SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13186 | snp | A/C | 0.486266 | 0.0817214 | utr-variant-3-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26668038 | TTGTTTACTCACAAT[A/C]CCTAAAATCAAATTT | 8935 |
rs169873 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26668907 | TTGTTAGTGGTAGGG[G/T]GGTATTTCTTAGGAA | 8935 |
rs190033 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26668959 | AACAAAAGTACAGTA[A/G]AAAATGTTGCCAGGC | 8935 |
rs212842 | snp | A/C | 0.430434 | 0.173042 | intron-variant | SKAP2 | GRCh38.p7 | 7:26672198 | GATTCAAATTACAAG[A/C]CAGAAAGTTATTACT | 8935 |
rs212843 | snp | C/G | 0 | 0 | intron-variant | SKAP2 | GRCh38.p7 | 7:26673786 | TTTTATTTTGTAGTT[C/G]AAATTTTAGTCCCCA | 8935 |
rs212844 | snp | C/G | 0.481932 | 0.0933148 | intron-variant | SKAP2 | GRCh38.p7 | 7:26676839 | CAGCAGGATCTGAGA[C/G]ACTTTACATAGAAAG | 8935 |
rs212845 | snp | A/G | 0.497359 | 0.0362457 | intron-variant | SKAP2 | GRCh38.p7 | 7:26677908 | GTTCTAAACAACAGC[A/G]AACCATGTTATTGAC | 8935 |
rs212846 | snp | C/T | 0.486266 | 0.0817214 | intron-variant | SKAP2 | GRCh38.p7 | 7:26681994 | ACCACTCATTCTGAG[C/T]CACTAGATGGCGTAA | 8935 |
rs212847 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | SKAP2 | GRCh38.p7 | 7:26682391 | CCCATCAATAGCCCA[A/G]AATATGTCCAAATCT | 8935 |
rs212848 | snp | A/C | 0.240765 | 0.249829 | intron-variant | SKAP2 | GRCh38.p7 | 7:26682536 | AAAGAAGACCCTGTT[A/C]GCCAGCATGTTATTA | 8935 |
rs212849 | snp | A/G | 0.47709 | 0.104548 | intron-variant | SKAP2 | GRCh38.p7 | 7:26683024 | TTTACAAATAGATCC[A/G]CATGGGCTTTATAAA | 8935 |
rs212850 | snp | G/T | 0.240765 | 0.249829 | intron-variant | SKAP2 | GRCh38.p7 | 7:26684660 | GCATTCTTCCCTAGC[G/T]CTGTAAATCCAAATG | 8935 |
rs212851 | snp | C/T | 0.498832 | 0.0241331 | intron-variant | SKAP2 | GRCh38.p7 | 7:26685770 | GCTAAACACACTAGA[C/T]GCTTTTGTTACACTA | 8935 |
rs212852 | snp | A/G | 0.4862 | 0.0819127 | intron-variant | SKAP2 | GRCh38.p7 | 7:26686365 | AGGAAGAGAAAGGAG[A/G]AGGCAGTGGGAGAGA | 8935 |
rs212853 | snp | A/G | 0.454784 | 0.1434 | intron-variant | SKAP2 | GRCh38.p7 | 7:26686701 | AGTCAGATTAAATCA[A/G]TTGGTAAATGGGTCA | 8935 |
rs212854 | snp | C/G | 0.499087 | 0.0213463 | intron-variant | SKAP2 | GRCh38.p7 | 7:26686835 | ACATGCGAGGCCCTC[C/G]CCCACAGTAACTGGC | 8935 |
rs212855 | snp | G/T | 0.453697 | 0.14494 | intron-variant | SKAP2 | GRCh38.p7 | 7:26687743 | CTCAAAAGCGCAGGT[G/T]TGCAAAAGTTAACAC | 8935 |
rs212856 | snp | C/T | 0.241053 | 0.24984 | intron-variant | SKAP2 | GRCh38.p7 | 7:26689586 | AGCCTTTTAGGCCAC[C/T]AGTGTCCTTTTCCAA | 8935 |
rs212857 | snp | A/C | 0.241053 | 0.24984 | intron-variant | SKAP2 | GRCh38.p7 | 7:26690581 | CTTTCCAACTTTCCA[A/C]ATAGCAAACTTTCCA | 8935 |
rs212858 | snp | A/T | 0.448452 | 0.152042 | intron-variant | SKAP2 | GRCh38.p7 | 7:26691250 | AGAAATAAGATAAAA[A/T]TAAATGAGAAGAGCT | 8935 |
rs213524 | snp | A/G | 0.297636 | 0.24542 | intron-variant | SKAP2 | GRCh38.p7 | 7:26860161 | GATAATTTGGATTGG[A/G]TAGCTATAAAAACTG | 8935 |
rs213525 | snp | G/T | 0.219349 | 0.248114 | intron-variant | SKAP2 | GRCh38.p7 | 7:26863503 | CTTAAAAACATATAT[G/T]TTCTACCTTGTACAG | 8935 |
rs213533 | snp | A/C | 0.207253 | 0.246318 | intron-variant | SKAP2 | GRCh38.p7 | 7:26816611 | ACTGTCAATTTTTAC[A/C]ATATAAGTATGTGTT | 8935 |
rs213534 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | SKAP2 | GRCh38.p7 | 7:26833599 | aaaacagacattaaa[A/C]caacaaagatcaaaa | 8935 |
rs213535 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | SKAP2 | GRCh38.p7 | 7:26841196 | TACTCTAGTCTCTCA[C/T]TGAAATTCCATTAAT | 8935 |
rs213536 | snp | C/T | 0.100944 | 0.200705 | intron-variant | SKAP2 | GRCh38.p7 | 7:26845078 | TTCTACATTAAGTAT[C/T]TGACTGTTGAATTCA | 8935 |
rs213537 | snp | C/G | 0.030278 | 0.119257 | intron-variant | SKAP2 | GRCh38.p7 | 7:26847563 | CCAAATCAACAATAG[C/G]CATCAGGTAAACATA | 8935 |
rs380678 | snp | C/T | | | utr-variant-5-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26857457 | ACACTTTACCCGTTT[C/T]TTTTAGAATCGAATG | 8935 |
rs380703 | snp | C/T | 0 | 0 | utr-variant-5-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26857483 | GAATGAAACCAGCCT[C/T]TTCCAGGCACAGGAG | 8935 |
rs394234 | snp | C/T | 0 | 0 | intron-variant | SKAP2 | GRCh38.p7 | 7:26856968 | TCAGTTTTATAAAAA[C/T]TCAGAAAAAAAAAAA | 8935 |
rs404082 | snp | A/C | | | intron-variant | SKAP2 | GRCh38.p7 | 7:26814558 | TTCAAACACCCTTAC[A/C]CCAGCAAAAAAAAAA | 8935 |
rs420072 | snp | A/G | 0 | 0 | utr-variant-5-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26857463 | TACCCGTTTCTTTTA[A/G]AATCGAATGAAACCA | 8935 |
rs420097 | snp | A/G | 0 | 0 | utr-variant-5-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26857498 | CTTCCAGGCACAGGA[A/G]ACTCCTAGACGTGCC | 8935 |
rs420107 | snp | A/G | 0 | 0 | utr-variant-5-prime, intron-variant | SKAP2 | GRCh38.p7 | 7:26857506 | CACAGGAGACTCCTA[A/G]ACGTGCCGGTGGCGT | 8935 |
rs471536 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809066 | tccttatgtattttg[A/G]atcttaaccccttac | 8935 |
rs474462 | snp | A/G | 0.330947 | 0.236533 | intron-variant | SKAP2 | GRCh38.p7 | 7:26851580 | atgctatccctcccc[A/G]cccccaccacccctc | 8935 |
rs475238 | snp | C/T | 0.480697 | 0.0963277 | intron-variant | SKAP2 | GRCh38.p7 | 7:26808659 | TCCAAGGCTTGTCCC[C/T]TCCTTTTTTTTTATT | 8935 |
rs476098 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | SKAP2 | GRCh38.p7 | 7:26808570 | cagtggcattaagta[C/T]attcacaatgttgag | 8935 |
rs477924 | snp | C/T | 0.227664 | 0.249 | intron-variant | SKAP2 | GRCh38.p7 | 7:26814935 | TTACACTTAACTAGA[C/T]ATTTTTGATGAAGGC | 8935 |
rs484426 | snp | C/T | 0.496616 | 0.0409947 | intron-variant | SKAP2 | GRCh38.p7 | 7:26814227 | AATTTACAACAATTA[C/T]ATCAAATTTTAATAA | 8935 |
rs490366 | snp | A/G | 0.311369 | 0.242351 | intron-variant | SKAP2 | GRCh38.p7 | 7:26812186 | ACCTAGAGCCCAAAA[A/G]AGGGAAAAGAAGTGA | 8935 |
rs496173 | snp | C/T | 0.493925 | 0.054776 | intron-variant | SKAP2 | GRCh38.p7 | 7:26843540 | TAATGCGCATTTTCA[C/T]TTTTATATTGTCACT | 8935 |
rs498561 | snp | A/G | 0.496517 | 0.0415876 | intron-variant | SKAP2 | GRCh38.p7 | 7:26817875 | cttcatatcttctgt[A/G]agttgtattcctagg | 8935 |
rs501985 | snp | A/G | 0.347914 | 0.230028 | intron-variant | SKAP2 | GRCh38.p7 | 7:26808100 | ATTACCCCTAAACCT[A/G]TGTATTATTTTATTA | 8935 |
rs503110 | snp | A/T | 0.484138 | 0.0876334 | intron-variant | SKAP2 | GRCh38.p7 | 7:26817397 | TGTTTTACTATCCAC[A/T]GAGTTTTAATAGTGT | 8935 |
rs504955 | snp | A/T | 0.480618 | 0.0965156 | intron-variant | SKAP2 | GRCh38.p7 | 7:26807712 | tgagttttgccacat[A/T]gattgactcttcctt | 8935 |
rs508710 | snp | C/G | 0.40733 | 0.194287 | intron-variant | SKAP2 | GRCh38.p7 | 7:26801119 | TCAACAAAATACAAG[C/G]AATCTGAATTCAACA | 8935 |
rs513387 | snp | C/T | 0.4231 | 0.180378 | intron-variant | SKAP2 | GRCh38.p7 | 7:26784344 | CCCCAATCATTCAGA[C/T]CTAAGTTGATGGAGC | 8935 |
rs514043 | snp | C/T | 0.251578 | 0.249995 | intron-variant | SKAP2 | GRCh38.p7 | 7:26846700 | AGCCACCGCACCCGG[C/T]CTATTTTTTAAAATA | 8935 |
rs532320 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | SKAP2 | GRCh38.p7 | 7:26807041 | caacaattcagtcac[A/G]tcttcagggcctact | 8935 |
rs534981 | snp | A/G | 0.485118 | 0.0849685 | intron-variant | SKAP2 | GRCh38.p7 | 7:26806760 | tagatttcaccttaa[A/G]ggagtgttgtaactg | 8935 |
rs550141 | snp | C/T | 0.312348 | 0.242101 | intron-variant | SKAP2 | GRCh38.p7 | 7:26819680 | GCTGTCTTTTAACAA[C/T]TGAAGGCATTGAAAA | 8935 |
rs556402 | snp | C/T | 0.480618 | 0.0965156 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809547 | gaggtgttatctcat[C/T]gtggttttaatttgc | 8935 |
rs558263 | snp | G/T | 0.229136 | 0.249128 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809318 | tcaaatgattctcct[G/T]tctcagcctcccaag | 8935 |
rs559233 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809211 | ggtcaggctggtctc[A/G]aactcctgacctcag | 8935 |
rs564260 | snp | G/T | 0.480144 | 0.097642 | intron-variant | SKAP2 | GRCh38.p7 | 7:26805887 | gagttgccacagacc[G/T]tcaacttgtagaagg | 8935 |
rs567124 | snp | A/G | 0.481009 | 0.0955756 | intron-variant | SKAP2 | GRCh38.p7 | 7:26805526 | cccgaagaaagagcc[A/G]agtagaagctatata | 8935 |
rs570840 | snp | A/C | 0.483418 | 0.0895317 | intron-variant | SKAP2 | GRCh38.p7 | 7:26822520 | agcccaaggagaggc[A/C]gagagataggggaag | 8935 |
rs580904 | snp | A/G | 0.480144 | 0.097642 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809193 | ctcctgacctcaggt[A/G]atctgcccaccttgg | 8935 |
rs586947 | snp | C/G | 0.328382 | 0.237395 | intron-variant | SKAP2 | GRCh38.p7 | 7:26853009 | CCCTGTAAGTACCCA[C/G]TTTTTTTTGTGCTCT | 8935 |
rs591895 | snp | G/T | 0.257454 | 0.249889 | intron-variant | SKAP2 | GRCh38.p7 | 7:26847493 | ACCTGCAAAGACTTC[G/T]ATAAATTAAAAAAAA | 8935 |
rs592359 | snp | C/T | 0.347032 | 0.230401 | intron-variant | SKAP2 | GRCh38.p7 | 7:26807604 | ATAGCAGTGTGAAAA[C/T]GGACTAATACAGTCT | 8935 |
rs601106 | snp | A/G | 0.494936 | 0.050064 | intron-variant | SKAP2 | GRCh38.p7 | 7:26828338 | CCTTTAACATCGTTC[A/G]TTAAAAAGAATTCTT | 8935 |
rs607099 | snp | A/G | 0.481932 | 0.0933148 | intron-variant | SKAP2 | GRCh38.p7 | 7:26808540 | aaacattatgaaaac[A/G]gtgattggtggttac | 8935 |
rs609841 | snp | A/G | 0.480064 | 0.0978296 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809212 | tgaggtcaggagttt[A/G]agaccagcctgacca | 8935 |
rs615431 | snp | C/T | 0.347032 | 0.230401 | intron-variant | SKAP2 | GRCh38.p7 | 7:26795889 | AATTAcagtggaccc[C/T]tgaacaacacaggtt | 8935 |
rs622011 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | SKAP2 | GRCh38.p7 | 7:26816120 | TAACAAATGTTTTGT[C/T]CATGTTTTTGCTTAT | 8935 |
rs627539 | snp | A/G | 0.345925 | 0.230864 | intron-variant | SKAP2 | GRCh38.p7 | 7:26802830 | aggttgcagtgagtc[A/G]agatcgcactccagc | 8935 |
rs636371 | snp | G/T | 0.346147 | 0.230772 | intron-variant | SKAP2 | GRCh38.p7 | 7:26824770 | ATAGATAATTATACA[G/T]CACAGCCATACGTAT | 8935 |
rs639221 | snp | A/G | 0.466308 | 0.125343 | intron-variant | SKAP2 | GRCh38.p7 | 7:26809791 | atcagtatgtcaagg[A/G]gatatctgcactccc | 8935 |
rs640512 | snp | C/T | 0.465578 | 0.126594 | intron-variant | SKAP2 | GRCh38.p7 | 7:26810041 | ttaatttatatgtag[C/T]gttaaaaagttgggc | 8935 |
rs641968 | snp | A/T | 0.030665 | 0.119967 | intron-variant | SKAP2 | GRCh38.p7 | 7:26778380 | AAGTACTTAGAGCAA[A/T]ATTTGACAGTGTTCT | 8935 |
rs643036 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | SKAP2 | GRCh38.p7 | 7:26837427 | ggcttctgagaaagc[C/T]tcaggaagcttacaa | 8935 |
rs648297 | snp | A/C | 0.492823 | 0.0594727 | intron-variant | SKAP2 | GRCh38.p7 | 7:26824071 | aaacaacattacatg[A/C]cagagggaaatcttt | 8935 |
rs659131 | snp | C/G | 0.251014 | 0.249998 | intron-variant | SKAP2 | GRCh38.p7 | 7:26841826 | TATGGAAGGCACTAA[C/G]AAAGTATCTAAACTT | 8935 |
rs667841 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | SKAP2 | GRCh38.p7 | 7:26811612 | CAATGGGAGATGGAG[A/G]GAAGAAACTAGTCAG | 8935 |
rs668052 | snp | C/T | 0.23031 | 0.249223 | intron-variant | SKAP2 | GRCh38.p7 | 7:26828907 | cccaagtagctggga[C/T]tacaagcgcacacca | 8935 |
rs673502 | snp | G/T | 0.347032 | 0.230401 | intron-variant | SKAP2 | GRCh38.p7 | 7:26806234 | caatgacttctaagt[G/T]ttcaaataaaaggaa | 8935 |
rs680704 | snp | C/G/T | 0.381427 | 0.239821 | intron-variant | SKAP2 | GRCh38.p7 | 7:26828413 | tgggattacaggtgt[C/G/T]agccaccgcgcccgg | 8935 |
rs687254 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | SKAP2 | GRCh38.p7 | 7:26780155 | ACCTCTCTGTGCTGA[C/T]TCCTGTAAAATGAGA | 8935 |
rs687603 | snp | A/T | 0.496348 | 0.0425753 | intron-variant | SKAP2 | GRCh38.p7 | 7:26807074 | atctcatgataaaac[A/T]tgaagggatgcaaag | 8935 |
rs688039 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | SKAP2 | GRCh38.p7 | 7:26807139 | tgcgatggaatctac[C/T]accagtaaagacact | 8935 |
rs727448 | snp | A/G | 0.241053 | 0.24984 | intron-variant | SKAP2 | GRCh38.p7 | 7:26747807 | gagaggagagggagg[A/G]gaaaggggagcggag | 8935 |
rs727449 | snp | A/G | 0.371177 | 0.218669 | intron-variant | SKAP2 | GRCh38.p7 | 7:26747958 | TTTTAATGGATGTTG[A/G]TGAACACAATTGATT | 8935 |
rs727450 | snp | C/T | 0.241053 | 0.24984 | intron-variant | SKAP2 | GRCh38.p7 | 7:26748023 | AGGATAATTGGACTC[C/T]GTGTCATATAATTCA | 8935 |
rs744611 | snp | C/T | 0.429238 | 0.174281 | intron-variant | SKAP2 | GRCh38.p7 | 7:26772221 | GGTGAAAAAACAAAG[C/T]GCTGCACACCAAAAA | 8935 |
rs744612 | snp | A/G | 0.427727 | 0.175821 | intron-variant | SKAP2 | GRCh38.p7 | 7:26772502 | ATCCTAAGCAAATTA[A/G]CACAGGAACAGAAAA | 8935 |
rs763616 | snp | A/T | 0.397994 | 0.201489 | intron-variant | SKAP2 | GRCh38.p7 | 7:26744981 | TTTTATCATCAATAA[A/T]TCATCATATTATTGG | 8935 |
rs774367 | snp | A/G | 0.484138 | 0.0876334 | intron-variant | SKAP2 | GRCh38.p7 | 7:26817968 | tcttcctatccatga[A/G]catggaatgtttttc | 8935 |
rs891874 | snp | C/T | 0.454182 | 0.144256 | intron-variant | SKAP2 | GRCh38.p7 | 7:26771572 | ATAAGTAGAAGAGTA[C/T]ATACTTACATAATTT | 8935 |
rs891875 | snp | A/G | 0.428937 | 0.17459 | intron-variant | SKAP2 | GRCh38.p7 | 7:26771687 | GCTGTTGGTTAATAA[A/G]TGTATGAACCTGACA | 8935 |
rs891876 | snp | A/G | 0.429238 | 0.174281 | intron-variant | SKAP2 | GRCh38.p7 | 7:26771890 | TTATACTGAATAACA[A/G]ACGGGTTTGGACATA | 8935 |
rs934410 | snp | C/T | 0.487432 | 0.0782705 | intron-variant | SKAP2 | GRCh38.p7 | 7:26772330 | TGATTTCCTCACCCA[C/T]GTAGTGAGCATAGTA | 8935 |
rs989250 | snp | A/G | 0.463018 | 0.130857 | intron-variant | SKAP2 | GRCh38.p7 | 7:26764336 | CTATAGAAGAAGAAG[A/G]AAACATAGATCAGGA | 8935 |
rs1023711 | snp | C/T | 0.188946 | 0.24243 | intron-variant | SKAP2 | GRCh38.p7 | 7:26763444 | taacatgataccaat[C/T]tatccatccctgatg | 8935 |
rs1023712 | snp | A/C | 0.372592 | 0.217879 | intron-variant | SKAP2 | GRCh38.p7 | 7:26763544 | actttatagataata[A/C]gtatctcacagagag | 8935 |
rs1024452 | snp | A/T | 0.176861 | 0.239062 | intron-variant | SKAP2 | GRCh38.p7 | 7:26723663 | TTCATAGTTATTTTC[A/T]TAACAAAGACCTAAG | 8935 |
rs1024453 | snp | C/T | 0.237882 | 0.249706 | intron-variant | SKAP2 | GRCh38.p7 | 7:26723383 | GAGCCTGCACCTGTG[C/T]CCCGGGAAGGAAGCC | 8935 |
rs1024454 | snp | A/G | 0.495252 | 0.0484902 | intron-variant | SKAP2 | GRCh38.p7 | 7:26723326 | TTCCCTTCTTCCCCA[A/G]TGTAACTGAGAGCTG | 8935 |
rs1030644 | snp | A/C | 0.454061 | 0.144427 | intron-variant | SKAP2 | GRCh38.p7 | 7:26761792 | gtaatcccggcaact[A/C]gggagtctgaggcac | 8935 |