SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs369856 | snp | C/T | 0.437118 | 0.165792 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463343 | TCTAAGTAATTCATA[C/T]TGATAATGGCATTTT | 23062 |
rs488131 | snp | A/G | 0.291493 | 0.246533 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463819 | CTGCCACGCCCAGCT[A/G]ATGTTGCAGTTTTTC | 23062 |
rs494279 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467315 | ACTGTAGCAGAGATG[A/G]TGATGATGAGAAATG | 23062 |
rs722069 | snp | C/T | 0.455024 | 0.143057 | intron-variant | GGA2 | GRCh38.p7 | 16:23495619 | CTTTGTCTCTCAAGA[C/T]TGTTTTAGGGTTAAG | 23062 |
rs727238 | snp | A/G | 0.420733 | 0.18262 | intron-variant | GGA2 | GRCh38.p7 | 16:23509745 | CGTATATATATATAT[A/G]TGTGTTTTTTTTTTC | 23062 |
rs739498 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | GGA2 | GRCh38.p7 | 16:23505353 | CTGTTTTTAATAGCG[C/T]AAGGCTAGCAACACC | 23062 |
rs867131 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | GGA2 | GRCh38.p7 | 16:23505979 | CATTAGGCTTTTATA[A/G]CTGCAAGTAATTGAA | 23062 |
rs1056961 | snp | C/T | 0 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464625 | CATTTGGCCTGTTTT[C/T]TAAATAATCCCACAT | 23062 |
rs1056962 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464531 | GCCTCTGTCCCAATT[C/T]TGAGTAACAGCTCTG | 23062 |
rs1071685 | snp | C/G | 0.375601 | 0.216158 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510322 | GCTGGAGCTGTGGCT[C/G]AGTGAGTAGCCTGGC | 23062 |
rs1135045 | snp | C/G | 0.368479 | 0.220142 | missense | GGA2 | GRCh38.p7 | 16:23478390 | CTGGACCTCCTCTCA[C/G]CACAGCCAGCTCCGT | 23062 |
rs1135088 | snp | C/G | 0.0562307 | 0.157967 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465892 | gtgcggtggtataat[C/G]tcagctcactgcaat | 23062 |
rs1141325 | snp | A/G | 0 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465260 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT | 23062 |
rs1427880 | snp | A/C | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23506506 | TCACCAGATACTGCC[A/C]TGTTTCCCCAGGGTT | 23062 |
rs2040574 | snp | C/T | 0.279195 | 0.248289 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499005 | CTCCCCCTGTTCTCT[C/T]CCTGCCTCTGCTCTT | 23062 |
rs2097662 | snp | G/T | 0.429238 | 0.174281 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512024 | agcacaaccttccag[G/T]ttctagcctttcttt | 23062 |
rs2239951 | snp | A/G | 0.428333 | 0.175206 | intron-variant | GGA2 | GRCh38.p7 | 16:23493672 | TAAGCTATTTCCTGG[A/G]CATAAACCTCAGGCA | 23062 |
rs2285521 | snp | A/G | 0.472318 | 0.114344 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510459 | CCAGGACGCTACAGC[A/G]GCTGAAGAGGCAGTG | 23062 |
rs2285522 | snp | A/G | 0.416322 | 0.186646 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510429 | GGCGCCCGCGGCCGC[A/G]GCGTCGGGGCTGGAG | 23062 |
rs2369012 | snp | C/T | 0.429688 | 0.173817 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504013 | GCTCACCGCAACCTC[C/T]GTCTCCCGGGTTCAA | 23062 |
rs2369013 | snp | A/G | 0.447032 | 0.153878 | intron-variant | GGA2 | GRCh38.p7 | 16:23485025 | ttccattgtgtggct[A/G]tgccacagtttgttt | 23062 |
rs3208913 | snp | C/T | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23494016 | GGCAAGTTCATGTGC[C/T]TTTTCTAGAGAGGGC | 23062 |
rs3785408 | snp | A/G | 0.279726 | 0.248226 | intron-variant | GGA2 | GRCh38.p7 | 16:23508665 | GAGCAGAGGTTTGGA[A/G]AGAGAGCGTGGGGAG | 23062 |
rs4018195 | in-del | -/TG | 0.34437 | 0.231505 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466677 | TAAGATGGGAAACTG[-/TG]NGTACAGATAGACAT | 23062 |
rs4115667 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466724 | TGATGAATCGGCCAA[A/C]AGCCAGCCCTTGCCA | 23062 |
rs4332751 | snp | A/G | 0.184203 | 0.241186 | intron-variant | GGA2 | GRCh38.p7 | 16:23490463 | TCCACagccgggagc[A/G]gtggctcacgcctgt | 23062 |
rs4558420 | snp | C/T | 0.44755 | 0.153212 | intron-variant | GGA2 | GRCh38.p7 | 16:23484147 | gcacagtggctcaca[C/T]ctgtaatcccagcac | 23062 |
rs4967955 | snp | C/G | 0.269809 | 0.249214 | intron-variant | GGA2 | GRCh38.p7 | 16:23471202 | GTCTCTTTTATATGA[C/G]TACAAACACACACAT | 23062 |
rs4967956 | snp | A/G | 0.437824 | 0.164991 | intron-variant | GGA2 | GRCh38.p7 | 16:23477704 | gtgagctgagatcgc[A/G]ccactgcactccacc | 23062 |
rs4967957 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | GGA2 | GRCh38.p7 | 16:23494671 | GCCCAGTCCCATGAG[C/T]AGCCACAGCAGCACA | 23062 |
rs4968005 | snp | A/G | 0.178785 | 0.239642 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467214 | GTGGATGAATGGAAC[A/G]AACGATACATGAAAA | 23062 |
rs4968006 | snp | A/G | 0.337158 | 0.234315 | intron-variant | GGA2 | GRCh38.p7 | 16:23476710 | TACAAAAAAAGCAAA[A/G]AAGGAACGTTCAACC | 23062 |
rs4968007 | snp | A/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23478208 | CGTCTCAAAAAAAAA[A/G]AAAAAAGAAAAAAAG | 23062 |
rs4968008 | snp | G/T | 0.356402 | 0.226275 | intron-variant | GGA2 | GRCh38.p7 | 16:23479032 | AAATAAGCAACTTAC[G/T]GAAGGTCATGTGACT | 23062 |
rs4968010 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | GGA2 | GRCh38.p7 | 16:23481144 | agcattttgggaggc[C/T]gaggcgggtggatca | 23062 |
rs4968011 | snp | C/T | 0.29175 | 0.246489 | intron-variant | GGA2 | GRCh38.p7 | 16:23489237 | TGTGCAAATTCACAA[C/T]ATTTTTGTTGTTTTT | 23062 |
rs4968013 | snp | G/T | 0.27893 | 0.24832 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501271 | TGGTAGCATCGCTCT[G/T]TGTCCTACTAATTGG | 23062 |
rs5816214 | in-del | -/C | 0.279726 | 0.248226 | intron-variant | GGA2 | GRCh38.p7 | 16:23506893 | TCTGTGAGGCCAGGT[-/C]CCCCCTTTTTGCTCT | 23062 |
rs6497664 | snp | C/G | 0.447162 | 0.153712 | intron-variant | GGA2 | GRCh38.p7 | 16:23474032 | CCTGAGTTGTGTCCT[C/G]CTCTGCATACTGGTG | 23062 |
rs6497666 | snp | C/T | 0.287606 | 0.247155 | intron-variant | GGA2 | GRCh38.p7 | 16:23484356 | ccgggaggcagaagt[C/T]gtgcggagctgagat | 23062 |
rs7185600 | snp | C/T | 0.447032 | 0.153878 | intron-variant | GGA2 | GRCh38.p7 | 16:23477568 | ctaacacagtgaaac[C/T]ccatctctactaaaa | 23062 |
rs7190131 | snp | C/T | 0.428937 | 0.17459 | intron-variant | GGA2 | GRCh38.p7 | 16:23490828 | TATTTTATGTCTGCA[C/T]GTTGTTACTTTTATC | 23062 |
rs7202661 | snp | A/C | 0.283947 | 0.247685 | intron-variant | GGA2 | GRCh38.p7 | 16:23492720 | agggaattatggaat[A/C]tggggcggtgggggt | 23062 |
rs7203580 | snp | A/G | 0.29432 | 0.24604 | intron-variant | GGA2 | GRCh38.p7 | 16:23492927 | cCCATGGCCAGCATC[A/G]GCACTGTTGTGGGAA | 23062 |
rs7204714 | snp | A/C | 0.324382 | 0.238678 | intron-variant | GGA2 | GRCh38.p7 | 16:23472032 | AGCAACCTTTTCAGA[A/C]GGGAAATTGGTAATG | 23062 |
rs8054517 | snp | A/G | 0.00673275 | 0.0576285 | intron-variant | GGA2 | GRCh38.p7 | 16:23483036 | TGGTTCATGACACAC[A/G]CCCAGGCACCCCATA | 23062 |
rs8061917 | snp | G/T | 0.0566069 | 0.158427 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501754 | GAAACAACAAAATTA[G/T]GATTTTCTTTTTTTG | 23062 |
rs9302410 | snp | C/T | 0.439641 | 0.162899 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500051 | AAGGAAGAGGAGCTC[C/T]CTCTGTGCTCTCTTC | 23062 |
rs9745351 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | GGA2 | GRCh38.p7 | 16:23472524 | TTTTAACAGCAAACA[A/G]GTAGAAAGAAATTGA | 23062 |
rs9927961 | snp | A/G | 0.428333 | 0.175206 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503204 | CCACTGTCGATTTGC[A/G]ATTTCCTCCTCCAAC | 23062 |
rs9928410 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | GGA2 | GRCh38.p7 | 16:23490510 | gaggctgaggcaggc[A/G]gatcatttgaggttg | 23062 |
rs9932261 | snp | C/T | 0.178785 | 0.239642 | intron-variant | GGA2 | GRCh38.p7 | 16:23509582 | GGAATATTCTTTATC[C/T]CCTTTGAACCTCAAT | 23062 |
rs9933261 | snp | A/G | 0.438526 | 0.164189 | intron-variant | GGA2 | GRCh38.p7 | 16:23504631 | AGCTGGGTCTGACCA[A/G]GCCACAGCAACCGCC | 23062 |
rs9936146 | snp | A/T | 0.188316 | 0.242271 | intron-variant | GGA2 | GRCh38.p7 | 16:23489408 | CCCAGGTAATTTTTT[A/T]AAAAAATTTTTTGTA | 23062 |
rs9938478 | snp | C/T | 0.166832 | 0.235761 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512124 | accatgtttgaaagg[C/T]ggaagaagagaccca | 23062 |
rs9939086 | snp | A/G | 0.184203 | 0.241186 | intron-variant | GGA2 | GRCh38.p7 | 16:23471800 | cattctagctacctg[A/G]gggtctgaggcagga | 23062 |
rs10153059 | snp | C/T | 0.436692 | 0.166271 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501062 | CATAAAGCACAGATA[C/T]GCAAATAGATCTCTG | 23062 |
rs10686275 | in-del | -/GAAA | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23475954 | AAAGAAAAAAACAAA[-/GAAA]AGCACTTAAAATGTC | 23062 |
rs10716091 | in-del | -/A | 0.0425829 | 0.139564 | intron-variant | GGA2 | GRCh38.p7 | 16:23497111 | TCCTGCCTCAAAAAC[-/A]AAAAAAAAAAACAAC | 23062 |
rs11074559 | snp | A/G | 0.374315 | 0.2169 | intron-variant | GGA2 | GRCh38.p7 | 16:23474876 | CCAGGGAAAAAAAAA[A/G]AAAGGTGGGGAGTGA | 23062 |
rs11074560 | snp | A/G | 0.42574 | 0.177808 | intron-variant | GGA2 | GRCh38.p7 | 16:23482035 | actttgggaagccga[A/G]gcagacggatcacta | 23062 |
rs11074561 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | GGA2 | GRCh38.p7 | 16:23484374 | gcggagctgagatca[C/T]gcaattgcactccag | 23062 |
rs11074562 | snp | A/G | 0.437401 | 0.165472 | intron-variant | GGA2 | GRCh38.p7 | 16:23488379 | AAGACCCAGGATGCA[A/G]TGTCTGCCTAAGAAC | 23062 |
rs11074563 | snp | C/G | 0.317451 | 0.240729 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511972 | aattattttgcattg[C/G]tatcaacttaacaga | 23062 |
rs11282065 | in-del | -/GCTGTCTACA | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511977 | TTTGCATTGGTATCA[-/GCTGTCTACA]ACTTAACAGAGTTAT | 23062 |
rs11540711 | snp | G/T | 0 | 0 | missense | GGA2 | GRCh38.p7 | 16:23474999 | CTAAGTCCTCTCCAG[G/T]TTGGTCCTGGGAGGC | 23062 |
rs11641480 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | GGA2 | GRCh38.p7 | 16:23493034 | GGACAAGGCAGGAGG[A/T]GATAGGAAACTTTCA | 23062 |
rs11644399 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497039 | gaagtggaaagactg[A/C]ggctgcagtgagcca | 23062 |
rs11645794 | snp | G/T | 0.00470586 | 0.0482782 | intron-variant | GGA2 | GRCh38.p7 | 16:23488825 | GCTAGCAAAGCACTG[G/T]CAACAGCCTTCAAAG | 23062 |
rs11647801 | snp | A/C | 0 | 0 | splice-donor-variant | GGA2 | GRCh38.p7 | 16:23494301 | AGGCAAGCCAAACTC[A/C]CCGTTAAGGCATAAA | 23062 |
rs11861353 | snp | A/C | 0.029116 | 0.117091 | intron-variant | GGA2 | GRCh38.p7 | 16:23508032 | TTTTATCTCCTCCAC[A/C]TGAGGCAGCTACTTT | 23062 |
rs11861512 | snp | A/C | 0.00655451 | 0.0568708 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474923 | CTTAACAGACTCCAA[A/C]GGGACAAACACTTGA | 23062 |
rs12325456 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470954 | cccacctcagcctcc[C/T]tagtagctgggatta | 23062 |
rs12598472 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23479996 | TCAAATGGTAACGCC[C/T]TCCCTGCCCTTCCAA | 23062 |
rs12920008 | snp | C/G | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23495396 | CCCCACATGAATTTG[C/G]TAATTTTAGAAAAAT | 23062 |
rs12921516 | snp | G/T | 0.42357 | 0.179927 | intron-variant | GGA2 | GRCh38.p7 | 16:23510082 | GTGCTGCTGCTAAGT[G/T]GGGGGGTGGGCGGAG | 23062 |
rs13330465 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509395 | GTGACGACCCCCAGG[A/T]AAACCAACTCCTACC | 23062 |
rs13331947 | snp | A/T | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23489586 | gatcacagggcaaca[A/T]ccaagtaacctgaaa | 23062 |
rs13334394 | snp | C/T | 0.179744 | 0.239925 | intron-variant | GGA2 | GRCh38.p7 | 16:23496682 | aaaattaagaccagg[C/T]gcgatggctcacgcc | 23062 |
rs13337568 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | GGA2 | GRCh38.p7 | 16:23486406 | AAGTCCTCTGAAAAG[C/T]AGATTCCTAAACCTG | 23062 |
rs16940153 | snp | C/G | 0.0142736 | 0.0832652 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466910 | AGGAACTCTGTCCAG[C/G]GGCGATTCTAAGGCA | 23062 |
rs16940203 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | GGA2 | GRCh38.p7 | 16:23497235 | GCTCTGGAAATGAGG[C/T]GTTGCTTCTCGGGGC | 23062 |
rs17742339 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | GGA2 | GRCh38.p7 | 16:23482752 | TCTTACTGAAGCCTG[A/G]ATCCTGCTGGAAGTC | 23062 |
rs17742393 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | GGA2 | GRCh38.p7 | 16:23488889 | ATCTCTTAGGAGAAT[C/G]CAAGGGACCATGGTG | 23062 |
rs28377904 | snp | C/G | 0.0531684 | 0.154134 | intron-variant | GGA2 | GRCh38.p7 | 16:23508936 | GATTTCTCCTTGTCC[C/G]CTGTCTGCATTCCAA | 23062 |
rs28504053 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475939 | CATCTCAGGAAAAAA[A/G]AAAGAAAAAAACAAA | 23062 |
rs28523543 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475951 | AAAAAAAGAAAAAAA[C/G]AAAAGCACTTAAAAT | 23062 |
rs28709586 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502450 | CAACAAAAGAGGAAC[A/G]TCTGGGTTCAAACCT | 23062 |
rs34105270 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488748 | AAGACACCGATATGG[G/T]ACCCAGAAACTTCAG | 23062 |
rs34111733 | in-del | -/TTGAGGCTGA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497040 | AGTGGAAAGACTGCG[-/TTGAGGCTGA]GCTGCAGTGAGCCAA | 23062 |
rs34124439 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491297 | AGGTAACAGGGCAAC[A/C]CCTTGTCTCAAAAAA | 23062 |
rs34195789 | in-del | -/T/TT/TTT | 0.5 | 0 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499145 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GATATGGAGTCTCGC | 23062 |
rs34298112 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482051 | GCAGACGGATCACTA[G/T]AGGCCAGAAGTTTGA | 23062 |
rs34320769 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489217 | ACAACAAAACACTGG[-/G]AAAGTGTGCAAATTC | 23062 |
rs34362662 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498182 | TACTCAGTAGGGTGA[-/A]GGCAGGAGAATCGCT | 23062 |
rs34512798 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479101 | CTCTGAACTGCCCAG[-/C]AACACCTGATTCCCT | 23062 |
rs34560583 | in-del | -/AAAG | 0.437965 | 0.164831 | intron-variant | GGA2 | GRCh38.p7 | 16:23475951 | AAAAAAGAAAAAAAC[-/AAAG]AAAAGCACTTAAAAT | 23062 |
rs34615748 | in-del | -/AAAC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470764 | AACAAACAAACAAAC[-/AAAC]AAAAAACAAAAAGCC | 23062 |
rs34685392 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498179 | AGCTACTCAGTAGGG[-/G]TGAGGCAGGAGAATC | 23062 |
rs34718877 | in-del | -/A | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503655 | CACAAGAACTTAAAA[-/A]TGTTGTGTAAAATAC | 23062 |
rs34824899 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481936 | GGAGAAATTTTATCA[G/T]GGCAATCTGAACACT | 23062 |
rs34831881 | in-del | -/A | 0.477937 | 0.102688 | intron-variant | GGA2 | GRCh38.p7 | 16:23491531 | AAAGATTTATTGCGT[-/A]AAAAAAAAAAAAAAA | 23062 |
rs34938422 | in-del | -/C | | | frameshift-variant | GGA2 | GRCh38.p7 | 16:23480690 | GGTCACTCTGTTTCC[-/C]AAAGGTGACCCGGCC | 23062 |
rs34972165 | in-del | -/T/TT | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23473356 | TTTTTTTTTTTTTTT[-/T/TT]AGACAGAGTCTTCTC | 23062 |
rs35084012 | in-del | -/G | | | frameshift-variant | GGA2 | GRCh38.p7 | 16:23480658 | CCTCTGGAGACAGGG[-/G]ATGTCTCCCAATGAG | 23062 |
rs35347154 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491329 | AAAAAAAAAAAAAAA[-/A]CCAAAAGGTTAGTTT | 23062 |
rs35347972 | snp | A/G | 0.0421432 | 0.138908 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23468973 | AGTGAAGCTGCAGCC[A/G]GCATCCAGCTCCAAG | 23062 |
rs35359274 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481980 | ATTATTCTGAAATGT[C/G]CAGAGGCCGGGGATC | 23062 |
rs35419934 | snp | A/G/T | 6.59217e-05 | 0.00574078 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474977 | CTGGGAGGCTGGCCC[A/G/T]TTGGCTCCTTCCCCA | 23062 |
rs35598942 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470214 | CACTACAAACCCCCC[-/C]GGACAGCCAGGCTGG | 23062 |
rs35767669 | snp | G/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502081 | GTCCAAAAAACTTTA[G/T]AATTGGCTCCAGATT | 23062 |
rs35896041 | in-del | -/TTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487000 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGGGTCTTGC | 23062 |
rs35947720 | in-del | -/TT | 0 | 0 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511331 | CTATTTTTTTTTTTT[-/TT]GTATTTTTAGTAGAA | 23062 |
rs36021060 | in-del | -/C | 0.438526 | 0.164189 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510553 | ACCCCAGGCCCCCCC[-/C]TCCACGCGGGACCGG | 23062 |
rs36067397 | in-del | -/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23470847 | TTTTTTTTTTTTTTT[-/T]GGACAGACTTTCGCT | 23062 |
rs36122288 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478843 | GGCAGGTCTGAGACC[-/C]TCCCATTCTCTCTCC | 23062 |
rs36122804 | snp | C/G | 0.343254 | 0.231956 | intron-variant | GGA2 | GRCh38.p7 | 16:23484073 | GCAGGTGGATCACCT[C/G]AGGCCAGGGTTCAAG | 23062 |
rs55823157 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23497767 | CTGCCCCTTCTCCGA[C/T]AGGGATCTCCAGCTA | 23062 |
rs55829210 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499820 | GACCTTCCTCACAGT[A/G]TAGAAACCTGAAAGC | 23062 |
rs56010316 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476962 | AAGCAGCACATTAAA[C/T]TTTTTTTGAGACAGG | 23062 |
rs56057426 | in-del | -/CAAA/CAAACAAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470767 | AAACAAACAAACAAA[-/CAAA/CAAACAAA]AAACAAAAAGCCACA | 23062 |
rs56134479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507884 | AAATGCTTGAGCCCA[A/G]GAGAGGGGTAAGCTG | 23062 |
rs56255431 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498860 | TTTAAAGCAGTGATT[C/T]TCAGCGATTATGTGT | 23062 |
rs56306216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500768 | TGGAGCCTGCCCAGT[C/T]GGATTTAGGAGCCCG | 23062 |
rs57252579 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467478 | ACACCCAGAGCCTGA[C/T]GTCAGGATAGGACTC | 23062 |
rs57255054 | in-del | -/CACACACA | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467427 | ACACACACACACACA[-/CACACACA]GAGCATCTGCAGAAT | 23062 |
rs57258063 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495097 | AAAAAAAAAAGAAAA[C/G]AAAAGAAAACAAAAC | 23062 |
rs57500272 | in-del | -/GTGT/GTGTGTGT | 0 | 0 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511050 | TGTGTGTGTGTGTGT[-/GTGT/GTGTGTGT]TAGAGACTGGGTTTC | 23062 |
rs57694752 | in-del | -/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511515 | ACTTTTTTTTTTTTT[-/T]CAGATGGAGTCTCGC | 23062 |
rs57841058 | in-del | -/GAAAA | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23495102 | AAAAAGAAAAGAAAA[-/GAAAA]CAAAACAAAAACAAA | 23062 |
rs58060392 | in-del | -/TTT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511330 | GCTATTTTTTTTTTT[-/TTT]GTATTTTTAGTAGAA | 23062 |
rs58137464 | snp | C/G | 0.180064 | 0.240019 | intron-variant | GGA2 | GRCh38.p7 | 16:23492885 | ATGCAACTCAGGGGA[C/G]TGTCAGAACTGAAAT | 23062 |
rs58827446 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503709 | ACTGCATACTGAATA[A/G]AAGGAAAACGGATTT | 23062 |
rs58978917 | snp | A/C/G | 1.64874e-05 | 0.00287113 | intron-variant | GGA2 | GRCh38.p7 | 16:23491628 | ATGAAAAAGCAAGAA[A/C/G]ATACAGGCCTAGTCA | 23062 |
rs59197241 | snp | G/T | 0.176861 | 0.239062 | intron-variant | GGA2 | GRCh38.p7 | 16:23492857 | AGCCCTCACTGCGTG[G/T]GGTCCGGGTAGCATG | 23062 |
rs59699849 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | GGA2 | GRCh38.p7 | 16:23472168 | CTGGCATCCAAAGAT[A/G]TTCTTTGTAGCCCTG | 23062 |
rs59718939 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | GGA2 | GRCh38.p7 | 16:23468697 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTCAGGTG | 23062 |
rs59721453 | snp | A/C | 0.031825 | 0.122064 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467256 | CTGATAAAACCTCCA[A/C]CCTGAGGCAGGGACA | 23062 |
rs59785925 | in-del | -/TTGAGGCTGA | 0.285519 | 0.247464 | intron-variant | GGA2 | GRCh38.p7 | 16:23497039 | AAGTGGAAAGACTGC[-/TTGAGGCTGA]GGCTGCAGTGAGCCA | 23062 |
rs60519528 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23497913 | CCAAGGCAGGAGGAC[C/T]GCTTGAGCCTAGGAG | 23062 |
rs60756560 | snp | C/T | 0.178785 | 0.239642 | intron-variant | GGA2 | GRCh38.p7 | 16:23506659 | GCCCAAGATGTCACT[C/T]GTGCAAAGGTTGAGA | 23062 |
rs60801698 | snp | A/T | 0.24019 | 0.249807 | intron-variant | GGA2 | GRCh38.p7 | 16:23492752 | ATAGGAACCCCTGAA[A/T]CTGCAGCTGGGGATG | 23062 |
rs60806846 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | GGA2 | GRCh38.p7 | 16:23507460 | TGGTGAAACCCTATC[A/G]CTACTAAAAATACAA | 23062 |
rs61552681 | in-del | -/CACACACACACACACACACACACACA | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467434 | ACACACACACACACA[-/CACACACACACACACACACACACACA]GAGCATCTGCAGAAT | 23062 |
rs62029426 | snp | A/C | 0.0123036 | 0.0774623 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465962 | CAAAAAAAAGCCACA[A/C]AGAATACAAGCAAGA | 23062 |
rs62029427 | snp | G/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23474376 | CTTTTTTTTTTTTTG[G/T]AGACGGAGTCTCACT | 23062 |
rs62029428 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474864 | TCTAATAGATTCCCA[A/G]GGAAAAAAAAAAAAA | 23062 |
rs62029453 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23505321 | GCTAGAATTCTAGAG[C/T]CCAAGAGGACTGAGT | 23062 |
rs62029454 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507508 | TGGCTAATGCCTGTA[A/G]TCCCAGCTACTTGGG | 23062 |
rs62029455 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507511 | CTAATGCCTGTAATC[C/T]CAGCTACTTGGGAGG | 23062 |
rs62029457 | snp | A/C/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511455 | TGAGCCACCACGCCC[A/C/G]GCCTATGTGCTTGCA | 23062 |
rs66569010 | snp | C/T | 0.437824 | 0.164991 | intron-variant | GGA2 | GRCh38.p7 | 16:23475631 | CTTAGAGGCTGGGCA[C/T]GGTGGCTCACGCCTG | 23062 |
rs67594368 | snp | A/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23495092 | GGAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAC | 23062 |
rs67653354 | snp | A/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23473356 | TTTTTTTTTTTTTTT[A/T]AGACAGAGTCTTCTC | 23062 |
rs71154215 | in-del | -/A | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23491329 | AAAAAAAAAAAAAAA[-/A]CCAAAAGGTTAGTTT | 23062 |
rs71378625 | in-del | CTATCAGCTGTCTA/GTAT | 0.5 | 0 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511972 | AATTATTTTGCATTG[CTATCAGCTGTCTA/GTAT]CAACTTAACAGAGTT | 23062 |
rs71379682 | in-del | -/A | 0.391583 | 0.206044 | intron-variant | GGA2 | GRCh38.p7 | 16:23473031 | CGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 23062 |
rs71379818 | snp | A/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23491835 | AGAATTCTAGAGCTG[A/G]AAGGGACTTGGGAGA | 23062 |
rs71379819 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | GGA2 | GRCh38.p7 | 16:23507073 | AAATTCCCTCTCGCT[A/G]TTCTCTCCCCCTCCT | 23062 |
rs71717530 | in-del | -/AG | 0.183886 | 0.241099 | intron-variant | GGA2 | GRCh38.p7 | 16:23486225 | AACAAGGGATGGGAA[-/AG]AGTCACTATTGAGAG | 23062 |
rs71722726 | in-del | -/CA | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467433 | ACACACACACACACA[-/CA]GAGCATCTGCAGAAT | 23062 |
rs71876061 | in-del | -/CTTCTC | 0.178785 | 0.239642 | intron-variant | GGA2 | GRCh38.p7 | 16:23468117 | TTCTTTTCTTTTTCT[-/CTTCTC]CTTCCTTCCTTTCCT | 23062 |
rs72532662 | in-del | -/CA | 0 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466678 | ATGTCTATCTGTACC[-/CA]AGTTTCCCATCTTAG | 23062 |
rs72774396 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23483123 | CTTCAGAAGGCCTCC[C/T]AATGGTCCTGACTTA | 23062 |
rs72776106 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | GGA2 | GRCh38.p7 | 16:23509437 | AACGAACGCCCTCCT[C/G]CTCCTCGCCAATCCC | 23062 |
rs74012179 | snp | C/G | 0.00247122 | 0.0350643 | intron-variant | GGA2 | GRCh38.p7 | 16:23478752 | TGAGGAAGAGGCTTT[C/G]GACCTCCAAGGCCAT | 23062 |
rs74012181 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | GGA2 | GRCh38.p7 | 16:23492547 | CTCAGTTGAACCTAC[A/G]TTGGGAGGATGGCAA | 23062 |
rs74012183 | snp | A/G | 0.00375814 | 0.043185 | intron-variant | GGA2 | GRCh38.p7 | 16:23493508 | AAGCCAGTGGTCCCA[A/G]GCTCCCCTCCAGGCT | 23062 |
rs74012184 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23498740 | CTGTAATATGTAGAC[A/G]TGTCTTGTCCTACCT | 23062 |
rs74012185 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499022 | GAGAACAGGGGGAGG[C/T]AGGGAGAGAACAGGA | 23062 |
rs74014924 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501517 | CCGTGACCTGTATTT[C/T]CTATTTAGTTTTCCT | 23062 |
rs74014925 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | GGA2 | GRCh38.p7 | 16:23505911 | GCCTACCCCTACTCT[A/G]GGACTTTCTTTACTT | 23062 |
rs74486558 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | GGA2 | GRCh38.p7 | 16:23475970 | AGCACTTAAAATGTC[C/T]ACACATAATAAGAAC | 23062 |
rs74786534 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23492829 | TGAAACACAGGAAGC[C/T]TAAGCAGCACTGAGC | 23062 |
rs75042543 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | GGA2 | GRCh38.p7 | 16:23471134 | GCGTGAGCCACTGCA[A/C]CCGGCCAATGCATTC | 23062 |
rs75057100 | snp | A/C | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23509743 | AGGAAAAAAAAAACA[A/C]ACATATATATATATA | 23062 |
rs75094924 | snp | A/G | 0.179425 | 0.239831 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466508 | TTTCCTTTACTTCTC[A/G]ACAGAAGACAGTTCC | 23062 |
rs75263022 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23495155 | TGATTCTGATTCTTC[A/G]GGTCCTATCCAGATG | 23062 |
rs75706480 | snp | C/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23485723 | GTGAATGGATCTCGA[C/G]TGAGATCCAGAAACC | 23062 |
rs75719789 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | GGA2 | GRCh38.p7 | 16:23487528 | TTATGACACAACAGA[C/T]CCTGGTGATCTTGTT | 23062 |
rs75789233 | snp | G/T | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23474374 | AACTTTTTTTTTTTT[G/T]GGAGACGGAGTCTCA | 23062 |
rs75797272 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | GGA2 | GRCh38.p7 | 16:23471981 | AAGAGACTGAAAATA[C/T]CAGTGGGGTATGGTG | 23062 |
rs76064767 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506899 | GAGGCCAGGTCCCCC[C/T]TTTTGCTCTGGCTCT | 23062 |
rs76108586 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23472893 | CAAAAAAGTAGCTGG[A/G]CGTGGTTGTGGGCAC | 23062 |
rs76136326 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512045 | AGGTTGTGCTGTCTA[A/G]ACAACACATAATTTT | 23062 |
rs76582657 | snp | C/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23498265 | AGCCTGGGTGACAAG[C/G]TGAGACTCTGTCTCC | 23062 |
rs77075829 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | GGA2 | GRCh38.p7 | 16:23484961 | AGGCATCATTCATAA[C/T]AGCCAAAAAGTAGGA | 23062 |
rs77126453 | in-del | -/C | | | frameshift-variant | GGA2 | GRCh38.p7 | 16:23480667 | GACAGGGATGTCTCC[-/C]AATGAGCTGGTCACT | 23062 |
rs77343820 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | GGA2 | GRCh38.p7 | 16:23506458 | ACTCAGGAACTCAGC[A/G]GGGAGATGGGTAGGA | 23062 |
rs77378340 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499069 | GGCATGGCCCAAGCT[C/T]CCCTCACAGAATCCA | 23062 |
rs77452128 | snp | C/T | 0.0396539 | 0.135109 | intron-variant | GGA2 | GRCh38.p7 | 16:23478804 | GAGCACCTCTCTGCT[C/T]GCCAGGCAGTGCTGC | 23062 |
rs77455622 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | GGA2 | GRCh38.p7 | 16:23489073 | AAAATGCTGAGTGTA[C/T]GTGACAGGGAACAAC | 23062 |
rs77463366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23506524 | CAGTATCTGGTGACA[C/T]TTTTGGCTGTTATGA | 23062 |
rs77595603 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | GGA2 | GRCh38.p7 | 16:23484379 | GCTGAGATCACGCAA[C/T]TGCACTCCAGCCTGG | 23062 |
rs78289271 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | GGA2 | GRCh38.p7 | 16:23469924 | CTTGACACTCGACAG[G/T]TAAGTCCCAGAAAAG | 23062 |
rs78479883 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504245 | AGTCATAGGCTGGCC[C/T]AGCTCCACAGCCTGG | 23062 |
rs78569702 | snp | A/C | 0 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464552 | GGACAGAGGCATTGT[A/C]CCAAAAAAAAAAAAG | 23062 |
rs78606198 | snp | G/T | 0.0130921 | 0.0798413 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463576 | TTTCAGCTGATTTTA[G/T]AAAGCTCAGAAAAAA | 23062 |
rs78684194 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | GGA2 | GRCh38.p7 | 16:23497613 | CCCCCGCAAAGCTCT[C/G]TCCCATGTTCCGTAT | 23062 |
rs78723493 | snp | A/T | 0.114738 | 0.210248 | intron-variant | GGA2 | GRCh38.p7 | 16:23471919 | ATCTCTAAAAAAATT[A/T]AAAAAAAAATTAAAA | 23062 |
rs78926502 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23495384 | GTGTTTTTTTTCCCC[C/T]ACATGAATTTGCTAA | 23062 |
rs79170034 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | GGA2 | GRCh38.p7 | 16:23468097 | AACCAAACCAGAGAC[C/T]GACTTTCTTTTCTTT | 23062 |
rs79515799 | snp | C/T | 0.000625782 | 0.0176777 | missense | GGA2 | GRCh38.p7 | 16:23491719 | CTCGAATCTTGATGT[C/T]TTCCGGAAACCAGAC | 23062 |
rs79530662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504374 | TGAAGGCAAAAAGCA[A/G]GCCTGTCTCATTCAC | 23062 |
rs79827089 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504083 | TGAAACTCCGTCTCA[A/C]AAAAAAAAAAAAAAG | 23062 |
rs79925671 | snp | A/C | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23497120 | AAAAACAAAAAAAAA[A/C]AACAACCACCCTTCC | 23062 |
rs80319662 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23507424 | CTTGAGGTCAGGAGT[C/T]TGAGACCAGCCTGAC | 23062 |
rs111228093 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467435 | ACACACACACACACA[C/G]AGCATCTGCAGAATA | 23062 |
rs111229895 | in-del | -/A | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23478225 | AAAAGAAAAAAAGAC[-/A]AAAAAAAAAAAAAAG | 23062 |
rs111241989 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | GGA2 | GRCh38.p7 | 16:23471932 | TTTAAAAAAAAATTA[A/G]AACATAGTTTAACAA | 23062 |
rs111294282 | snp | A/C/G | 1.65864e-05 | 0.00287974 | splice-donor-variant | GGA2 | GRCh38.p7 | 16:23482922 | AGGAAAGAAAACTTA[A/C/G]CGAGTGCATCATCGT | 23062 |
rs111398739 | snp | A/C | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23483228 | ATAAAATAATCTGAC[A/C]GGGCAGGGTGGCTCA | 23062 |
rs111482122 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23497436 | AGTTGAATTTTTCCT[C/G]ACTGCAGTCACATTT | 23062 |
rs111554460 | snp | A/C | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23484303 | CATTCCTGTAATCCC[A/C]GCTCCTCGGGAGGCT | 23062 |
rs111556252 | snp | A/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23495845 | CCCCTCCCCATACAC[A/G]TGGTGGCCAAGAGCT | 23062 |
rs111559951 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464139 | CAATTTACACTATTT[A/G]TACTAGGTAATATTC | 23062 |
rs111731731 | snp | A/C/G | 1.65894e-05 | 0.00288 | splice-donor-variant | GGA2 | GRCh38.p7 | 16:23482921 | AAGGAAAGAAAACTT[A/C/G]CCGAGTGCATCATCG | 23062 |
rs111787525 | snp | A/G | 0.029116 | 0.117091 | intron-variant | GGA2 | GRCh38.p7 | 16:23492843 | CCTAAGCAGCACTGA[A/G]CCCTCACTGCGTGGG | 23062 |
rs111792605 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23488769 | GAAACTTCAGTCAGA[A/T]TCCAGTATAAAGTCT | 23062 |
rs111796012 | snp | A/G | 0.5 | 0 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470061 | TGCTCATCATGGTCA[A/G]GAGCAGCACCTGTAC | 23062 |
rs111881819 | snp | A/G | 0.029116 | 0.117091 | intron-variant | GGA2 | GRCh38.p7 | 16:23477702 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 23062 |
rs111918232 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | GGA2 | GRCh38.p7 | 16:23475785 | AAATAAAAAATTAGC[C/T]AGGTGGTGGTGGCAC | 23062 |
rs111958098 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23510101 | GGGTGGGCGGAGGGG[A/G]AGGGGCAGAGCTCAG | 23062 |
rs111964214 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | GGA2 | GRCh38.p7 | 16:23472128 | AAGGTATAAAGAAAG[G/T]CATCCAAAGATGTTC | 23062 |
rs111965199 | snp | G/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23484331 | GCTGAGGCAGGAGAA[G/T]CGCTCGAACCCGGGA | 23062 |
rs112018610 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467439 | ACACACACACAGAGC[A/G]TCTGCAGAATAAGTC | 23062 |
rs112020595 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23480927 | CGGACCCTATCAGGC[C/T]TAGTCAGTTAACCTG | 23062 |
rs112123490 | in-del | -/A | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23471568 | ACTGGTTAATCAGCT[-/A]AAAAAAAAAACCTTA | 23062 |
rs112143857 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | GGA2 | GRCh38.p7 | 16:23494635 | AACCCCCAGCCCCCA[A/G]ACTCCAAGCTGCCAG | 23062 |
rs112167961 | snp | A/C | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23498092 | GGAGGCCAGCCTGGG[A/C]AACACGGTGAAATCC | 23062 |
rs112194524 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23483943 | TGAGCCACTGCGCCC[A/G]GCTGGGCTGTGGTTT | 23062 |
rs112294873 | in-del | -/CAGCTGTCTA | 0.285257 | 0.247501 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511975 | ATTTTGCATTGGTAT[-/CAGCTGTCTA]CAACTTAACAGAGTT | 23062 |
rs112454700 | snp | C/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23496450 | AGCGGAGACAGAAGA[C/G]AGGCCACCTGGAAGT | 23062 |
rs112455000 | snp | A/C | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23467925 | AGAGACCAGCTAAGG[A/C]AGACAGACCTTGTCC | 23062 |
rs112525487 | in-del | -/CAAA/CAAACAAA | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23470747 | AGCGAGACTCTGTCT[-/CAAA/CAAACAAA]CAAACAAACAAACAA | 23062 |
rs112568758 | snp | G/T | 0.0295035 | 0.117819 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510469 | TCAGCCGCTGTAGCG[G/T]CCTGGCGCTCTCCTC | 23062 |
rs112599925 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465849 | GAGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 23062 |
rs112695848 | snp | C/T | 0.0295035 | 0.117819 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511431 | CCCAAAGTGCTGGGA[C/T]TACAGGGGTGAGCCA | 23062 |
rs112701553 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | GGA2 | GRCh38.p7 | 16:23475611 | GAGACGATGTATGAA[A/C]AGCACTTAGAGGCTG | 23062 |
rs112730560 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23493930 | CACTCAAACATATAC[A/G]AAGACCTAAACTAGC | 23062 |
rs112767915 | snp | A/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23484237 | ACATAGAGAAACCCT[A/G]TCTCTACTTAAAAAA | 23062 |
rs112775952 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23493075 | GGGATCTCTCACTGT[C/T]TCTATCAGGAACCTG | 23062 |
rs112777996 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | GGA2 | GRCh38.p7 | 16:23489239 | TGCAAATTCACAATA[C/T]TTTTGTTGTTTTTGA | 23062 |
rs112778294 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | GGA2 | GRCh38.p7 | 16:23507640 | CTCTCTCTCTCTCTC[A/T]CACACACAAATTAGC | 23062 |
rs112893762 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | GGA2 | GRCh38.p7 | 16:23480024 | CAAGAACCTTCCACT[A/C]AGCTGAGTGTCCTGA | 23062 |
rs112946923 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23481478 | GAGGGCCTATTTTCA[C/T]GCAAGGAAAAAAGGC | 23062 |
rs112980836 | in-del | -/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23481888 | TCTGATTTAGAACAA[-/T]TTTTTTTTTTTAAGT | 23062 |
rs113111137 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | GGA2 | GRCh38.p7 | 16:23475632 | TTAGAGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 23062 |
rs113197951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23509482 | GTGACTGCCGGCTTG[C/T]ACCCACTAAAAAATG | 23062 |
rs113270943 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23479376 | TACTCACACCCATCC[C/T]GATTCCCTCAGCAGC | 23062 |
rs113280427 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465464 | TACCACTGGGAGTCT[A/G]TCTCCTCAAAAGCAA | 23062 |
rs113319424 | snp | C/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23479373 | CCCTACTCACACCCA[C/T]CCCGATTCCCTCAGC | 23062 |
rs113348656 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | GGA2 | GRCh38.p7 | 16:23488537 | ATACTCCGATTCAAG[C/T]ATCAAAGGGCATTTA | 23062 |
rs113363045 | snp | A/G | 0.0577344 | 0.159793 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500886 | GAGAAAATATCAAAT[A/G]AGTGTGCAAGAAAAG | 23062 |
rs113417385 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23509790 | CGTGTGTGTGTGTTT[-/A]AAAAAAAAAGTCTGG | 23062 |
rs113419569 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | GGA2 | GRCh38.p7 | 16:23486433 | CCTGGACTTTGTCCA[C/T]ACCAATACCTGTTGC | 23062 |
rs113544600 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | GGA2 | GRCh38.p7 | 16:23494935 | AAAAAAATACAAAAA[A/G]TTAGCCAGGCATGGA | 23062 |
rs113556190 | snp | A/T | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23469806 | TTGTTTAAGAACCTA[A/T]TTGGATTCACTCATA | 23062 |
rs113563727 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | GGA2 | GRCh38.p7 | 16:23498546 | AAGCCTGGGCAACAT[A/G]GTGAGGCCCCATCTC | 23062 |
rs113612998 | snp | A/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23497884 | CATGCCTATGATCCC[A/G]GCACTCTGGGAAGCC | 23062 |
rs113615058 | snp | C/T | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23476247 | CTGAAAAAAAGAAGA[C/T]TGCAAGAAATGACCT | 23062 |
rs113814429 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464554 | CAGAGGCATTGTCCC[-/A]AAAAAAAAAAAAGCC | 23062 |
rs113890756 | snp | C/G | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23493570 | CAAGGCTAACCCTGC[C/G]TCAAGCCTATGAGGA | 23062 |
rs114277071 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23494074 | ATAAAACCTTCCTTT[C/T]CTTCTCCCACAGTAG | 23062 |
rs114861239 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501930 | CTTGAACAACTCTTG[A/G]GGAGAAGGAGTGTCA | 23062 |
rs115026600 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | GGA2 | GRCh38.p7 | 16:23509781 | ACACACACACGTGTG[G/T]GTGTGTTTAAAAAAA | 23062 |
rs115041041 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512239 | TGTAAAGAGCATCAG[C/T]TTATATAGTATTTTC | 23062 |
rs115308394 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463669 | AACATCTTGGTGCAT[C/T]GCTTGGCTTTAAAAC | 23062 |
rs115432813 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466119 | CTCCACCAATTAGTA[C/T]TGGCAGATTTCCACT | 23062 |
rs115577456 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23477780 | AAAAACACATGCCTT[C/T]TGCCTTCCGCCATGA | 23062 |
rs115783705 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512454 | ATTCTTCTTAGACCA[C/T]AGGTACGTATGCCAT | 23062 |
rs115804250 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23504840 | TGTATTTCCTCACTA[A/C]AAGCAGTGTTTGTAT | 23062 |
rs116219854 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486984 | GTTTTCTTTTCTGTT[G/T]TTTTTTTTTTTTTTT | 23062 |
rs116538049 | snp | C/G | 0.00478085 | 0.0486577 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463313 | TGAGCTCAGGGAAGA[C/G]AGCGGGGTTATGTTT | 23062 |
rs116586682 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | GGA2 | GRCh38.p7 | 16:23492793 | GCAGCTTGAGGACAC[A/G]TGAGACTCACGGCTG | 23062 |
rs116760637 | snp | A/C/G | 0.00298309 | 0.0385087 | intron-variant | GGA2 | GRCh38.p7 | 16:23478805 | AGCACCTCTCTGCTC[A/C/G]CCAGGCAGTGCTGCC | 23062 |
rs116984818 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | GGA2 | GRCh38.p7 | 16:23494806 | ATCTGGATGGGCCAG[A/G]CACAGTGGCTCACGC | 23062 |
rs116992345 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23482350 | GAGAGGTACAGATGA[A/C]GTAAGATTAAAAAAA | 23062 |
rs117001927 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23507044 | CTCTCCTTCTAATAA[A/T]CTCCTTTACTCCTAA | 23062 |
rs117216889 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | GGA2 | GRCh38.p7 | 16:23505551 | AATGCACAGGCGCTG[C/T]CGTTTGTACTTTTAA | 23062 |
rs117275016 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | GGA2 | GRCh38.p7 | 16:23492887 | GCAACTCAGGGGAGT[A/G]TCAGAACTGAAATGA | 23062 |
rs117323704 | snp | C/T | 0.00264205 | 0.0362497 | missense | GGA2 | GRCh38.p7 | 16:23482941 | GTGCATCATCGTCAT[C/T]AGTGGTGTCACTCGC | 23062 |
rs117335381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503411 | TTAGTTGTAATAATG[A/G]TATTTTCTTTTTTAT | 23062 |
rs117714554 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | GGA2 | GRCh38.p7 | 16:23488448 | TTATCCATGAAGAAC[A/G]CACCCAAACCTTCTG | 23062 |
rs118057012 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | GGA2 | GRCh38.p7 | 16:23473421 | AGCTCACTGCAACTT[C/T]TGCCATCTGGGTTCA | 23062 |
rs118071508 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503804 | ACCTAATATGGGGCC[A/G]GGTGTAGTGGCTCAT | 23062 |
rs118145160 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23486266 | AGGGGCATCACCAGG[A/G]TGTTAAGTGCATGGG | 23062 |
rs137997253 | snp | C/T | 8.6175e-05 | 0.00656354 | intron-variant | GGA2 | GRCh38.p7 | 16:23491852 | AGGGACTTGGGAGAC[C/T]GACACTTTAACTAAA | 23062 |
rs138034871 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant | GGA2 | GRCh38.p7 | 16:23488725 | CTAAAAATGCAATTT[A/G]CAAAGTTAAGACACC | 23062 |
rs138101012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493267 | GCAGGTTTTGTCCAT[A/G]CGTGGGCCTGCCTCT | 23062 |
rs138375589 | snp | C/G | 0.184521 | 0.241273 | intron-variant | GGA2 | GRCh38.p7 | 16:23472350 | AGGCGCCCACCACCA[C/G]GCCTGGCTAATTTTT | 23062 |
rs138397318 | snp | A/G/T | 0.000131836 | 0.008118 | missense, synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494308 | CCAAACTCACCGTTA[A/G/T]GGCATAAAGAGCTTC | 23062 |
rs138408688 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466115 | CCATCTCCACCAATT[A/G]GTATTGGCAGATTTC | 23062 |
rs138430424 | snp | A/C | 0.00227899 | 0.0336794 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23482942 | TGCATCATCGTCATC[A/C]GTGGTGTCACTCGCC | 23062 |
rs138463237 | snp | C/T | 0.000298875 | 0.0122208 | intron-variant | GGA2 | GRCh38.p7 | 16:23495811 | AAGTTAGAGAGTACA[C/T]AATAGGAAGAAATTT | 23062 |
rs138528703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23508916 | GAAACCCGCGATCTA[A/G]CCTAGATTTCTCCTT | 23062 |
rs138560859 | snp | A/T | 0.000132046 | 0.00812438 | missense | GGA2 | GRCh38.p7 | 16:23480651 | CAAACATACCTCTGG[A/T]GACAGGGATGTCTCC | 23062 |
rs138633096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23488986 | TATGCTGTAAAAGCA[C/T]GGATCAGTTTATCCA | 23062 |
rs138752639 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465878 | CCTGGTAGGCAGAGA[C/T]TGCAGTGAGCTGAGA | 23062 |
rs138770670 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503718 | TGAATAAAAGGAAAA[A/C]GGATTTTCCTATGGG | 23062 |
rs138789470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23497539 | ACTCCATTCTAAGTG[A/G]AGAGAGAACACAAGG | 23062 |
rs138912386 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | GGA2 | GRCh38.p7 | 16:23472664 | AGTAAGCTGAGATGG[C/T]GCCACTGCACTCCAG | 23062 |
rs138923765 | snp | A/G | 0.000148698 | 0.00862129 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494378 | GGGCGCATGTGTGGG[A/G]CTACAGGGAAACAAA | 23062 |
rs138985550 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | GGA2 | GRCh38.p7 | 16:23509760 | CATATATATATATAC[A/G]CACACACACACACAC | 23062 |
rs139018883 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | GGA2 | GRCh38.p7 | 16:23481642 | GCCAGGTGTGGTGGT[A/G]CGCAACTGTAGTCCC | 23062 |
rs139134646 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491304 | AGGGCAACACCTTGT[C/T]TCAAAAAAAAAAAAA | 23062 |
rs139166446 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23508291 | GGCTGGTCTTAAACT[C/T]CTGGCCTCAAAGGAT | 23062 |
rs139178700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23474229 | TTAAACATTCCCTTC[C/T]TGAATCCCAACCCAA | 23062 |
rs139215193 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | GGA2 | GRCh38.p7 | 16:23468339 | CACGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 23062 |
rs139277715 | in-del | -/AC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467387 | CCACCCTCTCCCCGA[-/AC]ACACACACACACACA | 23062 |
rs139305678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484797 | CCACTTTGGAAAACA[A/G]CTTGGCAGTTCCTCA | 23062 |
rs139441213 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | GGA2 | GRCh38.p7 | 16:23468013 | CTATGACAATCCATC[C/T]GATCTTCCTTCAGTG | 23062 |
rs139549457 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | GGA2 | GRCh38.p7 | 16:23474474 | GCAGTTCTCCTGCCT[C/G]AGCCTCCCAAGTAGC | 23062 |
rs139622093 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23483601 | CAACAGCATGGCTGC[C/G]TCGAACCTGGCACAG | 23062 |
rs139733534 | snp | A/G | 1.65776e-05 | 0.00287898 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23468961 | GAATGCAGGAAGCTT[A/G]GAGCTGGATGCCGGC | 23062 |
rs139764169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479619 | CTCAGCAGCAAGCAC[A/G]TGCTCCCAGAGGGAA | 23062 |
rs139803845 | snp | C/T | 0.00016475 | 0.00907457 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486111 | TCGCACTTCCTCCAC[C/T]GCACTGACCCTCTTG | 23062 |
rs139811732 | snp | C/G | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23470053 | GGGAGCCGTGCTCAT[C/G]ATGGTCAAGAGCAGC | 23062 |
rs139883655 | snp | A/G | 0.0267878 | 0.112589 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510506 | CTGCGCGGCAGGAGC[A/G]GTGGACACGTGACGG | 23062 |
rs139906782 | in-del | -/AAAGA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495099 | AAAAAAAAGAAAAGA[-/AAAGA]AAACAAAACAAAAAC | 23062 |
rs139929528 | snp | A/C | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23486041 | CCTGGTCGGGCGGGG[A/C]CTGCCCTGGCCTGCG | 23062 |
rs139999427 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463987 | AACAAACAAACCCAC[A/T]TTTATACTCTTGACG | 23062 |
rs140040489 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463276 | AGCACTTTCAACACA[G/T]AAGTGCTTGATTTGT | 23062 |
rs140054201 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | GGA2 | GRCh38.p7 | 16:23494200 | AACCTCTCAGGGGAC[C/T]TCCCTTCTCCAGTGA | 23062 |
rs140094366 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | GGA2 | GRCh38.p7 | 16:23489884 | ACAGGGGAGAAAAAA[C/T]AAAAACAAACCCTAG | 23062 |
rs140129619 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23510081 | TGTGCTGCTGCTAAG[-/T]TGGGGGGTGGGCGGA | 23062 |
rs140210356 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | GGA2 | GRCh38.p7 | 16:23504913 | ACAGCTGAGACCTCC[A/G]GCTGTGAGTGAAATG | 23062 |
rs140233096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501787 | GTTTAGGATTTTCAT[C/T]GAGAGGAAACATCTT | 23062 |
rs140250128 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500522 | AATGCCAGCCCCAAG[A/C]GGGGCAGTGTGCGGG | 23062 |
rs140282248 | snp | C/T | 3.30164e-05 | 0.00406289 | missense | GGA2 | GRCh38.p7 | 16:23493443 | CCCCACAGTGGTTCA[C/T]GCACATCTCCAGCAC | 23062 |
rs140317472 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464436 | TTGATCCCATAAAGT[C/T]AGGCATCAGGAAGCC | 23062 |
rs140434372 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | GGA2 | GRCh38.p7 | 16:23507560 | TTGAACCTGGGAGGC[A/G]GACGTTGCAGTGAGC | 23062 |
rs140536449 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477034 | ATGGCTCACTGCAGC[A/C]TCGACTTTCCGGGCT | 23062 |
rs140597795 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23490224 | TAACACTAGAGGAAT[C/T]TGAAGTCTGATATAG | 23062 |
rs140664660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23480284 | TCCAAGCCAGGGACC[A/G]CATTTCAACCAGTGC | 23062 |
rs140675835 | snp | G/T | 4.99405e-05 | 0.00499677 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23478886 | GGGCATCCTTACCAT[G/T]CCTGTAACAGGAGCA | 23062 |
rs140879923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504425 | AGAAGAGTTGCTGGC[A/G]GGTATCTACTGAATG | 23062 |
rs140903086 | snp | A/C | 0.00636936 | 0.0560724 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465083 | GCACACACATCATGA[A/C]TTTGCTTCTCCCCAG | 23062 |
rs140921940 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512456 | TCTTCTTAGACCATA[C/G]GTACGTATGCCATAC | 23062 |
rs140977846 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507241 | AGAATATAGGTTCTA[A/G]CCGTTCCTGAAAAAC | 23062 |
rs141018418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23498947 | AAGGTTGACACCTCA[A/G]AAGAATTCTGACTTC | 23062 |
rs141116445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23494737 | CTAGAGCAGAAAGTG[C/T]GATCAAACTCTGGGT | 23062 |
rs141154774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23488407 | AACCAGGCTGAATCA[A/G]AACAGACTGGCCCTT | 23062 |
rs141249371 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23479263 | CCTCAGCAGCAGGCA[C/T]GTGCTTCCTGAGGAG | 23062 |
rs141326611 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | GGA2 | GRCh38.p7 | 16:23486271 | CATCACCAGGATGTT[A/C]AGTGCATGGGAGAAC | 23062 |
rs141410854 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23483424 | GGAAAGACAGTAGTT[-/C]CATTTCTACTAATCT | 23062 |
rs141419085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481525 | CGCCTGTAATCCCAG[C/G]ACTTTGGGAAGCCAA | 23062 |
rs141472639 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GGA2 | GRCh38.p7 | 16:23475313 | TCCTGACTCAGCCTC[C/T]CGAGTAGCTGGGATT | 23062 |
rs141484348 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463153 | ATTGAGGCGAGAGGG[C/T]TGCCAGGGAAAAGTC | 23062 |
rs141495211 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23473793 | CCAGATGTTAACATC[A/G]TAACTACAATACAGT | 23062 |
rs141601207 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467280 | AGGGACAGTGTCGCT[C/T]GCTGACATGCAGAAA | 23062 |
rs141609601 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23482355 | GTACAGATGAAGTAA[C/G]ATTAAAAAAATCAGC | 23062 |
rs141916682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504295 | TGCGGTGAGGTCTTC[A/G]GTTCCTTGACAAAGT | 23062 |
rs141920722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503918 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAATT | 23062 |
rs141929678 | snp | C/T | 4.94727e-05 | 0.00497332 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494333 | AGCTTCCTTCTCTTG[C/T]GGAGACTGGATCTTG | 23062 |
rs142028444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509339 | TCTCTTGTCCCCAGC[G/T]TTTGCACACGCAGTT | 23062 |
rs142056383 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23495393 | TTCCCCCACATGAAT[G/T]TGCTAATTTTAGAAA | 23062 |
rs142094545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492225 | TTCACTAATGACTTA[C/G]AGTGAGTGCCTAGAG | 23062 |
rs142107518 | snp | C/G/T | 0.000136756 | 0.00826813 | missense | GGA2 | GRCh38.p7 | 16:23467668 | CTGTCCACCTTGGTT[C/G/T]AATGTCAGCTTGTAC | 23062 |
rs142146460 | snp | C/T | 0.000461422 | 0.0151822 | missense | GGA2 | GRCh38.p7 | 16:23480701 | TTTCCAAAGGTGACC[C/T]GGCCCTCCATCACCT | 23062 |
rs142242939 | snp | A/C | 0.00475464 | 0.0485254 | intron-variant | GGA2 | GRCh38.p7 | 16:23470196 | CAAGCAGAAGGTTTA[A/C]CACCACTACAAACCC | 23062 |
rs142255554 | snp | A/C/T | 9.99457e-05 | 0.00706852 | missense | GGA2 | GRCh38.p7 | 16:23482991 | CGCAGCTTTTCACAC[A/C/T]TCTCATACACGACCT | 23062 |
rs142422322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476519 | GTCCAAAAAAGGGAA[A/C]TGATCAAATACATCC | 23062 |
rs142462535 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23472382 | TTGTAGTTTTTAGTA[C/G]AGACAGGGTTTCACC | 23062 |
rs142529148 | in-del | -/GTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511017 | GACTGGGTTTCACCG[-/GTGT]TGTGTGTGTGTGTGT | 23062 |
rs142540707 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23506688 | GAAACCCAGCTCTCC[A/G]TCCGGGTGGGCCCAC | 23062 |
rs142732416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493268 | CAGGTTTTGTCCATG[C/T]GTGGGCCTGCCTCTG | 23062 |
rs142803077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489243 | AATTCACAATATTTT[G/T]GTTGTTTTTGAGACA | 23062 |
rs142996376 | in-del | -/ACAA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470755 | TCTGTCTCAAACAAA[-/ACAA]CAAACAAACAAAAAA | 23062 |
rs143003037 | snp | A/C/G | 0.000790847 | 0.0198708 | missense | GGA2 | GRCh38.p7 | 16:23493398 | GTTCGTTCAGGAAAC[A/C/G]AAATTTGGCCACCTC | 23062 |
rs143169737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468201 | TATCTATCTATTTGA[C/T]AGAGTCTCGCTCTGT | 23062 |
rs143177094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23508476 | ATAACTGGTTGGTTA[A/C]CAAATTCAAAGTTCT | 23062 |
rs143217445 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504496 | TGGACATACTGATAA[C/T]ACGGAGAGATGGCTA | 23062 |
rs143266058 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | GGA2 | GRCh38.p7 | 16:23507691 | CGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 23062 |
rs143268241 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | GGA2 | GRCh38.p7 | 16:23476695 | GTACCACTACATGTA[C/T]ACAAAAAAAGCAAAA | 23062 |
rs143311564 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464204 | ACTATCTTCATGACC[G/T]GTTTGTGTTCAGAGT | 23062 |
rs143352877 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510731 | ATTTTTTAAGAGACG[A/G]GGTCTTGCTCTGTCA | 23062 |
rs143393197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23507396 | ACTTCGGGAGGCCAA[A/G]ACTGGCAGATAACTT | 23062 |
rs143414695 | in-del | -/TTGAGGCTGA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497030 | AGGAAGCTGAAGTGG[-/TTGAGGCTGA]AAAGACTGCGGCTGC | 23062 |
rs143560643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496065 | GGCATTTTGGGAGGC[C/T]GAGGTGGGGGGAATC | 23062 |
rs143594050 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23488803 | AACCCCTGGTTCCTA[A/C]TACCATGCTAGCAAA | 23062 |
rs143632395 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23483607 | CATGGCTGCCTCGAA[C/G]CTGGCACAGACAGGC | 23062 |
rs143736915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23493981 | ACCTGCCAACAGCTA[A/G]TGGGCCCTGTGCTAG | 23062 |
rs143753110 | snp | A/C | 0.0035208 | 0.0418091 | intron-variant | GGA2 | GRCh38.p7 | 16:23480817 | GGTTTGGCAACCAAC[A/C]ATCTCAGTCTTTTCT | 23062 |
rs143774055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489996 | AAGACCCAGGATGCA[A/G]TGCCTGCCTAAGAAC | 23062 |
rs143824255 | in-del | -/CCTGGCACTC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469942 | AGTCCCAGAAAAGAA[-/CCTGGCACTC]AAAAACGACAGCCAT | 23062 |
rs143933289 | snp | C/T | 0.0137329 | 0.0817182 | intron-variant | GGA2 | GRCh38.p7 | 16:23478586 | ACAGCTCTCCTGAGC[C/T]CACCCAAGCTGCTGT | 23062 |
rs143953149 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466413 | CCATCAACAAATATC[C/T]ACCTCTCCTGTCCAG | 23062 |
rs143984316 | in-del | -/A | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501087 | CTCTGGCTATTTTTG[-/A]ACAAGCCAATACACC | 23062 |
rs144070229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23474312 | CATATCCTTGACAGT[A/G]TCAATACTAAGGAAG | 23062 |
rs144226944 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500524 | TGCCAGCCCCAAGCG[A/C/G]GGCAGTGTGCGGGGC | 23062 |
rs144247430 | snp | A/G | 4.95864e-05 | 0.00497903 | missense | GGA2 | GRCh38.p7 | 16:23482955 | TCAGTGGTGTCACTC[A/G]CCAACCGGAACAGCG | 23062 |
rs144352837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498086 | GGAGTTGGAGGCCAG[A/C]CTGGGCAACACGGTG | 23062 |
rs144370069 | snp | C/T | 1.64849e-05 | 0.00287092 | stop-gained | GGA2 | GRCh38.p7 | 16:23474995 | GCCAGCCTCCCAGGA[C/T]CAACCTGGAGAGGAC | 23062 |
rs144462006 | snp | C/T | 8.24056e-05 | 0.00641841 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486048 | GGGCGGGGCCTGCCC[C/T]GGCCTGCGGTACATG | 23062 |
rs144642713 | in-del | -/C | 0.00132048 | 0.0256612 | intron-variant | GGA2 | GRCh38.p7 | 16:23470214 | TAACACCACTACAAA[-/C]CCCCCGGACAGCCAG | 23062 |
rs144674940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489080 | TGAGTGTATGTGACA[C/G]GGAACAACAGTCCAT | 23062 |
rs144737324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23494147 | GAAGGGTGGGGACCC[C/T]GGCCCAGATCTCCCT | 23062 |
rs144833002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503601 | TTATTATCTATTATC[C/T]CATCATTGTTAAATT | 23062 |
rs144903041 | in-del | -/AC | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465373 | GAGTGATGCCATAAA[-/AC]CCACAGCCACTTTCA | 23062 |
rs144966411 | snp | C/G | 0.0126979 | 0.078662 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499703 | TCCTGACCTCGTGAT[C/G]CGCCCGCCTCGGCCC | 23062 |
rs144975430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496695 | GGCGCGATGGCTCAC[A/G]CCTGTAATCCCAGCA | 23062 |
rs145019568 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | GGA2 | GRCh38.p7 | 16:23469257 | TCTGAGACGCAGCAT[C/T]AACAGCCAGGGCACA | 23062 |
rs145026714 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502285 | AAATGAGGCCCCTAC[A/G]TCATGATTATAAAGG | 23062 |
rs145056081 | snp | A/C/T | 0.000263543 | 0.0114767 | missense | GGA2 | GRCh38.p7 | 16:23491706 | ATCTGATAAGCGTCT[A/C/T]GAATCTTGATGTCTT | 23062 |
rs145115965 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23486310 | TGGGTGAAAAAATAC[G/T]CAAAAGCCCAGAGTT | 23062 |
rs145140640 | in-del | -/GTGTGTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511017 | AGACTGGGTTTCACC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 23062 |
rs145142496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23481544 | TTGGGAAGCCAAGGC[A/G]GGCAAATCACTTGAG | 23062 |
rs145211258 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23489728 | TACAGAATTTCTGGA[-/G]GCTGCAACAAAAAGA | 23062 |
rs145336958 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | GGA2 | GRCh38.p7 | 16:23475432 | TGACCTCAGGTGATC[C/T]GTCCGCCTCGGCCTC | 23062 |
rs145408616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490530 | ATTTGAGGTTGGGAG[A/T]TTGAGACCAGCCTGA | 23062 |
rs145476202 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464915 | GGCCTGTGTGTGGAC[A/G]GGAAAGTCCTGAGGA | 23062 |
rs145482996 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | GGA2 | GRCh38.p7 | 16:23506308 | ACCAATGGCCCACCA[C/T]CCCCAACAAATCTGA | 23062 |
rs145597897 | snp | C/T | 0.000905216 | 0.0212553 | intron-variant | GGA2 | GRCh38.p7 | 16:23475102 | GACTAGCAAAAATTG[C/T]AGCGATTTCCTGGAA | 23062 |
rs145743553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480569 | TTAACCCAGAATATG[C/T]TTAGGACCCATTTCT | 23062 |
rs145747722 | snp | C/G/T | 0.000395521 | 0.0140573 | synonymous-codon, missense | GGA2 | GRCh38.p7 | 16:23474917 | ACTGGGCTTAACAGA[C/G/T]TCCAAAGGGACAAAC | 23062 |
rs145829723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23495636 | CTTGAGAGACAAAGG[C/T]CTACACTCAGTGTGG | 23062 |
rs145830611 | snp | C/T | 3.30524e-05 | 0.00406511 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23493451 | TGGTTCATGCACATC[C/T]CCAGCACCTGCACAG | 23062 |
rs145952886 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492492 | ACAAAACAAAAAAAC[C/G/T]TCAGATGAAAACACT | 23062 |
rs145958889 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | GGA2 | GRCh38.p7 | 16:23509885 | AGCCCCAAACAGACT[A/G]CATGTCTTGCACGAC | 23062 |
rs146067806 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493269 | AGGTTTTGTCCATGC[C/G]TGGGCCTGCCTCTGG | 23062 |
rs146084043 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | GGA2 | GRCh38.p7 | 16:23489289 | TCCCAGGCTAGAATG[C/T]AGTGGTGTGATCATG | 23062 |
rs146182398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477789 | TGCCTTTTGCCTTCC[A/G]CCATGACTGGGAGGC | 23062 |
rs146193095 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23473960 | TGCAATCTAACCTCA[A/C]CACAAAGAGCCATAG | 23062 |
rs146205087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468327 | AGACTACAGGCGCAC[A/G]CCACCATGCCCAGCT | 23062 |
rs146227114 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511518 | TTTTTTTTTTTTTCA[A/G]ATGGAGTCTCGCTCT | 23062 |
rs146363257 | snp | A/G | 4.94996e-05 | 0.00497467 | missense | GGA2 | GRCh38.p7 | 16:23480770 | GCCTGGAGAATTTCC[A/G]CTGAAGAATGAGGGA | 23062 |
rs146396049 | snp | A/G | 9.9486e-05 | 0.00705217 | missense | GGA2 | GRCh38.p7 | 16:23468891 | TGGAACATACTTTGT[A/G]TGGATTGTCAAGCAG | 23062 |
rs146414672 | in-del | -/GT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510870 | ACCACCACGCCTGGC[-/GT]GTGTGTGTGTGTGTG | 23062 |
rs146580663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23485850 | TGGGGACTGGGGAGC[A/G]AGGGACAGACAAAGG | 23062 |
rs146698003 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464238 | TCACAGATAAGGAAA[C/T]ATTTTTGCCCAGTCT | 23062 |
rs146709030 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23493429 | GCTGTGGAACTTCTC[C/T]CCACAGTGGTTCATG | 23062 |
rs146740311 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510794 | TCACTGCAGCCTCCA[C/G]CTCCTAGGCTCAAGC | 23062 |
rs146860984 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23490173 | AGATACTGAAGAAAA[C/G]TAACAAACTAGCTAG | 23062 |
rs146865513 | in-del | -/TGTG | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511024 | TTTCACCGTGTGTGT[-/TGTG]GTGTGTGTGTGTGTG | 23062 |
rs146872777 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | GGA2 | GRCh38.p7 | 16:23487127 | GCTGGGACTATAGGC[A/G]CGTGCCACCATGCCC | 23062 |
rs146934935 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491711 | ATAAGCGTCTCGAAT[C/T]TTGATGTCTTCCGGA | 23062 |
rs146944863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488482 | CCTCACTCCTAAGGG[C/T]CTGTCTGGAGAGGAG | 23062 |
rs147039580 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472160 | TTGTAGCCCTGGCAT[C/T]CAAAGATGTTCTTTG | 23062 |
rs147049578 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466015 | GTCTTATGTGAATTA[C/T]GGCAAATGAAATCAC | 23062 |
rs147307607 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466868 | TGAGGCCTGAGTAAG[C/G]CCTGGGAGCTGCTTT | 23062 |
rs147317581 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463679 | TGCATCGCTTGGCTT[C/T]AAAACAAACTGGGGT | 23062 |
rs147402080 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23483343 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAGT | 23062 |
rs147510056 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463275 | CAGCACTTTCAACAC[A/G]TAAGTGCTTGATTTG | 23062 |
rs147519965 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | GGA2 | GRCh38.p7 | 16:23508767 | TGCCCTCTCCAGTGC[A/C]AACCAGCTGCCTAGA | 23062 |
rs147529603 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504589 | AAGACTTGAGCAGCT[A/C/G]CAAAAAATGACCCCC | 23062 |
rs147618291 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23486251 | GAGAGAGCTCGCTCA[-/G]GGGGCATCACCAGGA | 23062 |
rs147643773 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23480199 | CTGACCACAGCTGAT[G/T]AGAATCACCCACAGT | 23062 |
rs147679405 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | GGA2 | GRCh38.p7 | 16:23475472 | TGGGATTACAGGCGT[C/G]AGCTAATGCGCCAGA | 23062 |
rs147821763 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486075 | CATGCTCAGCATCTC[C/T]TGCAGCACCTTCACA | 23062 |
rs147851283 | snp | A/G | 1.65853e-05 | 0.00287964 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23475034 | TGGTGGCACTTCCTT[A/G]GGGACACTTTTCTGC | 23062 |
rs147959774 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499900 | GCGGGGCCTGGTGAA[C/G]CACGTGCCTAGGCTC | 23062 |
rs147977624 | snp | C/T | 0.000732832 | 0.019128 | missense | GGA2 | GRCh38.p7 | 16:23478416 | TCCAGCAAATTCCTG[C/T]CTGCAGAAGGGTTCT | 23062 |
rs148053957 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23496193 | CTGTAATCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 23062 |
rs148107863 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504281 | TTTCTAACCACTCTT[C/G]CGGTGAGGTCTTCAG | 23062 |
rs148171125 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | GGA2 | GRCh38.p7 | 16:23492609 | TGTCCCCTCTTGCCC[C/T]ACCAAGACCTTGCCT | 23062 |
rs148172898 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | GGA2 | GRCh38.p7 | 16:23472928 | GTCCCAGCTACTCGG[A/G]AGGCTGAGGCAAGAG | 23062 |
rs148204259 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23488344 | ACTGGGGTAAGGCAG[G/T]ATCACAAACAGATCC | 23062 |
rs148325586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476913 | AGCAGGTATTTTCCT[A/C]CGACTTAGGAAAAGA | 23062 |
rs148356247 | snp | C/G | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23467657 | TCGCTGAAAGGCTGT[C/G]CACCTTGGTTGAATG | 23062 |
rs148447611 | in-del | -/GC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470824 | AAAAATGAAATAAAT[-/GC]TTTTTTTTTTTTTTT | 23062 |
rs148510857 | in-del | -/AAAG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475952 | AAAAAGAAAAAAACA[-/AAAG]AAAGCACTTAAAATG | 23062 |
rs148636821 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464172 | TTTTCTTTTGGTTGT[C/T]ATTTATTGTTTTCAA | 23062 |
rs148723605 | snp | A/C/T | 0.000132242 | 0.00813062 | missense | GGA2 | GRCh38.p7 | 16:23482961 | GTGTCACTCGCCAAC[A/C/T]GGAACAGCGTGGGCC | 23062 |
rs148816426 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | GGA2 | GRCh38.p7 | 16:23491046 | AAAAAATACAAATAT[G/T]TGGTGTAAGTGAGAC | 23062 |
rs148900700 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510849 | GGAGCTGGGACTAGG[C/G]GAGGGCACCACCACG | 23062 |
rs148964489 | snp | A/G | 4.94662e-05 | 0.00497299 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480669 | CAGGGATGTCTCCCA[A/G]TGAGCTGGTCACTCT | 23062 |
rs148970262 | in-del | -/GATTG | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483637 | CTGTGGTTTCTTTTT[-/GATTG]TTTGTTTTTTTGGTT | 23062 |
rs149013892 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23487439 | ATCCTACAGTGCACA[C/G]GACAGTCCCCAACAA | 23062 |
rs149111450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23469918 | TCTTTCCTTGACACT[C/T]GACAGGTAAGTCCCA | 23062 |
rs149141187 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | GGA2 | GRCh38.p7 | 16:23507669 | GCCGGTTGTGGTGGC[A/G]TGTGCCCGTAATCCC | 23062 |
rs149375289 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466005 | ATTAAAATTCGTCTT[A/G]TGTGAATTATGGCAA | 23062 |
rs149406164 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | GGA2 | GRCh38.p7 | 16:23472772 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23062 |
rs149610585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498028 | GCTCATGCCTTAATC[C/T]TAGCACTTTGGGAGG | 23062 |
rs149663323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23505393 | TACCAACAGGGACCC[A/G]GTTAAATGGATCCTA | 23062 |
rs149724323 | snp | C/G | 1.81223e-05 | 0.00301012 | intron-variant | GGA2 | GRCh38.p7 | 16:23475083 | AGAAATAAAAAATAT[C/G]AAAGACTAGCAAAAA | 23062 |
rs149792096 | snp | A/G | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23470156 | TACACAATGAGAGGC[A/G]GCAGGCTGCCTGGTA | 23062 |
rs149873934 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464027 | CATCTTCTATAATGG[C/G]TATATTTAAAGGATT | 23062 |
rs149952041 | snp | A/G | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23486750 | CGGTTTGCAGCCTGA[A/G]GGTCCTCGGGGTGGT | 23062 |
rs150020918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485707 | TGCTACACACAGCAA[C/T]GTGAATGGATCTCGA | 23062 |
rs150030103 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510907 | AGACTGGGTTTCACC[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 23062 |
rs150096173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482832 | AACCGAAAGTCCACT[C/T]TGTCTTGTTCCTGGC | 23062 |
rs150117942 | snp | C/T | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23479828 | TCTGCGCAGGTCCAT[C/T]GTCCACCTCCAAGTC | 23062 |
rs150188253 | snp | C/T | 0.0209421 | 0.100162 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465662 | AAGCTACACAGAGGC[C/T]GGGTGCGGTGGCTCA | 23062 |
rs150275766 | snp | A/C/T | 0.000561233 | 0.0167431 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494366 | GGCCAGTAGCCAGGG[A/C/T]GCATGTGTGGGGCTA | 23062 |
rs150348382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502189 | AAGAGAGAGTGGCAT[C/T]GGGGCAAGGCTGTCA | 23062 |
rs150401967 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | GGA2 | GRCh38.p7 | 16:23507571 | AGGCGGACGTTGCAG[A/T]GAGCTGAGATCGTGC | 23062 |
rs150506763 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23467872 | GGGAACCCTTCGATA[A/G]TTCTGCAGTCCTGAA | 23062 |
rs150560663 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | GGA2 | GRCh38.p7 | 16:23474375 | ACTTTTTTTTTTTTT[A/G]GAGACGGAGTCTCAC | 23062 |
rs150611801 | snp | C/T | 1.66441e-05 | 0.00288474 | missense | GGA2 | GRCh38.p7 | 16:23468993 | GCAGCTTCACTCTCA[C/T]TGACTATCAGGGGAA | 23062 |
rs150664872 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504339 | GGAAGCCAGCTTGAT[C/G]TTCGTGCTCATAAAC | 23062 |
rs150778480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479282 | CTTCCTGAGGAGACC[A/T]GCTCACTCCCCTACT | 23062 |
rs150786138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492978 | TGTTGGTTACCTGAG[A/T]CTGGCTGAGCTAAGA | 23062 |
rs150854450 | snp | A/C/T | 0.00011543 | 0.0075963 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486036 | GGCCTCCTGGTCGGG[A/C/T]GGGGCCTGCCCTGGC | 23062 |
rs151001139 | snp | C/T | 0.0399052 | 0.1355 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464983 | GAAAAAGAGCAGTCA[C/T]GGAGGTAGGTCACGA | 23062 |
rs151011223 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511869 | AAAAGGAAGATAAGA[C/T]GAATGTGCAAATGGA | 23062 |
rs151107060 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | GGA2 | GRCh38.p7 | 16:23494584 | CAGCACCCAAGGTCC[C/T]CCTCCTGCCCAGGGC | 23062 |
rs151161044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501082 | ATAGATCTCTGGCTA[C/T]TTTTGACAAGCCAAT | 23062 |
rs151167188 | in-del | -/CT | 0.01305 | 0.0797164 | intron-variant | GGA2 | GRCh38.p7 | 16:23508937 | ATTTCTCCTTGTCCC[-/CT]GTCTGCATTCCAAGG | 23062 |
rs151255847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484605 | ACATGTCTTCTAAGA[C/T]GCACAAGCTGCCAAT | 23062 |
rs180692556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507397 | CTTCGGGAGGCCAAG[A/G]CTGGCAGATAACTTG | 23062 |
rs180879892 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23484333 | TGAGGCAGGAGAATC[A/G]CTCGAACCCGGGAGG | 23062 |
rs180941594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23468402 | AGGATGGTCTCGATC[A/G]CTTGATCTCGTGATC | 23062 |
rs180961600 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511451 | GGGGTGAGCCACCAC[A/G]CCCGGCCTATGTGCT | 23062 |
rs180974572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490457 | AATAAATCCACAGCC[A/G]GGAGCGGTGGCTCAC | 23062 |
rs181012358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481542 | CTTTGGGAAGCCAAG[A/G]CGGGCAAATCACTTG | 23062 |
rs181058100 | snp | A/G | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23504947 | CATCCAAGAGTGACT[A/G]ATTCAGAAGCCAAAC | 23062 |
rs181224539 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23468209 | TATTTGATAGAGTCT[C/T]GCTCTGTCACCAGGC | 23062 |
rs181348363 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504282 | TTCTAACCACTCTTG[C/T]GGTGAGGTCTTCAGT | 23062 |
rs181426729 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481261 | GCCTGTAATCCCAGC[C/T]ATTCGGGAGGCTGAG | 23062 |
rs181473881 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511878 | ATAAGACGAATGTGC[A/T]AATGGAGGCAAAACT | 23062 |
rs181486717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23469254 | GCATCTGAGACGCAG[C/T]ATCAACAGCCAGGGC | 23062 |
rs181588047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504018 | CCCGGGAGACGGAGG[C/T]TGCGGTGAGCCAAGA | 23062 |
rs181597418 | snp | A/G | 6.60295e-05 | 0.00574547 | missense | GGA2 | GRCh38.p7 | 16:23480650 | TCAAACATACCTCTG[A/G]AGACAGGGATGTCTC | 23062 |
rs181620688 | snp | A/G | 0.000168183 | 0.0091686 | intron-variant | GGA2 | GRCh38.p7 | 16:23491838 | ATTCTAGAGCTGGAA[A/G]GGACTTGGGAGACCG | 23062 |
rs181701751 | snp | A/C | 0 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23498685 | GTAAGAGGTCTACAA[A/C]GGATAATTGTTTATT | 23062 |
rs181710764 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507212 | ACTTCTGAAAACCCA[C/T]GATATTTCACTTAAG | 23062 |
rs181719373 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23473086 | ACCTCTACTTAATAG[A/T]GCATATATATATAAG | 23062 |
rs181943656 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23507541 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 23062 |
rs181956282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484934 | AGTCATTATTCGTAA[C/T]GAATAATTCAAAGGC | 23062 |
rs182092539 | snp | C/T | 0.000458707 | 0.0151375 | intron-variant | GGA2 | GRCh38.p7 | 16:23475105 | TAGCAAAAATTGTAG[C/T]GATTTCCTGGAATCT | 23062 |
rs182100228 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499176 | TTGATATGGAGTCTC[C/G]CTCTGTCACCCGGGC | 23062 |
rs182125174 | snp | C/G | 0.000646935 | 0.0179736 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465440 | CTGTCCAACACCTAA[C/G]CATAGTAGTACCACT | 23062 |
rs182172151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23497644 | CTTAAAATCCTATCT[A/G]CCCTTGAGTCCCAAG | 23062 |
rs182383827 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508028 | CTCCTTTTATCTCCT[C/T]CACCTGAGGCAGCTA | 23062 |
rs182442094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23493647 | GTCCCCTGTTCAATC[C/T]TGCTATAACTGCCTG | 23062 |
rs182452826 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472570 | TTAATAAGCTGGACA[C/T]AGTGGCGCATGCCTG | 23062 |
rs182464792 | snp | G/T | 0.000124176 | 0.00787862 | intron-variant | GGA2 | GRCh38.p7 | 16:23469986 | GAGAAATCCCCAACA[G/T]ATGACTCACCTTTGG | 23062 |
rs182636460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486479 | TGTCTAGGAAATGCT[C/T]TGAGCAGCATGGATG | 23062 |
rs182744764 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23482495 | ACTGTGGACAATTCT[C/G]CACTTCCTTACAGAT | 23062 |
rs182745738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23492377 | GGGGGGTGTGAACTA[C/G]AGATTGAGTTCAACT | 23062 |
rs182750421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505468 | ACAAGGCGGCTACAT[A/C]TGCAGTCATGTGGAA | 23062 |
rs182760333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469379 | GGTAGTAGCAGAACA[C/T]TGCCCATAGGACTAC | 23062 |
rs182874195 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23505552 | ATGCACAGGCGCTGC[C/T]GTTTGTACTTTTAAG | 23062 |
rs183025254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23477827 | GCCACATGGAACTAT[A/G]AGTCCATTAAACCTC | 23062 |
rs183060548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500328 | CCAGGAGCCGAGCTG[A/C]CTCACGGGGAACATG | 23062 |
rs183190496 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23482871 | GTGACAGGAGGGACC[A/G]AGTCTGTCTTGCACC | 23062 |
rs183252411 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | GGA2 | GRCh38.p7 | 16:23470624 | AAAAATTAGCTGGGC[A/G]TGGTGGTACACACCT | 23062 |
rs183294501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23487952 | CATGACCAAAAGCAC[C/T]GCCAGCACTAGGCCA | 23062 |
rs183319779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23509443 | CGCCCTCCTCCTCCT[C/T]GCCAATCCCGTTAGT | 23062 |
rs183497006 | snp | A/G | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502831 | TCCAAAATAGAAAGT[A/G]CTGAGGATCAACTGC | 23062 |
rs183505999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468298 | TTCTCCTGCCTCACT[C/T]TCCCGAGTAGCTGAG | 23062 |
rs183529750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23489788 | AACAGCGGGAAGGCC[C/T]GAAGGCGGGATTAGG | 23062 |
rs183540080 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23495904 | CAGTGGGCAGACAGC[C/T]GGAAGGAGAGGAATT | 23062 |
rs183609156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485615 | CAAAGCTGGAAACAA[C/T]GCAAGGCCCATCAAC | 23062 |
rs183637954 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497006 | CATGTGACTGTAGTC[A/C]CAGCTACTCAGGAAG | 23062 |
rs183787945 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500098 | TCAGGCTTGTTGTAT[C/G]TAGACCCATTCTAAG | 23062 |
rs183816356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507675 | TGTGGTGGCGTGTGC[C/T]CGTAATCCCAGCTAC | 23062 |
rs183823768 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23464076 | AGGCAAGCACTATTT[C/G]TATTCTAGAATATTG | 23062 |
rs183901202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471412 | ATAAATTTAAAAAGG[A/G]GGGCAGGGCTATAGC | 23062 |
rs183935708 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23496685 | ATTAAGACCAGGCGC[A/G]ATGGCTCACGCCTGT | 23062 |
rs184171320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479053 | TCATGTGACTCGTCC[A/G]TGGCCAATCTGTGAC | 23062 |
rs184214082 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510688 | ATTTGATTTTCAGAA[A/G]AACACGAATAATTCT | 23062 |
rs184393026 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | GGA2 | GRCh38.p7 | 16:23483655 | TGTTTGTTTTTTTGG[G/T]TTTTTTTTGAGACAG | 23062 |
rs184402460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23506268 | TACTATCAATCCCAC[A/G]ACCCCCTTATCCCTC | 23062 |
rs184544863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504132 | TACCATGCCAGATGT[C/T]CTCAGAACAATCCAG | 23062 |
rs184547095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23483392 | CCAGCTACTCGGGAG[A/G]CTTTCTCTTAGGAAT | 23062 |
rs184664376 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505920 | TACTCTGGGACTTTC[C/T]TTACTTTCCTTTTTT | 23062 |
rs184717925 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23507214 | TTCTGAAAACCCACG[A/C]TATTTCACTTAAGAA | 23062 |
rs184818235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484191 | GACGGGTGGATCACC[C/T]GAGGTCAGGAGTTCG | 23062 |
rs184833786 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466987 | TCATGGCAGCCACTC[A/G]CCTGGGAACAGTGCA | 23062 |
rs185118863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23484342 | AGAATCGCTCGAACC[C/T]GGGAGGCAGAAGTCG | 23062 |
rs185304729 | snp | A/C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509757 | ACACATATATATATA[A/C/T]ACGCACACACACACA | 23062 |
rs185352942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23488860 | CACCCAGTGTATGAA[C/T]GAAGTTTTGCATCAT | 23062 |
rs185467966 | snp | C/T | 0.000208286 | 0.0102029 | missense | GGA2 | GRCh38.p7 | 16:23467690 | AGCTTGTACCGTAAG[C/T]GGATAGGTTCCTGGG | 23062 |
rs185491156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503167 | TTGTGTTTGCTTTCA[C/T]AATACAGTGGTTTGG | 23062 |
rs185632543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480225 | ACAGTGCTTGAAAGA[C/T]GCACACCTCCAGGCC | 23062 |
rs185662114 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498705 | AATTGTTTATTATTA[C/T]GTACAGTCTCTGGCT | 23062 |
rs185676925 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23474633 | ATTTTTTTCTTCCCC[C/G]CCAAATAGAGACAAG | 23062 |
rs185748907 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463320 | AGGGAAGAGAGCGGG[A/G]TTATGTTTCTAAGTA | 23062 |
rs185802281 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23493230 | GAGCTTGGAGAGGAG[A/C]GCGCTTCTTTCACAG | 23062 |
rs185815714 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469667 | CCGGTGAGAGTTTCT[C/G]AGATAAAGAGGGTTA | 23062 |
rs185833532 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23481341 | TCGCACCATTGCACT[C/T]CAGCCGGGGCAGCAA | 23062 |
rs186019250 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499287 | GTAGCTAGGATCACA[A/G]GTGCCCACCAACATG | 23062 |
rs186116343 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | GGA2 | GRCh38.p7 | 16:23475293 | CTCCCAGGCTCAAGC[A/G]ATTCTCCTGACTCAG | 23062 |
rs186132721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507456 | AACATGGTGAAACCC[G/T]ATCGCTACTAAAAAT | 23062 |
rs186192750 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23468815 | AATGTGCCTCTCTCT[A/G]CCCACAAAGTTACCT | 23062 |
rs186213181 | snp | C/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511566 | GCAGTGGTGCTATCT[C/T]GGCTCATTGCAACCT | 23062 |
rs186226352 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23491119 | TGTTTGTGTGTGTGT[A/G]TTGGGGTGTGGGTGG | 23062 |
rs186331686 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23507754 | GCAGAGAGCCGAGAT[A/G]GCACCACTGCACTCC | 23062 |
rs186372644 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23507564 | ACCTGGGAGGCGGAC[A/G]TTGCAGTGAGCTGAG | 23062 |
rs186385604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23484972 | ATAATAGCCAAAAAG[C/T]AGGAACAACCCAAAT | 23062 |
rs186645456 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | GGA2 | GRCh38.p7 | 16:23472734 | AAAATAAAATAATTT[A/T]AAAAAAAAGACTGAA | 23062 |
rs186689821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504790 | GCTGGCACTTGAGCA[A/G]GACAGAGGGGTGCTG | 23062 |
rs186782905 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492032 | CATGCAAGAGCCTGG[A/G]TCAGAGCCTGTTCTA | 23062 |
rs186835039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487145 | TGCCACCATGCCCAG[A/C]TAATTTTTGTGTTTT | 23062 |
rs186838541 | snp | A/C/G | 0.000144149 | 0.00848867 | intron-variant | GGA2 | GRCh38.p7 | 16:23478329 | AGGAACCGCACTCAG[A/C/G]AGCCACACTCTCCCA | 23062 |
rs186845363 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500888 | GAAAATATCAAATGA[G/T]TGTGCAAGAAAAGAG | 23062 |
rs186848501 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23498116 | GAAATCCCGTCTCTA[C/T]CAAAATACAAATAAT | 23062 |
rs186851334 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508921 | CCGCGATCTAGCCTA[G/T]ATTTCTCCTTGTCCC | 23062 |
rs186862795 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466285 | GCCATCTCAGCCAGG[C/T]TCAGGTTCCTTCTCC | 23062 |
rs187001293 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511932 | TGTCCCTCCAGTGAG[C/T]GGAATTTACCTATTT | 23062 |
rs187010067 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23469288 | TCTTGGGTTGAATTC[A/T]AACTGCTTCTCACTA | 23062 |
rs187176464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505065 | TGAGGAAGTGGTCAC[C/T]CCGAGGAGCAGAATG | 23062 |
rs187346040 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | GGA2 | GRCh38.p7 | 16:23481618 | TCTCTACTAAAAGTA[A/C]AAAAATTAGCCAGGT | 23062 |
rs187436775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23482529 | CCTTCCATTTCCCAT[C/T]GGCCTGGCCCTCTTA | 23062 |
rs187440152 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23505514 | ATGAAGTGGAAAAAA[A/C]CACCACAGAACTGAA | 23062 |
rs187662173 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23502887 | TCTGAGACTTTCTTT[G/T]TTTCTTACAAGAACA | 23062 |
rs187684272 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483426 | GAAAGACAGTAGTTC[A/C]TTTCTACTAATCTTG | 23062 |
rs187881142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23494769 | CAAACTGGCCAAATA[C/T]GCGACACCACACAGA | 23062 |
rs187957317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479537 | ACTCTCCCTGACTTG[A/C]TCAGCAGCAGACACG | 23062 |
rs187972466 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465152 | GTAGCTGGTCAACAA[C/G]TAGCTTTTAAAAAAA | 23062 |
rs188024837 | snp | A/G | 6.61802e-05 | 0.00575202 | intron-variant | GGA2 | GRCh38.p7 | 16:23488721 | ATTCCTAAAAATGCA[A/G]TTTACAAAGTTAAGA | 23062 |
rs188055401 | snp | C/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510870 | CACCACCACGCCTGG[C/T]GTGTGTGTGTGTGTG | 23062 |
rs188056960 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509478 | TGATGTGACTGCCGG[A/C]TTGTACCCACTAAAA | 23062 |
rs188070644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23489977 | ATCACAAACAGATCC[C/T]ACCAAGACCCAGGAT | 23062 |
rs188122815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23483198 | CTACAGGCTACAAGT[A/G]TATGATTTCTGAAAA | 23062 |
rs188240605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468320 | GTAGCTGAGACTACA[A/G]GCGCACGCCACCATG | 23062 |
rs188262438 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486147 | CTTCTCCGATTTTTC[C/T]TGTTCCTTTTGGGAA | 23062 |
rs188392438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23505553 | TGCACAGGCGCTGCC[A/G]TTTGTACTTTTAAGG | 23062 |
rs188464185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23496433 | CCACCTGGCCTGTGA[C/T]AAGCGGAGACAGAAG | 23062 |
rs188505180 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23481237 | TACAAAAAATCAGCC[A/G]TGGCAGGTGCCTGTA | 23062 |
rs188517140 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504279 | TGTTTCTAACCACTC[C/T]TGCGGTGAGGTCTTC | 23062 |
rs188585320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23506009 | GATAATAATAGCTAG[C/T]GCTTCTTGGGCACTT | 23062 |
rs188680236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23471602 | TCAAAATATACATTA[C/T]TAAAATATAGCTTAG | 23062 |
rs188712322 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | GGA2 | GRCh38.p7 | 16:23470882 | TTGCCCAGGCTGGAA[C/T]GCAATGGCATGATCT | 23062 |
rs188713467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23496784 | CAACATGGTGAAACC[C/T]TGTGTCTACTAAAAA | 23062 |
rs188751525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470308 | AATTCCTCTGCACTA[C/T]CATAATCCAAGTCCT | 23062 |
rs188881722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23476736 | CAACCTTGTTTTTAG[A/G]GAGTGGCACTTTGCA | 23062 |
rs188989025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507120 | ATGAAAAACAGCTGA[A/G]GAGGCCACTGGCTGC | 23062 |
rs189148526 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23483724 | TGATCTCAGCTCACC[A/G]CAACCTCCGCCTCCT | 23062 |
rs189199172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500146 | CAAGGGACCCTTGTA[C/G]ACAAGGCAGCTCAGG | 23062 |
rs189202877 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467308 | AAACATGACTGTAGC[A/C]GAGATGATGATGATG | 23062 |
rs189373630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23468051 | AAGACAGACTCCAGC[A/G]AGGGATATTCCACAT | 23062 |
rs189502272 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511796 | TACATGAGGGAACCA[A/G]GCAGATGTTATAATC | 23062 |
rs189625763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480283 | GTCCAAGCCAGGGAC[C/T]GCATTTCAACCAGTG | 23062 |
rs189690902 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23489196 | AACTATCACCCCCAT[A/C/T]GTGACAACAACAAAA | 23062 |
rs189755188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23484275 | AATACAGAATTAGCC[A/G]GGCGTGCTGGCACAT | 23062 |
rs189780538 | snp | A/C | 2.22442e-05 | 0.00333491 | intron-variant | GGA2 | GRCh38.p7 | 16:23493512 | CAGTGGTCCCAGGCT[A/C]CCCTCCAGGCTGGTA | 23062 |
rs189797084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469885 | CCCACTTTATCTTCA[C/G]TTAGTTTGAGTGAAG | 23062 |
rs189894414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498264 | CAGCCTGGGTGACAA[A/G]GTGAGACTCTGTCTC | 23062 |
rs189985394 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GGA2 | GRCh38.p7 | 16:23505546 | GACAGAATGCACAGG[C/T]GCTGCCGTTTGTACT | 23062 |
rs190001657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482577 | CTGAAGGTACAAAAG[C/T]CCGTGATCCCCTTGA | 23062 |
rs190037636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507259 | GTTCCTGAAAAACAG[A/G]AAGATCTAGCAACTT | 23062 |
rs190161597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472801 | GCACTTTGGGAGGCC[G/T]AGGTGGGCAGATCAC | 23062 |
rs190230237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23472541 | TAGAAAGAAATTGAC[C/T]TTCAGAGAAGGACTT | 23062 |
rs190421364 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23474794 | AAAATCTCTCCCATT[A/T]ATCAACCAAATTTAA | 23062 |
rs190427842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499058 | AGAGAACAGGAGGCA[C/T]GGCCCAAGCTCCCCT | 23062 |
rs190428174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23507573 | GCGGACGTTGCAGTG[A/G]GCTGAGATCGTGCCA | 23062 |
rs190447073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23485527 | CCCAGACATTTACCC[A/T]TAAGAAATGAAAATC | 23062 |
rs190470757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500304 | AAGGCCCAAGCTACC[A/G]GAGAGGAGCCAGGAG | 23062 |
rs190484608 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23497311 | TTCCTCTCAGTGCCC[C/T]ATCCATATTCTTCCA | 23062 |
rs190585536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23491433 | ATGCTGTGGTTTCCT[A/G]TGATTTCCAGGCAAC | 23062 |
rs190723346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23504870 | TGATTCATTTCAAGC[A/G]TGCTACAGGGCCAGA | 23062 |
rs190758935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23484590 | AATGGATTTGCACAG[A/C]CATGTCTTCTAAGAT | 23062 |
rs190769117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507465 | AAACCCTATCGCTAC[C/T]AAAAATACAAAAATT | 23062 |
rs190792295 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503425 | GATATTTTCTTTTTT[A/C]TCTTTACTTGTAAGA | 23062 |
rs190827792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23469164 | GCAGACAGACTCCCA[C/T]TAATTGATAAAAGGA | 23062 |
rs190906587 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23481688 | TGAGGCATGAGAATC[A/G]CTTGAACACAGGATG | 23062 |
rs190910987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505133 | CCCTGGGAGGGACAC[A/G]TGGACCCCAAGAGTC | 23062 |
rs190939910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481420 | GAGCAGCATCATGGG[A/G]GATGCCACGAGCAAA | 23062 |
rs191040810 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512044 | AAGGTTGTGCTGTCT[A/G]GACAACACATAATTT | 23062 |
rs191046511 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23469363 | TAACTTATAAAACAG[A/T]GGTAGTAGCAGAACA | 23062 |
rs191208440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23486397 | ACCAGCCTCAAGTCC[C/T]CTGAAAAGCAGATTC | 23062 |
rs191272591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472050 | GAAATTGGTAATGCA[C/G]ATCAAAATTTTAAAT | 23062 |
rs191275608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23492266 | GCTGGCCACTCCAAA[A/G]AGATCAACCTTGTGA | 23062 |
rs191279007 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23496887 | TGCCTGAACCCAGGA[A/G]GTGGAGGTTGCAGTG | 23062 |
rs191429462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23507968 | CTGTTTCAAAAAAAG[C/T]TGGAGTTGAAGAACT | 23062 |
rs191432670 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465362 | CTGATTAGAAGGGAG[C/T]GATGCCATAAACCAC | 23062 |
rs191489282 | snp | A/G | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463413 | ACAGAACAGTATACT[A/G]TATTTTCTTGAACAT | 23062 |
rs191560454 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | GGA2 | GRCh38.p7 | 16:23470976 | CTGGGATTACAGGCA[G/T]GCACCACCACGCCTG | 23062 |
rs191719185 | snp | C/T | 0.0002398 | 0.0109473 | intron-variant | GGA2 | GRCh38.p7 | 16:23478936 | AGGAGTAGAGTGAGA[C/T]GCCTAACAGTAACTC | 23062 |
rs191734984 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501675 | ATCTTAAAGAGAGAA[A/G]TTAACATTATAAGAT | 23062 |
rs191836922 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | GGA2 | GRCh38.p7 | 16:23475437 | TCAGGTGATCCGTCC[A/G]CCTCGGCCTCCCAAA | 23062 |
rs192026728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477275 | AAATCTCATCTTGAA[C/T]TGTAGCACCCACAAT | 23062 |
rs192176341 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499889 | CCGCTGGCAGGGCGG[A/G]GCCTGGTGAACCACG | 23062 |
rs192272297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23505562 | GCTGCCGTTTGTACT[C/T]TTAAGGCATGAGATT | 23062 |
rs192421374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487190 | TTTCACCATGTTGGC[C/G]AGGATGGTCTCAATC | 23062 |
rs192439245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479618 | CCTCAGCAGCAAGCA[C/T]GTGCTCCCAGAGGGA | 23062 |
rs192439686 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466339 | TGTCAAACATACACA[C/T]TCAAGTTCCTAGCAC | 23062 |
rs192538851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23483505 | CCTCCTGTGCAGAGA[C/G]ACATAAAAAACTGGA | 23062 |
rs192547463 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506226 | ACCCATGAGCTTTTG[C/T]CTTCAACTACACCCA | 23062 |
rs192700930 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | GGA2 | GRCh38.p7 | 16:23483309 | GTCAGGAGTTCAAGA[A/C]CAGCCTGGCCAACAT | 23062 |
rs192736311 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GGA2 | GRCh38.p7 | 16:23489519 | TGCTGGGATCACAGG[C/T]GTGAGCCACCATGCC | 23062 |
rs192767355 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503131 | TTTTATCGGGAACAA[C/G/T]AGGAATCCCTATTTT | 23062 |
rs192880525 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467503 | GGACTCTTGGCACTC[C/T]GCACTGAAACACCGT | 23062 |
rs192899602 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23509580 | GGGGAATATTCTTTA[G/T]CCCCTTTGAACCTCA | 23062 |
rs193100017 | snp | C/T | 8.27821e-05 | 0.00643306 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495753 | TGACCAATCCTGTTC[C/T]GACATGCTTGGGTCT | 23062 |
rs193184002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23496621 | CCCAGGAGTTTGAGA[C/T]CAGCATGGGCAACAT | 23062 |
rs193253529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470405 | CACACCACCAGTTAT[C/T]AAAAATCACATTTTT | 23062 |
rs199515488 | in-del | -/GC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480604 | TGGGAATTACAGGCT[-/GC]CCCAAGGCAGAGAAG | 23062 |
rs199525199 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468560 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 23062 |
rs199538482 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495087 | TCTCAGGAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 23062 |
rs199629418 | snp | A/C/G | 0.00299551 | 0.0385847 | intron-variant | GGA2 | GRCh38.p7 | 16:23480607 | GAATTACAGGCTGCC[A/C/G]CAAGGCAGAGAAGGC | 23062 |
rs199705736 | snp | A/C/G | 7.70971e-05 | 0.00620834 | synonymous-codon, missense | GGA2 | GRCh38.p7 | 16:23467604 | GTTAGGCTGCGCCCA[A/C/G]GACAGCCAGGTCTGG | 23062 |
rs199739748 | snp | A/C/T | 8.27526e-05 | 0.00643197 | intron-variant | GGA2 | GRCh38.p7 | 16:23493325 | CAGTGGGCGTAGGTG[A/C/T]GACACAGTCAGCAGA | 23062 |
rs199770832 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465876 | AACCTGGTAGGCAGA[A/G]ATTGCAGTGAGCTGA | 23062 |
rs199860431 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475947 | GAAAAAAAAAAGAAA[A/C]AAACAAAAGCACTTA | 23062 |
rs199872843 | snp | A/C/T | 4.95302e-05 | 0.00497625 | synonymous-codon, missense | GGA2 | GRCh38.p7 | 16:23479781 | CAAGGCTGCCAGGTC[A/C/T]TGATGAAGCAAAGAT | 23062 |
rs199899713 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500740 | GTGGCAGTAGCGCCA[C/G]ACCCCACTGCTGTGG | 23062 |
rs199927740 | in-del | -/ACACACACACACACACAC | | | cds-indel | GGA2 | GRCh38.p7 | 16:23467388 | CCACCCTCTCCCCGA[-/ACACACACACACACACAC]ACACACACACACACA | 23062 |
rs200011706 | snp | A/G/T | 8.2876e-05 | 0.00643677 | intron-variant | GGA2 | GRCh38.p7 | 16:23486183 | GGAGGATGGGAGTGA[A/G/T]GGAGCAGAAACCCTG | 23062 |
rs200012552 | snp | C/T | 0.000231004 | 0.0107447 | missense | GGA2 | GRCh38.p7 | 16:23486032 | GCAGGGCCTCCTGGT[C/T]GGGCGGGGCCTGCCC | 23062 |
rs200022066 | in-del | -/TT | 0.0123036 | 0.0774623 | intron-variant | GGA2 | GRCh38.p7 | 16:23470856 | TTTTTTTGGACAGAC[-/TT]TCGCTTTTGTTGCCC | 23062 |
rs200028402 | snp | C/G | 3.33439e-05 | 0.00408299 | intron-variant | GGA2 | GRCh38.p7 | 16:23468853 | CAGTTCAGGGGCCCC[C/G]ATCTCCCTGCTACCA | 23062 |
rs200089539 | in-del | -/AA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473562 | CGAACTCCTGACCTC[-/AA]GTGATCTGCCCACCT | 23062 |
rs200101723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471068 | CAGGCCTCAAACTCC[C/T]GACCTCAGGTGATCC | 23062 |
rs200136612 | snp | C/T | 0.000790475 | 0.0198649 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486099 | CTTCACATGGCTTCG[C/T]ACTTCCTCCACCGCA | 23062 |
rs200155355 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506893 | CTCTGTGAGGCCAGG[C/T]CCCCCTTTTTGCTCT | 23062 |
rs200173946 | in-del | -/AAAAG | 0.426201 | 0.177351 | intron-variant | GGA2 | GRCh38.p7 | 16:23495088 | CTCAGGAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAC | 23062 |
rs200191754 | snp | A/G | 0.00026466 | 0.0115004 | intron-variant | GGA2 | GRCh38.p7 | 16:23493321 | TTGACAGTGGGCGTA[A/G]GTGCGACACAGTCAG | 23062 |
rs200257802 | snp | A/C | 7.20786e-05 | 0.00600284 | intron-variant | GGA2 | GRCh38.p7 | 16:23478317 | TGTCCCATGAGAAGG[A/C]ACCGCACTCAGGAGC | 23062 |
rs200346354 | snp | A/G | 1.65389e-05 | 0.00287562 | missense | GGA2 | GRCh38.p7 | 16:23479848 | ACCTCCAAGTCAATC[A/G]GGGGGCAGGTCTTCA | 23062 |
rs200357653 | snp | A/C/G | 5.15108e-05 | 0.00507476 | missense, synonymous-codon | GGA2 | GRCh38.p7 | 16:23470020 | AGCCACTTGAAACAT[A/C/G]ATATCCCAGACAGGC | 23062 |
rs200373217 | snp | C/T | 8.23961e-05 | 0.00641804 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474962 | TGTATTCTGTGAAGA[C/T]GGGGAAGGAGCCAAC | 23062 |
rs200433147 | snp | A/C/G | 0.00167828 | 0.0289199 | intron-variant | GGA2 | GRCh38.p7 | 16:23474867 | AATAGATTCCCAGGG[A/C/G]AAAAAAAAAAAAGGT | 23062 |
rs200436410 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | GGA2 | GRCh38.p7 | 16:23486836 | GACCACAACTCCCTC[A/G]GGCCTAGAGCAGAAG | 23062 |
rs200514330 | in-del | -/CCC | 0.0141031 | 0.0827807 | intron-variant | GGA2 | GRCh38.p7 | 16:23480605 | GGGAATTACAGGCTG[-/CCC]CAAGGCAGAGAAGGC | 23062 |
rs200560596 | snp | A/C | 0.000165033 | 0.00908236 | missense | GGA2 | GRCh38.p7 | 16:23479800 | TGAAGCAAAGATGGC[A/C]CCACAGTCCCCATCT | 23062 |
rs200664276 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470740 | AGTGACAGAGCGAGA[C/G]TCTGTCTCAAACAAA | 23062 |
rs200697808 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467217 | GATGAATGGAACGAA[C/T]GATACATGAAAAAAA | 23062 |
rs200722860 | snp | A/G/T | 5.44354e-05 | 0.00521682 | intron-variant | GGA2 | GRCh38.p7 | 16:23467715 | CCTGGGACAGAAGAG[A/G/T]CAGAAGATGTCAAAT | 23062 |
rs200739276 | snp | A/C | 0.0029955 | 0.0385847 | intron-variant | GGA2 | GRCh38.p7 | 16:23480576 | AGAATATGTTTAGGA[A/C]CCATTTCTTTTCTGG | 23062 |
rs200755753 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497110 | ATCCTGCCTCAAAAA[A/C]AAAAAAAAAAAACAA | 23062 |
rs200759772 | snp | C/T | 0.0140405 | 0.0826022 | intron-variant | GGA2 | GRCh38.p7 | 16:23480608 | AATTACAGGCTGCCC[C/T]AAGGCAGAGAAGGCA | 23062 |
rs200764317 | snp | A/G | 1.65658e-05 | 0.00287795 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23495754 | GACCAATCCTGTTCC[A/G]ACATGCTTGGGTCTG | 23062 |
rs200785119 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473330 | TTTTACTTTTCTAGT[C/T]TTTTTTTTTTTTTTT | 23062 |
rs200809926 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483995 | ACCAGGAAGACATTA[A/C]AAAAAAAAAAAGGCC | 23062 |
rs200839095 | snp | A/G | 3.29598e-05 | 0.00405941 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23474943 | CAAACACTTGAGCCA[A/G]AGGTGTATTCTGTGA | 23062 |
rs200869966 | snp | C/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499145 | ACTGACGGGCACCAC[C/T]TTTTTTTTTTTTTTT | 23062 |
rs200883820 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501341 | GTTTGGAGAAATCAT[-/G]GTCTGTGGAGTGTGG | 23062 |
rs200992596 | snp | A/C | 4.94499e-05 | 0.00497217 | missense | GGA2 | GRCh38.p7 | 16:23486135 | CCTCTTGGACACCTT[A/C]TCCGATTTTTCTTGT | 23062 |
rs201074795 | in-del | -/CT | 0.0584853 | 0.160693 | intron-variant | GGA2 | GRCh38.p7 | 16:23470740 | AGTGACAGAGCGAGA[-/CT]CTGTCTCAAACAAAC | 23062 |
rs201102052 | snp | C/G | 0.000230688 | 0.0107374 | missense | GGA2 | GRCh38.p7 | 16:23486051 | CGGGGCCTGCCCTGG[C/G]CTGCGGTACATGCTC | 23062 |
rs201180104 | snp | A/T | 0.000165415 | 0.00909286 | intron-variant | GGA2 | GRCh38.p7 | 16:23479747 | CTGTGCCTGCTCCCC[A/T]CAAGCACCTGCCCTC | 23062 |
rs201289390 | in-del | -/A | 0.00954252 | 0.068412 | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463246 | GGGAACTGCTACCCC[-/A]GAGTTTTAACATGCA | 23062 |
rs201297457 | snp | A/C | 1.69055e-05 | 0.00290731 | intron-variant | GGA2 | GRCh38.p7 | 16:23478516 | CCTGTCAAATCAGGA[A/C]TGGCTAAAATAAGAC | 23062 |
rs201313210 | snp | C/G | 0.00199792 | 0.0315431 | missense | GGA2 | GRCh38.p7 | 16:23491722 | GAATCTTGATGTCTT[C/G]CGGAAACCAGACTGT | 23062 |
rs201322546 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23483625 | GGCACAGACAGGCTG[G/T]GGTTTCTTTTTGATT | 23062 |
rs201425928 | snp | G/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501089 | TCTGGCTATTTTTGA[G/T]AAGCCAATACACCCA | 23062 |
rs201431736 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509308 | CTGACCTACTTGTTC[A/C]CGGAGTGCTCCACAT | 23062 |
rs201437666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23481645 | AGGTGTGGTGGTGCG[C/T]AACTGTAGTCCCAGC | 23062 |
rs201439823 | snp | A/G | 6.62142e-05 | 0.0057535 | missense | GGA2 | GRCh38.p7 | 16:23470099 | TGCCCAGGGGCTCCC[A/G]TCTGGGAGAAGTGGA | 23062 |
rs201482337 | snp | A/T | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511975 | TATTTTGCATTGGTA[A/T]CAACTTAACAGAGTT | 23062 |
rs201544801 | in-del | -/T | 0.0136621 | 0.0815132 | intron-variant | GGA2 | GRCh38.p7 | 16:23480602 | CTGGGAATTACAGGC[-/T]TGCCCCAAGGCAGAG | 23062 |
rs201587696 | snp | C/G | 0.00031969 | 0.0126389 | missense | GGA2 | GRCh38.p7 | 16:23467609 | GCTGCGCCCAAGACA[C/G]CCAGGTCTGGGAAGT | 23062 |
rs201625518 | in-del | -/GT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509775 | CACACACACACACAC[-/GT]GTGTGTGTGTGTTTA | 23062 |
rs201630631 | snp | A/C/T | 3.39311e-05 | 0.00411879 | intron-variant | GGA2 | GRCh38.p7 | 16:23480606 | GGAATTACAGGCTGC[A/C/T]CCAAGGCAGAGAAGG | 23062 |
rs201654362 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471917 | CCATCTCTAAAAAAA[-/T]TTAAAAAAAAATTAA | 23062 |
rs201728267 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497111 | TCCTGCCTCAAAAAC[A/C]AAAAAAAAAAACAAC | 23062 |
rs201875963 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490739 | GACTCTGTCTCAAAA[A/G]AAAAAAAAAAAAAAG | 23062 |
rs201952580 | snp | C/T | 0.00141891 | 0.0265978 | intron-variant | GGA2 | GRCh38.p7 | 16:23495783 | TGTGGCTTTGTCTGT[C/T]AAATAAATAATAAAG | 23062 |
rs201963634 | snp | C/G | 0.000399281 | 0.0141238 | missense | GGA2 | GRCh38.p7 | 16:23491773 | TGACTCTTCCTTTAA[C/G]TTTTCCTGTGGCCCA | 23062 |
rs201987403 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470768 | AAACAAACAAACAAA[A/C]AACAAAAAGCCACAC | 23062 |
rs202075370 | snp | A/G | 8.28727e-05 | 0.00643657 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23482924 | GAAAGAAAACTTACC[A/G]AGTGCATCATCGTCA | 23062 |
rs202099715 | snp | A/G | 1.78828e-05 | 0.00299017 | intron-variant | GGA2 | GRCh38.p7 | 16:23478358 | CACTCCCCTTGCCCA[A/G]AAGACTCACAGAGGG | 23062 |
rs202121859 | snp | C/T | | | downstream-variant-500B | GGA2 | GRCh38.p7 | 16:23463530 | TTATCTTAAAAAAGA[C/T]GACACTGAGCATAAA | 23062 |
rs202139118 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | GGA2 | GRCh38.p7 | 16:23506884 | GTCCTTCCTCTCTGT[A/G]AGGCCAGGTCCCCCT | 23062 |
rs202142731 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475943 | TCAGGAAAAAAAAAA[A/G]AAAAAAACAAAAGCA | 23062 |
rs202161732 | snp | A/G | 0.000164747 | 0.0090745 | missense | GGA2 | GRCh38.p7 | 16:23488691 | TCCACTGGTAGTTTA[A/G]GGTCTTGTTTTATAA | 23062 |
rs202188100 | snp | C/T | 5.05029e-05 | 0.00502483 | missense | GGA2 | GRCh38.p7 | 16:23470135 | ATTCTGAATCCATTC[C/T]GGTCATACACAATGA | 23062 |
rs367550356 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490627 | GTAATCCCAGCTACT[C/T]GAGAAGCTGAGGCAC | 23062 |
rs367601426 | snp | G/T | 1.64746e-05 | 0.00287002 | intron-variant | GGA2 | GRCh38.p7 | 16:23486814 | AGTGAACAGGAAGAG[G/T]AGGTGAGACCACAAC | 23062 |
rs367624626 | snp | C/T | 0.000116249 | 0.00762306 | intron-variant | GGA2 | GRCh38.p7 | 16:23479715 | GGAACCAGCTCACTC[C/T]CCTACTCGCACCCAT | 23062 |
rs367645509 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23497981 | TCCACAGAAATTTTT[A/T]AAAAAAATTAGTCAG | 23062 |
rs367649613 | snp | A/C | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465091 | ATCATGAATTTGCTT[A/C]TCCCCAGAGGAAAAG | 23062 |
rs367713045 | snp | A/C/G | 3.29713e-05 | 0.00406015 | missense | GGA2 | GRCh38.p7 | 16:23493367 | GTACTCACCTTTGGG[A/C/G]ACAACACTTTGATCA | 23062 |
rs367720663 | snp | A/C/T | 3.33824e-05 | 0.00408538 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470044 | GACAGGCTGGGGAGC[A/C/T]GTGCTCATCATGGTC | 23062 |
rs367779965 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481648 | TGTGGTGGTGCGCAA[C/T]TGTAGTCCCAGCTAC | 23062 |
rs367802093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23496116 | GACTAGCCTGACCAA[C/T]ATGATGAAACCCCAT | 23062 |
rs367808095 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472920 | GCACCTGTGTCCCAG[A/C]TACTCGGGAGGCTGA | 23062 |
rs367831044 | snp | A/G | 3.36061e-05 | 0.00409901 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23483002 | ACACCTCTCATACAC[A/G]ACCTGAAAGAGCAGA | 23062 |
rs368020787 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23493387 | CACTTTGATCAGTTC[A/G]TTCAGGAAACGAAAT | 23062 |
rs368074688 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495282 | ACGTGTCTATAGTCT[A/G]TCAGTAACATTCAGA | 23062 |
rs368074817 | snp | C/T | 0.0432848 | 0.140602 | intron-variant | GGA2 | GRCh38.p7 | 16:23510274 | GCGGGAAGCGAGGCC[C/T]CACGTGCGGCGCAGC | 23062 |
rs368082908 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472339 | GCTGGGACTACAGGC[A/G]CCCACCACCACGCCT | 23062 |
rs368129290 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | GGA2 | GRCh38.p7 | 16:23494432 | AAAAGAAACTAACCC[A/G]AGTGGCTGAGCATGC | 23062 |
rs368162407 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509114 | TATGGCTGCAAGTGA[C/T]GCCTTTAACAGGCTT | 23062 |
rs368382698 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503025 | CTGAATCCTCATCTT[C/T]CCTTGGGTATGGCCA | 23062 |
rs368386562 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478638 | TTGGGGCAAGAGGGG[A/G]AAGAAAGGGCAAGAT | 23062 |
rs368481420 | snp | A/G | 3.29468e-05 | 0.00405861 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486758 | AGCCTGAAGGTCCTC[A/G]GGGTGGTTGCTCTTT | 23062 |
rs368528042 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23473099 | AGTGCATATATATAT[-/AA]GTTCATTAAAAATCA | 23062 |
rs368632104 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473077 | GATTACAGTACCTCT[A/G]CTTAATAGTGCATAT | 23062 |
rs368638066 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23490143 | AGGAAAGTGAAGACC[C/T]ACAGCTGAGAGAACA | 23062 |
rs368677863 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468598 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTAGGACTA | 23062 |
rs368710191 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23477967 | TCTTGGCCAGGCAGA[C/T]GGATCACCTGAGGTC | 23062 |
rs368831806 | snp | C/G/T | 3.29458e-05 | 0.00405857 | missense, synonymous-codon | GGA2 | GRCh38.p7 | 16:23488666 | GGGAGATGGTGGGGG[C/G/T]AAGATTTTATCCACT | 23062 |
rs368996018 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GGA2 | GRCh38.p7 | 16:23497805 | TAGTCACATGTACTT[A/G]GACTCGCTGAGCCTC | 23062 |
rs369012215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23479209 | TATGTGCTTCCTGAG[A/G]GGACCAGCTCACTCC | 23062 |
rs369054068 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503838 | TGTAATCCCAGCATT[C/T]TGGGAGGCCAAGGTG | 23062 |
rs369089418 | in-del | -/TCCTTC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468121 | TTTCTTTTTCTCTTC[-/TCCTTC]CTTCCTTTCCTCCTT | 23062 |
rs369126237 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497360 | GCTCCTGCAGAAAAC[C/T]TCCTCCCGCTGCGCC | 23062 |
rs369130729 | snp | A/C | 1.8027e-05 | 0.00300219 | intron-variant | GGA2 | GRCh38.p7 | 16:23478320 | CCCATGAGAAGGAAC[A/C]GCACTCAGGAGCCAC | 23062 |
rs369262019 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474512 | ACAGGCATGCACCAC[C/G]ATGTCCAGCTAATGT | 23062 |
rs369266260 | snp | A/C/G | 1.66885e-05 | 0.00288859 | missense | GGA2 | GRCh38.p7 | 16:23478399 | GCTGTGCTGAGAGGA[A/C/G]GTCCAGCAAATTCCT | 23062 |
rs369281290 | snp | C/T | 1.64974e-05 | 0.00287201 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494346 | TGCGGAGACTGGATC[C/T]TGTGGGCCAGTAGCC | 23062 |
rs369283257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GGA2 | GRCh38.p7 | 16:23485164 | GCAACCGCATTTGGA[C/T]GAAGCATCCAAATAA | 23062 |
rs369399289 | snp | G/T | 6.31373e-05 | 0.00561824 | intron-variant | GGA2 | GRCh38.p7 | 16:23493509 | AGCCAGTGGTCCCAG[G/T]CTCCCCTCCAGGCTG | 23062 |
rs369401636 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487744 | GGAAAGCGGAGAAAG[A/G]TGGCCTGGAACCTAG | 23062 |
rs369477294 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23496684 | AATTAAGACCAGGCG[C/G]GATGGCTCACGCCTG | 23062 |
rs369479163 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | GGA2 | GRCh38.p7 | 16:23485981 | AACCCACTTTAGTAA[A/G]CATGTGCAGCCCCCT | 23062 |
rs369621603 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23473578 | AGTGATCTGCCCACC[A/T]TGGCCTCCCAAAGTG | 23062 |
rs369710113 | snp | C/T | 8.31871e-05 | 0.00644877 | missense | GGA2 | GRCh38.p7 | 16:23479873 | TCTTCATGCAGCCTG[C/T]TGGATTCTGAAAGAC | 23062 |
rs369774199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487892 | ACGCAGCGTGTAGCC[G/T]TCCAACACTCCATGA | 23062 |
rs369780983 | snp | A/G | 1.67223e-05 | 0.00289151 | intron-variant | GGA2 | GRCh38.p7 | 16:23488741 | CAAAGTTAAGACACC[A/G]ATATGGTACCCAGAA | 23062 |
rs369812669 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504252 | GGCTGGCCCAGCTCC[A/C]CAGCCTGGATGTGTT | 23062 |
rs369832264 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479687 | CTCAGCAGCAGGCAT[A/G]TGCTCCGCGAAGGGA | 23062 |
rs369898885 | in-del | -/CA | | | intron-variant | GGA2 | GRCh38.p7 | 16:23509761 | ATATATATATATACG[-/CA]CACACACACACACGT | 23062 |
rs369906029 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492131 | TTCCTGGCACAGAAC[C/T]TCAAAAATCCTTGGA | 23062 |
rs369926015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478194 | ACAGAGTGAGACCCC[A/G]TCTCAAAAAAAAAAA | 23062 |
rs369932812 | snp | C/T | 4.94173e-05 | 0.00497053 | missense | GGA2 | GRCh38.p7 | 16:23488635 | CATCAGCATCAAAGA[C/T]GGAGCTCTTGGGCCA | 23062 |
rs370003192 | snp | C/T | 4.95864e-05 | 0.00497903 | intron-variant | GGA2 | GRCh38.p7 | 16:23480796 | AGGGAAGACTCAGAA[C/T]CCCCTGGTTTGGCAA | 23062 |
rs370024823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23504656 | ACCGCCGTAGGTCTG[C/T]TTGACACCAATCTGC | 23062 |
rs370050570 | snp | A/C | 4.94181e-05 | 0.00497057 | missense | GGA2 | GRCh38.p7 | 16:23491730 | ATGTCTTCCGGAAAC[A/C]AGACTGTCCAACTGA | 23062 |
rs370127259 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507258 | CGTTCCTGAAAAACA[G/T]GAAGATCTAGCAACT | 23062 |
rs370171848 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23482744 | TGCTGATTTCTTACT[A/G]AAGCCTGGATCCTGC | 23062 |
rs370195821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23498132 | CAAAATACAAATAAT[C/T]AGCTGGGCGTGGCAG | 23062 |
rs370216768 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23512166 | TGAGGCAGGTTTACT[A/G]AGGGGACTTACGGGG | 23062 |
rs370261106 | in-del | -/T | 0.388398 | 0.208197 | intron-variant | GGA2 | GRCh38.p7 | 16:23475190 | TAGATGTTATATGCC[-/T]TTTTTTTTTTTTTTT | 23062 |
rs370266306 | snp | G/T | 0.000106313 | 0.00729008 | missense | GGA2 | GRCh38.p7 | 16:23467627 | AGGTCTGGGAAGTCT[G/T]TCACTTCTCCTACTT | 23062 |
rs370279614 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481449 | AAACTGAGACCGAGA[G/T]AACTGTCAATTCAGA | 23062 |
rs370311370 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489349 | AAGCAGTCCTCTCAC[C/T]TTGGCCTCCCAAGTA | 23062 |
rs370318665 | snp | C/G/T | 0.000347939 | 0.0131852 | intron-variant | GGA2 | GRCh38.p7 | 16:23479713 | AGGGAACCAGCTCAC[C/G/T]CCCCTACTCGCACCC | 23062 |
rs370349546 | in-del | -/AC | 0.0146672 | 0.084371 | intron-variant | GGA2 | GRCh38.p7 | 16:23475153 | AACAAGGAAAAAATA[-/AC]ACACACACACACACA | 23062 |
rs370398188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500721 | TAACATCACGCAGGC[A/G]GAGGTGGCAGTAGCG | 23062 |
rs370416839 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473031 | GCGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 23062 |
rs370494973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499365 | TGGCCAGGCTAGTCT[C/T]GAACTACTGACCTCG | 23062 |
rs370615038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480055 | CACACAAGCTCAGCT[A/G]GCATCCAAGACAAGA | 23062 |
rs370626280 | in-del | -/GT/GTGT | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511016 | AGACTGGGTTTCACC[-/GT/GTGT]GTGTGTGTGTGTGTG | 23062 |
rs370686221 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478225 | AAAAAGAAAAAAAGA[A/C]AAAAAAAAAAAAAAG | 23062 |
rs370749380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23498975 | TTCAGCATGTGACTG[C/G]ACCTGGAGGGAGAGA | 23062 |
rs370777047 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478216 | AAAAAAAAAAAAAAG[-/A]AAAAAAGACAAAAAA | 23062 |
rs370781819 | snp | A/G | 1.64746e-05 | 0.00287002 | stop-gained | GGA2 | GRCh38.p7 | 16:23486098 | CCTTCACATGGCTTC[A/G]CACTTCCTCCACCGC | 23062 |
rs370865571 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506334 | TCTGACTTAACCCAT[A/C]GTTCACTTCATCTTC | 23062 |
rs370894795 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | GGA2 | GRCh38.p7 | 16:23489446 | GGGTCTCGCTATGTT[A/G]CCCAGGCTGGTCTCA | 23062 |
rs371026520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23476232 | ACCCTGCCCGAGTGG[C/T]TGAAAAAAAGAAGAC | 23062 |
rs371041635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23482004 | GGGGATCGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23062 |
rs371066023 | snp | C/T | 1.79858e-05 | 0.00299876 | intron-variant | GGA2 | GRCh38.p7 | 16:23469947 | CAGAAAAGAACCTGG[C/T]ACTCAAAAACGACAG | 23062 |
rs371201012 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507499 | CAGACATGGTGGCTA[A/G]TGCCTGTAATCCCAG | 23062 |
rs371228612 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495322 | AGCATTAGTGTTTTA[C/T]AACAGTATTTAAAAT | 23062 |
rs371236805 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472347 | TACAGGCGCCCACCA[C/T]CACGCCTGGCTAATT | 23062 |
rs371261820 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486570 | AGGGAGACTATGGCT[-/G]GTTCCCCAGAGTTCA | 23062 |
rs371308868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486247 | CTATTGAGAGAGCTC[A/G]CTCAGGGGCATCACC | 23062 |
rs371310485 | snp | A/C/T | 1.65718e-05 | 0.00287848 | intron-variant | GGA2 | GRCh38.p7 | 16:23493317 | GAGTTTGACAGTGGG[A/C/T]GTAGGTGCGACACAG | 23062 |
rs371311773 | snp | C/T | 6.60371e-05 | 0.0057458 | intron-variant | GGA2 | GRCh38.p7 | 16:23493342 | ACACAGTCAGCAGAG[C/T]CAAGCCCAGGTACTC | 23062 |
rs371328012 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465010 | ACGAAATGGGTCAAC[A/G]GGACCCCCGAAGAGT | 23062 |
rs371504605 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465270 | GATTATAGGCGTGAG[A/C]CACTGTGCACAGCCA | 23062 |
rs371573969 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23504643 | CCAGGCCACAGCAAC[A/C]GCCGTAGGTCTGTTT | 23062 |
rs371676806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23490456 | AAATAAATCCACAGC[C/T]GGGAGCGGTGGCTCA | 23062 |
rs371684249 | snp | A/C | 4.96882e-05 | 0.00498414 | intron-variant | GGA2 | GRCh38.p7 | 16:23479737 | CGCACCCATCCTGTG[A/C]CTGCTCCCCACAAGC | 23062 |
rs371717799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500184 | GCTGAGGTGGGGTGC[A/G]GGCTGCTAGTGGGGA | 23062 |
rs371749122 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | GGA2 | GRCh38.p7 | 16:23486778 | GGTTGCTCTTTAGAA[A/G]CCTTGTCAGAAGCTG | 23062 |
rs371782021 | snp | A/G | 6.90775e-05 | 0.00587656 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23470161 | AATGAGAGGCGGCAG[A/G]CTGCCTGGTATAAAG | 23062 |
rs371785192 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23510312 | CCGAAGGCCTGCCAG[A/G]CTACTCACTGAGCCA | 23062 |
rs371907730 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | GGA2 | GRCh38.p7 | 16:23495635 | TCTTGAGAGACAAAG[G/T]CCTACACTCAGTGTG | 23062 |
rs371984702 | in-del | -/AC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475154 | AACAAGGAAAAAATA[-/AC]ACACACACACACACA | 23062 |
rs372013915 | snp | C/T | 0.000153988 | 0.00877328 | missense | GGA2 | GRCh38.p7 | 16:23493388 | ACTTTGATCAGTTCG[C/T]TCAGGAAACGAAATT | 23062 |
rs372143718 | snp | G/T | 0.000131774 | 0.00811601 | intron-variant | GGA2 | GRCh38.p7 | 16:23488595 | GACACCATGTAGGTC[G/T]GTTTCCTTACCTTGG | 23062 |
rs372190298 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | GGA2 | GRCh38.p7 | 16:23496671 | TAAAATTTTAAAAAA[C/T]TAAGACCAGGCGCGA | 23062 |
rs372229464 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494303 | GCAAGCCAAACTCAC[C/T]GTTAAGGCATAAAGA | 23062 |
rs372233719 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495501 | AGTCTCTCACTCTGT[C/T]ACCCAGGCAGGTCTC | 23062 |
rs372255357 | snp | A/G | 8.23934e-05 | 0.00641794 | missense | GGA2 | GRCh38.p7 | 16:23474948 | ACTTGAGCCAGAGGT[A/G]TATTCTGTGAAGATG | 23062 |
rs372305424 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492358 | GGAGGTGGTGGGGCG[A/G]GCAGGGGGGTGTGAA | 23062 |
rs372390577 | snp | C/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501792 | GGATTTTCATCGAGA[C/G]GAAACATCTTCAAGT | 23062 |
rs372403659 | snp | C/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467118 | TACTCTCTGCCCCAA[C/G]ACTAACCAGGTCCCT | 23062 |
rs372500251 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497189 | TCTCTGATGAGAAAC[C/T]GTACTGGTTCTGACA | 23062 |
rs372562760 | snp | A/G | 1.65053e-05 | 0.0028727 | missense, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23494358 | ATCTTGTGGGCCAGT[A/G]GCCAGGGCGCATGTG | 23062 |
rs372657289 | snp | A/G | 3.1126e-05 | 0.00394487 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467552 | AGCAAAAGTAACGCC[A/G]GCCTAAGCTTGAAAT | 23062 |
rs372659406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23479367 | TCACTCCCCTACTCA[C/T]ACCCATCCCGATTCC | 23062 |
rs372689483 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481310 | CCCAGGAGACGGAGG[C/T]TGCAGCGAGCTGAGA | 23062 |
rs372793328 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | GGA2 | GRCh38.p7 | 16:23483049 | ACGCCCAGGCACCCC[A/G]TAACGCCCCCCTCCA | 23062 |
rs372815363 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468121 | TTTCTTTTTCTCTTC[-/T]CCTTCCTTCCTTTCC | 23062 |
rs372821138 | snp | C/T | 4.95872e-05 | 0.00497907 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23482954 | ATCAGTGGTGTCACT[C/T]GCCAACCGGAACAGC | 23062 |
rs372992706 | in-del | -/AT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471382 | TGAGGGGGGAAAACT[-/AT]GTAAGACTGACCAAT | 23062 |
rs373089495 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473319 | GGTATAGATGATTTT[A/T]CTTTTCTAGTCTTTT | 23062 |
rs373113452 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504229 | GCAGAAACAAAAATT[A/C]AGTCATAGGCTGGCC | 23062 |
rs373172365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487790 | TCTAACAACAGGGAC[A/C]TGATGGCCACAGAGT | 23062 |
rs373214904 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23496827 | GCTGGGCGTGGTGGA[A/G]TGTTCCTGTAATCCC | 23062 |
rs373267126 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23504561 | TAATCCCAGCCTGCA[A/C]AAACTATTTCAGAAG | 23062 |
rs373275019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23471597 | TAATATCAAAATATA[C/T]ATTACTAAAATATAG | 23062 |
rs373294083 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GGA2 | GRCh38.p7 | 16:23498545 | CAAGCCTGGGCAACA[C/T]AGTGAGGCCCCATCT | 23062 |
rs373320474 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | GGA2 | GRCh38.p7 | 16:23491701 | TCAGCATCTGATAAG[C/T]GTCTCGAATCTTGAT | 23062 |
rs373329210 | snp | A/C | 1.85057e-05 | 0.00304179 | intron-variant | GGA2 | GRCh38.p7 | 16:23467728 | AGACAGAAGATGTCA[A/C]ATCAGTGGAGAGCAA | 23062 |
rs373357055 | snp | C/G | | | missense | GGA2 | GRCh38.p7 | 16:23493364 | CAGGTACTCACCTTT[C/G]GGGACAACACTTTGA | 23062 |
rs373359035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GGA2 | GRCh38.p7 | 16:23470241 | CTGGAAAGAGATGTA[C/T]ATGTTATCCCCAGAT | 23062 |
rs373374099 | in-del | -/A | 0.198634 | 0.244666 | intron-variant | GGA2 | GRCh38.p7 | 16:23478037 | TCTCTACTAAAAATT[-/A]AAAAAAAAAAAATTA | 23062 |
rs373393695 | snp | A/G | 0.00150633 | 0.0274025 | intron-variant | GGA2 | GRCh38.p7 | 16:23475078 | TACAAAGAAATAAAA[A/G]ATATCAAAGACTAGC | 23062 |
rs373428849 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487332 | TTACTTCTCCCAGGG[G/T]ATGTCTGGCTAAGTC | 23062 |
rs373438484 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488511 | AGAACCCATGTAACC[C/T]GCCCCCCTCCATACT | 23062 |
rs373454551 | snp | A/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23480384 | GCTCCTGTATGCAAG[A/C]ATTTATGAGAATTCA | 23062 |
rs373473219 | snp | A/G | 0.000230593 | 0.0107351 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23491747 | GACTGTCCAACTGAA[A/G]AGTATTTCAATGACT | 23062 |
rs373479355 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23498383 | AGTGAGCTATGATTG[C/T]GCAACTGCACTCCAG | 23062 |
rs373513794 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505633 | CTCCTCAATTCCAGG[C/T]CCCCCATTCACCCTC | 23062 |
rs373542228 | snp | A/G | | | missense | GGA2 | GRCh38.p7 | 16:23479822 | TCCCCATCTGCGCAG[A/G]TCCATTGTCCACCTC | 23062 |
rs373557447 | snp | A/C | 0.000183176 | 0.00956841 | missense | GGA2 | GRCh38.p7 | 16:23478434 | GCAGAAGGGTTCTGA[A/C]CACCACCGCCTGGCA | 23062 |
rs373588905 | snp | A/C | 0.000155875 | 0.00882685 | intron-variant | GGA2 | GRCh38.p7 | 16:23479929 | AGTCAGTTGGACATG[A/C]GAGCAAAGTCTCCAC | 23062 |
rs373665865 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493166 | AGGGAAATGTGAAAA[G/T]GCTAACAGTGAGGGG | 23062 |
rs373742002 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487981 | CAAAGGGCTCCCCAC[C/T]CACAGGCACCACAGT | 23062 |
rs373744085 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | GGA2 | GRCh38.p7 | 16:23481511 | TGTGTGGTGGTTCAC[G/T]CCTGTAATCCCAGCA | 23062 |
rs373763154 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23464600 | GCAATGTAAGTGCAG[A/G]GAGGACATGATGTGG | 23062 |
rs373849069 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488938 | ACTATGTCAGAGAAG[A/G]GCCAGTCCTGAAGGC | 23062 |
rs373857010 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23495268 | CTTTTAATTAGGTAA[C/T]GTGTCTATAGTCTAT | 23062 |
rs373860982 | snp | A/G | 9.01185e-05 | 0.00671201 | intron-variant | GGA2 | GRCh38.p7 | 16:23478321 | CCATGAGAAGGAACC[A/G]CACTCAGGAGCCACA | 23062 |
rs373921632 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | GGA2 | GRCh38.p7 | 16:23485982 | ACCCACTTTAGTAAA[C/T]ATGTGCAGCCCCCTG | 23062 |
rs373930514 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497378 | CTCCCGCTGCGCCAA[C/T]CCCACTGCTTCTCCC | 23062 |
rs373951620 | in-del | -/AAGTGAGACAGC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491053 | ACAAATATTTGGTGT[-/AAGTGAGACAGC]AAGTGAGACAGAGAC | 23062 |
rs374112004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476832 | AAAACAAAAACAAAC[A/G]GCAAAAACCTCATGT | 23062 |
rs374131213 | snp | A/C/T | 0.0001322 | 0.00812919 | intron-variant | GGA2 | GRCh38.p7 | 16:23480797 | GGGAAGACTCAGAAC[A/C/T]CCCTGGTTTGGCAAC | 23062 |
rs374219182 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489708 | AGTGTGAGCTACCAA[C/G]AGAATACAGAATTTC | 23062 |
rs374339577 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23476340 | TATCAGGAACATGGG[C/T]ACTTTCAGGCTGTTT | 23062 |
rs374379857 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474618 | TGCCTTGGCCTCCCA[A/G]TTTTTTTCTTCCCCC | 23062 |
rs374434818 | snp | A/G | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499928 | CTCCCGCATCACGAT[A/G]GGAACAGGGCATGTG | 23062 |
rs374479634 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23480679 | TCCCAATGAGCTGGT[C/T]ACTCTGTTTCCAAAG | 23062 |
rs374479666 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506904 | CAGGTCCCCCTTTTT[G/T]CTCTGGCTCTGAGCT | 23062 |
rs374479875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501370 | GGATGACAGCCAGAA[A/T]CCCAAGGACATTGCA | 23062 |
rs374701699 | in-del | -/TGGTCTCGAACTCCTGGG | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511081 | ACCATGTTGCCCGGG[-/TGGTCTCGAACTCCTGGG]CTACAAGATCCTCTT | 23062 |
rs374719399 | in-del | -/TTT | | | intron-variant | GGA2 | GRCh38.p7 | 16:23486981 | TGGTTTTCTTTTCTG[-/TTT]TTGTTTTTTTTTTTT | 23062 |
rs374742540 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23471084 | GACCTCAGGTGATCC[A/G]CCCACCTTGACCTCC | 23062 |
rs375172271 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23468472 | TGAGCCACTGCACCT[A/G]GCCGACTTTATTTTT | 23062 |
rs375192353 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23497293 | GCCCGAGTGTCCACT[C/G]TGTTCCTCTCAGTGC | 23062 |
rs375212050 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478240 | CAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGATG | 23062 |
rs375256232 | snp | A/G | 0.000132332 | 0.00813317 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23482936 | ACCGAGTGCATCATC[A/G]TCATCAGTGGTGTCA | 23062 |
rs375263345 | snp | A/G | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511104 | AACTCCTGGGCTACA[A/G]GATCCTCTTACCTCG | 23062 |
rs375311401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23491237 | GCTGGAGTCCAGAAG[G/T]TCGAGGCTACAGTGA | 23062 |
rs375334128 | snp | C/T | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465801 | CAAAAATTAGCTGGG[C/T]GTGCTGGCTCACGCC | 23062 |
rs375373475 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23463690 | GCTTTAAAACAAACT[C/G]GGGTCAGGACATGGT | 23062 |
rs375426932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487645 | ATAATGAGGGCTGGT[A/G]ACACAGGATTGTTTC | 23062 |
rs375497544 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23492506 | CCTCAGATGAAAACA[C/T]TGAAACAAGGAAGCT | 23062 |
rs375528212 | snp | A/G | 0.000183347 | 0.00957287 | intron-variant | GGA2 | GRCh38.p7 | 16:23488736 | ATTTACAAAGTTAAG[A/G]CACCGATATGGTACC | 23062 |
rs375715093 | snp | C/T | 6.58903e-05 | 0.00573941 | missense | GGA2 | GRCh38.p7 | 16:23491716 | CGTCTCGAATCTTGA[C/T]GTCTTCCGGAAACCA | 23062 |
rs375715462 | snp | C/T | 1.66582e-05 | 0.00288597 | missense | GGA2 | GRCh38.p7 | 16:23482992 | GCAGCTTTTCACACC[C/T]CTCATACACGACCTG | 23062 |
rs375739252 | in-del | -/AAAG/G | 0.00153143 | 0.0276317 | intron-variant | GGA2 | GRCh38.p7 | 16:23474876 | CAGGGAAAAAAAAAA[-/AAAG/G]AAAGGTGGGGAGTGA | 23062 |
rs375940202 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | GGA2 | GRCh38.p7 | 16:23493349 | CAGCAGAGCCAAGCC[C/T]AGGTACTCACCTTTG | 23062 |
rs375948844 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489081 | GAGTGTATGTGACAG[A/G]GAACAACAGTCCATC | 23062 |
rs376003356 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23473390 | TGCTCAGACTGAAGC[A/G]CAGTGGCACGATCTC | 23062 |
rs376010071 | snp | C/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503449 | TGTAAGATATAGTTA[C/T]TTAAATGTTTCCAAA | 23062 |
rs376018575 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506993 | GGGGCAGTTCCCCAA[A/T]GGAACATCAACATGA | 23062 |
rs376095120 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465686 | TGGCTCACGCCTGTA[A/G]TCCCAGCACTCTGGG | 23062 |
rs376129938 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | GGA2 | GRCh38.p7 | 16:23492729 | TGGAATATGGGGCGG[-/T]GGGGGTCATAGGAAC | 23062 |
rs376199237 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23506136 | CCCATCTTAAAGATA[A/C]AGCTGCCTTGTTTGC | 23062 |
rs376276782 | snp | G/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500367 | TTGCTTGAGCACCAA[G/T]GCCAGCCCCAGGTAG | 23062 |
rs376283504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23476399 | GGCAAAGGGACAGGA[A/T]CTATGAAAATGTTGT | 23062 |
rs376345637 | snp | C/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508763 | CACTTGCCCTCTCCA[C/G]TGCCAACCAGCTGCC | 23062 |
rs376410677 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23472320 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 23062 |
rs376437354 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23467089 | TCTTTCTTGGAAGAG[A/G]GTGCCCAAGTAGATA | 23062 |
rs376533678 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23481317 | GACGGAGGTTGCAGC[A/G]AGCTGAGATCGCACC | 23062 |
rs376541644 | snp | A/C/T | 0.000639837 | 0.0178751 | intron-variant | GGA2 | GRCh38.p7 | 16:23483053 | CCAGGCACCCCATAA[A/C/T]GCCCCCCTCCAGGGC | 23062 |
rs376579898 | snp | C/T | 0.000107766 | 0.00733973 | intron-variant | GGA2 | GRCh38.p7 | 16:23478348 | CACACTCTCCCACTC[C/T]CCTTGCCCAGAAGAC | 23062 |
rs376619559 | snp | A/G | 0.000304013 | 0.0123253 | missense | GGA2 | GRCh38.p7 | 16:23475050 | GGGACACTTTTCTGC[A/G]AAACATAATTCCTAC | 23062 |
rs376631291 | snp | C/G | 1.65589e-05 | 0.00287736 | intron-variant | GGA2 | GRCh38.p7 | 16:23479736 | TCGCACCCATCCTGT[C/G]CCTGCTCCCCACAAG | 23062 |
rs376640972 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | GGA2 | GRCh38.p7 | 16:23486782 | GCTCTTTAGAAGCCT[C/T]GTCAGAAGCTGCAGA | 23062 |
rs376664625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23479539 | TCTCCCTGACTTGCT[C/G]AGCAGCAGACACGTG | 23062 |
rs376727129 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23487241 | CACCTCGGCCTCCCA[A/G]AATGCTGGGATTACA | 23062 |
rs376746471 | snp | A/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23474179 | ATTCATCCACTCGTT[A/T]GAATTCTACCTCTTG | 23062 |
rs376848364 | snp | A/C | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503670 | ATGTTGTGTAAAATA[A/C]TTCGTGCCCTGCACT | 23062 |
rs376919279 | snp | C/T | 0.000158335 | 0.0088962 | intron-variant | GGA2 | GRCh38.p7 | 16:23483035 | TTGGTTCATGACACA[C/T]GCCCAGGCACCCCAT | 23062 |
rs376930163 | snp | A/G | 3.31301e-05 | 0.00406989 | intron-variant | GGA2 | GRCh38.p7 | 16:23491804 | GGACCCCAGGTACTG[A/G]AAGTAAAAAGGAAAG | 23062 |
rs377028739 | snp | C/G | 1.66092e-05 | 0.00288172 | intron-variant | GGA2 | GRCh38.p7 | 16:23480613 | CAGGCTGCCCCAAGG[C/G]AGAGAAGGCAAGGAG | 23062 |
rs377047053 | snp | A/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502181 | ATGGTGGGAAGAGAG[A/T]GTGGCATCGGGGCAA | 23062 |
rs377072798 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488224 | CACTCCCCACGGGCT[A/G]TCCTTCTGCACCTTC | 23062 |
rs377128697 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23488072 | TAACGGTTTGGGGAG[C/T]TCATGGTGGATGGAA | 23062 |
rs377173596 | snp | G/T | 9.9633e-05 | 0.00705738 | missense | GGA2 | GRCh38.p7 | 16:23468981 | TGGATGCCGGCTGCA[G/T]CTTCACTCTCATTGA | 23062 |
rs377187680 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23494976 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 23062 |
rs377189957 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23479070 | GGCCAATCTGTGACT[A/G]ATATGCAAGGGGGAC | 23062 |
rs377383705 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | GGA2 | GRCh38.p7 | 16:23497780 | GATAGGGATCTCCAG[C/T]TACACCCATTAGTCA | 23062 |
rs377387731 | snp | G/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23475362 | GTCCGACTAATTTTT[G/T]TATTTTTATTAGAGA | 23062 |
rs377444906 | snp | A/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23493480 | AGACACAGGACCCCC[A/G]GGAGAAGGTGGAAAG | 23062 |
rs377576410 | in-del | -/G | | | intron-variant | GGA2 | GRCh38.p7 | 16:23478215 | AAAAAAAAAAAAAAA[-/G]AAAAAAAGACAAAAA | 23062 |
rs377623556 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | GGA2 | GRCh38.p7 | 16:23493326 | AGTGGGCGTAGGTGC[A/G]ACACAGTCAGCAGAG | 23062 |
rs377654713 | snp | A/G | 1.69502e-05 | 0.00291115 | intron-variant | GGA2 | GRCh38.p7 | 16:23478525 | TCAGGAATGGCTAAA[A/G]TAAGACCAGGGTATG | 23062 |
rs377655661 | snp | A/G | 1.90058e-05 | 0.00308262 | intron-variant | GGA2 | GRCh38.p7 | 16:23495813 | GTTAGAGAGTACATA[A/G]TAGGAAGAAATTTAC | 23062 |
rs377664675 | in-del | -/TC | | | intron-variant | GGA2 | GRCh38.p7 | 16:23507639 | CTCTCTCTCTCTCTC[-/TC]ACACACACAAATTAG | 23062 |
rs377701974 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23470668 | TTTGAGAGGCTGAGG[C/T]ACGAAAATCACTTGA | 23062 |
rs386789814 | in-del | GA/T | | | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503736 | ATTTTCCTATGGGGG[GA/T]AAAAAGATTTATCAT | 23062 |
rs397699913 | in-del | -/CA | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466679 | TGTCTATCTGTACCA[-/CA]GTTTCCCATCTTAGA | 23062 |
rs397727429 | in-del | -/C | | | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23510560 | ACCCCAGGCCCCCCC[-/C]TCCACGCGGGACCGG | 23062 |
rs397767879 | in-del | -/T | | | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499162 | TTTTTTTTTTTTTTT[-/T]GATATGGAGTCTCGC | 23062 |
rs397793157 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506898 | GAGGCCAGGTCCCCC[-/C]TTTTTGCTCTGGCTC | 23062 |
rs397814623 | in-del | -/C | | | intron-variant | GGA2 | GRCh38.p7 | 16:23506897 | TGAGGCCAGGTCCCC[-/C]CTTTTTGCTCTGGCT | 23062 |
rs397855368 | in-del | -/A | | | intron-variant | GGA2 | GRCh38.p7 | 16:23491548 | AAAAAAAAAAAAAAA[-/A]CTCTACCTCAGTGTC | 23062 |
rs397855668 | in-del | -/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23508080 | TTTTTTTTTTTTTTT[-/T]GAGACAGAATCTCGC | 23062 |
rs398042086 | in-del | -/GAAAA | 0.5 | 0 | intron-variant | GGA2 | GRCh38.p7 | 16:23495092 | GGAAAAAAAAAAAAA[-/GAAAA]GAAAAGAAAACAAAA | 23062 |
rs527295816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23479202 | CAGCAGGTATGTGCT[A/T]CCTGAGGGGACCAGC | 23062 |
rs527296050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23486564 | GCCCTTGAGGGAGAC[A/T]ATGGCTGTTCCCCAG | 23062 |
rs527332151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23471740 | TCTGCCTCCCACCCT[C/T]AAAAAGACAATAAAA | 23062 |
rs527448279 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23499865 | AATGAATGAAAGGTA[C/G]GGGTGGGGCCGCTGG | 23062 |
rs527488607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23500306 | GGCCCAAGCTACCGG[A/G]GAGGAGCCAGGAGCC | 23062 |
rs527645595 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23505462 | AAAAGAACAAGGCGG[C/T]TACATCTGCAGTCAT | 23062 |
rs527668695 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23478166 | ATTGTGCCACTGCAC[A/T]CTAGCCTGGGCAACA | 23062 |
rs527674058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23469915 | GATTCTTTCCTTGAC[A/G]CTCGACAGGTAAGTC | 23062 |
rs527709473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23470517 | CCTGTAATCCCAGCA[A/C]TTTAGGAGGCCAAGG | 23062 |
rs527771228 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23503302 | AATATTAGATGAAAC[A/T]TGTTAAAACATTTCA | 23062 |
rs527809514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23504813 | GGGTGCTGAGAAATA[A/G]CACTGCTGCCATGTA | 23062 |
rs528001153 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23477086 | CCTCCTGAGCAGCTG[C/G]GACTACAGTCATGAC | 23062 |
rs528025516 | snp | C/T | 0.00953873 | 0.0683987 | utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23510472 | GCCGCTGTAGCGTCC[C/T]GGCGCTCTCCTCTGC | 23062 |
rs528064767 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23466639 | ATATTTAGTCACCAC[C/T]TCAATCACTGCTAAG | 23062 |
rs528177966 | snp | A/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | GGA2 | GRCh38.p7 | 16:23511014 | TAGAGACTGGGTTTC[A/T]CCGTGTGTGTGTGTG | 23062 |
rs528178509 | in-del | -/TATT | 0.00199481 | 0.0315187 | intron-variant | GGA2 | GRCh38.p7 | 16:23468194 | GTCTATCTATCTATC[-/TATT]TGATAGAGTCTCGCT | 23062 |
rs528216093 | snp | A/G | | | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465265 | GCTGGGATTATAGGC[A/G]TGAGCCACTGTGCAC | 23062 |
rs528251772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23480912 | TCCAGGTTGTGTCAT[C/T]GGACCCTATCAGGCC | 23062 |
rs528265471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23488380 | AGACCCAGGATGCAG[C/T]GTCTGCCTAAGAACC | 23062 |
rs528305878 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | GGA2 | GRCh38.p7 | 16:23473088 | TCTACTTAATAGTGC[-/AT]ATATATATATAAGTT | 23062 |
rs528458672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23502190 | AGAGAGAGTGGCATC[A/G]GGGCAAGGCTGTCAT | 23062 |
rs528621717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23487856 | CAGTTGACAGGCAGA[A/G]CATACCACGCAGAAA | 23062 |
rs528628906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23495581 | GGATTATAGGCATGA[A/G]CCACCGATCCTTGCC | 23062 |
rs528685458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GGA2 | GRCh38.p7 | 16:23472182 | TGTTCTTTGTAGCCC[A/T]GGTTTTTTTTTTTTT | 23062 |
rs528746344 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | GGA2 | GRCh38.p7 | 16:23465760 | AGCCTGGCCAACATG[A/G]TGAAATCCTGTCTCT | 23062 |
rs528780605 | snp | C/T | | | intron-variant | GGA2 | GRCh38.p7 | 16:23489715 | GCTACCAAGAGAATA[C/T]AGAATTTCTGGAGGC | 23062 |
rs528785666 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GGA2 | GRCh38.p7 | 16:23508652 | TTCAATGCTGGGGCT[A/C]CCCACGCTCTCTTTC | 23062 |
rs528820388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | GGA2 | GRCh38.p7 | 16:23501479 | GCAAGATATTACTTC[A/G]ACCTGTGTGCCTTGG | 23062 |