SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2912 | snp | C/T | 0.35574 | 0.226537 | downstream-variant-500B, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215246 | CTTGGTGGTGGAACC[C/T]GTTCTCACTCCAGTC | 57558 |
rs9922 | snp | A/T | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215467 | AAAAAAAAGAATACA[A/T]CAGAATAAATTAATA | 57558 |
rs475153 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | KCTD21, USP35 | GRCh38.p7 | 11:78190266 | gttttgtttttgttt[G/T]gtgctttttcttttg | 57558 |
rs478283 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP35 | GRCh38.p7 | 11:78191443 | CAGCAGCGCTGGCTG[A/G/T]GAAAGGCTAAGGGGT | 57558 |
rs478476 | snp | C/G | 0 | 0 | intron-variant | USP35 | GRCh38.p7 | 11:78191501 | ATTCCGAGGATCACA[C/G]AGGTAAAAGAACACC | 57558 |
rs481240 | snp | C/G | 0.154006 | 0.230836 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78218100 | AAGGCCATGTAGCAA[C/G]TGGGGAAATACATCC | 57558 |
rs482132 | snp | C/G | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217393 | ATGAGGAGAGGTGCA[C/G]CTCTTGAAGAAATAA | 57558 |
rs484005 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210652 | AAGAGCCCAACTCAG[A/C]CTCGGGCCCCTCCCT | 57558 |
rs508199 | snp | A/C/G | 1.65743e-05 | 0.00287869 | missense, synonymous-codon, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210298 | GCCGCATGGTGCGCA[A/C/G]GTCGAAAGAGAAGCG | 57558 |
rs508861 | snp | C/G/T | 4.97286e-05 | 0.00498616 | missense, synonymous-codon, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210280 | CGAAAGAGAAGCGCA[C/G/T]CAGTGTGAGGATGAG | 57558 |
rs534974 | snp | A/G | | | intron-variant | USP35 | GRCh38.p7 | 11:78204351 | CTTATTTACAAAGGC[A/G]TATGTACAAAAGGAT | 57558 |
rs542022 | snp | C/G | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217418 | AAATAACTTCTTCCA[C/G]GATGGGACTTAGAGA | 57558 |
rs542102 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217450 | TGGCTAGGCCATTGG[G/T]CTGGTGAACTATGCA | 57558 |
rs543456 | snp | G/T | 0.00938946 | 0.0678717 | intron-variant | USP35 | GRCh38.p7 | 11:78210750 | AGGCCCCACGGCTCA[G/T]CTCACCTGTAGGTAA | 57558 |
rs547090 | snp | C/G | | | missense, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210349 | GTGGCAGGCGGAGCA[C/G]CAGGGGGATGGAGAC | 57558 |
rs561670 | snp | A/G | | | intron-variant | USP35 | GRCh38.p7 | 11:78203690 | tcaggaggctgaggc[A/G]agagaatggcgtgaa | 57558 |
rs562433 | snp | A/G | | | intron-variant | USP35 | GRCh38.p7 | 11:78203647 | agcttgcaatgagcc[A/G]agatcacgccactgc | 57558 |
rs612863 | snp | C/G/T | 1.65707e-05 | 0.00287838 | synonymous-codon, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210387 | ACTGCAGAGGTCATA[C/G/T]GCCTGGCCACGGCCA | 57558 |
rs613303 | snp | G/T | 0.00353981 | 0.0419211 | missense, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210304 | TGCGGCGCCGCATGG[G/T]GCGCAGGTCGAAAGA | 57558 |
rs677020 | snp | A/G | 0 | 0 | intron-variant | USP35 | GRCh38.p7 | 11:78191650 | cactagtccaggcaa[A/G]aagtcaaggggtctt | 57558 |
rs866901 | snp | A/G | 0.356169 | 0.226336 | downstream-variant-500B, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215263 | CATCTTGTCTTGAGG[A/G]GCTTGGTGGTGGAAC | 57558 |
rs867403 | snp | C/G | 0.000414377 | 0.0143881 | intron-variant | USP35 | GRCh38.p7 | 11:78200083 | TTGAGCTGCTGAGGC[C/G]AAGTAGAATCACAAG | 57558 |
rs867404 | snp | G/T | | | intron-variant | USP35 | GRCh38.p7 | 11:78200330 | CCCAAGAGCCCAGGG[G/T]CAGTAGGCAGGGCCC | 57558 |
rs867405 | snp | C/T | | | intron-variant | USP35 | GRCh38.p7 | 11:78200326 | AGAGCCCAGGGGCAG[C/T]AGGCAGGGCCCTTAC | 57558 |
rs901099 | snp | A/C | 0.491473 | 0.0647364 | upstream-variant-2KB, intron-variant | KCTD21, USP35 | GRCh38.p7 | 11:78190241 | CAAAACAAAACAAAA[A/C]AAAAATCTGTTCCTG | 57558 |
rs901100 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | KCTD21, USP35 | GRCh38.p7 | 11:78190150 | TGTTACTCAACCTCT[C/T]CCTGCTCCAGGTCAG | 57558 |
rs901101 | snp | A/T | 0.405255 | 0.195948 | upstream-variant-2KB, intron-variant | KCTD21, USP35 | GRCh38.p7 | 11:78189180 | GCCCCCCAAAGACAG[A/T]CACACGCCCCCAACC | 57558 |
rs901105 | snp | A/C | 0.354881 | 0.226936 | intron-variant | USP35 | GRCh38.p7 | 11:78213561 | GGACCTAGAGGAAAC[A/C]TTGAAAGGTGTTGTG | 57558 |
rs1046780 | snp | C/T | 0.457271 | 0.139781 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215723 | GACCTGGGACCACAA[C/T]GGGGTACCTGCCGAG | 57558 |
rs1055248 | snp | C/T | 0.424968 | 0.178567 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214527 | GGTGTTCATGTTCCT[C/T]GTGAAGTGTGGGCTC | 57558 |
rs1055250 | snp | C/G | 0.442655 | 0.159323 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214662 | ACTTCTAACCGAAGA[C/G]AAGACAGACACCCAT | 57558 |
rs1263533 | snp | C/G | | | intron-variant | USP35 | GRCh38.p7 | 11:78203742 | aaatacaaaaaatta[C/G]ccgggcgtagtggcg | 57558 |
rs1385602 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215305 | TAAAGTCCACTAGAA[A/G]TGCACCCCAGAACCA | 57558 |
rs1552347 | snp | C/T | 0.0437281 | 0.141251 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KCTD21, USP35 | GRCh38.p7 | 11:78187103 | TGCAAGGAGAGTTTC[C/T]ACTGCGTAAGGGAAT | 57558 |
rs1683213 | snp | C/G | 0 | 0 | intron-variant | USP35 | GRCh38.p7 | 11:78191391 | ATACCCCTCGCCATA[C/G]TGGCATGACAGCATG | 57558 |
rs1787490 | snp | A/C | 0 | 0 | intron-variant | USP35 | GRCh38.p7 | 11:78210785 | GGGACTGGACTCCCT[A/C]CACCAAGAGATCAGA | 57558 |
rs1809531 | snp | C/G | 0.495891 | 0.0451408 | upstream-variant-2KB, intron-variant | KCTD21, USP35 | GRCh38.p7 | 11:78189637 | TGGAAGGAAGGGCAC[C/G]AAGCTGACACATCAG | 57558 |
rs2013290 | snp | C/G | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime | KCTD21, USP35 | GRCh38.p7 | 11:78188779 | ACGAGGCGGGGCGCA[C/G]AGCAACTCGCTGCAA | 57558 |
rs2101309 | snp | C/G | 0 | 0 | intron-variant | USP35 | GRCh38.p7 | 11:78200292 | GGGCAGTAGGCAGGG[C/G]CCTTACCAGGGGCAG | 57558 |
rs2101310 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP35 | GRCh38.p7 | 11:78200288 | AGTAGGCAGGGCCCT[C/T]ACCAGGGGCAGCAGG | 57558 |
rs2256051 | snp | C/T | 0.409985 | 0.192106 | intron-variant | USP35 | GRCh38.p7 | 11:78209411 | CACTACATGTACATG[C/T]GGGTCCCCTTCCGGG | 57558 |
rs2256187 | snp | C/T | 0.348354 | 0.22984 | intron-variant | USP35 | GRCh38.p7 | 11:78208722 | CCATGAGGTCCTCCC[C/T]GCTTTTCTATTGTCC | 57558 |
rs2256464 | snp | G/T | 0.457737 | 0.139088 | intron-variant | USP35 | GRCh38.p7 | 11:78206259 | GACCCCACTTCCCAG[G/T]GCTGCCCAGCCCCTT | 57558 |
rs2450126 | snp | C/T | 0.361263 | 0.223876 | intron-variant | USP35 | GRCh38.p7 | 11:78205233 | TCACCTCCCCAAAAC[C/T]TGACCCTACAGTCAG | 57558 |
rs2450132 | snp | G/T | 0.441841 | 0.160303 | intron-variant, upstream-variant-2KB | USP35 | GRCh38.p7 | 11:78195340 | GTGAGAGCATGGTGG[G/T]CGTGGGGGCCTCAGG | 57558 |
rs2450133 | snp | A/C | 0.395453 | 0.203331 | downstream-variant-500B, intron-variant | USP35 | GRCh38.p7 | 11:78214713 | AAGCCTAAGCAAGAG[A/C]TTGTTCTTCCTTGGA | 57558 |
rs2450134 | snp | A/G | 0.432504 | 0.170857 | downstream-variant-500B, intron-variant | USP35 | GRCh38.p7 | 11:78214732 | TTCTTCCTTGGACTC[A/G]GGGGCTGTGATGGCC | 57558 |
rs2450135 | snp | A/G | 0.259674 | 0.249813 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78216949 | CAAGGCATGGCCCCT[A/G]CACTTCTGAGTGGCT | 57558 |
rs2450136 | snp | A/C | 0.420892 | 0.182472 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214227 | CCCACCCCTTTGTGC[A/C]AGGCTTGGATCCTGC | 57558 |
rs2450137 | snp | C/G | 0.42288 | 0.182669 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214187 | TACCGTACAGCAGTC[C/G]GAAGGAAAATAGTAC | 57558 |
rs2450138 | snp | A/G | 0.346471 | 0.230637 | utr-variant-3-prime, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78213824 | GGGGTCAGGTTGGCA[A/G]CAGGTTCACATTAGA | 57558 |
rs2450139 | snp | C/T | 0.459004 | 0.137176 | intron-variant | USP35 | GRCh38.p7 | 11:78213498 | CAGTGGCAGGATATC[C/T]GGGGTGGACACCTTC | 57558 |
rs2450140 | snp | A/G | 0.400147 | 0.19989 | intron-variant | USP35 | GRCh38.p7 | 11:78213342 | GTCATATCACACCAC[A/G]CGGGAACCTGTCCGC | 57558 |
rs2510034 | snp | C/G | 0.498547 | 0.0269177 | intron-variant | USP35 | GRCh38.p7 | 11:78192221 | AGCCATGTCCTCCCC[C/G]AGGAGAGCCTGTGTT | 57558 |
rs2510042 | snp | A/G | 0.384976 | 0.210431 | intron-variant | USP35 | GRCh38.p7 | 11:78212619 | ATACCTAGGAATACA[A/G]CTAACAAGGGAAGTG | 57558 |
rs2510044 | snp | A/G | 0.308882 | 0.242967 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78197968 | AGCGCCCTGGCCAGC[A/G]TGGTCCAGCACCTCC | 57558 |
rs2510045 | snp | G/T | 0.342452 | 0.232277 | synonymous-codon, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78209517 | CAGCTCGCCCTCTCC[G/T]CCCGAGGAGCCCCCG | 57558 |
rs2511160 | snp | A/T | 0.247621 | 0.249989 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214682 | CAGACACCCATGTTC[A/T]TAAATAAATAAAAGT | 57558 |
rs2511162 | snp | A/G | 0.474634 | 0.109726 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78216055 | GGTACTGCCCACCCC[A/G]ATCCCCCAGAAAGAA | 57558 |
rs2511165 | snp | C/G | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217148 | ATCATTACCCCACTC[C/G]TGCCTCTGACACCAA | 57558 |
rs2511176 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | USP35 | GRCh38.p7 | 11:78191779 | CCTTTCCCTGACAGT[A/G]TCTGTGTCTCCCATC | 57558 |
rs2511177 | snp | C/T | 0.464096 | 0.129085 | intron-variant | USP35 | GRCh38.p7 | 11:78211914 | ACTCTGATGATAGTT[C/T]CTTGTACTCCGCATA | 57558 |
rs2511178 | snp | C/T | 0.384785 | 0.210554 | intron-variant | USP35 | GRCh38.p7 | 11:78212174 | GCTAGCCAGTTCTTC[C/T]AGCAACATTTATTAA | 57558 |
rs2511179 | snp | C/G | 0.494855 | 0.0504572 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KCTD21, USP35 | GRCh38.p7 | 11:78187942 | AGGCGTCACTATAGC[C/G]GTTGACAGGTGAGGA | 57558 |
rs2511188 | snp | C/T | 0.413752 | 0.188906 | missense, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78209884 | CTTCCTCCCTCTCTA[C/T]CCTTTCCTCCTGACT | 57558 |
rs2511189 | snp | C/T | 0.442113 | 0.159977 | intron-variant | USP35 | GRCh38.p7 | 11:78205015 | CATTCCTAACAGTTC[C/T]TCTAGCCCTGTTCTT | 57558 |
rs2512522 | snp | C/G | 0.395087 | 0.203592 | downstream-variant-500B, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78214809 | CTCCCTGTGGCATCT[C/G]ACACGTCACTGGGGG | 57558 |
rs2512525 | snp | A/G | 0.364193 | 0.222396 | intron-variant | USP35 | GRCh38.p7 | 11:78211973 | AAAAGCAATTGCAAC[A/G]AAAGCAAACAATGAC | 57558 |
rs2512526 | snp | C/G | 0.191677 | 0.243102 | missense, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78210481 | CAGTTCCCAGAGAAG[C/G]GGCAGGGCGGGCAGC | 57558 |
rs2512527 | snp | G/T | 0.32289 | 0.239147 | synonymous-codon, nc-transcript-variant | USP35 | GRCh38.p7 | 11:78209817 | GATGTACAGGCTGGT[G/T]GGGGGGGTGTCCTCT | 57558 |
rs2512530 | snp | C/T | 0.473818 | 0.111381 | intron-variant | USP35 | GRCh38.p7 | 11:78208505 | TGTCATCTTCCCAAC[C/T]CTCCCTCACTGACCT | 57558 |
rs2512539 | snp | G/T | 0.349233 | 0.229462 | intron-variant | USP35 | GRCh38.p7 | 11:78203752 | CCTGGCTAATTTTTC[G/T]TATTTTTAGTAGAGA | 57558 |
rs2629609 | snp | C/G | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217208 | GATGGCCATCAGACA[C/G]AGACTTCAAATGCTG | 57558 |
rs2629611 | snp | A/C | | | intron-variant | USP35 | GRCh38.p7 | 11:78192460 | CCTCCCTTCCCTGGC[A/C]TGATGGGGCCAGGTG | 57558 |
rs2629614 | snp | C/G | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78216784 | GCTGCTGCGGGTACA[C/G]GGAAGGCACCAGTTA | 57558 |
rs2629615 | snp | A/T | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217647 | AGAACAGCCAACATA[A/T]AAACATTCACATCCC | 57558 |
rs2848980 | snp | C/T | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217588 | GGGTAGAATGAAACG[C/T]CTGGTCTGTCCTGTT | 57558 |
rs2848981 | snp | G/T | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217593 | GAATGAAACGTCTGG[G/T]CTGTCCTGTTGCTTC | 57558 |
rs2848982 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217672 | GATCCCCCACCCTTA[G/T]TTTAAGAGAAGGAAC | 57558 |
rs2852483 | snp | C/G | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78216492 | GGGGCCTGTGAGCCA[C/G]AGCTTTGCTTTCAAA | 57558 |
rs2852484 | snp | C/G | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78216579 | TTTTGGTAGTTACCA[C/G]AATAGGGGGCTGGAA | 57558 |
rs2852485 | snp | C/G | 0 | 0 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217182 | CCCTAAGTACTTCCT[C/G]TGCCCTCCATCAGCA | 57558 |
rs3018555 | snp | A/C | | | intron-variant, upstream-variant-2KB | KCTD21, USP35 | GRCh38.p7 | 11:78188251 | GTGCCCCACCCCCAC[A/C]TAGAGATCCCGCCTC | 57558 |
rs3018556 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | KCTD21, USP35 | GRCh38.p7 | 11:78188372 | AACAGCCCCGCCCCT[A/C]TAAGAGCTCTGCCCA | 57558 |
rs3018557 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | KCTD21, USP35 | GRCh38.p7 | 11:78188406 | CGGCTCACCTCGCTC[A/C]GAAACGCGCCCCCTC | 57558 |
rs3050609 | in-del | -/CACA | | | intron-variant | USP35 | GRCh38.p7 | 11:78191178 | ACATACACACACACA[-/CACA]GGGTGCTTTGGGGTG | 57558 |
rs3102743 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | USP35 | GRCh38.p7 | 11:78192052 | GTTTCACCGTGTTAA[C/T]GAGGACCTCATCTTT | 57558 |
rs3133324 | snp | A/G | 0.418653 | 0.184544 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KCTD21, USP35 | GRCh38.p7 | 11:78188051 | TCAGTAAAGGGAGGT[A/G]TTCTATGCATCACAG | 57558 |
rs3195744 | snp | C/T | 0.243633 | 0.249919 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214474 | AGAAGCCACCACTTG[C/T]ATCCCCCTTGTGGTT | 57558 |
rs3740677 | snp | G/T | 0.47852 | 0.101384 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78216990 | GCTCAAAGGCCTTTT[G/T]TTCCCAAGACACAAG | 57558 |
rs3758662 | snp | A/G/T | 0.0263992 | 0.111815 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215432 | CCTGTCCCACCCACC[A/G/T]GATAAATATGTTACA | 57558 |
rs3830292 | in-del | -/CAC | 0.344815 | 0.231323 | intron-variant | USP35 | GRCh38.p7 | 11:78209288 | ATCCACGTACATGCT[-/CAC]AACAGCACGCTTGCT | 57558 |
rs3832723 | in-del | -/ATTA | 0.447809 | 0.152878 | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78217139 | CCACCTTCCCTGATC[-/ATTA]CCCCACTCCTGCCTC | 57558 |
rs3834429 | in-del | -/GA | | | utr-variant-3-prime, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78215539 | TCAATTTTAAATGGT[-/GA]AACAAGACAAGAACT | 57558 |
rs3841466 | in-del | -/C | 0.422473 | 0.180978 | utr-variant-3-prime, intron-variant | USP35 | GRCh38.p7 | 11:78214497 | CTTTGCAGTAAAATC[-/C]AGGACTCTAACCACA | 57558 |
rs5792798 | in-del | -/ACAC | | | intron-variant | USP35 | GRCh38.p7 | 11:78191167 | TGTGTACACACACAT[-/ACAC]ACACACACACAGGGT | 57558 |
rs6592768 | snp | A/G | 0.127944 | 0.218179 | intron-variant, upstream-variant-2KB | USP35 | GRCh38.p7 | 11:78195999 | TCCCAAAGTGCTGGG[A/G]TTACAGGTGTGAGTC | 57558 |
rs7118754 | snp | A/G | 0.131381 | 0.220067 | intron-variant, upstream-variant-2KB | USP35 | GRCh38.p7 | 11:78195635 | GTGGACAGGGTCACC[A/G]GGGAGGTCTGGGGAG | 57558 |
rs7119895 | snp | C/G | 0.0693013 | 0.172766 | intron-variant | USP35 | GRCh38.p7 | 11:78192158 | caggcaggggctcac[C/G]caaggtcacCATGAC | 57558 |
rs10532208 | in-del | -/ACTT | | | downstream-variant-500B, intron-variant | GAB2, USP35 | GRCh38.p7 | 11:78214884 | CGTGTGGACTGACTG[-/ACTT]ACTTACCTTACTGAG | 57558 |