SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs58049 | snp | A/T | 0.482831 | 0.0910472 | intron-variant | G2E3 | GRCh38.p7 | 14:30581009 | AACAACTTTTATTAC[A/T]TGCAGTCAATGCATA | 55632 |
rs142983 | snp | A/G | 0.404384 | 0.196635 | intron-variant | G2E3 | GRCh38.p7 | 14:30606232 | AAAAAAAAATATTGC[A/G]AACAAAAGTATACTG | 55632 |
rs151066 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619335 | TAATATACTCCCCTT[A/G]ACTTAGTATTTAGCA | 55632 |
rs151067 | snp | A/C/G/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619738 | GGGGGGAAATAGGCT[A/C/G/T]ACATATAAACGATCA | 55632 |
rs170662 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30568882 | AATAAAAACACCAGT[A/T]AAGGTAATTACAGAA | 55632 |
rs170663 | snp | A/C | 0.481396 | 0.0946345 | intron-variant | G2E3 | GRCh38.p7 | 14:30580203 | caacaacaaaaaaaa[A/C]caaaaaCAATCCTTT | 55632 |
rs170665 | snp | A/G | 0.484209 | 0.0874434 | intron-variant | G2E3 | GRCh38.p7 | 14:30599139 | aaaagagattaggac[A/G]tagacaacacaccga | 55632 |
rs172946 | snp | C/T | 0.477684 | 0.103247 | intron-variant | G2E3 | GRCh38.p7 | 14:30578403 | TGGTGTTAGGCTGAC[C/T]GGGCTAGGATGAGAC | 55632 |
rs172947 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | G2E3 | GRCh38.p7 | 14:30591755 | ttgcagatgtaatta[A/G]gttaaggatcttgag | 55632 |
rs189068 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616582 | GAAATAAAAGAGAGT[A/T]ATCAATAGCAGCTTT | 55632 |
rs229139 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616655 | TATATTCATATCATA[A/G]ATTTTATTAGGTCAA | 55632 |
rs229140 | snp | C/T | 0.170408 | 0.236992 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616776 | GTATTTATATTGAGG[C/T]TTATGAAGTATCTAT | 55632 |
rs229176 | snp | A/G | 0.488545 | 0.074807 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558061 | GCTGGGCGTGATGGC[A/G]GGCGCCTGTAGTCCC | 55632 |
rs229177 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | G2E3 | GRCh38.p7 | 14:30560458 | TAACACTTAAAAGTT[C/T]AATAGCAGGAAGAAT | 55632 |
rs229178 | snp | A/G | 0.198324 | 0.244601 | intron-variant | G2E3 | GRCh38.p7 | 14:30561664 | ATAAGCAAAAAGCAC[A/G]GCCTGGAGAAGTCTT | 55632 |
rs229179 | snp | A/T | 0.482831 | 0.0910472 | intron-variant | G2E3 | GRCh38.p7 | 14:30563264 | CAACTGTCTTAAGTG[A/T]TCAAACGGAAAAAGA | 55632 |
rs229180 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | G2E3 | GRCh38.p7 | 14:30566740 | ggttcagtgttgact[A/G]caagtggtggaagtg | 55632 |
rs229181 | snp | C/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30568913 | CACCAGACAGTAAGT[C/T]AAAGCCATACGAGGA | 55632 |
rs229182 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | G2E3 | GRCh38.p7 | 14:30569494 | CAATGTATCTGCTAC[C/T]TTATGTGACAGAGCA | 55632 |
rs229183 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30570094 | aaaacccaaacctgt[A/T]agcaaagaatcctat | 55632 |
rs229184 | snp | A/T | 0.482757 | 0.0912364 | intron-variant | G2E3 | GRCh38.p7 | 14:30570171 | agccaaattctcatt[A/T]gaaaccatagagttc | 55632 |
rs229185 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30570218 | cagagagaagtgatt[A/T]acacatacaaaatat | 55632 |
rs229186 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30570233 | aatcttgaaagcagc[A/C/G]agagagaagtgattt | 55632 |
rs229187 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570456 | atgctttataggagt[A/C]caagagggaccggag | 55632 |
rs229188 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570465 | taccaatatatgctt[A/T]ataggagtacaagag | 55632 |
rs229189 | snp | A/C | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30570492 | caagagactatgaga[A/C]accatcaagtatacc | 55632 |
rs229190 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | G2E3 | GRCh38.p7 | 14:30570881 | ataatctgataaagg[A/G]cttagttagatccac | 55632 |
rs229191 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | G2E3 | GRCh38.p7 | 14:30571889 | caaaagtcttgtaat[A/C]gcaaaaacattttta | 55632 |
rs229192 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575892 | atacatgagcatggg[A/G]tgtttttccatttgt | 55632 |
rs229193 | snp | A/C | 0.0858192 | 0.188533 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575905 | attgattcttcctat[A/C]catgagcatgggatg | 55632 |
rs229194 | snp | C/T | 0.482831 | 0.0910472 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575975 | ttgttggtagtttga[C/T]aggaatagcagtgaa | 55632 |
rs229195 | snp | C/T | 0.482459 | 0.0919928 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576390 | ttttgggttttacat[C/T]taagtctttaatcca | 55632 |
rs229196 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | G2E3 | GRCh38.p7 | 14:30579569 | TAAGACACCACAAAA[C/T]GTAGGACACAGATTA | 55632 |
rs229197 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | G2E3 | GRCh38.p7 | 14:30580168 | GTCTATAccgtattt[A/G]tggctgttgcatttg | 55632 |
rs229198 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580345 | gtggtgcatgcctgt[A/T]atcccagctactcgg | 55632 |
rs229200 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | G2E3 | GRCh38.p7 | 14:30581311 | CTTATATACATAAAA[C/T]AAATATAAAATTTGG | 55632 |
rs229201 | snp | A/G | 0.482609 | 0.0916147 | intron-variant | G2E3 | GRCh38.p7 | 14:30582595 | GCTCAAGAGAAAGAG[A/G]ATTATGTAGAATTAG | 55632 |
rs229202 | snp | C/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30604244 | AATAAAAGCGAAAGT[C/T]CTTTGGAAGTAAGAT | 55632 |
rs229229 | snp | A/G | 0.149399 | 0.228871 | intron-variant | G2E3 | GRCh38.p7 | 14:30607874 | ATTTGATATATTTTC[A/G]TCTGTATTTACAGCT | 55632 |
rs229230 | snp | A/G | 0.215146 | 0.258611 | intron-variant | G2E3 | GRCh38.p7 | 14:30608189 | AGGGATTGTAAACAT[A/G]TATTTCTGTTTACCA | 55632 |
rs229231 | snp | A/G | 0.484421 | 0.0868729 | intron-variant | G2E3 | GRCh38.p7 | 14:30608655 | AAACATGTCACATGT[A/G]CAAACACTCATTTAT | 55632 |
rs229232 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | G2E3 | GRCh38.p7 | 14:30609293 | ATTTCCTATTTATTT[A/C]TTGTAATCAGGCTTC | 55632 |
rs229233 | snp | C/T | 0.198634 | 0.244666 | intron-variant | G2E3 | GRCh38.p7 | 14:30609881 | CTAAGACTGACTTAT[C/T]GTCAACCTTTCCTTC | 55632 |
rs229234 | snp | C/G | 0.191147 | 0.242974 | intron-variant | G2E3 | GRCh38.p7 | 14:30610406 | gatcaccggggtcag[C/G]agttcgagaccagcc | 55632 |
rs229235 | snp | A/G | 0.482757 | 0.0912364 | intron-variant | G2E3 | GRCh38.p7 | 14:30610473 | acaaaaaaattagcc[A/G]ggtgtggtggcgcgc | 55632 |
rs229236 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | G2E3 | GRCh38.p7 | 14:30610615 | cccaaataaataaat[A/G]tatacataaatacat | 55632 |
rs229237 | snp | C/T | 0.483852 | 0.0883933 | intron-variant | G2E3 | GRCh38.p7 | 14:30610684 | GGGTTGGAGTATATA[C/T]AAGTTAGGTTTTAGG | 55632 |
rs229238 | snp | C/T | 0.177182 | 0.23916 | intron-variant | G2E3 | GRCh38.p7 | 14:30610777 | TTCTGTAAAATCCAT[C/T]GTCTAGATTTTAGGG | 55632 |
rs229239 | snp | A/G | 0.170408 | 0.236992 | intron-variant | G2E3 | GRCh38.p7 | 14:30611521 | CATAAATGGCCAAGT[A/G]TTTCTTTGTTTATGC | 55632 |
rs229240 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | G2E3 | GRCh38.p7 | 14:30611845 | TTTCTTTAGAGGGGG[A/G]CTAGCTGTGTTGCCC | 55632 |
rs229241 | snp | A/T | 0.14665 | 0.227637 | intron-variant | G2E3 | GRCh38.p7 | 14:30613710 | tttgttttttttttt[A/T]aaatcaaactttttt | 55632 |
rs229242 | snp | C/T | 0.178144 | 0.239451 | intron-variant | G2E3 | GRCh38.p7 | 14:30614032 | TAGTTTTTATTAACA[C/T]TTCATTTTATTTTAA | 55632 |
rs229243 | snp | A/C | 0.498964 | 0.02274 | intron-variant | G2E3 | GRCh38.p7 | 14:30614542 | AGCCCTTGTGACCTA[A/C]TCACCTCTTAAGGAC | 55632 |
rs229244 | snp | C/T | 0.498323 | 0.0289051 | intron-variant | G2E3 | GRCh38.p7 | 14:30615882 | CTAAATTATTCTTCA[C/T]CCACTGGTCAGGGCT | 55632 |
rs229245 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30616251 | TACTTTTGTTTCTTT[A/T]ACTCTTTTATTGGTA | 55632 |
rs229246 | snp | C/T | 0.199254 | 0.244796 | intron-variant | G2E3 | GRCh38.p7 | 14:30587378 | TAATATCTTAAGGCA[C/T]GAATTCAGTGAGGTG | 55632 |
rs229247 | snp | C/T | 0.483126 | 0.0902898 | intron-variant | G2E3 | GRCh38.p7 | 14:30588780 | CACATTCTACACTTT[C/T]TCTGATTCAGGCTTT | 55632 |
rs229248 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | G2E3 | GRCh38.p7 | 14:30590293 | GCATTTATGGGATAA[A/T]CTTTCTTTGACTTCT | 55632 |
rs229249 | snp | A/G | 0.15698 | 0.23205 | intron-variant | G2E3 | GRCh38.p7 | 14:30590306 | CTAAACAACTTCAGC[A/G]TTTATGGGATAATCT | 55632 |
rs229250 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | G2E3 | GRCh38.p7 | 14:30590544 | TATTTTTCCATCCTC[C/T]TTAATTTCCAGACTT | 55632 |
rs229251 | snp | A/C | 0.0151283 | 0.0856462 | intron-variant | G2E3 | GRCh38.p7 | 14:30590715 | CTCACCTTTCTCCCA[A/C]GGTTCTTCCTTGTGC | 55632 |
rs229252 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30591792 | gtacctgtgaatgtg[A/T]acttacttggaaata | 55632 |
rs229253 | snp | A/G | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30591815 | ttatgctcaggtccc[A/G]actcccagtacctgt | 55632 |
rs229254 | snp | A/T | 0.0456336 | 0.143994 | intron-variant | G2E3 | GRCh38.p7 | 14:30592074 | TAACATGTGGATAAG[A/T]CAGAGAAGCCCCTTT | 55632 |
rs229255 | snp | C/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30594129 | TGGTTCTTTGAGAGT[C/T]ATCTTACGTATCAAA | 55632 |
rs229256 | snp | C/T | 0.177503 | 0.239258 | intron-variant | G2E3 | GRCh38.p7 | 14:30594817 | TTAACTGAATAATCC[C/T]AAGTATAAAAGTTCA | 55632 |
rs229257 | snp | C/T | 0.029116 | 0.117091 | intron-variant | G2E3 | GRCh38.p7 | 14:30595247 | AACACTTCACAATGT[C/T]GTTTATTAACTGCAC | 55632 |
rs229258 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | G2E3 | GRCh38.p7 | 14:30596353 | TAGGGACTAAGGCCC[C/T]AGAGAAAGACCAACT | 55632 |
rs229259 | snp | C/G | 0.17332 | 0.23795 | intron-variant | G2E3 | GRCh38.p7 | 14:30597673 | CCAAGAACTGGCCAT[C/G]TGGGGGAGGAGAAGG | 55632 |
rs229260 | snp | A/C | 0.0858192 | 0.188533 | intron-variant | G2E3 | GRCh38.p7 | 14:30598194 | tttcgccatgttggc[A/C]aggctggtcttgaac | 55632 |
rs229261 | snp | C/T | 0.206642 | 0.246211 | intron-variant | G2E3 | GRCh38.p7 | 14:30598884 | ttggaaaagggaaat[C/T]tcaagtgctcaacag | 55632 |
rs369646 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30606664 | CCAGAGAGAGTTAGT[A/T]ATTAAGGATGTAAAG | 55632 |
rs396171 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30606668 | ACATCCTTAATAACT[A/T]ACTCTCTCTGGATCT | 55632 |
rs397632 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | G2E3 | GRCh38.p7 | 14:30600521 | GATGAAATAATGTAT[A/G]TAGAATTTTAAGAAG | 55632 |
rs412988 | snp | A/C | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30568707 | atgtaatttgacaca[A/C]taacatttaggaaga | 55632 |
rs447614 | snp | C/T | 0.483345 | 0.0897213 | intron-variant | G2E3 | GRCh38.p7 | 14:30611593 | AATTCTCAGCTGTTA[C/T]TCTTTTTCATGAATT | 55632 |
rs447853 | snp | G/T | 0.486464 | 0.0811471 | intron-variant | G2E3 | GRCh38.p7 | 14:30611594 | ATTCTCAGCTGTTAC[G/T]CTTTTTCATGAATTC | 55632 |
rs448175 | snp | G/T | 0.484632 | 0.086302 | intron-variant | G2E3 | GRCh38.p7 | 14:30599998 | TCATTTTGTGCATTT[G/T]AGGTACAGTGTACTG | 55632 |
rs764811 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30606202 | GAAAAATTGGTTACA[A/T]GTGGACCAGGAAACT | 55632 |
rs880979 | snp | C/T | 0.109814 | 0.206997 | intron-variant | G2E3 | GRCh38.p7 | 14:30587145 | TTCTCAGATTTATCA[C/T]TAGCAACAAATGAAA | 55632 |
rs1046062 | snp | G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617874 | TGGAAAACAAAGTCT[G/T]ATGTCCTTAATCTAT | 55632 |
rs1113946 | snp | A/G | 0.380919 | 0.21298 | intron-variant | G2E3 | GRCh38.p7 | 14:30571209 | atcactggtcataaa[A/G]gaaatgcacattaaa | 55632 |
rs1454977 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619608 | ACAATCCAAATTTTC[A/C]TAAACCACAGATAAT | 55632 |
rs1454978 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619550 | GGGTTATGTTTTGTA[A/C/T]TGCATTACTTGAAGC | 55632 |
rs1884582 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | G2E3 | GRCh38.p7 | 14:30611680 | TTTCTTTTTAAGAGA[G/T]AAGGTCTCAGTCTGT | 55632 |
rs2045180 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | G2E3 | GRCh38.p7 | 14:30609296 | TCCTATTTATTTCTT[A/G]TAATCAGGCTTCTGT | 55632 |
rs2273408 | snp | A/G | 0.0846438 | 0.187503 | intron-variant | G2E3 | GRCh38.p7 | 14:30592303 | TATGTTGTGACCCCT[A/G]TTTTCACATACTCTT | 55632 |
rs2273409 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30592525 | CCAATGATATAATAC[A/T]ACAATAAATTTTCTG | 55632 |
rs2273410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30592548 | ATTTTCTGTTTAGAG[C/T]ATCAGAGTTTAGATA | 55632 |
rs2295425 | snp | A/G | 0.109814 | 0.206997 | intron-variant | G2E3 | GRCh38.p7 | 14:30559593 | TAGTTTATTATTTCC[A/G]CCAATTCGGCTCGAA | 55632 |
rs2308298 | in-del | -/CATAATGATTTACCTAT | 0.495481 | 0.047319 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617943 | AAACATTTTACTTCC[-/CATAATGATTTACCTAT]CATAATGATTTACTT | 55632 |
rs2378767 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573447 | CGTGTGTGTGTGTCT[C/G]TGTGTGTGTAGAGAA | 55632 |
rs3031607 | in-del | -/TGTC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573442 | gtgtgcgtgtgtgtg[-/TGTC]tctgtgtgtgtagag | 55632 |
rs3825740 | snp | A/G | 0.381113 | 0.21286 | intron-variant | G2E3 | GRCh38.p7 | 14:30579169 | AGGAAGAAAAGAAAG[A/G]AAAAAATCCAAGAGA | 55632 |
rs3834537 | in-del | -/ATTT | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558588 | ACCATCAAATAGTTT[-/ATTT]GAGACCAGGAATTGG | 55632 |
rs4981073 | snp | C/T | 0.11228 | 0.208646 | intron-variant | G2E3 | GRCh38.p7 | 14:30559922 | AGACTCCTATTTAAA[C/T]CGGCTGTGGTAACAG | 55632 |
rs4981761 | snp | G/T | 0 | 0 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558281 | ACTGATCCGTTTAGG[G/T]AATTCAATGTTATTA | 55632 |
rs4981763 | snp | A/G | 0.139225 | 0.224118 | intron-variant | G2E3 | GRCh38.p7 | 14:30607511 | GTAATGCATTGTGCT[A/G]TGACAGTATAACATC | 55632 |
rs5807590 | in-del | -/TCTC | 0.145492 | 0.227108 | intron-variant | G2E3 | GRCh38.p7 | 14:30573444 | GTGCGTGTGTGTGTG[-/TCTC]TGTGTGTGTAGAGAA | 55632 |
rs6145285 | in-del | -/ACTGCATCATACGTGGGAAAAGTGTATCTATCCT | 0.49306 | 0.0584955 | intron-variant | G2E3 | GRCh38.p7 | 14:30602341 | AATACAAAATACCAA[lengthTooLong]ACTGCATCATACGTG | 55632 |
rs6145286 | in-del | -/CTGCATCATACGTGGGAAAAGTGTATCTATCCTA | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30602376 | AGTGTATCTATCCTA[lengthTooLong]ATTATTTTTTTGTGT | 55632 |
rs6571355 | snp | C/G | 0.106633 | 0.204807 | intron-variant | G2E3 | GRCh38.p7 | 14:30610792 | TGTCTAGATTTTAGG[C/G]Taagagttggcaaaa | 55632 |
rs7141624 | snp | A/G | 0.460027 | 0.135605 | intron-variant | G2E3 | GRCh38.p7 | 14:30587274 | AAAAGGAAACCAGTT[A/G]CTTTATGTATCACTC | 55632 |
rs7143519 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | G2E3 | GRCh38.p7 | 14:30605206 | TGGCCTGAGATTCTG[A/T]TTCTTAAACCGGAAT | 55632 |
rs7146136 | snp | A/G | 0.108048 | 0.20579 | intron-variant | G2E3 | GRCh38.p7 | 14:30571768 | gttctattgagctat[A/G]tatctgacttttccc | 55632 |
rs7147237 | snp | C/T | 0.111928 | 0.208413 | intron-variant | G2E3 | GRCh38.p7 | 14:30570411 | agtttttggctatta[C/T]ttcttcaaacattct | 55632 |
rs7154847 | snp | A/G | 0.475212 | 0.108534 | intron-variant | G2E3 | GRCh38.p7 | 14:30590763 | CGTGAGATGTTAAAC[A/G]TGAGATATTAGTATC | 55632 |
rs7156057 | snp | G/T | 0.0121185 | 0.0768921 | intron-variant | G2E3 | GRCh38.p7 | 14:30560815 | gtctggaggatggca[G/T]tgaacagtctgcata | 55632 |
rs7158970 | snp | C/T | 0.139225 | 0.224118 | intron-variant | G2E3 | GRCh38.p7 | 14:30604091 | TGAGATTTCCAAAGA[C/T]GCTACACCAGGGAAG | 55632 |
rs7159972 | snp | C/G | 0.124837 | 0.216412 | intron-variant | G2E3 | GRCh38.p7 | 14:30574520 | atattatttcatcac[C/G]caggtattaagccca | 55632 |
rs7160985 | snp | C/T | 0.143959 | 0.226396 | intron-variant | G2E3 | GRCh38.p7 | 14:30583512 | agtgctggttaccag[C/T]ggttgggaggattgg | 55632 |
rs7359107 | snp | C/T | 0.124837 | 0.216412 | intron-variant | G2E3 | GRCh38.p7 | 14:30582674 | GGTGGAGCTTACTGG[C/T]GTAGAATGTCCAATA | 55632 |
rs8004508 | snp | C/G | 0.139564 | 0.224285 | intron-variant | G2E3 | GRCh38.p7 | 14:30571622 | caatgttcttccccc[C/G]accctccgcccaaag | 55632 |
rs8005237 | snp | C/T | 0.17654 | 0.238964 | intron-variant | G2E3 | GRCh38.p7 | 14:30586968 | TTTTGTTTTTTGATA[C/T]TGAATTCTAAGATTC | 55632 |
rs8006170 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30604941 | cgctcttgttgccca[A/G]gctggagtgcaatgg | 55632 |
rs8009427 | snp | A/T | 0.381308 | 0.21274 | intron-variant | G2E3 | GRCh38.p7 | 14:30587809 | GAGAGAGAAATCAAG[A/T]TGGAACCATATGACC | 55632 |
rs8011158 | snp | G/T | 0.108048 | 0.20579 | intron-variant | G2E3 | GRCh38.p7 | 14:30588039 | TTGGTCCTCTAAGAC[G/T]ACAGTCTTGTGCCTC | 55632 |
rs8016482 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30582264 | aaccagtatcattta[C/T]tacactagacaccaa | 55632 |
rs8019014 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | G2E3 | GRCh38.p7 | 14:30614053 | TTTATTTTAAAATTA[C/T]ATAAAATGTTTTATA | 55632 |
rs8021430 | snp | A/G | 0.16976 | 0.236773 | intron-variant | G2E3 | GRCh38.p7 | 14:30582962 | TCTATTCTTGATTGC[A/G]tgtattattcaaggt | 55632 |
rs8022089 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | G2E3 | GRCh38.p7 | 14:30583111 | ttagggagtttctgc[A/G]gtatgcaatcattta | 55632 |
rs8022976 | snp | A/C | 0.125182 | 0.216612 | intron-variant | G2E3 | GRCh38.p7 | 14:30562202 | ccaggtgccgaggca[A/C]gagactgggggcacg | 55632 |
rs9806012 | snp | A/T | 0.0861826 | 0.188849 | intron-variant | G2E3 | GRCh38.p7 | 14:30568897 | tactggtgtttttat[A/T]tcctcgtatggcttt | 55632 |
rs10130242 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557442 | TTTCTAGCAATCTTC[C/T]TTAAAGAACAAAATT | 55632 |
rs10130571 | snp | A/G | 0.125182 | 0.216612 | intron-variant | G2E3 | GRCh38.p7 | 14:30587670 | gtcatgtggcttttg[A/G]cctcaatttctccta | 55632 |
rs10131312 | snp | C/G | 0.144296 | 0.226554 | intron-variant | G2E3 | GRCh38.p7 | 14:30575416 | caaacccacagccaa[C/G]attatactgaatggg | 55632 |
rs10132255 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | G2E3 | GRCh38.p7 | 14:30615854 | ATTTCATCATTTTCA[A/G]TTTGAAGTTAAACTA | 55632 |
rs10132507 | snp | C/T | 0.104504 | 0.2033 | intron-variant | G2E3 | GRCh38.p7 | 14:30563388 | TAAAGCCCCATACCA[C/T]TTAAAGTCCCATACC | 55632 |
rs10137652 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577346 | TTTTTtgtgttagtt[A/G]tctgttgtcgtgtaa | 55632 |
rs10139488 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | G2E3 | GRCh38.p7 | 14:30611192 | gaacagtcatgtagc[C/T]ccacctagctgcagc | 55632 |
rs10141104 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | G2E3 | GRCh38.p7 | 14:30578490 | GAGAGTGCAAACAAG[A/G]GGGACCACAGGGCTT | 55632 |
rs10142125 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | G2E3 | GRCh38.p7 | 14:30596265 | TCTACTTAGTATATT[C/T]TGTGTATCCTTTTTA | 55632 |
rs10142747 | snp | A/T | 0.125528 | 0.21681 | intron-variant | G2E3 | GRCh38.p7 | 14:30583772 | acattgtaagtatat[A/T]cagttttCTAAAAAA | 55632 |
rs10143105 | snp | A/G | 0.133435 | 0.221162 | intron-variant | G2E3 | GRCh38.p7 | 14:30584161 | gacttctttcactta[A/G]cataatatttctagg | 55632 |
rs10143362 | snp | G/T | 0.144632 | 0.226711 | intron-variant | G2E3 | GRCh38.p7 | 14:30575249 | tatctgcttatgtcc[G/T]ttggccactttttaa | 55632 |
rs10144613 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | G2E3 | GRCh38.p7 | 14:30579479 | AAAACACTTTTTACA[A/G]TCAGTATGAAATATA | 55632 |
rs10148278 | snp | A/G | 0.125528 | 0.21681 | intron-variant | G2E3 | GRCh38.p7 | 14:30590833 | AAAGGTGGTCTCTAA[A/G]GGTCCCCTTATGGTT | 55632 |
rs10148782 | snp | A/G | 0.103082 | 0.202275 | intron-variant | G2E3 | GRCh38.p7 | 14:30598319 | ttgaacccggcaggc[A/G]gaggttgcagtgacc | 55632 |
rs10148858 | snp | C/T | 0.154329 | 0.23097 | intron-variant | G2E3 | GRCh38.p7 | 14:30613795 | ATGATTTTTACTTAA[C/T]ATTTTCTTTGTCCTG | 55632 |
rs10152019 | snp | C/G | 0.0861826 | 0.188849 | intron-variant | G2E3 | GRCh38.p7 | 14:30599552 | cttaaaaggccttat[C/G]tccatatatagtcac | 55632 |
rs10152074 | snp | G/T | 0.0861826 | 0.188849 | intron-variant | G2E3 | GRCh38.p7 | 14:30599431 | atcgggtttcaccat[G/T]ttggtcagcctggtc | 55632 |
rs10450882 | snp | A/G | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30585783 | tctttaaattgtaaa[A/G]gtaggttattgattt | 55632 |
rs10552989 | in-del | -/TG | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573410 | AGAAACAACAGGATA[-/TG]TGTGTGTGTGTGTGT | 55632 |
rs10582820 | in-del | -/AG | 0.084364 | 0.187256 | intron-variant | G2E3 | GRCh38.p7 | 14:30581392 | GAGAACAATTTAAAC[-/AG]TGTGTAAAAGTTTAA | 55632 |
rs11322769 | in-del | -/T | 0.495368 | 0.0478996 | intron-variant | G2E3 | GRCh38.p7 | 14:30584846 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 55632 |
rs11389797 | in-del | -/T | 0.476746 | 0.10529 | intron-variant | G2E3 | GRCh38.p7 | 14:30560085 | TGCTTTGAGCATCTG[-/T]TTTCTTTGGGTTTTA | 55632 |
rs11411112 | in-del | -/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573008 | ATGTACTTTTTTTTT[-/T]GGATGGAGGTCTCAC | 55632 |
rs11451039 | in-del | -/T | 0.456803 | 0.140473 | intron-variant | G2E3 | GRCh38.p7 | 14:30571176 | TGCTTTTTTTTTTTT[-/T]GCTATTTTAATGTGC | 55632 |
rs11621771 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | G2E3 | GRCh38.p7 | 14:30593154 | CGATTTTGAGCACAA[A/C]GTATGCACCCATTTG | 55632 |
rs11622127 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30609035 | gaatgccaactctta[A/T]aactactatatgttg | 55632 |
rs12147077 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30569923 | GAATGCTTTTTCTGC[C/G]TTGTCTGCTCAGAAT | 55632 |
rs12323506 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617424 | gttgttgttgttTGT[A/G]TCCTATGTTTGGTAT | 55632 |
rs12434151 | snp | A/G | 0.476746 | 0.10529 | intron-variant | G2E3 | GRCh38.p7 | 14:30559979 | TTGCAAACAATAGGG[A/G]TAAGGTTTAGTTCCA | 55632 |
rs12435014 | snp | A/G | 0.0240643 | 0.107019 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619319 | GAACTTTTGTATTCA[A/G]TGCTAAATACTAAGT | 55632 |
rs12885353 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | G2E3 | GRCh38.p7 | 14:30609368 | CCAGGGAGCTAAATA[C/T]CCATGTCCAAAGGCC | 55632 |
rs12891879 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573440 | GTGTGTGCGTGTGTG[C/T]GTGTCTCTGTGTGTG | 55632 |
rs12893188 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598324 | cccggcaggcggagg[A/T]tgcagtgacctgaga | 55632 |
rs12893201 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598341 | gcagtgacctgagat[C/T]gcaccactgtactcc | 55632 |
rs12894186 | snp | A/G | 0.452597 | 0.146474 | intron-variant | G2E3 | GRCh38.p7 | 14:30586169 | ctcatccctcaggga[A/G]ccatcatacaggtca | 55632 |
rs13343233 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577238 | caaaaaaaaaaaaaa[A/G]aaaaagaaaaagaaa | 55632 |
rs17096909 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559189 | GGCCGTTGAATGTGG[C/T]TGCTCGCGGTCGGCG | 55632 |
rs17096912 | snp | G/T | 0.0193772 | 0.0965046 | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559206 | GCTCGCGGTCGGCGT[G/T]CCCCGACGTACAGCG | 55632 |
rs17096931 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | G2E3 | GRCh38.p7 | 14:30591995 | TGAGATTTCAATGAG[C/G]TGTTTATGTATATAG | 55632 |
rs17096934 | snp | A/G | 0.0094609 | 0.0681244 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598542 | TGCAGCACTATGAGC[A/G]TTGTGATGTTCGAAG | 55632 |
rs17096939 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | G2E3 | GRCh38.p7 | 14:30600148 | TACTTAACATAGTAA[A/G]CTCAGTGTATAGAGC | 55632 |
rs17096940 | snp | C/T | 0.102014 | 0.201495 | intron-variant | G2E3 | GRCh38.p7 | 14:30601395 | CCTCACCTTGAAATT[C/T]ACTGAATGTTTCTTC | 55632 |
rs17096941 | snp | A/G | 0.45235 | 0.146814 | intron-variant | G2E3 | GRCh38.p7 | 14:30603416 | ATCTTTATAATGTTG[A/G]GTATTTGTTCAGCTG | 55632 |
rs17096955 | snp | A/G | 0.140242 | 0.224618 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618263 | TTTTGTCTCACCAAT[A/G]GTAATTGAAAGATCA | 55632 |
rs17348231 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30561740 | TGCAGTGCACAGTGC[A/G]GAACAGTGAGTGTCA | 55632 |
rs17348259 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30561910 | ATTCTGTGTAGTTTA[A/G]TAGAGATTTTAGTGA | 55632 |
rs17348844 | snp | A/G | 0.103794 | 0.20279 | intron-variant | G2E3 | GRCh38.p7 | 14:30607172 | GTAATTTTGAGTAGT[A/G]TGATAAAAAGTTTAC | 55632 |
rs17433265 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30593119 | TTTAGGCGTAAGTTC[C/T]TGCCTCCCTTAATTT | 55632 |
rs28367069 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30560359 | GTACCATTTAAATGT[A/G]TAAATATATTTTTAA | 55632 |
rs28542564 | snp | C/G/T | 0.0364509 | 0.129988 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559111 | CGGGTCCCACCCCTC[C/G/T]AGGGCGGGGCCGACC | 55632 |
rs28679478 | snp | G/T | 0.17461 | 0.238362 | intron-variant | G2E3 | GRCh38.p7 | 14:30615018 | ATTAGCTTTGAAGTG[G/T]AAAACACTTCAGATT | 55632 |
rs28721907 | snp | G/T | 0.106278 | 0.204558 | intron-variant | G2E3 | GRCh38.p7 | 14:30581512 | AAGAGTTCAAGACCA[G/T]CCTGGCCAACATGAC | 55632 |
rs28761255 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566015 | ACCATTTGTCGAAGA[A/G]ACTGTTTTCTTCCCA | 55632 |
rs28856403 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566013 | GGACCATTTGTCGAA[A/G]AGACTGTTTTCTTCC | 55632 |
rs33919348 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611827 | ACCAGGCCTTTTTTT[-/T]TTTTTCTTTAGAGGG | 55632 |
rs33950296 | in-del | -/TAAG | 0.0325976 | 0.123435 | intron-variant | G2E3 | GRCh38.p7 | 14:30587735 | GGGCCTCTTAGTAAA[-/TAAG]GCTACTCGTGGCATG | 55632 |
rs34009891 | in-del | -/T | | | splice-acceptor-variant | G2E3 | GRCh38.p7 | 14:30593471 | ATAATTTACATTTTT[-/T]AGGTCATTTTGTTGG | 55632 |
rs34080508 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609459 | TTTTATTTAATATTG[G/T]ACTTCCTCCTACTTC | 55632 |
rs34158873 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561949 | GTTTATAAACTATGG[-/G]AAAAATAAGTATTGA | 55632 |
rs34394325 | in-del | -/T | 0 | 0 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557903 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGCCTCGC | 55632 |
rs34534669 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564514 | ATTAAAAATTTTTTT[-/T]ATAGAGACAGGATAT | 55632 |
rs34558066 | multinucleotide-polymorphism | CT/TG | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30611593 | AATTCTCAGCTGTTA[CT/TG]CTTTTTCATGAATTC | 55632 |
rs34628893 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30577866 | CAGTGGAGGACACTC[-/C]AGAATACCTTTTGAC | 55632 |
rs34632872 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578106 | GTACTTATTTTTTTT[-/T]ACTAAGGTTTTGTTT | 55632 |
rs34646170 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585197 | TATCATTTTTTTCTT[-/C]TTGTTACCTGTGCTT | 55632 |
rs34653368 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588545 | TACTTTAAAAAAAAA[-/A]GTACTGACCCCAGAC | 55632 |
rs34654755 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619427 | AAATCATTACATTAT[-/T]AAACATGTAATTCTT | 55632 |
rs34657970 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561673 | CCAGGCTGTGCTTTT[-/T]GCTTATAAATATATA | 55632 |
rs34689464 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572447 | GTCAGATGCCCTTTT[-/T]GTATCTGTTGACATT | 55632 |
rs34696810 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559997 | GGTTTAGTTCCACCG[-/G]CCCTGCCTTTTCGCC | 55632 |
rs34718480 | in-del | -/A | 0.49934 | 0.0181589 | intron-variant | G2E3 | GRCh38.p7 | 14:30571944 | TAAAAAAAAAAAAAA[-/A]CCTGCTGGGGATTTT | 55632 |
rs34755731 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567780 | ATTTTCTAATTTCCC[-/C]TTGTGATTTCTTTTT | 55632 |
rs34835272 | in-del | -/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577339 | ACTTACTTTTTTTGT[-/G]TTAGTTATCTGTTGT | 55632 |
rs35145826 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618954 | TGTTGTATATTTTAA[-/A]GGCTGTTTTCTCTTG | 55632 |
rs35170058 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565200 | AGTGGTGTCTCATTG[G/T]GGCTTTGATTTACTT | 55632 |
rs35199414 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604739 | TTGTGTAATCTCTCA[-/A]AAGACATTTTCTTAT | 55632 |
rs35256959 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606249 | CAATATTTTTTTTTT[-/T]GCACAATTATGTATA | 55632 |
rs35290629 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607613 | CACAACATCCTTATA[-/A]TGGTGCATGACTGTA | 55632 |
rs35325923 | in-del | -/ATAA | 0.00716266 | 0.059414 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619807 | TTATAACAATGTTTT[-/ATAA]ATAAATAAATGTGTT | 55632 |
rs35389182 | snp | C/T | 0.454061 | 0.144427 | intron-variant | G2E3 | GRCh38.p7 | 14:30585586 | TTAATCTTCTCCCCC[C/T]TTTTTTTTTTGGTTA | 55632 |
rs35395254 | snp | G/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577338 | GACTTACTTTTTTTG[G/T]GTTAGTTATCTGTTG | 55632 |
rs35460421 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564484 | CTACAGGCATTTGCC[-/C]ACCAAGACTGGCTAA | 55632 |
rs35533577 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594321 | TAAGTTTAATACTGT[-/G]TTTTTAAAGTTTATT | 55632 |
rs35547053 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610388 | GGGAGAACAGGTGGG[-/G]TGGATCACCGGGGTC | 55632 |
rs35621800 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564215 | GTTACAGTTTTTAGT[-/G]TATCACAAATAAAGT | 55632 |
rs35692497 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619974 | TAGTGTCTGACACCC[-/C]AGGAACCTATAGAAA | 55632 |
rs35763157 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615035 | AACACTTCAGATTTT[-/T]GATGTCTTTCTTACT | 55632 |
rs35812314 | in-del | -/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558548 | CCTTATCTGAGGGGG[-/G]AAATAAAATTTATTG | 55632 |
rs35889068 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585179 | ATTTTAATGAAGTCC[-/C]AATTATCATTTTTTT | 55632 |
rs35932465 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570071 | TTTGAAACATAGTTT[-/T]GCTGCAGATAGGATT | 55632 |
rs36045944 | in-del | -/TTAA | 0.031825 | 0.122064 | intron-variant | G2E3 | GRCh38.p7 | 14:30579535 | ATAAGTTTAATTTGG[-/TTAA]TCAGTCTTCATAAAA | 55632 |
rs45443103 | snp | C/T | 0.0596104 | 0.162024 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617775 | AATACCTAAAAGTAA[C/T]TGTACTAACAAAGTG | 55632 |
rs45472591 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619325 | TTGTATTCAGTGCTA[A/G]ATACTAAGTCAAGGG | 55632 |
rs45475495 | snp | A/G | 0.0115128 | 0.0749924 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616319 | GACATTCTTATTTTT[A/G]CAACTGGTTGCAGTT | 55632 |
rs45502891 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30590853 | CCCTTATGGTTTGGA[A/G]CTACAGATTGAATAT | 55632 |
rs45531233 | snp | C/G | 0.0182019 | 0.0936463 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618693 | TTTGCAAAATGTTTT[C/G]TAGTTTGAAGGATGT | 55632 |
rs45567332 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30616006 | TAGCTAGATTTTTGG[A/T]TTTTTACCGTTTAGT | 55632 |
rs45573134 | snp | C/G | 0.0209421 | 0.100162 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619001 | AAACTATAAATTGAT[C/G]TATAATGCATCTACT | 55632 |
rs55882754 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570106 | GCTTACAGGTTTGGG[G/T]TTTTTTCCTGTCTTT | 55632 |
rs56763211 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603162 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAT | 55632 |
rs56962489 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603170 | GTCTCTATTAAAAAT[A/T]CAAAAATTAGCTGGG | 55632 |
rs57466700 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603195 | GCTGGGCATAGTGTT[A/G]TGCATCTGTAGTCCC | 55632 |
rs57486316 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614243 | GATAAACATGTGTGT[-/GT]TCTTAGCTCATTTTA | 55632 |
rs57633285 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603102 | GGAAACCTAGGCGGG[A/C/T]GGATCCCGAGGTCAA | 55632 |
rs57677010 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30608726 | TTAAAAACTGAGACA[A/G]TGCAAGCCATTTAAC | 55632 |
rs57751550 | in-del | -/CTCT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573445 | TGCGTGTGTGTGTGT[-/CTCT]GTGTGTGTAGAGAAG | 55632 |
rs57795359 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | G2E3 | GRCh38.p7 | 14:30578846 | AAGATGGACTCAACC[C/T]TTCTACACACACGCT | 55632 |
rs58133695 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603137 | TCGAGAACATCCTGG[C/G]CAATATGGTGAAACC | 55632 |
rs58231764 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | G2E3 | GRCh38.p7 | 14:30607662 | GGTTATTATGGTGGT[A/G]GGTTTATTGTGTTTT | 55632 |
rs59447041 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603107 | CCTAGGCGGGCGGAT[A/C]CCGAGGTCAAGAGAT | 55632 |
rs59557580 | in-del | -/GGTG/TGTGTGTGTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563739 | GTGTGTGTGTGTGTG[-/GGTG/TGTGTGTGTG]ATATAGAGTCTCACT | 55632 |
rs59660692 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30566480 | GTTAAATTTATTACT[A/G]AGTAATTTTTATGCT | 55632 |
rs59672554 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596136 | TGTGTGTGTGTGTGT[-/GT]CACTTGCTAATTGTC | 55632 |
rs59757142 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577243 | AAAAAAAAAAAAAAA[-/AA]GAAAAAGAAAAAATG | 55632 |
rs59896171 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603079 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAAACCT | 55632 |
rs60350877 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30561818 | AATTTAACACATTTT[G/T]TCTTGGGTTAATGAC | 55632 |
rs60353606 | snp | A/G | 0.00261878 | 0.0360906 | intron-variant | G2E3 | GRCh38.p7 | 14:30560785 | CACTTCAGATCTCAG[A/G]TTCTGAATCAGTAGG | 55632 |
rs60362029 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30587546 | AGGGTCAGGAATTTG[G/T]CTGAGCTGGATAGTT | 55632 |
rs60495765 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603183 | ATACAAAAATTAGCT[A/G]GGCATAGTGTTGTGC | 55632 |
rs60676717 | snp | C/G | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601894 | ATTATCTACAATTCA[C/G]GTAATTTTTTTGTAA | 55632 |
rs60825630 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30579717 | TGCAGTCACTCAGTT[A/G]TGGGTTAGTGTATTC | 55632 |
rs60907760 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603082 | CCTGTAATCCCAGCA[C/T]TTTGGGAAACCTAGG | 55632 |
rs61225908 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561860 | TGCTTTTTTTTTTTT[-/T]AAGGCTTGGCTTTTT | 55632 |
rs61734966 | snp | A/G | 0.0259695 | 0.110952 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586778 | GAGAAAAGAAAACTA[A/G]GGAGAAATGGAATCT | 55632 |
rs61740181 | snp | A/G | 0.000116441 | 0.00762933 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616337 | ACTGGTTGCAGTTCC[A/G]TTCCTCCAGCTGGAT | 55632 |
rs61976688 | snp | A/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558728 | AGGACTGAGAGGCCC[A/T]GGAAAGGCTGCACTA | 55632 |
rs61976689 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | G2E3 | GRCh38.p7 | 14:30563480 | ACCATTCATGTGATT[C/T]CTTGATTTTGGAGTT | 55632 |
rs61976690 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573018 | TGTACTTTTTTTTTG[G/T]ATGGAGGTCTCACTA | 55632 |
rs61976691 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573432 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTCTC | 55632 |
rs61976692 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | G2E3 | GRCh38.p7 | 14:30574657 | TTTAGCTCCCACTTA[A/C]AAGTGAGAACATGCG | 55632 |
rs61976693 | snp | G/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30580201 | ATAAAGGATTGTTTT[G/T]GTTTTTTTTTGTTGT | 55632 |
rs61976694 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | G2E3 | GRCh38.p7 | 14:30585018 | TGTATTTTTTTTTAG[C/T]AGAGATGGGGTTTCA | 55632 |
rs61976695 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30592732 | TAATTCAGTGAAAAT[A/C]TCCACCTTTACATAA | 55632 |
rs61976696 | snp | A/C/T | 0.0150606 | 0.0854603 | intron-variant | G2E3 | GRCh38.p7 | 14:30594990 | AAAAAAAAAAAAAAT[A/C/T]AGCTGGGCGTGGTGG | 55632 |
rs61976706 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618512 | ACACATACTTTGTTG[A/G]GGTGGGGGTGGCAGG | 55632 |
rs71112331 | in-del | -/GT | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30596165 | TGTGTGTGTGTGTGT[-/GT]CACTTGCTAATTGTC | 55632 |
rs71415947 | snp | C/G/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30570167 | TCTGGAACTCTATGG[C/G/T]TTCTAATGAGAATTT | 55632 |
rs71443373 | in-del | -/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30598107 | ATTTTAGGCCAGGCA[-/T]TGGTGGCTCACGCCT | 55632 |
rs71443374 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30604738 | ATTGTGTAATCTCTC[-/A]AAAGACATTTTCTTA | 55632 |
rs71973374 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573421 | GATATGTGTGTGTGT[-/GT]GTGTGTGTGCGTGTG | 55632 |
rs72666415 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559015 | AGCGAAGGCGACACA[A/G]CCAGGTTAGCACCGA | 55632 |
rs72666416 | snp | C/G | 0.190833 | 0.242898 | intron-variant | G2E3 | GRCh38.p7 | 14:30567285 | GGGTTCACCAGTGAA[C/G]CCATCTGGGCTAGGA | 55632 |
rs72666417 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572032 | ATGAGCATTGTCTAT[C/G]TCTTCATTTATTTAG | 55632 |
rs72666418 | snp | A/G | 0.067446 | 0.170804 | intron-variant | G2E3 | GRCh38.p7 | 14:30580676 | ATATAATTTGTTAAT[A/G]TGTAAAATGGGCTTA | 55632 |
rs72666419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30590858 | ATGGTTTGGAACTAC[A/G]GATTGAATATCCCTT | 55632 |
rs72666421 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597702 | GGAAAGCAGGGACTG[G/T]GTCATAAATGTCTCA | 55632 |
rs72666423 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | G2E3 | GRCh38.p7 | 14:30600828 | GTGAACTTGAGTGGA[C/G]AAGTTATTGACCCCT | 55632 |
rs72666424 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612973 | CTTACCACATGAGCC[A/C]ACTATTCTGTCTCTG | 55632 |
rs73251125 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | G2E3 | GRCh38.p7 | 14:30611069 | TCATTATCGTGTAAC[A/G]CTTAGCATTATTGTT | 55632 |
rs73251128 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | G2E3 | GRCh38.p7 | 14:30611438 | ATTTTCTGTTAATGG[A/G]TTGTTTCCTATTTTT | 55632 |
rs73251132 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | G2E3 | GRCh38.p7 | 14:30611984 | TATAAATAGTTTCAC[A/G]TAGTAAAGTGGCATT | 55632 |
rs73251134 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | G2E3 | GRCh38.p7 | 14:30612882 | AAAAAGAATTGTGTA[A/C]ATGTATGATGCTTTC | 55632 |
rs73258118 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30567104 | AGGATATTTGCATCT[A/G]TGTTCATAAGAGATA | 55632 |
rs73258119 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30570943 | GTCTTATTCTCTTAA[C/T]AGTGTCTTTTGATGA | 55632 |
rs73264305 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | G2E3 | GRCh38.p7 | 14:30572459 | TTTTGTATCTGTTGA[C/G]ATTGTGTCACAGTAC | 55632 |
rs73264309 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30572888 | AAACATATAGAACAT[G/T]AAGGAAAGTCTAAAC | 55632 |
rs73264311 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30573238 | CCATTGAATGTCTTT[A/C]TTCTAATTTTATCTT | 55632 |
rs73264321 | snp | C/G | 0.0429648 | 0.14013 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577530 | ATGAAGGCTTGATTG[C/G]GGCTGGAGGATTCAC | 55632 |
rs73264322 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30579056 | TGTGATCCTCAATCA[A/G]TTTGTTCACTTAAGG | 55632 |
rs73264329 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30581479 | TACGAGGCTGAAGCA[A/G]GCAAATCACTTGAGG | 55632 |
rs73264330 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30582153 | TTGCCAAATGCAAAT[A/G]CACATCTACTATTGA | 55632 |
rs73264333 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30586019 | TTTCAGTCTATCTGC[C/T]GCTTTCCCTATCTGT | 55632 |
rs73264341 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30591562 | CCATGCTTCTCCCCT[A/G]GCTTCACATGGCTGC | 55632 |
rs73264346 | snp | A/G | 0.0119249 | 0.0762907 | intron-variant | G2E3 | GRCh38.p7 | 14:30598448 | TATGTAACATTATTT[A/G]TAGGTCAAAGCATAT | 55632 |
rs73264350 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | G2E3 | GRCh38.p7 | 14:30600917 | ATTGTGAGGATTAAA[C/T]TTTTCATATGAACAC | 55632 |
rs73264352 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30602895 | GGGATTACAGGTGTG[C/T]GCCACTATGCCCTGC | 55632 |
rs73264353 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30604316 | AAGCAAAACCTGGCC[C/T]ACACTAGGGCACTGT | 55632 |
rs73264358 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | G2E3 | GRCh38.p7 | 14:30606269 | AATTATGTATATGAT[A/G]GTTTTCTGTCTTCAC | 55632 |
rs73264361 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | G2E3 | GRCh38.p7 | 14:30606836 | CAAAGTTGCTAATAC[A/T]TTTGAAATGACAATT | 55632 |
rs73264362 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30608302 | CAGTTGGATAATGTG[A/G]TTTTGGTCTGTGTTC | 55632 |
rs74041244 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30580788 | TTGTGTAGGACTGTT[C/T]GGAGCATTGCAAGAT | 55632 |
rs74519441 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | G2E3 | GRCh38.p7 | 14:30570800 | CCTGCAGAGCCCCTT[A/G]CTCCACCATTTTCGT | 55632 |
rs74649757 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30600526 | AATAATGTATATAGA[A/C]TTTTAAGAAGCAATA | 55632 |
rs74677085 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | G2E3 | GRCh38.p7 | 14:30566272 | CTTAGCTTTTCCATT[A/C]CTGCAAAAAAAGGCC | 55632 |
rs74688573 | snp | C/G/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30560110 | GTTTTATTGTTTTGG[C/G/T]CTTTTTTTTTTTTAA | 55632 |
rs74706268 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | G2E3 | GRCh38.p7 | 14:30600722 | AGTGAGAAGAAGGCA[A/G]TTTTAGTGAAAGGCA | 55632 |
rs74781994 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30561849 | TCAAAAAGTTGTTGC[C/T]TTTTTTTTTTTAAGG | 55632 |
rs74802233 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | G2E3 | GRCh38.p7 | 14:30600628 | TTGGTCTCTCAATCA[A/G]TAGCTACAACTCTTC | 55632 |
rs74838479 | snp | A/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30594543 | AAATACAAAAAAAAA[A/T]TTAGCCGGGCATGGT | 55632 |
rs74900089 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30570435 | ACATTCTTTCTGTTC[C/T]ACTTTCTCCGGTCCC | 55632 |
rs74951663 | snp | C/G | 0.0577344 | 0.159793 | intron-variant | G2E3 | GRCh38.p7 | 14:30561358 | ATATTTCTTGCCTCT[C/G]TTCAGTCTCCCTCCA | 55632 |
rs74956779 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | G2E3 | GRCh38.p7 | 14:30610144 | GTTTCTGTACTTTTT[A/G]TCCAGTGTTTGTTCA | 55632 |
rs74976084 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | G2E3 | GRCh38.p7 | 14:30587057 | TTTTTCTTTCTTTCT[G/T]TTTAAGGCCTAAGTG | 55632 |
rs75014526 | snp | C/G/T | 0.0337553 | 0.125452 | intron-variant | G2E3 | GRCh38.p7 | 14:30585665 | TTTTTTTTTTTACTC[C/G/T]CTCTATTGTTTTTCC | 55632 |
rs75067601 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30579413 | GAGATTTGAACTATG[A/C]CTTTTTAGGAAAGCA | 55632 |
rs75318181 | snp | G/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573016 | TATGTACTTTTTTTT[G/T]GGATGGAGGTCTCAC | 55632 |
rs75365601 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30583020 | AACCCTGACATCTTA[C/G]TGGTTTAAAACAAGA | 55632 |
rs75469248 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | G2E3 | GRCh38.p7 | 14:30566641 | TTTTGTGAATTCTGT[A/G]GGAAATTCTACATAT | 55632 |
rs75470974 | snp | A/G | 0.0425829 | 0.139564 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619728 | TTATGCTAGGTGATC[A/G]TTTATATGTCAGCCT | 55632 |
rs75471738 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | G2E3 | GRCh38.p7 | 14:30580536 | AGGCTGCACAAATAC[A/G]AATGGCATGGCTATT | 55632 |
rs75583958 | snp | A/G | 0.144969 | 0.226867 | intron-variant | G2E3 | GRCh38.p7 | 14:30568027 | GGTGGAGTGTTCTGT[A/G]TATGTTAAGTCTAAA | 55632 |
rs75741795 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | G2E3 | GRCh38.p7 | 14:30582128 | TACTTCATGGACTAC[C/T]TCTATGCATTTGCCA | 55632 |
rs75831977 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598578 | GTTGCAAAGAAGGGC[A/G]AGACTATAATGCACC | 55632 |
rs76069579 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30583457 | GCATAATCTCCCTTA[C/T]GTGTGGAATATAAAA | 55632 |
rs76081304 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | G2E3 | GRCh38.p7 | 14:30588109 | GAGCTTATTTATAAG[A/G]GAACATGAAGTTGTC | 55632 |
rs76225334 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560124 | GGCTTTTTTTTTTTT[A/T]ATTTTTAATGATGAA | 55632 |
rs76227544 | snp | A/G | 0.00438476 | 0.0466401 | intron-variant | G2E3 | GRCh38.p7 | 14:30591776 | ACATCTGCAAAGACC[A/G]TATTTCCAAGTAAGT | 55632 |
rs76296662 | in-del | -/TT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585659 | ACCAACTTTTTTTTT[-/TT]ACTCCCTCTATTGTT | 55632 |
rs76362563 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30579989 | ATCTTTTAGAGAAAA[A/G]TTATATTTCAGTAAT | 55632 |
rs76421995 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30567123 | TCATAAGAGATAATT[G/T]GCTTGTAGTTTTATT | 55632 |
rs76447389 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30565013 | GTGGAATTGCTGGGT[C/G]ATATGGTAGTCTTGT | 55632 |
rs76475202 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30568538 | ATTTTGATTCCCTTC[G/T]CATTACCTTTTCTGC | 55632 |
rs76536965 | in-del | -/T | 0.419456 | 0.183806 | intron-variant | G2E3 | GRCh38.p7 | 14:30599225 | TACTGTAATTACCTC[-/T]TTTTTTTGTTTGTTT | 55632 |
rs76554654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30606415 | ATGAGAAGGCATTTC[A/G]TTTCATTTGAATTTC | 55632 |
rs76680406 | snp | A/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30594988 | ACAAAAAAAAAAAAA[A/T]TTAGCTGGGCGTGGT | 55632 |
rs76689091 | snp | G/T | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615534 | GTTACTTACAGGCTG[G/T]TGAAGGTATGTGGAT | 55632 |
rs76815703 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30582183 | ATACTTTTTCCTAAG[A/G]TGGACTGTTTCTTTA | 55632 |
rs76941714 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | G2E3 | GRCh38.p7 | 14:30584132 | AGTAATATTGTGACC[C/T]TTTGTGTGTGTTTGA | 55632 |
rs76991813 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30578858 | ACCCTTCTACACACA[C/T]GCTTCTTTCCATATG | 55632 |
rs77060693 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | G2E3 | GRCh38.p7 | 14:30564830 | CACATAATCATTCTA[C/T]GGATATACCACATTT | 55632 |
rs77210383 | snp | A/C | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30603325 | GCCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 55632 |
rs77257173 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | G2E3 | GRCh38.p7 | 14:30588055 | ACAGTCTTGTGCCTC[C/T]GTACCTCAAAGGTTA | 55632 |
rs77399321 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30587049 | TTTGTTTGTTTTTCT[C/T]TCTTTCTGTTTAAGG | 55632 |
rs77422280 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | G2E3 | GRCh38.p7 | 14:30566290 | GCAAAAAAAGGCCAT[C/T]GGGATTTTGACAGGA | 55632 |
rs77659779 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | G2E3 | GRCh38.p7 | 14:30614661 | CACTCTAAAACTCAC[A/G]TCCCACTCACATACA | 55632 |
rs77728446 | snp | A/G | 0.116138 | 0.211142 | intron-variant | G2E3 | GRCh38.p7 | 14:30570788 | GGGAGGTACAGGCCT[A/G]CAGAGCCCCTTGCTC | 55632 |
rs77810288 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | G2E3 | GRCh38.p7 | 14:30585134 | CCACTGTACCCAGAC[A/G]ATAGTGTCCTTTGAG | 55632 |
rs77956026 | snp | A/G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570525 | CTCTGTTTATTTTTC[A/G/T]TTTTTTTTCTTTCTG | 55632 |
rs78186086 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607091 | AGCCAGGATAGCCAG[G/T]GGGATGGTTTGCATT | 55632 |
rs78255549 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | G2E3 | GRCh38.p7 | 14:30595868 | CTATCAAAGAAACTG[G/T]TAAAAACTTTCCACT | 55632 |
rs78347978 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30608454 | ATGGGTCTGAAGAGA[C/G]GAAGGATTTGGCTTA | 55632 |
rs78584376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30582109 | ATAGTTCTGAAACTT[C/T]TAGTACTTCATGGAC | 55632 |
rs78641421 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30566567 | AAATACAACTGATAT[C/T]TGTGTGTTGATCTTG | 55632 |
rs78673303 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | G2E3 | GRCh38.p7 | 14:30571260 | GTTGGCTATGTTGTG[G/T]TTTTTTTAAATGTCT | 55632 |
rs78845581 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30584051 | GCCCCTGGTAACCAC[C/T]AATCTGCTTTTTGTG | 55632 |
rs78907633 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618285 | GAAAGATCAATTATC[A/G]AAGAGTTTGAATAGC | 55632 |
rs79044385 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | G2E3 | GRCh38.p7 | 14:30560706 | TCTTTCTTAAATCAG[G/T]GAGTTTCAGAATTTA | 55632 |
rs79063171 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569685 | CTTGGTCAGTGGAAG[A/G]GGCTAGGACTGGAAT | 55632 |
rs79081050 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | G2E3 | GRCh38.p7 | 14:30563777 | CCAGGCTGAATGCAA[C/T]GGTGGGATCTTGACT | 55632 |
rs79083880 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30579283 | TAAAGCCCCCTTAAA[A/G]CTGGGCTCTTAGTTG | 55632 |
rs79231674 | snp | C/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573445 | TGCGTGTGTGTGTGT[C/G]TCTGTGTGTGTAGAG | 55632 |
rs79235652 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30572880 | TCAGGAAAAAACATA[C/T]AGAACATGAAGGAAA | 55632 |
rs79355486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30563354 | TCATGACCAGTAGGT[A/C]GGGTTGGTCTAAGGG | 55632 |
rs79514931 | snp | C/T | 0.109814 | 0.206997 | intron-variant | G2E3 | GRCh38.p7 | 14:30568379 | TCAACCTTTGCCTTT[C/T]AATTGGAGCGTGTAA | 55632 |
rs79675928 | snp | G/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30565654 | CAACTTCATTCCTTT[G/T]TTTTTTTTTTTTTTT | 55632 |
rs79851970 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30602975 | GAGTCTAAATGTCAG[C/T]TCTTCCCTTTAGAAA | 55632 |
rs79891504 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | G2E3 | GRCh38.p7 | 14:30592815 | GGCTGTATGCATTTC[A/G]AGTAAATCAAAGGCA | 55632 |
rs79956632 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577204 | CAATCCAGCCTAGCA[A/G]CAGAGCAAGACTCTG | 55632 |
rs79980516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574052 | AGAAAAGTACAAAGA[A/G]CTACATATGCCCTTA | 55632 |
rs80176698 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | G2E3 | GRCh38.p7 | 14:30599867 | AGATGAATCTAGTTA[C/T]ATTACCCTCTAGAAC | 55632 |
rs80199187 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | G2E3 | GRCh38.p7 | 14:30605974 | TGGGAAGGGGGAGTG[A/G]TAGTTTAAAAAGTAA | 55632 |
rs80354670 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30565085 | ATCATTTTACTTTCC[A/C]ACTAGCAATATGTAA | 55632 |
rs111233474 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612224 | AAATACTGCAACAAC[C/T]GTAGCTGACTTAAAG | 55632 |
rs111432724 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30569603 | TTTATTGCCTGAACT[A/G]TAGTAAAAAAGATGC | 55632 |
rs111479046 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577460 | TTAGCTGTGTGGTTC[C/T]GGCTTAGGGTCTTGT | 55632 |
rs111497035 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30584947 | AGCAATTCTTCTTCC[G/T]CAGCCTCCCGAGTAG | 55632 |
rs111583823 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30600245 | GCTGAGGTCTAGCCT[C/G]CTCTGGAAAGTTTCC | 55632 |
rs111655933 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30583616 | TGGTGACTATAGTTG[A/G]TAACAATGTATTGTG | 55632 |
rs111659611 | in-del | -/TT | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30572721 | TAAGATATATTATCC[-/TT]TTTTTTTTAATTAAA | 55632 |
rs111683627 | snp | A/G | 0.0429648 | 0.14013 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575980 | TGCTATTCCTGTCAA[A/G]CTACCAACAACATTC | 55632 |
rs111683980 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30594137 | TGAGAGTCATCTTAC[A/G]TATCAAACCTTATTA | 55632 |
rs111788856 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30562866 | TCTCTCTCTCTGCCT[C/T]GGCTGCCAGGCAGGG | 55632 |
rs111862288 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30611690 | AGAGATAAGGTCTCA[A/G]TCTGTCACCCAGGCT | 55632 |
rs111894847 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30609886 | ACTGACTTATTGTCA[A/G]CCTTTCCTTCCTGTT | 55632 |
rs112013009 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | G2E3 | GRCh38.p7 | 14:30580287 | TCTTGGCTCACTGCA[A/G]CCTCCACCTCCCGAG | 55632 |
rs112042769 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | G2E3 | GRCh38.p7 | 14:30567683 | CTTCTGCTAGCTTTG[C/G]GTTTAGTTTGGTCTT | 55632 |
rs112058886 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30616160 | TGCCCAAAACAAATG[C/T]GGGAGTCTGTGCCTT | 55632 |
rs112307274 | snp | G/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30601954 | ATGATTTAAAAGTTT[G/T]TACCTATATCTCTAT | 55632 |
rs112313119 | snp | C/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30583405 | AATGGAGTCATAAAG[C/G]ACTAGTGAAGTAAGC | 55632 |
rs112554195 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607963 | GTGGTCCTTCACCTG[A/G]TTTCTTTTCTAAAAC | 55632 |
rs112634727 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | G2E3 | GRCh38.p7 | 14:30614276 | TTTATGCTGCTATAA[C/G]AATACCTGAGACTTG | 55632 |
rs112650655 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | G2E3 | GRCh38.p7 | 14:30615017 | AATTAGCTTTGAAGT[A/G]TAAAACACTTCAGAT | 55632 |
rs112690987 | in-del | -/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30594766 | CTAAAAGTAGTAAAG[-/T]TTGACTGATACCTTT | 55632 |
rs112708495 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620012 | ATCTGTGTTAAAACT[A/G]TGTATCCTCTAATGT | 55632 |
rs112717751 | snp | C/T | 3.10989e-05 | 0.00394316 | intron-variant | G2E3 | GRCh38.p7 | 14:30605848 | TGTATATACCAAATA[C/T]CACATGTATAGAAAA | 55632 |
rs112741912 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576229 | ACACATCTACAACCA[C/T]CTGATCTTTGACAAA | 55632 |
rs112816002 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30610873 | CATTGGAATGCAGCC[A/G]TGCCCATTTGCTACT | 55632 |
rs112875761 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576326 | AGCCATATGCAGAAG[A/G/T]TTGAAGCTGGACCCC | 55632 |
rs112891974 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30570187 | AATGAGAATTTGGCT[C/T]TTAATCTTATTGGGG | 55632 |
rs112895250 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616542 | GACATTAAAATGTTT[C/G]CTTGAACAAAGAGAA | 55632 |
rs112958695 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575756 | CAAATCAGAAAGGCA[A/T]TCCCATTCACAGTGG | 55632 |
rs112964724 | snp | C/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30591887 | ACTTTTTCATTTGGT[C/G]AGAATAGAGTGATCT | 55632 |
rs113211755 | snp | A/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30599247 | TGTTTGTTTGTTTTG[A/T]GATGGAGTCTTGCTC | 55632 |
rs113317388 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | G2E3 | GRCh38.p7 | 14:30611342 | TGAAAAACTTAGGAG[A/C]TTTCAGCAGAGATTT | 55632 |
rs113330893 | in-del | -/TA | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30593861 | GATGAAACTTTTTAA[-/TA]TGTATATTTATACTT | 55632 |
rs113358244 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559070 | GGCGGGAGCACACGG[A/G]CCCTTCCCCACAGCC | 55632 |
rs113366975 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30611000 | AGATGGCCCTCTGTT[C/T]TCGAGATAGAGTTGT | 55632 |
rs113421375 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562885 | TGCCAGGCAGGGAAG[A/G]GCCCCCTGTCCAGTG | 55632 |
rs113441398 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30565913 | ATGATCTGTCGCCTC[C/G]GCCTCCCAAAGTGCT | 55632 |
rs113488056 | in-del | -/G | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30580202 | AAAGGATTGTTTTTG[-/G]TTTTTTTTTGTTGTT | 55632 |
rs113504189 | snp | C/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30607865 | TAGAAGTGTATTTGA[C/T]ATATTTTCATCTGTA | 55632 |
rs113529795 | snp | A/T | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30615166 | ATCATGTGTAGTATA[A/T]CCATATCTTCTCTTT | 55632 |
rs113558453 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619758 | TATTTCCCCCCCTTT[C/T]AAAGACTGCCAGATT | 55632 |
rs113560222 | snp | A/G | 5.01299e-05 | 0.00500624 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605639 | ATGCATTCAGAAATC[A/G]AAACTTTAATCCTTC | 55632 |
rs113634547 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617255 | CAAAGACTCCATCTC[-/A]AAAAAAAAAAACAGA | 55632 |
rs113709529 | in-del | -/TGTG | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30573410 | AGAAACAACAGGATA[-/TGTG]TGTGTGTGTGTGTGT | 55632 |
rs113720438 | snp | C/T | 0.00108905 | 0.0233097 | intron-variant | G2E3 | GRCh38.p7 | 14:30592316 | CTATTTTCACATACT[C/T]TTCTAGAAATGCTGT | 55632 |
rs113814923 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30580923 | ACACCCCAGTTGAGA[A/G]CTACTGATCTTAGAT | 55632 |
rs113867286 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30615986 | CTTATAGTTGAAATT[G/T]TGTTTAGCTAGATTT | 55632 |
rs113896030 | snp | A/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30583406 | ATGGAGTCATAAAGC[A/G]CTAGTGAAGTAAGCT | 55632 |
rs113991464 | snp | C/G | 0.5 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30611841 | TTTTTTTCTTTAGAG[C/G]GGGGCTAGCTGTGTT | 55632 |
rs114054761 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30595089 | GTTGCGGTATGCTGA[A/G]ATAGCACCACTGCAC | 55632 |
rs114126634 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | G2E3 | GRCh38.p7 | 14:30566532 | TTAATTTCCTTTTTG[G/T]ATTGTTCATTGTTAT | 55632 |
rs114200467 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | G2E3 | GRCh38.p7 | 14:30584243 | TAATATTCCATCATA[G/T]GGGCATACCATATTT | 55632 |
rs114361202 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | G2E3 | GRCh38.p7 | 14:30563447 | TTATATCAGAGCTGC[A/G]TATCTGATGCAGGCT | 55632 |
rs114470233 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | G2E3 | GRCh38.p7 | 14:30572279 | TGAAAACAGTTTTAC[C/T]TCATCCTTCACAGTT | 55632 |
rs114508975 | snp | C/G | 0.0217236 | 0.101931 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617296 | TTTTCTGGAATCTAT[C/G]GACATTCCATGAGCT | 55632 |
rs114521880 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577431 | TTTCTGTTGATCAGG[G/T]ATTTGGGAGCTGCTT | 55632 |
rs114529513 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | G2E3 | GRCh38.p7 | 14:30597642 | AGGTAGCCATTTCAA[A/G]TGGTGAAATGCAAAA | 55632 |
rs114538527 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30575671 | CAACTTCAGCAAAGT[A/T]GCAGGATGCAAAATC | 55632 |
rs114652768 | snp | A/T | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618372 | ATATTTGTTTCTTTA[A/T]CCACCTTATTTTTAT | 55632 |
rs114693049 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30594122 | AAAATATTGGTTCTT[C/T]GAGAGTCATCTTACG | 55632 |
rs114694068 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30559729 | AGATGCTCTACGTGG[C/T]TCCGCGTTCCTCCTG | 55632 |
rs114818557 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | G2E3 | GRCh38.p7 | 14:30585576 | TTGTAAGTTTTTAAT[C/T]TTCTCCCCCTTTTTT | 55632 |
rs114820434 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30611152 | GCAGGGAAGTTTGAC[A/T]TGTTGTTTTTACTTA | 55632 |
rs114834794 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | G2E3 | GRCh38.p7 | 14:30569405 | TCAAACACAGAAAAT[A/G]TATAATTCAAGTGTA | 55632 |
rs114838253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591401 | TACATTTCAGTTAGC[A/G]GCACTGGTAGTATAT | 55632 |
rs114875259 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30583001 | CTAGTTTCCATAACT[A/G]GTAAACCCTGACATC | 55632 |
rs114904471 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30582636 | CTTGCGGGTAAAAGT[A/G]TAGGTATTGGGGATG | 55632 |
rs114950932 | snp | G/T | 0.0130921 | 0.0798413 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619589 | ATGAATTACTTGAAT[G/T]TATATTATCTGTGGT | 55632 |
rs114982182 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | G2E3 | GRCh38.p7 | 14:30590892 | CAAAATGCTTGGAAC[A/C]AGAATTTTAGATTTG | 55632 |
rs115242661 | snp | C/G/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30614607 | TTTCAACATGAGTTT[C/G/T]GAAGGAACTCATTTG | 55632 |
rs115334605 | snp | A/G | 0.02016 | 0.0983543 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618209 | CTTGAAATATTTAAG[A/G]ACATTAAACAAGACA | 55632 |
rs115352439 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | G2E3 | GRCh38.p7 | 14:30574585 | CCTCCCACCCTCCTG[C/T]GTCAGGTAGACCCCA | 55632 |
rs115382539 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | G2E3 | GRCh38.p7 | 14:30590217 | GGGAGCATTTTGGGT[A/G]ATGAAGGGATTCATC | 55632 |
rs115403832 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577404 | AAACAATAAACATTT[A/G]ATTACTGATAGTTTC | 55632 |
rs115405832 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | G2E3 | GRCh38.p7 | 14:30600125 | TTGTTATCACTGTTA[C/T]GTAGTCTTACTTAAC | 55632 |
rs115628699 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30582299 | AATAATAAATATAAT[C/G]AAATCAGGACAATTT | 55632 |
rs115812002 | snp | A/T | 1.68687e-05 | 0.00290414 | intron-variant | G2E3 | GRCh38.p7 | 14:30597570 | AAAAGATATTTTAAA[A/T]GTAGGATTTAATAGC | 55632 |
rs115816378 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30583731 | GCTGTTCCACAATAT[G/T]TACATATATCAAAAC | 55632 |
rs116009638 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563003 | CATTTGGGGCCACTA[C/T]CAGTCTCCGTGTCTT | 55632 |
rs116015295 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | G2E3 | GRCh38.p7 | 14:30573948 | TCTTGATCTTGAATT[C/T]TTTGGGAATGTTTTA | 55632 |
rs116061841 | snp | A/C | 0.0166325 | 0.0896639 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619972 | AGTTAGTGTCTGACA[A/C]CCAGGAACCTATAGA | 55632 |
rs116095728 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579452 | TATATGAGCAAAACT[A/G]TGTTTAAATCCAAAA | 55632 |
rs116112126 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | G2E3 | GRCh38.p7 | 14:30569266 | TGATCTCAGAAACTT[A/C]TGATCTTTCTGAATT | 55632 |
rs116288283 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | G2E3 | GRCh38.p7 | 14:30590390 | TAGCAGATAACAGAA[A/G]GGTAAATGTCATTAG | 55632 |
rs116369999 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30608423 | AGCAGATGAAAGTGC[A/T]CTTTGATGGAGGCCG | 55632 |
rs116429677 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30578513 | CAGGGCTTCTTACCA[A/G]ATGGAGTTACAGTAG | 55632 |
rs116594917 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30600933 | TTTTCATATGAACAC[A/C]GAGAGAACTGGACCT | 55632 |
rs116683723 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558357 | TCAGAGTTATTTAGC[A/G]CCCCTCACCCCCTAG | 55632 |
rs116809970 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | G2E3 | GRCh38.p7 | 14:30592243 | CAGATTCCCCACCAG[C/G]AGTATTTATTTATGT | 55632 |
rs116870572 | snp | C/T | 0.0421303 | 0.138889 | intron-variant | G2E3 | GRCh38.p7 | 14:30560861 | AGAAAATACTGTGAG[C/T]TTTCAAAACACTGAT | 55632 |
rs116872664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30591621 | GGCAGCATAACTCCA[A/G]TCTGTTTCTATCTTC | 55632 |
rs116972848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30583419 | GCACTAGTGAAGTAA[A/G]CTAGTCATGGAAAGA | 55632 |
rs117024700 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | G2E3 | GRCh38.p7 | 14:30593852 | AAATACTTCAGATGA[A/G]ACTTTTTAATGTATA | 55632 |
rs117213165 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30580377 | ACGCCCTGCTAACTT[A/T]GTATTTTTGGTAGAA | 55632 |
rs117309559 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | G2E3 | GRCh38.p7 | 14:30561098 | TACAAAGACCTTAAA[A/G]TAGTGTGTGCCACAT | 55632 |
rs117388740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563443 | GTATTTATATCAGAG[A/C]TGCATATCTGATGCA | 55632 |
rs117460979 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | G2E3 | GRCh38.p7 | 14:30598871 | TAGCCACATGTGGCT[A/G]TTGAGCACTTGAGAT | 55632 |
rs117594043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603954 | ACTCTTTCAAAATGT[A/G]AAGAATATCTGTTTT | 55632 |
rs117646989 | snp | C/T | 0.0182019 | 0.0936463 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559040 | CACCGAGCAGCAGCG[C/T]AGGAGCGCCAGAAGG | 55632 |
rs117678192 | snp | C/G | 0.0126979 | 0.078662 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557737 | ATATCAGATGCTAAA[C/G]TATCATAACTTACAT | 55632 |
rs117692199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30569355 | TAATAGGTAGGTATT[A/G]TCATCTCCATTGGAC | 55632 |
rs117794879 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30589077 | TCTTTTTTTCTTCCT[C/T]TAACCCACCTAACCA | 55632 |
rs117809156 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | G2E3 | GRCh38.p7 | 14:30580213 | TTTTGTTTTTTTTTG[G/T]TGTTGTTTTTGAGAT | 55632 |
rs117840204 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30587022 | GACCTATCATTATTT[C/T]GTGTTTGTTTGTTTG | 55632 |
rs117891151 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | G2E3 | GRCh38.p7 | 14:30592572 | TTAGATATAACATTA[C/T]ATGTATTACCCTCCC | 55632 |
rs117892551 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30581586 | GCATGCCTGTAATCC[C/T]AGCTACTCGCTAGGC | 55632 |
rs117968347 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30570073 | TGAAACATAGTTTTG[C/G]TGCAGATAGGATTCT | 55632 |
rs118095521 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30610889 | TGCCCATTTGCTACT[G/T]ATCTGACTGCTTTCA | 55632 |
rs118133605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574156 | TTCCCTTTTCTGAAC[C/T]GTTGGAGAGTAGGTT | 55632 |
rs137862853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30561166 | CTAAACTGTAAAAAC[C/T]GCATCACATACATTC | 55632 |
rs137864399 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30608775 | CTCCTACTTAAGCAT[A/G]TTCTATCCATTGTCT | 55632 |
rs137923929 | snp | C/T | 0.104149 | 0.203046 | intron-variant | G2E3 | GRCh38.p7 | 14:30604907 | ATTCATTCATTCATT[C/T]ATTTATGAGACGGAG | 55632 |
rs138039664 | in-del | -/TTCA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604873 | AGAGTTTGAGCTTGC[-/TTCA]TTCATTCATTCATTC | 55632 |
rs138080760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614399 | GAGCTGTCTTGCTGT[A/G]TCATAGCATTGTGGA | 55632 |
rs138085961 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30578210 | ATTAGGAAGGCTAAT[C/G]TGAACTGATCAAAAG | 55632 |
rs138252954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588235 | AGGAAAGGATTATTT[C/T]ACTTTTCTATAAAGT | 55632 |
rs138290102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563355 | CATGACCAGTAGGTA[G/T]GGTTGGTCTAAGGGA | 55632 |
rs138319087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30583596 | AAGAGATCTGTTGTA[C/T]AACATGGTGACTATA | 55632 |
rs138398240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30597193 | AAAAAATATATGGGT[A/G]ATGTAAAGCTAAGTA | 55632 |
rs138409159 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30567721 | TTTCTTTGGGCATAT[A/G]GTTGGGTCATTGTTT | 55632 |
rs138449529 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | G2E3 | GRCh38.p7 | 14:30594249 | CTTGAAAAAGATTCC[A/G]GTTATTAGTAACATC | 55632 |
rs138449922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30613830 | GAGAATTCCAGTTCT[C/T]AATGACACTGGAGAA | 55632 |
rs138482833 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30603865 | GTTTCAAGTTTAAAA[A/C]CTTAGAAGATAGTAA | 55632 |
rs138723068 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577290 | TGTTTATTTATTCAA[A/G]TGTTAGCCATCAGCT | 55632 |
rs138761436 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30582799 | ATACTTCGAGTTATG[A/T]CTTATCCCTTTAAAC | 55632 |
rs138778031 | in-del | -/TG | 0.210446 | 0.246851 | intron-variant | G2E3 | GRCh38.p7 | 14:30614242 | GATAACAGATAAACA[-/TG]TGTGTGTTCTTAGCT | 55632 |
rs138794995 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30579259 | TAGTACTCTAGACCT[A/G]CTTAACTCTAAAGCC | 55632 |
rs138811973 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30588916 | GTTAACTAGGGTTCA[A/G]TAGGTTTTCTTGTAA | 55632 |
rs138997321 | in-del | -/AATA | 0.0429648 | 0.14013 | intron-variant | G2E3 | GRCh38.p7 | 14:30581343 | TATGGTTCGTATCTC[-/AATA]AAACAGTTATTTAAA | 55632 |
rs139017664 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30563813 | CAACCTCCGCCTTCC[C/T]GGTTCCAGTGATTCT | 55632 |
rs139084218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585188 | GAAGTCCAATTATCA[C/T]TTTTTTCTTTTGTTA | 55632 |
rs139129318 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30565173 | TTATTATAGCTATTA[G/T]AGTGGACATGAAGTG | 55632 |
rs139166608 | snp | C/G | 0.00835141 | 0.0640778 | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559247 | AGTGGCACTGAGGCT[C/G]TGGAACTTCTGCCCA | 55632 |
rs139237356 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30571035 | TCTAAGAAATCTTAC[A/G]TAACATAAGGTCACA | 55632 |
rs139240788 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | G2E3 | GRCh38.p7 | 14:30599352 | CCTGCCTCAGCCTCC[C/T]GAGTAGTTGGGATTA | 55632 |
rs139279105 | snp | G/T | 0.00557734 | 0.0525397 | intron-variant | G2E3 | GRCh38.p7 | 14:30595189 | AAATATTAGAAATTC[G/T]GTTAATACTTGCAAA | 55632 |
rs139538534 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30591289 | ATCAGTGACCATTTT[A/T]ATTGCCGTCTTAAGG | 55632 |
rs139554593 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | G2E3 | GRCh38.p7 | 14:30604992 | ACCTCTGCTTCCCGG[A/G]TTCAAGTGATTCTCC | 55632 |
rs139585540 | snp | A/G | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593613 | CCTTGTTGTAAGAAC[A/G]CTTGGTTTCATAGAG | 55632 |
rs139629976 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30579553 | ATCAGTCTTCATAAA[A/G]TAATCTGTGTCCTAC | 55632 |
rs139744572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30609331 | ACCACCAGTCTCAAG[C/T]TAGCTAGTTCATAGT | 55632 |
rs139809699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605331 | AAACTAAGATTATCA[A/C]ATAACTGTTTTTGGT | 55632 |
rs139829218 | snp | A/G | 3.2962e-05 | 0.00405954 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601787 | AATGGGAAATAAAGC[A/G]CTGTCAGTGTTGTGG | 55632 |
rs139869782 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | G2E3 | GRCh38.p7 | 14:30562496 | TTGTTCTAGCGGTAA[C/T]ACCAGCGTCTGGGAA | 55632 |
rs139995925 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | G2E3 | GRCh38.p7 | 14:30594617 | AGAATGGCATGAACC[C/T]GGAAGACGGAGCTTG | 55632 |
rs140045685 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30573093 | CTGCTTCAGCCTTTC[A/G]AGTAGCTGGGACTAC | 55632 |
rs140104715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30616208 | TTTGGAGAAGAATCT[A/G]TGATGATAGCAATAT | 55632 |
rs140109291 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620351 | CTCATAGTCTTGGGA[A/G]AGAATCTGTGATGGA | 55632 |
rs140166042 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30589311 | TATTAGACTGAATAG[G/T]ATGGATATATATTTT | 55632 |
rs140390861 | snp | A/C | 0.00389476 | 0.0439569 | intron-variant | G2E3 | GRCh38.p7 | 14:30592298 | TTTTTTATGTTGTGA[A/C]CCCTATTTTCACATA | 55632 |
rs140457966 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30587399 | TAAGATATTAGTGGC[A/T]CATTACCACCTTAGC | 55632 |
rs140521005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563270 | TCCGTTTGATCACTT[A/C]AGACAGTTGCCTAAT | 55632 |
rs140527988 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30607645 | ACCAAAGTGTTCACA[A/G]TGGTTATTATGGTGG | 55632 |
rs140574601 | snp | C/G | 6.64231e-05 | 0.00576256 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612339 | GTAAAAGACATACTT[C/G]GCTACCATGTAATTC | 55632 |
rs140609202 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | G2E3 | GRCh38.p7 | 14:30568697 | ATCTCATCCTTCTTC[C/T]TAAATGTTATTGTGT | 55632 |
rs140663699 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30613356 | CATAGATTTAAATAT[A/G]TTTGATGTGTTTAAA | 55632 |
rs140708807 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30572308 | TTTTGTCTTCTTTTC[C/T]CTTGGAGTACACTGT | 55632 |
rs140744473 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30566999 | GGTTGATTTCCATAT[G/T]CTGAACCACCTTTGC | 55632 |
rs140801763 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | G2E3 | GRCh38.p7 | 14:30606254 | TTTTTTTTTTTGCAC[A/G]ATTATGTATATGATG | 55632 |
rs140838546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582385 | ACTTATAAAAATGCA[C/T]GCCTGAAACCTAGTC | 55632 |
rs140906681 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30595764 | GTCTTATCCAATCTA[A/G]ATAGCTGTATGTGGT | 55632 |
rs141018669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566561 | ATATAGAAATACAAC[A/T]GATATTTGTGTGTTG | 55632 |
rs141220050 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | G2E3 | GRCh38.p7 | 14:30564839 | ATTCTATGGATATAC[C/T]ACATTTTGTATATCC | 55632 |
rs141277424 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30581371 | TTTAAAGGAAAAAAT[G/T]CAGATGAGAACAATT | 55632 |
rs141357590 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30611891 | TTCTGGCCTCAAGCA[A/G]GCCTCCCACCTCAGC | 55632 |
rs141383208 | in-del | -/TGTGTGTGTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563696 | TAACTTTGTTACTTT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 55632 |
rs141411430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615328 | GTATGAATGTTGGCT[C/T]ATTATTTTTCTTCTC | 55632 |
rs141455005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30608563 | CAAAGGGAAACAAGT[A/G]GTAGGGATCGGGGAG | 55632 |
rs141483611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593263 | CTGTATAAGTAAGTC[A/T]CACTACCAGAAAAGT | 55632 |
rs141517652 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30604313 | AAAAAGCAAAACCTG[G/T]CCTACACTAGGGCAC | 55632 |
rs141556887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30598749 | CTAATGCACATTTAC[A/G]TCTGTTTACAGAGAA | 55632 |
rs141561719 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | G2E3 | GRCh38.p7 | 14:30596200 | CCTGGAATCCTCTTT[A/G]TTAGCTTCTCTCTTC | 55632 |
rs141592232 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | G2E3 | GRCh38.p7 | 14:30598150 | CTCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 55632 |
rs141616576 | in-del | -/AC | 0.0333695 | 0.124785 | intron-variant | G2E3 | GRCh38.p7 | 14:30572269 | TGATCATATGTGAAA[-/AC]AGTTTTACTTCATCC | 55632 |
rs141688760 | in-del | -/CGTTTATATGTCAGCCTATTTCC | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619727 | ATTATGCTAGGTGAT[-/CGTTTATATGTCAGCCTATTTCC]CCCCCTTTTAAAGAC | 55632 |
rs141718619 | snp | C/T | 0.000183045 | 0.00956499 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592391 | ATGTAAACGAAGTTA[C/T]CATTTCCCATGTGGA | 55632 |
rs141849560 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30588732 | TTCCAGAAGTTTCAG[C/G]AGAGCCTGGCTTGCA | 55632 |
rs141905028 | in-del | -/CCGGC | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30568849 | AGTGCAATAATACTA[-/CCGGC]CTGGCTTTTATATTT | 55632 |
rs141911792 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | G2E3 | GRCh38.p7 | 14:30580555 | GGCATGGCTATTGAT[G/T]ATGTGATTTTTCTTT | 55632 |
rs141915297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582888 | TTATTTCTTTTCAGT[C/T]CTAGAATCTATTTGG | 55632 |
rs141973775 | snp | C/T | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577061 | GAAACCCCGTCTGTA[C/T]TAAAAATACAAAAAT | 55632 |
rs142022341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560652 | ATATCCTAATCTCTT[C/T]ATTTTTTTCTACCTG | 55632 |
rs142196586 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562980 | CAATAAATATCAGCA[C/T]AGCCTGGCATTTGGG | 55632 |
rs142200360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600340 | TTACAATATAGTTGG[C/T]GTTATTTAAATTTAA | 55632 |
rs142227251 | in-del | -/TTTATA | 0.0228947 | 0.104514 | intron-variant | G2E3 | GRCh38.p7 | 14:30607222 | GCATAAGTCAAACTT[-/TTTATA]TTTATATACACAAAG | 55632 |
rs142309400 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30563826 | CCCGGTTCCAGTGAT[C/T]CTCCTGCCTCAACCT | 55632 |
rs142310689 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | G2E3 | GRCh38.p7 | 14:30606547 | TAAAAATAAAGAAAA[A/G]ACTTTCCAAATAGTA | 55632 |
rs142475306 | snp | C/T | 0.000727164 | 0.019054 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602104 | TACCCAGACAGTCAC[C/T]TGGATCCCAGAGTAA | 55632 |
rs142484814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30601613 | TTTTTACATTAGAGA[C/T]ATTTAGAGAAGCAGA | 55632 |
rs142496999 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30597248 | TGGAAAAAAGAATTA[A/T]AGATTTTAGCAGTGG | 55632 |
rs142510288 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576523 | AAATTGACAAGTGGG[A/G]TCTAGTTAAACTTAA | 55632 |
rs142512495 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30590834 | AAGGTGGTCTCTAAA[A/G]GTCCCCTTATGGTTT | 55632 |
rs142815152 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30574749 | GTTCCTGCAAAAGAC[A/G]TGATCTTACTCTTTT | 55632 |
rs142851760 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30566530 | ACTTAATTTCCTTTT[C/T]GGATTGTTCATTGTT | 55632 |
rs142910588 | snp | G/T | 0.0872718 | 0.189788 | intron-variant | G2E3 | GRCh38.p7 | 14:30611596 | TCTCAGCTGTTACTC[G/T]TTTTCATGAATTCTC | 55632 |
rs142927182 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30569075 | TTTTAAGAAACTTTT[C/T]ATTGAGGTATAATAT | 55632 |
rs143054531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608940 | TGAGCTGAGCTCACA[A/C]CACTGCACTCCAACC | 55632 |
rs143107321 | snp | A/G | 8.2373e-05 | 0.00641714 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598536 | AGCTTCTGCAGCACT[A/G]TGAGCGTTGTGATGT | 55632 |
rs143136553 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30586950 | TATCTCTAAAAATAG[A/T]CATTTTGTTTTTTGA | 55632 |
rs143256459 | snp | C/T | 0.000505238 | 0.015886 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612362 | TGTAATTCAGAGAGT[C/T]CACACACCCTTTGAA | 55632 |
rs143257941 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30592850 | AATTTGATTGAGTAC[A/G]CAAAGTAAATATTAT | 55632 |
rs143307581 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595078 | GGGAGGTAGAGGTTG[C/T]GGTATGCTGAGATAG | 55632 |
rs143363903 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30597786 | GATTGACTTTGTACA[C/G]TTATAATAGGCTTCA | 55632 |
rs143375316 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30591809 | ACATTCACAGGTACT[A/G]GGAGTCGGGACCTGA | 55632 |
rs143483472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567903 | GTCATTGGAGAGGAT[A/G]TTTTGTGTGATTTCA | 55632 |
rs143577824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573623 | TATAGGTTCCAGTCC[A/G]GATCTGAAGGCCTGA | 55632 |
rs143589981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568326 | TAGCTTGACCCTAGT[A/T]GATAGTGTATGTATG | 55632 |
rs143654861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615096 | AGCCAAATAATGTAG[A/G]TACATAAAATATTCA | 55632 |
rs143704815 | in-del | -/AT | 0.029116 | 0.117091 | intron-variant | G2E3 | GRCh38.p7 | 14:30564719 | ACCTAGTTCCAAAAC[-/AT]GTAACCTTTTATGTC | 55632 |
rs143734676 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575933 | AATATCATTAAAATG[A/G]CTATTGTGCCCAAAA | 55632 |
rs143767529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609382 | ATCCATGTCCAAAGG[C/G]CTTTTCTAATTTTTC | 55632 |
rs143769801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30560279 | TATTAAAAATCGTCA[A/G]TTTTGTGTAGCTTAA | 55632 |
rs143793032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30571585 | TGTGATCCAATTTGA[A/G]TTAAGTTTTAATATA | 55632 |
rs143804746 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30603109 | TAGGCGGGCGGATCC[C/T]GAGGTCAAGAGATCG | 55632 |
rs143807307 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617097 | CTGATTTATATTAAG[A/G]TGACCCACACTGCAA | 55632 |
rs143897025 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | G2E3 | GRCh38.p7 | 14:30578099 | TGTGAATAGTACTTA[-/T]TTTTTTTTACTAAGG | 55632 |
rs144014855 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | G2E3 | GRCh38.p7 | 14:30594411 | TTAAAAGATGTAGGC[C/T]GGGTGTGGTGGCTCA | 55632 |
rs144065087 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599568 | TCCATATATAGTCAC[C/G]TTCTGATGTACTAGG | 55632 |
rs144100998 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595458 | CATACTTGACCTAGT[A/G]TCATTAAGGCCTTTT | 55632 |
rs144133112 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | G2E3 | GRCh38.p7 | 14:30589819 | CCACTCTGCTGTTCT[C/T]TAAACCTTTGATCCT | 55632 |
rs144198631 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30584982 | GATTACAGGCACACA[C/T]CACCATGCCCAGCTA | 55632 |
rs144208076 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30580652 | GACATAGGAGTTGTA[A/G]TTCTGCAAATATAAT | 55632 |
rs144225090 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30579035 | TTAAAATGATGTTCT[A/G]TAGATTGTGATCCTC | 55632 |
rs144330682 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | G2E3 | GRCh38.p7 | 14:30583839 | TTCAAGTTGTATTTT[C/T]GTGTGTGTTGGGAGG | 55632 |
rs144514890 | in-del | -/CAG | 0.0425829 | 0.139564 | intron-variant | G2E3 | GRCh38.p7 | 14:30611349 | CTTAGGAGATTTCAG[-/CAG]AGATTTTGAATGAAT | 55632 |
rs144575247 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30574919 | ATGGTAGAATGATTT[A/G]TAGTCCTCTGGCTAT | 55632 |
rs144579720 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | G2E3 | GRCh38.p7 | 14:30605150 | ATCCGCCTGCCTCTG[C/T]CTCCCAAAGTGCTGG | 55632 |
rs144593195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567382 | TATTTCTTCTTGTCA[C/T]TTTTGTTATTTGTTT | 55632 |
rs144671965 | in-del | -/GTAAATCATTATGATAG | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617931 | AGTTTTCCATGAAAG[-/GTAAATCATTATGATAG]TAAATCATTATGGGA | 55632 |
rs144959470 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | G2E3 | GRCh38.p7 | 14:30586110 | GCAGAGGCTCCAGCC[C/G]TGAGAAAGTTCTGAG | 55632 |
rs145113929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566803 | AAAGTGTGCAGTCTT[G/T]CACTGATAATTATGT | 55632 |
rs145145782 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563736 | GTGTGTGTGTGTGTG[A/T]GTGATATAGAGTCTC | 55632 |
rs145146876 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | G2E3 | GRCh38.p7 | 14:30613051 | AATACATATATTGAC[C/G/T]GTTCTTTGATTAACA | 55632 |
rs145223618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30608593 | GGACTTAATGCGTCC[A/G]CCTAAAAATAGTTCA | 55632 |
rs145225517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571439 | TAACTATGTTTTTTT[G/T]ATTAGAAAGTTCTTA | 55632 |
rs145349084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605393 | GGGAATTGGGGAAGA[A/G]TATCCTATTAATCTT | 55632 |
rs145352220 | snp | C/G/T | 0.0001322 | 0.00812919 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602056 | ATAATGTGGGGATTA[C/G/T]AGATTGTTTGTTGGA | 55632 |
rs145355964 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600666 | GACAAAGATATTGTC[C/T]ATCTGAATGACTGCT | 55632 |
rs145387183 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576405 | GATGTAAAACCCAAA[A/T]CTATAAAAACCCTGG | 55632 |
rs145527124 | snp | A/G | 0.00396942 | 0.0443729 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592422 | CTTCAGAGAGAATGT[A/G]TTTTCCAGTTTACTG | 55632 |
rs145628573 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30587692 | TTTCTCCTAGCTAGC[A/G]TCAGGAAACCTCAGC | 55632 |
rs145726272 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30595965 | TGGTATCTTCCATGT[A/G]TCTTATCCTGTTTTT | 55632 |
rs145741526 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30611086 | TTAGCATTATTGTTT[G/T]CATCCACATGGTTGA | 55632 |
rs145839747 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577094 | GCTAGGCGTGGTGGC[A/G]TATGCCTGTAGTCCC | 55632 |
rs145865276 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572859 | GATAAAATTGAGGCT[A/G]AGGTCTCAGGAAAAA | 55632 |
rs145924608 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574136 | ATTGTACATTTGCAT[C/G]TAACTTCCCTTTTCT | 55632 |
rs145951353 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | G2E3 | GRCh38.p7 | 14:30563880 | CCTGCCACCACGCCC[A/G]GCTAATTTTTGTGAT | 55632 |
rs145955146 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30562217 | AGAGACTGGGGGCAC[A/G]AGCTGTTCCAGTATA | 55632 |
rs146097871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30616044 | TCTGTATTTGTTATA[C/T]ACAATAAGTAGTTGT | 55632 |
rs146200299 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30598820 | TCTTATCACGAGACT[A/G]TTTTCTAGAGCCACA | 55632 |
rs146209274 | in-del | -/CCCCCC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580161 | TCCTGGCAAATGCAA[-/CCCCCC]CAGCCACAAATACGG | 55632 |
rs146218891 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30595099 | GCTGAGATAGCACCA[C/T]TGCACTCCTGTCTGG | 55632 |
rs146315397 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30583404 | AAATGGAGTCATAAA[A/G]CACTAGTGAAGTAAG | 55632 |
rs146318058 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30579490 | TACAGTCAGTATGAA[A/T]TATAAATTCTAATTG | 55632 |
rs146347278 | in-del | -/C | 0.0444908 | 0.142359 | intron-variant | G2E3 | GRCh38.p7 | 14:30590332 | TTTAGACTTTGTTTT[-/C]CACAGATGCCAAAGT | 55632 |
rs146633967 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30608221 | TGGAGTTCTGAACCA[C/G]TTAAAAGATAGTTTT | 55632 |
rs146697386 | snp | C/T | 0.000494168 | 0.0157111 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612371 | GAGAGTCCACACACC[C/T]TTTGAAAGGTAAGTT | 55632 |
rs146735236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30591972 | TGCCTAATTTATGTG[C/T]TTTCTCTTGAGATTT | 55632 |
rs146754001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587303 | TCAGAAGAAAGCAAA[C/T]GAGTGATTTCATACT | 55632 |
rs146855581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571758 | TTTCCCTTGTGTTCT[A/G]TTGAGCTATATATCT | 55632 |
rs146874834 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | G2E3 | GRCh38.p7 | 14:30566970 | TTTTCTCTATTAGTA[C/T]GGTATATTATATTGG | 55632 |
rs146879016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30613128 | AGTTAGACAACTTAT[A/G]TATCTCCTTACACTC | 55632 |
rs146950345 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620549 | TTCCTTCAAAATATT[A/G]GTAATAGTACTGAAG | 55632 |
rs146979921 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30614342 | TTCTGGAGGCTGGGA[A/G]GTCCAAAGGCATAGT | 55632 |
rs147054846 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30597185 | AAGATTGAAAAAAAT[A/T]TATGGGTGATGTAAA | 55632 |
rs147203713 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | G2E3 | GRCh38.p7 | 14:30568374 | TTCTGTCAACCTTTG[C/T]CTTTTAATTGGAGCG | 55632 |
rs147207250 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30615152 | ATGGATTTGAAAGTA[C/T]CATGTGTAGTATATC | 55632 |
rs147207412 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30565912 | CATGATCTGTCGCCT[C/T]GGCCTCCCAAAGTGC | 55632 |
rs147223596 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | G2E3 | GRCh38.p7 | 14:30609669 | AGACCTGGGTCTTGC[A/T]AGCACATTGAGTCTA | 55632 |
rs147313487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594442 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 55632 |
rs147329960 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30589851 | AGTCAACCCAACCAT[A/T]TACTTTTTTATTCTT | 55632 |
rs147417305 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30609143 | TACAGTGTATTACAA[C/T]AATTCTGTTTATTTG | 55632 |
rs147522342 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | G2E3 | GRCh38.p7 | 14:30589012 | CTGAATTGTCTCCAT[C/G]TGTATTCACCACTCC | 55632 |
rs147525085 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30584776 | TTTAATGCATCCTGG[C/T]TACTAGACCTTTAGA | 55632 |
rs147645477 | snp | C/G | 0.0872718 | 0.189788 | intron-variant | G2E3 | GRCh38.p7 | 14:30562886 | GCCAGGCAGGGAAGG[C/G]CCCCCTGTCCAGTGG | 55632 |
rs147650086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578779 | AGGTTGAACTGTAGA[G/T]AAGTCCTTTAAGAGG | 55632 |
rs147675008 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30606158 | TTGTATATTTGGAAT[C/T]TGCGGTTAACATAGA | 55632 |
rs147691179 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601124 | TTGCCACTCACACAC[A/T]CGGGGAGCTAAATCT | 55632 |
rs147737745 | snp | A/C | 0.00130373 | 0.0254983 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602082 | TTGGAAGAGTCATCA[A/C]CTAAATTACCCAGAC | 55632 |
rs147778881 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30585049 | CCATGTTGGGCAGGC[C/T]GGTCTCGAACTCCTG | 55632 |
rs147795261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580772 | TCTAGACTATCGTTT[C/G]TTGTGTAGGACTGTT | 55632 |
rs147861236 | in-del | -/TAACT | 0.0425829 | 0.139564 | intron-variant | G2E3 | GRCh38.p7 | 14:30612516 | GCTATTTTTAAATAA[-/TAACT]TAAGCCTTTTTAGGA | 55632 |
rs147883763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566195 | GAATTGGAAAATTTG[A/C]ATCCTCCAACTTTTT | 55632 |
rs147893280 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30563249 | AAAAAACAAAACTTT[A/T]CTTTTTCCGTTTGAT | 55632 |
rs147962269 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30580310 | CTCCCGAGTTCAAGC[A/G]ATTCTCTTGCCTCAG | 55632 |
rs148009150 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30567924 | TGTGATTTCAGTCTT[A/G]TAAAATGTATTATTT | 55632 |
rs148042892 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30582180 | TTGATACTTTTTCCT[A/G]AGATGGACTGTTTCT | 55632 |
rs148066743 | snp | C/T | 0.000170573 | 0.00923349 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586761 | CTGTCCTAATAAATA[C/T]GGAGAAAAGAAAACT | 55632 |
rs148219086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564745 | TATGTCTGACTTCCC[A/T]CATTTAATATAATGT | 55632 |
rs148222622 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | G2E3 | GRCh38.p7 | 14:30608946 | GAGCTCACACCACTG[C/T]ACTCCAACCTGGGCA | 55632 |
rs148276141 | snp | A/G | 0.00131917 | 0.0256485 | intron-variant | G2E3 | GRCh38.p7 | 14:30615325 | CATGTATGAATGTTG[A/G]CTCATTATTTTTCTT | 55632 |
rs148376229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597956 | ATAAAAAATTTCTTG[C/T]TAACTTTTCATTTAG | 55632 |
rs148388996 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558327 | TGGTGGCAACATCAA[C/T]CACAGCCATAAAGGT | 55632 |
rs148395548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30590264 | AATGAAGGACACTGA[C/T]ACATTATAGTTGAAG | 55632 |
rs148435440 | in-del | -/TGC | 0.11228 | 0.208646 | intron-variant | G2E3 | GRCh38.p7 | 14:30604582 | CAAGTTCTGGGGTAA[-/TGC]TGCTGCTGCTGCTGC | 55632 |
rs148632856 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30595052 | CGGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 55632 |
rs148754501 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30571541 | CATGAAGATTCTTCA[C/T]TATGTTTTCTTCTAG | 55632 |
rs148762336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583958 | CCATCACCACTATCT[A/G]GTTCTAAAACATTTT | 55632 |
rs148801046 | snp | C/T | 3.30262e-05 | 0.0040635 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602083 | TGGAAGAGTCATCAC[C/T]TAAATTACCCAGACA | 55632 |
rs148950384 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30566320 | AATTGTATCAAATCC[A/T]TAAATTGCTTTGGGG | 55632 |
rs148969508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560015 | CTGCCTTTTCGCCTC[A/C]CTCATTCATTGGCCA | 55632 |
rs148985544 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30602967 | AATGGCAGGAGTCTA[A/C]ATGTCAGCTCTTCCC | 55632 |
rs149000182 | in-del | -/A | 0.0456462 | 0.144012 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576837 | TAAAAATGCTAGATT[-/A]AAAAAATCAATCAAT | 55632 |
rs149019193 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619066 | TTTAAACACTTTCCA[A/G]TATGGAAACTTTAAC | 55632 |
rs149073755 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30586225 | AGGTCCATTTTACCC[C/G]CTCTTGGACCAGTAA | 55632 |
rs149230135 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576462 | GACATAAGAATGGGC[A/G]AAGATTTCATGACAA | 55632 |
rs149249211 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30567778 | AGTATTTTCTAATTT[C/T]CCTTGTGATTTCTTT | 55632 |
rs149298346 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30605050 | TACAGGCATACGCCA[C/G/T]GACGCCCAGCTTATT | 55632 |
rs149400823 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30588929 | CAATAGGTTTTCTTG[C/T]AAATAATGCCTTAAT | 55632 |
rs149463072 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30608854 | AGGCGTGGTGGCATG[C/T]GCCTGTAATCCCAGC | 55632 |
rs149543567 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30578270 | CAACTTTTAGGTAAT[A/T]TGATACTGCTATAAT | 55632 |
rs149596446 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583673 | ATTCTCACCACAAGT[C/G]GTAAATATGTGAAGT | 55632 |
rs149716367 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30562687 | GCCCACCCGCAGTTA[C/G]CTGGAGGCCTAACCG | 55632 |
rs149765880 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | G2E3 | GRCh38.p7 | 14:30595906 | TACAGAATTGTCACT[A/G]TTTTTGTTCAGCTTG | 55632 |
rs149773574 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | G2E3 | GRCh38.p7 | 14:30610489 | GGTGTGGTGGCGCGC[A/G]CCTATAGTCCCAGCT | 55632 |
rs149841976 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30580300 | CAACCTCCACCTCCC[A/G]AGTTCAAGCAATTCT | 55632 |
rs149895551 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30585474 | TTGACCATAGATGTA[C/T]ATATTTATTTCTGGA | 55632 |
rs149936895 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | G2E3 | GRCh38.p7 | 14:30565822 | ACCCACCACCACACC[C/T]GGCTAATTTTTTTGT | 55632 |
rs149983595 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30571061 | TCACAGAAATTTTCT[C/T]CTCTGTGTTTTTTCT | 55632 |
rs150045841 | in-del | -/AGA | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30600710 | CCTCTCATCCTAGTG[-/AGA]AGAAGAAGGCAGTTT | 55632 |
rs150098765 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613601 | AGTCTGGATGCTAGA[G/T]ATTCTTAGTTTTGGT | 55632 |
rs150159904 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | G2E3 | GRCh38.p7 | 14:30582505 | AGATGTACCTCCATC[C/T]AGGGTTCATGGCAAG | 55632 |
rs150194022 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562997 | GCCTGGCATTTGGGG[C/T]CACTACCAGTCTCCG | 55632 |
rs150239900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602840 | TGGTCTTGAACTCCT[G/T]GTCTCAAGTAGTCCT | 55632 |
rs150300249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30573164 | AGATATGTTTATTAT[C/T]TCCTAGAATGTAAAT | 55632 |
rs150356974 | in-del | -/GTAAATCATTATGATAG | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617930 | CAGTTTTCCATGAAA[-/GTAAATCATTATGATAG]GTAAATCATTATGGG | 55632 |
rs150360562 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577636 | ATGTTGAAAATTTTT[A/G]TGACATGGCAGCTGG | 55632 |
rs150402278 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558180 | GCCTACCAAAGTGCT[A/G]GGATTACAGGCGTGA | 55632 |
rs150436975 | in-del | -/GTA | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557900 | TAAACCTTTCAAACT[-/GTA]TTTTTTTTTTTTTTT | 55632 |
rs150466307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30608205 | TATTTCTGTTTACCA[A/G]TGGAGTTCTGAACCA | 55632 |
rs150539878 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30604969 | TGGCGTGATCTTGGC[A/T]CAACGCAACCTCTGC | 55632 |
rs150599727 | in-del | -/GTGTGTGTGC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573423 | TATGTGTGTGTGTGT[-/GTGTGTGTGC]GTGTGTGTGTGTCTC | 55632 |
rs150679930 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579890 | ATTGTACTTAAATCT[C/G]ATTAACATTTCTAGT | 55632 |
rs150714166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561026 | TCATTTCCCTCTACC[G/T]TATGATGAGGTTACC | 55632 |
rs150767792 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30564854 | CACATTTTGTATATC[C/G]ATTCATCAATTGATG | 55632 |
rs150801701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569819 | CAAATGGCAGAATCA[G/T]CAAGAGCAACTTCCA | 55632 |
rs150831497 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615455 | AGTCTTTCTGCAAAA[A/G]TCCTTAGTGAGCTTT | 55632 |
rs150934449 | in-del | -/T | 0.0865458 | 0.189163 | intron-variant | G2E3 | GRCh38.p7 | 14:30605413 | AATATCCTATTAATC[-/T]TTTTTTCCCCTCGTC | 55632 |
rs150939228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576747 | ACATCGAATAATGCA[A/G]TGCATAGACTAAGTT | 55632 |
rs150947250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30590871 | ACAGATTGAATATCC[C/G]TTATCCAAAATGCTT | 55632 |
rs151007162 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | G2E3 | GRCh38.p7 | 14:30595716 | AATAACTTTTGTACT[C/G]TGGTATCGGTCTTAA | 55632 |
rs151068192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566555 | ATTGTTATATAGAAA[G/T]ACAACTGATATTTGT | 55632 |
rs151152476 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619834 | ATGTGTTTATGCCAC[A/T]AAAGGTAAACTGCCT | 55632 |
rs151227732 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30600341 | TACAATATAGTTGGC[A/G]TTATTTAAATTTAAT | 55632 |
rs151280805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607532 | GTATAACATCACTAG[A/G]TCATAGGAGTTTTTC | 55632 |
rs151294449 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605706 | TAATTTTGGAAGTGA[A/G]CATCCTGGATCAAAG | 55632 |
rs180691075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30596739 | AGAATTCCTTGAAGT[C/T]GAAGCTGTCATGTTT | 55632 |
rs180718261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30609815 | CAAGCTGTCTTGGAG[A/G]GTCATTTTCATACTC | 55632 |
rs180722118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30583948 | TGTTGTGAAACCATC[A/G]CCACTATCTAGTTCT | 55632 |
rs180891655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30562357 | TAATAATCCTCGCTC[C/T]ACAATCATAACCTAG | 55632 |
rs180938403 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602138 | TCTACTGAGGTATGT[A/G]TTTTGAATTGGAGAA | 55632 |
rs180944525 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579122 | TCAAAAGCGCCATCG[C/T]ATACCTGTAGAGAAT | 55632 |
rs181116529 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588739 | AGTTTCAGCAGAGCC[A/T]GGCTTGCAAGCCAGG | 55632 |
rs181128376 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570585 | TGTCTTCAAGTTCGC[C/T]GATTCTTTCTCCTGC | 55632 |
rs181190131 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30579898 | TAAATCTCATTAACA[C/T]TTCTAGTAGGCTGTT | 55632 |
rs181197180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615743 | AGAGTAAATTTATAT[G/T]TTGTAATTTTTTTCT | 55632 |
rs181340605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562898 | AGGGCCCCCTGTCCA[C/G]TGGACACGTGACCCA | 55632 |
rs181340784 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30603156 | TATGGTGAAACCCCG[C/T]CTCTATTAAAAATAC | 55632 |
rs181382366 | snp | A/G | 0.000315762 | 0.0125611 | intron-variant | G2E3 | GRCh38.p7 | 14:30616243 | CATGGATTTACTTTT[A/G]TTTCTTTTACTCTTT | 55632 |
rs181395903 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | G2E3 | GRCh38.p7 | 14:30590594 | GTCTACAAGGGAAGC[A/G]CATAAGAAACATTTA | 55632 |
rs181402615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571092 | AGAAATTTTATAGTT[C/T]TACATTTTGTATTTA | 55632 |
rs181419118 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30566993 | TATATTGGTTGATTT[C/G]CATATGCTGAACCAC | 55632 |
rs181567907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30567355 | CTTGTTTGTAGATTT[A/G]TTGAAATTTTCTATT | 55632 |
rs181604102 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594834 | GATTATTCAGTTAAA[A/C]GTGCAGGATGAAGGC | 55632 |
rs181611691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574671 | ACAAGTGAGAACATG[C/T]GGTATTTGGTTTTTT | 55632 |
rs181793189 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30584958 | TTCCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA | 55632 |
rs181867023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607480 | GTAAGTATATGTATA[C/T]CTAAATATACAAAAG | 55632 |
rs181873175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30583643 | TGTGTACTTGAAAAT[C/T]AGTAAATTTTAAGTA | 55632 |
rs181899877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566508 | GCTATTGTAAATGGA[A/G]TTGTTTACTTAATTT | 55632 |
rs182009958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576081 | TCCTAAGCAAAAAGA[A/G]CAAAGCTGGAGGCAT | 55632 |
rs182042182 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30610689 | GGAGTATATACAAGT[A/T]AGGTTTTAGGCTAAA | 55632 |
rs182119066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576429 | ACCCTGGAAGACAAC[C/T]TAGGCATTATCATCC | 55632 |
rs182142097 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558585 | AACACCATCAAATAG[C/T]TTATTTGAGACCAGG | 55632 |
rs182243880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564372 | ACAAGATCTCTGTCA[C/T]CCAAAGCTGGAGCTC | 55632 |
rs182247789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561951 | TTTATAAACTATGGA[A/G]AAATAAGTATTGAAA | 55632 |
rs182272895 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600784 | CTAGATAAACTGAAA[C/T]GGAATCCTCACTCTG | 55632 |
rs182291003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595681 | GCTAATTCTTGAGTC[A/C]CTCTCTCTAAAGGAG | 55632 |
rs182308921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30605251 | AATTTGAGATAATTA[C/T]CTATCAACTTTCTTG | 55632 |
rs182316616 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581689 | CCTAAGTGACAGAGC[A/G]AGACCCTGTATCAAA | 55632 |
rs182348530 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30611496 | CTAACCTGTATGAAA[G/T]TGTCTTGCACATAAA | 55632 |
rs182376936 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558024 | TTCACACCATTCTCC[A/T]GCCTCAGCCTCCCGA | 55632 |
rs182451169 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | G2E3 | GRCh38.p7 | 14:30567908 | TGGAGAGGATATTTT[C/G]TGTGATTTCAGTCTT | 55632 |
rs182559099 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30578594 | CACTACATTTTGTGG[C/T]GTCTAGGTTGGATGA | 55632 |
rs182612186 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30585837 | CTTGCATGAGCCTAA[A/G]CATCAGCCAGAGGTG | 55632 |
rs182629064 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30591581 | TCACATGGCTGCTGG[A/C]AACCTTTGGAGTACC | 55632 |
rs182650629 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618268 | TCTCACCAATAGTAA[C/T]TGAAAGATCAATTAT | 55632 |
rs182660559 | snp | A/G/T | 0.000795037 | 0.0199223 | intron-variant | G2E3 | GRCh38.p7 | 14:30592281 | ATATTATAATACTCA[A/G/T]ATTTTTTATGTTGTG | 55632 |
rs182668299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571893 | AATGTTTTTGCTATT[A/G]CAAGACTTTTGCATT | 55632 |
rs182770141 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30564103 | TATACAATTTGTATG[C/G]AATAAAAGTCACCCA | 55632 |
rs182912336 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30571653 | CATTCAGTTATTTCA[A/G]TACTATTTATTGAAT | 55632 |
rs182938411 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618516 | ATACTTTGTTGGGGT[C/G]GGGGTGGCAGGTGGA | 55632 |
rs182999878 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617478 | TTTTAGATATTTGAA[C/T]GATCTCTGTGGATTG | 55632 |
rs183139663 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | G2E3 | GRCh38.p7 | 14:30612509 | TTTAAATGCTATTTT[A/T]AAATAATAACTTAAG | 55632 |
rs183145270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30586475 | GTCATTTTCAGTGAC[A/G]TTACTTCATAAATTG | 55632 |
rs183156009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567479 | ATTCTTTTTATTTGT[A/G]TTAGGTCTGTAGCAG | 55632 |
rs183176984 | snp | A/C/G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30569743 | GACCAGCTGGTGAAG[A/C/G/T]GGGGGGATTATATTA | 55632 |
rs183226747 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30585277 | AGATTTACCCTTATT[C/G]TTTCTGCTAAGAATT | 55632 |
rs183234044 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30572346 | GAGACTAAGGTGAAC[A/G]TTTGTAGATTCCCTT | 55632 |
rs183237340 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30604204 | GAATCAACCTGCTAT[A/T]AAAAAGGTATGTTTC | 55632 |
rs183477043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559331 | AGAAGCAGGACCGTG[A/G]GGTGGGAGAGGGTGT | 55632 |
rs183482033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30580092 | GTAAATGGTTGAGCA[C/T]TACCGTACTAGAAGA | 55632 |
rs183525153 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30599236 | CCTCTTTTTTTTGTT[G/T]GTTTGTTTTGAGATG | 55632 |
rs183532916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561186 | CACATACATTCTCTC[A/T]TTAATCTTTACAATA | 55632 |
rs183585467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30597241 | TAACCATTGGAAAAA[A/G]GAATTATAGATTTTA | 55632 |
rs183728519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577104 | GTGGCGTATGCCTGT[A/G]GTCCCAGCTACTCGG | 55632 |
rs183841461 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577262 | AAAGAAAAAATGTTG[C/G]GTGGTTAGGATCTGT | 55632 |
rs183885526 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30583729 | TAGCTGTTCCACAAT[A/G]TGTACATATATCAAA | 55632 |
rs183964024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566714 | GCTTTATTATTCTGA[A/G]TAGACCTTCTGGTTC | 55632 |
rs183964400 | snp | A/G | 0.00236408 | 0.0342995 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607999 | TTAACTGCCTTGTTT[A/G]TGGACCAGAAAATAC | 55632 |
rs183976393 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30560686 | TATTTTCATTGGATT[C/T]TTGCTCTTTCTTAAA | 55632 |
rs184006252 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620373 | TGTGATGGAACTGAA[A/G]TGGCTCAATGATGGA | 55632 |
rs184017688 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30597671 | AACCTTCTCCTCCCC[C/G]ACATGGCCAGTTCTT | 55632 |
rs184020536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594269 | TTAGTAACATCAAAT[A/G]TGTAATATGTACATG | 55632 |
rs184028301 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574470 | GTGAAGGTTTGTTAC[A/G]TAGGTAAACAACATG | 55632 |
rs184166705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614504 | CTCCCACAATAATGA[C/T]ATTAATCCATTTATG | 55632 |
rs184314342 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30588131 | GAAGTTGTCATTCCA[A/G]ATATGTTTATAAGTT | 55632 |
rs184354312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566076 | TAGTTTACTATAAAA[C/T]GTGAGTTTATTTATT | 55632 |
rs184423004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30583110 | GTTAGGGAGTTTCTG[C/T]GGTATGCAATCATTT | 55632 |
rs184466589 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592997 | TGACCTATTTAATGG[A/T]TTGTTATCATGTAAG | 55632 |
rs184590761 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619340 | AATACTAAGTCAAGG[A/G]GAGTATATTAGGTAA | 55632 |
rs184607063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30573855 | ACAGACACATCCAAA[C/T]ATAAGTTTAACCAGA | 55632 |
rs184709367 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30581960 | AAAATATTATTCTTA[A/C]AACTCTATATCTTGA | 55632 |
rs184817933 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30564757 | CCCTCATTTAATATA[A/G]TGTTTTCAAGGTTAT | 55632 |
rs184840888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605420 | TCTTTTTTTCCCCTC[A/G]TCTTGTTTTATTGGC | 55632 |
rs184856644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570284 | GTTTGACTATACTGT[G/T]TCTCAATGTGGATCT | 55632 |
rs184957378 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30613494 | AAGCTTTTTTGCTAT[A/G]TGGTATCACAAGGTG | 55632 |
rs184961259 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587682 | TTGGCCTCAATTTCT[C/T]CTAGCTAGCGTCAGG | 55632 |
rs184969567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562208 | GCCGAGGCAAGAGAC[C/T]GGGGGCACGAGCTGT | 55632 |
rs185047336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606898 | GCATATACTGTTGGG[A/T]GTAAACTTGTGCCTT | 55632 |
rs185152086 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30562586 | CCGCTACTTAGCAGA[C/G]CGGGAAAGGGAGTCT | 55632 |
rs185167908 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30579342 | CTTAATGGCATAGAA[A/T]ATTATTTTGTAAGGA | 55632 |
rs185224721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611269 | CAGGGATGAGGCAAC[A/G]TATACCCAATTATTA | 55632 |
rs185229562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585831 | CATAGGCTTGCATGA[C/G]CCTAAACATCAGCCA | 55632 |
rs185259437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602185 | TTGGAGAAAATTATG[A/G]TAGGAAATGCCATAT | 55632 |
rs185271454 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599507 | GCTGGGATTACAGGC[A/T]TGAGCCACTGCGCTC | 55632 |
rs185344339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561615 | AGCCATTGGCCTTTT[A/T]ATTTCCCCTTAAGAT | 55632 |
rs185397321 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30578301 | TTCAAGCTTAGAGAA[A/C]AGTTGTAAGAATGGC | 55632 |
rs185418353 | snp | A/C | 0.0174175 | 0.0916809 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558090 | GCTAATTTTTTGTAC[A/C]TTTAGTAGAGACGGG | 55632 |
rs185709190 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576552 | AAGGGTTTCTGCACA[A/G]CAAAAGAAACTACCA | 55632 |
rs185713720 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | G2E3 | GRCh38.p7 | 14:30601375 | AGCTTATTTTAGGAA[A/C]TATTCCTCACCTTGA | 55632 |
rs185716707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567390 | CTTGTCACTTTTGTT[A/G]TTTGTTTAACCTATT | 55632 |
rs185783951 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559066 | GAAGGGCGGGAGCAC[A/G]CGGGCCCTTCCCCAC | 55632 |
rs185798091 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596962 | TGTATTTGCTATAGC[A/G]ATGAGGATAGGTTTT | 55632 |
rs185801767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610791 | TTGTCTAGATTTTAG[A/G]GTAAGAGTTGGCAAA | 55632 |
rs185874182 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617657 | GAAAAACCCATTCTA[A/C]TGTCACCACTCAGAG | 55632 |
rs185892898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571677 | ATTGAATAGACTACC[A/G]TTTGAATACAGTGAA | 55632 |
rs186012435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591620 | TGGCAGCATAACTCC[A/G]ATCTGTTTCTATCTT | 55632 |
rs186040404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30616057 | TATACAATAAGTAGT[G/T]GTACTAAATGATTGT | 55632 |
rs186050864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589220 | TCAAACAATGTAAGT[A/G]GCCTCTTACTTTGAC | 55632 |
rs186060681 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30570677 | AGCTGCAGAATTTCT[A/G]TTTCCTTTTTATCAT | 55632 |
rs186129378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30595745 | AACTGAAATAACATA[C/T]GGAGTCTTATCCAAT | 55632 |
rs186258513 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616644 | TAGTTAGCTTCTTGA[C/G]CTAATAAAATTTATG | 55632 |
rs186271656 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576098 | AAAGCTGGAGGCATC[A/C]CATTACCCATCTTCA | 55632 |
rs186370977 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30584135 | AATATTGTGACCCTT[G/T]GTGTGTGTTTGACTT | 55632 |
rs186570093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610101 | GCATTTAAGACCTTC[A/G]CCTCTCTTCATGGCT | 55632 |
rs186574708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605330 | AAAACTAAGATTATC[A/G]AATAACTGTTTTTGG | 55632 |
rs186582698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30581780 | CTTCCCAAATAGATG[C/T]GGTCCGTTTTGACCT | 55632 |
rs186603134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30575470 | GAGAACCGACACAAG[A/G]CGAGGATACTCTCTC | 55632 |
rs186625051 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30567169 | TTCTGGCTTTGGTAT[C/G/T]GGGGTATTGGTGGCT | 55632 |
rs186781219 | snp | C/G | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30560939 | AACTGGGGCCAGATT[C/G]CCTTGGTTTGAAGCC | 55632 |
rs186791018 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557842 | ATAGCTTTACACACC[C/G]CCTGTGTCAGATTAC | 55632 |
rs186834441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30595061 | GAGAATCGCTTGAAC[C/T]CGGGAGGTAGAGGTT | 55632 |
rs186892927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563603 | GGAGCCAATGGGTGG[C/T]AGGGTGGGGTGGGGT | 55632 |
rs186946471 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30603807 | TATGATCATGCCACT[A/T]TACTCTCACCTGAGT | 55632 |
rs187022917 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618311 | ATAGCTAATATAAAC[C/T]CCAAAGTCACCATAC | 55632 |
rs187036241 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | G2E3 | GRCh38.p7 | 14:30561333 | AAGTTTATGCTTTTT[A/T]AAAAAAGTAATATTT | 55632 |
rs187068445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599400 | GCCTGGCTAATTTTT[C/G]TATTTTTTAGTAGAG | 55632 |
rs187075497 | snp | A/C | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577594 | GAATGGCCTCCATTC[A/C]TTACCAACTGGGTGT | 55632 |
rs187149178 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30579936 | CCTTGGTGAAGTGAA[A/G]CTTTAATGTTATTAA | 55632 |
rs187189754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591413 | AGCGGCACTGGTAGT[A/G]TATTCATTTCCTAGG | 55632 |
rs187412579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571429 | TTTCTTTGCTTAACT[A/G]TGTTTTTTTGATTAG | 55632 |
rs187435741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587118 | GGAGGTATTTCTTTT[A/G]CCACTTTCTTATTTC | 55632 |
rs187513768 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612603 | TCACTCACACCTGTA[A/G]TCCCAGCACTTCGGG | 55632 |
rs187583465 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577263 | AAGAAAAAATGTTGG[A/G]TGGTTAGGATCTGTT | 55632 |
rs187652825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30572069 | CATTTCTCTCAGCAG[C/T]GTTTTGTAGCTTTTC | 55632 |
rs187704988 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30567627 | ATTCTCAATTTAAAA[A/T]TTTTTTTATTACATT | 55632 |
rs187810091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606600 | GTATGGTGGAGAGTA[C/T]GTGAATTTAAATCAC | 55632 |
rs187839298 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30564864 | ATATCCATTCATCAA[C/T]TGATGTATAATTAGG | 55632 |
rs187840856 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30604665 | ACTATTTTAGGAATT[A/G]TGAATTCTGTTTATA | 55632 |
rs187843772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564552 | TTGTCCAGGCTGGTT[A/G]CAAACACCTAGCCTC | 55632 |
rs187848760 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30580237 | TTGAGATGGAGTTTC[A/G]CTGTTGTTGCCCAAG | 55632 |
rs187850830 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30564127 | TCACCCATTTTAGGG[G/T]TATAGTTCAATGAGT | 55632 |
rs188062349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30585958 | GGTTTTCCAAATTTT[C/T]ATTCCCTCATGTACC | 55632 |
rs188098433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582209 | CTTTATTTACATGAA[C/T]GTATTTAAGGTAGAA | 55632 |
rs188154038 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30573867 | AAACATAAGTTTAAC[C/G]AGATATCTGGGCGTC | 55632 |
rs188254687 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30609504 | TCTTTAATGCTTCTT[A/C]CTTCTTCTTACCCCT | 55632 |
rs188272406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568132 | AATTGTCATGTCTTC[C/T]TGATGGATTGAACTT | 55632 |
rs188334741 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30612005 | AAGTGGCATTATACT[A/C/T]TGGATTTCTTGAAGG | 55632 |
rs188362347 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30594794 | TTTTTTTTTTTTTGT[A/G]TGGACCTTGAACTTT | 55632 |
rs188370885 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30574550 | AATAGCCAATAGTTA[C/T]CTTTTCTGCTCCTCT | 55632 |
rs188578042 | snp | C/T | 1.66676e-05 | 0.00288679 | intron-variant | G2E3 | GRCh38.p7 | 14:30597544 | GAGTAACATTTAGCC[C/T]TATGATAAAAAAAAG | 55632 |
rs188616439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30598401 | CAAGAACAAAAAAAG[G/T]TTTTTATTTTTAGAT | 55632 |
rs188625073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560003 | AGTTCCACCGCCCTG[A/C]CTTTTCGCCTCCCTC | 55632 |
rs188844296 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30592544 | ATAAATTTTCTGTTT[A/G]GAGCATCAGAGTTTA | 55632 |
rs188894733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30616178 | GAGTCTGTGCCTTTC[A/G]GTATTCCAAGTCTAT | 55632 |
rs188902980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30589733 | TATTCCAACATGTCC[A/G]TCAGAATTGACCATC | 55632 |
rs188911178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571066 | GAAATTTTCTCCTCT[A/G]TGTTTTTTCTAGAAA | 55632 |
rs189114138 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618618 | AGACAGGGCCTTAGT[A/G]ATAAGATGGTGTAAA | 55632 |
rs189134702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30572423 | TTGTTATGATTGGAT[A/G]TTGACATTTGTCAGA | 55632 |
rs189147448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583800 | AAAGGATTAGTTGAG[G/T]CTTAACTCAGGTCTC | 55632 |
rs189276746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579116 | TAAACATCAAAAGCG[C/T]CATCGTATACCTGTA | 55632 |
rs189282893 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30613754 | ATGAGTGTGTCCTGA[G/T]AATTCTAATTCAGAT | 55632 |
rs189351440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562312 | TCATTAATCATTAGT[A/T]TGTAGCAATTACTCT | 55632 |
rs189366440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601748 | AACAAAATGTAAGTT[C/T]TGCTTTTCTTTGTGT | 55632 |
rs189371242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30566885 | TGTTTGAGTGTTTTT[A/G]TCATCAATGAGTTGT | 55632 |
rs189449092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593236 | TCAACATAATTATTA[C/G]TTTCTGAAATTCTGT | 55632 |
rs189456929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30610411 | CCGGGGTCAGCAGTT[C/T]GAGACCAGCCTGGCC | 55632 |
rs189502774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566298 | AGGCCATCGGGATTT[A/T]GACAGGAATTGTATC | 55632 |
rs189520545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583387 | TCATTTTTATGATGA[A/G]GAAATGGAGTCATAA | 55632 |
rs189607639 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30607254 | AAAGAGGTACAAGTA[C/T]AGTCATTTGTCACTT | 55632 |
rs189734518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588537 | TGAATATAATACTTT[A/T]AAAAAAAAGTACTGA | 55632 |
rs189778634 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558478 | CGATAAAGGAAAAGA[C/T]ACTGTTGTTTCAATA | 55632 |
rs189799571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596313 | CTGCTTTAATTTCAG[A/G]CACTCTTTTTGGTAG | 55632 |
rs189807438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576173 | TACAAAAACAGGCAC[A/G]TAGACCAGTGGAACA | 55632 |
rs189896699 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | G2E3 | GRCh38.p7 | 14:30570582 | ACCTGTCTTCAAGTT[C/T]GCTGATTCTTTCTCC | 55632 |
rs189974577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30578331 | CATAAGGAACTCCTA[C/T]ATATCCTTTATCTAG | 55632 |
rs190116018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597105 | GTTTCATTTTTTTCT[C/T]ACATTTTAAAGGGCA | 55632 |
rs190126339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576847 | AGATTAAAAAAATCA[A/G]TCAATTTCTCTTTCA | 55632 |
rs190147614 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561890 | TTCTGAGATGATAGC[A/G]TATAATTCTGTGTAG | 55632 |
rs190220451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600297 | CTGATTCCCTACTCT[A/G]GGCTAGGGGTTCCCT | 55632 |
rs190254709 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30570332 | TTAAAGATCTTGAGC[G/T]TCTTAAAAATGTGTA | 55632 |
rs190356713 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571787 | CTGACTTTTCCCTTA[G/T]GATCTATTGAGCTAC | 55632 |
rs190365516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30602474 | AGATCACTTTCAAGA[C/T]AGTTTGAAAAACACT | 55632 |
rs190371561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579837 | GGCATTATTATGTTT[G/T]ATTCTTTTCCACTTA | 55632 |
rs190456053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587691 | ATTTCTCCTAGCTAG[C/T]GTCAGGAAACCTCAG | 55632 |
rs190514852 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30595236 | GATCCTAGAGAGTGC[A/C]GTTAATAAACAACAT | 55632 |
rs190535887 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557989 | GCAATTTCTGCTCAC[C/T]GCAAGCTCCGTCTCC | 55632 |
rs190719715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30564291 | GGCTGCATCATATGA[C/T]AGGTGTACATTTGAC | 55632 |
rs190762892 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30581393 | AGAACAATTTAAACA[A/G]TGTGTAAAAGTTTAA | 55632 |
rs190773991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575838 | ATCTCTACAATGAGA[A/T]TTACAAAGCACTGCT | 55632 |
rs190814362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585834 | AGGCTTGCATGAGCC[C/T]AAACATCAGCCAGAG | 55632 |
rs190996215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30611023 | AGAGTTGTGATTTAC[A/G]AAACCGTCTAAGGAC | 55632 |
rs191001609 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585204 | TTTTTTCTTTTGTTA[C/T]CTGTGCTTTTAGTAT | 55632 |
rs191061105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30567437 | TTTAACTTCTTAGAG[C/T]ACAATTGTTCATAAT | 55632 |
rs191076608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567346 | ATTCAATCTCTTGTT[G/T]GTAGATTTGTTGAAA | 55632 |
rs191084921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567809 | TTTGACTTTTTGTCT[A/G]TTTAAAGTTGTTATT | 55632 |
rs191289544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591767 | AACTTAATTACATCT[G/T]CAAAGACCGTATTTC | 55632 |
rs191290134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599125 | GAGTTGTCCCTCTGT[C/T]GGTGTGTTGTCTACG | 55632 |
rs191301512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577394 | TGCTGGTTTTAAACA[A/G]TAAACATTTAATTAC | 55632 |
rs191320198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30584957 | CTTCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55632 |
rs191348008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562874 | TCTGCCTCGGCTGCC[A/G]GGCAGGGAAGGGCCC | 55632 |
rs191351289 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30561101 | AAAGACCTTAAAATA[A/G]TGTGTGCCACATAGC | 55632 |
rs191613666 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30599465 | AATGCCTGACCTCGT[G/T]ATCTGCCCGCCTCGG | 55632 |
rs191622955 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617682 | TCAGAGATAAGTACC[A/G]TATTTCTGTGTATCC | 55632 |
rs191628791 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580047 | TAGTGGAGAGTGAGG[A/G]GATAGGGACAGACCA | 55632 |
rs191641614 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569666 | CTGGTTATTTAGAGC[C/T]TGACTTGGTCAGTGG | 55632 |
rs191781429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30563966 | TCAAGGGATCTGCCC[A/G]CTTCAGCCTCCCAAA | 55632 |
rs191852930 | snp | A/T | 0.000431841 | 0.0146879 | intron-variant | G2E3 | GRCh38.p7 | 14:30593453 | TTCATGAGATTTTTT[A/T]AAAATAATTTACATT | 55632 |
rs191855158 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617278 | AAAACAGAATTGCAC[A/G]AATTTTCTGGAATCT | 55632 |
rs191857319 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574045 | AGTTGCAAGAAAAGT[A/T]CAAAGAACTACATAT | 55632 |
rs191864220 | snp | A/C/G | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30605338 | GATTATCAAATAACT[A/C/G]TTTTTGGTTCTAGTA | 55632 |
rs191873804 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30571581 | TTCTTGTGATCCAAT[A/T]TGAATTAAGTTTTAA | 55632 |
rs191913793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604101 | AAAGACGCTACACCA[A/G]GGAAGCTTGACTCCT | 55632 |
rs192128110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597603 | TGGAAATGATCACTT[A/G]TGTCTGATTCAGTGA | 55632 |
rs192167837 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618496 | GCTGATTAAGTCACA[A/C/G]ACACATACTTTGTTG | 55632 |
rs192169111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30591434 | ATTTCCTAGGGCTGC[C/T]ATAGCAAATTGGCTG | 55632 |
rs192177091 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592339 | AATGCTGTGTTTGCA[A/G]GAAAAATGGTGCTTC | 55632 |
rs192186792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30572247 | TTGGTAGGATTTTCT[A/G]TGTAGATGATCATAT | 55632 |
rs192415400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587734 | TGGGCCTCTTAGTAA[A/T]TAAGGCTACTCGTGG | 55632 |
rs192606442 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30570281 | TCAGTTTGACTATAC[G/T]GTGTCTCAATGTGGA | 55632 |
rs192659428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577699 | GGAGGAAGTCACAAT[A/G]CCTTTTATGACATTG | 55632 |
rs192664700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30612869 | CTCAAAAAAATGAAA[A/G]AAGAATTGTGTAAAT | 55632 |
rs192667886 | snp | A/G/T | 6.60954e-05 | 0.00574838 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612243 | GCTGACTTAAAGTCA[A/G/T]TAATAAATGAATGCT | 55632 |
rs192674481 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30587363 | CCTCCACCAATTTCT[C/T]ACCTCACTGAATTCA | 55632 |
rs192755821 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564660 | ATTTTAAAGTAGACA[C/T]TTCAGTGACAGTACA | 55632 |
rs192760401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614122 | AGTATATACAAAGAA[A/G]TATAGGTTTCATCCT | 55632 |
rs192763062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570445 | TGTTCCACTTTCTCC[A/G]GTCCCTCTTGGACTC | 55632 |
rs192841391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30586043 | TATCTGTTATCCCTT[A/G]TCCTAGGCTGCTACA | 55632 |
rs192888407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561402 | AAGTATCTCTGATGG[C/T]TTCTCATTGTCTACC | 55632 |
rs192908120 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30582865 | ACTATATTAAATACG[A/C]GCTCATCTTATTTCT | 55632 |
rs192987812 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | G2E3 | GRCh38.p7 | 14:30620035 | TCTAATGTAAAATAG[C/T]TTACCAGAATAAATT | 55632 |
rs193006093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581801 | GTTTTGACCTTTGCT[A/T]TTAATTGTTGTTTTC | 55632 |
rs193028378 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572637 | TTTTCACCCCTTATT[A/G/T]TATTAACATGGTGTA | 55632 |
rs193150630 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30560026 | CCTCCCTCATTCATT[A/G]GCCAACTGGGTTATT | 55632 |
rs193175364 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565499 | GCTTTTGGTGTCATA[A/T]CTCAGAAACCATTGC | 55632 |
rs193239982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30592591 | TATTACCCTCCCGCC[C/T]ACCCTTATGGGGTCA | 55632 |
rs199518352 | in-del | -/TCGTTTATATGTCAGCCTATTTC | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619726 | TATTATGCTAGGTGA[-/TCGTTTATATGTCAGCCTATTTC]CCCCCCTTTTAAAGA | 55632 |
rs199562965 | in-del | -/AAC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574422 | TCATCTTTTTTTTTT[-/AAC]TTTTTTTTTTTTTTA | 55632 |
rs199616266 | snp | C/T | 0.00199798 | 0.0315436 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586752 | ACATGATGACTGTCC[C/T]AATAAATACGGAGAA | 55632 |
rs199779040 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | G2E3 | GRCh38.p7 | 14:30597929 | AAGTGAAATATTTGG[-/A]AAAAATGTGTTATAA | 55632 |
rs199788823 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617945 | AGTAAATCATTATGG[G/T]AAGTAAAATGTTTTA | 55632 |
rs199834656 | snp | C/T | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592362 | GGTGCTTCAATTGGA[C/T]GTGTTGCACCCCGAT | 55632 |
rs199858242 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608990 | TGTCTCAAAAAAAAA[-/A]GCACAGGCTTGGAAG | 55632 |
rs199884519 | in-del | -/T | 0.117886 | 0.21224 | intron-variant | G2E3 | GRCh38.p7 | 14:30606238 | CTTTTGTTTGCAATA[-/T]TTTTTTTTTTTGCAC | 55632 |
rs199950088 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603370 | TAAGTTACTTTCAAA[A/G]TCTTAAACATTTAAA | 55632 |
rs199986859 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619749 | ATGTCAGCCTATTTC[A/C]CCCCCTTTTAAAGAC | 55632 |
rs200018823 | in-del | -/AT | 0.0209421 | 0.100162 | intron-variant | G2E3 | GRCh38.p7 | 14:30593860 | AGATGAAACTTTTTA[-/AT]ATGTATATTTATACT | 55632 |
rs200033601 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581985 | TCTTGATCATTACTT[C/T]TAAAGTATCTTTTGA | 55632 |
rs200057461 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573430 | GTGTGTGTGTGTGTG[C/T]GCGTGTGTGTGTGTC | 55632 |
rs200120983 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573437 | TGTGTGTGTGCGTGT[C/G]TGTGTGTCTCTGTGT | 55632 |
rs200128131 | snp | C/T | 0.000115918 | 0.0076122 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602032 | AAAAACATGTATTAC[C/T]CAATTCTAATAATGT | 55632 |
rs200219517 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613698 | TTTTAATCTATTTTG[-/T]TTTTTTTTTTTAAAA | 55632 |
rs200264848 | snp | C/T | | | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592358 | AAATGGTGCTTCAAT[C/T]GGATGTGTTGCACCC | 55632 |
rs200299891 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612615 | GTAATCCCAGCACTT[C/T]GGGAGGCTGGGGCAG | 55632 |
rs200307535 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609654 | TTTATATACAGATAA[-/G]GACCTGGGTCTTGCT | 55632 |
rs200321646 | in-del | -/TT | 0.0146672 | 0.084371 | intron-variant | G2E3 | GRCh38.p7 | 14:30586953 | CTCTAAAAATAGACA[-/TT]TTGTTTTTTGATATT | 55632 |
rs200400212 | snp | C/T | 8.41338e-05 | 0.00648535 | intron-variant | G2E3 | GRCh38.p7 | 14:30607867 | GAAGTGTATTTGATA[C/T]ATTTTCATCTGTATT | 55632 |
rs200478667 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566997 | TTGGTTGATTTCCAT[A/G]TGCTGAACCACCTTT | 55632 |
rs200593420 | in-del | -/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577238 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAGAAA | 55632 |
rs200656938 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577244 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAATGT | 55632 |
rs200666506 | in-del | -/T | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618368 | AAAGATATTTGTTTC[-/T]TTATCCACCTTATTT | 55632 |
rs200672015 | in-del | -/AA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588245 | ATTTTACTTTTCTAT[-/AA]AAAGTAAAAGGATTA | 55632 |
rs200693428 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593569 | TGGAATTTATTGAGC[C/T]TATTCCAAGTTATAA | 55632 |
rs200707201 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599233 | TTACCTCTTTTTTTT[-/G]TTTGTTTGTTTTGAG | 55632 |
rs200747829 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617947 | TAAATCATTATGGGA[A/G]GTAAAATGTTTTAAC | 55632 |
rs200767722 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613710 | TTTGTTTTTTTTTTT[-/A]AAATCAAACTTTTTT | 55632 |
rs200781968 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565136 | CATCATTAACACTTA[A/C]TATTTTAGTTTGTAA | 55632 |
rs200872914 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618040 | ATCATTACATTATTG[A/G]TATTTTTTAAGTAAC | 55632 |
rs200886727 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant | G2E3 | GRCh38.p7 | 14:30581701 | GCGAGACCCTGTATC[-/A]AAAAAAAAGAAGAAA | 55632 |
rs201063340 | in-del | -/CATT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604910 | ATTCATTCATTCATT[-/CATT]TATGAGACGGAGTTT | 55632 |
rs201105709 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594791 | CCTTTTTTTTTTTTT[-/T]GTATGGACCTTGAAC | 55632 |
rs201121201 | in-del | -/TGT | 0.0861826 | 0.188849 | intron-variant | G2E3 | GRCh38.p7 | 14:30596091 | GAGATTTCAATAACC[-/TGT]TGTTTCCCTCCCTTA | 55632 |
rs201124698 | snp | C/G | 0.000101341 | 0.0071176 | intron-variant | G2E3 | GRCh38.p7 | 14:30601964 | AGTTTTTACCTATAT[C/G]TCTATTATGCTAACA | 55632 |
rs201146218 | in-del | -/ATA | 0.0150606 | 0.0854603 | intron-variant | G2E3 | GRCh38.p7 | 14:30607191 | TAAAAAGTTTACAAT[-/ATA]ATAAGTGGATAAAGC | 55632 |
rs201265829 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617944 | AAGTAAATCATTATG[A/G]GAAGTAAAATGTTTT | 55632 |
rs201308683 | in-del | -/AAT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587733 | CTGGGCCTCTTAGTA[-/AAT]AAGGCTACTCGTGGC | 55632 |
rs201315670 | in-del | -/AG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586268 | ACACGGGCCACCCCA[-/AG]ACCACTGCCCAGCTG | 55632 |
rs201316250 | snp | A/G | 0.00284386 | 0.0376011 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605673 | TGCAATTGAAGTAGC[A/G]TATGTTATTGAAAAT | 55632 |
rs201340511 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580033 | TTTATTTGTTTAACT[A/G]GTGGAGAGTGAGGAG | 55632 |
rs201360494 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30592612 | TATGGGGTCATTTCT[C/T]TGTGCCAAGTCTTGA | 55632 |
rs201373923 | snp | A/T | 1.69137e-05 | 0.00290802 | intron-variant | G2E3 | GRCh38.p7 | 14:30601942 | ATTCAAATGTATATG[A/T]TTTAAAAGTTTTTAC | 55632 |
rs201440879 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560089 | TTTGAGCATCTGTTT[C/T]TTTGGGTTTTATTGT | 55632 |
rs201506583 | snp | A/G | 0.000122278 | 0.00781819 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586789 | ACTAAGGAGAAATGG[A/G]ATCTCACTGTACATT | 55632 |
rs201511939 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612625 | CACTTCGGGAGGCTG[A/G]GGCAGGCAGATCATT | 55632 |
rs201545564 | snp | C/T | 0.000100935 | 0.00710334 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593533 | ATAATTATAGAGAGT[C/T]CTTACCATGCACCAT | 55632 |
rs201630875 | in-del | -/TG | 0.0422008 | 0.138995 | intron-variant | G2E3 | GRCh38.p7 | 14:30599760 | GGAAATAAAAATATA[-/TG]TTATTTAACTTTTTT | 55632 |
rs201634498 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611446 | TTAATGGATTGTTTC[C/G]TATTTTTAACTTTCT | 55632 |
rs201655816 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573435 | TGTGTGTGTGTGCGT[C/G]TGTGTGTGTCTCTGT | 55632 |
rs201665260 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560111 | TTTTATTGTTTTGGG[C/T]TTTTTTTTTTTTAAT | 55632 |
rs201772853 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577698 | AGGAGGAAGTCACAA[C/T]GCCTTTTATGACATT | 55632 |
rs201823924 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563023 | CTCCGTGTCTTGGTG[A/G]TAGTGGTCCCCCGGG | 55632 |
rs201932225 | in-del | -/TGTGTGTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563696 | TAACTTTGTTACTTT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 55632 |
rs201949276 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585924 | GTGGACTTCTAGATT[A/C]TCCAGTTATTATGCA | 55632 |
rs201967382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581149 | AAATAATTTTATTAC[A/C]ATGAGTGTTTTAAAT | 55632 |