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 |