SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs913014 | snp | C/T | 0.420733 | 0.18262 | utr-variant-3-prime | PACSIN1 | GRCh38.p7 | 6:34533752 | TGTTGTTCTGGGGGC[C/T]GTGGGGACAAGGAAG | 29993 |
rs2282249 | snp | C/T | 0.126909 | 0.217598 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34526682 | TTTCTCAGCTGTTCC[C/T]ATTTCCCTCGCTCGC | 29993 |
rs2282250 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34527187 | GCTGCGCCGCGGGGC[A/G]GGGGGCGGGGGCGGG | 29993 |
rs2282251 | snp | C/T | 0.126564 | 0.217402 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34527273 | CCGTGCTGGATGCGG[C/T]GGGCGGGGCTGGGGA | 29993 |
rs2282252 | snp | A/G | 0.163797 | 0.234668 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34527301 | GGACGCTGGGAACCC[A/G]CGGGAGTGGTGCTCG | 29993 |
rs2296575 | snp | C/T | 0.127599 | 0.217986 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34530190 | TTCAACATGGCCCCT[C/T]CTCAACCTTGGTGAG | 29993 |
rs2395564 | snp | G/T | 0.0174175 | 0.0916809 | utr-variant-5-prime | PACSIN1 | GRCh38.p7 | 6:34466236 | CCGCTTCGCCCCGAG[G/T]CGCCGCCGATGGTCC | 29993 |
rs2395565 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34482447 | tgtagcaagtaacta[C/G]tgcattcctttttat | 29993 |
rs2395566 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34482976 | acagatgttagccac[C/T]gcgcccagccAACTC | 29993 |
rs2395567 | snp | A/G | 0.457504 | 0.139435 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34510426 | ctcttctttatcact[A/G]cctcgtttgccacct | 29993 |
rs2395568 | snp | A/G | 0.186105 | 0.241697 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34517343 | ccactctgccccacc[A/G]tggtctgctcttccc | 29993 |
rs3042080 | in-del | -/AAAAA | | | intron-variant | PACSIN1 | GRCh38.p7 | 6:34487020 | aaaaaaaaaaaaaaa[-/AAAAA]nnnnttaggtggccg | 29993 |
rs3734362 | snp | C/T | 0.126219 | 0.217206 | utr-variant-3-prime | PACSIN1 | GRCh38.p7 | 6:34534245 | AGTGTCAGGACCCTC[C/T]GTGCCCACATGAAGA | 29993 |
rs3800466 | snp | A/G | 0.127254 | 0.217792 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34525235 | CTCAGGCATCTAAAC[A/G]TATTTTGTTCCCTCC | 29993 |
rs3800467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34520256 | ACCGACAGGCTCACA[A/G]CGCCTGGCTTGGGGC | 29993 |
rs3800468 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34515482 | CCCAAATGGCCAGAG[C/T]CTAGCAGTGCCTTGA | 29993 |
rs3800469 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | PACSIN1 | GRCh38.p7 | 6:34514204 | CAAGCGCACACATGG[A/G]TGGCCCTAAGCACTC | 29993 |
rs3800470 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | PACSIN1 | GRCh38.p7 | 6:34513951 | ACACAAACTCAGTGC[A/G]GCACACACAAGCCCT | 29993 |
rs3800471 | snp | A/C | 0.190833 | 0.242898 | upstream-variant-2KB, intron-variant | PACSIN1 | GRCh38.p7 | 6:34513363 | ACTCCCCAGAGAGGG[A/C]AGATACAACAGAAAG | 29993 |
rs3800472 | snp | C/T | 0.426813 | 0.17674 | upstream-variant-2KB, intron-variant | PACSIN1 | GRCh38.p7 | 6:34513315 | AAATTAAGCAAAAGG[C/T]CCTCTTGTAATAATG | 29993 |
rs3800473 | snp | C/T | 0.308414 | 0.24308 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34469193 | AAACCAAGCAGCATC[C/T]TTCTTATCTGGTATA | 29993 |
rs3823439 | snp | A/T | 0.473266 | 0.112482 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34468418 | GAATGATTGAATGAC[A/T]GAATGTCAACTCTGG | 29993 |
rs3843523 | snp | C/T | 0.265453 | 0.249522 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34519379 | GGGTGTTCCAGGCAG[C/T]CCCCAGGGAGCCTGC | 29993 |
rs3843524 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34520676 | GCAGGCGGCATCAAC[A/G]ACACAACCATTTTTG | 29993 |
rs3846865 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34475376 | ATACTTCCtgtctca[A/G]gtctggtcttctaga | 29993 |
rs3846866 | snp | C/T | 0.434831 | 0.168337 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34476145 | TGCCCAGTATTTAGC[C/T]GCCACCACCGTGGTT | 29993 |
rs3846867 | snp | C/T | 0.499137 | 0.0207489 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34480538 | ACTCATTTTTCATCA[C/T]ATATAATAGTTTCTA | 29993 |
rs3846868 | snp | A/G | 0.443195 | 0.158668 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34483068 | ggagtgcagtggcac[A/G]atcatggctcactgc | 29993 |
rs3846869 | snp | A/C | 0.497855 | 0.0326773 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34485609 | CATATCCAGGTGGGG[A/C]CGTTGAGGAGGTGGG | 29993 |
rs3846870 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34511588 | CACTGGACATTTTCT[A/C]CCCCCGATCTTCCCC | 29993 |
rs3857562 | snp | A/G | 0.499759 | 0.0109798 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34511935 | AGGGGCATGAGGGCC[A/G]CTGCCCTGTGGTGTG | 29993 |
rs3857563 | snp | G/T | 0.44306 | 0.158832 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34512128 | CCCTGTGCCAGCGTG[G/T]GACCTGCAAGTGGGA | 29993 |
rs3889226 | snp | C/T | 0.45235 | 0.146814 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34489751 | cctaacagggggcca[C/T]gatgcctctttgggt | 29993 |
rs3904668 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34496233 | AATCTTCATAATTAC[C/T]GCAGCAATTATCCCC | 29993 |
rs3997766 | snp | A/C | 0.444533 | 0.157025 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34504358 | gtgcagtggtgcgat[A/C]taggctcactgcaac | 29993 |
rs4711393 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34475688 | ggcagctgtgagctg[C/T]tagcagccagcaccc | 29993 |
rs4711394 | snp | C/G | 0.451109 | 0.148509 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34507341 | gtctgtcttctctct[C/G]cctttaagagtcttc | 29993 |
rs4713796 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34472835 | GCAAAGTGGTGGTTG[C/T]GTAGCACTGGGGAGT | 29993 |
rs4713797 | snp | A/G | 0.465052 | 0.127485 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34490756 | GGTTTCTGGCCAGAC[A/G]TGGCGGAAACCCAAG | 29993 |
rs4713798 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34490770 | CATGGCGGAAACCCA[A/G]GCATGCCCCCCTTCT | 29993 |
rs4713799 | snp | C/T | 0.444 | 0.157683 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34498695 | caagtactctggagg[C/T]tgaggtgggaggatc | 29993 |
rs4713800 | snp | A/G | 0.435119 | 0.16802 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34498721 | ggatcacctgagccc[A/G]ggaaggtcatggctg | 29993 |
rs4713801 | snp | C/T | 0.476052 | 0.106772 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34498764 | attgcaccactgcac[C/T]ccagcctaggccaca | 29993 |
rs4713802 | snp | C/G | 0.439502 | 0.163061 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34500605 | gccttagaatttcag[C/G]aatggtaaatgagca | 29993 |
rs4713803 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34501805 | ggaggccgaggaggg[C/T]ggatcaagaggtcag | 29993 |
rs4713804 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34501859 | catggtgaaacccca[C/T]ctctactaaaaatac | 29993 |
rs4713805 | snp | A/C | 0.445196 | 0.1562 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34504230 | gcatgttttgagaag[A/C]acatcagacaatgtt | 29993 |
rs4713806 | snp | C/T | 0.454423 | 0.143914 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34506852 | ggagagggaggggca[C/T]cttgttattgctggg | 29993 |
rs4713807 | snp | C/T | 0.450985 | 0.148678 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34507162 | ttttagacctatcag[C/T]aggaagcaaagagca | 29993 |
rs4713808 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34515238 | CATCCTGAGAGGTCT[C/T]GTCAGAACCGTCAGA | 29993 |
rs6457778 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34479058 | atccattcccacagc[A/G]ctccagcaaggtggc | 29993 |
rs6457779 | snp | C/T | 0.49998 | 0.00319482 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34498515 | GTTTTAAAAGTGTCC[C/T]ggctgggcacagtgg | 29993 |
rs6457780 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34504706 | ctttcctcctcccca[A/G]tgttccaggaggatt | 29993 |
rs6457781 | snp | C/T | 0.400682 | 0.199487 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34522232 | agcgaggattcaata[C/T]cagctccgctgttta | 29993 |
rs6457782 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | PACSIN1 | GRCh38.p7 | 6:34534910 | GCCTCCTCCTGTAGC[C/T]CCTGCCTGCACCCAC | 29993 |
rs6902165 | snp | A/G | 0.499971 | 0.00379382 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34498350 | caggcacgagccacc[A/G]cgcccggcccttttg | 29993 |
rs6903168 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34468962 | GACATATTTTGCATT[C/T]GTCTCCCATTAGGAG | 29993 |
rs6903333 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34523278 | TGGCCACTGTCATTG[C/T]TGTGATAGCCTTAAA | 29993 |
rs6903947 | snp | A/G | | | intron-variant | PACSIN1 | GRCh38.p7 | 6:34493344 | cgtaggttgtttggg[A/G]gctactatgaatatg | 29993 |
rs6904220 | snp | A/G | | | intron-variant | PACSIN1 | GRCh38.p7 | 6:34493744 | CCAAGGGTCTTCAAA[A/G]CCAAATCCTGGCAGA | 29993 |
rs6914721 | snp | A/G | 0.456332 | 0.141164 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34470787 | aaatgcagcatactc[A/G]ggtaattttaaattt | 29993 |
rs6915148 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34521963 | AATCCTACTCTGCGC[C/T]GCACAGGCcccaggg | 29993 |
rs6918865 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | PACSIN1 | GRCh38.p7 | 6:34483856 | gtttctccatgttgg[C/T]caggctggtctcgaa | 29993 |
rs6919434 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34531146 | gtgtgtggcacggtt[C/T]tatgcactttccata | 29993 |
rs6926784 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34502717 | gtgatctgcccacct[C/T]ggcctcccaaagtgc | 29993 |
rs6926825 | snp | C/T | 0 | 0 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34502791 | tcttggacattttag[C/T]cccagctgagggcat | 29993 |
rs6927652 | snp | G/T | 0.441021 | 0.161279 | upstream-variant-2KB | PACSIN1 | GRCh38.p7 | 6:34465733 | CGATGGGGAGATGGG[G/T]AGAGAGGCAGGGAGC | 29993 |
rs6928912 | snp | C/T | 0 | 0 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34520782 | CCCTGGAACCGGGCC[C/T]TGAGGGCTGACCAAG | 29993 |
rs6938065 | snp | A/G | 0 | 0 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34504272 | tgtgtgtgtgtgtgt[A/G]tatatatatatatat | 29993 |
rs6938948 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34474523 | ggctagatgcagtgg[C/T]tcacacctgtaatcc | 29993 |
rs7449608 | snp | C/T | | | intron-variant | PACSIN1 | GRCh38.p7 | 6:34480613 | CATCAGGGTTTTTTT[C/T]TGATTTGTGTCTACT | 29993 |
rs7450721 | snp | C/T | | | intron-variant | PACSIN1 | GRCh38.p7 | 6:34469873 | GGGGAGACAGGACCT[C/T]TAATGCCAGGGAAGT | 29993 |
rs7454888 | snp | C/T | 0.132409 | 0.220618 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34492639 | cacccacctcagcct[C/T]ccaaagtgctgggat | 29993 |
rs7738515 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34510440 | tacctcgtttgccac[A/C]tctctctgtctggct | 29993 |
rs7742005 | snp | C/T | 0.49931 | 0.0185575 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34493381 | gcaagcattcatgtg[C/T]gtgtcttttggtggc | 29993 |
rs7742811 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34493652 | CCTGGTGGGGAACCA[A/G]TGCTCCCCAATGGGT | 29993 |
rs7743448 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34477852 | ctcctgggcttgagc[G/T]atcctcacaactcag | 29993 |
rs7745896 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34499467 | atcaaagacataaat[A/G]taagaactaaatttt | 29993 |
rs7748484 | snp | A/G | 0.448708 | 0.151707 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34487553 | caggaggttgctctc[A/G]gaatcaacaggattg | 29993 |
rs7748495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34487571 | atcaacaggattgaa[A/G]gatggaggactggac | 29993 |
rs7755392 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34506536 | tatttttgtattata[C/T]cctggacacttgggg | 29993 |
rs7755546 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34506495 | gctagaattgcaggc[A/G]tgagccattgctcat | 29993 |
rs7755620 | snp | C/T | 0.452597 | 0.146474 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34467412 | GGAATGCATGACTTA[C/T]TGAATGAGTGAATGT | 29993 |
rs7757419 | snp | A/T | 0.305436 | 0.243776 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34471792 | AGATTAGCTGGGCAG[A/T]GACAGTCAGTGTAGC | 29993 |
rs7760590 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34477398 | aaagaaatcaagaaa[A/G]aaagaagaaagaaag | 29993 |
rs7763600 | snp | A/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | PACSIN1 | GRCh38.p7 | 6:34465848 | GCAGCCCCCAGAAGA[A/G]GGAGCCAGGCAAGAC | 29993 |
rs7764733 | snp | A/C | 0.0592355 | 0.161582 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34490928 | TATGGGATTGACTCT[A/C]TTTTATCCCACTTGA | 29993 |
rs7766502 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34478626 | tcctcctgcctcggc[C/T]tcccgaagtgctggg | 29993 |
rs7767802 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | PACSIN1 | GRCh38.p7 | 6:34533729 | GAAGAAGATAGTCAC[A/G]TGTTTTTCTTCCTTG | 29993 |
rs7768481 | snp | C/T | 0.453697 | 0.14494 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34496733 | GGTGGCCCCTTCCAA[C/T]TCTGGATTCCTGGAT | 29993 |
rs7773328 | snp | A/T | 0.452227 | 0.146984 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34467385 | GGGTTTGGCACCAAG[A/T]AAATATCTTGTGGAA | 29993 |
rs7773446 | snp | A/C | 0.478104 | 0.102316 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34467355 | CATCTCTGTCATTGC[A/C]CCTGCACCAAAGCAG | 29993 |
rs7773610 | snp | A/C | 0.452597 | 0.146474 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34467403 | ATATCTTGTGGAATG[A/C]ATGACTTATTGAATG | 29993 |
rs7773901 | snp | A/G | 0.452842 | 0.146134 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34467418 | CATGACTTATTGAAT[A/G]AGTGAATGTAAACTC | 29993 |
rs9296114 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34466893 | TGCCTGTTGGAGCTG[C/T]CTCTGCCCCTTATTT | 29993 |
rs9296115 | snp | A/C | 0.4711 | 0.116682 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34466938 | GCTATGAAAAGGTTA[A/C]AGGGTCATCAGGGTG | 29993 |
rs9296116 | snp | A/G | | | intron-variant | PACSIN1 | GRCh38.p7 | 6:34468725 | CCCCAGCTTGGGCTG[A/G]GAACCCCACCCATGA | 29993 |
rs9348942 | snp | G/T | 0.431769 | 0.17164 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34477105 | ACCTCAGCCCTGAGG[G/T]CTTCCTCCAGGGGCT | 29993 |
rs9348943 | snp | A/G | 0 | 0 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34503294 | aagaaaaagaaaaag[A/G]aaaaAAAAGCCTGAT | 29993 |
rs9357179 | snp | G/T | 0.454182 | 0.144256 | intron-variant | PACSIN1 | GRCh38.p7 | 6:34506786 | tactgctcctatgtg[G/T]tctccactgacctga | 29993 |