777 | TTCGTCCTTCCATCA[A/G]CCCTATACAGCAGTA | 11252 |
| rs556267667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940256 | GGATGTCATTTTACA[A/C]CAAAAATAGATTTTT | 11252 |
| rs556272660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916332 | GCACCACAAAGAAAA[C/T]CCAACTGATTGTACA | 11252 |
| rs556286187 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983761 | CCATCATGCCTATCA[-/T]TTTTTTTTACATCCC | 11252 |
| rs556349793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892063 | AGAGGAGGAAGCAGG[A/G]GCCTGCTCTGGACCA | 11252 |
| rs556444537 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007611 | TGGCACAATCCCTCC[C/G]AAGTCACTTCCCTGA | 11252 |
| rs556445418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941078 | ATCCTGGCAATCACT[A/G]ATCTACTTTCTGTCT | 11252 |
| rs556456948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971755 | GCCCCGTCCGGGAGG[C/T]GGGGGGTAGCCCCCG | 11252 |
| rs556462975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885077 | CTCTTGTCTTTCAGC[C/T]CACTCCATCCCCCTC | 11252 |
| rs556509189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922821 | GCTGACATCCTACTA[G/T]GGCAGATTGGCACAC | 11252 |
| rs556515163 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884152 | GGCCAGCAATTGGCC[A/G]GGTCAACCAGGCCTT | 11252 |
| rs556523506 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916865 | TAGCCATTGTTCTTA[C/G]AATCACCACAGCAAG | 11252 |
| rs556552819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005672 | GGCACTTTAAAGGTA[C/T]AGTTTGCTGGCAAAT | 11252 |
| rs556569190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920951 | AGAACCACAGGCATG[C/T]GCCCAGCTAATTTTT | 11252 |
| rs556629142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956044 | TTACATCAACATTTC[A/G]TCAAGTAAGCATTTT | 11252 |
| rs556636480 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880146 | TGTGGCTGAGTCCAC[A/G/T]GCTCTGCTCACACGT | 11252 |
| rs556653340 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939844 | AGTCATTTGCTTCTT[C/T]GCTAATTAACACATC | 11252 |
| rs556704854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950853 | CCGGGATGGGTAGAA[A/G]TGACAAGGCCCCTGT | 11252 |
| rs556716456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962548 | TGGAAAAGGAGAAGA[A/G]GCCCAAGGCAGAACT | 11252 |
| rs556721712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986787 | GGGGCAGCAGCTACT[A/G]CATCAACACTTGTCT | 11252 |
| rs556726047 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999256 | CTCCTGTAAGTGGTT[A/T]AAGCAAACCAGCCAC | 11252 |
| rs556735152 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980402 | GAGGTCAAGGCTGCA[C/T]GATCACACCACGACA | 11252 |
| rs556757339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877105 | CTCAAGAGACAAATC[A/G]GCTCCTCCTGTGACC | 11252 |
| rs556771374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910671 | TGTCACTCTTGCTGT[A/C]TTAAGTGAAATATTT | 11252 |
| rs556785761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993388 | GGCTTAACAGTGTAT[C/T]CATATGCCAAAACTT | 11252 |
| rs556791028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899549 | TGGGAAAGGCCAAGT[A/G]TGGGCAGAGGTGGGT | 11252 |
| rs556791669 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930086 | GTGTTAAATATGAAT[A/G]CCATGCTTTTCTCAT | 11252 |
| rs556794189 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871305 | CCCACGTGGCTGGCT[A/G]AGGCTCCTGGGCCCG | 11252 |
| rs556832419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904730 | CAGCCCCCCCATACT[G/T]CACTCCAGTCTACCT | 11252 |
| rs556886311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990034 | CACATATGTATATAT[A/G]TGTATATATATATAT | 11252 |
| rs556890959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947691 | GGGGGGGGGGACCTC[C/T]TAATGATCCAGCTGC | 11252 |
| rs556904022 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906086 | CAGTGCTGAAAACTG[C/T]CCAAGGGAAATGGCA | 11252 |
| rs556926987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901890 | GCGTCTTCCTTCCGT[C/G]GTTCAGCTCGGACCA | 11252 |
| rs556953906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944530 | AACAGTTACCAACCT[C/T]TGACCCTTAAGTCCC | 11252 |
| rs556960615 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876710 | CCCCGAGGAATGGGG[A/G]TGCCAGAGAGCCTGT | 11252 |
| rs556964152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890011 | CAAAGGGACTTTTTT[A/T]TTTTTTTTTGAGACA | 11252 |
| rs556976819 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945638 | CCCCCTCACCACTAC[A/C]ACATTCAATCAGCTT | 11252 |
| rs556984811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975976 | GCCAATGCTGAGACA[C/T]CCTGGCCCCCATGGC | 11252 |
| rs556999154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890691 | CTGCACTCCAGCCTG[G/T]GAGAGAGAGTGAGAC | 11252 |
| rs557003056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883431 | CTTGACCCGTGACGC[A/G]TCCCTACACGGTTCT | 11252 |
| rs557004002 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909924 | ACTCCCTCAGCTCCC[A/G]TGTCAGAGGGAAGGG | 11252 |
| rs557015876 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001812 | CATGGTGGAGGCATC[A/C/G]CAGGAATTCTAGGGA | 11252 |
| rs557016936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938304 | CACGGTTCTGAAGAT[C/T]CCACAGAAAGATATG | 11252 |
| rs557040151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883871 | TAGCTGGGTGTGGTG[A/G]CGCATGCCTGTAATC | 11252 |
| rs557051473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995138 | ACTGGACACTGCAAC[A/G]TTTAACTCACATTGA | 11252 |
| rs557051685 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924842 | GATCACTGCAAGCTC[C/T]GCCTCCCGGGTACAC | 11252 |
| rs557057954 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956423 | CTGTGACATGCAAAT[A/G]CATTTAGACCACCTA | 11252 |
| rs557087208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003364 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAG | 11252 |
| rs557115124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989586 | TGGATCACGAGGTCA[C/T]GAGTTCAAGACCAGC | 11252 |
| rs557126415 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883153 | AGACAAGCATCCACA[C/T]GATGGGAGTCACTCC | 11252 |
| rs557130408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912706 | GGCAAGGGTAAAGGC[A/G]GCAATTATTTCCCCT | 11252 |
| rs557145201 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015390 | GCGCAGATTACTCTC[C/T]CAAAGCCGCTCGCTG | 11252 |
| rs557150653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004194 | TGATGGTGACCCTCT[A/G]AAGGCCACTGAATCT | 11252 |
| rs557169181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906934 | CTTACAACCATCCTG[G/T]AAGTAGGAAATGAGC | 11252 |
| rs557182095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009939 | CAGTGGCACAATCTC[A/G]GCTCACTGCAGCCTC | 11252 |
| rs557191810 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913444 | AGATCGTGCCATTGC[A/C]CTCCAGCCTGGGCAA | 11252 |
| rs557195439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908018 | AATGTTGAGAGTCAC[A/G]TGCCAACTCTTCAGG | 11252 |
| rs557196479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964041 | GACATTTTCATTACC[C/T]CAAAGAGAAACCCTG | 11252 |
| rs557205297 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998738 | GGCCCTAAATGAGAA[C/T]AAGCATTCCTGTTTT | 11252 |
| rs557206272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907512 | TAATTAAGCTGATGC[A/G]CACCCTGTCCCGAGG | 11252 |
| rs557237499 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995890 | GCAACACAGTGAGAC[C/G]TGCCCCCTTCCCCAG | 11252 |
| rs557272252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914289 | CCGGGCTGGAGTGCA[C/G]TAGTGCAATCTCAGC | 11252 |
| rs557276584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938692 | CCGGTGTGTGCTACC[C/T]GTGCCTGGCTGGTGA | 11252 |
| rs557290432 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921752 | AAGCTTTTTTTTTTT[C/T]TTAGACAGAATCTTG | 11252 |
| rs557306949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43015005 | GCGGCGACCCCTGAC[C/T]TCGGCGGCCACTCAC | 11252 |
| rs557312030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978147 | TGCACTTTTTTCAAT[A/T]ATTTGTTATCAAAAG | 11252 |
| rs557315441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878640 | TGCACACAATACAGA[G/T]TGAGCATGAACCTCG | 11252 |
| rs557343290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932894 | TAGAAGTCCACACTT[C/T]CCACACTTTTATTTT | 11252 |
| rs557348345 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968938 | ACTGAGCCCCACTAC[C/G]GGCATCCCAGAGTCT | 11252 |
| rs557377168 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976550 | GCTTGCTGCTGGGTG[C/T]TGGCACCTATTTCTG | 11252 |
| rs557400218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893188 | GTTCTGAGTTAACTC[A/G]GCAAGTGCAAGTGTG | 11252 |
| rs557400258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011821 | GTTCCAGATCAGCCT[A/G]GCCAACATGGTAAAA | 11252 |
| rs557437026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886700 | GCTGGATTTTGGAAA[C/T]TGCGTCAAGAAGGGT | 11252 |
| rs557489291 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967322 | AGATCCCAATGTTAC[C/T]GATCAGGGCTTTTTC | 11252 |
| rs557496943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899446 | CAGGCAGAGCACACA[C/G]AGACACCTCTGTATG | 11252 |
| rs557500523 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001588 | GGCACAAAAACCTGC[C/T]TGTGCTTGGGAAGCA | 11252 |
| rs557502248 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995467 | AGGAGACAAGGTTTT[C/T]AAAGCAACTTTTCAG | 11252 |
| rs557525881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010526 | CCATCCTGGCTAACA[C/T]AGTGAAACCCCGTCT | 11252 |
| rs557527403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966134 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCGGA | 11252 |
| rs557535011 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955692 | TGCCACTTTCCTTCA[C/T]GGCTTTACAGTCTTG | 11252 |
| rs557568384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964397 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 11252 |
| rs557580661 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993291 | GAGCAGTGGTGGCCT[A/G]GAAGAAGTGGGGGCA | 11252 |
| rs557590336 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930419 | TTCTCTGGACCCTCC[C/T]GTCCTCGTGTCTCAC | 11252 |
| rs557614406 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003420 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 11252 |
| rs557651977 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873161 | TGCAAATGTGAACTG[A/G]TGATTAGAAGGTTCA | 11252 |
| rs557677123 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951573 | TCCTGCATCCCCCGG[C/T]TGGGCTCCTCCAGGA | 11252 |
| rs557686615 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999368 | GTGTGTGTACGGAGG[A/C]ATTAAAAAATCTGTC | 11252 |
| rs557692564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923999 | GTGAGTTACGATTGT[A/G]CCACTGCACTTCAAT | 11252 |
| rs557758853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935049 | GCCTCCTGAGTAGCT[A/G]GGACTACAGGTGCCC | 11252 |
| rs557782959 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875986 | CCAATTGGCTGCTTT[A/T]GACAATGAAGCCAGG | 11252 |
| rs557817788 | snp | A/G | 3.45453e-05 | 0.00415589 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879016 | CCCCACCATGGAACG[A/G]CCTCTTTTGGATGGA | 11252 |
| rs557869473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935395 | CTCCTGCACAGACTG[C/T]CCCTCTTCCACATGT | 11252 |
| rs557884183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936712 | GATGAGGGGTTCAAG[A/C]CCAGCCTGGCCAACA | 11252 |
| rs557946228 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887482 | AACCAGCTTAGGCCT[A/C]TTGCCTCCCCTCTGC | 11252 |
| rs557951414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949157 | TTTCTTAAATAATAG[A/G]TGCACATTTTAACTT | 11252 |
| rs557971167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880596 | TGGCACTCTATGAGG[A/T]AGCCGAACGCAGACA | 11252 |
| rs558007878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875456 | TTCATTGCAACCTCA[A/G]TCTACTGGGCTCAGG | 11252 |
| rs558010608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942933 | TTAGAATTGGCTTGT[G/T]GCTTTGGGATTTTGA | 11252 |
| rs558058772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900878 | AAACATCCCTCAGGC[C/T]GGGATCAGAGCTGGT | 11252 |
| rs558076288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953928 | TGCTTAGAGCAAGAA[C/T]GGTATTCTGGAGAGA | 11252 |
| rs558076951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931918 | AATGAAAACGTTTAA[C/T]GTTTTCCCATGGAAA | 11252 |
| rs558088661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954663 | ACAGTCACGTGGTTA[C/G]TGGCTACCACACTGG | 11252 |
| rs558093960 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894407 | GCCATCACACCCAGC[C/T]AGTTTTTGTATTTTT | 11252 |
| rs558098915 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869907 | TGCTGGTAAGTTCTC[A/G]GGACAGACACAGACA | 11252 |
| rs558126942 | snp | A/G | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993895 | CAAAAGGTTCCTGAA[A/G]CACTCCTATGCAGCT | 11252 |
| rs558139438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987734 | GACAGGGTTTAATCA[C/G]TGTGTTAGCCAGGAT | 11252 |
| rs558173302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013982 | CCAGGTCCTGTTATA[C/T]GTCAAAGGCTGCAGC | 11252 |
| rs558191845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948263 | TGAAGATCAGACACC[A/T]GCTCAAGTCACTAGT | 11252 |
| rs558258067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979647 | AGATACCTCCTTCTC[C/T]ATGAATTCTCTGGCT | 11252 |
| rs558265404 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996732 | TAGAGACGGTCCAGG[A/C]CAAAATGGACACACT | 11252 |
| rs558283998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907976 | TGCAACAACCTACAG[A/G]GAGCGCCTTCCTGGC | 11252 |
| rs558339612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970624 | AATACAAAAGTTTAA[A/C]GAACATTCATTACGT | 11252 |
| rs558363545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945272 | CTTTGGGGAGGGAGC[C/T]GACACTCACCAGCTC | 11252 |
| rs558412824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934239 | CATACTAAATTCAAA[A/G]CATATAACCGAGGCC | 11252 |
| rs558434019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881866 | GTCAGGGACCTGAGG[C/T]CCTGTGTGCCTACGG | 11252 |
| rs558445867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964634 | GGCAGCCTGGCACAG[A/G]GCAGGCTCTACAGTT | 11252 |
| rs558453189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888504 | CACCTGTGGCCTTCT[C/T]GAGGACAGGGGTGTG | 11252 |
| rs558456539 | in-del | -/ACAAGTTTCAACAAGT | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969971 | GTTTCAACAAGTATC[-/ACAAGTTTCAACAAGT]AACACATGGCCAATC | 11252 |
| rs558491551 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905787 | GTGCTCCTGGTGGGT[A/G]GATGGGTAAAAGGGA | 11252 |
| rs558495182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889201 | GAACACGCACATGGA[A/G]CACGCACATGGAACA | 11252 |
| rs558504851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907686 | ACATTCGCTCGCTTC[A/G]TGCTTGCGCTCAGGG | 11252 |
| rs558516449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976671 | ACATGGGTTTTCTTT[G/T]TAATGTGATACAGTG | 11252 |
| rs558529176 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002367 | ACAACCTTGGGAACG[C/T]GGAACATTAGCTCCA | 11252 |
| rs558531219 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970881 | AGGCTGGCCTGCAGC[A/G/T]CCTCCCCACGCCACC | 11252 |
| rs558539136 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016181 | CCAGTTCTCTAAAAA[A/G]TAAAATAAAAGAAAA | 11252 |
| rs558560909 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965120 | AGGAATGAGCTACTG[A/T]CAGATGTGACATGGA | 11252 |
| rs558560921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958929 | CAATAAAGGGGAGCC[A/G]CTGTTTTTCAAAAAT | 11252 |
| rs558597753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990798 | TTGCCAATAAGAACA[C/T]GAAGATGTGGAAGAG | 11252 |
| rs558620584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959315 | AGCATGTAATAAACA[C/T]TAACGCCTTAAAGTA | 11252 |
| rs558629118 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945905 | ACTCAAACTCCTCCC[A/C]CTACTTCCTCCCGAA | 11252 |
| rs558645007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959818 | TTCTGTCAGATGCCG[G/T]CTAACTCTGCAGCTC | 11252 |
| rs558658693 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991412 | GAGCCCCACCCCACC[C/T]ATCCAGGCACAGAAG | 11252 |
| rs558662183 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982608 | AAACATGTGCTGTGT[-/C]CACTCAGGGTTAAAT | 11252 |
| rs558667122 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996203 | CCAGGCTGGGCGACA[G/T]AGCGAGACTCCGTCT | 11252 |
| rs558686159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874830 | CACCTCACTATTTCT[A/G]AGTCTTGGCATTGGG | 11252 |
| rs558697334 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011954 | AATCGAGACCATACT[C/G]GCCAACACGGTGAAA | 11252 |
| rs558721179 | snp | G/T | 1.68587e-05 | 0.00290329 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879205 | GAGAGAAACCAAAGG[G/T]TCACTACTTGCTGGA | 11252 |
| rs558733931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986033 | AGGTCAGGAGGCTCA[C/T]GCTTGACTTTCCAAA | 11252 |
| rs558788805 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952675 | TTTATTTATTTTTTT[A/T]TTTTTGAGATGGAGT | 11252 |
| rs558799542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986393 | CAAGGGCAGCATTCA[A/T]CCGGCCAAACGAAAT | 11252 |
| rs558808921 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966353 | CTGGCGACAGAGTGA[C/G]ACTGCATCTAAAAAA | 11252 |
| rs558834328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971284 | TGGAGACGGGGTTTC[A/G]CCGTGTTGGCCGGGC | 11252 |
| rs558852897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946743 | GATCAGGACTTCAGA[A/G]CACATGAGGACGCGT | 11252 |
| rs558856351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976801 | AGCAGTATTGTAATT[C/G]TCCTGCCAATTTTAT | 11252 |
| rs558878761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992327 | TGGTGATGCGCGCAA[A/T]GCACTTTGGAAAAGT | 11252 |
| rs558894065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891782 | AGTCTTAATTTACTT[A/G]AAGGTGGCCAGAGAA | 11252 |
| rs558895927 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010656 | CGCAGCCTGCAGTGA[A/G]CCAAGATCACACCAC | 11252 |
| rs558898019 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922922 | TGGGGGTGGGGCGGG[C/T]TTACTGAGATAGAAT | 11252 |
| rs558900986 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903816 | GTCCTTTCCTCGGGG[A/C/T]CTCAATTCTGTCTCA | 11252 |
| rs558903877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960744 | GGTGCCAGGAGGGTT[C/T]TGGAGCTGTGCTGTG | 11252 |
| rs558933533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922275 | TGGGCTTGATAACAG[A/G]TATCAGGTAAACAAA | 11252 |
| rs558950329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004437 | TGCAGGAGCAAAGGT[C/T]GCAATTGCTTAATTA | 11252 |
| rs558971125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875594 | AGCCTGGGGTACAGT[A/G]GTGTGACCTTGGCTC | 11252 |
| rs558982504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011079 | AATTCTGCAGAAATT[C/G]CTACAAAACTATCCC | 11252 |
| rs558987131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879739 | CCATGTGGAAAGGCA[A/G]GTGCAAATAAAACCA | 11252 |
| rs559010266 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870040 | CCCACGTTCCCCCCA[C/T]CCCCGCCGGCCCGCG | 11252 |
| rs559013130 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005060 | TACTTAAACATTAAT[A/C]TAAAAGTAAAAGGGC | 11252 |
| rs559014946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915308 | AGGGCATCAGACAGG[A/G]CATATGCTCTTAGCT | 11252 |
| rs559029441 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940928 | ACACAGTTCACCCAT[C/T]TAAAATGTACACAAT | 11252 |
| rs559059775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994058 | AGTGAGCTAAAGCCG[A/G]AATCAAATATGAGCT | 11252 |
| rs559059876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987298 | ACTGATCATCACTGT[C/T]ATTATATGGGCTGCT | 11252 |
| rs559066404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913225 | TGGCTCATGCCTGTA[A/C]TCCCAGCACTTTGGG | 11252 |
| rs559102726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885890 | GAGCTCCACAGCGCT[C/G]TGGCTATTCCCCTAT | 11252 |
| rs559104583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998706 | GGTGAGAGCCCCACC[A/C]TCAAGCCTGGACCCA | 11252 |
| rs559116952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992928 | TAGCACTCTGGGAGG[A/C]TGAGGCGGGCAGATT | 11252 |
| rs559130289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916170 | AAGGTCTCAGTACCC[C/T]CAGGTCACAGGCCGT | 11252 |
| rs559141846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954960 | CAGCCACAACAAGCT[C/T]CTAAGTCTGGCAGAT | 11252 |
| rs559159102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904223 | CTGCTCCCTTGGTGC[A/G]TGTTACACAGATGTC | 11252 |
| rs559166497 | in-del | -/TT | 0.446118 | 0.155041 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962183 | AGGATACCAGAAAAC[-/TT]TTTTTTTTTTTTTGT | 11252 |
| rs559178916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894151 | CCTAGTAGGAATAAG[C/T]GTCCCCATTTTACAG | 11252 |
| rs559192445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909685 | AATTTAACAGGGAGC[A/C]TAAGAGCTTAATTAC | 11252 |
| rs559193208 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982125 | GTCCGGGAGGGAGGT[C/G]GGGGGACAGCCCCCC | 11252 |
| rs559198923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947313 | AGACAAAGAGTATTA[C/T]TGACAACATGCATGA | 11252 |
| rs559265461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013015 | CAGGCTGGTCTCTAA[C/G]TTCTGACCTCAGGTG | 11252 |
| rs559272330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940392 | GGTCAGCATGTGTTT[C/G]CTGAATGAGTAACAC | 11252 |
| rs559278341 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002929 | ATAATACAATTATAA[A/C]AATGTCAGTTATTGA | 11252 |
| rs559299927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013600 | GCATTCAACACTGCC[C/T]GCCTGGTCGGTTCCC | 11252 |
| rs559302048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940971 | GTTCACAGAGTTGTG[C/T]CACATCATGACAATC | 11252 |
| rs559321224 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911109 | TGGGGTTTCACCATG[G/T]TGGCCAGGCTGGTCT | 11252 |
| rs559343841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954203 | GGGAGGCGGAGGTTG[C/T]AGTGAGCCGAGATCA | 11252 |
| rs559350711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917682 | GCCGTGATGAACTAC[C/T]GCTATAGTCCTATTT | 11252 |
| rs559359198 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944037 | AGGAATGCTCACTAA[A/G]TTCTACCTGCTAAGC | 11252 |
| rs559375758 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993820 | CCATGTGCGCTGTGG[C/G]ACCCAGACATCACTT | 11252 |
| rs559396498 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971373 | ACTGCAGACGGAGTC[C/T]CGCTCACTCAGTGCT | 11252 |
| rs559398130 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935017 | ACCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 11252 |
| rs559424844 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008541 | GGCGTTAGCCACCAC[A/G/T]CCCGGCCTAAGTTCA | 11252 |
| rs559440528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905140 | ATCTTCAGAAGACAA[A/G]CTTCTTGACAGCACA | 11252 |
| rs559450087 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006236 | ATCTCAGACTTGCAG[C/G]CTACAGAACTGTAAG | 11252 |
| rs559472675 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946513 | TGAGATCGCACCACT[A/G]CACTCCAGCCTGGGG | 11252 |
| rs559481625 | in-del | -/CACACACACACCACCCCCCCCCC | 0.114387 | 0.210022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014355 | ACACACACACACAGA[-/CACACACACACCACCCCCCCCCC]CCCGGGACACGGAGG | 11252 |
| rs559481893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919813 | GAAAGAAAGAAAGAA[A/G]AAGAAAAAGAAACTG | 11252 |
| rs559483991 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937959 | CGGTAGAAGTCTCAC[C/T]TGCGCCTGCCTGGTT | 11252 |
| rs559498623 | in-del | -/TGAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908374 | CCAGAGCCTACTGAA[-/TGAA]GGTAAGGGAGGCCAG | 11252 |
| rs559514343 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015374 | ATGGGCTGCGAGGGT[A/G]GCGCAGATTACTCTC | 11252 |
| rs559525265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988313 | CCACGAGGACACAGA[C/T]AGCTGTGGGATGTGT | 11252 |
| rs559525771 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941687 | GGCCATTTGTATACT[A/G]TCTTTGAAGAAACGT | 11252 |
| rs559552832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881966 | GAGAGGACATAACCG[C/T]GACTTCAGGAGAGGT | 11252 |
| rs559567727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973352 | ATTTCCACTTGCTCA[A/G]GAATTGACGAGCAAA | 11252 |
| rs559609369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931173 | CACAGTTGTATCCCA[C/T]GGCTGGGCACAGCAC | 11252 |
| rs559624197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944214 | GGACTCTGTGGAACC[A/G]CACCCCCAGCCATCC | 11252 |
| rs559682325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936210 | GGCAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 11252 |
| rs559688887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927572 | TTATTTATTTATTTA[G/T]TTAGTTATTTAGTTA | 11252 |
| rs559691679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887929 | TTCTGCCACCCCTGG[C/T]TCCACAGCCTCTGCC | 11252 |
| rs559692801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936970 | ACCTATTTACACCCA[C/T]TGCGAATGCATTAGT | 11252 |
| rs559697161 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016332 | CTCTGTGGCATTGTC[A/C]TTATGACAATAATTG | 11252 |
| rs559741855 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888243 | AACCCTCCATACCAG[C/T]TCACACCACACCCAT | 11252 |
| rs559768565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967663 | GGAGGCCGAGGCGGG[A/C]GGATCACGAGGTCAG | 11252 |
| rs559808547 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985789 | GATAAGTCTCCCAGA[C/T]GCCTAACCCCTCCCC | 11252 |
| rs559816802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011229 | TGCCTTCGTAACTAA[A/G]GCATTGCTGCACTGC | 11252 |
| rs559829619 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968114 | CAGCAATGGTAGCGC[G/T]GGAAGCTGCAACCCT | 11252 |
| rs559842594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001531 | CAGGAAGCTGGGCAG[C/T]GCCTGGCAGAGCCAG | 11252 |
| rs559843666 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962215 | CCAGAGCCCCACTTA[A/C/G]GGCTGCTGGTTATGG | 11252 |
| rs559874140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915672 | GAGATTATATACATC[C/T]TTATTAATTTAAGTA | 11252 |
| rs559874270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922493 | TCTAATCCTCTAACT[A/G]CAGAGGTAGGCAGAG | 11252 |
| rs559889047 | snp | A/G | 1.65825e-05 | 0.00287941 | missense | PACSIN2 | GRCh38.p7 | 22:42890985 | GCTTCTGTGCCTTCC[A/G]AAAGCCGTCCTCAGC | 11252 |
| rs559889423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876833 | CCTGGACAGAGAGAG[A/G]GGAAGAGAGACAGAG | 11252 |
| rs559890283 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924244 | TCTCTCCACTGTCAG[C/T]GCCACTATCACCTCT | 11252 |
| rs559927728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884163 | GGCCGGGTCAACCAG[A/G]CCTTCCAGAGGTCCA | 11252 |
| rs559935310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916415 | GGTGGGGGTGGGGAT[A/G]GGGGGTGGGGAAGGG | 11252 |
| rs559973489 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938682 | CAGTGGCATTCCGGT[A/G]TGTGCTACCCGTGCC | 11252 |
| rs560028187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877409 | GTCTCCTCTGAGAGT[G/T]ACAGTGTGGGAGGGG | 11252 |
| rs560029933 | snp | A/C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885841 | CCAGGAAAAGGCCAC[A/C/T]CCTGCCAGGGCTGGG | 11252 |
| rs560037257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004591 | CCTCTGAAGACCACA[A/G]TTCATGATCTTGGCA | 11252 |
| rs560037830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946891 | CTGGGCCGTGGGTCC[A/G]GGTACCTGCGCTTCC | 11252 |
| rs560049360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997839 | TGAGCTGAGATCACA[C/T]CACTGCACCCCAGCC | 11252 |
| rs560069318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959113 | GGATGAGAAATGAGA[A/C]GAACTGAGGGGGAGG | 11252 |
| rs560085653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976861 | AACTAATTTGGCTAA[C/T]GTCAGAGAATTAGTA | 11252 |
| rs560128458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891468 | TGCAGAGACGTGATC[C/T]TGGCTCACTGCAAAC | 11252 |
| rs560133223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952515 | AGGCGCGCACCACCA[C/T]GCCTGGCTAATTTGT | 11252 |
| rs560146289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940551 | CCAGAAGCAGTGCCA[C/G]CAGAATATGAGCCCC | 11252 |
| rs560202002 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913182 | CGCTTGCCTTATCTG[C/G]AAAAAAGAGACAATA | 11252 |
| rs560209100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941245 | CCTTTTTGTTGCTAA[C/G]TAATATTCCACTGTA | 11252 |
| rs560258485 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007101 | AAGATCTTCATCCCG[G/T]TATTTTAAATACCCA | 11252 |
| rs560297604 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992349 | TGGAAAAGTTTGGCA[C/G]TGTCTGGACATGTTA | 11252 |
| rs560320442 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998272 | CGTGAATATAGGAAC[C/G]TTCTTTGCTGCTGCA | 11252 |
| rs560354698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952750 | TCACTACAATCTCTG[C/T]CTCCCAGGTTCAAGC | 11252 |
| rs560359525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966334 | CGTGCCCCTGCACTC[C/T]GGCCTGGCGACAGAG | 11252 |
| rs560368096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965509 | AGTCTAGTAACAGAG[C/T]TTCCTTCCTACCCAG | 11252 |
| rs560371665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960426 | ACAGAGTCCCCTGGA[A/G]ACAGGCAGGTGACCC | 11252 |
| rs560377091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934947 | TTGAGACAGAGTTTC[A/G]CTTTATCGCCCAGGC | 11252 |
| rs560414872 | snp | C/G | 0.00160353 | 0.02827 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875139 | ACAGGCGTGAGCCAC[C/G]ATGCCCAGCCTACTT | 11252 |
| rs560437676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879963 | CCTCACGAGTTCTCG[A/G]GTGGCGAACTGGCTT | 11252 |
| rs560462525 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874505 | CATGGTAGGTGTGGG[A/C]AGGTAGGTGTGCACA | 11252 |
| rs560491789 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977454 | TCAGGAAAACACAAA[G/T]TAAAATAAAAGTGCT | 11252 |
| rs560494969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898647 | GGGGCCACATCCCTC[A/G]CAATCAAGCTCTGCC | 11252 |
| rs560518064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903945 | ACTACCCTGAAAGCA[C/G]CCCTTGCCGTTTGAT | 11252 |
| rs560526582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899027 | GCCTTTCACAAGGAC[A/G]CTGGAGAAGGTCTGC | 11252 |
| rs560587239 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943360 | TTTACCTTTTCCTTT[A/C]CAATCTGTATGCCTT | 11252 |
| rs560595107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886936 | TGTCAAACATGAAAG[C/G]CCTCTTCCTCTCCAT | 11252 |
| rs560605132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930339 | AGCCACAACATGCAG[A/C]AGCACCAGGACCTCT | 11252 |
| rs560606236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978338 | CCACCTAGCTGTTTA[C/T]ACATCTTCTGTTTCT | 11252 |
| rs560614383 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956966 | AAAAGGAAGCCGATT[A/G]GAATATTCTATACTT | 11252 |
| rs560624664 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888280 | CCACCACTGGCCACA[A/C]CCATTCACACCTGCC | 11252 |
| rs560631557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880722 | GCACAGGGGCTGGTT[C/T]CCAGCCCATGGACCC | 11252 |
| rs560637344 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989757 | AGTGAGCTGAGATCG[C/T]GCCACCGCATTCCAG | 11252 |
| rs560648179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011974 | ACACGGTGAAATCCC[A/G]TCTCTACTATAAATA | 11252 |
| rs560660118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892957 | TAAAGCTACAGAATC[G/T]TCTGAGCTTTTCGGT | 11252 |
| rs560667900 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882516 | AGCTTTAAATCAAAC[C/T]AGCCAAGCAGGTGGC | 11252 |
| rs560699118 | in-del | -/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870454 | GACGAGTGCTTTAGA[-/T]TCTCTGAATATCAAA | 11252 |
| rs560704876 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906677 | CATTCCTGAAAAAGG[C/T]AGGTATACAGTGCTC | 11252 |
| rs560720709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971984 | AGGAGCCCCTCTGCC[C/T]GGCCGCCACCCCGTC | 11252 |
| rs560742536 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974784 | AAGAAAAGAGAAGAA[G/T]GAGGAGGAGGAGGAG | 11252 |
| rs560754511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968795 | TCCTGCCTTGGGCCA[C/T]GGAACCCCAAGCTTG | 11252 |
| rs560765364 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886167 | CCCTGCTAGCCCCAA[A/G]TCCTGCCCCCAGCAC | 11252 |
| rs560803904 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880476 | CTGATGGGAAGGGCC[A/G]GCTCTCAATACCCCT | 11252 |
| rs560814733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917098 | CCCATGCACTACACG[C/T]GTGCACTCCATTTAG | 11252 |
| rs560822945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882737 | AGCGTGAAGATGACC[C/T]GGTGCTGAACACACC | 11252 |
| rs560829817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937946 | TCTGGAATGACAGCG[A/G]TAGAAGTCTCACCTG | 11252 |
| rs560842206 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014283 | GCTTGGCCCCAGCCC[A/C/T]AGGACGTGCTGCGGT | 11252 |
| rs560861680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877597 | AAGAAGATTCCTTTG[A/G]TGCTCCAGAGGGAAA | 11252 |
| rs560879358 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012814 | TGAGCACCACCACAC[C/T]CAGCTAATTTTGTAT | 11252 |
| rs560887156 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901273 | AACCAGAGTCAAATG[G/T]TTTATCCAAAGCTGA | 11252 |
| rs560919683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895286 | GGCCTTACTGTCATT[C/T]TGAAATTTACAGCAG | 11252 |
| rs560927051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963551 | AGGCCTTTTGTTATA[C/T]GATTGTCGCATGGTA | 11252 |
| rs560955490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982644 | AAGGGCGGTGCAAGA[C/T]GTGCTTTGTTAAACA | 11252 |
| rs560958224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889684 | GGTGGCACATCTACC[A/G]TCTACTCCATTCCAG | 11252 |
| rs561024653 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963965 | CCCATTTAAAGGGCA[C/T]AATTCAATGTTATTT | 11252 |
| rs561025509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009603 | GGAGTTCTGTGCTGA[C/T]TGTCCCAGACCTCAG | 11252 |
| rs561080829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990490 | CCATACATGAGGAGT[A/G]TGGGGACGGGGGTGG | 11252 |
| rs561093337 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888491 | GTGCTAGGGCACTCA[C/T]CTGTGGCCTTCTTGA | 11252 |
| rs561098387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991012 | CTCAACGGGTTCTAT[A/G]CACAAAGTGCTTACA | 11252 |
| rs561126106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959643 | TGAACTAATTGAACA[C/T]TGCCGTCACGGAGCT | 11252 |
| rs561126852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902144 | CCCTCATGGAACTTA[C/T]GGCCAGAAAAATAAT | 11252 |
| rs561130184 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015122 | GGCAGCACTGCCCAG[C/T]CCTGCCCAGACCCCT | 11252 |
| rs561142066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975348 | AGGGGGCTGGGCATG[A/G]TGGCTCATGCCTATA | 11252 |
| rs561150566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926200 | AACATGGTGTAGTAC[A/C]TTTGATTCAACAACG | 11252 |
| rs561167218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957186 | ACTAGAACACCAGGA[A/G]GGAAGACAGTTCTGA | 11252 |
| rs561178505 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913467 | CTGGGCAACAAGAGC[A/G]AAACTCCGTCTCCAA | 11252 |
| rs561199315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008744 | GCGGCTCTGGGCCCA[A/G]GGAGGGGCCTCCTAG | 11252 |
| rs561203025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963080 | AGAGCCTAAGCTGGA[A/T]TTCCAGTTCTGATCT | 11252 |
| rs561205270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890158 | AGGTGCCCGCCACCA[C/T]GCCCTGCTAATTTTT | 11252 |
| rs561210531 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872198 | GGAACTGATGGATCC[G/T]GGTCTCAAGGAGGCA | 11252 |
| rs561211687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919920 | CCACCCTGGGCAACA[C/T]AGTGAGACCACCATC | 11252 |
| rs561211990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926670 | CCCTCTTCTTCCCAC[A/G]GGAAAAAAAAAAAAA | 11252 |
| rs561215767 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934346 | AAGACCTTCAAGGCA[C/T]TGTGTGTGTGCAGAT | 11252 |
| rs561269272 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957266 | CATAAATTAAAATAG[C/T]TGTAAAGTTATTAAA | 11252 |
| rs561269362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907739 | TGCTCTCCATACAAC[A/G]CTGGCTCTAGGAGGC | 11252 |
| rs561285038 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015879 | AGAGGATGGTGAGAG[A/G]AACCCCAGGTGAGGG | 11252 |
| rs561334195 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004897 | CTTTAGCTCTGACTC[C/T]CTTTCTCCTCTAAAC | 11252 |
| rs561339340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984852 | AACAATGAGACCCCA[A/C]AAGAGGCAACTACTT | 11252 |
| rs561351873 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884911 | CTCAAGCCTCAGATC[G/T]GGCCCACAGCAAAGG | 11252 |
| rs561371609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907606 | GTCCGTTGGGGTCGG[C/T]GTGCGTGGAGGCGGC | 11252 |
| rs561388993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945007 | GGAGGCTGAGGCAGG[A/G]GAATCACTTGAACCT | 11252 |
| rs561409867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003444 | CCGTCTCTACTAAAA[A/G]TACAAAAAATTAGCT | 11252 |
| rs561424696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999061 | TCTTCCTGGACGCCA[C/G]ATAATTCGGGATGCT | 11252 |
| rs561451898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976358 | CCACTGGCAAGCGCA[A/G]GCCTTAATGCACACT | 11252 |
| rs561456896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951614 | CAGGACAAATGCCCC[A/G]GTGTCATCCCTGACT | 11252 |
| rs561462960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914333 | TGCTTCCCAGGTTCA[A/G]GCAACTCTAGTGCCT | 11252 |
| rs561484149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993106 | TTCAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGT | 11252 |
| rs561486089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999470 | AGGTTGGGAATTCAA[A/G]ACCAGCCTGACCAAG | 11252 |
| rs561501505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945508 | ACAGTCCTTGCAAAC[C/T]ATCCCCTTCCCTATG | 11252 |
| rs561512422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952550 | TATTTTTAGTAGAGA[C/T]GGGTTTTCACATTGG | 11252 |
| rs561525744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908058 | CCCAGAATATTTGAC[A/G]CAAGATACTTATGTT | 11252 |
| rs561525875 | in-del | -/GGGAGCT | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993058 | TAGTCCCAGCTACTC[-/GGGAGCT]GGGAGCTGGGAGCTG | 11252 |
| rs561528777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904509 | GTCCCTAAGCTCGCT[A/G]AAGACCTGAGGCTTT | 11252 |
| rs561550334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930280 | TGACATGCAGCCTAA[C/T]TCACACACTTTCCTG | 11252 |
| rs561566939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939066 | AGCAAAGGTAGGACA[A/G]GCCCCAAGGTCACCC | 11252 |
| rs561581050 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939815 | AACGAAAGGTCATTA[C/T]CACTGCATCCTCTAG | 11252 |
| rs561607409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899810 | GGATGTGCGCGACTA[C/T]GCCGACACACTGACC | 11252 |
| rs561616821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980431 | CACTCCAGCCTGGGC[A/G]ACAGAGAGAGACCCT | 11252 |
| rs561651064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875577 | GTCTTGCTCTGTCAC[C/T]CAGCCTGGGGTACAG | 11252 |
| rs561652047 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006763 | GAGGGTGCAGTGAGC[C/T]GAAATCGCACCATTG | 11252 |
| rs561658532 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917626 | TCTCAAAAAAACCAA[A/C]CAAACAAAAAAAAAA | 11252 |
| rs561688558 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946243 | TACCTAATATAATCC[A/T]GGGTAGGGTCTCCAG | 11252 |
| rs561688843 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870009 | GCACTGCTGAGTCAC[A/G]TGAAACACAGGTTCC | 11252 |
| rs561689675 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005904 | TAGGAAGTAGGGCCT[C/T]TGGAAGCTAATTAGG | 11252 |
| rs561723989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910998 | CAAGCTCCGCCTCCC[A/G]GGTTCATGCCATTCT | 11252 |
| rs561745263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900364 | CGACGGCGTCATAAT[A/G]GAGCATCCCATACTT | 11252 |
| rs561761340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960229 | AAGAGAAAAAAGACA[A/G]CATGCTCTCTCTGCA | 11252 |
| rs561782546 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882953 | CATGATCCCCTCCAT[C/T]AAGGGTTGAATTGTG | 11252 |
| rs561785560 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882563 | TCTGTGTCACATATG[C/T]AAAAGGCACCAGCAG | 11252 |
| rs561790789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947671 | TTCACAAGACCCCTG[A/G]GGGTGGGGGGGGGGA | 11252 |
| rs561806192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875040 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACACTCT | 11252 |
| rs561836432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942570 | TCTCTGATCCATCTG[A/G]AGTTAAGTTTTATAT | 11252 |
| rs561840760 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869304 | GGCTGGCTGAGACTC[C/T]TCAAGAAACCCTGGC | 11252 |
| rs561850916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910470 | GGGGGGCCAGCCAGC[A/G]GGACCTGATTACTGT | 11252 |
| rs561860194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987773 | TCTCCTGACCTCATC[A/G]TCTACCCACCTCCGC | 11252 |
| rs561870937 | in-del | -/TTC | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975620 | AGTATTCTTTTTTTT[-/TTC]CCTTTTTCTAACCAG | 11252 |
| rs561876629 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988000 | ACAAAAATTAGCCAG[A/G]TGTGATGGCACATCC | 11252 |
| rs561892584 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972179 | AAGATTCTTCTGCCT[C/T]GGGACGCTGTTGATC | 11252 |
| rs561899700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925248 | ACTTTGGGCGGCCGA[A/G]GCTGGCGGATCACTT | 11252 |
| rs561900191 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947986 | CCTCCTCCAACACAG[A/C]GGCCAAGAGCTAGGA | 11252 |
| rs561931573 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987148 | ACAAAACACCAAGAC[G/T]GACCTGGGTTCAAAC | 11252 |
| rs561948058 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918292 | ATGACTGAATTATAT[A/C]CCCCAAAGACAGCTA | 11252 |
| rs562046710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979159 | CAAAAACAATTCAAA[A/T]GTCCATACCACTGCC | 11252 |
| rs562056797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972376 | AACATTGCGGAAGGC[C/T]GCAGGGTCCTCTGCC | 11252 |
| rs562059538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875116 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 11252 |
| rs562066413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949500 | TTGTGATGCTAGCTG[C/T]CTAATAAACATTTCC | 11252 |
| rs562128680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007975 | AGCAGGTACTTCCAC[A/G]GGCAGCTTAATGGAG | 11252 |
| rs562145237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887119 | CCTCCCACTCAGTAG[C/T]TGGTTCCAGGCTCCT | 11252 |
| rs562161526 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919073 | AAGCTGCTCTTTAAT[A/G]CCAAACAGTGCTGGA | 11252 |
| rs562174030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012901 | TCTGGTGATCCGCCC[A/G]CCTCTGCCTCCCAAA | 11252 |
| rs562183579 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923837 | AAGCCAGGAATTCAA[A/G]ACCAGCCTAGGCAAG | 11252 |
| rs562212709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007431 | ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGGC | 11252 |
| rs562219749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933834 | AATAAGATATTCTGA[C/T]TGTAAGGAATTGTAA | 11252 |
| rs562228027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000786 | CAAAGGATAAAACTG[A/G]AATTGATTATATCCT | 11252 |
| rs562260863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925892 | GGGCCCTCTATGTCA[C/G]CAGCCTTGGCTCAGC | 11252 |
| rs562264838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918395 | TTTCTAGAAGTGGGA[A/T]AAACCACCATCCAAG | 11252 |
| rs562265931 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870889 | GCCATAATTTAAGTA[C/G]AAATGAACAGGTGTA | 11252 |
| rs562285698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927463 | CATGTTGGCCAGGCT[A/G]GTCTCAAACTTCTGG | 11252 |
| rs562286785 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961515 | GGTGGCTCACACTTG[C/T]AGTCCCAGCACTTTG | 11252 |
| rs562299828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931527 | GAGGAACACAGTCAG[C/T]GTCAATGGAACCAGC | 11252 |
| rs562314079 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898595 | CTTTCTAGGGTCCTC[C/T]GGAGGCCGCTCTCCT | 11252 |
| rs562345619 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001183 | GCTGAGCAGGGATTT[A/C]TCAGGGAAATAAAAT | 11252 |
| rs562354406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955225 | TGGATCCCTAGAGTC[C/T]AGCACAGTGCCTGAT | 11252 |
| rs562389360 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870482 | AAATAATATATACAG[A/G]TAGACACTGAGACAT | 11252 |
| rs562404695 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015703 | TGGATGGCAAGGCAC[C/T]AGGCAATGCACACGC | 11252 |
| rs562406544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994616 | TGGGGGTTACTGGGG[C/T]AGGGAATTCCAGGGT | 11252 |
| rs562457750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975541 | TTGCAGATTACTTAT[A/G]AGTCTCTTTTTATAA | 11252 |
| rs562460890 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957336 | AGTTTTCCTGAAGTG[C/T]TTTTGTTTCAGAAAT | 11252 |
| rs562462367 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933328 | GAATAATCCTGCATG[C/T]CTGGAGGGCGGGCAA | 11252 |
| rs562464083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907309 | AGGGAGCCATCCAAT[C/T]TGCTTTTCTAGATGG | 11252 |
| rs562497266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984751 | TTTGACACTTACAAG[A/T]TTATCTTAACACAAG | 11252 |
| rs562520407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964249 | ATAGTGAAACCCTGT[A/C]TCCACTAAAAGTACA | 11252 |
| rs562539803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896760 | TTCCCTGTCCTGCAT[A/G]CTCCCAGCACTTAGT | 11252 |
| rs562559135 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914793 | AGCCACTTGGGCAGA[A/C/G]GAATTCAGATTCTGT | 11252 |
| rs562568450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952732 | CAGTGGAGCGATCTC[A/G]GCTCACTACAATCTC | 11252 |
| rs562568655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946311 | GAAGTAAGGACAAAG[C/T]TAATAAAGCCAAAGG | 11252 |
| rs562576070 | snp | A/G | 0.00026898 | 0.0115939 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890913 | GTGCCAGGCAGAGCA[A/G]GGCCGGGCAGGGAAG | 11252 |
| rs562579352 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883955 | GAGGTTGCAGTGAAC[A/T]GAGATCACGCCACTG | 11252 |
| rs562623582 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872880 | CAGGGCAGCAGCCAC[A/G]ATGAACCACCATCTC | 11252 |
| rs562694837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991756 | ATTAGAAATTTTCCC[C/T]CAAAATTTTGGGGAC | 11252 |
| rs562720799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921885 | CTGGGATTACAGGCG[C/T]TCACCACCATGCCAG | 11252 |
| rs562743723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971549 | GCCTGGCAGCCCATC[A/G]TCTGGGATGTGAGGA | 11252 |
| rs562754732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879250 | TCAGTTCCTGCCCAG[C/T]GAGCCTGCAGTTGGC | 11252 |
| rs562805993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988301 | CAGTTACAAAGCCCA[C/T]GAGGACACAGACAGC | 11252 |
| rs562825602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998088 | CTTTAAGTCTGAGGT[C/T]TGGATTTGAGAATTA | 11252 |
| rs562828271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915544 | TGGCCACAGCTCAAT[C/T]TGTAATAACATCAGC | 11252 |
| rs562830870 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940074 | GCAGCCTGCTGCAGG[A/G]AAGCTCCTCCGAAGG | 11252 |
| rs562843520 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004056 | ATGTTTCTCAGAGGT[G/T]GGGGAGAAAGATTAA | 11252 |
| rs562861688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909215 | CCTGGCATGATGACC[C/T]GCCTAGTGTCTACCT | 11252 |
| rs562873869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909755 | ATATACACTGGCAAC[A/G]TTCACCTGAATGTTT | 11252 |
| rs562876408 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891321 | TATTTTTCTCTCAGG[C/G]ACTCTGTGCCTTTTT | 11252 |
| rs562876681 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003431 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 11252 |
| rs562930624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903845 | CAACTTGGGGTTTTC[A/C]GTTCTTGCTCCCAAC | 11252 |
| rs562935919 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877196 | GCTGTGAAACACGGT[C/G]CAGGAGCCTAGGAGA | 11252 |
| rs562972273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955534 | CATAGCCTCACATCA[G/T]GACTTTTCATCATCA | 11252 |
| rs562987320 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977170 | AGAAACAAACATTTT[C/T]ACAAAGAAATAGAAA | 11252 |
| rs563014858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892879 | TGTAATCAGTCAAGT[C/T]CCCCTTCCCTGCTGG | 11252 |
| rs563018034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935109 | TTTTTTTATTTTCAG[C/T]AGAGTCGGGGTTTCA | 11252 |
| rs563029848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986131 | ACACAGAAACAGTAA[A/G]CATTAGGCAAGGGAA | 11252 |
| rs563062405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934812 | CCCTAGTGCCTATCA[C/G]GGTACCCACAGCTCC | 11252 |
| rs563133673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982335 | CCTACTGGGAAGTGA[A/G]GAGCCCCTCTGCCCG | 11252 |
| rs563138297 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017436 | TCCTGGGCTCAAGCA[A/G]TCCTCCTGCCTCATC | 11252 |
| rs563153862 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994528 | TTTGGCTGGAGGCAC[A/G]TGCACACAGTGCACA | 11252 |
| rs563154804 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929009 | TTTAAGACAGCCTCC[C/T]ATAAGCAGGAGATTA | 11252 |
| rs563226388 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949461 | TCATACACACACGCG[C/T]GCGCACGCACACACA | 11252 |
| rs563231572 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001055 | CAAATAAAACTTAGG[C/G]CAAGGGCTGCTATGG | 11252 |
| rs563233703 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949334 | GCCTCTCTGGCAACT[C/T]CCACCCCACACAGGG | 11252 |
| rs563262361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911650 | CTCCTTGTTTCTACA[C/T]AAAACTCAACAGTAA | 11252 |
| rs563289719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008148 | CAGCTTTCAGAAATA[A/C]ATCAGAAGTATTCTT | 11252 |
| rs563310758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987976 | TGAAACCCCGTCTCT[A/G]CTAAAGATACAAAAA | 11252 |
| rs563316197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929563 | AGAATGAGTATCTCA[A/G]AACTCCAAAACGATC | 11252 |
| rs563317230 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946842 | TGACAGATGGCCACA[A/G]ATACAGGAGACATGT | 11252 |
| rs563322753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948787 | GCTAGAGCCAAAGCA[C/T]TCTACTGTAGAGAAG | 11252 |
| rs563332188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889591 | CAGAGAAAACCATCC[C/G]GAAGGACAGAGGCAT | 11252 |
| rs563335424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906268 | GGTTAAAACCCATCA[C/T]ATCATGAGAAAAACC | 11252 |
| rs563336767 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901208 | GCCAGCTATCCCAAG[C/G]TGACCTACAGAAGAG | 11252 |
| rs563357537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900501 | TATTATTTTATTTGC[A/G]AGAAGGGTCTCACTG | 11252 |
| rs563373324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894766 | CTGGCTTGAAAGGCT[A/G]CAGTCGCTGATAACT | 11252 |
| rs563383722 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921611 | GAGAAATTCTAATGA[A/T]ATCTGATGAGAATTC | 11252 |
| rs563392980 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926330 | CCAGAAGCACCCATC[C/G]GCCTGGGCAGGGTGG | 11252 |
| rs563432132 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011836 | GGCCAACATGGTAAA[A/C]CCCCATCTCTATTAA | 11252 |
| rs563436207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937054 | CCTGTGCAGCCACAC[A/G]GTGTTCTGAATGCTG | 11252 |
| rs563483109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002680 | ACCCTTTAATACAAG[A/C]TTTCTATTCTCGGGA | 11252 |
| rs563487161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926004 | TAAGCCAGTGGGCGC[A/T]CAGGAAGTAAGGCCC | 11252 |
| rs563491163 | snp | G/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896746 | GCAACGTATGAGACT[G/T]CCCTGTCCTGCATGC | 11252 |
| rs563499295 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941891 | AAGCGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 11252 |
| rs563510169 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994085 | AGCTCTCAAGAAGAC[C/T]ACGATGTAGACTGGA | 11252 |
| rs563517008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008583 | CATATATGAGCTCTT[A/T]ATATAGCTCAGAATG | 11252 |
| rs563518908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968761 | TCTATCAATGTCCTG[A/G]AGCTGGGATGCACTC | 11252 |
| rs563528618 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874773 | CCTGCAATTCACAGC[C/G]TTGGCCCAGCAAGGT | 11252 |
| rs563547625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919875 | AAATCTCAACACTTT[A/G]AAAGGCCAAAGCAGG | 11252 |
| rs563550458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931641 | CACAGAAATCCCCAT[A/G]TGGTTTAAACTTGAT | 11252 |
| rs563557328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013658 | CAGGAGGGTTAAAAC[A/C]GAACTTCAGCACACG | 11252 |
| rs563561410 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913937 | GCTTAATCTGGTGGA[C/T]TGCAGAGCTCCTAAA | 11252 |
| rs563564242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907713 | AGGGCACTGCTCTGC[C/T]GCCTCCTAACTGCTC | 11252 |
| rs563579890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937821 | CCCTAGGGGGTCACA[C/T]GATCTGAAGACCAGT | 11252 |
| rs563637305 | snp | A/G | 3.35087e-05 | 0.00409307 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871515 | AGAGGTATGACACCG[A/G]CGGTGGGCTACAGAG | 11252 |
| rs563694540 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923136 | GCTGCATGGTAACTC[-/A]AGAGTTTTGTACCCA | 11252 |
| rs563699362 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984330 | GAAAAGAAACAACTA[C/T]ATAATTTGTTTAAAG | 11252 |
| rs563720047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011405 | CAGGCCCGAGTCAGC[C/T]GGGAGGTTCACATGA | 11252 |
| rs563727884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892192 | GGGGTAGGGTGGGGT[A/G]GCGTGAGGCTGGAGG | 11252 |
| rs563734433 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894787 | GCTGATAACTTGAGC[A/C]CCCAGAGGAAATATG | 11252 |
| rs563764729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885260 | GTGGGGATGTGCCTC[A/G]AGGTCAATGACCTCA | 11252 |
| rs563773463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009437 | ATCACAGGTGAGAGG[A/G]AGCTTAGAGATGGAA | 11252 |
| rs563776281 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965374 | CCACTTGTCAAAGCT[C/T]CTAAAAGGATGCATT | 11252 |
| rs563808585 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878012 | TGGCAAGTGGTACTT[C/G]ACCTAGGCCTGCTGG | 11252 |
| rs563818577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944868 | TTTGGGAGGCCAAGA[C/T]GGGTGGATCACCTGA | 11252 |
| rs563833224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920516 | CTTTTTGGAAAGAAA[C/T]AAATTCAAGGGAGGC | 11252 |
| rs563846954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995509 | GTCCATTGGGCAGGA[A/C]CTTAAAAGTCACAGC | 11252 |
| rs563868872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878395 | TTCTTAGGAAGCCCC[C/T]GTATGAAATGACTAT | 11252 |
| rs563879127 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921905 | CACCATGCCAGGCTA[A/G]TTTTTGTATTTTTAG | 11252 |
| rs563915303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884827 | CCCAGAACTCAGTGT[C/G]TATGGTCTTGAGCGT | 11252 |
| rs563944439 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999069 | GACGCCAGATAATTC[A/G/T]GGATGCTGAACCCAA | 11252 |
| rs563956622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879362 | TGAACCCAAACGACC[G/T]GAGCCCCTCCTCACT | 11252 |
| rs563957772 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995338 | TAAAGAACAGGCTGC[-/T]TTTTGGTGCCAGGAG | 11252 |
| rs564063026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928953 | TGAAAAGAAGAGAGT[A/G]GGATTCAACAAGCTC | 11252 |
| rs564068892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998467 | CACAGAGCAAGAAAA[G/T]GGCAACAATAAACTT | 11252 |
| rs564095394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971511 | CCGGCCGCCACCCCA[C/T]CTGGGAAGTGAGGAG | 11252 |
| rs564106875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935267 | AGAGTCCAGCAGTGT[C/G]TGCGCCATATTCCTG | 11252 |
| rs564126652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904014 | AGACACACTGAGTTA[C/T]GAATCTTTAACTGAA | 11252 |
| rs564165264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874975 | CCTGCGTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 11252 |
| rs564176573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879968 | CGAGTTCTCGGGTGG[C/T]GAACTGGCTTCACCA | 11252 |
| rs564213428 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874571 | GCCCAGGGGCATGCC[A/G]AGTGCTACTCTGGGG | 11252 |
| rs564221491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935681 | AGGAAAAAGTGTTTC[C/T]ACAGAGACAAGGGCA | 11252 |
| rs564226857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947908 | CCAGCTCCTGAGCCC[A/G]TAAGCCAGGTGCCCC | 11252 |
| rs564264932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998960 | TCCCACTCCATCCCA[A/T]CTCCAGCTCCCCATC | 11252 |
| rs564293099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931061 | ATTCACTCATTCATT[C/T]GCTCAGTGTTCACTG | 11252 |
| rs564333023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972041 | AGAACGGGCCATGAT[G/T]ACAATGGCGGTTTTG | 11252 |
| rs564400377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961416 | ACCCTGCCAAATCCC[C/T]CTCTGTGAGAAACAC | 11252 |
| rs564442582 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904493 | CGAGATCACCTGCCC[A/G]GTCCCTAAGCTCGCT | 11252 |
| rs564454261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955045 | ACAAACCACTCCCTC[C/T]AAAACTCATCATCAA | 11252 |
| rs564464326 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923669 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 11252 |
| rs564464431 | snp | A/C | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897143 | GGTTTTGCCGTGTTG[A/C]CTAGGCTGGTCTTGA | 11252 |
| rs564468949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986975 | TGTAAATCACACATA[C/G]CTACACGCACACATA | 11252 |
| rs564470465 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978435 | AGTCTTCGTTTACAC[A/G]CAACACAAGAAGAGC | 11252 |
| rs564486991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893049 | AACTCAGAAAGACTG[C/T]CAGGTGTTGCCAGCT | 11252 |
| rs564504784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012881 | CTGGTCTCGAACTCC[C/T]GACCTCTGGTGATCC | 11252 |
| rs564510570 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944317 | GTTACTGCAATGTAA[C/T]CTAGCTAAATATAAT | 11252 |
| rs564525051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893318 | TAAAAATCACACCCC[A/G]CTCTGGAACTGGGAA | 11252 |
| rs564533748 | in-del | -/A | 0.39979 | 0.200158 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975656 | TTGTCAATATTCTTT[-/A]AAAAAAAAAAAAAAG | 11252 |
| rs564571276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967599 | GGTGTTTAGAAACCC[C/T]GCAAATGGGCCGGGC | 11252 |
| rs564576806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972366 | CAGGGACATAAACAT[G/T]GCGGAAGGCCGCAGG | 11252 |
| rs564591970 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008141 | TTCAAAACAGCTTTC[A/G]GAAATACATCAGAAG | 11252 |
| rs564592051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881387 | GTTTGCTCAGCTTCC[A/C]ACAGGTGGTCAGAGG | 11252 |
| rs564613760 | snp | G/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876461 | TTCCGAAGGAGCACA[G/T]GTGGAGCCAGTGCTA | 11252 |
| rs564631278 | snp | C/T | 4.96973e-05 | 0.00498459 | missense | PACSIN2 | GRCh38.p7 | 22:42876224 | CCGAGGTGGCGTCGT[C/T]GTCGAATGGATTCGA | 11252 |
| rs564638435 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006893 | AAATGCAGGTTAAGA[G/T]AATGAGTCAAGGCTG | 11252 |
| rs564647705 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933162 | AGGAAAACCTTGTTA[A/C/T]CCCTGAAAAGTTGAG | 11252 |
| rs564649225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012392 | AGAGATGTGGATGGG[C/T]ATCCAGGATTAGGGA | 11252 |
| rs564663202 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945723 | CTGTCCCCATGATGA[C/T]AGCTACCTTCGCTAA | 11252 |
| rs564690132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967179 | AGATGTGAGAAGATG[A/C]CCAGGAAGGCTGGAC | 11252 |
| rs564695371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887606 | AGGGCAGGCCCTCGG[C/G]AATCACACCCCCCAG | 11252 |
| rs564703912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901662 | GCCAGCTGTGCTCTC[C/T]GCCTGCCACGGCGAT | 11252 |
| rs564731265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880752 | CACAGAGAGAAGGAC[C/T]CCCTAGGCTCTGGCT | 11252 |
| rs564750530 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999691 | AAAATGCTGTCTACA[C/G]ACTATGCCTGGTGGG | 11252 |
| rs564797235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975397 | GCTGAGGCAGGAGAA[C/T]TGCTCGAGCTCAGGA | 11252 |
| rs564813162 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967639 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 11252 |
| rs564813906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000623 | CGTACACCCAAAAAA[C/G]TTTAAGGAAGGTGAC | 11252 |
| rs564838024 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872255 | ACTAGGGTAGGGCCC[C/G]AGGTCTGGCATTTGC | 11252 |
| rs564856015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958215 | AGACTCACTCGGCTA[C/T]CAACGAGACGAGTGA | 11252 |
| rs564862525 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927744 | AAGCATGCACCACCA[C/T]GTCTGGCTAATTTTG | 11252 |
| rs564867237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983331 | CAAAAAAAAAAAAAA[A/G]AAAAAGAAACTGGCT | 11252 |
| rs564923912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889714 | GCTAGGAATGGGGGG[C/T]GAGGCTGCAGGCAGG | 11252 |
| rs564929662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895965 | CCTTTCCACTTCCCT[A/G]GGCAAAGCACTGCAG | 11252 |
| rs564971286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932410 | ACCTCAGTTTTTACC[C/T]GTGTACAGTCTGCTT | 11252 |
| rs564978797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872826 | ACCAGTGCGCCTGCA[C/G]ATCTAACCCAGAGGC | 11252 |
| rs565070261 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893824 | ACACATCAGTGAACG[A/G]GGGCTTCTCAATGTT | 11252 |
| rs565109605 | in-del | -/CT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918619 | ACCCAGACCATCAGA[-/CT]CCACGCTGCCCAACT | 11252 |
| rs565111279 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891787 | TAATTTACTTAAAGG[A/T]GGCCAGAGAAGGGGG | 11252 |
| rs565115767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896998 | CTAGAGTGCAGTGCC[A/C]CAATCATGGCTCACT | 11252 |
| rs565116714 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967026 | ATAATTAACTTAAAC[A/G]AACTTGTCCGTAAGC | 11252 |
| rs565131660 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970246 | ACATCACGGTGGTGA[A/G]TCATGGCAGTATCAG | 11252 |
| rs565132220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985410 | CCTGATGGGCTCCAC[A/G]TTCTGCCCACAAGGG | 11252 |
| rs565150355 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883884 | TGGCGCATGCCTGTA[A/G]TCCCAGCTACTCGGG | 11252 |
| rs565159661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002964 | GAAACAGCGAGGTCA[A/G]TTCAAGCTCCAGATC | 11252 |
| rs565164011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920646 | GTGCTGGAAGAGAGC[A/G]GCCAGGTGTGCACCA | 11252 |
| rs565171993 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927439 | TTTTTAGTAGAGACA[C/G]GGTTTCGCCATGTTG | 11252 |
| rs565178294 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963347 | CAGAGAGTCCACCAA[A/G]TTAACTAAAGACCAG | 11252 |
| rs565185880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878868 | ATGCCCCTGGGCCAC[A/G]GCCCACAGAGCTCAG | 11252 |
| rs565211673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977487 | ATAGAAACAGAATGG[G/T]GAAAAACAGTTTTTA | 11252 |
| rs565223331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003632 | CAAAACAAATATCTG[C/T]TCTAATATACCTGAG | 11252 |
| rs565226246 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985205 | TGGCGGCACATGCCT[A/G]TAATCCCAGCTACTT | 11252 |
| rs565230467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921178 | TCTTGGCTAACACGG[A/T]GAAACCCTGTCTCTA | 11252 |
| rs565241962 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913625 | ACTGTTATACACCCT[G/T]AGTAAGTGCTACGAA | 11252 |
| rs565242014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914530 | GTGAGCCTTTTTTCT[A/G]TGGAATCCTATGCTG | 11252 |
| rs565273901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902793 | TAATTTTTGTATTTT[C/T]AGTAGAGACAGGGCT | 11252 |
| rs565294667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993186 | TCAAAAAAAAAAAAG[A/G]AAGAAGAAGAATACA | 11252 |
| rs565303185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997782 | CTCGGGAGGCAGAGT[A/G]AGGCAGGAGAATCAT | 11252 |
| rs565339556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898775 | GCCAGGCTTCTAATC[A/G]TTCCTCTGAGAACCC | 11252 |
| rs565347188 | in-del | -/CTCCCC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980482 | CCTCTCCCTCTCCCT[-/CTCCCC]CTCCCCCTCCCCCTC | 11252 |
| rs565374654 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869349 | TCTGTTTCCTCCTCG[G/T]TAGAATGGAAATGGG | 11252 |
| rs565390444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898460 | ATTTTTAGTAGAGAC[A/G]GGTTTTCTGCATGTT | 11252 |
| rs565402023 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916847 | CTGACACCCTAAAAG[C/T]GATAGCCATTGTTCT | 11252 |
| rs565414182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909135 | ATCCAAGTGCAGCAA[C/T]GTCCACTACCCCATG | 11252 |
| rs565414670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971141 | CTGATGCCGAGCCAA[A/C]GCTGGACTGTACTGC | 11252 |
| rs565445331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939962 | CGGCGTCTACCCGGC[C/T]TTCAATAAACTACTG | 11252 |
| rs565454006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903263 | TTCCCTGGGGAGGGT[A/G]TGCGTGTGCCTGGCA | 11252 |
| rs565517807 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957640 | TTTATTTATATTATG[C/T]TGTATTATTTTAAAG | 11252 |
| rs565544763 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942437 | GAAAACACTGCCTAA[C/T]CCAAGGTGACAAAGA | 11252 |
| rs565555946 | snp | C/T | 1.67293e-05 | 0.00289212 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42893503 | CCACTCAGTGAGCTG[C/T]TGCGCATACGCCTTC | 11252 |
| rs565557697 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012144 | GCGAGACTCTGTCTC[A/T]AAATAAATAAATACA | 11252 |
| rs565558149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934362 | TGTGTGTGTGCAGAT[C/T]GCCTTTTCCCTTCTT | 11252 |
| rs565569364 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947682 | CCTGGGGGTGGGGGG[C/G]GGGACCTCTTAATGA | 11252 |
| rs565616716 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016972 | GGCTAACATGGTGAA[A/C]CCCTGTCTCTACTAA | 11252 |
| rs565697263 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011963 | CATACTGGCCAACAC[A/G]GTGAAATCCCGTCTC | 11252 |
| rs565699077 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964364 | TGGAGGTTGCAGTGA[G/T]CCAAGATCGTGCCAT | 11252 |
| rs565707190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007530 | CACTCCTTGTTCTTC[A/G]GAGCTCTGTAGCTCT | 11252 |
| rs565737941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941623 | TTGTGATTTTGATTC[A/G]TGTTTCCCTAATGAC | 11252 |
| rs565744751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972478 | CCAAATCCCCCTCTC[C/T]GAGAAACACCCAAGA | 11252 |
| rs565782704 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996696 | GGCCCTGTCTCAATC[-/AG]GGGGAAAAAAAGCAG | 11252 |
| rs565783638 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909560 | GCACTGCGGAGTTGA[G/T]ACCAGCTGGAGAGTA | 11252 |
| rs565801849 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936477 | ATCTTTAAGTCCTAT[A/G]AAGACTCAAACATTC | 11252 |
| rs565821664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911343 | TGAGCCCAGGAGATC[A/G]AGGCTTCAGTGAGCC | 11252 |
| rs565823500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918598 | TAAGTGCTAGGCTGA[C/G]ACTCAACCCAGACCA | 11252 |
| rs565829462 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955476 | GATAGCATCAGGGGG[-/A]AAAAAAAAAAAGGCT | 11252 |
| rs565842346 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939090 | GTCACCCGTCCCAGC[A/G]CAGCCCATCAGCTCT | 11252 |
| rs565846366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923986 | ATTTGAGGCAGCAGT[A/G]AGTTACGATTGTGCC | 11252 |
| rs565861599 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972069 | TTGTCCAATGGGGGG[A/G/T]GGAAATGTGGGGAAA | 11252 |
| rs565885910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886566 | GAACTCCTGGGCTCA[A/G]GCAATCCTCCCGCCT | 11252 |
| rs565889580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966573 | TGTCCAAAGATTTTT[G/T]TAACAGTGAAGTGAG | 11252 |
| rs565901832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930071 | AGCACAAAGTTCGCC[A/G]TGTTAAATATGAATG | 11252 |
| rs565916554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935896 | CCCAGGTACATTCTA[A/T]CACTTCATTCTTCCT | 11252 |
| rs565925052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880938 | CTGTGCACAAAACAC[A/G]TCAGCCAAGACTTCC | 11252 |
| rs565938795 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960668 | GCACAAGAAAAGGCG[C/T]AACTAATCTACACCC | 11252 |
| rs565951821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967221 | TCACGTAAACAAGGG[C/T]CGTGTCCTGCTGCAC | 11252 |
| rs565955614 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940401 | GTGTTTGCTGAATGA[C/G]TAACACTGTTCCTGT | 11252 |
| rs566006625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964311 | TAATCTCAGCTACTC[C/G]AGAGGCTGAGGCAGG | 11252 |
| rs566024829 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936628 | ATAAAGATGGGGTTA[C/T]GGCTGGGCATGGTGG | 11252 |
| rs566032087 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892033 | AGAATGGAAGCCCAT[A/C]CTGCAGGAGGAAGGA | 11252 |
| rs566062756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961046 | ATCTAAGTGGTAATG[C/G]CCAGGGCAGGGCCAG | 11252 |
| rs566085584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994277 | AACCCCACCTCCCCA[A/T]GCAACTGGGGCTCCA | 11252 |
| rs566104783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920760 | AAAGTTGTGAGTGGC[A/G]GGGGTGAGGGTCAAT | 11252 |
| rs566108820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010327 | GAGGATCACTTGAGG[A/C]CAGGGGTTTGAGACC | 11252 |
| rs566113466 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900627 | ACAGGTATGTACCAC[C/T]ACACCTGGCTAATTT | 11252 |
| rs566119241 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948388 | GCATGGACAAGAAGA[C/G]GTCACACCCATCAGA | 11252 |
| rs566125885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961681 | AGGAGGCTGAGGCAC[A/G]AGAATCGCTTGACCC | 11252 |
| rs566142323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876411 | CCCCGCAAGGGGAGG[A/G]CACTGGAGCCTTGGG | 11252 |
| rs566144801 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978995 | GCTGGTGACCTCAGA[A/G]CTCTGACCAGTATAA | 11252 |
| rs566145359 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900778 | CGCACCCGACCTAGT[A/G]TCCCTATTTTAGAGA | 11252 |
| rs566179142 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870569 | TTTTAACTCTGAATC[A/G]GTGATAAAATTGTTA | 11252 |
| rs566231937 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911251 | GCTCCAGGGGTTTTG[C/T]CACAGGGACAAAATT | 11252 |
| rs566234598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988245 | CAAGGAGAAGATAGT[C/T]TCTGAACACTTTTCA | 11252 |
| rs566295363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989259 | ACCCAGCACTTTGGG[A/G]GGCGAGGTGGGTGGA | 11252 |
| rs566301223 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980292 | GCCAAGGCATGAGGA[A/C]TGCTTGAGCCCAAGA | 11252 |
| rs566350173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957795 | CAAAGAAGAATTGAG[C/T]GCTTGTCTGTTTCTT | 11252 |
| rs566365106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931412 | GGCTTCCAAGCCAGC[A/G]ACACCAAGGTGAACC | 11252 |
| rs566367699 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907685 | GACATTCGCTCGCTT[C/T]GTGCTTGCGCTCAGG | 11252 |
| rs566369640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880346 | ATTTTCTGACCAAAA[C/T]AGATTGACTGAGAAC | 11252 |
| rs566388376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939441 | AAGAAGATGTACAAG[A/C]GTCTAAAGATTTGAA | 11252 |
| rs566400014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973740 | CCTGCTACACTCCAG[C/T]CTTAGGCCTGGGCCC | 11252 |
| rs566413807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894326 | GCTCACTGCAACCTC[C/T]GCATCCCAGGTTCAA | 11252 |
| rs566427869 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914199 | TTCACAGAGGCTGGA[C/G]AGGCCACCTGGCCTG | 11252 |
| rs566451524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940138 | GCTCCACAGATGTTA[C/T]CTAGTACTATTCCTA | 11252 |
| rs566453238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883771 | AGCACTTTGGAAGGC[C/T]GAGGTGGGCGGATCA | 11252 |
| rs566528982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958457 | ATTGGCATAAATCTC[A/C]TACCTGTAAAAATGC | 11252 |
| rs566536842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971277 | TTTTTGGTGGAGACG[A/G]GGTTTCGCCGTGTTG | 11252 |
| rs566546608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878967 | CCAGGTGTCCAGGCC[A/G]GGGCTGCCCTGGACC | 11252 |
| rs566558866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996455 | GAGAATCGCCTGAAC[C/G]CAGGCAGCAAAGGTT | 11252 |
| rs566573871 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985140 | TCAAGACCAGCCTGG[A/C]CAACATGCGAAACCC | 11252 |
| rs566576992 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016405 | TGGAATCCCAGTACT[C/G]TGGGAGGCCGAGGCG | 11252 |
| rs566603997 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905629 | TTGATTTTTCCCAGT[A/G]TCGGGAATGGCTGAG | 11252 |
| rs566607486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914922 | GCTGGAGTGCAGTGG[C/T]ATGATCACACAGCTC | 11252 |
| rs566619453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908595 | GTGAAGCCTGTGGGC[A/G]GGCCAGACCAGGCTC | 11252 |
| rs566631199 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991332 | CTGGGTCTCAGCTGG[C/G]TGCAGGTCTCAAGGC | 11252 |
| rs566641475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951998 | TGCCTCCCAGCATCA[A/G]ATATTTGCTCAAACA | 11252 |
| rs566675214 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934198 | TATGGAAACGTGCAG[A/C]GAGCACTGAGGCTTT | 11252 |
| rs566685692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976585 | TATGTAGATTCTATG[A/G]CTGTTTTAGATTTTC | 11252 |
| rs566696958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991884 | AAATGGATCACAGGC[C/T]TAAATGTAAAACATA | 11252 |
| rs566712866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879544 | TCTCAGTCCCAGCCC[A/C]CTCAGGCCAGCATGG | 11252 |
| rs566734537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891276 | ATGTGGCCATTTAGA[C/T]CACAGAGGGTTTCCT | 11252 |
| rs566749706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880062 | AGTCTGTGCATGCCC[A/G]CAGGTGTTTAATGAG | 11252 |
| rs566751546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874196 | GCACACATCTGTGGT[C/T]CCAGCTACGTAGGAG | 11252 |
| rs566793040 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973941 | TACCAAGAACAGAAG[C/T]GTAGCCTTAACTTGT | 11252 |
| rs566813920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897157 | GCCTAGGCTGGTCTT[A/G]AATTCCTGGGCTCAA | 11252 |
| rs566813956 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903454 | CAAAGAGTAACAGGG[G/T]TCCTTGAAAAACCAT | 11252 |
| rs566823319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971657 | GCGTCTCTGCCCGGC[C/T]GCCCATCGTCTGAGA | 11252 |
| rs566831678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944740 | GAGCTATTTTCCATC[C/T]GAAATTGGGTATAAG | 11252 |
| rs566846174 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947455 | TCCACAAAAGAGGAG[C/T]GGCCTCTTCCCATGC | 11252 |
| rs566850539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898124 | GGAACCCAGGGCATG[C/T]GAGCCAAAAAAGGGA | 11252 |
| rs566855276 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017613 | AATCCCCCTGCACTC[C/T]AAGCACTGCTGAGTC | 11252 |
| rs566887675 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016576 | TCACTTGAACCTGGG[A/G]GGCGGAGGTTGCAGT | 11252 |
| rs566912398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884919 | TCAGATCTGGCCCAC[A/C]GCAAAGGTGGGGCTG | 11252 |
| rs566925612 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017105 | AGTGAGCTGATATCG[C/T]GCCACTGCACTCCAG | 11252 |
| rs566925793 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010974 | GGAACTGCAGAGATA[A/C]CAAAAAATGATGTAT | 11252 |
| rs566943347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885481 | GGTCTAAGCTTTGCT[G/T]TCCCTAACAACATGT | 11252 |
| rs566983131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922136 | GACTTCTGCCAGCAA[C/T]GTATGTAAGTACAGT | 11252 |
| rs567038971 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912470 | ACCCGGGATAAAACG[-/T]TGAGTGGAGGTAATC | 11252 |
| rs567044149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916101 | ATGTAATTTCTCTGA[A/G]CCCCAGTTCCTGAGC | 11252 |
| rs567044596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922749 | CATGTGCCAGGCACT[C/T]TTCTAAGCTGGGGGA | 11252 |
| rs567051455 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974175 | TCCGTATCCCTATGT[C/G]GACTCTGCTTCCGGT | 11252 |
| rs567053417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967788 | AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAATGG | 11252 |
| rs567109025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953094 | ATTAGCTGTATAAAA[C/G]ACAATGGCAAATTTG | 11252 |
| rs567120755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881644 | CTTGCATTTCGAATG[G/T]AAAGATAATGAAAGC | 11252 |
| rs567137299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998678 | AAACACGAGGCAGAA[A/G]GGCAGGGTCCCTGGT | 11252 |
| rs567155477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916659 | CTTGCAGTCCGCTCT[A/G]TGGCTCCTCCCATCC | 11252 |
| rs567170864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894301 | GCTGGAGTGCAGTGG[C/T]ACGATCTCGGCTCAC | 11252 |
| rs567187205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936450 | TCAGTTCCCTTGTTC[A/T]TGGAGCAGATGATCT | 11252 |
| rs567188230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947277 | CCACCTTCGAGGTCT[A/G]CTGTGCCAGGTTCCC | 11252 |
| rs567195732 | snp | A/G | 0.000264896 | 0.0115056 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876935 | GGTGCTGCCCGTGTC[A/G]TCCTCATCCTCGAAG | 11252 |
| rs567200800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910102 | GCCATACACAGAAGT[A/G]AGTGATCAGGTCAGC | 11252 |
| rs567202236 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002844 | ACAGGATAATATAAC[C/G]ATTAATAATCTTTTT | 11252 |
| rs567202319 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972470 | TGACCCTGCCAAATC[C/G]CCCTCTCCGAGAAAC | 11252 |
| rs567233333 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893706 | CAACCAGGCCCTGAT[G/T]CGCCCCTGGGGTCAT | 11252 |
| rs567244196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931275 | GGTAACCAGGGGCAC[A/G]TTACTTAACCTTCCT | 11252 |
| rs567253477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900607 | GCCTCCGAGTAGCTG[G/T]GACCACAGGTATGTA | 11252 |
| rs567269381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994990 | CCTTGCCCGTTTAGA[A/C]TGGAAATTCCATTTA | 11252 |
| rs567285376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995613 | TCCAATGTCATTCAC[A/G]CGGCAATTATTTGGA | 11252 |
| rs567322671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013147 | GAGATTAAAAGTGAT[A/G]AAGTTCCAAGTCCCA | 11252 |
| rs567364886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007664 | TGAGGACAGTCAGAC[C/T]CGCCCTCCTCTGTCG | 11252 |
| rs567380763 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964895 | AGTCAAGGACTAGCA[A/C]GACCCATGGCTTGGA | 11252 |
| rs567408423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013785 | TGATTTTCATCAAGA[C/T]AGCCAGGCAGTATTT | 11252 |
| rs567419290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955846 | ATCAGTCTACTACGC[C/T]CTGTGCTATTTTTTC | 11252 |
| rs567433831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001607 | GCTTGGGAAGCAAGA[C/T]ACTTGTATGCCTGTG | 11252 |
| rs567438667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925474 | GACAGAGCAAGACTC[C/T]GTCTTTAAAAAAAAA | 11252 |
| rs567445948 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010233 | TCAAGAAACACGCAA[A/G]TGATTTTTTTAGGAT | 11252 |
| rs567446683 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961807 | ATTCCTTAATGGAAA[A/G]ATACCAATAAAAGCA | 11252 |
| rs567450665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889017 | GGTTCGAGGCACCAG[A/G]AACACAGCAAGAAAC | 11252 |
| rs567500013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895701 | TTCAGGTTTCCAAAT[A/G]AGCTCCCAGTTGGTC | 11252 |
| rs567519693 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906747 | ACAGCCAAATACCAT[C/G]AGAAACACAACTCTC | 11252 |
| rs567536977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014786 | TCCCCGAGCCGACCC[C/T]ACTCGCCCTCGTCCT | 11252 |
| rs567551786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919460 | GGCACCCAGTGGTTG[A/G]CTGATTATTTCTTCC | 11252 |
| rs567586974 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007554 | AGCTCTGCCCAGAAT[-/G]GGTCCTTCACGTCAG | 11252 |
| rs567599421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002159 | ACAGAGCCAGGAACC[A/C]CCATGAGAGCAGCAT | 11252 |
| rs567607728 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907947 | GAGAGAAACCAGCCC[A/G]ACTCAGAGCAAGTTG | 11252 |
| rs567616637 | in-del | -/TTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983984 | TTTTTTTTTTTTTTT[-/TTTTT]GAGACAGGGTCTGGC | 11252 |
| rs567630570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956368 | AGGGCTGGAGGAGAC[A/G]TCAGGTAGACACAAC | 11252 |
| rs567647630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950083 | GAATCGAAAATATAC[A/G]GGGGAAAGAAGTGGG | 11252 |
| rs567647865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915106 | CTCCTGGGCTCAAGC[A/G]TTCCTCCTGCCTTGG | 11252 |
| rs567682455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998495 | CTTTTTCTGAACTTA[A/G]GCCTTTTAAAGATCA | 11252 |
| rs567689317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983540 | TAAATTATTGGTGTG[A/G]CATATGCAAAAAAAA | 11252 |
| rs567700337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871585 | CAGGCATTCTGTGGC[A/G]GGCAGGCCGAGGGCC | 11252 |
| rs567707951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943798 | TTTGAGAAAAGAAAT[C/T]TGTGATAATAAGGTA | 11252 |
| rs567718886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944403 | AACTTGTAAAATAAG[A/G]AAAATTAATATGACA | 11252 |
| rs567732563 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977637 | CTCACCCAAATCTCA[C/T]GGCAAATTGTAATCC | 11252 |
| rs567734167 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892212 | GAGGCTGGAGGGAGG[C/G]AGAGCCACAACGGAG | 11252 |
| rs567766933 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883905 | GCTACTCGGGAGGCT[A/G]AGGCAGGAGAACTGC | 11252 |
| rs567856896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975777 | TCTCCAGCTAGGAGG[C/T]TGGCTCCCAGGCATT | 11252 |
| rs567881324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938605 | GAATGCCTCTGCACA[A/G]GCCAACTGCATGTTC | 11252 |
| rs567906392 | in-del | -/AC | 0.00874735 | 0.0655527 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985654 | CAGCCCCTCCAACAG[-/AC]ACACACACAGACACA | 11252 |
| rs567919513 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950180 | ATAACTATTTACATT[G/T]TATTTATATTCTATT | 11252 |
| rs567921035 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974383 | AGGATGCCAGCTCCC[A/C]TTTGCCAATGATTTC | 11252 |
| rs567929428 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017301 | AGGCTCAAGCCATCC[C/T]CCTGCCTCAGCCTCC | 11252 |
| rs567944787 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955533 | ACATAGCCTCACATC[A/C]TGACTTTTCATCATC | 11252 |
| rs568008582 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874639 | GCAGTTGGGGACCCC[C/T]AGAGAAAGGCTTCTC | 11252 |
| rs568014216 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880049 | GATTTTCTAGAAGAG[G/T]CTGTGCATGCCCGCA | 11252 |
| rs568073301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935388 | GAAGGCTCTCCTGCA[C/T]AGACTGCCCCTCTTC | 11252 |
| rs568078397 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977940 | CAGTCTCAGGTGGTT[C/T]TTTATAGCAATGTGA | 11252 |
| rs568099780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000931 | AGGCCCTGCTTTTGC[A/G]TGACTCTCAGGCAAG | 11252 |
| rs568109516 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952918 | TGATCCACTGGCCTC[A/G]GCCTCCCACAGTGTT | 11252 |
| rs568111120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946688 | AGGATCCCTTCACAC[A/G]GGCATGCGCACACAC | 11252 |
| rs568141430 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909808 | CTGTAATAGCACTAT[A/C]TTTAGCTACATAATT | 11252 |
| rs568145021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002987 | TCCAGATCTCTCCCA[G/T]CTACAAACTGGATGG | 11252 |
| rs568166550 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924826 | CAGTGGCACGATCTC[A/G]GATCACTGCAAGCTC | 11252 |
| rs568174369 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977403 | AGAAGAAAAAATAAA[-/G]AAAAAAGGTGAAATG | 11252 |
| rs568179566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978628 | ACGGTAAGTTGTGGG[A/G]GGCAGTCGGGCAACA | 11252 |
| rs568187869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986340 | GGCTGTTTGGAAAAG[C/T]GCAGCGGCCCCCAAA | 11252 |
| rs568197543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941468 | GAGTTTCCAACATTC[A/T]GCCAGAGTGCTTTCC | 11252 |
| rs568199318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923862 | GGCAAGATGGTGAGA[A/T]CCCATCTCTAAAATA | 11252 |
| rs568202252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978005 | AGTACAAGTCTGAAA[A/G]AGACTAGAGCAATTC | 11252 |
| rs568216950 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970138 | CAAGCAGAGCAGGGT[-/C]CTGGCCTGAAGGGAT | 11252 |
| rs568220385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893150 | AAGCGGCAAGGCCTT[A/C]CACGTGATAGGAACT | 11252 |
| rs568266814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892522 | TCAAGCTCTGACTGA[C/T]AGCTTGATCCTGGGA | 11252 |
| rs568268179 | snp | A/G/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873053 | AACACCGCAAGAGAC[A/G/T]TAAGTCAAGCCACAC | 11252 |
| rs568277955 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971776 | GTAGCCCCCGCCCGG[C/G]CAGCCGCCCCATCCG | 11252 |
| rs568282823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935001 | GCTCACTGCAAGCTC[C/T]ACCTCCCAGGTTCAC | 11252 |
| rs568325573 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902670 | TGGTGCATCTCAGCA[A/G]TGGCATGATCTCGGC | 11252 |
| rs568338359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012454 | TGTTGGTGGAAATCC[A/G]GAATTTTTTTTAAAT | 11252 |
| rs568357138 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870844 | GGAATAGGGAGATCG[C/T]TTCCTCAAGACTGGT | 11252 |
| rs568382208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012088 | AGGCAGAGGTTACAG[C/T]GAGCTGAGATCGCAC | 11252 |
| rs568416953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006154 | CTGTCATGTGAAGCT[A/C]TAAGAAGTCAGCAAT | 11252 |
| rs568428629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961002 | GAAGATACACATGCA[C/T]ACTCCCCCATTCCCC | 11252 |
| rs568438519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942752 | TTGTTTTCTTGACTC[G/T]ATCTCATTTTTCCAT | 11252 |
| rs568445793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960507 | ACGCAACTGTGATTA[C/T]ATGGAAATAAAAACA | 11252 |
| rs568449175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006988 | TGGCAATCCTTGAGA[C/T]TCCCAGAGACAGAGG | 11252 |
| rs568480090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926340 | CCATCGGCCTGGGCA[G/T]GGTGGGGCAGAACAC | 11252 |
| rs568488281 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870366 | GCCAGACGTGTGCCT[A/G]AATGCCACAGACTTC | 11252 |
| rs568503327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880536 | AGGAGCCTAGCGGGG[A/G]CAGCACACCCACCCA | 11252 |
| rs568506030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917840 | ATGTTGCCCCGGCTG[A/G]CCTTTAACTCCTGGG | 11252 |
| rs568518124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911244 | CAAGAAAGCTCCAGG[C/G]GTTTTGCCACAGGGA | 11252 |
| rs568523181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917186 | TGGGGCATACAAAGG[A/G]TTGGAGCTTGCCCAA | 11252 |
| rs568540336 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880818 | CTCCCCACTGTGCCC[C/T]TCTTTGGGTATAATG | 11252 |
| rs568549955 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869601 | ACCCCAAGGGGCTCA[A/G]GTGCCTCAAATCCCC | 11252 |
| rs568554383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999274 | GCAAACCAGCCACAC[C/T]CCTGTCCCAAGTACC | 11252 |
| rs568609402 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870168 | CACAAGTAACACGAC[A/G]ACTGAAATCTGCAAC | 11252 |
| rs568658195 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995710 | TAATGTCCACCAGAC[A/C]GAGGCCTTAAAGCAC | 11252 |
| rs568661476 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987688 | AGGTGCGCACCACCA[C/T]ACCCGGCTAATTTTT | 11252 |
| rs568671515 | in-del | -/GG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904779 | CTGCACCCGAATCCT[-/GG]GGTTTACTTTATGAC | 11252 |
| rs568688122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957695 | AGTTCAGCTCAAGAC[A/G]GAGTCAGTATTCCCT | 11252 |
| rs568754804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935984 | TTTGGGAGGCCGAGG[C/T]GGGTGAATCACAAGG | 11252 |
| rs568759983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951315 | CAAAGCACCCAATTG[A/G]TGCCCTTATCACCCT | 11252 |
| rs568760070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929350 | AAAGGGAAAGTCAAC[A/G]GCAATTAATATTTGT | 11252 |
| rs568783831 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008938 | CAAAACACTCAAGCC[C/G]TACAAACTGTCCCTA | 11252 |
| rs568813364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900097 | TCCCTGATGCAGCCC[A/G]TCCTTGCTGGAGCAC | 11252 |
| rs568815423 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905824 | CTGGCCAGGGCTGGT[A/C]CCTGCCCTGTTTGCC | 11252 |
| rs568828841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877844 | CTTCTACTTCCAAGA[C/T]CAGGGCCTCAGGGCA | 11252 |
| rs568832740 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995816 | CACCTGTAATCCCAG[C/T]GCTCTGGGAAGCCGG | 11252 |
| rs568838403 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969889 | GCCTGAGTGACAGGG[G/T]GAGATGCTGGCCCTT | 11252 |
| rs568840911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920276 | GAACTCACTCTCACG[A/G]GCTACCCTGGGTGCC | 11252 |
| rs568857140 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015325 | ACGCGCATTGGTGAC[C/T]TCTCCTGTCAATCAA | 11252 |
| rs568857851 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011920 | GGGAGGCCAAGGCAG[G/T]TGGATCACAAGGTCA | 11252 |
| rs568868349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889790 | CCAACTAGCCAAGGC[C/T]CGACAAAACTCAATG | 11252 |
| rs568869466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871806 | CAGGAATCGTCCCTC[A/G]GTTGTGCCCCTCCCT | 11252 |
| rs568897329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963709 | AATAAGGGCAGAATG[C/G]GATTCAGTCAGGTCC | 11252 |
| rs568902324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913451 | GCCATTGCACTCCAG[C/T]CTGGGCAACAAGAGC | 11252 |
| rs568903943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882923 | GGGCCTCGGTTTCCT[C/T]CTCCGTTGAGTGGGC | 11252 |
| rs568974487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920702 | CAGTGCTGGAGACAG[A/G]CCTTGGCAGGGTAGG | 11252 |
| rs569035334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977106 | AATAGACACATATTA[C/T]ATTCATATGAGACTG | 11252 |
| rs569039371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970692 | TTTTAAAATTTAGCC[A/G]AGGAAGATGAAGCCT | 11252 |
| rs569078498 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872375 | TGGGCCTGCTGGCTC[A/G]GACCTCGTCAGGAGC | 11252 |
| rs569079175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938741 | CACCTGGAGCTCCAC[A/G]AGGGAAGGGCTTCAC | 11252 |
| rs569095501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984437 | GCCTCCCTGAAGCTT[C/T]CCTGATGTTGATATG | 11252 |
| rs569156136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880243 | TTAGGAAACTGAGGC[C/T]CAGAAAGGCAATGTG | 11252 |
| rs569156529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945772 | CCTAATCCTTAACAA[C/T]GTCCTAACTAACCTG | 11252 |
| rs569172031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991180 | TGCTGTACAATGGTA[C/T]AGACTTGGAGACTGC | 11252 |
| rs569177712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879495 | ACCAGGGCAAGGTCC[A/G]GGGCCTCCTGTTCCT | 11252 |
| rs569203551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908408 | GAAGCACTGGTGACA[C/T]GTGAAAAGCCCCAAG | 11252 |
| rs569209691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997950 | GTGTCTCAGAACACC[A/C]GTGACCACCGTTAGG | 11252 |
| rs569241411 | snp | A/G/T | 0.00676609 | 0.0577691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972065 | GGTTTTGTCCAATGG[A/G/T]GGGGGGAAATGTGGG | 11252 |
| rs569255345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897136 | GAGACAGGGTTTTGC[C/T]GTGTTGCCTAGGCTG | 11252 |
| rs569262019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978741 | AGTATGTTTGCATCC[C/T]GGCCCTTGGTTTATG | 11252 |
| rs569269786 | snp | C/T | 0 | 0 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939282 | CAAGCACCCTGGGAA[C/T]GTGGAGATGGAGGCT | 11252 |
| rs569322573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921683 | GGCTGCTATGAAAAG[A/G]GAGCAATCAGGAGCC | 11252 |
| rs569334299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893189 | TTCTGAGTTAACTCG[G/T]CAAGTGCAAGTGTGT | 11252 |
| rs569335286 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971425 | GCAGTGGCGTGATCT[C/T]GGCTCGCTACAACCC | 11252 |
| rs569338835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938253 | GAATAGAGAATGCTA[C/G]GCAGTGAATTCCTAA | 11252 |
| rs569343507 | in-del | -/CGGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971836 | GCCAGCAGCCCCGTC[-/CGGG]AGGGAGGTGGGGGGC | 11252 |
| rs569343737 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964411 | CGACAGAGCGAGACT[C/T]CGTCTGGAAAAAAAA | 11252 |
| rs569350082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891604 | ACGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGCT | 11252 |
| rs569371019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934145 | ACCAGCAAGTTGATC[C/T]GAATAACAACTTATA | 11252 |
| rs569410733 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016419 | TCTGGGAGGCCGAGG[C/T]GGGCAGATCACAAGG | 11252 |
| rs569439682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928329 | AAATATCACCTGCCA[C/T]CTTACACATGCATCA | 11252 |
| rs569440442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972564 | AAAAATAGTTCCTTA[C/T]ACATCTAGGAAAAAA | 11252 |
| rs569445863 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970507 | ATAAAATGTTAACAT[C/T]AGAGAAAGTCAGGCA | 11252 |
| rs569459384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010891 | TTTATTTGTTTTATG[C/T]GTGCTTTTCATCAAA | 11252 |
| rs569509342 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898684 | GAATCCACTCCCTTC[C/T]CCATGCCCTTCCCCG | 11252 |
| rs569512524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887288 | CCCTTGCTACACCGA[C/T]GGCATAGCAGTGAGG | 11252 |
| rs569521430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004762 | CAGTTGATCCTATCT[A/G]AAGACCACCCTGCAG | 11252 |
| rs569549371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888046 | TGCAGTCCCTCCCCC[A/G]GGTCTCTGCCCCCAG | 11252 |
| rs569574985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900012 | ACGGTTATTGATGAG[C/T]GAGTCCCCCTCCTAC | 11252 |
| rs569575026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942160 | CAGGGTCTCATGTTG[C/G]TCAGGCTGGTCTCAA | 11252 |
| rs569576453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915903 | TCCGAAGCCCTAAGG[C/T]GACACTGAGGCAAGA | 11252 |
| rs569585978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881600 | AGTGACCAATCCAAG[A/G]GCTAGGTGAGTCCTG | 11252 |
| rs569590352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905564 | GCTGAGCCTGACCTG[C/T]GACGGTGCACCCCAA | 11252 |
| rs569605074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007573 | CCTTCACGTCAGCCC[C/G]ACCTGGAGAGCACCT | 11252 |
| rs569617155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000893 | CTTACAGGTGGTCAG[A/G]AGTACCCCTCTGGAG | 11252 |
| rs569655990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905253 | GGAAGACAGGTCTGT[C/G]TGCACAACAGAAGGA | 11252 |
| rs569696771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935406 | ACTGCCCCTCTTCCA[C/T]ATGTGCGGAGACCTA | 11252 |
| rs569705077 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968825 | GCCAGCCTTTGGACT[C/T]CTGGACTTATACCAG | 11252 |
| rs569736374 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013779 | GTTTCCTGATTTTCA[C/T]CAAGACAGCCAGGCA | 11252 |
| rs569747102 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965431 | TAAAGAGGAAGAAGG[C/T]GGGAGAAGGAGGGGA | 11252 |
| rs569751599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967746 | ACAAAAAATTAGCCG[G/T]GCGTGGGGGTGGGCG | 11252 |
| rs569755031 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900751 | AGTGCTGGGATTACA[A/G]GCATGAGCCACCGCA | 11252 |
| rs569767608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012645 | GTGTGCACCACTACG[C/T]CAGACTAATTTTTTT | 11252 |
| rs569772300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930781 | ATGAAGAAACAGAGG[C/T]ATAAGAGTGTTTAAA | 11252 |
| rs569802034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924028 | ATCTGGGTGACAAAG[C/T]GAGACCTGGTCTCTT | 11252 |
| rs569808217 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968251 | TCACTGTTGTTGTTT[C/T]GGGGAAGGCAAAGGA | 11252 |
| rs569813516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961697 | AGAATCGCTTGACCC[C/T]AGGGAGCAGAGGTTG | 11252 |
| rs569820768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967398 | TGCCCCCTAAGGACA[C/T]TTAAAAAAGAAAAAG | 11252 |
| rs569830915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894244 | AGGCTGGAGCTGAAG[A/G]CAATTGTTTTTTTTT | 11252 |
| rs569848235 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015556 | AGTTTCCTCTCCCAA[A/G]GGACTCAAAGAAGCT | 11252 |
| rs569852058 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890062 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 11252 |
| rs569859919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876450 | CTGAGGGCTCCTTCC[C/G]AAGGAGCACAGGTGG | 11252 |
| rs569865604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881146 | CAGGGCCCACACTGT[C/T]ATTTGGAAAAACCTT | 11252 |
| rs569904766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876045 | CAAGTGAAACTAGCA[A/T]GAACTTTTCCAGACT | 11252 |
| rs569948040 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920599 | AGCTGTAACAACGCA[A/G]AAACAAGGCCGCACC | 11252 |
| rs569960656 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939064 | GCAGCAAAGGTAGGA[C/T]AGGCCCCAAGGTCAC | 11252 |
| rs569985649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919329 | ATTAAGAGGCTCGGG[A/G]CGACAGCTGTGAAAG | 11252 |
| rs569987646 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958650 | GTCGGACAGACATAC[C/T]ATATACCTTGGGGGT | 11252 |
| rs569995571 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870723 | GAGCATTCCCAATAG[A/G]AACCCGACCATAACC | 11252 |
| rs569997893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994351 | CCAAACACACCCAGA[A/C]AATAAGCATGAACTT | 11252 |
| rs570018408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932449 | AGACAGTGAATTCCA[A/G]AAGCGTATCTCACAT | 11252 |
| rs570021543 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870913 | AGGTGTATAAAAAAG[G/T]ATAACTGTACACAGC | 11252 |
| rs570031184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994807 | AGGTCTGGGGGCTGC[A/G]GGGAGCACCCTAGCA | 11252 |
| rs570038240 | in-del | -/TT | 0.450231 | 0.149691 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910909 | TCAGTTAACACATAA[-/TT]TTTTTTTTTTTTTGA | 11252 |
| rs570046741 | snp | A/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992723 | GGAAACAGCCCAAAC[A/G/T]TCTGTCAATAGGTGA | 11252 |
| rs570062150 | snp | A/G | 6.63053e-05 | 0.00575745 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876856 | AGACAGAGTGAGCGC[A/G]GTGGGAGCAGAGGAA | 11252 |
| rs570074529 | snp | C/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926232 | GAAACAGCTTGCGCA[C/G/T]TGCAAGATGCTTGGG | 11252 |
| rs570095043 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942956 | GATTTTGAAAGGGAC[C/T]GCTGTGACTCTGTAG | 11252 |
| rs570102328 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955787 | CCTATAGATGGGAAA[C/G]TAGTAACAAATGTTT | 11252 |
| rs570108921 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917486 | CAAGCATGGTGGCAC[A/G]CACCTGTGGTCCCAG | 11252 |
| rs570114361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949162 | TAAATAATAGGTGCA[C/T]ATTTTAACTTCTAAG | 11252 |
| rs570127588 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908749 | CAGCACTCTGTAAGA[C/T]CACACTCATTCAGGC | 11252 |
| rs570179192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895029 | GAATCCTGGTGAAAA[A/G]CAAAGACCCCTGGAA | 11252 |
| rs570239441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909445 | GGAAGATGTGCAGTT[A/G]GCAGTGTGCACCTGA | 11252 |
| rs570271486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892332 | CTGAGGGGAGGGCAG[A/G]CTGTGAGAACCCAGA | 11252 |
| rs570276643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974506 | AAGTACCACATACAG[A/G]CTTCTTGTCTGGGTA | 11252 |
| rs570280745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983379 | CTTCTAATCCCAGCT[A/G]CTTGGGAGGCTGAGG | 11252 |
| rs570290246 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014539 | TTCCCTCCAGCGTTG[C/T]TCCGGCACCCTCGCC | 11252 |
| rs570291500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895588 | GTTGGTACCACCCAT[C/T]GGCACACACAGGAGC | 11252 |
| rs570317773 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970049 | GAACCCAAATGCATC[C/T]CCACCTGACCTGGCA | 11252 |
| rs570319205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938094 | GACTGCCATTTAAGT[C/T]GAGCAAAATTTAAAA | 11252 |
| rs570320649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997542 | CAGCCTGGGCGACAG[C/T]GAGACTCCGTCTCAA | 11252 |
| rs570326234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889223 | CATGGAACACGCACA[G/T]GGAGGGGTTATGGGC | 11252 |
| rs570356082 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869694 | TCTTGCCCAGCTCCA[A/G]AGCTAGTAAGCCCCA | 11252 |
| rs570390171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974887 | TAAGCTTTGGGAATT[A/G]GTCCTCTTTTCCTTT | 11252 |
| rs570392857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952160 | ATGCACCAGGATTTT[A/G]CCTTGTTTGCCCGTG | 11252 |
| rs570419736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934982 | GTGCAGTGGCGCAAT[A/C]TCGGCTCACTGCAAG | 11252 |
| rs570431044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991428 | ATCCAGGCACAGAAG[C/G]CTTCTTCTCCCTCCA | 11252 |
| rs570448529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958586 | GGATCTGAAGAAAGA[C/G]ATATTCAGAGCTACA | 11252 |
| rs570466596 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946778 | TCATCTCTGCCACCA[C/G]TTCCCTCGCTTCTGG | 11252 |
| rs570476228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929163 | CTCACCAGGACCCCA[A/G]TGTCCGGGCTTGAGC | 11252 |
| rs570491344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873122 | AACACAGAAAATAGA[A/G]CGGACAGGAAAGCTT | 11252 |
| rs570499999 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901472 | CCTTCCCTTCACCTG[C/T]TCTCATGAGGGGAGC | 11252 |
| rs570509997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959160 | GAGGGGTCCTGGAGC[A/G]GTGGCAGGTGATCAG | 11252 |
| rs570541732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946611 | ACAGCAAGAAGCCCC[A/G]GTTACACAACACACA | 11252 |
| rs570557433 | in-del | -/TCTCCC | 0.00359209 | 0.0422272 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971093 | CCATGATAAAAATAT[-/TCTCCC]TCTCCCTCTCCCTCT | 11252 |
| rs570586509 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959841 | TGCAGCTCAGCTTCC[A/G]TACCTGCCTCTTTCC | 11252 |
| rs570625738 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886703 | GGATTTTGGAAACTG[C/T]GTCAAGAAGGGTGGT | 11252 |
| rs570648485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940625 | GGGCCACCCCAGGTC[A/C]TGGGTTTCCCTATAC | 11252 |
| rs570649162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898215 | GACAGGTTTCTCTGC[A/G]TACAGCACCCCTGCC | 11252 |
| rs570680892 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971287 | AGACGGGGTTTCGCC[C/G]TGTTGGCCGGGCTGG | 11252 |
| rs570720341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891883 | TCTCCTGGCATGGCT[C/G]CTATCAGCCCTGCTT | 11252 |
| rs570734753 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898942 | ACAGGCGTGCTGGGG[A/G]GACTATCCAAAGAGG | 11252 |
| rs570748836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953748 | ACCGGCTAGTTTTGA[A/C]ATTAAGACAATCTGT | 11252 |
| rs570760659 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893166 | CACGTGATAGGAACT[C/T]ACCCGAGTTCTGAGT | 11252 |
| rs570764763 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015802 | CTTGAAGGAAAATGG[A/G]GAGCACTTCCTGAGC | 11252 |
| rs570778741 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869507 | TGCTGTTTGGGCTGG[A/G]GCAATAGAGAGGCGC | 11252 |
| rs570794204 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977960 | TAGCAATGTGAGAAC[A/G]AACTAATACAGGGGT | 11252 |
| rs570815115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012014 | GCCAGGCGTGGTGGT[A/G]GATGCCTGTAGTCCC | 11252 |
| rs570822407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971699 | CCTCCGCCGGGCAGC[C/T]GCCCTGTCTGGGAAG | 11252 |
| rs570831570 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966384 | AAAAAAAAGCCACTT[G/T]TCTTTACTCATCCAA | 11252 |
| rs570836384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966040 | TTGCAAATCCTACTT[C/G]TTAGCCTTTCATATG | 11252 |
| rs570836892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892419 | CCTCTCTGTGCCTTC[A/G]TGTCTACAAAATGAG | 11252 |
| rs570909259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917159 | CCATGGGCATTGTCA[A/C]AGCAAGGAACCTGGG | 11252 |
| rs570948134 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880511 | GCAGCGCAGCCTCAG[C/G]TGAACTGCTAGGAGC | 11252 |
| rs570954482 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966386 | AAAAAAGCCACTTGT[A/C]TTTACTCATCCAACA | 11252 |
| rs570961460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998725 | AGCCTGGACCCAAGG[C/T]CCTAAATGAGAACAA | 11252 |
| rs571016081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874850 | TTGGCATTGGGCATC[C/T]GCTTTTTTTTTTTTT | 11252 |
| rs571022703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999195 | TGGGGCCAGAGCCCA[A/G]AAGTGCTCGCCTCGG | 11252 |
| rs571048988 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874342 | AAAAAAAAAAAAAAA[-/G]ATTATCATTGAAGAC | 11252 |
| rs571070710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910634 | AGATGTGGCTGGCGA[C/T]CTGTTTGGCTGTCAC | 11252 |
| rs571075635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947744 | TCTGCGCCTGACACT[A/G]CTCATGGGTAAAATA | 11252 |
| rs571081524 | in-del | -/TCTAA | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870503 | ACTGAGACATGACAG[-/TCTAA]TCTAAAGCATCTTTA | 11252 |
| rs571127471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993813 | GGGACAGCCATGTGC[A/G]CTGTGGGACCCAGAC | 11252 |
| rs571128438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939747 | TCCTGCCAGCCTGTT[C/T]CCTTACCTACAAGAG | 11252 |
| rs571137177 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871204 | TGCCGAGTCCCAGGC[A/G]AAATGACCAGCTCAT | 11252 |
| rs571144814 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977618 | TATGGTTAGGCTCTG[C/T]GTCCTCACCCAAATC | 11252 |
| rs571155419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956476 | TCAAAAGTAATCACT[A/G]TGGAAAAGCAAACAA | 11252 |
| rs571164545 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964180 | CCCAGTACTTTGTGG[A/G]GCCAAGGTGCGCAGA | 11252 |
| rs571166376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968597 | TAGTAAAGCCTGATT[C/T]TGGGGTGTGTCCATG | 11252 |
| rs571171282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904719 | TGGTGCTTCCACAGC[C/T]CCCCCATACTGCACT | 11252 |
| rs571173575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871750 | GACTGCGGCATCCAG[C/T]TCCATAGGGCTGTGC | 11252 |
| rs571187755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911195 | AGACATGAGCCACTG[C/T]GCCCGGCCATGCAAA | 11252 |
| rs571231093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925723 | CTAATGGTTAGAATT[A/C]TTTCGTAAACACTAC | 11252 |
| rs571239554 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894879 | CCTTGTCAGTTTTAC[A/C]TTTTCTAAAATCTCT | 11252 |
| rs571267102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990601 | TTCAGCAGGCAAAGA[C/T]GGGAAGAATGGCATT | 11252 |
| rs571276460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889155 | TGAGACGGAGCATGG[G/T]GTGGGTGGAGAAAGC | 11252 |
| rs571295219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968939 | CTGAGCCCCACTACC[A/G]GCATCCCAGAGTCTC | 11252 |
| rs571319998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008399 | GGGATTACAGGCACG[C/T]ACCACCATGACCAGC | 11252 |
| rs571323967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002246 | AAGAACCCTGCAGAG[C/T]CTTTCCAATATGCAT | 11252 |
| rs571404770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919583 | TTTAAGACCAGCCTG[G/T]CCAACATGGTGAAAC | 11252 |
| rs571407486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882784 | TGGGGGCTGCCTTCC[A/G]CCTGGCAGCCATCAT | 11252 |
| rs571409090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008893 | CATTTTAATGTACTC[G/T]TTCATCAATAAGCAT | 11252 |
| rs571417939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912593 | CGCCACTGAAGCCAC[A/C]AATTCAGACCAGTTT | 11252 |
| rs571433883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995671 | CAACAGTAAATATAC[A/G]GATTTGGTAACTTCA | 11252 |
| rs571445662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877717 | GGAGCTGAGTTACAC[A/G]CTACGAAGACCACAG | 11252 |
| rs571506028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976413 | ACTGGCCAGCCCAGG[C/T]GACAGACTGGCTCCT | 11252 |
| rs571528299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009936 | GTGCAGTGGCACAAT[C/T]TCGGCTCACTGCAGC | 11252 |
| rs571552935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913340 | CAAAATTAGCCAAGC[A/G]TGGTGGCATGTGCCT | 11252 |
| rs571557205 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989466 | TCACACGATTGCACT[A/C]CAGCCTGGGCAATAA | 11252 |
| rs571566247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010491 | GAGGCGGGCAGATCA[C/T]GAAGGTCAGGAGATC | 11252 |
| rs571612330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004189 | AGCTCTGATGGTGAC[C/T]CTCTGAAGGCCACTG | 11252 |
| rs571644285 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945125 | AAGAGGCAAGGGCTG[G/T]GTCATCTCCGTATCC | 11252 |
| rs571671751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898428 | AGACATGCGCCACCA[C/T]GCCCAGCTAATTTTG | 11252 |
| rs571672407 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888987 | ATTCATGGAGTACTT[G/T]CTTGTCCTGTGCATG | 11252 |
| rs571684921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975799 | CCAGGCATTTATTAG[C/T]ATGTTCCAAAACTTA | 11252 |
| rs571713014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927049 | TCCAAATGTTGGCTA[C/G]CACAGAGCTGTCAAG | 11252 |
| rs571714299 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890883 | CTAGGTGCAGGAGGT[A/G]GTGCTGCTAGTGGGG | 11252 |
| rs571718690 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958089 | TATGAACGGACTCAT[C/G]AGTAGAAAAAAAAAA | 11252 |
| rs571735088 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935171 | ACCTCATGATCTGCC[C/T]GTCTCGGCCTCCCAA | 11252 |
| rs571744782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970067 | ACCTGACCTGGCATG[C/T]CCCCTTCGACACTGG | 11252 |
| rs571773535 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920834 | TTGAGACAGGGTCTC[A/G]GTCTGCCGCCCAGGC | 11252 |
| rs571773879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933576 | ACTCCTCCCAAGCAA[A/C]AGCAGCAGCCTGTCC | 11252 |
| rs571794089 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993167 | AACAGAACAAGACTC[C/T]ATCTCAAAAAAAAAA | 11252 |
| rs571802882 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017406 | CTCGCCATGTTGCCC[A/G]GGCTCGTCTTGAACT | 11252 |
| rs571836967 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933978 | CCGGATACTCAAATA[A/C]CAGTGAAAAGCTACA | 11252 |
| rs571848603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892613 | TATCCTAGGCCCCTC[C/T]TCTGCCACGTGCCTG | 11252 |
| rs571849582 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922766 | TCTAAGCTGGGGGAG[C/G]GGCAGTGGACAAGGC | 11252 |
| rs571864360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884265 | AGGAGGCCCTGAGGG[C/T]GGTGAGGAGACCTCC | 11252 |
| rs571882153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963903 | ATACTATACTGCCTT[A/T]AAAAAAAAACAGCTT | 11252 |
| rs571942837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964371 | TGCAGTGAGCCAAGA[C/T]CGTGCCATTACACTC | 11252 |
| rs571948010 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921554 | CCCTTTCATAAAGTT[A/C]AAACTGAAATCAGGG | 11252 |
| rs571970871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978022 | GACTAGAGCAATTCA[A/G]TGTGACATAACTACT | 11252 |
| rs571984454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916946 | TGTTTTCCTGTCATT[G/T]TTGCTACTGGGATAA | 11252 |
| rs572002804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006289 | AGCCACCGCATCTTT[A/G]TTATAGCAGCCCCAA | 11252 |
| rs572007423 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014280 | CCTGCTTGGCCCCAG[A/C]CCTAGGACGTGCTGC | 11252 |
| rs572020967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917291 | GTGCTGAGTTCAAAT[A/C]TTCTAGAACATATAA | 11252 |
| rs572031649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971445 | CGCTACAACCCCCAC[C/T]TCCCAGCCGCCTGCC | 11252 |
| rs572035991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934687 | TGACCCTTTGCCCAC[C/T]ACTGTCCCGTTATAG | 11252 |
| rs572038202 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935011 | AGCTCCACCTCCCAG[G/T]TTCACGCCATTCTCC | 11252 |
| rs572069644 | in-del | -/AATG | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992635 | AGAGACTGGCACACA[-/AATG]TTAATAGCACCTTAT | 11252 |
| rs572082627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971821 | GGCAGCCCCCGCCCG[C/G]CCAGCAGCCCCGTCC | 11252 |
| rs572163096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941879 | ACTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 11252 |
| rs572206365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965624 | TGTCATTTTAGCCCA[A/C]GTGTATTTCTTGGGC | 11252 |
| rs572221486 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935944 | TCCAGCAGGGCACGG[C/T]GGCTCACGCCTGTAA | 11252 |
| rs572226214 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942341 | TTGATAACATCCTCT[G/T]AAGCACAAAAGTTCT | 11252 |
| rs572226310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935604 | CACAAATTATTCATC[A/G]AGTCCTATAATCACT | 11252 |
| rs572237439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005764 | GGCTCCTGGGGTCCA[C/T]CACCTCATGCTGCCC | 11252 |
| rs572258534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999351 | CTAATGTGTGTGTGT[A/G]TGTGTGTGTACGGAG | 11252 |
| rs572325851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910888 | TTGCCTAGCACACTA[C/T]AGGTACTCAGTTAAC | 11252 |
| rs572328197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953882 | AAAAAAGAGACGAAA[C/T]TCACCTAAGGAAAGC | 11252 |
| rs572342263 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960583 | ACAATAAAGCTTTAG[C/G]TGAGGAGAGAAAGAT | 11252 |
| rs572436210 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904912 | ACAATCGTTTATCCA[A/C]AAATGTCTCCATGGA | 11252 |
| rs572460073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875445 | TACAATCATGATTCA[C/T]TGCAACCTCAATCTA | 11252 |
| rs572500171 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869791 | ACGAGATCAACTGTT[C/T]ATTGATTTTTTTCCT | 11252 |
| rs572524709 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986838 | TTTTCTACCCATTCT[-/A]AAAAAAACCTTCCCG | 11252 |
| rs572539404 | in-del | -/TCAT | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956493 | GAAAAGCAAACAATG[-/TCAT]TCATTCATTCATTCA | 11252 |
| rs572548110 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978997 | TGGTGACCTCAGAAC[G/T]CTGACCAGTATAATG | 11252 |
| rs572558900 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909804 | AATTCTGTAATAGCA[C/T]TATATTTAGCTACAT | 11252 |
| rs572574844 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972996 | TGTGAGGATTGTTCA[C/T]TGTGAACCAGATTTA | 11252 |
| rs572602708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886980 | TCTCTCACACAGGCA[C/T]GCCCCCGCCCAACAT | 11252 |
| rs572617457 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987698 | CACCACACCCGGCTA[A/G]TTTTTTGTATTTTTA | 11252 |
| rs572626894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930393 | AGCACCTTTGTCTCA[C/G]CTCTCAGACCTTCTC | 11252 |
| rs572630067 | in-del | -/AAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956035 | CCTGTTAATTACATC[-/AAAA]AACATTTCGTCAAGT | 11252 |
| rs572638589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979564 | AGAAAAGAAAAAAGA[A/G]ATATACAGATATTTA | 11252 |
| rs572639073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900253 | CTTCGGGTCACAGCT[C/T]GTCTCAAAATTGCCT | 11252 |
| rs572642892 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884610 | ATTTCCATTTAGCCC[C/T]TGGCTCACCCTGCCC | 11252 |
| rs572660529 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006376 | GTCACCTAGTGATGG[A/C]GCTCGAACCCACACC | 11252 |
| rs572676451 | in-del | -/TTAAT | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915676 | TTATATACATCTTTA[-/TTAAT]TTAAGTAAAACAGAA | 11252 |
| rs572679185 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001678 | AGTCAAGTCTCTTCA[C/T]TTTGTTGTGAACATC | 11252 |
| rs572680531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893778 | GTAGTTAGATAATGA[A/G]CCTCTCTATTTTTAT | 11252 |
| rs572689290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887586 | TCCTCTCCAAACACC[A/G]AGGCAGGGCAGGCCC | 11252 |
| rs572746846 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938755 | CGAGGGAAGGGCTTC[A/C]CCCTTTTTATCTAAC | 11252 |
| rs572807654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013209 | TCAAATGAGTTGTTA[C/T]TCTTCTCCCAAAAAG | 11252 |
| rs572834422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970222 | GACTAAAGTAAACCC[A/G]CAAGGTTAACATCAC | 11252 |
| rs572843810 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933074 | TTTGAAAACACCTGG[C/T]AAAGCCAAGTTCCCA | 11252 |
| rs572864906 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877890 | CTGGATGGACTGCTC[A/T]GCCTGAGCACCCACC | 11252 |
| rs572867015 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903009 | AGCCAGTAACTTCAT[A/G]GCCGGCAGAAGAGCA | 11252 |
| rs572867441 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876712 | CCGAGGAATGGGGGT[A/G]CCAGAGAGCCTGTGC | 11252 |
| rs572896659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984106 | CTCCTGAGCAGCTGG[A/G]ATCATAGGTGTGCAC | 11252 |
| rs572910415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964507 | AGATTGCAGTTCTGC[A/G]CTCGCCTCAGTCTTT | 11252 |
| rs572912901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975362 | GGTGGCTCATGCCTA[C/T]AATCCCAGCACTTTG | 11252 |
| rs572916111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878820 | ATCTGTCAGCAGCTC[C/T]GGCACCAGGCAGGAA | 11252 |
| rs572952668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890159 | GGTGCCCGCCACCAC[A/G]CCCTGCTAATTTTTG | 11252 |
| rs572953264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872729 | CTGTGAAGATTAAGT[A/G]TTAAGACACTAAAGA | 11252 |
| rs573039203 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895925 | GTCTCTATCGCCATA[A/C]ACCACCAGGGACAGA | 11252 |
| rs573067876 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997485 | ATCGCTTGAACCCGG[C/G]AGGCAGAGGTTGCAG | 11252 |
| rs573073554 | in-del | -/T/TT | 0.415235 | 0.18761 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890004 | AGCAGCCAAAGGGAC[-/T/TT]TTTTTTTTTTTTTTT | 11252 |
| rs573095944 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003477 | GCGTGGTGGCGGGCA[C/G]CTGTAGTCCCAGCTA | 11252 |
| rs573104857 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984399 | CTCAATTTCCCACCC[A/G]GAAGAAATGCTCTAG | 11252 |
| rs573166611 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883876 | GGGTGTGGTGGCGCA[C/T]GCCTGTAATCCCAGC | 11252 |
| rs573167350 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015472 | GGCATCCAGGGGTAA[C/G]AGGGCGCGGCAGGGC | 11252 |
| rs573191421 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005062 | CTTAAACATTAATCT[-/A]AAAGTAAAAGGGCAA | 11252 |
| rs573205866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009973 | CTCCCGGGTTCTAGT[C/G]ATTCTCCTGCCTCAG | 11252 |
| rs573247234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985930 | GATGTCCATTACAGG[A/G]CCACTATAGAGCCAC | 11252 |
| rs573258813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958883 | TAAGTATCAGGATTT[A/T]AAAAATCTAATTAGA | 11252 |
| rs573293433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997758 | CCTGTGGTCCCAGCT[A/G]TTACTTCACTCGGGA | 11252 |
| rs573296996 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923940 | CCAGCTACTCAGGGG[G/T]CTGAGGCAGGGGAAC | 11252 |
| rs573317376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880641 | GTGGCATGAAAAATA[A/C]AAACAAAGAATTGCA | 11252 |
| rs573331860 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909873 | AGACAATGTCGCCAA[A/G]GGCACCGCAGGAACA | 11252 |
| rs573353984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875584 | TCTGTCACCCAGCCT[G/T]GGGTACAGTGGTGTG | 11252 |
| rs573362211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881230 | CTATGAGGCGCCCAG[A/G]AGGTTTCTGAGTGGT | 11252 |
| rs573372359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914421 | TATTTTTTAGTAGAG[A/T]TGGGGTTTCCACCAT | 11252 |
| rs573375533 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946114 | AATGAATTAGAGGAG[A/G]TGGAGGAGAAATCAA | 11252 |
| rs573400373 | snp | A/T | 0.119281 | 0.213102 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952667 | CCGGCCTATTTATTT[A/T]TTTTTTTTTTTTTGA | 11252 |
| rs573434424 | in-del | -/ACCGTAACTGCTTAA | 0.00636936 | 0.0560724 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974655 | TCGGGTGGCTGAGGC[-/ACCGTAACTGCTTAA]ACCTGGGAGGTGGAG | 11252 |
| rs573443366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909638 | TCAGGCAAAAGGAGA[C/T]GTTCTTGTCTACTGA | 11252 |
| rs573471196 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903197 | GGGCTCCAGGACTGA[C/G]TCCCTTCTCCTCAGG | 11252 |
| rs573476095 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993999 | ACAAGTTCCATAAGT[C/T]AACATTAAAAACTCT | 11252 |
| rs573490507 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970638 | ACGAACATTCATTAC[A/G]TCCTTTGCAAAAAGG | 11252 |
| rs573498518 | snp | G/T | 1.70229e-05 | 0.00291739 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876098 | ACAGCCTGCAGGTTG[G/T]AAGCCCTCCTCCCCT | 11252 |
| rs573512187 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948603 | TGATAGTGCCTGTGA[A/G]TAGCCACTGTACTCC | 11252 |
| rs573516917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946157 | AAATAGTTTCAAAAG[C/T]AAAATAATAAGAATC | 11252 |
| rs573533967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939872 | ATCTTGAGCACCTGC[A/G]ATGTTCCAGGAACAG | 11252 |
| rs573534012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946709 | GCGCACACACATGAT[C/T]CTCTCTCGTCCAGCT | 11252 |
| rs573535627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886801 | GCCAGACCAAAGAGG[C/T]AGGGAGGGTCCCAGG | 11252 |
| rs573537347 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990069 | ACACACATATGTGTG[-/TA]TATATATGTGTGTGT | 11252 |
| rs573585809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994415 | CAGAGCCGTGTCCTG[C/T]GCCACAAAGACCCTC | 11252 |
| rs573602679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887374 | CTGCTGGATGGCACG[G/T]GACTTAACCTCTCTG | 11252 |
| rs573612900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930925 | AGGCAACAAAAGACA[A/C]CAAGGAAAGGCAGAG | 11252 |
| rs573628078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900391 | ACTTGGCCAGGCAGG[G/T]TACTGACAGTTTTAC | 11252 |
| rs573634488 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954749 | GAAAGAGGAATATAT[A/C]CAAGAGGAAAAACAG | 11252 |
| rs573650840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007247 | TTTTTGAGACAGTCT[C/T]GCTCTGTCACCCAGG | 11252 |
| rs573664963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000256 | GACCCCAAAAGCCAG[C/T]CATCCTGGACAGCAG | 11252 |
| rs573678340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917654 | AAAGTGAACACGCAC[C/T]GCTCTGCGGTGTGCC | 11252 |
| rs573685387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961308 | TGTGTTTAGACAAAC[A/G]CTGCGGAAGGCCGCA | 11252 |
| rs573748724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954793 | ATGGATGATGCCAGG[A/G]AATGGGGGATGGGGG | 11252 |
| rs573786689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955402 | AACGGATGGCTGGAA[A/G]TAAGCCCAGAGCTCA | 11252 |
| rs573798820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976942 | TCCAGCCGACACAAT[A/G]CCTCATGTTATGCTA | 11252 |
| rs573818436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925251 | TTGGGCGGCCGAGGC[C/T]GGCGGATCACTTGAG | 11252 |
| rs573824518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014079 | TCGACCTTCTCTGAT[A/G]GAGCCGAAACCCAAT | 11252 |
| rs573836758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895129 | CCTCCCCCAGCAAGG[C/T]TGGCAGCTCGGCAGC | 11252 |
| rs573854507 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870740 | ACCCGACCATAACCC[A/G/T]GTCCCACCTTCCTGG | 11252 |
| rs573866785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987781 | CCTCATCATCTACCC[A/G]CCTCCGCCTCCCAAA | 11252 |
| rs573888377 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979473 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 11252 |
| rs573888629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948649 | GTGAGATCCCATCTC[A/T]AAAAAAAAATTTTAA | 11252 |
| rs573952539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949290 | CTCCAGCCTTCCCAG[C/G]CTTCTTGCTCCTAGT | 11252 |
| rs573954620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942585 | GAGTTAAGTTTTATA[C/T]GTGGCATGAGGCAGA | 11252 |
| rs573970407 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973899 | GCCTCATCCTTGGGG[A/G]CACATAGCTCAGGTG | 11252 |
| rs573991496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919729 | AGTGAGCCGAGATTG[C/T]ACCACTGTACTCCAG | 11252 |
| rs573996431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936920 | TGCCTCAAAAAAAGG[C/G]GGGGGGGCAGGGGCA | 11252 |
| rs574005491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920313 | GATGAATCAGAAGCA[C/T]GCCATCCGAATTCCA | 11252 |
| rs574037906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003953 | CTGCTGTGTAAATGG[C/T]TGTAAACTTTCAGAT | 11252 |
| rs574063730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903164 | CCTAAGCCAACCCAC[A/G]TCCCAGGCAGCTAGA | 11252 |
| rs574067062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943052 | TTTCCATTTATTCAG[G/T]TCCTTTTAAATTTAT | 11252 |
| rs574077419 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951939 | CCTTTGCACCTGCCT[C/T]CCCTCTGCCGGGAAT | 11252 |
| rs574103189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931982 | ACTTCCAGTTTCTAG[A/C]CTCTTCAGGGCAATA | 11252 |
| rs574179334 | in-del | -/TA | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947648 | TCTGAAATCTGCATC[-/TA]TGAGTCTTCACAAGA | 11252 |
| rs574184952 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016257 | AATTGCTGCTACATA[C/T]AGATAGGTATGAGAA | 11252 |
| rs574190430 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882407 | GGTCTCTGCCCTCTG[A/T]GAGTTGGTTTCACAG | 11252 |
| rs574191121 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42873932 | TAGCTGGGATTACAG[A/G]TGTGTGCCACCATGC | 11252 |
| rs574212189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928032 | ATGCAGCTTCCACTT[C/T]TGTCCCACTGTTTCC | 11252 |
| rs574219783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967993 | CTTTATATACAATGA[C/T]ATACTCAGGATATAC | 11252 |
| rs574220380 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016875 | TAGAGCCTTGTCGGG[C/T]GCTGTGGCTCACGCC | 11252 |
| rs574247728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001882 | CACTGCTCCCCACCT[A/G]GAGCCCCTCTCTGTC | 11252 |
| rs574257420 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903269 | GGGGAGGGTGTGCGT[C/G]TGCCTGGCAGATGTT | 11252 |
| rs574262733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912956 | GGTGAGACAGAATGG[C/T]CAACTTGTTTTGAGC | 11252 |
| rs574284335 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002375 | GGGAACGTGGAACAT[G/T]AGCTCCAAGGATTAA | 11252 |
| rs574292700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962720 | GGATGCCTGGGGTGG[A/G]TGGAGGCATTGTGAG | 11252 |
| rs574292783 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951570 | TGCTCCTGCATCCCC[A/C]GGTTGGGCTCCTCCA | 11252 |
| rs574306213 | in-del | -/T | 0.432651 | 0.170701 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873798 | AGCAATTTTCTTTCC[-/T]TTTTTTTTTTTTTGA | 11252 |
| rs574324222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928748 | ACACAAATACATATA[C/G]CTCTAAACAAACAAA | 11252 |
| rs574334738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938939 | CCCTTAAAATAACCA[C/T]GTTTTCCCCAACATC | 11252 |
| rs574336070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877279 | AGGGGCCCTGGGGTG[G/T]CCCAGGGGCGGGTGA | 11252 |
| rs574358327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963314 | CCATGTGGATTAAGG[C/T]GGAAGAAAATTCAGA | 11252 |
| rs574383120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897522 | TGCTTCATTCACAAA[A/G]TCCTCATTTTTGAAC | 11252 |
| rs574395996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995269 | CTGCTTCTGACATGA[A/C]GTGTGGCAAGCCTTA | 11252 |
| rs574410968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940272 | CAAAAATAGATTTTT[C/T]TATTTTATACAATAG | 11252 |
| rs574436105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934322 | CAGCACAATTTCTAC[A/G]GGAAACGCAAGACCT | 11252 |
| rs574470799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945999 | GGCCACACTATACAC[A/G]CTCTGGCCACCGTTA | 11252 |
| rs574488430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952733 | AGTGGAGCGATCTCG[C/G]CTCACTACAATCTCT | 11252 |
| rs574502557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964698 | CCAAACACAGAGCCA[C/G]GTGATCCATCGGCAG | 11252 |
| rs574520577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891444 | TCGCTCTTATTGTCC[C/T]GGCTGGAGTGCAGAG | 11252 |
| rs574527237 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003893 | GCGAGTCACCCACGG[C/T]CTTGACCGCACCCCA | 11252 |
| rs574579802 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899180 | TCCACAGGGTCTACC[A/G]CACAGCAGGCACCCC | 11252 |
| rs574595944 | in-del | -/TTTT | 0.00718984 | 0.059525 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973428 | ATCTGTACCACACTG[-/TTTT]TTGTCAACAAGGCTC | 11252 |
| rs574596692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011648 | CTGCGAGGCCGAGGC[A/G]GGCAGATCACTGGAG | 11252 |
| rs574627946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970947 | TGCACCACCCTGCCC[C/T]GCCCCCAGCCTCTCC | 11252 |
| rs574629308 | in-del | -/TTTA/TTTATTTA | 0.0229078 | 0.104636 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927555 | GCCTGGCCCCAGTCT[-/TTTA/TTTATTTA]TTTATTTATTTATTT | 11252 |
| rs574638536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971340 | GATCTGCCCGCCTCA[C/G]CCTCCCGAGGTGCCA | 11252 |
| rs574673833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966087 | GTAAATAGAGCCATC[C/T]TGGGCTGGGCGCGGT | 11252 |
| rs574674870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947836 | TGCCTGGAGTATGGG[A/G]ACCTTCCACAAGCAT | 11252 |
| rs574747180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909773 | CACCTGAATGTTTTT[C/T]AACAAGCAGCTGAAG | 11252 |
| rs574777418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874872 | TTTTTTTTTTTTGAA[A/G]AAGAGTTTTGCTCTG | 11252 |
| rs574821118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910327 | GGAAAGGTTTCTATC[C/T]ATAGTTTTGGTTCAG | 11252 |
| rs574858820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923233 | ACTGTTGCATGTCTT[C/T]TCAATGCATGATATA | 11252 |
| rs574860945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998803 | CCCCATCATCCTGTG[C/T]CCATATAAAACCCCA | 11252 |
| rs574885023 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003897 | GTCACCCACGGCCTT[C/G]ACCGCACCCCAGCAG | 11252 |
| rs574894598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986792 | AGCAGCTACTGCATC[A/G]ACACTTGTCTCTCTA | 11252 |
| rs574903201 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956091 | TCCTTGTTCTCCTTC[A/G]AGGACTCCACTGTAG | 11252 |
| rs574924157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986414 | CAAACGAAATCAAAC[A/G]CCTAAAAGAAATGAC | 11252 |
| rs574955835 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990915 | CAGCCCAAAGACTTC[C/T]TCCAGATGGTCACCT | 11252 |
| rs574971006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993023 | ACAAAAAAATTGGCC[A/G]GGCATGGCAGCATGC | 11252 |
| rs574978237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941793 | GTTTTGTTTGAGACA[A/G]AGTCTCACTCTGTCA | 11252 |
| rs574980705 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892890 | AAGTTCCCCTTCCCT[C/G]CTGGGAAGTGTGTTC | 11252 |
| rs574990275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935445 | ATGGCTCCAGACTCA[C/T]GGTCTTGTCTAGGGT | 11252 |
| rs574996611 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004706 | GTATCACTTTACATT[-/AAG]AAGATTTCATTTCAT | 11252 |
| rs575022914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935113 | TTTATTTTCAGTAGA[C/G]TCGGGGTTTCACTGT | 11252 |
| rs575054915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904744 | TGCACTCCAGTCTAC[C/T]TCCACCCTGGCCCTA | 11252 |
| rs575054977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898983 | TCCTCCTCCATCCTG[C/T]ATGCATCTGTTGTAA | 11252 |
| rs575057018 | in-del | -/AA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989860 | TTCTCTTGGAGGGGG[-/AA]AAAAAAATATATATA | 11252 |
| rs575071858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893234 | GGGCTATAGTCCTGT[G/T]TCCCCAAGGAAAGTG | 11252 |
| rs575091257 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899553 | AAAGGCCAAGTGTGG[A/G]CAGAGGTGGGTGTAC | 11252 |
| rs575105780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012237 | AGGCAAGGTGGCAGG[C/T]GCCTGTAATCCCAAC | 11252 |
| rs575111984 | in-del | -/AAAAAGG | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993179 | TCCATCTCAAAAAAA[-/AAAAAGG]AAAAAGGAAGAAGAA | 11252 |
| rs575125926 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876755 | AGTGGGCCAGGGTGC[A/G]GCACGCCAGGTGCCC | 11252 |
| rs575164644 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870858 | GTTTCCTCAAGACTG[A/G]TGCGCATCAATCTGT | 11252 |
| rs575167350 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962577 | CTGGGGGTGGGGGGT[G/T]GAGGGTGAGGTCTGG | 11252 |
| rs575209198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924849 | GCAAGCTCTGCCTCC[C/T]GGGTACACGCCATTC | 11252 |
| rs575211977 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973544 | ATCAGAAACTCTACA[C/T]ATACACTTTGGAATT | 11252 |
| rs575222374 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994575 | ACACGCCAGGGAGGC[A/G]GCCCATGCAGGCCAT | 11252 |
| rs575245400 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954105 | GTCTCTACCAAAAAA[C/T]TCAAAAAATTAGCCA | 11252 |
| rs575254252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970206 | ATTTAAAAAGGAGAA[C/T]GACTAAAGTAAACCC | 11252 |
| rs575281481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912304 | GTGGCAGAAAGCCAG[G/T]AGACTCTAATCAACT | 11252 |
| rs575295240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883872 | AGCTGGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 11252 |
| rs575305363 | snp | A/T | 1.69882e-05 | 0.00291441 | missense | PACSIN2 | GRCh38.p7 | 22:42882302 | TGGTAAATGGCTTTG[A/T]AGCTAAATCAGAGAG | 11252 |
| rs575308807 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983113 | CCTGAAGTCACGAGT[C/T]CGAGACCAGCCTGGC | 11252 |
| rs575336130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001836 | CTAGGGAGGGGACCC[A/G]GGGGTAAGCACTAAG | 11252 |
| rs575343213 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957937 | GGCAAGCAAAACTTT[A/G]TAATATAGAGAATTG | 11252 |
| rs575346653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003365 | TAATCCCAGCACTTC[A/G]GGAGGCCAAGGCAGG | 11252 |
| rs575397321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937856 | CAGACATGGAGCCCC[A/G]CAGGGGGACCCTTCT | 11252 |
| rs575398413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42995181 | GAGTTCTTCCTCTAT[A/G]AAGTGAGCTGACTGC | 11252 |
| rs575407148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996900 | ACAAAGTTGTCATGA[C/G]AATAAGTGTAATCAC | 11252 |
| rs575431133 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878707 | CCTCCACCAGTGTCC[C/G]GGCAGGGCGGTGCTA | 11252 |
| rs575474207 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917438 | ATAGTGAGATCCCAT[C/T]TCTACAAAAAGTAGA | 11252 |
| rs575474606 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884101 | ACCCAGACCTGTACA[A/T]GGAGTTGGCAGAGTG | 11252 |
| rs575514565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908034 | TGCCAACTCTTCAGG[G/T]CTAACATTCCCAGAA | 11252 |
| rs575518237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997629 | ACATTGAATTGCATG[C/T]AAAAATGTCTGAGTC | 11252 |
| rs575525343 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899276 | ACGGCATGGCTCCTT[A/G]AACAAAATTTTTCTT | 11252 |
| rs575531368 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945658 | TCAATCAGCTTCCAA[A/G]ACCGGACTACATCAG | 11252 |
| rs575538357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895889 | CGGTTGTGTGGTGGC[C/T]GGTGAAGGCCATCAC | 11252 |
| rs575562367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902690 | ATGATCTCGGCTCAC[C/T]ACAACCTCTGCCTCC | 11252 |
| rs575563760 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009568 | AGTCCTTCATTTTAC[A/G]AATATGAAAACTGAG | 11252 |
| rs575565823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963489 | TTCATCAGCCTAGCA[A/G]GACTCAAAGACAGGA | 11252 |
| rs575568256 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943827 | TATCAGAGGAAAACA[C/T]GAATGTGTCCAAAAC | 11252 |
| rs575611002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878048 | AATATCCAGGCCACA[C/T]GTCTGAGCTCACCGG | 11252 |
| rs575619285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892754 | TGGGACCTGGCTCCC[C/T]TGATTGGCTGAGGAC | 11252 |
| rs575644566 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009969 | CTGCCTCCCGGGTTC[A/T]AGTGATTCTCCTGCC | 11252 |
| rs575645932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972168 | CTGTGCTAGGAAAGA[C/T]TCTTCTGCCTTGGGA | 11252 |
| rs575678320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957092 | CTGAGCCTGCAGCCC[C/G]ACTTCTTCTCTAGGA | 11252 |
| rs575678572 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901785 | TGTCTGGTTGAAGAC[A/G]ATGTTGGTGCTTCCT | 11252 |
| rs575683356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005856 | CCCCTCAAAATTCAT[A/G]TGTTGAAATTCTACC | 11252 |
| rs575693532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886704 | GATTTTGGAAACTGC[A/G]TCAAGAAGGGTGGTG | 11252 |
| rs575744537 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933671 | CCACTCAAACCCCAA[C/G/T]GGGGCCCTCACAGCC | 11252 |
| rs575746981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006575 | ATCCCAGCACTTTGG[C/G]AGGCAGAGGCAGGCG | 11252 |
| rs575750340 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999668 | ATGAAACTCCATCTC[-/A]AAAAAAAAAAATGCT | 11252 |
| rs575764942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914308 | TGCAATCTCAGCTCA[C/G]TAAAACCTCTGCTTC | 11252 |
| rs575803584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927193 | GCCATCCTGTGTTCT[A/G]CTTTCCTCAGCTGCA | 11252 |
| rs575830829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872607 | GCTTCCAGTGCTCCC[C/T]GGACTGCCTGGGCTC | 11252 |
| rs575834508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990968 | TCTGTAAAATGGACA[A/G]CAGCCACCTCACAAC | 11252 |
| rs575857264 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903642 | ACTTCGGTGCTGCCT[G/T]GAACCACAAGCTCAG | 11252 |
| rs575868059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921825 | CTCACTGCAACCTCC[A/G]TCTCCCGGGTTCAGG | 11252 |
| rs575871003 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903080 | AGCACAGCCAGCTGC[A/C]GGGCCTCACCGGGCC | 11252 |
| rs575910789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910923 | AATTTTTTTTTTTTT[C/G]AGACGGAGTCTTGCT | 11252 |
| rs575918129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951597 | TCCAGGACACAGCTG[C/T]TCAGGACAAATGCCC | 11252 |
| rs575926133 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969050 | CTATCTATCTCCATC[C/T]ATCCATCCATCCATC | 11252 |
| rs575944445 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971912 | AGCCTCCACCCGGCC[A/G]CCGCCCCGTCTGGAA | 11252 |
| rs575964119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905003 | ATTTGTTACTGAATA[G/T]AAAGGAAAAATGTGT | 11252 |
| rs575966843 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017429 | CTTGAACTCCTGGGC[G/T]CAAGCAATCCTCCTG | 11252 |
| rs575973354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911487 | TCAGGAACAACACCC[A/T]CCGCCTCCACAAAAA | 11252 |
| rs575979325 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945455 | GTCTGGCCCAGACCC[C/G]CATCTCTGCCTACTG | 11252 |
| rs575998371 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905567 | GAGCCTGACCTGCGA[C/T]GGTGCACCCCAAATT | 11252 |
| rs576001432 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869658 | GCCGTGGCCTTTTGG[A/G]CAGGGGTCCTGTGCC | 11252 |
| rs576033543 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896064 | CTGCCCACTACAGGG[C/T]ACACTTAGATCTGAA | 11252 |
| rs576045671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880351 | CTGACCAAAATAGAT[C/T]GACTGAGAACTCAAT | 11252 |
| rs576055358 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012162 | ATAAATAAATACATA[A/C]ATACATACATACATA | 11252 |
| rs576055848 | in-del | -/ATGGGAGAA | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990636 | GTAGACAAGATTTGC[-/ATGGGAGAA]ATGCAAGAAGTTCAG | 11252 |
| rs576059498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923578 | GACTACAGGCGCCCG[C/T]CACCATGCCTGGCTA | 11252 |
| rs576071748 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929718 | GGACAAGGCAGGAGA[C/G]TGACCCGCCACCCGG | 11252 |
| rs576084162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966801 | GCAACACATTAAAAA[C/T]GGAAGATGATCCAAG | 11252 |
| rs576087605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936116 | AGCTACTCAGGAGGC[A/T]GAGGCAGGAGAATGG | 11252 |
| rs576105380 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002090 | ACAAGGCAAGCAAGC[A/G]CCAGTGCTATAAACT | 11252 |
| rs576152786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880600 | ACTCTATGAGGTAGC[C/T]GAACGCAGACACTTA | 11252 |
| rs576242590 | snp | C/T | 1.68411e-05 | 0.00290177 | missense | PACSIN2 | GRCh38.p7 | 22:42893475 | TCTCCACGAGCTGCC[C/T]CCAGCGCCGGGCCCA | 11252 |
| rs576261265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947954 | CATTCTCACAGGGTC[A/G]ATGGACACTTGAACA | 11252 |
| rs576262538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931492 | AGACAGAAGAGACCT[C/T]AGGTGATGGGAAGGT | 11252 |
| rs576273625 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993583 | GGTCAAAATTTTATA[A/C]AGAAAGAGCCCTTCC | 11252 |
| rs576287736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987015 | TCCATTCCCACTGAC[A/G]CCTTCCCTAACTAAC | 11252 |
| rs576315415 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953953 | GAGAGAATAAGAACA[G/T]CAAGTACAAAGGTTA | 11252 |
| rs576357293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899738 | CAGGACAGGTAGGGG[A/G]CCTCTCCCTGGGGAA | 11252 |
| rs576375072 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869911 | GGTAAGTTCTCAGGA[C/T]AGACACAGACACAGG | 11252 |
| rs576379259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954674 | GTTAGTGGCTACCAC[A/T]CTGGACATCGCAGTT | 11252 |
| rs576402576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907980 | ACAACCTACAGGGAG[C/G]GCCTTCCTGGCAGGG | 11252 |
| rs576481786 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938850 | GTGCTGGATCCCGAG[A/G]TGGAGAAGGTAAAAA | 11252 |
| rs576503577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936789 | GGCAGCACACATCTG[A/C]AATTCCAGCTACTCA | 11252 |
| rs576505117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893851 | TGTTCTTTAGGTTGG[A/G]TACCAAGTAGAAACT | 11252 |
| rs576534197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967610 | ACCCTGCAAATGGGC[C/T]GGGCGCGGTGGCTCA | 11252 |
| rs576548215 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894892 | ACCTTTTCTAAAATC[C/T]CTTTGCCTGGCCCTG | 11252 |
| rs576562608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894434 | TTTTAGTGGAGACAG[A/G]GTTTCACCATGTTGG | 11252 |
| rs576607032 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887427 | AACAGGGATGCCACC[A/G]CCTAACTGACAGGGG | 11252 |
| rs576655362 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925121 | TCTCCCAAGCACTTA[A/C]CACCTCCTAACGAGC | 11252 |
| rs576665871 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973786 | CTCCATCATCCCTCA[C/T]TGCCCTTGTTTCCTT | 11252 |
| rs576692436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887703 | TGAACTTTTAAATCA[C/T]AAGACGATGACGCTG | 11252 |
| rs576725752 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910332 | GGTTTCTATCTATAG[C/T]TTTGGTTCAGTGTTG | 11252 |
| rs576729389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888587 | AGGCTATATGCCAGA[C/T]ACGTCAACAACTGAC | 11252 |
| rs576736800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901974 | TCTGCTGATGCCACC[A/G]GCTGGCTGGCTCCCC | 11252 |
| rs576741925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990803 | AATAAGAACATGAAG[A/G]TGTGGAAGAGGGCCA | 11252 |
| rs576748428 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951483 | GATCCGGCATGGCCC[A/G]AGCTGCTGGCTCAGC | 11252 |
| rs576782947 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902556 | CTGAGAAGTCGCTGA[C/G]ATCTCAGAGGCATGG | 11252 |
| rs576794921 | in-del | -/T | 0.443059 | 0.158834 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973431 | TGTACCACACTGTTT[-/T]TTGTCAACAAGGCTC | 11252 |
| rs576811587 | snp | C/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873593 | GGTAAGGCAGCCTTT[C/T]CCACAAGTGTAGCCT | 11252 |
| rs576814946 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958971 | ACTTCTAAGAAACAA[C/T]TGAATACGTACATAA | 11252 |
| rs576820320 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999576 | TGGGAGGCTGAAGAA[A/G]AGAATCGCTTGAACC | 11252 |
| rs576822207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001062 | AACTTAGGCCAAGGG[C/T]TGCTATGGAATCACG | 11252 |
| rs576865452 | in-del | -/AAAAC/AAC | 0.208169 | 0.246476 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983499 | ATCTCAAAAAAAAAA[-/AAAAC/AAC]AAAAAAAAACAGATA | 11252 |
| rs576964317 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969500 | TGGGGAAGAACCAAA[C/T]ACATTTAAGATGAGT | 11252 |
| rs576992457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986052 | TGACTTTCCAAACAA[C/T]GATCCCCTTGCTCTG | 11252 |
| rs576993018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984651 | CTTCAGGGCATCTGG[C/G]AATAAGGAGCAGGGT | 11252 |
| rs577019271 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004732 | ATTTCATTCAATAGG[-/A]AACTTCAGAATACAC | 11252 |
| rs577027559 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017106 | GTGAGCTGATATCGC[A/G]CCACTGCACTCCAGC | 11252 |
| rs577050795 | in-del | -/A | 0.410905 | 0.191336 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996219 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAATAATA | 11252 |
| rs577054694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985273 | CAGAGGTTGCAGTGA[A/G]CCGAGATCTCATCAC | 11252 |
| rs577081849 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002834 | CATTACGTCAACAGG[A/G]TAATATAACCATTAA | 11252 |
| rs577099672 | snp | C/G | 5.00088e-05 | 0.00500019 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890895 | GGTGGTGCTGCTAGT[C/G]GGGTGCCAGGCAGAG | 11252 |
| rs577102917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986396 | GGGCAGCATTCATCC[A/G]GCCAAACGAAATCAA | 11252 |
| rs577111739 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920905 | CCTCCTCAGCTCAAG[C/T]GATCCTCCCACCTCG | 11252 |
| rs577113694 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894354 | CAAGTGATTCTTCTG[C/T]CTCAGCCTCCTCAGT | 11252 |
| rs577131142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922282 | GATAACAGATATCAG[C/G]TAAACAAATGATGTA | 11252 |
| rs577131627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883921 | AGGCAGGAGAACTGC[A/T]TGAAACCAGAAGGTG | 11252 |
| rs577155260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978152 | TTTTTTCAATTATTT[C/G]TTATCAAAAGAGCTT | 11252 |
| rs577159378 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014064 | CTTCTGAAAAGAAAA[G/T]CGACCTTCTCTGATG | 11252 |
| rs577168229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986632 | ATCCACATGGGAACA[C/T]AATGACTTCAGACAC | 11252 |
| rs577186242 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964973 | TCTGCCTTCCTCATA[G/T]GCTGCTGAAAGATGG | 11252 |
| rs577196191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997794 | AGTGAGGCAGGAGAA[C/T]CATCTGAACCCGTGA | 11252 |
| rs577200883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873521 | TTAGAAGCTAGGCCA[C/T]TGGGCACAGCCCCCA | 11252 |
| rs577221473 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912719 | GCGGCAATTATTTCC[C/T]CTGTTGGAGGGAAGA | 11252 |
| rs577224159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004465 | TTAAAGCATCACCAC[A/G]TGCGAGCTAAGTGGC | 11252 |
| rs577229616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961927 | CCGTCACCAAAAAAG[C/T]AGAGAAGTCAACACA | 11252 |
| rs577237254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874399 | CAGAAAGTCTTCACA[A/G]GCAGAGCACATGTAA | 11252 |
| rs577245061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011096 | TACAAAACTATCCCA[A/C]GAACCACCACTGGGA | 11252 |
| rs577256671 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943119 | TACACTTCTCTTCAT[A/G]AATTTACTCCTATTT | 11252 |
| rs577275093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876630 | TCCTGTCATGGTGCT[C/G]CTAGGGCCTTGAAGG | 11252 |
| rs577295375 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890385 | GCTTTGAGCTCTACC[A/T]CCAATGTATGGTTCT | 11252 |
| rs577320297 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995471 | GACAAGGTTTTTAAA[A/G]CAACTTTTCAGGAAG | 11252 |
| rs577335266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992932 | ACTCTGGGAGGCTGA[G/T]GCGGGCAGATTGCCC | 11252 |
| rs577379035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898497 | GCTGGTCTCAAACTC[C/T]CGAACTCAGGTGATC | 11252 |
| rs577384133 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988737 | TGATCCAATCTAATT[C/G]ATGTTGGCCCCAGCC | 11252 |
| rs577390731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909168 | GCCTTTCCTGCCCTT[C/T]CCCCTGGGCAAACCT | 11252 |
| rs577390773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916257 | TGTCCTTGCTACTTC[C/G]TTCAGCTCCACAGTC | 11252 |
| rs577402586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947319 | AGAGTATTATTGACA[A/G]CATGCATGAGTCAGA | 11252 |
| rs577405360 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919151 | TTTAATAATTAATTG[A/G]GGGCTTCTCATCTGG | 11252 |
| rs577405952 | in-del | -/A | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870906 | AATGAACAGGTGTAT[-/A]AAAAAGTATAACTGT | 11252 |
| rs577406143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940393 | GTCAGCATGTGTTTG[C/T]TGAATGAGTAACACT | 11252 |
| rs577418027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963411 | GGCGGCAAACAACAC[A/G]CAGGGCAGCACTTCC | 11252 |
| rs577454584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909700 | ATAAGAGCTTAATTA[C/G]TGGACTTGTTAAAGC | 11252 |
| rs577478552 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939922 | TAAAGTCCCTGACTT[C/G]TAGAGACTGCATGTT | 11252 |
| rs577492383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982230 | CTCTGCCTGGCCAGC[C/T]GCCCCGTCCGGGAGG | 11252 |
| rs577494404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989568 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 11252 |
| rs577514001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898851 | CAGCTGGAATCTCAA[C/T]CATCCCTGTGCAGAA | 11252 |
| rs577531136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924919 | CTGCCACTACGCCCA[A/G]CTAATTTTTTATATT | 11252 |
| rs577545800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881304 | CCTAACAGCCCCCGA[C/T]AGGAGATGGGTGCTC | 11252 |
| rs577556737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983062 | TGGCTTACAACTGTA[A/C]TTCCAGCACTTTGGG | 11252 |
| rs577562932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894637 | CTTTTTTCGTATATG[A/G]AAAGAAAAACTAGTT | 11252 |
| rs577565533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934734 | TTATTTGGCCCCCAT[C/T]CCTCTTTCCCCAACC | 11252 |
| rs577594599 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954562 | CTGCACCTGGCTAAT[G/T]TTTTATTTTTTATAG | 11252 |
| rs577601499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895216 | AGGAAGTCGGAAGTG[A/G]GCATTTTCACAGCTC | 11252 |
| rs577637107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889510 | GTTTCATTATGAATG[G/T]GGCCAGGGACAAAAC | 11252 |
| rs577658703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001038 | TGGGCCCCGTCCGAC[A/C]TCAAATAAAACTTAG | 11252 |
| rs577676967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918167 | CCAGCTGCACACCAG[A/G]GCCACTGCAGACAGG | 11252 |
| rs577677245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927943 | CATACTCCACTGAGC[C/T]GAGCCCTCATGTCCA | 11252 |
| rs577713177 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889869 | GGGATAAAAACCTAT[-/G]CAAGAGAAAGAAAAA | 11252 |
| rs577721025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919844 | AGCTCAGCCAGGCAC[A/G]GTGGTTCACGCCTGG | 11252 |
| rs577734204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995083 | ATGTCCCCCCTCCCC[A/G]CCTCGGGGCTGCTCC | 11252 |
| rs577736726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906242 | TGACCAAGGGGGACA[A/C]AGGACAGCTTGGTTA | 11252 |
| rs577740654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949453 | GTTAAGCCTCATACA[C/T]ACACGCGCGCGCACG | 11252 |
| rs577779695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906812 | ACGCAATATACACCA[C/T]GTCTACATTTTGTGT | 11252 |
| rs577788230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919001 | TCTGCTTCATTCATT[C/T]TTCCAGGTTGAGCCG | 11252 |
| rs577790112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911594 | CATTTGGCCCTCTGG[C/T]CACTTGCCTGTGTTG | 11252 |
| rs577844448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002673 | TGTTCATACCCTTTA[A/G]TACAAGATTTCTATT | 11252 |
| rs577895279 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933451 | AATTCAAGTCCAAAA[A/C]TAAATGACAAAATAA | 11252 |
| rs577950958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943094 | TTTGTAATTTTCAGA[A/G]TATAAGTCTTACACT | 11252 |
| rs577953533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907709 | GCTCAGGGCACTGCT[C/G]TGCCGCCTCCTAACT | 11252 |
| rs577958269 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944477 | AACATTGCTAATAGG[C/T]TTCATGGAAAAATCT | 11252 |
| rs577968498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014209 | TTCGGATTTCTGATT[C/T]AGTGAGTCTGGGGAA | 11252 |
| rs577986696 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915096 | TGGTCTCAAACTCCT[A/G]GGCTCAAGCGTTCCT | 11252 |
| rs577987834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975187 | CAATGCCAATACTCA[A/G]TTATTAGCATGGAGG | 11252 |
| rs577996186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884266 | GGAGGCCCTGAGGGC[A/G]GTGAGGAGACCTCCT | 11252 |
| rs578003801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882557 | CCCTGCTCTGTGTCA[C/T]ATATGCAAAAGGCAC | 11252 |
| rs578045977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014991 | GCGCCCCAACCGTCG[C/T]GGCGACCCCTGACCT | 11252 |
| rs578050576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926538 | TAGGAACTCCACGAG[C/G]ACACAGAATCACTTC | 11252 |
| rs578093820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932084 | TGTACTGCAAATCCC[A/G]TCATGACCCGGCCCC | 11252 |
| rs578096754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920367 | TTAGAATGGGGTGGT[C/G]TGTGCTGAGTTATTC | 11252 |
| rs578106920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877421 | AGTGACAGTGTGGGA[A/G]GGGCCGGCTCCCATG | 11252 |
| rs578112199 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979896 | CCCTGCTTATGCCAA[A/C]TGTACTTGTCATTGT | 11252 |
| rs578136606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877999 | ATCCACTTCAGCCTG[A/G]CAAGTGGTACTTGAC | 11252 |
| rs578138959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890382 | TGGGCTTTGAGCTCT[A/T]CCACCAATGTATGGT | 11252 |
| rs578160371 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951101 | TCACTTAATTGTTCT[C/G]CCATAAGAATACACT | 11252 |
| rs578173305 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005947 | GAATGGGACTAGTGT[C/T]CTTACAATTTTTTTT | 11252 |
| rs578181668 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996080 | AAAAAATTAGCTGGG[C/T]GTGGTGGTGGGCGCC | 11252 |
| rs578191038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990396 | GAGCTAAGAACTGCA[C/T]ACTACAATACAAAAT | 11252 |
| rs578211683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901003 | CATGCAGCACACAGG[C/T]CCTGCTCCTGTCCCC | 11252 |
| rs578225291 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956938 | AAGATAAGAAGGTCA[A/T]TTATACACTAAGAAA | 11252 |
| rs578231579 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875885 | GCCATTTTGCCCAGG[G/T]TGGTCTCATACTCCT | 11252 |
| rs578262496 | in-del | -/AA | 0.419936 | 0.183362 | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996532 | GCAAGACTCTGCCGC[-/AA]AAAAAAAAAAAAAAA | 11252 |
| rs745313089 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949587 | CGAATTACAATATAC[A/T]ATAATATTATCTGAG | 11252 |
| rs745343151 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960999 | CTAGAAGATACACAT[A/G]CACACTCCCCCATTC | 11252 |
| rs745346041 | snp | C/T | 8.28562e-05 | 0.00643593 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882177 | CATGGGCACACCCTC[C/T]TCTTACCTCAAACTG | 11252 |
| rs745347241 | snp | C/T | 1.65888e-05 | 0.00287996 | synonymous-codon, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871468 | CTTGGTCAGCTCATC[C/T]CCTGCAAGACAAAGA | 11252 |
| rs745350611 | in-del | -/TCAA | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873179 | ATTAGAAGGTTCATT[-/TCAA]TCAGTTTGCTTTTGA | 11252 |
| rs745354899 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912455 | AACTGGTAGGGCTAG[A/G]ACCCGGGATAAAACG | 11252 |
| rs745374682 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885294 | TGGTACACACTTCCC[C/T]GCACCCCCTCATCTC | 11252 |
| rs745374970 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938709 | TGCCTGGCTGGTGAA[A/G]AGCCTTTCTCCCACT | 11252 |
| rs745388500 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875695 | TGCCCCGCCACACGC[C/G]TGGCTCATTTTTGTA | 11252 |
| rs745401916 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939183 | AAAACTCGTTTATCT[C/T]ATGCAATGGGAACAC | 11252 |
| rs745450028 | snp | C/T | 1.70624e-05 | 0.00292077 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876088 | AAGACCGCCCACAGC[C/T]TGCAGGTTGGAAGCC | 11252 |
| rs745496342 | snp | A/G | 1.69703e-05 | 0.00291288 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884601 | CAGAGGTTCATTTCC[A/G]TTTAGCCCTTGGCTC | 11252 |
| rs745516771 | snp | A/C | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959855 | CGTACCTGCCTCTTT[A/C]CAACCCTGCTGGCAT | 11252 |
| rs745523623 | in-del | -/ACAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987449 | CTGAGTCCAGGAGCA[-/ACAC]ACACACACACACACA | 11252 |
| rs745527776 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992674 | TGTAACATCTTTTCA[C/T]GACATAGCATCTTCA | 11252 |
| rs745529550 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003163 | TACTTGATCAAGATA[A/C]ACAAAAACCACTTTG | 11252 |
| rs745556786 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960647 | GTACGATTCCCTTTG[C/G]ATCCAGCACAAGAAA | 11252 |
| rs745571840 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948753 | TCAAGAAAATATTCT[A/G]TTTCATTCAAAGGTA | 11252 |
| rs745607984 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956007 | GTTCCAAATTGGGAA[C/G]TTCAACATTTTGTCC | 11252 |
| rs745608430 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893822 | ATACACATCAGTGAA[C/T]GGGGGCTTCTCAATG | 11252 |
| rs745608807 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888881 | AGACCATGGGAATGC[C/T]TGTGCTACCAAGAGG | 11252 |
| rs745638076 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918175 | ACACCAGGGCCACTG[C/T]AGACAGGCCACACCC | 11252 |
| rs745648529 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919721 | GAGGTTGTAGTGAGC[C/T]GAGATTGCACCACTG | 11252 |
| rs745662027 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894968 | GAAGGGCTGTCCCTG[A/C]GGCTGAGCTACATGG | 11252 |
| rs745668624 | snp | C/T | 1.66048e-05 | 0.00288134 | missense | PACSIN2 | GRCh38.p7 | 22:42891141 | TCTCTGCCTCGGACA[C/T]GAAGGCCATCCAGGC | 11252 |
| rs745670030 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928970 | ATTCAACAAGCTCTT[-/A]AGAGTTCTCTGAGTT | 11252 |
| rs745682300 | snp | C/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892984 | CGGTGGGGACAGAAG[C/G/T]GGGTGAAACCTCTGC | 11252 |
| rs745693098 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951390 | CACACTAGTTTCCTG[A/G]GTGACCCTCTCCCTC | 11252 |
| rs745706633 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999140 | GCCGTCCTCAGACAG[A/G]AGGGCTAAAAGAGCA | 11252 |
| rs745708750 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917152 | GGTTTCGCCATGGGC[A/G]TTGTCAAAGCAAGGA | 11252 |
| rs745714921 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42873996 | GGTTTCACCATGTTG[C/G]CCAGGCTGGTCTCAA | 11252 |
| rs745753150 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007515 | CCCCTCTCTCCCAGC[A/C]ACTCCTTGTTCTTCA | 11252 |
| rs745758475 | snp | A/G/T | 0.000216063 | 0.0103917 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891220 | GGGTCACTCAGCGCC[A/G/T]GCCATGGTGGGGTCT | 11252 |
| rs745758662 | snp | A/C | 1.68258e-05 | 0.00290045 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879198 | GCCGAGGGAGAGAAA[A/C]CAAAGGTTCACTACT | 11252 |
| rs745792814 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978104 | TCATTCATTCATTCA[C/T]CCCACAATGAGCACC | 11252 |
| rs745819117 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998021 | CAGAGCTTTCCTGGA[A/G]AAGAGGTTTCTCAGG | 11252 |
| rs745822264 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920793 | CATGAATTATCACAC[-/T]TTTTTTTTTTTTTTT | 11252 |
| rs745845688 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966929 | TCGGTGTGATTTTTT[C/T]CCCCTCATTTATTTA | 11252 |
| rs745856642 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928553 | TTTAATATGTAAGTT[G/T]TCAGAGTGTTTCACT | 11252 |
| rs745874831 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974340 | TTCACCTGTTAATTA[C/G]ATATGATCTACTTCT | 11252 |
| rs745879138 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962124 | GTGAAACCCCGTCTG[C/T]ACTAAAAAATACAAA | 11252 |
| rs745882948 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999597 | CGCTTGAACCCGGGA[C/T]GCGGAGGTTGCCGTG | 11252 |
| rs745902419 | snp | C/T | 0.00028393 | 0.0119115 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909498 | ATCACTGAGCAGTCA[C/T]TCCGCCACTCAACGA | 11252 |
| rs745910196 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887037 | ACCTTTTTGGGCACC[A/T]GATTCCCTGGGATTC | 11252 |
| rs745919320 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934954 | AGAGTTTCGCTTTAT[C/T]GCCCAGGCTGGAGTG | 11252 |
| rs745960579 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899391 | CTCCCGGGTTTAAGC[A/G]ATTTTCCTGCCTCGG | 11252 |
| rs745976308 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908372 | TCCCAGAGCCTACTG[A/T]ATGAAGGTAAGGGAG | 11252 |
| rs745988240 | snp | C/T | 4.94694e-05 | 0.00497316 | missense | PACSIN2 | GRCh38.p7 | 22:42884459 | AGCGAAGGCGTTTCT[C/T]CTCGAACTGCTGGCA | 11252 |
| rs746004941 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004535 | ACCCACTAATAGCGG[A/G]CTTGGACGTCTGTAC | 11252 |
| rs746005375 | snp | A/G | 1.6566e-05 | 0.00287797 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876258 | CCCATTGGCATCCGT[A/G]GAGGAGAAGGGGTTG | 11252 |
| rs746020320 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910019 | AATACTAGGATATGG[A/G]TACCGTTATTACCCC | 11252 |
| rs746021963 | snp | A/G | 1.67744e-05 | 0.00289602 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876356 | AAAGGGGAGGCCACA[A/G]GGCCCTCAGCACAGG | 11252 |
| rs746081151 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956756 | AACAGCAGCCCCAGG[A/G]GGCTGCCGTTTAACC | 11252 |
| rs746083672 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872555 | ATTTTGTATGGCAGC[A/G]ATGCTGGTCAACATG | 11252 |
| rs746112580 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973439 | ACTGTTTTTTGTCAA[C/G]AAGGCTCCACTGAAG | 11252 |
| rs746123719 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988599 | AAGAAAATAATGTAG[C/T]CACAGGTATGAAGAT | 11252 |
| rs746125251 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882048 | TTGGTCTGTACTATA[C/G]CTATGCCTAAAGGCT | 11252 |
| rs746132867 | snp | C/T | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871766 | TCCATAGGGCTGTGC[C/T]TTCCTCACCACCCTG | 11252 |
| rs746134703 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946623 | CCCAGTTACACAACA[C/T]ACAAAGCTGCCTGCC | 11252 |
| rs746172279 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941108 | TCTATGGATTTGCCT[A/G]TGCTGGACATTTCAG | 11252 |
| rs746191496 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953905 | AGGAAAGCCAGGGAA[A/G]AGAGGAATGCTTAGA | 11252 |
| rs746204949 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904458 | ATGCAGGCATCACCT[C/T]GCTGGAAGAGCTGCC | 11252 |
| rs746236781 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930315 | CTGTGCTCTCTGCCC[C/T]AATTCCACAGCCACA | 11252 |
| rs746270754 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009747 | TGGCCACAGAATATG[C/T]ACTATAAACCACCAC | 11252 |
| rs746307818 | snp | C/T | 3.32248e-05 | 0.0040757 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879098 | CTGGTTGATGCCCGT[C/T]AGGGTGACGCCGTCA | 11252 |
| rs746324218 | snp | C/T | 2.92676e-05 | 0.0038253 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871330 | GGCCCGCCGCCTCCG[C/T]CCCCCCGCTGGCCTG | 11252 |
| rs746331036 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994419 | GCCGTGTCCTGCGCC[A/G]CAAAGACCCTCGGGC | 11252 |
| rs746332629 | snp | C/T | 1.67548e-05 | 0.00289432 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893608 | AGTCCGCTTGTAGTT[C/T]CCGACCTAGGAGAGA | 11252 |
| rs746360540 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963370 | AAGACCAGCAGCGCC[A/G]CCCATCAGCTCAGGC | 11252 |
| rs746369584 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878454 | CAGGTCCTATAGGAA[C/G]ACCTCCTCTAGCACA | 11252 |
| rs746384078 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995302 | AGGAAGCAGAGCTAC[A/G]AAGTTATTCAATGCA | 11252 |
| rs746387463 | in-del | -/ATTTTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009865 | CATTTTATTTTTTCT[-/ATTTTTTT]TTTTTTTTTTTTTTG | 11252 |
| rs746460503 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939932 | GACTTCTAGAGACTG[A/C]ATGTTAGTGGCAATC | 11252 |
| rs746511174 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929427 | TTCTCATTGAAGATG[C/T]TGTCAATAGCTTCTG | 11252 |
| rs746521276 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913297 | CCAGCCTGACCAAGA[C/T]GGAGAAACCCCGTCT | 11252 |
| rs746531257 | snp | C/T | 0.000149052 | 0.00863157 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888664 | AACATCTTGCTTGCA[C/T]TTTTCTATTTTGTCT | 11252 |
| rs746536583 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940567 | CAGAATATGAGCCCC[A/G]CCCTGGGACAGGGCA | 11252 |
| rs746541383 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902805 | TTTTAGTAGAGACAG[G/T]GCTTCGCCATGTTGG | 11252 |
| rs746549925 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008545 | TTAGCCACCACGCCC[A/G]GCCTAAGTTCAGTGT | 11252 |
| rs746551535 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959063 | AGTGTCTAGTGACAG[C/T]CCTCAGAGGGGGACG | 11252 |
| rs746595579 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900544 | TGGAGTGCAGTGGCA[A/C]AATCACAGAGGCGCA | 11252 |
| rs746602470 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912470 | GACCCGGGATAAAAC[A/G]TGAGTGGAGGTAATC | 11252 |
| rs746620909 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943276 | CTGTATATTAATTCT[-/A]AGAGTTTTTTTGGTG | 11252 |
| rs746623331 | snp | C/T | 1.65622e-05 | 0.00287764 | missense | PACSIN2 | GRCh38.p7 | 22:42888789 | GGTGGGCTTTCTTTG[C/T]TGCTTCTACCTACAG | 11252 |
| rs746632811 | snp | C/T | 1.65636e-05 | 0.00287776 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876995 | CTGGGCGGGGTTGCT[C/T]GGGACATTAAGGGTG | 11252 |
| rs746659926 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949985 | AAGTGAATAACACCA[C/T]GCAGGCCCTGCGGTC | 11252 |
| rs746685632 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978394 | TCCAATAACCTATAA[C/T]GCTGAGAAATCTAAC | 11252 |
| rs746717218 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949683 | ACACACACATACACT[-/CA]CACACACACACTCAC | 11252 |
| rs746738930 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983407 | AGGCAGGAGGATCAC[C/T]TGAACCCAGAAGGCG | 11252 |
| rs746746999 | in-del | -/CTGCACCCCAGC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997842 | GCTGAGATCACACCA[-/CTGCACCCCAGC]CTGGGCGACAGGGCA | 11252 |
| rs746775544 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908698 | TTCCCATTTTGCTCC[A/G]AAACTGGCCCTTAGC | 11252 |
| rs746804059 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970962 | TGCCCCCAGCCTCTC[C/T]ACAGCCCTCTCTGCT | 11252 |
| rs746818664 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914699 | ATCAAGCCACCAGCT[C/G]GGCTGCCTGGCCAGC | 11252 |
| rs746822729 | snp | A/C/T | 1.65847e-05 | 0.0028796 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882152 | AGGTCCTCTTCCAGG[A/C/T]TGATGAGCTCATGGG | 11252 |
| rs746828370 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919126 | ATGCAAAAAATATGT[A/G]AAATGTGTATTTAAT | 11252 |
| rs746832181 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916784 | ATAAGGTGATTTCCT[C/T]GCAGGCATGGAGAAG | 11252 |
| rs746851100 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015402 | CTCCCAAAGCCGCTC[C/G]CTGGTGGTGGTCCTT | 11252 |
| rs746857313 | snp | A/G | 1.65688e-05 | 0.00287821 | missense | PACSIN2 | GRCh38.p7 | 22:42882215 | TTCATGGCCATGCCC[A/G]GCCCGTGATTGGCTC | 11252 |
| rs746872054 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891650 | ACCTCAGGTGATCCA[A/T]TCGCCTCGGCCTCCC | 11252 |
| rs746874633 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989402 | ACTAAGGAGGCTGAG[A/G]CAGGAGAATCGCTTG | 11252 |
| rs746875375 | snp | G/T | 1.69338e-05 | 0.00290974 | missense | PACSIN2 | GRCh38.p7 | 22:42882299 | TCATGGTAAATGGCT[G/T]TGTAGCTAAATCAGA | 11252 |
| rs746879938 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918252 | AGCTGCCTCATGGCA[C/T]CATGCAGTGTTCAAA | 11252 |
| rs746894879 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936950 | AGTAAATTAAATTAG[C/T]AAATACCTATTTACA | 11252 |
| rs746907377 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999220 | CCTCGGCCCCTGTAC[C/T]TGCTCACCTGCATGC | 11252 |
| rs746915057 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009380 | ATACAAGTCATCATT[A/C]TTATTAGCTCAAAGA | 11252 |
| rs746931022 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968046 | GGGAGTACTGCGCCA[C/G]TTTTCAGATGAGAAA | 11252 |
| rs746963305 | snp | A/G | 1.65721e-05 | 0.0028785 | missense | PACSIN2 | GRCh38.p7 | 22:42876191 | AGTCATACAGGGCCC[A/G]GACTCGCACTTCCGT | 11252 |
| rs746963771 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000003 | CCATCTGCACAACAA[A/T]CCTATCATGATCCCC | 11252 |
| rs746979980 | in-del | -/AT | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42995224 | CCCTGGCATTCAGTC[-/AT]GTTTCACAATAACTC | 11252 |
| rs747038769 | snp | G/T | 1.65726e-05 | 0.00287855 | missense | PACSIN2 | GRCh38.p7 | 22:42884543 | GTTCCTTCAGGGACT[G/T]CTCATACTTCTCTTT | 11252 |
| rs747056133 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926410 | TCTCCAGGCAGACAC[A/T]ACTCATTGTTGCTAT | 11252 |
| rs747087128 | snp | C/G | 3.37285e-05 | 0.00410647 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876366 | CCACAGGGCCCTCAG[C/G]ACAGGGCGGCAGAGG | 11252 |
| rs747110943 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927504 | TCCACCCATCTTGGC[C/T]TCCCAAAGTGCTGGG | 11252 |
| rs747125771 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901154 | CCCAAGCACCACAAC[C/T]GCTCCCTCTGCACCC | 11252 |
| rs747128410 | snp | C/T | 1.65622e-05 | 0.00287764 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876881 | GAGGAAGCATTTGTT[C/T]ACCAACTTTTTGGCC | 11252 |
| rs747169078 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995501 | GTTACTCTGTCCATT[A/G]GGCAGGACCTTAAAA | 11252 |
| rs747179560 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974503 | CAGAAGTACCACATA[C/G]AGGCTTCTTGTCTGG | 11252 |
| rs747215540 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010138 | TTCCCATAGTGCTGG[A/G]ATTACAGGTGTGAGC | 11252 |
| rs747230655 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963415 | GCAAACAACACGCAG[A/G]GCAGCACTTCCCAGG | 11252 |
| rs747238738 | snp | A/G | | | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873491 | GGGTGCTGAGGGGAG[A/G]AGGCTGAAGACTGGT | 11252 |
| rs747258938 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005207 | CATTTGCTTTCTAAG[G/T]CCTATTTCCCATCAC | 11252 |
| rs747311456 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970305 | GGCACTTCACCTCTG[C/T]GGGACTCTCCCCAAA | 11252 |
| rs747337520 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943842 | TGAATGTGTCCAAAA[C/T]TTACGTTAAACTTTT | 11252 |
| rs747372301 | snp | A/G | 5.03419e-05 | 0.00501681 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893611 | CCGCTTGTAGTTCCC[A/G]ACCTAGGAGAGAGAA | 11252 |
| rs747384969 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979962 | ATACATACAATACAC[-/AT]ATAGTATAAATACAC | 11252 |
| rs747390848 | snp | C/T | 0.000843407 | 0.0205181 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909537 | CATGGAGAAGGCGGA[C/T]GACCACAGCACTGCG | 11252 |
| rs747417566 | snp | G/T | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871421 | TTGTCCAAGCGTCCC[G/T]TGCACCAGCCCTGCT | 11252 |
| rs747441268 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996697 | GCCCTGTCTCAATCA[A/G]GGGGAAAAAAAGCAG | 11252 |
| rs747442636 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012192 | ACATACATACATACA[A/T]ACATACATACAAACA | 11252 |
| rs747451792 | in-del | -/TGT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886455 | GTAGGTAGGTAGGTA[-/TGT]ATGTACCTACCTACT | 11252 |
| rs747479790 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984129 | GTGTGCACCACCACA[C/T]CTGGCTAATTTTTAT | 11252 |
| rs747510448 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869574 | ACAGCAGCAGGTCTC[A/G]GGGAGAAGGGAACCC | 11252 |
| rs747511311 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954177 | CTGAGGCAAGAGAAT[C/T]ACTTGAACCTGGGAG | 11252 |
| rs747526522 | in-del | -/ACCCAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987492 | CACACACACACACAC[-/ACCCAT]GGCACCATGTTCAGA | 11252 |
| rs747566534 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955147 | CACCCTGCTGCTTAG[A/T]AGTCTCTTTACCTTA | 11252 |
| rs747574191 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895369 | GGAGCTGAGGTAACA[A/C]GGCCCTAACTTAGCC | 11252 |
| rs747593287 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968966 | TCTCCAGCTTGCAGG[A/C]AGCCTGTCATAGAAT | 11252 |
| rs747596530 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919304 | ATGGGCTCTCATTAC[C/T]TCCCAGGGTATTAAG | 11252 |
| rs747604508 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004855 | TATGGGGTCCTGGCA[A/G]GTGGCCTCAGGCAAA | 11252 |
| rs747620597 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930185 | ACAGTGTGGTGTGCC[C/T]ACCAGCCATGCCACC | 11252 |
| rs747636907 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977913 | TTAAACCTCTTTTCT[C/T]CATAAATCACCCAGT | 11252 |
| rs747648820 | in-del | -/AA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989861 | TCTCTTGGAGGGGGA[-/AA]AAAAAATATATATAT | 11252 |
| rs747679188 | in-del | -/TCTA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942750 | TTTTGTTTTCTTGAC[-/TCTA]TCTCATTTTTCCATG | 11252 |
| rs747743136 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922412 | CAAGAACATTCTGAG[-/T]TAAAAAGACCATGTT | 11252 |
| rs747754393 | snp | C/T | 3.34801e-05 | 0.00409132 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42890956 | ATGTACCTCTTTCAG[C/T]TTCTTGGCCCAGGGC | 11252 |
| rs747767644 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009627 | ACCTCAGGGTTGGTC[A/C]GGGAAAGGCTGGACA | 11252 |
| rs747780862 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920166 | GAAAAAAAGAAACTG[A/C]GCTCCAATACCGGAA | 11252 |
| rs747782188 | snp | C/T | 1.67612e-05 | 0.00289488 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871333 | CCGCCGCCTCCGTCC[C/T]CCCGCTGGCCTGTCC | 11252 |
| rs747798003 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940142 | CACAGATGTTACCTA[A/G]TACTATTCCTACACA | 11252 |
| rs747816009 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979361 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 11252 |
| rs747834064 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952593 | CAGTCTCCTGACCTC[A/G]TGATCCGCCCACCTT | 11252 |
| rs747834841 | in-del | -/AA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979785 | GAGGACAAAATCCCT[-/AA]GTTATTAATGGATTA | 11252 |
| rs747849424 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948306 | AGAGTGACTTCTGCT[C/T]CATTTACCTACCAGC | 11252 |
| rs747899814 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903581 | TCATCCACCACTGGG[C/T]TCCCAACTTGTCTCA | 11252 |
| rs747919255 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936772 | AAAAATTAGCCAGGT[A/G]TGGCAGCACACATCT | 11252 |
| rs747953461 | snp | A/G | 1.72341e-05 | 0.00293543 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882316 | GTAGCTAAATCAGAG[A/G]GAAACGTGGCTCTTT | 11252 |
| rs747961557 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016415 | GTACTCTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 11252 |
| rs747981089 | snp | A/C/G | 4.96951e-05 | 0.00498452 | missense | PACSIN2 | GRCh38.p7 | 22:42876238 | TCGTCGAATGGATTC[A/C/G]AGTCCCCATTGGCAT | 11252 |
| rs747988027 | in-del | -/AGAA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003724 | AGTGCAGTCCTCTAC[-/AGAA]AGAAACACAATTTCT | 11252 |
| rs747996026 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909977 | GCCCTAAAACACTTA[A/G]CGTTTATTCATTCTT | 11252 |
| rs748014588 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985616 | AAACATTTGCAAAAC[-/AT]ATAAAGATAACAGGA | 11252 |
| rs748039468 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877922 | CCCCAGAACCAAGGA[A/T]GGGAGGCGAGGACAT | 11252 |
| rs748047241 | snp | C/T | 1.6569e-05 | 0.00287824 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876204 | CCGGACTCGCACTTC[C/T]GTCCCCGAGGTGGCG | 11252 |
| rs748068482 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42873938 | GGATTACAGGTGTGT[A/G]CCACCATGCCTGAAT | 11252 |
| rs748085486 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958638 | GGCCCGATTAAGGTC[A/G]GACAGACATACTATA | 11252 |
| rs748137643 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883389 | CAGAGGGAGACAAAC[A/G]GAATGTGTCTCCTAT | 11252 |
| rs748138682 | snp | C/T | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959636 | TTAATAATGAACTAA[C/T]TGAACATTGCCGTCA | 11252 |
| rs748225364 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950948 | CATTAAGGGCTGGGG[A/G]AAAGCATGAAGCCAA | 11252 |
| rs748233327 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905530 | CCCATCACAGAACAG[C/G]AGCAGGCCATCACTG | 11252 |
| rs748240760 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891557 | AGGTGCCCGCCACCA[C/T]GCCTGGCTAAATTTT | 11252 |
| rs748241783 | snp | A/G | 1.72913e-05 | 0.0029403 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893414 | GCCCCCGGCTGGGGT[A/G]TAGCTGCCTCCAGGC | 11252 |
| rs748256230 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915699 | AGTAAAACAGAATTA[A/G]GAAGACAAATCTTTT | 11252 |
| rs748275461 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894766 | CTGGCTTGAAAGGCT[-/AC]AGTCGCTGATAACTT | 11252 |
| rs748281146 | snp | A/G | 1.65729e-05 | 0.00287857 | missense | PACSIN2 | GRCh38.p7 | 22:42882222 | CCATGCCCGGCCCGT[A/G]ATTGGCTCGGAACCA | 11252 |
| rs748339646 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915551 | AGCTCAATCTGTAAT[-/A]ACATCAGCTCAACTA | 11252 |
| rs748358959 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954239 | CTGCACTCCAGCCTA[C/G]GCGACTGGGCAAGAC | 11252 |
| rs748429954 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927568 | TCTTTTATTTATTTA[G/T]TTATTTAGTTATTTA | 11252 |
| rs748432370 | snp | C/T | 6.63262e-05 | 0.00575836 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912069 | AACGGAATCATCATA[C/T]GTGACAGACATTTTT | 11252 |
| rs748435053 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973815 | TTGGCACCTAGCACA[C/G]GGCTTAGGGTCTAGG | 11252 |
| rs748435067 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890578 | CAAAAATTAGCAGGG[C/T]GTGGTGGCATGTGCC | 11252 |
| rs748437205 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901705 | CCTAACTTCTTGCTA[A/G]GCCATTTCTTCACCC | 11252 |
| rs748452556 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960675 | AAAAGGCGTAACTAA[C/T]CTACACCCTTCGAAG | 11252 |
| rs748454787 | in-del | -/GTTT | 1.69052e-05 | 0.00290728 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884376 | TGTTTTAGCTCAAAG[-/GTTT]GAAACTTACCCAGCC | 11252 |
| rs748455656 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982897 | AAAAAAAAACAACAA[A/C]AAGGCTAGGAGCAGT | 11252 |
| rs748468543 | in-del | -/AAATAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989866 | TGGAGGGGGAAAAAA[-/AAATAT]ATATATATATATATA | 11252 |
| rs748523111 | in-del | -/TAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886453 | AGGTAGGTAGGTAGG[-/TAT]GTATGTACCTACCTA | 11252 |
| rs748581754 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985731 | CTCTTCACCACATTA[C/T]ATTCAGAGGGAGGGC | 11252 |
| rs748582335 | snp | C/G | 6.66744e-05 | 0.00577345 | splice-acceptor-variant | PACSIN2 | GRCh38.p7 | 22:42884562 | ATACTTCTCTTTGGT[C/G]TAAAGGAAAATCCAG | 11252 |
| rs748585853 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871269 | TGGAACCATCATCTC[C/T]TGCAGGAAAAGGAGT | 11252 |
| rs748602786 | snp | A/G | 3.31483e-05 | 0.004071 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888630 | GACGTGTAAAAACAA[A/G]TGTACAGTTTACCTT | 11252 |
| rs748602959 | snp | C/T | 3.31175e-05 | 0.00406911 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876904 | TTTTGGCCTTAGTGT[C/T]GTCCTTCTCACTGAC | 11252 |
| rs748667118 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013172 | GTCCCAAAGCAGCAC[C/G]AGCTAAGGATACCAT | 11252 |
| rs748692164 | snp | A/G | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959728 | AGTGAGAAAGAAAAC[A/G]ATTCCGTGAAAATTC | 11252 |
| rs748715344 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945261 | GCAAGAGGAGTCTTT[A/G]GGGAGGGAGCTGACA | 11252 |
| rs748717044 | in-del | -/TTTG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875373 | TGCCCAGGTTATTTA[-/TTTG]TTTGTTTGTTTGCGA | 11252 |
| rs748743460 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941714 | ACGTCGGTTTAGATC[C/T]TTTGCTCATTTTTTA | 11252 |
| rs748753526 | snp | C/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896911 | ATGACTATTTGCCAT[C/T]TGTATGCCTTCTTGA | 11252 |
| rs748765296 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932700 | TTAACTACAAATGTT[G/T]ATTGAGCTGAGAGCA | 11252 |
| rs748796039 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883802 | CAAGGTCAAGAGATC[A/G]AGACCATCCTGGACA | 11252 |
| rs748804683 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990712 | GGTCAGACCACAAGT[A/C]TGGATTTTATTGTGA | 11252 |
| rs748813771 | snp | A/C | 4.97179e-05 | 0.00498562 | missense | PACSIN2 | GRCh38.p7 | 22:42891123 | GGTGCAGCTCGCTCA[A/C]CCTCTCTGCCTCGGA | 11252 |
| rs748818218 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921842 | CTCCCGGGTTCAGGC[A/G]ATTCTCCTGCCTCAG | 11252 |
| rs748838275 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883453 | CACGGTTCTGCTAGA[C/T]GGATGACAGTAATCC | 11252 |
| rs748862469 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002015 | AGGAAAGTCAGTCCA[C/T]GGGGAGGGGACATGG | 11252 |
| rs748881853 | snp | C/T | 9.94431e-05 | 0.00705065 | missense, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871443 | AGCCCTGCTCATCCT[C/T]GTCCTCCATCTTGGT | 11252 |
| rs748913590 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011221 | ATGCAAACTGCCTTC[A/G]TAACTAAGGCATTGC | 11252 |
| rs748922179 | snp | C/G | 0.00014038 | 0.00837678 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909562 | ACTGCGGAGTTGATA[C/G]CAGCTGGAGAGTAAT | 11252 |
| rs748934534 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884679 | GAAAAAACAGGAGCT[C/T]TGGATTCTGACAGAC | 11252 |
| rs748946778 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969341 | CCAACTAATCTGTAA[C/T]CTCATTTCAATTGGA | 11252 |
| rs748950030 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001178 | GGGCAGCTGAGCAGG[A/G]ATTTCTCAGGGAAAT | 11252 |
| rs748964782 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012095 | GGTTACAGTGAGCTG[A/C]GATCGCACCACTGCC | 11252 |
| rs748966043 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977832 | CTTGCTTCCCCTTCC[A/G]CCATGATTGTAGTTT | 11252 |
| rs748996355 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931780 | TTGTTATTATTATGG[C/T]TAACAACCAGGGTAT | 11252 |
| rs749003689 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958857 | TATAATTCACTGAGT[A/G]ATGGGTCACTTAAGT | 11252 |
| rs749011873 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869409 | TGGAGACGCAGATAA[A/T]GTAAGTAAAAAGTGG | 11252 |
| rs749014613 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965693 | TGGTAGAGGATCCAA[A/C]TGGTCCACTTTCTAA | 11252 |
| rs749030715 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895648 | GAAATGTGGAAATCC[A/G]TGATGAATACAGGAA | 11252 |
| rs749056312 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891855 | GGGCACCCACCCACA[A/C]CATGCCAACGCTTCT | 11252 |
| rs749071351 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927611 | GTTATTTTTGAGACT[A/G]AGTTTTGCTCTTCTT | 11252 |
| rs749080372 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953512 | CGTAACAGCATTATT[A/T]GCATTAACAAACCAT | 11252 |
| rs749103846 | snp | C/T | 1.66438e-05 | 0.00288472 | missense | PACSIN2 | GRCh38.p7 | 22:42876332 | TCTCGTAGCTGCTCA[C/T]ACTGCAAGAAAGGGG | 11252 |
| rs749115048 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932309 | TTGGGGCATCCCTTA[C/G]AGAATCTAGCCACAC | 11252 |
| rs749125167 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939950 | GTTAGTGGCAATCGG[C/T]GTCTACCCGGCCTTC | 11252 |
| rs749147118 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976317 | TTCCTATAGAGCAAG[C/G]CCAGAAGCTACACCC | 11252 |
| rs749171272 | in-del | -/AACT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932954 | TGAATCAGAGGAACC[-/AACT]GTGTTAGGAGACGAA | 11252 |
| rs749181361 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897853 | AATTCCAGGCACAGG[A/G]AACAGCACTGGCAAA | 11252 |
| rs749214866 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992331 | GATGCGCGCAAAGCA[A/C]TTTGGAAAAGTTTGG | 11252 |
| rs749235443 | snp | A/G | 1.68562e-05 | 0.00290307 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876365 | GCCACAGGGCCCTCA[A/G]CACAGGGCGGCAGAG | 11252 |
| rs749270204 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977123 | TTCATATGAGACTGA[C/T]CTGTAATTTCATTTA | 11252 |
| rs749288079 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937616 | CTGTGCAAGCAGTCA[C/G]GCATGTGAGTCAGCA | 11252 |
| rs749290182 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949252 | AAATGACACATTGTA[C/T]GTGAGTGCCTGAAAA | 11252 |
| rs749329599 | snp | C/G | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871669 | CCTCTGACAGACCTA[C/G]AGATGACAGTCTCAC | 11252 |
| rs749335936 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946524 | CACTGCACTCCAGCC[C/T]GGGGGAAAGAGCAAA | 11252 |
| rs749336502 | snp | G/T | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42947004 | ATACTTCCCGACGAC[G/T]CCTCCTCTCCGTCAG | 11252 |
| rs749336687 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907584 | AGGCAGGCCATCACA[C/T]GGAAAAGTCCGTTGG | 11252 |
| rs749338433 | snp | C/T | 1.6674e-05 | 0.00288734 | missense | PACSIN2 | GRCh38.p7 | 22:42893523 | CATACGCCTTCTCGA[C/T]GCGCGCCCGCTCATG | 11252 |
| rs749338463 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898603 | GGTCCTCCGGAGGCC[A/G]CTCTCCTGCCTCCCA | 11252 |
| rs749363362 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970481 | AATTTCAAAAAATAA[A/G]CTATGGTTACATAAA | 11252 |
| rs749368669 | in-del | -/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911826 | CTGCCTTCGATGATG[-/TT]GCTAAGGCATACCTG | 11252 |
| rs749370156 | snp | C/T | | | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891121 | GAGGTGCAGCTCGCT[C/T]ACCCTCTCTGCCTCG | 11252 |
| rs749391220 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906874 | CAAAAGAGAAAAAAA[A/G]TACCACACACAATTT | 11252 |
| rs749391775 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933909 | AATATTATGGCGCCA[C/T]GGTAACAGAAACTAT | 11252 |
| rs749401393 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948930 | AACAGGGAACTCAAT[C/T]GTCAGGCAACAATCT | 11252 |
| rs749408293 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918074 | AACTGAGAAGGATGT[A/G]AAAATGCTTTGTAAA | 11252 |
| rs749432041 | snp | C/G | 3.56132e-05 | 0.00421963 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882341 | CTCTTTTAGAAGGCA[C/G]GGGCCAGCTACCCTT | 11252 |
| rs749432192 | snp | C/T | 3.33356e-05 | 0.00408248 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893597 | ATCCGCTTCACAGTC[C/T]GCTTGTAGTTCCCGA | 11252 |
| rs749444046 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986943 | TAAGATCCCCTTCTT[G/T]AGTAAAGTTTATTGG | 11252 |
| rs749495670 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966672 | AATTTTTTTCTTATG[C/T]ATTTTATAGAATCCC | 11252 |
| rs749501402 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955389 | CAGGCAGTGATCTAA[C/T]GGATGGCTGGAAATA | 11252 |
| rs749512992 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944071 | ACTGTGTTGGTAGTC[C/T]TGGCCACATCAGTAG | 11252 |
| rs749559867 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951480 | CCAGATCCGGCATGG[C/T]CCGAGCTGCTGGCTC | 11252 |
| rs749563078 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905131 | AAAAATTTTATCTTC[-/A]GAAGACAAGCTTCTT | 11252 |
| rs749563876 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877661 | CCCAGTGTGGGAACC[A/G]GAGAGATCTGGGCCA | 11252 |
| rs749572490 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892837 | CCTTGAGAAACCCAC[A/T]CTGCTCTGCTTCTGT | 11252 |
| rs749612747 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905176 | CCGAAGTGCTAAATT[-/C]CCTCAACGCAAAAAC | 11252 |
| rs749619045 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887616 | CTCGGCAATCACACC[A/C]CCCAGCCCTCACCCC | 11252 |
| rs749640960 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924497 | GCAAGGCAGACCACA[C/T]TGCTGCTCTTAAGCC | 11252 |
| rs749647460 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913348 | GCCAAGCGTGGTGGC[A/G]TGTGCCTATAATCCC | 11252 |
| rs749651494 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987943 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACAT | 11252 |
| rs749666420 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882404 | CGTGGTCTCTGCCCT[C/T]TGTGAGTTGGTTTCA | 11252 |
| rs749702210 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961312 | TTTAGACAAACACTG[C/T]GGAAGGCCGCAGGGT | 11252 |
| rs749711138 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873032 | TACCATGTGGCAAAC[A/G]GCCAGAACACCGCAA | 11252 |
| rs749730200 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994269 | CTGCTCTTAACCCCA[A/C]CTCCCCATGCAACTG | 11252 |
| rs749736086 | snp | C/G | 1.73399e-05 | 0.00294443 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879006 | TGCCCAGGGCCCCCA[C/G]CATGGAACGGCCTCT | 11252 |
| rs749738703 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926874 | GCTTGGAGGAGGTTA[A/G]GGAAAAACAAACAAC | 11252 |
| rs749739163 | snp | C/G | 1.65614e-05 | 0.00287757 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876983 | TGACTGCGCAGACTG[C/G]GCGGGGTTGCTCGGG | 11252 |
| rs749761836 | in-del | -/AAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989860 | TTCTCTTGGAGGGGG[-/AAA]AAAAAATATATATAT | 11252 |
| rs749776495 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993414 | AACTTATCGCCTGTT[C/T]ATTATAACTCAATAA | 11252 |
| rs749790345 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973350 | TTATTTCCACTTGCT[C/G]AGGAATTGACGAGCA | 11252 |
| rs749790828 | snp | A/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872441 | TTTTGCCTTTATTGC[A/T]AAGTTTGAAGTTTTG | 11252 |
| rs749812503 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004405 | ACATGCCCAGTCTCC[C/T]TATCTGATGACACAT | 11252 |
| rs749820462 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934921 | TTCTTCCTTTTTCTT[C/T]TTCTTTTTTTTTGAG | 11252 |
| rs749842246 | in-del | -/ACC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959492 | CACGTATGTTCTAAA[-/ACC]ACCAGAGTCAAAAAT | 11252 |
| rs749855119 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899341 | GCCCAAGCTGAAGCG[C/T]AGTGGTGCCATCTCG | 11252 |
| rs749869981 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923007 | GAGGGGTCTTTCCGG[A/C]AGAGGCAGAGGGAGT | 11252 |
| rs749873683 | in-del | -/TGAGACTGCATCTA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966350 | GGCCTGGCGACAGAG[-/TGAGACTGCATCTA]AAAAAAAAAAAAAGC | 11252 |
| rs749883576 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961266 | TAACACAAAACGAAG[C/T]AGGTTAAAAATCTCT | 11252 |
| rs749900561 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899615 | AGACTGGGCAGGCCT[C/T]TGTGCACAACTAGGC | 11252 |
| rs749902668 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886328 | ACTAAATGCAAAAAG[C/T]TCTTTTATGATGGAT | 11252 |
| rs749907108 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953299 | TCTAAACTAAGAGTG[-/A]AAAAAAAAATGCAAT | 11252 |
| rs749937031 | in-del | -/G | 3.31494e-05 | 0.00407107 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876863 | GTGAGCGCGGTGGGA[-/G]CAGAGGAAGCATTTG | 11252 |
| rs749982048 | snp | G/T | 1.6588e-05 | 0.00287988 | missense | PACSIN2 | GRCh38.p7 | 22:42876172 | TCATGCTCCTGCCCC[G/T]CATAGTCATACAGGG | 11252 |
| rs749996141 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013044 | TGATCTGCCCGCCTC[A/G]GCCTTCCCAAGTGCT | 11252 |
| rs750017040 | snp | A/G | 1.67654e-05 | 0.00289524 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42882286 | GCTCTGCTCCAGGTC[A/G]TGGTAAATGGCTTTG | 11252 |
| rs750017624 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004259 | GAGAACACTATCTGG[C/T]TGCAAGAATTAAATG | 11252 |
| rs750019106 | snp | A/G | 1.66266e-05 | 0.00288323 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893557 | GCAGTTCATGAGGTC[A/G]CTGCACAGGCGGTGG | 11252 |
| rs750024934 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874964 | CAAGCAATTTTCCTG[C/T]GTCAGCCTCCCGAGT | 11252 |
| rs750037671 | snp | G/T | 3.42495e-05 | 0.00413807 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884363 | TTCAATGACGTGTGT[G/T]TTTTAGCTCAAAGGA | 11252 |
| rs750069529 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881734 | ACTGCCTGGAGTAGG[C/G]AAAAGTCCTTTGTTG | 11252 |
| rs750077905 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989869 | AGGGGGAAAAAAAAA[-/T]ATATATATATATATA | 11252 |
| rs750117821 | snp | A/G | 3.31318e-05 | 0.00406999 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876222 | CCCCGAGGTGGCGTC[A/G]TCGTCGAATGGATTC | 11252 |
| rs750119016 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973147 | CAGTGAAATATTCCT[A/G]TCCAAAATGCCCTGC | 11252 |
| rs750160141 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010852 | ATAAGCACAATTCAA[C/T]AGGTAACTTAAGGAA | 11252 |
| rs750160250 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946099 | CTGAACAAATGCACA[A/G]ATGAATTAGAGGAGG | 11252 |
| rs750169205 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878940 | CACAGAGCTCAGGAG[C/T]CCAGGAACCTCCCAG | 11252 |
| rs750175953 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904079 | CAGAAACCCAGAAAT[C/T]GCAATTTTCAGATCC | 11252 |
| rs750188926 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980048 | AACTATTAAAACAAG[G/T]TTCTATTAAAACAAG | 11252 |
| rs750201571 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953260 | TCTAGGATAACCACT[A/G]AAGGAGCAGGCTGAG | 11252 |
| rs750229344 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913997 | ACAAAGTCCACAACA[G/T]ATAACGGTACTTCAA | 11252 |
| rs750229409 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903258 | CCACCTTCCCTGGGG[A/T]GGGTGTGCGTGTGCC | 11252 |
| rs750252863 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941809 | AGTCTCACTCTGTCA[C/T]TCTGTCACCCAGGCT | 11252 |
| rs750255821 | snp | A/G/T | 3.31177e-05 | 0.00406914 | missense, synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876953 | CTCATCCTCGAAGGG[A/G/T]TTGTAGCTGGACTGT | 11252 |
| rs750286606 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009298 | ATTGCCACCTGTACC[A/G]CTCAGAAATGTTTTG | 11252 |
| rs750288027 | in-del | -/TACATAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012160 | AAATAAATAAATACA[-/TACATAC]ATACATACATACATA | 11252 |
| rs750294350 | in-del | -/TTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983967 | CAGCACTTAGCACTT[-/TTTT]TTTTTTTTTTTTTTT | 11252 |
| rs750316841 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878166 | AGCCCAGGGCCCCCA[A/G]GGTCTCCTCTGAGGC | 11252 |
| rs750400603 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990195 | CTGCAGTCAGTCAAC[A/G]TGACTTTCCACATGA | 11252 |
| rs750417888 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994837 | ATATCCACACCTAGA[G/T]CCACAGCCTCGCAGC | 11252 |
| rs750423573 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913180 | CTCGCTTGCCTTATC[C/T]GGAAAAAAGAGACAA | 11252 |
| rs750433204 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909538 | ATGGAGAAGGCGGAC[G/T]ACCACAGCACTGCGG | 11252 |
| rs750437555 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001627 | GTATGCCTGTGCTGT[C/T]TGTGGCTGTTTCCTC | 11252 |
| rs750458247 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947521 | AACAGTCTGATGAGT[A/G]GAATCCTCAAGAGGA | 11252 |
| rs750486546 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009277 | CATCACAGGAAGGAA[-/T]TATCTATTGCCACCT | 11252 |
| rs750514898 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948096 | CTTCAGCAGGAGCAG[C/G]AAGGAAAGGCATCCC | 11252 |
| rs750517924 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936344 | TCTGGCAAACAATCC[A/G]TGTTGGTTCCCTTCC | 11252 |
| rs750543173 | snp | C/T | 0.000435628 | 0.0147521 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912132 | GTCAGGGGTCAACTT[C/T]GAACGCTCAAAATCT | 11252 |
| rs750591319 | snp | A/G | 1.65154e-05 | 0.00287358 | missense | PACSIN2 | GRCh38.p7 | 22:42884528 | GTGTGCCCTGGTCGA[A/G]TTCCTTCAGGGACTT | 11252 |
| rs750598864 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903495 | CCTTGCTTTCAGGTG[C/T]CAAACTGCAATTTCC | 11252 |
| rs750613860 | in-del | -/AA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955794 | TGGGAAAGTAGTAAC[-/AA]AAATGTTTCTGTCTT | 11252 |
| rs750632783 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000832 | TAAAAGGAGACATAC[C/T]GTGTGGCACTGCCGT | 11252 |
| rs750652036 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882778 | ACGGGGTGGGGGCTG[C/G]CTTCCGCCTGGCAGC | 11252 |
| rs750656036 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968750 | GGGCAAATGTGTCTA[C/T]CAATGTCCTGGAGCT | 11252 |
| rs750661661 | snp | G/T | 1.65767e-05 | 0.00287891 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876857 | GACAGAGTGAGCGCG[G/T]TGGGAGCAGAGGAAG | 11252 |
| rs750694480 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000623 | GTACACCCAAAAAAC[-/T]TTTAAGGAAGGTGAC | 11252 |
| rs750706890 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895057 | GAAGGTGGTTAGCCT[A/G]GGCAGCCTTCTCCAG | 11252 |
| rs750735281 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891217 | TGCGGGTCACTCAGC[A/G]CCGGCCATGGTGGGG | 11252 |
| rs750744868 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919015 | TCTTCCAGGTTGAGC[C/T]GACTACAACGACCTT | 11252 |
| rs750770515 | in-del | -/GG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923016 | TCCGGCAGAGGCAGA[-/GG]GGGAGTGAGTGTTGT | 11252 |
| rs750771655 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965182 | AGCCAGATGCAAAAT[A/G]GCACCCACTGTGTGT | 11252 |
| rs750780970 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927865 | GTGCTACAATTACAG[A/G]CGTGAGCCACCGTGC | 11252 |
| rs750784085 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973301 | ACTCTGTCACAGGTC[G/T]CGCCCACAAGGCAAT | 11252 |
| rs750819797 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006692 | TGATGGCGCATGCCT[A/G]TAATCCCAGCTACTT | 11252 |
| rs750820096 | snp | A/C | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895815 | GAGAAGGGCAGTATG[A/C]CAAACAGTTGGGACC | 11252 |
| rs750824599 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966077 | GAACCAAGATGTAAA[C/T]AGAGCCATCTTGGGC | 11252 |
| rs750834553 | snp | C/T | 1.66192e-05 | 0.00288259 | missense | PACSIN2 | GRCh38.p7 | 22:42879147 | CTCCGGCTGAGGGTT[C/T]GATTCAGGTCTGCGG | 11252 |
| rs750851888 | snp | A/T | 1.65592e-05 | 0.00287738 | missense | PACSIN2 | GRCh38.p7 | 22:42891086 | TCGAAGTCATCGTTC[A/T]TCAGTGAGGCCTTCA | 11252 |
| rs750887021 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998718 | ACCCTCAAGCCTGGA[C/T]CCAAGGCCCTAAATG | 11252 |
| rs750922626 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915789 | CCACTTCAGTTCTTG[A/G]GCTGGAATAATTCAC | 11252 |
| rs750943210 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901053 | CCCAGGAACCCCAAG[C/T]CTGTAAACTTCTAGG | 11252 |
| rs750948951 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975911 | CTGTAAGACAGACAC[A/G]AGAAAAAGACCCACT | 11252 |
| rs751003345 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964113 | AGCCCGCGGCAGTCA[C/T]TGTGTTTTACAAGGT | 11252 |
| rs751009739 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976757 | TCATTTCACAGATAC[C/T]CCATTTCGTCCTTCC | 11252 |
| rs751019339 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995024 | TGCCTCCTGGACTCC[C/G]TCTCAGGACCCTGCT | 11252 |
| rs751020770 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963776 | GTGCCTCCCATGGAA[C/T]GGGACCTGCTATGAA | 11252 |
| rs751022947 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952477 | GATTCTCCTGCCTCA[A/G]CCTCCTGATTAGCTG | 11252 |
| rs751068678 | in-del | -/AATA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956982 | GAATATTCTATACTT[-/AATA]TATAGTGAAAATATA | 11252 |
| rs751068783 | in-del | -/ATAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989884 | TATATATATATATAT[-/ATAC]ACACACACACACATA | 11252 |
| rs751071897 | snp | C/T | 3.30126e-05 | 0.00406266 | missense | PACSIN2 | GRCh38.p7 | 22:42884446 | ACCTCCCGGAAGAAG[C/T]GAAGGCGTTTCTCCT | 11252 |
| rs751092988 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925954 | CTGGAAGAATGGGGT[C/T]TCTTGCTTGTCTCTA | 11252 |
| rs751108792 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948418 | AAGCGCTATCTAGAA[A/G]TGAACTACCTAAATA | 11252 |
| rs751110147 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987220 | ATTTTAACTATCTCT[C/T]TGAGCCTCCATTTCA | 11252 |
| rs751143330 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004329 | TTCAGAACATGGGGG[C/G]CTGTGCAGACAGCCC | 11252 |
| rs751152036 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904221 | CTCTGCTCCCTTGGT[A/G]CGTGTTACACAGATG | 11252 |
| rs751152217 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928178 | CCCTTGAGAAAGGAC[A/G]GGAACACACCCGGAG | 11252 |
| rs751157686 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973959 | AGCCTTAACTTGTAG[C/G]CTGATACAAATGCCA | 11252 |
| rs751192489 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873118 | GGATAACACAGAAAA[C/T]AGAACGGACAGGAAA | 11252 |
| rs751193279 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975611 | TGTGTATAAGTATTC[-/T]TTTTTTTTTTCCCTT | 11252 |
| rs751221348 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899758 | TCCCTGGGGAATGCA[C/G]AGGTAAGCACGGGGC | 11252 |
| rs751248087 | snp | A/G | 3.31581e-05 | 0.00407161 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876297 | ATCGTCTGACCAGTC[A/G]GTGGGATAGCTCTGG | 11252 |
| rs751252937 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963221 | CCCACAATGTACAGG[A/C]TGAGCAGAAGTGCAA | 11252 |
| rs751263476 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974864 | GAGAAGGAACAACAA[A/C]AACAACATAAGCTTT | 11252 |
| rs751284704 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931381 | AGCTGCTTTCCACCC[A/G]GGGAAGTGAGGAAAT | 11252 |
| rs751352279 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969755 | ACCAGCCTGGGCAAC[A/G]TGGAAAGAACCCATC | 11252 |
| rs751354827 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962996 | AGTGATACAGCTGCC[C/T]GACCACTCTTTAGGT | 11252 |
| rs751368353 | snp | A/G | 3.35796e-05 | 0.0040974 | missense | PACSIN2 | GRCh38.p7 | 22:42893486 | TGCCTCCAGCGCCGG[A/G]CCCACTCAGTGAGCT | 11252 |
| rs751374000 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959448 | AAGCAAAGGTGCAAA[A/G]TTATTGCATCTATTT | 11252 |
| rs751396339 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932268 | TTCCCTGAGACAAGC[A/G]TATGGCCGGCTCCCC | 11252 |
| rs751396905 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989159 | GCTGGGATTACAGGT[A/G]TGAGCCACTGCACCT | 11252 |
| rs751408321 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940740 | AAGTCACAATTTAGG[A/T]GGCTCAAAAAGAATA | 11252 |
| rs751425021 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885985 | GAAGCCCAAGACACA[C/T]AGCTGTGGGTTCAGC | 11252 |
| rs751447604 | snp | A/G | 8.31539e-05 | 0.00644748 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893578 | CAGGCGGTGGCCATC[A/G]TCGATCCGCTTCACA | 11252 |
| rs751463000 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869992 | GCTGGTGACGGCGGC[A/G]GGCACTGCTGAGTCA | 11252 |
| rs751493378 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906545 | CGACAAAGTCTATCT[A/G]AACCACAATGGAAAT | 11252 |
| rs751509186 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915020 | AGGCACGTGCTGCCA[G/T]GCCCAGCTAATTAAA | 11252 |
| rs751536518 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975531 | AAATGAAATTTGCAG[-/AT]ATTACTTATGAGTCT | 11252 |
| rs751545549 | in-del | -/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872330 | GGCCTGTGTGCTTCT[-/G]GTTGGTAACTCACTG | 11252 |
| rs751554412 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42949053 | ATCCCAGCACTTTGG[A/G]AGGTGGAGGTGGAAG | 11252 |
| rs751571741 | snp | A/G | 3.37855e-05 | 0.00410994 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884377 | TGTTTTAGCTCAAAG[A/G]AAACTTACCCAGCCA | 11252 |
| rs751584554 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992934 | TCTGGGAGGCTGAGG[C/T]GGGCAGATTGCCCGA | 11252 |
| rs751604971 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937445 | AGCTTAAACGGGCAC[C/T]GAAGACAAAACAAAA | 11252 |
| rs751643802 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016845 | TACATCGCAATTCCA[C/T]GCCCTATAAAAATAT | 11252 |
| rs751647430 | snp | C/T | 0.000115993 | 0.00761466 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911999 | GGCCACTTCATTCAC[C/T]GGAAGAAAGCAGGTG | 11252 |
| rs751688184 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955192 | CCTCAGAGACCAGAA[C/T]TCAATCCTAACCGTC | 11252 |
| rs751729804 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899374 | TCACTTGCAACCTCT[A/G]CCTCCCGGGTTTAAG | 11252 |
| rs751731548 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923055 | CAGCACCCAACAAAG[C/T]GGAAGCTCACATGCT | 11252 |
| rs751750388 | snp | A/G | 1.65589e-05 | 0.00287736 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876964 | AGGGGTTGTAGCTGG[A/G]CTGTGACTGCGCAGA | 11252 |
| rs751757741 | snp | A/G | 0.000116166 | 0.00762034 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888615 | GACACGGTGACACTC[A/G]ACGTGTAAAAACAAG | 11252 |
| rs751765322 | snp | C/T | 1.66045e-05 | 0.00288132 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877056 | CAGCTCTGCAGGGGC[C/T]CGTGAGGGTCCTGGC | 11252 |
| rs751770535 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884712 | CAAGTTCAAGTCCCA[G/T]TTCCTCCACTCCTGC | 11252 |
| rs751774240 | snp | C/G/T | 3.31193e-05 | 0.00406925 | missense | PACSIN2 | GRCh38.p7 | 22:42888735 | CCTTGCTGTTGGCTT[C/G/T]TCGTGAGATAGCCAG | 11252 |
| rs751775938 | in-del | -/AAAC/AAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983498 | CATCTCAAAAAAAAA[-/AAAC/AAC]AAAAAAAAAACAGAT | 11252 |
| rs751809634 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877255 | ACCTGGAGACAGTCC[A/G]TCCAGAACAGGGGCC | 11252 |
| rs751821756 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897476 | TAGGTAGAAACTGAA[C/T]ATAAGCATGCTTTCT | 11252 |
| rs751860439 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880787 | CACCCTCCAGGAGAC[A/G]GACTGTCAAATAGTC | 11252 |
| rs751861627 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948365 | CCCACCATAAGAATG[-/C]TAGGTAAGCATGGAC | 11252 |
| rs751901413 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928882 | AAATTTGCCATTAAA[C/T]AGCAATGGGACATTG | 11252 |
| rs751922026 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974331 | CCCAGAGCATTCACC[-/T]GTTAATTAGATATGA | 11252 |
| rs751940931 | in-del | -/TCC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903875 | CACTGACTGGCCGTA[-/TCC]TCTGTTCCTGAAACC | 11252 |
| rs751973087 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916858 | AAAGTGATAGCCATT[G/T]TTCTTAGAATCACCA | 11252 |
| rs751983270 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890688 | CCACTGCACTCCAGC[C/T]TGGGAGAGAGAGTGA | 11252 |
| rs751984171 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944908 | TTCAAGACCAGCCGG[G/T]CCAACACAGTGAAAC | 11252 |
| rs752007135 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965306 | TCAAAGGGACACAAG[G/T]AAATTTTGGAGCAAT | 11252 |
| rs752064608 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936049 | AACCCCGTCTCTACT[-/A]AAAAAAAATACAAAA | 11252 |
| rs752065462 | snp | C/G | 1.66877e-05 | 0.00288852 | missense | PACSIN2 | GRCh38.p7 | 22:42876141 | AGCCCACCTACCAGC[C/G]TTGAAGCTCAGCTCA | 11252 |
| rs752082209 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006876 | TTCTCAACCAAACAC[A/G]TAAATGCAGGTTAAG | 11252 |
| rs752099617 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892230 | AGCCACAACGGAGCC[A/G]GGGCAGAAATCGAGA | 11252 |
| rs752103468 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977638 | TCACCCAAATCTCAC[A/G]GCAAATTGTAATCCC | 11252 |
| rs752115968 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961267 | AACACAAAACGAAGT[-/A]GGTTAAAAATCTCTT | 11252 |
| rs752130800 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939240 | TGGACTGATTTTTAC[A/C]GCAATATTTTTTTAG | 11252 |
| rs752132680 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997419 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT | 11252 |
| rs752156721 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902123 | AACAAACTGCCATGC[A/G]ACTGTCCCTCATGGA | 11252 |
| rs752183386 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984612 | AAAGGTTCCTGGTGC[A/C]AAAACTACTCCCTTT | 11252 |
| rs752201010 | snp | C/T | 3.31757e-05 | 0.00407269 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876849 | GGAAGAGAGACAGAG[C/T]GAGCGCGGTGGGAGC | 11252 |
| rs752204251 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006762 | GGAGGGTGCAGTGAG[C/T]CGAAATCGCACCATT | 11252 |
| rs752211954 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905277 | AGAAGGAAAGGTGAC[C/G]TCATTCATCCACCTT | 11252 |
| rs752229669 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967751 | AAATTAGCCGGGCGT[A/G]GGGGTGGGCGCCTGT | 11252 |
| rs752270037 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915185 | AGATTTAAGAGCCCA[C/T]TAAGTGCCAGGAGCC | 11252 |
| rs752285032 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963880 | TCTACTGGTCTGTCA[A/T]CGCTCTAATACTATA | 11252 |
| rs752300714 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948039 | CGGGGACACATAGAG[A/G]GTCCAGAAAGGGTGC | 11252 |
| rs752334092 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889483 | TAGCAAAGGCCTCAT[G/T]AGACACAGACAGTTT | 11252 |
| rs752368347 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963902 | ATACTATACTGCCTT[-/A]AAAAAAAAAACAGCT | 11252 |
| rs752372125 | snp | C/T | 3.32513e-05 | 0.00407732 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879152 | GCTGAGGGTTCGATT[C/T]AGGTCTGCGGACCAC | 11252 |
| rs752401589 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958659 | ACATACTATATACCT[A/T]GGGGGTTTCTAGAAA | 11252 |
| rs752411861 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900925 | CAAGTCAACATGAGA[-/T]GATGCGTGTGCTTCC | 11252 |
| rs752420359 | snp | C/T | 0.000118033 | 0.00768131 | missense | PACSIN2 | GRCh38.p7 | 22:42891171 | CCTTCTCCACGGTCC[C/T]GTACTGGGGCCCTGT | 11252 |
| rs752425747 | in-del | -/TCTG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902696 | CGGCTCACCACAACC[-/TCTG]TCTGCCTCCTGGGTT | 11252 |
| rs752459194 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997222 | CCAGTGCCTAGAACC[A/G]TGCCTAGCACATGGC | 11252 |
| rs752465953 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933248 | CCAACTTTCCTTAAA[C/T]CCTGAACAACTCTTT | 11252 |
| rs752468169 | snp | C/T | 3.3264e-05 | 0.0040781 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893585 | TGGCCATCGTCGATC[C/T]GCTTCACAGTCCGCT | 11252 |
| rs752501729 | snp | C/G | 1.67528e-05 | 0.00289415 | missense | PACSIN2 | GRCh38.p7 | 22:42884387 | CAAAGGAAACTTACC[C/G]AGCCACATTGGACAG | 11252 |
| rs752503525 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881530 | ACGCCACGTGCTTAA[A/G]CCTCAGGGGCACCAG | 11252 |
| rs752548169 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960944 | CAAAAACAGACAGGA[A/C]ACAAATATTTCAAGG | 11252 |
| rs752548350 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949128 | TGGGATCCTGTCTCT[A/G]TAAGGACAAAACATT | 11252 |
| rs752550868 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011991 | CTCTACTATAAATAC[A/G]AAAATTAGCCAGGCG | 11252 |
| rs752557857 | snp | A/G | 1.70502e-05 | 0.00291972 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893643 | CAGCTGGGAGGCAGG[A/G]GGCTTGGGGCAGCCT | 11252 |
| rs752561785 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988274 | ATTCACATTCACTGC[-/T]TAGGACCCTCACAGT | 11252 |
| rs752600418 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002928 | AATAATACAATTATA[A/C]CAATGTCAGTTATTG | 11252 |
| rs752602039 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001883 | ACTGCTCCCCACCTG[A/G]AGCCCCTCTCTGTCC | 11252 |
| rs752626471 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906199 | GTGTCCCAGCCCCAA[A/G]CTCAGGCCAGGCATG | 11252 |
| rs752632775 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008289 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 11252 |
| rs752689680 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939377 | TAAAAAGGACAAAAA[A/T]GACACTTTTTCAAAT | 11252 |
| rs752698455 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955925 | CCCCAAAACTGTCAT[-/G]TGCTTCATTTATTTT | 11252 |
| rs752700759 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932400 | ACATACCACTACCTC[A/G]GTTTTTACCTGTGTA | 11252 |
| rs752710905 | snp | C/T | 1.66272e-05 | 0.00288328 | missense | PACSIN2 | GRCh38.p7 | 22:42876326 | GGGTCTTCTCGTAGC[C/T]GCTCACACTGCAAGA | 11252 |
| rs752715406 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978699 | CTGCAGACGTTCAGG[C/T]GGACTCAGATCTGAG | 11252 |
| rs752733149 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896687 | GTTTAACAAAACTGC[C/T]GAACTGCTACCCAAA | 11252 |
| rs752777018 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903043 | CCCGGCGCTTCTGCC[A/G]CATTCCTGAGAGAGT | 11252 |
| rs752777370 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892560 | TGCAGCAGGTGGAAA[C/T]GAAATGACGACACTG | 11252 |
| rs752791259 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976431 | CAGACTGGCTCCTCT[A/C]CCCAAAAGCCTGACA | 11252 |
| rs752866852 | snp | A/G | 3.32165e-05 | 0.00407519 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877058 | GCTCTGCAGGGGCCC[A/G]TGAGGGTCCTGGCAA | 11252 |
| rs752867245 | snp | A/G | 2.54527e-05 | 0.00356731 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890886 | GGTGCAGGAGGTGGT[A/G]CTGCTAGTGGGGTGC | 11252 |
| rs752881776 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926587 | CTCTCCAATATCTCT[-/G]TTAAGAAGAAAAGAG | 11252 |
| rs752891298 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992948 | GCGGGCAGATTGCCC[A/G]AGCTCAGGAGTTTGA | 11252 |
| rs752916694 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886760 | GCTCTAGGCACACAA[A/G]GACCTCTCATATCCT | 11252 |
| rs752949272 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988086 | AGGTTGCTGTGAGCC[A/G]AGATCGCACCACTGC | 11252 |
| rs752950291 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886036 | TGCTGAAGTGACACA[A/G]AGCAGCCCCATCTCA | 11252 |
| rs752956842 | snp | A/C/G | 3.32714e-05 | 0.00407858 | missense, stop-gained | PACSIN2 | GRCh38.p7 | 22:42879073 | TACTCGGCAGAGACT[A/C/G]GTCGCCTGTCTGGTT | 11252 |
| rs753071097 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907356 | GTGGAGACTGAGGAG[C/T]TGATGCCTTAATCCT | 11252 |
| rs753071443 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946431 | GCAGCAATGTACCAC[A/G]GGCTCACCCACTACT | 11252 |
| rs753073198 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918750 | CCACCTGCCAGGGAG[A/G]CTGGAGCCTCAGGGC | 11252 |
| rs753078819 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991898 | CCTAAATGTAAAACA[C/T]AAAACTATAACATTT | 11252 |
| rs753099403 | snp | C/T | 3.32607e-05 | 0.0040779 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876153 | AGCCTTGAAGCTCAG[C/T]TCATCATGCTCCTGC | 11252 |
| rs753126121 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014211 | CGGATTTCTGATTCA[C/G]TGAGTCTGGGGAAAC | 11252 |
| rs753128790 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934696 | GCCCACCACTGTCCC[A/G]TTATAGTTCCTCTAT | 11252 |
| rs753188494 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881136 | TGCTCGGCAGCAGGG[C/T]CCACACTGTCATTTG | 11252 |
| rs753197460 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967526 | AACTTTGTAACAGAA[G/T]AATTATACTGTTGGT | 11252 |
| rs753232929 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877084 | GGCAACTCCTAGCTG[C/T]AGGATCTCAAGAGAC | 11252 |
| rs753267031 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013848 | CTGAGCAGCCTACCC[C/G]CTTAACCACAAAAAC | 11252 |
| rs753269159 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918002 | AACTGTATTTAAATA[C/T]AATGTTTACTGCACC | 11252 |
| rs753280751 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986692 | ACATCAGTGACCACT[C/G]AGAGGGGGCTTTTGT | 11252 |
| rs753281877 | snp | A/C | 1.65597e-05 | 0.00287743 | missense | PACSIN2 | GRCh38.p7 | 22:42888743 | TTGGCTTCTCGTGAG[A/C]TAGCCAGCTTCTCCT | 11252 |
| rs753289665 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986378 | CTCGTGAGTATCAAT[C/G]AAGGGCAGCATTCAT | 11252 |
| rs753299204 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956374 | GGAGGAGACGTCAGG[C/T]AGACACAACCTGTTA | 11252 |
| rs753350984 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897837 | GTGAGGCCAGGAAAA[C/T]AATTCCAGGCACAGG | 11252 |
| rs753365468 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965465 | GAAGGTGAGAAAACA[A/G]GAGAAAAGGAAGAAA | 11252 |
| rs753367845 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933608 | TCCTATACTCTCAAC[C/T]GTGGCGCCTAAAGGG | 11252 |
| rs753406012 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906302 | ATTACTGGGTAGAGA[C/T]TGGGCAGCAAAGGCT | 11252 |
| rs753460665 | snp | C/T | 1.71246e-05 | 0.00292609 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893454 | TGTGCCGGGGCCCCA[C/T]ACCTTTCTCCACGAG | 11252 |
| rs753467686 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013019 | CTGGTCTCTAAGTTC[A/T]GACCTCAGGTGATCT | 11252 |
| rs753474143 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880676 | AGAAAGGCATGGTCC[C/T]GTAACAGCTGCAAAT | 11252 |
| rs753495262 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916635 | TTCCTCCCCCAACTG[C/T]TTGCACACCTTGCAG | 11252 |
| rs753517191 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985476 | CCCCCACTGGCCTCA[C/T]TTCTCTCCACATGCA | 11252 |
| rs753519528 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877208 | GGTCCAGGAGCCTAG[A/G]AGAGGACTTGGTTTC | 11252 |
| rs753529133 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892224 | AGGGAGAGCCACAAC[A/G]GAGCCGGGGCAGAAA | 11252 |
| rs753548652 | snp | A/G | 1.66051e-05 | 0.00288137 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42882259 | GTCCTCCACTGCATC[A/G]GCTGCTCTGATGCTC | 11252 |
| rs753552746 | in-del | -/GTAGGTAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886448 | TAGGTAGGTAGGTAG[-/GTAGGTAT]GTATGTACCTACCTA | 11252 |
| rs753589784 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912196 | TAGTGGTTTTTAAAT[C/T]CCCAAGGTAAAGAAA | 11252 |
| rs753591346 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996534 | AAGACTCTGCCGCAA[-/AA]AAAAAAAAAAAAAAA | 11252 |
| rs753649909 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944824 | GGACTGTAGCTGGGC[A/G]CGGTGGCTCACGCCT | 11252 |
| rs753691780 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984588 | CAGCGGGTTGACAAC[A/G]CCTGCTGCAAAGGTT | 11252 |
| rs753694505 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919938 | GAGACCACCATCTCT[-/A]AAAAAAAAAAAAAAG | 11252 |
| rs753696573 | snp | C/T | 1.64963e-05 | 0.00287192 | missense | PACSIN2 | GRCh38.p7 | 22:42884519 | TGTACTGGGGTGTGC[C/T]CTGGTCGAGTTCCTT | 11252 |
| rs753717609 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973034 | TTTTATGGCTGGGGT[A/C]AATACGGAAGTAAGA | 11252 |
| rs753751066 | snp | A/G | 3.3162e-05 | 0.00407184 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876854 | AGAGACAGAGTGAGC[A/G]CGGTGGGAGCAGAGG | 11252 |
| rs753764411 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961231 | TGTTCAGTTAAAAAC[A/G]GCCATCTAGTCTTAC | 11252 |
| rs753792219 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002986 | CTCCAGATCTCTCCC[A/G]TCTACAAACTGGATG | 11252 |
| rs753832418 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918893 | GCTTGCAGCACCCTC[C/T]CAGCTGAAGAAACAC | 11252 |
| rs753836689 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998978 | CCAGCTCCCCATCCT[G/T]CTGAGAGCCACCTCC | 11252 |
| rs753838396 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929863 | GATCAGATGCCACCT[C/T]TTTCATAAAGACTTC | 11252 |
| rs753847193 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004223 | CTCTCTGAGCTTAGG[C/T]TTACTGATGGATCAA | 11252 |
| rs753859220 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870345 | GGGAGGAGACCCAGC[C/T]GGCCAGCCAGACGTG | 11252 |
| rs753870098 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956612 | TAGGATACTGGGGGA[A/T]GTTTCTTCATAGTCT | 11252 |
| rs753930329 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999754 | ACTCCCTAACTTGCT[A/G]GGGAGACAGGGCCAC | 11252 |
| rs753971415 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976983 | GCTAGAGTAAACCTT[C/G]TTTGGTCATGAAAAA | 11252 |
| rs754004938 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903970 | TTTGATCATTTAAAA[A/G]CATGAATCCCAGATT | 11252 |
| rs754009723 | snp | C/G/T | 0.000212509 | 0.0103062 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871328 | TGGGCCCGCCGCCTC[C/G/T]GTCCCCCCGCTGGCC | 11252 |
| rs754015061 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009072 | CGGCAGATGAACAAA[C/T]AGTTTCCTCTACGAG | 11252 |
| rs754016189 | snp | A/G | 1.73195e-05 | 0.00294269 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893659 | GGCTTGGGGCAGCCT[A/G]TCCTTGGCTGTGGCA | 11252 |
| rs754073996 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978891 | CCTTCAAAACAATTG[C/T]TTCTCCCCTGGCTTC | 11252 |
| rs754096199 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967868 | ACTCCAGCCTGGGCC[A/G]CAGAGCGAGACTCCA | 11252 |
| rs754122955 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877962 | GCCACCAGGGTGATC[C/G]TGAGTGGCCAGTAAC | 11252 |
| rs754153309 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900947 | TGTGCTTCCAGCCAG[C/T]CCTGTGGGCGCCAGC | 11252 |
| rs754154367 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013481 | AATCAAGAGAGATCC[A/G]AGTTGCACTGGCACA | 11252 |
| rs754174869 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937174 | AGAGAAATAAGCGAG[A/G]ATGAGATAGGGAGGA | 11252 |
| rs754179282 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940375 | CGCTGTGCAAAGCAG[C/G]GGGTCAGCATGTGTT | 11252 |
| rs754200952 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935742 | GAAACACACTGGTCC[C/T]GAGGGAACACAGGTG | 11252 |
| rs754210366 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909391 | GCTTTCTTTGGAAAA[A/G]TGTCCTTCCATGGGA | 11252 |
| rs754210477 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899933 | AGATGCTAACAAAAG[C/T]TGTAACATTAGAAAT | 11252 |
| rs754212917 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011061 | TACTCATCTGAACAC[C/T]AAAATTCTGCAGAAA | 11252 |
| rs754227683 | snp | G/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017387 | ATCTTTGTAGAGACA[G/T]AATCTCGCCATGTTG | 11252 |
| rs754284663 | snp | A/C/T | 8.27959e-05 | 0.00643359 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888766 | CTTCTCCTCTTTGCA[A/C/T]GCTGCATGGTGGGCT | 11252 |
| rs754346132 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000524 | GTTATGTTAAACTAT[C/T]TCTAAATTTCGTGAA | 11252 |
| rs754347757 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873200 | AGTTTGCTTTTGACA[A/G]TTTACTTGGATCTGG | 11252 |
| rs754351042 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896096 | GTGGACAAACATATA[C/T]CACTGTCTACCACCT | 11252 |
| rs754426736 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974187 | TGTCGACTCTGCTTC[C/T]GGTTATCCGCCATCC | 11252 |
| rs754426869 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990038 | TATGTATATATATGT[A/G]TATATATATATATAC | 11252 |
| rs754429620 | in-del | -/GA | 1.67898e-05 | 0.00289735 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879190 | CAACAGGTGCCGAGG[-/GA]GAGAAACCAAAGGTT | 11252 |
| rs754440480 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904257 | AAGGCCCCGCGACAC[C/T]CTACATGGCGTTCAC | 11252 |
| rs754444599 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42995114 | GGGCCCCAACTGCCA[A/G]GAAGCAAGACTGGAC | 11252 |
| rs754496361 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943610 | GCTTGGGGTTGGGTG[-/T]TTTTTTCTTTCTTTT | 11252 |
| rs754533087 | snp | A/G | 3.31312e-05 | 0.00406995 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876228 | GGTGGCGTCGTCGTC[A/G]AATGGATTCGAGTCC | 11252 |
| rs754539418 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977844 | CCACCATGATTGTAG[-/T]TTTCCTGAGGCCTCC | 11252 |
| rs754553127 | snp | C/T | 3.32193e-05 | 0.00407536 | missense | PACSIN2 | GRCh38.p7 | 22:42876320 | AGCTCTGGGTCTTCT[C/T]GTAGCTGCTCACACT | 11252 |
| rs754553532 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878289 | CAGCGTGCAAAGCAG[C/T]GGAATGACGACAGCC | 11252 |
| rs754558591 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989502 | AAACTCCATCCCCCT[-/C]AAAAAAAAAAAAGGC | 11252 |
| rs754596712 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887500 | GCCTCCCCTCTGCCC[A/G]TGTCCTCTTCCTGGA | 11252 |
| rs754671658 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932344 | CACCACCACCAACTC[C/T]AGCCTGTTACCTTCT | 11252 |
| rs754671932 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964191 | GTGGGGCCAAGGTGC[A/G]CAGATCACTTGAGGT | 11252 |
| rs754718866 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926034 | CACATTAAGATAGTG[C/T]TTTGCACCATTAGCA | 11252 |
| rs754719251 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887166 | GGAGGCACCTGGGCT[G/T]CTTCAAAAGCCCAGA | 11252 |
| rs754722616 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011948 | TCAGGAAATCGAGAC[C/T]ATACTGGCCAACACG | 11252 |
| rs754729833 | in-del | -/ATACACACACAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889383 | TTTTTACACACACAC[-/ATACACACACAT]ACACACACACACACA | 11252 |
| rs754743871 | snp | A/G | 1.67649e-05 | 0.0028952 | missense | PACSIN2 | GRCh38.p7 | 22:42893490 | TCCAGCGCCGGGCCC[A/G]CTCAGTGAGCTGCTG | 11252 |
| rs754746259 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920360 | TAAACTTTTAGAATG[G/T]GGTGGTGTGTGCTGA | 11252 |
| rs754756519 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000995 | CTAAAAAGCAGAAGG[A/C]ACTTGAAGGGAGAGC | 11252 |
| rs754795487 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883335 | AATGGTGGCAGAGCA[A/G]CAGCGGTGCAGTAAC | 11252 |
| rs754803480 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955806 | TAACAAATGTTTCTG[-/T]CTTCCAAATCAATAG | 11252 |
| rs754807848 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990651 | ATGGGAGAAATGCAA[A/G]AAGTTCAGGAGTGTG | 11252 |
| rs754809988 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001832 | AATTCTAGGGAGGGG[A/C]CCCAGGGGTAAGCAC | 11252 |
| rs754833385 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934348 | ACCTTCAAGGCACTG[-/T]TGTGTGTGCAGATCG | 11252 |
| rs754878451 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959481 | AAAGGAAACACGCAC[A/G]TATGTTCTAAAACCA | 11252 |
| rs754885065 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010822 | AAGCAAACAGATGAA[A/C]ATGCATTTATGGGAA | 11252 |
| rs754885082 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905162 | GACAGCACAAAACCC[A/C]GAAGTGCTAAATTCC | 11252 |
| rs754905671 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984483 | ACTGGTCCCATCTTG[C/T]ATCTCCCCAGACTGG | 11252 |
| rs754921750 | snp | A/C | 0.00290578 | 0.0380059 | splice-donor-variant | PACSIN2 | GRCh38.p7 | 22:42884384 | GCTCAAAGGAAACTT[A/C]CCCAGCCACATTGGA | 11252 |
| rs754955559 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958627 | CAAAACTGATGGGCC[C/T]GATTAAGGTCGGACA | 11252 |
| rs754976484 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899821 | ACTACGCCGACACAC[C/T]GACCCAGAACAGAAA | 11252 |
| rs754978062 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931411 | TGGCTTCCAAGCCAG[C/T]GACACCAAGGTGAAC | 11252 |
| rs754988496 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927524 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 11252 |
| rs755010910 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923309 | AAAATGCAAGGCAGA[A/C]CACATTGCTGGTCTT | 11252 |
| rs755067762 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918400 | AGAAGTGGGATAAAC[C/T]ACCATCCAAGCAGCT | 11252 |
| rs755067971 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891391 | GAAAATTGGGGGATT[A/C]CATGCCTTTCCTTTA | 11252 |
| rs755073091 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977687 | CCTGATGGGAGGTGA[G/T]TAGATCATGGAGGCG | 11252 |
| rs755087630 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006145 | GCCTTCTTTCTGTCA[C/T]GTGAAGCTATAAGAA | 11252 |
| rs755096011 | snp | A/T | 1.65921e-05 | 0.00288024 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888616 | ACACGGTGACACTCG[A/T]CGTGTAAAAACAAGT | 11252 |
| rs755140790 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873123 | ACACAGAAAATAGAA[C/T]GGACAGGAAAGCTTT | 11252 |
| rs755145417 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965348 | GTCTTGACTGAGTCA[C/T]ACAGGTGTTTCCACT | 11252 |
| rs755218290 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875294 | ACTATAGGTATGCAA[C/G]ACCACGCCCAGCTAA | 11252 |
| rs755233504 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976803 | CAGTATTGTAATTGT[C/T]CTGCCAATTTTATAG | 11252 |
| rs755253208 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909880 | GTCGCCAAGGGCACC[A/G]CAGGAACAGACATTG | 11252 |
| rs755289267 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930708 | TGGGTCAGTGGGAAA[C/G]TTTAAGAATTAAAAA | 11252 |
| rs755297771 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985651 | GAACAGCCCCTCCAA[A/C]AGACACACACACAGA | 11252 |
| rs755307767 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871181 | CCCTCCAGCTGCACT[C/T]GGAAAGGTGCCGAGT | 11252 |
| rs755316429 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880954 | TCAGCCAAGACTTCC[C/T]GGTGTGTGGCTCCAG | 11252 |
| rs755325130 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945006 | AGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC | 11252 |
| rs755336044 | snp | C/T | 0.000132578 | 0.00814071 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882160 | TTCCAGGCTGATGAG[C/T]TCATGGGCACACCCT | 11252 |
| rs755350396 | snp | A/G/T | 0.000133966 | 0.00818331 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871514 | GAGAGGTATGACACC[A/G/T]ACGGTGGGCTACAGA | 11252 |
| rs755368640 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998728 | CTGGACCCAAGGCCC[G/T]AAATGAGAACAAGCA | 11252 |
| rs755387367 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971334 | GCAAGTGATCTGCCC[A/G]CCTCAGCCTCCCGAG | 11252 |
| rs755408428 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966244 | GTGTGGTGGTGTGCA[C/T]CTGTAGTCCCAGCTA | 11252 |
| rs755416776 | snp | A/C | 1.65767e-05 | 0.00287891 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912060 | TTCTACTCCAACGGA[A/C]TCATCATATGTGACA | 11252 |
| rs755473860 | in-del | -/C | 1.79648e-05 | 0.00299701 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882352 | GGCAGGGGCCAGCTA[-/C]CCTTTGTCCCAGCCC | 11252 |
| rs755486426 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875311 | CCACGCCCAGCTAAT[C/T]TGCTACTTTTGTTTG | 11252 |
| rs755508094 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955189 | GGTCCTCAGAGACCA[A/G]AACTCAATCCTAACC | 11252 |
| rs755558244 | in-del | -/AATG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908372 | TCCCAGAGCCTACTG[-/AATG]AAGGTAAGGGAGGCC | 11252 |
| rs755574505 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984618 | TCCTGGTGCAAAAAC[C/T]ACTCCCTTTAATCGG | 11252 |
| rs755583774 | snp | C/T | 4.98376e-05 | 0.00499163 | missense | PACSIN2 | GRCh38.p7 | 22:42884551 | AGGGACTTCTCATAC[C/T]TCTCTTTGGTCTAAA | 11252 |
| rs755609933 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945200 | GACTAGATGTACGCA[A/C]CGGCAATTACCAAGC | 11252 |
| rs755651822 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011091 | ATTCCTACAAAACTA[C/T]CCCAAGAACCACCAC | 11252 |
| rs755673346 | in-del | -/TTAAGT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013428 | TACCAAACTCTAGAA[-/TTAAGT]TTAAGTCCACACAAG | 11252 |
| rs755676409 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906216 | TCAGGCCAGGCATGA[A/G]CCTGACTGACTGACC | 11252 |
| rs755681792 | snp | C/T | 1.65627e-05 | 0.00287769 | missense | PACSIN2 | GRCh38.p7 | 22:42891105 | GTGAGGCCTTCACCT[C/T]GAGGTGCAGCTCGCT | 11252 |
| rs755693990 | in-del | -/GA | 1.65696e-05 | 0.00287828 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877015 | ATTAAGGGTGCTATG[-/GA]GAGAGAGAGAGCTTT | 11252 |
| rs755695804 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985391 | CTGTCTCCCACAAGC[C/G]ATTCCTGATGGGCTC | 11252 |
| rs755747695 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954590 | TAGAGACAGAGGACT[C/T]ACTATGTTGTCCAGA | 11252 |
| rs755765366 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953694 | AGAAACTAAAACTCC[A/G]AGAGGTTAAGTAATG | 11252 |
| rs755774117 | snp | A/G | 1.68624e-05 | 0.0029036 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891172 | CTTCTCCACGGTCCC[A/G]TACTGGGGCCCTGTG | 11252 |
| rs755785661 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927109 | GTCCCACCAGCCTCC[A/G]CTCTCCTCATTTAGC | 11252 |
| rs755798918 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004464 | ATTAAAGCATCACCA[C/T]GTGCGAGCTAAGTGG | 11252 |
| rs755815168 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922573 | TGGCCGCTCCACAGG[A/C]CTTGCACTGAGCACA | 11252 |
| rs755822354 | in-del | -/A | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873277 | GATTGAAAAGGAGTT[-/A]AGAAATTATAAACAA | 11252 |
| rs755833745 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914331 | TCTGCTTCCCAGGTT[C/G]AAGCAACTCTAGTGC | 11252 |
| rs755868374 | snp | A/G | 1.64955e-05 | 0.00287184 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884451 | CCGGAAGAAGCGAAG[A/G]CGTTTCTCCTCGAAC | 11252 |
| rs755880100 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921289 | ATTTGAACCCAGGAG[A/G]TGGAGGCTGCAGTGA | 11252 |
| rs755883670 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989497 | GAGTGAAACTCCATC[C/T]CCCTCAAAAAAAAAA | 11252 |
| rs755898836 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992983 | AGCCTGGGCAACACA[A/G]TGAAGCCCCGTCTCT | 11252 |
| rs755921367 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992295 | GGTGAGGATGTGGGG[G/T]AACTAGAACCCAGTG | 11252 |
| rs755922805 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875400 | TTTGCGACAGGGTCT[C/T]GCTCTGTTGTCCAGG | 11252 |
| rs755941337 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976955 | ATACCTCATGTTATG[C/G]TATCCTTGCATTGCT | 11252 |
| rs755958498 | snp | C/T | 1.66291e-05 | 0.00288345 | missense | PACSIN2 | GRCh38.p7 | 22:42876328 | GTCTTCTCGTAGCTG[C/T]TCACACTGCAAGAAA | 11252 |
| rs756009244 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001931 | CTTTGCAGACCCTGG[C/T]AAATGAGCCACCAGG | 11252 |
| rs756013211 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897698 | GCATGTACCTACTGA[A/G]GGACTCAGTGCTTGG | 11252 |
| rs756076585 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982553 | CTTCTGCCTTGGGAT[-/C]CTGTTGATCTGTGAC | 11252 |
| rs756080806 | snp | A/G | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959648 | TAATTGAACATTGCC[A/G]TCACGGAGCTCTAAA | 11252 |
| rs756081993 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935090 | CCGGCTAATTTTTTT[C/T]TTTTTTTTTTATTTT | 11252 |
| rs756161199 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929129 | GATCCAGGCCTGACG[A/G]CCGCCCTGTGCAACT | 11252 |
| rs756180769 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977078 | TGCAAATATATAAAC[-/AT]ATATATGCATTAATA | 11252 |
| rs756209884 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008161 | TACATCAGAAGTATT[C/T]TTTTAAAAAATAAAA | 11252 |
| rs756226931 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007048 | CACCCCTCCCCCATC[C/T]GCATCCCTGACTTCT | 11252 |
| rs756244274 | snp | C/T | 6.68863e-05 | 0.00578262 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42893506 | CTCAGTGAGCTGCTG[C/T]GCATACGCCTTCTCG | 11252 |
| rs756260590 | snp | A/G | 1.73516e-05 | 0.00294542 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878998 | ATGCAGATTGCCCAG[A/G]GCCCCCACCATGGAA | 11252 |
| rs756261783 | in-del | -/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017197 | TTTTTGGGGGTTTTT[-/G]TTTTGGTTTGTTTGA | 11252 |
| rs756266965 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915864 | GGTCTCACTGAACTG[C/T]GCAGTCAGAATCTAG | 11252 |
| rs756272237 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881271 | CAATAGCCCTGCGTG[A/G]ACAAAGTCACCATGT | 11252 |
| rs756277403 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955877 | TTCATGTGTCAGTTC[A/G]TAGCAGAGAAGATAG | 11252 |
| rs756280391 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977787 | CCTCACGCTCTCTGT[C/T]TCTCTCCTGCTCTGC | 11252 |
| rs756305529 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998761 | CCTGTTTTCGCACCC[A/G]AATGTTGCCTTTCAG | 11252 |
| rs756323286 | in-del | -/CATGC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001127 | TCAGCCCTATCAGTG[-/CATGC]CATGCCATGCCATAC | 11252 |
| rs756324810 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928238 | CACCTTGGCTAAAAA[A/C]TGTCGCTGCCTCTGA | 11252 |
| rs756331843 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966646 | CACCAATGTGATAGA[C/G]GGAACATGTTAATTT | 11252 |
| rs756348383 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902439 | TACTATGCCTCTATA[C/T]GTCTCCATCATCCAT | 11252 |
| rs756372354 | snp | A/G | 9.98004e-05 | 0.0070633 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893586 | GGCCATCGTCGATCC[A/G]CTTCACAGTCCGCTT | 11252 |
| rs756391889 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939426 | TTCAAACAGTAGTGT[A/G]AGAAGATGTACAAGA | 11252 |
| rs756421806 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950376 | AAATACTAGGAAAGA[C/T]AAGACAAAGTCATAC | 11252 |
| rs756431066 | snp | A/C/T | 3.32095e-05 | 0.00407478 | synonymous-codon, missense | PACSIN2 | GRCh38.p7 | 22:42876162 | GCTCAGCTCATCATG[A/C/T]TCCTGCCCCTCATAG | 11252 |
| rs756445109 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989816 | AAAAAACAAAACAAG[-/A]AAAGAAAAAAAAAAG | 11252 |
| rs756468030 | in-del | -/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990037 | ATATGTATATATATG[-/TA]TATATATATATATAC | 11252 |
| rs756472266 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899309 | TCTTTTTTTTTGAGA[C/T]GGAGTCTAGCTCTGT | 11252 |
| rs756481295 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934767 | GTTGTTAACCCTGGT[A/C]GATCAGACCATACTC | 11252 |
| rs756511781 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908181 | TCTGAGCTCTAAATG[C/T]ACAGACAGCTGACAG | 11252 |
| rs756535149 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004366 | ACTGACTCTGCACCC[C/G]CCACGCACATCCTCC | 11252 |
| rs756540508 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988190 | AGAACACAAAAGCAA[A/G]ACCATTTAGAAAATG | 11252 |
| rs756549576 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973972 | AGCCTGATACAAATG[C/T]CAGCTCACAGCCCAC | 11252 |
| rs756564791 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918786 | CATTGACCCTGATCT[C/T]TACCACATCCCCAAA | 11252 |
| rs756584582 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973316 | TCGCCCACAAGGCAA[C/T]CCCTCCTGAGCAACT | 11252 |
| rs756617812 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918047 | TTGCCTGGCAGAATC[A/G]TGGTGAGGGTCAACT | 11252 |
| rs756628437 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999631 | CAAGATCATGCCATT[G/T]CACTCCAGCCTGGGC | 11252 |
| rs756654688 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948868 | AGTGCTTTTATTTCT[-/A]AAAAAAAGTTCACAT | 11252 |
| rs756656472 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973332 | CCCTCCTGAGCAACT[C/T]CATTATTTCCACTTG | 11252 |
| rs756659934 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933614 | ACTCTCAACCGTGGC[A/G]CCTAAAGGGGAAGTG | 11252 |
| rs756707079 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870824 | TGGCTGAGTAACAGG[A/G]TAAGGGAATAGGGAG | 11252 |
| rs756708604 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885201 | GGGCAGCTAGAAAAC[A/G]TGTGAAATTCCTAAG | 11252 |
| rs756709036 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871272 | AACCATCATCTCTTG[C/G]AGGAAAAGGAGTGGA | 11252 |
| rs756735205 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871032 | TAATCAGTGGAACAA[C/G]ATCAGTGTAACCCAC | 11252 |
| rs756766401 | in-del | -/GGGGCG/GGGGCGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962775 | GAGCAAGGTGTGGGC[-/GGGGCG/GGGGCGG]GGGGGGGGGGGGCGG | 11252 |
| rs756812708 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899026 | TGCCTTTCACAAGGA[C/T]GCTGGAGAAGGTCTG | 11252 |
| rs756820257 | snp | A/G | 6.62921e-05 | 0.00575688 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882167 | CTGATGAGCTCATGG[A/G]CACACCCTCCTCTTA | 11252 |
| rs756821857 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973061 | AAGAACTTTGACAGG[A/G]CAGTCATATATCTGC | 11252 |
| rs756833236 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989502 | AAACTCCATCCCCCT[-/CA]AAAAAAAAAAAGGCC | 11252 |
| rs756857677 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882056 | ACTATAGCTATGCCT[-/A]AAAGGCTGCCTGATA | 11252 |
| rs756861330 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898154 | AGCTGCCCATCCTCC[A/G]GGTGGAGGATGCGGG | 11252 |
| rs756903656 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971037 | GGGTCTGCAGGCTAA[C/T]GCTAAGCTAAAAACA | 11252 |
| rs756914779 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906311 | TAGAGATTGGGCAGC[A/C]AAGGCTGCTTTCTGC | 11252 |
| rs756953245 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985380 | CCAGAGACTGGCTGT[C/T]TCCCACAAGCCATTC | 11252 |
| rs756999761 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940923 | AATTCACACAGTTCA[A/C]CCATCTAAAATGTAC | 11252 |
| rs757030006 | snp | C/T | 1.65086e-05 | 0.00287298 | missense | PACSIN2 | GRCh38.p7 | 22:42884525 | GGGGTGTGCCCTGGT[C/T]GAGTTCCTTCAGGGA | 11252 |
| rs757030388 | snp | C/G/T | 0.000233681 | 0.0108071 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876344 | TCACACTGCAAGAAA[C/G/T]GGGAGGCCACAGGGC | 11252 |
| rs757031165 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012123 | GCCTCCAGCCCGGGC[A/G]ACAGAGCGAGACTCT | 11252 |
| rs757048314 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978976 | ACTGATTATGCTCAG[A/G]TTAGCTGGTGACCTC | 11252 |
| rs757061121 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999321 | AACTCTCCCATTTCA[A/G]TAACATATAAATGTC | 11252 |
| rs757089486 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966733 | TTCTAGCACATCTCA[C/G]TTAAGATGTCACGCA | 11252 |
| rs757098681 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877250 | CTTGCACCTGGAGAC[A/G]GTCCGTCCAGAACAG | 11252 |
| rs757151667 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886298 | TCACCCTTAGGTGGA[C/T]TGTAATATTTTAGCA | 11252 |
| rs757162737 | in-del | -/TTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983966 | ACAGCACTTAGCACT[-/TTTTT]TTTTTTTTTTTTTTT | 11252 |
| rs757179512 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922729 | TTTACCATGTGAACA[C/T]CTACCATGTGCCAGG | 11252 |
| rs757184456 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961236 | AGTTAAAAACAGCCA[C/T]CTAGTCTTACCTTAT | 11252 |
| rs757239477 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950924 | AGTAGGTAATGTAGC[A/G]GCAGACAGCATTAAG | 11252 |
| rs757259449 | in-del | -/ACTAACCAGGCAAGGTGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011727 | ATTAAAAATACAAAA[-/ACTAACCAGGCAAGGTGG]CAGGCGCCTGTAATC | 11252 |
| rs757264025 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963102 | TTCTGATCTGGCTTC[C/T]GTCATCAAAGACTGG | 11252 |
| rs757301717 | snp | A/T | 1.73351e-05 | 0.00294402 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893663 | TGGGGCAGCCTGTCC[A/T]TGGCTGTGGCACAAA | 11252 |
| rs757302705 | snp | C/T | 0.000132696 | 0.00814436 | missense | PACSIN2 | GRCh38.p7 | 22:42891135 | TCACCCTCTCTGCCT[C/T]GGACATGAAGGCCAT | 11252 |
| rs757307330 | snp | A/G | 1.66763e-05 | 0.00288753 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893598 | TCCGCTTCACAGTCC[A/G]CTTGTAGTTCCCGAC | 11252 |
| rs757343934 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999780 | GCCACTGTGGGGGAC[C/G]ACCAGTGCTTTGAAG | 11252 |
| rs757357525 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893811 | TTAATAAGATCATAC[A/C]CATCAGTGAACGGGG | 11252 |
| rs757358031 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908268 | TCCTAAAATAAGTGG[C/T]GTCTGCCCTCCTAGC | 11252 |
| rs757358970 | in-del | -/CTG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000422 | CCTCCACCAATCACA[-/CTG]CTAACATGAGGCTTT | 11252 |
| rs757360038 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877569 | GCCTGCGGCACCGTC[C/T]TTTCTAGATAGAAAG | 11252 |
| rs757362193 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911318 | AGTAGGCTGAGGTGG[A/G]AGGATGGCTTGAGCC | 11252 |
| rs757382331 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918134 | CTATGGTGGGCATGA[A/C]CCCATCCTGAGTAGG | 11252 |
| rs757385075 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015359 | GGGAGTGCCTATTTA[A/C]TGGGCTGCGAGGGTG | 11252 |
| rs757388693 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894816 | TGACAGAAAAACGAT[C/T]TCTTTTCAGCCTTTT | 11252 |
| rs757409350 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918942 | GAGGCTTCTGAGAGC[C/G]ATTGTTTCTTCAAAA | 11252 |
| rs757424459 | snp | C/T | 6.63262e-05 | 0.00575836 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871384 | CTCCACATAATTTGC[C/T]GGGTATAGGCCAACT | 11252 |
| rs757428102 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967874 | GCCTGGGCCGCAGAG[C/T]GAGACTCCATCTCAA | 11252 |
| rs757435056 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882000 | GAAGGCCTTCGGTAA[C/T]GCCTGCAGCCCCCCA | 11252 |
| rs757445952 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009179 | AAGCCCCAGGATGGC[A/C]ACCAGGAGCCCCAGT | 11252 |
| rs757449034 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988332 | TGTGGGATGTGTGAG[C/T]GAGGGGTGGGGGGCA | 11252 |
| rs757454750 | in-del | -/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925885 | GGTCCCTGGGCCCTC[-/TA]TGTCACCAGCCTTGG | 11252 |
| rs757487564 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956622 | GGGGATGTTTCTTCA[C/T]AGTCTTAGAGAAGGT | 11252 |
| rs757502723 | snp | A/C | 1.65603e-05 | 0.00287747 | missense | PACSIN2 | GRCh38.p7 | 22:42888780 | ACGCTGCATGGTGGG[A/C]TTTCTTTGCTGCTTC | 11252 |
| rs757507925 | snp | A/C/T | 3.29855e-05 | 0.00406102 | synonymous-codon, missense | PACSIN2 | GRCh38.p7 | 22:42884454 | GAAGAAGCGAAGGCG[A/C/T]TTCTCCTCGAACTGC | 11252 |
| rs757522027 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989224 | AATTCTCGGCCGGGC[A/G]CAGTGGCTCACGCCT | 11252 |
| rs757525940 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945762 | TTGCCTCCTGCCTAA[A/T]CCTTAACAACGTCCT | 11252 |
| rs757583550 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937314 | GCAGCCCCAGCAAAA[A/G]GCAAGAGAGGCCCAC | 11252 |
| rs757592688 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929872 | CCACCTCTTTCATAA[A/C]GACTTCCTTTATTCC | 11252 |
| rs757593212 | snp | A/C | 1.73402e-05 | 0.00294445 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879007 | GCCCAGGGCCCCCAC[A/C]ATGGAACGGCCTCTT | 11252 |
| rs757598346 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889536 | AAAACAGAAGAGAAA[C/G]GAGATGTGACAAAAG | 11252 |
| rs757637586 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926214 | CATTTGATTCAACAA[C/T]GGGAAACAGCTTGCG | 11252 |
| rs757647489 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995264 | GAGCTCTGCTTCTGA[C/T]ATGAAGTGTGGCAAG | 11252 |
| rs757651373 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900957 | GCCAGCCCTGTGGGC[A/G]CCAGCAAGTCACAAA | 11252 |
| rs757651445 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887837 | GGGCAGAAAATCTCC[A/G]CTTCACAACAGAAAT | 11252 |
| rs757652377 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909431 | TTGCTACCTGCCTGG[A/G]AAGATGTGCAGTTGG | 11252 |
| rs757667627 | snp | A/G | 2.44442e-05 | 0.00349593 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890900 | TGCTGCTAGTGGGGT[A/G]CCAGGCAGAGCAAGG | 11252 |
| rs757695828 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964011 | GTGTGCAACCATCAC[C/G]ACCGTCAAGGGTAGG | 11252 |
| rs757704523 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899954 | CATTAGAAATGGGGA[A/G]GGGGCCTAGGTATCA | 11252 |
| rs757711872 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963307 | ACTCAAACCATGTGG[A/G]TTAAGGCGGAAGAAA | 11252 |
| rs757786886 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974188 | GTCGACTCTGCTTCC[A/G]GTTATCCGCCATCCA | 11252 |
| rs757811088 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997097 | AGGCTTGGACCCTCC[C/T]GCCCACTGAGGCTGG | 11252 |
| rs757834331 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004317 | TCCCTCAGAAACTTC[A/G]GAACATGGGGGCCTG | 11252 |
| rs757836895 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889466 | GGGAAGGAGGAGTTT[A/T]TTAGCAAAGGCCTCA | 11252 |
| rs757840638 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870442 | ATTAAAACAGTAGAC[A/G]AGTGCTTTAGATTCT | 11252 |
| rs757912168 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951148 | AAAATTCAAAAGGAA[G/T]ATAAGGCAGCACGTG | 11252 |
| rs757926842 | snp | A/G | 3.31483e-05 | 0.004071 | missense | PACSIN2 | GRCh38.p7 | 22:42876187 | TCATAGTCATACAGG[A/G]CCCGGACTCGCACTT | 11252 |
| rs757930516 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014032 | TAGCACAGCTTGCTC[A/C]CCTGACCAACCAACT | 11252 |
| rs757938004 | in-del | -/CTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923420 | CTTCAACTATTTCTC[-/CTT]CTTCTTCTTTTTTTT | 11252 |
| rs757968644 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963199 | GCAGCCAAGGTCCCT[A/G]CCCCGGCCCACAATG | 11252 |
| rs757985206 | snp | C/T | 1.70892e-05 | 0.00292306 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884365 | CAATGACGTGTGTGT[C/T]TTAGCTCAAAGGAAA | 11252 |
| rs757988609 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890516 | TGAGGTCAAGAGTTC[A/G]AGACCAGCCTGGCCA | 11252 |
| rs757996665 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009863 | ATCATTTTATTTTTT[-/C]TATTTTTTTTTTTTT | 11252 |
| rs758007302 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973247 | AAGGCAGAAGACACT[A/G]TAAAAAGTATTTCCA | 11252 |
| rs758009888 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886376 | ATGGCTGATAAGAAA[C/T]ATGAAAGTACATGTG | 11252 |
| rs758010795 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869365 | TAGAATGGAAATGGG[G/T]AGACTTGCCCATACC | 11252 |
| rs758053517 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933690 | GCCCTCACAGCCCCC[A/G]CACCCTGCACCGTCC | 11252 |
| rs758101074 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872181 | GAGATACAGAGATGA[A/G]AGGAACTGATGGATC | 11252 |
| rs758114517 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895060 | GGTGGTTAGCCTGGG[C/T]AGCCTTCTCCAGAGG | 11252 |
| rs758158634 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009356 | CTTTGGAATGTGCAT[C/T]TTCTATAAATACAAG | 11252 |
| rs758174433 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936842 | CCTGAACCCGCGAGA[C/T]GGAGGTTGCAGTGAG | 11252 |
| rs758180440 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881544 | AGCCTCAGGGGCACC[A/C]GGACCTTTGCCCACT | 11252 |
| rs758211649 | snp | A/C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010715 | GAGACTCCGTCTCAA[A/C/T]AACAACAACAACAAA | 11252 |
| rs758219904 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999920 | GCTCAGAGGCACCGA[C/T]GGCTGTGCTACAATG | 11252 |
| rs758243141 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939837 | ATCCTCTAGTCATTT[A/G]CTTCTTCGCTAATTA | 11252 |
| rs758251295 | in-del | -/AG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955984 | GAATTTAAGAGTCAA[-/AG]AGAGAGAGTTCCAAA | 11252 |
| rs758303218 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914042 | AAGACATTGCCGCTG[A/T]GAGGAGACTGTTGCA | 11252 |
| rs758327899 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985081 | CGCCTGTAATCTCAG[A/C]ACTTTGGGAGGCCAA | 11252 |
| rs758351401 | snp | A/T | 1.6571e-05 | 0.0028784 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912045 | GCTGTCGCTGGACAC[A/T]TCTACTCCAACGGAA | 11252 |
| rs758363389 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994848 | TAGAGCCACAGCCTC[A/G]CAGCCAGCGAATGCA | 11252 |
| rs758389367 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940441 | TACGGATTACACCAG[A/G]TAGCTCTCAAACTTC | 11252 |
| rs758419046 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980143 | CAAGTATAGAGTATT[A/G]GGTGAAAATTTGTAA | 11252 |
| rs758438095 | snp | C/T | 1.65154e-05 | 0.00287358 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884529 | TGTGCCCTGGTCGAG[C/T]TCCTTCAGGGACTTC | 11252 |
| rs758445747 | snp | C/T | 1.65696e-05 | 0.00287828 | missense | PACSIN2 | GRCh38.p7 | 22:42882210 | GCCAGTTCATGGCCA[C/T]GCCCGGCCCGTGATT | 11252 |
| rs758460922 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952943 | AGTGTTGGGATTACA[A/G]GCGTGAACCACCATG | 11252 |
| rs758475486 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875086 | CAATCTCCTGACCTC[A/G]TGATCTGTGTGCCTC | 11252 |
| rs758481080 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882998 | CATGCTGGAGTCCAA[A/T]CCCCAGTGCCTCGGA | 11252 |
| rs758498028 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901099 | TGACCCTGATTTTAA[C/T]CTCAGGATGATCTTC | 11252 |
| rs758515566 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958365 | ACCAAATGAATAACA[C/G]AATTGTGTGGGTGGG | 11252 |
| rs758522422 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930975 | CTCTGAAGAGTGACA[A/G]GCTGGATGCTAAGGG | 11252 |
| rs758537146 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884236 | CCTCCCTGCCATCCA[C/G]ATTACAAAGAAGCAG | 11252 |
| rs758575326 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873353 | GAAACTGGATGAAGA[C/T]GGCTTAAAGGCACAT | 11252 |
| rs758638225 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947594 | AGAGGGGACAACACC[A/G]AAGAACACGCTAGCC | 11252 |
| rs758642365 | in-del | -/G | 1.81628e-05 | 0.00301348 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891204 | GGGGAGAGAAGCTGC[-/G]GGGTCACTCAGCGCC | 11252 |
| rs758666702 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876867 | GCGCGGTGGGAGCAG[A/G]GGAAGCATTTGTTCA | 11252 |
| rs758667984 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959279 | TGTAGATTAGATTTG[G/T]CTGTAAAGAAAGAAA | 11252 |
| rs758683698 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931281 | CAGGGGCACGTTACT[A/T]AACCTTCCTGAACCT | 11252 |
| rs758690877 | snp | C/G/T | 0.000776675 | 0.0196922 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871331 | GCCCGCCGCCTCCGT[C/G/T]CCCCCGCTGGCCTGT | 11252 |
| rs758702217 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919048 | CCATACCTGTGCACA[C/T]GTATGGGACAAGCTG | 11252 |
| rs758741900 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915370 | GGAAGGGACATTCTC[A/C]GGTTACATGGTGGCA | 11252 |
| rs758746617 | snp | A/G | 1.66092e-05 | 0.00288172 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879101 | GTTGATGCCCGTCAG[A/G]GTGACGCCGTCAGTG | 11252 |
| rs758750630 | snp | C/T | 1.65592e-05 | 0.00287738 | missense | PACSIN2 | GRCh38.p7 | 22:42891087 | CGAAGTCATCGTTCA[C/T]CAGTGAGGCCTTCAC | 11252 |
| rs758769216 | snp | A/G | 1.66186e-05 | 0.00288254 | stop-gained | PACSIN2 | GRCh38.p7 | 22:42879148 | TCCGGCTGAGGGTTC[A/G]ATTCAGGTCTGCGGA | 11252 |
| rs758776267 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006770 | CAGTGAGCCGAAATC[A/G]CACCATTGTACTCCA | 11252 |
| rs758793831 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879319 | CCCTGGTTTCCCAGA[A/G]GACCTCAGGCTCCCC | 11252 |
| rs758795323 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976765 | CAGATACCCCATTTC[A/G]TCCTTCCATCAACCC | 11252 |
| rs758832781 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905349 | GAAACGGTAAGTGTA[C/G]AGAGGACGCTCAGAG | 11252 |
| rs758885641 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937411 | CCCAGGCAGGCGGCA[A/G]TAGAAATAACGATGC | 11252 |
| rs758890478 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933199 | GACTTTAAGAAATTG[C/G]AAACAAACTATCTCT | 11252 |
| rs758896922 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954808 | GAATGGGGGATGGGG[C/G]CAGGGATTCAAAGTC | 11252 |
| rs758968234 | snp | A/G | 3.31521e-05 | 0.00407123 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911976 | GGCCTGCCAGACACT[A/G]TTGGCCTGGCCACTT | 11252 |
| rs758973608 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909422 | AAGAGGAACTTGCTA[A/C]CTGCCTGGGAAGATG | 11252 |
| rs758983374 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954067 | GGAGTTCGAAACCAG[A/C]CTAGCCAACATAGTG | 11252 |
| rs758986688 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884505 | CTCCATGTTCTCCAT[A/G]TACTGGGGTGTGCCC | 11252 |
| rs758989555 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965210 | TGTGTCTATGTGGAT[A/G]AAATTCGAAACCAAG | 11252 |
| rs759008935 | snp | A/G | 0.000282207 | 0.0118753 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909520 | ACTCAACGAACATCC[A/G]TCATGGAGAAGGCGG | 11252 |
| rs759048004 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900811 | AGGAAACTGAAGTTT[G/T]AAGAGATGCAGTCAC | 11252 |
| rs759055967 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890815 | TAGCCTGAGGAGTGG[C/T]TTCATCTCTACCAGG | 11252 |
| rs759069024 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926762 | GCTTGAGCCTAGGAG[A/T]TCAAGGCTGCAGTGA | 11252 |
| rs759083779 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006590 | GAGGCAGAGGCAGGC[A/G]GGCCGTTTGAGGTCA | 11252 |
| rs759106829 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890044 | GTCTCCCTCTGTCAC[C/T]AGGCTGGAGTGCAGT | 11252 |
| rs759122907 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910418 | CTGCTGCCAGCTCCA[C/T]AAGCGCTCCTGCACT | 11252 |
| rs759221116 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991003 | TTGTGAGGACTCAAC[C/G]GGTTCTATACACAAA | 11252 |
| rs759222229 | snp | C/T | 1.66821e-05 | 0.00288804 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42879062 | CCTGCTGGGCTTACT[C/T]GGCAGAGACTGGTCG | 11252 |
| rs759225422 | snp | A/C | 1.65924e-05 | 0.00288027 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876847 | GAGGAAGAGAGACAG[A/C]GTGAGCGCGGTGGGA | 11252 |
| rs759283555 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905946 | CTACCTGACCACCCA[C/G]CGCCACCCACTCCTT | 11252 |
| rs759308087 | snp | A/C | 7.37762e-05 | 0.00607311 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871309 | CGTGGCTGGCTGAGG[A/C]TCCTGGGCCCGCCGC | 11252 |
| rs759394281 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985220 | GTAATCCCAGCTACT[A/T]GGGGGCTGAGGCAGA | 11252 |
| rs759409297 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870097 | CACCTGCTCCCGGGC[A/G]ACTCCGGGCAGCCCG | 11252 |
| rs759434680 | snp | G/T | 1.66043e-05 | 0.00288129 | missense | PACSIN2 | GRCh38.p7 | 22:42879120 | ACGCCGTCAGTGGCC[G/T]TCTTCTTCTCTCTCC | 11252 |
| rs759449392 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892140 | GTCCCCGAGGCTCAG[A/G]AAGGAAGCCCTAATC | 11252 |
| rs759462141 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002935 | CAATTATAACAATGT[C/G]AGTTATTGAAAAGGA | 11252 |
| rs759464060 | in-del | -/CTG | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896414 | GTTCACTCTTTCTTA[-/CTG]CTAAGTAGTATTCGA | 11252 |
| rs759488672 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006380 | CCTAGTGATGGAGCT[C/T]GAACCCACACCCAAG | 11252 |
| rs759532303 | in-del | -/AAAAAAAAAAAAAAAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982888 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAC]AACAACAACAAGGCT | 11252 |
| rs759569346 | snp | A/G | 1.69841e-05 | 0.00291407 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893638 | AGAACCAGCTGGGAG[A/G]CAGGGGGCTTGGGGC | 11252 |
| rs759580382 | snp | A/G | 3.3134e-05 | 0.00407012 | missense | PACSIN2 | GRCh38.p7 | 22:42876211 | CGCACTTCCGTCCCC[A/G]AGGTGGCGTCGTCGT | 11252 |
| rs759621987 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001413 | ACCAGAGCAAAGTAC[A/G]ATTTCCACACTTGTG | 11252 |
| rs759633284 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013635 | CCTGGGCTCCAACCT[A/G]GCAATCCCAGGAGGG | 11252 |
| rs759643472 | in-del | -/CATACATACATG/CATC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012157 | CAAAATAAATAAATA[-/CATACATACATG/CATC]CATACATACATACAT | 11252 |
| rs759676925 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912764 | CATAAGCACAAACCA[C/T]ACCTTGCTAGTGTGA | 11252 |
| rs759726904 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933996 | GTGAAAAGCTACAAT[A/G]ACTCACACTGTTCTC | 11252 |
| rs759729412 | snp | C/T | 1.65754e-05 | 0.00287879 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912056 | ACACTTCTACTCCAA[C/T]GGAATCATCATATGT | 11252 |
| rs759762343 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992942 | GCTGAGGCGGGCAGA[C/T]TGCCCGAGCTCAGGA | 11252 |
| rs759788319 | snp | A/C | 1.6566e-05 | 0.00287797 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888821 | GAGAATGAGTTCCTG[A/C]ATGCCATGTCACTGG | 11252 |
| rs759801069 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960255 | CTGCATCTGAGGGGC[A/G]TCACAGCAGTCAGTG | 11252 |
| rs759820703 | snp | A/G | 1.66615e-05 | 0.00288626 | missense, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893532 | TCTCGATGCGCGCCC[A/G]CTCATGCAGGCAGTT | 11252 |
| rs759820735 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956637 | TAGTCTTAGAGAAGG[C/T]TCTGAGGCCACTTCT | 11252 |
| rs759823882 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964731 | GGGACGACAAAGTTA[G/T]ACAAAAGACCAAAAG | 11252 |
| rs759846474 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929571 | TATCTCAGAACTCCA[A/G]AACGATCCTGTCTGG | 11252 |
| rs759852739 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922476 | AGCCCCCGATACCCC[A/G]CTCTAATCCTCTAAC | 11252 |
| rs759870135 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999446 | AGGCCAAGGCCAGTG[A/G]ATCACCTGAGGTTGG | 11252 |
| rs759909873 | snp | C/T | 1.65822e-05 | 0.00287938 | missense | PACSIN2 | GRCh38.p7 | 22:42882240 | TGGCTCGGAACCACC[C/T]CAGGTCCTCCACTGC | 11252 |
| rs759915415 | in-del | -/AAAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980080 | TGTTAATTAAAAAAA[-/AAAG]AAAGAAAGAAACAAT | 11252 |
| rs759918293 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881809 | GGCCCACCGTGAGGG[A/G]AGCACTGTGGCTGCT | 11252 |
| rs759951962 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939277 | GTTGGCAAGCACCCT[C/G]GGAATGTGGAGATGG | 11252 |
| rs759963695 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008835 | ATTTTTACTTAACAT[A/T]TATTTCACAACTTTC | 11252 |
| rs759971262 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893390 | AGAGAGGGTCACAAC[A/G]TGCCCAGAGCCCCCG | 11252 |
| rs759995373 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978583 | CACCCACACAGAGCA[A/G]AAAGCAGGAAGGTTT | 11252 |
| rs759996281 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949712 | ACACACACTCTCTCA[-/CA]CACACACACACACAG | 11252 |
| rs759997670 | snp | C/T | 5.00455e-05 | 0.00500202 | missense | PACSIN2 | GRCh38.p7 | 22:42876142 | GCCCACCTACCAGCC[C/T]TGAAGCTCAGCTCAT | 11252 |
| rs760014272 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956340 | AATAAGAAAAAACTT[A/T]GGCCAGAGCCCCAGG | 11252 |
| rs760048795 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979628 | GAAGTAATTGGCCCA[C/G]GTCAGATACCTCCTT | 11252 |
| rs760055830 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903012 | CAGTAACTTCATGGC[C/T]GGCAGAAGAGCAACT | 11252 |
| rs760064191 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008018 | CTGCAACTCTATCAA[C/T]AGTCACATCACACAT | 11252 |
| rs760079341 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928981 | CTCTTAGAGTTCTCT[A/G]AGTTTAAAATGTTTT | 11252 |
| rs760079345 | in-del | -/CACT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945275 | TGGGGAGGGAGCTGA[-/CACT]CACCAGCTCATTTCT | 11252 |
| rs760083886 | in-del | -/AG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014327 | CCCCGCCCTACACAC[-/AG]ACACACACACACACA | 11252 |
| rs760115512 | snp | A/G | 9.93443e-05 | 0.00704715 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876930 | CTGACGGTGCTGCCC[A/G]TGTCGTCCTCATCCT | 11252 |
| rs760125021 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978688 | TGCTTTTTGGCCTGC[A/G]GACGTTCAGGTGGAC | 11252 |
| rs760130756 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940300 | TAGAAGGAAAGAAAT[A/G]TAGTGCAGAGTGAGT | 11252 |
| rs760173151 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007655 | GTAGTGTCCTGAGGA[C/T]AGTCAGACCCGCCCT | 11252 |
| rs760181011 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876804 | TGCATTGCCGAGTGC[C/T]GAGGGGTGAGACCCC | 11252 |
| rs760199673 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892171 | CAGGCTGGCATTTCT[A/G]TTCAGGGGGTAGGGT | 11252 |
| rs760200541 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880670 | CATTAGAGAAAGGCA[G/T]GGTCCCGTAACAGCT | 11252 |
| rs760209745 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965075 | TGTGTGTGGCATCGG[C/T]GCACAGCTGAAAACC | 11252 |
| rs760226745 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998330 | ACCTGGTTTGGATTC[C/T]GGGCTCCCAACCTTG | 11252 |
| rs760291346 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927842 | TCCGCCTGCCTCAGC[A/C]TCCCAAAGTGCTACA | 11252 |
| rs760305036 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916605 | CTCCCCGCTCTCACC[C/T]TGACAAGCCTCCCTT | 11252 |
| rs760338311 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944748 | TTCCATCCGAAATTG[G/T]GTATAAGCAAAAAAG | 11252 |
| rs760356807 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886150 | CCCTCAGCCTGTGCC[A/G]ACCCTGCTAGCCCCA | 11252 |
| rs760393587 | snp | C/G | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871859 | CTCCCCAGGGCCCCG[C/G]CCGCCTTGCTCCCAG | 11252 |
| rs760421212 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938868 | GAGAAGGTAAAAATG[C/T]TGTCTGTGACAAATT | 11252 |
| rs760468172 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969197 | TCCATTCTCAGTTTG[A/C]AATATGGAGATAATT | 11252 |
| rs760473068 | in-del | -/CAA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996531 | AGCAAGACTCTGCCG[-/CAA]AAAAAAAAAAAAAAA | 11252 |
| rs760511481 | snp | A/G | 1.65952e-05 | 0.00288051 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882138 | AACTCTGTGGGCCCA[A/G]GTCCTCTTCCAGGCT | 11252 |
| rs760514246 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956072 | TTTCCAGCAAAATCA[C/T]TCTTCCTTGTTCTCC | 11252 |
| rs760538715 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972955 | AAATAAAAGCACACA[C/T]CTGGATTTTCTAATT | 11252 |
| rs760544361 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013762 | TCAAACTCTTTGAGC[C/T]GGTTTCCTGATTTTC | 11252 |
| rs760555896 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004003 | ACAGACATAGATGCC[A/G]TCTTAAGCAAAGGAC | 11252 |
| rs760559551 | in-del | -/ACACACACAT/ACACACACATAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889375 | TTTAATGGTTTTTAC[-/ACACACACAT/ACACACACATAG]ACACACACACACACA | 11252 |
| rs760567088 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945802 | GCAGCCACTTGTTTA[A/G]TCCCCGACTCCCTTC | 11252 |
| rs760567589 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967611 | CCCTGCAAATGGGCC[A/G]GGCGCGGTGGCTCAC | 11252 |
| rs760582475 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973567 | TTGGAATTTACACAT[C/T]TGATAGCTGCAAAGC | 11252 |
| rs760625986 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907024 | CCCGGAGCAGTCAGG[A/G]AAGGCTCTTCCTTTC | 11252 |
| rs760645842 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944713 | CACATCCGTTACAGA[A/G]AACTAGCAGGTGAGC | 11252 |
| rs760651671 | snp | A/T | 1.65974e-05 | 0.0028807 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912085 | GTGACAGACATTTTT[A/T]CAAAGGCTGAGGGAG | 11252 |
| rs760655190 | snp | C/G | 2.50919e-05 | 0.00354194 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890893 | GAGGTGGTGCTGCTA[C/G]TGGGGTGCCAGGCAG | 11252 |
| rs760673497 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940016 | ACCAGACACAATTAC[C/T]GGGTTTCTAAAATGG | 11252 |
| rs760695235 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008930 | AGTCTGCTCAAAACA[C/T]TCAAGCCCTACAAAC | 11252 |
| rs760758276 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004611 | TGATCTTGGCACGCT[C/T]GGTTGGCGACAACAT | 11252 |
| rs760790751 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885523 | TGAGGAAGGATGGAG[C/T]GCTTCCCGAGACACT | 11252 |
| rs760811420 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994442 | CCTCGGGCGTGCTTA[C/T]GGGGACACCCCAGCC | 11252 |
| rs760841087 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903072 | GTCACATAAGCACAG[C/T]CAGCTGCAGGGCCTC | 11252 |
| rs760894481 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912873 | GTTCAGATCACACAG[C/T]CAGAGATCCAAGACC | 11252 |
| rs760898457 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993680 | TGATAACACGATTGC[A/C]GACTGTCATCTTCTG | 11252 |
| rs760943770 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925347 | TAGCTGTGTGTGGTG[A/G]CGCATGCCTGTAGTT | 11252 |
| rs760958763 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920934 | CGGCCTCCCCAGTAG[C/T]TAGAACCACAGGCAT | 11252 |
| rs760960593 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978016 | GAAAAAGACTAGAGC[A/G]ATTCAGTGTGACATA | 11252 |
| rs760960785 | snp | C/G | 1.6571e-05 | 0.0028784 | missense | PACSIN2 | GRCh38.p7 | 22:42884409 | ATTGGACAGGTCTAG[C/G]TGCTTCTGAACCTCC | 11252 |
| rs760986779 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976096 | ACATTCATCATCTTA[C/T]TTTGCATGTAGGAGA | 11252 |
| rs761058924 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873148 | AGCTTTCACATTGTG[C/T]AAATGTGAACTGGTG | 11252 |
| rs761081814 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929732 | AGTGACCCGCCACCC[A/G]GGGCTCCAAACAGAG | 11252 |
| rs761091871 | snp | A/G | 1.71619e-05 | 0.00292928 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884359 | TGACTTCAATGACGT[A/G]TGTGTTTTAGCTCAA | 11252 |
| rs761094569 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896030 | TCTAGGTCGAGATGG[A/G]ATCTACACACAGGCA | 11252 |
| rs761114005 | snp | G/T | 1.65658e-05 | 0.00287795 | missense | PACSIN2 | GRCh38.p7 | 22:42876220 | GTCCCCGAGGTGGCG[G/T]CGTCGTCGAATGGAT | 11252 |
| rs761135723 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882506 | CTGACAAATGAGCTT[C/T]AAATCAAACCAGCCA | 11252 |
| rs761137403 | snp | A/C | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896073 | ACAGGGTACACTTAG[A/C]TCTGAATGTGGACAA | 11252 |
| rs761137933 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968601 | AAAGCCTGATTTTGG[G/T]GTGTGTCCATGGGGC | 11252 |
| rs761162806 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010006 | TCCCGAGTAGCTGAG[A/G]TTATAGGCGCACGCC | 11252 |
| rs761166454 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989918 | TATGTATATATATGT[C/G]TGTATATATAGGTAA | 11252 |
| rs761168062 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001373 | AAGGCAACAGCAACC[C/T]AGACATGTTTAGGCA | 11252 |
| rs761181351 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009994 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGATTA | 11252 |
| rs761189042 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969518 | ATTTAAGATGAGTAA[C/T]CCTCCCACCTCAATA | 11252 |
| rs761238815 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941390 | GACAGATGTTTTCAT[G/T]TCTTTTGAGTAGATA | 11252 |
| rs761279029 | snp | A/G | 1.65696e-05 | 0.00287828 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877016 | ATTAAGGGTGCTATG[A/G]AGAGAGAGAGCTTTC | 11252 |
| rs761319156 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917669 | TGCTCTGCGGTGTGC[C/T]GTGATGAACTACTGC | 11252 |
| rs761322300 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881663 | GATAATGAAAGCTTA[C/G]ACCCACATGATGGGA | 11252 |
| rs761325058 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998577 | GAAACTCCAGATGAC[A/C]AAAGGCTACTGTAAA | 11252 |
| rs761331760 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894663 | TAGTTCATCAAAGTT[A/G]TAAGTAATAAAAGAG | 11252 |
| rs761340140 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010687 | AGGGCACTTCCAGCC[C/T]GGGCAACAAAGCGAG | 11252 |
| rs761348165 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957071 | CGAACTAAGCCACTG[C/T]GGCTCCTGAGCCTGC | 11252 |
| rs761371956 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928801 | TAATTTCATTTTTGA[C/T]AATTCTGAAGTCATT | 11252 |
| rs761408594 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013825 | TGTACCAAGTAGCCC[C/T]GGAGACTCTGAGCAG | 11252 |
| rs761414845 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935218 | GCGTGAGCCACCGTG[-/C]CCAGCCCAGGGCATG | 11252 |
| rs761423001 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918372 | ACCTGGGAGCCCAAG[A/C]TACAAATTTTCTAGA | 11252 |
| rs761434727 | snp | A/G | 1.70638e-05 | 0.00292089 | missense | PACSIN2 | GRCh38.p7 | 22:42893465 | CCCATACCTTTCTCC[A/G]CGAGCTGCCTCCAGC | 11252 |
| rs761464603 | in-del | -/AAAAAAAAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919773 | GCAAGAACCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 11252 |
| rs761485943 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008649 | AAAATGTTAGGAATC[C/T]AGCCAGAAGGCCACA | 11252 |
| rs761494553 | snp | C/T | 1.69568e-05 | 0.00291172 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876108 | GGTTGGAAGCCCTCC[C/T]CCCCTGGATGCTGGG | 11252 |
| rs761518291 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880677 | GAAAGGCATGGTCCC[G/T]TAACAGCTGCAAATG | 11252 |
| rs761522381 | in-del | -/AGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975390 | TTGGGAGGCTGAGGC[-/AGG]AGAATTGCTCGAGCT | 11252 |
| rs761552870 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925587 | CAAAGCAGTTGCTTT[A/G]TAAATTGCTGGATGA | 11252 |
| rs761566930 | in-del | -/CAC | 1.67036e-05 | 0.0028899 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871509 | CCATGAGAGGTATGA[-/CAC]CACCGACGGTGGGCT | 11252 |
| rs761587303 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956198 | GCCATACTATTGTGA[C/T]GACCACTGGCACACA | 11252 |
| rs761587879 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913765 | TTTGCCCACGGTTGT[C/G]CAAGTAATGGCTGGT | 11252 |
| rs761600120 | snp | C/T | 0.000132959 | 0.00815241 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888602 | CACGTCAACAACTGA[C/T]ACGGTGACACTCGAC | 11252 |
| rs761603768 | snp | A/G | 1.66286e-05 | 0.0028834 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893554 | CAGGCAGTTCATGAG[A/G]TCGCTGCACAGGCGG | 11252 |
| rs761604011 | in-del | -/CTGA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942881 | CTTTTCAAAACTGTT[-/CTGA]CTATTCTTGGTCCCT | 11252 |
| rs761605978 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926515 | AACAGTGGGAGGAAG[A/G]GGAATCTTAGGAACT | 11252 |
| rs761635264 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888442 | CTGGCTCTGTCCCTT[C/G]ACTGAGCAGGTACAG | 11252 |
| rs761685863 | snp | A/G | 4.96742e-05 | 0.00498344 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876947 | GTCGTCCTCATCCTC[A/G]AAGGGGTTGTAGCTG | 11252 |
| rs761689851 | snp | C/G | 1.65597e-05 | 0.00287743 | missense | PACSIN2 | GRCh38.p7 | 22:42888701 | TTCTTGAGCTGTTCA[C/G]GGTTGAGGGATGGGT | 11252 |
| rs761693452 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886114 | GTGGCAACAAGATGC[A/T]CCACCTCTGGGCTGC | 11252 |
| rs761695647 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004771 | CTATCTAAAGACCAC[C/T]CTGCAGGTCCAGGCA | 11252 |
| rs761697107 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990867 | AAAAATGCTAAACCA[C/T]ATCTGTCCTTCAATG | 11252 |
| rs761710414 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973725 | TGACACAGAAACAGG[C/T]CTGCTACACTCCAGT | 11252 |
| rs761715342 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932466 | AGCGTATCTCACATA[G/T]GACAACAGGTCCTTT | 11252 |
| rs761726100 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888464 | CAGGTACAGTGGCTA[C/T]GGTGAGGCGAGGTGC | 11252 |
| rs761750696 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005361 | AATTACCAACCCAGA[A/G]GAGAGCAAGGCCTCT | 11252 |
| rs761752453 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869778 | GACTTCCATATGCAC[A/G]AGATCAACTGTTTAT | 11252 |
| rs761775263 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899523 | CCTGTGGACTGGCAA[A/C]CACCAGAGAGTGGGA | 11252 |
| rs761783687 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004230 | AGCTTAGGTTTACTG[A/G]TGGATCAAGTGGAGA | 11252 |
| rs761791174 | snp | C/G | 1.66084e-05 | 0.00288165 | missense | PACSIN2 | GRCh38.p7 | 22:42879138 | TTCTTCTCTCTCCGG[C/G]TGAGGGTTCGATTCA | 11252 |
| rs761810536 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892983 | TCGGTGGGGACAGAA[-/G]GGGGTGAAACCTCTG | 11252 |
| rs761825863 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880755 | AGAGAGAAGGACCCC[C/T]TAGGCTCTGGCTGGG | 11252 |
| rs761827804 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904679 | AAGCCTCCCCACCTC[C/T]TTCCGTTCCCTCCTC | 11252 |
| rs761837978 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000637 | ACTTTAAGGAAGGTG[A/G]CTTGTCTGAGCTATA | 11252 |
| rs761904578 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905391 | TCGGGAGTCATTTAG[A/T]CTTGGCCTTGCCATG | 11252 |
| rs761931057 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011575 | TAAGCCTGAGCATGA[C/T]GCCCTTAACACAGCA | 11252 |
| rs761934600 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942907 | TGGTCCCTTGCATTT[C/T]CACAGGGATTTTAGA | 11252 |
| rs761947967 | snp | C/T | 1.67072e-05 | 0.00289021 | missense | PACSIN2 | GRCh38.p7 | 22:42891161 | GCCATCCAGGCCTTC[C/T]CCACGGTCCCGTACT | 11252 |
| rs761956899 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984258 | ATTACAGGTGTGAGC[C/T]ACCACCCACTACCTA | 11252 |
| rs761985989 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931947 | AACTCAACGTTAAAG[A/T]GAACAGAAAACCTAT | 11252 |
| rs761996112 | in-del | -/GAGA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960588 | AAAGCTTTAGGTGAG[-/GAGA]GAAAGATTTTAAAAT | 11252 |
| rs762058366 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979923 | TTGTAAATTTACATA[C/T]ACACATTTATTACAC | 11252 |
| rs762067155 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911634 | ATGTCAAATCACAGC[C/G]CTCCTTGTTTCTACA | 11252 |
| rs762080799 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953182 | TAAAATGTTTTCTAT[C/T]CTTCCATTGTTCAAG | 11252 |
| rs762082441 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925040 | TGAGCCACTGCGTCC[C/G]GCCCCAGTGAGAACT | 11252 |
| rs762083816 | snp | C/T | 3.32696e-05 | 0.00407844 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871490 | AGACAAAGAGGGAGC[C/T]GTCTCCATGAGAGGT | 11252 |
| rs762103592 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948820 | TATGGAGCCAGTTTC[A/G]TGTGACAAACTGATA | 11252 |
| rs762135818 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984480 | AACACTGGTCCCATC[A/T]TGCATCTCCCCAGAC | 11252 |
| rs762165821 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941736 | CATTTTTTAAACTGG[C/T]GTGTCTTCTTATTGC | 11252 |
| rs762179110 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972508 | AATCATCAATAAATA[C/G]TAAATATATATATAT | 11252 |
| rs762192138 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955471 | CCTGGAGATAGCATC[-/A]GGGGGAAAAAAAAAA | 11252 |
| rs762205164 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915549 | ACAGCTCAATCTGTA[A/G]TAACATCAGCTCAAC | 11252 |
| rs762230936 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875834 | GAGCCACCATGCCTG[G/T]CCTAATTTTTTGTAT | 11252 |
| rs762239205 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884490 | CTGCTCAAACACCTG[C/T]TCCATGTTCTCCATG | 11252 |
| rs762245511 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939911 | AGCGTGCAAGATAAA[G/T]TCCCTGACTTCTAGA | 11252 |
| rs762256300 | in-del | -/TATTTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009863 | TCATTTTATTTTTTC[-/TATTTTTT]TATTTTTTTTTTTTT | 11252 |
| rs762275619 | snp | A/G | 8.27959e-05 | 0.00643359 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891073 | GTTCTTGATCTTCTC[A/G]AAGTCATCGTTCATC | 11252 |
| rs762280315 | snp | A/C/G | 3.29669e-05 | 0.00405984 | missense, synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884472 | CTCCTCGAACTGCTG[A/C/G]CACTGCTCAAACACC | 11252 |
| rs762295839 | in-del | -/AGAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974998 | ACTGTGCCAGGGCCT[-/AGAA]TGTGGGTCAGGGAGA | 11252 |
| rs762323144 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976631 | AGAATTGTATTACAT[A/G]CCTTTTAAATATGCT | 11252 |
| rs762331945 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001568 | CAGACGAGCCCTGAA[A/G]TGTGGGCACAAAAAC | 11252 |
| rs762334519 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948040 | GGGGACACATAGAGG[C/G]TCCAGAAAGGGTGCC | 11252 |
| rs762336434 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960095 | AGGGAGAAGAGGTCT[A/G]AGAACAAAATTCATA | 11252 |
| rs762362559 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970376 | CTGGATGGGATCCTA[C/G]AACTGCAAGAAAACA | 11252 |
| rs762373695 | snp | C/T | 1.69367e-05 | 0.00290999 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893632 | GGAGAGAGAACCAGC[C/T]GGGAGGCAGGGGGCT | 11252 |
| rs762384894 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991294 | TCAAGGACAAGCAGT[A/G]GCTCAGAGCAGAGCC | 11252 |
| rs762416604 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016556 | GGGAGTCTGAGGCAG[A/G]AGAATCACTTGAACC | 11252 |
| rs762436292 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921106 | GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA | 11252 |
| rs762455264 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915244 | TTTAGGAGTAAGAGC[C/G]TGAATCACTGAGGAG | 11252 |
| rs762455370 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907952 | AAACCAGCCCGACTC[A/T]GAGCAAGTTGCAACA | 11252 |
| rs762492450 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957219 | CACTGCATAAAAATA[C/T]TGCTTATGTATTCCA | 11252 |
| rs762507237 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948215 | GCTGTGGCTGTGAAG[A/G]AGGGGAGAGGGGACT | 11252 |
| rs762517944 | snp | A/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015755 | CACCTTGCATGATAG[A/G]GTATTAGCCCCGTTC | 11252 |
| rs762537875 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920135 | AAAATTAAAAATAAG[-/A]AAAGAATCTAAAAAA | 11252 |
| rs762537972 | snp | A/G | 4.9894e-05 | 0.00499445 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893568 | GGTCGCTGCACAGGC[A/G]GTGGCCATCGTCGAT | 11252 |
| rs762566627 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004809 | CGTCACAGGCCTCCC[C/T]GGGCGCTCTGGGCTT | 11252 |
| rs762573548 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882411 | TCTGCCCTCTGTGAG[G/T]TGGTTTCACAGACAG | 11252 |
| rs762647626 | snp | A/G | 1.6534e-05 | 0.00287519 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884426 | GCTTCTGAACCTCCA[A/G]CAGAACCTCCCGGAA | 11252 |
| rs762657989 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000257 | ACCCCAAAAGCCAGC[C/G]ATCCTGGACAGCAGG | 11252 |
| rs762670462 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954320 | GTGGAGAACAGCCCA[C/T]TGAGCCTCTAGTCTT | 11252 |
| rs762694229 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914945 | CACAGCTCACTGCAG[C/G]CTCGAACTCATGGGC | 11252 |
| rs762727209 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947265 | GAATGCTCCAGGCCA[C/T]CTTCGAGGTCTGCTG | 11252 |
| rs762753372 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005411 | TCAAAACCCAGGGAG[C/G]ATATGACCATCATCA | 11252 |
| rs762792762 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879845 | TCTCAGTCTCCAAAG[C/T]GCAGGGCCCTCCCCA | 11252 |
| rs762795587 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915908 | AGCCCTAAGGCGACA[C/T]TGAGGCAAGATATAG | 11252 |
| rs762820834 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888802 | TGCTGCTTCTACCTA[C/T]AGGGAGAATGAGTTC | 11252 |
| rs762847729 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010492 | AGGCGGGCAGATCAC[C/G]AAGGTCAGGAGATCA | 11252 |
| rs762854766 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963752 | GTCCCTCCTCTCTCT[A/G]CCACACCCGTGCCTC | 11252 |
| rs762901632 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996956 | CAAAATGAGCCTCAA[C/T]AAACATTAAATTTTT | 11252 |
| rs762906972 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884596 | CAAGACAGAGGTTCA[C/T]TTCCATTTAGCCCTT | 11252 |
| rs762947383 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925883 | TGGGTCCCTGGGCCC[C/T]CTATGTCACCAGCCT | 11252 |
| rs762964253 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901672 | CTCTCCGCCTGCCAC[A/G]GCGATCGCCTGACAA | 11252 |
| rs762980563 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936859 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCATAG | 11252 |
| rs762989874 | snp | C/T | 1.6577e-05 | 0.00287893 | missense | PACSIN2 | GRCh38.p7 | 22:42882230 | GGCCCGTGATTGGCT[C/T]GGAACCACCTCAGGT | 11252 |
| rs762992837 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995958 | GGGCGTGGTGGCTCA[C/T]GTCTGTAATCCCAGC | 11252 |
| rs762993420 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991632 | AGGAGCTGGGAACTC[C/G]CAGGTGCGATAAAGA | 11252 |
| rs763016581 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001707 | TCAGCTTTTCTTAGC[C/T]GGGATAAGAGGAACC | 11252 |
| rs763019917 | snp | C/T | 1.65677e-05 | 0.00287812 | missense | PACSIN2 | GRCh38.p7 | 22:42876209 | CTCGCACTTCCGTCC[C/T]CGAGGTGGCGTCGTC | 11252 |
| rs763038061 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927925 | ACGTCATGTCATGGT[-/C]CCCATACTCCACTGA | 11252 |
| rs763048043 | snp | A/G | | | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888763 | CAGCTTCTCCTCTTT[A/G]CACGCTGCATGGTGG | 11252 |
| rs763058537 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911408 | GAGACCTCAACTGTT[-/A]AAAAAAAAAAAAAAA | 11252 |
| rs763071549 | snp | A/T | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002415 | AGTAAGGATTTTCTA[A/T]AACAGCGTTCCTTGC | 11252 |
| rs763079262 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870729 | TCCCAATAGAAACCC[A/G]ACCATAACCCGGTCC | 11252 |
| rs763089240 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979267 | GGTGGCTCATGCCTG[A/C]AATCTCAGCACTTTG | 11252 |
| rs763091611 | snp | C/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896430 | TGCTAAGTAGTATTC[C/G]ACTGTGTAGGTATAC | 11252 |
| rs763094591 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011647 | TCTGCGAGGCCGAGG[C/T]GGGCAGATCACTGGA | 11252 |
| rs763108619 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947949 | CACTCCATTCTCACA[-/G]GGTCGATGGACACTT | 11252 |
| rs763153760 | snp | C/G | 1.68795e-05 | 0.00290507 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876119 | CTCCTCCCCTGGATG[C/G]TGGGGGAGCCCACCT | 11252 |
| rs763204262 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902899 | GAATACAGGTGTGAG[A/C]CACCGCGCCCGGCCT | 11252 |
| rs763216233 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920995 | GAGACGGGGTTTCGT[C/T]GTATTGCCCAAGCTG | 11252 |
| rs763220396 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944604 | TAGCTTGGACAAAAT[-/G]TTCATCACTGCAATA | 11252 |
| rs763225418 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942983 | GTAGCTCAATTTGAG[A/G]AGTACTGCCATCTGA | 11252 |
| rs763248895 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939079 | CAGGCCCCAAGGTCA[C/T]CCGTCCCAGCGCAGC | 11252 |
| rs763267165 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007915 | CATGAGCCACTGAGA[C/T]ATCCTCCAAACACTC | 11252 |
| rs763277842 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892227 | GAGAGCCACAACGGA[A/G]CCGGGGCAGAAATCG | 11252 |
| rs763282738 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869963 | CTGCTCACTGGAAAC[A/G]GAGTGAATGCATAGC | 11252 |
| rs763296353 | in-del | -/ATA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989882 | AATATATATATATAT[-/ATA]TACACACACACACAC | 11252 |
| rs763314017 | snp | A/G | 1.67666e-05 | 0.00289534 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891166 | CCAGGCCTTCTCCAC[A/G]GTCCCGTACTGGGGC | 11252 |
| rs763317556 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004318 | CCCTCAGAAACTTCA[C/G]AACATGGGGGCCTGT | 11252 |
| rs763359549 | in-del | -/ACTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880611 | TAGCCGAACGCAGAC[-/ACTT]ACTTCATCCTTGTGG | 11252 |
| rs763380092 | in-del | -/ATG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008195 | AAAAACATCTTTATT[-/ATG]ATTATTTTCATCAGA | 11252 |
| rs763403210 | snp | C/T | 1.72472e-05 | 0.00293654 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893432 | GCTGCCTCCAGGCCA[C/T]AGGACCTGTGCCGGG | 11252 |
| rs763431507 | in-del | -/AATA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997568 | CTCAAAAAAAAAAAC[-/AATA]AATAATAAATAAATA | 11252 |
| rs763479678 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966109 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11252 |
| rs763489106 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938384 | TGATGCAGAAACTGC[A/G]TAAGGAATCCTCCCC | 11252 |
| rs763494448 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960825 | GTACACTTGAGATCT[C/G]TGCACTTTAGGTATG | 11252 |
| rs763509359 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870982 | GATGTAAGCTTGTTC[A/G]TTTAAGTTGCAGGTG | 11252 |
| rs763544195 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872374 | TTGGGCCTGCTGGCT[C/T]GGACCTCGTCAGGAG | 11252 |
| rs763547723 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924760 | GTGAGGTTTTTTTTC[-/T]TTTTTTTTTTTTTCG | 11252 |
| rs763558242 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944716 | ATCCGTTACAGAGAA[C/G]TAGCAGGTGAGCTAT | 11252 |
| rs763560316 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880675 | GAGAAAGGCATGGTC[C/G]CGTAACAGCTGCAAA | 11252 |
| rs763562654 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998356 | CCTTGCTTCCAGTTT[A/G]TAACTCAACCCAGCC | 11252 |
| rs763576345 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885522 | CTGAGGAAGGATGGA[A/G]CGCTTCCCGAGACAC | 11252 |
| rs763592372 | snp | C/T | 6.62306e-05 | 0.00575421 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876934 | CGGTGCTGCCCGTGT[C/T]GTCCTCATCCTCGAA | 11252 |
| rs763613568 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986281 | CCACTGCGTCAGCCA[C/T]GACGCTGGGCTGCAG | 11252 |
| rs763638065 | in-del | -/ATATAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989882 | AATATATATATATAT[-/ATATAC]ACACACACACACATA | 11252 |
| rs763714780 | snp | A/C | 1.71599e-05 | 0.0029291 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893449 | GGACCTGTGCCGGGG[A/C]CCCATACCTTTCTCC | 11252 |
| rs763762078 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879997 | CAACCGCACTGAAAA[G/T]GGACTAGGGCAAAAC | 11252 |
| rs763775543 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974749 | GTGAGATCTTGTCTC[-/A]AAAAAAAAAAAAAAA | 11252 |
| rs763776178 | snp | A/G | 1.70284e-05 | 0.00291786 | missense | PACSIN2 | GRCh38.p7 | 22:42891179 | ACGGTCCCGTACTGG[A/G]GCCCTGTGCAGGGGA | 11252 |
| rs763782759 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969971 | CGTTTCAACAAGTAT[C/T]AACACATGGCCAATC | 11252 |
| rs763833026 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909131 | AGCATCCAAGTGCAG[-/C]CAACGTCCACTACCC | 11252 |
| rs763921084 | snp | A/T | 1.66316e-05 | 0.00288367 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871487 | GCAAGACAAAGAGGG[A/T]GCCGTCTCCATGAGA | 11252 |
| rs763939558 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004121 | TCACAACTTACTTAT[C/T]CCAGCCAGCCAGAGG | 11252 |
| rs763940841 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961144 | GGCAAAAGAACATAC[A/T]GCAAGGGGAAACTGT | 11252 |
| rs763941275 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907981 | CAACCTACAGGGAGC[A/G]CCTTCCTGGCAGGGA | 11252 |
| rs763952221 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897811 | CAGGTAGGAGGCTGG[A/C]CAGATTAAAGGTGAG | 11252 |
| rs763985490 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | PACSIN2 | GRCh38.p7 | 22:42884515 | TCCATGTACTGGGGT[A/G]TGCCCTGGTCGAGTT | 11252 |
| rs763993291 | snp | C/T | 9.95487e-05 | 0.00705439 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876853 | GAGAGACAGAGTGAG[C/T]GCGGTGGGAGCAGAG | 11252 |
| rs764000007 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886236 | TCCCCTTGCAGGGCA[C/T]AGAAAGTTCTCAGCG | 11252 |
| rs764019923 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960677 | AAGGCGTAACTAATC[C/T]ACACCCTTCGAAGCC | 11252 |
| rs764022480 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973003 | ATTGTTCATTGTGAA[A/C]CAGATTTATCATGAC | 11252 |
| rs764036156 | snp | A/T | 1.65603e-05 | 0.00287747 | missense | PACSIN2 | GRCh38.p7 | 22:42891047 | TGCTTGTGAAAGGCT[A/T]CCTTCTGCCAGTTCT | 11252 |
| rs764045473 | in-del | -/A | 1.67621e-05 | 0.00289495 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871335 | CCGCCTCCGTCCCCC[-/A]CGCTGGCCTGTCCCC | 11252 |
| rs764073180 | snp | A/C | 1.71161e-05 | 0.00292536 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884608 | TCATTTCCATTTAGC[A/C]CTTGGCTCACCCTGC | 11252 |
| rs764094462 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989027 | TGGGACCACAGGCAC[A/G]TACCATGACACCTGG | 11252 |
| rs764117256 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013010 | TTAGCCAGGCTGGTC[G/T]CTAAGTTCTGACCTC | 11252 |
| rs764138439 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002960 | AAAGGAAACAGCGAG[A/G]TCAGTTCAAGCTCCA | 11252 |
| rs764143814 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907040 | AAGGCTCTTCCTTTC[C/T]CAGAGCAGCTCCCTA | 11252 |
| rs764168509 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013790 | TTCATCAAGACAGCC[A/G]GGCAGTATTTGGTAA | 11252 |
| rs764172242 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906413 | GTGTATTCTAAACTG[C/T]GAAAACCACCCATTT | 11252 |
| rs764209575 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979859 | TGTTGCCCAGTGTGC[C/T]GAAACACGTTTGTCT | 11252 |
| rs764247275 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912936 | TTAGCTTAGCAACAG[G/T]AAGGGGTGAGACAGA | 11252 |
| rs764251868 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877936 | AAGGGAGGCGAGGAC[A/G]TGCCTCCAATGCCAC | 11252 |
| rs764252398 | in-del | -/AGTA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886450 | GTAGGTAGGTAGGTA[-/AGTA]GGTATGTATGTACCT | 11252 |
| rs764270378 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972513 | CAATAAATACTAAAT[-/AT]ATATATATATATATT | 11252 |
| rs764285999 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978871 | CTTTGGGAAATCTCC[A/C]TACTCCTTCAAAACA | 11252 |
| rs764294309 | snp | C/T | 4.96964e-05 | 0.00498455 | missense | PACSIN2 | GRCh38.p7 | 22:42876221 | TCCCCGAGGTGGCGT[C/T]GTCGTCGAATGGATT | 11252 |
| rs764295552 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903907 | CTGTATCCTCAAGTA[C/T]GAAGGTGAAGAAAAT | 11252 |
| rs764296688 | in-del | -/CATC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944607 | CTTGGACAAAATGTT[-/CATC]ACTGCAATATTTATA | 11252 |
| rs764317132 | snp | C/G | 1.72009e-05 | 0.0029326 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893653 | GCAGGGGGCTTGGGG[C/G]AGCCTGTCCTTGGCT | 11252 |
| rs764327906 | snp | C/T | 3.32657e-05 | 0.0040782 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893577 | ACAGGCGGTGGCCAT[C/T]GTCGATCCGCTTCAC | 11252 |
| rs764329883 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954892 | AGAACAAACTGGTTT[-/G]GGATCTGATAAATAT | 11252 |
| rs764364689 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939479 | TGATTGGAAGTGACG[A/C]AGTTAGAGCAGGCCT | 11252 |
| rs764365461 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947411 | GAAGCAGGACTTCCT[A/G]TCACACAAAGGGCCT | 11252 |
| rs764389146 | snp | C/T | 1.66062e-05 | 0.00288146 | missense | PACSIN2 | GRCh38.p7 | 22:42879135 | TTCTTCTTCTCTCTC[C/T]GGCTGAGGGTTCGAT | 11252 |
| rs764398583 | snp | A/C | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015946 | AAGAGAGTAAATGGC[A/C]GAGCCAGGATTAGAA | 11252 |
| rs764416930 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935715 | TGAGAACAGGTTCAC[A/G]GGCCAGACACTGAAA | 11252 |
| rs764433654 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958991 | TACGTACATAAGGCT[A/G]CTCAGTTATTAAAAC | 11252 |
| rs764442975 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994636 | AATTCCAGGGTCTCT[A/G]TCCCTGTGCATGGCC | 11252 |
| rs764476908 | snp | C/T | 1.65919e-05 | 0.00288022 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871372 | TCACTGGATCGCCTC[C/T]ACATAATTTGCCGGG | 11252 |
| rs764488256 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919706 | TGAACCCGGGAAGTG[G/T]AGGTTGTAGTGAGCC | 11252 |
| rs764509434 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909375 | ACCTCAAGACCACAA[A/G]GCTTTCTTTGGAAAA | 11252 |
| rs764516227 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874631 | CTTCTCTGGCAGTTG[C/G]GGACCCCTAGAGAAA | 11252 |
| rs764540823 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974964 | ATCTCCTCTGCAGAC[C/G]CAGCTGACCTTTGAG | 11252 |
| rs764551637 | snp | A/T | | | intron-variant, missense | PACSIN2 | GRCh38.p7 | 22:42880621 | CAGACACTTACTTCA[A/T]CCTTGTGGCATGAAA | 11252 |
| rs764564463 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908218 | AGAAATCCCGCCTCC[A/G]GGGAGCTTTTGTTGA | 11252 |
| rs764565533 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947874 | GGAGAAGGTGACTGG[C/G]GCCAGGCTCCACGGC | 11252 |
| rs764596833 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993981 | CTGTGGTTTGCTGCT[A/G]GGACAAGTTCCATAA | 11252 |
| rs764601430 | in-del | -/ACCC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903158 | TTTATCCCTAAGCCA[-/ACCC]ACGTCCCAGGCAGCT | 11252 |
| rs764610903 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890144 | GTAGCTGGAACTACA[A/G]GTGCCCGCCACCACG | 11252 |
| rs764628691 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933213 | GGAAACAAACTATCT[C/T]TATGGTTCCATATAC | 11252 |
| rs764668989 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957006 | TGAAAATATAATAGT[A/G]AGTATAAAATGCTAA | 11252 |
| rs764678935 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997714 | CCAAATACAGGTCAA[-/C]AAAAATTAGCCAGGC | 11252 |
| rs764693375 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918849 | TTTTTTTTTGACACA[C/T]ACATGTCCTTAACCA | 11252 |
| rs764704017 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894748 | GTTTCATTCTTTTAG[C/T]TGCTGGCTTGAAAGG | 11252 |
| rs764708537 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934608 | CCTTGCTGGTCAACT[C/G]CCACCTACCTTGCAA | 11252 |
| rs764709037 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987706 | CCGGCTAATTTTTTG[C/T]ATTTTTAGTAGAGAC | 11252 |
| rs764752832 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988213 | AGAAAATGTAGGTTT[C/G]TCCCAGGCACCAAAG | 11252 |
| rs764752898 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000477 | GAGGTTTCTCTCTCT[A/G]CTCACCTCTTTACTT | 11252 |
| rs764769470 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899558 | CCAAGTGTGGGCAGA[-/G]GTGGGTGTACAGCAC | 11252 |
| rs764815519 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015563 | TCTCCCAAGGGACTC[A/G]AAGAAGCTAATGTCG | 11252 |
| rs764817738 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881666 | AATGAAAGCTTAGAC[A/C]CACATGATGGGAAAA | 11252 |
| rs764855768 | snp | C/T | 3.42425e-05 | 0.00413764 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884362 | CTTCAATGACGTGTG[C/T]GTTTTAGCTCAAAGG | 11252 |
| rs764859128 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908098 | TCCCCAAATACTCTT[-/C]TCAGGGGCTCTTTGT | 11252 |
| rs764865923 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999395 | TGTCTACAGGCCAGG[C/T]GTGGTGGCTCATGCC | 11252 |
| rs764871078 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880773 | GGCTCTGGCTGGGAC[A/G]CCCTCCAGGAGACAG | 11252 |
| rs764894867 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993595 | ATACAGAAAGAGCCC[C/T]TCCCAAGAAAGGGCA | 11252 |
| rs764906353 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899080 | AAGCTCTGTGGTGCT[C/T]CCAACCCCTAATACC | 11252 |
| rs764909140 | snp | C/T | 3.33506e-05 | 0.0040834 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42882277 | TGCTCTGATGCTCTG[C/T]TCCAGGTCATGGTAA | 11252 |
| rs764917365 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907118 | CCAGGCAGGGTCACA[A/G]ATCTTTGTGGATGGG | 11252 |
| rs764934620 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956271 | TCAAAATAAAATATG[C/T]ACCATGAGCCCACAT | 11252 |
| rs764939631 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878939 | CCACAGAGCTCAGGA[G/T]CCCAGGAACCTCCCA | 11252 |
| rs764940256 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986413 | CCAAACGAAATCAAA[C/T]GCCTAAAAGAAATGA | 11252 |
| rs764940555 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913979 | TGCTGTGCAGCAACA[C/G]AGACAAAGTCCACAA | 11252 |
| rs764981997 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967685 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 11252 |
| rs764984125 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946062 | TCCTATCAGCTCCAC[C/G]CCTTCACACACACTG | 11252 |
| rs764991479 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889056 | TTTGTGAAGCTTTCA[C/T]TTGAGTTGCAGGAGG | 11252 |
| rs765062359 | snp | C/T | 1.656e-05 | 0.00287745 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888712 | TTCAGGGTTGAGGGA[C/T]GGGTCTGCCTTGCTG | 11252 |
| rs765075444 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952243 | AGTCAAGGAATGACA[C/G]AGCATAATTCTGTTT | 11252 |
| rs765096167 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994816 | GGCTGCGGGGAGCAC[C/T]CTAGCATATCCACAC | 11252 |
| rs765124606 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961993 | CCACGGCACCATCAC[-/A]GAAGATGAACACCAG | 11252 |
| rs765130756 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878145 | GATTGTGCAGCAACC[C/G]TGGCCAGCCCAGGGC | 11252 |
| rs765133604 | snp | A/G | 1.65586e-05 | 0.00287733 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876952 | CCTCATCCTCGAAGG[A/G]GTTGTAGCTGGACTG | 11252 |
| rs765141670 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913139 | GAGGTGGGCAACAGT[A/G]GGCAAGTTACCTACC | 11252 |
| rs765172269 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984982 | ATTTGCTTGTTCTGT[C/T]TGGCAACCAAAGGTC | 11252 |
| rs765223092 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887172 | ACCTGGGCTGCTTCA[A/C]AAGCCCAGATTCCTG | 11252 |
| rs765231319 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947985 | ACCTCCTCCAACACA[A/G]CGGCCAAGAGCTAGG | 11252 |
| rs765252175 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011625 | GAAGAAACAAAAGGC[A/C]AGGACATCTGCGAGG | 11252 |
| rs765258740 | snp | A/G | 4.99239e-05 | 0.00499594 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871491 | GACAAAGAGGGAGCC[A/G]TCTCCATGAGAGGTA | 11252 |
| rs765278440 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899591 | TTTACTGGATATACT[A/G]GTGGAAACAGACTGG | 11252 |
| rs765284640 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958162 | AGAAAGCAGATTACT[A/G]TAATGGAAAGAGTAA | 11252 |
| rs765298121 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920034 | GATCACTTGAGCCCA[A/G]GAGCTGGAGGCTGCA | 11252 |
| rs765320586 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000806 | GATTATATCCTTTCA[C/G]TCAGTCTTCATAAAA | 11252 |
| rs765323269 | snp | A/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004795 | CCAGGCAGAGGCCCC[A/G/T]TCACAGGCCTCCCTG | 11252 |
| rs765344549 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894905 | TCTCTTTGCCTGGCC[C/T]TGCACAGAGATGGGC | 11252 |
| rs765349081 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969629 | TTTCCCTTCTCCTAC[A/G]TAGTTTCTACGTAGA | 11252 |
| rs765369455 | snp | A/G | 3.31389e-05 | 0.00407042 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912007 | CATTCACTGGAAGAA[A/G]GCAGGTGCATTACCT | 11252 |
| rs765415924 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964844 | CTGGCCCAAGCCAGG[A/G]GTAACTAGAATAGTG | 11252 |
| rs765416133 | snp | C/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896325 | AGACTGATCCATGTT[C/G]CTATCTACGTCAGAA | 11252 |
| rs765436716 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984272 | CTACCACCCACTACC[C/T]AGCACTTAGCACTTT | 11252 |
| rs765464719 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904005 | CAATCATAAAGACAC[A/G]CTGAGTTACGAATCT | 11252 |
| rs765467534 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005745 | TGACCAGGCACACAT[G/T]CTGGGCTCCTGGGGT | 11252 |
| rs765504887 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013804 | CAGGCAGTATTTGGT[A/G]AACAGTGTACCAAGT | 11252 |
| rs765508708 | snp | C/T | 1.66338e-05 | 0.00288386 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912111 | GGGAGCAGCAAAGTA[C/T]ACTTAGTCAGGGGTC | 11252 |
| rs765562564 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996532 | GCAAGACTCTGCCGC[-/AAAA]AAAAAAAAAAAAAAA | 11252 |
| rs765565118 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931257 | CTTGCTGCAAACCAG[C/T]TGGGTAACCAGGGGC | 11252 |
| rs765576784 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927173 | ACTGTCCTTGCAGCC[A/C]ACAAGCCATCCTGTG | 11252 |
| rs765620550 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995555 | TGGTGTGGAAAAACC[-/AG]AGTGTGTATACAACT | 11252 |
| rs765636499 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910655 | TGGCTGTCACTGCTC[C/T]TGTCACTCTTGCTGT | 11252 |
| rs765655189 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901551 | TCTCCGTATATTTCT[A/G]CCCTTTCAGTTGTCA | 11252 |
| rs765666992 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937318 | CCCCAGCAAAAGGCA[A/T]GAGAGGCCCACCTGG | 11252 |
| rs765670881 | snp | C/G | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016571 | GAGAATCACTTGAAC[C/G]TGGGAGGCGGAGGTT | 11252 |
| rs765678273 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976739 | CACCAAACCCAGGTC[C/T]AATCATTTCACAGAT | 11252 |
| rs765680064 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948085 | CAGTGGGAATTCTTC[A/T]GCAGGAGCAGCAAGG | 11252 |
| rs765700291 | snp | A/G | 4.96775e-05 | 0.0049836 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891076 | CTTGATCTTCTCGAA[A/G]TCATCGTTCATCAGT | 11252 |
| rs765731322 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977495 | AGAATGGTGAAAAAC[A/G]GTTTTTAGTTAAAAA | 11252 |
| rs765737120 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948831 | TTTCGTGTGACAAAC[C/T]GATAAATGAATTCTA | 11252 |
| rs765769171 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004879 | AGGCAAAACCACTCA[C/T]CCCTTTAGCTCTGAC | 11252 |
| rs765787751 | in-del | -/CTT | 0.000265631 | 0.0115215 | cds-indel | PACSIN2 | GRCh38.p7 | 22:42879119 | GACGCCGTCAGTGGC[-/CTT]CTTCTTCTCTCTCCG | 11252 |
| rs765797649 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909502 | CTGAGCAGTCACTCC[A/G]CCACTCAACGAACAT | 11252 |
| rs765824442 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994932 | CACCCCAAGCCCCAG[A/T]CTCTGTCTCACTGGA | 11252 |
| rs765861235 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963213 | TGCCCCGGCCCACAA[C/T]GTACAGGCTGAGCAG | 11252 |
| rs765865467 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900728 | ATCCTCCCAACTTGG[A/G]CTCCCAAAGTGCTGG | 11252 |
| rs765905153 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963761 | CTCTCTACCACACCC[A/G]TGCCTCCCATGGAAC | 11252 |
| rs765930649 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005513 | CTGTAAGTGCCAGGA[C/T]ATGAGGGGAGTCCAT | 11252 |
| rs765945510 | snp | C/T | 1.69908e-05 | 0.00291463 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884372 | GTGTGTGTTTTAGCT[C/T]AAAGGAAACTTACCC | 11252 |
| rs765986788 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930345 | AACATGCAGCAGCAC[C/T]AGGACCTCTGGGTTT | 11252 |
| rs765990163 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973942 | ACCAAGAACAGAAGC[A/G]TAGCCTTAACTTGTA | 11252 |
| rs765996116 | snp | G/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873093 | GCTAATTTTGCATTG[G/T]TAAAAAGCAGGATAA | 11252 |
| rs766040797 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887293 | GCTACACCGACGGCA[C/T]AGCAGTGAGGAACAG | 11252 |
| rs766046603 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936974 | ATTTACACCCATTGC[A/G]AATGCATTAGTAATC | 11252 |
| rs766046662 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965442 | AAGGCGGGAGAAGGA[A/G]GGGAAAAGAAGGTGA | 11252 |
| rs766058520 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015856 | ACTGCTTCATGTCAT[C/T]CAGGTGGAGAGGATG | 11252 |
| rs766069978 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869989 | ATAGCTGGTGACGGC[A/G]GCGGGCACTGCTGAG | 11252 |
| rs766076331 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908077 | GATACTTATGTTCTC[C/T]TCATCTCCCCAAATA | 11252 |
| rs766135549 | snp | C/G | 1.6596e-05 | 0.00288058 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877053 | TCCCAGCTCTGCAGG[C/G]GCCCGTGAGGGTCCT | 11252 |
| rs766136663 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991552 | GGAGAGAGACTGTGC[A/G]GGAATCCAGCGGGCA | 11252 |
| rs766139959 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923154 | AGTTTTGTACCCATG[A/C]TACTGGTTTTAAAAA | 11252 |
| rs766160625 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954328 | CAGCCCATTGAGCCT[A/C]TAGTCTTGGGCTGTC | 11252 |
| rs766193578 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941845 | GCAGTGGCGCATTCT[C/T]GGCTCACTGCAACCT | 11252 |
| rs766224580 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922093 | ATGACTGAGGTATTG[A/T]AAACAGTTCCAGATC | 11252 |
| rs766225196 | in-del | -/AG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897938 | TGGAACACAGAACAC[-/AG]GGAGCAAATGGCAAT | 11252 |
| rs766309322 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969723 | GCATGATGATCGCTC[A/G]AGTCCACGTGTTCGA | 11252 |
| rs766311270 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985201 | GGAGTGGCGGCACAT[A/G]CCTGTAATCCCAGCT | 11252 |
| rs766311783 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926624 | AGAGGGGGGAAAACA[C/T]ATCTTGTTTCACTCA | 11252 |
| rs766312969 | snp | C/G | 1.66963e-05 | 0.00288927 | missense | PACSIN2 | GRCh38.p7 | 22:42876139 | GGAGCCCACCTACCA[C/G]CCTTGAAGCTCAGCT | 11252 |
| rs766410187 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995959 | GGCGTGGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 11252 |
| rs766418788 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002651 | GGCTTTCAAAACACT[C/G]TTAAGGTGTTCATAC | 11252 |
| rs766427950 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888900 | GCTACCAAGAGGGGA[G/T]AAAAAGGCAGGTACA | 11252 |
| rs766475548 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960209 | TTTGGGATCCTCCTG[A/C]TTACAAGAGAAAAAA | 11252 |
| rs766528549 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42949004 | TTTCCCTTAAACAAG[G/T]GGAGTGGGTCAGGCA | 11252 |
| rs766545915 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42897465 | GCAGAAAACTTTAGG[C/T]AGAAACTGAATATAA | 11252 |
| rs766579102 | in-del | -/ATAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012154 | TCTCAAAATAAATAA[-/ATAC]ATACATACATACATA | 11252 |
| rs766599075 | snp | A/C | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896579 | GGGAATTATGAATAA[A/C]GAAGCTATAACGTTC | 11252 |
| rs766635278 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922363 | CAGACAAAAGAACAG[A/G]TCATTTTTTAGGCCA | 11252 |
| rs766651716 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970617 | AAATAATAATACAAA[A/C]GTTTAACGAACATTC | 11252 |
| rs766681987 | snp | C/T | 1.65597e-05 | 0.00287743 | missense | PACSIN2 | GRCh38.p7 | 22:42888732 | CTGCCTTGCTGTTGG[C/T]TTCTCGTGAGATAGC | 11252 |
| rs766695952 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010930 | ACTTGTGCTCTTTGG[G/T]GGCCACTGTCCCTCA | 11252 |
| rs766708002 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892229 | GAGCCACAACGGAGC[C/T]GGGGCAGAAATCGAG | 11252 |
| rs766727003 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007959 | TGAAATGAAAATAAA[A/C]AGCAGGTACTTCCAC | 11252 |
| rs766730435 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977574 | TACAACATCTAGCAC[C/T]GGTGGAAATGCCCAG | 11252 |
| rs766734571 | snp | C/T | | | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876916 | TGTCGTCCTTCTCAC[C/T]GACGGTGCTGCCCGT | 11252 |
| rs766750375 | in-del | -/TAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989871 | GGGGAAAAAAAAATA[-/TAT]ATATATATATATACA | 11252 |
| rs766765117 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902085 | TGTGTGAAGGGCCAC[A/G]AGGCCCTAGGGATAT | 11252 |
| rs766791404 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928876 | CATCCCAAATTTGCC[A/G]TTAAACAGCAATGGG | 11252 |
| rs766838768 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966198 | AAAATGGTGAAACCC[C/T]GTCTCTTTGAAAAAT | 11252 |
| rs766844086 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006810 | ACAAGAGCAAAATTC[C/G]GTCTCAAAAAAGAAA | 11252 |
| rs766850379 | snp | A/G | 1.65732e-05 | 0.00287859 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882157 | CTCTTCCAGGCTGAT[A/G]AGCTCATGGGCACAC | 11252 |
| rs766879452 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928039 | TTCCACTTCTGTCCC[A/G]CTGTTTCCCTGAGGC | 11252 |
| rs766888028 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955768 | TGAACCTGAGGTGAC[C/T]GTCCCTATAGATGGG | 11252 |
| rs766971180 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006609 | CGTTTGAGGTCAGGA[C/G]TTTGAGACCAGCCTG | 11252 |
| rs766980223 | snp | A/G | 5.0119e-05 | 0.0050057 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871511 | CATGAGAGGTATGAC[A/G]CCGACGGTGGGCTAC | 11252 |
| rs766988813 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884508 | CATGTTCTCCATGTA[C/T]TGGGGTGTGCCCTGG | 11252 |
| rs767014513 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911877 | CCAAACCTTTTCTGC[C/T]GCTATCTAGGTCTGA | 11252 |
| rs767015045 | in-del | -/CTTCAAGTGCC | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995682 | ATACAGATTTGGTAA[-/CTTCAAGTGCC]TATAATGTCCACCAG | 11252 |
| rs767069627 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915162 | GATGAGCCACCACAC[C/T]GGGCCTAAGATTTAA | 11252 |
| rs767089441 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989900 | TACACACACACACAC[-/AT]ATATGTATATATATG | 11252 |
| rs767101116 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879195 | GGTGCCGAGGGAGAG[A/G]AACCAAAGGTTCACT | 11252 |
| rs767115003 | in-del | -/GA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971843 | GCCCCGTCCGGGAGG[-/GA]GGTGGGGGGCAGCCC | 11252 |
| rs767147125 | in-del | -/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872471 | TAACTCTCTTTGGCA[-/T]TTTTTTGGTCCATTT | 11252 |
| rs767163056 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012804 | ATTACAGGTATGAGC[A/G]CCACCACACCCAGCT | 11252 |
| rs767208647 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976390 | GCTCCAGACAGAGCA[C/G]AGGCAACACTGGCCA | 11252 |
| rs767219626 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928261 | GCCTCTGAAGTCCTT[A/G]AAGTGATTCACTGTC | 11252 |
| rs767225259 | in-del | -/AG | 1.65938e-05 | 0.00288039 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876845 | GAGAGGAAGAGAGAC[-/AG]AGTGAGCGCGGTGGG | 11252 |
| rs767242061 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874936 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAA | 11252 |
| rs767285164 | snp | A/G | 5.66321e-05 | 0.00532098 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871314 | CTGGCTGAGGCTCCT[A/G]GGCCCGCCGCCTCCG | 11252 |
| rs767359607 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933233 | GTTCCATATACCTCC[C/T]CAACTTTCCTTAAAT | 11252 |
| rs767379345 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905208 | AAAGAACTCTTTCTC[C/T]GCATTCAGAATGATG | 11252 |
| rs767396525 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943085 | CAACAATGTTTTGTA[A/G]TTTTCAGAATATAAG | 11252 |
| rs767396683 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970655 | CCTTTGCAAAAAGGA[C/G]TCAGGGACAATGTGG | 11252 |
| rs767405395 | snp | C/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921805 | GTGCAGTGGCGCGAT[C/G/T]TCAGCTCACTGCAAC | 11252 |
| rs767414644 | snp | C/G | 1.7047e-05 | 0.00291945 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893641 | ACCAGCTGGGAGGCA[C/G]GGGGCTTGGGGCAGC | 11252 |
| rs767416337 | snp | A/C/G | 3.29936e-05 | 0.00406152 | missense | PACSIN2 | GRCh38.p7 | 22:42884450 | CCCGGAAGAAGCGAA[A/C/G]GCGTTTCTCCTCGAA | 11252 |
| rs767489624 | in-del | -/CAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991812 | CTGGCTATCCACAGA[-/CAA]AAAAAAAAAAAAAAA | 11252 |
| rs767495279 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932369 | CCTTCTAACTCTTTT[C/T]ATATTTCCTCAAAGC | 11252 |
| rs767504993 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870123 | GCCCGAGACACTCGT[A/G]CTGCGGGTAAGACCC | 11252 |
| rs767522124 | in-del | -/CTA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965114 | ATAAAAAGGAATGAG[-/CTA]CTGACAGATGTGACA | 11252 |
| rs767563977 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977690 | GATGGGAGGTGATTA[G/T]ATCATGGAGGCGAAT | 11252 |
| rs767577902 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949099 | GGAGTTACAAACCAG[C/T]CTGAGCAACAAGGTG | 11252 |
| rs767604825 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978620 | CCGCACTGACGGTAA[A/G]TTGTGGGAGGCAGTC | 11252 |
| rs767621432 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877034 | AGAGAGAGCTTTCAG[A/G]GGATCCCAGCTCTGC | 11252 |
| rs767630808 | in-del | -/TTTA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925096 | AGACCCCCTCCCTGC[-/TTTA]TTTTTCTCTCCCAAG | 11252 |
| rs767657108 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966441 | AAGCCAAATGTCTAA[C/T]ATTCTCTATCAAAGA | 11252 |
| rs767668871 | snp | C/T | 1.65597e-05 | 0.00287743 | missense | PACSIN2 | GRCh38.p7 | 22:42888737 | TTGCTGTTGGCTTCT[C/T]GTGAGATAGCCAGCT | 11252 |
| rs767678623 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885958 | GGCAGCCCTGCATGG[C/G]AGCCTAGCTCAGAAG | 11252 |
| rs767685479 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939371 | TTACTTTAAAAAGGA[C/T]AAAAATGACACTTTT | 11252 |
| rs767703798 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912778 | ACACCTTGCTAGTGT[A/G]ATGACCTGTCCGCAG | 11252 |
| rs767710408 | snp | A/G | 6.63945e-05 | 0.00576132 | missense | PACSIN2 | GRCh38.p7 | 22:42882254 | CTCAGGTCCTCCACT[A/G]CATCAGCTGCTCTGA | 11252 |
| rs767731815 | in-del | -/TCT | | | cds-indel, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870548 | TGCTTGAAAAGTTAG[-/TCT]TCTTTTTAACTCTGA | 11252 |
| rs767733572 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884796 | AGACAGGTAGATGCC[A/G]GCAAAGGGCAGTCTC | 11252 |
| rs767796899 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992946 | AGGCGGGCAGATTGC[C/T]CGAGCTCAGGAGTTT | 11252 |
| rs767802918 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918747 | CCACCACCTGCCAGG[A/G]AGGCTGGAGCCTCAG | 11252 |
| rs767822829 | in-del | -/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922413 | CAAGAACATTCTGAG[-/TA]AAAAGACCATGTTGC | 11252 |
| rs767824990 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881851 | CATCCCACAGGGTGG[G/T]TCAGGGACCTGAGGT | 11252 |
| rs767832804 | snp | A/G | 3.31345e-05 | 0.00407016 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888827 | GAGTTCCTGAATGCC[A/G]TGTCACTGGGAGTTC | 11252 |
| rs767844079 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967523 | TTTAACTTTGTAACA[C/G]AATAATTATACTGTT | 11252 |
| rs767883768 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957875 | CCCATCGTGAGGCCC[A/G]CTTCTATCAGTAACA | 11252 |
| rs767918786 | snp | A/G | 0.000100043 | 0.00707189 | missense | PACSIN2 | GRCh38.p7 | 22:42879063 | CTGCTGGGCTTACTC[A/G]GCAGAGACTGGTCGC | 11252 |
| rs767963231 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997233 | AACCGTGCCTAGCAC[A/G]TGGCAGGCGTTCAAA | 11252 |
| rs767967459 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999545 | GTGGTGGTACATGCC[C/T]GTAATCCCAGCTACT | 11252 |
| rs767973304 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929038 | TATGGAAGAATAAAC[A/G]TGAATTAAAGCCGAG | 11252 |
| rs767989404 | snp | C/G | 3.32856e-05 | 0.00407942 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876150 | ACCAGCCTTGAAGCT[C/G]AGCTCATCATGCTCC | 11252 |
| rs767997712 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917985 | ACACTCAGTCCCAGG[G/T]CAACTGTATTTAAAT | 11252 |
| rs768035062 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946403 | CACACATTGGCCTCT[G/T]AGCCTGGCGAGAGCA | 11252 |
| rs768047230 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894576 | GTTCCAAGTAGGACT[C/G]TCTTGATGGCAAAGC | 11252 |
| rs768068973 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42877001 | GGGGTTGCTCGGGAC[A/G]TTAAGGGTGCTATGG | 11252 |
| rs768077406 | snp | C/T | 9.93921e-05 | 0.00704884 | missense | PACSIN2 | GRCh38.p7 | 22:42876218 | CCGTCCCCGAGGTGG[C/T]GTCGTCGTCGAATGG | 11252 |
| rs768081189 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009479 | TTAATCTGGGTCCAC[A/G]CCTATGAAGCTGTCC | 11252 |
| rs768083869 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888673 | CTTGCACTTTTCTAT[C/T]TTGTCTTGCAATTTC | 11252 |
| rs768146790 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894143 | CTCCCCTACCTAGTA[A/G]GAATAAGTGTCCCCA | 11252 |
| rs768150340 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902816 | ACAGGGCTTCGCCAT[G/T]TTGGCCAGGCTGGTC | 11252 |
| rs768153573 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903031 | AGAAGAGCAACTCCC[A/G]GCGCTTCTGCCGCAT | 11252 |
| rs768177553 | snp | G/T | 1.65619e-05 | 0.00287762 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888790 | GTGGGCTTTCTTTGC[G/T]GCTTCTACCTACAGG | 11252 |
| rs768180978 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008569 | TCAGTGTTCTTTTAC[A/G]TATATGAGCTCTTTA | 11252 |
| rs768181223 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939507 | CCTAACTGAACCAGA[A/T]CGATGCAACTCCACA | 11252 |
| rs768232192 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917706 | CCTATTTCCAGGCAC[A/G]GTCTGTCGATCTTGG | 11252 |
| rs768250622 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007663 | CTGAGGACAGTCAGA[A/C]CCGCCCTCCTCTGTC | 11252 |
| rs768258569 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956131 | TGATGGGAAACATGA[C/T]TGAGTATGAAATTCA | 11252 |
| rs768262271 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903462 | AACAGGGGTCCTTGA[A/G]AAACCATCTAGTCCG | 11252 |
| rs768265466 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951219 | TGGTAAAGGAATCCA[C/T]GAGCCTTATCTTCTA | 11252 |
| rs768277095 | snp | C/T | 3.31367e-05 | 0.00407029 | missense | PACSIN2 | GRCh38.p7 | 22:42882219 | TGGCCATGCCCGGCC[C/T]GTGATTGGCTCGGAA | 11252 |
| rs768278316 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979252 | TATTTGGCCAGGTGC[A/G]GTGGCTCATGCCTGC | 11252 |
| rs768282810 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929431 | CATTGAAGATGCTGT[C/T]AATAGCTTCTGAGAA | 11252 |
| rs768312732 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940043 | ATGGAATTATTCCCC[C/T]GGCCCCCTGCATCCA | 11252 |
| rs768326469 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973608 | GCTCTCCAGCCAACA[A/T]GCCTGCCTGTCTCCG | 11252 |
| rs768360295 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877586 | TTCTAGATAGAAAGA[A/T]GATTCCTTTGGTGCT | 11252 |
| rs768368482 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978401 | ACCTATAACGCTGAG[A/C]AATCTAACAGAAAAT | 11252 |
| rs768369333 | snp | A/C | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872818 | TCTGCCAGACCAGTG[A/C]GCCTGCAGATCTAAC | 11252 |
| rs768421126 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877833 | GCCAGCAGCACCTTC[C/T]ACTTCCAAGACCAGG | 11252 |
| rs768427201 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989412 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 11252 |
| rs768436588 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956961 | CTAAGAAAAGGAAGC[C/T]GATTGGAATATTCTA | 11252 |
| rs768443096 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919148 | GTATTTAATAATTAA[C/T]TGGGGGCTTCTCATC | 11252 |
| rs768483566 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012281 | GAGGCAGAGGAATCA[C/T]TTGAACCTGGGCAGA | 11252 |
| rs768490012 | snp | A/G | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42946933 | TGAAATTCTCTGTGC[A/G]GCTCCATTCCCCTTC | 11252 |
| rs768513527 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000027 | GATCCCCATTTCAAA[C/G]GTGAGGTAGGTATCA | 11252 |
| rs768524906 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015425 | TGGTCCTTGAGACGC[A/G]CTTCCCGGGGCTGGA | 11252 |
| rs768546314 | snp | A/G | 4.98128e-05 | 0.00499038 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912091 | GACATTTTTTCAAAG[A/G]CTGAGGGAGCAGCAA | 11252 |
| rs768584165 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910059 | GATTGGGAAATGAAG[G/T]CAAAGAAAAATCAGT | 11252 |
| rs768608262 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879578 | CCTGTGGCCTCCCCA[A/G]ATGTCTGCTGAGCCT | 11252 |
| rs768679993 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914656 | GAATAGCAGGGCTTT[G/T]GGCTCAGGTGAGTCT | 11252 |
| rs768680521 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907842 | TGTCCTATAGAATTG[C/G]TATGGAAGGATGGGG | 11252 |
| rs768714869 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976134 | GGGGCTAGAAACTAT[C/G]CCTGTGCTAATTCTT | 11252 |
| rs768725896 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979524 | GCAAGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 11252 |
| rs768766374 | snp | A/G | 6.62756e-05 | 0.00575616 | missense | PACSIN2 | GRCh38.p7 | 22:42876199 | AGGGCCCGGACTCGC[A/G]CTTCCGTCCCCGAGG | 11252 |
| rs768769642 | snp | C/T | 1.65594e-05 | 0.0028774 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876891 | TTGTTCACCAACTTT[C/T]TGGCCTTAGTGTCGT | 11252 |
| rs768814264 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996788 | GTGTCCTCAGGCCTG[C/G]CTTACTGAGTTCTAC | 11252 |
| rs768842317 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936402 | GGAGCAGAATGACCC[C/T]GGACTTAGCACAAGA | 11252 |
| rs768845502 | in-del | -/ACTC | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870400 | CAGTTTACAAACGAA[-/ACTC]ACTGTTAAAAGCTGT | 11252 |
| rs768882094 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012194 | ATACATACATACATA[C/T]ATACATACAAACATA | 11252 |
| rs768893527 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926474 | CCACCTCATGGCACA[C/G]AACTATCCACTGCAA | 11252 |
| rs768900248 | snp | C/T | 1.6679e-05 | 0.00288777 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891157 | GAAGGCCATCCAGGC[C/T]TTCTCCACGGTCCCG | 11252 |
| rs768910828 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884849 | CTTGAGCGTGCCACA[C/T]GCCCATGTCCTCTTC | 11252 |
| rs768924999 | snp | A/G | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002364 | CTCACAACCTTGGGA[A/G]CGTGGAACATTAGCT | 11252 |
| rs769001546 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952935 | CCTCCCACAGTGTTG[C/G]GATTACAGGCGTGAA | 11252 |
| rs769032921 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001445 | TAAAAATGCAGCCCC[C/T]AAAGCATCAAGCAAA | 11252 |
| rs769034855 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870364 | CAGCCAGACGTGTGC[C/T]TGAATGCCACAGACT | 11252 |
| rs769053256 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959932 | TTTCCTGTTGGCTGC[C/T]GAGATAAGGTCATTC | 11252 |
| rs769060994 | in-del | -/CCGCCTCCGTCCCC | 1.98312e-05 | 0.00314884 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871321 | AGGCTCCTGGGCCCG[-/CCGCCTCCGTCCCC]CCGCTGGCCTGTCCC | 11252 |
| rs769066756 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005323 | AGGCTTTCTAGAATC[C/T]ATCACATTAAACTCA | 11252 |
| rs769066783 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891251 | GCTCTGCTCACACCT[C/T]GGCTGTTCAATGTGG | 11252 |
| rs769109655 | in-del | -/TAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012160 | AAATAAATAAATACA[-/TAC]ATACATACATACATA | 11252 |
| rs769127807 | snp | C/T | 1.66863e-05 | 0.0028884 | missense | PACSIN2 | GRCh38.p7 | 22:42890960 | ACCTCTTTCAGCTTC[C/T]TGGCCCAGGGCTTCT | 11252 |
| rs769151735 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984892 | AAGCAGCTGGGGAGA[G/T]GTTGGAAAACAAAAG | 11252 |
| rs769162988 | snp | A/C | 4.94474e-05 | 0.00497205 | missense | PACSIN2 | GRCh38.p7 | 22:42884478 | GAACTGCTGGCACTG[A/C]TCAAACACCTGCTCC | 11252 |
| rs769164931 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991008 | AGGACTCAACGGGTT[A/C]TATACACAAAGTGCT | 11252 |
| rs769180117 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009771 | CCACCACACATGCAC[C/T]TTCCAAAGGTACAGC | 11252 |
| rs769191346 | snp | C/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897083 | CTGGAACTACAGGTA[C/T]GCACCACCACACCTG | 11252 |
| rs769203589 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907188 | GCTTCTCAGGAAGAG[A/C]CAGGGAGTCCAGCTG | 11252 |
| rs769216801 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915508 | CAATGAGGGACAAGC[A/G]TACCCCACGGGTATC | 11252 |
| rs769238880 | snp | A/G | 0.000102173 | 0.00714675 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879038 | TTGGATGGAGGTGGC[A/G]CCCACTCACCTGCTG | 11252 |
| rs769272642 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968241 | AACATCTGTTTCACT[A/G]TTGTTGTTTTGGGGA | 11252 |
| rs769277710 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872942 | GTTTCTTTTGTCCTG[C/T]CTTCATTGGTTGCTG | 11252 |
| rs769281404 | in-del | -/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959947 | CGAGATAAGGTCATT[-/C]CCATACACTGCTGCA | 11252 |
| rs769284081 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883394 | GGAGACAAACGGAAT[A/G]TGTCTCCTATTAACA | 11252 |
| rs769285027 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894431 | TATTTTTAGTGGAGA[C/T]AGGGTTTCACCATGT | 11252 |
| rs769305031 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939185 | AACTCGTTTATCTTA[C/T]GCAATGGGAACACAT | 11252 |
| rs769312077 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987980 | ACCCCGTCTCTACTA[A/G]AGATACAAAAATTAG | 11252 |
| rs769329833 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959396 | TCGGTAAGAAAAAAA[C/T]ACAGCTAAAGTATGT | 11252 |
| rs769341902 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969000 | TCAGACTCTACAACC[A/G]TGTGAGCCAATTCCC | 11252 |
| rs769406461 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940774 | TTCTGGGTATACAAA[C/T]GGAAAAGACCCAAAT | 11252 |
| rs769411250 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919383 | CAGACAAATGAGTCA[C/T]CCCTGGTCTTTCCAA | 11252 |
| rs769414581 | in-del | -/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869660 | GTGGCCTTTTGGGCA[-/G]GGGGTCCTGTGCCCT | 11252 |
| rs769424626 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957089 | CTCCTGAGCCTGCAG[C/T]CCCACTTCTTCTCTA | 11252 |
| rs769459962 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930237 | GAATAAACTTCTCTT[A/T]AAGCCACTATTATTT | 11252 |
| rs769477857 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958741 | AACATCCTAACAAGA[A/T]AGCATGTTTTTCTGT | 11252 |
| rs769479702 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947226 | TTCACAGGCGGCAGA[C/G]TGAGCAGGAAGGAGG | 11252 |
| rs769488198 | snp | C/G/T | 0.000117189 | 0.00765389 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871336 | CCGCCTCCGTCCCCC[C/G/T]GCTGGCCTGTCCCCG | 11252 |
| rs769546141 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926535 | TCTTAGGAACTCCAC[A/G]AGGACACAGAATCAC | 11252 |
| rs769563455 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990697 | CAACGGGTAAGCAGG[A/G]GTCAGACCACAAGTC | 11252 |
| rs769577859 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910038 | CGTTATTACCCCCAT[C/T]TTATAGATTGGGAAA | 11252 |
| rs769588178 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999896 | GTCCCAAGGCAAGAT[-/G]GTTGGCAGGCTCAGA | 11252 |
| rs769625380 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009721 | GGAAAAATAATCATA[C/T]AAATTTTATCTGGCC | 11252 |
| rs769626312 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964334 | GAGGCAGGAGAATTG[C/T]TTGAACCCAGGAGGT | 11252 |
| rs769627114 | snp | A/C | 1.67987e-05 | 0.00289811 | splice-acceptor-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893614 | CTTGTAGTTCCCGAC[A/C]TAGGAGAGAGAACCA | 11252 |
| rs769636850 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936608 | TTACATATATCAAAG[C/T]AGAAATAAAGATGGG | 11252 |
| rs769682543 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005380 | AGCAAGGCCTCTCTG[C/T]ATGGCAAGGCTGCCC | 11252 |
| rs769685897 | snp | G/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016513 | ATTAGCTGGGTGTGG[G/T]GGCATGCACCTGTAA | 11252 |
| rs769701358 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937528 | CTGCCTAGATGTCCC[A/G]GCTCGATCACCAAGG | 11252 |
| rs769704826 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890584 | TTAGCAGGGTGTGGT[A/G]GCATGTGCCGGTAGT | 11252 |
| rs769757307 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901260 | GGCAAGCCCATGGAA[C/T]CAGAGTCAAATGTTT | 11252 |
| rs769785367 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895036 | GGTGAAAAGCAAAGA[C/T]CCCTGGAAGGTGGTT | 11252 |
| rs769799195 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880341 | TAATTATTTTCTGAC[C/G]AAAATAGATTGACTG | 11252 |
| rs769799478 | snp | G/T | 1.72794e-05 | 0.00293928 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893420 | GGCTGGGGTGTAGCT[G/T]CCTCCAGGCCACAGG | 11252 |
| rs769801529 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944381 | ACTTCCTTTAAAATA[C/T]GGAAATAACTTGTAA | 11252 |
| rs769806992 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970443 | TAGTTTATTCAGTAA[C/T]ACTGCATCAATGTTA | 11252 |
| rs769810432 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900565 | CAGAGGCGCAACCTT[C/T]CCGTCCGAAGTGATC | 11252 |
| rs769814543 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947711 | GATCCAGCTGCCTCA[A/G]GCAAAATACCTAAGA | 11252 |
| rs769869806 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949460 | CTCATACACACACGC[A/G]CGCGCACGCACACAC | 11252 |
| rs769969045 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987494 | ACACACACACACACC[-/A]CATGGCACCATGTTC | 11252 |
| rs769997698 | in-del | -/TGAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951116 | GCCATAAGAATACAC[-/TGAT]TGAGTTGCTTTTGAA | 11252 |
| rs770004906 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879704 | CAAGACAGTTGGCTT[C/T]GGAGACCTGAGCAAG | 11252 |
| rs770023768 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914843 | TGACACAGTTCTGCA[C/G]AAGACTGATTGATTG | 11252 |
| rs770035090 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985732 | TCTTCACCACATTAT[A/G]TTCAGAGGGAGGGCT | 11252 |
| rs770087138 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891565 | GCCACCACGCCTGGC[A/T]AAATTTTTGTATTTT | 11252 |
| rs770097063 | snp | C/T | 1.69542e-05 | 0.0029115 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876109 | GTTGGAAGCCCTCCT[C/T]CCCTGGATGCTGGGG | 11252 |
| rs770111453 | in-del | -/CCT | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894360 | ATTCTTCTGCCTCAG[-/CCT]CCTCAGTAGCTGGGA | 11252 |
| rs770114679 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962055 | CACTCCACTAAGACA[A/G]AAGCAGCGCCTGAGT | 11252 |
| rs770147637 | snp | G/T | | | missense | PACSIN2 | GRCh38.p7 | 22:42884498 | ACACCTGCTCCATGT[G/T]CTCCATGTACTGGGG | 11252 |
| rs770202685 | snp | C/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897242 | GCGCCTGGCCTGTTC[C/T]CTTTTTAATATATTT | 11252 |
| rs770205322 | in-del | -/TAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989869 | AGGGGGAAAAAAAAA[-/TAT]ATATATATATATATA | 11252 |
| rs770225934 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957497 | ACTGTTCTCAGCATA[-/C]CTGTTTATAACTAAC | 11252 |
| rs770228456 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985624 | TGCAAAACATAAAGA[C/T]AACAGGACAAAGAAC | 11252 |
| rs770229984 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885454 | TATGGGGGTAGTCAC[A/G]GGCTCCACTCAGGTC | 11252 |
| rs770230162 | snp | A/G | 1.67119e-05 | 0.00289062 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884567 | TCTCTTTGGTCTAAA[A/G]GAAAATCCAGGCACA | 11252 |
| rs770230323 | snp | A/G | 1.70539e-05 | 0.00292005 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876382 | ACAGGGCGGCAGAGG[A/G]TGTGAGGCCCCCGCC | 11252 |
| rs770234968 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960109 | TGAGAACAAAATTCA[C/T]ACTACCCCCTCCCCA | 11252 |
| rs770273314 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876798 | GCTCCGTGCATTGCC[A/G]AGTGCCGAGGGGTGA | 11252 |
| rs770283214 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898588 | GAACCTCCTTTCTAG[A/G]GTCCTCCGGAGGCCG | 11252 |
| rs770283417 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880417 | ATAAATTCATCCTGA[A/T]TGGGTGGCTTCCAAA | 11252 |
| rs770285503 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924045 | AGACCTGGTCTCTTT[-/A]AAAAAAAAAAAAAAA | 11252 |
| rs770314133 | snp | A/G | 0.000182127 | 0.00954098 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876905 | TTTGGCCTTAGTGTC[A/G]TCCTTCTCACTGACG | 11252 |
| rs770335604 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879189 | GCAACAGGTGCCGAG[A/G]GAGAGAAACCAAAGG | 11252 |
| rs770352148 | snp | A/G | 1.65751e-05 | 0.00287876 | synonymous-codon, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871444 | GCCCTGCTCATCCTC[A/G]TCCTCCATCTTGGTC | 11252 |
| rs770357673 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959143 | GATGGGAAGGTGGTC[A/G]GGAGGGGTCCTGGAG | 11252 |
| rs770396026 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933036 | GCTGTATCATTGAAT[C/T]AGCATTTATATTTAC | 11252 |
| rs770399412 | snp | C/G | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002405 | ATCATCAAGTAGTAA[C/G]GATTTTCTAAAACAG | 11252 |
| rs770416825 | snp | C/T | 1.66518e-05 | 0.00288542 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871348 | CCCCGCTGGCCTGTC[C/T]CCGACTCATCACTGG | 11252 |
| rs770443952 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958862 | TTCACTGAGTGATGG[A/G]TCACTTAAGTATCAG | 11252 |
| rs770450919 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922051 | TTTGTTCTAAGGGGC[A/C]CTTCTCAGGAATCTG | 11252 |
| rs770452593 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875519 | GGACTACAGGCATGT[A/G]CCACTAAAATTAGCC | 11252 |
| rs770466280 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931851 | AATGTCACAAAACCC[A/C]CAATTGTAAGGAACA | 11252 |
| rs770470369 | snp | A/T | 1.65765e-05 | 0.00287888 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911973 | AAGGGCCTGCCAGAC[A/T]CTATTGGCCTGGCCA | 11252 |
| rs770486308 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42910258 | CAAGGCAGGGAATGA[C/T]TGGTGCCAGCCAGCA | 11252 |
| rs770520836 | in-del | -/CAAA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996531 | AGCAAGACTCTGCCG[-/CAAA]AAAAAAAAAAAAAAA | 11252 |
| rs770590477 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956426 | TGACATGCAAATGCA[C/T]TTAGACCACCTAGTG | 11252 |
| rs770625032 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948698 | TTTGGTTTTCAAATA[G/T]TTTCTGGGCATCTAT | 11252 |
| rs770651404 | snp | C/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896935 | TTCTTGAGTAAAGTT[C/T]GTTCCTTTTTTTTCT | 11252 |
| rs770674964 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892073 | GCAGGAGCCTGCTCT[A/G]GACCAGTATGGCAGG | 11252 |
| rs770685655 | snp | A/G | 1.65822e-05 | 0.00287938 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912070 | ACGGAATCATCATAT[A/G]TGACAGACATTTTTT | 11252 |
| rs770691822 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928518 | AAGCCTCATTTGTGA[A/G]ATTTTAGATGTGAAA | 11252 |
| rs770706895 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965723 | ACCAGGCTAGCTTGG[A/G]TTCTTCCCACTAGCA | 11252 |
| rs770718400 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982004 | GAGGGAGGTGGGGGG[-/T]GTCAGCCCCCCTTCC | 11252 |
| rs770764126 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955398 | ATCTAACGGATGGCT[A/G]GAAATAAGCCCAGAG | 11252 |
| rs770769895 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001302 | GACCAGAGGCTTCCA[C/T]GAAGCCCCTGCCAGA | 11252 |
| rs770774273 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | PACSIN2 | GRCh38.p7 | 22:42884494 | TCAAACACCTGCTCC[A/G]TGTTCTCCATGTACT | 11252 |
| rs770788339 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970984 | CTCTCTGCTACAGCC[C/T]ACCCCTGCACCACCT | 11252 |
| rs770797475 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927613 | TATTTTTGAGACTGA[A/G]TTTTGCTCTTCTTGC | 11252 |
| rs770816163 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914815 | AGATTCTGTCTGGAT[C/G]CAGCTGTGGTCTTGA | 11252 |
| rs770844621 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006461 | AATTACCTTTCTTCT[A/G]TAGGAACTAACAGTG | 11252 |
| rs770860591 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911212 | CCCGGCCATGCAAAG[C/T]CTCTTTCCATGAAGG | 11252 |
| rs770883501 | in-del | -/A/G/T | 0.00110485 | 0.0234786 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871334 | GCCGCCTCCGTCCCC[-/A/G/T]CCGCTGGCCTGTCCC | 11252 |
| rs770891387 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013408 | CATAACCTCACCAAA[A/G]AGGCTACCAAACTCT | 11252 |
| rs770920235 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887687 | AGCCCCTCCCTTCCT[A/G]TGAACTTTTAAATCA | 11252 |
| rs770925118 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881639 | AGGCCCTTGCATTTC[A/G]AATGTAAAGATAATG | 11252 |
| rs770944057 | snp | G/T | 3.56818e-05 | 0.0042237 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882343 | CTTTTAGAAGGCAGG[G/T]GCCAGCTACCCTTTG | 11252 |
| rs770956985 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960833 | GAGATCTGTGCACTT[C/T]AGGTATGCATATTAT | 11252 |
| rs771013226 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938655 | CACCATCTCCCTCTC[A/G]ACAGCCTGGCACAGT | 11252 |
| rs771023490 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969282 | TTTCAACAAATGATC[A/G]TGACATTACATGGTA | 11252 |
| rs771032217 | snp | C/G/T | 3.31369e-05 | 0.00407032 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876210 | TCGCACTTCCGTCCC[C/G/T]GAGGTGGCGTCGTCG | 11252 |
| rs771050624 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898615 | GCCGCTCTCCTGCCT[A/C]CCAGGGATGGACCTT | 11252 |
| rs771080048 | in-del | -/GT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014450 | AATCAGCGCACCCGC[-/GT]GTGTCCTGCGTCGCC | 11252 |
| rs771103562 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906913 | TTGTGGGTGTTCTCT[A/G]TAATTCTTACAACCA | 11252 |
| rs771105451 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955953 | TTTGTTAAACTAGCA[C/T]TACCAATCTATGTTA | 11252 |
| rs771119914 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988676 | ATGCAGTTCAGTTAA[C/T]ATTGCTCTCCAAACT | 11252 |
| rs771119963 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011973 | AACACGGTGAAATCC[C/G]GTCTCTACTATAAAT | 11252 |
| rs771121426 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972555 | CCATTTTAGAAAAAT[A/G]GTTCCTTATACATCT | 11252 |
| rs771149502 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944198 | ATCAGCCTGGCCTGA[C/G]GGACTCTGTGGAACC | 11252 |
| rs771154462 | snp | C/T | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871676 | CAGACCTAGAGATGA[C/T]AGTCTCACACAGTAA | 11252 |
| rs771198756 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933161 | GAGGAAAACCTTGTT[A/G]TCCCTGAAAAGTTGA | 11252 |
| rs771208357 | in-del | -/ATAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965911 | AAACCTACTATAATC[-/ATAA]ATAAATAAATAATCA | 11252 |
| rs771209475 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986015 | TGATTGGGCCAATGC[C/T]CCAGGTCAGGAGGCT | 11252 |
| rs771209600 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870734 | ATAGAAACCCGACCA[C/T]AACCCGGTCCCACCT | 11252 |
| rs771241301 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979424 | AGCTACTCCAAAGGC[A/T]GAGGCATGGGAATCA | 11252 |
| rs771250976 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869634 | CCTCCAGTTTGGCAG[A/G]GGCAGTGGGCCGTGG | 11252 |
| rs771257538 | in-del | -/TAAAAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005061 | ACTTAAACATTAATC[-/TAAAAG]TAAAAGGGCAATGGT | 11252 |
| rs771267957 | snp | C/T | 0.000132488 | 0.00813795 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876985 | ACTGCGCAGACTGGG[C/T]GGGGTTGCTCGGGAC | 11252 |
| rs771315266 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978440 | TCGTTTACACGCAAC[A/G]CAAGAAGAGCACAGG | 11252 |
| rs771365260 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004468 | AAGCATCACCACGTG[C/T]GAGCTAAGTGGCGAG | 11252 |
| rs771379020 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922518 | GCAGAGGTGGACATC[C/T]TCGCTGCCACGGCCC | 11252 |
| rs771384469 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902916 | ACCGCGCCCGGCCTA[G/T]TTATCAGTTCTCAAT | 11252 |
| rs771408323 | snp | C/T | 6.87971e-05 | 0.00586462 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893444 | CCACAGGACCTGTGC[C/T]GGGGCCCCATACCTT | 11252 |
| rs771412703 | snp | A/G | 1.66721e-05 | 0.00288717 | missense | PACSIN2 | GRCh38.p7 | 22:42893526 | ACGCCTTCTCGATGC[A/G]CGCCCGCTCATGCAG | 11252 |
| rs771421599 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962113 | TGGCCAACATGGTGA[A/T]ACCCCGTCTGTACTA | 11252 |
| rs771431924 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949684 | ACACACATACACTCA[-/CA]CACACACACACTCAC | 11252 |
| rs771468214 | snp | C/G | 1.70667e-05 | 0.00292114 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876091 | ACCGCCCACAGCCTG[C/G]AGGTTGGAAGCCCTC | 11252 |
| rs771479321 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913380 | GCTACTCAGGAGGCT[C/G]AGGCAGGAGAATCGC | 11252 |
| rs771508638 | snp | A/C/G/T | 5.12348e-05 | 0.00506117 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884607 | TTCATTTCCATTTAG[A/C/G/T]CCTTGGCTCACCCTG | 11252 |
| rs771512332 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42953827 | TATATGTGCCCTCTC[A/G]GAGGCAAGCGTGATT | 11252 |
| rs771512340 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980287 | GAGAGGCCAAGGCAT[G/T]AGGACTGCTTGAGCC | 11252 |
| rs771521723 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944267 | CGAGAAAGACATTTG[C/T]GTTAGGCTAAGTCTC | 11252 |
| rs771542758 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923099 | GTGCACTTTAGAAAG[C/G]ACTAATCTGGCATCA | 11252 |
| rs771567963 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875722 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTCACCAT | 11252 |
| rs771609372 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892147 | AGGCTCAGGAAGGAA[A/G]CCCTAATCCAGGCTG | 11252 |
| rs771622805 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901900 | TCCGTGGTTCAGCTC[A/G]GACCAGCTGGCTCGC | 11252 |
| rs771624903 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912460 | GTAGGGCTAGGACCC[A/G]GGATAAAACGTGAGT | 11252 |
| rs771646164 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876604 | CAGCACAGACTGCGC[A/G]TTGTCTGTTTTCCTG | 11252 |
| rs771648569 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966035 | GCTATTTGCAAATCC[C/T]ACTTGTTAGCCTTTC | 11252 |
| rs771697702 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993231 | TATGATTCCATTTAC[A/G]TAAAATTTTAGAAAA | 11252 |
| rs771765120 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949925 | AAACATTTACTTTCT[G/T]AGTGCCAGAAACCTT | 11252 |
| rs771783565 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992675 | GTAACATCTTTTCAC[A/G]ACATAGCATCTTCAT | 11252 |
| rs771791814 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885367 | GTTGGTGGGATCATG[A/G]TCGTGTTGTCCCCCT | 11252 |
| rs771803002 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881311 | GCCCCCGACAGGAGA[C/T]GGGTGCTCTTGTCAT | 11252 |
| rs771820316 | snp | A/G | 1.65669e-05 | 0.00287805 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888649 | ACAGTTTACCTTAAG[A/G]ACATCTTGCTTGCAC | 11252 |
| rs771838880 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920167 | AAAAAAAGAAACTGA[G/T]CTCCAATACCGGAAT | 11252 |
| rs771844760 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994666 | CTAAAGGGAGAGGCA[C/T]AAGTTTTAGGGAGAT | 11252 |
| rs771860211 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966952 | TTTATTTATAGTTTA[A/T]TTCAGCCATCTGACA | 11252 |
| rs771878141 | in-del | -/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895919 | CTGGAAGTCTCTATC[-/G]CCATAAACCACCAGG | 11252 |
| rs771885583 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882100 | CTAACATAGAGTCTA[C/G]AATGAGAAAGACATC | 11252 |
| rs771905297 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956017 | GGGAAGTTCAACATT[C/T]TGTCCTGTTAATTAC | 11252 |
| rs771924642 | snp | G/T | 1.66263e-05 | 0.00288321 | missense | PACSIN2 | GRCh38.p7 | 22:42891146 | GCCTCGGACATGAAG[G/T]CCATCCAGGCCTTCT | 11252 |
| rs771924693 | snp | C/T | 1.66067e-05 | 0.00288151 | missense | PACSIN2 | GRCh38.p7 | 22:42879121 | CGCCGTCAGTGGCCT[C/T]CTTCTTCTCTCTCCG | 11252 |
| rs771957117 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956764 | CCCCAGGGGGCTGCC[A/G]TTTAACCCCTTCTCA | 11252 |
| rs772010464 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889889 | AGAAAGAAAAATGTA[A/G]ACTAGTTCTTTCTAT | 11252 |
| rs772011563 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43004550 | GCTTGGACGTCTGTA[C/T]AGGGAGCACTGCCTG | 11252 |
| rs772038113 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974364 | TACTTCTAAACAGTA[A/G]GGAAGGATGCCAGCT | 11252 |
| rs772042938 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932604 | GATAATGTACTATTG[A/G]TATCAATTTTACTCA | 11252 |
| rs772085602 | snp | A/C | 1.65938e-05 | 0.00288039 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871473 | TCAGCTCATCCCCTG[A/C]AAGACAAAGAGGGAG | 11252 |
| rs772095441 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951837 | CCCCTGCTTCCAGCG[C/G]CAGTCTCGCTCCTTC | 11252 |
| rs772106538 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917422 | GACCAGCCTGGGCAA[C/G]ATAGTGAGATCCCAT | 11252 |
| rs772120562 | in-del | -/ACAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991811 | ACTGGCTATCCACAG[-/ACAA]AAAAAAAAAAAAAAA | 11252 |
| rs772125516 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877898 | ACTGCTCAGCCTGAG[C/T]ACCCACCACCCCAGA | 11252 |
| rs772125887 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888049 | AGTCCCTCCCCCAGG[G/T]CTCTGCCCCCAGCCC | 11252 |
| rs772166586 | snp | A/G | 1.68221e-05 | 0.00290014 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876364 | GGCCACAGGGCCCTC[A/G]GCACAGGGCGGCAGA | 11252 |
| rs772167223 | in-del | -/TATAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989869 | AGGGGGAAAAAAAAA[-/TATAT]ATATATATATATACA | 11252 |
| rs772181057 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887067 | CTGGCAAAGGCCCGA[C/G]AGTTCTCCCGGACCT | 11252 |
| rs772214429 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005144 | CTATCACTGCTGCGT[A/G]TTATCTTAATACAAT | 11252 |
| rs772248093 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946696 | TTCACACAGGCATGC[A/G]CACACACATGATCCT | 11252 |
| rs772276135 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973489 | ATTGAGAAAAAGACT[C/T]CAGATGCTTTCCCCA | 11252 |
| rs772276597 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962295 | CACAGGCTGCTCAAT[A/G]AACATTTACACAGCA | 11252 |
| rs772290067 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899398 | GTTTAAGCGATTTTC[C/G]TGCCTCGGCCTCCCG | 11252 |
| rs772303978 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869528 | AGAGAGGCGCCAGCC[A/G]ATGCCCGCACCATGT | 11252 |
| rs772323358 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963390 | TCAGCTCAGGCCCCC[G/T]GCAGAGGCGGCAAAC | 11252 |
| rs772331212 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949227 | GCTGACCTACACAGA[A/G]TAGGAATTTAAATGA | 11252 |
| rs772359272 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969394 | GTGATTTTTCTCCCT[A/G]AAAGATGTTAAGGAA | 11252 |
| rs772382702 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942388 | CAATTTACCCACTTT[C/T]TTCTTTTGTTGATTG | 11252 |
| rs772401288 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887569 | ATCCTGGTTGGGAAT[-/A]CTCCTCTCCAAACAC | 11252 |
| rs772425907 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962047 | CAAGCACTCACTCCA[C/T]TAAGACAGAAGCAGC | 11252 |
| rs772437540 | snp | C/T | 1.66471e-05 | 0.00288501 | missense, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893537 | ATGCGCGCCCGCTCA[C/T]GCAGGCAGTTCATGA | 11252 |
| rs772477232 | snp | A/G | 1.65644e-05 | 0.00287783 | missense | PACSIN2 | GRCh38.p7 | 22:42891018 | CCTTGGTCTCCTTGA[A/G]GCCGCCCATCATCTG | 11252 |
| rs772495795 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941977 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 11252 |
| rs772500652 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995344 | AACAGGCTGCTTTTG[A/G]TGCCAGGAGGACGGC | 11252 |
| rs772500816 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979638 | GCCCAGGTCAGATAC[A/C]TCCTTCTCTATGAAT | 11252 |
| rs772500822 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878473 | TCCTCTAGCACACAC[C/T]TTCCAGAAGGTTCTA | 11252 |
| rs772517717 | snp | C/T | 1.66125e-05 | 0.00288201 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884400 | CCCAGCCACATTGGA[C/T]AGGTCTAGGTGCTTC | 11252 |
| rs772538502 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009807 | CTCTAGCCTTATTTA[C/T]CATTTTTAAGGCTTC | 11252 |
| rs772546231 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909196 | CCTAGCAAATCCTAC[A/G]GCACCTGGCATGATG | 11252 |
| rs772552108 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989699 | GCTACTTGGGAGGCT[A/G]AGGTAGGAGAATCAT | 11252 |
| rs772573234 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011290 | CCTAACTGGAAAAAA[A/G]CTAAGCCAGCACTAT | 11252 |
| rs772575285 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000408 | TGAGTTTGTCTCCAC[C/G]TCCACCAATCACACT | 11252 |
| rs772616672 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926309 | GCTCAGCAGGTCCTA[A/G]GCCCTCCAGAAGCAC | 11252 |
| rs772621993 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935332 | TCCCCTGACCTAACT[A/C]ACCATTTCTCTCCTT | 11252 |
| rs772635520 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885309 | CGCACCCCCTCATCT[A/C]AGCATGCAGGGCCAC | 11252 |
| rs772654768 | snp | A/C | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43015747 | CTCACAATCACCTTG[A/C]ATGATAGGGTATTAG | 11252 |
| rs772655563 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964362 | GGTGGAGGTTGCAGT[A/G]AGCCAAGATCGTGCC | 11252 |
| rs772668592 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883412 | TCTCCTATTAACAGC[A/G]AGCCTTGACCCGTGA | 11252 |
| rs772669590 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42952758 | ATCTCTGCCTCCCAG[A/G]TTCAAGCAATTCTCC | 11252 |
| rs772674760 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906575 | TGTCCACTATAGCTC[-/A]GGGGGAGGGTCACCC | 11252 |
| rs772726813 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939935 | TTCTAGAGACTGCAT[-/G]TTAGTGGCAATCGGC | 11252 |
| rs772772506 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872961 | CATTGGTTGCTGTGC[C/T]CTCACAGGCCTGGAT | 11252 |
| rs772795306 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930254 | AGCCACTATTATTTT[C/G]AGGGTCTCTGTGACA | 11252 |
| rs772818715 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947247 | AGGAAGGAGGGAGAA[C/G]AGGAATGCTCCAGGC | 11252 |
| rs772828075 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006281 | TGTTTACAAGCCACC[A/G]CATCTTTGTTATAGC | 11252 |
| rs772871874 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947786 | GCCTGACAGGTTGCA[C/T]GGATCAAATGGCATC | 11252 |
| rs772875722 | snp | G/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016083 | GGTGACATGCACCTG[G/T]AATCCCAGCTTCTTG | 11252 |
| rs772897631 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954306 | CCCTTGGACAGAGAG[C/T]GGAGAACAGCCCATT | 11252 |
| rs772908590 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999409 | GCGTGGTGGCTCATG[C/T]CTCTAATCCCAGCAC | 11252 |
| rs772941747 | snp | C/G | 1.68547e-05 | 0.00290294 | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893622 | TCCCGACCTAGGAGA[C/G]AGAACCAGCTGGGAG | 11252 |
| rs772971636 | in-del | -/TT | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896407 | ATCAGAAGTTCACTC[-/TT]TCTTACTGCTAAGTA | 11252 |
| rs772973468 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918459 | ACAGATGGGTGAGGT[A/G]AACTTCAGATATATT | 11252 |
| rs773011833 | snp | A/C | 1.65627e-05 | 0.00287769 | missense | PACSIN2 | GRCh38.p7 | 22:42888798 | TCTTTGCTGCTTCTA[A/C]CTACAGGGAGAATGA | 11252 |
| rs773027705 | snp | C/T | 1.65384e-05 | 0.00287557 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884424 | GTGCTTCTGAACCTC[C/T]AGCAGAACCTCCCGG | 11252 |
| rs773031489 | snp | G/T | 0.000140499 | 0.00838031 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909552 | CGACCACAGCACTGC[G/T]GAGTTGATACCAGCT | 11252 |
| rs773047176 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967488 | CCCCAGAATCAATGA[A/C]AAGCCTTAAACTAAA | 11252 |
| rs773057987 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42957199 | GAGGGAAGACAGTTC[C/T]GACACACTGCATAAA | 11252 |
| rs773100006 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944611 | GACAAAATGTTCATC[A/G]CTGCAATATTTATAA | 11252 |
| rs773101915 | snp | A/G | 8.27959e-05 | 0.00643359 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888724 | GGATGGGTCTGCCTT[A/G]CTGTTGGCTTCTCGT | 11252 |
| rs773123036 | snp | A/G | 1.65814e-05 | 0.00287931 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877042 | CTTTCAGGGGATCCC[A/G]GCTCTGCAGGGGCCC | 11252 |
| rs773138620 | in-del | -/CGGGGCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962779 | AAGGTGTGGGCGGGG[-/CGGGGCT]GGGGGGGGCGGCGCA | 11252 |
| rs773141432 | snp | C/G | 1.69533e-05 | 0.00291142 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879041 | GATGGAGGTGGCGCC[C/G]ACTCACCTGCTGGGC | 11252 |
| rs773143634 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874120 | AAATTGAAGATGTGA[A/C]AAGCCATTTTGGTAA | 11252 |
| rs773182193 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976308 | AATTCCTGGTTCCTA[C/T]AGAGCAAGGCCAGAA | 11252 |
| rs773248747 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986395 | AGGGCAGCATTCATC[C/T]GGCCAAACGAAATCA | 11252 |
| rs773260732 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927786 | GAGATGGGGTTTCGC[C/T]ATGTTGGTCAGGCTG | 11252 |
| rs773265129 | snp | C/G/T | 1.65597e-05 | 0.00287743 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888748 | TTCTCGTGAGATAGC[C/G/T]AGCTTCTCCTCTTTG | 11252 |
| rs773281184 | snp | A/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42897260 | TTTTAATATATTTTT[A/T]AAAAAATCAAACGTA | 11252 |
| rs773330027 | snp | C/T | 1.65751e-05 | 0.00287876 | missense | PACSIN2 | GRCh38.p7 | 22:42882228 | CCGGCCCGTGATTGG[C/T]TCGGAACCACCTCAG | 11252 |
| rs773334977 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992686 | TCACGACATAGCATC[-/T]TCATTTGTGATTACA | 11252 |
| rs773353976 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960115 | CAAAATTCATACTAC[C/T]CCCTCCCCAACACAC | 11252 |
| rs773362745 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010106 | AACTCCTGACCTGAA[G/T]TGATCTGCTCCTTTA | 11252 |
| rs773402976 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907676 | GGTGGTATTGACATT[C/T]GCTCGCTTCGTGCTT | 11252 |
| rs773404608 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977541 | TACCATTTTCAGCCA[C/T]GAGATTAGCAAAAAC | 11252 |
| rs773418064 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905647 | GGGAATGGCTGAGCA[C/T]GCAGGCCGAAGACAA | 11252 |
| rs773422206 | snp | A/G | 1.73351e-05 | 0.00294402 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882322 | AAATCAGAGAGAAAC[A/G]TGGCTCTTTTAGAAG | 11252 |
| rs773468904 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904936 | CCATGGAGCTAAGCC[C/T]ACCACAGTCTAATGA | 11252 |
| rs773497372 | snp | C/T | 1.65674e-05 | 0.00287809 | missense | PACSIN2 | GRCh38.p7 | 22:42876208 | ACTCGCACTTCCGTC[C/T]CCGAGGTGGCGTCGT | 11252 |
| rs773547988 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964494 | ATAGAATACCACAGA[-/T]TTGCAGTTCTGCGCT | 11252 |
| rs773566393 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885485 | TAAGCTTTGCTGTCC[A/C]TAACAACATGTGCAG | 11252 |
| rs773567800 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984321 | GCCCTCAATGAAAAG[A/C]AACAACTATATAATT | 11252 |
| rs773567826 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996906 | TTGTCATGAGAATAA[A/G]TGTAATCACGCAAGG | 11252 |
| rs773580991 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993312 | AGTGGGGGCAGAGGG[A/C]CCCCAAGTGGCAAGA | 11252 |
| rs773586216 | snp | A/C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879713 | TGGCTTCGGAGACCT[A/C/G]AGCAAGCCTGCCATG | 11252 |
| rs773633539 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992786 | TTTTTTAAAAAATGA[A/G]ACTAACTGATAAATG | 11252 |
| rs773646268 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003110 | CGTACCTCTCTTGCC[A/T]CTTCTGAAGCTTGGT | 11252 |
| rs773658322 | snp | A/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960809 | GAAAATTCACTGATA[A/T]GTACACTTGAGATCT | 11252 |
| rs773663758 | snp | A/C | 1.65583e-05 | 0.00287731 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876907 | TGGCCTTAGTGTCGT[A/C]CTTCTCACTGACGGT | 11252 |
| rs773679698 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885443 | ATTCTTTCTACTATG[A/G]GGGTAGTCACGGGCT | 11252 |
| rs773697893 | snp | G/T | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43002411 | AAGTAGTAAGGATTT[G/T]CTAAAACAGCGTTCC | 11252 |
| rs773708973 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922999 | GGACAGGGGAGGGGT[C/G]TTTCCGGCAGAGGCA | 11252 |
| rs773715225 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948751 | TCTCAAGAAAATATT[C/G]TATTTCATTCAAAGG | 11252 |
| rs773737622 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964977 | CCTTCCTCATATGCT[A/G]CTGAAAGATGGGGAG | 11252 |
| rs773750917 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003382 | GAGGCCAAGGCAGGC[A/G]GATCACGTCAGGAGA | 11252 |
| rs773782304 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920170 | AAAAGAAACTGAGCT[C/T]CAATACCGGAATTCA | 11252 |
| rs773835629 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875864 | TTTTTTGTAGAGACA[A/G]GTTTTGCCATTTTGC | 11252 |
| rs773838990 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975050 | CTGCACTGCAGATGA[A/G]CTCTAGTCCACCACT | 11252 |
| rs773861181 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871447 | CTGCTCATCCTCGTC[C/G]TCCATCTTGGTCAGC | 11252 |
| rs773884817 | snp | A/G | 1.68057e-05 | 0.00289872 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884582 | GGAAAATCCAGGCAC[A/G]AGACAGAGGTTCATT | 11252 |
| rs773913948 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977179 | CATTTTTACAAAGAA[A/C]TAGAAATAGAAATTT | 11252 |
| rs773930772 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43000377 | CACCTGGTAACCCCA[C/T]GAGTTCCCAATGGAC | 11252 |
| rs773953090 | snp | C/T | 1.65767e-05 | 0.00287891 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911974 | AGGGCCTGCCAGACA[C/T]TATTGGCCTGGCCAC | 11252 |
| rs773968948 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917091 | ACTGCGCCCCATGCA[C/T]TACACGCGTGCACTC | 11252 |
| rs774020200 | snp | A/C | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43016865 | TATAAAAATATAGAG[A/C]CTTGTCGGGCGCTGT | 11252 |
| rs774023444 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874550 | CCTGAGACAAGGCCC[C/T]ACCTGGCCCAGGGGC | 11252 |
| rs774029293 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926643 | TTGTTTCACTCAACA[G/T]GACAGACCAAGCCCT | 11252 |
| rs774039894 | snp | G/T | 1.64844e-05 | 0.00287087 | missense | PACSIN2 | GRCh38.p7 | 22:42884504 | GCTCCATGTTCTCCA[G/T]GTACTGGGGTGTGCC | 11252 |
| rs774040998 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909221 | ATGATGACCTGCCTA[A/G]TGTCTACCTTATTCC | 11252 |
| rs774060231 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895488 | TGTATTTTGGCTCTC[C/T]TGAAACCTGCTTATC | 11252 |
| rs774076482 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883507 | TCTGCCCTGGTGAAG[C/G]CATCACAGAACCAAA | 11252 |
| rs774123427 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947861 | AAGCATTGGCCAGGG[A/C]GAAGGTGACTGGGGC | 11252 |
| rs774131303 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43001368 | TTGCCAAGGCAACAG[C/T]AACCTAGACATGTTT | 11252 |
| rs774152734 | snp | A/T | 1.66029e-05 | 0.00288117 | missense | PACSIN2 | GRCh38.p7 | 22:42879115 | GGGTGACGCCGTCAG[A/T]GGCCTTCTTCTTCTC | 11252 |
| rs774155692 | snp | C/T | 1.70699e-05 | 0.00292142 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876383 | CAGGGCGGCAGAGGG[C/T]GTGAGGCCCCCGCCC | 11252 |
| rs774157454 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944221 | GTGGAACCGCACCCC[A/C]AGCCATCCTACAAGG | 11252 |
| rs774169268 | snp | C/T | 1.6649e-05 | 0.00288518 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871349 | CCCGCTGGCCTGTCC[C/T]CGACTCATCACTGGA | 11252 |
| rs774189603 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890807 | TGGGCTTCTAGCCTG[A/G]GGAGTGGCTTCATCT | 11252 |
| rs774201244 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916169 | GAAGGTCTCAGTACC[C/T]CCAGGTCACAGGCCG | 11252 |
| rs774216674 | in-del | -/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994172 | GCCCTAGAGGGAAAC[-/TT]TGGGTAAAATGACAG | 11252 |
| rs774251848 | snp | C/T | 3.3389e-05 | 0.00408575 | missense | PACSIN2 | GRCh38.p7 | 22:42879060 | CACCTGCTGGGCTTA[C/T]TCGGCAGAGACTGGT | 11252 |
| rs774283443 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922472 | AGAAAGCCCCCGATA[C/T]CCCGCTCTAATCCTC | 11252 |
| rs774287031 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876699 | AGCTGTGCCCTCCCC[A/G]AGGAATGGGGGTGCC | 11252 |
| rs774293834 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936916 | CTCTGCCTCAAAAAA[-/G]AGGGGGGGGGGCAGG | 11252 |
| rs774294727 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971840 | GCAGCCCCGTCCGGG[-/A]GGGAGGTGGGGGGCA | 11252 |
| rs774319230 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006565 | CATGCCTGAAATCCC[A/G]GCACTTTGGGAGGCA | 11252 |
| rs774323566 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892088 | GGACCAGTATGGCAG[A/G]AGGGGCTGAGTCGCC | 11252 |
| rs774331310 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954352 | GGCTGTCCAGTATGG[C/T]AGCCACCAGCTATTA | 11252 |
| rs774351786 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899381 | CAACCTCTGCCTCCC[A/G]GGTTTAAGCGATTTT | 11252 |
| rs774356670 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880558 | ACCCACCCATGCGGG[C/T]CACAGACACCCTGCA | 11252 |
| rs774359901 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43003697 | AATGTGAAGACCTTT[C/T]GCAATTTTACAAAGT | 11252 |
| rs774374375 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997057 | GGAGGTTTGGCAACA[A/C]GCAGAGCCCTGGCAG | 11252 |
| rs774478414 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906981 | CTAGGAAATGCTGGA[A/G]AGCACAGAGGAAGAC | 11252 |
| rs774502982 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950318 | TGGTATCCTTTGGAG[A/G]GTCCTGGAACAATCC | 11252 |
| rs774539519 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925481 | CAAGACTCCGTCTTT[-/A]AAAAAAAAAAAAAAA | 11252 |
| rs774540080 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967255 | TGGCTGTGGCCTCCC[C/T]TCTTTGGCTGGGGCT | 11252 |
| rs774540664 | in-del | -/TGAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955276 | ACCAAGAAGGTAAAC[-/TGAA]TGAATGAATGAATGA | 11252 |
| rs774547151 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42898692 | TCCCTTCCCCATGCC[A/C]TTCCCCGAGCCCAGG | 11252 |
| rs774549499 | snp | G/T | 1.65666e-05 | 0.00287802 | missense | PACSIN2 | GRCh38.p7 | 22:42876257 | CCCCATTGGCATCCG[G/T]GGAGGAGAAGGGGTT | 11252 |
| rs774589444 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42962118 | AACATGGTGAAACCC[C/T]GTCTGTACTAAAAAA | 11252 |
| rs774676120 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940234 | CTCCTTAACTACTCA[G/T]TAATTAGGATGTCAT | 11252 |
| rs774687396 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877851 | TTCCAAGACCAGGGC[C/G]TCAGGGCACAGGCCC | 11252 |
| rs774691958 | in-del | -/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990038 | ATGTATATATATGTA[-/TA]TATATATATATATAC | 11252 |
| rs774710029 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986039 | GGAGGCTCACGCTTG[A/G]CTTTCCAAACAACGA | 11252 |
| rs774721098 | in-del | -/AGT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998063 | AACATATCCAAGGGC[-/AGT]TACCAGCCTTTAAGT | 11252 |
| rs774728239 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907386 | TTGCTCATGGTTCAG[C/G]AGATACTAGTTCAGT | 11252 |
| rs774749175 | snp | A/T | 1.65636e-05 | 0.00287776 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888810 | CTACCTACAGGGAGA[A/T]TGAGTTCCTGAATGC | 11252 |
| rs774761370 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972660 | GTGGCCAAAGGAGAA[C/T]TCCACCTCTGGGCTT | 11252 |
| rs774771054 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42978459 | GAAGAGCACAGGGCC[C/G]ACACTGCGTTGGTGG | 11252 |
| rs774781046 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968286 | TTCAAGTCTGCCACC[C/T]TTTTTTTCATAGTCC | 11252 |
| rs774791349 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951571 | GCTCCTGCATCCCCC[A/G]GTTGGGCTCCTCCAG | 11252 |
| rs774796195 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008774 | GACTGCAGAAAGCAT[C/G]TCATCTGTGAGGACA | 11252 |
| rs774811408 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940784 | ACAAATGGAAAAGAC[C/T]CAAATGTGTCTGTCA | 11252 |
| rs774818249 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966046 | ATCCTACTTGTTAGC[C/T]TTTCATATGTTTCAT | 11252 |
| rs774829389 | snp | C/G | 6.63163e-05 | 0.00575793 | missense | PACSIN2 | GRCh38.p7 | 22:42882235 | GTGATTGGCTCGGAA[C/G]CACCTCAGGTCCTCC | 11252 |
| rs774844755 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938831 | AAGAGAGGAGGTGCT[A/G]TTTGTGCTGGATCCC | 11252 |
| rs774845858 | snp | A/C/T | 6.92142e-05 | 0.00588243 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884341 | TTCAAAAGCACTTTC[A/C/T]GTTGACTTCAATGAC | 11252 |
| rs774862158 | in-del | -/CT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008602 | AGCTCAGAATGTGTA[-/CT]CTCTTTCAATAAACC | 11252 |
| rs774864113 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886993 | CACGCCCCCGCCCAA[A/C]ATGGAGAAGCCCCAT | 11252 |
| rs774873186 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955608 | AGTTCACTGGGTACA[C/T]CTAAGATTCAATTTA | 11252 |
| rs774901519 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880690 | CCGTAACAGCTGCAA[A/G]TGTGCGCAGAATGAA | 11252 |
| rs774922912 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939910 | CAGCGTGCAAGATAA[A/G]GTCCCTGACTTCTAG | 11252 |
| rs774938507 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949955 | TGCTAAGAGCTAGGG[C/G]ATGGAAATGAAAACA | 11252 |
| rs774952804 | in-del | -/CT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007672 | GTCAGACCCGCCCTC[-/CT]CTGTCGTGCAGTACT | 11252 |
| rs774989810 | snp | C/T | 1.65647e-05 | 0.00287786 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888655 | TACCTTAAGAACATC[C/T]TGCTTGCACTTTTCT | 11252 |
| rs775010045 | snp | A/G | 3.31235e-05 | 0.00406948 | synonymous-codon, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876986 | CTGCGCAGACTGGGC[A/G]GGGTTGCTCGGGACA | 11252 |
| rs775092175 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907733 | CCTAACTGCTCTCCA[A/T]ACAACGCTGGCTCTA | 11252 |
| rs775140596 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938178 | TGAAATCAATCACTC[A/T]CTCCACTGGAGATCC | 11252 |
| rs775143977 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006632 | CCAGCCTGGCCAACA[C/T]GGTAAAACCCCATCT | 11252 |
| rs775156947 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937659 | TCACTTACCACACCC[C/T]TTGCCTGGCCACAAA | 11252 |
| rs775166587 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901504 | GCACAGATCTGGCCC[G/T]GCCCCAAAATGTGTA | 11252 |
| rs775169681 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011999 | TAAATACAAAAATTA[A/G]CCAGGCGTGGTGGTG | 11252 |
| rs775176530 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928577 | TTTCACTGGGCCTGA[C/T]GGACTGATGCTCATT | 11252 |
| rs775238227 | in-del | -/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42993105 | CTTCAACCCGGGAGG[-/C]GGAGGTTGCAGTGAG | 11252 |
| rs775274854 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882389 | AGCCACAGCAGGTCC[C/T]GTGGTCTCTGCCCTC | 11252 |
| rs775275123 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992722 | TGGAAACAGCCCAAA[C/T]GTCTGTCAATAGGTG | 11252 |
| rs775284434 | snp | A/C | 3.32414e-05 | 0.00407671 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871483 | CCCTGCAAGACAAAG[A/C]GGGAGCCGTCTCCAT | 11252 |
| rs775285576 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988838 | TCACATGCATTTGGG[-/A]AAAAAATATAGAAAC | 11252 |
| rs775304475 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42972953 | AGAAATAAAAGCACA[C/T]ACCTGGATTTTCTAA | 11252 |
| rs775322804 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43010360 | CCTGGCAAACATGGC[C/G]GAATCCCATCTCTGT | 11252 |
| rs775353040 | snp | A/C | 1.65729e-05 | 0.00287857 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911992 | TTGGCCTGGCCACTT[A/C]ATTCACTGGAAGAAA | 11252 |
| rs775392103 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42998177 | TGATGAATAAAAACA[C/G]AAAGTCTTTGGTACC | 11252 |
| rs775403003 | in-del | -/AA/AAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983489 | GTGAGACTCCATCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 11252 |
| rs775404651 | snp | A/G | 1.66123e-05 | 0.00288199 | stop-gained, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871362 | CCCCGACTCATCACT[A/G]GATCGCCTCCACATA | 11252 |
| rs775416822 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963636 | GTACTCCTAGCCCTG[-/T]TTTACAGGGAAGGAA | 11252 |
| rs775423017 | snp | G/T | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871858 | CCTCCCCAGGGCCCC[G/T]GCCGCCTTGCTCCCA | 11252 |
| rs775424706 | snp | C/T | 1.65976e-05 | 0.00288072 | utr-variant-5-prime, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912083 | ATGTGACAGACATTT[C/T]TTCAAAGGCTGAGGG | 11252 |
| rs775436718 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42893085 | TATCTGACCTGCTAC[A/T]TGGCCAAGTTTAAAA | 11252 |
| rs775438146 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912796 | GACCTGTCCGCAGCC[A/G]AGATGAAACTGTCTG | 11252 |
| rs775444937 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999186 | ACACTGCTGTGGGGC[C/T]AGAGCCCAAAAGTGC | 11252 |
| rs775469861 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944531 | ACAGTTACCAACCTC[A/T]GACCCTTAAGTCCCA | 11252 |
| rs775474394 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881340 | ATTCCCATTCCACAC[A/G]TGGGAAAACTGAGTC | 11252 |
| rs775487526 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013740 | GCTCACCATCTGCAG[C/T]TGAGGTTCAAACTCT | 11252 |
| rs775572373 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888120 | ACCCTCCTCACCTCC[C/T]CCCTGATCCCACCCA | 11252 |
| rs775578425 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994435 | CAAAGACCCTCGGGC[A/G]TGCTTATGGGGACAC | 11252 |
| rs775584167 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966363 | AGTGAGACTGCATCT[-/A]AAAAAAAAAAAAAGC | 11252 |
| rs775585414 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951547 | CACACTGGCCAAAAC[A/C]CACCTCTTGCTCCTG | 11252 |
| rs775586557 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869900 | GGATTTCTGCTGGTA[A/G]GTTCTCAGGACAGAC | 11252 |
| rs775592716 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913638 | CTTAGTAAGTGCTAC[A/G]AACATAGTAAATAAT | 11252 |
| rs775607607 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899412 | CCTGCCTCGGCCTCC[A/C]GAGTAGCTGGGATGA | 11252 |
| rs775614511 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877915 | CCCACCACCCCAGAA[C/T]CAAGGAAGGGAGGCG | 11252 |
| rs775614900 | snp | A/C | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42947002 | ACATACTTCCCGACG[A/C]CGCCTCCTCTCCGTC | 11252 |
| rs775620324 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917439 | TAGTGAGATCCCATC[G/T]CTACAAAAAGTAGAA | 11252 |
| rs775631142 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935192 | GGCCTCCCAAAGTGC[C/T]GGGATTATAGGCGTG | 11252 |
| rs775633551 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925335 | AAATACAAAAATTAG[C/T]TGTGTGTGGTGGCGC | 11252 |
| rs775664132 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940349 | TACTGTCTTCATCTC[C/T]GAATCTCAGACGCTG | 11252 |
| rs775667855 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887070 | GCAAAGGCCCGAGAG[G/T]TCTCCCGGACCTTGT | 11252 |
| rs775683671 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951844 | TTCCAGCGCCAGTCT[C/T]GCTCCTTCCAATCCC | 11252 |
| rs775697143 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985775 | TGTCCTGGAAATCTG[-/A]TAAGTCTCCCAGACG | 11252 |
| rs775704739 | in-del | -/AAAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42944598 | AAAAATAGCTTGGAC[-/AAAA]AAAATGTTCATCACT | 11252 |
| rs775709610 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42956869 | TTATACTAATGTGGG[C/T]AGAAGCTAGAGGCCA | 11252 |
| rs775756862 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869870 | TTTTTGGTAAATCCG[-/T]TAGCACAGAAATGAG | 11252 |
| rs775786203 | in-del | -/CCCAGGGCCCCGG | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871846 | CTCTTCTGTCCCCTC[-/CCCAGGGCCCCGG]CCCAGGGCCCCGGCC | 11252 |
| rs775789675 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959407 | AAATACAGCTAAAGT[-/A]ATGTCAGCTACTCTA | 11252 |
| rs775790298 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969466 | GTTTAGATGCAAGTT[C/T]TTCTTCTTATGGAGG | 11252 |
| rs775791772 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941314 | TGGACATTTGGGTTG[C/T]TTGCCACTTTTCCGC | 11252 |
| rs775792643 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919657 | ATGCGCCTGTAATCT[C/T]AGCTACTCAGGAGGC | 11252 |
| rs775794255 | snp | C/T | 4.96899e-05 | 0.00498422 | missense | PACSIN2 | GRCh38.p7 | 22:42891021 | TGGTCTCCTTGAAGC[C/T]GCCCATCATCTGCTT | 11252 |
| rs775826839 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015387 | GTGGCGCAGATTACT[C/G]TCCCAAAGCCGCTCG | 11252 |
| rs775868866 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011358 | AGGGCGGCCTCCACA[A/G]AGCTGCCATTACAAT | 11252 |
| rs775884231 | snp | C/G | 1.66045e-05 | 0.00288132 | missense | PACSIN2 | GRCh38.p7 | 22:42879125 | GTCAGTGGCCTTCTT[C/G]TTCTCTCTCCGGCTG | 11252 |
| rs775888248 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889764 | GGGCTGGGGTGGACA[C/G]ATGACAGCCTCCAAC | 11252 |
| rs775896010 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009962 | GCAGCCTCTGCCTCC[A/C]GGGTTCTAGTGATTC | 11252 |
| rs775910382 | in-del | -/TGAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955279 | AGAAGGTAAACTGAA[-/TGAA]TGAATGAATGAATGA | 11252 |
| rs775961100 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918323 | TATTGCCTGGAGTCT[C/G]CCATGTTTGCATCAA | 11252 |
| rs775962311 | snp | A/G | 0.000894173 | 0.0211255 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42876219 | CGTCCCCGAGGTGGC[A/G]TCGTCGTCGAATGGA | 11252 |
| rs775966700 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42959454 | AGGTGCAAAGTTATT[C/G]CATCTATTTTGAAAG | 11252 |
| rs775999233 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878556 | GAAATAACCAATGCT[C/G]CTAGTGAAGAGGTAA | 11252 |
| rs776035127 | snp | C/T | 1.6773e-05 | 0.0028959 | missense, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893610 | TCCGCTTGTAGTTCC[C/T]GACCTAGGAGAGAGA | 11252 |
| rs776048389 | snp | C/G | 1.65737e-05 | 0.00287864 | missense | PACSIN2 | GRCh38.p7 | 22:42884408 | CATTGGACAGGTCTA[C/G]GTGCTTCTGAACCTC | 11252 |
| rs776050107 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881543 | AAGCCTCAGGGGCAC[C/G]AGGACCTTTGCCCAC | 11252 |
| rs776050125 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894327 | CTCACTGCAACCTCC[A/G]CATCCCAGGTTCAAG | 11252 |
| rs776064256 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999340 | CATATAAATGTCTAA[C/T]GTGTGTGTGTATGTG | 11252 |
| rs776164420 | snp | C/G | 1.65649e-05 | 0.00287788 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42877006 | TGCTCGGGACATTAA[C/G]GGTGCTATGGAGAGA | 11252 |
| rs776179922 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008617 | ACTCTTTCAATAAAC[C/T]AAAAAAATTAGTCCA | 11252 |
| rs776214062 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917657 | GTGAACACGCACTGC[C/T]CTGCGGTGTGCCGTG | 11252 |
| rs776252524 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007213 | TCTCACACACACCTC[-/T]TTGTTCTTTTTTTTT | 11252 |
| rs776257771 | snp | C/T | 1.72507e-05 | 0.00293685 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879018 | CCACCATGGAACGGC[C/T]TCTTTTGGATGGAGG | 11252 |
| rs776299452 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995782 | GTTAAAAGAAACAGT[A/G]GCCAGGCACAGTGAC | 11252 |
| rs776325332 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936405 | GCAGAATGACCCCGG[A/C]CTTAGCACAAGACTC | 11252 |
| rs776327713 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949438 | ACAAAGACCTTCAAC[A/G]TTAAGCCTCATACAC | 11252 |
| rs776385576 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902828 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 11252 |
| rs776412388 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890041 | AGAGTCTCCCTCTGT[C/T]ACCAGGCTGGAGTGC | 11252 |
| rs776427703 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887095 | CCTTGTGCTTCTTGA[A/G]CCCAGGTGCCTCCCA | 11252 |
| rs776433028 | in-del | -/TG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908076 | GATACTTATGTTCTC[-/TG]TTCATCTCCCCAAAT | 11252 |
| rs776443473 | snp | C/T | 1.66358e-05 | 0.00288402 | missense, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893543 | GCCCGCTCATGCAGG[C/T]AGTTCATGAGGTCGC | 11252 |
| rs776446837 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925578 | TGTCAAACACAAAGC[A/C]GTTGCTTTGTAAATT | 11252 |
| rs776470813 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935271 | TCCAGCAGTGTCTGC[A/G]CCATATTCCTGATTA | 11252 |
| rs776490456 | snp | C/T | 1.71843e-05 | 0.00293119 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884611 | TTTCCATTTAGCCCT[C/T]GGCTCACCCTGCCCC | 11252 |
| rs776510568 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900454 | GCCAGGGGATACTAT[C/T]AATGTCTATTTTTAA | 11252 |
| rs776523990 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914824 | CTGGATGCAGCTGTG[A/G]TCTTGACACAGTTCT | 11252 |
| rs776548470 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987692 | GCGCACCACCACACC[C/T]GGCTAATTTTTTGTA | 11252 |
| rs776567125 | in-del | -/CTCT | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015667 | GGGCGTATGTTGCTG[-/CTCT]CTCTAATAAAATATA | 11252 |
| rs776580891 | snp | A/G | 1.65597e-05 | 0.00287743 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888700 | TTTCTTGAGCTGTTC[A/G]GGGTTGAGGGATGGG | 11252 |
| rs776581686 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984952 | AAACTAAACCCTAGA[A/G]ATGGATATATGTGGA | 11252 |
| rs776599483 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989441 | AGGTGGAGGTTGCAG[C/T]GAGCCGAGATCACAC | 11252 |
| rs776604475 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872865 | CAGATGCAGGGGCCA[C/T]AGGGCAGCAGCCACG | 11252 |
| rs776614292 | snp | G/T | 3.33934e-05 | 0.00408603 | missense | PACSIN2 | GRCh38.p7 | 22:42891159 | AGGCCATCCAGGCCT[G/T]CTCCACGGTCCCGTA | 11252 |
| rs776693360 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914717 | CTGCCTGGCCAGCCA[C/T]GGGAGCAGCTGCAGG | 11252 |
| rs776697918 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878809 | TCCCTCTCTGGATCT[C/G]TCAGCAGCTCTGGCA | 11252 |
| rs776699693 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969552 | CTGGCAACGATGACC[A/T]TTGTAACACCGGCAT | 11252 |
| rs776701925 | snp | C/T | 1.65866e-05 | 0.00287976 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882144 | GTGGGCCCAGGTCCT[C/T]TTCCAGGCTGATGAG | 11252 |
| rs776711319 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887728 | ACGCTGTCTGGTTTT[A/G]AGTCCTGTGACTCCA | 11252 |
| rs776721601 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904627 | ATCTAGTGGGGAAAC[A/G]CCAGCTGGGAAAAGC | 11252 |
| rs776724883 | in-del | -/TTCTCCCTCTCCCTCTCCCTCCACG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971093 | ACCATGATAAAAATA[-/TTCTCCCTCTCCCTCTCCCTCCACG]GTCTCCCTCTGATGC | 11252 |
| rs776748163 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954229 | GATCATGCCACTGCA[C/T]TCCAGCCTAGGCGAC | 11252 |
| rs776749089 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885598 | CTACCCTGCCCATGC[A/G]GCTCCCCTCCCAGAT | 11252 |
| rs776755921 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907874 | AAGTATCACTCCACA[C/T]GGATGATGAATATGA | 11252 |
| rs776763028 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42962485 | TTGACTTCCCTCAAC[A/G]GTCAGAACTGGGTCT | 11252 |
| rs776779578 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926491 | ACTATCCACTGCAAA[C/T]TGAAGAAAAACAGTG | 11252 |
| rs776807581 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942215 | AAAGTAATGGGATTA[C/G]AGATGTGAGCCAATG | 11252 |
| rs776840559 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879611 | CAAAGTAGACAGGAG[A/C]CAGCCTCTGAGGCAC | 11252 |
| rs776851954 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921042 | CTCAAGTGATCCACT[A/G]TGCCTGCTCCAGGGT | 11252 |
| rs776881092 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942861 | CCTCCAACTTTGTTC[G/T]CTGACTTTTCAAAAC | 11252 |
| rs776906843 | snp | C/T | 3.31411e-05 | 0.00407056 | missense | PACSIN2 | GRCh38.p7 | 22:42876284 | GGTTGTTAGACTCAT[C/T]GTCTGACCAGTCGGT | 11252 |
| rs776945637 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42960036 | GAAGAGCTCTCTTTT[C/T]AGAAAGTGGCCAAAG | 11252 |
| rs776953162 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995754 | TTTCCTCCTTGAGAA[A/G]GGCAATTTGATTGTT | 11252 |
| rs776961796 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943811 | TTTGTGATAATAAGG[-/T]TATCAGAGGAAAACA | 11252 |
| rs776974389 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011501 | TTAAAGAAACTTTTC[C/G]ATCTGTTTGATATTC | 11252 |
| rs776993512 | snp | A/C | 3.32602e-05 | 0.00407786 | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871489 | AAGACAAAGAGGGAG[A/C]CGTCTCCATGAGAGG | 11252 |
| rs777040070 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905466 | AGGCTCATTGGTGCC[A/G]CTGGCCCAGTGCCCA | 11252 |
| rs777071766 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948797 | AAGCACTCTACTGTA[A/G]AGAAGAATATGGAGC | 11252 |
| rs777077122 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991258 | CCCTCCCACCCCCAT[C/G]CACCCCAGTCATAAA | 11252 |
| rs777098312 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921975 | AACTCCTGAACTCAG[A/G]TGATCCACCTGCCTC | 11252 |
| rs777103052 | snp | A/G | 3.31356e-05 | 0.00407022 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891118 | CTCGAGGTGCAGCTC[A/G]CTCACCCTCTCTGCC | 11252 |
| rs777106511 | in-del | -/ATAATC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965940 | ATCATAAATAAATAA[-/ATAATC]ATAATCATAAATAAA | 11252 |
| rs777187400 | snp | G/T | 1.64803e-05 | 0.00287052 | missense | PACSIN2 | GRCh38.p7 | 22:42884489 | ACTGCTCAAACACCT[G/T]CTCCATGTTCTCCAT | 11252 |
| rs777194255 | snp | A/G | 8.47063e-05 | 0.00650738 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876374 | CCCTCAGCACAGGGC[A/G]GCAGAGGGTGTGAGG | 11252 |
| rs777216308 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931940 | CCATGGAAACTCAAC[A/G]TTAAAGAGAACAGAA | 11252 |
| rs777216700 | snp | C/T | 1.65594e-05 | 0.0028774 | stop-gained | PACSIN2 | GRCh38.p7 | 22:42891056 | AAGGCTTCCTTCTGC[C/T]AGTTCTTGATCTTCT | 11252 |
| rs777221991 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934903 | CTCTTTCTTTTCTTT[-/T]CTTTCTTCCTTTTTC | 11252 |
| rs777237331 | in-del | -/AATA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989867 | GGAGGGGGAAAAAAA[-/AATA]TATATATATATATAT | 11252 |
| rs777240408 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869400 | GGAGATGTTTGGAGA[C/T]GCAGATAATGTAAGT | 11252 |
| rs777260704 | snp | A/G | 1.66515e-05 | 0.00288539 | missense | PACSIN2 | GRCh38.p7 | 22:42879162 | CGATTCAGGTCTGCG[A/G]ACCACTCCTAGGCAA | 11252 |
| rs777262241 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931688 | GTAATCTTCCAGCTG[C/T]TGGCTAGGCTGAGAA | 11252 |
| rs777263363 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883704 | ATTCACCTCCAGTGG[A/T]TCTTACATATGCCAG | 11252 |
| rs777264880 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945569 | CAGAAATGGTCCCAC[C/T]ATTCATTCACCCAGC | 11252 |
| rs777273038 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895590 | TGGTACCACCCATCG[A/G]CACACACAGGAGCTG | 11252 |
| rs777295308 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879279 | GCTCTGTGCATCTGA[A/T]GTGTAGACTCAGGGC | 11252 |
| rs777302763 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42970118 | CGCTGGGAAGAGGCA[C/T]AAAGCAAGCAGAGCA | 11252 |
| rs777311402 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932662 | ATTACACAGGAGAGA[A/G]AAAAGATTAGTTACT | 11252 |
| rs777313454 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920630 | GCCCATGGTGGAGGA[C/T]GTGCTGGAAGAGAGC | 11252 |
| rs777346565 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969134 | AGCCTCTAGGCAAGT[A/G]TTACATAAATACAAC | 11252 |
| rs777388939 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42869535 | CGCCAGCCGATGCCC[A/G]CACCATGTGGAAGCC | 11252 |
| rs777391617 | snp | C/T | 9.93888e-05 | 0.00704872 | missense | PACSIN2 | GRCh38.p7 | 22:42876247 | GGATTCGAGTCCCCA[C/T]TGGCATCCGTGGAGG | 11252 |
| rs777393935 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870239 | GAGCCAGGACAAAGG[C/T]CGGTCAGAAGCCGGA | 11252 |
| rs777403812 | in-del | -/TTTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42983965 | CACAGCACTTAGCAC[-/TTTTTT]TTTTTTTTTTTTTTT | 11252 |
| rs777406102 | in-del | -/TATTTTTTTTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43009864 | TCATTTTATTTTTTC[-/TATTTTTTTTTT]TTTTTTTTTTTGAGA | 11252 |
| rs777409268 | snp | A/C | | | intron-variant, downstream-variant-500B | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896883 | AGTCTAATAATACTG[A/C]AAATCTTTTCTTATG | 11252 |
| rs777451068 | snp | C/T | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42959680 | CTAGGTGCGCTTGCA[C/T]AGAAGGTGAGAGTTC | 11252 |
| rs777455977 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984673 | GAGCAGGGTAAACCA[A/G]AAGGAAAGGAAAATG | 11252 |
| rs777462007 | snp | C/T | 1.6574e-05 | 0.00287867 | synonymous-codon, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871441 | CCAGCCCTGCTCATC[C/T]TCGTCCTCCATCTTG | 11252 |
| rs777491149 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914658 | ATAGCAGGGCTTTGG[A/G]CTCAGGTGAGTCTCA | 11252 |
| rs777502695 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977079 | GCAAATATATAAACA[C/T]ATATATGCATTAATA | 11252 |
| rs777530387 | in-del | -/TTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874852 | GCATTGGGCATCCGC[-/TTTT]TTTTTTTTTTTTTTT | 11252 |
| rs777533977 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885062 | AAAAAAGTCCTCCTT[C/T]TCTTGTCTTTCAGCC | 11252 |
| rs777542829 | snp | C/T | 3.3145e-05 | 0.0040708 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882164 | AGGCTGATGAGCTCA[C/T]GGGCACACCCTCCTC | 11252 |
| rs777549427 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905304 | CCTTTTCCTGTCTCC[A/G]CGTGTGCGATGCTCC | 11252 |
| rs777557873 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42977801 | TCTCTCTCCTGCTCT[A/G]CCATGGTAAGACACG | 11252 |
| rs777558648 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911062 | GGTGCCCACCACCAC[A/G]CCCAGCTAATTTTTT | 11252 |
| rs777559197 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912185 | AACATATAACATAGT[A/G]GTTTTTAAATTCCCA | 11252 |
| rs777579128 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936843 | CTGAACCCGCGAGAC[A/G]GAGGTTGCAGTGAGC | 11252 |
| rs777602289 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42915310 | GGCATCAGACAGGAC[A/G]TATGCTCTTAGCTGA | 11252 |
| rs777604355 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42923513 | GCTCACTGTAAGCTC[C/T]GCCTCCCGGGTTCAC | 11252 |
| rs777612980 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011138 | TCTGTCTGGGGCAGG[A/G]ACGAATGATACTTTC | 11252 |
| rs777617793 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992322 | AGTGCTGGTGATGCG[C/T]GCAAAGCACTTTGGA | 11252 |
| rs777647803 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921841 | TCTCCCGGGTTCAGG[C/T]GATTCTCCTGCCTCA | 11252 |
| rs777700560 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949249 | TTTAAATGACACATT[A/G]TATGTGAGTGCCTGA | 11252 |
| rs777745162 | snp | A/G | 1.66418e-05 | 0.00288455 | missense | PACSIN2 | GRCh38.p7 | 22:42876331 | TTCTCGTAGCTGCTC[A/G]CACTGCAAGAAAGGG | 11252 |
| rs777746655 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42945439 | AGCCCCCTGATCTGC[C/T]GTCTGGCCCAGACCC | 11252 |
| rs777764814 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990521 | ACCATCCACTCTGCA[C/G]GCCCAGGGGCAAAAC | 11252 |
| rs777770635 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906805 | GAAGATTACGCAATA[C/T]ACACCATGTCTACAT | 11252 |
| rs777771672 | snp | C/T | 1.65836e-05 | 0.0028795 | missense | PACSIN2 | GRCh38.p7 | 22:42890984 | GGCTTCTGTGCCTTC[C/T]GAAAGCCGTCCTCAG | 11252 |
| rs777781852 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884315 | AACCTGGGAGCAGCA[C/T]CTGAGTTTGCTTCAA | 11252 |
| rs777790416 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948486 | TTTAAAAAGCCACAC[C/G]AGCTGGGTGTGGTGG | 11252 |
| rs777861199 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929246 | CATGCTTCCCAAGCA[C/T]GTCCACATCACATAA | 11252 |
| rs777878783 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014115 | AATGAAATTCAACAG[A/C]AGCAGCAATCACTAC | 11252 |
| rs777892356 | snp | A/C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008332 | CTCGGCTCACTGCAA[A/C/T]CTCCGCCTCCTGGGT | 11252 |
| rs777947905 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999051 | GTGACCTGATTCTTC[C/T]TGGACGCCAGATAAT | 11252 |
| rs777962132 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985859 | CTCATCTCCAACTGA[A/C]GTGATTCTCCACCCT | 11252 |
| rs777965567 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917006 | TGTGACCTTGCCACC[A/G]GCCCTCCCTTCTTCA | 11252 |
| rs778003087 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986846 | CCCATTCTAAAAAAA[A/C]CTTCCCGAAACCTAG | 11252 |
| rs778003493 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928338 | CTGCCATCTTACACA[C/T]GCATCAGAAATGGAC | 11252 |
| rs778023363 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42963292 | GTGTGCAACCAGCCT[A/G]CTCAAACCATGTGGA | 11252 |
| rs778033548 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966670 | TTAATTTTTTTCTTA[G/T]GCATTTTATAGAATC | 11252 |
| rs778040688 | in-del | -/GTAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42940481 | CACTCCTCCTTTTAC[-/GTAA]ATTCATGGAAAGGGA | 11252 |
| rs778043734 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889327 | GAGAGGACCATACTA[-/G]GGGGGCAGGGCCATC | 11252 |
| rs778059490 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881144 | AGCAGGGCCCACACT[C/G]TCATTTGGAAAAACC | 11252 |
| rs778114457 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892702 | CCATGTCAGCATCAC[A/G]GGAAAGGACAGGCAG | 11252 |
| rs778116770 | snp | A/G | 2.02263e-05 | 0.00318006 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871323 | GCTCCTGGGCCCGCC[A/G]CCTCCGTCCCCCCGC | 11252 |
| rs778135933 | snp | C/G | 1.656e-05 | 0.00287745 | missense | PACSIN2 | GRCh38.p7 | 22:42888757 | GATAGCCAGCTTCTC[C/G]TCTTTGCACGCTGCA | 11252 |
| rs778180585 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899866 | GCATGATGCCATTTA[C/T]ATCAATTAAGAATAC | 11252 |
| rs778211318 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991996 | AAAAAAGCACAAGCC[G/T]TAAAAGAACAAATTG | 11252 |
| rs778246123 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013303 | ATAAATATCACCAGC[C/T]TAATGGCCACTTTCT | 11252 |
| rs778271323 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42886873 | CTTATGTCCAACCTC[A/G]AGCCCTGGGCCTGTT | 11252 |
| rs778278146 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934854 | CACTGAAAGAAAAAA[C/T]GGAGCCAGGGCATGG | 11252 |
| rs778284802 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907524 | TGCGCACCCTGTCCC[A/G]AGGAGCCCATGGATG | 11252 |
| rs778287965 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946505 | GGTTGCAGTGAGATC[A/G]CACCACTGCACTCCA | 11252 |
| rs778291987 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872382 | GCTGGCTCGGACCTC[A/G]TCAGGAGCAAGCAAT | 11252 |
| rs778314092 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961261 | CCTTATAACACAAAA[C/T]GAAGTAGGTTAAAAA | 11252 |
| rs778333120 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924336 | GTGTTTTGTATCTGT[G/T]CTACTGTTTTTAAAA | 11252 |
| rs778339928 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911288 | AAAATTGACTTCCTA[C/T]AGTCTCAGCTACTCA | 11252 |
| rs778352549 | in-del | -/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942508 | CTAATTTTTTTAAAC[-/G]TTTTTTTAATTAAAA | 11252 |
| rs778353152 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42966532 | GTTAAAACCCTTTAC[A/G]TAAGCTTCTTTGCTT | 11252 |
| rs778370206 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933842 | ATTCTGATTGTAAGG[A/G]ATTGTAAATGTGATG | 11252 |
| rs778377242 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42932860 | CAGCCCCCAGGACAC[C/G]CCCCTGTCCACATGC | 11252 |
| rs778384694 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43002903 | TTGAGAAAATATTTA[A/C]GTGAATCTGAATAAT | 11252 |
| rs778394647 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876981 | TGTGACTGCGCAGAC[C/T]GGGCGGGGTTGCTCG | 11252 |
| rs778397519 | snp | A/G | 6.7131e-05 | 0.00579318 | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871517 | AGGTATGACACCGAC[A/G]GTGGGCTACAGAGCC | 11252 |
| rs778420151 | snp | A/T | 1.65844e-05 | 0.00287957 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912071 | CGGAATCATCATATG[A/T]GACAGACATTTTTTC | 11252 |
| rs778420398 | in-del | -/CACACACACACACACACC/CACACACACACT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889398 | ACACACACACACACA[lengthTooLong]CTCTTAACAGATCCT | 11252 |
| rs778458787 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42906338 | CTGCTCTAATCTCAA[C/T]GTCAAAGTCTGTCCA | 11252 |
| rs778461299 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960635 | AGAATACATGCTGTA[C/T]GATTCCCTTTGGATC | 11252 |
| rs778514602 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949477 | GCGCACGCACACACA[A/C]ACACATTTTGTGATG | 11252 |
| rs778517167 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992553 | AGGAGTTCAAGATCA[A/G]TCTTGGCAACATAGG | 11252 |
| rs778589119 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996533 | CAAGACTCTGCCGCA[-/AAA]AAAAAAAAAAAAAAA | 11252 |
| rs778627285 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42933659 | ACATAGGTCCACCCA[C/T]TCAAACCCCAACGGG | 11252 |
| rs778633551 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885204 | CAGCTAGAAAACGTG[C/T]GAAATTCCTAAGACA | 11252 |
| rs778642763 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42892895 | CCCCTTCCCTGCTGG[C/G]AAGTGTGTTCTAAGC | 11252 |
| rs778653338 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951024 | AGGGAAGGTTGTCCT[A/G]AGTCTTGAATGAACA | 11252 |
| rs778706043 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955988 | TTTAAGAGTCAAAGA[G/T]AGAGTTCCAAATTGG | 11252 |
| rs778711304 | in-del | -/ATT | | | | | GRCh38.p7 | 22:42943694 | TTAAAACCACCTGAC[-/ATT]ATATATTTTGATGAA | 11252 |
| rs778746324 | snp | A/G | | | | | GRCh38.p7 | 22:43002173 | CCCCATGAGAGCAGC[A/G]TCTAGAAGCTAGAGA | 11252 |
| rs778786709 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967875 | CCTGGGCCGCAGAGC[A/G]AGACTCCATCTCAAA | 11252 |
| rs778789934 | in-del | -/TGAGACTGGCTTC | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896274 | ATGCAGCCTGGCTTT[-/TGAGACTGGCTTC]TGTCACCCACCATAA | 11252 |
| rs778796202 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908313 | GCCTTCAGAGATGCA[C/G]GCAGCGGCTCTCAGC | 11252 |
| rs778818551 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988525 | CAGCAACCTGTAGAA[G/T]TCCAGGCTTAGGGTC | 11252 |
| rs778857148 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912268 | CCTTCAGTACAGGGC[A/G]GTCTATAATATTTCC | 11252 |
| rs778898373 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42934946 | TTTGAGACAGAGTTT[C/T]GCTTTATCGCCCAGG | 11252 |
| rs778903476 | snp | C/T | | | upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43017316 | TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGCGACC | 11252 |
| rs778925525 | snp | C/G | 1.67981e-05 | 0.00289806 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879192 | ACAGGTGCCGAGGGA[C/G]AGAAACCAAAGGTTC | 11252 |
| rs778936018 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938693 | CGGTGTGTGCTACCC[A/G]TGCCTGGCTGGTGAA | 11252 |
| rs778948821 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42946603 | ATGTCCCCACAGCAA[A/G]AAGCCCCAGTTACAC | 11252 |
| rs778992479 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918959 | TTGTTTCTTCAAAAC[A/G]AGGTCAGGTAGGGCA | 11252 |
| rs778995301 | snp | A/G | 5.48421e-05 | 0.00523622 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891205 | GGGGAGAGAAGCTGC[A/G]GGTCACTCAGCGCCG | 11252 |
| rs779002052 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947501 | TCAGAGGCTCTTCCC[C/T]ACCCAACAGTCTGAT | 11252 |
| rs779007081 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42925744 | TAAACACTACTGCAC[-/AT]GTTAATCTAAACCAC | 11252 |
| rs779021477 | in-del | -/A/AA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012307 | CAGAGACTCTCTCTC[-/A/AA]AAAAAAAAAAAAAAA | 11252 |
| rs779051722 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999847 | TTAAGCTTCTCTGAG[C/T]CTATTTCCTCAACTG | 11252 |
| rs779095351 | snp | C/G | 0.000142197 | 0.00843079 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909494 | GGCCATCACTGAGCA[C/G]TCACTCCGCCACTCA | 11252 |
| rs779124792 | in-del | -/CA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914186 | TGAACCACTAGGATT[-/CA]CAGAGGCTGGACAGG | 11252 |
| rs779183985 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907677 | GTGGTATTGACATTC[A/G]CTCGCTTCGTGCTTG | 11252 |
| rs779187900 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42990831 | CCATGGAAACCACTC[-/T]ATTTGGCTCAAGAGC | 11252 |
| rs779188063 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999133 | CACTTAAGCCGTCCT[C/G]AGACAGGAGGGCTAA | 11252 |
| rs779195016 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995288 | TGGCAAGCCTTAGAA[A/G]GAAGCAGAGCTACAA | 11252 |
| rs779208413 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949156 | ATTTCTTAAATAATA[A/G]GTGCACATTTTAACT | 11252 |
| rs779234565 | snp | A/C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42930033 | CAGGAACCACATGGA[A/C/G]TTTATTTTTGTGTCC | 11252 |
| rs779237809 | in-del | -/C | 2.11707e-05 | 0.00325345 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871329 | GGCCCGCCGCCTCCG[-/C]TCCCCCCGCTGGCCT | 11252 |
| rs779238506 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924685 | CACAGTGAATGTGCT[C/T]GTCTCCTCCCTGAAA | 11252 |
| rs779243574 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986973 | GATGTAAATCACACA[C/T]ACCTACACGCACACA | 11252 |
| rs779250591 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987982 | CCCGTCTCTACTAAA[C/G]ATACAAAAATTAGCC | 11252 |
| rs779256032 | in-del | -/GT | 1.72182e-05 | 0.00293408 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884357 | GTTGACTTCAATGAC[-/GT]GTGTGTTTTAGCTCA | 11252 |
| rs779280161 | in-del | -/CTTCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42885059 | TCAAAAAAAGTCCTC[-/CTTCT]CTTGTCTTTCAGCCC | 11252 |
| rs779291925 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881223 | CTGCAGGCTATGAGG[A/C]GCCCAGGAGGTTTCT | 11252 |
| rs779302062 | in-del | -/GCTAA | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894601 | CAAAGCTTTGTCAGG[-/GCTAA]GCTGAGTTTTGACTG | 11252 |
| rs779315958 | snp | A/G | 6.68382e-05 | 0.00578054 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893602 | CTTCACAGTCCGCTT[A/G]TAGTTCCCGACCTAG | 11252 |
| rs779362645 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42900964 | CTGTGGGCGCCAGCA[A/G]GTCACAAACAGAATT | 11252 |
| rs779364248 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887887 | CACAGTGCCTGGTCA[C/T]GGTCTCTCCTTGGCC | 11252 |
| rs779365269 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42914395 | GTGCCACCACGCTCG[A/G]CTAATTTTTGTATTT | 11252 |
| rs779369388 | in-del | -/AAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968025 | TCATGATAACCTTGC[-/AAA]AAGGTGGGAGTACTG | 11252 |
| rs779390673 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42878412 | TATGAAATGACTATT[A/C]CTGAGTGTCACATGG | 11252 |
| rs779406828 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43011147 | GGCAGGGACGAATGA[C/T]ACTTTCTGGTATGTG | 11252 |
| rs779419281 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42899998 | AAATAGAGACAGGAA[C/T]GGTTATTGATGAGCG | 11252 |
| rs779524864 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961143 | TGGCAAAAGAACATA[C/T]TGCAAGGGGAAACTG | 11252 |
| rs779525601 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42951149 | AAATTCAAAAGGAAG[A/G]TAAGGCAGCACGTGG | 11252 |
| rs779528805 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42922892 | ACACAGAGAAGTAGG[A/G]CACTCTAAAAGACCT | 11252 |
| rs779548347 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875462 | GCAACCTCAATCTAC[C/T]GGGCTCAGGTGATCC | 11252 |
| rs779566994 | snp | C/T | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873335 | CCCCAACCAAAGATA[C/T]CAGAAACTGGATGAA | 11252 |
| rs779576037 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42939380 | AAAGGACAAAAATGA[C/T]ACTTTTTCAAATTTG | 11252 |
| rs779613520 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42961914 | CTCCCCACACAGCCC[A/G]TCACCAAAAAAGCAG | 11252 |
| rs779674111 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941662 | TTGGGTATCTTTTCA[C/T]GTGCTTATTGGCCAT | 11252 |
| rs779683163 | snp | C/T | 3.31203e-05 | 0.00406928 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42888781 | CGCTGCATGGTGGGC[C/T]TTCTTTGCTGCTTCT | 11252 |
| rs779728755 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42979184 | ACTGCCCAAGGCCCA[A/G]TGATGGTTCATCTGT | 11252 |
| rs779760676 | snp | C/G/T | 0.000181061 | 0.00951315 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891228 | CAGCGCCGGCCATGG[C/G/T]GGGGTCTGCTCTGCT | 11252 |
| rs779764091 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42924265 | TATCACCTCTCCTTT[C/G]TGTGGCTGCAGTCTT | 11252 |
| rs779771711 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877429 | TGTGGGAGGGGCCGG[C/T]TCCCATGGATGAGTG | 11252 |
| rs779775160 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42999955 | TCTCTAAGGGCAATG[C/G]CATCACAAGTGCAGG | 11252 |
| rs779794726 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917632 | AAAACCAACCAAACA[-/A]AAAAAAAAAGTGAAC | 11252 |
| rs779806686 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42989569 | TGGGAGGCCGAGGCG[A/G]GTGGATCACGAGGTC | 11252 |
| rs779812248 | in-del | -/TA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987027 | GACGCCTTCCCTAAC[-/TA]ACACCCCTCAGACAG | 11252 |
| rs779872998 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976862 | ACTAATTTGGCTAAC[A/G]TCAGAGAATTAGTAA | 11252 |
| rs779889079 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921304 | GTGGAGGCTGCAGTG[A/G]GCCGAGATTGTGTCA | 11252 |
| rs779927774 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958447 | ATTTTTACTTATTGG[C/T]ATAAATCTCATACCT | 11252 |
| rs779930159 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901133 | TTTAATCTGTGGCCC[C/T]GAAGGCCCAAGCACC | 11252 |
| rs779938420 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005154 | TGCGTGTTATCTTAA[C/T]ACAATTTCACACAGG | 11252 |
| rs779968982 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976039 | CTGAAACCCTACAGA[A/G]TTCACAGCATTGAGG | 11252 |
| rs779974194 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968790 | TCACCTCCTGCCTTG[A/G]GCCACGGAACCCCAA | 11252 |
| rs779991479 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948158 | TAGAAACCAGCCCAG[G/T]GCAGGGTCCCGCTGG | 11252 |
| rs780034039 | snp | C/T | 1.68269e-05 | 0.00290055 | missense | PACSIN2 | GRCh38.p7 | 22:42893480 | ACGAGCTGCCTCCAG[C/T]GCCGGGCCCACTCAG | 11252 |
| rs780061460 | in-del | -/TG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904729 | ACAGCCCCCCCATAC[-/TG]CACTCCAGTCTACCT | 11252 |
| rs780130960 | snp | C/T | 1.65329e-05 | 0.0028751 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884532 | GCCCTGGTCGAGTTC[C/T]TTCAGGGACTTCTCA | 11252 |
| rs780150702 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911693 | ATAAGCTGAGCAATT[-/A]AGTGTCTGTCTCTCC | 11252 |
| rs780152450 | snp | G/T | 0.000151828 | 0.00871155 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42882295 | CAGGTCATGGTAAAT[G/T]GCTTTGTAGCTAAAT | 11252 |
| rs780152565 | in-del | -/CAGG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42931787 | ATTATGGTTAACAAC[-/CAGG]CAGGGTATATTCACT | 11252 |
| rs780201779 | snp | C/T | 1.65589e-05 | 0.00287736 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876961 | CGAAGGGGTTGTAGC[C/T]GGACTGTGACTGCGC | 11252 |
| rs780207268 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980153 | GTATTGGGTGAAAAT[C/T]TGTAAAATCTATAAT | 11252 |
| rs780220579 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916785 | TAAGGTGATTTCCTC[A/G]CAGGCATGGAGAAGG | 11252 |
| rs780227794 | snp | C/T | | | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42891070 | CCAGTTCTTGATCTT[C/T]TCGAAGTCATCGTTC | 11252 |
| rs780253119 | in-del | -/AGAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883653 | AAGGGCCTCAAAGAA[-/AGAC]TGTCCCAGGCACGAC | 11252 |
| rs780286274 | snp | A/T | | | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873394 | TCCAAAAAAACAAAA[A/T]AACCCAACTTCTCAA | 11252 |
| rs780286354 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994342 | GGGACAACCCCAAAC[A/G]CACCCAGAAAATAAG | 11252 |
| rs780288450 | snp | A/G | 1.65682e-05 | 0.00287817 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876868 | CGCGGTGGGAGCAGA[A/G]GAAGCATTTGTTCAC | 11252 |
| rs780302511 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936674 | CCAGCACTTTGGAAG[C/G]TCCAACTGGGTGGAT | 11252 |
| rs780305948 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964229 | TGGAGACCAGCCTGG[C/G]CAACATAGTGAAACC | 11252 |
| rs780318498 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42943554 | CAGTCAAGTTCCCTT[A/C]TGTTCCTGGTTTGCT | 11252 |
| rs780335204 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42883070 | AAGCTAAAATGAGGT[C/T]ACTAGCAGGGGCCCT | 11252 |
| rs780354284 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42984772 | TTAACACAAGGAGGG[A/C]AGAAAACATCCCCAA | 11252 |
| rs780360286 | snp | C/T | 1.66239e-05 | 0.00288299 | missense | PACSIN2 | GRCh38.p7 | 22:42879151 | GGCTGAGGGTTCGAT[C/T]CAGGTCTGCGGACCA | 11252 |
| rs780406744 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905136 | TTTTATCTTCAGAAG[A/G]CAAGCTTCTTGACAG | 11252 |
| rs780408220 | snp | A/G | 3.31455e-05 | 0.00407083 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871405 | TAGGCCAACTTGCCC[A/G]TTGTCCAAGCGTCCC | 11252 |
| rs780449849 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42942444 | CTGCCTAATCCAAGG[C/T]GACAAAGACTTATGC | 11252 |
| rs780452444 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42880113 | ACCAGTTACCAGACA[A/G]CTCTGATTAAAACTT | 11252 |
| rs780460949 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42908479 | AAAGAGAAGGCCTGG[A/T]AGCAGTGCCCAGAAG | 11252 |
| rs780495095 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927434 | AAATATTTTTAGTAG[A/G]GACAGGGTTTCGCCA | 11252 |
| rs780502170 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42905366 | GAGGACGCTCAGAGA[C/T]CACTCGGGCTCGGGA | 11252 |
| rs780509464 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42879339 | TCAGGCTCCCCATGC[C/T]CCACTTATGAACCCA | 11252 |
| rs780542393 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42950460 | GCATTTTGGTTGAGG[A/T]AAGAAGGCCTGCAGC | 11252 |
| rs780549120 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954833 | AAAGTCTCAAATTTC[A/G]GAGGCATGGTAGGTG | 11252 |
| rs780578618 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891349 | TTTCAGTTCCCAAAG[C/T]TGAATTTGCTCTGCC | 11252 |
| rs780585615 | in-del | -/AAAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012148 | ACTCTGTCTCAAAAT[-/AAAT]AAATAAATACATACA | 11252 |
| rs780605275 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43005994 | GATAGGGTCTCACTA[C/T]GTTACCCAGGCTGGC | 11252 |
| rs780638889 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42954116 | AAAACTCAAAAAATT[A/T]GCCAGGCATGGTGAC | 11252 |
| rs780641095 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007318 | GCCCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 11252 |
| rs780643087 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965275 | CAGGGCCAGGGGGCA[A/G]GGTGGGGGACTGACT | 11252 |
| rs780658179 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42996656 | ACAATCACACCACTA[A/C]ACTCCAGCCTGGGTG | 11252 |
| rs780660538 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42872987 | TGGATCCAGGCTACC[A/G]AGGCTAGGATGAGGC | 11252 |
| rs780676193 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926322 | TAGGCCCTCCAGAAG[C/T]ACCCATCGGCCTGGG | 11252 |
| rs780684858 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904267 | GACACCCTACATGGC[G/T]TTCACATGCACAGCA | 11252 |
| rs780691954 | snp | A/G | 0.000140855 | 0.00839093 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42909528 | AACATCCGTCATGGA[A/G]AAGGCGGACGACCAC | 11252 |
| rs780694584 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42903515 | CTGCAATTTCCACAT[C/T]CTCATTTCTATGGGA | 11252 |
| rs780723411 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42887511 | GCCCATGTCCTCTTC[C/T]TGGAGTGCAGCCTCT | 11252 |
| rs780728247 | snp | C/T | 3.31241e-05 | 0.00406952 | missense | PACSIN2 | GRCh38.p7 | 22:42888794 | GCTTTCTTTGCTGCT[C/T]CTACCTACAGGGAGA | 11252 |
| rs780802834 | snp | C/G | 1.72317e-05 | 0.00293523 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42882315 | TGTAGCTAAATCAGA[C/G]AGAAACGTGGCTCTT | 11252 |
| rs780816372 | snp | A/T | 7.13419e-05 | 0.00597209 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890934 | GGCAGGGAAGCCTGC[A/T]GGACAGATGTACCTC | 11252 |
| rs780838692 | snp | A/G | 1.66078e-05 | 0.00288161 | missense | PACSIN2 | GRCh38.p7 | 22:42879105 | ATGCCCGTCAGGGTG[A/G]CGCCGTCAGTGGCCT | 11252 |
| rs780872047 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42968962 | AGAGTCTCCAGCTTG[C/T]AGGCAGCCTGTCATA | 11252 |
| rs780903244 | snp | C/G | | | intron-variant, downstream-variant-500B | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42873687 | GTAGATGCTGCTTCT[C/G]GGGGAGCTTCACAAA | 11252 |
| rs780923075 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42935083 | ACCGCGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 11252 |
| rs780951799 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926180 | AGTGACTTATATCTC[C/T]CTGGAACATGGTGTA | 11252 |
| rs780958891 | snp | A/G | | | intron-variant, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:42995166 | TGAGCTGAAGCAGCC[A/G]AGTTCTTCCTCTATA | 11252 |
| rs780962513 | snp | A/G | | | intron-variant, nc-transcript-variant | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42896649 | CTTCGGTGAATACCT[A/G]GGAATGGAAATGTTA | 11252 |
| rs780979722 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976165 | CACCTAGAGGGAGTA[C/T]AGAACCTTGGCACCT | 11252 |
| rs780989248 | in-del | -/AAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917118 | ACTCCATTTAGTCCT[-/AAC]AACTCTATGGGGTAG | 11252 |
| rs780993454 | snp | C/G | 1.66313e-05 | 0.00288364 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893584 | GTGGCCATCGTCGAT[C/G]CGCTTCACAGTCCGC | 11252 |
| rs780998936 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920512 | GTCACTTTTTGGAAA[A/G]AAACAAATTCAAGGG | 11252 |
| rs781073397 | snp | C/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42948289 | CTAGTTACTCCACCA[C/T]AAGAGTGACTTCTGC | 11252 |
| rs781126926 | snp | A/C | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42895324 | AAAATACCCAACAAG[A/C]AACTCAGTATCGTTG | 11252 |
| rs781132005 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42938466 | ATGACCTTAGAGGAA[A/T]GGAAGGTCAGTCACA | 11252 |
| rs781154889 | snp | C/T | 1.6775e-05 | 0.00289607 | missense | PACSIN2 | GRCh38.p7 | 22:42884386 | TCAAAGGAAACTTAC[C/T]CAGCCACATTGGACA | 11252 |
| rs781169049 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42974294 | GGCCCTTTCCCATGA[A/G]CACCAAATAGCAGGT | 11252 |
| rs781207878 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958631 | ACTGATGGGCCCGAT[G/T]AAGGTCGGACAGACA | 11252 |
| rs781237147 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919175 | CATCTGGAAGGTAAA[A/G]TTCCTGGGAAGAGAG | 11252 |
| rs781237856 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42992756 | GAACAAATTGTAGCA[C/T]GCCCATGCATTGGAT | 11252 |
| rs781246635 | snp | G/T | 3.31378e-05 | 0.00407036 | missense | PACSIN2 | GRCh38.p7 | 22:42876202 | GCCCGGACTCGCACT[G/T]CCGTCCCCGAGGTGG | 11252 |
| rs781248196 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927541 | GGCGTGAGCCACCAC[A/G]CCTGGCCCCAGTCTT | 11252 |
| rs781289887 | in-del | -/AACA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42994128 | TTGCGCCAGAATGCT[-/AACA]AAAGCCAAGAGATGT | 11252 |
| rs781291903 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967007 | TCTGGAAGTTACAAA[C/G]TAAATAATTAACTTA | 11252 |
| rs781345455 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42907210 | GTCCAGCTGGCTGTC[A/C]ACACATGCTCGTGTC | 11252 |
| rs781371269 | in-del | -/CTCT | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42893780 | AGTTAGATAATGAGC[-/CTCT]CTATTTTTATTATTA | 11252 |
| rs781392687 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42985206 | GCGGCACATGCCTGT[-/A]AATCCCAGCTACTTG | 11252 |
| rs781409994 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PACSIN2 | GRCh38.p7 | 22:43015342 | CTCCTGTCAATCAAA[C/T]GGGGAGTGCCTATTT | 11252 |
| rs781420353 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42937502 | CACCACCAAAGTCCA[A/C]CTCTGAGCCCCTGCC | 11252 |
| rs781427711 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42997932 | TTGCTGAGTTCCACC[C/T]ACGTGTCTCAGAACA | 11252 |
| rs781435301 | snp | C/G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42973266 | AAAGTATTTCCAGAA[C/G/T]AGAAGGTTCAAAATG | 11252 |
| rs781461829 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976925 | CCTGAGCTAGAAGTT[A/T]CTCCAGCCGACACAA | 11252 |
| rs781477397 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875376 | CCAGGTTATTTATTT[A/G]TTTGTTTGTTTGCGA | 11252 |
| rs781537607 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42904075 | GACACAGAAACCCAG[-/A]AATTGCAATTTTCAG | 11252 |
| rs781542051 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889558 | TGACAAAAGCTAAGA[A/C]ACAGAGAAAAGGAGA | 11252 |
| rs781545097 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42964310 | GTAATCTCAGCTACT[C/G]GAGAGGCTGAGGCAG | 11252 |
| rs781557560 | snp | C/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42960665 | CCAGCACAAGAAAAG[C/G]CGTAACTAATCTACA | 11252 |
| rs781568223 | snp | C/T | 1.65592e-05 | 0.00287738 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42876901 | ACTTTTTGGCCTTAG[C/T]GTCGTCCTTCTCACT | 11252 |
| rs781582158 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871199 | AAAGGTGCCGAGTCC[C/G]AGGCGAAATGACCAG | 11252 |
| rs781593218 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42901217 | CCCAAGCTGACCTAC[A/C]GAAGAGCTCCTGGCG | 11252 |
| rs781605823 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43006162 | TGAAGCTATAAGAAG[A/T]CAGCAATCCGCAACA | 11252 |
| rs781631350 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967997 | ATATACAATGATATA[C/T]TCAGGATATACACTC | 11252 |
| rs781675451 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955810 | AAATGTTTCTGTCTT[C/T]CAAATCAATAGATAC | 11252 |
| rs781692334 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42916904 | AGGTACTCGGAAATG[G/T]TGGTGACTGGGGCTG | 11252 |
| rs781698357 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42881111 | AAGTCCTGGGGCTGG[C/T]GCAGGGGAGTGCTCG | 11252 |
| rs781719622 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42913866 | TCCAAAAACAATCTC[-/A]AAAGTTAAGTAAATC | 11252 |
| rs781723104 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43007210 | CCCCTCTCACACACA[C/G]CTCTTGTTCTTTTTT | 11252 |
| rs781724114 | snp | C/T | 1.65792e-05 | 0.00287912 | missense, intron-variant | PACSIN2 | GRCh38.p7 | 22:42912064 | ACTCCAACGGAATCA[C/T]CATATGTGACAGACA | 11252 |
| rs781733907 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43012229 | AACTAGCCAGGCAAG[G/T]TGGCAGGCGCCTGTA | 11252 |
| rs781746033 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42890748 | ATTTAAAGAATGCAC[A/G]TAGAGCATTCAGCAT | 11252 |
| rs781763572 | snp | C/G | 1.66507e-05 | 0.00288532 | synonymous-codon | PACSIN2 | GRCh38.p7 | 22:42884559 | CTCATACTTCTCTTT[C/G]GTCTAAAGGAAAATC | 11252 |
| rs781768198 | snp | C/T | 0.000315151 | 0.012549 | intron-variant | PACSIN2 | GRCh38.p7 | 22:42888617 | CACGGTGACACTCGA[C/T]GTGTAAAAACAAGTG | 11252 |
| rs796065760 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PACSIN2, LOC107985550 | GRCh38.p7 | 22:42894930 | ATGGGCAAGGGGAGG[-/G]AAGGGGGCTGCAGCA | 11252 |
| rs796073237 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875164 | CTACTTTTTTTTTTT[-/T]TTAAGAGATGGGGTC | 11252 |
| rs796073276 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42997137 | CACACCAGGCTGGGG[G/T]TGTTTAATCACGCTC | 11252 |
| rs796120296 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42980125 | ATTATAGGTATGGCA[A/T]AACAAGTATAGAGTA | 11252 |
| rs796125276 | in-del | A/TCCTGAGCCAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42876515 | ATCCTGAGCCATCAA[A/TCCTGAGCCAT]AGGCTTTCCAGGGGC | 11252 |
| rs796134846 | in-del | -/ACACAT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42889379 | ATGGTTTTTACACAC[-/ACACAT]ACACACACACACACA | 11252 |
| rs796145060 | in-del | -/AA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926673 | TCTTCTTCCCACAGG[-/AA]AAAAAAAAAAATCAT | 11252 |
| rs796201090 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967127 | AGAAACTAGGCAGGG[-/A]ATGTGGAAGGTGGGG | 11252 |
| rs796260091 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42958795 | GTATTTTCTGGAGGA[C/T]GGAGAGAGGATGCTG | 11252 |
| rs796262142 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42911329 | GTGGGAGGATGGCTT[A/G]AGCCCAGGAGATCAA | 11252 |
| rs796275517 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42986208 | GGTAAATGATCACTA[A/T]CAAAAGAGAACTTGA | 11252 |
| rs796293159 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42947675 | AAGACCCCTGGGGGT[-/GG]GGGGGGGGGGACCTC | 11252 |
| rs796328346 | snp | A/G | | | intron-variant | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42871586 | AGGCATTCTGTGGCG[A/G]GCAGGCCGAGGGCCT | 11252 |
| rs796333868 | in-del | -/TTTTCT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42917785 | CACTGATTGGTACTC[-/TTTTCT]TTTTCTTTTTCTTTT | 11252 |
| rs796340543 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42929197 | TTATCAGGGTCTCAC[C/T]GTGAAACAAGCCACA | 11252 |
| rs796351317 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42941848 | GTGGCGCATTCTCGG[C/T]TCACTGCAACCTCTG | 11252 |
| rs796355626 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013470 | TTTTCCAGGTGAATC[A/G]AGAGAGATCCAAGTT | 11252 |
| rs796379583 | snp | G/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42912576 | TCCACCTTTACTGAC[G/T]CCGCCACTGAAGCCA | 11252 |
| rs796392080 | in-del | -/AAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42919790 | AAAAAAAAAAAAAAA[-/AAG]AAAAAAAGAAAGAAA | 11252 |
| rs796429604 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42877295 | CCCAGGGGCGGGTGA[A/C]AAGCCACAGCTGGAG | 11252 |
| rs796444276 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42955184 | TGTGAGGTCCTCAGA[A/G]ACCAGAACTCAATCC | 11252 |
| rs796457286 | in-del | -/AG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936917 | CTCTGCCTCAAAAAA[-/AG]GGGGGGGGGCAGGGG | 11252 |
| rs796459907 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42967115 | GTGCTCCGTAACAGA[-/A]ACTAGGCAGGGAATG | 11252 |
| rs796468177 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | PACSIN2, LOC101927393 | GRCh38.p7 | 22:42870121 | CAGCCCGAGACACTC[A/G]TGCTGCGGGTAAGAC | 11252 |
| rs796485895 | in-del | -/AT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42965947 | AATAAATAAATAATC[-/AT]AAATAAATTATGTGA | 11252 |
| rs796501365 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971844 | CCCCGTCCGGGAGGG[A/G]GGTGGGGGGCAGCCC | 11252 |
| rs796517720 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42891508 | CAGGTTCAAGAGATT[C/T]TCCTGCCTCAGCCTC | 11252 |
| rs796524333 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42936910 | GCAAGACTCTGCCTC[-/A]AAAAAAAGGGGGGGG | 11252 |
| rs796527128 | in-del | -/CAAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982891 | AAAAAAAAAAAAAAA[-/CAAC]AACAAGGCTAGGAGC | 11252 |
| rs796557259 | in-del | C/TT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42875164 | CTACTTTTTTTTTTT[C/TT]TAAGAGATGGGGTCT | 11252 |
| rs796569515 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43002240 | GGCAGAAAGAACCCT[A/G]CAGAGTCTTTCCAAT | 11252 |
| rs796604441 | in-del | -/AAA | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42991828 | AAAAAAAAAAAAAAA[-/AAA]CCTTCAATTCACACA | 11252 |
| rs796614323 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43008242 | CATCTGTGAGGCTCT[A/G]AAATTCAGTGGTCTT | 11252 |
| rs796617568 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928425 | GGCAGGTGAGCCTCA[C/T]ATAGCTTCTAATTTC | 11252 |
| rs796621910 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42921373 | CAAAAAAGAAAAAAG[-/A]AAAAAAAAAAAAAAG | 11252 |
| rs796629886 | snp | G/T | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:42995351 | TGCTTTTGGTGCCAG[G/T]AGGACGGCAGCTTGC | 11252 |
| rs796635002 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42976979 | CATTGCTAGAGTAAA[C/T]CTTGTTTGGTCATGA | 11252 |
| rs796648329 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982185 | AGGGGCGCCTCTGCC[C/T]GGCCGCCCCTACTGG | 11252 |
| rs796705657 | in-del | -/CC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42987493 | ACACACACACACACA[-/CC]CATGGCACCATGTTC | 11252 |
| rs796766361 | in-del | -/A | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42969904 | GAGATGCTGGCCCTT[-/A]AAAAAAAAAAAGAAA | 11252 |
| rs796766495 | in-del | -/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42988897 | AGAAATTTTTTTTTT[-/T]GTTTTTGGGAGTGAG | 11252 |
| rs796770563 | in-del | -/TC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42975621 | GTATTCTTTTTTTTT[-/TC]CCTTTTTCTAACCAG | 11252 |
| rs796789884 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42920445 | TCCCATGTAGTTCCT[C/T]TGAATTTATTTCTTT | 11252 |
| rs796819591 | in-del | -/TTAGTTATTTAG | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42927581 | TATTTATTTAGTTAT[-/TTAGTTATTTAG]TTAGTTATTTTTGAG | 11252 |
| rs796831289 | snp | A/C | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42982887 | AAAAAAAAAAAAAAA[A/C]AAACAACAACAAGGC | 11252 |
| rs796847135 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42971840 | GCAGCCCCGTCCGGG[A/G]GGGAGGTGGGGGGCA | 11252 |
| rs796854410 | snp | A/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43013380 | TGATGTAGTGGCCTC[A/G]TATCTCAACCAGCAT | 11252 |
| rs796856957 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42884146 | TGCTTGGGCCAGCAA[C/T]TGGCCGGGTCAACCA | 11252 |
| rs796869583 | snp | A/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42928511 | AATACATAAGCCTCA[A/T]TTGTGAAATTTTAGA | 11252 |
| rs796871954 | in-del | AGAGCT/CACCCCCCCCCCCCC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:43014366 | AGACACACACACACC[AGAGCT/CACCCCCCCCCCCCC]GGACACGGAGGGTGG | 11252 |
| rs796879698 | multinucleotide-polymorphism | AAA/GAC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42874871 | TTTTTTTTTTTTGAA[AAA/GAC]GAGTTTTGCTCTGTC | 11252 |
| rs796906991 | snp | C/T | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42902236 | AAGCGATGTTTGAGG[C/T]GGTAGCTGAAGACAG | 11252 |
| rs796925381 | in-del | -/TTTT | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42926061 | AGCAAAGCTGGGATG[-/TTTT]TTAAGAGCTCAACTA | 11252 |
| rs796972934 | snp | A/G | | | intron-variant, upstream-variant-2KB | PACSIN2 | GRCh38.p7 | 22:43004010 | TAGATGCCGTCTTAA[A/G]CAAAGGACACACATA | 11252 |
| rs796996551 | snp | C/G | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42918617 | CAACCCAGACCATCA[C/G]ACTCCACGCTGCCCA | 11252 |
| rs797005848 | in-del | -/TC | | | intron-variant | PACSIN2 | GRCh38.p7 | 22:42949710 | CTCACACACACTCTC[-/TC]ACACACACACACACA | 11252 |