SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs16763 | snp | A/C | 0.479663 | 0.0987666 | intron-variant | VAV2 | GRCh38.p7 | 9:133927643 | TGGCCCCACTCCAAG[A/C]GGCCCCCAGATCCTC | 7410 |
rs16767 | snp | C/T | 0.422158 | 0.181278 | intron-variant | VAV2 | GRCh38.p7 | 9:133953784 | GAAACCCAGCTCCCA[C/T]GACCCCGGCTCCCAG | 7410 |
rs16803 | snp | C/T | 0.400147 | 0.19989 | intron-variant | VAV2 | GRCh38.p7 | 9:133950235 | TGCTGGGTTTCCTCT[C/T]GAGTGCTGCTGAGGA | 7410 |
rs16819 | snp | C/T | 0.446249 | 0.154875 | intron-variant | VAV2 | GRCh38.p7 | 9:133954235 | GGGACACCAGGCACA[C/T]GCCGCTTCTCAGAAA | 7410 |
rs23149 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | VAV2 | GRCh38.p7 | 9:133924407 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7410 |
rs370641 | snp | C/T | 0.471673 | 0.115589 | intron-variant | VAV2 | GRCh38.p7 | 9:133986277 | AGCAGCGTCAGGTCA[C/T]GCAACTGTAGGGGTC | 7410 |
rs370869 | snp | C/G | 0.47802 | 0.102502 | intron-variant | VAV2 | GRCh38.p7 | 9:133984075 | ctgaggcaggagaat[C/G]gcttgaacccagaag | 7410 |
rs375871 | snp | C/T | 0.28052 | 0.24813 | intron-variant | VAV2 | GRCh38.p7 | 9:133982650 | TTGCAGGGCCCACCA[C/T]CTGGTTTTGCAGGGC | 7410 |
rs378285 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133898903 | accctggaggcggag[C/G]ttgcagtgagccgag | 7410 |
rs378732 | snp | A/G | 0.447032 | 0.153878 | intron-variant | VAV2 | GRCh38.p7 | 9:133924781 | CAGGACTAAATGACC[A/G]TGAAtattcacagga | 7410 |
rs379485 | snp | C/G | 0.422473 | 0.180978 | intron-variant | VAV2 | GRCh38.p7 | 9:133979441 | CCCCTGCCTGGGGAC[C/G]CATCTCCTCTGGGCC | 7410 |
rs379996 | snp | A/G | 0.28052 | 0.24813 | intron-variant | VAV2 | GRCh38.p7 | 9:133983756 | TGACAGGGACTGACC[A/G]GGAGTGGGACTTGAG | 7410 |
rs381017 | snp | G/T | 0.441432 | 0.160792 | intron-variant | VAV2 | GRCh38.p7 | 9:133966896 | aaaaatcagttgggc[G/T]tggtggcgggcgcct | 7410 |
rs383749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV2 | GRCh38.p7 | 9:133947194 | GAAGCATCTCTTCCG[A/C]AAACAAGCAAGCAGG | 7410 |
rs386372 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133955758 | ggaacgtgggggggg[A/C]gttggggggagtggg | 7410 |
rs400924 | snp | A/G | 0.342134 | 0.232404 | intron-variant | VAV2 | GRCh38.p7 | 9:133881082 | CAGCCTCTCTGGGAC[A/G]TGGGTGGGCCATGGC | 7410 |
rs405004 | snp | A/T | 0.337158 | 0.234315 | intron-variant | VAV2 | GRCh38.p7 | 9:133924997 | TGTTCTGGACATTTC[A/T]TATAAGTGGAATCCT | 7410 |
rs410383 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133955692 | ccccaaagctcctcc[A/C]cactcccccacactc | 7410 |
rs412472 | snp | G/T | 0.441568 | 0.160629 | intron-variant | VAV2 | GRCh38.p7 | 9:133966894 | caaaaaatcagttgg[G/T]cttggtggcgggcgc | 7410 |
rs414848 | snp | C/T | 0.417845 | 0.185278 | intron-variant | VAV2 | GRCh38.p7 | 9:133978446 | AGACGGGCTCCCCAA[C/T]CCTGGGAAGGCCACA | 7410 |
rs416060 | snp | C/T | 0.280785 | 0.248097 | intron-variant | VAV2 | GRCh38.p7 | 9:133982134 | TGCCTGGCTCACTGC[C/T]GCCATCTGCTTAGAG | 7410 |
rs419240 | snp | C/G | 0.375797 | 0.216044 | intron-variant | VAV2 | GRCh38.p7 | 9:133979511 | GTCCGAGTTCCGGAC[C/G]GCTGCGGCGTCCGCT | 7410 |
rs420897 | snp | A/G | 0.404907 | 0.196224 | intron-variant | VAV2 | GRCh38.p7 | 9:133986641 | AAAGTTATGAGTACA[A/G]CACAGGTAACttttt | 7410 |
rs421510 | snp | A/G | 0.499104 | 0.0211472 | intron-variant | VAV2 | GRCh38.p7 | 9:133985122 | TATGTGTGTGTATGT[A/G]TTTATTTATGTATGT | 7410 |
rs421771 | snp | A/C | 0.472147 | 0.114677 | intron-variant | VAV2 | GRCh38.p7 | 9:133986273 | gcgtcaggtcacgca[A/C]ctgtaggggtctagc | 7410 |
rs422999 | snp | C/T | 0.409382 | 0.192607 | intron-variant | VAV2 | GRCh38.p7 | 9:133979632 | GCAGCCAGGCACTAA[C/T]CCGGGCCCGGCCCCG | 7410 |
rs425078 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | VAV2 | GRCh38.p7 | 9:133890382 | TGGGAAGCTGCAGTC[C/T]GTGCTCACTCCTGGA | 7410 |
rs425790 | snp | A/C | 0.484701 | 0.0861117 | intron-variant | VAV2 | GRCh38.p7 | 9:133978919 | ACCGGGCACCTGAGC[A/C]GGGGGCTGGCCCCGG | 7410 |
rs425850 | snp | C/T | 0.316 | 0.241131 | intron-variant | VAV2 | GRCh38.p7 | 9:133978852 | AAGCCAAACAGCGTC[C/T]CCAGCTCCAGGCAAA | 7410 |
rs429461 | snp | C/G | 0.349452 | 0.229367 | intron-variant | VAV2 | GRCh38.p7 | 9:133986970 | GGAGGCACAAAGCCT[C/G]CGTGGCACACAGCAG | 7410 |
rs431743 | snp | C/T | 0.481627 | 0.0940692 | intron-variant | VAV2 | GRCh38.p7 | 9:133922850 | agtctgatgtagtct[C/T]atttgtctgttttcg | 7410 |
rs431791 | snp | C/T | 0.303438 | 0.244222 | intron-variant | VAV2 | GRCh38.p7 | 9:133986152 | TGGTGAAGGTGGAGT[C/T]TGCTTGATTTCACTG | 7410 |
rs433035 | snp | G/T | 0.312104 | 0.242163 | intron-variant | VAV2 | GRCh38.p7 | 9:133978920 | CCGGGCACCTGAGCC[G/T]GGGGCTGGCCCCGGT | 7410 |
rs435586 | snp | C/T | 0.406641 | 0.194842 | intron-variant | VAV2 | GRCh38.p7 | 9:133979851 | CGGCAGGCTCCCTGA[C/T]GAGGTGACAGGGCGG | 7410 |
rs435943 | snp | C/T | 0.409041 | 0.192888 | intron-variant | VAV2 | GRCh38.p7 | 9:133979664 | TCAGTGGTGGGGCTC[C/T]GGGACATGGCCGGAG | 7410 |
rs436817 | snp | C/G | 0.428937 | 0.17459 | intron-variant | VAV2 | GRCh38.p7 | 9:133966811 | ttgacctcaagtgat[C/G]tgcccgccacggcct | 7410 |
rs437062 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133952997 | GGTGTCAGTGGGGCC[A/G]TGCTCCCTCCAGGTT | 7410 |
rs438210 | snp | A/G | 0.495095 | 0.0492773 | intron-variant | VAV2 | GRCh38.p7 | 9:133970364 | ACCGAACGTGGTGCC[A/G]TCCCCCAGCCTCCGC | 7410 |
rs441533 | snp | C/T | 0.306927 | 0.243432 | intron-variant | VAV2 | GRCh38.p7 | 9:133978444 | TGGCCTTCCCAGGAT[C/T]GGGGAGCCCGTCTCC | 7410 |
rs452943 | snp | A/G | 0.477853 | 0.102875 | intron-variant | VAV2 | GRCh38.p7 | 9:133967455 | agtgctacggtaaag[A/G]tgggagtgcagatat | 7410 |
rs452999 | snp | A/G | 0.422473 | 0.180978 | intron-variant | VAV2 | GRCh38.p7 | 9:133967406 | ctttcttttgtttac[A/G]tgcctggtggtagga | 7410 |
rs453703 | snp | C/T | 0.28052 | 0.24813 | intron-variant | VAV2 | GRCh38.p7 | 9:133982904 | GCAGCACGACAGCAG[C/T]CCTGGGTGGTCTGTA | 7410 |
rs471858 | snp | C/G | 0.41441 | 0.188333 | intron-variant | VAV2 | GRCh38.p7 | 9:133937621 | CCAGGGTGCTGCAGG[C/G]AAATTCATCTCTGCT | 7410 |
rs471882 | snp | C/G | 0.432063 | 0.171327 | intron-variant | VAV2 | GRCh38.p7 | 9:133960277 | ACAGATAAGAACTTT[C/G]TGGCCCAGCTTGGTC | 7410 |
rs478393 | snp | C/T | 0.448708 | 0.151707 | intron-variant | VAV2 | GRCh38.p7 | 9:133954467 | TGCGATGTGCTGCTG[C/T]GGCACTGAGTACTTT | 7410 |
rs478403 | snp | C/T | 0.39214 | 0.205661 | intron-variant | VAV2 | GRCh38.p7 | 9:133774131 | cagatgttaaaccaa[C/T]cttgcattcctggaa | 7410 |
rs478645 | snp | C/T | 0.462144 | 0.132269 | intron-variant | VAV2 | GRCh38.p7 | 9:133925567 | GATCACCCAGGGCTC[C/T]AGCCCCAAAGTCCCC | 7410 |
rs481964 | snp | A/G | 0.432504 | 0.170857 | intron-variant | VAV2 | GRCh38.p7 | 9:133948219 | AGACAAAATCAACTC[A/G]TGACACTCCTCAATC | 7410 |
rs484440 | snp | C/G | 0.428635 | 0.174898 | intron-variant | VAV2 | GRCh38.p7 | 9:133957912 | TGTTTCAGAGAGCAC[C/G]GGGTTGGGGGTAAGG | 7410 |
rs485458 | snp | A/G | 0.433673 | 0.1696 | intron-variant | VAV2 | GRCh38.p7 | 9:133948531 | CAGGGCAGGCGGCCC[A/G]CGTGCCCTCAGGAGT | 7410 |
rs490177 | snp | C/G | 0.383439 | 0.21141 | intron-variant | VAV2 | GRCh38.p7 | 9:133958543 | acacatccccctctc[C/G]gagaaacacccacga | 7410 |
rs493433 | snp | A/G | 0.454423 | 0.143914 | intron-variant | VAV2 | GRCh38.p7 | 9:133950868 | GGTCAACATGAGGGC[A/G]TTCGCACGCTCTCTG | 7410 |
rs503376 | snp | C/G | 0.438666 | 0.164028 | intron-variant | VAV2 | GRCh38.p7 | 9:133954840 | TTAGCTTTATTTATC[C/G]TAATGCAGACACACA | 7410 |
rs503596 | snp | A/G | 0.415891 | 0.18703 | intron-variant | VAV2 | GRCh38.p7 | 9:133945402 | GGGGCTGACCTGATT[A/G]ATCGGCACATAATAA | 7410 |
rs504375 | snp | A/C | 0.5 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133926001 | CTGTGGACATGGACC[A/C]AAAAAAAAAAAAAAA | 7410 |
rs506278 | snp | C/T | 0.405603 | 0.195673 | intron-variant | VAV2 | GRCh38.p7 | 9:133773400 | ctaggccttcacatt[C/T]actcaccactctcca | 7410 |
rs508878 | snp | C/T | 0.444444 | 0.157135 | intron-variant | VAV2 | GRCh38.p7 | 9:133773134 | TGCAGTAGGCTCTGC[C/T]GTCCAGCCTAGGTGT | 7410 |
rs509590 | snp | A/G | 0.499663 | 0.0129749 | utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133763648 | AGGGGACCTGCCCCC[A/G]CACCCTCTGCTCAGC | 7410 |
rs520308 | snp | A/G | 0.429238 | 0.174281 | intron-variant | VAV2 | GRCh38.p7 | 9:133942116 | CTCAGTGTCTTCTCC[A/G]GTTTTCCTCTAGAGC | 7410 |
rs521418 | snp | A/C | 0.488241 | 0.0757703 | intron-variant | VAV2 | GRCh38.p7 | 9:133782891 | GGGTCGGGGGCATAC[A/C]TTTGGGGTTGTGCCC | 7410 |
rs524538 | snp | G/T | 0.459574 | 0.136304 | intron-variant | VAV2 | GRCh38.p7 | 9:133951976 | atctctgctgtgtaa[G/T]ggtacaaggagaagc | 7410 |
rs525060 | snp | A/G | 0.468148 | 0.122112 | intron-variant | VAV2 | GRCh38.p7 | 9:133782502 | CCCTAACCTGGGGAG[A/G]GGGCCAGAAGGTCAG | 7410 |
rs526581 | snp | A/G | 0.460252 | 0.135255 | intron-variant | VAV2 | GRCh38.p7 | 9:133952229 | ATGGGTGGGCCCCAA[A/G]GAGACAGGTCTGCAT | 7410 |
rs527316 | snp | C/G | 0.46014 | 0.13543 | intron-variant | VAV2 | GRCh38.p7 | 9:133952260 | CCAGACCCTGAGAAG[C/G]CTATTTGTGACCTTA | 7410 |
rs532646 | snp | A/C | 0.463774 | 0.129618 | intron-variant | VAV2 | GRCh38.p7 | 9:133946231 | CTCAAGGCAGCTGCC[A/C]GGGACTGGGGGAGGG | 7410 |
rs533771 | snp | C/T | 0.5 | 0.00019968 | intron-variant | VAV2 | GRCh38.p7 | 9:133766134 | ACCTTTCCCAGGGCT[C/T]CCCATTTCCTCCTGC | 7410 |
rs538287 | snp | C/T | 0.476574 | 0.105661 | intron-variant | VAV2 | GRCh38.p7 | 9:133927411 | ATGGGAGGCCACCCA[C/T]GGTCAGAGAACACAG | 7410 |
rs540626 | snp | C/G | 0.417472 | 0.185615 | intron-variant | VAV2 | GRCh38.p7 | 9:133779957 | CCTCATCTCTGTGTT[C/G]TGTCCTTGTCCTCAC | 7410 |
rs545246 | snp | A/G | 0.243919 | 0.249926 | intron-variant | VAV2 | GRCh38.p7 | 9:133779410 | CCCAGCCCAGCTCCC[A/G]CCTGGCCCAGCAGCA | 7410 |
rs556664 | snp | A/C | 0.45645 | 0.140991 | intron-variant | VAV2 | GRCh38.p7 | 9:133765902 | aaatttcaacttaaa[A/C]gtgtcagtaacctgc | 7410 |
rs557327 | snp | A/G | 0.464309 | 0.12873 | intron-variant | VAV2 | GRCh38.p7 | 9:133946650 | GTGCTGACTCCCTGG[A/G]GCCACAATGCTGCGT | 7410 |
rs557430 | snp | A/G | 0.499999 | 0.000599041 | intron-variant | VAV2 | GRCh38.p7 | 9:133765843 | cccatttgctttatc[A/G]tttgcactgtgtgtg | 7410 |
rs557500 | snp | C/T | 0.452965 | 0.145963 | intron-variant | VAV2 | GRCh38.p7 | 9:133953297 | GCTTGGGGGGCACAG[C/T]GCCAAGGGCACAGGA | 7410 |
rs561257 | snp | A/C | 0.483995 | 0.0880135 | intron-variant | VAV2 | GRCh38.p7 | 9:133947129 | GCCTTCCAAGACGTC[A/C]GGGGCCCCCAAGGAC | 7410 |
rs562000 | snp | C/G | 0.483995 | 0.0880135 | intron-variant | VAV2 | GRCh38.p7 | 9:133947161 | GCCACTGCTGCTTAG[C/G]TGGCAACCTCGCTTC | 7410 |
rs562143 | snp | C/G | 0.421209 | 0.182174 | intron-variant | VAV2 | GRCh38.p7 | 9:133929870 | AGGCAGGTTTCCTCA[C/G]CTGTGACGGATCAAT | 7410 |
rs567208 | snp | C/T | 0.42574 | 0.177808 | intron-variant | VAV2 | GRCh38.p7 | 9:133957167 | CCGTAACTGCCAGGC[C/T]GAGCCTCAGTTTCCC | 7410 |
rs578151 | snp | C/G | 0.496245 | 0.0431677 | intron-variant | VAV2 | GRCh38.p7 | 9:133950406 | GCCGCCCAGCCGTGC[C/G]TGTTCAGAGCCAGCA | 7410 |
rs581622 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | VAV2 | GRCh38.p7 | 9:133773336 | gacagctgtatgggg[C/T]gcttatcatgactgg | 7410 |
rs582682 | snp | A/G | 0.41023 | 0.191902 | intron-variant | VAV2 | GRCh38.p7 | 9:133773602 | acacagctgtacaaa[A/G]atattttattctttg | 7410 |
rs583505 | snp | C/T | 0.498852 | 0.0239341 | intron-variant | VAV2 | GRCh38.p7 | 9:133915383 | CACGATCTGGCGTTC[C/T]ACAGACTCCACCTGC | 7410 |
rs583538 | snp | A/C | 0.499809 | 0.00978247 | intron-variant | VAV2 | GRCh38.p7 | 9:133773755 | AGTATTTTTTTGCTG[A/C]GTAGAAGGAGTATGC | 7410 |
rs584396 | snp | A/G | 0.46014 | 0.13543 | intron-variant | VAV2 | GRCh38.p7 | 9:133960545 | AAATAATTGGCGGCC[A/G]CTATTAAGCGGAGAC | 7410 |
rs584738 | snp | A/G | 0.478768 | 0.100824 | intron-variant | VAV2 | GRCh38.p7 | 9:133928105 | CTGGAAAGGAAAGCA[A/G]AGAAAAACCTCTCCC | 7410 |
rs590614 | snp | C/T | 0.499121 | 0.020948 | intron-variant | VAV2 | GRCh38.p7 | 9:133770287 | CCTGCCCTCACAGAC[C/T]CAGACCAGGAGTCCC | 7410 |
rs591797 | snp | C/T | 0.419296 | 0.183954 | intron-variant | VAV2 | GRCh38.p7 | 9:133765682 | catattcaaatctta[C/T]cagtcatcccaatca | 7410 |
rs591866 | snp | A/G | 0.419296 | 0.183954 | intron-variant | VAV2 | GRCh38.p7 | 9:133765629 | CTGGTCCTGGATCCA[A/G]TCCAGGATCATGAAT | 7410 |
rs592252 | snp | C/T | 0.419296 | 0.183954 | intron-variant | VAV2 | GRCh38.p7 | 9:133765586 | ctgtgatccttaact[C/T]tctttaatctggaat | 7410 |
rs592820 | snp | C/T | 0.41325 | 0.18934 | intron-variant | VAV2 | GRCh38.p7 | 9:133765414 | tggggacgttggcac[C/T]ttctcagtgccgtag | 7410 |
rs593590 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | VAV2 | GRCh38.p7 | 9:133765276 | TGACTGTAATTAGCA[A/G]GTAATTTGCAGGGTA | 7410 |
rs594130 | snp | A/G | 0.416545 | 0.186448 | intron-variant | VAV2 | GRCh38.p7 | 9:133765106 | agttggcattctact[A/G]taaggaaaactttct | 7410 |
rs595291 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | VAV2 | GRCh38.p7 | 9:133913431 | TGTCAGGGGTGGTGC[A/G]CGCTTCCTGGTGCCC | 7410 |
rs598184 | snp | C/T | 0.480223 | 0.0974544 | intron-variant | VAV2 | GRCh38.p7 | 9:133914054 | ACAAGCAACCAAAGA[C/T]GATGCTCACCGCAAA | 7410 |
rs601764 | snp | C/T | 0.451856 | 0.147493 | intron-variant | VAV2 | GRCh38.p7 | 9:133967793 | caaaaattagccgga[C/T]gtggtggtgtgcacc | 7410 |
rs602990 | snp | C/T | 0.499995 | 0.00158753 | missense | VAV2 | GRCh38.p7 | 9:133778872 | CATGGTAATTCTGCA[C/T]GGCCACCATCTTGGG | 7410 |
rs603601 | snp | C/T | 0.481932 | 0.0933148 | intron-variant | VAV2 | GRCh38.p7 | 9:133932785 | CACTGCACCTGCCTT[C/T]TGGTGCCTCCTCTCA | 7410 |
rs604481 | snp | A/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133827427 | CCGCTGCGCCCACTG[A/G]GGCTGACCACTGAGC | 7410 |
rs604525 | snp | A/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133827452 | CTGAGCGGGGGCATC[A/G]CCAGCTACTGCTGTG | 7410 |
rs605476 | snp | C/G | 0.5 | 0.235702 | intron-variant | VAV2 | GRCh38.p7 | 9:133828416 | GTGGGGGCATCACCA[C/G]CTACCGCTGCGCCCA | 7410 |
rs605855 | snp | A/G | 0.21875 | 0.248039 | intron-variant | VAV2 | GRCh38.p7 | 9:133828460 | CTGAGTGGGGGCATC[A/G]CCACCTACCGCTGCG | 7410 |
rs605858 | snp | A/C/G | 0.402778 | 0.265347 | intron-variant | VAV2 | GRCh38.p7 | 9:133828464 | GTGGGGGCATCACCA[A/C/G]CTACCGCTGCGCCCA | 7410 |
rs608402 | snp | A/G | 0.491051 | 0.0662916 | intron-variant | VAV2 | GRCh38.p7 | 9:133914031 | ACATTATCCTGAAAC[A/G]TAAACCAACAAGCAA | 7410 |
rs608968 | snp | C/T | 0.494568 | 0.0518327 | intron-variant | VAV2 | GRCh38.p7 | 9:133920718 | AGGCGGGGGATGCTG[C/T]CTGTCACTGTCTCCC | 7410 |
rs609691 | snp | A/G | 0.488786 | 0.0740357 | intron-variant | VAV2 | GRCh38.p7 | 9:133913757 | CAGGCCTTGGGCACC[A/G]CGCCCAGGTCAGTGA | 7410 |
rs610173 | snp | G/T | 0.492037 | 0.0625946 | intron-variant | VAV2 | GRCh38.p7 | 9:133978185 | CCTCCCTGGCCCGCC[G/T]GCCAGAGGATGCTGG | 7410 |
rs611072 | snp | A/G | 0.476746 | 0.10529 | intron-variant | VAV2 | GRCh38.p7 | 9:133977990 | GCGTCCACCTGCCCT[A/G]GGGCACGCAGCTCCC | 7410 |
rs618439 | snp | A/G | 0.309401 | 0.24284 | intron-variant | VAV2 | GRCh38.p7 | 9:133971074 | CGCGGTGCCTCCTGC[A/G]GGGAGTGGGGACACC | 7410 |
rs619173 | snp | A/G | 0.4711 | 0.116682 | intron-variant | VAV2 | GRCh38.p7 | 9:133942552 | AAAAATAGTCACGCC[A/G]GGCTGGAAGCTGCAG | 7410 |
rs620986 | snp | C/T | 0.21875 | 0.248039 | intron-variant | VAV2 | GRCh38.p7 | 9:133828412 | CGCAGCGGTAGGTGG[C/T]GATGCCCCCACTCAG | 7410 |
rs621569 | snp | A/G | 0.482979 | 0.0906686 | intron-variant | VAV2 | GRCh38.p7 | 9:133949323 | TCCAACACTTTCCAC[A/G]AGGTCTCCTGGCCAC | 7410 |
rs622035 | snp | A/C | 0.31357 | 0.241783 | intron-variant | VAV2 | GRCh38.p7 | 9:133767540 | AATGCCAATCACACA[A/C]GGACCACTTTGAGAA | 7410 |
rs622543 | snp | A/G | 0.482159 | 0.0927485 | intron-variant | VAV2 | GRCh38.p7 | 9:133949586 | TGGAGTGTGGTGAGC[A/G]GGTGACCCGCCATTC | 7410 |
rs624234 | snp | C/T | 0.482979 | 0.0906686 | intron-variant | VAV2 | GRCh38.p7 | 9:133921802 | GTATAAGAAATCAAC[C/T]GCGGATGAACTTGAG | 7410 |
rs625083 | snp | C/G | 0.481165 | 0.0951993 | intron-variant | VAV2 | GRCh38.p7 | 9:133977185 | TCAGGCAGAGTGAGG[C/G]CCCCCCAGCATCCCA | 7410 |
rs625958 | snp | A/G | 0.497933 | 0.032082 | intron-variant | VAV2 | GRCh38.p7 | 9:133976987 | TGCCTGGACACCCCA[A/G]GGCTGAAGGGGGTGC | 7410 |
rs626547 | snp | A/G | 0.435119 | 0.16802 | intron-variant | VAV2 | GRCh38.p7 | 9:133925576 | GGGCTCTAGCCCCAA[A/G]GTCCCCAGGGGCAGA | 7410 |
rs629046 | snp | C/T | 0.483708 | 0.088773 | intron-variant | VAV2 | GRCh38.p7 | 9:133931695 | CTGCCTGTGACCCGG[C/T]GCCCAGGAGGCTCTG | 7410 |
rs632626 | snp | C/G | 0.412416 | 0.190055 | intron-variant | VAV2 | GRCh38.p7 | 9:133930872 | CTCTCAGCACTGTCT[C/G]GGGGTGGCTCCATGG | 7410 |
rs635277 | snp | C/G | 0.428786 | 0.174744 | intron-variant | VAV2 | GRCh38.p7 | 9:133957058 | GACACTGGTGGCGTT[C/G]GAGAGAGTCCTGGGT | 7410 |
rs635323 | snp | A/G | 0.425894 | 0.177655 | intron-variant | VAV2 | GRCh38.p7 | 9:133957088 | GTAGGCTTGCACAGA[A/G]TGAGGAACCAGAGAG | 7410 |
rs635739 | snp | A/G | 0.425432 | 0.178112 | intron-variant | VAV2 | GRCh38.p7 | 9:133957180 | GTACAGGGGAGGCCC[A/G]TAACTGCCAGGCCGA | 7410 |
rs636541 | snp | A/T | 0.48435 | 0.0870631 | intron-variant | VAV2 | GRCh38.p7 | 9:133950433 | GCGTGGAAAGCTGAG[A/T]CCTCTCTCAGCTGCT | 7410 |
rs636651 | snp | C/T | 0.425586 | 0.17796 | intron-variant | VAV2 | GRCh38.p7 | 9:133957385 | GAGACGACAGAAAAA[C/T]GCCCTCAGTGGTTAG | 7410 |
rs636667 | snp | C/T | 0.466618 | 0.124806 | intron-variant | VAV2 | GRCh38.p7 | 9:133957396 | CCCAGAGTCAAGAGA[C/T]GACAGAAAAACGCCC | 7410 |
rs637521 | snp | A/G | 0.444267 | 0.157354 | intron-variant | VAV2 | GRCh38.p7 | 9:133950703 | GAGGCGCAGGCGTGC[A/G]TCTGGGCTAATTGCT | 7410 |
rs639967 | snp | C/G | 0.465158 | 0.127307 | intron-variant | VAV2 | GRCh38.p7 | 9:133774621 | CCTGAGCTCACACAG[C/G]ATCTCACCCACCCAC | 7410 |
rs641803 | snp | C/G | 0.463234 | 0.130503 | intron-variant | VAV2 | GRCh38.p7 | 9:133918274 | AAACAAAGGAGCGCA[C/G]TCTCTGCGGCGGCAG | 7410 |
rs642193 | snp | A/C | 0.497211 | 0.037236 | downstream-variant-500B | VAV2 | GRCh38.p7 | 9:133761784 | TCTCAGACCCTGCTG[A/C]GGTTGGGCCACCCTG | 7410 |
rs643413 | snp | C/G | 0.498009 | 0.0314867 | intron-variant | VAV2 | GRCh38.p7 | 9:133910021 | ACACGagctatgcga[C/G]gccatgtgactagaa | 7410 |
rs648353 | snp | A/G | 0.429837 | 0.173662 | intron-variant | VAV2 | GRCh38.p7 | 9:133957705 | CACTTGGAGTGGCCC[A/G]GGCAGGGTGTCCCGG | 7410 |
rs649268 | snp | A/G | 0.425123 | 0.178415 | intron-variant | VAV2 | GRCh38.p7 | 9:133957904 | AGAGCACGGGGTTGG[A/G]GGTAAGGTCACAGAA | 7410 |
rs650830 | snp | C/T | 0.306182 | 0.243605 | intron-variant | VAV2 | GRCh38.p7 | 9:133782695 | CAAGACCCAGAGACT[C/T]GGCCTGGGGCCACCG | 7410 |
rs653373 | snp | A/G | 0.461037 | 0.134028 | intron-variant | VAV2 | GRCh38.p7 | 9:133951913 | ccaggctctggagct[A/G]caagaaagaagcccc | 7410 |
rs653967 | snp | A/G | 0.0603982 | 0.162945 | intron-variant | VAV2 | GRCh38.p7 | 9:133772076 | GTGTGGCCCTCACGC[A/G]GTGACCGCCGGGGCC | 7410 |
rs654182 | snp | C/T | 0.410737 | 0.191478 | intron-variant | VAV2 | GRCh38.p7 | 9:133952064 | GGACCATCCTATTCA[C/T]GAAGGGTCCGCTCTT | 7410 |
rs654387 | snp | A/C | 0.434253 | 0.168969 | intron-variant | VAV2 | GRCh38.p7 | 9:133938039 | GAGAAGTCGGTTCTG[A/C]GAGGAGCGTGTGGAA | 7410 |
rs656702 | snp | G/T | 0.495855 | 0.045338 | intron-variant | VAV2 | GRCh38.p7 | 9:133771439 | ATTGAGAACTCCTGA[G/T]TAGAGCCCCCAGGCT | 7410 |
rs662633 | snp | C/T | 0.383439 | 0.21141 | intron-variant | VAV2 | GRCh38.p7 | 9:133958542 | gacacatccccctct[C/T]ggagaaacacccacg | 7410 |
rs662645 | snp | C/T | 0.381503 | 0.21262 | intron-variant | VAV2 | GRCh38.p7 | 9:133958552 | cctctcggagaaaca[C/T]ccacgaatgaccaat | 7410 |
rs664026 | snp | A/G | 0.461813 | 0.132798 | intron-variant | VAV2 | GRCh38.p7 | 9:133958901 | CCTCGGGTTGTGACT[A/G]TCTCTTCCTGTGGGC | 7410 |
rs667183 | snp | A/G | 0.471182 | 0.116526 | intron-variant | VAV2 | GRCh38.p7 | 9:133776113 | TGTGAGTGGCCCTGG[A/G]GGGCCGTTAACACTC | 7410 |
rs669443 | snp | A/G | 0.451608 | 0.147832 | intron-variant | VAV2 | GRCh38.p7 | 9:133776591 | TTCCCCATCTGCATG[A/G]TGAATAGGGTGCGAG | 7410 |
rs675002 | snp | A/G | 0.427271 | 0.176281 | intron-variant | VAV2 | GRCh38.p7 | 9:133922041 | AGACGCCATGCATGC[A/G]GGCACGGGATGGGCC | 7410 |
rs677772 | snp | A/T | 0.487871 | 0.076925 | intron-variant | VAV2 | GRCh38.p7 | 9:133782875 | CCAGCTGCCCTGAGC[A/T]GGGCACAACCCCAAA | 7410 |
rs678744 | snp | C/T | 0.193966 | 0.243639 | intron-variant | VAV2 | GRCh38.p7 | 9:133974766 | CGGACAGATAGGTCA[C/T]GCCCTGCACCCAGCA | 7410 |
rs679106 | snp | A/C | 0.205417 | 0.245993 | intron-variant | VAV2 | GRCh38.p7 | 9:133974718 | CTCAGAAAATCCACA[A/C]ACTCCCTGCGCCCTG | 7410 |
rs679547 | snp | G/T | 0.202959 | 0.245534 | intron-variant | VAV2 | GRCh38.p7 | 9:133974611 | AAAGGTGGAGCAAGT[G/T]GCCCAAAGGCATGAG | 7410 |
rs679923 | snp | A/G | 0.491885 | 0.0631791 | intron-variant | VAV2 | GRCh38.p7 | 9:133906310 | GGACCTCTATTAAAC[A/G]CAGCCACATCTCCCA | 7410 |
rs680458 | snp | C/T | 0.391954 | 0.205789 | intron-variant | VAV2 | GRCh38.p7 | 9:133783443 | TGCTCACTTCTGCCC[C/T]CTACCACCTGGGTAC | 7410 |
rs681492 | snp | C/T | 0.445724 | 0.155538 | intron-variant | VAV2 | GRCh38.p7 | 9:133953625 | GCACTTGTGTGGAAC[C/T]TCAGACCCAGTTCCC | 7410 |
rs681508 | snp | C/T | 0.445724 | 0.155538 | intron-variant | VAV2 | GRCh38.p7 | 9:133953636 | GAACCTCAGACCCAG[C/T]TCCCTCTGACCACCA | 7410 |
rs681910 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133783796 | TCCACCAGCCTGCCT[C/T]CCTGCCCCACACAGC | 7410 |
rs682388 | snp | A/G | 0.445855 | 0.155373 | intron-variant | VAV2 | GRCh38.p7 | 9:133953798 | ATGACCCCGGCTCCC[A/G]GGCCTGCATGTCCAA | 7410 |
rs682418 | snp | C/T | 0.445855 | 0.155373 | intron-variant | VAV2 | GRCh38.p7 | 9:133953825 | CCAACAGCTGCCTCC[C/T]TGTCTCCAAAGAAGG | 7410 |
rs686319 | snp | C/T | 0.475081 | 0.108804 | intron-variant | VAV2 | GRCh38.p7 | 9:133919851 | CACCCCTGCCTCACC[C/T]ACCACCCAACCGCAT | 7410 |
rs687402 | snp | C/T | 0.369346 | 0.219673 | intron-variant | VAV2 | GRCh38.p7 | 9:133907134 | CGTCACTGCTCTTGG[C/T]AACATGTTTGGGGCC | 7410 |
rs687644 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | VAV2 | GRCh38.p7 | 9:133947212 | ACAAGCAAGCAGGTG[A/G]AAGGTAGGGTCTGGC | 7410 |
rs688091 | snp | C/G | 0.483563 | 0.0891524 | intron-variant | VAV2 | GRCh38.p7 | 9:133947282 | CAACTCTACACACCA[C/G]CCCACCAGGGACCCA | 7410 |
rs688828 | snp | A/G | 0.48978 | 0.0707512 | intron-variant | VAV2 | GRCh38.p7 | 9:133906768 | GACCCCGCTGCCCCC[A/G]GCTCTCCAGGCGCCA | 7410 |
rs694032 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133827442 | GGTGGTGATGCCCCC[A/G]CTCAGTGGTCAGCCC | 7410 |
rs694174 | snp | A/G | 0.404907 | 0.196224 | intron-variant | VAV2 | GRCh38.p7 | 9:133766256 | TAAACTAGTTCAACC[A/G]TTGTGGAAGACAGTG | 7410 |
rs694505 | snp | A/G | 0.410905 | 0.191336 | intron-variant | VAV2 | GRCh38.p7 | 9:133955952 | AGAGCTCCCCGGAGC[A/G]GGGGCCTCCAGCAGG | 7410 |
rs694511 | snp | C/T | 0.459347 | 0.136653 | intron-variant | VAV2 | GRCh38.p7 | 9:133955963 | CTGCCCGTCTGAGAG[C/T]TCCCCGGAGCGGGGG | 7410 |
rs694913 | snp | A/G | 0.412082 | 0.190341 | intron-variant | VAV2 | GRCh38.p7 | 9:133772474 | gacaggcttgcgctc[A/G]gcacctctgaggagc | 7410 |
rs695067 | snp | A/G | 0.430285 | 0.173197 | intron-variant | VAV2 | GRCh38.p7 | 9:133963739 | TAATTAGAGTTTCAC[A/G]GGCATTTTTTCCCCT | 7410 |
rs734997 | snp | C/G | 0.297636 | 0.24542 | intron-variant | VAV2 | GRCh38.p7 | 9:133951372 | GGGACACTTTTCAGG[C/G]TGAAAGCCCCACAGT | 7410 |
rs735520 | snp | C/T | 0.205723 | 0.246048 | intron-variant | VAV2 | GRCh38.p7 | 9:133849497 | CCCTCCTGGACCCTG[C/T]GTCCCAGAGCTGGCT | 7410 |
rs735521 | snp | C/T | 0.205723 | 0.246048 | intron-variant | VAV2 | GRCh38.p7 | 9:133849547 | CCTGCtgtgtttgtg[C/T]cctggggctgcgtaa | 7410 |
rs736688 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | VAV2 | GRCh38.p7 | 9:133813568 | AGCCACACGGCGTCC[A/G]TCTGTGGGCAAAGCA | 7410 |
rs739448 | snp | C/T | 0.375598 | 0.21616 | intron-variant | VAV2 | GRCh38.p7 | 9:133887442 | AAGATCCTGCCCTAA[C/T]TCTAAAAACAGCAAT | 7410 |
rs739449 | snp | A/G | 0.424814 | 0.178718 | intron-variant | VAV2 | GRCh38.p7 | 9:133943268 | CGGTCCCTGCCAACC[A/G]TCAGGGTCTCTGTCT | 7410 |
rs739450 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | VAV2 | GRCh38.p7 | 9:133813563 | GCACAAGCCACACGG[C/T]GTCCGTCTGTGGGCA | 7410 |
rs739451 | snp | C/T | 0.307176 | 0.243374 | intron-variant | VAV2 | GRCh38.p7 | 9:133813832 | AGAGCCACCGACCCA[C/T]GGGCAAGCCCCTCTG | 7410 |
rs739465 | snp | C/T | 0.338314 | 0.233882 | intron-variant | VAV2 | GRCh38.p7 | 9:133847000 | GGCCCACGGCTGGCA[C/T]CACCCACAGGGTCAA | 7410 |
rs739466 | snp | C/T | 0.40595 | 0.195396 | intron-variant | VAV2 | GRCh38.p7 | 9:133866305 | TAAAGAGGGATTCTA[C/T]GTGTTGGGGGGAGGG | 7410 |
rs745695 | snp | C/T | 0.495782 | 0.0457324 | intron-variant | VAV2 | GRCh38.p7 | 9:133911151 | AGGAATGTATTCACG[C/T]GTGCACTGGGGACCG | 7410 |
rs756776 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | VAV2 | GRCh38.p7 | 9:133957197 | CGGACCTGCAGCAGC[G/T]GGTACAGGGGAGGCC | 7410 |
rs756777 | snp | A/G | 0.386123 | 0.209692 | intron-variant | VAV2 | GRCh38.p7 | 9:133813958 | AAACTGAGGTTAAAC[A/G]GCCAGCAAGGGGCAG | 7410 |
rs756811 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | VAV2 | GRCh38.p7 | 9:133776982 | AAGCTAGACTTTATG[C/T]TATTTAAAACAGAGG | 7410 |
rs756812 | snp | C/G | 0.151334 | 0.229706 | intron-variant | VAV2 | GRCh38.p7 | 9:133775950 | CGCCGGGTCTGGGTG[C/G]TGCCTGTGAGCGGCC | 7410 |
rs803436 | snp | A/G | 0.391397 | 0.206172 | intron-variant | VAV2 | GRCh38.p7 | 9:133923780 | gattaagaaaatgtg[A/G]cacatatataccatg | 7410 |
rs803437 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | VAV2 | GRCh38.p7 | 9:133908079 | CCTTCTCTGCCTTCC[C/T]CCAGAGAGTGGAGGG | 7410 |
rs803438 | snp | A/G | 0.444444 | 0.157135 | intron-variant | VAV2 | GRCh38.p7 | 9:133910838 | aaaaaaaaaaaaaaa[A/G]aaaaagaaaaagaaA | 7410 |
rs803439 | snp | C/G | 0.421526 | 0.181876 | intron-variant | VAV2 | GRCh38.p7 | 9:133927907 | TATGGGTCTTTGCCT[C/G]AACCCTGCTCACAGG | 7410 |
rs803499 | snp | A/G | 0.219947 | 0.248187 | intron-variant | VAV2 | GRCh38.p7 | 9:133976068 | gaaaattagccaggc[A/G]tggtggtgggcacct | 7410 |
rs809151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV2 | GRCh38.p7 | 9:133893911 | ctttactggacctca[C/T]ggatcctcacagccc | 7410 |
rs809737 | snp | A/G | 0.236434 | 0.249632 | intron-variant | VAV2 | GRCh38.p7 | 9:133975702 | GCTGCTCACCCAAGA[A/G]CACAGAGGCACAGTG | 7410 |
rs810664 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | VAV2 | GRCh38.p7 | 9:133911060 | TGGCCAGGCTACATG[A/G]GCTGCAGGAAGCAGG | 7410 |
rs813015 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | VAV2 | GRCh38.p7 | 9:133884078 | aggcggaggttgcag[C/G/T]gaggcggaggttgca | 7410 |
rs813926 | snp | A/G | 0.478104 | 0.102316 | intron-variant | VAV2 | GRCh38.p7 | 9:133924017 | ACTAGGGGAGGGAGA[A/G]CATTAGGAGAAATAT | 7410 |
rs886018 | snp | C/T | 0.370365 | 0.219117 | intron-variant | VAV2 | GRCh38.p7 | 9:133947049 | AAGCACTCTTAGGTG[C/T]CCTCTGACTGCTGAC | 7410 |
rs886096 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | VAV2 | GRCh38.p7 | 9:133798304 | TTGCTTCCACATGGT[A/G]TCTGGATTCCACAAG | 7410 |
rs886112 | snp | A/C | 0.404035 | 0.196909 | intron-variant | VAV2 | GRCh38.p7 | 9:133905723 | CTCTGTAGTGGATCA[A/C]TGGGGCTGCAGCACA | 7410 |
rs998990 | snp | C/T | 0.29278 | 0.246313 | intron-variant | VAV2 | GRCh38.p7 | 9:133924260 | GGGAATTGGAGGTTG[C/T]GGTGAGCAGAGATAT | 7410 |
rs1005876 | snp | A/G | 0.489492 | 0.0717183 | intron-variant | VAV2 | GRCh38.p7 | 9:133801795 | tcgttctctgtcccc[A/G]tctccacatggcctc | 7410 |
rs1043077 | snp | C/T | 0.0744748 | 0.178019 | utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133763099 | AGAGGTTGGTTCCAG[C/T]CCCTGGCAGGGCTTC | 7410 |
rs1043104 | snp | A/C | 0 | 0 | utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133762254 | ATGATCACGAAGGAC[A/C]CTGAGAAAAAATAAT | 7410 |
rs1043113 | snp | C/T | 0 | 0 | utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133762008 | ATGTGGGTCAGGGAT[C/T]TGGGGGCCCCCCCAG | 7410 |
rs1062145 | snp | G/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133912780 | TTGTGATTTTAGAGG[G/T]GCTGAACAAGTACTT | 7410 |
rs1132455 | snp | C/T | | | synonymous-codon | VAV2 | GRCh38.p7 | 9:133770397 | GGACCGGCTGGAGGC[C/T]CTGGAGGCCGAACGT | 7410 |
rs1150060 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133869402 | ctcaggctggcctca[A/G]actcctggcttccag | 7410 |
rs1150061 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133856907 | CACACTCTCAGGGTT[C/T]GGGGGTTAGGACATC | 7410 |
rs1150062 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV2 | GRCh38.p7 | 9:133855250 | CAGTGTGCAGAGAGG[A/G]TAGCACATTCGTTCA | 7410 |
rs1150063 | snp | G/T | 0.078151 | 0.181571 | intron-variant | VAV2 | GRCh38.p7 | 9:133852609 | ACACAGGCAGATCCC[G/T]GCCCCACTGCAGAAG | 7410 |
rs1179486 | snp | A/G | 0.130694 | 0.219696 | intron-variant | VAV2 | GRCh38.p7 | 9:133851277 | gatccccatttgcag[A/G]ggaggaacctgaggc | 7410 |
rs1179487 | snp | A/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133851911 | gatggatggatgggt[A/G]gatggatggatggat | 7410 |
rs1179488 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV2 | GRCh38.p7 | 9:133852039 | aaggatgtatggatg[G/T]atggatgtatggatg | 7410 |
rs1182879 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133884044 | gggttcaagtgattc[C/T]cctgcctcagcctcc | 7410 |
rs1468127 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | VAV2 | GRCh38.p7 | 9:133786659 | GGGATGGCTTCACGG[A/G]GGGTGCCCCAGGCCC | 7410 |
rs1468128 | snp | C/T | 0.399086 | 0.200682 | intron-variant | VAV2 | GRCh38.p7 | 9:133783484 | AGTACCCCCCTCACC[C/T]CCCCACCCCAGTCCC | 7410 |
rs1548380 | snp | C/G | 0.117886 | 0.21224 | intron-variant | VAV2 | GRCh38.p7 | 9:133803271 | CCTCCCAAAAGCGCT[C/G]GTGCAAAGCTCCACA | 7410 |
rs1548381 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | VAV2 | GRCh38.p7 | 9:133803272 | CTCCCAAAAGCGCTC[A/G]TGCAAAGCTCCACAG | 7410 |
rs1557678 | snp | C/T | 0.407502 | 0.194147 | intron-variant | VAV2 | GRCh38.p7 | 9:133849999 | CCATACACCCCCTTC[C/T]CTCAGGCTTGTCTGG | 7410 |
rs1557679 | snp | C/T | 0.407502 | 0.194147 | intron-variant | VAV2 | GRCh38.p7 | 9:133850001 | ATACACCCCCTTCTC[C/T]CAGGCTTGTCTGGGA | 7410 |
rs1572751 | snp | C/G | 0.246769 | 0.249979 | intron-variant | VAV2 | GRCh38.p7 | 9:133805253 | ACTCCCCAGGCCCCA[C/G]AGCAGACCCAGACCC | 7410 |
rs1572752 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | VAV2 | GRCh38.p7 | 9:133799902 | CAGGTGCAGGCGGCC[G/T]CCGGGAGTCAGTGTC | 7410 |
rs1631312 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133941760 | aaaaattagctgggc[A/G]tggtggtgcgtgcct | 7410 |
rs1633757 | snp | G/T | 0.430434 | 0.173042 | intron-variant | VAV2 | GRCh38.p7 | 9:133943510 | CAGTGGCTGCCTTTG[G/T]GGGGGGTCCCGAAGG | 7410 |
rs1633759 | snp | C/T | 0.451483 | 0.148002 | intron-variant | VAV2 | GRCh38.p7 | 9:133954166 | TTGACTCTTTCTTCT[C/T]GAAATGATGGGTGCT | 7410 |
rs1633763 | snp | C/T | 0.459914 | 0.13578 | intron-variant | VAV2 | GRCh38.p7 | 9:133952512 | gggttcaagtaattc[C/T]cctgcctcagcctcc | 7410 |
rs1633764 | snp | C/G | 0.460027 | 0.135605 | intron-variant | VAV2 | GRCh38.p7 | 9:133952326 | gtgagccaccgcacc[C/G]ggccTTGAGAGCATC | 7410 |
rs1768685 | snp | A/G | 0.478932 | 0.10045 | intron-variant | VAV2 | GRCh38.p7 | 9:133947377 | ACAGATGAGGAGACC[A/G]AGACTCAGGGAGGCC | 7410 |
rs1858866 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | VAV2 | GRCh38.p7 | 9:133776471 | CACCGGAGCGGCAGC[A/G]CCTGCCTGAGTGTGG | 7410 |
rs1890602 | snp | A/G | | | | | GRCh38.p7 | 9:133813527 | AGCGTGTCCTCCAGG[A/G]AAGGTGCTGAGGGCC | 7410 |
rs1893602 | snp | C/T | 0.493386 | 0.0571263 | | | GRCh38.p7 | 9:133794667 | CAGCCCTGAGGGGGG[C/T]TGGCAGAGGTGTCCT | 7410 |
rs2011725 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | VAV2 | GRCh38.p7 | 9:133905896 | AATACAGAAATTAGC[C/T]GGGCGTGGTGGTACA | 7410 |
rs2023664 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | VAV2 | GRCh38.p7 | 9:133786063 | GCACGTGTGCACGTA[C/T]AGCATGGGCAAGAGA | 7410 |
rs2023665 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | VAV2 | GRCh38.p7 | 9:133785618 | CCATCACCCCTGGGA[C/T]GCCAGCCTCAAGCAG | 7410 |
rs2072059 | snp | C/T | 0.493524 | 0.0565351 | intron-variant | VAV2 | GRCh38.p7 | 9:133789375 | CTGGGGCTGCTCCAG[C/T]CCCGGCTGACGGCCC | 7410 |
rs2073829 | snp | A/G | 0.448066 | 0.152544 | intron-variant | VAV2 | GRCh38.p7 | 9:133961335 | AAGCTTCGGCCTGTG[A/G]CCAAGACACCATGGG | 7410 |
rs2073830 | snp | C/T | 0.323197 | 0.239044 | intron-variant | VAV2 | GRCh38.p7 | 9:133870252 | CTGCACTCTGCCGGC[C/T]CCCTAGAAGAAACTT | 7410 |
rs2073883 | snp | C/T | 0.333722 | 0.235565 | intron-variant | VAV2 | GRCh38.p7 | 9:133888954 | CGCAAGGAGACGACA[C/T]GAACAGCATGGAAAT | 7410 |
rs2073884 | snp | C/T | 0.434109 | 0.169127 | intron-variant | VAV2 | GRCh38.p7 | 9:133956257 | GGATCATGGCACCTC[C/T]GGAGATCATCGAGTT | 7410 |
rs2073885 | snp | A/G | 0.368938 | 0.219895 | intron-variant | VAV2 | GRCh38.p7 | 9:133949369 | CCCAGCCCACCTTGA[A/G]TGAACCAAAGCTGGA | 7410 |
rs2073886 | snp | C/T | 0.379923 | 0.213588 | intron-variant | VAV2 | GRCh38.p7 | 9:133939089 | AGGTGAGCAGTCACT[C/T]TCTCCAGCCTCGGTC | 7410 |
rs2073887 | snp | C/G | 0.440471 | 0.161928 | intron-variant | VAV2 | GRCh38.p7 | 9:133938504 | CCTGCATGCAGGAGC[C/G]GGGCTGGTGCACATG | 7410 |
rs2073888 | snp | C/T | 0.492918 | 0.0590819 | intron-variant | VAV2 | GRCh38.p7 | 9:133793694 | TGAGGGAAATGTCTG[C/T]ACTTTGATACAGAGG | 7410 |
rs2073889 | snp | G/T | 0.492871 | 0.0592773 | intron-variant | VAV2 | GRCh38.p7 | 9:133793815 | CTCAAAGACGCTGCC[G/T]TACAAGGAGTGAGCC | 7410 |
rs2073890 | snp | C/T | 0.492871 | 0.0592773 | intron-variant | VAV2 | GRCh38.p7 | 9:133793830 | GTACAAGGAGTGAGC[C/T]CTCAGTCCCTAGGGG | 7410 |
rs2073891 | snp | C/T | 0.493523 | 0.0565391 | intron-variant | VAV2 | GRCh38.p7 | 9:133793877 | CAGCGACGACTCCCA[C/T]AGTGGCTGCATGAAT | 7410 |
rs2073892 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | VAV2 | GRCh38.p7 | 9:133794051 | CACTCCTGGGAAACC[A/G]TCCCGTCGAGGGGCT | 7410 |
rs2073909 | snp | A/C | 0.490508 | 0.0682328 | intron-variant | VAV2 | GRCh38.p7 | 9:133786369 | CCCACAGGAGAGCAC[A/C]CACAGGAGAGCACCC | 7410 |
rs2073910 | snp | G/T | 0.48978 | 0.0707512 | intron-variant | VAV2 | GRCh38.p7 | 9:133786306 | CATCATACGTGTTAG[G/T]ACATGTGTGTACCTG | 7410 |
rs2073928 | snp | C/G | 0.184521 | 0.241273 | intron-variant | VAV2 | GRCh38.p7 | 9:133855308 | CAAGGCCCATTCACG[C/G]AGCCTCCGGCTGAGA | 7410 |
rs2073929 | snp | C/G | 0.183886 | 0.241099 | intron-variant | VAV2 | GRCh38.p7 | 9:133855463 | AGCCAGCAAGGCACG[C/G]GGTTCCAGTGCTCTC | 7410 |
rs2073930 | snp | A/C | 0.160938 | 0.233598 | intron-variant | VAV2 | GRCh38.p7 | 9:133855579 | CCCGGCCTCTCCCTG[A/C]ACGAGCCGCATCTTA | 7410 |
rs2073931 | snp | A/C | 0.105569 | 0.204058 | intron-variant | VAV2 | GRCh38.p7 | 9:133863468 | GAGACAGAGAGGAGG[A/C]GTGGCGGGCGAGCCA | 7410 |
rs2077065 | snp | C/G | 0.279195 | 0.248289 | intron-variant | VAV2 | GRCh38.p7 | 9:133776191 | TCCACAGACAGTCCC[C/G]TCCAGGGCAGCCAAT | 7410 |
rs2077384 | snp | A/G | 0.370568 | 0.219005 | intron-variant | VAV2 | GRCh38.p7 | 9:133943332 | CGGCCTGTGTCCTCA[A/G]TGGGCCCCTGTGGCC | 7410 |
rs2077392 | snp | A/G | 0.115788 | 0.21092 | intron-variant | VAV2 | GRCh38.p7 | 9:133814335 | CAGTCACTTGCCTGC[A/G]TCCCTGGTAGCCTGG | 7410 |
rs2078831 | snp | A/C | 0.0136048 | 0.0813469 | intron-variant | VAV2 | GRCh38.p7 | 9:133776834 | AGAGTGAGAGCGTGG[A/C]ACCTCTGAAGGTGCA | 7410 |
rs2078832 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133776781 | GCGGCAGCCCCGGTG[A/C]TCCCCGACCCCAGCC | 7410 |
rs2078833 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133776588 | cccatctgcatgatg[A/C]ATAGGGTGCGAGGGA | 7410 |
rs2106225 | snp | A/G | 0.26271 | 0.249677 | intron-variant | VAV2 | GRCh38.p7 | 9:133922851 | GAAAACAGACAAATG[A/G]GACTACATCAGACTC | 7410 |
rs2106373 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | VAV2 | GRCh38.p7 | 9:133786837 | TCCCTCCCTTCGTTC[C/T]TCTTTCCCGCCATCT | 7410 |
rs2106395 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133848736 | GCTGGGGGTGAGGCA[A/G]ACAGCTCTGGGCCCA | 7410 |
rs2156323 | snp | C/T | 0.160609 | 0.233472 | intron-variant | VAV2 | GRCh38.p7 | 9:133855699 | TGGAAGCAGTGACCT[C/T]GCATTTCCTTATGGC | 7410 |
rs2157834 | snp | A/C | 0.248471 | 0.249995 | intron-variant | VAV2 | GRCh38.p7 | 9:133902179 | ATTGGCCTCCCTGAG[A/C]CCCAACTTCATTGTC | 7410 |
rs2157835 | snp | G/T | 0.258843 | 0.249844 | intron-variant | VAV2 | GRCh38.p7 | 9:133902224 | GGAACGGGCATCTGC[G/T]TCGGACGTGTGAGGA | 7410 |
rs2157836 | snp | A/C | 0.434687 | 0.168495 | intron-variant | VAV2 | GRCh38.p7 | 9:133902662 | AGATACATAGGGGTG[A/C]TAATCCCCAGGACCT | 7410 |
rs2239912 | snp | C/T | 0.487113 | 0.0792303 | intron-variant | VAV2 | GRCh38.p7 | 9:133793369 | GGTTCCCATCCCTCC[C/T]GCCCTTCCTCGTTCC | 7410 |
rs2239913 | snp | A/G | 0.492871 | 0.0592773 | intron-variant | VAV2 | GRCh38.p7 | 9:133793809 | CTGATTCTCAAAGAC[A/G]CTGCCGTACAAGGAG | 7410 |
rs2256875 | snp | C/T | 0.436692 | 0.166271 | intron-variant | VAV2 | GRCh38.p7 | 9:133952835 | GGTTGCACAGCCCCA[C/T]TGACACCTAGAACCT | 7410 |
rs2256876 | snp | A/C | 0.446118 | 0.155041 | intron-variant | VAV2 | GRCh38.p7 | 9:133952932 | CTGGAGGGAGCATGG[A/C]CCCCGGGACACCTAG | 7410 |
rs2258889 | snp | A/G | 0.49168 | 0.063958 | intron-variant | VAV2 | GRCh38.p7 | 9:133787343 | GGTGCCGCAGTGTGG[A/G]GGCGCCAGGAGCCCT | 7410 |
rs2259731 | snp | G/T | 0.338069 | 0.233974 | intron-variant | VAV2 | GRCh38.p7 | 9:133934146 | ggataaatggatgga[G/T]gagtgaatgaacgaa | 7410 |
rs2260095 | snp | A/G | 0.358303 | 0.225323 | intron-variant | VAV2 | GRCh38.p7 | 9:133840834 | CGATGGCGTCTGCAG[A/G]GCACCACCTGTGCCA | 7410 |
rs2261150 | snp | C/G | 0.403509 | 0.197319 | intron-variant | VAV2 | GRCh38.p7 | 9:133853134 | CCAGGACAGCAGGAA[C/G]AGGTTCAAAGCCTTC | 7410 |
rs2261166 | snp | C/T | 0.248471 | 0.249995 | intron-variant | VAV2 | GRCh38.p7 | 9:133925620 | CTGCATGTTTCGCCA[C/T]TGCCCTTGCTGCTGG | 7410 |
rs2261613 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | VAV2 | GRCh38.p7 | 9:133786163 | GCAGGAGCACACTAG[C/T]ATGCATGCAGAGGTG | 7410 |
rs2261783 | snp | A/G | 0.372794 | 0.217765 | intron-variant | VAV2 | GRCh38.p7 | 9:133899101 | gctgggattacaggc[A/G]tgagccaccgcgcca | 7410 |
rs2262143 | snp | A/G | 0.171704 | 0.237423 | intron-variant | VAV2 | GRCh38.p7 | 9:133899111 | caggcgtgagccacc[A/G]cgccaggccCAGACC | 7410 |
rs2263807 | snp | G/T | 0.372995 | 0.217652 | intron-variant | VAV2 | GRCh38.p7 | 9:133941899 | agtggaatcaCggcc[G/T]ggcgtggtggctcac | 7410 |
rs2265520 | snp | C/T | 0.496314 | 0.0427728 | intron-variant | VAV2 | GRCh38.p7 | 9:133925160 | tgggaatctgttcga[C/T]gctgctgaaatgcac | 7410 |
rs2265521 | snp | C/T | 0.097727 | 0.198275 | intron-variant | VAV2 | GRCh38.p7 | 9:133925252 | gacagggtctcgctc[C/T]gttgcccagactgga | 7410 |
rs2283127 | snp | A/C | 0.382085 | 0.212258 | intron-variant | VAV2 | GRCh38.p7 | 9:133825253 | ACCCGCCTTAAGAAA[A/C]GCCCCGTCTTCCGTC | 7410 |
rs2318820 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | VAV2 | GRCh38.p7 | 9:133798705 | AAGGATGACAAGAGC[C/T]ACCACTCGCTGAGGC | 7410 |
rs2319056 | snp | A/G | 0.460252 | 0.135255 | intron-variant | VAV2 | GRCh38.p7 | 9:133952737 | gaggcacagattggc[A/G]tgatgcagccacaag | 7410 |
rs2319057 | snp | C/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133952861 | AACCTGGAGGGAGCA[C/T]GGCCCCCGGGACACC | 7410 |
rs2319059 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133952903 | GGGAGCACGGCCCCA[C/G]TGACACCTAGAACCT | 7410 |
rs2319060 | snp | G/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133952904 | GGAGCACGGCCCCAC[G/T]GACACCTAGAACCTG | 7410 |
rs2319061 | snp | A/C/T | 0.0197687 | 0.0974348 | intron-variant | VAV2 | GRCh38.p7 | 9:133952936 | AGGGAGCATGGACCC[A/C/T]GGGACACCTAGAACC | 7410 |
rs2319062 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV2 | GRCh38.p7 | 9:133952937 | GGGAGCATGGACCCC[A/C/G]GGACACCTAGAACCT | 7410 |
rs2319063 | snp | G/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133952938 | GGAGCATGGACCCCG[G/T]GACACCTAGAACCTG | 7410 |
rs2319064 | snp | C/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133953004 | AGGGAGCATGGCCCC[C/T]GGGACACCTAGAACC | 7410 |
rs2319065 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953038 | AGGGAGCACGGCCCC[A/C]CTGACACCTAGAACC | 7410 |
rs2319066 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953039 | GGGAGCACGGCCCCA[C/G]TGACACCTAGAACCT | 7410 |
rs2428003 | snp | C/T | 0.227664 | 0.249 | intron-variant | VAV2 | GRCh38.p7 | 9:133938127 | GAGCATTTCCTTAGA[C/T]ACCAAGTCCCTGATA | 7410 |
rs2428004 | snp | A/G | 0.396182 | 0.202807 | intron-variant | VAV2 | GRCh38.p7 | 9:133941696 | caacctctgcctccc[A/G]ggttcaagcgaattc | 7410 |
rs2428005 | snp | C/T | 0.425894 | 0.177655 | intron-variant | VAV2 | GRCh38.p7 | 9:133955482 | ATGCTGCCCCAACTC[C/T]CCCCATGCTCCTCAG | 7410 |
rs2428082 | snp | C/T | 0.470811 | 0.117228 | intron-variant | VAV2 | GRCh38.p7 | 9:133893464 | TCTGGGGTCCTCAGG[C/T]GGCAAGGGACCTGCC | 7410 |
rs2428083 | snp | A/G | 0.385741 | 0.209939 | intron-variant | VAV2 | GRCh38.p7 | 9:133915379 | TCAGCACGATCTGGC[A/G]TTCTACAGACTCCAC | 7410 |
rs2428086 | snp | A/G | 0.289683 | 0.24683 | intron-variant | VAV2 | GRCh38.p7 | 9:133970591 | GGGCTGCAGAGATGG[A/G]GGTGGCTCCTTCCCT | 7410 |
rs2428088 | snp | C/T | 0.490119 | 0.0695896 | intron-variant | VAV2 | GRCh38.p7 | 9:133806819 | CCACCCATGCACGGC[C/T]GCCGGAGCCTGGTGC | 7410 |
rs2428089 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | VAV2 | GRCh38.p7 | 9:133807407 | CCAGGGGAGGGTCCC[A/G]GGGCAGCTCCGAGGC | 7410 |
rs2428090 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV2 | GRCh38.p7 | 9:133807883 | GACGTGTGAGGCTGC[C/T]GACCCTGCTCTGGAG | 7410 |
rs2428091 | snp | G/T | 0.493969 | 0.05458 | intron-variant | VAV2 | GRCh38.p7 | 9:133808563 | TGCACAAGAGTGGAA[G/T]AGCTGGGCAAGGAGC | 7410 |
rs2428092 | snp | C/T | 0.251578 | 0.249995 | intron-variant | VAV2 | GRCh38.p7 | 9:133824719 | GGGCAGGGAGGGCTC[C/T]TTTAGCCACCCCTGG | 7410 |
rs2428093 | snp | A/C | 0.134119 | 0.221521 | intron-variant | VAV2 | GRCh38.p7 | 9:133825163 | AGACAATGCCACGGT[A/C]CAGCCAGGTGTCCTT | 7410 |
rs2428094 | snp | C/T | 0.158962 | 0.232835 | intron-variant | VAV2 | GRCh38.p7 | 9:133825735 | CTCACTCCTTGTACC[C/T]CTGCAGACAAAGGGC | 7410 |
rs2428095 | snp | A/C | 0.144969 | 0.226867 | intron-variant | VAV2 | GRCh38.p7 | 9:133826023 | ACATTACATTCCCTG[A/C]CGTGTCACGATCACA | 7410 |
rs2428096 | snp | C/T | 0.14665 | 0.227637 | intron-variant | VAV2 | GRCh38.p7 | 9:133826435 | GAAGCCAGGAGGACA[C/T]GCGGTTCCTGACAGA | 7410 |
rs2428098 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | VAV2 | GRCh38.p7 | 9:133796103 | GGCTTTCCTGAAGCC[C/T]TTCCATGTCCATTTC | 7410 |
rs2428099 | snp | C/T | 0.488786 | 0.0740357 | intron-variant | VAV2 | GRCh38.p7 | 9:133796812 | CGCCTGCTGGGCCTG[C/T]CTGGATGTGGCCTTG | 7410 |
rs2428100 | snp | A/G | 0.490997 | 0.0664859 | intron-variant | VAV2 | GRCh38.p7 | 9:133798889 | CAGCGTCCTGGTGAT[A/G]TGCTCTCTGGCAGGG | 7410 |
rs2428101 | snp | A/C | 0.108048 | 0.20579 | intron-variant | VAV2 | GRCh38.p7 | 9:133905968 | TCTCTTGAGCCTGGG[A/C]GGTAGAGGCTGTAGT | 7410 |
rs2428105 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | VAV2 | GRCh38.p7 | 9:133773212 | cgggagcaataggct[C/T]tgccgtccagcctag | 7410 |
rs2428107 | snp | A/T | 0.181978 | 0.240568 | intron-variant | VAV2 | GRCh38.p7 | 9:133783324 | CACGTCACACACTTA[A/T]CAGGAGACACAGCCG | 7410 |
rs2428108 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | VAV2 | GRCh38.p7 | 9:133782554 | TGATTTTAGATCAAT[A/G]GTTAATTCACCATTT | 7410 |
rs2428118 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | VAV2 | GRCh38.p7 | 9:133841874 | GGGTCTCTCCCCTTC[C/T]GCTTTCCACCAGCTC | 7410 |
rs2428119 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | VAV2 | GRCh38.p7 | 9:133842113 | AGAAGGTACAGAAAT[C/G]AGTGCTTGGCTCATC | 7410 |
rs2428120 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | VAV2 | GRCh38.p7 | 9:133845203 | ACGTGTGTCCCACCC[C/T]GGCCAGAGGCAGAAG | 7410 |
rs2428121 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | VAV2 | GRCh38.p7 | 9:133845565 | CACTTCCTGCCGACT[C/T]GTCTGCTGGGAAATG | 7410 |
rs2428122 | snp | C/T | 0.103794 | 0.20279 | intron-variant | VAV2 | GRCh38.p7 | 9:133846813 | GTGAACATGACTGGC[C/T]GACGGGCGGCAGGGA | 7410 |
rs2428123 | snp | C/T | 0.391583 | 0.206044 | intron-variant | VAV2 | GRCh38.p7 | 9:133848874 | ACCACAACCTGAATG[C/T]ATGACCACAGTCCCC | 7410 |
rs2428124 | snp | A/G | 0.349671 | 0.229272 | intron-variant | VAV2 | GRCh38.p7 | 9:133850808 | GAAGCTCACACCCTC[A/G]GGCTCTTCCTCAAAC | 7410 |
rs2428125 | snp | C/T | 0.117537 | 0.212022 | intron-variant | VAV2 | GRCh38.p7 | 9:133851197 | CTTTGCAGCCATGTG[C/T]CGCATGGAAAGTCTG | 7410 |
rs2428126 | snp | A/G | 0.399253 | 0.200558 | intron-variant | VAV2 | GRCh38.p7 | 9:133851619 | ACACTGAGACCAATC[A/G]CGTTATATTCATGTG | 7410 |
rs2428127 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV2 | GRCh38.p7 | 9:133851749 | gaatgggtggatggg[C/T]atattgggtggatgc | 7410 |
rs2428129 | snp | C/T | 0.398534 | 0.201091 | intron-variant | VAV2 | GRCh38.p7 | 9:133855087 | CCGGATGGAAGAGAG[C/T]GGAGAGAGCAGGGGA | 7410 |
rs2486330 | snp | C/G | 0.494013 | 0.0543839 | intron-variant | VAV2 | GRCh38.p7 | 9:133809399 | GGCTTGGAGGCAGAG[C/G]CTTCTAGAATCCCAG | 7410 |
rs2486331 | snp | C/G | 0.439363 | 0.163222 | intron-variant | VAV2 | GRCh38.p7 | 9:133818146 | gaggtgggcagatca[C/G]gaggtcaggagatcg | 7410 |
rs2486332 | snp | A/G | 0.448836 | 0.15154 | intron-variant | VAV2 | GRCh38.p7 | 9:133818223 | tacaaaaaattagcc[A/G]ggcatggtggcgggc | 7410 |
rs2486333 | snp | A/G | 0.361053 | 0.22398 | intron-variant | VAV2 | GRCh38.p7 | 9:133905329 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7410 |
rs2486334 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | VAV2 | GRCh38.p7 | 9:133822272 | CGCCGCACTGGCCCC[A/G]GGCTGTCTGATGCTG | 7410 |
rs2486335 | snp | A/G | 0.243061 | 0.249904 | intron-variant | VAV2 | GRCh38.p7 | 9:133824156 | ATCCCAACGAGCTGC[A/G]GTCTCCACAGCCAGC | 7410 |
rs2486336 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | VAV2 | GRCh38.p7 | 9:133824214 | TAACAGGGAAGGTGC[A/G]GACAGGGAGCTCCCG | 7410 |
rs2486337 | snp | A/G | 0.250732 | 0.249999 | intron-variant | VAV2 | GRCh38.p7 | 9:133824680 | GCAGGGGCCCACAAC[A/G]GGGTCCCAGGTCCCA | 7410 |
rs2486338 | snp | C/G | 0.278399 | 0.248382 | intron-variant | VAV2 | GRCh38.p7 | 9:133824934 | GCGTCTTGACAGAGG[C/G]ACCCTCCGGGGACGC | 7410 |
rs2486339 | snp | A/G | 0.273587 | 0.248885 | intron-variant | VAV2 | GRCh38.p7 | 9:133824942 | ACAGAGGGACCCTCC[A/G]GGGACGCTGGCTTCA | 7410 |
rs2486340 | snp | A/G | 0.141258 | 0.225111 | intron-variant | VAV2 | GRCh38.p7 | 9:133825160 | AGGAGACAATGCCAC[A/G]GTCCAGCCAGGTGTC | 7410 |
rs2486341 | snp | A/C | 0.158962 | 0.232835 | intron-variant | VAV2 | GRCh38.p7 | 9:133825378 | ATTCCGGCCTCCTTC[A/C]GACCAGGGCAGGCTT | 7410 |
rs2486342 | snp | C/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133827204 | GCTGACCACTGAGCA[C/T]GGGCATCGCCAGCTA | 7410 |
rs2486343 | snp | C/T | 0.295854 | 0.245759 | intron-variant | VAV2 | GRCh38.p7 | 9:133827221 | GGCATCGCCAGCTAC[C/T]GCTGTGCCCACTGGG | 7410 |
rs2486344 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133827539 | GGCTGACCACTGAGC[A/G]CGGGCATCGCCAGCT | 7410 |
rs2486345 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133827540 | GCTGACCACTGAGCA[C/G]GGGCATCGCCAGCTA | 7410 |
rs2486348 | snp | C/G | 0.204803 | 0.245881 | intron-variant | VAV2 | GRCh38.p7 | 9:133832186 | TAACCCCCTAATCAC[C/G]GTGCACCCCTTGGGC | 7410 |
rs2486349 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | VAV2 | GRCh38.p7 | 9:133842757 | GCGGAGGCCATAGTG[A/G]GGAGAAAGAGAACAG | 7410 |
rs2486350 | snp | A/G | 0.434976 | 0.168179 | intron-variant | VAV2 | GRCh38.p7 | 9:133848560 | AAGGCTGGAGAAAGC[A/G]ACCAGCAAGGGCACC | 7410 |
rs2486351 | snp | C/T | 0.434253 | 0.168969 | intron-variant | VAV2 | GRCh38.p7 | 9:133851401 | TTTGAATCCTCATAA[C/T]AATCCAGTAACTCCA | 7410 |
rs2486352 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | VAV2 | GRCh38.p7 | 9:133851423 | GTAACTCCAAAGGGC[C/T]GGTGAGGACACTGAG | 7410 |
rs2486353 | snp | C/T | 0.453209 | 0.145623 | intron-variant | VAV2 | GRCh38.p7 | 9:133889014 | CCGCGTCCCCGTCCC[C/T]GGGGAAGCCTCACTT | 7410 |
rs2486354 | snp | C/T | 0.464947 | 0.127663 | intron-variant | VAV2 | GRCh38.p7 | 9:133889071 | ATGGCCTGAGGCAGG[C/T]CCGGCAGGGATCTGG | 7410 |
rs2486356 | snp | C/T | 0.263809 | 0.249618 | intron-variant | VAV2 | GRCh38.p7 | 9:133927369 | TTAGGCTCCTACCTC[C/T]ACTGATGTAGTAGGC | 7410 |
rs2486357 | snp | A/T | 0.265453 | 0.249522 | intron-variant | VAV2 | GRCh38.p7 | 9:133929011 | ACCCAGCCCATGAAA[A/T]CAGGCAGCGGCACCA | 7410 |
rs2486358 | snp | A/C | 0.188946 | 0.24243 | intron-variant | VAV2 | GRCh38.p7 | 9:133898622 | ataaataaaaaGATC[A/C]TTTTTAATCCCCTCA | 7410 |
rs2486359 | snp | A/G | 0.187685 | 0.242109 | intron-variant | VAV2 | GRCh38.p7 | 9:133898796 | GGCCGTGTCGGATCC[A/G]GGGAGGATGCAGACC | 7410 |
rs2486360 | snp | A/G | 0.182933 | 0.240836 | intron-variant | VAV2 | GRCh38.p7 | 9:133898805 | GGATCCAGGGAGGAT[A/G]CAGACCCTGCCtttt | 7410 |
rs2488551 | snp | C/G | 0.360842 | 0.224085 | intron-variant | VAV2 | GRCh38.p7 | 9:133821368 | GGGGAGGCAGCGAGG[C/G]AAACTAGGGTTGTCT | 7410 |
rs2488552 | snp | A/G | 0.488424 | 0.0751925 | intron-variant | VAV2 | GRCh38.p7 | 9:133803882 | TTTTCTACTGGGCTC[A/G]TGCCTCTCACCTTCC | 7410 |
rs2488555 | snp | A/G | 0.046775 | 0.145601 | intron-variant | VAV2 | GRCh38.p7 | 9:133825446 | ACGGCCCCACGAGAA[A/G]CAAGCAAATGAATCC | 7410 |
rs2488556 | snp | A/G | 0.272241 | 0.249009 | intron-variant | VAV2 | GRCh38.p7 | 9:133824920 | TCCCTCTGTCAAGAC[A/G]CTTCCAGTTGCATCT | 7410 |
rs2488557 | snp | A/G | 0.276534 | 0.248588 | intron-variant | VAV2 | GRCh38.p7 | 9:133824476 | GCCAGGCCAGTCACT[A/G]CCTTGTTTTGGGCTG | 7410 |
rs2488558 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | VAV2 | GRCh38.p7 | 9:133770745 | CTGACCAGCACGGAC[A/G]CTGACTGCAACAGCC | 7410 |
rs2488559 | snp | A/G | 0.339656 | 0.233371 | intron-variant | VAV2 | GRCh38.p7 | 9:133775104 | GAGGACAGTGTCTGA[A/G]GGGTGCCCAGCCCTC | 7410 |
rs2488560 | snp | A/G | 0.084364 | 0.187256 | intron-variant | VAV2 | GRCh38.p7 | 9:133775320 | GGGGTGACTGTGGCC[A/G]CCAGCCAGTCCCACA | 7410 |
rs2488561 | snp | C/T | 0.499933 | 0.00579035 | intron-variant | VAV2 | GRCh38.p7 | 9:133786507 | CCTGCGCTCATCCTT[C/T]CTGGGATCCTGCCCC | 7410 |
rs2488562 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | VAV2 | GRCh38.p7 | 9:133785384 | CGGGCTGGCGGCTTG[G/T]CACCTGTTTTTGAAG | 7410 |
rs2488563 | snp | A/G | 0.172674 | 0.237741 | intron-variant | VAV2 | GRCh38.p7 | 9:133783413 | CGGGCCTCGGGCACC[A/G]TCTCCCACGGGGCAG | 7410 |
rs2492052 | snp | C/T | 0.182933 | 0.240836 | intron-variant | VAV2 | GRCh38.p7 | 9:133898729 | TCATGAGGCCAGGCC[C/T]GAGCTGGTGCTGTGG | 7410 |
rs2492053 | snp | C/G | 0.182933 | 0.240836 | intron-variant | VAV2 | GRCh38.p7 | 9:133898787 | GCCACCACAGGCCGT[C/G]TCGGATCCAGGGAGG | 7410 |
rs2492054 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | VAV2 | GRCh38.p7 | 9:133914542 | CTGGTGACCAAGGGC[A/G]GTGGGGATGGGGTGG | 7410 |
rs2492055 | snp | A/G | 0.246769 | 0.249979 | intron-variant | VAV2 | GRCh38.p7 | 9:133915853 | ACACAACGCACACAC[A/G]CACGATGTACATGTA | 7410 |
rs2492056 | snp | G/T | 0.133777 | 0.221342 | intron-variant | VAV2 | GRCh38.p7 | 9:133925526 | cctggtcACAGTAAT[G/T]TTTTTTAAAGATTGA | 7410 |
rs2492057 | snp | G/T | 0.248471 | 0.249995 | intron-variant | VAV2 | GRCh38.p7 | 9:133925616 | GAATCTGCATGTTTC[G/T]CCACTGCCCTTGCTG | 7410 |
rs2492058 | snp | A/G | 0.248188 | 0.249993 | intron-variant | VAV2 | GRCh38.p7 | 9:133925656 | TGGGAAGCCCAGCAA[A/G]TTCACAGCCACACAC | 7410 |
rs2492059 | snp | G/T | 0.264906 | 0.249555 | intron-variant | VAV2 | GRCh38.p7 | 9:133929260 | ACCTGAGCCCTCAAG[G/T]TCAAGTCCGGACAGT | 7410 |
rs2492060 | snp | C/T | 0.444444 | 0.157135 | intron-variant | VAV2 | GRCh38.p7 | 9:133940688 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 7410 |
rs2492062 | snp | A/G | 0.147321 | 0.227941 | intron-variant | VAV2 | GRCh38.p7 | 9:133969864 | GTGTCCCTGTAGTGC[A/G]GACACAGTGGAGCTT | 7410 |
rs2492063 | snp | C/T | 0.289424 | 0.246872 | intron-variant | VAV2 | GRCh38.p7 | 9:133970594 | CTGCAGAGATGGAGG[C/T]GGCTCCTTCCCTGGG | 7410 |
rs2492064 | snp | A/T | 0.122064 | 0.214785 | intron-variant | VAV2 | GRCh38.p7 | 9:133976107 | AGCTACTCGGGAGGC[A/T]GAGGCAGAGAATTGC | 7410 |
rs2502733 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | VAV2 | GRCh38.p7 | 9:133849080 | AAAACAAACCAAGGC[C/T]GCCTCTTCAGCAACT | 7410 |
rs2502748 | snp | G/T | 0.20511 | 0.245937 | intron-variant | VAV2 | GRCh38.p7 | 9:133832413 | CAGAGGGAAGTCCCT[G/T]AGGGATAAGGCCCCA | 7410 |
rs2502749 | snp | C/T | 0.2768 | 0.248559 | intron-variant | VAV2 | GRCh38.p7 | 9:133825247 | AGACGGGGCGTTTCT[C/T]AAGGCGGGTGATGGC | 7410 |
rs2502750 | snp | C/T | 0.294064 | 0.246086 | intron-variant | VAV2 | GRCh38.p7 | 9:133824373 | GTTTTAGGAGGGTCC[C/T]GGTCTCTGCTGTGTC | 7410 |
rs2502751 | snp | C/T | 0.285257 | 0.247501 | intron-variant | VAV2 | GRCh38.p7 | 9:133822838 | ACATTCCCCTGGGCC[C/T]AGTCCTTGTGACCTG | 7410 |
rs2502752 | snp | A/G | 0.364193 | 0.222396 | intron-variant | VAV2 | GRCh38.p7 | 9:133820793 | CTCAGTGGGTCTCAT[A/G]GTATACCCCTCCTCC | 7410 |
rs2502753 | snp | A/C/G | 0.0193772 | 0.0965046 | intron-variant | VAV2 | GRCh38.p7 | 9:133816948 | aatggcttaatcagt[A/C/G]ttgtagaagaacaaa | 7410 |
rs2502754 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | VAV2 | GRCh38.p7 | 9:133784905 | GTCTTCTCACCACGC[C/T]GCCGCCATCCGCGTC | 7410 |
rs2502755 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | VAV2 | GRCh38.p7 | 9:133782566 | CATTTTGAGCTGTGA[C/T]TTTAGATCAATGGTT | 7410 |
rs2502756 | snp | C/T | 0.0314385 | 0.121371 | intron-variant, utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133782254 | AAGGTAATGTTTACT[C/T]ATCAAAAATTTGGAG | 7410 |
rs2502764 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | VAV2 | GRCh38.p7 | 9:133853768 | GGCTGTCCTGTCTGG[A/G]CAGTGTTGGCATGGG | 7410 |
rs2502765 | snp | A/C | 0.434253 | 0.168969 | intron-variant | VAV2 | GRCh38.p7 | 9:133851623 | ATTTCACATGAATAT[A/C]ACGCGATTGGTCTCA | 7410 |
rs2506685 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | VAV2 | GRCh38.p7 | 9:133976723 | AGTCCCACGTGATTC[C/T]CTTAAAACGTCCAGA | 7410 |
rs2506686 | snp | G/T | 0.370568 | 0.219005 | intron-variant | VAV2 | GRCh38.p7 | 9:133970796 | GGAGTGGCCTGCTAG[G/T]TCAGGGCTGCCCTGC | 7410 |
rs2510232 | snp | C/T | 0.235854 | 0.249599 | intron-variant | VAV2 | GRCh38.p7 | 9:133783361 | GCGTCTGGTGTCTGC[C/T]CTGGGGCACGTGAGC | 7410 |
rs2510233 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | VAV2 | GRCh38.p7 | 9:133840252 | GCGGTGCAGTGGGAA[A/G]CTCTGCTTCCCGAAG | 7410 |
rs2510236 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | VAV2 | GRCh38.p7 | 9:133832477 | GAGCCTCAGTTTCCT[A/C]CCCCCTTACAGGGTT | 7410 |
rs2510237 | snp | C/T | 0.140919 | 0.224948 | intron-variant | VAV2 | GRCh38.p7 | 9:133833490 | CCCAGGCAGCAAGGA[C/T]GCCCGAAGGCACCAT | 7410 |
rs2510238 | snp | A/G | 0.35894 | 0.225016 | intron-variant | VAV2 | GRCh38.p7 | 9:133834107 | TCCCACTCAGCACGG[A/G]AGCCCACACCATGAC | 7410 |
rs2510239 | snp | A/G | 0.493881 | 0.054972 | intron-variant | VAV2 | GRCh38.p7 | 9:133785183 | CTCCATTTCACCAGA[A/G]GAAACGGTCAGAGAG | 7410 |
rs2510242 | snp | G/T | 0.031825 | 0.122064 | intron-variant | VAV2 | GRCh38.p7 | 9:133786355 | GTGAGCTCTCCTGTG[G/T]GTGCTCTCCTGTGGG | 7410 |
rs2510243 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133772354 | AGAGGCTCCTGGTAC[C/T]GAAAAGCAAATGAGC | 7410 |
rs2510244 | snp | C/T | 0.41408 | 0.188621 | intron-variant | VAV2 | GRCh38.p7 | 9:133772120 | GCAGCAAACACAGAA[C/T]GAGCCTGGCTGCCAA | 7410 |
rs2510246 | snp | A/G | 0.462565 | 0.13159 | intron-variant | VAV2 | GRCh38.p7 | 9:133807371 | CTGCTGCTGTTGCCC[A/G]CCCTCTCAAGGTCAC | 7410 |
rs2510249 | snp | A/G | 0.242488 | 0.249887 | intron-variant | VAV2 | GRCh38.p7 | 9:133813327 | AGGGAGGCGAGGCAG[A/G]GACAGAAGCCGGGGC | 7410 |
rs2510250 | snp | A/G | 0.26326 | 0.249648 | intron-variant | VAV2 | GRCh38.p7 | 9:133855363 | TGGTTTTGCCTTCCC[A/G]AATCACCTACAAGGT | 7410 |
rs2510251 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | VAV2 | GRCh38.p7 | 9:133854238 | GATGAGTGCATGTAT[A/G]TGTGCAGGTGCACAT | 7410 |
rs2510252 | snp | A/G | 0.387642 | 0.208697 | intron-variant | VAV2 | GRCh38.p7 | 9:133854133 | GCAGGTGCAAGGGGT[A/G]TGTGTGTGCAGGTGC | 7410 |
rs2510253 | snp | G/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133854122 | gggtgtgtgtgtgca[G/T]gtgcaaggggtatgt | 7410 |
rs2510254 | snp | C/T | 0.407674 | 0.194008 | intron-variant | VAV2 | GRCh38.p7 | 9:133853574 | GATGCAGACTCCGCT[C/T]GGCCGTTCCCTGCCC | 7410 |
rs2510255 | snp | A/G | 0.144969 | 0.226867 | intron-variant | VAV2 | GRCh38.p7 | 9:133776483 | AGGTGCTGCCGCTCC[A/G]GTGAGCAGGTAGGGC | 7410 |
rs2510256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV2 | GRCh38.p7 | 9:133820831 | AAGTCTCCTGGGAGT[A/G]CAGGGCAGTGACAGG | 7410 |
rs2510258 | snp | A/G | 0.2462 | 0.249971 | intron-variant | VAV2 | GRCh38.p7 | 9:133845428 | CCAGAATGGGGGGCC[A/G]CACTGGGGGTTCTCT | 7410 |
rs2510259 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | VAV2 | GRCh38.p7 | 9:133778498 | CAGGAGGGCCTCTCC[C/T]GGGAAGGGACGCTGC | 7410 |
rs2510260 | snp | A/C | 0.0141837 | 0.08301 | intron-variant | VAV2 | GRCh38.p7 | 9:133829549 | CAGCGCAAGCACCAC[A/C]AAACGTAGGCTGCCC | 7410 |
rs2510261 | snp | C/T | 0.122411 | 0.214991 | intron-variant | VAV2 | GRCh38.p7 | 9:133831682 | GTCCCGGAGCCCTCC[C/T]GTGCTGACTGTCCAG | 7410 |
rs2510262 | snp | A/G | 0.269267 | 0.249256 | intron-variant | VAV2 | GRCh38.p7 | 9:133801361 | CAGAAGTCACGTCAC[A/G]TCTCTGAGCCTCAGG | 7410 |
rs2510264 | snp | C/T | 0.342806 | 0.232136 | intron-variant, utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133781931 | AAAAATTCAAAACCA[C/T]ACAGAGATGGGGTGG | 7410 |
rs2510265 | snp | C/T | 0.222035 | 0.248431 | intron-variant | VAV2 | GRCh38.p7 | 9:133799048 | ACAGGCCCAGCTGCC[C/T]GCCCCGAGCCCCAGG | 7410 |
rs2519096 | snp | C/T | 0.152001 | 0.229992 | intron-variant | VAV2 | GRCh38.p7 | 9:133929924 | TCTTCAGAACCCTTT[C/T]TTTAAGCAAAATGTC | 7410 |
rs2519097 | snp | C/T | 0.254944 | 0.249951 | intron-variant | VAV2 | GRCh38.p7 | 9:133930439 | CCTCCGGCATCCTCA[C/T]TGCCTCTTGGCCTCT | 7410 |
rs2519098 | snp | C/T | 0.337614 | 0.234145 | intron-variant | VAV2 | GRCh38.p7 | 9:133933248 | AAGCTCCAGAGTTTT[C/T]ACTTTCTCACTCCTC | 7410 |
rs2519099 | snp | C/T | 0.340108 | 0.233197 | intron-variant | VAV2 | GRCh38.p7 | 9:133933981 | gaatggatggaagga[C/T]gggtgaatgggtggg | 7410 |
rs2519100 | snp | C/G | 0.496483 | 0.0417852 | intron-variant | VAV2 | GRCh38.p7 | 9:133936650 | GGTGGGGGGCGGCAG[C/G]AGCAGCAACCTGCAC | 7410 |
rs2519101 | snp | C/G | 0.265453 | 0.249522 | intron-variant | VAV2 | GRCh38.p7 | 9:133937202 | TACATGTGAGACTGT[C/G]TGTGTGTGAATGTGT | 7410 |
rs2519102 | snp | G/T | 0.377582 | 0.214995 | intron-variant | VAV2 | GRCh38.p7 | 9:133940172 | GCCTGGTTTTCTACC[G/T]CCACCTGCCTCACGG | 7410 |
rs2519103 | snp | G/T | 0.425894 | 0.177655 | intron-variant | VAV2 | GRCh38.p7 | 9:133940498 | CCCTGGGAGCGGAGG[G/T]TCCCCCAGCCAGGAC | 7410 |
rs2519104 | snp | A/G | 0.42574 | 0.177808 | intron-variant | VAV2 | GRCh38.p7 | 9:133940851 | acatggacaccacac[A/G]gttatcttatctata | 7410 |
rs2519105 | snp | A/G | 0.432797 | 0.170544 | intron-variant | VAV2 | GRCh38.p7 | 9:133941729 | CTGCCTGAGCCTCCC[A/G]AGTAGCTGGGATTAC | 7410 |
rs2519106 | snp | A/C | 0.373397 | 0.217424 | intron-variant | VAV2 | GRCh38.p7 | 9:133942161 | tattttaccacaata[A/C]aaagaTTAATTAGAA | 7410 |
rs2519107 | snp | A/T | 0.426813 | 0.17674 | intron-variant | VAV2 | GRCh38.p7 | 9:133942335 | ACGGGCTCTCCTCCG[A/T]GGCCCCACGAAGGAG | 7410 |
rs2519108 | snp | A/G | 0.424037 | 0.179474 | intron-variant | VAV2 | GRCh38.p7 | 9:133942518 | TACGCCCTCTCGCTC[A/G]TCTGCGCGGCTGCAT | 7410 |
rs2519109 | snp | A/G | 0.426507 | 0.177046 | intron-variant | VAV2 | GRCh38.p7 | 9:133942648 | TAGAGTTAATTACAC[A/G]GATCCCAACCATAAT | 7410 |
rs2519110 | snp | A/G | 0.409212 | 0.192748 | intron-variant | VAV2 | GRCh38.p7 | 9:133943994 | ACAGACAGGAGAGGC[A/G]GCGCAGGGCCGGAGA | 7410 |
rs2519111 | snp | C/G | 0.40853 | 0.193309 | intron-variant | VAV2 | GRCh38.p7 | 9:133943996 | AGACAGGAGAGGCGG[C/G]GCAGGGCCGGAGAGC | 7410 |
rs2519112 | snp | A/G | 0.370162 | 0.219229 | intron-variant | VAV2 | GRCh38.p7 | 9:133946625 | GGCTGCTCTGCTTCC[A/G]GCTGGAGTGGTGCTG | 7410 |
rs2519113 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | VAV2 | GRCh38.p7 | 9:133957842 | AAGAAGTAGACATGG[A/G]AGACTCCATTTTGTT | 7410 |
rs2519114 | snp | A/C | 0.44306 | 0.158832 | intron-variant | VAV2 | GRCh38.p7 | 9:133958659 | ttctctatactttgt[A/C]tctgtgtctttttct | 7410 |
rs2519115 | snp | C/G | 0.426201 | 0.177351 | intron-variant | VAV2 | GRCh38.p7 | 9:133890562 | ATCAAGCATCTGCCT[C/G]TCATGGACAAAGGGG | 7410 |
rs2519132 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | VAV2 | GRCh38.p7 | 9:133981084 | AGGGCCTCCTGGGTT[G/T]GACTGGGCGAAGATG | 7410 |
rs2519133 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV2 | GRCh38.p7 | 9:133975267 | GCACTGAGCGAGGAT[A/G]TGGGTTTGTGTCCAG | 7410 |
rs2519134 | snp | G/T | 0.273318 | 0.24891 | intron-variant | VAV2 | GRCh38.p7 | 9:133975169 | CCTTTCCTAGTAAGG[G/T]GATGGGTTCTGCCTC | 7410 |
rs2519135 | snp | A/G | 0.275464 | 0.2487 | intron-variant | VAV2 | GRCh38.p7 | 9:133975167 | TTTCCTAGTAAGGGG[A/G]TGGGTTCTGCCTCGG | 7410 |
rs2519136 | snp | A/G | 0.486266 | 0.0817214 | intron-variant | VAV2 | GRCh38.p7 | 9:133973741 | CGTGGGTAGCCACAC[A/G]CTGGCAATGTCCCAG | 7410 |
rs2519138 | snp | A/G | 0.183886 | 0.241099 | intron-variant | VAV2 | GRCh38.p7 | 9:133970582 | GCCACCTCCATCTCT[A/G]CAGCCCCACATGTGT | 7410 |
rs2519139 | snp | A/G | 0.424348 | 0.179172 | intron-variant | VAV2 | GRCh38.p7 | 9:133970510 | GCCGTGGACAGCCTC[A/G]TGATCGCCACTGCCA | 7410 |
rs2519140 | snp | A/G | 0.433382 | 0.169915 | intron-variant | VAV2 | GRCh38.p7 | 9:133970493 | GATCGCCACTGCCAC[A/G]CCTCTGTGGGCTCCT | 7410 |
rs2519766 | snp | A/G | 0.426813 | 0.17674 | intron-variant | VAV2 | GRCh38.p7 | 9:133890468 | GCAGAAATGGGAAAA[A/G]TGCCGAGGGTCAAGG | 7410 |
rs2519767 | snp | A/C | 0.426507 | 0.177046 | intron-variant | VAV2 | GRCh38.p7 | 9:133890525 | AAGACGACCGCCCCC[A/C]ACCACCCCCTAGAGT | 7410 |
rs2519768 | snp | C/T | 0.42666 | 0.176893 | intron-variant | VAV2 | GRCh38.p7 | 9:133890636 | TGCAGAAAGGAATGG[C/T]CCCAGAACCACGCTC | 7410 |
rs2519769 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | VAV2 | GRCh38.p7 | 9:133890891 | TGGGCACTACGGAGG[A/G]GCATCTCTCTTGCTA | 7410 |
rs2519770 | snp | A/G | 0.43088 | 0.172575 | intron-variant | VAV2 | GRCh38.p7 | 9:133891173 | AGGGTGCAGGGGGCT[A/G]CCAGGGCCCGGCACT | 7410 |
rs2519771 | snp | C/T | 0.429837 | 0.173662 | intron-variant | VAV2 | GRCh38.p7 | 9:133891194 | GCCCGGCACTCACGC[C/T]ACCCTCAGGAACACA | 7410 |
rs2519772 | snp | G/T | 0.431916 | 0.171483 | intron-variant | VAV2 | GRCh38.p7 | 9:133892288 | TGCATGGGGCTGTGC[G/T]GCTAGGAAGTGAGGC | 7410 |
rs2519773 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | VAV2 | GRCh38.p7 | 9:133892507 | AGTCACTTGGCCAAG[A/G]TCATCCCAGGGGTCA | 7410 |
rs2519774 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | VAV2 | GRCh38.p7 | 9:133892594 | GCCGAGCACCTAACC[C/T]GCCTGGCCGTCCCTC | 7410 |
rs2519775 | snp | C/G | 0.421368 | 0.182025 | intron-variant | VAV2 | GRCh38.p7 | 9:133894064 | TGGCTGAGAATCCAT[C/G]CCCCACTCCCCGCCT | 7410 |
rs2519776 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV2 | GRCh38.p7 | 9:133894099 | TGCCCGTCAGAATTC[A/G]GGGAAGCTGCACGGG | 7410 |
rs2519777 | snp | A/C | 0.420892 | 0.182472 | intron-variant | VAV2 | GRCh38.p7 | 9:133894386 | GAGGCGGCTGGGTGC[A/C]TCCATCCACAAAACC | 7410 |
rs2519778 | snp | C/T | 0.420096 | 0.183214 | intron-variant | VAV2 | GRCh38.p7 | 9:133894465 | AAAGGTGGAAACCGC[C/T]TTTACGCCCTCTGAG | 7410 |
rs2519779 | snp | G/T | 0.420255 | 0.183066 | intron-variant | VAV2 | GRCh38.p7 | 9:133894543 | GCACAAGGCGGCTGT[G/T]GGGAAATTTTGCCAC | 7410 |
rs2519780 | snp | A/G | 0.424851 | 0.188186 | intron-variant | VAV2 | GRCh38.p7 | 9:133895023 | TTCTGAAGATCGCGT[A/G]GGGGGCGTCCGGAGA | 7410 |
rs2519781 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | VAV2 | GRCh38.p7 | 9:133897522 | TCCCAGGAGGGTGAG[C/G]TCCTTCCTGTCTCCC | 7410 |
rs2519782 | snp | A/T | 0.197703 | 0.244469 | intron-variant | VAV2 | GRCh38.p7 | 9:133898437 | CTACTAAAAAAAAAA[A/T]ACAAAAATCAGCCAG | 7410 |
rs2519783 | snp | A/G | 0.372592 | 0.217879 | intron-variant | VAV2 | GRCh38.p7 | 9:133898549 | CAGTGAGCCGAGATC[A/G]TGCCACTGTACTCCA | 7410 |
rs2519784 | snp | C/T | 0.184285 | 0.241436 | intron-variant | VAV2 | GRCh38.p7 | 9:133899262 | GAGACCCATGGGGAG[C/T]TGGGACTCCTCAggc | 7410 |
rs2519785 | snp | A/G | 0.436408 | 0.16659 | intron-variant | VAV2 | GRCh38.p7 | 9:133901215 | TCATGTAAAAGCACC[A/G]CTCCGGGGGCCCAGT | 7410 |
rs2519786 | snp | C/G | 0.193028 | 0.243422 | intron-variant | VAV2 | GRCh38.p7 | 9:133901499 | AGAGCCATGGCACCA[C/G]CTCGAGCCTGGTCTC | 7410 |
rs2519787 | snp | C/T | 0.367091 | 0.220884 | intron-variant | VAV2 | GRCh38.p7 | 9:133901529 | CATGAGGCCTAGAAG[C/T]TTCCGTGGGTGCCAC | 7410 |
rs2519788 | snp | G/T | 0.344592 | 0.231414 | intron-variant | VAV2 | GRCh38.p7 | 9:133901710 | ACTGGGCTGGGCCCA[G/T]CCCTCCTGGGGTATT | 7410 |
rs2519789 | snp | C/G | 0.328382 | 0.237395 | intron-variant | VAV2 | GRCh38.p7 | 9:133904319 | GACATTAAAAAGACA[C/G]AGAAGAATCCCAAGT | 7410 |
rs2519790 | snp | C/G | 0.400504 | 0.199621 | intron-variant | VAV2 | GRCh38.p7 | 9:133904415 | TGAGTTCATGTCCTC[C/G]AGGGTCCCGTGAAAT | 7410 |
rs2519791 | snp | C/G | 0.477004 | 0.104734 | intron-variant | VAV2 | GRCh38.p7 | 9:133905404 | TTGTGCCACTGCACT[C/G]CAGCCTGGGTGACAG | 7410 |
rs2519792 | snp | A/G | 0.417521 | 0.185571 | intron-variant | VAV2 | GRCh38.p7 | 9:133905719 | CCACCTCTGTAGTGG[A/G]TCACTGGGGCTGCAG | 7410 |
rs2519793 | snp | C/G | 0.079617 | 0.182947 | intron-variant | VAV2 | GRCh38.p7 | 9:133910019 | CCACACGagctatgc[C/G]aggccatgtgactag | 7410 |
rs2519794 | snp | C/G | 0.333261 | 0.235728 | intron-variant | VAV2 | GRCh38.p7 | 9:133910428 | GCACCGTGCGGTGGG[C/G]TCTCTCATGTAACCG | 7410 |
rs2519795 | snp | C/G | 0.0861826 | 0.188849 | intron-variant | VAV2 | GRCh38.p7 | 9:133910932 | CACAGTCCCGCAGAC[C/G]GCAAGCCCATCCCAG | 7410 |
rs2519796 | snp | C/T | 0.443598 | 0.158176 | intron-variant | VAV2 | GRCh38.p7 | 9:133960211 | CGATGCCTTTGGGAA[C/T]GCGTTGTCTTGCTGG | 7410 |
rs2519797 | snp | A/G | 0.44306 | 0.158832 | intron-variant | VAV2 | GRCh38.p7 | 9:133959778 | CAGGGCCTCATCCCT[A/G]TGCCTCTCTCCTCTT | 7410 |
rs2519798 | snp | C/T | 0.444799 | 0.156695 | intron-variant | VAV2 | GRCh38.p7 | 9:133959730 | GCTGGTCATTGGATT[C/T]GGGGCCCACCCTAAC | 7410 |
rs2519799 | snp | A/G | 0.373196 | 0.217538 | intron-variant | VAV2 | GRCh38.p7 | 9:133945735 | CTGCCTGTTGGTGAC[A/G]ATCTACATGGATGGG | 7410 |
rs2519802 | snp | C/T | 0.395087 | 0.203592 | intron-variant | VAV2 | GRCh38.p7 | 9:133940731 | GGAGTGTCATTACTG[C/T]AGTTAATCTCGAGTG | 7410 |
rs2519803 | snp | C/T | 0.425586 | 0.17796 | intron-variant | VAV2 | GRCh38.p7 | 9:133940667 | ACACACACACGCACG[C/T]GGACAGAGAGGGACT | 7410 |
rs2519804 | snp | C/T | 0.426047 | 0.177503 | intron-variant | VAV2 | GRCh38.p7 | 9:133940617 | TCTGTTGTCTATGAA[C/T]AGCAGCCGACCCCTG | 7410 |
rs2519805 | snp | C/G | 0.339203 | 0.233544 | intron-variant | VAV2 | GRCh38.p7 | 9:133939553 | GCCGCCCTGACCTAC[C/G]GTTACGGGGAGTGGC | 7410 |
rs2519806 | snp | A/G | 0.243919 | 0.249926 | intron-variant | VAV2 | GRCh38.p7 | 9:133938308 | TTCCTGATGGATTCG[A/G]GGCTGGACGCCGGAG | 7410 |
rs2519807 | snp | A/G | 0.441841 | 0.160303 | intron-variant | VAV2 | GRCh38.p7 | 9:133960986 | AGACCTGTGGTCACC[A/G]TTCCTCTCCAAGCAC | 7410 |
rs2519808 | snp | A/T | 0.26518 | 0.249539 | intron-variant | VAV2 | GRCh38.p7 | 9:133937169 | CACATACTTAGACAC[A/T]CAACTGGTATTTATG | 7410 |
rs2519809 | snp | C/T | 0.24449 | 0.249939 | intron-variant | VAV2 | GRCh38.p7 | 9:133936514 | GGCTCACGCCTGTAA[C/T]CTGAGCACTTTGGAA | 7410 |
rs2519810 | snp | C/T | 0.44306 | 0.158832 | intron-variant | VAV2 | GRCh38.p7 | 9:133958682 | aggtggaacgagaga[C/T]ttggaaaagaaaaag | 7410 |
rs2519811 | snp | C/T | 0.442926 | 0.158996 | intron-variant | VAV2 | GRCh38.p7 | 9:133935605 | TCTCCGGGACAGGTG[C/T]TCTGGAAAAACAAAA | 7410 |
rs2519812 | snp | A/T | 0.33875 | 0.233717 | intron-variant | VAV2 | GRCh38.p7 | 9:133934279 | GGTCTGTGGTGTTTC[A/T]GATCTTGTCTGGGCT | 7410 |
rs2519813 | snp | C/T | 0.337386 | 0.23423 | intron-variant | VAV2 | GRCh38.p7 | 9:133934069 | cactcaccatccatc[C/T]atccatcaatcattc | 7410 |
rs2519815 | snp | C/T | 0.339429 | 0.233457 | intron-variant | VAV2 | GRCh38.p7 | 9:133933572 | CATCCATCCACCATC[C/T]ATCCATCCATCCACC | 7410 |
rs2519816 | snp | A/G | 0.247337 | 0.249986 | intron-variant | VAV2 | GRCh38.p7 | 9:133933528 | TCCACTCATCCATTC[A/G]TCCATCATTCATCCA | 7410 |
rs2519817 | snp | A/C | 0.337841 | 0.23406 | intron-variant | VAV2 | GRCh38.p7 | 9:133933371 | GCATATAATTTACCA[A/C]GTATTTAGTAAGCAC | 7410 |
rs2519818 | snp | C/T | 0.34101 | 0.232846 | intron-variant | VAV2 | GRCh38.p7 | 9:133932018 | TAGGGACTCTGATCT[C/T]ATTGCGAGCTGGGAC | 7410 |
rs2519821 | snp | A/C | 0.439502 | 0.163061 | intron-variant | VAV2 | GRCh38.p7 | 9:133957806 | acagatacagtgaca[A/C]tctgatctctcttgc | 7410 |
rs2519822 | snp | C/T | 0.432944 | 0.170387 | intron-variant | VAV2 | GRCh38.p7 | 9:133957097 | CACCAGAGGGTAGGC[C/T]TGCACAGAGTGAGGA | 7410 |
rs2519823 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV2 | GRCh38.p7 | 9:133973640 | TCAAAATAACACGAC[A/G]CTCTCCCTCCCAATT | 7410 |
rs2519824 | snp | A/G | 0.498964 | 0.02274 | intron-variant | VAV2 | GRCh38.p7 | 9:133987379 | AAACCCAAGGAGGCT[A/G]CCAAGGGGAGGGAGC | 7410 |
rs2519825 | snp | A/G | 0.309648 | 0.24278 | intron-variant | VAV2 | GRCh38.p7 | 9:133987545 | GGGAAGAGGCAGGGA[A/G]CACAGGGAGTTGAGG | 7410 |
rs2519990 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | VAV2 | GRCh38.p7 | 9:133906442 | CCCGCCCTGCCCACT[C/T]GCCCCACTGACAGCT | 7410 |
rs2519991 | snp | C/T | 0.10237 | 0.201756 | intron-variant | VAV2 | GRCh38.p7 | 9:133907871 | CCACCCCCTTTCCTT[C/T]ACCGCCCTCCCCCAG | 7410 |
rs2519992 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | VAV2 | GRCh38.p7 | 9:133907957 | CCCTCCCCCAGAGAG[C/T]GGAGGGTCTGAAGGC | 7410 |
rs2519993 | snp | C/T | 0.311614 | 0.242289 | intron-variant | VAV2 | GRCh38.p7 | 9:133903742 | CAGCGTCAGAAAAAA[C/T]TCTCAACAGGGGGAT | 7410 |
rs2519994 | snp | A/C | 0.405776 | 0.195535 | intron-variant | VAV2 | GRCh38.p7 | 9:133903792 | TCCCTGGAGGGCAGA[A/C]AAATCCACTTCGTCA | 7410 |
rs2519995 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | VAV2 | GRCh38.p7 | 9:133910791 | ATTGCACCACTGCAC[C/T]CCAGCCTGGGCGACA | 7410 |
rs2519996 | snp | C/T | 0.267636 | 0.249377 | intron-variant | VAV2 | GRCh38.p7 | 9:133904226 | TCTAAAGGGAACCAC[C/T]CTGCCACACACAGCT | 7410 |
rs2520002 | snp | C/T | 0.41325 | 0.18934 | intron-variant | VAV2 | GRCh38.p7 | 9:133772897 | CGTCCAGCCTACATG[C/T]GGGGTGTGCAGTAGG | 7410 |
rs2520003 | snp | C/T | 0.299411 | 0.245069 | intron-variant | VAV2 | GRCh38.p7 | 9:133788916 | CTGCCGGAGAGTGTC[C/T]AGGCGCACGGTGGCC | 7410 |
rs2789820 | snp | A/G | 0.435263 | 0.167862 | intron-variant | VAV2 | GRCh38.p7 | 9:133901661 | GAGGGGCTCCTGCCG[A/G]CCCGGCCTGGTGACT | 7410 |
rs2789821 | snp | A/G | 0.1652 | 0.235179 | intron-variant | VAV2 | GRCh38.p7 | 9:133902372 | CCTCCATGCAGACAC[A/G]GCTGCGGCCTTGGGG | 7410 |
rs2789822 | snp | A/G | 0.396 | 0.202938 | intron-variant | VAV2 | GRCh38.p7 | 9:133903715 | CTCACAAGCGTGGGC[A/G]TCACTGAAAAACAGC | 7410 |
rs2789823 | snp | A/G | 0.372391 | 0.217992 | intron-variant | VAV2 | GRCh38.p7 | 9:133904766 | GAGTCAGTGCTGAGG[A/G]CCCCGTGAAGCTCAC | 7410 |
rs2789824 | snp | C/T | 0.103794 | 0.20279 | intron-variant | VAV2 | GRCh38.p7 | 9:133908857 | CTGCAGTTCTGAAAA[C/T]GTGTGGGGACCCAGG | 7410 |
rs2789825 | snp | C/T | 0.103438 | 0.202533 | intron-variant | VAV2 | GRCh38.p7 | 9:133909095 | AACTCCAGGCACCCC[C/T]AGCAATCGCGAGGAA | 7410 |
rs2789826 | snp | C/G | 0.103438 | 0.202533 | intron-variant | VAV2 | GRCh38.p7 | 9:133909342 | CCTGGAGCTCAGCAG[C/G]AGGTTCAAAACTCAG | 7410 |
rs2789827 | snp | A/T | 0.097727 | 0.198275 | intron-variant | VAV2 | GRCh38.p7 | 9:133909940 | GCTGGGGGCCTCCCA[A/T]CCTCCATCCTCCCCT | 7410 |
rs2789828 | snp | C/T | 0.330016 | 0.236849 | intron-variant | VAV2 | GRCh38.p7 | 9:133910478 | gatgaggtgccaagg[C/T]tcagtgagtcacttc | 7410 |
rs2789829 | snp | A/G | 0.123452 | 0.215605 | intron-variant | VAV2 | GRCh38.p7 | 9:133911052 | CCAGCTCCTGGCCAG[A/G]CTACATGGGCTGCAG | 7410 |
rs2789831 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | VAV2 | GRCh38.p7 | 9:133914981 | GGCATCAAACCCAGG[A/G]CAGCTCGCACGGGGG | 7410 |
rs2789832 | snp | A/C | 0.32885 | 0.23724 | intron-variant | VAV2 | GRCh38.p7 | 9:133915751 | GCACACATACACACA[A/C]GATGCACACATACAC | 7410 |
rs2789833 | snp | C/G | 0.218151 | 0.247963 | intron-variant | VAV2 | GRCh38.p7 | 9:133916306 | GCAAGATGAATTGCC[C/G]GCGGAGCCTGTGACT | 7410 |
rs2789834 | snp | A/G | 0.218151 | 0.247963 | intron-variant | VAV2 | GRCh38.p7 | 9:133916369 | GGAAAGTTTCTCTCC[A/G]CGGGATAAAGCCCTC | 7410 |
rs2789835 | snp | C/G | 0.0898077 | 0.191933 | intron-variant | VAV2 | GRCh38.p7 | 9:133916984 | AAACCCGGAGCTTTG[C/G]GAACACTCAGCAAGG | 7410 |
rs2789840 | snp | C/T | 0.274969 | 0.258193 | intron-variant | VAV2 | GRCh38.p7 | 9:133925823 | CAAGAAATGACACTT[C/T]GTTATAATTAATTAC | 7410 |
rs2789841 | snp | C/T | 0.323908 | 0.238825 | intron-variant | VAV2 | GRCh38.p7 | 9:133929726 | CAGCAGGTGCACAGC[C/T]GACTCCCTCATCCTG | 7410 |
rs2789842 | snp | C/T | 0.254664 | 0.249956 | intron-variant | VAV2 | GRCh38.p7 | 9:133930466 | CTCTTCACTGCCACC[C/T]GGCCTCCTCTCTGCC | 7410 |
rs2789843 | snp | C/T | 0.340108 | 0.233197 | intron-variant | VAV2 | GRCh38.p7 | 9:133932591 | CGTTCATTTTTTCAC[C/T]GAGTCCTTTACAGCA | 7410 |
rs2789844 | snp | G/T | 0.245916 | 0.249967 | intron-variant | VAV2 | GRCh38.p7 | 9:133932709 | GCGTCCAGGTCTGAC[G/T]GAAGCTTTGCTCTCA | 7410 |
rs2789845 | snp | C/T | 0.347032 | 0.230401 | intron-variant | VAV2 | GRCh38.p7 | 9:133934793 | GGCCCTCCACCTCCA[C/T]AGTCGCGAGAGCCGA | 7410 |
rs2789846 | snp | C/G | 0.264358 | 0.249587 | intron-variant | VAV2 | GRCh38.p7 | 9:133937820 | TCAAACTCCCAGGCA[C/G]GTGCGCTGCTGCAGG | 7410 |
rs2789847 | snp | A/T | 0.228253 | 0.249052 | intron-variant | VAV2 | GRCh38.p7 | 9:133938686 | GTAGGCGCTTTCCCC[A/T]CCTCATCTCCCCAGC | 7410 |
rs2789848 | snp | A/G | 0.396364 | 0.202676 | intron-variant | VAV2 | GRCh38.p7 | 9:133941340 | ttgaactcaggaagc[A/G]gaggttgcagtgagc | 7410 |
rs2789849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV2 | GRCh38.p7 | 9:133941390 | tccagcctgggtgac[A/G]gagcgagactccgtc | 7410 |
rs2789850 | snp | C/T | 0.425894 | 0.177655 | intron-variant | VAV2 | GRCh38.p7 | 9:133942533 | ATCTGCGCGGCTGCA[C/T]GTGCTGCAGCTTCCA | 7410 |
rs2789851 | snp | C/G | 0.42666 | 0.176893 | intron-variant | VAV2 | GRCh38.p7 | 9:133942806 | TAAGAAGTCCTCCTG[C/G]TGCAGCTCTGGGCCC | 7410 |
rs2789852 | snp | C/T | 0.367503 | 0.220665 | intron-variant | VAV2 | GRCh38.p7 | 9:133943930 | GCCCACCTCCCCAGG[C/T]TCAGCTGCACTGTCC | 7410 |
rs2789853 | snp | C/T | 0.468148 | 0.122112 | intron-variant | VAV2 | GRCh38.p7 | 9:133888124 | CCTACAGGAGGTCCC[C/T]GCAGGACTCTCTTAC | 7410 |
rs2789854 | snp | A/C | 0.375 | 0.216506 | intron-variant | VAV2 | GRCh38.p7 | 9:133889763 | TTACACACACACACA[A/C]AAAATTTTTTTCTTC | 7410 |
rs2789857 | snp | C/T | 0.442249 | 0.159814 | intron-variant | VAV2 | GRCh38.p7 | 9:133958758 | TGGAGCCAACAAGGA[C/T]GCTGCAGAGCACAGC | 7410 |
rs2789858 | snp | A/G | 0.432944 | 0.170387 | intron-variant | VAV2 | GRCh38.p7 | 9:133959358 | GCTCCGGGCTTCCCC[A/G]ACGGTGACCTCCCCA | 7410 |
rs2789859 | snp | A/C | 0.441841 | 0.160303 | intron-variant | VAV2 | GRCh38.p7 | 9:133959418 | CTCCTTCCCAGGGTG[A/C]CCACCTCTCAAGCTG | 7410 |
rs2789860 | snp | C/G | 0.442791 | 0.15916 | intron-variant | VAV2 | GRCh38.p7 | 9:133959715 | AAGAGGCCATCCCAG[C/G]TTAGGGTGGGCCCCG | 7410 |
rs2789861 | snp | C/G | 0.444533 | 0.157025 | intron-variant | VAV2 | GRCh38.p7 | 9:133959728 | AGGTTAGGGTGGGCC[C/G]CGAATCCAATGACCA | 7410 |
rs2789862 | snp | C/T | 0.438386 | 0.164349 | intron-variant | VAV2 | GRCh38.p7 | 9:133959881 | CTCCCCTAGTGCCTC[C/T]GGAGGGAGGGGCTGC | 7410 |
rs2789863 | snp | C/T | 0.438806 | 0.163867 | intron-variant | VAV2 | GRCh38.p7 | 9:133987698 | GGGCGGCGGGTGGTA[C/T]CTTAAGGGTGCAAAC | 7410 |
rs2789864 | snp | C/T | 0.438526 | 0.164189 | intron-variant | VAV2 | GRCh38.p7 | 9:133987769 | AAGCTGCTCCAGACA[C/T]ACCCGATTTCTCGTT | 7410 |
rs2789865 | snp | C/G | 0.433236 | 0.170072 | intron-variant | VAV2 | GRCh38.p7 | 9:133988257 | GCCACCCCATGAAAA[C/G]AGACACACACCGTGA | 7410 |
rs2789866 | snp | C/G | 0.463343 | 0.130326 | intron-variant | VAV2 | GRCh38.p7 | 9:133991561 | GGCGGTGCCCGGGGC[C/G]AACCCAGCTCCCTcc | 7410 |
rs2789867 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | VAV2 | GRCh38.p7 | 9:133892450 | ACCCTTACCAGTGCA[C/T]ACACCTCTGTCTATA | 7410 |
rs2797825 | snp | A/G | 0.432651 | 0.170701 | intron-variant | VAV2 | GRCh38.p7 | 9:133764176 | GGTGTGTGCATGTCT[A/G]TGTTGGGGTGAGGGC | 7410 |
rs2797826 | snp | A/G | 0.422787 | 0.180679 | intron-variant | VAV2 | GRCh38.p7 | 9:133764277 | TGCCTGGGAGTAAGA[A/G]CAACCCAGAAAAACA | 7410 |
rs2810468 | snp | C/T | 0.420255 | 0.183066 | intron-variant | VAV2 | GRCh38.p7 | 9:133894633 | AGGAGGGGCCAGCCC[C/T]TTCCCCACCGTCTCA | 7410 |
rs2810469 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | VAV2 | GRCh38.p7 | 9:133894855 | ATGACGCTATGACCC[C/T]AGGCAGGGTCCAGAG | 7410 |
rs2810470 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | VAV2 | GRCh38.p7 | 9:133989561 | gtggtggagcgtgcc[C/G]gtagtcccagctact | 7410 |
rs2810471 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133989602 | aggcagcagaatcgc[C/T]tgaacccaggaggtg | 7410 |
rs2810472 | snp | C/T | 0.461481 | 0.133325 | intron-variant | VAV2 | GRCh38.p7 | 9:133895517 | agctctgattctcac[C/T]gcaacgtgCCAGCGG | 7410 |
rs2810473 | snp | C/T | 0.428786 | 0.174744 | intron-variant | VAV2 | GRCh38.p7 | 9:133895729 | ttagtggtggataca[C/T]ggccttgtgaataca | 7410 |
rs2810481 | snp | A/G | 0.193028 | 0.243422 | intron-variant | VAV2 | GRCh38.p7 | 9:133898195 | ACTGAGGCCGGGCGG[A/G]CACAGGTTGATCTAG | 7410 |
rs2810482 | snp | C/T | 0.192715 | 0.243348 | intron-variant | VAV2 | GRCh38.p7 | 9:133898202 | CCGGGCGGGCACAGG[C/T]TGATCTAGTGTCACC | 7410 |
rs2810483 | snp | A/G | 0.19646 | 0.2442 | intron-variant | VAV2 | GRCh38.p7 | 9:133898497 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATCACTT | 7410 |
rs2810493 | snp | C/T | 0.427119 | 0.176434 | intron-variant | VAV2 | GRCh38.p7 | 9:133902013 | AGACTCTGTGGATGC[C/T]CCGAGCCTCCATGTC | 7410 |
rs2810496 | snp | A/G | 0.434543 | 0.168653 | intron-variant | VAV2 | GRCh38.p7 | 9:133903453 | CCACATCAGGCTCAA[A/G]AGACAGGGGCTGAAA | 7410 |
rs2810497 | snp | C/T | 0.321053 | 0.23969 | intron-variant | VAV2 | GRCh38.p7 | 9:133903686 | AGGTCTACCCCTGCT[C/T]CTAGGGCTCTGATCT | 7410 |
rs2810498 | snp | C/T | 0.499844 | 0.0463739 | intron-variant | VAV2 | GRCh38.p7 | 9:133903730 | GTCACTGAAAAACAG[C/T]GTCAGAAAAAATTCT | 7410 |
rs2810499 | snp | G/T | 0.254385 | 0.249962 | intron-variant | VAV2 | GRCh38.p7 | 9:133905085 | TGAGCAGCTGCCCTG[G/T]GCAAAGTCACTCACC | 7410 |
rs2810500 | snp | C/T | 0.21875 | 0.248039 | intron-variant | VAV2 | GRCh38.p7 | 9:133906267 | TGCCCAAGACAGTGA[C/T]GGAAACGCAGGGCTG | 7410 |
rs2810501 | snp | A/G | 0.209084 | 0.246629 | intron-variant | VAV2 | GRCh38.p7 | 9:133907565 | GCTCCACCACGTTGG[A/G]AAGCCCCCTGGGAGA | 7410 |
rs2810503 | snp | A/G | 0.253264 | 0.249979 | intron-variant | VAV2 | GRCh38.p7 | 9:133912683 | CCCAAGCTGTCAGGC[A/G]GCCATCCTCAGGGGC | 7410 |
rs2810504 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | VAV2 | GRCh38.p7 | 9:133913257 | GGCGCCACGGCCCCC[A/G]TGAGAAGGACGATAA | 7410 |
rs2810505 | snp | A/G | 0.426047 | 0.177503 | intron-variant | VAV2 | GRCh38.p7 | 9:133914441 | ATTCTTCAGCCAGAA[A/G]AAGGAACGAAGCGCT | 7410 |
rs2810506 | snp | A/G | 0.196264 | 0.252035 | intron-variant | VAV2 | GRCh38.p7 | 9:133915074 | GGAGTGCTTTGAAAC[A/G]GGCCGCTTGGCCGGA | 7410 |
rs2810507 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV2 | GRCh38.p7 | 9:133915186 | GTCCTCATTGGCTCT[A/G]GGGACATCAGGGAAT | 7410 |
rs2810508 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | VAV2 | GRCh38.p7 | 9:133920750 | ACAGCAGGCCAGTGC[C/T]GGGCAACATACTGGC | 7410 |
rs2810510 | snp | C/T | 0.268452 | 0.249318 | intron-variant | VAV2 | GRCh38.p7 | 9:133925989 | AAACTTAATTAACTG[C/T]GGACATGGACCAAAA | 7410 |
rs2810511 | snp | C/G | 0.252983 | 0.249982 | intron-variant | VAV2 | GRCh38.p7 | 9:133926419 | TATTATTACTAATTC[C/G]AACAACCTGGCTTGC | 7410 |
rs2810512 | snp | A/C | 0.254105 | 0.249966 | intron-variant | VAV2 | GRCh38.p7 | 9:133929503 | ACAGCACATGCCAGG[A/C]GGTTCCACGGGGGTA | 7410 |
rs2810513 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | VAV2 | GRCh38.p7 | 9:133930098 | TGACGCCGTCAGCAC[A/C]GACACCGGTGGTCAT | 7410 |
rs2810514 | snp | C/T | 0.254944 | 0.249951 | intron-variant | VAV2 | GRCh38.p7 | 9:133930236 | CTCCTCTCTGCCTCC[C/T]GGCATCCTCACTGCC | 7410 |
rs2810515 | snp | C/T | 0.254385 | 0.249962 | intron-variant | VAV2 | GRCh38.p7 | 9:133930497 | TCCCGGCATCCTGGC[C/T]GTCTTCCGTGCGCCT | 7410 |
rs2810516 | snp | A/G | 0.281841 | 0.247964 | intron-variant | VAV2 | GRCh38.p7 | 9:133930824 | TGGTGTGCGTCCAGC[A/G]TCGCCAGCTGGCACT | 7410 |
rs2810518 | snp | C/T | 0.338296 | 0.233889 | intron-variant | VAV2 | GRCh38.p7 | 9:133934060 | tggacagatgaatga[C/T]tgatggatagatgga | 7410 |
rs2810519 | snp | C/T | 0.337841 | 0.23406 | intron-variant | VAV2 | GRCh38.p7 | 9:133934114 | tggatggatgatgga[C/T]agatggatggatgga | 7410 |
rs2810520 | snp | G/T | 0.267364 | 0.249396 | intron-variant | VAV2 | GRCh38.p7 | 9:133935860 | TCCATTGCTCCCAAG[G/T]GTGCCAGCACCCAGC | 7410 |
rs2810521 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | VAV2 | GRCh38.p7 | 9:133935959 | CTCCAGGAGGCAAAG[A/G]GCATGGCTCAGATGC | 7410 |
rs2810522 | snp | A/G | 0.499035 | 0.0219437 | intron-variant | VAV2 | GRCh38.p7 | 9:133936682 | TCACAAACACCTCCT[A/G]TGGACCTCATCCAGT | 7410 |
rs2810523 | snp | A/G | 0.466204 | 0.125522 | intron-variant | VAV2 | GRCh38.p7 | 9:133937473 | AGTGTGAGTGTGAAC[A/G]TGTGTGGGGTGGGTG | 7410 |
rs2810524 | snp | A/G | 0.228253 | 0.249052 | intron-variant | VAV2 | GRCh38.p7 | 9:133938333 | CAGGAAGCTATTGAG[A/G]CCCTGATCCCATCCA | 7410 |
rs2810526 | snp | A/G | 0.228253 | 0.249052 | intron-variant | VAV2 | GRCh38.p7 | 9:133938714 | AGCCCCTTAGGAGGT[A/G]GTACTAACTTCGACC | 7410 |
rs2810527 | snp | A/G | 0.228253 | 0.249052 | intron-variant | VAV2 | GRCh38.p7 | 9:133938717 | CCCTTAGGAGGTGGT[A/G]CTAACTTCGACCCAT | 7410 |
rs2810528 | snp | A/G | 0.216048 | 0.247684 | intron-variant | VAV2 | GRCh38.p7 | 9:133938779 | AGGTAAATGCTCAGC[A/G]TCCCCTGGCTAGAAC | 7410 |
rs2810529 | snp | G/T | 0.16028 | 0.233346 | intron-variant | VAV2 | GRCh38.p7 | 9:133889735 | TCGGCTGTTTGTTCA[G/T]AAGACATTTCATTTA | 7410 |
rs2810530 | snp | A/G | 0.375797 | 0.216044 | intron-variant | VAV2 | GRCh38.p7 | 9:133939810 | CAGGGGCCACCCCCA[A/G]GAAGCCACGGAGGAC | 7410 |
rs2810531 | snp | A/G | 0.395635 | 0.2032 | intron-variant | VAV2 | GRCh38.p7 | 9:133940321 | GAGCCCAGGATTGTC[A/G]TCCTCATCAATAACC | 7410 |
rs2810532 | snp | C/G | 0.404384 | 0.196635 | intron-variant | VAV2 | GRCh38.p7 | 9:133940436 | CTTAGACATAGTGCA[C/G]GTCAGAATCAGAGCC | 7410 |
rs2810533 | snp | C/G | 0.425586 | 0.17796 | intron-variant | VAV2 | GRCh38.p7 | 9:133940447 | TGCACGTCAGAATCA[C/G]AGCCTAAGAGCGTAA | 7410 |
rs2810534 | snp | A/G | 0.372995 | 0.217652 | intron-variant | VAV2 | GRCh38.p7 | 9:133941103 | acacctgtgcccacc[A/G]aacactcaaatgtgg | 7410 |
rs2810536 | snp | G/T | 0.420255 | 0.183066 | intron-variant | VAV2 | GRCh38.p7 | 9:133947503 | TCAGGAGTTTGAGAC[G/T]ATCCTGACCAACATG | 7410 |
rs2810537 | snp | C/T | 0.426201 | 0.177351 | intron-variant | VAV2 | GRCh38.p7 | 9:133951817 | tgaggcttcaggaag[C/T]gtagttatctgcTTG | 7410 |
rs2810539 | snp | C/T | 0.478768 | 0.100824 | intron-variant | VAV2 | GRCh38.p7 | 9:133966102 | aaatgaaactagact[C/T]ccatgtctccccata | 7410 |
rs2810540 | snp | C/T | 0.450734 | 0.149016 | intron-variant | VAV2 | GRCh38.p7 | 9:133966523 | ctggcctgtgcaata[C/T]ggcgagaccccgtct | 7410 |
rs2810541 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | VAV2 | GRCh38.p7 | 9:133967930 | AGAGGAAGACTCTAT[A/C]ACCAAAAAAAAAAAA | 7410 |
rs2810542 | snp | C/G | 0.423726 | 0.179776 | intron-variant | VAV2 | GRCh38.p7 | 9:133970538 | GGCACCCACAGCCCT[C/G]TGGTTGGTGTACCTG | 7410 |
rs2810543 | snp | A/G | 0.157642 | 0.232314 | intron-variant | VAV2 | GRCh38.p7 | 9:133971141 | CCATCGCTTCCCCCA[A/G]CGAAGTCAGGCAGAG | 7410 |
rs2810544 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | VAV2 | GRCh38.p7 | 9:133972996 | GGGAGGCGGAGGAGG[A/C]GGGCACTGGGGAAGC | 7410 |
rs2810545 | snp | A/C | 0.135143 | 0.222054 | intron-variant | VAV2 | GRCh38.p7 | 9:133893924 | CACGGATCCTCACAG[A/C]CCTCTGGAAAGTTCT | 7410 |
rs2873805 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | VAV2 | GRCh38.p7 | 9:133776356 | TGGGACAGCAAGGAC[C/T]GAAGGTGCGGGAAGT | 7410 |
rs2873890 | snp | C/T | 0.342358 | 0.232314 | intron-variant | VAV2 | GRCh38.p7 | 9:133896921 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 7410 |
rs2905165 | snp | A/T | 0.306679 | 0.24349 | intron-variant | VAV2 | GRCh38.p7 | 9:133900029 | CCATCTCAAAAAAAA[A/T]AAATAAATAAATAAA | 7410 |
rs2993799 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | VAV2 | GRCh38.p7 | 9:133837301 | TGCCTTCTGATGCCT[C/G]GTTAGGGCCTAAGAG | 7410 |
rs2993800 | snp | A/T | 0.171704 | 0.237423 | intron-variant | VAV2 | GRCh38.p7 | 9:133837713 | CAAAAAAAATAAATT[A/T]AAAAAAAAAAAAAAA | 7410 |
rs2993801 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | VAV2 | GRCh38.p7 | 9:133839604 | acaggcgcccacccc[C/G]acgtccagctaattt | 7410 |
rs2995646 | snp | C/T | 0.458315 | 0.13822 | intron-variant | VAV2 | GRCh38.p7 | 9:133827251 | AGGTGGTGATGCCCC[C/T]GCTCAGTGGTCAGCC | 7410 |
rs2998895 | snp | G/T | 0.400147 | 0.19989 | intron-variant | VAV2 | GRCh38.p7 | 9:133958393 | CAGCAATACTGCTTT[G/T]TAAAGCATTGAGATG | 7410 |
rs3003582 | snp | A/G | 0.444444 | 0.157135 | intron-variant | VAV2 | GRCh38.p7 | 9:133827260 | CTGAGCGGGGGCATC[A/G]CCACCTACCGCTGCG | 7410 |
rs3003583 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133827274 | CGCCAGCTACTGCTG[C/T]GCCCACTGAGGCTGA | 7410 |
rs3003584 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | VAV2 | GRCh38.p7 | 9:133839570 | attcccctgtctcag[C/T]ctccaagtagctggg | 7410 |
rs3003585 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | VAV2 | GRCh38.p7 | 9:133839707 | gcccgcctcagcctc[C/T]caaagtgctgggatt | 7410 |
rs3003586 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133851888 | ataaatggatggatg[C/G]atggatggatggatg | 7410 |
rs3017466 | snp | G/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133818761 | gggtcatctgagggt[G/T]ggcttctattgactc | 7410 |
rs3017467 | snp | G/T | 0.203882 | 0.245709 | intron-variant | VAV2 | GRCh38.p7 | 9:133838116 | TTCACCAGGCCCCAG[G/T]CCCCTTTCACTCCGC | 7410 |
rs3017468 | snp | C/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133827466 | CACCACCTACCGCTG[C/T]GCCCACTGAGGCTGA | 7410 |
rs3017469 | snp | A/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133827715 | CCGCTGCGCCCACTG[A/G]GGCTGACCACTGAGC | 7410 |
rs3054960 | in-del | -/AC/CA/GC | | | intron-variant | VAV2 | GRCh38.p7 | 9:133854256 | CATGCACTCATCTGC[-/AC/CA/GC]ACACACACACGCACA | 7410 |
rs3054961 | in-del | -/AACA | | | intron-variant | VAV2 | GRCh38.p7 | 9:133854289 | CCATATGCACACACA[-/AACA]CACACCCATGTGCAC | 7410 |
rs3081203 | in-del | -/CCTGTG | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133786013 | GCACAGGTGCCTGTG[-/CCTGTG]TGAACACATGTTCTC | 7410 |
rs3780736 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV2 | GRCh38.p7 | 9:133820925 | AGAACTCAGCGAAGA[C/T]GCGGCACACGGAACC | 7410 |
rs3780737 | snp | C/T | 0.333722 | 0.235565 | intron-variant | VAV2 | GRCh38.p7 | 9:133867645 | AGCAGCAGCCAATGG[C/T]TTTCAGTGCCCCGCA | 7410 |
rs3780738 | snp | A/G | 0.349671 | 0.229272 | intron-variant | VAV2 | GRCh38.p7 | 9:133868280 | AGCACAGCAGGCACC[A/G]CATCCCCATGAGGTG | 7410 |
rs3780739 | snp | A/G | 0.172351 | 0.237636 | intron-variant | VAV2 | GRCh38.p7 | 9:133874826 | TCCATCTCCCTCCCC[A/G]GCCCACAACTGCAGA | 7410 |
rs3780740 | snp | A/G | 0.162581 | 0.234218 | intron-variant | VAV2 | GRCh38.p7 | 9:133874869 | GAAGTGGGGCGTGGA[A/G]GCCTCATGGAGCCAG | 7410 |
rs3780741 | snp | A/G | 0.153 | 0.230415 | intron-variant | VAV2 | GRCh38.p7 | 9:133874964 | ACACACAGAGAAGAC[A/G]GGTCTAGAAATGGGT | 7410 |
rs3780742 | snp | A/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133886263 | GAGGGGCTGGGCCTC[A/G]TCTGATGCTTGCCTC | 7410 |
rs3780748 | snp | C/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133892535 | TCAGCAAAAATCAAT[C/G]TGCATCAATCCCTGG | 7410 |
rs3780750 | snp | C/G | 0.132409 | 0.220618 | intron-variant | VAV2 | GRCh38.p7 | 9:133897253 | AGCAGCAGCAAGAGA[C/G]TAAGTCCCCCTCCTT | 7410 |
rs3780751 | snp | A/G | 0.399253 | 0.200558 | intron-variant | VAV2 | GRCh38.p7 | 9:133897336 | GGTCAGGAGCCCAGC[A/G]CAGGGCACACCCAGG | 7410 |
rs3780752 | snp | C/T | 0.393619 | 0.204631 | intron-variant | VAV2 | GRCh38.p7 | 9:133897399 | GCCCTGCTCTGCCCC[C/T]CTGTAACCCACCATC | 7410 |
rs3780753 | snp | C/T | 0.497907 | 0.0322805 | intron-variant | VAV2 | GRCh38.p7 | 9:133904965 | GGCAGGGAGGGGATG[C/T]AGGGAGCGCTTGGGA | 7410 |
rs3780754 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | VAV2 | GRCh38.p7 | 9:133905027 | CTTGGGCAGTGCCAC[A/G]GGCAGCACCACACGT | 7410 |
rs3780760 | snp | A/G | 0.287085 | 0.247234 | intron-variant | VAV2 | GRCh38.p7 | 9:133922047 | CATGCATGCAGGCAC[A/G]GGATGGGCCCCGCCT | 7410 |
rs3780761 | snp | C/T | 0.286564 | 0.247312 | intron-variant | VAV2 | GRCh38.p7 | 9:133922131 | TTGTTTGCCAGGTGG[C/T]AGCGGGAAGCTTCTC | 7410 |
rs3780762 | snp | C/T | 0.286564 | 0.247312 | intron-variant | VAV2 | GRCh38.p7 | 9:133922134 | TTTGCCAGGTGGCAG[C/T]GGGAAGCTTCTCCAG | 7410 |
rs3780763 | snp | G/T | 0.286564 | 0.247312 | intron-variant | VAV2 | GRCh38.p7 | 9:133922136 | TGCCAGGTGGCAGCG[G/T]GAAGCTTCTCCAGCC | 7410 |
rs3780764 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV2 | GRCh38.p7 | 9:133935048 | CCCACCCACCCCAGA[C/T]GACAGTCAGTTCTGA | 7410 |
rs3780768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV2 | GRCh38.p7 | 9:133942505 | CCGGGGCAGGGGCTA[C/T]GCCCTCTCGCTCATC | 7410 |
rs3780772 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | VAV2 | GRCh38.p7 | 9:133942578 | TTTTTTGAATATGGC[A/T]TGTCTGTAATTTCCA | 7410 |
rs3780775 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | VAV2 | GRCh38.p7 | 9:133944335 | GAGCTGGCATCTAGC[C/T]GGCATGACCTGAGAG | 7410 |
rs3780776 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV2 | GRCh38.p7 | 9:133944728 | CCTGTCTCGCCAAGG[A/C]CGGCAGCACAAGGCC | 7410 |
rs3780783 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | VAV2 | GRCh38.p7 | 9:133948246 | GTCTGGACAATTGAA[A/C]TTCCTTCGCTCGGGC | 7410 |
rs3780786 | snp | C/G | 0.155656 | 0.231515 | intron-variant | VAV2 | GRCh38.p7 | 9:133950943 | GACCCAAGCAGAGGG[C/G]GCGATTCTTCCCGTT | 7410 |
rs3780792 | snp | A/G | 0.388964 | 0.20782 | intron-variant | VAV2 | GRCh38.p7 | 9:133970221 | AAGTGCCAGGTCCTC[A/G]GCTCCCTGGGCACAG | 7410 |
rs3780794 | snp | C/G | 0.280256 | 0.248162 | intron-variant | VAV2 | GRCh38.p7 | 9:133972560 | CTCCTGCAAGCCTGA[C/G]CCCCCCTGAGAAACA | 7410 |
rs3780799 | snp | C/T | 0.267636 | 0.249377 | intron-variant | VAV2 | GRCh38.p7 | 9:133987681 | TGGGCAAGTCAGAGG[C/T]TGGGCGGCGGGTGGT | 7410 |
rs3819500 | snp | C/T | 0.185155 | 0.241444 | intron-variant | VAV2 | GRCh38.p7 | 9:133855677 | GACCAAAAGGTGGGT[C/T]CTTGAAGCCATAAGG | 7410 |
rs3819502 | snp | A/C | 0.433382 | 0.169915 | intron-variant | VAV2 | GRCh38.p7 | 9:133855956 | TGGCCTAGCCACACA[A/C]TGGAATGTTCCACGG | 7410 |
rs3819503 | snp | A/C | 0.416382 | 0.186593 | intron-variant | VAV2 | GRCh38.p7 | 9:133856305 | GTATTTCAATTTTTA[A/C]AAGTCAGAAAGCAGA | 7410 |
rs3819504 | snp | C/T | 0.253824 | 0.249971 | intron-variant | VAV2 | GRCh38.p7 | 9:133856441 | CCCCCCACCGGGACC[C/T]CATGCTGGTATGTGC | 7410 |
rs3819505 | snp | C/T | 0.253824 | 0.249971 | intron-variant | VAV2 | GRCh38.p7 | 9:133856471 | CCCCCCACCGGGACC[C/T]CATGCTGGTATGTGC | 7410 |
rs3824556 | snp | A/G | 0.454784 | 0.1434 | intron-variant | VAV2 | GRCh38.p7 | 9:133792530 | TGGGTGTGTGTTATT[A/G]TGTGTGTGTATGTGA | 7410 |
rs3824558 | snp | C/G | 0.491263 | 0.0655142 | intron-variant | VAV2 | GRCh38.p7 | 9:133792632 | TGTGTGTGTGAGCGT[C/G]TGTGTGCATGCACGC | 7410 |
rs3824559 | snp | A/G | 0.499885 | 0.00758699 | intron-variant | VAV2 | GRCh38.p7 | 9:133792652 | TGCATGCACGCACAT[A/G]CATGCAGGAGCTCAG | 7410 |
rs3824560 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | VAV2 | GRCh38.p7 | 9:133792747 | CTTCCTCCATCCTGC[C/T]GGGGAGGCCGCCCTC | 7410 |
rs3824561 | snp | C/T | 0.5 | 0.00019968 | intron-variant | VAV2 | GRCh38.p7 | 9:133792838 | AGGGAACACACTGAC[C/T]GAGAGCCACACCTCG | 7410 |
rs3837288 | in-del | -/A | 0.106987 | 0.205054 | intron-variant | VAV2 | GRCh38.p7 | 9:133864571 | CCACACAGCCACAGC[-/A]CAACCTTTTAAAGGC | 7410 |
rs3837289 | in-del | -/G | 0.188316 | 0.242271 | intron-variant | VAV2 | GRCh38.p7 | 9:133880143 | CCGTCTGCAGGAAGA[-/G]GGGCTAGGCATCCCT | 7410 |
rs3837291 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | VAV2 | GRCh38.p7 | 9:133905064 | TCTCCCAGGGCGGGG[-/A]GGCTCTGAGCAGCTG | 7410 |
rs3837293 | in-del | -/CCAGGC | | | intron-variant | VAV2 | GRCh38.p7 | 9:133959060 | CCCAGGGGCCCAGGC[-/CCAGGC]AGGGCTTGCAGCAGA | 7410 |
rs3842226 | in-del | -/A | 0.497359 | 0.0362457 | intron-variant | VAV2 | GRCh38.p7 | 9:133792673 | AGGAGCTCAGCCCCC[-/A]AAGGGACCCCCCCCC | 7410 |
rs3858098 | snp | C/T | 0.097727 | 0.198275 | intron-variant | VAV2 | GRCh38.p7 | 9:133772475 | agacaggcttgcgct[C/T]ggcacctctgaggag | 7410 |
rs3858099 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | VAV2 | GRCh38.p7 | 9:133819830 | GGAACTGAAATTTCA[C/T]GACACACATATTCTA | 7410 |
rs3858100 | snp | C/T | 0.312837 | 0.241974 | intron-variant | VAV2 | GRCh38.p7 | 9:133821050 | TCCTTGAAAAGCACC[C/T]CAAGGCCCTGCCACG | 7410 |
rs3858101 | snp | C/T | 0.311859 | 0.242226 | intron-variant | VAV2 | GRCh38.p7 | 9:133821120 | CACTCTCCTGTGGCT[C/T]TGTGGCAGGCTGCTG | 7410 |
rs3858102 | snp | C/T | 0.320335 | 0.239902 | intron-variant | VAV2 | GRCh38.p7 | 9:133821183 | TCGGCTAGAAAGAAG[C/T]GTGTGGAGGCTCCGT | 7410 |
rs3858103 | snp | A/T | 0.312348 | 0.242101 | intron-variant | VAV2 | GRCh38.p7 | 9:133821267 | TCTGGTCCACAGAGC[A/T]GGCCAGTCCTCATCA | 7410 |
rs3858104 | snp | A/G | 0.190205 | 0.242744 | intron-variant | VAV2 | GRCh38.p7 | 9:133883629 | GGCAGGTTTCAGCTC[A/G]GCCGGAGCAGGCCCT | 7410 |
rs3893493 | snp | A/G | 0.45866 | 0.137698 | intron-variant | VAV2 | GRCh38.p7 | 9:133828784 | ACTTGCGCTGGAACA[A/G]CCCTCAGCCACACCT | 7410 |
rs3902657 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | VAV2 | GRCh38.p7 | 9:133829590 | TGTGACACTGATCAC[A/C]AGGTGACCCAGATAA | 7410 |
rs3967928 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953124 | ACATCTAGAACCTCC[A/G]GAGGCAGCACAGCCC | 7410 |
rs3967929 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953154 | CTGCCAACACCTAGA[A/G]CTTCCAGAGGGAGCA | 7410 |
rs4058714 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953104 | GGAGGGAGCACAGCC[C/T]GCCAACATCTAGAAC | 7410 |
rs4058715 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953105 | GAGGGAGCACAGCCT[C/G]CCAACATCTAGAACC | 7410 |
rs4058716 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953106 | AGGGAGCACAGCCTG[A/C]CAACATCTAGAACCT | 7410 |
rs4058717 | snp | A/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953108 | GGAGCACAGCCTGCC[A/T]ACATCTAGAACCTCC | 7410 |
rs4058718 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953112 | CACAGCCTGCCAACA[C/T]CTAGAACCTCCAGAG | 7410 |
rs4058719 | in-del | -/CC | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953122 | ANACATCTAGAACCT[-/CC]AGAGGCAGCACAGCC | 7410 |
rs4058720 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953129 | TAGAACCTCCAGAGG[C/G]AGCACAGCCCTGCCA | 7410 |
rs4058721 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953165 | TAGAGCTTCCAGAGG[C/G]AGCACAGCCCTGCTG | 7410 |
rs4058722 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV2 | GRCh38.p7 | 9:133953179 | GGAGCACAGCCCTGC[A/C/T]GACACCTTGGTTTCA | 7410 |
rs4058723 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953180 | GAGCACAGCCCTGCT[A/G]ACACCTTGGTTTCAG | 7410 |
rs4058724 | in-del | -/ACAAAAAT | | | intron-variant | VAV2 | GRCh38.p7 | 9:133976051 | aaaaaaanngaaaat[-/ACAAAAAT]nnnnnnntagccagg | 7410 |
rs4058727 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953031 | AACCTGGAGGGAGCA[C/T]GGCCCCACTGACACC | 7410 |
rs4058728 | snp | G/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953040 | GGAGCACGGCCCCAC[G/T]GACACCTAGAACCTG | 7410 |
rs4058729 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133953100 | ACCTGGAGGGAGCAC[A/G]GCCTGCCAACATCTA | 7410 |
rs4059239 | snp | C/T | 0.325327 | 0.238382 | intron-variant | VAV2 | GRCh38.p7 | 9:133821213 | TGTCATCAGAGGCTA[C/T]ACTTCGTGGAAAAAC | 7410 |
rs4078571 | snp | C/G | 0.016162 | 0.0884297 | intron-variant | VAV2 | GRCh38.p7 | 9:133834361 | GAAGAGAAGGCGAGA[C/G]GGAGGTGAGCAGGTC | 7410 |
rs4081338 | snp | C/G | 0.21875 | 0.248039 | intron-variant | VAV2 | GRCh38.p7 | 9:133828449 | CTGGCGATGCCCGTG[C/G]TCAGTGGTCAGCCCC | 7410 |
rs4285539 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | VAV2 | GRCh38.p7 | 9:133946724 | ATCAATAAAAAAATG[A/G]GAAAACAAATTAATT | 7410 |
rs4308797 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | VAV2 | GRCh38.p7 | 9:133922733 | acctaaacataagag[C/T]taaaactataaaact | 7410 |
rs4406471 | snp | C/T | 0.392881 | 0.205147 | intron-variant | VAV2 | GRCh38.p7 | 9:133897110 | AAAAAAAATCCCAAC[C/T]GAAACAGATGTTGGG | 7410 |
rs4436183 | snp | C/T | 0.346811 | 0.230494 | intron-variant | VAV2 | GRCh38.p7 | 9:133897010 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 7410 |
rs4744524 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV2 | GRCh38.p7 | 9:133875800 | cctgcctgggctaag[A/G]ggtacccagagggca | 7410 |
rs4744525 | snp | A/C | 0.112631 | 0.208878 | intron-variant | VAV2 | GRCh38.p7 | 9:133904602 | AGGCATGCAGGCATG[A/C]AGCACACCCTCTCCC | 7410 |
rs4744527 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | VAV2 | GRCh38.p7 | 9:133947654 | CAGTGAGCCGAGATC[A/G]TGCCATTGCACTCCA | 7410 |
rs4744536 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | VAV2 | GRCh38.p7 | 9:133913394 | CCTCACTACACCAGC[A/G]AGAAGAAGAAACCAA | 7410 |
rs4744537 | snp | A/G | 0.428937 | 0.17459 | intron-variant | VAV2 | GRCh38.p7 | 9:133957972 | attaagggcggtgca[A/G]gatgtgctttgttaa | 7410 |
rs4744538 | snp | C/G | 0.5 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133958013 | gaaggcagcatgctc[C/G]ttaagagtcatcacc | 7410 |
rs4744539 | snp | C/T | 0.499879 | 0.0077866 | intron-variant | VAV2 | GRCh38.p7 | 9:133964050 | ATATATATATATATA[C/T]ATATATATACATATA | 7410 |
rs4744540 | snp | C/T | 0.470618 | 0.117591 | intron-variant | VAV2 | GRCh38.p7 | 9:133964060 | ATATACATATATATA[C/T]ATATATATAAATGAA | 7410 |
rs4744541 | snp | A/G | 0.45692 | 0.1403 | intron-variant | VAV2 | GRCh38.p7 | 9:133966475 | ctttgagaggccgag[A/G]cgggaagatggcttg | 7410 |
rs4744542 | snp | A/T | 0.428182 | 0.17536 | intron-variant | VAV2 | GRCh38.p7 | 9:133966725 | AAAAATTTAAAACTT[A/T]AAAAAAAAAAAGTCA | 7410 |
rs5901027 | in-del | -/CAGACA | 0.413914 | 0.188765 | intron-variant | VAV2 | GRCh38.p7 | 9:133772635 | CACCCACCCCCTTGC[-/CAGACA]CAGACATCACAAGAA | 7410 |
rs5901028 | in-del | -/G | 0.0275645 | 0.114116 | intron-variant | VAV2 | GRCh38.p7 | 9:133897642 | TCTGGGTGGCCAAAA[-/G]GTGTGGCTCTAAGCC | 7410 |
rs5901029 | in-del | -/AAAA | | | intron-variant | VAV2 | GRCh38.p7 | 9:133905450 | AAAAAAAAAAAAAAA[-/AAAA]GAAACAAAAGAAGAA | 7410 |
rs6479622 | snp | C/T | 0.208474 | 0.246527 | intron-variant | VAV2 | GRCh38.p7 | 9:133772985 | CACAACTAGGCTGGA[C/T]GGCAGAGCCTACTGC | 7410 |
rs6479623 | snp | A/G | 0.496034 | 0.0443518 | intron-variant | VAV2 | GRCh38.p7 | 9:133793238 | CACAGCGGAACCCAA[A/G]GGAGCCGGCCACGTG | 7410 |
rs6479624 | snp | C/T | 0.302435 | 0.244439 | intron-variant | VAV2 | GRCh38.p7 | 9:133820348 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTGTCG | 7410 |
rs6479625 | snp | C/T | 0.301932 | 0.244547 | intron-variant | VAV2 | GRCh38.p7 | 9:133820392 | GCAGTGGCACTATCT[C/T]GGCTCACTGCAGGCT | 7410 |
rs6479627 | snp | C/T | 0.474182 | 0.110646 | intron-variant | VAV2 | GRCh38.p7 | 9:133868335 | AAATGAGTCTTCTGG[C/T]TCTGGCCAGGAGATG | 7410 |
rs7018464 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133832880 | TTGAAGTCTCCCTCA[A/G]ATTCCTGAGGCTGGT | 7410 |
rs7018604 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | VAV2 | GRCh38.p7 | 9:133832951 | GCTGTGACCTGCATG[A/G]CCCCTGTGCCCATCT | 7410 |
rs7018770 | snp | A/G | 0.269267 | 0.249256 | intron-variant | VAV2 | GRCh38.p7 | 9:133983699 | CCCCGGGTCCTTCCT[A/G]CTGACCCCAGGCCTG | 7410 |
rs7019167 | snp | A/C | 0.493432 | 0.0569306 | intron-variant | VAV2 | GRCh38.p7 | 9:133794996 | GTGCACCTGAGCCAA[A/C]ACCCGGAGCCGGGGA | 7410 |
rs7020602 | snp | A/G | 0.000312945 | 0.012505 | synonymous-codon | VAV2 | GRCh38.p7 | 9:133939196 | GACTTTCAGGAAGGT[A/G]CGTATGTTCTTCAAA | 7410 |
rs7020737 | snp | C/T | 0.270351 | 0.24917 | intron-variant | VAV2 | GRCh38.p7 | 9:133817423 | tttgggaggccgagg[C/T]gggtggatcacctga | 7410 |
rs7020756 | snp | A/C/G | 0.00795532 | 0.062565 | intron-variant | VAV2 | GRCh38.p7 | 9:133909275 | GGTGAAGATGTGAGC[A/C/G]GCCTCCCCCAAGTCC | 7410 |
rs7021311 | snp | C/T | 0.365439 | 0.221752 | intron-variant | VAV2 | GRCh38.p7 | 9:133989206 | agctgggcatggtgg[C/T]gcatgcctgtcatcc | 7410 |
rs7021663 | snp | C/T | 0.385932 | 0.209815 | intron-variant | VAV2 | GRCh38.p7 | 9:133810892 | CTGCTGAAGTTTACC[C/T]GCAGGACGCCCAGCT | 7410 |
rs7021946 | snp | A/T | 0.384401 | 0.210799 | intron-variant | VAV2 | GRCh38.p7 | 9:133811153 | GGGAGACCCCCCGGT[A/T]ATGGCGGGGAACAAA | 7410 |
rs7021948 | snp | A/C | 0.322721 | 0.23919 | intron-variant | VAV2 | GRCh38.p7 | 9:133871951 | TGGCTCCATGGGGTC[A/C]TCGCTCCACCCTTCC | 7410 |
rs7022082 | snp | A/T | 0.27008 | 0.249192 | intron-variant | VAV2 | GRCh38.p7 | 9:133872065 | CAGGCACTGGCACAG[A/T]GGGCAGACCTGAAAA | 7410 |
rs7022675 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | VAV2 | GRCh38.p7 | 9:133951737 | GCTTTTAGGCTGCTC[A/G]GCTCTGCTGCAGGAA | 7410 |
rs7022973 | snp | A/G | 0.176861 | 0.239062 | intron-variant | VAV2 | GRCh38.p7 | 9:133866763 | gtgggccgagattgc[A/G]ccactgcactccaac | 7410 |
rs7023452 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV2 | GRCh38.p7 | 9:133976474 | CCTAGTAAGAAGATG[A/G]GCTCTGCCTCGGGGT | 7410 |
rs7023551 | snp | A/G | 0.422158 | 0.181278 | intron-variant | VAV2 | GRCh38.p7 | 9:133859892 | TGGGGCCTCAGAGGC[A/G]TTAGTTATCCTCTAG | 7410 |
rs7024367 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV2 | GRCh38.p7 | 9:133977093 | CCAGCTCCAGGCCCA[A/G]GCCACGCCCAGCCGC | 7410 |
rs7025087 | snp | A/G | 0.493432 | 0.0569306 | intron-variant | VAV2 | GRCh38.p7 | 9:133794890 | CAGTTCCCTGAGGAC[A/G]GAACCCAGTGGGGGG | 7410 |
rs7025684 | snp | C/T | 0.27008 | 0.249192 | intron-variant | VAV2 | GRCh38.p7 | 9:133871783 | TCGACCAAGGTCTCA[C/T]TGCTGTGGGAGGCTG | 7410 |
rs7025729 | snp | C/T | 0.27008 | 0.249192 | intron-variant | VAV2 | GRCh38.p7 | 9:133871881 | GGTGGGGGCCAGCCC[C/T]GCCCCTTCTGAGCCC | 7410 |
rs7025939 | snp | C/T | 0.270892 | 0.249126 | intron-variant | VAV2 | GRCh38.p7 | 9:133871996 | CCACTGGGAATGAAA[C/T]GTTGGGATTCTAGTC | 7410 |
rs7025962 | snp | A/G | 0.084728 | 0.187577 | intron-variant | VAV2 | GRCh38.p7 | 9:133870031 | TTTTTCTTGTGGAAA[A/G]CACGGACAGAAAAAT | 7410 |
rs7025983 | snp | A/C | 0.227074 | 0.248947 | intron-variant | VAV2 | GRCh38.p7 | 9:133773909 | gtaggtttgtttaca[A/C]cagcataaccacact | 7410 |
rs7026235 | snp | A/G | 0.270621 | 0.249148 | intron-variant | VAV2 | GRCh38.p7 | 9:133870278 | TGCAGGAAGAGAGGT[A/G]GGAGCCGCCCCCAGG | 7410 |
rs7026263 | snp | A/G | 0.264906 | 0.249555 | intron-variant | VAV2 | GRCh38.p7 | 9:133817286 | atacccgtgttagac[A/G]tcctgacatcatccc | 7410 |
rs7026295 | snp | A/G | 0.265727 | 0.249505 | intron-variant | VAV2 | GRCh38.p7 | 9:133817360 | cctgttatttgaagt[A/G]tgtaacttccagcct | 7410 |
rs7026306 | snp | A/G | 0.265453 | 0.249522 | intron-variant | VAV2 | GRCh38.p7 | 9:133817379 | aacttccagcctggc[A/G]tggtggcgcacgcct | 7410 |
rs7026403 | snp | C/T | 0.265727 | 0.249505 | intron-variant | VAV2 | GRCh38.p7 | 9:133774272 | CACCATGAGTGTGTG[C/T]GCCCTACCCCCAGCT | 7410 |
rs7026404 | snp | A/C | 0.264084 | 0.249603 | intron-variant | VAV2 | GRCh38.p7 | 9:133774279 | AGTGTGTGCGCCCTA[A/C]CCCCAGCTCCTGGTC | 7410 |
rs7026413 | snp | A/C | 0.0887219 | 0.191022 | intron-variant | VAV2 | GRCh38.p7 | 9:133889761 | ATTTACACACACACA[A/C]AAAAAATTTTTTTCT | 7410 |
rs7026775 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | VAV2 | GRCh38.p7 | 9:133776839 | CTTCAGAGGTTCCAC[A/G]CTCTCACTCTGAGCT | 7410 |
rs7026854 | snp | C/T | 0.176861 | 0.239062 | intron-variant | VAV2 | GRCh38.p7 | 9:133866760 | ccagtgggccgagat[C/T]gcaccactgcactcc | 7410 |
rs7027267 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | VAV2 | GRCh38.p7 | 9:133859805 | AAAAACAATTAAACA[G/T]GTTTTAAACGGTGCC | 7410 |
rs7027503 | snp | C/T | 0.492237 | 0.0618148 | intron-variant | VAV2 | GRCh38.p7 | 9:133789529 | GAGGGTGCAGAAGAC[C/T]GGGAAGGGACTGGGC | 7410 |
rs7027518 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133989354 | caaaaaaaaaaaaaa[A/C]caaaaaatacaaaaa | 7410 |
rs7027703 | snp | A/G | 0.104859 | 0.203554 | intron-variant | VAV2 | GRCh38.p7 | 9:133925771 | CCTATCTACCTTCAA[A/G]AAACCAGTACTCCTG | 7410 |
rs7027853 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | VAV2 | GRCh38.p7 | 9:133893157 | TGAGTCCCACCTCCC[C/G]CGAAGACTCCTCTTG | 7410 |
rs7027965 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133975201 | AGGCACCCCAGCCTG[C/T]CCCGGCACCCCCGCC | 7410 |
rs7028095 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV2 | GRCh38.p7 | 9:133786439 | CTGCACTCCTGCCTG[C/T]GCCCATGTGCGAGGA | 7410 |
rs7028795 | snp | C/T | 0.031825 | 0.122064 | intron-variant | VAV2 | GRCh38.p7 | 9:133912699 | GCCATCCTCAGGGGC[C/T]GCAGTCACCGGTGGT | 7410 |
rs7029322 | snp | A/G | 0.353154 | 0.227726 | intron-variant | VAV2 | GRCh38.p7 | 9:133818659 | ggcctccataattgc[A/G]taagccaattcccat | 7410 |
rs7029488 | snp | A/G | 0.265453 | 0.249522 | intron-variant | VAV2 | GRCh38.p7 | 9:133817391 | ggcgtggtggcgcac[A/G]cctgtaatcccagca | 7410 |
rs7029750 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | VAV2 | GRCh38.p7 | 9:133817592 | cagcctgggagacaa[C/G]agtgaaactctgtct | 7410 |
rs7030082 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | VAV2 | GRCh38.p7 | 9:133832404 | GCTGGGGGTTGGGGC[C/T]TTATCCCTAAGGGAC | 7410 |
rs7030201 | snp | C/T | 0.253264 | 0.249979 | intron-variant | VAV2 | GRCh38.p7 | 9:133862624 | ACAAGAAAAGGCCCA[C/T]GACGGCCACGTGCCG | 7410 |
rs7031085 | snp | A/G | 0.084728 | 0.187577 | intron-variant | VAV2 | GRCh38.p7 | 9:133814026 | CACCCGCCCTCCACC[A/G]TGAGAGGTCCATCTG | 7410 |
rs7031569 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | VAV2 | GRCh38.p7 | 9:133986513 | gttggctggatggag[A/G]cggattgatgctgtt | 7410 |
rs7031854 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | VAV2 | GRCh38.p7 | 9:133798743 | GCCAGGTGCTCTGCC[A/G]ACAAGCCTTATGACT | 7410 |
rs7031860 | snp | A/C | 0.373598 | 0.21731 | intron-variant | VAV2 | GRCh38.p7 | 9:133986711 | AAATCTATCCCCCCC[A/C]AAAAAAGAAAAGACG | 7410 |
rs7032121 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV2 | GRCh38.p7 | 9:133820741 | GAGGGCCACAGCTGT[C/T]CACTGGGAGGAAGAG | 7410 |
rs7032354 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV2 | GRCh38.p7 | 9:133883412 | AGTCAGGGCCAGGGA[A/G]AGGAACAGAGCCGAG | 7410 |
rs7032358 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | VAV2 | GRCh38.p7 | 9:133883420 | CCAGGGAGAGGAACA[C/G]AGCCGAGTCAGCTGC | 7410 |
rs7032391 | snp | C/G | 0.499977 | 0.00339449 | intron-variant | VAV2 | GRCh38.p7 | 9:133790872 | CTGCCAGCTTCATGT[C/G]AGTGAAATCACCAGG | 7410 |
rs7032952 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | VAV2 | GRCh38.p7 | 9:133791272 | CCAGACTCTGGGGAG[C/T]CCCAGGAGGTGGCAG | 7410 |
rs7033494 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | VAV2 | GRCh38.p7 | 9:133879654 | GCCGCACACACCAGG[A/G]CGAACAGCACTGCTG | 7410 |
rs7033537 | snp | A/C | 0.322721 | 0.23919 | intron-variant | VAV2 | GRCh38.p7 | 9:133815800 | tgtatgcacgcacgc[A/C]tgtgtggtgggtggg | 7410 |
rs7033941 | snp | C/T | 0.039522 | 0.134904 | intron-variant | VAV2 | GRCh38.p7 | 9:133876322 | CACGCCCTGCTCCCA[C/T]GCCCAGCACCACTGA | 7410 |
rs7034116 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | VAV2 | GRCh38.p7 | 9:133841459 | CCCTGTTTCCCTGGG[A/G]ACAACCACCACCTCA | 7410 |
rs7034680 | snp | A/G | 0.351635 | 0.228408 | intron-variant | VAV2 | GRCh38.p7 | 9:133820373 | CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGCACTA | 7410 |
rs7034764 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | VAV2 | GRCh38.p7 | 9:133811818 | ATCCCATGGCAACAC[A/G]GGCGGGGGTCATGAC | 7410 |
rs7034805 | snp | A/G | 0.28171 | 0.253579 | intron-variant | VAV2 | GRCh38.p7 | 9:133872059 | GACTCTCAGGCACTG[A/G]CACAGAGGGCAGACC | 7410 |
rs7035398 | snp | A/G | 0.19646 | 0.2442 | intron-variant | VAV2 | GRCh38.p7 | 9:133771412 | TTCTGTGGCCATAGC[A/G]GGGAAGCTAAGAGCC | 7410 |
rs7035905 | snp | A/T | 0.243633 | 0.249919 | intron-variant | VAV2 | GRCh38.p7 | 9:133773847 | tgatcacatactatg[A/T]atgtgcagaattgtt | 7410 |
rs7036113 | snp | C/T | 0.243633 | 0.249919 | intron-variant | VAV2 | GRCh38.p7 | 9:133773989 | tcagctccattataa[C/T]cttacgggaccacca | 7410 |
rs7036180 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | VAV2 | GRCh38.p7 | 9:133939475 | AGGGTGTAGCCACCA[C/T]CGCCCCCAGCCTTCT | 7410 |
rs7036356 | snp | C/T | 0.079617 | 0.182947 | intron-variant | VAV2 | GRCh38.p7 | 9:133881841 | AGAGTTCAGTGGCCC[C/T]GGCTGGCATCACGGC | 7410 |
rs7036496 | snp | A/G | 0.209693 | 0.246729 | intron-variant | VAV2 | GRCh38.p7 | 9:133830010 | TAGGAACCAGCTGAC[A/G]ATGGAATGAACGATG | 7410 |
rs7037436 | snp | G/T | 0.49334 | 0.057322 | intron-variant | VAV2 | GRCh38.p7 | 9:133794705 | CGACGAGGGAGATGT[G/T]GGGGGGGTCGTCATC | 7410 |
rs7037437 | snp | A/G | 0.49334 | 0.057322 | intron-variant | VAV2 | GRCh38.p7 | 9:133794711 | GGGAGATGTGGGGGG[A/G]GTCGTCATCCCTCCA | 7410 |
rs7037626 | snp | C/T | 0.302435 | 0.244439 | intron-variant | VAV2 | GRCh38.p7 | 9:133819779 | GAACACTGGGAGAGA[C/T]GGGTTCCTCTGTGTC | 7410 |
rs7037681 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | VAV2 | GRCh38.p7 | 9:133973077 | TAAGGAATCCCCAGG[A/G]AGCCCTGCCTTGGTA | 7410 |
rs7038003 | snp | C/T | 0.344592 | 0.231414 | intron-variant | VAV2 | GRCh38.p7 | 9:133820020 | CCAGTATTTCTCCTA[C/T]GACCGATTCTGCATC | 7410 |
rs7038080 | snp | A/G | 0.49334 | 0.057322 | intron-variant | VAV2 | GRCh38.p7 | 9:133795205 | GAGCTGAGCTCACCC[A/G]GACAAGGGGAGAGAG | 7410 |
rs7038187 | snp | C/G | 0.493568 | 0.0563433 | intron-variant | VAV2 | GRCh38.p7 | 9:133795301 | TGAGAGATGGCACCG[C/G]AGGTGGCATTTTAGA | 7410 |
rs7038256 | snp | C/T | 0.270621 | 0.249148 | intron-variant | VAV2 | GRCh38.p7 | 9:133870098 | GAGTAGTGATAATTA[C/T]AAAACATGTGCAATC | 7410 |
rs7038489 | snp | C/T | 0.265453 | 0.249522 | intron-variant | VAV2 | GRCh38.p7 | 9:133817346 | aggcttctttcctcc[C/T]tgttatttgaagtgt | 7410 |
rs7039067 | snp | A/C | 0.499984 | 0.00279548 | intron-variant | VAV2 | GRCh38.p7 | 9:133791313 | TGGGGTCCGAGGAGC[A/C]GAGGCGACTGCCGGC | 7410 |
rs7039465 | snp | A/G | 0.232943 | 0.249417 | intron-variant | VAV2 | GRCh38.p7 | 9:133903597 | GACACAAAGTCGGAC[A/G]TGGCCTCAGCCAGCC | 7410 |
rs7040162 | snp | A/G | 0.316243 | 0.241064 | intron-variant | VAV2 | GRCh38.p7 | 9:133918383 | CCGGACCCAGGCCCA[A/G]CTGCTAGCCCGGGCT | 7410 |
rs7040634 | snp | A/G | 0.408359 | 0.193449 | intron-variant | VAV2 | GRCh38.p7 | 9:133800867 | GGCAAACTTCTACTC[A/G]TCTGTCAAAACTCTT | 7410 |
rs7040637 | snp | C/G | 0.309401 | 0.24284 | intron-variant | VAV2 | GRCh38.p7 | 9:133800871 | AACTTCTACTCGTCT[C/G]TCAAAACTCTTCCCT | 7410 |
rs7041512 | snp | A/G | 0.226188 | 0.248863 | intron-variant | VAV2 | GRCh38.p7 | 9:133889292 | AGGGTGGGGGCTCAC[A/G]GGCACGAGCCTAGAA | 7410 |
rs7042174 | snp | A/C | 0.288646 | 0.246995 | intron-variant | VAV2 | GRCh38.p7 | 9:133916533 | AAGCTGGGCAGTTTG[A/C]GGATGTGGGGCTGGG | 7410 |
rs7042276 | snp | C/T | 0.115438 | 0.210697 | intron-variant | VAV2 | GRCh38.p7 | 9:133810617 | ACAGCTCGAGACCAG[C/T]GGGACCAGCGCTGGG | 7410 |
rs7042486 | snp | C/G | 0.0376037 | 0.131863 | upstream-variant-2KB | VAV2 | GRCh38.p7 | 9:133993704 | GAGACTGGCTCAGCC[C/G]GGAGGCTGGGGTGCG | 7410 |
rs7042529 | snp | A/G | 0.353587 | 0.22753 | intron-variant | VAV2 | GRCh38.p7 | 9:133819102 | AACATTCCTTCACAC[A/G]GGCTCATTCTTCATG | 7410 |
rs7043422 | snp | A/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133869450 | atctctacaaaaaat[A/T]aaaaaaaaaaataac | 7410 |
rs7044093 | snp | A/G | 0.137867 | 0.223442 | intron-variant | VAV2 | GRCh38.p7 | 9:133902227 | ACGGGCATCTGCGTC[A/G]GACGTGTGAGGACCA | 7410 |
rs7044185 | snp | A/T | 0.394354 | 0.204112 | intron-variant | VAV2 | GRCh38.p7 | 9:133870037 | TTGTGGAAAGCACGG[A/T]CAGAAAAATTTGGGG | 7410 |
rs7044881 | snp | C/T | 0.117886 | 0.21224 | intron-variant | VAV2 | GRCh38.p7 | 9:133793496 | GTCGTTGTCCACTTG[C/T]CTTTAAAATAAGGAA | 7410 |
rs7045014 | snp | C/T | 0.120674 | 0.21395 | intron-variant | VAV2 | GRCh38.p7 | 9:133793612 | CCACCGCGGCCCCTG[C/T]GTGCACCTGGCCCAA | 7410 |
rs7046253 | snp | C/G | 0.302936 | 0.244331 | intron-variant | VAV2 | GRCh38.p7 | 9:133819725 | TGGCACTTTTCATTC[C/G]TCCAAAGCGCTCTCC | 7410 |
rs7046381 | snp | A/C | 0.27008 | 0.249192 | intron-variant | VAV2 | GRCh38.p7 | 9:133871692 | TAATGGTGGGGGGtc[A/C]caaccacccaccatg | 7410 |
rs7046387 | snp | C/G | 0.236724 | 0.249647 | intron-variant | VAV2 | GRCh38.p7 | 9:133789711 | AAGCCCCACGTTCAG[C/G]AGAGAACAAACAGCG | 7410 |
rs7046600 | snp | C/G | 0.119978 | 0.213528 | intron-variant | VAV2 | GRCh38.p7 | 9:133929627 | GCCCCTCTGCCTGCA[C/G]GCAAAAGCCAAGGGG | 7410 |
rs7047672 | snp | A/G | 0.115788 | 0.21092 | intron-variant | VAV2 | GRCh38.p7 | 9:133814799 | GGTTGCTGACGACAT[A/G]CAACGTCTTTCCTCT | 7410 |
rs7047679 | snp | C/G | 0.175897 | 0.238765 | intron-variant | VAV2 | GRCh38.p7 | 9:133866735 | ggcttgaacccagga[C/G]gtggaggttccagtg | 7410 |
rs7047927 | snp | C/T | 0.265453 | 0.249522 | intron-variant | VAV2 | GRCh38.p7 | 9:133816985 | TCCTCTGCATCTCCA[C/T]GTAAACTTTACAACC | 7410 |
rs7048218 | snp | C/G | 0.201727 | 0.245295 | intron-variant | VAV2 | GRCh38.p7 | 9:133867084 | GAGGACACGCCCCTG[C/G]AGGGGACACAACACC | 7410 |
rs7048247 | snp | C/T | 0.308661 | 0.24302 | intron-variant | VAV2 | GRCh38.p7 | 9:133817272 | gagagactgcaataa[C/T]acccgtgttagacgt | 7410 |
rs7048365 | snp | C/T | 0.265727 | 0.249505 | intron-variant | VAV2 | GRCh38.p7 | 9:133817327 | ggctctgtcccttct[C/T]tccaggcttctttcc | 7410 |
rs7048660 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | VAV2 | GRCh38.p7 | 9:133818167 | caggagatcgagacc[A/G]tcctgtctaacatga | 7410 |
rs7048686 | snp | G/T | 0.0770498 | 0.180522 | intron-variant | VAV2 | GRCh38.p7 | 9:133864549 | GACACCGGCAGCCCG[G/T]CAGCCTCCACACAGC | 7410 |
rs7048856 | snp | C/G | 0.286303 | 0.24735 | intron-variant | VAV2 | GRCh38.p7 | 9:133830185 | GGTCTGGGCAGTCAG[C/G]GGAGTCCTTTAGACA | 7410 |
rs7048989 | snp | A/G | 0.199873 | 0.244923 | intron-variant | VAV2 | GRCh38.p7 | 9:133936298 | CTCAGGCTAAAGTGC[A/G]GTGGCGTGATCTCTG | 7410 |
rs7388707 | snp | C/G | 0.41833 | 0.184838 | intron-variant | VAV2 | GRCh38.p7 | 9:133958363 | cgccttagggctgga[C/G]gtgggacctgcgggc | 7410 |
rs7389690 | snp | A/C | | | intron-variant | VAV2 | GRCh38.p7 | 9:133958231 | agtaaaagaggaagg[A/C]atgcctcttgcagtt | 7410 |
rs7390480 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133958233 | taaaagaggaaggca[C/T]gcctcttgcagttga | 7410 |
rs7390484 | snp | C/T | 0.5 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133958277 | catctgtctcctgcc[C/T]gtccctgggcaatgg | 7410 |
rs7847503 | snp | A/G | 0.142609 | 0.225759 | intron-variant | VAV2 | GRCh38.p7 | 9:133923940 | ggtgggaattgaaca[A/G]tgagaacacttggac | 7410 |
rs7847765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV2 | GRCh38.p7 | 9:133797587 | ACAAAAAACCATTAC[A/G]TCATCACCCCCATCA | 7410 |
rs7848329 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133900477 | aactgtccctccacc[C/G]tatctgtataaaaac | 7410 |
rs7848976 | snp | C/T | 0.155656 | 0.231515 | intron-variant | VAV2 | GRCh38.p7 | 9:133793303 | TGGAATTCCCCAAAA[C/T]GCAAGTGACCAGCCA | 7410 |
rs7849102 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV2 | GRCh38.p7 | 9:133845597 | AGGGTCAGCTGGGTG[A/G]CCGAGGCCTTGGCAG | 7410 |
rs7850025 | snp | A/C | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133895832 | ctactttaaaaaGAG[A/C]AAGAACATCAGCTTT | 7410 |
rs7850812 | snp | C/T | 0.295343 | 0.245854 | intron-variant | VAV2 | GRCh38.p7 | 9:133805705 | TCCACGTGCCACCTC[C/T]TTTCATCCTTGTCCA | 7410 |
rs7851037 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133900312 | TACTGGGGCTCAGAA[A/G]ACACTCCAACATGAA | 7410 |
rs7851059 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133900369 | cccctggagctggcc[A/G]tagaaactagaatgc | 7410 |
rs7851180 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | VAV2 | GRCh38.p7 | 9:133825846 | GGCAGCTCCCACTCA[C/T]TCCCCATGTAGAAAG | 7410 |
rs7852459 | snp | C/G | 0.235854 | 0.249599 | intron-variant | VAV2 | GRCh38.p7 | 9:133882117 | GGCAGGCCCCAGGCT[C/G]TACGGGACACAGTGG | 7410 |
rs7853193 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | VAV2 | GRCh38.p7 | 9:133876685 | CCGCGGGAGGGGGGC[A/G]GCCCCAAGGAGTCTT | 7410 |
rs7853626 | snp | C/G | 0.301932 | 0.244547 | intron-variant | VAV2 | GRCh38.p7 | 9:133861504 | ACAGAACTGGGGACG[C/G]TGCTTTGCAGGACGT | 7410 |
rs7854253 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133949874 | TGCCCCCGACCCGGG[C/T]GTCTCCTGCTGTTTA | 7410 |
rs7854365 | snp | A/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133900045 | aaataaataaataaa[A/T]aaaaatagctgggca | 7410 |
rs7854494 | snp | A/C/G | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133950019 | CGTGAAGTCCAGGAA[A/C/G]CCCAGTGCTGGGGCT | 7410 |
rs7855196 | snp | A/G | 0.23846 | 0.249734 | intron-variant | VAV2 | GRCh38.p7 | 9:133925428 | tcaccacgttgtcca[A/G]gctggtcttaaactc | 7410 |
rs7855827 | snp | C/T | 0.239326 | 0.249772 | intron-variant | VAV2 | GRCh38.p7 | 9:133925337 | ttcttctgcctcagc[C/T]tcccaagtagctggg | 7410 |
rs7855899 | snp | C/T | 0.407502 | 0.194147 | intron-variant | VAV2 | GRCh38.p7 | 9:133800186 | CCTGGCTGTGCCTCC[C/T]ATCTGATGATGACAC | 7410 |
rs7855970 | snp | A/G | 0.147991 | 0.228242 | intron-variant | VAV2 | GRCh38.p7 | 9:133868288 | AGGCACCGCATCCCC[A/G]TGAGGTGGGGCGCGG | 7410 |
rs7856275 | snp | A/G | 0.215747 | 0.247642 | intron-variant | VAV2 | GRCh38.p7 | 9:133767482 | CTGGATCTGGGAAAG[A/G]GCCCAGGTATGTGCT | 7410 |
rs7856935 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | VAV2 | GRCh38.p7 | 9:133971198 | CCAAAGCTTGCAGAT[A/G]GAACAGTCGTAACTG | 7410 |
rs7857083 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | VAV2 | GRCh38.p7 | 9:133825911 | TTCTACATTTTATGC[A/G]CCCTAAAAAATTATC | 7410 |
rs7858929 | snp | C/T | 0.208169 | 0.246476 | intron-variant | VAV2 | GRCh38.p7 | 9:133925513 | atgagccactgtacc[C/T]ggtcACAGTAATGTT | 7410 |
rs7858954 | snp | A/T | 0.238171 | 0.24972 | intron-variant | VAV2 | GRCh38.p7 | 9:133925578 | GCTCCAGCCCCAAAG[A/T]CCCCAGGGGCAGAGT | 7410 |
rs7859202 | snp | G/T | 0.395635 | 0.2032 | intron-variant | VAV2 | GRCh38.p7 | 9:133895643 | caggggctggggaaa[G/T]ttgggggggatgagg | 7410 |
rs7859372 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | VAV2 | GRCh38.p7 | 9:133805952 | TCAACAAGGGAGGAC[A/G]GGGTCCAGAGGGGGC | 7410 |
rs7859418 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133895803 | ggtgtgtcaactgca[C/T]ctcaacaatgctgct | 7410 |
rs7859624 | snp | G/T | 0.393065 | 0.205018 | intron-variant | VAV2 | GRCh38.p7 | 9:133868360 | GAGATGCTCTGCGAA[G/T]GGGGAAGAGCCCAGA | 7410 |
rs7859728 | snp | C/G | 0.0146672 | 0.084371 | utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133763052 | TTGAGTCGCCCGAGG[C/G]CCAGTTTGTAGGCTG | 7410 |
rs7859853 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | VAV2 | GRCh38.p7 | 9:133949708 | CGGAGGCATGGATTC[A/G]AAATGTCTGCTACCA | 7410 |
rs7860247 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133950009 | GACCAGCAGCCGTGA[A/T]GTCCAGGAACCCCAG | 7410 |
rs7860383 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV2 | GRCh38.p7 | 9:133845413 | GCTGGGGTGGGAGGG[C/T]CAGAATGGGGGGCCG | 7410 |
rs7863169 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | VAV2 | GRCh38.p7 | 9:133861674 | CGGCTCCTGTGGCCA[C/T]GCTGCTAACAACTCC | 7410 |
rs7863294 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | VAV2 | GRCh38.p7 | 9:133954799 | gtgcatgctcatgat[A/G]tatgtaccagtgtat | 7410 |
rs7863767 | snp | A/G | 0.21875 | 0.248039 | intron-variant | VAV2 | GRCh38.p7 | 9:133799900 | AAGACACTGACTCCC[A/G]GCGGCCGCCTGCACC | 7410 |
rs7864007 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133950153 | CTGCCCAGCAACCCC[G/T]GGCACAGGCAGGCAG | 7410 |
rs7864124 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133950220 | TGACGGTCAAGTCCT[C/T]CCTCAGCAGCACTCG | 7410 |
rs7864260 | snp | C/T | 0.436834 | 0.166111 | intron-variant | VAV2 | GRCh38.p7 | 9:133886632 | GACAAGAAAACAAGA[C/T]GGGCCCAGAGACAGC | 7410 |
rs7865299 | snp | A/G | 0.349046 | 0.229543 | synonymous-codon | VAV2 | GRCh38.p7 | 9:133797806 | CTCCCCGTAGATCAG[A/G]AGCCTGGACGGTGCA | 7410 |
rs7867413 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | VAV2 | GRCh38.p7 | 9:133890460 | TTGGGAGAGCAGAAA[A/T]GGGAAAAGTGCCGAG | 7410 |
rs7867588 | snp | A/G | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133895791 | ggcgaaccccatggt[A/G]tgtcaactgcatctc | 7410 |
rs7869252 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | VAV2 | GRCh38.p7 | 9:133840692 | ATTACGGGGCACCTG[C/T]GTGGGGCTGGCATGG | 7410 |
rs7869522 | snp | A/G | 0.359152 | 0.224913 | intron-variant | VAV2 | GRCh38.p7 | 9:133881968 | GCCAGGTGCCCAGCG[A/G]GTGTGCGGGGCTACA | 7410 |
rs7871847 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | VAV2 | GRCh38.p7 | 9:133864493 | GGCAGCCCTGGCTCC[A/G]TCCCCACCCAACCAT | 7410 |
rs7872213 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133950042 | CTGGGGCTCCCACCC[A/G]CTGCCAGGGTCTGTC | 7410 |
rs7872604 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | VAV2 | GRCh38.p7 | 9:133950337 | TTCAACTCTGCACCC[C/G]CCTCCAGTCCACAGT | 7410 |
rs7874428 | snp | A/C | 0.227369 | 0.248974 | intron-variant | VAV2 | GRCh38.p7 | 9:133900206 | cctgtctcaaaaaaa[A/C]caaagaagaaagaaa | 7410 |
rs7874464 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133806448 | ACGCAGCGGCCGACT[C/T]GGGGCGGGCTCTGCA | 7410 |
rs7874490 | snp | A/G | 0.084364 | 0.187256 | intron-variant | VAV2 | GRCh38.p7 | 9:133814758 | AAAGGCCCCCATGCC[A/G]CCCCCATCACAGGTC | 7410 |
rs7874587 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133900363 | cattctcccctggag[C/G]tggccatagaaacta | 7410 |
rs7875729 | snp | A/C | 0.234982 | 0.249549 | intron-variant | VAV2 | GRCh38.p7 | 9:133925368 | attacaggtgggtgc[A/C]actacatcctgctaa | 7410 |
rs7875782 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV2 | GRCh38.p7 | 9:133864746 | GGTAACGCCACAGAC[G/T]GGGTCAAAGCCTGCG | 7410 |
rs7875953 | snp | A/G/T | 0.0187101 | 0.0948959 | missense, synonymous-codon | VAV2 | GRCh38.p7 | 9:133775000 | GTAGGTCCCGCTGGC[A/G/T]TGGGACTTGAGCAGG | 7410 |
rs9409860 | snp | A/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133766759 | cttaaagtataaata[A/T]atatatatatatata | 7410 |
rs9409862 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV2 | GRCh38.p7 | 9:133776670 | TTTGTGACCCTTGTC[C/T]TCCCCTGCCGCCTGG | 7410 |
rs9409863 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | VAV2 | GRCh38.p7 | 9:133778117 | CTCAGCGTGTCAAGA[A/G]AAGGGCAAATGTGCC | 7410 |
rs9409864 | snp | A/G | 0.274929 | 0.248754 | intron-variant, utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133782344 | CGACCACGAGAGGGC[A/G]GTATTGATGGGCACA | 7410 |
rs9409865 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | VAV2 | GRCh38.p7 | 9:133801096 | CCAGCCCGGAGCCTG[C/T]CTGCACCAGGCACTC | 7410 |
rs9409867 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | VAV2 | GRCh38.p7 | 9:133836918 | TGAAGCCCAGCGCAG[C/G]GTTCTTAACACAGGG | 7410 |
rs9409868 | snp | C/G | 0.426507 | 0.177046 | intron-variant | VAV2 | GRCh38.p7 | 9:133890173 | CATCCACAGGGCACA[C/G]AGCCCTCCACACAGC | 7410 |
rs9657700 | snp | C/T | 0.310878 | 0.242475 | intron-variant | VAV2 | GRCh38.p7 | 9:133872210 | CGTCAGTGACCTGGC[C/T]GACCCCAAGAGGGAA | 7410 |
rs9657701 | snp | C/T | 0.268452 | 0.249318 | intron-variant | VAV2 | GRCh38.p7 | 9:133872322 | CACCCACGTCCTCCA[C/T]GTTTCCATGGCTGTG | 7410 |
rs9695613 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133899965 | ggcggagcttgcagt[A/G]agccgagattgcacc | 7410 |
rs9696103 | snp | C/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133899969 | gagcttgcagtgagc[C/G]gagattgcaccactg | 7410 |
rs9722384 | snp | A/G | 0.085476 | 0.188233 | synonymous-codon | VAV2 | GRCh38.p7 | 9:133768484 | GCCCTGGTCTCCGCC[A/G]ATGCGGCTGTAGATC | 7410 |
rs9792512 | snp | C/T | 0.249038 | 0.249998 | intron-variant | VAV2 | GRCh38.p7 | 9:133898812 | GGGAGGATGCAGACC[C/T]TGCCttttttttttt | 7410 |
rs9792513 | snp | C/T | 0.130008 | 0.219321 | intron-variant | VAV2 | GRCh38.p7 | 9:133899056 | tcgatctcctgacct[C/T]gtgatccgcccgcct | 7410 |
rs9792581 | snp | C/T | 0.227369 | 0.248974 | intron-variant | VAV2 | GRCh38.p7 | 9:133899444 | gatggggtctcgctc[C/T]gtcacccaggctgga | 7410 |
rs10114092 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | VAV2 | GRCh38.p7 | 9:133915498 | TGCCCACTTTACAAA[A/G]CACCCTGAAAACAGG | 7410 |
rs10114118 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | VAV2 | GRCh38.p7 | 9:133915586 | TCTCAAAGACAAGGC[A/G]CACACACACACACTC | 7410 |
rs10114138 | snp | A/C | 0.268995 | 0.249277 | intron-variant | VAV2 | GRCh38.p7 | 9:133872520 | CTCGGCTTGAAGGGT[A/C]GGGGTCCTAGGCCCA | 7410 |
rs10114514 | snp | C/T | 0.271702 | 0.249056 | intron-variant | VAV2 | GRCh38.p7 | 9:133868020 | GCCCCAAGTGCACCT[C/T]GGACAGACAGACCAG | 7410 |
rs10114577 | snp | C/T | 0.211516 | 0.24702 | intron-variant | VAV2 | GRCh38.p7 | 9:133906197 | GGCTCTGTGGGGACC[C/T]TCAAACATCCCTGCA | 7410 |
rs10114727 | snp | A/G | 0.149665 | 0.228982 | intron-variant | VAV2 | GRCh38.p7 | 9:133866579 | gagaccaaggtgggc[A/G]gatcactcgaggtca | 7410 |
rs10115680 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | VAV2 | GRCh38.p7 | 9:133975070 | GCCTTTTCCTGCTGA[C/T]GCCAACCAAGGCAGG | 7410 |
rs10116085 | snp | C/T | 0.29278 | 0.246313 | intron-variant | VAV2 | GRCh38.p7 | 9:133872780 | TGGGAGCTTCTTGAC[C/T]AAGACAGAGTCTACC | 7410 |
rs10116143 | snp | A/G | 0.188631 | 0.242351 | intron-variant | VAV2 | GRCh38.p7 | 9:133878204 | GCAGGCACCTCTGCT[A/G]ACATGTGGCAGCCAG | 7410 |
rs10116423 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | VAV2 | GRCh38.p7 | 9:133915428 | CTTTCTCCCAAGGAG[C/T]ACAGGTGGTGCAATG | 7410 |
rs10116617 | snp | C/T | 0.105569 | 0.204058 | intron-variant | VAV2 | GRCh38.p7 | 9:133851161 | GTGCCACATGGCCTC[C/T]ACCACGCACTCAGGA | 7410 |
rs10117330 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | VAV2 | GRCh38.p7 | 9:133919712 | AAACAGCGCAGAGAG[C/T]GGGGCCAGATGGACG | 7410 |
rs10118332 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | VAV2 | GRCh38.p7 | 9:133801118 | CAGGCACTCACACAC[A/G]GCTGTGAGTGGCCAC | 7410 |
rs10118439 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | VAV2 | GRCh38.p7 | 9:133877642 | GCCTCAGCCTCCCGA[C/T]TGAGCCTCACCCCAG | 7410 |
rs10119331 | snp | C/G | 0.46845 | 0.121572 | intron-variant | VAV2 | GRCh38.p7 | 9:133796698 | AGGTGTGTGCAGAGG[C/G]GGGGGCTTCACAACA | 7410 |
rs10119727 | snp | A/G | 0.44768 | 0.153045 | intron-variant | VAV2 | GRCh38.p7 | 9:133963246 | ATCAATTAATGATCA[A/G]TCAATCAGGGATCGG | 7410 |
rs10119757 | snp | A/G | 0.44755 | 0.153212 | intron-variant | VAV2 | GRCh38.p7 | 9:133963353 | AGGGAGAGAGGGCAC[A/G]GAGGCCATCAAGCAG | 7410 |
rs10120042 | snp | A/G | 0.172674 | 0.237741 | intron-variant | VAV2 | GRCh38.p7 | 9:133803131 | TCGTTCCAGGATTCC[A/G]AGTGGAAGTCTCGGT | 7410 |
rs10120426 | snp | A/G | 0.447291 | 0.153545 | intron-variant | VAV2 | GRCh38.p7 | 9:133963501 | CAGCAGGGTCCAGTC[A/G]TGCCGACAGGCAGCT | 7410 |
rs10120521 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | VAV2 | GRCh38.p7 | 9:133808608 | TCTGGTCACTAGGCC[A/G]GGCCATGCCTTGTGC | 7410 |
rs10120683 | snp | C/T | 0.297382 | 0.245469 | intron-variant | VAV2 | GRCh38.p7 | 9:133986254 | gatgcagcgtggagg[C/T]ggagctagaccccta | 7410 |
rs10121278 | snp | C/T | 0.49334 | 0.057322 | intron-variant | VAV2 | GRCh38.p7 | 9:133794261 | GGGCGGCTTGGGGGC[C/T]GCAGAGCTGACACCG | 7410 |
rs10123394 | snp | C/T | 0.223225 | 0.248562 | intron-variant | VAV2 | GRCh38.p7 | 9:133801438 | CATGGCTCTCAACCC[C/T]GGCCCTCAGGGCCCC | 7410 |
rs10123623 | snp | A/G | 0.323434 | 0.238972 | intron-variant | VAV2 | GRCh38.p7 | 9:133803033 | TTGAGGTGGACCATG[A/G]CCGGGGACTCTCCCT | 7410 |
rs10123766 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | VAV2 | GRCh38.p7 | 9:133912960 | CACGGGCGGTGGAGT[A/G]CCATTTGGAACCGGG | 7410 |
rs10123947 | snp | C/T | 0.291235 | 0.246576 | intron-variant | VAV2 | GRCh38.p7 | 9:133905304 | agccgggcgtggtgg[C/T]gggcacctgtagtcc | 7410 |
rs10124419 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV2 | GRCh38.p7 | 9:133970949 | CAGGCCAATTTCTCC[C/T]AAGGTTCATTTGCAT | 7410 |
rs10125207 | snp | A/G | 0.115088 | 0.210473 | intron-variant | VAV2 | GRCh38.p7 | 9:133919759 | AGCAACACAAACAGC[A/G]CATTCTTGGCATCCG | 7410 |
rs10125572 | snp | A/G/T | 0.0803491 | 0.183626 | intron-variant | VAV2 | GRCh38.p7 | 9:133915098 | GGCCGGAAGAGCACC[A/G/T]GCCTGTTCTCCATTA | 7410 |
rs10125709 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | VAV2 | GRCh38.p7 | 9:133904513 | GGACGGCAAATGCAC[G/T]TGCAGGAAAGCAGCC | 7410 |
rs10217159 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | VAV2 | GRCh38.p7 | 9:133868219 | AACTGCTGTGAGCTA[C/T]CCGGGGCTCGGGTCT | 7410 |
rs10217798 | snp | A/G | 0.270621 | 0.249148 | intron-variant | VAV2 | GRCh38.p7 | 9:133870732 | ACAGACGGATGGATC[A/G]GCAGATGAGTGGACA | 7410 |
rs10530876 | in-del | -/AT | 0.420733 | 0.18262 | intron-variant | VAV2 | GRCh38.p7 | 9:133964310 | CTGCAGTGAGCCCTG[-/AT]ATATATATATATACA | 7410 |
rs10538806 | in-del | -/ATTT | | | intron-variant | VAV2 | GRCh38.p7 | 9:133900767 | CTACCTCCTGTCTTG[-/ATTT]ATTTATTTATTTATT | 7410 |
rs10539965 | in-del | -/TGCA | 0.239614 | 0.249784 | intron-variant | VAV2 | GRCh38.p7 | 9:133938510 | CACCAGCCCGGCTCC[-/TGCA]TGCAGGACTGGTGCC | 7410 |
rs10541639 | in-del | -/AT | | | intron-variant | VAV2 | GRCh38.p7 | 9:133964023 | AAAAATTATTCATTC[-/AT]ATATATATATATATA | 7410 |
rs10555726 | in-del | -/A | 0.5 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133926015 | CTGCGGACATGGACC[-/A]AAAAAAAAAAAAAAA | 7410 |
rs10561589 | in-del | -/CCAG | 0.249886 | 0.25 | intron-variant | VAV2 | GRCh38.p7 | 9:133824437 | ATAGAAGAGACCCAG[-/CCAG]GACACTCTTAAAACC | 7410 |
rs10599176 | in-del | -/A | | | intron-variant | VAV2 | GRCh38.p7 | 9:133832572 | TTCTTTTTTTTTTTT[-/A]CCCCAGACGGAGTTT | 7410 |
rs10634807 | in-del | -/CT | 0.0146672 | 0.084371 | intron-variant | VAV2 | GRCh38.p7 | 9:133964541 | AATTATAGGCCAATA[-/CT]CCCTAACGAACATAG | 7410 |
rs10673098 | in-del | -/GTGA | 0.463018 | 0.130857 | intron-variant | VAV2 | GRCh38.p7 | 9:133954777 | CATGTGTGTGCACAT[-/GTGA]GTATGTGTGCATGCT | 7410 |
rs10710216 | in-del | -/T | 0.0810805 | 0.184299 | intron-variant | VAV2 | GRCh38.p7 | 9:133810055 | AGGGTCTCTGATGCC[-/T]GAAGTCATGTGTGCC | 7410 |
rs10739995 | snp | A/G | 0.372995 | 0.217652 | intron-variant | VAV2 | GRCh38.p7 | 9:133876227 | TATCCATATGCTATC[A/G]GCGCTGCTGTTCTGG | 7410 |
rs10761399 | snp | A/G | 0.499987 | 0.00259581 | intron-variant | VAV2 | GRCh38.p7 | 9:133791261 | CCTCTGCAGGGCCAG[A/G]CTCTGGGGAGCCCCA | 7410 |
rs10821524 | snp | A/C | 0.492386 | 0.0612297 | intron-variant | VAV2 | GRCh38.p7 | 9:133789431 | GACTGTCGTGCACCC[A/C]AGGGAACTCCCCACA | 7410 |
rs10821525 | snp | A/G | 0.404035 | 0.196909 | intron-variant | VAV2 | GRCh38.p7 | 9:133797516 | GTCCTGGCCTGGGAT[A/G]GTGACCTCCACCCAA | 7410 |
rs10821526 | snp | C/T | 0.36955 | 0.219562 | intron-variant | VAV2 | GRCh38.p7 | 9:133846443 | CACTCTGGAGCCCCT[C/T]GAGGCCAGGCAGGGC | 7410 |
rs10821527 | snp | C/T | 0.392696 | 0.205275 | intron-variant | VAV2 | GRCh38.p7 | 9:133868853 | AGTGACCCAGAACAA[C/T]GACCCAGGTGGATGC | 7410 |
rs10821528 | snp | C/T | 0.322959 | 0.239117 | intron-variant | VAV2 | GRCh38.p7 | 9:133868924 | CTCATGCCTGTAATC[C/T]CAGCTACAGCCTCAC | 7410 |
rs10821529 | snp | A/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133870889 | GTGGGTGGATGGATA[A/T]GGGTGAGTGCGTGGG | 7410 |
rs10821530 | snp | A/G | 0.21695 | 0.247806 | intron-variant | VAV2 | GRCh38.p7 | 9:133871172 | TGGGCAGATGGATGG[A/G]TAGATGAGTGGGTGG | 7410 |
rs10821531 | snp | A/G/T | 0.315273 | 0.241329 | intron-variant | VAV2 | GRCh38.p7 | 9:133871440 | GATGGATGGATTGAT[A/G/T]GATGGATGGATGGAT | 7410 |
rs10821532 | snp | A/G | 0.26818 | 0.249338 | intron-variant | VAV2 | GRCh38.p7 | 9:133871468 | GATGGATGGAGAAGC[A/G]GATGGATGGATGGAT | 7410 |
rs10821533 | snp | A/G | 0.245346 | 0.249957 | intron-variant | VAV2 | GRCh38.p7 | 9:133885358 | GTTCAAGGTCGGTGT[A/G]CTCAGGCATCCCTGT | 7410 |
rs10821534 | snp | C/G | 0.230896 | 0.249269 | intron-variant | VAV2 | GRCh38.p7 | 9:133900604 | GCGCGGCTCAGAGAG[C/G]CCAGTAAGAATCCAG | 7410 |
rs10821535 | snp | C/T | 0.227074 | 0.248947 | intron-variant | VAV2 | GRCh38.p7 | 9:133900726 | ATAAATGTTCAATCG[C/T]CTTGCCTTTTCTCCA | 7410 |
rs10821536 | snp | C/T | 0.172997 | 0.237846 | intron-variant | VAV2 | GRCh38.p7 | 9:133904423 | TGTCCTCCAGGGTCC[C/T]GTGAAATTCAAACCA | 7410 |
rs10821538 | snp | A/C | 0.0821764 | 0.185298 | intron-variant | VAV2 | GRCh38.p7 | 9:133922613 | AAGAATCATCGTTCC[A/C]ACACATGGTGCTGGG | 7410 |
rs10821540 | snp | C/T | 0.5 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133952895 | AACCTGGAGGGAGCA[C/T]GGCCCCACTGACACC | 7410 |
rs10821542 | snp | A/G | 0.325091 | 0.238456 | intron-variant | VAV2 | GRCh38.p7 | 9:133972655 | TCGGCAGGGCCTCCC[A/G]CAAGAGTCCTCACAA | 7410 |
rs10993795 | snp | A/G | 0.0611083 | 0.163768 | utr-variant-3-prime | VAV2 | GRCh38.p7 | 9:133763793 | AGCCTGGCTCGCAGC[A/G]CTGTCGGTGCCCCCT | 7410 |
rs10993796 | snp | G/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133773889 | TCTATATGACTGGCA[G/T]CACTGTAGGTTTGTT | 7410 |
rs10993797 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | VAV2 | GRCh38.p7 | 9:133779487 | TGTACTGAGCACTGC[C/G]TGGACTGCACTCAAG | 7410 |
rs10993798 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | VAV2 | GRCh38.p7 | 9:133779584 | AAGGCAGGAAGGGGA[C/T]GGAGAACGTGGTGGG | 7410 |
rs10993799 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | VAV2 | GRCh38.p7 | 9:133779768 | GAGGCCAGAGAGGCA[A/G]GAGGGAGGGGGCCCA | 7410 |
rs10993800 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | VAV2 | GRCh38.p7 | 9:133789138 | CAACACAAAGCCACC[A/G]CCAGGCAGCTCTTTC | 7410 |
rs10993802 | snp | A/G | 0.499891 | 0.00738737 | intron-variant | VAV2 | GRCh38.p7 | 9:133792582 | GTGTCTGACTGTGTG[A/G]TTGTGTGTGTGAGCA | 7410 |
rs10993803 | snp | C/T | 0.493477 | 0.0567349 | intron-variant | VAV2 | GRCh38.p7 | 9:133793865 | CAAGCCCAGGTACAG[C/T]GACGACTCCCATAGT | 7410 |
rs10993805 | snp | A/C/G | 0.22431 | 0.263689 | intron-variant | VAV2 | GRCh38.p7 | 9:133802030 | CACACAGACGCCTTC[A/C/G]CCCTCCGTCCACACC | 7410 |
rs10993807 | snp | A/C | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133814947 | TTGCACTGCCATTTA[A/C]TGAGGACTCTACGAC | 7410 |
rs10993808 | snp | G/T | 0.475437 | 0.108066 | intron-variant | VAV2 | GRCh38.p7 | 9:133818173 | atcgagaccatcctg[G/T]ctaacatgatgaaaa | 7410 |
rs10993809 | snp | C/T | 0.232359 | 0.249377 | intron-variant | VAV2 | GRCh38.p7 | 9:133818282 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 7410 |
rs10993810 | snp | A/G | 0.308908 | 0.242961 | intron-variant | VAV2 | GRCh38.p7 | 9:133818634 | CAGGCAGCATATGGC[A/G]GGACTTTCTGGCCTC | 7410 |
rs10993811 | snp | C/T | 0.319856 | 0.240042 | intron-variant | VAV2 | GRCh38.p7 | 9:133818686 | CCATAATAAATCCCC[C/T]CAGCCATCTACAGAG | 7410 |
rs10993812 | snp | A/G | 0.319856 | 0.240042 | intron-variant | VAV2 | GRCh38.p7 | 9:133818730 | TGCTTCTTGGAAGCC[A/G]CTAATTGCAACATCT | 7410 |
rs10993813 | snp | A/G | 0.286303 | 0.24735 | intron-variant | VAV2 | GRCh38.p7 | 9:133819241 | cgaggtcaggagatc[A/G]agaccatcctggcta | 7410 |
rs10993814 | snp | A/G | 0.302184 | 0.244493 | intron-variant | VAV2 | GRCh38.p7 | 9:133820449 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 7410 |
rs10993815 | snp | C/T | 0.303187 | 0.244277 | intron-variant | VAV2 | GRCh38.p7 | 9:133820686 | CAGTCACCTGGAAGG[C/T]AGGTTCACTTACGTC | 7410 |
rs10993816 | snp | C/T | 0.189576 | 0.242588 | intron-variant | VAV2 | GRCh38.p7 | 9:133829638 | GTTAACTATAACATA[C/T]ATTTTTTTTTTTAAG | 7410 |
rs10993817 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133832517 | AGTCCCTCAGTCAGT[C/T]TCAGAAGCCTGCATG | 7410 |
rs10993818 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | VAV2 | GRCh38.p7 | 9:133839072 | TGGATGGGCGAGTGG[C/T]TGGATGAATGGCTAG | 7410 |
rs10993819 | snp | C/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133841591 | CATGCAGCTCCCAGG[C/T]TCCGTCCCCAAACAC | 7410 |
rs10993820 | snp | A/G | 0.275197 | 0.248727 | intron-variant | VAV2 | GRCh38.p7 | 9:133842608 | ATTTATGGTGCTGAC[A/G]CTATCGGGGGGTGGT | 7410 |
rs10993821 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV2 | GRCh38.p7 | 9:133847350 | CGGGACCTTGCACCG[C/T]GCCTCAGCGTGAGCA | 7410 |
rs10993822 | snp | A/G | 0.202651 | 0.245475 | intron-variant | VAV2 | GRCh38.p7 | 9:133849087 | GAAGAGGCGGCCTTG[A/G]TTTGTTTTGCTTGTT | 7410 |
rs10993823 | snp | A/G | 0.161596 | 0.233848 | intron-variant | VAV2 | GRCh38.p7 | 9:133851427 | CTCCAAAGGGCCGGT[A/G]AGGACACTGAGGTTC | 7410 |
rs10993824 | snp | A/T | 0.161596 | 0.233848 | intron-variant | VAV2 | GRCh38.p7 | 9:133851435 | GGCCGGTGAGGACAC[A/T]GAGGTTCAGGGTGTA | 7410 |
rs10993825 | snp | G/T | 0.233527 | 0.249457 | intron-variant | VAV2 | GRCh38.p7 | 9:133852179 | gggtgggtagatgta[G/T]cgatgaggggacgga | 7410 |
rs10993826 | snp | G/T | 0.183886 | 0.241099 | intron-variant | VAV2 | GRCh38.p7 | 9:133853923 | TTCAGACTCAACTGT[G/T]GGAGATACTGGGATA | 7410 |
rs10993827 | snp | C/T | | | intron-variant | VAV2 | GRCh38.p7 | 9:133854129 | ccttgcacctgcaca[C/T]acacaccccttgcac | 7410 |
rs10993828 | snp | A/C | 0.201727 | 0.245295 | intron-variant | VAV2 | GRCh38.p7 | 9:133856546 | TAGCTGGGCCTTCAG[A/C]CAGCCTCCCAGCCAA | 7410 |
rs10993829 | snp | C/T | 0.253824 | 0.249971 | intron-variant | VAV2 | GRCh38.p7 | 9:133856619 | TGGAGAGTTGGTGGC[C/T]TCAAGCAACACAGAC | 7410 |
rs10993830 | snp | C/G | 0.269267 | 0.249256 | intron-variant | VAV2 | GRCh38.p7 | 9:133856700 | TCAAGGTATCGAGGG[C/G]CTGGTCCCTTTCAGG | 7410 |
rs10993831 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | VAV2 | GRCh38.p7 | 9:133857236 | TAGCTCTGGCCACAG[C/T]AAGACCCACATCCCC | 7410 |
rs10993832 | snp | A/C | 0.305436 | 0.243776 | intron-variant | VAV2 | GRCh38.p7 | 9:133858010 | CGTCTCTCATGTCTG[A/C]CTATCCTGTGTGCAG | 7410 |
rs10993833 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | VAV2 | GRCh38.p7 | 9:133865749 | AGTCTGGTAAACATA[C/T]ATATATTCACAGATT | 7410 |
rs10993834 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | VAV2 | GRCh38.p7 | 9:133868496 | gtaggtgaatgagAC[A/G]GAGCCTGGCCCAAAG | 7410 |
rs10993835 | snp | C/G | 0.460477 | 0.134905 | intron-variant | VAV2 | GRCh38.p7 | 9:133873654 | CTGGGCAAGCTGCAT[C/G]AGGCAGCTGCATCAG | 7410 |
rs10993836 | snp | A/G | 0.171057 | 0.237209 | intron-variant | VAV2 | GRCh38.p7 | 9:133873789 | GGTCCAAATTCTCCA[A/G]TTTTGAGATGGGAAA | 7410 |
rs10993837 | snp | C/T | 0.386313 | 0.209568 | intron-variant | VAV2 | GRCh38.p7 | 9:133874681 | TCTACACAGATGTCT[C/T]GCCCCCTCCAAGAAC | 7410 |
rs10993838 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | VAV2 | GRCh38.p7 | 9:133876424 | ACTATTCCCCTAAGG[A/C]AGGCAGGCCCCCTGG | 7410 |
rs10993839 | snp | A/G | 0.153665 | 0.230694 | intron-variant | VAV2 | GRCh38.p7 | 9:133879542 | TCAGTAGGTGGCCCC[A/G]GGGCACTGCCACAGC | 7410 |
rs10993840 | snp | C/T | 0 | 0 | intron-variant | VAV2 | GRCh38.p7 | 9:133880402 | GGGAAGGACAATGGC[C/T]TTAGGGGCAGCCATG | 7410 |
rs10993842 | snp | C/T | 0.184203 | 0.241186 | intron-variant | VAV2 | GRCh38.p7 | 9:133884588 | CAGGCTGTTACTTTA[C/T]GGAACATCAGCAAGC | 7410 |
rs10993843 | snp | C/T | 0.247337 | 0.249986 | intron-variant | VAV2 | GRCh38.p7 | 9:133896816 | AAAAATCCAACCAGG[C/T]GGGTACAGTGGCTCA | 7410 |
rs10993844 | snp | G/T | 0.342134 | 0.232404 | intron-variant | VAV2 | GRCh38.p7 | 9:133897229 | CTCGGGAAGAAAGCC[G/T]CTCCTTTGAGCAGCA | 7410 |
rs10993845 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | VAV2 | GRCh38.p7 | 9:133897678 | TTTCCAGATCGTCCA[C/T]GATTGCTCTTCTATG | 7410 |
rs10993846 | snp | C/T | 0.0898077 | 0.191933 | intron-variant | VAV2 | GRCh38.p7 | 9:133900473 | CTCTAACTGTCCCTC[C/T]ACCCTATCTGTATAA | 7410 |
rs10993847 | snp | A/G | | | intron-variant | VAV2 | GRCh38.p7 | 9:133901052 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 7410 |
rs10993848 | snp | C/T | 0.103438 | 0.202533 | intron-variant | VAV2 | GRCh38.p7 | 9:133901496 | gggagagccatggca[C/T]cacctcgagcctggt | 7410 |
rs10993849 | snp | A/G | 0.103794 | 0.20279 | intron-variant | VAV2 | GRCh38.p7 | 9:133901992 | CTTAGTGGTCTGCAC[A/G]TCAGGAGACTCTGTG | 7410 |